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88 Cards in this Set
- Front
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tecagrilor MoA
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reversible, non thienopyridine P2Y12 antagonist
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ticagrelor metabolism and activation
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CYP3A4
but NO hepatic activation (not prodrug?) |
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ticagrelor contraindications (3)
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hx of intracranial bleeds
severe hepatic dysfunction? CYP3A4 inhibitors or inducers |
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ticagrelor AE (2)
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bleeds (more than other thienopyridines)
dyspnea |
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goal of glycoprotein IIb/IIIa inhibitors
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prevent total occlusion of infarct related artery
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indication of glycoprotein IIb/IIIa inhibitors (2)
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to prevent ischemic complications FOLLOWING PCI
considered in pt with NSTE-ACS undergoing EI strategy (planned PCI) |
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usage of glycoprotein IIb/IIIa inhibitors- do you use it alone or in combo?
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DO NOT REPLACE anticoag- alsways use with LMWH/UFW otherwise you will increase mortality
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GP IIb/IIIa receptor function
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IIb/IIIa is for the actual clots- cross linking of fibrinogen
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how/when/duration to administer GP IIb/IIIa inhibitor after event
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continued 48-72 h after event or until PCI
if plavix loading (300 mg) was giving more than 6 h earlier you don't need to give GP inhibitors |
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3 GP IIb/IIIa inhibitors
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abciximab
tirofibane eptifibatide |
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difference in GP IIb/IIIa inhibitor usage in EI (2)
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abciximab or accelerated dose? epitifibatide if PCI is within 4h of presentation (or can get pt there in 4 h)
tirofiban or eptifibatide regular if treated medically for first 48 h |
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usage of GP IIb/IIIa inhibitors in EC: what patient population (type)
not beneficial where? |
use limited to those at high risk for future cardiac events (+troponin)
not really beneficial in EC strategy- particularly, abciximab is NOT USED in EC at all |
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ONLY use GP IIb/IIIa in EC if what 3 properties? (3)
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ONLY if continuing ischemia, +troponins, or TIMI risk >=4
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dosing (route)/2 drugs for GP IIb/IIIa inhibitors used in EC
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continuing infusion of tirofiban or eptifibatide
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abciximab- type of inhibitor
indication |
irreversible
PCI ONLY |
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abciximab- CL
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monoclonal...RES? (phagocytic cells?)
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eptifibitide- type of inhibitor
indication (2) |
reversible
UA/NSTEMI EC and ELECTIVE PCI |
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eptifibitide CL
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renal
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tirofiban CL
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renal
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tirofiban type of inhibitor
indication |
reversible
UA/NSTEMI EC |
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HR goal of BBs
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goal of BBs: slow heart rate to 55-60 BPM
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beta blocker- immediate treatment
then afterwards dosing |
metoprolol 5 mg IV q5min for 3 doses (immediate) IVP
then 25-50 mg po bid and increase as tolerated FOREVER. IS THIS TARTRATE? YES. OK. |
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benefits of BB in ACS (2)
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decreases risk of progression to AMI in pt with UA
reduces frequency of recurrent MI |
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mortality benefit with immediate IV therapy of BB
mostly used for hwat (2) |
no mortality benefit in NSTE-ACS with immediate iV therapy- mostly used for pt who are hypertensive or in afib with RVR
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BBs to avoid
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ones with ISA like acetobutolol
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absolute CI for BBs (7)
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HR < 55-60
SBP < 90-100 mod to severe LVF with decompensation peripheral hypoperfusion (shock) AV conduction abnormalities (2nd/3rd degree heart block) SEVERE COPD/asthma...eh...maybe, if they have dyspnea upon admin cocaine use |
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5 relative CIs for BBs
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hx of asthmar
already using BB already using non DHP CCB severe PVD (can decrease perfusion) uncontrolled/brittle insulin dependent diabetes |
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ACEI- whom to give to (2)
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ACEI- everyone gets if NSTEMI- may be beneficial (guidelines) in all pt after MI
High risk NSTEMI/UA needs one |
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ACEI evidence(3)
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no placebo controlled trials in NSTE-ACS
20% RRR in combined endpoint of CV death, MI, stroke, cardiac arrest in HIGH RISK pt no benefit in low risk but how many low risk pt are you going to see with MI |
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ACEI absolutely should be given in what 3 pt pops (3)
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use in pt with diabetes
LVEF <40% (HF) hypertension |
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3 As of ABCDEs of treatment : think through when you would give each of these
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A: antiplatelet- asa, plavix, GP IIb/III a inhibitors
