Skip Navigation LinksHome > May 2011 - Volume 114 - Issue 5 > Case Scenario: Bronchospasm during Anesthetic Induction
Anesthesiology:
doi: 10.1097/ALN.0b013e3182172cd3
Education: Case Scenario

Case Scenario: Bronchospasm during Anesthetic Induction

Dewachter, Pascale M.D., Ph.D.*; Mouton-Faivre, Claudie M.D.†; Emala, Charles W. M.D.‡; Beloucif, Sadek M.D., Ph.D.§
Section Editor(s): Riou, Bruno M.D., Ph.D., Editor

Free Access
Continued Medical Education
Article Outline
Collapse Box

Author Information

BRONCHOSPASM, the clinical feature of exacerbated underlying airway hyperreactivity, has the potential to become an anesthetic disaster. During the perioperative period, bronchospasm usually arises during induction of anesthesia but may also be detected at any stage of the anesthetic course. Accordingly, prompt recognition and appropriate treatment are crucial for an uneventful patient outcome. Perioperative bronchospasm (i.e., the clinical expression of exacerbated underlying airway reactivity) may be associated with type E immunoglobulin (IgE)-mediated anaphylaxis or may occur as an independent clinical entity, triggered by either mechanical and/or pharmacologic factors. Whatever the clinical circumstances, different triggers are identified in the occurrence of perioperative bronchospasm with asthma, a chronic inflammatory disorder of the airways frequently involved. The purpose of this clinical scenario is to discuss the key points of perioperative bronchospasm.
Back to Top | Article Outline

Case Report

A 25-yr-old woman with morbid obesity (body mass index: 54 kg/m2) and noninsulin-dependent diabetes was scheduled for cochlear implant surgery. She had two previous surgeries without incident during childhood. She denied any history of atopy or drug allergy. Chest auscultation was normal before anesthesia. She was premedicated with hydroxyzine (100 mg orally) the day before and 1 h before anesthesia, which was induced with sufentanil (20 μg intravenously) and propofol (350 mg intravenously). Tracheal intubation (Cormack and Lehane grade I) was facilitated with succinylcholine (130 mg intravenously). After tracheal intubation was performed, chest auscultation revealed a complete absence of bilateral breath sounds. Initial concentrations of end-tidal carbon dioxide (ETco2) were low. Because an esophageal intubation was suspected, the patient was immediately extubated and mask ventilation attempted. Mask ventilation was difficult to perform because of dramatically decreased lung compliance, whereas ETco2 demonstrated a marked prolonged expiratory upstroke of the capnogram. Therefore, bronchospasm was considered. Rapid arterial oxygen desaturation (oxygen saturation measured by pulse oximetry [Spo2], 55%) followed by arterial hypotension (from 130/75 to 50/20 mmHg) associated with a moderate tachycardia (100 beats/min) occurred in less than 5 min after the onset of bronchospasm. Concomitantly, titrated epinephrine (two intravenous boluses of 100 μg each) along with fluid therapy with crystalloids (lactated Ringer's solution, 1,000 ml) corrected the cardiovascular disturbances (arterial blood pressure, 110/50 mmHg; heart rate, 110 beats/min) while at the same time ventilation became easier to perform along with the return of audible wheezing over both lung fields. As arterial blood pressure was restored, a localized (face and upper thorax) erythema occurred. Hydrocortisone (200 mg) was intravenously administered. A blood sample was obtained to measure serum tryptase concentrations, 40 and 90 min after the clinical reaction. Surgery was postponed, and the patient was transferred to the intensive care unit. No additional supportive vasopressor therapy was required. Respiratory symptoms resolved within 2 h after inhaled β2-agonist (salbutamol; i.e., albuterol) and intravenous corticoids (hydrocortisone, cumulative dose: 800 mg over 24 h). Subsequent clinical outcome was uneventful, and the patient was discharged home the following day and returned 6 weeks later for allergologic assessment (see section III).
Back to Top | Article Outline

