1.Effects of General Anesthesia in Patients with Abnormal Liver Function .
Pan Sul LEE ; Ki Nam LEE ; Jun Il MOON ; Chong Hyun LEE
Korean Journal of Anesthesiology 1988;21(4):539-546
Recently, halothane has been commonly used as an inhalation anesthetic agent, but it is generally accepted that it can cause postoperative hepatic dysfunction. Therefore, other anesthetic agents which have relatively less hepatotoxic effects have been recommended. This study was undertaken to evaluate the postoperative hepatic changes in patients with abnormal liver function or hepatobiliary diseases. Patients were divided into three subgroups hepatobiliary, other hepatobiliary and jaundice, or HBsAG(+) for the two anesthetic agents, enflurane and Thalamonal. Liver function tests were performed before surgery, and on the 3rd, 5th and 9th postoperative days. The results were as follows: 1) SGOT and SGPT showed a more statistically significant decrease in Thalamonal anesthesia than in enflurane anesthesia in hepatobiliary and jaundice or HBsAg(+) groups. However, in the other hepatobiliary groups, there were no significant differences between the anesthetics. 2) Total protein, albumin, total bilirubin, direct bilirubin and alkaline phosphatase levels were not shown to be significantly different between the use of the two anesthetics in all groups. It is suggested that postoperative hepatic changes may have improved more significantly in Thalamonal anesthesia than in enflurane anesthesia in hepatobiliary patients with abnormal liver function and jaundice or HBsAg(+) patients.
Alanine Transaminase
;
Alkaline Phosphatase
;
Anesthesia
;
Anesthesia, General*
;
Anesthetics
;
Aspartate Aminotransferases
;
Bilirubin
;
Enflurane
;
Halothane
;
Humans
;
Inhalation
;
Jaundice
;
Liver Function Tests
;
Liver*
2.Clinical Study on Tuberculous Meningitis in Infancy and Childhood.
Jun Hee SUL ; Kee Choon KIM ; Ki Young LEE ; Duk Jin YUN
Journal of the Korean Pediatric Society 1978;21(11):753-761
A clinical study was carried out on 575 cases with tuberculous meningitis who were admitted to the department of pediatrics, Yonsei University College of Medicine during the 18 years from January 1959 to December 1976. The following results were obtained. 1.The age incidence was highest in the age of 2 to 5 and 89.1% were under the age of 8 years. Male to female ratio was 1.5:1 2.The seasonal incidence in order of frequency were spring (30.9%), summer (25.9%), autumn(20.8%) and winter (22.4%). 3. 25% out of the 575 cases had the source of infection infamily members. 4. The tuberculous skin test showed positive reaction in 53.5% 5. The common chief complaints in order of frequency were fever, vomiting, convulsion, unconsciousness and headache. 6. At the time of admission, 80% of 575 cases were diagnosed as meningitis. 7. The major neurologic findings were unconsciousness (34.7%) neck stiffness (86.2%) and positive Kernings sign(62.7%) 8. Chest X-Ray showed normal in 11.6% an miliary tuberculous in 13.7% 9. According to the findings of C.S.F., increased pressure, high protein and low sugar level were associated with poor prognosis. But there were no significant differences on mortality in relation with cell count and chloride level. 10.Mortality rate was 17.5%. Highest mortality was noted in young infants.
Cell Count
;
Female
;
Fever
;
Headache
;
Humans
;
Incidence
;
Infant
;
Male
;
Meningitis
;
Mortality
;
Neck
;
Neurologic Manifestations
;
Pediatrics
;
Prognosis
;
Seasons
;
Seizures
;
Skin Tests
;
Thorax
;
Tuberculosis, Meningeal*
;
Unconsciousness
;
Vomiting
3.Association of Arterial Stiffness and Osteoporosis in Healthy Men Undergoing Screening Medical Examination.
Nam Lee KIM ; Ha Min JANG ; Sul Ki KIM ; Ki Dong KO ; In Cheol HWANG ; Heuy Sun SUH
Journal of Bone Metabolism 2014;21(2):133-141
BACKGROUND: Association of arterial stiffness and osteoporosis has been previously reported in women. However, this association is still controversial for men. Therefore, we investigated correlation of arterial stiffness and osteoporosis by measuring brachial-ankle (ba) pulse wave velocity (PWV) and bone mineral density (BMD). METHODS: We reviewed medical charts of 239 people (women: 128, men: 111) who visited the Health Promotion Center, retrospectively. ba-PWV was measured by automatic wave analyzer. Lumbar spine (L1-L4) BMD and femur BMD were measured by dual energy X-ray absorptiometry. Metabolic syndrome was based on the National Cholesterol Education Program (NCEP)-Adult Treatment Panel (ATPIII) definition. Body mass index (BMI)>25 kg/m2 was used instead of waist circumference. RESULTS: In Pearson's correlation analysis, PWV and femur BMD (Neck, total) had a significant inverse relationship in men (r=-0.254, P=0.007; r=-0.202, P=0.034). In women, PWV and the L-spine, femur (Neck, total) had a significant inverse relationship. (r=-0.321, P<0.001; r=-0.189, P=0.032; r=-0.177, P=0.046) Age and PWV showed the greatest association in both men and women (r=0.46 P<0.001; r=0.525, P<0.001) In multiple regression analysis, the L-spine BMD and PWV had an independent relationship in women after adjusting for age, metabolic syndrome, BMI, smoking, drinking and exercise. (r=-0.229, P=0.015). No independent association was found between PWV and BMD in men. CONCLUSIONS: The association between arterial stiffness and BMD was confirmed in women. However, this association was not statistically significant for men.
