The healthcare burden of pulmonary alveolar proteinosis (PAP).

IF 3.4 2区 医学 Q2 GENETICS & HEREDITY
Elinor Lee, Ali Ataya, Cormac McCarthy, Erica Godart, John Cosenza, Alysse King, Brian Robinson, Tisha Wang
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引用次数: 0

Abstract

Introduction: Pulmonary alveolar proteinosis (PAP) is a rare lung syndrome characterized by the accumulation of surfactant in the alveoli. Using a longitudinal claims database, we compared measures of clinical and economic burden between a sample of diagnosed PAP patients and non-PAP matched controls.

Methods: PAP patients were identified leveraging IPM.ai's longitudinal U.S. claims database spanning January 1, 2009, through May 1, 2022. PAP patients were selected based on the presence of ICD-10: J84.01 or ICD-9: 516.0 in their claims history and were indexed for observation. An age, gender, and geographically matched control cohort was created (ratio of 1:4) for comparison. A third cohort, consisting of likely undiagnosed PAP patients, was identified using a machine learning model. The PAP and control cohorts were tracked longitudinally, depending on individual index dates, from January 1, 2018, through May 1, 2023. Inclusion criteria required evidence of continual claims activity 12 months prior to and after the index date, which reduced the total number of diagnosed PAP and control patients in the analysis. Demographics, comorbidities, procedures, medication use, annual healthcare resource utilization (HCRU), and costs were calculated for eligible PAP and control patients and were compared 12 months prior to, and 12 months after each patient's index date.

Results: After inclusion criteria were applied, 2312 confirmed PAP patients and 9247 matched controls were included in the analysis. Compared with matched controls, PAP patients had significantly higher rates of diagnosed conditions at baseline as defined by the Charlson Comorbidity Index (CCI). During the follow-up period, PAP patients had higher rates of diagnosed conditions, procedures, medication use, and cost-of-care compared with controls. PAP patients also had higher rates of emergency room visits (35% vs. 14%; P < 0.001), outpatient visits (87% vs. 56%; P < 0.001), inpatient visits (20% vs. 5%; P < 0.001) and had longer lengths of stay for inpatient hospitalizations (2.8 days vs. 0.56 days; P < 0.001), respectively.

Conclusion: This study represents the largest dataset of PAP patients and matched controls to be analyzed to date. Findings indicate that PAP patients have higher rates of diagnosed conditions, procedures, medication use, HCRU, and costs compared with non-PAP patients.

肺泡蛋白沉积症(PAP)的医疗负担。
肺泡蛋白沉积症(PAP)是一种罕见的肺部综合征,其特征是表面活性剂在肺泡内积聚。使用纵向索赔数据库,我们比较了诊断PAP患者和非PAP匹配对照之间的临床和经济负担。方法:利用IPM鉴别PAP患者。从2009年1月1日到2022年5月1日,ai的纵向美国索赔数据库。根据患者索赔史中是否存在icd - 10:j84.01或icd - 9:516.0,选择PAP患者进行索引观察。建立年龄、性别和地理位置匹配的对照队列(比例为1:4)进行比较。第三个队列,由可能未确诊的PAP患者组成,使用机器学习模型进行识别。根据个人指数日期,从2018年1月1日至2023年5月1日,对PAP和对照队列进行纵向跟踪。纳入标准需要在索引日期前后12个月的持续索赔活动证据,这减少了分析中诊断为PAP和对照患者的总数。计算符合条件的PAP患者和对照组患者的人口统计学、合并症、手术、药物使用、年度医疗资源利用率(HCRU)和费用,并比较每位患者指标日期前12个月和后12个月。结果:应用纳入标准后,2312例确诊PAP患者和9247例匹配对照纳入分析。根据Charlson合并症指数(CCI)的定义,与匹配的对照组相比,PAP患者的基线诊断率明显更高。在随访期间,与对照组相比,PAP患者的诊断状况、手术、药物使用和护理费用的比例更高。PAP患者也有更高的急诊室就诊率(35% vs. 14%;结论:该研究代表了迄今为止所分析的PAP患者和匹配对照的最大数据集。研究结果表明,与非PAP患者相比,PAP患者有更高的诊断条件、手术、药物使用、HCRU和费用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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