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  <titleInfo>
    <title>Decompression with or without Duraplasty for Chiari I and Syringomyelia</title>
  </titleInfo>
  <name type="personal">
    <namePart>Limbrick, David D.</namePart>
    <role>
      <roleTerm authority="marcrelator" type="text">creator</roleTerm>
    </role>
    <role>
      <roleTerm type="text">Autor</roleTerm>
    </role>
  </name>
  <name type="personal">
    <namePart>Shannon, Chevis N.</namePart>
  </name>
  <name type="personal">
    <namePart>Bayman, Emine O.</namePart>
  </name>
  <name type="personal">
    <namePart>Meehan, Thanda</namePart>
  </name>
  <name type="personal">
    <namePart>Kallem, Marisa</namePart>
  </name>
  <name type="personal">
    <namePart>Ackerman, Laurie L.</namePart>
  </name>
  <name type="personal">
    <namePart>Adelson, P. David</namePart>
  </name>
  <name type="personal">
    <namePart>Ahmed, Raheel</namePart>
  </name>
  <name type="personal">
    <namePart>Albert, Gregory</namePart>
  </name>
  <name type="personal">
    <namePart>Aldana, Philipp R.</namePart>
  </name>
  <typeOfResource>text</typeOfResource>
  <originInfo>
    <place>
      <placeTerm type="code" authority="marccountry">pe</placeTerm>
    </place>
    <issuance>monographic</issuance>
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  <language>
    <languageTerm authority="iso639-2b" type="code">spa</languageTerm>
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  <language>
    <languageTerm authority="iso639-2b" type="code">eng</languageTerm>
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    <form authority="marcform">print</form>
    <extent>páginas: 2015-2025</extent>
  </physicalDescription>
  <abstract>Background: In children with Chiari type I malformation and syringomyelia, neurosurgical posterior fossa decompression (PFD) provides clinical improvement, but whether duraplasty (incising the dura and placing a dural graft) improves outcomes is unclear. Methods: We conducted a multicenter, cluster-randomized, controlled trial of PFD with duraplasty (PFD-D) as compared with PFD alone. Persons 21 years of age or younger with cerebellar tonsillar ectopia of at least 5 mm and a maximum syrinx diameter of 3.0 to 9.9 mm were enrolled at 38 centers. Centers were cluster-randomized: all the participants within each center underwent the same intervention. The primary outcome was surgical complications within 6 months. Secondary outcomes were clinical improvement, syrinx reduction, and repeat decompression at 10 to 24 months and the change in overall health-related quality of life at 6 to 24 months. Results: A total of 162 participants were included in the trial, of whom 78 were assigned to undergo PFD-D and 84 to undergo PFD alone. The percentage of participants with complications within 6 months was 14% with PFD-D and 6% with PFD (adjusted odds ratio, 2.59; 95% confidence interval [CI], 0.86 to 7.84; P=0.11). At 24 months, the percentage of participants with clinical improvement was 58% with PFD-D and 46% with PFD; the mean (±SD) syrinx reduction was 3.08±2.33 mm and 1.22±1.79 mm, respectively; and the percentage of participants with repeat decompression was 3% and 14%. Changes in health-related quality of life were similar in the two groups. Conclusions: The percentage of participants with surgical complications did not differ significantly between those who underwent PFD-D and those who underwent PFD alone. Larger trials are needed to determine the relative benefits and risks of these two procedures.

</abstract>
  <subject>
    <topic>ENFERMEDADES INFANTILES</topic>
  </subject>
  <subject>
    <topic>MEDICINA CLÍNICA HOSPITALARIA</topic>
  </subject>
  <subject>
    <topic>ORTOPEDIA GENERAL</topic>
  </subject>
  <subject>
    <topic>PEDIATRÍA GENERAL</topic>
  </subject>
  <subject>
    <topic>TRASTORNOS DE LA COLUMNA VERTEBRAL</topic>
  </subject>
  <subject>
    <topic>NEUROLOGÍA</topic>
  </subject>
  <subject>
    <topic>NEUROCIRUGÍA GENERAL</topic>
  </subject>
  <relatedItem type="host">
    <titleInfo>
      <title>The New England Journal of Medicine</title>
    </titleInfo>
    <originInfo>
      <publisher>Massachusetts NEJM Group</publisher>
    </originInfo>
    <identifier>NEJM013</identifier>
    <identifier type="issn">0028-4793</identifier>
    <identifier type="local">ESSALUD</identifier>
  </relatedItem>
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    <recordContentSource authority="marcorg">BMG</recordContentSource>
    <recordCreationDate encoding="marc">      </recordCreationDate>
    <recordChangeDate encoding="iso8601">20260902145039.0</recordChangeDate>
    <recordIdentifier>ESSALUD</recordIdentifier>
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