Black Sheena R, Kwon Michael S, Cherkashin Alexander M, Samchukov Mikhail L, Birch John G, Jo Chan-Hee
Department of Orthopedics, Texas Scottish Rite Hospital for Children, 2222 Welborn Street, Dallas, TX 75219. E-mail address for J.G. Birch:
St. Christopher's Hospital for Children, 3601 A Street, Philadelphia, PA 19134.
J Bone Joint Surg Am. 2015 Sep 2;97(17):1432-40. doi: 10.2106/JBJS.N.00932.
Circular external fixation for limb-lengthening is associated with frequent and numerous complications. Intramedullary lengthening devices represent a potential advance in limb-lengthening. The purpose of this study was to compare the outcomes of femoral lengthening in pediatric patients treated by either circular external fixation or a motorized intramedullary nail.
All patients with a diagnosis of congenital femoral deficiency who had undergone femoral lengthening with either circular external fixation or a motorized intramedullary nail were identified. The motorized intramedullary nail (FITBONE) was used with approval of the U.S. Food and Drug Administration on an individual compassionate-use basis.
Fourteen skeletally mature patients underwent fourteen femoral lengthening sessions using circular external fixation, and thirteen patients underwent fifteen lengthening sessions using the motorized nail. The amount lengthened was similar, with a mean of 4.8 cm (range, 1.0 to 7.4 cm) in the circular fixation group and 4.4 cm (range, 1.5 to 7.0 cm) in the motorized nail group. Complications occurred in all lengthening sessions in all fourteen patients managed with the circular external fixation and in 73% of fifteen lengthening sessions in the thirteen patients managed with the motorized nail. The circular external fixation group averaged 2.36 complications per lengthening session compared with 1.2 per session in the motorized nail group. Twenty-nine percent of the circular fixation group failed to achieve a lengthening goal of at least 4 cm compared with 27% of the motorized nail group who failed to reach the goal. Eight patients had undergone eleven femoral lengthening sessions with circular external fixation prior to undergoing ten lengthening sessions by motorized nail. These patients had a comparable rate of complications with both types of lengthening, but the total number of complications averaged 2.6 per lengthening session with circular external fixation compared with 1.6 per lengthening session with the motorized nail.
A decreased number of complications was noted with use of a motorized intramedullary nail compared with circular external fixation in pediatric patients undergoing femoral lengthening for congenital femoral deficiency.
Therapeutic Level III. See Instructions for Authors for a complete description of levels of evidence.
肢体延长的环形外固定常伴有频繁且众多的并发症。髓内延长装置代表了肢体延长领域的一项潜在进展。本研究的目的是比较采用环形外固定或电动髓内钉治疗的小儿患者股骨延长的结果。
确定所有诊断为先天性股骨缺如且接受过环形外固定或电动髓内钉股骨延长治疗的患者。电动髓内钉(FITBONE)是在美国食品药品监督管理局批准下基于个体同情使用的情况使用的。
14例骨骼成熟患者使用环形外固定进行了14次股骨延长手术,13例患者使用电动髓内钉进行了15次延长手术。延长的长度相似,环形固定组平均延长4.8厘米(范围1.0至7.4厘米),电动髓内钉组平均延长4.4厘米(范围1.5至7.0厘米)。在接受环形外固定治疗的所有14例患者的所有延长手术中均出现并发症,在接受电动髓内钉治疗的13例患者的15次延长手术中有73%出现并发症。环形外固定组每次延长手术平均有2.36例并发症,而电动髓内钉组每次手术为1.2例。环形固定组有29%未能达到至少4厘米的延长目标,电动髓内钉组有27%未能达到该目标。8例患者在接受电动髓内钉进行10次延长手术之前,曾使用环形外固定进行过11次股骨延长手术。这些患者两种延长方式的并发症发生率相当,但环形外固定每次延长手术的并发症总数平均为2.6例,而电动髓内钉每次延长手术为1.6例。
对于因先天性股骨缺如接受股骨延长的小儿患者,与环形外固定相比,使用电动髓内钉并发症数量减少。
治疗性三级。有关证据级别的完整描述,请参阅作者指南。