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5 курс / Пульмонология и фтизиатрия / Clinical_Manifestations_and_Assessment_of_Respiratory

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VT

IRV

ERV

RV

 

 

 

N or ↑

N or ↓

N or ↓

 

 

 

VC

IC

FRC

TLC

RV/TLC ratio

 

 

N or ↓

N or ↑

N or ↑

 

 

 

 

 

 

 

 

Arterial Blood Gases

Mild to Moderate Asthma Episode

Acute Alveolar Hyperventilation With Hypoxemia2 (Acute Respiratory Alkalosis)

pH

PaCO2

 

PaO2

SaO2 or SpO2

 

 

 

 

 

 

 

(but normal)

 

 

2See Fig. 5.2 and Table 5.4 and related discussion for the acute pH, PaCO2, and changes associated with acute alveolar hyperventilation.

Severe Asthma Episode (Status Asthmaticus)

Acute Ventilatory Failure With Hypoxemia3 (Acute Respiratory Acidosis)

pH4

PaCO2

4

PaO2

SaO2 or SpO2

 

 

 

 

 

 

 

(but normal)

 

 

3See Fig. 5.2 and Table 5.5 and related discussion for the acute pH, PaCO2, and changes associated with acute ventilatory failure.

4When tissue hypoxia is severe enough to produce lactic acid, the pH and values will be lower than expected for a particular PaCO2 level.

Oxygenation Indices5

Moderate to Severe Stages

QS/QT

DO26

VO2

 

O2ER

 

 

 

 

 

 

 

N

N

6The DO2 may be normal in patients who have compensated to the decreased oxygenation status with (1) an increased cardiac output, (2) an increased hemoglobin level, or (3) a combination of both. When the DO2 is normal, the O2ER is usually normal.

5, Arterial-venous oxygen difference; DO2, total oxygen delivery; O2ER, oxygen extraction ratio; QS/QT, pulmonary shunt fraction; , mixed venous oxygen saturation; VO2, oxygen consumption.

Abnormal Laboratory Tests and Procedures

Sputum Examination

Eosinophils

Charcot-Leyden crystals

Casts of mucus from small airways (Curschmann spirals)

IgE level (elevated in extrinsic asthma)

Asthma-COPD Overlap (ACO)

GINA provides an approach to distinguishing among asthma, COPD, and the overlap of asthma and COPD (termed asthma and COPD overlap [ACO]). Rather than attempting to provide a formal definition of ACO, GINA presents the clinical manifestations that identify and characterize ACO, assigning equal weight to features of asthma and COPD. Table 14.1 provides the highlights provided by GINA that distinguish the features of asthma, COPD, and ACO.

Radiologic Findings

Chest Radiograph (During an Asthma Episode)

Increased anteroposterior diameter (“barrel chest”)

Translucent (dark) lung fields

Depressed or flattened diaphragm

As the alveoli become enlarged during an asthma attack, the residual volume and functional residual capacity increase. This condition decreases the radiographic density of the lungs.

Consequently, the chest radiograph shows lung shadows that are translucent or darker than normal in appearance. Because of the increased residual volume, functional residual capacity, and total lung capacity, the diaphragms are depressed and flattened (Fig. 14.5).

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FIGURE 14.5 Chest x-ray film of a 2-year-old patient during an acute asthma attack.

General Management of Asthma

GINA provides an excellent clinical guideline program for the management and prevention of asthma. The complete GINA guidelines are readily available at http://www.ginasthma.org. An overview of GINA's global strategy for asthma management and prevention are discussed in the following text.

GINA's long-term goals for asthma management are symptom control (i.e., obtain control of the respiratory symptoms and maintain normal daily activities) and risk reduction of future exacerbations (e.g., removal of potential risk factors, such as smoking, beta-blockers, or allergen exposure, and checking for correct inhaler technique, adherence, and comorbidities, such as rhinitis, rhinosinusitis, obesity, obstructive sleep apnea, or depression or anxiety). The basic foundation to achieve these two goals is securing a strong partnership between the patient and the health care providers (e.g., good verbal and written communications and, importantly, presented at the patient's basic health literacy level). A good partnership enhances the asthma patient's ability to gain the knowledge, confidence, and skills necessary to self-manage his or her asthma. Along with a strong patient and health care provider partnership, GINA recommends a control-based asthma management program.

