Literature DB >> 33051945

High level of medication adherence is required to lower mortality in patients with chronic hepatitis B taking entecavir: A nationwide cohort study.

Jayoun Lee1, Songhee Cho1, Hyo Jeong Kim1, Hangil Lee2, Min Jung Ko1, Young-Suk Lim1,3.   

Abstract

It is unclear whether suboptimal adherence contributes to adverse clinical outcomes in patients with chronic hepatitis B (CHB). Moreover, there is no consensus regarding the optimal level of drug adherence. This was a population-based historical cohort study including 51 975 adult CHB patients treated with entecavir (0.5 mg/d orally). Data were obtained from the Korean national health insurance service claims database, which covers >99% of the entire population, between 2007 and 2015. Medication adherence was categorized as high (proportion of days covered [PDC], ≥90%; n = 32 089), intermediate (PDC, 80%-89%; n = 10 197) and low (PDC, <80%; n = 9689). During a median 4.5 years (maximal 9 years) of follow-up in 51 975 CHB patients treated with entecavir, multivariable analyses revealed that the risk of mortality/transplantation was significantly greater in the low-adherers (adjusted hazard ratio [HR], 1.38; P < .001) and intermediate-adherers (adjusted HR, 1.44; P < .001) than the high-adherers (P for trend < 0.001). The risk of renal failure in the low- and intermediate-adherence groups was also significantly higher than the high-adherence group (P for trend < 0.001). By contrast, the risk of hepatocellular carcinoma (HCC) was not significantly different between groups (P for trend = 0.70). The higher risk of mortality/transplantation and renal failure but similar risk of HCC for low- and intermediate-adherers compared with high-adherers was consistent in inverse probability treatment weighting analysis of the entire cohort and subcohorts with or without cirrhosis. In conclusion, high medication adherence (≥90%) is required to significantly lower risk of mortality and renal failure in patients with CHB during long-term treatment with entecavir.
© 2020 John Wiley & Sons Ltd.

Entities:  

Keywords:  entecavir; hepatitis B virus; hepatocellular carcinoma; mortality; proportion of days covered

Year:  2020        PMID: 33051945     DOI: 10.1111/jvh.13418

Source DB:  PubMed          Journal:  J Viral Hepat        ISSN: 1352-0504            Impact factor:   3.728


  3 in total

1.  APASL guidance on stopping nucleos(t)ide analogues in chronic hepatitis B patients.

Authors:  Jia-Horng Kao; Tung-Hung Su; Wen-Juei Jeng; Qin Ning; Tai-Chung Tseng; Yoshiyuki Ueno; Man-Fung Yuen
Journal:  Hepatol Int       Date:  2021-07-23       Impact factor: 6.047

2.  Risk of hepatocellular carcinoma in antiviral treatment-naïve chronic hepatitis B patients treated with entecavir or tenofovir disoproxil fumarate: a network meta-analysis.

Authors:  Ze-Hong Huang; Gui-Yang Lu; Ling-Xian Qiu; Guo-Hua Zhong; Yue Huang; Xing-Mei Yao; Xiao-Hui Liu; Shou-Jie Huang; Ting Wu; Quan Yuan; Ying-Bin Wang; Ying-Ying Su; Jun Zhang; Ning-Shao Xia
Journal:  BMC Cancer       Date:  2022-03-17       Impact factor: 4.430

Review 3.  Review article: switching patients with chronic hepatitis B to tenofovir alafenamide-a review of current data.

Authors:  Young-Suk Lim; Wai-Kay Seto; Masayuki Kurosaki; Scott Fung; Jia-Horng Kao; Jinlin Hou; Stuart C Gordon; John F Flaherty; Leland J Yee; Yang Zhao; Kosh Agarwal; Pietro Lampertico
Journal:  Aliment Pharmacol Ther       Date:  2022-02-17       Impact factor: 9.524

  3 in total

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