Clinical characteristics of pulmonary hypertension in bronchiectasis

Lan Wang, Sen Jiang, Jingyun Shi, Sugang Gong, Qinhua Zhao, Rong Jiang, Ping Yuan, Bigyan Pudasaini, Jing He, Zhicheng Jing, Jinming Liu

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Front. Med. ›› 2016, Vol. 10 ›› Issue (3) : 336-344. DOI: 10.1007/s11684-016-0461-z
RESEARCH ARTICLE
RESEARCH ARTICLE

Clinical characteristics of pulmonary hypertension in bronchiectasis

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Abstract

Pulmonary hypertension (PH), as a complication of bronchiectasis, is associated with increased mortality. However, hemodynamic characteristics and the efficacy of pulmonary arterial hypertension (PAH) therapies in patients with bronchiectasis and PH remain unknown. Patients with bilateral bronchiectasis and concurrent PH were included in the study. Patient characteristics at baseline and during follow-up, as well as survival, were analyzed. This observational study was conducted in 36 patients with a mean age of 51.5 years (range, 17‒74 years). The 6 min walking distance was 300.8±93.3 m. The mean pulmonary arterial pressure (PAP) was 41.5±11.7 mmHg, cardiac output was 5.2±1.4 L/min, and pulmonary vascular resistance was 561.5±281.5 dyn·s·cm5. The mean PAP was>35 mmHg in 75% of the cases. Mean PAP was inversely correlated with arterial oxygen saturation values (r = −0.45, P = 0.02). In 24 patients who received oral PAH therapy, systolic PAP was reduced from 82.4±27.0 mmHg to 65.5±20.9 mmHg (P = 0.025) on echocardiography after a median of 6 months of follow-up. The overall probability of survival was 97.1% at 1 year, 83.4% at 3 years, and 64.5% at 5 years. Given the results, we conclude that PH with severe hemodynamic impairment can occur in patients with bilateral bronchiectasis, and PAH therapy might improve hemodynamics in such patients. Prospective clinical trials focusing on this patient population are warranted.

Keywords

bronchiectasis / hemodynamics / pulmonary hypertension

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Lan Wang, Sen Jiang, Jingyun Shi, Sugang Gong, Qinhua Zhao, Rong Jiang, Ping Yuan, Bigyan Pudasaini, Jing He, Zhicheng Jing, Jinming Liu. Clinical characteristics of pulmonary hypertension in bronchiectasis. Front. Med., 2016, 10(3): 336‒344 https://doi.org/10.1007/s11684-016-0461-z

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Acknowledgements

The authors thank Drs Wenlan Yang, Jian Guo, and the staffs of the department of Pulmonary Function Testing of Shanghai Pulmonary Hospital, Tongji University for their support.

Compliance with ethics guidelines

Lan Wang, Sen Jiang, Jingyun Shi, Sugang Gong, Qinhua Zhao, Rong Jiang, Ping Yuan, Bigyan Pudasaini, Jing He, and Jinming Liu declare that they have no conflict of interest. All procedures followed were in accordance with the ethical standards of the responsible committee on human experimentation (institutional and national) and with the Helsinki Declaration of 1975, as revised in 2000(5). Informed consent was obtained from all patients for being included in the study.

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