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However, increased drug exposure, decreased clearance, and increased coagulation have been reported with decreased renal function.82 For patients with stage 4 CKD, in whom exposure is in

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Antithrombotic Therapy in Patients With Chronic

Kidney Disease

Davide Capodanno, MD, PhD; Dominick J Angiolillo, MD, PhD

Chronic kidney disease (CKD) is a pandemic public health

problem, with ⬎500 million people worldwide

esti-mated to have some form of kidney injury.1 Survey data

suggest that the prevalence of CKD in the United States has

increased between 1988 to 1994 and 1999 to 2004 from 10%

to 13%, reaching a rate of 14% in 2010.2,3 Overlapping

conditions such as acute kidney injury play an important role

in the growing epidemiology of CKD, and underlying CKD is

in turn an important risk factor for acute kidney injury and

end-stage renal disease Key factors contributing to the

increased prevalence of CKD include the aging population

and the growing burden of diabetes mellitus.4The prevalence

of stage 3 or 4 CKD has been reported to be⬇38% for adults

ⱖ70 years old versus ⬇1% in adults 20 to 39 years of age.2,5

Patients with diabetes mellitus are found to present with CKD

in about one third of cases, with diabetic nephropathy as the

most common cause of renal impairment.6Notably,

numer-ous epidemiological studies have shown that patients with all

stages of CKD experience higher rates of atherothrombotic

disease manifestations and processes with thromboembolic

potential such as atrial fibrillation than the general

popula-tion.7–10 This underscores the importance of antithrombotic

treatment strategies in these patients However, the

risk-to-benefit ratio with antithrombotic therapies may be altered in

CKD In fact, patients with CKD also have an increased risk

of bleeding complications.11–13 Importantly, bleeding has

emerged as an independent predictor of adverse outcomes,

including mortality.14 –17Moreover, patients with severe CKD

are less likely to receive medications of proven benefit.18,19

Overall, these findings contribute to explain why patients

with reduced renal function have poorer prognosis compared

with patients with preserved renal function

Defining the fine balance between safety and efficacy

remains a challenge in patients with CKD treated with

antithrombotic therapy Unfortunately, dosing errors, which

commonly occur in patients with CKD, accounts for almost

one third of adverse drug events, and more than half of these

errors occur at the prescription stage.20 Therefore,

under-standing whether a drug should or should not be prescribed

and individualizing dosage regimens are key to balancing the

safety and efficacy profiles of antithrombotic medications in CKD patients This article provides an overview of the currently available evidence on the use of antithrombotic therapy in patients with CKD In particular, a description of thrombosis and hemostatic profiles that characterize CKD patients, considerations for use of antithrombotic agents, including antiplatelet and anticoagulant therapies, and a review of the safety and efficacy data in CKD patients in the settings of coronary artery disease manifestations and atrial fibrillation are provided A discussion of antithrombotic therapy in patients with acute kidney injury and end-stage renal disease is beyond the scope of this article

CKD: Definitions

The Kidney Disease Outcomes Quality Initiative of the National Kidney Foundation defines CKD as either kidney damage or a decreased kidney glomerular filtration rate (GFR) of⬍60 mL 䡠 min⫺1䡠 1.73 m⫺2forⱖ3 months.21The different stages of CKD are listed in Table 1 While stages 3 through 5 are characterized by a gradient of GFR ranges, markers of structural or functional kidney damage other than GFR, including blood, urine, or imaging tests abnormalities, need to be present to establish a diagnosis of stage 1 and stage

2 CKD Kidney failure is defined as either a GFR of ⬍15

mL䡠 min⫺1䡠 1.73 m⫺2 or a need for initiation of kidney replacement therapy (dialysis or transplantation) End-stage renal disease is a US administrative definition that includes patients treated by dialysis or transplantation regardless of the GFR level Many calculators are available to estimate the GFR The National Kidney Foundation recommends using the Modification of Diet in Renal Disease equation.22

Thrombosis and Hemostasis: Biological Considerations in Patients With CKD

Patients with CKD may present with platelet dysfunction and abnormalities in the enzymatic coagulation cascade This may explain why patients with CKD may experience 2 opposite hemostatic complications: bleeding diathesis and thrombotic tendencies.23

From the University of Florida College of Medicine–Jacksonville, Jacksonville (D.C., D.J.A.), and Ferrarotto Hospital, University of Catania, Catania, Italy (D.C.).

The online-only Data Supplement is available with this article at http://circ.ahajournals.org/lookup/suppl/doi:10.1161/CIRCULATIONAHA 111.084996/-/DC1.

Correspondence to Dominick J Angiolillo, MD, PhD, University of Florida College of Medicine–Jacksonville, 655 W 8th St, Jacksonville, FL 32209 E-mail dominick.angiolillo@jax.ufl.edu

(Circulation 2012;125:2649-2661.)

© 2012 American Heart Association, Inc.

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Platelet dysfunction has been suggested to be the main

