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Changes in dementia diagnoses in Sweden during the COVID-19 pandemic



The COVID-19 pandemic has caused large disruptions to healthcare systems. Refocus on COVID-19 related care might have contributed to indirect effects on other healthcare areas. Care focused on acute conditions have been negatively affected although research into the effects on chronic and care intensive patient groups such as patients with dementia diseases is lacking. In this study we evaluated dementia diagnosis trends in Sweden during 2015–2020 according to International Classification of Disease version 10 coding of common dementia diseases.


Regional and national statistics in the form of International Classification of Disease version 10 coding, COVID-19 incidence, mortality data, and population census data were collected from the National Institute of Health and Welfare. Logistic regression analysis was performed to identify trends of dementia diagnosis during 2015–2020. Correlation test was performed between COVID-19 incidence, mortality rates, and dementia coding.


Dementia diagnosis incidence has been declining since 2015 and further decline was noted in many regions in Sweden during 2020. As COVID-19 incidence increased, fewer cases of dementia were diagnosed, a decrease that differentially impacted women and those who were advanced in age.


Dementia diagnosis incidence in Sweden has been on a decline since 2015. The COVID-19 pandemic caused a further larger decline in dementia diagnosis incidence during 2020. COVID-19 incidence, but not mortality, was associated with decrease in dementia diagnosis incidence. There might be a large number of undiagnosed patients with dementia and healthcare reforms should be enacted to address this. Women and elderly are particularly vulnerable groups.

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The SARS-CoV-19 (COVID-19) pandemic has caused great disturbance to healthcare systems around the world [1, 2]. Many studies have reported lessened and worse quality of care for several acute conditions during the pandemic [3,4,5]. Changes in disease mortality trends have also been noted amongst several common diseases [6]. However, knowledge about the indirect impact of the pandemic on chronic conditions is not yet fully elucidated and the implications of healthcare disruptions amongst vulnerable groups is still an area of active research [7,8,9]. In order to formulate healthcare reforms and amend the damage caused by the pandemic, chronic and care-intensive patient groups needs to be studied in order to predict longitudinal effects.

An approximation of a specific disease burden can be obtained by studying the rate of healthcare visits per diagnosis in specialized out- and inpatient settings. The registration of specific International Statistical Classification of Diseases and Related Health Problems-Tenth revision (ICD-10) codes represents new diagnoses and follow-up visits and is indicative of the healthcare that a specific patient group receives. A decrease in ICD-10 coding therefore represents decreased care aimed towards a diagnosis. A significant disruption to care for a certain diagnosis group would be detectable in normal registry data. Vulnerable patient groups can be identified by categorizing diagnoses by age and sex. This knowledge is helpful in guiding future healthcare intervention and highlight the patient groups disproportionally affected by the pandemic.

Patients with dementia are some of the most care-intensive groups in health care systems. Diseases such as Alzheimer’s disease (AD), vascular dementia, and unspecified dementia take up large resources in the form of diagnostics and care. Physician’s visits, home care, long-term institutional care, and hospital stays for dementia patients are factors that account for a large portion of developed countries healthcare budgets [10, 11]. Despite this, dementia remains underdiagnosed [12, 13]. The increased implementation of acute care and change in clinical focus during the COVID-19 pandemic might have exacerbated the underdiagnosis of dementia and contributed to less care directed towards dementia populations. It is important to study the incidence of dementia diagnosis in specialized healthcare settings to quantify the pandemic impact on dementia patients.

In Sweden, healthcare systems rely on diagnostic coding, both in specialized out- and inpatient settings. Patient visits are coded per ICD-10 code according to the main reason for the visit. This coding includes both new diagnoses and follow up visits associated with that diagnosis. National statistics on the frequency of ICD-10 codes are available for both research and quality control purposes. Dementia diagnostics are interesting as they represent a significant healthcare burden both in both treatment and ongoing long-term patient care. Studies in other countries have shown that the COVID-19 pandemic has affected disease recognition and diagnosis, particular amongst age-associated illnesses in both primary care and hospital settings [14, 15]. The diagnosis of dementia has also been reported to have fallen drastically [14, 16, 17]. Furthermore, concerns have been raised regarding the disruption of care aimed towards noncommunicable and chronic diseases such as AD [18, 19]. The disruption to routine care for chronic health conditions will likely surpass the duration of the pandemic and have implications for years to come.

