Difficult-to-control asthma management through the use of a specific protocol

The present study is a critical review of difficult-to-control asthma, highlighting the characteristics and severity of the disease. It also presents a protocol for the management of patients with this asthma phenotype. The protocol, which was based on relevant studies in the literature, is described and analyzed.

INTRODUCTION

The worldwide prevalence of asthma is estimated at 10%, which makes it a public health problem which has generated considerable interest among researchers.1-4

In Brazil, the local arm of the International Study of Asthma and Allergies in Childhood (ISAAC), which concentrates on children and adolescents, revealed a high prevalence of asthma symptoms (20-25%) in most Brazilian cities.5,6 Among prepubescent children, asthma is more common among boys. However, among adolescents and adults, women are more often affected and experience greater asthma severity than those in other groups.7,8

Another major facet indicating the influence of asthma on morbidity and mortality in Brazil is revealed by data regarding hospitalizations for asthma via the Brazilian Public Unified Health Care System, which is responsible for the treatment of 70-75% of the population. The number of hospitalizations annually for asthma has been in decline since 2000, when it peaked at 397,000 (Figure 1).9 Factors that might have contributed to this decrease in morbidity include the development and implementation of programs for the treatment of asthma in Brazil through which asthma medication is made available to patients at no charge. However, it is necessary to improve upon the activities already initiated and make them more homogeneous throughout the country.

Figure 1.

Hospitalization due to asthma in Brazil as a whole and in São Paulo, Brazil in particular, according to data from the Information Technology Department of the Brazilian Unified Health Care System.- Hospitalization due to asthma in Brazil as a whole and in São Paulo, Brazil in particular, according to data from the Information Technology Department of the Brazilian Unified Health Care System.

IC: inhaled corticosteroid; LABA: long-acting β₂ agonist

The Hospital das Clínicas of the School of Medicine of São Paulo University (HC-FMUSP), located in the city of São Paulo, Brazil, is a tertiary care facility and, therefore, receives cases that are more complex and severe than those in other hospitals. It should be kept in mind that difficult-to-control asthma, although accounting for no more than 5% of all asthma cases, is responsible for approximately 50% of the overall costs related to asthma treatment in Brazil. It is also associated with greater morbidity and mortality, a higher risk of emergency room treatment being needed, and of hospitalization, respectively, being 15 and 20 times greater for such patients than for those with less severe forms of asthma.10-13

Challenged by the high prevalence of asthma and by high asthma-related morbidity, which has a strong socioeconomic impact, various health care facilities, medical societies, and organizations have developed protocols and consensuses for a more effective approach to asthma and difficult-to-control asthma.1,12,14-17

In this context, a difficult asthma management protocol (DAMP) was developed at the Asthma Outpatient Clinic of the HC-FMUSP Department of Clinical Immunology and Allergy. The protocol requires the analysis of various situations which have been grouped into three blocks (Figure 2). Simultaneously, a line of research dedicated to this clinical entity was developed, allowing the execution of various studies that have been published in indexed journals and presented at national and international conferences. In addition to the DAMP, the development and implementation of electronic medical records has promoted the treatment of, education regarding, and research into asthma.18

Figure 2.

Protocol for the treatment of patients with difficult-to-control asthma.- Protocol for the treatment of patients with difficult-to-control asthma.

VCD: vocal cord dysfunction; ABPA: allergic bronchopulmonary aspergillosis; NSAIDs: nonsteroidal anti-inflammatory drugs; CSS: Churg-Strauss syndrome

Besides the protocol discussion, the authors reviewed the literature, mainly the Global Initiative for Asthma (GINA) guidelines, to classify the recommendations presented here on the basis of level of evidence (Figure 3).

Figure 3.

Description of levels of evidence (Adapted from GINA).- Description of levels of evidence (Adapted from GINA).

DISCUSSION

Difficult-to-control Asthma

By consensus, the term “difficult-to-control asthma” is used in medical literature worldwide. However, various other terms, such as “difficult asthma,” “difficult-to-treat asthma,” “resistant asthma” and “refractory asthma,” are also used. Most patients with difficult-to-control asthma have severe corticosteroid-dependent asthma or severe corticosteroid-insensitive asthma.

The 2006 Latin American Consensus on Difficult-to-Control Asthma defined the disease as an asthma that is insufficiently controlled despite appropriate therapeutic strategies adjusted to the degree of clinical severity of the disease.19,20 Although this definition is subject to a certain degree of subjectivity, it represents a group of patients who have specific characteristics and, therefore, should be approached in a special manner. With the purpose of making the diagnosis of difficult-to-control asthma more objective, various consensuses have proposed primary and secondary criteria. The Latin American Consensus has defined difficult-to-control asthma as asthma that meets at least one of the primary criteria and one of the secondary criteria or both primary criteria (Figure 4).19 In practice, it can be said that patients have difficult-to-control asthma if they present asthma that has been treated with systemic corticosteroids for more than six months or that remains uncontrolled despite the administration of high doses of an inhaled corticosteroids (IC) in combination with a long-acting β₂ agonist (LABA).