Control-Based Asthma Management Program

In a control-based asthma management program, the pharmacologic and nonpharmacologic treatment is a continuous cycle that entails the assessment of the patient's condition, treatment selection and/or adjustment (i.e., up-regulate or down-regulate the therapy), and the review of the patient's response (Fig. 14.6). In a control-based management program, both the symptom control and future risk for exacerbations need to be considered when selecting asthma treatment and assessing the patient's response to the therapy. The pharmacologic options for long-term treatment of asthma fall into the following three categories:

FIGURE 14.6 The control-based asthma management cycle. (Modified from Global Strategy for Asthma Management and Prevention, 2017, GINA. http://www.ginasthma.org.)

Controller medications: These agents are used for regular maintenance treatment. They decrease airway inflammation, control symptoms, and reduce the future risks for exacerbations and decreased lung function. Table 14.2 shows medications commonly used to control the symptoms of asthma.

TABLE 14.2

Controller Medications Used to Treat Asthma*

Generic Name

Brand Name

Inhaled Corticosteroids (ICSs)

 

Beclomethasone

QVAR

Flunisolide

Aerospan HFA

Fluticasone

Flovent HFA, Flovent Diskus, Arnuity Ellipta

Budesonide

Pulmicort Flexhaler

Mometasone

Asmanex Twisthaler, Asmanex HFA

Ciclesonide

Alvesco

Inhaled Corticosteroids and Long-Acting Beta2 Agents (Combined)

Fluticasone and salmeterol

Advair Diskus, Advair HFA

Budesonide and formoterol

Symbicort

Mometasone and formoterol

Dulera

Oral Corticosteroids

 

Methylprednisolone

Medrol, Solu-Medrol

Hydrocortisone

Solu-Cortef

Long-Acting Beta2 Agents (LABAs)

 

Salmeterol

Serevent Diskus

Leukotriene Inhibitors (Antileukotrienes)

Zafirlukast

Accolate

Montelukast

Singulair

Zileuton

Zyflo, Zyflo CR

Long-Acting Antimuscarinic Antagonists (LAMAs)

Tiotropium

Spiriva HandiHaler, Spiriva Respimat

Aclidinium

Tudorza Pressair

Umeclidinium

Incruse Ellipta

Xanthine Derivatives

 

Theophylline

Theochron, Elixophyllin, Theo-24

Oxtriphylline

Choledyl SA

Aminophylline

Generic

Dyphylline

Lufyllin

Agent to Reduce Eosinophilic Inflammation in Allergic Disease

Anti-interleukin-5

Mepolizumab (subcutaneous), reslizumab (intravenous)

Antiimmunoglobulin E (Anti-IgE)

 

Omalizumab

Xolair

*For the complete listing, doses, and administration of agents approved by the US Food and Drug Administration, visit the Drugs@FDA website (http://www.accessdata.fda.gov/scripts/cder/drugsatfda/).

Reliever (rescue) medications: These agents provide as-needed relief of asthma symptoms, including during worsening asthma or exacerbations. They are also helpful for short-term prevention of exercise-induced bronchoconstriction. Table 14.3 provides common reliever (rescue) medications used to treat the symptoms of asthma.

TABLE 14.3

Reliever Medications (Rescue Medications) Used to Treat Asthma*

Generic Name

Brand Name

Ultra-Short-Acting Bronchodilator Agents

Epinephrine

Adrenalin

Racemic epinephrine

Generic

Short-Acting Beta2 Agents (SABAs)

Albuterol

Proventil HFA, Ventolin HFA, ProAir HFA, AccuNeb HFA, Generic

Metaproterenol

Generic

Levalbuterol

Xopenex, Xopenex HFA, Generic

*For the complete listing, doses, and administration of agents approved by the US Food and Drug Administration, visit the Drugs@FDA website (http://www.accessdata.fda.gov/scripts/cder/drugsatfda/).

Add-on therapies for patients with severe asthma: These therapies may be considered when the patient continues to have symptoms and/or exacerbations despite optimized treatment with a high dose of controller medication and the treatment of modifiable risk factors.

