ArticleCureus2025
Burden of Pulmonary Arterial Hypertension (PAH) on Patients Admitted for Asthma: A Nationwide Analysis, 2016-2020.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Chronic Mixed-Allergen Exposure Induces Pulmonary Arterial Remodeling and Vascular Dysfunction in Mice.American journal of physiology. Lung cellular and molecular physiology · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background Pulmonary arterial hypertension (PAH) is known to impact other pulmonary disease outcomes, but there is a lack of data showing the degree of its impact. This study aims to elucidate the burden that PAH brings to patients admitted due to asthma. Methods The National Inpatient Sample (NIS) Database 2016-2020 was used to identify patients admitted due to asthma exacerbation. Patients admitted with a primary diagnosis of asthma, with or without a secondary diagnosis of PAH, were identified using International Classification of Diseases, 10th Edition (ICD-10) codes. PAH was classified using ICD-10 codes, specifically Group 3 PAH. The primary outcome was all-cause in-hospital mortality. Secondary outcomes were length of stay, resource utilization, and the necessity for endotracheal intubation. STATA v.13 (StataCorp LLC, College Station, TX, USA) was used for univariate and multivariate analysis. Data were considered statistically significant at p < 0.05. Results From 2016 to 2020, 491,990 patients were admitted due to asthma, and 7,860 had PAH. Patients with asthma and PAH had a 226% higher chance of dying during the index admission (OR 2.26; 95% CI 1.27-4.03; p = 0.006), an additional 0.75 days of hospital stay (regression coefficient 0.75; 95% CI 0.54-0.95; p < 0.001), and an average of $11,558.41 more spent per hospital stay (regression coefficient 11,558.41; 95% CI 8,657.33-14,459.49; p < 0.001). These patients had no statistically significant difference in endotracheal intubation rates (OR 1.69; 95% CI 0.80-1.94; p = 0.42). Discussion Asthma patients with PAH experience higher all-cause in-hospital mortality compared to those with asthma alone. These results highlight the increased risk associated with the coexistence of PAH and asthma, potentially due to the added hemodynamic burden imposed by PAH, which exacerbates respiratory and cardiovascular compromise. Activation of the transcription factor nuclear factor of activated T cells (NFAT) is an important marker known to link PAH and asthma. Due to its activation in both diseases, it may serve as a critical pathway for developing more effective therapeutic strategies targeting both conditions. There is also some research suggesting that increased neutrophils in asthma are correlated with PAH. Some limitations of using the NIS database are that it is subject to coding errors, misclassification, and variability across institutions, potentially affecting diagnostic and procedural accuracy. Conclusion PAH significantly impacts in-hospital outcomes in patients admitted due to asthma; thus, physicians should be aware of this difference. Future studies are needed to differentiate PAH patients by severity and to verify whether PAH treatment reverses this impact.
Indexed as
Identifiers
What Socratic holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.