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Comorbidity in patients with chronic obstructive pulmonary disease in family practice: a cross sectional study

Abstract

Background

Chronic obstructive pulmonary disease (COPD) is frequent and often coexists with other diseases. The aim of this study was to quantify the prevalence of COPD and related chronic comorbidity among patients aged over 40 years visiting family practices in an area of Madrid.

Methods

An observational, descriptive, cross-sectional study was conducted in a health area of the Madrid Autonomous Region (Comunidad Autónoma de Madrid). The practice population totalled 198,670 persons attended by 129 Family Physicians (FPs), and the study population was made up of persons over the age of 40 years drawn from this practice population. Patients were deemed to have COPD if this diagnosis appeared on their clinical histories. Prevalence of COPD; prevalence of a further 25 chronic diseases in patients with COPD; and standardised prevalence ratios, were calculated.

Results

Prevalence of COPD in family medicine was 3.2% (95% CI 3.0–3.3) overall, 5.3% among men and 1.4% among women; 90% of patients presented with comorbidity, with a mean of 4 ± 2.04 chronic diseases per patient, with the most prevalent related diseases being arterial hypertension (52%), disorders of lipid metabolism (34%), obesity (25%), diabetes (20%) and arrhythmia (15%). After controlling for age and sex, the observed prevalence of the following ten chronic diseases was higher than expected: heart failure; chronic liver disease; asthma; generalised artherosclerosis; osteoporosis; ischaemic heart disease; thyroid disease; anxiety/depression; arrhythmia; and obesity.

Conclusions

Patients with COPD, who are frequent in family practice, have a complex profile and pose a clinical and organisational challenge to FPs.

Peer Review reports

Background

Chronic obstructive pulmonary disease (COPD) is frequent, incapacitating at advanced stages, leads to the death of the patient and, by 2030, is expected to be the fourth leading cause of death and the seventh leading cause of loss of disability adjusted life years (DALYs) [1].

Until the year 2000, few epidemiological studies had addressed COPD, and those that were undertaken mostly targeted the population aged over 40 years. A meta-analysis of studies published up to 2004 estimated COPD prevalence among over 40-year-olds to be 10% [2]; however, heterogeneity in the definition of case makes difficult results comparison. Latest estimations in Spain, using the GOLD criteria, set COPD prevalence in 10.2%, with strong variation among different regions and an important fall regarding a previous study performed ten years earlier [3].

Comorbidity is present in one third of the adult population and its prevalence increases with age, eventually affecting 60% of the population aged 55 to 74 years [4]; moreover, it has been observed that certain chronic diseases tend to be present in clusters [5].

COPD often coexists with other diseases, and this related comorbidity is a key prognostic factor of the consequences of COPD. Some of these diseases occur regardless of COPD, some are related by virtue of having a common cause(s), and others share risk factors [6]. For instance, inflammation brought about by smoking can be a common route for a series of diseases, such as ischaemic heart disease, heart failure, osteoporosis, anaemia, cancer, depression and diabetes [7]. COPD associated comorbidity contributes to symptoms, determines the quality of life [8, 9], increments healthcare costs [10] and increments the mortality of patients suffering it [11].

Clinical research targets isolated diseases. Chronic care is geared to managing individual diseases (disease management programmes), and the clinical practice guidelines that underpin these models likewise focus on isolated diseases [12]. Stratification of COPD patients takes into account the level of obstruction, but does not consider the burden of comorbidity, notwithstanding its implications.

Research into comorbidity is scant, and relatively new: there are population studies, hospital studies and primary healthcare studies. Most of these studies have analyzed the association between COPD and several isolated diseases; and a few of them have analyzed its association to larger groups of chronic diseases; however the strong differences between diseases from the two groups make their comparison difficult. COPD is a disease suffered by elder people and several associated diseases are frequent for their high prevalence among elder population; as a consequence a key point when studying comorbidity is to distinguish clearly if these diseases are independent or if they are associated more frequently than in general population [13].

The aim of this study was to quantify the prevalence of COPD, and quantify and describe diagnosed COPD-related chronic comorbidity in family practices in an area of Madrid, using EMR-based data.

Methods

We conducted an observational, descriptive, cross-sectional study in a health area of the Madrid Autonomous Region (Comunidad de Madrid), based on a catchment population of 887,134 and data pertaining to 2007.

