None listed
Conditions
Brief summary
The purpose of the trial is to conduct a prospective randomised controlled trial of Versajet hydrosurgery debridement (removal of necrotic/ non-viable tissue) of burns versus conventional tangential excisional debridement in paediatric patients. To date no trial has compared excisional debridement with Versajet hydrosurgery in paediatric burns patients. Our hypotheses is that 1.Versajet debridement leads to increased dermal preservation and accuracy of debridement 2.Versajet debridement is faster than conventional tangential excision in areas that are difficult to debride such as the hands, feet or perineum. 3.Graft healing time is equivalent following Versajet or classical blade debridement 4.Versajet debridement leads to improved outcomes post skin grafting such as hypertrophic scarring and contracture 5.Bacterial load is lower in the Versajet group following debridement
Interventions
The Versajet Hydrosurgery System is a tool that provides a high-pressure water jet capable of cutting tissue. It uses a high velocity sterile saline jet to cut/ debride the tissues and then draws tissue and fluid into a chamber via the Venturi effect created by the saline jet. This focused water jet passes parallel to the wound and is captured by an evacuator port which is located 8mm or 14mm from the nozzle. This jet of pressurised saline functions like a knife and the handpiece allows debridement and aspiration of debris to occur simultaneously. The Versajet system is currently utilised across many burns centres and at the Children’s Hospital at Westmead by the majority of burns surgeons and is considered a standard practice in selected cases. However, current literature regarding its clinical effectiveness (compared to the conventional tangential method of debridement using sharp excision) is scarce. The duration of debridement is dependent on the size (and depth) of the burn - approximately 10mins in burns of less than 5% TBSA. Some surgeons report that Versajet debridement is faster than conventional tangential excision in areas that are difficult to debride such as the hands, feet or perineum.
Sponsors
Study design
Eligibility
Inclusion criteria
All patients with a burn that requires debridement and undergoes acute skin grafting at The Children’s Hospital at Westmead (CHW) will be eligible for the study. Prior to entry into the study, written consent will be obtained by all patients or their guardians.
Exclusion criteria
Patients undergoing debridement without grafting, or with delayed grafting, will be excluded from the study. Patients with facial burns alone will be excluded from the study. Full thickness burns will be excluded from the study.