Literature DB >> 27139899

Atypical hemolytic uremic syndrome: a clinical conundrum.

Prabesh Bajracharya1, Amrish Jain1, Rossana Baracco1, Tej K Mattoo1, Gaurav Kapur2.   

Abstract

BACKGROUND: Patients negative for Shiga toxin-producing E. coli (STEC) are categorized as having atypical hemolytic uremic syndrome (HUS) and are associated with an increased risk for complement mutations and poorer prognosis compared with typical HUS. However, STEC identification is limited by the natural history of HUS.
METHODS: The current study is aimed at identifying HUS patients with poor outcomes based on the presence or absence of diarrhea (D) or Shiga toxin (S). A single-center retrospective review (2003-2012) of 42 HUS patients (follow-up 31.3 ± 38.7 months) was carried out. HUS was managed clinically with supportive treatments such as dialysis, plasma therapy, and eculizumab.
RESULTS: There was no significant difference in the D+S+ (31 %), D+S- (50 %) and D-S- (19 %) groups in the outcome variables of chronic kidney disease stages I-II (100 % vs 81 % vs 67 %) and proteinuria at follow-up (20 % vs 12.5 % vs 33.3 %), hospitalization duration (16.0 ± 8.7 vs 18.1 ± 9.5 vs 23.7 ± 12.9 days); dialysis requirement (50 % vs 81 % vs 66.7 %), and dialysis duration (10.2 ± 1.9 vs 33.3 ± 72.8 vs 10.3 ± 8.1 days). There was no significant difference in study outcomes in STEC+ (59 %) versus STEC- (41 %) groups. Genetic testing was performed in 12 % of HUS patients based on age, recurrent HUS, familial HUS, persistently low C3, or prolonged dialysis, and 80 % of the patients tested were positive for genetic mutations.
CONCLUSIONS: Our study does not show poorer outcomes in STEC- HUS. Indications and the cost-effectiveness of genetic testing, eculizumab, and plasmapheresis in STEC- HUS need to be evaluated further.

Entities:  

Keywords:  Children; HUS; Outcomes; STEC−; aHUS

Mesh:

Substances:

Year:  2016        PMID: 27139899     DOI: 10.1007/s00467-016-3369-6

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


  35 in total

1.  Eculizumab in severe Shiga-toxin-associated HUS.

Authors:  Anne-Laure Lapeyraque; Michal Malina; Véronique Fremeaux-Bacchi; Tobias Boppel; Michael Kirschfink; Mehdi Oualha; François Proulx; Marie-José Clermont; Françoise Le Deist; Patrick Niaudet; Franz Schaefer
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

Review 3.  A classification of hemolytic uremic syndrome and thrombotic thrombocytopenic purpura and related disorders.

Authors:  N Besbas; D Karpman; D Landau; C Loirat; W Proesmans; G Remuzzi; G Rizzoni; C M Taylor; N Van de Kar; L B Zimmerhackl
Journal:  Kidney Int       Date:  2006-06-14       Impact factor: 10.612

4.  Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome.

Authors:  Tara K Maga; Carla J Nishimura; Amy E Weaver; Kathy L Frees; Richard J H Smith
Journal:  Hum Mutat       Date:  2010-06       Impact factor: 4.878

5.  Effect of an oral Shiga toxin-binding agent on diarrhea-associated hemolytic uremic syndrome in children: a randomized controlled trial.

Authors:  Howard Trachtman; Avital Cnaan; Erica Christen; Kathleen Gibbs; Sanyi Zhao; David W K Acheson; Robert Weiss; Frederick J Kaskel; Adrian Spitzer; Gladys H Hirschman
Journal:  JAMA       Date:  2003-09-10       Impact factor: 56.272

6.  Differential impact of complement mutations on clinical characteristics in atypical hemolytic uremic syndrome.

Authors:  Anne-Laure Sellier-Leclerc; Veronique Fremeaux-Bacchi; Marie-Agnès Dragon-Durey; Marie-Alice Macher; Patrick Niaudet; Geneviève Guest; Bernard Boudailliez; François Bouissou; Georges Deschenes; Sophie Gie; Michel Tsimaratos; Michel Fischbach; Denis Morin; Hubert Nivet; Corinne Alberti; Chantal Loirat
Journal:  J Am Soc Nephrol       Date:  2007-06-28       Impact factor: 10.121

