Asthma affects an estimated 7 million children and causes significant health care and disease burden. The most recent iteration of the National Heart, Lung and Blood Institute asthma guidelines, the Expert Panel Report 3, emphasizes the assessment and monitoring of asthma control in the management of asthma. Asthma control refers to the degree to which the manifestations of asthma are minimized by therapeutic interventions and the goals of therapy are met. Although assessment of asthma severity is used to guide initiation of therapy, monitoring of asthma control helps determine whether therapy should be maintained or adjusted. The nuances of estimation of asthma control include understanding concepts of current impairment and future risk and incorporating their measurement into clinical practice. Impairment is assessed on the basis of frequency and intensity of symptoms, variations in lung function, and limitations of daily activities. “Risk” refers to the likelihood of exacerbations, progressive loss of lung function, or adverse effects from medications. Currently available ambulatory tools to measure asthma control range are subjective measures, such as patient-reported composite asthma control score instruments or objective measures of lung function, airway hyperreactivity, and biomarkers. Because asthma control exhibits short- and long-term variability, health care providers need to be vigilant regarding the fluctuations in the factors that can create discordance between subjective and objective assessment of asthma control. Familiarity with the properties, application, and relative value of these measures will enable health care providers to choose the optimal set of measures that will adhere to national standards of care and ensure delivery of high-quality care customized to their patients.

Guidelines from the National Heart, Lung and Blood Institute for the diagnosis and management of asthma, and the Global Initiative for Asthma Control, revolve around the yardstick of evaluation of the severity of asthma and attainment of control to guide initiation and adjustment of therapy.1,2 Numerous studies have confirmed the inadequacy of asthma control in the United States.3,4 

The domains of severity and control can be assessed in terms of impairment (frequency and intensity of symptoms, variations in lung function, and limitations of daily activities) and future risk (likelihood of exacerbations, progressive loss of lung function, or adverse effects from medications). Asthma can be considered to be well controlled if symptoms are present twice a week or less; rescue bronchodilator medication is used twice a week or less; there is no nocturnal or early awakening; there are no limitations of work, school, or exercise; and the peak flow (PEF)/forced expiratory volume in 1 second (FEV1) is normal or at the personal best. Asthma control can be further classified as well controlled, not well controlled, and very poorly controlled as elegantly laid out in the National Heart, Lung and Blood Institute Expert Panel Report 3 (EPR3).1 Asthma can be considered not well controlled if symptoms are present more than 2 days a week or multiple times on 2 or fewer days per week; rescue bronchodilator medication is used more than 2 days per week; nighttime awakenings are 2 times a month or more; there is some limitation of work, school, or exercise; and the PEF/FEV1 is 60% to 80% of personal best/predicted, respectively. Asthma is classified as very poorly controlled if symptoms are present throughout the day; rescue bronchodilator medication is used several times per day; nighttime awakenings are more than 1 time a week; there is extreme limitation of work, school, or exercise; and the PEF/FEV1 is less than 60% of personal best/predicted, respectively.

The keystone of asthma management is the achievement and maintenance of optimal asthma control. However, to date, there is no universally recognized gold standard measure of asthma control that can accurately capture both patient-reported domains of impairment and risk and objective measures of lung function. The tools available in a clinical practice setting can be classified as subjective (“patient reported”) and objective (“physiologic and inflammatory measures”). A judicious combination of measures from each category may be needed to optimally assess asthma control.

Subjective measures of asthma control include (1) detailed history taking, (2) use of composite asthma control scores, and (3) quality-of-life measures (used mainly in research settings).

Assessment of asthma control in the health care provider’s office starts with the history. Detailed information should be sought on patient-centered outcomes (such as asthma exacerbations in the past year and the limitations asthma imposes on the patient’s daily activities including sports and play), sleep disturbance, medication use (both daily controller and reliever medication), adherence to therapy, and comorbidities/factors that may complicate care.5 

Patient-reported composite asthma control score instruments are attempts to capture the multidimensional nature of asthma control in a single numerical value. This enables the degree of asthma control to be compared across encounters. More than 17 composite instruments, each with at least 1 published validated study, are available.6 These instruments have comparable content and have been designed to measure asthma disease activity over a period of 1 to 4 weeks. Notably, none of them have been validated to assess an acute exacerbation (Table 1). Therefore, from a pediatric emergency medicine perspective, caution should be taken when using composite asthma score instruments during an acute exacerbation, as is typically encountered in the emergency department setting.