It exists no dementia incidence registry in Sweden but a quality-of-care registry, SveDem, register most new dementia diagnoses from both primary and specialist care. This data does not allow for incidence calculation but can be used to estimate if most dementia diagnosis is performed in either primary or specialist care.

There are indications of a decreasing incidence of dementia in Sweden [20, 21]. However, because of demographic trends with more elderly, the number of people with dementia is nevertheless increasing [22]. Thus, fewer dementia diagnoses as a result of the COVID-19 pandemic might lead to misrepresentation of disease burden caused by dementia, prompting research into this area.

By assessing the disease burden of dementia, measured as dementia-associated ICD-10 coding in out- and inpatient specialized care during 2020 compared to previous years, we aimed to evaluate how hard dementia diagnosis incidence were hit by the COVID-19 pandemic in Sweden. As various regions of Sweden report their ICD-10 coding separately, we furthermore aimed to study regional differences in dementia diagnosis incidence between the 21 regions of Sweden.

Materials and methods

Data acquisition

Sweden consists of 21 administrative regions; each one is responsible for healthcare within a designated geographical area. Oversight exists in the form of a central institution, the National Board of Health and Welfare, which register a multitude of data for quality assurance and research purposes. Among the parameters registered are ICD-10 codes. ICD-10 coding is used to quantify, amongst other things, the primary cause to why a patient required specialized care as well as new diagnoses. Data is reported by specialist care in both out- and inpatient settings.

We studied the reported incidence of dementia associated ICD-10 codes as described by the European shortlist of causes of death [23]. We included the ICD-10 codes for Alzheimer’s disease (G30), dementia concurrent with AD (F00), vascular dementia (F01), and unspecified dementia (F03) in the analysis. Using these codes, we collected all regional reported dementia cases reported per 100.000 inhabitants at the age of 65 or older. COVID-19 incidence, all-cause-, and dementia related mortality data per 100.000 were also retrieved from the database of the National Board of Health and Welfare. ICD-10 codes used for COVID-19 incidence included COVID-19-virus identified (U07.1) and COVID-19-virus not identified (U07.2). COVID-19 incidence was defined as number of cases per 100.000.

We collected all-cause mortality and dementia mortality. Mortality data was defined as the primary cause of death per 100.000. Dementia mortality included only deaths where the primary cause of death described on the death certificate was one of the previously described dementia codes. Data was obtained from the registers of the National Board of Health and Welfare and Statistics Sweden from 2015 to 2020 [24, 25].

We used SveDem data concerning newly registered dementia cases in primary or specialist settings from 2018 to 2020 in order to be able to compare between the two settings [26].

All data used were anonymized, publicly available and therefore not subjected to ethical review.


We used incidence of dementia diagnosis, measured as ICD-10 coding, from 2015 to 2019 to estimate the expected dementia diagnosis incidence for 2020. We deliberately chose to include only data starting at 2015 to emphasize recent trends in dementia diagnosis.

To estimate the predicted number of dementia diagnosis during 2020 we used logistic regression of the years 2015–2019 with the logarithm of dementia diagnosis as the dependent variable and the year as a continuous independent variable. The predicted number for 2020 was then calculated from the function equation and compared to actual outcome. To compare ratios of various dementia diagnosis in different settings, primary or specialist care, the same calculation was made with a logistic regression using the ratio of dementia diagnosis per setting as the dependent variable. Age cohorts were created, defined as dementia associated codes registered with people of either 65–74, 75–85, or 85+ years of age. The data was further subdivided in gender to assess sex specific differences. We analyzed the incidence for dementia diagnosis for 2020 by categorizing the data for each of the regions of Sweden in order to establish geographical differences. We used correlation analysis to determine the impact of COVID-19 incidence and mortality data on dementia diagnosis incidence. Correlation analysis was performed using Pearson correlation coefficient with a t-tailed t-test, p-value was considered significant at < 0.05. Data analysis was performed in SPSS version 28.0 (IBM, USA). All graphs were created using GraphPad version 9.1.1 (San Diego, CAL, USA).


