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Novel Approach to the Treatment in Rheumatic Diseases: From Molecule to Value for Patient

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Volume 2018 |Article ID 7458361 |

Cătălin Codreanu, Claudiu C. Popescu, Corina Mogoşan, "Area of Residence and Socioeconomic Factors Reduce Access to Biologics for Rheumatoid Arthritis Patients in Romania", BioMed Research International, vol. 2018, Article ID 7458361, 8 pages, 2018.

Area of Residence and Socioeconomic Factors Reduce Access to Biologics for Rheumatoid Arthritis Patients in Romania

Academic Editor: Ewa Mojs
Received20 Dec 2017
Accepted29 Mar 2018
Published08 May 2018


Introduction. The study aimed to evaluate the influence of socioeconomic factors on rheumatoid arthritis (RA) patients’ access to biologics in Romania. Method. Cross-sectional data were collected in January 2014 from the Romanian Registry of Rheumatic Diseases (RRRD) comprising all RA patients on biologics from 42 Romanian counties. “Territorial” access to biologics was defined by patients receiving biologics in their home county. A county was “equitable” if <25% of RA patients received biologics outside it. Results. The RRRD included 4507 RA patients aged years, with a disease duration of years. Urban dwellers (67.8%) had a significantly higher prevalence of territorial biologic access than rural dwellers (83.1% compared to 74.1%; ). Gross domestic product (GDP) in 1000 €/capita/county (odds ratio (OR) = 1.224) and number of physicians/1000 inhabitants/county (OR = 2.198) predict territorial access to biologics and also predict the number of territorially treated RA patients. Inequitable counties exhibited significantly lower socioeconomic indicators than equitable counties. Conclusion. In Romania, RA patients’ access to biologics varies significantly between counties. Urban dwellers and patients living in counties/regions with high living standards are more likely to receive biologics locally than those living in more deprived areas.

1. Introduction

Rheumatoid arthritis (RA) is a systemic inflammatory autoimmune disorder affecting approximately 1% of the general population [1]. Recent epidemiological data show an increase in disease incidence in women in the past ten years [2]. RA can lead to functional disability, low quality of life, increased morbidity, and mortality [3].

Since RA usually affects professionally active people, it has important economic consequences, adding costs to patients and their families and to society through extensive use of health resources and loss of work productivity [4, 5]. The main goal of RA treatment is to induce and maintain remission whenever possible, or at least low disease activity [6]. Biological disease modifying antirheumatic drugs (bDMARDs) have revolutionized the therapy of RA and their efficacy is largely documented in clinical trials worldwide [79]. However, the high cost of bDMARDs is limiting their use, particularly in developing countries (since 2000, the Romanian public healthcare system reimburses adalimumab, etanercept, infliximab original and biosimilar, and rituximab, and since 2015 it also reimburses abatacept, certolizumab, golimumab, and tocilizumab).

In order to be eligible for bDMARDs in Romania, RA patients must be nonresponders to two different conventional synthetic DMARDs (csDMARDs) just like in other European countries, but they must fulfill other severity criteria which are stricter [10]. While some European countries do not reimburse bDMARDs yet, others offer free prescription, regardless of disease duration and previous therapies [10]. In 2011, among Central and Eastern European countries, Romania had the fifth highest prevalence of bDMARDs treatment among RA patients (2.2%) [11]. This variation of bDMARD uptake in Europe is coupled with observational evidence that socioeconomic status, area of residence, and income influence disease activity, disease outcome, and treatment access [1215], which shows that significant inequities exist among different European countries with respect to RA management. Therefore, it is reasonable to hypothesize that these same limiting factors also create inequities at a national level especially because the regions of Romania differ in terms of socioeconomic and development characteristics. The Romanian territory is divided into 4 macroregions, 2 regions, and 42 counties: macroregion 1 consists of the Northwest (6 counties) and Center (6 counties) regions; macroregion 2 consists of Northeast (6 counties) and Southeast (6 counties) regions; macroregion 3 consists of South (6 counties) and Capital (2 counties) regions; macroregion 4 consists of Southwest (5 counties) and West (4 counties) regions. Historically and economically, macroregions 1 and 3 are the most developed areas of Romania, while macroregions 2 and 4 are significantly below the European Union’s mean. This uneven distribution could hypothetically generate similar differences regarding access of RA patients to expensive medication (biologics). In this context, the study aims to evaluate the influence of socioeconomic factors on RA patients’ access to biological therapy in Romania.

