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首页> 外文期刊>Pragmatic and Observational Research >The CHRONICLE Study of US Adults with Subspecialist-Treated Severe Asthma: Objectives, Design, and Initial Results
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The CHRONICLE Study of US Adults with Subspecialist-Treated Severe Asthma: Objectives, Design, and Initial Results

机译:亚专业治疗严重哮喘的美国成年人的纪事研究:目标,设计和初始结果

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Background: Approximately 5– 10% of patients with asthma have severe disease. High-quality real-world studies are needed to identify areas for improved management. Objective: Aligned with the International Severe Asthma Registry, the CHRONICLE study (ClinicalTrials.gov: NCT03373045) was developed to address this need in the US. Study Design: Learnings from prior studies were applied to develop a real-world, prospective, noninterventional study of US patients with confirmed severe asthma who are treated by subspecialist physicians and require biologic or maintenance systemic immunosuppressant therapy or who are uncontrolled by high-dosage inhaled corticosteroids and additional controllers. Target enrollment is 4000 patients, with patient observation for ≥ 3 years. A geographically diverse sample of allergist/immunologist and pulmonologist sites approach all eligible patients under their care and report patient characteristics, treatment, and health outcomes every 6 months. Patients complete online surveys every 1– 6 months. Initial Results: From February 2018 to February 2019, 102 sites screened 1428 eligible patients; 936 patients enrolled. Study sites (40% allergist/immunologist, 42% pulmonologist, 18% both) were similar to other US asthma subspecialist samples. Enrolled patients were 67% female with median ages at enrollment and diagnosis of 55 (range: 18– 89) and 26 (0– 80) years, respectively. Median body mass index was 31 kg/m2 60% reported ≥ 1 exacerbation in the prior year and suboptimal symptom control. Conclusion: CHRONICLE will provide high-quality provider- and patient-reported data from a large, real-world cohort of US adults with subspecialist-treated severe asthma.
机译:背景:大约5-10%的哮喘患者具有严重疾病。需要高质量的现实研究,以确定改进管理的领域。目的:与国际严重哮喘登记处对齐,纪事研究(Clinicaltrials.gov:NCT03373045)是制定的,以解决美国的这种需求。研究设计:采用先前研究的学习,制定现实世界,前瞻性,对美国患者的真实哮喘患者进行了真实的严重哮喘患者,他们被亚专科医生治疗,需要生物学或维护全身免疫抑制剂治疗或由高剂量吸入的人不受控制皮质类固醇和额外的控制器。靶注册是4000名患者,患者观察≥3岁。地理位置不同的过敏症/免疫医生和肺病学家网站方法在其护理和报告每6个月内报告患者特征,治疗和健康结果的所有符合条件的患者。患者每1-6个月完成在线调查。初步结果:2018年2月至2019年2月,102个网站筛选了1428名符合条件的患者; 936名患者注册。研究网站(40%过敏症/免疫医生,42%肺病学,18%两者)与其他美国哮喘亚特色药物样本相似。注册的患者是67%的女性,入学和诊断中位数为55(范围:18-89)和26(0-80)年。中位体重指数为31公斤/平方米60%报告≥1年前的增生≥1个恶化和次优症状控制。结论:编年史将提供高质量的提供商和患者报告的来自美国大型成人队伍的大型现实世界队列的数据,其亚专业主义者治疗的严重哮喘。

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