factor responsible for hemorrhagic tendencies in advanced

CKD and is likely to be multifactorial.11–13First, a defective

platelet adhesion to subendothelium caused by decreased

membrane expression of glycoprotein (GP) Ib receptors leads

to impaired platelet-vessel interactions.24 –26Second, platelets

of patients with CKD reveal an aggregation defect at least

partially attributable to decreased GPIIb/IIIa receptor

expres-sion with intrinsic dysfunction and the presence of a putative

uremic toxin that inhibits fibrinogen binding to GPIIb/

IIIa.27–29Finally, several intrinsic platelet abnormalities have

been described, including secretion defects related to

im-paired arachidonic acid release from platelet phospholipids

and a storage pool defect,30lower mean content of adenosine

diphosphate and ␤-thromboglobulin,31,32reduced sensitivity

to platelet agonists,33,34and decreased thromboxane A2

syn-thesis.35Overall, the normal platelet response to vessel wall

injury with platelet activation, recruitment, adhesion, and

aggregation (primary hemostasis) is defective, likely as a

consequence of uremic toxins present in the circulating

blood.36

On the other hand, uremic platelets may also display some

features of procoagulant activity such as increased thrombin

generation, phosphatidylserine exposure, and higher

concen-trations of von Willebrand factor11–13,37and platelet-derived

microparticles.38These microparticles are small vesicles with

procoagulant activity released by activated platelets that are

enriched with membrane receptors for coagulation factor Va

and provide a competent catalytic surface for the

prothrom-binase reaction, thereby contributing to the acceleration of

thrombin generation.38 These abnormalities, although less

characterized than functional defects contributing to the

bleeding tendency observed in uremic patients, contribute to

explain why patients with CKD may also present with a

greater propensity to platelet aggregation Importantly,

pa-tients with stage 3 to 4 CKD may present with significantly

enhanced platelet activation and aggregation as assessed by

multiple markers compared with those with stage 1 to 2 CKD,

as well as a higher prevalence of high on-aspirin and

on-clopidogrel platelet reactivity.39 – 43

As far as the enzymatic coagulation cascade is concerned,

hemostatic abnormalities consistent with a hypercoagulable

state have been widely described in patients with end-stage

renal disease on hemodialysis These plasmatic abnormalities

include increased fibrinogen, D-dimer, and prothrombin

frag-ments.44 – 46Likewise, plasma procoagulant activities of

fac-tors XII, XI, IX, VIII, VII, X, and II are significantly enhanced,47,48whereas the anticoagulant activity of protein C, protein S, and antithrombin III, plasminogen, and tissue type plasminogen activator is decreased in parallel.49 –52Dialysis may partially correct these defects but cannot totally elimi-nate them.26 The hemodialysis process itself may in fact contribute to bleeding through the chronic platelet activation induced by the interaction between blood and artificial surfaces.26

Pharmacological Issues and Dose Adjustment

in Patients With CKD

Guidelines and summaries of product characteristics drive guidance of dosing for patients with varying renal func-tion.53–56 The summaries provide the medicolegal reference for the responsibility of the manufacturer when dosing errors are investigated CKD may affect the pharmacokinetic pa-rameters of antithrombotic drugs in several ways (Table 2) A reduced renal excretion up to 50%, in particular, leads to drug accumulation in almost two thirds of patients.57In parallel, altered pharmacodynamic responses have also been de-scribed.58In this section, the mechanism of action of the most commonly prescribed antithrombotic agents, including anti-platelet and anticoagulant therapies, and how they are af-fected by reduced renal function and dosing considerations are described A summary of recommendations for dose adjustment of antithrombotic therapies in patients with CKD

is provided in Tables I and II in the online-only Data Supplement

Antiplatelet Therapies Aspirin

Aspirin selectively and irreversibly acetylates cyclooxygen-ase-1, thereby blocking the formation of thromboxane A2in platelets.59Aspirin is eliminated mainly by hepatic metabo-lism but is also excreted unchanged in the urine to an extent that depends on the dosage and urinary pH Prostaglandin-induced vasodilatation is important in maintaining renal blood flow in subjects with CKD.60By inhibiting the synthe-sis of renal prostaglandins, aspirin makes CKD patients vulnerable to further deterioration in renal function For the above reasons, the package insert recommends that aspirin should be avoided in patients with severe renal impairment.61 However, although this recommendation is followed for primary prevention, in patients with coronary artery disease manifestations, low-dose aspirin (⬍100 mg) is still used in clinical practice even in the presence of severe renal impair-ment Nonsteroidal anti-inflammatory drugs other than aspi-rin and paracetamol are associated with disease progression

Table 1 Stages of Chronic Kidney Disease

Stage Description

GFR,

mL 䡠 min ⫺1 䡠 1.73 m ⫺2

1 Kidney damage with normal or

increased GFR

⬎90

2 Mild reduction in GFR 60–89

3 Moderate reduction in GFR 30–59

4 Severe reduction in GFR 15–29

GFR indicates glomerular filtration rate Adapted from the National Kidney

Federation 21 with permission from the publisher © 2002, Elsevier BV.

Table 2 Pharmacokinetic Parameters Affected by Chronic Kidney Disease

Increased bioavailability Increased distribution Prolonged time to reach maximum drug concentration Prolonged half-life

Reduced excretion

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and should be avoided in patients with CKD owing to further

