Who MPN CVD 2002.01
Who MPN CVD 2002.01
Who MPN CVD 2002.01
N D
in L- M-I C
through C-B & H S
C
S S
Background
Objectives of the meeting
e Wellcome Trust
e World Health Organization
S P M I S
. Agreement of remit
. General strategies for the medical management of secondary prevention
. Drug options for use in the secondary prevention of cardiovascular disease
. Lifestyle changes
. Health system research
. Different country settings
R I S P
I H S D C
. Secondary prevention as a key component of public health strategy
. Assessment of the current status of secondary prevention of major s
. Initiatives for scaling up secondary prevention in countries
. Health services
. Essential drugs
. Guidelines
. Patient education programmes
. National and regional policies
. Partnerships
. Combination therapy
WORKING PAPER: S P N D
T C- H S I
L P
/
S S
S P
M I S
Agreement of remit
Current evidence of cost-effective interventions
for secondary prevention of myocardial infarction and stroke was presented and discussed.
A series of overviews and perspectives were
given about the problems and experiences encountered in various developing countries. A
general discussion accepted the proposition that
the focus of treatment should be on proven costeffective interventions (medication and making
changes to lifestyles). Such interventions should
be considered when individuals seek treatment
from the health care system for such as a
myocardial infarction, an ischaemic cerebral
episode or stroke, or if they have developed
angina or peripheral vascular disease. Since
diabetes carries a substantive risk, middle-aged
patients with diabetes should also be classified
as at high risk of a episode.
Lifestyle changes that have a major impact on secondary prevention of major CVDs:
Smoking
cessation
Healthy diet
Weight
control
Regular moderate physical activity
of lives saved per year. Aspirin is exception- tive proportion of ischaemic to haemorrhagic
ally cheap and effective so the implementation
stroke patients is unclear and in many health
of lifestyle changes (avoidance of smoking,
systems clinical differentiation for therapeutic
dietary changes, weight control and physical
purposes is not possible. In the light of this, the
activity) plus the routine daily use of aspirin
combination of a diuretic and an should
are within the reach of the
be considered a routine oppoorest societies. Smoking
tion for the treatment of
Daily use of low-dose
cessation and other lifestyle
hypertension in all patients
aspirin reduces the risk
changes can be promoted
who have had a cerebral
on a societal level as part of
episode, regardless of their
of stroke and myocardial
general health promotion,
blood pressure values. In a
infarction or vascular
and smoking cessation and
recent study, the benefits of
death by one quarter
aspirin use should be clearly
blood pressure reduction in
set out as a minimum repatients with a cerebral vasquirement for the support of patients by
cular episode was evident in terms of reduced
the Health Services.
strokes and total death rates throughout the
blood pressure range. ese findings, if further
substantiated by clinical trials, will open up the
The evidence clearly shows that the follow- possibility for developing community-based
ing categories of drugs are of proven efficacy:
projects, or possibly even of selling antihyperbeta-blockers, angiotensin converting enzyme
tensives over-the-counter without the need for
inhibitors (), statins, and thiazide diuretics.
routine blood pressure monitoring. e thiazide
It has been shown that if these drugs are made
diruetic, bendrofluazide, is as cheap as aspirin
available in a generic, non-patented form, many
and generic s are now also cheap. Statins are
patients in middle-income countries can probalso increasingly recognized as being effective in
ably afford most, if not all, of them. e cost
reducing stroke rates, regardless of the type of
of statins will shortly come down as the patent
stroke. Furthermore, given their proven value in
on lovastatin expired in late . Furthermore,
other s, countries should now consider the
as each category of drugs listed above operates
additional use of a statin particularly in patients
through different pharmacological mechanisms,
with elevated serum cholesterol.
their combined use is of great potential value
to many categories of patient.
Drug costs
Statins
Thiazide
Angiotensin
diuretics
Combination therapy
controlled trials. e inexpensive s currently available are known to have side effects in a
small proportion of patients e.g. cough ()
and dizziness with hypotension (<).
e) Study of the interactions and effects of a
combination of drugs on physiological mechanisms.
f ) Studies on adherence to treatment.
