GUIDELINE

The management of antithrombotic agents for patients

undergoing GI endoscopy
Prepared by: ASGE STANDARDS OF PRACTICE COMMITTEE
Ruben D. Acosta, MD, Neena S. Abraham, MD, MSCE, FASGE (invited content expert, ad-hoc member),
Vinay Chandrasekhara, MD, Krishnavel V. Chathadi, MD, Dayna S. Early, MD, FASGE,
Mohamad A. Eloubeidi, MD, MHS, FASGE, John A. Evans, MD, Ashley L. Faulx, MD, FASGE,
Deborah A. Fisher, MD, MHS, FASGE, Lisa Fonkalsrud, BSN, RN, CGRN, Joo Ha Hwang, MD, PhD, FASGE,
Mouen A. Khashab, MD, Jenifer R. Lightdale, MD, MPH, FASGE, V. Raman Muthusamy, MD, FASGE,
Shabana F. Pasha, MD, John R. Saltzman, MD, FASGE, Aasma Shaukat, MD, MPH, FASGE,
Amandeep K. Shergill, MD, Amy Wang, MD, Brooks D. Cash, MD, FASGE, previous Committee Chair,
John M. DeWitt, MD, FASGE, Chair
This document was reviewed and approved by the Governing Board of the American Society for Gastrointestinal
Endoscopy.

This is one of a series of statements discussing the use of

GI endoscopy in common clinical situations. The Standards of Practice Committee of the American Society for
Gastrointestinal Endoscopy (ASGE) prepared this text. In
preparing this guideline, a search of the medical literature was performed using PubMed and the Cochrane
Database, with dates of search from August 1966 to
December 2014. Additional references were obtained
from the bibliographies of the identied articles and
from recommendations of expert consultants. When
limited or no data exist from well-designed prospective
trials, emphasis is given to results from large series and
reports from recognized experts. Guidelines for appropriate use of endoscopy are based on a critical review
of the available data and expert consensus at the time
the guidelines are drafted. Further controlled clinical
studies may be needed to clarify aspects of this guideline.
This guideline may be revised as necessary to account for
changes in technology, new data, or other aspects of clinical practice. The recommendations were based on reviewed studies and were graded on the strength of the
supporting evidence (Table 1).1
This guideline is intended to be an educational device
to provide information that may assist endoscopists in
providing care to patients. This guideline is not a rule
and should not be construed as establishing a legal standard of care or as encouraging, advocating, requiring,
or discouraging any particular treatment. Clinical decisions in any particular case involve a complex analysis
of the patients condition and available courses of action.
Therefore, clinical considerations may lead an endoscop-

Copyright 2016 by the American Society for Gastrointestinal Endoscopy

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ist to take a course of action that varies from these

guidelines.
Antithrombotic therapy is used to reduce the risk of
thromboembolic events in patients with conditions such as
atrial brillation (AF), acute coronary syndrome (ACS),
deep vein thrombosis (DVT), hypercoagulable states, and
endoprostheses. Antithrombotics include medications classied as anticoagulants or antiplatelet agents (APAs). Anticoagulants prevent the clotting of blood by interfering with the
native clotting cascade and include the following 4 drug
classes: vitamin K antagonists (eg, warfarin), heparin derivatives (eg, unfractionated [UFH] and low molecular weight
[LMWH], fondaparinux [Arixtra, GlaxoSmithKline, Research
Triangle Park, NC, USA]), direct factor Xa inhibitors (eg, rivaroxaban [Xarelto, Janssen Pharmaceuticals, Inc, Raritan,
NJ, USA], apixaban [Eliquis, Bristol-Myers Squibb Company,
Princeton, NJ, USA], edoxaban [Savaysa, Daiichi Sankyo
Co, LTD, Tokyo, Japan]), and direct thrombin inhibitors
(eg, dabigatran [Pradaxa, Boehringer Ingelheim Pharmaceuticals Inc, Ridgeeld, Conn, USA], hirudins, argatraban
[Acova, Abbott Laboratories, North Chicago, Ill, USA]).
APAs decrease platelet aggregation, thus preventing
thrombus formation. APAs include the thienopyridines (eg,
clopidogrel, [Plavix, Bristol-Myers Squibb/Sano Pharmaceuticals Partnership, Bridgewater, NJ, USA], prasugrel [Efent,
Eli Lilly and Company, Indianapolis, Ind, USA], ticlopidine
[Ticlid, Roche Pharmaceuticals, Nutley, NJ, USA], and ticagrelor [Brilinta, AstraZeneca, Wilmington, Del, USA]), the
protease-activated receptor-1 (PAR-1) inhibitor vorapaxar
(Zontivity, Merck Sharp & Dohme Corp, Whitehouse Station,
NJ, USA), glycoprotein IIb/IIIa receptor inhibitors (GPIIb/IIIa
inhibitors) (eg, abciximab [ReoPro, Eli Lilly and Company, Indianapolis, Ind, USA], eptibatide [Integrilin, Merck Sharp &
Dohme Corp, Whitehouse Station, NJ, USA], and tiroban
[Aggrastat, Medicure Pharma, Inc, Somerset, NJ, USA]),
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Management of antithrombotic agents for patients undergoing GI endoscopy

TABLE 1. System for rating the quality of evidence for guidelines

Quality of evidence
High quality
Moderate quality
Low quality

Definition

Symbol

Further research is very unlikely to change our confidence in the estimate of effect.

4444

Further research is likely to have an important impact on our confidence in the estimate of
effect and may change the estimate.

444O

Further research is very likely to have an important impact on our confidence in the estimate of
effect and is likely to change the estimate.

44OO

Any estimate of effect is very uncertain.

4OOO

Very low quality

Adapted from Guyatt et al.1

TABLE 2. Antithrombotic drugs: duration of action and approach to reversal when indicated
Approach to reversal based on procedural urgency
Drug class
APAs

Anticoagulants

Specific agent(s)

Duration of action

Elective

Urgent

Aspirin

7-10 days

NA

Hold, can give platelets

NSAIDs

Varies

NA

Hold

Dipyridamole (Persantine)

2-3 days

Hold

Hold

Cilostazol (Pletal, Otsuka Pharmaceutical

Co., Ltd., Tokushima, Japan)

2 days

Hold

Hold

Thienopyridines: clopidrogrel (Plavix)

prasugrel (Effient) ticlodipine (Ticlid)
ticagrelor (Brilinta)

5-7 days: clopidogrel, 3-5

days: ticagrelor
5-7 days: prasugrel
10-14 days98: ticlopidine

Hold

Hold

GPIIb/IIIa inhibitors: tirofiban (Aggrastat)

abciximab (ReoPro)
eptifibatide (Integrilin)

tirofiban: 1-2 seconds

abciximab: 24 hours
eptifibitide: 4 hours

NA

Hold
HD: tirofiban

PAR-1 inhibitor: vorapaxar (Zontivity)

5-13 days

Hold

Hold

Warfarin (Coumadin)

