1.Amphetamine-Like Weight Reduction Drug Induced Acute Cardiomyopathy with Left Ventricular Thrombosis.
Jeong Min KIM ; Sung Kee RYU ; Jae Woong CHOI ; Dong Geum SHIN ; Yung Hee LEE ; Hye Ran KANG ; Won Young CHAE ; Ji Sang PARK
The Ewha Medical Journal 2014;37(Suppl):S37-S40
A 37-year-old female patient admitted due to dyspnea on exertion and peripheral edema. For one and a half years, the patient had been taking various drugs and supplements to reduce weight, including amphetamine-like drugs. The patient had no major cardiovascular risk factors except three pack-years of smoking. A chest computed tomography showed a 1.7 cm diameter, capsulated space-occupying lesion in the left ventricle (LV) and 2-dimensional echocardiography showed LV systolic dysfunction (Left ventricular ejection fraction [LVEF], 30%) with a mobile cystic mass (1.1x1.8 cm) that was attached to the LV apex, which was increased in size and number the next day, even with low dose low-molecular-weight heparin. With an increased dose of anticoagulation medication and heart failure management with diuretics and angiotensin receptor II blocker, LV dysfunction was recovered and the LV thrombus disappeared.
Adult
;
Amphetamine
;
Angiotensins
;
Cardiomyopathies*
;
Diuretics
;
Dyspnea
;
Echocardiography
;
Edema
;
Female
;
Heart Failure
;
Heart Ventricles
;
Heparin, Low-Molecular-Weight
;
Humans
;
Risk Factors
;
Smoke
;
Smoking
;
Stroke Volume
;
Thorax
;
Thrombosis*
;
Weight Loss*
2.Occurrence and characterization of oseltamivir-resistant influenza virus in children between 2007-2008 and 2008-2009 seasons.
Seoung Geun KIM ; Yoon Ha HWANG ; Yung Hae SHIN ; Sung Won KIM ; Woo Sik JUNG ; Sung Mi KIM ; Jae Min OH ; Na Young LEE ; Mun Ju KIM ; Kyung Soon CHO ; Yeon Gyeong PARK ; Sang Kee MIN ; Chang Kyu LEE ; Jun Sub KIM ; Chun KANG ; Joo Yeon LEE ; Man Kyu HUH ; Chang Hoon KIM
Korean Journal of Pediatrics 2013;56(4):165-175
PURPOSE: There was a global increase in the prevalence of oseltamivir-resistant influenza viruses during the 2007-2008 influenza season. This study was conducted to investigate the occurrence and characteristics of oseltamivir-resistant influenza viruses during the 2007-2008 and 2008-2009 influenza seasons among patients who were treated with oseltamivir (group A) and those that did not receive oseltamivir (group B). METHODS: A prospective study was conducted on 321 pediatric patients who were hospitalized because of influenza during the 2007-2008 and 2008-2009 influenza seasons. Drug resistance tests were conducted on influenza viruses isolated from 91 patients. RESULTS: There was no significant difference between the clinical characteristics of groups A and B during both seasons. Influenza A/H1N1, isolated from both groups A and B during the 2007-2008 and 2008-2009 periods, was not resistant to zanamivir. However, phenotypic analysis of the virus revealed a high oseltamivir IC50 range and that H275Y substitution of the neuraminidase (NA) gene and partial variation of the hemagglutinin (HA) gene did not affect its antigenicity to the HA vaccine even though group A had a shorter hospitalization duration and fewer lower respiratory tract complications than group B. In addition, there was no significant difference in the clinical manifestations between oseltamivir-susceptible and oseltamivir-resistant strains of influenza A/H1N1. CONCLUSION: Establishment of guidelines to efficiently treat influenza with oseltamivir, a commonly used drug for treating influenza in Korean pediatric patients, and a treatment strategy with a new therapeutic agent is required.
Child
;
Drug Resistance
;
Hemagglutinins
;
Hospitalization
;
Humans
;
Influenza, Human
;
Inhibitory Concentration 50
;
Neuraminidase
;
Orthomyxoviridae
;
Oseltamivir
;
Prevalence
;
Prospective Studies
;
Respiratory System
;
Seasons
;
Viruses
;
Zanamivir
3.Clinical practice guideline for dementia by Clinical Research Center for Dementia of South Korea.
