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临床试验/NCT03081026
NCT03081026已完成不适用

Transphyseal Vs. Physeal Sparing ACL Reconstruction in Skeletally Immature Patients: Risk of Subsequent Lower Extremity Growth Deformity

Duke University1 个研究点 分布在 1 个国家目标入组 49 人开始时间: 2017年5月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
49
试验地点
1
主要终点
Limb Angular alignment

研究概览

简要总结

To assess the risk of lower extremity angular growth deformity following anterior cruciate ligament (ACL) reconstructions in young patients who are not yet skeletally mature. The study will compare two surgical techniques (physeal sparing vs transphyseal).

详细描述

Background & Significance: In the adult population, the vast majority of ACL reconstructions are performed by drilling femoral and tibial bone tunnels. Because these patients have achieved physeal closure by the time of surgery, there is no risk of angular growth deformity when creating tibial and femoral tunnels. However, in the pediatric patient with open tibial and femoral physes, there is concern that drilling across the physes using standard tunnels may cause physeal injury with resultant angular deformity. Other surgical techniques have been described that allow the graft to be placed without drilling tunnels across the tibial and femoral physes but there is debate regarding whether or not these "physeal sparing" techniques are as effective as the transphyseal tunnel positions. Drilling the tunnels in the epiphysis to avoid the physis is a common "physeal sparing" technique. It is debated whether this technique could also cause growth disturbances. Given the increasing number of pediatric ACL injuries and that 95% of patients age 12 or less have open physes and that 94% of patients age 14 or greater have closed physes, this topic is of significant interest. Similar studies have been conducted but most have been either small and underpowered or have included older adolescent patients. At Duke Sports Sciences Institute, we have a sizable population of patients age 16 or less who have undergone ACL reconstruction with both transphyseal and all epiphyseal techniques. This provides a unique opportunity to analyze and compare these two groups with respect to clinical outcome and the incidence of growth disturbance or angular deformity

Design & Procedures: The investigator will conduct a review of medical records of seven providers at a single site institution to determine the subject population. Specifically, the investigator will look for patients who had an ACL reconstruction between the ages of 6-16 after January 1, 2005. The investigator will confirm in the medical record and in pre-operative radiographs that the growth plates were open at the time of surgery. Only subjects with open physeal will be enrolled in the study and they will be placed in 3 cohorts: Ages less than 12, 12-13, and 14 - 16. Subjects will be contacted by phone by a member of the team and asked to return to Duke Sports Sciences Institute to participate in the study. Upon arrival to clinic, subjects will be consented for the study and undergo a full physical exam - specifically targeting the gait and range of motion, as well as the Lachman, Anterior Drawer and Pivot Shift maneuvers to assess stability and functionality of the graft. In addition, they will complete a questionnaire designed to elicit patient satisfaction and level of activity/sports participation after the initial recovery period. Bilateral hip to ankle radiographs will be taken of each subject. These radiographs will be analyzed to assess for any angular deformity between the surgical and non-surgical leg. In addition, baseline knee x-rays will be reviewed for determination of skeletal maturity at time of injury/surgery. Data will be organized according to patients who underwent transphyseal reconstruction and patients who underwent physeal sparing reconstruction and separated into the corresponding age group. Comparisons will be made between the two surgical techniques based on the following criteria:

  • Patient satisfaction and return to function
  • Graft stability
  • Angular deformity
  • Skeletal maturity at the time of surgery

Study Interventions: Subjects will undergo physical examination (gait, inspections, range of motion and instability testing) and completion of an outcome tool survey (IKDC score/PediIKDC, VAS, Marx, and ACL-RSIsurvey). Subjects will undergo bilateral hip to ankle radiographic imaging to assess for growth deformity. Subjects will also be asked to give their permission to review their medical record and imaging pertinent to the knees and knee surgery.

Data Analysis & Statistical Considerations: Patient's data will be collected in a database program, indexed initially by medical record number. After case collection, case numbers will be applied and medical record numbers stripped from the data. The code linking medical record number to case number will be kept in a locked file with access limited to primary investigator.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Cross Sectional

入排标准

年龄范围
6 Years 至 16 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Subjects will be identified by reviewing medical records that include a procedure code for ACL reconstruction in patients between the ages of 6-16 at the time of surgery. Patients meeting the inclusion criteria will be contacted by phone and invited to participate in the study. A key personnel member who is part of the principal investigator's research staff will make phone contact with the patient. The study will be explained and any questions that the subject may have will be answered at that time. If the subject agrees to participate in the study, he/she will make an appointment at that time to come in to be consented and participate in the study and for imaging and testing at Duke Sports Sciences Institute.

排除标准

  • Pregnant Females

结局指标

主要结局

Limb Angular alignment

时间窗: Clinic visit, approximately 1 hour

Bilateral hip to ankle radiographs measurements

Limb length discrepancy

时间窗: Clinic visit, approximately 1 hour

Bilateral hip to ankle radiographs measurements.

次要结局

  • Range of motion measurements(Clinic visit, approximately 1 hour)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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