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Comparison of posterior fossa decompression with or without duraplasty in children with Type I Chiari malformation.
Childs Nerv Syst. 2014 Aug; 30(8):1419-24.CN

Abstract

PURPOSE

Chiari malformation type I (CM1) is a common and often debilitating neurosurgical disease. Whether to treat CM1 patients with a traditional posterior fossa decompression with duraplasty (PFDD) or a less invasive extradural decompression (PFDO) is controversial. The purpose of this study was to compare clinical outcome and syrinx resolution between the two procedures.

METHODS

We retrospectively reviewed the records of 36 patients treated with PFDD and 29 patients with PFDO between 2003 and 2011. We compared baseline demographic, clinical, and radiographic characteristics. The primary clinical outcome was the Chicago Chiari Outcome Scale (CCOS). The primary radiographic outcome was qualitative syrinx improvement or resolution.

RESULTS

At baseline, age and sex distributions, radiographic characteristics, and presenting symptoms were similar in patients undergoing PFDD and PFDO. Patients undergoing PFDO had shorter surgical time (1.5 vs. 2.8 h; p < 0.001) and length of hospital stay (2.1 days compared to 3.3 days; p < 0.001). Cerebrospinal fluid-related complications were more common in patients receiving PFDD (7/36) than PFDO (0/29) (p = 0.014). Clinical improvement, defined by the mean CCOS score, was comparable in patients receiving PFDO (14.7) and PFDD (14.6) (p = 0.70). Among patients with postoperative syrinx imaging, 10/13 in the PFDD group improved or resolved, compared to 8/8 in the PFDO group (p = 0.26).

CONCLUSIONS

Extradural decompression for CM1 produces comparable rates of clinical and radiographic improvement as the more invasive decompression with duraplasty. Given the increased morbidity and resource utilization associated with PFDD, PFDO should be considered an attractive first-line option for most CM1 patients.

Authors+Show Affiliations

Department of Neurological Surgery, University of Washington School of Medicine, Seattle Children's Hospital, Seattle, WA, USA, amy.lee@seattlechildrens.org.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Comparative Study
Journal Article
Research Support, N.I.H., Extramural

Language

eng

PubMed ID

24777296

Citation

Lee, Amy, et al. "Comparison of Posterior Fossa Decompression With or Without Duraplasty in Children With Type I Chiari Malformation." Child's Nervous System : ChNS : Official Journal of the International Society for Pediatric Neurosurgery, vol. 30, no. 8, 2014, pp. 1419-24.
Lee A, Yarbrough CK, Greenberg JK, et al. Comparison of posterior fossa decompression with or without duraplasty in children with Type I Chiari malformation. Childs Nerv Syst. 2014;30(8):1419-24.
Lee, A., Yarbrough, C. K., Greenberg, J. K., Barber, J., Limbrick, D. D., & Smyth, M. D. (2014). Comparison of posterior fossa decompression with or without duraplasty in children with Type I Chiari malformation. Child's Nervous System : ChNS : Official Journal of the International Society for Pediatric Neurosurgery, 30(8), 1419-24. https://doi.org/10.1007/s00381-014-2424-5
Lee A, et al. Comparison of Posterior Fossa Decompression With or Without Duraplasty in Children With Type I Chiari Malformation. Childs Nerv Syst. 2014;30(8):1419-24. PubMed PMID: 24777296.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Comparison of posterior fossa decompression with or without duraplasty in children with Type I Chiari malformation. AU - Lee,Amy, AU - Yarbrough,Chester K, AU - Greenberg,Jacob K, AU - Barber,Jason, AU - Limbrick,David D, AU - Smyth,Matthew D, Y1 - 2014/04/29/ PY - 2014/04/09/received PY - 2014/04/10/accepted PY - 2014/4/30/entrez PY - 2014/4/30/pubmed PY - 2015/3/10/medline SP - 1419 EP - 24 JF - Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery JO - Childs Nerv Syst VL - 30 IS - 8 N2 - PURPOSE: Chiari malformation type I (CM1) is a common and often debilitating neurosurgical disease. Whether to treat CM1 patients with a traditional posterior fossa decompression with duraplasty (PFDD) or a less invasive extradural decompression (PFDO) is controversial. The purpose of this study was to compare clinical outcome and syrinx resolution between the two procedures. METHODS: We retrospectively reviewed the records of 36 patients treated with PFDD and 29 patients with PFDO between 2003 and 2011. We compared baseline demographic, clinical, and radiographic characteristics. The primary clinical outcome was the Chicago Chiari Outcome Scale (CCOS). The primary radiographic outcome was qualitative syrinx improvement or resolution. RESULTS: At baseline, age and sex distributions, radiographic characteristics, and presenting symptoms were similar in patients undergoing PFDD and PFDO. Patients undergoing PFDO had shorter surgical time (1.5 vs. 2.8 h; p < 0.001) and length of hospital stay (2.1 days compared to 3.3 days; p < 0.001). Cerebrospinal fluid-related complications were more common in patients receiving PFDD (7/36) than PFDO (0/29) (p = 0.014). Clinical improvement, defined by the mean CCOS score, was comparable in patients receiving PFDO (14.7) and PFDD (14.6) (p = 0.70). Among patients with postoperative syrinx imaging, 10/13 in the PFDD group improved or resolved, compared to 8/8 in the PFDO group (p = 0.26). CONCLUSIONS: Extradural decompression for CM1 produces comparable rates of clinical and radiographic improvement as the more invasive decompression with duraplasty. Given the increased morbidity and resource utilization associated with PFDD, PFDO should be considered an attractive first-line option for most CM1 patients. SN - 1433-0350 UR - https://www.unboundmedicine.com/medline/citation/24777296/Comparison_of_posterior_fossa_decompression_with_or_without_duraplasty_in_children_with_Type_I_Chiari_malformation_ DB - PRIME DP - Unbound Medicine ER -