ArticleRespiration; international review of thoracic diseases2026
Nocturnal Hypoxaemia in PAH Patients Living at High Altitude Relocated to Low Altitude.
Article in Respiration; international review of thoracic diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
introductionPatients with pulmonary arterial hypertension (PAH) living at high altitudes experience exacerbated hypoxaemia. This study aimed to assess the effects of relocating PAH patients from high altitude (2,850 m) to sea level on nocturnal hypoxaemia, sleep-disordered breathing, and autonomic cardiovascular function.
methodsIn a repeated measures design, PAH patients underwent evaluations near their living altitude at 2,850 m and at sea level. The primary outcome was the change in mean nocturnal SpO
resultsA total of 8 patients (86% women) with a mean mean pulmonary artery pressure of 52 ± 17 mm Hg and PVR of 16.6 ± 8.8 Wood units were included. Relocation to sea level resulted in significant improvements in nocturnal hypoxaemia, with mean SpO
conclusionRelocation of PAH patients from high to low altitude led to significant improvements in nocturnal oxygenation and SDB, and enhanced parasympathetic activity, suggesting that short-term exposure to sea level may offer benefits for PAH-patients living at high altitude.
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