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Association Between Patient-Reported Outcomes and Treatment Failure in Juvenile Idiopathic Arthritis
Alysha Taxter1, Brittany C Donaldson2, Joseph Rigdon2
1Nationwide Children's Hospital, Columbus, Ohio.
Insights
Higher energy and longer symptom duration before diagnosis in children with juvenile idiopathic arthritis (JIA) were linked to better treatment outcomes. This suggests patient-reported data can improve JIA therapy effectiveness.
Area of Science:
- Pediatric Rheumatology
- Clinical Outcomes Research
- Patient-Reported Outcomes
Background:
- Juvenile idiopathic arthritis (JIA) diagnosis is often preceded by months of symptoms.
- Understanding factors influencing treatment response in JIA is crucial for improving patient care.
Purpose of the Study:
- To determine if baseline patient-reported outcomes (PROs) predict changes in JIA pharmacotherapy.
- To investigate the association between pre-diagnosis symptom duration and JIA disease activity over time.
Main Methods:
- Retrospective cohort study of 58 children diagnosed with JIA.
- Collected data on symptom duration, pain, energy, sleep, anxiety, depression, and disease activity.
- Used Cox proportional hazards and mixed effects linear regression to analyze medication failure and disease activity.
Main Results:
- Nearly half of patients experienced initial medication failure within 9 months.
- Longer symptom duration and higher energy levels at diagnosis were protective against medication failure.
- Symptom duration showed a transient association with higher disease activity in the early post-diagnosis period.
Conclusions:
- Increased energy and prolonged symptom duration prior to diagnosis appear to protect against initial treatment failure in JIA.
- Incorporating patient-reported data into treatment decisions may enhance therapeutic success in JIA management.
Objective:
Children with juvenile idiopathic arthritis (JIA) frequently exhibit symptoms months before diagnosis. The aims of this study were to assess whether baseline patient-reported outcomes (PROs) are associated with changes in JIA pharmacotherapy treatment and whether symptom duration prior to JIA diagnosis is associated with disease activity scores over time.
Methods:
This is a retrospective cohort study of patients with an incident diagnosis of JIA. Patient-reported symptom duration, pain, energy, disease activity, sleep, anxiety, and depression screenings, as well as provider-reported disease activity and joint count, were collected during routine clinical care. Cox proportional hazards evaluated PROs, disease activity scores, and symptom duration with initial medication failure within 9 months of diagnosis. Multivariate mixed effects linear regression evaluated the association of symptom duration with disease activity scores.
Results:
There were 58 children (66% female, 35% oligoarticular JIA) in the cohort. Nearly half of patients failed initial therapy within 9 months. Unadjusted analysis showed that higher energy (hazard ratio [HR]: 0.82; 95% confidence interval [CI]: 0.69-0.99; P = 0.04) and longer symptom duration (HR: 0.96; 95% CI: 0.93-0.99; P = 0.03) at diagnosis were protective against medication failure. Adjusted analysis showed that symptom duration prior to diagnosis was protective against medication failure (HR: 0.95; 95% CI: 0.92-0.99; P = 0.02); there was no association between medication failure and pain, psychiatric symptoms, or disease activity scores. There was a positive association with longer symptom duration and higher disease activity at 30 and 60 days, but this was not sustained.
Conclusion:
Higher energy levels and longer symptom duration are protective against initial JIA treatment failures. Initial treatments informed by patient-reported data could lead to more successful outcomes by changes in treatment paradigms.
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