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Mucormycosis following burn injuries: A systematic review
Affiliation:1. Keck School of Medicine, University of Southern California, Los Angeles, CA, United States;2. Division of Plastic and Reconstructive Surgery, Keck School of Medicine, University of Southern California, Los Angeles, CA, United States;3. Los Angeles County + University of Southern California (LAC+USC) Medical Center, Los Angeles, CA, United States;4. Division of Infectious Diseases, Keck School of Medicine, University of Southern California, Los Angeles, CA, United States;5. Sidney Kimmel Medical College at Thomas Jefferson University, Philadelphia, PA, United States;1. The Welsh Centre for Burns & Plastic Surgery, Morriston Hospital, Swansea SA6 6NL, United Kingdom;2. Department of Trauma & Orthopaedic Surgery, Morriston Hospital, Swansea SA6 6NL, United Kingdom;1. Université de Lille, U1019 – UMR 8204 – CIIL – Center for Infection and Immunity of Lille, F-59000 Lille, France;2. CNRS, UMR 8204, F-59000 Lille, France;3. Inserm, U1019, F-59000 Lille, France;4. CHU Lille, Laboratoire de Parasitologie–Mycologie, F-59000 Lille, France;5. Institut Pasteur de Lille, F-59000 Lille, France;6. Chrono-Environnement UMR 6249 CNRS, Université de Bourgogne Franche–Comté & Laboratoire de Parasitologie–Mycologie, CHU de Besançon, France;7. CHU Lille, Pôle d''Anesthésie-Réanimation, Centre de Traitement des Brûlés, F-59000 Lille, France;8. CHU Lille, Pharmacie Centrale, F-59000 Lille, France;9. CHU Lille, Service de chirurgie plastique, esthétique et reconstructrice – Centre de Traitement des Brûlés, F-59000 Lille, France;10. CHU Lille, Pôle de Réanimation, F-59000 Lille, France;1. Ross Tilley Burn Centre, Sunnybrook Health Sciences Centre, Toronto, Canada;2. Division of Plastic and Reconstructive Surgery, Department of Surgery, University of Toronto, Canada;1. Burn Center, Ghent University Hospital, C. Heymanslaan 10, 9000 Ghent, Belgium;2. Department of Plastic Surgery, Ghent University Hospital, C. Heymanslaan 10, 9000 Ghent, Belgium;3. Department of Plastic and Reconstructive Surgery and Burn Unit, Soroka University Medical Center, Ben-Gurion University of the Negev, Beer-Sheba, Israel
Abstract:IntroductionMucormycosis is an opportunistic fungal infection with a high mortality rate. Though typically associated with diabetes and other conditions that affect innate immune function, infections can also be precipitated by conditions such as trauma and burns. Burn patients are particularly susceptible to fungal infections due to the immune dysfunction that often accompany their wounds. Indeed case series have described mucormycosis to occur in patients with burn injuries, however the factors contributing to mortality have not been well described. Thus, the purpose of our review was to identify factors contributing to morbidity and mortality in burn patients with Mucormycosis.MethodsA systematic review of the literature of mucormycosis infection in burn injury patients was performed on Pubmed and Google Scholar using the keywords: Mucor, Mucorales, Mucormycosis, Mucormycotina, Zygomycosis and burn or thermal injury. Clinical trials, observational studies, case reports, and case reviews were included if they provided information regarding mortality in adult and pediatric burn patients diagnosed with mucormycosis, review articles, non-English articles, and articles without patient information were excluded. No time limit was placed on our review. Individual patient data was stratified based on mortality. Statistical analysis was performed to investigate the relationship between patient risk factors and mortality, and the Oxford Level of Evidence was used to evaluate study quality.Results46 articles were included in our final review, encompassing 114 patients. On average, survivors had a total body surface area (TBSA)% of 46 (SD 19.8) while non-survivors had a TBSA of 65% (SD 16.4), and this difference was significant (p < .001). Patients with disseminated mucormycosis experienced an 80% mortality rate compared to 36% mortality rate in patients with localized disease (p < .001). We found no statistically significant difference in mean age (p > .05), diabetes (p > .05), mean delay in diagnosis (p > .05), time to antifungal therapy (p > .05), or type of therapy used (p > .05) between survivors and non-survivors. Our review was limited by the lack of prospective, controlled trials; thus, our review primarily consists of case reports.ConclusionDisseminated infections and higher TBSA both increased the risk of mortality in burn patients with mucormycosis, while diabetes did not increase mortality risk. The severity of the initial injury and infection locations must be taken into consideration to inform patient prognosis.
Keywords:Mucormycosis  Burn  Mortality  Diabetes  TBSA
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