Back to Search Start Over

Proton pump inhibitor usage reduces sustained viral response rates for veterans with HIV/HCV coinfection on ledipasvir/sofosbuvir: a real-world study from a multicentre VA cohort

Authors :
William E. Bryan
Tzu-Hao Lee
Austin Chan
Mary L. Townsend
Cynthia A. Moylan
Susanna Naggie
Steve S. Choi
Mohamed G. Hashem
Lawrence P. Park
Rachel B. Britt
Source :
J Viral Hepat
Publication Year :
2020

Abstract

Background Previous studies have reported an association of proton pump inhibitor (PPI) use and decreased sustained viral response rate (SVR) in patients taking ledipasvir/sofosbuvir (LDV/SOF). The relationship between PPI usage and SVR is less clear in patients with HIV/HCV coinfection, where concomitant antiretrovirals may result in more complex drug interactions. Aims Evaluate the effects of acid suppression medications (PPI or H2 -receptor antagonist [H2 B]) use and SVR rates in patients with HIV/HCV or HCV and taking LDV/SOF in a large multi-center veteran cohort. Methods Retrospective analysis of all veterans in the Veterans Affairs Health Care System who received LDV/SOF ± ribavirin from 10/10/2014 to 12/31/2015. The odds ratios (OR) of PPI or H2 B use for SVR were adjusted for clinical factors and with inverse probability of treatment weighting for non-random treatment selection for acid suppression medication use. Results There were 9703 veterans included in our final analysis. After adjustment of other clinical factors, PPI use is associated with a lower SVR in the overall cohort (95.0% vs. 96.1%, OR:0.86, 95% CI: 0.74-0.99, P=0.03, number needed to harm 90.9) and HIV/HCV co-infection subgroup (93.4% vs. 96.9%, OR:0.47, 95% CI: 0.26-0.85, P=0.01, number needed to harm 28.6). Conclusion PPI use is associated with reduced SVR after LDV/SOF treatment, with a more significant impact in the subgroup of patients with HIV/HCV coinfection. Precautions need to be taken when using PPI and LDV/SOF in this group of patients.

Details

ISSN :
13652893
Volume :
28
Issue :
4
Database :
OpenAIRE
Journal :
Journal of viral hepatitis
Accession number :
edsair.doi.dedup.....f27e0d64b9d2990325c47f263a648b7b