2.Never Get Ahead of Others.
Clinics in Orthopedic Surgery 2010;2(2):63-63
No abstract available.
Diffusion of Innovation
;
Humans
;
Learning Curve
;
*Orthopedic Procedures/adverse effects
3.Intravesical Therapy for Superficial Bladder Cancer: Advances and Future.
Korean Journal of Urology 2000;41(4):467-479
No abstract available.
Urinary Bladder Neoplasms*
;
Urinary Bladder*
4.Linkage between gene marker of chromosome 11q13 and IgE-receptor mediated basophil histamine release.
Korean Journal of Medicine 1999;56(5):665-665
No abstract available.
Basophils*
;
Histamine Release*
;
Histamine*
5.Novel oral anticoagulants for atrial fibrillation.
Singapore medical journal 2015;56(12):657-quiz 659
Anticoagulation therapy is effective in preventing primary and secondary thromboembolic events due to atrial fibrillation. Warfarin, which was approved by the United States in 1954, was the only long-term oral anticoagulation therapy till the approval of dabigatran in 2010, and of rivaroxaban and other direct factor Xa inhibitors from 2011, forming a group known as novel oral anticoagulants (NOAC). NOAC have fewer food and drug interactions compared to warfarin; hence, the patient will require fewer clinic visits. However, the short half-life of NOAC means that twice-a-day dosing is needed and there is higher risk of a prothrombotic state when doses are missed. Other disadvantages are the lack of long-term data on NOAC, their high cost and the current lack of locally available antidotes.
Administration, Oral
;
Anticoagulants
;
administration & dosage
;
Atrial Fibrillation
;
drug therapy
;
Cardiology
;
methods
;
Dabigatran
;
administration & dosage
;
Family
;
Humans
;
Professional-Patient Relations
;
Rivaroxaban
;
administration & dosage
;
Stroke
;
prevention & control
;
Thromboembolism
;
prevention & control
;
Warfarin
;
administration & dosage
7.Hepatorenal Syndrome.
The Korean Journal of Hepatology 1997;3(2):89-107
No abstract available.
Hepatorenal Syndrome*
8.Management of Low Back Pain in Outpatient Clinic.
Journal of the Korean Medical Association 2000;43(9):821-830
No abstract available.
Ambulatory Care Facilities*
;
Humans
;
Low Back Pain*
;
Outpatients*
9.The effect of Oral Cryotherapy in Prevention of Oral Mucositis for Anti-Cancer Chemotherapy Patients.
Journal of Korean Academy of Adult Nursing 1997;9(2):313-323
The purpose of this study is to determine the effect of oral cryotherapy on oral mucositis in the patients who receiving high-dose ARA-C plus Mitoxantrone chemotherapy regimen. There were total of ten patients who received the chemotherapy regimen for 13 months ; 5 patients for the experimental group, while the others for the control group. The tool used for assess degree of oral mucositis was the Oral Assessment Guide(OAG) which was developed by Elier, Burger, Peterson in 1988. []The experimental group received oral cryotherapy range from 30minutes before the Mitroxantrone IV infusing to 30minutes after the high-dose ARA-C IV infusing. The control group was not treated by oral cryotherapy. The effect of this treatment was analyzed with the OAG score. The collected data were analysed with, mean, Mann-Whitney U test and Chi-square test according to characteristics of variables. The results were as follows : 1. There were no statistical difference in general characteristics(age, sex, cycle of the chemotherapy, smoking, alcohol) between the two groups, so the homogeneity of two groups was established. There were no differences in the OAG Scores between the two groups statistically. 2. The subjects of this study suffered the neutropenia from 5.6 days to 24.6 days after starting chemotherapy. During the neutropenia period the average OAG scores in the experimental group were lower than that of the control group(experimental group was 9.17+/-1.91, control group was 9.33+/-1.10). 3. The mean OAG of experimental group for 21 days was 204.72+/-20.61, while the mean of control group for 21 days was 206.23+/-15.97. There were, however, no differences between the experimental and the control groups statistically. The subjects of the experimental group expressed more comfortable oral condition than those of the past cycle and they would like to try oral cryotherapy again for the next chemotherapy. The subjects of this study suffered the neutropenia from 5.6 days to 24.6 days after starting chemotherapy. During the neutropenia period the average OAG scores in the experimental group were lower than that of the control group(experimental group was 9.17, control group was 9.33). 5 subjects of the study group complained of numbness, 3 subjects complained of slight headache, and 2 subjects expressed teeth and abdominal discomfort. However, these signs occurred temporarily and were resolved rapidly after cessation of the cryotherapy. It was I recommended that replication with larger sample.
Cryotherapy*
;
Cytarabine
;
Drug Therapy*
;
Headache
;
Humans
;
Hypesthesia
;
Mitoxantrone
;
Neutropenia
;
Smoke
;
Smoking
;
Stomatitis*
;
Tooth
10.Enhancement of Cytotoxicity by the Combination of Anticancer Drugs in Human Lung Adenocarcinoma Cell Line (PC-14).
Tuberculosis and Respiratory Diseases 1997;44(3):525-533
BACKGROUND: No ideal combination chemotherapy for lung cancer has been established even though lots of combination anticancer chemotherapies have been tried. For the combination of anticancer drugs, the interaction of anticancer drugs is very important but unpredictable factor. In this experiments we designed and tested new experiment to measure the interaction of two anticancer drugs using MTT assay in an attempt to predict clinical response of the combination regimen. METHODS: With human lung adenocarcinoma cell line (PC-14), the cytotoxic effect of cisplatin adriamycin mitomycin C and etoposide were measured by in Vitro chemosensitivity test (MTT assay). The combined cytotexic effects of combination of two drugs were also measured in every combination of the drug concentrations and analyzed the interaction by Anova analysis of two way factorial design. RESULTS: Four individual drugs showed cytotoxic effects on PC-14 by dose dependent fashion Comparison of two drug combinations revealed that mitomycin C + cisplatin and adriamycin + cisplatin combinations showed stronger synergistic cytotoxic effects. CONCLUSION: From this experiments we suggest two combinations of mitomycin C + cisplatin and adriamycin + cisplatin as chemotherapeutic regimens for unresectable non-small cell lung cancer. Furthermore, this experimental deign could be applied b other types of cancer requiring combination anticancer chemotherapy.
Adenocarcinoma*
;
Carcinoma, Non-Small-Cell Lung
;
Cell Line*
;
Cisplatin
;
Doxorubicin
;
Drug Combinations
;
Drug Therapy
;
Drug Therapy, Combination
;
Etoposide
;
Humans*
;
Lung Neoplasms
;
Lung*
;
Mitomycin