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(Modified from
FIGURE 14.7

The Stepwise Management Approach to Control Asthma Symptoms and Reduce Future Risk

Based on the patient's current level of asthma control and current treatment regimen, GINA recommends one of five possible treatment steps that can be assigned to the patient. The preferred treatment at each step is based on (1) efficacy,

(2) effectiveness, (3) safety, and (4) the availability and cost of the treatment. In addition, the patient's asthma characteristics (phenotype), patient preference (i.e., goals and concerns), and practical issues (e.g., inhaler technique, adherence, and costs) need to be considered at each step.

Fig. 14.7 summarizes GINA's stepwise asthma management approach for adults, adolescents, and children 6 to 11 years.8 As can be seen, Step 1 through Step 5 progressively increase treatment medication options and intensity. In short, if the patient's asthma symptoms are not controlled on the current treatment program (e.g., Step 2), the treatment should be up-regulated to Step 3, Step 4, or Step 5 until control is achieved. Before considering a step-up, check for common problems such as poor inhaler technique, poor adherence, and environmental exposure to allergic allergens. When the control of the asthma symptoms has been maintained for at least 3 months, the ICS dose should be slowly titrated to the minimum dose that will maintain good symptom control and minimize exacerbation risk and potential side effects.

Stepwise asthma management for adults, adolescents, and children 6 to 11 years. ICS: inhaled corticosteroids; LABA: long-acting beta2-agonists; med: medium dose; OCS: oral cortisosteroids; SLIT: sublingual immunotherapy.

Global Strategy for Asthma Management and Prevention, 2017, GINA. http://www.ginasthma.org.)

STEP 1: As-Needed Reliever Inhaler

The preferred option is to start the patient on an as-needed short-acting beta2-agonist (SABA). SABAs are highly

effective in controlling asthma symptoms quickly (see Fig. 14.7). A second controller option is a regular low-dose ICS, in addition to as-needed SABA, in patients at risk for exacerbation. Table 14.2 provides common ICS agents used to control asthma symptoms.

STEP 2: Low-Dose Controller Medication Plus Needed Reliever Medication

The preferred option is to place the patient on a regular low-dose ICS, plus an as-needed SABA. ICSs at low doses have been shown to decrease asthma symptoms, improve lung function and quality of life, and reduce the risk for exacerbations and asthma-related hospitalizations and death. A second controller option is leukotriene receptor antagonists (LTRA), although they are considered less effective than ICSs. However, they may be appropriate for some patients who are unable or unwilling to use an ICS, the patient who experiences uncomfortable side effects from ICS, or the patient with concurrent allergic rhinitis. For the adult or adolescent patients, not previously on any controller treatment, a low-dose combination of ICS and long-acting beta2-agonists (LABAs) as the initial treatment has shown to reduce symptoms and improve lung

function when compared with a low-dose ICS alone. A low-dose sustained-released theophylline may be considered, although it has only a weak efficacy in asthma (see Fig. 14.7).

STEP 3: One or Two Controllers, Plus As-Needed Reliever Medication

The two preferred options for adults and adolescents are a combination of low-dose ICS/LABA as maintenance treatment, plus an as-needed SABA, or a combination low-dose ICS/formoterol (budesonide or beclomethasone) as both maintenance and reliever treatment. For adult patients with allergic rhinitis and sensitized to house dust mites, with exacerbations despite lowto high-dose ICS, consider adding sublingual allergen immunotherapy (SLIT) when the FEV1 is greater than 70% predicted. A second option for adults and adolescents is to increase the ICS to a medium dose or administer a

low-dose ICS, along with either an LTRA or a low-dose sustained-release theophylline. The preferred option for children 6 to 11 years is a moderate-dose ICS, plus an as-needed SABA (see Fig. 14.7).

STEP 4: One or Two Controllers Plus As-Needed Reliever Medication

The preferred option for adults and adolescents is a medium/high dose of ICS/LABA, plus an as-needed SABA or low-dose ICS/formoterol. For the adult patients with allergic rhinitis and sensitized to house dust mite, with exacerbations despite low-high dose ICS, consider adding SLIT when the FEV1 is greater than 70% predicted. A second option for adults and

adolescents with a history of exacerbations is tiotropium (long-acting muscarinic antagonist) by mist inhaler, a combination high-dose ICS/LABA, or a sustained-released theophylline. The preferred option for children 6 to 11 years is a referral for expert assessment and advice (see Fig. 14.7).

