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POPULATION HEALTH MANAGEMENT

Volume 12, Number 2, 2009


ª Mary Ann Liebert, Inc.
DOI: 10.1089=pop.2008.0021

Asthma: Are We Monitoring the Correct Measures?

William J. Cardarelli, R.Ph.

Abstract

The prevalence of asthma, a common chronic inflammatory disease of the airways, has risen sharply over the
past 25–30 years, with the biggest increase found in children. Currently, more than 22 million Americans have
asthma. Asthma also is associated with significant morbidity and mortality worldwide. Each year, asthma is
responsible for $16 billion in direct and indirect costs due to health care utilization and loss of productivity, with
over 14 million missed workdays. Asthma also accounts for almost 1.8 million emergency room visits and almost
500,000 hospitalizations annually. Therefore, assessment and monitoring of disease activity is critical to improve
clinical and economic outcomes for patients with asthma. To help in this endeavor, practitioners and payers rely
on evidence-based guidelines to classify disease severity, to guide treatment decisions, and to assess the degree
of asthma control. In August 2007, the National Asthma Education and Prevention Program (NAEPP) updated
its guidelines based on greater knowledge of disease pathophysiology and the development of newer thera-
peutic agents. This includes an increased emphasis on the need to establish disease severity, including the
components of impairment and risk, as well as on the level of asthma control. Despite the availability of the
NAEPP and other guidelines, asthma control often remains suboptimal. While numerous clinical and patient-
reported measures are available, it is clear that the optimal monitoring schema for patients with asthma remains
undefined. To clearly establish whether asthma control is attained, multiple measures are required and should
include clinical and patient-reported assessments. (Population Health Management 2009;12:87–94).

Introduction dust), and other inhaled irritants—are diverse and can pro-
duce symptoms that range from transient to life-threatening
episodes of respiratory distress.1 Due to the variable nature
A sthma is characterized by chronic airway inflam-
mation, airway hyperreactivity, reversible airway ob-
struction, and airway remodeling secondary to chronic
of asthma, the degree of disease severity, including the do-
mains of functional impairment and risk of future exacer-
airway inflammation.1,2 For most patients, asthma is an epi- bations, is an important consideration. Equally important is
sodic disease with periods of relative stability punctuated by the need to monitor control constantly to ensure optimal
episodes of disease exacerbation. Whereas inflammation is outcomes and improve the overall quality of life (QOL) of
responsible for the underlying disease pathology, the causes asthma patients.
and etiology of asthma are multifactorial. Emerging evidence Recently updated guidelines from the National Asthma
demonstrates there is considerable variability in the pattern Education and Prevention Program Expert Panel Report 3
of inflammation, indicating differences in phenotypes that (NAEPP EPR-3) emphasize the need for a comprehensive
could potentially affect treatment response.3 Genetic (ie, pre- approach to asthma management to include assessment and
disposition to developing anti-immunoglobulin E-mediated monitoring, education, control of environmental and other
response to common aeroallergens) and environmental fac- factors that affect asthma, and patient and provider educa-
tors, particularly allergic reactions, have been linked to the tion.3 Despite the availability of multiple guidelines to assist in
disease.2,3 the diagnosis and management of asthma, control is subop-
Symptom manifestation may vary from patient to patient, timal for many patients. This may be attributable to the fact
with shortness of breath, cough, tightness of the chest, spu- that providers may be relying primarily on clinical measures
tum production, and wheezing considered hallmark symp- to determine asthma severity and control, thus potentially
toms of asthma. Disease exacerbations—caused by a under-recognizing patients who have severe uncontrolled
multitude of factors including viral infections, allergy, exer- asthma. The NAEPP guidelines recommend an approach that
cise, airborne irritants (ie, cigarette smoke, strong odors, includes clinical and patient-reported measures to obtain an

Atrius Health=Harvard Vanguard Medical Associates, Watertown, Massachusetts.

