Evaluation of ultrasound-guided suprazygomatic maxillary nerve block in functional endoscopic sinus surgery for postoperative pain relief: A randomised controlled trial

被引:0
|
作者
Neupane, Adhip [1 ]
Jain, Divya [1 ]
Arora, Suman [1 ]
Gandhi, Komal [1 ]
Singla, Varun [1 ]
Goel, Nitika [1 ]
Virk, Ramandeep Singh [2 ]
Mohindra, Satyawati [2 ]
机构
[1] Postgrad Inst Med Educ & Res, Dept Anesthesia & Intens Care, Sect 12, Chandigarh 160012, India
[2] Postgrad Inst Med Educ & Res, Dept Otorhinolaryngol, Chandigarh, India
关键词
Functional endoscopic sinus surgery; nerve blocks; numerical rating scale; postoperative pain; regional nerve block; suprazygomatic maxillary nerve block; ultrasound; BUPIVACAINE;
D O I
10.4103/ija.ija_81_24
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Background and Aims:Postoperative pain can impede functional recovery and delay hospital discharge after functional endoscopic sinus surgery (FESS). The study aimed to assess the efficacy of ultrasound (USG)-guided suprazygomatic maxillary nerve block (SZMNB) for postoperative pain in FESS. Methods:Forty-eight adult patients between 18 and 65 years of age with American Society of Anesthesiologists physical status I and II and scheduled to undergo FESS were enroled in this randomised controlled study. Patients were randomly allocated to either receive USG-guided SZMNB with general anaesthesia (n = 24) or general anaesthesia alone (n = 24). The numerical rating scale (NRS) pain score in the immediate postoperative period was recorded as the primary outcome. A total of 24 h postoperative rescue analgesic consumption, surgeon satisfaction score, postoperative haemodynamics, and postoperative complications were noted as secondary outcomes. Results:The median (interquartile range) of the NRS pain score in the immediate postoperative period was 0 (0-0.25)[95% confidence interval (CI): 0, 0.08] in the block group compared to 2 (1.75-3) [95% CI: 1.60, 2.40] in the control group, P < 0.001]. Pain scores were significantly reduced at all time intervals till 24 h after surgery (P < 0.001). None of the patients required rescue analgesia in the block group. In contrast, eight patients required diclofenac 75 mg intravenous as rescue analgesia within 1 h of surgery and ten patients within 1-6 h of surgery in the control group. Other secondary outcomes were comparable between groups (P > 0.05). Conclusion:The USG-guided SZMNB provides excellent postoperative analgesia for patients undergoing FESS without significant side effects.
引用
收藏
页码:706 / 711
页数:6
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