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The potential interaction between clopidogrel and proton pump inhibitors: a systematic review
© Lima and Brophy; licensee BioMed Central Ltd. 2010
Received: 23 September 2010
Accepted: 6 December 2010
Published: 6 December 2010
Recently, several publications have investigated a possible drug interaction between clopidogrel and proton pump inhibitors (PPIs), and regulatory agencies have issued warnings despite discordant study results. In an attempt to clarify the situation, we performed a systematic review with a critical analysis of study methodologies to determine whether varying study quality (that is, bias) could explain the discordant results.
A systematic review of all studies reporting clinical outcomes was performed using an electronic literature search of the MEDLINE and EMBASE databases, abstracts from the major cardiology conferences and a hand-search of bibliographies from identified articles. Each study was evaluated for its risk of bias according to a prespecified quality measure scale.
A total of 18 studies were identified. Ten of 13 studies judged to be of low scientific quality reported a statistically positive interaction between clopidogrel and the general class of PPIs, and each concluded this was likely a clinically meaningful effect. None of the five studies judged to be of moderate or high quality reported a statistically significant association. Multiple sources of heterogeneity (that is, different populations, outcomes assessed, drug exposure methods and study quality) prevented a formal quantitative analysis of all studies. An increased risk of bias was observed in the positive studies, resulting in an inverse correlation between study quality and a reported statistically positive interaction (10/13 versus 0/5; P = p = 0.007). There was also no clinical evidence for a positive interaction according to specific PPIs.
The observed association between clopidogrel and PPIs is found uniquely in studies judged to be of low quality and with an increased risk of bias. High-quality evidence supporting a clinically significant clopidogrel/PPI interaction is presently lacking.
Clopidogrel is a widely prescribed thienopyridine for the prevention of atherothrombotic complications following acute coronary syndromes (ACS) or percutaneous coronary interventions (PCIs) . Clopidogrel is a prodrug that has no intrinsic antiplatelet activity without activation by hepatic metabolism through the cytochrome P450 (CYP) system . Multiple CYP enzymes have been implicated in this process, but recently the CYP2C19 enzyme has assumed predominance as it is involved in both sequential oxidative steps . The possibility of drug interactions limiting clopidogrel's efficacy was raised several years following in vitro statin and clopidogrel studies, but without definitive clinical confirmation of increased adverse outcomes [4–6]. Recently, mechanistic in vitro studies have suggested that proton pump inhibitors (PPIs) may diminish clopidogrel's clinical efficacy via CYP2C19 competitive inhibition [7–10]. Consistent with these in vitro observations, several clinical studies have shown higher cardiovascular events in clopidogrel patients exposed to PPIs compared to those not exposed [11, 12], leading the Food and Drug Administration (FDA)  and the European Medicines Agency  to issue public alerts recommending the avoidance of prescribing PPIs in patients who also take clopidogrel. However, as the studies have largely been nonexperimental, the possibility of a spurious association due to bias needs to be attentively considered.
This is a clinically important question as many cardiac patients are also at high risk of gastrointestinal (GI) bleeding (due to age, smoking and concomitantly prescribed drugs), and PPIs may substantially mitigate this risk . Previous reviews of this interaction question have appeared [16–20], but they have not (1) been systematic, (2) provided a critical analysis of methodological issues or (3) integrated these safety concerns with prior knowledge of clopidogrel's time frame of action. The present review addresses these issues by performing a systematic and critical analysis of all clinical studies of this putative interaction.
We reviewed the MEDLINE and EMBASE electronic databases from January 1, 2005, to October 7, 2010, without any language restriction, combining search terms for clopidogrel ("clopidogrel" OR "Plavix" OR "thienopyridine"), PPIs ("PPI" OR " omeprazole" OR "lansoprazole" OR "pantoprazole" OR "esomeprazole" OR "rabeprazole") with those for cardiovascular outcomes ("mortality" OR "cardiovascular disease" OR "heart disease" OR "CAD" OR "MI" OR "UA" OR "coronary angiography" OR "coronary restenosis" OR "PCI" OR "stroke") and drug interaction ("interaction" OR " inhibition" OR " CYP2C19"). References of relevant identified articles were hand-searched for additional studies. Abstracts from medical organization conferences (American Heart Association, American College of Cardiology, European Society of Cardiology and Transcatheter Cardiovascular Therapeutics) were manually searched from 2005. A priori it was decided that only articles reporting clinical outcomes would be retained. Mechanistic in vitro studies measuring platelet aggregation were therefore excluded. Two investigators independently reviewed articles for inclusion and study quality. Both reviewers examined the methodology component independently of the study results, but given the publicity surrounding the individual studies it was impossible to ensure that the reviewers were totally blinded to the outcomes. It was planned to resolve disagreements by consensus, but there was perfect agreement between the investigators on their initial assessments. This systematic review was performed according to the PRISMA guidelines (see online Additional file 1).
