Skip to main content
Age and Ageing logoLink to Age and Ageing
. 2016 Dec 5;46(3):393–400. doi: 10.1093/ageing/afw208

Inequalities in receipt of mental and physical healthcare in people with dementia in the UK

Claudia Cooper 1,*, Rebecca Lodwick 2, Kate Walters 2, Rosalind Raine 3, Jill Manthorpe 4, Steve Iliffe 5,6, Irene Petersen 2
PMCID: PMC5378291  PMID: 27916749

Abstract

Background

UK Dementia Strategies prioritise fair access to mental and physical healthcare. We investigated whether there are inequalities by deprivation or gender in healthcare received by people with dementia, and compared healthcare received by people with and without dementia.

Methods

we investigated primary care records of 68,061 community dwelling dementia patients and 259,337 people without dementia (2002–13). We tested hypotheses that people with dementia from more deprived areas, and who are women receive more psychotropic medication, fewer surgery consultations, are less likely to receive annual blood pressure, weight monitoring and an annual review, compared with those from less deprived areas and men.

Results

only half of people with dementia received a documented annual review. Deprivation was not associated with healthcare received. Compared to men with dementia, women with dementia had lower rates of surgery consultations (adjusted incidence rate ratio (IRR) 0.90, 95% CI 0.90–0.91), of annual blood pressure monitoring (adjusted IRR 0.96, 95% CI 0.95–0.97) and of annual weight monitoring (adjusted IRR 0.91, 95% CI 0.90–0.93). Men with dementia were less likely to be taking psychotropic medication than women with dementia. People with dementia had fewer surgery consultations and were less likely to have their weight and blood pressure monitored at least annually, compared to the non-dementia group.

Conclusions

people with dementia, in particular women, appear to receive less primary healthcare, but take more psychotropic medication that may negatively impact their physical health. Reducing these inequalities and improving access of people with dementia to preventative healthcare could improve the health of people with dementia.

Keywords: dementia, healthcare disparities, deprivation, psychotropic drugs, equalities, medication, older people

Introduction

People with dementia have high rates of physical ill-health, most commonly hypertension and diabetes [1] and of neuropsychiatric symptoms, that may be treated with psychotropic medication, including antipsychotics [24]. Mental and physical well-being are key determinants of life quality and independent living in dementia [5]. Improving physical health may slow cognitive decline, by reducing cardiovascular pathology or functional impairment and improving diabetic control [6].

In dementia, antipsychotic prescribing is associated with cognitive decline [7], mortality [8], side effects, somnolence and falls [9] and hypnotics and anxiolytics with cognitive decline [10, 11] and falls [9]. In 2009, the UK Medicines and Healthcare products Regulatory Agency (MHRA) highlighted risks of stroke and death with antipsychotics [12], and a UK government-commissioned review prioritised reducing their use in dementia [13]; UK usage has fallen since these publications [1416].

People with dementia may be at increased risk of social inequalities. The reduced access to healthcare typical of the oldest old, women and those with fewer socio-economic resources may compound communication difficulties and social isolation in people with dementia [17]. Socio-economic factors may be implicated in dementia aetiology [1]. Lower levels of education and worse physical health, which are strongly linked to deprivation, are associated with a greater dementia risk [2, 3]. Among people with dementia those from more deprived areas, women and older people are relatively less likely to receive anti-dementia drugs [18]. We aimed to investigate whether there are also social inequalities in physical preventative healthcare provision and psychotropic drug prescribing among people with dementia, and to compare these outcomes in people with and without dementia. We hypothesised, based on previous findings, that women and people from more deprived areas would access physical and mental healthcare less than their counterparts [4, 5]. We selected variables from The Health Improvement Network (THIN) primary care database to test these hypotheses, constrained by data availability. We judged that people with reduced healthcare access would be less likely to receive a dementia review, and more likely to be taking psychotropic medication, because medication for short-term treatments of challenging behaviour would be less frequently reviewed. We tested our hypotheses that people with dementia from more deprived areas, and women receive [1] more psychotropic medication [2], fewer surgery consultations [3], are less likely to have had blood pressure and weight monitoring and [4] an annual dementia review recorded in the last year, compared with those from less deprived areas and men.

