1.Impact of Anticoagulation Intensity in Korean Patients with Atrial Fibrillation: Is It Different from Western Population?
Ki Hong LEE ; Jeong Gwan CHO ; Nuri LEE ; Kyung Hoon CHO ; Hyung Ki JEONG ; Hyukjin PARK ; Yongcheol KIM ; Jae Yeong CHO ; Min Chul KIM ; Doo Sun SIM ; Hyun Ju YOON ; Namsik YOON ; Kye Hun KIM ; Young Joon HONG ; Hyung Wook PARK ; Youngkeun AHN ; Myung Ho JEONG ; Jong Chun PARK
Korean Circulation Journal 2020;50(2):163-175
BACKGROUND AND OBJECTIVES: Although anticoagulation with warfarin is recommended as an international normalized ratio (INR) of prothrombin time between 2.0 and 3.0 and mean time in the therapeutic range (TTR) ≥70%, little has been proven that universal criteria might be suitable in Korean atrial fibrillation (AF) patients.METHODS: We analyzed 710 patients with non-valvular AF who took warfarin. INR value and clinical outcomes were assessed during 2-year follow-up. Intensity of anticoagulation was assessed as mean INR value and TTR according to target INR range. Primary net-clinical outcome was defined as the composite of new-onset stroke and major bleeding. Secondary net-clinical outcome was defined as the composite of new-onset stroke, major bleeding and death.RESULTS: Thromboembolism was significantly decreased when mean INR was over 1.6. Major bleeding was significantly decreased when TTR was over 70% and mean INR was less than 2.6. Mean INR 1.6–2.6 significantly reduced thromboembolism (adjusted hazard ratio [HR], 0.40; 95% confidence interval [CI], 0.19–0.85), major bleeding (HR, 0.43; 95% CI, 0.23–0.81), primary (HR, 0.50; 95% CI, 0.29–0.84) and secondary (HR, 0.45; 95% CI, 0.28–0.74) net-clinical outcomes, whereas mean INR 2.0–3.0 did not. Simultaneous satisfaction of mean INR 1.6–2.6 and TTR ≥70% was associated with significant risk reduction of major bleeding, primary and secondary net-clinical outcomes.CONCLUSIONS: Mean INR 1.6–2.6 was better than mean INR 2.0–3.0 for the prevention of thromboembolism and major bleeding. However, INR 1.6–2.6 and TTR ≥70% had similar clinical outcomes to INR 2.0–3.0 and TTR ≥70% in Korean patients with non-valvular AF.
Atrial Fibrillation
;
Follow-Up Studies
;
Hemorrhage
;
Humans
;
International Normalized Ratio
;
Prothrombin Time
;
Risk Reduction Behavior
;
Stroke
;
Thromboembolism
;
Warfarin
2.Benefit of Early Statin Initiation within 48 Hours after Admission in Statin-Naïve Patients with Acute Myocardial Infarction Undergoing Percutaneous Coronary Intervention
Min Chul KIM ; Youngkeun AHN ; Jae Yeong CHO ; Ki Hong LEE ; Doo Sun SIM ; Nam Sik YOON ; Hyun Ju YOON ; Kye Hun KIM ; Young Joon HONG ; Hyung Wook PARK ; Ju Han KIM ; Myung Ho JEONG ; Jeong Gwan CHO ; Jong Chun PARK ; Kiyuk CHANG ; Ki Bae SEUNG
Korean Circulation Journal 2019;49(5):419-433
BACKGROUND AND OBJECTIVES: Although current guidelines recommend early initiation of statin in patients with acute myocardial infarction (AMI), there is no consensus for optimal timing of statin initiation. METHODS: A total of 3,921 statin-naïve patients undergoing percutaneous coronary intervention were analyzed, and divided into 3 groups according to statin initiation time: group 1 (statin initiation <24 hours after admission), group 2 (24–48 hours) and group 3 (≥48 hours). We also made 3 stratified models to reduce bias: model 1 (<24 hours vs. ≥24 hours), model 2 (<48 hours vs. ≥48 hours) and model 3 (<24 hours vs. 24–48 hours). The endpoint was major adverse cardiac events (MACE; composite of cardiac death, myocardial infarction and target-vessel revascularization) during median 3.8 years. RESULTS: During follow-up, incidence of MACE was lower in early statin group in both model 1 (14.3% vs. 18.4%, hazard ratio [HR], 0.77; 95% confidence interval [CI], 0.66–0.91; p=0.002) and model 2 (14.6% vs. 19.7%, HR, 0.81; 95% CI, 0.67–0.97; p=0.022). After propensity-score matching, results remained unaltered. Statin initiation <24 hours reduced MACE compared to statin initiation ≥24 hours in model 1. Statin initiation <48 hours also reduced MACE compared to statin initiation later in model 2. However, there was no difference in incidence of MACE between statin initiation <24 hours and 24–48 hours) in model 3. CONCLUSIONS: Early statin therapy within 48 hours after admission in statin-naïve patients with AMI reduced long-term clinical outcomes compared with statin initiation later. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT02385682
