Literature DB >> 30159625

Outbreak of Shiga toxin-producing Escherichia-coli-associated hemolytic uremic syndrome in Istanbul in 2015: outcome and experience with eculizumab.

Ayşe Ağbaş1, Nilüfer Göknar2, Nurver Akıncı3, Zeynep Yürük Yıldırım4, Mehmet Taşdemir5, Meryem Benzer6, İbrahim Gökçe7, Cengiz Candan8, Nuran Küçük9, Selçuk Uzuner10, Gül Özçelik3, Demet Demirkol11,12, Lale Sever13, Salim Çalışkan13.   

Abstract

BACKGROUND: This study aims to identify epidemiological and clinical characteristics of patients and report our experience with eculizumab treatment during an outbreak of hemolytic uremic syndrome (HUS) caused by Shiga toxin-producing Escherichia coli (STEC) in Istanbul in 2015.
METHODS: Thirty-two children (21 females, median age 3.25 years) were included in this study. Demographic, clinical and laboratory data, and treatment details were retrospectively collected. Renal outcomes were assessed at last follow-up visit. To assess the effect of eculizumab on prognosis of STEC-HUS, subgroup analysis was performed on patients who required dialysis.
RESULTS: A high number of cases occurred within a certain region of Istanbul. Stool samples were cultured from 21 patients (65%), and enteroaggregative E. coli (EAEC; n = 7) and enterohemorrhagic E. coli (EHEC; n = 3) strains were detected. Rates of dialysis treatment, neurological manifestations, and death were 59%, 25%, and 3%, respectively. Mean follow-up duration was 8.6 ± 2.6 months (range 3-12 months). None of the patients (n = 25) was on dialysis at the final visit. The complete renal recovery rate was 54%. Nine patients were treated with eculizumab. At final follow-up visit, no differences in estimated glomerular filtration rate, proteinuria level, or hypertension incidence were observed between patients treated with eculizumab and those not treated with eculizumab.
CONCLUSIONS: An outbreak of EAEC occurred in a specific region of Istanbul. Livestock markets were suspected as the source. Evidence for beneficial effects of eculizumab on renal outcome was not clear in this cohort.

Entities:  

Keywords:  Children; Eculizumab; HUS; Hemolytic uremic syndrome; STEC; Shiga toxin

Mesh:

Substances:

Year:  2018        PMID: 30159625     DOI: 10.1007/s00467-018-4033-0

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN: 0931-041X            Impact factor:   3.714


  32 in total

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Journal:  N Engl J Med       Date:  2011-05-25       Impact factor: 91.245

2.  The United States National Prospective Hemolytic Uremic Syndrome Study: microbiologic, serologic, clinical, and epidemiologic findings.

Authors:  N Banatvala; P M Griffin; K D Greene; T J Barrett; W F Bibb; J H Green; J G Wells
Journal:  J Infect Dis       Date:  2001-03-01       Impact factor: 5.226

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4.  Haemolytic uraemic syndrome and Shiga toxin-producing Escherichia coli infection in children in France. The Société de Néphrologie Pédiatrique.

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Journal:  Epidemiol Infect       Date:  2000-04       Impact factor: 2.451

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Review 6.  Treatment of enterohemorrhagic Escherichia coli-induced hemolytic uremic syndrome (eHUS).

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Journal:  Semin Thromb Hemost       Date:  2014-05-06       Impact factor: 4.180

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9.  Lessons Learned From Outbreaks of Shiga Toxin Producing Escherichia coli.

Authors:  Susanne Hauswaldt; Martin Nitschke; Friedhelm Sayk; Werner Solbach; Johannes K-M Knobloch
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10.  Outbreak of Escherichia coli O104:H4 haemolytic uraemic syndrome in France: outcome with eculizumab.

Authors:  Yahsou Delmas; Benoît Vendrely; Benjamin Clouzeau; Hiba Bachir; Hoang-Nam Bui; Adeline Lacraz; Sébastien Hélou; Cécile Bordes; Armel Reffet; Brigitte Llanas; Sophie Skopinski; Patrick Rolland; Didier Gruson; Christian Combe
Journal:  Nephrol Dial Transplant       Date:  2013-11-28       Impact factor: 5.992

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7.  Therapeutic Strategies to Protect the Central Nervous System against Shiga Toxin from Enterohemorrhagic Escherichia coli.

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