Jump to: Page Content, Site Navigation, Site Search,
You are seeing this message because your web browser does not support basic web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.
Tom Marshall Public Health and
Epidemiology, University of Birmingham, Birmingham B15 2TT Correspondence to: T
Marshall T.P.Marshall{at}bham.ac.uk
| |
Abstract |
|---|
|
|
|---|
Objective:
To develop a model to determine the
resource costs and health benefits of implementing guidelines for the
prevention of cardiovascular disease in primary care.
Design:
Modelling of data from six strategies for prevention of cardiovascular disease. Strategies incorporated two ways
of identifying patients for assessment: traditional (assessment of all
adults) and novel (preselection of patients for assessment using a
prior estimate of their risk of cardiovascular disease). Three
treatment strategies were modelled in conjunction with each identification strategy.
Setting:
England.
Subjects:
Patients aged 30 to 74 eligible for primary prevention strategies for cardiovascular disease who were selected from
a hypothetical population of 2000.
Main outcome measures:
Resource costs of assessing
eligible adults, providing treatment and follow up and number of
cardiovascular events this should prevent.
Results:
Novel strategies prevented more
cardiovascular disease, at lower cost, than traditional strategies.
Some treatment strategies prevent more cardiovascular disease with
fewer resources than others. The findings were robust across a range of
different assumptions about workload.
Conclusion:
Preselecting patients for assessment
makes better use of staff time than assessing all adults. Treating many patients with low cost drugs is more efficient than prescribing a few
patients intensive antihypertensives and statins. Authors of guidelines
should model workload implications and health benefits of following
their recommendations.
|
What is already known on this topic
There are data on the distribution of cardiovascular risk factors in the population What this study adds
Strategies that prioritise patients for risk assessment may reduce staff time to the extent that more patients can be treated and more disease prevented within available resources Statins and angiotensin converting enzyme inhibitors cost more than identifying and treating new patients, so strategies avoiding these may allow more disease to be prevented within available resources |
| |
Introduction |
|---|
|
|
|---|
The UK government policy framework endorses joint British
recommendations on preventing coronary heart disease: primary care teams must assess patients' risk of cardiovascular disease every five
years and treat eligible patients (see box on bmj.com).1 The recommendations require many hours of clinical staff time and
considerable cost. Part of this commitment will be devoted to assessing
patients who ultimately do not need treatment. The recommendations do
not quantify the resource implications or the health benefits of this
policy. We describe a model for estimating the efficiency (total health
service resources invested versus cardiovascular events prevented) of
six strategies for primary care based prevention of cardiovascular disease.
| |
Methods |
|---|
|
|
|---|
The joint British recommendations require patients to undergo five yearly assessments for risk of cardiovascular disease. Therefore our model analysed resource implications and health benefits over a five year period. Resource implications were considered from the perspective of the health service. The data for our model came from several sources (see bmj.com).
Cardiovascular risk estimation
We used the Framingham coronary heart disease risk equation
and the cerebrovascular disease risk equation to estimate the number of
coronary events prevented and the number of strokes
prevented.2 The combined Framingham risk equation predicts
the risk of all cardiovascular events (stroke, coronary event,
peripheral vascular disease, or heart failure). We used it to calculate
prior risk estimates for the preselection strategies.
Distribution of risk factors and risk
Using data from the 1998 health survey of England, we
estimated the distribution of systolic blood pressure and cholesterol
concentration by age, sex, history of diabetes, and smoking history in
individuals who neither had prior cardiovascular disease nor were
receiving antihypertensives.3 Then we generated a
hypothetical population whose distribution for age, sex, and risk
factors reflected a typical general practitioner list. Our typical
general practitioner list had 939 patients, aged between 30 and 74, eligible for primary prevention services.
Prevention strategies modelled
The joint British recommendations do not indicate how to
prioritise assessed patients for treatment. In strategies JBR-1 (joint
British recommendations-1), JBR-2, and JBR-3 all patients undergo five
yearly assessments for clinical risk. Once assessed the general
practitioner treats them in rank order of their risk of coronary heart
disease: the total number of patients treated being determined by the
total resources available.
