Gastrointestinal tract (GIT) medications Flashcards

1
Q

Oral cavity

A

Substances enter the digestive system through the mouth. As food enters, the salivary glands release saliva, which mixes with the food to form a bolus (a wet mass). The mouth is the first site of chemical digestion, while chewing (mastication) breaks down food into smaller pieces for swallowing.

Drugs can enter the mouth as tablets, capsules, or liquids and are usually swallowed to enter the digestive tract. However, not all drugs are swallowed. Some, given by the buccal (inside the cheek) or sublingual (under the tongue) routes, are absorbed quickly through the mouth lining, bypassing the rest of the digestive system.

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2
Q

Oesophagus

A

The pharynx connects to the stomach through the esophagus, a long tube. Two muscular sphincters, at the top and bottom of the esophagus, open during swallowing to let food pass from the pharynx to the stomach.

The esophagus doesn’t play a big role in drug absorption. However, if the upper sphincter is weak or relaxed, stomach acid can flow back into the esophagus, causing heartburn or acid reflux. Some gastrointestinal medications are designed to neutralize this acid and relieve symptoms of reflux.

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3
Q

Stomach

A

When the bolus reaches the stomach, it is mixed with stomach secretions and broken down into chyme, a semifluid mass. While some protein and fat digestion happens here, very little absorption occurs in the stomach. After 2-6 hours, the chyme is slowly released into the small intestine.

The stomach lining has five types of cells that aid digestion. Four of them (surface mucous cells, mucous neck cells, parietal cells, and chief cells) produce gastric secretions, which include mucin (protects the stomach), intrinsic factor (helps absorb vitamin B12), hydrochloric acid, and pepsin. The fifth cell type, G cells, releases gastrin, which helps with stomach movement and secretion.

Though the stomach doesn’t absorb much food, it can absorb drugs, especially acidic ones like aspirin. To prevent disintegration in the stomach’s acidic environment, some drugs are enteric coated so they dissolve in the intestines instead. The speed at which the stomach empties can also impact how quickly a drug is absorbed, with faster emptying leading to quicker absorption.

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4
Q

Small intestine: Duodenum, jejunum and ileum

A

Chyme leaves the stomach in small amounts and enters the duodenum, the first part of the small intestine. In the small intestine, it mixes with bile and pancreatic juices from the gallbladder and pancreas. These secretions are controlled by two hormones, CCK and secretin. The chyme then moves to the jejunum for digestion and absorption, and this continues in the ileum, the last part of the small intestine.

Most drugs are absorbed in the intestines due to their large surface area. Food in the gut can affect drug absorption, which is why some drugs are taken before meals (for faster absorption) and others with food (to prevent stomach irritation). Gastrointestinal issues like vomiting, diarrhea, or constipation can also affect how well drugs are absorbed.

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5
Q

Large intestine

A

The watery chyme moves from the small intestine into the large intestine, which extends from the ileum to the anus. The large intestine includes the caecum, ascending colon, transverse colon, descending colon, sigmoid colon, rectum, and anus. Its main job is to absorb water and electrolytes (like sodium and chloride), turning the chyme into faeces. Bacteria in the large intestine help break down leftover carbohydrates, proteins, and fats.

Inflammation can change the structure and function of the gut wall, which may affect drug absorption, depending on the affected area. The GIT also plays a role in drug excretion, with some drugs being excreted in bile and removed with faeces.

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6
Q

Introducing solids/liquids into the oral cavity

A

Ingestion

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7
Q

Mixing and moving material through the GIT

A

Motility

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8
Q

Manufacturing and releasing substances that facilitate digestion

A

Secretion

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9
Q

Breaking down (mechanically or chemically) ingested food into smaller structures

A

Digestion

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10
Q

Transporting digested molecules, electrolytes, vitamins, water from the GIT into the blood or lymph

A

Absorption

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11
Q

Expelling indigestible or unabsorbed material

A

Elimination

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12
Q

An introduction to gastrointestinal tract conditions

A

Good bowel function relies on a diet with enough fiber, proper fluid intake, and regular physical activity, which may also help prevent some gastrointestinal diseases. Some GIT issues, like nausea, vomiting, diarrhea, and constipation, are temporary and linked to infections or diseases, while others are chronic and need ongoing treatment.

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13
Q

Nausea and vomiting

A

Definition

Nausea is an uneasiness of the stomach

Vomiting is the forcible voluntary or involuntary emptying of stomach contents through the mouth

Processes at play

Causes include food allergies, seasickness, morning sickness, GIT infections, and some medications, including cancer treatments

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14
Q

Gastric reflux (Heartburn)

A

Definition

Excessive activity of the stomach acid

Processes at play

Stomach produces hydrochloric acid or HCl and this acid flows up into the oesophagus

If prolonged is referred to as gastro-oesophageal-reflux disease (GORD)

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15
Q

Peptic ulcers

A

Definition

An erosion or break in the stomach mucosa - allows contacts between eroded area and the stomach’s acid (HCl)

Processes at play

Erosions may be caused by bacteria e.g. Helicobacter pylori (a spiral-shaped bacteria)

May occur from overproduction of acid (rare) e.g. from gastrin-producing tumours

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16
Q

Diarrhoea

A

Definition

An increase in number of stools (usually three or more per day) and passage of unformed faeces

Processes at play

Can be caused by a range of conditions/medical interventions including emotional stress, anxiety, colon disease (e.g. Crohn’s disease), food allergies or intolerances, intestinal infection, medications (e.g. iron, antibiotics), surgery of colon, enteral nutritional therapy