Figure 4.

Criteria for the diagnosis of difficult-to-control asthma.- Criteria for the diagnosis of difficult-to-control asthma.

SC: systemic corticosteroid; IC: inhaled corticosteroid; LABA: long-acting β₂ agonist; FEV₁: forced expiratory volume in one second; PEF: peak expiratory flow; PFT: pulmonary function test

After the 2006 revision of the Global Initiative for Asthma (GINA) guidelines, the criteria used to classify asthma patients as having controlled asthma became stricter: presenting with nearly asymptomatic disease (no nighttime symptoms and a maximum of two episodes of daytime symptoms);presenting with no exacerbations;using rescue medication twice a week at most;presenting with no limitations in physical activity;presenting with no adverse reactions to the drugs used;and presenting with normal pulmonary function test results.

As of yet, there is no consensus regarding the best manner to measure asthma control (Figure 5). Some of these measurements are routinely used during outpatient treatment, whereas others are used specifically in clinical research. These measurements do not always correlate with each other, underscoring the need to analyze the results of various methods of assessment in conjunction with each other. For instance, forced expiratory volume in one second (FEV₁), one of the indices that is most widely used to monitor patients, might not correlate with levels of exhaled nitric oxide or with scores on questionnaires designed to measure asthma control.21-23 The latter were created for the purpose of structuring and standardizing the evaluation of patients, thereby including clinical data and pulmonary function data, as well as data regarding inflammation (Figure 6). Some questionnaires have been validated and are easy to administer, as well as capable of being graded by scores that allow patient monitoring over a period of time.

Figure 5.

Assessment of asthma control.- Assessment of asthma control.

FEV₁: forced expiratory volume in one second; PEF: peak expiratory flow; ACT: asthma control test; ACQ: asthma control questionnaire; ATAQ: asthma therapy assessment questionnaire; ACSS: asthma control scoring system; AQLQ: asthma quality of life questionnaire

Figure 6.

Questionnaires to measure asthma control.- Questionnaires to measure asthma control.

ACT: asthma control test; ACQ: asthma control questionnaire; ATAQ: asthma therapy assessment questionnaire; ACSS: asthma control scoring system; FEV₁: forced expiratory volume in one second; PEF: peak expiratory flow; and %ES: percentage of eosinophils in sputum; ND: not determined

Asthma is currently regarded as a syndrome, or at least as a disease that has various phenotypes.24-26 The two principal phenotypes, which have clear and distinct characteristics, are allergic and non-allergic asthma. In addition to the classification according to etiology, asthma can be classified according to severity and level of control.

In patients with allergic asthma, the onset of symptoms tends to be earlier, the disease progresses in a more benign manner, the rate of hypersensitivity to non-steroidal anti-inflammatory drugs (NSAIDs) is lower, and the clinical history (personal and family) usually includes other atopic diseases (Figure 7). Exacerbations in these patients are characteristically related to exposure to aeroallergens. Patients with allergic asthma present with increased serum levels of total and specific immunoglobulin E (IgE). Specific IgE can be detected by in vivo tests (immediate skin test: skin prick test and intradermal test) and by in vitro tests (enzyme immunoassays). In rare cases, specific IgE is detected only at the site of the allergic process (local allergy).27,28

Figure 7.

Differences between allergic asthma and non-allergic asthma.- Differences between allergic asthma and non-allergic asthma.

NSAID: nonsteroidal anti-inflammatory drug; IgE: immunoglobulin E

In both phenotypes, there is generally eosinophilic inflammation of the airways.29 However, neutrophilic infiltration is more common in non-allergic asthma. Studies have demonstrated that the number of neutrophils in induced sputum is significantly greater in patients with severe asthma than in those with mild asthma or in individuals without asthma.30 Neutrophilic inflammation has also been reported in acute exacerbations of the disease and in sudden-onset fatal asthma.31-33

Respiratory allergy is an example of a type I hypersensitivity reaction in which the allergen is presented to the T lymphocyte that will mediate a Th2 immune response, forming IgE antibodies.34-36 It is quite characteristic for a type I hypersensitivity reaction to occur in two phases: an immediate phase, occurring as a result of the degranulation of mast cells and basophils, and a late phase, occurring due to the recruitment (through chemotaxis) of other cells, such as eosinophils, which migrate to the site of inflammation. When the process becomes chronic, these phases overlap.37,38 In fact, the immune response is a network, within which various cells communicate through the secretion of cytokines and adhesion molecule expression. A recent study suggested that allergic asthma can be triggered by a Th2 response, even without the presence of IgE.39

In contrast to allergic asthma, the pathophysiology of which is well-characterized, the etiology of and mechanisms involved in non-allergic asthma remain unclear. Some of the possibilities include allergy triggered by unknown antigens (fungi), persistent infection (caused by Chlamydia trachomatis, Mycoplasma sp. or viruses), and autoimmunity.

