Evidence map›Paper›PMID 38858335›Full record

ArticleSpine deformity2024

How will early onset scoliosis surgery affect my child's future as a young adult? A follow-up study using patient-reported outcome measures.

Dmitri A Falkner, Kyle J Miller, John B Emans, George H Thompson, John T Smith, Jack M Flynn, Jeffrey R Sawyer

Abstract read
In one paragraph

Article in Spine deformity, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Dmitri A FalknerCampbell Clinic, Department of Orthopaedics, University of Tennessee, Campbell Clinic, 1211 Union Avenue, Suite 510, Memphis, TN, 38104, USA.
Kyle J MillerCampbell Clinic, Department of Orthopaedics, University of Tennessee, Campbell Clinic, 1211 Union Avenue, Suite 510, Memphis, TN, 38104, USA.
John B EmansBoston Children's Hospital, Boston, MA, USA.
George H ThompsonPediatric Spine Study Group, University Health-Rainbow Babies and Children's Hospital, Cleveland, OH, USA.
John T SmithUniversity of Utah, Salt Lake City, UT, USA.
Jack M FlynnChildren's Hospital of Philadelphia, Philadelphia, PA, USA.
Jeffrey R SawyerCampbell Clinic, Department of Orthopaedics, University of Tennessee, Campbell Clinic, 1211 Union Avenue, Suite 510, Memphis, TN, 38104, USA. jsawyer@campbellclinic.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeUsing patient-reported outcome measures (PROMs), this study was undertaken to determine how well patients with early onset scoliosis (EOS) fare in adulthood.

methodsAmong eight healthcare centers, 272 patients (≥ 18 years) surgically managed for EOS (≥ 5 years) completed the Scoliosis Research Society (SRS)-22r, Functional Assessment of Chronic Illness Therapy-10 (FACIT-Dyspnea-10), and Short Form (SF)-12. Functional and demographic data were collected.

resultsThe response rate was 40% (108/272). EOS etiologies were congenital (45%), neuromuscular (20%), idiopathic (20%) syndromic (11%), and unknown (4%). All patients scored within normal limits on the FACIT-Dyspnea-10 pulmonary (no breathing aids, 78%; no oxygen, 92%). SF-12 physical health scores and most SRS-22r domains were significantly decreased (p < 0.05 and p < 0.001, respectively) compared with normative values. SF-12 and SRS-22r mental health scores (MHS) were lower than normative values (p < 0.05 and p < 0.02, respectively). Physical health PROMs varied between etiologies. Treatment varied by etiology. Patients with congenital EOS were half as likely to undergo definitive fusion. There was no difference between EOS etiologies in SF-12 MHS, with t scores being slightly lower than normative peers.

conclusionGood long-term physical and social function and patient-reported quality of life were noted in surgically managed patients. Patients with idiopathic EOS physically outperformed those with other etiologies in objective and PROM categories but had similar MHS PROMs. Compared to normative values, EOS patients demonstrated decreased long-term physical capacity, slightly lower MHS, and preserved cardiopulmonary function. LEVEL OF EVIDENCE: Level IV Case Series.

Indexed as

Patient Reported Outcome MeasuresScoliosisAdolescentAdultAge of OnsetChildChild, PreschoolFemaleFollow-Up StudiesHumansMaleQuality of LifeYoung AdultEarly onset scoliosisHealth-related quality of lifeIdiopathic scoliosisSpine surgery

Identifiers

PMID38858335
PMCPMC11499523

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.