87
88 CARDARELLI

accurate assessment of asthma’s impact on patient QOL.3 This ducted by Zhang and colleagues that assessed the relation-
could lead to identifying those who have severe uncontrolled ship of several asthma control end points, the investigators
asthma, who are high utilizers of health care resources. concluded that the relationship among variables is complex
and a simple definition of asthma control is not possible;
Clinical Guidelines multiple measurements over a long period are needed to
create a more precise picture of asthma control and patient
Evidence-based clinical guidelines serve as current stan-
response.13
dards of practice for the management of patients with asth-
Currently there are numerous available measures of
ma.3–5 Both the Global Initiative for Asthma and the NAEPP
asthma control. Each has strengths and weaknesses (Table 1),
guidelines provide practitioners with diagnostic parameters,
so it is likely that incorporation of more than 1 of these
treatment modalities, strategies for assessment and moni-
measures is necessary to provide an accurate assessment of
toring, and patient education.3 Pulmonary function mea-
asthma control. This strategy will provide a much broader
surements, frequency of beta-agonist use, daily symptoms,
picture of overall symptom management. It also will enable
and nighttime awakenings are used to establish disease se-
clinicians and managed care organizations (MCOs) to better
verity and to measure the effectiveness of therapy.3 The
identify those with severe or uncontrolled asthma and to
NAEPP guidelines clearly differentiate between assessment
potentially develop treatment strategies that can lead to
and monitoring and the close link between severity, control,
optimal disease control.
and treatment response. The concept of control is also further
delineated into degrees of reducing impairment (ie, func-
tional limitations due to asthma symptoms) and risk (ie, Measures of pulmonary function=hyperreactivity
future asthma exacerbations or decline in lung function in
Measurement of pulmonary function with forced expira-
adults or reduced lung growth in children).3
tory volume in 1 second (FEV1) is often used to monitor
Although the guidelines provide a classification system for
patients with asthma. FEV1 is generally accepted as the
asthma severity, both patients and physicians tend to un-
standard clinical measure of airway flow and obstruction in
derestimate the severity of disease.6,7 Perhaps this discrep-
patients with asthma.6,14,15 This test is considered an objec-
ancy persists because the inflammatory process is complex
tive and reliable measure of airflow with reproducibility
and symptoms can vary from patient to patient, from day to
upon repeat testing.10 Efficacy outcomes and measures of
day, and throughout the day.
therapeutic success in clinical trials most often rely on
Based on previous guidelines, questions arose about
changes in FEV1 following the introduction of therapy as a
classifications of asthma severity after treatment and which
measure of asthma control.16
aspects of asthma should be monitored. The 2007 NAEPP
A consensus on the optimum number and timing of FEV1
guidelines clarify this by noting that initial treatment should
measurements has not been established and can vary with
be based on disease severity at diagnosis. After therapy has
each study design, making interpretation of the results of
been initiated, emphasis should be on how well asthma is
multiple studies difficult. Furthermore, while this test offers
controlled relative to therapeutic goals and any appropriate
insight into airflow changes, the patient-perceived effects of
adjustments to obtain the desired outcome. The American
an intervention and subsequent symptom control do not
Academy of Allergy, Asthma & Immunology and the
necessarily strongly correlate with FEV1 changes.16,17
American College of Allergy, Asthma, and Immunology
The NAEPP now recommends using the ratio of FEV1 and
recommend that asthma management be driven by treat-
forced vital capacity (FVC) to assess asthma severity and
ment decisions based on assessment of control.8
control in patients aged 5 years and older, and includes
suggested ranges for these measurements in its updated
Monitoring Asthma Control
guidelines. This change was made because FEV1=FVC may
Periodic monitoring of asthma control is an essential be a more sensitive measure than FEV1 alone.3
component of the NAEPP guidelines. The NAEPP defines Peak expiratory flow (PEF) rate also has been used as a
the level of asthma control as ‘‘the degree to which both measure of pulmonary obstruction. An advantage of mea-
dimensions of the manifestations of asthma—impairment suring PEF is the ability of the patient to assess pulmonary
and risk—are minimized by therapeutic intervention.’’3 function at home with a simple and inexpensive PEF meter.
It is also important to recognize the distinction between It has been suggested that PEF can be used to assess bron-
asthma severity and disease control.9,10 However, universal chodilator response as the specificity and sensitivity allows
use of available objective measures may not accurately reflect for accurate, reliable measures. However, this measure is not
disease severity and control in the presence of active treat- reliable when measuring bronchoconstriction following meth-
ment. Variability of patient disease severity and heteroge- acholine challenge.15 Additional data question the reliability
neity of the population further limit the utility of these tests of this measure and report that it underestimates the severity
in the overall asthma population. Interpatient and in- of airflow obstruction.18 Over time, patient compliance with
trapatient differences make it difficult to apply the current long-term measurement of PEF with PEF meters diminishes,
classification system universally and to employ a single, producing a less than accurate assessment of the patient’s
simple monitoring parameter for patients with asthma.7,11 status.19 The NAEPP emphasizes that peak flow and symp-
Traditionally, pulmonary function measures, symptoms tom-based monitoring, if taught and followed correctly, can
scores, and rescue medication use are measures to assess be equally effective.
patients’ medication needs to treat asthma. However, these Bronchial hyperresponsiveness (BHR), a characteristic of
measures do not necessarily correlate with improvements in patients with asthma, produces symptoms of chest tightness,
the patient’s functional status (ie, QOL).12 In a study con- breathlessness, and wheezing. BHR can be measured
Table 1. Asthma Monitoring Strategies

