Evaluation of Red Cell Distribution Width (RDW) as an Early Marker of Sepsis in Emergency Patients
Main Article Content
Abstract
Background: Sepsis is a time-sensitive emergency condition in which delayed recognition may lead to organ dysfunction, shock, and death. Red Cell Distribution Width (RDW), a routinely available complete blood count parameter, may provide a low-cost supportive marker for early sepsis assessment, particularly in resource-limited emergency settings. Objective: To evaluate admission RDW as a supportive early marker of sepsis among adult emergency patients with suspected infection and to compare RDW with CRP and procalcitonin. Methods: This prospective cohort study was conducted in the Emergency Department of a tertiary care hospital in Lahore, Pakistan. Adult patients with suspected infection requiring sepsis workup were enrolled and classified into sepsis and non-sepsis infection groups according to Sepsis-3 criteria. Admission RDW, CRP, and procalcitonin were measured, and clinical severity indicators were recorded. Diagnostic accuracy assessment using ROC analysis was planned. Results: Patients with sepsis had higher admission RDW than non-sepsis infection patients, with reported values of 15.9 ± 1.8% and 13.7 ± 1.2%, respectively. CRP was also higher in the sepsis group, 128 ± 46 mg/L versus 54 ± 21 mg/L, and procalcitonin was 4.8 ± 2.6 ng/mL versus 0.9 ± 0.4 ng/mL. The sepsis group also had higher heart rate, lower systolic blood pressure, and higher SOFA score. Conclusion: RDW may serve as a simple, low-cost supportive marker in early sepsis assessment, but it should be interpreted alongside clinical evaluation and other biomarkers. Complete ROC statistics, cut-offs, serial RDW values, and adjusted analyses are required before firm diagnostic accuracy conclusions can be drawn
Article Details
Issue
Section

This work is licensed under a Creative Commons Attribution 4.0 International License.
How to Cite
References
1. Singer M, Deutschman CS, Seymour CW, Shankar-Hari M, Annane D, Bauer M, et al. The Third International Consensus Definitions for Sepsis and Septic Shock (Sepsis-3). JAMA. 2016;315(8):801-10. doi:10.1001/jama.2016.0287.
2. Seymour CW, Liu VX, Iwashyna TJ, Brunkhorst FM, Rea TD, Scherag A, et al. Assessment of Clinical Criteria for Sepsis: For the Third International Consensus Definitions for Sepsis and Septic Shock. JAMA. 2016;315(8):762-74. doi:10.1001/jama.2016.0288.
3. Evans L, Rhodes A, Alhazzani W, Antonelli M, Coopersmith CM, French C, et al. Surviving Sepsis Campaign: International Guidelines for Management of Sepsis and Septic Shock 2021. Intensive Care Med. 2021;47(11):1181-247. doi:10.1007/s00134-021-06506-y.
4. Rudd KE, Johnson SC, Agesa KM, Shackelford KA, Tsoi D, Kievlan DR, et al. Global, Regional, and National Sepsis Incidence and Mortality, 1990–2017: Analysis for the Global Burden of Disease Study. Lancet. 2020;395(10219):200-11. doi:10.1016/S0140-6736(19)32989-7.
5. Reinhart K, Daniels R, Kissoon N, Machado FR, Schachter RD, Finfer S. Recognizing Sepsis as a Global Health Priority: A WHO Resolution. N Engl J Med. 2017;377(5):414-7. doi:10.1056/NEJMp1707170.
6. Pierrakos C, Vincent JL. Sepsis Biomarkers: A Review. Crit Care. 2010;14(1):R15. doi:10.1186/cc8872.
7. Wacker C, Prkno A, Brunkhorst FM, Schlattmann P. Procalcitonin as a Diagnostic Marker for Sepsis: A Systematic Review and Meta-Analysis. Lancet Infect Dis. 2013;13(5):426-35. doi:10.1016/S1473-3099(12)70323-7.
8. Simon L, Gauvin F, Amre DK, Saint-Louis P, Lacroix J. Serum Procalcitonin and C-Reactive Protein Levels as Markers of Bacterial Infection: A Systematic Review and Meta-Analysis. Clin Infect Dis. 2004;39(2):206-17. doi:10.1086/421997.
9. Schuetz P, Wirz Y, Sager R, Christ-Crain M, Stolz D, Tamm M, et al. Effect of Procalcitonin-Guided Antibiotic Treatment on Mortality in Acute Respiratory Infections: A Patient-Level Meta-Analysis. Lancet Infect Dis. 2018;18(1):95-107. doi:10.1016/S1473-3099(17)30592-3.
10. Suberviola B, Castellanos-Ortega A, González-Castro A, García-Astudillo LA, Fernández-Miret B. Prognostic Value of Procalcitonin, C-Reactive Protein and Leukocytes in Septic Shock. Med Intensiva. 2012;36(3):177-84. doi:10.1016/j.medin.2011.09.008.