STEP 5: Higher Level Care and/or Add-On Treatment

The preferred option of Step 5 is referral for specialist investigation and consideration of add-on therapy. Treatment add-on options—if not already tried—include:

Add-on tiotropium (long-acting muscarinic antagonist) in patients 2 years or older with a history of exacerbation despite Step 4 treatment.

Add-on anti–immunoglobulin E (anti-IgE) (omalizumab) treatment for patients 6 years or older with a history of exacerbation despite Step 4 treatment.

Add-on anti–interleukin-5 treatment (subcutaneous mepolizumzab, intravenous reslizumab) for patients 12 years or older with severe eosinophilic asthma that cannot be controlled by Step 4.

Sputum-guided treatment for patients with persisting symptoms and/or exacerbations despite high-dose ICS or ICS/LABA. Treatment may be based on eosinophilia (>3%) in induced sputum.

Add-on low-dose oral corticosteroids (<7.5 mg/day prednisone equivalent) may be helpful for some adults with eosinophilia and/or severe asthma (see Fig. 14.7).

Add-on treatment with bronchial thermoplasty in adults with severe asthma.

Bronchial thermoplasty involves the use of therapeutic radiofrequency energy applied to the airway walls in patients with severe asthma. The procedure entails the insertion of a standard flexible bronchoscope through the patient's nose or mouth and into the lungs. The tip of the small-diameter catheter, which is threaded through the bronchoscope, is then introduced out into the bronchus and expanded to contact the walls of the targeted airway. As shown in Fig. 14.8 (see arrow), a controlled thermal energy is then applied to the bronchial airways, which in turn heats the airway tissues and shrinks the bronchial smooth muscles that cause the airways to constrict during an asthma episode. This treatment has been shown to cause acute epithelial destruction followed by regeneration in the epithelium, blood vessels, mucosa, and nerves. The bronchial smooth muscles, however, demonstrate no remarkable regeneration and, instead, are replaced by connective tissue.

The full treatment course includes three different bronchial thermoplasty procedures: One treatment for the left lower lung lobe, one treatment for the right lower lung lobe, and one treatment for both the right and left upper lobes. Each procedure is performed at least 3 weeks apart. Side effects include coughing, wheezing, and shortness of breath. Bronchial thermoplasty is indicated for patients with severe persistent asthma who are 18 years and older and whose asthma is not well controlled with longacting beta-agonists and ICSs. Patients who have been treated with bronchial thermoplasty have shown a reduction in severe asthma attacks, fewer visits to the emergency department, a drop in hospitalization for respiratory symptoms, and a decrease in days lost from work or school. Although this treatment has been shown to be safe and effective since it was first approved by the US Food and Drug Administration (FDA) in 2010, further trials are under way to determine the optimal role for bronchial thermoplasty in asthma management as we move forward.

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FIGURE 14.8 Bronchial thermoplasty. Arrow points to thermal energy element.

Nonpharmacologic Interventions in the Treatment of Asthma

In addition to the pharmacologic interventions used to manage asthma, a number of other therapies may be helpful in the control of asthma and/or reducing future exacerbation risks. Box 14.4 provides an overview of common nonpharmacologic interventions.

Box 14.4

Nonpharmacologic Interventions Commonly Used to Manage Asthma

Smoking cessation

Physical activity

Avoidance of occupational exposures

Avoidance of medications that make asthma worse (e.g., aspirin and NSAIDs)

Healthy diet

Avoidance of indoor allergens (e.g., mold, dust mites, and/or pets)

Allergen immunotherapy

Weight reduction in obese patients

Breathing exercises

Avoidance of indoor air pollution

Avoidance of outdoor pollution

Encourage influenza vaccinations

Bronchial thermoplasty

Encourage strategies to deal with emotional stress

Avoidance of certain foods and chemicals

Indications for Referral for Expert Evaluation

Although most patients with asthma usually can be controlled in primary care, some clinical circumstances justify the referral for expert advice regarding the diagnosis and/or management of asthma. Box 14.5 shows common indications for considering referral for expert advice when possible.

