UMeHealth Unit, Faculty of Medicine, University of Malaya (UM), Kuala Lumpur, Malaysia.
Department of Family Medicine, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia (UPM), Kuala Lumpur, Malaysia.
Health Expect. 2022 Dec;25(6):2837-2850. doi: 10.1111/hex.13590. Epub 2022 Sep 13.
Shared decision-making has been shown to improve the quality of life in metastatic breast cancer patients in high-literacy and high-resource settings. However, limited studies have examined the cultural preferences of metastatic breast cancer patients with shared decision-making implementation and the barriers encountered in an Asian setting where societal norms predominate and physician decision-making is at the forefront. This paper aims to identify (1) barriers to practising shared decision-making faced by healthcare professionals and patients and (2) strategies for implementing shared decision-making in the context of metastatic breast cancer management in Malaysia.
We conducted a qualitative study involving 12 patients diagnosed with metastatic breast cancer, 16 healthcare professionals and 5 policymakers from surgical and oncology departments at public healthcare centres in Malaysia. Semi-structured in-depth interviews and focus group discussions were conducted. The interviews were recorded, transcribed verbatim and analysed using the thematic approach. Nvivo software was used to manage and analyse the data.
Five main themes emerged from the study: healthcare provider-patient communication, workforce availability, cultural and belief systems, goals of care and paternalism versus autonomy. Other strategies proposed to overcome barriers to implementing shared decision-making were training of healthcare professionals and empowering nurses to manage patients' psychosocial issues.
This study found that practising shared decision-making in the public health sector remains challenging when managing patients with metastatic breast cancer. The utilization of decision-making tools, patient empowerment and healthcare provider training may help address the system and healthcare provider-patient barriers identified in this study.
Patients were involved in the study design, recruitment and analysis.
在高文化和高资源环境中,共享决策已被证明可以改善转移性乳腺癌患者的生活质量。然而,有限的研究考察了在以社会规范为主导和医生决策处于前沿的亚洲环境中,转移性乳腺癌患者在实施共享决策时的文化偏好和遇到的障碍。本文旨在确定:(1)医疗保健专业人员和患者在实践共享决策时面临的障碍;(2)在马来西亚转移性乳腺癌管理背景下实施共享决策的策略。
我们进行了一项定性研究,参与者包括 12 名被诊断患有转移性乳腺癌的患者、16 名医疗保健专业人员和 5 名来自马来西亚公共医疗中心外科和肿瘤学部门的政策制定者。进行了半结构化深入访谈和焦点小组讨论。访谈进行了录音,逐字记录,并使用主题方法进行分析。使用 Nvivo 软件管理和分析数据。
从研究中出现了五个主要主题:医护人员与患者的沟通、劳动力可用性、文化和信仰体系、护理目标以及家长式作风与自主权。为克服实施共享决策的障碍而提出的其他策略包括对医疗保健专业人员进行培训以及授权护士来管理患者的社会心理问题。
本研究发现,在公共卫生部门管理转移性乳腺癌患者时,实践共享决策仍然具有挑战性。决策工具的使用、患者赋权和医疗保健提供者培训可能有助于解决本研究中确定的系统和医疗保健提供者-患者障碍。
患者参与了研究设计、招募和分析。