Affiliation:
1. Department of Chemistry, Central University of Punjab, Punjab, India
2. Department of Chemistry, Banasthali Vidyapith Banasthali-304022, India
Abstract
Abstract:
In 1891, German doctor E. Romberg was the first to report PAH. It is widespread throughout the world, but it is particularly problematic in India and other developing countries. Pulmonary arterial hypertension (PAH) is characterised by an increase in pulmonary arterial pres-sure as well as the emergence of progressive symptoms, such as a loss of functional ability, short-ness of breath, and fatigue.
Blood flows from the right side of the heart to the lungs through the pulmonary arteries. Pulmonary arterial pressure refers to the pressure in the arteries of the lungs (PAH). It necessitates immediate treatment because high blood pressure in the lungs causes the right side of the heart to work much harder, increasing the risk of heart failure. This article aimed to provide brief information about the prevalence, pathology, classification, and different therapies of PAH.
Publisher
Bentham Science Publishers Ltd.
Subject
Pulmonary and Respiratory Medicine
Reference67 articles.
1. Matura L.A.; Carroll D.L.; Human responses to pulmonary arterial hypertension: review of the literature. J Cardiovasc Nurs 2010,25(5),420-427
2. Simonneau G.; Galiè N.; Rubin L.J.; Clinical classification of pulmonary hypertension. J Am Coll Cardiol 2004,43(12)(Suppl. S),5S-12S
3. Larrabee W.F.; Parker R.L.; Edwards J.E.; Pathology of intrapulmonary arteries and arterioles in mitral stenosis. Proc Staff Meet Mayo Clin 1949,24(12),316-326
4. Fishman A.P.; Respiratory gases in the regulation of the pulmonary circulation. Physiol Rev 1961,41(1),214-280
5. Fritts H.W.; Harris P.; Clauss R.H.; Odell J.E.; Cournand A.; The effect of acetylcholine on the human pulmonary circulation under normal and hypoxic conditions. J Clin Invest 1958,37(1),99-110
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