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Comparison of the content
of the New Zealand influenza pandemic plan with European pandemic plans
Nick Wilson, Michael G Baker
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Abstract
Aim To critically review version 16 of
the New Zealand (NZ) influenza pandemic plan in relation to the content of
European pandemic plans.
Methods We used a published framework
that had been developed for describing 29 European pandemic plans (all of which
were available in 2006). This framework was used to rate the content of the NZ
plan compared with the combined results for European plans.
Results In terms of plan content on
border control aspects, the NZ plan scored higher than the average European plan
(8.0 vs 4.9 out of 10.0 respectively) and similarly for the antiviral aspects
(13.5 vs 10.6 out of 17.0). However, it scored slightly lower for the vaccine
aspects (4.5 vs 5.3 out of 11.0). An alternate (more stringent) scoring system
suggested that the relative quality of the NZ plan was poorer for antiviral
aspects and fairly similar for vaccine aspects (to the average European plan).
Even so, this framework had various limitations and probably favoured European
countries which often have their own vaccine/antiviral production capacity. The
NZ plan may also have scored more highly if the framework used considered other
control measures (e.g. social distancing interventions). This comparison also
identified some gaps which could be worth addressing in the planned 2009 version
of the NZ plan (e.g. improved detail around priority groups for antivirals and
pandemic vaccine and consideration of pneumococcal vaccine).
Conclusions The NZ influenza pandemic
plan compared favourably with the average European plan in many aspects but not
all. There is scope for further improvements and additions to be made in the
next (2009) version of the NZ plan.
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The threat of pandemic influenza remains a substantial
concern globally. Recently the head of the World Health Organization (WHO) has
commented on this threat:
Turning to the threat of
pandemic influenza, [Margaret] Chan cautioned that ‘it has by no means
receded, and we would be very unwise to let our guard down or slacken our
preparedness measures.’ Countries with solid health infrastructures and
efficient mechanisms for reaching vulnerable populations will be in the best
position to cope, she said. 1
As well as being a concern for governments, survey data from
the United States indicates that “avian flu” is one of the three
biggest perceived health threats by the public (along with cancer and
HIV/AIDS).2
New Zealand (NZ) has responded to the pandemic influenza
threat by funding research,3 developing and
revising very detailed national level pandemic
plans,4 and running simulation exercises to
test and refine the planning tools.5 There has
also been active planning at the district health board
level.6 An earlier analysis of plans in the
Asia/Pacific region found the NZ national-level plan (version 14 in 2005)
“compared favourably with the best European
plans”.7
The current (version 16) NZ
plan,4 has been compared with other plans in
terms of its border control aspects and found to be comparatively well
developed.8 But there have been no other
published studies on this plan, despite the public health importance of such
work and the ongoing process of plan revision being undertaken in this country.
Methods
Framework—We used a published
framework that had been developed for describing the content of pandemic
plans.9 This work was also the data source for
the content information on the 29 European plans considered. Items in the
framework that were excluded are in Table 1. All these European plans were
eligible for inclusion if they were published before 30 September 2006 (which
was the same year that the current version 16 NZ plan was published).
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Item
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Reason for exclusion from this
analysis
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Restrictions anticipated on importing goods from affected
countries considered
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Most European countries referred to restrictions on
poultry imports with regard to this item. However this specific issue is not
relevant to NZ as live poultry imports are already illegal.
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Plans to secure pre-purchase agreement with vaccine
companies for the supply of pandemic strain vaccine
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This item was considered less definite than the
subsequent framework item which was focused on instead (i.e. if a secured
pre-purchase agreement had been made).
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Provisions to package active pharmaceutical ingredient in
capsule described
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This item was not considered relevant for NZ since the
antiviral stockpile is of fully made-up capsules.
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Country planning to stockpile antivirals
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This item was not considered relevant since NZ already
has a stockpile (instead the issue of the presence of a stockpile and its
documentation was focused on in the framework used).
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Antivirals planned for pre-exposure prophylaxis
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This item was considered too similar to the preceding
framework item which was focused on instead (i.e. “Antivirals planned for
pre-exposure prophylaxis during a pandemic”).
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Data abstraction and scoring—The
data extraction tool developed and used by the authors of the European plan
analysis9 could not be obtained from them.
