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Volume 32, Issue 4, Pages 426-432 (July 2010)


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Utility of the Beck Depression Inventory to screen for and track depression in injection drug users seeking hepatitis C treatment

Paul E. Holtzheimer, M.D., M.Sc.aCorresponding Author Informationemail addressemail address, Jason Veitengruber, M.D.b, Chia C. Wang, M.D., M.S.c, Meighan Krows, B.A.c, Hanne Thiede, D.V.M.d, Anna Wald, M.D.cef, Peter Roy-Byrne, M.D.b

Received 7 November 2009; accepted 2 February 2010. published online 05 April 2010.

Abstract 

Objective

Treating acute hepatitis C (HCV) in injection drug users (IDUs) is complicated by a high prevalence of psychiatric comorbidities that may lead to increased risk for depressive complications of interferon treatment. Effective screening strategies are needed to help non-psychiatric clinicians identify depressive disorders.

Methods

Thirty IDUs with acute HCV completed the Beck Depression Inventory (BDI), underwent a psychiatric examination, and were randomized to 24 weeks of pegylated interferon treatment (IFA) or observation (OBS). Sensitivity, specificity, positive (PPV) and negative predictive values (NPV) of the BDI for diagnosing depression (with a cutoff >10) were calculated. The psychiatrist's diagnosis was used as the gold standard. Depression severity was assessed over time with the BDI.

Results

Forty-seven percent of individuals met criteria for a depressive disorder. Sensitivity (91%) and NPV (92%) were high for the BDI; specificity (58%) and PPV (56%) were low. BDI worsened in 2 patients completing the study (one IFA, one OBS); two IFA patients were discontinued for possible depression-related complications. At baseline, subject-rated fatigue was associated with alanine aminotransferase level.

Conclusion

The BDI is an adequate tool for ruling out depressive disorders in active IDUs with acute HCV, but specificity is low. Psychiatric consultation is recommended for all active IDUs being considered for acute HCV treatment.

a Department of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, GA 30322, USA

b Department of Psychiatry and Behavioral Sciences, University of Washington School of Medicine and Harborview Medical Center, Seattle, WA 98104, USA

c Department of Medicine, University of Washington School of Medicine, Seattle, WA 98195, USA

d Public Health Seattle & King County, Seattle, WA 98104, USA

e Department of Medicine, Epidemiology and Laboratory Medicine, University of Washington School of Medicine, Seattle, WA 98195, USA

f Vaccine and Infectious Disease Institute, Fred Hutchinson Cancer Research Center, Seattle, WA 98199, USA

Corresponding Author InformationCorresponding author. Tel.: +1 404 727 9004; fax: +1 404 727 3233.

 This study was approved by the Institutional Review Boards of all participating centers. Informed consent was obtained from all study participants.

PII: S0163-8343(10)00017-4

doi:10.1016/j.genhosppsych.2010.02.001


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