Bon D KU ; Shin Gyeom KIM ; Jun Young LEE ; Kee Hyung PARK ; Joon Hyun SHIN ; Kwang Ki KIM ; Young Chul YOUN ; Yung Min LEE ; Chang Hyung HONG ; Sang Won SEO ; Duk L NA ; Sung Yoon KIM ; Hae Kwan CHEONG ; Doh Kwan KIM ; Jae Hong LEE ; Sang Yun KIM ; Byeong Kil YEON ; Soo Young KIM ; Seol Heui HAN
Journal of the Korean Medical Association 2011;54(8):861-875
The Clinical Research Center for Dementia of South Korea (CREDOS), a nation-wide clinical dementia research group, has prepared clinical practice guidelines (CPG) for dementia tailored to the Korean population. In this article, a summary of the CREDOS CPG is presented with the Korean and English version of full report included in the appendix. The CREDOS CPG in intended not only for psychiatrists and neurologists, but also internists, family physicians, and other primary care physicians involved in the prevention and early diagnosis of dementia. While our CPG for dementia mainly covers Alzheimer's disease (AD) and vascular dementia (VaD), it also includes mild cognitive impairment (MCI) and vascular MCI, which are currently known to be the preclinical stages of AD or VaD, respectively, with emphasis placed on early diagnosis. The CREDOS CPG aims to achieve the following goals by developing CPG for dementia: to establish evidence-based, objective and clear clinical standards for dementia; to improve the clinical decision-making process for patients with dementia; to provide scientific and systematic scales to aid in the work of dementia specialists; to suggest comprehensive and systematic healthcare services tailored to each dementia subtype. The CREDOS CPG focuses on diagnosis and evaluation of clinical practice available domestically, and provides useful concepts of dementia. Its emphasis is on etiologies and epidemiology, diagnostic criteria and evaluation, neuropsychological tests, behavioral and psychological symptoms, the activities of daily living, laboratory tests, and brain imaging.
Activities of Daily Living
;
Alzheimer Disease
;
Appendix
;
Delivery of Health Care
;
Dementia
;
Dementia, Vascular
;
Early Diagnosis
;
Humans
;
Mild Cognitive Impairment
;
Neuroimaging
;
Neuropsychological Tests
;
Physicians, Family
;
Physicians, Primary Care
;
Psychiatry
;
Republic of Korea
;
Weights and Measures
4.Phase II Study of Low-dose Paclitaxel and Cisplatin as a Second-line Therapy after 5-Fluorouracil/Platinum Chemotherapy in Gastric Cancer.
Keun Wook LEE ; Jee Hyun KIM ; Tak YUN ; Eun Kee SONG ; Im Il NA ; Hyunchoon SHIN ; So Yeon OH ; In Sil CHOI ; Do Youn OH ; Dong Wan KIM ; Seock Ah IM ; Tae You KIM ; Jong Seok LEE ; Dae Seog HEO ; Yung Jue BANG ; Noe Kyeong KIM
Journal of Korean Medical Science 2007;22(Suppl):S115-S121
This study was performed to evaluate the efficacy and toxicity of low-dose paclitaxel/cisplatin chemotherapy in patients with metastatic or recurrent gastric cancer that had failed 5-fluorouracil/platinum-based chemotherapy. Thirty-two patients with documented progression on or within 6 months after discontinuing 5-fluorouracil/platinum-based chemotherapy were enrolled. As a second-line treatment, paclitaxel (145 mg/m2) and cisplatin (60 mg/m2) was administered on day 1 every 3 weeks. Among 32 patients enrolled, 8 (25%) responded partially to paclitaxel/cisplatin, 8 (25%) had stable disease, and 14 (44%) had progressive disease. Two patients (6%) were not evaluable. The median time to progression (TTP) and overall survival for all patients were 2.9 months and 9.1 months, respectively. The most common hematologic toxicity was anemia (47%). Grade 3 neutropenia developed in three patients (9%), but no other grade 3/4 hematologic toxicity occurred. The most common non-hematologic toxicities were emesis (31%) and peripheral neuropathy (38%). Three cases (9%) of grade 3/4 emesis and 2 cases (6%) of grade 3 peripheral neuropathy developed. In conclusion, low-dose paclitaxel and cisplatin chemotherapy showed moderate activity with favorable toxicity profiles. However, relatively short TTP of this regimen warrants the development of more effective paclitaxel-based regimens other than combination with cisplatin in these patients as second-line therapies.
