Chai Andrew, Csoma Balazs, Lazar Zsofia, Bentley Andrew, Bikov Andras
Division of Immunology, Immunity to Infection and Respiratory Medicine, University of Manchester, Manchester M13 9PL, UK.
Wythenshawe Hospital, Manchester University NHS Foundation Trust, Manchester M23 9LT, UK.
J Clin Med. 2024 Sep 22;13(18):5624. doi: 10.3390/jcm13185624.
: There is a growing concern that opioids and benzodiazepines can depress the respiratory drive and could contribute to worsening respiratory failure and higher exacerbation frequency in COPD. However, the relationship between the exacerbation rate and medication taken is poorly understood in patients with chronic respiratory failure due to COPD. : As part of a service evaluation project, we analysed 339 patients with COPD who were established on long-term non-invasive ventilation (LT-NIV) at our tertiary centre. We investigated the relationship between benzodiazepine and opioid prescription and clinical outcomes as well as their impact on the exacerbation rate and overall survival following setup. : Before LT-NIV setup, 40 patients took benzodiazepines and 99 patients took opioids. Neither benzodiazepine nor opioid use was associated with changes in daytime blood gases, overnight hypoxia or annual exacerbations before NIV setup, but patients taking opioids were more breathless as assessed by modified Medical Research Council scores (3.91 ± 0.38 vs. 3.65 ± 0.73, < 0.01). Long-term NIV significantly reduced the number of yearly exacerbations (from 3.0/2.0-5.0/ to 2.8/0.71-4.57/, < 0.01) in the whole cohort, but the effect was limited in those who took benzodiazepines (from 3.0/2.0-7.0/ to 3.5/1.2-5.5/) or opioids (3.0/2.0-6.0/ to 3.0/0.8-5.5/). Benzodiazepine use was associated with reduced exacerbation-free survival and overall survival (both < 0.05). However, after adjustment with relevant covariates, the relationship with exacerbation-free survival became insignificant ( = 0.12). Opioids were not associated with adverse outcomes. : Benzodiazepines and opiates are commonly taken in this cohort. Whilst they do not seem to contribute to impaired gas exchange pre-setup, they, especially benzodiazepines, may limit the benefits of LT-NIV.
人们越来越担心阿片类药物和苯二氮䓬类药物会抑制呼吸驱动,并可能导致慢性阻塞性肺疾病(COPD)患者的呼吸衰竭恶化和急性加重频率增加。然而,对于因COPD导致慢性呼吸衰竭的患者,急性加重率与所服用药物之间的关系却知之甚少。作为一项服务评估项目的一部分,我们分析了在我们三级中心接受长期无创通气(LT-NIV)治疗的339例COPD患者。我们研究了苯二氮䓬类药物和阿片类药物处方与临床结局之间的关系,以及它们对开始治疗后的急性加重率和总生存率的影响。在开始LT-NIV治疗前,40例患者服用苯二氮䓬类药物,99例患者服用阿片类药物。在开始无创通气治疗前,使用苯二氮䓬类药物或阿片类药物均与日间血气变化、夜间低氧或年度急性加重无关,但根据改良的医学研究委员会评分评估,服用阿片类药物的患者呼吸急促更为明显(3.91±0.38对3.65±0.73,P<0.01)。长期无创通气显著降低了整个队列中的年度急性加重次数(从3.0/2.0 - 5.0/降至)2.8/0.71 - 4.57/,P<0.01),但对服用苯二氮䓬类药物的患者(从3.0/2.0 - 7.0/降至3.5/1.2 - 5.5/)或服用阿片类药物的患者(从3.0/2.0 - 6.0/降至3.0/0.8 - 5.5/)效果有限。使用苯二氮䓬类药物与无急性加重生存期和总生存期缩短相关(均P<0.05)。然而,在对相关协变量进行调整后,与无急性加重生存期的关系变得不显著(P = 0.12)。阿片类药物与不良结局无关。在这个队列中,患者普遍服用苯二氮䓬类药物和阿片类药物。虽然它们似乎在治疗前不会导致气体交换受损,但它们,尤其是苯二氮䓬类药物,可能会限制长期无创通气的益处。