Hébert P, Mehta N, Wang J, Hindmarsh T, Jones G, Cardinal P
Department of Pathology, Ottawa General Hospital, University of Ottawa, ON, Canada.
Crit Care Med. 1997 May;25(5):749-55. doi: 10.1097/00003246-199705000-00007.
To determine the feasibility of the magnesium-loading test in the critically ill and to validate serum ionized magnesium assay using the magnesium-loading test as a reference in this same patient population.
Double-blind, randomized, controlled clinical investigation.
Tertiary level intensive care unit.
Forty-four consecutive critically ill patients without evidence of renal insufficiency.
Patients were randomly allocated to receive 30 mmol (7.5 g) of magnesium sulfate daily for 3 days, or an equivalent amount of normal saline.
We recorded baseline characteristics, and serial serum biochemical measurements included creatinine, glucose, sodium, potassium, phosphate, total calcium, ionized calcium, total magnesium, and ionized magnesium. Serum assays were accompanied by 24-hr urine collections of creatinine and magnesium over the 3-day period. Baseline characteristics were comparable in both groups. In patients receiving magnesium, serum ionized magnesium and total magnesium concentrations were increased by 43% (p = .0001) and 59% (p = .0002), respectively, on day 1 as compared with the control group. Magnesium excretion in the control group averaged 4.8 +/- 2.3 mmol/day during the 3-day study period, while the magnesium excretion in the magnesium-loaded group was significantly increased to 22.7 +/- 10.9 mmol/day (p < .0001). Following day 1 magnesium loading, patients who excreted < 70% of the total magnesium (30 mmol infused magnesium plus 4.8 mmol basal excretion) were termed as functionally magnesium-deficient retainers (n = 12), and patients who excreted > 70% of the total magnesium were termed as nonretainers (n = 7). In addition, magnesium retainers on day 2 (nine of ten patients) and day 3 (five of six patients) excreted > 70% of the total magnesium, indicating a replenishment of body magnesium stores. In contrast, nonretainers on day 2 (four of five patients), and day 3 (four of four patients) continued to excrete excess amounts of magnesium. In the retainer group, only two patients had a low serum ionized magnesium concentration, while two other patients had low total serum magnesium values. In addition, magnesium retention was associated with low ionized calcium and high phosphate values.
The magnesium-loading test is feasible and appears to be valid based on its performance during the 3-day evaluation. Using the magnesium-loading test as a reference, serum ionized magnesium appears to be an insensitive biochemical marker of functional hypomagnesemia. Larger cohort studies using the magnesium-loading test will help establish the true prevalence of magnesium deficiency and its associated risk factors in critically ill patients.
确定镁负荷试验在危重症患者中的可行性,并验证在同一患者群体中以镁负荷试验为参考的血清离子镁检测方法。
双盲、随机、对照临床研究。
三级重症监护病房。
44例连续入住的无肾功能不全证据的危重症患者。
患者被随机分配,一组每天接受30 mmol(7.5 g)硫酸镁,共3天,另一组接受等量生理盐水。
记录基线特征,系列血清生化检测指标包括肌酐、葡萄糖、钠、钾、磷酸盐、总钙、离子钙、总镁和离子镁。在3天期间,血清检测同时收集24小时尿肌酐和尿镁。两组基线特征具有可比性。与对照组相比,接受镁治疗的患者在第1天血清离子镁和总镁浓度分别升高了43%(p = .0001)和59%(p = .0002)。在3天的研究期间,对照组镁排泄平均为4.8±2.3 mmol/天,而镁负荷组镁排泄显著增加至22.7±10.9 mmol/天(p < .0001)。在第1天镁负荷后,排泄的镁少于总镁量(输注的30 mmol镁加上4.8 mmol基础排泄量)70%的患者被称为功能性镁缺乏潴留者(n = 12),排泄的镁超过总镁量70%的患者被称为非潴留者(n = 7)。此外,第2天(10例患者中的9例)和第3天(6例患者中的5例)的镁潴留者排泄的镁超过总镁量的70%,表明机体镁储备得到补充。相比之下,第2天(5例患者中的4例)和第3天(4例患者中的4例)的非潴留者继续排泄过量镁。在潴留组中,只有2例患者血清离子镁浓度低,另外2例患者血清总镁值低。此外,镁潴留与低离子钙和高磷酸盐值相关。
基于3天评估期间的表现,镁负荷试验是可行的且似乎是有效的。以镁负荷试验为参考,血清离子镁似乎是功能性低镁血症的不敏感生化标志物。使用镁负荷试验的更大队列研究将有助于确定危重症患者镁缺乏的真实患病率及其相关危险因素。