harrison ˇs principles of internal medicine,17th edition ... 21/ghalb.pdf.390.pdf ·...
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• Harrison’s Principles of Internal Medicine, 17th Edition,Chapter 354
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• A 67-year-old man presents with a history of dyspnea,which has progressed for the past several years.
• He began smoking cigarettes at 15 years of age andcontinues to smoke one pack per day. Worseningbreathlessness forced him to retire as a laborer, and hehas sought emergency care for what he calls bronchitistwice in the past year.
• His physical examination is notable for diminishedbreath sounds on auscultation, with a prolongedexpiratory phase.
• Spirometry reveals severe airflow obstruction (ratio offorced expiratory volume in 1 second [FEV1] to forcedvital capacity [FVC], 0.43; FEV1, 34% of the predictedvalue).
• How should this case be managed?
• A 67-year-old man presents with a history of dyspnea,which has progressed for the past several years.
• He began smoking cigarettes at 15 years of age andcontinues to smoke one pack per day. Worseningbreathlessness forced him to retire as a laborer, and hehas sought emergency care for what he calls bronchitistwice in the past year.
• His physical examination is notable for diminishedbreath sounds on auscultation, with a prolongedexpiratory phase.
• Spirometry reveals severe airflow obstruction (ratio offorced expiratory volume in 1 second [FEV1] to forcedvital capacity [FVC], 0.43; FEV1, 34% of the predictedvalue).
• How should this case be managed?
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A 57-year-old patient who smokes cigarettes presents with chronic productivecough and persistent progressive exercise limitation that is a result ofbreathlessness.
For this patient, which of the following statements is true?
❑ A. Significant airway obstruction occurs in only 10% to 15% of peoplewho smoke
❑ B. The best tool for assessing the severity of obstruction is the ratio offorced expiratory volume in 1 second to forced vital capacity(FEV1/FVC)
❑ C. Chronic bronchitis is a clinical diagnosis defined as the presence ofcough and sputum production on most days for at least 3 consecutivemonths in a year
❑ D. Measurement of lung volumes in patients with chronic airwayobstruction (CAO) uniformly reveals an increased residual volume anda decreased functional residual capacity (FRC)
A 57-year-old patient who smokes cigarettes presents with chronic productivecough and persistent progressive exercise limitation that is a result ofbreathlessness.
For this patient, which of the following statements is true?
❑ A. Significant airway obstruction occurs in only 10% to 15% of peoplewho smoke
❑ B. The best tool for assessing the severity of obstruction is the ratio offorced expiratory volume in 1 second to forced vital capacity(FEV1/FVC)
❑ C. Chronic bronchitis is a clinical diagnosis defined as the presence ofcough and sputum production on most days for at least 3 consecutivemonths in a year
❑ D. Measurement of lung volumes in patients with chronic airwayobstruction (CAO) uniformly reveals an increased residual volume anda decreased functional residual capacity (FRC)
Answer: A
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(Answer: B—
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Answer: D—
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Answer: A—
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Answer: A—
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Answer: C—
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Answer: E—
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Definition• A disease state characterized by airflow
limitation that is not fully reversible• Conditions include:
– Emphysema: anatomically defined conditioncharacterized by destruction and enlargementof the lung alveoli
– Chronic bronchitis: clinically defined conditionwith chronic cough and phlegm
– Small-airways disease: condition in whichsmall bronchioles are narrowed
• A disease state characterized by airflowlimitation that is not fully reversible
• Conditions include:– Emphysema: anatomically defined condition
characterized by destruction and enlargementof the lung alveoli
– Chronic bronchitis: clinically defined conditionwith chronic cough and phlegm
– Small-airways disease: condition in whichsmall bronchioles are narrowed
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Epidemiology
• Fourth leading cause of death in the U.S.• Affects > 16 million persons in the U.S.• Global Initiative for Chronic Obstructive
Lung Disease (GOLD) estimates suggestthat chronic obstructive lung disease(COLD) will increase from the sixth to thethird most common cause of deathworldwide by 2020.
• Fourth leading cause of death in the U.S.• Affects > 16 million persons in the U.S.• Global Initiative for Chronic Obstructive
Lung Disease (GOLD) estimates suggestthat chronic obstructive lung disease(COLD) will increase from the sixth to thethird most common cause of deathworldwide by 2020.
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Epidemiology
• >70% of COLD-related health careexpenditures go to emergency departmentvisits and hospital care (>$10 billionannually in the U.S.).
• >70% of COLD-related health careexpenditures go to emergency departmentvisits and hospital care (>$10 billionannually in the U.S.).
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Epidemiology
Sex• Higher prevalence in men, probably
secondary to smoking• Prevalence of COLD among women is
increasing as the gender gap in smokingrates has diminished.
Sex• Higher prevalence in men, probably
secondary to smoking• Prevalence of COLD among women is
increasing as the gender gap in smokingrates has diminished.
