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先天性肢体长度差异中的牵张成骨:综述

Distraction osteogenesis in congenital limb length discrepancy: a review.

作者信息

Maffuli N, Fixsen J A

机构信息

Department of Orthopaedic Surgery, University of Aberdeen Medical School, UK.

出版信息

J R Coll Surg Edinb. 1996 Aug;41(4):258-64.

PMID:8772079
Abstract

This paper reviews the technique of callotasis used to correct limb length discrepancy due to congenital causes. Many more lower than upper limb lengthening procedures have been reported. Despite the low complication rate reported by the originators of the technique, patients undergoing limb lengthening because of congenital problems are at significant risk of pin tract sepsis, joint contracture, nerve palsies, angular deformities and fracture through the regenerate bone. A minority of studies focus specifically on limb lengthening for congenital defects. Most series simply include some congenital patients, but it is difficult to retrieve the data, and to generalize from them. The amount of lengthening with an acceptable complication rate should not exceed 25%; of the initial bone length. Even using circular frames with small pins, practically all patients may be expected to develop at least one complication each, ranging from pin tract infection to the necessity of carrying out additional unplanned operative procedures either during or after the treatment period. The prevalence of major complications seems to be correlated with the complexity and the duration of the treatment. The functional outcome and the psychological problems associated with a lengthy procedure, which may require long periods of repeated hospitalization, have only rarely been studied. However, it appears that prolonged strength loss is frequent, and that significant psychological morbidity is experienced. Patients and their families should be counselled before and during the procedure on these lesser known aspects of callotasis lengthening.

摘要

本文回顾了用于纠正先天性原因导致的肢体长度差异的骨痂延长术。据报道,下肢延长手术比上肢延长手术少得多。尽管该技术的发明者报告的并发症发生率较低,但因先天性问题接受肢体延长手术的患者仍面临着针道感染、关节挛缩、神经麻痹、成角畸形以及再生骨骨折等重大风险。少数研究专门关注先天性缺陷的肢体延长。大多数系列研究只是简单地纳入了一些先天性患者,但很难从中检索数据并进行归纳总结。在可接受的并发症发生率情况下,延长的长度不应超过初始骨长度的25%。即使使用带有小针的环形外固定架,实际上所有患者预计至少都会出现一种并发症,从针道感染到在治疗期间或之后需要进行额外的非计划手术。主要并发症的发生率似乎与治疗的复杂性和持续时间相关。对于可能需要长时间反复住院的漫长手术所带来的功能结果和心理问题,很少有人进行研究。然而,似乎长期力量丧失很常见,并且患者会经历严重的心理疾病。在手术前和手术期间,应就骨痂延长术这些鲜为人知的方面对患者及其家属进行咨询。

相似文献

1
Distraction osteogenesis in congenital limb length discrepancy: a review.先天性肢体长度差异中的牵张成骨:综述
J R Coll Surg Edinb. 1996 Aug;41(4):258-64.
2
[Femoral lengthening by callotasis. A study of a series of 79 cases in children and adolescents].[骺骨干延长术。对79例儿童和青少年的系列研究]
Rev Chir Orthop Reparatrice Appar Mot. 1995;81(2):147-56.
3
A review of 240 patients undergoing distraction osteogenesis for congenital post-traumatic or postinfective lower limb length discrepancy.对240例因先天性创伤后或感染后下肢长度不等而接受牵张成骨术的患者进行的一项回顾性研究。
J Am Coll Surg. 1996 May;182(5):394-402.
4
Callotasis lengthening: a review of some technical aspects.骨痂延长术:一些技术方面的综述
Bull Hosp Jt Dis. 1996;54(4):249-54.
5
[The fate of children undergoing bone lengthening in congenital hypoplasia of the legs].
Rev Chir Orthop Reparatrice Appar Mot. 1990;76(1):1-7.
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Recent advances in limb lengthening. Part I: Clinical advances.
Orthop Rev. 1992 Mar;21(3):307-14.
7
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Clin Orthop Relat Res. 1993 Jun(291):236-45.
8
Femoral lengthening by the Wagner method.
Clin Orthop Relat Res. 1990 Jan(250):154-9.
9
Limb lengthening by callotasis for children and adolescents. Early experience.儿童和青少年骺牵张肢体延长术:早期经验
Clin Orthop Relat Res. 1990 Jan(250):105-11.
10
Fractures after Wagner limb lengthening.
J Pediatr Orthop. 1992 Jan;12(1):20-4.

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2
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Lengthening in Congenital Femoral Deficiency: A Comparison of Circular External Fixation and a Motorized Intramedullary Nail.先天性股骨缺损的延长治疗:环形外固定与电动髓内钉的比较
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Eur J Orthop Surg Traumatol. 2014 Jul;24(5):693-8. doi: 10.1007/s00590-013-1261-7. Epub 2013 Jun 23.
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"Asymmetric scalloping of the regenerate": a radiological sign of pseudoaneurysm in distraction osteogenesis.“再生骨的不对称扇贝样改变”:牵张成骨中假性动脉瘤的影像学征象
Strategies Trauma Limb Reconstr. 2011 Nov;6(3):159-62. doi: 10.1007/s11751-011-0121-4. Epub 2011 Nov 18.
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