5 days

Hold

Vitamin K, PCC

UFH

IV 2-6 hours
SQ 12-24 hours

Hold

Protamine sulfate* (partial)

LMWH:
enoxaparin (Lovenox)
dalteparin (Fragmin, Pfizer Inc,
New York, NY, USA)

24 hours

Hold

Protamine sulfate, consider rVIIa

Fondaparinux (Arixtra)

36-48 hours

Direct factor Xa Inhibitor: rivaroxaban

(Xarelto) apixaban (Eliquis)
edoxaban (Savaysa)

See Tables 7 and 8

Hold

Charcoal (if last intake within 2-3 hours);

nonactivated PCC or activated PCC

Direct thrombin inhibitor, oral: dabigatran

(Pradaxa)
IV: Desirudin (Iprivask, Aventis
Pharmaceuticals Inc.,
Bridgewater, NJ, USA)

See Table 9

Hold

Charcoal (if last intake within 2-3 hours);

nonactivated PCC or activated PCC; HD

Protamine sulfate, consider rVIIa

NSAIDs, Nonsteroidal anti-inflammatory drugs; NA, not applicable; HD, hemodialysis; PCC, prothrombin complex concentrate; rVIIa, recombinant factor VIIa.
*Caution: Can cause severe hypotension and anaphylaxis.

aspirin (acetylsalicylic acid [ASA]), and nonsteroidal antiinammatory drugs. The duration of action and reversal
routes for the antithrombotic drug classes are described in
Table 2.
Adverse events of antithrombotic therapy include GI
bleeding,2,3 and their use increases the risk of hemorrhage
after some endoscopic interventions.4-6 For patients taking
these medications who require endoscopy, one should
consider the following important factors: (1) the urgency
4 GASTROINTESTINAL ENDOSCOPY Volume 83, No. 1 : 2016

of the procedure, (2) the bleeding risk of the procedure,

(3) the effect of the antithrombotic drug(s) on the bleeding
risk, and (4) the risk of a thromboembolic event related
to periprocedural interruption of antithrombotic agents.7

PROCEDURE RISKS
Common endoscopic procedures vary in their potential
to induce bleeding, and these have been outlined in other
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Management of antithrombotic agents for patients undergoing GI endoscopy

TABLE 3. Procedure risk for bleeding (overall)

Higher-risk procedures
Polypectomy
Biliary or pancreatic sphincterotomy

Low-risk procedures
Diagnostic (EGD, colonoscopy, flexible sigmoidoscopy) including mucosal biopsy
ERCP with stent (biliary or pancreatic) placement or papillary balloon dilation without sphincterotomy

Treatment of varices
PEG placement*

Push enteroscopy and diagnostic balloon-assisted enteroscopy

Therapeutic balloon-assisted enteroscopy

EUS with FNAy

Capsule endoscopy
Enteral stent deployment (Controversial)

Endoscopic hemostasis

EUS without FNA

Tumor ablation

Argon plasma coagulation

Cystgastrostomy

Barretts ablation

Ampullary resection
EMR
Endoscopic submucosal dissection
Pneumatic or bougie dilation
PEJ
PEJ, Percutaneous endoscopic jejunostomy.
*PEG on aspirin or clopidogrel therapy is low risk. Does not apply to DAPT.
yEUS-FNA of solid masses on ASA/NSAIDs is low risk.

ASGE guidelines (Table 3).8 Studies on postprocedural

bleeding risks have been conducted in patients who are not
on complex antithrombotic regimens and thus may not
accurately reect the bleeding risk of patients using newer
antithrombotic therapies. Traditionally, low-risk procedures
have included diagnostic EGD, colonoscopy, ERCP without
sphincterotomy, biliary stent placement, and push or
balloon-assisted enteroscopy. Mucosal biopsy sampling performed as part of these procedures confers a low risk of GI
bleeding. Similarly, EUS without FNA, capsule endoscopy,
and argon plasma coagulation8 are low risk. Nonachalasia
esophageal dilation has been associated with a low risk of
bleeding in large series9,10,11; however, the safety of dilation
while on anticoagulants is unknown, and the potential for
an inaccessible site of bleeding argues for caution in this
setting. High-risk endoscopic procedures are associated with
a potential for bleeding that requires an intervention, such as
hospitalization, transfusion, endoscopic treatment, or surgery.12 These high-risk procedures include polypectomy,13,14
therapeutic balloon-assisted enteroscopy (other than argon
plasma coagulation),15,16 endoscopic sphincterotomy,17 EUS
with FNA, percutaneous endoscopic gastrostomy,18-20 percutaneous endoscopic jejunostomy,21 tumor ablation
(esophagus, stomach, colon, and rectum),22 endoscopic
submucosal dissection,23 EMR,24 pneumatic balloon dilation
for achalasia,25 treatment of varices,26 ampullary resection,
per-oral endoscopic myotomy,27 cystoenterostomy,28 and
endoscopic therapy of Zenkers diverticulum.29 The risk of
bleeding after polypectomy ranges from .3% to 10% and
depends on a number of factors, including the polyp size,
location, morphology (nonpolypoid, sessile, pedunculated),
resection technique (cold or hot forceps, cold snare, or
snare cautery), and type of cautery used.
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TABLE 4. CHA2DS2-VASc scoring system

CHA2DS2-VASc score or
assessment

Risk of stroke
(CVA)

% Risk of annual
CVA

Low

Moderate

1.3

High

2.2

High

3.2

High

4.0

High

6.7

High

9.8

High

9.6

High

6.7

High

15.2

CHA2DS2-VASc, Congestive heart failure [1 point], Hypertension [1 point], Age  75

years [2 points], Diabetes mellitus [1 point], Stroke [2 points], Vascular disease [1
point], Age 65-74 years [1 point], Sex category, ie, female sex [1 point].
CVA, cerebrovascular accident.

There is controversy with regard to whether enteral

stent placement is high or low risk. One retrospective review of 85 patients with esophageal stents described a
bleeding risk as high as 5.3%.30 However, subsequent
prospective multicenter studies as well as systematic
reviews have described bleeding rates in the range of
.5% to 1% in a variety of GI locations.31,32

CONDITION RISKS
The probability of a thromboembolic event related to the
temporary interruption of antithrombotic therapy for an
endoscopic procedure depends on the indication for
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Management of antithrombotic agents for patients undergoing GI endoscopy

TABLE 5. Risk for thromboembolic event in patients with mechanical heart valve(s) or VTE on anticoagulation37
Clinical indication for warfarin therapy
Annual
risk

Mechanical heart valve

VTE

High

 Any mitral valve prosthesis

 Any caged-ball or tilting disc aortic valve prosthesis
 Recent (within 6 months) CVA or TIA

 Recent (within 3 months) VTE

 Severe thrombophilia (deciency of protein C, protein S, or
antithrombin; antiphospholipid antibodies; multiple
abnormalities)

Medium

 Bileaet aortic valve prosthesis and one or more of the following risk
factors: AF, prior CVA or TIA, hypertension, diabetes, congestive heart
failure, age  75 years

 VTE within the past 3-12 months

 Nonsevere thrombophilia (heterozygous factor V Leiden or
prothrombin gene mutation)
 Recurrent VTE
 Active cancer (treated within 6 months or palliative)

Low

 Bileaet aortic valve prosthesis without AF and no other risk factors

for CVA

 VTE > 12 months previous and no other risk factors

VTE, venous thromboembolism; CVA, cerebrovascular accident; TIA, Transient ischemic attack; AF, atrial fibrillation.

antithrombotic therapy and individual patient characteristics.

