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  • 1. Abdelhalim, Mohamed A.
    et al.
    Tenorio, Emanuel R.
    Oderich, Gustavo S.
    Haulon, Stephan
    Warren, Gasper
    Adam, Donald
    Claridge, Martin
    Butt, Talha
    Abisi, Said
    Dias, Nuno V.
    Kölbel, Tilo
    Gallitto, Enrico
    Gargiulo, Mauro
    Gkoutzios, Panos
    Panuccio, Giuseppe
    Kuzniar, Marek
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Mani, Kevin
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Mees, Barend M.
    Schurink, Geert W.
    Sonesson, Björn
    Spath, Paolo
    Wanhainen, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Schanzer, Andres
    Beck, Adam W.
    Schneider, Darren B.
    Timaran, Carlos H.
    Eagleton, Matthew
    Farber, Mark A.
    Modarai, Bijan
    Multicenter trans-Atlantic experience with fenestrated-branched endovascular aortic repair of chronic post-dissection thoracoabdominal aortic aneurysms2023In: Journal of Vascular Surgery, ISSN 0741-5214, E-ISSN 1097-6809, Vol. 78, no 4, p. 854-862.e1Article in journal (Refereed)
    Abstract [en]

    OBJECTIVE: This multicenter international study aimed to describe outcomes of fenestrated-branched endovascular aortic repairs (FB-EVAR) in a cohort of patients treated for chronic post-dissection thoracoabdominal aortic aneurysms (PD-TAAAs).

    METHODS: We reviewed the clinical data of all consecutive patients treated by FB-EVAR for repair of extent I to III PD-TAAAs in 16 centers from the United States and Europe (2008-2021). Data were extracted from institutional prospectively maintained databases and electronic patient records. All patients received off-the-shelf or patient-specific manufactured fenestrated-branched stent grafts. Endpoints were any cause mortality and major adverse events at 30 days, technical success, target artery (TA) patency, freedom from TA instability, minor (endovascular with <12 Fr sheath) and major (open or ≥12 Fr sheath) secondary interventions, patient survival, and freedom from aortic-related mortality (ARM).

    RESULTS: A total of 246 patients (76% male; median age, 67 years [interquartile range, 61-73 years]) were treated for extent I (7%), extent II (55%), and extent III (35%) PD-TAAAs by FB-EVAR. The median aneurysm diameter was 65 mm (interquartile range, 59-73 mm). Eighteen patients (7%) were octogenarians, 212 (86%) were American Society of Anesthesiologists class ≥3, and 21 (9%) presented with contained ruptured or symptomatic aneurysms. There were 917 renal-mesenteric vessels targeted by 581 fenestrations (63%) and 336 directional branches (37%), with a mean of 3.7 vessels per patient. Technical success was 96%. Mortality and rate of major adverse events at 30 days was 3% and 28%, including disabling complications such as new onset dialysis in 1%, major stroke in 1%, and permanent paraplegia in 2%. Mean follow-up was 24 months. Kaplan-Meier (KM) estimated patient survival at 3 and 5 years was 79% ± 6% and 65% ± 10%. KM estimated freedom from ARM was 95% ± 3% and 93% ± 5% at the same intervals. Unplanned secondary interventions were needed in 94 patients (38%), including minor procedures in 64 (25%) and major procedures in 30 (12%). There was one conversion to open surgical repair (<1%). KM estimated freedom from any secondary intervention was 44% ± 9% at 5 years. KM estimated primary and secondary TA patency were 93% ± 2% and 96% ± 1% at 5 years, respectively.

    CONCLUSIONS: FB-EVAR for chronic PD-TAAAs was associated with high technical success and a low rate of mortality (3%) and disabling complications at 30 days. Although the procedure is effective in the prevention of ARM, patient survival was low at 5 years (65%), likely due to the significant comorbidities in this cohort of patients. Freedom from secondary interventions at 5 years was 44%, although most procedures were minor. The significant rate of reinterventions highlights the need for continued patient surveillance.

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  • 2. Acosta, S.
    et al.
    Bjarnason, T.
    Petersson, U.
    Pålsson, B.
    Wanhainen, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Svensson, M.
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Djavani, Khatereh
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Björck, Martin
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Multicentre prospective study of fascial closure rate after open abdomen with vacuum and mesh-mediated fascial traction2011In: British Journal of Surgery, ISSN 0007-1323, E-ISSN 1365-2168, Vol. 98, no 5, p. 735-743Article in journal (Refereed)
    Abstract [en]

    Background: Damage control surgery and temporary open abdomen (OA) have been adopted widely, in both trauma and non-trauma situations. Several techniques for temporary abdominal closure have been developed. The main objective of this study was to evaluate the fascial closure rate in patients after vacuum-assisted wound closure and mesh-mediated fascial traction (VAWCM) for long-term OA treatment, and to describe complications. Methods: This prospective study included all patients who received VAWCM treatment between 2006 and 2009 at four hospitals. Patients with anticipated OA treatment for fewer than 5 days and those with non-midline incisions were excluded. Results: Among 151 patients treated with an OA, 111 received VAWCM treatment. Median age was 68 years. Median OA treatment time was 14 days. Main disease aetiologies were vascular (45 patients), visceral surgical disease (57) and trauma (9). The fascial closure rate was 76.6 per cent in intention-to-treat analysis and 89 per cent in per-protocol analysis. Eight patients developed an intestinal fistula, of whom seven had intestinal ischaemia. Intestinal fistula was an independent factor associated with failure of fascial closure (odds ratio (OR) 8.55, 95 per cent confidence interval 1.47 to 49.72; P = 0.017). The in-hospital mortality rate was 29.7 per cent. Age (OR 1.21, 1.02 to 1.43; P = 0.027) and failure of fascial closure (OR 44.50, 1.13 to 1748.52; P = 0.043) were independently associated with in-hospital mortality. Conclusion: The VAWCM method provided a high fascial closure rate after long-term treatment of OA. Technique-related complications were few. No patient was left with a large planned ventral hernia.

  • 3.
    Acosta, S.
    et al.
    Lund Univ, Dept Clin Sci, Vasc Ctr, Malmo, Sweden..
    Björck, Martin
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Wanhainen, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Negative-pressure wound therapy for prevention and treatment of surgical-site infections after vascular surgery2017In: British Journal of Surgery, ISSN 0007-1323, E-ISSN 1365-2168, Vol. 104, no 2, p. E75-E84Article, review/survey (Refereed)
    Abstract [en]

    BackgroundIndications for negative-pressure wound therapy (NPWT) in vascular surgical patients are expanding. The aim of this review was to outline the evidence for NPWT on open and closed wounds. MethodsA PubMed, EMBASE and Cochrane Library search from 2007 to June 2016 was performed combining the medical subject headings terms wound infection', abdominal aortic aneurysm (AAA)', fasciotomy', vascular surgery' and NPWT' or VAC'. ResultsNPWT of open infected groin wounds was associated with shorter duration of wound healing by 47 days, and was more cost-effective than alginate dressings in one RCT. In one RCT and six observational studies, NPWT-related major bleeding and graft preservation rates were 0-10 and 83-100 per cent respectively. One retrospective comparative study showed greater wound size reduction per day, fewer dressing changes, quicker wound closure and shorter hospital stay with NPWT compared with gauze dressings for lower leg fasciotomy. NPWT and mesh-mediated fascial traction after AAA repair and open abdomen was associated with high primary fascial closure rates (96-100 per cent) and low risk of graft infection (0-7 per cent). One retrospective comparative study showed a significant reduction in surgical-site infection, from 30 per cent with standard wound care to 6 per cent with closed incisional NPWT. ConclusionNPWT has a central role in open and infected wounds after vascular surgery; the results of prophylactic care of closed incisions are promising.

  • 4.
    Acosta, S.
    et al.
    Lund Univ, Vasc Ctr, Dept Clin Sci, Malmo, Sweden..
    Wanhainen, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Björck, Martin
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Temporary Abdominal Closure After Abdominal Aortic Aneurysm Repair: A Systematic Review of Contemporary Observational Studies2016In: European Journal of Vascular and Endovascular Surgery, ISSN 1078-5884, E-ISSN 1532-2165, Vol. 51, no 3, p. 371-378Article, review/survey (Refereed)
    Abstract [en]

    Objectives: The aim of this paper was to review the literature on temporary abdominal closure (TAC) after abdominal aortic aneurysm (AAA) repair. Methods: This was a systematic review of observational studies. A PubMed, EM BASE and Cochrane search from 2007 to July 2015 was performed combining the Medical Subject Headings "aortic aneurysm" and "temporary abdominal closure", "delayed abdominal closure", "open abdomen", "abdominal compartment syndrome", "negative pressure wound therapy", or "vacuum assisted wound closure". Results: Seven original studies were found. The methods used for TAC were the vacuum pack system with (n = 1) or without (n = 2) mesh bridge, vacuum assisted wound closure (VAWC; n = 1) and the VAWC with mesh mediated fascial traction (VACM; n = 3). The number of patients included varied from four to 30. Three studies were exclusively after open repair, one after endovascular aneurysm repair, and three were mixed series. The frequency of ruptured AAA varied from 60% to 100%. The primary fascia] closure rate varied from 79% to 100%. The median time to closure of the open abdomen was 10.5 and 17 days in two prospective studies with a fascia] closure rate of 100% and 96%, respectively; the inclusion criterion was an anticipated open abdomen therapy time >= 5 days using the VACM method. The graft infection rate was 0% in three studies. No patient with longterm open abdomen therapy with the VACM in the three studies was left with a planned ventral hernia. The in hospital survival rate varied from 46% to 80%. Conclusions: A high fascial closure rate without planned ventral hernia is possible to achieve with VACM, even after long-term open abdomen therapy. There are, however, few publications reporting specific results of open abdomen treatment after AAA repair, and there is a need for randomized controlled trials to determine the most efficient and safe TAC method during open abdomen treatment after AAA repair.

  • 5. Acosta, Stefan
    et al.
    Seternes, Arne
    Venermo, Maarit
    Vikatmaa, Leena
    Sörelius, Karl
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Wanhainen, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Svensson, Mats
    Djavani, Khatereh
    Department of Surgery, Gävle Hospital, Gävle, Sweden.
    Björck, Martin
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Open Abdomen Therapy with Vacuum and Mesh Mediated Fascial Traction After Aortic Repair: an International Multicentre Study2017In: European Journal of Vascular and Endovascular Surgery, ISSN 1078-5884, E-ISSN 1532-2165, Vol. 54, no 6, p. 697-705Article in journal (Refereed)
    Abstract [en]

    OBJECTIVES:

    Open abdomen therapy may be necessary to prevent or treat abdominal compartment syndrome (ACS). The aim of the study was to analyse the primary delayed fascial closure (PDFC) rate and complications after open abdomen therapy with vacuum and mesh mediated fascial traction (VACM) after aortic repair and to compare outcomes between those treated with open abdomen after primary versus secondary operation.

    METHODS:

    This was a retrospective cohort, multicentre study in Sweden, Finland, and Norway, including consecutive patients treated with open abdomen and VACM after aortic repair at six vascular centres in 2006-2015. The primary endpoint was PDFC rate.

    RESULTS:

    Among 191 patients, 155 were men. The median age was 71 years (IQR 66-76). Ruptured abdominal aortic aneurysm (RAAA) occurred in 69.1%. Endovascular/hybrid and open repairs were performed in 49 and 142 patients, respectively. The indications for open abdomen were inability to close the abdomen (62%) at primary operation and ACS (80%) at secondary operation. Duration of open abdomen was 11 days (IQR 7-16) in 157 patients alive at open abdomen termination. The PDFC rate was 91.8%. Open abdomen initiated at primary (N=103), compared with secondary operation (N=88), was associated with less severe initial open abdomen status (p=.006), less intestinal ischaemia (p=.002), shorter duration of open abdomen (p=.007), and less renal replacement therapy (RRT, p<.001). In hospital mortality was 39.3%, and after entero-atmospheric fistula (N=9) was 88.9%. Seven developed graft infection within 6 months, 1 year mortality was 28.6%. Intestinal ischaemia (OR 3.71, 95% CI 1.55-8.91), RRT (OR 3.62, 95% CI 1.72-7.65), and age (OR 1.12, 95% CI 1.06-1.12), were independent factors associated with in hospital mortality, but not open abdomen initiated at primary versus secondary operation.

    CONCLUSIONS:

    VACM was associated with a high PDFC rate after prolonged open abdomen therapy following aortic repair. Patient outcomes seemed better when open abdomen was initiated at primary, compared with secondary operation but a selection effect is possible.

  • 6.
    Antoni, Gunnar
    et al.
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Pharmacy, Department of Medicinal Chemistry, Preparative Medicinal Chemistry.
    Lubberink, Mark
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Radiology.
    Sörensen, Jens
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Radiology.
    Lindström, Elin
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Radiology.
    Elgland, Mathias
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Pharmacy, Department of Medicinal Chemistry.
    Eriksson, Olof
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Pharmacy, Department of Medicinal Chemistry, Translational PET Imaging.
    Hultström, Michael
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Anaesthesiology and Intensive Care.
    Frithiof, Robert
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Anaesthesiology and Intensive Care.
    Wanhainen, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Sigfridsson, Jonathan
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Radiology.
    Skorup, Paul
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Medical Sciences, Infection medicine.
    Lipcsey, Miklos
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Anaesthesiology and Intensive Care.
    In Vivo Visualization and Quantification of Neutrophil Elastase in Lungs of COVID-19 Patients: A First-in-Humans PET Study with 11C-NES2023In: Journal of Nuclear Medicine, ISSN 0161-5505, E-ISSN 1535-5667, Vol. 64, no 1, p. 145-148Article in journal (Refereed)
    Abstract [en]

    COVID-19 can cause life-threatening lung-inflammation that is suggested to be mediated by neutrophils, whose effector mechanisms in COVID-19 is inexplicit. The aim of the present work is to evaluate a novel PET tracer for neutrophil elastase in COVID-19 patients and healthy controls.

    METHODS: In this open-label, First-In-Man study, four patients with hypoxia due to COVID-19 and two healthy controls were investigated with positron emission tomography (PET) using the new selective and specific neutrophil elastase PET-tracer [11C]GW457427 and [15O]water for the visualization and quantification of NE and perfusion in the lungs, respectively.

    RESULTS: [11C]GW457427 accumulated selectively in lung areas with ground-glass opacities on computed tomography characteristic of COVID-19 suggesting high levels on NE in these areas. In the same areas perfusion was severely reduced in comparison to healthy lung tissue as measured with [15O]water.

    CONCLUSION: The data suggests that NE may be responsible for the severe lung inflammation in COVID-19 patients and that inhibition of NE could potentially reduce the acute inflammatory process and improve the condition.