There were significant regional differences in the incidence of dementia diagnosis when comparing expected to actual outcome. Most regions, 19 out of 21, reported a decrease in dementia diagnosis incidence during 2020 (Table 1).

Table 1 Regional differences in dementia diagnosis amongst the 21 regions in Sweden and the country as a whole. A majority of regions showed a significant decrease in dementia diagnosis

Significant differences in expected dementia diagnosis incidence could be found in 19/21 regions. National change in the incidence for dementia diagnosis during 2020 was − 20%. Urban centers and northern rural areas showed the largest changes in dementia diagnosis incidence (Supplemental Fig. 1).

Having found a significant drop in dementia diagnosis incidence during 2020, we wanted to investigate whether any patient populations were more affected than others. We therefore divided the data into age and sex groups in order to establish age or sex as a risk factor. Assessing the dementia diagnosis trends in Sweden during 2015–2019 showed no changes in dementia diagnoses for patients aged 65–74. For patient aged 74–85 or 85+, the incidence of dementia diagnosis has been slowly declining since 2015 (Fig. 1) (Supplemental Table 1).

Fig. 1
figure 1

Dementia diagnoses trends per age and sex during 2015–2020. Whole year data indicated. Dementia diagnosis incidence has been slowly declining amongst elderly since 2015 with 2020 showing a further decrease in dementia diagnosis

There was no difference in dementia diagnosis incidence amongst men and women aged 65–74. In older groups, dementia diagnosis incidence has been declining during the last 5 years. 2020 marked a significant drop for all groups. Comparison between groups showed distinct differences (Table 2). Older age and female gender were associated with decreased dementia diagnosis incidence.

Table 2 Differences in dementia diagnosis incidence amongst age and sex groups. Elderly women were noted to experience a particular large decrease in dementia diagnosis

2020 was a year of with many COVID-19 infections in Sweden and regions were hit unevenly. We correlated regional COVID-19 incidence as well as total mortality and dementia specific mortality against the incidence of dementia diagnosis to investigate whether COVID-19 infections or mortality drove dementia diagnosis decrease. Correlation analysis showed that as COVID-19 incidence increased, dementia diagnosis incidence decreased (Fig. 2). There was no correlation between all-cause mortality or dementia specific mortality (data not shown).

Fig. 2
figure 2

Regional COVID-19 incidence correlated to dementia diagnoses indicated that COVID-19 incidence caused a decline in dementia diagnoses throughout the country

The majority of ICD-10 dementia codes were AD, with vascular dementia, and unspecified dementia making up the rest. We wanted to account for shifts in dementia diagnosis groups, such as AD ICD-10 coding transferring to unspecified dementia. We therefore compared the proportion of the various ICD-10 codes that were measured between 2019 and 2020. Whole nation data showed small ratio changes for AD and unspecified dementia with vascular dementia showing a ratio change of − 9.1% indicating a change in diagnostics aimed primarily away from vascular dementia (Table 3).

Table 3 Changes in percentages of dementia sub diagnoses making up dementia patient population. Large shift towards unspecified dementia and decrease in vascular dementia is noted, indicating a possible lack of quality amongst dementia diagnostics

Pandemic conditions might cause dementia diagnoses to be allocated from specialized to primary care. No dementia incidence registry is available in Sweden although the Swedish registry for dementia, SveDem, can account for the location of dementia diagnosis, either in primary or specialist care. To account for changes in specialist versus primary care settings, the percentage of dementia diagnosis in primary care versus specialist care settings were compared. The ratio for 2020 did not differ from predicted values, indicating that a lack of diagnosis in specialist care settings could not be explained by an increase in primary care (Fig. 3).

