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Famotidine adjunctive pharmacotherapy for schizophrenia: preliminary data
S I Deutsch1, R B Rosse, K A Kendrick
1Department of Veterans Affairs Medical Center, Psychiatry Service, Washington, DC 20422, USA.
Clinical Neuropharmacology
|December 1, 1993
Summary
Famotidine, an H2 antagonist, showed modest benefits as an add-on treatment for schizophrenia, improving specific symptoms. Further research with placebo controls is recommended to confirm famotidine
Area of Science:
- Psychiatry
- Pharmacology
Background:
- Idiopathic psychotic disorders, such as schizophrenia and schizoaffective disorder, often require adjunctive treatments for improved outcomes.
- Histamine-2 (H2) receptor antagonists are primarily used for acid reflux but may have unexplored neurological applications.
- Treatment resistance and frequent hospitalizations are significant challenges in managing schizophrenia.
Purpose of the Study:
- To investigate the efficacy of famotidine as an adjunct to conventional antipsychotic therapy in patients with idiopathic psychotic disorders.
- To assess the impact of famotidine on overall psychiatric symptoms and negative symptoms in schizophrenia patients.
Main Methods:
- An open-label study involving 10 treatment-refractory patients with schizophrenia or schizoaffective disorder.
- Famotidine (20 mg twice daily) was added to existing antipsychotic regimens for 3 weeks.
- Symptom severity was assessed using the Brief Psychiatric Rating Scale (BPRS) and the Schedule for the Assessment of Negative Symptoms (SANS).
Main Results:
- Significant reductions in total BPRS and Clinical Global Impression scores were observed during famotidine treatment.
- Improvements were primarily noted in specific symptom subscales of the BPRS, not negative symptoms (SANS).
- The magnitude of symptom improvement was generally small, despite statistical significance.
Conclusions:
- Famotidine may offer a potential adjunctive benefit for specific symptoms in some schizophrenia patients.
- Larger, double-blind, placebo-controlled trials with higher famotidine doses are warranted.
- Exploring other H2 receptor antagonists with enhanced blood-brain barrier penetration could be beneficial.