1.Risk Factors of Outcomes of COVID-19 Patients in Korea: Focus on Early Symptoms
Su Yeon JANG ; Jeong-Yeon SEON ; Baik-Lin EUN ; Seong-Beom KOH ; Jin-Hong YOO ; Woo Yong LEE ; Ho-Kee YUM ; Seok-Jun YOON ; In-Hwan OH ; Sang-Cheol BAE ; Sung-Goo CHANG
Journal of Korean Medical Science 2021;36(18):e132-
Background:
Coronavirus disease 2019 (COVID-19) has spread around the globe, and it is important to determine the risk factors of death in the general population. Our study aimed to determine the risk factors of death and severe illness requiring supplemental oxygen therapy based on the demographic and clinical characteristics of COVID-19 patients in Korea.
Methods:
In this study, we used data provided by the Korea Disease Control and Prevention Agency (KDCA) and analyzed a total of 5,068 patients with COVID-19, excluding 19 pregnant women and 544 individuals with missing data. We performed logistic regression analysis to determine the impact of early symptoms on survival and severe disease. Logistic regression models included sex, age, number of comorbidities, symptoms on admission, blood pressure, heart rate, and body temperature as explanatory variables, and death and oxygen therapy as outcome variables.
Results:
Logistic regression analyses revealed that the male sex, older age (≥ 60 years), higher number of comorbidities, presence of symptoms on admission, heart rate ≥ 120 bpm, and body temperature ≥ 37.5°C presented with higher risk of in-hospital death and oxygen therapy requirement. Conversely, rhinorrhea and headache were associated with a low risk of death and oxygen therapy requirement. The findings showed that cough, sputum, and fever were the most common symptoms on admission, while 25.3% of patients with COVID-19 were asymptomatic.
Conclusion
COVID-19 patients with high-risk early symptoms on admission, such as dyspnea and altered mental status, and those without low-risk symptoms of rhinorrhea and headache should be included in priority treatment groups.
2.Risk Factors of Outcomes of COVID-19 Patients in Korea: Focus on Early Symptoms
Su Yeon JANG ; Jeong-Yeon SEON ; Baik-Lin EUN ; Seong-Beom KOH ; Jin-Hong YOO ; Woo Yong LEE ; Ho-Kee YUM ; Seok-Jun YOON ; In-Hwan OH ; Sang-Cheol BAE ; Sung-Goo CHANG
Journal of Korean Medical Science 2021;36(18):e132-
Background:
Coronavirus disease 2019 (COVID-19) has spread around the globe, and it is important to determine the risk factors of death in the general population. Our study aimed to determine the risk factors of death and severe illness requiring supplemental oxygen therapy based on the demographic and clinical characteristics of COVID-19 patients in Korea.
Methods:
In this study, we used data provided by the Korea Disease Control and Prevention Agency (KDCA) and analyzed a total of 5,068 patients with COVID-19, excluding 19 pregnant women and 544 individuals with missing data. We performed logistic regression analysis to determine the impact of early symptoms on survival and severe disease. Logistic regression models included sex, age, number of comorbidities, symptoms on admission, blood pressure, heart rate, and body temperature as explanatory variables, and death and oxygen therapy as outcome variables.
Results:
Logistic regression analyses revealed that the male sex, older age (≥ 60 years), higher number of comorbidities, presence of symptoms on admission, heart rate ≥ 120 bpm, and body temperature ≥ 37.5°C presented with higher risk of in-hospital death and oxygen therapy requirement. Conversely, rhinorrhea and headache were associated with a low risk of death and oxygen therapy requirement. The findings showed that cough, sputum, and fever were the most common symptoms on admission, while 25.3% of patients with COVID-19 were asymptomatic.
Conclusion
COVID-19 patients with high-risk early symptoms on admission, such as dyspnea and altered mental status, and those without low-risk symptoms of rhinorrhea and headache should be included in priority treatment groups.
3.Fellows' perception of fellowship training and overarching issues.
