van den Eijnden Maria Hendrina Antoinette, de Kleine Ruben H, Verkade Henkjan J, Wilde Jim C H, Peeters Paul M J G, Hulscher Jan B F
Department of Pediatric Surgery, University Medical Centre Groningen, Groningen, The Netherlands.
Department of Hepatobiliary Surgery and Liver Transplantation, University Medical Center Groningen, Groningen, The Netherlands.
Eur J Pediatr Surg. 2015 Oct;25(5):441-8. doi: 10.1055/s-0034-1387947. Epub 2014 Oct 26.
Choledochal malformation (CM) is a rare medical condition of which 80% are diagnosed in pediatric patients. There are several important controversies regarding diagnostic workup, management, and follow-up in these pediatric patients. To assess preferences and practices of Dutch pediatric surgeons regarding the diagnostic procedures, management, and follow-up of children with CM we conducted an electronic survey.
A questionnaire was sent to all the pediatric surgeons working in the academic centers and the only community hospital with a pediatric surgery service. The questionnaire included, items regarding incidence, diagnostic workup, interval between diagnosis and surgery, surgical techniques, and follow-up. We also assessed whether personal exposure influenced the preferences and practices.
Overall 22 out of the 31 (71%) Dutch pediatric surgeons returned the questionnaire. Total 15 out of 22 (68%) encountered CM up to 2 times/y, whereas 7 out of 22 (32%) encountered it more than 2 times/y. Indications for surgery were significantly different between surgeons who encountered CM > 2 time/y versus those who did not: 6/6 (100%) of surgeons encountering CM > 2 times/y considered the presence of an asymptomatic CM an indication for surgery versus 5/14 (36%) of the pediatric surgeons who encountered a CM up to 2 times/y (p = 0.01). Overall 12 out of the 22 (55%) respondents preferred surgery between 6 months and 2 years of age. The amount of exposure did not differ in preferred age at surgery or surgical technique. In the symptomatic child 10/22 (45%) of respondents preferred surgery within 3 months. Overall 7/22 (32%) favored laparoscopic resection. Hepaticojejunostomy with Roux-en-Y reconstruction was the preferred reconstruction for all the respondents. One-third stated that they never performed a parenchyma resection. Follow-up was limited to 10 years in almost half of the respondents.
Dutch pediatric surgeons demonstrate a wide variety of opinions regarding diagnostic workup, treatment, and follow-up of CM. While most surgeons encounter CM up to 2 times/y, there is an association between exposure and several of the outcome parameters. Some of the answers are not in line with the expert opinion. This demonstrates that there is a need for evidence-based (inter)national guidelines regarding the diagnostic approach, management, and follow-up.
胆管畸形(CM)是一种罕见的病症,80%在儿科患者中被诊断出来。在这些儿科患者的诊断检查、治疗及随访方面存在一些重要争议。为评估荷兰儿科外科医生对CM患儿诊断程序、治疗及随访的偏好和做法,我们开展了一项电子调查。
向在学术中心及唯一设有儿科手术服务的社区医院工作的所有儿科外科医生发送了一份问卷。问卷包括有关发病率、诊断检查、诊断与手术间隔时间、手术技术及随访的项目。我们还评估了个人经验是否会影响偏好和做法。
31名荷兰儿科外科医生中有22名(71%)回复了问卷。22名医生中共有15名(68%)每年遇到CM不超过2次,而22名中有7名(32%)每年遇到CM超过2次。每年遇到CM超过2次的外科医生与未超过2次的医生在手术指征上有显著差异:每年遇到CM超过2次的外科医生中有6/6(100%)认为无症状CM是手术指征,而每年遇到CM不超过2次的儿科外科医生中这一比例为5/14(36%)(p = 0.01)。22名受访者中共有12名(55%)倾向于在6个月至2岁之间进行手术。经验多少在手术首选年龄或手术技术方面并无差异。对于有症状的患儿,10/22(45%)的受访者倾向于在3个月内进行手术。总体而言,7/22(32%)倾向于腹腔镜切除术。所有受访者首选的重建方式是 Roux-en-Y 重建的肝空肠吻合术。三分之一的人表示他们从未进行过实质切除术。近一半的受访者将随访限制在10年。
荷兰儿科外科医生在CM的诊断检查、治疗及随访方面表现出广泛的意见分歧。虽然大多数外科医生每年遇到CM不超过2次,但经验与一些结果参数之间存在关联。一些答案与专家意见不一致。这表明需要基于证据的(国际)指南来指导诊断方法、治疗及随访。