Healthcare Resource Utilization Among Patients in England with Systemic Sclerosis-Associated Interstitial Lung Disease: A Retrospective Database Analysis
Autor: | Alicia Gayle, Margarida Alves, Christina Raabe, Francesco Del Galdo, Toby M. Maher, Nils Schoof, Prithwiraj Das, Deborah Clarke |
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Přispěvatelé: | National Institute for Health Research, British Lung Foundation |
Jazyk: | angličtina |
Rok vydání: | 2020 |
Předmět: |
Adult
Male medicine.medical_specialty Healthcare utilization Databases Factual Population Interstitial lung disease Disease behavioral disciplines and activities Interquartile range Internal medicine Observational study Medicine Electronic health records Humans Pharmacology (medical) CPRD education skin and connective tissue diseases General Clinical Medicine Original Research Aged Retrospective Studies Aged 80 and over education.field_of_study Scleroderma Systemic integumentary system business.industry Medical record Retrospective cohort study General Medicine Middle Aged Patient Acceptance of Health Care respiratory system medicine.disease SSc-ILD respiratory tract diseases England Systemic sclerosis Health Resources Female 1115 Pharmacology and Pharmaceutical Sciences Health Expenditures business Lung Diseases Interstitial Rare disease |
Zdroj: | Advances in Therapy |
ISSN: | 0741-238X |
Popis: | Introduction Systemic sclerosis-associated interstitial lung disease (SSc-ILD) places a substantial burden on patients and healthcare systems. The objectives of this study were to describe clinical characteristics and assess healthcare resource utilization and costs of patients with SSc-ILD in England, compared with patients with non-pulmonary organ involvement related to SSc (SSc-OOI). Methods This population-based retrospective study used data from the Clinical Practice Research Datalink linked to Hospital Episode Statistics. Data were extracted from medical records dated January 1, 2005 to March 31, 2016. Patients with SSc were identified and placed in subgroups based on organ involvement: SSc-ILD, SSc-OOI, and both (SSc-ILD-OOI). Patients with SSc-ILD-OOI were included in both the SSc-ILD and SSc-OOI subgroups. All-cause healthcare costs, excluding medication costs, were calculated to 2016 British pounds sterling (£). Results This study included 675 patients with SSc: 174 (26%) had neither ILD nor other organ involvement (OOI); 127 (19%) had SSc-ILD; 477 (71%) had SSc-OOI; 103 (15%) had SSc-ILD-OOI. Age-weighted median [interquartile range (IQR)] annual healthcare costs per patient were: £1496 (£664–£2817) in SSc only; £6375 (£3451–£15,041) in SSc-ILD; £4084 (£1454–£10,105) in SSc-OOI; £6632 (£4023–£17,009) in SSc-ILD-OOI. In multivariate analysis, older age at diagnosis, diagnosis of anemia, and number of comorbid diseases were associated with higher yearly healthcare costs. Conclusion The annual healthcare cost for patients with SSc-ILD is substantial, and higher than that of patients with SSc-OOI or SSc only. These results quantify the economic burden of SSc-ILD in a real-world setting, and highlight the need for treatment of this disease. Electronic supplementary material The online version of this article (10.1007/s12325-020-01330-0) contains supplementary material, which is available to authorized users. Plain Language Summary SSc is a rare disease that causes fibrosis, or thickening, of the skin. In some patients, SSc can also affect the lungs (‘SSc-ILD’) or other organs, e.g., the heart (‘SSc-OOI’). Patients with SSc-ILD typically have high healthcare costs; however, it is not clear how costs for SSc-ILD compare with those for SSc-OOI. To investigate this, we evaluated the costs associated with SSc-ILD and compared them with those for SSc only or SSc-OOI. In this England-based study, the annual healthcare costs for patients with SSc-ILD were approximately 50% higher than for those without lung disease (SSc only) or SSc-OOI. These results highlight the importance of promptly diagnosing and treating patients with lung fibrosis complicating SSc. Electronic supplementary material The online version of this article (10.1007/s12325-020-01330-0) contains supplementary material, which is available to authorized users. |
Databáze: | OpenAIRE |
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