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Age• Higher prevalence with increasing age
– Dose–response relationship betweencigarette smoking intensity and decreasedpulmonary function
Epidemiology
Age• Higher prevalence with increasing age
– Dose–response relationship betweencigarette smoking intensity and decreasedpulmonary function
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Risk FactorsSmoking (see Figure 1)1. Cigarette smoking is a major risk factor.2. Cigar and pipe smoking
Evidence less compelling; likely related tolower dose of inhaled tobacco by-products
3. Passive (secondhand) smokingAssociated with reductions in pulmonary
functionIts status as a risk factor for COLD remains
uncertain
Smoking (see Figure 1)1. Cigarette smoking is a major risk factor.2. Cigar and pipe smoking
Evidence less compelling; likely related tolower dose of inhaled tobacco by-products
3. Passive (secondhand) smokingAssociated with reductions in pulmonary
functionIts status as a risk factor for COLD remains
uncertain
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• Airway hyperresponsiveness• Respiratory infections
– Risk factor for exacerbations– The association of adult and childhood
respiratory infections with development andprogression of COLD remains unproven.
• Airway hyperresponsiveness• Respiratory infections
– Risk factor for exacerbations– The association of adult and childhood
respiratory infections with development andprogression of COLD remains unproven.
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• Occupational exposures to dust and fumes(e.g., cadmium)– Likely risk factors– The magnitude of these effects appears
substantially less important than the effect ofcigarette smoking.
• Ambient air pollution– The relationship of air pollution to COLD
remains unproven.
• Occupational exposures to dust and fumes(e.g., cadmium)– Likely risk factors– The magnitude of these effects appears
substantially less important than the effect ofcigarette smoking.
• Ambient air pollution– The relationship of air pollution to COLD
remains unproven.
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Genetic factors– α1 antitrypsin (α1AT) deficiency– Common M allele: normal levels– S allele: slightly reduced levels– Z allele: markedly reduced levels– Null allele: absence of α1AT (rare)– Lowest levels of α1AT are associated with
incidence of COLD; α1AT deficiencyinteracts with cigarette smoking to increaserisk.
Genetic factors– α1 antitrypsin (α1AT) deficiency– Common M allele: normal levels– S allele: slightly reduced levels– Z allele: markedly reduced levels– Null allele: absence of α1AT (rare)– Lowest levels of α1AT are associated with
incidence of COLD; α1AT deficiencyinteracts with cigarette smoking to increaserisk.
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Distributions of forced expiratory volume in 1 s (FEV1)values in a generalpopulation sample, stratified by pack-years of smoking
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EtiologyCOLD
– Causal relationship between cigarettesmoking and development of COLD has beenproven: however, the response variesconsiderably among individuals.
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COLD exacerbation
– Bacterial infectionsStreptococcus pneumoniaeHaemophilus influenzaeMoraxella catarrhalisMycoplasma pneumoniae or Chlamydia
pneumoniae (5–10% of exacerbations)– Viral infections (one-third)– No specific precipitant identified (20–35%)
– Bacterial infectionsStreptococcus pneumoniaeHaemophilus influenzaeMoraxella catarrhalisMycoplasma pneumoniae or Chlamydia
pneumoniae (5–10% of exacerbations)– Viral infections (one-third)– No specific precipitant identified (20–35%)
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Associated Conditions• Lung cancer• Asthma
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Symptoms & Signs
• 3 most common:– Cough– Sputum production– Exertional dyspnea, frequently of long
duration
• 3 most common:– Cough– Sputum production– Exertional dyspnea, frequently of long
duration
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Additional signs and symptoms• Dyspnea at rest• Prolonged expiratory phase and/or expiratory wheezing
on lung examination• Decreased breath sounds• Barrel chest• Large lung volumes and poor diaphragmatic excursion,
as assessed by percussion• Use of accessory muscles of respiration• Pursed lip breathing (predominantly emphysema)• Characteristic "tripod" sitting position to facilitate the
actions of the sternocleidomastoid, scalene, andintercostal muscles
• Cyanosis, visible in lips and nail beds
• Dyspnea at rest• Prolonged expiratory phase and/or expiratory wheezing
on lung examination• Decreased breath sounds• Barrel chest• Large lung volumes and poor diaphragmatic excursion,
as assessed by percussion• Use of accessory muscles of respiration• Pursed lip breathing (predominantly emphysema)• Characteristic "tripod" sitting position to facilitate the
actions of the sternocleidomastoid, scalene, andintercostal muscles
• Cyanosis, visible in lips and nail beds
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Systemic wastingSignificant weight lossBitemporal wastingDiffuse loss of subcutaneous adipose tissue
Paradoxical respirationInward movement of the rib cage with inspiration (Hoover's
sign) in some patients"Pink puffers" are patients with predominant emphysema—
no cyanosis or edema, with decreased breath sounds."Blue bloaters" are patients with predominant bronchitis—
cyanosis and edema.Most patients have elements of each.
Systemic wastingSignificant weight lossBitemporal wastingDiffuse loss of subcutaneous adipose tissue
Paradoxical respirationInward movement of the rib cage with inspiration (Hoover's
sign) in some patients"Pink puffers" are patients with predominant emphysema—
no cyanosis or edema, with decreased breath sounds."Blue bloaters" are patients with predominant bronchitis—
cyanosis and edema.Most patients have elements of each.