Bias (Epidemiology)
;
Consensus
;
Death
;
Follow-Up Studies
;
Humans
;
Hydroxymethylglutaryl-CoA Reductase Inhibitors
;
Incidence
;
Myocardial Infarction
;
Percutaneous Coronary Intervention
3.Vitamin D Deficiency/Insufficiency among Inpatients with Depressive Symptoms
Young Sup WOO ; Sangha KIM ; Jong Hyun JEONG ; Young Eun JUNG ; Moon Doo KIM ; Won Myong BAHK
Clinical Psychopharmacology and Neuroscience 2019;17(1):121-124
OBJECTIVE: Although the association between low vitamin D levels and depressive symptoms has been widely reported, studies investigating the relationship between hypovitaminosis D and depressive symptomatology are scarce. METHODS: We retrospectively studied the relationship between vitamin D status and depressive symptoms in 196 patients hospitalized for a major depressive episode. RESULTS: The baseline 17-item Hamilton Depression Rating Scale total and depression factor (item 1, 2, 3, 7) scores were significantly higher in the vitamin-D-insufficiency/deficiency group than in the vitamin-D-sufficiency group. CONCLUSION: It is important to consider measuring the vitamin D levels of patients with severe and core depressive symptoms and providing vitamin D supplementation when necessary.
Anhedonia
;
Depression
;
Humans
;
Inpatients
;
Retrospective Studies
;
Vitamin D
;
Vitamins
4.Korean Medication Algorithm for Bipolar Disorder 2018: Comparisons with Other Treatment Guidelines
Jong Hyun JEONG ; Won Myong BAHK ; Young Sup WOO ; Jung Goo LEE ; Moon Doo KIM ; InKi SOHN ; Se Hoon SHIM ; Duk In JON ; Jeong Seok SEO ; Won KIM ; Hoo Rim SONG ; Kyung Joon MIN ; Bo Hyun YOON
Clinical Psychopharmacology and Neuroscience 2019;17(2):155-169
The objective of this study was to compare recommendations of the Korean Medication Algorithm Project for Bipolar Disorder 2018 (KMAP-BP 2018) with other recently published guidelines for treating bipolar disorder. We reviewed a total of five recently published global treatment guidelines and compared treatment recommendation of the KMAP-BP 2018 with those of other guidelines. For initial treatment of mania, there were no significant differences across treatment guidelines. All guidelines recommended mood stabilizer (MS) or atypical antipsychotic (AAP) monotherapy or a combination of an MS with an AAP as a first-line treatment strategy for mania. However, the KMAP-BP 2018 did not prefer monotherapy with MS or AAP for psychotic mania. Quetiapine, olanzapine and aripiprazole were the first-line AAPs for nearly all phases of bipolar disorder across guidelines. Most guidelines advocated newer AAPs as first-line treatment options for all phases while lamotrigine was recommended for depressive and maintenance phases. Lithium and valproic acid were commonly used as MSs in all phases of bipolar disorder. As research evidence accumulated over time, recommendations of newer AAPs (such as asenapine, cariprazine, paliperidone, lurasidine, long-acting injectable risperidone and aripiprazole once monthly) became prominent. KMAP-BP 2018 guidelines were similar to other guidelines, reflecting current changes in prescription patterns for bipolar disorder based on accumulated research data. Strong preference for combination therapy was characteristic of KMAP-BP 2018, predominantly in the treatment of psychotic mania and severe depression. Further studies were needed to address several issues identified in our review.
