Skip to main content
Erschienen in: BMC Pulmonary Medicine 1/2013

Open Access 01.12.2013 | Research article

Association between chronic obstructive pulmonary disease and gastroesophageal reflux disease: a national cross-sectional cohort study

verfasst von: Jinhee Kim, Jin Hwa Lee, Yuri Kim, Kyungjoo Kim, Yeon-Mok Oh, Kwang Ha Yoo, Chin Kook Rhee, Hyoung Kyu Yoon, Young Sam Kim, Yong Bum Park, Sei Won Lee, Sang Do Lee

Erschienen in: BMC Pulmonary Medicine | Ausgabe 1/2013

Abstract

Background

Gastroesophageal reflux disease (GERD) is one of the most common causes of chronic cough and a potential risk factor for exacerbation of chronic obstructive pulmonary disease (COPD). The aim of this study was to investigate the prevalence and risk factors of GERD in patients with COPD and association between GERD and COPD exacerbation.

Methods

Data were collected from the National Health Insurance Database of Korea. The subjects were 40 years old and older, who had COPD as primary or secondary diagnosis codes and utilized health care resource to receive prescriptions of COPD medication at least twice in 2009. Univariate logistic regression was performed to understand the relationship between COPD and GERD, and multiple logistic regression analysis was performed with adjustment for several confounding factors.

Results

The prevalence of GERD in COPD patients was 28% (39,987/141,057). Old age, female gender, medical aid insurance type, hospitalization, and emergency room (ER) visit were associated with GERD. Most of COPD medications except inhaled muscarinic antagonists were associated with GERD. The logistic regression analysis showed that the presence of GERD was associated with increased risk of hospitalization (OR 1.54, CI 1.50 to 1.58, p<0.001) and frequent ER visits (OR 1.55, CI 1.48 to 1.62, p<0.001).

Conclusions

The prevalence of GERD in patients with COPD was high. Old age, female gender, medical aid insurance type, and many COPD medications except inhaled muscarinic antagonists were associated with GERD. The presence of GERD was associated with COPD exacerbation.
Hinweise

Electronic supplementary material

The online version of this article (doi:10.​1186/​1471-2466-13-51) contains supplementary material, which is available to authorized users.

Competing interests

YMO has been an investigator in university-sponsored studies (Asan Institute for Life Science, University of Ulsan College of Medicine) and an industry-sponsored study (MSD Korea and AstraZeneca Korea) and has participated as a speaker at scientific meetings organized and financed by various pharmaceutical companies (Handok, GlaxoSmithKline, AstraZeneca Korea, MSD Korea, and Boehringer Ingelheim) and a magazine company (Korea Doctors’ Weekly). SDL serves as a consultant to GlaxoSmithKline and has participated as a speaker at scientific meetings organized and financed by various pharmaceutical companies (GlaxoSmithKline, AstraZeneca Korea, and Boehringer Ingelheim). The remaining authors have no conflicts of interest to disclose.

Authors’ contributions

JK participated in data analysis and drafted the manuscript. JHL conceived the study, participated in the study design and drafted the manuscript. YK and KK participated in the study design and performed data analysis. YMO, KHY, CKR, HKY, YSK, YBP, SWL, and SDL participated in the study design and were involved in revising the manuscript. All authors read and approved the final manuscript.
Abkürzungen
COPD
Chronic obstructive pulmonary disease
GERD
Gastroesophageal reflux disease
HIRA
Korean Health Insurance Review and Assessment Service
ICU
Intensive care unit
ER
Emergency room
ICS
Inhaled corticosteroid
LABAs
Long-acting beta-2 agonists
LAMAs
Long-acting muscarinic antagonists
SAMAs
Short-acting muscarinic antagonists
SABAs
Short-acting beta-2 agonists
OCS
Oral corticosteroid
LTRAs
Leukotriene receptor antagonists
OR
Odds ratio
CI
Confidence interval
PPIs
Proton pump inhibitors.

Background

Exacerbations of chronic obstructive pulmonary disease (COPD) have a significant impact on patient quality of life and can accelerate lung function decline [1], which is associated with increased morbidity and mortality [2, 3]. Gastroesophageal reflux disease (GERD) is one of the most common causes of chronic cough [4] and a potential risk factor for exacerbation of COPD [57]. GERD is a relatively common condition, affecting 10–29% of the western population [8] and 3–12% of Korean adults [9]. GER can heighten bronchial reactivity and microaspiration [1013]. Abnormal GER was objectively assessed and clearly associated to lung diseases [14, 15]. Laryngopharyngeal sensitivity is important in preventing pulmonary aspiration. Patients with cough and GERD have significantly reduced laryngopharyngeal sensitivity to air stimuli compared with healthy subjects [16]. COPD patients have flat diaphragm and increased intra-abdominal and negative intra-thoracic pressure, which could aggravate GER [17]. In addition, medications such as theophylline and inhaled beta-2 agonists may decrease the lower esophageal sphincter pressure, could facilitate GER [18, 19]. Therefore several small studies showed that GERD is more common in patients with COPD than that in those without COPD [2022]. Also it has been suggested that an increase in the frequency of COPD exacerbation can be associated with the presence of GERD [6, 7, 23, 24].
We used the National Health Insurance Database of Korea and tried to answer three questions. First question was the prevalence of GERD in patients with COPD. Second one was which factors are associated with GERD in COPD patients. Third was whether the presence of GERD is associated with exacerbation of COPD even after adjusting confounding factors.

Methods

Data source and ethical considerations

The present study used the National Health Insurance claims data for medical services provided to Koreans aged ≥ 40 years between January 1, 2009 and December 31, 2009. These data were provided by the Korean Health Insurance Review and Assessment Service (HIRA), which was established to review claims data and assess healthcare in Korea and is under the responsibility of a single agency independent from insurers, providers, and other interested parties. All Koreans are covered under the national health insurance system, and the HIRA database contains all information regarding submitted claims and prescriptions.
The HIRA claims database comprises general item, medical treatment, diagnosis, and prescription databases. The general item database contains information such as patient identifier, age, sex, and insurance type; hospital name, type, location, and medical department; and medical cost, number of days hospitalized and/or receiving outpatient, intensive care unit (ICU), and/or emergency room (ER) care. The medical treatment database contains information such as patient identifier, detailed medical treatment records, and drug administration (brand name, total days of medication, single dose, daily dose, and unit cost). The diagnosis database contains information such as patient identifier, main diagnosis, and submain diagnoses, recorded according to the International Classification of Diseases, 10th Revision (ICD-10). The prescription database contains information such as patient identifier and outpatient prescriptions. All databases were linked using a mutual identifier.
The National Evidence-Based Healthcare Collaborating Agency (NECA) ethics committee approved the present study (PIRB11-022).