Box 14.5

Indications for Considering Referral for Expert Advice

Difficulty confirming the diagnosis of asthma

Suspected occupational asthma

Persistent uncontrolled asthma or frequent exacerbations

Any risk factors for asthma-related death

Evidence of, or risk for, significant treatment side effects

Symptoms suggesting complications or subtypes of asthma (e.g., aspirin-exacerbated asthma)

See recommendations presented in Step 5, page 232.

Protocol When Asthma Is Controlled

When asthma control has been achieved, regular and ongoing monitoring of the patient's symptom control, risk factors, occurrence of exacerbations, and documentation of responses to any treatment changes is essential to maintain control and determine the lowest step and dose of treatment, which minimizes cost and maximizes the safety of treatment. It is also important to establish the patient's adherence with medications and other advice and any factors that contribute to poor adherence. It is also essential to ensure the patient has a full understanding of all asthma information associated with the patient's condition.

In addition, it should be confirmed that the patient is adequately trained in guided asthma self-management. Guided self-

management may involve varying degrees of independence ranging from patient-directed self-management to doctordirected self-management. With a doctor-directed self-management plan, the patient has a written action plan but contacts the doctor for most major treatment decisions. With a patient-directed self-management plan, the patient makes changes in accordance with a prior written action plan without needing to first contact the physician. A popular monitoring system is the asthma action plan, using green, yellow, and red zones (Fig. 14.9).

FIGURE 14.9 Asthma action plan. (Courtesy Dayton Children's Hospital Dayton, Ohio.)

Even when the asthma action plan is appropriately designed, the full benefit of any treatment changes may be evident only after 3 to 4 months. It may take much longer in severe cases. Stepping up asthma treatment can be done in the following three ways: (1) sustained step up (which is designed for 2 to 3 months), (2) short-term step up (which is for 1 to 2 weeks), or (3) day-to-day adjustments. Stepping down treatment may, or should, be considered once good asthma control has been achieved and maintained for 3 months, and lung function has reached a plateau.

The primary goals of stepping down are to find the minimum effective treatment and encourage patients to continue regular controller treatment on their own. Guided asthma self-management education and skills training include:

Skills training for effective use of inhaler devices

Patient adherence with medications and related advice

Asthma information

Training in guided asthma self-management—for example, self-monitoring of symptoms and/or peak flow, written action plan, and regular review of asthma control, treatment, and skills by a health care provider.

Although the majority of asthma symptoms usually can be managed in primary care, some patients warrant referral for expert advice. Indications for considering a referral for an expert opinion include the following:

Difficulty confirming the diagnosis of asthma

Suspected occupational asthma

Persistent uncontrolled asthma or frequent exacerbations

Any risk factors for asthma-related death

Evidence of, or risk for, significant treatment side effects

Symptoms suggesting complications or subtypes of asthma

Management of Asthma Exacerbation

An asthma exacerbation (also called an asthma attack or asthma episode) is characterized by a progressive increase in symptoms of shortness of breath, cough, wheezing or chest tightness, and progressive decrease in lung function (e.g.,

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decreased PEFR or FEV1). Exacerbations may occur in patients with a preexisting diagnosis of asthma or, in some cases, as

the first presentation of asthma. Exacerbations most often occur after the patient has been exposed to an external agent (e.g., viral upper respiratory tract infection, pollen, or pollution) and/or poor adherence with controller medications. Severe exacerbations may occur in patients with mild to well-controlled asthma. Table 14.4 provides a clinical scale to classify the severity of asthma exacerbations. Severe asthma exacerbations are potentially life threatening, and their monitoring and treatment require close supervision. Fig. 14.10 provides an overview of GINA's recommended management of asthma exacerbations in primary care in adults, adolescents, and children 6 to 11 years. Fig. 14.11 shows an overview of GINA's management of asthma exacerbations in an acute care facility (e.g., emergency department).

