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   <subfield code="a">10.1007/BF01411256</subfield>
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   <subfield code="a">(NATIONALLICENCE)springer-10.1007/BF01411256</subfield>
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   <subfield code="a">The surgical treatment of Chiari I malformation</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[J. Klekamp, U. Batzdorf, M. Samii, H. Bothe]</subfield>
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   <subfield code="a">Summary: A retrospective study was undertaken on 133 patients with a Chiari I malformation treated within the last 16 years at the Departments of Neurosurgery at the Nordstadt Hospital Hannover, Germany, and the University of California, Los Angeles, U.S.A. Ninety-seven patients presented with symptoms related to accompanying syringomyelia and 4 with associated syringobulbia. They underwent 149 surgical procedures and were followed for a mean of 39±52 months. A decompression at the foramen magnum was performed in 124 patients, while 22 of those with syringomyelia were treated by shunting (7 syringosubarachnoid shunts, 15 syringoperitoneal or -pleural shunts), and 3 by ventriculoperitoneal shunts for hydrocephalus. Except for ventriculoperitoneal shunting, at least a short-term decrease in size of an associated syrinx was observed for all procedures in the majority of cases. However, no long-term benefit was observed for syrinx shunting operations. The best clinical longterm results were obtained with decompression of the foramen magnum in patients with (86% free of a clinical recurrence) and without syringomyelia (77% free of a clinical recurrence). We advise against syrinx shunting, a large craniectomy, and obex plugging which are associated with higher recurrence rates. Instead, surgery should consist of a small craniectomy, opening of the dura, archnoid dissection to establish normal cerebrospinal fluid (CSF) outflow from the 4th ventricle, and a fascia lata durai graft.</subfield>
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   <subfield code="a">Springer-Verlag, 1996</subfield>
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   <subfield code="a">Chiari malformation</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">syringomyelia</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">cerebrospinal fluid</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">extracellular fluid</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Klekamp</subfield>
   <subfield code="D">J.</subfield>
   <subfield code="u">Medical School of Hannover, Neurosurgical Clinic, Nordstadt Hospital Hannover, Germany</subfield>
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   <subfield code="a">Batzdorf</subfield>
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   <subfield code="u">Division of Neurosurgery, University of California, Los Angeles, CA, USA</subfield>
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   <subfield code="a">Samii</subfield>
   <subfield code="D">M.</subfield>
   <subfield code="u">Medical School of Hannover, Neurosurgical Clinic, Nordstadt Hospital Hannover, Germany</subfield>
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   <subfield code="a">Bothe</subfield>
   <subfield code="D">H.</subfield>
   <subfield code="u">Medical School of Hannover, Neurosurgical Clinic, Nordstadt Hospital Hannover, Germany</subfield>
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  <datafield tag="773" ind1="0" ind2=" ">
   <subfield code="t">Acta Neurochirurgica</subfield>
   <subfield code="d">Springer-Verlag</subfield>
   <subfield code="g">138/7(1996-07-01), 788-801</subfield>
   <subfield code="x">0001-6268</subfield>
   <subfield code="q">138:7&lt;788</subfield>
   <subfield code="1">1996</subfield>
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   <subfield code="D">1</subfield>
   <subfield code="a">research-article</subfield>
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   <subfield code="B">NATIONALLICENCE</subfield>
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   <subfield code="u">https://doi.org/10.1007/BF01411256</subfield>
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   <subfield code="a">Bothe</subfield>
   <subfield code="D">H.</subfield>
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   <subfield code="B">NATIONALLICENCE</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
   <subfield code="b">Springer special CC-BY-NC licence</subfield>
   <subfield code="2">nationallicence</subfield>
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