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Change in regional cerebral blood flow following glycerol administration predicts

Clinical result from shunting in normal pressure hydrocephalus

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Summary

Cerebral haemodynamics were measured in 22 adult patients with secondary normal pressure hydrocephalus (NPH) before and after glycerol administration to determine which patients might benefit from a shunt procedure. Of these 22 patients, 14 were found to be shunt-responsive (group 1) and 8 were shunt-unresponsive (group 2).

Measurement of regional cerebral blood flow (rCBF) was performed by xenon-enhanced computerized tomography (XeCT). Clinical factors such as the Evans' index and the presence or absence of brain atrophy, periventricular lucency (PVL), ventricular reflux, stagnation of cerebrospinal fluid on cisternography, and increased intracranial pressure were not statistically significant predictors of shunt responsiveness. Preoperative rCBF values did not differ between groups 1 and 2.

The rCBF value in every cerebral region of group 1 patients increased significantly after shunting except for the basal ganglia. On preoperative rCBF measurement, all rCBF values in group 1 significantly increased after glycerol administration except for the periventricular lucency (PVL). Patients in group 2, however, lacked such an increase in rCBF.

We therefore propose that, in patients with secondary NPH, shunt surgery will be likely to be effective in those with a demonstrated rise in rCBF after glycerol administration.

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References

  1. Adams RD, Fisher CM, Hakim S, Ojemann RG, Sweet WH (1965) Symptomatic occult hydrocephalus with “nrmal” cerebrospinal fluid pressure. N Engl J Med 273: 117–126

    PubMed  Google Scholar 

  2. Ahlberg J, Norlen L, Blomstrand C, Wikkelso C (1988) Outcome of shunt operation on urinary incontinence in normal pressure hydrocephalus predicted by lumbar puncture. J Neurol Neurosurg Psychiatry 51: 105–108

    PubMed  Google Scholar 

  3. Baron JC, Bousser MG, Rey A, Guilland A, Comar D, Castaigne P (1981) Reversal of focal “misery-perfusion syndrome” by extra-intracranial arterial bypass in hemodynamic cerebral ischemia. A case study with15O positron emission tomography. Stroke 12: 454–459

    PubMed  Google Scholar 

  4. Conner ES, Foley L, Black PM (1984) Experimental normal-pressure hydrocephalus is accompanied by increased transmantle pressure. J Neurosurg 61: 322–327

    PubMed  Google Scholar 

  5. Del Bigio MR, Bruni JE (1988) Changes in periventricular vasculature of rabbit brain following induction of hydrocephalus and after shunting. J Neurosurg 69: 115–120

    PubMed  Google Scholar 

  6. Edwards MSB, Harrison MR, Halks-Miller M, Nakayama Don K, Berger MS, Glick PL, Chinn DH (1984) Koalin-induced congenital hydrocephalus in utero in fetal lambs and rhesus monkeys. J Neurosurg 60: 115–122

    PubMed  Google Scholar 

  7. Fisher CM (1977) The clinical picture in occult hydrocephalus. Clin Neurosurg 24: 270–284

    PubMed  Google Scholar 

  8. Greitz TVB, Grepe AOL, Kalmer MSF, Lopez J (1969) Pre- and postoperative evaluation of cerebral blood flow in low-pressure hydrocephalus. J Neurosurg 31: 644–651

    PubMed  Google Scholar 

  9. Hakim S, Venegas JG, Burton JD (1976) The physics of the cranial cavity, hydrocephalus and normal pressure hydrocephalus: mechanical interpretation and mathematical model. Surg Neurol 5: 187–210

    PubMed  Google Scholar 

  10. Ishikawa M, Kikuchi H, Taki W, Kobayashi A, Nishizawa S, Yonekura Y, Konishi J (1989) Regional cerebral blood flow and oxygen metabolism in normal pressure hydrocephalus after subarachnoid hemorrhage. Neurol Med Chir (Tokyo) 29: 382–388

    Google Scholar 

  11. Ishikawa M, Kikuchi H, Nagata I, Yamagata S, Taki W, Kobayashi A, Yonekura Y, Nishizawa S (1989) The effect of glycerol on regional cerebral blood flow, blood volume and oxygen metabolism. No Shinkei Geka 17: 635–640 (Japanese, Englishabstr)

    PubMed  Google Scholar 

  12. Jack Jr CR, Mokri B, Laws Jr ER, Houser OW, Baker Jr HL, Petersen RC (1987) MR findings in normal pressure hydrocephalus: significance and comparison with other forms of dementia. J Compt Assist Tomogr 11: 923–931

    Google Scholar 

  13. Kashiwagi F, Katayama Y, Suzuki S, Shimizu J, Nagazumi A, Terashi A (1988) Effect of glycerol administration on experimental cerebral ischemia, part 1. Studies on lipid peroxides, prostaglandins, brain edema and brain metabolites. Brain Nerve 40: 179–185 (Japanese, English abstr)

    PubMed  Google Scholar 

  14. Kimura M, Tanaka A, Yoshinaga S (1992) Significance of periventricular hemodynamics in normal pressure hydrocephalus. Neurosurgery 30: 701–705