2. Materials and Methods

2.1. Romanian Eligibility Criteria for bDMARD Therapy in RA

In order to be considered for bDMARDs therapy, Romanian RA patients must fulfill four criteria: (a) the diagnosis of RA to be be made by a rheumatologist and it should fulfill the 2010 RA classification criteria [16]; (b) either high disease activity (HDA) irrespective of disease duration or early RA (under 2 years) with moderate disease activity (MDA) and with at least five poor prognosis factors, both with at least 5 swollen and/or tender joints and at least two of the following three criteria: morning stiffness above 60 minutes, erythrocyte sedimentation rate (ESR) above 28 mm/h, and C reactive protein (CRP) more than 3 times the upper limit of normal (ULN); (c) lack of response to at least two csDMARDs used for 12 weeks each; (d) no known contraindications for bDMARDs.

RA activity is assessed using the composite 28-joint count disease activity score (DAS28), which is based on the number of tender joints, number of swollen joints, ESR or CRP, and the visual analog scale for patient-reported general health [17]: patients with HDA have a DAS28 > 5.1, while patients with MDA have a DAS28 > 3.2.

The mentioned poor prognosis factors include age under 45 years; rheumatoid factor and/or anticitrullinated protein antibodies 10 times the ULN; ESR > 50 mm/h or CRP > 5 times the ULN; erosions on X-rays, ultrasound or magnetic resonance imaging; Health Assessment Questionnaire score above 1.5; extra-articular manifestations.

2.2. The Romanian Registry of Rheumatic Diseases (RRRD)

As soon as a patient fulfills the above criteria for bDMARDs use, the attending rheumatologist uploads the data into the RRRD, which is a national electronic database comprising all RA patients treated with biologics in Romania. Prior to treatment and inclusion in the RRRD, all patients signed an informed consent form for both bDMARD therapy and scientific use of their data.

For the purpose of this study, the variables were collected in January 2014 using a cross-sectional study design: demographics (age, sex, and area of residence) and RA-specific variables (disease duration, bDMARDs). The geographical distribution of patients (Romania has 42 administrative divisions: 41 counties and the capital) was reconfigured from a treatment perspective: if the patient received the bDMARD in home county, the case was considered “territorial” access; if the patient received the bDMARD outside home county, the case was considered “extraterritorial” access. Similarly, if a county had less than 25% of its RA patients treated outside, the county was considered to have “equitable” access; if more than 25% of its RA patients were treated outside, the county was considered to have “inequitable” access. The local and RRRD ethics committees approved the study protocol.

2.3. Socioeconomic Indicators

Socioeconomic indicators were collected from the National Institute of Statistics Yearbook (EUROSTAT [18]) and included the population distribution by county, indicators of living standards: gross domestic product (GDP) per capita per county in local currency (Romanian Leu) and Euro, physicians’ distribution nationwide and by county, and the rheumatologists’ distribution per counties.

2.4. Statistical Analysis

The normal distribution of the data was assessed using descriptive statistics, normality and stem-and-leaf plots, and the Lilliefors corrected Kolmogorov-Smirnov test. The age of the patients and their disease duration were distributed normally and therefore they were reported as “mean ± standard deviation.”