Study population

The subjects of the current study were patients aged ≥40 years with COPD recorded as ICD-10 codes J42.x–J44.x (except J430) for the principal or additional diagnoses who were given prescriptions including at least one of the following medications (including oral, injected, or inhaled), at least twice per year: combinations in a single inhaler of inhaled corticosteroids (ICSs) and long-acting beta-2 agonists (LABAs), long-acting muscarinic antagonists (LAMAs), LABAs, short-acting muscarinic antagonists (SAMAs), inhalers with both short-acting beta-2 agonists (SABAs) and SAMAs, oral beta-2 agonists, or theophylline.
Patients with more than one claim per year due to cancer (C00.x–C97.x) and/or cerebrovascular disease (I60.x–I69.x) were excluded from this study because the enormous expenses claimed for treatment of these diseases were difficult to distinguish from COPD- and GERD-related medical services. Additionally, through consultation with six physicians of pulmonary medicine, we decided to exclude patients with more than one claim per year for hiatal hernia (K449), gastric surgery (K910–K913), Zollinger-Ellison syndrome (E164), systemic sclerosis (M34), achalasia (K220), pyloric obstruction (K311–K315), obesity (E66.x), alcoholic liver disease (K70.x), or ascites (K7151, R18, C786, A1830) because these diseases increase the risk for GERD.
Among subjects in the present study, 39,987 patients with COPD used medical services more than once per year for GERD (K21, K210, K219), and 101,070 patients with COPD did not have GERD.

Measures

Baseline characteristics

The variables considered to be baseline characteristics were sex, age, insurance type, hospitalization and ICU hospitalization, number of ER visits, presence of chest X-rays, spirometry, chest CT, esophagogastroduodenoscopy, 24-h esophageal pH monitoring and esophagography, COPD severity, and comorbidity. The ‘severe’ COPD group comprised patients who visited a tertiary medical institution and were prescribed ICS + LABA + LAMA, ICS + LABA + oral corticosteroid (OCS), or LAMA + OCS more than once per year, and the ‘not severe’ group comprised the remaining study subjects. ER visits were defined as cases in which an outpatient or hospitalization claim was made for emergency medical service fees or in which additional holiday/night service fees were incurred. Co-morbidities included ischemic heart disease (I20.x–I25.x, except I20.1), osteoporosis (M80.x–M82.x), depressive disorder (F32.x–F33.x), arthritis (M05.x–M09.x, M13.x), diabetes mellitus (E10.x–E14.x), congestive heart failure (I50, I50.0, I50.1, I50.9), hypertension (I10.x), anemia (D50.x–D53.x, D63.x), metabolic syndrome (E66, E78.0, E78.4, E78.5), Barrett’s esophagus (B227), gastric ulcer (K25.x), duodenal ulcer (K26.x), peptic ulcer (K27.x–K28.x), and gastroduodenitis (K29.x).

Medications used

Medications considered in the present study included ICSs, ICSs/LABAs, LAMAs, LABAs, leukotriene receptor antagonists (LTRAs), OCSs, SAMAs, SABAs, SABAs/SAMAs, oral beta-2 agonists, and theophylline covering all form of drug such as oral medications, injections, and inhalations.

Exacerbation of COPD

Exacerbation was defined as hospitalization or ER visits. Only subjects who were admitted to the department of internal medicine and received systemic corticosteroids during at least three days or recorded as ICD code for COPD exacerbation were included. Cases receiving systemic corticosteroids and inhaled short-acting bronchodilators at ER visits were included.

Statistical analyses

Data were analyzed using the SAS statistical program (ver. 9.2 [SAS Institute]); details of the analytical methods were as follows.
First, frequencies and percentages were calculated to enable comparison of baseline characteristics between COPD patients with GERD and those without GERD; the chi-squared test was used for categorical data, and the t-test was used for continuous data.
Second, the difference in medication usage between groups was determined using frequencies and percentages.
Third, univariate logistic regression was performed to understand the relationship between the general characteristics of patients with COPD and the presence of GERD, and multiple logistic regression was performed, with general characteristic variables included in the model.
Fourth, univariate logistic regression was performed to understand the relationship between the co-morbidity of patients with COPD and the presence of GERD, and the relationship between the medication usage of patients with COPD and the presence of GERD. Additionally, multiple logistic regression analysis was performed with adjustment for sex, age, type of health insurance, history of hospitalization and ICU hospitalization, category of ER visit, and COPD severity.
Fifth, univariate logistic regression was performed to understand the relationship between the presence of GERD in patients with COPD and the exacerbation of COPD, and multiple logistic regression was performed with adjustment for sex, age, type of health insurance, and COPD severity.

Results

The prevalence of GERD in patients with COPD was 28% (39,987/141,057).
General characteristics of patients with COPD according to the presence or absence of GERD were summarized in Table 1. COPD patients with GERD had more hospitalization and ER visits than those without GERD (all p < 0.001), whereas there was no difference of ICU hospitalization between two groups. More patients with COPD and GERD used medical services for treatment of all kinds of comorbidity than did those without GERD (all p < 0.001; Table 1).
Table 1
General characteristic of subjects with COPD, classified according to the presence of GERD
 
Variables
COPD with GERD
COPD without GERD
p
  
No.
(%)
No.
(%)
 
Total
39,987
(100.0)
101,070
(100.0)
 
Sex
    
<0.001
 
Male
22,967
(57.4)
61,674
(61.0)
 
 
Female
17,020
(42.6)
39,396
(39.0)
 
Age (years)
     
 
Mean ± SD
68.86 ± 10.18
69.71 ± 11.67
<0.001
 
40–49
1,904
(4.8)
5,243
(5.2)
<0.001
 
50–59
5,349
(13.4)
13,052
(12.9)
 
 
60–69
11,954
(29.9)
26,801
(26.5)
 
 
70–79
15,239
(38.1)
37,329
(36.9)
 
 
80+
5,541
(13.9)
18,645
(18.4)
 
Type of insurance
    
<0.001
 
Health insurance
32,823
(82.1)
85,755
(84.8)
 
 
Medical aid
7,164
(17.9)
15,315
(15.2)
 
Hospitalization
    
<0.001
 
Never
24,179
(60.5)
70,547
(69.8)
 
 
Ever
15,808
(39.5)
30,523
(30.2)
 
ICU hospitalization
    
0.377
 
Never
39,817
(99.6)
100,605
(99.5)
 
 
Ever
170
(0.4)
465
(0.5)
 
No. of ER visits
     
 
Mean ± SD
1.65 ± 1.24
1.50 ± 1.02
<0.001
 
0
31,260
(78.2)
84,116
(83.2)
<0.001
 
1–2
7,446
(18.6)
15,121
(15.0)
 
 
3–4
984
(2.5)
1,506
(1.5)
 
 
5+
297
(0.7)
327
(0.3)
 
Chest X-ray
    
<0.001
 
Never
22,671
(56.7)
65,494
(64.8)
 
 
Ever
17,316
(43.3)
35,576
(35.2)
 
Spirometry
    
<0.001
 
Never
23,353
(58.4)
65,891
(65.2)
 
 
Ever
16,634
(41.6)
35,179
(34.8)
 
Chest CT
    
0.055
 
Never
39,583
(99.0)
100,159
(99.1)
 
 
Ever
404
(1.0)
911
(0.9)
 
Esophagogastroduodenoscopy
    
<0.001
 
Never
27,923
(69.8)
94,638
(93.6)
 
 
Ever
12,064
(30.2)
6,432
(6.4)
 
24-h esophageal pH monitoring
    
<0.001
 
Never
39,974
(100.0)
101,067
(100.0)
 
 
Ever
13
(0.0)
3
(0.0)
 
Esophagography
    
<0.001
 
Never
39,352
(98.4)
100,566
(99.5)
 
