Role Of History, Physical Examination, Laboratory Studies

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Differentiating Asthma from COPD: Role of History, Physical Examination, Laboratory Studies, and Lung Function Testing Stephen P Peters, MD, PhD, FAAAAI Professor of Medicine, Pediatrics and Translational Science Associate Director, Center for Genomics and Personalized Medicine Research

Transcript of Role Of History, Physical Examination, Laboratory Studies

Page 1: Role Of History, Physical Examination, Laboratory Studies

Differentiating Asthma from COPD: Role of History, Physical Examination,

Laboratory Studies, and Lung Function Testing

Stephen P Peters, MD, PhD, FAAAAIProfessor of Medicine, Pediatrics and Translational ScienceAssociate Director, Center for Genomics and Persona lized

Medicine Research

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Objectives and Disclosure

� Objective: To review the role of History, Physical Examination, Laboratory Studies, and Lung Function Testing in distinguishing Asthma from COPD (Emphysema and Chronic Bronchitis)

� Disclosure: Nothing to disclose for this topic

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Program - Parts 2 and 3

� Dr. Bateman - Why Differentiating Asthma from COPD is Important

� Dr. Al Ameri - Case Studies in Asthma and COPD

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Discussion Question - 1

� We are all taught that the Medical History, Physica l Examination, Laboratory Tests, and Specialized Test s are all important part of a medical evaluation.

True or False

� Certain elements of the Medical History and/or Physical Examination are not only helpful but are ESSENTIAL for making the correct diagnosis of asthma versus COPD?

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Key Elements of History

� Symptoms

� Dyspnea, Dyspnea at Rest or on Exertion, Cough, Chest Tightness, Wheezing

� Onset of Symptoms – Childhood vs Adult

� Precipitating Events for Symptoms

� Associated Conditions – Rhinitis, Sinusitis, GERD, h/o Pneumonia, Bronchitis

� Exposures – Cigarettes, Environmental, Work

� Family History – Atopic Disorders, COPD, Cigarette-Related Illnesses

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Discussion Question - 1

Certain elements of the Medical History and/or Phys ical Examination are not only helpful but are ESSENTIALfor making the correct diagnosis of asthma versus COPD?

TRUEChronic Bronchitis - Clinical, Historical Diagnosis

Cough productive of sputum

….. most days of the week

….. at least 3 months per year

….. for at least 2 years

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Role of Physical Examination

� Major - Attempt to confirm to presence of airway obstruction (airflow limitation)

� Wheezing, Prolonged Expiration, Decreased Breath Sounds, Rhonchi

� Minor - Search for Ancillary Findings

� Allergic Shiners, Nasal Crease

� Clubbing, Cyanosis, Yellow Fingers, Cachexia

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Discussion Question 2

�What other disorders are associated with airway obstruction?

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Other Diseases Which Could Present with Airflow Limitation

� Bronchiectasis

� Cystic Fibrosis

� Tumors [Laryngeal, Tracheal]

� Tracheomalacia

� Endobronchial Diseases

�Sarcoidosis

�Amyloidosis

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Discussion Question 3

� What is the major role of laboratory and radiologic testing in Asthma and COPD?

� What tests might be unusually informative?

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Discussion Question 3

� What is the major role of laboratory and radiologic testing in Asthma and COPD?� To rule out other disease entities

� To suggest atypical variants of these diseases

� What tests might be unusually informative?� CXR/CT Chest – R/O Interstitial Processes, Lower

Lobe Emphysema [ αααα-1-AT]� Total IgE - Very high (>1000) [ABPA]

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Discussion Question 3

� Can spirometery alone always differentiate Asthma from COPD?

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Simplified Algorithm – PFT Interpretation

Pellegrino, et al. Eur Respir J 2005; 26:948–968

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Diagnosing Airway Obstruction (Airflow Limitation)

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Types of Ventilatory Defects and Their Diagnoses

Obstruction� FEV1/VC <5th percentile of predicted� A decrease in flow at low lung volume is not specif ic for small airway disease in individual patients

� A concomitant decrease in FEV1 and VC is most commo nly caused by poor effort, but may rarely reflect airflow obstruction. Confirmation of airway obstruction requires measurement of lung volumes

� Measurement of absolute lung volumes may assist in the diagnosis of emphysema, bronchial asthma and chronic bronchitis. It may also be usefu l in assessing lung hyperinflation

� Measurements of airflow resistance may be helpful i n patients who are unable to perform spirometric manoeuvres

