Temporal Trends Of Pharmacologic Therapies For Patients With Chronic Obstructive Pulmonary Disease In Alberta, Canada.

Objectives: To describe the trends in pharmacologic treatment for patients newly diagnosed with chronic obstructive pulmonary disease (COPD) in Alberta, Canada.
Methods: We linked Alberta health databases to identify patients aged ≥35 years with incident COPD between April 2010 and March 2017. Incident cases were defined as those who did not have a hospitalization or outpatient visit with COPD in the previous 2 years. Patients were categorized into two groups: 1) incident cases at a hospital and 2) incident cases at an outpatient clinic, and both were followed until death or being censored by 31 March 2018. Utilization of COPD medication for 30 days following incident event and adherence in maintenance therapy over time were reported.
Results: The study included 33,169 patients with incident COPD (hospital: 9,089; outpatient: 24,080). In 18,666 (56.3%) patients starting medication within 30 days of the incident event (2010: 52.7%; 2016: 56.6%; p=0.002), SABA (60.5%) and LABA/ICS (41.6%) were most commonly used. ICS (without LABA) was used in 14.2% and was used as monotherapy in 4.5% of patients. The proportion of patients who initiated any ICS was similar (hospital: 56.7%; outpatient: 55.7%; p=0.194) and decreased in both settings over time (p<0.001). Drug adherence during the first year after the incident event was 54.3%, higher among hospital patients (66.5% vs 48.9%; p<0.001), and improved over time (2010: 53.4%; 2016: 57.4%; p<0.001).
Conclusion: The initiation of and adherence to pharmacologic therapy for patients with COPD is low but improves over time. While SABA and LABA/ICS are most commonly used, ICS utilization decreases over time.

Introduction

Chronic obstructive pulmonary disease (COPD) is common, preventable, and treatable. The aim of treatment is to relieve symptoms, prevent, and treat exacerbations, mitigate disease progression, enhance quality of life, and reduce mortality.1 Despite the best available therapy, COPD was one of the leading causes of life years lost in 2016 globally, and is a leading cause of mortality and morbidity in Canada.2,3 COPD is common among the elderly. The prevalence of COPD in Canada could be as high as 12%, and it is expected to increase further as the Canadian population ages.4,5

In combination with non-pharmacologic approaches (e.g., smoking cessation, physical activity, and pulmonary rehabilitation), pharmacologic therapy is an important component of an effective management plan for patients with COPD. It improves health status and reduces symptoms (e.g., dyspnea, cough, and sputum), frequency and severity of exacerbations, and hospital admissions.6

There are a number of studies evaluating initiation of drug therapy after the first COPD diagnosis. In a population-based study between 1997 and 2012 in Manitoba, Canada, Falk et al reported a significant number of patients with COPD not taking any medication during follow-up, overuse of inhaled corticosteroids (ICS)-containing regimens, and an increasing trend in the use of long-acting bronchodilator (LABD)-containing medications.7 Similarly, Ford et al reported a strong increase in the use of short-acting β-2 agonists (SABA), LABD, and ICS between 1999 and 2010 in the United States.8 In terms of guideline adherence, only 34% of patients in a study in Quebec and Ontario, Canada, were reported to have treatments that follow guideline recommendations. This percentage is on par with results of a study in Denmark where the use of and adherence to COPD medication were low.9,10

Alberta, Canada, has an integrated, publicly funded, and universally covered health care system with a single, province-wide institutional service provider (Alberta Health Services) serving a population of over four million people in a large geographical area. Prescription drugs are funded by both public and private programs. Currently, little is known about the trends in pharmacologic treatment for COPD in Alberta. Accordingly, we described the use of pharmacologic therapies for patients newly diagnosed with COPD in the province from fiscal years (FYs) 2010 to 2016 (1 April 2010 to 31 March 2017) in relation to guideline recommendations in place during the timeframe of this study.

