Literature DB >> 28567555

Toward electronic health recording: evaluation of electronic patient reported outcome measures (e-PROMs) system for remote monitoring of early systemic lupus patients.

Y El Miedany1,2, M El Gaafary3, Nadia El Aroussy4, S Bahlas5, M Hegazi6, D Palmer7, S Youssef4.   

Abstract

The study aimed to assess the value of evaluation of electronic patient reported outcome measures (e-PROMs) in the assessment and management of SLE disease activity flares, its association with adherence to therapy as well as organ damage. A randomized, controlled crossover study was carried out over a 24-month duration. One hundred forty-seven SLE patients meeting the revised American College of Rheumatology (ACR) criteria were enrolled. Systemic Lupus Erythematosus Disease Activity Index (SLEDAI) was used to assess disease activity, whereas organ damage was scored using the Systemic Lupus International Collaborating Clinics (SLICC)/ACR Damage Index. In the first 12 months, the patients were assessed every 3 months. At 12 months, the patients were randomized into a cohort of 73 patients who continued their care in the same style and 74 patients who completed an online e-PROMs questionnaire on monthly basis for another 12-month period. The data captured were then retrospectively analyzed at the end of the 24-month study period. At the end of the first year of the study, the mean SLEDAI and SDI scores were 8.72 (6.1) and 1.9 (2.2). At the end of the second year, the mean SLEDAI and SDI scores in the e-PROMs cohort were 3.1 (2.6) and 1.2 (1.3), whereas in the control group, the scores were 7.63 (6.7) and 1.8 (2.3), respectively (p < 0.01). Adjusting for possible confounding variables, the number of flares, regardless of their severity, was associated with damage accrual (OR 2.03, 95% CI 1.34 to 2.83, p < 0.001). Adherence to therapy was significantly (p < 0.1) higher in the e-PROMs group. e-PROMs was equivalent to PROMs paper format and has a potential disease-modifying effect as it facilitated close monitoring of disease activity with an option of management escalation whenever indicated.

Entities:  

Keywords:  Adherence; Early SLE; Patient motivation questionnaire; Patient reported outcome measures; Rheumote; e-PROMs

Mesh:

Substances:

Year:  2017        PMID: 28567555     DOI: 10.1007/s10067-017-3675-9

Source DB:  PubMed          Journal:  Clin Rheumatol        ISSN: 0770-3198            Impact factor:   2.980


  35 in total

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Authors:  M Bandeira; S Buratti; M Bartoli; C Gasparini; L Breda; A Pistorio; S Grassi; M G Alpigiani; G Barbano; L L Janz-Junior; A Martini; A Ravelli
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Journal:  Lupus       Date:  2009-10-30       Impact factor: 2.911

Review 3.  Electronic patient-reported outcome systems in oncology clinical practice.

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Review 4.  Epidemiology of systemic lupus erythematosus: a comparison of worldwide disease burden.

Authors:  N Danchenko; J A Satia; M S Anthony
Journal:  Lupus       Date:  2006       Impact factor: 2.911

5.  The number of flares patients experience impacts on damage accrual in systemic lupus erythematosus: data from a multiethnic Latin American cohort.

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Review 6.  Quality indicators in rheumatoid arthritis care: using measurement to promote quality improvement.

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Authors:  Yasser El Miedany; Deborah Palmer
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8.  Measuring quality of life in routine oncology practice improves communication and patient well-being: a randomized controlled trial.

Authors:  Galina Velikova; Laura Booth; Adam B Smith; Paul M Brown; Pamela Lynch; Julia M Brown; Peter J Selby
Journal:  J Clin Oncol       Date:  2004-02-15       Impact factor: 44.544

Review 9.  The geoepidemiology of systemic lupus erythematosus.

Authors:  Andrea T Borchers; Stanley M Naguwa; Yehuda Shoenfeld; M Eric Gershwin
Journal:  Autoimmun Rev       Date:  2009-12-24       Impact factor: 9.754

10.  Response rates for patient-reported outcomes using web-based versus paper questionnaires: comparison of two invitational methods in older colorectal cancer patients.

Authors:  Nicole Je Horevoorts; Pauline Aj Vissers; Floortje Mols; Melissa Sy Thong; Lonneke V van de Poll-Franse
Journal:  J Med Internet Res       Date:  2015-05-07       Impact factor: 5.428

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  3 in total

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Authors:  Julie Gandrup; Jinoos Yazdany
Journal:  Rheum Dis Clin North Am       Date:  2019-05       Impact factor: 2.670

2.  Using Electronic Data Collection Platforms to Assess Complementary and Integrative Health Patient-Reported Outcomes: Feasibility Project.

Authors:  Jolie N Haun; Amy C Alman; Christine Melillo; Maisha Standifer; Julie McMahon-Grenz; Marlena Shin; W A Lapcevic; Nitin Patel; A Rani Elwy
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Review 3.  The role of medical data in efficient patient care delivery: a review.

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