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    <subfield code="a">BMG</subfield>
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    <subfield code="a">eng</subfield>
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    <subfield code="a">Limbrick, David D. </subfield>
    <subfield code="e">Autor</subfield>
    <subfield code="9">54408</subfield>
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    <subfield code="a">Decompression with or without Duraplasty for Chiari I and Syringomyelia</subfield>
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    <subfield code="a">p&#xE1;ginas: 2015-2025</subfield>
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    <subfield code="a">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 (&#xB1;SD) syrinx reduction was 3.08&#xB1;2.33 mm and 1.22&#xB1;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.

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    <subfield code="a">ENFERMEDADES INFANTILES</subfield>
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    <subfield code="a">MEDICINA CL&#xCD;NICA HOSPITALARIA</subfield>
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    <subfield code="a">ORTOPEDIA GENERAL</subfield>
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    <subfield code="a">PEDIATR&#xCD;A GENERAL</subfield>
    <subfield code="9">54247</subfield>
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    <subfield code="a">TRASTORNOS DE LA COLUMNA VERTEBRAL</subfield>
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    <subfield code="a">NEUROLOG&#xCD;A</subfield>
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    <subfield code="a">NEUROCIRUG&#xCD;A GENERAL</subfield>
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    <subfield code="a">Shannon, Chevis N. </subfield>
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    <subfield code="a">Bayman, Emine O. </subfield>
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    <subfield code="a">Meehan, Thanda </subfield>
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    <subfield code="a">Kallem, Marisa </subfield>
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    <subfield code="a">Ackerman, Laurie L.</subfield>
    <subfield code="9">54415</subfield>
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    <subfield code="a">Adelson, P. David </subfield>
    <subfield code="9">54416</subfield>
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    <subfield code="a">Ahmed, Raheel </subfield>
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    <subfield code="a">Albert, Gregory </subfield>
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    <subfield code="a">Aldana, Philipp R. </subfield>
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    <subfield code="9">22665</subfield>
    <subfield code="d">Massachusetts NEJM Group</subfield>
    <subfield code="o">NEJM013</subfield>
    <subfield code="t">The New England Journal of Medicine </subfield>
    <subfield code="w">ESSALUD</subfield>
    <subfield code="x">0028-4793</subfield>
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    <subfield code="e">2026-08-28</subfield>
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