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        <title>BMC Emergency Medicine - Latest Articles</title>
        <link>http://www.biomedcentral.com/bmcemergmed/</link>
        <description>The latest research articles published by BMC Emergency Medicine</description>
        <dc:date>2013-04-22T00:00:00Z</dc:date>
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                                <rdf:li rdf:resource="http://www.biomedcentral.com/1471-227X/13/8" />
                                <rdf:li rdf:resource="http://www.biomedcentral.com/1471-227X/13/7" />
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                                <rdf:li rdf:resource="http://www.biomedcentral.com/1471-227X/12/19" />
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        <item rdf:about="http://www.biomedcentral.com/1471-227X/13/8">
        <title>Impact of a stress coping strategy on perceived stress levels and performance during a simulated cardiopulmonary resuscitation: a randomized controlled trial</title>
        <description>Background:
Cardiopulmonary resuscitation (CPR) causes significant stress for the rescuers which may cause deficiencies in attention and increase distractibility. This may lead to misjudgements of priorities and delays in CPR performance, which may further increase mental stress (vicious cycle). This study assessed the impact of a task-focusing strategy on perceived stress levels and performance during a simulated CPR scenario.
Methods:
This prospective, randomized-controlled trial was conducted at the simulator-center of the University Hospital Basel, Switzerland. A total of 124 volunteer medical students were randomized to receive a 10 minute instruction to cope with stress by loudly posing two task-focusing questions (&#8220;what is the patient&#8217;s condition?&#8221;, &#8220;what immediate action is needed?&#8221;) when feeling overwhelmed by stress (intervention group) or a control group. The primary outcome was the perceived levels of stress and feeling overwhelmed (stress/overload); secondary outcomes were hands-on time, time to start CPR and number of leadership statements.
Results:
Participants in the intervention group reported significantly less stress/overload levels compared to the control group (mean difference: -0.6 (95% CI &#8722;1.3, -0.1), p=0.04). Higher stress/overload was associated with less hands-on time. Leadership statements did not differ between groups, but the number of leadership statements did relate to performance. Hands-on time was longer in the intervention- group, but the difference was not statistically significant (difference 5.5 (95% CI &#8722;3.1, 14.2), p=0.2); there were no differences in time to start CPR (difference &#8722;1.4 (95% CI &#8722;8.4, 5.7), p=0.71).
Conclusions:
A brief stress-coping strategy moderately decreased perceived stress without significantly affecting performance in a simulated CPR. Further studies should investigate more intense interventions for reducing stress.Trial registrationNCT01645566</description>
        <link>http://www.biomedcentral.com/1471-227X/13/8</link>
                <dc:creator>Sabina Hunziker</dc:creator>
                <dc:creator>Simona Pagani</dc:creator>
                <dc:creator>Katrin Fasler</dc:creator>
                <dc:creator>Franziska Tschan</dc:creator>
                <dc:creator>Norbert Semmer</dc:creator>
                <dc:creator>Stephan Marsch</dc:creator>
                <dc:source>BMC Emergency Medicine 2013, null:8</dc:source>
        <dc:date>2013-04-22T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1471-227X-13-8</dc:identifier>
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                <prism:publicationName>BMC Emergency Medicine</prism:publicationName>
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        <prism:startingPage>8</prism:startingPage>
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        <item rdf:about="http://www.biomedcentral.com/1471-227X/13/7">
        <title>Over-prescribing of antibiotics and imaging in the management of uncomplicated URIs in emergency departments</title>
        <description>Background:
Unnecessary use of resources for common illnesses has substantial effect on patient care and costs. Evidence-based guidelines do not recommend antibiotics or imaging for uncomplicated upper respiratory infections (URIs). The objective of the current study was to examine medical care providers&#8217; compliance with guidelines in treating uncomplicated URIs in emergency departments (EDs) in the US.
