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Title: Dr abdollahi


1
Anesthesia and pulmonary diseases
  • Dr abdollahi

2
  • Thoracic and upper abdominal operations are a
    particular risk for patients with chronic
    pulmonary disease.

3
Obstructive airway diseases
  • Asthma and chronic obstructive pulmonary disease
    (COPD), the two major categories of obstructive
    airway disease, affect millions of Americans and
    cause significant morbidity and mortality
    worldwide.

4
  • Asthma is a chronic inflammatory disorder of the
    airways characterized by variable airflow
    obstruction, airway inflammation, and bronchial
    hyperresponsiveness.

5
  • In contrast, the airflow obstruction in COPD is
    defined as progressive and not fully reversible.
    The chronic inflammation of the airways and lung
    parenchyma in COPD is most often secondary to
    cigarette smoke exposure.

6
  • Together, asthma and COPD constitute a major
    public health concern, and a basic understanding
    of these diseases is important when caring for
    patients who receive anesthesia.

7
ASTHMA
  • Asthma is a disease that is defined by the
    presence of
  • (1) Chronic inflammatory changes in the
    submucosa of the airways
  • (2) Airway hyperresponsiveness
  • (3) Reversible expiratory airflow obstruction.

8
  • Airway hyperresponsiveness characterizes this
    disease, even in asymptomatic patients, and is
    demonstrated by the development of
    bronchoconstriction in response to stimuli
    (allergens, exercise, mechanical airway
    stimulation) that have little or no effect on
    normal airways. Airway hyper responsiveness
    elicited during methacholine bronchoprovocation
    and airway bronchodilation in response to inhaled
    albuterol help diagnose asthma.

9
Clinical Symptoms
  • The classic symptoms associated with asthma are
    cough, shortness of breath, and wheezing.
    However, symptoms of asthma may vary and range
    from cough with or without sputum production to
    chest pain or tightness. Chronic,
  • nonproductive cough may be the sole initial
    complaint.

10
  • Some asthmatics also experience symptoms
    exclusively
  • with exertion ("exercise-induced asthma"), and
    this diagnosis
  • is a consideration in the pediatric and young
    adult population.

11
  • The presence or absence of wheezing on physical
    examination is a poor predictor of the severity
    of airflow obstruction. Thus, the presence of
    wheezing suggests airway narrowing, which should
    be confirmed and quantified by spirometry.

12
  • Degrees of obstraction are defined according to
    the FEV1 predicted .
  • Reversibility of obstruction after the
    administration of a
  • bronchodilator suggests a diagnosis of asthma.

13
  • An increase in FEV1 predicted of more than 12
    and an increase in FEVl of greater than 0.2 L
    suggest acute bronchodilator responsiveness and
    variability in airflow obstruction.
  • In contrast, the airways of patients with COPD do
    not demonstrate reversibility of airflow
    obstruction to the same degree as do those with
    asthma, a characteristic that can help
    distinguish these two causes of airflow
    obstraction.

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  • During severe asthma exacerbations, intravenous
    therapy
  • with glucocorticoids is the mainstay of therapy.
    In rare
  • circumstances, when life-threatening status
    asthmaticus
  • persists despite aggressive pharmacologic
    therapy, it may
  • be necessary to consider general anesthesia
    (isoflurane or
  • sevoflurane) in an attempt to produce
    bronchodilation.

17
Management of Anesthesia
  • Pulmonary function studies (especially FEV1)
    obtained
  • before and after bronchodilator therapy may be
    indicated
  • in a patient with asthma who is scheduled for a
    thoracic
  • or abdominal operation. Measurement of arterial
    blood
  • gases before proceeding with elective surgery is
    a consideration
  • if there are questions about the adequacy of
    ventilation or arterial oxygenation.

18
  • All asthmatics who have persistent symptoms
    should be treated with either inhaled or systemic
    corticosteroids (depending on the severity of
    their airflow obstruction), in addition to
    scheduled dose of inhaled beta agonists. Therapy
    should be continued throughout the perioperative
    period. Supplementation with cortisol may be
    indicated before major surgery for
    corticosteroid-dependent asthmatics because of
    suppression of the hypothalamic-pituitary-adrenal
    axis.