Therefore for the 29 European countries the combined data were abstracted from
the three bar graphs in the published article.9
When compared with the numbers quoted in the text of this article, this
abstraction process appeared to be 100% accurate (i.e. the scale of the bar
graph was easily and accurately interpretable). The totals for all the countries
were averaged within each domain (see the bottom row of Tables 2 to 4).
Under each of the categories in the framework, the NZ
plan (including its associated appendices) was checked. This process involved a
full reading of the plan and then systematic word searches of all the files that
covered the full electronic version. A “yes” for content inclusion
was scored as a “1.0”. Where the NZ plan was not entirely explicit
in its coverage of a content area, this item was graded as “partly”
and was scored as “0.5”. In a more stringent alternative approach
the “partly” assessments were given a zero score.
Results
The NZ plan followed the general pattern of such plans
having elements of both a strategic plan and an operational plan (i.e. 25/29 of
the European plans had this pattern). In terms of page length, the NZ plan at
198 pages (with appendices) was the fourth longest. Longer plans were those from
Finland (202 pages), the Netherlands (59 pages plus 246 pages of appendices) and
Switzerland (249 pages in three parts).
In terms of plan content on border control aspects, the NZ
plan scored higher than the average European plan (8.0 vs 4.9 out of 10.0
respectively) (Table 2). Similarly, for the antiviral aspects (13.5 vs 10.6 out
of 17.0) (Table 4). However, the NZ plan scored slightly lower for the vaccine
aspects (4.5 vs 5.3 out of 11.0) (Table 3).
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Measures detailed in the plan
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For 29 European
countries (N)
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For
NZ*
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Comment with regard
to the NZ plan
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1.1) Absolute ban on the entry of people arriving from
affected areas.**
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5
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Yes (p139)
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Border closure from
affected areas is detailed in the NZ plan.
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1.2) Selective restrictions on the entry of people
arriving from affected areas.**
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16
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Yes (p139)
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This option exists in the
plan and may be combined with requiring time in quarantine for people from
certain pandemic-affected areas.
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1.3) Mentions following WHO recommendations on
travel
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16
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No
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The plan frequently refers
to WHO but not specifically to following WHO travel recommendations.
Nevertheless, the plan does detail the provision of advice to travellers (e.g.
p26).
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1.4) Information for travellers
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22
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Yes (p26)
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The plan provides examples
of travel advice health educational materials (p197).
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1.5) Measures at borders for international travellers
coming from or going to affected areas
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21
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Yes
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See below on exit screening
and entry screening.
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1.6) Entry screening anticipated.**
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17
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Yes (p44)
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The plan mentions
“intense surveillance” at the border and “enhanced
screening” by the Customs Service (p129). Nevertheless, there is no
specific mention of “health declarations” (for entry
screening).
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1.7) Exit screening anticipated
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10
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Yes (p141)
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The plan is quite detailed
on exit screening (i.e. health declarations and temperature measurements).
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1.8) Quarantine of passengers coming from suspected areas
anticipated.**
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11
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Yes (p134)
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This issue is detailed in
the plan. (Furthermore, local level planning for quarantine around international
airports has also been undertaken).
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1.9) Measures for travellers on board international
conveyances from affected areas
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9
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No
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There is no mention in the
plan of separation measures or provision of masks to passengers/crew. But the
plan does have detailed information about mask use in other settings.
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1.10) International cooperation with neighbouring
countries explicit
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14
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Yes (p26)
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The plan specifically
states such cooperation (especially with Australia) in many places.
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Total score (out of 10 categories)
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4.9/10.0
(average)
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8.0/
10.0
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* Example pages for the NZ
plan (i.e. in many cases there is additional detail in other parts of the
plan).
** This measure is not actually in WHO guidelines and
may even be advised against by WHO. Nevertheless, it was retained in the
framework as it might actually be appropriate in some circumstances and for
island nations which are likely to have better scope for successful border
control (see also the Discussion).
In a more stringent alternative approach (where the
“partly” assessments were given a zero score), the scores for
vaccine aspects dropped further behind the average for the European plans (i.e.
to 3.0 out of 11.0) (Table 3). For antiviral aspects the NZ plan score dropped
to only just above the average for the European plans (i.e. to 11.0 out of 17.0)
(Table 4).
