阿奇霉素治疗哮喘试点随机试验的次要结果。

PLoS clinical trials Pub Date : 2006-06-01 Epub Date: 2006-06-30 DOI:10.1371/journal.pctr.0010011
David L Hahn, Mary Beth Plane, Olaimatu S Mahdi, Gerald I Byrne
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引用次数: 0

摘要

目的:呼吸道病原体肺炎衣原体(C. pneumoniae)会引起急性和慢性肺部感染,并与哮喘有关。抗衣原体抗生素对哮喘的有效性证据有限。这项试点研究的主要目的是调查在大多数哮喘患者的诊疗环境中进行哮喘临床试验的可行性。次要目标是调查:(1) 阿奇霉素治疗是否会影响任何哮喘结果;(2) 肺炎双球菌血清学是否与结果有关。本报告介绍次要结果:随机、安慰剂对照、盲法(参与者、医生、研究人员、数据分析师)、分配隐藏的平行组临床试验:研究地点:美国四个州和加拿大一个省的社区医疗机构:干预措施:阿奇霉素(每周六次,每次 30 毫升):干预措施:阿奇霉素(每周六次)或相同的安慰剂,外加常规社区护理:瞻博网络哮喘生活质量问卷(Juniper AQLQ)、症状和用药从基线(治疗前)到治疗后 3 个月(随访)的变化;基线和随访时的肺炎球菌 IgG 和 IgA 抗体:结果:与安慰剂治疗相比,阿奇霉素治疗参与者的瞻博AQLQ提高了0.25(95%置信区间;-0.3,0.8)个单位,整体哮喘症状改善了0.68(0.1,1.3)个单位,每天使用的抢救性吸入器减少了0.59(-0.5,1.6)次。基线 IgA 抗体与随访时总体哮喘症状的恶化呈正相关(p = 0.04),但 IgG 抗体与之无关(p = 0.63)。高IgA参与者的哮喘症状总体改善率为28%,而低IgA参与者为12%(交互作用P = 0.27):结论:阿奇霉素不能改善瞻博网络AQLQ,但似乎能改善整体哮喘症状。以社区为基础的更大规模的抗衣原体抗生素治疗哮喘试验是有必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Secondary outcomes of a pilot randomized trial of azithromycin treatment for asthma.

Secondary outcomes of a pilot randomized trial of azithromycin treatment for asthma.

Secondary outcomes of a pilot randomized trial of azithromycin treatment for asthma.

Secondary outcomes of a pilot randomized trial of azithromycin treatment for asthma.

Objectives: The respiratory pathogen Chlamydia pneumoniae (C. pneumoniae) produces acute and chronic lung infections and is associated with asthma. Evidence for effectiveness of antichlamydial antibiotics in asthma is limited. The primary objective of this pilot study was to investigate the feasibility of performing an asthma clinical trial in practice settings where most asthma is encountered and managed. The secondary objectives were to investigate (1) whether azithromycin treatment would affect any asthma outcomes and (2) whether C. pneumoniae serology would be related to outcomes. This report presents the secondary results.

Design: Randomized, placebo-controlled, blinded (participants, physicians, study personnel, data analysts), allocation-concealed parallel group clinical trial.

Setting: Community-based health-care settings located in four states and one Canadian province.

Participants: Adults with stable, persistent asthma.

Interventions: Azithromycin (six weekly doses) or identical matching placebo, plus usual community care.

Outcome measures: Juniper Asthma Quality of Life Questionnaire (Juniper AQLQ), symptom, and medication changes from baseline (pretreatment) to 3 mo posttreatment (follow-up); C. pneumoniae IgG and IgA antibodies at baseline and follow-up.

Results: Juniper AQLQ improved by 0.25 (95% confidence interval; -0.3, 0.8) units, overall asthma symptoms improved by 0.68 (0.1, 1.3) units, and rescue inhaler use decreased by 0.59 (-0.5, 1.6) daily administrations in azithromycin-treated compared to placebo-treated participants. Baseline IgA antibodies were positively associated with worsening overall asthma symptoms at follow-up (p = 0.04), but IgG was not (p = 0.63). Overall asthma symptom improvement attributable to azithromycin was 28% in high IgA participants versus 12% in low IgA participants (p for interaction = 0.27).

Conclusions: Azithromycin did not improve Juniper AQLQ but appeared to improve overall asthma symptoms. Larger community-based trials of antichlamydial antibiotics for asthma are warranted.

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