Comparison Between Intraoperative Two-Space Injection Thoracic Paravertebral Block and Wound Infiltration as a Component of Multimodal Analgesia for Postoperative Pain Management After Video-Assisted Thoracoscopic Lobectomy: A Randomized Controlled Trial

Objective To compare paravertebral block under thoracoscopy with wound infiltration at an early stage after video-assisted thoracic lobectomy surgery. Design A prospective, randomized, triple-blinded, placebo-controlled trial. Setting A single-center university hospital. Participants Patients schedu...

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Veröffentlicht in:Journal of cardiothoracic and vascular anesthesia 2015-12, Vol.29 (6), p.1550-1556
Hauptverfasser: Zhang, Xuezheng, MS, Shu, Luowa, MD, Lin, Chaoxi, BS, Yang, Pei, MS, Zhou, Ying, MS, Wang, Quanguang, MS, Wu, Yiquan, MS, Xu, Xuzhong, BS, Cui, Xu, MD, Lin, Xiaoming, MD, Jin, Lielie, BS, Li, Tianzuo, MD
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Sprache:eng
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Zusammenfassung:Objective To compare paravertebral block under thoracoscopy with wound infiltration at an early stage after video-assisted thoracic lobectomy surgery. Design A prospective, randomized, triple-blinded, placebo-controlled trial. Setting A single-center university hospital. Participants Patients scheduled for video-assisted thoracic lobectomy surgery between February 20, 2014 and June 1, 2014 randomly were allocated into paravertebral block (PVB) (n = 35) and infiltration (n = 35) groups. Interventions In the PVB group, 0.5% ropivacaine was injected into the paravertebral space by the surgeon under direct vision with placebo infiltration of saline in the wounds. In the infiltration group, the wounds were infiltrated with 0.5% ropivacaine by the surgeon with a placebo paravertebral block. Subsequently, patient-controlled intravenous morphine analgesia and paracoxib were administered. Measurements and Main Results The primary endpoints were visual analog scale (VAS) pain scores at rest and on cough 0, 2, 6, and 24 hours after surgery. The secondary endpoints were the total morphine during postoperative 0 hours to 24 hours, adverse events, and patient satisfaction with the analgesia. Sixty-one patients completed the study. VAS score on cough at each time point was significantly lower (p
ISSN:1053-0770
1532-8422
DOI:10.1053/j.jvca.2015.06.013