Elm 12 Stable Angina Flashcards
Q: What is the main cause of chest pain in both angina and acute coronary syndrome (ACS)?
A: Cardiac ischemia.
Q: How does stable angina differ from ACS in terms of pain resolution?
A: Stable angina resolves with rest after a few minutes, while ACS does not resolve quickly or with rest.
Q: List the types of acute coronary syndrome from most to least harmful.
A: Unstable angina, non-ST elevated myocardial infarction (NSTEMI), ST elevated myocardial infarction.
Q: What causes the chest pain associated with angina pectoris?
A: Cardiac ischemia leads to the release of pain mediators like protons, potassium, and adenosine, which signal to the CNS.
Q: Why is chest pain from the heart often interpreted vaguely by the body?
A: Because pain from the heart is unusual, the body interprets it vaguely, causing general chest pain.
Q: What are the four types of angina?
A: Stable angina, unstable angina, Prinzmetal’s angina, microvascular angina.
Q: What triggers stable angina, and how can it be relieved?
A: Triggers include exercise, excitement, and cold weather. It can be relieved by rest.
Q: What causes unstable angina, and why is it more serious?
A: Caused by atherosclerosis and a blood clot. It is more serious because it is unpredictable, cannot be relieved by rest, and may progress to myocardial infarction.
Q: How can angina be treated?
A: By reducing oxygen demand or increasing oxygen supply to the heart.
Q: What is the initial treatment recommended by NICE for angina?
A: Aspirin to prevent platelet aggregation and statins to lower LDL and prevent plaque worsening.
Q: Name some drugs used to treat angina.
A: Organic nitrates, beta blockers, calcium channel blockers, potassium channel activators.
Q: What is first pass metabolism?
A: It is when a drug is absorbed by the gut into the hepatic portal vein and taken to the liver, where much of it is detoxified, reducing the bioavailability of the drug.
Q: Why can’t drugs susceptible to first pass metabolism be taken orally?
A: Because they lose a significant amount of their effectiveness when processed by the liver.
Q: What are alternative routes of administration for drugs susceptible to first pass metabolism?
A: Topical/transdermal application, parenteral routes (injection), and mucus membrane routes (mouth sprays, vaginal, under the tongue).
Q: What was glyceryl trinitrate (GTN) originally used for?
A: It was used to make explosives.
Q: Who discovered the vasodilatory action of nitroglycerine?
A: Sobrero discovered it when he experienced headaches from handling nitroglycerine.
Q: Who first used amyl nitrite to treat angina, prompting the use of nitroglycerine for the same purpose?
A: Brunton used amyl nitrite to treat angina, prompting Murrell to use nitroglycerine.
Q: Why is the name GTN used instead of nitroglycerine?
A: Because of its high association with explosives.
Q: In what forms can GTN be administered to relieve acute angina?
A: GTN can be administered sublingually (injection), buccally (mouth spray), or as a patch.
Q: How long do the effects of GTN last for relieving acute angina?
A: The effects last for 20-30 minutes.
Q: What is a key characteristic of organic nitrates like GTN in terms of their activation?
A: They are prodrugs that need to be metabolized at the site of action (vasculature or heart).
Q: What is the active form of organic nitrates, and how is it produced?
A: The active form is nitric oxide (NO), produced through metabolism.