TABLE 1

Age-Specific Asthma Control Tools and Their Properties

AgeInstrument
0–4 y TRACK 
5–11 y/older children Asthma Quiz, ATAQ for Children and Adolescents, Breathmobile Assessment of Asthma Control, Asthma Control in Children, Functional Severity of Asthma Scale, C-ACT, and Pediatric Asthma Control Tool 
12 y and older ACT and ACQ 
18 y and older Asthma Control and Communication Instrument, ATAQ, Seattle Asthma Severity and Control Questionnaire, and 30-Second Asthma Test 
Comments Other asthma questionnaires include the Asthma Quiz for Kidz, the 23-item/13-item Pediatric Asthma Quality of Life Questionnaire (PAQLQ)/Mini-PAQLQ, the Pediatric Quality of Life Inventory, the Asthma Routines Questionnaire, and the Pediatric Asthma Control and Communication Instrument 
Tool Properties 
ACT (5-item questionnaire) Composite, numeric score (up to 25) 
 MCID 3 points 
 Controlled >19 
 Poorly controlled ≤15 
C-ACT (7-item questionnaire) 4 filled out by child, 3 questions by parent/caregiver 
 Composite numeric score (up to 27) 
 MCID 2 points 
 Controlled >19 
ACQ (7 items: 6 questionnaire, and 1 FEV1Composite numeric score (up to 6) 
 MCID 0.5 points 
 Controlled >19 
ATAQ (4-item questionnaire in the control dimension; overall 20 questions) Composite numeric score (up to 4) 
 MCID: none established 
 Controlled (0); not well controlled (1–2), poorly controlled (3–4) 
TRACK (5-item questionnaire) Composite numeric score (up to 100) 
 MCID: 10 
 Controlled (≥80) 
AgeInstrument
0–4 y TRACK 
5–11 y/older children Asthma Quiz, ATAQ for Children and Adolescents, Breathmobile Assessment of Asthma Control, Asthma Control in Children, Functional Severity of Asthma Scale, C-ACT, and Pediatric Asthma Control Tool 
12 y and older ACT and ACQ 
18 y and older Asthma Control and Communication Instrument, ATAQ, Seattle Asthma Severity and Control Questionnaire, and 30-Second Asthma Test 
Comments Other asthma questionnaires include the Asthma Quiz for Kidz, the 23-item/13-item Pediatric Asthma Quality of Life Questionnaire (PAQLQ)/Mini-PAQLQ, the Pediatric Quality of Life Inventory, the Asthma Routines Questionnaire, and the Pediatric Asthma Control and Communication Instrument 
Tool Properties 
ACT (5-item questionnaire) Composite, numeric score (up to 25) 
 MCID 3 points 
 Controlled >19 
 Poorly controlled ≤15 
C-ACT (7-item questionnaire) 4 filled out by child, 3 questions by parent/caregiver 
 Composite numeric score (up to 27) 
 MCID 2 points 
 Controlled >19 
ACQ (7 items: 6 questionnaire, and 1 FEV1Composite numeric score (up to 6) 
 MCID 0.5 points 
 Controlled >19 
ATAQ (4-item questionnaire in the control dimension; overall 20 questions) Composite numeric score (up to 4) 
 MCID: none established 
 Controlled (0); not well controlled (1–2), poorly controlled (3–4) 
TRACK (5-item questionnaire) Composite numeric score (up to 100) 
 MCID: 10 
 Controlled (≥80) 

Adapted from Cloutier et al.6 MCID, minimally clinically important difference.

The commonly used validated tools are the Asthma Control Test (ACT),7 the Childhood Asthma Control Test C-ACT,8 and the Asthma Control Questionnaire (ACQ).9 The ACT contains 5 items, with a recall window of 4 weeks. The C-ACT is for use in children 4 through 11 years of age and consists of 4 pictorial items and 3 verbal items that are scored by the children and parents, respectively. It has been reported that children tend to assess their asthma control to be significantly lower than their parents do. The Asthma Control Questionnaire (ACQ) contains 6 items with a recall window of 1 week, supplemented by percentage of predicted FEV1 measurement. The Test for Respiratory and Asthma Control in Kids (TRACK)10 is a 5-question caregiver-completed questionnaire that determines respiratory control in children 0 to 5 years of age with symptoms consistent with asthma. Another less commonly used instrument is the Asthma Therapy Assessment Questionnaire (ATAQ), a 20-item parent-completed questionnaire exploring several domains, with 4 questions relating to symptom control and primarily used in research.11,12 

Individual instruments contain 3 to 10 questions, and scoring varies by instrument (Table 1). Four instruments have established cutoff values for uncontrolled versus controlled asthma (ACQ, ACT, C-ACT, and TRACK), and 2 have cutoffs for identifying poorly controlled asthma (ACT and ATAQ). Because these cutoffs have been defined at a population level, they may not be accurate for an individual patient. Tracking the numerical and categorical responses over time for each individual patient may prove to be more helpful than looking at cutoff values alone. For instance, if a patient reports frequent nocturnal awakenings, following the response to that particular question may help individualize attainment of control. The minimal clinically important differences or temporal differences in scores that indicate clinical significance have been determined for a few of the instruments (ACQ, ACT, C-ACT, and TRACK6,13; Table 1). Three of the instruments (ACQ, ACT, and TRACK) have been validated in Spanish-speaking groups.14,16 The ACQ and ACT have been validated for use as self-administered instruments in person, at home, by telephone, and by Internet tracking.6,17 

Poor asthma control, as measured by the commonly used composite scores, is associated with reduced lung function and elevated exhaled nitric oxide fraction5,18 (discussed later in the article). Studies have shown that changes in these composite scores reflect changes in the overall clinical assessment of asthma control by physicians and the need to step-up therapy.19 However, a recent study showed that the degree of asthma control, as assessed by these tools, changes over time and shows variable concordance with the risk of exacerbations.12 

Despite being fairly well validated, these scores share drawbacks that limit their usefulness in clinical practice.6 Although the short recall window facilitates reliable recollection of recent asthma events, it fails to represent the fluctuations in control. Children may be excellently controlled during one season and then have poor control during another. In addition, asthma exacerbations can occur in children with good short-term asthma control.20 Exacerbations, an important component of the impairment domain of asthma control, are not covered in the ACT, C-ACT, and ACQ but are assessed in the TRACK and the Composite Asthma Severity Index.21,22 

A range of pediatric asthma quality-of-life instruments have been developed, encompassing the impact of asthma on children’s or their parents’ lives.23 The instruments have been validated but are time-intensive to fill out and are therefore not routinely used in clinical practice.

