coronary syndrome MUDr Denisa Jahnlová Department of Cardiology FN Motol and 2nd Medical Faculty of the Charles University Acute coronary syndromes Pathophysiologic ID: 918561
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Slide1
Treatment of acute coronary syndrome
MUDr. Denisa JahnlováDepartment of CardiologyFN Motol and 2nd Medical Faculty of the Charles University
Slide2Acute coronary syndromes
Pathophysiologic mechanismvulnerabile plaque disruption with superimposed thrombus and subsequent coronary blood flow cessation
with reduced myocardial
supply
→ acute ischemia → necrosisLeading symptom - chest pain2 groups according to ECGPatients with acute chest pain and persistent (20 min) ST-segment elevationThis condition is termed ST-elevation ACS and generally reflects an acute total coronary occlusionMost patients will ultimately develop an ST-elevation myocardial infarction (STEMI)Immediate reperfusion by primary angioplasty or fibrinolytic therapyPatients with acute chest pain but no persistent ST-segment elevationECG changes may include transient ST-segment elevation, persistent or transient ST-segment depression, T-wave inversion, flat T waves or pseudo-normalization of T waves or the ECG may be normalNSTEMI - myocardial necrosisNAP - myocardial ischemia without cell loss, lower risk of death
Slide3Slide4Slide5Slide6EpidemiologyIncidence of NSTEMI higher than incidence of STEMI
In-hospital mortalityHigher in STEMI patients vs. NSTEMI (7 vs. 5%)STEMI - mortality 25-30% (1960s) → 10% (nowadays)6 month mortalitySimilar in both groups (12 vs. 13%)Long-term follow-up Higher in NSTEMI patientsOlder
patientsComorbidities (diabetes mellitus, renal insuficiency)
Generalized
atherosclerosis including multivessel
coronary diseaseSex differences men account for more than 90% of patients with AMI at the age under 40y (a hormonal profile of woman has a protective effect)Age differences in patients aged under 40 years only one coronary artery is affected
Slide7Slide8ACS with ST-segment elevationPre-hospital management
Relief of BreathlessnessO2 only to breathless, hypoxic (SaO2<95%), heart failure patient
Relief of painh
uman
reasons, sympathetic activation-vasoconstiction, increases workload of the hearttitrated i.v. opioids (Morphine, Fentanyl) + antiemeticsRelief of anxietyexplain the situation to the patient, tranquillizerBBhypertensive and tachycardic patient metoprolol, bisoprolol, esmololCAVE contraindication: acute cardiac failure, bradycardia
Slide9ACS with ST-segment elevationPre-hospital management
Nitrate pain, hypertesion, heart failuresublingual, intravenous
(isosorbide dinitrate
1-5 mg i.v.
in hypertensive
patients) CAVE! Contraindications: hypotense, sildenafil → resistent hypotension Monitoring vital function and ECGCardiac arrest due to ventricular fibrillation!!!Terminated by defibrillationTheapeutic hypothermia after resuscitation is indicatedImmediate angiography in patients with CA whose ECG shows STEMI/high suspicion on ongoing infarction
Slide10ACS with ST-segment elevation Reperfusion therapy: time is muscle!!!
Indication within 12 h of symptom onset with persistent STE or new LBBB (later → necrosis)in patients
with ongoing ischemia
→
laterwithin 120 minutes of first contact with doctorTypes of RTmechanical (PCI)preferred reperfusion strategy randomized clinical trials → superior to fibrinolysispharmacological (fibrinolysis)
Slide11Prehospital and in-hospital management
Slide12Reperfusion Strategy in Europe
Reperfusion therapy 37-93%pPCI rate varies
between 5 and 92%;
Thrombolysis
0-55%
EUROPE IS VERY HETEROGENOUS!!!
