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Overview
The symptoms of dyspepsia (including bloating, heartburn, and abdominal
pain) tend to wax and wane and, in many cases, they may be worsened by stress
or particular foods. Thus, many people do not need any medication or, at
least, regular medication to deal with their symptoms. However, for many
others, even reassurance that there is no serious underlying disease and
close attention to diet and lifestyle do not provide adequate symptom relief.
Discussions
of treatment options (including lifestyle modifications and surgery) for
specific conditions (i.e. gallstones, GERD, gastroparesis/ dysmotility,
Helicobacter pylori infection, etc.) can be found in the pages that address
particular disorders. The following is a description of different medical
treatments available for the symptoms of dyspepsia. Many of these treatments
may also be used for GERD and other conditions which cause symptoms of
dyspepsia. These treatments fall into several groups.
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Antacids
These medications contain one or more compounds based on calcium, magnesium,
aluminium or sodium bicarbonate. They work by neutralising gastric acid
in the stomach or, in patients with reflux disease, in the esophagus.
Some antacids are also combined with another compound, such as an alginate,
which is intended to coat and protect the lining of the esophagus and
stomach.
Antacids
can be bought 'over-the-counter' (OTC), without a doctor's prescription.
If used in accordance with the instructions, they are safe although some
may cause diarrhea, some may cause constipation and some should be used
with caution by people with kidney problems.
Antacids
often provide rapid relief, particularly for milder symptoms, but they
have not been shown to be effective in the long run for dyspepsia, reflux
disease or peptic ulcer disease. In addition, they must be taken frequently,
up to 4 to 7 times per day, for more severe symptoms.
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Acid
secretion blockers
There are two types of medication which reduce acid secretion: H2-blockers
(histamine H2-receptor antagonists) and PPIs (proton
pump inhibitors).
H2-blockers
These medications work by blocking the effect of histamine (a chemical
secreted in the stomach) which would normally stimulate the parietal cells
in the stomach to produce gastric acid. The first H2-blocker,
cimetidine (Tagemet®) become available 25 years ago and it was followed
by ranitidine (Zantac®), famotidine (Pepcid®) and nizatidine (Axid®).
H2-blockers are all available as prescription medications
and some are available in lower dose, 'over-the-counter' (OTC), without
a doctor's prescription.
H2-blockers are generally very safe and they are
effective for mild to moderate reflux disease (GERD) and, possibly, for
dyspepsia but they are less effective than proton pump inhibitors. They
are usually taken twice daily although, in some cases, as single night-time
dose may be effective.
Proton
Pump Inhibitors
These medications work by blocking the enzyme (H+-K+ ATPase) in the parietal
cells which secrete acid into the stomach. They are much more effective
at reducing acid secretion than H2-blockers and
they have been shown to be effective than H2-blockers
for the treatment of gastroesophageal reflux disease (GERD), peptic ulcer
and non-ulcer dyspepsia. The first PPI, omeprazole (Losec®, Prilosec®,
Antra®) was introduced 10-15 years ago and has been followed by lansoprazole
(Prevacid®), pantoprazole (Pantoloc®, Protonix®), rabeprazole
(AcipHex®, Pariet®) and esomeprazole (Nexium®). PPIs are available
only as prescription medications. PPIs are generally very safe and they
are effective for gastroesophageal reflux disease (GERD), peptic ulcer
disease and dyspepsia; in combination with antibiotics, they are also
very effective for curing Helicobacter pylori infection in patients with
peptic ulcer disease and dyspepsia.
PPIs are usually taken once daily (in the morning, about 30 minutes before
breakfast) although, in some cases, as second dose (before the evening
meal) may be necessary.
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Motility
agents
A high proportion of people with dyspepsia have symptoms which suggest
an abnormality of motility (contractions) in the stomach or small intestine.
Some of these patients will improve with medications which can regulate
gastrointestinal motility - these are often known as 'prokinetic' or promotility'
agents.
Metoclopramide
(Maxeran®, Maxolon®, Reglan®)
This medication can help relieve nausea and improve gastric emptying.
It is useful in a small proportion of patients but it can also have side
effects in some. It is not used widely for dyspepsia. It is usually taken
3 to 4 times daily, before meals.
