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Methadone and a Clinical Pathway in Adolescent Idiopathic Scoliosis Surgery: A Historically Controlled Study

机译:美沙酮和青少年特发性脊柱侧凸手术的临床途径:历史上控制的研究

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Study Design: Historically controlled clinical trial. Objectives: Patients presenting for correction of adolescent idiopathic scoliosis (AIS) by posterior spinal fusion may benefit from structured clinical pathways. We studied the effects of implementing a published clinical pathway for the perioperative care of patients with AIS that required intraoperative use of methadone at our institution. Methods: We performed a historically controlled clinical trial of patients undergoing posterior spinal fusion for AIS by comparing a retrospectively collected control group of 25 patients with a prospective experimental group of 14 patients receiving methadone, gabapentin, propofol, and remifentanil as part of a new clinical pathway. Results: Use of the pathway decreased average pain scores evaluated by the Numeric Rating Scale in the 24 hours following surgery (4.8 [4-6] to 3.4 [2-4], P = .03 [?2.6 to ?0.2; t = ?2.3]) and postoperative opioid consumption by 76% (41 [29-51] mg to 10 [4-17] mg, P .001 [?45 to ?15; Welch’s t = 4.9]) during the same period. Improved analgesia and reduced reliance on opioids facilitated other postoperative elements of the clinical pathway and shortened the average hospital length of stay by 1 day (4 [3-6] days to 3 [3-5] days, P = .001 [?2 to ?1; U = 67, Z = ?3.3]). Conclusions: Multimodal analgesia and a clinical pathway add value in the perioperative care of patients undergoing posterior spinal fusion for AIS by improving analgesia and shortening hospitalization. The prospective arm of the trial was registered at clinicaltrials.gov under {"type":"clinical-trial","attrs":{"text":"NCT02481570","term_id":"NCT02481570"}} NCT02481570 .
机译:学习设计:历史控制的临床试验。目的:通过后脊髓融合校正青少年特发性脊柱侧凸(AIS)的患者可以从结构化的临床途径中受益。我们研究了在我们的机构术中使用AIS术后护理的发表临床途径的影响,以便在我们的机构中​​术后使用美沙酮。方法:通过比较25名患者的次临床实验组14例患者的前瞻性实验组14名患者,历史上受控临床试验,对AIS进行后脊柱融合的患者进行了近期脊柱融合。作为新临床新的临床途径。结果:在手术后24小时内(4.8 [4-6]至3.4 [2-4],P = .03 [2-4,P = .03至0.2; T = ?2.3])和术后阿片类药物消耗76%(41 [29-51] Mg至10 [4-17] Mg,P <.001 [〜45至约15; Welch的T = 4.9])。改善镇痛和降低对阿片类药物的依赖促进了临床途径的其他术后要素,并将平均医院住院时间缩短了1天(4 [3-6]至3天,P = .001 [2到?1; u = 67,z =?3.3])。结论:通过改善镇痛和缩短住院治疗AIS后脊柱融合的围手术期镇痛和临床途径增加价值。审判的前瞻性手臂在Clinicaltrials.gov下注册{“类型”:“临床试验”,“attrs”:{“text”:“nct02481570”,“term_id”:“nct02481570”}} nct02481570。

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