3.1. Patients
The current cross sectional study was undertaken in all of the patients admitted and stayed at least 2 days in Shahid Beheshti hospital ICU from February 2011 to March 2012. A total of 101 patients who met the inclusion criteria were enrolled in the study. Exclusion criteria were as follows: hemoglobin level of less than 10 g/dL, receiving blood products, Mg or Ca infusion before sampling, and receiving oral Mg supplementations. Moreover, the patients who were discharged in the day 1 of ICU stay were excluded.
To avoid the selection bias, the patients who fulfilled the criteria for critical illness and were newly admitted to ICU were enrolled. The level of Mg in serum was measured in such patients. In all cases, a complete history was taken, physical examination was performed, and findings related to the disease were evaluated.
All characteristics of the patients including age, gender, medical history, vital signs, route of feeding in ICU, medical history related to etiology (including GI disease, hypertension, and diabetes), drug abuse (especially diuretics, ACE inhibitors, and chemotherapy drugs), and blood pH were recorded.
Oral and parenteral Mg intake, medication use, severe diarrhea, steatorrhea, and smoking were statistically considered as confounding variables within the regression. Also, overestimation, underestimation, and poor recall might have confounded the results.
In the third day of admission, electrolyte profile including serum levels of Ca, sodium (Na), K, Mg, phosphor (P), blood urea nitrogen (BUN), and creatinine (Cr) were measured. After draining 5 mL of blood, clotting, and centrifuging, the separated serum was collected at -20°C, and Mg level was measured by the xylidyl blue method. The normal range of Mg is 1.8 to 2.5 mg/dL. Serum Mg level of < 1.70 mg/dL was considered as hypomagnesemia and ≥ 2.56 mg/dL as hypermagnesemia.
The results of laboratory testing, medical history, physical examinations, and findings related to the disease were recorded in a checklist. All of the patients were followed-up until discharge from the hospital.
The primary endpoint was to investigate the association of serum levels of Mg and mortality. Secondary endpoints included the relationship between Mg changes and clinical factors associated with the outcomes of patients admitted to ICU.