Skip to main content
Top
Published in: Child's Nervous System 7/2012

01-07-2012 | Original Paper

Surgical revascularisation for childhood moyamoya

Authors: J. Ng, D. Thompson, J. P. S. Lumley, D. E. Saunders, V. Ganesan

Published in: Child's Nervous System | Issue 7/2012

Login to get access

Abstract

Purpose

Children with moyamoya disease/syndrome (MM) have a high rate of recurrent arterial ischaemic stroke (AIS) and associated neurological morbidity; surgical revascularisation (SR) has the potential to prevent this. Here we describe our experience of SR for childhood mm.

Methods

This study is a retrospective review of case notes and radiology of children with moyamoya who underwent SR at our centre.

Results

Seventy-three children with MM and who had SR were identified, with median age at presentation of 4.75 years (range 0.6–14.5). Children with >1 AIS or transient ischaemic attack (TIA) and who had not infarcted the whole territory of the diseased carotid artery were offered SR, with the primary aim of preventing further AIS. One hundred and thirty-four SR procedures were undertaken: 82 indirect (62.4 %) and 49 (37.6 %) direct procedures with 3 second SR procedures following initial SR. Median age at surgery was 7.3 (1–18.2) years. There was no perioperative mortality. One anticoagulated child developed an intracranial haemorrhage on the fifth post-operative day. Median duration of follow-up was 34 (5–166) months. Three children (4.1 %) had recurrent AIS (one silent) after SR; two with sickle cell disease had intracranial haemorrhage 1.5 and 11 months post-SR. TIAs improved in 42 out of 53 (79.2 %).

