Management of gastro-oesophageal reflux disease in general practiceBMJ 2001; 322 doi: https://doi.org/10.1136/bmj.322.7282.344 (Published 10 February 2001) Cite this as: BMJ 2001;322:344
- John Dent, professor of medicinea,
- Roger Jones (), professor of general practiceb,
- Peter Kahrilas, professor of medicinec,
- Nicholas J Talley, professor of medicined
- a Department of Gastroenterology, Hepatology, and General Medicine, Royal Adelaide Hospital, Adelaide, SA 5000, Australia
- b Department of General Practice and Primary Care, Guy's, King's, and St Thomas' School of Medicine, London SE11 6SP
- c Division of Gastroenterology and Hepatology, Department of Medicine, Northwestern University Medical School, Chicago, IL 60611-3008, USA
- d Department of Medicine, University of Sydney, Nepean Hospital, Penrith, PO Box 63, NSW 2751, Australia
- Correspondence to: R Jones
- Accepted 3 January 2001
Gastro-oesophageal reflux disease is a potentially serious condition that can greatly reduce patients' quality of life and carries a risk of oesophagitis and complications.1 It is a common condition and a considerable burden on healthcare resources. Most patients are managed in general practice, and effective management of the disease remains a challenge. Guidelines produced in Europe, 2 3 the United States,4 and Canada5 do not give consistent recommendations.
Careful analysis of symptoms and history is key to diagnosis of gastro-oesophageal reflux disease
Diagnosis based on symptoms can be aided by a trial of treatment
Clear endoscopic abnormalities are found in less than half of patients
Treatment should start with the most effective therapy—a proton pump inhibitor
Most patients will require long term management, for which the guiding principle is to reduce to the least costly treatment that is effective in controlling symptoms
Antireflux surgery may be as effective as long term proton pump inhibitors but is less predictable
An international multidisciplinary workshop was held in Genval, Belgium, in 1999 to evaluate the literature on gastro-oesophageal reflux disease, including numerous reviews,6–8 in the light of clinical experience.9 Participants voted on their level of support and the strength of the evidence for a series of statements relevant to the management of the disease. In this article we summarise the conclusions of the Genval workshop and present an overview of the latest thinking on the management of gastro-oesophageal reflux disease relevant to general practice. We also reviewed relevant articles published since the workshop, which we identified by a search of the electronic databases Medline and Embase from 1997 to March 2000, using the search term gastro-oesophageal reflux in combination with various key words for drug therapy, surgery, cost effectiveness, and quality of life.
Definition of gastro-oesophageal reflux
Gastro-oesophageal reflux disease should be diagnosed in all patients who are at risk of physical complications from gastro-oesophageal reflux or whose wellbeing is appreciably impaired because of symptoms related to reflux. 7 9 Most patients do not have endoscopically visible lesions, and symptoms are the main consideration. Heartburn is the predominant symptom of gastro-oesophageal reflux disease, and patients' quality of life is impaired in proportion to the frequency and severity of heartburn,9 irrespective of the presence or severity of oesophagitis. The impact of symptoms on quality of life is similar to that of symptoms of other disorders such as ischaemic heart disease.10 A recent large study using the SF-36 questionnaire showed the negative effect of gastro-oesophageal reflux disease on quality of life, notably on measures of pain, mental health, and social function.11 Symptoms are mainly due to the oesophageal mucosa being exposed to acid and pepsin, and some patients may have a more sensitive mucosa than others.
How reliable is diagnosis based on symptoms and what can be done to aid it?
Although gastro-oesophageal reflux disease is still commonly misdiagnosed as dyspepsia, the two problems are distinct and require different management. The Rome II working group defined dyspepsia as pain or discomfort centred in the upper abdomen.12 This definition excludes heartburn, the primary symptom of gastro-oesophageal reflux disease. Careful analysis of the patient's symptoms and history is pivotal in the diagnosis and subsequent management of gastro-oesophageal reflux disease. Recognition of alarm symptoms (see box on endoscopy) is important in determining the need for referral.