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Advanced disease: signs of cor pulmonale
Elevated jugular venous distentionRight ventricular heaveThird heart soundHepatic congestionAscitesPeripheral edema
Elevated jugular venous distentionRight ventricular heaveThird heart soundHepatic congestionAscitesPeripheral edema
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Differential Diagnosis
1. Congestive heart failure2. Asthma3. Bronchiectasis4. Obliterative bronchiolitis5. Pneumonia6. Tuberculosis7. Atelectasis8. Pneumothorax9. Pulmonary embolism
1. Congestive heart failure2. Asthma3. Bronchiectasis4. Obliterative bronchiolitis5. Pneumonia6. Tuberculosis7. Atelectasis8. Pneumothorax9. Pulmonary embolism
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Considerations1. COLD is present only if chronic airflow obstruction
occurs.Chronic bronchitis without chronic airflow obstruction isnot COLD.
2. AsthmaReduced forced expiratory volume in 1 second (FEV1) inCOLD seldom shows large responses (>30%) to inhaledbronchodilators, although improvements up to 15% arecommon.Asthma patients can also develop chronic (not fullyreversible) airflow obstruction.
1. COLD is present only if chronic airflow obstructionoccurs.
Chronic bronchitis without chronic airflow obstruction isnot COLD.
2. AsthmaReduced forced expiratory volume in 1 second (FEV1) inCOLD seldom shows large responses (>30%) to inhaledbronchodilators, although improvements up to 15% arecommon.Asthma patients can also develop chronic (not fullyreversible) airflow obstruction.
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3. Problems other than COLD should besuspected when hypoxemia is difficult tocorrect with modest levels ofsupplemental oxygen.
4. Lung cancerClubbing of the digits is not a sign ofCOLD.In patients with COLD, development of lungcancer is the most likely explanation fornewly developed clubbing.
Considerations
3. Problems other than COLD should besuspected when hypoxemia is difficult tocorrect with modest levels ofsupplemental oxygen.
4. Lung cancerClubbing of the digits is not a sign ofCOLD.In patients with COLD, development of lungcancer is the most likely explanation fornewly developed clubbing.
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Diagnostic Approach
Initial assessment1. History and physical examination (Signs &
Symptoms)2. Pulmonary function testing to assess airflow
obstruction3. Radiographic studies
Initial assessment1. History and physical examination (Signs &
Symptoms)2. Pulmonary function testing to assess airflow
obstruction3. Radiographic studies
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Assessment of exacerbation1. History
FeverChange in quantity and character of sputumill contactsAssociated symptomsFrequency and severity of prior exacerbations
Assessment of exacerbation1. History
FeverChange in quantity and character of sputumill contactsAssociated symptomsFrequency and severity of prior exacerbations
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Assessment of exacerbation2. Physical examination
TachycardiaTachypneaChest examination
Focal findingsAir movementSymmetryPresence or absence of wheezingParadoxical movement of abdominal wallUse of accessory muscles
Perioral or peripheral cyanosisAbility to speak in complete sentencesMental status
Assessment of exacerbation2. Physical examination
TachycardiaTachypneaChest examination
Focal findingsAir movementSymmetryPresence or absence of wheezingParadoxical movement of abdominal wallUse of accessory muscles
Perioral or peripheral cyanosisAbility to speak in complete sentencesMental status
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3. Radiographic studiesChest radiography focal findings (pneumonia,atelectasis)
4. Arterial blood gasesHypoxemiaHypercapnia
5. Hospitalization recommended for:Respiratory acidosis and hypercarbiaSignificant hypoxemiaSevere underlying diseaseLiving situation not conducive to careful observationand delivery of prescribed treatment
3. Radiographic studiesChest radiography focal findings (pneumonia,atelectasis)
4. Arterial blood gasesHypoxemiaHypercapnia
5. Hospitalization recommended for:Respiratory acidosis and hypercarbiaSignificant hypoxemiaSevere underlying diseaseLiving situation not conducive to careful observationand delivery of prescribed treatment
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Laboratory TestsABG and oximetry
• Although not sensitive, they may demonstrateresting or exertional hypoxemia.
• Blood gases provide additional informationabout alveolar ventilation and acid–base statusby measuring arterial PCO 2 and pH.
Change in pH with PCO 2 is 0.08 units/10 mmHg acutelyand 0.03 units/10 mmHg in the chronic state.
Arterial pH allows classification of ventilatory failure,defined as PCO 2 > 45 mmHg, into an acute or chroniccondition.
• Although not sensitive, they may demonstrateresting or exertional hypoxemia.
• Blood gases provide additional informationabout alveolar ventilation and acid–base statusby measuring arterial PCO 2 and pH.
Change in pH with PCO 2 is 0.08 units/10 mmHg acutelyand 0.03 units/10 mmHg in the chronic state.
Arterial pH allows classification of ventilatory failure,defined as PCO 2 > 45 mmHg, into an acute or chroniccondition.