Fig. 3
figure 3

Percentage of dementia diagnoses in specialist and primary care. Dementia diagnoses percentage remained unchanged during 2020 compared to previous years. Green symbols represent predicted values for 2020


The knowledge about the COVID-19 pandemic’s impact on chronic conditions such as dementia is lacking. The quantification of changes in dementia diagnosis incidence is essential in order to formulate future response and health reforms aimed toward the frail and elderly. In this study we compared ICD-10 dementia coding incidence in Sweden and its geographical regions in order to determine pandemic impact on dementia associated ICD-10 coding. We found a large reduction in dementia coding for the most common dementia codes throughout the country. This reduction was associated with regional COVID-19 incidence, with a higher COVID-19 incidence producing a larger decline in dementia diagnosis incidence. Elderly and women were groups that experienced disproportionally significant decreases in dementia diagnostics.

Our data showed that Swedish dementia diagnostics have been on a downwards trends the last few years, particular amongst elderly patient groups. This downward trend was exacerbated during the 2020 pandemic and resulted in a further decline in dementia diagnoses. Lack of knowledge regarding diagnosis criteria, refocus on other chronic conditions, and underfunded primary care system might be factors that contributed to this outcome. The need for dementia diagnosis is crucial and further highlighted by the COVID-19 pandemic. Patients with cognitive impairments are vulnerable to social isolation and decreases in mental stimulation. Isolation and decreased mental stimuli are both risk factors for dementia that have increased during the pandemic and directly lead to deterioration in cognitive function and increase the risk of dementia [27, 28].

Women and elderly in particular are at risk of dementia and represent vulnerable patient groups [29, 30]. This was also noted in our study with women and elderly patient groups having larger decreases in dementia diagnosis incidence when compared to other groups. It also appears that there are different levels of tolerance towards disruptions in diagnostics amongst the various diagnosis groups of dementia as we found vascular dementia cases to be more reduced compared to AD and unspecified dementia.

As ICD-10 coding does not differ between new diagnoses and follow up care, only expected incidence can be calculated. However, it is likely that both new diagnoses and follow up care are affected. This means that there is a significant underdiagnosis of dementia occurring in conjunction with the COVID-19 pandemic. This could mean that a large patient population is undiagnosed and left outside of the healthcare that they need, as patients with dementia are often dependent on services and special care. We suggest that healthcare systems should take actions to mitigate this shortcoming by allocating resources to primary care and geriatric clinics in order increase screening and diagnosis of new dementia cases. Decrease in registered dementia cases during 2020 might have been mitigated by the implementation of remotely accessible consultations, so called telemedicine, a strategy that has been applied in other countries [31,32,33].

The incidence of COVID-19 might skew statistics. As elderly are more susceptible to severe infection, a decrease in the total number of patients due to mortality might explain a decrease in dementia diagnosis incidence. We controlled for regional COVID-19 incidence and mortality, both all-cause and dementia. We found correlation between COVID-19 incidence and decrease in dementia diagnosis incidence. Regions with high COVID-19 incidence displayed larger decreases in dementia diagnosis. This is not surprising, given that a rerouting of resources and healthcare workers from a non-acute healthcare section to an acute one is to be expected. However, there was no correlation between mortality and dementia diagnosis incidence indicating that an increased mortality is not the cause of a decrease in dementia. This decrease is more likely driven by the overall healthcare burden on regional systems. If so, a continued dysfunction of dementia diagnosis can be expected for as long as the pandemic continues.

One further explanation for a decrease in dementia diagnosis incidence in specialist care could be an increase in primary care. This would occur as patients are being treated in primary care settings rather than being referred to specialist care. To account for this, we compared percentage of registered dementia diagnosis in primary versus specialist settings in a quality-of-care registry showing no significant change. This indicates that the lack of dementia care in specialist settings is not compensated by an increase in primary care. Together, these findings suggest that there are likely many undiagnosed and under-treated dementia patients in Sweden in the wake of the pandemic.

