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European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society · 2021

A nationwide study on Sydenham's chorea: Clinical features, treatment and prognostic factors.

СтатьяНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
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Orsini Alessandro, Foiadelli Thomas, Magistrali Mariasole, Carli Niccolò, Bagnasco Irene, Dassi Patrizia, Verrotti Alberto, Marcotulli Daniele, Canavese Carlotta, Nicita Francesco, Capuano Alessandro, Marra Chiara, Fetta Anna, Nosadini Margherita, Sartori Stefano, Papa Amanda, Viri Maurizio, Greco Filippo, Pavone Piero, Simonini Gabriele, Matricardi Sara, Siquilini Sabrina, Marchese Francesca, De Grandis Elisa, Brunenghi Bernadette Marrè, Malattia Clara, Bassanese Francesco, Bergonzini Patrizia, Bonuccelli Alice, Consolini Rita, Marseglia Gian Luigi, Peroni Diego, Striano Pasquale, Cordelli Duccio, Savasta Salvatore

Аннотация

OBJECTIVES: Sydenham's Chorea (SC) is a neuropsychiatric disorder and a major manifestation of acute rheumatic fever. The erroneous assumption that SC is a benign and self-limiting disease, has led to a lack of high-quality scientific evidence of the therapeutical and prognostic features of SC.

STUDY DESIGN: We retrospectively analyzed the medical records of patients <18-years old with SC in 17 Italian pediatric centers. Recorded data included clinical, instrumental and laboratory parameters. Prognostic risk factors including treatment regimens were assessed with univariate and multivariate sub-analysis.

RESULTS: We included 171 patients with SC. 66% had generalized chorea, and 34% hemichorea. 81% had carditis (subclinical in 65%). Additional neurological symptoms were reported in 60% of the patients, mainly dysarthria and dysgraphia. 51% had neuropsychiatric symptoms at onset, which persisted after 12 months in 10%. Among psychiatric manifestations, the most common was anxiety disorder/depression (77%). Neurological remission was reached by 93% of the patients at 6 months; 9% relapsed. Patients were treated as follows: 11% penicillin alone, 37% immunomodulatory therapy, 16% symptomatic drugs (i.e. anti-seizure medication, dopamine antagonists) and 37% both symptomatic and immunomodulatory treatment. Neurological outcome did not differ between groups. Patients receiving symptomatic drugs had a higher risk of relapse on multivariate analysis (p = 0.045).

CONCLUSIONS: Treatment of SC was largely heterogeneous. Based on our results, immunomodulatory therapy did not show higher efficacy at medium term, although it was associated to a slightly lower risk of relapse compared to symptomatic therapy. Longitudinal studies are needed to assess specific risk factors and best treatment options.

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