• 제목/요약/키워드: Lifetime effective dose

검색결과 16건 처리시간 0.02초

An External Dose Assessment of Worker during RadWaste Treatment Facility Decommissioning

  • Chae, San;Park, Seungkook;Park, Jinho;Min, Sujung;Kim, Jongjin;Lee, Jinwoo
    • Journal of Radiation Protection and Research
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    • 제45권2호
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    • pp.81-87
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    • 2020
  • Background: Kori unit #1 is permanently shut down after a 40-year lifetime. The Nuclear Safety and Security Commission recommends establishing initial decommissioning plans for all nuclear and radwaste treatment facilities. Therefore, the Korea Atomic Energy Research Institute (KAERI) must establish an initial and final decommissioning plan for radwaste-treatment facilities. Radiation safety assessment, which constitutes one chapter of the decommissioning plan, is important for establishing a decommissioning schedule, a strategy, and cost. It is also a critical issue for the government and public to understand. Materials and Methods: This study provides a method for assessing external radiation dose to workers during decommissioning. An external dose is calculated following each exposure scenario, decommissioning strategy, and working schedule. In this study, exposure dose is evaluated using the deterministic method. Physical characterization of the facility is obtained by both direct measurement and analysis of the drawings, and radiological characterization is analyzed using the annual report of KAERI, which measures the ambient dose every month. Results and Discussion: External doses are calculated at each stage of a decommissioning strategy and found to increase with each successive stage. The maximum external dose was evaluated to be 397.06 man-mSv when working in liquid-waste storage. To satisfy the regulations, working period and manpower must be managed. In this study, average and cumulative exposure doses were calculated for three cases, and the average exposure dose was found to be about 17 mSv/yr in all the cases. Conclusion: For the three cases presented, the average exposure dose is well below the annual maximum effective dose restriction imposed by the international and domestic regulations. Working period and manpower greatly affect the cost and entire decommissioning plan; hence, the chosen option must take account of these factors with due consideration of worker safety.

소아(10세) 흉부 방사선촬영에서의 두경부 방사선 방어기구 개발 및 평가 (The Evaluation and Development of Head and Neck Radiation Protective Device for Chest Radiography in 10 Years Children)

  • 이준호;임현수;이승열
    • Journal of Radiation Protection and Research
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    • 제40권2호
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    • pp.118-123
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    • 2015
  • 최근 의료기관에서의 진단방사선검사 빈도는 2011년 2억 2천만건, 연간 일인당 피폭선량은 1.4 mSv로 2007년 대비 각 51%, 35% 증가하였다. 여기서 흉부촬영건수는 일반촬영 중 가장 높은 빈도인 27.59%로 나타났다. 따라서 본 연구에서는 흉부 방사선 촬영 시 영상판독에 불필요한 신체부위를 차폐하여 피폭선량을 최소화 시키는 차폐기구를 개발하고, 그 유용성 평가를 위해 국제 표준 소아(10세) 팬텀과 유리선량계를 사용하여 기구 사용 전, 후의 입사표면선량(entrance surface dose; ESD)과 장기의 흡수선량 차를 측정하였다. 또한 몬테카를로 시뮬레이션 기반 프로그램(PCXMC 2.0.1)을 이용하여 유효선량을 산출하였고 암발생의 생애귀속위험도(lifetime attributable risk of cancer incidence; LAR)를 비교하여 그 감소율을 간접적으로 평가하였다. 방어기구를 사용할 때, 입사표면선량(감소율)은 비강 $0.55{\mu}Sv$ (74.06%), 갑상선 $1.43{\mu}Sv$ (95.15%), 식도 $6.35{\mu}Sv$ (78.42%)로 평균 86.36% 감소되었고, 심부선량(감소율)은 경추 $1.23{\mu}Sv$ (89.73%), 침샘 $0.5{\mu}Sv$ (92.31%), 식도 $3.85{\mu}Sv$ (59.39%), 갑상선 $2.02{\mu}Sv$ (73.53%) 흉추 $5.68{\mu}Sv$ (54.01%) 로 평균 72.30%로 감소되어 차폐기구의 유용성을 확인할 수 있었다. 또한, 유효선량은 착용 전 $8.33{\mu}Sv$에서 착용 후 $7.35{\mu}Sv$로 11.76% 감소하였고, LAR 평가에서는 갑상선 암은 10세 소아 백만 명당 남아 0.14명(95.12%), 여아 0.77명(95.16%), 모든 암은 남아 0.14명(11.70%), 여아 0.25명(11.70%)의 감소(감소율)를 확인할 수 있었다. 진단방사선검사는 질병과 치료 등 건강을 위해 꼭 필요한 검사이지만, 가능한 진단에 불필요한 부위에 이러한 차폐기구를 적극적으로 사용하여 ALARA 개념에 입각한 의료방사선 최적화를 도모해야 할 것이다.

