There can be variation in the licensing of
different medicines containing the same drug.
Tablet
▶Imodium Plus (McNeil Products Ltd)
Loperamide hydrochloride 2 mg, Dimeticone (as Simeticone)
125 mg
Imodium Plus caplets | 12 tablet p £4.21 DT = £4.21
Disorders of gastric acid
and ulceration
4.1 Dyspepsia
Dyspepsia
Description of condition
Dyspepsia describes a range of upper gastro-intestinal
symptoms, which are typically present for 4 or more weeks.
Symptoms include but are not limited to upper abdominal
pain or discomfort, heartburn, gastric reflux, bloating,
nausea and/or vomiting. Symptoms can be attributed to an
underlying cause (e.g. Gastro-oesophageal reflux disease
p. 88, Peptic ulcer disease p. 76, gastro-oesophageal
malignancy, or side effects from drugs), but the majority of
patients are likely to have functional dyspepsia, where an
underlying cause cannot be identified and endoscopy
findings are normal. Uninvestigated dyspepsia describes
symptoms in patients who have not had an endoscopy.
Dyspepsia symptoms in pregnancy are commonly due to
gastro-oesophageal reflux disease (GORD), for management
see GORD in pregnancy in Gastro-oesophageal reflux disease
p. 88.
Aims of treatment
The aim of treatment is to manage symptoms, and where
possible, to treat the underlying cause of dyspepsia.
Non-drug treatment
g Lifestyle measures, such as healthy eating, weight loss
(if obese), avoiding any trigger foods, eating smaller meals,
eating the evening meal 3–4 hours before going to bed,
raising the head of the bed, Smoking cessation p. 520, and
reducing alcohol consumption may improve symptoms.
Assess the patient for stress, anxiety, or depression, as these
conditions may exacerbate symptoms.
Urgent endoscopic investigation is required for patients
with dysphagia, significant acute gastrointestinal bleeding,
or in those aged 55 years and over with unexplained weight
loss and symptoms of upper abdominal pain, reflux or
dyspepsia. h
Drug treatment
g Drugs that may cause dyspepsia, such as alpha-
blockers, antimuscarinics, aspirin, benzodiazepines, beta-
blockers, bisphosphonates, calcium-channel blockers,
corticosteroids, nitrates, non-steroidal anti-inflammatory
drugs (NSAIDs), theophyllines, and tricyclic antidepressants,
should be reviewed. The lowest effective dose should be used
and if possible, stopped.
Antacids and/or alginates may be used for short-term
symptom control, but long-term, continuous use is not
recommended. h
Initial management
Uninvestigated dyspepsia
g A proton pump inhibitor should be taken for 4 weeks.
Patients with dyspepsia should be tested for Helicobacter
pylori (H. pylori) infection, and treated if positive. h Public
Health England recommends that patients who are at high
risk for H. pylori infection should be tested for H. pylori first,
or in parallel with a course of proton pump inhibitor. For
treatment regimens, see Helicobacter pylori infection p. 89.
Functional dyspepsia
g Patients should be tested for H. pylori infection and
treated if positive. See Helicobacter pylori infection p. 89 for
testing and management of H. pylori infection. In patients
not infected with H. pylori, a proton pump inhibitor or a
histamine2-receptor antagonist (H2-receptor antagonist)
should be taken for 4 weeks. h
Follow up management
Uninvestigated and functional dyspepsia
g For patients with refractory dyspepsia symptoms, new
alarm symptoms should be assessed and alternative
diagnoses should be considered. The patient’s adherence to
initial management should be checked and lifestyle advice
reinforced.
If symptoms persist or recur following initial management,
a proton pump inhibitor or H2-receptor antagonist therapy
should be used at the lowest dose needed to control
symptoms. The patient may use the treatment on an ’as-
needed’ basis.
In patients with uninvestigated dyspepsia taking an NSAID
and unable to stop the drug, consider reducing the NSAID
dose and using long-term gastro-protection with acid
suppression therapy, or switching to an alternative to the
NSAID, such as paracetamol p. 465 or a selective cyclo-
oxygenase (COX)-2 inhibitor (but see Cardiovascular Events
under Non-steroidal anti-inflammatory drugs p. 1193).