Diagnosis of gastro-oesophageal reflux disease is usually based on the occurrence of heartburn on two or more days a week, although less frequent symptoms do not preclude disease. 9 13 A standard against which to compare heartburn is still lacking for patients without oesophagitis. 7 9 Nevertheless, when heartburn is carefully defined, it is unlikely to be due to anything other than gastro-oesophageal reflux disease; indirect evidence and clinical experience show that three quarters of patients in whom heartburn is the main or sole symptom have gastro-oesophageal reflux disease.9 When inquiring about patients' symptoms it is important to give a definition of heartburn. For example, the description of heartburn as “a burning feeling rising from the stomach or lower chest up towards the neck” has been found to identify more patients with gastro-oesophageal reflux disease than use of the word itself. 9 14 Diagnosis may be improved by the use of a structured diagnostic questionnaire or by a trial of treatment, as described below.
When should patients be referred for endoscopy?
Less than half of patients with gastro-oesophageal reflux disease have diagnostic endoscopic abnormalities, and endoscopy therefore has a limited role in diagnosis. Endoscopy is, however, useful in some patients for clarification of diagnosis, assessing severity of disease, recognition of the complications of oesophagitis, and for defining best treatment strategies (box). No consensus exists on its precise role or on when it is best performed. 15 16 The use of endoscopy will depend on local cost, accessibility, and timing relative to treatment. Most patients should be managed empirically, at least initially.
Indications for early endoscopy
Alarm symptoms (including dysphagia, weight loss, bleeding, abdominal mass)
Diagnostic problems such as atypical symptoms
Symptoms refractory to initial treatment
Provision of reassurance when verbal reassurance is inadequate
Endoscopy may also be appropriate:
For patients who have had frequent, troublesome symptoms for a long time
To tailor drug treatment
To detect and manage Barrett's oesophagus
The questions of whether to look for Barrett's oesophagus, and what to do when it is found, are controversial and difficult.17 Affected patients have an increased risk of oesophageal adenocarcinoma, but views on surveillance vary widely. If patients are known to have Barrett's oesophagus, surveillance endoscopy is probably advisable. General practitioners should be guided by the opinion of a gastroenterologist.17 More information is available in the current practice guidelines.18
The results of endoscopy need to be reported in a standardised, defined language that is explicit and unambiguous. The report should explain the implications of the findings for patient care and, in particular, be sceptical about the diagnostic validity of minimal endoscopic changes (erythema, oedema, friability). We recommend the Los Angeles classification for endoscopic assessment and reporting of oesophagitis. 9 19 20 In addition, the possible effects of treatment should be borne in mind when interpreting the results of endoscopy. Repeat endoscopy is rarely justified in patients without severe oesophagitis. Monitoring of oeosphageal pH should be reserved for patients in whom the diagnosis is in doubt after endoscopy and a trial of acid suppressing drugs.
Effectiveness of different drugs
The hierarchy of efficacy of therapies in gastro-oesophageal reflux disease (box) has been well established in randomised clinical trials,9 although data on half dose proton pump inhibitors relate to its use in long term intermittent therapy rather than initial therapy. 9 21 22 The relative effectiveness is unaffected by the presence of endoscopic oesophagitis or whether treatment is short or long term. Long term safety and tolerability have been extensively documented for H2 receptor antagonists and proton pump inhibitors.23
Hierarchy of efficacy for drug treatments (most effective first)9
High dose proton pump inhibitors
Standard dose proton pump inhibitors
Half dose proton pump inhibitors
Standard dose H2-receptor antagonists
Cisapride has similar effectiveness to standard dose H2 receptor antagonists but is inferior to standard dose omeprazole.24 When combined with an H2 receptor antagonist, it is more effective than either treatment alone,25 but the risks of cardiac side effects with cisapride now exclude it from routine use in reflux disease.
Strategies for initial treatment
Explanation of the symptoms and reassurance of the patient (for example, addressing concerns about cancer and heart disease) are an important part of initial treatment. General practitioners should also consider lifestyle measures and self treatment, such as antacids, which the patient may already be using. Some lifestyle measures provide limited benefit in gastro-oesophageal reflux disease. Avoidance of specific foods and drinks that exacerbate symptoms may help, although it does not usually result in healing of the oesophagitis.9 Although stopping smoking and losing weight are of benefit to the patient's general health, they have little or no effect on gastro-oesophageal reflux disease.