Methods

Data Source And Study Population

We conducted a retrospective cohort study using six linked administrative health databases in Alberta: National Ambulatory Care Reporting System, Discharge Abstract Database, Practitioner Claims, Pharmaceutical Information Network, Alberta Health Care Insurance Plan (AHCIP) Registry, and Vital Statistics.11 The available data elements in Alberta’s administrative health databases have been described elsewhere.12,13

Patients aged ≥35 years with incident COPD between 1 April 2010 and 31 March 2017 (FYs 2010 to 2016) who were registrants of the AHCIP were included. A patient was considered to have COPD if they had a hospitalization or an outpatient visit with COPD as the primary diagnosis (International Classification of Diseases [ICD], 10th revision, codes J41, J42, J43, and J44). This case definition has a sensitivity of 85% and a specificity of 78.4%, and has been previously used in research.14,15 Incident cases were defined as those who did not have a hospitalization or ambulatory care visit with COPD as either the primary reason or comorbidity in the previous 2 years. Patients were categorized into two groups: 1) incident cases identified at a hospital (hospital patients); and 2) incident cases identified at an outpatient clinic (outpatient patients). The index date indicated when a patient was discharged from the hospital or outpatient clinic with incident COPD. For patients who visited an outpatient clinic with COPD and were admitted to hospital within 1 day, the hospital discharge date was selected as the index date. We further excluded patients who had at least two dispensations of tiotropium, ipratropium, aminophylline, or theophylline within 2 years prior to the index event, as well as patients who died during the index event.

Patients were followed from index date until death, moving out of the province, or being censored by 31 March 2018, representing a minimum follow-up of 12 months for all patients. Study design is presented in .

Drugs For COPD

We categorized pharmacologic therapies for patients with COPD into 10 groups, according to recommendations by the Global Initiative for Chronic Obstructive Lung Disease (GOLD): short-acting bronchodilators (SABD) ([1] short-acting β-agonists [SABA], [2] short-acting muscarinic antagonists [SAMA], and [3] combination SABA/SAMA in one device); long-acting bronchodilators (LABD) ([4] long-acting β-agonists [LABA], [5] long-acting muscarinic antagonists [LAMA], [6] combination LABA/LAMA in one device, and [7] combination LABA/inhaled corticosteroids [ICS] in one device); [8] ICS; [9] methylxanthines; and [10] phosphodiesterase-4 inhibitors (see ).1 A variety of COPD medication is available in Canada and was listed in the Alberta Drug Benefit Formulary during the study period (see ).16,17 As the GOLD guidelines are followed by many Canadian pulmonologists and there was not a significant change in drug recommendations during the study period, we used the 2006 and 2017 versions of these guidelines in this study.1,18,19 The latest Canadian Thoracic Society (CTS) position statement on pharmacotherapy for patients with COPD was only made available in December 2017; therefore, we used the previous CTS recommendations for management of COPD (2007) and the highlights for primary care (2008) as criteria for assessing Canadian guideline adherence.6,20,21

Main Outcomes

The main outcome was the annual rate of utilization of each drug group, which was defined as the proportion of newly diagnosed patients taking a drug group within 30 days of the incident event out of the total newly diagnosed patients in a year. Other outcomes were the distribution of the utilization of each drug group by sex and age (35–59, 60–69, 70–79, and ≥80 years) and by type of incident case (hospital or outpatient setting), drug adherence, and any changes in the proportion of patients taking maintenance therapy over time from the incident event. We also documented the use of antibiotics (Anatomical Therapeutic Chemical [ATC] code J) in addition to COPD medication.

Statistical Analysis

Patient characteristics were summarized using means (± standard deviation), medians (interquartile ranges), counts, and percentages, as appropriate. The Student T-test or Kruskal-Wallis and χ2 tests were used for continuous and categorical variables, respectively. Patient median household income was based on the 2010 Canada census, and residency (urban or rural) was based on the second digit of the postal code.22,23 Previously validated ICD codes were used to identify patient comorbidities and calculate Charlson comorbidity score.24 Comorbidities were considered to be present if they were recorded in any secondary field for a hospitalization or ambulatory care visit for incident COPD or in any field for hospitalizations or ambulatory care visits during the 2 years prior to the incident event.

We calculated drug utilization for incident COPD for each drug group. A drug dispensation was considered to be prescription initiated for incident COPD if it was first dispensed within 30 days of the index date. If a second dispensation was within 7 days of the first dispensation, it was considered part of the first dispensation.7 A 30-day cut-off was selected based on a practice in Alberta where patients with COPD are usually given a sample of 2 to 4 weeks of drug supply upon discharge. We conducted a sensitivity analysis where we explored drug utilization within 7 days of the index date to examine the effect of the time from incident event to drug utilization. Drug adherence was examined among patients who utilized COPD medication within 30 days of their index date and was defined as the proportion of days with drugs out of the number of eligible days each year after the index date (e.g., number of days from the index date to the end of the year or censored date, whichever came first). If the number of days with drugs was greater than the number of eligible days in that year (e.g., drug dispensation occurred close to the end of that year), then the number of excess days was carried over to the next year. In addition, we calculated drug utilization during each of the 5 years after the incident event regardless of when it was started. Univariate logistic regression was used for trends of drug utilization.

