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2.
Int J Equity Health ; 21(1): 133, 2022 09 13.
Artículo en Inglés | MEDLINE | ID: mdl-36100901

RESUMEN

BACKGROUND: Health inequality monitoring can generate important evidence to inform and motivate changes to policy, programmes and practices. However, the potential of health inequality monitoring practices to quantify inequalities between population subgroups and track progress on the advancement of health equity is under-realized. Capacity strengthening on health inequality monitoring can play an important role in enhancing political will for the generation and use of disaggregated data and for wider adoption of this practice to inform health decision-making. There is a lack of widely available and accessible training materials related to health inequality monitoring that may be used by a range of stakeholders. OBJECTIVE: In this paper, we describe the design, development and implementation of the Health Inequality Monitoring channel on the OpenWHO eLearning platform. We discuss the anticipated impact and potential opportunities for these eLearning courses to contribute to strengthened health inequality monitoring practices. RESULTS: The Health Inequality Monitoring channel on the OpenWHO platform is a self-directed learning environment, designed to meet the immediate learning needs of users. The channel contains three series of courses: health inequality monitoring foundations courses; topic-specific health inequality monitoring courses; and health inequality monitoring skill building courses. Courses are primarily targeted to monitoring and evaluation officers, data analysts, academics and researchers, public health professionals, medical and public health students, and others with a general interest in health data and inequality monitoring. CONCLUSIONS: WHO eLearning courses on health inequality monitoring are addressing the need for capacity strengthening in the collection, analysis and reporting of inequality data. They introduce learners to the foundational concepts, best practices, tools and skills required to conduct health inequality monitoring. The courses on the Health Inequality Monitoring channel demonstrate how technical information can be simplified and presented to broad audiences in a manner that is highly accessible to learners. The Health Inequality Monitoring channel on OpenWHO is an innovative and necessary addition to existing tools and resources to support the advancement of health equity.


Asunto(s)
Instrucción por Computador , Equidad en Salud , Salud Global , Disparidades en el Estado de Salud , Humanos , Salud Pública
3.
Int J Legal Med ; 136(1): 309-317, 2022 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-34613463

RESUMEN

In forensic anthropology, there is an inherent difficulty in estimating the post-mortem interval (PMI). This study aimed to assess whether there is a correlation between changes in the bone mineral component and the PMI estimation. Samples of femur and humerus from 80 identified individuals with known post-mortem interval were analyzed. Infrared spectroscopy in attenuated total reflectance mode (FTIR-ATR) was applied for this analysis, several indices having been obtained from the infrared bands most representative of the bone's relative contents in carbonate and phosphate. Specific relationships between sex/age and PMI were attained: for larger PMIs, there was an increase in the amount of B-type carbonate (BPI), A-type carbonates (API), and in the carbonate/phosphate (C/P) ratio, and a decrease of the crystallinity index (CI) and in the carbonate ratio (C/C). Two particular infrared indices (CI and C/C) were identified as the most suitable for post-mortem interval estimation, especially in females, controlling the effects of sex and age (in the statistical analysis).


Asunto(s)
Antropología Forense , Húmero , Autopsia/métodos , Femenino , Fémur/química , Antropología Forense/métodos , Humanos , Cambios Post Mortem , Espectroscopía Infrarroja por Transformada de Fourier/métodos
4.
West J Emerg Med ; 21(3): 722-726, 2020 Apr 27.
Artículo en Inglés | MEDLINE | ID: mdl-32421525