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Measures detailed in the plan
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For 29 European
countries (N)
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For
NZ
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Comment with regard
to the NZ plan
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2.1) A strategic plan for pandemic vaccination
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28
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Yes (p99)
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The plan refers to
vaccination in many places and states the pandemic vaccine will be ordered at
the appropriate time (from an Australian manufacturer).
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2.2) A strategic plan for pneumococcal vaccination in
pandemic phase
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11
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No
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There is no mention of
pneumococcal vaccination in the plan.
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2.3) A strategic plan to vaccinate the whole
population
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18
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Partly (p169)
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This is not entirely clear
in the plan but it is probably implied by the statement: “until the
population at large is protected by vaccination”.
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2.4) Defined priority groups for influenza
vaccination
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26
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Partly
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The plan cross-refers to an
associated online document on ethical issues,10
which gives some statements that support prioritisation towards health
professionals and towards patients who would meet clinical criteria for
treatment (e.g. “influenza vaccination”) during normal times.
Appendix D of the plan also discusses issues around “reciprocity”
and “fairness” which may inform the prioritisation issue. See the
additional text in the Discussion section of this article.
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2.5) Sizes of priority groups given or referenced
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16
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No
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This is not detailed, even
though some data are fairly readily available (i.e. the size of the health care
workforce, the essential services workforce and numbers of people with chronic
conditions such as diabetes—as per the latest NZ Health
Survey11).
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2.6) Provision of storage for vaccines described
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12
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No
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The plan was written before
a supply of pre-pandemic vaccine was subsequently imported into NZ.
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2.7) Operational plan for the distribution of
vaccines
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14
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No
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The plan says this is still
being developed: “The Ministry of Health is working on the logistics of
mounting a mass immunisation campaign. This will be published as guidance for
DHBs who will be tasked with operationalising such a campaign, if
required” (p99).
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2.8) Specifies which healthcare workers will administer
vaccine
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11
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No
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The role of district health
boards (DHBs) is specified (p33), but not to the type of health worker level of
detail.
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2.9) Provisions of medical equipment (needles, syringes)
to support vaccine administration
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9
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Yes (p99)
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The plan states: “NZ
has in store sufficient needles/syringes, sharps containers and other
vaccination equipment and supplies to mount a mass vaccination
campaign.”
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2.10) Tender for H5N1 vaccine procurement
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5
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Partly (p99)
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The plan states: “The
purchase of a small quantity of vaccine effective against a clade of the H5N1
influenza virus is being considered. Such vaccines are still in
development” (p99). (Since this time a stockpile of such vaccine has been
purchased12).
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2.11) Secured pre-purchase agreement with vaccine
companies for the supply of pandemic strain vaccine
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4
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Yes (p99)
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The plan refers to a
pre-existing arrangement with an Australian manufacturer.
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Total (out of 11 categories)
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5.3/11.0
(average)
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4.5/
11.0
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(Or 3.0/11.0 for the NZ
plan using the alternative more stringent scoring approach).
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Measures detailed in the plan
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For 29 European
countries (N)
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For
NZ
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Comment with regard
to the NZ plan
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3.1) Strategic plan for the use of antivirals
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28
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Yes (p172)
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The plan refers to the use
of antivirals as part of border control, for cluster control and for reducing
morbidity and mortality from pandemic influenza (see Appendix I in the
plan).
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3.2) Specifies which antivirals will be used
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22
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Yes (p99)
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Oseltamivir
(Tamiflu) is the antiviral referred to. However, there is no mention of
amantadine or zanamivir (Relenza).
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3.3) Doses and duration of treatment recommended in the
plan
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20
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Yes (p173)
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See Appendix I in the
plan.
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3.4) Strategy for antiviral use in early
containment
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18
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Yes (p47)
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As part of intensive
cluster control operations antivirals will be offered to close contacts (unless
surveillance indicates clusters are already too widespread to attempt
control).
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3.5) Plans to use antivirals in people working with
animals/birds during animal outbreak
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20
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Partly (p28)
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This is probably implicit
in the statement: “Ensure appropriate protection and training for animal
workers and exposed humans (poultry and pigs most likely) to reflect WHO
guidelines and NZ guidelines and legislation.”