For example, in patients with nonvalvular AF, important determinants of risk for a cerebrovascular accident (CVA) are
included in the CHA2DS2-VASc index (Table 4).33 This score
ranges from 0 to 9 and considers thromboembolic risk
factors of congestive heart failure (1 point), hypertension
(1 point), age  75 years (2 points), diabetes (1 point),
stroke (2 points), vascular disease (prior myocardial
infarction [MI], peripheral artery disease, or aortic plaque)
(1 point), age 65 to 74 years (1 point), and sex category
(female) (1 point). The higher the score, the greater the
thromboembolic risk, and patients with a score of 2 are
considered to be at high risk of thromboembolism
(>2.2%/year). These patients are frequently prescribed an
anticoagulant to mitigate thromboembolic risk.
High thrombosis risk scenarios for patients on APA therapy include placement of drug-eluting coronary stents 
12 months previously or bare metal coronary stents  1
month previously. For patients with ACS, a bare metal coronary stent placed 12 months previously is considered a
high-risk setting.4 Endoscopists should be aware of
specic clinical risk factors that will predispose a patient to
higher rates of stent occlusion beyond 1 year after stent
insertion and approach modication of antiplatelet
regimens cautiously in these cases. These patients include
those with a prior history of stent occlusion, because 1 in 5
patients who experience a rst thrombosis will experience
a second stent occlusion at a rate of .6% per year over the
rst 3 years,34,35 with a cumulative risk of cardiac death of
27.9%. Patients with ACS or ST elevation MI, multivessel
percutaneous coronary intervention, diabetes, renal failure,
or diffuse coronary artery disease are also at higher risk of
stent occlusion or ACS events with alteration of antithrombotic therapy.36
Patients with previous venous thromboembolism (VTE)
on anticoagulation or 1 or more mechanical heart valves
have different risk factors for thromboembolic events
(Table 5). Specic clinical variables divide patients into
6 GASTROINTESTINAL ENDOSCOPY Volume 83, No. 1 : 2016

low-, medium-, and high-risk groups. Among patients with

VTE, time from initial VTE, history of recurrent VTE with antithrombotic interruption, and presence of underlying
thrombophilia are most predictive of future thromboembolic risk. For patients with mechanical heart valves the
type, number, and location of valvular prostheses and the
presence or absence of associated heart failure and AF determine the annual risk of thromboembolic events. Bioprosthetic valves are considered low risk.37

ANTIPLATELET AGENTS
ASA is a cyclooxygenase inhibitor that is used alone or in
combination with other APAs. It is used to inhibit platelet
aggregation for prophylaxis of secondary cardioembolic
phenomena after occurrence of a stroke or MI. In patients
with a >10% 10-year risk of heart attack or stroke,38
primary cardioprophylaxis with low-dose ASA therapy is
recommended. ASA causes irreversible inhibition of the cyclooxygenase 1 and 2 enzyme systems. After cessation of
ASA, 7 to 9 days are required to regain full platelet
function.39
Dipyridamole (Persantine, Teva Pharmaceuticals USA,
Sellersville, Pa, USA) reversibly inhibits platelet aggregation. This drug is used in combination with ASA in the secondary prevention of stroke and off-label for primary
stroke prevention. The mechanism of action of this drug
is controversial40; both inhibition of cyclic nucleotide
phosphodiesterase and blockade of the uptake of
adenosine have been suggested. Dipyridamole has an
elimination half-life of 12 hours and duration of action of
about 2 days after discontinuation.
The most common APAs used after ASA therapy are the
thienopyridine agents. These drugs bind to the P2Y12
component of the ADP receptors, which prevents activation of the GPIIb/IIIa receptor complex, thereby reducing
platelet aggregation. The class includes ticlopidine (Ticlid),
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Management of antithrombotic agents for patients undergoing GI endoscopy

clopidogrel (Plavix), prasugrel (Efent), and ticagrelor

(Brilinta). Ticlopidine (Ticlid), the rst widely available
thienopyridine agent, has largely been supplanted in clinical use by newer second-generation agents because of
concerns regarding hematologic side effects (such as neutropenia, thrombotic thrombocytopenia purpura, and hemolytic uremic syndrome). Clopidogrel (Plavix) is
approved for secondary prevention of MI or stroke and
in the primary management of established peripheral
vascular disease. Clopidogrel (Plavix) efcacy can be
limited by variations of the ABCB13435 TT and CYP2C19
genotypes of cytochrome P450 enzymes, which alter hepatic metabolism of the clopidogrel prodrug to its active
thiol metabolite.41,42 This altered metabolism results in variable antiplatelet effects and adverse cardiac events,43
including stent thrombosis44 and postpercutaneous
coronary intervention ischemic events.45 The minimum
duration of discontinuation of clopidogrel that allows for
restoration of normal platelet aggregation is 5 to 7 days.37
Third-generation thienopyridine agents include prasugrel (Efent) and ticagrelor (Brilinta). Similar to clopidogrel (Plavix), prasugrel (Efent) is a prodrug that requires
conversion by the cytochrome P450 hepatic enzymes;
however, unlike clopidogrels (Plavix) multistep conversion
process to an active metabolite, the activation of prasugrel
(Efent) occurs in a single hepatic step. The pharmacologic characteristics of prasugrel (Efent) overcome some
of the limitations of clopidogrel (Plavix) but at the risk of
increased bleeding. Because of this, the U.S. Food and
Drug Administration (FDA) approved the drug with a black
box warning specically noting that prasugrel (Efent)
should not be used in patients with active bleeding, a history of transient ischemic attack or CVA, or likely to undergo urgent coronary bypass graft surgery. Similar to
clopidogrel (Plavix), the mechanism of action is the irreversible inhibition of the P2Y12 receptor; thus, the minimum duration of discontinuation of prasugrel that allows
for restoration of normal platelet aggregation is 5 to 7
days. Unlike clopidogrel (Plavix), prasugrel (Efent)
achieves a much higher level of platelet inhibition and is
unaffected by variants of the CYP2C19 or ABCB1 genotypes.46-48
Ticagrelor (Brilinta) is the rst reversible oral P2Y12
antagonist and an alternative therapy for ACS. This
drug is quickly absorbed, does not require metabolic
activation, and has a rapid antiplatelet effect that closely
parallels drug-exposure levels. Unlike clopidogrel (Plavix) and prasugrel (Efent), the reversible inhibition of
the P2Y12 receptor permits a shorter interval of discontinuation, 3 to 5 days, to recover adequate platelet
function.49
In January 2014 the FDA approved a rst-in-class antiplatelet medication, vorapaxar (Zontivity). This agent is a
competitive and selective inhibitor of PAR-1, the major
thrombin receptor on human platelets. It has been shown
in clinical trials to reduce the risk of MI, stroke, CV death,
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and need for revascularization procedures in patients with

