Improving Adherence to Asthma Guidelines and Asthma ......1. Implement evidence-based asthma...
Transcript of Improving Adherence to Asthma Guidelines and Asthma ......1. Implement evidence-based asthma...
Improving Adherence to Asthma
Guidelines and Asthma Therapies:
Closing the Gap
Supporter – Genentech
Program authors: David A. Beuther, MD, FCCP and Flavia Hoyte, MD
Data From: 09/28/2012 – 09/28/2013
RELEASE DATE: 09/28/2012
VALID FOR CREDIT THROUGH: 09/28/2013
MAXIMUM OF 1.00 AMA PRA CATEGORY 1 CREDIT(S)™
http://www.medscape.org/viewprogram/32600
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Executive Summary An independent educational grant awarded from Genentech included simulation as an educational activity
to address gaps and learning objectives of the physicians treating Asthma. This report summarizes the impact of
the simulation. Decisions made by clinicians within the simulated patient cases are measured and results are
aggregated in the report below.
Gaps The following gaps were identified within the educational grant.
Adherence to asthma diagnosis and management guidelines continues to be suboptimal.
Patient adherence to asthma medications remains suboptimal.
Non-adherence to medications results in reduced asthma control.
New research describes emerging therapies that are not yet covered in current asthma guidelines
Learning Objectives The learning objectives for this simulation are derived directly from the above identified gaps.
1. Implement evidence-based asthma guidelines in their clinical practices and take the steps necessary to
overcome identified barriers
2. Adjust medications to improve asthma control based on domains of both risk and impairment as
described in Expert Panel Report 3 (EPR-3)
3. Facilitate medication adherence in their patients by offering medication regimens individually suited to
patients’ needs and lifestyles
Target Audience The specific audience targeted within the supported educational grant and resulting simulation consisted of
clinicians in the fields of Allergy & Clinical Immunology and Pulmonary Medicine.
Below are the numbers of specialist, and non-specialist (other) users for the two cases in this program:
Case 01: Specialist Users n = 75 Non-specialist users n = 313
Case 02: Specialist Users = n = 21 Non-specialist users = n = 95
Key Findings Clinician performance leaves ample room for improvement on the essential decisions related to tests,
diagnoses, and treatment of both patients.
Simulation users scored the highest on decisions to treat the patient with asthma medications, but failed to
select treatments that would increase disease response and reduce adverse side effects.
Decisions regarding the non-pharmacological management of asthma were especially low, with scores less
than 20% before clinical guidance.
Recommendations for Further Education Based on the above key findings and the analysis provided in detail in this report, the following further
education can be suggested.
Current treatment options according to guidelines for optimizing asthma treatment
Non-pharmacological management that encourages medication adherence and teaches self-
monitoring techniques
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MedSims Patient Cases The case analyses outlined below contain information that the learner is presented with at the introduction
stage of the case. Additional elements of information are made available as they begin their decision making
process and progress through the case.
CASE 01 – Detailed Analyses
Jessica G. Jessica first began treatment for asthma ~4 years ago, when she presented to her primary
care physician complaining of several months of cough, chest tightness, SOB, and malaise.
She noticed these symptoms predominantly while playing basketball. At the time a chest X-
ray showed possible atypical pneumonia. She was treated with an antibiotic and was
diagnosed clinically with asthma. Initial treatment of her asthma was with a short-acting beta
agonist. While Jessica considers her initial treatment to have partially relieved some of her
symptoms, she experienced adverse-effects that made her hesitant to consistently take them. Today, she
presents with dyspnea at rest, and worsening SOB and chest tightness, and palpitations and light-headedness.
Chief Complaint “I am short of breath.”
Current Diagnosis Asthma; Anxiety/stress
Current Medications
Albuterol 90 mcg/inhalation
Alprazolam .25 mg oral tablet
Fluticasone-salmeterol 250 mcg-50 mcg inhalation powder
Vitals Age: 20
BP: 129/84
Height: 169 cm
Weight: 56 kg
BMI: 19.6
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Essential User Decisions: To demonstrate mastery of the learning objectives, users were expected to make the following decisions:
Learning Objective Essential User Decision
1. Implement evidence-based
asthma guidelines in their clinical
practices and take the steps
necessary to overcome
identified barriers
1. Order Methacholine Test
2. Order either Spirometry OR Pulmonary Function Tests
2. Adjust medications to improve
asthma control based on
domains of both risk and
impairment as described in
Expert Panel Report 3 (EPR-3)
5. Continue use of ICS and lower dose
6. Continue use of Rescue Inhaler, but switch to one with
less adverse effects.
7. Facilitate medication
adherence in their patients by
offering medication regimens
individually suited to patients’
needs and lifestyles
1. Order medication adherence counseling
2. Order asthma medication/inhaler Technique
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Case 01 Findings The graph shown below represents data for both specialist and other user groups, and shows data before users
were offered Clinical Guidance. The selected decision points correlate to the established learning objectives
for this CME activity as noted previously.
Complete data tables are presented in the Appendix.
Initial Performance The essential decision points relating to the learning objectives for this case were initially appropriately chosen
by an average of 48% by specialists and an average of 47% by the other users.
13%
12%
64%
65%
48%
81%
15%
13%
57%
67%
49%
87%
0% 20% 40% 60% 80% 100%
Order: Medication/Inhaler Technique
Order: Adherence Counseling
Initiate: Rescue Inhalers
Continue: Inhaled Corticosteroid (ICS)
Order: Methacholine Challenge Test
Order: PFT - OR - Spirometry
LO
3LO
2LO
1
Initial Reinforced Decisions
Specialists n = 75 Others n = 313
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Analysis: Essential tests for this patient were ones that would rule out possible etiologies of her symptoms other than
asthma. Useful for doing so would have been a Methacholine Challenge Test and either Pulmonary Function
Tests (PFT) or a Spirometry. A methacholine challenge test would provide definitive evidence for a diagnosis of
asthma, but was only ordered by 49% of specialists and 48% of other users. Conversely, both sets of users
excelled at the decision to order either PFT or spirometry, with scores of 87% for specialists and 81% for other
users.
