Close Banner
Section Free  - CAP Smart Takes

05. Efficacy of Risperidone as Treatment for Anorexia Nervosa

Published on February 1, 2024 Certification expiration date: February 2, 2027

David R. Rosenberg, M.D.

Chair of the Department of Psychiatry & Behavioral Neuroscience - Wayne State University School of Medicine

Key Points

  • Anorexia nervosa is the deadliest psychiatric disorder and currently has no FDA-approved medication for youth.
  • Risperidone was well-tolerated but showed no efficacy, with only a 9.5% retention rate after 1 year.

Free Downloads for Offline Access

  • Free Download Audio File (MP3)

Text version

Greetings; this is David Rosenberg from the Psychopharmacology Institute. In this CAP—or Child and Adolescent Psychiatry—Smart Take, we aim to examine the role of risperidone in the treatment of children and adolescents diagnosed with anorexia nervosa. This area warrants attention; anorexia nervosa is the deadliest psychiatric disorder, with a mortality rate surpassing those of schizophrenia and other mental health conditions. This fact underscores the urgent need for improved treatment strategies. Alarmingly, there are currently no FDA-approved medications specifically for anorexia nervosa in youth—an issue that necessitates further research in order to manage this disorder better. Indeed, anorexia nervosa often proves challenging to treat, with relapse being more common than recovery. Early-onset anorexia nervosa may also have a bleak prognosis and outcome, substantiating the need for exploring alternative treatment options in this demographic.

This observational naturalistic study evaluated 120 patients diagnosed with anorexia nervosa—42 of whom were treated with risperidone over an average span of 116 days. The medication was generally well-tolerated; only 1 case reported nausea and asthenia. Unfortunately, despite its tolerability, the study’s results were disappointing. There were no significant differences between children and adolescents treated with risperidone vs those who were untreated in terms of admission or discharge rates, improvements in body mass index, or any psychopathology measures. The patient retention rate for risperidone after 3 months was 50%; after 1 year, it dropped to 9.5%. The drug was primarily discontinued due to the resolution of target symptoms. However, rehospitalization rates at 12 months were comparable between children and adolescents who were treated with risperidone and those who were not.

Despite these outcomes, it is noteworthy that this is the most extensive sample size covered in the existing literature, highlighting the need for longitudinal assessments and studies to evaluate long-term prognostic factors and tolerability. Furthermore, a comparison with broader samples is necessary; only 42 patients in this study received risperidone treatment. Other variables—such as additional treatments and behavioral therapies, comorbidities, duration of illness, the onset of illness, associated physical conditions, and illness severity—must also be considered. Although this study emphasizes risperidone’s tolerability, it fails to confirm its efficacy, raising more questions than answers.

The study is the first to assess the use of risperidone in hospitalized children and adolescents suffering from anorexia nervosa. It also prompts queries about the actual efficacy of risperidone—a drug commonly employed for various conditions, including eating disorders, in child and adolescent psychiatry. The anorexia nervosa subtype is particularly intriguing given that atypical antipsychotics like risperidone frequently result in significant weight gain—a side effect generally avoided but potentially beneficial for anorexia nervosa patients. Nevertheless, it is crucial to remember that second-generation antipsychotics are associated with carbohydrate metabolic abnormalities; although weight gain might benefit anorexia nervosa patients, exposing them to a heightened risk of metabolic syndromes, carbohydrate abnormalities, or diabetes would be detrimental.

In conclusion, although risperidone appears relatively safe and well-tolerated in children and adolescents diagnosed with anorexia nervosa—as per this particular study—it does not demonstrate any significant difference or improvement in weight gain, psychopathology measures, or rehospitalization rates. Consequently, recommending risperidone as a potent or effective medication for this population remains questionable unless future longitudinal and prospective studies successfully identify subpopulations or potential predictors of treatment response (or lack thereof) and long-term safety analysis alongside the risk of other side effects associated with these medications—particularly metabolic abnormalities.

Abstract

The Role of Risperidone in the Treatment of Children and Adolescents With Anorexia Nervosa

Jacopo Pruccoli, Luca Bergonzini, Ilaria Pettenuzzo, Antonia Parmeggiani

Background: Current Diagnostic and Statistical Manual of Mental Disorders (DSM)-5-based research provides limited data on the use of risperidone on children and adolescents with anorexia nervosa (AN) mainly in small-sample/case report studies.