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  • 7.
    Antoniou, George A.
    et al.
    Department of Vascular and Endovascular Surgery, Manchester University NHS Foundation Trust, Manchester, UK; Division of Cardiovascular Sciences, School of Medical Sciences, Manchester Academic Health Science Centre, The University of Manchester, Manchester, UK .
    Bastos Gonçalves, Frederico
    Centro Hospitalar Universitário de Lisboa Central, Lisbon, Portugal; NOVA Medical School, Universidade NOVA de Lisboa, Portuga.
    Björck, Martin
    Department of Surgical Sciences, Section of Vascular Surgery, Uppsala University, Uppsala, Sweden.
    Chakfé, Nabil
    Groupe Européen de Recherche sur les Prothèses Appliquées à la Chirurgie Vasculaire, Strasbourg, France; Department of Vascular Surgery and Kidney Transplantation, University Hospital of Strasbourg, France.
    Coscas, Raphaël
    Department of Vascular Surgery, Ambroise Paré University Hospital, Assistance Publique - Hôpitaux de Paris (AP-HP), Boulogne-Billancourt, France; Faculté de Médecine Paris-Ile de France-Ouest, UFR des sciences de la santé Simone Veil, Université Versailles Saint-Quentin en Yvelines, Montigny-le-Bretonneux, France.
    Dias, Nuno V.
    Vascular Centre, Skåne University Hospital, Malmö, Sweden.
    Dick, Florian
    Department of Vascular Surgery, Kantonsspital St. Gallen, University of Bern, Bern, Switzerland.
    Kakkos, Stavros K.
    Department of Vascular Surgery, University of Patras Medical School, Patras, Greece.
    Mees, Barend M.E.
    Department of Vascular Surgery, Maastricht University Medical Centre and CARIM School for Cardiovascular Diseases, Maastricht University, Maastricht, Netherlands.
    Resch, Timothy
    Department of Vascular Surgery, Copenhagen University Hospital- Rigshospitalet, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
    Trimarchi, Santi
    Vascular Surgery, Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, Milan, Italy; Department of Clinical Sciences and Community Health, Università degli Studi di Milano, Milan, Italy.
    Tulamo, Riikka
    Department of Vascular Surgery, Helsinki University Hospital, University of Helsinki, Helsinki, Finland.
    Twine, Chris P.
    Department of Vascular Surgery, North Bristol NHS Trust, UK, Bristol, United Kingdom; Centre for Surgical Research, University of Bristol, UK, Bristol, United Kingdom.
    Vermassen, Frank
    Department of Thoracic and Vascular Surgery, Ghent University Hospital, Ghent, Belgium.
    Wanhainen, Anders
    Umeå University, Faculty of Medicine, Department of Surgical and Perioperative Sciences, Surgery. Department of Surgical Sciences, Section of Vascular Surgery, Uppsala University, Uppsala, Sweden.
    Kolh, Philippe
    Department of Biomedical and Preclinical Sciences, University of Liège, Belgium; GIGA Cardiovascular Sciences, University of Liège, Belgium; Department of Information System Management, University Hospital of Liège, Belgium.
    European society for vascular surgery clinical practice guideline development scheme: an overview of evidence quality assessment methods, evidence to decision frameworks, and reporting standards in guideline development2022In: European Journal of Vascular and Endovascular Surgery, ISSN 1078-5884, E-ISSN 1532-2165, Vol. 63, no 6, p. 791-799Article, review/survey (Refereed)
    Abstract [en]

    Objective: A structured and transparent approach is instrumental in translating research evidence to health recommendations and evidence informed clinical decisions. The aim was to conduct an overview and analysis of principles and methodologies for health guideline development.

    Methods: A literature review on methodologies, strategies, and fundamental steps in the process of guideline development was performed. The clinical practice guideline development process and methodology adopted by the European Society for Vascular Surgery are also presented.

    Results: Sophisticated methodologies for health guideline development are being applied increasingly by national and international organisations. Their overarching principle is a systematic, structured, transparent, and iterative process that is aimed at making well informed healthcare choices. Critical steps in guideline development include the assessment of the certainty of the body of evidence; evidence to decision frameworks; and guideline reporting. The goal of strength of evidence assessments is to provide well reasoned judgements about the guideline developers’ confidence in study findings, and several evidence hierarchy schemes and evidence rating systems have been described for this purpose. Evidence to decision frameworks help guideline developers and users conceptualise and interpret the construct of the quality of the body of evidence. The most widely used evidence to decision frameworks are those developed by the GRADE Working Group and the WHO-INTEGRATE, and are structured into three distinct components: background; assessment; and conclusions. Health guideline reporting tools are employed to ensure methodological rigour and transparency in guideline development. Such reporting instruments include the AGREE II and RIGHT, with the former being used for guideline development and appraisal, as well as reporting.

    Conclusion: This guide will help guideline developers/expert panels enhance their methodology, and patients/clinicians/policymakers interpret guideline recommendations and put them in context. This document may be a useful methodological summary for health guideline development by other societies and organisations.

  • 8.
    Antoniou, George A.
    et al.
    Manchester Univ NHS Fdn Trust, Dept Vasc & Endovasc Surg, Manchester, Lancs, England.;Univ Manchester, Manchester Acad Hlth Sci Ctr, Sch Med Sci, Div Cardiovasc Sci, Manchester, Lancs, England..
    Goncalves, Frederico Bastos
    Ctr Hosp Univ Lisboa Cent, Lisbon, Portugal.;Univ NOVA Lisboa, NOVA Med Sch, Lisbon, Portugal..
    Björck, Martin
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Chakfe, Nabil
    Grp Europeen Rech Protheses Appl Chirurg Vasc, Strasbourg, France.;Univ Hosp Strasbourg, Dept Vasc Surg & Kidney Transplantat, Strasbourg, France..
    Coscas, Raphael
    Ambroise Pare Univ Hosp, Assistance Publ Hop Paris AP HP, Dept Vasc Surg, Boulogne, France.;Univ Versailles St Quentin En Yvelines, UFR Sci Sante Simone Veil, Fac Med Paris Ile France Ouest, Montigny Le Bretonneux, France..
    Dias, Nuno, V
    Skane Univ Hosp, Vasc Ctr, Malmö, Sweden..
    Dick, Florian
    Univ Bern, Kantonsspital St Gallen, Dept Vasc Surg, Bern, Switzerland..
    Kakkos, Stavros K.
    Univ Patras Med Sch, Dept Vasc Surg, Patras, Greece..
    Mees, Barend M. E.
    Maastricht Univ, Dept Vasc Surg, Maastricht Univ Med Ctr, Maastricht, Netherlands.;Maastricht Univ, CARIM Sch Cardiovasc Dis, Maastricht, Netherlands..
    Resch, Timothy
    Univ Copenhagen, Fac Hlth & Med Sci, Rigshosp, Dept Vasc Surg,Copenhagen Univ Hosp, Copenhagen, Denmark..
    Trimarchi, Santi
    IRCCS Ca Granda Osped Maggiore Policlin, Vasc Surg, Milan, Italy.;Univ Milan, Dept Clin Sci & Community Hlth, Milan, Italy..
    Tulamo, Riikka
    Univ Helsinki, Helsinki Univ Hosp, Dept Vasc Surg, Helsinki, Finland..
    Twine, Chris P.
    North Bristol NHS Trust, Dept Vasc Surg, Bristol, Avon, England.;Univ Bristol, Ctr Surg Res, Bristol, Avon, England..
    Vermassen, Frank
    Ghent Univ Hosp, Dept Thorac & Vasc Surg, Ghent, Belgium..
    Wanhainen, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery. Umeå Univ, Dept Surg & Perioperat Sci, Umeå, Sweden..
    Kolh, Philippe
    Univ Liege, Dept Biomed & Preclin Sci, Liege, Belgium.;Univ Liege, GIGA Cardiovasc Sci, Liege, Belgium.;Univ Hosp Liege, Dept Informat Syst Management, Liege, Belgium..
    European Society for Vascular Surgery Clinical Practice Guideline Development Scheme: An Overview of Evidence Quality Assessment Methods, Evidence to Decision Frameworks, and Reporting Standards in Guideline Development2022In: European Journal of Vascular and Endovascular Surgery, ISSN 1078-5884, E-ISSN 1532-2165, Vol. 63, no 6, p. 791-799Article in journal (Refereed)
    Abstract [en]

    Objective: A structured and transparent approach is instrumental in translating research evidence to health recommendations and evidence informed clinical decisions. The aim was to conduct an overview and analysis of principles and methodologies for health guideline development.

    Methods: A literature review on methodologies, strategies, and fundamental steps in the process of guideline development was performed. The clinical practice guideline development process and methodology adopted by the European Society for Vascular Surgery are also presented.

    Results: Sophisticated methodologies for health guideline development are being applied increasingly by national and international organisations. Their overarching principle is a systematic, structured, transparent, and iterative process that is aimed at making well informed healthcare choices. Critical steps in guideline development include the assessment of the certainty of the body of evidence; evidence to decision frameworks; and guideline reporting. The goal of strength of evidence assessments is to provide well reasoned judgements about the guideline developers' confidence in study findings, and several evidence hierarchy schemes and evidence rating systems have been described for this purpose. Evidence to decision frameworks help guideline developers and users conceptualise and interpret the construct of the quality of the body of evidence. The most widely used evidence to decision frameworks are those developed by the GRADE Working Group and the WHO-INTEGRATE, and are structured into three distinct components: background; assessment; and conclusions. Health guideline reporting tools are employed to ensure methodological rigour and transparency in guideline development. Such reporting instruments include the AGREE II and RIGHT, with the former being used for guideline development and appraisal, as well as reporting.

    Conclusion: This guide will help guideline developers/expert panels enhance their methodology, and patients/clinicians/policymakers interpret guideline recommendations and put them in context. This document may be a useful methodological summary for health guideline development by other societies and organisations.

  • 9. Arnelöv, Conny
    et al.
    Furebring, Mia
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Medical Sciences, Infectious Diseases.
    Wanhainen, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Aortagraftinfektion – ett komplicerat kärlkirurgiskt tillstånd2013In: Svensk Kirurgi, ISSN 0346-847X, Vol. 71, no 2, p. 84-88Article in journal (Refereed)
    Abstract [sv]

    Infektion runt ett aortagraft är en fruktad komplikation och utgör både en kirurgisk och antibakteriell utmaning där erfarenhet och multidisciplinär kompetens krävs. Åtgärder kan behövas akut vid graftenterisk blödning, men i andra fall med enbart infektion finns det tid för en noggrann utredning och diskussion angående kirurgisk strategi. 

  • 10.
    Arzola, Luis H.
    et al.
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Asciutto, Giuseppe
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Shehab, Maysam
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Wanhainen, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery. Umeå Univ, Dept Surg & Perioperat Sci, Surg, Umeå, Sweden..
    Mani, Kevin
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Outcome of a dedicated complex aortic surgery fellowship program2024In: Frontiers in Surgery, E-ISSN 2296-875X, Vol. 11, article id 1404641Article in journal (Refereed)
    Abstract [en]

    Introduction: Advancements in endovascular therapy, especially in complex aortic procedures, underscore the need for additional post-certification training. Dedicated post-residency vascular fellowship programs offer exposure to diverse cases, research opportunities, and professional networking. The study aims to describe and present outcomes from the complex aortic fellowship program at the Vascular Surgery Department of the Uppsala University Hospital.

    Methods: Nine former fellows who completed the aortic fellowship program at the Uppsala University Hospital from 2018 to 2023 were invited to take part in an anonymous 29-question survey through email. Demographic data, information about the existence of local aortic programs as well as on the types of aortic procedures performed were gained. The overall experience and impact of the fellowship were assessed using multiple interval scale questions, with a rating scale (1 excellent to 5 very poor). Finally, we provided the option to the participants to share additional feedback.

    Results: Median age of participants was 34 years (IQR, 30.5-36), with 44.4% being women (4/9). There was a significant variation in the number of publications produced during the fellowship, with an overall mean of 4 papers (IQR, 2-10). Regarding the long-term impact of the fellowship, 5/9 (55.6%) of the fellows have contributed to the implementation of a complex aortic program after finishing the fellowship, providing a broad range of complex aortic procedures. All fellows (9/9, 100%) stated that the quality of the fellowship was excellent. The clinical experience 7/9 (77.8%), the academic environment 7/9 (77.8%) and the research opportunities 7/9 (77.8%) together with the mentorship 9/9 (100%) and the work environment 8/9 (88.9%), were considered of most value among the fellows. In general, the survey participants agreed that the fellowship atmosphere was suitable for learning, 9/9 (100%), and that it had a positive impact on their current practice, 7/9 (77.8%). Currently, 5/9 (55.5%) of the fellows hold a position including academic involvement.

    Conclusions: There is a universal need for additional post-certification training. The current study showed that a balanced clinical and scientific exposure to complex aortic diseases is broadly welcomed among young vascular surgeons. The extension of the fellowship to cover other disciplines dealing with complex aortic procedures can be of value.

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  • 11.
    Arzola, Luis H.
    et al.
    Department of Surgical Sciences, Section of Vascular Surgery, Uppsala University, Uppsala, Sweden.
    Asciutto, Giuseppe
    Department of Surgical Sciences, Section of Vascular Surgery, Uppsala University, Uppsala, Sweden.
    Shehab, Maysam
    Department of Surgical Sciences, Section of Vascular Surgery, Uppsala University, Uppsala, Sweden.
    Wanhainen, Anders
    Umeå University, Faculty of Medicine, Department of Surgical and Perioperative Sciences, Surgery. Department of Surgical Sciences, Section of Vascular Surgery, Uppsala University, Uppsala, Sweden.
    Mani, Kevin
    Department of Surgical Sciences, Section of Vascular Surgery, Uppsala University, Uppsala, Sweden.
    Outcome of a dedicated complex aortic surgery fellowship program2024In: Frontiers in Surgery, E-ISSN 2296-875X, Vol. 11, article id 1404641Article in journal (Refereed)
    Abstract [en]

    Introduction: Advancements in endovascular therapy, especially in complex aortic procedures, underscore the need for additional post-certification training. Dedicated post-residency vascular fellowship programs offer exposure to diverse cases, research opportunities, and professional networking. The study aims to describe and present outcomes from the complex aortic fellowship program at the Vascular Surgery Department of the Uppsala University Hospital.

    Methods: Nine former fellows who completed the aortic fellowship program at the Uppsala University Hospital from 2018 to 2023 were invited to take part in an anonymous 29-question survey through email. Demographic data, information about the existence of local aortic programs as well as on the types of aortic procedures performed were gained. The overall experience and impact of the fellowship were assessed using multiple interval scale questions, with a rating scale (1 excellent to 5 very poor). Finally, we provided the option to the participants to share additional feedback.

