Diagnostic and prognostic utility of c-reactive protein and serum ferritin in children with suspected sepsis: a cross-sectional observational study.
DOI:
https://doi.org/10.51168/ts8rde05Keywords:
Pediatric Sepsis, C-Reactive Protein, Serum Ferritin, Septic Shock, PrognosisAbstract
Introduction Pediatric sepsis requires rapid recognition despite delayed or negative microbiological cultures. C-reactive protein (CRP) and ferritin are accessible inflammatory biomarkers. This study assessed their diagnostic and prognostic associations with culture positivity, septic shock, PRISM III score, and in-hospital mortality. Materials and Methods This prospective observational study included 40 children with suspected sepsis. Clinical details and cultures were recorded, and serum CRP and ferritin were measured at admission and 48 hours. Disease severity was assessed using septic shock status and PRISM III score, with survival recorded. Diagnostic utility for culture positivity was evaluated using sensitivity, specificity, predictive values and ROC analysis, with appropriate statistical tests and p<0.05 considered significant. Results Among 40 children with suspected sepsis, 37.5% were culture-positive. CRP was significantly higher in culture-positive cases at admission (66.93 ± 22.40 vs 51.88 ± 22.68 mg/L; p=0.048) and 48 hours (98.26 ± 15.83 vs 58.55 ± 22.74; p<0.001), with 48-hour AUC of 0.908. Septic shock was associated with higher CRP (71.23 ± 16.90 mg/L) and ferritin (461.70 ± 262.83 ng/mL). Ferritin was markedly higher among non-survivors (657.20 ± 162.73 vs 218.12 ± 225.54 ng/mL; p<0.001). Both CRP (r=0.507) and ferritin (r=0.543) correlated significantly with PRISM III scores. Conclusion CRP, particularly at 48 hours, demonstrated useful diagnostic performance for culture-positive sepsis, while ferritin showed stronger associations with septic shock and mortality. Both biomarkers correlated significantly with PRISM III scores, supporting CRP as a diagnostic marker and ferritin as a useful indicator of severity and prognosis.Recommendations
Serial CRP measurement can complement clinical and microbiological assessment, while ferritin can assist severity and prognostic stratification. Both should be interpreted with culture findings and PRISM III rather than as standalone tests. Larger prospective studies should validate clinically useful cut-offs.
References
1. Weiss SL, Fitzgerald JC, Pappachan J, Wheeler D, Jaramillo-Bustamante JC, Salloo A, et al. Global epidemiology of pediatric severe sepsis: the Sepsis Prevalence, Outcomes, and Therapies study. Am J Respir Crit Care Med. 2015;191(10):1147-57.
https://doi.org/10.1164/rccm.201412-2323OC
2. 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 medicine. 2021 Nov;47(11):1181-247.
3. Cruz AT, Lane RD, Balamuth F, Aronson PL, Ashby DW, Neuman MI, et al. Updates on pediatric sepsis. J Am Coll Emerg Physicians Open. 2020;1(5):981-93.https://doi.org/10.1002/emp2.12173
4. Schlapbach LJ, Watson RS, Sorce LR, Argent AC, Menon K, Hall MW, et al. International consensus criteria for pediatric sepsis and septic shock. JAMA. 2024;331(8):665-74.https://doi.org/10.1001/jama.2024.0179
5. Hilarius KWE, Skippen PW, Kissoon N. Early recognition and emergency treatment of sepsis and septic shock in children. Pediatr Emerg Care. 2020;36(2):101-6.https://doi.org/10.1097/PEC.0000000000002043
6. Scheer CS, Fuchs C, Gründling M, Vollmer M, Bast J, Bohnert JA, et al. Impact of antibiotic administration on blood culture positivity at the beginning of sepsis: a prospective clinical cohort study. Clin Microbiol Infect. 2019;25(3):326-31.
https://doi.org/10.1016/j.cmi.2018.05.016
7. Garcia PCR, Tonial CT, Piva JP. Septic shock in pediatrics: the state-of-the-art. J Pediatr (Rio J). 2020;96 Suppl 1:87-98.
https://doi.org/10.1016/j.jped.2019.10.007
8. Pepys MB, Hirschfield GM. C-reactive protein: a critical update. J Clin Invest. 2003;111(12):1805-12.
https://doi.org/10.1172/JCI200318921
9. Nandy A, Mondal T. Serum ferritin as a diagnostic biomarker for severity of childhood sepsis. Indian Pediatr. 2021;58(12):1143-6.https://doi.org/10.1007/s13312-021-2396-y
10. Garcia PCR, Longhi F, Branco RG, Piva JP, Lacks D, Tasker RC. Ferritin levels in children with severe sepsis and septic shock. Acta Paediatr. 2007;96(12):1829-31.https://doi.org/10.1111/j.1651-2227.2007.00564.x
11. Shaikh GN, Ramamoorthy JG, Parameswaran N, Senthilkumar GP. Serum ferritin for predicting outcome in children with severe sepsis in the pediatric intensive care unit. Indian Pediatr. 2022;59(12):939-42.
https://doi.org/10.1007/s13312-022-2668-1
12. Horvat CM, Fabio A, Nagin DS, Banks RK, Qin Y, Park HJ, et al. Mortality risk in pediatric sepsis based on C-reactive protein and ferritin levels. Pediatr Crit Care Med. 2022;23(12):968-79.https://doi.org/10.1097/PCC.0000000000003074
13. Thapar V, Khinchi Y, Saini SK, Agrawal G, Saini AK, Kumari S. Study of serum ferritin as diagnostic and prognostic biomarker for severity of sepsis: a hospital-based study. Int J Contemp Pediatr. 2024;11(7):945-50.
https://doi.org/10.18203/2349-3291.ijcp20241681
14. Tantray JA, Rashid M, Sohil PR. Study of serum levels of CRP in association with blood culture as an early predictor of sepsis in children: a retrospective study at a tertiary care centre. Int J Med Pharm Res. 2025;6(4):1345-51.
15. Vani KKV, Munagavalasa S, Bhargavi K, Sujatha P, Rani AS. A study on prognostic value of serum ferritin, serum vitamin D and C reactive protein levels in paediatric sepsis. Int J Acad Med Pharm. 2022;4(4):143-9.
16. Tonial CT, Costa CAD, Andrades GRH, Crestani F, Bruno F, Piva JP, et al. Performance of prognostic markers in pediatric sepsis. J Pediatr (Rio J). 2021;97(3):287-94.https://doi.org/10.1016/j.jped.2020.07.008
17. Ghanate DD, Dhotkar S, Bhat P, Patil R. Serum ferritin biomarker as a diagnostic tool in sepsis among PICU patients. Int J Pharm Clin Res. 2023;15(5):2287-91.
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