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Therapeutic Methods and Therapies TCIM
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1.
Int J Tuberc Lung Dis ; 16(12): 1605-12, 2012 Dec.
Article in English | MEDLINE | ID: mdl-23131257

ABSTRACT

SETTING: A total of 663 human immunodeficiency virus (HIV) care and treatment sites in nine tuberculosis (TB) affected African countries, serving over 900,000 persons living with HIV. OBJECTIVE: To determine the implementation of infection control (IC) measures and whether program and facility characteristics were associated with implementation of these measures. DESIGN: A survey was conducted to assess the presence of a TB IC plan, triage practices for TB suspects, location of sputum collection and availability of particulate respirators. The association of facility characteristics with IC measures was examined using bivariate and multivariate methods. RESULTS: Forty-seven per cent (range across countries [RAC] 2-77%) of sites had written TB IC plans; 60% (RAC 5-93%) practiced triage; of those with access to microscopy, 83% (RAC 59-91%) performed sputum collection outdoors and 13% (RAC 0-36%) in ventilated indoor rooms; 16% (RAC 1-87%) had particulate respirators available. Sites providing anti-tuberculosis treatment were more likely to have written IC plans (54% vs. 12%, P < 0.0001) and particulate respirators (18% vs. 8%, P = 0.0126), and to perform TB triage (65% vs. 40%, P = 0.0001) than those without anti-tuberculosis treatment services. CONCLUSIONS: To protect HIV-infected patients and health care workers, there is an urgent need to scale up IC practices at HIV care and treatment sites, particularly at sites without anti-tuberculosis treatment services.


Subject(s)
Coinfection/prevention & control , Cross Infection/prevention & control , HIV Infections/therapy , Health Facilities , Health Personnel , Infection Control/methods , Infectious Disease Transmission, Patient-to-Professional/prevention & control , Occupational Health , Tuberculosis, Pulmonary/prevention & control , Africa South of the Sahara/epidemiology , Chi-Square Distribution , Coinfection/diagnosis , Coinfection/epidemiology , Critical Pathways , Cross Infection/diagnosis , Cross Infection/epidemiology , Cross Infection/transmission , Facility Design and Construction , HIV Infections/diagnosis , HIV Infections/epidemiology , Health Care Surveys , Humans , Logistic Models , Multivariate Analysis , Mycobacterium tuberculosis/isolation & purification , Occupational Exposure , Respiratory Protective Devices , Sputum/microbiology , Triage , Tuberculosis, Pulmonary/diagnosis , Tuberculosis, Pulmonary/epidemiology , Tuberculosis, Pulmonary/transmission , Ventilation , Workforce
2.
Food Chem Toxicol ; 38(12): 1085-8, 2000 Dec.
Article in English | MEDLINE | ID: mdl-11033196

ABSTRACT

The effect of black tea polyphenols on 1,2-dimethylhydrazine (DMH)-induced oxidative DNA damage in rat colon mucosa has been investigated. Fischer 344 rats were treated orally with thearubigin (TR) or theafulvin (TFu) for 10 days (40 mg/kg), injected ip with DMH (20 mg/kg) or saline and sacrificed 24 hr after DMH administration. The levels of 8-hydroxy-2'-deoxyguanosine (8-OHdG) were measured in colonic mucosa DNA and expressed as a ratio relative to 2'-deoxyguanosine (2dG). Control rat mucosa had 8-OHdG values of 1.12 +/- 0.14/10(5) dG (mean +/- SEM, n=11), whereas DMH-treated rats significantly higher values (1.52 +/- 0.14/10(5) dG, n=26, P<0.05). Pretreatment of rats with TR had significantly inhibited DMH-induced oxidative DNA damage 0.99 +/- 0.09/10(5) dG, n=10, P<0.05) and a similar, although less marked, effect was observed with TFu (1.15 +/- 0.19/10(5), n=9, P=0.06). These findings confirm that DMH causes oxidative DNA damage in the colon mucosa of rats and demonstrate that this effect is prevented by the consumption of complex polyphenols from black tea.


Subject(s)
Colonic Neoplasms/chemically induced , DNA Damage/drug effects , Flavonoids , Intestinal Mucosa/drug effects , Phenols/pharmacology , Polymers/pharmacology , Tea/chemistry , 1,2-Dimethylhydrazine/toxicity , 8-Hydroxy-2'-Deoxyguanosine , Alkylating Agents/toxicity , Animals , Antioxidants/pharmacology , Carcinogens/toxicity , Catechin/analogs & derivatives , Catechin/pharmacology , Chromatography, High Pressure Liquid , Colonic Neoplasms/prevention & control , Deoxyguanosine/analogs & derivatives , Deoxyguanosine/analysis , Male , Phytotherapy , Polyphenols , Rats , Rats, Inbred F344 , Tea/therapeutic use
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