Development and validation of a claims-based model to identify patients at risk of chronic thromboembolic pulmonary hypertension following acute pulmonary embolism

被引:2
作者
Kanwar, Manreet K. [1 ]
Cole, Michele [2 ]
Gauthier-Loiselle, Marjolaine [3 ]
Manceur, Ameur M. [3 ]
Tsang, Yuen [2 ]
Lefebvre, Patrick [3 ]
Panjabi, Sumeet [2 ]
Benza, Raymond L. [4 ]
机构
[1] Allegheny Hlth Network, Cardiovasc Inst, Pittsburgh, PA USA
[2] Actelion Pharmaceut US Inc, San Francisco, CA USA
[3] Anal Grp Inc, Montreal, PQ, Canada
[4] Ohio State Univ, Wexner Med Ctr, Div Cardiovasc Dis, Columbus, OH 43210 USA
关键词
Chronic thromboembolic pulmonary hypertension; pulmonary embolism; predictive risk model; validation; health insurance claims; SCORE; PREVALENCE; CTEPH;
D O I
10.1080/03007995.2021.1947215
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective Chronic thromboembolic pulmonary hypertension (CTEPH) is a rare disease that often follows pulmonary embolism (PE). Screening for CTEPH is challenging, often delaying diagnosis and worsening prognosis. Predictive risk models for CTEPH could help identify at-risk patients, but existing models require multiple clinical inputs. We developed and validated a predictive risk model for CTEPH using health insurance claims that can be used by payers/quality-of-care organizations to screen patients post-PE. Methods Adult patients newly diagnosed with acute PE (index date) were identified from the Optum De-identified Clinformatics Extended DataMart (January 2007-March 2018; development set) and IBM MarketScan (January 2008-June 2019; validation set) databases. Predictors were identified 12 months before or on the index PE. Risk of "likely CTEPH" was assessed post-PE based on CTEPH-related diagnoses and procedures since the CTEPH diagnosis code (ICD-10-CM: I27.24) was not available until 1 October 2017. Stepwise variable selection was used to build the model using the development set; model validation was subsequently conducted using the validation set. Results The development set included 93,428 patients, of whom 11,878 (12.7%) developed likely CTEPH. Older age (odds ratios [OR] = 1.16-1.49), female (OR = 1.09), unprovoked PE (i.e. without thrombotic factors; OR = 1.14), hypertension (OR = 1.07), osteoarthritis (OR = 1.08), diabetes (OR = 1.07), chronic obstructive pulmonary disease (OR = 1.11), obesity (OR = 1.21) were associated with higher odds of likely CTEPH, and oral anticoagulants with lower odds (OR= 0.50, all p < .01). C-statistic was 0.77 in the development and validation sets. Conclusion A claims-based risk model reliably predicted the risk of CTEPH post-PE and could be used to identify high-risk patients who may benefit from focused monitoring.
引用
收藏
页码:1483 / 1491
页数:9
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