BACKGROUND: Greece has one of the highest rates of smoking and chronic obstructive pulmonary disease (COPD) in Europe. AIM: The study aimed to record both the disease characteristics among a sample of Greek COPD patients and the nationwide rates of newly diagnosed COPD cases. METHODS: In this noninterventional, epidemiological cross-sectional study, a representative nationwide sample of 45 respiratory centers provided data on the following: 1) the demographic and clinical characteristics of COPD patients and 2) newly diagnosed COPD cases monitored over a period of 6 months by each physician. RESULTS: Data from 6,125 COPD patients were collected. Advanced age (median age: 68 years), male predominance (71.3%), largely overweight status with median body mass index (BMI) =27.5 kg/m(2), high percentage of current and ex-smokers (89.8%), and presence of comorbidities (81.9%) were evident in the sample. According to the Global Initiative for Chronic Obstructive Lung Disease (GOLD) 2011 criteria, majority of the COPD patients had moderate or severe airflow limitation (61%). Severity of airflow limitation was significantly associated with older age, male sex, obesity, ex-smoking status, and presence of comorbidity (all P-values <0.001). A total of 61.3% of the patients received medication, mostly bronchodilators (64.4%) and fixed-dose combinations of long-acting β2-agonists and inhaled corticosteroids (39.9%), while 35.9% reported taking medication on demand. The majority (81.1%) of patients reported a preference for fewer inhalations of their bronchodilator therapy. Based on the mixed-effect Poisson model, the rate of newly diagnosed COPD cases was estimated to be 18.2% (95% confidence interval: 14.9-22.3) per pulmonologist/3 months. Of those newly diagnosed, the majority of patients had mild or moderate airflow limitation (78.2%). CONCLUSION: The Greek Obstructive Lung Disease Epidemiology and health ecoNomics study reflected the real-life profile of COPD patients and provided evidence on the profile of new COPD cases in Greece. Various demographic factors were delineated, which can assist in designing more effective diagnostic and management strategies for COPD in Greece.
BACKGROUND: Greece has one of the highest rates of smoking and chronic obstructive pulmonary disease (COPD) in Europe. AIM: The study aimed to record both the disease characteristics among a sample of Greek COPDpatients and the nationwide rates of newly diagnosed COPD cases. METHODS: In this noninterventional, epidemiological cross-sectional study, a representative nationwide sample of 45 respiratory centers provided data on the following: 1) the demographic and clinical characteristics of COPDpatients and 2) newly diagnosed COPD cases monitored over a period of 6 months by each physician. RESULTS: Data from 6,125 COPDpatients were collected. Advanced age (median age: 68 years), male predominance (71.3%), largely overweight status with median body mass index (BMI) =27.5 kg/m(2), high percentage of current and ex-smokers (89.8%), and presence of comorbidities (81.9%) were evident in the sample. According to the Global Initiative for Chronic Obstructive Lung Disease (GOLD) 2011 criteria, majority of the COPDpatients had moderate or severe airflow limitation (61%). Severity of airflow limitation was significantly associated with older age, male sex, obesity, ex-smoking status, and presence of comorbidity (all P-values <0.001). A total of 61.3% of the patients received medication, mostly bronchodilators (64.4%) and fixed-dose combinations of long-acting β2-agonists and inhaled corticosteroids (39.9%), while 35.9% reported taking medication on demand. The majority (81.1%) of patients reported a preference for fewer inhalations of their bronchodilator therapy. Based on the mixed-effect Poisson model, the rate of newly diagnosed COPD cases was estimated to be 18.2% (95% confidence interval: 14.9-22.3) per pulmonologist/3 months. Of those newly diagnosed, the majority of patients had mild or moderate airflow limitation (78.2%). CONCLUSION: The Greek Obstructive Lung Disease Epidemiology and health ecoNomics study reflected the real-life profile of COPDpatients and provided evidence on the profile of new COPD cases in Greece. Various demographic factors were delineated, which can assist in designing more effective diagnostic and management strategies for COPD in Greece.