A diagnosis was not required for this simulation, since the results of the patient’s workup indicate asthma as the
cause of her symptoms.
The foundation of this case was to adjust and optimize the patient’s asthma treatment. Prior to today’s visit the
patient was taking albuterol and a fluticasone-salmeterol to treat her asthma. For the patient which this case
was based on, the use of albuterol in the initial treatment was not incorrect, but does represent an aggressive
treatment option. In this activity an appropriate decision would have been to swap albuterol for levalbuterol,
as it would cause less jittery sensations. The graph above shows that 57% of specialists and 64% of non-
specialists ordered a rescue inhaler; however, only 9% of specialists and 4% of non-specialists switched to
levalbuterol (see appendix).
Knowledge deficits related to how to administer inhaled corticosteroids and concerning the need to take daily
controller medication for a disease that often feels intermittent to the patient, contribute to poor medication
adherence. Inhaled corticosteroid use is frequently associated with mild-but-irritating adverse effects. These
adverse effects can be reduced but not eliminated through good technique, spacer use if applicable, and
mouth rinsing. For some patients, a major barrier to adherence is the negative stigma of taking "steroids," which
can sometimes be overcome by patient education. Prior to clinical guidance both user groups performed
poorly at the decisions to provide education concerning the use of asthma medications and the management
of adverse side-effects. Less than or equal to 15% of both specialist and non-specialist users initially considered
non-pharmacological treatments essential for optimizing the patient’s asthma control.
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Case 01 Impact of Clinical Guidance Clinical guidance is shown to the user following decision points made throughout the simulation.
The chart below highlights the percentage of participants that initially made the appropriate decision in the
simulation as well as the percentage that did so after receiving educational guidance.
Impact of clinical guidance is displayed here within the Allergy & Clinical Immunology and Pulmonary
Medicine audience groups only.
Complete data tables are presented in the Appendix.
Overall Impact Clinical guidance resulted in a 54% average improvement on essential decisions made by Allergy & Clinical
Immunology and Pulmonary Medicine specialist users.
Analysis The greatest immediate educational impact for specialist users was at the three decisions related to patient
education: adherence counseling (190% change), and asthma medication technique counseling (155%
change).
0% 20% 40% 60% 80% 100% 120%
Order: Adherence Counseling
Order: Medication/Inhaler Technique
Continue: Inhaled Corticosteroid (ICS)
Initiate: Rescue Inhalers
Order: Methacholine Test
Order: PFT - OR - Spirometry
LO
3LO
2LO
1
Specialist Users n = 75
Before CG Add'l After CG
3%
27%
28%
20%
155%
190%
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Case 01 Summary In the case on which this simulation was based, the clinician ordered a methacholine challenge test, which
was very positive, PC[20] of 1.25 mg/mL, thus confirming a diagnosis of asthma. An ECG and echocardiogram
confirmed no significant structural heart disease or cardiac cause of dyspnea. The patient was prescribed
levalbuterol instead of albuterol, which was not completely effective but did cause less jitteriness.
On additional history concerning her asthma medications, it becomes clear that the fluticasone/salmeterol
had been causing significant upper airway adverse effects as well as jitteriness, so she was hesitant to take it
consistently. She knows how to use her inhalers properly and rinses her mouth regularly after administering her
inhaled steroid medication. The patient also considers her symptoms to be episodic and that they do not
warrant daily medication. Finally, she reports severe financial hardship, limiting her access to medications
despite having insurance coverage.
Asthma education, including pathophysiology, medication mechanism of action, and medication usage, was
provided, and Jessica now understands the importance of daily, consistent controller medication use. She was
also educated about and provided with local and industry resources that are available for indigent patients to
obtain lower-cost asthma medications.
Asthma guidelines would assess her as having poorly-controlled, moderate persistent asthma, based upon daily
symptoms. Recommendation is to utilize Step 3 therapy: low-dose ICS/LABA or medium-dose ICS monotherapy.
In this case, her PCP initially prescribed Step 4 therapy, which is not necessarily incorrect but probably is more
than she needed. Given the adverse effects she is experiencing, stepping down to ICS monotherapy may be
preferable.
She was switched from fluticasone/salmeterol to beclomethasone HFA 80 mcg 2 P bid. She had persistent
upper airway adverse effects (hoarse, sore throat) and jitteriness that did not resolve over four weeks, so she
was switched to montelukast 10 mg daily.
At 6 weeks she reported no adverse effects, as well as 60% reduction in cough and dyspnea, no nocturnal
symptoms, infrequent rescue beta-agonist use, and increased activity, although her asthma control test score
only improved to 18 (normal 20-25). Her clinician could have added a low-dose inhaled steroid but did not do
so because the patient was continuing to improve, was afraid of adverse effects, and could not afford to take
two asthma controller medications. Her asthma was well-controlled several months later.
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CASE 02 – Detailed Analyses
Sandra S. Sandra S. is a 43-year-old female with a history of allergies and asthma. She was in the ER last
week for an asthma flare and one of the doctors there told her that she needed to make an
appointment to get better control of her asthma. Despite this recent improvement on
controller therapy, the patient's asthma is "poorly controlled" by EPR-3 guidelines. She is
waking up a couple of times a month due to her asthma, is going to the emergency room
and receiving prednisone once a year on average, her asthma control test (ACT) score is a
13, and she is needing her albuterol inhaler once or twice daily. All of these correspond with poor asthma
control and the need to escalate therapy and evaluate/target any potential co-morbidities
Chief Complaint “The ER doctor sent me here. He said I need help with my asthma.”
