000 02651nam a22003857a 4500
008 200826s20202020 xxu||||| |||| 00| 0 eng d
022 _a1071-1007
024 _a10.1177/1071100720922220 [doi]
040 _aOvid MEDLINE(R)
099 _a32478578
245 _aA Consensus Statement on the Surgical Treatment of Charcot-Marie-Tooth Disease.
251 _aFoot & Ankle International. 41(7):870-880, 2020 07.
252 _aFoot Ankle Int. 41(7):870-880, 2020 07.
252 _zFoot Ankle Int. 41(7):870-880, 2020 Jul.
253 _aFoot & ankle international
260 _c2020
260 _fFY2021
265 _sppublish
266 _d2020-08-26
268 _aFoot & Ankle International. 41(7):870-880, 2020 Jul.
520 _aBACKGROUND: Charcot-Marie-Tooth (CMT) disease is a hereditary motor-sensory neuropathy that is often associated with a cavovarus foot deformity. Limited evidence exists for the orthopedic management of these patients. Our goal was to develop consensus guidelines based upon the clinical experiences and practices of an expert group of foot and ankle surgeons.
520 _aCONCLUSIONS: The group defined consensus terminology, agreed upon standardized templates for history and physical examination, and recommended a comprehensive approach to surgery. Early in the course of the disease, an orthopedic foot and ankle surgeon should be part of the care team. This consensus statement by a team of experienced orthopedic foot and ankle surgeons provides a comprehensive approach to the management of CMT cavovarus deformity.
520 _aLEVEL OF EVIDENCE: Level V, expert opinion.
520 _aMETHODS: Thirteen experienced, board-certified orthopedic foot and ankle surgeons and a neurologist specializing in CMT disease convened at a 1-day meeting. The group discussed clinical and surgical considerations based upon existing literature and individual experience. After extensive debate, conclusion statements were deemed "consensus" if 85% of the group were in agreement and "unanimous" if 100% were in support.
546 _aEnglish
650 _a*Charcot-Marie-Tooth Disease/su [Surgery]
650 _aConsensus
650 _aHumans
651 _aMedStar Union Memorial Hospital
657 _aJournal Article
700 _aGuyton, Greg
790 _aAn T, Brodsky J, Campbell J, Coetzee C, Conti S, Gonzalez T, Guyton G, Herrmann DN, Hunt K, Johnson J, McGarvey W, Michalski M, Noori N, Pfeffer GB, Pinzur M, Raikin S, Sangeorzan B, Younger A
856 _uhttps://dx.doi.org/10.1177/1071100720922220
_zhttps://dx.doi.org/10.1177/1071100720922220
942 _cART
_dArticle
999 _c5320
_d5320