IHD Part III (ACS) Flashcards
what are the three subtypes of ACS
- unstable angina
- STEMI
- NSTEMI
this subtype of ACS is a fully occlusive clot that may result in significant myocardial damage and release of biochemical markers
STEMI
this subtype of ACS is usually a transient partially occlusive clot that does not result in myocardial cellular damage or release of biochemical markers
unstable angina
this subtype of ACS is similar to unstable angina as it is a transient partially occlusive clot; however myocardial cellular damage occurs and there is an increase in biochemical markers
NSTEMI
how is ACS diagnosed
- patient sx’s
- ECG findings
- Lab results
true or false: ischemic chest pain present in ACS is relieved by SL NTG
false!!!
these are biochemical markers that are released into the blood on myocardial cell death. they are sensitive and specific for myocardial necrosis
troponin and CK MB
what are some complications of ACS (more so STEMI then NSTEMI)
- arrhymias/sudden cardiac death
- HF
- angina
- HTN
- cariogenic shock
- embolic stroke
- re-infarction
what is the main goal of ACUTE management of STEMI
reperfusion: opening the infarct related artery
KE presents with chest pain (not relieved by SL NTG), N/V, diaphoresis. PMHx is significant for stable CAD. current BP is 92/56 mmHg and HR is 10bpm. which of these medications should be given to KE immediately?
a) ASA EC 325mg orally x 1 dose
b) ASA 81mg two tabs chewed x 1 dose
c) NTG IV drip at 20mcg/min
d) metoprolol 5mg IV x 1 dose
B - Aspirin 81mg two tabs chewed x 1 dose
this repercussion strategy is preferred as it reduces death, MI, stroke, and major bleeding compared to the other strategy
PCI - PCI vs thrombolysis will entirely depend on the institution + resources
these agents are plasminogen activators: they convert plasminogen to plasmin which results in clot lysis. e.g. Alteplase, Reteplase and Tenecteplase
average time to repercussion (restore blood flow) is 45-60 mins
thrombolytics
who should NOT receive thrombolytics?
Absolute Contraindications:
- any prior hemorrhagic stroke
- ischemic stroke within 3 months (except in past 4.5 hours)
- intracranial neoplasm or arteriovenous malformation
- active internal bleeding
- aortic dissection
- considerable facial trauma or closed head trauma in the past 3 months
- intracranial or intraspinal surgery within 2 months
- severe, uncontrolled HTN (unresponsive to emergency therapy)
Relative Contraindications:
- BP > 180/110 mmHg on presentation or history of chronic poorly controlled hTN
- history of ischemic stroke greater than 3 months before
- recent major surgery (less than 3 weeks before)
- traumatic or prolonger CPR (> 10 mins)
- recent internal bleeding (within 2-4 weeks)
- active peptic ulcer
- noncomressible vascular punctures
- pregnancy
- known intracranial pathology (dementia)
- OAC
what is the main adverse effect of thrombolytics
bleeding - including hemorrhagic stroke!!!
who is at an increased risk of intracranial hemorrhage with fibrinolysis?
- older age
- females
- low body weight ( <70 kg female and < 80 kg for male)
- prior stroke
- HTN ( BP > 160 - 170/95 mmHg, at any time)
what needs to be monitored when a patient is on thrombolytic therapy
- bleeding
- mental status changes for signs of intracranial hemorrhage
- baseline aPTT, INR, CBC (for Hgb and platelets)
this type of antiplatelet therapy is an irreversible inhibitor of COS therefore inhibits platelet aggregation. For STEMI, loading dose here is 162 - 325 mg (chewed) x 1 dose and maintenance dose is 81 mg/day
ASA
what are some adverse effects of ASA
GI: N/V, heartburn, epigastric pain, ulceration
bleeding
hypersensitivity rash (Rare)