1. Analgesic efficacy of postoperative bilateral, ultrasound-guided, posterior transversus abdominis plane block for laparoscopic colorectal cancer surgery: a randomized, prospective, controlled study
- Author
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Tao Zhu, Qi-Lin Liu, Yi-Rong Chen, Yi Han, Yang Zhao, Han-Ying Zhang, and Zong-Yi Yuan
- Subjects
Laparoscopic surgery ,Male ,medicine.medical_treatment ,Analgesic ,Placebo ,lcsh:RD78.3-87.3 ,03 medical and health sciences ,0302 clinical medicine ,Double-Blind Method ,030202 anesthesiology ,Transversus Abdominis Plane Block ,Interquartile range ,Analgesia technique ,medicine ,Humans ,Ropivacaine ,030212 general & internal medicine ,Prospective Studies ,Anesthetics, Local ,Adverse effect ,Tramadol ,Ultrasonography, Interventional ,Postoperative Care ,Pain, Postoperative ,business.industry ,Nerve Block ,Middle Aged ,Drug Utilization ,Analgesics, Opioid ,Anesthesiology and Pain Medicine ,lcsh:Anesthesiology ,Anesthesia ,Colorectal cancer surgery ,Female ,Laparoscopy ,business ,Colorectal Neoplasms ,TAP block ,medicine.drug ,Research Article - Abstract
Background We assessed whether a postoperative bilateral, ultrasound-guided, posterior transversus abdominis plane (TAP) block could reduce 24 h rescue tramadol requirement compared with placebo in patients undergoing elective laparoscopic colorectal cancer surgery. Methods Patients scheduled to undergo elective laparoscopic surgery following the diagnosis of colorectal cancer were included in this study and randomized into Group and Group Control. The patients received a postoperative bilateral, ultrasound-guided, posterior TAP block in either 20 mL of 0.5% ropivacaine (Group TAP) per side or an equivalent volume of normal saline (Group Control). The primary outcome was the cumulative consumption of rescue tramadol within 24 h after the surgery. Secondary endpoints included (1) resting and movement numerical rating scale (NRS) pain scores at 2, 4, 6, 12, 24, 48, and 72 h; (2) incidences of related side effects; (3) time to the first request for rescue tramadol; (4) patient satisfaction regarding postoperative analgesia; (5) time to restoration of intestinal function; (6) time to mobilization; and (7) the length of hospital stay. Results In total, 92 patients were randomized, and 82 patients completed the analysis. The total rescue tramadol requirement (median [interquartile range]) within the first 24 h was lower in Group TAP (0 [0, 87.5] mg) than in Group Control (100 [100, 200] mg), P P P = 0.002), which was similar on days 2 (P = 0.702) and 3 (P = 0.551), compared with the Group Control. A few incidences of opioid-related side effects (P Conclusions A postoperative bilateral, ultrasound-guided, posterior TAP block resulted in better pain management and a faster recovery in patients undergoing laparoscopic colorectal cancer surgery, without adverse effects. Trial registration The study was registered at http://www.chictr.org.cn (ChiCTR-IPR-17012650; Sep 12, 2017).
- Published
- 2021