Characteristics of meningitis following transsphenoidal endoscopic surgery: a case series and a systematic literature review
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Abstract
Background
Meningitis occurs in 0.8–1.5% of patients undergoing neurosurgery. The aim of the study was to evaluate the characteristics of meningitis after endoscopic endonasal transsphenoidal surgery (EETS) comparing the findings retrieved to those highlighted by literature search.
Materials and methods
Patients treated by EETS during an 18-year period in the Department of Neurosurgery of ‘Federico II’ University of Naples were evaluated and included in the study if they fulfilled criteria for meningitis. Epidemiological, demographic, laboratory, and microbiological findings were evaluated. A literature research according to PRISMA methodology completed the study.
Results
EETS was performed on 1450 patients, 8 of them (0.6%) had meningitis [median age 46 years (range 33–73)]. Endoscopic surgery was performed 1–15 days (median 4 days) before diagnosis. Meningeal signs were always present. CSF examination revealed elevated cells [median 501 cells/μL (range 30–5728)], high protein [median 445 mg/dL (range 230–1210)], and low glucose [median 10 mg/dL (range 1–39)]. CSF culture revealed Gram-negative bacteria in four cases (Klebsiella pneumoniae, Escherichia coli, Alcaligenes spp., and Haemophilus influenzae), Streptococcus pneumoniae in two cases, Aspergillus fumigatus in one case. An abscess occupying the surgical site was observed in two cases. Six cases reported a favorable outcome; two died. Incidence of meningitis approached to 2%, as assessed by the literature search.
Conclusions
Incidence of meningitis after EETS is low despite endoscope goes through non-sterile structures; microorganisms retrieved are those present within sinus microenvironment. Meningitis must be suspected in patients with persistent fever and impaired conscience status after EETS.
Keywords
Meningitis Transsphenoidal endoscopic surgery Antibiotic treatment Prophylaxis Nosocomial infection NeurosurgeryNotes
Compliance with ethical standards
Conflict of interest
None.
Ethical approval
Internal review board judged the project of the study and the final title of the paper compliant with ethical standards.
Informed consent
Each patient signed an informed consent before surgical procedure and when he was admitted to the Unit of Infectious Diseases.
Funding
No funding was received for this study.
Transparency declarations
None to declare.
Supplementary material
References
- 1.McIntyre PB, O’Brien KL, Greenwood B, van de Beek D. Effect of vaccines on bacterial meningitis worldwide. Lancet. 2012;380:1703–11. doi: 10.1016/S0140-6736(12)61187-8.CrossRefPubMedGoogle Scholar
- 2.Castelblanco RL, Lee M, Hasbun R. Epidemiology of bacterial meningitis in the USA from 1997 to 2010: a population-based observational study. Lancet Infect Dis. 2014;14:813–9. doi: 10.1016/S1473-3099(14)70805-9.CrossRefPubMedGoogle Scholar
- 3.McClelland S 3rd, Hall WA. Postoperative central nervous system infection: incidence and associated factors in 2111 neurosurgical procedures. Clin Infect Dis. 2007;45:55–9. doi: 10.1086/518580.CrossRefPubMedGoogle Scholar
- 4.Pellegrino P, Carnovale C, Perrone V, Salvati D, Gentile M, Brusadelli T, et al. Epidemiological analysis on two decades of hospitalisations for meningitis in the United States. Eur J Clin Microbiol Infect Dis. 2014;33:1519–24. doi: 10.1007/s10096-014-2102-2.CrossRefPubMedGoogle Scholar
- 5.van de Beek D, Drake JM, Tunkel AR. Nosocomial bacterial meningitis. N Engl J Med. 2010;362:146–54. doi: 10.1056/NEJMra0804573.CrossRefPubMedGoogle Scholar
- 6.Chochua S, D’Acremont V, Hanke C, Alfa D, Shak J, Kilowoko M, et al. Increased nasopharyngeal density and concurrent carriage of Streptococcus pneumoniae, Haemophilus influenzae, and Moraxella catarrhalis are associated with pneumonia in febrile children. PLoS One. 2016;11:e0167725. doi: 10.1371/journal.pone.0167725.CrossRefPubMedPubMedCentralGoogle Scholar