19
REGIONAL ANESTHESIA
  • Regional anesthesia may be preferred when the
    surgery is
  • superficial or involves the extremities. Notably,
    however,
  • bronchospasm has been reported in asthmatics who
    have received spinal anesthesia, although it is
    generally accepted that regional anesthesia is
    associated with lower complication rates related
    to bronchospasm in the asthmatic population.

20
GENERAL ANESTHESIA
  • The goal during induction and maintenance of
    general anesthesia in patients with asthma is to
    depress airway reflexes in order to avoid
    bronchoconstriction in response to mechanical
    stimulation of the airway. Before tracheal
    intubation, a sufficient depth of anesthesia
    should be
  • established to minimize bronchoconstriction with
    subsequent
  • stimulation of the airway. Rapid intravenous
    induction of anesthesia is most often
    accomplished with the administration of propofol
    or thiopental. Propofol
  • may blunt tracheal intubation-induced
    bronchospasm in
  • patients with asthma.

21
  • ketamine (1 to 2 mg/kg IV) is an alternative
    selection for rapid induction of anesthesia
    because its sympathomimetic effects on bronchial
    smooth muscle may decrease airway resistance. The
    increased secretions associated with the
    administration of ketamine, however, may limit
    the use of this drug in patients with asthma.
  • Sevoflurane and isoflurane are potent volatile
    anesthetics that depress airway reflexes and do
    not sensitize the heart to the cardiac effects of
    the sympathetic nervous system stimulation
    produced by beta-agonists and aminophylline.

22
  • Bronchodilation with sevoflurane and isoflurane
    depends on the ability of the normal airway
    epithelium to produce nitric oxide and
    prostanoids. Halothane is also an effective
    bronchodilator but may be associated with cardiac
    dysrhythmias in the presence of sympathetic
    nervous system stimulation.
  • Desflurane may be accompanied by increased
    secretions,
  • coughing, laryngospasm, and bronchospasm as a
    result of
  • in vivo airway irritation.

23
  • Although case reports suggest that
    bronchodilation follows the intravenous
    administration of lidocaine, the clinical
    significance of this response is unclear and the
    data are equivocal.

24
  • In asthmatic patients undergoing tracheal
    intubation, premedication with inhaled albuterol
    should be the first choice of therapy to prevent
    intubation-induced bronchoconstriction.
  • Neuromuscular blocking drugs that are not
    associated with endogenous histamine release may
    also be used in patients with asthma .

25
  • Although histamine release has been attributed to
    succinylcholine,there is no evidence that this
    drug is associated with increased airway
    resistance in patients with asthma.

26
  • Intraoperatively, Pao2 and Paco2 can be
    maintained at
  • normal levels by mechanical ventilation of the
    lungs at
  • a slow breathing rate (6 to 10 breaths/min) to
    allow
  • adequate time for exhalation, an important
    maneuver
  • in patients with increased airway resistance.
    This slow
  • breathing rate can usually be facilitated by the
    use of a
  • high inspiratory flow rate to allow the longest
    possible
  • time for exhalation. Positive end-expiratory
    pressure
  • (PEEP) should be used cautiously because of the
    inherent,
  • impaired exhalation in the presence of narrowed
    airways.

27
  • At the conclusion of elective surgery, the
    trachea may be extubated while the depth of
    anesthesia is still sufficient to suppress airway
    reflexes. After the administration of
    anticholinesterase drugs to reverse the effects
    of nondepolarizing neuromuscular blocking drugs,
    bronchospasm may occur but is not usual, which
    may reflect the protective effects (decreased
    airway resistance) of simultaneously administered
    anticholinergics. When extubation is delayed for
    reasons of safety until the patient is awake
    (possible presence of gastric contents),
    intravenous administration of lidocaine may
    decrease the likelihood of airway stimulation as
    a result of the endotracheal tube in an awake
    patient.

28
Intraoperative Bronchospasm
  • Airway instmmentation can cause severe reflex
    bronchoconstriction and bronchospasm, especially
    in asthmatic patients with hyperactive airways.
    The bronchospasm that occurs intraoperatively is
    usually due to factors other than acute
    exacerbation of asthma. The frequency of
    perioperative bronchospasm in patients with
    asthma is low, especially if their asthma is
    asymptomatic at the time of surgery.

29
  • It is important to first consider mechanical
    causes of obstruction and inadequate levels of
    anesthesia before initiating treatment of
    intraoperative bronchospasm.
  • Fiberoptic bronchoscopy may be useful to rule out
    mechanical obstraction in the tracheal tube.
    Asthma related
  • bronchospasm may respond to deepening of
    anesthesia with a volatile anesthetic.

