1.Crescentic Glomerulonephritis in a Patient with Rheumatoid Arthritis: A case report.
Ki Ouk MIN ; Yeong Jin CHOI ; Byoung Kee KIM ; Sun Moo KIM ; Sang In SHIM
Korean Journal of Pathology 1995;29(1):116-118
Crescentic glomerulonephritis in rheumatoid arthritis is described recently with increasing frequency. It can occur directly as a manifestation of rheumatoid arthritis or may be a reaction to drugs such as D-penicillamine and bucillamine. We report a case of crescentic glomerulonephritis in a 46-year-old woman with rheumatoid arthritis for 20 years who had been treated intermittently with herb medicine or nonsteroidal anti-inflammatory drugs (NSAIDS). Light microscopic examination showed severe focal segmental and global necrotizing glomerulonephritis with crescent formation in 50% of the glomeruli. Immunofluorescent study revealed scanty amount of mesangial granular deposits of IgA, IgM, C3 and fibrinogen in a diffuse pattern.
Female
;
Humans
2.Treatment with EMA-CO regimen in the management of high risk gestational trophoblastic tumor.
Young Min CHOI ; Jin Wan PARK ; Do Yeong HWANG ; Soon Beom KANG ; Hyo Pyo LEE
Korean Journal of Obstetrics and Gynecology 1991;34(1):91-100
No abstract available.
Trophoblastic Neoplasms*
;
Trophoblasts*
3.Usefulness of HhaI and MseI DNA Polymorphism of Factor IX Gene in the Molecular Genetic Diagnosis of Hemophilia B in Korean Population.
Jae Hak LEE ; Young Min CHOI ; Jin CHOE ; Do Yeong HWANG ; Jin Yong LEE
Korean Journal of Obstetrics and Gynecology 1999;42(12):2761-2767
OBJECTIVES: Hemophilia B has been known to result from more than 500 kinds of mutations. And it is difficult to find out a mutation specific for each family. Therefore, linkage analysis of DNA polymorphism within or near the factor IX gene has been frequently used in the clinical practice for molecular genetic diagnosis of hemophilia B. But the ethnic variation makes more difficult to apply useful markers in Caucasian population. To investigate the usefulness of the MseI and HhaI polymorphism in Korean population, we analysed the MseI and HhaI polymorphism. METHODS: Forty-five normal Korean and thirteen parents of the hemophilia B patients, using PCR and restriction enzyme analysis. RESULTS: The heterozygosity rate of MseI polymorphism was 49.7% and that of HhaI polymorphism was 25.5%. CONCLUSION: These data indicated that PCR-based analysis of MseI and HhaI polymorphism of factor IX was useful in molecular genetic diagnosis of hemophilia B in Korean population.
Diagnosis*
;
DNA*
;
Factor IX*
;
Hemophilia A*
;
Hemophilia B*
;
Humans
;
Molecular Biology*
;
Parents
;
Polymerase Chain Reaction
;
Prenatal Diagnosis
;
Restriction Mapping
4.Factors Influencing the Infection Control Performance of Catheter-Associated Urinary Tract Infection of Nurses in Hospitals
Journal of Korean Clinical Nursing Research 2019;25(3):303-313
PURPOSE:
The purpose of this study was to examine nurses' knowledge, health beliefs, and performance regarding the infection control of catheter-associated urinary tract infection (CAUTI) and to identify factors affecting their infection control performance of the CAUTI.
METHODS:
The subjects were 166 nurses at three hospitals with less than 300 beds in urban areas.Data were collected using structured questionnaires about knowledge, health beliefs, and performance regarding the infection control of the CAUTI. Statistical analysis included t-test, ANOVA, Pearson's Correlation Coefficients, Multiple regression analysis.
RESULTS:
The factors affecting the infection control performance of CAUTI were knowledge (β=.18, p=.010), perceived seriousness (β=.25, p=.001), perceived barriers (β=.41, p<.001), and cues to action (β=.15, p=.030), and these factors explained 28.7% of the variance for the infection control performance of the CAUTI.
