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Updated: May 22, 2025

Left Atrial Stenosis Induced Pulmonary Venous Arterialization and Group 2 Pulmonary Hypertension in Rat
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Published on: November 18, 2018

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与肺动脉高血压相关的社会成本 肺动脉高血压小组:使用链接国家注册表的研究

Barbro Kjellström1, Bodil Ivarsson2, Magnus Husberg3

  • 1Department of Clinical Sciences Lund Clinical Physiology and Skåne University Hospital, Lund University Lund Sweden.

Pulmonary circulation
|April 18, 2025
PubMed
概括

肺动脉高血压 (PAH) 显著增加了社会成本,特别是在诊断后. 自发性/遗传性PAH (IPAH/HPAH) 在诊断后承担最高的费用,主要是医疗费用.

关键词:
医疗保健资源利用率 医疗保健资源利用率国家登记处国家登记处生产力损失,生产力损失.肺高血压是一种肺高血压.

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Pulmonary Hypertension: Classification and Pathogenesis01:30

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.
There are various classifications for PH, each relating to different underlying causes and also...
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Treatment for Pulmonary Arterial Hypertension: Prostacyclin Receptor Agonists

Prostacyclin receptor agonists are a class of therapeutic agents integral to managing pulmonary arterial hypertension (PAH). These drugs operate by mimicking the action of prostaglandin I2, or PGI2, a naturally occurring compound in the body.
These agonists bind to the IPR receptor situated on the plasma membrane of the pulmonary artery smooth muscle cells. This binding triggers a cascade of reactions known as the GS-AC-cAMP-PKA pathway. This pathway results in the relaxation of smooth muscle...
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Treatment for Pulmonary Arterial Hypertension: Receptor Tyrosine Kinase Inhibitors and Calcium Channel Blockers

Receptor tyrosine kinase inhibitors (TKIs) and calcium channel blockers (CCBs) are two critical categories of drugs employed in the treatment of pulmonary artery hypertension (PAH). PAH is a disease that causes high blood pressure in the pulmonary arteries, resulting in chest pain, fatigue, and shortness of breath.
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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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Treatment for Pulmonary Arterial Hypertension: Oxygen Therapy for Respiratory Failure

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