Skip to main content
Advertisement
Browse Subject Areas
?

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

  • Loading metrics

Representation of Parkinson's disease and atypical Parkinson's syndromes in the Czech Republic—A nationwide retrospective study

  • Jiří Búřil ,

    Contributed equally to this work with: Jiří Búřil, Petra Búřilová

    Roles Conceptualization, Methodology, Validation, Writing – original draft, Writing – review & editing

    Jirka210312@gmail.com

    Current address: Ist Department of Neurology, St. Anne´s University Hospital, Brno, Czech Republic

    Affiliation Ist Department of Neurology, Faculty of Medicine, Masaryk University, Brno, Czech Republic

  • Petra Búřilová ,

    Contributed equally to this work with: Jiří Búřil, Petra Búřilová

    Roles Conceptualization, Data curation, Methodology, Validation, Visualization

    Affiliations Department of Nursing and Midwifery, Faculty of Medicine, Masaryk University, Brno, Czech Republic, The Institute of Health Information and Statistics of the Czech Republic, Prague, Czech Republic

  • Andrea Pokorná ,

    Roles Conceptualization, Data curation, Supervision, Validation, Writing – review & editing

    ‡ These authors also contributed equally to this work.

    Affiliations Department of Nursing and Midwifery, Faculty of Medicine, Masaryk University, Brno, Czech Republic, The Institute of Health Information and Statistics of the Czech Republic, Prague, Czech Republic

  • Ingrid Kováčová,

    Roles Conceptualization, Data curation, Formal analysis

    Affiliation The Institute of Health Information and Statistics of the Czech Republic, Prague, Czech Republic

  • Marek Baláž

    Roles Conceptualization, Supervision, Writing – review & editing

    Current address: Ist Department of Neurology, St. Anne´s University Hospital, Brno, Czech Republic

    ‡ These authors also contributed equally to this work.

    Affiliation Ist Department of Neurology, Faculty of Medicine, Masaryk University, Brno, Czech Republic

Abstract

Background

Parkinson's disease is a progressive neurodegenerative disease which causes health problem that affects more patients in the past few years. To be able to offer appropriate care, epidemiological analyses are crucial at the national level and its comparison with the international situation.

Aim

The demographic description of reported patients with parkinsonism (including Parkinson's disease and atypical parkinsonian syndromes) according to the International Classification of Diseases (ICD-10) from the national health registries.

Methods

Retrospective analysis of data available from the National Health Information System–NHIS and the National Registry of Reimbursed Health Services (NRRHS). Analyzed epidemiological data are intending to determine the regional and specific prevalence of Parkinsonism in the Czech Republic. The International Classification of Diseases diagnoses (ICD-10) of G20 (Parkinson’s disease—PD) and G23.1, G23.2, G23.3 (other degenerative disorders of basal ganglia), and G31.8 (another degenerative disease of basal ganglia) from the period of 2012 to 2018 were included into the analysis.

Results

We identified 78 453 unique patients from national registries in the period 2012 to 2018. Diagnoses of G20, G23.1, G23.2, and G31.8 were registered as the principal diagnoses in 76.6% of all individual patients.

Conclusion

We have found a growing number of patients coded with ICD-10 of dg. G20, G23.1, G23.2, G23.3, or G31.8 (N = 27 891 in 2012, and N = 30 612 in 2018). We have proven regional differences in the prevalence of Parkinson´s diagnoses. Therefore we assume most likely also differences in the care of patients with PD based on the availability of specialty care centers.

Introduction

Parkinson's disease (PD) is a progressive neurodegenerative disease that affects mainly the function of basal ganglia. Common PD motor signs include bradykinesia, rigidity, tremor, and postural instability. Incidence and prevalence of PD appear to increase over the recent years [1]. PD signs tend to progress over the period of several years from early non-motor symptoms to fully developed parkinsonian syndrome as described by Braak pathological stages [2]. Motor signs, e.g., parkinsonian syndrome, can be controlled by dopaminergic treatment, especially in the early stages of the disease. Advanced stage of PD—accompanied by late/advanced motor symptoms and fluctuations of motor state—usually occurs within 5 to 7 years since the onset of the disease [3]. Therapeutic options become more complex with the advancing PD stage [4].

