Bettina N Nielsen, Steen W Henneberg, Eva Malmros Olsson, Stefan Lundeberg
{"title":"在门诊环境中使用舒芬太尼和/或s-氯胺酮治疗儿童手术疼痛:回顾性观察研究。","authors":"Bettina N Nielsen, Steen W Henneberg, Eva Malmros Olsson, Stefan Lundeberg","doi":"10.1111/aas.14510","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>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.</p><p><strong>Objective(s): </strong>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.</p><p><strong>Design: </strong>Retrospective observational study.</p><p><strong>Setting: </strong>Tertiary care paediatric hospital.</p><p><strong>Patients: </strong>Children 1 year up till 18 years.</p><p><strong>Intervention(s): </strong>Intranasal (IN) sufentanil (S), intranasal s-ketamine (K) or the free combination of the two drugs (SK).</p><p><strong>Main outcome measure(s): </strong>The frequency of adverse events including serious adverse events reported by intervention.</p><p><strong>Results: </strong>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.</p><p><strong>Conclusions: </strong>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.</p>","PeriodicalId":6909,"journal":{"name":"Acta Anaesthesiologica Scandinavica","volume":" ","pages":"1359-1368"},"PeriodicalIF":1.9000,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The use of intranasal sufentanil and/or s-ketamine for treatment of procedural pain in children in an ambulatory setting: A retrospective observational study.\",\"authors\":\"Bettina N Nielsen, Steen W Henneberg, Eva Malmros Olsson, Stefan Lundeberg\",\"doi\":\"10.1111/aas.14510\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>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.</p><p><strong>Objective(s): </strong>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.</p><p><strong>Design: </strong>Retrospective observational study.</p><p><strong>Setting: </strong>Tertiary care paediatric hospital.</p><p><strong>Patients: </strong>Children 1 year up till 18 years.</p><p><strong>Intervention(s): </strong>Intranasal (IN) sufentanil (S), intranasal s-ketamine (K) or the free combination of the two drugs (SK).</p><p><strong>Main outcome measure(s): </strong>The frequency of adverse events including serious adverse events reported by intervention.</p><p><strong>Results: </strong>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)). 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引用次数: 0
摘要
背景:轻微但痛苦的医疗程序通常在手术室进行。如果有安全有效的治疗方案,许多手术可以在手术室外进行:本研究的目的是评估鼻内氯胺酮和/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反应。次要结果包括镇痛效果、使用剂量和适应症:设计:回顾性观察研究:患者:1岁至18岁的儿童:干预措施:干预措施:鼻内注射舒芬太尼(IN)、鼻内注射氯胺酮(K)或两种药物的自由组合(SK):结果:2004 年至 2014 年间,2185 名医护人员使用了舒芬太尼(IN)、鼻内氯胺酮(K)或两种药物的自由组合(SK):2004年至2014年期间,共登记了2185例医疗程序,其中652例使用IN SK,1469例使用IN S,64例使用IN K。使用 IN SK、IN K 和 IN S 的医疗程序中,至少出现一次不良事件的比例分别为 18%、25% 和 18%。常见的不良反应包括呕吐(9%)、恶心(8%)和头晕(3%)。两名接受 IN S 治疗的患者出现了严重的不良反应。一名患者出现呼吸抑制和支气管痉挛,另一名脑瘫患者出现癫痫发作。这两起事件都得到了及时处理,没有造成任何后遗症。与 s-Ketamine 联用时,鼻内舒芬太尼的中位剂量降低了 38%(IN SK 自由联用:舒芬太尼剂量为 0.5 μg/kg(范围为 0.2-1.3),s-Ketamine 剂量为 0.5 mg/kg(范围为 0.2-1.5)。在 S 单一疗法中,舒芬太尼剂量为 0.8 μg/kg(范围为 0.2-2.7))。S 和 SK 的镇痛效果相似:结论:在非卧床环境中,通过适当的术前术后观察和训练有素的工作人员,鼻内舒芬太尼和/或氯胺酮可用于治疗手术疼痛。
The use of intranasal sufentanil and/or s-ketamine for treatment of procedural pain in children in an ambulatory setting: A retrospective observational study.
Background: 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.
Design: Retrospective observational study.
Setting: Tertiary care paediatric hospital.
Patients: 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.
Results: 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.
Conclusions: 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.
期刊介绍:
Acta Anaesthesiologica Scandinavica publishes papers on original work in the fields of anaesthesiology, intensive care, pain, emergency medicine, and subjects related to their basic sciences, on condition that they are contributed exclusively to this Journal. Case reports and short communications may be considered for publication if of particular interest; also letters to the Editor, especially if related to already published material. The editorial board is free to discuss the publication of reviews on current topics, the choice of which, however, is the prerogative of the board. Every effort will be made by the Editors and selected experts to expedite a critical review of manuscripts in order to ensure rapid publication of papers of a high scientific standard.