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. 2021 Oct 15;13(10):11522-11530.
eCollection 2021.

Bosentan combined with sildenafil in the treatment of COPD patients with pulmonary arterial hypertension

Affiliations

Bosentan combined with sildenafil in the treatment of COPD patients with pulmonary arterial hypertension

Ying Li et al. Am J Transl Res. .

Abstract

Objective: To explore the impacts of bosentan combined with sildenafil on chronic obstructive pulmonary disease (COPD) patients with pulmonary arterial hypertension (PAH).

Methods: From April 2019 to October 2020, 90 COPD patients with PAH diagnosed in our hospital were recruited and divided into groups A and B. The patients in group A (50 cases) were treated with bosentan combined with sildenafil, and the patients in group B (40 cases) were administered bosentan combined with iloprost solution for inhalation. The PAH conditions, the heart rates (HR), the cardiac function, the pulmonary function, the blood gas indexes, the inflammatory factor expressions, the incidences of adverse reactions, the overall response rates (ORR), and the patient satisfaction levels were determined or evaluated.

Results: Compared with group B, the patients in group A had better recovered PAH, HR, cardiac function, pulmonary function, and blood gas indexes, lower inflammatory factor expression levels and a lower incidence of adverse reactions, as well as higher ORR and higher satisfaction levels.

Conclusion: Bosentan combined with sildenafil can reduce pulmonary artery pressure and promote the recovery of cardiopulmonary function in COPD patients with PAH.

Keywords: Chronic obstructive pulmonary disease; bosentan; pulmonary arterial hypertension; sildenafil.

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Conflict of interest statement

None.

Figures

Figure 1
Figure 1
The pulmonary artery pressures and the heart rates in the two groups of patients. A. Pulmonary artery pressure: both groups of patients have significantly changed pulmonary artery pressure, and it was lower in group A than in group B after the treatment (P<0.05). B. Heart rate: both groups of patients have significantly changed heart rates, and they were lower in group A than in group B after the treatment (P<0.05). Notes: *P<0.05 vs. on admission, #P<0.05 vs. group B.
Figure 2
Figure 2
Cardiac function of two groups of patients. A. 6MWD: both groups of patients have significantly changed 6MWD, which was higher in group A than in group B after the treatment (P<0.05). B. RVEF: both groups of patients have significantly changed RVEF, which was higher in group A than in group B after the treatment (P<0.05). Notes: *P<0.05 vs. on admission, #P<0.05 vs. group B.
Figure 3
Figure 3
The pulmonary function and blood gas indexes of two groups of patients. A. FEV1: both groups of patients have significantly changed FEV1, which was higher in group A than in group B after the treatment (P<0.05). B. FVC: both groups of patients have significantly changed FVC, which was higher in group A than in group B after the treatment (P<0.05). C. FEV1/FVC: both groups of patients have significantly changed FEV1/FVC, which was higher in group A than in group B after the treatment (P<0.05). D. PaO2: there were significant changes in both groups in PaO2, and PaO2 in group A was higher than that in group B after treatment (P<0.05). E. PaCO2: there were significant changes in both groups in PaCO2, and PaCO2 in group A was lower than that in group B after treatment (P<0.05). Notes: *P<0.05 vs. on admission, #P<0.05 vs. group B.
Figure 4
Figure 4
The inflammatory factor levels of the two groups of patients. A. IL-13: both groups of patients have significantly changed IL-13, which was lower in group A than in group B after treatment (P<0.05). B. IL-17: both groups of patients have significantly changed IL-17, which was lower in group A than in group B after treatment (P<0.05). C. CRP: both groups of patients have significantly changed CRP, which is lower in group A than in group B after treatment (P<0.05). Notes: *P<0.05 vs. on admission, #P<0.05 vs. group B.

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