The prevalence of the disease ranges from 1 to 3 per 1000 in unselected populations, and it affects 1% of the population above 60 years [5]. According to a recent study, methodological differences between studies make a direct comparison of prevalence estimates difficult [6, 7]. Global Burden of Disease study points to estimates of approximately 13 million people treated for PD by 2040 [8]. Last available data from IHIS CR (Institute for Health Information and Statistics of the Czech Republic–

Ústav zdravotnických informací a statistiky České republiky) from 2012 report 26 680 patients [9]. The population of the Czech Republic in 2012 reached approximately 10 516 000 people. The prevalence at that time point was 2.53 per 1000 inhabitants. Young-onset PD patients with diagnosis established before the age of 40, comprised 15% [10]. Other papers have reported different prevalence of data [11, 12]. Available data show the average age of PD diagnosis between 50 and 60 years. Therefore, it is clear that the disease affects people of productive age. PD prevalence grows with increasing age, and it will further increase due to an increase in longevity. We decided to perform a retrospective analysis of national health statistic data to elucidate a number of patients treated for PD in the Czech Republic as we are aware that the valid data on prevalence may be necessary for both healthcare providers and health and social care payers, as well as for patient groups.

Aim of the analyses

The demographic description of reported patients with parkinsonism (including Parkinson's disease and atypical parkinsonian syndromes) according to the International Classification of Diseases (ICD-10) from the national health registries.

Materials and methods

We performed a retrospective analysis of data available from NHIS (National Health Information System), respectively NRRHS (National Registry of Reimbursed Health Services) with respect to the STROND checklist. In both registries, the data from health care providers about the type and amount of care are collected. We analyzed epidemiological data intending to determine the regional and specific prevalence of Parkinsonism in the Czech Republic. The International Classification of Diseases (ICD-10) diagnoses of G20 (Parkinson’s disease) and G23.1, G23.2, G23.3 (other degenerative disorders of basal ganglia), and G31.8 (another degenerative disease of basal ganglia) from the period of 2012 to 2018 were included into the analysis. Atypical parkinsonian syndromes were included due to overlap of clinical signs, at least during the initial stages of Parkinsonism. We selected the period till 2018, as the last previous data on national prevalence were published in 2018. The diagnosis G23.3 (according to ICD-10) was not found in the analyzed data, so we excluded this diagnose from our further evaluation. The standardized annual prevalence of the patients with parkinsonism (including Parkinson's disease and atypical parkinsonian syndromes) has been counted. The analyzes of age and gender distribution, age in the date of diagnosis, and regional distribution of patients within the Czech Republic districts in the analyzed sample.

Patient and public involvement

No patients were involved in the design of the study. For the research purposes analyses, there is not special ethical approval needed according to the Czech law if they are analyzing by the Institute of Health Information and Statistics and not by the third party.

Results

We identified 205 490 records of patients with PD from national registries in the period from 2012 to 2018 (averaging 29 000 patients per year, Fig 1), which means 78 453 unique patients in total (each patient could be recorded just one time during the year, but several times during the whole period from 2012 to 2018). We have found a growing number of records coded with ICD-10 of dg. G20, G23.1, G23.2, or G31.8 (N = 27 891 in 2012, and N = 30 612 in 2018). The diagnosis G23.3 (according to ICD-10) was not found in the analyzed data, so we excluded this diagnose from our further evaluation. Diagnoses of G20, G23.1, G23.2, a G31.8 (International Classification of Diseases–ICD-10) were registered as the principal diagnoses in 76.6% of all individual patients. After extrapolation to the overall population, a standardized annual prevalence reached 276 per 100 000 inhabitants. After the age and gender distribution was taken into account, a higher incidence was found in the age group of over 65 years, 48% of patients were men, 52% women. The average patient age was lower in males (73 years) than female patients (75 years) (Fig 2). Most frequent age at diagnosis (i.e., age at which a diagnosis was registered with diagnosis in the health care system) was in the range of 75–79 years. We determined the number of patients with these diagnoses concerning regional distribution within districts of the Czech Republic (Fig 3).

thumbnail
Fig 1. Number of records patients with diagnosis G20, G23.1, G23.2 or G31.8 in individual years.

https://doi.org/10.1371/journal.pone.0246342.g001

thumbnail
Fig 2. Demographic profile of persons with diagnosis G20, G23.1, G23.2 or G31.8.