 
Ever
635
(1.6)
504
(0.5)
 
COPD severity
    
<0.001
 
No
32,629
(81.6)
84,427
(83.5)
 
 
Yes
7,358
(18.4)
16,643
(16.5)
 
Comorbidity
     
 
Ischemic heart disease
8,262
(20.7)
15,696
(15.5)
<0.001
 
Osteoporosis
8,723
(21.8)
15,281
(15.1)
<0.001
 
Depressive disorder
4,838
(12.1)
6,442
(6.4)
<0.001
 
Arthritis
10,299
(25.8)
18,035
(17.8)
<0.001
 
Diabetes mellitus
10,426
(26.1)
22,478
(22.2)
<0.001
 
Congestive heart failure
3,819
(9.6)
8,661
(8.6)
<0.001
 
Hypertension
20,734
(51.9)
48,802
(48.3)
<0.001
 
Anemia
2,354
(5.9)
3,973
(3.9)
<0.001
 
Metabolic syndrome
9,296
(23.2)
16,428
(16.3)
<0.001
 
Barrett’s esophagus
23
(0.1)
4
(0.0)
<0.001
 
Gastric ulcer
14,308
(35.8)
17,940
(17.8)
<0.001
 
Duodenal ulcer
2,489
(6.2)
2,404
(2.4)
<0.001
 
Peptic ulcer
8,856
(22.1)
13,657
(13.5)
<0.001
 
Gastroduodenitis
36,196
(90.5)
77,151
(76.3)
<0.001
No. = number of subjects; SD = standard deviation; ICU = intensive care unit; ER = emergency room.
Medication used for both group was summarized in Table 2.
Table 2
Medication utilization of patients with COPD, classified according to the presence of GERD
 
COPD with GERD (n= 39,987)
COPD without GERD (n= 101,070)
 
No.
(%)
No.
(%)
ICS
6,439
(8.8)
12,734
(7.7)
ICS/LABA
14,436
(19.6)
33,593
(20.3)
LAMA
11,760
(16.0)
28,529
(17.2)
LABA
35
(0.0)
79
(0.0)
LTRA
11,468
(15.6)
23,158
(14.0)
OCS
24,031
(32.7)
51,421
(31.0)
SAMA
7,763
(10.6)
16,850
(10.2)
SABA
14,596
(19.9)
32,904
(19.9)
SABA/SAMA
1,048
(1.4)
2,603
(1.6)
Oral beta-2 agonists
23,530
(32.0)
55,856
(33.7)
Theophylline
33,859
(46.0)
83,688
(50.5)
No. = number of subjects; ICS = inhaled corticosteroid; LABA = long-acting beta-2 agonist; LAMA = long-acting muscarinic antagonist; LTRA = leukotriene receptor antagonist; OCS = oral corticosteroid; SAMA = short-acting muscarinic antagonist; SABA = short-acting beta-2 agonist.
A regression model including general characteristics indicated that more female than male patients with COPD had GERD and more patients in their 50s, 60s, and 70s had GERD compared with those in their 40s. More GERD was observed in the medical aid group compared with the health insurance group, and in subjects with hospitalization experience compared with subjects without hospitalization. Less GERD was observed in subjects with ICU hospitalization than in those without. More GERD were observed in subjects with ER visits compared with those without (Table 3).
Table 3
Association of GERD with general characteristics in patients with COPD
 
Unadjusted
Adjusted*
  
OR
95% CI
p
OR
95% CI
p
Sex
      
 
Male
1 (ref)
  
1 (ref)
  
 
Female
1.16
(1.13, 1.19)
<0.001
1.22
(1.19, 1.25)
<0.001
Age (years)
      
 
40–49
1 (ref)
  
1 (ref)
  
 
50–59
1.13
(1.06, 1.20)
<0.001
1.15
(1.08, 1.22)
<0.001
 
60–69
1.23
(1.16, 1.30)
<0.001
1.26
(1.19, 1.34)
<0.001
 
70–79
1.12
(1.06, 1.19)
<0.001
1.10
(1.04, 1.17)
<0.001
 
80+
0.82
(0.77, 0.87)
<0.001
0.75
(0.71, 0.80)
<0.001
Type of insurance
      
 
Health insurance
1 (ref)
  
1 (ref)
  
 
Medical aid
1.22
(1.19, 1.26)
<0.001
1.15
(1.12, 1.19)
<0.001
Hospitalization
      
 
Never
1 (ref)
  
1 (ref)
  
 
Ever
1.51
(1.48, 1.55)
<0.001
1.46
(1.42, 1.50)
<0.001
ICU hospitalization
      
 
Never
1 (ref)
  
1 (ref)
  
 
Ever
0.93
(0.78, 1.10)
0.385
0.68
(0.57, 0.82)
<0.001
Number of ER visits
      
 
0
1 (ref)
  
1 (ref)
  
 
1–2
1.33
(1.29, 1.37)
<0.001
1.11
(1.07, 1.15)
<0.001
 
3–4
1.76
(1.62, 1.91)
<0.001
1.40
(1.29, 1.53)
<0.001
 
5+
2.44
(2.09, 2.86)
<0.001
1.87
(1.59, 2.21)
<0.001
COPD severity
      
 
No
1 (ref)
  
1 (ref)
  
 
Yes
1.14
(1.11, 1.18)
<0.001
1.02
(0.99, 1.06)
0.186
OR = odds ratio; ICU = intensive care unit; ER = emergency room.
*Adjusted for sex, age, type of insurance, hospitalization, ICU hospitalization, number of ER visits by category, and COPD severity.
The ‘severe’ group comprised patients who visited a tertiary medical institution and were prescribed ICS + LABA + LAMA, ICS + LABA + oral corticosteroid (OCS), or LAMA + OCS more than once per year.
After adjusting for sex, age, type of health insurance, hospitalization, ICU hospitalization, category of ER visit, and COPD severity, more patients with COPD and GERD had comorbidities except congestive heart failure. More GERD was observed among patients using ICSs, ICSs/LABAs, LTRAs, OCSs, oral beta-2 agonists, and theophylline (all p < 0.001). However, less GERD was observed in association with SAMAs use [odds ratio (OR) 0.96, 95% confidence interval (CI) 0.93 to 0.99; Table 4].
Table 4
Association of GERD with comorbidities and medication utilization in patients with COPD
 
