Sacha Gretchen L, Foreman Maria G, Kyllonen Kay, Rodriguez Ricardo J
J Pediatr Pharmacol Ther. 2017 May-Jun;22(3):207-211. doi: 10.5863/1551-6776-22.3.207.
Limited data support how to safely and effectively treat refractory pain and agitation in neonates and infants. Gabapentin has been used in this patient population and has shown promising results, yet there is still a paucity of data about its clinical efficacy. There is a need for a larger evaluation to determine its effectiveness. This study describes one institution's experience with gabapentin for the treatment of refractory pain and agitation in the neonatal intensive care unit (NICU).
This was a retrospective, observational evaluation of patients who received gabapentin in the level IV NICU at the Cleveland Clinic Children's Hospital. Changes in neonatal pain, agitation, and sedation scale (N-PASS) scores and analgesic and sedative medication requirements were analyzed, as were gabapentin dose requirements and adverse reactions.
Between January 2012 and November 2015, 22 patients received gabapentin and were included in this study. The average gabapentin starting dose was 10.2 mg/kg/day, with maximum doses up to 25.5 mg/kg/day. The median N-PASS score at gabapentin therapy initiation was 3.1 and after gabapentin initiation the last N-PASS score documented was 0 in all but 5 patients. Gabapentin use reduced the need for analgesic or sedative medications. The drug was well tolerated, and only 1 patient experienced an adverse reaction to gabapentin (i.e., nystagmus).
Gabapentin was well tolerated and associated with decreases in pain scores. It's use resulted in decreased requirements for analgesic and sedative medications. Gabapentin therapy appears to be an effective option for neonates and infants with refractory pain and agitation.
关于如何安全有效地治疗新生儿和婴儿难治性疼痛及躁动的数据有限。加巴喷丁已用于该患者群体并显示出有前景的结果,但关于其临床疗效的数据仍然匮乏。需要进行更大规模的评估以确定其有效性。本研究描述了一家机构使用加巴喷丁治疗新生儿重症监护病房(NICU)难治性疼痛及躁动的经验。
这是一项对在克利夫兰诊所儿童医院四级NICU接受加巴喷丁治疗的患者进行的回顾性观察评估。分析了新生儿疼痛、躁动和镇静量表(N-PASS)评分的变化以及镇痛和镇静药物的需求,同时分析了加巴喷丁的剂量需求和不良反应。
在2012年1月至2015年11月期间,22例患者接受了加巴喷丁治疗并纳入本研究。加巴喷丁的平均起始剂量为10.2mg/kg/天,最大剂量可达25.5mg/kg/天。加巴喷丁治疗开始时的N-PASS评分中位数为3.1,开始使用加巴喷丁后,除5例患者外,所有记录的最后N-PASS评分均为0。使用加巴喷丁减少了镇痛或镇静药物的需求。该药物耐受性良好,只有1例患者对加巴喷丁有不良反应(即眼球震颤)。
加巴喷丁耐受性良好,且与疼痛评分降低相关。它的使用导致镇痛和镇静药物需求减少。加巴喷丁治疗似乎是治疗难治性疼痛和躁动的新生儿和婴儿的有效选择。