RESUMEN

INTRODUCTION: A bag valve mask (BVM) is a life saving device used by all levels of health care professionals during resuscitative care. We focus most of our time optimizing the patient's position, firmly securing the mask, and frequency of ventilations. However, despite our best efforts to control these factors, we may still be precipitating harm to the patient. Multiple studies have shown the tidal volumes typically delivered by the adult BVM are often higher than recommended for lung-protective ventilation protocols. In this study we measure and compare the ventilation parameters delivered by the adult and pediatric BVM ventilators. METHODS: A RespiTrainer Advance® adult mannequin was used to simulate a patient. Healthcare providers were directed to manually ventilate an intubated mannequin for two minutes using adult and pediatric sized BVMs. Tidal volume, minute ventilation, peak pressure, and respiration rate was recorded. RESULTS: The adult BVM provided a mean tidal volume of 807.7mL versus the pediatric BVM providing 630.7mL, both of which exceeded the upper threshold of 560mL of tidal volume necessary for lung protective ventilation of an adult male with an ideal body weight of 70kg. The adult BVM exceeded this threshold by 44.2% versus the pediatric BVM's 12.6% with 93% of participants exceeding the maximum threshold with the adult BVM and 82.3% exceeding it with the pediatric BVM. CONCLUSION: The pediatric BVM in our study provided far more consistent and appropriate ventilation parameters for adult patients compared to an adult BVM, but still exceeded the upper limits of lung protective ventilation parameters. The results of this study highlight the potential dangers in using an adult BVM due to increased risk of pulmonary barotrauma. These higher tidal volumes can contribute to lung injury. This study confirms that smaller BVMs may provide safer ventilatory parameters. Future studies should focus on patient-centered outcomes with BVM.


Asunto(s)
Respiración Artificial , Resucitación , Volumen de Ventilación Pulmonar , Adulto , Niño , Humanos , Lesión Pulmonar/etiología , Lesión Pulmonar/prevención & control , Maniquíes , Respiración Artificial/instrumentación , Respiración Artificial/métodos , Respiración Artificial/normas , Resucitación/instrumentación , Resucitación/métodos , Resucitación/normas , Entrenamiento Simulado/métodos , Desarrollo de Personal , Ventiladores Mecánicos/normas
5.
Clin Rehabil ; 29(1): 59-68, 2015 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-24965957

RESUMEN

OBJECTIVE: To assess the effectiveness of pilates method on patients with chronic non-specific low back pain (LBP). METHOD: A randomized controlled trial was carried out in sixty patients with a diagnosis of chronic non-specific LBP. Patients were randomly assigned to one of two groups: Experimental Group (EG) that maintained medication treatment with use of NSAID and underwent treatment with the pilates method and Control Group (CG) that continue medication treatment with use of NSAID and did not undergo any other intervention. A blinded assessor performed all evaluations at baseline (T0), after 45, 90, and 180 days (T45, T90 and T180) for: pain (VAS), function (Roland Morris questionnaire), quality of life (SF-36), satisfaction with treatment (Likert scale), flexibility (sit and reach test) and NSAID intake. RESULTS: The groups were homogeneous at baseline. Statistical differences favoring the EG were found with regard to pain (P < 0.001), function (P < 0.001) and the quality of life domains of functional capacity (P < 0.046), pain (P < 0.010) and vitality (P < 0.029). Statistical differences were also found between groups regarding the use of pain medication at T45, T90 and T180 (P < 0.010), with the EG taking fewer NSAIDs than the CG. CONCLUSIONS: The pilates method can be used by patients with LBP to improve pain, function and aspects related to quality of life (functional capacity, pain and vitality). Moreover, this method has no harmful effects on such patients.


Asunto(s)
Actividades Cotidianas , Diclofenaco/administración & dosificación , Técnicas de Ejercicio con Movimientos/métodos , Dolor de la Región Lumbar/terapia , Calidad de Vida , Análisis de Varianza , Antiinflamatorios no Esteroideos/administración & dosificación , Antiinflamatorios no Esteroideos/uso terapéutico , Actitud del Personal de Salud , Diclofenaco/uso terapéutico , Femenino , Humanos , Dolor de la Región Lumbar/tratamiento farmacológico , Masculino , Persona de Mediana Edad , Dimensión del Dolor/métodos , Dimensión del Dolor/estadística & datos numéricos , Satisfacción del Paciente/estadística & datos numéricos , Método Simple Ciego , Estadísticas no Paramétricas
6.
Acupunct Med ; 32(2): 109-15, 2014 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-24316509