a previous MI or peripheral artery disease when prescribed
in conjunction with traditional dual antiplatelet therapy
(DAPT).50 However, this intensication of antiplatelet
effect, via a novel pathway, is associated with an
increased risk of moderate or severe bleeding in 4.2%
versus 2.5% (placebo) and a 66% increased risk of
bleeding overall. Currently, this agent is associated with a
black box warning identifying a high risk of bleeding and
contraindication in patients with a history of stroke,
transient ischemic attack, or intracranial hemorrhage.
Vorapaxar displays signicant inhibition of platelet
aggregation that remains up to 4 weeks after
discontinuation.51 The actual impact of this drug on the
GI tract is relatively unknown, and postmarketing data
are needed to identify these risks.

ANTICOAGULANT AGENTS
Warfarin
Warfarin (Coumadin, Bristol-Myers Squibb Company,
Princeton, NJ, USA) is an oral anticoagulant that inhibits
the vitamin Kdependent clotting factors II, VII, IX, and
X and proteins C and S. Its activity is measured via the International Normalized Ratio (INR). The INR decreases
to 1.5 in approximately 93% of patients within 5 days of
discontinuing therapy.52

Novel oral anticoagulants

The novel oral anticoagulants (NOACs) include the
direct thrombin inhibitor dabigatran and the direct factor
Xa inhibitors (eg, rivaroxaban [Xarelto], apixaban [Eliquis],
edoxaban [Savaysa]) (Table 2). Dabigatran (Pradaxa) was
the rst NOAC approved in the United States for
prevention of CVA and systemic embolism in patients
with nonvalvular AF. It is metabolized and excreted
primarily by the kidneys, reaching maximum effect 1.25
to 3 hours after ingestion, with a half-life of 12 to 14 hours.
Assessment of the degree of anticoagulation is best
achieved by assessment of the Ecarin Clotting Time or
the dilute thrombin time, neither of which is readily available in the acute clinical setting. Partial thromboplastin
time and prothrombin time vary in their sensitivities to dabigatran depending on the reagents used and can be
normal in spite of circulating therapeutic levels of dabigatran. However, a normal activated partial thromboplastin
time effectively rules out a clinically signicant circulating
drug level. Timing of discontinuation before an endoscopic
procedure is dictated by the patients creatinine clearance
because 80% of excretion occurs via the kidneys
(Table 6).53
Rivaroxaban (Xarelto) is approved in the United States
for prevention of VTE after orthopedic surgery, treatment of VTE, and prevention of CVA and systemic embolism in patients with AF. Apixaban (Eliquis) is FDA
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Management of antithrombotic agents for patients undergoing GI endoscopy

TABLE 6. Periprocedural management of dabigatran (Pradaxa)53

Timing of discontinuation before procedure
Creatinine
clearance (mL/min)

Time to onset
of action (h)

Half-life (h)

Moderate procedural
bleeding risk (2-3 half-lives)

High procedural bleeding

risk (4-5 half-lives)

>80
50-80

1.25-3

13 (11-22)

1-1.5 days

2-3 days

1.25-3

15 (12-34)

1-2 days

2-3 days

30-49

1.25-3

18 (13-23)

1.5-2 days

3-4 days

29

1.25-3

27 (22-35)

2-3 days

4-6 days

approved for prevention of systemic embolism in AF patients, postorthopedic surgery prevention of VTE, and
for treatment and reduction of recurrence of VTE. Edoxaban (Savaysa) is FDA approved for AF and VTE treatment indications. The effect of the anti-Xa
anticoagulants is best assessed by measuring anti-Xa
levels with drug-specic calibrators. Prothrombin time
and activated partial thromboplastin time are crude measures of drug effect and are insensitive tests, often only
minimally prolonged or even normal in spite of therapeutic drug levels. However, normal test results rule
out high circulating drug levels. There is no reliable
serum assay to assess the degree of anticoagulant activity with these agents at this time. Caution should be
used in interpretation of the activated partial thromboplastin time in situations of drug toxicity because the
assay is subject to a ceiling effect and does not reliably
capture the severity of the anticoagulant effect.53
In the periendoscopic period there are 3 important pharmacodynamic considerations when holding and restarting
an anticoagulant: (1) time to maximum effect, (2) half-life,
and (3) excretion of the drug. Rivaroxaban (Xarelto), apixaban (Eliquis), and edoxaban (Savaysa) all have a relatively
short time to maximal effect (eg, 2-4 hours with rivaroxaban
[Xarelto], 1-3 hours with apixaban [Eliquis]), a half-life
ranging from 8 to 15 hours, and variable excretion by the kidneys (rivaroxaban [Xarelto] 66% and apixaban [Eliquis]
25%). To minimize the risk of bleeding, these medications
should be stopped for at least 2 half-lives before high-risk
procedures, and their dosing should be adjusted in the
setting of renal impairment (Tables 7-9).54
An antidote for dabigatran (Pradaxa) has been approved
following accelerated review by the FDA.55 This antidote is
idarucizumab (Praxbind, Boehringer Ingelheim, Inc,
Ridgeeld, CT, USA) and is approved for use in cases of lifethreatening, uncontrolled bleeding or prior to emergency
surgery. Another reversal agent that is currently under
evaluation is Aripazine (PER977, Perosphere, Inc, Danbury,
CT, USA), which binds to UFH and LMWH; factor Xa
inhibitors; edoxaban (Savaysa); rivaroxaban (Xarelto) and
apixaban (Eliquis); and dabigatran (Pradaxa).56 Animal
studies and pharmacodynamics studies with Aripazine have
demonstrated reversal of edoxaban (Savaysa) to 10% of
baseline values within 10 minutes of drug delivery. Finally,
8 GASTROINTESTINAL ENDOSCOPY Volume 83, No. 1 : 2016

TABLE 7. Periprocedural management of apixaban (Eliquis)54

Creatinine
clearance
(mL/min)

Time to onset of
action (h)

Timing of discontinuation before

high-risk endoscopic procedure
(day)

>60

1-3

1 or 2

30-59

1-3

15-29

1-3

TABLE 8. Periprocedural management of rivaroxaban (Xarelto)54

Time to onset
of action (h)

Timing of discontinuation
before high-risk
endoscopic
procedure (day)

>90

2-4

1

60-90

2-4

30-59

2-4

15-29

2-4

Creatinine
clearance
(mL/min)

Andexanet alfa has been studied in a phase II trial and

shows promise as yet another reversal agent, by decreasing
anti-Xa activity and reducing plasma concentrations of free
apixaban (Eliquis) in healthy volunteers.57 Future studies
are needed to demonstrate efcacy in humans and in the
setting of major hemorrhage.

