1.Sleep Patterns and Academic Performance in Medical Students.
Seo Yeon SHIN ; Jin Seong LEE ; Do Un JEONG
Sleep Medicine and Psychophysiology 2008;15(2):87-93
INTRODUCTION: Although it is well known that medical students are not getting an adequate amount of sleep, there have been only few studies on the sleep patterns of medical students in Korea. Therefore, the present study aimed to investigate the life style and sleep patterns of Korean medical students and the impact they have on the students' academic performance. METHODS: A questionnaire package was administered to the 3rd year medical students at the Seoul National University to examine their sleep patterns on weekdays and weekends. It consisted of questions asking about their lifestyles as well as Pittsburgh sleep quality index (PSQI) and GPA (Grade Point Average) that are considered relevant to their sleep patterns. A total of 110 students (85 males and 25 females, mean age 24.4+/-20.6) responded to the survey and the result was analyzed using the independent t-test, the chi-square test, the paired t-test, Pearson's rank correlation and ANOVA. P-values of less than 0.05 were considered statistically significant in all analyses. RESULTS: The weekend bedtime was significantly delayed (01:24 on weekday; 03:12 on weekend; t=-5.23, p<0.01), the weekend rise time was delayed (07:36 on weekday; 10:30 on weekend; t=-24.48, p<0.01) and the total sleep time was increased on weekends (5:57 on weekday; 8:17 on weekend; t=15.94, p<0.01). They wished to sleep for 7 hours 6 minutes which was different from their actual weekday total sleep time (t=-11.41, p<0.01). The poor sleeper group had lower GPAs than the good sleeper group (t=2.05, p<0.05). The GPA of medical students were negatively correlated with age (r=-0.23, p<0.05), daily amount of smoking (r=-0.78, p<0.01), total amount of smoking (r=-0.75, p<0.01), weekday sleep latency (r=-0.23, p<0.05), weekend sleep latency (r=-0.23, p<0.05) and PSQI score (r=-0.30, p<0.01). CONCLUSION: Medical students were experiencing a lack of sleep during weekdays as they have a later bedtime and earlier rise time, and consequently had more hours of sleep on weekends. Overall, the responded students were experiencing poor sleep quality, and the GPAs of the poor sleeper group were lower than those of the good sleeper group.
Female
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Humans
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Korea
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Life Style
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Male
;
Surveys and Questionnaires
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Smoke
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Smoking
;
Students, Medical
2.Chronic intestinal pseudoobstruction syndrome.
Kyung Mo YEON ; Jeong Kee SEO ; Yong Seok LEE
Journal of the Korean Radiological Society 1992;28(2):287-292
Chronic intestional pseudoobstruction syndrome is a rare clinical condition in which impaired intestinal peristalsis. Causes recurrent symptoms of bowel obstruction in the absence of a mechanical occlusion. This syndrome may involve variable segments of small or large bowel. And may be associated with urinary bladder retention. This study included 6 children(3 boys and 3 girls) of chronic intestinal obstruction. Four were symptomatic at birth and two were of the ages of one month and one year. All had abdominal distention and defication difficulty. Five had urinary bladder distention. Despite parenteral nutrition and surgical intervention(ileostomy or colostomy), bowel obstruction persisted and four patients expired from sepsis within one year. All had gaseous distention of small and large bowel on abdominal films. In small bowel series. Consistent findings were variable degree of dilatation. Decreased peristalsis(prolonged transit time) and microcolon or microrectum. This disease entity must be differentiated from congenital megacolon, ileal atresia and megacystis syndrome.
Dilatation
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Hirschsprung Disease
;
Humans
;
Intestinal Obstruction
;
Intestinal Pseudo-Obstruction*
;
Parenteral Nutrition
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Parturition
;
Peristalsis
;
Sepsis
;
Urinary Bladder
3.An Electron Microscopic Study on Remodelling of Donor Site of Patellar Tendon Used for ACL Reconstruction.
