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There was no difference between medical or surgical patients, 44.2% versus 53.6%, respectively (odds ratio 0.69, 95% con- fidence interval 0.38-1.24). The most common risk factors were immobilization (70.6%), infection (44.3%), cancer (27.5%), and obesity (23.3%). There were patients who re- ceived substandard care, as they had high risk of VTE. Those who had three or more risk factors, and patients with cancer, received prophylaxis in 25% and 18% of cases, respectively. DISCUSSION (CONCLUSION): In agreement with previ- ous published studies, we found low adherence to best prac- tices. Actions have been carried out on patients with cancer and three or more risk factors. The use of an electronic template integrated in the EHR has been crucial for quality improve- ment. TARGET AUDIENCE(S): 1. Evidence synthesizer, developer of systematic reviews or meta-analyses 2. Guideline implementer 3. Quality improvement manager/facilitator 4. Medical educator 5. Health care policy analyst/policy-maker P3Existing clinical assessment tools and diagnostic strategies for pulmonary embolism Natalia Lekerika-Royo, MD (Presenter) (Osakidetza, Berango, Bizkaia, Spain); Eunate Arana-Arri, PhD (Osakidetza, Barakaldo, Spain); Lorena Lo ´ pez-Rolda ´ n, MD (Osakidetza, Barakaldo, Spain); Larraitz Garcı´a Echeberria, MD (Osakidetza, Barakaldo, Spain); Ana Garcı´a Montero, MD (Osakidetza, Barakaldo, Spain); Maider Garmendia Zallo, MD (Osakidetza, Barakaldo, Spain); Ainhoa Go ´ mez Bonilla, MD (Osakidetza, Barakaldo, Spain); Valentin Cabriada Nun ˜ o, MD (Osakidetza, 48903, Spain) PRIMARY TRACK: Evidence generation and synthesis SECONDARY TRACK: Evidence appraisal BACKGROUND (INTRODUCTION): Acute pulmonary embolism (PE) is of interest to physicians of almost all disci- plines, as it is encountered across the entire spectrum of clinical medicine. It is estimated that as many as 200,000 patients die annually of PE in the European Union, with similar numbers reported in the USA. In the past, management of acute PE has been characterized by a high degree of complexity and a disappointing lack of efficacy and efficiency. LEARNING OBJECTIVES (TRAINING GOALS): 1. To summarize the evidence regarding the existing clin- ical probability assessment tools. 2. To analyze the diagnostic strategies and algorithms. METHODS: We performed a comprehensive review (over- view), including experimental studies, protocols, guidelines, recommendations, and standards for clinical prognostic models and tools and diagnostic algorithms. The databases consulted were MEDLINE, EMBASE, Cochrane, CRD, and NGC; and the websites of the following societies: ESC, ACC, ACEP, BTS, ACP, ATS, CTS and STS. The limits used were: human, subjects, 2000-2009 (December). The studies included were RCTs, meta-analysis and systematic reviews (SR), and clinical guidelines (CPG). RESULTS: Thirty-nine documents out of 86 met inclusion criteria. The largest numbers of them included no systematic reviews, seven CPGs, nine RCTs, and eight SRs. There was great variability in the description of the risk factors associated with PE. When describing the clinical probability assessment tools, 30 describe the Wells score, 16 describe the Geneva score, and 8 describe others (Minniati, Kline, PIOPED, Perrier, and Wicki). One study even described its own score. All algorithms began by a clinical rule, but only eight of them specify the score to use. DISCUSSION (CONCLUSION): We have observed a high variability while using different algorithms and by the use of different imaging studies. Those algorithms are not justified by context differences. TARGET AUDIENCE(S): 1. Clinical researcher 2. Guideline developer 3. Guideline implementer 4. Developer of guideline-based products 5. Quality improvement manager/facilitator 6. Health care policy analyst/policy-maker 7. Health insurance payers and purchasers 8. Medical providers and executives 9. Consumers and patients representatives P4“Best Available” evidence does not mean “best” studies are available Danette Stanko-Lopp, MPH (Presenter) (Cincinnati Children’s Hospital Medical Center, Cincinnati, Ohio) PRIMARY TRACK: Evidence generation and synthesis SECONDARY TRACK: Evidence appraisal BACKGROUND (INTRODUCTION): To address evi- dence appraisal related to a variety of clinical questions in an interprofessional atmosphere and to provide simple, transpar- ent evidence appraisal forms, thus improving access to evi- dence evaluation for point-of-care clinicians. LEARNING OBJECTIVES (TRAINING GOALS): 1. Understand evidence appraisal of study for quality. 2. Identify the domain of a clinical question and study designs appropriate for each domain. 3. Determine a quality level/grade based on three factors of domain, study design, and quality appraisal. METHODS: Evidence appraisal forms were developed for multiple study designs specific to each domain. Each appraisal form includes questions about the validity, reliability, and applicability of a study. Additionally, an appraisal form was created to appraise each study design available or possible for a given domain. The multiple study designs by clinical ques- tion domain are captured in a three-dimensional matrix with the resulting quality level from the appraisal. 80 Otolaryngology–Head and Neck Surgery, Vol 143, No 1S1, July 2010

P3– Existing clinical assessment tools and diagnostic strategies for pulmonary embolism

