Palliative Care Needs and Responses Among Lung Cancer Patients: Insights from a Provincial Hospital in Vietnam.

An Minh Nguyen, Linh Dieu Ha, Linh Phuong Nguyen, Long Hoang Vo
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Abstract

Background: Cancer remains a global health challenge, with rising incidence and mortality rates despite advancements in prevention and treatment. In 2022, cancer was the second leading cause of death worldwide, contributing to approximately 9.7 million deaths and 20 million new cases.

Objective: This study evaluates the palliative care needs and responses among lung cancer patients, aiming to inform healthcare policies and enhance palliative care delivery in Vietnam.

Methods: A cross-sectional descriptive study was conducted at a provincial hospital from February to October 2024. The study included 204 lung cancer patients aged ≥18 years, capable of providing informed consent and participating in interviews. Data were collected using a validated questionnaire grounded in national palliative care guidelines, assessing eight domains: physical, psychological, informational, daily activities, communication, spiritual care, self-management, and social welfare needs. The tool exhibited excellent reliability (Cronbach's alpha: 0.74-0.97).

Results: Among 204 participants, 75% were ≥60 years old, with a male predominance (72.5%) and rural residency (85.3%). Educational attainment was generally low (51% with lower secondary or below), and the majority were farmers (67.2%). Most patients were in advanced disease stages (Stage III: 38.2%; Stage IV: 32.4%). Physical needs, such as breathing difficulty relief (82.3%), and social interaction (86.8%) were predominant. Psychological needs, particularly anxiety reduction, were reported by 74.5%. Notably, 85.3% required clear medical explanations, and 90.2% sought better disease-related communication. While self-management (90.2%) and financial support (90.7%) were the most effectively addressed needs, spiritual care received the least attention, with 66.2% of patients reporting unmet needs and only 37.7% receiving adequate support.

Conclusion: The findings underscore critical gaps in palliative care, especially in spiritual, psychological, and financial support. A holistic, patient-centered approach integrating spiritual care, rehabilitation, and enhanced social support is essential. Improved access to specialized services through telemedicine and outreach programs is vital for rural patients. These results call for policy reform and strengthened healthcare infrastructure to meet the comprehensive needs of lung cancer patients. Future studies should evaluate the long-term outcomes of targeted palliative interventions.

肺癌患者的姑息治疗需求和反应:来自越南一家省级医院的见解。
背景:癌症仍然是一个全球性的健康挑战,尽管在预防和治疗方面取得了进展,但发病率和死亡率仍在上升。2022年,癌症是全球第二大死因,造成约970万人死亡和2000万新病例。目的:本研究评估肺癌患者的姑息治疗需求和反应,旨在为越南的医疗政策提供信息并加强姑息治疗的提供。方法:采用横断面描述性研究,于2024年2月- 10月在某省立医院进行。研究纳入204例年龄≥18岁、能够提供知情同意并参与访谈的肺癌患者。数据收集使用基于国家姑息治疗指南的有效问卷,评估八个领域:身体、心理、信息、日常活动、沟通、精神护理、自我管理和社会福利需求。该工具具有良好的可靠性(Cronbach's alpha: 0.74-0.97)。结果:204名参与者中,年龄≥60岁的占75%,男性居多(72.5%),农村居民占85.3%。受教育程度普遍较低(51%为初中及以下),大多数是农民(67.2%)。大多数患者处于疾病晚期(III期:38.2%;IV期:32.4%)。身体需求,如呼吸困难缓解(82.3%)和社会互动(86.8%)占主导地位。74.5%的人报告了心理需求,特别是减少焦虑。值得注意的是,85.3%的人需要明确的医学解释,90.2%的人寻求更好的疾病相关沟通。虽然自我管理(90.2%)和经济支持(90.7%)是最有效的需求,但精神护理得到的关注最少,66.2%的患者报告需求未得到满足,只有37.7%的患者得到足够的支持。结论:研究结果强调了姑息治疗的关键差距,特别是在精神、心理和经济支持方面。一个整体的,以病人为中心的方法整合精神护理,康复,并加强社会支持是必不可少的。通过远程医疗和外展方案改善获得专业服务的机会对农村患者至关重要。这些结果呼吁政策改革和加强卫生保健基础设施,以满足肺癌患者的综合需求。未来的研究应评估有针对性的姑息性干预的长期结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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