Monitoring strategy Advantages Disadvantages Place in therapy

Measures of pulmonary function=hyperreactivity


FEV1 Standard measure of airflow Circadian variation Measure of efficacy
and obstruction Optimum number of measures= in clinical trials
Measures airflow from both day and timing of Used to diagnose asthma
large and peripheral airways measurements ill defined
Objective and reliable No correlation between
Reproducible patient-perceived effects
Expensive
Inconvenient for patients
FEV1=FVC May be a more sensitive
measure than
FEV1 alone
PEF Standard measure of Primarily a measure of Used for ongoing
pulmonary obstruction large airways monitoring
Simple and inexpensive May underestimate the severity Routine monitoring
Accurate and reliable measure of airflow obstruction suggested for patients
of bronchodilator response Reliability has been questioned with moderate to
Convenient for patients Patient compliance severe asthma
decreases with time
Optimum number of measures=
day and timing of
measurements ill defined
BHR Standardized Expensive Diagnostic measure
Highly sensitive for Labor intensive for asthma
asthma diagnosis Inconvenient for patients Potentially useful
Provides information adjunctive measure
into underlying of patient response
inflammatory process to anti-inflammatory
treatment
Measures of airway inflammation
Sputum eosinophil Accurate measure of Time consuming Useful for predicting
counts airway inflammation asthma deterioration
Noninvasive
Exhaled NO Simple No correlation between Potentially useful
Noninvasive FEV1 and QOL adjunctive measure
Repeatable measure of airway Larger studies need of patient severity
hyperresponsiveness to determine role and response to
Technique standardized treatment
in children
Serum IgE Provides insight into Requires physician office visit Identify candidates for
disease activity Invasive anti-IgE treatment
Monitoring response to
anti-IgE treatment
Additional measures of asthma control
Exacerbation frequency Useful measure of patient’s Inconsistencies in data Important indicator of
overall asthma control due to changes asthma control
Does not require in health plan, polypharmacy,
additional testing and poor follow-up
QOL Offers patient perspective Not a traditional measure Adds information about
Many tools have of therapy effect functional status
been validated Correlation between QOL score Focuses on issues
and severity of asthma important to patients
not consistent
Symptom scoring tools Offers patient perspective Many available tools have Identify potential
Can be used to predict not been validated improvements in
asthma outcomes Weak correlation with FEV1 asthma therapy
May be difficult to score No consensus on
the best tool

BHR, bronchial hyperresponsiveness; FEV1, forced expiratory volume in 1 second; FVC, forced vital capacity; IgE, immune globulin E; NO,
nitric oxide; PEF, peak expiratory flow; QOL, quality of life.
90 CARDARELLI

