Pro-calcitonin as a marker of sepsis in NICU setup in comparison to C-reactive protein

Authors

  • Chandrakumar Ramesh Department of Pediatrics, Al Ameen Medical College, Bijapur, Karnataka, India
  • Naushad Ali Malagi Department of Pediatrics, Al Ameen Medical College, Bijapur, Karnataka, India
  • Shivakumar Indi Department of Pediatrics, Al Ameen Medical College, Bijapur, Karnataka, India
  • Nazeer Ahmed Jeergal Department of Pediatrics, Al Ameen Medical College, Bijapur, Karnataka, India
  • Sadashiva B. Ukkali Department of Pediatrics, Al Ameen Medical College, Bijapur, Karnataka, India
  • A. N. Thobbi Department of Pediatrics, Al Ameen Medical College, Bijapur, Karnataka, India

DOI:

https://doi.org/10.18203/2349-3291.ijcp20262950

Keywords:

C-reactive protein, Early onset sepsis, NICU, Negative predictive value, Neonatal sepsis, Procalcitonin, Sensitivity

Abstract

Background: Neonatal sepsis is a major cause of morbidity and mortality, particularly in developing countries. Early diagnosis is difficult because clinical signs are non-specific, blood culture requires 48–72 hours and may have limited sensitivity, while C-reactive protein (CRP) rises relatively late. Procalcitonin (PCT) increases earlier during bacterial infection and may serve as a useful diagnostic marker. This study evaluated PCT as an early marker of neonatal sepsis and compared its diagnostic performance with CRP.

Methods: This prospective cross-sectional study was conducted in the NICU of Al Ameen Medical College, Bijapur, Karnataka, from May 2024 to April 2025. Seventy-five neonates aged less than 72 hours with clinical features or risk factors for sepsis were enrolled. Investigations included complete blood count, absolute neutrophil count, immature-to-total neutrophil ratio, CRP, PCT and blood culture. CRP≥10 mg/l and PCT>0.5 ng/ml were considered positive. Neonates were classified as proven sepsis, suspected sepsis or no sepsis. Data were analysed using Chi-square and Fisher’s exact tests.

Results: Of 75 neonates, 46 (61.3%) were male and 39 (52.0%) had low birth weight. Blood culture was positive in 7 cases (9.3%), with Staphylococcus aureus being the most common isolate. PCT showed higher sensitivity than CRP (85.7% vs 42.8%) and a higher negative predictive value (97.5% vs 93.4%), whereas CRP had greater specificity (83.8% vs 58.8%).

Conclusions: PCT is a more sensitive early marker than CRP for neonatal sepsis. Its high negative predictive value makes it useful for ruling out sepsis and guiding antibiotic decisions.

References

Vergnano S, Sharland M, Kazembe P, Mwansambo C, Heath PT. Neonatal sepsis: an international perspective. Arch Dis Childhood-Fetal Neonatal. 2005;90(3):220-4.

Aggarwal R, Sarkar N, Deorari AK, Paul VK. Sepsis in the newborn. Indian J Pediat. 2001;68(12):1143-7.

Gerdes JS. Diagnosis and management of bacterial infection in the neonate. Pediatric Clin North America. 2004;51(4):939-59.

Stoll BJ. Infections of the neonatal infant. In: Kliegman RM, Stanton BF, Geme JW, editors. Nelson Textbook of Pediatrics. 19th ed. New Delhi: Elsevier. 2012: 629-648.

Benitz WE, Han MY, Madan A, Ramachandra P. Serial serum C-reactive protein levels in the diagnosis of neonatal infections. Pediatrics. 1998;102(4):41.

Mishra UK, Jacobs SE, Doyle LW, Garland SM. Newer approaches to the diagnosis of early onset neonatal sepsis. Arch Dis Childhood-Fetal Neonatal. 2006;91(3):208-12.

Kocabas E, Sarikcioglu A, Aksaray N, Seydaoglu G, Seyhun Y, Yaman A. Role of procalcitonin, C-reactive protein, interleukin-6, interleukin-8 and tumour necrosis factor-alpha in the diagnosis of neonatal sepsis. Turkish J Pedi. 2007;49(1):7-20.

Arkader R, Troster EJ, Lopes MR, Lourenco Junior R, Carcillo JA, Leone C, et al. Procalcitonin does discriminate between sepsis and systemic inflammatory response syndrome. Arch Dis Childhood. 2006;91(2):117-20.