Currently available objective measures of asthma control include (1) assessment of lung function, (2) evaluation of airway hyperresponsiveness, and (3) biomarkers.

Peak Flow

The PEF is defined as the highest instantaneous expiratory flow achieved during a maximal forced expiratory maneuver starting at total lung capacity.24 PEF variability is the degree to which the PEF varies among multiple measurements performed over time (Table 2). The management of acute exacerbations has traditionally been guided by PEF measurements. However, the correlation between PEF and FEV1 worsens in asthmatic patients with airflow limitation. Also, although reference to normal PEF values is important, the “personal best” value, and the trend of change in individual patients, is of greater value in managing their asthma.24 

TABLE 2

Objective Measures of Asthma Control

Spirometry Measured by ATS/ERS guidelines and using NHANES-3 normative values. Serial measures should be performed at the same time each day, if possible (Indicate whether bronchodilator was withheld before test.) 
 Standardized methodology and equipment (ATS/ERS guidelines) 
 Performed in a clinic/laboratory setting under the supervision of a qualified technician 
 Can be performed by children >5 y (in general) under guidance of trained personnel 
 Portable and handheld devices available for use in the field/home settings 
 FEV1 report: 
  Percent predicted values (at baseline and at any other time point, if applicable) 
  Changes over the course of evaluation: 
   Percent change from baseline in the absolute value 
   Absolute change from baseline (in milliliters) 
   Change from baseline in the percent predicted value 
 FEV1/FVC report: 
  Ratio of absolute values (at baseline and at any other time point, if applicable) 
  Changes over the course of evaluation: 
   Absolute change from baseline in the value of the ratio 
   Change from baseline in the percent predicted value 
Bronchodilator reversibility (prebronchodilator and postbronchodilator spirometry) 1. Withhold bronchodilator before the measure (12–24 h for long-acting β-2-agonists or anticholinergics; 4–6 h for short-acting β-agonists) 
 2. Administer 4 separate puffs of albuterol (90 mg of albuterol base/puff) with spacer at 30-s intervals between puffs, followed by spirometry after 15 min 
 Report: 
  Prebronchodilator and postbronchodilator FEV1 (expressed as percent predicted) 
  Percent change from prebronchodilator to postbronchodilator in the absolute value of FEV1 
  Absolute change in FEV1 from prebronchodilator to postbronchodilator (in milliliters) 
PEF PEF is a measure of maximum instantaneous expiratory 
 Can be self-administered on a daily basis and results recorded manually or electronically to obtain day-to-day or within-day variability 
 Percent predicted values (NHANES-3 normative values) 
 When measured with a peak flowmeter, PEF is usually expressed in units of L/min; in contrast, when PEF is measured with spirometry systems, it is usually expressed in units of liters/second 
 Percent change from baseline in the absolute values over the course of evaluation 
 Absolute change from baseline over the course of the evaluation (in liters/minute) 
 Variability (diurnal amplitude as a percentage of the day’s mean) 
Spirometry Measured by ATS/ERS guidelines and using NHANES-3 normative values. Serial measures should be performed at the same time each day, if possible (Indicate whether bronchodilator was withheld before test.) 
 Standardized methodology and equipment (ATS/ERS guidelines) 
 Performed in a clinic/laboratory setting under the supervision of a qualified technician 
 Can be performed by children >5 y (in general) under guidance of trained personnel 
 Portable and handheld devices available for use in the field/home settings 
 FEV1 report: 
  Percent predicted values (at baseline and at any other time point, if applicable) 
  Changes over the course of evaluation: 
   Percent change from baseline in the absolute value 
   Absolute change from baseline (in milliliters) 
   Change from baseline in the percent predicted value 
 FEV1/FVC report: 
  Ratio of absolute values (at baseline and at any other time point, if applicable) 
  Changes over the course of evaluation: 
   Absolute change from baseline in the value of the ratio 
   Change from baseline in the percent predicted value 
Bronchodilator reversibility (prebronchodilator and postbronchodilator spirometry) 1. Withhold bronchodilator before the measure (12–24 h for long-acting β-2-agonists or anticholinergics; 4–6 h for short-acting β-agonists) 
 2. Administer 4 separate puffs of albuterol (90 mg of albuterol base/puff) with spacer at 30-s intervals between puffs, followed by spirometry after 15 min 
 Report: 
  Prebronchodilator and postbronchodilator FEV1 (expressed as percent predicted) 
  Percent change from prebronchodilator to postbronchodilator in the absolute value of FEV1 
  Absolute change in FEV1 from prebronchodilator to postbronchodilator (in milliliters) 
PEF PEF is a measure of maximum instantaneous expiratory 
 Can be self-administered on a daily basis and results recorded manually or electronically to obtain day-to-day or within-day variability 
 Percent predicted values (NHANES-3 normative values) 
 When measured with a peak flowmeter, PEF is usually expressed in units of L/min; in contrast, when PEF is measured with spirometry systems, it is usually expressed in units of liters/second 
 Percent change from baseline in the absolute values over the course of evaluation 
 Absolute change from baseline over the course of the evaluation (in liters/minute) 
 Variability (diurnal amplitude as a percentage of the day’s mean) 

Adapted from Tepper et al.24 

The advantages of PEF are that it is easier to perform than a spirometric maneuver and it is measurable with a relatively small and inexpensive instrument. Thus, PEF may be suitable for individual testing at home, at school, and in patients who are poor perceivers of their degree of airway obstruction. It may help prevent delayed treatment in underperceivers and excessive use of services in overperceivers.