Methods

Data

THIN primary care database contains anonymised information on twelve million patients from over 500 participating UK general practices (http://www.csdmruk.imshealth.com). General Practitioners (GPs) record information on symptoms and medical diagnoses using the Read hierarchical classification system [19], and information on prescriptions is entered onto the system automatically. Demographic information recorded for each patient includes sex, year of birth and Townsend deprivation score quintiles (see details below).

Study population

Individuals included in the study were under follow-up while aged 50 years or over during the period 2002–13, and had dementia, defined as a Read code for dementia (see Appendix 1 for code list) or an anti-dementia drug prescription (galantamine, rivastigmine, donepezil or memantine). We excluded individuals for whom deprivation score quintile data were not available (2%). For each practice, only data from the date of acceptable levels of computer usage and death recording were included, as inadequate recording of events before these dates may lead to incidence being underestimated [20, 21].

In this study, our focus was on people who were living outside long-term care facilities. We identified and excluded individuals who were likely to be resident in a long-term care facility, based on the assumption that households with five or more residents aged 70 or over on 1 January 2010 were such facilities. For the psychotropic drug prescribing prevalence and healthcare contact outcomes, patient data were additionally required to contain at least 6 months of follow-up. For each patient in the dementia cohort, we used a frequency matching approach to randomly select up to five patients not in the dementia cohort who were in the same practice, age group and the same sex at the start of follow-up.

Measurements

A list of Read codes for dementia diagnoses was developed using a published method [22]. We studied deprivation using Townsend score quintiles [23]. This area-level deprivation measure is calculated at the level of UK postcodes, using 2001 census data on unemployment, car ownership, home ownership and home overcrowding: quintiles are based on the whole UK population. Prescription data were used to determine initiation of antipsychotics, hypnotics and anxiolytics. Healthcare contact outcomes were, over a year: (i) number of surgery consultations; (ii) whether blood pressure and weight had been measured; (iii) whether there was a record that an annual dementia review (as required for the Quality Outcome Framework (QOF) payment [24]) had occurred. Reviews involve assessment of physical and mental health. Prevalence of an outcome was defined for each 1-year period as the proportion of those under follow-up during that period who had the outcome during that year. Covariates included sex, UK country, age, and, for the healthcare contact outcomes, a prescribing index as a measure of comorbidity (see details below). Age was analysed in 10-year categories. The prescribing index indicates the number of British National Formulary chapters from which patients received prescriptions (excluding anti-dementia drugs, vaccines and anaesthetics). This is a good measure for comorbidity [25].

Analysis

We analysed data using Stata version 13.1 (Stata Corp, College Station, Texas). For the period 2002–13, we estimated overall rates of initiation and prescribing prevalence of antipsychotics, hypnotics and anxiolytics; surgery consultations, annual blood pressure monitoring, annual weight monitoring and annual dementia review. We used multivariable Poisson regression to investigate the relationship between deprivation, gender and these outcomes. Random effects for general practices were included in models to account for variation in individual practices. Comparisons were made to the cohort of patients without dementia. Stratifying by Townsend quintile, incidence rate ratios were calculated for outcomes comparing the dementia cohort to the comparator non-dementia cohort.

Results

Included patients

A cohort of 68,061 patients was identified who had a record of dementia while aged 50 or over during the period 2002–13 (Supplementary data, Figure S1, available in Age and Ageing online); these patients were included in the analyses on psychotropic drug initiation. Of these, data were available from 54,721 (80%) for at least 6 months of follow-up, and so were included in the analyses on psychotropic drug prescribing prevalence and healthcare contact outcomes (Table 1). We included 259,337 people in our control population without dementia.

Table 1.

Characteristics of the included patients at first record of dementia

Characteristic Number (%)
Patients 68,061
Sex
Male 25,226 (37%)
Female 42,835 (63%)
Age (years)
50–59 1,344 (2%)
60–69 5,664 (8%)
70–79 20,678 (30%)
80–84 17,724 (26%)
85–89 14,652 (22%)
90+ 7,999 (12%)
Country
England 52,087 (77%)
Scotland 9,576 (14%)
Wales 4,260 (6%)
Northern Ireland 2,138 (3%)
Calendar year
2002–05 16,320 (24%)
2006–09 22,851 (34%)
2010–13 28,890 (42%)
Townsend quintile
1 (least deprived) 16,242 (24%)
2 15,366 (23%)
3 15,091 (22%)
4 12,976 (19%)
5 (most deprived) 8,386 (12%)
Prescribing index
Median (IQR) 4 (2–6)

