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Chapter 37 
Drugs Affecting the Lower 
Gastrointestinal Tract 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
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
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
Answer 
• A. Proximal colon 
• Rationale: Absorption of fluid and electrolytes occurs 
primarily in the proximal colon.
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. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Large Intestines 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
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. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Antiflatulents 
• Antiflatulents decrease gas production. 
• Prototype drug: simethicone (Mylicon) 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
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 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
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. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
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. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
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. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Simethicone: 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. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Simethicone: 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. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
Question 
• Simethicone has the following contraindication(s) 
– A. Cardiac disease 
– B. Renal insufficiency 
– C. No contraindications 
– D. Both A and B
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
Answer 
• C. No contraindications 
• Rationale: Simethicone has no contraindications or 
precautions.
Antidiarrheals 
• Antidiarrheals slow intestinal motility, allowing time for 
fluid reabsorption and better stool formation. 
• Prototype drug: diphenoxylate HCl with atropine sulfate 
(Lomotil, Lonox) 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
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. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Diphenoxylate: Core Drug Knowledge 
(cont.) 
• Contraindications and precautions 
– Hypersensitivity 
• Adverse effects 
– Drowsiness and dizziness 
• Drug interactions 
– MAOIs, alcohol, barbiturates, and tranquilizers 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
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. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
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. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Diphenoxylate: 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 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
toxicity.
Diphenoxylate: 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. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
Question 
• Signs of atropine toxicity includes which of the following? 
– A. Dry mouth 
– B. Hypothermia 
– C. Tachycardia 
– D. Urinary retention 
– E. All of the above
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
Answer 
• 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.
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) 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
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 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
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 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
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. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
• Environment 
– Assess the environment where the drug will be given. 
• Culture and inherited traits 
– Cultural variations about frequency of bowel 
movements
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. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Magnesium 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. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Magnesium 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. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
Question 
• Magnesium hydroxide is a laxative that can be used for 
long-term therapy. 
– A. True 
– B. False
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
Answer 
• B. False 
• Rationale: Magnesium hydroxide is not for long-term use. 
Fluid and electrolyte imbalance can occur with large 
doses given frequently.
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) 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
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 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
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. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Alosetron: Core Patient Variables 
• Health status 
– Assess type of IBS. 
• Life span and gender 
– Pregnancy Category B drug 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
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. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Alosetron: 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. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Alosetron: 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. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
Question 
• What is the major adverse effect of alosetron? 
– A. Diarrhea 
– B. Constipation 
– C. Tachycardia 
– D. Nephrotoxicity
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
Answer 
• B. Constipation 
• Rationale: Alosetron’s major adverse effect is 
constipation.
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) 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
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. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
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 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Mesalamine: Core Patient Variables 
• Health status 
– Assess for hypersensitivity. 
• Life span and gender 
– Pregnancy Category B drug 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
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. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Mesalamine: 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. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Mesalamine: Teaching, Assessment, and 
Evaluation 
• Patient and family education 
– Educate the patient about the potential adverse 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
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.
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
Question 
• Mesalamine may be prescribed for all age groups. 
– A. True 
– B. False
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
Answer 
• B. False 
• Rationale: Mesalamine is not approved for use in 
children.

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Ppt chapter 37

  • 1. Chapter 37 Drugs Affecting the Lower Gastrointestinal Tract Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 2. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 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
  • 3. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins Answer • A. Proximal colon • Rationale: Absorption of fluid and electrolytes occurs primarily in the proximal colon.
  • 4. 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. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 5. Large Intestines Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 6. 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. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 7. Antiflatulents • Antiflatulents decrease gas production. • Prototype drug: simethicone (Mylicon) Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 8. 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 Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 9. 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. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 10. 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. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 11. 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. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 12. Simethicone: 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. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 13. Simethicone: 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. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 14. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins Question • Simethicone has the following contraindication(s) – A. Cardiac disease – B. Renal insufficiency – C. No contraindications – D. Both A and B
  • 15. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins Answer • C. No contraindications • Rationale: Simethicone has no contraindications or precautions.
  • 16. Antidiarrheals • Antidiarrheals slow intestinal motility, allowing time for fluid reabsorption and better stool formation. • Prototype drug: diphenoxylate HCl with atropine sulfate (Lomotil, Lonox) Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 17. 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. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 18. Diphenoxylate: Core Drug Knowledge (cont.) • Contraindications and precautions – Hypersensitivity • Adverse effects – Drowsiness and dizziness • Drug interactions – MAOIs, alcohol, barbiturates, and tranquilizers Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 19. 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. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 20. 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. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 21. Diphenoxylate: 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 Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins toxicity.
  • 22. Diphenoxylate: 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. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 23. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins Question • Signs of atropine toxicity includes which of the following? – A. Dry mouth – B. Hypothermia – C. Tachycardia – D. Urinary retention – E. All of the above
  • 24. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins Answer • 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.
  • 25. 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) Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 26. 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 Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 27. 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 Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 28. 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. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins • Environment – Assess the environment where the drug will be given. • Culture and inherited traits – Cultural variations about frequency of bowel movements
  • 29. 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. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 30. Magnesium 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. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 31. Magnesium 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. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 32. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins Question • Magnesium hydroxide is a laxative that can be used for long-term therapy. – A. True – B. False
  • 33. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins Answer • B. False • Rationale: Magnesium hydroxide is not for long-term use. Fluid and electrolyte imbalance can occur with large doses given frequently.
  • 34. 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) Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 35. 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 Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 36. 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. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 37. Alosetron: Core Patient Variables • Health status – Assess type of IBS. • Life span and gender – Pregnancy Category B drug Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 38. 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. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 39. Alosetron: 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. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 40. Alosetron: 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. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 41. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins Question • What is the major adverse effect of alosetron? – A. Diarrhea – B. Constipation – C. Tachycardia – D. Nephrotoxicity
  • 42. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins Answer • B. Constipation • Rationale: Alosetron’s major adverse effect is constipation.
  • 43. 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) Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 44. 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. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 45. 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 Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 46. Mesalamine: Core Patient Variables • Health status – Assess for hypersensitivity. • Life span and gender – Pregnancy Category B drug Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 47. 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. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 48. Mesalamine: 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. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 49. Mesalamine: Teaching, Assessment, and Evaluation • Patient and family education – Educate the patient about the potential adverse Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 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.
  • 50. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins Question • Mesalamine may be prescribed for all age groups. – A. True – B. False
  • 51. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins Answer • B. False • Rationale: Mesalamine is not approved for use in children.