Neuroanesthesia Guidelines for Optimizing Transcranial Motor Evoked Potential Neuromonitoring During Deformity and Complex Spinal Surgery: A Delphi Consensus Study.


Journal

Spine
ISSN: 1528-1159
Titre abrégé: Spine (Phila Pa 1976)
Pays: United States
ID NLM: 7610646

Informations de publication

Date de publication:
01 Jul 2020
Historique:
entrez: 17 6 2020
pubmed: 17 6 2020
medline: 9 10 2020
Statut: ppublish

Résumé

Expert opinion-modified Delphi study. We used a modified Delphi approach to obtain consensus among leading spinal deformity surgeons and their neuroanesthesiology teams regarding optimal practices for obtaining reliable motor evoked potential (MEP) signals. Intraoperative neurophysiological monitoring of transcranial MEPs provides the best method for assessing spinal cord integrity during complex spinal surgeries. MEPs are affected by pharmacological and physiological parameters. It is the responsibility of the spine surgeon and neuroanesthesia team to understand how they can best maintain high-quality MEP signals throughout surgery. Nevertheless, varying approaches to neuroanesthesia are seen in clinical practice. We identified 19 international expert spinal deformity treatment teams. A modified Delphi process with two rounds of surveying was performed. Greater than 50% agreement on the final statements was considered "agreement"; >75% agreement was considered "consensus." Anesthesia regimens and protocols were obtained from the expert centers. There was a large amount of variability among centers. Two rounds of consensus surveying were performed, and all centers participated in both rounds of surveying. Consensus was obtained for 12 of 15 statements, and majority agreement was obtained for two of the remaining statements. Total intravenous anesthesia was identified as the preferred method of maintenance, with few centers allowing for low mean alveolar concentration of inhaled anesthetic. Most centers advocated for <150 μg/kg/min of propofol with titration to the lowest dose that maintains appropriate anesthesia depth based on awareness monitoring. Use of adjuvant intravenous anesthetics, including ketamine, low-dose dexmedetomidine, and lidocaine, may help to reduce propofol requirements without negatively effecting MEP signals. Spine surgeons and neuroanesthesia teams should be familiar with methods for optimizing MEPs during deformity and complex spinal cases. Although variability in practices exists, there is consensus among international spinal deformity treatment centers regarding best practices. 5.

Sections du résumé

STUDY DESIGN METHODS
Expert opinion-modified Delphi study.
OBJECTIVE OBJECTIVE
We used a modified Delphi approach to obtain consensus among leading spinal deformity surgeons and their neuroanesthesiology teams regarding optimal practices for obtaining reliable motor evoked potential (MEP) signals.
SUMMARY OF BACKGROUND DATA BACKGROUND
Intraoperative neurophysiological monitoring of transcranial MEPs provides the best method for assessing spinal cord integrity during complex spinal surgeries. MEPs are affected by pharmacological and physiological parameters. It is the responsibility of the spine surgeon and neuroanesthesia team to understand how they can best maintain high-quality MEP signals throughout surgery. Nevertheless, varying approaches to neuroanesthesia are seen in clinical practice.
METHODS METHODS
We identified 19 international expert spinal deformity treatment teams. A modified Delphi process with two rounds of surveying was performed. Greater than 50% agreement on the final statements was considered "agreement"; >75% agreement was considered "consensus."
RESULTS RESULTS
Anesthesia regimens and protocols were obtained from the expert centers. There was a large amount of variability among centers. Two rounds of consensus surveying were performed, and all centers participated in both rounds of surveying. Consensus was obtained for 12 of 15 statements, and majority agreement was obtained for two of the remaining statements. Total intravenous anesthesia was identified as the preferred method of maintenance, with few centers allowing for low mean alveolar concentration of inhaled anesthetic. Most centers advocated for <150 μg/kg/min of propofol with titration to the lowest dose that maintains appropriate anesthesia depth based on awareness monitoring. Use of adjuvant intravenous anesthetics, including ketamine, low-dose dexmedetomidine, and lidocaine, may help to reduce propofol requirements without negatively effecting MEP signals.
CONCLUSION CONCLUSIONS
Spine surgeons and neuroanesthesia teams should be familiar with methods for optimizing MEPs during deformity and complex spinal cases. Although variability in practices exists, there is consensus among international spinal deformity treatment centers regarding best practices.
LEVEL OF EVIDENCE METHODS
5.

