首页> 外文期刊>Journal of addiction medicine >Rapid Micro-induction of Buprenorphine/Naloxone for Opioid Use Disorder in a Critically ill Intubated Patient: A Case Report
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Rapid Micro-induction of Buprenorphine/Naloxone for Opioid Use Disorder in a Critically ill Intubated Patient: A Case Report

机译:用于阿片类药物的丁丙诺啡/纳洛酮的快速微观诱导在批判性插管患者中使用障碍:案例报告

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Background: Buprenorphine/naloxone has been shown to be an effective treatment of opioid use disorder. According to the Canadian National clinical practice guideline on the management of opioid use disorders, given the superior safety profile of buprenorphine/naloxone and its potential for flexible take-home dosing in comparison to other opioid agonist medication it is strongly recommended to initiate opioid agonist treatment with buprenorphine/naloxone as the preferred first-line treatment when possible. Due to its pharmacological properties induction can be challenging, requiring the cessation of all opioids for a certain amount of time to avoid the risk of precipitated withdrawal symptoms. For this reason, buprenorphine/naloxone is not initiated for the treatment of opioid use disorder in critically ill patients where continuous infusion of opioids are required for maintenance of sedation resulting in a missed opportunity for first line treatment of that patient's opioid use disorder. Case Summary: We present a case of a 29-year-old female with opioid use disorder admitted for infective endocarditis and septic shock requiring intubation for hypoxic respiratory failure secondary to bilateral lung septic emboli with a high opioid debt requiring higher than typical doses of fentanyl and dexmedetomidine infusions to maintain sedation with clinical objective sign of inadequate treatment of her pain and opioid withdrawal. She was successfully started on buprenorphine/naloxone using a rapid micro-induction technique that did not cause precipitated withdrawal or require cessation of her fentanyl infusion. Conclusion: This case illustrates a new method for starting buprenorphine/naloxone in a critically ill intubated patient, where buprenorphine/naloxone was never a consideration in this specific patient population. Scientific Significance: This method can be used to minimize barriers to opioid agonist therapy in intubated patients
机译:背景:丁丙诺啡/纳洛酮已被证明是阿片类药物使用障碍的有效治疗方法。根据《加拿大阿片类药物使用障碍管理国家临床实践指南》,鉴于丁丙诺啡/纳洛酮具有优越的安全性,且与其他阿片类激动剂药物相比,它具有灵活的带回家给药的潜力,因此强烈建议在可能的情况下,开始使用丁丙诺啡/纳洛酮作为首选一线治疗的阿片类激动剂治疗。由于其药理学特性,诱导可能具有挑战性,需要在一定时间内停止所有阿片类药物,以避免突然出现戒断症状的风险。因此,丁丙诺啡/纳洛酮不能用于治疗危重患者的阿片类药物使用障碍,因为需要持续输注阿片类药物以维持镇静,从而错过了对该患者阿片类药物使用障碍进行一线治疗的机会。病例总结:我们报告一例29岁女性,患有阿片类药物使用障碍,因感染性心内膜炎和败血性休克入院,因双侧肺败血性栓子继发的缺氧性呼吸衰竭需要插管,阿片类药物负债高,需要输注高于典型剂量的芬太尼和右美托咪定来维持镇静,临床客观症状为不充分治疗她的疼痛和阿片类药物戒断。她成功地开始使用丁丙诺啡/纳洛酮,使用快速微量诱导技术,不会导致突然停药或停止芬太尼输注。结论:本病例说明了一种在危重病人插管时开始使用丁丙诺啡/纳洛酮的新方法,而丁丙诺啡/纳洛酮在这一特定患者群体中从未考虑过。科学意义:该方法可用于最小化插管患者阿片受体激动剂治疗的障碍

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