7.  Terminal complement inhibitor eculizumab in atypical hemolytic-uremic syndrome.

Authors:  C M Legendre; C Licht; P Muus; L A Greenbaum; S Babu; C Bedrosian; C Bingham; D J Cohen; Y Delmas; K Douglas; F Eitner; T Feldkamp; D Fouque; R R Furman; O Gaber; M Herthelius; M Hourmant; D Karpman; Y Lebranchu; C Mariat; J Menne; B Moulin; J Nürnberger; M Ogawa; G Remuzzi; T Richard; R Sberro-Soussan; B Severino; N S Sheerin; A Trivelli; L B Zimmerhackl; T Goodship; C Loirat
Journal:  N Engl J Med       Date:  2013-06-06       Impact factor: 91.245

8.  Infections in pediatric postdiarrheal hemolytic uremic syndrome: factors associated with identifying shiga toxin-producing Escherichia coli.

Authors:  Rajal K Mody; Ruth E Luna-Gierke; Timothy F Jones; Nicole Comstock; Sharon Hurd; Joni Scheftel; Sarah Lathrop; Glenda Smith; Amanda Palmer; Nancy Strockbine; Deborah Talkington; Barbara E Mahon; Robert M Hoekstra; Patricia M Griffin
Journal:  Arch Pediatr Adolesc Med       Date:  2012-10

9.  Atypical hemolytic uremic syndrome and genetic aberrations in the complement factor H-related 5 gene.

Authors:  Dineke Westra; Katherine A Vernon; Elena B Volokhina; Matthew C Pickering; Nicole C A J van de Kar; Lambert P van den Heuvel
Journal:  J Hum Genet       Date:  2012-05-24       Impact factor: 3.172

10.  Efficacy and safety of eculizumab in atypical hemolytic uremic syndrome from 2-year extensions of phase 2 studies.

Authors:  Christoph Licht; Larry A Greenbaum; Petra Muus; Sunil Babu; Camille L Bedrosian; David J Cohen; Yahsou Delmas; Kenneth Douglas; Richard R Furman; Osama A Gaber; Timothy Goodship; Maria Herthelius; Maryvonne Hourmant; Christophe M Legendre; Giuseppe Remuzzi; Neil Sheerin; Antonella Trivelli; Chantal Loirat
Journal:  Kidney Int       Date:  2015-02-04       Impact factor: 10.612

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  4 in total

1.  Three months interval therapy of Eculizumab in a patient with atypical hemolytic uremic syndrome with hybrid CFHR1/CFH gene.

Authors:  Sami Alobaidi; Ammar AlDabbagh; Amany Alamoudi; Murad Almowarey; Ahmed Akl
Journal:  CEN Case Rep       Date:  2019-02-04

2.  Short- and Long-Term Renal Outcome of Hemolytic-Uremic Syndrome in Childhood.

Authors:  Laura Vaterodt; Johannes Holle; Dieter Hüseman; Dominik Müller; Julia Thumfart
Journal:  Front Pediatr       Date:  2018-08-07       Impact factor: 3.418

3.  Atypical hemolytic uremic syndrome in the Colombian Caribbean: its particular characteristics.

Authors:  Omar Cabarcas-Barbosa; Gustavo Aroca-Martínez; Carlos G Musso; Elizabeth Ramos-Bolaños; Henry González-Tórres; Zilac Espitaleta-Vergara; Alex Domínguez-Vargas; Edufamir Ararat-Rodriguez; José Orozco; Luis Castillo-Parodi; Juan Conde-Manotas; Rodrigo Daza-Arnedo; Víctor Rodríguez-SanJuan; Liliana Gómez-Navarro; Roberto Acosta-Madiedo; Luis Barros-Camargo; Angélica Aduen-Carrillo; Francisco Ayola-Anaya; María Pulgar-Emiliani; Andrés Cadena-Bonfanti
Journal:  Int Urol Nephrol       Date:  2021-10-13       Impact factor: 2.266

4.  Glyco-iELISA: a highly sensitive and unambiguous serological method to diagnose STEC-HUS caused by serotype O157.

Authors:  Kioa L Wijnsma; Susan T Veissi; Sheila A M van Bommel; Rik Heuver; Elena B Volokhina; Diego J Comerci; Juan E Ugalde; Nicole C A J van de Kar; Lambertus P W J van den Heuvel
Journal:  Pediatr Nephrol       Date:  2018-10-26       Impact factor: 3.714

  4 in total

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