The results of this study are not surprising given that the COVID-19 pandemic and its subsequent restrictions has limited mobility of the elderly, likely leading to fewer doctor’s visits. Similar studies and reports in other countries have found results that are in line with our findings, showing large decreases in dementia diagnoses [14, 16, 17, 34]. Our study adds Sweden to the countries in which dementia diagnoses have been severely affected by the COVID-19 pandemic. If COVID-19 incidence is the driving factor behind decreased dementia diagnostics, then this pandemic might have worldwide ramifications for dementia patients and their caretakers.

Elderly patients are vulnerable to COVID-19 infections. Recommendations to stay at home and an unwillingness to expose oneself to hospital settings might be further contributing factors to decreased dementia diagnoses. Healthcare reprioritization in the form of relocation of healthcare resources from memory clinics and primary care centers is also likely to contribute to decrease in dementia diagnostics and treatments.

Due to the difficult and time-consuming process associated with confirming a dementia diagnosis, the drop in dementia diagnosis incidence might represent a significant loss in knowledge and experience amongst physicians treating dementia patients. Such a knowledge gap can prove disastrous going forward as the incidence of dementia might continue to decrease, leaving more and more patients without adequate care.


There are some weaknesses inherent with the data used in this study as it excludes private caregivers and does not differ between new diagnoses and follow-up visits. The data is assumed to be accumulative as more physicians are made aware of the registry as time goes on, making it difficult to draw conclusions about increases in dementia diagnosis incidence across regions. We were also unable to compare incidence of dementia in primary versus specialist care as such a dementia incidence registry does not exist in Sweden. Neither have we included data from the municipality sector, who has the main responsibility for long term care and home services.


COVID-19 is correlated to decreases in dementia diagnoses as measured by ICD-10 coding. Elderly and women were particularly impacted with large decreases in dementia diagnosis incidence when compared to other groups. There is no evidence that a shift from specialist to primary care account for the lack of dementia diagnostics, indicating a large number of untreated and undiagnosed patients. Healthcare systems should carefully consider this lack of dementia diagnosis going forward.

Availability of data and materials

All data is available from the authors on request. Primary ICD-10 coding data is freely available from the public records of the National Board of Health and Welfare. SveDem data is available from the SveDem website.


  1. Barach P, Fisher SD, Adams MJ, Burstein GR, Brophy PD, Kuo DZ, et al. Disruption of healthcare: will the COVID pandemic worsen non-COVID outcomes and disease outbreaks? Prog Pediatr Cardiol. 2020;59:101254.

    Article  Google Scholar 

  2. Blumenthal D, Fowler EJ, Abrams M, Collins SR. Covid-19 - implications for the health care system. N Engl J Med. 2020;383(15):1483–8.

    CAS  Article  Google Scholar 

  3. Rinkel LA, Prick JCM, Slot RER, Sombroek NMA, Burggraaff J, Groot AE, et al. Impact of the COVID-19 outbreak on acute stroke care. J Neurol. 2021;268(2):403–8.

    CAS  Article  Google Scholar 

  4. Mohseni M, Ahmadi S, Azami-Aghdash S, Mousavi Isfahani H, Moosavi A, Fardid M, et al. Challenges of routine diabetes care during COVID-19 era: a systematic search and narrative review. Prim Care Diabetes. 2021;S1751-9918(21):00134–0.

    Google Scholar 

  5. Fersia O, Bryant S, Nicholson R, McMeeken K, Brown C, Donaldson B, et al. The impact of the COVID-19 pandemic on cardiology services. Open Heart. 2020;7(2):e001359.

    Article  Google Scholar 

  6. Axenhus M, Schedin-Weiss S, Winblad B, Wimo A. Changes in mortality trends amongst common diseases during the COVID-19 pandemic in Sweden. Scand J Public Health. 2021:14034948211064656.

  7. Alyammahi SK, Abdin SM, Alhamad DW, Elgendy SM, Altell AT, Omar HA. The dynamic association between COVID-19 and chronic disorders: an updated insight into prevalence, mechanisms and therapeutic modalities. Infect Genet Evol. 2021;87:104647.