Prescribing of psychotropic medication

The proportion of the 54,721 patients receiving at least one prescription in a calendar year increased up to 2009, but declined thereafter for antipsychotics, hypnotics and anxiolytics (Supplementary data, Figure S2(a)–(c) available in Age and Ageing). During 2013, 3.1% of the 21,716 under follow-up were prescribed antipsychotics, 2.4% were prescribed hypnotics and 2.6% were prescribed anxiolytics. During 2009, when the psychotropic drug prescribing prevalence was highest, 14.1% of the 16,043 then under follow-up were prescribed antipsychotics, 10.6% were prescribed hypnotics and 7.5% were prescribed anxiolytics. The proportion prescribed antipsychotics ranged from 6.8% to 8.0% in the deprivation groups; however, there was no systematic relationship between Townsend quintile and current prescribing of antipsychotics (Table 2). Women with dementia were more likely to be currently prescribed psychotropic medication than men with dementia. For example, 6.3% of men were currently receiving antipsychotics, compared to 7.7% of women, with an adjusted IRR (95% CI) of 1.18 (1.13–1.23).

Table 2.

IRRs for prescribing prevalence of antipsychotics, hypnotics and anxiolytics in 54,721 people with dementia, obtained from Poisson regression models with GP practice fitted as a random effecta,b

Covariate Antipsychotics Hypnotics Anxiolytics
% Univariable IRR (95% CI) Multivariable IRR (95% CI) % Univariable IRR (95% CI) Multivariable IRR (95% CI) % Univariable IRR (95% CI) Multivariable IRR (95% CI)
Townsend quintile
(least deprived)
1 7.0 1 1 5.5 1 1 3.9 1 1
2 7.1 0.98 (0.92–1.03) 0.97 (0.92–1.03) 5.8 1.04 (0.98–1.11) 1.03 (0.97–1.10) 4.6 1.07 (0.99–1.15) 1.06 (0.99–1.14)
3 8.0 1.07 (1.01–1.13) 1.07 (1.01–1.13) 5.5 0.96 (0.90–1.03) 0.96 (0.90–1.03) 4.6 1.08 (1.00–1.16) 1.07 (1.00–1.16)
4 6.8 0.95 (0.89–1.02) 0.95 (0.89–1.01) 5.2 0.96 (0.90–1.04) 0.96 (0.89–1.03) 3.8 0.92 (0.85–1.01) 0.92 (0.85–1.00)
(most deprived)
5 7.2 0.93 (0.87–1.00) 0.93 (0.87–1.00) 5.5 1.00 (0.92–1.08) 0.99 (0.91–1.07) 4.5 1.03 (0.94–1.13) 1.02 (0.93–1.12)
Sex
Male 6.3 1 1 5.1 1 1 3.9 1 1
Female 7.7 1.17 (1.13–1.22) 1.18 (1.13–1.23) 5.7 1.08 (1.04–1.13) 1.06 (1.02–1.12) 4.5 1.11 (1.05–1.16) 1.13 (1.07–1.19)
Age
50–69 4.7 0.61 (0.56–0.66) 0.61 (0.56–0.67) 2.9 0.52 (0.47–0.58) 0.52 (0.47–0.58) 3.0 0.64 (0.58–0.72) 0.64 (0.58–0.72)
70–79 7.9 1 1 5.8 1 1 4.7 1 1
80–84 7.3 0.89 (0.85–0.94) 0.89 (0.84–0.93) 5.7 0.95 (0.90–1.01) 0.95 (0.90–1.01) 4.3 0.88 (0.83–0.94) 0.87 (0.82–0.93)
85–89 7.2 0.87 (0.83–0.92) 0.83 (0.79–0.88) 5.8 0.96 (0.91–1.02) 0.94 (0.88–0.99) 4.2 0.86 (0.80–0.92) 0.82 (0.76–0.87)
90+ 7.2 0.86 (0.81–0.91) 0.82 (0.77–0.87) 5.9 0.98 (0.92–1.05) 0.96 (0.90–1.03) 4.2 0.84 (0.77–0.90) 0.79 (0.73–0.85)
Current year
2002–05 2.9 0.43 (0.39–0.46) 0.42 (0.39–0.46) 2.4 0.46 (0.42–0.50) 0.46 (0.42–0.50) 1.3 0.29 (0.25–0.32) 0.28 (0.25–0.32)
2006–09 9.4 1.33 (1.28–1.38) 1.32 (1.27–1.38) 7.1 1.32 (1.26–1.38) 1.32 (1.26–1.38) 4.8 0.99 (0.94–1.04) 0.98 (0.93–1.03)
2010–13 6.9 1 1 5.3 1 1 4.7 1 1

aRate per 100 person-years.

bEstimates from multivariable models adjusted for all other covariates, as well as for country.