anticoagulation-UFH/LMWH ACEI/ARB |
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when NOT to give LMWH (2)
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24h prior to CABG
CrCl < 60 unless monitoring anti Xa |
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2 Bs of ABCDEs of treatmetn
goal BP |
Beta blockade
BP control (ACEI and BBs firstline)- (<130/85 or 80 if diabetes |
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2 Cs of ABCDEs
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cholesterol treatment (goal < 70 mg/dL) ALL should be on potent, HD statin
cig smoking cessation |
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2 Ds of ABCDEs
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diabetes managemnet (<7% A1C)
Diet |
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Exercise for NSTEMI/UA pt recommendation
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aerobic/weight bearing exercise 4-5 times per week for > 30 min
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aldosterone blockade- effect on all cause mortality
when to start? what type of pt? (2) |
aldosterone blockade- improved mortality in eplenerone/spironolactone if started 3-14 days post MI with ACEI/BB at optimal doses
pt had SYMPTOMATIC HF and EF <40% |
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UHHH GP inhibitors...when do you even give these
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---look up
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PT WITH STEMI- OH NO what do you do (2)
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MONA
beta blockade- oral within first 24 h- mortality benefit in both early and late phases of STEMI- treat fo lyfe |
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ok pt is on EMS after 911 call- what do you want them to do on the way to hospital? (2)
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encourage 12 lead ECG
consider prehospital fibrinolytic if capable and EMS to needle within 30 min (goal) |
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door to needle time goal
EMS to balloon time goal |
door to needle (ER door-->fibrinolytic) time goal- 30 min
EMS to balloon time goal- within 90 min of arriving at hospital (>95% efficacy at restoring flow)- if you can't do this (not at a good hospital) give the fibrinolytic |
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goal total ischemic time
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120 min
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when is primary PCI indicated (give PCI first)
meds given at this time? |
preferred if in hospitals with cath lab and surgical back up
abciximab rec'd ASAP before PCI |
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primary PCI preferred if...(4)
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high risk pt (cardio shock)
CI to fibrinolysis (ICH, bleeds) late presentation (>3h from sx onset- maybe person just sat there) dx of STEMI in doubt (like a really young person that is thin) |
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pt who recieve fibrinolysis- what do we need to do with them after?
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pt receiving fibrinolysis should be risk stratified to ID need for further revascularization with PCI or CABG
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in addition to PCI (primary or secondary) in STEMI, all pt should receive what? (2)
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all pt should receive late hospital care and secondary prevention of STEMI
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what is MoA of thrombolytis
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exogenous plasminogen activators -
plasmonigen is proenzyme converted to plasmin by plasminogen activators (which then digests fibrin) |
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thrombolytic administration timing for STEMI- max, preferable time, ideal time
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administer within 12h of symptom onset
prefer within 6 h IDEALLY within 30 min of arrival to hospital (door to needle) |
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3 non selective thrombolytics
what does non selective entail |
streptokinase
anistreplase urokinase nonselective means they bind CIRCULATING AND BOUND plasminogen (more bleeds) |
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3 selective thrombolytics
what does selective entail |
alteplase (tPA)
reteplase (rPA) tenecteplase more selective for bound plasminogen (already formed clots) |
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most selective thrombolytic
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tenecteplase
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STK 2 properties (2)
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STK antigenic- can occur when given SECOND time (challenge etc) so not really given anymore since it also has low efficacy
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Tenecteplase dosing frequency
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once
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alteplase (TPA) dosing
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IVP, then 0.75 mg/kg over 30 min, then 0.5 mg/kg over 60 min
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reteplase dosing
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IVP q30 min x2
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stent vs thrombolytics- mortality effect, other effects (4)
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stent > thrombolytics for mortality rate decreases
also smaller infarct size, less reinfarcation less medical cost, less CV event readmission for HF/ischemia |
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8 absolute CIs for thrombolytics
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-ANY prior hemorrhagic CVA
-ischemic CVA within 3 months?? Why? Transformation into hemorrhagic stroke intracranial neoplasma or AVM ( bulge in artery at risk of rupture) internal bleeds aortic dissection (more bleed risk) -facial/closed head trauma- increase risk of hemorrhage -same with diabetic retinopathy -malignant BP (>200/120)- also increases risk of brain hemorrhage |
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relative CIs for thrombolytics- look at list
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age >75
active peptic ulcer pregnancy (more abortions) Hx TIA/ischmemia GREATER than 3 months ago ANYTHING BLEED RELATED THAT ISN"T IN ABSOLUTE CI LIST |
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monitoring for efficacy after thrombolytic (2)
