Evidence map›Paper›PMID 41393776›Full record

ArticleSpine surgery and related research2025

Morbidity and Mortality of Pediatric Spinal Deformity Surgery Using the Japanese Orthopedic Association National Registry/Japanese Society for Spine Surgery and Related Research Database (JOANR/JSSR-DB).

Hideyuki Arima, Takumi Takeuchi, Yu Yamato, Tomoyuki Asada, Satoru Demura, Toru Doi, Akira Matsumura, Hiroki Oba, Ryo Sugawara, Satoshi Suzuki and 4 more

Abstract read
In one paragraph

Article in Spine surgery and related research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

14 authors.

Hideyuki ArimaRegistry and Outcome Committee, Japanese Scoliosis Society, Tokyo, Japan.
Takumi TakeuchiRegistry and Outcome Committee, Japanese Scoliosis Society, Tokyo, Japan.
Yu YamatoRegistry and Outcome Committee, Japanese Scoliosis Society, Tokyo, Japan.
Tomoyuki AsadaRegistry and Outcome Committee, Japanese Scoliosis Society, Tokyo, Japan.
Satoru DemuraRegistry and Outcome Committee, Japanese Scoliosis Society, Tokyo, Japan.
Toru DoiRegistry and Outcome Committee, Japanese Scoliosis Society, Tokyo, Japan.
Akira MatsumuraRegistry and Outcome Committee, Japanese Scoliosis Society, Tokyo, Japan.
Hiroki ObaRegistry and Outcome Committee, Japanese Scoliosis Society, Tokyo, Japan.
Ryo SugawaraRegistry and Outcome Committee, Japanese Scoliosis Society, Tokyo, Japan.
Satoshi SuzukiRegistry and Outcome Committee, Japanese Scoliosis Society, Tokyo, Japan.
Shinji TakahashiRegistry and Outcome Committee, Japanese Scoliosis Society, Tokyo, Japan.
Haruki UedaRegistry and Outcome Committee, Japanese Scoliosis Society, Tokyo, Japan.
Kei WatanabeRegistry and Outcome Committee, Japanese Scoliosis Society, Tokyo, Japan.
Naobumi HosoganeRegistry and Outcome Committee, Japanese Scoliosis Society, Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The Japanese Scoliosis Society conducted a survey on the complications of pediatric spinal deformity surgeries in 2012, 2014, and 2017. However, a registry-based survey was necessary to systematically and comprehensively identify complications, and a web-based registry system was established. This study aimed to investigate the frequency of pediatric spinal deformity surgeries and perioperative complications in Japan in 2022, using a web-based registry. Methods: Of the 158,263 cases collected from 1,032 institutions, 1,945 (485 boys and 1,460 girls) were included in the study. The diagnoses were idiopathic scoliosis (64.9%), congenital scoliosis (10.1%), neuromuscular scoliosis (7.4%), congenital kyphoscoliosis (1.1%), and others (16.5%). The intraoperative, postoperative (within 30 days), and systemic (within 30 days postoperatively) complications were investigated. Results: The overall complication rate was 6.0% (intraoperative, 2.5%; postoperative, 2.4%; and systemic, 2.0%). The complication rates by diagnosis were highest in congenital kyphosis (25.0%), followed by congenital kyphoscoliosis (18.2%) and neuromuscular scoliosis (13.3%), whereas idiopathic scoliosis (10-18 years old) had a complication rate of 3.7%. The most common intraoperative complications were massive bleeding (>2,000 mL) in 0.9%, dural tears in 0.7%, and nerve injury in 0.2% of the patients. The most frequent postoperative complications were neurologic deficits (0.8%), surgical site infections (0.8%), and implant failure (0.5%). The most frequent postoperative systemic complications were respiratory (0.6%) and urinary (0.4%). Conclusions: This nationwide web-based registry study provides a highly comprehensive report on pediatric scoliosis surgery in Japan in 2022. The complication rates were notably high for congenital kyphosis, congenital kyphoscoliosis, and neuromuscular scoliosis. These findings may help improve patient and family understanding of the risks associated with various spinal deformities and support shared decision-making in pediatric surgical care.

Indexed as

case registrynationwide surveypediatric scoliosis surgeryperioperative complication

Identifiers

PMID41393776
PMCPMC12696460

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LicenceCC BY-NC-ND
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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.