Initiation of psychotropic medication

Overall, there was no systematic association between social deprivation and the initiation of antipsychotics, hypnotics or anxiolytics (Supplementary data, Table S1 available in Age and Ageing). Men with dementia were more likely to initiate all types of psychotropic medication than women with dementia.

Consultations and healthcare monitoring in people with dementia

The overall rate of surgery consultations was 6.8 visits per year, with no systematic change over time (Supplementary data, Figure S2(g) available in Age and Ageing). Annual blood pressure and weight monitoring both increased over time, and of the 21,716 patients who were under follow-up during 2013, blood pressure was recorded in 17,201 (79%) and weight was recorded in 10,118 (47%) (Supplementary data, Figure S2(d)–(e) available in Age and Ageing). From introduction in 2006, consistently around half of patients had a record of receiving an annual dementia review (Supplementary data, Figure S2(f) available in Age and Ageing). The crude rates and proportions of these outcomes were similar across deprivation score quintiles (Supplementary data, Figure S2 available in Age and Ageing; Table 3). Of the 11,273 patients with a dementia review during 2013, 5,657 (50%) had both weight and blood pressure recorded during that year: of the 10,443 patients under follow-up in 2013 who did not have a dementia review, 3,832 (37%) had both weight and blood pressure recorded during that year.

Table 3.

IRRs for each of the four healthcare contact outcomes in 54,721 people with dementia, from Poisson regression models with GP practice fitted as a random effect