Current Diagnosis Obstructive Sleep Apnea; Sinusitis; Osteoarthritis; Obesity; Hypertension; Allergic
Rhinitis; Allergic Conjunctivitis; Seizures; Asthma
Current Medications
Fluticasone 50 mcg/inh nasal spray
Fluticasone-salmeterol 25 mcg-50 mcg inhalation powder
Lisinopril 10 mg oral tablet
Carbamazepine 200 mg oral
Cetirizine 10 mg oral
Albuterol 90 mcg/inh
Vitals Age: 43
BP: 130/82
Height: 165 cm
Weight: 95 kg
BMI: 34.9
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Essential User Decisions: To demonstrate mastery of the learning objectives, users were expected to make the following decisions:
Learning Objective Essential User Decision
1. Implement evidence-based
asthma guidelines in their clinical
practices and take the steps
necessary to overcome
identified barriers
1. Order Methacholine Challenge Test
2. Order Provoked Laryngoscopy
3. Order Pulmonary Function Test
4. Diagnose Gastroesophageal Reflux Disease
5. Diagnose Vocal Cord Dysfunction
2. Adjust medications to improve
asthma control based on
domains of both risk and
impairment as described in
Expert Panel Report 3 (EPR-3)
1. Continue a short-acting beta agonist
2. Step-up therapy
3. Initiate Proton pump inhibitor
3. Facilitate medication
adherence in their patients by
offering medication regimens
individually suited to patients’
needs and lifestyles
1. Allergen avoidance counseling
2. Asthma pathophysiology and medication counseling
3. Speech Therapist counseling
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Case 02 Findings The graph shown below represents data for both specialist and other user groups, and shows data before users
were offered Clinical Guidance. The selected decision points correlate to the established learning objectives
for this CME activity as noted previously.
Complete data tables are presented in the Appendix.
Initial Performance The essential decision points relating to the learning objectives for this case were initially appropriately chosen
by an average of 35% by specialists and an average of 36% for the other users.
20%
1%
73%
76%
5%
11%
45%
21%
76%
29%
5%
67%
71%
10%
24%
19%
19%
76%
0% 20% 40% 60% 80% 100%
Order: Asthma Pathophysiology and MedicationEducation
Order: Speech Therapy
Order: Asthma Step-Up Group
Order: Inhaled Corticosteroid
Diagnose: Vocal Cord Dysfunction
Diagnose: Gastroesophageal Reflux Disease
Order: Methacholine Challenge Test
Order: Provoked Laryngoscopy
Order: Pulmonary Function Tests
LO3
LO2
LO1
Initial Decisions Reinforced
Specialists n = 21
Others n = 95
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Analysis: The users’ first attempts to treat this patient (graphed above) show that both user groups performed less than
average at decisions related to the first learning objective, with the exception of pulmonary function tests.
Perhaps the most definitive test that could have been performed is the methacholine challenge test, which
was only ordered by 19% of specialists and 45% of other users. In addition to an insightful workup for this patient,
simulation users should have diagnosed two comorbidities of asthma: Gastroesophageal reflux disease, and
vocal cord dysfunction. Less than or equal to 24% of all users diagnosed the patient with either of these
conditions.
The patient’s presentation of symptoms at today’s visit indicates by EPR-3 guidelines that she is poorly
controlled. She is waking up a couple of times a month due to her asthma, is going to the emergency room
and receiving prednisone once a year on average, her asthma control test (ACT) score is a 13, and she is
needing her albuterol inhaler once or twice daily. All of these correspond with poor asthma control and the
need to step-up therapy. Treatment options for Sandra include: addition of a leukotriene receptor antagonist,
or addition of omalizumab. Additionally, users could increase the dose of her inhaled steroid, but it would not
be as effective as with a leukotriene inhibitor or omalizumab. The faculty author for this case grouped these
three treatment options as an Asthma Step-Up group. Considered in this way >67% of all users escalated the
patient’s treatment. However, the graph below shows a breakdown of these treatments and a different user
story. Overwhelmingly, specialist users continued the patient’s fluticasone-salmeterol before and after clinical
guidance. Only 5% before, and 10% after chose a leukotriene inhibitor (montelukast), and only 5% chose
omalizumab.
5%
5%
0%
0%
67%
0%
10%
5%
0% 20% 40% 60% 80% 100%
omalizumab
montelukast
zafirlukast
zileuton
fluticasone-salmeterol
32
1
Breakdown of Asthma Step-Up Group
N = 16
Before CG Add'l After CG
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Case 02 Impact of Clinical Guidance Clinical guidance is shown to the user following decision points made throughout the simulation.
The chart below highlights the percentage of participants that initially made the appropriate decision in the
simulation and the percentage that did so after receiving educational guidance.
Impact of clinical guidance is displayed here within the Allergy & Clinical Immunologists and Pulmonologists
audience groups only.
Complete data tables are presented in the Appendix.
Overall Impact Clinical guidance resulted in a 117% average improvement on essential decisions made by specialists.