Unadjusted
Adjusted*
  
OR
95% CI
p
OR
95% CI
p
Comorbidity
      
 
Ischemic heart disease
1.42
(1.38, 1.46)
<0.001
1.31
(1.27, 1.35)
<0.001
 
Osteoporosis
1.57
(1.52, 1.61)
<0.001
1.46
(1.42, 1.51)
<0.001
 
Depressive disorder
2.02
(1.95, 2.10)
<0.001
1.87
(1.79, 1.94)
<0.001
 
Arthritis
1.60
(1.55, 1.64)
<0.001
1.55
(1.51, 1.60)
<0.001
 
Diabetes mellitus
1.23
(1.20, 1.27)
<0.001
1.14
(1.11, 1.17)
<0.001
 
Congestive heart failure
1.13
(1.08, 1.17)
<0.001
1.04
(0.99, 1.08)
0.078
 
Hypertension
1.15
(1.13, 1.18)
<0.001
1.11
(1.09, 1.14)
<0.001
 
Anemia
1.53
(1.45, 1.61)
<0.001
1.39
(1.32, 1.46)
<0.001
 
Metabolic syndrome
1.56
(1.52, 1.61)
<0.001
1.45
(1.41, 1.49)
<0.001
 
Barrett’s esophagus
14.46
(5.01, 41.73)
<0.001
15.10
(5.21, 43.79)
<0.001
 
Gastric ulcer
2.58
(2.52, 2.65)
<0.001
2.45
(2.38, 2.51)
<0.001
 
Duodenal ulcer
2.72
(2.57, 2.88)
<0.001
2.65
(2.51, 2.81)
<0.001
 
Peptic ulcer
1.82
(1.77, 1.88)
<0.001
1.74
(1.69, 1.79)
<0.001
 
Gastroduodenitis
2.96
(2.85, 3.07)
<0.001
2.82
(2.71, 2.92)
<0.001
Drug
      
 
ICS
1.33
(1.29, 1.38)
<0.001
1.13
(1.09, 1.17)
<0.001
 
ICS/LABA
1.14
(1.11, 1.16)
<0.001
1.05
(1.02, 1.08)
<0.001
 
LAMA
1.06
(1.03, 1.09)
<0.001
0.99
(0.96, 1.02)
0.567
 
LABA
1.12
(0.75, 1.67)
0.568
1.11
(0.74, 1.65)
0.624
 
LTRA
1.35
(1.31, 1.39)
<0.001
1.27
(1.23, 1.30)
<0.001
 
OCS
1.45
(1.42, 1.49)
<0.001
1.37
(1.34, 1.40)
<0.001
 
SAMA
1.20
(1.17, 1.24)
<0.001
0.96
(0.93, 0.99)
0.015
 
SABA
1.19
(1.16, 1.22)
<0.001
1.02
(0.99, 1.04)
0.237
 
SABA/SAMA
1.02
(0.95, 1.10)
0.627
0.97
(0.90, 1.04)
0.339
 
Oral beta-2 agonists
1.16
(1.13, 1.19)
<0.001
1.11
(1.09, 1.14)
<0.001
 
Theophylline
1.15
(1.11, 1.19)
<0.001
1.10
(1.07, 1.14)
<0.001
OR = odds ratio; ICS = inhaled corticosteroid; LABA = long-acting beta-2 agonist; LAMA = long-acting muscarinic antagonist; LTRA = leukotriene receptor antagonist; OCS = oral corticosteroid; SAMA = short-acting muscarinic antagonist; SABA = short-acting beta-2 agonist.
*Adjusted for sex, age, type of health insurance, hospitalization, ICU hospitalization, number of ER visits by category, and COPD severity.
After adjusting for sex, age, type of health insurance, and COPD severity, the regression model demonstrated that COPD exacerbation was more prevalent among patients with GERD than among those without GERD, as indicated by more hospitalization (OR 1.54, 95% CI 1.50 to 1.58) and ER visits (OR 1.55, 95% CI 1.48 to 1.62; Table 5).
Table 5
Association of GERD with exacerbation in patients with COPD
 
Hospitalization
ICU
ER visit (0–1vs. ≥2)
  
OR
95% CI
p
OR
95% CI
p
OR
95% CI
p
GERD
No
1 (ref)
  
1 (ref)
  
1 (ref)
  
Yes
1.51
(1.48, 1.55)
<0.001
0.92
(0.78, 1.10)
0.377
1.55
(1.48, 1.62)
<0.001
GERD*
No
1 (ref)
  
1 (ref)
  
1 (ref)
  
 
Yes
1.54
(1.50, 1.58)
<0.001
0.93
(0.78, 1.11)
0.441
1.55
(1.48, 1.62)
<0.001
ICU = intensive care unit; ER = emergency room; OR = odds ratio.
*Adjusted for sex, age, type of health insurance, and COPD severity.

