Background: Chronic obstructive pulmonary disease (COPD), usually caused by tobacco smoking, is one of the leading causes of morbidity and mortality. Smoking cessation at an early stage of the disease usually stops further progression. A study was undertaken to determine if diagnosis of airway obstruction was associated with subsequent success in smoking cessation, as advised by a physician.
Methods: 4494 current smokers (57.4% men) with a history of at least 10 pack-years of smoking were recruited from 100 000 subjects screened by spirometric testing for signs of airway obstruction. At the time of screening all received simple smoking cessation advice. 1177 (26.2%) subjects had airway obstruction and were told that they had COPD and that smoking cessation would halt rapid progression of their lung disease. No pharmacological treatment was proposed. After 1 year all subjects were invited for a follow up visit. Smoking status was assessed by history and validated by exhaled carbon monoxide level.
Results: Nearly 70% attended a follow up visit (n = 3077): 61% were men, mean (SD) age was 52 (10) years, mean (SD) tobacco exposure 30 (17) pack-years, and 33.3% had airway obstruction during the baseline examination. The validated smoking cessation rate in those with airway obstruction was 16.3% compared with 12.0% in those with normal spirometric parameters (p = 0.0003). After correction for age, sex, nicotine dependence, number of cigarettes smoked daily, and lung function, success in smoking cessation was predicted by lower lung function, lower nicotine dependence, and lower tobacco exposure.
Conclusions: Simple smoking cessation advice combined with spirometric testing resulted in good 1 year cessation rates, especially in subjects with airway obstruction.
- CO, carbon monoxide
- COPD, chronic obstructive pulmonary disease
- FEV1, forced expiratory volume in 1 second
- FTND, Fagerström test for nicotine dependence
- FVC, forced vital capacity
- lung function testing
- smoking cessation
- chronic obstructive pulmonary disease
Statistics from Altmetric.com
- CO, carbon monoxide
- COPD, chronic obstructive pulmonary disease
- FEV1, forced expiratory volume in 1 second
- FTND, Fagerström test for nicotine dependence
- FVC, forced vital capacity
Chronic obstructive pulmonary disease (COPD) is one of the leading causes of morbidity and mortality worldwide and is increasing in prevalence.1 In the United States, between 1966 and 1995 age adjusted death rate for stroke and coronary artery disease declined by 58% and 45% respectively,2 whereas the death rate from COPD increased by 71%1 making it the fourth leading cause of death. Direct annual costs for COPD in the US were estimated to be over $18 billion,3 and the economic impact of work loss accounted for an additional $10 billion.4 The morbidity and mortality from cardiovascular diseases have been successfully reduced over the last 40 years as a result of effective preventive measures. However, the concurrent failure of pharmacological treatment to affect the increasing death rates from COPD should encourage new methods to be sought to reverse this trend.5
Tobacco smoke is the main cause of COPD, responsible for 85–90% of all cases.6,7 Smoking cessation at an early stage of the disease has been proved to slow down the decline in forced expiratory volume in 1 second (FEV1) to that observed in healthy subjects.8,9 The diagnosis of COPD at an early stage of the disease may be done by performing spirometric tests in smokers using case finding10 or population screening11 methods. We hypothesised that the diagnosis of smoking related lung disease would increase the efficacy of smoking cessation advice in affected subjects. The aim of this study was to compare the effects of spirometric tests combined with simple smoking cessation advice on rates of smoking cessation in two groups of subjects—those with airway obstruction and those with normal spirometric parameters.
Investigations were performed as part of the National Program of Early Diagnosis and Prevention of COPD in Poland.11 The National Program was introduced to promote early diagnosis and secondary prevention of COPD. Written materials were disseminated for local TV, radio and journals. Special posters and leaflets were displayed in healthcare facilities. Materials included information on causes and symptoms of COPD. In some places it was felt that the term “COPD” was unfamiliar and was replaced by a better known term “emphysema”. Information that not all smokers are susceptible to COPD and that a spirometric test is a simple non-invasive method to detect COPD at an early stage of the disease were also included. Smokers aged 40+ years with a history of at least 10 pack-years were invited to outpatient chest clinics all over the country for a free breathing test. However, all subjects who visited the clinic for spirometric tests—whether younger than 40 years of age or non-smokers—were also accepted. All investigated subjects were volunteers responding to the offer of free spirometric tests and smoking cessation counselling. No patients with chronic chest diseases were included in the study. Screening clinics were held on Saturday mornings and during the late afternoon on working days, facilitating fully employed subjects to attend the test. Outpatient chest clinics are usually located in a town centre with easy access to public transportation.