30
  • If the bronchospasm is due to asthma and persists
    despite an increase in the concentration of
    delivered anesthetic drug, albuterol should be
    administered by attaching a metered-dose inhaler
    to the anesthetic delivery system. When
    bronchospasm persists despite B2- agonist
    therapy, it may be necessary to add intravenous
    corticosteroids.

31
CHRONIC OBSTRUCTIVE PULMONARY DISEASE
EMPHYSEMA AND CHRONIC BRONCHITIS
  • COPD consists of two entities, emphysema and
    chronic
  • bronchitis. The Global Initiative for Chronic
    Obstructive
  • Lung Disease (GOLD) guidelines provide criteria
  • for diagnosis and classification of severity in
    patients with
  • symptoms of chronic cough, sputum production, or
    exposure
  • to cigarette smoke .

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  • Emphysema is characterized by loss of elastic
    recoil of the lungs, which results in collapse of
    the airways during exhalation and increased
    airway resistance.

34
  • Chronic bronchitis is defined by the presence of
    cough and sputum production for 3 months in each
    of 2 successive years in a patient with risk
    factors, most commonly cigarette smoking. It has
    been estimated that 25 of surgical patients
    smoke and a further 25 are ex-smokers, thus
    making COPD an important diagnosis to consider in
    any patient undergoing anesthesia.

35
Prediction of Postoperative Outcome
  • The need for preoperative pulmonary function
    studies
  • in patients with COPD is controversial because of
    the
  • questionable correlation of these tests with
    postoperative
  • outcome. Although the FEV! predicted has been
    used
  • to grade the severity of airflow obstraction,
    data have
  • shown that using a multidimensional grading
    system to
  • assess the respiratory and systemic extent of
    COPD is a
  • better predictor of mortality than using FEV,
    alone.

36
BODE index.
  • This grading system is based on four variables-
  • 1Body mass index (B)
  • 2Severity of airflow obstraction (0)
  • 3Functional dyspnea (D)
  • 4Exercise capacity as assessed by the 6-minute
    walk test (E)

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  • Patients with higher BODE scores were at higher
    risk for death. Hypercapnia and hypoxemia, as
    detected by arterial blood gas analysis, may also
    characterize patients with moderate to severe
    airflow obstmction. Chronic hypoxemia may lead to
  • pulmonary hypertension and cor pulmonale.
    Preoperative
  • detection plus treatment of hypoxemia-induced cor
  • pulmonale with supplemental oxygen is an
    important
  • part of preoperative management.

39
Management of Anesthesia
  • The presence of COPD does not dictate the use of
    specific
  • management of anesthesia. If general anesthesia
    is selected, a volatile anesthetic with
    humidified inhaled gases and mechanical
    ventilation of the lungs is useful. drugs or
    techniques (regional or general) for the
    management of anesthesia.

40
  • Nitrous oxide may be used, but potential
    disadvantages include
  • limitation of the inhaled concentrations of
    oxygen and passage of nitrous oxide into
    emphysematous bullae.
  • Nitrous oxide could lead to enlargement and
    rupture of these bullae and result in the
    development of tension pneumothorax.

41
  • Opioids are acceptable but are less ideal for
    maintenance of anesthesia because of the frequent
    need for high inhaled concentrations of nitrous
    oxide to ensure amnesia and associated decreases
    in inhaled concentrations of oxygen. To avoid
    this problem, administration of a volatile
    anesthetic at a low concentration may be
    substituted for nitrous oxide. Postoperative
    depression of ventilation may also reflect the
    residual effects of opioids administered
    intraoperatively.

42
MANAGEMENTOF VENTILATION
  • Patients with COPD are ventilated in a manner
    similar to
  • those with asthma. Small tidal volumes may be
    delivered
  • to decrease the likelihood of gas trapping and
    barotrauma.
  • Slow breathing rates are used to permit maximal
    time for
  • exhalation. Continued tracheal intubation and
    mechanical
  • ventilation of the lungs in the postoperative
    period are
  • often necessary after major surgery in patients
    with severe
  • emphysema. Postoperative depression of
    ventilation may
  • also reflect the residual effects of opioids
    administered.