Methods:
Nationally representative data from the NHAMCS 2007 and 2008 were used. Uncomplicated URIs were identified through ICD-9 codes of nasopharyngitis, laryngitis, bronchitis, URI not otherwise specified and influenza involving upper respiratory tract. Exclusion criteria were concurrent comorbidities, follow-up visits, and age&#8201;&lt;&#8201;18 or &gt;64&#8201;years. Most frequently prescribed classes of antibiotics were identified. Multivariate analyses were conducted to identify the factors associated with the prescribing of antibiotics and use of imaging studies.
Results:
In 2007 and 2008, there were 2.2 million adult uncomplicated URI visits without any other concurrent diagnoses in EDs in the US. Approximately 52% were given antibiotic prescriptions, over one-third of which were macrolides, and nearly half of the visits performed imaging studies. About 51% had a diagnosis of bronchitis, 35% URI NOS, 9% nasopharyngitis, laryngitis or influenza, and 4% multiple URI diagnoses. The diagnosis of bronchitis, fever at presentation, older ages, male gender, longer waiting time, and metropolitan areas were associated with a greater likelihood of prescribing antibiotics or imaging studies, controlling for confounding factors.
Conclusion:
Despite the recommendations and campaign efforts by the CDC and many medical associations, the prescribing of antibiotics in treating uncomplicated URIs in the EDs remains prevalent. Furthermore, overutilization of imaging studies is prevalent. Changes at levels of health care system and hospitals are needed to avoid unnecessary resource utilization. In addition, further patient education about antibiotic use in the community may greatly facilitate the transition out of an antibiotic-dependent consumer culture.</description>
        <link>http://www.biomedcentral.com/1471-227X/13/7</link>
                <dc:creator>K Xu</dc:creator>
                <dc:creator>Daniel Roberts</dc:creator>
                <dc:creator>Irvin Sulapas</dc:creator>
                <dc:creator>Omar Martinez</dc:creator>
                <dc:creator>Justin Berk</dc:creator>
                <dc:creator>John Baldwin</dc:creator>
                <dc:source>BMC Emergency Medicine 2013, null:7</dc:source>
        <dc:date>2013-04-17T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1471-227X-13-7</dc:identifier>
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                <prism:publicationName>BMC Emergency Medicine</prism:publicationName>
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        <prism:startingPage>7</prism:startingPage>
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        <item rdf:about="http://www.biomedcentral.com/1471-227X/13/6">
        <title>Epidemiology of noninvasive mechanical ventilation in acute respiratory failure - a retrospective population-based study</title>
        <description>Background:
Noninvasive mechanical ventilation (NIV) is a front-line therapy for the management of acute respiratory failure (ARF) in the intensive care units. However, the data on factors and outcomes associated with the use of NIV in ARF patients is lacking. Therefore, we aimed to determine the utilization of NIV for ARF in a population-based study.
Methods:
We conducted a populated-based retrospective cohort study, where in all consecutively admitted adults (&#8805;18&#8201;years) with ARF from Olmsted County, Rochester, MN, at the Mayo Clinic medical and surgical ICUs, during 2006 were included. Patients without research authorization or on chronic NIV use for sleep apnea were excluded.
Results:
Out of 1461 Olmsted County adult residents admitted to the ICUs in 2006, 364 patients developed ARF, of which 146 patients were initiated on NIV. The median age in years was 75 (interquartile range, 60&#8211;84), 48% females and 88.7% Caucasians. Eighteen patients (12%) were on Continuous Positive Airway Pressure (CPAP) mode and 128 (88%) were on noninvasive intermittent positive-pressure ventilation (NIPPV) mode. Forty-six (10%) ARF patients were put on NIV for palliative strategy to alleviate dyspnea. Seventy-six ARF patients without treatment limitation were given a trial of NIV and 49 patients succeeded, while 27 had to be intubated. Mortality was similar between the patients initially supported with NIV versus invasive mechanical ventilation (33% vs 22%, P=0.289). In the multivariate analysis, the development of acute respiratory distress syndrome (ARDS) and higher APACHE III scores were associated with the failure of initial NIV treatment.