The study used the EMRs of 198,670 persons, corresponding to the practice population allocated to 129 FPs who, by way of inclusion criteria, met the following two EMR utilization quality requirements: 1) annotations in over 64% of medical visits (75th percentile); and 2) a mean of more than four care episodes per patient.

Data were drawn from clinical histories. The following data were extracted from each patient: age; sex; and all diagnoses, grouped into Expanded Diagnosis Clusters (EDC), for which medical advice had been sought in 2007.

Patients were classified by means of the ACG® Case–Mix System, version 7, developed by Johns Hopkins University [14] on the premise that the level of resources needed for health care is related to disease burden. This system enables mutually exclusive groups of patients, Adjusted Clinical Groups (ACGs), to be formed on the basis of the criterion of similar use of resources, using age, sex and morbidity across a given period of time (usually one year) for the purpose. In addition, patients can be regrouped, according to their respective ACGs, into six Resource Utilisation Bands (RUBs), which are based on expected use and range from zero (RUB 0) to very high expected use (RUB 5). Furthermore, the system also generates categories, known as Expanded Diagnosis Clusters (EDCs), which group patients by reference to clinical criteria. The ACG ® Case – Mix System has been widely used and has proved its validity to study morbidity and comorbidity [1518].

Using pre-established criteria [19], the research team made an initial selection of 40 chronic EDCs and, in a second stage, identified 26 so-called: “high prevalence–high impact” (HP/HI) [16] EDCs, which met one or both of the following criteria: 1) prevalence above the 50th percentile; and/or 2) over 50% of patients included in RUBs 4 and 5 (elevated use of resources). We included COPD in this list of 26 EDCs, and analysed its association with the other 25 high prevalence - high impact chronic EDCs.

As a first step and using health records patients older than 40 and suffering EDC RES04 were selected. EDC RES04 includes emphysema, chronic bronchitis and COPD. Using this criterion for case definition, the prevalence of COPD seen in family practices was then calculated with its 95% confidence level (95% CI).

All statistical analyses were performed using the SPSS statistical package, version 15.0. In the case of qualitative variables, frequency distributions were calculated, along with their 95% CIs where pertinent; in the case of quantitative variables, means and their standard deviations were calculated, normality was tested, and parametric or non-parametric tests were applied, depending on the distribution of the variable.

Presence of comorbidity was analysed, by quantifying the proportion of patients included in each of the designated 6 comorbidity levels, ranging from isolated COPD to COPD associated with 5 or more comorbidities. The association between COPD and each of the 25 HP/HI diseases studied was quantified, and standardised prevalence ratios (observed/expected prevalence) were calculated, assuming independence between the diseases analysed and COPD. For the calculation of expected frequencies, age and sex were adjusted for using the indirect method.

The study was approved by the Ethics Committee of the Puerta de Hierro University Teaching Hospital.

Results

The 129 FPs covered by the study attended a total practice population of 198,670 patients, made up of 104,003 women (52.35%) and 94,667 men (47.65%). Of the 3,183 patients diagnosed with COPD, 3,124 (98%) were aged 40 years or over, comprising 2,376 (76%) men and 748 (24%) women. Patients’ mean age was 71.41 ± 11.50 years, without significant differences between the sexes. COPD prevalence in the family practices targeted was 3.2% (95% CI 3.0 – 3.3), and was higher in men than in women (5.3% vs. 1.4%), a difference of 3.9%, p < 0.01.

COPD patients are a population with an elevated comorbidity. They have a mean of 4 ± 2.04 chronic HP/HI diseases. The number of diseases was higher in women than in men (Mann–Whitney U-test, p < 0.01) and rose with age (Table 1). Only 9% of patients had isolated COPD, and over half had three or more chronic problems in addition to COPD (Table 2). Table 3 shows the percentage distribution of the 25 chronic diseases studied among COPD patients, overall and by sex: 52% of patients presented with arterial hypertension, 34% with lipid metabolism disorders, 25% with obesity, 20% with diabetes, 15% with arrhythmia and 14% with thyroid disease. Men had more ischaemic heart disease, generalised artherosclerosis, diabetes mellitus, chronic liver disease, malignant neoplasms and chronic renal failure (p < 0.01). Women suffered more from asthma, arterial hypertension, osteoporosis, thyroid disease, degenerative joint disease and anxiety/depression (p < 0.01).