Many concerns regarding PEF have been described, with the primary ones being that the results are highly variable even when performed well, limiting its utility in the diagnosis and management of asthma. Parents and child should be appropriately trained on use, but there is no gauge of effort, and it gives no information regarding the site of airflow obstruction. It cannot distinguish obstructive from restrictive ventilatory impairment. PEF meters from different manufacturers may show different results, and the “personal best” measurements may change with growth and degree of asthma control. Adherence to PEF monitoring is a challenge25 and is often the reason it is not widely used in clinical practice. Overall, PEF monitoring alone has not been shown to be more effective than symptom monitoring on influencing asthma outcomes26 and is no longer recommended.1 

Spirometry

Measurement of spirometric indices of lung function, such as the FEV1, forced vital capacity (FVC), and FEV1/FVC ratio, are an integral part of the assessment of asthma severity, control, and response to treatment.1,2 They have been shown to be associated with the risk of asthma attacks in children.27 Children with chronic airway obstruction have been reported to be less likely to perceive dyspnea than those with acute obstruction.28 The EPR3, therefore, recommends performing office-based spirometry every 1 to 2 years and more frequently if clinically indicated in children 5 years or older with asthma.1 However, only 20% to 40% of primary care providers use lung function measurements in asymptomatic asthmatic patients, and up to 59% of pediatricians never perform lung function tests.29 

Normal values for spirometry are well established and are based on height, age, sex, and race/ethnicity of the healthy US population. Spirometric measures are highly reproducible within testing sessions in approximately 75% of children older than 5 to 6 years of age. Guidance on performing spirometry in an office setting and coding for asthma visits have been described.30 The forced expiratory maneuver may be displayed as a flow-volume loop. Guidelines regarding interpretation of the primary measures (FEV1, FVC, and the FEV1/FVC ratio) are well outlined in the EPR3.1,31 Of note, most automatic interpretations of the spirometry report fail to comment on the FEV1/FVC ratio, an important parameter that, in children, is normally 85% predicted or greater.1 Forced expiratory flow between 25% and 75% of vital capacity (FEF25–75) may reflect obstructive changes that occur in the small airways of children with asthma. However, FEF25–75 is considered to be of secondary importance because it is not specific and is highly variable (effort dependent).

Reduced spirometric measures are associated with symptom severity, reduced quality of life, and poor asthma outcomes.24 However, individual patients, particularly children, may have misleadingly normal spirometry results, despite frequent or severe symptoms. An analysis of 2728 children between 4 and 18 years of age attending a tertiary care facility showed that the majority of asthmatic children had FEV1 values within normal ranges.32 

Spirometry, by itself, is not useful in establishing the diagnosis of asthma because airflow limitation may be mild or absent, particularly in children. In other words, if the spirometry result is normal, it does not rule out asthma. Variability of airflow obstruction over time and the response to treatment, when clinically relevant, can aid in the diagnosis and assessment of asthma control.

Although there are organizations that are attempting to integrate spirometry results into the electronic health record with varying degrees of success, the most commonly used approach at this time is to scan the printed spirometry result into the electronic health record.

Prebronchodilator and Postbronchodilator Spirometry (Bronchodilator Reversibility)

Bronchodilator reversibility testing helps determine the presence and magnitude of reversible airflow limitation.24 Baseline spirometry is performed and repeated after administration of bronchodilator test agents (eg, 15 minutes after 4 inhalations of albuterol). Change in FEV1 is the most common parameter followed because the value of reversibility in other measurements is less established (eg, FEV1/FVC or FEF25–75).

The most widely used definition of “significant” bronchodilator response is that of the American Thoracic Society/European Respiratory Society (ATS/ERS) guidelines for interpretation of spirometry and consists of an improvement in FEV1 greater than 12% and 200 mL.33 Other parameters that have been used in children include a 9% to 10% increase in percent predicted FEV1.24 

Bronchodilator reversibility testing, although not specific, is useful for confirming the diagnosis of asthma. Increased bronchodilator reversibility correlates with increased asthma severity. Bronchodilator reversibility is diminished in patients with well-controlled asthma as well as those with narrowing or remodeling of the airways. Annual assessment of prebronchodilator and postbronchodilator FEV1 might help identify children at risk for developing progressive decline in airflow.34 

Recent Advances in Monitoring PEF and Spirometry

Advances in home-based airflow monitoring include the use of electronic, handheld devices with easily downloadable recordings of multiple PEF or FEV1 point measures with software that facilitates easy use and interpretation.35 The availability of these instruments for routine clinical use is limited at this time.

Impulse Oscillometry

Impulse oscillometry assesses airflow resistance and bronchodilator response in younger children. Measurement of airway resistance is a direct indicator of airway caliber with increased resistance indicating narrowing of airways. It is used largely as a research tool and is only available in a few centers.24 

A major characteristic of asthma is the variability in bronchial tone in response to a variety of stimuli. Airway hyperresponsiveness (AHR) may be assessed by bronchial provocation tests. Bronchial provocation tests may be performed with agents such as methacholine or stimuli such as physical exercise.24,28,36 A positive test result for AHR is indicated by a 20% reduction in FEV1 after inhalation of a methacholine dose of 8 mg/mL or less. A negative test suggests a diagnosis other than asthma. A reduction in FEV1 of at least 10% during exercise testing is taken as a sign of exercise-induced bronchoconstriction. These tests take approximately 2 hours and require trained personnel to perform them. In general, evidence does not support the routine assessment of AHR in the clinical management of asthma control.28 

