Abstract | OBJECTIVE: METHODS: Twenty-eight PH patients (Group 1+Group 4) came from Shanghai East Hospital, Zhongshan Hospital of Fudan University and Fifth People's Hospital of Shanghai were recruited into this open-label, prospective multi-center trial between August 2012 and February 2013. They received 2.5-5.0 mg ambrisentan once daily for 12 weeks. The primary endpoint was the change in exercise capacity showed by six-minute walk distance (6MWD) from baseline to 12 weeks. Secondary endpoints included the changes in World Health Organization (WHO) function class, N-terminal brain natriuretic peptide ( NT-proBNP) and liver function test results. RESULTS: There were 9 males and 19 females with an average age of (35 ± 17) years. The value of 6MWD increased from (372 ± 86) m at baseline to (443 ± 96) m (P = 0.000) after 12 weeks. WHO functional class improved after a 12-week therapy compared to the baseline level (P = 0.000). NT-proBNP decreased from a median of 732 ng/L at baseline to 329 ng/L after 12 weeks (P = 0.046). The baseline liver function test was normal. And liver function test didn't significantly change after a 12-week therapy. CONCLUSION:
Ambrisentan therapy is well-tolerated and it improves the exercise capacity and WHO function class in Chinese PH patients.
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Authors | Fa-dong Chen, Da-xin Zhou, Ruo-min Di, Yu Zou, Wei Wei, Xue-bo Liu |
Journal | Zhonghua yi xue za zhi
(Zhonghua Yi Xue Za Zhi)
Vol. 93
Issue 34
Pg. 2736-8
(Sep 10 2013)
ISSN: 0376-2491 [Print] China |
PMID | 24360110
(Publication Type: Clinical Trial, Journal Article, Multicenter Study)
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Chemical References |
- Antihypertensive Agents
- Phenylpropionates
- Pyridazines
- ambrisentan
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Topics |
- Adolescent
- Adult
- Antihypertensive Agents
(adverse effects, therapeutic use)
- Female
- Humans
- Hypertension, Pulmonary
(drug therapy)
- Male
- Middle Aged
- Phenylpropionates
(adverse effects, therapeutic use)
- Prospective Studies
- Pyridazines
(adverse effects, therapeutic use)
- Treatment Outcome
- Young Adult
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