Literature DB >> 29985565

Prescribing Trends in US Active Duty Service Members With Posttraumatic Stress Disorder: A Population-Based Study From 2007-2013.

George Loeffler1,2,3, Rachael Coller2, LaRee Tracy4, Berg Roy Derderian5.   

Abstract

OBJECTIVE: The US Veterans Affairs (VA)/Department of Defense (DoD) Posttraumatic Stress Disorder (PTSD) Clinical Practice Guidelines provide evidence-based pharmacologic treatment recommendations. Selective serotonin reuptake inhibitors (SSRIs) and serotonin-norepinephrine reuptake inhibitors (SNRIs) are considered first-line medications. Benzodiazepines are relatively contraindicated with a warning that they may cause harm. This population-based study is the first to describe prescribing patterns for active duty service members (ADSMs) diagnosed with PTSD.
METHODS: Health-care-related administrative DoD data from federal fiscal years 2007 through 2013 identified ADSMs with PTSD using ICD-9 codes. Prescription frequencies for antidepressants, benzodiazepines, antipsychotics, anticonvulsants, and other psychotropic medications were calculated for each year.
RESULTS: Between 2007 and 2013, ADSMs with a PTSD diagnosis increased from 16,931 to 70,942. SSRI or SNRI prescribing decreased from 55.4% in 2007 to 41.8% in 2010 before increasing to 54.9% in 2013. Benzodiazepine prescribing was stable between 20.9% and 22.3% through 2010 before increasing to 24.7% by 2013. Antipsychotic prescribing declined from 22.6% in 2007 to 14.6% in 2013, driven by a decrease in low-dose quetiapine (≤ 300 mg/d) prescribing, which declined from 19.1% in 2007 to 8.2% in 2013.
CONCLUSIONS: The increase in SSRI or SNRI prescribing after 2010 and the overall increase in prazosin and decrease in low-dose quetiapine prescribing all suggest increased concordance with the VA/DoD PTSD Clinical Practice Guidelines. The decline in SSRI prescribing up to 2010 is not concordant. The increase in benzodiazepine prescribing, a trend opposite that observed in the VA, is concerning. © Copyright 2018 Physicians Postgraduate Press, Inc.

Entities:  

Mesh:

Year:  2018        PMID: 29985565     DOI: 10.4088/JCP.17m11667

Source DB:  PubMed          Journal:  J Clin Psychiatry        ISSN: 0160-6689            Impact factor:   4.384


  4 in total

1.  Blocking the orexin system following therapeutic exposure promoted between session habituation, but not PTSD symptom reduction.

Authors:  Ihori Kobayashi; Thomas A Mellman; Ashley Cannon; Imani Brown; Linda Boadi; Mary Katherine Howell; Pewu Lavela; Ishaan Sandhu
Journal:  J Psychiatr Res       Date:  2021-12-14       Impact factor: 5.250

2.  Increased Prevalence of Metabolic Syndrome in Veterans with PTSD Untreated with Antipsychotic Medications.

Authors:  Barton W Palmer; Catherine Shir; Hang Chang; Mallory Mulvaney; Joshua M H Hall; I-Wei Shu; Hua Jin; James B Lohr
Journal:  Int J Ment Health       Date:  2021-08-25

3.  The role of the GABAA receptor Alpha 1 subunit in the ventral hippocampus in stress resilience.

Authors:  Z Ardi; A Richter-Levin; L Xu; X Cao; H Volkmer; O Stork; G Richter-Levin
Journal:  Sci Rep       Date:  2019-09-18       Impact factor: 4.379

4.  Effects of chronic prazosin, an alpha-1 adrenergic antagonist, on anxiety-like behavior and cortisol levels in a chronic unpredictable stress model in zebrafish (Danio rerio).

Authors:  Michael P O'Daniel; Maureen L Petrunich-Rutherford
Journal:  PeerJ       Date:  2020-01-31       Impact factor: 2.984

  4 in total

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