Covariate Surgery consultations Blood pressure monitoring Weight monitoring Annual dementia review (for follow-up 2006 onwards)
Ratea Univariable IRR (95% CI) Multivariableb IRR (95% CI) % Univariable IRR (95% CI) Multivariableb IRR (95% CI) % Univariable IRR (95% CI) Multivariableb IRR (95% CI) % Univariable IRR (95% CI) Multivariableb IRR (95% CI)
Townsend quintile
(least deprived)
1 6.8 1 1 72 1 1 37 1 1 46 1 1
2 6.8 1.00 (1.00–1.01) 1.00 (0.99–1.00) 72 1.00 (0.98–1.01) 0.99 (0.98–1.01) 37 0.99 (0.96–1.01) 0.99 (0.96–1.01) 47 0.99 (0.97–1.02) 0.99 (0.97–1.01)
3 6.8 1.01 (1.00–1.02) 1.00 (1.00–1.01) 73 1.01 (0.99–1.03) 1.01)1.00 (0.99–1.02) 38 0.99 (0.97–1.02) 1.00 (0.97–1.03) 46 0.98 (0.96–1.01) 0.98 (0.95–1.00)
4 6.8 1.03 (1.03–1.04) 1.02 (1.01–1.02) 74 1.02 (1.00–1.04) 1.01 (0.99–1.03) 39 1.02 (0.99–1.04) 1.01 (0.99–1.04) 47 0.97 (0.94–0.99) 0.96 (0.94–0.99)
(most deprived)
5 6.5 1.02 (1.01–1.03) 1.00 (0.99–1.01) 75 1.03 (1.01–1.05) 1.02 (1.00–1.04) 40 1.02 (0.99–1.06) 1.02 (0.99–1.05) 48 0.97 (0.94–1.00) 0.97 (0.94–1.00)
Sex
Male 7.3 1 1 75 1 1 41 1 1 46 1 1
Female 6.5 0.89 (0.89–0.89) 0.90 (0.90–0.91) 72 0.97 (0.96–0.98) 0.96 (0.95–0.97) 36 0.87 (0.86–0.89) 0.91 (0.90–0.93) 47 1.02 (1.00–1.03) 1.01 (0.99–1.03)
Age
50–59 6.7 0.94 (0.93–0.96) 0.99 (0.97–1.00) 61 0.83 (0.78–0.87) 0.84 (0.80–0.89) 41 0.96 (0.90–1.03) 0.97 (0.91–1.04) 38 0.84 (0.78–0.90) 0.84 (0.78–0.91)
60–69 6.6 0.94 (0.94–0.95) 0.99 (0.98–0.99) 67 0.91 (0.89–0.94) 0.93 (0.90–0.95) 42 0.99 (0.96–1.03) 1.00 (0.97–1.03) 39 0.93 (0.90–0.96) 0.94 (0.90–0.97)
70–79 7.2 1 1 73 1 1 42 1 1 44 1 1
80–84 7.1 0.97 (0.96–0.97) 0.96 (0.95–0.96) 75 1.02 (1.00–1.04) 1.01 (1.00–1.03) 39 0.91 (0.89–0.93) 0.91 (0.89–0.93) 48 1.03 (1.01–1.05) 1.02 (1.00–1.04)
85–89 6.6 0.90 (0.90–0.91) 0.88 (0.88–0.89) 74 1.01 (1.00–1.03) 1.00 (0.98–1.01) 34 0.81 (0.79–0.83) 0.79 (0.77–0.81) 49 1.05 (1.03–1.07) 1.04 (1.02–1.06)
90+ 5.9 0.81 (0.80–0.81) 0.79 (0.78–0.79) 72 0.99 (0.97–1.01) 0.97 (0.95–0.99) 30 0.70 (0.68–0.72) 0.68 (0.66–0.70) 50 1.06 (1.03–1.08) 1.04 (1.01–1.06)
Current year
2002–05 6.7 0.96 (0.95–0.97) 1.03 (1.02–1.03) 64 0.83 (0.81–0.84) 0.85 (0.84–0.87) 24 0.56 (0.55–0.58) 0.57 (0.55–0.59)
2006–09 6.6 0.96 (0.96–0.97) 1.00 (1.00–1.01) 72 0.93 (0.92–0.94) 0.95 (0.94–0.96) 35 0.80 (0.79–0.82) 0.81 (0.80–0.83) 41 0.80 (0.78–0.81) 0.80 (0.79–0.82)
2010–13 6.9 1 1 77 1 1 43 1 1 50 1 1

aRate per person-year.

bEstimates from multivariable models adjusted for all other covariates, as well as for country and prescribing index.

Compared to men, women had lower rates of surgery consultations (6.5 per person-year in women and 7.3 per person-year in men; adjusted IRR 0.90, 95% CI 0.90–0.91), of annual blood pressure monitoring (72% in women and 75% in men; adjusted IRR 0.96, 95% CI 0.95–0.97) and of annual weight monitoring (36% in women and 41% in men; adjusted IRR 0.91, 95% CI 0.90–0.93).

Comparator cohort of patients without dementia

Rates of initiation of antipsychotics, hypnotics and anxiolytics were higher overall in the dementia cohort compared to the non-dementia cohort (Supplementary data, Table S2 available in Age and Ageing). People with dementia had fewer surgery consultations and were less likely to have their weight and blood pressure monitored at least annually, compared to the non-dementia group, with similar differences in each of the Townsend quintile strata (Supplementary data, Table S2 available in Age and Ageing).

Discussion

Area-level deprivation was not associated with healthcare or psychotropic medication receipt in people with dementia. Only half of people with dementia received an annual review as reimbursed by QOF. Among people with dementia, female gender was associated with receiving fewer primary care surgery consultations and less health monitoring. Men with dementia were more likely to be initiated on psychotropic drugs, but less likely to be currently taking them. Compared with our control population, people with dementia had fewer primary care consultations and were less likely to have weight and blood pressure monitored annually, despite the association of dementia with vascular risk factors, frailty and malnutrition [1], and were more likely to receive psychotropic medications.

Our findings differ from general population studies that found higher psychotropic prescribing levels in more deprived areas in people without dementia [26]. Perhaps government policies in the past decade, including targets incentivising GPs to identify and review annually people with dementia may have reduced inequities. One interpretation of our findings is that people with dementia, not having a family or friend carer to facilitate appointments may be the most important barrier to care, rather than socio-economic constraints per se. Interventions to increase understanding of dementia carers about the importance of maintaining physical health and treating co-morbidities may therefore be an important public health intervention.

