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August 20, 2013; 81 (8) Clinical/Scientific Notes

Propofol-related infusion syndrome heralding a mitochondrial disease: Case report

Martin Savard, Nicolas Dupré, Alexis F. Turgeon, Richard Desbiens, Stephan Langevin, Denis Brunet
First published July 19, 2013, DOI: https://doi.org/10.1212/WNL.0b013e3182a1aa78
Martin Savard
From the Department of Neurological Sciences (M.S., N.D., R.D., D.B.) and the Division of Critical Care Medicine, Department of Anesthesiology (A.F.T., S.L.), L'Enfant-Jésus Hospital, CHU de Québec; and Axe Traumatologie-Urgence-Soins Intensifs (Trauma–Emergency–Critical Care Medicine Unit), Université Laval, Québec, Canada.
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Nicolas Dupré
From the Department of Neurological Sciences (M.S., N.D., R.D., D.B.) and the Division of Critical Care Medicine, Department of Anesthesiology (A.F.T., S.L.), L'Enfant-Jésus Hospital, CHU de Québec; and Axe Traumatologie-Urgence-Soins Intensifs (Trauma–Emergency–Critical Care Medicine Unit), Université Laval, Québec, Canada.
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Alexis F. Turgeon
From the Department of Neurological Sciences (M.S., N.D., R.D., D.B.) and the Division of Critical Care Medicine, Department of Anesthesiology (A.F.T., S.L.), L'Enfant-Jésus Hospital, CHU de Québec; and Axe Traumatologie-Urgence-Soins Intensifs (Trauma–Emergency–Critical Care Medicine Unit), Université Laval, Québec, Canada.
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Richard Desbiens
From the Department of Neurological Sciences (M.S., N.D., R.D., D.B.) and the Division of Critical Care Medicine, Department of Anesthesiology (A.F.T., S.L.), L'Enfant-Jésus Hospital, CHU de Québec; and Axe Traumatologie-Urgence-Soins Intensifs (Trauma–Emergency–Critical Care Medicine Unit), Université Laval, Québec, Canada.
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Stephan Langevin
From the Department of Neurological Sciences (M.S., N.D., R.D., D.B.) and the Division of Critical Care Medicine, Department of Anesthesiology (A.F.T., S.L.), L'Enfant-Jésus Hospital, CHU de Québec; and Axe Traumatologie-Urgence-Soins Intensifs (Trauma–Emergency–Critical Care Medicine Unit), Université Laval, Québec, Canada.
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Denis Brunet
From the Department of Neurological Sciences (M.S., N.D., R.D., D.B.) and the Division of Critical Care Medicine, Department of Anesthesiology (A.F.T., S.L.), L'Enfant-Jésus Hospital, CHU de Québec; and Axe Traumatologie-Urgence-Soins Intensifs (Trauma–Emergency–Critical Care Medicine Unit), Université Laval, Québec, Canada.
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Citation
Propofol-related infusion syndrome heralding a mitochondrial disease: Case report
Martin Savard, Nicolas Dupré, Alexis F. Turgeon, Richard Desbiens, Stephan Langevin, Denis Brunet
Neurology Aug 2013, 81 (8) 770-771; DOI: 10.1212/WNL.0b013e3182a1aa78

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Propofol-related infusion syndrome (PRIS) is a rare but catastrophic complication of propofol use. It is clinically characterized by metabolic acidosis, rhabdomyolysis, arrhythmias, myocardial failure, renal failure, and hepatomegaly, and may lead to death.1 Some risk factors are associated with PRIS, namely young age, critical illness, high fat intake, catecholamine or steroid use, inborn error of fatty acid oxidation, propofol doses exceeding 4–5 mg/kg/hour, and duration of use exceeding 48 hours.1 Some evidence also suggests that PRIS is related to a mitochondrial toxicity of propofol.2,3

Acknowledgment

The authors thank Éric Laflamme for his help revising this manuscript.

Footnotes

  • Author contributions: Dr. Martin Savard: drafting/revising the manuscript for content, including medical writing for content, study concept or design, analysis or interpretation of data. Dr. Nicolas Dupré: drafting/revising the manuscript for content, including medical writing for content. Dr. Alexis F. Turgeon: drafting/revising the manuscript for content, including medical writing for content. Dr. Richard Desbiens: drafting/revising the manuscript for content, including medical writing for content. Dr. Stephan Langevin: drafting/revising the manuscript for content, including medical writing for content. Dr. Denis Brunet: drafting/revising the manuscript for content, including medical writing for content.

  • Study funding: No targeted funding reported.

  • Disclosure: M. Savard and N. Dupré report no disclosures. A. Turgeon is a recipient of a research career grant (salary support) from the Fonds de la Recherche du Québec–Santé (FRQ-S), and from the Canadian Institutes of Health Research (CIHR). No financial support was received for this article. R. Desbiens, S. Langevin, and D. Brunet report no disclosures. Go to Neurology.org for full disclosures.

  • Received December 19, 2012.
  • Accepted in final form April 11, 2013.
  • © 2013 American Academy of Neurology
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Letters: Rapid online correspondence

  • PRIS in mitochondrial disease : better safe than sorry?
    • Martin Savard, Neurologist, Department of Neurological Sciences, l'Enfant-Jesus Hospital, CHU de Quebecmartinsavard17@hotmail.com
    • Martin Savard, Quebec City, PQ, Canada; Alexis F. Turgeon, Quebec City, PQ, Canada
    Submitted August 14, 2013
  • Banning propofol in patients with mitochondrial disorders is unwarranted.
    • Jerome Parness, Professor, Dept of Anesthesiology, Children's Hospital of Pittsburgh of UPMCparnessj@upmc.edu
    Submitted August 07, 2013
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