decrease in volume of renal blood flow resulting from

decreased prostaglandin synthesis and, less frequently, acute

interstitial nephritis.62

P2Y 12 Receptor Antagonists

Thienopyridines (ie, clopidogrel, prasugrel) and

cyclopentyl-triazolopyrimidines (ie, ticagrelor) are irreversible and

revers-ible inhibitors, respectively, of the platelet adenosine

diphos-phate P2Y12receptor, which is a key signaling pathway of

platelet activation Therapeutic experience with P2Y12

recep-tor antagonists is limited in patients with stage 4 to 5 CKD

The summary of product characteristics of clopidogrel

rec-ommends caution when using clopidogrel in the CKD

population.63

The pharmacokinetics of the active metabolite of prasugrel

is similar in patients with normal and in those with impaired

renal function In patients with stage 5 CKD, exposure to the

active metabolite of prasugrel is about half that of healthy

control subjects and patients with stage 3 CKD, but this issue

does not translate into significant changes in platelet

aggre-gation after ADP stimuli.64 As a result, the summary of

product characteristics of prasugrel does not recommend dose

adjustment based on renal function while warning that there

is limited experience with prasugrel in patients affected by

stage 5 CKD The metabolism and excretion of ticagrelor

depend minimally on the kidneys.65Although the mechanism

has not been elucidated, creatinine levels may increase during

treatment with ticagrelor, especially in patients⬎75 years of

age, those with stage 3 to 4 CKD at baseline, and those

receiving concomitant treatment with angiotensin receptor

blockers, warranting that creatinine levels be monitored 1

month after treatment initiation.66The summary of product

characteristics of ticagrelor does not recommend dose

adjust-ment based on renal function, but like clopidogrel and

prasugrel, use in patients with stage 5 CKD is not

recom-mended because of the lack of data in this specific

subpop-ulation The pharmacokinetics of cangrelor, the first

paren-teral P2Y12receptor antagonist not yet approved for use in

humans, is not affected by renal impairment.67 Elinogrel,

another P2Y12receptor antagonist available for intravenous

and oral administration, has a balanced renal and hepatic

clearance.68

Protease-Activated Receptor Type 1 Antagonists

There were no significant changes in the results of laboratory

tests, including kidney function, in preclinical testing of

vorapaxar and atopaxar, 2 thrombin receptor antagonists

currently under more advanced clinical testing for the

treat-ment and prevention of arterial thrombosis.69

GPIIb/IIIa Inhibitors

No dose adjustment based on renal function is required for

abciximab because of the rapid removal of free drug from the

circulation by the reticuloendothelial system.70 However,

because the potential risk of bleeding is increased in patients

with stage 4 CKD, the use of abciximab in CKD patients

should be considered only after careful appraisal of the risks

and benefits In patients with stage 3 to 4 CKD, the clearance

of eptifibatide is reduced by⬇50%, and steady-state plasma levels are approximately doubled The maintenance dose of eptifibatide should therefore be reduced from 2.0 to 1.0

␮g 䡠 kg⫺1䡠 min⫺1 in patients with creatinine clearance ⱖ30

to ⬍50 mL/min.71 Use in patients with more severe renal impairment is contraindicated Renal excretion also contrib-utes significantly to the elimination of tirofiban.72As a result,

in patients with stage 4 CKD, the infusion rate of tirofiban should be adjusted from 0.1 to 0.05␮g 䡠 kg⫺1䡠 min⫺1

Anticoagulant Therapies Indirect Thrombin Inhibitors

Unfractionated heparin is metabolized primarily in the liver and endothelium, thereby not requiring dose adjustment in stage 4 to 5 CKD.73 Conversely, enoxaparin, the most extensively studied low-molecular-weight heparin, is elimi-nated predominantly via the renal pathway Although moni-toring of anticoagulation activity and dose adjustment of enoxaparin are not required in patients with stage 2 to 3 CKD, those with stage 4 CKD experience decreased clearance of enoxaparin and drug accumulation, leading to increased half-life, drug exposure, and bleeding risk.74 As a conse-quence, guidelines recommend extending the dosing interval

of the maintenance dose of enoxaparin (1.0 mg/kg) from 12 to

24 hours in patients with stage 4 CKD presenting with an acute coronary syndrome (ACS).55 Given the concerns of overdosing, many clinicians in clinical practice consider this dose-adjusted regimen even in patients with stage 3 CKD

Direct Thrombin Inhibitors

Bivalirudin is cleared from plasma by a combination of renal mechanisms and enzymatic cleavage Because drug elimina-tion is linearly related to GFR, the infusion dose of bivaliru-din may need to be reduced in patients with advanced CKD

In particular, dose adjustment from 1.75 to 1.0 or 0.25

mg䡠 kg⫺1䡠 h⫺1should be considered in patients with stage 4

or 5 CKD, respectively.75

Parenteral Anti–Factor Xa Inhibitors

Fondaparinux is eliminated mainly as unchanged drug by the kidneys in subjects with normal kidney function.76 Con-versely, the clearance of fondaparinux decreases with in-creased renal impairment.73,77No dose reduction is required for patients with stage 2 to 3 CKD, whereas fondaparinux should be avoided in patients with stage 4 CKD.78 Otamixa-ban, another parenteral factor X inhibitor under advanced phase clinical testing, exhibits mixed renal and biliary excre-tion with constant renal clearance.79

Oral Anticoagulants: Vitamin K Antagonists and Novel Anti–Factor II and Anti–Factor X Antagonists

Warfarin and acenocoumarol (vitamin K antagonists) elimi-nation is not governed primarily by the kidneys Nonetheless, careful dosing and more frequent international normalized ratio monitoring have been recommended in patients with stage 3 CKD because of the higher baseline risk of bleeding complications.73The respective summaries of product char-acteristics contraindicate vitamin K antagonists in patients with stages 4 to 5 CKD,80although they are still often used

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judiciously in clinical practice to prevent thromboembolic

