Z Gastroenterol 2009; 47 - P4_31
DOI: 10.1055/s-0029-1191950

Es-Citalopram for the prevention of PEG-IFN-α and Ribavirin associated depression in HCV-infected patients without psychiatric risk factors (CIPPAD-study)

M Schäfer 1, R Sarkar 1, U Spengler 2, T Schlaepfer 3, J Ockenga 4, A Friebe 1, S Effenberger 1, L Heinze 1, P Buggisch 5, J Reimer 6, R Link 7, B Hintsche 8, V Weich 9, F van Boemmel 9, S Zeuzem 10, T Berg 9
  • 1Klinik für Psychiatrie und Psychotherapie, Campus Charité Mitte, Charité – Universitätsmedizin Berlin
  • 2Abteilung für Innere Medizin, Universitätsklinik Bonn
  • 3Klinik für Psychiatrie und Psychotherapie, Medizinische Universitätsklinik Bonn
  • 4Zentrum Innere Medizin, Klinikum Bremen Mitte
  • 5Medizinische Klinik I, UKE Hamburg
  • 6Klinik für Psychiatrie und Psychotherapie, UKE Hamburg
  • 7Medizinische Klinik, St. Josefsklinik, Offenburg
  • 8Praxis für Gastroenterologie
  • 9Klinik für Gastroenterologie und Hepatologie, Charité Campus Virchow, Charité – Universitätsmedizin Berlin
  • 10Medizinische Universitätsklinik Frankfurt

Objective: The „EsCItalopram for the Prevention of PEGASYSΘ Associated Depression study“ (CIPPAD-study) is a prospective multicentre, randomized, double-blind, placebo-controlled clinical trial with the primary objective to evaluate the impact of a 2-week antidepressant pretreatment with Escitalopram on the incidence and severity of interferon-alpha associated depression. Study design: Patients without any history of psychiatric or substance abuse disorder either received escitalopram 10mg/day 2 weeks prior to commencement of HCV therapy and or received placebo. All patients were treated with pegylated interferon-alpha-2a (PEG-IFN-α-2a) plus ribavirin. The frequency and severity of depressive episodes were defined according to DSM-IV criteria for a „major depression“ and by using the Montgomery Asperg Depression Scale (MADRS). Results: According to preliminary data from 189 patients highly significantly more patients in the placebo group (48.9%) were diagnosed from clinicians as having a major depressive episode if compared to the verum group (p<0.001). Evaluation of the severity of depressive syndromes by MADRS-scores showed that significantly more patients in the placebo group reached moderate to severe depressive symptoms during antiviral treatment (34.7%) if compared to the verum group (p=0.004). Patients in the placebo group had a 2.6 fold increased risk to reach MADRS depression scores over 15 (OR=2.57). Significantly more patients in the placebo group needed an antidepressive rescue medication with mirtazapine (p=0.004). So far no significant differences between both groups were found regarding genotype distribution and sustained virological response. Discussion: Our preliminary results clearly indicate that an antidepressive pre-treatment with escitalopram was able to significantly reduce the frequency and severity of depressive episodes during antiviral therapy with PEG-IFN-a-2a in patients without psychiatric risk factors.