Busse Jennifer, Louie Aaron, Crotty Jennifer, Lin Albert, Muratova Zarema, Malka Matan, Givens Ritt, Roye Benjamin, Vitale Michael, Schechter William
Department of Anesthesiology, Columbia University Irving Medical Center, New York, NY, USA.
Department of Orthopedics, Columbia University Irving Medical Center, New York, NY, USA.
J Pediatr Soc North Am. 2025 Mar 14;11:100174. doi: 10.1016/j.jposna.2025.100174. eCollection 2025 May.
Significant postoperative nausea and vomiting (PONV) in pediatric patients undergoing posterior spinal fusion is common and limits recovery, prolonging hospital stay. Fosaprepitant is a long-acting antiemetic and works by blocking substance P binding to the neurokinin-1 (NK) receptor. There is evidence that its perioperative use substantially reduces PONV in adults, but there is a dearth of literature on its use in pediatric PONV. We seek to elucidate whether a postoperative dose of fosaprepitant in pediatric posterior instrumentation and fusion (PSIF) patients decreases PONV, thus improving recovery and decreasing the length of hospital stay.
This is a retrospective chart review of 173 pediatric patients with idiopathic scoliosis undergoing PSIF. The anesthetic methodology was standardized among both groups. The cohort was divided into two groups according to the use of fosaprepitant intraoperatively (or within four hours postoperatively) or no use. We examined patient characteristics, fosaprepitant dose, incidence of PONV, time to transition from parenteral to oral opioids, and length of hospital stay.
78 (45%) patients received fosaprepitant and 95 (55%) did not. There were no statistically significant differences between groups based on demographics or intraoperative management. No significant difference was found in the incidence of PONV between the groups, but there was a reduction in the number of rescue antiemetics required and a quicker transition from parenteral to oral opioids in the fosaprepitant group. There was also a significantly decreased length of stay.
While fosaprepitant did not significantly decrease PONV in pediatric PSIF patients, it was associated with decreased use of additional antiemetics. The patients also demonstrated a more rapid transition to oral from parenteral opioids and a shorter length of hospital stay. A larger study may show a statistically significant reduction in PONV in patients who received fosaprepitant. Future studies are needed to elucidate the optimal dose and timing needed to treat PONV in pediatrics.
(1)Spinal fusion surgery patients are at risk of having significant postoperative nausea and vomiting.(2)Fosaprepitant is an effective agent to treat postoperative nausea and vomiting in adults, but has not been extensively studied in pediatrics for this purpose.
The level of evidence is a 3 as it is a cohort study looking at the relationship between an exposure and an outcome.
接受后路脊柱融合术的儿科患者术后出现严重恶心呕吐(PONV)很常见,这会限制恢复,延长住院时间。福沙匹坦是一种长效止吐药,通过阻断P物质与神经激肽-1(NK)受体的结合发挥作用。有证据表明,其围手术期使用可大幅降低成人的PONV,但关于其在儿科PONV中的应用的文献较少。我们试图阐明,在儿科后路器械固定和融合术(PSIF)患者中术后给予福沙匹坦是否能降低PONV,从而改善恢复情况并缩短住院时间。
这是一项对173例接受PSIF的特发性脊柱侧弯儿科患者的回顾性病历审查。两组的麻醉方法均标准化。根据术中(或术后4小时内)是否使用福沙匹坦将队列分为两组。我们检查了患者特征、福沙匹坦剂量、PONV发生率、从胃肠外给药过渡到口服阿片类药物的时间以及住院时间。
78例(45%)患者接受了福沙匹坦,95例(55%)未接受。基于人口统计学或术中管理,两组之间无统计学显著差异。两组之间PONV发生率无显著差异,但福沙匹坦组所需的补救性止吐药数量减少,从胃肠外给药过渡到口服阿片类药物的速度更快。住院时间也显著缩短。
虽然福沙匹坦在儿科PSIF患者中并未显著降低PONV,但它与额外止吐药的使用减少有关。患者从胃肠外阿片类药物过渡到口服药物的速度也更快,住院时间更短。一项更大规模的研究可能会显示接受福沙匹坦治疗的患者的PONV有统计学显著降低。未来需要进行研究以阐明治疗儿科PONV所需的最佳剂量和时机。
(1)脊柱融合手术患者有发生严重术后恶心呕吐的风险。(2)福沙匹坦是治疗成人术后恶心呕吐的有效药物,但尚未针对此目的在儿科进行广泛研究。
证据水平为3级,因为这是一项观察暴露与结局之间关系的队列研究。