A prospective study involving 300 consecutive patients referred to us with working diagnoses of asthma and rhinitis revealed that 68.4% of them presented sensitization to at least one aeroallergen, as demonstrated by skin prick tests. The allergens that presented the highest rates of sensitization were, in decreasing order, dust mite allergens, cockroach allergens, and cat allergens.40

Difficult-to-control asthma can also be considered a specific phenotype of asthma, and, as suggested by the 2006 Latin-American Consensus on Difficult-to-Control Asthma, difficult-to-control asthma can be subdivided into other phenotypes: labile asthma type I and II, corticosteroid-resistant asthma, corticosteroid-dependent asthma, and near-fatal asthma.19,41

Various studies, such as the one by the European Network For Understanding Mechanisms Of Severe Asthma (ENFUMOSA study), which was conducted in 2003, have characterized difficult-to-control asthma.8 According to the study, this phenotype was more prevalent in non-allergic asthma and among females. In adults, the female/male ratio was 1.6:1 for asthma in general, compared with 4.4:1 for difficult-to-control asthma. Inflammation with a predominance of neutrophils was also more common in this phenotype;a prevalence of 36% was observed, in comparison with a prevalence of 28% in all asthma cases.

Although there is a consensus that most types of severe asthma are non-allergic, the Epidemiology and Natural History of Asthma: Outcomes and Treatment Regimens study (TENOR study) showed that, in children, IgE levels are markers of severity.42

We investigated hospital morbidity due to asthma, analyzing the factors associated with the need for hospitalization due to asthma.43 Most of the patients in our study were female and presented with moderate or severe asthma. Rhinosinusitis predominated among the associated diseases and respiratory infections were the principal cause of hospitalization. Most patients presenting with a history of smoking had been able to quit the habit. The three principal factors associated with hospitalization were as follows: poor treatment adherence, underuse of corticosteroids, and prior hospitalization.

Various studies have evaluated the relationship between the severity of asthma and genetic polymorphism:44-51

• •

  IL-4 and its receptor.

• •

  Genes related to fibrosis (transforming growth factor-beta 1 and monocyte chemoattractant protein-1).

• •

  Genes related to pharmacogenetics (aspirin-intolerant asthma;responses to corticosteroids, β-2 adrenergic agonists and leukotriene antagonists).

Exposure to tobacco smoke and continuous exposure to aeroallergens, principally dust mite aeroallergens, fungi aeroallergens, cockroach aeroallergens, and rat aeroallergens, are also associated with severe asthma (Evidence B).52-55 The same occurs with infections caused by the respiratory syncytial virus, Chlamydia trachomatis or Mycoplasma sp.56

The Protocol

The DAMP, developed in the HC-FMUSP Department of Clinical Immunology and Allergy, is based on three blocks (sets) of measures (Figure 2).

Block I

In the first block, the measures focus on analyzing situations that are more commonly associated with asthma that remain uncontrolled despite the use of theoretically appropriate treatments. In this block, it is suggested that the diagnosis of the disease be confirmed and that environmental controls, treatment adherence, and medication use be evaluated (Evidence B) and that treatment be optimized (Evidence A).

Studies have reported that, in most cases, by improving the evaluation and treatment of these patients, asthma can be controlled without the continuous use of systemic corticosteroids or immunosuppressants (Evidence A).19,57 In a study of Leal OM, the potentially aggravating factors of asthma were, in decreasing order of frequency, as follows: unsatisfactory knowledge of the disease, incorrect techniques in terms of using medications, gastroesophageal reflux, inappropriate environmental controls, poor treatment adherence, rhinosinusitis and polyposis, emotional factors, allergic bronchopulmonary aspergillosis (ABPA), vocal cord dysfunction (VCD), failure to use the recommended IC, and intolerance to NSAIDs.58

The Spanish Consensus on Asthma Management has divided difficult-to-control asthma into two subgroups: true difficult-to-control asthma and false difficult-to-control asthma. False difficult-to-control asthma, perhaps the more common of the two, is that syndrome in which poor control is associated with factors that are not intrinsic to the disease itself, such as incorrect diagnoses of asthma and poor treatment adherence. This discussion is a more conceptual one since all patients with clinical profiles consistent with difficult-to-control asthma should initially be regarded as having the disease so that the factors that influence disease control can be properly identified, approached, and modified.15

According to the DAMP, the diagnosis of asthma should first be confirmed because asthma may be mistaken for or, more commonly, accompanied by chronic obstructive pulmonary disease or congestive heart failure. In some patients who smoke, it is extremely difficult to distinguish between pulmonary involvement due to asthma and that due to chronic obstructive pulmonary disease.

