Proton pump inhibitors may enhance the risk of citalopram- and escitalopram-associated sudden cardiac death among patients receiving hemodialysis

被引:8
作者
Assimon, Magdalene M. [1 ]
Pun, Patrick H. [2 ,3 ]
Al-Khatib, Sana M. [3 ,4 ]
Brookhart, M. Alan [5 ]
Gaynes, Bradley N. [6 ,7 ]
Winkelmayer, Wolfgang C. [8 ]
Flythe, Jennifer E. [1 ,9 ]
机构
[1] Univ N Carolina, Kidney Ctr, Div Nephrol & Hypertens, Dept Med,UNC Sch Med, Chapel Hill, NC 27599 USA
[2] Duke Univ, Sch Med, Dept Med, Div Nephrol, Durham, NC 27706 USA
[3] Duke Clin Res Inst, Durham, NC USA
[4] Duke Univ, Med Ctr, Div Cardiol, Durham, NC 27710 USA
[5] Duke Univ, Sch Med, Dept Populat Hlth Sci, Durham, NC USA
[6] UNC Sch Med, Dept Psychiat, Chapel Hill, NC USA
[7] UNC Gillings Sch Global Publ Hlth, Dept Epidemiol, Chapel Hill, NC USA
[8] Baylor Coll Med, Selzman Inst Kidney Hlth, Sect Nephrol, Houston, TX 77030 USA
[9] Univ N Carolina, Cecil G Sheps Ctr Hlth Serv Res, Chapel Hill, NC 27599 USA
基金
美国国家卫生研究院;
关键词
citalopram; escitalopram; hemodialysis; proton pump inhibitor; sudden cardiac death; USRDS; SEROTONIN REUPTAKE INHIBITORS; OMEPRAZOLE; SAFETY; METABOLISM; NEPHROLOGY; FAILURE; FOCUS;
D O I
10.1002/pds.5428
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Purpose Polypharmacy is common in the hemodialysis population and increases the likelihood that patients will be exposed to clinically significant drug-drug interactions. Concurrent use of proton pump inhibitors (PPIs) with citalopram or escitalopram may potentiate the QT-prolonging effects of these selective serotonin reuptake inhibitors through pharmacodynamic and/or pharmacokinetic interactions. Methods We conducted a retrospective cohort study using data from the U.S. Renal Data System (2007-2017) and a new-user design to examine the differential risk of sudden cardiac death (SCD) associated with citalopram/escitalopram initiation vs. sertraline initiation in the presence and absence of PPI use among adults receiving hemodialysis. We studied 72 559 patients:14 983 (21%) citalopram/escitalopram initiators using a PPI; 26 503 (36%) citalopram/escitalopram initiators not using a PPI;10 779 (15%) sertraline initiators using a PPI; and 20 294 (28%) sertraline initiators not using a PPI (referent). The outcome of interest was 1-year SCD. We used inverse probability of treatment weighted survival models to estimate weighted hazard ratios (HRs) and 95% confidence intervals (CIs). Results Compared with sertraline initiators not using a PPI, citalopram/escitalopram initiators using a PPI had the numerically highest risk of SCD (HR [95% CI] = 1.31 [1.11-1.54]), followed by citalopram/escitalopram initiators not using a PPI (HR [95% CI] = 1.22 [1.06-1.41]). Sertraline initiators using a PPI had a similar risk of SCD compared with those not using a PPI (HR [95% CI] = 1.03 [0.85-1.26]). Conclusions Existing PPI use may elevate the risk of SCD associated with citalopram or escitalopram initiation among hemodialysis patients.
引用
收藏
页码:670 / 679
页数:10
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