{"title":"Diagnostic test accuracy of telehealth assessment for dementia and mild cognitive impairment.","authors":"Jenny McCleery, Julian Laverty, Terry J Quinn","doi":"10.1002/14651858.CD013786.pub2","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>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.</p><p><strong>Objectives: </strong>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.</p><p><strong>Search methods: </strong>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.</p><p><strong>Selection criteria: </strong>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.</p><p><strong>Data collection and analysis: </strong>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.</p><p><strong>Main results: </strong>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.</p><p><strong>Authors' conclusions: </strong>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.</p>","PeriodicalId":515753,"journal":{"name":"The Cochrane database of systematic reviews","volume":" ","pages":"CD013786"},"PeriodicalIF":0.0000,"publicationDate":"2021-07-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/14651858.CD013786.pub2","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Cochrane database of systematic reviews","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1002/14651858.CD013786.pub2","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 3
Abstract
Background: 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.
Objectives: 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.
Search methods: 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.
Selection criteria: 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.
Data collection and analysis: 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.
Main results: 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.
Authors' conclusions: 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.
背景:世界各地有数百万痴呆症患者未得到诊断,这对他们获得护理和治疗以及合理的服务规划都产生了负面影响。远程保健——利用信息和通信技术(ICT)提供远程保健服务——可能是增加疑似痴呆症患者获得专家评估的一种方式,特别是那些生活在偏远或农村地区的人。在2019冠状病毒病大流行期间,它也得到了广泛使用。重要的是要知道,使用远程医疗评估做出的诊断是否与传统的面对面临床环境做出的诊断一样准确。目的:主要目的:评估远程医疗评估对痴呆和轻度认知障碍的诊断准确性。次要目标:确定相关研究证据的质量和数量;识别测试精度数据的异质性来源;识别和综合所纳入研究中关于患者或临床医生满意度、资源使用、成本或远程保健评估模型可行性的任何数据。检索方法:我们于2020年11月4日检索了多个数据库和临床试验注册库,检索了已发表的和“灰色”文献和已注册的试验。我们没有使用搜索过滤器和语言限制。我们对检索到的引文一式两份进行筛选,并对认为可能相关的论文全文一式两份进行评估。选择标准:我们纳入了有10名或更多参与者的横断面研究,这些参与者被转介到专家服务机构评估疑似认知障碍。在一个月或更短的时间内,每个参与者必须接受两项旨在诊断痴呆症或轻度认知障碍(MCI)的临床评估:远程保健评估(指数测试)和传统的面对面评估(参考标准)。远程保健评估可以通过面对面收集的一些数据来提供信息,例如,由从事初级保健工作的护士提供信息,但患者与负责综合信息和作出诊断的专业临床医生之间的所有联系都必须使用信通技术远程进行。资料收集和分析:两位综述作者独立地从纳入的研究中提取数据。提取的数据包括研究设计、设置、参与者、指标测试的细节和参考标准,以及以被诊断为痴呆或轻度认知障碍的参与者人数的形式显示的结果。研究还寻求了痴呆症亚型诊断和患者或临床医生满意度、资源使用、成本和可行性的定量测量数据。我们使用QUADAS-2评估每个纳入研究的偏倚风险和适用性。我们将结果输入2x2表格,以计算远程医疗评估诊断全因痴呆、轻度认知损伤和任何认知综合征(合并痴呆和轻度认知损伤)的敏感性和特异性。我们以叙述的方式呈现纳入研究的结果,因为研究太少,无法得出敏感性和特异性的总结性估计。主要结果:3项研究136名受试者符合纳入条件。两项研究(20和100名参与者)在澳大利亚的社区环境中进行,一项研究(16名参与者)在美国的退伍军人之家进行。参与者从初级保健转来,未确诊的认知症状或在养老院的筛查测试中被确定为患痴呆症的高风险。痴呆和轻度认知障碍是更大规模研究的目标条件;其他的研究只针对痴呆症的诊断。只有一项小型研究使用了“纯”远程医疗模式,即不涉及任何面对面评估的要素。这些研究总体上进行得很好。我们认为有两项研究存在纳入偏倚的高风险,因为护士面对面收集的大量信息被用于指标测试和参考标准评估。一项研究存在不明确的选择偏倚风险。对于全因痴呆的诊断,远程医疗评估的敏感性为0.80 ~ 1.00,特异性为0.80 ~ 1.00。由于研究之间的不精确性、不一致性和偏倚风险,我们认为这是非常低确定性的证据。对于MCI的诊断,仅有一项研究(100名参与者)的数据给出了0.71的敏感性(95% CI 0.54至0.84)和0.73的特异性(95% CI 0.60至0.84)。由于不精确和偏倚风险,我们认为这是低确定性证据。对于任何认知综合征(痴呆或MCI)的诊断,同一研究的数据给出的敏感性为0.97 (95% CI 0.91至0.99),特异性为0.22 (95% CI 0.03至0.60)。大多数诊断上的分歧是关于MCI和痴呆之间的区别,在这两个方向上的差异大致相等。 在面对面评估中被确定为认知健康的患者在远程健康评估中也有被诊断为轻度认知障碍的趋势(但数量很少)。没有足够的数据来评估痴呆亚型诊断的准确性。一项研究提供了少量数据,表明临床医生,特别是患者对远程保健模式的满意程度很高。没有关于资源使用、成本或可行性的数据。作者的结论:我们只发现了很少的符合条件的研究,参与者也很少。为分析提供数据的研究之间的一个重要区别是目标条件是仅为痴呆(两项研究)还是痴呆和轻度认知障碍(一项研究)。数据表明,在对照传统面对面评估的参考标准进行评估时,远程医疗评估可能对全因痴呆的诊断具有高度敏感性和特异性,但由于样本量小和研究之间的异质性,估计结果并不精确,并且可能主要适用于远程医疗模型,这些模型包括与负责诊断的医生以外的医疗保健专业人员进行大量面对面接触。对于通过远程医疗评估诊断轻度认知损伤,灵敏度和特异性的最佳估计略低,但基于单一研究。错误发生在认知健康/MCI和MCI/痴呆边界。然而,没有证据表明诊断分歧比预期的更频繁,因为在分配痴呆诊断时,临床医生之间的意见存在已知的差异。