Skip to main content
Log in

Distinct patterns of postoperative fever in paediatric neurosurgery patients

  • Research
  • Published:
Child's Nervous System Aims and scope Submit manuscript

Abstract

Purpose

Postoperative fever is a common problem following neurosurgery but data on the causes among paediatric patients is sparse. In this report, we determined the incidence, causes, and outcomes of postoperative fever in paediatric neurosurgical patients (< 18 years), and contrasted the findings with an adult cohort published recently from our unit.

Methods

We recruited 61 patients who underwent 73 surgeries for non-traumatic neurosurgical indications over 12 months. A standard protocol was followed for the evaluation and management of postoperative fever. We prospectively collected data pertaining to operative details, daily maximal temperature, clinical features, and use of surgical drains, urinary catheters, and other adjuncts. Elevated body temperature of > 99.9 °F or 37.7 °C for > 48 h or associated with clinical deterioration or localising features was considered as “fever”; elevated temperature not meeting these criteria was classified as transient elevation in temperature (TET).

Results

Twenty-six patients (35.6%) had postoperative fever, more frequent than in adult patients. TET occurred in 12 patients (16.4%). The most common causes of fever were aseptic meningitis (34.6%), followed by urinary tract infections (15.4%), pyogenic meningitis, COVID-19, and wound infections. Postoperative fever was associated with significantly longer duration of hospital admission and was the commonest cause of readmission.

Conclusion

In contrast to adults, early temperature elevations in paediatric patients may portend infectious and serious non-infectious causes of fever, including delayed presentation with aseptic meningitis, a novel association among paediatric patients. Investigation guided by clinical assessment and conservative antibiotic policy in keeping with the institutional microbiological profile provides the most appropriate strategy in managing paediatric postoperative fever.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2

Similar content being viewed by others

Data availability

The datasets generated during and analysed during the current study are available from the corresponding author on reasonable request.

References

  1. Abdelmaseeh TA, Azmat CE, Oliver TI (2021) Postoperative fever. StatPearls

  2. Kinoshita Y, Tominaga A, Saitoh T, Usui S, Takayasu T, Arita K, Sakoguchi T, Sugiyama K, Kurisu K (2013) Postoperative fever specific to neuroendoscopic procedures. Neurosurg Rev. https://doi.org/10.1007/s10143-013-0505-7

    Article  PubMed  Google Scholar 

  3. Raviv N, Field N, Adamo MA (2020) Postoperative fever workup in pediatric neurosurgery patients. J Neurosurg Pediatr 1–5

  4. Wang Z, Shen M, Qiao M, Zhang H, Tang Z (2017) Clinical factors and incidence of prolonged fever in neurosurgical patients. J Clin Nurs 26(3–4):411–417

    Article  PubMed  Google Scholar 

  5. Cunha B (2013) Clinical approach to fever in the neurosurgical intensive care unit: focus on drug fever. Surg Neurol Int 4(6):318

    Article  Google Scholar 

  6. Goyal-Honavar A, Gupta A, Manesh A, Varghese GM, Edmond Jonathan G, Prabhu K, Chacko AG (2022) A prospective evaluation of postoperative fever in adult neurosurgery patients in the COVID-19 era. J Clin Neurosci Off J Neurosurg Soc Australas 103:26–33

    CAS  Google Scholar 

  7. COVIDSurg Collaborative (2020) Delaying surgery for patients with a previous SARS-CoV-2 infection. Br J Surg 107(12):e601–e602

    Article  CAS  Google Scholar 

  8. Gupta A, Goyal-Honavar A, Jonathan GE, Prabhu K, Varghese GM, Rupali P, Chacko AG (2021) Adapting management strategies for sellar-suprasellar lesions during the COVID-19 pandemic: a pragmatic approach from the frontline. Br J Neurosurg 0(0):1–8

    Google Scholar 

  9. Mackowiak PA, Chervenak FA, Grünebaum A (2021) Defining fever. Open Forum. Infect Dis 8(6):ofab161

    Google Scholar 

  10. Mackowiak PA, Wasserman SS, Levine MM (1992) A critical appraisal of 98.6 degrees F, the upper limit of the normal body temperature, and other legacies of Carl Reinhold August Wunderlich. JAMA 268(12):1578–1580

    Article  CAS  PubMed  Google Scholar 

  11. Rudra A, Pal S, Acharjee A (2006) Postoperative fever. Indian J Crit Care Med 10(4):264–271

    Article  Google Scholar 

  12. Rowe TA, Juthani-Mehta M (2014) Diagnosis and management of urinary tract infection in older adults. Infect Dis Clin North Am 28(1):75–89

    Article  PubMed  Google Scholar 

  13. de Kunder SL, ter Laak - Poort MP, Nicolai J, Vles JSH, Cornips EMJ (2016) Fever after intraventricular neuroendoscopic procedures in children. Childs Nerv Syst 32(6):1049–1055

    Article  PubMed  PubMed Central  Google Scholar 

  14. Yousef MAA, Dranginis D, Rosenfeld S (2018) Incidence and diagnostic evaluation of postoperative fever in pediatric patients with neuromuscular disorders. J Pediatr Orthop 38(2):e104–e110

    Article  PubMed  Google Scholar 

  15. Karhade AV, Cote DJ, Larsen AMG, Smith TR (2017) Neurosurgical infection rates and risk factors: a national surgical quality improvement program analysis of 132,000 patients, 2006–2014. World Neurosurg 97:205–212

    Article  PubMed  Google Scholar 

  16. Berg B, Gärdsell P, Skånsberg P (1982) Cerebrospinal fluid lactate in the diagnosis of meningitis. Diagnostic value compared to standard biochemical methods. Scand J Infect Dis 14(2):111–115

