Artigo Acesso aberto Revisado por pares

Outcomes of kidney transplantation in Alport syndrome compared with other forms of renal disease

2016; Taylor & Francis; Volume: 39; Issue: 1 Linguagem: Inglês

10.1080/0886022x.2016.1262266

ISSN

1525-6049

Autores

Yvelynne P. Kelly, Anish Patil, Luke Wallis, Susan Murray, Sam Kant, Mohammed A. Kaballo, Liam Casserly, Brendan Doyle, Anthony Dorman, Patrick O’Kelly, Peter J. Conlon,

Tópico(s)

Renal and Vascular Pathologies

Resumo

Alport syndrome is an inherited renal disease characterized by hematuria, renal failure, hearing loss and a lamellated glomerular basement membrane. Patients with Alport syndrome who undergo renal transplantation have been shown to have patient and graft survival rates similar to or better than those of patients with other renal diseases.In this national case series, based in Beaumont Hospital Dublin, we studied the cohort of patients who underwent renal transplantation over the past 33 years, recorded prospectively in the Irish Renal Transplant Registry, and categorized them according to the presence or absence of Alport syndrome. The main outcomes assessed were patient and renal allograft survival.Fifty-one patients diagnosed with Alport syndrome in Beaumont Hospital received 62 transplants between 1982 and 2014. The comparison group of non-Alport patients comprised 3430 patients for 3865 transplants. Twenty-year Alport patient survival rate was 70.2%, compared to 44.8% for patients with other renal diseases (p = .01). Factors associated with patient survival included younger age at transplantation as well as differences in recipient sex, donor age, cold ischemia time, and episodes of acute rejection. Twenty-year graft survival was 46.8% for patients with Alport syndrome compared to 30.2% for those with non-Alport disease (p = .11).Adjusting for baseline differences between the groups, patients with end-stage kidney disease (ESKD) due to Alport syndrome have similar patient and graft survival to those with other causes of ESKD. This indicates that early diagnosis and management can lead to favorable outcomes for this patient cohort.

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