1.Validation of the finger counting method using the Monte Carlo simulation.
Hyunsu KANG ; Youngsuk CHO ; Jinhyuck LEE ; Hyunmin CHA ; Hyunjung LEE ; Daehee CHOI ; Gyu Chong CHO ; Dongkeon LEE ; Ji Yun AHN ; Youdong SOHN
Pediatric Emergency Medicine Journal 2017;4(2):58-66
PURPOSE: The dose of drug and the size of instrument are determined based on children's weight. We aimed to validate the finger counting method (FCM) for weight estimation in Korean children using the Monte Carlo simulation. METHODS: We estimated the weight of Korean children aged 1 to 9 years by the FCM. These measurements were compared with the weight extracted by the Monte Carlo simulation applied to the “2007 Korean Children and Adolescents Growth Standard”. Pearson correlation coefficients (r) were measured to assess the correlation between the weight extracted by the simulation and that estimated by FCM. Bland-Altman analyses were performed to assess the agreement between the weight extracted by the simulation and that estimated by FCM and 2 other well-known pediatric weight estimation formulas (the Advanced Pediatric Life Support and Luscombe formulas). RESULTS: Data regarding 9,000 children's weight selected by age and gender was randomly extracted using the simulation. We found a positive correlation between the weight estimated by the FCM and the weight extracted (in boys, r = 0.896, P < 0.001; in girls, r = 0.899, P < 0.001). The FCM tended to underestimate weight in the children aged 7 years or old. CONCLUSION: This article suggests the usefulness of FCM in weight estimation, particularly in children younger than 7 years. With appreciation of the limitation in older children, the FCM could be applied to emergency practice.
Adolescent
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Body Weight
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Child
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Emergencies
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Emergency Service, Hospital
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Female
;
Fingers*
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Humans
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Methods*
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Monte Carlo Method
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Resuscitation
2.Development of Models for Regional Cardiac Surgery Centers.
Choon Seon PARK ; Nam Hee PARK ; Sung Bo SIM ; Sang Cheol YUN ; Hye Mi AHN ; Myunghwa KIM ; Ji Suk CHOI ; Myo Jeong KIM ; Hyunsu KIM ; Hyun Keun CHEE ; Sanggi OH ; Shinkwang KANG ; Sok Goo LEE ; Jun Ho SHIN ; Keonyeop KIM ; Kun Sei LEE
The Korean Journal of Thoracic and Cardiovascular Surgery 2016;49(Suppl 1):S28-S36
BACKGROUND: This study aimed to develop the models for regional cardiac surgery centers, which take regional characteristics into consideration, as a policy measure that could alleviate the concentration of cardiac surgery in the metropolitan area and enhance the accessibility for patients who reside in the regions. METHODS: To develop the models and set standards for the necessary personnel and facilities for the initial management plan, we held workshops, debates, and conference meetings with various experts. RESULTS: After partitioning the plan into two parts (the operational autonomy and the functional comprehensiveness), three models were developed: the ‘independent regional cardiac surgery center’ model, the ‘satellite cardiac surgery center within hospitals’ model, and the ‘extended cardiac surgery department within hospitals’ model. Proposals on personnel and facility management for each of the models were also presented. A regional cardiac surgery center model that could be applied to each treatment area was proposed, which was developed based on the anticipated demand for cardiac surgery. The independent model or the satellite model was proposed for Chungcheong, Jeolla, North Gyeongsang, and South Gyeongsang area, where more than 500 cardiac surgeries are performed annually. The extended model was proposed as most effective for the Gangwon and Jeju area, where more than 200 cardiac surgeries are performed annually. CONCLUSION: The operation of regional cardiac surgery centers with high caliber professionals and quality resources such as optimal equipment and facility size, should enhance regional healthcare accessibility and the quality of cardiac surgery in South Korea.
Delivery of Health Care
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Education
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Gangwon-do
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Health Facilities
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Health Services Accessibility
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Humans
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Korea
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Quality of Health Care
;
Thoracic Surgery*
3.Induction of Angiogenesis by Malarial Infection through Hypoxia Dependent Manner
Mi Kyung PARK ; Eun Ji KO ; Kyung Yoon JEON ; Hyunsu KIM ; Jin Ok JO ; Kyung Wan BAEK ; Yun Jeong KANG ; Yung Hyun CHOI ; Yeonchul HONG ; Mee Sun OCK ; Hee Jae CHA
The Korean Journal of Parasitology 2019;57(2):117-125
Malarial infection induces tissue hypoxia in the host through destruction of red blood cells. Tissue hypoxia in malarial infection may increase the activity of HIF1α through an intracellular oxygen-sensing pathway. Activation of HIF1α may also induce vascular endothelial growth factor (VEGF) to trigger angiogenesis. To investigate whether malarial infection actually generates hypoxia-induced angiogenesis, we analyzed severity of hypoxia, the expression of hypoxia-related angiogenic factors, and numbers of blood vessels in various tissues infected with Plasmodium berghei. Infection in mice was performed by intraperitoneal injection of 2×10⁶ parasitized red blood cells. After infection, we studied parasitemia and survival. We analyzed hypoxia, numbers of blood vessels, and expression of hypoxia-related angiogenic factors including VEGF and HIF1α. We used Western blot, immunofluorescence, and immunohistochemistry to analyze various tissues from Plasmodium berghei-infected mice. In malaria-infected mice, parasitemia was increased over the duration of infection and directly associated with mortality rate. Expression of VEGF and HIF1α increased with the parasitemia in various tissues. Additionally, numbers of blood vessels significantly increased in each tissue type of the malaria-infected group compared to the uninfected control group. These results suggest that malarial infection in mice activates hypoxia-induced angiogenesis by stimulation of HIF1α and VEGF in various tissues.
Angiogenesis Inducing Agents
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Animals
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Anoxia
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Blood Vessels
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Blotting, Western
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Erythrocytes
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Fluorescent Antibody Technique
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Immunohistochemistry
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Injections, Intraperitoneal
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Malaria
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Mice
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Mortality
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Parasitemia
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Plasmodium
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Plasmodium berghei
;
Vascular Endothelial Growth Factor A