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眶上颧突神经阻滞在小儿腺样体扁桃体切除术的应用和阿片类药物需求:一项随机临床试验。

Suprazygomatic Maxillary Nerve Blocks and Opioid Requirements in Pediatric Adenotonsillectomy: A Randomized Clinical Trial.

机构信息

Department of Anesthesiology, Perioperative, and Pain Medicine, Stanford University School of Medicine, Stanford, California.

Department of Otolaryngology-Head and Neck Surgery, Stanford University School of Medicine, Stanford, California.

出版信息

JAMA Otolaryngol Head Neck Surg. 2024 Jul 1;150(7):564-571. doi: 10.1001/jamaoto.2024.1011.

Abstract

IMPORTANCE

Pain management following pediatric adenotonsillectomies is opioid-inclusive, leading to potential complications.

OBJECTIVE

To investigate the use of suprazygomatic maxillary nerve (SZMN) blocks to reduce pain and opioid use after pediatric intracapsular adenotonsillectomy and to measure recovery duration and incidence of complications.

DESIGN, SETTING, AND PARTICIPANTS: This was a randomized, blinded, prospective single-center tertiary pediatric hospital that included 60 pediatric patients (2-14 years old) scheduled for intracapsular adenotonsillectomy from November 2021 to March 2023. Patients were excluded for having combined surgical procedures, developmental delay, coagulopathy, chronic pain history, known or predicted difficult airway, or unrepaired congenital heart disease. Participants were randomized to receive bilateral SZMN blocks (block group) or not (control group).

INTERVENTION

SZMN block administered bilaterally under general anesthesia for intracapsular adenotonsillectomy.

PRIMARY OUTCOMES AND MEASURES

Opioid consumption, FLACC (Face, Legs, Activity, Cry, Consolability) scores, and rates of opioid-free postanesthesia care unit (PACU) stay. Secondary outcomes were recovery duration and incidence of adverse effects, ie, nausea, vomiting, block site bleeding, and emergency delirium.

RESULTS

The study population included 53 pediatric patients (mean [SD] age, 6.5 [3.6] years; 29 [55%] females; 24 [45%] males); 26 were randomly assigned to the SZMN block group and 27 to the control group. The mean (SD) opioid morphine equivalent consumption during PACU stay was 0.15 (0.14) mg/kg for the 27 patients in the control group compared with 0.07 (0.11) mg/kg for the 26 patients in the block group (mean difference, 0.08; 95% CI, 0.01-0.15; Cohen d, 0.64). The block group had a higher incidence of opioid-free PACU stays (n = 7 patients; 58%) compared with the control group (n = 15 patients; 26%) (mean difference, 32%; 95% CI, 5%-53%). Patients in the block group experienced lower FLACC scores (0.7 vs 1.6; mean difference, 0.9; 95% CI, 0.2-1.6; Cohen d, 0.7). The overall occurrence of adverse events was similar in the 2 groups, with no reported nerve block-related complications.

CONCLUSIONS AND RELEVANCE

The results of the randomized clinical trial indicate that SZMN blocks are a useful adjunct tool for managing postoperative pain in pediatric intracapsular adenotonsillectomy. Use of these blocks during adenotonsillectomy provided clinically meaningful reductions of postoperative opioid consumption with a low risk of complications.

TRIAL REGISTRATION

ClinicalTrials.gov Identifier: NCT04797559.

摘要

重要性

儿科腺样体扁桃体切除术的疼痛管理包括使用阿片类药物,这可能导致潜在的并发症。

目的

研究使用 suprazygomatic 上颌神经(SZMN)阻滞来减少小儿囊内腺样体扁桃体切除术后的疼痛和阿片类药物的使用,并测量恢复时间和并发症的发生率。

设计、地点和参与者:这是一项随机、盲法、前瞻性的单中心三级儿科医院研究,纳入了 60 名小儿患者(2-14 岁),他们计划在 2021 年 11 月至 2023 年 3 月期间进行囊内腺样体扁桃体切除术。排除了合并手术、发育迟缓、凝血障碍、慢性疼痛史、已知或预测的困难气道或未修复的先天性心脏病的患者。参与者被随机分配接受双侧 SZMN 阻滞(阻滞组)或不接受(对照组)。

干预措施

在全身麻醉下双侧行 SZMN 阻滞,用于囊内腺样体扁桃体切除术。

主要结果和测量指标

阿片类药物的消耗量、FLACC(面部、腿部、活动、哭泣、安慰)评分和无阿片类药物的术后恢复室(PACU)停留率。次要结果是恢复时间和不良事件的发生率,即恶心、呕吐、阻滞部位出血和紧急谵妄。

结果

研究人群包括 53 名小儿患者(平均[标准差]年龄,6.5[3.6]岁;29[55%]名女性;24[45%]名男性);26 名被随机分配到 SZMN 阻滞组,27 名被分配到对照组。对照组 27 名患者在 PACU 停留期间平均(标准差)阿片类药物吗啡等效消耗量为 0.15(0.14)mg/kg,而阻滞组 26 名患者为 0.07(0.11)mg/kg(平均差异,0.08;95%置信区间,0.01-0.15;Cohen d,0.64)。阻滞组有更高比例的无阿片类药物 PACU 停留(n=7 名患者;58%),而对照组(n=15 名患者;26%)(平均差异,32%;95%置信区间,5%-53%)。阻滞组患者的 FLACC 评分较低(0.7 分比 1.6 分;平均差异,0.9;95%置信区间,0.2-1.6;Cohen d,0.7)。两组的总体不良事件发生率相似,无报告与神经阻滞相关的并发症。

结论和相关性

这项随机临床试验的结果表明,SZMN 阻滞是小儿囊内腺样体扁桃体切除术术后疼痛管理的有用辅助工具。在腺样体扁桃体切除术中使用这些阻滞可显著减少术后阿片类药物的消耗,且并发症风险低。

试验注册

ClinicalTrials.gov 标识符:NCT04797559。

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