Table 1 Chronic diseases / Patient
Table 2 Comorbidity levels in patients with COPD
Table 3 Prevalence of chronic diseases in patients with COPD

To control for the effect of age, Table 4 shows observed and expected prevalences adjusted for age and sex. In COPD patients, ten of the 25 diseases studied were more frequent than would have been expected, and the following were particularly noteworthy, with congestive heart failure being 2.4 times, chronic liver disease 89%, asthma 73%, generalised artherosclerosis 67%, osteoporosis 42% and ischaemic heart disease 41% more frequent. The remaining fifteen studied diseases present no meaningful differences in prevalence with respect to those found in general population even though some of them are very frequent among patients suffering COPD.

Table 4 Standardised prevalence of chronic diseases in patients with COPD

Discussion

COPD is a disease that affects 3.2% of the population attended by FPs; 90% of patients had one or more related diseases and 55% presented with three or more additional chronic diseases.

The morbidity seen in primary health care comes close to that reported in population-based studies. In a health care system such as Spain’s, citizens are not only required to register with a FP, but, in order to be eligible for hospital care, must first consult their FP.

In recently published population-based epidemiological study conducted in Spain, COPD prevalence was estimated at 10.2%. It is well known that COPD tends to be underdiagnosed by FPs [2022]. In our case a prevalence of 3.2% falls in the range found by Halbert [2] in the studies that used respiratory symptoms based medical diagnosis as case definition. Comparing to the prevalence data from the previously referenced study [3] which used GOLD criteria as case definition, family doctors might have been underdiagnosing 69% of the patient’s population suffering COPD. This is a high underdiagnosis ratio, comparable with that of previous studies, and it has scarcely changed in the last ten years.

At the date of our study, all health centres were supplied with spirometers but FPs are widely known to make little use of this particular diagnostic technique [2325]. Furthermore, underdiagnosis may also be influenced by FPs’ attitude to this disease: indeed, reluctance to label the patient is such that treatment may even be initiated before the formal diagnosis has been entered on the clinical record [26].

Of the total, only 9% of patients presented with COPD alone, and the remainder tended to have a mean of four of the 25 chronic diseases studied. Being an aged population, the diseases or conditions involved are not only specific to older persons, but are also present at a frequency that is higher than expected, e.g., heart failure, arrhythmia, ischaemic heart disease, anxiety/depression, obesity, thyroid disease, asthma, osteoporosis, generalised artherosclerosis and chronic liver disease. Smoking-related inflammation is postulated as a possible cause of many of these diseases [7].

While other studies have addressed the problem of comorbidity in patients with COPD, most have focused on a few isolated diseases. We, in contrast, studied the association between COPD and a further 25 chronic diseases. We found three studies which analysed the association between COPD and a long list of diseases in primary care patients but, as in the case of other comorbidity studies, comparison was hindered by methodological differences, in that two were based on data from ongoing records kept by volunteer physicians [27, 28] and the third used data drawn from EMRs [29]. All three used the same case definition as ours, namely, COPD recorded by a FP. Results were controlled for age in only one study [27]. Although the disease list used was not the same throughout, there was a substantial core group of diseases that was common to all the studies, including ours. As in our case, the other three studies also observed a high prevalence of cardiovascular diseases and osteoporosis.

COPD patients who also present with cardiovascular diseases register more episodes of COPD exacerbation, more hospital admissions, a notable increase in cost of medical care [30] and higher cardiovascular disease mortality [31]. In our case, 16% of patients presented with arrhythmia, 8.5% with ischaemic heart disease, and a further 8% with heart failure. This association has been reported in other studies [32]. In a study focusing on family practices in Spain, de Miguel found that prevalence of heart disease among COPD patients was 19% [8].

As reported by most studies [8, 3234], cardiovascular risk factors, such as arterial hypertension, lipid metabolism disorders, diabetes and obesity, are among the most prevalent diseases in COPD patients. This, however, is due to the ageing of patients, since, once age had been controlled for, prevalence did not prove very different to what might have been expected (Table 4). This finding indicates that, when studying the association between COPD and cardiovascular diseases, the confounding role of risk factors must be taken into account [33].

