Hospitalization Among Pulmonary Arterial Hypertension Patients With and Without Connective Tissue Disease Comorbidities Prescribed Oral Selexipag
Title: | Hospitalization Among Pulmonary Arterial Hypertension Patients With and Without Connective Tissue Disease Comorbidities Prescribed Oral Selexipag |
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Authors: | Yuen Tsang, Risho Singh, Sumit Verma, Sumeet Panjabi |
Source: | Rheumatology and Therapy, Vol 10, Iss 3, Pp 741-756 (2023) |
Publisher Information: | Adis, Springer Healthcare, 2023. |
Publication Year: | 2023 |
Collection: | LCC:Diseases of the musculoskeletal system |
Subject Terms: | Pulmonary arterial hypertension, Selexipag, Connective tissue disease, Health care costs, Diseases of the musculoskeletal system, RC925-935 |
More Details: | Abstract Introduction Patients with connective tissue disorders (CTD) and pulmonary arterial hypertension (PAH) have a poorer prognosis than those with other PAH etiologies. This study assessed the impact of CTD on healthcare outcomes among PAH patients with and without CTD comorbidities that were treated with oral selexipag. Methods The study utilized Optum’s de-identified Clinformatics® Data Mart Database (2007–2021) from January 1, 2014 to June 30, 2019, and identified patients with PAH without CTD and PAH with CTD treated with oral selexipag. Patients had ≥ 12-month baseline period with no requirement for a minimum follow-up period. Patients were followed until any of the following events: discontinuation of oral selexipag, or health plan disenrollment, or death, or presence of a diagnosis claim for CTEPH, or study end date, whichever occurred first. PAH-related hospitalizations, PAH disease progression, and healthcare utilizations and costs were assessed in the follow-up period. The Cox proportional hazards model was used to evaluate the time to hospitalization and generalized linear models were used to examine healthcare costs and utilization between the two cohorts. Results In the analysis, 237 PAH without CTD, and 80 PAH patients with CTD comorbidities prescribed oral selexipag were included. The PAH without CTD comorbidities cohort was older (65 vs. 63 years old), had proportionately less females (72 vs. 83%), and higher comorbidity burden than PAH with CTD comorbidities (mean CCI index 3 vs. 2). After adjusting for potential confounders, the risk for PAH-related hospitalization (hazard ratio (HR) 1.13, p value 0.641), all-cause hospitalization (HR 1.09, p value: 0.765), and PAH disease progression (HR 1.14, p value 0.522) between the two cohorts were similar. After adjusting for baseline demographic and clinical characteristics, PAH with CTD comorbidities incurred higher total mean all-cause PAH-related medical care costs compared to PAH without CTD comorbidities. Conclusions In this real-world study, the risk of hospitalization and PAH disease progression were similar between the two cohorts who received oral selexipag. The results from this study corroborate findings of the GRIPHON post hoc analysis of PAH-associated CTD patients and support oral selexipag use in PAH-CTD patients. |
Document Type: | article |
File Description: | electronic resource |
Language: | English |
ISSN: | 2198-6576 2198-6584 |
Relation: | https://doaj.org/toc/2198-6576; https://doaj.org/toc/2198-6584 |
DOI: | 10.1007/s40744-023-00547-z |
Access URL: | https://doaj.org/article/b3ae782811fe4d53aefb60b787e2da4c |
Accession Number: | edsdoj.b3ae782811fe4d53aefb60b787e2da4c |
Database: | Directory of Open Access Journals |
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Items | – Name: Title Label: Title Group: Ti Data: Hospitalization Among Pulmonary Arterial Hypertension Patients With and Without Connective Tissue Disease Comorbidities Prescribed Oral Selexipag – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Yuen+Tsang%22">Yuen Tsang</searchLink><br /><searchLink fieldCode="AR" term="%22Risho+Singh%22">Risho Singh</searchLink><br /><searchLink fieldCode="AR" term="%22Sumit+Verma%22">Sumit Verma</searchLink><br /><searchLink fieldCode="AR" term="%22Sumeet+Panjabi%22">Sumeet Panjabi</searchLink> – Name: TitleSource Label: Source Group: Src Data: Rheumatology and Therapy, Vol 10, Iss 3, Pp 741-756 (2023) – Name: Publisher Label: Publisher Information Group: PubInfo Data: Adis, Springer Healthcare, 2023. – Name: DatePubCY Label: Publication Year Group: Date Data: 2023 – Name: Subset Label: Collection Group: HoldingsInfo Data: LCC:Diseases of the musculoskeletal system – Name: Subject Label: Subject Terms Group: Su Data: <searchLink fieldCode="DE" term="%22Pulmonary+arterial+hypertension%22">Pulmonary arterial hypertension</searchLink><br /><searchLink fieldCode="DE" term="%22Selexipag%22">Selexipag</searchLink><br /><searchLink