Literature DB >> 27646857

First-Line, Early and Long-Term Eculizumab Therapy in Atypical Hemolytic Uremic Syndrome: A Case Series in Pediatric Patients.

Selçuk Yüksel1, Havva Evrengül2, Z Birsin Özçakar3, Tülay Becerir2, Nagihan Yalçın4, Emine Korkmaz5, Fatih Ozaltin5.   

Abstract

INTRODUCTION: Studies relating to first-line, early, and long-term eculizumab treatment and outcomes in children with atypical hemolytic uremic syndrome (aHUS) are scarce and unclear. The aim of this case-series study was to evaluate the outcomes of first-line, early, and long-term eculizumab treatment in our aHUS patients.
MATERIALS AND METHODS: We reviewed the data from four pediatric patients with aHUS who were treated with eculizumab. In three of them, eculizumab was used as a first-line therapy, and the follow-up period was ≥2 years in three patients.
RESULTS: Plasma exchange could not be performed in any patient. Plasma infusions were used only in Patient 1 (a 14-month-old boy) for 8 days without any response. Therefore, eculizumab was started on day 11 after admission. Patient 2 (a 16-month-old boy), Patient 3 (an 11-year-old girl), and Patient 4 (a 32-month-old girl) were treated with eculizumab as a first-line therapy, which was started 2-4 days after admission. The dosage of eculizumab was adjusted according to body weight. The hematologic parameters (the time frames were 3-17 days) and C 3 (the time frames were 10-17 days) returned to normal in all patients after receipt of eculizumab. Although Patient 1 developed stage III chronic kidney disease, complete renal recovery occurred in Patients 2 and 4. Patient 3 also had reflux nephropathy with bilateral grade III vesicoureteral reflux and renal scars. Her creatinine clearance returned to the baseline value after receiving eculizumab. No complications related to eculizumab were observed in any patient during the follow-up period.
CONCLUSION: Eculizumab can be successfully used as a first-line therapy in pediatric aHUS patients. We observed that the early initiation of eculizumab was associated with the complete recovery of renal function.

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Year:  2016        PMID: 27646857     DOI: 10.1007/s40272-016-0194-0

Source DB:  PubMed          Journal:  Paediatr Drugs        ISSN: 1174-5878            Impact factor:   3.022


  31 in total

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Authors:  P Feng; S R Monday
Journal:  Mol Cell Probes       Date:  2000-12       Impact factor: 2.365

Review 2.  Atypical hemolytic-uremic syndrome.

Authors:  Marina Noris; Giuseppe Remuzzi
Journal:  N Engl J Med       Date:  2009-10-22       Impact factor: 91.245

Review 3.  Novel aspects of atypical haemolytic uraemic syndrome and the role of eculizumab.

Authors:  Jacobien C Verhave; Jack F M Wetzels; Nicole C A J van de Kar
Journal:  Nephrol Dial Transplant       Date:  2014-09       Impact factor: 5.992

Review 4.  Plasmatherapy in atypical hemolytic uremic syndrome.

Authors:  Chantal Loirat; Arnaud Garnier; Anne-Laure Sellier-Leclerc; Theresa Kwon
Journal:  Semin Thromb Hemost       Date:  2010-09-23       Impact factor: 4.180

5.  Eculizumab in the treatment of atypical hemolytic uremic syndrome in infants.

Authors:  Gema Ariceta; Beatriz Arrizabalaga; Mireia Aguirre; Elvira Morteruel; Margarita Lopez-Trascasa
Journal:  Am J Kidney Dis       Date:  2011-12-23       Impact factor: 8.860

6.  Autoimmune-type atypical hemolytic uremic syndrome treated with eculizumab as first-line therapy.

Authors:  Masataka Hisano; Akira Ashida; Eiji Nakano; Mamiko Suehiro; Yoko Yoshida; Masanori Matsumoto; Toshiyuki Miyata; Yoshihiro Fujimura; Motoshi Hattori
Journal:  Pediatr Int       Date:  2015-04       Impact factor: 1.524

7.  Eculizumab in atypical hemolytic uremic syndrome: long-term clinical course and histological findings.

Authors:  Sibylle Tschumi; Mathias Gugger; Barbara S Bucher; Magdalena Riedl; Giacomo D Simonetti
Journal:  Pediatr Nephrol       Date:  2011-08-30       Impact factor: 3.714

8.  Eculizumab therapy in a child with hemolytic uremic syndrome and CFI mutation.

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Journal:  Pediatr Nephrol       Date:  2012-08-19       Impact factor: 3.714

9.  Development of a multiplex PCR approach for the identification of Shiga toxin-producing Escherichia coli strains and their major virulence factor genes.

Authors:  J Osek
Journal:  J Appl Microbiol       Date:  2003       Impact factor: 3.772

10.  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

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  4 in total

1.  Complement factor B mutation-associated aHUS and myocardial infarction.

Authors:  Natália Noronha; Filipa Dias Costa; Andrea Dias; Alexandra Dinis
Journal:  BMJ Case Rep       Date:  2017-07-14

2.  Fatal meningococcemia due to Neisseria meningitidis serogroup Y in a vaccinated child receiving eculizumab.

Authors:  Meltem Polat; Selçuk Yüksel; Nuriye Ünal Şahin
Journal:  Hum Vaccin Immunother       Date:  2018-06-29       Impact factor: 3.452

3.  Atypical hemolytic uremic syndrome in first trimester pregnancy successfully treated with eculizumab.

Authors:  Gabriela Andries; Michael Karass; Srikanth Yandrapalli; Katherine Linder; Delong Liu; John Nelson; Rahul Pawar; Savneek Chugh
Journal:  Exp Hematol Oncol       Date:  2017-01-13

4.  Role of eculizumab in a pediatric refractory gemcitabine-induced thrombotic microangiopathy: a case report.

Authors:  Ludovica Facchini; Maurizio Lucchesi; Alessia Stival; Rosa Maria Roperto; Francesca Melosi; Marco Materassi; Silvia Farina; Veronica Tintori; Maurizio de Martino; Iacopo Sardi
Journal:  J Med Case Rep       Date:  2017-07-27
  4 in total

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