The cost-effectiveness of screening for helicobacter pylori to reduce mortality and morbidity from gastric cancer and peptic ulcer disease: a discrete event simulation model
Roderick, P., Davies, R., Raftery, J., Crabbe, D., Pearce, R., Bhandari, P. and Patel, P. (2003) The cost-effectiveness of screening for helicobacter pylori to reduce mortality and morbidity from gastric cancer and peptic ulcer disease: a discrete event simulation model. Southampton, UK, National Coordinating Centre for Health Technology Assessments, 90pp. (Health Technology Assessment Series, (vol.7, pt.6) ).
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Aim/ principal research question:
To develop a discrete-event simulation model to evaluate the cost-effectiveness of population screening for H. pylori in England and Wales to prevent both gastric cancer and peptic ulcer disease.
Factors of interest:
Screening for H. pylori.
A model was developed using the ‘patient-oriented simulation technique’. In this model, without screening most H. pylori-positive individuals remained asymptomatic, but a proportion developed dyspepsia and presented to primary care where testing and eradication therapy could be given. H. pylori-positive individuals were assigned increased risks of developing peptic ulcer disease and gastric cancer. A proportion of peptic ulcer disease were fatal and most gastric cancers were incurable. In the screening scenarios, the population was invited to attend screening; those found to be H. pylori-positive were offered eradication therapy. For those accepting the risk of developing peptic ulcer was considered to reduce immediately to that of H. pylori-negative individuals. The effect of eradication on gastric cancer risk was modelled by assuming a time lag before such risk reverted to H. pylori-negative levels. The decline in gastric cancer incidence was taken into account by age cohort modelling.Key parameters were oH.pylori prevelence, relative risks of complicated peptic ulcer disease amd gastric cancer, screening accuracy and the efficacy of eradication therapy. UK data were used where available.
Costs were NHS costs based at year 2000 prices. Discounting used base rates of 6% for both costs and benefits. The model was run for an 80-year period for the base case, to allow the impact of screening on gastric cancer risk to accrue. Sensitivity analyses were performed, to explore different scenarios and where there was uncertainty about the estimated values used in the model. Both incident and prevalent screening rounds were modelled.
People in England and Wales.
There were four age-related scenarios: screen all people aged 20–49 as a prevalent round and then 20-year-olds for the next 20 years as an incident round; screen those aged 30–49 as a prevalent round and then 30-year-olds for 30 years as an incident round; screen those aged 40–49 as a prevalent round and then 40-year-olds for 40 years as an incident round, and finally screen all 50-year-olds for 50 years as an incident round.
Deaths, life years saved., cost per life year saved
Population screening would involve screening approximately 25 million individuals if uptake was 70%, with over 5 million people being treated. The number of deaths prevented falls with increasing age at screening, but so does the present value of costs because there would be less prevalent screening and costs are deferred.
In the base case the cost-effectiveness of H. pylori screening improves with age and is under £10,000 per life-year saved (LYS), for all age groups though over an 80-year period.. Screening at age 40 might be the most pragmatic policy, balancing cost-effectiveness and the feasibility of screening.
The cost/LYS for the base run at age 40 is £5866 falling to £1027 if the benefit is discounted at 1.5%. Screening by serology is more cost-effective than using the urea breath test. Using a less efficacious but cheaper eradication regimen is as cost-effective but with fewer deaths prevented. The cost-effectiveness is sensitive to the H. pylori prevalence, lag time, relative risk of gastric canvcer and complicated peptic ulcer disease, cohort estimate for future incidence of gastric cancer, and compliance. Moreover, cost/LYS rises to over £20,000 if there is a high level of opportunistic eradication of H. pylori in patients presenting with dyspepsia and a reduced efficacy of eradication on gastric cancer risk.
The benefits of screening take time to accrue and are very sensitive to the discount rate. At 6% rates the cost-effectiveness does not fall below £20,000 for 30 years.
Population screening for H. pylori is likely to be cost-effective with a cost/LYS of under £10,000 for the base assumptions, which compares favourably with other screening programmes. However the benefits take time to accrue and this cost/LYS is over an 80-year follow-up. Once-only screening at age 40 with a prevalent round for people aged 40–49 appears to be the most pragmatic policy. A major uncertainty is the effect of eradication of H. pylori on gastric cancer risk. The cost-effectiveness of H. pylori screening would be reduced if there were extensive H. pylori opportunistic testing of all dyspeptic individuals presenting to primary care
Implications for further research:
Key issues that could be addressed include:
1) The association between H. pylori, non-steroidal anti-inflammatory drugs (NSAIDs) and complicated peptic ulcer disease, in order to derive the independent relative risk of compli¬cated ulcer in H. pylori-positive individuals compared with those who are H. pylori-negative. Case–control studies are needed; these could be undertaken relatively quickly.
2) The efficacy of eradication of H. pylori on pre-cancerous pathological changes; the results of current trials concerning gastric metaplasia are awaited.
3) The cost-effectiveness of a ‘test and treat’ policy for peptic ulcer disease , and the impact of such a policy on opportunistic screening.
4) The model could be used to re-evaluate the cost-effectiveness of H. pylori screening in the light of updated data on the key parameters. If appropriate, a pilot H. pylori screening programme could be evaluated, probably screening all 40 to 49-year-olds as a prevalent round and then all individuals as they reach the age of 40. This would provide information on compliance, eradication and reinfection (in a sample), the impact on peptic ulcer disease and gastric pathology, and the impact of opportunistic testing in the non-screened group.
5) The model could be used to evaluate the effects of screening in other populations.
|Item Type:||Monograph (Project Report)|
|Additional Information:||2006 Impact Factor for Health Technology Assessments is 5.29|
|Keywords:||cancers, digestive diseases, cancer of stomach, peptic ulcers, primary care|
|Subjects:||R Medicine > RC Internal medicine > RC0254 Neoplasms. Tumors. Oncology (including Cancer)
R Medicine > RA Public aspects of medicine > RA0421 Public health. Hygiene. Preventive Medicine
H Social Sciences > HJ Public Finance
|Divisions:||University Structure - Pre August 2011 > School of Medicine > Cancer Sciences
|Date Deposited:||20 Jul 2007|
|Last Modified:||27 Mar 2014 18:30|
|Publisher:||National Coordinating Centre for Health Technology Assessments|
|RDF:||RDF+N-Triples, RDF+N3, RDF+XML, Browse.|
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