Transcript
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HARVARD MEDICAL SCHOOL

CaseBasedInterventionalCardiology

TeachingforthePCP

UpdateinInternalMedicine

DuanePinto,MD,MPH,FACCCOPYRIGHT

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HARVARD MEDICAL SCHOOL

Agenda

• IntroductiontotheCathLab

• Whattypesofproceduresaredoneinacath lab

• ConsiderationsforPCPbeforeandafterinterventional

procedures

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HARVARD MEDICAL SCHOOL

WhatProceduresDoneintheCardiacCathLab

• Coronaryangiographyandrevascularization

• Hemodynamicstudies

– Valveinterrogation

– Heartfailure/PericardialConstriction

– Pulmonaryhypertensionevaluation

• Structuralheartprocedures

– ASD/PFO/PDA/Paravalvularleak

– EthanolablationforHOCM

– TranscatheterAVR

– TranscatheterMitralandTricuspidValve

repair/replacement

– Appendageclosure

• Mechanicalassistdevicesforshock

• Peripheralrevascularizationstudies/IVCFilter

insertion/removal

• Pericardialtap/balloonostomy

• EndomyocardialBiopsies

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HARVARD MEDICAL SCHOOL

RHC

• Pressuremeasurements

–Valvularheartdisease

–FillingPressures

–Pulmonaryhypertension

–Pericardialprocesses/Restriction

• OximetricMeasurements

–Shunts

–Cardiacoutput- FickEquation

–Resistances- Ohm’sLaw

4

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HARVARD MEDICAL SCHOOL

RHC

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HARVARD MEDICAL SCHOOL

DetectingShuntsbyOxymetry

∆mean ∆highest QP/QS

Site Sat% Sat% threshold

ANY (PA from SVC) ≥7 ≥8 1.5

RA (from SVC/IVC) ≥7 ≥11 1.5-1.9

RV (from RA) ≥5 ≥10 1.3-1.5

PA (from RV) ≥5 ≥5 1.3

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HARVARD MEDICAL SCHOOL

AtrialTracings

Chest 2000; 118:1788-91.

JVPx

x+x’y

v

ca

x’

S1 S1 S2S2

RA

a c

x’

vx

y

a v

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HARVARD MEDICAL SCHOOL

Case:ET

Severe mitral regurgitation

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HARVARD MEDICAL SCHOOL

TheWorldChangedforFunctionalMRon9/23/18

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HARVARD MEDICAL SCHOOL

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HARVARD MEDICAL SCHOOL

ExerciseHemodynamics

• Forevaluationofvalvulardiseaseandothersituations

• SimultaneouscatherizationisdoneandpressuremeasurementsofRT&LTheartistaken–Atrest

–Withexertion

• Catheterisplacedin:–Anartery(femoralorbrachial)

–Vein(femoralorbasilic)

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HARVARD MEDICAL SCHOOL

AdvancedDiagnosticStudiesoftheVascularSystem

• BiopsycatheterwithbioptometipisinsertedintojugularorfemoralveinintoRTventricle

• Jawsareopenedandmanybiopsiesaretaken

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HARVARD MEDICAL SCHOOL

BioptomeBiopsies

• Usedtomonitorcardiac

transplantsfortissuerejection

• Andtodifferentiatebetween

varioustypesofcardiomyopathies

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HARVARD MEDICAL SCHOOL

RadialSheath

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HARVARD MEDICAL SCHOOL

Rate Ratio 0.83; 95% CI, 0.73 to 0.96; p=0.0092

11.7%

9.8%

NNTB: 53FemoralRadial

Primary EP: NACE

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HARVARD MEDICAL SCHOOL

CoronaryAngiography

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HARVARD MEDICAL SCHOOL

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HARVARD MEDICAL SCHOOL

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HARVARD MEDICAL SCHOOL

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HARVARD MEDICAL SCHOOL

67Yearoldwomanwithchestpain

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HARVARD MEDICAL SCHOOL

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HARVARD MEDICAL SCHOOL

Ididn ttellyouthewholestory…..

Thatwas23yearsago.Nowsheis90andin

shockwithSTEMI

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HARVARD MEDICAL SCHOOL

• Myleftarmwascoldallofthetime!

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• RecoveredfromMI,ShockandATN

• Dischargedto12dayslater

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DurationofDAPT

• Dualantiplatelettherapy(ASAandP2Y12)isusedforsecondary

preventionofvasculardiseaseandtopreventdevice

thrombosis

• DAPTismandatoryforaperiodoftimewithoutinterruptionto

preventstentthrombosis.