through standardized bronchoprovocation tests that use asthma deterioration following a discontinuation of inhaled
pharmacologic (ie, methacholine, histamine, mannitol, corticosteroid.30 These tests often are time consuming (in-
adenosine monophosphate, hypertonic saline) or natural duction of sputum requires coughing into a sterile container
(exercise) challenges.20,21 Bronchoprovocation tests are for several minutes) and at present, use remains limited to
highly predictable for the diagnosis of asthma and are con- clinical studies or for evaluation of difficult-to-treat patients.32
sidered highly sensitive.
Methacholine and histamine challenges are considered Additional measures of asthma control
direct stimuli that produce bronchoconstriction in individu-
A primary goal of asthma therapy is the reduction of risk,
als without asthma, although the degree of bronchocon-
which includes prevention of recurrent exacerbations and
striction is greater in patients with asthma.20,22,23 Indirect
progressive loss of lung function (in children, the prevention
stimuli (ie, mannitol, adenosine monophosphate, hypertonic
of reduced lung growth), and the optimization of pharma-
saline, exercise) cause a release of preformed inflammatory
cotherapy with minimal or no side effects.3 Longitudinal
mediators and offer insight into underlying inflamma-
assessment using spirometry is necessary to measure risk of
tion.20,23 Following provocation challenge, a 20% decrease in
progressive loss of lung function; in children, the risk for
FEV1 from baseline is considered diagnostic for asthma.
reduced lung growth is assessed by prolonged failure to at-
Beyond diagnosis, the role of BHR testing in the man-
tain predicted lung function values for age.3
agement of asthma has been investigated.20,24,25 Unlike FEV1
However, clinical measures alone may not be sufficient to
and PEF, indirect bronchoprovocation challenges provide
determine the full impact of asthma on the patient’s daily
information about the underlying inflammatory process.20
functioning and limitation of activities. Therefore, patient-
Because decreases in airway hyperresponsiveness have cor-
reported measures can further guide the clinician in identi-
related with a decrease in eosinophil response and are a
fying those individuals with severe uncontrolled asthma
measure of the inflammatory process, these tests may be a
who may require more intensive management and treat-
useful adjunct for monitoring patient response to therapy
ment. The use of these measures may also be helpful to de-
and determining if pharmacotherapy measures are control-
termine which patients are at future risk of exacerbations and
ling the inflammatory process.20,21
have the potential to become greater consumers of health
care resources.
Measures of airway inflammation Symptom-scoring measures rely on patient perception of
asthma control and may not always reflect disease control as
Recognition of asthma as an inflammatory disease has
measured with objective tools. A study by Zhang concluded
increased interest in monitoring tools that measure inflam-
that FEV1 and daily symptoms score showed only a weak
matory activity. Exhaled nitric oxide (NO) levels increase in
correlation, suggesting that they measure different asthma end
patients with asthma following allergen challenge and dur-
points and that improvement in one parameter cannot be ex-
ing exacerbations.26 Evaluation of airway inflammation
trapolated to overall improvement.13 Although various tools
through exhaled NO offers a simple, noninvasive, repeatable
for measuring patient control have been correlated to positive
measure of airway hyperresponsiveness and has been pro-
outcomes, there is no consensus on the most appropriate
posed as an adjunct measure to determine the severity of
measures to include. Therefore, the NAEPP recommends using
asthma and response to therapy.27 The technique for mea-
both approaches to ensure optimal asthma management.
suring exhaled NO has been standardized for children and
reference values are available.28
Patient-Reported Asthma Measures
In addition, preliminary investigation in a small group of
patients indicates that other inflammatory markers (ie, IL-6, The Asthma Control Test (ACT), a validated measure for
IL-4) are elevated in the breath of patients with asthma.29 those with mild to moderately severe asthma, is used to
Results from this study indicate that exhaled IL-4 levels, but identify patients with poor disease control.34 This patient-
not IL-6, decreased following treatment with inhaled steroids, based questionnaire consists of 5 questions that ask the pa-
suggesting that exhaled IL-4 concentrations may be an adjunct tient to assess their level of asthma control during the past
measure for assessing patient response to therapy.29 Exhaled 4 weeks. This questionnaire, which encompasses asthma
IL-4 and IL-6 did not correlate with FEV1, however.29 symptoms, use of rescue medications, and the impact of
Eosinophils are important inflammatory markers found in asthma on everyday function, is considered reliable and easy
the sputum of patients with asthma. Eosinophil levels are to use. Patients who score 19 on this test are considered to
increased during exacerbations and are reduced in response have uncontrolled asthma. Initial results with this tool indi-
to anti-inflammatory medications.30–32 Although eosino- cate a stronger correlation between the ACT score and an
philia is also seen in the peripheral blood of patients with asthma specialist’s assessment of the patient than FEV1 re-
asthma, sputum eosinophil counts are considered more ac- sults and the specialist’s assessment.34 Additionally, ACT
curate than serum evaluations.33 In the past, sputum eosin- provides a more simplified assessment of asthma control
ophil evaluations in patients with asthma were reserved for because FEV1 is not required, which is beneficial in settings
clinical study and required the use of invasive broncho- where FEV1 is not available.34 Schatz et al demonstrated that
alveolar lavage. Now, simple noninvasive sputum tests are ACT scores were responsive to changes in asthma control
available with results similar to those reported with invasive over time for patients new to the care of an asthma specialist,
procedures—bronchoalveolar lavage and bronchial wash. indicating that the test might be essential for managing
The results of sputum analysis are considered accurate en- asthma patients during the course of their disease.35
ough to use as a guide to adjust anti-inflammatory medica- The Asthma Therapy Assessment Questionnaire (ATAQ)
tions (inhaled corticosteroids) and can be used to predict was developed as a disease management tool to identify
MONITORING ASTHMA 91