    Results: Median age of participants was 34 years (IQR, 30.5-36), with 44.4% being women (4/9). There was a significant variation in the number of publications produced during the fellowship, with an overall mean of 4 papers (IQR, 2-10). Regarding the long-term impact of the fellowship, 5/9 (55.6%) of the fellows have contributed to the implementation of a complex aortic program after finishing the fellowship, providing a broad range of complex aortic procedures. All fellows (9/9, 100%) stated that the quality of the fellowship was excellent. The clinical experience 7/9 (77.8%), the academic environment 7/9 (77.8%) and the research opportunities 7/9 (77.8%) together with the mentorship 9/9 (100%) and the work environment 8/9 (88.9%), were considered of most value among the fellows. In general, the survey participants agreed that the fellowship atmosphere was suitable for learning, 9/9 (100%), and that it had a positive impact on their current practice, 7/9 (77.8%). Currently, 5/9 (55.5%) of the fellows hold a position including academic involvement.

    Conclusions: There is a universal need for additional post-certification training. The current study showed that a balanced clinical and scientific exposure to complex aortic diseases is broadly welcomed among young vascular surgeons. The extension of the fellowship to cover other disciplines dealing with complex aortic procedures can be of value.

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  • 12.
    Arzola, Luis H.
    et al.
    Department of Surgery, Section of Vascular Surgery and Endovascular Therapy, National Institute of Medical Sciences and Nutrition Salvador Zubirán, Mexico City, Mexico.
    Mani, Kevin
    Department of Surgical Sciences, Section of Vascular Surgery, Uppsala University, Uppsala, Sweden.
    Zuccon, Gianmarco
    Department of Surgical Sciences, Section of Vascular Surgery, Uppsala University, Uppsala, Sweden.
    Ekberg, Tomas
    Department of Otorhinolaryngology-Head and Neck Surgery, Uppsala University Hospital, Uppsala, Sweden.
    Wanhainen, Anders
    Umeå University, Faculty of Medicine, Department of Surgical and Perioperative Sciences, Surgery. Department of Surgical Sciences, Section of Vascular Surgery, Uppsala University, Uppsala, Sweden.
    Viabahn-assisted sutureless anastomosis (VASA) repair of a complex internal carotid artery aneurysm2023In: Journal of Vascular Surgery Cases and Innovative Techniques, E-ISSN 2468-4287, Vol. 9, no 2, article id 101161Article in journal (Refereed)
    Abstract [en]

    Extracranial carotid artery aneurysms (CAAs) are extremely rare and often require surgical intervention to avoid complications such as local compression symptoms and thrombo-embolization. We present the case of a 63-year-old man with a history of hypertension, meningioma, and an incidental finding of a right saccular internal carotid artery aneurysm at the base of the skull. He underwent open surgical repair; nonetheless, end-to-end anastomosis was not feasible. As bailout, the internal carotid artery was successfully reconstructed with a novel Viabahn-assisted sutureless anastomosis technique (GORE, Viabahn). Postoperative clinical assessment revealed no complications, postoperative computed tomography angiography revealed a patent reconstruction, and the patient was discharged home uneventfully with 1-year clinical and computed tomography angiography follow-up without remarks. Hybrid procedure is a viable option for technically challenging carotid anastomoses near the skull base.

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  • 13.
    Arzola, Luis H.
    et al.
    Natl Inst Med Sci & Nutr Salvador Zubiran, Dept Surg, Sect Vasc Surg & Endovasc Therapy, Mexico City, Mexico..
    Mani, Kevin
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Zuccon, Gianmarco
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Ekberg, Tomas
    Uppsala Univ Hosp, Dept Otorhinolaryngol Head & Neck Surg, Uppsala, Sweden..
    Wanhainen, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery. Umeå Univ, Dept Surg & Perioperat Sci, Surg, Umeå, Sweden..
    Viabahn-assisted sutureless anastomosis (VASA) repair of a complex internal carotid artery aneurysm2023In: Journal of Vascular Surgery Cases and Innovative Techniques, E-ISSN 2468-4287, Vol. 9, no 2, article id 101161Article in journal (Refereed)
    Abstract [en]

    Extracranial carotid artery aneurysms (CAAs) are extremely rare and often require surgical intervention to avoid complications such as local compression symptoms and thrombo-embolization. We present the case of a 63-year-old man with a history of hypertension, meningioma, and an incidental finding of a right saccular internal carotid artery aneurysm at the base of the skull. He underwent open surgical repair; nonetheless, end-to-end anastomosis was not feasible. As bailout, the internal carotid artery was successfully reconstructed with a novel Viabahn-assisted sutureless anastomosis technique (GORE, Viabahn). Postoperative clinical assessment revealed no complications, postoperative computed tomography angiography revealed a patent reconstruction, and the patient was discharged home uneventfully with 1-year clinical and computed tomography angiography follow-up without remarks. Hybrid procedure is a viable option for technically challenging carotid anastomoses near the skull base.

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  • 14.
    Asciutto, Giuseppe
    et al.
    Division of Vascular Surgery, Department of Surgical Sciences, Uppsala University, Uppsala, Sweden.
    Ibrahim, Abdulhakim
    Department of Vascular and Endovascular Surgery, University Hospital Münster, Münster, Germany.
    Leone, Nicola
    Department of Vascular Surgery, Ospedale Civile di Baggiovara, Azienda Ospedaliero-Universitaria di Modena, Università di Modena e Reggio Emilia, Modena, Italy.
    Gennai, Stefano
    Department of Vascular Surgery, Ospedale Civile di Baggiovara, Azienda Ospedaliero-Universitaria di Modena, Università di Modena e Reggio Emilia, Modena, Italy.
    Piazza, Michele
    Vascular and Endovascular Surgery Division, Department of Cardiac, Thoracic, Vascular Sciences and Public Health, Padua University, Padua, Italy.
    Antonello, Michele
    Vascular and Endovascular Surgery Division, Department of Cardiac, Thoracic, Vascular Sciences and Public Health, Padua University, Padua, Italy.
    Wanhainen, Anders
    Umeå University, Faculty of Medicine, Department of Surgical and Perioperative Sciences, Surgery. Division of Vascular Surgery, Department of Surgical Sciences, Uppsala University, Uppsala, Sweden.
    Mani, Kevin
    Division of Vascular Surgery, Department of Surgical Sciences, Uppsala University, Uppsala, Sweden.
    Lindström, David
    Division of Vascular Surgery, Department of Surgical Sciences, Uppsala University, Uppsala, Sweden.
    Struk, Lisa
    Department of Vascular and Endovascular Surgery, University Hospital Münster, Münster, Germany.
    Oberhuber, Alexander
    Department of Vascular and Endovascular Surgery, University Hospital Münster, Münster, Germany.
    Intravascular ultrasound in the detection of bridging stent graft instability during fenestrated and branched endovascular aneurysm repair procedures: a multicentre study on 274 target vessels2024In: European Journal of Vascular and Endovascular Surgery, ISSN 1078-5884, E-ISSN 1532-2165, Vol. 67, no 1, p. 99-104Article in journal (Refereed)
    Abstract [en]

    Objective: The use of intravascular ultrasound (IVUS) reduces contrast medium use and radiation exposure during conventional endovascular aneurysm repair (EVAR). The aim of this study was to evaluate the safety and efficacy of IVUS in detecting bridging stent graft (bSG) instability during fenestrated and branched EVAR (F/B-EVAR).

    Methods: This was a prospective observational multicentre study. The following outcomes were evaluated: (1) technical success of the IVUS in each bSG, (2) IVUS findings compared with intra-operative angiography, (3) incidence of post-operative computed tomography angiography (CTA) findings not detected with IVUS, and (4) absence of IVUS related adverse events. Target visceral vessel (TVV) instability was defined as any branch or fenestration issues requiring an additional manoeuvre or re-intervention. Any IVUS assessment that detected stenosis, kinking, or any geometric TVV issue was considered to be branch instability. All procedures were performed in ad hoc hybrid rooms.

    Results: Eighty patients (69% males; median age 72 years; interquartile range 59, 77 years) from four aortic centres treated with F/B-EVAR between January 2019 and September 2021 were included: 70 BEVAR (21 off the shelf; 49 custom made), eight FEVAR (custom made), and two F/B-EVAR (custom made), for a total of 300 potential TVVs. Two TVVs (0.7%) were left unstented and excluded from the analysis. The TVVs could not be accessed with the IVUS catheter in seven cases (2.3%). Furthermore, 17 (5.7%) TVVs could not be examined due to a malfunction of the IVUS catheter. The technical success of the IVUS assessment was 91.9% (274/298), with no IVUS related adverse events. Seven TVVs (2.5%) showed signs of bSG instability by means of IVUS, leading to immediate revisions. The first post-operative CTA at least 30 days after the index procedure was available in 268 of the 274 TVVs originally assessed by IVUS. In seven of the 268 TVVs (2.6%) a re-intervention became necessary due to bSG instability.

    Conclusion: This study suggests that IVUS is a safe and potentially valuable adjunctive imaging technology for intra-operative detection of TVV instability. Further long term investigations on larger cohorts are required to validate these promising results and to compare IVUS with alternative technologies in terms of efficiency, radiation exposure, procedure time, and costs.

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  • 15.
    Asciutto, Giuseppe
    et al.
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Ibrahim, Abdulhakim
    Leone, Nicola
    Gennai, Stefano
    Piazza, Michele
    Antonello, Michele
    Wanhainen, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery. Department of Surgical and Peri-operative Sciences, Surgery, Umeå University, Umeå, Sweden..
    Mani, Kevin
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Lindström, David
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Struk, Lisa
    Oberhuber, Alexander
    Intravascular Ultrasound in the Detection of Bridging Stent Graft Instability During Fenestrated and Branched Endovascular Aneurysm Repair Procedures: A Multicentre Study on 274 Target Vessels2024In: European Journal of Vascular and Endovascular Surgery, ISSN 1078-5884, E-ISSN 1532-2165, Vol. 67, no 1, p. 99-104, article id S1078-5884(23)00740-2Article in journal (Refereed)
    Abstract [en]

    OBJECTIVE: The use of intravascular ultrasound (IVUS) reduces contrast medium use and radiation exposure during conventional endovascular aneurysm repair (EVAR). The aim of this study was to evaluate the safety and efficacy of IVUS in detecting bridging stent graft (bSG) instability during fenestrated and branched EVAR (F/B-EVAR).

    METHODS: This was a prospective observational multicentre study. The following outcomes were evaluated: (1) technical success of the IVUS in each bSG, (2) IVUS findings compared with intra-operative angiography, (3) incidence of post-operative computed tomography angiography (CTA) findings not detected with IVUS, and (4) absence of IVUS related adverse events. Target visceral vessel (TVV) instability was defined as any branch or fenestration issues requiring an additional manoeuvre or re-intervention. Any IVUS assessment that detected stenosis, kinking, or any geometric TVV issue was considered to be branch instability. All procedures were performed in ad hoc hybrid rooms.

    RESULTS: Eighty patients (69% males; median age 72 years; interquartile range 59, 77 years) from four aortic centres treated with F/B-EVAR between January 2019 and September 2021 were included: 70 BEVAR (21 off the shelf; 49 custom made), eight FEVAR (custom made), and two F/B-EVAR (custom made), for a total of 300 potential TVVs. Two TVVs (0.7%) were left unstented and excluded from the analysis. The TVVs could not be accessed with the IVUS catheter in seven cases (2.3%). Furthermore, 17 (5.7%) TVVs could not be examined due to a malfunction of the IVUS catheter. The technical success of the IVUS assessment was 91.9% (274/298), with no IVUS related adverse events. Seven TVVs (2.5%) showed signs of bSG instability by means of IVUS, leading to immediate revisions. The first post-operative CTA at least 30 days after the index procedure was available in 268 of the 274 TVVs originally assessed by IVUS. In seven of the 268 TVVs (2.6%) a re-intervention became necessary due to bSG instability.

    CONCLUSION: This study suggests that IVUS is a safe and potentially valuable adjunctive imaging technology for intra-operative detection of TVV instability. Further long term investigations on larger cohorts are required to validate these promising results and to compare IVUS with alternative technologies in terms of efficiency, radiation exposure, procedure time, and costs.

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  • 16.
    Baderkhan, Hassan
    et al.
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Gonçalves, Frederico M. Bastos
    Erasmus Univ, Dept Vasc Surg, Med Ctr, Rotterdam, Netherlands; Hosp Santa Marta, Dept Angiol & Vasc Surg, Ctr Hosp Lisboa Cent, Lisbon, Portugal.
    Oliveira, Nelson Gomes
    Erasmus Univ, Dept Vasc Surg, Med Ctr, Rotterdam, Netherlands; Hosp Divino Espirito Santo Ponta Delgada, Dept Angiol & Vasc Surg, Azores, Portugal.
    Verhagen, Hence J. M.
    Erasmus Univ, Dept Vasc Surg, Med Ctr, Rotterdam, Netherlands.
    Wanhainen, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Björck, Martin
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Mani, Kevin
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Challenging Anatomy Predicts Mortality and Complications After Endovascular Treatment of Ruptured Abdominal Aortic Aneurysm2016In: Journal of Endovascular Therapy, ISSN 1526-6028, E-ISSN 1545-1550, Vol. 23, no 6, p. 919-927Article in journal (Refereed)
    Abstract [en]

    PURPOSE: To analyze the effects of aortic anatomy and endovascular aneurysm repair (EVAR) inside and outside the instructions for use (IFU) on outcomes in patients treated for ruptured abdominal aortic aneurysms (rAAA).

    METHODS: All 112 patients (mean age 73 years; 102 men) treated with standard EVAR for rAAA between 2000 and 2012 in 3 European centers were included in the retrospective analysis. Patients were grouped based on aortic anatomy and whether EVAR was performed inside or outside the IFU. Data on complications, secondary interventions, and mortality were extracted from the patient records. Cox regression analysis was performed to assess predictors of mortality and complications; results are presented as the hazard ratio (HR) with 95% confidence interval (CI). Survival was analyzed using the Kaplan-Meier method.

    RESULTS: Of the 112 patients examined, 61 (54%) were treated inside the IFU, 43 (38%) outside the IFU, and 8 patients lacked adequate preoperative computed tomography scans for determination. Median follow-up of those surviving 30 days was 2.5 years. Mortality at 30 days was 15% (95% CI 6% to 24%) inside the IFU vs 30% (95% CI 16% to 45%) outside (p=0.087). Three-year mortality estimates were 33.8% (95% CI 20.0% to 47.5%) inside the IFU vs 56% (95% CI 39.7% to 72.2%) outside (p=0.016). At 5 years, mortality was 48% (95% CI 30% to 66%) inside the IFU vs 74% (95% CI 54% to 93%) outside (p=0.015). Graft-related complications occurred in 6% (95% CI 0% to 13%) inside the IFU and 30% (95% CI 14% to 42%) outside (p=0.015). The rate of graft-related secondary interventions was 14% (95% CI 4% to 22%) inside the IFU vs 35% (95% CI 14% to 42%) outside (p=0.072). In the multivariate analysis, neck length <15 mm (HR 8.1, 95% CI 3.0 to 21.9, p<0.001) and angulation >60° (HR 3.1, 95% CI 1.0 to 9.3, p=0.045) were independent predictors of late graft-related complications. Aneurysm neck diameter >29 mm (HR 2.5, 95% CI 1.1 to 5.9, p=0.035) was an independent predictor of overall mortality.

