J Neurol Surg B Skull Base 2023; 84(06): 578-584
DOI: 10.1055/a-1924-9736
Original Article

Postoperative Serum C-Reactive Protein and Cerebrospinal Fluid Leakage after Endoscopic Transsphenoidal Surgery

Rei Yamaguchi
1   Department of Neurosurgery, Gunma University Graduate School of Medicine, Maebashi, Gunma, Japan
,
Masahiko Tosaka
1   Department of Neurosurgery, Gunma University Graduate School of Medicine, Maebashi, Gunma, Japan
,
Naoto Mukada
1   Department of Neurosurgery, Gunma University Graduate School of Medicine, Maebashi, Gunma, Japan
,
Haruka Tsuneoka
1   Department of Neurosurgery, Gunma University Graduate School of Medicine, Maebashi, Gunma, Japan
,
Hiroya Shimauchi-Otaki
1   Department of Neurosurgery, Gunma University Graduate School of Medicine, Maebashi, Gunma, Japan
,
Takaaki Miyagishima
1   Department of Neurosurgery, Gunma University Graduate School of Medicine, Maebashi, Gunma, Japan
,
Fumiaki Honda
1   Department of Neurosurgery, Gunma University Graduate School of Medicine, Maebashi, Gunma, Japan
,
Yuhei Yoshimoto
1   Department of Neurosurgery, Gunma University Graduate School of Medicine, Maebashi, Gunma, Japan
› Institutsangaben
Funding None.

Abstract

Objective Postoperative cerebrospinal fluid (CSF) leakage in endoscopic transsphenoidal surgery is a potential risk that requires immediate repair. We investigated the potential of common postoperative hematological examinations for diagnosing postoperative CSF leakage.

Methods We retrospectively studied 214 consecutive cases who underwent endoscopic transsphenoidal approach (ETSA; transsellar approach) or extended ETSA (E-ETSA). Patients with postoperative CSF leakage were defined the leak group (group L), and patients without were defined as the nonleak group (group N). Postoperative C-reactive protein (CRP) was compared between the ETSA and E-ETSA groups, and between the N and L groups.

Results The values of white blood cell count and CRP 1 to 7 days after surgery were significantly higher in the L group. Especially, CRP was clearly elevated in the L group (p < 0.001). The CRP value was higher in patients in the N group after E-ETSA than after ETSA (p < 0.001). CRP increased on the day after surgery but decreased gradually thereafter in patients after ETSA and in the N group. In contrast, CRP value tended to increase gradually after surgery in the L group. In particular, the CRP on the day before the CSF leak was confirmed was clearly higher than on the fifth to seventh days in the N group.

Conclusion Elevated CRP after endoscopic endonasal transsphenoidal surgery is a potential marker of CSF leakage.



Publikationsverlauf

Eingereicht: 10. April 2022

Angenommen: 03. August 2022

Accepted Manuscript online:
16. August 2022

Artikel online veröffentlicht:
14. September 2022

© 2022. Thieme. All rights reserved.

Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany

 
  • References

  • 1 Ciric I, Ragin A, Baumgartner C, Pierce D. Complications of transsphenoidal surgery: results of a national survey, review of the literature, and personal experience. Neurosurgery 1997; 40 (02) 225-236 , discussion 236–237
  • 2 Sawka AM, Aniszewski JP, Young Jr WF, Nippoldt TB, Yanez P, Ebersold MJ. Tension pneumocranium, a rare complication of transsphenoidal pituitary surgery: Mayo Clinic experience 1976-1998. J Clin Endocrinol Metab 1999; 84 (12) 4731-4734
  • 3 Han ZL, He DS, Mao ZG, Wang HJ. Cerebrospinal fluid rhinorrhea following trans-sphenoidal pituitary macroadenoma surgery: experience from 592 patients. Clin Neurol Neurosurg 2008; 110 (06) 570-579
  • 4 Nishioka H, Haraoka J, Ikeda Y. Risk factors of cerebrospinal fluid rhinorrhea following transsphenoidal surgery. Acta Neurochir (Wien) 2005; 147 (11) 1163-1166 , discussion 1166
  • 5 Black PM, Zervas NT, Candia GL. Incidence and management of complications of transsphenoidal operation for pituitary adenomas. Neurosurgery 1987; 20 (06) 920-924
  • 6 Tabaee A, Anand VK, Brown SM, Lin JW, Schwartz TH. Algorithm for reconstruction after endoscopic pituitary and skull base surgery. Laryngoscope 2007; 117 (07) 1133-1137
  • 7 Borg A, Kirkman MA, Choi D. Endoscopic endonasal anterior skull base surgery: a systematic review of complications during the past 65 years. World Neurosurg 2016; 95: 383-391
  • 8 Oakley GM, Orlandi RR, Woodworth BA, Batra PS, Alt JA. Management of cerebrospinal fluid rhinorrhea: an evidence-based review with recommendations. Int Forum Allergy Rhinol 2016; 6 (01) 17-24
  • 9 Yadav YR, Parihar V, Janakiram N, Pande S, Bajaj J, Namdev H. Endoscopic management of cerebrospinal fluid rhinorrhea. Asian J Neurosurg 2016; 11 (03) 183-193
  • 10 Papadea C, Schlosser RJ. Rapid method for beta2-transferrin in cerebrospinal fluid leakage using an automated immunofixation electrophoresis system. Clin Chem 2005; 51 (02) 464-470
  • 11 Bachmann G, Nekic M, Michel O. Clinical experience with beta-trace protein as a marker for cerebrospinal fluid. Ann Otol Rhinol Laryngol 2000; 109 (12, Pt. 1): 1099-1102
  • 12 Esposito F, Dusick JR, Fatemi N, Kelly DF. Graded repair of cranial base defects and cerebrospinal fluid leaks in transsphenoidal surgery. Oper Neurosurg (Hagerstown) 2007;60(04, Suppl 02)295–303, discussion 303–304
  • 13 Tosaka M, Nagaki T, Honda F, Takahashi K, Yoshimoto Y. Multi-slice computed tomography-assisted endoscopic transsphenoidal surgery for pituitary macroadenoma: a comparison with conventional microscopic transsphenoidal surgery. Neurol Res 2015; 37 (11) 951-958
  • 14 Ahn JY, Kim SH. A new technique for dural suturing with fascia graft for cerebrospinal fluid leakage in transsphenoidal surgery. Neurosurgery 2009;65(6, suppl):65–71, discussion 71–72
  • 15 Tosaka M, Prevedello DM, Yamaguchi R. et al. Single-layer fascia patchwork closure for the extended endoscopic transsphenoidal transtuberculum transplanum approach: deep suturing technique and preliminary results. World Neurosurg 2021; 155: e271-e284
  • 16 Hadad G, Bassagasteguy L, Carrau RL. et al. A novel reconstructive technique after endoscopic expanded endonasal approaches: vascular pedicle nasoseptal flap. Laryngoscope 2006; 116 (10) 1882-1886
  • 17 Kassam AB, Thomas A, Carrau RL. et al. Endoscopic reconstruction of the cranial base using a pedicled nasoseptal flap. Neurosurgery 2008;63(1, suppl 1):ONS44–ONS52, discussion ONS52–ONS53
  • 18 Tosaka M, Shimizu T, Miyagishima T. et al. Combined supra-infrasellar approach to pituitary macroadenoma with oculomotor cistern extension: surgical strategy and experience. Acta Neurochir (Wien) 2019; 161 (05) 1025-1031
  • 19 Huo CW, King J, Goldschlager T. et al. The effects of cerebrospinal fluid (CSF) diversion on post-operative CSF leak following extended endoscopic anterior skull base surgery. J Clin Neurosci 2022; 98: 194-202
  • 20 Ivan ME, Iorgulescu JB, El-Sayed I. et al. Risk factors for postoperative cerebrospinal fluid leak and meningitis after expanded endoscopic endonasal surgery. J Clin Neurosci 2015; 22 (01) 48-54
  • 21 Santotoribio JD, Cuadros-Muñoz JF, García-Casares N. Comparison of C reactive protein and procalcitonin levels in cerebrospinal fluid and serum to differentiate bacterial from viral meningitis. Ann Clin Lab Sci 2018; 48 (04) 506-510
  • 22 Kalchev Y, Petkova T, Raycheva R, Argirova P, Stoycheva M, Murdjeva M. Combined testing of cerebrospinal fluid IL-12 (p40) and serum C-reactive protein as a possible discriminator of acute bacterial neuroinfections. Cytokine 2021; 140: 155423
  • 23 Klinger A, Buchfelder M, Schlaffer SM, Kremenevskaja N, Kleindienst A. Infection surveillance in transsphenoidal pituitary surgery - comparison of lipopolysaccharide-binding-protein, interleukin 6, C-reactive protein, white blood cell count, erythrocyte sedimentation rate and body temperature. Acta Neurochir (Wien) 2013; 155 (11) 2177-2182 , discussion 2182
  • 24 Tuttolomondo A, Di Sciacca R, Di Raimondo D, Renda C, Pinto A, Licata G. Inflammation as a therapeutic target in acute ischemic stroke treatment. Curr Top Med Chem 2009; 9 (14) 1240-1260
  • 25 Tillett WS, Francis T. Serological reactions in pneumonia with a non-protein somatic fraction of pneumococcus. J Exp Med 1930; 52 (04) 561-571
  • 26 Csajbok LZ, Nylén K, Öst M, Sonander H, Nellgård B. In-hospital C-reactive protein predicts outcome after aneurysmal subarachnoid haemorrhage treated by endovascular coiling. Acta Anaesthesiol Scand 2015; 59 (02) 255-264
  • 27 Ballou SP, Kushner I. C-reactive protein and the acute phase response. Adv Intern Med 1992; 37: 313-336
  • 28 Mustard Jr RA, Bohnen JM, Haseeb S, Kasina R. C-reactive protein levels predict postoperative septic complications. Arch Surg 1987; 122 (01) 69-73
  • 29 Orriss DE. Serial serum C-reactive protein levels as an indicator of infection in cardiac transplant patients. Med Lab Sci 1988; 45 (02) 116-120
  • 30 Al-Jabi Y, El-Shawarby A. Value of C-reactive protein after neurosurgery: a prospective study. Br J Neurosurg 2010; 24 (06) 653-659
  • 31 Meyer B, Schaller K, Rohde V, Hassler W. The C-reactive protein for detection of early infections after lumbar microdiscectomy. Acta Neurochir (Wien) 1995; 136 (3-4): 145-150
  • 32 Mirzayan MJ, Gharabaghi A, Samii M, Tatagiba M, Krauss JK, Rosahl SK. Response of C-reactive protein after craniotomy for microsurgery of intracranial tumors. Neurosurgery 2007; 60 (04) 621-625 , discussion 625
  • 33 Choi JJ, Kim HS, Lee KC, Hur H, Jo YY. Prediction of in-hospital mortality and morbidity using high-sensitivity C-reactive protein after burr hole craniostomy. J Anesth 2016; 30 (06) 956-960
  • 34 Hernández Ortiz OH, García García HI, Muñoz Ramírez F. et al. Development of a prediction rule for diagnosing postoperative meningitis: a cross-sectional study. J Neurosurg 2018; 128 (01) 262-271