–Peripheralvascularstents1month

–Percutaneousvalves3monthsunlessbleedingorneedanticoagulation

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HARVARD MEDICAL SCHOOL

InpatientswithACS(STEMIorNSTEACS)whoreceivePCI:

Values and Preferences: These recommendations place greater emphasis on reduction of major cardiovascular events and stent thrombosis versus an increase in bleeding complications.

Recommendations

• We recommend dual antiplatelet therapy (DAPT) with ASA 81 mg daily plus either ticagrelor 90 mg twice daily or prasugrel 10 mg once daily over clopidogrel 75 mg once daily for 1 year (Strong

Recommendation, High Quality Evidence).

• We recommend that in patients who tolerate 1 year of DAPT without a major bleeding event and who are

not at high risk of bleeding, DAPT should be extended beyond 1 year (Strong Recommendation, High Quality Evidence for up to 3 years of treatment). After 1 year, we recommend a DAPT regimen of ASA 81 mg daily plus either ticagrelor 60 mg twice daily or clopidogrel 75 mg once daily (Strong

Recommendation, High Quality Evidence) or prasugrel 10 mg once daily (Weak Recommendation, Moderate Quality Evidence).

2018 CCS/CAIC Focused Update of the Guidelines for the Use of Antiplatelet Therapy

https://www.ccs.ca/images/Guidelines/Educational.../APT_Gui_2018_SD_EN.pptx

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HARVARD MEDICAL SCHOOL

DurationofDAPTforpatientstreatedwithPCIinACS

settings

Practical tips:

• Recommendations on duration of DAPT apply specifically to duration of P2Y12 inhibitor

therapy. ASA should be continued indefinitely in most patients with CAD who are not on oral

anticoagulant therapy.

• Patients who have clinical or angiographic features for an increased risk of a thrombotic

cardiovascular event may derive greater absolute benefit from extended DAPT beyond 1 year.

• Quantitative risk scores have been developed. These scores may help identify higher risk

patients with greater absolute benefit of extended DAPT .

• An ongoing assessment of bleeding and ischemic risk should be performed at least annually to

determine whether DAPT should be continued.

• Prasugrel should be avoided in patients with previous TIA or stroke.

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HARVARD MEDICAL SCHOOL

PCI for STEMI or NSTEACS

DAPT for 1 year

ASA 81 mg once daily +

Ticagrelor 90 mg BID or Prasugrel 10 mg once daily preferred over

Clopidogrel 75 mg once daily

At 1 year, determine bleeding risk

Not at high risk of bleeding1

1 Factors associated with increased bleeding risk include: need for OAC in addition to DAPT,

advanced age (> 75 years), frailty, anemia with hemoglobin < 110 g/dL, chronic renal failure

(creatinine clearance < 40 mL/min), low body weight (< 60 kg), hospitalization for bleeding within

last year, prior stroke/intracranical bleed, regular need for NSAIDS or prednisone2 Instead of ticagrelor or clopidogrel, prasugrel 5-10 mg daily is also an option (weak

recommendation)

DAPT=dual antiplatelet therapy SAPT=single antiplatelet therapy STEMI=ST segment elevation

myocardial infarction NSTEMI=non-ST segment elevation myocardial infarction BID=twice daily

Strong recommendation

Weak recommendation

High risk of bleeding1

Continue DAPT for up to 3 years

ASA 81 mg once daily +

Ticagrelor 60 mg BID or

Clopidogrel 75 mg once daily2

SAPTASA 81 mg once daily

orClopidogrel 75 mg once daily

2018 CCS/CAIC Focused Update of the Guidelines for the Use of Antiplatelet Therapy

https://www.ccs.ca/images/Guidelines/Educational.../APT_Gui_2018_SD_EN.pptx

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Clinical AngiographicPriormyocardialinfarctionortroponin

positiveacutecoronarysyndrome

Multiplestents(≥3stentsimplanted,≥

3lesionsstented)

DiabetesMellitustreatedwithoral

hypoglycemics orinsulin

Longlesionlength(>60mmtotalstent

length)

Chronickidneydisease(creatinine

clearance≤60ml/min)

Complexlesions(bifurcationtreated

with2stents,stentingofchronic

occlusion)

Priorstentthrombosis LeftmainorproximalLADstenting

Multivessel PCI

Net benefit to diabetics in the absence of any of other high risk features is unclear