Parenteral and subcutaneously administered

anticoagulants
UFH administered intravenously has a half-life of 60 to
90 minutes, and anticoagulant effects dissipate 3 to 4 hours
after discontinuation. LMWH (enoxaparin [Lovenox, SanoAventis U.S., LLC, Bridgewater, NJ, USA] and dalteparin
[Fragmin, Pzer Inc, New York, NY, USA]) is administered
subcutaneously at therapeutic doses for bridging and for
the treatment of VTE. It is also prescribed at reduced doses
for the prevention of VTE in low-risk patients. The last dose
of these agents should be given 24 hours before the anticipated procedure at 50% of the total daily dose.37
Fondaparinux (Arixtra) is a synthetic and specic inhibitor of factor Xa. It is approved in the United States for
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Management of antithrombotic agents for patients undergoing GI endoscopy

TABLE 9. Periprocedural management of edoxaban (Savaysa)99

Creatinine
Time to
clearance
onset
(mL/min) of action (h)

Half-life
(h)

Timing of discontinuation
before high-risk procedure
(h)

>60

1-2

8.6

At least 24

30-60

1-2

9.4

At least 24

15-30

1-2

16.9

At least 24

15

1-2

No data

No data

perioperative DVT prophylaxis and for the initial treatment

of acute DVT/pulmonary embolism. It is administered subcutaneously and is distinct from LMWH. Fondaparinux
(Arixtra) has a high afnity for antithrombin III, which potentiates inhibition of factor Xa. The minimum recommended time for discontinuation of this drug before a high-risk
procedure is 36 hours.58
Desirudin (Iprivask, Aventis Pharmaceuticals Inc.,
Bridgewater, NJ, USA) is a direct thrombin inhibitor
approved for DVT prophylaxis after hip replacement and
is administered subcutaneously. Recommendations are to
discontinue this medication 10 hours before a high-risk
procedure.59

COMMON ELECTIVE ENDOSCOPIC PROCEDURES

IN PATIENTS ON ANTITHROMBOTIC THERAPY
Because of the paucity of high-quality evidence
regarding bleeding risks associated with antithrombotic
therapies prescribed in dual (ASA thienopyridine;
ASA anticoagulant) and triple combinations (ASA
thienopyridine anticoagulant), a one-size-ts-all
approach to recommendations regarding the periprocedural management of antithrombotic agents undergoing
endoscopy is not possible at this time. A summary of the
available evidence is presented below (Table 10), with
the awareness that additional research is required and
will likely inuence future recommendations regarding
periendoscopic management of third-generation thienopyridines, PAR-1 inhibitors, and NOAC prescribed in combination with ASA.60
With regard to polypectomy, there are modest data to
support the use of cold snare rather than conventional
polypectomy in those patients anticoagulated with
warfarin (Coumadin). In a small study of warfarin (Coumadin), 70 patients with 159 polyps up to 10 mm were
randomized to cold polypectomy versus conventional
snare. Delayed bleeding requiring hemostasis occurred
less commonly after cold snare polypectomy than conventional polypectomy despite continuation of anticoagulants
(0% vs 14%, P Z .027).61 Further data in the area of
optimal endoscopic technique for patients prescribed
antithrombotic agents are necessary to better inform
endoscopic decisions and clinical best practice.
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RISK OF STOPPING ANTITHROMBOTIC

THERAPY BEFORE ELECTIVE ENDOSCOPY
When antithrombotic therapy is required for a short
period of time (ie, after VTE or bare metal stent insertion),
elective procedures should be delayed until such therapy is
no longer indicated. In patients who need antithrombotic
therapy for a longer period of time (ie, after drug-eluting
stent placement or post-ACS), careful consideration of
the cardioembolic risk must be made before temporary
drug cessation to avoid spontaneous stent occlusion,
ACS, and death.62-64 Decisions about discontinuing or temporary cessation of these agents should be individualized
and discussed, before the endoscopic procedure, with
the patient and, optimally, the prescribing provider (cardiologist, neurologist, hematologist, primary care physician).
It is important to recognize that in some high-risk patients,
antithrombotic agents may not be able to be stopped.

Cessation of anticoagulant
Current guidelines from the American College of Chest
Physicians (ACCP) regarding the management of anticoagulation in patients with AF and/or valvular heart disease
undergoing elective invasive procedures are summarized
in Table 6.42 The absolute risk of an embolic event in
patients whose anticoagulation is interrupted for 4 to 7
days is approximately 1%.65,66 After temporary discontinuation of warfarin (Coumadin), reinitiation of drug should
occur within 4 to 7 days of initial drug discontinuation to
ensure no increased risk of thromboembolic event and
can occur on the same day in many patients.67

Role of bridge therapy

To reduce the risk of thromboembolic events, patients
on warfarin (Coumadin) may be switched to a shorteracting (ie, bridge [Table 11]) anticoagulant in the
periendoscopic period. Evidence for the use of UFH and
LMWH (enoxaparin) as bridge therapies for endoscopic
procedures in patients on warfarin (Coumadin) is limited.
One study of 98 patients undergoing endoscopy (EGD
and/or colonoscopy) with bridge therapy using
bemiparin, an ultra-LMWH, found no thromboembolic
events and only 2 major bleeding episodes that were unrelated to endoscopy.68 Current guidelines (2011 American
College of Cardiology Foundation/American Heart
Association [AHA]/Heart Rhythm Society guideline on AF
and the 2014 AHA/American College of Cardiology [ACC]
guideline on valvular heart disease) regarding the
management of anticoagulation in patients with AF and/
or valvular heart disease undergoing elective invasive
procedures are summarized in Table 10.69,70 A meta-analysis71 showed that vitamin K antagonisttreated patients
receiving periprocedural bridging therapy with heparin
appear to be at increased risk of both overall and major
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Management of antithrombotic agents for patients undergoing GI endoscopy

TABLE 10. Summary for available evidence for bleeding risk with common endoscopic procedures on antithrombotic agents
Therapeutic warfarin/heparin
Diagnostic EGD/colonoscopy /- biopsy
Colonoscopic polypectomy
Sphincterotomy
EUS/FNA

Low risk

100

High risk

ASA/NSAID

112

Low104

113

Low75,98,115

Low

75,101-109

High

High110

Unknown

Low17

111

Unknown

Low111

Low for clopidogrel only114

Low114

High

PEG (does not apply to DAPT)

Thienopyridine

Unknown

ASA, acetylsalicylic acid, or aspirin; NSAID, nonsteroidal anti-inflammatory drug; DAPT, dual antiplatelet therapy.

