+ All Categories
Home > Documents > Ppt chapter 37

Ppt chapter 37

Date post: 24-Apr-2015
Category:
Upload: stanbridge
View: 117 times
Download: 4 times
Share this document with a friend
Description:
 
51
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins Chapter 37 Drugs Affecting the Lower Gastrointestinal Tract
Transcript
Page 1: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Chapter 37

Drugs Affecting the Lower Gastrointestinal Tract

Chapter 37

Drugs Affecting the Lower Gastrointestinal Tract

Page 2: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Question Question

• In what part of the colon are the majority of fluids and electrolytes reabsorbed?

– A. Proximal colon

– B. Mid-segment of the colon

– C. Distal colon

– D. Rectum

Page 3: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

AnswerAnswer

• A. Proximal colon

• Rationale: Absorption of fluid and electrolytes occurs primarily in the proximal colon.

Page 4: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Physiology Physiology • The large intestine is approximately 5 feet long (1.5 m)

and 2.5 inches (6.5 cm) in diameter.

• The longitudinal muscle fibers on the outer surface of the large intestine are in three layers.

• The large intestine is composed of the cecum, colon, rectum, and anal canal.

• The contents from the small intestine enter the cecum through the ileocecal valve.

• Peristalsis moves the contents through the small and large intestines.

• Large amounts of mucus are secreted by goblet cells in the epithelial layer of the large intestine.

Page 5: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Large IntestinesLarge Intestines

Page 6: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Pathophysiology Pathophysiology

• Flatus is a normal by-product of digestion.

• Diarrhea is the frequent passage of loose or liquid stools.

• Constipation is infrequent or incomplete passage of hard stools resulting from a decrease in peristaltic activity.

• Irritable bowel syndrome (IBS) is a common disorder of the intestines characterized by altered bowel habits and pain.

• Inflammatory bowel disease (IBD) is a general term that includes both ulcerative colitis and Crohn disease.

Page 7: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Antiflatulents Antiflatulents

• Antiflatulents decrease gas production.

• Prototype drug: simethicone (Mylicon)

Page 8: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Simethicone: Core Drug Knowledge Simethicone: Core Drug Knowledge

• Pharmacotherapeutics

– Relieves the discomfort of excess gas

• Pharmacokinetics

– Not absorbed from GI tract. Excreted: feces.

• Pharmacodynamics

– Defoaming action that alters the surface tension of gas bubbles

Page 9: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Simethicone: Core Drug Knowledge (cont.)Simethicone: Core Drug Knowledge (cont.)

• Contraindications and precautions

– Simethicone has no contraindications or precautions.

• Adverse effects

– No substantial adverse reactions

• Drug interactions

– No drug interactions with simethicone are known.

Page 10: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Simethicone: Core Patient Variables Simethicone: Core Patient Variables

• Health status

– Assess bowel sounds and abdominal pai.

• Lifestyle, diet, and habits

– Assess dietary choices.

• Environment

– Assess the environment where the drug will be given.

Page 11: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Simethicone: Nursing Diagnoses and Outcomes Simethicone: Nursing Diagnoses and Outcomes

• Acute Pain related to the presence of flatus

– Desired outcome: Within 2 to 3 hours of using simethicone, the patient will experience a decrease in abdominal pain and distention.

Page 12: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Simethicone: Planning and InterventionsSimethicone: Planning and Interventions

• Maximizing therapeutic effects

– Simethicone should be given after meals and at bedtime to increase its effectiveness.

– The suspension form of the drug must be shaken to ensure that the active ingredients are well dispersed.

Page 13: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Simethicone: Teaching, Assessment, and EvaluationSimethicone: Teaching, Assessment, and Evaluation

• Patient and family education

– Teach patients to take simethicone after each meal and at bedtime.

– Caution patients not to increase the dosage.

• Ongoing assessment and evaluation

– Assess abdominal pain and distention periodically throughout simethicone therapy to monitor the effectiveness of the drug.