Apart from exhaled nitric oxide measurements, the role and usefulness of noninvasive biomarkers in routine clinical practice for monitoring inflammation in children with asthma is undefined. Sputum eosinophilia, exhaled breath condensates, and urinary leukotrienes are used as tools primarily in research studies.28,37 

Exhaled Nitric Oxide

The fractional concentration of nitric oxide in exhaled air (FENO) is a quantitative measure of airway nitric oxide, an endogenously produced gaseous mediator that is an indirect marker of airway inflammation. The joint ATS/ERS guideline for the measurement of FENO is the current standard.38,39 The testing is noninvasive, reproducible, easy to perform in patients (including children), feasible to measure in ambulatory clinical settings, and has no risk to patients.40,41 

FENO is generally accepted as a marker of eosinophilic airway inflammation. Individuals with asthma have been reported to have elevated levels of FENO, but because FENO is also related to atopy, elevated levels may be seen in atopic individuals without asthma. Although FENO levels overlap among healthy, atopic, and asthmatic cohorts, in general, the upper value of normal is 25 ppb. It has been suggested that a clinically important decrease of FENO is a change of 20% for values greater than 50 ppb or a change of 10 ppb for values less than 50 ppb.38 Studies in children suggest that FENO correlates with severity and with asthma control.42 FENO reduces in a dose-dependent manner with corticosteroid treatment43 and has been shown to increase with deterioration in asthma control.44 The value of additional FENO monitoring in children whose asthma is appropriately managed using guideline-based strategies is unproven,28,45,47 and insurance payment for this test varies by geographic location. Nevertheless, some asthma specialists have adopted the use of FENO as an adjunct ambulatory clinical tool for measuring airway inflammation and serial monitoring asthma control in individual patients with difficult-to-control asthma.

Assessing Asthma Control in Children Younger Than 5 Years

In children younger than 5 years, it is recommended that both symptom control and future risk be monitored.2 The risk domain is assessed by historical review of exacerbations with need for oral steroid. Validated measures to assess asthma control in this age group include the TRACK (0–5 years) and the C-ACT in children (4–11 years) of age.

Children younger than 5 years are typically unable to perform spirometry; hence, confirmation of the diagnosis of asthma is challenging in this age group. Recurrent wheezing occurs in a large proportion of these children, typically with viral infections. A therapeutic trial of regular controller therapy (for 1–3 months) may often be necessary to evaluate response and maintenance of control.

Assessment of risk profiles using tools such as the asthma predictive index (API) may be helpful in predicting the likelihood of recurrent wheezing in school-age children. One study showed that children with a positive API had a fourfold to 10-fold greater chance of developing asthma at 6 through 13 years of age than those with a negative API, and 95% of children with a negative API remained free of asthma.48 The modified API suggests that the diagnosis of asthma in young children with a history of more than 3 episodes of wheezing is more likely if they meet 1 major or 2 minor criteria.49 Major criteria include a parent with asthma, physician diagnosis of atopic dermatitis, or sensitization to aeroallergens (positive skin or allergen-specific immunoglobulin E test results). Minor criteria include the presence of food allergies or sensitization to milk, egg, and peanut; blood eosinophil counts greater than 4%; or wheezing apart from colds.49 

Recent advances in measuring lung function, biomarker profiles, adherence, utilization and outcomes data, and development of validated questionnaires have made ongoing assessment and monitoring of asthma control a reality. Following is a schema of suggested measures that may be used in routine ambulatory monitoring of asthma control in clinical practice.

  • The encounter between patient and health care provider may involve critical and empathetic listening to the patient and accurate elicitation of symptoms as indicators for asthma control, aided by validated asthma control tools such as the C-ACT/ACT. A complete environmental and social history should be obtained to evaluate for triggers.50 

  • Airway obstruction and AHR can be assessed by measuring prebronchodilator and postbronchodilator FEV1. Some specialists may consider evaluation of airway inflammation by using FENO to be useful.

  • Education and training regarding asthma and its management can be provided, taking into consideration the patient’s personal preference and goals while creating an individualized action plan.

  • Action strategies can be based on either symptoms or objective criteria, such as by monthly monitoring of the age-specific, validated asthma control instrument, or in individualized circumstances, by daily electronic FEV1 or conventional peak flow monitoring at home.

  • Symptom scores with validated control instruments and FEV1 can be monitored at subsequent visits along with serial health care utilization data to tailor the medication dose to degree of asthma control. The risk domain is validated by a history of systemic steroid prescription, emergency department visits, or hospitalizations.

  • In individuals whose FENO was elevated at the initial visit and shows variation in response to therapy, repeat FENO monitoring may be considered.

  • Education regarding asthma triggers, review of inhaler techniques, assessment and reinforcement of adherence, treatment of comorbidities (eg, gastroesophageal reflux, sinusitis, obesity), and encouragement and fortification of the collaborative provider-patient relationship can be provided at each follow-up visit.

  • The need for continued assessment or reassessment by a pediatric allergist or pulmonologist can be considered when faced with challenges in attaining optimal asthma control.

  • Information on appropriate coding for the asthma management tools and services provided can be found in the Asthma Coding Fact Sheet at the following link: https://www.aap.org/asthmacodingfactsheets.

ACT

Asthma Control Test

ACQ

Asthma Control Questionnaire

AHR

airway hyperresponsiveness

ATAQ

Asthma Therapy Assessment Questionnaire

ATS/ERS

American Thoracic Society/European Respiratory Society

C-ACT

Childhood Asthma Control

EPR3

Expert Panel Report 3

FENO

fractional exhaled nitric oxide

FEV1

forced expiratory volume in 1 second

FEF25–75

forced expiratory flow between 25% and 75% of vital capacity

FEV1/FVC ratio

ratio of forced expiratory volume in 1 second to forced expiratory volume

FVC

forced expiratory volume

PEF

peak flow

TRACK

Test for Respiratory and Asthma Control in Kids

FUNDING: No external funding.

