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Klippel-Feil: A constellation of diagnoses, a contemporary presentation, and recent national trends.

Authors :
Zhou PL
Poorman GW
Wang C
Pierce KE
Bortz CA
Alas H
Brown AE
Tishelman JC
Janjua MB
Vasquez-Montes D
Moon J
Horn SR
Segreto F
Ihejirika YU
Diebo BG
Passias PG
Source :
Journal of craniovertebral junction & spine [J Craniovertebr Junction Spine] 2019 Jul-Sep; Vol. 10 (3), pp. 133-138.
Publication Year :
2019

Abstract

Background: Klippel-Feil syndrome (KFS) includes craniocervical anomalies, low posterior hairline, and brevicollis, with limited cervical range of motion; however, there remains no consensus on inheritance pattern. This study defines incidence, characterizes concurrent diagnoses, and examines trends in the presentation and management of KFS.<br />Methods: This was a retrospective review of the Kid's Inpatient Database (KID) for KFSpatients aged 0-20 years from 2003 to 2012. Incidence was established using KID-supplied year and hospital-trend weights. Demographics and secondary diagnoses associated with KFS were evaluated. Comorbidities, anomalies, and procedure type trends from 2003 to 2012 were assessed for likelihood to increase among the years studied using ANOVA tests.<br />Results: Eight hundred and fifty-eight KFS diagnoses (age: 9.49 years; 51.1% females) and 475 patients with congenital fusion (CF) (age: 8.33 years; 50.3% females) were analyzed. We identified an incidence rate of 1/21,587 discharges. Only 6.36% of KFS patients were diagnosed with Sprengel's deformity; 1.44% with congenital fusion. About 19.1% of KFS patients presented with another spinal abnormality and 34.0% presented with another neuromuscular anomaly. About 36.51% of KFS patients were diagnosed with a nonspinal or nonmusculoskeletal anomaly, with the most prevalent anomalies being of cardiac origin (12.95%). About 7.34% of KFS patients underwent anterior fusions, whereas 6.64% of KFS patients underwent posterior fusions. The average number of levels operated on was 4.99 with 8.28% receiving decompressions. Interbody devices were used in 2.45% of cases. The rate of fusions with <3 levels (7.46%) was comparable to that of 3 levels or greater (7.81%).<br />Conclusions: KFS patients were more likely to have other spinal abnormalities (19.1%) and nonnervous system abnormalities (13.63%). Compared to congenital fusions, KFS patients were more likely to have congenital abnormalities such as Sprengel's deformity. KFS patients are increasingly being treated with spinal fusion.<br />Level of Evidence: III.<br />Competing Interests: There are no conflicts of interest.<br /> (Copyright: © 2019 Journal of Craniovertebral Junction and Spine.)

Details

Language :
English
ISSN :
0974-8237
Volume :
10
Issue :
3
Database :
MEDLINE
Journal :
Journal of craniovertebral junction & spine
Publication Type :
Academic Journal
Accession number :
31772424
Full Text :
https://doi.org/10.4103/jcvjs.JCVJS_65_19