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Laboratory Tests1. Elevated hematocrit suggests chronic hypoxemia.2. Serum level of α1AT should be measured in some patients.
o Presenting at ≤ 50 years of ageo Strong family historyo Predominant basilar diseaseo Minimal smoking historyo Definitive diagnosis of α1AT deficiency requires PI type determination.
Typically performed by isoelectric focusing of serum, which reflects thegenotype at the PI locus for the common alleles and many of the rare PIalleles
Molecular genotyping can be performed for the common PI alleles (M, S,and Z).
3. Sputum gram stain and culture (for COLD exacerbation)
1. Elevated hematocrit suggests chronic hypoxemia.2. Serum level of α1AT should be measured in some patients.
o Presenting at ≤ 50 years of ageo Strong family historyo Predominant basilar diseaseo Minimal smoking historyo Definitive diagnosis of α1AT deficiency requires PI type determination.
Typically performed by isoelectric focusing of serum, which reflects thegenotype at the PI locus for the common alleles and many of the rare PIalleles
Molecular genotyping can be performed for the common PI alleles (M, S,and Z).
3. Sputum gram stain and culture (for COLD exacerbation)
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Imaging• Chest radiography
– Emphysema: obvious bullae, paucity ofparenchymal markings, or hyperlucency
– Hyperinflation: increased lung volumes,flattening of diaphragm
– Does not indicate chronicity of changes
• Chest CT– Definitive test for establishing the diagnosis of
emphysema, but not necessary to make thediagnosis
• Chest radiography– Emphysema: obvious bullae, paucity of
parenchymal markings, or hyperlucency– Hyperinflation: increased lung volumes,
flattening of diaphragm– Does not indicate chronicity of changes
• Chest CT– Definitive test for establishing the diagnosis of
emphysema, but not necessary to make thediagnosis
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Diagnostic ProceduresPulmonary function tests/spirometry
– Chronically reduced ratio of FEV1 to forced vitalcapacity (FVC)
• In contrast to asthma, the reduced FEV1 in COLD seldomshows large responses (>30%) to inhaled bronchodilators,although improvements up to 15% are common.
– Reduction in forced expiratory flow rates– Increases in residual volume– Increases in ratio of residual volume to total lung
capacity– Increased total lung capacity (late in the disease)– Diffusion capacity may be decreased in patients with
emphysema.Electrocardiography
– may detect signs of ventricular hypertroph
Pulmonary function tests/spirometry– Chronically reduced ratio of FEV1 to forced vital
capacity (FVC)• In contrast to asthma, the reduced FEV1 in COLD seldom
shows large responses (>30%) to inhaled bronchodilators,although improvements up to 15% are common.
– Reduction in forced expiratory flow rates– Increases in residual volume– Increases in ratio of residual volume to total lung
capacity– Increased total lung capacity (late in the disease)– Diffusion capacity may be decreased in patients with
emphysema.Electrocardiography
– may detect signs of ventricular hypertroph
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Classification
• GOLD stage• Classification based on pathologic type• GOLD stage• Classification based on pathologic type
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GOLD stage0
Severity: at riskSymptoms: chronic cough, sputum productionSpirometry: normal
ISeverity: mildSymptoms: with or without chronic cough or sputum productionSpirometry: FEV1:FVC < 0.7 and FEV1 ≥ 80% predicted
IISeverity: moderateSymptoms: with or without chronic cough or sputum productionSpirometry: FEV1:FVC < 0.7 and FEV1 50–80% predicted
IIISeverity: severeSymptoms: with or without chronic cough or sputum productionSpirometry: FEV1:FVC < 0.7 and FEV1 30–50% predicted
IVSeverity: very severeSymptoms: with or without chronic cough or sputum productionSpirometry:FEV1:FVC < 0.7 and FEV1 < 30% predicted orFEV1 < 50% predicted with respiratory failure or signs of right heart failure
0Severity: at riskSymptoms: chronic cough, sputum productionSpirometry: normal
ISeverity: mildSymptoms: with or without chronic cough or sputum productionSpirometry: FEV1:FVC < 0.7 and FEV1 ≥ 80% predicted
IISeverity: moderateSymptoms: with or without chronic cough or sputum productionSpirometry: FEV1:FVC < 0.7 and FEV1 50–80% predicted
IIISeverity: severeSymptoms: with or without chronic cough or sputum productionSpirometry: FEV1:FVC < 0.7 and FEV1 30–50% predicted
IVSeverity: very severeSymptoms: with or without chronic cough or sputum productionSpirometry:FEV1:FVC < 0.7 and FEV1 < 30% predicted orFEV1 < 50% predicted with respiratory failure or signs of right heart failure
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Classification based on pathologic type
Centriacinar emphysemaType most frequently associated with cigarette
smokingMost prominent in upper lobes and superior
segment of the lower lobes of the lungs
Panacinar emphysemaUsually observed in patients with α1AT
deficiencyMost prominent in lower lobes
Centriacinar emphysemaType most frequently associated with cigarette
smokingMost prominent in upper lobes and superior
segment of the lower lobes of the lungs
Panacinar emphysemaUsually observed in patients with α1AT
deficiencyMost prominent in lower lobes
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Treatment ApproachGeneral
– Institute therapy after assessment ofsymptoms, potential risks, costs, and benefits.
