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Systematic review and meta-analysis of sepsis screening tools in low- and middle-income countries

Systematic review and meta-analysis of sepsis screening tools in low- and middle-income countries
Photo by Joshua Chehov / Unsplash
Key Takeaway
Consider that no single sepsis screening tool shows optimal performance in low- and middle-income countries.

This is a systematic review and meta-analysis of sepsis screening tools in adult populations within low- and middle-income countries (LMICs). The review synthesized data from 30,310 patients to compare the diagnostic accuracy of tools including qSOFA, NEWS, MEWS, UVA, SIRS, and SOFA.

Key findings show qSOFA had a sensitivity of 0.51 (95% CI: 0.42–0.60) and specificity of 0.83 (95% CI: 0.77–0.88), with an AUROC of 0.74. SIRS had higher sensitivity (0.86) but lower specificity (0.32). NEWS AUROC was 0.77 (95% CI: 0.73–0.81), SOFA AUROC was 0.75 (95% CI: 0.71–0.79), and UVA AUROC was 0.74 (95% CI: 0.70–0.78). qSOFA had a positive likelihood ratio of 3.00 and a negative likelihood ratio of 0.59.

The authors note substantial heterogeneity across studies (I2 > 75%) and that confidence intervals overlapped substantially across tools. They highlight the limited rule-out capacity of qSOFA. No single tool demonstrated optimal performance across all metrics.

Practice relevance suggests tool selection should be guided by local healthcare priorities and available laboratory capacity, with tiered screening strategies potentially optimizing sepsis recognition. The review does not report follow-up duration, safety data, or funding disclosures.

Study Details

Study typeMeta analysis
EvidenceLevel 1
PublishedMay 2026
View Original Abstract ↓
BackgroundSepsis causes disproportionate mortality in low- and middle-income countries (LMICs), yet evidence on screening tool performance in these resource-limited settings remains fragmented.ObjectiveThis systematic review and meta-analysis aimed to evaluate and compare the diagnostic accuracy of sepsis screening tools—ranging from purely clinical assessments (qSOFA, NEWS, MEWS, UVA) to those incorporating laboratory parameters (SIRS, SOFA)—for sepsis identification in adult populations within LMICs.MethodsA comprehensive search of PubMed, Embase, Cochrane Library, Web of Science, and Global Index Medicus was conducted from inception through June 2025. Eligible studies evaluated sepsis screening tools ranging from purely clinical bedside assessments (qSOFA, NEWS, MEWS, UVA) to those requiring basic laboratory parameters (SIRS, SOFA), enabling comparison across the resource-availability spectrum in LMICs. Bivariate random-effects models were employed to calculate pooled sensitivity, specificity, and area under the hierarchical summary receiver operating characteristic curve (AUROC). Evidence quality was assessed using the GRADE approach.ResultsTwenty-seven studies encompassing 30,310 patients across 14 LMICs were included. qSOFA demonstrated pooled sensitivity of 0.51 (95% CI: 0.42–0.60) and specificity of 0.83 (95% CI: 0.77–0.88) with AUROC of 0.74. SIRS exhibited high sensitivity (0.86) but poor specificity (0.32). NEWS achieved the highest point estimate of discriminative ability (AUROC 0.77, 95% CI: 0.73–0.81), followed by SOFA (AUROC 0.75, 95% CI: 0.71–0.79) and UVA (AUROC 0.74, 95% CI: 0.70–0.78), although confidence intervals overlapped substantially across tools. qSOFA yielded a positive likelihood ratio (LR+) of 3.00 and a negative likelihood ratio (LR−) of 0.59, indicating moderate rule-in but limited rule-out utility. Substantial heterogeneity was observed across studies (I2 > 75%).ConclusionNo single screening tool demonstrates optimal performance across all metrics in LMIC populations. When analysis is restricted to purely clinical tools requiring no laboratory parameters, NEWS (AUROC 0.77) and qSOFA (AUROC 0.74) demonstrate comparable discriminative ability with broadly overlapping confidence intervals, supporting their consideration in the most resource-constrained settings. However, the limited rule-out capacity of qSOFA (LR − 0.59) suggests it should not be used as a standalone screening tool. Tool selection should be guided by local healthcare priorities and available laboratory capacity, with tiered screening strategies potentially optimizing sepsis recognition while ensuring efficient resource allocation.
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