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Use of antipsychotics and benzodiazepines in patients with psychiatric emergencies: Results of an observational trial
BACKGROUND: Conventional antipsychotics augmented with benzodiazepines have been the standard acute treatment for psychiatric emergencies for more than 50 years. The inability of patients to give informed consent limits randomised, controlled studies. This observational study on immediate therapy fo...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2507712/ https://www.ncbi.nlm.nih.gov/pubmed/18647402 http://dx.doi.org/10.1186/1471-244X-8-61 |
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author | Wilhelm, Stefan Schacht, Alexander Wagner, Thomas |
author_facet | Wilhelm, Stefan Schacht, Alexander Wagner, Thomas |
author_sort | Wilhelm, Stefan |
collection | PubMed |
description | BACKGROUND: Conventional antipsychotics augmented with benzodiazepines have been the standard acute treatment for psychiatric emergencies for more than 50 years. The inability of patients to give informed consent limits randomised, controlled studies. This observational study on immediate therapy for aggression and impulse control in acutely agitated patients (IMPULSE) evaluated the short-term effectiveness and tolerability of atypical and typical antipsychotic medications (AP) in a non-interventional setting. METHODS: This was a comparative, non-randomised, prospective, open-label, observational study. Treatment over the first 5 days was classified according to whether any olanzapine, risperidone, or haloperidol was included or not. Documentations (PANSS-excited component, CGI-aggression, CGI-suicidality, tranquilisation score) were at baseline (day 1) and days 2–6 after start of AP. RESULTS: During the short treatment-period, PANSS-EC and CGI-aggression scores improved in all cohorts. 68.7% of patients treated with olanzapine, 72.2% of patients treated with risperidone, and 83.3% of patients treated with haloperidol received concomitant benzodiazepines (haloperidol vs. non-haloperidol: p < 0.001). More patients treated with olanzapine (73.8%) were fully alert according to a tranquilisation score and active at day 2 than patients treated with risperidone (57.1%) or haloperidol (58.0%). CONCLUSION: Current medication practices for immediate aggression control are effective with positive results present within a few days. In this study, concomitant benzodiazepine use was significantly more frequent in patients receiving haloperidol. |
format | Text |
id | pubmed-2507712 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-25077122008-08-12 Use of antipsychotics and benzodiazepines in patients with psychiatric emergencies: Results of an observational trial Wilhelm, Stefan Schacht, Alexander Wagner, Thomas BMC Psychiatry Research Article BACKGROUND: Conventional antipsychotics augmented with benzodiazepines have been the standard acute treatment for psychiatric emergencies for more than 50 years. The inability of patients to give informed consent limits randomised, controlled studies. This observational study on immediate therapy for aggression and impulse control in acutely agitated patients (IMPULSE) evaluated the short-term effectiveness and tolerability of atypical and typical antipsychotic medications (AP) in a non-interventional setting. METHODS: This was a comparative, non-randomised, prospective, open-label, observational study. Treatment over the first 5 days was classified according to whether any olanzapine, risperidone, or haloperidol was included or not. Documentations (PANSS-excited component, CGI-aggression, CGI-suicidality, tranquilisation score) were at baseline (day 1) and days 2–6 after start of AP. RESULTS: During the short treatment-period, PANSS-EC and CGI-aggression scores improved in all cohorts. 68.7% of patients treated with olanzapine, 72.2% of patients treated with risperidone, and 83.3% of patients treated with haloperidol received concomitant benzodiazepines (haloperidol vs. non-haloperidol: p < 0.001). More patients treated with olanzapine (73.8%) were fully alert according to a tranquilisation score and active at day 2 than patients treated with risperidone (57.1%) or haloperidol (58.0%). CONCLUSION: Current medication practices for immediate aggression control are effective with positive results present within a few days. In this study, concomitant benzodiazepine use was significantly more frequent in patients receiving haloperidol. BioMed Central 2008-07-22 /pmc/articles/PMC2507712/ /pubmed/18647402 http://dx.doi.org/10.1186/1471-244X-8-61 Text en Copyright © 2008 Wilhelm et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Wilhelm, Stefan Schacht, Alexander Wagner, Thomas Use of antipsychotics and benzodiazepines in patients with psychiatric emergencies: Results of an observational trial |
title | Use of antipsychotics and benzodiazepines in patients with psychiatric emergencies: Results of an observational trial |
title_full | Use of antipsychotics and benzodiazepines in patients with psychiatric emergencies: Results of an observational trial |
title_fullStr | Use of antipsychotics and benzodiazepines in patients with psychiatric emergencies: Results of an observational trial |
title_full_unstemmed | Use of antipsychotics and benzodiazepines in patients with psychiatric emergencies: Results of an observational trial |
title_short | Use of antipsychotics and benzodiazepines in patients with psychiatric emergencies: Results of an observational trial |
title_sort | use of antipsychotics and benzodiazepines in patients with psychiatric emergencies: results of an observational trial |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2507712/ https://www.ncbi.nlm.nih.gov/pubmed/18647402 http://dx.doi.org/10.1186/1471-244X-8-61 |
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