Goals of care and advance directives: A 1-year retrospective analysis of a tertiary centre in Saudi Arabia.

International journal of palliative nursing Pub Date : 2026-03-02 Epub Date: 2026-03-20 DOI:10.12968/ijpn.2025.0078
Steven Callaghan, Kim Sadler, Gassan Abudari, Kholoud Alhassan, Muneerah Almutairi, Ruth Evangelista, Mahmoud Sroor, Goncalo Placido, Lemon Bacalso, Mohammed AlGhamdi, Bashayer Albayjan, Lubna Shaltoot, Reema Alomari, Mohammed Azuny, Amjad Alsubaie
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Abstract

Background: Despite its limited therapeutic value, high costs and the fact that it can compromise a patient's quality of life, aggressive care continues to be provided at the end of life. It has been associated with a significant symptom burden for patients, a greater use of healthcare resources, delay in accessing palliative care programmes and personal/family and healthcare costs.

Aim: To investigate sociodemographic, clinical and community healthcare service factors associated with aggressive end-of-life care across malignant and non-malignant conditions.

Method: A 1-year retrospective analysis was conducted in a tertiary care centre in Saudi Arabia. All deaths of adult patients that occurred between 1 January, 2023 and 1 January, 2024, were included. Data were retrieved from medical charts, including sociodemographics, medical history, invasive medical interventions and use of healthcare services in the last 3 months of life.

Results: The study included 590 adults (mean age 59.6 years; 52.2% male), with 62% diagnosed with malignancy. The majority (71%) had one or more chronic comorbidities. In their last 90 days, 48.6% were admitted to the intensive care unit. Advance directives were present for only half of the patients included in this study. Non-malignant patients received significantly more aggressive end-of-life care, including intubation and cardiopulmonary resuscitation. Palliative care referrals were low overall (48.1%), but higher in cases of malignancy (70.5%). Patients with involvement in a palliative care team showed a lower symptom burden and less aggressive treatment.

Conclusions: These findings suggest unequal access to end-of-life advocates for earlier palliative care referral, which could reduce aggressive treatments, especially for younger patients with non-malignant diseases. Non-cancer referral rates were low, highlighting a need for further collaboration and integration with palliative care services.

护理目标和预先指示:1年回顾性分析在沙特阿拉伯的第三中心。
背景:尽管其治疗价值有限,费用高,而且可能影响患者的生活质量,但在生命末期仍继续提供积极治疗。它与患者的严重症状负担、更多地使用医疗保健资源、获得姑息治疗方案的延迟以及个人/家庭和医疗保健费用有关。目的:调查与恶性和非恶性疾病患者积极临终关怀相关的社会人口学、临床和社区卫生保健服务因素。方法:在沙特阿拉伯的一家三级保健中心进行了为期1年的回顾性分析。包括2023年1月1日至2024年1月1日期间发生的所有成年患者死亡。从医疗图表中检索数据,包括社会人口统计学、病史、侵入性医疗干预和生命最后3个月的医疗服务使用情况。结果:该研究纳入590名成年人(平均年龄59.6岁,52.2%为男性),其中62%诊断为恶性肿瘤。大多数(71%)有一种或多种慢性合并症。48.6%的患者在最后90天入住重症监护病房。在这项研究中,只有一半的患者有预先指示。非恶性患者接受更积极的临终关怀,包括插管和心肺复苏。姑息治疗转诊总体较低(48.1%),但恶性肿瘤转诊较高(70.5%)。参与姑息治疗小组的患者表现出较低的症状负担和较少的积极治疗。结论:这些研究结果表明,在早期姑息治疗转诊中,获得临终倡导者的机会不平等,这可以减少积极的治疗,特别是对于患有非恶性疾病的年轻患者。非癌症转诊率较低,突出表明需要进一步与姑息治疗服务合作和整合。
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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