    CONCLUSION: Long-term mortality and complications after rEVAR are associated with aneurysm anatomy. The role of adjunct endovascular techniques and the outcome of open repair in cases with challenging anatomy warrant further study.

  • 17.
    Baderkhan, Hassan
    et al.
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Haller, O.
    Department of Radiology, Gävle Hospital, Gävle, Sweden.
    Wanhainen, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Björck, Martin
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Mani, Kevin
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Follow-up after endovascular aortic aneurysm repair can be stratified based on first postoperative imaging2018In: British Journal of Surgery, ISSN 0007-1323, E-ISSN 1365-2168, Vol. 05, no 6, p. 709-718Article in journal (Refereed)
    Abstract [en]

    Background

    Lifelong postoperative surveillance is recommended following endovascular aneurysm repair (EVAR). Although the purpose is to prevent and/or identify complications early, it also results in increased cost and workload. This study was designed to examine whether it may be possible to identify patients at low risk of complications based on their first postoperative CT angiogram (CTA).

    Methods

    All patients undergoing EVAR in two Swedish centres between 2001 and 2012 were identified retrospectively and categorized based on the first postoperative CTA as at low risk (proximal and distal sealing zone at least 10 mm and no endoleak) or high risk (sealing zone less than 10 mm and/or presence of any endoleak) of complications.

    Results

    Some 326 patients (273 men) with a CTA performed less than 1 year after EVAR were included (low risk 212, 65·0 per cent; high risk 114, 35·0 per cent). There was no difference between the groups in terms of sex, age, co‐morbidities, abdominal aortic aneurysm (AAA) diameter, preoperative AAA neck anatomy, stent‐graft type or duration of follow‐up (mean(s.d.) 4·8(3·2) years). Five‐year freedom from AAA‐related adverse events was 97·1 and 47·7 per cent in the low‐ and high‐risk groups respectively (P < 0·001). The corresponding freedom from AAA‐related reintervention was 96·2 and 54·1 per cent (P < 0·001). The method had a sensitivity of 88·3 per cent, specificity of 77·0 per cent and negative predictive value of 96·6 per cent to detect AAA‐related adverse events. The number of surveillance imaging per AAA‐related adverse event was 168 versus 11 for the low‐risk versus high‐risk group.

    Conclusion

    Two‐thirds of patients undergoing EVAR have an adequate seal and no endoleak on the first postoperative CTA, and a very low risk of AAA‐related events up to 5 years. Less vigilant follow‐up after EVAR may be considered for these patients.

  • 18.
    Baderkhan, Hassan
    et al.
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Wanhainen, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Haller, Olov
    Gävle Cent Hosp, Dept Radiol, Gävle, Sweden..
    Björck, Martin
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Mani, Kevin
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Detection of Late Complications After Endovascular Abdominal Aortic Aneurysm Repair and Implications for Follow up Based on Retrospective Assessment of a Two Centre Cohort2020In: European Journal of Vascular and Endovascular Surgery, ISSN 1078-5884, E-ISSN 1532-2165, Vol. 60, no 2, p. 171-179Article in journal (Refereed)
    Abstract [en]

    Objective. Endovascular aortic aneurysm repair (EVAR) is associated with the risk of late complications and mandates follow up. This retrospective study assessed post-EVAR complications in a two centre cohort. The study evaluated the rate of complications presenting with symptoms vs. those detected by imaging follow up. Additionally, the agreement between DUS and CTA in detecting complications was assessed in patients with both. Methods: All EVAR patients from 1998 to 2012 in two centres were included. Complications were classified based on whether they were symptomatic or detected by imaging, as well as based on imaging detection modality (DUS or CTA). For patients who had undergone DUS and CTA within three months of each other, the kappa coefficient of agreement was assessed. Results: Four hundred and fifty-four patients treated by EVAR were identified. The median follow up time was 5.2 (IQR 2.8-7.6) years. One hundred and eighteen patients (26%) developed 176 complications. One hundred and six (60.2%) of the complications were asymptomatic, and 70 (39.8%) were symptomatic. Two hundred and fifty-three patients had imaging with both modalities within three months of each other; the kappa coefficient for agreement between CTA and DUS for detecting clinically significant complications was 0.91. Regarding CTA as the standard modality, DUS had a sensitivity of 88.8% (95% CI 77.3-95.8%) and a specificity of 99.4% (95% CI 97.1-99.9%). Three of the complications missed by DUS were related to loss of proximal and distal seal, all occurring in patients with short sealing length on first post-operative CT scan. Conclusion: Approximately a quarter of the patients developed complications, the majority of which were asymptomatic, underlining the importance of adequate surveillance. There was good agreement between CTA and DUS in detecting complications. Clinically significant complications related to inadequate seal were missed by DUS, suggesting that CTA still plays an important role in EVAR surveillance.

  • 19.
    Baderkhan, Hassan
    et al.
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Wanhainen, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Stenborg, Anna
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Medical Sciences.
    Stattin, Evalena
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Immunology, Genetics and Pathology, Medicinsk genetik och genomik. Uppsala University, Science for Life Laboratory, SciLifeLab.
    Björck, Martin
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Celiprolol Treatment in Patients with Vascular Ehlers-Danlos Synurome2021In: European Journal of Vascular and Endovascular Surgery, ISSN 1078-5884, E-ISSN 1532-2165, Vol. 61, no 2, p. 326-331Article in journal (Refereed)
    Abstract [en]

    Objecti_ Vascular Ehlers-Danlos syndrome (vEDS) is a rare monogenetic disease caused by pathogenic variants in procollagen 3A1. Arterial rupture is the most serious clinical manifestation. A randomised controlled trial, the Beta-Blockers in Ehlers-Danlos Syndrome Treatment (BBEST) trial, reported a significant protective effect of the beta blocker celiprolol. The aim was to study the outcome of celiprolol treatment in a cohort of Swedish patients with vEDS. Methods: Uppsala is a national referral centre for patients with vEDS. They are assessed by vascular surgeons, angiologists, and clinical geneticists. Family history, previous and future clinical events, medication, and side effects are registered. Celiprolol was administered twice daily and titrated up to a maximum dose of 400 mg daily. Logistic regression was used to analyse predictors of vascular events. Results: Forty patients with pathogenic sequence variants in COL3A1 were offered treatment with celiprolol in the period 2011-2019. The median follow up was 22 months (range 1-98 months); total follow up was 106 patient years. In two patients, uptitration of the dose is ongoing. Of the remaining 38, 26 (65%) patients reached the target dose of 400 mg daily. Dose uptitration was unsuccessful in six patients because of side effects; one died before reaching the maximum dose, and five terminated the treatment. Five major vascular events occurred; four were fatal (ruptured ascending aorta; aortic rupture after type B dissection; ruptured cerebral aneurysm; and ruptured pulmonary artery). One bled from a branch of the internal iliac artery, which was successfully coiled endovascularly. The annual risk of a major vascular event was 4.7% (n = 5/106), similar to the treatment arm of the BBEST trial (5%) and lower than in the control arm of the same trial (12%). No significant predictor of vascular events was identified. Conclusion: Treatment with celiprolol is tolerated in most patients with vEDS. Despite fatal vascular events, these observations suggest that celiprolol may have a protective effect in vEDS.

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  • 20.
    Balboa Ramilo, Amanda
    et al.
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Medical Cell Biology.
    Becirovic Agic, Mediha
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Medical Cell Biology.
    Petri, Marcelo Heron
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Medical Cell Biology.
    Mani, Kevin
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Wanhainen, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery. Umeå Univ, Dept Surg & Perioperat Sci, Surg, Umeå, Sweden..
    Wågsäter, Dick
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Medical Cell Biology.
    The tyrosine kinase inhibitor Bosutinib does not inhibit angiotensin II-induced abdominal aortic aneurysm: Validation of the importance of PDGFR and c-Kit tyrosine kinases by Imatinib2022In: Atherosclerosis, ISSN 0021-9150, E-ISSN 1879-1484, Vol. 340, p. 68-69Article in journal (Refereed)
  • 21.
    Balboa Ramilo, Amanda
    et al.
    Department of Medical Cell Biology, Uppsala University, Uppsala, Sweden.
    Becirovic-Agic, Mediha
    Department of Medical Cell Biology, Uppsala University, Uppsala, Sweden.
    Petri, Marcelo Heron
    Department of Medical Cell Biology, Uppsala University, Uppsala, Sweden.
    Mani, Kevin
    Department of Surgical Sciences, Section of Vascular Surgery, Uppsala University, Uppsala, Sweden.
    Wanhainen, Anders
    Umeå University, Faculty of Medicine, Department of Surgical and Perioperative Sciences, Surgery. Department of Surgical Sciences, Section of Vascular Surgery, Uppsala University, Uppsala, Sweden.
    Wågsäter, Dick
    Department of Medical Cell Biology, Uppsala University, Uppsala, Sweden.
    The tyrosine kinase inhibitor Bosutinib does not inhibit angiotensin II-induced abdominal aortic aneurysm: Validation of the importance of PDGFR and c-Kit tyrosine kinases by Imatinib2022In: Atherosclerosis, ISSN 0021-9150, E-ISSN 1879-1484, Vol. 340, p. 68-69Article in journal (Other academic)
  • 22.
    Bastos Gonçalves, Frederico
    et al.
    Hospital de Santa Marta, Unidade Local de Saúde São José, Centro Clínico Académico de Lisboa, Lisbon, Portugal; NOVA Medical School | Faculdade de Ciências Médicas, NMS|FCM, Universidade Nova de Lisboa, Lisbon, Portugal; Hospital CUF Tejo, Lisbon, Portugal.
    Wanhainen, Anders
    Umeå University, Faculty of Medicine, Department of Surgical and Perioperative Sciences, Surgery. Department of Surgical Sciences, Vascular Surgery, Uppsala University, Uppsala, Sweden.
    The one size fits all EVAR follow up has proven unsuccessful and is a thing of the past2024In: European Journal of Vascular and Endovascular Surgery, ISSN 1078-5884, E-ISSN 1532-2165, Vol. 67, no 5, p. 703-704Article in journal (Other academic)
  • 23.
    Bath, Jonathan
    et al.
    Univ Missouri, Div Vasc Surg, Columbia, MO 65212 USA..
    D'Oria, Mario
    Univ Hosp Trieste ASUGI, Cardiovasc Dept, Div Vasc & Endovasc Surg, Trieste, Italy..
    Rogers, Richard T.
    Mayo Clin, Dept Surg, Div Vasc & Endovasc Surg, Rochester, NY USA..
    Colglazier, Jill J.
    Mayo Clin, Dept Surg, Div Vasc & Endovasc Surg, Rochester, NY USA..
    Braet, Drew J.
    Univ Michigan, Dept Surg, Div Vasc Surg, Ann Arbor, MI USA..
    Coleman, Dawn M.
    Univ Michigan, Dept Surg, Div Vasc Surg, Ann Arbor, MI USA..
    Scali, Salvatore T.
    Univ Florida, Div Vasc & Endovasc Therapy, Coll Med, Gainesville, FL USA..
    Back, Martin R.
    Univ Florida, Div Vasc & Endovasc Therapy, Coll Med, Gainesville, FL USA..
    Magee, Gregory A.
    Univ Southern Calif, Dept Surg, Div Vasc & Endovasc Therapy, Los Angeles, CA USA..
    Plotkin, Anastasia
    Univ Southern Calif, Dept Surg, Div Vasc & Endovasc Therapy, Los Angeles, CA USA..
    Dueppers, Philip
    Univ Hosp Zurich, Dept Vasc Surg, Zurich, Switzerland.;Univ Messina, Dept Med Sci & Morphofunct Imaging, Div Vasc Surg, Messina, Italy..
    Zimmermann, Alexander
    Univ Hosp Zurich, Dept Vasc Surg, Zurich, Switzerland..
    Affi, Rana O.
    UTHealth, Cardiothorac & Vasc Surg, McGovern Med Sch, Houston, TX USA..
    Khan, Sophia
    UTHealth, Cardiothorac & Vasc Surg, McGovern Med Sch, Houston, TX USA..
    Zarkowsky, Devin
    Univ Colorado, Dept Surg, Div Vasc Surg, Sch Med, Aurora, CO USA..
    Dyba, Gregory
    Univ Colorado, Dept Surg, Div Vasc Surg, Sch Med, Aurora, CO USA..
    Soult, Michael C.
    Loyola Univ Chicago, Stritch Sch Med, Dept Surg, Div Vasc Surg & Endovasc Therapy, Maywood, IL USA..
    Mani, Kevin
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Wanhainen, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Setacci, Carlo
    Univ Siena, Dept Med Surg & Neurosci, Div Vasc & Endovasc Surg, Siena, Italy..
    Lenti, Massimo
    Univ Siena, Dept Med Surg & Neurosci, Div Vasc & Endovasc Surg, Siena, Italy..
    Kabbani, Loay S.
    Henry Ford Hosp, Dept Surg, Div Vasc Surg, Detroit, MI USA..
    Weaver, Mitchelle R.
    Henry Ford Hosp, Dept Surg, Div Vasc Surg, Detroit, MI USA..
    Bissacco, Daniele
    IRCCS Ca Granda Osped Maggiore Policlin, Dept Vasc Surg, Milan, Italy..
    Trimarchi, Santi
    IRCCS Ca Granda Osped Maggiore Policlin, Dept Vasc Surg, Milan, Italy..
    Stoecker, Jordan B.
    Hosp Univ Penn, Div Vasc Surg & Endovasc Therapy, Dept Surg, Philadelphia, PA USA..
    Wang, Grace J.
    Hosp Univ Penn, Div Vasc Surg & Endovasc Therapy, Dept Surg, Philadelphia, PA USA..
    Szeberin, Zoltan
    Semmelweis Univ, Dept Vasc & Endovasc Surg, Budapest, Hungary..
    Pomozi, Eniko
    Semmelweis Univ, Dept Vasc & Endovasc Surg, Budapest, Hungary..
    Moffatt, Clare
    Univ Calif Los Angeles, Div Vasc & Endovasc Surg, Dept Surg, David Geffen Sch Med, Los Angeles, CA USA..
    Gelabert, Hugh A.
    Univ Calif Los Angeles, Div Vasc & Endovasc Surg, Dept Surg, David Geffen Sch Med, Los Angeles, CA USA..
    Tish, Shahed
    Univ Missouri, Div Vasc Surg, Columbia, MO 65212 USA..
    Hoel, Andrew W.
    Northwestern Univ, Dept Surg, Div Vasc Surg, Feinberg Sch Med, Chicago, IL USA..
    Cortolillo, Nicholas S.
    Northwestern Univ, Dept Surg, Div Vasc Surg, Feinberg Sch Med, Chicago, IL USA..
    Spangler, Emily L.
    Univ Alabama Birmingham, Dept Surg, Div Vasc Surg & Endovasc Therapy, Birmingham, AL USA..
    Passman, Marc A.
    Univ Alabama Birmingham, Dept Surg, Div Vasc Surg & Endovasc Therapy, Birmingham, AL USA..
    De Caridi, Giovanni
    Univ Messina, Dept Med Sci & Morphofunct Imaging, Div Vasc Surg, Messina, Italy..
    Benedetto, Filippo
    Zhou, Wei
    Univ Arizona, Dept Surg, Div Vasc Surg, Tucson, AZ USA..
    Abuhakmeh, Yousef
    Univ Arizona, Dept Surg, Div Vasc Surg, Tucson, AZ USA..
    Newton, Daniel H.
    Virginia Commonwealth Univ, Dept Surg, Div Vasc Surg, Sch Med, Richmond, VA USA..
    Liu, Christopher M.
    Virginia Commonwealth Univ, Dept Surg, Div Vasc Surg, Sch Med, Richmond, VA USA..
    Tinelli, Giovanni
    Univ Cattolica Sacro Cuore, Fdn Policlin Univ A Gemelli IRCCS, Dept Cardiovasc Sci, Unit Vasc Surg, Rome, Italy..
    Tshomba, Yamume
    Univ Cattolica Sacro Cuore, Fdn Policlin Univ A Gemelli IRCCS, Dept Cardiovasc Sci, Unit Vasc Surg, Rome, Italy..
    Katoh, Airi
    Univ Calif San Francisco Fresno, Dept Surg, Fresno, CA USA..
    Siada, Sammy S.
    Univ Calif San Francisco Fresno, Dept Surg, Fresno, CA USA..
    Khashram, Manar
    Univ Auckland, Dept Surg, Waikato, New Zealand..
    Gormley, Sinead
    Univ Auckland, Dept Surg, Waikato, New Zealand..
    Mullins, John R.
    CoxHealth, Dept Surg, Div Vasc Surg, Springfield, MO USA..
    Schmittling, Zachary C.
    CoxHealth, Dept Surg, Div Vasc Surg, Springfield, MO USA..
    Maldonado, Thomas S.
    New York Univ Langone Hlth, Dept Surg, Div Vasc Surg, New York, NY USA..
    Politano, Amani D.
    Oregon Hlth & Sci Univ, Dept Surg, Div Vasc Surg, Portland, OR USA..
    Rynio, Pawel
    Pomeranian Med Univ, Dept Vasc Surg, Szczecin, Poland..
    Kazimierczak, Arkadiusz
    Pomeranian Med Univ, Dept Vasc Surg, Szczecin, Poland..
    Gombert, Alexander
    Univ Hosp RWTH Aachen, European Vasc Ctr Aachen Maastricht, Dept Vasc Surg, Aachen, Germany..
    Jalaie, Houman
    Univ Hosp RWTH Aachen, European Vasc Ctr Aachen Maastricht, Dept Vasc Surg, Aachen, Germany..
    Spath, Paolo
    Univ Bologna, Dept Vasc Surg, DIMES, Bologna, Italy..
    Gallitto, Enrico
    Univ Bologna, Dept Vasc Surg, DIMES, Bologna, Italy..
    Czerny, Martin
    Albert Ludwigs Univ Freiburg, Univ Heart Ctr Freiburg Bad Krozingen, Univ Clin Freiburg, Clin Cardiovasc Surg, Freiburg, Germany..
    Berger, Tim
    Albert Ludwigs Univ Freiburg, Univ Heart Ctr Freiburg Bad Krozingen, Univ Clin Freiburg, Clin Cardiovasc Surg, Freiburg, Germany..
    Davies, Mark G.
    UT Hlth San Antonio, Long Sch Med, Div Vasc & Endovasc Surg, San Antonio, TX USA..
    Stilo, Francesco
    Montelione, Nunzio
    Univ Campus Biomed Rome, Dept Med & Surg, Operat Res Unit Vasc Surg, Rome, Italy..
    Mezzetto, Luca
    Integrated Univ Hosp Verona, Div Vasc Surg, Verona, Italy..
    Veraldi, Gian Franco
    Integrated Univ Hosp Verona, Div Vasc Surg, Verona, Italy..
    Lepidi, Sandro
    Univ Hosp Trieste ASUGI, Cardiovasc Dept, Div Vasc & Endovasc Surg, Trieste, Italy..
    Lawrence, Peter
    Univ Calif Los Angeles, Div Vasc & Endovasc Surg, Dept Surg, David Geffen Sch Med, Los Angeles, CA USA..
    Woo, Karen
    Univ Calif Los Angeles, Div Vasc & Endovasc Surg, Dept Surg, David Geffen Sch Med, Los Angeles, CA USA..
    Contemporary outcomes after treatment of aberrant subclavian artery and Kommerell's diverticulum2023In: Journal of Vascular Surgery, ISSN 0741-5214, E-ISSN 1097-6809, Vol. 77, no 5, p. 1339-1348.e6Article in journal (Refereed)
    Abstract [en]

