Targeted caspofungin prophylaxis for invasive aspergillosis in high-risk liver transplant recipients, a single-center experience.


Journal

Transplant infectious disease : an official journal of the Transplantation Society
ISSN: 1399-3062
Titre abrégé: Transpl Infect Dis
Pays: Denmark
ID NLM: 100883688

Informations de publication

Date de publication:
Aug 2021
Historique:
revised: 04 11 2020
received: 06 09 2020
accepted: 03 01 2021
pubmed: 16 1 2021
medline: 23 9 2021
entrez: 15 1 2021
Statut: ppublish

Résumé

Invasive aspergillosis (IA) is a rare but highly lethal complication after orthotopic liver transplantation (OLT). Targeted antifungal prophylaxis has been proposed as a strategy to prevent IA among orthotopic liver transplant recipient (OLTr), but limited data are available to support its efficacy. We conducted a single-center, retrospective, before and after cohort study, comparing IA incidences among OLTr who did not receive antifungal prophylaxis after transplantation (cohort 1) to OLTr who received targeted antifungal prophylaxis after liver transplantation (cohort 2). Patients in cohort 2 received caspofungin prophylaxis if they presented one of the following risk factors: retransplantation, acute liver failure, dialysis, or Aspergillus colonization prior to transplantation. The primary outcome was IA at 90 days after transplantation. A total of 391 OLTr were included in the study; 181 patients in the cohort 1 (no prophylaxis) and 210 patients in the cohort 2 (targeted prophylaxis). Among patients in cohort 2, 19% (40/ 210) were considered at high risk for IA and 85% (34/40) of those received caspofungin prophylaxis. The incidence of IA at 90 days was 3.3% (6/ 181) and 0.5% (1/ 210), in cohort 1 and 2, respectively (OR 0.14; 95%CI 0.01-0.83; P = .03). Ninety-day mortality was similar among the two cohorts (3.9% (7/181) and 2.4% (5/210) in cohort 1 and 2, respectively (OR 0.61; 95% 0.18-1.93; P = .40)). The 90-day mortality among the OLTs with IA was 71% (5/7). Targeted caspofungin prophylaxis was associated with lower rate of IA.

Sections du résumé

BACKGROUND BACKGROUND
Invasive aspergillosis (IA) is a rare but highly lethal complication after orthotopic liver transplantation (OLT). Targeted antifungal prophylaxis has been proposed as a strategy to prevent IA among orthotopic liver transplant recipient (OLTr), but limited data are available to support its efficacy.
METHOD METHODS
We conducted a single-center, retrospective, before and after cohort study, comparing IA incidences among OLTr who did not receive antifungal prophylaxis after transplantation (cohort 1) to OLTr who received targeted antifungal prophylaxis after liver transplantation (cohort 2). Patients in cohort 2 received caspofungin prophylaxis if they presented one of the following risk factors: retransplantation, acute liver failure, dialysis, or Aspergillus colonization prior to transplantation. The primary outcome was IA at 90 days after transplantation.
RESULTS RESULTS
A total of 391 OLTr were included in the study; 181 patients in the cohort 1 (no prophylaxis) and 210 patients in the cohort 2 (targeted prophylaxis). Among patients in cohort 2, 19% (40/ 210) were considered at high risk for IA and 85% (34/40) of those received caspofungin prophylaxis. The incidence of IA at 90 days was 3.3% (6/ 181) and 0.5% (1/ 210), in cohort 1 and 2, respectively (OR 0.14; 95%CI 0.01-0.83; P = .03). Ninety-day mortality was similar among the two cohorts (3.9% (7/181) and 2.4% (5/210) in cohort 1 and 2, respectively (OR 0.61; 95% 0.18-1.93; P = .40)). The 90-day mortality among the OLTs with IA was 71% (5/7).
CONCLUSION CONCLUSIONS
Targeted caspofungin prophylaxis was associated with lower rate of IA.

Identifiants

pubmed: 33450126
doi: 10.1111/tid.13568
doi:

Substances chimiques

Caspofungin F0XDI6ZL63

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e13568

Informations de copyright

© 2021 Wiley Periodicals LLC.

Références

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Auteurs

Arpita Chakravarti (A)

Division of Infectious Disease, Department of Medicine, University of Montreal Hospital Center, Montreal, QC, Canada.

Guillaume Butler-Laporte (G)

Division of Infectious Disease, Department of Medicine, McGill University Health Center, Montreal, QC, Canada.

Francois Martin Carrier (FM)

Department of Anesthesiology, University of Montreal Hospital Center, Montreal, QC, Canada.
Division of Critical Care, Department of Medicine, University of Montreal Hospital Center, Montreal, QC, Canada.

Marc Bilodeau (M)

Division of Hepatology, Department of Medicine, University of Montreal Hospital Center, Montreal, QC, Canada.

Genevieve Huard (G)

Division of Hepatology, Department of Medicine, University of Montreal Hospital Center, Montreal, QC, Canada.

Daniel Corsilli (D)

Division of Critical Care, Department of Medicine, University of Montreal Hospital Center, Montreal, QC, Canada.
Division of Hepatology, Department of Medicine, University of Montreal Hospital Center, Montreal, QC, Canada.

Patrice Savard (P)

Division of Infectious Disease, Department of Medicine, University of Montreal Hospital Center, Montreal, QC, Canada.

Me-Linh Luong (ML)

Division of Infectious Disease, Department of Medicine, University of Montreal Hospital Center, Montreal, QC, Canada.

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