On a patient-based analysis (4507 patients), the association between residence (rural or urban) and bDMARD access (territorial and extraterritorial) was assessed using a test with a Cramer’s statistic for effect size. The differences between continuous variables (age, GDP, number of physicians, and number of rheumatologists) between patients with territorial or extraterritorial biologic access were assessed using -tests. Effect size for these -tests was calculated by Cohen’s statistic, approximated by running the -tests using the standardized values ( scores) of the independent variables and observing the mean difference output of these -tests. A binary logistic regression model was computed in order to predict the likelihood that RA patients will have territorial bDMARD access using the following predictors: age (years), area of residence (coded “0” for rural and “1” for urban), GDP (expressed in 1000 €/capita/county) and number of physicians/1000 inhabitants/county. The results were reported in terms of odds ratios (OR) with 95% confidence intervals (CI).

On a county-based analysis (42 counties), GDP/capita, number of physicians/1000 inhabitants, and number of rheumatologists/county exhibited a nonnormal distribution; therefore the differences of these scale variables according to type of county (equitable and inequitable) were studied using Mann–Whitney tests (effect size for these tests was evaluated by estimating Glass rank biserial correlations using bivariate Spearman’s correlations between the nominal and scale variables). For the same reason, the correlations between these scale variables among themselves and with the number of territorially and extraterritorially treated RA patients per county were computed using Spearman’s rho coefficients. Two hierarchical multiple linear regression models were constructed in order to predict the number of RA patients with territorial access to biologics. Both models used GDP/capita as predictor in the first step. For the second step, in the first model the number of physicians/1000 inhabitants was added as predictor, while in the second model the number of rheumatologists/county was added as predictor. These predictors were previously normalized by extracting square roots (number of rheumatologists/county) or by calculation of their natural logarithms (number of physicians/1000 inhabitants). Since the number of physicians and the number of rheumatologists are not independent variables (the number of physicians includes the number of rheumatologists), they were not included together in the same regression model.

The statistical tests were considered significant if . All the statistical analysis was done using IBM SPSS Statistics version 22.0 for Windows (Armonk, NY, IBM Corp.).

3. Results

3.1. Patient-Based Analysis

Until January 2014, the RRRD included 4507 patients with RA: 4267 (94.7%) treated with biologics and 240 (5.3%) with approved biological therapy, but treatment not yet started. The patients had a mean age of years and a mean RA duration of years. The majority of patients were women (3842 patients—85.2%) and the majority of patients lived in urban areas (3056 patients—67.8%). In the sample, 80.2% (3614) of RA patients benefited from territorial bDMARD access, while 19.8% (893) had extraterritorial bDMARD access (Figure 1, Table 1). Urban dwellers had a significantly higher prevalence of territorial bDMARD access than rural dwellers (Figure 2).

DivisionInhabitantsGDPPhysiciansRheumatologistsRA biologics

Macroregion 154685257123.22.4550872
Satu Mare3906394014.11.52245

Macroregion 267942696235.81.68641358

Macroregion 3575787110892.33.22891469

Macroregion 442210536706.52.8232868

Notes. Data from 2013; county names are in Romanian; for each county: GDP €/capita, number of physicians/1000 inhabitants, absolute number of rheumatologists, and absolute number of RA patients treated with biologics. GDP: gross domestic product; RA: rheumatoid arthritis.

Compared to RA patients with territorial bDMARD access, those with extraterritorial bDMARD access had equivalent mean ages but came from counties with significantly lower socioeconomic indicators (Figure 3).

The logistic regression model (; ) explained 32.1% of bDMARD accessibility (Nagelkerke ) and it correctly classified 81.7% of patients. Accounting for all other predictors included/present in the model, GDP expressed in 1000 €/capita/county (OR = 1.224; 95% CI: 1.186–1.263) and number of physicians/1000 inhabitants per county (OR = 2.198; 95% CI: 1.845–2.618) significantly increased the likelihood that patients will have (equitable) territorial bDMARD access.

3.2. County-Based Analysis

The majority of RA patients who are treated with bDMARDs outside their home environments chose the capital (Bucharest): 53.7% (805/1498) of patients treated in Bucharest come from a different county. Compared to equitable counties regarding bDMARD treatment, the inequitable counties exhibited significantly lower socioeconomic indicators (Figure 4).