Discussion

To the best of our knowledge, this is the first nationwide study of the largest number of COPD patients to investigate the prevalence of GERD and the association between COPD and GERD. The prevalence of GERD in patients with COPD was 28%, which is very high since the prevalence in Korean general population is around 12%. It is similar to previous ones reported in Japan [7, 24], and lower than the others, which were 32%–37% in the USA and 53.6% in Iran [6, 20, 23], even though these studies investigated only a small number of patients with COPD. Some of them showed higher prevalence in COPD patients compared with controls [7, 20]. These support that GERD is one of the most common comorbidities in patients with COPD.
In the present study, several things are different from the previous studies. One is that inhaled anticholingergics may decrease or, at least, not increase risk of GERD, whereas a previous study reported that relative risk of GERD increased with using inhaled anticholinergics [22]. In another study, the effect of medication was not statistically significant or hard to be evaluated because COPD patients are usually treated by multiple medications and have both pulmonary and other systemic problems [21]. Our hypothesis is that inhaled anticholinergics might reduce GER through suppressing cough. They have been used for chronic cough [25], which is one of the most common symptoms in COPD patients. Chronic bronchitis and GERD are the most common causes of chronic cough [26]. Ipratropium has been effective even for cough hypersensitivity induced by upper respiratory tract infection [27]. Tiotropium inhibits cough reflex sensitivity to capsaicin in subjects with acute viral upper respiratory tract infection [28]. The antitussive effect of tiotropium may occur through a mechanism other than bronchodilation. Additionally, tiotropium reduced lung inflammation in a mouse model of chronic GER [29]. Even though ICSs have been known to be effective for chronic cough, especially asthma [26], our subjects exclusively had COPD. The prevalence of GER was reported to increase according to use of ICS in COPD patients [22], which is consistent with our result. Combined inhalers of ICS and LABA have been popular in Korea, whereas use of LABA alone was very limited because representative LABAs such as salmeterol or formoterol were no longer imported or produced. The reason was that salmeterol as a single agent without ICS seemed to increase respiratory mortality in patients with asthma [30], which made physicians hesitate to prescribe LABA without ICS even for COPD. Therefore it is inadequate to evaluate their effects on GERD. When a patient takes variable drugs at the same time, as well as COPD medication, drug interaction will happen.
Another different thing is that ICU admission due to COPD exacerbation was not associated with GERD. It may be possible for COPD patients with GERD to complain more cough or heartburn and feel exacerbation earlier than do those without GERD, which make them more frequently have unscheduled visit or ER visit, leading to hospitalization to general ward but not to ICU. The other possibility is that patients with COPD to be admitted to ICU do not have chance to be examined whether they have GERD or they are too dyspneic to present any symptoms of GERD. Despite of higher proportion of comorbidities in patients with COPD and GERD, the rate of ICU admission was lower than those in those without GERD, even though total hospitalization rate was higher. There would be the third possibility. In this study, prescriptions of proton pump inhibitors (PPIs) were given for COPD patients with GERD more frequently than those without GERD (data are not shown). PPIs decrease frequency of GERD symptoms such as cough [31], which would rather prevent COPD patients from progression to ICU admission. One small prospective study demonstrated that PPIs reduced the number of exacerbation in COPD patients without GERD [32].
In this study, the logistic regression analysis, even after adjusting several factors such as age, gender, type of health insurance, and COPD severity, showed that the presence of GERD was independently associated with COPD exacerbation such as hospitalization or frequent ER visits. Since lung function data were not available in the present study, definition of severe COPD was based upon medication information and health care resource utilization. Although the degree of airflow limitation has been used as one of the most important criteria of COPD severity, it does not always reflect dyspnea, exercise capacity, quality of life, or exacerbation frequency [33]. Recently updated Global initiative for chronic Obstructive Lung Disease (GOLD) emphasizes combined assessment of COPD, which includes symptoms and risk of exacerbations as well as degree of airflow limitation [3]. To supplement our weakness, patients with severe COPD were defined as those who satisfied both of the followings. One is that they used a tertiary health care resource, which means respiratory specialist’s care, and the other is that they received medications for maximum effect such as triple therapy (ICS + LABA + LAMA) or OCS-containing long-acting bronchodilator, which may mean medication for exacerbations. These are possible under nationwide health insurance system of Korea, which divide health care resources into primary, secondary and tertiary and recommend people to use those step by step. Previous studies observed very small number of patients and simply compared frequency of exacerbation in COPD patients with GERD with in those without GERD [6, 7, 23, 24]. They did not fully consider clinically important confounding factors such as age, gender, and COPD severity. Moreover, in two reports of them, COPD patients with GERD showed lower lung function as well as higher frequency of exacerbation than did those without GERD [23, 24]. Therefore it might be hard to conclude whether frequent exacerbation was related to the presence of GERD or severe airflow limitation. Our study is also limited by its retrospective and cross-sectional design, and thus we cannot definitely conclude that GERD causes exacerbations of COPD. However, in a recent prospective study, patients with COPD and GERD had more exacerbation and hospitalization than in those without GERD, with crude relative risks of 3.42 and 3.66, respectively [24]. Since they excluded patients taking drugs for acid suppression, their relative risks may be higher than odds ratio in this study reflecting real world.
There are several limitations of this study. GERD was defined only by diagnosis codes even though about one third of GERD patients performed diagnostic tests related to GERD. In Korea, diseases of upper gastrointestinal (UGI) tract are more common than those in western countries and the incidence of stomach cancer has been the highest among all types of cancer. Therefore, as a health screening program of the Korean National Health Insurance System, all people can receive one of EGD or UGI series every two years from the age of 40 years. Nevertheless there might be a selection bias since symptomatic patients are likely to receive a diagnostic test. Definition of COPD was based on both of diagnosis codes and prescription data, which were exclusively determined by physicians. Although 37% of our subjects performed spirometry, this figure includes both general physicians and specialists. To exclude asthma patients, we excluded those receiving only LTRA or only ICS or only SABA. Nevertheless, there was still a possibility that some of our subjects may have asthma. As considering this, we additionally analyzed each data from only male or from subjects with prescription including LAMA, which is specific for COPD (Additional file 1: Table S1 and Table S2). Both analyses showed the same trend as Table 5. Since we used health insurance claim data, relatively important clinical data such as smoking history, lung function, and body mass index cannot be quantified although we tried to exclude patients with asthma or those with obesity or other diseases increasing risk of GERD by using both diagnosis codes and prescription data. Relatively not severe exacerbation such as unscheduled clinic visits or medication change were not included. Also, our definition of exacerbation might exclude some patients receiving only antibiotics without systemic corticosteroid. However, despite of these limitations, the present study clearly exhibits various interactive relationships between COPD and GERD. Although it would be hard to conclude complex relationship between COPD and GERD considering own severity and specific medications for both diseases and their interactions, we need to pay more attention to unraveling the heterogeneous causes of exacerbations.

Conclusions

GERD is one of the most common comorbidities and a factor associated with exacerbation in patients with COPD. COPD-related medications except inhaled anticholinergics are associated with increased risk of GERD.

Acknowledgements

This study was supported by a grant from the Korea Healthcare Technology R&D Project (A102065).
Open Access This article is published under license to BioMed Central Ltd. This is an Open Access article is distributed under the terms of the Creative Commons Attribution License ( https://​creativecommons.​org/​licenses/​by/​2.​0 ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Competing interests

YMO has been an investigator in university-sponsored studies (Asan Institute for Life Science, University of Ulsan College of Medicine) and an industry-sponsored study (MSD Korea and AstraZeneca Korea) and has participated as a speaker at scientific meetings organized and financed by various pharmaceutical companies (Handok, GlaxoSmithKline, AstraZeneca Korea, MSD Korea, and Boehringer Ingelheim) and a magazine company (Korea Doctors’ Weekly). SDL serves as a consultant to GlaxoSmithKline and has participated as a speaker at scientific meetings organized and financed by various pharmaceutical companies (GlaxoSmithKline, AstraZeneca Korea, and Boehringer Ingelheim). The remaining authors have no conflicts of interest to disclose.