43
  • Hypercapnia secondary to chronic hypoventilation
    should not be corrected intraoperatively because
    it may then be difficult to wean the patient from
    mechanical ventilation as a result of the
    decreased respiratory drive in patients who
    chronically hypoventilate.

44
Pulmonary HYPERTENSION
  • Pulmonary hypertension is defined as an elevation
    in
  • mean pulmonary artery pressure to levels higher
    than
  • 25 mm Hg at rest or higher than 30 mm Hg with
    exercise.
  • Most cases of pulmonary hypertension are
    secondary to
  • cardiac or pulmonary disease in a minority of
    cases, the
  • etiology is unknown and the pulmonary
    hypertension is
  • considered primary.

45
Classification
  • The World Health Organization has proposed a
    classification
  • of pulmonary hypertension that includes pulmonary
  • hypertension secondary to left heart disease,
    pulmonary
  • disease, vascular disease, and primary pulmonary
    hypertension.
  • Indicators of disease severity include dyspnea
    at rest, hypoxemia, syncope, metabolic acidosis
    indicating
  • low cardiac output, and signs of right heart
    failure on
  • physical examination (elevated jugular venous
    pressure,
  • hepatomegaly, and peripheral edema).

46
Diagnostic Evaluation
  • Diagnostic evaluation for pulmonary hypertension
    includes
  • the electrocardiogram echocardiogram chest
    roentgenogram
  • assessment for secondary causes such as pulmonary
  • embolism (computed tomographic angiography or
  • ventilation/perfusion scanning), underlying
    pulmonary
  • disease (pulmonary function testing), collagen
    vascular
  • disease, or liver failure and right heart
    catheterization.

47
  • Right heart catheterization is the gold standard
    for diagnosis
  • because it provides data on the severity of
    pulmonary
  • artery hypertension, as well as pulmonary venous
    pressure
  • and cardiac output, which have prognostic
    significance.
  • In addition, right heart catheterization is a
    necessary part
  • of testing for vasodilator response, the first
    step in the
  • algorithm to determine appropriate therapy for
    pulmonary
  • artery hypertension.

48
Pathophysiology
  • Chronic elevation of pulmonary artery pressure
    leads to
  • elevated right ventricular systolic pressure,
    hypertrophy
  • and dilatation of the right ventricle, and
    resultant right
  • ventricular failure. Right ventricular preload
    and pulmonary
  • blood flow are dependent on venous return in this
    setting.

49
Management of Anesthesia
  • Intraoperative considerations for a patient with
    severe pulmonary hypertension include maintaining
    adequate preload, minimizing tachycardia and
    cardiac dysrhythmias that may decrease cardiac
    output, and avoiding arterial hypoxemia and
    hypercapnia, which can increase pulmonary
    vascular resistance (PVR). Cardiac output from a
    failing right ventricle is critically dependent
    on filling pressure from venous return and
    pulmonary pressure.

50
  • Options for treatment of pulmonary hypertension
    during surgery include inhaled nitric oxide (10
    ppm), inhaled prostacyclin (either intermittent
    or continuous), and phosphodiesterase inhibitors
    such as milrinone. Pulmonary artery catheters
    have been used for intraoperative monitoring.

51
PARTURIENTS
  • Mortality in pregnant patients undergoing vaginal
    delivery
  • is near 50 and may be even higher when cesarean
    delivery
  • is performed. Most often, vaginal deliveries are
    preferred,
  • although regional anesthesia may be used
    successfully during
  • cesarean sections. The danger of decreased venous
    return
  • secondary to the sympathetic nervous system
    blockade
  • produced by regional anesthesia should be
    considered.

52
POSTOPERATIVE PERIOD
  • In the postoperative period, care must be taken
    to avoid
  • large-volume fluid shifts, arterial hypoxemia,
    systemic
  • hypotension, and hypovolemia in patients with
    pulmonary
  • hypertension. Morbidity and mortality in the
    postoperative
  • period are significant concerns, with possible
    causes
  • including pulmonary vasospasm, increases in
    pulmonary
  • artery pressure, fluid shifts, cardiac
    dysrhythmias, and
  • heightened sympathetic nervous system tone.