Slide13≥600 p-PCI /
million
/
year
400-599 p-PCI /
million
/
year
200-399 p-PCI /
million
/
year
<
200 p-PCI /
million
/
year
Data not
known
Annual
I
ncidence
of
P
rimary
PCIs
Slide14The distribution of the 22
interventional centers working (24/7) in the Czech RepublicPopulation of the Czech Republic is 10 million
people
Slide15ACS with ST-segment elevation Mechanical
reperfusion therapy - PCIPrimary PCI (pPCI) is reccomended over fibrinolysis within 120 minutes of FMC In unstable patients (acute heart failure/cadiogenic shock) unless related delayStenting (new generation of DES) + tromboaspiration is recommended balloon angiopasty alone
Radial access should be prefered over femoral
access
reduces
incidence of acute bleeding events (RIVAL trial)pPCI should be limited to the culprit vessel except of patients in cardiogenic shock and persistent ischemia after PCI
Slide16Process
of the implantation of stent
Slide17Aspiration trombectomy
Slide18Slide19ACS with ST-segment elevationIn-hospital care
– periprocedural pharmacotheraphyDAPT -combination of aspirin + ATP inhibitorsAspirin For all patients without contraindicationsInitial oral loading dose 150-300 mg, 75-100 mg daily
ATP inhibitorsIn addition to Aspirin for 12 months unless contraindications3-6 months afted DES implantation in case of high bleeding risk
Ticagrelor
180 mg loading dose, 90 mg twice daily in all patients with high or intermmidiate ischemic risk
Prasugrel 60 mg loaging dose, 10 mg daily dosecontraindicated in patients with prior stroke and older > 75y. and body weight <60 kgClopidogrel300-600 mg loaging dose,75 mg daly doseOnly in patients who cannot recieve ticagrelor or prasugrel or who require oral antikoagulationPPI inhibitors in patients in risk of gastrointestinal bleeding
Slide20ACS with ST-segment elevationIn-hospital
care – periproceduralpharmacotheraphyUnfractionated heparin (UFH) in patients undergoing PCI70-100 IU/Kg i.v. (max.5000 IU bolus before
PCI)APTT 1,5-2,5xLMWH (low
molecular
weight heparin)0,5 mg/kg i.v. followed by 1 mg/kg s.c.Fondaparinux is not recommended!Glykoprotein IIb/IIIa inhibitorsBailout therapy - only in no-reflow, massive trombus, trombotic complicationsOnly periprocedural!!!
Slide21ACS with ST-segment elevation Pharmacological
reperfusion therapy: FibrinolysisFibrinolysis is an important in those settings where primary PCI cannot be offered to STEMI patients within the recommended timelinesHigher risk of
bleeding, sucesfull
only
in 70-80%
Within 12 h of symptom onset if primary PCI cannot be performed within 120 minPrehospital startA fibrin-specific agent (tenecteplase, alteplase, reteplase) is recommendedAnticoagulation (UFH/enoxaparin) is recommended until revascularization and for the duration of hospital stayDAPT (aspirin + clopidogrel)Transfer to a PCI-capable centre is indicated for all patients following fibrinolysis
Unstable
patients
-
rescue
/
emergency
PCI
Stable
patients
– PCI in 3-24 hod
Slide22Slide23Fibrinolysis x PCIMeta-analysis of
23 trials (n=7739 pts.)
Keeley
EC. Lancet 2003
Slide24ACS with ST-segment elevation Management during
hospitalizationThe Coronary Care Unit Management of arrhythmias, heart failure, mechanical circulatory support and complex (non)invasive and haemodynamic monitoring
Patients should stay on coronary care unit
for
2-3 days (at least 24 hours)Standard cardiology departmentEven after leaving the CCU patients are able to move around the room and in the following days rehabilitate and before discharge they are able to walk up the stairsThe total length of hospitalization is around 1 weekReturn to job possible approximately one month after the onset of the symptoms
Slide25ACS with ST-segment elevation Management at discharge
Low-risk patients with successful pPCI could safely be discharged from hospital at day 3 age <70 yearsLVEF > 45% 1 or 2 VDsuccessful PCIno persistent arrhythmias
Slide26ACS with ST-segment elevation Long-term therapies
CAD is a chronic condition and patients who have recovered from a STEMI are at high risk for new events and premature death !!!Most patients with STEMI who die do so after discharge from the index event!
Slide27ACS with ST-segment elevation Long-term therapies- l
ifestyle interventions and risk factor controlcessation of smokingtight blood pressure controldiet and weight controlthe encouragement of physical activity
Slide28ACS with ST-segment elevation Long-term therapies-
pharmacotherapyAntithrombotic therapy DAPT (combination of aspirin + ADP-receptor blocker) for up to 12 months
Aspirin indefinitely (75-100mg)
Tigagrelor
/
prasugrel is reccomended over clopidogrel for 12 monthsBeta-blockers In all patients without contraindications, especially in patients with heart failure and systolic dysfunctionMetoprolol up to 200 mg daily, Carvediol up to 25 mg daily, Bisoprolol up to 10 mg dailyContraindication: in patients in acute phase and heart failure, cardiogenic shock, bradycardiaStatins Lipid-lowering therapyAtorvastatin 40-80 daily, Rosuvastatin 20-40 mg dailyACE inhibitors In all patients without contraindications, especially in heart failure, left ventricular systolic dysfunction, diabetes mellitusRamipril 1,25 mg, Lisinopril 2,5 mg, Enalapril 2,5 mgIn case of intolerance : Valsartan 20 mg twice daily, Losartan, Candesartan is an alternative