Whether environmental control is being properly performed and whether all allergens and irritants involved have been identified and avoided should also be investigated. The treatment of respiratory allergies has traditionally been divided into three parts: environmental control, pharmacological treatment, and immunotherapy. The division is purely instructive since these three treatment modalities complement one another and should be employed in conjunction with each other.

Although there is a rationale, as well as evidence for the need to adopt preventive measures to reduce the number of aeroallergens in the environment (Evidence B), some studies have been unable to confirm the impact of such measures on disease control.59,60 The difficulty in confirming the effectiveness of environmental control is due, at least in part, to poor treatment adherence and the complexity of asthma, a disease that results from the interaction between various environmental and genetic factors.61 Among the irritants that are associated with a less favorable evolution of asthma, smoking and pollution are noteworthy (Evidence B).62-64

In patients with difficult-to-control asthma, the possibility of occupational asthma should always be considered and the knowledge that avoidance of identified allergens improves disease control (Evidence A).65 Specific bronchial provocation using allergens to confirm the etiology of asthma is rarely performed in routine clinical practice. However, it is an important tool for the diagnosis of inconclusive clinical cases and for the conducting of research.66,67 Specific bronchial provocation is safe, provided that it is performed in a standardized manner which follows protocols.68-73

It is likely that the most common causes of uncontrolled asthma are poor treatment adherence and insufficient knowledge on the part of the patient, which results, for example, in the incorrect use of medication. It is estimated that asthma treatment adherence ranges from 30 to 50%.74 After a trusting relationship has been established between the health professional and the patient, the importance of treatment adherence should be discussed and measures to ensure that the patient remembers to take the medication should be proposed (Evidence B). Open dialogue, through clear and direct questions, is the most appropriate method for determining whether the proposed treatment regimen is being followed.75

A series of studies conducted on various continents revealed that most asthma patients have uncontrolled asthma, are not aware of that fact, have not been properly educated, and are not being correctly monitored (Figure 8). Underuse of ICs, which is observed even among patients with extremely severe asthma, is among the principal causes of uncontrolled asthma.76-79 One study demonstrated eosinophilic inflammatory infiltration throughout the airways of deceased individuals who had presented with fatal asthma. Many of these individuals were not treating their asthma regularly and were not using ICs. 80

Figure 8.

Rate of severe exacerbations of asthma in the last year.- Rate of severe exacerbations of asthma in the last year.

Although physicians should develop strategies of education and guidance (which include giving patients written treatment plans - Evidence A), some studies have demonstrated that health professionals are not always trained in how to do that.81,82 Patients should know that the respiratory symptoms of asthma result from an inflammatory process in the airways, that there are drugs to treat exacerbations and others used as maintenance drugs and that, although asthma is chronic, the disease can be controlled through treatment, improving quality of life and reducing morbidity.83 There are various devices for administering the drugs through inhalation, and the techniques for using such devices should be taught and checked at every medical visit as part of the examination. The use of a peak expiratory flow meter should also be demonstrated because this will allow home monitoring of pulmonary function (Evidence B).

Regarding treatment optimization, it is assumed that the amount of medication prescribed should be the lowest possible to maintain and control the asthma.

The 2006 update of the GINA guidelines proposed a new asthma classification based on disease control evaluation: controlled asthma, partially controlled asthma, and uncontrolled asthma. As previously described, the criteria for this new classification are also rigorous.

The Gaining Optimal Asthma controL (GOAL) study, conducted in 2004, had a great influence on the changes in the GINA guidelines.84 It showed that most patients with asthma do not fully respond to the treatments they were given. However, treatment response can be achieved through more rigorous approaches. The GOAL study also suggested that asthma control can be achieved more rapidly and in a greater percentage of patients through the use of ICs in combination with LABAs.

The Salmeterol Multicenter Asthma Research Trial (SMART) study, conducted in 2006, put in check the indiscriminate use of LABAs in patients with asthma.85 The SMART was a multicenter, randomized, double-blind, placebo-controlled study that evaluated 26,355 patients. There was a small increase in mortality related to the use of LABAs, principally in African-American patients.

