Aims and objectives
To explore barriers to hepatocellular carcinoma screening among patients with hepatitis B.
Background
Hepatitis B‐related hepatocellular carcinoma is a major cause of cancer‐related mortality globally. A preventive strategy for screening is needed to improve early tumour detection and overall survival. However, utilisation remains suboptimal and barriers are understudied and largely focused on clinical factors.
Design
A qualitative study based on the preventive health model using phenomenological hermeneutical approach.
Methods
Face‐to‐face semi‐structured interviews were conducted with 23 hepatitis B patients from November 2020 to February 2021. Interpretative phenomenological analysis was used. The COREQ checklist was followed.
Results
Four themes were identified: (i) miscognition, (ii) cultural stigma and taboo, (iii) social norms of enduring hardship and (iv) social barriers at the community, health system and policy levels. Patients had misconceptions about inactive carriers, asymptomatic nature of chronic hepatitis B, hepatocellular carcinoma risks and screening recommendations. Influenced by the taboo of hepatocellular carcinoma, stigma against hepatitis B and enduring hardship norms, they perceived screening as divination, avoided utilisation to hide disease status and endured symptoms until they were intolerable. Insufficient community support, a lack of shared decision‐making in health systems, and inadequate rural reimbursement policy and hepatocellular carcinoma detection capacity further precluded utilisation.
Conclusions
Cognitive and sociocultural barriers precluded individuals’ intention, utilisation and persistence of hepatocellular carcinoma screening. The results highlight intervention targets for miscognition, stigma, taboo and social norms; propose family‐focused, community‐based education programs; suggest health systems to introduce decision aids; and inform policymaking and upskilling of physicians in rural areas.
Relevance to clinical practice
Collaborative efforts are needed to improve real‐world hepatocellular carcinoma screening, including education to address knowledge deficiencies, psychological counselling to reduce stigma and taboo beliefs, support for shared decision‐making and reimbursement policies.