Evidence map›Paper›PMID 41966655›Full record

ArticleRheumatology and therapy2026

Frequency and Impact of Serious Infections in Hospitalised Patients with Sjögren's Disease: A Longitudinal Cohort Study.

Johannes C Nossent, Charles A Inderjeeth

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Article in Rheumatology and therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Johannes C NossentRheumatology Group, Medical School, University of Western Australia, 35 Stirling Highway (M503), Perth, WA, Australia. johannes.nossent@uwa.edu.au.ORCID http://orcid.org/0000-0002-2833-7997
Charles A InderjeethRheumatology Group, Medical School, University of Western Australia, 35 Stirling Highway (M503), Perth, WA, Australia.ORCID http://orcid.org/0000-0003-0535-963X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAs little is known about the risk, type and severity of infections in patients with Sjögren's disease (SjD), we compared the frequency and impact of serious infections (SI) between hospitalised patients with SjD and controls (Co).

methodsPopulation-level observational study of patients with SjD (n = 692, 87.9% female, age 67 years) identified in the Hospital Morbidity Data Collection (HDMC) in Western Australia (WA) between 1980 and 2015 by diagnostic codes (ICD-9 CM 710.2, ICD10-AM M35.0) and age- and gender-matched controls free of rheumatic disease (n = 3737, 87.5% female, age 67 years). SI were defined by a validated algorithm and primary SjD, as the absence of other autoimmune rheumatic disease. Odds ratios (OR), incidence rates (IR) per 100 person-years (PY) and IR ratios (IRR) with 95% CI for SI were estimated. HDMC data were linked to WA Death Registry to evaluate the impact of SI on mortality rates (MR) per 100 PY and Kaplan-Meier survival estimates.

resultsSerious infections occurred more in patients with SjD (OR 1.87, CI 1.59, 2.21, p < 0.01) with a fourfold higher IR for SI (IRR 4.28, CI 4.02-4.56) and increased IRR for pneumonia (4.01, CI 3.50-4.60), urogenital (3.06, CI 2.73-3.43), skin/soft tissue (5.22, CI 4.60-5.90), opportunistic infections (6.93, CI 5.77-8.32) and sepsis (6.15, CI 4.87-7.74) (all p < 0.01). The MR for patients with SjD with SI was almost twice that for Co with SI (MR ratio 1.89, CI 1.65-2.16). Patients with associated SjD (n = 270, 39%) had increased OR (2.05, CI 1.49-2.82) and IRR (1.61, CI 1.44-1.79) for SI compared to patients with primary SjD (n = 422, 61%). Few differences in SI existed between patients with SjD associated with rheumatoid arthritis (n = 197) or SLE (n = 79).

conclusionsSI occurred at a higher rate in all patients with SjD and was associated with increased long-term mortality. These results emphasize the increased susceptibility to and impact of SI for both patients with primary and secondary SjD.

Indexed as

IncidenceSerious infectionsSjögren’s diseaseStandardised mortalitySurvival

Identifiers

PMID41966655
PMCPMC13198561

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