Treatments and Outcomes Among Patients with Sydenham Chorea

Author:

Eyre Michael12,Thomas Terrence3,Ferrarin Emanuela4,Khamis Sonia2,Zuberi Sameer M.56,Sie Adrian67,Newlove-Delgado Tamsin8,Morton Michael6,Molteni Erika9,Dale Russell C.10,Lim Ming112,Nosadini Margherita1213, ,Aty-Marzouk Pakinam A14,Cardoso Francisco14,Cavalcanti André14,Galloway Yvonne14,Jack Susan14,Maia Debora14,Marino Achille14,Orsini Alessandro14,Sartori Stefano14

Affiliation:

1. School of Biomedical Engineering and Imaging Sciences, King’s College London, London, United Kingdom

2. Children’s Neurosciences, Evelina London Children’s Hospital at Guy’s and St Thomas’ NHS Foundation Trust, London, United Kingdom

3. Department of Paediatrics, Neurology Service, KK Women’s and Children’s Hospital, Singapore

4. Centro di Riferimento Oncologico di Aviano IRCCS, Aviano, Italy

5. Paediatric Neurosciences Research Group, Royal Hospital for Children, Glasgow, United Kingdom

6. Institute of Health and Wellbeing, University of Glasgow, Glasgow, United Kingdom

7. NHS Lanarkshire, Bothwell, United Kingdom

8. Children and Young People’s Mental Health (ChYMe) Research Collaboration, University of Exeter Medical School, Exeter, United Kingdom

9. School of Biomedical Engineering and Imaging Sciences, King’s College London, United Kingdom

10. Kids Neuroscience Centre, The Children’s Hospital at Westmead, Faculty of Medicine and Health, University of Sydney, Westmead, Australia

11. Faculty of Life Sciences and Medicine, King’s College London, United Kingdom

12. Paediatric Neurology and Neurophysiology Unit, Department of Women’s and Children’s Health, University Hospital of Padova, Padova, Italy

13. Neuroimmunology Group, Paediatric Research Institute “Città della Speranza,” Padova, Italy

14. for the Sydenham’s Chorea Systematic Literature Review Working Group

Abstract

ImportanceSydenham chorea is the most common acquired chorea of childhood worldwide; however, treatment is limited by a lack of high-quality evidence.ObjectivesTo evaluate historical changes in the clinical characteristics of Sydenham chorea and identify clinical and treatment factors at disease onset associated with chorea duration, relapsing disease course, and functional outcome.Data SourcesThe systematic search for this meta-analysis was conducted in PubMed, Embase, CINAHL, Cochrane Library, and LILACS databases and registers of clinical trials from inception to November 1, 2022 (search terms: [Sydenham OR Sydenham’s OR rheumatic OR minor] AND chorea).Study SelectionPublished articles that included patients with a final diagnosis of Sydenham chorea (in selected languages).Data Extraction and SynthesisThis study followed the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) reporting guideline. Individual patient data on clinical characteristics, treatments, chorea duration, relapse, and final outcome were extracted. Data from patients in the modern era (1945 through 2022) were entered into multivariable models and stratified by corticosteroid duration for survival analysis of chorea duration.Main Outcomes and MeasuresThe planned study outcomes were chorea duration at onset, monophasic course (absence of relapse after ≥24 months), and functional outcome (poor: modified Rankin Scale score 2-6 or persisting chorea, psychiatric, or behavioral symptoms at final follow-up after ≥6 months; good: modified Rankin Scale score 0-1 and no chorea, psychiatric, or behavioral symptoms at final follow-up).ResultsIn total, 1479 patients were included (from 307 articles), 1325 since 1945 (median [IQR] age at onset, 10 [8-13] years; 875 of 1272 female [68.8%]). Immunotherapy was associated with shorter chorea duration (hazard ratio for chorea resolution, 1.51 [95% CI, 1.05-2.19]; P = .03). The median chorea duration in patients receiving 1 or more months of corticosteroids was 1.2 months (95% CI, 1.2-2.0) vs 2.8 months (95% CI, 2.0-3.0) for patients receiving none (P = .004). Treatment factors associated with monophasic disease course were antibiotics (odds ratio [OR] for relapse, 0.28 [95% CI, 0.09-0.85]; P = .02), corticosteroids (OR, 0.32 [95% CI, 0.15-0.67]; P = .003), and sodium valproate (OR, 0.33 [95% CI, 0.15-0.71]; P = .004). Patients receiving at least 1 month of corticosteroids had significantly lower odds of relapsing course (OR, 0.10 [95% CI, 0.04-0.25]; P < .001). No treatment factor was associated with good functional outcome.Conclusions and RelevanceIn this meta-analysis of treatments and outcomes in patients with Sydenham chorea, immunotherapy, in particular corticosteroid treatment, was associated with faster resolution of chorea. Antibiotics, corticosteroids and sodium valproate were associated with a monophasic disease course. This synthesis of retrospective data should support the development of evidence-based treatment guidelines for patients with Sydenham chorea.

Publisher

American Medical Association (AMA)

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