Adenocarcinoma/*drug therapy
;
Adult
;
Aged
;
Antineoplastic Combined Chemotherapy Protocols/*administration & dosage/adverse
;
Cisplatin/administration & dosage/adverse effects
;
Female
;
Fluorouracil/administration & dosage/adverse effects
;
Humans
;
Leucovorin/administration & dosage/adverse effects
;
Male
;
Middle Aged
;
Organoplatinum Compounds/administration & dosage/adverse effects
;
Paclitaxel/administration & dosage/adverse effects
;
Stomach Neoplasms/*drug therapy/mortality
;
Survival Rate
;
Treatment Failure
5.Long-term outcome of kidney transplantation in adult recipients with focal segmental glomerulosclerosis.
Kyu Hun CHOI ; Soon Il KIM ; Soo Young YOON ; Jae Hun KIM ; Shin Wook KANG ; Sung Kyu HA ; Ho Yung LEE ; Dae Suk HAN ; Yu Seun KIM ; Kiil PARK ; Hyeon Joo JEONG ; Dong Kee KIM
Yonsei Medical Journal 2001;42(2):209-214
Focal segmental glomerulosclerosis (FSGS) is an important cause of nephrotic syndrome and end-stage renal disease. FSGS recurrence after renal transplantation has a potentially detrimental course leading to the loss of renal function. In order to establish FSGS recurrence rates and evaluate the course of the disease on living-related-donor renal transplantation in ethnic Korean adults (> or = 18 years), we reviewed our experiences of 27 kidney transplantations with FSGS over the last 15 years. Of the 27 renal allografts, 13 were found to have recurrent FSGS by graft biopsy. In comparison with background data upon patients with and without recurrence of FSGS, the donor age of patients with recurrent FSGS was significantly higher than that of those without recurrence (median, 39 years vs 26, p < 0.05). In terms of, age at transplantation, length of dialysis period, and mode of dialysis no differences were found between recurrent and nonrecurrent cases. The graft survival rate of recipients from a kidney donor of age less than 40 years was significantly higher than that of recipients from a kidney donor of age more than 40 years, at 5 and 10 years, respectively (87% vs 33%, 41% vs 0%, p < 0.05). The association between clinical variables and recurrence was assessed by multiple logistic regression analysis, and donor age was found to be a risk factor of FSGS recurrence (p <0.05). Variables such as HLA-mismatch numbers and immunosuppression were not found to be associated. In conclusion, the recurrence rate of FSGS in adult recipients with FSGS was 48% and patients that received kidney from an older donor appear to be at higher risk of developing recurrence. The use of a renal graft from a younger donor is considered advisable for adult recipients with FSGS.
Adult
;
Female
;
Follow-Up Studies
;
Glomerulosclerosis, Focal/surgery*
;
Human
;
Kidney Transplantation*
;
Male
;
Middle Age
;
Prognosis
;
Recurrence
;
Treatment Outcome
6.Adult-to-Adult Living Donor Liver Transplantation.
