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AFRICAN RESEARCH NEXUS

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Tibia fracture management in low-resource settings using the External Fixation and Traction Device of the Guinean Military Health Service

Orthopaedics and Traumatology: Surgery and Research, Volume 108, No. 7, Article 103377, Year 2022

Introduction: The authors analyzed results over a 7-year period for a locally manufactured external fixation and traction device (EFTD) used in tibial fracture. Three models were used, depending on the medical and technological context of the healthcare structure in question. The aim of the present study was to reports results for tibial fracture treated by EFTD in low-resource settings. Materials and methods: A multicenter observational study was conducted for the period 2008-2015 in a series of 34 tibial fractures (22 right, 12 left, with 1 bilateral) in 33 young adults (28 male, 5 female; mean age, 42.2 years). Nineteen were closed fractures and 15 open. The 11 recent open fractures comprised 2 Cauchoix-Duparc type I, 3 type II and 6 type III; the 4 older open fractures were infected. Four patients were lost to follow-up. Results: Seventeen of the patients with closed fracture had very good results, in 75% (6/8) of shaft fractures and 55.55% (5/9) of complex metaphyseal-epiphyseal fractures. In infected fractures older than 48 h, there were good results in 25% of cases. In recent open fractures, there were 100% (2/2), 66.6% (2/3) and 20% (1/5) good results for types I, II and III respectively. Five patients showed malunion, well-tolerated functionally. Mean time to bone healing was 16 weeks (range, 12-72 weeks). Conclusion: In developing countries, the pitfall in treating open fractures is delayed surgery due to patients’ socioeconomic situation and to underequipment. The EFTD is a promising technique, readily available at low cost, easy to implement and with minimal iatrogenesis. Level of evidence: IV, prospective observational study.
Statistics
Citations: 7
Authors: 7
Affiliations: 4
Identifiers
Research Areas
Health System And Policy
Violence And Injury
Study Design
Cohort Study
Participants Gender
Male
Female