Chiari malformation type I surgery in children: French multicenter 10-year cohort

Author:

Mazerand Edouard1,Benichi Sandro2,Taverne Maxime3,Paternoster Giovanna24,Rolland Alice5,Antherieu Pierre6,Todeschi Julien7,Kamdem Noumoye Lawrence8,Gilard Vianney9,Bretonnier Maxime10,Fournier Luc Le1,Jecko Vincent8,Gimbert Edouard8,Proust François7,Boetto Sergio6,Roujeau Thomas5,James Syril211,Khonsari Roman H.312,Riffaud Laurent10,Delion Matthieu1,Zerah Michel211,Scavarda Didier4

Affiliation:

1. Department of Neurosurgery, Angers University Hospital, Angers;

2. Department of Pediatric Neurosurgery, Necker–Enfants Malades Hospital, Assistance Publique—Hôpitaux de Paris;

3. Craniofacial Growth and Form, Necker–Enfants Malades Hospital, Assistance Publique—Hôpitaux de Paris;

4. Department of Pediatric Neurosurgery, CHU Timone Enfant, Marseille, France

5. Department of Pediatric Neurosurgery, Montpellier University Hospital, Montpellier;

6. Department of Neurosurgery, Toulouse University Hospital, Toulouse;

7. Department of Neurosurgery, Strasbourg University Hospital, Strasbourg;

8. Department of Pediatric Neurosurgery, Bordeaux University Hospital, Bordeaux;

9. Department of Neurosurgery, Rouen University Hospital, Rouen;

10. Department of Neurosurgery, Rennes University Hospital, Rennes;

11. Department of Neurosurgery, French Reference Center for Chiari and Rare Vertebral and Medullary Malformations (C-MAVEM), Montpellier University Hospital, Montpellier;

12. Department of Pediatric Maxillofacial and Plastic Surgery, Necker–Enfants Malades Hospital, Assistance Publique—Hôpitaux de Paris; and

Abstract

OBJECTIVE Chiari malformation type I (CM-I) is frequent in children and remains a surgical challenge. Several techniques have been described for posterior fossa decompression. No decision algorithm has been validated, and strategies are highly variable between institutions. The goal of this study was to define therapeutic guidelines that take into consideration patient specificities. METHODS The authors retrospectively collected data from patients who were < 18 years of age, were diagnosed with CM-I, and were treated surgically between 2008 and 2018 in 8 French pediatric neurosurgical centers. Data on clinical features, morphological parameters, and surgical techniques were collected. Clinical outcomes at 3 and 12 months after surgery were assessed by the Chicago Chiari Outcome Scale. The authors used a hierarchical clustering method to define clusters of patients by considering their anatomical similarities, and then compared outcomes between surgical strategies in each of these clusters. RESULTS Data from 255 patients were collected. The mean age at surgery was 9.6 ± 5.0 years, syringomyelia was reported in 60.2% of patients, the dura mater was opened in 65.0% of patients, and 17.3% of patients underwent a redo surgery for additional treatment. The mean Chicago Chiari Outcome Scale score was 14.4 ± 1.5 at 3 months (n = 211) and 14.6 ± 1.9 at 12 months (n = 157). The hierarchical clustering method identified three subgroups with potentially distinct mechanisms underlying tonsillar herniation: bony compression, basilar invagination, and foramen magnum obstruction. Each cluster matched with specific outcomes. CONCLUSIONS This French multicenter retrospective cohort study enabled the identification of three subgroups among pediatric patients who underwent surgery for CM-I, each of which was associated with specific outcomes. This morphological classification of patients might help in understanding the underlying mechanisms and providing personalized treatment.

Publisher

Journal of Neurosurgery Publishing Group (JNSPG)

Subject

General Medicine

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