    CAS  Article  Google Scholar 

  8. Chudasama YV, Gillies CL, Zaccardi F, Coles B, Davies MJ, Seidu S, et al. Impact of COVID-19 on routine care for chronic diseases: a global survey of views from healthcare professionals. Diabetes Metab Syndr. 2020;14(5):965–7.

    Article  Google Scholar 

  9. Singh K, Kaushik A, Johnson L, Jaganathan S, Jarhyan P, Deepa M, et al. Patient experiences and perceptions of chronic disease care during the COVID-19 pandemic in India: a qualitative study. BMJ Open. 2021;11(6):e048926.

    Article  Google Scholar 

  10. Wimo A, Guerchet M, Ali G-C, Wu Y-T, Prina AM, Winblad B, et al. The worldwide costs of dementia 2015 and comparisons with 2010. Alzheimers Dement. 2017;13(1):1–7.

    Article  Google Scholar 

  11. Cantarero-Prieto D, Leon PL, Blazquez-Fernandez C, Juan PS, Cobo CS. The economic cost of dementia: a systematic review. Dementia (London). 2020;19(8):2637–57.

    Article  Google Scholar 

  12. Amjad H, Roth DL, Sheehan OC, Lyketsos CG, Wolff JL, Samus QM. Underdiagnosis of dementia: an observational study of patterns in diagnosis and awareness in US older adults. J Gen Intern Med. 2018;33(7):1131–8.

    Article  Google Scholar 

  13. Bradford A, Kunik ME, Schulz P, Williams SP, Singh H. Missed and delayed diagnosis of dementia in primary care: prevalence and contributing factors. Alzheimer Dis Assoc Disord. 2009;23(4):306–14.

    Article  Google Scholar 

  14. Michalowsky B, Hoffmann W, Bohlken J, Kostev K. Effect of the COVID-19 lockdown on disease recognition and utilisation of healthcare services in the older population in Germany: a cross-sectional study. Age Ageing. 2021;50(2):317–25.

    Article  Google Scholar 

  15. Williams R, Jenkins DA, Ashcroft DM, Brown B, Campbell S, Carr MJ, et al. Diagnosis of physical and mental health conditions in primary care during the COVID-19 pandemic: a retrospective cohort study. Lancet Public Health. 2020;5(10):e543–50.

    Article  Google Scholar 

  16. Borson S, Chen A, Wang SE, Nguyen HQ. Patterns of incident dementia codes during the COVID −19 pandemic at an integrated healthcare system. J Am Geriatr Soc. 2021;jgs:17527.

    Google Scholar 

  17. Dementia diagnosis rates drop during pandemic | Alzheimer’s Society [Internet]. [cited 2022 Feb 21]. Available from:

  18. Kendzerska T, Zhu DT, Gershon AS, Edwards JD, Peixoto C, Robillard R, et al. The effects of the health system response to the COVID-19 pandemic on chronic disease management: a narrative review. Risk Manag Healthc Policy. 2021;14:575–84.

    Article  Google Scholar 

  19. Brown EE, Kumar S, Rajji TK, Pollock BG, Mulsant BH. Anticipating and mitigating the impact of the COVID-19 pandemic on Alzheimer’s disease and related dementias. Am J Geriatr Psychiatry. 2020;28(7):712–21.

    Article  Google Scholar 

  20. Ding M, Qiu C, Rizzuto D, Grande G, Fratiglioni L. Tracing temporal trends in dementia incidence over 25 years in Central Stockholm. Sweden Alzheimers Dement. 2020;16(5):770–8.

    Article  Google Scholar 

  21. Seblova D, Quiroga ML, Fors S, Johnell K, Lövdén M, de Leon AP, et al. Thirty-year trends in dementia: a nationwide population study of Swedish inpatient records. Clin Epidemiol. 2018;10:1679–93.

