The safety and efficacy of steroid treatment for acute spinal cord injury: A Systematic Review and meta-analysis.

Acute spinal cord injury Adverse effects Endocrine system Hyperglycemia Intensive care medicine Methylprednisolone Neurology Neuroscience Neurosurgery Pneumonia Spinal cord injury Steroids Trauma

Journal

Heliyon
ISSN: 2405-8440
Titre abrégé: Heliyon
Pays: England
ID NLM: 101672560

Informations de publication

Date de publication:
Feb 2020
Historique:
received: 04 09 2019
revised: 17 11 2019
accepted: 12 02 2020
entrez: 26 2 2020
pubmed: 26 2 2020
medline: 26 2 2020
Statut: epublish

Résumé

The role for steroids in acute spinal cord injury (ASCI) remains unclear; while some studies have demonstrated the risks of steroids outweigh the benefits,a meta-analyses conducted on heterogeneous patient populations have shown significant motor improvement at short-term but not at long-term follow-up. Given the heterogeneity of the patient population in previous meta-analyses and the publication of a recent trial not included in these meta-analyses, we sought to re-assess and update the safety and short-term and long-term efficacy of steroid treatment following ASCI in a more homogeneous patient population. A literature search was conducted on PubMed, EMBASE and Cochrane Library through June 2019 for studies evaluating the utility of steroids within the first 8 h following ASCI. Neurological and safety outcomes were extracted for patients treated and not treated with steroids. Pooled effect estimates were calculated using the random-effects model. Twelve studies, including five randomized controlled trials (RCTs) and seven observational studies (OBSs), were meta-analyzed. Overall, methylprednisolone was not associated with significant short-term or long-term improvements in motor or neurological scores based on RCTs or OBSs. An increased risk of hyperglycemia was shown in both RCTs (RR: 13.7; 95% CI: 1.93, 97.4; 1 study) and OBSs (RR: 2.9; 95% CI: 1.55, 5.41; 1 study). Risk for pneumonia was increased with steroids; while this increase was not statistically significant in the RCTs (pooled RR: 1.16; 95% C.I: 0.59, 2.29; 3 studies), it reached statistical significance in the OBSs (pooled RR: 2.00; 95% C.I: 1.32, 3.02; 6 studies). There was no statistically significant increased risk of gastrointestinal bleeding, decubitus ulcers, surgical site infections, sepsis, atelectasis, venous thromboembolism, urinary tract infections, or mortality among steroid-treated ASCI patients compared to untreated controls in either RCTs or OBSs. Methylprednisolone therapy within the first 8 h following ASCI failed to show a statistically significant short-term or long-term improvement in patients' overall motor or neurological scores compared to controls who were not administered steroids. For the same comparison, there was an increased risk of pneumonia and hyperglycemia compared to controls. Routine use of methylprednisone following ASCI should be carefully considered in the context of these results.

Identifiants

pubmed: 32095652
doi: 10.1016/j.heliyon.2020.e03414
pii: S2405-8440(20)30259-0
pii: e03414
pmc: PMC7033344
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

e03414

Informations de copyright

© 2020 Published by Elsevier Ltd.

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Auteurs

Ihtisham Sultan (I)

School of Pharmacy, MCPHS University, Boston, Massachusetts, USA.

Nayan Lamba (N)

Harvard Medical School, Boston, MA, USA.
Department of Neurosurgery, Computational Neuroscience Outcomes Center, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.

Aaron Liew (A)

National University of Ireland, Galway (NUIG), Galway, Ireland.

Phoung Doung (P)

School of Pharmacy, MCPHS University, Boston, Massachusetts, USA.

Ishaan Tewarie (I)

Department of Neurosurgery, Computational Neuroscience Outcomes Center, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.

James J Amamoo (JJ)

School of Pharmacy, MCPHS University, Boston, Massachusetts, USA.

Laxmi Gannu (L)

School of Pharmacy, MCPHS University, Boston, Massachusetts, USA.

Shreya Chawla (S)

Department of Neurosurgery, Computational Neuroscience Outcomes Center, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.

Joanne Doucette (J)

School of Pharmacy, MCPHS University, Boston, Massachusetts, USA.

Christian D Cerecedo-Lopez (CD)

Department of Neurosurgery, Computational Neuroscience Outcomes Center, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.

Stefania Papatheodorou (S)

Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA.

Ian Tafel (I)

Department of Neurosurgery, Computational Neuroscience Outcomes Center, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.

Linda S Aglio (LS)

Department of Neurosurgery, Computational Neuroscience Outcomes Center, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Department of Anesthesiology, Perioperative and Pain Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.

Timothy R Smith (TR)

Department of Neurosurgery, Computational Neuroscience Outcomes Center, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.

Hasan Zaidi (H)

Department of Neurosurgery, Computational Neuroscience Outcomes Center, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.

Rania A Mekary (RA)

School of Pharmacy, MCPHS University, Boston, Massachusetts, USA.
Department of Neurosurgery, Computational Neuroscience Outcomes Center, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA.

Classifications MeSH