Validation of treatment strategies for enterohaemorrhagic Escherichia coli O104:H4 induced haemolytic uraemic syndrome: case-control study.
case_control · Level III
Where this comes from
- Record sourced from PubMed, PMID 22815429.
- Also identified by DOI 10.1136/bmj.e4565 and PMC identifier 3400392.
- Licence recorded as CC BY-NC.
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Abstract
To evaluate the effect of different treatment strategies on enterohaemorrhagic Escherichia coli O104:H4 induced haemolytic uraemic syndrome. Multicentre retrospective case-control study. 23 hospitals in northern Germany. 298 adults with enterohaemorrhagic E coli induced haemolytic uraemic syndrome. Dialysis, seizures, mechanical ventilation, abdominal surgery owing to perforation of the bowel or bowel necrosis, and death. 160 of the 298 patients (54%) temporarily required dialysis, with only three needing treatment long term. 37 patients (12%) had seizures, 54 (18%) required mechanical ventilation, and 12 (4%) died. No clear benefit was found from use of plasmapheresis or plasmapheresis with glucocorticoids. 67 of the patients were treated with eculizumab, a monoclonal antibody directed against the complement cascade. No short term benefit was detected that could be attributed to this treatment. 52 patients in one centre that used a strategy of aggressive treatment with combined antibiotics had fewer seizures (2% v 15%, P = 0.03), fewer deaths (0% v 5%, p = 0.029), required no abdominal surgery, and excreted E coli for a shorter duration. Enterohaemorrhagic E coli induced haemolytic uraemic syndrome is a severe self limiting acute condition. Our findings question the benefit of eculizumab and of plasmapheresis with or without glucocorticoids. Patients with established haemolytic uraemic syndrome seemed to benefit from antibiotic treatment and this should be investigated in a controlled trial.
Medical subject headings
- Anti-Bacterial Agents
- Antibodies, Monoclonal, Humanized
- Disease Outbreaks
- Enterohemorrhagic Escherichia coli
- Escherichia coli Infections
- Hemolytic-Uremic Syndrome
- Immunologic Factors