Simple spirometric tests with measurements of forced vital capacity (FVC) and FEV1 were performed by registered nurses trained in spirometric testing at the lung function laboratory of a chest hospital. Training was completed with an examination and certificate. A few of the technologists attended a high school for medical technicians where spirometric testing is part of the curriculum. Spirometric tests were performed in accordance with American Thoracic Society guidelines.12 Predicted spirometric values of ECCS/ERS were used.13 Following the 1995 ERS guidelines,14 the presence of airway obstruction was defined as an FEV1/FVC <88% predicted, and the severity of the impairment was classified using FEV1 percentage predicted as follows: >70% mild, 50–69% moderate, <50% severe.
The physician in charge of the National Program discussed the results of the spirometric tests with each subject, relating the results to his/her smoking habit. The subject’s percentage predicted FEV1 value was superimposed on a simplified Fletcher’s diagram,15 showing the relationship of the actual result with the predicted value for age and the expected subsequent FEV1 decline in future if the subject continued to smoke (fig 1). All participants were strongly encouraged to stop smoking and received a smoking cessation booklet to take home. This booklet provided information on the harmful effects of tobacco smoke, the positive health and economic effects of smoking cessation, and useful hints on how to stop smoking. Smoking cessation advice and discussion on the breathing test result took an average of 5–7 minutes. No pharmacological treatment of smoking addiction was offered. Nicotine replacement therapy was available over the counter in Poland at the time of this project; however, nicotine replacement gum, patches and inhalers are not reimbursed and are rather expensive. In subjects with normal spirometric parameters, smoking cessation advice was focused on the risk of developing COPD, lung cancer, coronary artery disease, and the harmful effects of smoke to family members. Fletcher’s diagram was also shown.
A total of 110 000 subjects were screened in the Program.11 Ten of the 60 chest clinics taking part in the Program with the highest number of subjects enrolled in different regions of the country were chosen to assess the effects of the smoking cessation advice 1 year after the initial visit. Subjects screened at centres selected for the study did not differ from those in the remaining centres in terms of sex (58.6% v 58.0% male), nicotine dependence (4.73 v 4.76 Fagerström Test for Nicotine Dependence (FTND) points), and severity of airflow limitation (FEV1 % predicted 89.95 (23.5) v 86.79 (27.4)). There was a statistically significant difference between subjects in the selected and the remaining centres in age (54.2 (12.3) v 53.3 (11.3) years), age at smoking initiation (19.9 (5.0) v 20.3 (5.2) years), number of cigarettes smoked daily (19.5 (9.9) v 18.9 (9.4)), and cumulative exposure to tobacco smoke (30.1 (19.3) v 28.7 (18.7) pack-years), respectively. However, because of the very large number of subjects included (n = 110 000), these differences were not considered clinically significant.
During the years 2000–2001, 4494 current smoking adults attended the Program at the clinics chosen: 2580 men (57.4%) and 1914 women (42.6%). From this group, 26.2% were found to have airway obstruction: 7.5% mild, 13.5% moderate, and 5.2% severe. The remaining 73.8% either had normal spirometric parameters or mild reductions in FVC without airway obstruction.
A letter of invitation for a follow up visit was mailed to all subjects of the group during the 11th month following the initial visit. In five centres the letter of invitation was resent after 1 month if the invited person had not responded. Some of the subjects (13.2%) were invited for follow up by a telephone call. In one centre a telephone call was also repeated after 2–4 weeks if the subject did not respond to the first call.
During the follow up visit, subjects completed a standardised questionnaire including questions on current smoking status, number of cigarettes smoked, motivation to stop smoking, and Fagerström Test for Nicotine Dependence (FTND).16 Those who declared complete abstention from smoking for 1 year were called sustained quitters. Self-reported non-smoking status was validated by an exhaled carbon monoxide (CO) level of less than 10 ppm (Micro CO, Micro Medical Ltd, Rochester, UK).
Statistical analyses were performed using Statistica version 6.0 software (StatSoft Inc, Tulsa, Oklahoma, USA). Tests were considered significant when p<0.05. Data distribution was analysed using the Kologomorov-Smirnov test with Lilliefors correction. Quantitative data were described using mean (SD) values. Between group characteristics were described using analysis of variance. Homogeneity of variance was assessed using Levene’s test. If a variable demonstrated normal distribution and homogeneous variance, the F ANOVA test was applied. Otherwise, a non-parametric Kruskal-Wallis H test was used. To characterise the strength of the relationships between continuous variables, Pearson correlations were used. Categorised qualitative between group analyses were performed using a Pearson χ2 test with appropriate corrections for N. To assess the influence of confounding categorised and continuous variables on smoking cessation rate after 1 year, a logistic regression model was used. Odds ratios (OR), confidence intervals (CI) and p values were calculated.