This document is copyrighted and is property of the American Academy of Pediatrics and its Board of Directors. All authors have filed conflict of interest statements with the American Academy of Pediatrics. Any conflicts have been resolved through a process approved by the Board of Directors. The American Academy of Pediatrics has neither solicited nor accepted any commercial involvement in the development of the content of this publication.

Clinical reports from the American Academy of Pediatrics benefit from expertise and resources of liaisons and internal (AAP) and external reviewers. However, clinical reports from the American Academy of Pediatrics may not reflect the views of the liaisons or the organizations or government agencies that they represent.

The guidance in this report does not indicate an exclusive course of treatment or serve as a standard of medical care. Variations, taking into account individual circumstances, may be appropriate.

All clinical reports from the American Academy of Pediatrics automatically expire 5 years after publication unless reaffirmed, revised, or retired at or before that time.

1
National Asthma Education and Prevention Program
.
Expert Panel Report 3 (EPR-3). Guidelines for the diagnosis and management of asthma—summary report 2007.
J Allergy Clin Immunol
.
2007
;
120
(
s
uppl
5
):
S94
S138
[PubMed]
2
Global Strategy for Asthma Management and Prevention, Global Initiative for Asthma (GINA) 2015 Update
.
2015
. Available at: www.ginasthma.org. Accessed June 14, 2016
3
Fuhlbrigge
AL
,
Adams
RJ
,
Guilbert
TW
, et al
.
The burden of asthma in the United States: level and distribution are dependent on interpretation of the national asthma education and prevention program guidelines.
Am J Respir Crit Care Med
.
2002
;
166
(
8
):
1044
1049
[PubMed]
4
Carlton
BG
,
Lucas
DO
,
Ellis
EF
,
Conboy-Ellis
K
,
Shoheiber
O
,
Stempel
DA
.
The status of asthma control and asthma prescribing practices in the United States: results of a large prospective asthma control survey of primary care practices.
J Asthma
.
2005
;
42
(
7
):
529
535
[PubMed]
5
Brand
PL
,
Mäkelä
MJ
,
Szefler
SJ
,
Frischer
T
,
Price
D
;
ERS Task Force Monitoring Asthma in Children
.
Monitoring asthma in childhood: symptoms, exacerbations and quality of life.
Eur Respir Rev
.
2015
;
24
(
136
):
187
193
[PubMed]
6
Cloutier
MM
,
Schatz
M
,
Castro
M
, et al
.
Asthma outcomes: composite scores of asthma control.
J Allergy Clin Immunol
.
2012
;
129
(
3
Suppl
):
S24
S33
[PubMed]
7
Nathan
RA
,
Sorkness
CA
,
Kosinski
M
, et al
.
Development of the asthma control test: a survey for assessing asthma control.
J Allergy Clin Immunol
.
2004
;
113
(
1
):
59
65
[PubMed]
8
Liu
AH
,
Zeiger
RS
,
Sorkness
CA
, et al
The Childhood Asthma Control Test: retrospective determination and clinical validation of a cut point to identify children with very poorly controlled asthma.
J Allergy Clin Immunol
.
2010
;
126
(
2
):
267
273
,
273.e1
9
Juniper
EF
,
Gruffydd-Jones
K
,
Ward
S
,
Svensson
K
.
Asthma Control Questionnaire in children: validation, measurement properties, interpretation.
Eur Respir J
.
2010
;
36
(
6
):
1410
1416
[PubMed]
10
Chipps
B
,
Zeiger
RS
,
Murphy
K
, et al
.
Longitudinal validation of the Test for Respiratory and Asthma Control in Kids in pediatric practices.
Pediatrics
.
2011
;
127
(
3
):
e737
e747
[PubMed]
11
Skinner
EA
,
Diette
GB
,
Algatt-Bergstrom
PJ
, et al
.
The Asthma Therapy Assessment Questionnaire (ATAQ) for children and adolescents.
Dis Manag
.
2004
;
7
(
4
):
305
313
[PubMed]
12
Wu
AC
,
Tantisira
K
,
Li
L
,
Schuemann
B
,
Weiss
ST
,
Fuhlbrigge
AL
;
Childhood Asthma Management Program Research Group
.
Predictors of symptoms are different from predictors of severe exacerbations from asthma in children.
Chest
.
2011
;
140
(
1
):
100
107
[PubMed]
13
Schatz
M
,
Kosinski
M
,
Yarlas
AS
,
Hanlon
J
,
Watson
ME
,
Jhingran
P
.
The minimally important difference of the Asthma Control Test.
J Allergy Clin Immunol
.
2009
;
124
(
4
):
719
-
23.e1
14
Okelo
SO
,
Eakin
MN
,
Patino
CM
, et al
.
The Pediatric Asthma Control and Communication Instrument asthma questionnaire: for use in diverse children of all ages.
J Allergy Clin Immunol
.
2013
;
132
(
1
):
55
62
[PubMed]
15
Picado
C
,
Badiola
C
,
Perulero
N
, et al;
Covalair Investigator Group
.
Validation of the Spanish version of the Asthma Control Questionnaire.
Clin Ther
.
2008
;
30
(
10
):
1918
1931
[PubMed]
16
Rodrigo
GJ
,
Arcos
JP
,
Nannini
LJ
, et al
.
Reliability and factor analysis of the Spanish version of the asthma control test.
Ann Allergy Asthma Immunol
.
2008
;
100
(
1
):
17
22
[PubMed]
17
Schatz
M
,
Sorkness
CA
,
Li
JT
, et al
.
Asthma Control Test: reliability, validity, and responsiveness in patients not previously followed by asthma specialists.
J Allergy Clin Immunol
.
2006
;
117
(
3
):
549
556
[PubMed]
18
Piacentini
GL
,
Peroni
DG
,
Bodini
A
, et al
.
Childhood Asthma Control Test and airway inflammation evaluation in asthmatic children.
Allergy
.
2009
;
64
(
12
):
1753
1757
[PubMed]
19
Chipps
BE
,
Zeiger
RS
,
Dorenbaum
A
, et al;
TENOR Study Group
.
Assessment of asthma control and asthma exacerbations in the epidemiology and natural history of asthma: outcomes and treatment regimens (TENOR) observational cohort.
Curr Respir Care Rep
.
2012
;
1
(
4
):
259
269
[PubMed]
20
Jackson
DJ
,
Sykes
A
,
Mallia
P
,
Johnston
SL
.
Asthma exacerbations: origin, effect, and prevention.
J Allergy Clin Immunol
.
2011
;
128
(
6
):
1165
1174
[PubMed]
21
Chipps
BE
,
Mellon
MM
,
Murphy
KR
,
Zeiger
RS
.
Test for respiratory and asthma control in kids (TRACK): a validated control tool for preschool-aged children.
J Allergy Clin Immunol
.
2014
;
133
(
6
):
1776
[PubMed]
22
Wildfire
JJ
,
Gergen
PJ
,
Sorkness
CA
, et al
.
Development and validation of the Composite Asthma Severity Index—an outcome measure for use in children and adolescents.