Overall study quality was defined as high for well-performed randomized clinical trials (RCTs) as they exhibit the best internal validity. Observational studies are considered of lower quality as they have less internal validity due to numerous potential biases and consequently could attain a maximum moderate quality score. By following published guidelines to improve the reporting of observational studies  and specifically to mitigate against potential biases , we qualitatively evaluated all the observational studies for their propensity for the most common and important biases (selection, confounding and misclassification), thereby allowing their final classification into moderate- or low-quality levels. Overall observational study quality was judged to be moderate if the propensity for bias was low and specific methods to minimize bias were employed (explicit consideration of the time dependency of drug exposure and appropriate clinical outcome assessment to minimize misclassification, multiple methods to assess confounding and multivariate sensitivity analyses to test the independence and robustness of their results). Alternatively, studies were judged to be at moderate risk for bias and hence a low quality score.
The quality score of unpublished studies was systematically reduced by one grade owing to the absence of formal peer review. Isolated abstracts were considered to be of low quality as there are insufficient details to fully evaluate these reports. Finally, whenever possible, an external quality measure that compared survival curves from the clopidogrel efficacy randomized trials to the observational hazard ratios was performed to check for consistency in the etiologically relevant time windows.
Since study heterogeneity existed with respect to research methods, quality, study populations and health care systems, it was decided a priori that quantitative data pooling was inappropriate.
Propensity for bias*
Procedures to minimize bias**
(all PPIs combined)
Secondary analyses according to specific PPIs
Authors' conclusions about clopidogrel-PPI interaction
Ho et al. 
L, O, P, R
3-year mortality or ACS
OR: 1.25; 95% CI: 1.11-1.41
O = OR: 1.24; 95% CI: 1.08-1.41
R = OR, 2.83; 95% CI: 1.96-4.09
"Concomitant use after hospital discharge for ACS was associated with increased risk of adverse outcomes."
Juurlink et al. 
L, O, P, R
90-day nonfatal MI
OR: 1.27; 95% CI: 1.03-1.57
P = OR 1.02, 95% CI 0.70-1.47
Non P = OR 1.40 (1.10-1.77)
"Concomitant therapy with PPIs other than pantoprazole was associated with loss of beneficial effects of clopidogrel."
Aubert et al. 
1-year combined stroke, MI, angina or CABG
OR:1.79; 95% CI 1.62-1.97
"The drug interaction between PPIs and clopidogrel may result in serious adverse outcomes within one year of therapy initiation."
Banerjee et al. 
Mortality, MI, repeat revascularization and stroke
OR 1.54 no CI P < 0.006
"PPI(s) with clopidogrel is associated with an increased risk."
Bhatt et al. 
3,267 ACS PCI
130-day CD, nonfatal MI, revascularization or ischemic stroke
HR: 1.02; 95% CI = 0.70-1.51
Only O studied
"No apparent cardiovascular interaction between clopidogrel and omeprazole"
Dunn et al. 
1-year death, MI or stroke
OR: 1.63; 95% CI, 1.02-2.62
"PPI use was associated with an increased cardiovascular risk."
Gaspar et al. 
O, L, R
6-month death, MI or UA
8.8% vs. 8.4%, P = NS
"Was not associated with a worse prognosis in patients with ACS"
Gupta et al. 
L, O, R
4-year death, MI or TVF
OR: 1.95; 95% CI: 1.09-3.49
"PPIs may attenuate clopidogrel's beneficial antiplatelet effect."
Huang et al. 
5-year all-cause mortality
HR: 1.65; 95% CI, 1.35-2.01
"Concomitant use should be done with care to avoid adverse outcomes."
O'Donoghue et al. 
E, L, O, P, R
1-year CD, MI or stroke
OR: 0.94; 95% CI: 0.80-1.11
No specific data reported "Regardless of PPI type (including omeprazole alone or the exclusion of pantoprazole), no independent association existed"
"No clinically relevant adverse cardiovascular interaction between clopidogrel and PPIs."
Pezalla et al. 
1-year adjusted MI
OR 4.3; 95% CI 2.2-8.4#
"Evidence is pointing toward a potentially significant interaction."
Ramirez et al. 