Eunbae B YANG ; Sun Whe KIM ; Jae Joong KIM ; Baik Lin EUN ; Seong Taek OH ; Bong Soo CHA ; Seung Koo LEE ; Hyun Soo CHUNG ; Dong Ik KIM
Journal of the Korean Medical Association 2016;59(12):969-976
Patient expectations for specialized medical care have spawned fellowship programs that require additional subspecialty training after residency training completion. The present study assessed the curricula and training environment adequacy of fellowship programs as perceived by current trainees and identified improvement areas for South Korea's overall fellowship program. A questionnaire was distributed to 1,764 fellows training at 6 university hospitals in Seoul, Korea during October 2014. From a return rate of 33.1%, 26.2% (403 responses) of all questionnaires distributed were compete enough to include in the analysis. Fellows participating in the survey were enrolled in fellowship programs with occupational aspirations of professorship and academic aspirations of subspecialty exploration. Nevertheless, more than half of the participating fellows did not have a clear understanding of their program's objectives. Many hoped for reduced clinical hours, increased research time allowance, and higher pay compared to current training environment and salary. The fellows' satisfaction with their program's curriculum and training environment was above 3 points on a Likert scale of 1 to 5. Receiving a training objective and financial support for academic activities by the training institution were factors influencing fellows' satisfaction level regarding both the curriculum and training environment. Clearly defined program objectives, a specialized curriculum for fellows, improved working conditions, and reflection on medical workforce policies are imperative for the advancement of Korean fellowship programs.
Aspirations (Psychology)
;
Curriculum
;
Fellowships and Scholarships*
;
Financial Support
;
Hope
;
Hospitals, University
;
Humans
;
Internship and Residency
;
Korea
;
Personal Satisfaction
;
Salaries and Fringe Benefits
;
Seoul
4.Single-center experience of the Korean-Developmental Screening Test for infants and children.
Chae Ri SUH ; Su Ye SOHN ; Gun Ha KIM ; Seong Kwan JUNG ; Baik Lin EUN
Korean Journal of Pediatrics 2016;59(12):483-489
PURPOSE: We investigated the number of test takers of the Korean-Developmental Screening Test (K-DST) in a single children's hospital within a year, according to age, referral rate, and follow-up percentage. METHODS: For this study, 4,062 children who visited and received K-DST at Woorisoa Children's Hospital between January and December 2015 were enrolled. Seven test sets were used according to the Korean National Health Screening Program for infants and children in the following age groups: 4 to 6, 9 to 12, 18 to 24, 30 to 36, 42 to 48, 54 to 60, and 66 to 71 months. The results of the K-DST were categorized into 4 groups as follows: further evaluation (<−2 standard deviation [−2SD]), follow-up test (−2SD to −1SD), peer level (−1SD to 1SD), and high level (>1SD). RESULTS: The test participants' population and follow-up population were concentrated before the age of 24 months (2,532, 62.3%). The children most commonly referred for further evaluation were those in the 30- to 41-month age group. A mismatch was found between the results of the K-DST and the additional questions. Most of the infants and children with suspicious developmental delays showed catch-up development in their follow-up tests (43 of 55, 78.2%). CONCLUSION: The use of K-DST should be encouraged, especially among children aged over 24 months. Multiple-choice question format for the additional questions is recommended to avoid confusion. We suggest a nationwide study to evaluate and revise the K-DST.
Child*
;
Follow-Up Studies
;
Humans
;
Infant*
;
Korea
;
Mass Screening*
;
Referral and Consultation
5.Biochemical and Genetic Analysis of Seven Korean Individuals With Suspected Metachromatic Leukodystrophy.
Minje HAN ; Sun Hee JUN ; Yun Jin LEE ; Baik Lin EUN ; Seung Jun LEE ; Moon Woo SEONG ; Sung Sup PARK ; Sang Hoon SONG ; Hyung Doo PARK ; Junghan SONG
Annals of Laboratory Medicine 2015;35(4):458-462
Metachromatic leukodystrophy (MLD) is an autosomal recessive disease caused by a deficiency in arylsulfatase A (ARSA). However, decreased ARSA activity is also observed in pseudodeficiency (PD). To distinguish between MLD and PD, we performed gene mutation and sulfatide analyses by using dried blood spots (DBSs) from seven Korean individuals who underwent an analysis of ARSA activity. DNA was extracted from DBSs, and PCR-direct sequencing of ARSA was performed. The cDNA obtained was analyzed to confirm a novel mutation. Of the seven subjects, three were confirmed as having MLD, one was confirmed as having MLD-PD, one was confirmed as having PD, and the remaining two were obligate heterozygotes. We verified the novel pathogenic variant c.1107+1delG by performing familial and cDNA analyses. Sulfatide concentrations in DBSs were analyzed and were quantified by using ultra-performance liquid chromatography and tandem mass spectrometry, respectively. Total sulfatide concentration was inversely correlated with ARSA activity (Spearman's coefficient of rank correlation, P=0.929, P=0.0025). The results of this mutational and biochemical study on MLD will increase our understanding of the genetic characteristics of MLD in Koreans.