Sung Gyu LEE ; Young Joo LEE ; Kwang Min PARK ; Hoon Bae JEON ; Shin HWANG ; Kang Hong LEE ; Rang Kee LEE ; Jung Joon LEE ; Jae Han JUNG ; Won Yong CHOI ; Jin Wook CHOI ; Chul Soo AHN ; Tae Yong HA ; Hoe Jung JUNG ; Byung Chan LEE ; Kyung Suck KOH ; Sang Hoon PARK ; Kyu Taek CHOI ; Yung Sang LEE ; Young Hwa CHUNG ; Dong Jin SUH ; Myung Hwan KIM ; Moon Gyu LEE ; Kyu Bo SUNG ; Mi Kyong KIM ; Hea Seon HA ; Pyung Chul MIN
Journal of the Korean Surgical Society 1998;55(5):719-725
BACKGROUNDS: Living-donor liver transplantation (LDLT) has been established as an efficacious option to resolve the shortage of cadaveric donor organs for pediatric recipients. This surgical innovation has significantly reduced the pretransplantation mortality for children, but the crisis of increasing scarcity of donor organs in our hospital has led us to extend LDLT to adult recipients. However, the extension of LDLT from pediatric recipients to adult recipients has been made only with limited success largely because of the inability of a relatively small-size left-lobe graft to meet the metabolic demands of an adult recipient. It has been postulated that a left-lobe graft smaller than 40% of the recipient's standard liver volume will not result in a successful adult-to-adult LDLT in chronic parenchymal liver disease. METHODS: From February 1997 to October 1997, 10 LDLTs, using 9 extended left-lobe grafts and 1 right-lobe graft, were performed on patients with end-stage parenchymal liver diseases (9 cases of B-hepatitis-induced cirrhosis with or without an associated hepatocellular carcinoma and 1 case of alcoholic cirrhosis) at the Department of Surgery, Asan Medical Center. The ratios of the graft to the standard liver volume of the recipients were in the range of 30% to 55%. RESULTS: All grafts showed immediate function, but delayed normalization of the serum total bilirubin was demonstrated in all recipients receiving left-lobe grafts. There were no mortalities and serious complications in donors. Two recipients died of sepsis 21 days and 40 days after transplantation, and 8 recipients (80%) are alive with good liver function at a median follow-up of 5.1 months (range 2~10 months). CONCLUSIONS: The aim of this article is to report our experience with adult-to-adult LDLT shows that a graft size greater than 30% of the recipient's standard liver volume is able to meet the metabolic demands of adult recipients with chronic parenchymal liver disease and that LDLT might open a new donor pool for adult recipients when the supply of cadaveric organs is severely restricted.
Adult
;
Alcoholics
;
Bilirubin
;
Cadaver
;
Carcinoma, Hepatocellular
;
Child
;
Chungcheongnam-do
;
Fibrosis
;
Follow-Up Studies
;
Humans
;
Liver Diseases
;
Liver Transplantation*
;
Liver*
;
Living Donors*
;
Mortality
;
Sepsis
;
Tissue Donors
;
Transplants
7.Change of Lymphocyte Subsets of HIV-Infected Asymptomatic Persons Administrated with Korean Red Ginseng.
Byeong Sun CHOI ; Yong Keun PARK ; Mee Kyung KEE ; Ok Hyun CHO ; Yong Woo LEE ; Yung Oh SHIN
Journal of the Korean Society of Virology 1997;27(1):97-104
For 16 years after the finding of HIV as an agent of AIDS in 1981, HIV therapeutic drugs of reverse transcriptase inhibitors (AZT, ddI, ddC, d4T) and protease inhibitors have been developed. Recent studies also were focused on a combination therapy by using HIV therapeutic drugs or natural compounds. Korean red ginseng (KRG) of natural compounds has been well known as a good reinforcement agent in Asia. The percentage of CD3+CD4+ T cell in nine HIV-infected patients without KRG treatment averaged 17.8% on baseline and decreased 15.8% after 6 months, whereas the percentage of the cell in fifteen HIV-infected patients with KRG treatment averaged 15.3% on baseline and increased up to 18.9% after the same period. The average percentage of CD3+CD8+ T cell of KRG-nontreated and KRG-treated HIV patients increased after 6 months 47.8% to 50.7% and 44.7% to 51.4%, respectively; and the average percentage of B and NK cell in the KRG-nontreated and KRG-treated HIV patients decreased 9.4% to 7.9% and 13.0% to 9.7%, 8.9% to 8.5% and 16.2% to 11.6%, respectively, KRG, therefore, didn't have any effects on the CD3+CD8+ T cell, B cell, and NK cell. However, it seems that KRG has a potential activity for stimulating the
Asia
;
HIV
;
Humans
;
Killer Cells, Natural
;
Lymphocyte Subsets*
;
Lymphocytes*
;
Panax*
;
Protease Inhibitors
;
Reverse Transcriptase Inhibitors
8.HIV-1 p24 Antigen Detection by Immune Complex Dissociation and Neutralization in HIV-1 Infected Persons in Korea.