Conclusions:
Our results have important implications for a future planning of NIV in a suburban US community with high access to critical care services. The higher APACHE III scores and the development of ARDS are associated with the failure of initial NIV treatment.</description>
        <link>http://www.biomedcentral.com/1471-227X/13/6</link>
                <dc:creator>Shihan Wang</dc:creator>
                <dc:creator>Balwinder Singh</dc:creator>
                <dc:creator>Lin Tian</dc:creator>
                <dc:creator>Michelle Biehl</dc:creator>
                <dc:creator>Ivaylo Krastev</dc:creator>
                <dc:creator>Marija Kojicic</dc:creator>
                <dc:creator>Guangxi Li</dc:creator>
                <dc:source>BMC Emergency Medicine 2013, null:6</dc:source>
        <dc:date>2013-04-09T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1471-227X-13-6</dc:identifier>
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                <prism:publicationName>BMC Emergency Medicine</prism:publicationName>
        <prism:issn>1471-227X</prism:issn>
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        <prism:startingPage>6</prism:startingPage>
        <prism:publicationDate>2013-04-09T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.biomedcentral.com/1471-227X/13/5">
        <title>Life threatening intracerebral haemorrhage following saw- scaled viper (Echis carinatus) envenoming-authenticated case report from Sri Lanka</title>
        <description>Background:
Echis carinatus (Saw scaled viper {SSV}) is a venomous snake found in the parts of Middle East and Central Asia. SSV envenoming is characterized by local swelling and coagulopathy. Various bleeding manifestations are commonly seen with SSV envenoming. In contrast to other part of Asia, saw scale viper envenoming has not been reported to cause life threatening haemorrhagic manifestations in Sri Lanka.Case presentationWe report a 19 years old healthy boy who developed massive left temporo-parietal intra cerebral haemorrhage following Echis carinatus (Saw scaled viper) bite in Sri Lanka.
Conclusion:
Although subspecies of SSV in Sri Lanka is regarded as a &#8216;non lethal venomous snake&#8217;, the occurrence of rare potentially fatal complications such as intracerebral haemorrhage should be considered in their management. This case report is intended to bring the awareness of this fatal complication of SSV envenoming in Sri Lanka.</description>
        <link>http://www.biomedcentral.com/1471-227X/13/5</link>
                <dc:creator>Chathuranga Fonseka</dc:creator>
                <dc:creator>Vijayabala Jeevagan</dc:creator>
                <dc:creator>Christeine Gnanathasan</dc:creator>
                <dc:source>BMC Emergency Medicine 2013, null:5</dc:source>
        <dc:date>2013-04-08T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1471-227X-13-5</dc:identifier>
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                <prism:publicationName>BMC Emergency Medicine</prism:publicationName>
        <prism:issn>1471-227X</prism:issn>
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        <prism:startingPage>5</prism:startingPage>
        <prism:publicationDate>2013-04-08T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.biomedcentral.com/1471-227X/13/4">
        <title>Development and pilot implementation of a locally developed Trauma Registry: lessons learnt in a low-income country</title>
        <description>Background:
Trauma registries (TRs) play an integral role in the assessment of trauma care quality. TRs are still uncommon in developing countries owing to awareness and cost. We present a case study of development and pilot implementation of &#8220;Karachi Trauma Registry&#8221; (KITR), using existing medical records at a tertiary-care hospital of Karachi, Pakistan to present results of initial data and describe its process of implementation.
Methods:
KITR is a locally developed, customized, electronic trauma registry based on open source software designed by local software developers in Karachi. Data for KITR was collected from November 2010 to January 2011. All patients presenting to the Emergency Department (ED) of the Aga Khan University Hospital (AKUH) with a diagnosis of injury as defined in ICD-9 CM were included. There was no direct contact with patients or health care providers for data collection. Basic demographics, injury details, event detail, injury severity and outcome were recorded. Data was entered in the KITR and reports were generated.