Cerebroside-Sulfatase
;
Chromatography, Liquid
;
DNA
;
DNA, Complementary
;
Heterozygote
;
Leukodystrophy, Metachromatic*
;
Tandem Mass Spectrometry
6.Cross-Protective Immune Responses Elicited by Live Attenuated Influenza Vaccines.
Yonsei Medical Journal 2013;54(2):271-282
The desired effect of vaccination is to elicit protective immune responses against infection with pathogenic agents. An inactivated influenza vaccine is able to induce the neutralizing antibodies directed primarily against two surface antigens, hemagglutinin and neuraminidase. These two antigens undergo frequent antigenic drift and hence necessitate the annual update of a new vaccine strain. Besides the antigenic drift, the unpredictable emergence of the pandemic influenza strain, as seen in the 2009 pandemic H1N1, underscores the development of a new influenza vaccine that elicits broadly protective immunity against the diverse influenza strains. Cold-adapted live attenuated influenza vaccines (CAIVs) are advocated as a more appropriate strategy for cross-protection than inactivated vaccines and extensive studies have been conducted to address the issues in animal models. Here, we briefly describe experimental and clinical evidence for cross-protection by the CAIVs against antigenically distant strains and discuss possible explanations for cross-protective immune responses afforded by CAIVs. Potential barriers to the achievement of a universal influenza vaccine are also discussed, which will provide useful guidelines for future research on designing an ideal influenza vaccine with broad protection without causing pathogenic effects such as autoimmunity or attrition of protective immunity against homologous infection.
Adaptive Immunity
;
Antigens, Viral/immunology
;
*Cross Protection
;
Genome, Viral
;
Humans
;
Immunity, Innate
;
Influenza Vaccines/*immunology/therapeutic use
;
Influenza, Human/*prevention & control
;
Orthomyxoviridae/genetics/immunology
;
Vaccines, Attenuated
7.Toward a universal influenza vaccine: from the perspective of protective efficacy.
Clinical and Experimental Vaccine Research 2013;2(2):71-73
No abstract available.
Collodion
;
Influenza, Human
8.Recombinant influenza viruses as delivery vectors for hepatis B virus epitopes.
Jae Min SONG ; Kwang Hee LEE ; Baik Lin SEONG
Clinical and Experimental Vaccine Research 2012;1(1):77-82
PURPOSE: Neuraminidase (NA) of influenza virus contains stalk region that shows a great deal of variability in both amino acid sequence and length. In this paper, we investigated generation of recombinant influenza viruses that had hepatitis B virus (HBV) B cell epitopes in the NA stalk region as a dual vaccine candidate. MATERIALS AND METHODS: We used the WSH-HK reassortant helper virus for rescue of recombinant influenza virus containing HBV epitopes and reverse genetic protocol based on the use of micrococcal nuclease-treated virus cores for reconstitution of ribonucleoproteins. RESULTS: We successfully generated a chimeric influenza viruses which contained 22 amino acid peptides in the stalk region derived from the surface and pre-surface protein HBV. The growth kinetics of the recombinant viruses was investigated after infection of Madin-Darby canine kidney (MDCK) and Madin-Darby bovine kidney (MDBK) cells and the rIV-BVPreS virus showed higher titer than other viruses in MDCK cells. We also confirmed the presence of HBV epitopes in the chimeric viruses by enzyme-linked immunosorbent assay (ELISA) using anti-HBV polyclonal antibody. When the ratio of recombinant virus verse wild type virus was calculated by ELISA, recombinant viruses exhibited 2 fold higher values than the wild type virus. CONCLUSION: These results suggest that chimeric influenza virus which contained foreign antigens can be used as dual vaccine against both HBV and influenza viruses.
