• 생물정신의학
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• 제18권1호
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• pp.36-45
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• 2011

Objectives : Though a proportion of Alzheimer's disease(AD) patients treated with donepezil have shown positive response on cognition, but the responders' characteristics are still uncertain. This study attempts to identify whether a single oral dose of donepezil(5mg) can change cognition and the relationship between single dose responder items and long-term responder are examined. Methods : Twenty-three AD patients for single donepezil challenge study group and eleven AD patients for controls were participated in the study. Seven days after baseline study for neuropsychological test and EEG, same studies were rechecked after donepezil medication in study group. In donepezil study groups, 12 weeks after donepezil medication, neuropsychological test and EEG were rechecked. Results : After single donepezil challenge, forward digit span, Rey-Osterrieth Complex Figure Test copy, SVLT delayed recall were significantly improved, and beta spectra power in anterior, theta spectra power in posterior field were significantly decreased. According to linear regression analysis, forward digit span after single donepezil challenge was significantly positive correlated with long-term responders. Conclusions : This study suggests that single donepezil medication can significantly change cognitive functions and EEG in AD patients. Among these responsive items, forward digit span was significantly correlated with long-term responder.

• Radiation Oncology Journal
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• 제7권2호
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• pp.259-267
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• 1989

Forty one patients with para-aortic node metastases from carcinoma of the uterine cervix treated with radiotherapy at Department of Radiation Oncology, Yonsei University, College of Medicine from January 1982 to December 1987 were retrospectively analyzed. Eleven patients were diagnosed at the time of diagnosis of carcinoma of the cervix (early diagnosis) and 30 patients were diagnosed during follow up period after definitive radiotherapy of primary site (late diagnosis). The most important factors affecting the survival in this study were time of diagnosis and dose of irradiation. Overall 5 year actuarial survival rate of 41 patients was $25.7\%$. Five year survival rate for early diagnosis was $60.3\%$, but late diagnosis was $16.9\%$. And survival rate for high dose (over 4000 cGy) radiation group and low dose radiation group were $42.2\%\;and\;8.9\%$ respectively The most leading cause of death was para-aortic node failure, so early diagnosis and maximum palliation with full dose radiotherapy (over 4000 cGy) is necessary to improve the survival and the quality of life.

• 대한방사선기술학회지:방사선기술과학
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• 제34권3호
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• pp.209-214
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• 2011

TACE의 중재적 시술시 환자와 시술자가 받는 피폭선량을 평가하고, 환자의 피폭선량을 최소화하기 위한 방안을 모색하기 위함이다. 2010년 6월부터 9월까지 중재적 시술의 빈도와 방사선 피폭의 양이 비교적 큰 TACE 시술환자를 대상으로 혈관조영장비(Philips Allura Xper FD 20)와 장비내 장착된 Ionization chamber에 의해 나타나는 DAP(Dose area product)값에 교정상수를 적용시켜 시술시 환자가 받는 유효선량을 근사적으로 얻어냈으며 환자와 시술자의 갑상선과 생식선 주위에 TLD를 부착하여 피폭선량을 산출하고 SPSS 통계에 의한 분석과 평가를 하였다. DAP값에 의해 산출된 TACE 시술시 1인당 ED(Effective Dose)는 평균 18.43${\pm}$6.63 mSv로 나타났으며 이는 전국 평균값의 75%에 해당한다. 또한 TLD에 의해 측정된 환자의 갑상선과 생식선부위의 1인당 평균피폭선량은 각각 0.37 mSv, 0.77 mSv로 나타났으며 보호용구를 착용한 시술자는 환자 1인당 각각 0.07 mSv, 0.01 mSv의 평균피폭선량을 받았다. 시술에 참여하는 모든 의료진들은 법적 선량한도의 적용을 받지 않는 방사선의료피폭에 대해 경각심을 가져야하며, 영상모니터에 실시간으로 표시되는 DAP값을 이용하여 환자의 피폭선량을 고려하며 시술에 임해야하며 시술에 방해가 되지 않는 한도 내에서 환자에게 차폐용구를 적절히 활용해야 한다.