Socio-economic prescribing inequalities often arise because patients or carers from less deprived groups better negotiate healthcare systems to seek out more desirable treatments. Socio-economic gradients in psychotropic prescribing have been attributed to differential access to alternate services such as psychological therapies, or different patient or carer expectations [26]. Perhaps this did not happen in people with dementia because there are few psychological, evidence based, routinely available treatments for behavioural and psychological symptoms of dementia [27], or because of the serious risks of initiating psychotropic drugs in dementia, although we did not find inequity before the MHRA warnings in 2009 [12]. In a previous study exploring the likelihood of patients with physical health complaints being referred to secondary care, inequalities associated with socio-economic circumstances occurred more in the absence of explicit guidance, whereas inequalities with older age and female gender were evident for all conditions [28].

Having a dementia diagnosis predicted receipt of fewer physical health checks and primary care contacts, despite the National Dementia Strategies prioritising healthcare access in this group. People with dementia often experience difficulties arranging, remembering and attending appointments. Women with dementia are reported to have more disability and disease than men with dementia [29], so it is concerning that they receive less health monitoring. Despite this, women were no less likely to receive an annual dementia review, suggesting that the content of reviews should be investigated, as preventative health monitoring should be an important component. Women more often live alone, due to their greater longevity [30]. The lesser likelihood of having a co-resident carer might explain why women with dementia access healthcare less.

Compared to men, women with dementia were less likely to be initiated on psychotropic medication, but overall more of these medications were prescribed to women indicating they took them for longer. More regular medication review could reduce unnecessary psychotropic prescribing. As we found that men accessed healthcare more frequently, there may have been more opportunities for review and reduction where possible in line with current guidelines [13]. In the general population, women are also more likely than men to be prescribed psychotropic medication [31, 32].

Limitations

Surgery contacts might be lower in people with dementia because they receive more home visits. We did not include home visits in analyses as there is uncertainty about how well they are recorded. Measures other than weight might be used to assess malnutrition on home visits. We could not identify people with undiagnosed dementia or control for dementia severity. As area-level deprivation can reduce access to secondary care where most dementia is diagnosed, there may have been more undiagnosed dementia in deprived areas; if this were so, it is likely that early-stage dementia would be most frequently missed due to symptom misattribution and delayed help-seeking [33]. This could mean that the people in more deprived areas had, on average, more severe dementia, but we did not find higher rates of psychotropic prescribing in these areas that might have suggested this. Women are more likely to move to a care home [34]. Those who remain at home might therefore have dementia which is on average less severe than men living at home. This could explain the lower rate of surgery consultations by women. The use of an area-level deprivation measure is a limitation, as individual deprivation level will sometimes be at odds to the deprivation level of the area in which a person lives.

Conclusion

Only half of people with dementia have an annual dementia review recorded, as recommended in UK guidelines and QOF. The QOF review for dementia has been associated with fewer unplanned hospital admissions, so increasing the proportion of patients who receive this may improve health outcomes [6]. In people with dementia, women received less physical healthcare monitoring, surgery visits and prescriptions for psychotropic drugs. A greater likelihood of women living alone without a family carer to help them access healthcare probably explains some of these findings. Enabling variables, such as having a carer to facilitate attending appointments have also been shown to be important determinants of people with dementias’ healthcare access in findings from other developed countries [7]. Interventions to improve access to physical healthcare and reduce psychotropic use in people with dementia, especially women, could benefit people with dementia, their families and society by enabling them to live well with dementia for longer.

Key points.

  • People with dementia received less primary, preventative healthcare than people without dementia.

  • Women with dementia received less primary, preventative healthcare than men with dementia.

  • Women with dementia were more likely to be taking psychotropic medication than men with dementia.

Supplementary Material

Supplementary Data

Acknowledgements

This work was supported by The Dunhill Medical Trust [grant number R296/0513].

Supplementary data

Supplementary data mentioned in the text are available to subscribers in Age and Ageing online.

Authors’ contributions

All authors devised the study; R.L. undertook all analyses and R.L. and C.C. drafted the paper. All authors were part of the Steering group that managed the study, of which C.C. was Principal Investigator. All authors revised the manuscript critically for intellectual content and approved the final version.

Conflicts of interest

None declared.