Eun Kyoo SONG ; Keun Bae LEE ; Hyoung Yeon SEO
Journal of the Korean Knee Society 1997;9(1):1-6
An electron microscopic study was conducted in order to investigate the healing and maturation process of central one third of donor site patellar tendon which was used for endoscopic anterior cruciate ligament reconstruction. 17 patients among 118 consecutive series, which underwent ACL reconstruction from January 1990 to March 1995, were involved in this study according to various followup periods. At 6 months follow-up, hypercullular and randomly arranged fibrohlasts had abundant cytoplasm with marked irregular cytoplasmic borders and short cytoplasmic extensions. Thc, nuclei of fibroblasts had prominent nuclear indentation with chromatin condensation along the nuclear mernbrane and prominent nucleolus. The cytoplasm contained irregularly dilated rough endoplasmic reticulum, Golgi complex, and pinocytic vesicles. Intercellular space were occupied by newly-formed, immature col)agen fibrills without distinct parallel arrangement, and the diameter of collagen fibrils was unifoimly small. At 12 months, fibroblast and collagen fibrils showed a little matured findings except the small diameter of collagen fibrils. At 24 months, irregular-shaped fibroblasts were still present, which contained folded nuclei, ahundant cytoplasm with large amount of rough endoplasmic reticulum and Golgi complex. Collagen fihril showed also a unimodal distribution pattern with small diameter, however had a tendency to have a regular parallel arrangement. These finding suggest that the donor site of a patellar tendon was still quite different from normal patellar tendon in electron microscopic morphology even at 24 months postoperative follow-up regardless of considerable maturation of regular parallel arrangement pattern of collagen fibril.
Anterior Cruciate Ligament Reconstruction
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Chromatin
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Collagen
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Cytoplasm
;
Dronabinol
;
Endoplasmic Reticulum, Rough
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Extracellular Space
;
Fibroblasts
;
Follow-Up Studies
;
Golgi Apparatus
;
Humans
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Patellar Ligament*
;
Tissue Donors*
4.Nocturia.
Journal of the Korean Medical Association 2015;58(10):892-896
Nocturia is currently defined as the complaint that an individual has to wake at night > or =1 times to void. Nocturia is a highly prevalent and bothersome condition, associated with serious medical conditions, as well as increased mortality risk. However, it remains an underreported, underdiagnosed, and undertreated condition, with many patients accepting it as a natural consequence of aging. Therefore nocturia as a condition deserves public health attention. Nocturia is a multifactorial condition that can coexist with other lower urinary tract symptoms, and the most common causal factor is nighttime overproduction of urine. Recent studies have improved our understanding of nocturia while introducing a growing number of therapeutic options. This paper aims to review the classification, etiology, evaluation and treatment of nocturia to help healthcare providers better serve patients who have nocturia.
Aging
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Classification
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Fibrinogen
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Health Personnel
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Humans
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Lower Urinary Tract Symptoms
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Mortality
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Nocturia*
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Public Health
5.A Case of Combined Esophageal Atresia and Duodenal Atresia.
Ju Yeong SEO ; Cheol LEE ; Woo Yeong CHUNG ; Soon Yong LEE ; Yeon Soon KIM
Journal of the Korean Pediatric Society 1985;28(9):912-915
No abstract available.
Esophageal Atresia*
6.The clinical manifestations of the five cases of lymphangitic carci-nomatosis of the lung presented as diffuse and interstitial disease .
Young Joo SUNG ; Soo Jeon CHOI ; Bong Chun LEE ; Dong Soon KIM ; Yeon Lim SEO
Tuberculosis and Respiratory Diseases 1992;39(1):55-61
No abstract available.
Lung*
7.A Study of Genetic Inheritance of Bromidrosis.