Results:
Complete data of 542 patients were entered and analysed. The mean age of patients was 27&#8201;years, and 72.5% were males. About 87% of patients had sustained blunt injury. Falls and motor vehicle crashes were the most common mechanisms of injury. Head and face, followed by the extremities, were the most frequently injured anatomical regions. The mean Injury Severity Score (ISS) was 4.99 and there were 8 deaths. The most common missing variables in the medical records were ethnicity, ED notification prior to transfer, and pre-hospital IV fluids. Average time to review each chart was 14.5&#8201;minutes and entry into the electronic registry required 15&#8201;minutes.
Conclusion:
Using existing medical records, we were able to enter data on most variables including mechanism of injuries, burden of severe injuries and quality indicators such as length of stay in ED, injury to arrival delay, as well as generate injury severity and survival probability but missed information such as ethnicity, ED notification. To make the data collection process more effective, we propose provider based data collection or making a standardized data collection tool a part of medical records.</description>
        <link>http://www.biomedcentral.com/1471-227X/13/4</link>
                <dc:creator>Amber Mehmood</dc:creator>
                <dc:creator>Junaid Razzak</dc:creator>
                <dc:creator>Sarah Kabir</dc:creator>
                <dc:creator>Ellen MacKenzie</dc:creator>
                <dc:creator>Adnan Hyder</dc:creator>
                <dc:source>BMC Emergency Medicine 2013, null:4</dc:source>
        <dc:date>2013-03-21T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1471-227X-13-4</dc:identifier>
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                <prism:publicationName>BMC Emergency Medicine</prism:publicationName>
        <prism:issn>1471-227X</prism:issn>
        <prism:volume>${item.volume}</prism:volume>
        <prism:startingPage>4</prism:startingPage>
        <prism:publicationDate>2013-03-21T00:00:00Z</prism:publicationDate>
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                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <item rdf:about="http://www.biomedcentral.com/1471-227X/13/3">
        <title>Advanced accident research system based on a medical and engineering data in the metropolitan area of Florence</title>
        <description>Background:
In the metropolitan area of Florence, 62% of major traumas involve powered two wheeler rider and pillion passengers, 10% cyclists, and 7% pedestrians. The urban and extra-urban areas are the most dangerous for the vulnerable road user. In-depth investigations are needed for assessing detailed information on road accidents. This type of study has been very limited in time frame in Italy, and completely absent in the Tuscan region.Consequently a study called &#8220;In-depth Study of road Accident in FlorencE&#8221; (In-SAFE) has been initiated.
Methods:
A network between the Department of Mechanics and Industrial Technologies (University of Florence) and the Intensive Care Unit of the Emergency Department (Careggi Teaching Hospital, Florence) was created with the aim of collecting information about the road accidents. The data collected includes: on-scene data, data coming from examination of the vehicles, kinematics and dynamic crash data, injuries, treatment, and injury mechanisms. Each injury is codified thorough the AIS score, localized by a three-dimensional human body model based on computer tomography slices, and the main scores are calculated. We then associate each injury with its cause and crash technical parameters. Finally, all the information is collected in the In-SAFE database.
Results:
Patient mean age at the time of the accident was 34.6&#160;years, and 80% were males. The ISS mean is 24.2 (SD 8.7) and the NISS mean is 33.6 (SD 10.5). The main road accident configurations are the &#8220;car-to-PTW&#8221; (25%) and &#8220;pedestrian run over&#8221; (17,9%). For the former, the main collision configuration is &#8220;head-on crash&#8221; (57%). Cyclists and PTW riders-and-pillions-passengers suffer serious injuries (AIS3+) mainly to the head and the thorax. The head (56.4%) and the lower extremities (12.7%) are the most frequently injured pedestrian body regions.