patients whose asthma is not optimally managed.36 This portant to include the impact of a medication on QOL when
brief, self-administered questionnaire comprises 5 questions measuring its overall effect. Patient perceptions of improve-
to assess asthma control in general; missed days of work, ment often are not accurately reflected in the clinical as-
school, or normal activities; nighttime awakening; and the sessment of a therapy.16 Health-related quality of life
need for rescue medications. Higher scores on this test in- (HRQOL), like symptom scoring, incorporates the patient’s
dicate greater levels of uncontrolled asthma. The ATAQ perspective into the measure of asthma therapy. HRQOL
correlates highly with self-reported QOL and is predictive of tools help to measure the effects of asthma on the patient’s
future acute care episodes.36,37 In a study by Peters et al, the functional status and incorporate the patient’s satisfaction
ATAQ control index helped to identify patients without re- with therapy into the overall assessment. Until recently, QOL
cent acute care who had a 6-fold greater risk for future acute measures to assess efficacy of therapy were not used con-
health care utilization.38 The authors also state that, when sistently in clinical trials.
used in conjunction with administrative claims data, the The effect of asthma therapy on patient functional status
ATAQ can be useful in predicting future health care utili- and reduction of symptoms are important QOL parame-
zation, which could be helpful to clinicians and organiza- ters.12,44 The Asthma Quality of Life Questionnaire (AQLQ)
tions interested in population-based disease management.38 and the Pediatric Asthma Quality of Life Questionnaire
Other measures that have been validated include the (PAQLQ) have been validated and are considered reliable
Asthma Control Questionnaire (ACQ) and Asthma Control measures of QOL.12,44–47
Diary.39 The ACQ comprises 6 questions to determine asth- The AQLQ is a clinician-administered measure that asks
ma control. This validated instrument addresses symptom patients to assess the impact of their asthma over a 2-week
severity of asthma patients (ie, wheezing, shortness of period. This questionnaire contains 32 items, including a list
breath), as well as nighttime awakenings, severity of symp- of daily activities, designed to assess the degree of impair-
toms on awakening, limitations to daily activities, and ment due to their asthma in 4 domains: symptoms, activity
number of daily puffs with a short-acting bronchodilator.40 limitation, emotional function, and environmental stimuli.
The ACQ also includes FEV1 measurement, performed by a This scale asks the patient to rate on a 15-point scale (-7 to 7)
member of the health care team, to further determine a pa- how asthma has limited their activities in the previous
tient’s asthma control. A study by Juniper et al validated the 2 weeks. Designed to detect small within-subject changes,
use of this instrument to identify patients whose asthma the AQLQ is reproducible even when the patient’s asthma is
is poorly controlled.40 After utilizing this instrument for 9 stable.44 For patients whose asthma is inadequately con-
weeks, the authors found that the ACQ has strong mea- trolled with medication, the AQLQ, in addition to clinical
surement properties as an evaluative and discriminative in- measures, is useful to measure HRQOL in adults with
strument. Additionally, completion of the ACQ in the asthma.44,45
waiting room may save consultation time and could be used The PAQLQ is a 23-item questionnaire designed to de-
to enhance disease management, possibly reducing health termine the burden of illness in children aged 7 to 17 years.
care resource utilization for this population.40 The Asthma This simple, easy-to-use questionnaire looks at 3 domains
Control Diary is a validated, easy-to-use instrument that asks related to the impact of asthma on activity limitation,
patients to record asthma severity upon awakening and at symptoms, and emotional function.46 This instrument uses a
bedtime; the criteria used for this evaluation are similar to scale of 1 to 7, with lower scores indicating a greater degree
those of the ACQ. Instead of FEV1 measurement by office of uncontrolled asthma. Additionally, the PAQLQ asks pa-
staff, however, patients are asked to record their PEF rates.41 tients to identify 3 activities (from a list of 35) in which
Both the ACQ and Asthma Control Diary are useful for asthma has limited their ability to perform. This instrument
measuring asthma control; the reliability and responsiveness was able to detect change in children who improved and
of the ACQ, however, is better than use of a diary.41,42 those who deteriorated, and to distinguish between those
Another validated instrument is the Asthma Control who had minor and more serious QOL impairments.46
Score, an easy-to-use scoring system based on a percentage The NAEPP also identifies the Mini Asthma Quality of
of optimal control for clinical, physiological, and inflamma- Life Questionnaire (MiniAQLQ), the Integrated Therapeutics
tory assessments.43 The clinical components focus on diurnal Group Asthma Short Form (ITG-ASF), and the Asthma
and nocturnal symptoms, b2-agonist use, and limitation to Quality of Life for Children validated instruments for the
physical activity; the physiologic assessment looks at FEV1 or assessment of asthma-specific QOL. A correlation between
PEF, as well as PEF variation; the inflammatory component mild asthma, as defined by lung function, symptoms, and
evaluates the percentage of airway eosinophilia. The Asthma reliever medication use, and the AQLQ score has been con-
Control Score is a simple, practical, and flexible instrument firmed; however, this correlation did not hold for patients
that can be used by patients, providers, and researchers to whose asthma is moderate to severe.16
determine asthma control.43 Another advantage is that this The MiniAQLQ is a reliable, validated measure to ascer-
instrument incorporates 3 of the most typical asthma mani- tain QOL impairments due to asthma. The MiniAQLQ is a
festations: respiratory symptoms, changes in expiratory self-administered 15-question instrument that evaluates the
flows, and airway inflammation.43 same 4 domains as the AQLQ. In a clinical study, scores
between the 2 measures were similar in detecting the burden
of illness; however, between-visit scores were not as consis-
Quality of Life
tent with the MiniAQLQ.48
Asthma is a chronic disease that may affect a patient’s The ITG-ASF is a brief, comprehensive, 15-item ques-
ability to participate in normal daily routines including tionnaire designed to evaluate the impact of asthma on an
work, school, and extracurricular activities. Thus, it is im- easy 5-point scale (from not at all to very severely). The
92 CARDARELLI

