Morbidity and mortality in the surgical treatment of six hundred five pediatric patients with isthmic or dysplastic spondylolisthesis.

dc.contributor.author

Fu, Kai-Ming G

dc.contributor.author

Smith, Justin S

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Polly, David W

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Perra, Joseph H

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Sansur, Charles A

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Berven, Sigurd H

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Broadstone, Paul A

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Choma, Theodore J

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Goytan, Michael J

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Noordeen, Hilali H

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Knapp, D Raymond

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Hart, Robert A

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Donaldson, William F

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Boachie-Adjei, Oheneba

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Shaffrey, Christopher I

dc.date.accessioned

2023-10-11T18:36:27Z

dc.date.available

2023-10-11T18:36:27Z

dc.date.issued

2011-02

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2023-10-11T18:36:26Z

dc.description.abstract

Study design

Retrospective analysis of prospectively collected database.

Objective

To analyze the rate of complications, including neurologic deficits, associated with operative treatment of pediatric isthmic and dysplastic spondylolisthesis.

Summary of background data

Pediatric isthmic and dysplastic spondylolisthesis are relatively uncommon dis-orders. Several prior studies have suggested a high rate of complication associated with operative intervention. How-ever, most of these studies were performed with sufficiently small sample sizes such that the presence of one complication could significantly affect the overall rate. The Scoliosis Research Society (SRS) prospectively collects morbidity and mortality (M&M) data from its members. This multicentered, multisurgeon database permits analysis of the surgical treatment of this relatively rare condition on an aggregate scale and provides surgeons with useful information for preoperative counseling.

Methods

Patients who underwent surgical treatment for isthmic or dysplastic spondylolisthesis from 2004 to 2007 were identified from the SRS M&M database. Inclusion criteria for analysis included age ≤ 21 and a primary diagnosis of isthmic or dysplastic spondylolisthesis.

Results

Of 25,432 pediatric cases reported, there were a total of 605 (2.4%) cases of pediatric dysplastic (n ∇ 62, 10%) and isthmic (n ∇ 543, 90%) spondylolisthesis, with a mean age of 15 years (range, 4-21). Approximately 50% presented with neural element compression, and less than 1% of cases were revisions. Surgical procedures included fusions in 92%, osteotomies in 39%, and reductions in 38%. The overall complication rate was 10.4%. The most common complications included postoperative neurologic deficit (n ∇ 31, 5%), dural tear (n ∇ 8, 1.3%), and wound infection (n ∇ 12, 2%). Perioperative deep venous thrombosis and pulmonary embolus were reported in 2 (0.3%) and 1 (0.2%) patients, respectively. There were no deaths in this series.

Conclusion

Pediatric isthmic and dysplastic spondylolisthesis are relatively uncommon disorders, representing only 2.4% of pediatric spine procedures in the present study. Even among experienced spine surgeons, surgical treatment of these spinal conditions is associated with a relatively high morbidity.
dc.identifier.issn

0362-2436

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1528-1159

dc.identifier.uri

https://hdl.handle.net/10161/29247

dc.language

eng

dc.publisher

Ovid Technologies (Wolters Kluwer Health)

dc.relation.ispartof

Spine

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10.1097/brs.0b013e3181cf3a1d

dc.subject

Humans

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Surgical Wound Infection

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Spondylolisthesis

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Nervous System Diseases

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Postoperative Complications

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Treatment Outcome

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Orthopedic Procedures

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Morbidity

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Survival Rate

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Retrospective Studies

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Databases, Factual

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Adolescent

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Child

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Child, Preschool

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Young Adult

dc.title

Morbidity and mortality in the surgical treatment of six hundred five pediatric patients with isthmic or dysplastic spondylolisthesis.

dc.type

Journal article

duke.contributor.orcid

Shaffrey, Christopher I|0000-0001-9760-8386

pubs.begin-page

308

pubs.end-page

312

pubs.issue

4

pubs.organisational-group

Duke

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School of Medicine

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Clinical Science Departments

pubs.organisational-group

Orthopaedic Surgery

pubs.organisational-group

Neurosurgery

pubs.publication-status

Published

pubs.volume

36

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