A. Patient with Established Diagnosis of COPD - Chronic obstructive pulmonary disease (COPD) is defined by the American Thoracic Society (ATS) in Standards for the Diagnosis and Care of Patients with Chronic Obstructive Pulmonary Disease (1995). Further detail on lung function testing is found in another ATS publication (1991).
b. Chronic bronchitis is defined as the presence of chronic productive cough for 3 months of each of two successive years in a patient in whom other causes of chronic cough have been excluded.
c. Emphysema is defined as abnormal permanent enlargement of the airspaces distal to the terminal bronchioles, accompanied by destruction of their walls and without obvious fibrosis.
d. Asthma is by definition associated with reversible airflow obstruction. Patients with asthma whose airflow obstruction is completely reversible are not considered to have COPD. The obstruction in many patients with COPD may include a significant reversible component. Some patients with asthma may develop irreversible airflow obstruction indistinguishable from COPD.
B. Perform Clinical Assessment, History, Physical Examination, Lab Tests, and Spirometry
b. Environmental (chronological) - May disclose important risk factors
c. Cough (chronic, productive) - Frequency and duration, whether or not productive (especially on awakening)
d. Wheezing
e. Acute chest illnesses - Frequency, productive cough, wheezing, dyspnea, fever
f. Dyspnea
2. Physical Examination of Chest
b. Severe emphysema indicated by:
c. Severe disease suggested by (characteristics not diagnostic):
3. Other - Unusual positions to relieve dyspnea at rest, digital clubbing (suggests possibility of lung cancer or bronchiectasis), and mild dependent edema that may be seen in absence of right heart failure
4. Laboratory
b. Spirometry (pre- and postbronchodilation)Essential to confirm presence and reversibility of airflow obstruction and to quantify maximum level of ventilatory function (ATS 1995)
c. Lung volumesMeasurement of more than forced vital capacity is not necessary except in special circumstances (e.g., presence of giant bullae)
d. Carbon monoxide diffusing capacityUnnecessary except in special instances (e.g., dyspnea out of proportion to severity of airflow limitation)
e. Arterial blood gases are not needed in staged mild disease, but remain the standard for determining the need for oxygen therapy
f. Alpha1-antitrypsin (AAT)AAT deficiency accounts for less than 1 percent of COPD. Obtain a serum AAT level to screen for AAT deficiency in the following situations:
| Severity | FEV1 ** Percent Predicted |
| Mild | 50 to < 79 |
| Moderate | 35 to 49 |
| Severe | < 35 |
| Intervention | References | Grade of Evidence | Strength of Recommendation |
| Definition of COPD | ATS 1991, 1995
ERS, Siafakas 1995 |
C | 1 |
| Staging | ATS 1995
ERS, Siafakas 1995 |
C | 1 |
D. Acute Exacerbation of COPD - Acute exacerbation is defined as a recent deterioration of the patient's clinical and functional state that is due to worsening of their COPD. Typical symptoms and signs of COPD exacerbation are listed below (adapted from the European Respiratory Society Consensus Statement, Siafakas 1995).
E. Are Symptoms Optimal for Patient Since Last Visit (Symptoms on Usual Daily Activities)? - Client may exhibit symptoms of dyspnea and/or wheezing. Dyspnea may be at rest or disproportionate to the degree of breathlessness expected for a given activity.
F. Does Patient Have Symptoms of Apnea?
| Intervention | References | Grade of Evidence | Strength of Recommendation |
| COPD patients do not normally have EDS, even with nocturnal desaturation. | Orr 1990 | C | 2a |
2. Pneumoccocal Vaccination is Recommended - The Advisory Committee on Immunization Practices (CDC 1997) recommends vaccination for all patients with COPD and emphysema. Patients age less than 65 who were vaccinated or more than 5 years previously should be revaccinated. When the status of previous vaccination is unsure, vaccination is indicated.
However, the evidence for the efficacy of pneumococcal vaccination in patients with COPD is inconclusive. One small randomized controlled trial failed to demonstrate vaccine efficacy for pneumococcal infection-related or other medical outcomes in the heterogeneous group of subjects labeled as high-risk. Case-controlled trials suggest an effectiveness of 65 to 84 percent among high-risk patients that have included those with COPD.
3. Annual Influenza Vaccination - Annual influenza vaccination is recommended for individuals with chronic pulmonary disease unless contraindications due to severe anaphylactic hypersensitivity to egg protein. Influenza vaccination has been shown to be 30 to 80 percent effective in preventing illness, complications, and death in high-risk populations. Pneumococcal and influenza vaccines can be administered concurrently at different sites without increasing side effects.
Patients with COPD should avoid environmental exposures that exacerbate their symptoms (e.g., occupational exposures, second-hand smoke, air pollution).
| Intervention | References | Grade of Evidence | Strength of Recommendation |
| Pneumococcal vaccination.