recurrences

Dabigatran is a direct thrombin inhibitor approved for

clinical use in patients with atrial fibrillation but not ACS

Elimination of dabigatran is predominantly (85%) via the

renal pathway, with⬇80% of the administered dose excreted

unchanged in the urine (Figure 1).81Limited data are

avail-able on dabigatran pharmacokinetics in patients with CKD

However, increased drug exposure, decreased clearance, and

increased coagulation have been reported with decreased

renal function.82 For patients with stage 4 CKD, in whom

exposure is increased by a factor of 6, dose adjustment to 75

mg twice daily is recommended by the Food and Drug

Administration (FDA) on the basis of pharmacokinetic and

pharmacodynamic considerations more than safety or

effi-cacy data.81However, other regulatory boards, including the

European Medicine Agency, issued a recommendation on the

110 mg twice-daily dose for use on an individual basis and at

the physician’s discretion in patients with low

thromboem-bolic and high bleeding risks.83Both the FDA and European

Medicine Agency labels of dabigatran have recently been

updated to advise physicians to assess renal function before

starting therapy and to test it annually in patients⬎75 years

of age and those with creatinine clearance⬍50 mL/min In

addition, the FDA label now states that physicians should

consider using the 75 mg twice-daily dose in patients with

creatinine clearance of 30 to 50 mL/min who are also taking

dronedarone or systemic ketoconazole The concomitant use

of dabigatran and GPIIb/IIIa inhibitors should be avoided in

patients with stage 4 CKD

Different daily doses and regimens (once or twice daily) of

rivaroxaban have been used in pivotal phase II and III trials

of atrial fibrillation (20 mg daily) and ACS (2.5–10 mg twice

daily) The approved dose of rivaroxaban for atrial fibrillation

is 20 mg once daily A dose modification from 20 to 15 mg

once daily is required in atrial fibrillation patients with

creatinine clearance⬍50 mL/min, whereas rivaroxaban is not

recommended in patients with stage 5 CKD.84Rivaroxaban is

not yet approved for ACS Other orally active direct factor Xa

inhibitors at advanced stages of clinical development include

apixaban and edoxaban, which have predominantly nonrenal

clearance and thereby represent potentially interesting

alter-natives to warfarin and other selective coagulation factor

antagonists in CKD patients (Figure 1) Similar to

rivaroxa-ban, a range of different daily doses of apixaban has been

used in pivotal trials of atrial fibrillation (5–10 mg daily) and

ACS (2.5 mg twice daily, 10 mg daily, 10 mg twice daily, 20

mg daily) Apixaban has not yet received approval for clinical

use in atrial fibrillation or ACS Betrixaban, another factor Xa

inhibitor in the early stages of development, could also be

potentially of increased advantage in CKD patients because it

is metabolized in the liver rather than being excreted by the

kidney The development of the oral anti–factor X inhibitor

darexaban has recently been discontinued after completion of

phase II clinical testing because of difficulty in finding a

commercial partner for larger phase III testing and intensified

competition in this product area.85

Impact of Antithrombotic Therapies in CKD Patients With Coronary Artery Disease Antiplatelet Therapy

Aspirin

Low-dose aspirin is as effective as higher doses in preventing ischemic events but is also associated with a lower rate of major bleeding and an improved net efficacy-to-safety bal-ance.86,87 However, even low-dose aspirin may affect renal function in elderly patients.88 –90Few primary or secondary prevention trials specifically addressed the aspirin benefit-to-risk ratio in CKD patients In the primary prevention Hyper-tension Optimal Treatment (HOT) study, low-dose aspirin therapy was associated with greater absolute reduction in major cardiovascular events and mortality in hypertensive patients with CKD than in those with normal kidney function This finding can be explained in part by the high baseline risk

of CKD patients, thereby translating a similar relative benefit into a greater absolute benefit Importantly, an increased risk

of major bleeding was outweighed by the substantial benefits, and aspirin therapy had no detrimental effect on renal function.91Among 2539 patients with type 2 diabetes mellitus and coexisting renal dysfunction enrolled in the Japanese Primary Prevention of Atherosclerosis With Aspirin for Diabetes (JPAD) trial, low-dose aspirin therapy did not reduce the primary ischemic end point in patients with stage

1 to 2 CKD compared with those with stage 3 to 4 CKD, suggesting the potential for a differential effect of low-dose aspirin therapy in diabetic patients with mild renal impair-ment.92 In an individual patient meta-analysis from the Antithrombotic Trialists’ Collaborative Group that included

105 cardiovascular events in 2704 patients with stage 5 CKD,

a 41% odds reduction in the risk of vascular death, myocar-dial infarction (MI), and stroke with antiplatelet therapy among hemodialysis patients was found compared with a 22% odds reduction seen in the overall study population, although this difference was not statistically significant.93 Overall, these findings from subgroup analyses support the design of prospective randomized clinical trials of aspirin use for the primary prevention of cardiovascular events in pa-tients with different stages of CKD

P2Y12 Receptor Antagonists

In the Clopidogrel in Unstable Angina to Prevent Recurrent Events (CURE) study, the beneficial effect of adding clopi-dogrel to standard treatment was observed in all 3 tertiles of renal function (lower tertile, ⬍64 mL/min; intermediate tertile, 64 – 81.2 mL/min; upper tertile,⬎81.2 mL/min), with

a modest absolute and relative reduction in the primary ischemic end point with clopidogrel versus placebo among patients with renal dysfunction compared with those with normal renal function, although without any significant inter-action (lower third: relative risk [RR], 0.89; 95% confidence interval [CI], 0.76 –1.05]; medium third: RR, 0.68; 95% CI,

0.56 – 0.84; upper third: RR, 0.74; 95% CI, 0.60 – 0.93; P for

interaction⫽0.11)94(Figure 2) Clopidogrel treatment signif-icantly increased the risk of minor bleeding in all tertiles of renal function The risk of major or life-threatening bleeding increased moderately with the addition of clopidogrel to

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standard treatment (lower third: RR, 1.12; 95% CI, 0.83–

1.51; medium third: RR⫽1.4; 95% CI, 0.97–2.02; upper

third: RR, 1.83; 95% CI, 1.23–2.73), but this did not appear

to be greatest in those with the lowest renal function In the

Clopidogrel for Reduction of Events During Observation

(CREDO) trial, clopidogrel versus placebo reduced the

com-posite end point of death, MI, and stroke in patients with

normal renal function, but a trend in the opposite direction

was noted in patients with stage 2 to 4 CKD.96Similarly, a

post hoc analysis of the Clopidogrel for High

Atherothrom-botic Risk and Ischemic Stabilization, Management, and

Avoidance (CHARISMA) trial suggested that clopidogrel

may even be harmful in patients with diabetic nephropathy.97 This finding could be attributable to a higher likelihood of clopidogrel resistance among patients with stage 3 to 4 CKD.38 – 42Even in CKD patients, the presence of low platelet response to clopidogrel is associated with worse outcomes,98 thus emphasizing the need for novel antiplatelet strategies with a favorable risk-to-benefit profile

Prasugrel is a new-generation thienopyridine that, because

of higher bioavailability, achieves more potent antiplatelet effects than clopidogrel The Trial to Assess Improvement in Therapeutic Outcomes by Optimizing Platelet Inhibition With Prasugrel–Thrombolysis in Myocardial Infarction 38

Figure 1 Pharmacokinetics of novel

selective oral anticoagulants Schematic overview of target, hours to Cmax, half-life, and metabolism for betrixaban, rivar-oxaban, edrivar-oxaban, apixaban, and dabigatran.