All analyses were performed using Stata version 14 (Stata Corporation, College Station, Texas) and R version 3.5.2 (R Foundation for Statistical Computing, Vienna); two-sided p-values <0.05 were considered statistically significant. This study was approved by the Health Research Ethics Board at the University of Alberta (IRB number: Pro00078657).

Results

There were 55,947 hospitalizations and 135,470 outpatient visits with COPD as the primary diagnosis for 62,079 unique patients aged ≥35 years in Alberta between FYs 2010 and 2016. After excluding 912 patients who did not register with the AHCIP, 15,527 patients who had a hospitalization or outpatient visit with COPD as either the primary reason or a comorbidity during the previous 2 years, 12,051 patients who had two or more dispensations of a COPD-specific drug during the previous 2 years, and 420 patients who died at the incident event, the final study cohort included 33,169 patients with incident COPD. Of them, 24,080 (72.6%) had their incident event at an outpatient clinic. A flowchart depicting patient selection is presented in Figure 1.

Figure 1

Patient selection flowchart.

Compared with patients visiting an outpatient clinic, those who were admitted to hospital for COPD were more likely to be female (overall: 50.5%; hospital: 51.5%; outpatient: 50.2%; p=0.041), older (mean age, overall: 66.1 years; hospital: 72; outpatient: 63.8; p<0.001) and were urban residents (overall: 73%; hospital: 78.2%; outpatient: 71%; p<0.001). The proportion of the most elderly group (≥80 years) was more than twice as high in the hospital group (33.6% vs 14.7%; p<0.001). Similarly, patients who were admitted to hospital had higher Charlson comorbidity scores (mean, overall: 1.9; hospital: 2.6; outpatient: 1.7; p<0.001). Diabetes mellitus (18.2%) and heart failure (10.5%) were the two most prevalent comorbidities and were both significantly higher in the hospital patients. The mean follow-up time was 44.1 months and was shorter for the hospital patients (40.2 months) compared with the outpatient patients (45.6 months, p<0.001) (see Table 1).

Table 1

Characteristics Of Studied Population

Variable	All Patients	Hospital Patients	Outpatient Patients	p
Patients, N	33,169	9,089	24,080
Females, n (%)	16,772 (50.6)	4,679 (51.5)	12,093 (50.2)	0.041
Age, in years, mean (SD)	66.1 (13.8)	72 (13.1)	63.8 (13.4)	<0.001
Age, in years, median (IQR)	66 (55–77)	73 (63–82)	63 (54–74)	<0.001
Age group, n (%)
35-59 years	11,652 (35.1)	1,739 (19.1)	9,913 (41.2)	<0.001
60-69 years	8,038 (24.2)	2,023 (22.3)	6,015 (25)
70-79 years	6,894 (20.8)	2,271 (25)	4,623 (19.2)
≥80 years	6,585 (19.9)	3,056 (33.6)	3,529 (14.7)
Urban residence, n (%)	24,203 (73)	7,110 (78.2)	17,093 (71)	<0.001
Household income ($, n, (%))
0-40,000	451 (1.4)	145 (1.6)	306 (1.3)	<0.001
40,000–60,000	4,905 (14.8)	1,528 (16.8)	3,377 (14)
60,000–80,000	18,076 (54.5)	4,842 (53.3)	13,234 (55)
80,000–100,000	6,119 (18.5)	1,587 (17.5)	4,532 (18.8)
>100,000	3,618 (10.9)	987 (10.9)	2,631 (10.9)
Comorbidities, n (%)
Myocardial infarction	1,538 (4.6)	692 (7.6)	846 (3.5)	<0.001
Heart failure	3,474 (10.5)	1,901 (20.9)	1,573 (6.5)	<0.001
Peripheral vascular disease	913 (2.8)	400 (4.4)	513 (2.1)	<0.001
Cerebrovascular disease	1,162 (3.5)	456 (5)	706 (2.9)	<0.001
Dementia	1,084 (3.3)	671 (7.4)	413 (1.7)	<0.001
Rheumatoid disease	596 (1.8)	223 (2.5)	373 (1.6)	<0.001
Peptic ulcer	488 (1.5)	170 (1.9)	318 (1.3)	<0.001
Liver disease	619 (1.9)	245 (2.7)	374 (1.6)	<0.001
Diabetes	6,039 (18.2)	2,331 (25.7)	3,708 (15.4)	<0.001
Hemiplegia or paraplegia	215 (0.7)	100 (1.1)	115 (0.5)	<0.001
Renal disease	1,253 (3.8)	675 (7.4)	578 (2.4)	<0.001
Cancer	1,706 (5.1)	743 (8.2)	963 (4)	<0.001
Metastatic cancer	510 (1.5)	217 (2.4)	293 (1.1)	<0.001
Charlson comorbidity score, mean (SD)	1.9 (1.7)	2.6 (2)	1.7 (1.5)	<0.001
Follow-up time, month, median (SD)	44.1 (25.7)	40.2 (25.8)	45.6 (25.4)	<0.001

