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. 2023 Jan 1;13(1):e12190.
doi: 10.1002/pul2.12190. eCollection 2023 Jan.

Societal costs associated with pulmonary arterial hypertension: A study utilizing linked national registries

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Societal costs associated with pulmonary arterial hypertension: A study utilizing linked national registries

Hannes Runheim et al. Pulm Circ. .

Abstract

Pulmonary arterial hypertension (PAH) is a progressive disease with no cure. Healthcare resource utilization (HCRU; hospitalization, outpatient visits, and drug utilization) before diagnosis and productivity loss (sick leave and disability pension) before and after PAH diagnosis are not well known. By linking several Swedish national databases, this study have estimated the societal costs in a national PAH cohort (n = 749, diagnosed with PAH in 2008-2019) 5 years before and 5 years after diagnosis and compared to an age, sex, and geographically matched control group (n = 3745, 1:5 match). HCRU and productivity loss were estimated per patient per year. The PAH group had significantly higher HCRU and productivity loss compared to the control group starting already 3 and 5 years before diagnosis, respectively. HCRU peaked the year after diagnosis in the PAH group with hospitalizations (mean ± standard deviation; 2.0 ± 0.1 vs. 0.2 ± 0.0), outpatient visits (5.3 ± 0.3 vs. 0.9 ± 0.1), and days on sick leave (130 ± 10 vs. 13 ± 1) significantly higher compared to controls. Total costs during the entire 10-year period were six times higher for the PAH group than the control group. In the 5 years before diagnosis the higher costs were driven by productivity loss (76%) and hospitalizations (15%), while the 5 years after diagnosis the main cost drivers were drugs (63%), hospitalizations (16%), and productivity loss (16%). In conclusion, PAH was associated with large societal costs due to high HCRU and productivity loss, starting several years before diagnosis. The economic and clinical burden of PAH suggests that strategies for earlier diagnosis and more effective treatments are warranted.

Keywords: healthcare resource utilization; national registry; productivity loss; pulmonary hypertension.

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Conflict of interest statement

Amélie Beaudet and Nadia Pillai are employees of Actelion Pharmaceuticals, a Janssen Pharmaceutical Company of Johnson & Johnson, Allschwil, Switzerland. The remaining authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Healthcare resource utilization by hospitalizations. (a) Mean number of hospitalizations per person and year (analysis includes only surviving patients with complete follow‐up data per year). (b) Proportion with at least one hospitalization per year. (c) Mean number of days spent hospitalized per person and year. ***p < 0.001; **p < 0.01; *p < 0.05.
Figure 2
Figure 2
Healthcare resource utilization by outpatient visits and dispensed drugs (DDD). (a) Mean number of outpatient visits per person and year (analysis includes only surviving patients with complete follow‐up data per year). (b) Drug utilization, DDD of drugs per person and year. ***p < 0.001; **p < 0.01; *p < 0.05. DDD, defined daily dose.
Figure 3
Figure 3
Productivity loss for individuals eligible for sick leave or disability pension, that is, not yet receiving age pension as main income. (a) Sick leave, mean days per person and year (full time equivalents). (b) Disability pension, mean days per person and year (full time equivalents). ***p < 0.001; **p < 0.01; *p < 0.05.
Figure 4
Figure 4
Overall survival for the PAH group and their matched control group by Kaplan−Meier estimates for 5 years with follow‐up from index date censored at the date of last contact or death. PAH, pulmonary arterial hypertension.

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