It was accepted that the rationale for this approach had to be set out in detail before it
could be recommended to national professional
groups and ministries. W has produced a
useful preliminary overview of this approach.
e use of multiple drugs might be more acceptable if they were to be combined into a single
pill containing all four categories of drugs, for
example, aspirin, a beta-blocker, an inhibitor and a statin, and taken once a day. e use
Lifestyle changes
of a single pill could well encourage patients to
adhere to treatment as well as seriously reduce
e focus on drug therapy for secondary prethe cost of the drugs.
vention must not detract from the role of other
With the exception of patients suffering from
interventions. Smoking cessation has a greater
peripheral vascular disease who do not respond
impact than any single drug even when the drug
well to beta-blockers, the use of a combina- is administered appropriately. On a national
tion (fixed-dose) pill could be considered and
level it was clearly recognized that promoting
evaluated in patients suffering
health measures, for example
from all other cardiovascular
encouraging dietary change
Smoking cessation has a
conditions. It could be argued
and physical activity, could
greater impact than any
that there would be little
be of great importance.
single drug even when
need for monitoring except
While some participants in
of compliance with the drug
the meeting felt programmes
the drug is administered
regimen however, this would
to encourage smoking cessaappropriately
require careful evaluation
tion and dietary and physical
within different societies.
activity programmes should
Such an evaluation could take five years or
be an integral part of secondary prevention
more to complete and would require careful
protocols, others felt that the impact of these
assessment of the following:
additional measures, while very worthwhile,
a) Stability testing.
were either time-consuming or without the
b) Bio-availability testing.
strength of evidence available for drug interc) Assessment of the short-term effects of the
ventions. ese differences notwithstanding, it
drugs on blood pressure, low density lipopro- was nonetheless agreed that the development
tein cholesterol and platelet aggregation, to
of a strategy using a combination of pharmaensure that the effects of the fixed-dose pill are
cological and non-pharmacological approaches
similar to those obtained by the use of each in- would be valuable.
dividual drug, and that the effects are the same
It is important to be aware that clinical trials
in developing country populations as those seen
such as those used to test drugs are not always
when the drugs were tested extensively in high- possible when attempting to evaluate the imrisk Caucasian populations.
pact of lifestyle changes such as dietary changes,
d) Assessment of safety and short-term symptoincreasing physical activity and weight control.
matic side effects. is need is well recognized
It is therefore necessary to draw on available
and greater rigour can be applied to such an
evidence from other sources, in particular, longassessment if it is conducted as part of placebo
term prospective cohort studies.
/
R
I S P I H
S D C
Projects should be initiated, in selected developing countries with diverse health care systems,
to assess the secondary prevention systems
currently operating within certain countries.
As part of these projects, the following items
should be assessed:
a) estimated numbers of persons who require
secondary prevention treatment (present;
projected for and ) disaggregated by
age, gender and socioeconomic status. Such estimates should identify the number of persons
diagnosed with or diabetes, the proportion of such persons who have been prescribed
treatment that has been found to be effective
for secondary prevention, and the proportion
/
Health services
Essential drugs
All five classes of drugs, whose efficacy as lifesaving interventions is based on strong clinical
trial evidence, should be included in the list
of essential drugs which should be available in
primary health care at low cost.
ese are:
Aspirin
Beta-blockers (prototype drugs: atenolol,
metoprolol)
Thiazide diuretics (prototype drugs: hydrocholorothiazide, chlorthalidone)
(prototype drugs: enalapril, ramipril )
Statins (prototype drugs: lovastatin, simvastatin).
is will require the inclusion of statins in the
list of essential drugs recommended by
and altering the prototype drugs currently
identified in the list.
Action: WHO
Guidelines
Based on a local appraisal of resources the guidelines should set out a modular programme of
secondary prevention that begins with highly
effective low-cost interventions such as smoking cessation and other lifestyle changes plus
/
National and regional policies should be developed in order to enable greater access to secondary prevention by all individuals identified
as being at high risk of major cardiovascular
events, including:
a) information on secondary prevention of
cardiovascular events
b) access to evidence-based treatment for addicted smokers (non-pharmacological and
pharmacological)
c) access to natural and processed foods which
provide nutrition-based cardiovascular protection
d) access to community-based facilities for
promoting regular moderate physical activity
e) access to essential drugs effective in secondary
prevention.
Partnerships
should intensify its interaction with governments, the pharmaceutical industry and the
World Trade Organisation Organization ()
to improve access to essential drugs and to
develop mechanisms that will promote the production and supply of these drugs (identified
in Recommendation ) and reduce their cost,
so as to ensure that they are both available and
affordable in low- and middle-income countries.