    PubMed  Google Scholar 

  15. Kushner M, Younkin D, Weinberger J, Hurtig H, Goldberg H, Reivich M (1984) Cerebral hemodynamics in the diagnosis of normal pressure hydrocephalus. Neurology (Cleveland) 34: 96–99

    Google Scholar 

  16. Mamo HL, Meric PC, Ponsin JC, Rey AC, Luft AG, Seylaz JA (1987) Cerebral blood flow in normal pressure hydrocephalus. Stroke 18: 1074–1080

    PubMed  Google Scholar 

  17. Mathew NT, Meyer JS, Hartmann A, Ott EO (1975) Abnormal cerebrospinal fluid-blood flow dynamics, implications in diagnosis, treatment, and prognosis in normal pressure hydrocephalus. Arch Neurol 32: 657–664

    PubMed  Google Scholar 

  18. Meyer JS, Fukuuchi Y, Shimazu K, Ohuchi T, Ericsson AD (1972) Effect of intravenous infusion of glycerol on hemispheric blood flow and metabolism in patients with acute cerebral infarction. Stroke 3: 168–180

    PubMed  Google Scholar 

  19. Meyer JS, Tachibana H, Hardenberg JP, Dowell RE Jr, Kitagawa Y, Mortel K (1984) Normal pressure hydrocephalus, influences on cerebral hemodynamic and cerebrospinal fluid pressure-chemical autoregulation. Surg Neurol 21: 195–203

    PubMed  Google Scholar 

  20. Meyer JS, Kitagawa Y, Tanahashi N, Tachibana H, Kandula P, Cech DA, Clifton GL, Rose JE (1985) Evaluation of treatment of normal-pressure hydrocephalus. J Neurosurg 62: 513–521

    PubMed  Google Scholar 

  21. Muizelaar JP, Wei EP, Kontos HA, Becker DP (1986) Cerebral blood flow is regulated by blood pressure and in blood viscosity alike. Stroke 17: 44–48

    PubMed  Google Scholar 

  22. Oka N, Nakada J, Endo S, Takaku A (1986) Angioarchitecture in experimental hydrocephalus. Pediatr Neurosci 12: 294–299

    Google Scholar 

  23. Oki S, Katoh Y, Kurisu K, Nakahara T, Uozumi T, Tokuda Y, Emoto K, Nishimura S (1989) Effect of glycerol on brain function in normal volunteers, study on regional cerebral blood flow, average topographic EEG and significance probability mapping. In: Hoff JT, Betz AL (eds) Intracranial pressure VII. Springer, Berlin Heidelberg New York Tokyo, pp 911–914

    Google Scholar 

  24. Ott EO, Mathew NT, Meyer JS (1974) Redistribution of regional cerebral blood flow after glycerol infusion in acute cerebral infarction. Neurology 24: 1117–1126

    PubMed  Google Scholar 

  25. Plets C (1986) Influence of experimental hydrocephalus on cerebral vascularization. In: Baethmann A,et al (eds) Mechanisms of secondary brain damage. Plenum, New York, pp 169–178

    Google Scholar 

  26. Sasaki T, Matsuzaki T, Nakagawara J, Satoh S, Kawai Y, Suematsu K (1983) Improvement of CBF by glycerol administration in hypertensive intracerebral hemorrhage. Brain Nerve 35: 505–510 (Japanese, English abstr)

    PubMed  Google Scholar 

  27. Shimoda M, Kawamata F, Yamamoto M, Ohsuga H, Hidaka M, Oda S, Shibuya N, Yamamoto I, Sato O (1989) The evaluation of cerebral hemodynamics in patients with intracranial tumors by stable Xenon CT: the effect of glycerol administration on regional cerebral blood flow. Progress in CT 11: 161–168 (Japanese, English abstr)

    Google Scholar 

  28. Shimoda M, Oda S, Sato O, Kawamata F, Yamamoto M (1993) Discrepancy of xenon concentration between end-tidal and blood collection method in xenon enhanced computerized tomography measurement of cerebral blood flow. Neuroradiology 35: 66–68

    Google Scholar 

  29. Symon L, Dorsh NWC (1975) Use of long-term intracranial pressure measurement to assess hydrocephalic patients prior to shunt surgery. J Neurosurg 42: 258–273

    PubMed  Google Scholar 

  30. Vorstrup S, Christensen J, Gjerris F, Sorensen PS, Thomsen AM, Paulson OB (1987) Cerebral blood flow in patients with normal-pressure hydrocephalus before and after shunting. J Neurosurg 66: 379–387

    PubMed  Google Scholar 

  31. Weiler RO, Wisniewski H (1969) Histological and ultrastructural changes with experimental hydrocephalus in adult rabbits. Brain 92: 819–828

    PubMed  Google Scholar 

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Shimoda, M., Oda, S., Shibata, M. et al. Change in regional cerebral blood flow following glycerol administration predicts. Acta neurochir 129, 171–176 (1994). https://doi.org/10.1007/BF01406498

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