1.Temporal Trends of Cardiac Implantable Electronic Device Implantations: a Nationwide Population-based Study
Ji Hyun LEE ; So Ryoung LEE ; Eue Keun CHOI ; Jaehan JEONG ; Hyung Deuk PARK ; So Jeong YOU ; Sang Soo LEE ; Seil OH
Korean Circulation Journal 2019;49(9):841-852
BACKGROUND AND OBJECTIVES: Implantation of cardiac implantable electronic devices (CIED), including permanent pacemakers (PM), implantable cardioverter-defibrillators (ICD), and cardiac resynchronization therapy (CRT) devices, has increased significantly over the past several years. However, limited data exists regarding temporal trends of CIED implantations in Asian population. This study aimed to investigate temporal trends of CIED treatment in Korea. METHODS: Using the National Health Insurance Service database of the entire Korean adult population, temporal trends of CIED procedures between 2009 and 2016 were evaluated. Additionally, temporal changes in the prevalence of patients' comorbidities were evaluated. RESULTS: A total of 35,421 CIED procedures (new implantations: 27,771, replacements: 7,650) were performed during the study period. The mean age of new CIED recipients and the prevalence of comorbidities, including hypertension, diabetes mellitus, heart failure, stroke, and atrial fibrillation, increased substantially with time. Compared to 2009, the number of new implantations of PM, ICD, and CRT devices increased by 2.0 (1,977 to 3,910), 3.6 (230 to 822), and 4.9 (44 to 217) times in 2016, respectively. The annual new implantation rate of CIED also increased accordingly (5.1 to 9.3 for PM, 0.6 to 1.9 for ICD, and 0.1 to 0.5 for CRT devices, per 100,000 persons). CONCLUSIONS: The number of CIED implantation increased substantially from 2009 to 2016 in Korea. Also, the patients with CIED have been changed to be older and have more comorbidities. Therefore, the burden of health care cost in patients with CIED would be expected to increase in the future.
Adult
;
Asian Continental Ancestry Group
;
Atrial Fibrillation
;
Cardiac Resynchronization Therapy
;
Comorbidity
;
Defibrillators, Implantable
;
Diabetes Mellitus
;
Epidemiology
;
Health Care Costs
;
Heart Failure
;
Humans
;
Hypertension
;
Korea
;
National Health Programs
;
Pacemaker, Artificial
;
Prevalence
;
Stroke
2.Temporal Trends of Cardiac Implantable Electronic Device Implantations: a Nationwide Population-based Study
Ji Hyun LEE ; So Ryoung LEE ; Eue Keun CHOI ; Jaehan JEONG ; Hyung Deuk PARK ; So Jeong YOU ; Sang Soo LEE ; Seil OH
Korean Circulation Journal 2019;49(9):841-852
BACKGROUND AND OBJECTIVES:
Implantation of cardiac implantable electronic devices (CIED), including permanent pacemakers (PM), implantable cardioverter-defibrillators (ICD), and cardiac resynchronization therapy (CRT) devices, has increased significantly over the past several years. However, limited data exists regarding temporal trends of CIED implantations in Asian population. This study aimed to investigate temporal trends of CIED treatment in Korea.
METHODS:
Using the National Health Insurance Service database of the entire Korean adult population, temporal trends of CIED procedures between 2009 and 2016 were evaluated. Additionally, temporal changes in the prevalence of patients' comorbidities were evaluated.
RESULTS:
A total of 35,421 CIED procedures (new implantations: 27,771, replacements: 7,650) were performed during the study period. The mean age of new CIED recipients and the prevalence of comorbidities, including hypertension, diabetes mellitus, heart failure, stroke, and atrial fibrillation, increased substantially with time. Compared to 2009, the number of new implantations of PM, ICD, and CRT devices increased by 2.0 (1,977 to 3,910), 3.6 (230 to 822), and 4.9 (44 to 217) times in 2016, respectively. The annual new implantation rate of CIED also increased accordingly (5.1 to 9.3 for PM, 0.6 to 1.9 for ICD, and 0.1 to 0.5 for CRT devices, per 100,000 persons).
CONCLUSIONS
The number of CIED implantation increased substantially from 2009 to 2016 in Korea. Also, the patients with CIED have been changed to be older and have more comorbidities. Therefore, the burden of health care cost in patients with CIED would be expected to increase in the future.
3.A Case of Multiple Miliary Osteomas of the Face.
So Youn KIM ; Young Eun CHO ; You Won CHOI ; Kyu Kwang WHANG ; Jeong Hee HAHM
Korean Journal of Dermatology 2003;41(10):1378-1380
Osteoma cutis is a rare disorder characterized by compact bone formation in the dermis and subcutaneous tissue. It is classified in primary and secondary forms according to the presence or absence of previous cutaneous lesions. Multiple miliary osteomas of the face is a form of primary miliary osteoma cutis that generally occurs in middle-aged and older women. We report a typical case of multiple miliary osteomas of the face in a 63-year-old woman.
