Department of Emergency, Second Affiliated Hospital of Chongqing Medical University, Chongqing 400010, China.
Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2024 Feb 28;49(2):266-272. doi: 10.11817/j.issn.1672-7347.2024.230329.
Patients with acute exacerbation of chronic obstructive pulmonary disease (AECOPD) combined with severe type II respiratory failure have a high probability of ventilation failure using conventional non-invasive positive pressure ventilation (NPPV). This study aims to investigate the clinical efficacy of high intensity NPPV (HI-NPPV) for the treatment of AECOPD combined with severe type II respiratory failure.
The data of patients with AECOPD combined with severe type II respiratory failure (blood gas analysis pH≤7.25) treated with NPPV in the Second Affiliated Hospital of Chongqing Medical University from July 2013 to July 2023 were collected to conduct a retrospective case-control study. The patients were divided into 2 groups according to the inspired positive airway pressure (IPAP) used during the NPPV treatment: a NPPV group (IPAP<20 cmHO, 1 cmHO=0.098 kPa) and a HI-NPPV group (20 cmHO≤IPAP< 30 cmHO). Ninety-nine and 95 patients were included in the NPPV group and the HI-NPPV group, respectively. A total of 86 pairs of data were matched using propensity score matching (PSM) for data matching. The primary outcome indexes (mortality and tracheal intubation rate) and secondary outcome indexes [blood gas analysis pH, arterial partial pressure of oxygen (PaO) and arterial partial pressure of carbon dioxide (PaCO), adverse reaction rate, and length of hospitalization] were compared between the 2 groups.
The tracheal intubation rates of the NPPV group and the HI-NPPV group were 6.98% and 1.16%, respectively, and the difference between the 2 groups was statistically significant (=4.32, <0.05); the mortality of the NPPV group and the HI-NPPV group was 23.26% and 9.30%, respectively, and the difference between the 2 groups was statistically significant (=11.64, <0.01). The PaO at 24 h and 48 h after treatment of the HI-NPPV group was higher than that of the NPPV group, and the PaCO of the HI-NPPV group was lower than that of the NPPV group, and the differences were statistically significant (all <0.05). The differences of pH at 24 h and 48 h after treatment between the 2 groups were not statistically significant (both >0.05). The differences between the 2 groups in adverse reaction rate and hospitalization length were not statistically significant (both >0.05).
HI-NPPV can reduce mortality and tracheal intubation rates by rapidly improving the ventilation of patients with AECOPD combined with severe type II respiratory failure. This study provides a new idea for the treatment of patients with AECOPD combined with severe type II respiratory failure.
慢性阻塞性肺疾病急性加重(AECOPD)合并严重 II 型呼吸衰竭患者使用常规无创正压通气(NPPV)发生通气失败的概率较高。本研究旨在探讨高强度 NPPV(HI-NPPV)治疗 AECOPD 合并严重 II 型呼吸衰竭的临床疗效。
收集 2013 年 7 月至 2023 年 7 月重庆医科大学附属第二医院收治的 AECOPD 合并严重 II 型呼吸衰竭(血气分析 pH 值≤7.25)患者应用 NPPV 治疗的临床资料,进行回顾性病例对照研究。根据 NPPV 治疗时使用的吸气正压(IPAP)将患者分为 2 组:NPPV 组(IPAP<20 cmH2O,1 cmH2O=0.098 kPa)和 HI-NPPV 组(20 cmH2O≤IPAP<30 cmH2O)。NPPV 组和 HI-NPPV 组分别纳入 99 例和 95 例患者。采用倾向性评分匹配(PSM)对数据进行匹配,共匹配 86 对数据。比较两组患者的主要结局指标(病死率和气管插管率)和次要结局指标[血气分析 pH 值、动脉血氧分压(PaO2)和动脉血二氧化碳分压(PaCO2)、不良反应发生率和住院时间]。
NPPV 组和 HI-NPPV 组的气管插管率分别为 6.98%和 1.16%,两组比较差异有统计学意义(=4.32,<0.05);NPPV 组和 HI-NPPV 组的病死率分别为 23.26%和 9.30%,两组比较差异有统计学意义(=11.64,<0.01)。HI-NPPV 组治疗后 24 h 和 48 h 的 PaO2 均高于 NPPV 组,PaCO2 均低于 NPPV 组,差异均有统计学意义(均<0.05)。两组治疗后 24 h 和 48 h 的 pH 值比较差异均无统计学意义(均>0.05)。两组不良反应发生率和住院时间比较差异均无统计学意义(均>0.05)。
HI-NPPV 可通过迅速改善 AECOPD 合并严重 II 型呼吸衰竭患者的通气,降低病死率和气管插管率。本研究为 AECOPD 合并严重 II 型呼吸衰竭患者的治疗提供了新的思路。