Medication for GI Flashcards

1
Q

Histamine 2

PUD

treatment of H.pylori

A

Drug:
* Histamine 2- receptor antagonists
* Cimetidine (H1 and H2)
* Ranitidine (H2)
* Famotidine

Therapeutic use
* treats gastric and duodenal ulcers
* GERD
* Zollinger Ellison syndrome, hypersecretion of gastric acid and development of acid and development of peptic ulcers
* Heartburn acid indigestion and sour stomach

MOA
* promotes ulcer healing by suppressing secretions of gastric acid
* prevents erosion of the gut wall
* Activation of H1 receptors produce symptoms of allergies
* Activation of H2 receptors are located on peripheral cells of the stomach and promote secretion of gastric actid

Side effects
Cimetidine:
* Antiandrogenic effect- binds two androgen receptors causing gynecomastia, reduced libido, and impotence

  • CNS effects- most likely in older adults who have renal or hepatic impairment
  • Confusion, hallucinations, CNS depression (lethargy, somnolence), and CNS excitation (restlessness, seizures)
  • Pneumonia- related to gastric pH elevation and decreasing healthy upper GI flora

Ranitidine & Famotidine:
* CNS effects are rare due to penetrating the BBB poorly

  • Does not cause anti androgenic effects
  • Pneumonia- related to gastric pH elevation

Drug interactions:
Cimetidine:
* Increases blood levels of Coumadin, Dilantin and theophylline
* Ranitidine & Famotidin

Pt. teaching
Cimetidine:
* Do not give cimetidine to the elderly due to CNS effects

Ranitidine:
* Immediate removal from shelves in 2020 due to cancer causing contaminants can build up over time

All:
* Educate and monitor for s/s of pneumonia or URI

Nurse education for PUD:

  • Small frequent meals for peptic ulcers
  • Stop smoking to prevent vasoconstriction
  • Decrease or stop NSAIDs
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2
Q

Proton pump inhibitors

A

Drugs
* Esomeprazole
* Lansoprazole
* Omeprazole

Therapeutic use
* GERD
* Gastric and duodenal ulcers

MOA
* blocks all acid production
* inhibits gastric acid pump of the parietal cells

Adverse effects
* HA,N,V,D
* Fractures (reduces acid secretion and decreases absorption of calcium)

  • Pneumonia (alter upper GI flora/reduces gastric acidity, impairment of WBC function)
  • Acid rebound (hypersecretion of gastric acid)
  • Intestinal infection with C. diff (diarrhea/abdominal pain)
  • Hypomagnesium (reduce intestinal magnesium absorption)
  • Gastric cancer (hypersecretion of gastrin)

Drug interaction
* Clopidogrel (decrease adverse effects and reduce beneficial effects)

  • Decrease absorption of HIV/AIDS medications

pt. education
* Most effective inhibitor of gastric secretions
* Short half-life
* More expensive
* Used for short term therapy and lowest dose possible
* Report serious adverse event symptoms ASAP

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3
Q

antacids

A

Drugs
* Aluminum hydroxide
* calcium carbonate
* magnesium hydroxide

Therapeutic use
* Heartburn
* GERD
* PUD

MOA

  • Neutralizes gastric acid by buffering hydrochloric acid
  • making hydrochloric acid less corrosive

Adverse effects
* Constipation (aluminum and calcium)

  • Diarrhea (magnesium)
  • Toxic levels of calcium and magnesium can accumulate in patients with renal failure (due to difficulty excreting medication from body)
  • May cause sodium loading due to large amounts of sodium in the antacid
  • Can exacerbate hypertension and heart failure

Drug interactions:
* Can influence the dissolution and absorption a H2RAs due to raising gastric pH

  • Can disrupt the absorption of iron and antibiotics

pt. education
* Use cautiously in renal failure due to difficulty excreting medication from body (calcium, magnesium)

  • Administer drug at least 1-2 hours from sucralfate, H2RAs, antibiotics and Iron
  • Do not use antacids for more than two weeks
  • Use cautiously in patients with hypertension, CHF, and renal insufficiency
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4
Q

sucralfate

A

Therapeutic use
* acute therapy and maintenace therapy of duodenal ulcers
* PUD

MOA
* ANTI-ulcer med
* promotes ulcer healing by creating a barrier against acid pepsin
* has no acid neturalizing capacity and does not decrease acid secretion
* not systemically absorbed