Entities:
Keywords:
COPD; characteristics; epidemiology; health care management; health care system; nationwide sampling; new cases; newly diagnosed; prevalent cases
Chronic obstructive pulmonary disease (COPD) is characterized by persistent airflow limitation that is usually progressive and associated with an enhanced chronic inflammatory response in the airways and the lung to noxious particles or gases.1 According to the Global Initiative for Chronic Obstructive Lung Disease (GOLD) report of 2014, COPD is a common preventable and treatable disease in which exacerbations and comorbidities contribute to the overall severity in individual patients.1 COPD has been identified as the third leading cause of death globally,2 and in 2010, 4.8% of the population was diagnosed with COPD worldwide.3 Though alarming, these figures only partly represent the burden of the disease because a significant proportion of patients remain undiagnosed or misdiagnosed.4–6 In the US and Europe, the rate of underdiagnosis was estimated to range from 12% to 86%.7–9 The underutilization of spirometry as a diagnostic tool, the lack of awareness of physicians and patients about the clinical features of COPD (which includes breathlessness, chronic cough, and sputum production),10 and the difficulty in differential diagnosis between COPD and asthma contribute significantly to this wide range of undiagnosed and misdiagnosed COPDpatients.11–13 Additionally, comorbidities that are commonly present along with COPD further hinder the detection of the disease,9 and although COPD is a primary cause of death in some cases, it is often likely to be considered a contributing factor.14 There is increasing evidence that early diagnosis and early treatment of COPD lead to improvements in lung function and quality of life, as well as a reduced risk of exacerbations.15In Europe, prevalence rates of COPD were estimated to range between 2.1% and 26.1% depending on the country, age group, and methods used.16 In Greece, COPD prevalence was estimated to range between 3% and 18.4%.17–21 The variations observed in the prevalence rates are mainly due to the differences in the diagnostic methods (symptoms, physician reports, and spirometry), definition of COPD, age and sex distribution, and other population characteristics evaluated in each study.This study – the first in Greece to our knowledge – aimed to 1) estimate the nationwide rates of newly diagnosed COPD cases and 2) assess a plethora of characteristics of COPDpatients, including smoking habits, disease severity, compliance to treatment, and comorbidity, to raise treating physicians’ awareness on the diagnosis and effective management of COPD in Greece.
Methods
Study design
The Greek Obstructive Lung Disease Epidemiology and health ecoNomics (GOLDEN) study was a noninterventional, nationwide epidemiological cross-sectional study conducted in Greece over a 6-month period.To estimate the nationwide rate of newly diagnosed cases of COPD, both hospital-based and private respiratory medicine physicians were included in the study. Sampling was performed in three steps (details described by Papaioannou et al22–26): 1) the expected incident and prevalent COPD cases were estimated in each prefecture of Greece (52 administrative areas covering the whole country) and in total; 2) the expected incident COPD cases were estimated per pulmonologist in each prefecture; and lastly 3) on the basis of the ratios of expected COPD cases per pulmonologist per prefecture, three levels of sampling zones were created (Figure 1). Zone A: areas with very large hospitals, very high density of respiratory medicine physicians, and low ratios of expected COPD cases per physician; Zone B: areas with large respiratory medicine departments and many private practitioners; and Zone C: all other areas with mostly aging rural populations and few respiratory medicine physicians.
Figure 1
Map of Greece showing the sampling zones from which data were collected.
Notes: Zone A, areas with very large hospitals, very high density of respiratory medicine physicians, and low ratios of expected COPD cases per physician; Zone B, areas with large respiratory medicine departments and many private practitioners; Zone C, all other areas with mostly aging rural populations and few respiratory medicine physicians.
Pulmonologists from 45 respiratory medicine departments throughout Greece participated in the study. In total, 199 pulmonologists (124 private practitioners and 75 hospital doctors) provided data for this study. The total number of pulmonologists in Greece is approximately 1,800. According to this number, the sample of pulmonologists that participated in the study represents ~11% of the total pool of the specialty. Data collection was performed over a period of 6 months (October 2010–March 2011). During the 6 months of the study period, each pulmonologist was asked 1) to invite the first 30 consecutive COPDpatients visiting their clinic/office and who satisfied the inclusion and exclusion criteria to register for the study and 2) to monitor all newly diagnosed cases (cases diagnosed for the first time as having COPD during the specific study period) for a period of 24 weeks.
Patients
Patients could be recruited in the GOLDEN study if they provided their written informed consent and fulfilled the following inclusion and exclusion criteria:Inclusion criteria were as follows: patients >40 years of age, with a diagnosis of COPD, based on GOLD 2011 criteria,11 and with the ability to provide data on their medical history. Exclusion criteria consisted of patients who had participated in a similar study a month prior to their enrollment or had asthma.Ex-smokers were defined as smokers who had quit smoking for at least 12 months. Smoking history was measured by pack-years, defined as the number of cigarettes smoked per day divided by 20 and multiplied by the number of years of smoking. According to their smoking history, subjects were classified into three categories: never-smokers, ex-smokers, and current smokers. Compliance to therapy was assessed from physicians according to the monthly prescription of medication and the patients’ and/or relatives’ reporting on the regular use of the prescribed medication.Pre- and postbronchodilation spirometry measurements were performed in all study subjects according to the routine monitoring of COPDpatients in daily clinical practice. Forced expiratory volume in 1 second (FEV1), forced vital capacity (FVC), and the FEV1/FVC ratio were recorded. Post-bronchodilator values (30 minutes after the administration of 400 μg salbutamol with a spacer) were used for the evaluation of airflow severity, according to GOLD 2011 guidelines (Stage 1: mild COPD, FEV1 ≥80.0% predicted; Stage 2: moderate COPD, 50.0%≤ FEV1 <80.0% predicted; Stage 3: severe COPD, 30.0%≤ FEV1 <50.0%; Stage 4: very severe COPD, either FEV1 <30.0% or FEV1 <50.0% predicted with chronic respiratory failure).11A second data set included patients with “newly diagnosed” COPD who were first diagnosed during the study period (patients who were referred for the first time to a pulmonologist with diagnosis established through spirometry). The number of newly diagnosed patients was recorded through the retrospective completion of questionnaires that corresponded to a once-per-week evaluation of the new patients for the total study duration of 6 months. In calendar months, the data collection phase lasted from September to March. The characteristics of the newly diagnosed patients recorded in this study included sex, age, disease type (bronchitis/emphysema) and airflow limitation (according to GOLD 2011 classification), place of residence, and smoking history.The protocol was approved by the ethics committees of the participating research centers and the National Organization for Medicines. The study was designed, implemented, and reported in accordance with the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) Harmonized Tripartite Guidelines for Good Clinical Practice, with applicable local regulations (including European Directive 2001/83/EC and US Code of Federal Regulations Part 21), and in accordance with the ethical principles according to the Declaration of Helsinki.