There are two approaches to the initial medical treatment of gastro-oesophageal reflux disease. Treatment can either start with the most effective regimen and subsequently be stepped down or start with the minimum intervention and be stepped up. There are arguments in favour of both approaches (box). The higher initial drug cost when beginning with the most effective regimen is likely to be offset by rapid symptom control, which is a substantial benefit to the patient and reduces the need for repeated consultation. We recommend starting with the most effective treatment,9 which is currently standard dose of a proton pump inhibitor. This treatment is also the preferred choice for empirical therapy.
Advantages and disadvantages of step-down and step-up treatment
Although empirical therapy will test a provisional diagnosis, a formal therapeutic trial9 in which a proton pump inhibitor is given in greater than standard dose for 1-2 weeks can also be used. This test has a sensitivity and specificity for gastro-oesophageal reflux disease comparable to that of monitoring oesophageal pH.
After the initial treatment, it is worth trying a period without treatment because some patients will not need further medical intervention, at least for several months.26 Patients in whom symptoms immediately recur require longer term management.
Eradication of Helicobacter pylori does not heal oesophagitis or prevent relapse in patients with gastro-oesophageal reflux.9 However, there is likely to be a complex interaction between acid secretion, eradication of H pylori, and exposure of the oesophagus to acid in certain patients.
Strategies for long term management
Most patients with gastro-oesophageal reflux disease require long term management. 27 28 The guiding principle for long term management is to step down to the treatment that is least costly but still effective in controlling symptoms, following the hierarchy described above.9 The rationale for this approach is minimisation of cost, although relative drug costs will vary across practice settings, and decreasing efficacy does not always mean decreasing cost. Finding the right level of management may take time in some patients.
Patients returning with a relapse after a trial without treatment should be restarted on the initial successful therapy and then have treatment stepped down as appropriate. For patients who require only intermittent short courses of antisecretory therapy, it may be more effective to give a proton pump inhibitor at full dose than to titrate treatment up from either half dose of proton pump inhibitor or standard dose of a H2receptor antagonist.26
A further component in optimising use of resources is the minimal use of endoscopy. The success of a step down in treatment can largely be determined by symptoms alone. If a patient's symptoms are successfully controlled, the general practitioner can be confident that oesophagitis will have healed in most cases,9 and endoscopy is unnecessary. The comfort and convenience of patients are further reasons to minimise use of endoscopy.
The only patients in whom treatment should not be stepped down are those with severe oesophagitis (Los Angeles grades C and D). Treatment other than standard dose proton pump inhibitors is unlikely to prevent relapse of oesophagitis or strictures in these patients.9 Endoscopy is not always necessary as it is safe to assume that oesophagitis is healing in patients whose symptoms are controlled. Patients with inadequate symptom control should be referred for endoscopy.
Antireflux surgery is an attractive option for some patients as it can eliminate the need for life long drug treatment. It should not be reserved for patients in whom drugs have failed. Open antireflux surgery and long term proton pump inhibitors have been shown to be equally effective over a follow up of five years.29 Patients' preferences for medical or surgical treatment should be taken into account. Data on the safety of long term use of proton pump inhibitors suggest that this is safer option than antireflux surgery, which has a small but probably inevitable mortality of around 0.2% and appreciable morbidity. The laparoscopic approach, introduced 10 years ago, has superseded open antireflux surgery, but surgeons have to develop and maintain special skills to get consistently good results.30
We thank Tim Robinson for his contribution to an earlier draft of the paper.
Funding AstraZeneca provided support during the preparation of this manuscript.
Competing interests RJ has been sponsored to attend conferences and has received fees for speaking and consultancy from Wyeth, Glaxo Wellcome, and AstraZeneca. JD has received fees for doing clinical trials, speaking, organising educational activities from AstraZeneca, Lederle, and Janssen Pharmaceuticals. His basic science laboratory is involved in a collaborative research programme with AstraZeneca and receives partial funding for its work from this company. NJT has been a consultant for AstraZeneca, Janssen, and TAP and has research support from Lederle, Australia, and Pharmacia and Upjohn, Australia. PJK has been reimbursed by AstraZeneca, TAP, Janssen Pharmaceuticals, Wyeth-Ayerst Pharmaceuticals, and Merck Pharmaceuticals for lecturing and running educational programmes related to reflux disease.