Authors’ contributions

JK participated in data analysis and drafted the manuscript. JHL conceived the study, participated in the study design and drafted the manuscript. YK and KK participated in the study design and performed data analysis. YMO, KHY, CKR, HKY, YSK, YBP, SWL, and SDL participated in the study design and were involved in revising the manuscript. All authors read and approved the final manuscript.
Literatur
1.
Zurück zum Zitat Donaldson GC, Seemungal TA, Bhowmik A, Wedzicha JA: Relationship between exacerbation frequency and lung function decline in chronic obstructive pulmonary disease. Thorax. 2002, 57 (10): 847-852. 10.1136/thorax.57.10.847.CrossRefPubMedPubMedCentral Donaldson GC, Seemungal TA, Bhowmik A, Wedzicha JA: Relationship between exacerbation frequency and lung function decline in chronic obstructive pulmonary disease. Thorax. 2002, 57 (10): 847-852. 10.1136/thorax.57.10.847.CrossRefPubMedPubMedCentral
2.
Zurück zum Zitat Soler-Cataluña JJ, Martínez-García MA, Román Sánchez P, Salcedo E, Navarro M, Ochando R: Severe acute exacerbations and mortality in patients with chronic obstructive pulmonary disease. Thorax. 2005, 60 (11): 925-931. 10.1136/thx.2005.040527.CrossRefPubMedPubMedCentral Soler-Cataluña JJ, Martínez-García MA, Román Sánchez P, Salcedo E, Navarro M, Ochando R: Severe acute exacerbations and mortality in patients with chronic obstructive pulmonary disease. Thorax. 2005, 60 (11): 925-931. 10.1136/thx.2005.040527.CrossRefPubMedPubMedCentral
4.
Zurück zum Zitat Pratter MR: Overview of common causes of chronic cough: ACCP evidence-based clinical practice guidelines. Chest. 2006, 129 (Suppl): 59-62.CrossRef Pratter MR: Overview of common causes of chronic cough: ACCP evidence-based clinical practice guidelines. Chest. 2006, 129 (Suppl): 59-62.CrossRef
5.
Zurück zum Zitat Hurst JR, Vestbo J, Anzueto A, Locantore N, Müllerova H, Tal-Singer R, Miller B, Lomas DA, Agusti A, Macnee W, Calverley P, Rennard S, Wouters EF, Wedzicha JA, Evaluation of COPD Longitudinally to Identify Predictive Surrogate Endpoints (ECLIPSE) Investigators: Susceptibility to exacerbation in chronic obstructive pulmonary disease. N Engl J Med. 2010, 363 (12): 1128-1138. 10.1056/NEJMoa0909883.CrossRefPubMed Hurst JR, Vestbo J, Anzueto A, Locantore N, Müllerova H, Tal-Singer R, Miller B, Lomas DA, Agusti A, Macnee W, Calverley P, Rennard S, Wouters EF, Wedzicha JA, Evaluation of COPD Longitudinally to Identify Predictive Surrogate Endpoints (ECLIPSE) Investigators: Susceptibility to exacerbation in chronic obstructive pulmonary disease. N Engl J Med. 2010, 363 (12): 1128-1138. 10.1056/NEJMoa0909883.CrossRefPubMed
6.
Zurück zum Zitat Rascon-Aguilar IE, Pamer M, Wludyka P, Cury J, Coultas D, Lambiase LR, Nahman NS, Vega KJ: Role of gastroesophageal reflux symptoms in exacerbations of COPD. Chest. 2006, 130 (4): 1096-1101. 10.1378/chest.130.4.1096.CrossRefPubMed Rascon-Aguilar IE, Pamer M, Wludyka P, Cury J, Coultas D, Lambiase LR, Nahman NS, Vega KJ: Role of gastroesophageal reflux symptoms in exacerbations of COPD. Chest. 2006, 130 (4): 1096-1101. 10.1378/chest.130.4.1096.CrossRefPubMed
7.
Zurück zum Zitat Terada K, Muro S, Sato S, Ohara T, Haruna A, Marumo S, Kinose D, Ogawa E, Hoshino Y, Niimi A, Terada T, Mishima M: Impact of gastro-oesophageal reflux disease symptoms on COPD exacerbation. Thorax. 2008, 63 (11): 951-955. 10.1136/thx.2007.092858.CrossRefPubMed Terada K, Muro S, Sato S, Ohara T, Haruna A, Marumo S, Kinose D, Ogawa E, Hoshino Y, Niimi A, Terada T, Mishima M: Impact of gastro-oesophageal reflux disease symptoms on COPD exacerbation. Thorax. 2008, 63 (11): 951-955. 10.1136/thx.2007.092858.CrossRefPubMed
8.
Zurück zum Zitat Dent J, El-Serag HB, Wallander MA, Johansson S: Epidemiology of gastro-oesophageal reflux disease: a systemic review. Gut. 2005, 54 (5): 710-717. 10.1136/gut.2004.051821.CrossRefPubMedPubMedCentral Dent J, El-Serag HB, Wallander MA, Johansson S: Epidemiology of gastro-oesophageal reflux disease: a systemic review. Gut. 2005, 54 (5): 710-717. 10.1136/gut.2004.051821.CrossRefPubMedPubMedCentral
9.
Zurück zum Zitat Jung HK: Epidemiology of gastresophageal reflux disease in Asia: a systematic review. J Neurogastroenterol Motil. 2011, 17 (1): 14-27. 10.5056/jnm.2011.17.1.14.CrossRefPubMedPubMedCentral Jung HK: Epidemiology of gastresophageal reflux disease in Asia: a systematic review. J Neurogastroenterol Motil. 2011, 17 (1): 14-27. 10.5056/jnm.2011.17.1.14.CrossRefPubMedPubMedCentral
10.
Zurück zum Zitat Field SK, Evans JA, Price LM: The effects of acid perfusion of the esophagus on ventilation and respiratory sensation. Am J Respir Crit Care Med. 1998, 157 (4): 1058-1062. 10.1164/ajrccm.157.4.9707094.CrossRefPubMed Field SK, Evans JA, Price LM: The effects of acid perfusion of the esophagus on ventilation and respiratory sensation. Am J Respir Crit Care Med. 1998, 157 (4): 1058-1062. 10.1164/ajrccm.157.4.9707094.CrossRefPubMed
11.
Zurück zum Zitat Cuttitta G, Cibella F, Visconti A, Scichilone N, Bellia V, Bonsignore G: Spontaneous gastresophageal reflux and airway patency during the night in adult asthmatics. Am J Respir Crit Care Med. 2000, 161 (1): 177-181. 10.1164/ajrccm.161.1.9808014.CrossRefPubMed Cuttitta G, Cibella F, Visconti A, Scichilone N, Bellia V, Bonsignore G: Spontaneous gastresophageal reflux and airway patency during the night in adult asthmatics. Am J Respir Crit Care Med. 2000, 161 (1): 177-181. 10.1164/ajrccm.161.1.9808014.CrossRefPubMed
12.
Zurück zum Zitat Alexander JA, Hunt LW, Patel AM: Prevalence, pathophysiology, and treatment of patients with asthma and gastresophageal reflux disease. Mayo Clin Proc. 2000, 75 (10): 1055-1063. 10.4065/75.10.1055.CrossRefPubMed Alexander JA, Hunt LW, Patel AM: Prevalence, pathophysiology, and treatment of patients with asthma and gastresophageal reflux disease. Mayo Clin Proc. 2000, 75 (10): 1055-1063. 10.4065/75.10.1055.CrossRefPubMed
13.
Zurück zum Zitat Phua SY, McGarvey LP, Ngu MC, Ing AJ: Patients with gastro-oesophageal reflux disease and cough have impaired laryngopharyngeal mechanosensitivity. Thorax. 2005, 60 (6): 488-491. 10.1136/thx.2004.033894.CrossRefPubMedPubMedCentral Phua SY, McGarvey LP, Ngu MC, Ing AJ: Patients with gastro-oesophageal reflux disease and cough have impaired laryngopharyngeal mechanosensitivity. Thorax. 2005, 60 (6): 488-491. 10.1136/thx.2004.033894.CrossRefPubMedPubMedCentral
14.
Zurück zum Zitat Sontag SJ, O’Connell S, Khandelwal S, Miller T, Nemchausky B, Schnell TG, Serlovsky R: Most asthmatics have gastroesophageal reflux with or without bronchodilator therapy. Gastroenterology. 1990, 99 (3): 613-620.CrossRefPubMed Sontag SJ, O’Connell S, Khandelwal S, Miller T, Nemchausky B, Schnell TG, Serlovsky R: Most asthmatics have gastroesophageal reflux with or without bronchodilator therapy. Gastroenterology. 1990, 99 (3): 613-620.CrossRefPubMed
15.
Zurück zum Zitat Savarino E, Bazzica M, Zentilin P, Pohl D, Parodi A, Cittadini G, Negrini S, Indiveri F, Tutuian R, Savarino V, Ghio M: Gastroesophageal reflux and pulmonary fibrosis in scleroderma: a study using pH-impedance monitoring. Am J Respir Crit Care Med. 2009, 179 (5): 408-413. 10.1164/rccm.200808-1359OC.CrossRefPubMed Savarino E, Bazzica M, Zentilin P, Pohl D, Parodi A, Cittadini G, Negrini S, Indiveri F, Tutuian R, Savarino V, Ghio M: Gastroesophageal reflux and pulmonary fibrosis in scleroderma: a study using pH-impedance monitoring. Am J Respir Crit Care Med. 2009, 179 (5): 408-413. 10.1164/rccm.200808-1359OC.CrossRefPubMed
16.
Zurück zum Zitat Sweet MP, Patti MG, Hoopes C, Hays SR, Golden JA: Gastro-oesophageal reflux and aspiration in patients with advanced lung disease. Thorax. 2009, 64 (2): 167-173. 10.1136/thx.2007.082719.CrossRefPubMed Sweet MP, Patti MG, Hoopes C, Hays SR, Golden JA: Gastro-oesophageal reflux and aspiration in patients with advanced lung disease. Thorax. 2009, 64 (2): 167-173. 10.1136/thx.2007.082719.CrossRefPubMed
17.
Zurück zum Zitat Pauwels A, Blondeau K, Dupont LJ, Sifrim D: Mechanisms of increased gastroesophageal reflux in patients with cystic fibrosis. Am J Gastroenterol. 2012, 107 (9): 1346-1353. 10.1038/ajg.2012.213.CrossRefPubMed Pauwels A, Blondeau K, Dupont LJ, Sifrim D: Mechanisms of increased gastroesophageal reflux in patients with cystic fibrosis. Am J Gastroenterol. 2012, 107 (9): 1346-1353. 10.1038/ajg.2012.213.CrossRefPubMed
18.