• Radiation Oncology Journal
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• 제13권4호
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• pp.339-348
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• 1995

목적 : 위암의 간문맥 임파절 재발로 발생한 악성 폐쇄성 황달치료에 있어서 외부 방사선치료의 효과를 평가해 보고 치료의 결과에 영향을 미칠 수 있는 요인을 알아보고자 하였다. 방법 : 1984년부터 1993년까지 위암의 간문맥 전이로 악성 폐쇄성 황달이 발생한 32명중 3000cGy이상의 방사선량이 조사된 23명을 대상으로 하였다. 치료 결과에 영향을 미칠 수 있는 요인을 알아보기 위하여 방사선량, 황달발생 당시의 질병의 진전정도 및 황달을 일으키는 종피의 위치, 방사선치료 전 총 bilirubin치, 다른 치료와의 병합여부, 원발병소의 수술정도, 재발전 병기를 분석하였다. 외부 방사선치료는 4백만 전자볼트 선형가속기를 이용하여 주 5회, 1회 180-300cGy를 간문맥을 포함하는 부위에 3000cGy-5480cGy(중앙값 3770cGy,TDF 49-86 3420cGy-5580cGy 중앙값 TDF 65, 4140cGy/23fx)가 조사되었다. TDF 65(4140cGy/23fx 이상과 미만을 받은 환자는 각각 13, 10명이었다. 결과 : 전체 환자 23명중 완전관해 13명, 부분관해 5명, 무반응 5명이었다. 전체 환자의 중앙 생존 기간은 5개월이나 완전관해의 경우는 11개월이고 부분관해와 무반응의 경우 각각 3개월이었다. 완전관해를 보인 13명중 6명이 1년 이상 생존하였다. 완전관해의 경우와 부분관해, 무반응과의 생존 기간의 비교에서 의미있는 차이를 보였다(p<0.05). TDF 65인 4140cGy 이상을 받은 13명중 완전관해, 부분관해, 무반응이 각각 10, 2, 1명이었다. 이들 전체환자의 중앙 생존 기간은 9.5개월 이었고 완전관해를 이룬경우 11.5개월 이었다. 그러나 TDF 65(4140cGy/23fx) 미만을 받은 10명중 완전관해, 부분관해, 무반응이 각각 3, 3, 4명 이었고 이들의 중앙 생존 기간은 4.3개월 이었다. 따라서 방사선량이 치료 결과에 영향을 미치며 완전관해를 이루기 위해서는 TOF 65(4140cGy/23fx)이상이 조사되어야 할 것이다. 치료시 질병의 진전정도는 완전관해를 보인 경우 7명이 간문맥이나 췌장 주위에만 국한된 병변을가졌고(5명 담도계하부 병변) 무반응과 부분반응을 보인 모든 환자는 광범위한 질병의 진전이 있거나, 일차병변의 지속상태였다. 질병의 진전상태가 국소적일수록, 담도계하부에 국한되어 있을수록 완전관해의 가능성이 높고 1년 이상 장기생존이 가능할 것으로 추정된다. 완전관해인 경우 10명이 방사선치료후 계속적인 항암화학요법을 받았고 이들중 6명이 1년 이상 생존하였다. 치료 결과에 영향을 미칠 것으로 추정되는 요인으로 방사선량, 황달 발생당시 질병의 진전정도 및 황달을 일으키는 종괴의 위치로 분석 되었다. 외부 방사선치료중 경미한 위장관 부작용(오심, 구토)이 발생하였으나 방사선치료 시행에 영향을 미치지 않았다. 결론 : 위암의 재발로 인해 발생한 악성 폐쇄성 황달환자의 치료에 있어서 TDF 65(4140cGy/23fx) 이상의 외부 방사선치료 단독으로도 만족할 만한 고식적 효과를 이룰수 있고 방사선량과 재발 당시 질병의 진전정도가 치료 결과에 영향을 미칠 수 있는 요인으로 생각 된다.

• Journal of Trauma and Injury
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• 제26권3호
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• pp.198-206
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• 2013

