Venencia Carlos D, Germanier Alejandro G, Bustos Silvia R, Giovannini Andrea A, Wyse Eduardo P
Department of Physics, Instituto Privado de Radioterapia, Córdoba, Argentina.
J Nucl Med. 2002 Jan;43(1):61-5.
A dose limit-based criterion was proposed to authorize hospital discharge of thyroid carcinoma patients treated with 131I. Evaluation of accumulated doses to determine the effective half-life, the expected accumulated dose at 1 m, and the hospitalization time was performed to ensure that the dose limit was satisfied for each patient. Situations involving different dose limits and occupancy factors were analyzed. This study dealt only with external exposure; the problem of internal contamination was not considered.
Fourteen patients treated postoperatively with 131I were studied. The range of activity was 1,110-8,175 MBq. Electronic dosimeters and thermoluminescent dosimeter chips were placed on the left pectoral muscle. Dose was measured for a mean of approximately 2.5 d. The accumulated doses were plotted as a function of time and then fitted using an exponential model to obtain the parameters of total accumulated dose and effective half-life. The doses to the public and relatives at 1 m were calculated with point source approximation and several occupancy factors.
The fit function parameters of accumulated doses in the first 36 h predicted the behavior of the total accumulated dose within a 5% error in the parameters. Estimated values of the accumulated dose 1 m from the patient were generally <5 mSv, even for an occupancy factor of 100%. For more restrictive dose constraints, hospitalization times were calculated according to different occupancy factors, as suggested in the European Commission guide. From the fit of the measured data, values of effective half-life for each patient were obtained.
To apply the dose limit-based criterion, one must calculate the patient-specific parameters, as can be done using the accumulated dose. Knowledge of patient-specific parameters ensures that the patient will not expose any individual to levels greater than the dose limit. The calculated hospitalization times were less than those recommended, especially for countries with more restrictive dose limits. The type of measurements performed in this study reveals more realistic doses for the treatment of thyroid carcinoma with 131I.
提出了一种基于剂量限制的标准,以批准接受131I治疗的甲状腺癌患者出院。进行累积剂量评估以确定有效半衰期、1米处的预期累积剂量以及住院时间,以确保每个患者都符合剂量限制。分析了涉及不同剂量限制和居留因子的情况。本研究仅涉及外照射;未考虑内污染问题。
对14例接受131I术后治疗的患者进行研究。活度范围为1110 - 8175MBq。将电子剂量计和热释光剂量计芯片置于左胸肌处。测量剂量约2.5天。将累积剂量绘制成时间的函数,然后使用指数模型进行拟合,以获得总累积剂量和有效半衰期的参数。使用点源近似和几个居留因子计算1米处公众和亲属所受的剂量。
前36小时累积剂量的拟合函数参数预测总累积剂量的行为时,参数误差在5%以内。即使居留因子为100%,患者1米处累积剂量的估计值通常也<5mSv。对于更严格的剂量限制,根据欧盟委员会指南的建议,根据不同的居留因子计算住院时间。通过对测量数据的拟合,获得了每个患者的有效半衰期值。
要应用基于剂量限制的标准,必须计算患者特定参数,这可以通过累积剂量来完成。了解患者特定参数可确保患者不会使任何个体暴露于超过剂量限制的水平。计算出的住院时间比建议的时间短,特别是对于剂量限制更严格的国家。本研究中进行的测量类型揭示了131I治疗甲状腺癌更实际的剂量。