Abbreviations: IQR, interquartile range; SD, standard deviation.

Drug Utilization After Incident Event

Of 33,169 patients with incident COPD, 14.5% (4,813) did not use any COPD medication during the study period; within 30 days of their index date, 43.7% did not use any COPD medication. Patients who were admitted to hospital were less likely to omit medication (36.3%) than their outpatient counterparts (46.4%, p<0.001), as were females (42.3%) compared with males (45.1%, p<0.001). Over the study period, the proportion of patients who took COPD medication within 30 days of their index date increased (2010: 52.7%; 2016: 56.6%; p=0.002) as a result of improvement among those admitted to hospital (2010: 56.8%; 2016: 67%; p<0.001).

Of 18,666 (56.3%) patients who took COPD medication within 30 days of their index date, 50.5% started two or more drugs. Use of SABD (65.5%) was more common in hospital patients (68.6%) compared with their outpatient counterparts (64.1%; p<0.001), as was use of LABD (average 59.2%; 73.9% in hospital patients vs 52.7% in outpatient patients; p<0.001). SABA (60.5%) and LABA/ICS (41.6%) were the two most common drugs. While the proportion of patients taking SABA remained unchanged (2010: 60.4%; 2016: 61.7; p=0.570), the proportion of patients taking LABA/ICS decreased over time (2010: 42.5%; 2016: 35.9%; p<0.001). ICS (without LABA) was used in 14.2% of patients and as monotherapy in 4.5% of patients. The proportion of patients who took any ICS was similar in both settings (hospital: 56.7%; outpatient: 55.7%; p=0.194) and decreased in both settings over time (p<0.001). However, hospital patients used more LABA/ICS (48.6% vs 38.5%, p<0.001) and less ICS in a single device (10% vs 19%, p<0.001) compared with their outpatient counterparts (see Figure 2 and Table 2).

Figure 2

Initiation of key drug group for COPD patients.

Table 2

Drug Utilization Within 30 Days After Incident Event For Patients With COPD In Alberta, 2010–2016