Dermis
;
Female
;
Humans
;
Middle Aged
;
Osteogenesis
;
Osteoma*
;
Subcutaneous Tissue
4.A Case of Hemifacial Hypertrophy due to Plexiform Neurofibroma with the Cafe-au-lait Macules.
Jeong Eun DO ; Hee Young KANG ; Eun So LEE ; You Chan KIM
Korean Journal of Dermatology 2009;47(1):89-94
Plexiform neurofibromas are among the most pathognomonic features of neurofibromatosis type 1 (NF1). Although characteristically benign, plexiform neurofibroma can cause pain, disfigurement and functional changes, and more importantly, it may turn malignant. We present here the case of a 3-year-old boy with progressive hemifacial hypertrophy that was colocalized with light brown-colored macules. The biopsy specimen showed that the bundles of nerve fibers were arranged in a concentric manner with myxoid changes. On the evaluation of the pigmented lesion, only the basal melanin pigments were increased in the epidermis without any melanin-laden pigmented cells in the dermis. We have demonstrated that neurofbroma needs to be considered in the differential diagnosis of hemifacial hypertrophy since this is likely to have implications for the further management of these patients. The absence of other findings does not exclude NF1 as the underlying disease since many NF1 patients have not yet developed cafe-au-lait macules or freckles in early childhood.
Biopsy
;
Dermis
;
Diagnosis, Differential
;
Epidermis
;
Humans
;
Hypertrophy
;
Light
;
Melanins
;
Melanosis
;
Nerve Fibers
;
Neurofibroma, Plexiform
;
Neurofibromatosis 1
;
Preschool Child
5.A Case of Primary Cutaneous Anaplastic Large Cell Lymphoma with Extensive Inflammatory Cell Infiltration.
Jeong Eun DO ; En Hyung KIM ; Hee Young KANG ; Eun So LEE ; You Chan KIM
Korean Journal of Dermatology 2008;46(2):268-271
Primary cutaneous anaplastic large cell lymphoma (ALCL) is composed of large cells with anaplastic, pleomorphic cytomorphology and the expression of the CD30 antigen by the majority (more than 75%) of tumor cells. Recently some variants of ALCL with extensive inflammatory cell infiltration have been reported. A 34-year-old male presented with multiple tumors over the arm, groin, and legs. The tumors of the right groin showed ulceration and purulent discharge. The biopsy specimens revealed extensive infiltrate of large atypical lymphoid cells with mixed inflammatory cells consisting of numerous eosinophils and neutrophils. Immunohistochemical staining was positive for CD3, CD4, and CD30. TCR-gamma gene rearrangement was detected. There was no evidence of extracutaneous involvement. We report a case of primary cutaneous ALCL, associated with marked inflammatory cell infiltration. Diagnosis in such cases is challenging because the large atypical lymphoid cells may be easily obscured by the massive infiltrate of eosinophils and neutrophils.
Adult
;
Antigens, CD30
;
Arm
;
Biopsy
;
Eosinophils
;
Gene Rearrangement
;
Groin
;
Humans
;
Leg
;
Lymphocytes
;
Lymphoma, Primary Cutaneous Anaplastic Large Cell
;
Male
;
Neutrophils
;
Ulcer
6.Plasma G-CSF and GM-CSF Concentrations and Expression of their Receptors on the Granulocyte in Children with Leukocytosis.
Won Seok CHOI ; Kyung Hwan RYU ; You Jeong KIM ; So Young KIM ; Hyun Hee KIM ; Wonbae LEE
Journal of the Korean Pediatric Society 2003;46(3):271-276
PURPOSE: Granulocyte-colony stimulating factor(G-CSF) and granulocyte macrophage-colony stimulating factor(GM-CSF) are principal cytokines in granulopoiesis and their physiologic effects are mediated through binding to specific cell surface receptors. Although it is known that the level of serum G-CSF and GM-CSF, and presentation of the receptors are increased in infectious diseases, there have been no studies to find the correlation between the granulopoiesis and leukocytosis. This study was designed to measure G-CSF and GM-CSF in leukocytosis and in control and to demonstrate the possible pathogenesis of granulopoiesis in leukocytosis using quantitative analysis of G- CSF, GM-CSF and their CSFr. METHODS: The plasma levels of G-CSF, GM-CSF of 13 children without leukocytosis and 14 children with leukocytosis were measured. Counts of cell surface G-CSFr and GM-CSFr were measured by combining anti G-CSFr and anti GM-CSFr monoclonal antibodies to their respective receptors by using quantitative flow cytometric assay. RESULTS: There was no significant difference betweeen the plasma concentration of G-CSF and GM-CSF in acute leukocytosis and in the control group. However, levels of G-CSFr in acute leukocytosis decreased significantly compared to the control(P=0.012) and the levels of GM-CSFr in both groups revealed no significant difference. CONCLUSION: Increase in the number of leukocyte in leukocytosis was mediated by increasing the number of neutrophil, and increased plasma concentration of G-CSF may be the cause of neutrophilia. But GM-CSF did not have any influence on leukocytosis.
