Minim Invasive Neurosurg 2007; 50(6): 355-362
DOI: 10.1055/s-2007-993201
Original Article

© Georg Thieme Verlag KG Stuttgart · New York

Improved Outcome in High-Grade Aneurysmal Subarachnoid Hemorrhage by Enhancement of Endogenous Clearance of Cisternal Blood Clots: A Prospective Study that Demonstrates the Role of Lamina Terminalis Fenestration Combined with Modern Microsurgical Cisternal Blood Evacuation

J. Mura 1 , 3 , D. Rojas-Zalazar 1 , 3 , Á. Ruíz 1 , L. C. Vintimilla 1 , 2 , J. J. Marengo 1 , 4
  • 1Institute of Neurosurgery Asenjo, Santiago, Chile
  • 2Regional Hospital of Cuenca, Cuenca, Ecuador
  • 3Department of Neurological Sciences, University of Chile, Santiago, Chile
  • 4Department of Pathophysiology, Institute of Biomedical Sciences, Faculty of Medicine University of Chile, Santiago, Chile
Further Information

Publication History

Publication Date:
22 January 2008 (online)

Abstract

Introduction: Cisternal and ventricular blood predisposes to hydrocephalus and cerebral ischemia after high-grade aneurysmal subarachnoid hemorrhage (HGSAH). We studied the role of lamina terminalis fenestration combined with cisternal blood evacuation in HGSAH.

Patients/Materials and Methods: A clinical, prospective, non-randomized study of a series of HGSAH patients (Modified Fisher ≥3) treated in the acute phase was carried out. The microsurgical treatment included aneurysm clipping, cisternal blood evacuation, and fenestration of the lamina terminalis. A comparable, non-blood-cleansed, endovascular-treated group, was included as a control. Clinical results were evaluated by the Glasgow Outcome Scale (GOS).

Results: During a period of 30 months, 95 patients who met the selection criteria were treated by microsurgical procedures and 28 by endovascular procedures. The distribution of GOS scores was superior for the microsurgical group: good results (GOS 4-5) were obtained in 85.3%, with a mortality rate of 5.9%. By contrast, 60.3% of patients in the endovascular group achieved GOS 4-5 scores, and 15.8% died. Good results for the endovascular group correlated inversely with delay of treatment. A permanent ventriculo-peritoneal shunt was necessary in 3.2% and 7.1% of the microsurgical and endovascular groups, respectively. The incidence of cerebral infarct was 3.1% and 14.3% for the microsurgical and endovascular groups, respectively.

Discussion: Microsurgical management reduces the usually poor outcome of patients with HGSAH. Lamina terminalis fenestration diminishes the incidence of shunt-dependent hydrocephalus and, combined with extensive cisternal blood cleansing, can lower the incidence of stroke. A procedure for cleansing blood and clots from the cisterns in HGSAH, based on the pathophysiology of vasospasm, is proposed.

