Wk2 Flashcards
Pharmacokinetic properties (LADME)
Liberation: disintegration, dispersal, dissolution
Absorption: how’s it absorbed
Distribution: how does it spread through the body
Metabolism: is it turned chemically inside the body
Excretion: how is it eliminated form the body
Describe administration of medication the systemic effect
Most drugs given orally
Some changed by GI tract
Drugs absorbed by GIT pass through portal system to liver
Only once passed through liver can drug be distributed in systemic circulation
All this is known as oral bioavailability - titrating drugs bc differs form pt to pt
What are pharmacodynamics
The biochemical and physiological effects of drugs in the body Drug response Drug concentration vs effect Cellular response Modify cell function Competitive (reversed) No competitive (can't be reversed)
Information about the GI tract
Major endocrine systems of the body
Acid secreted by parietal cells
Maintains stomach acid at pH 1-4
Acid secretion stimulated by large, dfatty meals, excessive amounts of alcohol, emotional stress
What is the enteric nervous system
2 major nerve plexuses in wall of GIT
Sub mucosal and Myenteric
Meds to control gastric secretion
Antacids, histamine H2, proton pump
Meds to control motility
Purgatives, antidiarrhoeals, antispasmodics
Meds to control vomiting
Emetic, antiemetic
What are antacids
Don’t prevent overproduction of acid , neutralise acid once it’s in the stomach
Weak bases
Combine with HCL to raise pH
PH more than 4 = inactive pepsin (digestive protease enzyme released by chief cells that function to degrade food protein into peptides)
Types of antacids
Aluminium salts: constipation effects
Sodium bicarbonate: highly soluble, quick onset, short duration, issues with heart failure, renal issues, hypertension
Magnesium salts: laxative effects, dangerous in renal failure (accumulation of MG)
Calcium salts: may cause constipation
Siemthicone: reduce bloating, decrease surface tension of gas bubbles causing them to combine
Nursing considerations in use of antacids
May inactivate other drugs
Alteration of pH causes reduced drug absorption
Administer other drugs 2 hrs before or after
What is pharmacokinetics
Explores what the body does to the drug Mechanisms of absorption/distribution Rate of onset Action of drug Duration Effects Route of excretion
What are H2 antagonists
Histamine is a potent stimulant agent for acid production in the stomach
Acid secretion increased by H2 -receptor activation.
H2 Antagonists block the actions of histamine & reduce acid production
Reduce acid secretion
what are the side effect and nursing considerations of H2 antagonists
- Diarrhoea, constipation, headaches, dizziness
- Rarely hypotension, liver problems, clotting disorders
- Can interact with other drugs & reduce absorption
- Assess for allergies and impaired renal or liver function.
- Take 1 hour before or after antacids
- Ranitidine may be given intravenously; follow administration guidelinesH2 antagonists may be administered with or without food
- Assess effectiveness of medications relief from sysmptoms
Examples of H2 antagonists
Zantac (Ranitidine)
Tazac (Nizatidine)
Tagamet (Cimetidine)
Pepcid (Famotidine)
Gastric ulcer: 20% = H2 antagonist
Duodenal ulcer: 80% = H2 antagonist with or without h.pylori