    Objective: Aberrant subclavian artery (ASA) and Kommerell's diverticulum (KD) are rare vascular anomalies that may be associated with lifestyle-limiting and life-threatening complications. The aim of this study is to report contemporary outcomes after invasive treatment of ASA/KD using a large international dataset.

    Methods: Patients who underwent treatment for ASA/KD (2000-2020) were identified through the Vascular Low Frequency Disease Consortium, a multi-institutional collaboration to investigate uncommon vascular disorders. We report the early and mid-term clinical outcomes including stroke and mortality, technical success, and other operative outcomes including reintervention rates, patency, and endoleak.

    Results: Overall, 285 patients were identified during the study period. The mean patient age was 57 years; 47% were female and 68% presented with symptoms. A right-sided arch was present in 23%. The mean KD diameter was 47.4 mm (range, 13.0-108.0 mm). The most common indication for treatment was symptoms (59%), followed by aneurysm size (38%). The most common symptom reported was dysphagia (44%). A ruptured KD was treated in 4.2% of cases, with a mean diameter of 43.9 mm (range, 18.0-100.0 mm). An open procedure was performed in 101 cases (36%); the most common approach was ASA ligation with subclavian transposition. An endovascular or hybrid approach was performed in 184 patients (64%); the most common approach was thoracic endograft and carotid-subclavian bypass. A staged operative strategy was employed more often than single setting repair (55% vs 45%). Compared with endovascular or hybrid approach, those in the open procedure group were more likely to be younger (49 years vs 61 years; P < .0001), female (64% vs 36%; P < .0001), and symptomatic (85% vs 59%; P < .0001). Complete or partial symptomatic relief at 1 year after intervention was 82.6%. There was no association between modality of treatment and symptom relief (open 87.2% vs endovascular or hybrid approach 78.9%; P = .13). After the intervention, 11 subclavian occlusions (4.5%) occurred; 3 were successfully thrombectomized resulting in a primary and secondary patency of 95% and 96%, respectively, at a median follow-up of 39 months. Among the 33 reinterventions (12%), the majority were performed for endoleak (36%), and more reinterventions occurred in the endovascular or hybrid approach than open procedure group (15% vs 6%; P = .02). The overall survival rate was 87.3% at a median follow-up of 41 months. The 30-day stroke and death rates were 4.2% and 4.9%, respectively. Urgent or emergent presentation was independently associated with increased risk of 30-day mortality (odds ratio [OR], 19.8; 95% confidence interval [CI], 3.3-116.6), overall mortality (OR, 3.6; 95% CI, 1.2-11.2) and intraoperative complications (OR, 8.3; 95% CI, 2.8-25.1). Females had a higher risk of reintervention (OR, 2.6; 95% CI, 1.0-6.5). At an aneurysm size of 44.4 mm, receiver operator characteristic curve analysis suggested that 60% of patients would have symptoms.

    Conclusions: Treatment of ASA/KD can be performed safely with low rates of mortality, stroke and reintervention and high rates of symptomatic relief, regardless of the repair strategy. Symptomatic and urgent operations were associated with worse outcomes in general, and female gender was associated with a higher likelihood of reintervention. Given the worse overall outcomes when symptomatic and the inherent risk of rupture, consideration of repair at 40 mm is reasonable in most patients. ASA/KD can be repaired in asymptomatic patients with excellent outcomes and young healthy patients may be considered better candidates for open approaches versus endovascular or hybrid modalities, given the lower likelihood of reintervention and lower early mortality rate.

  • 24.
    Bengts, Sophy
    et al.
    Linköping Univ, Dept Med & Hlth Sci, Div Drug Res, Linköping, Sweden..
    Shamoun, Levar
    Jönköping Cty, Dept Lab Med, Div Med Diagnost, Jönköping, Sweden.;Uppsala Univ, Dept Med Cell Biol, BOX 571, SE-75123 Uppsala, Sweden..
    Kunath, Anne
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Medical Cell Biology.
    Appelgren, Daniel
    Linköping Univ, Dept Med & Hlth Sci, Div Drug Res, Linköping, Sweden..
    Welander, Martin
    Linköping Univ, Dept Med & Hlth Sci, Div Cardiovasc Med, Linköping, Sweden..
    Björck, Martin
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Wanhainen, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Wågsäter, Dick
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Medical Cell Biology. Linköping Univ, Dept Med & Hlth Sci, Div Drug Res, Linköping, Sweden..
    Altered IL-32 Signaling in Abdominal Aortic Aneurysm2020In: Journal of Vascular Research, ISSN 1018-1172, E-ISSN 1423-0135, Vol. 57, no 4, p. 236-244Article in journal (Refereed)
    Abstract [en]

    Introduction and Objective:Interleukin (IL)-32 is a pro-inflammatory cytokine not previously studied in relation to abdominal aortic aneurysm (AAA). The aim of this study was to elucidate the expression and localization of IL-32 in AAA.Methods:Expression and localization of IL-32 in human aortic tissue was studied with immunohistochemical analysis and Western blot (AAA:n= 5; controls:n= 4). ELISA was used to measure IL-32 in human plasma samples (AAA:n= 140; controls:n= 37) and in media from cultured peripheral blood mononuclear cells (PBMCs) from 3 healthy donors. IL-32 mRNA in PBMCs, endothelial cells, aortic smooth muscle cells (SMCs), and aortic tissue samples of AAA (n= 16) and control aortas (n= 9) was measured with qPCR.Results:IL-32 was predominantly expressed in SMCs and T-cell-rich areas. Highest mRNA expression was observed in the intima/media layer of the AAA. A weaker protein expression was detected in non-aneurysmal aortas. Expression of IL-32 was confirmed in isolated T cells, macrophages, endothelial cells, and SMCs, where expression was also inducible by cytokines such as interferon-gamma. There was no difference in IL-32 expression in plasma between patients and controls.Conclusion:IL-32 signaling is altered locally in AAA and could potentially play an important role in aneurysm development. Further studies using animal models would be helpful to study its potential role in AAA disease.

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  • 25.
    Benson, Tyler W.
    et al.
    Univ Cincinnati, Dept Internal Med, Coll Med, Cincinnati, OH USA.;Univ Cincinnati, Div Cardiovasc Hlth & Dis, Coll Med, Cincinnati, OH USA..
    Conrad, Kelsey A.
    Univ Cincinnati, Dept Internal Med, Coll Med, Cincinnati, OH USA.;Univ Cincinnati, Div Cardiovasc Hlth & Dis, Coll Med, Cincinnati, OH USA.;Univ Cincinnati, Pathobiol & Mol Med Grad Program, Coll Med, Cincinnati, OH USA..
    Li, Xinmin S.
    Cleveland Clin, Dept Cardiovasc & Metab Sci, Learner Res Inst, Cleveland, OH USA.;Cleveland Clin, Ctr Microbiome & Human Hlth, Cleveland, OH USA..
    Wang, Zeneng
    Cleveland Clin, Dept Cardiovasc & Metab Sci, Learner Res Inst, Cleveland, OH USA.;Cleveland Clin, Ctr Microbiome & Human Hlth, Cleveland, OH USA..
    Helsley, Robert N.
    Cleveland Clin, Dept Cardiovasc & Metab Sci, Learner Res Inst, Cleveland, OH USA..
    Schugar, Rebecca. C.
    Cleveland Clin, Dept Cardiovasc & Metab Sci, Learner Res Inst, Cleveland, OH USA..
    Coughlin, Taylor M.
    Univ Cincinnati, Dept Internal Med, Coll Med, Cincinnati, OH USA.;Univ Cincinnati, Div Cardiovasc Hlth & Dis, Coll Med, Cincinnati, OH USA.;Univ Cincinnati, Pathobiol & Mol Med Grad Program, Coll Med, Cincinnati, OH USA..
    Wadding-Lee, Caris
    Univ Cincinnati, Dept Internal Med, Coll Med, Cincinnati, OH USA.;Univ Cincinnati, Div Cardiovasc Hlth & Dis, Coll Med, Cincinnati, OH USA.;Univ Cincinnati, Pathobiol & Mol Med Grad Program, Coll Med, Cincinnati, OH USA..
    Fleifil, Salma
    Univ Cincinnati, Dept Internal Med, Coll Med, Cincinnati, OH USA.;Univ Cincinnati, Div Cardiovasc Hlth & Dis, Coll Med, Cincinnati, OH USA..
    Russell, Hannah M.
    Univ Cincinnati, Dept Internal Med, Coll Med, Cincinnati, OH USA.;Univ Cincinnati, Div Cardiovasc Hlth & Dis, Coll Med, Cincinnati, OH USA.;Univ Cincinnati, Pathobiol & Mol Med Grad Program, Coll Med, Cincinnati, OH USA..
    Stone, Timothy
    Univ Cincinnati, Dept Environm Hlth, Coll Med, Cincinnati, OH USA.;Univ Cincinnati, Div Biostat & Bioinformat, Coll Med, Cincinnati, OH USA..
    Brooks, Michael
    Univ Cincinnati, Dept Internal Med, Coll Med, Cincinnati, OH USA.;Univ Cincinnati, Div Cardiovasc Hlth & Dis, Coll Med, Cincinnati, OH USA..
    Buffa, Jennifer A.
    Cleveland Clin, Dept Cardiovasc & Metab Sci, Learner Res Inst, Cleveland, OH USA.;Cleveland Clin, Ctr Microbiome & Human Hlth, Cleveland, OH USA..
    Mani, Kevin
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Björck, Martin
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Wanhainen, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Sangwan, Naseer
    Cleveland Clin, Dept Cardiovasc & Metab Sci, Learner Res Inst, Cleveland, OH USA.;Cleveland Clin, Ctr Microbiome & Human Hlth, Cleveland, OH USA..
    Biddinger, Sudha
    Harvard Med Sch, Boston Childrens Hosp, Div Endocrinol, Boston, MA USA..
    Bhandari, Rohan
    Cleveland Clin, Dept Cardiovasc & Metab Sci, Learner Res Inst, Cleveland, OH USA.;Cleveland Clin, Heart Vasc & Thorac Inst, Dept Cardiovasc Med, Cleveland, OH USA..
    Ademoya, Akiirayi
    Cleveland Clin, Dept Cardiovasc & Metab Sci, Learner Res Inst, Cleveland, OH USA..
    Pascual, Crystal
    Cleveland Clin, Dept Cardiovasc & Metab Sci, Learner Res Inst, Cleveland, OH USA..
    Tang, W. H. Wilson
    Cleveland Clin, Dept Cardiovasc & Metab Sci, Learner Res Inst, Cleveland, OH USA.;Cleveland Clin, Ctr Microbiome & Human Hlth, Cleveland, OH USA.;Cleveland Clin, Heart Vasc & Thorac Inst, Dept Cardiovasc Med, Cleveland, OH USA..
    Tranter, Michael
    Univ Cincinnati, Dept Internal Med, Coll Med, Cincinnati, OH USA.;Univ Cincinnati, Div Cardiovasc Hlth & Dis, Coll Med, Cincinnati, OH USA.;Univ Cincinnati, Pathobiol & Mol Med Grad Program, Coll Med, Cincinnati, OH USA..
    Cameron, Scott J.
    Cleveland Clin, Dept Cardiovasc & Metab Sci, Learner Res Inst, Cleveland, OH USA.;Cleveland Clin, Heart Vasc & Thorac Inst, Dept Cardiovasc Med, Cleveland, OH USA..
    Brown, J. Mark
    Cleveland Clin, Dept Cardiovasc & Metab Sci, Learner Res Inst, Cleveland, OH USA.;Cleveland Clin, Ctr Microbiome & Human Hlth, Cleveland, OH USA..
    Hazen, Stanley L.
    Cleveland Clin, Dept Cardiovasc & Metab Sci, Learner Res Inst, Cleveland, OH USA.;Cleveland Clin, Ctr Microbiome & Human Hlth, Cleveland, OH USA.;Cleveland Clin, Heart Vasc & Thorac Inst, Dept Cardiovasc Med, Cleveland, OH USA..
    Owens, A. Phillip, III
    Univ Cincinnati, Dept Internal Med, Coll Med, Cincinnati, OH USA.;Univ Cincinnati, Div Cardiovasc Hlth & Dis, Coll Med, Cincinnati, OH USA.;Univ Cincinnati, Pathobiol & Mol Med Grad Program, Coll Med, Cincinnati, OH USA..
    Gut Microbiota-Derived Trimethylamine N-Oxide Contributes to Abdominal Aortic Aneurysm Through Inflammatory and Apoptotic Mechanisms2023In: Circulation, ISSN 0009-7322, E-ISSN 1524-4539, Vol. 147, no 14, p. 1079-1096Article in journal (Refereed)
    Abstract [en]

