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Volume 26, Issue 1, Pages 133-136 (January 2010)


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Coronary artery bypass graft surgery depletes plasma thiamine levels

Michael W. Donnino, M.D.abCorresponding Author Informationemail address, Michael N. Cocchi, M.D.a, Howard Smithline, M.D.c, Erin Carney, B.A.a, Peter P. Chou, Ph.D.d, Justin Salciccoli, B.A.a

Received 10 February 2009; accepted 1 June 2009.

Abstract 

Objective

Thiamine is an essential component of cellular metabolism, and lack of this vitamin results in a potentially life-threatening biochemical lesion. The stress of surgery and critical disease depletes electrolytes, minerals, and essential biochemical substrates. We hypothesized that critical illness (represented by major surgery) would result in decreased thiamine levels over time.

Methods

We performed a prospective, observational study of serial thiamine levels of 15 patients who underwent non-emergent coronary artery bypass graft surgery. The primary endpoint was change in thiamine levels from before to immediately after surgery. Secondary endpoints included change in thiamine levels from presurgical to 6- and 24-h time points.

Results

Of the 15 study patients, 1 did not have a plasma thiamine measurement at time 0 because of laboratory error and could not be accounted for in paired comparisons over time. Plasma thiamine levels decreased significantly from before to after coronary artery bypass grafting (P=0.0004). In addition, there was a statistically significant decrease in thiamine levels from before surgery to 24h (P=0.003).

Conclusion

Our data suggest that major surgery (as a surrogate for the stress of critical illness) depletes thiamine levels; further study is needed to determine whether routine replacement of thiamine in the critically ill is warranted.

a Department of Emergency Medicine, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA

b Division of Critical Care Medicine, Department of Medicine, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA

c Department of Emergency Medicine, Baystate Medical Center, Springfield, Massachusetts, USA

d Quest Diagnostics Nichols Institute, Chantilly, Virginia, USA

Corresponding Author InformationCorresponding author. Tel.: +617-754-2323; fax: +617-754-2350.

 This project was funded from grant P30 DK040561 from the National Institutes of Health.

PII: S0899-9007(09)00250-0

doi:10.1016/j.nut.2009.06.004


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