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患者は50歳,男性.原発性肺高血圧症(primary pulmonary hypertension:PPH)と診断後,外来治療として,prostaglandin E1の持続経口投与および在宅酸素療法を中心に行ったが,約3年間の経過後,肺循環動態の悪化を来し,さらに右心不全を伴ってきたため入院.心不全の治療を行うと同時に,安定したprostaglandin I2誘導体であるベラプロストナトリウム(BPS)を60μg/日より経口投与開始し,3カ月後180μg/日に増量後,肺動脈圧と肺血管抵抗はともに低下し,肺循環動態の改善を認めた.これは,BPSの強力な血管拡張効果,血小板凝固抑制効果,血小板粘着抑制効果および抗血栓効果によるものと思われる.今後,本薬はPPHの有効な治療薬の1つとなり得ると思われる.
The patient is a 50-year-old male. In these 2.6 years, he has been under oral prostaglandin E1 therapy and home oxygen therapy at our outpatient clinic with a diagnosis of primary pulmonary hypertension (PPH). He was admitted to our hospital because of the aggra-vation of pulmonary hemodynamics. Oral administra-tion of beraprostsodium (BPS), a stable prostaglandin I2 derivative, was given at the initial dose of 60μg/dayand final increase dose of 180μg/day. Both the arterial pressure and pulmonary arterialar resistance were de-creased. This improvement is considered to be due to its vasodilative, antiplatelet activity, antiplatelet and antithrombotic actions of BPS. It was suggested that BPS effectively suppress the progress of the PPH.
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