Manroe BL, Weinberg AG, Rosenfeld CR, Browne R. The neonatal blood count in health and disease. I. Reference values for neutrophilic cells. J Pediat. 1979;95(1):89-98.

Lloyd BW, Oto A. Normal values for mature and immature neutrophils in very preterm babies. Arch Dis Childhood. 1982;57(4):233-5.

Tallur SS, Kasturi AV, Nadgir SD, Krishna BVS. Clinico-bacteriological study of neonatal septicaemia in Hubli. Indian J Pediatrics. 2000;67(3):169-74.

Khinchi YR, Kumar A, Yadav S. Profile of neonatal sepsis. J College Medical Sciences-Nepal. 2010;6(1):1-6.

Raghavan M, Mondal GP, Bhatt VR, Srinivasan S. Perinatal risk factors in neonatal infections. Indian Journal of Pediatrics. 1992;59(3):335-40.

Kuruvilla KA, Pillai S, Jesudason M, Jana AK. Bacterial profile of sepsis in a neonatal unit in South India. Indian Pediatrics. 1998;35(9):851-8.

Rodwell RL, Leslie AL, Tudehope DI. Early diagnosis of neonatal sepsis using a hematologic scoring system. J Pediatrics. 1988;112(5):761-7.

Boyle RJ, Chandler BD, Stonestreet BS, Oh W. Early identification of sepsis in infants with respiratory distress. Pediatrics. 1978;62(5):744-750.

Joram N, Boschar C, Denizot S, Doret M, Cambonie G, Flichy-Fernandez AJ. Umbilical cord blood procalcitonin and C-reactive protein concentrations as markers for early diagnosis of very early onset neonatal infection. Archives of Disease in Childhood - Fetal and Neonatal Edition. 2006;91(1):F65-F66.

Bonac B, Derganc M, Wraber B, Hojker S. Interleukin-8 and procalcitonin in early diagnosis of early severe bacterial infection in critically ill neonates. Pflügers Archiv-European J Physiology. 2000;440(1):72-4.

Indino P, Lemarchand P, Bady P, Bonfils P, Gerber S, Morel P, et al. Prospective study on procalcitonin and other systemic markers in patients with leucocytosis. International J Infect Dis. 2008;12(4):319-24.

Janota J, Stranak Z, Belohlavkova S, Mudra K, Simak J. Postnatal increase of procalcitonin in premature newborns is enhanced by chorioamnionitis and neonatal sepsis. European J Clin Invest. 2001;31(11):978-83.

Naher BS, Mannan MA, Noor K, Shahidullah M. Role of serum procalcitonin and C-reactive protein in the diagnosis of neonatal sepsis. Bangladesh Medical Res Council. 2011;37(2):40-6.

Lapillone A, Basson E, Monneret G, Bienvenu J, Salle BL. Lack of specificity of procalcitonin for diagnosis of sepsis in premature infants. Lancet. 1998;351(9110):1211-2.

Koksal N, Harmanci R, Cetinkaya M, Hacimustafaoglu M. The roles of procalcitonin and C-reactive protein in the diagnosis and the follow-up of neonatal sepsis cases. Turkish J Paediat. 2007;49(2):219-24.

Muller B, Schuetz P, Trampuz A. Circulating biomarkers as surrogates for bloodstream infections. Int J Antimicrob Agents. 2007;30(1):16-23.

Ng PC, Cheng SH, Chui KM, Fok TF, Wong MY, Wong W, et al. Diagnosis of late onset sepsis with cytokines, adhesion molecule and C-reactive protein in preterm very low birthweight infants. Archives of Disease in Childhood - Fetal and Neonatal Edition. 1997;77(3):221-7.

Fendler WM, Piotrowski AJ. Procalcitonin in the early diagnosis of nosocomial sepsis in preterm neonates. J Paediat Child Health. 2008;44(3):114-8.

Lachowska M, Gajewska E. Usefulness of procalcitonin (PCT) as a marker of early-onset systemic infections in preterm newborns. Med Sci. 2004;10(2):33-5.

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Published

2026-08-26

How to Cite

Ramesh, C., Malagi, N. A., Indi, S., Jeergal, N. A., Ukkali, S. B., & Thobbi, A. N. (2026). Pro-calcitonin as a marker of sepsis in NICU setup in comparison to C-reactive protein. International Journal of Contemporary Pediatrics, 13(9), 1649–1656. https://doi.org/10.18203/2349-3291.ijcp20262950

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Original Research Articles