https://doi.org/10.1371/journal.pone.0246342.g002

thumbnail
Fig 3. Number of patients with diagnosis G20, G23.1, G23.2 or G31.8 by residence in relation to the population of the region in the Czech Republic.

https://doi.org/10.1371/journal.pone.0246342.g003

Discussion

Based on the results of our analysis, we identified approximately 29 000 records of patients per year treated for Parkinsonism in the Czech Republic. Only 4.2% (from the whole period 2012–2018) of these patients were followed under ICD-10 diagnostic codes of atypical Parkinsonism (G23.1, G23.2, G23.3, G31.8). According to available published data, the reported prevalence of atypical Parkinsonism is 0.4% (400 cases per 100 000 populations) in dementia with Lewy bodies (G31.8), multisystem atrophy with dominant parkinsonian features (MSA-P, G23.2), and progressive supranuclear palsy (PSP, G23.1) in 5 to 10 cases per 100 000 of the general population, increasing to 7 to 8 per 100 000 inhabitants in elderly [13]. The ratio of the parkinsonian subtype of MSA to the cerebellar subtype is 2:1 to 4:1 in 66 countries [14, 15]. Diagnosis code G23.3 of multiple system atrophy—cerebellar type (a rare disorder with an estimated average prevalence of 0.6 to 0.7 per 100 000 inhabitants [16]) was not present in the Czech national health registries. The possible reason is, that there were no incidence of patients with dg. G23.3 which could relate to the problem that the clinicians are unable to diagnose it appropriately. Also published literature is confirming that the dg. G23.3 is not reported, the commonly used codes are 23.1, 23.2 and 23.9 [17]. Another possibility is that the clinicians do not show dg. multisystem atrophies correctly under the code G 23.3, but under the general one, for example G31.8. Our analysis has shown an average prevalence of 9.8 per 100 000 of code G31.8, 1.2 per 100 000 of code G23.1, and 0.7 per 100 000 of code G23.2 (from the whole period 2012–2018). We did not report cases of corticobasal degeneration. Those are reserved for the neuropathological diagnosis. However, it can be estimated that at least a certain share of patients coded as G20 (PD) was, in fact, patients with atypical parkinsonian syndromes. Therefore, atypical parkinsonian syndromes may be underdiagnosed. However, they should not be underestimated in the differential diagnosis of Parkinsonism [13].

According to data available from health registries (NHIS), we have shown that most patients diagnosed and treated with PD were in the age group of 70–84 years (50.3% male and 49.7% women). Age at the time of PD diagnosis was 70–84 years, which differs from available EU data [16, 18]. European data sets show age at the time of diagnosis lower by 10–15 years. We speculate that inadequate diagnosis or late registering of a patient under the correct ICD code may be the cause of a later diagnosis age, found at our registries. We cannot assume that the diagnosis and treatment of a patient with Parkinsonism occur late. Diagnostic accuracy may differ concerning disease duration (lower during the first contact of a patient with early parkinsonian symptoms), age of a patient (possibility of later diagnosis in younger patients), the experience of a physician, and understanding of PD. Diagnostic mistakes may be caused by overlapping symptoms in the early stages of Parkinsonism and the similarity of other disorders (essential tremor, dystonic tremor). The current diagnosis of PD is aided by established clinical diagnostic criteria [19, 20]. Some patients may lack early access to a neurologist specialized in movement disorders, perhaps also due to the uneven geographic distribution of centers focused on movement disorders. There are two centers in the eastern part of the country—(Moravia and Silesia with almost 5 million inhabitants) and a single center in the western part (Bohemia, with approximately 5.5 million inhabitants). Another possible cause of potentially late diagnosis may be due to limited healthcare awareness and underestimation of disease signs, as was shown in 59.4% of the Czech population by a survey related to the preparation of the program “Health 2020” in the Czech Republic [21]. Various genetic and social factors may influence the regional distribution of patients with Parkinsonism, as was already reported in the eastern part of our country [22]. We did not have the possibility to deeper analysed the data about recorded patients (gender and age) and because of this we have look at the records based on the place where the care was provided. The highest rate of PD diagnosis was found in districts of Zlin Region (386 cases per 100 000 inhabitants), Vysočina Region (346 cases per 100 000 inhabitants), and Olomouc Region (319 cases per 100 000 inhabitants). The exact location of the residence was not possible to determine in 247 cases analyzed for 2018.