Antibodies, Monoclonal
;
Child*
;
Communicable Diseases
;
Cytokines
;
Granulocyte Colony-Stimulating Factor*
;
Granulocyte-Macrophage Colony-Stimulating Factor*
;
Granulocytes*
;
Humans
;
Leukocytes
;
Leukocytosis*
;
Neutrophils
;
Plasma*
;
Receptors, Cell Surface
;
Receptors, Granulocyte Colony-Stimulating Factor
;
Receptors, Granulocyte-Macrophage Colony-Stimulating Factor
7.Surgical Correction Of Congenital Earlobe Cleft Using Reverse L-Plasty.
You Jin LEE ; So Min KANG ; Jeong Yeol YANG ; Ji Sun CHEON
Journal of the Korean Cleft Palate-Craniofacial Association 2003;4(2):160-164
Congenital earlobe deformity and the presence of the cleft at a site of the earlobe seems to be rare. It is important to well-formed, symmetrically positioned ears as a sign of esthetically pleasing, harmonious facial features. So the patients with cleft earlobe require operative repairs. The surgical techniques for congenital earlobe clefts employed vary from simple closure, Z-plasty, L-plasty, two flap method, triangular flap method, and so on. Among them, Passow-Claus described the classic L-plasty method. We designed the modified method that the L-flap direction faced laterally opposed to that of classic L-plasty and propose to term this method `reverse L-plasty`. Kitayama classified the congenital earlobe cleft into four groups according to the shape of cleft, as longitudinal, transverse, triplelobe or mixed, and defective type. We experienced four cases of congenital earlobe cleft. One patient was a defective type and the others were triplelobe types. There`s no complication in patients. We could obtain the advantages of smooth contour of free border, lack of groove or notching due to scar contracture, and possible in moderate defective type without additional method after long term follow-up. This technique breaks the vertical component of scar contracture, resulting in a smooth lobular border. So we believe that this reverse L-plasty technique offers a better cosmetic result in the repair of the cleft earlobe.
Cicatrix
;
Congenital Abnormalities
;
Contracture
;
Ear
;
Follow-Up Studies
;
Humans
8.A Case of Bilateral Congenital Nasolacrimal Duct Cysts Presenting as Neonatal Respiratory Distress.
Dae Hyoung LEE ; Hye Rin MOK ; Hyun Hee KIM ; So Young KIM ; You Jeong KIM ; Wonbae LEE
Korean Journal of Perinatology 2003;14(3):316-319
Congenital nasolacrimal duct cyst is an uncommon anomaly of nasolacrimal duct obstruction in the newborn. It is cystic dilation of the lower end of the unperforated nasolacrimal duct with intranasal extension. In such cases, the bluish-gray cyst arises beneath the inferior turbinate on nasal endoscopy. A large nasolacrimal duct cyst can fill the nasal cavity and lead to nasal obstruction. Neonates are obligate nasal breathers at birth and require several weeks to learn to breathe through the mouth. Consequently this nasal obstruction can cause significant respiratory distress. We experienced a case of bilateral nasolacrimal duct cyst presenting as neonatal respiratory distress. Diagnosis was confirmed by nasal endoscopy and CT scan. After endoscopic marsupialization of the cysts , symptom and sign of respiratory distress were rapidly resolved.
Diagnosis
;
Endoscopy
;
Humans
;
Infant, Newborn
;
Mouth
;
Nasal Cavity
;
Nasal Obstruction
;
Nasolacrimal Duct*
;
Parturition
;
Tomography, X-Ray Computed
;
Turbinates
9.A Case of Localized Erythematous Dermatitis on the Site of a Docetaxel Injection.
Jeong Eun DO ; You Chan KIM ; Eun So LEE ; Hee Young KANG
Korean Journal of Dermatology 2007;45(7):739-741
Docetaxel is a taxoid antineoplastic drug widely used for various advanced solid tumors. Docetaxel-induced cutaneous adverse reactions include acral erythema, pigmentaion disorders and nail changes. Herein we report a case of recurrent erythematous dermatitis which was localized on the site of a docetaxel injection in a 48-year-old patient with advanced gastric cancer. Histopathological findings were consistent with erythema multiforme.
Dermatitis*
;
Erythema
;
Erythema Multiforme
;
Humans
;
Middle Aged
;
Stomach Neoplasms
10.A Case of Frontal Fibrosing Alopecia.
So Youn KIM ; You Won CHOI ; Kyu Kwang WHANG ; Jeong Hee HAHM
Korean Journal of Dermatology 2005;43(7):976-978
Frontal fibrosing alopecia is considered to be a clinical variant of lichen planopilaris. This condition is characterized by progressive frontal hairline recession associated with scarring. Frontal fibrosing alopecia has become an increasingly recognized distinct clinical entity in recent years. We report a typical case of frontal fibrosing alopecia and review the pertinent literature.
Alopecia*
;
Cicatrix
;
Lichens