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2.
J Clin Sleep Med ; 3(7): 700-5, 2007 Dec 15.
Artigo em Inglês | MEDLINE | ID: mdl-18198803

RESUMO

RATIONALE: The treatment of choice for obstructive sleep apnea (OSA) is nasal continuous positive airway pressure (nCPAP) during sleep, but dryness of the upper airway compromises compliance. Heated humidifiers may mitigate such noncompliance; however, recent observations suggest that their use, particularly if not cleaned, increases the risk of respiratory infections. Humidifier water may be contaminated, but the long-held view that passive humidifiers cannot aerosolize water may obscure the perception of risk of infection. OBJECTIVES: This study challenges the long-held view that "passover" humidifiers do not aerosolize water. With such evidence, this study characterizes the performance of filters to reduce the potential risk of contamination. METHODS: Heated humidifier water contaminated with bacteria was studied under conditions simulating week-long use of nCPAP for OSA. RESULTS: Bacteria were recovered in 9 of 11 tests from the breathing tubes of CPAP devices fitted with heated humidifiers with water contaminated with Brevundimonas diminuta or Serratia marcescens. Recoverable bacteria ranged from tens to thousands of colony forming units when tested at air flow rates of 60 liters per minute for 90 minutes. Neither organism was recovered from the circuit tubing when a hydrophobic breathing-circuit filter was positioned between the humidifier and face-mask tubing with a commercially available nCPAP machine tested under simulated-use conditions. CONCLUSION: Data suggest that patients with OSA being treated with nCPAP fitted with humidifiers may be aerosolizing bacteria, putting them at risk for developing respiratory infections and that the use of a hydrophobic filter may attenuate the passage of microbes from contaminated humidifier water.


Assuntos
Infecções Bacterianas/prevenção & controle , Pressão Positiva Contínua nas Vias Aéreas/instrumentação , Umidade , Filtros Microporos , Infecções Respiratórias/transmissão , Microbiologia da Água , Aerossóis , Infecções Bacterianas/microbiologia , Técnicas Bacteriológicas , Caulobacteraceae/crescimento & desenvolvimento , Contagem de Colônia Microbiana , Ensaio de Unidades Formadoras de Colônias , Desenho de Equipamento , Calefação , Humanos , Infecções Respiratórias/microbiologia , Infecções Respiratórias/prevenção & controle , Serratia marcescens/crescimento & desenvolvimento
3.
Am J Infect Control ; 33(5 Suppl 1): S1-19, 2005 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-15940112

RESUMO

Cholera, hepatitis and typhoid are well-recognized water-borne illnesses that take the lives of many every year in areas of uncontrollable flood, but far less attention is afforded to the allegedly safe potable water in affluent nations and the presumed healthful quality of water in communities and hospitals. Recent literature, however, points to increasing awareness of serious clinical sequelae particularly experienced by immunocompromised patients at high risk for disease and death from exposure to water-borne microbes in hospitals. This review reflects the literature indicting hospital water as an important source for nosocomial infections, examines patient populations at greatest risk, uncovers examples of failures in remedial water treatment methods and the reasons for them, and introduces point-of-use water filtration as a practical alternative or complementary component of an infection control strategy that may reduce the risk of nosocomial infections.


Assuntos
Infecção Hospitalar/prevenção & controle , Filtração/instrumentação , Controle de Infecções/instrumentação , Microbiologia da Água , Biofilmes , Hospitais , Humanos , Legionelose/prevenção & controle , Fatores de Risco
4.
Transfusion ; 45(6): 984-93, 2005 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-15934998