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There was no difference between medical or surgical patients,44.2% versus 53.6%, respectively (odds ratio 0.69, 95% con-fidence interval 0.38-1.24). The most common risk factorswere immobilization (70.6%), infection (44.3%), cancer(27.5%), and obesity (23.3%). There were patients who re-ceived substandard care, as they had high risk of VTE. Thosewho had three or more risk factors, and patients with cancer,received prophylaxis in 25% and 18% of cases, respectively.DISCUSSION (CONCLUSION): In agreement with previ-ous published studies, we found low adherence to best prac-tices. Actions have been carried out on patients with cancer andthree or more risk factors. The use of an electronic templateintegrated in the EHR has been crucial for quality improve-ment.TARGET AUDIENCE(S):

1. Evidence synthesizer, developer of systematic reviews ormeta-analyses

2. Guideline implementer3. Quality improvement manager/facilitator4. Medical educator5. Health care policy analyst/policy-maker

P3– Existing clinical assessment tools and

diagnostic strategies for pulmonary embolism

Natalia Lekerika-Royo, MD (Presenter) (Osakidetza,Berango, Bizkaia, Spain); Eunate Arana-Arri, PhD(Osakidetza, Barakaldo, Spain);Lorena Lopez-Roldan, MD (Osakidetza, Barakaldo,Spain); Larraitz Garcıa Echeberria, MD (Osakidetza,Barakaldo, Spain); Ana Garcıa Montero, MD(Osakidetza, Barakaldo, Spain);Maider Garmendia Zallo, MD (Osakidetza,Barakaldo, Spain); Ainhoa Gomez Bonilla, MD(Osakidetza, Barakaldo, Spain);Valentin Cabriada Nuno, MD (Osakidetza, 48903,Spain)

PRIMARY TRACK: Evidence generation and synthesisSECONDARY TRACK: Evidence appraisalBACKGROUND (INTRODUCTION): Acute pulmonaryembolism (PE) is of interest to physicians of almost all disci-plines, as it is encountered across the entire spectrum of clinicalmedicine. It is estimated that as many as 200,000 patients dieannually of PE in the European Union, with similar numbersreported in the USA. In the past, management of acute PE hasbeen characterized by a high degree of complexity and adisappointing lack of efficacy and efficiency.LEARNING OBJECTIVES (TRAINING GOALS):

1. To summarize the evidence regarding the existing clin-ical probability assessment tools.

2. To analyze the diagnostic strategies and algorithms.METHODS: We performed a comprehensive review (over-view), including experimental studies, protocols, guidelines,recommendations, and standards for clinical prognostic modelsand tools and diagnostic algorithms. The databases consultedwere MEDLINE, EMBASE, Cochrane, CRD, and NGC; and

the websites of the following societies: ESC, ACC, ACEP,BTS, ACP, ATS, CTS and STS. The limits used were: human,subjects, 2000-2009 (December). The studies included wereRCTs, meta-analysis and systematic reviews (SR), and clinicalguidelines (CPG).RESULTS: Thirty-nine documents out of 86 met inclusioncriteria. The largest numbers of them included no systematicreviews, seven CPGs, nine RCTs, and eight SRs. There wasgreat variability in the description of the risk factors associatedwith PE. When describing the clinical probability assessmenttools, 30 describe the Wells score, 16 describe the Genevascore, and 8 describe others (Minniati, Kline, PIOPED, Perrier,and Wicki). One study even described its own score. Allalgorithms began by a clinical rule, but only eight of themspecify the score to use.DISCUSSION (CONCLUSION): We have observed a highvariability while using different algorithms and by the use ofdifferent imaging studies. Those algorithms are not justified bycontext differences.TARGET AUDIENCE(S):

1. Clinical researcher2. Guideline developer3. Guideline implementer4. Developer of guideline-based products5. Quality improvement manager/facilitator6. Health care policy analyst/policy-maker7. Health insurance payers and purchasers8. Medical providers and executives9. Consumers and patients representatives

P4– “Best Available” evidence does not mean

“best” studies are available

Danette Stanko-Lopp, MPH (Presenter) (CincinnatiChildren’s Hospital Medical Center, Cincinnati, Ohio)

PRIMARY TRACK: Evidence generation and synthesisSECONDARY TRACK: Evidence appraisalBACKGROUND (INTRODUCTION): To address evi-dence appraisal related to a variety of clinical questions in aninterprofessional atmosphere and to provide simple, transpar-ent evidence appraisal forms, thus improving access to evi-dence evaluation for point-of-care clinicians.LEARNING OBJECTIVES (TRAINING GOALS):

1. Understand evidence appraisal of study for quality.2. Identify the domain of a clinical question and study

designs appropriate for each domain.3. Determine a quality level/grade based on three factors of

domain, study design, and quality appraisal.METHODS: Evidence appraisal forms were developed formultiple study designs specific to each domain. Each appraisalform includes questions about the validity, reliability, andapplicability of a study. Additionally, an appraisal form wascreated to appraise each study design available or possible fora given domain. The multiple study designs by clinical ques-tion domain are captured in a three-dimensional matrix withthe resulting quality level from the appraisal.

80 Otolaryngology–Head and Neck Surgery, Vol 143, No 1S1, July 2010