P = 0.32
"Concomitant use of PPI's did not result in adverse cardiovascular outcomes at one year."
Rassen et al. 
18,565 ACS PCI
E, L, O, P, R
180-day death or MI
OR: 1.22; 95% CI: 0.99-1.51
O = RR 1.17; 95% CI: 0.68-2.01
P = RR 1.26; 95% CI: 0.93-1.71
"We did not observe conclusive evidence of a clopidogrel/PPI interaction."
Ray et al. 
20,596 ACS PCI
E, L, O, P, R
1-year MI, CD or stroke
HR: 0.99; 95% CI, 0.82-1.19
E = HR 0.71; 95% CI 0.48-1.06
L = HR 1.06; 95% CI 0.77-1.45
O = HR 0.79;95% CI 0.54-1.15
P = HR 1.08; 95% CI 0.88-1.32
R = HR 0.54; 95% CI 0.30-0.97
"Concurrent use of a PPI was not associated with a statistically significant increased risk for serious cardiovascular disease."
Sarafoff et al. 
30-day stent thrombosis
OR NR, P = 0.002
death OR NR, P = 0.04
"A PPI is associated with higher rates of stent thrombosis and an increased mortality."
Stockl et al. 
2,066 ACS PCI
E, L, O, P, R
1-year nonfatal MI
HR: 1.93; 95% CI: 1.05-3.54
P = HR 2.18; 95% CI 0.88-5.39
"Patients who received clopidogrel plus a PPI had a significantly higher risk."
Tsiaousis et al. 
1-year death HR: 1.1; 95% CI: 0.7-1.4
1-year MI HR: 1.0; 95% CI: 0.8-1.3
"PPIs drug therapy does not have any impact on the effectiveness."
Charlot et al. 
E, L, O, P
1-year death, MI, stroke
HR: 0.98; 95% CI, 0.88-1.10
"No difference in risk associated with the type of PPI"
"No statistically significant interaction occurred between a PPI and clopidogrel."
Among the full published studies judged to be methodologically weak, several potential biases (selection, residual confounding, immortal time and interpretative) were noted. Ten of 13 studies judged to be of low quality reported a statistically significant association for a harmful clopidogrel-PPI interaction, while none of the five moderate-quality studies found an association (P = 0.007).
Each individual study evaluated a combined exposure to any PPI for the assessment of their primary endpoint, with the exception of the experimental study , which was restricted to omeprazole. One study  did report a difference between pantoprazole and nonpantoprazole PPIs in their association with adverse clinical outcomes, but the corrected proper statistical analysis actually revealed no difference . No other study demonstrated a clinically significant difference in clinical outcomes among the different PPIs.
Our systematic review identified 18 clinical studies of a clopidogrel-PPI interaction, with the majority (10) reporting a statistically significant result. Multiple sources of heterogeneity (different populations, outcomes assessed, drug exposure methods and study quality) existed between the studies, preventing a formal quantitative analysis of all studies. However, a stratified analysis based on study quality demonstrated an inverse correlation between study quality and a positive outcome. Moreover, none of the 18 studies found a clinically meaningful difference between the various PPIs. Therefore, high-quality evidence supporting a clinically significant clopidogrel-PPI interaction is presently lacking. Consequently, while good prescribing patterns are to be endorsed for all medications, recent edicts to avoid PPIs in cardiac patients with a clinical indication for their use seem poorly justified.
It bears repeating that the only high-quality randomized trial permitting an unconfounded assessment of a causal association  did not show any evidence of harm. Moreover, it may be argued that post hoc analyses of clinical trial data offer better internal validity than other observational studies because of a greater homogeneity in the patient population, increased and higher-quality baseline clinical data and better outcome validation, thereby potentially mitigating, but certainly not eliminating, possible biases . Our evaluation of the present studies empirically confirmed this association, with the post hoc clinical trial  receiving a higher score by our independent criteria providing further external support of our quality scale. Again, this higher-quality study did not show evidence for the putative interaction.
Our systematic review provides a reproducible, prespecified and comprehensive review of the totality of the evidence in the literature of a potential interaction between clopidogrel and PPIs, thereby facilitating informed decision making. However, our systematic review may be criticized for our inability to ensure total blinding of methodological assessment from outcomes. As with any systematic review, we are also limited by the quality of the original publications. While we found a paucity of high-quality clinical evidence to support a clopidogrel-PPI interaction either collectively or individually, the power to find such an association is limited and does not preclude the possibility that later high-quality studies may appear to confirm this putative drug association.