Discussion

I. Diagnosis and Differential Diagnosis of Intraoperative Wheezing/Bronchospasm
Bronchospasm encountered during the perioperative period and especially after induction/intubation may involve an immediate hypersensitivity reaction including IgE-mediated anaphylaxis or a nonallergic mechanism triggered by factors such as mechanical (i.e., intubation-induced bronchospasm) or pharmacologic-induced (via histamine-releasing drugs such as atracurium or mivacurium) bronchoconstriction in patients with uncontrolled underlying airway hyperreactivity.1,2 Chest auscultation should be done to confirm wheezing, whereas decreased or absent breath sounds suggest critically low airflow.3 The differential diagnosis includes inadequate anesthesia, mucous plugging of the airway, esophageal intubation, kinked or obstructed tube/circuit, and pulmonary aspiration.3 Unilateral wheezing suggests endobronchial intubation or an obstructed tube by a foreign body (such as a tooth).3 If the clinical symptoms fail to resolve despite appropriate therapy, other etiologies such as pulmonary edema or pneumothorax should also be considered.
Back to Top | Article Outline
II. Diagnosis of a Perioperative Immediate Reaction
Immediate hypersensitivity is a clinical entity evoking allergy that varies in severity1 and is subdivided into nonallergic hypersensitivity (called anaphylactoid reaction by the American Academy of Allergy Asthma and Immunology) where an immune mechanism is excluded, and allergic hypersensitivity (also called IgE-mediated anaphylaxis).4 By definition, immediate hypersensitivity occurs within 60 min after the injection/introduction of the culprit agent.1 The initial diagnosis remains presumptive, whereas the etiologic diagnosis is linked to a triad including clinical features (the description of the clinical features according to the adapted Ring and Messmer clinical severity scale); blood tests (tryptase level measurements, serum-specific IgEs); and postoperative skin tests with the suspected drugs or agents.1
Back to Top | Article Outline
III. Etiology of This Perioperative Immediate Hypersensitivity in the Current Case
The sudden occurrence of bronchospasm after anesthetic induction, with cardiovascular disturbances and cutaneous signs, clinically suggested a drug-induced anaphylactic reaction. Succinylcholine-induced anaphylaxis was the most likely etiology, because neuromuscular blocking agents are the most frequent agents involved in perioperative anaphylaxis in adults.1,5 Skin testing remained negative in response to propofol, sufentanil, succinylcholine, and latex solutions (Allerbio, Varennes en Argonne, France and Stallergènes, Antony, France). Tryptase levels (ImmunoCAP, Phadia SAS, Uppsala, Sweden) were unchanged (5.4 μg · l−1 and 4.3 μg · l−1; N less than 13.5 μg · l−1) in blood samples obtained 40 and 90 min, respectively, after the onset of the reaction. Serum-specific IgEs (ImmunoCAP) against succinylcholine and latex were not detectable. Specific serum IgE against quaternary ammonium was slightly increased (2.08 kU/L, N less than 0.1). A basophil activation test was also performed and analyzed using a FACSCanto II flow cytometer (Becton-Dickinson, Rungis, France). Succinylcholine induced neither CD63 nor CD203c up-regulation.
Back to Top | Article Outline
Clinical Considerations.
The chronology of evolving clinical features is crucial to understand the pathophysiologic mechanism of an immediate hypersensitivity reaction.
Cardiovascular disturbance is the hallmark of severe IgE-mediated anaphylaxis. In patients with neuromuscular blocking agent-induced perioperative anaphylaxis, cardiovascular signs are usually the inaugural clinical event and occur within minutes after the drug challenge. These cardiovascular signs may be associated with or followed by bronchospasm in 19–40% of patients, more likely in those with underlying asthma or chronic obstructive pulmonary disease.1 Drug-induced anaphylactic bronchospasm may occur either before or after instrumentation of the airway2 (fig. 1).
Latex-induced anaphylaxis typically occurs in patients with a history of atopy.6 Because atopy is the strongest identifiable predisposing factor for the development of asthma,7 severe clinical features occurring during latex-induced anaphylaxis usually involve cardiovascular signs followed by or associated with bronchospasm and cutaneous signs.8 As latex proteins are slowly absorbed, latex-induced anaphylaxis usually occurs up to 30–60 min after the beginning of surgery (i.e., mucous membrane exposure).8
Acute increases in airway responsiveness may also occur in the absence of an antigen challenge and result from irritation of the well-innervated upper airway by a foreign body (e.g., endotracheal tube or suction catheter).2 Thus, nonallergic bronchospasm immediately follows nonspecific stimuli and usually is not associated with cardiovascular symptoms2 (fig. 1). Nevertheless, positive end-expiratory pressure with severe bronchospasm may lead to a decrease in venous return and hence of cardiac output. In addition, the association of hypoxia and respiratory failure from inadequate ventilation may lead to cardiovascular collapse.9
Back to Top | Article Outline
IV. Distinguishing the Pathophysiologic Mechanism of Perioperative Bronchospasm Clinically
Four clinical variables were identified as independent predictors of allergic compared with nonallergic perioperative bronchospasm: the presence of any cutaneous symptoms; shock; episodes of desaturation; and the prolonged duration of clinical features (longer than 60 min).2 Compared with that of patients who did not present with these “predictive” signs as part of the clinical syndrome, the occurrence of hypotension or episodes of oxygen desaturation were 27 and 21 times, respectively, more likely to be associated with IgE-mediated anaphylaxis. In addition, symptom duration longer than 60 min or the presence of skin changes was two and seven times, respectively, more likely to be associated with IgE-mediated anaphylaxis.2 In the current case, inaugural severe bronchospasm triggered by endotracheal tube insertion and followed by cardiovascular collapse, likely related to subsequent hypoxemia after the patient's extubation, yields clinical insight into the pathophysiologic mechanism of the reaction and suggests nonallergic bronchospasm. Cutaneous signs, such as erythema, are not specific for IgE-mediated anaphylaxis per se and may also be observed during nonallergic bronchospasm.2 The morbid obesity of the patient is of clinical interest and could also have been a precipitating factor of rapid arterial desaturation despite appropriate preoxygenation.
Back to Top | Article Outline
Allergologic Assessment: Blood Tests and Skin Testing.
A tryptase increase is specific for mast cell activation such as that occurring during IgE-mediated anaphylaxis.1 Increased tryptase levels appear to distinguish clearly between allergic and nonallergic perioperative bronchospasm.2 Thus, Fisher2 suggested that an allergologic assessment is unnecessary in patients with isolated bronchospasm occurring after airway instrumentation without an increase in tryptase. In the current case, allergic mast cell activation was ruled out because tryptase levels measured within the recommended time frame remained unchanged. Skin tests were negative in response to the medications received (i.e., propofol, sufentanil, and succinylcholine) as well as latex. These results were corroborated by basophil activation tests showing an absence of CD63 and CD203c up-regulation with succinylcholine, ruling out basophil sensitization by specific IgE toward succinylcholine and undetectable specific serum IgEs against succinylcholine. Serum IgEs against quaternary ammonium was slightly increased (2.08 kU/L, N less than 0.1), but these assays appear to be less sensitive than skin tests and do not prove that the drug/agent is responsible for the reaction.10