– Only 2 interventions have been demonstratedto influence the natural history.
Smoking cessationOxygen therapy in chronically hypoxemic
patients– All other current therapies are directed at
improving symptoms and decreasingfrequency and severity of exacerbations.
– Therapeutic response should determinecontinuation of treatment.
– Institute therapy after assessment ofsymptoms, potential risks, costs, and benefits.
– Only 2 interventions have been demonstratedto influence the natural history.
Smoking cessationOxygen therapy in chronically hypoxemic
patients– All other current therapies are directed at
improving symptoms and decreasingfrequency and severity of exacerbations.
– Therapeutic response should determinecontinuation of treatment.
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Exacerbation
• Assess the severity of both the acute andchronic components of the patient’sillness.
• Attempt to identify and treat the precipitantof the exacerbation.
• Assess the severity of both the acute andchronic components of the patient’sillness.
• Attempt to identify and treat the precipitantof the exacerbation.
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Specific TreatmentsStable-phase COLD, pharmacotherapy
Oxygen
1. Supplemental O2 is the only therapy demonstrated todecrease mortality.
2. In resting hypoxemia (resting O2 saturation < 88% or <90% with signs of pulmonary hypertension or right heartfailure), the use of O2 has been demonstrated tosignificantly affect mortality.
3. Supplemental O2 is commonly prescribed for patientswith exertional hypoxemia or nocturnal hypoxemia.
The rationale for supplemental O2 in these settings isphysiologically sound, but benefits are not well substantiated.
Oxygen
1. Supplemental O2 is the only therapy demonstrated todecrease mortality.
2. In resting hypoxemia (resting O2 saturation < 88% or <90% with signs of pulmonary hypertension or right heartfailure), the use of O2 has been demonstrated tosignificantly affect mortality.
3. Supplemental O2 is commonly prescribed for patientswith exertional hypoxemia or nocturnal hypoxemia.
The rationale for supplemental O2 in these settings isphysiologically sound, but benefits are not well substantiated.
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Specific TreatmentsStable-phase COLD, pharmacotherapy
Bronchodilators
– Used to treat symptoms– The inhaled route is preferred.– Side effects are less than with parenteral
delivery.– Theophyllline: various dosages and
preparations; typical dose 300–600 mg/d,adjusted based on levels
Bronchodilators
– Used to treat symptoms– The inhaled route is preferred.– Side effects are less than with parenteral
delivery.– Theophyllline: various dosages and
preparations; typical dose 300–600 mg/d,adjusted based on levels
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Specific TreatmentsStable-phase COLD, pharmacotherapy
Anticholinergic agents– Trial of inhaled anticholinergics is recommended in
symptomatic patients.– Side effects are minor.– Improve symptoms and produce acute improvement in
FEV– Do not influence rate of decline in lung function– Ipratropium bromide (short-acting anticholinergic)
(Atrovent)Inhaled: 30-min onset of action; 4-h durationAtrovent: metered-dose inhaler; 18 μg per inhalation; 1–2
inhalations qid
Anticholinergic agents– Trial of inhaled anticholinergics is recommended in
symptomatic patients.– Side effects are minor.– Improve symptoms and produce acute improvement in
FEV– Do not influence rate of decline in lung function– Ipratropium bromide (short-acting anticholinergic)
(Atrovent)Inhaled: 30-min onset of action; 4-h durationAtrovent: metered-dose inhaler; 18 μg per inhalation; 1–2
inhalations qid
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Specific TreatmentsStable-phase COLD, pharmacotherapy
• Tiotropium (long-acting anticholinergic)(Spiriva)
Spiriva: powder via handihaler; 18 μg perinhalation; 1 inhalation qd
• Symptomatic benefit• Long-acting inhaled β-agonists, such as
salmeterol, have benefits similar toipratropium bromide.
More convenient than short-acting agents
• Tiotropium (long-acting anticholinergic)(Spiriva)
Spiriva: powder via handihaler; 18 μg perinhalation; 1 inhalation qd
• Symptomatic benefit• Long-acting inhaled β-agonists, such as
salmeterol, have benefits similar toipratropium bromide.