29%
5%
67%
71%
10%
24%
19%
19%
76%
19%
14%
10%
10%
10%
29%
38%
43%
10%
0% 20% 40% 60% 80% 100%
Order: Asthma Pathophysiology and Medication Education
Consult: Speech Therapy
Order: Asthma Step-Up
Order: Inhaled Corticosteroid
Diagnose: Vocal Cord Dysfunction
Diagnose: Gastroesophageal Reflux Disease
Order: Methacholine Challenge Test
Order: Provoked Laryngoscopy
Order: Pulmonary Function Tests
LO
3LO
2LO
1
Specialist Users n = 21
Before CG % Add'l After CG%
13%
225%
200%
120%
100%
13%
300%
67%
14%
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Analysis Clinical guidance had a major impact on several decision points for this patient. The largest impact was seen
at the decision to schedule a consult with a speech therapist (300% change). Speech therapists trained in
vocal cord dysfunction (VCD) techniques can help patients with VCD learn the breathing techniques they
need to minimize the role of VCD in their respiratory symptoms.
Both diagnoses for the patient saw significant increases. After clinical guidance the diagnosis of
gastroesophageal reflux disease improved by 120% and vocal cord dysfunction by 100%.
Clinical guidance had little impact on the pharmacological treatment of this patient.
Case 02 Summary This patient is a 43-year-old Caucasian female who has a history of allergic rhinitis by skin testing and a clinical
diagnosis of asthma and presents to improve her asthma control given frequent emergency room visits. An
important detail in Ms. S's history is that her asthma and allergies were mild until approximately 8 years ago,
when several changes occurred in her life. She began working in a new hair salon, she moved into an older
house, and she began living with pets for the first time in her life. One or all of these changes worsened her
underlying conditions and should all be evaluated further and targeted. In addition, her asthma worsening has
resulted in frequent prednisone bursts over this time and a decreased ability to exercise due to respiratory
symptoms. These factors have resulted in weight gain, which has led to the development of hypertension,
obstructive sleep apnea, osteoarthritis, and frequent heartburn, none of which she had previously. The
presumed gastroesophageal reflux disease (GERD) that is leading to this heartburn and the obesity itself are
likely leading to worsening of her underlying respiratory symptoms.
In reviewing the patient's asthma history over the past couple of years, it is important to note that she is doing
much better since starting a combined inhaled corticosteroid/long-acting beta-agonist (ICS/LABA). She had
initially been tried on an inhaled steroid, but was not educated regarding the side effects of this medication
class (dysphonia and oropharyngeal candida infection, also called thrush) and proper use of this inhaler (with
an aerochamber followed by rinsing/gargling well) to minimize these side effects. Accordingly, the patient
developed thrush shortly after starting the medication. Thinking she had to choose between improved asthma
control and the "miserable" sensation of the thrush, she decided to discontinue her inhaled corticosteroid.
Several years later, she was prescribed an ICS/LABA, with appropriate education regarding side effects and
proper use. Since then, she has been using the inhaler regularly, with considerable benefit to her asthma, as
evidenced by the decrease in nighttime symptoms and emergency room visits.
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CONCLUSION Overall, simulation users performed below average on all decisions points relating to learning objectives in both
cases.
Learning objective 1 was achieved by an average of 49% by all users in both cases.
Learning objective 2 was achieved by an average of 68% by all users in both cases.
Learning objective 3 was achieved by an average of 17% by all users in both cases.
Although decisions regarding treatment (LO2) for both patients were higher than scores for other decisions,
simulation users failed to make the appropriate decision to optimize treatment and encourage medication
adherence. For Jessica (case 01), the adverse effects of her albuterol interfered with her quality of life leading
her to not consistently use her medication. Users failed to recognize this and the majority continued treatment
with albuterol instead of switching to levalbuterol. For Sandra (case 02), her symptoms were worsening despite
treatment with a mild dose of ICS/LABA combination therapy. The majority of simulation users continued her
treatment with this regimen, but failed to initiate treatment with a more effective prostacyclin, either in addition
to or in place of her current treatment. Similarly, non-pharmacological orders were selected by a small
percentage of users overall. These decisions reflect an oversight by clinicians to recognize the importance of
patient education and counseling in order to promote medication adherence, self-monitoring techniques, and
life-style adjustments.
Future Educational Recommendations According to the data we have collected for this activity, future educational interventions should focus on:
Current treatment options according to guidelines for optimizing asthma treatment
Non-pharmacological orders to encourage medication adherence and to teach self-monitoring
techniques
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METHODOLOGY
Virtual Patient Simulation TheraSim, Inc. is the exclusive simulation provider for Medscape, LLC. Through the power of simulation training,
TheraSim enables healthcare professionals to more rapidly assimilate new medical information and make more
effective clinical decisions.
Learners will be presented with realistic case scenarios to challenge their application of clinical knowledge in
particular indications. Through the simulations learners will make lab, diagnose and therapeutic decisions to
address the virtual patient who sits in front of them.
AIME – Clinical Guidance Supported by the world’s smartest simulation mentor, AIME, learners will receive individual mentoring and
debriefing at every decision point.
Additionally, as a participant ends a patient simulation, the TheraSim Clinical Simulator provides “last chance”
clinical guidance on critical aspects of each case that the participant has either failed to address or addressed
inappropriately.
Case Vignettes Case vignettes have gained considerable support for their value in predicting physician practice patterns.
Results from recent research studies demonstrate that case vignettes (when compared with chart review and
standardized patients) are a valid and comprehensive method of measuring a physician’s process of care in
actual clinical practice. (Luck 2006; Peabody 2000; Peabody 2004)
Furthermore, case vignettes are more cost-effective and less invasive than other means of measurement.
Decision Constraints Diagnostic and therapeutic choices are not constrained – that is, learners can choose from the universe of
possible diagnoses and available drug therapies. As a result, this data can provide insight into the clinical
decisions being made in actual practice.
