1
and the actual outcome for the same subject. The closer the score is to 0, the better the predictions. Results: The study enrolled 497 patients between June 9, 2010 and February 28, 2013. Of these patients, 377 (76%) had no 30-day adverse events, 39 (8%) had an AF- related ED return visit, 32 (6%) were hospitalized for AF-related problem, 13 (3%) patients suffered strokes, and 4 (<1%) had an AF-related death. The ORs (95% CI) for the decision aid in the original derivation cohort and in this validation cohort are reported in the Table. The c-statistic was 0.66 (95% CI, 0.6 to 0.71), which is similar to the c-statistic of 0.67 (95% CI, 0.63 to 0.71) obtained from the derivation cohort. The mean Brier scores for the decision aids performance at predicting the occurrence of a 30-day adverse event was 0.06. Conclusion: We found that our previously derived decision aid performed well in a prospective cohort of ED patients with symptomatic AF. This validation study supports that increased patient age, inadequate 2-hour ventricular rate control, impaired respiratory status, and smoking history increase AF patients risk for 30-day adverse events. Table. Decision Aid For 30-Day Adverse Events In ED Patients With Atrial Fibrillation Predictor Derivation Cohort (n[832) Odds Ratio 95% Condence Intervals Validation Cohort (n[497) Odds Ratio 95% Condence Intervals Smoker 2.35 (1.47, 3.76) 2.17 (1.17, 4.04) Inadequate 2-Hour ED Ventricular Rate Control 1.58 (1.13, 2.21) 1.85 (1.19, 2.90) Complaint Of Dyspnea 1.57 (1.12, 2.20) 1.51 (0.95, 2.40) Home Beta-Blocker Use 1.44 (1.02, 2.39) 1.50 (0.94, 2.40) Age (1 year increment) 1.02 (1.00, 1.04) 1.02 (1.00, 1.04) Female 1.11 (0.79, 1.56) 0.95 (0.60, 1.49) Home Use of Diuretic 1.00 (0.69, 1.44) 1.11 (0.67, 1.84) Heart Failure 1.35 (0.92, 1.98) 1.08 (0.64, 1.82) Peripheral Edema 1.28 (0.89, 1.85) 1.06 (0.67, 1.69) COPD 1.08 (0.69, 1.69) 1.08 (0.60, 1.93) Hypertension 1.21 (0.82, 1.79) 0.91 (0.52, 1.56) Palpitations in the ED 0.90 (0.63, 1.30) 1.42 (0.68, 2.99) COPD, Chronic Obstructive Pulmonary Disease. 13 Ketamine Use in a Resource-Limited Setting: Continued Safety in a Maturing African Non-Physician Clinician System Bisanzo M, Brandt R, Kisoke T, Kyomugisha F, Arthur AO, Thomas SH/UMASS/GECC, Boston, MA; Global Emergency Care Collaborative, Boston, MA; Karoli Lwanga Hospital, Rukungiri, Uganda; University of Oklahoma, Tulsa, OK Study Objective: We have previously reported a series of ketamine administrations for procedural sedation and analgesia (PSA) by non-physician clinicians in a resource- limited hospital in rural Uganda. Ketamine continues as the primary PSA agent, and the emergency care practitioner training program continues to evolve. Inaugural class graduates of the program are now training and educating others in the use of ketamine PSA (Train the Trainer Model). Re-evaluation of the safety and efcacy of ketamine is required to ensure there was no degradation in patient safety with transition of these training responsibilities to non-physicians. Methods: This was a prospective observational study conducted in the emergency department of a rural district hospital in Uganda. The study compared patients from the time frame of the initial ketamine study, 11/2009 - 3/2010, with those given ketamine in the latter time frame, 3/2013 - 3/2014. Data collected included demographics, past medical history, and current medical issues. Subjects were monitored for vital signs and complications. Patients (or attendants/parents) were asked about amnesia, procedural pain, and whether they would want ketamine for a future procedure. Descriptive statistics included mean standard deviation (SD) for normal data and median with interquartile range (IQR) for non-normal data. Categorical data was assessed with Fishers exact testing and continuous variables with nonparametric Kruskal-Wallis testing. Binomial exact 95% condence intervals (CIs) were calculated for proportions. Univariate analysis was conducted with relative risk reported as odds ratio (OR). Multivariate logistic regression was used to adjust for covariates and potential confounders. All analyses were conducted with STATA 13MP (StataCorp, College Station, TX); signicance was dened as P<.05. Results: The study encompassed 191 patients from the earlier time frame and 162 from the latter. PSA was provided for procedures ranging from wound care to fasciotomy, urologic procedures, fracture