Group	All	2010	2011	2012	2013	2014	2015	2016
Patient, N	33,169	4,292	4,464	4,845	4,621	5,228	4,900	4,819
Patient without drug, n (%)	14,503 (43.7)	2,030 (47.3)	1,937 (43.4)	2,106 (43.5)	1,941 (42)	2,311 (44.2)	2,088 (42.6)	2,090 (43.4)
Hospital, n (%)	3,329 (36.6)	548 (43.3)	526 (37.8)	539 (37.2)	446 (35.5)	480 (35.2)	404 (33.9)	386 (33)
Outpatient, n (%)	11,174 (46.4)	1,482 (49)	1,411 (45.9)	1,567 (46.1)	1,495 (44.4)	1,831 (47.4)	1,684 (45.4)	1,704 (46.7)
Patient with drug, n (%)	18,666 (56.3)	2,262 (52.7)	2,527 (56.6)	2,739 (56.5)	2,680 (58)	2,917 (55.8)	2,812 (57.4)	2,729 (56.6)
Hospital, n (%)	5,760 (63.4)	719 (56.7)	865 (62.2)	909 (62.8)	811 (64.5)	884 (64.8)	789 (66.1)	783 (67)
Outpatient, n (%)	12,906 (53.6)	1,543 (51)	1,662 (54.1)	1,830 (53.9)	1,869 (55.6)	2,033 (52.6)	2,023 (54.6)	1,946 (53.3)
SABA, n (%)	11,288 (60.5)	1,366 (60.4)	1,520 (60.2)	1,674 (61.1)	1,602 (59.8)	1,750 (60)	1,692 (60.2)	1,684 (61.7)
Hospital, n (%)	3,646 (63.3)	430 (59.8)	539 (62.3)	571 (62.8)	485 (59.8)	556 (62.9)	526 (66.7)	539 (68.8)
Outpatient, n (%)	7,642 (59.2)	936 (60.7)	981 (59)	1,103 (60.3)	1,117 (59.8)	1,194 (58.7)	1,166 (57.6)	1,145 (58.8)
SAMA, n (%)	2,659 (14.3)	320 (14.1)	311 (12.3)	399 (14.6)	391 (14.6)	407 (14)	404 (14.4)	427 (15.6)
Hospital, n (%)	1,064 (18.5)	139 (19.3)	132 (15.3)	152 (16.7)	157 (19.4)	164 (18.6)	162 (20.5)	158 (20.2)
Outpatient, n (%)	1,595 (12.4)	181 (11.7)	179 (10.8)	247 (13.5)	234 (12.5)	243 (12)	242 (12)	269 (13.8)
SABA/SAMA, n (%)	243 (1.3)	26 (1.1)	39 (1.5)	39 (1.4)	31 (1.2)	26 (0.9)	38 (1.4)	44 (1.6)
Hospital, n (%)	95 (1.7)	6 (0.8)	16 (1.9)	13 (1.4)	18 (2.2)	10 (1.1)	19 (2.4)	13 (1.7)
Outpatient, n (%)	148 (1.2)	20 (1.3)	23 (1.4)	26 (1.4)	13 (0.7)	16 (0.8)	19 (0.9)	31 (1.6)
LABA, n (%)	197 (1.1)	16 (0.7)	19 (0.8)	11 (0.4)	16 (0.6)	50 (1.7)	43 (1.5)	42 (1.5)
Hospital, n (%)	80 (1.4)	9 (1.3)	7 (0.8)	5 (0.6)	8 (1)	17 (1.9)	17 (2.2)	17 (2.2)
Outpatient, n (%)	117 (0.9)	7 (0.5)	12 (0.7)	6 (0.3)	8 (0.4)	33 (1.6)	26 (1.3)	25 (1.3)
LAMA, n (%)	5,704 (30.6)	672 (29.7)	775 (30.7)	856 (31.3)	764 (28.5)	955 (32.7)	871 (31)	811 (29.7)
Hospital, n (%)	3,024 (52.5)	364 (50.6)	454 (52.5)	505 (55.6)	410 (50.6)	497 (56.2)	403 (51.1)	391 (49.9)
Outpatient, n (%)	2,680 (20.8)	308 (20)	321 (19.3)	351 (19.2)	354 (18.9)	458 (22.5)	468 (23.1)	420 (21.6)
LABA/LAMA, n (%)	135 (0.7)	0 (0)	0 (0)	0 (0)	0 (0)	9 (0.3)	46 (1.6)	80 (2.9)
Hospital, n (%)	29 (0.5)	0 (0)	0 (0)	0 (0)	0 (0)	0 (0)	4 (0.5)	25 (3.2)
Outpatient, n (%)	106 (0.8)	0 (0)	0 (0)	0 (0)	0 (0)	9 (0.4)	42 (2.1)	55 (2.8)
LABA/ICS, n (%)	7,769 (41.6)	961 (42.5)	1,113 (44)	1,195 (43.6)	1,152 (43)	1,218 (41.8)	1,150 (40.9)	980 (35.9)
Hospital, n (%)	2,801 (48.6)	357 (49.7)	427 (49.4)	474 (52.2)	404 (49.8)	432 (48.9)	375 (47.5)	332 (42.4)
Outpatient, n (%)	4,968 (38.5)	604 (39.1)	686 (41.3)	721 (39.4)	748 (40)	786 (38.7)	775 (38.3)	648 (33.3)
ICS, n (%)	3,031 (16.2)	411 (18.2)	404 (16)	473 (17.3)	423 (15.8)	465 (15.9)	413 (14.7)	442 (16.2)
Hospital, n (%)	575 (10)	87 (12.1)	89 (10.3)	97 (10.7)	72 (8.9)	88 (10)	62 (7.9)	80 (10.2)
Outpatient, n (%)	2,456 (19)	324 (21)	315 (19)	376 (20.6)	351 (18.8)	377 (18.5)	351 (17.4)	362 (18.6)
Methylxanthines, n (%)	37 (0.2)	9 (0.4)	12 (0.5)	7 (0.3)	3 (0.1)	4 (0.1)	0 (0)	2 (0.1)
Hospital, n (%)	14 (0.2)	3 (0.4)	5 (0.6)	2 (0.2)	2 (0.3)	1 (0.1)	0 (0)	1 (0.1)
Outpatient, n (%)	23 (0.2)	6 (0.4)	7 (0.4)	5 (0.3)	1 (0.1)	3 (0.2)	0 (0)	1 (0.1)
PDE4 inhibitors, n (%)	11 (0.1)	0 (0)	3 (0.1)	1 (0)	1 (0)	2 (0.1)	2 (0.1)	2 (0.1)
Hospital, n (%)	4 (0.1)	0 (0)	2 (0.2)	1 (0.1)	0 (0)	0 (0)	1 (0.1)	0 (0)
Outpatient, n (%)	7 (0.1)	0 (0)	1 (0.1)	0 (0)	1 (0.1)	2 (0.1)	1 (0.1)	2 (0.1)

