Patients who suffer Alcohol Use Disorder (AUD) have a 30-80% incidence of thiamine deficiency causing Wernicke's Encephalopathy (WE). Intravenous (IV) thiamine replacement is standard practice in the treatment of alcoholic patients presenting to the Accident \& Emergency (A\&E) department, however routine co-supplementation with magnesium (administered IV as magnesium sulphate ), which is required as a co-factor for thiamine in some metabolic processes, e. g. on the activity of the enzyme transketolase in red blood cells, is not routine practice in the treatment of these patients. Without correction of concomitant magnesium deficiency there may be impaired utilisation of thiamine resulting in a failure to treat WE. This study is designed to determine if administration of magnesium to AUD patients affects red cell transketolasae and serum lactate concentrations by itself, or only acts to increase the effect of thiamine on the activity of this enzyme.
This is a 3- arm randomised, open label, controlled study in a cohort of alcoholic patients admitted through A\&E. Patients will be randomised to concurrent infusion of one of the following: * Arm 1: IV thiamine * Arm 2: IV magnesium sulphate followed by delayed IV thiamine * Arm 3: IV thiamine and IV magnesium sulphate Thiamine will be administered as IV Pabrinex, a compound preparation which also contains B vitamins and vitamin C. Administration of IV Pabrinex is standard care in this patient group and magnesium sulphate is routinely co-administered at Glasgow Royal Infirmary.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
127
Intravenous (Magnesium Sulphate) MgSO4 2 grams IV over 20 minutes
standard treatment
Glasgow Royal Infirmary
Glasgow, United Kingdom
Change in Erythrocyte transketolase activity
this is a biochemical marker of thiamine activity measured in units per gram of haemoglobin
Time frame: 0 and 2 hours
Change in serum lactate
Biochemical marker of metabolic dysfunction (expressed as mmol/L)
Time frame: 0 and 2 hours
Change in rate of resolution of alcohol withdrawal syndrome
time
Time frame: days
lactate dehydrogenase
biochemical (expressed in mmol/L)
Time frame: 0 and 2 hours
pre and post magnesium
biochemical (expressed in mmol/L)
Time frame: 0 and 2 hours
pre and post red cell thiamine
biochemical
Time frame: 0 and 2 hours
establish baseline micronutrient status of patients with alcohol withdrawal syndrome
biochemical
Time frame: o and 2 hours
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.