Purpose: This study was performed to calculate and analyze the effective radiation doses from computed tomography (CT) and radiologic intervention in patients in the emergency department (ED) with trauma critical pathway (CP) activation and further to estimate the lifetime attributable risks (LARs) for the incidence of and mortality from cancers induced by the radiation dose. Methods: Through a retrospective electrical chart review of 104 injured patients who trauma critical pathway were activated from November 2012 to March 2013, we calculated effective radiologic doses by taking the product of the dose-linear product of the scan and the conversion coefficient. After a determination of the image results, we divided the patients into two groups, negative or positive, and calculated the effective dose for each group. With these results, we estimated the LARs for the incidence of and the mortality from cancers by using the table in the Biologic Effects of Ionizing Radiation (BEIR)-VII report. Results: A total of 76 patients were enrolled. The mean age was $49.0{\pm}8.5$ years. The mean injury severity score (ISS) was $12.7{\pm}8.4$. The cumulative effective dose (CED) for individual patients varied from 2.8 mSv to 238.8 mSv, and the mean was $47.6{\pm}39.9$ mSv. The CED in patients with an $ISS{\geq}16$($63.2{\pm}26.6$ mSv) was higher than that of patients whose ISS<16($33.5{\pm}23.1$ mSv) (p<0.001). The CED in patients who were treated with surgery or intervention($69.0{\pm}45.2$ mSv) was higher than that of patients who were treated conservatively($33.6{\pm}22.4$ mSv) (p<0.001). The LARs for cancer incidence and mortality were $328.5{\pm}308.6$ and $189.0{\pm}159.3$ per 100,000 people, respectively. Conclusion: The CED and the LAR for trauma CP-activated patients in the ED were significant, so efforts should be made to decrease the effective dose received by severely injured patients.

• 대한약침학회지
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• 제22권3호
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• pp.171-175
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• 2019

Objectives: TA is a polyherbal extract comprising seven herbs, typically used for the pharmacopuncture treatment of patients with traffic accident- related injuries and musculoskeletal diseases. This animal study was conducted to evaluate the safety of the TA extract, using a single-dose toxicity test. Methods: The dose range and sampling time were first established. Six- week-old Sprague-Dawley rats were administered 1.0 mL of TA or normal saline (control), intramuscularly, for the single-dose toxicity test. The general condition, mortality, and histology of all rats were observed for 2 weeks. Results: No abnormal symptoms or deaths were observed in any group. The body weights of the rats in the TA and control groups were similar. No significant differences in histopathology were observed between the groups. Conclusion : Our study indicates that 1.0 mL of TA extract may be safely administered for pharmacopuncture for treatment of patients in traditional medicine clinics.

• 대한임상독성학회지
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• 제9권2호
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• pp.56-60
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• 2011

Purpose: The optimal dose of oximes for use in the treatment of organophosphorus pesticide poisoning has not been conclusively established. In this retrospective study, we assessed the effectiveness of the use of high-dose pralidoxime infusion in treating organophosphorus pesticide poisoning. Methods: From January 1998 to December 2009, 71 patients visited the hospital Emergency Department (ED) as a result of organophosphate pesticide intoxication. All of these patients received an initial bolus of 2 g of pralidoxime as the first step of treatment. Patients who then received continuous infusion of pralidoxime at a dose of 500 mg/hr were entered into study group 1 (low dose), and those treated by continuous infusion of pralidoxime at a dose of 1000 mg/hr were entered into study group 2 (high-dose). Plasma cholinesterase activities for each patient were evaluated at ED arrival and re-evaluated 24 hours after pralidoxime infusion. The effectiveness of the two treatment modalities was gauged by comparing the required duration of mechanical ventilation, time spent in the intensive care unit (ICU) and total time spent in the hospital. Results: The mean duration of mechanical ventilation was $9.98{\pm}6.47$ days for group 1 and $4.39{\pm}6.44$ days for group 2. The respective mean duration of time spent in ICU and the total number of days in the hospital were $16.38{\pm}18.84$ days and $21.87{\pm}20.16$ days for group 1, and $7.83{\pm}9.99$ days and $11.71{\pm}13.53$ days for group 2. Highdose pralidoxime treatment was associated with shorter required durations for mechanical ventilation, ICU and hospital stay. In addition, plasma cholinesterase reactivation rates were higher for those patients receiving high-dose pralidoxime treatment. Conclusion: The results suggest that high-dose pralidoxime treatment has greater efficacy for patients suffering from organophosphorus pesticide poisoning.

• The Korean Journal of Pain
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• 제14권2호
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• pp.186-192
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• 2001