Succinylcholine-induced anaphylaxis was therefore ruled out according to clinical, biologic, and allergologic evidence. This is of particular importance because succinylcholine is thereby allowed to be used for future anesthetics in this patient. In turn, uncontrolled asthma was suggested to be the main trigger of this nonallergic bronchospasm after endotracheal tube insertion. Wheezing induced by bronchial infection during childhood or triggered by cold weather and exercise in adulthood was elicited from the patient's history during the postoperative evaluation.
Back to Top | Article Outline
V. Asthma Is a Frequently Underdiagnosed Condition
Asthma is one of the most common chronic airway diseases worldwide, with a higher prevalence and incidence in the Western world.11 The estimated annual death rate worldwide is 250,000.12 However, this condition frequently remains underdiagnosed. In 2008, the following definition for asthma was suggested: “Asthma is a chronic disorder of the airway in which many cells and cellular elements play a role. The chronic inflammation is associated with airway responsiveness that leads to recurrent episodes of wheezing, breathlessness, chest tightness and coughing, particularly at night or in the early morning. These episodes are usually associated with widespread, but variable airflow obstruction within the lung, that is often reversible either spontaneously or with treatment.”12 This proposal was ratified in the United States.7 Accordingly, a European and American Task Force issued by the corresponding Respiratory Societies suggested that the definition of asthma includes two domains (symptoms and variable airway obstruction) being assessed in clinical practice, with two additional domains (airway inflammation and hyperresponsiveness) characterizing the underlying disease. An individual may have features of any or all of these domains.13 Airway hyperresponsiveness is induced by a variety of changes in the airway and sustained by underlying airway inflammation, the hallmark of asthma.
Recently, a crucial modification in the approach to asthma management was proposed with a classification by the level of asthma control (controlled, partly controlled, or uncontrolled) rather than asthma severity per se while linking the classification of asthma control to asthma treatment.12
Back to Top | Article Outline
Two Main Phenotypes of Asthma Can be Distinguished.
Two main phenotypes of asthma, allergic and nonallergic, are most commonly discussed; overlap may occur within these groups.14
Back to Top | Article Outline
Allergic Asthma.
The largest overall phenotype in children and adults is allergic asthma. Although allergic asthma is a chronic and often lifelong disease, its onset occurs primarily in early childhood. However, more than 50% of asthma is allergic in adults.4 It results from immunologic reactions, mostly initiated by IgE antibodies, and is also called IgE-mediated allergic asthma. Genetic factors may promote the development of allergic asthma (inheritable component). Environmental factors such as tobacco smoke, air pollutants, and exposure to allergens including indoor (mites, animals, plant origin, e.g., ficus), outdoor (pollens, molds) or occupational allergens may trigger asthma. Obesity, diet, and a hygiene hypothesis may also trigger asthma.11 Thus, any potential risk factor must eventually interact with an underlying genetically determined pathway to result in the manifestation of disease (epigenetic component). However, atopy, the genetic predisposition for the development of an IgE-mediated response to common aeroallergens, is the strongest identifiable predisposing factor for developing asthma.7 Two major factors such as airborne allergens and viral respiratory infections seem to be the most important in the development, persistence, and possibly the severity of allergic asthma.7
Back to Top | Article Outline
Allergic Rhinitis and Allergic Asthma Belong to the Same Airway Disease.
The effect of allergic rhinitis on asthma should also be highlighted15 because the link of this disturbance with asthma remains poorly understood. Rhinitis is characterized by nasal symptoms including sneezing, nasal blockage, and/or itching of the nose; is either intermittent or permanent; and is classified as mild, moderate, or severe.15 More than 80% of asthmatic individuals have rhinitis, and 10–40% of patients with rhinitis have asthma. A combined strategy should ideally be used to treat the upper and lower airway diseases (allergen avoidance is crucial but inhaled/intranasal corticosteroid is the most consistently effective long-term control therapy attenuating airway inflammation). 7,15 Because the presence of asthma must be considered in all patients with rhinitis, those with severe and/or persistent uncontrolled allergic rhinitis should be evaluated for asthma before surgery.
Back to Top | Article Outline
Nonallergic Asthma: Aspirin-induced Asthma.
The other main variant of asthma in adults includes a widely underdiagnosed phenotype not seen in childhood, such as aspirin-induced asthma. Aspirin-induced asthma is characterized by eosinophilic rhinosinusitis, nasal polyposis, aspirin or nonsteroidal antiinflammatory drug sensitivity, and asthma. Asthma and sensitivity to aspirin usually appear approximately 1–5 yr after the onset of rhinitis,16 whereas rhinorrhea, nasal congestion, and anosmia are usually the first clinical features of aspirin-induced asthma. This phenotype results from the inhibition of cyclooxygenase enzymes by aspirin-like drugs in the airway of sensitive patients and is not sustained by an allergic mechanism.16
Back to Top | Article Outline
VI. Perioperative Bronchospasm
Asthma is considered to be more prevalent in westernized countries.11 Surprisingly, no academic society of anesthesiology issued from the European or the North American continents has published recommendations concerning the perioperative management of the asthmatic patient. The literature on this topic remains scarce.
Back to Top | Article Outline
Epidemiology of Perioperative Bronchospasm.
The occurrence of perioperative bronchospasm has been reported in up to 9% of asthmatic patients given general anesthesia, mainly after endotracheal tube insertion.17 Smoking also represents a major risk. Compared with that of nonsmokers, the relative risk of perioperative bronchospasm in smokers appears higher in females and in young smokers (16–39 yrs old) and is higher in patients with chronic bronchitis than in asymptomatic patients.18
Back to Top | Article Outline
Why and When Does Perioperative Bronchospasm Occur?
Of the 4,000 incidents reported in Australia, 103 reports of perioperative bronchospasm (3%) showed that an allergic mechanism was less frequently involved (21%) than a nonallergic mechanism (79%).19 Among these nonallergic cases, 44% occurred during the induction of anesthesia, 36% during the maintenance phase, and 20% during the emergence/recovery stage. During induction of anesthesia, bronchospasm was mainly related to airway irritation (64%), whereas remaining causes were due to tube misplacement (17%), aspiration (11%), and other pulmonary edema or unknown causes (8%). During the maintenance stage of anesthesia, allergy (34%), endotracheal tube malposition (23%), airway irritation (11%), and aspiration with a laryngeal mask airway (9%) together accounted for almost 80% of the occurrences of bronchospasm. During induction or maintenance of anesthesia, bronchospasm caused by airway irritation occurred more frequently in patients who had one or more predisposing factors such as asthma, heavy smoking, or bronchitis. Others showed that an allergic mechanism accounted for 60% of the cases in patients experiencing bronchospasm during induction of anesthesia.2 A previous history of asthma was present in 50% and 60% of patients with nonallergic and allergic bronchospasm, respectively. Thus, uncontrolled asthma/chronic obstructive pulmonary disease is frequently involved with either pathophysiologic mechanisms (allergic vs. nonallergic), regardless of the stage of anesthesia (induction or maintenance).
Back to Top | Article Outline
