Department of Anaesthesiology, The Juliane Marie Centre, Copenhagen University Hospital, Copenhagen, Denmark.
Pain Treatment Service, Astrid Lindgren Children's Hospital, Karolinska University Hospital, Stockholm, Sweden.
Acta Anaesthesiol Scand. 2024 Nov;68(10):1359-1368. doi: 10.1111/aas.14510. Epub 2024 Aug 18.
Minor but painful medical procedures are often handled at the operating room. If safe and effective treatment options are available many procedures may be performed outside of the operating room.
OBJECTIVE(S): The objective of this study is to assess the adverse events of intranasal s-ketamine and/or sufentanil alone or as part of a multimodal analgesic regime for medical procedures outside of the operating room. Secondary outcomes included analgesic effect, doses and indications for use.
Retrospective observational study.
Tertiary care paediatric hospital.
Children 1 year up till 18 years.
INTERVENTION(S): Intranasal (IN) sufentanil (S), intranasal s-ketamine (K) or the free combination of the two drugs (SK).
MAIN OUTCOME MEASURE(S): The frequency of adverse events including serious adverse events reported by intervention.
Between 2004 and 2014, 2185 medical procedures were registered, including 652 procedures with IN SK, 1469 procedures with IN S and 64 procedures with IN K. The children's median age was 5.6 years (range 1.0-17.9). Medical procedures with at least one adverse event were 18% with IN SK, 25% with IN K and 18% with IN S. Common adverse events included episodes of vomiting (9%), nausea (8%) and dizziness (3%). In two patients receiving IN S, serious adverse events occurred. One patient had respiratory depression and bronchospasm and another patient with cerebral palsy had a seizure. Both were handled immediately and did not result in any sequelae. The median doses of intranasal sufentanil were 38% lower when combined with s-ketamine (IN SK free combination: sufentanil dose 0.5 μg/kg (range 0.2-1.3) and s-ketamine dose 0.5 mg/kg (range 0.2-1.5). IN S monotherapy, sufentanil dose 0.8 μg/kg (range 0.2-2.7)). Similar analgesic effect was reported for S and SK.
Intranasal sufentanil and/or s-ketamine are feasible for the treatment of procedural pain in an ambulatory setting with appropriate per- and post-procedural observations and trained staff.
一些轻微但疼痛的医疗程序通常在手术室进行。如果有安全有效的治疗选择,许多程序可以在手术室之外进行。
本研究旨在评估鼻内 S-氯胺酮和/或舒芬太尼单独或作为多模式镇痛方案的一部分用于手术室外医疗程序的不良事件。次要结局包括镇痛效果、剂量和适应证。
回顾性观察性研究。
三级儿科医院。
1 岁至 18 岁的儿童。
鼻内(IN)舒芬太尼(S)、鼻内 S-氯胺酮(K)或两种药物的自由组合(SK)。
干预后报告的不良事件(包括严重不良事件)的频率。
2004 年至 2014 年期间,共登记了 2185 例医疗程序,其中包括 652 例 IN SK、1469 例 IN S 和 64 例 IN K。儿童的中位年龄为 5.6 岁(范围 1.0-17.9)。至少有 1 项不良事件的医疗程序占 18%(IN SK)、25%(IN K)和 18%(IN S)。常见的不良事件包括呕吐发作(9%)、恶心(8%)和头晕(3%)。在接受 IN S 的 2 名患者中,发生了严重不良事件。一名患者出现呼吸抑制和支气管痉挛,另一名脑瘫患者发生癫痫发作。两者都得到了及时处理,没有造成任何后遗症。当与 S-氯胺酮联合使用时,鼻内舒芬太尼的中位剂量降低了 38%(IN SK 自由组合:舒芬太尼剂量 0.5 μg/kg(范围 0.2-1.3)和 S-氯胺酮剂量 0.5 mg/kg(范围 0.2-1.5)。IN S 单药治疗,舒芬太尼剂量 0.8 μg/kg(范围 0.2-2.7))。S 和 SK 报告了类似的镇痛效果。
鼻内舒芬太尼和/或 S-氯胺酮可用于在门诊环境中治疗程序性疼痛,需要进行适当的围手术期和术后观察,并配备有训练有素的工作人员。