In strategies RM-1 (Rouse Marshall-1), RM-2, and RM-3 a two stage
assessment is proposed (see box and bmj.com).
|
Cardiovascular disease prevention strategies
modelled
Identification and prioritisation Strategies JBR-1, JBR-2, and JBR-3
Strategies RM-1, RM-2, and RM-3
Treatment All strategies:
|
| |
Resource implications |
|---|
|
|
|---|
We assumed that all clinical tasks are carried out by practice
nurses. The total health service cost of providing an hour of practice
nurse clinic time is £28 ($43;
44).4 Costs of blood
tests were derived from the Pathology Services costings.5 Drug costs were obtained from the British National
Formulary.6 Dispensing costs were calculated at 87.4p
for each prescribed item on the assumption that four prescriptions are
issued each year.7 Where appropriate, costs have been
discounted at 6% a year. We estimated that each risk assessment takes
a minimum of 20 minutes of clinical staff time.
Treatment and follow up
Ongoing management of patients receiving treatment requires at
least two follow up clinic appointments a year, totalling 20 minutes of
clinical staff time.1 Patients receiving thiazide diuretics require an annual estimation of electrolyte and uric acid,
and patients receiving statins require annual liver function tests.
| |
Health benefits |
|---|
|
|
|---|
We calculated the benefits of treatment as the number of
cardiovascular events prevented. As patients may have two
cardiovascular events, this differs from the number of patients having
a cardiovascular event. For each patient, the absolute risk reduction
is the product of the initial risk and the risk reduction with
treatment. The assumed risk reductions afforded by treatment are given
on bmj.com.
| |
Results |
|---|
|
|
|---|
Cost effectiveness
Technical efficiency: maximising benefits within
total resources
For any given allocation of resources to the primary
prevention of cardiovascular disease, more cardiovascular events can be
prevented under RM strategies than under the equivalent JBR strategies.
A primary care team can prevent 13.5 events for £49 960 under
strategy RM-2 or 13.5 events for £15 110 under RM-3. The most
efficient strategy for a primary care team with this budget is
therefore RM-3. A primary care team can prevent 16.7 events for
£119 806 under strategy RM-1 or 13.5 events for £73 716 under RM-2.
The most efficient strategy for a primary care team with this budget is
therefore RM-2. For a primary care team with over £119 806 the most
efficient strategy is RM-1. Figure 1 shows the maximum number of
events prevented with increasing amounts of resources under each
strategy.
|
Maximising efficiency within available clinical staff time
For practices allocating one, two, or three clinics a month
to the primary prevention of cardiovascular disease, RM strategies
dominate JBR strategies (fig 2). At one clinic a month there is not
sufficient clinical time to assess all eligible adults, JBR strategies
therefore cannot be implemented. Strategy RM-3 prevented 9.1 cardiovascular events at a cost of £863 for each event prevented. RM-2
prevented 1.9 more events at an incremental cost of £10 518 for each
event prevented. RM-1 prevented 4.6 more events than RM-2 at an
incremental cost of £17 808 for each event prevented.
|
Sensitivity analysis
Selecting only patients over 50 for primary prevention and
altering assumptions about workload did not influence the results of
our model. Nor did prior knowledge of patients' blood pressures: RM
strategies prevent more cardiovascular disease than JBR strategies.
Varying the cost of prescribing statins or angiotensin converting
enzyme inhibitors altered our findings only if they cost under £231
for five years' treatment.
| |
Discussion |
|---|
|
|
|---|
We assumed that all eligible patients accepted and complied fully with treatment. In reality some decline assessment, and some do not comply with prescribed treatment. Reducing the rest period before measurement of blood pressure to under four minutes risks significant overestimation.8 Blood tests take longer than 2.5 minutes and, given the variability of cholesterol concentrations, accurate estimation takes more than two measurements.9 Calculating the risks of cardiovascular disease and counselling patients probably takes longer than 20 minutes. Follow up may also cost more than we estimated. Patients often visit their general practitioner more frequently than twice yearly, and further investigations may be needed. The cost of staff time may be underestimated, since medical time costs more than nursing time.
Our model assumed no patients leave or join the practice over five years. An annual turnover of 10% in the practice population increases the number of five yearly assessments by 41%. In contrast, periodically recalculating prior risk estimates and re-ranking patients takes only minutes, and the primary care team could fill clinic time left by patient departures by inviting the next highest ranked patients for assessment. The turnover of practice populations therefore strongly favours the RM strategies.
