Patients with ANCA-associated vasculitis admitted to the intensive care unit with acute vasculitis manifestations: a retrospective and comparative multicentric study.

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Version: Final published version
Serval ID
serval:BIB_9AD3A2C15EBE
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Patients with ANCA-associated vasculitis admitted to the intensive care unit with acute vasculitis manifestations: a retrospective and comparative multicentric study.
Journal
Annals of intensive care
Author(s)
Demiselle J., Auchabie J., Beloncle F., Gatault P., Grangé S., Du Cheyron D., Dellamonica J., Boyer S., Beauport D.T., Piquilloud L., Letheulle J., Guitton C., Chudeau N., Geri G., Fourrier F., Robert R., Guérot E., Boisramé-Helms J., Galichon P., Dequin P.F., Lautrette A., Bollaert P.E., Meziani F., Guillevin L., Lerolle N., Augusto J.F.
ISSN-L
2110-5820
Publication state
Published
Issued date
12/2017
Peer-reviewed
Oui
Volume
7
Number
1
Pages
39
Language
english
Notes
Publication types: Journal Article
Publication Status: ppublish
Abstract
Data for ANCA-associated vasculitis (AAV) patients requiring intensive care are scarce.
We included 97 consecutive patients with acute AAV manifestations (new onset or relapsing disease), admitted to 18 intensive care units (ICUs) over a 10-year period (2002-2012). A group of 95 consecutive AAV patients with new onset or relapsing disease, admitted to two nephrology departments with acute vasculitis manifestations, constituted the control group.
In the ICU group, patients predominantly showed granulomatosis with polyangiitis and proteinase-3 ANCAs. Compared with the non-ICU group, the ICU group showed comparable Birmingham vasculitis activity score and a higher frequency of heart, central nervous system and lungs involvements. Respiratory assistance, renal replacement therapy and vasopressors were required in 68.0, 56.7 and 26.8% of ICU patients, respectively. All but one patient (99%) received glucocorticoids, 85.6% received cyclophosphamide, and 49.5% had plasma exchanges as remission induction regimens. Fifteen (15.5%) patients died during the ICU stay. The following were significantly associated with ICU mortality in the univariate analysis: the need for respiratory assistance, the use of vasopressors, the occurrence of at least one infection event in ICU, cyclophosphamide treatment, sequential organ failure assessment at admission and simplified acute physiology score II. After adjustment on sequential organ failure assessment or infection, cyclophosphamide was no longer a risk factor for mortality. Despite a higher initial mortality rate of ICU patients within the first hospital stay (p < 0.0001), the long-term mortality of hospital survivors did not differ between ICU and non-ICU groups (18.6 and 20.4%, respectively, p = 0.36). Moreover, we observed no renal survival difference between groups after a 1-year follow-up (82.1 and 80.5%, p = 0.94).
This study supports the idea that experiencing an ICU challenge does not impact the long-term prognosis of AAV patients.

Pubmed
Web of science
Open Access
Yes
Create date
25/04/2017 18:22
Last modification date
20/08/2019 16:01
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