Statistical methods and analysis
Categorical variables were presented using frequency and rate, whereas continuous variables were presented using descriptive statistics (median and interquartile range [IQR]).The rate ratios of the newly diagnosed patients were estimated using the mixed-effect Poisson model. Dependence of the rate of newly diagnosed cases with COPD on the prefectures, geographic divisions, hospitals, employment of the pulmonologist (hospital- or private-based practice), and season was also determined.The analysis of COPD diagnosis rate was based on the hypothesis that the number of new COPD cases follows a Poisson distribution. In order to model the repeated observations per pulmonologist (assumed to affect variability), a mixed-effects Poisson model was applied. The random effect was assumed to follow the gamma distribution.
Results
Demographic characteristics of prevalent COPD cases (1st data set)
Data from 6,125 patients were collected in the study. The baseline and clinical characteristics of the total sample are shown in Table 1. The median age of the study participants was 68 years (IQR: 60.0–75.0) and the male-to-female ratio was 2.5:1. The median duration of COPD was 10 years (IQR: 5.0–15.0). Never-smokers accounted for only 10.2% of the evaluated patients. A large proportion of the enrolled patients (18%) were newly diagnosed, many of whom had significant airflow limitation at the time of diagnosis. According to GOLD 2011 criteria, the majority of the patients were assessed with moderate or severe airflow limitation (35.4% and 25.6%, respectively).
Table 1
Demographic and clinical characteristics of the prevalent cases
Demographic characteristics
Total (N=6,125)a
“Old” cases*(N=4,850)
Cases (%) first diagnosed within the past yearb(N=1,064)
Male/female
4,367/1,758 (71.3/28.7)
3,490/1,360 (72/28)
720/344 (67.7/32.3)
Duration of COPD (years)
10.0 (5.0, 15.0)
10.0 (5.0, 15.0)
–
Body mass indexb
Normal (18.5–25 kg/m2)
1,574 (25.9)
1,245 (25.9)
277 (26.2)
Overweight (25–30 kg/m2)
2,715 (44.7)
2,133 (44.3)
495 (46.8)
Obese (>30 kg/m2)
1,781 (29.3)
1,436 (29.8)
286 (27.0)
Smoking status (N=5,999)
Current smokers
2,869 (47.8)
2,126 (44.6)
676 (64.8)
Ex-smokers
2,519 (42)
2,155 (45.2)
271 (26.0)
Never-smokers
611 (10.2)
488 (10.2)
96 (9.2)
Diagnosis (N=5,914)
Chronic bronchitis
2,856 (48.3)
2,260 (46.6)
596 (56.0)
Emphysema
801 (13.5)
659 (13.6)
142 (13.3)
Mixed disease
2,092 (35.4)
1,808 (37.3)
284 (26.7)
Undefined respiratory disease
165 (2.8)
123 (2.5)
42 (3.9)
GOLD 2011 classification of severity of airflow limitation (N=6,114)
1
1,181 (19.3)
755 (15.6)
398 (37.4)
2
2,167 (35.4)
1,705 (35.2)
399 (37.5)
3
1,567 (25.6)
1,302 (26.8)
198 (18.6)
4
1,199 (19.6)
1,088 (22.4)
69 (6.5)
Number of exacerbations in the past year
2.0 (0.0, 3.0)
–
–
Would prefer the inhaled bronchodilator therapy to include fewer inhalations
4,832 (81.1)
3,978 (83.2)
691 (70.3)
Compliance to therapy
Never/almost never
3,242 (54.5)
2,527 (52.4)
604 (65.1)
<3 times a month
1,276 (21.5)
1,088 (22.6)
143 (15.4)
1 time a week
666 (11.2)
570 (11.8)
70 (7.5)
>1 time a week
483 (8.1)
415 (8.6)
56 (6.0)
Almost every day
277 (4.7)
218 (4.5)
55 (5.9)
Respiratory failure-type I
1,422 (23.4)
1,213 (25.2)
142 (13.4)
Respiratory failure-type II
624 (10.3)
557 (11.6)
43 (4.1)
Use of nebulizer
1,316 (21.6)
1,188 (24.5)
73 (6.9)
Noninvasive mechanical ventilationb
201 (3.3)
156 (3.2)
27 (2.5)
Therapy with oxygen
1,048 (17.1)
976 (20.1)
52 (4.9)
Concomitant diseases
0
1,093 (18.2)
792 (16.6)
269 (25.7)
1
1,567 (26.1)
1,186 (24.8)
336 (32.1)
2
1,430 (23.8)
1,130 (23.7)
239 (22.8)
3
982 (16.4)
829 (17.4)
128 (12.2)
4+
934 (15.6)
841 (17.6)
76 (7.3)
Common comorbid conditions
Hypertension
3,379 (55.3)
2,797 (57.7)
470 (44.2)
Diabetes mellitus
1,253 (20.6)
1,034 (21.4)
177 (16.7)
Heart failure
1,185 (19.4)
1,021 (21.1)
119 (11.2)
Gastroesophageal reflux
934 (15.3)
767 (15.8)
144 (13.6)b
Notes:
Data are presented as median (interquartile ranges) for numerical variables or as number (%) for categorical variables.
