1.Dizziness in Patients With Obstructive Sleep Apnea
Jae Rim KIM ; Soo Ryun PARK ; Hea Ree PARK ; Eun Yeon JOO
Journal of Sleep Medicine 2022;19(2):39-45
Obstructive sleep apnea (OSA) and dizziness are common conditions observed in the general population, and several epidemiological studies have reported an association between OSA and dizziness. Vestibular dysfunction, autonomic instability, and cerebellar degeneration secondary to recurrent hypoxia are implicated as mechanisms underlying dizziness in patients with OSA. Moreover, OSA is a risk factor for many diseases associated with dizziness, including Meniere disease, stroke, and psychiatric conditions. A dizziness questionnaire, vestibular function tests, and tests for autonomic function are useful for evaluation of OSA and concomitant dizziness. A growing body of evidence has shown that effective treatment of OSA including continuous positive airway pressure therapy reduces dizziness in these patients. Greater attention to dizziness is warranted in patients with OSA.
2.Severe Cutaneous Adverse Reactions in Korean Pediatric Patients: A Study From the Korea SCAR Registry
Hea Lin OH ; Dong Yoon KANG ; Hye Ryun KANG ; Sujeong KIM ; Young Il KOH ; Sae Hoon KIM ; Min Hye KIM ; Dong In SUH ;
Allergy, Asthma & Immunology Research 2019;11(2):241-253
PURPOSE: Although severe cutaneous adverse drug reactions (SCARs) are rare, they are associated with high morbidity and mortality, and thus early diagnosis and treatment are critical for improving prognoses. However, few studies have reported the characteristics of SCARs in children. Thus, we aimed to evaluate the clinical characteristics, current management and prognosis of pediatric SCARs. METHODS: We analyzed pediatric data in the Korean SCARs registry, which was built retrospectively in 2016 with SCAR cases treated in 34 tertiary referral university hospitals during 2010–2015. Using these cases, we descriptively analyzed detailed data regarding etiology, clinical and laboratory features, treatment strategies, and prognosis. RESULTS: Forty-seven pediatric SCAR cases from 15 tertiary referral hospitals were included. The median patient age was 10 (interquartile range, 3-15.5) years and 68.1% (n = 32) were males. The culprit drug was identified in 95.7% (n = 45) of the patients; antibiotics (44.7%) and antiepileptic drugs (19.1%) were the most common and second most common culprits, respectively. Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS) cases presented with the largest area of skin involvement without permanent sequelae. Stevens-Johnson syndrome (SJS) cases involved relatively small areas of skin but serious sequelae in two children. Of 4 patients with toxic epidermal necrolysis (TEN), 1 died. Of all patients assessed, 36 (76.6%) received systemic steroids and 21 (44.7%) received intravenous immunoglobulin (IVIG). Thirteen (27.7%) received both systemic steroids and IVIG. Cyclosporine was administered to only 1 patient along with a systemic steroid. CONCLUSIONS: In patients with pediatric SCARs, including those with DRESS, SJS and TEN, clinical presentations were variable. Thus, there was no clear continuous disease spectrum. Although the mortality rate was low (2.1%), clinical suspicion may be the best tool for proactive SCAR management.
Anti-Bacterial Agents
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Anticonvulsants
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Child
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Cicatrix
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Cyclosporine
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Drug Eruptions
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Drug Hypersensitivity Syndrome
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Drug-Related Side Effects and Adverse Reactions
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Early Diagnosis
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Hospitals, University
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Humans
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Immunoglobulins
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Immunoglobulins, Intravenous
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Korea
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Male
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Mortality
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Prognosis
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Referral and Consultation
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Retrospective Studies
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Skin
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Steroids
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Stevens-Johnson Syndrome
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Tertiary Care Centers
3.Review of regulatory management on standards and specifications for veterinary medical devices in Korea.
Kyoung Mook KANG ; Tae Won KIM ; Oh Ryun KWON ; Hea Jung PARK ; Soo Min CHO ; Chung Hyun KIM ; Myoung Heon LEE ; Jin San MOON
Korean Journal of Veterinary Research 2017;57(2):71-78
Well-established standards and specifications for medical devices not only provide clarity and consistency in licensing processes but also secure device safety and effectiveness. This study reviewed regulatory standards and specifications for veterinary medical devices in Korea based on data obtained through analyses of those medical devices. General standards for electromechanical, electromagnetic, and biological safety and individual standards for 76 electric and 70 general medical device products have been established by the Korean Ministry of Food and Drug Safety. However, the first standards and specifications for veterinary medical devices were established in March 2000 for two products (disposable needle and syringe). Similar to the large number of standards for medical devices, there have been general standards for safety and individual standards for 72 veterinary medical devices (27 electric medical devices, 12 non-electric medical devices, 10 medical supplies, and 23 other types) established since 2014. These new standards considered, among other aspects, the devices' applications, usage characteristics, and industrial environment. To date, the establishment of standards and specifications for veterinary medical devices remains limited. This study suggests that improvements should be made to the regulation of general and individual standards associated with various veterinary medical instruments, supplies, and in vitro diagnostic medical reagents.