The GINA currently recommends a combination therapy (ICs and LABAs) for patients with moderate or severe asthma that has not been controlled by IC use alone. It is known that, when used continuously, LABAs should always be prescribed in combination with ICs.86 However, the question regarding the dose of IC with which LABAs should first be combined remains unanswered. Is it better for patients to receive high doses of an IC or moderate doses of an IC in combination with a LABA?

In recent decades, the use of ICs has become the standard treatment for patients with persistent asthma. The administration through inhalation has improved disease control, reducing mortality and, simultaneously, the side effects triggered by the use of systemic steroids (Evidence A).87

However, certain local effects, such as oropharyngeal candidiasis and dysphonia, can occur and can lead patients to discontinue treatment.88 With the increase in the use and doses of ICs, studies have also reported esophageal candidiasis as being a complication of asthma treatment.89-91 Esophageal candidiasis is underdiagnosed and often oligosymptomatic. The diagnosis is made only when there is a high degree of suspicion, principally in patients using high doses of ICs.

It has been demonstrated that only by changing ICs and inhalers can this complication be avoided and treated.92 Another interesting observation is that, just as oral asepsis after IC use prevents oral moniliasis, the ingestion of fluids and solids may prevent and treat esophageal infection.93 This effectively constitutes esophageal lavage and removes the medication deposited in the mucosa.

The treatment of asthma should always be adjusted so that the morbidity and mortality from the disease are as low as possible, providing patients with a better quality of life. Complete control should always be the goal. However, when this goal cannot be achieved, the objective of the treatment should be to attain the best response and the fewest adverse reactions. Once asthma is properly controlled by a treatment regimen, the medication dose should be progressively reduced to the minimum required to maintain disease control.

Block II

In the second block of the DAMP, co-morbidities and associated diseases should be investigated and identified because the treatment of these diseases aids in controlling asthma.

We have recently analyzed the data obtained from the electronic medical records of 245 patients treated for severe asthma.94 Rhinitis, gastroesophageal reflux disease (GERD), and bronchiectasis were the most common co-morbidities observed, showing a high prevalence. Therefore, in patients with severe asthma, associated diseases should be investigated as the cause of respiratory symptoms and uncontrolled asthma. Some of the principal entities that aggravate the progression of asthma are described and discussed below.

Rhinosinusitis

Rhinitis is an inflammatory disease of the nasal mucosa that is clinically characterized by four principal symptoms: rhinorrhea, sequential sneezing, pruritus, and nasal congestion.95,96 In the case of allergic rhinitis, the inflammatory process is induced by an IgE-mediated immune response.

Rhinitis-related morbidity is high and represents a heavy socioeconomic burden due to direct and indirect costs.95-101 The estimated prevalence of allergic rhinitis in the general population is 30%, and allergic rhinitis is the most common chronic disease in children, which makes it a serious public health problem.95,96,102,103

The ARIA consensus was published in 2001.96 In addition to some new conceptual modifications regarding rhinitis, such as a change in the classification of the disease, the ARIA highlighted the importance of being aware of the influence that the upper airways exert on the lower airways and vice-versa (Figure 9).96,104

Figure 9.

Objectives of the Allergic Rhinitis and its Impact on Asthma initiative.- Objectives of the Allergic Rhinitis and its Impact on Asthma initiative.

Allergic rhinitis and allergic asthma are currently recognized as manifestations of a single entity, “chronic allergic respiratory disease,” also known as “united airway disease.” There is epidemiological, pathophysiological, and clinical evidence to support an integrated view of these diseases, allowing a better understanding of their interactions (Figure 10).96,97,105-108 The great majority of patients with asthma have rhinitis, the latter being a risk factor for the development of the former.

Figure 10.

Pathophysiological evidence for the interaction between allergic rhinitis and allergic asthma.- Pathophysiological evidence for the interaction between allergic rhinitis and allergic asthma.

Some studies have demonstrated that the presence of severe rhinitis in patients with asthma is associated with less favorable evolution. It has also been shown that the treatment of nasal symptoms can be beneficial to the lower airways (Evidence A), reducing the number of emergency room visits and hospitalizations, as well as the severity of bronchial hyperreactivity.106,109-112

These studies and others with similar results do not suggest that patients with rhinitis and asthma should be treated with nasal medications alone;what they do recommend is that the teachings of the ARIA initiative should not be forgotten.

Gastroesophageal Reflux Disease (GERD)

Patients with GERD can present with respiratory manifestations. The prevalence of GERD is higher in patients with asthma than in the general population, and GERD is associated with difficult-to-control asthma. However, there is no definitive scientific evidence that the treatment of one of the two diseases translates to a more favorable progression of the other (Evidence C).

