2.The Future of Research on Extracorporeal Membrane Oxygenation (ECMO).
Korean Journal of Critical Care Medicine 2016;31(2):73-75
No abstract available.
Extracorporeal Membrane Oxygenation*
3.Toward Unity of the Mind and Body.
Journal of Korean Neuropsychiatric Association 2010;49(3):287-290
No abstract available.
4.Somatiaztion disorder.
Journal of the Korean Academy of Family Medicine 2001;22(8):1153-1162
No abstract available.
5.Psychiatric Disorders in Primary Care Setting.
Journal of the Korean Medical Association 1997;40(12):1663-1671
No abstract available.
Primary Health Care*
6.Effects of Alcohol-Related Factors on Drinking Behaviors and Problematic Sexual Behaviors in College Students.
Korean Journal of Health Promotion 2011;11(2):91-99
BACKGROUND: The purpose of this study was to explore the relationships between psychosocial stress, alcohol expectancy, drinking refusal self-efficacy, and drinking behaviors with problematic sexual behaviors in college students. METHODS: Participants were college students (129 males, 67 females) with a mean age of 22.6 years old. Data analysis was done with SPSS 13.0 for descriptive statistics and LISREL 8.53 program for path analysis. RESULTS: The path model showed a good fit to the empirical data (chi2=10.14, P=0.71, GFI=0.98, AGFI=0.94, CFI=0.96, RMSEA=0.07). Our analysis showed that psychosocial stress, drinking refusal self-efficacy, and alcohol expectancy had a significant direct effect on drinking behaviors and that drinking behaviors had a significant direct effect on problematic sexual behaviors. CONCLUSIONS: These findings suggest that alcohol prevention or education programs should emphasize stress management and refusal skills training to prevent college students from drinking behaviors and problematic sexual behaviors at the highest risk for various stressors and heavy drinking.
Alcohols
;
Disulfiram
;
Drinking
;
Drinking Behavior
;
Humans
;
Male
;
Sexual Behavior
;
Statistics as Topic
7.Prurigo Pigmentosa after Injection Lypolysis with Phosphatidylcholine and Deoxycholate.
Korean Journal of Dermatology 2016;54(8):673-674
No abstract available.
Deoxycholic Acid*
;
Phosphatidylcholines*
;
Prurigo*
8.Alfa - difluoromethylornithine Reduced Protein Phosphorylation in MCF-7 Human Breast Cancer Cells.
Journal of the Korean Cancer Association 1999;31(5):1044-1053
No abstract available.
Breast Neoplasms*
;
Breast*
;
Eflornithine*
;
Estrogens
;
Humans*
;
MCF-7 Cells
;
Phosphorylation*
;
Polyamines
9.In Vitro Perfusion Studies on Coronary Function of Cardiac Ischemia-Reperfusion in Spontaneously Hypertensive Rat Heart.
Korean Circulation Journal 1995;25(1):59-67
BACKGROUND: Myocardial ischemia in human hypertension and in various animal models of hypertension may be due to abnormal maximal coronary vasodilator reserve and disturbaces of coronary vasomotion. The vascular reactivity defects in hypertension have been associated with the defective endothelium and sympathetic neural activation. However, such abnormalities in hypertension need to be elucidated. In the present study the effectsof cardiac ischemia reperfusion on coronary circulation, intramyocytic adenylates and purine nucleosides were examined in Langendorff-perfused Sprague Dawley rat (SD) and spontaneously hypertensive rat (SHR) hearts. Coronary venous and cardiac lactate and cardiac pyruvate were also measured. It should be noted that in the regulation of coronary flow the intrinsic flow autoregulation is highly variable due to coexisting metabolic flow control, and that natural coronary flow and cardiomyocytic energy state are normally reciprocally related in perfused heart. METHODS: For the Langendorff heart perfusion, bicarbonate perfusion buffer (pH 7.40+/-0.02,37degrees C) was equilibrated with 95% O2 : 5% CO2 and contained 5mM glucose (+5U/1 insulin) and 2mM pyruvate as energy-yielding substrates. Global hypoperfusion ischemia was induced by lowering coronary perfusion pressure of 100 to 40 cmH2O, followed by 20 min reperfusion. RESULTS: During the ischemia and reperfusion, metabolic acidosis and enhanced venous lactate output in SHR were observed with increases in coronary vascular resistance and myocardial oxygen consumption.In addition, coronary reactive hyperemia during reperfusion was depressed. Although ischemia-induced increase in combined adenosine plus inosine were abolished during prolonged reperfusion, SD still exhibited coronary vasodilation. The depressed reactive hyperemia in SHR was associated with decreases in cardiac adenosine triphosphate (ATP) pool and creatine phosphate/inorganic phosphate (CrP/Pi) ratio and an increase in cardiac lactate/pyruvate ratio. CONCLUSION: This abnormal vascular reactivity during ischemia and reperfusion in SHR may be in part due to an alteration in the cardiac energy state and hence to a mismatch between myocardial metabolic demand and supply.