The number of rheumatologists/county, the number of physicians/1000 inhabitants/county, and GDP/capita were significantly and positively correlated with the number of territorially treated RA patients/county (rho = 0.843, ; rho = 0.448, ; rho = 0.337, , resp.), and they were significantly and negatively correlated with the number of extraterritorially treated RA patients/county (rho = −0.340, ; rho = −0.410, ; rho = −0.337, resp.).

The distribution of socioeconomic indicators among counties was uneven in terms of number of rheumatologists/county (mean = 5.6; median = 2.0; skewness = 4.84; kurtosis = 26.2; minimum = 0; maximum = 75), the number of physicians/1000 inhabitants/county (mean = 2.01; median = 1.52; skewness = 2.13; kurtosis = 4.48; minimum = 1; maximum = 6.02), and GDP/capita (mean = 4824 €; median = 4299 €; skewness = 2.48; kurtosis = 8.25; minimum = 2535 €; maximum = 13575 €).

Two hierarchical regression analysis models were computed to predict the number of territorially treated RA patients using GDP (1000 €/capita/county) in the first step and then adding either the number of physicians/1000 inhabitants/county or the number of rheumatologists/county as predictors (Table 2). GDP on its own significantly explained 43.4% of the variance of territorially treated RA patients. Adding either the number of physicians/1000 inhabitants/county or the number of rheumatologists/county produced significant models in which these variables predicted an additional 22.3% and 46.8%, respectively, in the variance of territorially treated RA patients. In both models GDP became an insignificant predictor when both independent variables (GDP and number of physicians or GDP and number of rheumatologists) were entered into the regression model, an observation explained by the degree of correlations of GDP with the number of physicians/1000 inhabitants/county (rho = 0.731; ) and with the number of rheumatologists/county (rho = 0.438; ).

GDPGDP + physiciansGDP + rheumatologists


Notes. GDP was expressed per 1000 €/capita/county; the number of physicians was expressed per 1000 inhabitants/county; the number of rheumatologists was expressed per county; there are 2 models: model 1 (GDP at the first step, GDP and physicians at the second step); model 2 (GDP at the first step, GDP and rheumatologists at the second step). GDP: gross domestic product; RA: rheumatoid arthritis.

4. Discussion

The aim of the study was to assess the impact of socioeconomic factors on Romanian RA patients’ accessibility to bDMARDs. In this sense, we found that rural habitat and poor county socioeconomic indicators (GDP/capita, number of physicians/1000 inhabitants, and number of rheumatologists/county) are associated with lower access to bDMARDs. In order to discuss the relevance of these results, we must first review the characteristics of the sample. Compared to patients from other European RA registries [19], RA patients from the RRRD have an equivalent mean age, the same form of established disease according to disease duration, but a higher prevalence of female patients. In the absence of conclusive epidemiological studies of RA in Romania, this observation may be explained by a number of competing reasons: underdiagnosis of men; higher disease severity among women requiring biological therapy; a hypothesized genetic population trait. Detailed prevalence studies are needed to assess these possibly non-mutually exclusive hypotheses.

Observational studies have reported that financial factors such as macroeconomic conditions, income, and national health expenditure are major influencing factors of bDMARD accessibility in European countries [11, 15, 2023]. Even though these studies made observations by comparing different countries, it is reasonable to expect that the same financial factors influence bDMARD accessibility of RA patients within different regions of the same country, given the existence of macroeconomic heterogeneity between these regions. As EUROSTAT data show, the 41 counties and the capital of Romania display an important amount of GDP/capita heterogeneity. Given these significant differences of GDP/capita among Romanian counties, we indeed showed that low GDP/capita predicts low bDMARD access. Furthermore, even though national guidelines attempt to create equal opportunities in terms of access to biologic therapy for all eligible RA patients, in practice many patients need to travel to another county in order to benefit from bDMARDs. Finally, following its highest GDP/capita among counties, we observed a strong centralizing effect of the capital on the number of RA patients treated with bDMARDs, a tendency noted by other authors in the literature [24]. Since every county has its own Health Insurance House which reimburses treatment cost, a revision of the distribution of funds would possibly increase accessibility to bDMARDs outside the capital.

