短暂的无意识镇静治疗痛苦的儿科肿瘤手术。在适当的监测下静脉注射甲氧己酮是安全有效的。

A E Schwanda, D R Freyer, D J Sanfilippo, R A Axtell, J B Fahner, R M Hackbarth, N E Hassan, J S Kopec, M J Waskerwitz
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引用次数: 0

摘要

目的:我们在此报告我们使用静脉注射甲氧六酮(MHX)的经验,这是一种超短效巴比妥酸盐,用于儿科肿瘤门诊患者进行痛苦的侵入性手术的短暂无意识镇静。方法:根据已公布的儿童深度镇静监测指南,在手术前立即给予1.0 mg/kg MHX,局部给予1%的xylocaine,并在手术过程中另外滴定MHX以保持对疼痛的最小反应。本文所报道的临床资料是回顾性地从永久医疗记录中收集的。结果:本文报告的数据包括33例患者的132例可评估的连续手术,年龄从1.6岁到20.5岁不等。患者平均接受4 +/- 3次手术,每次手术的平均总MHX剂量为5.8 +/- 2.1 mg/kg。从镇静开始到完全唤醒的平均时间长度为30±12分钟。23例(17.4%)手术与舒张压或心率低于年龄静息正常范围的临床不显著下降相关。6例患者中的8例(6.1%)手术伴有无需干预的轻微并发症,如短暂行为改变、短暂性肌阵挛和轻微喘鸣。5例患者中5例手术(3.8%)需要简单吸痰来控制分泌物。2例患者中仅有2例手术(1.5%)需要短暂的袋罩通气加吸痰治疗疑似喉痉挛。没有人需要插管。与没有并发症的患者相比,有并发症的患者的临床特征或MHX剂量没有差异。所有手术均以令人满意的镇静水平完成。结论:我们的经验表明,在适当的监测下,MHX是一种安全有效的药物,可用于儿科肿瘤门诊镇静项目。
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Brief unconscious sedation for painful pediatric oncology procedures. Intravenous methohexital with appropriate monitoring is safe and effective.

Purpose: We report here our experience in using intravenous methohexital (MHX), an ultrashort-acting barbiturate, for brief unconscious sedation of pediatric oncology outpatients undergoing painful, invasive procedures.

Methods: Following published monitoring guidelines for deep pediatric sedation, 1.0 mg/kg MHX was administered immediately before the procedure, 1% xylocaine was given locally, and MHX was additionally titrated to maintain minimal response to pain during the procedure. Clinical data reported here were gathered retrospectively from permanent medical records.

Results: Data reported here represent 132 evaluable consecutive procedures in 33 patients ranging in age from 1.6 to 20.5 years. Patients underwent an average of 4 +/- 3 procedures and received a mean total MHX dose per procedure of 5.8 +/- 2.1 mg/kg. The mean length of time from start of sedation to full arousability was 30 +/- 12 min. Twenty-three (17.4%) procedures were associated with clinically insignificant decreases in diastolic blood pressure or heart rate below resting normal ranges for age. Eight (6.1%) procedures in six patients were associated with minor complications requiring no intervention, such as transient behavioral changes, transient myoclonus, and minimal stridor. Five procedures (3.8%) in five patients required simple suctioning to manage secretions. Only two procedures (1.5%) in two patients required brief bag-mask ventilation plus suctioning for suspected laryngospasm. None required intubation. No differences in clinical features or MHX doses were noted for patients with, as compared to those without, complications. All procedures were completed with a satisfactory level of sedation.

Conclusions: Our experience indicates that MHX, with appropriate monitoring as described here, is a safe and effective agent for use in pediatric oncology outpatient sedation programs.

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