Most studies show an advantage but one small, randomized, placebo-controlled trial did not. |
CDC ACIP 1997
Fine 1994 Shapiro 1984, 1991 Farr 1995 Sims 1988 Forrester 1987 Simberkoff 1986 |
C
|
2a
|
| Annual influenza vaccination. | CDC ACIP 1997
Govaert 1994 Nichol 1994 Gross 1988 Fedson 1993 Foster 1992 |
C | 1 |
| Smoking cessation slows lung function decline. | Anthonison 1994
Xu 1992 Camilli 1987 Fletcher 1977 |
A | 1 |
5. Pulmonary Rehabilitation--Referrals are indicated in patients on optimal medical therapy and who:
| Intervention | References | Grade of Evidence | Strength of Recommendation |
| Nutritional counseling | ATS 1995
Wilson 1986 |
C | 2b |
| Pulmonary rehabilitation | Goldstein 1994
ATS 1995 |
B | 2a |
H. Be Aware of Precautions and Recommendations for Use of Medications and Aerosols
b. Use spacers to improve compliance.
c. Avoid overuse; check number of metered dose inhalers (MDIs) used per month against number of puffs per MDI (200 to 300+, depending on brand).
d. Instruct client on maximum number of puffs per day (usually 8 to 12) and on number allowed during an exacerbation (e.g., 12 to 24 over 3 to 4 hours) before additional intervention is required.
e. If a long-acting agent is used, caution client that frequent use must be avoided.
f. Home updraft nebulizers with inhalant solutions providing large dosages
are rarely needed.
b. Reduce dosage if drug clearance is likely to be impaired because of illness, liver malfunction, or concomitant drugs.
c. Do not allow any additional theophylline preparation to be taken.
d. Drug must be taken at the same time each day with respect to meals.
e. When symptoms change, acute illness develops, new drugs are added, or symptoms suggestive of toxicity develop, check serum level of theophylline.
f. Aim for a serum level of 5 to 12 g/ml; adjust dosage and follow serum
level when indicated.
b. Be prepared to increase dose if necessary from 2 to 3 puffs 3 to 4 times a day to 6 to 8 puffs 3 to 4 times a day, if tolerated.
c. Caution client that onset of effect is relatively slow; additional doses should not be taken for acute symptom relief.
d. Monitor for side effects, e.g., tachycardia, dry mouth, glaucoma, prostatism, or bladder neck obstruction.
b. Monitor for hypertension, diabetes, weight gain, mental changes, infections, central polar cataracts, skin thinning, purpura, osteoporosis, and osteonecrosis.
c. Distinguish psychological benefit from true pulmonary benefit by following forced expiratory volume in 1 second (FEV1) for 2 weeks after initiating therapy.
d. Administer prophylactic calcium therapy to women; treat osteoporosis appropriately.
e. Steroid-dependent clients require steroid coverage during any crisis for many months after stopping steroids.
f. Repeatedly evaluate client to determine whether steroid therapy can
be discontinued.
b. Use a spacer; monitor for oral thrush and laryngeal dysfunction.
c. Be aware that aerosol steroid side effects may occur in skin, bone, etc.
d. When introducing aerosol steroids in a client on an oral steroid, wean slowly off the oral drug.
| Intervention | References | Grade of Evidence | Strength of Recommendation |
| Precautions when using pharmacotherapy | ATS 1995 | C | 1 |
7. Recommendation - MDI with, if necessary, a spacer is preferred unless not recommended by manufacturer; a hand-held nebulizer should be used only if client unable to use an MDI.
Nebulizers generally require between 2 and 12 times as much inhaled beta2-agonist to produce the same effect as an MDI, depending on the nebulizer used. Adherence with nebulizers is similar to that with MDI. There is no obvious advantage in using a nebulizer in a stable COPD client who can properly use an MDI.
| Intervention | References | Grade of Evidence | Strength of Recommendation |
| 52 percent used MDI once or less daily rather than the required three times daily. | Rand 1995 | C | 1 |
| Adherence with intermittent positive pressure breathing (IPPB) or nebulizers was 50.6 percent. | Turner 1995 | C | 1 |
| Maximum bronchodilation similar between nebulizer and MDI beta2-agonist. Nebulizer dose twice MDI dose to produce same effect. | Mestitz 1989 | B | 1 |
| Dose of nebulized albuterol producing the same bronchodilation in any of peak expira-tory flow rate, FEV1, or forced vital capacity was about 10 times higher than with MDI. | Jenkins 1987 | B | 1 |
| No difference in outcome between nebulizer and MDI. Nebulized metaproterenol dose was about seven times higher than with the MDI. | Turner 1988 | B | 1 |
| It takes about 12.5 times as much nebulized albuterol to achieve the same increase in FEV1 as with an MDI. | Harrison 1983 | B | 1 |