Restriction� TLC <5th percentile of predicted� A reduced VC does not prove a restrictive pulmonary defect. It may be suggestive of lung restriction

when FEV1/VC is normal or increased

� A low TLC from a single-breath test should not be s een as evidence of restriction

Mixed� FEV1/VC and TLC <5th percentile of predicted

Pellegrino, et al. Eur Respir J 2005; 26:948–968

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Distinguishing Asthma (Chronic Bbronchitis) from Emphysema

Pellegrino, et al. Eur Respir J 2005; 26:948–968

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Severity of Spirometric Abnormality

Degree of severity FEV1 % pred

Mild >70

Moderate 60–69

Moderately severe 50–59

Severe 35–49

Very severe <35

Pellegrino, et al. Eur Respir J 2005; 26:948–968

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NHLBI: Classifying Severity for Patients ( ≥12 Years of Age) Not Currently Taking Long-Term Control

Medications

NHLBI Guidelines 2007.

Persistent

Moderate SevereMild

Classification of Asthma Severity (youths ≥12 y of age and adults)

Intermittent

≤2 d/wk

≤2x/mo

≤2 d/wk

None

• Normal FEV1between

exacerbations

• FEV1 >80% predicted

• FEV1/FVC normal

• FEV1 <80% predicted

• FEV1/FVC normal

• FEV1 >60% but<80% predicted• FEV1/FVC reduced 5%

• FEV1 <60% predicted

• FEV1/FVC reduced >5%

Minor limitation Some limitation Extremely limited

>2 d/wkbut not>1 x/d

DailySeveral times

per day

3–4x/mo >1x/wk but not nightly

Often 7x/wk

>2 d/wkbut not daily

Daily Throughout the day

Interference with

normal activity

SABA use for symptom control (not prevention of

EIB)

Nighttimeawakenings

Symptoms

Lung function

Impairment

Normal FEV1 / FVC:

8-19 y 85%

20-39 y 80%

40-59 y 75%

60-80 y 70%

Risk Exacerbationsrequiring oral systemic

corticosteroidsRelative annual risk of exacerbations may be related to FEV1.

Consider severity and interval since last exacerbation. Frequency and severity may fluctuate over time for patients in any severity category.

0-2/y > 2/y

Components of Severity

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Spirometry to Assess COPD Severity and Progression: GOLD Guidelines 1,2

1. American Thoracic Society, European Respiratory Society. Standards for the diagnosis and management of patients with COPD.http://www.thoracic.org/sections/copd/. Accessed No vember 19, 2008.

2. Global Initiative for Chronic Obstructive Lung D isease. Global strategy for diagnosis, management, and prevention of chronic obstructivepulmonary disease. Updated 2008. http://www.goldc opd.com/Guidelineitem.asp?l1=2&l2=1&intId=989. Acce ssed November 21, 2008.

I II III IV

�FEV1/FVC <0.70

�FEV1 ≥80% predicted

�FEV1/FVC <0.70

� 50% ≤ FEV1 <80% predicted

�FEV1/FVC <0.70

� 30% ≤FEV1<50% predicted

�FEV1/FVC <0.70

�FEV1 <30% predicted orFEV1 <50% predicted plus chronic respiratory failure

Chronic cough and sputum production

Stage I symptoms+ dyspnea

Progressive dyspnea

Stage III symptoms + respiratory failure, right heart failure, weight loss, arterial hypoxemia

Stage

Severity

Typicalsymptoms

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Flow Volume Curves

Moderate Airflow Limitation

Normal

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Normal Variable extra-thoracic upper airway obstruction .

Flow Volume Curves

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Simplified Algorithm – PFT Interpretation

Pellegrino, et al. Eur Respir J 2005; 26:948–968

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Considerations for SeverityClassification

� The severity of pulmonary function abnormalities is based on FEV1 % pred. This does not apply to upper airway obstruction. In addition, it might not be suitable for comparing different pulmonary diseases or conditions.

� FEV1 may sometimes fail to properly identify the severity of a defect, especially at the very severe stages of the diseases.

� FEV1 % pred correlates poorly with symptoms and may not, by itself, accurately predict clinical severit y or prognosis for individual patients.

� Lung hyperinflation and the presence of expiratory flow limitation during tidal breathing may be useful in categorising the severity of lung function impairme nt.

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Pellegrino, et al. Eur Respir J 2005; 26:948–968