RESUMO

BACKGROUND: An enhanced bacterial detection system (Pall eBDS) was developed that distinguishes itself from its predecessor (Pall BDS) by removal of the platelet (PLT)-retaining filter allowing for optimal bacterial transfer, modification of the culture tablet to reduce the confounding effects of respiring PLTs while enhancing bacterial growth, and facilitation of nutrients and gas exchange by agitating the sample pouch during incubation at 35 degrees C. The objective was to evaluate the performance of the new eBDS. STUDY DESIGN AND METHODS: Leukoreduced whole blood-derived PLT concentrates (LR-PCs) and LR single-donor PLTs (LR-SDPs) were inoculated with 1 to 15 colony-forming units (CFUs) of bacteria per mL in studies of each of 10 bacterial species associated with fatal transfusion-transmitted bacterial infection. Immediately after inoculation and after 24 hours of storage at 22 degrees C, samples of inoculated LR-PCs were aseptically transferred into the eBDS pouches. Pouches were then incubated for 24 hours at 35 degrees C with agitation and oxygen concentration was then measured. RESULTS: Median inoculation levels ranged from 5 to 13 CFUs per mL for each species studied. No significant differences in oxygen concentration were found when comparing LR-PCs with LR-SDPs. When sampling occurred from the PLTs 24 hours after inoculation, all 280 cases (24-33 replicates of each species) were detected as contaminated by the device (100% sensitivity). No false-positives were obtained with 713 uninoculated PLT units. CONCLUSIONS: The eBDS demonstrated improved detection sensitivity in the range of 1 to 15 CFUs per mL with no observed false-positives compared to the original BDS (detection range 100 to 500 CFUs/mL) with no false-positives.


Assuntos
Bactérias/isolamento & purificação , Infecções Bacterianas/prevenção & controle , Técnicas Bacteriológicas/instrumentação , Técnicas Bacteriológicas/métodos , Consumo de Oxigênio , Infecções Bacterianas/transmissão , Plaquetas/microbiologia , Estudos de Avaliação como Assunto , Cinética , Leucócitos/citologia , Contagem de Plaquetas , Sensibilidade e Especificidade , Staphylococcus , Fatores de Tempo
5.
Appl Environ Microbiol ; 68(4): 1548-55, 2002 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-11916667

RESUMO

Bacterial populations inhabiting ultrapure water (UPW) systems were investigated. The analyzed UPW systems included pilot scale, bench scale, and full size UPW plants employed in the semiconductor and other industries. Bacteria present in the polishing loop of the UPW systems were enumerated by both plate counts and epifluorescence microscopy. Assessment of bacterial presence in UPW by epifluorescence microscopy (cyanotolyl tetrazolium chloride [CTC] and DAPI [4',6'-diamidino-2-phenylindole] staining) showed significantly higher numbers (10 to 100 times more bacterial cells were detected) than that determined by plate counts. A considerable proportion of the bacteria present in UPW (50 to 90%) were cells that did not give a positive signal with CTC stain. Bacteria isolated from the UPW systems were mostly gram negative, and several groups seem to be indigenous for all of the UPW production systems studied. These included Ralstonia pickettii, Bradyrhizobium sp., Pseudomonas saccharophilia, and Stenotrophomonas strains. These bacteria constituted a significant part of the total number of isolated strains (>or=20%). Two sets of primers specific to R. pickettii and Bradyrhizobium sp. were designed and successfully used for the detection of the corresponding bacteria in the concentrated UPW samples. Unexpectedly, nifH gene sequences were found in Bradyrhizobium sp. and some P. saccharophilia strains isolated from UPW. The widespread use of nitrogen gas in UPW plants may be associated with the presence of nitrogen-fixing genes in these bacteria.


Assuntos
Contaminação de Equipamentos , Bactérias Gram-Negativas/classificação , Microbiologia da Água , Purificação da Água/métodos , Abastecimento de Água , Contagem de Colônia Microbiana , Genes de RNAr , Bactérias Gram-Negativas/genética , Bactérias Gram-Negativas/isolamento & purificação , Indústrias , Microscopia de Fluorescência , Dados de Sequência Molecular , Oxirredutases/genética , Filogenia , Reação em Cadeia da Polimerase , RNA Ribossômico 16S/genética , Semicondutores , Análise de Sequência de DNA , Universidades , Purificação da Água/instrumentação
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