Adverse effects
* limited
* constipatation and nasuea most common

Drug interaction
* antacids may interfere with sucralfate effects
* may decrease the absorption of Phenytoin, theophylline, digoxin, warfarin, and fluroroquinolone antibiotics

pt education
* administer antacids and sucralfate atleast 1-2 hours a part
* Administer other medications and sucralfate at least 2 hours apart
* Administer 30 minutes to one hour prior to meals

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5
Q

Misoprostol

A

Therapeutic use
* prevents gastric ulcers caused by long term therapy with insets
* used to promote cervical ripening and in combination with mifepristone to induce medical termination of pregnancy

MOA
* Prostaglandin E1 analog: replacement for endogenous prostaglandis)
* prostaglandis helps protect the stomach by suppressing secretion of gastric acid, which promotes the secretion of bicarbonate and cytoprotective mucus
* asprin and other incidents cause gastric ulcers by inhibiting prostaglandin biosynthesis

Adverse effects
* Diarrhea, and abdominal pain
* spotting and dysmenorrehea in women

contraindicated in pregnant women

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6
Q

Bulk forming laxatives

A

drugs
* Psyllium

Therapeutic use
* constipation
* therapeutic group 3

MOA
* contains natural or semisynthetic polysaccarides and cellulose derived from grains and other plant material
* fxn like fiber
* causes water to be retained in stool
* agents are non-digestable and non-absorbable

Adverse effects
* Esophageal obstruction
* gas formation
* intestinal obstruction
* may be contraindicted in pt. who may have GI obstruction or impaction

pt. education
* glass of water to prevent esophageal obstruction

  • Should produce a soft formed stool in 24-72 hours
  • Do not use in patients who may have GI obstructions or impaction & monitor for S/S of intestinal obstruction when given to patients
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7
Q

laxitive education

A
  • Increase fluids and fiber
  • Dietary fiber is always best before chemical use
  • Have a bowel movement when the need is felt (defecation reflex)
  • Exercise after meals
  • Laxative overuse can lead to electrolyte imbalance
  • Do not use in patients who may have GI obstructions or impaction & monitor for S/S of intestinal obstruction when given to patients
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8
Q

Surfactant laxatives

A

Drug
* Docusate sodium

Theapeutic use
* constipation
* Therapeutic group 3

MOA
* Lower surface tension which faciliates the penetration of water into the feces
* acts onto the intestinal wall to inhibit fluid absorption and stimulate secretion of water and elctrolyes into the intestinal lumen

** Adverse effects**
* abdominal cramping

pt education
* should produce a soft stool with 1-3 days
* best for cardiac patients

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9
Q

stimulate laxatives

A

Drug
* Bisacodyl
* rectal suppository & PO enteric tablet
* Senna

Therapeutic use
* constipation
* treatment of opiod induced constipation
* Therapeutic group II

MOA
* Stimulates intestinal motility (nerve stimulation)
* increases the amount of water and electrolytes within the intestinal lumen by increasing secretion of water into the intestine
* Reduced water and electrolyte absorption

Adverse Effects
* systemic absorption followed by renal secretion may cause a harmless yellowish brown or pink color in the urine

Drug/ food interaction
* do not administer with milk and antacids
* accelerates dissolutions of the enteric coating

pt. education
* PO acts within 6-12 hours
* suppositorys act rapidly within 15-60 min
* produce a soft or semi fluid stool
* swallow pills intact due to enteric coating
– prevents gastric irritation
* seperate milk and antacids within 1-3 hours of ingestion
* urine discoloration is a harmless side effect

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10
Q

osmotic laxitives

A

Drug
* Magnesium hydroxide
* sodium phosphate
* magnesium citrate

Therapeutic use
* constipation
* bowel prep

MOA
* Draws water into the intestinal lumen
* peristalsis is stimulated by the swelling of the fecal mass due to the acculumation of water

Adverse effects
* can cause substantial loss of water which leads to electolytes imbalance
* magnesium can accumulate to toxic levels in those with renal issues
* sodium absorption can cause fluid retention
* sodium phosphate can cause acute renal failure in high-risk patients
* kidney disease
* ACE, ARBs, diruetics

pt education
* produce a soft or semi fluid stool within 6-12 hours of absorption
* rapid acting within 2-6 hours cause fluid evacuation in high doses
* high dose therapy is used for procedures
* pt. should increase fluid intake to avoid dehydration
* magnesium salts are contradicted in pt with kidney disease
* sodium phsophate should be avoided din high-risk pt
* MOM in the Am for a bowel mvmt in the Pm

