The hospitalization rate for patients with pulmonary hypertension (PH) and interstitial lung disease (ILD) doubled over a 2-year period, and total health care costs more than doubled over the same period.
A retrospective cohort analysis that analyzed records for 122 patients with pulmonary hypertension due to interstitial lung disease (PH-ILD) over a 2-year period bisected by their first pulmonary hypertension (PH) diagnosis found that all-cause hospitalizations rose from 29.5% of patients pre-index to 59.0% of patients post index, according to a study in BMC Pulmonary Medicine.1
Mean (SD) all-cause health care costs climbed to $108,387 ($190,673) post index compared with $43,201 ($98,604) pre-index (P < .0001), largely due to hospitalizations, the authors stated. They also saw approximate 150% increases in median health care costs of $20,732 to $50,843.
“This change was driven primarily by higher rates of inpatient care, more outpatient visits, and increased prescription drug use,” the authors stated.
Other measures also showed an increase over the 4-year period: intensive care unit (ICU) stays (6.6% vs 17.2%), mean inpatient visits (0.5 to 1.1), length of stay (5.4 vs 7.5 days), bed days (2.5 to 8), ICU days (3.8 vs 7), and outpatient visits (24.5 to 32.9).
Hospitalization costs increased from a mean of $13,133 ($28,752) to $63,218 ($142,142) over the period (P < .0001), and outpatient costs from $16,150 ($75,639) to $25,604 ($93,964) (P < .0001).
Hospitalizations among patients with comorbid pulmonary hypertension and interstitial lung disease more than doubled over a 2-year period in this analysis | Image Credit: meeboonstudio-stock.adobe.com
Most patients (99.2%) were recorded as making outpatient visits during the pre- and postindex periods. Slightly more than a third of patients visited the emergency department (ED) in both the pre- and postindex periods (37.7% vs 34.4%), and the majority of patients had a doctor visit during these periods (93.4% vs 94.3%). The mean for overall outpatient visits was significantly higher post index relative to preindex (32.9 vs 24.5).
Patients were indexed according to their first claim on a PH diagnosis. Researchers then compared data 12 months prior to index date with 12 months post index.
The mean age of patients, who were all adults, was 63.7 years; 64.8% were female; and 54.9% had commercial insurance. Patients’ most common comorbidities were chronic pulmonary disease (94.3%), diabetes (36.1%), and rheumatic disease (34.4%).
Patients largely stayed on the same medications pre- and post index: corticosteroids (43.4% vs 53.5%), calcium channel blockers (25.4% vs 36.9%), and oxygen (12.3% vs 25.4%). Data were taken from the Truven Health MarketScan Commercial Claims and Encounters Database and Medicare Supplemental Database. Patients with non-ILD, PH-associated conditions were excluded from the study.
To calculate total health care costs, the researchers included medical and prescription costs paid by both the health plan and patient (copayments, coinsurance, deductibles).
Roughly 5% of patients seeing a doctor for the first time due to pulmonary fibrosis may also suffer from PH, and some studies have shown that about 15% to 50% of patients with IPF may have associated PH, according to the Pulmonary Fibrosis Foundation.2
“Patients with ILD can develop PH over time. The presence of PH in patients with ILD can lead to worse survival compared to ILD alone, although more information is needed to better understand the impact of PH on ILD patient,” Benjamin Wu, PharmD, MS, coauthor of the study and a health economics and outcomes researcher at United Therapeutics Corporation, wrote in an email. “Our study showed that PH-ILD leads to major increases in hospitalizations and healthcare costs. Timely management and treatment of patients with PH-ILD is needed and could help mitigate the detrimental clinical and economic consequences.”
References
1. Heresi G, Dean B, Wu B, et al. Burden of illness in patients with pulmonary hypertension due to interstitial lung disease: a real-world analysis. BMC Pulm Med. 2024;24(1):335. doi:10.1186/s12890-024-03141-3
2. Pulmonary hypertension related to ILD (for patients). Pulmonary Fibrosis Foundation. Accessed July 17, 2024. https://www.pulmonaryfibrosis.org/researchers-healthcare-providers/clinical-resources/position-statements/pulmonary-hypertension-related-to-ild-for-patients
The Role of Transplant in the Era of Novel MM Therapies: Harsh Parmar, MD
May 17th 2025Novel therapies for multiple myeloma (MM), including chimeric antigen receptor T-cell and bispecific antibodies, extend lives but raise concerns about treatment costs and adherence, and they haven't replaced stem cell transplantation, Harsh Parmar, MD, of Hackensack University Medical Center, explains.
Read More
Inside the Center's MDD Value Model and Its Use of Dynamic Pricing
May 13th 2025Larragem Raines, MS, of the Center for Innovation & Value Research, discusses the organization's major depressive disorder (MDD) open-source value model, dynamic pricing, and the future role of artificial intelligence in care.
Listen
Dual Therapy Appears to Benefit Patients With Pulmonary Fibrosis, Pulmonary Hypertension
May 15th 2025The combination of antifibrotic therapy and pulmonary vasodilator therapy improved transplant-free survival but had no significant impact on exercise capacity in pulmonary fibrosis and pulmonary hypertension.
Read More
RFK Jr Claims HHS Has Not Fired Working Scientists, Canceled Lifesaving Research
May 15th 2025Robert F. Kennedy Jr’s congressional hearing featured numerous statements from the secretary of HHS, including denouncing claims of cutting down the HHS and the National Institutes of Health.
Read More
Navigation and Clinician Payment Investments Enhance Colorectal Cancer Screening Benefits
May 15th 2025Investing in patient navigation and clinician incentives ensures colorectal cancer screening completion, improves early detection, reduces disparities, achieves cost savings, and advances population health for all stakeholders.
Read More