    Article  Google Scholar 

  22. snacsweden. Ny rapport! Demensförekomst i Sverige: geografiska och tidsmässiga trender 2001–2013 [Internet]. SNAC. 2018 [cited 2021 Dec 8]. Available from:

  23. European Shortlist for Causes of Death | Joinup [Internet]. [cited 2021 Oct 10]. Available from:

  24. Dödsorsaksregistret [Internet]. Socialstyrelsen. [cited 2021 Dec 7]. Available from:

  25. Finding statistics [Internet]. Statistiska Centralbyrån. [cited 2021 Dec 7]. Available from:

  26. Start - SveDem [Internet]. [cited 2021 Nov 29]. Available from:

  27. Chen Z-C, Liu S, Gan J, Ma L, Du X, Zhu H, et al. The impact of the COVID-19 pandemic and lockdown on mild cognitive impairment, Alzheimer’s disease and dementia with Lewy bodies in China: a 1-year follow-up study. Front Psychiatry. 2021;12:711658.

    Article  Google Scholar 

  28. Barguilla A, Fernández-Lebrero A, Estragués-Gázquez I, García-Escobar G, Navalpotro-Gómez I, Manero RM, et al. Effects of COVID-19 pandemic confinement in patients with cognitive impairment. Front Neurol. 2020;11:1555.

    Article  Google Scholar 

  29. Beam CR, Kaneshiro C, Jang JY, Reynolds CA, Pedersen NL, Gatz M. Differences between women and men in incidence rates of dementia and Alzheimer’s disease. J Alzheimers Dis. 2018;64(4):1077–83.

    Article  Google Scholar 

  30. van der Flier WM, Scheltens P. Epidemiology and risk factors of dementia. J Neurol Neurosurg Psychiatry. 2005;76(suppl 5):v2–7.

    Article  Google Scholar 

  31. Lian X, Dalan R, Seow CJ, Liew H, Jong M, Chew D, et al. Diabetes care during COVID-19 pandemic in Singapore using a telehealth strategy. Horm Metab Res. 2021;53(3):191–6.

    CAS  Article  Google Scholar 

  32. Garcia-Huidobro D, Rivera S, Valderrama Chang S, Bravo P, Capurro D. System-wide accelerated implementation of telemedicine in response to COVID-19: mixed methods evaluation. J Med Internet Res. 2020;22(10):e22146.

    Article  Google Scholar 

  33. Ramaswamy A, Yu M, Drangsholt S, Ng E, Culligan PJ, Schlegel PN, et al. Patient satisfaction with telemedicine during the COVID-19 pandemic: retrospective cohort study. J Med Internet Res. 2020;22(9):e20786.

    Article  Google Scholar 

  34. Recorded Dementia Diagnoses [Internet]. NHS Digital. [cited 2022 Feb 22]. Available from:

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We acknowledge the National board of Health and Welfare for offering their data for public analysis, without which, this study would be impossible.


Open access funding provided by Karolinska Institute.

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MA and BW conceptualized the study and obtained the data. AW contributed statistical oversight. MA performed the formal analysis. MA, SSW, GB developed the methodology. SSW, LT supervised the project. All authors reviewed and contributed to the drafting of the manuscript. All authors have read and approved the manuscript.

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Correspondence to Michael Axenhus.

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Supplementary Information

Additional file 1: Supplementary Fig. 1.

Regional dementia coding in Sweden during 2020 compared to expected value. The largest decreases in the number of dementia diagnoses could be found in densely populated urban areas and northern rural areas.

Additional file 2: Supplementary Table 1.

Dementia diagnoses per age and sex group during 2015–2020. A decline in dementia diagnoses can be detected in most groups even before the COVID-19 pandemic.

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Axenhus, M., Schedin-Weiss, S., Tjernberg, L. et al. Changes in dementia diagnoses in Sweden during the COVID-19 pandemic. BMC Geriatr 22, 365 (2022).

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  • Alzheimer’s disease
  • COVID-19
  • Dementia
  • Diagnosis
  • Sweden
  • Vascular dementia