Han Ho CHU ; Young Tae SEO ; Han Sol LEE ; Yeon Su KIM ; Yoo Hyun BANG
Journal of the Korean Society of Plastic and Reconstructive Surgeons 1999;26(2):210-214
Bromidrosis is a disorder characterized by rancid body odor which influences a patient's social life and mental health. The therapeutic modalities and the mechanism of bromidrosis have been carefully studied, however, there have been few reports about the genetic inheritance of bromidrosis. We investigated the family history of 42 patients who were operated on for bromidrosis and followed up to the third generation in 10 cases. The results were as follows: Results of investigation which were followed up the second generation. The fathers of five patients and the mothers of 11 patients had bromidrosis in 18 male patients. The fathers of six patients and the mothers of 12 patients had bromidrosis in 24 female patients. Thirty-four patient (81.0%) among a total of 42 have a single parent with bromidrosis. Result of investigation which were followed up to the third generation Bromidrosis was occurred in 17 of 42 patients (40.5%) in the second generation, and 18 of 27 patients (66.7%) in the third generation. In one case, a father transmitted bromidrosis to his three sons, and as a result, X-linked inheritance could be ruled out Bromidrosis was not skipped in every generation of all families. We on conclude that bromidrosis is an autosomal dominant inherited disorder.
Fathers
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Female
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Genes, X-Linked
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Humans
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Male
;
Mental Health
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Mothers
;
Odors
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Single Parent
;
Wills*
8.A Case of Eosinophilic Panniculitis Associated With Superior Sagittal Sinus Thrombosis.
Seung Lee SEO ; Yun Jin KIM ; Yeon Soon LIM ; Hae Young CHOI ; Ki Bum MYUNG
Annals of Dermatology 1999;11(1):37-40
Eosinophilic panniculitis is characterized by a prominent infiltration of numerous eosinophils in subcutaneous fat, and has been identified in patients with a variety of associated clinical conditions. A case of eosinophilic panniculitis in a 20-year-old woman with a history of atopic dermatitis is reported. She later developed superior sagittal sinus thrombosis, and we stress the importance of systemic evaluations in patients with eosinophilic panniculitis.
Dermatitis, Atopic
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Eosinophils*
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Female
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Humans
;
Panniculitis*
;
Subcutaneous Fat
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Superior Sagittal Sinus*
;
Thrombosis*
;
Young Adult
9.Two Cases of Rieger's Syndrome.
Journal of the Korean Ophthalmological Society 1987;28(5):1143-1153
The Rieger's syndrome is characterized by the ocular anomalies include posterior embryotoxon(a prominent Schwalbe's line), tissue strands across the anterior chamber angle and variable degrees of iridic distortion and systemic defects most often involve the teeth and facial bones. These disorders are typically bilateral, are usually diagnosed at birth or in early childhood, and most have genetic basis of autosomal dominant inheritance. A large number of patients have glaucoma due to developmental defects of the anterior chamber angle structures. The authors experienced two cases of Rieger's syndrome which were occurred in a 13-year-old female in one family and in a 21 year-old male in the other family who had characteristic ocular and other systemic abnormalities associated with developmental glaucoma.
Adolescent
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Anterior Chamber
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Facial Bones
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Female
;
Glaucoma
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Humans
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Male
;
Parturition
;
Tooth
;
Wills
;
Young Adult
10.A Case of Lacrimal Monomorphic Adenoma.
Sang Ki JEONG ; Man Seong SEO ; Yeon LEE
Journal of the Korean Ophthalmological Society 1986;27(5):925-929
The authors experienced a case of the monomorphic adenoma of lacrimal gland. Monomorphic adenoma is an extremely rare salivary gland tumor. A fifty eight year old Korean female was admitted to our Dept. of Ophthalmology because of multiple small nodular masses on her right upper eyelid and a large hard solitary mass in the supraorbital area since one year ago. On B-scan ultrasonogtaphy, round echo-free zone was detected in the superiortemporal orbit. Well defined hyperdense, enhanced round extraconal mass in the superiororbital area was detected by orbital CT scan. Two large well encapsulated, dark brown colored masses were extracted by supraorbital approach and lateral orbitotomy under general anesthesia. After removal of the masses, histopathologic examination confirmed the lacrimal monomorphic adenoma.
Adenoma*
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Anesthesia, General
;
Eyelids
;
Female
;
Humans
;
Lacrimal Apparatus
;
Ophthalmology
;
Orbit
;
Salivary Glands
;
Tomography, X-Ray Computed