Differences were not statistically significant; all others were significant (P<0.001).
“Old” refers to cases diagnosed for at least two years.
Abbreviations: COPD, chronic obstructive pulmonary disease; GOLD, Global Initiative for Chronic Obstructive Lung Disease.
Approximately 82% reported at least one concomitant disease, with the most common comorbid condition being hypertension (55.3%).Almost half of the patients recruited (54%) reported going through preventative vaccination and only 2.7% of the patients were part of rehabilitation programs. The majority of the patients (61.3%) were under maintenance treatment, mostly with bronchodilators (64.4%). A total of 61.4% reported using inhaled corticosteroids (ICSs), while fixed-dose combinations of long-acting β2-agonists + ICSs were reported as maintenance treatment by 39.9% of the patients. Approximately 55% of the patients in the study reported never forgetting to take their medication. The majority (81%) of the patients reported a preference for fewer inhalations of their bronchodilator therapy.Differences in the characteristics of newly diagnosed and previously diagnosed COPD cases are also illustrated in Table 1. Compared to cases with an earlier diagnosis of COPD, cases diagnosed within the past year included more females, less ex-smokers, were largely classified under stages 1 and 2, less frequent diagnosis of emphysema or mixed disease, and a low number of comorbidities (Table 1). Overall, the compliance to therapy was better among newly diagnosed cases, but a high percentage of patients forgot to take their medication regularly compared to the previously diagnosed patients (5.9% vs 4.5%; Table 1).Airflow limitation severity, defined by GOLD 2011 criteria, was significantly related to older age, male sex, obesity, ex-smoker status, and presence of more concomitant diseases (P<0.001) (Figure 2 and Table 2).
Figure 2
Descriptive statistics of the study participants according to airflow limitation as defined by GOLD guidelines.
Abbreviations: BMI, body mass index; GOLD, Global Initiative for Chronic Obstructive Lung Disease.
Table 2
Descriptive statistics of study participants according to severity of COPD (GOLD 2011)
Characteristics
Severity of COPD
1
2
3
4
P-value
Age (years)
63.0 (53.0, 71.0)
67.0 (59.0, 74.0)
67.0 (60.0, 75.0)
72.0 (66.0, 78.0)
<0.001
Duration of COPD (years)
5.0 (2.0, 10.0)
8.0 (4.0, 11.0)
10.0 (5.0, 15.0)
10.0 (6.0, 19.0)
<0.001
Pack-years
35.5 (20.0, 52.5)
40.0 (25.0, 61.3)
45.0 (20.0, 64.0)
60.0 (37.5, 83.6)
<0.001
FEV1 before bronchodilation (%)
80.0 (70.0, 87.0)
65.0 (58.0, 71.0)
52.0 (43.0, 67.0)
43.0 (29.0, 54.5)
<0.001
FEV1 after bronchodilation (%)
82.0 (75.0, 90.0)
68.0 (61.0, 75.0)
58.0 (47.0, 74.0)
46.0 (32.0, 59.0)
<0.001
Number of exacerbations in the past year
1.0 (0.0, 2.0)
1.0 (0.0, 2.0)
2.0 (1.0, 3.0)
2.0 (1.0, 4.0)
<0.001
Notes: Data are presented as median (interquartile ranges) for numerical variables.
Abbreviations: COPD, chronic obstructive pulmonary disease; FEV1, forced expiratory volume in 1 second; GOLD, Global Initiative for Chronic Obstructive Lung Disease.
COPD cases diagnosed during the follow up period (2nd data set)
Rate of new COPD cases
A total of 5,030 new cases of COPD were recorded by the 199 pulmonologists in a median follow-up time of 5.60 months (IQR: 5.37–5.83). The representativeness of the sample of pulmonologists per prefecture is illustrated in Table 3, while the rate of new diagnoses per prefecture is illustrated in Figure 3. The rate of newly diagnosed cases with COPD based on the mixed-effect Poisson model was 18.2 (95% confidence interval [CI]: 14.9–22.3) per pulmonologist/3 months. Characteristics of the newly diagnosed patients with COPD are presented in Table 4.
