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Mortality in Early-Onset Scoliosis During the Growth-friendly Surgery Era.
Guzek, Ryan H; Murphy, Robert; Hardesty, Christina K; Emans, John B; Garg, Sumeet; Smith, John T; Roye, Benjamin D; Glotzbecker, Michael P; Sturm, Peter F; Snyder, Brian D; Poon, Selina C; Poe-Kochert, Connie; Anari, Jason B.
Afiliación
  • Guzek RH; Children's Hospital of Philadelphia, Philadelphia, PA.
  • Murphy R; Medical University of South Carolina, Charleston, SC.
  • Hardesty CK; Rainbow Babies and Children's Hospital, Cleveland.
  • Emans JB; Boston Children's Hospital, Boston, MA.
  • Garg S; University of Colorado, Aurora, CO.
  • Smith JT; Primary Children's Hospital, Salt Lake City, UT.
  • Roye BD; Columbia University Medical Center, New York, NY.
  • Glotzbecker MP; Rainbow Babies and Children's Hospital, Cleveland.
  • Sturm PF; Cincinnati Children's Hospital and Medical Center, Cincinnati, OH.
  • Snyder BD; Boston Children's Hospital, Boston, MA.
  • Poon SC; Shriners for Children Medical Center, Pasadena, CA.
  • Poe-Kochert C; Rainbow Babies and Children's Hospital, Cleveland.
  • Anari JB; Children's Hospital of Philadelphia, Philadelphia, PA.
J Pediatr Orthop ; 42(3): 131-137, 2022 Mar 01.
Article en En | MEDLINE | ID: mdl-35138296
ABSTRACT

INTRODUCTION:

Early-onset scoliosis (EOS) is a spinal deformity that occurs in patients 9 years of age or younger. Severe deformity may result in thoracic insufficiency, respiratory failure, and premature death. The purpose of this study is to describe the modern-day natural history of mortality in patients with EOS.

METHODS:

The multicenter Pediatric Spine Study Group database was queried for all patients with EOS who are deceased, without exclusion. Demographics, underlying diagnoses, EOS etiology, operative and nonoperative treatments or observation, complications, and date of death were retrieved. Descriptive statistics and survival analysis with Kaplan-Meier curves were performed.

RESULTS:

There were 130/8009 patients identified as deceased for a registry mortality rate of 16 per 1000 patients. The mean age at death was 10.6 years (range 1.0 to 30.2 y) and the most common EOS etiology was neuromuscular (73/130, 56.2%; P<0.001). Deceased patients were more likely be treated operatively than nonoperatively or observed (P<0.001). The mean age of death for patients treated operatively (12.3 y) was older than those treated nonoperatively (7.0 y) or observed (6.3 y) (P<0.001) despite a larger deformity and similar index visit body mass index and ventilation requirements. Kaplan-Meier analysis confirmed an increased survival time in patients with a history of any spine operation compared with patients without a history of spine operation (P<0.0001). Operatively treated patients experienced a median of 3.0 complications from diagnosis to death. Overall, cardiopulmonary related complications were the most common (129/271, 47.6%; P<0.001), followed by implant-related (57/271, 21.0%) and wound-related (26/271, 9.6%). The primary cause of death was identified for 78/130 (60.0%) patients, of which 57/78 (73.1%) were cardiopulmonary related.

CONCLUSIONS:

This study represents the largest collection of EOS mortality to date, providing surgeons with a modern-day examination of the effects of surgical intervention to better council patients and families. Both fatal and nonfatal complications in children with EOS are most likely to involve the cardiopulmonary system. LEVEL OF EVIDENCE Level IV-therapeutic.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Escoliosis Tipo de estudio: Observational_studies / Prognostic_studies Límite: Child / Humans Idioma: En Revista: J Pediatr Orthop Año: 2022 Tipo del documento: Article País de afiliación: Panamá

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Escoliosis Tipo de estudio: Observational_studies / Prognostic_studies Límite: Child / Humans Idioma: En Revista: J Pediatr Orthop Año: 2022 Tipo del documento: Article País de afiliación: Panamá