RESUMEN

OBJECTIVE: To assess the efficacy of Yamamoto's acupuncture method on pain, drug intake, functional capacity and quality of life for the treatment of acute non-specific low back pain (ANLBP). METHODS: A prospective, randomised, parallel-group, double-blind, placebo-controlled trial was performed in 80 men and women with ANLBP who were randomly assigned to five acupuncture sessions (intervention group (IG), n=40) and to five non-penetrating acupuncture sessions (sham group (SG), n=40). Patients were evaluated at baseline and at 3, 7, 14, 21 and 28 days. The measurements used were: visual analogue scale (VAS) for cumulative pain (before intervention, VAS1) and immediate pain (after intervention, VAS2); function (Roland-Morris Disability Questionnaire (RM)); quality of life (SF-36); improvement rating; and number of anti-inflammatory tablets taken. The primary endpoint was a decrease of at least 2 cm in VAS1. RESULTS: Pain VAS improved significantly in the IG from day 14 onwards compared with the SG, but the difference did not reach the prespecified clinically relevant value of 2 cm. The IG was significantly superior to the SG in the following outcomes: cumulative pain, function, pain (SF-36) and vitality (SF-36) at days 14, 21 and 28 (p<0.05); limitation in physical aspects (SF-36) at all times (p=0.007 and p=0.02); and functional capacity (SF-36) at days 21 and 28 (p<0.05). The IG also took significantly fewer anti-inflammatory tablets than the SG (p=0.004) at all evaluation times and the improvement rating was better than the SG (p<0.001). CONCLUSIONS: Yamamoto's new scalp acupuncture was more effective than sham treatment with regard to decrease in pain and anti-inflammatory intake as well as improving functional status and quality of life for patients with ANLBP. CLINICALTRIALSGOV: NCT 01124955.


Asunto(s)
Terapia por Acupuntura , Dolor Agudo/terapia , Dolor de la Región Lumbar/terapia , Puntos de Acupuntura , Adolescente , Adulto , Anciano , Método Doble Ciego , Femenino , Humanos , Masculino , Persona de Mediana Edad , Resultado del Tratamiento , Adulto Joven
7.
Prehosp Disaster Med ; 25(4): 335-9, 2010.
Artículo en Inglés | MEDLINE | ID: mdl-20845321

RESUMEN

OBJECTIVE: The objective of this study was to evaluate the time saved by usage of lights and siren (L&S) during emergency medical transport and measure the total number of time-critical hospital interventions gained by this time difference. METHODS: A retrospective study was performed of all advanced life support (ALS) transports using lights and siren to this university emergency department during a three-week period. Consecutive times were measured for 112 transports and compared with measured transport times for a personal vehicle traveling the same day of the week and time of day without lights and siren. The time-critical hospital interventions are defined as procedures or treatments that could not be performed in the prehospital setting requiring a physician. The project assessed whether the patients received the hospital interventions within the average time saved using lights and siren transport. RESULTS: The average difference in time with versus without L&S was -2.62 minutes (95% CI: -2.60- -2.63, paired t-test p<0.0001). The average transport time with L&S was 14.5±7.9 minutes (min) (1 standard deviation/minute (min), range=1-36 min.). The average transport time without L&S was 17.1±8.3 min (range=1-40 min). Of the 112 charts evaluated, five patients (4.5%) received time-critical hospital interventions. No patients received time-critical interventions within the time saved by utilizing lights and siren. Longer distances did not result in time saved with lights and siren. CONCLUSIONS: Limiting lights and siren use to the patients requiring hospital interventions will decrease the risks of injury and death, while adding the benefit of time saved in these critical patients.


Asunto(s)
Apoyo Vital Cardíaco Avanzado , Ambulancias/normas , Servicio de Urgencia en Hospital , Equipos de Seguridad , Humanos , Iluminación , Ruido , Estudios Retrospectivos , Factores de Tiempo , Transporte de Pacientes
8.
Prehosp Disaster Med ; 25(4): 341-5, 2010.
Artículo en Inglés | MEDLINE | ID: mdl-20845322

RESUMEN

OBJECTIVE: A rapid sequence intubation (RSI) method was introduced to a university-based emergency medical services (EMS) system. This is a report of the initial experience with the first 50 patients in a unique, two-tiered, two advanced life support (ALS) providers system. METHODS: The data were evaluated prospectively after an extensive RSI training period, consisting of didactic information and skills performance. Fifty consecutive patient records that documented the procedure were abstracted. Data abstracted included end-tidal CO2, heart rate, blood pressure, and pulse oximetry at various time intervals. Intubation success rates and number of attempts were documented. The consistency of proper documentation also was noted on patient care records. RESULTS: No differences were noted in heart rate prior to RSI and one and five minutes after the RSI procedure was begun. No differences in blood pressure at one and five minutes were noted. Statistically significant improvements were found in pulse oximetry comparing prior to RSI and one minute after (p<0.001; 95% CI: 3.15-11.41) as well as prior to RSI and five minutes after RSI was started (p<0.0002; 95% CI=4.60-13.33). No differences were observed in end-tidal CO2 at one and five minutes. Overall intubation success rate was 96%, with 82% on first attempt and 92% on two or less attempts. Documentation for individual vitals was consistently <75%. CONCLUSIONS: Patients had no significant worsening of vital signs during the RSI procedure and mild improvement in pulse oximetry. Intubation success rates were consistent with national averages. Proper documentation was lacking in more than one quarter of the charts. These data add to a body of literature that raises further concerns regarding prehospital RSI.


