Literature DB >> 30205388

Eculizumab Modifies Outcomes in Adults with Atypical Hemolytic Uremic Syndrome with Acute Kidney Injury.

Mercedes Cao1, Bruna N Leite1, Tamara Ferreiro1, María Calvo1, Constantino Fernández1, Ángel Alonso1, Alejandro Rodriguez1, Pilar Salvador2, Rocío Seijo3, Salvador Pita3, Emilia Arjona4, Santiago Rodríguez de Córdoba4, Francisco Valdés Cañedo1.   

Abstract

BACKGROUND: Atypical hemolytic uremic syndrome (aHUS) is a rare disease associated with congenital or acquired genetic abnormalities that result in uncontrolled complement activation, leading to thrombotic microangiopathy and kidney failure. Until recently, the only treatment was plasma exchange or plasma infusion (PE/PI), but 60% of patients died or had permanent kidney damage despite treatment. Eculizumab, a complement inhibitor, has shown promising results in aHUS. However, data are mainly extracted from case reports or studies of heterogeneous cohorts, and no direct comparison with PE/PI is available.
METHODS: An observational retrospective study of adult, dialysis-dependent aHUS patients with acute kidney injury (AKI) who were treated with either PE/PI alone or with second-line eculizumab in our center. We compared the effect of PE/PI and eculizumab on kidney function, hypertension, proteinuria, hematologic values, relapse, and death.
RESULTS: Thirty-one patients were included (females, 18; sporadic aHUS, 29; mean age, 46 ± 20 years). Twenty-six patients were treated with PE/PI alone, and 5 were deemed to be plasma-resistant and received eculizumab after stopping PE/PI. Among patients receiving eculizumab, 80% attained complete recovery of kidney function, 100% stopped dialysis, 20% had decreased proteinuria, and no patient relapsed (vs. 38.5, 50, 15.4, and 11.5%, respectively, of patients receiving only PE/PI). At 1-year of follow-up, no deaths had occurred in either group.
CONCLUSION: Eculizumab shows greater efficacy than PE/PI alone for the treatment of adult aHUS patients with AKI. Prospective studies and meta-analyses are warranted to confirm our findings and set guidelines for treatment, monitoring, and maintenance.
© 2018 S. Karger AG, Basel.

Entities:  

Keywords:  Acute kidney injury; Atypical hemolytic uremic syndrome; Complement pathway; Eculizumab; Plasma therapy

Year:  2018        PMID: 30205388     DOI: 10.1159/000492865

Source DB:  PubMed          Journal:  Am J Nephrol        ISSN: 0250-8095            Impact factor:   3.754


  4 in total

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Journal:  Ren Fail       Date:  2022-12       Impact factor: 3.222

2.  Interventions for atypical haemolytic uraemic syndrome.

Authors:  Dan Pugh; Eoin D O'Sullivan; Fiona Ai Duthie; Philip Masson; David Kavanagh
Journal:  Cochrane Database Syst Rev       Date:  2021-03-23

3.  Atypical Hemolytic Uremic Syndrome after SARS-CoV-2 Infection: Report of Two Cases.

Authors:  Iwona Smarz-Widelska; Małgorzata Syroka-Główka; Joanna Janowska-Jaremek; Małgorzata M Kozioł; Wojciech Załuska
Journal:  Int J Environ Res Public Health       Date:  2022-09-11       Impact factor: 4.614

4.  Optimal management of atypical hemolytic uremic disease: challenges and solutions.

Authors:  Rupesh Raina; Manpreet K Grewal; Yeshwanter Radhakrishnan; Vineeth Tatineni; Meredith DeCoy; Linda Lg Burke; Arvind Bagga
Journal:  Int J Nephrol Renovasc Dis       Date:  2019-09-04
  4 in total

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