CONCLUSION
In this study, higher levels of knowledge, perceived seriousness and, cues to action, and lower perceived barriers resulted in a corresponding higher performance in the infection control of CAUTI. Based on these findings, providing intervention programs enhancing the health beliefs of nurses is necessary to ensure their infection control performance of the CAUTI.
5.Bupivacaine-lidocaine versus Ropivacaine-lidocaine Retrobulbar Anesthesia in Vitreoretinal Surgery
Yeong A CHOI ; Areum JEONG ; Min SAGONG
Journal of the Korean Ophthalmological Society 2021;62(12):1600-1606
Purpose:
To compare efficacies of bupivacaine-lidocaine and ropivacaine-lidocaine mixtures in terms of inducing retrobulbar anesthesia during vitrectomy.
Methods:
Sixty patients who underwent retrobulbar anesthesia during vitrectomy were divided into two groups. Patients in group 1 received a mixture of bupivacaine and lidocaine (n = 30); patients in group 2 received a mixture of ropivacaine and lidocaine (n = 30). The effects of the two combinations were retrospectively compared and analyzed. The onset times of analgesia and akinesia were measured. Two hours after surgery, sensory blockade was assessed by touching the corneas with cotton swabs and by communicating with patients. Ocular movement was evaluated in four gaze direction quadrants. A 10-point visual analog pain scale was used to assess pain during and 2 hours after surgery. Intra- and postoperative complications were recorded.
Results:
The mean analgesia onset times in groups 1 and 2 were 94.62 ± 28.87 and 92.32 ± 35.53 seconds, respectively (p = 0.071); the mean akinesia onset times were 147.89 ± 59.35 and 132.57 ± 76.38 seconds (p = 0.223), respectively. Patients in group 2 reported significantly less postoperative pain and exhibited less postoperative ocular movement, compared with patients in group 1 (both p = 0.002). One patient in group 1 experienced respiratory depression after retrobulbar blockade.
Conclusions
When retrobulbar anesthesia is required during vitrectomy, a ropivacaine-lidocaine mixture and a bupivacaine-lidocaine mixture induce anesthesia with similar rapidity. However, the ropivacaine-lidocaine mixture is safer and affords better-quality intra- and postoperative anesthesia.
6.Spontaneous abortion and recurrent miscarriage: A comparison of cytogenetic diagnosis in 250 cases.
Tae Yeong CHOI ; Hye Min LEE ; Won Kyoung PARK ; So Yeong JEONG ; Hwa Sook MOON
Obstetrics & Gynecology Science 2014;57(6):518-525
OBJECTIVE: The purpose of this study was to determine the frequency and distribution of cytogenetically abnormal miscarriages in couples with spontaneous abortions (SA) or recurrent miscarriages (RM). METHODS: Karyotyping of specimens from 164 abortuses with SA and 86 abortuses with RM was successfully performed according to the standard cytogenetic methods using G-banding technique. RESULTS: Among the total 164 cases of SA group, 81 (49.4%) were euploid and the rest (83, 50.6%) showed chromosomal abnormalities. In RM(> or =2) and RM(> or =3) group, 31 (36.0%)/27 (34.6%) cases were euploid and 55 (64.0%)/51(65.4%) cases were abnormal, respectively. A statistically significant difference was found in the rate of cytogenetic abnormality between SA and RM groups (P<0.05). In all groups, women with advanced maternal age (> or =35 years) had a higher rate of chromosome anomalies compared with women younger than age 35 (normal:abnormal = 32.4%:67.6% for > or =35 years and 53.8%:46.2% for <35 years in SA; 19.2%:80.8%/21.7%:78.3% for > or =35 years and 43.3%:56.7%/40.0%:60.0% for <35 years in RM(> or =2) and RM(> or =3), respectively; P<0.05). In SA group, an increase of normal karyotypes was noted with increased gestational age (<10 week, 38.0%; 10-15 week, 53.5%; 16-20 week, 65.7%). In RM group, most of cases were in <10 week and the frequency of trisomies with chromosomes 1 to 10 were increased compared with that of SA. CONCLUSION: There was a statistically significant difference in the frequency and distribution of chromosomal abnormalities between SA and RM groups. Our results will provide useful information for diagnosis and genetic counseling of patients with SA or RM.