    Background:Large-scale human and mechanistic mouse studies indicate a strong relationship between the microbiome-dependent metabolite trimethylamine N-oxide (TMAO) and several cardiometabolic diseases. This study aims to investigate the role of TMAO in the pathogenesis of abdominal aortic aneurysm (AAA) and target its parent microbes as a potential pharmacological intervention.

    Methods:TMAO and choline metabolites were examined in plasma samples, with associated clinical data, from 2 independent patient cohorts (N=2129 total). Mice were fed a high-choline diet and underwent 2 murine AAA models, angiotensin II infusion in low-density lipoprotein receptor-deficient (Ldlr(-/-)) mice or topical porcine pancreatic elastase in C57BL/6J mice. Gut microbial production of TMAO was inhibited through broad-spectrum antibiotics, targeted inhibition of the gut microbial choline TMA lyase (CutC/D) with fluoromethylcholine, or the use of mice genetically deficient in flavin monooxygenase 3 (Fmo3(-/-)). Finally, RNA sequencing of in vitro human vascular smooth muscle cells and in vivo mouse aortas was used to investigate how TMAO affects AAA.

    Results:Elevated TMAO was associated with increased AAA incidence and growth in both patient cohorts studied. Dietary choline supplementation augmented plasma TMAO and aortic diameter in both mouse models of AAA, which was suppressed with poorly absorbed oral broad-spectrum antibiotics. Treatment with fluoromethylcholine ablated TMAO production, attenuated choline-augmented aneurysm initiation, and halted progression of an established aneurysm model. In addition, Fmo3(-/-) mice had reduced plasma TMAO and aortic diameters and were protected from AAA rupture compared with wild-type mice. RNA sequencing and functional analyses revealed choline supplementation in mice or TMAO treatment of human vascular smooth muscle cells-augmented gene pathways associated with the endoplasmic reticulum stress response, specifically the endoplasmic reticulum stress kinase PERK.

    Conclusions:These results define a role for gut microbiota-generated TMAO in AAA formation through upregulation of endoplasmic reticulum stress-related pathways in the aortic wall. In addition, inhibition of microbiome-derived TMAO may serve as a novel therapeutic approach for AAA treatment where none currently exist.

  • 26.
    Benson, Tyler W.
    et al.
    Division of Cardiovascular Health and Disease, University of Cincinnati College of Medicine, OH, Cincinnati, United States.
    Pike, Mindy M.
    Division of Epidemiology, Vanderbilt Genetics Institute, Institute of Medicine and Public Health, TN, Nashville, United States; Division of Nephrology and Hypertension, Center for Kidney Disease, Vanderbilt University Medical Center, TN, Nashville, United States.
    Spuzzillo, Anthony
    Division of Cardiovascular Health and Disease, University of Cincinnati College of Medicine, OH, Cincinnati, United States; Departments of Internal Medicine and Pathology and Laboratory Medicine, Pathobiology and Molecular Medicine Graduate Program, University of Cincinnati, OH, Cincinnati, United States.
    Hicks, Sarah M.
    Division of Genome Science and Cancer, John Curtin School of Medical Research, Australian National University, Canberra, Australia.
    Ali, Sidra
    Division of Genome Science and Cancer, John Curtin School of Medical Research, Australian National University, Canberra, Australia.
    Pham, Michael
    Department of Cardiovascular Medicine, Section of Vascular Medicine, Heart and Vascular Institute, Cleveland Clinic Foundation, OH, Cleveland, United States.
    Mix, Doran S.
    Division of Vascular Surgery, Department of Surgery, University of Rochester School of Medicine, NY, Rochester, United States.
    Brunner, Seth I.
    Division of Cardiovascular Health and Disease, University of Cincinnati College of Medicine, OH, Cincinnati, United States.
    Wadding-Lee, Caris
    Division of Cardiovascular Health and Disease, University of Cincinnati College of Medicine, OH, Cincinnati, United States; Departments of Internal Medicine and Pathology and Laboratory Medicine, Pathobiology and Molecular Medicine Graduate Program, University of Cincinnati, OH, Cincinnati, United States.
    Conrad, Kelsey A.
    Division of Cardiovascular Health and Disease, University of Cincinnati College of Medicine, OH, Cincinnati, United States; Departments of Internal Medicine and Pathology and Laboratory Medicine, Pathobiology and Molecular Medicine Graduate Program, University of Cincinnati, OH, Cincinnati, United States.
    Russell, Hannah M.
    Division of Cardiovascular Health and Disease, University of Cincinnati College of Medicine, OH, Cincinnati, United States; Departments of Internal Medicine and Pathology and Laboratory Medicine, Pathobiology and Molecular Medicine Graduate Program, University of Cincinnati, OH, Cincinnati, United States.
    Jennings, Courtney
    Department of Cardiovascular Medicine, Section of Vascular Medicine, Heart and Vascular Institute, Cleveland Clinic Foundation, OH, Cleveland, United States.
    Coughlin, Taylor M.
    Division of Cardiovascular Health and Disease, University of Cincinnati College of Medicine, OH, Cincinnati, United States; Departments of Internal Medicine and Pathology and Laboratory Medicine, Pathobiology and Molecular Medicine Graduate Program, University of Cincinnati, OH, Cincinnati, United States.
    Aggarwal, Anu
    Department of Cardiovascular and Metabolic Sciences, Lerner Research Institute, Cleveland Clinic Foundation, OH, Cleveland, United States.
    Lyden, Sean
    Department of Cardiovascular Medicine, Section of Vascular Medicine, Heart and Vascular Institute, Cleveland Clinic Foundation, OH, Cleveland, United States.
    Mani, Kevin
    Department of Surgical Sciences, Vascular Surgery, Uppsala University, Uppsala, Sweden.
    Björck, Martin
    Department of Surgical Sciences, Vascular Surgery, Uppsala University, Uppsala, Sweden.
    Wanhainen, Anders
    Umeå University, Faculty of Medicine, Department of Surgical and Perioperative Sciences, Surgery. Umeå University, Faculty of Medicine, Department of Diagnostics and Intervention. Department of Surgical Sciences, Vascular Surgery, Uppsala University, Uppsala, Sweden.
    Bhandari, Rohan
    Department of Cardiovascular Medicine, Section of Vascular Medicine, Heart and Vascular Institute, Cleveland Clinic Foundation, OH, Cleveland, United States; Department of Cardiovascular and Metabolic Sciences, Lerner Research Institute, Cleveland Clinic Foundation, OH, Cleveland, United States.
    Lipworth-Elliot, Loren
    Division of Epidemiology, Vanderbilt Genetics Institute, Institute of Medicine and Public Health, TN, Nashville, United States; Division of Nephrology and Hypertension, Center for Kidney Disease, Vanderbilt University Medical Center, TN, Nashville, United States.
    Robinson-Cohen, Cassianne
    Division of Nephrology and Hypertension, Center for Kidney Disease, Vanderbilt University Medical Center, TN, Nashville, United States; Vanderbilt-O'Brien Center for Kidney Disease, Vanderbilt University Medical Center, TN, Nashville, United States.
    Caputo, Francis J.
    Department of Cardiovascular Medicine, Section of Vascular Medicine, Heart and Vascular Institute, Cleveland Clinic Foundation, OH, Cleveland, United States.
    Shim, Sharon
    Department of Cardiovascular Medicine, Section of Vascular Medicine, Heart and Vascular Institute, Cleveland Clinic Foundation, OH, Cleveland, United States.
    Quesada, Odayme
    Women's Heart Center, The Christ Hospital Heart and Vascular Institute, OH, Cincinnati, United States; The Carl and Edyth Lindner Center for Research and Education, The Christ Hospital, OH, Cincinnati, United States.
    Tourdot, Benjamin
    Division of Experimental Hematology and Cancer Biology, Cincinnati Children's Hospital Medical Center, OH, Cincinnati, United States.
    Edwards, Todd L.
    Division of Epidemiology, Vanderbilt Genetics Institute, Institute of Medicine and Public Health, TN, Nashville, United States.
    Tranter, Michael
    Division of Cardiovascular Health and Disease, University of Cincinnati College of Medicine, OH, Cincinnati, United States.
    Gardiner, Elizabeth E.
    Division of Genome Science and Cancer, John Curtin School of Medical Research, Australian National University, Canberra, Australia.
    Mackman, Nigel
    Division of Hematology and Oncology, Department of Medicine, The University of North Carolina at Chapel Hill, NC, Chapel Hill, United States.
    Cameron, Scott J.
    Department of Cardiovascular Medicine, Section of Vascular Medicine, Heart and Vascular Institute, Cleveland Clinic Foundation, OH, Cleveland, United States; Department of Cardiovascular and Metabolic Sciences, Lerner Research Institute, Cleveland Clinic Foundation, OH, Cleveland, United States; Department of Hematology, Taussig Cancer Institute, Cleveland Clinic Foundation, OH, Cleveland, United States.
    Owens, A. Phillip
    Division of Cardiovascular Health and Disease, University of Cincinnati College of Medicine, OH, Cincinnati, United States.
    Soluble glycoprotein VI predicts abdominal aortic aneurysm growth rate and is a novel therapeutic target2024In: Blood, ISSN 0006-4971, E-ISSN 1528-0020, Vol. 144, no 16, p. 1663-1678Article in journal (Refereed)
    Abstract [en]

    A common feature in patients with abdominal aortic aneurysms (AAAs) is the formation of a nonocclusive intraluminal thrombus (ILT) in regions of aortic dilation. Platelets are known to maintain hemostasis and propagate thrombosis through several redundant activation mechanisms, yet the role of platelet activation in the pathogenesis of AAA-associated ILT is still poorly understood. Thus, we sought to investigate how platelet activation affects the pathogenesis of AAA. Using RNA sequencing, we identified that the platelet-associated transcripts are significantly enriched in the ILT compared with the adjacent aneurysm wall and healthy control aortas. We found that the platelet-specific receptor glycoprotein VI (GPVI) is among the top enriched genes in AAA ILT and is increased on the platelet surface of patients with AAAs. Examination of a specific indicator of platelet activity, soluble GPVI (sGPVI), in 2 independent cohorts of patients with AAAs is highly predictive of an AAA diagnosis and associates more strongly with aneurysm growth rate than D-dimer in humans. Finally, intervention with the anti-GPVI antibody (JAQ1) in mice with established aneurysms blunted the progression of AAA in 2 independent mouse models. In conclusion, we show that the levels of sGPVI in humans can predict a diagnosis of AAA and AAA growth rate, which may be critical in the identification of high-risk patients. We also identify GPVI as a novel platelet-specific AAA therapeutic target, with minimal risk of adverse bleeding complications, for which none currently exists.