Ethics approval

The data provider of THIN (CSD Medical Research UK) has obtained overall ethical approval from the South East MREC. As we used anonymised routinely collected data in this study, we did not require further ethics approval, but we obtained approval by the THIN Scientific Review Committee. We did not recruit, approach or interview individual patients.

References

  • 1. Poblador-Plou B, Calderon-Larranaga A, Marta-Moreno J et al. . Comorbidity of dementia: a cross-sectional study of primary care older patients. BMC Psychiatry 2014; 14:84. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2. Laitinen ML, Bell JS, Lavikainen P, Lonnroos E, Sulkava R, Hartikainen S. Nationwide study of antipsychotic use among community-dwelling persons with Alzheimer's disease in Finland. Int Psychogeriatr 2011; 23(10):1623–31. [DOI] [PubMed] [Google Scholar]
  • 3. Schulze J, Glaeske G, van den Bussche H et al. . Prescribing of antipsychotic drugs in patients with dementia: a comparison with age-matched and sex-matched non-demented controls. Pharmacoepidemiol Drug Saf 2013; 22(12):1308–16. [DOI] [PubMed] [Google Scholar]
  • 4. Barnes TR, Banerjee S, Collins N, Treloar A, McIntyre SM, Paton C. Antipsychotics in dementia: prevalence and quality of antipsychotic drug prescribing in UK mental health services. Br J Psychiatry 2012; 201(3):221–6. [DOI] [PubMed] [Google Scholar]
  • 5. Luppa M Luck T, Braehler E, Koenig HH, Riedel-Heller SG. Prediction of institutionalisation in dementia - A systematic review. Dementia and geriatric cognitive disorders 2008; 26(1):65–78 [DOI] [PubMed] [Google Scholar]
  • 6. Bordier L, Doucet J, Boudet J, Bauduceau B. Update on cognitive decline and dementia in elderly patients with diabetes. Diabetes Metab 2014; 40(5):331–7. [DOI] [PubMed] [Google Scholar]
  • 7. Ballard C, Margallo-Lana M, Juszczak E et al. . Quetiapine and rivastigmine and cognitive decline in Alzheimer's disease: randomised double blind placebo controlled trial. Br Med J 2005; 330(7496):874–7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8. Langballe EM, Engdahl B, Nordeng H, Ballard C, Aarsland D, Selbaek G. Short- and long-term mortality risk associated with the use of antipsychotics among 26,940 dementia outpatients: a population-based study. Am J Geriatr Psychiatry 2014. Apr; 22(4):321–31. [DOI] [PubMed] [Google Scholar]
  • 9. Sterke CS, van Beeck EF, van d Velde N et al. . New insights: dose-response relationship between psychotropic drugs and falls: a study in nursing home residents with dementia. J Clin Pharmacol 2012; 52(6):947–55. [DOI] [PubMed] [Google Scholar]
  • 10. Bierman EJM, Comijs HC, Gundy CM, Sonnenberg C, Jonker C, Beekman ATF. The effect of chronic benzodiazepine use on cognitive functioning in older persons: good, bad or indifferent. Int J Geriatr Psychiatry 2007; 22(12):1194–200. [DOI] [PubMed] [Google Scholar]
  • 11. Rosenberg PB, Mielke MM, Han D et al. . The association of psychotropic medication use with the cognitive, functional, and neuropsychiatric trajectory of Alzheimer's disease. Int J Geriatr Psychiatry 2012. Dec; 27(12):1248–57. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12. Medicines and Healthcare products Regulatory Agency CoHM Antipsychotics: use in elderly people with dementia. Drug Saf Update 2009; 2: 8. [Google Scholar]
  • 13. Banerjee S. The Use of Antipsychotic Medication for People with Dementia: Time for Action. London: Department of Health, 2009. [Google Scholar]
  • 14. Martinez C, Jones RW, Rietbrock S. Trends in the prevalence of antipsychotic drug use among patients with Alzheimer's disease and other dementias including those treated with antidementia drugs in the community in the UK: a cohort study. BMJ Open 2013; 3(1):e002080. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15. Guthrie B, Clark SA, Reynish EL, McCowan C, Morales DR. Differential impact of two risk communications on antipsychotic prescribing to people with dementia in Scotland: segmented regression time series analysis 2001–2011. PLoS One 2013; 8(7):e68976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16. McIlroy G, Thomas SK, Coleman JJ. Second-generation antipsychotic drug use in hospital inpatients with dementia: the impact of a safety warning on rates of prescribing. J Public Health (Oxf) 2015; 37(2):346–52. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17. Hart JT. Inverse care law. Lancet 1971; 1(7696):405–&. [DOI] [PubMed] [Google Scholar]