Morbidity and Mortality Rates.
Respiratory events accounted for 28% of claims concerning anesthesia-related brain damage and death in the United States.20 In this series, bronchospasm was included in the other categories and together corresponded to 11% of total respiratory events. In the United Kingdom, respiratory and airway incidents accounted for 3% and 8%, respectively, of all claims including severe and fatal outcomes.21 Bronchospasm was not detailed. Nevertheless, airway incidents belong to the claims with the highest overall cost and respiratory complications with the highest mean cost per closed claim. Seven percent of anesthesia-related deaths were attributed to bronchospasm in France.22
In conclusion, bronchospasm remains a serious life-threatening perioperative event. Its dramatic consequences involving brain damage or death may be partly explained by substandard care and/or inadequate practice and system failures.20,22 Optimal management of perioperative bronchospasm should therefore be encouraged through teaching applications such as an anesthesia simulator to compensate for the low frequency with which the average practitioner would encounter severe bronchospasm during routine clinical care.
Back to Top | Article Outline
Basic Science: Mechanisms of Reflex-induced Bronchoconstriction.
The mechanisms of asthmatic exacerbations resulting in bronchoconstriction are complex and involve airway nerves, smooth muscle, epithelium, and inflammatory cells. However, reflex-induced bronchoconstriction induced by irritation of the upper airway by a foreign body such as an endotracheal tube is modulated by synapse of afferent sensory pathways in the nucleus of the solitary tract, which projects to the airway-related vagal preganglionic neurons. The excitatory neurotransmitter glutamate modulates stimulation of the nucleus of the solitary tract and airway-related vagal preganglionic neurons, whereas inhibitory nerves releasing γ-aminobutyric acid project from the nucleus of the solitary tract to the airway-related vagal preganglionic neurons.23 The excitatory outflow from the airway-related vagal preganglionic neurons back to the airway is carried in the vagus nerve and results in acetylcholine release onto airway structures, most prominently the M3 muscarinic receptor on airway smooth muscle that induces airway constriction.24 Thus, the initial airway irritant stimulus sends an afferent signal to the brainstem, resulting in an efferent signal traveling in the vagus and releasing acetylcholine in the airway (fig. 2). Because acetylcholine acting on M3 muscarinic receptors on airway smooth muscle is a key mechanistic component of reflex-induced bronchoconstriction, the use of antimuscarinic-inhaled medications (e.g., ipratropium or tiotropium) should be advantageous to prevent or treat this phenomenon.25 In addition, nonadrenergic noncholinergic nerves releasing tachykinins, vasoactive intestinal peptide, and calcitonin gene-related peptide may participate in this reflex arc and/or locally release the procontractile neurotransmitters via activation of interneurons in the airway.26 A recent study suggests that propofol preferentially relaxes tachykinin-induced airway constriction in airway smooth muscle.27 It has long been clinically recognized that the depth of anesthesia modulates the likelihood of eliciting reflex-induced bronchoconstriction, but the pharmacologic mechanisms by which this occurs are unknown. Propofol28 and the volatile inhalational anesthetics (with the exception of desflurane) are known to be clinically effective at preventing reflex-induced bronchoconstriction or attenuating intraoperative bronchoconstriction.29 These agents share activity at inhibitory γ-aminobutyric acid-A chloride channels30; thus, it has been speculated that modulation of γ-aminobutyric acid input to the airway-related vagal preganglionic neurons from the nucleus of the solitary tract and higher central nervous system centers may be a mechanism by which deepening anesthesia prevents or relieves reflex-induced bronchoconstriction. Moreover, both propofol and inhalational anesthetics have direct bronchodilatory effects at the level of airway smooth muscle itself31 acting via γ-aminobutyric acid-A channels32 or modulating calcium sensitivity of the contractile proteins.33 However, despite these protective effects of intravenous propofol and the adequate induction dose used in the current case, reflex-induced bronchoconstriction developed in this patient who had previously unrecognized and untreated asthma.
Back to Top | Article Outline
VII. Obesity and Asthma: Is There Any Relationship?
There is increasing evidence linking obesity, defined as a body mass index of at least 30 kg/m2, to asthma and airway hyperreactivity in both children and adults.34 Both asthma and obesity are systemic inflammatory states. Their development seems to be determined early in life, with this association not being mediated through atopy.34 In turn, potential explanations for the parallel increase of asthma and obesity might involve genetic, mechanical, hormonal, and environmental factors. Accordingly, chromosomal regions with loci common to obesity and asthma phenotypes have been identified. Reduced functional residual capacity and decreased tidal volume as a result of obesity result in greater contractile responses of airway smooth muscle, causing potentially increased airway reactivity.34–35 Although gastroesophageal reflux resulting from obesity may potentially trigger a latent asthmatic condition,11 this condition was ruled out with an esophageal transit test.
Hormonal influences may also be involved as the effect of obesity on asthma is stronger in females than males.35 In addition, the hormone leptin produced by adipocytes and that acts in the hypothalamus to signal satiety35 has effects on immune cell function and inflammation. Serum leptin levels in adulthood were shown to be higher in women than men with a higher prevalence of asthma.34 The association between asthma and obesity may be of recent origin, suggesting that recent changes in lifestyle and diet are now associated with both asthma and obesity.11 However, weight gain antedates asthma or asthma symptoms, ruling out the hypothesis that this association might be the result of reduced physical activity by asthmatic patients leading to obesity.34
Back to Top | Article Outline
VIII. Sleep-disordered Breathing and Asthma
Sleep-disordered breathing is more prevalent in asthmatic individuals than in those without asthma, whereas sleep-disordered breathing and asthma share common risk factors such as obesity.35 The reasons for the association between both conditions remain unknown.35 Asthma remains underdiagnosed in obese patients because respiratory symptoms are frequently attributed to being overweight, as was the case in our patient. In such patients, underlying airway hyperreactivity should be cautiously assessed during the preoperative evaluation (see section IX).
In the current case and after the clinical postanesthetic evaluation, borderline sleep-disordered breathing was also detected through polysomnography.
Back to Top | Article Outline
IX. Prevention of Perioperative Bronchospasm
The controls of airway inflammation and corresponding asthma symptoms are essential to optimize perioperative and postoperative care. The National Asthma Education and Prevention Program Expert Panel Report 3 recommends that the level of asthma control, medication use (especially oral systemic corticosteroid within the past 6 months), and pulmonary function be reviewed before surgery.7 The Global Initiative for Asthma guidelines suggest that perioperative and postoperative complications rely on the severity of asthma at the time of surgery, the type of surgery (thoracic and upper abdominal surgeries being at increased risk), and modalities of anesthesia (general anesthesia with tracheal intubation is at higher risk).12 Others suggest that uncontrolled or poorly controlled asthma may be assessed through the degree of asthma control (increased use of inhaled short-acting β2-agonists, previous/current use of inhaled corticosteroids, recent use of oral/injected corticosteroids, recent exacerbations of asthma symptoms, emergency department or hospital visit within the last months) and potential risks or complication factors (recent infection of the respiratory tract, previous bronchospasm after intubation, pulmonary complications during/after previous surgical procedure, long-term use of a systemic corticosteroid for severe asthma, associated gastroesophageal reflux or smoking).36 The common key point of these recommendations focuses on the level of asthma control before surgery7,12,36 as uncontrolled asthma is considered to be the main risk factor for bronchoconstriction during surgery.36
