Elevated D-dimer is Associated with Anemia, Immune Dysregulation, and Hepatic–Renal Dysfunction in Acute Burn Patients
Abstract
BACKGROUND: Burn injury induced increased risk of venous thromboembolism (VTE) due to hypercoagulability, immobilization, and endothelial injury. Despite this risk, VTE in burn patients often remains clinically undetected. Although D-dimer is widely used as a VTE marker, its utility in burn patients is inconsistent, particularly in the early post-burn period. Therefore, this study was conducted to evaluate the correlation between D-dimer levels and factors related to VTE, including hematologic, coagulation, immunologic, organ function parameters, and burn characteristics.
METHODS: An analytical observational study was conducted involving adult patients with acute burn injuries enrolled in Dr. Soetomo General Hospital from March to June 2025. Demographic, anthropometric, burn characteristic, and existing comorbid were documented from subjects’ medical records. Blood samples from subjects were collected immediately via venipuncture. D-dimer was analyzed with Enzyme-Linked Fluorescent Assay (ELFA) method, hematology and coagulation profiles were also assessed using hematology analyzer and automated coagulation system, respectively. Meanwhile, hepatic and renal function were analyzed with chemistry analyzers.
RESULTS: Most burn subjects (18 of 20) demonstrated elevated D-dimer levels. Higher D-dimer levels were associated with increased leukocyte counts and upward trend of RDW-CV and RDW-SD. Further analysis among the subjects with elevated D-dimer level showed significant negative correlations were observed between D-dimer levels and anemia-related parameters, including hemoglobin, erythrocyte count, and hematocrit (all p<0.05). Elevated D-dimer was also associated with immune dysregulation, reflected by increased basophil percentages and decreased immunoglobulin (Ig) levels. Additionally, D-dimer levels showed significant positive correlations with aspartate aminotransferase (AST), alanine aminotransferase (ALT), and blood urea nitrogen (BUN), suggesting a link between hypercoagulability and kidney as well as renal dysfunction following burn injury.
CONCLUSION: Leukocyte count, RDW-CV, and RDW-SD are higher in burn patient with elevated D-dimer levels, suggesting that high D-dimer might be correlated with VTE. Elevated D-dimer in burn patients correlates with several VTE risks including anemia, immune dysregulation, and hepatic–renal dysfunction, indicating early coagulation activation and systemic injury following burn injury.
KEYWORDS: burn injury, D-dimer, hypercoagulability, VTE, anemia, immune dysregulation, organ dysregulation
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Sharma R, Ahuja RB. Burn injuries in clinical practice: Principles and management for general physicians. Curr Med Res Pract. 2024; 14(5): 222-7, CrossRef.
Patinggi SK, Bakhtiar Y, Budijitno S, Susilaningsih N, Bahrudin U. Hydrolyzed VCO cream reduces neutrophil number and increases angiogenesis in mid dermal burn wound healing. Indones Biomed J. 2023; 15(3): 240-6, CrossRef.
Bordeanu-Diaconescu EM, Grosu-Bularda A, Frunza A, Grama S, Andrei MC, Neagu TP, et al. Venous thromboembolism in burn patients: A 5-year retrospective study. Medicina. 2024; 60(2): 258, CrossRef.
Spiridonova TG, Zhirkova EA. Etiology and pathogenesis of burn anemia. the role of the blood transfusion in the treatment of patients with burns. Emerg Med Care. 2018; 7(3): 1-7, CrossRef.
Robins EV. Immunosuppression of the burned patient. Crit Care Nurs Clin North Am. 1989; 1(4): 767-74. Erratum in: Crit Care Nurs Clin North Am. 1990; 2(1): preceding xiii, CrossRef.
Lee N, Bae Y, Jang S, Lee DW, Lee SW. Global, regional, and national burden of burn injury by total body surface area (TBSA) involvement from 1990 to 2021, with projections of prevalence to 2050. Healthcare. 2025; 13(16): 2077, CrossRef.
Dini T, Nugraha Y, Revina R, Karina K. Safety and efficacy of mesenchymal stem cells in burn therapy: Systematic review. Mol Cell Biomed Sci. 2022; 6(3): 104-16, CrossRef.
Schulman S, Makatsariya A, Khizroeva J, Bitsadze V, Kapanadze D. The basic principles of pathophysiology of venous thrombosis. Int J Mol Sci. 2024; 25(21): 11447, CrossRef.
Huang S, Ma Q, Liao X, Yin X, Shen T, Liu X, et al. Identification of early coagulation changes associated with survival outcomes post severe burns from multiple perspectives. Sci Rep. 2024; 14(1): 10457, CrossRef.
Ball RL, Keyloun JW, Brummel-Ziedins K, Orfeo T, Palmieri TL, Johnson LS, et al. Burn-induced coagulopathies: A comprehensive review. Shock. 2020; 54(2): 154-67, CrossRef.
Saraswati I, Armalina D, Setiawan RH, Sinna NM, Arummaisya SN. Opuntia cochenillifera cream accelerates incision and burn wound healing in streptozotocin-induced diabetic mice by enhancing fibroblast. Indones Biomed J. 2025; 17(6): 575-84, CrossRef.
Ahuja RB, Bansal P, Pradhan GS, Subberwal M. An analysis of deep vein thrombosis in burn patients (Part 1): Comparison of D-dimer and Doppler ultrasound as screening tools. Burns. 2016; 42(8): 1686-92, CrossRef.
World Health Organization [Internet]. Burns [updated 2023 Oct 13; cited 2025 Oct 18]. Available from: https://www.who.int/.