  • 27.
    Benson, Tyler W.
    et al.
    Univ Cincinnati, Coll Med, Div Cardiovasc Hlth & Dis, Cincinnati, OH USA..
    Pike, Mindy M.
    Vanderbilt Genet Inst, Inst Med & Publ Hlth, Div Epidemiol, Nashville, TN USA.;Vanderbilt Univ, Ctr Kidney Dis, Med Ctr, Div Nephrol & Hypertens, Nashville, TN USA..
    Spuzzillo, Anthony
    Univ Cincinnati, Coll Med, Div Cardiovasc Hlth & Dis, Cincinnati, OH USA.;Univ Cincinnati, Dept Internal Med, Grad Program, Cincinnati, OH USA.;Univ Cincinnati, Dept Pathol & Lab Med, Grad Program, Cincinnati, OH USA.;Univ Cincinnati, Dept Pathobiol & Mol Med, Grad Program, Cincinnati, OH USA..
    Hicks, Sarah M.
    Australian Natl Univ, John Curtin Sch Med Res, Div Genome Sci & Canc, Canberra, Australia..
    Ali, Sidra
    Australian Natl Univ, John Curtin Sch Med Res, Div Genome Sci & Canc, Canberra, Australia..
    Pham, Michael
    Cleveland Clin Fdn, Heart & Vasc Inst, Dept Cardiovasc Med, Sect Vasc Med, Cleveland, OH USA..
    Mix, Doran S.
    Univ Rochester, Sch Med & Dent, Dept Surg, Div Vasc Surg, Rochester, NY USA..
    Brunner, Seth I.
    Univ Cincinnati, Coll Med, Div Cardiovasc Hlth & Dis, Cincinnati, OH USA..
    Wadding-Lee, Caris
    Univ Cincinnati, Coll Med, Div Cardiovasc Hlth & Dis, Cincinnati, OH USA.;Univ Cincinnati, Dept Internal Med, Grad Program, Cincinnati, OH USA.;Univ Cincinnati, Dept Pathol & Lab Med, Grad Program, Cincinnati, OH USA.;Univ Cincinnati, Dept Pathobiol & Mol Med, Grad Program, Cincinnati, OH USA..
    Conrad, Kelsey A.
    Univ Cincinnati, Coll Med, Div Cardiovasc Hlth & Dis, Cincinnati, OH USA.;Univ Cincinnati, Dept Internal Med, Grad Program, Cincinnati, OH USA.;Univ Cincinnati, Dept Pathol & Lab Med, Grad Program, Cincinnati, OH USA.;Univ Cincinnati, Dept Pathobiol & Mol Med, Grad Program, Cincinnati, OH USA..
    Russell, Hannah M.
    Univ Cincinnati, Coll Med, Div Cardiovasc Hlth & Dis, Cincinnati, OH USA.;Univ Cincinnati, Dept Internal Med, Grad Program, Cincinnati, OH USA.;Univ Cincinnati, Dept Pathol & Lab Med, Grad Program, Cincinnati, OH USA.;Univ Cincinnati, Dept Pathobiol & Mol Med, Grad Program, Cincinnati, OH USA..
    Jennings, Courtney
    Cleveland Clin Fdn, Heart & Vasc Inst, Dept Cardiovasc Med, Sect Vasc Med, Cleveland, OH USA..
    Coughlin, Taylor M.
    Univ Cincinnati, Coll Med, Div Cardiovasc Hlth & Dis, Cincinnati, OH USA.;Univ Cincinnati, Dept Internal Med, Grad Program, Cincinnati, OH USA.;Univ Cincinnati, Dept Pathol & Lab Med, Grad Program, Cincinnati, OH USA.;Univ Cincinnati, Dept Pathobiol & Mol Med, Grad Program, Cincinnati, OH USA..
    Aggarwal, Anu
    Cleveland Clin Fdn, Lerner Res Inst, Dept Cardiovasc & Metab Sci, Cleveland, OH USA..
    Lyden, Sean
    Cleveland Clin Fdn, Heart & Vasc Inst, Dept Cardiovasc Med, Sect Vasc Med, Cleveland, OH USA..
    Mani, Kevin
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Björck, Martin
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Wanhainen, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery. Umeå Univ, Dept Surg & Perioperat Sci, Umeå, Sweden..
    Bhandari, Rohan
    Cleveland Clin Fdn, Heart & Vasc Inst, Dept Cardiovasc Med, Sect Vasc Med, Cleveland, OH USA.;Cleveland Clin Fdn, Lerner Res Inst, Dept Cardiovasc & Metab Sci, Cleveland, OH USA..
    Lipworth-Elliot, Loren
    Vanderbilt Genet Inst, Inst Med & Publ Hlth, Div Epidemiol, Nashville, TN USA.;Vanderbilt Univ, Ctr Kidney Dis, Med Ctr, Div Nephrol & Hypertens, Nashville, TN USA..
    Robinson-Cohen, Cassianne
    Vanderbilt Univ, Ctr Kidney Dis, Med Ctr, Div Nephrol & Hypertens, Nashville, TN USA.;Vanderbilt Univ, Vanderbilt OBrien Ctr Kidney Dis, Med Ctr, Nashville, TN USA..
    Caputo, Francis J.
    Cleveland Clin Fdn, Heart & Vasc Inst, Dept Cardiovasc Med, Sect Vasc Med, Cleveland, OH USA..
    Shim, Sharon
    Cleveland Clin Fdn, Heart & Vasc Inst, Dept Cardiovasc Med, Sect Vasc Med, Cleveland, OH USA..
    Quesada, Odayme
    Christ Hosp, Heart & Vasc Inst, Womens Heart Ctr, Cincinnati, OH USA.;Christ Hosp, Carl & Edyth Lindner Ctr Res & Educ, Cincinnati, OH USA..
    Tourdot, Benjamin
    Cincinnati Childrens Hosp, Med Ctr, Div Expt Hematol & Canc Biol, Cincinnati, OH USA..
    Edwards, Todd L.
    Vanderbilt Genet Inst, Inst Med & Publ Hlth, Div Epidemiol, Nashville, TN USA..
    Tranter, Michael
    Univ Cincinnati, Coll Med, Div Cardiovasc Hlth & Dis, Cincinnati, OH USA..
    Gardiner, Elizabeth E.
    Australian Natl Univ, John Curtin Sch Med Res, Div Genome Sci & Canc, Canberra, Australia..
    Mackman, Nigel
    Univ North Carolina Chapel Hill, Dept Med, Div Hematol & Oncol, Chapel Hill, NC USA..
    Cameron, Scott J.
    Cleveland Clin Fdn, Heart & Vasc Inst, Dept Cardiovasc Med, Sect Vasc Med, Cleveland, OH USA.;Cleveland Clin Fdn, Lerner Res Inst, Dept Cardiovasc & Metab Sci, Cleveland, OH USA.;Cleveland Clin Fdn, Taussig Canc Inst, Dept Hematol, Cleveland, OH USA..
    Owens III, A. Phillip
    Soluble glycoprotein VI predicts abdominal aortic aneurysm growth rate and is a novel therapeutic target2024In: Blood, ISSN 0006-4971, E-ISSN 1528-0020, Vol. 144, no 16, p. 1663-1678Article in journal (Refereed)
    Abstract [en]

    A common feature in patients with abdominal aortic aneurysms (AAAs) is the formation of a nonocclusive intraluminal thrombus (ILT) in regions of aortic dilation. Platelets are known to maintain hemostasis and propagate thrombosis through several redundant activation mechanisms, yet the role of platelet activation in the pathogenesis of AAA-associated ILT is still poorly understood. Thus, we sought to investigate how platelet activation affects the pathogenesis of AAA. Using RNA sequencing, we identified that the platelet-associated transcripts are significantly enriched in the ILT compared with the adjacent aneurysm wall and healthy control aortas. We found that the platelet-specific receptor glycoprotein VI (GPVI) is among the top enriched genes in AAA ILT and is increased on the platelet surface of patients with AAAs. Examination of a specific indicator of platelet activity, soluble GPVI (sGPVI), in 2 independent cohorts of patients with AAAs is highly predictive of an AAA diagnosis and associates more strongly with aneurysm growth rate than D-dimer in humans. Finally, intervention with the anti-GPVI antibody (JAQ1) in mice with established aneurysms blunted the progression of AAA in 2 independent mouse models. In conclusion, we show that the levels of sGPVI in humans can predict a diagnosis of AAA and AAA growth rate, which may be critical in the identification of high-risk patients. We also identify GPVI as a novel platelet- specific AAA therapeutic target, with minimal risk of adverse bleeding complications, for which none currently exists.

  • 28.
    Bergqvist, David
    et al.
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences.
    Björck, Martin
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences.
    Ljungman, Christer
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences.
    Nyman, Rickard
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Oncology, Radiology and Clinical Immunology, Radiology.
    Wanhainen, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences.
    Treatment options for abdominal aortic aneurysm (AAA)2006In: Vascular Surgery / [ed] Alun H. Davies, London: Springer , 2006Chapter in book (Other academic)
  • 29.
    Bergqvist, David
    et al.
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Björck, Martin
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Ljungman, Christer
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Nyman, Rickard
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Radiology, Oncology and Radiation Science, Radiology.
    Wanhainen, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Treatment options for abdominal aortic aneurysm (AAA)2007In: Vascular surgery / [ed] C.D. Liapsis, K. Baltzer, F. Benedetti-Valentini, J. Fernandes e Fernandes, Berlin Heidelberg New York: Springer , 2007, p. 325-329Chapter in book (Refereed)
  • 30.
    Bergqvist, David
    et al.
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Björck, Martin
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Wanhainen, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Abdominal aortic aneurysm and new WHO criteria for screening2013In: International Journal of Angiology, ISSN 0392-9590, E-ISSN 1827-1839, Vol. 32, no 1, p. 37-41Article, review/survey (Refereed)
    Abstract [en]

    Does screening of abdominal aortic aneurysm (AAA) fulfil the recently revised the World Health Organization WHO criteria for screening? Contemporary data from the literature are used to analyze whether the ten recent WHO criteria can be used to motivate AAA screening. Although the prevalence of AAA seems to decrease, at least screening of 65-year old males saves lives and is cost-effective. Ultrasonographic screening for AAA in risk populations fulfils the new WHO criteria for screening.

  • 31.
    Bergqvist, David
    et al.
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Björck, Martin
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Wanhainen, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Abdominal aortic aneurysm--to screen or not to screen2008In: European Journal of Vascular and Endovascular Surgery, ISSN 1078-5884, E-ISSN 1532-2165, Vol. 35, no 1, p. 13-18Article in journal (Refereed)
    Abstract [en]

    With the ten WHO criteria for a screening program to be started, screening for abdominal aortic aneurysm is analyzed. Most of the criteria are fulfilled concerning the 65-year old male population, whereas concerning females we need more knowledge. Still the aneurysmal diameter is the most important factor to select patients for treatment meaning that many aneurysms are treated where rupture should never have occurred. Research projects giving more information on pathophysiological processes behind expansion and rupture should have priority.

  • 32.
    Bergqvist, David
    et al.
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Björck, Martin
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Wanhainen, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Treatment of vascular Ehlers-Danlos syndrome: a systematic review2013In: Annals of Surgery, ISSN 0003-4932, E-ISSN 1528-1140, Vol. 258, no 2, p. 257-261Article in journal (Refereed)
    Abstract [en]

    OBJECTIVE:

    To provide the collected evidence from all literature reports.

    BACKGROUND:

    Vascular Ehlers-Danlos syndrome (EDS) is a rare connective tissue disorder with serious hemorrhagic consequences. Most experience on treatment is based on case reports and small case series.

    METHOD:

    A systematic literature review was performed. PubMed and reference lists were scrutinized.

    RESULTS:

    A total of 231 patients were identified with no gender preponderance. Aneurysms were present in 40%, often multiple. In 33%, there was an arterial rupture without an underlying aneurysm. Carotidocavernous fistula was seen in 18%. After open surgery the mortality was 30%; after endovascular procedures, it was 24%; in a group of miscellaneous cases, it was 60%; and the overall mortality was 39%. The median age of patients at death was 31 years. The median follow-up time was 12 months (5 days-7 years), but in 20% cases, it was not reported. In only 29 of the 119 recent patients (24%) the mutation was verified with molecular genetic testing.

    CONCLUSIONS:

    Vascular EDS is a serious disorder with high mortality, which does not seem to have been influenced by new treatment methods. Invasive methods should be used only when necessary, primarily to save the patients' life. Whenever possible, the genetic molecular defect should be identified. The results of this review may be affected by publications bias. Ideally, a prospective registry should be created.

  • 33.
    Bergqvist, David
    et al.
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Mani, Kevin
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Troëng, Thomas
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Wanhainen, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Treatment of aortic aneurysms registered in Swedvasc: Development reflected in a national vascular registry with an almost 100% coverage2018In: Gefässchirurgie, ISSN 0948-7034, E-ISSN 1434-3932, Vol. 23, no 5, p. 340-345Article in journal (Refereed)
    Abstract [en]

    Swedvasc is a registry for vascular surgical procedures, both open and endovascular. It was started in 1987 and since 1994 the whole population of Sweden is covered, at present around 10 million inhabitants. In a recent external validation, it was found to be highly accurate with abdominal aortic aneurysm surgery correctly reported in > 96%. In this paper various factors explaining the almost 100% coverage are discussed, one important being that the registry has been developed and maintained within the profession of vascular surgery and not dictated by authorities. Another factor of importance is the possibility to use data in various research projects and so far 15 PhD theses have used Swedvasc data. To exemplify the practical use of the registry, the treatment of abdominal aortic aneurysms is scrutinized and among the various complications abdominal compartment syndrome is analyzed. Several significant temporal changes have been observed over the almost 25 years of Swedvasc: increasing use of endovascular surgery, treatment of aneurysms detected by screening , decreasing treatment for rupture, improved outcome, increasing treatment of older patients and patients with comorbid conditions. In conclusion, a high quality national vascular registry can be valid with high compliance and can be used to study population-based development of treatment and outcome. It can also be used to perform international comparisons with other registries, thereby getting an indication of the quality of care.

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  • 34.
    Bergqvist, David
    et al.
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Mani, Kevin
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Wanhainen, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Epidemiological aspects on abdominal aortic aneurysm (AAA)2010In: Pan Arab Angiology Journal, ISSN 2000-6535, Vol. 1, p. 1-Article in journal (Refereed)
    Abstract [en]

    In this overview, the present day knowledge on the epidemiology of abdominal aortic aneurysms (AAA) is summarized based on a review of the current literature. The prevalence of AAA and incidence of rupture is analyzed, and the natural history of the disease is illustrated both concerning the AAA as such and the survival of the patient. This knowledge is important when contemplating on screening for AAA, which is being implemented in several countries worldwide.

  • 35.
    Bergqvist, David
    et al.
    Uppsala University, Medicinska vetenskapsområdet, Faculty of Medicine, Department of Surgical Sciences.
    Wanhainen, Anders
    Uppsala University, Medicinska vetenskapsområdet, Faculty of Medicine, Department of Surgical Sciences.
    Abdominal aortic aneurysm2007In: European Manual in Medicine, 2007Chapter in book (Refereed)
  • 36.
    Bergqvist, David
    et al.
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Wanhainen, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Cerebrospinal venös insufficiens som orsak till MS har svagt stöd. Inte rimligt att nu erbjuda ballongvidgande behandling: [Cerebrospinal venous insufficiency as a cause of MS weakly supported. Unreasonable to offer balloon dilatation therapy now].2011In: Läkartidningen, ISSN 0023-7205, E-ISSN 1652-7518, Vol. 108, no 39, p. 1899-1901Article in journal (Refereed)
    Abstract [en]

    Chronic cerebrospinal venous insufficiency (CCSVI) has been suggested as a hypothesis explaining the development of multiple sclerosis (MS). In case reports, balloon dilatation of obstructed venous outflow has been successful and enthusiastic patient histories have given hope to MS patients. A systematic review of the evidence behind the pathophysiological hypothesis as well as concerning balloon dilatation does not support this form of treatment outside well designed trials.

  • 37.
    Bergqvist, David
    et al.
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Wanhainen, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Konsten att skriva ett vetenskapligt manus2015In: Svensk Kirurgi, ISSN 0346-847X, Vol. 73, no 1, p. 10-12Article in journal (Other academic)
  • 38. Bissacco, Daniele
    et al.
    Mandigers, Tim J
    Savaré, Laura
    Domanin, Maurizio
    D'Oria, Mario
    Ieva, Francesca
    Van Herwaarden, Joost A
    Mani, Kevin
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Wanhainen, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Trimarchi, Santi
    Comparison of the Reproducibility of Ultrasound Calliper Placement Methods in Abdominal Aortic Diameter Measurements: A Systematic Review and Meta-Analysis of Diagnostic Test Accuracy Studies2023In: European Journal of Vascular and Endovascular Surgery, ISSN 1078-5884, E-ISSN 1532-2165, Vol. 66, no 5, p. 620-631Article in journal (Refereed)
    Abstract [en]

    OBJECTIVE: To assess which ultrasound (US) method of maximum anteroposterior (AP) abdominal aortic diameter measurement can be considered most reproducible.

