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Kaku igaku. The Japanese journal of nuclear medicine最新文献

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[The 47th Report on Survey of the Adverse Reaction to Radiopharmaceuticals (The 50th Survey in 2024)]. 第47次放射性药品不良反应调查报告(2024年第50次调查)。
Pub Date : 2026-01-01 DOI: 10.18893/kakuigaku.rp.2631
Hidehiko Okazawa, Tomoya Uehara, Daiki Kayano, Ichiei Kuji, Tatsuya Higashi, Mana Yoshimura

This survey was performed in order to investigate the incidence of adverse reactions to radiopharmaceuticals in FY2024 in Japan. It was based on responses to questionnaires sent to nuclear medicine institutions. Replies were obtained from 989 institutions out of 1,176 to which the questionnaire had been sent. A total of 925,315 radiopharmaceutical administrations were reported. Nine cases of adverse reactions were reported. The incidence of adverse reactions per 100,000 cases was 1.0. No case of defective products was reported.

本调查是为了调查日本2024财年放射性药物不良反应的发生率。该报告是根据对核医学机构的问卷调查得出的。在收到调查表的1 176个机构中,有989个机构作出了答复。共报告了925,315次放射性药物管理。报告不良反应9例。不良反应发生率为1.0 / 10万例。无不良产品报告。
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引用次数: 0
[Evaluation of Appropriate Treatment Infrastructure for Radionuclide Therapy Through Discrete Event Simulation]. [通过离散事件模拟评估放射性核素治疗的适当治疗基础设施]。
Pub Date : 2025-01-01 DOI: 10.18893/kakuigaku.oa.2503
Takashi Mizowaki, Makoto Hosono, Hiroji Uemura, Masatoshi Eto, Mototsugu Oya, Hideaki Miyake, Masafumi Ikeda, Ayako Kanegasaki, Shunsuke Sakuragi, Yuhei Oida, Seigo Kinuya

Purpose: Radionuclide therapy often involve long waiting periods due to limited numbers of radioisotope therapy rooms and special measures rooms, and strict regulations. The purpose of this study was to estimate the waiting period for radionuclide therapy, considering the increased utilization of nuclear medicine and greater demand due to new drugs. The study also examined possible factors that may limit the treatment provision system and investigate appropriate treatment environments that could shorten the waiting period.

Method: We developed a discrete event simulation, using three prefectures as a model, to predict the number of patients with a long waiting period and determine the effectiveness of environmental measures designed to shorten the waiting period. The model took considered the demand for radionuclide therapy and medical resources, such as the number of treatment beds, as input values.

Results: The simulation predicted that, within 4 years after the introduction of [177Lu]Lu-PSMA-617, the number of patients waiting >180 days for treatment would increase significantly in all three prefectures. The limited number of beds was the leading cause of the long waiting period. However, just increasing the number of beds was ineffective for reducing the waiting period in some facilities due to regulatory factors, and measures to improve the drainage capacity were also necessary.

Conclusion: The number of patients with a long waiting period is expected to increase significantly due to the rapid increase in demand for radionuclide therapy. A combination of measures, including increasing the number of beds, improving drainage capacity, and better utilization of available medical resources through interfacility cooperation, are factors that need urgent attention to reduce the waiting time for radionuclide therapy.

目的:由于放射性同位素治疗室和特殊措施室的数量有限,以及严格的规定,放射性核素治疗往往需要很长的等待期。考虑到核医学利用的增加和新药物的需求增加,本研究的目的是估计放射性核素治疗的等待期。该研究还审查了可能限制治疗提供系统的可能因素,并调查了可以缩短等待期的适当治疗环境。方法:我们开发了一个离散事件模拟,以三个县为模型,预测长等待期的患者数量,并确定旨在缩短等待期的环境措施的有效性。该模型考虑了对放射性核素治疗的需求和医疗资源(如治疗床位数量)作为输入值。结果:模拟预测,在引入[177Lu]Lu-PSMA-617后的4年内,三个县等待治疗的患者数量将显著增加。床位数量有限是等待时间过长的主要原因。但部分设施由于监管因素,单纯增加床位对缩短轮候期效果不明显,还需采取措施提高排水能力。结论:由于放射性核素治疗需求的快速增长,等待期较长的患者数量预计将显著增加。增加病床数量、提高引流能力和通过设施间合作更好地利用现有医疗资源等一系列措施是迫切需要关注的因素,以减少等待放射性核素治疗的时间。
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引用次数: 0
[The 46th Report on Survey of the Adverse Reaction to Radiopharmaceuticals (The 49th Survey in 2023)]. [第46次放射性药品不良反应调查报告(2023年第49次)]。
Pub Date : 2025-01-01 DOI: 10.18893/kakuigaku.rp.2531
Hidehiko Okazawa, Tomoya Uehara, Daiki Kayano, Ichiei Kuji, Tatsuya Higashi, Mana Yoshimura

This survey was performed in order to investigate the incidence of adverse reactions to radiopharmaceuticals in FY2023 in Japan. It was based on responses to questionnaires sent to nuclear medicine institutions. Replies were obtained from 971 institutions out of 1,181 to which the questionnaire had been sent. A total of 884,272 radiopharmaceutical administrations were reported. Fifteen cases of adverse reactions were reported. The incidence of adverse reactions per 100,000 cases was 1.7. No case of defective products was reported.

本调查是为了调查2023财年日本放射性药物不良反应的发生率。该报告是根据对核医学机构的问卷调查得出的。在收到调查表的1 181个机构中,有971个机构作出了答复。报告的放射性药物管理个案共884,272宗。报告不良反应15例。不良反应发生率为1.7 / 10万例。无不良产品报告。
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引用次数: 0
[Special Program Abstracts]. [专题节目摘要]。
Pub Date : 2025-01-01 DOI: 10.18893/kakuigaku.62.S99
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引用次数: 0
Pub Date : 2025-01-01 DOI: 10.18893/kakuigaku.arm.2535
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引用次数: 0
Pub Date : 2025-01-01 DOI: 10.18893/kakuigaku.rgr.2532
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引用次数: 0
Pub Date : 2025-01-01 DOI: 10.18893/kakuigaku.arm.2534
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引用次数: 0
Pub Date : 2025-01-01 DOI: 10.18893/kakuigaku.arm.2533
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引用次数: 0
Pub Date : 2025-01-01 DOI: 10.18893/kakuigaku.62.A6
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引用次数: 0
Pub Date : 2025-01-01 DOI: 10.18893/kakuigaku.62.A1
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引用次数: 0
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Kaku igaku. The Japanese journal of nuclear medicine
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