Secondary prevention of should be placed
high on the agenda of discussions on essential
drugs that has initiated with the as
well as with the pharmaceutical industry.
Action: WHO, World Trade Organization,
pharmaceutical industry
10
Combination therapy
-
A working paper for the Wellcome Trust Meeting on
Secondary Prevention, Cambridge, August *
* Prepared by Drs S. Mendis, A. Alwan and A. Mandil,
Management of Noncommunicable Diseases Department, .
Comments and critical input from Drs R. Beaglehole, R. Collins, C. Davies, D. Maclean,
R. Peto, G. Shaper, A. Weilgoz, S. Yusuf & D. Yach are gratefully acknowledged.
1. Background
In , noncommunicable diseases (s) were
responsible for approximately of deaths in
the world, and for of the global burden of
disease. Based on current trends, by the year
these diseases are expected to account for
of deaths and of the burden of disease
(). A substantial portion of this mortality and
burden of disease can be attributed to cardiovascular diseases (), cancer, chronic respiratory
conditions and diabetes. In , alone was
responsible for approximately half of all
deaths and one fourth of the global burden of
disease (). , cancer, chronic respiratory disease and diabetes are the diseases that are being
targeted by the Global Strategy for
Prevention and Control, adopted at the General
Assembly of the World Health Organization in
May ().
In , s were responsible for of
total mortality and of the total burden of
disease in low- and middle-income countries.
Low- and middle-income countries also suffer
the major burden of the epidemic. In ,
two-thirds of global deaths and three quar /
Patients with established coronary heart disease or cerebrovascular disease are at the highest
risk for subsequent coronary and cerebral events.
Survivors of myocardial infarction () are at
increased risk of recurrent infarctions and have
an annual death rate of at least five to six times
that of people of the same age who do not have
coronary heart disease (). Similarly, patients
who have suffered a stroke are at an increased
risk of a further stroke, about per annum
(), and are very likely to experience coronary
heart disease. ere is considerable scientific
evidence to show that specific interventions
can reduce the risk of further vascular events
in patients with and type- diabetes.
Despite known substantial benefits and
generally low treatment costs, it has been reported that appropriate measures for secondary
prevention after have been implemented in
less than half of eligible patients, even in highincome countries (,). Because of inequitable
and inaccessible health care systems, inefficient
use of limited resources and the investment of
already scarce resources in interventions that
are not cost-effective, the availability of secondary prevention for is likely to be far
scarcer in low- and middle-income countries.
Patients with established coronary heart disease
and cerebrovascular disease experience recurrent morbid events such as stroke, myocardial
infarction and heart failure that are costly to
treat. However, they also provide the greatest
potential for cost savings, through the use of
cost-effective interventions (). e results
of cost-effectiveness analyses of secondary
prevention measures indicate that secondary
prevention measures for are highly costeffective when compared with many other
routine medical interventions (,).
the latter are: aspirin, beta-blockers, angiotensin converting enzyme inhibitors (),
lipid lowering drugs and antihypertensives.
Strong evidence for the efficacy of these drugs
has been obtained from Randomized Clinical
Trials (s), which have mostly taken place
in affluent societies (). Unfortunately
little evidence, if any, has come from studies
conducted in low- and middle-income countries. us, many of the recommended medical
interventions are based on s carried out in
developed countries and may cause economic
hardship when applied in developing nations.
Selected scientific evidence found in recent literature on cost-effective secondary prevention
interventions for cardiovascular and cerebrovascular disorders is cited below. Evidence for
pharmacological interventions is presented first
(), followed by that for behavioural risk
factor modification ().
..
4.1.1 Aspirin in secondary prevention of CVD
e benefits of aspirin in the secondary prevention of myocardial infarction are well
established and documented. In patients
who had myocardial infarction, reviewed by the
Antiplatelet Trialists, low to medium doses of
aspirin ( mg/day) led to a reduction
in death, a reduction in re-infarction and a
reduction in non-fatal stroke (). Available
evidence suggests that there are no added benefits from using daily doses higher than mg.
Currently, there is no clear evidence to suggest
that any other anti-platelet regimen is more effective than aspirin.
