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Lithium treatment in children and adolescents with anorexia nervosa: clinical use, side effects and tolerability. | LitMetric

Lithium treatment in children and adolescents with anorexia nervosa: clinical use, side effects and tolerability.

Riv Psichiatr

IRCCS Istituto delle Scienze Neurologiche di Bologna, Centro Regionale per i Disturbi della Nutrizione e dell'Alimentazione in Età Evolutiva, UO Neuropsichiatria dell'Età Pediatrica, Bologna, Italy - Department of Medical and Surgical Sciences (DIMEC), University of Bologna, Italy.

Published: July 2022

AI Article Synopsis

  • Current guidelines caution against using lithium for treating Anorexia Nervosa (AN) due to possible toxicity and limited clinical evidence, particularly in children and adolescents.
  • A case series involving 7 young female patients showed that lithium was administered to improve mood, compliance with nutrition programs, and manage psychomotor agitation, with doses ranging from 171.4 to 600 mg/day.
  • Despite some adverse reactions in two patients, all experienced symptom improvement, suggesting a need for further investigation in larger, controlled studies.

Article Abstract

Purpose: Current guidelines, due to potential toxicity and lack of clinical evidence, do not recommend the use of lithium in the treatment of Anorexia Nervosa (AN). Scarce evidence is available on the use, side effects, and tolerability of this drug in children and adolescents with AN, a population characterized by specific clinical, metabolic, and hydro-electrolytic balance features. Here we report a case series of children and adolescents hospitalized for AN and treated with lithium.

Methods: Case series reporting the use of lithium in 7 female young patients with AN. Reasons for introduction, dosages, formulation, plas-ma levels, adverse drug reactions (ADR) and modifi-cations of electrocardiogram (EKG) and plasma levels of glucose, cholesterol, creatinine, urea, sodium, and thyroid-stimulating hormone (TSH) were assessed. Re-sults. Reasons for the introduction of lithium included unstable mood, insufficient compliance with nutri-tional programs, and psychomotor agitation. In all of the patients an improvement on target symptoms was observed. Lithium was started at 171.4 (+/-56.7) mg/day, up to 600.0 (+/-173.2) mg/day. The most frequent scheme was three times daily. The mean plasmatic concentration was 0.6 (+/-0.3) mmol/L at one month. One pa-tient experienced polyuria, polydipsia and dry mouth, and another showed increased creatinine kinase. No major modifications of EKG, glucose, cholesterol, cre-atinine, urea, sodium emerged.

Conclusions: In this sample of children and adolescents hospitalized for AN, lithium was administered to improve psychiatric symptoms impairing compliance. All the patients experienced an improvement on these symptoms after being admin-istered lithium. ADR were reported in 2 cases. These data should be investigated in wider populations and controlled studies.

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Source
http://dx.doi.org/10.1708/3855.38385DOI Listing

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