Ticagrelor

Prasugrel

15.1 17.5 -14

0.7 0.6 0.5 0.8 0.91.0 1.2

P2Y 12 Inhibitor Beer Placebo Beer

Clopidogrel

Hazard Ratio for Efficacy (95% CI) Total No of Patients

Primary Endpoint Comparator-Ref (%)

Reduction

in Risk (%)

Figure 2 Effect of P2Y12receptor antag-onists stratified by creatinine clearance Hazard ratio for efficacy (95% confidence interval [CI]) evaluated as the composite end point of cardiovascular death, myo-cardial infarction, or stroke in the Clopi-dogrel in Unstable Angina to Prevent Recurrent Events (CURE), Clopidogrel for Reduction of Events During Observation (CREDO), Trial to Assess Improvement in Therapeutic Outcomes by Optimizing Platelet Inhibition With Prasugrel (TRITON), and Platelet Inhibition and Patient Out-comes (PLATO) trials according to renal function calculated with the Cockcroft-Gault equation when not specified or the Modification of Diet in Renal Disease (MDRD) equation when indicated *A sig-nificant relative risk reduction with the

study criteria or a significant P value for

interaction between subgroups NA indi-cates not available Adapted from Mon-talescot et al 95

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(TRITON-TIMI 38) randomized study documented that,

compared with clopidogrel, prasugrel results in a 19%

reduc-tion of ischemic events in moderate to high risk ACS patients

undergoing percutaneous coronary intervention (PCI).99

Al-though in the TRITON-TIMI 38 trial this benefit was

par-tially offset by the increased risk of bleeding, the net clinical

benefit (defined as death resulting from any cause, nonfatal

MI, nonfatal stroke, and TIMI major hemorrhages) remained

in favor of prasugrel In subjects with stage 3 to 4 CKD,

prasugrel was associated with a higher absolute (2.4% versus

2.1%) and a lower relative (14% versus 20%) reduction of the

primary end point compared with subjects with normal renal

function or stage 1 to 2 CKD However, in patients with stage

3 to 4 CKD (n⫽1490), the incidence of ischemic events was

not significantly different between those taking prasugrel and

those taking clopidogrel (15.1% versus 17.5%), unlike

pa-tients with stage 1 to 2 CKD or normal renal function

(n⫽11 890; 9.0% versus 11.1%), which is likely a reflection

of the smaller number of patients with stage 3 to 4 CKD

enrolled in the trial (Figure 2)

Ticagrelor is a novel antiplatelet drug belonging to the

family of cyclopentyltriazolopyrimidines that, unlike

clopi-dogrel and prasugrel, requires a dual daily administration and

reversibly binds to the P2Y12receptor In the Platelet

Inhibi-tion and Patient Outcomes (PLATO) trial, conducted in

patients with ACS, ticagrelor reduced the primary composite

end point of cardiovascular death, MI, and stroke at 12

months compared with clopidogrel, with similar

PLATO-defined major bleedings and higher non– coronary artery

bypass grafting–related major bleedings.100About 25% of the

study population met the general definition of CKD In

subjects with stage 3 to 4 CKD (n⫽3237), ticagrelor was

associated with a higher absolute (4.7% versus 1.0%) and

relative (23% versus 10%) reduction of the primary end point

than clopidogrel compared with subjects with normal renal

function or stage 1 to 2 CKD (n⫽11 965) Consistently with

the overall PLATO population, patients with CKD

experi-enced a reduction in mortality (10.0% versus 14.0%; hazard

ratio, 0.72; 95% CI, 0.58 – 0.89).101Major bleeding rates, fatal

bleedings, and non– coronary bypass–related major bleedings

were not significantly relatively increased with ticagrelor

compared with clopidogrel in patients with stage 3 to 4 CKD

Importantly, none of the above efficacy and safety outcomes

was associated with significant interaction between CKD and

treatment, which suggests that the size effect of ticagrelor

remains of the same magnitude with or without renal

insuf-ficiency (Figure 2) However, when the more contemporary

Modification of Diet in Renal Disease formula replaces the

Cockcroft-Gault equation for the definition of CKD, a

sig-nificant P value for interaction arises for the primary end

point and mortality.101 If confirmed, these findings would

target patients with stage 3 to 4 CKD as a preferred group for

ticagrelor and conversely suggest limited added value of

ticagrelor over clopidogrel in patients without stage 3 to 4

CKD The reasons for a presumptive benefit in CKD are

puzzling because they lack physiological explanation In fact,

the clearance of ticagrelor depends minimally on renal

function; therefore, other factors (ie, play of chance,

inhibi-tion of adenosine reuptake by erythrocytes, differential

ben-efits of intensified platelet inhibition in patients with different risk profiles) may have played a role In view of the above-mentioned uncertainties, whether a causal and specific effect of ticagrelor exists in patients with stage 3 to 4 CKD needs to be further elucidated.95

GPIIb/IIIa Inhibitors

CKD would seem to identify a population of high-risk patients undergoing PCI who could be considered candidates for selective use of GPIIb/IIIa receptor inhibitors Although abciximab increases the risk of bleeding in all patients submitted to revascularization, there have been some incon-sistencies among studies concerning whether the increase in relative risk is significantly greater in patients with CKD.102–104

In pooled data from abciximab trials, however, there was no difference in the rates of all major bleeding and the 30-day primary end point of death, MI, or urgent intervention in patients with CKD between the abciximab and placebo groups.105With tirofiban, the pivotal trials evaluating efficacy and safety excluded patients with serum creatinine ⬎2.5 mg/dL Among patients with stage 2 to 3 CKD in the Platelet Receptor Inhibition in Ischemic Syndrome Management in Patients Limited by Unstable Signs and Symptoms (PRISM-PLUS), tirofiban was well tolerated and effective in reducing ischemic ACS complications, with no evidence of treatment-by– creatinine-clearance interaction.106With eptifibatide, no clinical data are available for patients with serum creatinine

⬎4.0 mg/dL In the Enhanced Suppression of the Platelet IIb/IIIa Receptor With Integrilin Therapy (ESPRIT) trial, a treatment effect of eptifibatide was noted regardless of renal function and trended toward being greater in patients with stage 2 CKD.107