Abbreviations: COPD, chronic obstructive pulmonary disease; ICS, inhaled corticosteroids; LABA, long-acting β-agonist; LABA/ICS, combination LABA/ICS in one device; LABA/LAMA, combination LABA/LAMA in one device; LAMA, long-acting muscarinic antagonist; PDE4 inhibitors, phosphodiesterase-4 inhibitors; SABA, short-acting β-agonist; SABA/SAMA, combination SABA/SAMA in one device; SAMA, short-acting muscarinic antagonist.

LAMA was more commonly used in hospital patients (52.5%) than in their outpatient counterparts (20.8%; p<0.001). Combination LABA/LAMA in a single device was first used in 2014 (0.3%) and increased 10-fold in just 3 years (see Table 2). However, 15.3% of patients were started with both LAMA and LABA, and use of this combination was higher in hospital patients (29.5%) than in outpatient patients (9%, p<0.001).

The proportion of patients who started SABD was similar between females (65.4%) and males (65.6%, p=0.742), while the proportion of patients who started LABD was lower among females (58.2% vs 60.4%, p=0.002). The most senior patients (aged ≥80 years) were less likely to start SABD (63.8% vs 65.9%, p=0.022) or any ICS (54.1% vs 56.5%, p=0.010) but more likely to start LABD (64.4% vs 58%, p<0.001) than their younger counterparts (see ).

Antibiotics were started in 56% of patients and were more frequently used in outpatient (57%) compared with hospital patients (53.1%, p<0.001). Antibiotics were used in 66.5%, 60.2%, and 63.6% of patients who started SABD, LABD, and any ICS, respectively.

Restricting the time to drug initiation to 7 days led to 55.4% of patients without any COPD medication after their incident event. Of those who started drugs, SABA (63.1%) and LABA/ICS (40.9%) remained the most common drugs (see ).

Drug Adherence Among Initiators

Among 18,666 patients who took drugs within 30 days of their incident event, drug adherence was 54.3% and was higher among hospital patients (66.5%) compared with outpatient patients (48.9%, p<0.001) during the first year after the incident event. Drug adherence increased to 73.9% and 60.3% in hospital and outpatient patients, respectively, during the second year, and remained relatively stable during the next 3 years (see Figure 3). Over the study period, drug adherence during the first year after the incident event improved (2010: 53.4%; 2016: 57.4%; p<0.001) due to better adherence in outpatient patients (2010: 47.6%; 2016: 53%; p<0.001) but remained unchanged in hospital patients (2010: 66%; 2016: 68.3%; p=0.174).

Figure 3

Drug adherence for COPD patients.

Drug Utilization Over Time From Incident Event

The proportion of patients who did not use any COPD maintenance medication increased from 23.6% in the first year to 40.3% (p<0.001) in the second year after the incident event and remained relatively unchanged thereafter. Accordingly, the proportion of patients who used SABA and SAMA decreased from 73.5% and 17.9% in the first year to 66% and 12.3% in the second year (both p<0.001), respectively (see Table 3). In contrast, the proportion of patients using LAMA increased from 40.3% to 45.7% (p<0.001) during the 5 years after the incident event, while the proportion of patients using LABA/ICS and ICS remained relatively stable over time. Among patients who used COPD medication, the proportion of patients who used three or more drug classes in a year remained unchanged during follow-up (first year: 38.9%; fifth year: 38.6%; p=0.688).