11. Uffen JW, Oomen P, de Regt M, Oosterheert JJ, Kaasjager K. The Prognostic Value of Red Blood Cell Distribution Width in Patients With Suspected Infection in the Emergency Department. BMC Emerg Med. 2019;19(1):76. doi:10.1186/s12873-019-0293-7.
12. Jo YH, Kim K, Lee JH, Kang C, Kim T, Park HM, et al. Red Cell Distribution Width Is a Prognostic Factor in Severe Sepsis and Septic Shock. Am J Emerg Med. 2013;31(3):545-8. doi:10.1016/j.ajem.2012.10.017.
13. Wang AY, Ma HP, Kao WF, Tsai SH, Chang CK. Red Blood Cell Distribution Width Is Associated With Mortality in Elderly Patients With Sepsis. Am J Emerg Med. 2018;36(6):949-53. doi:10.1016/j.ajem.2017.10.056.
14. Wang TH, Hsu YC. Red Cell Distribution Width as a Prognostic Factor and Its Comparison With Lactate in Patients With Sepsis. Diagnostics. 2021;11(8):1474. doi:10.3390/diagnostics11081474.
15. Zhang L, Yu CH, Guo KP, Huang CZ, Mo LY. Prognostic Role of Red Blood Cell Distribution Width in Patients With Sepsis: A Systematic Review and Meta-Analysis. BMC Immunol. 2020;21(1):40. doi:10.1186/s12865-020-00369-6.
16. Wu H, Gui Y, He M, Zhou J, Yue L, Zhang X. Diagnostic Value of RDW for the Prediction of Mortality in Adult Sepsis Patients: A Systematic Review and Meta-Analysis. Front Immunol. 2022;13:997853. doi:10.3389/fimmu.2022.997853.
17. Dankl D, Rezar R, Mamandipoor B, Zhou Z, Wernly S, Wernly B, et al. Red Cell Distribution Width Is Independently Associated With Mortality in Sepsis. Med Princ Pract. 2022;31(2):187-94. doi:10.1159/000522261.
18. Krishna V, Pillai G, Velickakathu Sukumaran S. Red Cell Distribution Width as a Predictor of Mortality in Patients With Sepsis. Cureus. 2021;13(1):e12912. doi:10.7759/cureus.12912.
19. Jandial A, Kumar S, Bhalla A, Sharma N, Varma N, Varma S. Elevated Red Cell Distribution Width as a Prognostic Marker in Severe Sepsis: A Prospective Observational Study. Indian J Crit Care Med. 2017;21(9):552-62. doi:10.4103/ijccm.IJCCM_208_17.
20. Jain K, Sharma D, Patidar M, Nandedkar S, Pathak A, Purohit M. Red Cell Distribution Width as a Predictor of Mortality in Patients With Clinical Sepsis: Experience From a Single Rural Center in Central India. Clin Pathol. 2022;15:2632010X221075592. doi:10.1177/2632010X221075592.
21. Bibi A, Basharat N, Aamir M, Haroon ZH. Procalcitonin as a Biomarker of Bacterial Infection in Critically Ill Patients Admitted With Suspected Sepsis in Intensive Care Unit of a Tertiary Care Hospital. Pak J Med Sci. 2021;37(7):1999-2003. doi:10.12669/pjms.37.7.4183.
22. Ali W, Shirazi H, Gul S, Halim A, Ain Q, Zaman Q. Comparison of Procalcitonin Versus C-Reactive Protein in the Detection of Neonatal Sepsis. Pak Armed Forces Med J. 2022;72(1):131-5. doi:10.51253/pafmj.v72i1.2478.
23. Bai P, Rais H, Asif R, et al. Role of Inflammatory Markers in Early Diagnosis of Neonatal Sepsis; C-Reactive Protein or Procalcitonin or Red Cell Distribution Width; A Hospital-Based Study. Pak Armed Forces Med J. 2023;73(6):1703-6. doi:10.51253/pafmj.v73i6.9349.
24. Arshad A, Ayaz A, Haroon MA, Jamil B, Hussain E. Predictors of Clinical Outcomes in Patients With Sepsis: A Retrospective Study From a Tertiary Care Hospital in Pakistan. J Pak Med Assoc. 2024;74(4):608-12. doi:10.47391/JPMA.6818.
25. Arshad A, Ayaz A, Haroon MA, Jamil B, Hussain E. Frequency and Cause of Readmissions in Sepsis Patients Presenting to a Tertiary Care Hospital in a Low-Middle Income Country. Crit Care Explor. 2020;2(2):e0080. doi:10.1097/CCE.0000000000000080.