Fifteen-year, single-center experience with in situ reconstruction for infected native aortic aneurysms.


Journal

Journal of vascular surgery
ISSN: 1097-6809
Titre abrégé: J Vasc Surg
Pays: United States
ID NLM: 8407742

Informations de publication

Date de publication:
03 2022
Historique:
received: 12 05 2021
accepted: 24 08 2021
pubmed: 3 10 2021
medline: 8 3 2022
entrez: 2 10 2021
Statut: ppublish

Résumé

The purpose of the present study was to evaluate the survival and freedom from reinfection for patients with infected native aortic aneurysms (INAAs) treated with in situ revascularization (ISR), using either open surgical repair (OSR) or endovascular aneurysm repair (EVAR), and to identify the predictors of outcome. Patients with INAAs who had undergone ISR from January 2005 to December 2020 were included in the present retrospective single-center study. The diagnosis of INAAs required a combination of two or more of the following criteria: (1) clinical presentation, (2) laboratory results, (3) imaging findings, and (4) intraoperative findings. The primary endpoint was 30-day mortality. The secondary endpoints were in-hospital mortality, estimated survival, patency, and freedom from reinfection using the Kaplan-Meier method. The predictive factors for adverse outcomes were evaluated using the Mann-Whitney U test or the Fisher exact test and multivariate regression analysis. A total of 65 patients (53 men [81.5%]; median age, 69.0 years; interquartile range, 61.5-75.0 years) were included, 31 (47.7%) were immunocompromised, 60 were symptomatic (92.3%), and 32 (49.2%) had presented with rupture, including 3 aortocaval fistulas (4.6%) and 12 aortoenteric fistulas (18.5%). The most common location was infrarenal (n = 39; 60.0%). Of the 65 patients, 55 (84.6%) had undergone primary OSR with ISR, 3 (4.6%) had required EVAR as a bridge to OSR, and 8 (12.3%) had undergone EVAR as definitive treatment. The approach was a midline laparotomy for 44 patients (67.7%), mostly followed by reconstruction and aortic-aortic bypass (n = 28; 40.6%) and the use of a silver and triclosan Dacron graft (n = 30; 43.5%). Causative organisms were identified in 55 patients (84.6%). The 30-day and in-hospital mortality rates were 6.2% (n = 4) and 10.8% (n = 7). The median follow-up was 33.5 months (interquartile range, 13.6-62.3 months). The estimated 1- and 5-year survival rates were 79.7% (95% confidence interval [CI], 67.6%-87.7%) and 67.4% (95% CI, 51.2%-79.3%). The corresponding freedom from reinfection rates were 92.5% (95% CI, 81.1%-97.1%) and 79.4% (95% CI, 59.1%-90.3%). On multivariate analysis, in-hospital mortality increased with uncontrolled sepsis (P < .0001), rapidly expanding aneurysms (P = .008), and fusiform aneurysms (P = .03). The incidence of reinfection increased with longer operating times (P = .009). The selective use of ISR and OSR combined with targeted antimicrobial therapy functioned reasonably well in the treatment of INAAs, although larger, prospective, multicenter studies with appropriately powered comparative cohorts are necessary to confirm our findings and to determine the best vascular substitute and precise role of EVAR as a bridge to OSR or definitive treatment.

Identifiants

pubmed: 34600030
pii: S0741-5214(21)02159-5
doi: 10.1016/j.jvs.2021.08.094
pii:
doi:

Substances chimiques

Anti-Bacterial Agents 0

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

950-961.e5

Informations de copyright

Copyright © 2021 Society for Vascular Surgery. Published by Elsevier Inc. All rights reserved.

Auteurs

Xavier Berard (X)

Department of Vascular Surgery, Bordeaux University Hospital, Bordeaux, France. Electronic address: xavier.berard@chu-bordeaux.fr.

Anne-Sophie Battut (AS)

Department of Vascular Surgery, Bordeaux University Hospital, Bordeaux, France.

Mathilde Puges (M)

Department of Infectious Diseases, Bordeaux University Hospital, Bordeaux, France.

Mathilde Carrer (M)

Department of Infectious Diseases, Bordeaux University Hospital, Bordeaux, France.

Katherine Stenson (K)

Department of Vascular Surgery, Imperial College London, London, UK.

Charles Cazanave (C)

Department of Infectious Diseases, Bordeaux University Hospital, Bordeaux, France.

Laurent Stecken (L)

Department of Anesthesiology, Bordeaux University Hospital, Bordeaux, France.

Caroline Caradu (C)

Department of Vascular Surgery, Bordeaux University Hospital, Bordeaux, France.

Eric Ducasse (E)

Department of Vascular Surgery, Bordeaux University Hospital, Bordeaux, France.

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