Acidosis
;
Adenosine
;
Adenosine Triphosphate
;
Animals
;
Coronary Circulation
;
Creatine
;
Endothelium
;
Glucose
;
Heart*
;
Homeostasis
;
Humans
;
Hyperemia
;
Hypertension
;
Inosine
;
Ischemia
;
Lactic Acid
;
Models, Animal
;
Myocardial Ischemia
;
Oxygen
;
Perfusion*
;
Purine Nucleosides
;
Pyruvic Acid
;
Rats
;
Rats, Inbred SHR*
;
Reperfusion
;
Vascular Resistance
;
Vasodilation
10.Predisposing Hemodynamic Factors Associated with a Failed Apnea Test during Brain Death Determination.
Korean Journal of Critical Care Medicine 2016;31(3):236-242
BACKGROUND: The apnea test is an essential component in the clinical determination of brain death, however it may incur a significant risk of complications such as hypotension, hypoxia and even cardiac arrest. We analyzed the risk factors associated with a failed apnea test during brain death assessment in order to predict and avoid these adverse events. METHODS: Medical records on apnea tests performed for brain-dead donors at our institution between January 2009 and January 2016 were retrospectively reviewed. Age, gender, etiology of brain death, use of catecholamines and results of arterial blood gas analysis (ABGA), systolic/diastolic blood pressure (SBP/DBP), mean arterial pressure and central venous pressure prior to apnea test initiation were collected as variables. A-a gradient and P(aO2)/F(iO2) were calculated for more precise assessment of the respiratory system. In total, 267 cases were divided into two groups based on those who completed the apnea test and those who failed the test. RESULTS: 13 cases failed the apnea test. Among them, seven cases failed due to severe hypotension (SBP < 60 mmHg) and the others failed due to refractory hypoxia. In terms of hemodynamic state, SBP was significantly higher in the completed test group than the failed group (126.5 ± 23.9 vs. 103 ± 15.2, respectively; p = 0.001). In ABGA, the completed test group showed significantly higher P(aO2)/F(iO2) (313.6 ± 229.8 vs. 141.5 ± 131.0, respectively; p = 0.008) and a lower A-a gradient (278.2 ± 209.5 vs. 506.2 ± 173.1, respectively; p = 0.000). In multivariable analysis, low SBP (p = 0.003) and high A-a gradient (p = 0.044) were independent risk factors associated with a failed apnea test. CONCLUSIONS: Although the unexpected adverse events during the apnea test for brain death determination do not occur frequently, they can be fatal. If a brain-dead patient has low SBP and a high A-a gradient, clinicians should pay more attention and prepare for potential complications prior to the apnea test.
Anoxia
;
Apnea*
;
Arterial Pressure
;
Blood Gas Analysis
;
Blood Pressure
;
Brain Death*
;
Brain*
;
Catecholamines
;
Causality
;
Central Venous Pressure
;
Heart Arrest
;
Hemodynamics*
;
Humans
;
Hypotension
;
Medical Records
;
Respiratory System
;
Retrospective Studies
;
Risk Factors
;
Tissue Donors