We observed 89% more chronic liver diseases than expected in a general population of this age and sex. This association has been little described but a Japanese-based study, targeting family medicine offices attended by specialist physicians [35], reported an elevated prevalence of chronic liver disease, chronic hepatitis C, hepatic steatosis and alcoholic hepatitis. Another study [36] similarly observed this association between liver disease and COPD, after controlling for age, sex and smoking habit. In addition, COPD has been described as having a swifter progression in hepatitis C patients [37]. Although, the aetiopathogenic mechanisms of this association are unclear, an interleukin-8 mediated chronic inflammatory process is suspected as being the cause [38].

Furthermore, 7% of COPD patients have osteoporosis, with a frequency that is 10 times greater in women than in men, and an observed prevalence that is higher than expected for patients of their age and sex. Some studies report patients with COPD as having a threefold risk of presenting with osteoporosis [19, 21]. Since a number of studies have shown that inhaled corticoids have no effect on bone density, other factors, such as reduced mobility, smoking habit or adverse effects of other drugs, may be the cause of this.

Anxiety and depression are frequent among patients with COPD. In our study, 20% of patients presented with these problems, with a frequency that was twice as high in women as in men. In one review, prevalence varied widely between some studies and others, due in part to the measurement instrument used and type of patient studied. Among stable patients, prevalence of depression ranged from 10% to 42% and prevalence of anxiety from 10% to 19% [39]. Our data are in line with those published. The causes for the increase in affective disorders in these patients are uncertain but, in addition to the reactive effect due to deterioration in the state of health, nicotine dependence may play an important role [40].

Six per cent of our patients had COPD and asthma, with a frequency that was more than three times higher in women than in men. This prevalence is lower than that observed in population-based studies [41], a finding probably explained by the same type of underdiagnosis as that which affects COPD. This overlapping of diseases in the same patient represents a diagnostic and therapeutic challenge for FPs [42, 43].

This study suffers from some limitations: firstly, there are those inherent in any retrospective design which uses EMRs as its data source. As a data source, medical records introduce biases stemming from under-registration and the poor quality of the data recorded [44]. In an attempt to solve this problem, physicians were selected according to the quality of their records.

Another limitation derives from the case-definition criterion used, i.e., the need for patients’ clinical histories to show evidence of diagnosis of COPD, since FPs are well known for making little use of spirometry and for misclassifying COPD patients [45]. However, in view of the fact that this was a chronic disease and of the longitudinal nature of primary care, it is likely that underdiagnosis involved the milder forms of COPD [22, 46] and that misclassification was due to COPD being diagnosed as asthma and vice-versa.

Conclusions

COPD is pathology with high sanitary, social and economic impact. Patients suffering COPD present high co morbidity associated to other pathologies of high impact on healthcare services; as a consequence COPD patients stratification should regard the comorbidity burden in addition to the degree of obstruction.

The clinical practice guidelines that are in place are targeted at isolated diseases and do not envisage the existence of comorbidity. Moreover, the healthcare delivery models based on diseases management offer a poor response to comorbidity problem and tend to fragment the assistance to the patient inciding negatively on healthcare services [47]. In addition, the emerging healthcare model based on telemonitoring and treatment “is going home” [48], and providers of such care need to customise services involved in following up and monitoring chronically ill patients in their homes. Consequently, comorbidity poses a challenge for the care of COPD patients, and so studies are needed that will help specify these different patient profiles.

In view of the results of this study, there is a need for improving the diagnosis of COPD in family practices, there is a need for clinical practice guidelines to be reviewed and rendered patient- rather than disease-oriented [49]. Similarly there is a need to adapt patient telemonitoring programmes and applications [48], as well as care-delivery models in general, so that these can adopt an integrated approach patient-centered, based on longitudinal care and co-ordination.

Ethics approval

All patient registration data were treated confidentially pursuant to the Spanish 1999 Personal Data Protection Act (Ley Orgánica de Protección de Data de Carácter Personal). The data were organised in a database and made available for analysis in this project and for research in future projects.

Patients were registered by age and sex only. No electronic patient identifier was used, and there was no information that could be used to identify individual registry patients by personalised analysis of the data. Participants’ identity was deemed confidential.

