BJPsych Open. 2016 Sep 09;2(5):286-293. doi: 10.1192/bjpo.bp.115.002451. eCollection 2016 Sep.
Initiation of pharmacotherapy for post-traumatic stress disorder among veterans from Iraq and Afghanistan: a dimensional, symptom cluster approach.
BJPsych open
Ilan Harpaz-Rotem, Robert Rosenheck, Somaia Mohamed, Robert Pietrzak, Rani Hoff
Affiliations
Affiliations
- , PhD, VACHS, The National Center for PTSD, Department of Veterans Affairs, West Haven, CT; VACHS, The Northeast Program Evaluation Center (NEPEC), Department of Veterans Affairs, West Haven, CT; Department of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.
- , MD, VACHS, VISN1 Mental Illness Research and Clinical Center (MIRECC), Department of Veterans Affairs, West Haven, CT; Department of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.
- , MD PhD, VACHS, The Northeast Program Evaluation Center (NEPEC), Department of Veterans Affairs, West Haven, CT; Department of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.
- , MPH PhD, VACHS, The National Center for PTSD, Department of Veterans Affairs, West Haven, CT; Department of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.
- , MPH PhD, VACHS, The National Center for PTSD, Department of Veterans Affairs, West Haven, CT; VACHS, The Northeast Program Evaluation Center (NEPEC), Department of Veterans Affairs, West Haven, CT; Department of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.
PMID: 27703791
PMCID: PMC5016711 DOI: 10.1192/bjpo.bp.115.002451
Abstract
BACKGROUND: The pharmacological treatment of post-traumatic stress disorder (PTSD) is extremely challenging, as no specific agent has been developed exclusively to treat this disorder. Thus, there are growing concerns among the public, providers and consumers associated with its use as the efficacy of some agents is still in question.
AIMS: We applied a dimensional and symptom cluster-based approach to better understand how the heterogeneous phenotypic presentation of PTSD may relate to the initiation of pharmacotherapy for PTSD initial episode.
METHOD: US veterans who served in the conflicts in Iraq and Afghanistan and received an initial PTSD diagnosis at the US Veterans Health Administration between 2008 and 2011 were included in this study. Veterans were followed for 365 days from initial PTSD diagnosis to identify initiation for antidepressants, anxiolytics/sedatives/hypnotics, antipsychotics and prazosin. Multivariable analyses were used to assess the relationship between the severity of unique PTSD symptom clusters and receiving prescriptions from each medication class, as well as the time from diagnosis to first prescription.
RESULTS: Increased severity of emotional numbing symptoms was independently associated with the prescription of antidepressants, and they were prescribed after a substantially shorter period of time than other medications. Anxiolytics/sedatives/hypnotics prescription was associated with heightened re-experiencing symptoms and sleep difficulties. Antipsychotics were associated with elevated re-experiencing and numbing symptoms and prazosin with reported nightmares.
CONCLUSIONS: Prescribing practices for military-related PTSD appear to follow US VA/DoD clinical guidelines. Results of this study suggest that a novel dimensional and symptom cluster-based approach to classifying the phenotypic presentation of military-related PTSD symptoms may help inform prescribing patterns for PTSD.
DECLARATION OF INTEREST: None.
COPYRIGHT AND USAGE: © The Royal College of Psychiatrists 2016. This is an open access article distributed under the terms of the Creative Commons Non-Commercial, No Derivatives (CC BY-NC-ND) license.
References
- J Psychiatr Res. 2014 Feb;49:31-6 - PubMed
- Hum Psychopharmacol. 2012 Jul;27(4):386-91 - PubMed
- J Psychopharmacol. 2015 Mar;29(3):264-9 - PubMed
- J Nerv Ment Dis. 2014 Feb;202(2):97-104 - PubMed
- Am J Psychiatry. 2013 Sep;170(9):1003-10 - PubMed
- Arch Intern Med. 2007 Mar 12;167(5):476-82 - PubMed
- Psychiatr Serv. 2008 Oct;59(10):1184-90 - PubMed
- N Engl J Med. 2004 Jul 1;351(1):13-22 - PubMed
- CNS Drugs. 2009;23(1):19-34 - PubMed
- J Clin Psychiatry. 2013 Dec;74(12):1241-8 - PubMed
- Int Clin Psychopharmacol. 2003 Jan;18(1):1-8 - PubMed
- J Psychiatr Res. 2012 Mar;46(3):317-22 - PubMed
- Biol Psychiatry. 2008 Mar 15;63(6):629-32 - PubMed
- Br J Psychiatry. 2015 Feb;206(2):93-100 - PubMed
- J Anxiety Disord. 2009 Oct;23(7):995-1001 - PubMed
- Biol Psychiatry. 2007 Apr 15;61(8):928-34 - PubMed
- JAMA. 2007 Nov 14;298(18):2141-8 - PubMed
- Aust N Z J Psychiatry. 2007 Aug;41(8):637-48 - PubMed
- JAMA. 2006 Mar 1;295(9):1023-32 - PubMed
- Biol Psychiatry. 2006 Apr 1;59(7):577-81 - PubMed
- Psychiatr Serv. 2011 Jan;62(1):22-7 - PubMed
- Am J Psychiatry. 2016 Dec 1;173(12 ):1205-1212 - PubMed
- JAMA. 2011 Aug 3;306(5):493-502 - PubMed
- Am J Psychiatry. 2014 Jan;171(1):117 - PubMed
- Am J Psychiatry. 2010 Jul;167(7):748-51 - PubMed
- J Clin Psychiatry. 2008 Jun;69(6):959-65 - PubMed
- Psychiatr Serv. 2013 Feb 1;64(2):149-55 - PubMed
- Am J Psychiatry. 2003 Feb;160(2):371-3 - PubMed
- Br J Psychiatry. 2010 Oct;197(4):326-7 - PubMed
- J Clin Psychiatry. 2002 Jul;63(7):565-8 - PubMed
- Psychiatr Serv. 2009 Sep;60(9):1175-81 - PubMed
- Arch Gen Psychiatry. 2009 Apr;66(4):417-21 - PubMed
- Cochrane Database Syst Rev. 2006 Jan 25;(1):CD002795 - PubMed
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