Literature DB >> 23660733

Clinical features of critically ill patients with Shiga toxin-induced hemolytic uremic syndrome.

Stephan A Braune1, Dominic Wichmann, Marie C von Heinz, Axel Nierhaus, Heinrich Becker, Tobias N Meyer, Gerd P Meyer, Matthias Müller-Schulz, Jens Fricke, Andreas de Weerth, Wilhelm-W Hoepker, Jens Fiehler, Tim Magnus, Christian Gerloff, Ulf Panzer, Rolf A K Stahl, Karl Wegscheider, Stefan Kluge.   

Abstract

OBJECTIVE: In Spring 2011, an unprecedented outbreak of Shiga toxin-producing Escherichia coli serotype O104:H4-associated hemolytic uremic syndrome occurred in Northern Germany. The aim of this study was to describe the clinical characteristics, treatments, and outcomes of critically ill patients with Shiga toxin-producing E. coli-associated hemolytic uremic syndrome during this outbreak. DESIGN, SETTING, AND PATIENTS: Multicenter, retrospective, observational study of critically ill adult patients with Shiga toxin-producing E. coli-associated hemolytic uremic syndrome in six hospitals in Hamburg, Germany, between May 2011 and August 2011.
MEASUREMENTS AND MAIN RESULTS: During the study period, 106 patients with Shiga toxin-producing E. coli-associated hemolytic uremic syndrome were admitted to eight ICUs. The median age was 40 years (range, 18-83) with a female:male ratio of 3:1. The median time from onset of clinical symptoms to hospital admission was 3 days and from hospital to ICU admission an additional 3 days. A total of 101 patients (95.3%) had acute renal failure and 78 (73.6%) required renal replacement therapy. Intubation and mechanical ventilation were required in 38 patients (35.8%) and noninvasive ventilation was required in 17 patients (16.0%). The median duration of invasive ventilation was 7 days (range, 1-32 days) and the median ICU stay was 10 days (range, 1-45 days). Fifty-one patients (48.1%) developed sepsis; of these 51 patients, 27 (25.4%) developed septic shock. Seventy patients (66.0%) developed severe neurological symptoms. Ninety-seven patients (91.5%) were treated with plasma exchange and 50 patients (47.2%) received eculizumab (monoclonal anti-C5 antibody). The mortality rate was 4.7%. Mild residual neurological symptoms were present in 21.7% of patients at ICU discharge, and no patient required renal replacement therapy 6 months after ICU admission.
CONCLUSIONS: During the 2011 Shiga toxin-producing E. coli-associated hemolytic uremic syndrome outbreak in Germany, critical illness developed rapidly after hospital admission, often in young women. The infection was associated with severe neurological and renal symptoms, requiring mechanical ventilation and renal replacement therapy in a substantial proportion of patients. Overall, recovery was much better than expected.

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Year:  2013        PMID: 23660733     DOI: 10.1097/CCM.0b013e31828a24a8

Source DB:  PubMed          Journal:  Crit Care Med        ISSN: 0090-3493            Impact factor:   7.598


  11 in total

1.  CFH gene mutation in a case of Shiga toxin-associated hemolytic uremic syndrome (STEC-HUS).

Authors:  Caroline Caillaud; Ariane Zaloszyc; Christoph Licht; Valérie Pichault; Véronique Frémeaux-Bacchi; Michel Fischbach
Journal:  Pediatr Nephrol       Date:  2015-09-23       Impact factor: 3.714

2.  What's new in the diagnosis and pathophysiology of thrombotic thrombocytopenic purpura.

Authors:  J Evan Sadler
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2015

Review 3.  Shiga Toxin-Associated Hemolytic Uremic Syndrome: Specificities of Adult Patients and Implications for Critical Care Management.

Authors:  Benoit Travert; Cédric Rafat; Patricia Mariani; Aurélie Cointe; Antoine Dossier; Paul Coppo; Adrien Joseph
Journal:  Toxins (Basel)       Date:  2021-04-26       Impact factor: 4.546

4.  Ketamine and propofol combination ("ketofol") for endotracheal intubations in critically ill patients: a case series.

Authors:  Alice Gallo de Moraes; Carlos J Racedo Africano; Sumedh S Hoskote; Dereddi Raja S Reddy; Rudy Tedja; Lokendra Thakur; Jasleen K Pannu; Elizabeth C Hassebroek; Nathan J Smischney
Journal:  Am J Case Rep       Date:  2015-02-13

5.  Cerebral Hemodynamics in Patients with Hemolytic Uremic Syndrome Assessed by Susceptibility Weighted Imaging and Four-Dimensional Non-Contrast MR Angiography.

Authors:  Ulrike Löbel; Nils Daniel Forkert; Peter Schmitt; Thorsten Dohrmann; Maria Schroeder; Tim Magnus; Stefan Kluge; Christina Weiler-Normann; Xiaoming Bi; Jens Fiehler; Jan Sedlacik
Journal:  PLoS One       Date:  2016-11-01       Impact factor: 3.240

Review 6.  Public Health Research Resulting from One of the World's Largest Outbreaks Caused by Entero-Hemorrhagic Escherichia coli in Germany 2011: A Review.

Authors:  Elena Köckerling; Laura Karrasch; Aparna Schweitzer; Oliver Razum; Gérard Krause
Journal:  Front Public Health       Date:  2017-12-11

Review 7.  [Intensive care back up for infectious disease disasters].

Authors:  D Wichmann; H Matthews; M F Nentwich; S Schmiedel; S Kluge
Journal:  Med Klin Intensivmed Notfmed       Date:  2020-10-09       Impact factor: 0.840

8.  Severely ill pediatric patients with Shiga toxin-associated hemolytic uremic syndrome (STEC-HUS) who suffered from multiple organ involvement in the early stage.

Authors:  Mariana Luna; Mariana Kamariski; Iliana Principi; Victoria Bocanegra; Patricia G Vallés
Journal:  Pediatr Nephrol       Date:  2020-11-17       Impact factor: 3.714

Review 9.  Ribosomal alteration-derived signals for cytokine induction in mucosal and systemic inflammation: noncanonical pathways by ribosomal inactivation.

Authors:  Yuseok Moon
Journal:  Mediators Inflamm       Date:  2014-01-02       Impact factor: 4.711

Review 10.  Shiga Toxin-Associated Hemolytic Uremic Syndrome: A Narrative Review.

Authors:  Adrien Joseph; Aurélie Cointe; Patricia Mariani Kurkdjian; Cédric Rafat; Alexandre Hertig
Journal:  Toxins (Basel)       Date:  2020-01-21       Impact factor: 4.546

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