Slide29ACS without ST-segment elevation
Patients with acute chest pain but no persistent ST-segment elevationECG changes may include transient ST-segment elevationpersistent or transient ST-segment depressionT-wave inversionflat T waves pseudo-normalization of T waves ECG may be normalThe clinical spectrum of non-ST-elevation ACS (NSTE-ACS) may range from patients free
of symptoms at presentation individuals with ongoing ischaemia
electrical
or haemodynamic instability
cardiac arrestThe pathological correlate at the myocardial level isNSTE-myocardial infarction (NSTEMI)- positive hsTnI, cardiomyocyte necrosisunstable angina –myocardial ischaemia without cell loss, negative hsTnI
Slide30ACS without ST-segment elevationOngoing ischemia
Patients may present with ongoing myocardial ischaemia, characterized by one or more of the following:recurrent or ongoing chest painmarked ST depression on 12-lead ECGheart failure haemodynamic or electrical instabilityImmediate PCI is indicateddue to the amount of myocardium in danger and the risk of malignant ventricular arrhythmias
Slide31ACS without ST-segment elevation- Risk score
and bleeding risk assesmentGrace risk scoreEstimenate the
in-hospital mortality,
mortality
at 6 months, at 1 year and at 3 years
The combined risk of death or MI at 1 yearVariables :ageSystolic blood pressurepulse rateserum creatinine Killip class at presentationcardiac arrest at admissionelevated cardiac biomarkers and ST deviationCrusade bleeding riskEstimate the patient’s likelihood of an in-hospital major bleeding eventbaseline patient characteristicsfemale genderhistory of diabeteshistory of peripheral vascular disease or strokeadmission clinical variables heart ratesystolic blood pressuresigns of heart failureadmission laboratory values haematocritcalculated creatinine clearance
Slide32ACS without ST-segment elevation Pharmacological treatment of ischaemia
Decrease myocardial oxygen demand or increase myocardial oxygen supplyO2only in patients with saturtion less than 90%/in respiratory distressBeta-blockers in patients
with ongoing ischaemic symptoms and without contraindications
N
itrates
i.v. or sublingual to relieve angina, uncontrolled hypertension or signs of heart failureCAVE! Avoid in patients with recent intake of sildenafilOpiatesonly in patients with symtoms despite the theraphy with BB and NitratesIf the patient is not free of signs and symptoms after this treament, immediate PCI is recommended!!!
Slide33ACS without ST-segment elevation Platelet
inhibition DAPT -combination of aspirin + ATP inhibitorsAspirin For all patients without contraindicationsInitial oral loading dose 150-300 mg, 75-100 mg dailyATP inhibitorsIn addition to Aspirin for 12 months unless contraindications3-6 months afted DES implantation in case of high bleeding risk
Ticagrelor 180 mg loading dose, 90 mg twice daily in all patients with high or intermmidiate ischemic risk
Prasugrel
60 mg loaging dose, 10 mg daily dose
contraindicated in patients with prior stroke and older > 75y. and body weight <60 kgClopidogrel300-600 mg loaging dose,75 mg daly doseOnly in patients who cannot recieve ticagrelor or prasugrel or who require oral antikoagulationPPI inhibitors in patients in risk of gastrointestinal bleeding
Slide34ACS without ST-segment elevation Anticoagulation
Unfractionated heparin (UFH) in patients undergoing PCI70-100 IU/kg i.v. (max. 5000 IU bolus berore PCI), APTT 1,5-2,5xFondaparinux The most favourable efficacy – safety profile in NSTEMIInhibition of Xa2.5 mg s.c. daily (CAVE renal insufficiency)OASIS-5 study – less bleeding eventsBolus UFH 70-85 IU/kg during the
procedure (to avoid formation of trombus on cathether) Low molecular weight heparin (LMWH)
In patients pretreated with LMWH
1 mg/kg twice daly (CAVE renal
insufficiency)Continuation after sucesfull PCI for 24 hin conservative treatment during hospital stay
Slide35ACS without ST-segment elevationR
eperfusion strategyPCI + implantation of stent (2nd generation DES) is the method of choiseTiming of PCI according to the risk stratificationFibrinolysis is not reccomended at NSTEMI
CABG (surgical revascularization) More frequently multivessel disease
with no culprit
lesion
Diabetic patientsHigher proportion of surgical high risk charakteristics (x elective CABG)Older ageFemale genderLeft main coronary diseaseLV dysfunctionHigher bleeding and ischemic risk (timing of surgery x DAPT)
Slide36ACS without ST-segment elevationTiming of reperfusion strategy
Slide37Slide38Slide39Slide40ACS without ST-segment elevation Long-term therapies
- pharmacotherapyAntithrombotic therapy DAPT (combination of aspirin + ADP-receptor blocker)
for up to 12 monthsAspirin indefinitely
(75-100mg
)
Tigagrelor/prasugrel is reccomended over clopidogrel for 12 monthsBeta-blockers In patients wih heart failure and systolic dysfunctionMetoprolol up to 200 mg daily, carvediol up to 25 mg daily, bisoprolol up to 10 mg dailyContraindication: in patients in acute phase and heart failureStatins Lipid-lowering therapyAtorvastatin 40-80 daily, Rosuvastatin 20-40 mg dailyACE inhibitors Heart failure, left ventricular systolic dysfunction, diabetes mellitusRamipril 1,25 mg, Lisinopril 2,5 mg, Enalapril 2,5 mg, Valsartan 20 mg twice daily, Losartan, Candesartan is an alternative when intolerance of ACEi is present