Zurück zum Zitat Stein MR, Towner TG, Weber RW, Mansfield LE, Jacobson KW, McDonnell JT, Nelson HS: The effect of theophylline on the lower esophageal sphincter pressure. Ann Allergy. 1980, 45 (4): 238-241.PubMed Stein MR, Towner TG, Weber RW, Mansfield LE, Jacobson KW, McDonnell JT, Nelson HS: The effect of theophylline on the lower esophageal sphincter pressure. Ann Allergy. 1980, 45 (4): 238-241.PubMed
19.
Zurück zum Zitat Crowell MD, Zayat EN, Lacy BE, Schettler-Duncan A, Liu MC: The effects of an inhaled beta(2)-adrenergic agonist on lower esophageal function: a dose–response study. Chest. 2001, 120 (4): 1184-1189. 10.1378/chest.120.4.1184.CrossRefPubMed Crowell MD, Zayat EN, Lacy BE, Schettler-Duncan A, Liu MC: The effects of an inhaled beta(2)-adrenergic agonist on lower esophageal function: a dose–response study. Chest. 2001, 120 (4): 1184-1189. 10.1378/chest.120.4.1184.CrossRefPubMed
20.
Zurück zum Zitat Mokhlesi B, Morris AL, Huang CF, Curcio AJ, Barrett TA, Kamp DW: Increased prevalence of gastresophageal reflux symptoms in patients with COPD. Chest. 2001, 119 (4): 1043-1048. 10.1378/chest.119.4.1043.CrossRefPubMed Mokhlesi B, Morris AL, Huang CF, Curcio AJ, Barrett TA, Kamp DW: Increased prevalence of gastresophageal reflux symptoms in patients with COPD. Chest. 2001, 119 (4): 1043-1048. 10.1378/chest.119.4.1043.CrossRefPubMed
21.
Zurück zum Zitat Casanova C, Baudet JS, del Valle VM, Martin JM, Aguirre-Jaime A, de Torres JP, Celli BR: Increased gastro-oesophageal reflux disease in patients with severe COPD. Eur Respir J. 2004, 23 (6): 841-845. 10.1183/09031936.04.00107004.CrossRefPubMed Casanova C, Baudet JS, del Valle VM, Martin JM, Aguirre-Jaime A, de Torres JP, Celli BR: Increased gastro-oesophageal reflux disease in patients with severe COPD. Eur Respir J. 2004, 23 (6): 841-845. 10.1183/09031936.04.00107004.CrossRefPubMed
22.
Zurück zum Zitat García Rodríguez LA, Ruigómez A, Martín-Merino E, Johansson S, Wallander MA: Relationship between gastresophageal reflux disease and COPD in UK primary care. Chest. 2008, 134 (6): 1223-1230. 10.1378/chest.08-0902.CrossRefPubMed García Rodríguez LA, Ruigómez A, Martín-Merino E, Johansson S, Wallander MA: Relationship between gastresophageal reflux disease and COPD in UK primary care. Chest. 2008, 134 (6): 1223-1230. 10.1378/chest.08-0902.CrossRefPubMed
23.
Zurück zum Zitat Rogha M, Behravesh B, Pourmoghaddas Z: Association of gastresophageal reflux disease symptoms with exacerbations of chronic obstructive pulmonary disease. J Gastrointestin Liver Dis. 2010, 19 (3): 253-256.PubMed Rogha M, Behravesh B, Pourmoghaddas Z: Association of gastresophageal reflux disease symptoms with exacerbations of chronic obstructive pulmonary disease. J Gastrointestin Liver Dis. 2010, 19 (3): 253-256.PubMed
24.
Zurück zum Zitat Takada K, Matsumoto S, Kojima E, Iwata S, Okachi S, Ninomiya K, Morioka H, Tanaka K, Enomoto Y: Prospective evaluation of the relationship between acute exacerbations of COPD and gastroesophageal reflux disease diagnosed by questionnaire. Respir Med. 2011, 105 (10): 1531-1536. 10.1016/j.rmed.2011.03.009.CrossRefPubMed Takada K, Matsumoto S, Kojima E, Iwata S, Okachi S, Ninomiya K, Morioka H, Tanaka K, Enomoto Y: Prospective evaluation of the relationship between acute exacerbations of COPD and gastroesophageal reflux disease diagnosed by questionnaire. Respir Med. 2011, 105 (10): 1531-1536. 10.1016/j.rmed.2011.03.009.CrossRefPubMed
25.
Zurück zum Zitat Braman SS: Chronic cough due to chronic bronchitis: ACCP evidence-based clinical practice guidelines. Chest. 2006, 129 (1 Suppl): 104-115.CrossRef Braman SS: Chronic cough due to chronic bronchitis: ACCP evidence-based clinical practice guidelines. Chest. 2006, 129 (1 Suppl): 104-115.CrossRef
26.
Zurück zum Zitat Molassiotis A, Bryan G, Caress A, Bailey C, Smith J: Pharmacological and non-pharmacological interventions for cough in adults with respiratory and non-respiratory diseases: a systematic review of the literature. Respir Med. 2010, 104 (7): 934-944. 10.1016/j.rmed.2010.02.010.CrossRefPubMed Molassiotis A, Bryan G, Caress A, Bailey C, Smith J: Pharmacological and non-pharmacological interventions for cough in adults with respiratory and non-respiratory diseases: a systematic review of the literature. Respir Med. 2010, 104 (7): 934-944. 10.1016/j.rmed.2010.02.010.CrossRefPubMed
27.
Zurück zum Zitat Lowry R, Wood A, Higenbottam T: The effect of anticholinergic bronchodilator therapy on cough during upper respiratory tract infections. Br J Clin Pharmacol. 1994, 37 (2): 187-191. 10.1111/j.1365-2125.1994.tb04259.x.CrossRefPubMedPubMedCentral Lowry R, Wood A, Higenbottam T: The effect of anticholinergic bronchodilator therapy on cough during upper respiratory tract infections. Br J Clin Pharmacol. 1994, 37 (2): 187-191. 10.1111/j.1365-2125.1994.tb04259.x.CrossRefPubMedPubMedCentral
28.
Zurück zum Zitat Dicpinigaitis PV, Spinner L, Santhyadka G, Negassa A: Effect of tiotropium on cough reflex sensitivity in acute viral cough. Lung. 2008, 186 (6): 369-374. 10.1007/s00408-008-9114-6.CrossRefPubMed Dicpinigaitis PV, Spinner L, Santhyadka G, Negassa A: Effect of tiotropium on cough reflex sensitivity in acute viral cough. Lung. 2008, 186 (6): 369-374. 10.1007/s00408-008-9114-6.CrossRefPubMed
29.
Zurück zum Zitat Cui Y, Devillier P, Kuang X, Wang H, Zhu L, Xu Z, Xia Z, Zemoura L, Advenier C, Chen H: Tiotropium reduction of lung inflammation in a model of chronic gastro-oesophageal reflux. Eur Respir J. 2010, 35 (6): 1370-1376. 10.1183/09031936.00139909.CrossRefPubMed Cui Y, Devillier P, Kuang X, Wang H, Zhu L, Xu Z, Xia Z, Zemoura L, Advenier C, Chen H: Tiotropium reduction of lung inflammation in a model of chronic gastro-oesophageal reflux. Eur Respir J. 2010, 35 (6): 1370-1376. 10.1183/09031936.00139909.CrossRefPubMed
30.
Zurück zum Zitat Nelson HS, Weiss ST, Bleecker ER, Yancey SW, Dorinsky PM, SMART Study Group: The Salmeterol Multicenter Asthma Research Trial: a comparison of usual pharmacotherapy for asthma or usual pharmacotherapy plus salmeterol. Chest. 2006, 129 (1): 15-26. 10.1378/chest.129.1.15.CrossRefPubMed Nelson HS, Weiss ST, Bleecker ER, Yancey SW, Dorinsky PM, SMART Study Group: The Salmeterol Multicenter Asthma Research Trial: a comparison of usual pharmacotherapy for asthma or usual pharmacotherapy plus salmeterol. Chest. 2006, 129 (1): 15-26. 10.1378/chest.129.1.15.CrossRefPubMed
31.
Zurück zum Zitat Poe RH, Kallay MC: Chronic cough and gastresophageal reflux disease: experience with specific therapy for diagnosis and treatment. Chest. 2003, 123 (3): 679-684. 10.1378/chest.123.3.679.CrossRefPubMed Poe RH, Kallay MC: Chronic cough and gastresophageal reflux disease: experience with specific therapy for diagnosis and treatment. Chest. 2003, 123 (3): 679-684. 10.1378/chest.123.3.679.CrossRefPubMed
32.
Zurück zum Zitat Sasaki T, Nakayama K, Yasuda H, Yoshida M, Asamura T, Ohrui T, Arai H, Araya J, Kuwano K, Yamaya M: A randomized, single-blind study of lansoprazole for the prevention of exacerbations of chronic obstructive pulmonary disease in older patients. J Am Geriatr Soc. 2009, 57 (8): 1453-1457. 10.1111/j.1532-5415.2009.02349.x.CrossRefPubMed Sasaki T, Nakayama K, Yasuda H, Yoshida M, Asamura T, Ohrui T, Arai H, Araya J, Kuwano K, Yamaya M: A randomized, single-blind study of lansoprazole for the prevention of exacerbations of chronic obstructive pulmonary disease in older patients. J Am Geriatr Soc. 2009, 57 (8): 1453-1457. 10.1111/j.1532-5415.2009.02349.x.CrossRefPubMed
33.
Zurück zum Zitat Agusti A, Calverley PM, Celli B, Coxson HO, Edwards LD, Lomas DA, MacNee W, Miller BE, Rennard S, Silverman EK, Tal-Singer R, Wouters E, Yates JC, Vestbo J, Evaluation of COPD Longitudinally to Identify Predictive Surrogate Endpoints (ECLIPSE) investigators: Characterisation of COPD heterogeneity in the ECLIPSE cohort. Respir Res. 2010, 11: 122-PubMedPubMedCentral Agusti A, Calverley PM, Celli B, Coxson HO, Edwards LD, Lomas DA, MacNee W, Miller BE, Rennard S, Silverman EK, Tal-Singer R, Wouters E, Yates JC, Vestbo J, Evaluation of COPD Longitudinally to Identify Predictive Surrogate Endpoints (ECLIPSE) investigators: Characterisation of COPD heterogeneity in the ECLIPSE cohort. Respir Res. 2010, 11: 122-PubMedPubMedCentral
Metadaten
Titel
Association between chronic obstructive pulmonary disease and gastroesophageal reflux disease: a national cross-sectional cohort study
verfasst von
Jinhee Kim
Jin Hwa Lee
Yuri Kim
Kyungjoo Kim
Yeon-Mok Oh
Kwang Ha Yoo
Chin Kook Rhee
Hyoung Kyu Yoon
Young Sam Kim
Yong Bum Park
Sei Won Lee
Sang Do Lee
Publikationsdatum
01.12.2013
Verlag
BioMed Central
Erschienen in
BMC Pulmonary Medicine / Ausgabe 1/2013
Elektronische ISSN: 1471-2466
DOI
https://doi.org/10.1186/1471-2466-13-51