Asthma and GERD frequently coexist.113 Concomitance between symptoms of dyspnea and reflux is quite common, and large-scale studies have shown that the degree of reflux can be as much as 60% greater in individuals with asthma than in those without.114 In a study conducted in the United Kingdom, the prevalence of GERD symptoms among patients with difficult-to-control asthma was found to be 75%.115

It has been shown that GERD exacerbates asthma through mechanisms involving vagus nerve stimulation (esophagobronchial reflex) or microaspiration of gastric contents into the airways.

Adverse Drug Reactions

Aspirin-induced asthma is a clinical entity characterized by asthma and intolerance to aspirin or NSAIDs.116 Aspirin-induced asthma and nasal polyposis (Samter triad) are associated with an increase in asthma severity.117,118

Although hypersensitivity to NSAIDs and aspirin affects only 0.6-2.5% of the general population of adults, it occurs in 5-20% of adults with asthma.119 It has previously been demonstrated that many patients are not able to perceive this exacerbation. In a study conducted in Europe and involving 500 patients diagnosed with aspirin-intolerant asthma, 90 (18%) were unable to perceive any worsening of the symptoms prior to the provocation test.120

Vocal Cord Dysfunction (VCD)

The features of VCD include episodes of involuntary paradoxical movements caused by vocal cord adduction during respiration and resulting in airway obstruction. The clinical profile is characterized by stridor, dyspnea, and wheezing, principally in the cervical region. Although VCD generally is seen in patients with asthma, it can also occur in an isolated form in individuals without respiratory disease.

The prevalence of VCD, which is higher in patients with difficult-to-control asthma, has yet to be well established.121 In Brazil, the prevalence of VCD in patients with severe asthma and difficult-to-control asthma were found to be 17.5% and 19.5%, respectively.122 However, VCD is commonly underdiagnosed, which is responsible for the low reported prevalence of this disease at various health care facilities.

The pathophysiology of VCD is unknown, and no organic cause has yet been found. The most accepted hypothesis is that its etiology is psychogenetic and that attacks of VCD are commonly triggered by psychological factors.123-126

Two factors make VCD more intriguing and more difficult to diagnose than other similar diseases. First, there is a confounding overlap between asthma and VCD attacks when they coexist.121,124 Second, VCD appears as attacks, and certain patients, especially those with VCD in isolation, can be asymptomatic between attacks. Since there are no diagnostic criteria for VCD, clinical suspicion is based on discrepancies between the clinical profile, the complementary test results, and the therapeutic response.

A definitive diagnosis of VCD can be obtained by means of laryngoscopy. When performed during an attack, it shows a typical pattern, which consists of the adduction of the anterior two thirds of the vocal cords during inspiration, forming a posterior cleft with a “diamond shape.”121,124

Many patients with VCD are misdiagnosed as having severe asthma or difficult-to-control asthma and, therefore, receive inadequate or inappropriate treatment since VCD treatment is based on psychotherapy and speech therapy (Evidence C). It should be noted that these patients receive the same treatment as do those with difficult-to-control asthma, including the continuous use of systemic corticosteroids. In addition to producing a limited clinical response, this treatment regimen has undesirable side effects (Evidence B). However, since most patients with VCD also suffer from asthma, the latter should not be ignored.

Recently, a specific questionnaire designed to raise awareness of the possibility of VCD was developed in order to identify patients who are more likely to be diagnosed with the disease (Figure 11).122 In essence, the questionnaire attempts to identify whether there are discrepancies or inconsistencies between the clinical profile, the complementary tests, and the treatment of the patient.

Figure 11.

Specific questionnaire for the clinical suspicion of vocal cord dysfunction.- Specific questionnaire for the clinical suspicion of vocal cord dysfunction.

Q: question;FEV₁: forced expiratory volume in one second; and PEF: peak expiratory flow

Allergic Bronchopulmonary Aspergillosis (ABPA)

The complex disease ABPA is triggered by a hypersensitivity reaction to allergens of the fungus Aspergillus fumigatus. The prevalence of ABPA among asthma patients sensitized to A. fumigatus in Brazil has been reported to be 20%.127

The course of ABPA includes periods of exacerbation and remission. The disease can progress to a phase in which the patient presents with central bronchiectasis and pulmonary fibrosis, resulting in chronic respiratory failure.128

Since ABPA is accompanied by cystic fibrosis or asthma (especially difficult-to-control asthma), it is another disease in which the diagnosis is complicated. The challenge is to diagnose ABPA in its initial stages, when only the serological markers are present and the processes of cicatrization/fibrosis are not yet evident (ABPA with central bronchiectasis). Unfortunately, ABPA is often diagnosed only after years of monitoring, making it difficult to prevent irreversible lung damage.128-131

Some ABPA markers are difficult to detect (especially at the early stages of the disease) and, in general, the markers do not present simultaneously during a single evaluation. At least three factors make it difficult to diagnose the disease:

• 1)

  ABPA manifests as attacks.