- 7.Revai K, Mamidi D, Chonmaitree T. Association of nasopharyngeal bacterial colonization during upper respiratory tract infection and the development of acute otitis media. Clin Infect Dis. 2008;46:e34–7. doi: 10.1086/525856.CrossRefPubMedPubMedCentralGoogle Scholar
- 8.Wolter N, Tempia S, Cohen C, Madhi SA, Venter M, Moyes J, et al. High nasopharyngeal pneumococcal density, increased by viral coinfection, is associated with invasive pneumococcal pneumonia. J Infect Dis. 2014;210:1649–57. doi: 10.1093/infdis/jiu326.CrossRefPubMedGoogle Scholar
- 9.Cappabianca P, Cavallo LM, de Divitiis E. Endoscopic endonasal transsphenoidal surgery. Neurosurgery. 2004;55:933–40.CrossRefPubMedGoogle Scholar
- 10.de Divitiis E, Cappabianca P, Cavallo LM. Endoscopic transsphenoidal approach: adaptability of the procedure to different sellar lesions. Neurosurgery. 2002;51:699–705.CrossRefPubMedGoogle Scholar
- 11.Cappabianca P, Cavallo LM, Esposito F, de Divitiis O, Messina A, de Divitiis E. Extended endoscopic endonasal approach to the midline skull base: the evolving role of transsphenoidal surgery. In: Pickard JD, Akalan N, Di Rocco C, Dolenc VV, Lobo Antunes J, Mooij JJA, Schramm J, Sindou M, editors. Advances and technical standards in neurosurgery. Wien New York: Springer; 2008. p. 152–99.Google Scholar
- 12.Catapano G, de Notaris M, Di Maria D, Fernandez LA, Di Nuzzo G, Seneca V, et al. The use of a three-dimensional endoscope for different skull base tumors: results of a preliminary extended endonasal surgical series. Acta Neurochir. 2016;158:1605–16. doi: 10.1007/s00701-016-2847-8.CrossRefPubMedGoogle Scholar
- 13.Halvorsen H, Ramm-Pettersen J, Josefsen R, Rønning P, Reinlie S, Meling T, et al. Surgical complications after transsphenoidal microscopic and endoscopic surgery for pituitary adenoma: a consecutive series of 506 procedures. Acta Neurochir. 2014;156:441–9. doi: 10.1007/s00701-013-1959-7.CrossRefPubMedGoogle Scholar
- 14.Guvenc G, Kizmazoglu C, Pinar E, Abdülkadir I, Kaya I, Bezircioglu H, et al. Outcomes and complications of endoscopic versus microscopic transsphenoidal surgery in pituitary adenoma. J Craniofac Surg. 2016;27:1015–20. doi: 10.1097/SCS.0000000000002684.CrossRefPubMedGoogle Scholar
- 15.Somma T, Maraolo AE, Esposito F, Cavallo LM, Tosone G, Orlando R, et al. Efficacy of ultra-short single agent regimen antibiotic chemo-prophylaxis in reducing the risk of meningitis in patients undergoing endoscopic endonasal transsphenoidal surgery. Clin Neurol Neurosurg. 2015;139:206–9. doi: 10.1016/j.clineuro.2015.10.007.CrossRefPubMedGoogle Scholar
- 16.Cavallo LM, Messina A, Cappabianca P, Esposito F, de Divitiis E, Gardner P, Tschabitscher M. Endoscopic endonasal surgery of the midline skull base: anatomical study and clinical considerations. Neurosurg Focus. 2005;19:E2.PubMedGoogle Scholar
- 17.Shamseer L, Moher D, Clarke M, Ghersi D, Liberati A, Petticrew M, et al. Preferred reporting items for systematic review and meta-analysis protocols (PRISMA-P) 2015: elaboration and explanation. BMJ. 2015;349:g7647. doi: 10.1136/bmj.i4086.CrossRefGoogle Scholar
- 18.Tian R, Hao S, Hou Z, Gao Z, Liu B. The characteristics of post-neurosurgical bacterial meningitis in elective neurosurgery in 2012: a single institute study. Clin Neurol Neurosurg. 2015;139:41–5. doi: 10.1016/j.clineuro.2015.09.002.CrossRefPubMedGoogle Scholar
- 19.Korinek AM, Baugnon T, Golmard JL, van Effenterre R, Coriat P, Puybasset L. Risk factors for adult nosocomial meningitis after craniotomy: role of antibiotic prophylaxis. Neurosurgery. 2006;59:126–33. doi: 10.1227/01.neu.0000243291.61566.21.CrossRefGoogle Scholar
- 20.Korinek AM, Golmard JL, Elcheick A, Bismuth R, van Effenterre R, Coriat P, Puybasset L. Risk factors for neurosurgical site infections after craniotomy: a critical reappraisal of antibiotic prophylaxis on 4578 patients. Br J Neurosurg. 2005;19:155–62. doi: 10.1080/02688690500145639.CrossRefPubMedGoogle Scholar