The analysis for each patient case simulation focuses on those participants that meet the following criteria:
Completed the case
Exhibited engagement with the case by ordering at least one therapy, one drug, or one lab test
Engaged with the debrief section by reviewing case summary, performance analysis, and literature
review
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APPENDIX
Case 01 Impact of Clinical Guidance
Impact of Clinical Guidance: Specialists n = 75
Diagnoses Before CG Add'l After CG Improvement
Asthma, Severe Persistent 3% 0% 0%
Impact of Clinical Guidance: Other Users n = 313
Diagnoses Before CG Add'l After CG Improvement
Asthma, Severe Persistent 10% 1% 6%
Impact of Clinical Guidance: Specialists n = 75
Treatments Before CG Add'l After CG Improvement
Combination ICS/LABA 56% 5% 10%
Cromolyn/Nedocromil 0% 0% inf
Influenza Vaccine 0% 0% inf
Inhaled Corticosteroid (ICS) 67% 13% 20%
Ipratropium 0% 0% inf
LABA 0% 0% inf
Leukotriene Receptor Antagonists (LTRA) 7% 0% 0%
Nasal Corticosteroid Spray 3% 1% 50%
Omalizumab 0% 0% inf
Oral Antihistamine 0% 0% inf
Pneumococcal Vaccine 0% 21% inf
Rescue Inhalers 57% 16% 28%
SABA 57% 16% 28%
Systemic Corticosteroid 3% 0% 0%
Theophylline 1% 0% 0%
Tiotropium 0% 0% inf
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Impact of Clinical Guidance: Other Users n = 313
Treatments Before CG Add'l After CG Improvement
Combination ICS/LABA 51% 5% 9%
Cromolyn/Nedocromil 0% 0% -100%
Influenza Vaccine 0% 5% 1500%
Inhaled Corticosteroid (ICS) 65% 14% 22%
Ipratropium 0% 0% 0%
LABA 0% 1% inf
Leukotriene Receptor Antagonists (LTRA) 9% 1% 7%
Nasal Corticosteroid Spray 4% 3% 82%
Omalizumab 0% 0% inf
Oral Antihistamine 1% 0% 0%
Pneumococcal Vaccine 1% 30% 2375%
Rescue Inhalers 64% 16% 25%
SABA 64% 16% 25%
Systemic Corticosteroid 0% 0% inf
Theophylline 0% 0% inf
Tiotropium 0% 0% 0%
Impact of Clinical Guidance: Specialists n = 75
Labs/Tests Before CG Add'l After CG Improvement
Pulmonary Function Tests (without images) 55% 4% 7%
Electrocardiogram (ECG) 24% 3% 11%
2-D Echocardiogram (Transthoracic) 19% 0% 0%
Chest CT scan 16% 3% 17%
Alpha-1-Antitrypsin Level 23% 3% 12%
Chemistry Screen 19% 0% 0%
Pulse Oximetry - After Walking 32% 20% 63%
Chest X-Ray 61% 12% 20%
Complete Blood Count (CBC) - Basic 39% 4% 10%
Methacholine Challenge Test (MCT) 49% 13% 27%
Pulse Oximetry - At Rest 25% 23% 89%
Spirometry 57% 4% 7%
Total Serum IgE 49% 3% 5%
Asthma Control Test 57% 3% 5%
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Impact of Clinical Guidance: Other Users n = 313
Labs/Tests Before CG Add'l After CG Improvement
Pulmonary Function Tests (without images) 64% 7% 11%
Electrocardiogram (ECG) 38% 4% 9%
2-D Echocardiogram (Transthoracic) 39% 3% 7%
Chest CT scan 24% 3% 11%
Alpha-1-Antitrypsin Level 34% 4% 12%
Chemistry Screen 32% 3% 9%
Pulse Oximetry - After Walking 51% 19% 38%
Chest X-Ray 60% 17% 28%
Complete Blood Count (CBC) - Basic 47% 5% 11%
Methacholine Challenge Test (MCT) 48% 18% 38%
Pulse Oximetry - At Rest 42% 21% 50%
Spirometry 64% 9% 14%
Total Serum IgE 46% 5% 11%
Asthma Control Test 60% 7% 11%
Impact of Clinical Guidance: Specialists n = 75
Non-Pharmacological Before CG Add'l After CG Improvement
Adherence Counseling 13% 25% 190%
Avoidance of Environmental Triggers 12% 24% 200%
Bronchial Thermoplasty 0% 0% inf
Asthma Pathophysiology and Medication Education 12% 8% 67%
Self monitoring of Asthma 16% 19% 117%
Asthma Medication/Inhaler Technique 15% 23% 155%
Allergen Avoidance Counseling 8% 12% 150%
Allergen Immunotherapy 1% 0% 0%
Exercise 9% 4% 43%
Allergy 13% 5% 40%
ENT 1% 0% 0%
Gastroenterology 0% 0% inf
Occupational Medicine consult 0% 0% inf
Pulmonary 0% 3% inf
Speech Therapy 0% 0% inf
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Impact of Clinical Guidance: Other Users n = 313
Non-Pharamacological Before CG Add'l After CG Improvement
Adherence Counseling 12% 34% 274%
Avoidance of Environmental Triggers 12% 34% 297%
Bronchial Thermoplasty 2% 1% 33%
Asthma Pathophysiology and Medication Education 12% 18% 151%
Self monitoring of Asthma 13% 20% 150%