Radiometric examination of fertilizers and assessment of their health hazards, commonly used in Pakistan

  • Hannan Younis;Sumbilah Shafique;Zahida Ehsan;Aleena Ishfaq;Khurram Mehboob;Muhammad Ajaz;Abdullah Hidayat;Wazir Muhammad
    • Nuclear Engineering and Technology
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    • 제55권7호
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    • pp.2447-2453
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    • 2023
  • The radioactivity concentrations of Naturally Occurring Radioactive Materials (NORM) i.e., 226Ra, 232Th, and 4K in various chemical fertilizers being used in the agricultural soil of Pakistan were determined utilizing gamma spectrometry by employing a High Purity Germanium (HPGe) detector. The radioactivity concentrations of 226Ra, 232Th, and 4K extended from 2.58 ± 0.8-265.7 ± 8.8 Bq kg-1, 1.53 ± 0.14-76.6 ± 1.07 Bq kg-1 and 36.5 ± 1.34-15606.7 ± 30.2 Bq kg-1 respectively. The radiological hazard parameters such as internal and external indices and annual effective dose rates were calculated, while excessive lifetime cancer risk factors for the indoor and outdoor areas were found in the range from 0.3×10-3 to 10.723×10-3 and 0.03×10-3 to 2.7948×10-3 of most fertilizers, however, some values were slightly higher than the UNSCEAR (The United Nations Scientific Committee on the Effects of Atomic Radiation) recommended values for potash-containing fertilizers such as MOP (Muriate of Potash).

Feasibility Assessment of Physical Factors of Rectal Cancer Short-Course Chemoradiotherapy with Delayed Surgery

  • Koo, Jihye;Chung, Mijoo;Chung, Weon Kuu;Jin, Sunsik;Kim, Dong Wook
    • 한국의학물리학회지:의학물리
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    • 제29권4호
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    • pp.143-149
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    • 2018
  • To verify the correlations between the clinical outcomes and physical factors of short-course chemoradiotherapy (SCRT) and long-course chemoradiotherapy (LCRT) with delayed surgery in patients with rectal cancer. Seventy-two patients with rectal cancer were enrolled in this study. Nineteen patients were treated with SCRT (25 Gy, 5 fractions) by intensity-modulated radiation therapy (IMRT), and 53 patients were treated with LCRT (50.4 Gy, 28 fractions) by three-dimensional conformal radiation therapy (3DCRT). Various physical factors for the target and organs at risk (OARs) were calculated to compare the clinical outcomes. The organ equivalent dose (OED) and lifetime attributable risk (LAR) of bowels and bladders were similar between the SCRT and LCRT groups, whereas the values of femurs were higher in the LCRT group. The equivalent uniform dose and normal tissue complication probability were higher in the LCRT than the SCRT group for most organs. Treatment complications, including anastomotic leakage, bowel adhesion, and hematologic toxicity, were not significantly different between SCRT and LCRT groups. CIs were $0.84{\pm}0.2$ and $0.61{\pm}0.1$ for SCRT and LCRT, respectively. The CVIs were $1.07{\pm}0.0$ and $1.10{\pm}0.1$, and the HIs were $0.09{\pm}0.0$ and $0.11{\pm}0.1$ for SCRT and LCRT, respectively. The sphincter-saving rates were 89.5% and 94.3% for SCRT and LCRT, respectively. The complete pathologic remission rates were 21.1% and 13.2%, and the down-staging rates were 47.4% and 26.4% for SCRT and LCRT, respectively. SCRT with IMRT is comparable to conventional LCRT in both physical indexes and clinical outcome. The preoperative SCRT, compensated by IMRT, is an effective and safe modality.