One systematic review that compared antiplatelet treatment to a placebo suggested that at
months, people would need to be treated
with aspirin rather than a placebo to prevent
one additional vascular event (). With regard
to cerebrovascular disease, s have found
that the routine use of prolonged antiplatelet
treatment (aspirin mg) is beneficial for the
prevention of vascular events in people with a
prior (presumed ischaemic) stroke or transient
ischaemic attack, unless there is a clear con-
that poorly controlled hypertension was associated with an increased risk of stroke. erefore,
achieving good blood pressure control in elderly
hypertensives receiving treatment has the potential of preventing stroke ().
e Perindopril Protection Against Recurrent
Stroke Study () has recently provided
evidence of the benefits of lowering blood pressure on the risk of stroke recurrence among
patients with a history of cerbrovascular disease
in the previous years (). In this study,
patients were randomized to receive perindopril
alone, perindopril plus indapamide, or placebo.
e risk reduction in the perindopril group and
combination group compared to placebo were
and respectively.
As far as the prevention of vascular complications in diabetics is concerned, the United
Kingdom Prospective Diabetes Study ()
has shown that in patients with type- diabetes,
the risk of diabetic complications is strongly
associated with raised blood pressure (). Any
reduction in blood pressure is likely to reduce
the risk of complications, with the lowest risk
being in those with a systolic blood pressure of
less than mm Hg.
There are many drugs available for the
pharmacological management of hypertension. However, comparisons of different
anti-hypertensives have shown that newer and
more expensive drugs are not more effective
than thiazides, diuretics and beta-blockers in
reducing outcomes ().
.
In addition to pharmacological interventions
for secondary prevention, evidence suggests
that modification of risk factors through
smoking cessation, and encouraging a healthy
diet and physical exercise can also significantly
contribute to a reduction in cardiovascular mortality in people with established ().
4.3.1 Smoking control
Smoking is associated with approximately
twice the rate of mortality from and an
even higher risk for cancer (). Evidence from
epidemiological studies indicates that people
with coronary heart disease who stop smoking
rapidly reduce their risk of recurrent coronary
events or death (). Angina patients who
smoke have a greater risk of later infarction or
death than do those who do not smoke. After
coronary surgery reinfarction as well as new infarctions and angina pectoris are less common
among patients who stop smoking than they are
among those who continue to smoke ().
Results of a meta-analysis of cohort studies
suggest that smoking cessation after myocardial
infarction is associated with a reduction
in mortality (). e number needed to quit
smoking to save one life is assuming a mortality rate of in continuing smokers. Smoking
has also been shown to be a powerful predictor of recurrent heart failure and myocardial
infarction as well as mortality in patients with
left ventricular dysfunction. Quitting smoking
appears to have a substantial and early effect
(within two years) on decreasing morbidity and
mortality in this patient group. e benefits
of stopping smoking are therefore at least as
important as those to be gained from recommended drug treatments in patients with left
ventricular dysfunction ().
the effects of physical activity, a recent systematic review has summarized the large amount
of evidence obtained from prospective cohort
studies (). ese studies demonstrate that
physical inactivity is a major risk factor for
and that changing levels of activity can improve
health outcomes, even in the elderly.
9. Approach
. :
During this phase, an essential package of
evidence-based, cost-effective interventions
for secondary prevention of (coronary
heart disease and stroke) will be identified.
A general protocol for a multi-country pilot
project that integrates secondary prevention
into community-based primary prevention
programmes will be developed. Organizational
models for implementing the protocol with
particular reference to primary care will be
proposed. Individual studies will be designed
by local principal investigators in response to
country/region-specific circumstances, with the
collaboration and advice of other international
scientists where appropriate.
Proposed activities:
. Establish a Steering Committee, including
staff/external experts, for planning, quality assurance and monitoring purposes.
. Organize a consultation with international
experts and potential investigators from developing countries to discuss the following
issues:
(i) To identify cost-effective interventions for
the secondary prevention of that can be
integrated into the health systems of developing
countries.
(ii) To identify mechanisms and tools to assess the feasibility of these interventions and
their impact on major risk factors and selected
cardiovascular outcomes.
(iii) To develop a plan of action for the
development of a general protocol for community projects on evidence-based, cost-effective
interventions aimed at controlling the major
risk factors and reducing cardiovascular
outcomes.
(iv) To discuss strategies for integrating
secondary prevention into the existing health
care infrastructure and build national capacity
to meet health services needs for the secondary
prevention of the major s.
. Develop the protocol for the pilot project
which identifies the target population, methodology, indicators for evaluation and defines
organizational models for implementation.
. Identify the basic requirements of the health
system for incorporating the selected interventions into primary health care (e.g. training,
logistics, referral system and other relevant
components). Issues that need to be considered
include the cost of relevant drugs in different
countries, other direct and indirect costs, implications for the health system, and the role of
the various levels of health professionals.
