Jarløv A E, Hegedüs L, Kristensen L O, Nygaard B, Hansen J M
Department of Internal Medicine and Endocrinology F and Ultrasound, Herlev Hospital, Denmark.
Clin Endocrinol (Oxf). 1995 Sep;43(3):325-9. doi: 10.1111/j.1365-2265.1995.tb02039.x.
The persistent controversy as to the best approach to radioiodine dose selection in the treatment of hyperthyroidism led us to perform a study in order to compare a fixed dose regime comprising doses of 185 370 or 555 MBq based on gland size assessment by palpation only, with a calculated 131I dose based on type of thyroid gland (diffuse, multinodular, solitary adenoma), an accurate thyroid volume measurement, and a 24-hour 131I uptake determination.
Prospective randomized study.
Two hundred and twenty-one consecutive hyperthyroid patients referred for 131I treatment. Four Patients who died for reasons unrelated to hyperthyroidism, 7 lost to follow-up and 47 who did not receive antithyroid drugs after treatment, were excluded. The remaining 163 patients (143 women) were studied, divided into subgroups according to the type of gland. They all received antithyroid drugs prior to 131I treatment and this was resumed 7 days after treatment for a period of 3 weeks.
Thyroid function variables were determined approximately 2 weeks before 131I treatment, and again 1, 2, 3, 6, 9 and 12 months after treatment. Prior to 131I therapy the size of the thyroid gland was determined by ultrasound and a 24-hour uptake of 131I was carried out. Thyroid volume was also estimated 12 months after 131I therapy in 78 of the 163 patients. Twelve months after the initial 131I dose patients could be classified as euthyroid, hyperthyroid or hypothyroid.
Neither in the group of 163 patients nor within the three subgroups of hyperthyroidism could any significant difference in outcome between the two treatment regimes be demonstrated. Thirty-two of 78 patients (41%) in the calculated dose group and 30 of 85 patients (35%, NS) in the fixed group were classified as hyperthyroid. Seven of 78 (9%) in the calculated dose group and 6 out of 85 (7%, NS) in the fixed dose group were classified as permanently hypothyroid. Finally, 39 of 78 (50%) in the calculated dose group and 49 of 85 (58%, NS) in the fixed group were euthyroid at 12 months after 131I treatment. One year after 131I therapy thyroid volume was reduced from 59.3 +/- 9.2 (mean +/- SEM) to 36.2 +/- 6.6 ml (average reduction 39%) in the calculated dose group (P < 0.001). This reduction did not differ significantly from the fixed dose group where thyroid volume declined from 61.6 +/- 6.1 to 41.17 +/- 4.7 ml (average reduction 32%) (P < 0.001).
A semiquantitative approach is probably as good as the more elaborately calculated radioiodine dose for treatment of hyperthyroidism. It is clearly more cost effective and allows the use of predetermined standard doses.
关于甲状腺功能亢进症治疗中放射性碘剂量选择的最佳方法一直存在争议,这促使我们开展一项研究,以比较仅基于触诊评估腺体大小的固定剂量方案(分别为185、370或555MBq)与根据甲状腺类型(弥漫性、多结节性、孤立性腺瘤)、准确的甲状腺体积测量以及24小时碘-131摄取测定计算得出的碘-131剂量。
前瞻性随机研究。
连续221例因碘-131治疗前来就诊的甲状腺功能亢进症患者。排除4例因与甲状腺功能亢进症无关的原因死亡的患者、7例失访患者以及47例治疗后未接受抗甲状腺药物治疗的患者。对其余163例患者(143例女性)进行研究,根据腺体类型分为亚组。所有患者在碘-131治疗前均接受抗甲状腺药物治疗,并在治疗7天后重新开始服用3周。
在碘-131治疗前约2周以及治疗后1、2、3、6、9和12个月测定甲状腺功能变量。在碘-131治疗前通过超声确定甲状腺大小并进行24小时碘-131摄取测定。163例患者中的78例在碘-131治疗12个月后还进行了甲状腺体积估计。初始碘-131剂量治疗12个月后,患者可分为甲状腺功能正常、甲状腺功能亢进或甲状腺功能减退。
在163例患者组以及甲状腺功能亢进症的三个亚组中,均未显示两种治疗方案在结局上有任何显著差异。计算剂量组78例患者中有32例(41%)被分类为甲状腺功能亢进,固定剂量组85例患者中有30例(35%,无显著差异)被分类为甲状腺功能亢进。计算剂量组78例中有7例(9%)被分类为永久性甲状腺功能减退,固定剂量组85例中有6例(7%,无显著差异)被分类为永久性甲状腺功能减退。最后,计算剂量组78例中有39例(50%)在碘-131治疗12个月后甲状腺功能正常,固定剂量组85例中有49例(58%,无显著差异)甲状腺功能正常。碘-131治疗1年后,计算剂量组甲状腺体积从59.3±9.2(均值±标准误)降至36.2±6.6ml(平均减少39%)(P<0.001)。该减少与固定剂量组无显著差异,固定剂量组甲状腺体积从61.6±6.1降至41.17±4.7ml(平均减少32%)(P<0.001)。
对于甲状腺功能亢进症的治疗,半定量方法可能与更精细计算的放射性碘剂量一样有效。它显然更具成本效益,并允许使用预定的标准剂量。