17
Q

Constipation

A

Definition

A decrease in frequency of normal bowel movements

Processes at play

Causes include low fibre diet, poor fluid intake, ignoring urge to defecate, cognitive disorders, neurological disorders

18
Q

Irritable bowel syndrome

A

Definition

A condition where the colon contracts more or less often than “normal”

Processes at play

Exact cause is unknown

May be associated with bacterial overgrowth, can develop after severe diarrhoea

19
Q

Colitis

A

Definition

A condition where the colon contracts more or less often than “normal”

Processes at play

Several types including ulcerative colitis, infectious colitis and Chron’s disease

20
Q

Colon polyps

A

Definition

Benign (non-cancerous) growths in the tissues of the lower GIT

Processes at play

Exact cause is unknown

21
Q

Colorectal (bowel) cancer

A

Definition

Abnormal cells develop and start to invade surrounding tissues of the lower GIT

Processes at play

Abnormal cancerous cells may develop from precancerous polyps

Risk factors for colorectal cancer include family history, diet low in fibre, lack of physical activity, obesity and high alcohol intake

22
Q

Upper gastrointestinal tract medications

A

Drugs used to treat gastric reflux and GORD include antacids, H2 receptor antagonists, and proton pump inhibitors (Bullock & Manias, 2022). Peptic ulcers are treated by antibiotics and other medications (such as proton pump inhibitors, antacids, and histamine H2 receptor antagonists) in order that the underlying infection can be eliminated, and the stomach acid minimises or neutralised to promote healing

23
Q

Histamine H2 antagonists

A

Examples

Ranitidine (Zantac)
Nizatidine (Tazac)
Famotidine (Ausfam)
NB: Cimetidine (Tagamet) was a commonly used H2 antagonists however it was removed from the Australian Register of Therapeutic Goods in July 2022 (Health Direct, 2022).

Action

Block the release of gastric acid

Processes at play

H2 receptor antagonists target the three receptors in the stomach wall responsible for stomach acid production (histamine H2 receptors, muscarinic receptors and gastrin receptors).
By interacting with the receptors, histamine H2 receptor antagonists block the production of stomach acid.

Important nursing knowledge

Long term side effects of medications that influence stomach acid levels is disruption of the absorption of various substances in the stomach (such as vitamin B12 and magnesium).
Regular testing of these substances in the blood and possible supplementation of these substances may be required
Administration is not affected by food.

24
Q

Antacids

A

Examples

Mylanta
Gaviscon

Action

Combine with hydrochloric acid and neutralise it

Indication / Processes at play

Made from magnesium hydroxide and aluminium hydroxide (weak bases)

Important nursing knowledge

Antacids may interact with the absorption (and therefore impact) of other medications
Take 2 hours before or after other medications.

25
Q

Proton pump inhibitors

A

Examples

Omeprazole (Losec)

Action

Reduce the production of hydrochloric acid

Processes at play

Inhibit the production of the hydrogen (H+) proton needed to make it

Important nursing knowledge

Side effects include dry mouth, nausea, vomiting and abdominal discomfort
Increases the risk of developing upper respiratory tract infections.

26
Q

Serotonin antagonists

A

Examples

Ondansetron (Zofran)

Action

Blocks the HT3 receptor

Indication

Anti-emetic (stops nausea and vomiting)

Important nursing knowledge

Side effects include confusion, dizziness, tachycardia

27
Q

Lower gastrointestinal tract medications

A

Constipation is also caused by a range of conditions and is a side effect of many medications. Laxatives (also called aperients) are medications used to ease constipation and they are grouped into categories based on their mode of action

28
Q

Osmotic laxatives

A

Method of action

Water is retained, or even pulled back into the colon through osmosis

Examples

Glycerol
Lactulose

Onset of action

24 - 72 hours

29
Q

Faecal softener

A

Method of action

Hold water molecules in the faecal matter, rendering them softer and easier to pass

Examples

Docusate (Coloxyl)

Paraffin (Agarol)

Onset of action

24 - 72 hours

30
Q

Stimulant laxatives

A

Method of action

Causes an increase in peristalsis by irritating the smooth muscle of the intestinal wall

Examples

Caster oil
Sennosides

Onset of action

6 - 12 hours

31
Q

Bulk forming laxatives

A

Method of action

Dietary fibre, found in the outer coatings of seeds and grains is not digestible in humans

This adds bulk to the colonic contents, which stimulates movements and the defecation reflex

Examples

Fybogel

Metamucil

Onset of action

48 - 72 hours

32
Q

What is an aperient?

A

An aperient (also termed a laxative) is a medication used in the management of constipation.

33
Q

Aperients can be classified into four (4) groups based on their mode of action.
Name the four types of aperients.

A
  1. Osmotic laxatives
  2. Stimulant laxatives
  3. Faecal softeners
  4. Bulk forming laxatives
34
Q

What is the mechanism of action of an osmotic laxative?

A

An osmotic laxative draws water into the colon by osmosis, softens stool and increases peristalsis.

35
Q

What is the mechanism of action of a stimulant laxative?

A

A stimulant laxative increases peristalsis by irritating smooth muscles of the intestinal wall.

36
Q

What is the mechanism of action of a faecal (stool) softener?

A

A stool softener holds water molecules in faecal matter to soften faeces and allow it to pass.

37
Q

What is the mechanism of action of a bulk forming laxative?

A

A bulk forming laxative adds bulk to colonic contents and stimulates peristalsis and reduces transit time.