TABLE 11. Approach to bridge therapy for warfarin (Coumadin)69-70

Condition
AF

Valvular heart
disease

Associated diagnosis

Management

None
CHA2DS2-VASc score < 2

No bridge
recommended

Mechanical valves
History of CVA
CHA2DS2-VASc score  2

Bridge therapy
recommended

Bileaflet mechanical AVR

No bridge
recommended

Mechanical AVR and any

thromboembolic risk factor
Older-generation mechanical AVR
Mechanical mitral valve
replacement

Bridge therapy
recommended

AF, atrial fibrillation; CHA2DS2-VASc, Congestive heart failure, Hypertension, Age > 75
years [2 points], Diabetes Mellitus, Stroke [2 points], Vascular disease, Age 65-74
years, Sex category [ie, female sex]; CVA, cerebrovascular accident; AVR, aortic valve
replacement.

bleeding and at similar risk of thromboembolic events

compared with nonbridged patients.
A recently published randomized controlled trial72
sought to better dene the role of periprocedural heparin
bridging in 1884 patients with nonvalvular AF undergoing
an elective invasive procedure. Patients were randomized
to bridging versus no-bridging, and results demonstrated
the heparin-bridged group experienced more major
bleeding (3.2% vs 1.3%) than the nonbridged group, with
no difference in arterial thromboembolism (.3% vs .4%).
Of note, these data should not be applied to those patients
with higher risk for thromboembolism, such as patients
with valvular AF, mechanical valves, left ventricular assist devices, recently diagnosed thromboembolism, AF with
congestive heart failure, or in the post-ACS setting.72

Cessation of APA (including DAPT)

The most common antithrombotic strategy prescribed
in the United States with regard to patients on DAPT is
to hold the thienopyridine in the periendoscopic period
and continue the aspirin. Eisenberg et al73 performed a
systematic review of 161 reported cases of late stent
thrombosis (>30 days but <1 year after stent placement)
and very late stent thrombosis (>1 year after stent
placement). Patients who discontinued both ASA and a
thienopyridine had a median time to event of 7 days. In
10 GASTROINTESTINAL ENDOSCOPY Volume 83, No. 1 : 2016

those who discontinued thienopyridine but remained on

ASA, the median time to an event was 122 days. There
were a total of 6 cases (6%) of stent thrombosis within
10 days of thienopyridine cessation, suggesting shortterm discontinuation between 30 days and 1 year from
drug-eluting coronary stent placement (late stent thrombosis) might be relatively safe but still carry some risk.
Best practice recommendations for the management of
DAPT (ie, ASA thienopyridine APA) are summarized in
the American College of Cardiology Foundation and American College of Gastroenterology consensus statement
(Table 12).36

REINITIATION OF ANTITHROMBOTIC AGENTS

AFTER ELECTIVE ENDOSCOPY
There is consensus that antithrombotic therapy should
be resumed upon completion of the procedure.36,74
The benets of immediate reinitiation of antithrombotic
therapy for the prevention of thromboembolic events
should be weighed against the risk of hemorrhage associated with the specic agent, the time to onset of the medication, and on procedure-specic circumstances (eg, risk
of bleeding after sphincterotomy, polypectomy, or EMR).
Most existing literature on this topic addresses reinitiation
of warfarin or heparin and heparin-like products. Less is
known regarding timing to reinitiation of APAs and NOACs.
In 1 study involving 94 patients who had undergone 109
colonoscopies (including hot biopsy or snare polypectomy
in 47%), patients were instructed to restart warfarin (Coumadin) therapy on the day after endoscopy.75 Only 1 case
(0.9%) of procedure-related bleeding occurred after 7 days
of warfarin (Coumadin) therapy and required hospitalization and transfusion. None of the patients undergoing diagnostic colonoscopy experienced bleeding. Conversely, a
second study involving 173 patients found that resuming
warfarin (Coumadin) or heparin within 1 week after polypectomy was associated with an increased risk of bleeding
(OR 5.2; 95% CI, 2.2-12.5).76 Because of the ongoing risk of
thromboembolic events, the 2014 AHA/ACC guideline (on
the management of valvular heart disease) recommends
that warfarin (Coumadin) be restarted within 24 hours of
the procedure in patients with valvular heart disease and
a low-risk for thromboembolism. In patients at high risk
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Management of antithrombotic agents for patients undergoing GI endoscopy

TABLE 12. Best practice recommendations for the management of

DAPT36
Avoid cessation of all antiplatelet therapies after PCI with stent
placement.
Avoid cessation of clopidogrel (even when aspirin is continued) within
the first 30 days after PCI and either DES or BMS placement when
possible.
Defer elective endoscopic procedures, possibly up to 12 months, if
clinically acceptable from the time of PCI to DES placement.
Perform endoscopic procedures, particularly those associated with
bleeding risk, 5-7 days after thienopyridine drug cessation. ASA
should be continued.
Resume thienopyridine and ASA drug therapy after the procedure
once hemostasis is achieved. A loading dose of the former should be
considered among patients at risk for thrombosis.
Continue platelet-directed therapy in patients undergoing elective
endoscopy procedures associated with a low-risk for bleeding.
DAPT, dual antiplatelet therapy; BMS, Bare metal stent(s); DES, drug-eluting stent(s);
PCI, percutaneous coronary intervention; ASA, acetylsalicylic acid, or aspirin.

for thromboembolism, UFH or LMWH should be restarted

as soon as bleeding stability allows and continued until
the INR reaches an appropriate therapeutic level.70 UFH
may be restarted 2 to 6 hours after a therapeutic
procedure. The optimal time to restart LMWH after
endoscopy has not been determined. The 2012 ACCP
guidelines recommend delaying reinitiation of LMWH 48
to 72 hours after surgery in patients believed to be at
high risk for bleeding adverse events.37
There are no data to inform optimal timing of resumption of NOACs after endoscopic procedures. Because these
agents have a short onset of action (Tables 7-10), if a NOAC
cannot be restarted within 24 hours after a high-risk procedure because of concern regarding the adequate hemostasis, then thromboprophylaxis (ie, UFH bridge)
should be considered for patients at high risk for
thromboembolism.53,54
Cardiac ASA should not be discontinued in most cases.
Other APAs should be resumed once hemostasis has been
achieved (Table 12).