Abbreviations

ACG:

Adjusted clinical groups

CI:

Confidence interval

COPD:

Chronic obstructive pulmonary disease

EDC:

Expanded diagnosis clusters

EMR:

Electronic medical record

FP:

Family physician

GOLD:

Global strategy for diagnosis, management, and prevention of COPD

HP/HI:

High prevalence/ high impact

RUB:

Resource utilisation bands.

References

  1. Mathers CD, Loncar D: Projections of global mortality and burden of disease from 2002 to 2030. PLoS Med. 2006, 3: e442-10.1371/journal.pmed.0030442.

    Article  PubMed  PubMed Central  Google Scholar 

  2. Halbert RJ, Natoli JL, Gano A, Badamgarv E, Buist AS, Manino DM: Global burden of COPD: systematic review and meta-analysis. Eur Respir J. 2006, 28: 523-532. 10.1183/09031936.06.00124605.

    Article  CAS  PubMed  Google Scholar 

  3. Soriano JB, Ancochea J, Miratvilles M, García-Ríos F, Durán-Tauleria E, Muñoz L, Jiménez-Ruiz CA, Masa JF, Viejo JL, Villasante C, Fernández-Fau L, Sánchez G, Sobradillo-Peña V: Recent trends in COPD prevalence in Spain: a repeated cross-sectional survey 1997–2007. Eur Respir J. 2010, 36: 758-765. 10.1183/09031936.00138409.

    Article  CAS  PubMed  Google Scholar 

  4. Fortin M, Lapointe LA, Hudon C, Vanasse A: Multimorbidity is common to family practice. Is it commonly researched?. Can Fam Physician. 2005, 51: 244-250.

    PubMed  Google Scholar 

  5. Laux G, Kuehlein T, Rosemann T, Szecsenyi J: Co- and multimorbidity patterns in primary care based on episodes of care: results from the German CONTENT project. BMC Health Serv Res. 2008, 8: 14-21. 10.1186/1472-6963-8-14.

    Article  PubMed  PubMed Central  Google Scholar 

  6. Global Initiative for chronic obstructive lung disease: Global strategy for the diagnosis, management and prevention of chronic obstructive pulmonary disease (revised 2011). 2011, Bethesda: National Herat, Lung and Blood Institute, http://www.goldcopd.org. Date accessed 23 January 2012

    Google Scholar 

  7. Bornes PJ, Celli BR: Systemic manifestations and comorbidities of COPD. Eur Respir J. 2009, 33: 1165-1185. 10.1183/09031936.00128008.

    Article  Google Scholar 

  8. de Miguel D, Carrasco Garrido P, Rejas Gutiérrez J, Martín Centeno A, Gobartt Vázquez E, Hernández Barreda V, et al: The influence of heart disease on caharcteristics, quality of life, use of Elath resources, and costs of COPD in primary care settings. BMC Cardiovasc Disord. 2010, 10: 8-10.1186/1471-2261-10-8.

    Article  PubMed  PubMed Central  Google Scholar 

  9. Yeo J, Karimova G, Bansal S: Co-morbidity in older patients with COPD – its impact on health service utilization and quality of life, a community study. Age Ageing. 2006, 35: 33-37. 10.1093/ageing/afj002.

    Article  CAS  PubMed  Google Scholar 

  10. Menzin J, Boulanger L, Marton J, Guadagno L, Dastani H, Dirani R, et al: The economic burden of chronic obstructive pulmonary disease (COPD) in a U.S. medicare population. Respir Med. 2008, 102: 1248-1256. 10.1016/j.rmed.2008.04.009.

    Article  PubMed  Google Scholar 

  11. Sin DD, Anthonisen NR, Soriano JB, Agusti AG: Mortality in COPD: role of comorbidities. Eur Respir J. 2006, 28: 1245-1257. 10.1183/09031936.00133805.

    Article  CAS  PubMed  Google Scholar 

  12. Boyd CM, Darer J, Boult C, Fried LP, Boult L, Wu AW: Clinical practice guidelines and quality of care for older patients with multiple comorbid diseases. Implications for pay for performance. JAMA. 2005, 294: 716-724. 10.1001/jama.294.6.716.

