1.Primary care physicians attitudes and practice for management of osteoporosis in Inchon city.
So Jeong LEE ; Young Oh JANG ; Sang Hyun YI ; In Ho KAWK ; Ji Ho CHOI ; Hun Mo YI
Journal of the Korean Academy of Family Medicine 1998;19(6):437-444
No abstract available.
Hormone Replacement Therapy
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Humans
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Incheon*
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Osteoporosis*
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Physicians, Primary Care*
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Primary Health Care*
2.The Significance of Persistent Abnormal Urine Cytology.
Sang Wook PARK ; In Ho CHANG ; June Hyun HAN ; Kyung Won KAWK ; Seung Hyun AHN
Korean Journal of Urology 2009;50(2):125-129
PURPOSE: We investigated the factors that predicted later transitional cell carcinoma (TCC) in a subgroup of patients with abnormal cytology and negative initial evaluations. MATERIALS AND METHODS: From January 2002 to June 2007, we retrospectively identified 58 patients. Cases were considered discordant if a work-up of urine cytology was abnormal although initial cystoscopy, upper tract evaluation, and biopsies resulted in a negative or benign diagnosis. Patients who could complete a urine cytology test after 6 to 8 weeks and who were followed up for at least 1 year were included in this study. According to later TCC demonstration, we compared risk factors for TCC between the later TCC group and the benign group and evaluated the independent factors that predicted later TCC by use of a Cox proportional hazards regression model. RESULTS: Of the 58 patients, the mean follow-up was 12.7+/-17.3 months (range: 2-83 months), and 14 patients (23.7%) had a prior history of TCC. During follow-up, 9 patients (15.3%) had TCC and 1 patient had prostate cancer. In the later TCC group, the incidence of a prior history of TCC (p=0.03) and persistent abnormal cytology (p<0.001) were higher than in the benign group in univariate analysis. In the Cox proportional hazards regression model, persistent abnormal cytology (p=0.033, relative risk (RR): 17.380 [95% CI: 1.265-238.783]) was the only independent factor to predict later TCC. The mean follow-up duration of later TCC demonstration was 8.55 months (range: 2-32 months). CONCLUSIONS: Our results suggest that in the setting of persistent abnormal urine cytology with a negative initial evaluation, 53.3% of patients will later develop TCC. Patients with persistent abnormal cytology need intensive follow-up within 1 year.
Biopsy
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Carcinoma, Transitional Cell
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Cystoscopy
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Follow-Up Studies
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Humans
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Incidence
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Prostatic Neoplasms
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Retrospective Studies
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Risk Factors
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Urinary Bladder
3.The Change of Cognitive Function and Prognostic Factor in Alzheimer's Disease: 1-Year Follow-up Study.
Tae You KIM ; Sang Yun KIM ; Tae Yong HONG ; Sang Min SUNG ; Sung Min YOON ; Eun Ah LEE ; Kang Ho KAWK ; Yon Kwon IHN
Journal of the Korean Neurological Association 2005;23(1):21-27
BACKGROUND: The rate of cognitive change and prognostic factor in Alzheimer's disease are important for clinical management, but little is known in Korea. We report a one year follow-up study of comprehensive evaluation including cognitive functions, behavioral and psychological symptoms of dementia (BPSD) and activity of daily living (ADL). METHODS: 43 patients with Alzheimer's disease were enrolled. All subjects received the Korean version of Mini-Mental State Examination (K-MMSE), the Severe Dementia Scale (SDS), the extended version of Korean Clinical Dementia Rating Scale (CDR) and Sum of Box (CDR-SB), the Barthel index of Activity of Daily Living (B-ADL), the Korean Instrumental Activity of Daily Living (K-IADL) and the Korean version of the Neuropsychiatric Inventory (K-NPI). We retested each scale after 1 year and evaluated the changes. RESULTS: The mean change rates of K-MMSE, SDS, CDR, CDR-SB and B-ADL scores were 2.0 +/- 3.2 (-7~8) mean +/- SD (range), 3.5 +/- 4.9 (-7~14), -0.4 +/- 0.7 (-2~1), -0.8 +/- 4.4 (-10~9) and 1.5 +/- 3.7 (-7~9). The change of K-MMSE and B-ADLscore according to CDR were significantly different. The annual rates of changes of scores on K-MMSE, B-ADL and CDR were largest in CDR 1 group (K-MMSE: 4.0 +/- 2.7, B-ADL: 3.4 +/- 2.8, CDR: -1 +/- 0.7). The change rate of SDS was largest in CDR 4 (7.2 +/- 4.3). There were not any significant factors that affected the change of K-MMSE, SDS, B-ADL or CDR. CONCLUSIONS: These results suggest that K-MMSE is sensitive to the early stage and SDS is sensitive to the later stage. The deterioration rate of cognitive function in Alzheimer's disease is large at middle stage.
Alzheimer Disease*
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Cognition
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Dementia
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Follow-Up Studies*
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Humans
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Korea
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Longitudinal Studies
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Prognosis