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Integrating Multimorbidity Assessment into Rheumatology Care: Prognostic Role of the Charlson Comorbidity Index in
Ryuichi Ohta1, Yoshinori Ryu1, Chiaki Sano2
1Department of Community Care, Unnan City Hospital, Unnan 699-1221, Japan.
Insights
The Charlson Comorbidity Index (CCI) strongly predicts mortality in systemic lupus erythematosus (SLE) patients. Higher CCI scores indicate a greater burden of comorbid conditions and increased risk of death, highlighting its prognostic value.
Area of Science:
- Rheumatology
- Internal Medicine
- Epidemiology
Background:
- Systemic lupus erythematosus (SLE) is a chronic autoimmune disease associated with significant morbidity and premature mortality.
- Patients with SLE frequently experience multiple comorbid conditions, necessitating comprehensive health burden assessment for improved risk stratification and outcomes.
- The Charlson Comorbidity Index (CCI) is a validated tool for quantifying comorbidity burden.
Purpose of the Study:
- To systematically review and meta-analyze the prognostic value of the CCI for all-cause mortality in adult patients with SLE.
- To assess the association between comorbidity burden, as measured by CCI, and mortality risk in SLE.
Main Methods:
- Systematic review and meta-analysis conducted following PRISMA 2020 guidelines.
- Searched PubMed, Embase, and Web of Science databases up to May 2025.
- Included three observational studies (n=1175) evaluating CCI and all-cause mortality in adult SLE patients; pooled odds ratios (ORs) calculated using a fixed-effects model; risk of bias assessed with Newcastle-Ottawa Scale.
Main Results:
- Three studies (n=1175) met inclusion criteria, all showing a significant link between higher CCI scores and increased all-cause mortality.
- The pooled OR for mortality in patients with high comorbidity burden was 3.92 (95% CI: 2.74-5.60), with no heterogeneity observed (I²=0%).
- Risk of bias was assessed as moderate to high across the included studies.
Conclusions:
- Multimorbidity, quantified by the CCI, serves as a robust independent predictor of mortality in SLE.
- Integrating CCI assessment into rheumatology care can enhance prognostic evaluation and guide personalized treatment strategies.
- This approach supports interdisciplinary management for SLE patients with complex health profiles.
Abstract:
Background/Objectives: Systemic lupus erythematosus (SLE) is a chronic autoimmune disease with significant morbidity and premature mortality. As patients with SLE often suffer from multiple comorbid conditions, evaluating the overall health burden is critical for improving risk stratification and long-term outcomes. The Charlson Comorbidity Index (CCI) is a widely used tool for quantifying the burden of comorbidity. This systematic review and meta-analysis aimed to assess the prognostic value of the CCI for all-cause mortality in adult patients with SLE. Methods: We conducted a systematic review and meta-analysis in accordance with the PRISMA 2020 guidelines. Three databases (PubMed, Embase, and Web of Science) were searched up to May 2025. Three studies (n = 1175 participants) met the inclusion criteria. Eligible studies included adult SLE populations that evaluated the comorbidity burden using the CCI and reported all-cause mortality. Study characteristics and effect sizes were extracted, and a fixed-effects model (after considering both random- and fixed-effects approaches) was applied to calculate pooled odds ratios (ORs). Risk of bias was assessed using the Newcastle-Ottawa Scale. Results: Three observational studies (n = 1175 participants) met the inclusion criteria. All demonstrated a significant association between higher CCI scores and increased all-cause mortality. The pooled OR for mortality in patients with a high comorbidity burden was 3.92 (95% CI: 2.74-5.60), with no observed heterogeneity (I2 = 0%). The risk of bias was moderate to high across all studies. Conclusions: Multimorbidity, as measured by the CCI, is a strong independent predictor of mortality in SLE. Integrating comorbidity assessment into rheumatology care may enhance prognostic evaluation, guide personalized treatment, and support interdisciplinary management strategies for patients with complex disease profiles.
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