Accuracy, patient-perceived usability, and acceptance of two symptom checkers (Ada and Rheport) in rheumatology: interim results from a randomized controlled crossover trial.

IF 4.4 2区 医学 Q1 RHEUMATOLOGY
Johannes Knitza, Jacob Mohn, Christina Bergmann, Eleni Kampylafka, Melanie Hagen, Daniela Bohr, Harriet Morf, Elizabeth Araujo, Matthias Englbrecht, David Simon, Arnd Kleyer, Timo Meinderink, Wolfgang Vorbrüggen, Cay Benedikt von der Decken, Stefan Kleinert, Andreas Ramming, Jörg H W Distler, Nicolas Vuillerme, Achim Fricker, Peter Bartz-Bazzanella, Georg Schett, Axel J Hueber, Martin Welcker
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引用次数: 0

Abstract

Background: Timely diagnosis and treatment are essential in the effective management of inflammatory rheumatic diseases (IRDs). Symptom checkers (SCs) promise to accelerate diagnosis, reduce misdiagnoses, and guide patients more effectively through the health care system. Although SCs are increasingly used, there exists little supporting evidence.

Objective: To assess the diagnostic accuracy, patient-perceived usability, and acceptance of two SCs: (1) Ada and (2) Rheport.

Methods: Patients newly presenting to a German secondary rheumatology outpatient clinic were randomly assigned in a 1:1 ratio to complete Ada or Rheport and consecutively the respective other SCs in a prospective non-blinded controlled randomized crossover trial. The primary outcome was the accuracy of the SCs regarding the diagnosis of an IRD compared to the physicians' diagnosis as the gold standard. The secondary outcomes were patient-perceived usability, acceptance, and time to complete the SC.

Results: In this interim analysis, the first 164 patients who completed the study were analyzed. 32.9% (54/164) of the study subjects were diagnosed with an IRD. Rheport showed a sensitivity of 53.7% and a specificity of 51.8% for IRDs. Ada's top 1 (D1) and top 5 disease suggestions (D5) showed a sensitivity of 42.6% and 53.7% and a specificity of 63.6% and 54.5% concerning IRDs, respectively. The correct diagnosis of the IRD patients was within the Ada D1 and D5 suggestions in 16.7% (9/54) and 25.9% (14/54), respectively. The median System Usability Scale (SUS) score of Ada and Rheport was 75.0/100 and 77.5/100, respectively. The median completion time for both Ada and Rheport was 7.0 and 8.5 min, respectively. Sixty-four percent and 67.1% would recommend using Ada and Rheport to friends and other patients, respectively.

Conclusions: While SCs are well accepted among patients, their diagnostic accuracy is limited to date.

Trial registration: DRKS.de, DRKS00017642 . Registered on 23 July 2019.

Abstract Image

Abstract Image

风湿病学中两种症状检查器(Ada 和 Rheport)的准确性、患者感知可用性和接受度:随机对照交叉试验的中期结果。
背景:及时诊断和治疗是有效管理炎症性风湿病(IRDs)的关键。症状检查器(SC)有望加快诊断、减少误诊,并通过医疗保健系统更有效地指导患者。虽然 SC 的使用越来越多,但支持它的证据却很少:目的:评估两种 SC:(1)Ada 和(2)Rheport 的诊断准确性、患者认为的可用性和接受度:方法:在一项前瞻性非盲对照随机交叉试验中,新到德国二级风湿病门诊就诊的患者按 1:1 的比例被随机分配完成 Ada 或 Rheport 以及相应的其他 SC。主要结果是与作为金标准的医生诊断相比,SC 对 IRD 诊断的准确性。次要结果是患者认为的可用性、接受度和完成 SC 所需的时间:在本次中期分析中,对完成研究的前 164 名患者进行了分析。32.9%的研究对象(54/164)被诊断为IRD。Rheport 对 IRD 的灵敏度为 53.7%,特异度为 51.8%。Ada的前1种疾病建议(D1)和前5种疾病建议(D5)对IRD的敏感性分别为42.6%和53.7%,特异性分别为63.6%和54.5%。对 IRD 患者的正确诊断在 Ada D1 和 D5 建议范围内的分别占 16.7%(9/54)和 25.9%(14/54)。Ada和Rheport的系统可用性量表(SUS)中位数分别为75.0/100和77.5/100。Ada 和 Rheport 的中位完成时间分别为 7.0 分钟和 8.5 分钟。64%和67.1%的患者会向朋友和其他患者推荐使用Ada和Rheport:结论:虽然SC在患者中的接受度很高,但其诊断准确性至今仍然有限:DRKS.de, DRKS00017642 .注册日期:2019 年 7 月 23 日。
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来源期刊
CiteScore
8.30
自引率
2.00%
发文量
261
审稿时长
2.3 months
期刊介绍: Established in 1999, Arthritis Research and Therapy is an international, open access, peer-reviewed journal, publishing original articles in the area of musculoskeletal research and therapy as well as, reviews, commentaries and reports. A major focus of the journal is on the immunologic processes leading to inflammation, damage and repair as they relate to autoimmune rheumatic and musculoskeletal conditions, and which inform the translation of this knowledge into advances in clinical care. Original basic, translational and clinical research is considered for publication along with results of early and late phase therapeutic trials, especially as they pertain to the underpinning science that informs clinical observations in interventional studies.
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