    Article  CAS  PubMed  Google Scholar 

  13. Van den Akker M, Buntinx F, Metsemakers JFM, Roos S, Knottnerus JA: Multimorbidity in general practice: prevalence, incidence and determinants of co-occurring chronic and recurrent diseases. J Clin Epidemiol. 1998, 51: 367-375. 10.1016/S0895-4356(97)00306-5.

    Article  CAS  PubMed  Google Scholar 

  14. Weiner JP: The Johns Hopkins ACG® Case Mix System. Reference manual. Version 7. 2005, Baltimore: The Johns Hopkins University. Bloomberg School of Public Health

    Google Scholar 

  15. Prosser R, Carleton B, Smith A: The comorbidity burden of the treated asthma patient population in British Columbia. Chronic Dis Can. 2010, 30: 46-55.

    CAS  PubMed  Google Scholar 

  16. Broemeling AM, Watson D, Black C: Chronic conditions and co-morbidity among residents of British Columbia. 2005, Vancouver BC: Centre for Health Services and Policy Research

    Google Scholar 

  17. Carlsson L: Patient based “burden-of-illness” in Swedish primary health care. Applying the Johns Hopkins ACG case-mix system in a retrospective study of electronic patient records. Int J Health Plann Manage. 2002, 17: 268-282.

    Article  Google Scholar 

  18. Juncosa S, Bolibar B, Roset M, Tomas R: Performance af an ambulatory casemix measurement system in primary care in Spain: ambulatory care groups (ACGs). Eur J Public Health. 1999, 9: 27-35. 10.1093/eurpub/9.1.27.

    Article  Google Scholar 

  19. O’Halloran J, Miller GC, Britt H: Defining chronic conditions for primary care with ICPC – 2. Fam Pract. 2004, 21: 381-386. 10.1093/fampra/cmh407.

    Article  PubMed  Google Scholar 

  20. Miratvilles M, Soriano JB, García Río F, Muñoz L, Durán Taulería E, Sánchez G, et al: Prevalence of COPD in Spain: impacto f undiagnosed COPD on quality of life and daily life activities. Thorax. 2009, 64: 863-868. 10.1136/thx.2009.115725.

    Article  Google Scholar 

  21. Takahashi T, Ichinose M, Inoue H, Shirato K, Hattori T, Takishima T: Underdiagnosis and undertreatment of COPD in primary care settings. Respirology. 2003, 8: 504-508. 10.1046/j.1440-1843.2003.00501.x.

    Article  PubMed  Google Scholar 

  22. Sandelowsky H, Ställberg B, Nager A, Hasselström J: The prevalence of undiagnosed chronic obstructive pulmonary disease in primary care population with respiratory tract infections – case finding study. BMC Fam Pract. 2011, 12: 122-10.1186/1471-2296-12-122.

    Article  PubMed  PubMed Central  Google Scholar 

  23. Feary JR, Rodrigues LC, Smith CJ, Hubbard RB: Prevalence of major comorbidities in subjects with COPD and incidence of myocardial infarction and stroke: a comprehensive analysis using data from primary care. Thorax. 2010, 65: 956-962. 10.1136/thx.2009.128082.

    Article  PubMed  Google Scholar 

  24. Miratvilles M, de la Roza C, Morera J, Montemayor T, Gobbart E, Martin A, Álvarez Sala JL: Chronic respiratory symptoms, spirometry and knowledge of COPD among general population. Respir Med. 2006, 100: 1973-1980. 10.1016/j.rmed.2006.02.024.

    Article  Google Scholar 

  25. Cazzola M, Bettoncelli G, Sessa E, Cricelli C: Primary care of patients with chronic obstructive pulmonary disease in Italy. Respir Med. 2009, 103: 582-588. 10.1016/j.rmed.2008.10.017.

    Article  PubMed  Google Scholar 

  26. Walters JA, Hansen EC, Walters EH, Wood-Baker R: Under – diagnosis of chronic obstructive pulmonary disease: a qualitative study in primary care. Respir Med. 2008, 102: 738-743. 10.1016/j.rmed.2007.12.008.

    Article  PubMed  Google Scholar 

  27. Soriano JB, Visick GT, Muellerova H, Payvandi N, Hansell AL: Patterns of comorbidities in newly diagnosed COPD and asthma in primary care. Chest. 2005, 128: 2099-2107. 10.1378/chest.128.4.2099.

