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Study on the clinical efficacy of specific phosphodiesterase inhibitor in patients with pulmonary hypertension due to left heart disease

  • Authors:
    • Bing Han
    • Qingli Wang
  • View Affiliations / Copyright

    Affiliations: The Key Laboratory of Cardiovascular Remodeling and Function Research, Chinese Ministry of Education and Chinese Ministry of Health, The State and Shandong Joint Key Laboratory of Translational Cardiovascular Medicine, Qilu Hospital of Shandong University, Jinan, Shandong 250012, P.R. China, Internal Medicine Cardiovascular Department, The Sixth People's Hospital of Jinan, Jinan, Shandong 250200, P.R. China
    Copyright: © Han et al. This is an open access article distributed under the terms of Creative Commons Attribution License [CC BY_NC 4.0].
  • Pages: 1175-1186
    |
    Published online on: June 13, 2018
       https://doi.org/10.3892/etm.2018.6310
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Abstract

Pulmonary hypertension due to left heart disease (PH‑LHD) is caused by left ventricular (LV) systolic and/or diastolic dysfunction and left heart valve disease. LV diseases lead to left ventricular filling pressure increases, pulmonary venous obstruction and pulmonary venous pressure increases, and thus to secondary PH. Exercise tolerance is lower and fatality rates are higher in patients with PH‑LHD than those in subjects with normal pulmonary arterial pressure. In spite of the progress in the study of the mechanisms of PH‑LHD in recent years, no specific treatment is currently available. The efficacy and safety of targeted therapies for pulmonary arterial hypertension remain to be fully established. In the present study, PH‑LHD patients were treated with milrinone injection. It was concluded that milrinone significantly reduces pulmonary artery systolic pressure (PASP) in patients with PH‑LHD, and significantly improves the cardiac structure, cardiac function and biochemical indexes. PASP was significantly correlated with the left atrial diameter, LV end diastolic diameter, LV ejection fraction, tricuspid annular plane systolic excursion, right ventricular fractional area change, N‑terminal pro‑B‑type natriuretic peptide and hypersensitive C‑reactive protein.
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Copy and paste a formatted citation
Spandidos Publications style
Han B and Wang Q: Study on the clinical efficacy of specific phosphodiesterase inhibitor in patients with pulmonary hypertension due to left heart disease. Exp Ther Med 16: 1175-1186, 2018.
APA
Han, B., & Wang, Q. (2018). Study on the clinical efficacy of specific phosphodiesterase inhibitor in patients with pulmonary hypertension due to left heart disease. Experimental and Therapeutic Medicine, 16, 1175-1186. https://doi.org/10.3892/etm.2018.6310
MLA
Han, B., Wang, Q."Study on the clinical efficacy of specific phosphodiesterase inhibitor in patients with pulmonary hypertension due to left heart disease". Experimental and Therapeutic Medicine 16.2 (2018): 1175-1186.
Chicago
Han, B., Wang, Q."Study on the clinical efficacy of specific phosphodiesterase inhibitor in patients with pulmonary hypertension due to left heart disease". Experimental and Therapeutic Medicine 16, no. 2 (2018): 1175-1186. https://doi.org/10.3892/etm.2018.6310
Copy and paste a formatted citation
x
Spandidos Publications style
Han B and Wang Q: Study on the clinical efficacy of specific phosphodiesterase inhibitor in patients with pulmonary hypertension due to left heart disease. Exp Ther Med 16: 1175-1186, 2018.
APA
Han, B., & Wang, Q. (2018). Study on the clinical efficacy of specific phosphodiesterase inhibitor in patients with pulmonary hypertension due to left heart disease. Experimental and Therapeutic Medicine, 16, 1175-1186. https://doi.org/10.3892/etm.2018.6310
MLA
Han, B., Wang, Q."Study on the clinical efficacy of specific phosphodiesterase inhibitor in patients with pulmonary hypertension due to left heart disease". Experimental and Therapeutic Medicine 16.2 (2018): 1175-1186.
Chicago
Han, B., Wang, Q."Study on the clinical efficacy of specific phosphodiesterase inhibitor in patients with pulmonary hypertension due to left heart disease". Experimental and Therapeutic Medicine 16, no. 2 (2018): 1175-1186. https://doi.org/10.3892/etm.2018.6310
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