TY - JOUR
T1 - Prognosis in heart failure and the value of {beta}-blockers are altered by the use of antidepressants and depend on the type of antidepressants used
AU - Fosbøl, Emil Loldrup
AU - Gislason, Gunnar H
AU - Poulsen, Henrik Enghusen
AU - Hansen, Morten Lock
AU - Folke, Fredrik
AU - Schramm, Tina Ken
AU - Olesen, Jonas Bjerring
AU - Bretler, Ditte-Marie
AU - Abildstrøm, Steen Z
AU - Sørensen, Rikke
AU - Hvelplund, Anders
AU - Køber, Lars
AU - Torp-Pedersen, Christian
AU - Fosbøl, Emil Loldrup
AU - Gislason, Gunnar H
AU - Poulsen, Henrik Enghusen
AU - Hansen, Morten Lock
AU - Folke, Fredrik
AU - Schramm, Tina Ken
AU - Olesen, Jonas Bjerring
AU - Bretler, Ditte-Marie
AU - Abildstrøm, Steen Z
AU - Sørensen, Rikke
AU - Hvelplund, Anders
AU - Køber, Lars
AU - Torp-Pedersen, Christian
N1 - Keywords: Adrenergic beta-Antagonists; Aged; Aged, 80 and over; Antidepressive Agents, Tricyclic; Cohort Studies; Denmark; Depression; Drug Interactions; Female; Heart Failure; Hospitalization; Humans; Kaplan-Meiers Estimate; Male; Medication Adherence; Middle Aged; Proportional Hazards Models; Registries; Risk Assessment; Risk Factors; Serotonin Uptake Inhibitors; Time Factors; Treatment Outcome
PY - 2009
Y1 - 2009
N2 - BACKGROUND: Depression worsens the prognosis in patients with cardiac disease, and treatment with antidepressants may improve survival. Guidelines recommend use of selective serotonin reuptake inhibitors (SSRIs), but knowledge of the prognostic effect of different classes of antidepressants is sparse. METHODS AND RESULTS: We studied 99 335 patients surviving first hospitalization for heart failure (HF) from 1997 to 2005. Use of HF medication and antidepressants (divided into tricyclic antidepressants [TCA] and SSRI) was determined by prescription claims. Risk of overall and cardiovascular death associated with antidepressants, HF medication, and coadministration of these 2 drug classes was estimated by Cox proportional hazard analyses. Propensity adjusted models were performed as sensitivity analysis. During the study period, there were 53 988 deaths, of which 83.0% were due to cardiovascular causes (median follow-up, 1.9 years; 5, 95% fractiles, 0.04 to 7.06 years). Use of beta-blockers was associated with decreased risk of cardiovascular death (hazard ratio [HR], 0.77; 95% CI, 0.75 to 0.79). Antidepressants were prescribed to 19 411 patients, and both TCA and SSRI were associated with increased risk of overall and cardiovascular death (TCA: HR, 1.33; CI, 1.26 to 1.40; and HR, 1.25; CI, 1.17 to 1.32; SSRI: HR, 1.37; CI, 1.34 to 1.40; and HR, 1.34; CI, 1.30 to 1.38, respectively). Coadministration of SSRI and beta-blockers was associated with a higher risk of overall and cardiovascular death compared with coadministration of beta-blockers and TCA (P for interaction <0.01). CONCLUSIONS: Use of antidepressants in patients with HF was associated with worse prognosis. Coadministration of SSRIs and beta-blockers was associated with increased risk of overall death and cardiovascular death compared with coadministration of TCAs and beta-blockers. To further clarify this, clinical trials testing the optimal antidepressant strategy in patients with HF are warranted.
AB - BACKGROUND: Depression worsens the prognosis in patients with cardiac disease, and treatment with antidepressants may improve survival. Guidelines recommend use of selective serotonin reuptake inhibitors (SSRIs), but knowledge of the prognostic effect of different classes of antidepressants is sparse. METHODS AND RESULTS: We studied 99 335 patients surviving first hospitalization for heart failure (HF) from 1997 to 2005. Use of HF medication and antidepressants (divided into tricyclic antidepressants [TCA] and SSRI) was determined by prescription claims. Risk of overall and cardiovascular death associated with antidepressants, HF medication, and coadministration of these 2 drug classes was estimated by Cox proportional hazard analyses. Propensity adjusted models were performed as sensitivity analysis. During the study period, there were 53 988 deaths, of which 83.0% were due to cardiovascular causes (median follow-up, 1.9 years; 5, 95% fractiles, 0.04 to 7.06 years). Use of beta-blockers was associated with decreased risk of cardiovascular death (hazard ratio [HR], 0.77; 95% CI, 0.75 to 0.79). Antidepressants were prescribed to 19 411 patients, and both TCA and SSRI were associated with increased risk of overall and cardiovascular death (TCA: HR, 1.33; CI, 1.26 to 1.40; and HR, 1.25; CI, 1.17 to 1.32; SSRI: HR, 1.37; CI, 1.34 to 1.40; and HR, 1.34; CI, 1.30 to 1.38, respectively). Coadministration of SSRI and beta-blockers was associated with a higher risk of overall and cardiovascular death compared with coadministration of beta-blockers and TCA (P for interaction <0.01). CONCLUSIONS: Use of antidepressants in patients with HF was associated with worse prognosis. Coadministration of SSRIs and beta-blockers was associated with increased risk of overall death and cardiovascular death compared with coadministration of TCAs and beta-blockers. To further clarify this, clinical trials testing the optimal antidepressant strategy in patients with HF are warranted.
U2 - 10.1161/CIRCHEARTFAILURE.109.851246
DO - 10.1161/CIRCHEARTFAILURE.109.851246
M3 - Journal article
C2 - 19919983
VL - 2
SP - 582
EP - 590
JO - Circulation: Heart Failure
JF - Circulation: Heart Failure
SN - 1941-3289
IS - 6
ER -