References

  • 1 Hop J, Rinkel G, Algra A, Gijn J van. Case-fatality rates and functional outcome after subarachnoid hemorrhage: A systematic review.  Stroke. 1997;  28 660-664
  • 2 Rabinstein A, Weigand S, Atkinson JL, Wijdicks EF. Patterns of cerebral infarction in aneurysmal subarachnoid hemorrhage.  Stroke. 2005;  36 992-997
  • 3 Treggiari-Venzi M, Suter P, Romand J. Review of medical prevention of vasospasm after aneurysmal subarachnoid hemorrhage: a problem of neurointensive care.  Neurosurgery. 2001;  48 249-261
  • 4 Dietrich H, Dacey Jr R. Molecular keys to the problems of cerebral vasospasm.  Neurosurgery. 2000;  46 517-530
  • 5 Macdonald R, Weir B. A review of hemoglobin and the pathogenesis of cerebral vasospasm.  Stroke. 1991;  22 971-982
  • 6 Inagawa T, Yamamoto M, Kamiya K. Effect of clot removal on cerebral vasospasms.  J Neurosurg. 1990;  72 224-230
  • 7 Reilly C, Amidei C, Tolentino J, Jahromi BS, Macdonald RL. Clot volume and clearance rate as independent predictors of vasospasm after aneurysmal subarachnoid hemorrhage.  J Neurosurg. 2004;  101 255-261
  • 8 Hijdra A, Gijn J van, Nagelkerke N, Vermeulen M, Crevel H van. Prediction of delayed cerebral ischemia, rebleeding, and outcome after aneurysmal subarachnoid hemorrhage.  Stroke. 1988;  19 1250-1256
  • 9 Charpentier C, Audibert G, Guillemin F, Civit T, Ducrocq X, Bracard S, Hepner H, Picard L, Laxenaire M. Multivariate analysis of predictors of cerebral vasospasm occurrence after aneurysmal subarachnoid hemorrhage.  Stroke. 1999;  30 1402-1408
  • 10 Qureshi A, Sung G, Razumovsky A, Lane K, Straw R, Ulatowski J. Early identification of patients at risk for symptomatic vasospasm after aneurysmal subarachnoid hemorrhage.  Crit Care Med. 2000;  28 984-990
  • 11 Claassen J, Bernardini G, Kreiter K, Bates J, Yunling E, Copeland D, Connolly S, Mayer S. Effect of cisternal and ventricular blood on risk of delayed cerebral ischemia after subarachnoid hemorrhage: The Fisher scale revisited.  Stroke. 2001;  32 2012-2020
  • 12 Frontera J, Claassen J, Schmidt J, Wartenberg K, Temes R, Connolly E, MacDonald R, Mayer S. Prediction of symptomatic vasospasm after subarachnoid hemorrhage: the modified Fisher scale.  Neurosurgery. 2006;  59 21-27
  • 13 Dehdashti A, Rilliet B, Rufenacht D, Tribolet N de. Shunt-dependent hydrocephalus after rupture of intracranial aneurysms: a prospective study of the influence of treatment modality.  J Neurosurg. 2004;  101 402-407
  • 14 Klopfenstein J, Kim L, Feiz-Erfan I, Hott J, Goslar P, Zabramski J, Spetzler R. Comparison of rapid and gradual weaning from external ventricular drainage in patients with aneurysmal subarachnoid hemorrhage: a prospective randomized trial.  J Neurosurg. 2004;  100 225-229
  • 15 Dorai Z, Hynan L, Kopitnik T, Samson D. Factors related to hydrocephalus after aneurysmal subarachnoid hemorrhage.  Neurosurgery. 2003;  52 763-769 , discussion 769-771
  • 16 Graff-Radrod N, Torner J, Adams H, Kassell N. Factors associated with hydrocephalus after subarachnoid hemorrhage: a report of the Cooperative Aneurysm Study.  Arch Neurol. 1989;  46 744-752
  • 17 Kosteljanetz M. CSF dynamics in patients with subarachnoid and/or intraventricular hemorrhage.  J Neurosurg. 1984;  60 940-946
  • 18 Torvik A, Bhatia R, Murthy V. Transitory block of the arachnoid granulations following subarachnoid haemorrhage: a postmortem study.  Acta Neurochir (Wien). 1978;  41 137-146
  • 19 Motohashi O, Suzuki M, Shida N, Umezawa K, Ohtoh T, Sakurai Y, Yoshimoto T. Subarachnoid hemorrhage induced proliferation of leptomeningeal cells and deposition of extracellular matrices in the arachnoid granulations and subarachnoid space. Immunohistochemical study.  Acta Neurochir (Wien). 1995;  136 88-91
  • 20 Sindou M. Favourable influence of opening the lamina terminalis and Lilliequist's membrane on the outcome of ruptured intracranial aneurysms. A study of 197 consecutive cases.  Acta Neurochir (Wien). 1994;  127 15-16
  • 21 Andaluz N, Zuccarello M. Fenestration of the lamina terminalis as a valuable adjunct in aneurysm surgery.  Neurosurgery. 2004;  55 1050-1059
  • 22 Tomasello F, d’Avella D, de Divitiis O. Does Lamina terminalis fenestration reduce the incidence of chronic hydrocephalus after subarachnoid hemorrhage?.  Neurosurgery. 1999;  45 827-832
  • 23 Komotar R, Olivi A, Rigamonti D, Tamargo R. Microsurgical fenestration of the lamina terminalis reduces the incidence of shunt-dependent hydrocephalus after aneurysmal subarachnoid hemorrhage.  Neurosurgery. 2002;  51 1403-1413