Asthma Medication/Inhaler Technique 13% 34% 250%
Allergen Avoidance Counseling 9% 22% 252%
Allergen Immunotherapy 2% 3% 133%
Exercise 9% 10% 111%
Allergy 6% 4% 63%
ENT 1% 0% 50%
Gastroenterology 0% 0% 0%
Occupational Medicine consult 0% 1% inf
Pulmonary 7% 5% 74%
Speech Therapy 0% 0% 0%
Impact of Clinical Guidance: Specialists n = 75
Case Drugs Before CG Add'l After CG Improvement
omalizumab 0% 0% inf
cromolyn 0% 0% inf
nedocromil 0% 0% inf
methylprednisolone 1% 0% 0%
dexamethasone 0% 0% inf
prednisone 1% 0% 0%
prednisolone 0% 0% inf
theophylline 1% 0% 0%
budesonide-formoterol 4% 0% 0%
formoterol-mometasone 0% 0% inf
fluticasone-salmeterol 52% 5% 10%
formoterol 0% 0% inf
salmeterol 0% 0% inf
ipratropium 0% 0% inf
tiotropium 0% 0% inf
montelukast 7% 0% 0%
zafirlukast 0% 0% inf
zileuton 0% 0% inf
beclomethasone 0% 1% inf
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Impact of Clinical Guidance: Other Users n = 313
Drugs Before CG Add'l After CG Improvement
omalizumab 0% 0% inf
cromolyn 0% 0% -100%
nedocromil 0% 0% inf
methylprednisolone 0% 0% inf
dexamethasone 0% 0% inf
prednisone 0% 0% inf
budesonide 1% 0% 0%
flunisolide 1% 0% 0%
fluticasone 8% 5% 67%
triamcinolone 0% 0% inf
ciclesonide 0% 0% inf
mometasone 0% 1% inf
albuterol 48% 16% 33%
levalbuterol 9% 0% 0%
pirbuterol 0% 0% inf
budesonide nasal 0% 0% inf
fluticasone nasal 0% 0% inf
mometasone nasal 1% 0% 0%
cetirizine 0% 0% inf
chlorpheniramine 0% 0% inf
desloratadine 0% 0% inf
diphenhydramine 0% 0% inf
fexofenadine 0% 0% inf
loratadine 0% 0% inf
pneumococcal 23-valent vaccine 0% 21% inf
influenza virus vaccine, live, trivalent 0% 0% inf
influenza virus vaccine, inactivated 0% 0% inf
metaproterenol 0% 0% inf
albuterol-ipratropium 0% 0% inf
alprazolam 17% 7% 38%
pneumococcal 7-valent vaccine 0% 0% inf
citalopram 0% 0% inf
midazolam 0% 0% inf
warfarin 0% 0% inf
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prednisolone 0% 0% inf
theophylline 0% 0% inf
budesonide-formoterol 2% 0% -17%
formoterol-mometasone 1% 0% -25%
fluticasone-salmeterol 49% 5% 10%
formoterol 0% 0% inf
salmeterol 0% 1% inf
ipratropium 0% 0% 0%
tiotropium 0% 0% 0%
montelukast 9% 0% 0%
zafirlukast 0% 0% inf
zileuton 1% 0% 50%
beclomethasone 4% 2% 64%
budesonide 2% 1% 57%
flunisolide 0% 0% inf
fluticasone 8% 6% 73%
triamcinolone 0% 0% inf
ciclesonide 0% 0% inf
mometasone 0% 0% inf
albuterol 60% 14% 23%
levalbuterol 4% 2% 58%
pirbuterol 0% 0% 0%
budesonide nasal 0% 0% inf
fluticasone nasal 0% 0% inf
mometasone nasal 0% 0% inf
cetirizine 1% 0% 0%
chlorpheniramine 0% 0% inf
desloratadine 0% 0% inf
diphenhydramine 0% 0% inf
fexofenadine 0% 0% inf
loratadine 0% 0% inf
pneumococcal 23-valent vaccine 1% 30% 2375%
influenza virus vaccine, live, trivalent 0% 1% inf
influenza virus vaccine, inactivated 0% 4% 1100%
metaproterenol 0% 0% inf
albuterol-ipratropium 0% 0% inf
alprazolam 24% 2% 7%
pneumococcal 7-valent vaccine 0% 1% inf
citalopram 0% 0% -100%
midazolam 0% 0% 0%
warfarin 0% 0% 0%
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Case 02 Impact of Clinical Guidance
Impact of Clinical Guidance: Specialists n = 21
Diagnoses Before CG Add'l After CG Improvement
Gastroesophageal Reflux Disease (GERD) 24% 29% 120%
Vocal Cord Dysfunction (VCD) 10% 10% 100%
Sinusitis, Chronic 0% 0% inf
Bronchitis, Chronic 0% 0% inf
Impact of Clinical Guidance: Other Users n = 95
Diagnoses Before CG Add'l After CG Improvement
Gastroesophageal Reflux Disease (GERD) 11% 23% 220%
Vocal Cord Dysfunction (VCD) 5% 5% 100%
Sinusitis, Chronic 0% 0% inf
Bronchitis, Chronic 0% 0% inf
Impact of Clinical Guidance: Specialists n = 21
Treatments Before CG Add'l After CG Improvement
ACE-Inhibitor / ARB 57% 5% 8%
Antihistamine 67% 5% 7%
Asthma Step-Up Group 67% 10% 14%
Chronic oral steroid therapy 0% 0% inf
H2 Antagonists 0% 0% inf
Influenza virus vaccination 5% 0% 0%
Inhaled Corticosteroid (ICS) 71% 10% 13%
Inhaled Cortocosteroid add-on therapy 14% 5% 33%
Leukotriene modifying agents 5% 10% 200%
NSAIDs 0% 0% inf
Nasal Steroid 14% 5% 33%
Nasal Steroid Spray 67% 0% 0%
Omalizumab (Anti-IgE receptor) antibody 5% 0% 0%