ENDOSCOPIC PROCEDURES IN THE ACUTELY

BLEEDING PATIENT ON ANTITHROMBOTIC
THERAPY
Endoscopic evaluation and therapy in patients using antithrombotics with active GI bleeding is both warranted
and safe.7 The most common etiologies for upper GI
blood loss in these patients are peptic ulcer disease and
erosive diseases of the esophagus, stomach, and
duodenum.77 Diverticular bleeding is the most common
cause of lower GI bleeding.78,79

Anticoagulants
In 1 retrospective series of 52 patients, correction of the
INR to between 1.5 and 2.5 allowed successful endoscopic
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diagnosis and therapy at rates comparable with those

achieved in non-anticoagulated patients.80 In a large
series in which 95% of patients had an INR between 1.3
and 2.7, endoscopic therapy achieved initial success in
95% of patients (233/246) using a variety of hemostatic
techniques, including injection therapy, heater probe,
and hemoclips.81 Although the rebleeding rate in this
series was 23%, the INR level before endoscopy was not
a predictor of rebleeding. In another retrospective study,
rates of rebleeding in patients with supratherapeutic INRs
(4.0) were not signicantly different from those with
INRs in the therapeutic range (2.0-3.9).79 Finally, in a
systematic review of 1869 patients with nonvariceal
upper GI bleeding, INR at initial presentation was found
not to predict the risk of rebleeding.82 These data
suggest that endoscopic hemostatic therapy is very
effective even in patients with moderately elevated INR,
normalizing the INR does not reduce rebleeding but
does delay time to endoscopy, and INR at the time of
endoscopy may not be predictive of rebleeding. Pending
further data, performing endoscopic therapy in bleeding
patients with INRs < 2.5 is reasonable.
The decision to stop, reduce, and/or reverse antithrombotic therapy (and thereby risking thromboembolic consequences) must be weighed against the risk of continued
bleeding. The risk of thromboembolic events was shown
to be low in 2 small studies that withheld warfarin (Coumadin) for 4 to 15 days before endoscopy (1/27 patients and
0/28 patients, respectively).83,84 The ACCP recommends
that warfarin (Coumadin) be held and rapid reversal of anticoagulation with 4-factor prothrombin complex (PCC) be
used for patients with vitamin K antagonist-associated major bleeding rather than fresh frozen plasma. They also suggest the additional use of vitamin K be given (5-10 mg by
slow IV) rather than reversal with coagulation factors
alone.85 PCC contains the vitamin Kdependent factors
II, VII, IX, and X either in nonactivated form
(nonactivated PCCs) or partially activated form (activated
PCCs; individual drug: Feiba). Some of the nonactivated
PCCs contain relatively little factor VII, and these PCCs
are referred to as 3-factor PCCs (Bebulin, Baxter Healthcare
Corporation, Westlake Village, Calif, USA; Prolnine, Grifols Biologicals Inc, Los Angeles, Calif, USA). In 2012 the
FDA approved a 4-factor PCC (Kcentra, CSL Behring LLC,
Kankakee, Ill, USA) for vitamin K antagonist reversal in patients with acute major bleeding or need for an urgent surgery/invasive procedure. For warfarin (Coumadin) reversal,
the 4-factor PCC is the appropriate reversal agent. However, a combination of 3-factor PCC and low dose of recombinant factor VIIa can also be used when the 4-factor agent
is unavailable.86 The 2014 AHA/ACC guideline on the
management of valvular heart disease recommends that
fresh frozen plasma (which is not recommended in the
ACCP 2012 guideline on the management of
anticoagulant therapy, mentioned earlier in this
paragraph) or PCC is reasonable in patients with
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Management of antithrombotic agents for patients undergoing GI endoscopy

mechanical valves and uncontrollable bleeding who

require reversal of anticoagulation. High-dose vitamin K
should not be given routinely because this may create a hypercoagulable condition.70
In the event of massive hemorrhage, hemodialysis can
be used in patients receiving dabigatran (Pradaxa) but
not for rivaroxaban (Xarelto), edoxaban (Savaysa), and
apixaban (Eliquis) because of their decreased renal excretion and because they are highly protein bound. Although
factor VIIa and 4-factor PCC have been used in these situations, their value in reversing the clinical anticoagulant effects, and controlling clinical hemorrhage is uncertain.87

Antiplatelet agents
For patients on APAs with life-threatening or serious
bleeding, options include stopping these agents and/or
administration of platelets. Most patients will require
resumption of antithrombotic therapy after endoscopic control of GI bleeding. There are very limited data to guide the
timing of reinitiation of antiplatelet therapy; however, current multidisciplinary cardiac and GI society consensus
statements recommend reinitiation of antiplatelet therapy
as soon as hemostasis is achieved.36,74 For patients who
develop ASA-related peptic ulcer disease bleeding, resumption of ASA with concurrent proton pump inhibitor therapy
is superior to switching to clopidogrel alone for the prevention of recurrent GI bleeding.88,89 The importance of prompt
resumption of cardiac aspirin is critical as demonstrated by a
randomized control trial by Sung et al90 that showed no
increased risk of postprocedural bleeding associated with
continued ASA use but a clear increase in 30-day mortality
in cardiac patients in whom ASA was not resumed.

ENDOSCOPY IN THE PATIENT WITH

INTRACORONARY STENTS OR ACS TAKING
ANTITHROMBOTIC DRUGS
Elective endoscopy in the patient with an
intracoronary stent
Use of DAPT may confer a 3-fold increase in the risk of
upper GI bleeding over single-agent antithrombotic therapy.2,3,91 Given the current evidence, all elective high-risk
endoscopic procedures in patients on DAPT should be delayed until the patient has received the minimum length of
therapy as recommended by American College of Cardiology Foundation/ACG guidelines.36 Once this period has
elapsed, the decision to proceed with such procedures
should be made after discussion of the associated risks
and benets with the patient and relevant medical
professionals.

Urgent endoscopy in the patient with ACS or

recently placed vascular stent
Antithrombotic agents are commonly used in the management of ACS in patients with recently placed intracoro12 GASTROINTESTINAL ENDOSCOPY Volume 83, No. 1 : 2016

nary stents. Many of these patients receive several agents

simultaneously, including the potent platelet GPIIb/IIIa receptor antagonists. It is estimated that 1% to 3% of patients
with an ACS will present with or develop GI bleeding during their index hospitalization.92-95 Patients who develop
GI bleeding in the setting of ACS have an almost 4- to 7fold increased risk of in-hospital mortality over patients
with ACS and no GI bleeding.93,94 In this context, clinicians
are faced with the dilemma with proceeding with endoscopic evaluation in a patient at an increased risk of procedural complications. Despite the clinical signicance of GI
bleeding during ACS, there are sparse data on outcomes of
patients with GI bleeding in the setting of ACS. In 1 retrospective case-control study, 200 patients underwent endoscopy within 30 days (mean, 9.1  8.9) of an acute MI.94
Serious adverse events (fatal ventricular tachycardia and
near respiratory arrest) occurred in 2 patients (1%). In
another study, ACS patients with an upper GI bleed were
associated with markedly increased mortality.96
Patients may develop an acute MI after a GI bleed,
and these patients are likely to benet from endoscopic
evaluation. A retrospective study showed that patients
who presented with upper GI bleeding leading to acute
MI were more likely to require endoscopic therapy
than patients who developed GI bleeding after being
treated for acute MI (OR 3.9; 95% CI, 1.8-8.5).95 Other
factors associated with the need for endoscopic therapy
included hemodynamic instability and hematemesis
on presentation. The benet of endoscopy in the
patient with signicant GI bleeding in the setting of
acute MI is supported by a decision analysis that
showed upper endoscopy before cardiac catheterization
to be benecial in patients who presented with overt
GI bleeding in the setting of ACS, reducing overall
deaths from 600 to 97 per 10,000 patients. However,
endoscopy was not found to be benecial in patients
who presented with occult GI bleeding and acute MI.97
Our understanding of the safety of endoscopy in
patients with ACS and/or recently placed intracoronary
stents on antithrombotic medications, including
DAPT and GPIIb/IIIa inhibitors, is rapidly evolving and
is likely to change as knowledge and experience are
accumulated.