questionnaire, designed for those aged 14 years and older, assessing disease severity and monitoring for control when
asks patients to respond to questions that correspond to 5 evaluating patient response to treatment. Assessing the im-
parameters: symptom-free index, functioning with asthma, pact of asthma therapy must include parameters that mea-
psychosocial impact, asthma–confidence in health, and sure changes in lung function and control of disease,
asthma energy.49 The ITG-ASF Total showed greater re- including impairment and risk. Effective monitoring tools
sponsiveness to lung function changes and number of are vital to ensure that clinicians have a complete picture of
workdays missed than the AQLQ, but was less responsive at the patient with asthma. Therefore, it is important to con-
showing changes in NAEPP and patient-related asthma se- tinually evaluate existing tools to determine if their mea-
verity than the AQLQ. This validated and reliable measure, surements truly correlate with asthma severity and control.
however, is a good adjunct to traditional clinical measures A single optimal test for monitoring asthma patients does
(ie, FEV1) and generic outcomes measures (ie, Short Form-36) not exist, however, and combinations of available measures,
in determining the burden of asthma.49 including those that account for the patient’s view of asthma
The recently released NAEPP EPR-3 guidelines emphasize control, provide a more accurate picture of disease activity.
the importance of assessment to determine disease severity, Patient self-reporting that targets symptom severity, reduced
including risk of future exacerbations and impairment of activities, emergency department use, and hospitalization
daily activities, as well as ongoing monitoring to determine can be used to predict asthma outcomes for diverse patient
therapeutic effectiveness on asthma control. FEV1=FVC is a populations. Based on patient questionnaire results, risk
reliable measure that enables physicians to determine disease models can be developed to identify patients at risk for in-
severity and provides a road map regarding what treat- creased asthma symptoms, disability, and avoidable use of
ment(s) may be most appropriate based on the guideline’s health care resources. As more weight is given to patient-
recommended step-care approach. In addition, clinicians can perceived symptoms, instruments that include patient
use the ACT to gain the patient’s perceptions of disease se- assessment of disease activity could provide valuable infor-
verity and control and compare them with the FEV1=FVC mation regarding asthma symptoms and control and identify
results. This also provides clinicians with an opportunity opportunities to improve asthma management.
to educate patients about the importance of disease self- Asthma is a therapeutic area in which the managed care
management (eg, minimizing or eliminating factors that may community can make a substantial positive contribution to
exacerbate their disease), how to recognize when their dis- improving the overall care of this patient population. MCOs
ease is uncontrolled, and about the importance of medication have access to both cost and health care utilization infor-
adherence. For payers, baseline assessment of disease se- mation and can use these data to identify those patients who
verity can help identify patients with severe persistent are at the highest risk. Communicating this information to
asthma who may be high utilizers of health care resources. their provider network will help physicians deliver better
These patients can then be targeted for more aggressive care management to their patients. In addition, many MCOs
treatment, which may decrease the use of rescue medica- publish member newsletters several times a year, which
tions, as well as office=emergency department visits and could be used to educate members about asthma manage-
hospitalizations. ment and the importance of medication adherence. This
For maintaining asthma control, employing the ACT on newsletter could also include a simple screening tool, such as
follow-up visits will provide physicians with ongoing patient the ACT, to help members to self-manage their disease.
insights regarding asthma control. Greater patient monitor-
ing could be achieved through PEF, an inexpensive method Acknowledgments
to determine control. This measure must be supplemented
with the use of a patient diary, however, to identify factors The author wishes to acknowledge Charlotte Kenreigh
that can precipitate or exacerbate symptoms. These data can and Deborah Lee Ross, medical writers, Strategic Healthcare
help clinicians reevaluate and update their pharmacologic Alliance, for their assistance with the writing and researching
strategy, as appropriate, and enable continued physician- of this manuscript. The author also wishes to acknowledge
patient discussion about how patients can effectively manage Dennis Bloshuk, editor, Strategic Healthcare Alliance, for his
their disease. This ongoing discussion is beneficial to payers assistance with the editing and preparing of this manuscript.
because better overall management by clinicians and pa-
tients, including increased medication adherence, can im- Disclosure Statement
prove outcomes and reduce the need for rescue medications,
office=emergency department visits, and hospitalizations. The author discloses no significant financial relationships
or affiliations.

Conclusion References
Asthma is a dynamic inflammatory disease with multiple 1. Fireman P. Understanding asthma pathophysiology. Allergy
factors that contribute to its severity at any particular point Asthma Proc 2003;24:79–83.
in time. The impact of asthma is far-reaching and varied, 2. Maddox L, Schwartz D. The pathophysiology of asthma.
with physical, social, and economic consequences. As with Annu Rev Med 2002;53:477–498.
other chronic diseases, it is important to monitor disease 3. National Heart, Lung and Blood Institute. Expert Panel Re-
activity over time to identify patients whose disease is port 3: Guidelines for the diagnosis and management of
worsening and=or determine patient response to therapeutic asthma. Full report 2007. NIH Publication No. 07-4051. Be-
interventions. The current guidelines stress the importance of thesda, MD: National Institutes of Health; 2007.
MONITORING ASTHMA 93