Aripiprazole
;
Bipolar Disorder
;
Depression
;
Drug Therapy
;
Lithium
;
Paliperidone Palmitate
;
Prescriptions
;
Quetiapine Fumarate
;
Risperidone
;
Valproic Acid
5.Validation of the Korean Version of the Depression in Old Age Scale and Comparison with Other Depression Screening Questionnaires Used in Elderly Patients in Medical Settings
Young Eun JUNG ; Moon Doo KIM ; Won Myong BAHK ; Young Sup WOO ; Beomwoo NAM ; Jeong Seok SEO ; Sae Heon JANG ; Hyung Mo SUNG ; In Hee SHIM ; Bo Hyun YOON ; Ji Sun KIM ; Young Joon KWON
Clinical Psychopharmacology and Neuroscience 2019;17(3):369-376
OBJECTIVE: The Depression in Old Age Scale (DIA-S) is a new screening tool for assessing depression in the elderly. The primary aims of this study were to describe the validation of the Korean version of the DIA-S (K-DIA-S) and to compare its validity with that of other depression screening questionnaires used in elderly outpatients in medical settings. METHODS: A total of 385 elderly outpatients completed the K-DIA-S and underwent the Mini International Neuropsychiatric Interview to diagnose depressive disorders. Other measures included the 15-item short form of the Geriatric Depression Scale (SGDS), the 9-item depression module of the Patient Health Questionnaire (PHQ-9), and the Montgomery–Asberg Depression Rating Scale (MADRS). Reliability and validity tests, an optimal cutoff point estimate, and receiver operating characteristic curve analysis were performed to investigate the diagnostic validity of the K-DIA-S. Areas under the curves (AUCs) for the K-DIA-S, SGDS, and PHQ-9 were compared statistically. RESULTS: The K-DIA-S showed good internal consistency and strong correlations with the SGDS (r = 0.853), PHQ-9 (r = 0.739), and MADRS (r = 0.772). The cut-off point of the K-DIA-S that can be recommended for screening depressive symptoms was a score of 4. For “any depressive disorder”, the AUC (standard error) for the K-DIA-S was 0.896 (0.015), which was significantly larger than that for the PHQ-9 (p = 0.033). CONCLUSION: The present findings suggest that the K-DIA-S has good psychometric properties and is a valid and reliable tool for assessing depressive symptoms in elderly populations and medically ill patients.
Aged
;
Area Under Curve
;
Depression
;
Depressive Disorder
;
Humans
;
Mass Screening
;
Outpatients
;
Psychometrics
;
Reproducibility of Results
;
ROC Curve
6.Efficacy and Safety of Voglibose Plus Metformin in Patients with Type 2 Diabetes Mellitus: A Randomized Controlled Trial
Tae Jung OH ; Jae Myung YU ; Kyung Wan MIN ; Hyun Shik SON ; Moon Kyu LEE ; Kun Ho YOON ; Young Duk SONG ; Joong Yeol PARK ; In Kyung JEONG ; Bong Soo CHA ; Yong Seong KIM ; Sei Hyun BAIK ; In Joo KIM ; Doo Man KIM ; Sung Rae KIM ; Kwan Woo LEE ; Jeong Hyung PARK ; In Kyu LEE ; Tae Sun PARK ; Sung Hee CHOI ; Sung Woo PARK
Diabetes & Metabolism Journal 2019;43(3):276-286
BACKGROUND: Combination of metformin to reduce the fasting plasma glucose level and an α-glucosidase inhibitor to decrease the postprandial glucose level is expected to generate a complementary effect. We compared the efficacy and safety of a fixed-dose combination of voglibose plus metformin (vogmet) with metformin monotherapy in drug-naïve newly-diagnosed type 2 diabetes mellitus. METHODS: A total of 187 eligible patients aged 20 to 70 years, with a glycosylated hemoglobin (HbA1c) level of 7.0% to 11.0%, were randomized into either vogmet or metformin treatments for 24 weeks. A change in the HbA1c level from baseline was measured at week 24. RESULTS: The reduction in the levels of HbA1c was −1.62%±0.07% in the vogmet group and −1.31%±0.07% in the metformin group (P=0.003), and significantly more vogmet-treated patients achieved the target HbA1c levels of <6.5% (P=0.002) or <7% (P=0.039). Glycemic variability was also significantly improved with vogmet treatment, estimated by M-values (P=0.004). Gastrointestinal adverse events and hypoglycemia (%) were numerically lower in the vogmet-treated group. Moreover, a significant weight loss was observed with vogmet treatment compared with metformin (−1.63 kg vs. −0.86 kg, P=0.039). CONCLUSION: Vogmet is a safe antihyperglycemic agent that controls blood glucose level effectively, yields weight loss, and is superior to metformin in terms of various key glycemic parameters without increasing the risk of hypoglycemia.
Blood Glucose
;
Diabetes Mellitus, Type 2
;
Fasting
;
Glucose
;
Hemoglobin A, Glycosylated
;
Humans
;
Hypoglycemia
;
Metformin
;
Weight Loss
7.Cavernous Hemangioma of the Gallbladder: a Case Report
Jae Hwi PARK ; Jeong Sub LEE ; Guk Myung CHOI ; Bong Soo KIM ; Seung Hyoung KIM ; JeongJae KIM ; Doo Ri KIM ; Chang Lim HYUN ; Kyu Hee HER
Investigative Magnetic Resonance Imaging 2019;23(3):264-269
Cavernous hemangioma of the gallbladder is an extremely rare benign tumor. The tumor has only a few cases being reported in literature. However, to the best of our knowledge, no reports focusing on the MRI findings of cavernous hemangioma of the gallbladder have been published. This study reports a case of gallbladder hemangioma with pathologic and radiologic reviews, including MRI findings.
Gallbladder
;
Hemangioma
;
Hemangioma, Cavernous
;
Magnetic Resonance Imaging
8.Influence of Local Myocardial Infarction on Endothelial Function, Neointimal Progression, and Inflammation in Target and Non-Target Vascular Territories in a Porcine Model of Acute Myocardial Infarction
Hyun Kuk KIM ; Han Byul KIM ; Joo Myung LEE ; Sung Soo KIM ; In Ho BAE ; Dae Sung PARK ; Jun Kyu PARK ; Jae Won SHIM ; Joo Young NA ; Min Young LEE ; Joong Sun KIM ; Doo Sun SIM ; Young Joon HONG ; Chang Wook NAM ; Joon Hyung DOH ; Jonghanne PARK ; Bon Kwon KOO ; Sun Uk KIM ; Kyung Seob LIM ; Myung Ho JEONG
Journal of Korean Medical Science 2019;34(19):e145-
BACKGROUND: Patients with acute myocardial infarction (AMI) have worse clinical outcomes than those with stable coronary artery disease despite revascularization. Non-culprit lesions of AMI also involve more adverse cardiovascular events. This study aimed to investigate the influence of AMI on endothelial function, neointimal progression, and inflammation in target and non-target vessels. METHODS: In castrated male pigs, AMI was induced by balloon occlusion and reperfusion into the left anterior descending artery (LAD). Everolimus-eluting stents (EES) were implanted in the LAD and left circumflex (LCX) artery 2 days after AMI induction. In the control group, EES were implanted in the LAD and LCX in a similar fashion without AMI induction. Endothelial function was assessed using acetylcholine infusion before enrollment, after the AMI or sham operation, and at 1 month follow-up. A histological examination was conducted 1 month after stenting. RESULTS: A total of 10 pigs implanted with 20 EES in the LAD and LCX were included. Significant paradoxical vasoconstriction was assessed after acetylcholine challenge in the AMI group compared with the control group. In the histologic analysis, the AMI group showed a larger neointimal area and larger area of stenosis than the control group after EES implantation. Peri-strut inflammation and fibrin formation were significant in the AMI group without differences in injury score. The non-target vessel of the AMI also showed similar findings to the target vessel compared with the control group. CONCLUSION: In the pig model, AMI events induced endothelial dysfunction, inflammation, and neointimal progression in the target and non-target vessels.