Anticoagulant Therapy

Currently approved anticoagulants for treatment of patients with coronary artery disease manifestations include unfrac-tionated heparin, low-molecular-weight heparins, bivalirudin, and fondaparinux Other agents in advanced stages of clinical development include oral (dabigatran, rivaroxaban and apixa-ban) and parenteral (otamixiapixa-ban) anticoagulant agents The kidneys eliminate most of these drugs Therefore, assessment

of renal function before administration in patients receiving anticoagulants is of primary importance

A total of 11 881 patients with ACS from the Global Registry of Acute Coronary Events (GRACE) were divided into 3 groups according to creatinine clearance strata Low-molecular-weight heparin alone was more beneficial than unfractionated heparin alone, regardless of renal status Bleeding rates were significantly lower with low-molecular-weight heparin plus GPIIb/IIIa inhibitors than with unfrac-tionated heparin plus GPIIb/IIIa inhibitors.108

Bivalirudin provides comparable suppression of ischemic events with a decrease in bleeding events compared with heparin and GPIIb/IIIa inhibition.109 –111 Among 5710 pa-tients referred to PCI from the Second Randomized Evalua-tion in PCI Linking Bivalirudin to Reduced Clinical Events (REPLACE-2) study, stage 3 to 4 CKD was associated with increased ischemic events, bleeding complications, and 1-year mortality.112There was no interaction between

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ment assignment, bleeding, or ischemic complications and

stage 3 to 4 CKD In a meta-analysis of 3 randomized trials

(n⫽5035) comparing bivalirudin with heparin during PCI, the

relative benefit of bivalirudin with respect to ischemic and

bleeding events was maintained regardless of renal function

The absolute benefit in terms of ischemic and bleeding

complications increased with increasing CKD stage (normal

renal function or stage 1 CKD, 2.2%; stage 2 CKD, 5.8%;

stage 3 CKD, 7.7%; stage 4 CKD, 14.4%; P for trend⬍0.001,

P for interaction⫽0.044).113 The authors concluded that

bivalirudin provides greater absolute benefit in patients with

impaired renal function In the Acute Catheterization and

Urgent Intervention Triage Strategy (ACUITY) trial, stage 3

to 4 CKD was present in 2469 of 12 939 randomized ACS

patients (19.1%) with baseline creatinine clearance data.114

Similar to the overall population, the use of bivalirudin

monotherapy in patients with stage 3 to 4 CKD resulted in

nonstatistically different ischemic outcomes but significantly

less 30-day major bleeding compared with heparin plus a

GPIIb/IIa inhibitor No significant interaction between

treat-ment (bivalirudin or abciximab plus heparin) and renal

function (GFR⬎83 or ⱕ83 mL/min) was found in another

trial specifically focusing on patients with non–ST-segment–

elevation MI undergoing PCI with regard to the primary net

clinical outcome of death, large recurrent MI, urgent target

vessel revascularization, or major bleeding at 30 days.111In

the Harmonizing Outcomes With Revascularization and

Stents in Acute Myocardial Infarction (HORIZONS-AMI),

stage 3 to 4 CKD was present at baseline in 554 of 3397

patients (16.3%) undergoing primary PCI.115 Patients with

stage 3 to 4 CKD randomized to bivalirudin monotherapy

versus heparin plus GPIIb/IIa inhibitors had no significant

difference in major bleeding or death compared with those

without stage 3 to 4 CKD

The Fifth Organization to Assess Strategies in Acute

Ischemic Syndromes (OASIS-5) trial showed similar efficacy

of fondaparinux and enoxaparin in reducing the risk of

ischemic events at 9 days However, fondaparinux

substan-tially reduced major bleeding (2.2% versus 4.1%; odds ratio,

0.52; P⬍0.001) and 30-day mortality (2.9% versus 3.5%;

odds ratio, 0.83; P⫽0.02).116A post hoc analysis focusing on

patients with measured baseline creatinine showed that, in

patients with stage 3 to 4 CKD, the benefit of fondaparinux

compared with enoxaparin was more marked as a

conse-quence of lower bleeding rates.117

Novel anticoagulants are under clinical testing in the

setting of ACS as an adjunct to dual antiplatelet therapy In

the phase II Study of Otamixaban Versus Unfractionated

Heparin and Eptifibatide in Non-ST Elevation Acute

Coro-nary Syndrome (SEPIA-ACS-1), intermediate doses of the

new intravenous direct factor Xa inhibitor otamixaban

showed a trend toward lower ischemic end points with a

similar rate of bleeding complications compared with

unfrac-tionated heparin plus eptifibatide118; however, patients with

stage 4 to 5 CKD were excluded from this study Further

testing with otamixaban (0.08-mg/kg bolus plus infusion at

0.10 or 0.14 mg䡠 kg⫺1䡠 h⫺1) in a phase III clinical trial is

ongoing (NCT01076764) In the phase II Dose Finding Study

for Dabigatran Etexilate in Patients With Acute Coronary

Syndrome (RE-DEEM) trial, dabigatran was associated with

a dose-dependent (ranging from 50 to 150 mg twice daily) increase in bleeding events and significantly reduced coagu-lation activity in patients with a recent MI.119No significant interaction with subgroups based on creatinine clearance was noted, but patients with stage 4 to 5 CKD were not included

in the trial Phase III testing in the setting of ACS is not being pursued with dabigatran In the phase II Apixaban for Prevention of Acute Ischemic Safety Events (APPRAISE-1) trial, apixaban (2.5 to 20 mg twice daily) resulted in a dose-dependent increase in bleeding compared with placebo

in patients with a recent ACS, but a trend toward a reduction

in clinically relevant ischemic events was also noted.120 However, the phase III Apixaban for Prevention of Acute Ischemic Events 2 (APPRAISE-2) trial did not confirm these ischemic benefits using apixaban at a 5-mg twice-daily dose