Abortion, Habitual*
;
Abortion, Spontaneous*
;
Chromosome Aberrations
;
Cytogenetic Analysis
;
Cytogenetics*
;
Diagnosis*
;
Family Characteristics
;
Female
;
Genetic Counseling
;
Gestational Age
;
Humans
;
Karyotype
;
Karyotyping
;
Maternal Age
;
Pregnancy
;
Trisomy
7.Detection of Down Syndrome & Edward Syndrome in uncultured amniocytes using FISH ( Fluorescence In Situ Hybridization.
Shin Yong MOON ; Jin CHOI ; Do Yeong HWANG ; Young Min CHOI ; Eun Ju CHANG ; Kyung Soon CHEONG ; Ki Chul KIM ; Eung Gi MIN ; Jin Yong LEE
Korean Journal of Obstetrics and Gynecology 1998;41(11):2859-2863
FISH is suggested as a possible method to detect the numerical and structural abnormalities of chromosomes in interphase nucleus. We performed this study to discuss the clinical usefulness of FISH in uncultured amniocytes and to set up the cut-off value for further study. We collected amniotic fluid samples from patients whose chromosome studies were recommended due to screen positive for Down and Edword syndrome in triple marker test using maternal serum. The centromeric probe for chromosome 18 and the locus-specific probe for chromosome 21 were used and the results were compared to their karyotypes. We could find 2 cases of trisony 21 and 2 cases of trisony 18 and the other cases represented normal karyotypes. The accuracies were 91% for disomy 18, 89% for trisomy 18, 92% for disomy 21 and 88% for trisomy 21. Therefore FISH technique is a possible method to detect the chromosomal abnormalities in uncultured amniocytes and the use of locus-specific probe for chromosome 21 would be more useful for detecting the aneuploidy of chromosome 21 than 13/21 centromeric probe.
Amniotic Fluid
;
Aneuploidy
;
Chromosome Aberrations
;
Chromosomes, Human, Pair 18
;
Chromosomes, Human, Pair 21
;
Down Syndrome*
;
Female
;
Fluorescence*
;
Humans
;
In Situ Hybridization*
;
In Situ Hybridization, Fluorescence
;
Interphase
;
Karyotype
;
Trisomy
8.Multicenter Trial of Aberrations of Chromosomes in Abortuses, Chorionic villi, Amniocytes, and Fetal Blood Cells.
Jong Kwan JUN ; Jin CHOE ; Young Min CHOI ; Do Yeong HWANG ; Sun Kyung OH ; Shin Yong MOON ; Jin Yong LEE
Korean Journal of Obstetrics and Gynecology 2000;43(7):1200-1206
OBJECTIVES: Chromosomal anomalies are common disease entity among genetic diseases. But there are scanty reports about the status of chromosomal abnormalities in Korean. In addition, the comprehensive multi-center study of chromosomal abnormalities in Korean has never been performed. METHODS: We have collected 1,793 cases (394 abortuses; 198 chorionic villi; 1,060 amniotic fluid cells; 141 fetal blood), which showed abnormal karyotype results from twenty three cytogenetic centers in Korea from the year of 1977 to 1999. RESULTS: In abortuses, numerical chromosomal abnormalities was 85%, and structural abnormalities was 13% and the most frequent anomaly was trisomy 16. In chorionic villi, numerical anomaly was 60.0% and structural anomaly was 31.3% and the most frequent karyotype was Down syndrome. In amniotic fluid cells, structural anomaly exceeded the number of numerical anomaly and the most frequent anomaly was Down syndrome. In fetal blood, numerical anomaly was 63.8% and the most frequent karyotype was trisomy 18 (23.4%) CONCLUSIONS: This may be the first comprehensive and multi-center study in Korea. The proportion of the abnormal karyotypes in each specimens was different from each other. Based on this study, the more comprehensive study should be performed to all the Korean population.