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monitor ST elevation (EKG)
monitor sx for 60-180 min after initiation of fibrinolytic |
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3 noninvasive findings that indicate reperfusion (after thrombolytic)
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relief of symptoms
maintenance and restoration of hemodynamic/electrical stability reduction of >=50% of initial ST segment elevation pattern on f/u ECG 60-90 min after initiation of therapy |
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after giving thrombolytic- 6 conditions where you could do rescue PCI/CABG
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cardiogenic shock
severe CHF/pulmonary edema ventricular arrhythmias hemodynamic/electrical instability persistent ischemic symptoms reduction of >=50% of initial ST segment elevation not achieved 60-90 min after giving drug |
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thrombolytic + GPIIb/IIIa inhibitor effects
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increases bleeds, not much diff in mortality (30 day)
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anticoag for STEMI- when to stop (2) in PCI vs. thrombolytics
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anticoag d/ced immediately after PCI/CABG
if combining with thrombolysis, use concurrently for >=48 h, until discharge preferably |
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3 anticoags for STEMI use
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IV UFH
enoxaparin fondaparinux (no bivalirudin) |
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7 things to monitor with anticoag in STEMI
3 for drug, 3 for efficacy, 1 for...idk |
troponin
aPTT with heparin H/H q6h platelets sx SCr telemetry (EKG) |
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age > 75 dosing for enoxaparin (2)
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no bolus (usually 30 mg IV-->then SQ)
reduce dose to 0.75 mg/kg SQ BID |
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contraindication for fondaparinux
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SCr > 3 mg/dL
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thienopyridine use in STEMI
not studied in what? how is dosing different, or is it the same? |
if stented, use plavix the same as you would in UA/NSTEMI regardless of if they got thrombolytic
no bolus primary PCI was exluded from study |
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duration of thienopyridine with ASA in STEMI (2)
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at least 14 days
reasonable up to 1 year |
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plavix and CABG
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hold >= 5 days before
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prasugel vs plavix in STEMI efficacy
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better outcomes with prasugel but more risk in bleeds
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prasugel- NOT studied in what STEMI population
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med managmenet (thrombolytic monotherapy)
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when to start ACEI in STEMI (2)
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start after SL nitro and BB
usually start within first 24 h for pt |
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patient pop that receives ACEI for STEMI (4)
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anterior STEMI if they have HF signs (congestion), LVEF <40%, and EVERYONE WITH STEMI UHH OK if their BP allows
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lifelong therapy with ACEI for STEMI pt if what? (3)
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lifelong therapy if pt has LV dysfunction, CHF, anterior MI
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2 relative contraindications for ACEI
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hypotension, chronic renal failure
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2 absolute CI for ACEI
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acute renal failure, bilateral RAS
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bad ACEI- why?
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enalaprilat (IV form- increase MORTALITY due to fast onset, makes ppl hypotensive)
avoid- increases mortality |
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lisinopril dosing for STEMI
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5-10 mg po qd
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ACEI dosing duration
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forever
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4 important monitoring things forr ACEs
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SBP > 90-100
renal fxn (<30 % increase from baseline) HF sx K+<=5 |
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5 ADR for ACEI
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cough
angioedema (can occur even if on med for long time) diarrhea taste alteration dizzy |
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aldosterone antagonist in STEMI
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same criteria as in NSTEMI
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goal LDL for STEMI pt (2 options)
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goal LDL < 100 mg/dL??? i thought it was 70 for the NSTEMI...check. option <70 if very high risk (has additional risk factor- diabetes, smoker, recurrent)
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AMI effect on LDL
what this means for measuring LDL in STEMI/NSTEMI pt |
AMI artificially depresses cholesterol by 1/3 to 1/2 so you MUST measure within 24h of presentation or else wait 6-12 weeks
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first 24 h of STEMI- what to do (7)
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1) asa within 1st 24 hr- chewed
2) fibrinolytic if not primary PCI 3) UFH/LMWH 4) plavix load 5) metoprolol 5 mg IV, then po 6) ACEI/ARB 7) check lipids- statin |
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7 things to do to pt after first 24h, during hospitalization for STEMI
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1) asa- maybe with plavix
2) UFH/LMWH (d/c once PCI/CABG is done, if it is done) 3) plavix 75 mg qd 4) titrate up orally until HR 55-60 5) titrate ACEI as tolerated to doses in clinical trials 6) keep on statin 7) consider aldosterone blocker if meets requirements |
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6 long term things to keep pt on for STEMI
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ASA (1-2 baby asa)
plavix BB ACEI maybe spirono statin |