In particular, the trial was stopped prematurely after recruit-ing 7392 of the planned 10 800 patients because an interim analysis showed that the increase in major bleeding with apixaban, including increases in events of fatal and intracra-nial bleeding, was not counterbalanced by the expected decrease in recurrent ischemic events compared with pla-cebo.121 The safety and tolerability of rivaroxaban at total daily doses ranging from 5 to 20 mg in patients with a recent ACS have been the objective of the phase II Rivaroxaban in Combination With Aspirin Alone or With Aspirin and a Thienopyridine in Patients With Acute Coronary Syndromes (ATLAS ACS-TIMI 46) trial.122Clinically significant bleed-ing was increased in the rivaroxaban groups in a dose-dependent manner The primary efficacy end point, a com-posite of death, MI, stroke, or severe recurrent ischemia requiring revascularization, was numerically, albeit nonsig-nificantly, lower in patients treated with rivaroxaban Rivar-oxaban doses of 2.5 and 5 mg twice daily reduced the risk of the composite end point of death resulting from cardiovascu-lar causes, MI, or stroke in the ATLAS-2 trial with no significant interaction based on CKD stage but also increased the risk of major bleeding and intracranial hemorrhage.123 Unlike APPRAISE-2, in which apixaban was tested at the same dose used for atrial fibrillation, a lower dose of rivaroxaban than that used in atrial fibrillation patients was used in the ATLAS-2, with the best benefit, including reduced mortality, observed with a 2.5 mg dose

Impact of Antithrombotic Therapies in CKD Patients With Atrial Fibrillation

CKD may be found in⬇35% of patients with atrial fibrilla-tion, with 3.3% of patients presenting with stage 4 to 5 CKD.124,125Although the efficacy of vitamin K antagonists is well established for the prevention of stroke in patients with atrial fibrillation, warfarin is widely underused, at a cost of a greater number of unnecessary disabling strokes and systemic embolisms.126This underuse is explained by a fear of causing fatal bleedings, but some shortcomings of warfarin use, including the need for international normalized ratio moni-toring and multiple environmental and genetic factors,127play another relevant role and warrant the development of novel alternatives to warfarin Importantly, cost issues are going to

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factor into the decision-making process with any new

anticoagulant

In the Randomized Evaluation of Long-Term

Anticoagu-lation Therapy (RE-LY) trial, patients were randomly

as-signed to receive 150 mg dabigatran twice daily, 110 mg

dabigatran twice daily, or warfarin titrated to achieve an

international normalized ratio of 2.0 to 3.0.128Both

dabiga-tran doses were shown to be noninferior to warfarin with

respect to the primary combined end point of stroke or

systemic embolisms, but the 150 mg regimen was

signifi-cantly superior to warfarin and the 110 mg regimen Bleeding

episodes (defined as a reduction in hemoglobin ofⱖ2 g/dL,

need for a transfusion of ⱖ2 U blood or packed cells, or

symptomatic bleeding in a critical area or organ) were less

common with dabigatran 110 mg than warfarin and were

similar between dabigatran 150 mg and warfarin Given these

findings, in October 2010, only the higher 150 mg dose

regimen of dabigatran was approved by the FDA for the

reduction of the risk of stroke and systemic embolisms in

patients with nonvalvular atrial fibrillation This decision was

affected by benefit-to-risk considerations in which disabling

stroke and systemic embolisms are given more weight than

nonfatal bleeding events.129However, because dabigatran is

cleared primarily by the kidneys (⬇80%), leading to

accu-mulation and hence potentially to more bleeding

complica-tions,130patients with CKD could theoretically benefit from a

lower dose For this reason, the FDA approved a dose of 75

mg twice daily for patients with stage 4 CKD, whereas the

European Medicine Agency currently recommends using the

lower 110 mg dose used in the RE-LY trial in patients with

low thromboembolic risk and high potential for bleeding

Analyses of the RE-LY trial restricted to patients (n⫽3343)

with creatinine clearanceⱖ30 to ⬍50 mL/min showed that

dabigatran concentrations were 2 to 3 times as high as those

in patients with normal renal function but the incidence of

stroke or systemic embolism was approximately half with

150 mg dabigatran (1.3 per 100 patient-years) compared with

110 mg (2.4 per 100 patient-years) with no significant

differences in bleeding (5.3 versus 5.7 major bleeding

epi-sodes per 100 patient-years).129Therefore, even in a

popula-tion exposed to higher dabigatran concentrapopula-tions, the

benefit-to-risk ratio is in favor of the 150 mg dose Of note, although

no relevant interaction was found between creatinine

clear-ance and the relative risk of the primary outcome with both

doses of dabigatran compared with warfarin in the RE-LY

trial, patients with stage 4 to 5 CKD were excluded.128

However, patients with stage 4 to 5 CKD are known to be at

increased risk for atrial fibrillation owing to structural and

electric atrial remodeling.131,132

In the Rivaroxaban Once-Daily Oral Direct Factor Xa

Inhibition Compared With Vitamin K Antagonism for

Pre-vention of Stroke and Embolism Trial in Atrial Fibrillation

(ROCKET-AF),⬎14 000 patients with atrial fibrillation were

randomized to 20 mg rivaroxaban once daily (or 15 mg in

patients with moderate renal impairment at screening) or to

dose-adjusted warfarin (titrated to an international

normal-ized ratio of 2.5) Rivaroxaban was found to be noninferior to

warfarin in terms of the combined primary end point of stroke

and systemic embolisms and was superior to warfarin in the

on-treatment but not in the stricter intention-to-treat analysis, raising concerns about potentially poor adherence with rivar-oxaban in real-world practice In terms of bleeding, the rates

of the composite of major and nonmajor clinically relevant bleeding were comparable in the rivaroxaban and warfarin treatment groups, with less fatal bleeding and intracranial hemorrhage observed among patients treated with rivaroxa-ban Compared with patients with creatinine clearance⬎50 mL/min, the 2950 patients (20.7%) with creatinine clearance ⱖ30 to ⬍50 mL/min enrolled in the ROCKET-AF trial were older and had higher event rates regardless of study treat-ment.133 Among patients with creatinine clearance ⱖ30 to

