The study design is a prospective observational study examining the medical record for operative time, intraoperative blood loss, intraoperative standard care narcotic use, postoperative standard analgesic use, postoperative complication rate for hemorrhage and dehydration as well as incidence of doctor visits in the postoperative period. a questionnaire will be completed by parent recording pain level, standard pain medication use and return to regular diet,. Primary endpoint will be the postoperative screening contact or visit at 2-4 weeks with return of completed questionnaire. The secondary endpoint would be return to the operating room or eR for control of hemorrhage.