1.Role of immunotherapy combined with chemotherapy in newly diagnosed pulmonary tuberculosis patients
Journal of Preventive Medicine 1998;8(1):28-34
The preliminary results showed that the immunotherapy with M.Vaccae may be very effective. 13 of 20 patients without immunotherapy (group A) have improved clinically, comparing with 22 improved patients of 22 patients with immunotherapy (group B), especially, 4 of 20 patients in group A had a relapse after treatment, and the difference of immune responses between 2 groups in the end of treatment could be found out.
Tuberculosis, Pulmonary
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Immunotherapy
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Drug Therapy
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Diagnosis
2.Clinical Pharmacogenetic Testing and Application: Laboratory Medicine Clinical Practice Guidelines.
Sollip KIM ; Yeo Min YUN ; Hyo Jin CHAE ; Hyun Jung CHO ; Misuk JI ; In Suk KIM ; Kyung A WEE ; Woochang LEE ; Sang Hoon SONG ; Hye In WOO ; Soo Youn LEE ; Sail CHUN
Annals of Laboratory Medicine 2017;37(2):180-193
Pharmacogenetic testing for clinical applications is steadily increasing. Correct and adequate use of pharmacogenetic tests is important to reduce unnecessary medical costs and adverse patient outcomes. This document contains recommended pharmacogenetic testing guidelines for clinical application, interpretation, and result reporting through a literature review and evidence-based expert opinions for the clinical pharmacogenetic testing covered by public medical insurance in Korea. This document aims to improve the utility of pharmacogenetic testing in routine clinical settings.
Anticoagulants/therapeutic use
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Antidepressive Agents/therapeutic use
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Antimetabolites, Antineoplastic/therapeutic use
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Antitubercular Agents/therapeutic use
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Arylamine N-Acetyltransferase/genetics
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Coronary Artery Disease/drug therapy/genetics
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Cytochrome P-450 CYP2C19/genetics
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Cytochrome P-450 CYP2C9/genetics
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Cytochrome P-450 CYP2D6/genetics
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Depressive Disorder/drug therapy/genetics
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Genotype
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Isoniazid/therapeutic use
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Laboratories, Hospital/standards
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Methyltransferases/genetics
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Pharmacogenomic Testing/*methods/standards
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Platelet Aggregation Inhibitors/therapeutic use
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Pulmonary Embolism/drug therapy/genetics
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Ticlopidine/analogs & derivatives/therapeutic use
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Tuberculosis/drug therapy/genetics
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Vitamin K Epoxide Reductases/genetics
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Warfarin/therapeutic use
3.Severe Pulmonary Adverse Effects in Lymphoma Patients Treated with Cyclophosphamide, Doxorubicin, Vincristine, and Prednisone (CHOP) Regimen Plus Rituximab.
Kyu Hyoung LIM ; Ho Il YOON ; Young Ae KANG ; Keun Wook LEE ; Jee Hyun KIM ; Soo Mee BANG ; Jae Ho LEE ; Choon Taek LEE ; Jong Seok LEE
The Korean Journal of Internal Medicine 2010;25(1):86-92
BACKGROUND/AIMS: The aim of our study was to determine the incidence and clinical features of severe pulmonary complications in patients receiving cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) or rituximab plus CHOP (R-CHOP) as the initial treatment for lymphoma. METHODS: A retrospective analysis of pulmonary infection and drug-induced interstitial pneumonitis (DIIP) was performed using lymphoma registry data. R-CHOP was administered in 71 patients and CHOP in 29 patients. RESULTS: The severe pulmonary adverse events tended to occur more frequently with R-CHOP (18.3%) than CHOP alone (13.8%), although the difference was not significant (p = 0.771). DIIP occurred in five patients in the R-CHOP arm (7%) and in one in the CHOP arm (3%). The continuous use of steroids for conditions other than lymphoma significantly increased the risk of pulmonary infection including Pneumocystis jiroveci pneumonia (p = 0.036) in the multivariate analysis. International prognostic index, tumor stage, smoking, previous tuberculosis, chronic obstructive pulmonary disease, and lymphoma involvement of lung parenchyma were not related to pulmonary adverse events. Patients who experienced severe pulmonary events showed shorter survival when compared to those without complications (p = 0.002). CONCLUSIONS: Our experiences with serial cases with DIIP during chemotherapy and the correlation of continuous steroid use with pulmonary infection suggest that the incidence of pulmonary complications might be high during lymphoma treatment, and careful monitoring should be performed.
Adult
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Aged
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Aged, 80 and over
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Antibodies, Monoclonal/administration & dosage/*adverse effects
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Antineoplastic Combined Chemotherapy Protocols/administration & dosage/*adverse effects
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Cyclophosphamide/administration & dosage/adverse effects
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Doxorubicin/administration & dosage/adverse effects
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Female
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Humans
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Incidence
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Lung Diseases, Interstitial/*chemically induced/mortality
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Lymphoma, Non-Hodgkin/*drug therapy/mortality
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Male
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Middle Aged
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Pneumocystis jirovecii
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Pneumonia, Bacterial/mortality
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Pneumonia, Pneumocystis/mortality
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Prednisone/administration & dosage/adverse effects
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Retrospective Studies
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Risk Factors
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Severity of Illness Index
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Tuberculosis, Pulmonary/mortality
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Vincristine/administration & dosage/adverse effects
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Young Adult