Exploring the patients' and family members' perspectives on home-based palliative care.

Nadia Sultanali Mushtaq
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Abstract

Background: Healthcare at home is considered a partial substitute for institutional long-term care, because patients and families with known poor prognoses prefer to stay home with their loved ones and are unable to pay for hospital care at the end of life in some countries.

Purpose: To explore patients' and family members' perspectives and experiences of receiving home-based palliative care services.

Method: This was a qualitative exploratory study conducted in Karachi, targeting patients and family members receiving home-based palliative care services. The data collection was done via interviews, and simultaneously, the interviewer recorded field notes, which were all carried out within the confines of the participants' homes. Moreover, the subjects were recruited through purposive sampling, resulting in a total of six patients and six family members. The final number of participants was determined based on data saturation. The inclusion criteria encompassed individuals of all genders, aged 18 and above, and residents of Karachi, Pakistan. Those who were not able to provide information, due to any reason, were excluded from the study. The study adhered strictly to ethical considerations.

Findings: The study uncovered several significant themes that provide valuable insights, including caregivers' availability, patients' inclusiveness, improved dietary pattern, psychological wellbeing, and rapid recovery in home-based care. Furthermore, the study identified themes on providing home-based palliative care, like family members' education and keeping back-ups for unforeseen situations. In contrast, the themes identified as home-based care preference over hospital care were: experienced compromised care, hospital anxiety, restricted to the available resources and higher hospital living expenses for patients and family members.

Conclusion: The study underscored the importance of adopting a patient-centric approach. It has become evident that the comfort and familiarity of one's home environment provide a conducive backdrop for holistic healing and wellbeing.

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探索病人和家属对居家姑息关怀的看法。
背景:在一些国家,预后不良的病人和家属更愿意留在家中陪伴亲人,而且无力支付生命末期的医院护理费用,因此居家医疗被认为是机构长期护理的部分替代品:这是一项在卡拉奇进行的定性探索性研究,研究对象是接受居家姑息关怀服务的患者和家属。数据收集是通过访谈进行的,同时,访谈者还记录了现场笔记,所有这些都是在参与者家中进行的。此外,研究对象是通过有目的的抽样方式招募的,最终共有 6 名患者和 6 名家属参与。最终的参与者人数是根据数据饱和度确定的。纳入标准包括所有性别、18 岁及以上、巴基斯坦卡拉奇居民。因任何原因无法提供信息的人都被排除在研究之外。研究严格遵守了道德规范:研究发现了几个重要的主题,提供了宝贵的见解,包括护理人员的可用性、患者的包容性、饮食模式的改善、心理健康以及家庭护理中的快速康复。此外,研究还发现了提供居家姑息关怀的主题,如家庭成员教育和为不可预见的情况保留后备人员。与此相反,与医院护理相比,居家护理更受患者青睐的主题包括:经历过受损的护理、医院焦虑、可用资源有限以及患者和家属的住院生活费用较高:这项研究强调了以病人为中心的重要性。家庭环境的舒适和熟悉程度显然为整体治疗和健康提供了有利的背景。
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