53
OBSTRUCTIVE SLEEP APNEA
  • Patients with obstructive sleep apnea (OSA) are
    at high risk for postoperative complications when
    undergoing general anesthesia. OSA is reported to
    occur in 2 of middle-aged women and 4 of
    middle-aged men. It is suspected, however, that
    up to 80 of cases of OSA are undiagnosed, thus
    suggesting that those with this disorder may be a
    significant portion of the surgical population.

54
  • Obesity is the most significant risk factor for
    the development
  • of OSA, with a body mass index greater than 30
    and a large neck circumference (gt44 cm) being
    positively correlated with severe OSA. Obese
    patients with OSA or suspected OSA are at risk
    for complications during tracheal intubation and
    extubation, as well as during the postoperative
    period.,

55
  • Comorbid medical illnesses such as hypertension
    cardiovascular disease, and congestive heart
    failure are also more prevalent in patients with
    OSA than in the general population, a fact that
    contributes to their postoperative morbidity.
    Systemic hypertension has been reported in up to
    50 of patients with OSA and is independent of
    obesity, age, and gender.

56
  • Treatment of OSA by noninvasive ventilation
    results in better control of systemic
    hypertension. In addition to systemic
    hypertension, pulmonary hypertension is more
    prevalent in these patients than in the general
    population, One common
  • mechanism that may explain both the systemic and
    pulmonary
  • hypertension in patients with OSA is the chronic
    decrease
  • in Pa02 during apneic episodes.

57
Management of Anesthesia
  • Evaluation of the oral cavity in patients with
    OSA may not reveal the true nature of their
    pharyngeal space because increased fat deposition
    in the lateral pharyngeal walls has been
    demonstrated in these patients and shown to
    correlate with the severity of OSA. Neck
    circumference reflects pharyngeal fat deposition
    and correlates more strongly with the incidence
    and severity of OSA than general obesity dose.

58
IMPACT OF SEDATIVE DRUGS
  • Relaxation of the upper airway musculature in
    response to benzodiazepines may significantly
    reduce the pharyngeal
  • space and result in longer periods of hypopnea,
    arterial hypoxemia, and hypercapnia in patients
    with OSA than in the general population.

59
  • Any medications that depress the central nervous
    system must be administered carefully because
    airway patency and skeletal muscle tone,
    maintained in the awake state, may be lost at the
  • onset of sleep. In addition, opioid analgesics
    may decrease
  • the central respiratory drive and thus further
    add to the
  • possible complications of sedation.

60
ANTICIPATION OF DIFFICULT AIRWAY MANAGEMENT
  • Full preparation for difficult airway management,
    including
  • the availability of orotracheal tubes of various
    size, a
  • Fastrach laryngeal mask, and a fiberoptic
    bronchoscope,
  • should be made before initiating direct
    laryngoscopy for
  • tracheal intubation.

61
  • Adequate preoxygenation is necessary in obese
    patients with OSA because of their reduced
    functional residual capacity and risk for
    arterial hypoxemia with induction of anesthesia.
    Tracheal extubation should be performed only when
    the patient is breathing spontaneously with
    adequate tidal volumes, oxygenation, and
    ventilation.

62
MANAGEMENTIN THE POSTOPERATIVE PERIOD
  • Respiratory depression and repetitive apnea in
    the postoperative period can occur in patients
    with OSA,
  • especially in the setting of opioid
    administration for pain
  • control. It should also be noted that in patients
    with OSAwho hypoventilate (obesity-hypoventilation
    syndrome),
  • careful documentation of preoperative arterial
    blood gases is necessary to establish the
    baselinc set point for ventilation, an important
    factor whcn considering the patient's respiratory
    drive after extubation.

63
  • Relativc hyperventilation intraoperatively to
    maintain a norma Paco2 in subjects who
    chronically hypoventilate may result in prolonged
    apnea when attempting extubation.

64
Smoking Cessation
  • The risk for postoperative pulmonary
    complications among smokers as opposed to
    nonsmokers is greatly increased.The length of
    preoperative smoking cessation necessary to
    decrease this risk is not clear. It is generally
    accepted that the increased incidence of
    postoperative pulmonary complications in smokers
    can be reduced significantly by persuading the
    patient to stop smoking before surgery, although
    there is no consensus on the minimal or optimal
    duration of preoperative abstinence.