J Allergy Clin Immunol
.
2012
;
129
(
3
):
694
701
[PubMed]
23
Wilson
SR
,
Rand
CS
,
Cabana
MD
, et al
.
Asthma outcomes: quality of life.
J Allergy Clin Immunol
.
2012
;
129
(
s
uppl
3
):
S88
S123
[PubMed]
24
Tepper
RS
,
Wise
RS
,
Covar
R
, et al
.
Asthma outcomes: pulmonary physiology.
J Allergy Clin Immunol
.
2012
;
129
(
s
uppl
3
):
S65
S87
[PubMed]
25
Kamps
AW
,
Roorda
RJ
,
Brand
PL
.
Peak flow diaries in childhood asthma are unreliable.
Thorax
.
2001
;
56
(
3
):
180
182
[PubMed]
26
Gibson
PG
.
Monitoring the patient with asthma: an evidence-based approach.
J Allergy Clin Immunol
.
2000
;
106
(
1 pt 1
):
17
26
[PubMed]
27
Fuhlbrigge
AL
,
Kitch
BT
,
Paltiel
AD
, et al
.
FEV(1) is associated with risk of asthma attacks in a pediatric population.
J Allergy Clin Immunol
.
2001
;
107
(
1
):
61
67
[PubMed]
28
Moeller
A
,
Carlsen
KH
,
Sly
PD
, et al;
ERS Task Force Monitoring Asthma in Children
.
Monitoring asthma in childhood: lung function, bronchial responsiveness and inflammation.
Eur Respir Rev
.
2015
;
24
(
136
):
204
215
[PubMed]
29
Dombkowski
KJ
,
Hassan
F
,
Wasilevich
EA
,
Clark
SJ
.
Spirometry use among pediatric primary care physicians.
Pediatrics
.
2010
;
126
(
4
):
682
687
[PubMed]
30
American Academy of Pediatrics
. Coding fact sheets and billing position papers. Available at: www.aap.org/asthmacodingfactsheets. Accessed December 23, 2015
31
Spahn
JD
,
Chipps
BE
.
Office-based objective measures in childhood asthma.
J Pediatr
.
2006
;
148
(
1
):
11
15
[PubMed]
32
Paull
K
,
Covar
R
,
Jain
N
,
Gelfand
EW
,
Spahn
JD
.
Do NHLBI lung function criteria apply to children? A cross-sectional evaluation of childhood asthma at National Jewish Medical and Research Center, 1999–2002.
Pediatr Pulmonol
.
2005
;
39
(
4
):
311
317
[PubMed]
33
Miller
MR
,
Hankinson
J
,
Brusasco
V
, et al;
ATS/ERS Task Force
.
Standardisation of spirometry.
Eur Respir J
.
2005
;
26
(
2
):
319
338
[PubMed]
34
Horak
E
,
Lanigan
A
,
Roberts
M
, et al
.
Longitudinal study of childhood wheezy bronchitis and asthma: outcome at age 42.
BMJ
.
2003
;
326
(
7386
):
422
423
[PubMed]
35
Vilozni
D
,
Barak
A
,
Efrati
O
, et al
.
The role of computer games in measuring spirometry in healthy and “asthmatic” preschool children.
Chest
.
2005
;
128
(
3
):
1146
1155
[PubMed]
36
Crapo
RO
,
Casaburi
R
,
Coates
AL
, et al
.
Guidelines for methacholine and exercise challenge testing-1999. This official statement of the American Thoracic Society was adopted by the ATS Board of Directors, July 1999.
Am J Respir Crit Care Med
.
2000
;
161
(
1
):
309
329
[PubMed]
37
Szefler
SJ
,
Wenzel
S
,
Brown
R
, et al
.
Asthma outcomes: biomarkers.
J Allergy Clin Immunol
.
2012
;
129
(
s
uppl
3
):
S9
S23
[PubMed]
38
Dweik
RA
,
Boggs
PB
,
Erzurum
SC
, et al;
American Thoracic Society Committee on Interpretation of Exhaled Nitric Oxide Levels (FENO) for Clinical Applications
.
An official ATS clinical practice guideline: interpretation of exhaled nitric oxide levels (FENO) for clinical applications.
Am J Respir Crit Care Med
.
2011
;
184
(
5
):
602
615
[PubMed]
39
AAAAI/ACAAI Joint Statement of Support of the ATS Clinical Practice Guideline
. Interpretation of Exhaled Nitric Oxide for Clinical Applications. Available at: www.aaaai.org/Aaaai/media/MediaLibrary/PDF%20Documents/My%20Membership/FeNOJointStatement3-6-12.pdf. Accessed June 14, 2016
40
Dinakar
C
.
Exhaled nitric oxide in asthma management.
Ann Allergy Asthma Immunol
.
2012
;
108
(
4
):
219
222
[PubMed]
41
Hanson
JR
,
De Lurgio
SA
,
Williams
DD
,
Dinakar
C
.
Office-based exhaled nitric oxide measurement in children 4 years of age and older.
Ann Allergy Asthma Immunol
.
2013
;
111
(
5
):
358
363
[PubMed]
42
Delgado-Corcoran
C
,
Kissoon
N
,
Murphy
SP
,
Duckworth
LJ
.
Exhaled nitric oxide reflects asthma severity and asthma control.
Pediatr Crit Care Med
.
2004
;
5
(
1
):
48
52
[PubMed]
43
Kharitonov
SA
,
Donnelly
LE
,
Montuschi
P
,
Corradi
M
,
Collins
JV
,
Barnes
PJ
.
Dose-dependent onset and cessation of action of inhaled budesonide on exhaled nitric oxide and symptoms in mild asthma.
Thorax
.
2002
;
57
(
10
):
889
896
[PubMed]
44
Jones
SL
,
Kittelson
J
,
Cowan
JO
, et al
.
The predictive value of exhaled nitric oxide measurements in assessing changes in asthma control.
Am J Respir Crit Care Med
.
2001
;
164
(
5
):
738
743
[PubMed]
45
Szefler
SJ
,
Mitchell
H
,
Sorkness
CA
, et al
.
Management of asthma based on exhaled nitric oxide in addition to guideline-based treatment for inner-city adolescents and young adults: a randomised controlled trial.
Lancet
.
2008
;
372
(
9643
):
1065
1072
[PubMed]
46
Petsky
HL
,
Cates
CJ
,
Li
A
,
Kynaston
JA
,
Turner
C
,
Chang
AB
.
Tailored interventions based on exhaled nitric oxide versus clinical symptoms for asthma in children and adults.
Cochrane Syst Database Rev
.
2009
(
4
):
CD006340
47
Petsky
HL
,
Cates
CJ
,
Lasserson
TJ
, et al
.
A systematic review and meta-analysis: tailoring asthma treatment on eosinophilic markers (exhaled nitric oxide or sputum eosinophils).
Thorax
.
2012
;
67
(
3
):
199
208
[PubMed]
48
Castro-Rodríguez
JA
,
Holberg
CJ
,
Wright
AL
,
Martinez
FD
.
A clinical index to define risk of asthma in young children with recurrent wheezing.
Am J Respir Crit Care Med
.
2000
;
162
(
4 pt 1
):
1403
1406
[PubMed]
49
Chang
TS
,
Lemanske
RF
 Jr
,
Guilbert
TW
, et al
.
Evaluation of the modified asthma predictive index in high-risk preschool children.
J Allergy Clin Immunol Pract
.
2013
;
1
(
2
):
152
156
[PubMed]
50
Matsui
E
,
Abramson
S
,
Sandel
M
;
American Academy of Pediatrics, Section on Allergy and Immunology
.
Clinical report: indoor environmental control practices and asthma management.
Pediatrics
. Available at http://pediatrics.aappublications.org/content/early/2016/10/27/peds.2016-2589. Accessed November 8, 2016