Conclusions:
The aim of the project is to create an in-depth road accident study with special focus on the correlation between technical parameters and injuries. An in-depth investigation team was setup and is currently active in the metropolitan area of Florence.Twenty-eight serious road accidents involving twenty-nine ICU patients are studied. PTW users, cyclist and pedestrians are the most frequently involved in metropolitan accidents.</description>
        <link>http://www.biomedcentral.com/1471-227X/13/3</link>
                <dc:creator>Simone Piantini</dc:creator>
                <dc:creator>David Grassi</dc:creator>
                <dc:creator>Marco Mangini</dc:creator>
                <dc:creator>Marco Pierini</dc:creator>
                <dc:creator>Giovanni Zagli</dc:creator>
                <dc:creator>Rosario Spina</dc:creator>
                <dc:creator>Adriano Peris</dc:creator>
                <dc:source>BMC Emergency Medicine 2013, null:3</dc:source>
        <dc:date>2013-03-14T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1471-227X-13-3</dc:identifier>
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                <prism:publicationName>BMC Emergency Medicine</prism:publicationName>
        <prism:issn>1471-227X</prism:issn>
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        <prism:startingPage>3</prism:startingPage>
        <prism:publicationDate>2013-03-14T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.biomedcentral.com/1471-227X/13/2">
        <title>Risk and clinical-outcome indicators of delirium in an emergency department intermediate care unit (EDIMCU): an observational prospective study</title>
        <description>Background:
Identification of delirium in emergency departments (ED) is often underestimated; within EDs, studies on delirium assessment and relation with patient outcome in Intermediate Care Units (IMCU) appear missing in European hospital settings. Here we aimed to determine delirium prevalence in an EDIMCU (Hospital de Braga, Braga, Portugal) and assessed routine biochemical parameters that might be delirium indicators.
Methods:
The study was prospective and observational. Sedation level was assessed via the Richmond Agitation-Sedation Scale and delirium status by the Confusion Assessment Method for the ICU. Information collected included age and gender, admission type, Charlson Comorbidity Index combined condition score (Charlson score), systemic inflammatory response syndrome criteria (SIRS), biochemical parameters (blood concentration of urea nitrogen, creatinine, hemoglobin, sodium and potassium, arterial blood gases, and other parameters as needed depending on clinical diagnosis) and EDIMCU length of stay (LOS). Statistical analyses were performed as appropriate to determine if baseline features differed between the &#8216;Delirium&#8217; and &#8216;No Delirium&#8217; groups. Multivariate logistic regression was performed to assess the effect of delirium on the 1-month outcome.
Results:
Inclusion and exclusion criteria were met in 283 patients; 238 were evaluated at 1-month for outcome follow-up after EDIMCU discharge (&#8220;good&#8221; recovery without complications requiring hospitalization or institutionalization; &#8220;poor&#8221; institutionalization in permanent care-units/assisted-living or death). Delirium was diagnosed in 20.1% patients and was significantly associated with longer EDIMCU LOS. At admission, Delirium patients were significantly older and had significantly higher blood urea, creatinine and osmolarity levels and significantly lower hemoglobin levels, when compared with No Delirium patients. Delirium was an independent predictor of increased EDIMCU LOS (odds ratio 3.65, 95% CI 1.97-6.75) and poor outcome at 1-month after discharge (odds ratio 3.51, CI 1.84-6.70), adjusted for age, gender, admission type, presence of SIRS criteria, Charlson score and osmolarity at admission.
Conclusions:
In an EDIMCU setting, delirium was associated with longer LOS and poor outcome at1-month post-discharge. Altogether, findings support the need for delirium screening and management in emergency settings.</description>
        <link>http://www.biomedcentral.com/1471-227X/13/2</link>
                <dc:creator>José Mariz</dc:creator>
                <dc:creator>Nadine Santos</dc:creator>
                <dc:creator>Hugo Afonso</dc:creator>
                <dc:creator>Pedro Rodrigues</dc:creator>
                <dc:creator>António Faria</dc:creator>
                <dc:creator>Nuno Sousa</dc:creator>
                <dc:creator>Jorge Teixeira</dc:creator>
                <dc:source>BMC Emergency Medicine 2013, null:2</dc:source>
        <dc:date>2013-01-29T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1471-227X-13-2</dc:identifier>
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                <prism:publicationName>BMC Emergency Medicine</prism:publicationName>
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        <prism:startingPage>2</prism:startingPage>
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        <item rdf:about="http://www.biomedcentral.com/1471-227X/13/1">
        <title>Missing the boat: odds for the patients who leave ED without being seen</title>
        <description>Background:
A patient left without being seen is a well-recognized indicator of Emergency Department overcrowding. The aim of this study was to define the characteristics of LWBS patients, their rates and associated factors from a tertiary care hospital of Pakistan.