Page 14: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

QuestionQuestion

• Simethicone has the following contraindication(s)

– A. Cardiac disease

– B. Renal insufficiency

– C. No contraindications

– D. Both A and B

Page 15: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

AnswerAnswer

• C. No contraindications

• Rationale: Simethicone has no contraindications or precautions.

Page 16: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Antidiarrheals Antidiarrheals

• Antidiarrheals slow intestinal motility, allowing time for fluid reabsorption and better stool formation.

• Prototype drug: diphenoxylate HCl with atropine sulfate (Lomotil, Lonox)

Page 17: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Diphenoxylate: Core Drug Knowledge Diphenoxylate: Core Drug Knowledge

• Pharmacotherapeutics

– Adjunct in treating diarrhea

• Pharmacokinetics

– Administered: oral. Metabolism: liver. Excreted: urine and feces.

• Pharmacodynamics

– Acts on the smooth muscle of the intestine to slow intestinal motility and prolong intestinal transit time, allowing for the reabsorption of fluid.

Page 18: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Diphenoxylate: Core Drug Knowledge (cont.)Diphenoxylate: Core Drug Knowledge (cont.)

• Contraindications and precautions

– Hypersensitivity

• Adverse effects

– Drowsiness and dizziness

• Drug interactions

– MAOIs, alcohol, barbiturates, and tranquilizers

Page 19: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Diphenoxylate: Core Patient Variables Diphenoxylate: Core Patient Variables

• Health status

– Assess symptoms and contraindications to therapy.

• Life span and gender

– Pregnancy Category C drug

• Lifestyle, diet, and habits

– Assess history of substance abuse.

• Environment

– Assess the environment where the drug will be given.

• Culture and inherited traits

– Assess cultural beliefs regarding bowel habits.

Page 20: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Diphenoxylate: Nursing Diagnoses and Outcomes Diphenoxylate: Nursing Diagnoses and Outcomes

• Diarrhea related to the causative factor (if identified)

– Desired outcome: Diarrhea will be controlled through the use of diphenoxylate HCl with atropine sulfate.

• Risk for Injury related to drowsiness and dizziness secondary to drug therapy

– Desired outcome: The patient will not sustain injury from drug therapy.

Page 21: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Diphenoxylate: Planning and InterventionsDiphenoxylate: Planning and Interventions

• Maximizing therapeutic effects

– Administered as ordered

• Minimizing adverse effects

– Decrease the dosage when the number of stools decreases.

– Assess for and report signs of atropine sulfate toxicity.

Page 22: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Diphenoxylate: Teaching, Assessment, and EvaluationDiphenoxylate: Teaching, Assessment, and Evaluation

• Patient and family education

– Teach patients not to exceed the prescribed dosage.

– Instruct patients to notify the prescriber if diarrhea persists for more than 2 days.

• Ongoing assessment and evaluation

– It is important to assess skin turgor and mucous membranes for loss of moisture because these signs indicate dehydration.

Page 23: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

QuestionQuestion

• Signs of atropine toxicity includes which of the following?

– A. Dry mouth

– B. Hypothermia

– C. Tachycardia

– D. Urinary retention

– E. All of the above

Page 24: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

AnswerAnswer

• E. All of the above

• Rationale: Assess for and report signs of atropine sulfate toxicity (e.g., dry mouth, flushing, hypothermia, tachycardia, and urinary retention) because this condition requires immediate medical attention.

Page 25: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Laxatives Laxatives • Drugs used to treat constipation are referred to as

laxatives.

• Laxatives are drugs that act directly on the intestine to promote peristalsis and evacuation of the bowel.

• Laxatives are classified as saline, hyperosmotic, stimulant, and bulk forming.

• Saline laxatives

– Attract or retain water in the intestinal lumen, resulting in an increased intraluminal pressure that stimulates peristalsis.