Identifiants

pubmed: 32539292
doi: 10.1097/BRS.0000000000003433
pii: 00007632-202007010-00014
doi:

Substances chimiques

Anesthetics, Intravenous 0
Dexmedetomidine 67VB76HONO
Ketamine 690G0D6V8H
Lidocaine 98PI200987
Propofol YI7VU623SF

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

911-920

Références

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Auteurs

Corey T Walker (CT)

Department of Neurosurgery, Barrow Neurological Institute, St. Joseph's Hospital and Medical Center, Phoenix, AZ.

Han Jo Kim (HJ)

Department of Orthopedics, Hospital for Special Surgery, New York, NY.

Paul Park (P)

Department of Neurosurgery, University of Michigan, Ann Arbor, MI.

Lawrence G Lenke (LG)

Department of Orthopedics, Columbia University, New York, NY.

Mark A Weller (MA)

Department of Anesthesiology, Columbia University, New York, NY.

Justin S Smith (JS)

Department of Neurosurgery, University of Virginia, Charlottesville, VA.

Edward C Nemergut (EC)

Department of Anesthesiology, University of Virginia, Charlottesville, VA.

Daniel M Sciubba (DM)

Department of Neurosurgery, Johns Hopkins University, Baltimore, MD.

Michael Y Wang (MY)

Department of Neurosurgery, University of Miami, Miami, FL.

Christopher Shaffrey (C)

Department of Neurosurgery, Duke University, Durham, NC.

Vedat Deviren (V)

Department of Orthopedics, University of California-San Francisco, San Francisco, CA.

Praveen V Mummaneni (PV)

Department of Neurosurgery, University of California-San Francisco, San Francisco, CA.

Joyce M Chang (JM)

Department of Anesthesiology, University of California-San Francisco, San Francisco, CA.

Valli P Mummaneni (VP)

Department of Anesthesiology, University of California-San Francisco, San Francisco, CA.

Khoi D Than (KD)

Department of Neurosurgery, Oregon Health and Sciences University, Portland, Oregon.

Pedro Berjano (P)

Department of Orthopedics, Istituto Ortopedico Galeazzi, Milan, Italy.

Robert K Eastlack (RK)

Department of Orthopedics, Scripps Clinic, San Diego, CA.

Gregory M Mundis (GM)

Department of Orthopedics, Scripps Clinic, San Diego, CA.

Adam S Kanter (AS)

Department of Neurosurgery, University of Pittsburgh, Pittsburgh, PA.

David O Okonkwo (DO)

Department of Neurosurgery, University of Pittsburgh, Pittsburgh, PA.

John H Shin (JH)

Department of Neurosurgery, Massachusetts General Hospital, Boston, MA.

Jason M Lewis (JM)

Department of Anesthesiology, Massachusetts General Hospital, Boston, Massachusetts.

Tyler Koski (T)

Department of Neurosurgery, Northwestern University, Chicago, IL.

Daniel J Hoh (DJ)

Department of Neurosurgery, University of Florida, Gainesville, FL.

Steven D Glassman (SD)

Department of Orthopedics, University of Louisville, Louisville, KY.

Susan B Vinci (SB)

Northstar Anesthesia, Louisville, KY.

Alan H Daniels (AH)

Department of Orthopedics, Brown University, Providence, Rhode Island.

Claudia F Clavijo (CF)

Department of Anesthesiology, University of Colorado-Denver, Denver, CO.

Jay D Turner (JD)

Department of Neurosurgery, Barrow Neurological Institute, St. Joseph's Hospital and Medical Center, Phoenix, AZ.

Marc McLawhorn (M)

Valley Anesthesiology Consultants, Phoenix, AZ.

Juan S Uribe (JS)

Department of Neurosurgery, Barrow Neurological Institute, St. Joseph's Hospital and Medical Center, Phoenix, AZ.

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