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PHARMAC and cardiovascular health in New
Zealand
The recent analysis by Stewart
et al1 again demonstrates how socioeconomic
factors are important determinants of health
outcomes.2 The additional comparison between
New Zealanders and Australians in the LIPID study is interesting, in that from
the data available no single point of difference can be identified. It is
unfortunate that the study design did not identify ethnicity, as it is well
recognised that Māori and Pacific people (even in higher socioeconomic
groups) do not fare as well as New Zealand
Europeans.3–6
It was therefore disappointing
to see that the accompanying editorial (Ellis and
Hamer)7 focused at least in part on a criticism
of PHARMAC’s historical stance on the prescribing of statins. These
criticisms have been answered on a number of occasions in the
Journal,8–11 and these responses
should be read as part of the debate.
Ellis et al use relative
international pharmaceutical expenditure figures to argue that New Zealand
spends too little on medicines. In fact this is a meaningless statistic, as the
price of medicines varies enormously between countries and depends on their
negotiating ability. They then congratulate PHARMAC for containing costs and
insisting12 on best value for money.
The usage of statins in New
Zealand was closely monitored between 1993 to 2002 using Special Authority
approvals data. During that time, access was progressively widened; however at
no time did we achieve a greater than 40% uptake for the targeted groups (20% at
the time of the LIPID study). We have calculated the loss of life from
non-uptake in eligible patients was 26% higher than that from road traffic
crashes over that time.* If we are going to improve our population health status
then the most fertile area is to ensure that those who are in need really do
access appropriate care. By comparison, the potency of statins is a relatively
minor issue.
Ellis
et al refer to unnecessary death and morbidity. The price of statins in 1996 was
so high that to treat everyone advocated by the 1996 NHF dyslipidaemia
guidelines would have cost some an extra $147 million each year for 137,000
patients; more than one-quarter of all community pharmaceutical spending at that
time. For context, this level of spending is much higher than the entire
cumulative year-by-year new investments PHARMAC has made over the last nine
years†—forgoing the health gains and costs savings to the rest of
the health sector from funding gabapentin for neuropathic pain, beta-interferon,
erythropoetin beta, atypical antipsychotics, venlafaxine, clopidogrel,
lamivudine, low-dose aspirin, alendronate, and imatinib, to name but a
few.
It should also be remembered
that the original evidence13 for the use of
statins was for secondary prevention, and good evidence for the benefits in
primary prevention is relatively recent. It is not appropriate to use
today’s evidence to judge yesterday’s standards.
Since
2003 there have been no restrictions on the use of simvastatin in New Zealand,
and our usage now outstrips
Australia9—where there are still
prescribing constraints (see graphs below).
We should remember that the
LIPID study data is now 10 to 18 years old, and it is now time to look forward
and address the problems. Our first priority should be addressing the equity
issues, and to that end PHARMAC has already initiated the One Heart Many
Lives campaign. This is a joint approach with DHBs and with close
cooperation from the National Heart Foundation. It focuses on Māori and
Pacific people and promotes general cardiac health, while at the same time using
statin usage as a surrogate measure of outcome.
Ellis and Hamer quite correctly
argue for greater clinical involvement in decision-making for heart disease. If
well done, real health gains and efficiencies could be made. However, if
clinicians do take a stronger role, they will also have to take responsibility
for the budget, not only for cardiac disease but also negotiate with other areas
of the Health Sector for a fair and equitable distribution—just like the
managers have to do now.
Peter Moodie
Medical Director PHARMAC Wellington Graphs:
![]() ![]() Sources: PHARMAC analysis of (1) NZHIS
PharmWarehouse dispensings and scripts data for statins, and (2) PBS services
data at http://www.medicareaustralia.gov.au/statistics/dyn_pbs/forms/pbs_tab1.shtml,
using PBS codes (http://www9.health.gov.au/pbs/scripts/search.cfm)
for atorvastatin, fluvastatin, pravastatin and simvastatin (codes 8213G, 8214H,
8215J, 8521L, 8023G, 8024H, 2833D, 2834E, 8197K, 2011W, 2012X, 8173E, 2013Y,
8313M, 2831B). Population denominators obtained from http://www.stats.govt.nz/ and http://www.abs.gov.au/
Footnotes:
*Historical burden of disease from statin non-uptake in
eligible patients, estimated from the gaps between estimated eligibility and
actual dispensings, i.e. the estimated numbers of non-uptaking eligible people,
and the consequent QALY losses from untreated cardiovascular disease (when
compared with statin treatment, according to the eligibility criteria in place
each month). Statin non-uptake over the 10-year period July 1991 to June 2001
meant that there were 6,930 ‘statistical deaths’ in New Zealand
through missed opportunities to gain QALYs, from 115,000 potential QALY gains
not realised. This number is 26% higher than the number of road deaths reported
to the LTSA during the same time period (5,499).
†Year-by-year between 1998/99 and 2006/07 PHARMAC
has invested $111 million for 173 new investments, for which $91 million for 65
investments initially benefitting some 286,000 patients are for medicines where
we can estimate health gains, saving some 6,460 QALYs, with $38 million nominal
savings elsewhere to the health sector (58% offsets) just in the initial 12
months of investments
References:
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