The issue of adverse outcomes associated with concomitant use of clopidogrel and PPIs has been assessed in previous reviews [16–20], as well as by American and European regulatory agencies [13, 14], which concluded that the interaction is clinically significant. However, previous reviews have been dominated by studies with surrogate laboratory endpoints, were not systematic in identifying the clinical evidence, did not consider the putative interaction effect as a function of our previous knowledge of clopidogrel efficacy and did not provide a critical analysis of the methodological issues of each study. Lower-quality observational studies tend to overestimate effect size because of bias . In the case of regulatory agencies, the threshold to report putative clinical adverse effects is naturally low in an effort to protect public health. However, with the recent spate of controversies regarding the cardiovascular safety of approved drugs such as rofecoxib and rosiglitazone, there is perhaps a strong desire for these agencies to avoid appearing inactive and rather to be perceived as proactive. Nevertheless, it is disconcerting that the potential positive benefits of avoiding gastrointestinal bleeds in high-risk patients appear to have been minimized if not ignored and that regulatory decisions have been made not on a systematic assessment of the clinical evidence, but rather largely on surrogate laboratory data and isolated clinical studies of questionable validity. One regulatory agency  has targeted specific PPIs as being culpable without a single valid clinical study to support this claim. Correctly or not, the impression is that the safety of the regulatory agencies from criticism has become more important than the critical assessment of public health safety.
Beyond our specific conclusion that the evidence for a clinically meaningful clopidogrel-PPI interaction is poor, our critical analysis of this potential drug interaction leads to several general observations regarding pharmacoepidemiological research and subsequent policy decisions. First, selection bias or confounding by indication remains a potential threat to all observational research of both intended and unintended effects. Second, residual confounding is likely to be persistent when multivariate analysis is limited to data routinely collected from purely administrative data sets lacking the necessary clinical granularity. Post hoc analyses of randomized trials are similarly subject to the same potential biases, but the magnitude may be less owing to both a more homogeneous source population (from the strict inclusion and exclusion criteria, which favor the recruitment of populations with only one major health issue), the availability of more extensive baseline clinical data (decreasing residual confounding) and more systematic outcome assessment through adjudication (decreasing misclassification or information bias), thereby allowing a more rigorous assessment of the independent contribution of any putative association. Third, studies of surrogate endpoints (for example, platelet inhibition) may provide interesting avenues for future outcomes research, but these studies should not be used for clinical and regulatory decision making. The perils of surrogate markers have been repeatedly demonstrated in cardiovascular medicine, with specious examples ranging from ventricular ectopy suppression to lowering of glycosylated hemoglobin. Fourth, when possible, cohort studies should present survival functions, which may help in determining the reasonableness of conclusions by ensuring that events occur within the etiologically relevant time windows as demonstrated by RCTs. Finally, the time-varying nature of drug exposure must be meticulously tracked and sensitivity analyses must be performed to assess the robustness of conclusions to residual confounding or measurement error.
Readers should reasonably expect that the peer review process provides some guidance and discussion about potential biases in observational research. Too often there is a tendency to explain discordant study results not by considering biases, but by assuming that the results are due to different populations, interventions or outcomes [43, 44]. In our opinion, the probability of such effect modification is often small compared to the probability of bias. While some biases are subtle, others become more obvious with attentive reading and consideration of the totality of the evidence. The need to improve the reliability and value of medical research has been well recognized by many groups [43–45], and several guidelines have been published [21, 22], including those that pertain to observational research, but more specific guidelines for designing and interpreting pharmacoepidemiological studies may be helpful.
This systematic review of the putative drug interaction between clopidogrel and PPIs identified 18 clinical studies. Rigorous and extensive evaluation of the study methodologies demonstrated that the majority were of low quality, and only these studies reported a positive association between clopidogrel-PPI exposure and increased cardiovascular events. Supporting the notion that bias may be responsible for a spurious association, the increase in cardiovascular events attributed to this interaction appears to be occurring within a therapeutic window when clopidogrel has not been shown to be etiologically active. Conversely, all studies assessed as high quality did not demonstrate this association. No study was able to isolate any individual PPI as being more prone to adverse cardiac outcomes. Careful attention to the methodological details of published studies is therefore mandatory to avoid reaching questionable scientific conclusions. In light of this systematic review, and given the potential benefit of PPIs for patients at high risk of gastrointestinal bleeding, regulatory agencies may wish to reevaluate their recent edicts regarding this putative interaction.
This work did not benefit from any external funding. Dr Brophy is a funded research scientist of Le Fonds de la Recherche en Santé du Québec.
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