More convenient than short-acting agents
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Specific TreatmentsStable-phase COLD, pharmacotherapy
• Addition of a β-agonist to inhaled anticholinergictherapy provides incremental benefit.– Side effects
TremorTachycardia
• Salmetrol (Serevent):Powder via diskus; 50-μg inhalation every 12 h
• Formoterol (Foradil):Powder via aerolizer; 12-μg inhalation every 12 h
• Addition of a β-agonist to inhaled anticholinergictherapy provides incremental benefit.– Side effects
TremorTachycardia
• Salmetrol (Serevent):Powder via diskus; 50-μg inhalation every 12 h
• Formoterol (Foradil):Powder via aerolizer; 12-μg inhalation every 12 h
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Albuterol (short-acting β-agonist) (ProventilHFA, Ventolin HFA, Ventolin, Proventil)
Metered-dose inhaler (or in nebulizersolution); 180-μg inhalation every 4–6 h asneeded
Combined β-agonist/anticholinergic:albuterol/ipratropium (Combivent)
Metered-dose inhaler (also available innebulizer solution); 120 mcg/21 μg perinhalation 1–2 inhalations qid
Specific TreatmentsStable-phase COLD, pharmacotherapy
Albuterol (short-acting β-agonist) (ProventilHFA, Ventolin HFA, Ventolin, Proventil)
Metered-dose inhaler (or in nebulizersolution); 180-μg inhalation every 4–6 h asneeded
Combined β-agonist/anticholinergic:albuterol/ipratropium (Combivent)
Metered-dose inhaler (also available innebulizer solution); 120 mcg/21 μg perinhalation 1–2 inhalations qid
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Inhaled glucocorticoids– Reduce frequency of exacerbations by 25–30%– No evidence of a beneficial effect for the regular use of
inhaled glucocorticoids on the rate of decline of lungfunction, as assessed by FEV1
– Consider a trial in patients with frequent exacerbations(≥2 per year) and those who demonstrate a significantamount of acute reversibility in response to inhaledbronchodilators.
– Side effectsIncreased rate of oropharyngeal candidiasisIncreased rate of loss of bone density
Specific TreatmentsStable-phase COLD, pharmacotherapy
Inhaled glucocorticoids– Reduce frequency of exacerbations by 25–30%– No evidence of a beneficial effect for the regular use of
inhaled glucocorticoids on the rate of decline of lungfunction, as assessed by FEV1
– Consider a trial in patients with frequent exacerbations(≥2 per year) and those who demonstrate a significantamount of acute reversibility in response to inhaledbronchodilators.
– Side effectsIncreased rate of oropharyngeal candidiasisIncreased rate of loss of bone density
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– Beclomethasone (QVAR):Metered-dose inhaler; 40–80 μg/spray; 40–160 μg bid
– Budesonide (Pulmicort):Powder via Turbuhaler; 200 μg/spray; 200 μg inhaled
bid– Fluticasone (Flovent):
Metered-dose inhaler; 44, 110 or 220 μg/spray; 88–440μg inhaled bid
– Triamcinolone (Azmacort)Metered-dose inhaler via built-in spacer; 100 μg/spray;
100–400 μg inhaled bid
Specific TreatmentsStable-phase COLD, pharmacotherapy
– Beclomethasone (QVAR):Metered-dose inhaler; 40–80 μg/spray; 40–160 μg bid
– Budesonide (Pulmicort):Powder via Turbuhaler; 200 μg/spray; 200 μg inhaled
bid– Fluticasone (Flovent):
Metered-dose inhaler; 44, 110 or 220 μg/spray; 88–440μg inhaled bid
– Triamcinolone (Azmacort)Metered-dose inhaler via built-in spacer; 100 μg/spray;
100–400 μg inhaled bid
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Specific TreatmentsStable-phase COLD, pharmacotherapy
Parenteral corticosteroids• Long-term use of oral glucocorticoids is not recommended.• Side effects
Osteoporosis, fractureWeight gainCataractsGlucose intoleranceIncreased risk of infection
• Patients tapered off long-term low-dose prednisone (~10mg/d) did not experience any adverse effect on thefrequency of exacerbations, quality of life, or lung function.
• On average, patients lost ~4.5 kg (~10 lb) when steroidswere withdrawn.
Parenteral corticosteroids• Long-term use of oral glucocorticoids is not recommended.• Side effects
Osteoporosis, fractureWeight gainCataractsGlucose intoleranceIncreased risk of infection
• Patients tapered off long-term low-dose prednisone (~10mg/d) did not experience any adverse effect on thefrequency of exacerbations, quality of life, or lung function.
• On average, patients lost ~4.5 kg (~10 lb) when steroidswere withdrawn.
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Theophylline• Produces modest improvements in expiratory
flow rates and vital capacity and a slightimprovement in arterial oxygen and carbondioxide levels in moderate to severe COPD
• Side effectsNausea (common)TachycardiaTremor
Specific TreatmentsStable-phase COLD, pharmacotherapy
Theophylline• Produces modest improvements in expiratory
flow rates and vital capacity and a slightimprovement in arterial oxygen and carbondioxide levels in moderate to severe COPD
• Side effectsNausea (common)TachycardiaTremor
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Other agents1. N-acetyl cysteine
Used for its mucolytic and antioxidant (currentclinical trials) properties
2. Intravenous α1AT augmentation therapy forpatients with severe α1AT deficiency
3. AntibioticsLong-term suppressive or "rotating" antibioticsare not beneficial
Specific TreatmentsStable-phase COLD, pharmacotherapy
Other agents1. N-acetyl cysteine
Used for its mucolytic and antioxidant (currentclinical trials) properties
2. Intravenous α1AT augmentation therapy forpatients with severe α1AT deficiency
3. AntibioticsLong-term suppressive or "rotating" antibioticsare not beneficial
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Smoking cessation• All patients with COLD should be strongly urged to quit
and educated about the benefit of cessation and risks ofcontinuation.
