This site is intended for healthcare professionals

Go to /sign-in page

You can view 5 more pages before signing in

Go to /pro/cpd-dashboard page

This page is worth 0.05 CPD credits. CPD dashboard

Go to /account/subscription-details page

This page is worth 0.05 CPD credits. Upgrade to Pro

NICE guidance - management of dyspepsia in adults in primary care (summary section)

Authoring team

Summary points from the NICE guideline on the management of dyspepsia are presented below:

Referral for endoscopy

  • review medications for possible causes of dyspepsia (for example, calcium antagonists, nitrates, theophyllines, bisphosphonates, corticosteroids and non-steroidal anti-inflammatory drugs [NSAIDs]). In patients requiring referral, suspend NSAID use
  • NICE cancer referral guidance states (2):
    • Suspected Oesophageal cancer Suspected Stomach cancer Non Urgent Referral guidance: Suspected stomach cancer/oesophageal cancer:
      • offer urgent direct access upper gastrointestinal endoscopy (to be performed within 2 weeks) to assess for oesophageal cancer n people:
        • with dysphagia or
        • aged 55 and over with weight loss and any of the following:
          • upper abdominal pain
          • reflux
          • dyspepsia
      • consider a suspected cancer pathway referral (for an appointment within 2 weeks) for people with an upper abdominal mass consistent with stomach cancer
      • offer urgent direct access upper gastrointestinal endoscopy (to be performed within 2 weeks) to assess for stomach cancer in people:
        • with dysphagia or
        • aged 55 and over with weight loss and any of the following:
          • upper abdominal pain
          • reflux
          • dyspepsia
      • consider non-urgent direct access upper gastrointestinal endoscopy to assess for stomach cancer/oesophageal cancer in people with haematemesis

      • consider non-urgent direct access upper gastrointestinal endoscopy to assess for stomach cancer/oesophageal cancer in people aged 55 or over with:
        • treatment-resistant dyspepsia or

        • upper abdominal pain with low haemoglobin levels or

        • raised platelet count with any of the following:
          • nausea
          • vomiting
          • weight loss
          • reflux
          • dyspepsia
          • upper abdominal pain, or

        • nausea or vomiting with any of the following:
          • weight loss
          • reflux
          • dyspepsia
          • upper abdominal pain

Interventions for uninvestigated dyspepsia

  • initial therapeutic strategies for dyspepsia are empirical treatment with a proton pump inhibitor (PPI) or testing for and treating H. pylori
  • there is currently insufficient evidence to guide which should be offered first
  • a 2- week washout period following PPI use is necessary before testing for H. pylori with a breath test or a stool antigen test

Interventions for gastro-oesophageal reflux disease (GORD)

  • offer people a full-dose PPI (see table 1 in notes) for 8 weeks to heal severe oesophagitis, taking into account the person's preference and clinical circumstances (for example, underlying health conditions and possible interactions with other drugs).
  • offer a full-dose PPI (see notes) long-term as maintenance treatment for people with severe oesophagitis, taking into account the person's preference and clinical circumstances (for example, tolerability of the PPI, underlying health conditions and possible interactions with other drugs), and the acquisition cost of the PPI
  • do not routinely offer endoscopy to diagnose Barrett's oesophagus, but consider it if the person has GORD. Discuss the person's preferences and their individual risk factors (for example, long duration of symptoms, increased frequency of symptoms, previous oesophagitis, previous hiatus hernia, oesophageal stricture or oesophageal ulcers, or male gender).

Interventions for peptic ulcer disease

  • offer H pylori eradication therapy to people who have tested positive for H pylori and who have peptic ulcer disease
  • for people using NSAIDs with diagnosed peptic ulcer, stop the use of NSAIDs where possible. Offer full-dose PPI (see table 2) or H2RA therapy for 8 weeks and, if H pylori is present, subsequently offer eradication therapy
  • offer people with peptic ulcer (gastric or duodenal) and H pylori retesting for H pylori 6 to 8 weeks after beginning treatment, depending on the size of the lesion

Interventions for functional dyspepsia

  • management of endoscopically determined non-ulcer dyspepsia involves initial treatment for H. pylori if present, followed by symptomatic management and periodic monitoring
  • re-testing after eradication should not be offered routinely, although the information it provides may be valued by individual patients

Referral to a specialist service

  • consider referral to a specialist service for people:
    • of any age with gastro-oesophageal symptoms that are non-responsive to treatment or unexplained
    • with suspected GORD who are thinking about surgery
    • with H pylori that has not responded to second-line eradication therapy

Reviewing patient care

  • offer patients requiring long-term management of symptoms for dyspepsia an annual review of their condition, encouraging them to try stepping down or stopping treatment
  • a return to self-treatment with antacid and/or alginate therapy (either prescribed or purchased over-the-counter and taken as required) may be appropriate

H. pylori testing and eradication

  • H. pylori can be initially detected using either a carbon-13 urea breath test or a stool antigen test, or laboratory-based serology where its performance has been locally validated. Office-based serological tests for H. pylori cannot be recommended because of their inadequate performance
  • for patients who test positive, provide a 7-day, twice-daily course of treatment consisting of a full-dose PPI with additional medication as described in linked item

For full details then refer to the full guideline (1).

Notes:

Table 1: PPI doses for severe oesophagitis

PPI

Full/Standard dose

Low dose (on demand dose)

Double dose

Esomeprazole

40 mg once a day

20mg once a day

40 mg twice a day

Lansoprazole

30mg once a day

15mg per day

30 mg twice a day

Omeprazole

40 mg once a day

20mg per day

40 mg twice a day

Pantoprazole

40 mg once a day

20mg per day

40mg twice a day

Rabeprazole

20mg once a day

10mg per day

20mg twice a day

Table 2: PPI doses for peptic ulcer disease

PPI

Full/Standard dose

Low dose (on demand dose)

Double dose

Esomeprazole

20 mg* once a day

Not available

40 mg*** once a day

Lansoprazole

30mg once a day

15mg per day

30 mg** twice a day

Omeprazole

20 mg once a day

10mg* per day

40 mg once a day

Pantoprazole

40 mg once a day

20mg per day

40mg twice a day

Rabeprazole

20mg once a day

10mg per day

20mg twice a day

* lower than the licensed starting dose for esomeprazole in GORD, which is 40 mg, but considered to be dose-equivalent to other PPIs. When undertaking meta-analysis of dose related effects, NICE classed esomeprazole 20 mg as a full-dose equivalent to omeprazole 20 mg

**Off-label dose for GORD

***40 mg is recommended as a double dose of esomeprazole because the 20-mg dose is considered equivalent to omeprazole 20 mg.

 

Reference:

  1. Gastro-oesophageal reflux disease and dyspepsia in adults: investigation and management. NICE Clinical Guideline (Sept 2014 - last updated October 2019)
  2. National Institute for Health and Care Excellence. Suspected cancer: recognition and referral. Oct 2023 [internet publication].

Create an account to add page annotations

Annotations allow you to add information to this page that would be handy to have on hand during a consultation. E.g. a website or number. This information will always show when you visit this page.

The content herein is provided for informational purposes and does not replace the need to apply professional clinical judgement when diagnosing or treating any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions.

Connect

Copyright 2024 Oxbridge Solutions Limited, a subsidiary of OmniaMed Communications Limited. All rights reserved. Any distribution or duplication of the information contained herein is strictly prohibited. Oxbridge Solutions receives funding from advertising but maintains editorial independence.