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1.
Biomed Res Int ; 2017: 5841805, 2017.
Article in English | MEDLINE | ID: mdl-28691027

ABSTRACT

BACKGROUND: Hand hygiene practices (HHP), as a critical component of infection prevention/control, were investigated among physiotherapists in an Ebola endemic region. METHOD: A standardized instrument was administered to 44 randomly selected physiotherapists (23 males and 21 females), from three tertiary hospitals in Enugu, Nigeria. Fifteen participants (aged 22-59 years) participated in focus group discussions (FGDs) and comprised 19 participants in a subsequent laboratory study. After treatment, the palms/fingers of physiotherapists were swabbed and cultured, then incubated aerobically overnight at 37°C, and examined for microbial growths. An antibiogram of the bacterial isolates was obtained. RESULTS: The majority (34/77.3%) of physiotherapists were aware of the HHP protocol, yet only 15/44.1% rated self-compliance at 71-100%. FGDs identified forgetfulness/inadequate HHP materials/infrastructure as the major barriers to HHP. Staphylococcus aureus were the most prevalent organisms, prior to (8/53.33%) and after (4/26.67%) HPP, while Pseudomonas spp. were acquired thereafter. E. coli were the most antibiotic resistant microbes but were completely removed after HHP. Ciprofloxacin and streptomycin were the most effective antibiotics. CONCLUSION: Poor implementation of HPP was observed due to inadequate materials/infrastructure/poor behavioral orientation. Possibly, some HPP materials were contaminated; hence, new microbes were acquired. Since HPP removed the most antibiotic resistant microbes, it might be more effective in infection control than antibiotic medication.


Subject(s)
Endemic Diseases/statistics & numerical data , Hand Hygiene , Hand/microbiology , Hemorrhagic Fever, Ebola/epidemiology , Physical Therapists , Public Health , Anti-Bacterial Agents/pharmacology , Bacteria/growth & development , Bacteria/isolation & purification , Colony Count, Microbial , Compliance , Female , Focus Groups , Hospitals, Teaching/statistics & numerical data , Humans , Male , Microbial Sensitivity Tests , Nigeria/epidemiology , Tertiary Care Centers
2.
Toxicol Appl Pharmacol ; 154(1): 59-66, 1999 Jan 01.
Article in English | MEDLINE | ID: mdl-9882592

ABSTRACT

Cadmium (Cd) is reported to produce cardiotoxicity at doses and exposure conditions that cause no effect in kidney or liver. The purpose of the present investigation was to examine the cytotoxicity of Cd to neonatal rat cardiomyocytes in primary culture and to elucidate the transport characteristics of Cd in these cells at a nontoxic concentration. Cd concentrations of 0.1 microM and higher that are well tolerated by hepatocytes and renal cortical epithelial cells were toxic to the cardiomyocyte. The plot of initial uptake rate of Cd at various concentrations was nonlinear suggesting that, in addition to simple diffusion, other processes may also be involved. These processes required metabolic energy as pretreatment with dinitrophenol or sodium fluoride inhibited 58 and 59% of the Cd uptake, respectively. The uptake of Cd was also affected by the incubation temperature and lowering the temperature from 37 to 4 degreesC reduced Cd uptake over 30 min by 61%. Cd uptake required interaction with membrane sulfhydryl groups; pretreatment with p-chloromercuribenzenesulfonic acid or mercuric chloride reduced Cd uptake by 46 and 58%, respectively. Cd utilized the transport pathways for calcium (Ca), zinc (Zn), and copper (Cu). Coincubation with 1.26 mM Ca competitively inhibited Cd uptake by 77%. In the presence of Ca, 30 microM Zn or Cu further inhibited Cd accumulation competitively by as much as 63 and 32%, respectively. Cd could enter the cardiomyocytes through Ca channels and Ca channel blocker, verapamil, inhibited up to 76% of Cd uptake. From the above results it can be concluded that Cd is highly toxic to the cardiomyocytes. A majority of Cd enters these cells through transport processes that exist for Ca, Zn, and Cu. The transport processes utilized by Cd are temperature sensitive and dependent on metabolic energy. Furthermore, these involve membrane sulfhydryl groups and include Ca channels.


Subject(s)
Cadmium/metabolism , Cadmium/toxicity , Heart Diseases/chemically induced , Myocardium/metabolism , Animals , Biological Transport , Cadmium/administration & dosage , Calcium/metabolism , Calcium/pharmacology , Cell Death , Cells, Cultured , Copper/metabolism , Copper/pharmacology , Kinetics , Rats , Rats, Sprague-Dawley , Sulfhydryl Reagents/pharmacology , Temperature , Zinc/metabolism , Zinc/pharmacology
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