Abnormal Karyotype
;
Amniotic Fluid
;
Chorion*
;
Chorionic Villi*
;
Chromosome Aberrations
;
Cytogenetics
;
Down Syndrome
;
Female
;
Fetal Blood*
;
Karyotype
;
Korea
;
Trisomy
9.Mycoplasma pneumoniae-induced Stevens-Johnson syndrome without skin manifestations.
Sun Hee CHOI ; Yu Min LEE ; Yeong Ho RHA
Korean Journal of Pediatrics 2009;52(2):247-250
Stevens-Johnson syndrome (SJS) presents with widespread blisters, erythematous or purpuric macules, and one or more mucous membrane erosions. Various etiologic factors, including infection, vaccination, drug administration, systemic diseases, physical agents, and food have been implicated as causes of SJS. Mycoplasma pneumoniae is the most common infectious agent to cause SJS in children. In recent literature, M. pneumoniae-induced SJS with mucositis that lacks the typical target lesions has been described. We report a case of a 6-year-old boy with swelling, peeling of the lips, and red eyes with photosensitivity. On physical examination, he showed severe oral mucositis and conjunctivitis with no evidence of skin lesions. Mycoplasma antibody, which was positive with titers of more than 1:2,560. For patients presenting with fever and mucositis of unknown origin, M. pneumoniae should be considered.
Blister
;
Child
;
Conjunctivitis
;
Eye
;
Fever
;
Humans
;
Lip
;
Mucositis
;
Mucous Membrane
;
Mycoplasma
;
Mycoplasma pneumoniae
;
Physical Examination
;
Pneumonia
;
Pneumonia, Mycoplasma
;
Skin
;
Skin Manifestations
;
Stevens-Johnson Syndrome
;
Stomatitis
;
Vaccination
10.Cerebral Vasoreactivity in Carotid Stenosis or Occlusion Cases: A Transcranial Doppler Study with Acetazolamide (Diamox) Test.
Seong Min PARK ; Kwang Soo LEE ; Jae Young CHOI ; Yeong In KIM
Journal of the Korean Neurological Association 1998;16(4):439-443
BACKGROUND: The aim of this trial was to evaluate the acetazolamide induced vasoreactivity of the cerebral vasculature in patients with carotid stenosis/occlusion, relative changes of blood flow velocity within the middle cerebral artery were measured by transcranial doppler ultrasonography during acetazolamide challenge. To evaluate the effectiveness of extracranial-intracranial bypass surgery in patients with ICA stenosis/occlusion with decreased vasoreactivity, we studied whether the vasoreactivity could show a significant difference between the territorial infarction and borderzone infarction cases. METHODS: To test vasoreactivity in 21 patients with unilateral carotid stenosis or occlusion, we measured blood flow velocity in the middle cerebral artery by transcranial doppler sonography both at rest and after injection of acetazolamide. Among 21 patients, 13 patients are MCA territorial and 8 patients are borderzone infarction which are angiographically confirmed symptomatic cases. RESULTS: The increase in blood flow velocity (%Vm) after acetazolamide stimulation was significantly different between the both hemisphere (affected side: 24.01+/-24.44%, contralateral side: 49.39+/-19.38%, p<0.05). In patients with carotid stenosis/occlusion, vasoreactivity of the borderzone infarction cases was lower than territorial infarction cases(mean+/-SD: 12.25+/-11.20% and 29.92+/-26.42%, p=0.13), but it is not significant statistically. CONCLUSION: We concluded that TCD with acetazolamide challenge is a useful method for assessment of the adequacy of hemodynamic reserve in patients with severe stenosis or occlusive cerebrovascular disease but it is very difficult problem apply to EC-IC bypass surgery directly.
Acetazolamide*
;
Blood Flow Velocity
;
Carotid Stenosis*
;
Constriction, Pathologic
;
Hemodynamics
;
Humans
;
Infarction
;
Middle Cerebral Artery
;
Ultrasonography, Doppler, Transcranial