4. Global Initiative for Asthma. Pocket Guide. Available at: 23. Joos G. Bronchial hyperresponsiveness: Too complex to be
http:==www.ginasthma.org=Guidelineitem.asp??l1¼2&l2¼1& useful? Curr Opin Pharmacol. 2003;3:233–238.
intId¼37. Updated December 2006. Accessed November 16, 24. Sont J, Willems L, Bel E, van Krieken JH, Vandenbroucke JP,
2007. Sterk PJ. Clinical control and histopathologic outcome of
5. National Asthma Education and Prevention Program. Ex- asthma when using airway hyperresponsiveness as an ad-
pert Panel Report: Guidelines for the diagnosis and man- ditional guide to long-term treatment. Am J Respir Crit Care
agement of asthma—Update on selected topics 2002. NIH Med 1999;159:1043–1051.
Publication No. 02-5074. Bethesda, MD: National Institutes 25. Van Schoor J, Joos G, Pauwels R. Indirect bronchial hyperre-
of Health; 2003. sponsiveness in asthma: Mechanisms, pharmacology and
6. Fuhlbrigge A, Adams R, Guilbert T, Grant E, Lozano P, implications for clinical research. Eur Respir J 2000;16:514–533.
Janson SL, Martinez P, Weiss KB, Weiss ST. The burden of 26. Lúdviksdóttir D, Janson C, Hogman M, Hedenstrom H,
asthma in the United States. Am J Respir Crit Care Med Björnsson E, Boman G. Exhaled nitric oxide and its rela-
2002;166:1044–1049. tionship to airway responsiveness and atopy in asthma.
7. Calhoun W, Sutton L, Emmett A, Dorinsky P. Asthma var- Respir Med 1999;93:552–556.
iability in patients previously treated with ß2-agonists alone. 27. Colice G. Categorizing asthma severity and monitoring
J Allergy Clin Immunol 2003;112:1088–1094. control of chronic asthma. Curr Opin Pulm Med 2002;8:4–8.
8. Joint Task Force on Practice Parameters. American Academy 28. Brand P, Roorda R. Usefulness of monitoring lung function
of Allergy, Asthma and Immunology; American College of in asthma. Arch Dis Child 2003;88:1021–1025.
Allergy, Asthma and Immunology and Joint Council of 29. Carpagnano G, Barbaro M, Resta O, Gramiccioni E, Valerio
Allergy, Asthma and Immunology. Attaining optimal asth- NV, Bracciale P, Valerio G. Exhaled markers in the moni-
ma control: A practice parameter. J Allergy Clin Immunol toring of airways inflammation and its response to steroid’s
2005;116:S3–S11. treatment in mild persistent asthma. Eur J Pharmacol. 2005;
9. Vollmer W. Assessment of asthma control and severity. Ann 519:175–181.
Allergy Asthma Immunol 2004;93:409–414. 30. Deykin A, Lazarus S, Fahy J, Wechsler ME, Boushey HA,
10. Fuhlbrigge A. Asthma severity and asthma control: Symp- Chinchilli VM, Craig TJ, Dimango E, Kraft M, Leone F, Le-
toms, pulmonary function, and inflammatory markers. Curr manske RF, Martin RJ, Pesola GR, Peters SP, Sorkness CA,
Opin Pulm Med 2004;10:1–6. Szefler SJ, Israel E. Asthma Clinical Research Network,
11. Heany L. Severe asthma treatment: Need for characterising National Heart, Lung, and Blood Institute=NIH. Sputum
patients. Lancet 2005;365:974–976. eosinophil counts predict asthma control after discontinua-
12. Luskin A, Kosinski M, Breshahan B, Ashby M, Wong D. tion of inhaled corticosteroids. J Allergy Clin Immunol 2005;
Symptom control and improved functioning: The effect of 115:720–727.
omalizumab on asthma-related quality of life (ARQL). 31. Green R, Brightling C, McKenna S, Hargadon B, Parker D,
J Asthma 2005;42:823–827. Bradding P, Wardlaw AJ, Pavord ID. Asthma exacerbations
13. Zhang J, Yu C, Holgate S, Reiss T. Variability and lack of and sputum eosinophil counts: A randomised controlled
predictive ability of asthma end-points in clinical trials. Eur trial. Lancet 2002;360:1715–1721.
Respir J 2002;20:1102–1109. 32. Kim C, Hagan J. Sputum tests in the diagnosis and monitor-
14. D’Alonzo G, Steinijans V, Keller A. Measurement of morn- ing of asthma. Ann Allergy Asthma Immunol 2004;93:112–123.
ing and evening airflow grossly underestimate the circadian 33. Pizzichini E, Pizzichini M, Efthimiadis A, Dolovich J, Har-
variability of FEV1 and peak expiratory flow rate in asthma. greave F. Measuring airway inflammation in asthma: Eosi-
Am J Respir Crit Care Med 1995;152:1097–1099. nophils and eosinophilic cationic protein in induced sputum
15. Pino J, Garcia–Rio F, Prados C, Alvarez–Sala R, Diaz S, compared with peripheral blood. J Allergy Clin Immunol
Villasante C, Villamor J. Value of the peak expiratory flow 1997;99:539–544.
in bronchodynamic tests. Allergol Immunopathol 1996;34: 34. Nathan R, Sorkness C, Kosinski M, Schatz M, Li JT, Marcus
54–57. P, Murray JJ, Pendergraft TB. Development of the asthma
16. Moy M, Israel E, Weiss S, Juniper EF, Dube L, Drazen JM, control test: A survey for assessing asthma control. Clin
NHBLI Asthma Clinical Research Network. Clinical pre- Immunol 2004;113:59–65.
dictors of health-related quality of life depend on asthma 35. Schatz M, Sorkness CA, Li JT, Marcus P, Murray JJ, Nathan
severity. Am J Respir Crit Care Med 2001;163:924–929. RA, Kosinski M, Pendergraft TB, Jhingran P. Asthma control
17. Stahl E. Correlation between objective measures of airway test: Reliability, validity, and responsiveness in patients not
calibre and clinical symptoms in asthma: A systematic re- previously followed by asthma specialists. J Allergy Clin
view of clinical studies. Respir Med 2000;94:735–741. Immunol 2006;117:549–556.
18. Choi I, Koh Y, Lim H. Peak expiratory flow rate underesti- 36. Vollmer WM, Markson LE, O’Connor E, Sanocki LL, Fit-
mates severity of airflow obstruction in acute asthma. Korean terman L, Berger M, Bulst AS. Association of asthma control
J Intern Med 2002;17:174–179. with health care utilization and quality of life. Am J Respir
19. Cote J, Cartier A, Malo J–L, Rouleau M, Boulet L–P. Com- Crit Care Med 1999;160:1647–1652.
pliance with peak expiratory flow monitoring in home 37. Vollmer WM, Markson LE, O’Connor E, Frazier EA, Berger
management of asthma. Chest 1998;113:968–972. M, Bulst AS. Association of asthma control with health care
20. Currie G, Jackson C, Lipworth B. Does bronchial hyperre- utilization: A prospective evaluation. Am J Respir Crit Care
sponsiveness in asthma matter? J Asthma 2004;41:247–258. Med 2002;165:195–199.
21. Sterk P. Airway hyperresponsiveness: Using bronchial chal- 38. Peters D, Chen C, Markson L, Allen–Ramey F, Vollmer W.
lenge tests in research and management of asthma. J Aerosol Using an asthma questionnaire and administrative data to
Med 2002;15:123–129. predict health care utilization. Chest 2006;129:918–924.
22. O’Byrne P, Inman M. New considerations about measuring 39. Lieu T, Capra A, Quesenberry C, Mendoza G, Mazar M.
airway hyperresponsiveness. J Asthma 2000;37:293–302. Computer-based models to identify high-risk adults with
94 CARDARELLI

