Clinical diagnosis of Lewy body dementia. Issue 4 (July 2020)

• Record Type: Journal Article
• Authors: Surendranathan, Ajenthan; Kane, Joseph P. M.; Bentley, Allison; Barker, Sally A. H.; Taylor, John-Paul; Thomas, Alan J.; Allan, Louise M.; McNally, Richard J.; James, Peter W.; McKeith, Ian G.; Burn, David J.; O'Brien, John T.
• Is Part Of: BJPsych open. Volume 6:Issue 4(2020)
• Publication Date: 2020-07
• Subjects: Dementia, -- clinical neurology, -- epidemiology, -- outpatient treatment, -- comorbidity; Psychiatry -- Periodicals; Mental health -- Periodicals; 616.89005
• DOI: 10.1192/bjo.2020.44
• Languages: English
• ISSNs: 2056-4724

Abstract

Abstract : Background: Lewy body dementia, consisting of both dementia with Lewy bodies (DLB) and Parkinson's disease dementia (PDD), is considerably under-recognised clinically compared with its frequency in autopsy series. Aims: This study investigated the clinical diagnostic pathways of patients with Lewy body dementia to assess if difficulties in diagnosis may be contributing to these differences. Method: We reviewed the medical notes of 74 people with DLB and 72 with non-DLB dementia matched for age, gender and cognitive performance, together with 38 people with PDD and 35 with Parkinson's disease, matched for age and gender, from two geographically distinct UK regions. Results: The cases of individuals with DLB took longer to reach a final diagnosis (1.2 v . 0.6 years, P = 0.017), underwent more scans (1.7 v . 1.2, P = 0.002) and had more alternative prior diagnoses (0.8 v . 0.4, P = 0.002), than the cases of those with non-DLB dementia. Individuals diagnosed in one region of the UK had significantly more core features (2.1 v . 1.5, P = 0.007) than those in the other region, and were less likely to have dopamine transporter imaging ( P < 0.001). For patients with PDD, more than 1.4 years prior to receiving a dementia diagnosis: 46% (12 of 26) had documented impaired activities of daily living because of cognitive impairment, 57% (16 of 28) had cognitive impairment in multiple domains, with 38% (6 of 16) having both, and 39% (9 of 23) already receiving anti-dementia drugs. Conclusions: Our results show the pathway to diagnosis of DLB is longer and more complex than for non-DLB dementia. There were also marked differences between regions in the thresholds clinicians adopt for diagnosing DLB and also in the use of dopamine transporter imaging. For PDD, a diagnosis of dementia was delayed well beyond symptom onset and even treatment.