Conclusion

Our experience of SR for paediatric MM is comparable to other large series. SR is safe, and the rate of recurrent AIS after SR is lower than would be anticipated, on the basis of known natural history of MM. There was no observed difference in outcome of recurrent AIS for direct versus indirect procedures in this series.
Literature
1.
go back to reference Fukui M (1997) Guidelines for the diagnosis and treatment of spontaneous occlusion of the circle of Willis (Moyamoya disease) of the Ministry of Health and Welfare, Japan. Clin Neurol Neurosurg 99:S238PubMedCrossRef Fukui M (1997) Guidelines for the diagnosis and treatment of spontaneous occlusion of the circle of Willis (Moyamoya disease) of the Ministry of Health and Welfare, Japan. Clin Neurol Neurosurg 99:S238PubMedCrossRef
2.
go back to reference Nanba R, Kuroda S, Tada M et al (2006) Clinical features of familial moyamoya disease. Childs Nerv Syst 22:258–262PubMedCrossRef Nanba R, Kuroda S, Tada M et al (2006) Clinical features of familial moyamoya disease. Childs Nerv Syst 22:258–262PubMedCrossRef
3.
go back to reference Wakai K, Tamakoshi A, Ikezaki K et al (1997) Epidemiological features of moyamoya disease in Japan: findings of a nationwide survey. Clin Neurol Neurosurg 99:S1–S5PubMedCrossRef Wakai K, Tamakoshi A, Ikezaki K et al (1997) Epidemiological features of moyamoya disease in Japan: findings of a nationwide survey. Clin Neurol Neurosurg 99:S1–S5PubMedCrossRef
4.
go back to reference Kurokawa T, Tomita S, Ueda K et al (1985) Prognosis of occlusive disease of the circle of Willis (moyamoya disease) in children. Padiatr Neurol 1:274–277CrossRef Kurokawa T, Tomita S, Ueda K et al (1985) Prognosis of occlusive disease of the circle of Willis (moyamoya disease) in children. Padiatr Neurol 1:274–277CrossRef
5.
go back to reference Cramer SC, Robertson RL, Dooling EC et al (1996) Moyamoya and Down syndrome. Clinical and radiological features. Stroke 27:2131–2135PubMedCrossRef Cramer SC, Robertson RL, Dooling EC et al (1996) Moyamoya and Down syndrome. Clinical and radiological features. Stroke 27:2131–2135PubMedCrossRef
6.
go back to reference Kuroda S, Hashisumoto N, Yoshimoto T et al (2007) Radiological findings, clinical course and outcome in asymptomatic moyamoya disease: results of multicenter survey in Japan. Stroke 38:1430–1435PubMedCrossRef Kuroda S, Hashisumoto N, Yoshimoto T et al (2007) Radiological findings, clinical course and outcome in asymptomatic moyamoya disease: results of multicenter survey in Japan. Stroke 38:1430–1435PubMedCrossRef
7.
go back to reference Ikeda K, Iwasaki Y, Kashihara H et al (2006) Adult moyamoya disease in the asymptomatic Japanese population. J Clin Neurosci 13:334–338PubMedCrossRef Ikeda K, Iwasaki Y, Kashihara H et al (2006) Adult moyamoya disease in the asymptomatic Japanese population. J Clin Neurosci 13:334–338PubMedCrossRef
8.
go back to reference Ganesan V, Prengler M, Wade A, Kirkham FJ (2006) Clinical and radiological recurrence after childhood arterial ischemic stroke. Circulation 114:2170–2177PubMedCrossRef Ganesan V, Prengler M, Wade A, Kirkham FJ (2006) Clinical and radiological recurrence after childhood arterial ischemic stroke. Circulation 114:2170–2177PubMedCrossRef
9.
go back to reference Fullerton HJ, Wu YW, Sidney S, Johnstone SC (2007) Risk of recurrent childhood arterial ischemic stroke in a population-based cohort: the importance of cerebrovascular imaging. Pediatrics 119:495–501PubMedCrossRef Fullerton HJ, Wu YW, Sidney S, Johnstone SC (2007) Risk of recurrent childhood arterial ischemic stroke in a population-based cohort: the importance of cerebrovascular imaging. Pediatrics 119:495–501PubMedCrossRef
10.
go back to reference Dobson SR, Holden KR, Nietert PJ et al (2002) Moyamoya syndrome in childhood sickle cell disease: a predictive factor for recurrent cerebrovascular events. Blood 99:3144–3150PubMedCrossRef Dobson SR, Holden KR, Nietert PJ et al (2002) Moyamoya syndrome in childhood sickle cell disease: a predictive factor for recurrent cerebrovascular events. Blood 99:3144–3150PubMedCrossRef
11.
go back to reference Fung LW, Thompson D, Ganesan V (2005) Revascularisation surgery for paediatric moyamoya: a review of the literature. Childs Nerv Syst 21:358–364PubMedCrossRef Fung LW, Thompson D, Ganesan V (2005) Revascularisation surgery for paediatric moyamoya: a review of the literature. Childs Nerv Syst 21:358–364PubMedCrossRef
12.
go back to reference Matsushima T, Inoue T, Suzuki SO et al (1992) Surgical treatment of moyamoya disease in pediatric patients—comparison between the results of indirect and direct revascularization procedures. Neurosurgery 31:401–405PubMedCrossRef Matsushima T, Inoue T, Suzuki SO et al (1992) Surgical treatment of moyamoya disease in pediatric patients—comparison between the results of indirect and direct revascularization procedures. Neurosurgery 31:401–405PubMedCrossRef
13.
go back to reference Scott RM, Smith RL, Robertson RL et al (2004) Long-term outcome in children with moyamoya syndrome after cranial revascularisation by pial synangiosis. J Neurosurg 100(2 Suppl Pediatrics):142–149PubMed Scott RM, Smith RL, Robertson RL et al (2004) Long-term outcome in children with moyamoya syndrome after cranial revascularisation by pial synangiosis. J Neurosurg 100(2 Suppl Pediatrics):142–149PubMed
14.
go back to reference Chui D, Shedden P, Bratina P et al (1998) Clinical features of moyamoya disease in the United States. Stroke 29:1347–1351CrossRef Chui D, Shedden P, Bratina P et al (1998) Clinical features of moyamoya disease in the United States. Stroke 29:1347–1351CrossRef
15.