Table 3
Representativeness of COPD diagnoses per prefecture
Dependence of the rate of newly diagnosed cases with COPD on prefectures (results from mixed-effect Poisson model).
Notes: All the prefectures studied were compared against Attica, wherein higher number of cases was reported. Highlighted data represent significant results. Log RR >0 indicates higher incidence, while value <0 indicates lower incidence.
Characteristics of newly diagnosed patients with COPD in Greece
Characteristics
Male, %
Female, %
Total, %
Disease
Chronic bronchitis
50.09
57.71
52.07
Emphysema
16.55
11.94
15.35
Chronic bronchitis and emphysema
33.36
30.35
32.58
GOLD 2011 classification of severity of airflow limitation
0–1
29.53
43.63
33.21
2
46.40
41.15
45.03
3
19.34
13.52
17.82
4
4.74
1.71
3.95
Smoking status
Smokers
77.41
75.11
76.74
Ex-smokers
19.88
19.33
19.72
Never-smokers
2.71
5.56
3.54
Age (years)
≤44
1.54
1.53
1.54
45–49
4.63
7.68
5.52
50–54
10.09
13.01
10.95
55–59
18.45
23.28
19.86
60–64
22.41
25.51
23.31
65–69
21.10
17.28
19.98
70–74
12.73
7.41
11.18
75–79
6.09
2.90
5.16
≥80
2.95
1.41
2.50
Abbreviations: COPD, chronic obstructive pulmonary disease; GOLD, Global Initiative for Chronic Obstructive Lung Disease.
Geographical distribution of new COPD cases
There was a statistically significant heterogeneity among pulmonologists adjusted for geographic division; rates were found to be higher in populated geographic regions of Greece. The majority of the newly diagnosed COPDpatients resided in Athens (32.5%) and other urban cities (32.3%; urban cities defined as cities with >10,000 population).Statistically significant differences were observed in the rate of newly diagnosed cases depending on the hospital (P=0.009), setting of the pulmonologist (hospital- or private-based practice; P<0.001), season (P<0.001), and the level of the sampling zone (P=0.022) (data provided in Tables S1–S4, respectively). A statistically significant heterogeneity existed among pulmonologists when these factors were taken into consideration (P<0.001 for each factor).The multivariate analysis of the rate of new COPD diagnoses is presented in Table 5. A statistically significant difference in the incidence of newly diagnosed cases was observed among prefectures (P<0.001) taking into account the setting (hospital- or private-based pulmonologist) and the seasonal influence (Table 5). Hospital-based pulmonologists reported a lower rate of newly diagnosed COPD cases compared to private-based pulmonologists (lower by 70.4%) when the prefecture and the season were also considered (P<0.001; Table 5).
Table 5
Multivariate analysis of the rate of new diagnoses of COPD
RR
95% CI
P-value
Prefecture
<0.001
Central Greece
1
Thrace
0.973
(0.390, 2.427)
0.954
Peloponnese
1.167
(0.687, 1.984)
0.567
Crete
0.286
(0.154, 0.534)
<0.001
Macedonia
0.578
(0.362, 0.924)
0.022
Thessaly
0.307
(0.139, 0.678)
0.003
Aegean Islands
0.576
(0.212, 1.568)
0.281
Ionian Islands
5.526
(0.642, 47.569)
0.120
Epirus
0.68
(0.146, 3.174)
0.624
Hospital
No
1
Yes
0.296
(0.194, 0.450)
<0.001
Warmer months (April–September)
No
1
Yes
0.815
(0.769, 0.864)
<0.001
Notes: Results from the mixed-effects Poisson model.
The rate of new COPD diagnoses was also affected by the season, with lower reporting noted during the warmer months (lower by 18.5%) compared to colder months, when the prefecture and the setting were taken into consideration (P<0.001; Table 5). When all parameters of the multivariate model were considered, a statistically significant heterogeneity was observed among pulmonologists (P<0.001; 95% CI random effect: 1.15 [0.92–1.43]).On the basis of the assumption that pulmonologists see the more severe cases, an additional analysis was carried out considering only GOLD 2–4 stages of COPD. The calculated rate of these cases was 10.7 (95% CI: 8.7–13.2) per pulmonologist/3 months.Similar to the results observed for overall cases, statistically significant differences were observed in the incidence rate of newly diagnosed cases considering only GOLD 2–4 stages depending on the geographic divisions, setting of the pulmonologist, and season (P<0.001 for all factors).