• 2)

  The treatment of ABPA, which consists principally of using systemic corticosteroids, hinders with the diagnostic investigation.

• 3)

  The current methods for detecting specific antibodies (IgE and IgG) are not accurate or easily reproduced.

Some studies, especially those involving patients with cystic fibrosis, have reported that, based on the humoral response to recombinant allergens, it is possible to distinguish between ABPA patients and asthma patients sensitized to A. fumigatus, but without ABPA.132,133 Other studies, however, have reported that determination of the serum levels of IgE against recombinant allergens of A. fumigatus does not aid in diagnosing ABPA or in confirming sensitization to the fungus.134,135

It has been reported that there is a discrepancy between the intradermal test results and the serology results in patients suspected of having ABPA. Intradermal tests seem to be more sensitive, with late reactions having been reported.136

In this context, the diagnosis of ABPA remains complex and challenging.

Immunodeficiencies

Immunodeficiencies with recurrent respiratory infections are included in the differential diagnosis of asthma. However, when the two diseases are present in the same patient, the infections make asthma control difficult and they may trigger asthma exacerbations.

Secondary immunodeficiencies are more common than are primary immunodeficiencies and, in patients with asthma, the most prevalent type of immunodeficiency is that which results from corticosteroid therapy.137

Among the primary immunodeficiencies, the most prevalent are selective IgA immunodeficiency and common variable immunodeficiency (CVID), both of which are responsible for pulmonary infections and respiratory manifestations.138,139 The prevalence of respiratory impairment is high, and 25% to 50% of the patients present with bronchiectasis, obstructive pulmonary diseases, or restrictive pulmonary diseases.140,141 Recurrent infections are the principal cause of pulmonary involvement. However, a chronic inflammatory process, the etiopathogenesis of which remains unclear, is also observed in the lungs of these individuals.142,143 These data warrant intensive monitoring of the respiratory system of CVID patients and justify their treatment with gamma-globulin therapy, which has changed the prognosis of the disease (Evidence A).142,143

Many patients with CVID remain symptomatic, with respiratory complaints. These symptoms can mimic and be mistaken for those of asthma, and it is extremely difficult to confirm the diagnosis of asthma, as well as to determine the allergic etiology of asthma in patients with CVID.

We showed that in CVID patients, in addition to pulmonary function testing, bronchial provocations can aid in the diagnosis of asthma and can help to confirm the allergic etiology of the disease since the vast majority of patients present specific serum IgE that cannot be detected by skin tests or by in vitro tests.39

Although patients with CVID synthesize low quantities of antibodies, perhaps the production of IgE in the airways can be enough to trigger allergic asthma. Another hypothesis has to be considered: the existence of a Th2 immune response with participation and activation of T lymphocytes, mast cells and eosinophils, without the presence of the IgE antibody.

Churg-Strauss Syndrome

Churg-Strauss syndrome (CSS) is a necrotizing systemic vasculitis of medium and small blood vessels characterized by asthma, eosinophilia, and eosinophilic or granulomatous tissue inflammation. It is currently recognized as one of the antineutrophil cytoplasmic antibody (ANCA)-associated vasculitides which is present in half of all CSS patients.144-146

Asthma and upper respiratory symptoms are present in nearly all CSS patients, besides the presence of other manifestations of systemic vasculitis. The syndrome manifests in three consecutive phases: a prodromal phase consisting of respiratory manifestations (rhinosinusitis and asthma), a second phase consisting of peripheral blood eosinophilia and eosinophilic tissue infiltrates, and a third phase consisting of systemic vasculitic manifestations.147-150

Corticosteroids are the cornerstone of CSS therapy and provide control of disease activity in the great majority of cases (Evidence A). However, 25-50% of CSS patients relapse within two years of achieving remission and a substantial proportion of patients present adverse drug reactions with significant morbidity.147-149,152 Asthma is not considered in the definition of CSS remission, and most patients continue to present with asthma and upper respiratory symptoms, requiring ongoing treatment.