65
DISCONTINUATION OF SMOKING
  • Smoking increases airway irritability and
    secretions, decreases mucociliary transport, and
    increases the incidence of postoperative
    pulmonary complications. Cessation of smoking for
    12 to 24 hours before surgery decreases the level
    of carboxyhemoglobin, shifts the oxyhemoglobin
  • dissociation curve to the right, and increases
    the oxygen available to tissues.

66
  • In contrast to these short-term effects,
    improvement in mucociliary transport and small
    airway function and decreases in sputum
    production require prolonged abstinence (8 to 12
    weeks) from smoking. The incidence of
    postoperative pulmonary complications decreases
    with abstinence from cigarette smoking for

67
  • Nevertheless, it is useful to encourage smoking
    abstinence in the perioperative
  • period, especially because smoking shortly before
    surgery may be associated with an increased
    incidence of ST-segment depression on the
    electrocardiogram.

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Tuberculosis
70
Tuberculosis
  • Mycobacterium tuberculosis is an obligate aerobe
    responsible for TB. This organism survives most
    successfully in tissues with high oxygen
    concentrations, which is consistent with the
    increased presentation of TB in the apices of the
    lungs.

71
  • Almost all M. tuberculosis infections result from
    aerosol (droplet) inhalation. It has been
    estimated that up to 600,000 droplet nuclei are
    expelled with each cough and remain viable for
    several days. Although a single infectious unit
    is capable of causing infection in susceptible
    individuals, prolonged exposure in closed
    environments is optimal for transmission of
    infection.

72
  • It is estimated that 90 of patients infected
    with M. tuberculosis never become symptomatic and
    are identified only by conversion of the
    tuberculin skin test. Often patients who acquire
    the infection early in life do not become
    symptomatic until much later. Patients who are
    HIV seropositive or immunocompromised are at much
    higher risk of becoming symptomatic

73
  • Sputum smears and cultures are also used to
    diagnose TB. Smears are examined for the presence
    of acid-fast bacilli. This test is based on the
    ability of mycobacteria to take up and retain
    neutral red stains after an acid wash. It is
    estimated that 50 to 80 of individuals with
    active TB have positive sputum smears. Although
    the absence of acid-fast bacilli does not rule
    out TB, a positive sputum culture containing M.
    tuberculosis provides a definitive diagnosis.

74
  • Health care workers are at increased risk of
    occupational acquisition of TB. For example, TB
    is twice as prevalent in physicians as in the
    general population. Persons involved with
    autopsies are uniquely at risk.

75
Diagnosis
  • The diagnosis of TB is based on the presence of
    clinical symptoms, the epidemiologic likelihood
    of infection, and the results of diagnostic
    tests. Symptoms of pulmonary TB often include
    persistent nonproductive cough, anorexia, weight
    loss, chest pain, hemoptysis, and night sweats.
    The most common test for TB is the tuberculin
    skin (Mantoux) test. The skin reaction is read in
    48 to 72 hours, and a positive reading is
    generally defined as an induration of more than
    10 mm.

76
  • For patients with AIDS, a reaction of 5 mm or
    more is considered positive. The skin test is
    limited, and alternative screening and diagnostic
    tests are undergoing evaluation. The skin test is
    nonspecific and may be positive if people have
    received a bacille Calmette-Guérin vaccine or if
    they have been exposed to TB, or perhaps even
    other mycobacteria, even if there are no viable
    mycobacteria present at the time of the skin test.

77
  • Chest radiographs are important for the diagnosis
    of TB. Apical or subapical infiltrates are highly
    suggestive of infection. Bilateral upper lobe
    infiltration with the presence of cavitation is
    also common. Patients with AIDS may demonstrate a
    less classic picture on chest radiography, which
    may be further confounded by the presence of PCP.
    Tuberculous vertebral osteomyelitis (Pott's
    disease) is a common manifestation of
    extrapulmonary TB.

78
  • Anesthesiologists are at increased risk of
    nosocomial TB by virtue of events surrounding the
    induction and maintenance of anesthesia that may
    induce coughing (tracheal intubation, tracheal
    suctioning, mechanical ventilation).Bronchoscopy
    is a high-risk procedure associated with
    conversion of the tuberculin skin test in
    anesthesiologists. As a first step in preventing
    occupational acquisition of TB, anesthesia
    personnel should participate in annual tuberculin
    screening such that those who develop a positive
    skin test may be offered chemotherapy. The
    decision to take chemotherapy is not trivial as
    treatment for TB carries the serious toxicity. A
    baseline chest radiograph is indicated when a
    positive tuberculin skin test first manifests

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81
Treatment
  • Anti-TB chemotherapy has decreased mortality from
    TB by more than 90.With adequate treatment, more
    than 90 of patients who have susceptible strains
    of TB have bacteriologically negative sputum
    smears within 3 months. In the United States,
    vaccination with bacille Calmette-Guérin is not
    recommended, as it may not confer immunity and
    confounds the diagnosis of TB.

