FINALS TDM/ cardiotropics Flashcards

1
Q

Involves the analysis and evaluation of circulating concentrations of drugs in blood

A

TDM/ Therapeutic Drug Monitoring

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

To ensure that a given drug dosage produces maximal therapeutic benefit and minimal toxic adverse effects

A

TDM/ Therapeutic Drug Monitoring

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Indications of TDM

A

1.Consequences of over- and under-dosing are serious
2. Narrow margin of safety
3. Good correlation between circulating concentrations and therapeutic or toxic effects
4. Change in patient’s condition that may affect circulating drug concentrations
5. Occurrence of drug interactions
6. Monitoring patient compliance

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

The rate at which the drug is absorbed is dependent upon the route of administration

Tablets & capsules require dissolution; liquids are rapidly absorbed

Transport mechanism: passive diffusion

Weak acids are absorbed in the stomach; weak bases in the intestine

A

Absorption

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

FACTORS AFFECTING ABSORPTION

A

CPIP

Changes in intestinal movement
pH
Inflammation
Presence of food or other drugs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Single most important factor

A

Timing

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Peak concentrations

A

1 hour after an orally administered dose

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

SAMPLE COLLECTION

A

Serum or heparinized plasma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Used to treat congestive heart failure and cardiac arrhythmias

Act on the conduction system of cardiac muscle

Net effect : slow down electrical conduction

A

CARDIOTROPICS

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Rapid sodium channel blockers

A

Class I

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Quinidine

A

Class I

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Procainamide

A

Class I

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Lidocaine

A

Class I

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Phenytoin

A

Class I

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Beta adrenergic blockers

Propranolol

A

Class II

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Potassium channel blockers

Amiodarone

A

Class III

17
Q

Calcium channel blockers

Verapamil

A

Class IV

18
Q

Digoxin and Digitoxin

A

DIGITAL GLYCOSIDES

19
Q

Inhibits membrane Na+-K+-ATPase
Decreases K+ and Mg+ and increases Ca+
Rapid onset of action : 1-2 h after oral administration

A

Digoxin

20
Q

Slower onset of action (1-4 hours oral)
Active metabolite : digoxin

A

Digitoxin

21
Q

Local anesthetic

Acute control and prevention of ventricular arrhythmias after myocardial infarction

Toxicity : convulsions, coma, respiratory depression, bradycardia, hypotension

A

Lidocaine

22
Q

For supraventricular and ventricular arrhythmias

Common formulation: quinidine SO4 & quinidine gluconate

Toxicity : cinchonism: vertigo, tinnitus, headache, visual disturbances and disorientation

A

Quinidine

23
Q

Supraventricular or ventricular arrhythmias

Metabolite : n-acetylprocainamide

Toxicity : reversible lupus-like syndrome w/ elevated ANA titers, urticaria, rash, agranulocytosis and nephrotic syndrome

A

Procainamide

24
Q

Antagonizes effects of epinephrine on the heart, arteries and arterioles of skeletal muscles and on the bronchus

Vasodilator: angina pectoris, hypertension

A

Propanolol

25
Q

For life threatening ventricular arrhythmias

A

Amiodarone

26
Q

For angina, hypertension and supraventricular arrhythmias

A

Verapamil