We reported the first case of a patient with CSS who received anti-IgE antibodies for the treatment of difficult-to-control asthma.153,154 In parallel with the description of our clinical case, there were case reports of patients who developed CSS during anti-IgE antibody use.155-157 These studies have sparked a discussion as to whether omalizumab can trigger CSS, a discussion that is similar to that regarding anti-leukotrienes. After the analysis of the cases, it is argued that the patients probably had CSS before the use of the anti-IgE antibody and that the disease was masked by the use of systemic corticosteroids. The use of the anti-IgE antibody allowed the discontinuation of the systemic corticosteroids, increasing the activity of CSS and allowing the diagnosis to be made.158-162

Discontinuation of the use of systemic corticosteroids in patients with asthma, especially in those with severe asthma who are suspected of having CSS, should be undertaken with care.

Block III

After the situations and co-morbidities described in Blocks I and II have been identified and controlled, additional measures might be necessary.

Due to the specialization and deepening of knowledge in the health area, diseases that are more severe and complex might be approached more effectively if multiprofessional and multidisciplinary teams were to be involved. Some studies have demonstrated the benefits of physical therapy and physical exercise to treat asthma (Evidence C).163-165 Psychological evaluation can also be beneficial, principally in prolonged and severe cases (Evidence C). It has been shown that the prevalence of symptoms of anxiety and depression is higher in patients with asthma than in patients with chronic obstructive pulmonary disease.166

In a minority of patients, prolonged, continuous use of systemic corticosteroids, often at high doses, is required. When the use of systemic corticosteroids is discontinued, asthma control worsens. In patients with this type of asthma, which is designated corticosteroid-dependent asthma, the adverse effects of the treatment become a serious problem (Evidence A).

A small portion of patients do not respond adequately to glucocorticoids, regardless of the dosage. These patients are designated corticosteroid-insensitive or corticosteroid-resistant, and they also present with severe side effects.167 The lack of response to the medication might be only partial and might occasionally be reversed by treating the inflammatory process. Clinically, patients with corticosteroid-insensitive asthma are those who present with an FEV₁ < 70% of the predicted value and who do not show a 15% and a 200 ml improvement in FEV₁ after treatment with prednisolone 40 mg (or equivalent), for 14 days. If there is no treatment response, the dose can be doubled for an additional 14 days.168

In cases in which insensitivity to corticosteroids is due to a reduction in the affinity between the drug and its receptor at least two mechanisms have been described.169,170 There can be genetic (inherited) modifications in the receptors or, more commonly, the inflammatory process induces a reduction in affinity.

Neutrophilic asthma is another phenotype of the disease that might not respond adequately to glucocorticoids.171-173 These drugs antagonistically induce and inhibit the apoptosis of eosinophils and neutrophils, respectively. There is controversy in the literature as to whether the neutrophilic infiltrate is the cause of airway inflammation or a consequence of the chronic use of corticosteroids. There is evidence that, in the bronchial mucosa of patients with difficult-to-control asthma, eosinophils predominate in some cases and neutrophils predominate in others (Evidence B). There are also two subgroups of fatal asthma: sudden-onset fatal asthma, which is accompanied by neutrophilic inflammation, and slow-onset fatal asthma, which is accompanied by eosinophilic infiltrate.32

Various drugs that somehow modulate inflammation have been used as alternative treatments in corticosteroid-insensitive and corticosteroid-dependent patients (Evidence C). Such drugs include colchicines, chloroquine, dapsone, macrolides, immunoglobulins, gold salts, azathioprine, cyclosporine, and methotrexate.19 Although some of these agents might be useful in treating certain patients, they do not have consistent effects and some of them have been associated with severe adverse reactions. In the absence of studies determining the subgroups of patients that would benefit the most from using these drugs, they should be prescribed on a case-by-case basis.

Omalizumab is a humanized anti-IgE monoclonal antibody that has recently been made available in Brazil for the treatment of difficult-to-control allergic asthma. The clinical effectiveness of omalizumab has been proven in various studies, principally with regard to the following parameters: exacerbations, quality of life, use of rescue medication, and reduction in the use of ICs (Evidence B).[174-176] The principal challenges facing the use of omalizumab are the correct characterization of the profile of patients who would benefit the most from anti-IgE antibody use and the limited access to the medication, which is principally due to its high cost.

CONCLUSIONS

Asthma is a chronic disease of high prevalence and a public health problem. It affects individuals of all ages and, if left uncontrolled, it causes limitations of activities of daily living and can lead to death.

The treatment of asthma, principally that of the allergic phenotype, has greatly evolved, and the vast majority of patients can present with controlled asthma, no symptoms, and normal pulmonary function. However, a small but significant portion of individuals with asthma present with difficult-to-control asthma, which is associated with high morbidity and cost.

The development of protocols for the treatment of difficult-to-control asthma, such as that which is presented in the present study, have allowed patients with this disease to be managed more effectively, possibly reducing morbidity and mortality and improving their quality of life. The objective of the protocols is to guide physicians; they do not exclude the idea of personalized medicine.