We are aware of several limitations of this study. Both unintentional and intentional coder errors, such as misspecification, and up-coding, as potential sources of errors, were described [23]. As we have limited knowledge about the exact diagnostic coding by individual physicians and in various hospitals over the country, we cannot determine the level of coding mistakes that may have occurred, similarly as was reported in a recent study on diagnostic accuracy in Parkinsonism [24, 25].

The importance of the availability of movement disorder centers is underscored by data showing that nearly half (47%) of PD diagnoses are incorrect when performed in the primary care setting. Specialists without expertise in movement disorders have an error rate of approximately 25%, while movement disorder specialists made mistakes in only 6% to 8% of cases [26, 27].

Conclusion

According to available epidemiological data from the Czech health care registries, we were able to perform an analysis of population data concerning ICD-10 codes coding Parkinsonism and related disorders. We also analyzed the regional prevalence of these diagnoses in respective regions of the Czech Republic. We have found a growing number of records coded with ICD-10 of dg. G20, G23.1, G23.2, G23.3, or G31.8 (N = 27 891 in 2012, and N = 30 612 in 2018). We have proven regional differences in the prevalence of diagnoses. Therefore we assume most likely also differences in the care of patients with PD based on the availability of specialty care centers. The big issue for the future in the Czech Republic is the implementation of the standardized processes of care based on nationally accepted evidence-based guidelines.

