Dhawan V, Belakhlef A, Robeson W, Ishikawa T, Margouleff C, Takikawa S, Chaly T, Kazumata K, Margouleff D, Eidelberg D
Department of Neurology, Research and Medicine, North Shore University Hospital/Cornell University Medical College, Manhasset, New York 11030, USA.
J Nucl Med. 1996 Nov;37(11):1850-2.
PET, in conjunction with 18F-fluorodopa (FDOPA), has become the standard technique to assess basal ganglia degeneration in patients with movement disorders. Based on published dosimetry data, the injected dose of FDOPA is limited to 111 Mbq (3 mCi) because of exposure to the bladder wall, which is the critical organ for such studies. These dosimetry studies are based on mathematical models for the bladder radioactivity accumulation and clearance when the subjects were asked to void approximately 2 hr after the intravenous injection of FDOPA. In this study, we improved the radiation dose estimate to the bladder wall using dynamic PET to image the bladder during the uptake phase as well as before and after voiding.
The subjects were tested on a new protocol. They were hydrated preinjection and given a first bladder void break at 40 min postinjection and a second void at the end of study at 120 min.
The MIRD model, applied to the data collected from 10 adults of both sexes, yielded an average absorbed dose of 0.15 +/- 0.08 mGy/MBq (0.57 +/- 0.28 rad/mCi).
This absorbed dose is significantly lower than previous estimates and allows for FDOPA injections up to 333 Mbq (9 mCi).
正电子发射断层扫描(PET)结合18F - 氟多巴(FDOPA)已成为评估运动障碍患者基底神经节变性的标准技术。根据已发表的剂量学数据,由于膀胱壁是此类研究的关键器官,FDOPA的注射剂量限制在111兆贝可(3毫居里)。这些剂量学研究基于静脉注射FDOPA后约2小时受试者排尿时膀胱放射性积累和清除的数学模型。在本研究中,我们使用动态PET在摄取期以及排尿前后对膀胱进行成像,改进了对膀胱壁的辐射剂量估计。
受试者按照新方案进行测试。在注射前进行水化处理,并在注射后40分钟进行第一次膀胱排尿,在研究结束时120分钟进行第二次排尿。
将医学内照射剂量(MIRD)模型应用于从10名成年男女收集的数据,得出平均吸收剂量为0.15±0.08毫戈瑞/兆贝可(0.57±0.28拉德/毫居里)。
该吸收剂量明显低于先前的估计,允许FDOPA注射剂量高达333兆贝可(9毫居里)。