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Experiences of surgical complications and reoperations in nonsyndromic sagittal synostosis patients in Oulu.
Svalina, Anja; Serlo, Willy; Sinikumpu, Juha-Jaakko; Salokorpi, Niina.
Afiliação
  • Svalina A; Research Unit of Clinical Medicine, Oulu University Hospital and University of Oulu, Oulu, Finland. asvalina@student.oulu.fi.
  • Serlo W; Medical Research Center, Oulu University Hospital, Oulu, Finland. asvalina@student.oulu.fi.
  • Sinikumpu JJ; Department of Neurosurgery, NeurocenterOulu University Hospital, PO Box 21, 90029, Oulu, OYS, Finland. asvalina@student.oulu.fi.
  • Salokorpi N; Research Unit of Clinical Medicine, Oulu University Hospital and University of Oulu, Oulu, Finland.
Childs Nerv Syst ; 2024 Jun 28.
Article em En | MEDLINE | ID: mdl-38940955
ABSTRACT

OBJECTIVE:

The purpose of this study was to evaluate the surgical complications of patients treated for nonsyndromic sagittal craniosynostosis and the necessity for reoperations due to craniocerebral disproportion. MATERIALS AND

METHODS:

The patient cohort of this study consisted of patients (N = 82) who were treated in the Oulu University Hospital using the open vault cranioplasty with a modified H-technique between the years 2008 to 2022. There were 69 males (84.1%) and 13 females (15.9%). The mean age at the primary operation was 6.1 months. Mean follow-up time was 9.0 years.

RESULTS:

There were no major complications related to the procedures. Two patients (2.4%) had a minor dural lesion. There were no postoperative wound infections. Of the 82 patients, seven patients with primary craniosynostosis (13.0%) developed symptomatic craniocerebral disproportion requiring reoperation to increase intracranial volume. In all these patients, invasive intracranial pressure (ICP) monitoring was performed prior to decision-making. In the majority of cases, the aesthetical outcome was considered good or excellent.

CONCLUSION:

The operative method used was feasible and safe. Thirteen percent of patients who were followed over 5 years required major surgery due to development of craniocerebral disproportion later in life.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Childs Nerv Syst / Childs nerv. syst / Childs nervous system Assunto da revista: NEUROLOGIA / PEDIATRIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Finlândia

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Childs Nerv Syst / Childs nerv. syst / Childs nervous system Assunto da revista: NEUROLOGIA / PEDIATRIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Finlândia