Inadequacy of cardiovascular risk factor management in chronic kidney transplantation - evidence from the FAVORIT study.

Categoría Estudio primario
RevistaClinical transplantation
Año 2012

Este artículo está incluido en 1 Revisión sistemática Revisiones sistemáticas (1 referencia) 1 Síntesis amplia Síntesis amplias (1 referencia)

Este artículo es parte de los siguientes hilos de publicación
  • FAVORIT [Folic Acid for Vascular Outcome Reduction in Transplant Trial] (12 documentos)
Este artículo es parte de las siguientes matrices de evidencia
Cargando información sobre las referencias

BACKGROUND:

Kidney transplant recipients (KTRs) have increased risk of cardiovascular disease (CVD). Our objective is to describe the prevalence of CVD risk factors applying standard criteria and use of CVD risk factor-lowering medications in contemporary KTRs.

METHODS:

The Folic Acid for Vascular Outcome Reduction in Transplantation study enrolled and collected medication data on 4107 KTRs with elevated homocysteine and stable graft function an average of five yr post-transplant.

RESULTS:

CVD risk factors were common (hypertension or use of blood pressure (BP) lowering medication in 92%, borderline or elevated low-density lipoprotein (LDL) or use of lipid-lowering agent in 66%, history of diabetes mellitus in 41%, and obesity in 38%); prevalent CVD was reported in 20% of study participants. National Kidney Foundation BP guidelines (BP <130/80 mmHg) were not met by 69% of participants. Uncontrolled hypertension (BP of 140/90 mmHg or higher) was present in 44% of those taking antihypertension medication; 18% of participants had borderline or elevated LDL, of which 60% were untreated, and 31% of the participants with prevalent CVD were not using an antiplatelet agent.

CONCLUSION:

There is opportunity to improve treatment and control of traditional CVD risk factors in kidney transplant recipients.
Epistemonikos ID: 036d7cbab1d056aec86d8e223d5b72bcbc6f9363
First added on: Jun 11, 2015