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Additional effects of bosentan in patients with idiopathic pulmonary arterial hypertension already treated with high-dose epoprostenol.
Author: AkagiSatoshi, DanKazuhiro, FujimotoYoshihisa, HisamatsuKenichi, IkedaEtsuko, MatsubaraHiromi, MiyajiKatsumasa, MunemasaMitsuru, OheTohru, TokunagaNaoto
Original Abstract of the Article :
BACKGROUND: Combination therapy has been proposed in treatment algorithms for idiopathic pulmonary arterial hypertension (IPAH), so the additional effects of bosentan in IPAH patients already treated with high-dose epoprostenol (EPO) was evaluated in the present study. METHODS AND RESULTS: Bosentan...See full text at original site
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引用元:
https://doi.org/10.1253/circj.72.1142
データ提供:米国国立医学図書館(NLM)
Bosentan: A Potential Oasis in the Desert of Pulmonary Arterial Hypertension
Pulmonary arterial hypertension (PAH) is a debilitating condition that affects the heart and lungs. This study investigates the additional effects of bosentan, a drug used to treat PAH, in patients already receiving high-dose epoprostenol. The researchers, like intrepid explorers traversing the vast desert of PAH, sought to understand the potential benefits of combining these two medications. This study provides valuable insights into the potential of bosentan as an adjunct therapy for PAH, offering hope for patients facing this challenging condition.
Bosentan's Effectiveness as an Adjunct Therapy for PAH
The study showed that the addition of bosentan to epoprostenol therapy led to significant improvements in hemodynamics, specifically a decrease in systolic pulmonary artery pressure. This suggests that bosentan could be a valuable tool in managing PAH, potentially offering additional benefits to patients already receiving epoprostenol treatment.
Implications for PAH Treatment and Future Research
The study's results highlight the potential of combination therapy in managing PAH, offering a potentially more effective approach to treating this complex condition. Further research should explore the optimal dosage and long-term effects of bosentan in combination with epoprostenol, ensuring its safety and efficacy in various patient populations.
Dr.Camel's Conclusion
This research offers a glimmer of hope for patients facing the challenges of pulmonary arterial hypertension. The study's findings suggest that bosentan could be a valuable addition to the treatment regimen for these patients, potentially improving their quality of life and extending their lifespan. The exploration of this new therapy exemplifies the ongoing efforts to conquer the vast desert of PAH, bringing hope to those affected by this condition.
Date :
- Date Completed 2008-09-18
- Date Revised 2019-08-19
Further Info :
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