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Comparison of 2 Fasciotomes for Treatment of Patients With Chronic Exertional Compartment Syndrome of the Anterior Leg.
de Bruijn, Johan A; van Zantvoort, Aniek P M; Hundscheid, Henricus P H; Hoogeveen, Adwin R; van Eerten, Percy; Teijink, Joep A W; Scheltinga, Marc R.
Afiliación
  • de Bruijn JA; Department of Surgery, Máxima Medical Center, Veldhoven, the Netherlands.
  • van Zantvoort APM; Department of Surgery, Máxima Medical Center, Veldhoven, the Netherlands.
  • Hundscheid HPH; Department of Surgery, Máxima Medical Center, Veldhoven, the Netherlands.
  • Hoogeveen AR; Department of Sports Medicine, Máxima Medical Center, Veldhoven, the Netherlands.
  • van Eerten P; Department of Surgery, Máxima Medical Center, Veldhoven, the Netherlands.
  • Teijink JAW; Department of Surgery, Catherina Hospital, Eindhoven, the Netherlands.
  • Scheltinga MR; Department of Epidemiology, CAPHRI Research School, Maastricht University, Maastricht, the Netherlands.
Orthop J Sports Med ; 9(11): 23259671211051358, 2021 Nov.
Article en En | MEDLINE | ID: mdl-34888390
ABSTRACT

BACKGROUND:

Chronic exertional compartment syndrome (CECS) of the anterior leg compartment (ant-CECS) is frequently treated with a minimally invasive fasciotomy. Several operative techniques and operative devices exist, but none have been compared in a systematic and randomized manner.

PURPOSE:

To compare efficacy, safety, and postoperative pain of a novel operative device (FascioMax fasciotome) with a widely accepted device created by Due and Nordstrand (Due fasciotome) during a minimally invasive fasciotomy for ant-CECS. STUDY

DESIGN:

Randomized controlled trial; Level of evidence, 2.

METHODS:

Patients with bilateral isolated ant-CECS between October 2013 and April 2018 underwent a minimally invasive fasciotomy using the FascioMax fasciotome in 1 leg and the Due fasciotome in the contralateral leg in a single operative session. Symptom reduction at 3 to 6 months and >1 year, postoperative pain within the first 2 weeks, peri- and postoperative complications, and ability to regain sports were assessed using diaries, physical examination, and timed questionnaires.

RESULTS:

Included in the study were 50 patients (66% female; median age, 22 years [range, 18-65 years]). No differences between the devices were found in terms of perioperative complications (both had none), minor postoperative complications including hematoma and superficial wound infection (overall complication rate FascioMax, 8% vs Due, 6%), or reduction of CECS-associated symptoms at rest and during exercise. At long-term follow-up (>1 year), 82% of the patients were able to regain their desired type of sport, and 67% (33/49) were able to exercise at a level that was comparable with or higher than before their CECS-associated symptoms started.

CONCLUSION:

Both the FascioMax and the Due performed similarly in terms of efficacy, safety, and levels of pain within the first 2 weeks postoperatively. REGISTRATION NL4274; Netherlands Trial Register.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Clinical_trials Idioma: En Revista: Orthop J Sports Med Año: 2021 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Clinical_trials Idioma: En Revista: Orthop J Sports Med Año: 2021 Tipo del documento: Article País de afiliación: Países Bajos
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