Back to Top | Article Outline
Preoperative Clinical and Physical Examination.
Careful clinical and physical examinations are therefore crucial for preoperative pulmonary risk assessment to identify findings suggestive of unrecognized underlying airway hyperreactivity. Decreased breath sounds as seen in markedly decreased expiratory airflow, sibilants, rhonchi, and prolonged expiratory phase, as well as recent and/or frequent exacerbations of respiratory symptoms including wheezing, cough, exercise intolerance, unexplained dyspnea, and gastroesophageal reflux disease should raise concern during the preoperative evaluation.3 Among these different findings, decreased breath sounds, dullness to percussion, wheezing, rhonchi, and a prolonged expiratory phase predict an increase in the risk of perioperative pulmonary complications.37 Thus, poorly controlled asthma usually favors perioperative pulmonary complications3,36,38 whereas airway instrumentation may induce life-threatening bronchospasm, perioperative complications, and prolonged intensive care treatment.20 Conversely, controlled asthma does not promote additional risk.36,38
Back to Top | Article Outline
Corticosteroids Are the Key Point of Antiasthma Long-term Control Therapy.
Long-term therapy is used daily to achieve and maintain asthma control. Asthma is an inflammatory condition. Thus, inhaled glucocorticosteroids are currently the most effective antiinflammatory drug for the treatment of persistent asthma.7,12 Glucocorticosteroids reduce asthma symptoms, improve lung function, decrease airway hyperreactivity, modulate airway inflammation, and reduce asthma exacerbations and asthma mortality.12 Inhaled long-acting β2-agonists (formoterol, salmeterol) should never be used as single therapy because these β2-agonists improve lung function without antiinflammatory effects.12 Thus, significant clinical concerns regarding an increase in asthma-related deaths in patients on long-acting β2-agonists39 have led to revisions of product labels by the United States Food and Drug Administration stating that long-acting β2-agonists should never be used without concomitant inhaled corticosteroid therapy.40 Thus, β2-agonists are most efficient when combined with glucocorticosteroids, when inhaled glucocorticosteroids alone fail to relieve asthma symptoms.7,12 Corticosteroids increase the bronchodilatory effect of β2-agonists and increase the number of β2-adrenergic receptors and their response to β2-agonists.41 In turn, rapid-acting inhaled β2-agonists are used for quick relief of acute asthma exacerbations.7,12 Additional studies are necessary to determine whether tiotropium and possibly other long-acting anticholinergic agents are effective and safe alternatives to long-acting β2-agonists for the long-term treatment of asthma.42
Back to Top | Article Outline
Preoperative Pulmonary Evaluation.
Table 1
Table 1
Image Tools
In the presence of active bronchospasm, elective surgery should be postponed. The cause and corresponding clinical symptoms should be actively treated until baseline status is achieved.3 Patients should be free of wheezing, cough, or dyspnea.38 Individuals having symptoms suggestive of asthma, outside the context of an emergency situation, should undergo preoperative assessment performed by pulmonologists to assess the degree of airway reactivity and optimize preoperative treatment. Measurement of lung function to prove airflow limitation and the demonstration of reversibility of lung function abnormalities enhance diagnostic confidence.12 Forced expiratory volume in 1 s (FEV1) or peak expiratory flow (PEF) are valid measures of airway caliber and better indicators of the severity of asthma exacerbation than clinical symptoms.7,12 FEV1 (normal is approximately 80–100% of predicted) expressed as a percentage of the vital capacity is the standard index for assessing and quantifying airflow limitation. Reversibility with the use of a bronchodilator is defined as an increase in FEV1 of at least 12% or 200 ml. FEV1/forced vital capacity (normal is greater than 75%) appears to be a more sensitive measure of severity and control.7 In turn, a peak flow meter, which measures the highest expiratory flow rate in liters of air expired per second or per min (normal is greater than 80% of predicted), is designed for monitoring due to the wide variability in reference values.7,12 Before surgery, PEF or FEV1 greater than 80% of the predicted or personal best is recommended.38 If PEF or FEV1 is less than 80%, a brief course of oral corticosteroids should be considered to reduce airflow limitation.12 Patients with asthma who are also smokers have poorer control of asthma.36 Abstinence from smoking before surgery reduces perioperative pulmonary complications rates. At least 2 months of preoperative cessation is required to drastically reduce perioperative pulmonary complications risk.38# A stepwise approach of either initiation or optimization of asthma treatment according to the level of asthma was proposed into either five12 or six steps7 reflecting increasing intensity of treatment required to achieve asthma control (table 1). Combined with educational and environmental measures, therapy for asthma is subdivided into two categories (quick-relief and long-term control treatment). Briefly, rapidly acting β2-agonist should be prescribed as needed at each step. The first step concerns patients with occasional daytime symptoms where rapid acting β2-agonist may be sometimes requested. The second through fifth steps concern a pattern of features involving partly controlled to severely uncontrolled asthma where regular treatment is requested. Low-dose inhaled corticosteroid is recommended for the second step. The combination of a low-dose inhaled corticosteroid with an inhaled long-acting β2-agonist or a medium- or high-dose inhaled corticosteroid with an inhaled long-acting β2-agonist is recommended for the third and fourth steps, respectively. Oral corticosteroids may be useful when added to other medications during the fifth step, which concerns patients with frequent exacerbations and daily limitation of activities.12 The recommendations proposed in the United States involve six steps but suggest a very similar therapeutic strategy (table 1). Therapy is increased as necessary and decreased when possible. In addition, some alternative drugs are also proposed. 7,12
A specific approach adapted to the preoperative stage, including emergency and nonemergency conditions, was proposed by a hospital-based working group.36 Thus, an international consensus promoted by the different corresponding anesthetic societies might be useful to define a better approach to airway hyperreactivity during the perioperative period.
In the current case, secondary pulmonary assessment confirmed uncontrolled allergic asthma (dust mites, grass). Initial spirometric evaluation showed a reduction of FEV1 and PEF at 67% and 70%, respectively, as well as an FEV1/forced vitality capacity of 83% of predicted values. High doses of inhaled therapy with fluticasone and salmeterol (1,000 μg, twice per day) along with educative measures were initiated. Three months later, a second spirometric evaluation showed bronchospasm reversibility of nearly 15%, with FEV1 at 80%, PEF at 82%, and an FEV1/forced vitality capacity of 97% of predicted values along with reduction of clinical signs noted by the patient as wheezing disappeared. These significant improvements have been noted at a constant body weight. Surgery was performed 6 months after the initial perioperative event. Anesthesia was conducted with propofol, sufentanil, and sevoflurane. Anesthesia and surgery as well as the postoperative course remained uneventful.
