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A single-center model for implementation of SLEDAI documentation adherence in childhood-onset systemic lupus erythematosus (cSLE).
Nelson, Meghan Corrigan; Mosley, Colleen; Bennett, Tonya; Orenstein, Evan; Rouster-Stevens, Kelly.
Affiliation
  • Nelson MC; Department of Pediatrics, Emory University School of Medicine, Atlanta, GA, USA.
  • Mosley C; Children's Healthcare of Atlanta, Atlanta, GA, USA.
  • Bennett T; Children's Healthcare of Atlanta, Atlanta, GA, USA.
  • Orenstein E; Children's Healthcare of Atlanta, Atlanta, GA, USA.
  • Rouster-Stevens K; Department of Pediatrics, Emory University School of Medicine, Atlanta, GA, USA.
Lupus ; 32(12): 1447-1452, 2023 Oct.
Article in En | MEDLINE | ID: mdl-37807814
ABSTRACT

BACKGROUND:

Childhood-onset systemic lupus erythematosus (cSLE) is an autoimmune disease with variable disease expression but noted association with significant disease-related damage, morbidity, and mortality. The European Alliance of Associations for Rheumatology (EULAR) recommends routine monitoring of SLE through validated disease activity and chronicity indices, including the Systemic Lupus Erythematosus Disease Activity Index (SLEDAI). Despite this, physician adherence with SLEDAI documentation remains elusive at various academic institutions. The aim of our study was to determine baseline SLEDAI documentation rates at our center and assess the change in adherence in SLEDAI documentation rate with electronic clinical decision support (CDS) reminders facilitated through the electronic medical record (EMR) over a 2-year period.

METHODS:

All SLE encounters over a 24-month period at a pediatric academic center were reviewed in order to obtain baseline SLEDAI documentation percentages. Physicians subsequently received monthly email reminders, initiated at month 4 of project initiation, with subsequent CDS reminder 13 months after project initiation prompted by anti-dsDNA lab result. Chart review was repeated continuously for each provider, and SLEDAI documentation rates were emailed to each provider monthly. Physicians completed a post-intervention survey regarding barriers to SLEDAI documentation at the end of the study.

RESULTS:

A total of 1980 SLE encounters were reviewed for this study. Baseline SLEDAI documentation rates were 10%. Following the introduction of monthly emails reminding physicians to document SLEDAI, rates increased to 55%. After the initiation of electronic in-basket reminders prompted by lab results, rates increased to 60%. Noted barriers to documentation were cited to be forgetfulness (67%) and lack of time (33%).

CONCLUSION:

Our study demonstrates that monthly email reminders as well as EMR-mediated electronic in-basket reminders increased SLEDAI documentation rates at an academic center. Noted barriers to documentation were reported to be forgetfulness (67%) and lack of time (33%).
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Lupus Erythematosus, Systemic Type of study: Prognostic_studies Limits: Child / Humans Language: En Journal: Lupus Journal subject: REUMATOLOGIA Year: 2023 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Lupus Erythematosus, Systemic Type of study: Prognostic_studies Limits: Child / Humans Language: En Journal: Lupus Journal subject: REUMATOLOGIA Year: 2023 Document type: Article Affiliation country:
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