• Combining pharmacotherapy with traditional supportiveapproaches considerably enhances the chances ofsuccessful smoking cessation.
BupropionNicotine replacement (gum, transdermal, inhaler, nasal spray)The U.S. Surgeon General recommendation is for all smokers
considering quitting to be offered pharmacotherapy in theabsence of any contraindication.
Specific TreatmentsStable-phase COLD, nonpharmacologic therapies
Smoking cessation• All patients with COLD should be strongly urged to quit
and educated about the benefit of cessation and risks ofcontinuation.
• Combining pharmacotherapy with traditional supportiveapproaches considerably enhances the chances ofsuccessful smoking cessation.
BupropionNicotine replacement (gum, transdermal, inhaler, nasal spray)The U.S. Surgeon General recommendation is for all smokers
considering quitting to be offered pharmacotherapy in theabsence of any contraindication.
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General medical care1. Annual influenza vaccine2. Polyvalent pneumococcal vaccine is
recommended, although proof of efficacy inCOLD patients is not definitive.
Specific TreatmentsStable-phase COLD, nonpharmacologic therapies
General medical care1. Annual influenza vaccine2. Polyvalent pneumococcal vaccine is
recommended, although proof of efficacy inCOLD patients is not definitive.
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Pulmonary rehabilitation– Improves health-related quality of life,
dyspnea, and exercise capacity– Rates of hospitalization are reduced over 6 to
12 months.
Specific TreatmentsStable-phase COLD, nonpharmacologic therapies
Pulmonary rehabilitation– Improves health-related quality of life,
dyspnea, and exercise capacity– Rates of hospitalization are reduced over 6 to
12 months.
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Lung volume reduction surgeryProduces symptomatic and functional benefit in selected
patientsEmphysemaPredominant upper lobe involvement
ContraindicationsSignificant pleural disease (pulmonary artery systolic pressure
>45 mm Hg)Extreme deconditioningCongestive heart failureOther severe comorbid conditionsFEV1 < 20% of predicted and diffusely distributed emphysema
on CT or diffusing capacity for CO <20% of predicted (due toincreased mortality)
Specific TreatmentsStable-phase COLD, nonpharmacologic therapies
Lung volume reduction surgeryProduces symptomatic and functional benefit in selected
patientsEmphysemaPredominant upper lobe involvement
ContraindicationsSignificant pleural disease (pulmonary artery systolic pressure
>45 mm Hg)Extreme deconditioningCongestive heart failureOther severe comorbid conditionsFEV1 < 20% of predicted and diffusely distributed emphysema
on CT or diffusing capacity for CO <20% of predicted (due toincreased mortality)
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Lung transplantation• COLD is the leading indication.• Candidates
≤65 yearsSevere disability despite maximal medical therapyNo comorbid conditions, such as liver, renal, or
cardiac diseaseAnatomic distribution of emphysema and presence
of pulmonary hypertension are not contraindications.• Unresolved issues include whether single- or
double-lung transplantation is preferred.
Specific TreatmentsStable-phase COLD, nonpharmacologic therapies
Lung transplantation• COLD is the leading indication.• Candidates
≤65 yearsSevere disability despite maximal medical therapyNo comorbid conditions, such as liver, renal, or
cardiac diseaseAnatomic distribution of emphysema and presence
of pulmonary hypertension are not contraindications.• Unresolved issues include whether single- or
double-lung transplantation is preferred.
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Bronchodilators• Inhaled β-agonist, often with addition of an
anticholinergic agent• Frequency of administration depends on severity of
disease.• Initial treatment with nebulized therapy is common; it is
often easier to administer in older patients or those inrespiratory distress.
• Conversion to metered-dose inhalers is effective andallows an easier transition to outpatient care.
• Methylxanthines (e.g., theophylline) can be added to thisregimen, although proof of efficacy is lacking; serumlevels should be monitored to minimize toxicity
Specific TreatmentsExacerbations of COLD
Bronchodilators• Inhaled β-agonist, often with addition of an
anticholinergic agent• Frequency of administration depends on severity of
disease.• Initial treatment with nebulized therapy is common; it is
often easier to administer in older patients or those inrespiratory distress.
• Conversion to metered-dose inhalers is effective andallows an easier transition to outpatient care.
• Methylxanthines (e.g., theophylline) can be added to thisregimen, although proof of efficacy is lacking; serumlevels should be monitored to minimize toxicity
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Antibiotics• Choice should be based on local patterns
of antibiotic susceptibility of pathogensand the patient’s clinical condition.
Specific TreatmentsExacerbations of COLD
Antibiotics• Choice should be based on local patterns
of antibiotic susceptibility of pathogensand the patient’s clinical condition.