Absorptiometry, Photon
;
Body Mass Index
;
Bone Density
;
Cholesterol
;
Drinking
;
Education
;
Female
;
Femur
;
Health Promotion
;
Humans
;
Male
;
Mass Screening*
;
Osteoporosis*
;
Pulse Wave Analysis
;
Retrospective Studies
;
Smoke
;
Smoking
;
Spine
;
Vascular Stiffness*
;
Waist Circumference
4.A Case of Uhls Anomaly.
Jun Hee SUL ; Ki Chun KIM ; Ki Sub CHUNG ; Sung Kyu LEE ; Chang Jin KIM ; Jae Yun RHO
Journal of the Korean Pediatric Society 1979;22(6):476-480
Congenital hypoplasia of the right ventricular myocardium, also known as parchment heart or Uhl's anomaly, is a rare congenital heart defect. It was first described in Oslers principles and Practice of Medicine in 1905 and reviewed by Segall We found 29 reported cases, but there was no reported case in Korea. Recently, we experienced a case of Uhls anomaly associated with patent ductus arteriosus, atrial septal defect, pulmonary atresia and tricuspid abnormality in a 3 month-old infant, which was confirmed by autopsy. We present a case with a brief review of litteratures.
Autopsy
;
Ductus Arteriosus, Patent
;
Heart
;
Heart Defects, Congenital
;
Heart Septal Defects, Atrial
;
Humans
;
Infant
;
Korea
;
Myocardium
;
Pulmonary Atresia
5.A Measurement of Rubella Antibodies among Korean Children by Enzyme-linked Immunosorbent Assay.
Ki Young LEE ; Jun Hee SUL ; Young Nam LEE ; Chang Hee KIM ; Joo Deuk KIM
Yonsei Medical Journal 1981;22(1):41-48
We measured the degree of immunity of 326 Korean children to rubella virus by enzyme-linked immunosorbent assy (ELISA). They were admitted to Pediatrics Unit of Yonsei Medical Center between April and July, 1980 with various illnesses excluding rubella disease. Among the 326 tested, 172 cases gave a positive titer of antibodies (mainly, IgG and IgM antibodies) and 127 had IgG antibody against rubella virus antigen. These represented 52.8% and 39.0%, respectively, of the total number of children tested. There was no significant difference in the rate of positivity between sex, but the positive rate increased as the age increased. The antobody titers of positive individuals to rubella virus were higher among the older children. Results and a brief outline of the ELISA method for serodiagnosis of rubella in clinical use will be discussed.
Adolescent
;
Age Factors
;
Antibodies, Viral/analysis*
;
Child
;
Child, Preschool
;
Enzyme-Linked Immunosorbent Assay*
;
Female
;
Human
;
Immunoenzyme Techniques*
;
Infant
;
Infant, Newborn
;
Korea
;
Male
;
Rubella/immunology
;
Rubella virus/immunology*
6.A New Direction for Teaching Medical Ethics .
Eun Sul LEE ; Mi Sook SONG ; Ki Young LIM ; Ho Young LEE
Korean Journal of Medical Education 1995;7(1):59-65
Drawing on our observation that many medical professionals have considerable difficulty in using what they know about ethics, we have developed a course for teaching the fifth year medical students a systematic approach to ethical reasoning and problem-solving, rather than teaching bioethical theories or prominent current ethical issues in developed countries. This course consisted of a series of guided group discussions and debates in classroom using over 50 cases classified under seven major headings. Responses and reactions from students and participating clinicians are encouraging. Several ideas for improving medical ethics curricula are discussed, including emphases on the thorough understanding of various aspects of human relations in medical practice, enhancing the ability of articulate the students own values, provoking the student to get involved in the ethical situation when studying the cases, and the need to introduce social science concepts in analyzing the ethical issues in the health care system.
Curriculum
;
Delivery of Health Care
;
Developed Countries
;
Ethics
;
Ethics, Medical*
;
Head
;
Humans
;
Social Sciences
;
Students, Medical
7.Improvement of Frontal Lobe Dysfunctions in Neuromyelitis Optica after Treatment: A Case Report.