Equipment and Supplies
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Equipment Safety
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In Vitro Techniques
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Indicators and Reagents
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Korea*
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Licensure
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Magnets
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Needles
4.Enzyme-linked immunosorbent assay for detecting anti-pertussis toxin antibody in mouse.
Gi Sub CHOI ; Dong Ho HUH ; Seung Beom HAN ; Dong Ho AHN ; Kyu Ri KANG ; Ji Ahn KIM ; Bo Mi CHOI ; Hea Ryun KIM ; Jin Han KANG
Clinical and Experimental Vaccine Research 2019;8(1):64-69
PURPOSE: Although the DTaP and Tdap vaccines used to prevent pertussis have been used for a long time, there is no standard method for measuring pertussis antigens. Therefore, this preliminary study was conducted to develop an enzyme-linked immunosorbent assay method using an animal model for measuring antibodies against pertussis toxin, the most important pertussis pathogenic antigen, in the sera of vaccinated mice. MATERIALS AND METHODS: Bordetella pertussis Tohama phase I was cultured for 24–30 hours, and then pertussis toxin was purified from the culture medium by chromatography. Purified pertussis toxin was diluted in phosphate-buffered saline-coating buffer, and 100 µL of diluted pertussis toxin was added to each well and reacted at room temperature for 4 hours. Positive serum was diluted to 1/1,250–1/80,000 and negative serum was diluted to 1/50 to determine the coating concentration with the optimal signal/noise ratio. Optimal test conditions were confirmed from the dilution factors of the secondary antibody and streptavidin horseradish peroxidase (SA-HRP). RESULTS: Optimal conditions were as follows: 4 µg/mL for coating antigen; 1/40,000 for secondary antibody; and 1/1,000 for the SA-HRP dilution factor. Comparison of the sera obtained from mice treated with a developing vaccine and commercial vaccine with National Institute for Biological Standard and Control standard serum under the established conditions showed the following results: 1,300.62, 534.94, and 34.85, respectively. CONCLUSION: The method developed in this study is suitable for measuring anti-pertussis toxin antibodies and may be applicable for clinical sample analysis or indirect diagnosis of pertussis.
Animals
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Antibodies
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Bordetella pertussis
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Chromatography
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Diagnosis
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Enzyme-Linked Immunosorbent Assay*
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Horseradish Peroxidase
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Methods
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Mice*
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Models, Animal
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Pertussis Toxin
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Streptavidin
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Vaccines
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Whooping Cough
5.Cytogenetic Analysis of Amniotic Fluid, CVS, and Abortus in a University Hospital for Ten Years.
Sook Hyang CHOI ; Jeong Yeal AHN ; Kyung Hee KIM ; Hye Ryun YANG ; Yang Hee LEE ; Myoung Suk YOO ; Han Ik SUH ; Pil Whan PARK ; Yiel Hea SEO
Journal of Laboratory Medicine and Quality Assurance 2009;31(2):293-299
BACKGROUND: This study was conducted to analyze, compare, and assess the indications, incidences, and types of chromosomal abnormalities in the amniotic fluid, chorionic villus sampling (CVS), and abortus and to compare these with those previously reported. METHODS: The study subjects included 1,995 cases of amniocentesis and 169 cases of abortus, 20 cases of CVS, 21 cases of cord blood, and 2 cases of cardiac-puncture fluid in the last ten years (June 1999 to May 2009). RESULTS: Among the indications, the maternal serum and triple/quad markers testing positive emerged the highest (57.5%). Other factors those were found were an advanced maternal age (over35) (19.5%) and abnormal ultrasonography findings (8.2%). The frequency of chromosomal abnormality in the amniotic fluid was 4.5%, wherein the numerical abnormality was 3.1% and the structural abnormality was 1.4%. Among the numerical abnormalities, trisomy of chromosome 21 emerged the highest (1.4%). The frequency of the chromosomal abnormality of CVS and abortus was 39.1%, the numerical abnormality was 23.7%, and the order of frequency for trisomy was obtained chromosomes 16, 22, and 21. In the sex ratio of the normal chromosomes, it was 1.1%, but it resulted in 0.5% in CVS. CONCLUSIONS: The results of this chromosomal study on amniotic fluid, CVS, and abortus could serve as useful data regarding the prenatal genetic abnormalities of fetuses and for genetic consultation.
Amniocentesis
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Amniotic Fluid
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Chorionic Villi Sampling
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Chromosome Aberrations
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Chromosomes, Human, Pair 21
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Cytogenetic Analysis
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Cytogenetics
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Female
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Fetal Blood
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Fetus
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Incidence
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Maternal Age
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Pregnancy
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Sex Ratio
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Trisomy