Choice of Acid Suppressant Therapy and Long-Term Graft Outcomes After Kidney Transplantation.


Journal

Pharmacotherapy
ISSN: 1875-9114
Titre abrégé: Pharmacotherapy
Pays: United States
ID NLM: 8111305

Informations de publication

Date de publication:
11 2020
Historique:
pubmed: 11 10 2020
medline: 4 9 2021
entrez: 10 10 2020
Statut: ppublish

Résumé

The purpose of this study was to comprehensively evaluate the long-term adverse effects of proton pump inhibitors (PPIs) compared with histamine-2 receptor antagonists (H2RAs) in kidney transplant recipients. This retrospective cohort compared 582 patients treated with PPI with 705 patients treated with H2RA and evaluated adverse effects throughout their course of acid suppressant therapy to a maximum of nine years posttransplant. The primary outcome of interest was renal function at 1 year posttransplant; secondary outcomes included renal function at 30 days, 3, 5, and 9 years posttransplant as well as rejection, electrolyte and laboratory abnormalities, osteoporosis, pneumonia, and Clostridium difficile infections. Renal function did not significantly differ at any timepoint posttransplant. Rejection rates and Clostridium difficile infections were similar between groups; osteoporosis and pneumonia rates were numerically higher in the PPI treated arm but did not reach statistical significance. Proton pump inhibitor (PPI) treated patients were more likely to experience hypomagnesemia requiring supplementation. High dose PPI treated patients had significantly higher rates of pneumonia and osteoporosis compared with H2RA treated patients. Patients were maintained on PPI therapy for an average of 5 years and H2RA therapy for 3 years posttransplant, the majority without a clear indication for therapy. There was no difference in renal function, rejection, or graft loss between PPI and H2RA treated patients. The majority of patients were maintained on PPI therapy for several years posttransplant without a clear indication; critical evaluation of ongoing need for acid suppressant therapy in the posttransplant course should be an area of future focus.

Identifiants

pubmed: 33037663
doi: 10.1002/phar.2470
doi:

Substances chimiques

Histamine H2 Antagonists 0
Proton Pump Inhibitors 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1082-1088

Informations de copyright

© 2020 Pharmacotherapy Publications, Inc.

Références

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Auteurs

Spenser E January (SE)

Department of Pharmacy, Barnes-Jewish Hospital, Saint Louis, Missouri, USA.

Kristin Progar (K)

Department of Pharmacy, Barnes-Jewish Hospital, Saint Louis, Missouri, USA.

Nicole M Nesselhauf (NM)

Department of Pharmacy, Barnes-Jewish Hospital, Saint Louis, Missouri, USA.

Jennifer C Hagopian (JC)

Department of Pharmacy, Barnes-Jewish Hospital, Saint Louis, Missouri, USA.

Andrew F Malone (AF)

Division of Nephrology, Washington University Physicians, Saint Louis, Missouri, USA.

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