reduction, burn care, and incision/drainage of abscesses. Total procedural completion success rate for ketamine PSA was 99%. The overall median age was 12 years (IQR 3-26), with the latter group being signicantly younger, (7 versus 17, P¼.005). There were more female patients in the latter timeframe than in the earlier (58% versus 43%, P¼.005) Patients in the latter timeframe were less likely (P<.001) to have upper respiratory infection (URI) concurrent with PSA (2% versus 16%). New hypoxemia events were similar during the latter timeframe compared to the initial timeframe (OR .26, 95% CI .15-.43). There were no deaths or major sequelae from ketamine PSA. There was no statistically signicant difference between the time frames regarding amnesia (92% versus 86%), procedural pain (5% versus 8%), or wanting ketamine for a future procedure (98% versus 96%). Vomiting (5% versus 0.6%) and emergence reactions (4% versus 0.6%) occurred less frequently in the latter timeframe. Conclusions: After introduction of a non-physician clinician-directed ketamine PSA program, initial trainees were able to successfully train additional providers with continued patient safety and no loss of efcacy. In this resource-limited setting, non- physician clinician administration of ketamine PSA is highly safe and effective for a variety of procedure types. 14 Computed Tomography for Pulmonary Embolism: A Prospective Evaluation of Utilization in the Emergency Department Myong AS, Baliga SB, Klausner HA, Oddo M/Henry Ford Hospital, Detroit, MI Study Objectives: Patients are routinely evaluated for pulmonary embolism in emergency departments across the country. Clinical decision rules such as Wellscriteria and the Pulmonary Embolism Rule Out Criteria (PERC) have been developed to aid an emergency physician in determining who needs further evaluation for pulmonary embolism. Despite the presence of these clinical decision rules, there is little data on how clinicians decide who needs evaluation for pulmonary embolism. The objective of the study is to determine what clinical factors emergency physicians use to order computed tomography (CT) scans to evaluate for pulmonary embolism and which factors are most associated with diagnosing a pulmonary embolism. Methods: Clinicians at an inner-city academic emergency department who ordered a CT scan on a patient to evaluate for a pulmonary embolism were asked to complete a form indicating which historical and clinical factors were used to determine the need for testing and the clinical suspicion for diagnosing a pulmonary embolism. Patients above the age of 18 were enrolled prospectively from February 2012 to March 2013. The study obtained IRB approval. Over 20 historical and physical exam ndings, 10 comorbidities, and clinical decision rules such as Wellsscore and the PERC rule were analyzed to determine if there was a correlation with ordering a CT and diagnosing a pulmonary embolism. SAS version 9.2 was used to perform data analysis. Chi-squared test was use for univariate analysis, while multivariable logistic regression was used for multivariate analysis. Results: A total of 353 patients were included in the study with 22 patients (6.2%) having a CT scan positive for a pulmonary embolism. Over 84% of the patients (300) had four or more indications for having a CT scan ordered, with the most common reasons being dyspnea (70.9%), chest pain (59.3%), and tachycardia (38.7%). Clinicians had a low suspicion for pulmonary embolism on 150 patients (42.5%) and moderate to high suspicion on 203 patients (57.5%). Univariate analysis shows only history of deep venous thrombosis (OR 4.59:1, P¼0.004), history of cancer (OR 2.97:1, P¼0.025), and an elevated Wellsscore (OR 1.35:1, P¼0.002) were statistically signicant in predicting a pulmonary embolism. In multivariate analysis, only history of DVT (OR 4.00:1, P¼0.023) and history of cancer (OR 2.91:1, P¼0.048) were statistically signicant in diagnosing a pulmonary embolism. Conclusion: Emergency department clinicians often cite multiple factors when ordering a CT scan to evaluate for a pulmonary embolism. Only history of DVT and history of cancer were statistically signicant in identifying patients with pulmonary embolism. No other clinical factors can accurately predict the presence or absence of pulmonary embolism. S6 Annals of Emergency Medicine Volume 64, no. 4s : October 2014 Research Forum Abstracts