References

  1. 1. Pringsheim T, Jette N, Frolkis A, Steeves TD. The prevalence of Parkinson's disease: a systematic review and meta-analysis. Mov Disord. 2014; 29:1583–1590. pmid:24976103
  2. 2. Braak H, Del Tredici K, Rüb U, de Vos RA, Jansen Steur EN, Braak E. Staging of brain pathology related to sporadic Parkinson’s disease. Neurobiol Aging. 2003; 24(2):197–211. pmid:12498954
  3. 3. Isotalo J, Vahlberg T, Kaasinen V. Unchanged long-term rural-to-urban incidence ratio of Parkinson's disease. Mov Disord. 2017; 32(3):474–475. pmid:27862325
  4. 4. Ruzicka E, Roth J, Kanovsky P. Parkinsonova nemoc a parkinsonské syndromy [in Czech language] [in English language: Parkinson disease and Parkinson's syndromes]. Galén: Praha 2000. p. 98–101.
  5. 5. Tysnes O, Storstein A. Epidemiology of Parkinson’s disease. J Neural Transm. 2017; 124:901–905. pmid:28150045
  6. 6. von Campenhausen S, Bornschein B, Wick R, Bötzel K, Sampaio C, Poewe W, et al. Prevalence and incidence of Parkinson’s disease in Europe. Eur Neuropsychopharmacol. 2005; 15(4):473–490. pmid:15963700
  7. 7. de Lau LM, Breteler MM. Epidemiology of Parkinson’s disease. Lancet Neurol. 2006; 5(6):525–535. pmid:16713924
  8. 8. GBD. Parkinson’s DiseaseCollaborators. Global, regional, and national burden of Parkinson's disease, 1990–2016: a systematic analysis for the Global Burden of Disease Study. Lancet Neurol. 2018; 17:939–53. pmid:30287051
  9. 9. Team of authors. Parkinsonova nemoc z různých pohledů. [in Czech language] [in English language: Parkinson disease from different perspectives]. Company of Parkinson, o. s., Praha, 2013. [cited 2020 Aug 4]. Available from: http://www.edukafarm.cz/c1421-parkinsonova-nemoc-v-cr-aktualni-pruzkum
  10. 10. Team of authors. Epidemiologická analýza–Parkinsonova nemoc. [in Czech language] [in English language: Epidemiology analyses–Parkinson disease]. The Institute of Health Information and Statistics of the Czech Republic, 2012. [cited 2020 Aug 16]. Available from: http://www.edukafarm.cz/c1421-parkinsonova-nemoc-v-cr-aktualni-pruzkum
  11. 11. Kis B, Schrag A, Ben-Shlomo Y. Novel three-stage ascertainment method Prevalence of PD and Parkinsonism in South Tyrol, Italy. Neurology. 2002; 58:1820–1825. pmid:12084883
  12. 12. de Rijk MC, Launer LJ, Berger K, Breteler MM, Dartigues JF, Baldereschi M, et al. Prevalence of Parkinson's disease in Europe: a collaborative study of population‐based cohorts. Neurologic Diseases in the Elderly Research Group. Neurology. 2000; 54(11Suppl 5):S21–3. pmid:10854357
  13. 13. Levin J, Kurz A, Arzberger T, Giese A, Höglinger GU. The Differential Diagnosis and Treatment of Atypical Parkinsonism. Dtsch Arztebl Int. 2016; 113(5):61–9. pmid:26900156
  14. 14. Köllensperger M, Geser F, Ndayisaba JP, Boesch S, Seppi K, Ostergaard K, et al. Presentation, diagnosis, and management of multiple system atrophy in Europe: final analysis of the European multiple system atrophy registry. Mov Disord. 2010; 25:2604–2612. pmid:20922810
  15. 15. Gilman S, May SJ, Shults CW, Tanner CM, Kukull W, Lee VM, et al. The North American Multiple System Atrophy Study Group. J Neural Transm. 2005; 112:1687–1694. pmid:16284910
  16. 16. Alessandra F, Wenning GK. Multiple-System Atrophy. N Engl J Med. 2015; 372:249–263. pmid:25587949
  17. 17. Harding Z, Wilkinson T, Stevenson A, Horrocks S, Ly A, Schnier CH et al. Identifying Parkinson's disease and parkinsonism cases using routinely collected healthcare data: A systematic review. PLoS ONE. 2019; 14(1):e0198736. pmid:30703084
  18. 18. Moisan F, Kab S, Mohamed F, Canonico M, Le Guern M, Quintin C, et al. Parkinson disease male-to-female ratios increase with age: French nationwide study and meta-analysis. J Neurol Neurosurg Psychiatry. 2016; 87(9):952–7. pmid:26701996
  19. 19. Darweesh SK, Koudstaal PJ, Stricker BH, Hofman A, Ikram MA. Trends in the Incidence of Parkinson Disease in the General Population: The Rotterdam Study. Am J Epidemiol. 2016; 183:1018–1026. pmid:27188952
  20. 20. Postuma RB, Berg D, Stern M, Poewe W, Olanow CW, Oertel W, et al. MDS clinical diagnostic criteria for Parkinson's disease. Mov Disord. 2015; 30:1591–1601. pmid:26474316
  21. 21. Kucera Z, Pelikan J, Steflova A. Zdravotní gramotnost obyvatel ČR − výsledky komparativního reprezentativního šetření. [in Czech language] [in English language: Health literacy of the population of the Czech Republic—results of a comparative representative survey]. Čas. Lék. Čes. 2016; 155:233–241.
  22. 22. O’Malley KJ, Cook KF, Price MD, Wildes KR, Hurdle JF, Ashton CM. Measuring diagnoses: ICD code accuracy. Health Serv Res. 2005; 40(5 Pt 2):1620–1639. pmid:16178999
  23. 23. Mensikova K, Kanovsky P, Kaiserova M, Mikulicova L, Vastik M, Hlustik P, et al. Prevalence of neurodegenerative Parkinsonism in an isolated population in south-eastern Moravia, Czech Republic. Eur J Epidemiol. 2013; 28:833–6. pmid:23887882
  24. 24. Hustad E, Skogholt AH, Hveem K, Aasly JO. The accuracy of the clinical diagnosis of Parkinson disease. The HUNT study. J Neurol. 2018; 265(9):2120–2124. pmid:29992351
  25. 25. Wanneveich M, Moisan F, Jacqmin-Gadda H, Elbaz A, Joly P. Projections of prevalence, lifetime risk and life expectancy of Parkinson disease (2010–2030) in France. Mov Disord. 2018; 33(9):1449–1455. pmid:30145805
  26. 26. Pagan FL. Improving Outcomes Through Early Diagnosis of Parkinson's Disease. Am J Manag Care. 2012; 18:S176–S182. pmid:23039866
  27. 27. National Collaborating Centre for Chronic Conditions. Parkinson’s disease: national clinical guideline for diagnosis and management in primary and secondary care. London: Royal College of Physicians; 2006.