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Pharmacological interventions for self-harm in adults

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Pharmacological interventions for self-harm in adults

Sübutlu məlumatların xülasələri
15.07.2015 • Sonuncu dəyişiklik 15.07.2015
Editors

The evidence is insufficient to reach firm conclusions regarding pharmacological interventions in self harm patients.

A Cochrane review included 7 studies witha total of 546 participants. Of the 6 trials that reported information on gender, the majority of participants were female (63.5%). The trials included investigated the effectiveness of various pharmacological agents: mianserin, nomifensine, paroxetine, antipsychotics, lithium and natural products (omega-3 essential fatty acid; n-3EFA). The patients had had an episode of self harm within 6 months. We found no significant treatment effect on repetition of self harm for newer generation antidepressants (OR 0.76, 95% CI 0.42 to 1.36; 3 trials, n=243), low-dose fluphenazine (OR 1.51, 95% CI 0.50 to 4.58; one trial, n=53), mood stabilisers (OR 0.99, 95% CI 0.33 to 2.95; one trial, n=167), or natural products (OR 1.33, 95% CI 0.38 to 4.62; one trial, n=49). A significant reduction in self harm repetition was found in a single trial of the antipsychotic flupenthixol (OR 0.09, 95% CI 0.02 to 0.50; one trial, n=30). No data on adverse effects, other than the planned outcomes relating to suicidal behaviour, were reported.

Comment: The quality of evidence is downgraded by study quality (unclear allocation concealment), inconsistency (heterogeneity in treatments) and imprecise results (few trials for each comparison).

Ədəbiyyat

  1. Hawton K, Witt KG, Taylor Salisbury TL et al. Pharmacological interventions for self-harm in adults. Cochrane Database Syst Rev 2015;7():CD011777.