Back to Top | Article Outline
X. Treating Perioperative Bronchospasm
The aims of treatment are to relieve airflow obstruction and subsequent hypoxemia as quickly as possible.
Back to Top | Article Outline
General Measures.
When isolated perioperative bronchospasm occurs, oxygen concentration should be increased to 100%, and manual bag ventilation immediately started to evaluate pulmonary compliance and to identify all causes of high-circuit pressure.19 Increased concentration of a volatile anesthetic (sevoflurane, isoflurane) is often useful3 with the exception of desflurane because of its airway irritant effects, particularly in smokers.43 Deepening anesthesia with an intravenous anesthetic (propofol) may be required because intubation-induced bronchospasm may be related to an inadequate depth of anesthesia (fig. 3).
Back to Top | Article Outline
Inhaled Short-acting β2-Selective Agents Belong to Immediate Therapy.
Short-acting β2-selective agents (mainly using terbutaline and salbutamol) are key drugs for the fast relief of bronchoconstriction. Their onset of action occurs within 5 min, peak effect is within 60 min, and duration of action is 4–6 h. They should be immediately administered via a nebulizer (8–10 puffs to achieve appropriate therapeutic levels, may be repeated at 15- to 30-min intervals) or, if available, with a metered-dose inhaler (5–10 mg/h) connected to the inspiratory limb of the ventilator circuit. There is no difference in efficacy between terbutaline and salbutamol.** Continuous rather than intermittent administration of salbutamol results in greater improvement in PEF and FEV1. Moreover, nebulized epinephrine has no beneficial effect compared with terbutaline or salbutamol.**
Back to Top | Article Outline
Systemic Glucocorticosteroids Should Not be Omitted.
Parenteral steroids also remain a key drug in the treatment of bronchospasm because they speed resolution of exacerbations by decreasing airway inflammation. Systemic glucocorticosteroids such as methylprednisone (1 mg · kg−1) are preferred over cortisone because their antiinflammatory effect is more potent. However, the antiinflammatory benefit is not immediate.
Back to Top | Article Outline
Alternative Agents.
The use of an antimuscarinic inhaled medication (e.g., ipratropium bromide) has been shown to attenuate reflex-induced bronchoconstriction with efficacy similar to inhaled β2-agonists.25 Thus, combined nebulized ipratropium bromide (0.5 mg 4–6 times hourly) with a nebulized β2-agonist produces greater bronchodilatation than a β2-agonist alone and may be used to treat life-threatening bronchospasm or in those with a poor initial response to β2-agonist treatment.** Magnesium plays a beneficial role in the treatment of asthma through bronchial smooth muscle relaxation, leading to the use of intravenous (single dose of magnesium sulfate: 2 g over 20 min) or inhaled preparations (doses from 110 mg to 1,100 mg) in patients with severe bronchospasm that fails to be relieved with β2-agonists.12** Accordingly, salbutamol administered in isotonic magnesium sulfate provides greater benefit when compared with that diluted with saline.12 Intravenous aminophylline has no indication in acute bronchospasm because its use does not result in additional bronchodilatation, whereas adverse effects such as arrhythmia and vomiting have been reported when intravenous aminophylline was used.12**
Back to Top | Article Outline
Therapeutic Rationale for Epinephrine.
Epinephrine should be used in cases of associated cardiovascular collapse suggestive of IgE-mediated anaphylaxis.1,12 During isolated bronchospasm, its inhaled/systemic use is not recommended because no study has proven its efficiency when compared with β2-agonists such as salbutamol or terbutaline12 and deleterious adverse effects, including takotsubo cardiomyopathy, have been reported during asthma care.44 Others propose systemic epinephrine but emphasize that no advantage has been proven of systemic therapy over nebulization.7 Currently, no recommendations regarding epinephrine can be proposed,45 except that its use would be reasonable as a rescue therapy in patients with severe asthma complicated by hypotension that is not secondary to dynamic hyperinflation.46 Elective surgery should be postponed unless bronchospasm persists at baseline despite maximal medical optimization of the patient and further care provided in a monitored setting.
In our patient, extubation was performed because of suspected esophageal intubation. Verification of correct endotracheal tube position would have been the appropriate procedure. The patient's extubation was associated with oxygen arterial desaturation and subsequent hemodynamic disturbances.
Back to Top | Article Outline
XI. Knowledge Gap
Although factors contributing to airway inflammation in asthma are multiple and not completely understood, factors triggering perioperative bronchospasm are identified. Both basic science and clinical research efforts could improve the prevention and treatment of bronchospasm associated with anesthesia. Clinical research leading to the prevention of bronchospasm will require a better identification of patients at risk and then a better classification of the phenotypes, therapies, and level of control of asthma in patients during the preoperative period. Nevertheless, it should be questioned whether perioperative bronchospasm is a clinical entity of its own occurring in predisposed patients (e.g., asthmatic patients and those with chronic obstructive pulmonary disease or acute bronchitis) and triggered either by mechanical, pharmacologic, or inflammatory (i.e., anaphylaxis) factors. Moreover, basic assumptions regarding the management of general anesthesia in patients at risk for bronchoconstriction have not been rigorously studied, specifically the assumption that intubation of the trachea carries a higher risk of morbidity in the perioperative period compared with airway devices such as the laryngeal mask airway. Basic science advances are needed in the understanding of the interaction between anesthetics, airway irritation, and the role of tachykinins and other C fiber neurotransmitters in the control of airway tone. Moreover, the mechanisms by which intravenous and inhaled anesthetics affect airway nerves and directly modulate airway smooth muscle tone likely involve modulation of plasma membrane ion channels, membrane potential, and intracellular calcium sensitivity but remain poorly understood.
Table 2
Table 2
Image Tools
An international consensus promoted by the different corresponding anesthetic societies might be useful to define a better approach of airway hyperreactivity as well as provide key targeting questions to detect patients at risk during the preoperative period (table 2) and propose clinical pathways.
The authors thank Sylvie Chollet-Martin, Pharm.D., Ph.D., Unité d'Immunologie Auto-immunité & Hypersensibilités, Hôpital Bichat-Claude Bernard, Assistance Publique Hôpitaux de Paris & Université Paris-Sud 11, INSERM UMRS-996, ChÂtenay-Malabry, France, and Pascale Nicaise-Roland, Pharm.D., Ph.D., Staff Biologist, Unité d'Immunologie Auto-immunité & Hypersensibilités, Hôpital Bichat-Claude Bernard, Paris, France, for performing biologic assessment and Sylvie Bourdiau, M.D., Staff Anesthesiologist, Service d'Anesthésie-Réanimation, Dominique Valeyre, M.D., Service de Pneumologie, and Bruno Frachet, M.D., Service d'Oto-Rhino-Laryngologie, Hôpital Avicenne, Assistance Publique Hôpitaux de Paris, and Université Paris 13, Bobigny, France, for clinical management.
Back to Top | Article Outline

