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Evidence-Based Complementary and Alternative Medicine
Volume 2017, Article ID 3162851, 6 pages
https://doi.org/10.1155/2017/3162851
Research Article

Clinical Effect of Electroacupuncture on Lung Injury Patients Caused by Severe Acute Pancreatitis

1Department of Anesthesiology, Tianjin Central Hospital of Gynecology Obstetrics, Tianjin 300100, China
2Department of Anesthesiology, Tianjin Nankai Hospital, Tianjin 300100, China

Correspondence should be addressed to Jianbo Yu; moc.621@11obnaijuy

Received 6 July 2016; Revised 27 October 2016; Accepted 6 March 2017; Published 29 June 2017

Academic Editor: Tse H. Huang

Copyright © 2017 Li Li et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

This study aimed to investigate the effects of electroacupuncture at the Lieque, Chize, and Zusanli points in patients with lung injury caused by severe acute pancreatitis. Patients with acute respiratory distress syndrome (ARDS) induced by severe acute pancreatitis (SAP) were randomly divided into three groups based on the treatment: conventional therapy alone (group A), electroacupuncture of nonacupoints with conventional therapy (group B), and electroacupuncture at the Lieque (LU7), Chize (LU5), and Zusanli (ST36) points (group C) once a day for 5 days. Arterial blood samples were obtained for blood gas analysis before electroacupuncture () and 3 () and 5 () days after electroacupuncture. The oxygenation index was significantly higher in all groups at and than that at , while the APACHE-II scores were decreased significantly. The expression of TNF-α was significantly decreased and the IL-10 was significantly increased in all groups at . The oxygenation index at and was significantly higher in group C than that in group B. Electroacupuncture at Lieque, Chize, and Zusanli can lessen the lung injury induced by SAP, and the mechanism may be related to the decreased TNF-α and increased IL-10 value. Clinical Registration Number is ChiCTR-ICR-15006850.