A total of 3077 subjects, representing 68.5% of those invited, attended a follow up visit: 1867 men and 1210 women. At the baseline examination one third (n = 1026) had airway obstruction which was mild in 271 (8.8%), moderate in 545 (17.7%), and severe in 210 (6.8%). There were no statistically significant differences in the smoking history, age, or sex of those who attended the follow up visit and those who did not (non-responders). However, smokers with airway obstruction were more likely to attend a follow up visit (87.2%) than smokers with normal spirometric parameters (61.6%, p<0.001). The follow up response rate also differed slightly according to the severity of airway obstruction: 80.4% with mild obstruction, 89.9% with moderate obstruction, and 89.7% with severe obstruction (p = 0.025).
The mean (SD) age of the 3077 subjects was 52.1 (10.5) years and the mean (SD) smoking exposure was 30.0 (17.0) pack-years. The mean FTND score was 4.76 (2.4) points. Descriptive statistics categorised according to spirometric results and sex are shown in table 1.
Successful smoking cessation during the 1 year follow up visit was confirmed by a low exhaled CO level in 686 subjects. Mean (SD) exhaled CO in sustained quitters was 5.01 (3.4) ppm compared with 17.2 (7.7) ppm in subjects continuing to smoke (p<0.001). Subjects who continued to smoke reported a lower mean number of cigarettes smoked per day: 19.5 (8.2) at baseline and 16.5 (8.1) at 1 year follow up. The cessation rates were 23.3% for men and 20.8% for women (p = 0.11). Smokers with airway obstruction were more likely to have quit smoking (26.6%) than those with normal spirometry (20.1%, p<0.001).
The smoking cessation rate was recalculated using the conservative assumption that all subjects who did not come for the follow up visit were continuing smokers. The overall recalculated smoking cessation rate was 13.4% (14.6% in men and 11.7% in women), and this difference was statistically significant (p = 0.01). The smoking cessation rate in those with airway obstruction remained higher than in subjects with normal spirometric parameters (16.3% v 12.0%, p = 0.0003).
Independent predictors of successful smoking cessation included older age, older age at onset of smoking, fewer cigarettes per day, lower cumulative tobacco exposure, a lower FTND score, and lower spirometric values (table 2). Subjects with moderate and severe airway obstruction were more likely to quit (table 3).
Although airway obstruction was a strong predictor of success in stopping smoking, other confounding variables could play a role. To assess possible relationships, a logistic regression analysis was used, adjusting the model for sex, age, number of cigarettes smoked daily, nicotine dependence (FTND), and airway obstruction (table 4). The logistic regression model showed significant effects of nicotine dependence, number of cigarettes smoked daily, and airflow obstruction as predictors of smoking cessation. The effect of impaired lung function was the strongest predictor of sustained cessation (OR 1.6).
Spirometric testing combined with simple short smoking cessation behavioural support resulted in a 12% sustained (12 month) smoking cessation rate in smokers with normal spirometric parameters and a 16.3% rate in smokers with airway obstruction. These rates exceed the 4–6% cessation rates reported after physician advice.17–19 In Poland in 2005, a smoking cessation initiative called “The Great Polish Smoke-out” covered around 10 million smokers. After the action, 100 000 smokers (1%) declared that they had quit smoking, another 600 000 (6%) tried to stop smoking temporarily, and 1 400 000 (14%) reduced the number of cigarettes smoked daily. These unpublished data reflect the spontaneous cessation rates after repeated smoking cessation appeals in the mass media, on billboard and pickets.