  • 24 Varelas P, Helms A, Sinson G, Spanaki M, Hacein-Bey L. Clipping or coiling of ruptured cerebral aneurysms and shunt-dependent hydrocephalus.  Neurocrit Care. 2006;  4 223-228
  • 25 Mizoi K, Yoshimoto T, Takahashi A, Fujiwara S, Koshu K, Sugawara T. Prospective study on the prevention of cerebral vasospasms by intrathecal fibrinolytic therapy with tissue-type plasminogen activator.  J Neurosurg. 1993;  78 430-437
  • 26 Usui M, Saito N, Hoya K, Todo T. Vasospasm prevention with postoperative intrathecal thrombolytic therapy: a retrospective comparison of urokinase, tissue plasminogen activator, and cistemal drainage alone.  Neurosurgery. 1994;  34 235-244
  • 27 Moriyama E, Matsumoto Y, Meguro T, Kawada S, Mandai S, Gohda Y, Sakurai M. Combined cistenal drainage and intrathecal urokinase injection therapy for prevention of vasospasms in patients with aneurysmal subarachnoid hemorrhage.  Neurol Med Chir (Tokyo). 1995;  35 732-736
  • 28 Kasuya H, Shimizy T, Kagawa M. The Effect of continuous drainage of cerebrospinal fluid in patients with subarachnoid hemorrhage: a retrospective analysis of 108 patients.  Neurosurgery. 1991;  28 56-59
  • 29 Hasan D, Tanghe H. Distribution of cysternal blood in patients with acute hydrocephalus after subarachnoid hemorrhage.  Ann Neurol. 1992;  31 374-378
  • 30 Hasan D, Vermeulen M, Wijdicks E, Hijdra A, Gijn J van. Management problems in acute hydrocephalus after subarachnoid hemorrhage.  Stroke. 1989;  6 747-753
  • 31 Hunt W, Hess R. Surgical risk as related to intervention in the repair of intracranial aneurysms.  J Neurosurg. 1968;  28 14-20
  • 32 Suarez J, Tarr R, Selman W. Current concepts in aneurysmal subarachnoid hemorrhage.  N Engl J Med. 2006;  354 387-396
  • 33 Barker  2nd  FG, Ogilvy CS. Efficacy of prophylactic nimodipine for delayed ischemic deficit after subarachnoid hemorrhage: a metaanalysis.  J Neurosurg. 1996;  84 405-414
  • 34 Niskanen M, Koivisto T, Ronkainen A, Rinne J, Ruokonen E. Resource use after subarachnoid hemorrhage: comparison between endovascular and surgical treatment.  Neurosurgery. 2004;  54 1081-1086
  • 35 Koivisto T, Vanninen R, Hurskainen H, Saari T, Hernesniemi JA, Vapalahti M. Outcomes of early endovascular versus surgical treatment of ruptured cerebral aneurysms: A prospective randomized study.  Stroke. 2000;  31 2369-2377
  • 36 Tuffiash E, Tamargo R, Hillis A. Craniotomy for treatment of unruptured aneurysms is not associated with long-term cognitive dysfunction.  Stroke. 2003;  34 2195-2199
  • 37 Frazer D, Ahuja A, Watkins L, Cipolotti L. Coiling versus clipping for the treatment of aneurysmal subarachnoid hemorrhage: a longitudinal investigation into cognitive outcome.  Neurosurgery. 2007;  60 434-442
  • 38 Shiraishi H, Chang CC, Kanno H, Yamamoto I. The relationship between cerebral blood flow and cognitive function in patients with brain insult of various etiology.  J Clin Neurosci. 2004;  11 138-141
  • 39 Molyneux A, Kerr R, Yu L, Clarke M, Sneade M, Yarnold J, Sandercock P. International Subarachnoid Aneurysm Trial (ISAT) Collaborative Group . International Subarachnoid Aneurysm Trial (ISAT) of neurosurgical clipping versus endovascular coiling in 2143 patients with ruptured intracranial aneurysms: a randomized comparison of effects on survival, dependency, seizures, rebleeding, subgroups, and aneurysm occlusion.  Lancet. 2005;  366 809-817
  • 40 Ikeda K, Asakura H, Futami K, Yamashita J. Coagulative and fibrinolytic activation in cerebrospinal fluid and plasma after subarachnoid hemorrhage.  Neurosurgery. 1997;  41 ((2)) 344-349 , discussion 349-350
  • 41 Suzuki M, Kudo A, Otawara Y, Doi M, Kuroda K, Ogawa A. Fibrinolytic activity in the csf and blood following subarachnoid haemorrhage.  Acta Neurochir. 1997;  139 1152-1154
  • 42 Naff N, Williams M, Rigamonti D, Keyl P, Hanley D. Blood Clot resolution in human cerebrospinal fluid: evidence of first-order kinetics.  Neurosurgery. 2001;  49 614-621
  • 43 Andaluz N, Zucarello M. Fenestration of lamina terminalis reduces vasospasm after subarachnoid hemorrhage from anterior communicating artery aneurysms. In: Cerebral Vasospasm Advances in Research and Treatment. Macdonald RL (ed). Thieme Medical Publishers, New York, NY 20045

Correspondence

J. MuraMD 

Institute of Neurosurgery Asenjo

PO Box 3717

Santiago

Chile

Phone: +56/2/575 48 18

Fax: +56/2/575 48 18

Email: jorgemura@terra.cl

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