RECOMMENDATIONS (SUMMARIZED
IN TABLE 13)
A. Elective endoscopic procedures
Patients receiving anticoagulant therapy
1. We recommend that elective endoscopic procedures be
deferred until short-term anticoagulation therapy (eg,
warfarin for VTE) is completed. 444B
2. We suggest discontinuing anticoagulation (ie, warfarin
[Coumadin], NOACs) for the appropriate drug-specic
interval in the periendoscopic period if high-risk
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Management of antithrombotic agents for patients undergoing GI endoscopy

TABLE 13. Management of antithrombotic agents in the elective endoscopic setting

Endoscopy-induced bleeding risk
Low
Low

High

AC

1. Continue warfarin and NOAC

AC

1. Discontinue AC
2. Restart warfarin on same day of procedure
3. Delay reinitiating NOACs until adequate hemostasis is achieved

APA

1. Continue standard doses of ASA/NSAIDs

2. Continue thienopyridines

APA

1. Continue standard doses of ASA/NSAIDs*

2. Discontinue thienopyridines at least 5 days before switch to ASAy
3. Dual APA, hold thienopyridines for at least 5 days, continue ASAy

AC

1. Continue warfarin and NOAC

AC

1.
2.
3.
4.

APA

1. Continue standard doses of ASA/NSAIDs

2. Continue thienopyridines

APA

1. Continue standard doses of ASA/NSAIDs

2. Discontinue thienopyridines at least 5 days before
endoscopy or switch to ASAy
3. Dual APA, hold thienopyridines for at least 5 days, continue ASAy

CV risk
High

Discontinue AC
Bridge therapyz
Restart warfarin on same day of procedure
Delay reinitiating NOACs until adequate hemostasis is achieved

AC, Anticoagulants; APA, antiplatelet agent; NOAC, novel oral anticoagulant; ASA, acetylsalicylic acid, or aspirin; NSAID, nonsteroidal anti-inflammatory drug; CV, cardiovascular.
*There is evidence to hold APA in patients undergoing ESD and EMR who have a low risk for a thromboembolic event.116
yTicagrelor should be held for 3-5 days, and all other thienopyridines should be held for 5-7 days.
zIn moderate-risk patients (from Table 5), the decision to use bridging therapy and the degree of intensity should be individualized and the patients wishes considered.40

3.

4.

5.

6.

1.

2.
3.

4.

endoscopic procedures are planned in a patient at low

risk for thromboembolic events. 44BB
We suggest continuing warfarin and NOAC in the periendoscopic period in patients undergoing low-risk
endoscopic procedures. 44BB
We suggest bridge therapy for patients undergoing
high-risk endoscopic procedures who are at high risk
for thromboembolic events. 44BB
We suggest that warfarin (Coumadin) be restarted on
the same day as the procedure in all patients who do
not have ongoing bleeding. 44BB
We suggest that the reinitiation of NOACs after high-risk
endoscopic procedures be delayed until adequate hemostasis is ensured, given their rapid onset of action
and lack of reversal agents. If therapeutic doses of
NOACs cannot be restarted within 12 to 24 hours after
a high-risk endoscopic procedure, thromboprophylaxis
(ie, UFH bridge) should be considered to decrease
risk of thromboembolism, given the short half-life of
the NOAC agent, in those with a high risk for thromboembolism. 44BB
Patients receiving APA therapy
We suggest that continuation of low doses of ASA and
nonsteroidal anti-inammatory drugs may be continued
safely in the periendoscopic period. 444B
We recommend that thienopyridines be continued for
all low-risk endoscopic procedures. 444B
We recommend discontinuation of thienopyridines at
least 5 to 7 days before high-risk endoscopic procedure
or switching to ASA monotherapy and continuing until
the thienopyridine can be safely resumed. 444B
We recommend that elective endoscopic procedures be
deferred in patients with recently placed intracoronary
stents and/or ACS until the patient has received

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antithrombotic therapy for the minimum recommended

duration. 444B
5. We suggest that thienopyridines be withheld for at least
5 to 7 days (ticagrelor 3-5 days) before high-risk endoscopic procedures and that ASA be continued for patients requiring dual APA. 444B

B. Urgent and emergent endoscopic

procedures
Patients receiving anticoagulant therapy
1. We recommend patients with acute GI bleeding on anticoagulation therapy have anticoagulant agents held to
facilitate achievement of hemostasis. 444B
2. We recommend either (1) 4-factor PCC and vitamin K or
(2) fresh frozen plasma be given for life-threatening GI
bleeding in patients on warfarin anticoagulant therapy.
Please note the ACCP only advocates option 1. The
AHA/ACC supports option 1 or 2. 444B
3. We suggest endoscopic therapy not be delayed in patients with serious GI bleeding and an INR < 2.5.
44BB
4. We suggest patients who require anticoagulation receive
UFH because of its relatively short half-life after successful endoscopic hemostasis for high-risk stigmata.
44BB
Patients receiving APA therapy
1. We recommend consultation with the prescribing
specialist (or their colleague) before stopping APAs in
situations of signicant GI bleeding in patients (1)
with recently (<1 year) placed drug eluting intracoronary stents, (2) within 30 days after insertion of a bare
metal intracoronary stent, or (3) within 90 days of
ACS. The risk of an adverse cardiac event associated
Volume 83, No. 1 : 2016 GASTROINTESTINAL ENDOSCOPY 13

Management of antithrombotic agents for patients undergoing GI endoscopy

with cessation of the APA therapy likely exceeds the

benet of decreasing postendoscopic bleeding. 444B
2. We recommend patients on APAs with life-threatening
or serious GI bleeding should have these agents held after discussion with their cardiologist. 444B

DISCLOSURE
The following authors disclosed nancial relationships
relevant to this publication: K. V. Chathadi is a consultant
for Boston Scientic. J. H. Hwang is a speaker for Novartis, a consultant for US Endoscopy, and has received a
research grant from Olympus. M. A. Khashab is a consultant for Boston Scientic and Olympus America, and has
received a research grant from Cook Medical. All other
authors disclosed no nancial relationships relevant to
this publication.
Abbreviations: ACS, acute coronary syndrome; AF, atrial brillation;
APA, antiplatelet agent; ASA, acetylsalicylic acid, or aspirin; CVA,
cerebrovascular accident; DAPT, dual antiplatelet therapy; DVT, deep
vein thrombosis; FDA, U.S. Food and Drug Administration; GP,
glycoprotein; INR, International Normalized Ratio; LMWH, lowmolecular-weight heparin; MI, myocardial infarction; NOAC, novel
oral anticoagulant; PAR-1, protease-activated receptor-1; PCC,
prothrombin complex concentrate; UFH, unfractionated heparin; VTE,
venous thromboembolism.

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