82
  • Some argue that, for protection of the community,
    people who have positive skin tests should
    receive chemotherapy with isoniazid. However, the
    flipside is that isoniazid is a toxic drug and
    treatment is only strictly indicated if there are
    radiographic features of pulmonary TB or if there
    are suggestive symptoms. The toxicity of
    isoniazid manifests in the peripheral nervous
    system, liver, and possibly the kidneys.
    Neurotoxicity may be prevented by daily
    administration of pyridoxine. Hepatotoxicity is
    most likely to be related to metabolism of
    isoniazid by hepatic acetylation. Depending on
    the genetically determined traits, patients may
    be characterized as slow or rapid acetylators.
    Hepatitis appears to be more common in rapid
    acetylators, consistent with the greater
    production of hydrazine, a potentially
    hepatotoxic metabolite of isoniazid. Persistent
    elevations of serum transaminase concentrations
    mandate that isoniazid be discontinued, but mild,
    transient increases do not.

83
  • Other drugs used to treat TB include
    pyrazinamide, rifampicin, and ethambutol. Adverse
    effects of rifampicin include thrombocytopenia,
    leukopenia, anemia, and renal failure. Hepatitis
    associated with increases in serum
    aminotransaminase concentrations occur in
    approximately 10 of patients being treated with
    rifampicin. In order to be curative, treatment
    for pulmonary TB is recommended for 6 months.
    Extrapulmonary TB usually requires a longer
    course. Noncompliance with therapy contributes to
    the emergence of resistant TB strains.

84
Management of Anesthesia
  • The preoperative assessment of patients
    considered to be at risk of TB includes a
    detailed history, including the presence of a
    persistent cough and the tuberculin
    status.Elective surgical procedures should be
    postponed until patients are no longer considered
    infectious. Patients are considered noninfectious
    if they have received antituberculous
    chemotherapy, are improving clinically, and have
    had three consecutive negative sputum smears.

85
  • If surgery cannot be delayed, it is important to
    limit the number of involved personnel, and high
    risk procedures (bronchoscopy, tracheal
    intubation, and suctioning) should be performed
    in a negative-pressure environment whenever
    possible. Patients should be transported to the
    operating room wearing a tight-fitting N-95 face
    mask to prevent casual exposure of others to
    airborne bacilli. Staff should also wear N-95
    masks.

86
  • If patients have TB of the cervical spine,
    special precautions should be taken not to injure
    the spine during airway manipulation. A high
    efficiency particulate air filter should be
    placed in the anesthesia delivery circuit between
    the Y connector and the mask, laryngeal mask
    airway, or tracheal tube. Bacterial filters
    should be placed on the exhalation limb of the
    anesthesia delivery circuit to decrease the
    discharge of tubercle bacilli into the ambient
    air. Sterilization of anesthesia equipment
    (laryngoscope blades) is with standard methods
    using a disinfectant that destroys tubercle
    bacilli.

87
  • Use of a dedicated anesthesia machine and
    ventilator is recommended. Positive-pressure
    ventilation has been associated with massive
    hemoptysis in a patient with old pulmonary TB
    leading to the recommendation that maintenance of
    spontaneous breathing may be indicated in
    selected patients. Postoperative care should, if
    possible, take place in an isolation room,
    preferably with negative pressure.

88
lists important considerations in regard to
tuberculosis.
  1. With the acquired immunodeficiency syndrome
    epidemic, tuberculosis is reemerging worldwide.
  2.    Multidrug resistant and extensively
    drug-resistant strains are resistant to therapy
    and have increased virulence.   
  3. Symptoms include persistent cough, anorexia,
    weight loss, chest pain, hemoptysis, and night
    sweats.  
  4.   Anesthesiologists are at increased risk of
    nosocomial tuberculosis.   
  5. Treatment for pulmonary tuberculosis is
    recommended for 6 months.   

