Combination therapy of prostacyclin for pulmonary hypertension in congenital heart disease
Background: Pulmonary arterial hypertension (PAH) is a recognized complication of congenital heart disease. Despite differences in etiology and pathophysiology, successful therapy for idiopathic PAH may benefit in patients with congenital heart disease. We theorized that combination of oral and aero...
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th-mahidol.168922018-06-21T15:24:57Z Combination therapy of prostacyclin for pulmonary hypertension in congenital heart disease Kritvikrom Durongpisitkul Decho Jakrapanichakul Duangmanee Laohaprasitiporn Jarupim Soongswang Prakul Chanthong Apichart Nana Mahidol University Medicine Background: Pulmonary arterial hypertension (PAH) is a recognized complication of congenital heart disease. Despite differences in etiology and pathophysiology, successful therapy for idiopathic PAH may benefit in patients with congenital heart disease. We theorized that combination of oral and aerosolization prostacyclin will benefit this group of patients in long term. Material and Method: The study design was single group and open label study with intention to treat for patients with congenital heart disease with pulmonary artery (PA pressure) more than 50% of systemic pressure. All patients were given a combination of orally given beraprost sodium and inhalation of iloprostfor 12 months. Data were collected prospectively consisting of functional class, O2 saturation, 6-minute walk test and right ventricular systolic pressure (RVSP). Results: There were 23 patients with an average right ventricular systolic pressure (± SD) of 94.8 ± 14.5 mmHg and with average age of 27.8 ± 14.9 years (2.5 to 50 years). The average oxygen saturation was 87.9 ± 7 %. There were 12 patients with post surgical repair or cardiac catheterization interventional procedure and 11 with and Eisenmenger's syndrome. There were significant improvement of 6-minute-walk test from an average of 268 ± 70 meters to 308 ± 57 meters at the end of 12 months. The functional class of patients was also improving. However, there were no significant different in oxygen saturation. Conclusion: Combination therapy of oral and inhalation of aerosolized vasodilators is a fascinating concept in the therapy of pulmonary hypertension. Treated patients showed an improvement in exercise capacity and right ventricular systolic pressure without a worsening in oxygen saturation. 2018-06-21T08:24:57Z 2018-06-21T08:24:57Z 2005-08-01 Article Journal of the Medical Association of Thailand. Vol.88, No.SUPPL. 8 (2005) 01252208 01252208 2-s2.0-31744446401 https://repository.li.mahidol.ac.th/handle/123456789/16892 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=31744446401&origin=inward |
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Medicine Kritvikrom Durongpisitkul Decho Jakrapanichakul Duangmanee Laohaprasitiporn Jarupim Soongswang Prakul Chanthong Apichart Nana Combination therapy of prostacyclin for pulmonary hypertension in congenital heart disease |
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Background: Pulmonary arterial hypertension (PAH) is a recognized complication of congenital heart disease. Despite differences in etiology and pathophysiology, successful therapy for idiopathic PAH may benefit in patients with congenital heart disease. We theorized that combination of oral and aerosolization prostacyclin will benefit this group of patients in long term. Material and Method: The study design was single group and open label study with intention to treat for patients with congenital heart disease with pulmonary artery (PA pressure) more than 50% of systemic pressure. All patients were given a combination of orally given beraprost sodium and inhalation of iloprostfor 12 months. Data were collected prospectively consisting of functional class, O2 saturation, 6-minute walk test and right ventricular systolic pressure (RVSP). Results: There were 23 patients with an average right ventricular systolic pressure (± SD) of 94.8 ± 14.5 mmHg and with average age of 27.8 ± 14.9 years (2.5 to 50 years). The average oxygen saturation was 87.9 ± 7 %. There were 12 patients with post surgical repair or cardiac catheterization interventional procedure and 11 with and Eisenmenger's syndrome. There were significant improvement of 6-minute-walk test from an average of 268 ± 70 meters to 308 ± 57 meters at the end of 12 months. The functional class of patients was also improving. However, there were no significant different in oxygen saturation. Conclusion: Combination therapy of oral and inhalation of aerosolized vasodilators is a fascinating concept in the therapy of pulmonary hypertension. Treated patients showed an improvement in exercise capacity and right ventricular systolic pressure without a worsening in oxygen saturation. |
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Mahidol University |
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Mahidol University Kritvikrom Durongpisitkul Decho Jakrapanichakul Duangmanee Laohaprasitiporn Jarupim Soongswang Prakul Chanthong Apichart Nana |
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Article |
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Kritvikrom Durongpisitkul Decho Jakrapanichakul Duangmanee Laohaprasitiporn Jarupim Soongswang Prakul Chanthong Apichart Nana |
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Kritvikrom Durongpisitkul |
title |
Combination therapy of prostacyclin for pulmonary hypertension in congenital heart disease |
title_short |
Combination therapy of prostacyclin for pulmonary hypertension in congenital heart disease |
title_full |
Combination therapy of prostacyclin for pulmonary hypertension in congenital heart disease |
title_fullStr |
Combination therapy of prostacyclin for pulmonary hypertension in congenital heart disease |
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Combination therapy of prostacyclin for pulmonary hypertension in congenital heart disease |
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combination therapy of prostacyclin for pulmonary hypertension in congenital heart disease |
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2018 |
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https://repository.li.mahidol.ac.th/handle/123456789/16892 |
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