Abstract

ObjectivePulmonary arterial hypertension (PAH) is a rare life-threatening and incurable disease. Although symptoms of depression and anxiety have been widely reported, these traits and associated factors have not been systematically assessed in Northwest China.MethodsA cross-sectional study was conducted between March 2020 and February 2021. 106 PAH patients in Northwest China were evaluated by Self-rating Anxiety Scale (SAS) and the Self Rating Depression Scale (SDS) questionnaire.ResultsOverall, the included patients had particularly high depressive symptoms (70.09%), while anxiety among them was 17.55%. Multivariate linear regression revealed that patients with lower age (p = 0.04), female (p < 0.01), smoking (p < 0.01), WHO functional class III/IV (p < 0.01), higher mean pulmonary hypertension (p < 0.01), lower left ventricular ejection fraction (p < 0.01), and lower 6-min walking distance (p < 0.01) had higher anxiety scores. Patients who lived in rural areas (p = 0.01), smoking (p < 0.01), WHO functional class III/IV (p < 0.01), higher mean pulmonary hypertension (p = 0.04), lower 6-min walking distance (p < 0.01), and college degree or above had higher depression scores (p = 0.02).ConclusionsMental health problems such as depression are common among patients with PAH in Northwest China. Patients' characteristics such as smoking status, WHO functional class, and 6-min walking distance were related to anxiety and depression scores. Thus, early detection of mental health problems such as depression and anxiety should be detected in PAH patients. Meanwhile, interventions against these problems should be used to improve such patients' mental status.

Highlights

  • Pulmonary hypertension (PH) is defined as mean pulmonary artery pressure (PAP) at rest of >25 mmHg [1]

  • According to WHO functional classifications (WHO FC), the majority (62.26%) of patients were classified as WHO FC III/IV

  • There was a lack of psychological support for pulmonary arterial hypertension (PAH) patients with depression in the present population, who have not received any type of intervention, and similar observations have been made in the study of Harzheim et al [24]

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Summary

Introduction

Pulmonary hypertension (PH) is defined as mean pulmonary artery pressure (PAP) at rest of >25 mmHg [1]. It is divided into five major categories [2]. One that is of particular clinical relevance is pulmonary arterial hypertension (PAH) [1]. An internationally registered epidemiological data on PAH showed that the prevalence of PAH was 15 cases per million adults. Even with PAH-specific drug treatment, there is yet no cure for it and survival for PAH patients remains poor [3]. Koudstaal et al.’s study showed that among newly diagnosed PAH cases, the 5-year survival rate was 61.2% [4]

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