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1.
Wound Repair Regen ; 28(3): 375-384, 2020 05.
Article in English | MEDLINE | ID: mdl-32022363

ABSTRACT

The clinical effectiveness and scar quality of the randomized controlled trial comparing enzyme alginogel with silver sulfadiazine (SSD) for treatment of partial thickness burns were previously reported. Enzyme alginogel did not lead to faster wound healing (primary outcome) or less scar formation. In the current study, the health-related quality of life (HRQoL), costs, and cost-effectiveness of enzyme alginogel compared with SSD in the treatment of partial thickness burns were studied. HRQoL was evaluated using the Burn Specific Health Scale-Brief (BSHS-B) and the EQ-5D-5L questionnaire 1 week before discharge and at 3, 6, and 12 months postburn. Costs were studied from a societal perspective (health care and nonhealth-care costs) for a follow-up period of 1 year. A cost-effectiveness analysis was performed using cost-effectiveness acceptability curves and comparing differences in societal costs and Quality Adjusted Life Years (QALYs) at 1 year postburn. Forty-one patients were analyzed in the enzyme alginogel group and 48 patients in the SSD group. None of the domains of BSHS-B showed a statistically significant difference between the treatment groups. Also, no statistically significant difference in QALYs was found between enzyme alginogel and SSD (difference -0.03; 95% confidence interval [CI], -0.09 to 0.03; P = .30). From both the health care and the societal perspective, the difference in costs between enzyme alginogel and SSD was not statistically significant: the difference in health-care costs was €3210 (95% CI, €-1247 to €7667; P = .47) and in societal costs was €3377 (95% CI €-6229 to €12 982; P = .49). The nonsignificant differences in costs and quality-adjusted life-years in favor of SSD resulted in a low probability (<25%) that enzyme alginogel is cost-effective compared to SSD. In conclusion, there were no significant differences in quality of life between both treatment groups. Enzyme alginogel is unlikely to be cost-effective compared with SSD in the treatment of partial thickness burns.


Subject(s)
Alginates/therapeutic use , Anti-Infective Agents, Local/therapeutic use , Burns/economics , Burns/therapy , Glucose Oxidase/therapeutic use , Lactoperoxidase/therapeutic use , Polyethylene Glycols/therapeutic use , Quality of Life , Silver Sulfadiazine/therapeutic use , Adult , Aged , Alginates/economics , Anti-Infective Agents, Local/economics , Burns/pathology , Cost-Benefit Analysis , Drug Combinations , Female , Glucose Oxidase/economics , Humans , Lactoperoxidase/economics , Male , Middle Aged , Polyethylene Glycols/economics , Silver Sulfadiazine/economics , Time Factors , Treatment Outcome , Wound Healing
2.
Trials ; 17(1): 122, 2016 Mar 05.
Article in English | MEDLINE | ID: mdl-26945575

ABSTRACT

BACKGROUND: Partial thickness burns are painful, difficult to manage and can have a negative effect on quality of life through scarring, permanent disfigurement and loss of function. The aim of burn treatment in partial thickness burns is to save lives, stimulate wound healing by creating an optimumly moist wound environment, to have debriding and analgesic effects, protect the wound from infection and be convenient for the patient and caregivers. However, there is no consensus on the optimal treatment of partial thickness wounds. Flaminal® and Flamazine® are two standard treatment options that provide the above mentioned properties in burn treatment. Nevertheless, no randomized controlled study has yet compared these two common treatment modalities in partial thickness burns. Thus, the aim of this study is to evaluate the clinical effectiveness, quality of life and cost-effectiveness of Flaminal® versus Flamazine® in the treatment of partial thickness burns. METHODS/DESIGN: In this two-arm open multi-center randomized controlled trial, 90 patients will be randomized between Flaminal® and Flamazine® and followed for 12 months. The study population will consist of competent or temporarily non-competent (because of sedation and/or intubation) patients, 18 years of age or older, with acute partial thickness burns and a total body surface area (TBSA) of less than 30 %. The main study outcome is time to complete re-epithelialization (greater than 95 %). Secondary outcome measures include need for grafting, wound colonization/infection, number of dressing changes, pain and anxiety, scar formation, health-related quality of life (HRQoL), and costs. DISCUSSION: This study will contribute to the optimal treatment of patients with partial thickness burn wounds and will provide evidence on the (cost-)effectiveness and quality of life of Flaminal® versus Flamazine® in the treatment of partial thickness burns. TRIAL REGISTRATION: Netherlands Trial Register NTR4486 , registered on 2 April 2014.


Subject(s)
Alginates/economics , Alginates/therapeutic use , Anti-Infective Agents, Local/economics , Anti-Infective Agents, Local/therapeutic use , Burns/drug therapy , Burns/economics , Drug Costs , Glucose Oxidase/economics , Glucose Oxidase/therapeutic use , Lactoperoxidase/economics , Lactoperoxidase/therapeutic use , Polyethylene Glycols/economics , Polyethylene Glycols/therapeutic use , Quality of Life , Silver Sulfadiazine/economics , Silver Sulfadiazine/therapeutic use , Skin/drug effects , Wound Healing/drug effects , Alginates/adverse effects , Anti-Infective Agents, Local/adverse effects , Burns/complications , Burns/psychology , Cicatrix/etiology , Cicatrix/therapy , Clinical Protocols , Cost-Benefit Analysis , Drug Combinations , Glucose Oxidase/adverse effects , Humans , Lactoperoxidase/adverse effects , Netherlands , Pain/etiology , Polyethylene Glycols/adverse effects , Re-Epithelialization/drug effects , Research Design , Silver Sulfadiazine/adverse effects , Skin/pathology , Skin Transplantation , Time Factors , Treatment Outcome , Wound Infection/microbiology , Wound Infection/therapy
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