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Interstitial lung disease and specialist palliative care access: a healthcare professionals survey.间质性肺病与专科姑息治疗的可及性:一项医疗专业人员调查。
BMJ Support Palliat Care. 2022 Dec;12(e6):e748-e751. doi: 10.1136/bmjspcare-2019-002148. Epub 2020 Jun 19.
2
Validation of the surprise question in gynecologic oncology: A one-question screen to promote palliative care integration and advance care planning.验证妇科肿瘤学中的意外问题:一个问题的筛查,以促进姑息治疗的整合和预先护理计划。
Gynecol Oncol. 2020 Jun;157(3):754-758. doi: 10.1016/j.ygyno.2020.03.007. Epub 2020 Mar 12.
3
Early referral to palliative care services in patients with IPF: a tool to take a step forward.特发性肺纤维化患者早期转诊至姑息治疗服务:向前迈进的一项工具。
BMJ Support Palliat Care. 2022 Jul;12(e2):e277-e278. doi: 10.1136/bmjspcare-2019-001980. Epub 2019 Aug 29.
4
The added value of comorbidities in predicting survival in idiopathic pulmonary fibrosis: a multicentre observational study.合并症在特发性肺纤维化生存预测中的附加值:一项多中心观察性研究。
Eur Respir J. 2019 Mar 7;53(3). doi: 10.1183/13993003.01587-2018. Print 2019 Mar.
5
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Eur J Heart Fail. 2019 Feb;21(2):227-234. doi: 10.1002/ejhf.1353. Epub 2018 Dec 11.
6
Diagnosis of Idiopathic Pulmonary Fibrosis. An Official ATS/ERS/JRS/ALAT Clinical Practice Guideline.特发性肺纤维化诊断。美国胸科学会/欧洲呼吸学会/日本呼吸学会/拉丁美洲胸科学会临床实践指南。
Am J Respir Crit Care Med. 2018 Sep 1;198(5):e44-e68. doi: 10.1164/rccm.201807-1255ST.
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Idiopathic Pulmonary Fibrosis.特发性肺纤维化
N Engl J Med. 2018 May 10;378(19):1811-1823. doi: 10.1056/NEJMra1705751.
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mMRC dyspnoea scale indicates impaired quality of life and increased pain in patients with idiopathic pulmonary fibrosis.改良英国医学研究委员会呼吸困难量表表明,特发性肺纤维化患者的生活质量受损且疼痛加剧。
ERJ Open Res. 2017 Dec 14;3(4). doi: 10.1183/23120541.00084-2017. eCollection 2017 Oct.
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Psychometric validation of the needs assessment tool: progressive disease in interstitial lung disease.需求评估工具:间质性肺疾病进展性疾病的心理测量验证。
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Beyond Idiopathic Pulmonary Fibrosis Diagnosis: Multidisciplinary Care With an Early Integrated Palliative Approach Is Associated With a Decrease in Acute Care Utilization and Hospital Deaths.除特发性肺纤维化诊断外:采用早期综合姑息治疗的多学科护理与急性护理利用减少和医院死亡减少相关。
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《疑问问题对特发性肺纤维化一年死亡率预测的价值:一项前瞻性队列研究》

The Value of the Surprise Question to Predict One-Year Mortality in Idiopathic Pulmonary Fibrosis: A Prospective Cohort Study.

机构信息

Department of Respiratory Medicine, Erasmus Medical Center, Rotterdam, The Netherlands.

Erasmus MC Cancer Institute, Department of Medical Oncology, Rotterdam, The Netherlands.

出版信息

Respiration. 2021;100(8):780-785. doi: 10.1159/000516291. Epub 2021 May 27.

DOI:10.1159/000516291
PMID:34044401
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8491469/
Abstract

BACKGROUND

Idiopathic pulmonary fibrosis (IPF) is a progressive fatal disease with a heterogeneous disease course. Timely initiation of palliative care is often lacking. The surprise question "Would you be surprised if this patient died within the next year?" is increasingly used as a clinical prognostic tool in chronic diseases but has never been evaluated in IPF.

OBJECTIVE

We aimed to evaluate the predictive value of the surprise question for 1-year mortality in IPF.

METHODS

In this prospective cohort study, clinicians answered the surprise question for each included patient. Clinical parameters and mortality data were collected. The sensitivity, specificity, accuracy, negative, and positive predictive value of the surprise question with regard to 1-year mortality were calculated. Multivariable logistic regression analysis was performed to evaluate which factors were associated with mortality. In addition, discriminative performance of the surprise question was assessed using the C-statistic.

RESULTS

In total, 140 patients were included. One-year all-cause mortality was 20% (n = 28). Clinicians identified patients with a survival of <1 year with a sensitivity of 68%, a specificity of 82%, an accuracy of 79%, a positive predictive value of 49%, and a negative predictive value of 91%. The surprise question significantly predicted 1-year mortality in a multivariable model (OR 3.69; 95% CI 1.24-11.02; p = 0.019). The C-statistic of the surprise question to predict mortality was 0.75 (95% CI 0.66-0.85).

CONCLUSIONS

The answer on the surprise question can accurately predict 1-year mortality in IPF. Hence, this simple tool may enable timely focus on palliative care for patients with IPF.

摘要

背景

特发性肺纤维化(IPF)是一种进行性致命疾病,其病程具有异质性。姑息治疗往往不能及时开始。“如果这个患者在未来一年内去世,你会感到惊讶吗?”这个意外问题越来越多地被用作慢性疾病的临床预后工具,但从未在 IPF 中进行过评估。

目的

我们旨在评估意外问题对 IPF 患者 1 年死亡率的预测价值。

方法

在这项前瞻性队列研究中,临床医生为每位纳入的患者回答意外问题。收集临床参数和死亡率数据。计算意外问题对 1 年死亡率的敏感性、特异性、准确性、阴性预测值和阳性预测值。进行多变量逻辑回归分析,以评估哪些因素与死亡率相关。此外,还使用 C 统计量评估意外问题的判别性能。

结果

共纳入 140 名患者。1 年全因死亡率为 20%(n=28)。临床医生确定了生存期<1 年的患者,其敏感性为 68%,特异性为 82%,准确性为 79%,阳性预测值为 49%,阴性预测值为 91%。意外问题在多变量模型中显著预测 1 年死亡率(OR 3.69;95%CI 1.24-11.02;p=0.019)。意外问题预测死亡率的 C 统计量为 0.75(95%CI 0.66-0.85)。

结论

意外问题的答案可以准确预测 IPF 的 1 年死亡率。因此,这种简单的工具可以使 IPF 患者及时关注姑息治疗。