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NURS G099 -Laxatives and Antidiarrheal Drug Therapy

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This is a comprehensive and detailed template on that contains vital info on; Laxatives and Antidiarrheal Drug Therapy.

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  • October 20, 2024
  • 15
  • 2020/2021
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Laxatives and Antidiarrheal Drug Therapy
Overview of Laxatives
 The irregular, sporadic, and strenuous passage of stool through the
lower gastrointestinal (GI) tract is defined as constipation.
 Laxatives are commonly used in the treatment of constipation.
 There are five types of laxatives, as shown in the table.
 Each laxative class has a differing mechanism of action; however, they
all assist in production of bowel movements (BMs).
 The main actions of laxatives are either aiding in fecal progression
through the colon, changing fecal firmness, or promoting the
elimination process through the rectum.
Class Mechanism of Action Examples: Generic
Osmotics (Saline) Draw water into the  Polyethylene glycol
intestine, which (PEG) or PEG with
relieves occasional electrolytes
constipation  Lactulose
 Glycerin
Stimulants (Contact or Stimulate intestinal  Bisacodyl
Irritants) walls, which causes the
muscles’ contraction to
clear the bowel
Bulk-Forming Soften and increase Psyllium
bulk of digested food,
so waste can more
easily travel through
and leave the body
Emollients (Stool Increase water in the  Docusate sodium
Softeners) stool, which helps  Docusate sodium
soften it and makes it with senna
more comfortable to  Docusate calcium
pass  Mineral oil
Selective Chloride Activate chloride Lubiprostone
Channel Activators channels in the small
intestine, which
enhances fluid
secretion and
movement in the
intestine

Pharmacokinetics of Laxatives
 Osmotics (Saline)
o Oral (PO) administration is the preferred method for saline
laxatives.
o Minimal absorption occurs, and excess is eliminated in the stool.
o The nonmetabolized portion is excreted in the urine.

, o Magnesium citrate, an often-used osmotic, binds to albumin and
globulins.
 Stimulants (contact or Irritants)
o Bisacodyl, the contact laxative, has minimal absorption from the
GI tract (<5%).
o Its volume of distribution is 289 L.
o The drug is metabolized to bis‐(p‐hydroxyphenyl)‐pyridyl‐2‐
methane (BHPM) in the colon, an active metabolite that is then
converted to a glucuronide salt in the liver.
o Elimination occurs in the feces, but a small portion is excreted in
urine.
 Bulk-Forming Laxatives
o Psyllium, a bulk-forming laxative (nonabsorbent and indigestible),
forms a sticky substance when combined with water.
o It is not absorbed, it does not have protein-binding properties,
metabolism is unknown, and it is eliminated in the feces
 Emollients (stool softeners)
o A small amount is absorbed from the GI tract with docusate.
o Docusate’s action occurs in the small and large intestines and
produces a BM with the first dose in 1 to 2 days but can also take
up to 3 to 5 days.
o Mineral oil is also an emollient whose onset of action is within 6 to
8 hours if taken orally, or 2 to 15 minutes if administered rectally.
o It is minimally absorbed and distributed into the intestinal mucosa,
liver, spleen, and mesenteric lymph nodes after being excreted via
the feces.
o Metabolism is unknown.
 Selective Chloride Channel Activators
o Lubiprostone has low systemic availability after PO administration
and is metabolized fast in the jejunum and stomach by carbonyl
reductase.
o Protein binding is 94%, and there is small dispersion beyond the
tissue of the GI tract.
o It is excreted in urine (60%) and feces (30%).

Pharmacodynamics of Osmotics (Saline)
 Glycerin, lactulose, saline products, and salts are considered osmotics,
which are hyperosmolar laxatives.
 Sodium or magnesium are in saline products, which are systemically
absorbed in small amounts.
 To avoid electrolyte imbalances, it is important to monitor electrolytes
in the blood.
 Fecal movement is enhanced when hyperosmolar salts bring water into
the colon, which increases the water content and promotes movement
through the colon.

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