Bolan Charles D, Cecco Stacey A, Yau Yu Ying, Wesley Robert A, Oblitas Jaime M, Rehak Nadja N, Leitman Susan F
Department of Transfusion Medicine, Warren Grant Magnuson Clinical Center, National Institutes of Health, Bethesda, Maryland 20892-1184, USA.
Transfusion. 2003 Oct;43(10):1414-22. doi: 10.1046/j.1537-2995.2003.00513.x.
The metabolic effects of oral calcium (Ca) supplementation during plateletpheresis were evaluated in a randomized, placebo-controlled trial.
Twenty-three donors underwent four plateletpheresis procedures each, receiving in random order, elemental Ca (Ca) 1 or 2 g orally, or a corresponding placebo, 30 minutes before donation. Ten of these donors underwent a fifth procedure using a 4-g Ca dose. All procedures were performed at a fixed citrate infusion rate of 1.5 mg per kg per minute.
Oral Ca induced dose-sensitive changes in parathyroid hormone (iPTH), total (tCa), and ionized (iCa) calcium levels. Compared to placebo, the greatest improvement in tCa and iCa levels occurred after the 2-g Ca dose (tCa of 73, 89, and 25% above placebo levels at 60 min, using 1, 2, and 4 g of oral Ca, respectively). Twenty-four hours after apheresis, serum tCa and iCa levels were higher, and iPTH levels lower, in donors who received oral Ca rather than placebo. Marked increases in urinary Ca and magnesium (Mg) excretion occurred at the completion of apheresis, were unaffected by Ca dose, and returned to baseline within 24 hours. Plateletpheresis also induced significant changes in serum alkaline phosphatase, 1,25-dihydroxyvitamin D, and osteocalcin levels immediately and at 24 hours after apheresis.
Plateletpheresis induces marked acute metabolic effects, with sustained changes evident up to 24 hours after the completion of apheresis. Oral Ca supplementation exerts a significant but clinically modest impact on selected laboratory variables associated with these effects. Further studies are indicated to examine the long-term impact of plateletpheresis, with or without Ca supplementation, on donor Ca balance and bone density.
在一项随机、安慰剂对照试验中评估了血小板单采过程中口服钙补充剂的代谢效应。
23名献血者每人接受4次血小板单采程序,在每次献血前30分钟随机顺序口服1克或2克元素钙(Ca)或相应的安慰剂。其中10名献血者使用4克钙剂量进行了第5次程序。所有程序均以每分钟每千克1.5毫克的固定枸橼酸盐输注速率进行。
口服钙引起甲状旁腺激素(iPTH)、总钙(tCa)和离子钙(iCa)水平的剂量敏感性变化。与安慰剂相比,2克钙剂量后tCa和iCa水平改善最大(在60分钟时,分别使用1克、2克和4克口服钙,tCa比安慰剂水平分别高出73%、89%和25%)。单采后24小时,接受口服钙而非安慰剂的献血者血清tCa和iCa水平较高,iPTH水平较低。单采结束时尿钙和镁(Mg)排泄显著增加,不受钙剂量影响,并在24小时内恢复至基线水平。血小板单采还在单采后即刻和24小时引起血清碱性磷酸酶、1,25-二羟维生素D和骨钙素水平的显著变化。
血小板单采引起明显的急性代谢效应,单采结束后长达24小时仍有持续变化。口服钙补充剂对与这些效应相关的特定实验室指标有显著但临床上适度的影响。有必要进一步研究以检查血小板单采(无论是否补充钙)对献血者钙平衡和骨密度的长期影响。