Domperidone
(Motilium®)
This medication can help relieve dyspeptic symptoms and improve gastric
emptying. It is useful in a proportion of patients but it is generally
safe although it can cause a (benign) discharge from the breasts: the
discharge stops when the medication is stopped. It is usually taken 3
to 4 times daily, before meals.
Cisapride
(Prepulsid®, Propulsid®)
This medication can relieve dyspeptic symptoms and improve gastric emptying.
It is the best documented and most effective of the motility agents but
it has been withdrawn from general use in most countries because of rare
heart rhythm irregularites. It is usually taken 3 to 4 times daily, before
meals.
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Protective agents
Sucralfate
(Sulcrate®)
This medication is a complex of sucrose and aluminium. It has been used
to treat peptic ulcer and, occasionally, esophagitis. The precise mechanism
of action is not known and it is not widely used. It is usually taken
4 times daily.
Misoprostol
(Cytotec®)
This medication belongs to a class of medications known as prostaglandin
analogues. It reduces gastric acid secretion but is less effective than
H2-blockers or PPIs; it also provides some protection against damage caused
by other agents such as arthritis medications (NSAIDs - non-steroidal
anti-inflammatory drugs; ASA - acetylsalicylic acid). Most commonly, it
is used to reduce the development of ulcers in patients who need to continue
taking NSAIDs. It is generally used for normal peptic ulcer disease or
reflux disease. It can cause abdominal cramps and diarrhoea and it should
not be taken during pregnancy as it can cause abortion. It is usually
taken 2 to 4 times daily.
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Helicobacter pylori eradication therapy
Cure of H.
pylori cures peptic ulcer disease in most patients and
prevents recurrent complications such as bleeding or perforation. It has
also been shown to produce symptom relief in a proportion of patients
with non-ulcer dyspepsia or 'uninvestigated dyspepsia'. In the latter
case, patients with uninvestigated dyspepsia are those who have a positive
urea breath test but have not had an endoscopy to confirm peptic ulcer
disease.
PPI-Triple
Therapy
This is the most widely-used treatment combination: a PPI with two antibiotics,
taken twice daily. This treatment is generally taken for one week although
in some countries, a two-week course is recommended. The PPI can be omeprazole,
lansoprazole, pantoprazole, rabeprazole or esomeprazole; the antibiotics
are usually a combination of clarithromycin (Biaxin®) + metronidazole
(Flagyl®), amoxicillin (Amoxil®) or metronidazole (Flagyl®)
+ amoxicillin (Amoxil®). Other antibiotics, such as rifabutin, furazolidone
or tetracycline are used occasionally if PPI-triple therapy has not worked.
The cure rates with these combinations range from 80% to 90+%; side effects
include nausea, vomiting, a metallic taste in the mouth and diarrhoea.
Bismuth-Triple
Therapy
This was the one of the first combinations studied: it consists of a one-
to two-week course of bismuth (Pepto-Bismol®), metronidazole (Flagyl®)
and tetracycline, all taken four times daily. The cure rates with this
combination range from 80% to 90%; side effects include nausea, vomiting,
a metallic taste in the mouth, diarrhoea and black stools (which are not
due to bleeding). This combination requires the patients to take more
tablets (up to 16/day) than PPI-triple therapy and it is generally less
well-tolerated.
PPI-Bismuth
Quadruple Therapy
This combination is the same as Bismuth-triple therapy with the addition
of a PPI, taken twice daily. It is generally reserved for patients whose
infection has not been cured by one or two courses of a PPI-tripe regimen.
The cure rates with this combination range from 80% to 95%; side effects
include nausea, vomiting, a metallic taste in the mouth, diarrhoea and
black stools (which are not due to bleeding).
Ranitidine
bismuth citrate
Ranitidine bismuth citrate (Pylorid®) has been used in combination
with clarithromycin (Biaxin®) for two weeks and in combination with
clarithromycin (Biaxin®) + amoxicillin (Amoxil®) or metronidazole
(Flagyl®) for one week. The cure rates are comparable to those for
other combinations but it is not widely available.
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Other therapy
If dyspeptic symptoms have been shown not to be due to an underlying condition
such as reflux disease, ulcer disease, etc and, if first-line treatments,
listed above, are ineffective or inappropriate, treatment directed at
reducing stress, anxiety and depression may be helpful. Although there
are very few studies, antidepressants, such as amitriptylline or imipramine
and psychological intervention, such as cognitive behavioural therapy
may help.
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