Development of an enhanced recovery after surgery program for pediatric solid tumors

被引:2
作者
Mansfield, Sara A. [1 ,2 ]
Kotagal, Meera [3 ]
Hartman, Stephen [3 ]
Murphy, Andrew J. [1 ]
Davidoff, Andrew M. [1 ]
Anghelescu, Doralina L. [4 ]
Mecoli, Marc [5 ]
Cost, Nicholas [6 ]
Hogan, Brady [6 ]
Rove, Kyle O. [6 ]
机构
[1] St Jude Childrens Res Hosp, Dept Surg, Memphis, TN USA
[2] Nationwide Childrens Hosp, Dept Pediat Surg, Columbus, OH USA
[3] Cincinnati Childrens Hosp Med Ctr, Dept Pediat Surg, Cincinnati, OH USA
[4] St Jude Childrens Res Hosp, Dept Pediat Med, Div Anesthesiol, Memphis, TN USA
[5] Cincinnati Childrens Hosp Med Ctr, Div Anesthesiol, Cincinnati, OH USA
[6] Childrens Hosp Colorado, Dept Urol, Aurora, CO 80045 USA
来源
FRONTIERS IN SURGERY | 2024年 / 11卷
关键词
pediatric oncology; enhanced recovery after surgery; enhance recovery pathways; pediatric surgical oncology; solid tumors; SURGICAL COMPLICATIONS; RISK;
D O I
10.3389/fsurg.2024.1393857
中图分类号
R61 [外科手术学];
学科分类号
摘要
Introduction Enhanced recovery after surgery (ERAS) is an evidence-based, multi-modal approach to decrease surgical stress, expedite recovery, and improve postoperative outcomes. ERAS is increasingly being utilized in pediatric surgery. Its applicability to pediatric patients undergoing abdominal tumor resections remains unknown. Methods and Analysis A group of key stakeholders adopted ERAS principles and developed a protocol suitable for the variable complexity of pediatric abdominal solid tumor resections. A multi-center, prospective, propensity-matched case control study was then developed to evaluate the feasibility of the protocol. A pilot-phase was utilized prior to enrollment of all patients older than one month of age undergoing any abdominal, retroperitoneal, or pelvic tumor resections. The primary outcome was 90-day complications per patient. Additional secondary outcomes included: ERAS protocol adherence, length of stay, time to administration of adjuvant chemotherapy, readmissions, reoperations, emergency room visits, pain scores, opioid usage, and differences in Quality of Recovery 9 scores. Ethics and Dissemination Institutional review board approval was obtained at all participating centers. Informed consent was obtained from each participating patient. The results of this study will be presented at pertinent society meetings and published in peer-reviewed journals. We expect the results will inform peri-operative care for pediatric surgical oncology patients and provide guidance on initiation of ERAS programs. We anticipate this study will take four years to meet accrual targets and complete follow-up. Trial Registration Number NCT04344899.
引用
收藏
页数:9
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