Discussion
The GOLDEN study has recorded data that allow for the description of various characteristics of COPDpatients in Greece.According to the current study findings, COPD was more prevalent among older adults, men, and smokers, which is consistent with findings of previous studies in the Greek population.18–20 The current study is the first nationwide study reporting new findings since 2004 and consists of a significant sample size. Direct comparison of our results with past studies is also difficult to establish, owing to the fact that different age distributions, regions, populations, and time periods of assessment were evaluated in each study.The findings of the current study are also in accordance with those of the studies conducted worldwide, with high COPD prevalence observed among elderly individuals, men, and smokers.27–31 However, differences were also noted. The current study in Greece observed more cases of COPD in overweight individuals, whereas studies conducted in the US and Norway reported high prevalence among underweight or severely obese individuals.27,29 In contrast to our findings, higher prevalence rates of COPD were observed among women than men in the US,30 while in Africa, no significant effect of sex was seen on the prevalence of COPD.31Interestingly, patients diagnosed within the past year were less frequently diagnosed with emphysema or mixed disease, as well as having a high number of comorbid conditions, although less in number compared to patients diagnosed earlier. These study findings support the significance of early diagnosis and intervention among heavy smokers and males, as early diagnostic and educational strategies could enhance disease management and compliance to treatment.32Interestingly, half of the patients in the GOLDEN study were assessed as having mild or moderate airflow limitation (Stages 1 and 2), and according to the new GOLD guidelines, they would be expected to fall in groups A and B if they had either <2 exacerbations in the previous year or no hospitalizations. However, a significant percentage of these patients reported being under treatment with ICSs (which is recommended in patients with severe or very severe airflow limitation and/or hospitalizations or ≥2 exacerbations per year; groups C and D), indicating a low rate of adherence to global recommendations by the treating physicians.1 In addition, the low rates of preventive vaccination and rehabilitation highlight the significance of increasing awareness of these interventions for the effective management of COPD, as recommended by GOLD.1High rates of nonadherence to COPD treatment were also recorded in our study. The high proportion of patients forgetting to take their medication might be due to the presence of multiple comorbidities and thus they may need to take multiple treatments, related to higher age, while complex dosing schedules and perception of limited efficacy can also cause low compliance rates.33 Extra care should therefore be taken in educating COPDpatients on the significance of compliance to therapy to reduce symptoms and future risk. In agreement with previously reported data,17,34–36 the most commonly reported comorbidities in the studied population were hypertension, diabetes mellitus, heart failure, and gastroesophageal reflux. Sensitization of primary care physicians treating these conditions among the common COPD symptoms might provide a means to refer them for lung function testing and earlier COPD diagnosis.37The rate of newly diagnosed COPD cases observed was much higher than expected based on the international literature and >5 times higher than that calculated during the design of the study. Recent data from a Dutch study reported 1,713 newly diagnosed cases of COPD in a mean follow-up time of 3.4 years (standard deviation = ±3.2 years).38 A longitudinal cohort study conducted in Ontario, Canada, estimated the annual incidence rates of COPD from 1996 to 2007 to be 61,998 to 55,903.39 A prospective cohort study identified 648 cases of incident COPD after a median follow-up time of 11 years in the Netherlands.40 Compared to the incidence rates reported in the above-mentioned studies, the GOLDEN study recorded a total of 5,030 new cases of COPD in a mean follow-up time of 5.60 months. These differences in incidence rates can perhaps be attributed to differences in the definitions of COPD, health care settings, geographical divisions, characteristics of the study populations (with respect to age, sex, and smoking status), and methodology used for assessing COPD. An interesting finding is that the highest rates of newly diagnosed cases were recorded in urban areas and mostly by private pulmonologists. This might be indicative of the reduced rates of COPD diagnosis in rural areas, especially due to the lack of specialized pulmonologists to perform spirometry.Because the majority of the newly diagnosed patients had mild or moderate airflow limitation (78.2%), it is necessary to implement routine spirometric evaluations to identify the disease in its earlier stages. Detection of these patients at early stages of airflow limitation might assist in the optimization of disease management in the long term. As smoking is one of the main contributing causes of COPD,41 spirometry could be used in current and ex-smokers with or without respiratory symptoms as a diagnostic tool to evaluate the possible presence of COPD. These measures may identify patients with undiagnosed COPD, and early diagnosis can lead to adequate management of such cases.As with all observational studies, the GOLDEN study has strengths and weaknesses. The foremost strength is that this is the first study to assess newly diagnosed cases of COPD throughout Greece in a large sample size, allowing the collation of detailed information on various patient aspects. Furthermore, the use of spirometry in our study provides an additional validation of the classification of disease severity. The limitation of our study is the possibility that our results might have suffered an overestimation bias (overreporting bias) most probably due to the retrospective recording of newly diagnosed COPD cases and the high per capita consumption of cigarettes among the Greek population.