TABLE 14.4

Classification of Severity of Acute Asthma Exacerbations*

 

Mild

Moderate

Severe

Respiratory Arrest

 

Imminent

 

 

 

 

Symptoms

 

 

 

 

Breathlessness

While walking

While talking (infant:

While at rest (infant:

 

 

 

softer, shorter cry;

stops feeding)

 

 

 

difficulty feeding)

 

 

 

Can lie down

Prefers sitting

Sits upright

 

Talks in

Sentences

Phrases

Words

 

Alertness

May be agitated

Usually agitated

Usually agitated

Drowsy or confused

Signs

 

 

 

 

Respiratory rate

Increased

Increased

Often >30/min

 

 

 

Normal rates of breathing in awake children:

 

 

 

Age

Normal Rate

 

 

 

<2 mo

<60/min

 

 

 

2–12 mo

<50/min

 

 

 

1–5 yr

<40/min

 

 

 

6–8 yr

<30/min

 

Use of accessory

Usually not

Commonly

Usually

Paradoxical

muscles;

 

 

 

thoracoabdominal

suprasternal

 

 

 

movement

retractions

 

 

 

 

Wheeze

Moderate, often

Loud; throughout

Usually loud; throughout

Absence of wheeze

 

only end-

exhalation

inhalation and

 

 

expiratory

 

exhalation

 

 

 

Normal pulse rates in awake children:

 

Pulse/min

<100

100–120

>120

Bradycardia

 

 

Age

Normal Rate

 

 

 

2–12 mo

<160/min

 

 

 

1–2 yr

<120/min

 

 

 

2–8 yr

<110/min

 

Pulsus paradoxus

Absent

May be present 10–

Often present >25 mm Hg

Absence suggests

 

<10 mm Hg

25 mm Hg

(adult) 20–40 mm Hg

respiratory

 

 

 

(child)

muscle fatigue

Functional Assessment

 

 

 

PEFR (% predicted or

80%

~50%–80%

<50% predicted or

 

% personal best)

 

 

personal best or

 

 

 

 

response lasts <2 h

 

PaO2 (on air)

Normal (ABG

>60 mm Hg (ABG usually

<60 mm Hg: possible

 

 

usually

necessary)

cyanosis

 

 

necessary)

 

 

 

and/or

 

 

 

 

PaCO2

<42 mm Hg

<42 mm Hg (ABG usually

≥42 mm Hg: possible

 

 

(ABG usually

necessary)

respiratory failure

 

 

necessary)

 

 

 

SaO2 % (on air) at sea

>95% (ABG

91%–95%

<91%

 

level

usually

 

 

 

 

necessary)

 

 

 

 

 

 

 

 

 

Hypercapnia (hypoventilation) develops more readily in young children than in adults and

 

adolescents

 

 

 

*The presence of several findings, but not necessarily all, suggests the general classification of the exacerbation. Many of these parameters have not been systematically studied, so they serve only as general guides. From Expert Panel Response 3 (EPR 3): Guidelines for the diagnosis and management of asthma, 2007 (http://www.nhlbi.nih.gov/guidelines/asthma/asthgdln.htm).

PEFR, Peak expiratory flow rate.

FIGURE 14.10 Management of asthma exacerbations in primary care (adults, adolescents, children 6 to 11 years). (Modified from Global Strategy for Asthma Management and Prevention, 2017, GINA. http://www.ginasthma.org.)

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FIGURE 14.11 Management of asthma exacerbations in acute care facility (e.g., emergency department). (Modified from Global Strategy for Asthma Management and Prevention, 2017, GINA. http://www.ginasthma.org.)

Management of Asthma With Comorbidities and Special Populations

Several comorbidities are often associated with asthma, especially those with difficult-to-treat asthma or severe asthma. When possible, the treating of comorbidities is strongly recommended because they often contribute to the patient's symptoms. Common comorbidities associated with asthma include the following:

Obesity: Asthma is more difficult to control in obese patients. Weight loss in the obese patient improves asthma control and lung function and reduces medication needs.

Gastroesophageal reflux disease (GERD): Significant evidence indicates that gastroesophageal reflux is more common in patients with asthma and obstructive sleep apnea than the general population.

Anxiety and depression: Psychiatric disorders, especially depressive and anxiety disorders, are common among people with asthma.

Food allergy and anaphylaxis: Although food allergy as a trigger for asthma symptoms is rare (less than 2% of people with asthma), in patients with confirmed food-induced allergic reaction (anaphylaxis), coexisting asthma is a strong risk factor for more severe and even fatal reactions. Food-induced anaphylaxis often presents as life-threatening asthma.

Rhinitis, sinusitis, and nasal polyps: Most patients with asthma, either allergic or nonallergic, have rhinitis. Upper airway disease often adversely influences airway function in some patients with asthma.