Nutrition
Volume 25, Issue 2 , Pages 142-146, February 2009

Wernicke's syndrome during parenteral feeding: Not an unusual complication

  • Francesco Francini-Pesenti, M.D.

      Affiliations

    • Clinical Nutrition Unit, Department of Clinical and Experimental Medicine, Azienda Ospedaliera, Padova, Italy
    • Corresponding Author InformationCorresponding author. Tel.: +39-498-212-346; fax: +39-482-821-1374
  • ,
  • Filippo Brocadello, M.D.

      Affiliations

    • Clinical Nutrition Unit, Department of Clinical and Experimental Medicine, Azienda Ospedaliera, Padova, Italy
  • ,
  • Renzo Manara, M.D.

      Affiliations

    • Neuroradiology Unit, Azienda Ospedaliera, Padova, Italy
  • ,
  • Luca Santelli, M.D.

      Affiliations

    • Department of Neurosciences, Azienda Ospedaliera, Padova, Italy
  • ,
  • Alice Laroni, M.D.

      Affiliations

    • Department of Neurosciences, Azienda Ospedaliera, Padova, Italy
  • ,
  • Lorenza Caregaro, M.D.

      Affiliations

    • Clinical Nutrition Unit, Department of Clinical and Experimental Medicine, Azienda Ospedaliera, Padova, Italy

Received 6 March 2008; accepted 6 August 2008. published online 20 October 2008.

Abstract 

Objective

Wernicke's encephalopathy (WE) is an acute disorder due to thiamine deficiency, characterized by ophthalmoplegia, ataxia, and mental confusion, similar to that classically observed in alcoholism. Some cases of WE were reported to coincide with other conditions such as hyperemesis gravidarum, bariatric surgery, and total parenteral nutrition. In this study the objective was to retrospectively evaluate the prevalence of WE among intravenously fed patients in our hospital during the previous 2 y.

Methods

Among all cases of WE diagnosed by cranial magnetic resonance scan during a 2-y period in the Azienda Ospedaliera of Padua, we identified patients who exhibited WE during parenteral feeding. Albumin plasma levels, measured at the onset of WE symptoms, were used to estimate nutritional status.

Results

We found seven cases of WE that coincided with intravenous feeding. WE occurred, on average, 13 d after the start of glucose infusion. The five subjects with albumin plasma levels lower than 35 g/L at the onset of WE received glucose infusion for fewer days. In six cases the clinical signs disappeared the day after thiamine infusion. In one case mental function did not normalize and the patient developed Korsakoff's syndrome despite prolonged thiamine treatment.

Conclusion

During a 2-y period we observed a high prevalence of WE in intravenously fed patients due to lack of thiamine supplementation. A prophylactic treatment must be performed in at-risk patients and multivitamin infusion containing thiamine must be administered daily during the course of intravenous feeding.

Keywords: Wernicke's encephalopathy, Thiamine, Total parenteral nutrition

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PII: S0899-9007(08)00354-7

doi:10.1016/j.nut.2008.08.003

Nutrition
Volume 25, Issue 2 , Pages 142-146, February 2009