ReviewPediatric nephrology (Berlin, Germany)2026
Bloody diarrhea, STEC infection, and HUS in the molecular microbiology era.
Review in Pediatric nephrology (Berlin, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed.
- Serology as an early diagnostic tool in pediatric patients with Shiga toxin-producingJournal of clinical microbiology · 2026Trial
- Risk ranking and antimicrobial resistance of Shiga toxin-producingOne health (Amsterdam, Netherlands) · 2026Article
- A novel multi-epitope mRNA vaccine against Escherichia coli using an in silico reverse vaccinology approach.Journal of applied genetics · 2026Article
- Virulence and Antimicrobial Resistance Traits ofAntibiotics (Basel, Switzerland) · 2026Article
- Global population structure of Shiga toxin-producingMicrobial genomics · 2026Article
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Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Hemolytic uremic syndrome (HUS) associated with Shiga toxin-producing Escherichia coli (STEC) infection remains a major individual and public health challenge throughout the world causing substantial personal, social, and economic burdens. In Western countries, bloody diarrhea (BD) in children is related to STEC infection in at least 6% of cases (rising to 15-20% in summer). This infection may turn into STEC-HUS in about 15% of patients. The widespread use of molecular microbiology leads to the diagnosis of STEC infection before the onset of HUS in an increasing number of patients. The anticipation of the diagnosis creates a window of preventive and/or therapeutic opportunities that include rehydration of dehydrated patients and/or volume expansion that have both proven to mitigate the severity of HUS. Traditionally, antibiotics are not recommended in STEC infections, but recent data suggest a promising potential preventive role for bacteriostatic agents (e.g., azithromycin), if they are given early in the course of the infection. It is recommended to test all children with BD for Shiga toxin (Stx) encoding genes, actively infuse Stx-positive patients with isotonic crystalloid solutions and carefully monitor them with urine dipstick for hemoglobinuria to early identify those who might eventually develop HUS. The suggested approach will increase the detection of STEC-infected patients thus enhancing our knowledge of the mechanisms of disease spreading. The early diagnosis of STEC infection combined with the mentioned therapeutic opportunities will hopefully decrease the number of children suffering from HUS, its case fatality rate and/or improve its short- and long-term outcomes.
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