Use of antipsychotics and benzodiazepines in patients with psychiatric emergencies Results of an observational trial 英文参考文献.docVIP
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Use of antipsychotics and benzodiazepines in patients with psychiatric emergencies Results of an observational trial 英文参考文献
BMC Psychiatry
BioMedCentral
Research article
Open Access
Use of antipsychotics and benzodiazepines in patients with
psychiatric emergencies: Results of an observational trial
Stefan Wilhelm*, Alexander Schacht? and Thomas Wagner?
Address: Medical Department, Lilly Deutschland GmbH, Saalburgstra?e 153, Bad Homburg, Germany
Email: Stefan Wilhelm* - wilhelm_stefan@; Alexander Schacht - schacht_alexander@; Thomas Wagner - wagnertt@
* Corresponding author ?Equal contributors
Published: 22 July 2008
Received: 23 February 2007
Accepted: 22 July 2008
BMC Psychiatry 2008, 8:61
doi:10.1186/1471-244X-8-61
This article is available from: /1471-244X/8/61
? 2008 Wilhelm et al; licensee BioMed Central Ltd.
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (/licenses/by/2.0),
which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract
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
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