fieldCode="DE" term="%22Connective+tissue+disease%22">Connective tissue disease</searchLink><br /><searchLink fieldCode="DE" term="%22Health+care+costs%22">Health care costs</searchLink><br /><searchLink fieldCode="DE" term="%22Diseases+of+the+musculoskeletal+system%22">Diseases of the musculoskeletal system</searchLink><br /><searchLink fieldCode="DE" term="%22RC925-935%22">RC925-935</searchLink> – Name: Abstract Label: Description Group: Ab Data: Abstract Introduction Patients with connective tissue disorders (CTD) and pulmonary arterial hypertension (PAH) have a poorer prognosis than those with other PAH etiologies. This study assessed the impact of CTD on healthcare outcomes among PAH patients with and without CTD comorbidities that were treated with oral selexipag. Methods The study utilized Optum’s de-identified Clinformatics® Data Mart Database (2007–2021) from January 1, 2014 to June 30, 2019, and identified patients with PAH without CTD and PAH with CTD treated with oral selexipag. Patients had ≥ 12-month baseline period with no requirement for a minimum follow-up period. Patients were followed until any of the following events: discontinuation of oral selexipag, or health plan disenrollment, or death, or presence of a diagnosis claim for CTEPH, or study end date, whichever occurred first. PAH-related hospitalizations, PAH disease progression, and healthcare utilizations and costs were assessed in the follow-up period. The Cox proportional hazards model was used to evaluate the time to hospitalization and generalized linear models were used to examine healthcare costs and utilization between the two cohorts. Results In the analysis, 237 PAH without CTD, and 80 PAH patients with CTD comorbidities prescribed oral selexipag were included. The PAH without CTD comorbidities cohort was older (65 vs. 63 years old), had proportionately less females (72 vs. 83%), and higher comorbidity burden than PAH with CTD comorbidities (mean CCI index 3 vs. 2). After adjusting for potential confounders, the risk for PAH-related hospitalization (hazard ratio (HR) 1.13, p value 0.641), all-cause hospitalization (HR 1.09, p value: 0.765), and PAH disease progression (HR 1.14, p value 0.522) between the two cohorts were similar. After adjusting for baseline demographic and clinical characteristics, PAH with CTD comorbidities incurred higher total mean all-cause PAH-related medical care costs compared to PAH without CTD comorbidities. Conclusions In this real-world study, the risk of hospitalization and PAH disease progression were similar between the two cohorts who received oral selexipag. The results from this study corroborate findings of the GRIPHON post hoc analysis of PAH-associated CTD patients and support oral selexipag use in PAH-CTD patients. – Name: TypeDocument Label: Document Type Group: TypDoc Data: article – Name: Format Label: File Description Group: SrcInfo Data: electronic resource – Name: Language Label: Language Group: Lang Data: English – Name: ISSN Label: ISSN Group: ISSN Data: 2198-6576<br />2198-6584 – Name: NoteTitleSource Label: Relation Group: SrcInfo Data: https://doaj.org/toc/2198-6576; https://doaj.org/toc/2198-6584 – Name: DOI Label: DOI Group: ID Data: 10.1007/s40744-023-00547-z – Name: URL Label: Access URL Group: URL Data: <link linkTarget="URL" linkTerm="https://doaj.org/article/b3ae782811fe4d53aefb60b787e2da4c" linkWindow="_blank">https://doaj.org/article/b3ae782811fe4d53aefb60b787e2da4c</link> – Name: AN Label: Accession Number Group: ID Data: edsdoj.b3ae782811fe4d53aefb60b787e2da4c |
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RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1007/s40744-023-00547-z Languages: – Text: English PhysicalDescription: Pagination: PageCount: 16 StartPage: 741 Subjects: – SubjectFull: Pulmonary arterial hypertension Type: general – SubjectFull: Selexipag Type: general – SubjectFull: Connective tissue disease Type: general – SubjectFull: Health care costs Type: general – SubjectFull: Diseases of the musculoskeletal system Type: general – SubjectFull: RC925-935 Type: general Titles: – TitleFull: Hospitalization Among Pulmonary Arterial Hypertension Patients With and Without Connective Tissue Disease Comorbidities Prescribed Oral Selexipag Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Yuen Tsang – PersonEntity: Name: NameFull: Risho Singh – PersonEntity: Name: NameFull: Sumit Verma – PersonEntity: Name: NameFull: Sumeet Panjabi IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 03 Type: published Y: 2023 Identifiers: – Type: issn-print Value: 21986576 – Type: issn-print Value: 21986584 Numbering: – Type: volume Value: 10 – Type: issue Value: 3 Titles: – TitleFull: Rheumatology and Therapy Type: main |
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