Better sustained cessation rates were reported in smokers with diseases related to or aggravated by smoking. In a large controlled British Thoracic Society (BTS) study in 1550 subjects, at the end of 1 year 9.7% had successfully stopped smoking. Smoking cessation was verified by carboxyhaemoglobin and thiocyanate measurements.20 In our study the smoking cessation rate in men was higher than in women (14.6% v 11.7%). The difference between the sexes was much lower than that observed in the BTS study where sustained smoking cessation rate in men more than doubled the cessation rate in women (12.2% v 5.3%).21
We used spirometric results to demonstrate the harmful effects of smoking and to reinforce smoking cessation advice. A similar type of intervention was applied in another study where CO levels in the exhaled air were used to show smokers how much of the lethal gas they had accumulated in their bodies. Two hundred and ten smokers were randomly allocated to four groups: control (no intervention) group, smoking cessation advice group, smoking cessation advice + CO measurements in the exhaled air group, and smoking cessation advice + offer of further help group. After 1 year the highest smoking cessation rate (17%) was observed in the exhaled CO group, compared with 15% in the smoking cessation advice group, 13% in the smoking cessation advice + further help group, and 11% in the control group.22
Smoking cessation intervention combined with spirometry was applied in the first Lung Health Study in a large cohort of subjects with mild to moderate airway obstruction.8 Behavioural techniques and nicotine replacement therapy during the first 6 months for the intensive intervention group resulted in a biochemically verified smoking cessation rate of 22% during 5 years of follow up. The 1 year cessation rate in this group was 35%. In comparison, the 5 year sustained cessation rate was only 5% in the usual care group in the First Lung Health Study; 93% of those who had quit for 5 years remained non-smokers after a total of 11 years of follow up.23
Other studies of the benefits of combining smoking cessation advice with spirometry have reported much lower cessation rates. A letter with advice to stop smoking sent to workers with workplace exposure to asbestos and low lung function resulted in a smoking cessation rate of 5.6% at 1 year which was significantly different from the 3.5% cessation rate in those who did not receive the letter.24
In another study, smoking cessation advice combined with spirometry resulted in a smoking cessation rate of 6.5% which was not significantly different from the 4.5% sustained (12 months) and validated (cotinine in urine) cessation rate in smokers who received only smoking cessation counselling or only minimal smoking cessation intervention.25 Badgett and Tanaka26 and a new report from the Agency for Healthcare Research and Quality27 have expressed doubts that spirometry substantially enhances smoking cessation rates when added to traditional techniques such as physician advice, nicotine replacement therapy, or counselling. However, a consensus statement from the United States National Lung Health Education Program (NLHEP) recommended spirometric testing to increase the motivation of smokers to quit.28 Our results help to confirm this. We believe that the results of objective spirometric measurements superimposed on a simplified diagram of FEV1 decline in non-smokers versus COPD patients was taken very seriously by the middle aged smokers attending our Program. This may explain the higher smoking cessation rate in our study compared with general practitioner’s advice.17–19
In contrast to our findings, the Lung Health Study found that smokers with moderate airway obstruction were not more likely than those with borderline to mild airway obstruction to quit smoking.29 This difference may be because the Lung Health Study excluded smokers with normal lung function, so their power to show a difference was much lower than in our study, which included over 2000 smokers with normal spirometric values.
Our smoking cessation rates would probably have been even higher if we had been able to offer nicotine replacement therapy30,31 or bupropion29,32,33 for several months at no cost to our study participants.
Molyneux et al30 compared the effects of nicotine replacement therapy, brief counselling, and minimal intervention in 274 smokers. Interventions were performed during hospitalisation. At 12 months, the smoking cessation rate was significantly higher in the group receiving nicotine replacement therapy plus brief counselling than in the group given brief counselling alone (17% v 6%). Short term positive effects of nicotine replacement therapy plus counselling—but not at 6 or 12 months—were recently reported by Hand et al.34
Smoking cessation in patients with COPD is of paramount importance. Despite continuation of airway inflammation in COPD ex-smokers,35 the mean annual decline in FEV1 returns to that observed in healthy non-smokers.23 There is also a definitive reduction in the death rate from lung cancer, myocardial infarction, and stroke in sustained non-smokers compared with continuing smokers.36,37
The number of previous cessation attempts (approximately two) characterising the population in our study was rather low. The mean number of cessation attempts in sustained ex-smokers in Poland is seven.38 Our Program probably attracted smokers who had not previously been encouraged by their general practitioners to quit.
Our study has limitations. The subjects were all volunteers from Poland and thus may not be representative of all smokers in other countries. They also showed an interest in their own health by presenting themselves to the Program, and thus were probably more motivated to quit than other smokers. Our follow up rate was 68%, but our primary findings were unchanged when we conservatively assumed that all non-responders were continuing smokers. The very limited data available on the “background quit rate” in Poland (The Great Polish Smoke-out) showed that it was very low. Since we did not randomise the study participants to spirometry versus no spirometry, unmeasured confounders may have caused the association of abnormal spirometric values with better smoking cessation rates. A large randomised clinical trial is needed to answer this important question more conclusively.
In summary, we have shown that spirometry combined with short smoking cessation advice from a physician resulted in relatively high smoking cessation rates in adult smokers. Smokers with airflow limitation had significantly higher smoking cessation rate than smokers with normal spirometry. Screening of adult smokers to detect airway obstruction using spirometric tests performed by trained technologists, combined with strong smoking cessation advice, has the potential to reduce the burden of COPD in entire countries.
The authors thank Katarzyna Szamotulska of the Institute of Mother and Child in Warsaw for help with statistical analysis.
Published Online First 29 June 2006
Supported by Polish State Committee for Scientific Research grant no. 6 PO5D 029 21.
Competing interests: none declared.
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