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11
Q

Lubricants

A

Drugs
* Glycerin suppository
* mineral oil

Therapeutic use
* constipation

MOA
* lubricates intestinal wall and softens stool

Adverse effects
* affects absorption of fat soluble vitamins

produces stool within 12-18 hours

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12
Q

Loperamide

A

Therapeutic use
* Dirrhea
* reduce the volume of discharge from ileostomies

MOA
* a strucutal analogue of meperidine
* suppresses bowel motility
* suppresses fluid secretion into the intestinal lumen

Adverse effects
* constipation

benefits over diphenoxylate
* blood is poorly absorbed and is not readily crossed the blood brain barrier
* very large oral doses do not elicit morphone like subjective effects
* Loperamine has little or no potential for abuse and is not regulated unter teh controlled substance act

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13
Q

Diphenoxylate with Atropine

A

Therapeutic use
* opioid used only for diarrhea
* in combination with atropine to discourage diphenoxylate abuse

MOA
* Acts through the autonomic nervous system on the nerve endings in the intenstinal wall
* reduces peristalis and GI motility
* Atropine–> anticholinergic agent
* decreases peristalis and muscular tone of the intestines

Adverse effects
* Constipation
* decreased respiratory effort if takin in high doses

Benefits
* drug is insoluable in water and cannot be abused by parental routes
* PO in antidiarrheal doses has no effect on the central neverous system

  • hold if patient is having symtoms of constipation
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14
Q

Ondansetron

A

Therapeutic use
* chemo related N/V/
* morning sickness of pregnancy

MOA
* serotonin receptor antagonist
* blocks type 3 serotonin receptors located in the CTZ and on the afferent vagal neutons in the upper GI tract

Adverse effects
* HA, diarrhea, constipation, dizziness and sedation
* prolongs the QT interval and poses a risk of torsades de point dysthythmia

Contraindications
* pt with electrolyte abnormalites
* heart failure
* brady dyrhythmias
* long QT syndrome
* those taking other QT drugs

Benefits
* does not block dopamine receptors
* does not cause the extrapyramidals effect scene with anti-emetic phenothiazines

pt. nurse
* education on most common side effect
* not to be used for long term use

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15
Q

Dexamethasome

A

Therapeutic uses
* Chemo related N/V/
* Used in combination with other antiemetics IV

MOA
* suppression on emesis is unknown

Adverse effects
* uses intermittent in short term therefore serious side effects are absent

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16
Q

Lorazepam

A

Therapeutic effects
* CINV

MOA
* benzodiazepine
* GABA antagonist
* producing a calming effect

adverse effects
* potential for abuse/ overdose

benefits
* sedation
* suppression of anticipatory emesis
* production of amnesia

Pt. teaching
* depression from lorazepam use
* educate on the risk of abuse and overdose

17
Q

promethazine

A

Therapeutic use
* N/V associated with surgery, cancer therapy and toxins
* CINV

MOA
* A phenothiazine (dopamine antagonist(
* suppresses vomitting by blocking dopamine-2 receptors in the chemoreceptor trigger zone

Adverse effects
* respiratory depression
* sedation
* EPR
* anti-cholinergic effects
* hypotension
* local tissue injury

Contraindication
* patients under 2

pt education
* NEver give IV or SQ
* NEVER GIVE TO CHILDREN UNDER 2
* educate on the risk of sedation and respiratory depression from promethazine use
* anticholinergic effects (decreased everythhing except for hr )
* dystonia, akathisia, parkinsim characteristics

18
Q

Metoclopramide

A

MOA
* suppresses emesis by blocking dopamine and seratonin receptors
* increases upper GI motility
* increases lower esophageal spincter pressure and peristalsis

Therapeutic use
* Oral Metoclopramide
– Diabetic gastroparesis
– Suppression of gastroesophageal reflux
* IV Metoclopramide
– Suppression of post-op nausea and vomiting
– Suppression of CINV
– Facilitation of small bowel intubation
– Facilitation of radiologic examination of the GI tract

Adverse effects
* High dose therapy:
* Sedation, diarrhea, insomnia

  • Long term high dose therapy:
  • Irreversible tardive dyskinesia (Repetitive, involuntary movements of the arms, legs, and facial muscles)
  • Drug interactions: Limited

Contraindications:
* Patients with GI obstruction, perforation, or hemorrhage

  • Associated with an excess risk of congenital malformations when used during the first

pt. education
* To decrease risk of tardive dyskinesia treatment should be as brief as possible using the using the lowest effective dose

  • Do not give during the first trimester of pregnancy