Opioid-free versus opioid-based anesthesia in major spine surgery: a prospective, randomized, controlled clinical trial.

IF 2.9 3区 医学 Q1 ANESTHESIOLOGY Minerva anestesiologica Pub Date : 2024-06-01 DOI:10.23736/S0375-9393.24.17962-X
Hanane Barakat, Rony Al Nawwar, Jessy Abou Nader, Marie Aouad, Vanda Yazbeck Karam, Linda Gholmieh
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Abstract

Background: Major spine surgery is associated with severe postoperative pain and increased opioid consumption. Opioid-free anesthesia (OFA) is thought to provide adequate intraoperative analgesia with reduced postoperative opioid consumption. The aim of this study is to compare the impact of intraoperative OFA approach to the conventional opioid-based anesthesia (OBA) on postoperative pain, opioid consumption, and related side effects in patients undergoing multilevel spinal fusion surgery.

Methods: Forty-eight patients undergoing elective major spine surgery were randomly allocated to either receive intraoperative dexmedetomidine and lidocaine (OFA group) or fentanyl during induction and intraoperative remifentanil (OBA group). All patients received intraoperative sevoflurane, propofol, rocuronium, ketamine, dexamethasone, ondansetron and postoperative paracetamol and patient-controlled analgesia device set to deliver intravenous morphine for 48 hours after surgery. Postoperative pain was measured using numerical rating scale. Opioid side effects were documented, when present.

Results: OFA group required less morphine in the first 24 hours post-surgery (17.28±12.25 mg versus 27.96±19.75 mg, P<0.05). The incidence of postoperative nausea and vomiting (PONV) was significantly lower in the OFA group. More patients in the OFA group required antihypertensive medications compared to patients in the OBA group (P<0.05). In the post anesthesia care unit, OFA patients had a significantly longer stay than OBA patients (114.1±49.33 min versus 89.96±30.71 min, P<0.05).

Conclusions: OFA can be an alternative to OBA in patients undergoing multilevel spine fusion surgery. OFA reduces opioids consumption in the first 24 hours and PONV.

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脊柱大手术中的无阿片麻醉与阿片麻醉:一项前瞻性随机对照临床试验。
背景:脊柱大手术与严重的术后疼痛和阿片类药物消耗量增加有关。无阿片麻醉(OFA)被认为能提供充分的术中镇痛,减少术后阿片类药物的消耗。本研究的目的是比较术中无阿片麻醉方法与传统的阿片类药物麻醉(OBA)对多层次脊柱融合手术患者术后疼痛、阿片类药物消耗及相关副作用的影响:48名接受择期脊柱大手术的患者被随机分配到术中使用右美托咪定和利多卡因(OFA组)或诱导期间使用芬太尼和术中使用瑞芬太尼(OBA组)。所有患者在术中均接受七氟醚、丙泊酚、罗库洛铵、氯胺酮、地塞米松、昂丹司琼和术后扑热息痛,术后 48 小时内使用患者自控镇痛装置静脉注射吗啡。术后疼痛采用数字评分法进行测量。如果出现阿片类药物副作用,则记录在案:结果:OFA 组在术后头 24 小时内对吗啡的需求量较少(17.28±12.25 毫克对 27.96±19.75 毫克,PC 结论:OFA 可替代手术镇痛:对于接受多椎间融合手术的患者,OFA可替代OBA。OFA 可减少术后 24 小时内阿片类药物的用量和 PONV。
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来源期刊
Minerva anestesiologica
Minerva anestesiologica 医学-麻醉学
CiteScore
4.50
自引率
21.90%
发文量
367
审稿时长
4-8 weeks
期刊介绍: Minerva Anestesiologica is the journal of the Italian National Society of Anaesthesia, Analgesia, Resuscitation, and Intensive Care. Minerva Anestesiologica publishes scientific papers on Anesthesiology, Intensive care, Analgesia, Perioperative Medicine and related fields. Manuscripts are expected to comply with the instructions to authors which conform to the Uniform Requirements for Manuscripts Submitted to Biomedical Editors by the International Committee of Medical Journal Editors.
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