In patients with uninvestigated dyspepsia taking aspirin
and unable to stop the drug, consider switching from aspirin
to an alternative antiplatelet drug.
Patients treated with H. pylori eradication therapy do not
require routine retesting. h There are specific situations
where retesting may be appropriate, see Retesting for
Helicobacter pylori, under Helicobacter pylori infection p. 89.
g If retesting is positive, second-line eradication therapy
should be prescribed.
An annual review should be performed for patients with
dyspepsia to assess their symptoms and treatment. A ’step
down’ approach, or stopping treatment, should be
encouraged if possible and clinically appropriate. A return to
self-treatment with antacid and/or alginate therapy may be
Gastro-intestinal system
appropriate.
Referral to a specialist for further investigations should
occur in patients of any age with gastro-oesophageal
symptoms that are unexplained or non-responsive to
treatment, or in patients with H. pylori infection that has not
responded to second-line eradication therapy—see
Helicobacter pylori infection p. 89. h
Useful Resources
Gastro-oesophageal reflux disease and dyspepsia in adults:
investigation and management. National Institute for Health
and Care Excellence. NICE guideline 184. September 2014,
reviewed October 2019.
www.nice.org.uk/guidance/cg184
ANTACIDS
Antacids
Overview
Antacids (usually containing aluminium or magnesium
compounds) can often relieve symptoms in ulcer dyspepsia
and in non-erosive gastro-oesophageal reflux ; they are also
sometimes used in functional (non-ulcer) dyspepsia but the
evidence of benefit is uncertain. Antacids are best given
when symptoms occur or are expected, usually between
meals and at bedtime, although additional doses may be
required. Conventional doses of liquid magnesium–
aluminium antacids promote ulcer healing, but less well
than antisecretory drugs; proof of a relationship between
healing and neutralising capacity is lacking. Liquid
preparations are more effective than tablet preparations.
Aluminium- and magnesium-containing antacids (e.g.
aluminium hydroxide, magnesium carbonate p. 75, co-
magaldrox p. 74 and magnesium trisilicate p. 75), being
relatively insoluble in water, are long-acting if retained in
the stomach. They are suitable for most antacid purposes.
Magnesium-containing antacids tend to be laxative whereas
aluminium-containing antacids may be constipating;
antacids containing both magnesium and aluminium may
reduce these colonic side-effects. Aluminium accumulation
does not appear to be a risk if renal function is normal.
The acid-neutralising capacity of preparations that
contain more than one antacid may be the same as simpler
preparations. Complexes such as hydrotalcite confer no
special advantage.
Sodium bicarbonate p. 1099 should no longer be
prescribed alone for the relief of dyspepsia but it is present
as an ingredient in many indigestion remedies. However, it
retains a place in the management of urinary-tract disorders
and acidosis.
Bismuth-containing antacids (unless chelates) are not
recommended because absorbed bismuth can be neurotoxic,
causing encephalopathy; they tend to be constipating.
Calcium-containing antacids can induce rebound acid
secretion: with modest doses the clinical significance is
doubtful, but prolonged high doses also cause
hypercalcaemia and alkalosis, and can precipitate the milk-
alkali syndrome.
Simeticone
Simeticone p. 76 (activated dimeticone) is added to an
antacid as an antifoaming agent to relieve flatulence. These
preparations may be useful for the relief of hiccup in
palliative care.
Alginates
Alginates taken in combination with an antacid increases
Gastro-intestinal system
the viscosity of stomach contents and can protect the
oesophageal mucosa from acid reflux. Some alginate-
containing preparations form a viscous gel (‘raft’) that floats
on the surface of the stomach contents, thereby reducing
symptoms of reflux.
The amount of additional ingredient or antacid in
individual preparations varies widely, as does their sodium
content, so that preparations may not be freely
interchangeable.
ANTACIDS › ALGINATE
PDF pages 94, 95, 96