    Article  PubMed  Google Scholar 

  28. Cazzola M, Bettoncelli G, Sessa E, Cricelli C, Biscione G: Prevalence of comorbidities in patients with chronic obstructive pulmonary disease. Respiration. 2010, 80: 112-119. 10.1159/000281880.

    Article  PubMed  Google Scholar 

  29. Buffels J, Degryse J, Liistro G: Diagnostic certainty, co – morbidity and medication in primary care population with presumed airway obstruction: the DIDASCO2 study. Prim Care Resp J. 2009, 18: 34-40. 10.3132/pcrj.2008.00047.

    Google Scholar 

  30. Holguin F, Folch E, Redd SC, Manino DM: Comorbidity and mortality in COPD – related hospitalizations in the United States, 1979 to 2001. Chest. 2005, 128: 2005-2011. 10.1378/chest.128.4.2005.

    Article  PubMed  Google Scholar 

  31. Dalal AA, Shah M, Lunacsek O, Hanania NA: Clinical and economic burden of patients diagnosed with comorbid cardiovascular disease. Respir Med. 2011, 105: 1516-1522. 10.1016/j.rmed.2011.04.005.

    Article  PubMed  Google Scholar 

  32. Curkendall SM, DeLuise C, Jones JK, Lanes S, Stang MR, Goehring E, et al: Cardiovascular disease in patients with chronic obstructive pulmonary disease, Saskatchewan Canada cardiovascular disease in COPD patients. Ann Epidemiol. 2006, 16: 63-70. 10.1016/j.annepidem.2005.04.008.

    Article  PubMed  Google Scholar 

  33. Izquierdo JL, Martínez A, Guzmán E, de Lucas P, Rodríguez JM: Lack of association of ischemic heart disease wihth COPD when taking into account classical cardiovascular risk factors. Int J Chron Obstruct Pulmon Dis. 2010, 5: 387-394.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  34. de Lucas P, Izquierdo JL, Rodríguez JM, Bellón JM, Ancoechea J, Calle M, et al: Asociación de factores de riesgo cardiovascular y EPOC. Resultados de un estudio epidemiológico (estudio ARCE). Arch Bronconeumol. 2008, 44: 233-238.

    Google Scholar 

  35. Minakata Y, Sigiura H, Yamegata T, Yanagisewa S, Ichikawa T, Koarai A, et al: Prevalence of COPD in primary care clinics: correlation with non – respiratory diseases. Intern Med. 2008, 47: 77-82. 10.2169/internalmedicine.47.0489.

    Article  PubMed  Google Scholar 

  36. Minakata Y, Ueda H, Akamatsu K, Kanda M, Yanagisawa S, Ichikawa T, et al: High COPD prevalence in patients with liver disease. Intern Med. 2010, 49: 2687-2691. 10.2169/internalmedicine.49.3948.

    Article  PubMed  Google Scholar 

  37. Kanazawa H, Hirata K, Yoshikawa J: Accelerated decline of lung function in COPD patients with chronic hepatitis C virus infection: a preliminary study based on small number of patients. Chest. 2003, 123: 596-599. 10.1378/chest.123.2.596.

    Article  PubMed  Google Scholar 

  38. Moorman JP, Fitzgerald SM, Prayther DC, Lee SA, Chi DS, Krisnaswamy G: Induction of p38- gC1qR-dependent IL-8 expression in pulmonary fibroblasts by soluble hepatitis C core protein. Respir Res. 2005, 6: 105-116. 10.1186/1465-9921-6-105.

    Article  PubMed  PubMed Central  Google Scholar 

  39. Maurer J, Rebbapragada V, Borson S, Goldstein R, Kunik ME, Yohannes AM, Hanania NA: Anxiety and depression in COPD: current understanding, unanswered questions, and research needs. Chest. 2008, 134: 43S-56S. 10.1378/chest.08-0342.

    Article  PubMed  PubMed Central  Google Scholar 

  40. Goodwin RD, Lavoie KL, Lemeshow AR, Jenkins E, Brown ES, Fedoronko DA: Depression, anxiety and COPD: the unexamined role of nicotine dependence. Nicotine Tob Res. 2012, 14: 176-183. 10.1093/ntr/ntr165.