Jaejeong JOO ; Sul Ki LEE ; In Ha HWANG ; Kyum Il KWON ; Byoung June AHN ; Youngsoon YANG
Dementia and Neurocognitive Disorders 2016;15(1):20-23
BACKGROUND: Neuromyelitis optica (NMO) is characterized by optic neuritis and longitudinally extensive transverse myelitis. Generally, the brain had been considered healthy in NMO patients, though recent studies have demonstrated that T2-weighted abnormalities may be observed in various brain regions. Logically, NMO brain lesions are localized at sites of high aquaporin-4 expression. CASE REPORT: A 68-year-old right-handed man with dysuria, weakness in the bilateral upper and lower limbs, and decreased sensation of the lower extremities, was diagnosed with neuromyelitis optica. The patient was gradually speaking less, was showing reduced interest in hobbies, and had undergone changes in character and behavior. An examination was performed using the Seoul Neuropsychological Screening Battery (SNSB), which revealed that the profile of frontal lobe dysfunctions was prominent as compared with other cognitive domains. The patient was treated with prednisolone and azathioprine for about 1 year without recurrence, and showed prognostic improvement according to further SNSB testing. CONCLUSIONS: Further studies are considered necessary in order to find the most effective medication regimen for improving cognitive functions in those accurately diagnosed with NMO, and to develop systematic treatment using even more diversified immune-related agents.
Aged
;
Azathioprine
;
Brain
;
Dysuria
;
Frontal Lobe*
;
Hobbies
;
Humans
;
Logic
;
Lower Extremity
;
Mass Screening
;
Myelitis, Transverse
;
Neuromyelitis Optica*
;
Optic Neuritis
;
Prednisolone
;
Recurrence
;
Sensation
;
Seoul
8.A case of Scurvy.
Jun Hee SUL ; Chul LEE ; Duk Hee KIM ; Pyung Kil KIM ; Duk Jin YUN ; Ki Keun OH
Journal of the Korean Pediatric Society 1980;23(9):730-736
Scurvy is a manifestation of deficiency of vitamin C, which was characterized by follicular hyperkeratosis, hemorrhagic manifestation, fatigue, muscular ache and pains, swollen jonts, swollen bleeding gums, and peripheral edema. Rescently we experienced a cases of scurvy in 13 month old boy who had been nourished by artificial feedings with ricegruel without additional vitamin C. Rentgenographic findings of bone revealed rosaries in all costochondral junctions and typical scorvutic changes in both femur. Scury is very rare disease in korea now. A brief review of literature was done.
Ascorbic Acid
;
Edema
;
Femur
;
Gingiva
;
Hemorrhage
;
Humans
;
Infant
;
Korea
;
Male
;
Muscle Fatigue
;
Rare Diseases
;
Scurvy*
9.Posterior Cortical Atrophy with Acute Onset and Rapid Progressive Visual Symptoms: A Case Report.
Jaejeong JOO ; Sul Ki LEE ; In Ha HWANG ; Kyum Il KWON ; Byoung June AHN ; Youngsoon YANG
Dementia and Neurocognitive Disorders 2015;14(2):83-86
BACKGROUND: Posterior cortical atrophy (PCA) is characterized by slowly progressive early onset dementia with cortical visual dysfunction and disproportionate atrophy of the posterior cortex. CASE REPORT: A 55-year-old right-handed woman developed visuo-spatial impairments that progressed rapidly into cortical blindness over the following 3 months. Neuro-psychological evaluation revealed Gerstmann syndrome and severe constructional impairments with all components of Balint syndrome. However, her memory, insight, and judgment were preserved. Her brain MRI was normal. However, 18F fluorodeoxyglucose positron emission tomography revealed a marked hypometabolism in the bilateral parieto-occipital region. CONCLUSIONS: Although rapid progression of visuo-spatial dysfunction without memory impairment occurred, we considered PCA as well.
Atrophy*
;
Blindness, Cortical
;
Brain
;
Dementia
;
Female
;
Fluorodeoxyglucose F18
;
Gerstmann Syndrome
;
Humans
;
Judgment
;
Magnetic Resonance Imaging
;
Memory
;
Middle Aged
;
Passive Cutaneous Anaphylaxis
;
Positron-Emission Tomography
10.A clinical study on 24 cases of renal transplantation.
Seung Hun SHIN ; Min Soo JEONG ; Sunn Kgoo RHEE ; Jeong Ho LEE ; Gang Wook YI ; Young Tai SHIN ; Ki Sub SON ; Wan Hee YOON ; Chong Koo SUL
Korean Journal of Nephrology 1991;10(3):401-411
No abstract available.
Kidney Transplantation*