Asunto(s)
Servicios Médicos de Urgencia/métodos , Intubación Intratraqueal/métodos , Succinilcolina/administración & dosificación , Auxiliares de Urgencia , Humanos , Fármacos Neuromusculares Despolarizantes/administración & dosificación , Estudios Prospectivos , Garantía de la Calidad de Atención de Salud/métodos , Resultado del Tratamiento
9.
Postgrad Med ; 122(4): 144-57, 2010 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-20675977

RESUMEN

Knowledge of sudden cardiac death in young athletes is imperative for all physicians and allied health professionals. The complete differential diagnosis of a young patient with sudden cardiac arrest will result in proper work-up and treatment. In this article, we review several etiologies of sudden cardiac death, including hypertrophic cardiomyopathy, arrhythmogenic right ventricular cardiomyopathy, Wolff-Parkinson-White syndrome, long QT syndrome, Brugada syndrome, and commotio cordis. Clinical findings, work-up, treatment, long-term management, and athlete preparticipation screening guidelines are discussed.


Asunto(s)
Atletas , Muerte Súbita Cardíaca/etiología , Adulto , Reanimación Cardiopulmonar , Muerte Súbita Cardíaca/epidemiología , Muerte Súbita Cardíaca/prevención & control , Electrocardiografía , Humanos , Incidencia , Tamizaje Masivo , Factores de Riesgo , Estados Unidos/epidemiología
10.
Acad Emerg Med ; 17(6): 631-7, 2010 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-20624143

RESUMEN

OBJECTIVES: Pharmaceutical manufacturers recommend refrigerating succinylcholine at a temperature range of 2-8 degrees C. With widespread use of prehospital succinylcholine on ambulances without refrigeration, it is important to understand the stability of this drug. Using mass spectrometry, this study investigated the degradation of the succinylcholine compound before and after its exposure to ambulance cabin temperatures, while removing light exposure. A 10% degradation threshold was set as not appropriate for human use, in accordance with U.S. Food and Drug Administration guidelines. METHODS: The study used 17 vials of succinylcholine sealed with duct tape in light-resistant bags. The bags were placed in climate controlled compartments in two ambulances: one stationed in a garage and the other stationed outdoors. Mass spectrometry analysis was used to examine drug degradation at Time 0, the 14th day of the first month, and monthly from Time 0 to 7 months. RESULTS: The degradation products of succinyl monocholine (SMC) and choline are already present at Day 0. Ten percent degradation was achieved at approximately 90 days into the experiment. Temperature in the ambulance climate controlled compartment was 70 degrees F, with a range from 56 to 89 degrees F during the 6-month time period. CONCLUSIONS: Identifiable breakdown fragments of succinylcholine have been identified using mass spectrometry with fresh drug upon receipt from the manufacturer. Ten percent degradation was not observed until approximately 90 days after being placed on ambulances. Temperature variations did not significantly contribute to degradation of succinylcholine, and it is safe for injection until approximately 90 days in similar climates.