Aim: To report the use of risperidone in a group of children and adolescents with feeding and eating disorders, specifically with AN.

Methods: Observational, naturalistic study. Psychopathology was assessed with Eating Disorders Inventory-3, Beck’s Depression Inventory-II, and Symptom Checklist-90-R. Data were reported for the whole sample, for patients treated with risperidone, and finally compared between patients with AN treated with risperidone and those receiving no atypical antipsychotics. Potential differences in admission-discharge changes in body mass index (BMI) and psychopathology were assessed with analyses of covariance corrected for baseline measures. Kaplan-Meier analyses were conducted to assess retention rates of risperidone (at 3 months and 1 year) and rates of rehospitalization on 1-year follow-up.

Results: The study enrolled 120 patients with AN (42 treated with risperidone). Risperidone was used for 116.7 (±122.8) days (total exposure = 3979 days) and well-tolerated (nausea, asthenia in one case). No significantly different admission-discharge improvements for BMI or psychopathology were documented for patients treated with risperidone. Risperidone showed a 3-month retention rate of 50.0% (1 year: 9.5%) and was discontinued mainly for the resolution of target symptoms. Cumulative freedom from rehospitalization at 12 months was comparable for treated and untreated patients (hazard ratio = 1.088; Log-rank p = 0.908).

Conclusions: This study reports real-life evidence of the use of risperidone in AN children and adolescents in the widest described sample so far. Longitudinal research should assess long-term prognostic factors and tolerability.

Free Files
Success!
Check your inbox, we sent you all the materials there.

Reference

Pruccoli, J., Bergonzini, L., Pettenuzzo, I., & Parmeggiani, A. (2023). The role of risperidone in the treatment of children and adolescents with anorexia nervosaJournal of Psychopharmacology, 37(6), 545-553.

Table of Contents

Learning Objectives:

  1. Analyze the effectiveness of escitalopram in treating generalized anxiety disorder in children and adolescents.
  2. Recognize that altered sleep architecture was a potential dose-dependent result of vortioxetine treatment in adolescents with MDD.
  3. Understand the uses of long-acting injectable aripiprazole lauroxil in child and adolescent psychiatry.
  4. Analyze the potential benefits of esketamine in treating adolescent MDD.
  5. Evaluate the tolerability and efficacy of risperidone as a treatment for anorexia nervosa.

Original Release Date: February 1, 2024

Review and Re-release Date: March 1, 2024

Expiration Date: February 1, 2027

Experts: David Rosenberg, M.D.

Medical Editor: Lorena Rodriguez, M.D.

Relevant Financial Disclosures: 

None of the faculty, planners, and reviewers for this educational activity have relevant financial relationships to disclose during the last 24 months with ineligible companies whose primary business is producing, marketing, selling, re-selling, or distributing healthcare products used by or on patients.

Contact Information: For questions regarding the content or access to this activity, contact us at support@psychopharmacologyinstitute.com

Instructions for Participation and Credit:

Participants must complete the activity online during the valid credit period that is noted above.

Follow these steps to earn CME credit:

  1. View the required educational content provided on this course page.

  2. Complete the Post Activity Evaluation for providing the necessary feedback for continuing accreditation purposes and for the development of future activities. NOTE: Completing the Post Activity Evaluation after the quiz is required to receive the earned credit.

  3. Download your certificate.

Accreditation Statement

This activity has been planned and implemented in accordance with the accreditation requirements and policies of the Accreditation Council for Continuing Medical Education through the joint providership of Medical Academy LLC and the Psychopharmacology Institute. Medical Academy is accredited by the ACCME to provide continuing medical education for physicians

Credit Designation Statement

Medical Academy designates this enduring activity for a maximum of 0.5 AMA PRA Category 1 credit(s)™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.

Free Files
Success!
Check your inbox, we sent you all the materials there.
Continue in the website
Instant access modal

Become a Silver, Gold, Silver extended or Gold extended Member.

2025–26 Psychopharmacology CME Program

Unlock up to 155 CME Credits, including 40 SA CME Credits.