Chitra Dinakar, MD, FAAP

Bradley Chipps, MD, PhD, FAAP

Elizabeth C. Matsui, MD, MHS, FAAP, Chair

Stuart L. Abramson, MD, PhD, AE-C, FAAP

Chitra Dinakar, MD, FAAP

Anne-Marie Irani, MD, FAAP

Jennifer S. Kim, MD, FAAP

Todd A. Mahr, MD, FAAP, Immediate Past Chair

Michael Pistiner, MD, FAAP

Julie Wang, MD, FAAP

Thomas A. Fleisher, MD, FAAP

Scott H. Sicherer, MD, FAAP

Paul V. Williams, MD, FAAP

Debra L. Burrowes, MHA

Julie P. Katkin, MD, FAAP, Chair

Kristin N. Van Hook, MD, FAAP

Lee J. Brooks, MD, FAAP

Bonnie B. Hudak, MD, FAAP

Richard M. Kravitz, MD, FAAP

Shrutim Paranjape, MD, FAAP

Michael S. Schechter, MD, FAAP, Immediate Past Chair

Girish D. Sharma, MD, FAAP

Dennis C. Stokes, MD, FAAP

Laura Laskosz, MPH

Competing Interests

POTENTIAL CONFLICT OF INTEREST: The authors have indicated they have no potential conflicts of interest to disclose.

FINANCIAL DISCLOSURE: The authors have indicated they do not have a financial relationship relevant to this article to disclose.