» Articles » PMID: 16148732

Deaths Occurring During the First Year After Treatment Onset for Polyarteritis Nodosa, Microscopic Polyangiitis, and Churg-Strauss Syndrome: a Retrospective Analysis of Causes and Factors Predictive of Mortality Based on 595 Patients

Overview
Specialty General Medicine
Date 2005 Sep 9
PMID 16148732
Citations 54
Authors
Affiliations
Soon will be listed here.
Abstract

Although combining corticosteroids and cyclophosphamide has greatly improved the prognoses of severe necrotizing vasculitides, some patients continue to have fulminating disease and die within the first year of diagnosis. To evaluate the characteristics of these patients, we retrospectively studied the files of 60 patients who died within the first year (20 patients with hepatitis B virus-associated polyarteritis nodosa [HBV-PAN], 18 with non-HBV PAN, 13 with microscopic polyangiitis [MPA], and 9 with Churg-Strauss syndrome [CSS]) and 535 first-year survivors (89 patients with HBV-PAN, 182 with non-HBV PAN, 140 with MPA, and 124 with CSS), 85 of whom died during a mean follow-up of 6.4 years. The 2 groups were compared for prognostic factors defined by the five-factor score (FFS) and Birmingham Vasculitis Activity Score at baseline, clinical signs, treatment, outcome, and causes of death. For first-year nonsurvivors, the clinical signs predictive of death were as follows: renal involvement (hazard ratio [HR], 1.6; 95% confidence intervals [CI], 1.09-2.3) or central nervous system involvement (HR, 2.3; 95% CI, 1.5-3.7), and a trend toward cardiomyopathy (HR, 1.4; 95% CI, 1.000-2.115). Older patients died earlier (HR, 1.04; 95% CI, 1.023-1.051). Gastrointestinal symptoms were most frequently associated with early death from HBV-PAN, while 83% of CSS patients died of cardiac involvement. Treatment had no significant impact on early death, except for patients with FFS > or = 2, for whom steroids alone were associated (p < 0.05). The major cause of early death was uncontrolled vasculitis (58%), followed by infection (26%). Cyclophosphamide-induced cytopenia and infection were responsible for 2 deaths. Despite these iatrogenic complications, early deaths were more frequently the consequence of insufficient or inappropriate therapy.

Citing Articles

Proteinase‑3‑antineutrophil cytoplasmic antibody‑associated vasculitis secondary to subacute infective endocarditis: A case report.

Lu H, Cui Z, Zhou X, Yang Y, Han X, Li X Exp Ther Med. 2024; 27(5):216.

PMID: 38590565 PMC: 11000458. DOI: 10.3892/etm.2024.12504.


Risk prediction model for mortality in microscopic polyangiitis: multicentre REVEAL cohort study.

Kotani T, Matsuda S, Okazaki A, Nishioka D, Watanabe R, Gon T Arthritis Res Ther. 2023; 25(1):223.

PMID: 37986108 PMC: 10658814. DOI: 10.1186/s13075-023-03210-8.


Renal involvement in eosinophilic granulomatosis with polyangiitis.

Reggiani F, LImperio V, Calatroni M, Pagni F, Sinico R Front Med (Lausanne). 2023; 10:1244651.

PMID: 37790127 PMC: 10544898. DOI: 10.3389/fmed.2023.1244651.


Recovery and long-term renal outcome of patients with anti-neutrophil cytoplasmic antibody-associated vasculitis who are on dialysis at presentation.

Lee Y, Ahn S, Oh J, Kim Y, Lee C, Yoo B J Rheum Dis. 2023; 30(4):251-259.

PMID: 37736589 PMC: 10509644. DOI: 10.4078/jrd.2023.0031.


Mepolizumab exerts crucial effects on glucocorticoid discontinuation in patients with eosinophilic granulomatosis with polyangiitis: a retrospective study of 27 cases at a single center in Japan.

Yamane T, Hashiramoto A Arthritis Res Ther. 2023; 25(1):110.

PMID: 37365612 PMC: 10291743. DOI: 10.1186/s13075-023-03097-5.