Frontline Treatment of COPD
Management of Stable COPD
The careful management of COPD in the outpatient setting can effectively
improve symptoms, minimize deterioration in pulmonary function,
and prevent hospitalization during acute exacerbations. There are
four phases in the primary care physician's strategy to meet these
goals:
- Stress smoking cessation and patient education about the disease.
- Improve pulmonary function as much as possible by treating
any reversible component of the patient's lung disease and by
establishing a therapeutic “plateau” to prevent accelerated
deterioration in pulmonary function as the patient grows older.
- Treat acute exacerbations of COPD in the outpatient setting.
- Prevent non-COPD complications of therapy.
Phase
1 - Smoking Cessation and Patient Education
The primary care physician is in an ideal position to emphasize
the importance of smoking cessation to all patients, but especially
those with early or moderately advanced COPD. Educate your patients
about the damaging effect of tobacco smoke on the progression of
the disease process and on the worsening of their pulmonary function.
Explain to patients that when they stop smoking they will reap many
benefits, including reduced airway secretions, reduced airway inflammation,
and reduced bronchospasm.
It helps to discuss the importance of behavior modification and
smoking addiction. Frequently, a patient is receptive to their physician’s
recommendation about a nicotine patch or referral to a smoking cessation
class. It is important to schedule follow-up visits in the clinic
to reinforce the patient's decision to quit smoking
(See Section J).
In addition, educating the patient and his or her family about
COPD, the importance of complying with medication regimens, and
the value of exercise is vital to the successful management of the
disease.
The most useful approach to smoking cessation is counseling that
quitting is absolutely essential. Picking a quit date is key to
the entire process. A variety of pharmacologic agents are available
to mitigate nicotine withdrawal symptoms. These are summarized in
Table 2.
Table
2: Drugs Used for Smoking Cessation
| Drug and Method of Administration |
Unit Dose |
Dose Interval |
| Nicotine polacrilex (oral) |
2 to 4 mg |
Every 1 to 2 hours* |
| Transdermal nicotine patch |
21, 14, and 7 mg
15, 10, and 5 mg
22 and 11 mg |
Over 24 hours
Over 16 hours
Over 24 hours |
| Nasal nicotine spray |
0.5 mg/inhalation/nostril |
8 to 40 mg/day in hourly or p.r.n. dosing |
| Nicotine inhaler |
10 mg/inhaler |
Inhale for 20 minutes 6 to 16 times/day |
| Bupropion sustained- release tablets |
150 mg |
150 mg for 3 days, then 300 mg/day |
| Buspirone tablets |
15, 10, and 5 mg |
7.5 mg b.i.d., starting dose; 60 mg/day, maximum dose |
| * Fifteen to 30 pieces may be
chewed over 24 hours. |
When nicotine replacement is chosen, it should be started on the
quit date. The advantage of the gum is that it allows the patient
to titrate the rate of nicotine absorption. Four mg gum is more
effective than 2 mg gum in patients who are most heavily addicted,
i.e., smoking more than one pack a day, and beginning early in the
morning, with the morning cigarette being the most important. When
bupropion is given, it should be initiated approximately one week
before the quit date. The nicotine products can be used in combination.
Even if used together in full manufacturers’ doses, it is
unlikely that nicotine blood levels will exceed those produced regularly
by the addicted smoker. A combination of nicotine replacement and
bupropion has resulted in the highest success in biologically proven
cessation one year after initiation of therapy.
References
Hankinson JL, Odencrantz JR, Fedan KB. Spirometric reference values
from a sample of the general U.S. population. Am J Respir Crit Care
Med 1999;159:179-187. An updated review. The fev6 is a good surrogate
marker of fvc and the fev1/fev6 ratio is useful in identifying subjects
with rapid rates of decline in fev.
Hilleman DE, Mohiuddin SM, Del Core MG, Sketch MH Sr. Effect of
buspirone on withdrawal symptoms associated with smoking cessation.
Arch Intern Med 1992;152:350-352. This non-benzodiazepine was effective
in reducing the symptoms of nicotine withdrawal.
Hurt RD, Dale LC, Fredrickson PA, et al. Nicotine patch therapy
for smoking cessation combined with physician advice and nurse follow-up.
One-year outcome and percentage of nicotine replacement. jama 1994;271:595-600.
This randomized trial showed that the nicotine patch increased smoking
cessation more than physician advice and nurse follow-up.
Hurt RD, Sachs DP, Glover ED, et al. A comparison of sustained-release
bupropion and placebo for smoking cessation. N Engl J Med 1997;337:1195-1202.
This randomized clinical trail demonstrated the effectiveness of
bupropion compared with placebo.
Jorenby DE, Keehn DS, Fiore MC. Comparative efficacy and tolerability
of nicotine replacement therapies. CNS Drugs. 1995;3:227-236. A
review of the effectiveness of drugs used in nicotine withdrawal.
Jorenby DE, Leischow SJ, Nides MA, et al. A controlled trial of
sustained-release bupropion, a nicotine patch, or both for smoking
cessation. N Engl J Med 1999; 340:685-691. A greater quit rate was
achieved with combined therapy compared with either agent used separately.
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