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Glucocorticoids• Have been demonstrated to reduce the length of
hospital stay, hasten recovery, and reduce thechance of subsequent exacerbation or relapsefor up to 6 months
• GOLD guidelines recommend 30–40 mg of oralprednisolone or its equivalent for 10–14 days.
• 2 weeks of glucocorticoid therapy producesbenefit indistinguishable from 8 weeks oftherapy.
• Side effects: hyperglycemia, particularly withpreexisting diagnosis of diabete
Specific TreatmentsExacerbations of COLD
Glucocorticoids• Have been demonstrated to reduce the length of
hospital stay, hasten recovery, and reduce thechance of subsequent exacerbation or relapsefor up to 6 months
• GOLD guidelines recommend 30–40 mg of oralprednisolone or its equivalent for 10–14 days.
• 2 weeks of glucocorticoid therapy producesbenefit indistinguishable from 8 weeks oftherapy.
• Side effects: hyperglycemia, particularly withpreexisting diagnosis of diabete
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OxygenSupplemental O2 should be supplied to
keep arterial saturation ≥90%.
Specific TreatmentsExacerbations of COLD
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Noninvasive positive pressure ventilationin patients with respiratory failure(PaCO2 > 45 mmHg)
Significantly reduces:MortalityNeed for intubationComplications of therapyLength of hospital stay
ContraindicationsCardiovascular instabilityImpaired mental status or inability to cooperateCopious secretions or inability to clear secretionsCraniofacial abnormalities or trauma precluding effective
fittingof mask
Extreme obesity
Specific TreatmentsExacerbations of COLD
Mechanical ventilatory supportNoninvasive positive pressure ventilation
in patients with respiratory failure(PaCO2 > 45 mmHg)
Significantly reduces:MortalityNeed for intubationComplications of therapyLength of hospital stay
ContraindicationsCardiovascular instabilityImpaired mental status or inability to cooperateCopious secretions or inability to clear secretionsCraniofacial abnormalities or trauma precluding effective
fittingof mask
Extreme obesity
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Invasive (conventional) mechanical ventilationvia endotracheal tube
IndicationsSevere respiratory distress despite initial therapyLife-threatening hypoxemiaSevere hypercapnia and/or acidosisMarkedly impaired mental statusRespiratory arrestHemodynamic instabilityOther complications
Goal: correct the aforementioned conditionsFor patients ≥ 65 years of age admitted to the intensive
care unit for treatment, mortality doubles over the next yearto 60%, regardless of whether mechanical ventilation wasrequired.
Specific TreatmentsExacerbations of COLD
Invasive (conventional) mechanical ventilationvia endotracheal tube
IndicationsSevere respiratory distress despite initial therapyLife-threatening hypoxemiaSevere hypercapnia and/or acidosisMarkedly impaired mental statusRespiratory arrestHemodynamic instabilityOther complications
Goal: correct the aforementioned conditionsFor patients ≥ 65 years of age admitted to the intensive
care unit for treatment, mortality doubles over the next yearto 60%, regardless of whether mechanical ventilation wasrequired.
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Monitoring• Symptom assessment• Pulse oximetry• Serial pulmonary function tests
Specific TreatmentsExacerbations of COLD
Monitoring• Symptom assessment• Pulse oximetry• Serial pulmonary function tests
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Complications• Cor pulmonale
Right ventricular hypertrophy and failure inducedby hypoxia
• Spontaneous pneumothorax occurs in asmall proportion of emphysematouspatients.
Specific TreatmentsExacerbations of COLD
Complications• Cor pulmonale
Right ventricular hypertrophy and failure inducedby hypoxia
• Spontaneous pneumothorax occurs in asmall proportion of emphysematouspatients.
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• The principal determinant of morbidity inCOLD is the degree of airway obstruction.– Patients who continue to smoke cigarettes
experience a yearly decrease in FEV1 of 80–100 mL.
– Even for patients who quit smoking, the FEV1decreases by 30 mL per year.
• Median survival for severe disease (FEV1< 1 L) is 4 years.
Prognosis
• The principal determinant of morbidity inCOLD is the degree of airway obstruction.– Patients who continue to smoke cigarettes
experience a yearly decrease in FEV1 of 80–100 mL.
– Even for patients who quit smoking, the FEV1decreases by 30 mL per year.
• Median survival for severe disease (FEV1< 1 L) is 4 years.
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Prevention
• Smoking prevention or cessation• Prevention of exacerbations
– Long-term suppressive antibiotics are not beneficial.– Inhalation glucocorticoids should be considered in
patients with frequent exacerbations or in patientswith an asthmatic component.
• Vaccination against influenza and pneumococcalinfection
• Smoking prevention or cessation• Prevention of exacerbations
– Long-term suppressive antibiotics are not beneficial.– Inhalation glucocorticoids should be considered in
patients with frequent exacerbations or in patientswith an asthmatic component.
• Vaccination against influenza and pneumococcalinfection
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PEARL
Dyspnea with arm work, especially abovethe shoulder, is particularly common and
severe in COLD.
Dyspnea with arm work, especially abovethe shoulder, is particularly common and
severe in COLD.
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