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本文引用的文献

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When to initiate early palliative care? Challenges faced by healthcare providers.何时开始早期姑息治疗?医疗服务提供者面临的挑战。
Front Med (Lausanne). 2023 Oct 2;10:1220370. doi: 10.3389/fmed.2023.1220370. eCollection 2023.
2
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J Palliat Med. 2024 Mar;27(3):411-420. doi: 10.1089/jpm.2023.0263. Epub 2023 Sep 13.
3
Stability of clinical prediction models developed using statistical or machine learning methods.基于统计或机器学习方法开发的临床预测模型的稳定性。
Biom J. 2023 Dec;65(8):e2200302. doi: 10.1002/bimj.202200302. Epub 2023 Jul 19.
4
European Respiratory Society clinical practice guideline: palliative care for people with COPD or interstitial lung disease.欧洲呼吸学会临床实践指南:COPD 或间质性肺疾病患者的姑息治疗。
Eur Respir J. 2023 Aug 17;62(2). doi: 10.1183/13993003.02014-2022. Print 2023 Aug.
5
Global Initiative for Chronic Obstructive Lung Disease 2023 Report: GOLD Executive Summary.慢性阻塞性肺疾病全球倡议组织2023年报告:《慢性阻塞性肺疾病全球倡议》执行摘要
Am J Respir Crit Care Med. 2023 Apr 1;207(7):819-837. doi: 10.1164/rccm.202301-0106PP.
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Mortality and comorbidities in patients with bronchiectasis over a 3-year follow-up.支气管扩张症患者在 3 年随访期间的死亡率和合并症。
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8
External validation of the GAP model in Chinese patients with idiopathic pulmonary fibrosis.中文特发性肺纤维化患者 GAP 模型的外部验证。
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Syndrome of Combined Pulmonary Fibrosis and Emphysema: An Official ATS/ERS/JRS/ALAT Research Statement.特发性肺纤维化合并肺气肿综合征:美国胸科学会/欧洲呼吸学会/日本呼吸学会/拉丁美洲胸科学会联合官方声明。
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Developing, validating, updating and judging the impact of prognostic models for respiratory diseases.开发、验证、更新和评判呼吸系统疾病预后模型的影响。
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慢性肺病预后模型(PRO-MEL):建立和时间验证。

The PROgnostic ModEl for chronic lung disease (PRO-MEL): development and temporal validation.

机构信息

Health Services and Outcomes Research, National Healthcare Group, Annex @ National Skin Centre, 1 Mandalay Road, Singapore, 308205, Singapore.

Department of Palliative Medicine, Tan Tock Seng Hospital, 11 Jalan Tan Tock Seng, Singapore, 308433, Singapore.

出版信息

BMC Pulm Med. 2024 Aug 30;24(1):429. doi: 10.1186/s12890-024-03233-0.

DOI:10.1186/s12890-024-03233-0
PMID:39215286
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11365240/
Abstract

BACKGROUND

Patients with chronic lung diseases (CLDs), defined as progressive and life-limiting respiratory conditions, experience a heavy symptom burden as the conditions become more advanced, but palliative referral rates are low and late. Prognostic tools can help clinicians identify CLD patients at high risk of deterioration for needs assessments and referral to palliative care. As current prognostic tools may not generalize well across all CLD conditions, we aim to develop and validate a general model to predict one-year mortality in patients presenting with any CLD.

METHODS

A retrospective cohort study of patients with a CLD diagnosis at a public hospital from July 2016 to October 2017 was conducted. The outcome of interest was all-cause mortality within one-year of diagnosis. Potential prognostic factors were identified from reviews of prognostic studies in CLD, and data was extracted from electronic medical records. Missing data was imputed using multiple imputation by chained equations. Logistic regression models were developed using variable selection methods and validated in patients seen from January 2018 to December 2019. Discriminative ability, calibration and clinical usefulness of the model was assessed. Model coefficients and performance were pooled across all imputed datasets and reported.

RESULTS

Of the 1000 patients, 122 (12.2%) died within one year. Patients had chronic obstructive pulmonary disease or emphysema (55%), bronchiectasis (38%), interstitial lung diseases (12%), or multiple diagnoses (6%). The model selected through forward stepwise variable selection had the highest AUC (0.77 (0.72-0.82)) and consisted of ten prognostic factors. The model AUC for the validation cohort was 0.75 (0.70, 0.81), and the calibration intercept and slope were - 0.14 (-0.54, 0.26) and 0.74 (0.53, 0.95) respectively. Classifying patients with a predicted risk of death exceeding 0.30 as high risk, the model would correctly identify 3 out 10 decedents and 9 of 10 survivors.

CONCLUSIONS

We developed and validated a prognostic model for one-year mortality in patients with CLD using routinely available administrative data. The model will support clinicians in identifying patients across various CLD etiologies who are at risk of deterioration for a basic palliative care assessment to identify unmet needs and trigger an early referral to palliative medicine.

TRIAL REGISTRATION

Not applicable (retrospective study).

摘要

背景

慢性肺部疾病(CLD)患者的病情呈进行性发展且危及生命,随着病情的发展,他们的症状负担很重,但姑息治疗的转诊率很低且很滞后。预后工具可以帮助临床医生识别出病情恶化风险较高的 CLD 患者,以便进行需求评估并转至姑息治疗。由于当前的预后工具可能无法很好地适用于所有 CLD 疾病,因此我们旨在开发和验证一种可预测任何 CLD 患者一年内死亡率的通用模型。

方法

对 2016 年 7 月至 2017 年 10 月在一家公立医院就诊的 CLD 患者进行回顾性队列研究。感兴趣的结局是诊断后一年内的全因死亡率。从 CLD 的预后研究综述中确定了潜在的预后因素,并从电子病历中提取了数据。使用链状方程的多重插补法对缺失数据进行了插补。使用变量选择方法开发了逻辑回归模型,并在 2018 年 1 月至 2019 年 12 月就诊的患者中进行了验证。评估了模型的判别能力、校准和临床实用性。在所有插补数据集中汇总了模型系数和性能,并进行了报告。

结果

在 1000 名患者中,有 122 名(12.2%)在一年内死亡。患者患有慢性阻塞性肺疾病或肺气肿(55%)、支气管扩张症(38%)、间质性肺疾病(12%)或多种诊断(6%)。通过逐步向前变量选择选择的模型具有最高的 AUC(0.77(0.72-0.82)),并包含十个预后因素。验证队列的模型 AUC 为 0.75(0.70,0.81),校准截距和斜率分别为-0.14(-0.54,0.26)和 0.74(0.53,0.95)。将预测死亡风险超过 0.30 的患者分类为高危患者,该模型将正确识别出 10 名死者中的 3 名和 10 名幸存者中的 9 名。

结论

我们使用常规可用的行政数据为 CLD 患者开发并验证了一种用于预测一年内死亡率的预后模型。该模型将有助于临床医生识别出各种 CLD 病因的患者,这些患者的病情恶化风险较高,需要进行基本的姑息治疗评估,以确定未满足的需求并尽早转至姑息医学。

试验注册

不适用(回顾性研究)。