Background: Epidural test doses containing epinephrine are an incomplete marker for the detection of inadvertent intravascular injection. Therefore, many investigators have attempted to find a more reliable marker as an alternative to epinephrine in adult patients anesthetized with enflurane. The present study was designed to test whether two different simulated intravenous test doses of isoproterenol could be used as a reliable marker for the detection of inadvertent intravascular injection in adult patients anesthetized with $O_2-N_2O$-enflurane. Methods: Forty healthy adult patients were anesthetized with 1% end-tidal enflurane and nitrous oxide after endotracheal intubation and were randomized to one of two groups according to the dose of isoproterenol. Group 1 and 2 (n = 20 each) received 3 ml of 1.5% lidocaine with 3 and 5 g isoproterenol intravenously, respectively, to simulate an intravascularly administered test dose. Heart rate (HR) and systolic blood pressure (SBP) were measured at 20-second intervals for 4 min after injection. Results: Mean maximal HR increases were $24{\pm}17$, $35{\pm}11$ bpm (P < 0.05), mean maximal SBP increases were $14{\pm}8$, $13{\pm}9$ mmHg and mean maximal SBP decreases $20{\pm}11$, $22{\pm}9$ mmHg following the IV injection of 3, $5{\mu}g$ isoproterenol, respectively. The incidence of hypotension was similar in both groups. Isoproterenol 3 and $5{\mu}g$ produced 75%, 100% sensitivity in the HR criteria ($\geq$ 20 bpm increase) and 60%, 70% sensitivity in the SBP criteria ($\geq$ 15 mmHg), respectively. Conclusions: These results indicate that based on the HR response, the epidural test dose containing $5{\mu}g$ isoproterenol to simulate an intravascular administration is a more reliable marker than $3{\mu}g$ isoproterenol in adult healthy patients during enflurane anesthesia.

• Radiation Oncology Journal
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• 제32권4호
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• pp.247-255
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• 2014

Purpose: To determine whether neoadjuvant androgen deprivation therapy (NADT) improves clinical outcomes in patients with prostate cancer treated with definitive radiotherapy. Materials and Methods: We retrospectively reviewed medical records of 201 patients with prostate cancer treated with radiotherapy between January 1991 and December 2008. Of these, 156 patients with more than 3 years of follow-up were the subjects of this study. The median duration of follow-up was 91.2 months. NADT was given in 103 patients (66%) with median duration of 3.3 months (range, 1.0 to 7.7 months). Radiation dose was escalated gradually from 64 Gy to 81 Gy using intensity-modulated radiotherapy technique. Results: Biochemical relapse-free survival (BCRFS) and overall survival (OS) of all patients were 72.6% and 90.7% at 5 years, respectively. BCRFS and OS of NADT group were 79.5% and 89.8% at 5 years and those of radiotherapy alone group were 58.8% and 92.3% at 5 years, respectively. Risk group (p = 0.010) and radiation dose ${\geq}70Gy$ (p = 0.017) affected BCRFS independently. NADT was a significant prognostic factor in univariate analysis, but not in multivariate analysis (p = 0.073). Radiation dose ${\geq}70Gy$ was only an independent factor for OS (p = 0.007; hazard ratio, 0.261; 95% confidence interval, 0.071-0.963). Conclusion: NADT prior to definitive radiotherapy did not result in significant benefit in terms of BCRFS and OS. NADT should not be performed routinely in the era of dose-escalated radiotherapy.

• 대한두경부종양학회지
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• 제14권2호
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• pp.214-219
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• 1998

Objectives: To assess the effectiveness of the low-dose(30mCi) I-131 ablation therapy for remnant thyroid tissue following total thyroidectomy for differentiated thyroid cancer. Methods: Between March 1995 and December 1997, forty-eight patients were given ablative doses(30mCi) of I-131 after total thyroidectomy for differentiated thyroid cancer in the presence of I-131 uptake in remnant thyroid tissue. Effective ablation of remnant thyroid tissue was determined by following I-131 whole body scan. if remnant thyroid tissue remained, we repeated the same management at 6 months interval. Results: Thirty-eight(79.1%) patients had papillary, 8(16.7%) follicular, 1(2.1%) medullary and 1(2.1%) Hurthle cell type cancer. Forty-eight patients underwent total thyroidectomy, among those central neck dissection was performed in 35 cases, and modified radical neck dissection in 14 cases. Postoperative complication developed in 8 cases, which included 4 cases of transient hypoparathyroidism, 1 case of permanent hypoparathyroidism, 2 cases of transient recurrent laryngeal nerve palsy, and 1 case of wound hematoma. There were significant remnant thyroid tissue in 46 cases(95.8%) of patients after total thyroidectomy, which could be ablated by low dose(30mCi) I-131. There were no statistical difference between operative procedures and number of treatment of I-131. Conclusions: These results suggested that repeated low-dose(30mCi) I-131 therapy would be needed, therefore, high -dose I-131 therapy could be considered as ablation therapy for the remnant thyroid tissue after total thyroidectomy for differentiated thyroid cancer.