⬍50 mL/min, the annualized rates of the primary end point were 2.32% with rivaroxaban 15 mg once daily and 2.77% with warfarin (hazard ratio, 0.84; 95% CI, 0.57–1.23) in the per-protocol population The intention-to-treat analysis yielded similar results (hazard ratio, 0.86; 95% CI, 0.63– 1.17) Major and clinically relevant nonmajor bleeding oc-curred in 17.82% and 18.28% of patients in the rivaroxaban

and warfarin groups (P⫽0.76) After the results from the ROCKET-AF trial became available, rivaroxaban was re-cently approved by the FDA for use in the prevention of stroke and systemic embolism in patients with nonvalvular atrial fibrillation.134

In the Apixaban for the Prevention of Stroke in Subjects With Atrial Fibrillation (ARISTOTLE) trial, comparing apixaban 5 mg twice daily with warfarin in subjects with atrial fibrillation and risk factors for stroke, the oral direct factor Xa inhibitor apixaban was found to be superior to warfarin for the prevention of stroke and systemic embo-lism.135Importantly, apixaban was also associated with less bleeding and lower mortality than warfarin There was no interaction between treatment type and CKD stage for the

primary efficacy outcome (P for interaction⫽0.72) However,

a significant interaction (P⫽0.03) was found for the primary safety outcome In particular, patients with stage 3 to 4 CKD appeared to gain a larger risk reduction in major bleeding with apixaban over warfarin compared with patients with stage 1 CKD or those with no renal impairment Apixaban is currently pending approval by drug-regulating authorities for clinical use

Recommendations for Clinical Practice

Patients receiving antithrombotic medications should be screened for CKD General measures to prevent progression

of CKD, including control of contributing risk factors (ie, hypertension, diabetes mellitus) and avoidance of potentially nephrotoxic medications, such as nonsteroidal anti-inflammatory drugs, should be considered The choice and dose of antithrombotic drugs need to be carefully evaluated in patients with CKD Therefore, patients requiring aspirin therapy should opt for low-dose regimens (⬍100 mg) Pa-tients requiring a P2Y12receptor antagonist have the option

of choosing clopidogrel (ACS and non-ACS), ticagrelor (ACS), or prasugrel (only ACS undergoing PCI), none of which requires renal dosing adjustments In addition to defining the clinical setting (ACS versus non-ACS; PCI versus coronary artery bypass graft surgery versus medically managed), patients requiring P2Y12-inhibiting therapy with a

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high risk of bleeding should consider using clopidogrel since

the more potent agents prasugrel and ticagrelor are both

contraindicated in patients at high risk of bleeding If

bleed-ing risk is less of a concern and should patients require more

potent P2Y12 receptor blockade, then the choice between

prasugrel and ticagrelor may depend on the individual patient

Prasugrel is contraindicated in patients with a prior transient

ischemic attack/stroke, and should be used with caution in

patients with low weight and the elderly, and considered only

if patients underwent PCI in the setting of an ACS.56

Ticagrelor is contraindicated in patients with prior

hemor-rhagic stroke and severe hepatic impairment, and should be

used with precaution in patients treated with potent inhibitors

or inducers of CYP3A activity due to drug interactions

Although ticagrelor can be used across the spectrum of ACS,

managed both medically and invasively, its use should be

carefully considered in patients with poor compliance given

its twice-daily administration.56 Also, aspirin at a

mainte-nance dose ⬎100 mg should be avoided as this has been

associated with reduced effectiveness of ticagrelor.136

Numerous antithrombotic agents available for parenteral

use require dosage adjustments in patients with CKD, which

clinicians should be aware of in order to avoid overdosing,

and include eptifibatide, tirofiban, bivalirudin, enoxaparin,

and fondaparinux For ACS patients undergoing PCI in whom

potent antithrombotic effects are warranted, recent trial data

are strongly supportive of the use of bivalirudin, which,

compared with GPIIb/IIIa inhibitors, has a similar impact on

ischemic events but with significantly less bleeding, making

bivalirudin a more desirable agent in this setting However, if

a GPII/IIIa inhibitor is chosen, it is important to ensure that

dosage adjustments occur in CKD patients when

small-molecule GPIIb/IIIa inhibitors (eptifibatide, tirofiban) are

used Long-term oral anticoagulation with warfarin requires

careful dosing and more frequent international normalized

ratio monitoring in CKD patients The development of novel

antithrombotic agents with a more favorable safety profile

may have a promising role in this ever-growing population,

but more clinical experience with these agents is warranted

before we will be able to define which of them may have a

better niche for patients with CKD

Conclusions

CKD is a frequent consequence of diabetes mellitus, renal

disease, or aging Safety with antithrombotic therapy is a

major concern, especially in patients with renal impairment,

because of the potential for increased risk of bleeding events

Therefore, understanding strategies of antithrombotic

man-agement in patients with CKD is of key importance The lack

of studies performed specifically in patients with impaired

renal function, particularly those with acute kidney injury or

end-stage renal disease, who are generally excluded from

many large-scale clinical trials, often leads to either no

recommendation on their most appropriate antithrombotic

treatment regimen or sometimes arbitrary assumptions

Over-all, the choice and combination of antithrombotic drugs used

should be balanced against the individual risk of thrombotic

and bleeding complications Clinical experience with newer

agents is still limited, and more data from large-scale clinical

trials or even dedicated studies in patients with CKD are warranted

Disclosures

Dr Angiolillo reports receiving honoraria for lectures from Bristol Myers Squibb, Sanofi-Aventis, Eli Lilly Co, Daiichi Sankyo, Inc, Abbott Vascular, and AstraZeneca; consulting fees from Bristol Myers Squibb, Sanofi-Aventis, Eli Lilly Co, Daiichi Sankyo, Inc, The Medicines Company, Portola, Novartis, Medicure, Accumetrics, Arena Pharmaceuticals, Abbott Vascular, AstraZeneca, Merck, and Evolva; and research grants from Bristol Myers Squibb, Sanofi-Aventis, GlaxoSmithKline, Otsuka, Eli Lilly Co, Daiichi Sankyo, Inc, The Medicines Company, Portola, Accumetrics, Schering-Plough, AstraZeneca, and Eisai Dr Capodanno has received hono-raria for lectures from AstraZeneca and Eli Lilly Co.

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