• Prototype drug: magnesium hydroxide (Milk of Magnesia)

Page 26: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Magnesium Hydroxide: Core Drug Knowledge Magnesium Hydroxide: Core Drug Knowledge

• Pharmacotherapeutics

– Constipation and prepare the bowel for surgery

• Pharmacokinetics

– Local effect on GI tract. Duration: 2 to 6 hours.

• Pharmacodynamics

– Attracting and retaining water in the intestinal lumen

Page 27: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Magnesium Hydroxide: Core Drug Knowledge (cont.)Magnesium Hydroxide: Core Drug Knowledge (cont.)

• Contraindications and precautions

– Abdominal pain

• Adverse effects

– Overactive bowel and fluid and electrolyte imbalance

• Drug interactions

– May decrease or increase the effects of many drugs

Page 28: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Magnesium Hydroxide: Core Patient Variables Magnesium Hydroxide: Core Patient Variables • Health status

– Determine any history of renal insufficiency.

• Life span and gender

– Assess age before administration.

• Lifestyle, diet, and habits

– Determine normal fluid intake.

• Environment

– Assess the environment where the drug will be given.

• Culture and inherited traits

– Cultural variations about frequency of bowel movements

Page 29: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Magnesium Hydroxide: Nursing Diagnoses and Outcomes Magnesium Hydroxide: Nursing Diagnoses and Outcomes

• Constipation related to dietary factors, fluid restrictions, decreased peristalsis, lack of activity, changes in activity, postoperative state, GI disease or malfunction, or adverse effects from other drug therapy.

– Desired outcome: The patient will have a bowel movement after taking magnesium hydroxide.

Page 30: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Magnesium Hydroxide: Planning and InterventionsMagnesium Hydroxide: Planning and Interventions

• Maximizing therapeutic effects

– The patient should follow with a full glass of water to prevent dehydration and to promote a more rapid effect.

• Minimizing adverse effects

– Limit to short-term use.

– At least 2 hours should pass between administration of magnesium hydroxide and drugs that are known to interact with it.

Page 31: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Magnesium Hydroxide: Teaching, Assessment, and EvaluationMagnesium Hydroxide: Teaching, Assessment, and Evaluation

• Patient and family education

– Short-term use of medication

• Ongoing assessment and evaluation

– Assess color, consistency, and amount of stool produced to monitor effectiveness of magnesium hydroxide.

Page 32: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

QuestionQuestion

• Magnesium hydroxide is a laxative that can be used for long-term therapy.

– A. True

– B. False

Page 33: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

AnswerAnswer

• B. False

• Rationale: Magnesium hydroxide is not for long-term use. Fluid and electrolyte imbalance can occur with large doses given frequently.

Page 34: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Drugs Used to Treat Irritable Bowel Syndrome Drugs Used to Treat Irritable Bowel Syndrome

• Serotonin receptors in the bowel play a role in bowel motility.

• Drugs that work at these receptors can alter symptoms of IBS.

• Blockade of serotonin receptor subtype 3 (5-HT3) decreases the diarrhea associated with IBS.

• Prototype drug: alosetron (Lotronex)

Page 35: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Alosetron: Core Drug Knowledge Alosetron: Core Drug Knowledge

• Pharmacotherapeutics

– Treatment of IBS

• Pharmacokinetics

– Administered: oral. Metabolism: liver. Absorption: Excreted: urine and feces.

• Pharmacodynamics

– Blocks the 5-HT3 receptor

– Alters visceral sensation, decreasing abdominal discomfort and pain

Page 36: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Alosetron: Core Drug Knowledge (cont.)Alosetron: Core Drug Knowledge (cont.)

• Contraindications and precautions

– History of chronic constipation

• Adverse effects

– Constipation

• Drug interactions

– No important drug interactions with alosetron have been identified.

Page 37: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Alosetron: Core Patient Variables Alosetron: Core Patient Variables

• Health status

– Assess type of IBS.