Methods:
A retrospective patient record review was undertaken. All patients presenting to the Aga Khan University Hospital, Karachi, between April and December of the year 2010, were included in the study. Information was collected on age, sex, presenting complaints, ED capacity, month, time, shift, day of the week, and waiting times in the ED. A basic descriptive analysis was made and the rates of LWBS patients were determined among the patient subgroups. Logistic regression analysis was used to assess the risk factors associated with a patient not being seen in the ED.
Results:
A total of 38,762 patients visited ED during the study period. Among them 5,086 (13%) patients left without being seen. Percentage of leaving was highest in the night shift (20%). The percentage was twice as high when the ED was on diversion (19.8%) compared to regular periods of operation (9.8%). Mean waiting time before leaving the ED in pediatric patients was 154 minutes while for adults it was 171 minutes. More than 32% of patients had waited for more than 180 minutes before they left without being seen, compared to the patients who were seen in ED. Important predictors for LWBS included; Triage category P4 i.e. walk &#8211;in-patients had an OR of 13.62(8.72-21.3), Diversion status, OR 1.49(1.26-1.76), night shift , OR 2.44(1.95-3.05) and Pediatric age, OR 0.57(0.48-0.66).
Conclusions:
Our study elucidates the LWBS population characteristics and identifies the risk factors for this phenomenon. Targeted interventions should be planned and implemented to decrease the waiting time and alternate services should be provided for high-risk patients (for LWBS) to minimize their number.</description>
        <link>http://www.biomedcentral.com/1471-227X/13/1</link>
                <dc:creator>Jabeen Fayyaz</dc:creator>
                <dc:creator>Munawar Khursheed</dc:creator>
                <dc:creator>Mohammed Umer Mir</dc:creator>
                <dc:creator>Amber Mehmood</dc:creator>
                <dc:source>BMC Emergency Medicine 2013, null:1</dc:source>
        <dc:date>2013-01-16T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1471-227X-13-1</dc:identifier>
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                <prism:publicationName>BMC Emergency Medicine</prism:publicationName>
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        <prism:startingPage>1</prism:startingPage>
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        <item rdf:about="http://www.biomedcentral.com/1471-227X/12/19">
        <title>Development and evaluation of a novel, real time mobile telesonography system in management of patients with abdominal trauma: study protocol</title>
        <description>Background:
Despite the use of e-FAST in management of patients with abdominal trauma, its utility in prehospital setting is not widely adopted. The goal of this study is to develop a novel portable telesonography (TS) system and evaluate the comparability of the quality of images obtained via this system among healthy volunteers who undergo e-FAST abdominal examination in a moving ambulance and at the ED. We hypothesize that: (1) real-time ultrasound images of acute trauma patients in the pre-hospital setting can be obtained and transmitted to the ED via the novel TS system; and (2) Ultrasound images transmitted to the hospital from the real-time TS system will be comparable in quality to those obtained in the ED.
