Antibiotic resistance in bacterial infections of burn wounds: Challenges, mortality, and solutions
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Abstract
Burn wounds pose a significant clinical challenge due to their vulnerability to bacterial infections, compounded by the frequent emergence of multidrug-resistant (MDR) and extensively drug-resistant (XDR) pathogens. Factors such as immune dysregulation from burn injury, loss of the skin barrier, prolonged hospitalization, and invasive procedures contribute to increased susceptibility to colonization and infection by resistant bacteria, notably Pseudomonas aeruginosa, Acinetobacter baumannii, Klebsiella pneumoniae, and methicillin-resistant Staphylococcus aureus (MRSA). This review synthesizes current evidence on the microbiological landscape of burn wound infections, highlighting high rates of MDR/XDR isolates harboring diverse resistance mechanisms, including carbapenemases and extended-spectrum beta-lactamases. These resistant pathogens significantly impair healing by prolonging inflammation and biofilm formation and severely restrict effective antibiotic options, often necessitating last-resort therapies with associated toxicity. Risk factors predictive of MDR infections include extensive burns, invasive device use, prior antibiotic exposure, and longer intensive care unit (ICU) stays. Clinical management challenges extend from infection control and wound care to antimicrobial stewardship and the integration of emerging diagnostics. Future perspectives emphasize rapid molecular diagnostics, development of novel antimicrobials and topical agents, and multidisciplinary approaches involving surgeons, infectious disease specialists, and pharmacists to optimize outcomes. Prevention strategies targeting both hospital and community settings are critical for reducing burn incidence and infection rates. In conclusion, addressing antibiotic resistance in burn wounds requires comprehensive, evidence-based interventions and continued innovation to reduce morbidity and mortality and lower healthcare costs.
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[1] Elsheikh R, Makram AM. Multidrug-Resistant Organisms: The Silent Plight of Burn Patients. J Burn Care Res. 2024;45(4):877-886. DOI: 10.1093/jbcr/irae075 PMID: 38695094
[2] Golshekan M, Hosseini SA, Aghajan A, Sedigh Ebrahim-Saraie H. Innovative hybrid platforms for overcoming antimicrobial resistance in wound healing: The synergy of mesoporous nanostructures and antimicrobial peptides. Iran J Burns Wound Res. 2025;1(2):52-53. DOI: 10.61882/ijbwr.1.2.15
[3] Nikokar I, Tishayar A, Flakiyan Z, Alijani K, Rehana-Banisaeed S, et al. Antibiotic resistance and frequency of class 1 integrons among Pseudomonas aeruginosa, isolated from burn patients in Guilan, Iran. Iran J Microbiol. 2013;5(1):36-41. PMID: 23466812
[4] Lachiewicz AM, Hauck CG, Weber DJ, Cairns BA, van Duin D. Bacterial Infections After Burn Injuries: Impact of Multidrug Resistance. Clin Infect Dis. 2017;65(12):2130-2136.
DOI: 10.1093/cid/cix682 PMID: 29194526
[5] Mondol SM, Islam MR, Mia ME, Hassan MH, Farhad F, et al. Molecular and genomic insights into multidrug-resistant (MDR) and extensively drug-resistant (XDR) Pseudomonas aeruginosa causing burn wound infections in Bangladesh. Sci Rep. 2025;15(1):32629.
DOI: 10.1038/s41598-025-19576-5 PMID: 40659765
[6] Cui Z, Li Y, Qin Y, Li J, Shi L, et al. Polymyxin B-targeted liposomal photosensitizer cures MDR A. baumannii burn infections and accelerates wound healing via M1/M2 macrophage polarization. J Control Release. 2024;366:297-311.
DOI: 10.1016/j.jconrel.2023.12.046 PMID: 38161034
[7] Pallett SJC, Morkowska A, Woolley SD, Potochilova VV, Rudnieva KL, et al. Evolving antimicrobial resistance of extensively drug-resistant Gram-negative severe infections associated with conflict wounds in Ukraine: an observational study. Lancet Reg Health Eur. 2025;52:101274.
