Matches in SemOpenAlex for { <https://semopenalex.org/work/W3106070778> ?p ?o ?g. }
- W3106070778 abstract "Many millions of people living with dementia around the world are not diagnosed, which has a negative impact both on their access to care and treatment and on rational service planning. Telehealth - the use of information and communication technology (ICT) to provide health services at a distance - may be a way to increase access to specialist assessment for people with suspected dementia, especially those living in remote or rural areas. It has also been much used during the COVID-19 pandemic. It is important to know whether diagnoses made using telehealth assessment are as accurate as those made in conventional, face-to-face clinical settings.Primary objective: to assess the diagnostic accuracy of telehealth assessment for dementia and mild cognitive impairment. Secondary objectives: to identify the quality and quantity of the relevant research evidence; to identify sources of heterogeneity in the test accuracy data; to identify and synthesise any data on patient or clinician satisfaction, resource use, costs or feasibility of the telehealth assessment models in the included studies.We searched multiple databases and clinical trial registers on 4 November 2020 for published and 'grey' literature and registered trials. We applied no search filters and no language restrictions. We screened the retrieved citations in duplicate and assessed in duplicate the full texts of papers considered potentially relevant.We included in the review cross-sectional studies with 10 or more participants who had been referred to a specialist service for assessment of a suspected cognitive disorder. Within a period of one month or less, each participant had to undergo two clinical assessments designed to diagnose dementia or mild cognitive impairment (MCI): a telehealth assessment (the index test) and a conventional face-to-face assessment (the reference standard). The telehealth assessment could be informed by some data collected face-to-face, e.g. by nurses working in primary care, but all contact between the patient and the specialist clinician responsible for synthesising the information and making the diagnosis had to take place remotely using ICT.Two review authors independently extracted data from included studies. Data extracted covered study design, setting, participants, details of index test and reference standard, and results in the form of numbers of participants given diagnoses of dementia or MCI. Data were also sought on dementia subtype diagnoses and on quantitative measures of patient or clinician satisfaction, resource use, costs and feasibility. We assessed risk of bias and applicability of each included study using QUADAS-2. We entered the results into 2x2 tables in order to calculate the sensitivity and specificity of telehealth assessment for the diagnosis of all-cause dementia, MCI, and any cognitive syndrome (combining dementia and MCI). We presented the results of included studies narratively because there were too few studies to derive summary estimates of sensitivity and specificity.Three studies with 136 participants were eligible for inclusion. Two studies (20 and 100 participants) took place in community settings in Australia and one study (16 participants) was conducted in veterans' homes in the USA. Participants were referred from primary care with undiagnosed cognitive symptoms or were identified as being at high risk of having dementia on a screening test in the care homes. Dementia and MCI were target conditions in the larger study; the other studies targeted dementia diagnosis only. Only one small study used a 'pure' telehealth model, i.e. not involving any elements of face-to-face assessment. The studies were generally well-conducted. We considered two studies to be at high risk of incorporation bias because a substantial amount of information collected face-to-face by nurses was used to inform both index test and reference standard assessments. One study was at unclear risk of selection bias. For the diagnosis of all-cause dementia, sensitivity of telehealth assessment ranged from 0.80 to 1.00 and specificity from 0.80 to 1.00. We considered this to be very low-certainty evidence due to imprecision, inconsistency between studies and risk of bias. For the diagnosis of MCI, data were available from only one study (100 participants) giving a sensitivity of 0.71 (95% CI 0.54 to 0.84) and a specificity of 0.73 (95% CI 0.60 to 0.84). We considered this to be low-certainty evidence due to imprecision and risk of bias. For diagnosis of any cognitive syndrome (dementia or MCI), data from the same study gave a sensitivity of 0.97 (95% CI 0.91 to 0.99) and a specificity of 0.22 (95% CI 0.03 to 0.60). The majority of diagnostic disagreements concerned the distinction between MCI and dementia, occurring approximately equally in either direction. There was also a tendency for patients identified as cognitively healthy at face-to-face assessment to be diagnosed with MCI at telehealth assessment (but numbers were small). There were insufficient data to make any assessment of the accuracy of dementia subtype diagnosis. One study provided a small amount of data indicating a good level of clinician and especially patient satisfaction with the telehealth model. There were no data on resource use, costs or feasibility.We found only very few eligible studies with a small number of participants. An important difference between the studies providing data for the analyses was whether the target condition was dementia only (two studies) or dementia and MCI (one study). The data suggest that telehealth assessment may be highly sensitive and specific for the diagnosis of all-cause dementia when assessed against a reference standard of conventional face-to-face assessment, but the estimates are imprecise due to small sample sizes and between-study heterogeneity, and may apply mainly to telehealth models which incorporate a considerable amount of face-to-face contact with healthcare professionals other than the doctor responsible for making the diagnosis. For the diagnosis of MCI by telehealth assessment, best estimates of both sensitivity and specificity were somewhat lower, but were based on a single study. Errors occurred at the cognitively healthy/MCI and the MCI/dementia boundaries. However, there is no evidence that diagnostic disagreements were more frequent than would be expected due to the known variation between clinicians' opinions when assigning a dementia diagnosis." @default.
- W3106070778 created "2020-11-23" @default.
- W3106070778 creator A5043572219 @default.
- W3106070778 creator A5056395692 @default.
- W3106070778 creator A5090549322 @default.