References

1. Dewachter P, Mouton-Faivre C, Emala CW: Anaphylaxis and anesthesia: Controversies and new insights. Anesthesiology 2009; 111:1141–50

2. Fisher MM, Ramakrishnan N, Doig G, Rose M, Baldo B: The investigation of bronchospasm during induction of anaesthesia. Acta Anaesthesiol Scand 2009; 53:1006–11

3. Woods BD, Sladen RN: Perioperative considerations for the patient with asthma and bronchospasm. Br J Anaesth 2009; 103(Suppl 1):i57–65

4. Johansson SG, Bieber T, Dahl R, Friedmann PS, Lanier BQ, Lockey RF, Motala C, Ortega Martell JA, Platts-Mills TA, Ring J, Thien F, Van Cauwenberge P, Williams HC: Revised nomenclature for allergy for global use: Report of the Nomenclature Review Committee of the World Allergy Organization, October 2003. J Allergy Clin Immunol 2004; 113:832–6

5. Hepner DL, Castells MC: Anaphylaxis during the perioperative period. Anesth Analg 2003; 97:1381–95

6. Sampathi V, Lerman J: Perioperative latex allergy in children. Anesthesiology 2011; 114:673–80

7. 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:S94–138

8. Hepner DL, Castells MC: Latex allergy: An update. Anesth Analg 2003; 96:1219–29

9. Hepner DL: Sudden bronchospasm on intubation: Latex anaphylaxis? J Clin Anesth 2000; 12:162–6

10. Harper NJ, Dixon T, Dugué P, Edgar DM, Fay A, Gooi HC, Herriot R, Hopkins P, Hunter JM, Mirakian R, Pumphrey RS, Seneviratne SL, Walls AF, Williams P, Wildsmith JA, Wood P, Nasser AS, Powell RK, Mirakhur R, Soar J: Working Party of the Association of Anaesthetists of Great Britain and Ireland: Suspected anaphylactic reactions associated with anaesthesia. Anaesthesia 2009; 64:199–211

11. Eder W, Ege MJ, von Mutius E: The asthma epidemic. N Engl J Med 2006; 355:2226–35

12. Bateman ED, Hurd SS, Barnes PJ, Bousquet J, Drazen JM, FitzGerald M, Gibson P, Ohta K, O'Byrne P, Pedersen SE, Pizzichini E, Sullivan SD, Wenzel SE, Zar HJ: Global strategy for asthma management and prevention: GINA executive summary. Eur Respir J 2008; 31:143–78

13. Taylor DR, Bateman ED, Boulet LP, Boushey HA, Busse WW, Casale TB, Chanez P, Enright PL, Gibson PG, de Jongste JC, Kerstjens HA, Lazarus SC, Levy ML, O'Byrne PM, Partridge MR, Pavord ID, Sears MR, Sterk PJ, Stoloff SW, Szefler SJ, Sullivan SD, Thomas MD, Wenzel SE, Reddel HK: A new perspective on concepts of asthma severity and control. Eur Respir J 2008; 32:545–54

14. Wenzel SE: Asthma: Defining of the persistent adult phenotypes. Lancet 2006; 368:804–13

15. Bousquet J, Khaltaev N, Cruz AA, Denburg J, Fokkens WJ, Togias A, Zuberbier T, Baena-Cagnani CE, Canonica GW, van Weel C, Agache I, Ait-Khaled N, Bachert C, Blaiss MS, Bonini S, Boulet LP, Bousquet PJ, Camargos P, Carlsen KH, Chen Y, Custovic A, Dahl R, Demoly P, Douagui H, Durham SR, van Wijk RG, Kalayci O, Kaliner MA, Kim YY, Kowalski ML, Kuna P, Le LT, Lemiere C, Li J, Lockey RF, Mavale-Manuel S, Meltzer EO, Mohammad Y, Mullol J, Naclerio R, O'Hehir RE, Ohta K, Ouedraogo S, Palkonen S, Papadopoulos N, Passalacqua G, Pawankar R, Popov TA, Rabe KF, Rosado-Pinto J, Scadding GK, Simons FE, Toskala E, Valovirta E, van Cauwenberge P, Wang DY, Wickman M, Yawn BP, Yorgancioglu A, Yusuf OM, Zar H, Annesi-Maesano I, Bateman ED, Ben Kheder A, Boakye DA, Bouchard J, Burney P, Busse WW, Chan-Yeung M, Chavannes NH, Chuchalin A, Dolen WK, Emuzyte R, Grouse L, Humbert M, Jackson C, Johnston SL, Keith PK, Kemp JP, Klossek JM, Larenas-Linnemann D, Lipworth B, Malo JL, Marshall GD, Naspitz C, Nekam K, Niggemann B, Nizankowska-Mogilnicka E, Okamoto Y, Orru MP, Potter P, Price D, Stoloff SW, Vandenplas O, Viegi G, Williams D: Allergic Rhinitis and its Impact on Asthma (ARIA) 2008 update (in collaboration with the World Health Organization, GA(2)LEN and AllerGen). Allergy 2008; 63(Suppl 86):8–160

16. Szczeklik A, Stevenson DD: Aspirin-induced asthma: Advances in pathogenesis, diagnosis, and management. J Allergy Clin Immunol 2003; 111:913–21

17. Kumeta Y, Hattori A, Mimura M, Kishikawa K, Namiki A: A survey of perioperative bronchospasm in 105 patients with reactive airway disease. Masui 1995; 44:396–401

18. Schwilk B, Bothner U, Schraag S, Georgieff M: Perioperative respiratory events in smokers and nonsmokers undergoing general anaesthesia. Acta Anaesthesiol Scand 1997; 41:348–55

19. Westhorpe RN, Ludbrook GL, Helps SC: Crisis management during anaesthesia: Bronchospasm. Qual Saf Health Care 2005; 14:e7

20. Cheney FW, Posner KL, Lee LA, Caplan RA, Domino KB: Trends in anesthesia-related death and brain damage: A closed claims analysis. Anesthesiology 2006; 105:1081–6

21. Cook TM, Bland L, Mihai R, Scott S: Litigation related to anaesthesia: An analysis of claims against the NHS in England 1995–2007. Anaesthesia 2009; 64:706–18

22. Auroy Y, Benhamou D, Péquignot F, Bovet M, Jougla E, Lienhart A: Mortality related to anaesthesia in France: Analysis of deaths related to airway complications. Anaesthesia 2009; 64:366–70

