Børch K, Greisen G
Department of Neonatology, National University Hospital, Copenhagen, Denmark.
J Cereb Blood Flow Metab. 1997 Apr;17(4):448-54. doi: 10.1097/00004647-199704000-00010.
Studies on the kinetics of 99mTc-D,L-hexamethylpropylene amine oxime (99mTc-HMPAO) in adults have shown that it is not an ideal tracer of CBF because it underestimates high-flow areas. Knowledge of the kinetics of the tracer is important in evaluating the studies. The kinetics of 99mTc-HMPAO in infants may be different from that in adults, therefore, we examined the cerebral uptake and retention of 99mTc-HMPAO in neonates and estimated the degree of brain-to-blood back diffusion by comparing corresponding 133Xe flow images and 99mTc-HMPAO distribution images. In addition, we measured the urinary excretion of 99mTc-HMPAO. Regional CBF was measured using a mobile brain-dedicated, fast-rotating, four-head multidetector system specially designed for neonatal studies. Tracers were 99mTc-HMPAO (4 MBq/kg) and 133Xe (500 MBq/kg). Cerebral uptake and leak-out of 99mTc-HMPAO were measured by a single scintillation crystal placed over the frontoparietal part of the infant's head. The cerebral retention of 99mTc-HMPAO was analyzed in 50 infants. The mean gestational age and birth weight (95% confidence interval) were 34.4 weeks (32.2-35.7) and 2,326 g (1,954-2,995), respectively. The cerebral uptake of 99mTc-HMPAO was examined in 16 of the 50 infants, and activity during 24 h was monitored in five. In 11 infants, corresponding 133Xe studies were performed. Urinary excretion was studied in 12 infants. The maximal activity in the brain was reached 90s after i.v. injection and was 104% (98-111) of the stable level, which was reached approximately 3 min after the injection. The decay corrected leakout of the tracer during the following 24 h was 1.0% (0.4-1.5) per hour. The cerebral retention was calculated at 6.8% (6.1-7.6), highest in the group of ictal studies and lowest in premature infants with intracranial hemorrhage. The mean value of the fixation/clearance ratio alpha was estimated at 3.4 (2.8-4.4). The mean urinary excretion over 24 h was 19.5% (11.4-27.7) and was significantly related to renal function as indicated by serum urea (p = 0.02 r2 = 0.55). A four-compartment model describing the kinetics of 99mTc-HMPAO is shown to be valid in neonates. The cerebral retention of the tracer is higher in neonates because of higher extraction and lower initial back diffusion from brain to blood. In linearizing 99mTc-HMPAO distribution images, a smaller correction is necessary, and we propose a value of the correction factor of 3.4. In this way, 99mTc-HMPAO is a more reliable tracer of the distribution of CBF in neonates compared with adults. The urinary excretion is significantly reduced compared with adults, and the radiation dose to the bladder wall is reduced. The effective dose is 0.3 mSv/MBq/kg.
针对成人的99m锝-D,L-六甲基丙烯胺肟(99mTc-HMPAO)动力学研究表明,它并非理想的脑血流量(CBF)示踪剂,因为它会低估高血流区域。了解示踪剂的动力学对于评估研究很重要。99mTc-HMPAO在婴儿体内的动力学可能与成人不同,因此,我们研究了99mTc-HMPAO在新生儿脑中的摄取和滞留情况,并通过比较相应的133氙血流图像和99mTc-HMPAO分布图像来估计脑-血反向扩散程度。此外,我们测量了99mTc-HMPAO的尿排泄情况。使用专门为新生儿研究设计的移动脑专用、快速旋转、四头多探测器系统测量局部脑血流量。示踪剂为99mTc-HMPAO(4 MBq/kg)和133氙(500 MBq/kg)。通过放置在婴儿头部额顶部的单个闪烁晶体测量99mTc-HMPAO的脑摄取和泄漏情况。对50名婴儿的99mTc-HMPAO脑滞留情况进行了分析。平均胎龄和出生体重(95%置信区间)分别为34.4周(32.2 - 35.7)和2326克(1954 - 2995)。在50名婴儿中的16名中检测了99mTc-HMPAO的脑摄取情况,并对5名婴儿在24小时内的活性进行了监测。在1l名婴儿中进行了相应的133氙研究。对12名婴儿的尿排泄情况进行了研究。静脉注射后90秒时脑内活性达到最大值,为稳定水平的104%(98 - 111),稳定水平大约在注射后3分钟达到。在接下来的24小时内,示踪剂经衰变校正后的泄漏率为每小时1.0%(0.4 - 1.5)。脑滞留率计算为6.8%(6.1 - 7.6),在发作期研究组中最高,在颅内出血的早产儿中最低。固定/清除率α的平均值估计为3.4(2.8 - 4.4)。24小时内的平均尿排泄率为19.5%(11.4 - 27.7),并且如血清尿素所示,与肾功能显著相关(p = 0.02,r2 = 0.55)。一个描述99mTc-HMPAO动力学的四室模型在新生儿中被证明是有效的。由于摄取率较高且初始时从脑到血的反向扩散较低,示踪剂在新生儿脑中的滞留率更高。在将99mTc-HMPAO分布图像线性化时,需要较小的校正,我们提出校正因子的值为3.4。这样,与成人相比,99mTc-HMPAO是新生儿CBF分布更可靠的示踪剂。与成人相比,尿排泄显著减少,膀胱壁的辐射剂量降低。有效剂量为0.3 mSv/MBq/kg。