Acetylcholine
;
Arteries
;
Balloon Occlusion
;
Constriction, Pathologic
;
Coronary Artery Disease
;
Drug-Eluting Stents
;
Endothelium
;
Fibrin
;
Follow-Up Studies
;
Humans
;
Inflammation
;
Male
;
Myocardial Infarction
;
Reperfusion
;
Stents
;
Swine
;
Vasoconstriction
9.Normal Reference Plots for the Bioelectrical Impedance Vector in Healthy Korean Adults
Jun Hyok OH ; Seunghwan SONG ; Harin RHEE ; Sun Hack LEE ; Doo Youp KIM ; Jeong Cheon CHOE ; Jinhee AHN ; Jin Sup PARK ; Myung Jun SHIN ; Yun Kyung JEON ; Hye Won LEE ; Jung Hyun CHOI ; Han Cheol LEE ; Kwang Soo CHA
Journal of Korean Medical Science 2019;34(30):e198-
BACKGROUND: Accurate volume measurement is important in the management of patients with congestive heart failure or renal insufficiency. A bioimpedance analyser can estimate total body water in litres and has been widely used in clinical practice due to its non-invasiveness and ease of results interpretation. To change impedance data to volumetric data, bioimpedance analysers use equations derived from data from healthy subjects, which may not apply to patients with other conditions. Bioelectrical impedance vector analysis (BIVA) was developed to overcome the dependence on those equations by constructing vector plots using raw impedance data. BIVA requires normal reference plots for the proper interpretation of individual vectors. The aim of this study was to construct normal reference vector plots of bioelectrical impedance for Koreans. METHODS: Bioelectrical impedance measurements were collected from apparently healthy subjects screened according to a comprehensive physical examination and medical history performed by trained physicians. Reference vector contours were plotted on the RXc graph using the probability density function of the bivariate normal distribution. We further compared them with those of other ethnic groups. RESULTS: A total of 242 healthy subjects aged 22 to 83 were recruited (137 men and 105 women) between December 2015 and November 2016. The centers of the tolerance ellipses were 306.3 Ω/m and 34.9 Ω/m for men and 425.6 Ω/m and 39.7 Ω/m for women. The ellipses were wider for women than for men. The confidence ellipses for Koreans were located between those for Americans and Spaniards without overlap for both genders. CONCLUSION: This study presented gender-specific normal reference BIVA plots and corresponding tolerance and confidence ellipses on the RXc graph, which is important for the interpretation of BIA-reported volume status in patients with congestive heart failure or renal insufficiency. There were noticeable differences in reference ellipses with regard to gender and ethnic groups.
Adult
;
Blood Volume
;
Body Fluid Compartments
;
Body Water
;
Electric Impedance
;
Ethnic Groups
;
Female
;
Healthy Volunteers
;
Heart Failure
;
Humans
;
Male
;
Physical Examination
;
Renal Insufficiency
10.Erratum: Correction of Figure in the Article: Normal Reference Plots for the Bioelectrical Impedance Vector in Healthy Korean Adults
Jun Hyok OH ; Seunghwan SONG ; Harin RHEE ; Sun Hack LEE ; Doo Youp KIM ; Jeong Cheon CHOE ; Jinhee AHN ; Jin Sup PARK ; Myung Jun SHIN ; Yun Kyung JEON ; Hye Won LEE ; Jung Hyun CHOI ; Han Cheol LEE ; Kwang Soo CHA
Journal of Korean Medical Science 2019;34(35):e242-
The present erratum notice corrects one figure of the article.

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