asthma: Is the glass half empty or half full? J Asthma 47. Eisner M, Ackerson L, Chi F, Kalkbrenner A, Buchner D,
1999;36:359–370. Mendoza G, Lieu I. Health-related quality of life and future
40. Juniper EF, O’Byrne PM, Guyatt GH, King DR. Develop- health care utilization for asthma. Ann Allergy Asthma Im-
ment and validation of a questionnaire to measure asthma munol 2002;89:46–55.
control. Eur Respir J 1999;14:902–907. 48. Juniper EF, Guyatt GH, Cox FM, Ferrie PJ, King, DR. De-
41. Juniper EF, O’Byrne PM, Ferrie PJ, King DR, Roberts JN. velopment and validation of the mini asthma quality of life
Measuring asthma control. Clinic questionnaire or daily di- questionnaire. Eur Respir J 1999;14:32–38.
ary? Am J Respir Crit Care Med 2000;162:1330–1334. 49. Bayliss MS, Espindle DM, Buchner d, Blaiss MS, Ware JE. A
42. Bateman E. Measuring asthma control. Curr Opin Allergy new tool for monitoring asthma outcomes, the ITG Asthma
Clin Immunol 2001;1:211–216. Short Form. Qual Life Res 2000;9:451–466.
43. Boulet L–P, Boulet V, Milot J. How should we quantify
asthma control? A proposal. Chest 2002;122:2217–2223.
44. Juniper E, Guyatt G, Ferrie P, Griffith L. Measuring quality Address reprints requests to:
of life in asthma. Am Rev Resp Dis 1993;147:832–838. William J. Cardarelli, R.Ph.
45. Juniper E, Buist A, Cox F, Ferrie P, King D. Validation of a Director of Pharmacy
standardized version of the Asthma Quality of Life Ques- Atrius Health=Harvard Vanguard Medical Associates
tionnaire. Chest 1999;115:1265–1270. 485 Arsenal Street
46. Juniper E, Guyatt G, Feeny D, Ferrie P, Griffith L, Townsend Watertown, MA 02472
M. Measuring quality of life in children with asthma. Qual
Life Res 1996;5:35–46. E-mail: William_Cardarelli@vmed.org

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