Table 3

COPD Drug Utilization Over Time After Incident Event In Alberta, 2010–2016

Group	Time From Incident Event
	Year 1	Year 2	Year 3	Year 4	Year 5
Patient, N	33,169	30,314	24,444	19,071	13,953
Patient without drug, n (%)	7,838 (23.6)	12,217 (40.3)	10,106 (41.3)	7,902 (41.4)	5,878 (42.1)
Patient with drug, n (%)	25,331 (76.4)	18,097 (59.7)	14,338 (58.7)	11,169 (58.6)	8,075 (57.9)
SABA, n (%)	18,607 (73.5)	11,952 (66)	9,625 (67.1)	7,486 (67)	5,542 (68.6)
SAMA, n (%)	4,535 (17.9)	2,231 (12.3)	1,752 (12.2)	1,383 (12.4)	1,083 (13.4)
SABA/SAMA, n (%)	526 (2.1)	325 (1.8)	287 (2)	223 (2)	196 (2.4)
LABA, n (%)	557 (2.2)	404 (2.2)	302 (2.1)	248 (2.2)	184 (2.3)
LAMA, n (%)	10,207 (40.3)	7,387 (40.8)	6,100 (42.5)	4,895 (43.8)	3,690 (45.7)
LABA/LAMA, n (%)	526 (2.1)	579 (3.2)	492 (3.4)	406 (3.6)	353 (4.4)
LABA/ICS, n (%)	14,997 (59.2)	10,576 (58.4)	8,549 (59.6)	6,611 (59.2)	4,810 (59.6)
ICS, n (%)	7,324 (28.9)	5,069 (28)	3,887 (27.1)	3,085 (27.6)	2,180 (27)
Methylxanthines, n (%)	98 (0.4)	80 (0.4)	78 (0.5)	56 (0.5)	45 (0.6)
PDE4 inhibitors, n (%)	72 (0.3)	83 (0.5)	55 (0.4)	56 (0.5)	44 (0.5)

Abbreviations: COPD, chronic obstructive pulmonary disease; ICS, inhaled corticosteroids; LABA, long-acting β-agonist; LABA/ICS, combination LABA/ICS in one device; LABA/LAMA, combination LABA/LAMA in one device; LAMA, long-acting muscarinic antagonist; PDE4 inhibitors, phosphodiesterase-4 inhibitors; SABA, short-acting β-agonist; SABA/SAMA, combination SABA/SAMA in one device; SAMA, short-acting muscarinic antagonist.

Discussion

Our population-based study of 33,169 patients with incident COPD between 2010 and 2016 shows that a significant portion of patients did not start medication after diagnosis. Overall, 14.5% of patients did not use any COPD medication during the study period, and 43.7% did not start medication within 30 days of the first diagnosis. However, the proportion of patients taking medication increased over time. SABA and LABA/ICS were the two most commonly used drugs. While use of SABA after the incident event remained stable over time, the use of LABA/ICS and any ICS decreased over time. While hospital patients were prescribed more LABA/ICS in combination, outpatient patients were initiated more ICS in a single device. Approximately one-fifth of patients were given ICS without LABA or as a monotherapy. The proportion of patients taking maintenance medication dropped significantly from 76.4% in the first year to 59.7% in the second year after incident event and remained relatively stable during the following years. Drug adherence was low during the first year after the incident event (54.3%) but improved over time. Hospital patients had better adherence than outpatient patients.

Our finding of poor drug utilization is consistent with previously reported results. Ingebrigtsen et al reported that only 42.2% of patients with COPD in Denmark were treated with medication during the first year after spirometry results (FEV1 <60% predicted).25 Similarly, in a retrospective study in Manitoba, Canada, Falk et al reported that 31% of patients did not use any medication after COPD diagnosis, which is double the amount of our finding.7 However, Falk et al did not report drug initiation according to time from the first diagnosis, and there was a substantial latency in drug initiation after the first diagnosis, evident by significantly higher non-initiators when the time from the index date to drug initiation was taken into consideration. Our contemporary cohort of patients with incident COPD, as well as the various efforts to improve patient medication uptake and adherence (e.g., self-management, brief counselling, community-based education and support program using case managers, and innovative technology such as wearable devices) could all be reasons for the improved drug initiation over time that we observed.26–29 We also could not exclude the effect of the introduction of more effective drugs (i.e., LAMAs are superior to SABD) and dual bronchodilation is superior to monotherapy during the study period. Nevertheless, the proportion of patients who did not use any COPD medication in the present study is still substantial enough to prompt additional research to inform factors associated with non-initiation and help design a patient education program.