    Article  PubMed  Google Scholar 

  41. Soriano JB, Davis JK, Coleman B, Visick G, Mannino D, Pride NB: The proportional venn diagram of obstructive lung disease: two approximations from the United States and the United Kingdom. Chest. 2003, 124: 474-481. 10.1378/chest.124.2.474.

    Article  PubMed  Google Scholar 

  42. Tinkelman DG, Price DB, Nordyke RJ, Halbert RJ: Misdiagnosis of COPD and asthma in primary care patients 40 years of age and over. J Asthma. 2006, 43: 75-80. 10.1080/02770900500448738.

    Article  PubMed  Google Scholar 

  43. Fromer L: Diagnosing and treating COPD: understanding the challenge and finding solutions. Intern J Gen Med. 2011, 4: 729-739.

    Google Scholar 

  44. Jordan K, Porcheret M, Croft P: Quality of morbidity coding in general practice computerized medical record: a systematic review. Fam Pract. 2004, 21: 396-412. 10.1093/fampra/cmh409.

    Article  PubMed  Google Scholar 

  45. De Miguel Díez J, Izquierdo Alonso JL, Molina París J, Rodríguez González Moro JM, de Lucas Ramos P, Gaspar Alonso Vega G: Fiabilidad del diagnóstico de la EPOC en atención primaria y neumología en España. Factores predictores. Arch Bronconeumol. 2003, 39: 203-208. 10.1157/13047333.

    PubMed  Google Scholar 

  46. Lindberg A, Bjerg-Baäcklund A, Rönmark E, Larsson LG, Lundbäck B: Prevalence and underdiagnosis of COPD by disease severity and the attributable fraction of smoking. Report from the obstructive lung disease in northern Sweden SDtudies. Respir Med. 2006, 100: 264-272. 10.1016/j.rmed.2005.04.029.

    Article  PubMed  Google Scholar 

  47. Liu CW, Einstadter D, Cebul RD: Care fragmentation and emergency department use among complex patient with diabetes. Am J Manag Care. 2010, 16: 413-420.

    CAS  PubMed  Google Scholar 

  48. Ekeland AG, Bowes A, Flottorp S: Effectiveness of telemedicine: a systematic review of reviews. Int J Med Inform. 2010, 79: 736-771. 10.1016/j.ijmedinf.2010.08.006.

    Article  PubMed  Google Scholar 

  49. Dawes M: Co–morbidity: we need a guideline for each patient not a guideline for each disease. Fam Pract. 2010, 27: 1-2. 10.1093/fampra/cmp106.

    Article  PubMed  Google Scholar 

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Acknowledgements

The authors would like to express their gratitude for the support, help and consent received from the Madrid Area 11 Primary Care Administration.

This study was partially supported by the National Strategic Consortia for Technical Research (CENIT) Programme funded by the Centre for the Development of Industrial Technology (CDTI)/Ministry of Science and Innovation (MICINN) [CEN-2007-1010 “Digital personal environment for health and wellbeing – AmiVital” project], a grant from the Ministry of Health & Consumer Affairs [FIS PI09-01787 “Spanish Cohort of Patients with Advanced COPD: Phenotypic Heterogeneity and clinical evolution”]. The funders had no role in the study design, data-collection and -analysis, decision to publish, or drafting of the manuscript.

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Correspondence to Luis García-Olmos.

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Competing interests

L. García-Olmos, A. Alberquilla, P. García-Sagredo, L. Morales, M. Carmona, M.J. de Tena-Dávila, M. Pascual, A. Muñoz, C.H. Salvador and J.L. Monteagudo declare that they have no conflicts of interest.

V. Ayala is an employee of Praxair España.

Authors’ contributions

LG-O, AA and VA contributed to the study design. CHS and LG-O conceived the study. AA, PG-S, MC and CHS supervised the study. AA, MP and AM assessed procedures and built a database. AA, PG-S, MC and MJdT-D analysed the data. LG-O, VA and LM wrote the first and last drafts of the manuscript. All authors contributed ideas, revised different drafts of the manuscript and approved the final version.

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García-Olmos, L., Alberquilla, Á., Ayala, V. et al. Comorbidity in patients with chronic obstructive pulmonary disease in family practice: a cross sectional study. BMC Fam Pract 14, 11 (2013). https://doi.org/10.1186/1471-2296-14-11

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  • DOI: https://doi.org/10.1186/1471-2296-14-11

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