Methods:
Study participants are three healthy volunteers (one each with normal, overweight and obese BMI category). The ultrasound images will be obtained by two ultrasound-trained physicians The TS is a portable sonogram (by Sonosite) interfaced with a portable broadcast unit (by Live-U). Two UTPs will conduct e-FAST examinations on healthy volunteers in moving ambulances and transmit the images via cellular network to the hospital server, where they are stored. Upon arrival in the ED, the same UTPs will obtain another set of images from the volunteers, which are then compared to those obtained in the moving ambulances by another set of blinded UTPs (evaluators) using a validated image quality scale, the Questionnaire for User Interaction Satisfaction (QUIS).DiscussionFindings from this study will provide needed data on the validity of the novel TS in transmitting live images from moving ambulances to images obtained in the ED thus providing opportunity to facilitate medical care of a patient located in a remote or austere setting.</description>
        <link>http://www.biomedcentral.com/1471-227X/12/19</link>
                <dc:creator>Chinwe Ogedegbe</dc:creator>
                <dc:creator>Herman Morchel</dc:creator>
                <dc:creator>Vikki Hazelwood</dc:creator>
                <dc:creator>William Chaplin</dc:creator>
                <dc:creator>Joseph Feldman</dc:creator>
                <dc:source>BMC Emergency Medicine 2012, null:19</dc:source>
        <dc:date>2012-12-18T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1471-227X-12-19</dc:identifier>
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                <prism:publicationName>BMC Emergency Medicine</prism:publicationName>
        <prism:issn>1471-227X</prism:issn>
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        <prism:startingPage>19</prism:startingPage>
        <prism:publicationDate>2012-12-18T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.biomedcentral.com/1471-227X/12/18">
        <title>Novel electronic refreshers for cardiopulmonary resuscitation: a randomized controlled trial</title>
        <description>Background:
Currently the American Red Cross requires that individuals renew their cardiopulmonary resuscitation (CPR) certification annually; this often requires a 4- to 8-hour refresher course. Those trained in CPR often show a decrease in essential knowledge and skills within just a few months after training. New electronic means of communication have expanded the possibilities for delivering CPR refreshers to members of the general public who receive CPR training. The study&#8217;s purpose was to determine the efficacy of three novel CPR refreshers - online website, e-mail and text messaging &#8211; for improving three outcomes of CPR training - skill retention, confidence for using CPR and intention to use CPR. These three refreshers may be considered &#8220;novel&#8221; in that they are not typically used to refresh CPR knowledge and skills.
Methods:
The study conducted two randomized clinical trials of the novel CPR refreshers. A mailed brochure was a traditional, passive refresher format and served as the control condition. In Trial 1, the refreshers were delivered in a single episode at 6 months after initial CPR training. In Trial 2, the refreshers were delivered twice, at 6 and 9 months after initial CPR training, to test the effect of a repeated delivery. Outcomes for the three novel refreshers vs. the mailed brochure were determined at 12 months after initial CPR training.
Results:
Assignment to any of three novel refreshers did not improve outcomes of CPR training one year later in comparison with receiving a mailed brochure. Comparing outcomes for subjects who actually reviewed some of the novel refreshers vs. those who did not indicated a significant positive effect for one outcome, confidence for performing CPR. The website refresher was associated with increased behavioral intent to perform CPR. Stated satisfaction with the refreshers was relatively high. The number of episodes of refreshers (one vs. two) did not have a significant effect on any outcomes.
Conclusions:
There was no consistent evidence for the superiority of novel refreshers as compared with a traditional mailed brochure, but the low degree of actual exposure to the materials does not allow a definitive conclusion. An online web-based approach seems to have the most promise for future research on electronic CPR refreshers.</description>
        <link>http://www.biomedcentral.com/1471-227X/12/18</link>
                <dc:creator>Stephen Magura</dc:creator>
                <dc:creator>Michael Miller</dc:creator>
                <dc:creator>Timothy Michael</dc:creator>
                <dc:creator>Robert Bensley</dc:creator>
                <dc:creator>Jason Burkhardt</dc:creator>
                <dc:creator>Anne Puente</dc:creator>
                <dc:creator>Carolyn Sullins</dc:creator>
                <dc:source>BMC Emergency Medicine 2012, null:18</dc:source>
        <dc:date>2012-11-21T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1471-227X-12-18</dc:identifier>
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                <prism:publicationName>BMC Emergency Medicine</prism:publicationName>
        <prism:issn>1471-227X</prism:issn>
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        <prism:startingPage>18</prism:startingPage>
        <prism:publicationDate>2012-11-21T00:00:00Z</prism:publicationDate>
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                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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