DOI: 10.1016/j.lanepe.2025.101274 PMID: 40224375
[8] Radzikowska-Büchner E, Łopuszyńska I, Flieger W, Tobiasz M, Maciejewski R, et al. An Overview of Recent Developments in the Management of Burn Injuries. Int J Mol Sci. 2023;24(22):16357.
DOI: 10.3390/ijms242216357 PMID: 38003548
[9] Sabzghabaee AM, Abedi D, Fazeli H, Javadi A, Jalali M, et al. Antimicrobial resistance pattern of bacterial isolates from burn wounds in an Iranian University Hospital. J Res Pharm Pract. 2012;1(1):30-3.
DOI: 10.4103/2279-042X.99675 PMID: 24991585
[10] Afshar Yavari S, Farajzadeh F, Diba K, Kazemzadeh J. Frequency and Antibiotic Resistance Patterns of Isolated Bacteria from Burn Wounds Infections in Imam Khomeini Medical Center in Urmia. J Res Appl Basic Med Sci. 2024;10(1):13-22.
URL: http://ijrabms.umsu.ac.ir/article-1-175-en.html
[11] Haghighifar E, Kamali Dolatabadi R. Bacterial infections and antimicrobial resistance patterns of burn wound infections: A one year study from burn Hospital, Isfahan, Iran. J Adv Med Biomed Res. 2020;28(128):144-50. DOI: 10.30699/jambs.28.128.144
[12] Goh M, Du M, Peng WR, Saw PE, Chen Z. Advancing burn wound treatment: exploring hydrogel as a transdermal drug delivery system. Drug Deliv. 2024;31(1):2300945.
DOI: 10.1080/10717544.2023.2300945 PMID: 38366562
[13] Atiyeh B, El Hachem TF, Chalhoub R, Emsieh SE. Have the recent advancements in wound repair and scar management technology improved the quality of life in burn patients? Burns. 2025;51(4):107443.
DOI: 10.1016/j.burns.2025.107443 PMID: 40112656
[14] Żwierełło W, Piorun K, Skórka-Majewicz M, Maruszewska A, Antoniewski J, et al. Burns: Classification, Pathophysiology, and Treatment: A Review. Int J Mol Sci. 2023;24(4):3749.
DOI: 10.3390/ijms24043749 PMID: 36835171
[15] Warby R, Maani CV. Burn Classification. In: StatPearls [Internet]. 2025.
URL: https://www.ncbi.nlm.nih.gov/sites/books/NBK539773/
[16] Vo V, Haidari H, Cowin AJ, Wagstaff M, Dearman B, et al. Dermal Substitutes for Clinical Management of Severe Burn Injuries: Current and Future Perspectives. Adv Ther. 2025;8(3):2400455. DOI: 10.1002/adtp.202400455
[17] Osuna JAB, Chavez VG, Castaneda JAG. Surgical management of burn injuries: current concepts and advancements in reconstructive strategies. Int Surg J. 2025;12(6):1044–1048.
DOI: 10.18203/2349-2902.isj20251550
[18] Neelon J, Thompson MA, Garcia SA, Hicken A, Leatherman L, et al. Development of an experimental heterogeneous burn wound model. Burns. 2025;51(1):107303.
DOI: 10.1016/j.burns.2024.107303 PMID: 39579581
[19] Rangaiah PKB, Kumar BPP, Huss F, Augustine R. Precision diagnosis of burn injuries using imaging and predictive modeling for clinical applications. Sci Rep. 2025;15(1):7604.
DOI: 10.1038/s41598-025-92096-4 PMID: 40038450
[20] Khan A, Mostafa HM, Almohammed KH, Singla N, Bhatti Z, et al. Advances in Nanotechnology in Drug Delivery Systems for Burn Wound Healing: A Review. Biomed Pharmacol J. 2025;18(1):373-86. DOI: 10.13005/bpj/3094
[21] Varshochi M, Hasani A, Pour Shahverdi P, Ravanbakhsh Ghavghani F, Matin S. Risk Factors for the Antibiotic Resistant Gram-Negative Bacilli Associated Infections in Burn Patients and the In-Vitro Susceptibility of Colistin. Arch Clin Infect Dis. 2020;15(3):e91174. DOI: 10.5812/archcid.91174
[22] Mirzaei B, Bazgir ZN, Goli HR, Iranpour F, Mohammadi F, et al. Prevalence of multi-drug resistant (MDR) and extensively drug-resistant (XDR) phenotypes of Pseudomonas aeruginosa and Acinetobacter baumannii isolated in clinical samples from Northeast of Iran. BMC Res Notes. 2020;13(1):380.
