Evidence map›Paper›PMID 42336348›Full record

ReviewArquivos de neuro-psiquiatria2026

Rhabdomyolysis: a narrative review.

Celia Harumi Tengan, Acary Souza Bulle Oliveira, Alzira Alves de Siqueira Carvalho, Cezar Daniel Snak de Souza, Claudia Ferreira da Rosa Sobreira, Edmar Zanoteli, Helga Cristina Almeida da Silva

Abstract readReview
In one paragraph

Review in Arquivos de neuro-psiquiatria, 2026. 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
–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

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

7 authors.

Celia Harumi TenganUniversidade Federal de São Paulo, Escola Paulista de Medicina, Departamento de Neurologia, São Paulo SP, Brazil.ORCID 0000-0001-6209-2332
Acary Souza Bulle OliveiraUniversidade Federal de São Paulo, Escola Paulista de Medicina, Departamento de Neurologia, São Paulo SP, Brazil.ORCID 0000-0002-6986-4937
Alzira Alves de Siqueira CarvalhoCentro Universitário Faculdade de Medicina do ABC (FMABC), Faculdade de Medicina, Departamento de Neurologia, São Paulo SP, Brazil.ORCID 0000-0002-5485-7937
Cezar Daniel Snak de SouzaUniversidade Federal de São Paulo, Escola Paulista de Medicina, Departamento de Anestesiologia, São Paulo SP, Brazil.ORCID 0000-0002-0464-3332
Claudia Ferreira da Rosa SobreiraUniversidade de São Paulo, Faculdade de Medicina de Ribeirão Preto, Departamento de Neurociências e Ciências do Comportamento, Ribeirão Preto SP, Brazil.ORCID 0000-0002-7420-1644
Edmar ZanoteliUniversidade de São Paulo, Faculdade de Medicina, Departamento de Neurologia, São Paulo SP, Brazil.ORCID 0000-0002-4991-6760
Helga Cristina Almeida da SilvaUniversidade Federal de São Paulo, Escola Paulista de Medicina, Departamento de Anestesiologia, São Paulo SP, Brazil.ORCID 0000-0002-9372-7019

Funding

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - Brazil (CAPES) Finance Code 001Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) 1996/02222-3Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) 2021/06180-7
6 · The paper itself

Abstract

Abstract: Rhabdomyolysis is the acute necrosis of striated skeletal muscle, with release of its constituents into the extracellular space and circulation. Acute muscle pain (myalgia), weakness, and edema are associated with serum levels of the muscle enzyme creatine kinase (CK) above 1,000 IU/L or 5 times the upper limit of the normal value. This narrative review provides an overview of the clinical and laboratory findings, etiology, treatment, and prevention of rhabdomyolysis in humans. Additionally, we highlighted the main syndromes and muscular disorders associated with rhabdomyolysis: 1. Clinical syndromes: neuroleptic malignant syndrome, serotoninergic syndrome, sympathomimetic syndrome, malignant hyperthermia, and anesthesia-induced rhabdomyolysis; and 2. Myopathies: toxic myopathies, idiopathic inflammatory myopathies, muscular dystrophies, ion channel diseases, glycogen storage diseases, fatty acid beta oxidation defects, and mitochondrial myopathies.

Indexed as

RhabdomyolysisCreatine KinaseHumansCreatine Kinase

Identifiers

PMID42336348
PMCPMC13290370

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.