The observed predictive power of the number of physicians/rheumatologists for bDMARD access of RA patients is intrinsically linked to the characteristics of the disease and the structure of the health system. In this sense, the number of physicians has been long used as an indicator of socioeconomic development. Nationwide, for a population of roughly twenty million inhabitants, there were 235 active rheumatologists. Out of the 42 administrative divisions of Romania, there were 7 counties without a rheumatologist, while in the capital there were 75 active rheumatologists. The distribution of rheumatologists among the 41 counties and the capital was uneven and it was correlated with territorial economic level, as measured by the GDP/county (rho = 0.731; ). While other more economically developed countries are also facing a shortage of rheumatologists [25, 26], the proportions are very different. The lack of specialized healthcare professionals in rheumatology leads to known barriers to bDMARD therapy in RA, such as long waiting time for medical visits and travel difficulties related to long distances to rheumatology clinical settings [27, 28]. A study investigating patient-reported barriers to access bDMARD treatment in Romanian RA patients would assess the full extent of the issue.

There are some limitations of this study which could influence interpretation of the results. There were no data regarding educational status (a known influencing factor of bDMARD access) [15] and the actual extent of disease activity above the protocol cutoff (DAS > 5.1). A geographical confounder, which we were unable to control, can be described, namely, the travel distances to clinics between different counties: these must have been patients who lived very close to county borders and therefore their extraterritorial bDMARD access could have been a matter of convenience. Additional variables (such as socioeconomic status of each patient and the number of patients who did not receive biologics because of travelling limitations) were not collected. All the analyzed variables came from different contributors to the RRRD (the attending rheumatologists) and their quality relies on the assumption of correct data input into the national electronic system.

5. Conclusions

In Romania, accessibility of RA patients to biological therapy varies significantly between different counties. Areas with low socioeconomic level do not offer equal and fair therapeutic opportunities for RA patients compared to other national areas: patients with RA living in urban areas and counties/regions with high living standards are more likely to receive biological agents locally than those living in more deprived areas. Studies investigating patient-reported barriers to biologic therapy are needed in the Romanian population.

Conflicts of Interest

The authors declare no conflicts of interest.


The authors would like to acknowledge the support of the Romanian Registry of Rheumatic Diseases, which uses unrestricted grants from AbbVie, Pfizer, MSD, Roche, UCB, and BMS.


