:

Nerea Báez Gutiérrez1, Héctor Rodríguez Ramallo2, Elva María Mendoza-Zambrano3

  • 1Pharmacy Department, Hospital Universitario Virgen Macarena, Seville, Spain.

JMIR mHealth and uHealth
|October 30, 2024
PubMed
概括

肺高血压 (PH) 的移动健康应用程序正在出现,提供可接受的质量,但需要改进. 医疗保健专业人员的参与显著提高了应用程序的质量,强调了临床验证和以患者为中心的设计的必要性.

相关概念视频

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Pulmonary Hypertension: Classification and Pathogenesis

Pulmonary hypertension (PH) is a severe health condition in which the mean pulmonary arterial pressure increases to 25 mmHg or more, even when the body is at rest. This high pressure in the blood vessels that transport blood from the heart to the lungs can cause various symptoms, including shortness of breath, can lead to right heart failure, and significantly affect the overall quality of life.
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Treatment for Pulmonary Arterial Hypertension: Endothelin Receptor Antagonists

Endothelins (ETs) are potent vasoactive peptides critical in the human body's various physiological and pathological processes. One of the most promising therapeutic strategies for treating pulmonary arterial hypertension (PAH) involves counteracting the effects of these endothelins using a class of drugs known as endothelin receptor antagonists.
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