Skip to main content
Full access
Letters to the Editor
Published Online: 1 October 2015

Response to Stankiewicz et al.

To the Editor: In our clinical trial (1), we found that soldiers who received brief cognitive-behavioral therapy (CBT) were significantly less likely to make a suicide attempt during the 2-year follow-up period compared with soldiers who received treatment as usual (hazard ratio=0.38, 95% CI=0.16–0.87, p=0.02). In response to Stankiewicz and colleagues, we provide the results of several post hoc sensitivity analyses to address questions about nonspecific effects of individual therapy.
As recommended by these authors, we first stratified participants into two subgroups according to the total number of individual therapy sessions during the first 3 months: those attending <12 sessions and those attending ≥12 sessions. The estimated suicide attempt–free probability among those attending <12 individual therapy sessions was 95.8% in treatment as usual compared with 100% in brief CBT at 6 months, and was 73.7% in treatment as usual compared with 100% in brief CBT at 24 months. Among those attending ≥12 sessions, the attempt-free probability was 83.3% in treatment as usual compared with 94.3% in brief CBT at 6 months, and was 57.2% in treatment as usual compared with 81.3% in brief CBT at 24 months.
We next used the Cox proportional hazards model, with treatment group entered as the predictor and total number of therapy sessions during the first 3 months entered as the covariate. Overall, brief CBT was associated with significantly decreased risk for suicide attempt (hazard ratio=0.37, 95% CI=0.16–0.81, p=0.02). Separate regressions were then conducted for each stratum. Because of the absence of suicide-attempt cases among participants in brief CBT who attended <12 sessions, a Firth correction was applied. When adjusting for individual therapy attendance during the first 3 months, the magnitudes of effect by strata were comparable to our initial results: <12 sessions: hazard ratio=0.27, 95% CI=0.00–2.75, p=0.48; ≥12 sessions: hazard ratio=0.35, 95% CI=0.14–0.88, p=0.03.
Participants were next stratified into quartiles according to the number of individual therapy sessions attended during the entire follow-up (i.e., 0–12, 13–24, 25–48, and 49+ sessions). The estimated attempt-free probabilities at 6 months and at 24 months are displayed in Table 1 by treatment group. When adjusting for the total number of individual sessions attended during follow-up, brief CBT continued to be associated with significantly reduced risk for suicide attempt (hazard ratio=0.39, 95% CI=0.16–0.87, p=0.03). Adjusted results by strata favored brief CBT in all cases, though there was insufficient power to detect statistically significant differences: 1st quartile: hazard ratio=0.10, 95% CI=0.00–1.10, p=0.188; 2nd quartile: hazard ratio=0.27, 95% CI=0.05–1.14, p=0.111; 3rd quartile: hazard ratio=0.91, 95% CI=0.19–4.37, p=0.912; 4th quartile: hazard ratio=0.39, 95% CI=0.08–1.56, p=0.228.
Table 1. Estimated Suicide Attempt–Free Probabilities at 6 Months and at 24 Months by Treatment and by Total Number of Individual Therapy Sessions Attended During Follow-Up
Individual Therapy Sessions (N)Brief CBTTreatment as Usual
6 months  
 0–12100.090.4
 13–2488.569.2
 25–4887.188.9
 49+95.092.9
24 months  
 0–12100.074.5
 13–2488.561.5
 25–4879.179.0
 49+81.449.0
Overall, results of these post hoc analyses suggest the effects of brief CBT on the likelihood of follow-up suicide attempts remain reasonably stable even when accounting for the nonspecific effect of individual therapy dose. It is difficult to elucidate treatment effects given the overall study N, but the enduring impact of a brief treatment for suicidal behavior raises interesting questions regarding the unique, effective elements of care.

Reference

1.
Rudd MD, Bryan CJ, Wertenberger EG, et al: Brief cognitive-behavioral therapy effects on post-treatment suicide attempts in a military sample: results of a randomized clinical trial with 2-year follow-up. Am J Psychiatry 2015; 172:441–449

Information & Authors

Information

Published In

Go to American Journal of Psychiatry
Go to American Journal of Psychiatry
American Journal of Psychiatry
Pages: 1022 - 1023
PubMed: 26423483

History

Accepted: July 2015
Published online: 1 October 2015
Published in print: October 01, 2015

Authors

Affiliations

Craig J. Bryan, Psy.D., A.B.P.P.
From the National Center for Veterans Studies, University of Utah, Salt Lake City; and the National Center for Veterans Studies, University of Memphis, Memphis.
M. David Rudd, Ph.D., A.B.P.P.
From the National Center for Veterans Studies, University of Utah, Salt Lake City; and the National Center for Veterans Studies, University of Memphis, Memphis.

Funding Information

The authors’ disclosures accompany the original article.

Metrics & Citations

Metrics

Citations

Export Citations

If you have the appropriate software installed, you can download article citation data to the citation manager of your choice. Simply select your manager software from the list below and click Download.

For more information or tips please see 'Downloading to a citation manager' in the Help menu.

Format
Citation style
Style
Copy to clipboard

There are no citations for this item

View Options

View options

PDF/ePub

View PDF/ePub

Get Access

Login options

Already a subscriber? Access your subscription through your login credentials or your institution for full access to this article.

Personal login Institutional Login Open Athens login
Purchase Options

Purchase this article to access the full text.

PPV Articles - American Journal of Psychiatry

PPV Articles - American Journal of Psychiatry

Not a subscriber?

Subscribe Now / Learn More

PsychiatryOnline subscription options offer access to the DSM-5-TR® library, books, journals, CME, and patient resources. This all-in-one virtual library provides psychiatrists and mental health professionals with key resources for diagnosis, treatment, research, and professional development.

Need more help? PsychiatryOnline Customer Service may be reached by emailing [email protected] or by calling 800-368-5777 (in the U.S.) or 703-907-7322 (outside the U.S.).

Media

Figures

Other

Tables

Share

Share

Share article link

Share