Chun KANG ; Sung Soon KIM ; Mee Kyung KEE ; Jeong Gu NAM ; Byung Sun CHOI ; Joo Shil LEE ; Yung Nok LEE ; Jae Chun RYU ; Yung Oh SHIN
Korean Journal of Infectious Diseases 1997;29(5):397-406
BACKGROUND: HIV-1 p24 antigen assay is useful for the detection of circulating viruses, and infection prior to seroconversion. However, circulating HIV-1 p24 antigen may be complexed with HIV antibody and prevent it from being detected by antigen capture assay. To detect HIV-1 p24 antigen in the specimen, it is necessary to dissociate immune complexes and confirm the presence of HIV-1 p24 antigen after the neutralization with the specific antibody. METHODS: We tested 32 sera from HIV-1 infected persons who were diagnosed from 1987 tO1996 in Korea for HIV-1 p24 antigen by enzyme linked immunosorbent assay (ELISA.) with or without the dissociation of immune complexes. And we confirmed the antigen assay results by the neutralization with HIV-1 specific antibody as a confirmatory test. We also calculated the concentration of HIV-1 p24 antigen in each specimen. RESULTS: Eleven of 32 sera tested were initially positive for HIV-1 p24 antigen. After the dissociation of immune complexes for 29 sera except two of which signal/cutoff ratios were higher than 7.0 and except one which was not enough for the assay,13 were shown to be positive for HIV-1 p24 antigen and their signal/cutoff ratios were increased by 10 times. Five of antigen negative cases were turned to be positive after the immune complex dissociation. After neutralization with HIV-1specific p24 antibody for sera of 13 which were positive for HIV-1 p24 antigen with or without the immune complex dissociation, all were shown to be neutralized. We have observed more than 90% neutralization reduction for 12 sera and more than 50% less than 90% for one. The average concentration of HIV-1 p24 antigen was8.76pg/ml by antigen assay and was increased to 76.81~g/m~ after immune complex dissociation. CONCLUSION: We concluded that the sensitivity and the specificity of HIV-1 p24 antigen assay could be increased by dissociation of the immune complexes and neutralization with the specific antibody.
Antigen-Antibody Complex*
;
Enzyme-Linked Immunosorbent Assay
;
HIV
;
HIV-1*
;
Humans
;
Korea*
;
Sensitivity and Specificity
9.Peritoneal Equilibration Test in Korean Patients Undergoing Continuous Ambulatory Peritoneal Dialysis.
