30-Second Takeaway
- Shigella in young children markedly increases risk of prolonged and persistent diarrhoea.
- In hospitalized leptospirosis, age, bilirubin, and pathogen load independently predict death.
Latest - Week ending July 4, 2026
Practical evidence briefs: Shigella morbidity, leptospirosis fatal predictors, TB regimen adoption, PJI outcome heterogeneity, and infection hospitalisation risks in SMI
Shigella is common and prolongs diarrhoea in young children; untreated cases show small growth loss
Among 8756 children aged 6–35 months across seven countries, Shigella was the most commonly attributed pathogen (20.6%). Shigella-attributed diarrhoea was associated with prolonged diarrhoea (≥7 days; aPR 1.56, 95% CI 1.34–1.82) and persistent diarrhoea (≥14 days; aPR 1.66, 95% CI 1.03–2.68). There was no overall association with hospitalization or population-level linear growth faltering, but children with Shigella who did not receive effective antibiotics had greater LAZ/HAZ decline over three months (−0.05, 95% CI −0.09 to −0.01). Pathogen-specific diagnosis and access to effective antibiotics may reduce prolonged illness and modest growth impairment in this age group.
Older age, bilirubin, and leptospiremia predict in-hospital death from leptospirosis
In a multicenter Thai cohort of 459 confirmed leptospirosis cases, 25 patients (5.4%) died during hospitalization. Independent predictors of in-hospital death included older age, higher total bilirubin, and higher leptospiremia measured on admission. A combined clinical plus pathogen-load model showed good discrimination for mortality risk. Genomic data identified Leptospira interrogans clonal lineage predominating among fatal cases, suggesting genomic surveillance may aid public health and risk stratification.
ID clinicians favour short regimens for TB infection but hesitate to adopt new disease regimens
Survey of 349 North American adult ID physicians found 93% prefer ≤4-month regimens for tuberculosis infection. Uptake of newer regimens for TB disease was low; only 1% had used HPMZ for drug-susceptible disease and 5% reported experience with HPMZ. Many clinicians were uncertain about effectiveness of 4- and 6-month disease regimens (≈43% uncertain; 40% unsure about regimen choice for resistant disease). Respondents cited concerns about toxicities, drug interactions, and drug availability as primary barriers to adoption.
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Additional Reads
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