Proton Pump Inhibitors 10% 43% 450%
S.pneumoniae vaccination 14% 0% 0%
Short acting beta-agonist 67% 10% 14%
Theophylline (Methylxanthines) 0% 0% inf
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anti-epileptics 43% 5% 11%
Impact of Clinical Guidance: Other Users n = 95
Treatments Before CG Add'l After CG Improvement
ACE-Inhibitor / ARB 71% 5% 7%
Antihistamine 73% 5% 7%
Asthma Step-Up Group 73% 12% 16%
Chronic oral steroid therapy 0% 0% inf
H2 Antagonists 0% 0% inf
Influenza virus vaccination 2% 0% 0%
Inhaled Corticosteroid (ICS) 76% 11% 14%
Inhaled Cortocosteroid add-on therapy 0% 2% inf
Leukotriene modifying agents 14% 1% 8%
NSAIDs 0% 1% inf
Nasal Steroid 0% 2% inf
Nasal Steroid Spray 66% 7% 11%
Omalizumab (Anti-IgE receptor) antibody 6% 3% 50%
Proton Pump Inhibitors 8% 28% 338%
S.pneumoniae vaccination 6% 0% 0%
Short acting beta-agonist 77% 12% 15%
Theophylline (Methylxanthines) 0% 0% inf
anti-epileptics 67% 7% 11%
Impact of Clinical Guidance: Specialists n = 21
Labs/Tests Before CG Add'l After CG Improvement
Complete Blood Count (CBC) w/ Differential 52% 0% 0%
Serum Immunoglobulin Measurement 38% 5% 13%
MRI (Brain) 5% 0% 0%
Total Serum IgE (kU/L) 67% 10% 14%
Pre/Post work Peak flows 48% 19% 40%
Exhaled NO (Nitric Oxide) 48% 0% 0%
Asthma Control Test 81% 5% 6%
Pulmonary Function Tests (w/ images) 76% 10% 13%
Chest CT scan 24% 0% 0%
CT Sinuses 62% 5% 8%
Eosinophil Count 33% 0% 0%
Esophagram (Barium Swallow) 33% 5% 14%
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Impedence Probe 10% 0% 0%
Methacholine Challenge Test (MCT) 19% 38% 200%
Provoked Laryngoscopy 19% 43% 225%
Impact of Clinical Guidance: Other Users n = 95
Labs/Tests Before CG Add'l After CG Improvement
Complete Blood Count (CBC) w/ Differential 58% 5% 9%
Serum Immunoglobulin Measurement 35% 6% 18%
MRI (Brain) 17% 3% 19%
Total Serum IgE (kU/L) 58% 6% 11%
Pre/Post work Peak flows 58% 17% 29%
Exhaled NO (Nitric Oxide) 31% 7% 24%
Asthma Control Test 72% 5% 7%
Pulmonary Function Tests (w/ images) 76% 14% 18%
Chest CT scan 28% 3% 11%
CT Sinuses 51% 6% 13%
Eosinophil Count 46% 8% 18%
Esophagram (Barium Swallow) 26% 15% 56%
Impedence Probe 19% 9% 50%
Methacholine Challenge Test (MCT) 45% 15% 33%
Provoked Laryngoscopy 21% 25% 120%
Impact of Clinical Guidance: Specialists n = 21
Non-Pharmacological Before CG Add'l After CG Improvement
Allergen Immunotherapy 43% 0% 0%
Self monitoring of Asthma 43% 10% 22%
Asthma Pathophysiology and Medication Education 29% 19% 67%
Allergen Avoidance Counseling 43% 10% 22%
Asthma Medication/Inhaler Technique 38% 10% 25%
Adherence Counseling 38% 10% 25%
Avoidance of Environmental Triggers 48% 10% 20%
Exercise 33% 5% 14%
Bronchial Thermoplasty 0% 0% inf
Gastroenterology 14% 0% 0%
Speech Therapy 5% 14% 300%
Pulmonary 5% 0% 0%
Occupational Medicine consult 0% 0% inf
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ENT 10% 10% 100%
Allergy 33% 5% 14%
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Impact of Clinical Guidance: Other Users n = 95
Non-Pharamacological Before CG Add'l After CG Improvement
Allergen Immunotherapy 14% 4% 31%
Self monitoring of Asthma 25% 9% 38%
Asthma Pathophysiology and Medication Education 20% 18% 89%
Allergen Avoidance Counseling 28% 16% 56%
Asthma Medication/Inhaler Technique 19% 14% 72%
Adherence Counseling 27% 12% 42%
Avoidance of Environmental Triggers 29% 12% 39%
Exercise 23% 9% 41%
Bronchial Thermoplasty 1% 0% 0%
Gastroenterology 7% 7% 100%
Speech Therapy 1% 9% 900%
Pulmonary 8% 4% 50%
Occupational Medicine consult 1% 2% 200%
ENT 12% 5% 45%
Allergy 22% 8% 38%
Impact of Clinical Guidance: Specialists n = 21
Case Drugs Before CG Add'l After CG Improvement
cetirizine 57% 5% 8%
fexofenadine 5% 0% 0%
desloratadine 5% 0% 0%
loratadine 0% 0% inf
chlorpheniramine 0% 0% inf
levocetirizine 0% 0% inf
diphenhydramine 0% 0% inf
budesonide nasal 0% 0% inf
mometasone nasal 0% 0% inf
fluticasone nasal 67% 0% 0%
triamcinolone nasal 0% 0% inf
ciclesonide nasal 0% 0% inf
beclomethasone 10% 0% 0%
flunisolide 0% 0% inf
theophylline 0% 0% inf
prednisone 0% 0% inf
methylprednisolone 0% 0% inf
