Truffandier M-V, Perrot P, Duteille F
Service de chirurgie plastique et reconstructrice, centre des brûlés, hôpital Jean-Monnet, CHU de Nantes, 30, boulevard Jean-Monnet, 44093 Nantes cedex 01, France.
Service de chirurgie plastique et reconstructrice, centre des brûlés, hôpital Jean-Monnet, CHU de Nantes, 30, boulevard Jean-Monnet, 44093 Nantes cedex 01, France.
Ann Chir Plast Esthet. 2015 Aug;60(4):284-90. doi: 10.1016/j.anplas.2014.09.010.
Surgical treatment of congenital syndactylies is based on the creation of a new commissure - with a commissural flap - and on the management of fingers lateral faces - with mirror zigzag incisions. Lateral skin defects are covered by full-thickness skin graft. Since their discover 30 years ago, dermal substitutes applications have been enlarged. We have wandered if these technique could be interesting for the treatment of these lateral skin defects.
We have launched a monocentric and retrospective study with only one surgeon. The assessor and the operator were different. Included patients have a simple or complex congenital syndactyly, complete or not, associated with a syndrome or not. Children with a first web space syndactyly were excluded. Surgical treatment was performed with a dorsal commissural flap, with mirror incisions and with a lateral skin defects coverage by dermal substitute (Matriderm(©)) and split-thickness skin graft taken from the scalp. The initial assessment criterion was the quality of the scare measured by the OSAS score. Web creep (Whitney's scale) and time of surgery were two minor criteria.
Twenty commissures (11 children) have been included between 2008 and 2013. Fourteen complex syndactylies were noted. The average aftercare was equal to 2.7 years (0.5-5.5 years). Interventions were performed at the age of 1.8 years (0.5-4 years). Surgical time was equal to 44.6 min (22-95 min). Patients OSAS score was 11.9 (6-18). It was 12.2 (60-20) for complex forms and 11.9 (10-16) for simple forms. Graft weren't hairy. There was no complication on the donor site. Whitney's score was 1.2 (0-3) and three web spaces were reoperated.
We think that the use of dermal substitute Matriderm(©) is a new and serious alternative to treat congenital syndactylies. Results have to be confirmed by a new study which would compare this material to full-thickness skin graft, gold standard technique for these skin defects.
先天性并指的外科治疗基于通过连合瓣创建新的指蹼以及通过镜像锯齿状切口处理手指侧面。外侧皮肤缺损用全厚皮片覆盖。自30年前被发现以来,真皮替代物的应用范围不断扩大。我们一直在思考这些技术对于治疗这些外侧皮肤缺损是否会有帮助。
我们开展了一项单中心回顾性研究,只有一位外科医生参与。评估者和操作者不同。纳入的患者患有单纯或复杂的先天性并指,完全或不完全性,并指是否伴有综合征。第一蹼间隙并指的儿童被排除。手术治疗采用背侧连合瓣、镜像切口,并用真皮替代物(Matriderm(©))覆盖外侧皮肤缺损,同时取自头皮的中厚皮片进行移植。初始评估标准是通过OSAS评分测量的瘢痕质量。蹼缘增宽(惠特尼量表)和手术时间是两个次要标准。
2008年至2013年间纳入了20个指蹼(11名儿童)。记录到14例复杂并指。平均随访时间为2.7年(0.5 - 5.5年)。手术在1.8岁(0.5 - 4岁)时进行。手术时间为44.6分钟(22 - 95分钟)。患者的OSAS评分为11.9(6 - 18)。复杂型为12.2(6 - 20),简单型为11.9(10 - 16)。移植皮片无毛发。供区无并发症。惠特尼评分为1.2(0 - 3),3个蹼间隙进行了再次手术。
我们认为使用真皮替代物Matriderm(©)是治疗先天性并指的一种新的且重要的替代方法。结果必须通过一项新的研究来证实,该研究将这种材料与全厚皮片(这些皮肤缺损的金标准技术)进行比较。