• Life span and gender

– Pregnancy Category B drug

Page 38: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Alosetron: Nursing Diagnoses and Outcomes Alosetron: Nursing Diagnoses and Outcomes

• Risk for Altered Elimination, Constipation, related to potential adverse effects of alosetron

– Desired outcome: The patient will not develop serious constipation while on alosetron.

Page 39: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Alosetron: Planning and InterventionsAlosetron: Planning and Interventions

• Maximizing therapeutic effects

– No specific actions are recommended.

• Minimizing adverse effects

– Confirm that the patient has received the Medication Guide from the prescriber before starting therapy and has read it and understands it.

– Answer questions about therapy.

Page 40: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Alosetron: Teaching, Assessment, and EvaluationAlosetron: Teaching, Assessment, and Evaluation

• Patient and family education

– Educate patients about the potential adverse effects.

– Instruct patients to report any constipation or signs of ischemic colitis.

• Ongoing assessment and evaluation

– Assess the patient throughout alosetron therapy for constipation.

Page 41: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

QuestionQuestion

• What is the major adverse effect of alosetron?

– A. Diarrhea

– B. Constipation

– C. Tachycardia

– D. Nephrotoxicity

Page 42: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

AnswerAnswer

• B. Constipation

• Rationale: Alosetron’s major adverse effect is constipation.

Page 43: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Drugs Used to Treat Inflammatory Bowel Disease Drugs Used to Treat Inflammatory Bowel Disease

• Drug therapy cannot cure IBD.

• The drug groups used to treat IBD include the 5-aminosalicylic acid (5-ASA) preparations, corticosteroids, and drugs that suppress the immune system.

• 5-ASA preparations

– Aminosalicylates (5-ASA) are the anti-inflammatory drugs most commonly prescribed for IBD.

• Prototype drug: mesalamine (Asacol, Pentasa, Lialda)

Page 44: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Mesalamine: Core Drug Knowledge Mesalamine: Core Drug Knowledge

• Pharmacotherapeutics

– Ulcerative colitis and proctosigmoiditis

• Pharmacokinetics

– Formulation: tablet, capsule, suppository, and rectal suspension. Metabolism: liver. Excreted: feces.

• Pharmacodynamics

– The action of mesalamine is unknown.

Page 45: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Mesalamine: Core Drug Knowledge (cont.)Mesalamine: Core Drug Knowledge (cont.)

• Contraindications and precautions

– Hypersensitivity

• Adverse effects

– Diarrhea, abdominal pain, cramps, flatulence, nausea, and headache

• Drug interactions

– Azathioprine, mercaptopurine, and salicylates

Page 46: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Mesalamine: Core Patient Variables Mesalamine: Core Patient Variables

• Health status

– Assess for hypersensitivity.

• Life span and gender

– Pregnancy Category B drug

Page 47: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Mesalamine: Nursing Diagnoses and Outcomes Mesalamine: Nursing Diagnoses and Outcomes

• Risk for Altered Elimination, Constipation, related to potential adverse effects of mesalamine

– Desired outcome: The patient will not develop serious constipation while on mesalamine.

• Acute pain related to drug-induced adverse GI effects

– Desired outcome: The patient will take acetaminophen for pain as needed.

Page 48: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Mesalamine: Planning and InterventionsMesalamine: Planning and Interventions

• Maximizing therapeutic effects

– Before administering the enema, shake the bottle thoroughly.

• Minimizing adverse effects

– Administer the oral medication at even intervals throughout the day.

Page 49: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Mesalamine: Teaching, Assessment, and EvaluationMesalamine: Teaching, Assessment, and Evaluation

• Patient and family education

– Educate the patient about the potential adverse effects.

– Instruct the patient how to administer an enema if ordered.

• Ongoing assessment and evaluation

– Assess the patient throughout mesalamine therapy for relief of pain.

Page 50: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

QuestionQuestion

• Mesalamine may be prescribed for all age groups.

– A. True

– B. False

Page 51: Ppt chapter 37

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

AnswerAnswer

• B. False

• Rationale: Mesalamine is not approved for use in children.


Recommended