89
  • 6. Noncompliance with therapy contributes to the
    emergence of resistant tuberculosis strains.   
  • 7. Staff and patients should wear N-95 masks.  
  •  8. A dedicated anesthesia machine and
    ventilator should ideally be used.   
  • 9. Postoperative care should take place in an
    isolation room with negative pressure.

90
UPPER RESPIRATORY TRACT INFECTIONS
  • Patients may arrive at the hospital for elective
    tonsillectomy and adenoidectomy with an acute
    upper respiratory tract infection. Surgery for
    these patients is usually postponed until
    resolution of the upper respiratory tract
    infection, which is typically 7 to 14 days.
    Laryngospasm with airway manipulation may be more
    likely to occur in the presence of an upper
    respiratory tract infection.

91
  • URI has diffuse effects on the respiratory
    epithelium, mucociliary function, and airway
    reactivity. These effects combine to provide the
    potential for an increased risk for anesthesia in
    specific clinical settings. If the planned
    surgical
  • procedure is short and airway support is
    restricted to the use of a facemask, the risk for
    an adverse respiratory event is minimal.

92
  • If an endotracheal tube is required, the risk for
    an adverse respiratory event is increased (up to
    10- fold) over that in an infant without a URI
    whose trachea
  • is not intubated. An LMA seems to be associated
    with risks midway between those associated with a
    facemask and those with an endotracheal tube.
    Younger age plus a ORI seems to be associated
    with an increased risk from anesthesia. URIs
    develop recurrently in 1- to 6-year-olds, and if
    reactive airways accompany the infection, the
    effect on the airway persists for 2 to 6 weeks.

93
  • Ultimately, the preoperative evaluation must
    weigh the inconvenience of rescheduling
  • against ignoring possible risks. If the decision
    is to
  • proceed with elective surgery, the infant should
    be
  • considered to have reactive airways.

94
  • The decision to cancel surgery on a child with an
    uncomplicated ORI always requires assessment from
    the viewpoint of a specific patient and family, a
    specific procedure, and a specific surgeon. A
    strict protocol for when to
  • cancel surgery is impractical. The patient's age,
    medical and anesthetic history, current physical
    examination, planned surgery (placement of
    tympanostomy tubes versus surgery for
    craniofacial repair), and anticipated
    postoperative care (need for mechanical
    ventilatory support) must be analyzed.

95
  • Ultimately, the preoperative evaluation must
    weigh the inconvenience of rescheduling against
    ignoring possible risks. If the decision is to
    proceed with elective surgery, the infant should
    be considered to have reactive airways.

96
Epiglottitis
  • Acute epiglottitis is an infectious disease
    caused by Haernopbilus infiuenzae type B. It can
    progress rapidly from a sore throat, to airway
    obstruction, to respiratory
  • failure and death if proper diagnosis and
    treatment are delayed. Patients are usually
    between 2 and 7 years of age, although
    epiglottitis has been reported in younger
  • children and adults.

97
  • Characteristic signs and symptoms of acute
    epiglottitis include
  • (1) a sudden onset of fever, dysphagia,
    drooling, thick muffled voice, and preference for
    the sitting position with the head extended and
    leaning forward (2) retractions, labored
    breathing, and cyanosis when respiratory
    obstruction is present.

98
Treatment
  • Direct visualization of the epiglottis should not
    be attempted in an awake patient because it could
    lead to airway compromise and death. Interactions
    with the patient should be kept to a minimum.
    Stimulation of the patient or the onset
  • of struggling during attempted treatment
    procedures may result in exacerbation of the
    airway obstruction. Induction of anesthesia is
    often accomplished with the
  • inhalation of sevoflurane (alternatively,
    halothane) while maintaining spontaneous
    ventilation.

99
  • It is important to secure the airway without
    stimulating the reactive airway.
  • An emergency airway cart and tracheostomy tray
    should be available and open, with appropriate
    personnel present should an emergency surgical
    airway be needed.

100
  • Postoperative management takes place in the
    intensive care unit and consists of continued
    observation and radiographic confirmation of
    tracheal tube placement. Tracheal extubation is
    usually attempted 48 to 72 hours
  • later when a significant leak around the
    endotracheal tube is present and visual
    inspection of the larynx by flexible fiberoptic
    bronchoscopy confirms a reduction in swelling of
    the epiglottis and surrounding tissue.

101
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