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1.
Int J Occup Environ Health ; 18(4): 307-11, 2012.
Artículo en Inglés | MEDLINE | ID: mdl-23433291

RESUMEN

INTRODUCTION: A disparate number of occupational exposures to bloodborne pathogens occur in low-income countries where disease prevalence is high and healthcare provider-per-population ratios are low. METHODS: In an effort to highlight the important role of healthcare worker safety in surgical capacity building in Rwanda, we measured self-reported presence of safety materials and compliance with personal protective equipment in the operating theatre as part of a nationwide survey to characterize emergency and essential surgical capacity in all government hospitals. RESULTS: We surveyed 44 hospitals. While staff report general availability of safe disposal of sharps and hazardous waste, presence of and compliance with eye protection was lacking. Staff were cognizant of prevention measures such as double-gloving and 'safe receptacles', as well as hospital policies for post-exposure prophylaxis for HIV following needlesticks, but there was little awareness of hepatitis exposure. CONCLUSIONS: Healthcare worker safety should be a key component of hospital-level surgical capacity.


Asunto(s)
Personal de Salud , Exposición Profesional/prevención & control , Quirófanos/organización & administración , Equipos de Seguridad/estadística & datos numéricos , Administración de la Seguridad/organización & administración , Patógenos Transmitidos por la Sangre , Infecciones por VIH/etiología , Infecciones por VIH/prevención & control , Hepatitis B/etiología , Hepatitis B/prevención & control , Hepatitis C/etiología , Hepatitis C/prevención & control , Humanos , Eliminación de Residuos Sanitarios/métodos , Eliminación de Residuos Sanitarios/estadística & datos numéricos , Lesiones por Pinchazo de Aguja/prevención & control , Exposición Profesional/estadística & datos numéricos , Quirófanos/estadística & datos numéricos , Políticas , Profilaxis Posexposición/estadística & datos numéricos , Rwanda , Administración de la Seguridad/estadística & datos numéricos
3.
Cancer Epidemiol Biomarkers Prev ; 15(5): 840-55, 2006 May.
Artículo en Inglés | MEDLINE | ID: mdl-16702359

RESUMEN

PURPOSE: Individuals and families dealing with the possibility of hereditary cancer risk face numerous decisions, including whether to obtain genetic testing. The purpose of this article is to determine what is known about the rate at which people obtain cancer genetic testing. METHODS: Using MEDLINE, CINAHL, and PSYCHINFO plus reviewing reference lists of relevant articles, we identified 40 studies in May 2002 that addressed breast cancer-related decisions, enrolled adult participants, were published in 1990 or more recently, were peer-reviewed primary clinical studies, addressed genetic testing either alone or in combination with genetic counseling, and reported rates at which participants showed interest in and/or underwent cancer genetic testing. Information regarding study design, participants, and genetic testing uptake rates was recorded. Each article was reviewed for methodologic quality using a flexible quality review system applicable to all study types. RESULTS: Of the 40 studies, 25 provided information about hypothetical genetic testing decisions, 14 about real decisions, and 1 about both. Mean hypothetical uptake was 66% (range, 20-96%) and real uptake was 59% (range, 25-96%). Multivariate logistic regression analyses found that decision type (real/hypothetical), personal and family history of breast cancer, and variability in sampling strategy, recruitment setting, and criteria for real and hypothetical uptake were independently associated with uptake. Our systematic review identified additional explanations for uptake variability (investigator influences, small sample sizes, variability in target populations, lack of clearly described sampling strategies, sampling methods open to bias, and variability in reporting associated risk factors). CONCLUSION: In addition to clinical characteristics, research methodologic issues are likely to be major determinants of variability in published breast cancer genetic testing uptake rates. An understanding of these issues will clarify to clinicians why their clinical experience may not be congruent with published rates and help guide future research.


Asunto(s)
Neoplasias de la Mama/genética , Toma de Decisiones , Predisposición Genética a la Enfermedad , Pruebas Genéticas/estadística & datos numéricos , Adulto , Femenino , Asesoramiento Genético , Investigación Genética , Humanos , Modelos Logísticos
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