Asunto(s)
Fármacos Neuromusculares Despolarizantes/química , Succinilcolina/química , Estabilidad de Medicamentos , Almacenaje de Medicamentos , Servicios Médicos de Urgencia , Ambiente Controlado , Humanos , Espectrometría de Masas , Estudios Prospectivos , Temperatura
11.
Am J Emerg Med ; 28(5): 552-60, 2010 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-20579549

RESUMEN

OBJECTIVE: This article models use of emergency medical services (EMS) within a defined geographical area. Our goal was to develop an original quantitative method to delineate the need for EMS units within a geographical population. METHODS: Use of the EMS system within 11 municipalities was analyzed in 2007. The geospatial distributions of interventions during this year were examined, as well as the population dynamics of the region. A statistical model to determine the probability of an individual within the call area requiring an intervention was proposed using weighted population statistics and the application of an intervention probability. RESULTS: The observed interventional probability increased exponentially with age, notably after the age of 75. Areas with higher proportions of elderly residents had substantially higher rates of intervention and EMS use. Municipality H had the largest age-group of 20 to 24 years with an intervention probability of 0.34% (95% confidence interval [CI], 0.24-0.44), their more than 85-year age-group also had the largest intervention probability of 19.54% (95% CI, 15.60-23.48). CONCLUSIONS: Contrary to current practice patterns of placing paramedic units in regions of greatest population density, we established a formula based on population vs intervention probability. We found the actual numbers of interventions performed are not dependent solely on population size but also are affected by the age of the population being served. This is particularly relevant to growing elderly communities. This determination will aid in the disbursement of limited prehospital resources in regions by improving availability of EMS personnel.


Asunto(s)
Urgencias Médicas/epidemiología , Servicios Médicos de Urgencia/provisión & distribución , Necesidades y Demandas de Servicios de Salud , Adulto , Factores de Edad , Anciano , Anciano de 80 o más Años , Ciudades/epidemiología , Servicios Médicos de Urgencia/métodos , Auxiliares de Urgencia/provisión & distribución , Humanos , Persona de Mediana Edad , Modelos Estadísticos , Densidad de Población , Dinámica Poblacional , Probabilidad , Adulto Joven
12.
Emerg Med J ; 27(2): 147-50, 2010 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-20156875

RESUMEN

OBJECTIVES: The objective of this study was to survey medical students for a measurable opinion or knowledge increase in prehospital care after a fourth-year clerkship in emergency medicine (EM). The goal of the mandatory prehospital care aspect of the clerkship was twofold: to diminish the prehospital knowledge gap in medical school by teaching students about prehospital protocols and disaster medicine and to increase student interest. METHODS: The study setting was within a university-based academic EM department with a prehospital system of 250 prehospital personnel. Data were collected from two similar questionnaires administered pre- and post-rotation to 49 fourth-year medical students. Statistical analyses were applied to collected data to quantify the changes of opinion and knowledge. Questions used a Likert five-point Scale. RESULTS: The data verified the improvement of students' knowledge in multiple areas of assessment. Greater than 35% opinion change (two points on the Likert Scale) was found in areas of prehospital care, 911 dispatch and education differences in prehospital providers (all p<0.0001; 95% CI 0.90 to 1.02, 0.66 to 0.90 and 0.66 to 0.90, respectively). Greater than 35% opinion change was also found in understanding triage (p=0.03; 95% CI 0.29 to 0.58) and general teaching of prehospital care, fellowship opportunities and use of a monitor/defibrillator (p<0.0001, p<0.0001 and p=0.04, respectively). CONCLUSIONS: We found medical students developed a significantly improved understanding of prehospital care. Without extraordinary effort, academic emergency departments could easily include a significant experience and education within fourth-year EM clerkships.


Asunto(s)
Prácticas Clínicas , Servicios Médicos de Urgencia , Medicina de Emergencia/educación , Centros Médicos Académicos , Curriculum , Humanos , New Jersey , Estudiantes de Medicina
13.
Cases J ; 2: 7420, 2009 Jul 10.
Artículo en Inglés | MEDLINE | ID: mdl-19829959

RESUMEN

INTRODUCTION: This is the case of a rare and regional disease not often considered in the immunocompromised patient presenting with a chief complaint of fever. CASE PRESENTATION: A 37-year-old immunocompromised Indian woman presented with a chief complaint of fever, in the absence of localizing signs and symptoms, from an area endemic to Babesia microti. CONCLUSIONS: Our patient's case is instructive in that Babesiosis and other arthropod born illnesses should be considered in immunocompromised patients presenting with fever in the absence of localizing signs or symptoms. This is especially true when he or she presents from an area with known endemic disease. While the management of fever in immunocompromised patients is largely standardized, considering Babesiosis from the beginning may prompt early investigation of a blood smear, which has the potential to alert the emergency department physician to Babesiosis. In addition, considering the disease from the outset has the potential to accelerate administration of the appropriate antimicrobial therapy and thus prevent unnecessary morbidity and possible mortality.