13 Ketamine Use in a Resource-Limited Setting: Continued Safety in a Maturing African Non-Physician Clinician System

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Research Forum Abstracts

and the actual outcome for the same subject. The closer the score is to 0, the betterthe predictions.

Results: The study enrolled 497 patients between June 9, 2010 and February 28,2013. Of these patients, 377 (76%) had no 30-day adverse events, 39 (8%) had an AF-related ED return visit, 32 (6%) were hospitalized for AF-related problem, 13 (3%)patients suffered strokes, and 4 (<1%) had an AF-related death. The ORs (95% CI)for the decision aid in the original derivation cohort and in this validation cohort arereported in the Table. The c-statistic was 0.66 (95% CI, 0.6 to 0.71), which is similarto the c-statistic of 0.67 (95% CI, 0.63 to 0.71) obtained from the derivation cohort.The mean Brier scores for the decision aid’s performance at predicting the occurrenceof a 30-day adverse event was 0.06.

Conclusion: We found that our previously derived decision aid performed well in aprospective cohort of ED patients with symptomatic AF. This validation studysupports that increased patient age, inadequate 2-hour ventricular rate control,impaired respiratory status, and smoking history increase AF patient’s risk for 30-dayadverse events.

Table. Decision Aid For 30-Day Adverse Events In ED Patients With AtrialFibrillation

Derivation Validation

Predictor

S6 Annals of Emergen

Cohort(n[832)Odds Ratio

cy Medicine

95%ConfidenceIntervals

Cohort(n[497)Odds Ratio

95%ConfidenceIntervals

Smoker

2.35 (1.47, 3.76) 2.17 (1.17, 4.04) Inadequate 2-Hour ED

Ventricular Rate Control

1.58 (1.13, 2.21) 1.85 (1.19, 2.90)

Complaint Of Dyspnea

1.57 (1.12, 2.20) 1.51 (0.95, 2.40) Home Beta-Blocker Use 1.44 (1.02, 2.39) 1.50 (0.94, 2.40) Age (1 year increment) 1.02 (1.00, 1.04) 1.02 (1.00, 1.04) Female 1.11 (0.79, 1.56) 0.95 (0.60, 1.49) Home Use of Diuretic 1.00 (0.69, 1.44) 1.11 (0.67, 1.84) Heart Failure 1.35 (0.92, 1.98) 1.08 (0.64, 1.82) Peripheral Edema 1.28 (0.89, 1.85) 1.06 (0.67, 1.69) COPD 1.08 (0.69, 1.69) 1.08 (0.60, 1.93) Hypertension 1.21 (0.82, 1.79) 0.91 (0.52, 1.56) Palpitations in the ED 0.90 (0.63, 1.30) 1.42 (0.68, 2.99)

COPD, Chronic Obstructive Pulmonary Disease.

Ketamine Use in a Resource-Limited Setting: Continued

13 Safety in a Maturing African Non-Physician Clinician SystemBisanzo M, Brandt R, Kisoke T, Kyomugisha F, Arthur AO, Thomas SH/UMASS/GECC,Boston, MA; Global Emergency Care Collaborative, Boston, MA; Karoli LwangaHospital, Rukungiri, Uganda; University of Oklahoma, Tulsa, OK

Study Objective: We have previously reported a series of ketamine administrationsfor procedural sedation and analgesia (PSA) by non-physician clinicians in a resource-limited hospital in rural Uganda. Ketamine continues as the primary PSA agent,and the emergency care practitioner training program continues to evolve. Inauguralclass graduates of the program are now training and educating others in the use ofketamine PSA (Train the Trainer Model). Re-evaluation of the safety and efficacy ofketamine is required to ensure there was no degradation in patient safety withtransition of these training responsibilities to non-physicians.

Methods: This was a prospective observational study conducted in the emergencydepartment of a rural district hospital in Uganda. The study compared patients fromthe time frame of the initial ketamine study, 11/2009 - 3/2010, with those givenketamine in the latter time frame, 3/2013 - 3/2014.

Data collected included demographics, past medical history, and currentmedical issues. Subjects were monitored for vital signs and complications. Patients(or attendants/parents) were asked about amnesia, procedural pain, and whether theywould want ketamine for a future procedure. Descriptive statistics included mean �standard deviation (SD) for normal data and median with interquartile range (IQR) fornon-normal data. Categorical data was assessed with Fisher’s exact testing andcontinuous variables with nonparametric Kruskal-Wallis testing. Binomial exact 95%confidence intervals (CIs) were calculated for proportions. Univariate analysis was

conducted with relative risk reported as odds ratio (OR). Multivariate logisticregression was used to adjust for covariates and potential confounders. All analyses wereconducted with STATA 13MP (StataCorp, College Station, TX); significance wasdefined as P<.05.

