Diagnostic features of pulmonary hypertension in primary health care
https://doi.org/10.15829/3034-4123-2026-69
EDN: DGDNPE
Abstract
Aim. To identify the clinical, diagnostic, structural, functional, and hemodynamic parameters of the heart in patients with idiopathic pulmonary arterial hypertension (IPAH) and pulmonary hypertension (PH) associated with heart failure (HF) of ischemic origin to improve early diagnosis and differentiation of PH in primary health care, as well as to evaluate the practical applicability of a questionnaire as a primary screening tool for PH.
Material and methods. A total of 63 patients were examined. There were 32 patients with IPAH and 31 with HF-related PH. Following standard diagnostic methods were used: electrocardiography, echocardiography, chest X-ray, Holter monitoring, and laboratory tests. A specialized screening questionnaire developed by specialists at the Chazov National Medical Research Center of Cardiology was used for the early detection of PH. Final diagnosis was confirmed by transvenous right heart catheterization.
Results. Patients with IPAH were younger and predominantly female. This group of patients demonstrated more pronounced PH, hypertrophy and dilation of the right ventricles with preserved left ventricular function. In the group of PH with HF of ischemic origin, significant left heart structural changes were observed, including increased left ventricular size and volume, decreased ejection fraction, and increased pulmonary wedge pressure.
Conclusion. The study demonstrated significant clinical, anamnestic, and hemodynamic differences between various forms of PH, as well as the effectiveness of a screening questionnaire for the early detection of PH. This allows for optimized routing and improved prognosis for patients in primary care.
About the Authors
E. A. DevetyarovaRussian Federation
Elena A. Devetyarova
Bataysk; Rostov-on-Don
A. I. Chesnikova
Russian Federation
Anna I. Chesnikova
Rostov-on-Don
O. E. Kolomatskaya
Russian Federation
Olga E. Kolomatskaya
Rostov-on-Don
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What is already known about the subject?
- Diagnosis of pulmonary hypertension (PH) is difficult due to nonspecific symptoms and limited availability of transvenous cardiac catheterization.
- Idiopathic pulmonary arterial hypertension (IPAH) and PH associated with heart failure (HF) differ in their pathogenesis and treatment strategies.
What might this study add?
- IPAH is characterized by a younger patient age, a female predominance, and severe pulmonary artery hypertension with preserved left ventricular function, while PH associated with HF is associated with older age, male sex, and left heart structural changes.
- The screening questionnaire is informative for the early detection of PH even without echocardiographic data, allowing for a high probability of PH to be determined based solely on clinical symptoms, physical examination, and standard imaging techniques (electrocardiography, chest X-ray).
Review
For citations:
Devetyarova EA, Chesnikova AI, Kolomatskaya OE. Diagnostic features of pulmonary hypertension in primary health care. Primary Health Care (Russian Federation). 2026;3(1):6-15. (In Russ.) https://doi.org/10.15829/3034-4123-2026-69. EDN: DGDNPE
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