23. Haxhiu MA, Kc P, Moore CT, Acquah SS, Wilson CG, Zaidi SI, Massari VJ, Ferguson DG: Brain stem excitatory and inhibitory signaling pathways regulating bronchoconstrictive responses. J Appl Physiol 2005; 98:1961–82

24. Jooste EH, Sharma A, Zhang Y, Emala CW: Rapacuronium augments acetylcholine-induced bronchoconstriction via positive allosteric interactions at the M3 muscarinic receptor. Anesthesiology 2005; 103:1195–203

25. Kil HK, Rooke GA, Ryan-Dykes MA, Bishop MJ: Effect of prophylactic bronchodilator treatment on lung resistance after tracheal intubation. Anesthesiology 1994; 81:43–8

26. Joos GF: The role of sensory neuropeptides in the pathogenesis of bronchial asthma. Clin Exp Allergy 1989; 19(Suppl 1):9–13

27. Gleason NR, Gallos G, Zhang Y, Emala CW: Propofol preferentially relaxes neurokinin receptor-2-induced airway smooth muscle contraction in guinea pig trachea. Anesthesiology 2010; 112:1335–44

28. Pizov R, Brown RH, Weiss YS, Baranov D, Hennes H, Baker S, Hirshman CA: Wheezing during induction of general anesthesia in patients with and without asthma. A randomized blinded trial Anesthesiology 1995; 82:1111–6

29. Brown RH: HRCT imaging of airway responsiveness: Effects of anesthetics. J Clin Monit Comput 2000; 16:443–55

30. Belelli D, Pistis M, Peters JA, Lambert JJ: General anaesthetic action at transmitter-gated inhibitory amino acid receptors. Trends Pharmacol Sci 1999; 20:496–502

31. Hirshman CA, Edelstein G, Peetz S, Wayne R, Downes H: Mechanism of action of inhalational anesthesia on airways. Anesthesiology 1982; 56:107–11

32. Gallos G, Gleason NR, Virag L, Zhang Y, Mizuta K, Whittington RA, Emala CW: Endogenous gamma-aminobutyric acid modulates tonic guinea pig airway tone and propofol-induced airway smooth muscle relaxation. Anesthesiology 2009; 110:748–58

33. Akao M, Hirasaki A, Jones KA, Wong GY, Bremerich DH, Warner DO: Halothane reduces myofilament Ca2+ sensitivity during muscarinic receptor stimulation of airway smooth muscle. Am J Physiol 1996; 271:L719–25

34. Schaub B, von Mutius E: Obesity and asthma, what are the links? Curr Opin Allergy Clin Immunol 2005; 5:185–93

35. Weiss ST, Shore S: Obesity and asthma: Directions for research. Am J Respir Crit Care Med 2004; 169:963–8

36. Liccardi G, Salzillo A, De Blasio F, D'Amato G: Control of asthma for reducing the risk of bronchospasm in asthmatics undergoing general anesthesia and/or intravascular administration of radiographic contrast media. Curr Med Res Opin 2009; 25:1621–30

37. Smetana GW: Preoperative pulmonary evaluation. N Engl J Med 1999; 340:937–44

38. Sweitzer BJ, Smetana GW: Identification and evaluation of the patient with lung disease. Anesthesiol Clin 2009; 27:673–86

39. Ortega VE, Peters SP: Beta-2 adrenergic agonists: Focus on safety and benefits versus risks. Curr Opin Pharmacol 2010; 10:246–53

40. Kramer JM: Balancing the benefits and risks of inhaled long-acting agonists: The influence of values. N Engl J Med 2009; 360:1592–5

41. Barnes PJ: Mechanisms of action of glucocorticoids in asthma. Am J Respir Crit Care Med 1996; 154:S21–6; discussion S26–7

42. Peters SP, Kunselman SJ, Icitovic N, Moore WC, Pascual R, Ameredes BT, Boushey HA, Calhoun WJ, Castro M, Cherniack RM, Craig T, Denlinger L, Engle LL, DiMango EA, Fahy JV, Israel E, Jarjour N, Kazani SD, Kraft M, Lazarus SC, Lemanske RF Jr, Lugogo N, Martin RJ, Meyers DA, Ramsdell J, Sorkness CA, Sutherland ER, Szefler SJ, Wasserman SI, Walter MJ, Wechsler ME, Chinchilli VM, Bleecker ER: National Heart, Lung, and Blood Institute Asthma Clinical Research Network: Tiotropium bromide step-up therapy for adults with uncontrolled asthma. N Engl J Med 2010; 363:1715–26

43. Goff MJ, Arain SR, Ficke DJ, Uhrich TD, Ebert TJ: Absence of bronchodilation during desflurane anesthesia: A comparison to sevoflurane and thiopental. Anesthesiology 2000; 93:404–8

44. Osuorji I, Williams C, Hessney J, Patel T, Hsi D: Acute stress cardiomyopathy following treatment of status asthmaticus. South Med J 2009; 102:301–3

45. Green SM: Intravenous epinephrine in asthma? A word of caution. Ann Emerg Med 2003; 41:712–3

46. Holley DA, Boots RJ: Management of acute severe and near-fatal asthma. Emerg Med Australas 2009; 21:259–68

∥ Grade I: Erythema, urticaria with or without angioedema; grade II: cutaneous-mucous signs ± hypotension ± tachycardia ± dyspnea ± gastrointestinal disturbances; grade III: cardiovascular collapse, tachycardia, or bradycardia ± cardiac dysrythmia ± bronchospasm ± cutaneous-mucous signs ± gastrointestinal disturbances; grade IV: cardiac arrest. Cited Here...
# Association Française de Chirurgie & Société Française d'Anesthésie et de Réanimation & Office Français de Prévention du Tabagisme: Conférence d'Experts. Tabagisme péri-opératoire, 2005. Available at: http://www.sfar.org/_docs/articles/151-Tabagisme%20p%C3%A9riop%C3%A9ratoire-recommandations.pdf. Accessed January 12, 2011. Cited Here...
** British Thoracic Society & Scottish, Intercollegiate Guidelines Network: British Guideline on the Management of Asthma: A National Clinical Guideline. May 2008. Revised June 2009. Available at: http://www.sign.ac.uk/pdf/sign101.pdf. Accessed January 12, 2011. Cited Here...

© 2011 American Society of Anesthesiologists, Inc.

Publication of an advertisement in Anesthesiology Online does not constitute endorsement by the American Society of Anesthesiologists, Inc. or Lippincott Williams & Wilkins, Inc. of the product or service being advertised.
Login

Article Tools

Images

CME Test

Share