  • 18. Cooper C, Lodwick R, Walters K et al. . Observational cohort study: deprivation and access to anti-dementia drugs in the UK. Age Ageing 2016; 45(1):148–54. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19. Booth N. What are the Read Codes. Health Libr Rev 1994; 11: 177–82. [DOI] [PubMed] [Google Scholar]
  • 20. Horsfall L, Walters K, Petersen I. Identifying periods of acceptable computer usage in primary care research databases. Pharmacoepidemiol Drug Saf 2013; 22(1):64–9. [DOI] [PubMed] [Google Scholar]
  • 21. Maguire A, Blak BT, Thompson M. The importance of defining periods of complete mortality reporting for research using automated data from primary care. Pharmacoepidemiol Drug Saf 2009; 18(1):76–83. [DOI] [PubMed] [Google Scholar]
  • 22. Dave S, Petersen I. Creating medical and drug code lists to identify cases in primary care databases. Pharmacoepidemiol Drug Saf 2009; 18(8):704–7. [DOI] [PubMed] [Google Scholar]
  • 23. Townsend P, Phillimore, M, Beattie A. Health and Deprivation: Inequality and the North. London: Croom Helm, 1988. [Google Scholar]
  • 24. Health and social care information centre Dementia rule set. Health and social care information centre 2014Available from: URL: http://www.hscic.gov.uk/media/15374/Dementia-rulesetv300/pdf/Dementia_ruleset_v30.0.pdf
  • 25. Brilleman SL, Salisbury C. Comparing measures of multimorbidity to predict outcomes in primary care: a cross sectional study. Fam Pract 2013; 30(2):172–8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26. Shah SM, Carey IM, Harris T, DeWilde S, Cook DG. Antipsychotic prescribing to older people living in care homes and the community in England and Wales. Int J Geriatr Psychiatry 2011; 26(4):423–34. [DOI] [PubMed] [Google Scholar]
  • 27. Livingston G, Kelly L, Lewis-Holmes E et al. . A systematic review of the clinical effectiveness and cost-effectiveness of sensory, psychological and behavioural interventions for managing agitation in older adults with dementia. Health Technol Assess 2014; 18(39):1–vi. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28. McBride D, Hardoon S, Walters K, Gilmour S, Raine R. Explaining variation in referral from primary to secondary care: cohort study. Br Med J 2010: 341. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29. Collerton J, Davies K, Jagger C et al. . Health and disease in 85 year olds: baseline findings from the Newcastle 85+ cohort study. BMJ 2009; 339: b4904. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30. Office of National Statistics Living alone in England and Wales. Office of National Statistics 2015. Available from: URL: http://www.ons.gov.uk/ons/rel/census/2011-census-analysis/do-the-demographic-and-socio-economic-characteristics-of-those-living-alone-in-england-and-wales-differ-from-the-general-population-/sty-living-alone-in-the-uk.html (10 October 2015, date last accessed).
  • 31. Cooper C, Bebbington P et al. . The treatment of common mental disorders across age groups: Results from the 2007 adult psychiatric morbidity survey. J Affect Disord 2010; 127(1–3):96–101. [DOI] [PubMed] [Google Scholar]
  • 32. Marston L, Nazareth I, Petersen I, Walters K, Osborn DP. Prescribing of antipsychotics in UK primary care: a cohort study. BMJ Open 2014; 4(12):e006135. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33. Feldman L, Wilcock J, Thuné-Boyle I, Iliffe S. Explaining the effects of symptom attribution by carers on help-seeking for individuals living with dementia. Dementia 1471301215593185, first published on June 30, 2015. doi:10.1177/1471301215593185. [DOI] [PubMed] [Google Scholar]
  • 34. McCann M, Donnelly M, O'Reilly D. Living arrangements, relationship to people in the household and admission to care homes for older people. Age Ageing 2011. May; 40(3):358–63. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Supplementary Data

Articles from Age and Ageing are provided here courtesy of Oxford University Press

RESOURCES