    DATA SOURCES: MEDLINE, Scopus, and Web of Science were searched (PROSPERO ID: 276694). Eligible studies reported intra- and or interobserver agreement according to Bland-Altman analysis (mean ± standard deviation [SD]) for abdominal aortic diameter AP US evaluations with an outer to outer (OTO), inner to inner (ITI), and or leading edge to leading edge (LELE) calliper placement.

    REVIEW METHODS: The Preferred Reporting Items for a Systematic Review and Meta-Analysis of Diagnostic Test Accuracy Studies statement was followed. The QUADAS-2 tool and QUADAS-C extension were used for risk of bias assessment and the GRADE framework to rate the certainty of evidence. Pooled estimates (fixed effects meta-analysis, after a test of homogeneity of means) for each US method were compared with pairwise one sided t tests. Sensitivity analyses (for studies published in 2010 or later) and meta-regression were also performed.

    RESULTS: 21 studies were included in the qualitative analysis. Twelve were eligible for quantitative analysis. Studies showed heterogeneity in the US model and transducer used, sex of participants, and observer professions, expertise, and training. Included studies shared a common mean for each US method (OTO: p = 1.0, ITI: p = 1.0, and LELE: p = 1.0). A pooled estimate of interobserver reproducibility for each US method was obtained, combining the mean ± SD (Bland-Altman analysis) from each study: OTO: 0.182 ± 0.440; ITI: 0.170 ± 0.554; and LELE: 0.437 ± 0.419. There were no statistically significant differences between the methods (OTO vs. ITI: p = .52, OTO vs. LELE: p = .069, ITI vs. LELE: p = .17). Considering studies published in 2010 and later, the pooled estimate for LELE was the smallest, without statistically significant differences between the methods. Despite the low risk of bias, the certainty of the evidence for both meta-analysed outcomes remained low.

    CONCLUSION: The interobserver reproducibility for OTO and ITI was 2.5 times smaller (indicating better reproducibility) than LELE; however, without statistically significant differences between the methods and low GRADE evidence certainty. Additional data are needed to validate these findings, while inherent differences between the methods need to be emphasised.

  • 39. Bjarnason, Thordur
    et al.
    Montgomery, A.
    Ekberg, O.
    Acosta, S.
    Svensson, M.
    Wanhainen, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Björck, Martin
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Petersson, U.
    One-Year Follow-up After Open Abdomen Therapy With Vacuum-Assisted Wound Closure and Mesh-Mediated Fascial Traction2013In: World Journal of Surgery, ISSN 0364-2313, E-ISSN 1432-2323, Vol. 37, no 9, p. 2031-2038Article in journal (Refereed)
    Abstract [en]

    Open abdomen (OA) therapy frequently results in a giant planned ventral hernia. Vacuum-assisted wound closure and mesh-mediated fascial traction (VAWCM) enables delayed primary fascial closure in most patients, even after prolonged OA treatment. Our aim was to study the incidence of hernia and abdominal wall discomfort 1 year after abdominal closure. A prospective multicenter cohort study of 111 patients undergoing OA/VAWCM was performed during 2006-2009. Surviving patients underwent clinical examination, computed tomography (CT), and chart review at 1 year. Incisional and parastomal hernias and abdominal wall symptoms were noted. The median age for the 70 surviving patients was 68 years, 77 % of whom were male. Indications for OA were visceral pathology (n = 40), vascular pathology (n = 22), or trauma (n = 8). Median length of OA therapy was 14 days. Among 64 survivors who had delayed primary fascial closure, 23 (36 %) had a clinically detectable hernia and another 19 (30 %) had hernias that were detected on CT (n = 18) or at laparotomy (n = 1). Symptomatic hernias were found in 14 (22 %), 7 of them underwent repair. The median hernia widths in symptomatic and asymptomatic patients were 7.3 and 4.8 cm, respectively (p = 0.031) with median areas of 81.0 and 42.9 cm(2), respectively (p = 0.025). Of 31 patients with a stoma, 18 (58 %) had a parastomal hernia. Parastomal hernia (odds ratio 8.9; 95 % confidence interval 1.2-68.8) was the only independent factor associated with an incisional hernia. Incisional hernia incidence 1 year after OA therapy with VAWCM was high. Most hernias were small and asymptomatic, unlike the giant planned ventral hernias of the past.

  • 40.
    Björck, M
    et al.
    Uppsala University, Medicinska vetenskapsområdet, Faculty of Medicine, Department of Surgical Sciences.
    Wanhainen, A
    Uppsala University, Medicinska vetenskapsområdet, Faculty of Medicine, Department of Surgical Sciences.
    Invited commentary for: the uncertainty of help versus harm in treatment of asymptomatic aortic aneurysms2006In: Eur J Vasc Endovasc Surg, ISSN 1078-5884, Vol. 32, no 6, p. 624-6Article in journal (Refereed)
  • 41.
    Björck, Martin
    et al.
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Bown, M J
    Choke, E
    Earnshaw, J
    Flørenes, T
    Glover, M
    Kay, M
    Laukontaus, S
    Lees, T
    Lindholt, J
    Powell, J T
    van Rij, A
    Svensjö, Sverker
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Wanhainen, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    International update on screening for abdominal aortic aneurysms: issues and opportunities.2015In: European Journal of Vascular and Endovascular Surgery, ISSN 1078-5884, E-ISSN 1532-2165, Vol. 49, no 2Article in journal (Refereed)
  • 42.
    Björck, Martin
    et al.
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Djavani, Khatereh
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Wanhainen, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Valtysson, Johann
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Colonic ischaemia and intra-abdominal hypertension following open repair of ruptured abdominal aortic aneurysm (Br J Surg 2009; 96:621-627) Reply2009In: British Journal of Surgery, ISSN 0007-1323, E-ISSN 1365-2168, Vol. 96, no 8, p. 959-960Article in journal (Refereed)
  • 43.
    Björck, Martin
    et al.
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Djavani-Gidlund, Khatereh
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Wanhainen, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Response to comment on "Intraabdominal hypertension and abdominal compartment syndrome after endovascular repair of ruptured abdominal aortic aneurysm"2012In: European Journal of Vascular and Endovascular Surgery, ISSN 1078-5884, E-ISSN 1532-2165, Vol. 43, no 1, p. 132-132Article in journal (Refereed)
  • 44.
    Björck, Martin
    et al.
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Gottsäter, A
    Bergqvist, David
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Wanhainen, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    The importance of statins, smoking, hypertension and life style control2012In: 34th Symposium Book: Vascular and Endovascular Controversies Update / [ed] Roger M Greenhalgh, London: BIBA Publishing , 2012, , p. 291-97p. 291-297Chapter in book (Other academic)
  • 45.
    Björck, Martin
    et al.
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Hägg, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Medical Sciences, Internal Medicine.
    Wanhainen, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Hellström Pigg, Maritta
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Immunology, Genetics and Pathology, Medical Genetics.
    Bergqvist, David
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Nya behandlingsmöjligheter vid vaskulärt Ehlers: Danlos syndrom2013In: Läkartidningen, ISSN 0023-7205, E-ISSN 1652-7518, Vol. 110, no 29-31, p. 1354-1355Article in journal (Other academic)
    Abstract [sv]

    Vaskulärt Ehlers–Danlos syndrom (VED) är en mycket ovanlig, autosomalt dominant nedärvd, sjukdom. Endast ca 50 individer i Sverige har en molekylärgenetiskt verifierad diagnos.

    En randomiserad studie visar att betablockeraren celiprolol kan förebygga kärlkatastrofer vid vaskulärt Ehlers–Danlos syndrom.

    Vid kärlkomplikationer är ­konservativ behandling första val, men det kan vara riskabelt att avstå från öppen eller endovaskulär kärlkirurgi.

    Behandling behöver ofta inledas omgående, men kontakt bör tas med ett center med erfarenhet av att behandla detta farliga och ovanliga tillstånd.

  • 46.
    Björck, Martin
    et al.
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Lepkowska Eriksson, M.
    Bylock, A.
    Steuer, Johnny
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Wanhainen, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Carlsson, B. C. L.
    Bock, D.
    Kragsterman, Björn
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Plasminogen Activator Inhibitor-1 Levels and Activity Decrease After Intervention in Patients with Critical Limb Ischaemia2013In: European Journal of Vascular and Endovascular Surgery, ISSN 1078-5884, E-ISSN 1532-2165, Vol. 46, no 2, p. 214-222Article in journal (Refereed)
    Abstract [en]

    Patients with peripheral arterial occlusive disease (PAOD), in particular critical limb ischaemia (CLI), carry a high risk of thrombotic events. We hypothesised that patients undergoing conservative, endovascular, or open surgical treatment for CLI have increased levels of plasminogen activator inhibitor-1 (PAI-1), leading to a prothrombotic state. The objective was to determine levels of PAI-1 in patients with acute or chronic PAOD/CLI. Thirty-two patients with a median age of 74 (49–90) years were included. Three underwent thrombolysis for acute limb-threatening ischaemia. Twenty-six patients with chronic ischaemia received endovascular (n = 20) or open (n = 6) surgical treatment. Three were treated conservatively. Biomarkers and ankle brachial index (ABI) were measured before and up to 1 month after intervention. Patency was studied with repeated duplex ultrasound. Ankle pressure and ABI improved after intervention (p < .001). C-reactive protein (CRP) increased from a median of 7.90 mg/L at baseline to 31.5 on day 1 (p < .001), 28.0 on day 6 (p < .001), and returned to baseline levels on day 30. PAI-1 antigen and activity decreased from day 6 and onwards post-intervention compared with baseline (p < .05). A great individual variability in PAI-1 antigen and activity was observed. Although most actively treated patients had normal PAI-1 activity, 11/29 (38%) were above that level of normality at baseline, 10/24 (42%) on day 1, 3/23 (13%) on day 6, and 5/27 (19%) on day 30 after intervention. Endovascular and open surgical treatment resulted in improved ankle pressure and ABI. The intervention was followed by a transient increase in CRP and a sustained reduction in PAI-1 levels and activity.

  • 47.
    Björck, Martin
    et al.
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Ravn, Hans
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Nilsson, T K
    Wanhainen, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Nilsson, P M
    Blood cell telomere length among patients with an isolated popliteal artery aneurysm and those with multiple aneurysm disease2011In: Atherosclerosis, ISSN 0021-9150, E-ISSN 1879-1484, Vol. 219, no 2, p. 946-950Article in journal (Refereed)
    Abstract [en]

    OBJECTIVES:

    Short relative telomere length (RTL) is associated with vascular ageing, inflammation and cardiovascular risk factors. Previous studies have reported an association between abdominal aortic aneurysm and short RTL. The presence of atherosclerosis among patients with aneurysm disease may, however, be a confounder. The aim was to explore the associations between short RTL and aneurysm disease, by comparing patients with isolated popliteal artery aneurysms with those having multiple aneurysms.

    DESIGN AND PATIENTS:

    DNA was retrieved from 183 patients with popliteal artery aneurysm (PAA). They were all examined with ultrasound at the time of blood-sampling, and had a total of 423 aneurysms (range 1-7, mean 2.3/patient).

    METHODS:

    TL was measured with Real-Time PCR, RTL was calculated by comparing with three reference populations.

    RESULTS:

    Patients with bilateral PAAs had a mean RTL of 0.985 vs. 1.038 with unilateral PAAs (P=0.326). Patients with abdominal aortic aneurysm had RTL 1.035, vs. 0.999 without (P=0.513). No difference was seen with or without femoral or iliac aneurysms. Fifty-six patients with isolated PAA at surgery and at re-examination had RTL 0.974, vs. 1.033 who had >1 aneurysm (P=0.308). RTL was not associated with the number of aneurysms at re-examination (P=0.727, one-way ANOVA). There was a trend towards shorter RTL among active smokers (0.93 vs. 1.04, P=0.066).

    CONCLUSIONS:

    No association between short RTL and multiple aneurysm disease was found. The previously reported association between AAA and short RTL may be secondary to cardiovascular risk factors, rather than by aneurysm disease.

  • 48.
    Björck, Martin
    et al.
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Ravn, Hans
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Wanhainen, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Regarding "Stent fractures in the Hemobahn/Viabahn stent graft after endovascular popliteal aneurysm repair"2011In: Journal of vascular surgery, ISSN 0741-5214, Vol. 53, no 2, p. 560-560Article in journal (Refereed)
  • 49.
    Björck, Martin
    et al.
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Steuer, Johnny
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Wanhainen, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Delayed abdominal closure for ruptured abdominal aortic aneurysm repair2010In: Italian Journal of Vascular and Endovascular Surgery, ISSN 1824-4777, Vol. 17, no 2, p. 107-115Article in journal (Refereed)
    Abstract [en]

    In this article the pathophysiology and epidemiology of increased intra-abdominal pressure (IAP) and abdominal compartment syndrome (ACS) after repair of ruptured Abdominal Aortic Aneurysms are reviewed. Different methods to measure the IAP are discussed and guidelines how to treat the patient are suggested. In summary, an IAP >20 mmHg (grade III-IV intra-abdominal hypertension, IAH) occurs in approximately 50% of patients treated with open repair (OR), and in 20% after endovascular repair (EVAR), the incidence of ACS is somewhat lower. Patients selected for EVAR are often more hemodynamically stable and have a more favorable anatomy, resulting in less bleeding and consequently a decreased risk of developing IAH/ACS, even if they had been operated on with OR. There is no randomized data. When the pathophysiology is analyzed, the fact that even low grades of IAH have a negative impact on urinary output and respiratory function is highlighted, and early medical therapy is advocated. Medical therapy includes neuromuscular blockade and hypertonic colloid solutions combined with furosemide. This proactive strategy may reduce the number of decompressive laparotomies. An algorithm in how to handle this situation is suggested. When treatment with an open abdomen becomes necessary, it is important to choose a temporary abdominal closure that permits maintaining sterility during prolonged treatment, and that minimizes the risk of fistulation and future abdominal hernia. The suggested method is combining Vacuum-Assisted Wound Closure with mesh-mediated traction, preventing lateralization of the abdominal wall.

  • 50.
    Björck, Martin
    et al.
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Wanhainen, Anders
    Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Vascular Surgery.
    Delayed abdominal closure for ruptured abdominal aortic aneurysm repair2009In: 31st Symposium Book: Vascular and endovascular controversies update / [ed] Roger Malcolm Greenhalgh, London: BIBA Publishing , 2009, p. 214-224Chapter in book (Other academic)
1234567 1 - 50 of 388
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