14.
Postgrad Med ; 121(2): 163-7, 2009 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-19332974

RESUMEN

BACKGROUND: OxyContin (controlled-release oxycodone hydrochloride) (Purdue Pharma, Stamford, CT) was approved in 1995 by the US Food and Drug Administration (FDA) for moderate-to-severe chronic pain. Crushing and snorting the delayed-release tablets results in a rapid release of the drug, increased absorption, and high peak serum concentrations. The propensity for addiction to OxyContin and the trend of increased prescription drug abuse have made it imperative for physicians and health care providers to recognize the clinical presentation of overdose and know how to manage associated complications. OBJECTIVES: In this review of OxyContin, we discuss current trends in its abuse and the clinical presentation of overdose. We review the specific effects of the drug on body systems and the recognition of symptomatology, differential diagnosis, and management. DISCUSSION: Many of the clinical findings in acute opioid overdoses are nonspecific, making diagnosis difficult. OxyContin overdose presents with a typical opiate toxidrome, including decreased respirations, miosis, hypothermia, bradycardia, hypotension, and altered mental status. The presence of coingestants can cloud the clinical picture. If OxyContin overdose is suspected, early ventilation and oxygenation should be administered, which is generally sufficient to prevent death. Even in the absence of a confirmation, cautious administration of naloxone--the opiate receptor antagonist and antidote for opioid overdoses--may have both diagnostic and therapeutic effects. SUMMARY: With increasing rates of prescription drug abuse, OxyContin will continue to present challenges to physicians and health care providers. Physicians should be aware of potential patients who are seeking OxyContin for recreational use.


Asunto(s)
Analgésicos Opioides/efectos adversos , Trastornos Relacionados con Opioides/diagnóstico , Oxicodona/efectos adversos , Analgésicos Opioides/farmacocinética , Analgésicos Opioides/envenenamiento , Preparaciones de Acción Retardada , Diagnóstico Diferencial , Sobredosis de Droga/diagnóstico , Sobredosis de Droga/terapia , Humanos , Oxicodona/farmacocinética , Oxicodona/envenenamiento
15.
Prehosp Emerg Care ; 13(1): 71-4, 2009.
Artículo en Inglés | MEDLINE | ID: mdl-19145528

RESUMEN

OBJECTIVE: The investigation seeks to determine the prevalence of methicillin-resistant Staphylococcus aureus (MRSA) on the stethoscopes of emergency medical services (EMS) providers. While stethoscopes are known fomites for MRSA, the prevalence of MRSA in the prehospital setting is not well documented in the literature. METHODS: This was a prospective, observational cohort study of 50 stethoscopes provided by consecutive, consenting EMS providers at our academic emergency department (ED). Stethoscopes were swabbed with saline culture applicators and samples were cultured on a commercial MRSA test kit containing mannitol salt agar with oxacillin. After 72 hours of incubation at 37 degrees C, two emergency physicians and one microbiologist analyzed the plates independently. MRSA colonization was recorded as positive if all three reviewers agreed that colonization had occurred. RESULTS: Of 50 stethoscopes, 16 had MRSA colonization, and 16 (32%) EMS professionals had no recollection of when their stethoscopes had been cleaned last. Reported length of time since last cleaning was grouped into six categories: one to seven days, eight to 14 days, 15 to 30 days, 31 to 180 days, 181 days to 365 days, and unknown. The median time frame reported since the last cleaning was one to seven days. In the model, an increase from one time category to the next increased the odds of MRSA colonization by 1.86 (odds ratio = 1.86, p = 0.038). CONCLUSIONS: In this ED setting, MRSA was found on approximately one in three stethoscopes of EMS professionals. A longer length of time since the last stethoscope cleaning increased the odds of MRSA colonization.


Asunto(s)
Auxiliares de Urgencia , Contaminación de Equipos/estadística & datos numéricos , Staphylococcus aureus Resistente a Meticilina/aislamiento & purificación , Estetoscopios/microbiología , Estudios de Cohortes , Recuento de Colonia Microbiana , Infección Hospitalaria/etiología , Descontaminación/estadística & datos numéricos , Humanos , New Jersey/epidemiología , Prevalencia
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