Congress of Neurological Surgeons Systematic Review and Evidence-Based Guidelines for Patients With Chiari Malformation: Surgical Interventions

Author:

Pattisapu Jogi V.1,Ackerman Laurie L.2,Infinger Libby Kosnik3,Maher Cormac O.4,Quinsey Carolyn5,Rocque Brandon G.6,Silberstein Howard7,Jackson Eric M.8,Jernigan Sarah9,Niazi Toba10,Qaiser Rabia11,Raskin Jeffrey S.12,Vachhrajani Shobhan13,Bauer David F.1415

Affiliation:

1. Pediatric Neurosurgery, University of Central Florida College of Medicine, Orlando, Florida, USA;

2. Department of Neurological Surgery, Indiana University Health, Indianapolis, Indiana, USA;

3. Department of Neurosurgery, Medical University of South Carolina (MUSC), Charleston, South Carolina, USA;

4. Department of Neurosurgery, Stanford Medicine, Palo Alto, California, USA;

5. Department of Neurosurgery, University of North Carolina Chapel Hill, Chapel Hill, North Carolina, USA;

6. Division of Pediatric Neurosurgery, Department of Neurosurgery, University of Alabama at Birmingham, Birmingham, Alabama, USA;

7. Department of Neurosurgery, University of Rochester School of Medicine and Dentistry, Rochester, New York, USA;

8. Department of Neurosurgery, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA;

9. Carolina Neurosurgery & Spine Associates, Charlotte, North Carolina, USA;

10. Department of Neurological Surgery, Nicklaus Children's Hospital, Miami, Florida, USA;

11. Department of Neurological Surgery, Indiana University School of Medicine, Indianapolis, Indiana, USA;

12. Department of Neurological Surgery, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA;

13. Department of Pediatrics, Wright State University Boonshoft School of Medicine, Dayton, Ohio, USA;

14. Department of Neurosurgery, Baylor College of Medicine, Houston, Texas, USA;

15. Division of Pediatric Neurosurgery, Texas Children's Hospital, Houston, Texas, USA

Abstract

BACKGROUND: Chiari malformation type I (CIM) diagnoses have increased in recent years. Controversy regarding the best operative management prompted a review of the literature to offer guidance on surgical interventions. OBJECTIVE: To assess the literature to determine (1) whether posterior fossa decompression or posterior fossa decompression with duraplasty is more effective in preoperative symptom resolution; (2) whether there is benefit from cerebellar tonsillar resection/reduction; (3) the role of intraoperative neuromonitoring; (4) in patients with a syrinx, how long should a syrinx be observed for improvement before additional surgery is performed; and 5) what is the optimal duration of follow-up care after preoperative symptom resolution. METHODS: A systematic review was performed using the National Library of Medicine/PubMed and Embase databases for studies on CIM in children and adults. The most appropriate surgical interventions, the use of neuromonitoring, and clinical improvement during follow-up were reviewed for studies published between 1946 and January 23, 2021. RESULTS: A total of 80 studies met inclusion criteria. Posterior fossa decompression with or without duraplasty or cerebellar tonsil reduction all appeared to show some benefit for symptom relief and syrinx reduction. There was insufficient evidence to determine whether duraplasty or cerebellar tonsil reduction was needed for specific patient groups. There was no strong correlation between symptom relief and syringomyelia resolution. Many surgeons follow patients for 6–12 months before considering reoperation for persistent syringomyelia. No benefit or harm was seen with the use of neuromonitoring. CONCLUSION: This evidence-based clinical guidelines for the treatment of CIM provide 1 Class II and 4 Class III recommendations. In patients with CIM with or without syringomyelia, treatment options include bone decompression with or without duraplasty or cerebellar tonsil reduction. Improved syrinx resolution may potentially be seen with dural patch grafting. Symptom resolution and syrinx resolution did not correlate directly. Reoperation for a persistent syrinx was potentially beneficial if the syrinx had not improved 6 to 12 months after the initial operation. The full guidelines can be seen online at https://www.cns.org/guidelines/browse-guidelines-detail/3-surgical-interventions.

Funder

Congress of Neurological Surgeons

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical),Surgery

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