Conclusion
The GOLDEN study reflects the real-life profile of COPDpatients in Greece. The study has observed predominance of the elderly, men, smokers, overweight and obese individuals, moderate airflow limitation, and high comorbidity among COPDpatients. In addition, results revealed a high proportion of newly diagnosed cases of COPD, relatively low compliance to treatment guidelines, high rates of nonadherence to COPD treatment, and an increased preference for simpler treatment options (fewer inhalations). Substantial rates of new COPD diagnoses in Greece were also documented, indicating the need to increase awareness around the disease and its effective management. These data provide a framework that could be used by health professionals to adequately diagnose and manage COPD. However, more studies in well-defined samples with similar patient populations, using standard diagnostic tools are required to effectively integrate strategies to prevent and manage COPD in Greece.Dependence of the rate of newly diagnosed cases with COPD per hospitalNote: Results from mixed-effect Poisson model.Abbreviations: CI, confidence interval; COPD, chronic obstructive pulmonary disease; GH, General Hospital; RR, rate ratios; UGH, University General Hospital; GUH, General University Hospital.Dependence of the rate of newly diagnosed cases with COPD on the setting of the pulmonologist (hospital or private based)Note: Results from mixed-effect Poisson model.Abbreviations: CI, confidence interval; COPD, chronic obstructive pulmonary disease; RR, rate ratios.Dependence of the rate of newly diagnosed cases with COPD on seasonNote: Results from mixed-effect Poisson model.Abbreviations: CI, confidence interval; COPD, chronic obstructive pulmonary disease; RR, rate ratios.Dependence of the rate of newly diagnosed cases with COPD on the sample levelNote: Results from mixed-effect Poisson model.Abbreviations: CI, confidence interval; COPD, chronic obstructive pulmonary disease; RR, rate ratios.
Table S1
Dependence of the rate of newly diagnosed cases with COPD per hospital
RR
95% CI
P-value
Hospital
0.009
GH Ag. Dimitrios
1
GH Amalia Fleming
0.96
(0.179, 5.159)
0.962
GH Venizelio of Heraklion
0.25
(0.036, 1.751)
0.163
GH of Corfu
7.333
(1.487, 36.169)
0.014
GH of Kavala
0.403
(0.090, 1.811)
0.236
GH of Kalamata
2.4
(0.473, 12.170)
0.291
GH of Karditsa
0.16
(0.020, 1.312)
0.088
GH of Kozani Mamatseio
0.8
(0.146, 4.382)
0.797
GH of Komotini
0.824
(0.155, 4.366)
0.820
Sismanogleio
GH of Lamia
1.8
(0.325, 9.982)
0.501
GH Papanikolaou
0.188
(0.034, 1.041)
0.056
GH of Pyrgos A
0.636
(0.111, 3.656)
0.612
Papandreou
GH of Rethymnon
1.208
(0.238, 6.136)
0.819
GH of Serres
1
(0.186, 5.374)
1.000
GH Sismanogleio
0.762
(0.190, 3.046)
0.700
GH of thorax diseases
0.774
(0.217, 2.757)
0.693
Sotiria
GH of Chios Skylitseio
1.04
(0.195, 5.548)
0.963
GH of Chalkida
2.32
(0.457, 11.780)
0.310
GH of Chania Ag. Georgios
0.923
(0.172, 4.961)
0.926
GUH Evaggelismos
0.448
(0.099, 2.031)
0.298
GUH of Larisa
1.571
(0.306, 8.083)
0.589
GUH of Nikaia
1.36
(0.260, 7.105)
0.715
GUH Papageorgiou
0.455
(0.074, 2.777)
0.393
Special Hospital of Thorax
0.768
(0.178, 3.325)
0.725
Diseases of West Greece
UGH Attikon
0.56
(0.097, 3.217)
0.516
UGH of Heraklion Pepagni
0.88
(0.162, 4.770)
0.882
University Hospital of Alexandroupolis
1.875
(0.370, 9.508)
0.448
Note: Results from mixed-effect Poisson model.
Abbreviations: CI, confidence interval; COPD, chronic obstructive pulmonary disease; GH, General Hospital; RR, rate ratios; UGH, University General Hospital; GUH, General University Hospital.
