异丙嗪在伴有和不伴有哮喘的严重慢性阻塞性肺病患者中的镇静抗组胺治疗:一项全国性登记研究中的死亡和严重恶化

IF 1.8 Q3 RESPIRATORY SYSTEM
Barbara Bonnesen, Valdemar Rømer, Sidse Graff Jensen, Jon Torgny Wilcke, Julie Janner, Jens Bak, Sofie Johansson, Christian B Laursen, Lars Pedersen, Josefin Eklof, Pradeesh Sivapalan, Jens-Ulrik Stæhr Jensen
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引用次数: 0

摘要

背景:镇静抗组胺药如异丙嗪被用作慢性阻塞性肺疾病(COPD)伴或不伴哮喘患者的抗焦虑药和催眠药,尽管对其作用和副作用的了解有限。我们评估异丙嗪治疗是否有较低的有害后果风险。方法:在全国范围内对丹麦专家诊断的门诊COPD患者进行回顾性队列研究,这些患者使用异丙嗪或活性比较物(褪黑激素)治疗。收集异丙嗪或褪黑素的患者倾向评分为1:1匹配。通过Cox比例风险回归分析,主要结局是严重COPD恶化和全因死亡的综合结果。我们对共病哮喘进行了相互作用分析。结果:在56,523例COPD患者的登记中,5,661例收集了异丙嗪(n = 3,723)或褪黑素(n = 1,938)。3,290名异丙嗪或褪黑激素治疗的患者进行了1:1的配对,可用于初步分析。在1年内,异丙嗪治疗的患者发生主要结局的风险高于对照组,风险比(HR)为1.42 (CI 1.27-1.58, p p p = 0.19)。对整个人群进行校正后的Cox分析表明,服用异丙嗪的风险进一步增加(在服用异丙嗪≥400片/年的患者中,主要结局HR =2.15, CI 1.94-2.38)。结论:与褪黑激素相比,异丙嗪治疗的COPD患者存在严重恶化和全因死亡的复合结局风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Sedating antihistamine treatment with promethazine in patients with severe COPD with and without asthma: death and severe exacerbations in a nationwide register study.

Sedating antihistamine treatment with promethazine in patients with severe COPD with and without asthma: death and severe exacerbations in a nationwide register study.

Sedating antihistamine treatment with promethazine in patients with severe COPD with and without asthma: death and severe exacerbations in a nationwide register study.

Sedating antihistamine treatment with promethazine in patients with severe COPD with and without asthma: death and severe exacerbations in a nationwide register study.

Background: Sedating antihistamines such as promethazine are used as anxiolytics and hypnotic agents for patients with chronic obstructive pulmonary disease (COPD) with and without asthma despite limited knowledge of its effects and side effects. We evaluated if treatment with promethazine had a lower risk of harmful outcome.

Methods: Nationwide retrospective cohort study of Danish specialist diagnosed outpatients with COPD treated with promethazine or an active comparator (melatonin). Patients with collection of promethazine or melatonin were propensity score matched 1:1. The primary outcome was a composite of severe COPD exacerbations and death from all causes analyzed by Cox proportional hazards regression. We performed an interaction analysis for comorbid asthma.

Results: In our registry of 56,523 patients with COPD, 5,661 collected promethazine (n = 3,723) or melatonin (n = 1,938). A cohort of 3,290 promethazine- or melatonin-treated patients matched 1:1 was available for the primary analysis.Within 1-year patients treated with promethazine were at higher risk of the primary outcome than matched controls with a Hazard Ratio (HR) of 1.42 (CI 1.27-1.58, p < 0.0001). Similarly, the risk of death was higher for promethazine-treated patients (HR 1.53, CI 1.32-1.77, p < 0.0001). An interaction analysis for comorbid asthma showed no interaction between comorbid asthma and the likelihood of a primary outcome when collecting promethazine (p = 0.19). Adjusted Cox analysis on the entire population indicated a further increased risk with more promethazine (HR for primary outcome among patients collecting ≥ 400 promethazine tablets/year=2.15, CI 1.94-2.38, p<0.0001).

Conclusions: Promethazine-treated patients with COPD had a concerning excess risk of a composite outcome of severe exacerbations and death from all causes compared to melatonin.

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