Amino Acid Sequence
;
Enzyme-Linked Immunosorbent Assay
;
Epitopes
;
Epitopes, B-Lymphocyte
;
Helper Viruses
;
Hepatitis B virus
;
Herpesvirus 1, Cercopithecine
;
Influenza, Human
;
Kidney
;
Kinetics
;
Madin Darby Canine Kidney Cells
;
Neuraminidase
;
Orthomyxoviridae
;
Peptides
;
Viruses
9.Principles underlying rational design of live attenuated influenza vaccines.
Clinical and Experimental Vaccine Research 2012;1(1):35-49
Despite recent innovative advances in molecular virology and the developments of vaccines, influenza virus remains a serious burden for human health. Vaccination has been considered a primary countermeasure for prevention of influenza infection. Live attenuated influenza vaccines (LAIVs) are particularly attracting attention as an effective strategy due to several advantages over inactivated vaccines. Cold-adaptation, as a classical means for attenuating viral virulence, has been successfully used for generating safe and effective donor strains of LAIVs against seasonal epidemics and occasional pandemics. Recently, the advent of reverse genetics technique expedited a variety of rational strategies to broaden the pool of LAIVs. Considering the breadth of antigenic diversity of influenza virus, the pool of LAIVs is likely to equip us with better options for controlling influenza pandemics. With a brief reflection on classical attenuating strategies used at the initial stage of development of LAIVs, especially on the principles underlying the development of cold-adapted LAIVs, we further discuss and outline other attenuation strategies especially with respect to the rationales for attenuation, and their practicality for mass production. Finally, we propose important considerations for a rational vaccine design, which will provide us with practical guidelines for improving the safety and effectiveness of LAIVs.
Antigenic Variation
;
Cross Protection
;
Humans
;
Influenza Vaccines
;
Influenza, Human
;
Orthomyxoviridae
;
Pandemics
;
Reverse Genetics
;
Seasons
;
Tissue Donors
;
Vaccination
;
Vaccines, Inactivated
10.Reverse genetic platform for inactivated and live-attenuated influenza vaccine.
Eun Ju JUNG ; Kwang Hee LEE ; Baik Lin SEONG
Experimental & Molecular Medicine 2010;42(2):116-121
Influenza vaccine strains have been traditionally developed by annual reassortment between vaccine donor strain and the epidemic virulent strains. The classical method requires screening and genotyping of the vaccine strain among various reassortant viruses, which are usually laborious and time-consuming. Here we developed an efficient reverse genetic system to generate the 6:2 reassortant vaccine virus from cDNAs derived from the influenza RNAs. Thus, cDNAs of the two RNAs coding for surface antigens, haemagglutinin and neuraminidase from the epidemic virus and the 6 internal genes from the donor strain were transfected into cells and the infectious viruses of 6:2 defined RNA ratio were rescued. X-31 virus (a high-growth virus in embryonated eggs) and its cold-adapted strain X-31 ca were judiciously chosen as donor strains for the generation of inactivated vaccine and live-attenuated vaccine, respectively. The growth properties of these recombinant viruses in embryonated chicken eggs and MDCK cell were indistinguishable as compared to those generated by classical reassortment process. Based on the reverse genetic system, we generated 6 + 2 reassortant avian influenza vaccine strains corresponding to the A/Chicken/Korea/MS96 (H9N2) and A/Indonesia/5/2005 (H5N1). The results would serve as technical platform for the generation of both injectable inactivated vaccine and the nasal spray live attenuated vaccine for the prevention of influenza epidemics and pandemics.
Animals
;
Chick Embryo
;
Chickens
;
Genetic Engineering
;
Hemagglutinins, Viral/genetics/metabolism
;
Humans
;
Influenza A Virus, H5N1 Subtype/*genetics/immunology
;
Influenza A Virus, H9N2 Subtype/*genetics/immunology
;
Influenza Vaccines/*genetics/metabolism
;
Influenza in Birds/immunology/virology
;
Influenza, Human/immunology/*prevention & control/virology
;
Neuraminidase/genetics/metabolism
;
Transgenes
;
Vaccines, Attenuated/*genetics/metabolism
;
Viral Proteins/genetics/metabolism

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