  1. W. Grassi, R. De Angelis, G. Lamanna, and C. Cervini, “The clinical features of rheumatoid arthritis,” European Journal of Radiology, vol. 27, no. 1, pp. S18–S24, 1998. View at: Publisher Site | Google Scholar
  2. E. Myasoedova, C. S. Crowson, H. M. Kremers, T. M. Therneau, and S. E. Gabriel, “Is the incidence of rheumatoid arthritis rising? results from olmsted county, Minnesota, 1955–2007,” Arthritis and Rheumatology, vol. 62, no. 6, pp. 1576–1582, 2010. View at: Publisher Site | Google Scholar
  3. A. Carreño, I. Fernández, X. Badia, C. Varela, and M. Roset, “Using HAQ-DI to estimate HUI-3 and EQ-5D utility values for patients with rheumatoid arthritis in Spain,” Value in Health, vol. 14, no. 1, pp. 192–200, 2011. View at: Publisher Site | Google Scholar
  4. T. Sokka, “Work disability in early rheumatoid arthritis,” Clinical and Experimental Rheumatology, vol. 21, no. 5, pp. S71–S74, 2003. View at: Google Scholar
  5. S. M. Verstappen, J. W. Bijlsma, H. Verkleij et al., “Overview of work disability in rheumatoid arthritis patients as observed in cross-sectional and longitudinal surveys,” Arthritis and Rheumatism, vol. 51, no. 3, pp. 488–497, 2004. View at: Publisher Site | Google Scholar
  6. J. S. Smolen, R. Landewe, F. C. Breedveld et al., “EULAR recommendations for the management of rheumatoid arthritis with synthetic and biological disease-modifying antirheumatic drugs: 2013 update,” Annals of the Rheumatic Diseases, vol. 73, no. 3, pp. 492–509, 2013. View at: Google Scholar
  7. A. Pierreisnard, N. Issa, T. Barnetche, C. Richez, and T. Schaeverbeke, “Meta-analysis of clinical and radiological efficacy of biologics in rheumatoid arthritis patients naive or inadequately responsive to methotrexate,” Joint Bone Spine, vol. 80, no. 4, pp. 386–392, 2013. View at: Publisher Site | Google Scholar
  8. J. A. Singh, R. Christensen, G. A. Wells et al., “A network meta-analysis of randomized controlled trials of biologics for rheumatoid arthritis: a Cochrane overview,” Canadian Medical Association Journal: Journal De L'association Medicale Canadienne, vol. 181, no. 11, pp. 787–796, 2009. View at: Publisher Site | Google Scholar
  9. J. A. Singh, A. Hossain, E. Tanjong Ghogomu et al., “Biologics or tofacitinib for rheumatoid arthritis in incomplete responders to methotrexate or other traditional disease-modifying anti-rheumatic drugs: A systematic review and network meta-analysis,” Cochrane Database of Systematic Reviews, vol. 2016, no. 5, Article ID CD012183, 2016. View at: Publisher Site | Google Scholar
  10. P. Putrik, “Variations in criteria regulating treatment with reimbursed biologic DMARDs across European countries. Are differences related to country's wealth?” Annals of the Rheumatic Diseases, vol. 73, no. 11, pp. 2010–2021, 2014. View at: Publisher Site | Google Scholar
  11. E. Orlewska, I. Ancuta, B. Anic et al., “Access to biologic treatment for rheumatoid arthritis in Central and Eastern European (CEE) countries,” Medical Science Monitor: International Medical Journal of Experimental and Clinical Research, vol. 17, no. 4, pp. SR1–SR13, 2011. View at: Publisher Site | Google Scholar
  12. L. Massardo, B. A. Pons-Estel, D. Wojdyla et al., “Early rheumatoid arthritis in Latin America: low socioeconomic status related to high disease activity at baseline,” Arthritis care and research, vol. 64, no. 8, pp. 1135–1143, 2012. View at: Google Scholar
  13. D. P. M. Symmons, “Environmental factors and the outcome of rheumatoid arthritis,” Best Practice & Research Clinical Rheumatology, vol. 17, no. 5, pp. 717–727, 2003. View at: Publisher Site | Google Scholar
  14. L. F. Callahan and T. Pincus, “Formal education level as a significant marker of clinical status in rheumatoid arthritis,” Arthritis and Rheumatism, vol. 31, no. 11, pp. 1346–1357, 1988. View at: Publisher Site | Google Scholar
  15. P. Putrik, S. Ramiro, A. P. Keszei et al., “Lower education and living in countries with lower wealth are associated with higher disease activity in rheumatoid arthritis: Results from the multinational COMORA study,” Annals of the Rheumatic Diseases, vol. 75, no. 3, pp. 540–546, 2016. View at: Publisher Site | Google Scholar