Weitere Artikel der Ausgabe 1/2013

BMC Pulmonary Medicine 1/2013 Zur Ausgabe

Leitlinien kompakt für die Innere Medizin

Mit medbee Pocketcards sicher entscheiden.

Seit 2022 gehört die medbee GmbH zum Springer Medizin Verlag

Reizdarmsyndrom: Diäten wirksamer als Medikamente

29.04.2024 Reizdarmsyndrom Nachrichten

Bei Reizdarmsyndrom scheinen Diäten, wie etwa die FODMAP-arme oder die kohlenhydratreduzierte Ernährung, effektiver als eine medikamentöse Therapie zu sein. Das hat eine Studie aus Schweden ergeben, die die drei Therapieoptionen im direkten Vergleich analysierte.

Notfall-TEP der Hüfte ist auch bei 90-Jährigen machbar

26.04.2024 Hüft-TEP Nachrichten

Ob bei einer Notfalloperation nach Schenkelhalsfraktur eine Hemiarthroplastik oder eine totale Endoprothese (TEP) eingebaut wird, sollte nicht allein vom Alter der Patientinnen und Patienten abhängen. Auch über 90-Jährige können von der TEP profitieren.

Niedriger diastolischer Blutdruck erhöht Risiko für schwere kardiovaskuläre Komplikationen

25.04.2024 Hypotonie Nachrichten

Wenn unter einer medikamentösen Hochdrucktherapie der diastolische Blutdruck in den Keller geht, steigt das Risiko für schwere kardiovaskuläre Ereignisse: Darauf deutet eine Sekundäranalyse der SPRINT-Studie hin.

Bei schweren Reaktionen auf Insektenstiche empfiehlt sich eine spezifische Immuntherapie

Insektenstiche sind bei Erwachsenen die häufigsten Auslöser einer Anaphylaxie. Einen wirksamen Schutz vor schweren anaphylaktischen Reaktionen bietet die allergenspezifische Immuntherapie. Jedoch kommt sie noch viel zu selten zum Einsatz.

Update Innere Medizin

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.