Department of Anatomy and Physiology, College of Veterinary Medicine, Kansas State University, Manhattan, KS.
Department of Clinical Sciences, College of Veterinary Medicine, Kansas State University, Manhattan, KS.
Am J Vet Res. 2022 Jun 13;83(8):ajvr.22.01.0014. doi: 10.2460/ajvr.22.01.0014.
To assess the pharmacokinetics, clinical efficacy, and adverse effects of injectable methadone with the pharmacokinetic enhancer fluconazole (methadone-fluconazole), compared with the standard formulation of injectable methadone, in dogs after ovariohysterectomy. We hypothesized that 2 doses of methadone-fluconazole would provide 24 hours of postoperative analgesia.
3 purpose-bred dogs (pharmacokinetic preliminary study) and 42 female dogs from local shelters (clinical trial) were included.
Pharmacokinetics were preliminarily determined. Clinical trial client-owned dogs were blocked by body weight into treatment groups: standard methadone group (methadone standard formulation, 0.5 mg/kg, SC, q 4 h; n = 20) or methadone-fluconazole group (0.5 mg/kg methadone with 2.5 mg/kg fluconazole, SC, repeated once at 6 h; n = 22). All dogs also received acepromazine, propofol, and isoflurane. Surgeries were performed by experienced surgeons, and dogs were monitored perioperatively using the Glasgow Composite Measure Pain Scale-Short Form (CMPS-SF) and sedation scales. Evaluators were masked to treatment.
Findings from pharmacokinetic preliminary studies supported that 2 doses of methadone-fluconazole provide 24 hours of drug exposure. The clinical trial had no significant differences in treatment failures or postoperative CMPS-SF scores between treatments. One dog (methadone-fluconazole group) had CMPS-SF > 6 and received rescue analgesia. All dogs had moderate sedation or less by 1 hour (methadone-fluconazole group) or 4 hours (standard methadone group) postoperatively. Sedation was completely resolved in all dogs the day after surgery.
Methadone-fluconazole with twice-daily administration was well tolerated and provided effective postoperative analgesia for dogs undergoing ovariohysterectomy. Clinical compliance and postoperative pain control may improve with an effective twice-daily formulation.
评估米索啡氟康唑(米索啡氟康唑)与注射用美沙酮标准制剂相比,在卵巢子宫切除术的狗中的药代动力学、临床疗效和不良反应。我们假设 2 剂米索啡氟康唑将提供 24 小时的术后镇痛。
包括 3 只目的繁殖犬(药代动力学初步研究)和 42 只来自当地避难所的母犬(临床试验)。
初步确定药代动力学。临床试验的客户拥有的狗根据体重分为治疗组:标准美沙酮组(美沙酮标准制剂,0.5mg/kg,SC,q4h;n=20)或米索啡氟康唑组(0.5mg/kg 米索啡氟康唑,2.5mg/kg 氟康唑,6h 重复一次;n=22)。所有狗还接受了乙酰丙嗪、异丙酚和异氟烷。手术由经验丰富的外科医生进行,狗在围手术期使用格拉斯哥复合疼痛量表-短表(CMPS-SF)和镇静量表进行监测。评估者对治疗情况进行了屏蔽。
药代动力学初步研究结果表明,2 剂米索啡氟康唑提供 24 小时的药物暴露。临床试验中,治疗失败或术后 CMPS-SF 评分在治疗之间无显著差异。1 只狗(米索啡氟康唑组)的 CMPS-SF>6,接受了镇痛抢救。所有狗在术后 1 小时(米索啡氟康唑组)或 4 小时(标准美沙酮组)时均表现出中度镇静或更少。所有狗在手术后第二天镇静完全缓解。
米索啡氟康唑每日两次给药耐受性良好,为接受卵巢子宫切除术的狗提供了有效的术后镇痛。临床依从性和术后疼痛控制可能会随着有效每日两次的制剂而改善。