    Article  CAS  PubMed  Google Scholar 

  17. Forgacs P, Geyer CA, Freidberg SR (2001) Characterization of chemical meningitis after neurological surgery. Clin Infect Dis 32(2):179–185

    Article  CAS  PubMed  Google Scholar 

  18. Kaufman BA, Tunkel AR, Pryor JC, Dacey RG (1990) Meningitis in the neurosurgical patient. Infect Dis Clin North Am 4(4):677–701

    Article  CAS  PubMed  Google Scholar 

  19. Ross D, Rosegay H, Pons V (1988) Differentiation of aseptic and bacterial meningitis in postoperative neurosurgical patients. J Neurosurg 69(5):669–674

    Article  CAS  PubMed  Google Scholar 

  20. Sanchez GB, Kaylie DM, O’Malley MR, Labadie RF, Jackson CG, Haynes DS (2008) Chemical meningitis following cerebellopontine angle tumor surgery. Otolaryngol-Head Neck Surg Off J Am Acad Otolaryngol-Head Neck Surg 138(3):368–373

    Article  Google Scholar 

  21. Sakushima K, Hayashino Y, Kawaguchi T, Jackson JL, Fukuhara S (2011) Diagnostic accuracy of cerebrospinal fluid lactate for differentiating bacterial meningitis from aseptic meningitis: a meta-analysis. J Infect 62(4):255–262

    Article  PubMed  Google Scholar 

  22. Moorthy RK, Job V, Rebekah G, Rajshekhar V (2022) Cerebrospinal fluid procalcitonin—a potential biomarker for post-craniotomy bacterial meningitis. Neurol India 70(2):721

    Article  PubMed  Google Scholar 

  23. Hussein K, Bitterman R, Shofty B, Paul M, Neuberger A (2017) Management of post-neurosurgical meningitis: narrative review. Clin Microbiol Infect 23(9):621–628

    Article  CAS  PubMed  Google Scholar 

  24. Hillier CE, Stevens AP, Thomas F, Vafidis J, Hatfield R (2000) Aseptic meningitis after posterior fossa surgery treated by pseudomeningocele closure. J Neurol Neurosurg Psychiatry 68(2):218–219

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  25. Jacobs GB, Klemme WM, Murphree HC (1966) Aseptic meningitis and pseudomeningocele formation as a complication of surgery in the posterior fossa. Pac Med Surg 74(6):320–324

    CAS  PubMed  Google Scholar 

  26. Gupta A, Nair RR, Moorthy RK, Rajshekhar V (2018) Effect of staphylococcal decolonization regimen and change in antibiotic prophylaxis regimen on incidence of postcraniotomy aseptic meningitis. World Neurosurg 119:e534–e540

    Article  PubMed  Google Scholar 

  27. Murray CJL, Ikuta KS, Sharara F et al (2022) Global burden of bacterial antimicrobial resistance in 2019: a systematic analysis. Lancet 399(10325):629–655. https://doi.org/10.1016/S0140-6736(21)02724-0

    Article  CAS  Google Scholar 

  28. Boeckel TPV, Gandra S, Ashok A, Caudron Q, Grenfell BT, Levin SA, Laxminarayan R (2014) Global antibiotic consumption 2000 to 2010: an analysis of national pharmaceutical sales data. Lancet Infect Dis 14(8):742–750

    Article  PubMed  Google Scholar 

  29. Laxminarayan R, Duse A, Wattal C et al (2013) Antibiotic resistance-the need for global solutions. Lancet Infect Dis 13(12):1057–1098

    Article  PubMed  Google Scholar 

  30. Bio LL, Schwenk HT, Chen SF, Conlon S, Gallo A, Bonham CA, Gans HA (2021) Standardization of post-operative antimicrobials reduced exposure while maintaining good outcomes in pediatric liver transplant recipients. Transpl Infect Dis Off J Transplant Soc 23(3):e13538

    Article  CAS  Google Scholar 

  31. Moorthy RK, Sarkar H, Rajshekhar V (2013) Conservative antibiotic policy in patients undergoing non-trauma cranial surgery does not result in higher rates of postoperative meningitis: an audit of nine years of narrow-spectrum prophylaxis. Br J Neurosurg 27(4):497–502

    Article  CAS  PubMed  Google Scholar 

  32. Tunkel AR, Hasbun R, Bhimraj A, Byers K, Kaplan SL, Scheld WM, Van De Beek D, Bleck TP, Garton HJL, Zunt JR (2017) 2017 Infectious diseases society of America’s clinical practice guidelines for healthcare-associated ventriculitis and meningitis*. Clin Infect Dis 64(6):e34–e65

    Article  CAS  PubMed  PubMed Central  Google Scholar 

Download references

Funding

 No funding was received to assist with the preparation of this manuscript.

Author information

Authors and Affiliations

Authors

Contributions

AGH, APM, AG, AM, GMV, WR, GEJ, AGC, and KP conceived the protocol and design of the study. AGH and APM wrote the main manuscript text. AG, AM, GMV, WR, GEJ, AGC, and KP critically reviewed the manuscript. All authors reviewed the manuscript. 

Corresponding author

Correspondence to Krishna Prabhu.

Ethics declarations

Ethical approval

The study was approved by the Institutional Review Board (IRB Min. No. 12914 dated 24.06.2020). Written informed consent was obtained from the patient guardians as all patients were aged under 18 years of age.

Conflict of interest

The authors declare no conflict of interest.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Goyal-Honavar, A., Markose, A.P., Gupta, A. et al. Distinct patterns of postoperative fever in paediatric neurosurgery patients. Childs Nerv Syst (2024). https://doi.org/10.1007/s00381-024-06355-2

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1007/s00381-024-06355-2

Keywords

Navigation