Effects of a lower versus a higher oxygenation target in intensive care unit patients with chronic obstructive pulmonary disease and acute hypoxaemic respiratory failure: a subgroup analysis of a randomised clinical trial

Maria B. Nielsen , Thomas L. Klitgaard , Ulla M. Weinreich , Frederik M. Nielsen , Anders Perner , Olav L. Schjørring , Bodil S. Rasmussen
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引用次数: 0

Abstract

Background

Oxygen supplementation is ubiquitous in intensive care unit (ICU) patients with chronic obstructive pulmonary disease (COPD) and acute hypoxaemia, but the optimal oxygenation target has not been established.

Methods

This was a pre-planned subgroup analysis of the Handling Oxygenation Targets in the ICU (HOT-ICU) trial, which allocated patients with acute hypoxaemia to a lower oxygenation target (partial pressure of arterial oxygen [Pao2] of 8 kPa) vs a higher target (Pao2 of 12 kPa) during ICU admission, for up to 90 days; the allocation was stratified for presence or absence of COPD. Here, we report key outcomes for patients with COPD.

Results

The HOT-ICU trial enrolled 2928 patients of whom 563 had COPD; 277 were allocated to the lower and 286 to the higher oxygenation group. After allocation, the median Pao2 was 9.1 kPa (inter-quartile range 8.7–9.9) in the lower group vs 12.1 kPa (11.2–12.9) in the higher group. Data for arterial carbon dioxide (Paco2) were available for 497 patients (88%) with no between-group difference in time-weighted average; median Paco2 6.0 kPa (5.2–7.2) in the lower group vs 6.2 kPa (5.4–7.3) in the higher group. At 90 days, 122/277 patients (44%) in the lower oxygenation group had died vs 132/285 patients (46%) in the higher (relative risk 0.98; 95% confidence interval 0.82–1.17; P=0.67). No statistically significant differences were found in any secondary outcome.

Conclusions

In ICU patients with COPD and acute hypoxaemia, a lower vs a higher oxygenation target did not reduce mortality. There were no between-group differences in Paco2 or in secondary outcomes.

Clinical trial registration

NCT 03174002, EudraCT number 2017-000632-34.

对患有慢性阻塞性肺病和急性低氧血症呼吸衰竭的重症监护室患者采用较低与较高氧合目标的效果:随机临床试验的亚组分析
背景在患有慢性阻塞性肺病(COPD)和急性低氧血症的重症监护病房(ICU)患者中,补氧无处不在,但最佳氧合目标尚未确定。该试验将急性低氧血症患者分配到一个较低的氧合目标(动脉氧分压 [Pao2] 为 8 kPa)与一个较高的氧合目标(Pao2 为 12 kPa),持续时间长达 90 天。结果 HOT-ICU 试验招募了 2928 名患者,其中 563 人患有慢性阻塞性肺病;277 人被分配到低氧组,286 人被分配到高氧组。分配后,低氧组的 Pao2 中位数为 9.1 kPa(四分位间范围为 8.7-9.9),高氧组为 12.1 kPa(11.2-12.9)。497名患者(88%)提供了动脉二氧化碳(Paco2)数据,时间加权平均值无组间差异;中位数 Paco2 低分组为 6.0 kPa(5.2-7.2),高分组为 6.2 kPa(5.4-7.3)。90 天时,低氧组有 122/277 名患者(44%)死亡,而高氧组有 132/285 名患者(46%)死亡(相对风险 0.98;95% 置信区间 0.82-1.17;P=0.67)。结论 在患有慢性阻塞性肺病和急性低氧血症的重症监护病房患者中,较低与较高氧合目标并不能降低死亡率。临床试验注册号NCT 03174002,EudraCT号2017-000632-34。
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来源期刊
BJA open
BJA open Anesthesiology and Pain Medicine
CiteScore
0.60
自引率
0.00%
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审稿时长
83 days
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