. :
(i) Pilot testing will be carried out in selected
countries from the Regions.
(ii) Identify countries and potential local investigators, adapt the protocol developed in phase
and train local teams.
(iii) Implement the basic changes required in
the infrastructure of the existing health system
in the pilot areas.
. :
(i) Implement pilot projects.
(ii) Monitor process and outcomes.
. :
Evaluate the process of the programme, the
short-term impact of the interventions, and
the suitability of the programme to serve as a
demonstration project for the establishment of
other national programmes.
11. References
. World Health Organization. Global Strategy for
the Prevention and Control of Noncommunicable
Diseases. Report by the Director General. /.
Fifty-ird World Health Assembly, May .
. World Health Organization. World Health
Report . Geneva: , .
. van der Sande MAB, Bailey R, Faal H, Banya
WA, Dolin P, Nyan OA, Ceesay SM, Walraven GE,
Johnson GJ, McAdam KP. Nationwide prevalence
study of hypertension and related non-communicable diseases in e Gambia. Trop Med Int Health,
, ():.
. Forrester T, Cooper RS, Weatherall D.
Emergence of Western diseases in the tropical world:
the experience with chronic cardiovascular diseases.
Br Med Bull, , ():.
. Pearson TA. Cardiovascular disease in developing countries: myths, realities, and opportunities.
Cardiovasc Drugs er, , ():.
. Marmot MG, Davey Smith G, Stansfeld S et al.
Health inequalities among British civil servants: the
Whitehall II Study. Lancet, , ():.
. Marmot MG, Shipley MG, Rose G. Inequalities
in death specific explanation or a general pattern?
Lancet, , ():.
. Manson-Siddle CJ, Robinson MB. Super Profile
analysis of socio-economic variations in coronary
investigation and revascularisation rates. J Epidemiol
Community Health, , ():.
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L P
WHO/W T M E
S P
N D
L- M- C
C- H S I
H, C, UK
A
Professor Rory Collins
Harkness Building
Radcliffe Infirmary
Oxford, ox ,
+()
Fax: +()
Email: gale.mead@ctsu@ox.ac.uk
Professor Liming Li
Ministry of Health
Research Department
Tehran, Islamic Republic of Iran
+
Fax: +
Email: afzali@hbi.or.ir
Radcliffe Infirmary
Oxford, ,
+()
Fax: +()
Dr Curtis Meinert
Department of Cardiology
All India Institute
of Medical Sciences
Ansarinager
New Delhi , India
+
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Email: ksreddy@satyam.net.in
Dr Hector Moguilevsky
Ministerio de Salud
Avenue de Julio
Buenos Aires , Argentina
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Email: moguilev@satlink.com
Professor V. Mohan
Madras Diabetes
Research Foundation
Conran Smith Road
Gopalapuram
Chennai , India
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Fax: +
Email: mvdsc@vsnl.com
Dr K.T. Shenoy
Dr Chaisri Supornsilaphachai
Social & Behavioural Medicine
Division
Department of Medical Services
Ministry of Public Health
Tivanond Road
Amphur Muang
Nonthaburi , ailand
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Email: chaisri@health.moph.go.th
Dr Krisela Steyn
Dr K.R. ankappan
Dr Salim Yusuf
(by Conference line)
Barton St. E
McMaster Clinic, Room
Hamilton General Hospital
Hamilton, Ontario ,
Canada
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Fax: +
Email: yusufs@mcmaster.ca
T W T
Miss Sam Balakrishnan
Euston Road
London, ,
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Email: s.balakrishnan@wellcome.ac.uk
Dr Catherine Davies
Euston Road
London, ,
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Email: c.davies@wellcome.ac.uk
Dr Wendy Ewart
Euston Road
London, ,
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Email: w.ewart@wellcome.ac.uk
Euston Road
London, ,
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Email: mhoney@wellcome.ac.uk
Dr Richard Lane
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Dr Ala Alwan
Avenue Appia
Geneva , Switzerland
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Dr Raphael Bengoa
Avenue Appia
Geneva , Switzerland
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Dr Shanthi Mendis
Avenue Appia
Geneva , Switzerland
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Dr Pekka Puska
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Geneva , Switzerland
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Euston Road
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Email: r.lane@wellcome.ac.uk
Dr Jacob Sweiry
Euston Road
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