Early palliative care program in idiopathic pulmonary fibrosis patients favors at-home and hospice deaths, reduces unplanned medical visits, and prolongs survival: A pilot study.

IF 5.9 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL
European Journal of Internal Medicine Pub Date : 2024-10-01 Epub Date: 2024-05-23 DOI:10.1016/j.ejim.2024.05.024
Ilaria Bassi, Stefania Pastorello, Aldo Guerrieri, Gilda Giancotti, Anna Maria Cuomo, Chiara Rizzelli, Maria Coppola, Danila Valenti, Stefano Nava
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引用次数: 0

Abstract

Background: Idiopathic Pulmonary Fibrosis (IPF) is a lethal disease; most patients die in hospitals because palliative care (PC) is not wildly and early available. We aimed to determine the impact of an early PC program in IPF patients on place of death, emergency department (ED) admission, unplanned medical visits and survival before and after its implementation at our clinic.

Methods: IPF patients from our ILD clinic who died between January 1st, 2018 and December 31th, 2023 were included in the analysis. Primary outcomes were location of death, number of ED access and unplanned medical visits; secondary outcomes was survival from diagnosis.

Results: A total of 46 decedents between 2018 and 2023 were analysed: (median age 71,5 ± 5,5 years, 89 % male): 26 died before the implementation of the early PC program and 20 after. Through χ2 test, location of death resulted significantly different in the two groups, showing the capacity of early PC to favor at home or in hospice death (p = 0,02); similarly, the number of unplanned visits was significantly lower (p = 0,03). Finally, survival was significantly lower in patients not receiving the early PC program (p = 0,01).

Conclusion: The availability of an early PC program since the diagnosis significantly reduced both the death rate in hospital settings, favoring dying in hospice or at home, and the number of unplanned medical visits. Furthermore, IPF patients receiving early PC showed a longer survival than those who did not.

特发性肺纤维化患者早期姑息治疗计划有利于居家和临终关怀死亡,减少计划外就医,延长生存期:一项试点研究。
背景:特发性肺纤维化(IPF)是一种致死性疾病;由于姑息治疗(PC)不能普遍和及早提供,大多数患者死于医院。我们的目的是确定在本诊所实施早期姑息治疗计划前后,该计划对 IPF 患者的死亡地点、急诊科(ED)入院率、非计划就诊率和存活率的影响:分析对象包括在 2018 年 1 月 1 日至 2023 年 12 月 31 日期间死亡的 ILD 诊所 IPF 患者。主要结果为死亡地点、急诊室就诊次数和计划外就诊次数;次要结果为确诊后的存活率:结果:共分析了 2018 年至 2023 年间的 46 名死者(中位年龄为 71.5 ± 5.5 岁,89% 为男性):其中 26 人死于早期 PC 计划实施之前,20 人死于该计划实施之后。通过χ2检验,两组患者的死亡地点存在显著差异,这表明早期 PC 更有利于患者在家中或临终关怀机构死亡(p = 0,02);同样,非计划就诊次数也显著减少(p = 0,03)。最后,未接受早期 PC 计划的患者生存率明显降低(p = 0,01):结论:自确诊以来,早期 PC 计划的实施大大降低了患者在医院的死亡率,使其更倾向于在临终关怀机构或家中死亡,同时也减少了非计划就诊次数。此外,与未接受早期PC治疗的患者相比,接受早期PC治疗的IPF患者存活时间更长。
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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来源期刊
European Journal of Internal Medicine
European Journal of Internal Medicine 医学-医学:内科
CiteScore
9.60
自引率
6.20%
发文量
364
审稿时长
20 days
期刊介绍: The European Journal of Internal Medicine serves as the official journal of the European Federation of Internal Medicine and is the primary scientific reference for European academic and non-academic internists. It is dedicated to advancing science and practice in internal medicine across Europe. The journal publishes original articles, editorials, reviews, internal medicine flashcards, and other relevant information in the field. Both translational medicine and clinical studies are emphasized. EJIM aspires to be a leading platform for excellent clinical studies, with a focus on enhancing the quality of healthcare in European hospitals.
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