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1.
The Korean Journal of Gastroenterology ; : 232-238, 2017.
Article in Korean | WPRIM | ID: wpr-51510

ABSTRACT

BACKGROUND/AIMS: The eradication rate of Helicobacter pylori (H. pylori) has been decreasing recently in Korea due to antibiotics resistance. The aim of this study was to investigate the trend of eradication rate and clinical factors affecting the eradication rate of H. pylori in the last 10 years in west Gyeonggi-do, Korea. METHODS: The trends of eradication rate of H. pylori, gender, age, concomitant mediations, and clinical factors were retrospectively evaluated in patients with H. pylori infection between 2006 and 2015 (n=2,485). RESULTS: The overall H. pylori eradication rate for the standard triple therapy was 82.5%. The annual eradication rates from 2006 to 2015 were 90%, 77.9%, 75.8%, 83.2%, 85.6%, 90.1%, 81.3%, 81.1%, 78.7%, and 78.8%, respectively, showing a significant decrement during the last five years (p < 0.001). Higher eradication rate was observed in males than in females (p < 0.001). Esomeprazole showed a higher eradication rate compared with pantoprazole between 2006 and 2010 (p < 0.022). Age and the use of probiotics and mucosal protective agents played no significant role in the H. pylori eradication rate. The overall eradication rate for bismuth-based quadruple therapy was 94.4%. CONCLUSIONS: The eradication rate of H. pylori over the last 10 years for first-line therapy ranged from 75.8 to 90.1%; the eradication rate for triple therapy has declined. However, the eradication rate for quadruple therapy has remained unchanged over the last 10 years.


Subject(s)
Female , Humans , Male , Anti-Bacterial Agents , Disease Eradication , Esomeprazole , Helicobacter pylori , Helicobacter , Korea , Probiotics , Protective Agents , Retrospective Studies
2.
The Korean Journal of Helicobacter and Upper Gastrointestinal Research ; : 165-168, 2016.
Article in Korean | WPRIM | ID: wpr-222505

ABSTRACT

Upper gastrointestinal bleeding is a common condition and has various clinical courses and prognosis. End stage renal disease (ESRD) patients receiving hemodialysis have a high risk of vascular complications and increased risk of ischemic colitis. A 59-year-old male patient with ESRD receiving hemodialysis visited due to hematemesis. After admission, he showed recurrent hematemesis and hypovolemic shock. Upper esophagogastroduodenoscopy revealed gastric ulcer bleeding and endoscopic hemostasis was successfully performed. Blood transfusion and norepinephrine was administered for hypovolemic shock during initial 3 days. Ten days later, he exhibited hematochezia. Sigmoidoscopy revealed necrotic ischemic colitis in sigmoid colon and segmental colectomy was performed. However, recurrent leakage and ischemia were developed in colon as well as small bowel, and he finally died after 55 hospital days in spite of additional operations. Here, we report a case of peptic ulcer bleeding in patient with ESRD who suffered a severe form of ischemic colitis with transmural necrosis.


Subject(s)
Humans , Male , Middle Aged , Blood Transfusion , Colectomy , Colitis, Ischemic , Colon , Colon, Sigmoid , Endoscopy, Digestive System , Gastrointestinal Hemorrhage , Hematemesis , Hemorrhage , Hemostasis, Endoscopic , Ischemia , Kidney Failure, Chronic , Necrosis , Norepinephrine , Peptic Ulcer , Prognosis , Renal Dialysis , Shock , Sigmoidoscopy , Stomach Ulcer
3.
The Korean Journal of Helicobacter and Upper Gastrointestinal Research ; : 178-181, 2015.
Article in English | WPRIM | ID: wpr-179128

ABSTRACT

Mesenteric panniculitis (MP) is non-specific inflammation of the adipose tissue that primarily involves the small bowel mesentery. Omental involvement has been rarely reported but we report a case of 25 years old woman with isolated lesser omental panniculitis. This patient was diagnosed by CT findings and recovered completely with conservative treatment. Invasive diagnostic methods or surgical exploration has been used to diagnose MP. However, all six reported cases of omental panniculitis including the current case showed a benign course; therefore, awareness of the CT findings is essential for the best diagnosis and management of omental panniculitis.


Subject(s)
Female , Humans , Adipose Tissue , Anti-Inflammatory Agents, Non-Steroidal , Diagnosis , Inflammation , Mesentery , Omentum , Panniculitis , Panniculitis, Peritoneal , Tomography, X-Ray Computed
4.
Journal of the Korean Association of Maxillofacial Plastic and Reconstructive Surgeons ; : 41-45, 2009.
Article in Korean | WPRIM | ID: wpr-784872
5.
Journal of the Korean Association of Maxillofacial Plastic and Reconstructive Surgeons ; : 407-416, 2008.
Article in Korean | WPRIM | ID: wpr-784848
6.
Journal of the Korean Association of Maxillofacial Plastic and Reconstructive Surgeons ; : 495-499, 2008.
Article in Korean | WPRIM | ID: wpr-784838
7.
Journal of the Korean Association of Maxillofacial Plastic and Reconstructive Surgeons ; : 302-309, 2008.
Article in Korean | WPRIM | ID: wpr-784815
8.
Journal of the Korean Association of Maxillofacial Plastic and Reconstructive Surgeons ; : 114-116, 2008.
Article in Korean | WPRIM | ID: wpr-784790
9.
Journal of the Korean Association of Oral and Maxillofacial Surgeons ; : 509-517, 2008.
Article in Korean | WPRIM | ID: wpr-75368

