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Proton-pump inhibitor vs. H2-receptor blocker use and overall risk of CKD progression.
Cholin, Liza; Ashour, Tarek; Mehdi, Ali; Taliercio, Jonathan J; Daou, Remy; Arrigain, Susana; Schold, Jesse D; Thomas, George; Nally, Joseph; Nakhoul, Nazih L; Nakhoul, Georges N.
Afiliação
  • Cholin L; Cleveland Clinic, Cleveland, OH, USA. cholinl@ccf.org.
  • Ashour T; Cleveland Clinic, Cleveland, OH, USA.
  • Mehdi A; Cleveland Clinic, Cleveland, OH, USA.
  • Taliercio JJ; Cleveland Clinic, Cleveland, OH, USA.
  • Daou R; Saint-Joseph University, Beirut, Lebanon.
  • Arrigain S; Cleveland Clinic, Cleveland, OH, USA.
  • Schold JD; Cleveland Clinic, Cleveland, OH, USA.
  • Thomas G; Cleveland Clinic, Cleveland, OH, USA.
  • Nally J; Cleveland Clinic, Cleveland, OH, USA.
  • Nakhoul NL; Tulane University School of Medicine, New Orleans, LA, USA.
  • Nakhoul GN; Cleveland Clinic, Cleveland, OH, USA.
BMC Nephrol ; 22(1): 264, 2021 07 15.
Article em En | MEDLINE | ID: mdl-34266395
ABSTRACT

BACKGROUND:

The relationship between proton-pump inhibitor (PPI) use and chronic kidney disease (CKD) progression remains controversial. Specifically, there is a lack of data evaluating renal outcomes in established CKD patients. The aim of our study is to determine the risk of progression to end-stage kidney disease (ESKD) or death amongst CKD patients on PPI, histamine-2 receptor blocker (H2B), or no anti-acid therapy.

METHODS:

Using our CKD registry, we evaluated the relationship between PPI and H2B use and outcomes amongst patients with CKD (eGFR < 60), with at least 2 PCP visits in the year prior. A Cox proportional hazards model was used to evaluate the relationship between medication groups and overall mortality, while competing risks regression models were used to determine the risk of ESKD with death as a competing risk.

RESULTS:

25,455 patients met inclusion criteria and were stratified according to medication group no antacid therapy (15,961), PPI use (8646), or H2B use (848). At 4 years, the cumulative incidence of ESKD with death as a competing risk was 2.0% (95% CI 1.7, 2.4), 1.5% (0.8, 2.8), and 1.6%(1.4, 1.9) among PPI, H2B, and no medication respectively (P = 0.22). The cumulative incidence of death with ESKD as a competing risk was 17.6% (95% CI 16.6, 18.6), 16.7% (13.7, 19.8), and 17.3% (16.6, 18.0) (P = 0.71).

CONCLUSIONS:

Use of PPI in a CKD population was not associated with increased mortality or progression to ESKD when compared to H2 blocker and to no acid suppressing therapy.
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: Gastropatias / Insuficiência Renal Crônica / Inibidores da Bomba de Prótons / Antagonistas dos Receptores H2 da Histamina / Falência Renal Crônica Tipo de estudo: Diagnostic_studies / Etiology_studies / Incidence_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged País/Região como assunto: America do norte Idioma: En Revista: BMC Nephrol Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: Gastropatias / Insuficiência Renal Crônica / Inibidores da Bomba de Prótons / Antagonistas dos Receptores H2 da Histamina / Falência Renal Crônica Tipo de estudo: Diagnostic_studies / Etiology_studies / Incidence_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged País/Região como assunto: America do norte Idioma: En Revista: BMC Nephrol Ano de publicação: 2021 Tipo de documento: Article