6533b85afe1ef96bd12b96e0

RESEARCH PRODUCT

Early Improvement and Serum Concentrations of Citalopram to Predict Antidepressant Drug Response of Patients with Major Depression

M. FricA DragivevicStefanie WagnerM. L. RaoK BolandE Ostad HajiMatthias J. MüllerAndré TadićC HiemkeG. Laux

subject

Malemedicine.medical_specialtyCitalopramCitalopramSensitivity and SpecificityPredictive Value of TestsRating scaleInternal medicinemedicineHumansPharmacology (medical)Depression (differential diagnoses)Depressive Disorder MajorReceiver operating characteristicGeneral MedicineOdds ratioMiddle AgedAntidepressive AgentsClinical trialPsychiatry and Mental healthAnesthesiaAntidepressantFemalePsychologyPsychopathologymedicine.drug

description

Post hoc analyses of clinical trials have shown that early improvement around day 14 is highly predictive for later response. More- over, evidence has been given that suffi ciently high concentrations of antidepressant drugs in blood are required to attain response. In this study, we determined cut-off levels for citalo- pram serum concentrations and clinical improve- ment during the early phase of treatment to predict later response and the predictive power of these measures either alone or in combination. Methods: Inpatients with depressive disorder according to ICD-10 who received citalopram were included. Psychopathology was assessed by the 17-item Hamilton Depression (HAMD-17) rating scale, and serum concentrations of citalo- pram were measured in weekly intervals. Results: The analysis included 55 inpatients. Receiver operating characteristics analysis revealed for citalopram a serum concentration of 53 ng/ml on day 7 and a clinical improvement of 24 % on the HAMD-17 scale on day 14 as signifi - cant cut-off values to predict response after 5 weeks of treatment. Both measures taken together predicted response on week 5 with 73 % sensitivity and 85 % specifi city with an odds ratio of 14.6. Discussion: It is concluded that treatment with citalopram should be guided by symptom rating at baseline and on day 14 and serum concentra- tion determination on day 7.

https://doi.org/10.1055/s-0033-1354370