Virtual monitoring for stable chronic hepatitis B patients does not reduce adherence to medications: A randomised controlled study

Author:

Kumar Rajneesh12ORCID,Yee Mei-Ling3,Goh George BB12,Chia Pei-Yuh4,Lee Hwei-Ling4,Xin X5,Teo Pek SE5,Ekstrom Victoria SM12,Tan Jin YT12,Cheah Mark CC12ORCID,Wang Yu T12,Chang Jason PE12,Tan Chee-Keat12ORCID,Tan Hiang Keat12,Krishnamoorthy Thinesh L12,Chow Wan-Cheng12

Affiliation:

1. Department of Gastroenterology and Hepatology, Singapore General Hospital, Singapore

2. Duke-NUS Medical School, Singapore

3. Department of Pharmacy, Singapore General Hospital, Singapore

4. Department of Nursing, Singapore General Hospital, Singapore

5. Health Services Research Unit, Research Office, Singapore General Hospital, Singapore

Abstract

Introduction Chronic hepatitis B (CHB) remains common in endemic regions, causing significant healthcare burden. Patients with CHB may need to be adherent to nucleoside analogue (NA) for a long period of time to prevent complications. This study aims to investigate the safety, efficacy and patient experience of a virtual monitoring clinic (VMC) in monitoring stable patients taking NA for CHB. Methods Patients on NA and regular follow-up were randomised to either VMC alternating with doctors’ clinic visit or to a control group in which they continued standard follow-up by doctors. Therapy adherence was measured by medication possession ratio (MPR) for NA therapy, incidence of virological breakthrough and hepatocellular carcinoma (HCC) development at two years of follow-up. Patient acceptance was measured on a Likert scale of 1–10. Results A total 192 patients completed follow-up: 94 and 98 patients in the VMC and control groups, respectively. Mean age was 60.6 ± 10.8 years, with 95.3% Chinese ethnicity and 64.1% males. Age, gender, race, educational, employment and financial status were similar in both groups. Upon study completion, the majority of patients – 76 (80.9%) in VMC group and 74 (75.5%) in control group – had MPR ≥0.8; 88.8% were satisfied and rated VMC better than a traditional follow-up clinic with doctors only. More than 85% of patients rated ≥8/10 on the Likert scale for VMC, and preferred VMC over traditional clinic visits. Clinical outcomes observed were HCC development in one (1.1%) in the VMC group and four (4.1%) in the control group ( p = 0.369). Two (2.1%) and one (1.0%) virological breakthroughs were observed in the VMC and control groups, respectively ( p = 0.615). No incidence of HCC or abnormal blood tests were missed in the VMC arm. Discussion VMC is a viable and safe clinical model for monitoring stable CHB patients on NA therapy without compromising patients’ adherence to medications and is preferred by patients.

Funder

SingHealth Foundation

Publisher

SAGE Publications

Subject

Health Informatics

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