Kyu Hun CHOI ; In Hee LEE ; Sug Kyun SHIN ; Hyun Jin NOH ; Shin Wook KANG ; Dong Kee KIM ; Ho Yung LEE ; Dae Suk HAN
Korean Journal of Nephrology 1997;16(3):537-543
In order to evaluate the peritoneal transport characteristics in Korean non-diabetic and diabetic end- stage renal disease patients, peritoneal equilibration test(PET) proposed by Twardowski et al. were performed on patients who had been on continuous ambulatory peritoneal dialysis(CAPD) for 2 to 6 months. The results were as follows : 1) Fifty four patients(including 24 diabetics) on CAPD were studied with a mean age of 48.7 years. And male/female ratio was 1 : 1.08. 2) In non-diabetics, the dialysate to dialysate prior to infusion ratio for glucose(D/D0 glu) at 2-, and 4-hour dwell times were 0.61+/-0.09, and 0.39+/-0.10, and the dialysate-to-plasma ratio for creatinine (D/P cr) at 2-, and 4-hour dwell times were 0.40+/-0.11, 0.63+/-0.12, respectively. 3) In diabetic patients, D/D0 glu at 2-, and 4- hour dwell times were 0.60+/-0.09, 0.39+/-0.08, respectively, and D/P cr at same dwell times were 0.50+/-0.08, and 0.71+/-0.08, which were significantly higher than in non-diabetics(p<0.05). 4) According to the two-hour plasma glucose concentration, diabetic patients were subdivided into hyperglycemic(>or=150mg/dL) and normoglycemic(<150mg/ dL) patients. The values of D/Pcr at 2-, and 4-hour dwell times in hyper-glycemic patients were signficantly higher than in non-diabetic patients (D2/P2 cr : 0.50+/-0.09 vs. 0.40+/-0.11, D4/P4 cr : 0.72+/-0.07 vs 0.63+/-0.12, respectively, p<0.05). 5) Net ultrafiltration did not differ between any of subgroups. 6) In non-diabetic patients, the ranges of D4/P4 cr and D4/D0 glu for high, high average, low average, and low transporters were defined as D4/P4 cr : 0.87-0.75, 0.75-0.63, 0.63-0.51, 0.51-0.39, D4/D0 glu : 0.19-0.29 0.29-0.39, 0.39-0.49, 0.49-0.59, respectively, which were remarkably simliar as suggested by Twardowski et al. In conclusion, the creatinine and glucose transfers assessed by dialysate-plasma ratio of creatinine and glucose are remarkably similar between Korean and North American patients. And the creatinine transport rate in Korean diabetic patient is higher than non-diabetic patient while ultrafiltration is achievable in non-diabetic patient.
Blood Glucose
;
Creatinine
;
Glucose
;
Humans
;
Peritoneal Dialysis, Continuous Ambulatory*
;
Ultrafiltration
10.A Study on Nutritional Status of Iron and Lipids in Infants.
Kwang Hea CHOI ; Son Moon SHIN ; Kee Hwa OH ; Jung Sook SEO ; Kwang Soo KIM ; Yung Sun CHOI
Journal of the Korean Pediatric Society 1995;38(3):297-305
PURPOSE: This study was conducted to get baseline data to establish a guideline for the infant nutrition by observing the feeding practice and nutritional intake during infancy and evaluationg the nutritional status of iron and lipids at 12-month-old infants. METHODS: This survery was cnducted from July to November, 1992. Subjects were healthy infants who were brought to Yeungnam University Hospital for vaccination. We followed up feeding methods for 6 months in 120 infants, and laboratory tests which include hemoglobin, fematocrit, MCHC, ferritin, total cholesterol, HDL-cholesterol, triglyceride and urea nitrogen/creatinine ratio were done in 36 infants at 12 months of age. RESULTS: Male to female sex ratio was 1.6:1 in total 120 study infants. Among 36 infants who took laboratory tests, five infants were breast-fed, 25 were formula-fed, and 6 were mexed-fed. Percentage of the formula-fed infants increased as their monthly age increases. Although 54.2% of the studied infants were started weaning diet at four months of age, 10.8% of infants were not given any weaning diet until 6 month of age. Breastfed infnats had lower hemoglobin(10.6+/-1.8g/dl), hematocrit(32.6+/-3.6%), serum ferritin(13.6+/-13.1ng/ml)(p<0.05), and 15.6% of them had anemia and 16.7% of them had iron deficiency. Serum lipids levels except total cholesterol in breaset-fed female infants were comparable between groups. CONCLUSIONS: We confirm that the incidence of iron deficiency anemia was increased in breast fed infants and there was no difference in lipids levels according to different feeding methods. Adequate iron supplementation through weaning diets is one of the most important problems in breast milk feeding
Anemia
;
Anemia, Iron-Deficiency
;
Breast
;
Cholesterol
;
Diet
;
Feeding Methods
;
Female
;
Ferritins
;
Humans
;
Incidence
;
Infant*
;
Iron*
;
Male
;
Milk, Human
;
Nutritional Status*
;
Sex Ratio
;
Triglycerides
;
Urea
;
Vaccination
;
Weaning

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