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Trace element and vitamin concentrations and losses in critically ill patients treated with continuous venovenous hemofiltration
167
Citations
4
References
1999
Year
NutritionVitamin ConcentrationsCritical Care MedicineNutrient BioavailabilityRenal FunctionIntensive Care UnitHematologyClinical ChemistryPublic HealthTrace ElementMicronutrient SupplementationContinuous Venovenous HemofiltrationTransfusion MedicineClinical NutritionMicronutrientsCritical Care ManagementHemostasisMedicineNephrologyBlood TransfusionEmergency Medicine
Objectives To measure the blood concentrations of a number of trace elements and vitamins in critically ill patients and examine their elimination by continuous venovenous hemofiltration (CVVH). Setting Intensive care unit of a tertiary institution. Design Prospective, controlled, clinical study. Patients Eight critically ill patients requiring renal replacement therapy, nine patients requiring intensive care treatment but not requiring renal replacement therapy, and nine healthy controls. Interventions Measurement of trace element and vitamin concentrations in blood and ultrafiltrate. Measurements and Main Results Compared with normal volunteers, critically ill patients requiring CVVH had significantly lower median blood concentrations of vitamin C, vitamin E, selenium, and zinc. During the first 24 hrs of CVVH, there were no changes in the trace element and vitamin concentrations in blood, nor were there differences between pre- and postfilter samples. Micronutrient losses in the ultrafiltrate were small or undetectable except for Vitamin C, chromium, and copper. Compared with normal volunteers, critically ill patients not requiring CVVH also had significantly lower median blood concentrations of vitamin C, vitamin E, selenium, and zinc. There were no differences between the two critically ill groups. Conclusions The clinical significance of the reductions in blood concentrations of selenium, zinc, vitamin C, and vitamin E in critically ill patients and the ultrafiltrate losses of Vitamin C, copper, and chromium remains unclear. (Crit Care Med 1999; 27:220-223)
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