Barua P, Iqbal MK, Haque M. postburn elevation in fibrin degradation product is related to burn severity. Chattagram Maa-O-Shishu Hosp Med College J. 2020; 19(1): 43-6, CrossRef.
Killeen RB, Kok SJ. D-Dimer Test. In: StatPearls. Treasure Island: StatPearls Publishing; 2025, NLMID.
Li N, Tan J, Feng X, Li M, Qin L, Zhou J. Early coagulation disorder and the predictive value of D-dimer for deep vein thrombosis in major burn patients. Burns. 2025; 51(3): 107398, CrossRef.
Australian and New Zealand Burn Association [Internet]. Emergency Management of Severe Burns (EMSB) [cited 2025 Oct 18]. Available from: https://www.anzba.org/.
Righini M, Robert-Ebadi H, Le Gal G. Age-adjusted and clinical probability adapted d-dimer cutoffs to rule out pulmonary embolism: A narrative review of clinical trials. J Clin Med. 2024; 13(12): 3441, CrossRef.
Priya V, Saikumar C, Banu F. A retrospective study on d-dimer level correlation with CT scan changes in COVID pneumonia in a tertiary care centre ICU. Int J Curr Microbiol App Sci. 2022; 11(05): 220-4, CrossRef.
Sumiyati Y, Bakri S, Arif M. Correlation between inflammation and fibrinolysis in hypertensive centrally obese subjects: A study on c-reactive protein, plasminogen activator inhibitor-1 and thrombin activatable fibrinolysis inhibitor. Indones Biomed J. 2012; 4(3): 151-6, CrossRef.
Zemaitis MR, Guirguis M, Cindass R. Electrical Injuries. Treasure Island: StatPearls Publishing; 2025, NLMID.
Walsh K, Hughes I, Dheansa B. Management of chemical burns. Br J Hosp Med. 2022; 83(3): 1-12, CrossRef.
Cao Q, He X, Chen X, Han X, Yang L. Red blood cell distribution width at admission and the short-term mortality of patients with severe burn injury: a meta-analysis. Eur J Med Res. 2024; 29(1): 589, CrossRef.
Salvagno GL, Sanchis-Gomar F, Picanza A, Lippi G. Red blood cell distribution width: A simple parameter with multiple clinical applications. Crit Rev Clin Lab Sci. 2015; 52(2): 86-105, CrossRef.
Ananthaseshan S, Bojakowski K, Sacharczuk M, Poznanski P, Skiba DS, Prahl Wittberg L, et al. Red blood cell distribution width is associated with increased interactions of blood cells with vascular wall. Sci Rep. 2022; 12(1): 13676, CrossRef.
Begum N, Hasan M, Ahmed T, Kalam MA. An observational study on levels of serum fibrin degradation product (FDP), d-dimer and procalcitonin in burn sepsis. J Bangladesh Coll Phys. 2023; 41(3): 193-7, CrossRef.
Nickel CH, Kellett J, Cooksley T, Lyngholm LE, Chang S, Imfeld S, et al. The diagnoses and outcomes of emergency patients with an elevated d-dimer over the next 90 days. Am J Med. 2021; 134(2): 260-6.e2, CrossRef.
Kowal-Vern A, Walenga JM, Hoppensteadt D, Gamelli RL. Prothrombin fragment 1.2 and modified antithrombin as predictors of disseminated intravascular coagulation and thrombotic risk in thermal injury. J Burn Care Res. 2013; 34(4): 459-64, CrossRef.
Hariani NP, Putra A, Subchan P, Setiawan E. Mesenchymal stem cell-derived exosomes enhance fgf-1 and sdf-1 expression in rats with second degree burns. Mol Cell Biomed Sci. 2025; 9(2): 115-23, CrossRef.
Sobouti B, Fallah S, Ghavami Y, Moradi M. Serum immunoglobulin levels in pediatric burn patients. Burns. 2013; 39(3): 473-6, CrossRef.
Schug W, Loeb S, Dunaway L, Carvalho A, Isakson B. Cardiometabolic disease enhances basophil-endothelium interactions for inflammation resolution. Physiology. 2025; 40(S1): S1.0939, CrossRef.
Yamanishi Y, Miyake K, Iki M, Tsutsui H, Karasuyama H. Recent advances in understanding basophil-mediated Th2 immune responses. Immunol Rev. 2017; 278(1): 237-45, CrossRef.
Dobson GP, Morris JL, Letson HL. Pathophysiology of severe burn injuries: new therapeutic opportunities from a systems perspective. J Burn Care Res. 2024; 45(4): 1041-50, CrossRef.
Guilabert P, Martin N, Usúa G, Vendrell M, Colomina MJ, Barret JP. Coagulation alterations in major burn patients: A narrative review. J Burn Care Res. 2023; 44(2): 280-92, CrossRef.
García-Avello A, Lorente JA, Cesar-Perez J, García-Frade LJ, Alvarado R, Arévalo JM, et al. Degree of hypercoagulability and hyperfibrinolysis is related to organ failure and prognosis after burn trauma. Thromb Res. 1998; 89(2): 59-64, CrossRef.
Niculae A, Gherghina ME, Peride I, Tiglis M, Nechita AM, Checherita IA. Pathway from acute kidney injury to chronic kidney disease: Molecules involved in renal fibrosis. Int J Mol Sci. 2023; 24(18): 14019, CrossRef.
DOI: https://doi.org/10.18585/inabj.v18i1.3925
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