  16. D. Aletaha, T. Neogi, and A. J. Silman, “2010 rheumatoid arthritis classification criteria: an american college of rheumatology/european league against rheumatism collaborative initiative,” Annals of the Rheumatic Diseases, vol. 69, no. 9, pp. 1580–1588, 2010. View at: Publisher Site | Google Scholar
  17. M. L. Prevoo, M. A. van 't Hof, H. H. Kuper, M. A. van Leeuwen, L. B. van de Putte, and P. L. van Riel, “Modified disease activity scores that include twenty-eight-joint counts: development and validation in a prospective longitudinal study of patients with rheumatoid arthritis,” Arthritis & Rheumatology, vol. 38, no. 1, pp. 44–48, 1995. View at: Publisher Site | Google Scholar
  18. “Statistica INd,” View at: Google Scholar
  19. J. R. Curtis, A. Jain, J. Askling et al., “A comparison of patient characteristics and outcomes in selected European and U.S. rheumatoid arthritis registries,” Seminars in Arthritis and Rheumatism, vol. 40, no. 1, pp. 2–14, 2010. View at: Publisher Site | Google Scholar
  20. J. M. Hoebert, A. K. Mantel-Teeuwisse, L. van Dijk, J. W. J. Bijlsma, and H. G. M. Leufkens, “Do rheumatoid arthritis patients have equal access to treatment with new medicines? Tumour necrosis factor-alpha inhibitors use in four European countries,” Health Policy, vol. 104, no. 1, pp. 76–83, 2012. View at: Publisher Site | Google Scholar
  21. B. Jonsson, G. Kobelt, and J. Smolen, “The burden of rheumatoid arthritis and access to treatment: Uptake of new therapies,” European Journal of Health Economics: HEPAC: health economics in prevention and care, vol. 8, no. 8, pp. S61–S86, 2008. View at: Publisher Site | Google Scholar
  22. P. A. Laires, F. Exposto, R. Mesquita, A. P. Martins, L. Cunha-Miranda, and J. E. Fonseca, “Patients' access to biologics in rheumatoid arthritis: A comparison between Portugal and other European countries,” European Journal of Health Economics, vol. 14, no. 6, pp. 875–885, 2013. View at: Publisher Site | Google Scholar
  23. T. Sokka, H. Kautiainen, T. Pincus et al., “Disparities in rheumatoid arthritis disease activity according to gross domestic product in 25 countries in the QUEST-RA database,” Annals of the Rheumatic Diseases, vol. 68, no. 11, pp. 1666–1672, 2009. View at: Publisher Site | Google Scholar
  24. C. Y. Lu, K. M. Williams, and R. O. Day, “Access to tumour necrosis factor inhibitors for rheumatoid arthritis treatment under the australian pharmaceutical benefits scheme: are we on target?” Internal Medicine Journal, vol. 36, no. 1, pp. 19–27, 2006. View at: Publisher Site | Google Scholar
  25. E. M. Badley, M. Canizares, A. C. Gunz, and A. M. Davis, “Visits to rheumatologists for arthritis: The role of access to primary care physicians, geographic availability of rheumatologists, and socioeconomic status,” Arthritis Care & Research, vol. 67, no. 2, pp. 230–239, 2015. View at: Publisher Site | Google Scholar
  26. G. Schmajuk, C. Tonner, and J. Yazdany, “Factors associated with access to rheumatologists for Medicare patients,” Seminars in Arthritis and Rheumatism, vol. 45, no. 4, pp. 511–518, 2016. View at: Publisher Site | Google Scholar
  27. B. V. Nair, R. Schuler, S. Stewart, and R. M. Taylor-Gjevre, “Self-Reported Barriers to healthcare access for rheumatoid arthritis patients in rural and northern saskatchewan: a mixed methods study,” Musculoskeletal Care, vol. 14, no. 4, pp. 243–251, 2016. View at: Publisher Site | Google Scholar
  28. K. Souliotis, M. Papageorgiou, A. Politi, D. Ioakeimidis, and P. Sidiropoulos, “Barriers to accessing biologic treatment for rheumatoid arthritis in Greece: The unseen impact of the fiscal crisis - The Health Outcomes Patient Environment (HOPE) study,” Rheumatology International, vol. 34, no. 1, pp. 25–33, 2014. View at: Publisher Site | Google Scholar

Copyright © 2018 Cătălin Codreanu et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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