COPD患者长期无创通气:一项回顾性队列研究。

R Broadhead, S Mukherjee, V Aiyappan, C Chai-Coetzer, S Ullah, A Walker
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摘要

居家长期无创通气(LT-NIV)是重度慢性阻塞性肺疾病(COPD)和慢性高碳酸血症患者公认的治疗方法。这项研究的目的是对开始接受LT-NIV治疗的COPD患者进行特征分析。方法回顾性分析2016年6月至2022年3月澳大利亚某三级医院所有经主治医生诊断为COPD的患者。结果333例患者开始接受LT-NIV治疗,其中67例(20%)患有COPD。住院患者LT-NIV开始:53/67(79%)患者在COPD急性加重住院期间开始使用LT-NIV。患者为老年人(平均69±SD 9.5岁),以女性为主(60%),伴中重度COPD (FEV1 37±18%)和轻中度合并症负担(Charlson共病指数评分2.1±1.4)。在LT-NIV之前,有64%的患者进行睡眠研究,其中15%的患者患有严重的OSA (AHI≥30或ODI≥30)。30%以前需要急性NIV。入院前无加重PaCO2为58±7.3mmHg,入院时所有住院患者均表现为高碳酸血症(PaCO2≥45mmHg)。住院患者PaCO2峰值为87±20mmHg,出院时持续高碳酸血症58±9.0mmHg。出院时,IPAP和EPAP设置分别为17±3.8和7.7cm±2.7cmH2O。在开始使用LT-NIV后的12个月内,呼吸相关和全因住院率无显著降低(p分别=0.66和0.53)。本研究说明了我们中心在现实世界中使用LT-NIV治疗慢性阻塞性肺病的情况,其中大多数是在住院时开始使用的,而不是早期门诊重新评估。需要一项前瞻性多中心分析来更好地了解慢性阻塞性肺病患者LT-NIV处方的细微差别。
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P063 Long-term Non-invasive Ventilation in Patients with COPD: A Retrospective Cohort Study.
Abstract Introduction Domiciliary long-term non-invasive ventilation (LT-NIV) is an accepted therapy for patients with severe chronic obstructive pulmonary disease (COPD) and chronic hypercapnia. This study aimed to characterise patients with COPD who were commenced on LT-NIV. Methods A retrospective analysis was performed of all patients prescribed LT-NIV with a primary physician-diagnosis of COPD, between June 2016 and March 2022 at an Australian tertiary hospital. Results 333 patients were commenced on LT-NIV, of whom 67 (20%) had COPD. Inpatient LT-NIV Initiation: 53/67 (79%) were commenced on LT-NIV during an inpatient admission with acute exacerbation of COPD. Patients were elderly (age, mean 69± SD 9.5 years), predominantly female (60%) with moderate-severe COPD (FEV1 37±18%) and mild-moderate comorbidity burden (Charlson Comorbidity Index Score 2.1±1.4). Prior to LT-NIV, 64% patients had a sleep study with 15% having severe OSA (AHI≥30 or ODI≥30). 30% previously required acute NIV. Pre-admission non-exacerbated PaCO2 was 58±7.3mmHg During admission, all inpatients demonstrated hypercapnia (PaCO2≥45mmHg). Peak inpatient PaCO2 was 87±20mmHg, with persistent hypercapnia on discharge 58±9.0mmHg. On discharge, IPAP and EPAP settings were 17±3.8 and 7.7cm±2.7cmH2O respectively. There was a non-significant reduction in respiratory-related and all-cause hospitalizations in the 12-months following LT-NIV initiation (p=0.66 and 0.53 respectively). Outpatient LT-NIV Initiation: [Further data collection in progress] Discussion This study illustrates the real-world prescription of LT-NIV for COPD at our centre, with the majority being initiated in the inpatient setting, rather than early outpatient reassessment. A prospective multi-centre analysis is required to better understand the nuances of LT-NIV prescription in patients with COPD.
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