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Efficacy and tolerability of febuxostat in gout patients on dialysis.
Choi, See Y; Choi, Seung W; Lee, Sunggun; So, Min W; Oh, Ji S; Lim, Doo-Ho.
Afiliación
  • Choi SY; Division of Rheumatology, Department of Internal Medicine, University of Ulsan College of Medicine, Ulsan University Hospital, Ulsan, South Korea.
  • Choi SW; Division of Rheumatology, Department of Internal Medicine, University of Ulsan College of Medicine, Ulsan University Hospital, Ulsan, South Korea.
  • Lee S; Division of Rheumatology, Department of Internal Medicine, Haeundae Paik Hospital, Inje University College of Medicine, Busan, South Korea.
  • So MW; Division of Rheumatology, Department of Internal Medicine, Pusan National University Yangsan Hospital, Yangsan, South Korea.
  • Oh JS; Department of Biomedical Informatics, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea.
  • Lim DH; Division of Rheumatology, Department of Internal Medicine, University of Ulsan College of Medicine, Ulsan University Hospital, Ulsan, South Korea.
Intern Med J ; 51(3): 348-354, 2021 Mar.
Article en En | MEDLINE | ID: mdl-32043690
ABSTRACT

BACKGROUND:

There are no sufficient data available on the use of febuxostat in patients undergoing dialysis.

AIM:

To investigate the efficacy and tolerability of febuxostat in gout patients on dialysis.

METHODS:

We retrospectively reviewed clinical and laboratory data available from a referral centre from January 2012 to December 2018. We included gout patients who initiated febuxostat during dialysis. Data regarding serum uric acid levels before and after the febuxostat treatment and clinical information such as gout attack after febuxostat initiation, as well as adverse events involving febuxostat treatment, were obtained from medical records.

RESULTS:

Among 62 patients who were treated with febuxostat for over 3 months, 45 were undergoing haemodialysis (HD) and 17 were undergoing peritoneal dialysis (PD). The mean serum uric acid level was significantly reduced 3 months after treatment (3.71 ± 1.32 mg/dL) compared with that at the pretreatment level (9.36 ± 2.06 mg/dL) (P < 0.001). The serum uric acid level was observed to be significantly reduced at 3 months in both HD and PD patients and subsequently remained at a significantly reduced level for 12 months. Of the 62 patients, only two stopped febuxostat due to its adverse effects. Initial dose of 80 mg/day was associated with higher adverse events compared to dose of 20-40 mg/day (odds ratio 8.25, 95% confidence interval 1.90-35.97, P = 0.006).

CONCLUSIONS:

Febuxostat is efficacious and well tolerated in gout patients on dialysis. Febuxostat taken at dose of 20-40 mg/day might be appropriate initial dose in patients undergoing dialysis.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Hiperuricemia / Gota Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Intern Med J Asunto de la revista: MEDICINA INTERNA Año: 2021 Tipo del documento: Article País de afiliación: Corea del Sur

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Hiperuricemia / Gota Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Intern Med J Asunto de la revista: MEDICINA INTERNA Año: 2021 Tipo del documento: Article País de afiliación: Corea del Sur