High-riskclinicalandangiographic featuresfor

thromboticevents

2018 CCS/CAIC Focused Update of the Guidelines for the Use of Antiplatelet Therapy

https://www.ccs.ca/images/Guidelines/Educational.../APT_Gui_2018_SD_EN.pptx

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HARVARD MEDICAL SCHOOL

Factorsassociatedwithincreasedbleeding risk

1. Need for OAC in addition to DAPT

2. Advanced age (> 75 years)

3. Frailty

4. Anemia with hemoglobin < 110 g/dL

5. Chronic renal failure (creatinine clearance < 40 mL/min)

6. Low Body Weight (< 60 kg)

7. Hospitalization for bleeding within last year

8. Prior stroke/intracranical bleed

9. Regular need for NSAIDS or prednisone

2018 CCS/CAIC Focused Update of the Guidelines for the Use of Antiplatelet Therapy

https://www.ccs.ca/images/Guidelines/Educational.../APT_Gui_2018_SD_EN.pptx

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HARVARD MEDICAL SCHOOL

RiskscoresforDAPTdurationdecisions

Score Name Online calculator Patient Population Score Description DAPT

duration

periods

Score variables Validation Comments

PRECISE-

DAPT19

www.precisedaptsco

re.com/predapt/inde

x.html

PCI with or without

ACS

Estimates 1 year rates of ischemic and

bleeding events for patients treated with

PCI.

Patients with PRECISE-DAPT score>25

have lower predicted rates of bleeding

events and similar rates of ischemic

events with shortened DAPT (3-6

months versus 12-24 months)

3-6 months

vs. 12-14

months

Age, previous bleeding,

white- blood-cell count,

haemoglobin, creatinine

clearance

Validated in two separate

cohorts (total patients

involved in the development:

29,730)

c-statistic in the two

validation cohorts = 0.66 and

0.70

Discrimination lower for patients on

prasugrel

Angiographic and PCI variables not included

Does not provide guidance to support the

decision to prolong DAPT over one year

following PCI

CALIBER130 https://farr-data-

lab.shinyapps.io/cali

ber-

prolonged_dapt_ben

efits_harms_risks/

Patients surviving 1

year post MI including

those treated with or

without PCI

Estimates ischemic and bleeding events

2-6 years post MI with and without

prolonged DAPT

12 months

vs. >12

months

Ischemic prediction score

includes 20 variables and

bleeding prediction score

includes 18 variables

Validated in two cohorts

(total patients involved in the

development: 19,784)

c-statistic in the validation

cohort = 0.75 for ischemic

endpoints, and 0.72 for

major bleeding

High number of variables included in the

model

Angiographic and PCI variables not included

Did not include any patients treated with

prasugrel

DAPT16 http://tools.acc.org/

DAPTriskapp/#!/co

ntent/calculator/

Patients 1 year after

PCI without bleeding

or ischemic events

Estimates the net benefit between

ischemic and bleeding events with

prolonged DAPT. Patients with DAPT

score ≥ 2 had fewer ischemic and

bleeding events with prolonged dual

antiplatelet therapy (>12 months)

12 months

vs. >12

months

Age, cigarette smoking,

diabetes mellitus, MI at

presentation, prior PCI or

prior MI, paclitaxel-

eluting stent, stent

diameter <3 mm, CHF or

LVEF <30%, vein graft

stent

Validated in a separate

retrospective cohort (total

patients involved in the

development: 19,784)

c-statistic in the validation

cohort = 0.64 in both the

ischemic and bleeding

models

Incorporates angiographic and PCI data

<50% of the patients in the derivation cohort

were implanted second-generation DES

Did not include any patients treated with

ticagrelor

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History

• 72yearoldwomanwithdiabetes underwent19mmtissue AVR.25mmtissueMVR

andtricuspid valverepairwitha28mmPhysio IIannuloplasty ringin11/16for

radiation inducedvalvedisease (Hodgkin’s)withSVGtoRCA

• Overthenext2months,describes Class III-IVsymptomsoffatigue,abdominal

fullness andedema

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Recovery

• Postprocedurerecoverycomplicated bychylothorax unrelated toTTVRaccess

• 6monthfollow-up,rightsided symptomsresolved,Class IIsymptomsthoughtrelated

todiastolic heartfailuremanagedwithdiuretics

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4monthfollow-upECHO

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EndocarditisProphylaxisandfollow-up

• Noneedforcoronaryandperipheralstents

• ASD/PFOClosure=6months

• Trancatheter valves-=Lifelong

• ECHOinhospital,30days,yearlyCOPYRIGHT

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•89yearoldmanwithLVEF20-25%,ASwithpeak

gradient28mmhg,Mean15mmHg,CABG2002

referredforelectivePCIaftercatheterizationfor

medicationveryabnormalstresstestpriorto

urologicsurgeryCOPYRIGHT

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Elective PCI

Not at high risk of bleeding1 High risk of bleeding1

DAPT for 6 months

ASA + clopidogrel

YES

1 Factors associated with increased bleeding risk include: need for OAC in addition to DAPT, advanced age (> 75 years), frailty, anemia with hemoglobin < 110 g/dL, chronic renal failure (creatinine clearance < 40 mL/min), low body weight (< 60 kg), hospitalization for bleeding within last year, prior stroke/intracranical bleed, regular need for NSAIDS or prednisone.

2 Clinical and angiographic features associated with increased risk of thrombotic events include: age > 65, diabetes mellitus, prior myocardial infarction, chronic renal dysfunction (creatinine clearance < 60 mL/min), multi-vessel disease, multiple stents implanted, complex bifurcation lesion, total stent length > 60 mm, chronic total occlusion intervention or bioabsorbable vascular scaffold (BVS) implantation.

DAPT=dual antiplatelet therapy SAPT=single antiplatelet therapy BMS=bare metal stent DES=drug eluting stent

High-riskclinical or angiographic featuresfor thrombotic cardiovascular events2,

and not at high risk of bleeding?1

DAPT for 1 month if BMS,

or 3 months if DES

NO

Extend DAPTup to 3 years

ASA 81 mg daily +

Clopidogrel75 mg daily

SAPT

ASA 81 mg daily or

Clopidogrel75 mg daily

Strong recommendation

Weak recommendation

SAPT

ASA 81 mg daily or

Clopidogrel

75 mg daily

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InterruptingDAPTfornon-cardiacsurgery

• In patients treated with a bare metal stent who require elective non-cardiac

surgery, we recommend delaying surgery for at least 1 month after PCI

(Strong Recommendation, Moderate Quality Evidence).

• In patients treated with a drug eluting stent who require elective non-cardiac

surgery, we recommend delaying surgery for at least 3 months after PCI

(Strong Recommendation, Moderate Quality Evidence). If there is a need

for semi-urgent non-cardiac surgery, we suggest delaying surgery for at least

1 month after PCI (Weak Recommendation, Low Quality Evidence).

Recommendations

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InterruptingDAPTfornon-cardiacsurgery

• In patients treated with a bare metal or drug eluting stent who require elective non-cardiac

surgery, we suggest continuing ASA perioperatively whenever possible (Weak

Recommendation, Low Quality Evidence).

• In patients treated with a bare metal or drug eluting stent who require elective non-cardiac

surgery, we suggest withholding clopidogrel and ticagrelor for 5-7 days pre-operatively, and

prasugrel for 7-10 days pre-operatively (Weak Recommendation, Low Quality Evidence).

• In patients treated with a bare metal or drug eluting stent who have undergone non-cardiac

surgery, we suggest restarting maintenance dose DAPT after surgery, as soon as it is

deemed safe by the surgeon (Weak Recommendation, Very Low Quality Evidence).

Recommendations

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InterruptingDAPTfornon-cardiacsurgery

Practical tip:

• The risk and consequences of peri-operative bleeding will vary

considerably depending on the type of surgery performed. Some minor

surgical procedures carry a low risk of bleeding, while others a very high

risk of bleeding. For example, some dental, opthalmological and

endoscopic procedures carry a low risk of bleeding and can be performed

without stopping antiplatelet therapy.COPYRIGHT

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Follow-up

• ImprovedLVfunctiononf/uECHO

• Nofurtherangina

• Uncomplicatedbladdersurgery3monthslateron

aspirin

• Continuesmedicalmanagement15monthfollow-upCOPYRIGHT

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74 year old woman with

diabetes, hypertension,

atrial fibrillation had

cardiac arrest and is

now recovered after PCI

of left main COPYRIGHT

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Dual Pathway Triple Therapy

1. Rivaroxaban 15 mg once daily + clopidogrel

75 mg once daily1

1. Rivaroxaban 2.5 mg BID + ASA 81 mg once

daily + clopidogrel 75 mg once daily1

2. Dabigatran 110* or 150 mg BID + clopidogrel

75 mg once daily2

2. Warfarin (INR 2.0-2.5) + ASA 81 mg once

daily + clopidogrel 75 mg once daily4

3. Warfarin + clopidogrel 75 mg once daily3

Dual Pathway and Triple Therapy Regimens

Evaluated in Clinical Trials

1. PIONEER-AF: Gibson CM etal. NEJM2016;375:2423]

2. RE-DUAL PCI: Cannon CP eta.l. NEJM2017; 377:1513-1524

3. WOEST: Dewilde etal.,Lancet 2013;381:1107-15

4. ISARTriple :Fiedler etal.JAmColl Cardiol 2015;65:1619-29

*IntheRE-DUALPCI trial,the110mgBIDdabigatrandosewasassociatedwithatrendtoahigherriskofdeathorthromboticevents(11%versus 8.5%,hazardratio1.30,95%CI0.98-1.73, P=0.07). This riskwasnotobservedwiththe150mgBIDdose (7.9%versus 7.9%,hazardratio0.97,95%CI0.68-1.39, P=0.44). Therefore,in

patientswho arenotathighriskofbleeding,thedabigatran150mgBIDdose,whenused incombinationwithclopidogrel 75mgdaily(ASAomitted),maybe

preferable.

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DifferingOACregimens inpublished randomizedtrialsof

patientswithAFundergoingPCI

Trials Studiedregimens Primaryendpoint Comments

WOEST(n=573)

Lancet 2008

Warfarin(targetINR2.0)+clopidogrel75mgdaily

Versus

Warfarin(targetINR2.0)+clopidogrel75mgdaily+ASA80-100mgdaily

Anybleedingepisodeat12months

Warfarin+clopidogrel:19.4%

Warfarin+clopidogrel+ASA:44.4%

(p<0·0001)

PrevalenceofAF/flutter:69%

Useof PPI:<40%

Stentsused65%DES,35%BMS

ISAR-TRIPLE(n=614)

JACC2015

ASA75-200mgdaily

+clopidogrel75mgdaily

+warfarin(lowestrecommended targetINR)

for6weeksversus6months

Composite ofdeath,MI,definitestentthrombosis,stroke,or

majorbleedingat9months

•6weekstripletherapy:9.8%

•6months tripletherapy:8.8%(p=0.63)

PrevalenceofAF:84%

Useof PPI:37.2%

Stentsused99%DES

INRtherapeuticrange64%

PIONEER-AF(n=2124)

NEJM2016

Rivaroxaban15mgdaily+P2Y12inhibitor(group1)

vs

Rivaroxaban2.5mgtwicedaily+DAPT(group2)

vs

Warfarin(INR 2.0-3.0) +DAPT(group3)

Clinicallysignificantbleedingat12months

Group1:16.8%

Group2:18.0%

Group3:26.7%(p<0.001 versusbothgroups 1and2)

PrevalenceofAF:100%

Clopidogrelused in93%ofpatients

Useof PPI:<40%

Stentsused65%DES,32%BMS

INRtherapeuticrange65%

RE-DUALPCI(n=2725)

NEJM2017

Dabigatran 110mgtwicedaily+P2Y12inhibitor(clopidogrel75mgdaily

orticagrelor 90mgtwicedaily)

vs

Dabigatran 150mgtwicedaily+P2Y12inhibitor(clopidogrel75mgdaily

orticagrelor 90mgtwicedaily)

vs

Warfarin(INR 2.0-3.0) +P2Y12inhibitor(clopidogrel75mgdailyor

ticagrelor 90mgtwicedaily)+aspirin£100mgdaily

Timetofirstmajororclinicallyrelevantnon-majorbleeding

event

15.4%in110mgdualtherapyvs26.9%comparabletriple

therapygroup(P<0.001for noninferiority;P<0.001for

superiority)

20.2%in150mgdualtherapyvs25.7%comparabletriple

therapygroup(P<0.001for noninferiority)

PrevalenceofAF:100%

Clopidogrelused in88%ofpatients

Stentsused83%DES,35%BMS

Useof PPI:unknown

INRtherapeuticrange64%

Randomized Trials of OAC Following PCI

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Whatifpatient’scan’ttakeanticoagulationforAF:

ConsiderationforLAAClosure

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Summary

• Thecardiaccatheterizationlaboratoryof2018providesawidevarietyof

servicesincludingdiagnostictestingforcoronary,valvular,myopathic,

pericardialandpulmonicdisorders

• Therapeuticinterventionsincludecoronaryrevascularization,valve

replacementandrepair,peripheralarterialrepair,mechanicalsupport

devices,anddefectclosure

• CommonconsiderationsforthePCPincludedurationofDAPT,

anticoagulationdecisionsparticularlyaroundprocedures,endocarditis

prophylaxisandsecondarypreventionofCADandCHF

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