- W3106070778 date "2021-07-20" @default.
- W3106070778 modified "2023-10-03" @default.
- W3106070778 title "Diagnostic test accuracy of telehealth assessment for dementia and mild cognitive impairment" @default.
- W3106070778 cites W1552002442 @default.
- W3106070778 cites W1552510057 @default.
- W3106070778 cites W1836511861 @default.
- W3106070778 cites W1968038365 @default.
- W3106070778 cites W2006609651 @default.
- W3106070778 cites W2014040096 @default.
- W3106070778 cites W2049134811 @default.
- W3106070778 cites W2068992609 @default.
- W3106070778 cites W2069778485 @default.
- W3106070778 cites W2069902131 @default.
- W3106070778 cites W2073439217 @default.
- W3106070778 cites W2092259308 @default.
- W3106070778 cites W2115017507 @default.
- W3106070778 cites W2123963100 @default.
- W3106070778 cites W2131645385 @default.
- W3106070778 cites W2134910738 @default.
- W3106070778 cites W2141057841 @default.
- W3106070778 cites W2145672185 @default.
- W3106070778 cites W2169792285 @default.
- W3106070778 cites W2170949346 @default.
- W3106070778 cites W2336452711 @default.
- W3106070778 cites W2471554802 @default.
- W3106070778 cites W2561538311 @default.
- W3106070778 cites W2582524520 @default.
- W3106070778 cites W2731267925 @default.
- W3106070778 cites W2943828894 @default.
- W3106070778 cites W2947339359 @default.
- W3106070778 cites W2951787623 @default.
- W3106070778 cites W2995668974 @default.
- W3106070778 cites W3106070778 @default.
- W3106070778 cites W3135723836 @default.
- W3106070778 cites W4210340856 @default.
- W3106070778 cites W4246509836 @default.
- W3106070778 cites W4247665917 @default.
- W3106070778 doi "https://doi.org/10.1002/14651858.cd013786.pub2" @default.
- W3106070778 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/8406800" @default.
- W3106070778 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/34282852" @default.
- W3106070778 hasPublicationYear "2021" @default.
- W3106070778 type Work @default.
- W3106070778 sameAs 3106070778 @default.
- W3106070778 citedByCount "8" @default.
- W3106070778 countsByYear W31060707782021 @default.
- W3106070778 countsByYear W31060707782022 @default.
- W3106070778 countsByYear W31060707782023 @default.
- W3106070778 crossrefType "journal-article" @default.
- W3106070778 hasAuthorship W3106070778A5043572219 @default.
- W3106070778 hasAuthorship W3106070778A5056395692 @default.
- W3106070778 hasAuthorship W3106070778A5090549322 @default.
- W3106070778 hasBestOaLocation W31060707782 @default.
- W3106070778 hasConcept C136264566 @default.
- W3106070778 hasConcept C142724271 @default.
- W3106070778 hasConcept C151730666 @default.
- W3106070778 hasConcept C15744967 @default.
- W3106070778 hasConcept C160735492 @default.
- W3106070778 hasConcept C162324750 @default.
- W3106070778 hasConcept C17744445 @default.
- W3106070778 hasConcept C199539241 @default.
- W3106070778 hasConcept C2777267654 @default.
- W3106070778 hasConcept C2779134260 @default.
- W3106070778 hasConcept C2779473830 @default.
- W3106070778 hasConcept C2779483572 @default.
- W3106070778 hasConcept C2779891985 @default.
- W3106070778 hasConcept C2780378061 @default.
- W3106070778 hasConcept C2781050511 @default.
- W3106070778 hasConcept C50522688 @default.
- W3106070778 hasConcept C534262118 @default.
- W3106070778 hasConcept C61904560 @default.
- W3106070778 hasConcept C71924100 @default.
- W3106070778 hasConcept C86803240 @default.
- W3106070778 hasConceptScore W3106070778C136264566 @default.
- W3106070778 hasConceptScore W3106070778C142724271 @default.
- W3106070778 hasConceptScore W3106070778C151730666 @default.
- W3106070778 hasConceptScore W3106070778C15744967 @default.
- W3106070778 hasConceptScore W3106070778C160735492 @default.
- W3106070778 hasConceptScore W3106070778C162324750 @default.
- W3106070778 hasConceptScore W3106070778C17744445 @default.
- W3106070778 hasConceptScore W3106070778C199539241 @default.
- W3106070778 hasConceptScore W3106070778C2777267654 @default.
- W3106070778 hasConceptScore W3106070778C2779134260 @default.
- W3106070778 hasConceptScore W3106070778C2779473830 @default.
- W3106070778 hasConceptScore W3106070778C2779483572 @default.
- W3106070778 hasConceptScore W3106070778C2779891985 @default.
- W3106070778 hasConceptScore W3106070778C2780378061 @default.
- W3106070778 hasConceptScore W3106070778C2781050511 @default.
- W3106070778 hasConceptScore W3106070778C50522688 @default.
- W3106070778 hasConceptScore W3106070778C534262118 @default.
- W3106070778 hasConceptScore W3106070778C61904560 @default.
- W3106070778 hasConceptScore W3106070778C71924100 @default.
- W3106070778 hasConceptScore W3106070778C86803240 @default.
- W3106070778 hasIssue "7" @default.
- W3106070778 hasLocation W31060707781 @default.
- W3106070778 hasLocation W31060707782 @default.