go back to reference Uchino K, Claiborne J, Becker KJ et al (2005) Moyamoya in Washington State and California. Neurology 65:956–958PubMedCrossRef Uchino K, Claiborne J, Becker KJ et al (2005) Moyamoya in Washington State and California. Neurology 65:956–958PubMedCrossRef
16.
go back to reference Lee M, Zaharchuk G, Guzman R et al (2009) Quantitative hemodynamic studies in moyamoya disease. Neurosurg Focus 26(4):E5PubMedCrossRef Lee M, Zaharchuk G, Guzman R et al (2009) Quantitative hemodynamic studies in moyamoya disease. Neurosurg Focus 26(4):E5PubMedCrossRef
17.
go back to reference Sakamoto H, Kitano S, Yasui T et al (1997) Direct extracranial–intracranial bypass for children with moyamoya disease. Clin Neurol Neurosurg 99:S126–S131CrossRef Sakamoto H, Kitano S, Yasui T et al (1997) Direct extracranial–intracranial bypass for children with moyamoya disease. Clin Neurol Neurosurg 99:S126–S131CrossRef
18.
go back to reference Iwama T, Hashimoto N, Yonekawa Y (1996) The relevance of hemodynamic factors to perioperative ischemic complications in childhood moyamoya disease. Neurosurgery 38:1120–1125, discussion 1125–1126PubMed Iwama T, Hashimoto N, Yonekawa Y (1996) The relevance of hemodynamic factors to perioperative ischemic complications in childhood moyamoya disease. Neurosurgery 38:1120–1125, discussion 1125–1126PubMed
19.
go back to reference Jea A, Smith ER, Robertson R et al (2005) Moyamoya syndrome associated with Down syndrome: outcome after surgical revascularization. Pediatrics 116:e694–e701PubMedCrossRef Jea A, Smith ER, Robertson R et al (2005) Moyamoya syndrome associated with Down syndrome: outcome after surgical revascularization. Pediatrics 116:e694–e701PubMedCrossRef
20.
go back to reference Guzman R, Lee M, Achrol A et al (2009) Clinical outcome after 450 revascularisation procedures for moyamoya disease. J Neurosurg 111:927–935PubMedCrossRef Guzman R, Lee M, Achrol A et al (2009) Clinical outcome after 450 revascularisation procedures for moyamoya disease. J Neurosurg 111:927–935PubMedCrossRef
21.
go back to reference Ibrahimi DM, Tamargo AES (2010) Moyamoya disease in children. Child Nerv Syst 26:1297–1308CrossRef Ibrahimi DM, Tamargo AES (2010) Moyamoya disease in children. Child Nerv Syst 26:1297–1308CrossRef
22.
go back to reference Yilmaz EY, Pritz MD, Bruno A et al (2001) Moyamoya: Indiana University Medical Centre experience. Arch Neurol 58:1274–1278PubMedCrossRef Yilmaz EY, Pritz MD, Bruno A et al (2001) Moyamoya: Indiana University Medical Centre experience. Arch Neurol 58:1274–1278PubMedCrossRef
23.
go back to reference Chiu D, Shedden P, Bratina P, Grotta JC (1998) Clinical features of Moyamoya disease in the United States. Stroke 29:1347–1351PubMedCrossRef Chiu D, Shedden P, Bratina P, Grotta JC (1998) Clinical features of Moyamoya disease in the United States. Stroke 29:1347–1351PubMedCrossRef
24.
go back to reference Khan N, Schuknecht B, Boltshauser E et al (2003) Moyamoya disease and Moyamoya syndrome: experience in Europe; choice of revascularisation procedures. Acta Neurochir (Wien) 145:1061–1071CrossRef Khan N, Schuknecht B, Boltshauser E et al (2003) Moyamoya disease and Moyamoya syndrome: experience in Europe; choice of revascularisation procedures. Acta Neurochir (Wien) 145:1061–1071CrossRef
25.
go back to reference Darwish B, Besser M (2005) Long term outcome in children with Moyamoya disease: experience in 16 patients. J Clin Neurosci 12(8):873–877PubMedCrossRef Darwish B, Besser M (2005) Long term outcome in children with Moyamoya disease: experience in 16 patients. J Clin Neurosci 12(8):873–877PubMedCrossRef
26.
go back to reference Fryer RH, Anderson RC, Chiriboga CA, Feldstein NA (2003) Sickle cell anaemia with moyamoya disease: outcomes after EDAS procedure. Pediatr Neurol 29:124–130PubMedCrossRef Fryer RH, Anderson RC, Chiriboga CA, Feldstein NA (2003) Sickle cell anaemia with moyamoya disease: outcomes after EDAS procedure. Pediatr Neurol 29:124–130PubMedCrossRef
27.
go back to reference Hankinson TC, Bohman LE, Heyer G et al (2008) Surgical treatment of moyamoya syndrome in patients with sickle cell anaemia: outcome following encephaloduroarteriosynangiosis. J Neurosurg Pediatr 1:211–216PubMedCrossRef Hankinson TC, Bohman LE, Heyer G et al (2008) Surgical treatment of moyamoya syndrome in patients with sickle cell anaemia: outcome following encephaloduroarteriosynangiosis. J Neurosurg Pediatr 1:211–216PubMedCrossRef
28.
go back to reference Smith ER, McClain CD, Heeney M, Scott RM (2009) Pial synangiosis in patients with moyamoya syndrome and sickle cell anaemia: perioperative management and surgical outcome. Neurosurg Focus 26:E10PubMedCrossRef Smith ER, McClain CD, Heeney M, Scott RM (2009) Pial synangiosis in patients with moyamoya syndrome and sickle cell anaemia: perioperative management and surgical outcome. Neurosurg Focus 26:E10PubMedCrossRef
29.
go back to reference Roach ES, Golomb MR, Adams R et al (2008) Management of stroke in infants and children: a scientific statement from a Special Writing Group of the American Heart Association Stroke Council and the Council on Cardiovascular Disease in the Young. Stroke 39:2644–2691PubMedCrossRef Roach ES, Golomb MR, Adams R et al (2008) Management of stroke in infants and children: a scientific statement from a Special Writing Group of the American Heart Association Stroke Council and the Council on Cardiovascular Disease in the Young. Stroke 39:2644–2691PubMedCrossRef
Metadata
Title
Surgical revascularisation for childhood moyamoya
Authors
J. Ng
D. Thompson
J. P. S. Lumley
D. E. Saunders
V. Ganesan
Publication date
01-07-2012
Publisher
Springer-Verlag
Published in
Child's Nervous System / Issue 7/2012
Print ISSN: 0256-7040
Electronic ISSN: 1433-0350
DOI
https://doi.org/10.1007/s00381-012-1743-7

Other articles of this Issue 7/2012

Child's Nervous System 7/2012 Go to the issue