DOI: 10.1186/s13104-020-05224-w PMID: 32778154
[23] Singh B, Mehta S, Asare-Amoah J, Appiah PO, Chauhan S, et al. Biofilm-associated Multidrug Resistant Bacteria Among Burn Wound Infections: A Cross-sectional Study. Mediterr J Infect Microb Antimicrob. 2024;13(1):15-15.
DOI: 10.4274/mjima.galenos.2024.24179.15
[24] Shali AAK, Jalal PJ, Arif SK. Dissemination and Genetic Relatedness of Multidrug-Resistant and Extensively Drug-Resistant Acinetobacter baumannii Isolates from a Burn Hospital in Iraq. Can J Infect Dis Med Microbiol. 2022;2022:8243192. DOI: 10.1155/2022/8243192 PMID: 35669527
[25] Sadeq ZE, Lafta IJ. Tigecycline is the most effective against multi-drug resistant Klebsiella pneumoniae recovered from burn wound infections in two hospitals in Al-Kut city, Iraq. Iraqi J Sci. 2024;65(2):659-74. DOI: 10.24996/ijs.2024.65.2.7
[26] Nasser S, Alnasser Z, Aljuhani O, Alharbi A, Rice J, et al. Exploring infection risk factors and multi-drug-resistant organisms (MDROs) in burn intensive care units: a multi-centre case-control study. J Hosp Infect. 2025;162:186-196.
DOI: 10.1016/j.jhin.2025.05.010 PMID: 40456489
[27] Bourgi J, Said JM, Yaakoub C, Atallah B, Al Akkary N, et al. Bacterial infection profile and predictors among patients admitted to a burn care center: A retrospective study. Burns. 2020;46(8):1968-1976.
DOI: 10.1016/j.burns.2020.05.004 PMID: 32522390
[28] Gong Y, Peng Y, Luo X, Zhang C, Shi Y, et al. Different Infection Profiles and Antimicrobial Resistance Patterns Between Burn ICU and Common Wards. Front Cell Infect Microbiol. 2021;11:681731.
DOI: 10.3389/fcimb.2021.681731 PMID: 34277469
[29] Vinaik R, Barayan D, Shahrokhi S, Jeschke MG. Management and prevention of drug resistant infections in burn patients. Expert Rev Anti Infect Ther. 2019;17(8):607-619.
DOI: 10.1080/14787210.2019.1648208 PMID: 31353976
[30] Rowan MP, Cancio LC, Elster EA, Burmeister DM, Rose LF, et al. Burn wound healing and treatment: review and advancements. Crit Care. 2015;19:243.
DOI: 10.1186/s13054-015-0961-2 PMID: 26067660
[31] Greenhalgh DG, Kiley JL. Diagnosis and Treatment of Infections in the Burn Patient. Eur Burn J. 2024;5(3):296-308.
DOI: 10.3390/ebj5030028 PMID: 39599952
[32] Zhou S, Zhang M, Xue L, Li J, Ma X, et al. Dopamine-alginate-zinc ion dressings employing synergistic active and passive antimicrobial strategies for enhanced burn wound infection management and accelerated healing. Carbohydr Polym. 2025;359:123571.
DOI: 10.1016/j.carbpol.2025.123571 PMID: 40306778
[33] Orbay H, Ziembicki JA, Yassin M, Egro FM. Prevention and Management of Wound Infections in Burn Patients. Clin Plast Surg. 2024;51(2):255-265.
DOI: 10.1016/j.cps.2023.11.003 PMID: 38429048