암의 조기발견을 위한 CT촬영에서의 임상적 효능과 방사선위해에 대한 고찰 (Review of the Radiation Risk and Clinical Efficacy Associated with Computed Tomography Cancer Screening)

  • 김현자
    • Journal of Radiation Protection and Research
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    • 제38권4호
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    • pp.214-227
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    • 2013
  • MDCT의 등장과 함께 병적 증상이 없는 개인이 조기검진을 위해 CT검사를 하는 예가 꾸준히 증가하고 있다. 이러한 검사의 임상적 효용성과 방사선에 의한 암 발생위험에 대한 여러 가지 논란을 살펴보았다. 1. 저선량흉부CT(LDCT)를 이용한 폐암의 조기 검진 효용성을 보기 위해 설계된 무작위배정대조검사(randomized controlled trial)인 NLST(National Lung Screening Trial)의 분석 결과, CT선별검사가 선별검사를 하지 않은 그룹의 사망률 1.67%를 1.33%로, 20% (p=0.004) 감소시키는 것으로 나타났다. CT선별검사군에서 양성결과를 보인 사람의 96.4%는 위양성(false-positive)이었다. 그리고 방사선에 의한 폐암의 ERR (excess radiation risk)은 다른 고형암과는 달리 나이와 함께 감소하지 않으며, 더욱이 흡연 위험과 방사선 위험이 상승작용을 하여 폐암 검진 대상인 고위험군에게 더욱 위험할 수 있는 것으로 평가되었다. 따라서 방사선에 의한 위험이 NLST에서 관측한 이득을 상쇄할 수도 있다. 아직은 최적의 전략이 확립되지 않은 상태이므로 임상에서 광범위하게 적용하기에는 한계가 있다. 2. 대장CT검사(CT colonography)는 10 mm보다 큰 용종의 검출에는 정확도가 뛰어나지만 이보다 작은 경우에는 민감도와 특이도가 급격히 감소하고, 용종이 발견되어 제거하고자 하는 경우 다시 기존의 대장내시경을 이용해야 하는 불편함이 있다. 현재 대장CT검사 1회 시행의 평균유효선량은 약 8-10 $mS{\nu}$로 보고되어, 만약 이 검사가 많은 사람들을 대상으로 일상적으로 행해지면 공중보건에 영향을 미칠 수 있다. 따라서 집단검진 방법으로 정착하기 위해서 는 용종 크기 6-10 mm 범위에서 높은 민감도와 특이도를 확립하고, 하제를 사용하지 않는 방법을 개발하여야 하며, 선량을 더 감소시킬 수 있는 최적화된 전략을 세워 표준화하여야만 한다. 3. 전신CT검사는 그 효용성이 검증된 선행연구가 없는 상태이다. 이 검사는 약 90%의 검사자들에게서 최소한 하나 이상의 이상소견을 확인하였지만 그 중 약 2%만이 임상적으로 중요한 질환으로 판명되었다. 전신CT검사 1회 시행으로 인한 평균유효선량은 약 12 $mS{\nu}$이며 45세부터 75세까지 매년 검사를 받는 경우 LAR (lifetime attributable risk)이 1.9%로 보고되었다. 현재 의학계의 어떤 단체도 이 검사를 권고하고 있지 않다. 현재까지 CT선별검사는 정당화에 대한 충분한 논의를 위해 심도 있는 다양한 연구가 필요하며 최적화된 프로토콜이 확립된 후 이용하는 것이 바람직하다.

인후두역류의 약물치료 (Medical Treatment of Laryngopharyngeal Reflux)

  • 주형로
    • 대한후두음성언어의학회지
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    • 제18권2호
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    • pp.108-112
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    • 2007
  • Otolaryngological manifestations of acid reflux include a wide range of pharyngeal and laryngeal symptoms ; and the constellation of symptoms has been called laryngopharyngeal reflux (LPR). In the absence of definite diagnostic criteria, LPR disease remains a subjective entity. A diagnosis of LPR is usually based on response of symptoms to empirical treatment. Investigative modalities such as pH monitoring and, more recently, impedance studies are generally reserved for treatment failures. LPR usually requires more aggressive and prolonged treatment to achieve regression of both symptoms and laryngeal findings. The suppression of gastric acid and secretion with anti-secretary agents has been the mainstay of medical treatment for patients with acid-related disorders. The suppression of gastric acid secretion achieved with Hz-receptor antagonist $(H_2RA)$ has proved suboptimal for relief of reflux symptoms. The rapid development of tolerance and rebound acid hypersecretion after the with-drawal of $H_2RA$ limit their clinical use. Proton pump inhibitors (PPI) have been proved to be very effective for suppressing intragastric acidity, but the optimal dose and duration is unknown. Current evidence indicates that pharmacologic intervention should include, at a minimum, a 3 month trial of twice daily PPI. Symptoms of LPR improve over 2 months of therapy. The physical findings of LPR resolve more slowly than the symptoms and this continues through out at least 6 months of treatment. For most patients with LPR, twice daily dosing with a PPI is usually recommended for an initial treatment for a period of no less than 6 months treatment, and lifetime treatment may be required.

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