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特发性肺纤维化患者生命末期的医疗费用。试点多学科协作性间质性肺疾病临床诊疗中心的评估。

Health Care Costs at the End of Life for Patients with Idiopathic Pulmonary Fibrosis. Evaluation of a Pilot Multidisciplinary Collaborative Interstitial Lung Disease Clinic.

机构信息

Division of Pulmonary Medicine, Department of Medicine, Faculty of Medicine and Dentistry, and.

Alberta Health Services, Edmonton, Alberta, Canada; and.

出版信息

Ann Am Thorac Soc. 2020 Jun;17(6):706-713. doi: 10.1513/AnnalsATS.201909-707OC.

DOI:10.1513/AnnalsATS.201909-707OC
PMID:32197048
Abstract

Even though idiopathic pulmonary fibrosis (IPF) is a disease with high morbidity and mortality and no cure, palliative care is rarely implemented, leading to high symptom burden and unmet care needs. In 2012, we implemented a multidisciplinary collaborative (MDC) care model linking clinic and community multidisciplinary teams to provide an early integrated palliative approach, focusing on early symptom management and advance care planning. To evaluate the differences in resource use and associated costs of end-of-life care between patients with IPF who received early integrated palliative care and patients with IPF who received conventional treatment. Using administrative health data, we identified all patients in the Province of Alberta, Canada, who presented to a hospital with an IPF diagnosis between January 1, 2012, and December 31, 2018, and died within this time frame. We compared three groups of patients: those who received MDC care (our clinic patients), specialist care (SC; respirologist), or non-specialist care (NSC; no contact with a respiratory clinic). The primary outcomes were healthcare resource use and costs in the year before death. Of 2,768 patients across the three study groups, in the last year of life, MDC patients were more than three times as likely as SC patients to have received antifibrotic therapies (odds ratio [OR], 3.0; 95% confidence interval [CI], 1.8-5.2), almost twice as likely to have received pulmonary rehabilitation (OR, 1.9; 95% CI, 1.1-3.4), and 36% more likely to have received opiates (OR, 1.4; 95% CI, 0.8-2.3). The median total healthcare costs in the last 3 months of life were approximately C$7,700 lower for MDC patients than for those receiving SC, driven primarily by fewer hospitalizations and emergency department visits. MDC patients were also less likely to die in the hospital (44.9% MDC vs. 64.9% SC vs. 66.8% NSC;  < 0.001) and had the highest rates of no hospitalization in the last year of life. An integrated palliative approach in IPF is associated with improvements in the quality of end-of-life care and reduction in costs. Transformation of care models is required to deliver palliative care for patients with IPF. MDC teams within such models can address the high burden of unmet needs for symptom management, advance care planning, and community support in this complex population.

摘要

尽管特发性肺纤维化 (IPF) 是一种发病率和死亡率高且尚无治愈方法的疾病,但姑息治疗很少实施,导致症状负担高和护理需求未得到满足。2012 年,我们实施了多学科协作 (MDC) 护理模式,将诊所和社区多学科团队联系起来,提供早期综合姑息治疗方法,重点关注早期症状管理和预先护理计划。评估接受早期综合姑息治疗的特发性肺纤维化患者与接受常规治疗的特发性肺纤维化患者在生命末期护理方面的资源利用和相关成本差异。使用行政健康数据,我们确定了 2012 年 1 月 1 日至 2018 年 12 月 31 日期间在加拿大艾伯塔省的一家医院就诊并在此期间内死亡的所有特发性肺纤维化患者。我们比较了三组患者:接受 MDC 护理(我们的诊所患者)、专科护理(SC;肺病专家)或非专科护理(NSC;与呼吸科诊所无联系)的患者。主要结局是死亡前一年的医疗资源利用和成本。在三个研究组的 2768 名患者中,在生命的最后一年,MDC 患者接受抗纤维化治疗的可能性是 SC 患者的三倍多(比值比 [OR],3.0;95%置信区间 [CI],1.8-5.2),接受肺康复的可能性几乎是 SC 患者的两倍(OR,1.9;95%CI,1.1-3.4),接受阿片类药物的可能性高 36%(OR,1.4;95%CI,0.8-2.3)。MDC 患者在生命的最后 3 个月的总医疗费用中位数比接受 SC 治疗的患者低约 7700 加元,这主要是由于住院和急诊就诊次数减少。MDC 患者也不太可能在医院死亡(44.9% MDC 与 64.9% SC 与 66.8% NSC;<0.001),并且在生命的最后一年住院率最低。在 IPF 中采用综合姑息治疗方法可改善生命末期护理质量并降低成本。需要改变护理模式,为 IPF 患者提供姑息治疗。此类模型中的 MDC 团队可以解决该复杂人群中症状管理、预先护理计划和社区支持方面的高未满足需求负担。

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