Experiencing chronic cough symptoms for 3 years is associated with increased rates of healthcare resource use and higher healthcare costs in the United States compared to resolved chronic cough.

IF 2.4 4区 医学 Q1 MEDICINE, GENERAL & INTERNAL Current Medical Research and Opinion Pub Date : 2025-01-15 DOI:10.1080/03007995.2024.2433252
Xuehua Ke, Helen Ding, Yezhou Sun, Daisuke Goto, Prajakta Waghmare, Mingyue Li
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Abstract

Objective: Chronic cough (CC) symptoms can persist as refractory or unexplained CC (RCC). We sought to characterize the clinical and economic burden of RCC.

Methods: In this retrospective US cohort study using data from Optum's de-identified CDM Database (01/2015-03/2022), CC was identified as ≥1 CC diagnosis or ≥3 cough events (with ≥8 weeks and ≤120 days between the first and third events and ≥3 weeks between any two events). The index date was set as the earliest date of meeting the CC definition. The baseline period was defined as the 364 days prior to and including the index date. Adults with CC at baseline who met CC requirements (≥1 CC diagnosis, or ≥2 cough events occurring ≥8 weeks but ≤120 days apart) in both follow-up year 2 and follow-up year 3 were defined as having "3-year chronic cough" (3YCC), a proxy measure of RCC, and compared to adults with CC at baseline who did not meet CC requirements in follow-up years 2 and 3 (non-3YCC). A propensity score weighting approach was used to adjust for baseline differences between the 3YCC and non-3YCC groups to compare clinical characteristics and healthcare resource use and costs in the two groups during the follow-up period.

Results: At baseline, the 3YCC group (N = 3,338) had significantly more comorbidities and higher all-cause healthcare resource use and costs than the non-3YCC group (N = 43,122) in unweighted analyses. After weighting, the groups (N = 3,338 with 3YCC and N = 3,145 without) were compared during a 3-year follow-up period. The 3YCC group had significantly more comorbidities, higher levels of all-cause healthcare resource use, and higher all-cause healthcare costs during the follow-up period compared to the non-3YCC group, after adjusting for baseline differences. For example, the mean total healthcare costs (in 2022 US dollars) were significantly higher among the 3YCC group than the non-3YCC group in each follow-up year, at $49,454 versus $42,144 in follow-up year 1, $49,339 versus $36,939 in follow-up year 2, and $51,737 versus $36,503 in follow-up year 3 (p <.001 for each comparison).

Conclusions: After adjusting for baseline differences, persistent symptoms of CC were associated with significantly higher comorbidity, healthcare resource use, and healthcare costs compared to CC that resolved. Effective treatments for RCC would thus be expected to result in improved health as well as substantial healthcare cost offsets.

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在美国,与缓解的慢性咳嗽相比,持续 3 年的慢性咳嗽症状与更高的医疗资源使用率和更高的医疗费用有关。
目的:慢性咳嗽(CC)症状可持续存在,表现为难治性或原因不明的慢性咳嗽(RCC)。我们试图描述 RCC 的临床和经济负担:在这项回顾性美国队列研究中,我们使用了 Optum 的去标识 CDM 数据库(01/2015-03/2022)中的数据,CC 被认定为≥1 次 CC 诊断或≥3 次咳嗽事件(第一次和第三次咳嗽事件之间的间隔时间≥8 周且≤120 天,任何两次咳嗽事件之间的间隔时间≥3 周)。指数日期定为符合 CC 定义的最早日期。基线期定义为指数日期之前(包括指数日期)的 364 天。在随访第二年和随访第三年均符合CC要求(≥1次CC诊断,或≥2次咳嗽事件发生时间间隔≥8周但不超过120天)的基线期CC成人被定义为 "3年慢性咳嗽"(3YCC),这是RCC的替代指标,并与在随访第二年和第三年不符合CC要求的基线期CC成人(非3YCC)进行比较。采用倾向得分加权法调整3YCC组和非3YCC组之间的基线差异,比较两组在随访期间的临床特征、医疗资源使用情况和成本:在未加权分析中,3YCC组(N = 3,338)的基线合并症明显多于非3YCC组(N = 43,122),全因医疗资源使用量和成本也高于非3YCC组。经过加权后,两组(3YCC 组 3,338 人,无 3YCC 组 3,145 人)在 3 年随访期内进行了比较。在调整基线差异后,3YCC 组与未 3YCC 组相比,在随访期间有明显更多的合并症、更高水平的全因医疗资源使用和更高的全因医疗费用。例如,在每个随访年,3YCC组的平均医疗总费用(以2022年美元计算)都显著高于非3YCC组,随访第1年为49,454美元对42,144美元,随访第2年为49,339美元对36,939美元,随访第3年为51,737美元对36,503美元(各比较的P0.001):在调整基线差异后,与症状缓解的CC相比,CC的持续症状与更高的合并症、医疗资源使用和医疗费用相关。因此,RCC的有效治疗有望改善患者的健康状况,并减少大量医疗费用。
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来源期刊
Current Medical Research and Opinion
Current Medical Research and Opinion 医学-医学:内科
CiteScore
4.40
自引率
4.30%
发文量
247
审稿时长
3-8 weeks
期刊介绍: Current Medical Research and Opinion is a MEDLINE-indexed, peer-reviewed, international journal for the rapid publication of original research on new and existing drugs and therapies, Phase II-IV studies, and post-marketing investigations. Equivalence, safety and efficacy/effectiveness studies are especially encouraged. Preclinical, Phase I, pharmacoeconomic, outcomes and quality of life studies may also be considered if there is clear clinical relevance
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