The GOLD and CTS guidelines recommend initiation of SABD at early diagnosis as needed and then initiation of LABD and ICS as the severity increases, with ICS started only at a severe stage (i.e., stage III with frequent exacerbations or one or more hospital admission with COPD). However, a significant proportion of patients newly diagnosed with COPD at an outpatient clinic started ICS immediately after diagnosis, suggesting that ICS may be initiated earlier than needed. In addition, our finding that approximately 19% of patients started ICS as monotherapy or without LABA indicates poor guideline adherence for ICS initiation, as previously reported in other jurisdictions.7,9,18,20 This practice may potentially result in more harm than good to patients. While the use of ICS reduces airway inflammation and exacerbation when administered with LABD, it is also associated with an increased risk of pneumonia and other complications.30–32

Similar to Falk et al, we found that SABA was the most commonly used drug after the first diagnosis, and the proportion of patients who initiated SABD is relatively comparable between the two studies. However, we observed a much higher proportion of patients who initiated LABA/ICS, LAMA or a combination of LABA and LAMA. This trend, in combination with higher proportion of patients with LAMA or combination of LABA/LAMA in the hospital group, may reflect both availability of drugs and guideline-based treatments for more severe patients with LABD (e.g., hospital patients), especially in the context of favourable outcomes for the LABA/LAMA combination, to prevent moderate-to-severe exacerbations and improve quality of life.20,33

We found that the change in the proportion of patients taking medication occurs mainly between the first and the second year after COPD diagnosis, and patients with their incident event at an outpatient clinic were more vulnerable to non-uptake and non-adherence. This may be because of higher severity of COPD in hospital patients compared with their outpatient counterparts. It has been reported previously that the use of and adherence to maintenance medication are positively associated with the severity of COPD, and acute exacerbation is a strong predictor of medication treatment uptake.10,25 The changes in the proportion of patients taking medication and drug adherence between the first and the second year suggest that early medication uptake and adherence education interventions after the incident event might make a bigger impact, especially due to the importance of correct inhaler technique and high prevalence of critical inhaler errors among patients.34 As seen in a recent systematic review by Bryant et al, studies of several interventions have included only patients who were confirmed with COPD for more than a year or who were on theophylline for a month or more.26 Therefore, additional research is needed to draw a conclusion.

We found that more than half of the outpatient patients started antibiotics and there were more antibiotics users in outpatient than in hospital patients. The GOLD and CTS guidelines recommend antibiotics for purulent acute exacerbation (i.e., increased sputum, sputum purulence, and increased dyspnea) only.1,20,21 Therefore, higher use of antibiotics in outpatient setting may be an indication of overuse of antibiotics which was already documented in other jurisdictions. For example, a study in Spain reported frequent antibiotics use (84.5%) for patients with COPD in primary care setting.35 Another study in six European countries also found frequent antibiotics use in primary care for patients with COPD (ranged from 49% in Denmark to 93% in Russia).36 Even though the clinical benefit of antibiotics has been reported not only in COPD patients with severe exacerbation but also in patients with mild-to-moderate exacerbations,37–39 overuse of antibiotics could be associated with an increased risk of co-infections such as Clostridioides difficile colitis or increased drug resistance.40,41

Our study provides novel data on the temporal trends of maintenance medication for incident COPD, using a contemporary dataset of patients with incident COPD from heterogenous health facilities of an integrated health care system in a large and diverse geographic region with a population of over 4 million people. The findings are likely to be generalizable to other jurisdictions with similar health care system structures. However, our findings were based on drug dispensation claims, so we could not evaluate prescriptions that were not filled due to primary non-adherence. Nevertheless, we believe that the low proportion of patients not using any COPD medication (15%) should not significantly affect the overall findings. Further, we did not have information on the quality of inhaler device, nor on actual use by patients. However, while other studies used prescribing data, the claims data used in this study provide information on actual dispensation of therapy, which is a strength as these data are closer to real consumption than prescribing data. In addition, the selection of a benchmark time of 30 days after the index event is arbitrary and it may lead to a short period of time to have prescription dispensed for patients who had a full 4-week drug sample. However, adding additional 15 days to the benchmark time led to only an additional 3.7% of patients initiating drug. Therefore, it should not affect the overall findings.

Conclusion

Our population-based study of patients with COPD shows that the initiation of and adherence to maintenance therapy after the incident event is low, but is slightly improving over time. Hospital patients have better medication initiation and adherence than outpatient patients. SABA and LABA/ICS are the two most commonly initiated drugs, and ICS utilization decreases over time. In order to increase the uptake of the evidence-based therapy and improve COPD management, further education for prescribers and effective and ongoing patient education are needed.