Our model assumed that primary care teams following the joint British recommendations do prioritise patients for treatment on the basis of their risk of coronary heart disease. In fact, patients whose risks are above a threshold are likely to be treated as they are identified. Our model therefore exaggerates the effectiveness of the joint British recommendations. The RM strategies make no such assumption.
Our model used the lowest cost drug for each category of treatment. Non-generic enalapril costs twice as much as generic enalapril. Simvastatin was costed at 10 mg a day, whereas higher doses are usual.10 Compared with clinical practice, our model therefore exaggerated the cost effectiveness of strategies using simvastatin and enalapril. Finally, we probably exaggerated the benefits of intensive blood pressure lowering.
Implications of model for treatment
Our model raises questions about current treatment recommendations in the context of a population based programme for the
prevention of cardiovascular disease. Recent research confirms statins
are effective irrespective of initial cholesterol concentrations,
across a wide range of risks.11 Our model showed that they
are not cost effective even for patients meeting current criteria. More
intensive blood pressure lowering may reduce risk but does not justify
the additional cost. This casts doubt on the importance of achieving
blood pressure targets in a publicly financed, population based
programme for the prevention of cardiovascular disease. Aspirin is
currently recommended only for patients whose risk of coronary heart
disease over five years exceeds 15%.1 Our model suggests
it may be cost effective for patients at much lower risk levels.
Conclusions
We recommend that authors of future guidelines should make
explicit statements about the resource implications, health benefits,
and efficiency of implementation strategies. Furthermore, the
efficiency of prevention of cardiovascular disease in primary care
could be greatly enhanced by two innovations: prioritising patients for
assessment on the basis of a prior estimate of their cardiovascular
risk and avoiding costly drugs such as simvastatin and enalapril.
| |
Acknowledgments |
|---|
Contributors: See bmj.com
| |
Footnotes |
|---|
Funding: None.
Competing interests: None declared.
The full version of this article
appears on bmj.com
| |
References |
|---|
|
|
|---|
| 1. | Wood D, Durrington P, Poulter N, McInnes G, Rees A, Wray R on behalf of the societies. Joint British recommendations on prevention of coronary heart disease in clinical practice. Heart 1998;80:(suppl 2). |
| 2. |
Wolf PA, D'Agostino RB, Belanger AJ, Kannel WB.
Probability of stroke: a risk profile from the Framingham study.
Stroke
1991;
22:
312-318 |
| 3. | Department of Health. Health survey for England '98. London: Stationery Office, 2000. |
| 4. | Netten A, Curtil L. Unit costs of health and social care 2000. University of Kent at Canterbury: Personal Social Services Research Unit, 2000. |
| 5. | London School of Hygiene and Tropical Medicine. Local standard costs of pathology services. Compiled by Rheinhold Gruen (unpublished data). |
| 6. | British Medical Association, Royal Pharmaceutical Society of Great Britain. British national formulary. London: BMA, RPS, 2000 (No 41.) |
| 7. | Compiled on behalf of the Department of Health by the Prescription Pricing Authority. Drug tariff Jan 2002. London: Stationery Office. |
| 8. | Bakx JC, Netea RT, van den Hoogen HJM, Oerlemans G, van Dijk R, van den Bosch WJHM, et al. The influence of a rest period on blood pressure measurement. Huisarts Wetenschap 1999; 42: 53-56. (In Dutch.) |
| 9. |
Marcovina SM, Gaur VP, Albers JJ.
Biological variability of cholesterol, triglyceride, low- and high-density lipoprotein cholesterol, lipoprotein(a), and apolipoproteins A-I and B.
Clin Chem
1994;
40:
574-578 |
| 10. |
Pedersen TR, Kjekshus J, Berg K, Olsson AG, Wilhelmsen L, Wedel H, et al.
Cholesterol lowering and the use of healthcare resources: results of the Scandinavian simvastatin survival study.
Circulation
1996;
93:
1796-1802 |
| 11. | Medical Research Council and British Heart Foundation Heart
Protection Study. http://www.ctsu.ox.ac.uk/![]() |
(Accepted 4 April 2002)
Read all Rapid Responses