omalizumab 5% 0% 0%
fluticasone 0% 5% inf
budesonide 0% 0% inf
mometasone 0% 0% inf
ciclesonide 5% 0% 0%
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montelukast 5% 10% 200%
zileuton 0% 0% inf
zafirlukast 0% 0% inf
naproxen 0% 0% inf
ibuprofen 0% 0% inf
celecoxib 0% 0% inf
flurbiprofen 0% 0% inf
ketoprofen 0% 0% inf
ketorolac 0% 0% inf
meloxicam 0% 0% inf
nabumetone 0% 0% inf
oxaprozin 0% 0% inf
piroxicam 0% 0% inf
sulindac 0% 0% inf
meclofenamate 0% 0% inf
diclofenac 0% 0% inf
cimetidine 0% 0% inf
famotidine 0% 0% inf
nizatidine 0% 0% inf
ranitidine 0% 0% inf
carbamazepine 43% 5% 11%
lisinopril 52% 5% 9%
benazepril 0% 0% inf
captopril 0% 0% inf
enalapril 0% 0% inf
fosinopril 0% 0% inf
irbesartan 0% 0% inf
losartan 5% 0% 0%
quinapril 0% 0% inf
ramipril 0% 0% inf
valsartan 0% 0% inf
perindopril 0% 0% inf
trandolapril 0% 0% inf
candesartan 0% 0% inf
olmesartan 0% 0% inf
telmisartan 0% 0% inf
eprosartan 0% 0% inf
moexipril 0% 0% inf
azilsartan 0% 0% inf
pneumococcal 23-valent vaccine 14% 0% 0%
influenza virus vaccine, inactivated 5% 0% 0%
budesonide-formoterol 0% 5% inf
fluticasone-salmeterol 67% 5% 7%
formoterol-mometasone 5% -5% -100%
triamcinolone 0% 0% inf
albuterol 67% 10% 14%
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levalbuterol 0% 0% inf
dexlansoprazole 0% 0% inf
esomeprazole 5% 0% 0%
lansoprazole 0% 0% inf
omeprazole 5% 43% 900%
pantoprazole 0% 0% inf
rabeprazole 0% 0% inf
acetaminophen 0% 0% inf
Impact of Clinical Guidance: Other Users n = 95
Drugs Before CG Add'l After CG Improvement
cetirizine 68% 4% 6%
fexofenadine 0% 1% inf
desloratadine 0% 0% inf
loratadine 4% 0% 0%
chlorpheniramine 0% 0% inf
levocetirizine 0% 0% inf
diphenhydramine 0% 0% inf
budesonide nasal 0% 0% inf
mometasone nasal 0% 0% inf
fluticasone nasal 65% 7% 11%
triamcinolone nasal 0% 0% inf
ciclesonide nasal 1% 0% 0%
beclomethasone 0% 1% inf
flunisolide 0% 0% inf
theophylline 0% 0% inf
prednisone 0% 0% inf
methylprednisolone 0% 0% inf
omalizumab 6% 3% 50%
fluticasone 0% 0% inf
budesonide 0% 0% inf
mometasone 0% 0% inf
ciclesonide 0% 1% inf
montelukast 14% 1% 8%
zileuton 0% 0% inf
zafirlukast 0% 0% inf
naproxen 0% 0% inf
ibuprofen 0% 0% inf
celecoxib 0% 1% inf
flurbiprofen 0% 0% inf
ketoprofen 0% 0% inf
ketorolac 0% 0% inf
meloxicam 0% 0% inf
nabumetone 0% 0% inf
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oxaprozin 0% 0% inf
piroxicam 0% 0% inf
sulindac 0% 0% inf
meclofenamate 0% 0% inf
diclofenac 0% 0% inf
cimetidine 0% 0% inf
famotidine 0% 0% inf
nizatidine 0% 0% inf
ranitidine 0% 0% inf
carbamazepine 67% 7% 11%
lisinopril 67% 4% 6%
benazepril 0% 0% inf
captopril 0% 0% inf
enalapril 0% 0% inf
fosinopril 0% 0% inf
irbesartan 1% 0% 0%
losartan 1% 1% 100%
quinapril 0% 0% inf
ramipril 0% 0% inf
valsartan 0% 0% inf
perindopril 0% 0% inf
trandolapril 0% 0% inf
candesartan 0% 0% inf
olmesartan 0% 0% inf
telmisartan 1% 0% 0%
eprosartan 0% 0% inf
moexipril 0% 0% inf
azilsartan 0% 0% inf
pneumococcal 23-valent vaccine 6% 0% 0%
influenza virus vaccine, inactivated 2% 0% 0%
budesonide-formoterol 4% 0% 0%
fluticasone-salmeterol 72% 9% 13%
formoterol-mometasone 0% 1% inf
triamcinolone 0% 0% inf
albuterol 77% 12% 15%
levalbuterol 0% 0% inf
dexlansoprazole 0% 0% inf
esomeprazole 0% 6% inf
lansoprazole 0% 3% inf
omeprazole 7% 15% 200%
pantoprazole 1% 3% 300%
rabeprazole 0% 1% inf
acetaminophen 1% 0% 0%
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REFERENCES
Luck J, Peabody JW, Lewis BL. An automated scoring algorithm for computerized clinical vignettes: evaluating
physician performance against explicit quality criteria. Int J Med Inform. 2006;75:701-707.
Peabody JW, Luck J, Glassman P, Dresselhaus TR, Lee M Comparison of vignettes, standardized patients, and
chart abstraction: a prospective validation study of 3 methods for measuring quality. JAMA.
2000;283:1715-1722.
Peabody JW, Luck J, Glassman P, Jain S, Hansen J. Measuring the quality of physician practice by using
clinical vignettes: A prospective validation study. Ann Intern Med. 2004;141:771-778.
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