Results: The study encompassed 191 patients from the earlier time frame and 162from the latter. PSA was provided for procedures ranging from wound care tofasciotomy, urologic procedures, fracture reduction, burn care, and incision/drainage ofabscesses. Total procedural completion success rate for ketamine PSA was 99%. Theoverall median age was 12 years (IQR 3-26), with the latter group being significantlyyounger, (7 versus 17, P¼.005). There were more female patients in the lattertimeframe than in the earlier (58% versus 43%, P¼.005) Patients in the lattertimeframe were less likely (P<.001) to have upper respiratory infection (URI)concurrent with PSA (2% versus 16%). New hypoxemia events were similar during thelatter timeframe compared to the initial timeframe (OR .26, 95% CI .15-.43). Therewere no deaths or major sequelae from ketamine PSA. There was no statisticallysignificant difference between the time frames regarding amnesia (92% versus 86%),procedural pain (5% versus 8%), or wanting ketamine for a future procedure (98%versus 96%). Vomiting (5% versus 0.6%) and emergence reactions (4% versus 0.6%)occurred less frequently in the latter timeframe.

Conclusions: After introduction of a non-physician clinician-directed ketaminePSA program, initial trainees were able to successfully train additional providers withcontinued patient safety and no loss of efficacy. In this resource-limited setting, non-physician clinician administration of ketamine PSA is highly safe and effective for avariety of procedure types.

Computed Tomography for Pulmonary Embolism: A

14 Prospective Evaluation of Utilization in the EmergencyDepartment

Myong AS, Baliga SB, Klausner HA, Oddo M/Henry Ford Hospital, Detroit, MI

Study Objectives: Patients are routinely evaluated for pulmonary embolism inemergency departments across the country. Clinical decision rules such as Wells’criteria and the Pulmonary Embolism Rule Out Criteria (PERC) have beendeveloped to aid an emergency physician in determining who needs further evaluationfor pulmonary embolism. Despite the presence of these clinical decision rules,there is little data on how clinicians decide who needs evaluation for pulmonaryembolism. The objective of the study is to determine what clinical factors emergencyphysicians use to order computed tomography (CT) scans to evaluate for pulmonaryembolism and which factors are most associated with diagnosing a pulmonaryembolism.

Methods: Clinicians at an inner-city academic emergency department who ordereda CT scan on a patient to evaluate for a pulmonary embolism were asked to complete aform indicating which historical and clinical factors were used to determine the needfor testing and the clinical suspicion for diagnosing a pulmonary embolism. Patientsabove the age of 18 were enrolled prospectively from February 2012 to March 2013.The study obtained IRB approval. Over 20 historical and physical exam findings, 10comorbidities, and clinical decision rules such as Wells’ score and the PERC rule wereanalyzed to determine if there was a correlation with ordering a CT and diagnosing apulmonary embolism. SAS version 9.2 was used to perform data analysis. Chi-squaredtest was use for univariate analysis, while multivariable logistic regression was used formultivariate analysis.

Results: A total of 353 patients were included in the study with 22 patients(6.2%) having a CT scan positive for a pulmonary embolism. Over 84% of thepatients (300) had four or more indications for having a CT scan ordered, with themost common reasons being dyspnea (70.9%), chest pain (59.3%), and tachycardia(38.7%). Clinicians had a low suspicion for pulmonary embolism on 150 patients(42.5%) and moderate to high suspicion on 203 patients (57.5%). Univariateanalysis shows only history of deep venous thrombosis (OR 4.59:1, P¼0.004),history of cancer (OR 2.97:1, P¼0.025), and an elevated Wells’ score (OR 1.35:1,P¼0.002) were statistically significant in predicting a pulmonary embolism. Inmultivariate analysis, only history of DVT (OR 4.00:1, P¼0.023) and history ofcancer (OR 2.91:1, P¼0.048) were statistically significant in diagnosing apulmonary embolism.

Conclusion: Emergency department clinicians often cite multiple factors whenordering a CT scan to evaluate for a pulmonary embolism. Only history of DVT andhistory of cancer were statistically significant in identifying patients with pulmonaryembolism. No other clinical factors can accurately predict the presence or absence ofpulmonary embolism.

Volume 64, no. 4s : October 2014