ABSTRACT

DNA damage accumulates in cells as a result of exposure to exogenous agents such as benzopyrene, cigarette smoke, ultraviolet light, X-ray, and endogenous chemicals including reactive oxygen species produced from normal metabolic byproducts. DNA damage can also occur during aberrant DNA processing reactions such as DNA replication, recombination, and repair. The major of DNA damage affects the primary structure of the double helix; that is, the bases are chemically modified. These modification can disrupt the molecules' regular helical structure by introducing non-native chemical bonds or bulky adducts that do not fit in the standard double helix. DNA repair genes and proteins scan the global genome to detect and remove DNA damage and damage to single nucleotides. Direct reversal of DNA damage, base excision repair, double strand break. DNA repair are known relevant DNA repair mechanisms. Four different mechanisms are distinguished within excision repair: direct reversal, base excision repair, nucleotide excision repair, and mismatch repair. Genetic variation in DNA repair genes can modulate DNA repair capacity and alter cancer risk. The instability of a cell to properly regulate its proliferation in the presence of DNA damage increase risk of gene mutation and carcinogenesis. This article aimed to review mechanism of excision repair and to understand the relationship between genetic variation of excision repair genes and head and neck cancer.


Subject(s)
DNA , DNA Damage , DNA Mismatch Repair , DNA Repair , DNA Replication , Genetic Variation , Genome , Head , Head and Neck Neoplasms , Nucleotides , Proteins , Reactive Oxygen Species , Recombination, Genetic , Smoke , Tobacco Products , Ultraviolet Rays
10.
Journal of the Korean Association of Oral and Maxillofacial Surgeons ; : 450-455, 2008.
Article in Korean | WPRIM | ID: wpr-205954

ABSTRACT

A Single Nucleotide Polymorphism (SNP) is a small genetic change or variation that can occur within a DNA sequence. It's the difference of one base at specific base pair position. SNP variation occurs when a single nucleotide, such as an A, replaces one of the other three nucleotide letters-C, G, or T. On average, SNP occur in the human population more than 1 percent of the time. They occur once in every 300 nucleotides on average, which means there are roughly 10 million SNPs in the human genome. Because SNPs occur frequently throughout the genome and tend to be relatively stable genetically, they serve as excellent biological markers. They can help scientists locate genes that are associated with disease such as heart disease, cancer, diabetes. They can also be used to track the inheritance of disease genes within families. SNPs may also be associated with absorbance and clearance of therapeutic agents. In the future, the most appropriate drug for an individual could be determined in advance of treatment by analyzing a patient's SNP profile. This pharmacogenetic strategy heralds an era in which the choice of drugs for a particular patient will be based on evidence rather than trial and error (so called" personalized medicine").


Subject(s)
Humans , Base Pairing , Base Sequence , Biomarkers , Genome , Genome, Human , Heart Diseases , Precision Medicine , Nucleotides , Polymorphism, Single Nucleotide , Track and Field , Wills
11.
Journal of the Korean Association of Maxillofacial Plastic and Reconstructive Surgeons ; : 456-462, 2007.
Article in Korean | WPRIM | ID: wpr-784768
14.
Journal of the Korean Association of Oral and Maxillofacial Surgeons ; : 481-491, 2005.
Article in Korean | WPRIM | ID: wpr-69183

ABSTRACT

PURPOSE: The aim of the present study is to evaluate the effect of autogenous bone and allograft material coverd with a bioresorbable membrane on bone regeneration after a simultaneous installation of implant. MATERIALS AND METHODS: Twelve healthy rabbits, weighing about 3~4 kg, were used in this experiment. Following impalnt(with 3.25 mm diameter and 8 mm length) site preparation by surgical protocol of Oraltronics(R), artificial bony defect, 5mm sized in height and depth, was created on femoral condyle using trephine drill(with 5 mm diameter and 5 mm length). Then implant was inserted. In the experimental group A, the bony defect was filled with autogenous particulated bone and coverd with Lyoplant(R) resorbable membrane. In the experimental group B, the bony defect was filled with allograft material(Orthoblast II(R)) containing demineralized bone matrix and covered with Lyoplant(R). In the control group, without any graft materials, the bony defect was covered with Lyoplant(R). The experimental group A and B were divided into each 9 cases and control group into 3 cases. The experimental animals were sacrificed at 3, 6 and 8 weeks after surgery and block specimens were obtained. With histologic and histomorphometric analysis, we observed the histologic changes of the cells and bone formation after H-E staining and then, measured BIC and bone density with KAPPA Image Base(R) system. RESULTS: As a result of this experiment, bone formation and active remodeling process were examined in all experimental groups and the control. But, the ability of bone formation of the experimental group A was somewhat better than any other groups. Especially bone to-implant contact fraction ranged from 12.7% to 43.45% in the autogenous bone group and from 9.02% to 29.83% in DBM group, at 3 and 8 weeks. But, bone density ranged from 15.67% to 23.17% in the autogenous bone group and from 25.95% to 46.06% in DBM group at 3 and 6 weeks, respectively. Although the bone density of DBM group was better than that of autogenous bone group at 3 and 6weeks, the latter was better than the former at 8 weeks, 54.3% and 45.1%, respectively. Therefore these results showed that DBM enhanced the density of newly formed bone at least initially.


Subject(s)
Animals , Rabbits , Allografts , Bone Density , Bone Matrix , Bone Regeneration , Membranes , Osteogenesis , Transplants
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