Table S2
Dependence of the rate of newly diagnosed cases with COPD on the setting of the pulmonologist (hospital or private based)
Authors: Lucas M A Goossens; Christine L Baker; Brigitta U Monz; Kelly H Zou; Maureen P M H Rutten-van Mölken Journal: Int J Chron Obstruct Pulmon Dis Date: 2011-12-06
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Benjamin Campbell; Charles E Canter; Hélène Carabin; Jonathan Carapetis; Loreto Carmona; Claudia Cella; Fiona Charlson; Honglei Chen; Andrew Tai-Ann Cheng; David Chou; Sumeet S Chugh; Luc E Coffeng; Steven D Colan; Samantha Colquhoun; K Ellicott Colson; John Condon; Myles D Connor; Leslie T Cooper; Matthew Corriere; Monica Cortinovis; Karen Courville de Vaccaro; William Couser; Benjamin C Cowie; Michael H Criqui; Marita Cross; Kaustubh C Dabhadkar; Manu Dahiya; Nabila Dahodwala; James Damsere-Derry; Goodarz Danaei; Adrian Davis; Diego De Leo; Louisa Degenhardt; Robert Dellavalle; Allyne Delossantos; Julie Denenberg; Sarah Derrett; Don C Des Jarlais; Samath D Dharmaratne; Mukesh Dherani; Cesar Diaz-Torne; Helen Dolk; E Ray Dorsey; Tim Driscoll; Herbert Duber; Beth Ebel; Karen Edmond; Alexis Elbaz; Suad Eltahir Ali; Holly Erskine; Patricia J Erwin; Patricia Espindola; Stalin E Ewoigbokhan; Farshad Farzadfar; Valery Feigin; David T Felson; Alize Ferrari; Cleusa P Ferri; Eric M Fèvre; Mariel M Finucane; Seth Flaxman; Louise Flood; Kyle Foreman; Mohammad H Forouzanfar; Francis Gerry R Fowkes; Richard Franklin; Marlene Fransen; Michael K Freeman; Belinda J Gabbe; Sherine E Gabriel; Emmanuela Gakidou; Hammad A Ganatra; Bianca Garcia; Flavio Gaspari; Richard F Gillum; Gerhard Gmel; Richard Gosselin; Rebecca Grainger; Justina Groeger; Francis Guillemin; David Gunnell; Ramyani Gupta; Juanita Haagsma; Holly Hagan; Yara A Halasa; Wayne Hall; Diana Haring; Josep Maria Haro; James E Harrison; Rasmus Havmoeller; Roderick J Hay; Hideki Higashi; Catherine Hill; Bruno Hoen; Howard Hoffman; Peter J Hotez; Damian Hoy; John J Huang; Sydney E Ibeanusi; Kathryn H Jacobsen; Spencer L James; Deborah Jarvis; Rashmi Jasrasaria; Sudha Jayaraman; Nicole Johns; Jost B Jonas; Ganesan Karthikeyan; Nicholas Kassebaum; Norito Kawakami; Andre Keren; Jon-Paul Khoo; Charles H King; Lisa Marie Knowlton; Olive Kobusingye; Adofo Koranteng; Rita Krishnamurthi; Ratilal Lalloo; Laura L Laslett; Tim Lathlean; Janet L Leasher; 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Simon O'Hanlon; Casey Olives; Saad B Omer; Katrina Ortblad; Richard Osborne; Doruk Ozgediz; Andrew Page; Bishnu Pahari; Jeyaraj Durai Pandian; Andrea Panozo Rivero; Scott B Patten; Neil Pearce; Rogelio Perez Padilla; Fernando Perez-Ruiz; Norberto Perico; Konrad Pesudovs; David Phillips; Michael R Phillips; Kelsey Pierce; Sébastien Pion; Guilherme V Polanczyk; Suzanne Polinder; C Arden Pope; Svetlana Popova; Esteban Porrini; Farshad Pourmalek; Martin Prince; Rachel L Pullan; Kapa D Ramaiah; Dharani Ranganathan; Homie Razavi; Mathilda Regan; Jürgen T Rehm; David B Rein; Guiseppe Remuzzi; Kathryn Richardson; Frederick P Rivara; Thomas Roberts; Carolyn Robinson; Felipe Rodriguez De Leòn; Luca Ronfani; Robin Room; Lisa C Rosenfeld; Lesley Rushton; Ralph L Sacco; Sukanta Saha; Uchechukwu Sampson; Lidia Sanchez-Riera; Ella Sanman; David C Schwebel; James Graham Scott; Maria Segui-Gomez; Saeid Shahraz; Donald S Shepard; Hwashin Shin; Rupak Shivakoti; David Singh; Gitanjali M Singh; Jasvinder A Singh; Jessica Singleton; David A Sleet; Karen Sliwa; Emma Smith; Jennifer L Smith; Nicolas J C Stapelberg; Andrew Steer; Timothy Steiner; Wilma A Stolk; Lars Jacob Stovner; Christopher Sudfeld; Sana Syed; Giorgio Tamburlini; Mohammad Tavakkoli; Hugh R Taylor; Jennifer A Taylor; William J Taylor; Bernadette Thomas; W Murray Thomson; George D Thurston; Imad M Tleyjeh; Marcello Tonelli; Jeffrey A Towbin; Thomas Truelsen; Miltiadis K Tsilimbaris; Clotilde Ubeda; Eduardo A Undurraga; Marieke J van der Werf; Jim van Os; Monica S Vavilala; N Venketasubramanian; Mengru Wang; Wenzhi Wang; Kerrianne Watt; David J Weatherall; Martin A Weinstock; Robert Weintraub; Marc G Weisskopf; Myrna M Weissman; Richard A White; Harvey Whiteford; Steven T Wiersma; James D Wilkinson; Hywel C Williams; Sean R M Williams; Emma Witt; Frederick Wolfe; Anthony D Woolf; Sarah Wulf; Pon-Hsiu Yeh; Anita K M Zaidi; Zhi-Jie Zheng; David Zonies; Alan D Lopez; Christopher J L Murray; Mohammad A AlMazroa; Ziad A Memish Journal: Lancet Date: 2012-12-15 Impact factor: 79.321
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