- 21.Wang KW, Chang WN, Huang CR, Tsai NW, Tsui HW, Wang HC, Su TM, Rau CS, Cheng BC, Chang CS, Chuang YC, Liliang PC, Tsai YD, Lu CH. Post-neurosurgical nosocomial bacterial meningitis in adults: microbiology, clinical features, and outcomes. J Clin Neurosci. 2005;12:647–50. doi: 10.1016/j.jocn.2004.09.017.CrossRefPubMedGoogle Scholar
- 22.van de Beek D, Cabellos C, Dzupova O, Esposito S, Klein M, Kloek AT, ESCMID, et al. Study Group for Infections of the Brain (ESGIB). ESCMID guideline: diagnosis and treatment of acute bacterial meningitis. Clin Microbiol Infect. 2016;22:S37–62. doi: 10.1016/j.cmi.2016.01.007.CrossRefPubMedGoogle Scholar
- 23.Zarrouk V, Vassor I, Bert F, Bouccara D, Kalamarides M, Bendersky N, et al. Evaluation of the management of postoperative aseptic meningitis. Clin Infect Dis. 2007;44:1555–9.CrossRefPubMedGoogle Scholar
- 24.Somma T, Solari D, Beer-Furlan A, Guida L, Otto B, Prevedello D, et al. Endoscopic endonasal management of rare sellar lesions: clinical and surgical experience on 78 cases and review of the literature. World Neurosurg. 2017;100:369–80. doi: 10.1016/j.wneu.2016.11.057.CrossRefPubMedGoogle Scholar
- 25.Chong MY, Quak SM, Chong CT. Cerebral ischaemia in pituitary disorders—more common than previously thought: two case reports and literature review. Pituitary. 2014;17:171–9. doi: 10.1007/s11102-013-0485-1.CrossRefPubMedGoogle Scholar
- 26.Sylvester PT, Moran CJ, Derdeyn CP, Cross DT, Dacey RG, Zipfel GJ, et al. Endovascular management of internal carotid artery injuries secondary to endonasal surgery: case series and review of the literature. J Neurosurg. 2016;125:1256–76. doi: 10.3171/2015.6.JNS142483.CrossRefPubMedGoogle Scholar
- 27.Takeuchi K, Watanabe T, Nagatani T, Nagata Y, Chu J, Wakabayashi T. Incidence and risk factors of subdural hematoma after intraoperative cerebrospinal fluid leakage during the transsphenoidal approach. Pituitary. 2016;19:565–72. doi: 10.1007/s11102-016-0746-x.CrossRefPubMedGoogle Scholar
- 28.Amano K, Hori T, Kawamata T, Okada Y. Repair and prevention of cerebrospinal fluid leakage in transsphenoidal surgery: a sphenoid sinus mucosa technique. Neurosurg Rev. 2016;39:123–31. doi: 10.1007/s10143-015-0667-6.CrossRefPubMedGoogle Scholar
- 29.Bhatki AM, Pant H, Snyderman CH, Carrau RL, Kassam AB, Prevedello DM, et al. Reconstruction of the cranial base after endonasal skull base surgery: local tissue flaps. Oper Techn Otolaryngol. 2010;21:74–82. doi: 10.1016/j.otot.2009.10.003.CrossRefGoogle Scholar
- 30.Beer R, Pfausler B, Schmutzhard E. Infectious intracranial complications in the neuro-ICU patient population. Curr Opin Crit Care. 2010;16:117–22. doi: 10.1097/MCC.0b013e328338cb5f.PubMedGoogle Scholar
- 31.Ivan ME, Iorgulescu JB, El-Sayed I, McDervott MW, Parsa AT, Pletcher SD, et al. Risk factors for postoperative cerebrospinal fluid leak and meningitis after expanded endoscopic endonasal surgery. J Clin Neurosci. 2015;22:48–54. doi: 10.1016/j.jocn.2014.08.009.CrossRefPubMedGoogle Scholar
- 32.Schenck LP, Surette MG, Bowdish DME. Composition and immunological significance of the upper respiratory tract microbiota. FEBS Lett. 2016;590:3705–20. doi: 10.1002/1873-3468.12455.CrossRefPubMedGoogle Scholar
- 33.Vickery TW, Ramakrishnan VR. Bacterial Pathogens and the Microbiome. Otolaryngol Clin North Am. 2017;50:29–47. doi: 10.1016/j.otc.2016.08.004.CrossRefPubMedGoogle Scholar
- 34.Pagliano P, Ascione T, Boccia G, De Caro F, Esposito S. Listeria monocytogenes meningitis in the elderly: epidemiological, clinical and therapeutic findings. Infez Med. 2016;24:105–11 PMID: 27367319.PubMedGoogle Scholar
- 35.Pagliano P, Attanasio V, Rossi M, Ascione T, Fraganza F, Di Sarno R, et al. Pneumococcal meningitis in cirrhotics: distinctive findings of presentation and outcome. J Infect. 2012;65:577–9. doi: 10.1016/j.jinf.2012.08.019.CrossRefPubMedGoogle Scholar
- 36.Pagliano P, Attanasio V, Rossi M, Carleo MA, Carannante N, Ascione T, et al. Listeria monocytogenes meningitis in the elderly: distinctive characteristics of the clinical and laboratory presentation. J Infect. 2015;71:134–6. doi: 10.1016/j.jinf.2015.02.003.CrossRefPubMedGoogle Scholar