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3.6) Antivirals planned for treatment
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28
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Yes (p94)
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The plan states that:
“If and when the pandemic becomes more widespread within NZ, it is
anticipated that antivirals will be reserved for the treatment of cases.”
Elsewhere an antiviral distribution role is suggested for community-based
assessment centres (CBACs)—“to those meeting agreed clinical
criteria” (p97).
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3.7) Antivirals planned for pre-exposure prophylaxis
during a pandemic
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22
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Yes
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See item 3.1 above on use
in cluster control. In such settings antivirals can be used for people defined
as contacts and for those living in a defined area where cases have occurred
(and hence the antivirals will function as pre-exposure prophylaxis).
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3.8) Antiviral use for treatment explicitly prioritized
over that for prophylaxis
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15
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Yes (p170)
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The plan states that:
“in general, it is anticipated that National Reserve medication will be
used for the early treatment of people who become ill, rather than for
prophylaxis.” Also: “The NZ Pandemic Influenza Technical Advisory
Group concurs with the WHO opinion that pre-exposure prophylaxis for the
population at large, or for the workforce in general, is neither practical nor
possible because of the very large volume of medication required. The use of
National Reserve stocks in this way would unreasonably deprive many people of
any chance of treatment should they become ill.”
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3.9) Priority groups for treatment defined
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19
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Partly (p172)
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The plan argues that it is
not justified to be too specific at this point in time concerning prioritisation
policies and criteria (p172). But it also states that “Should
prioritisation become necessary, medication will be prioritised towards
population groups that are suffering poorer outcomes in terms of morbidity
and/or mortality AND who appear to be able to benefit most from antiviral
medication, and to people who provide certain identified services and functions
essential for effective direct pandemic responses.” (See the
Discussion below for further comment).
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3.10) Priority groups for prophylaxis defined
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22
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Yes
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See the response to item
3.1 above (regarding border control and cluster control). Furthermore, the plan
states that those on home quarantine may be on antiviral prophylaxis
(p41).
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3.11) Sizes of priority groups given or referenced
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16
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No
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See responses to item 2.5
above.
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3.12) Provisions for storage described
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15
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Yes (p168)
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The plan states that:
“supplies are stored in several locations in NZ, with ready-use supplies
available to support a rapid response anywhere in the country within a few
hours.”
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3.13) Operational distribution plan for antivirals
described
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18
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Partly
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It is implied that such
details exist but they are not spelled out in great detail: “Prepare for
the release of National Reserve volumes of antivirals, and consider
pre-positioning bulk supplies” (p39). Also: “Release antivirals for
use according to policy in border management operations” (p44).
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3.14) Named centres for local distribution
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13
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Partly
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See item 3.6 above
regarding CBACs.
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3.15) Requirement for prescription for antivirals
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11
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Yes (p173)
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There is no mention of any
plans to change this status in a pandemic setting.
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3.16) Country documents existing stockpile of
antivirals
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14
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Yes (p168)
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The precise size of the
national reserve is not stated in the plan but this has been made publicly
available by the Ministry (i.e. 855,000
courses13).
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3.17) There is antiviral stockpile reserved specifically
for early containment
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6
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Partly
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It is planned to use some
of the stockpile for cluster control (see item 3.4 above). However a set
proportion of the stockpile has not been designated for this specific use (which
might be appropriate given the advantages of a flexible response).
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Total (out of 17 categories)
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10.6/17.0
(average)
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13.5/17.0
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(Or 11.0/17.0 for the NZ
plan using the alternative more stringent scoring approach).
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In addition to the scoring process, the plan comparison
resulted in various gaps in the NZ plan being identified. These gaps are briefly
outlined in the tables with the major ones being around priority groups (Tables
3 and 4) and a strategic plan for pneumococcal vaccination (Table 3).
Discussion
Main findings and interpretation—The
use of this framework suggests that the version 16 (current) NZ pandemic plan is
generally more detailed relative to the average European plan (for those that
were also available in 2006). This finding is reassuring, especially considering
that the framework used had somewhat of a European focus. That is it included
countries that are generally both larger and wealthier per capita than NZ and
which sometimes even had their own influenza vaccine production facilities
(8/29) or actual plans to develop influenza vaccine production capacity (4/29).
Some also have their own capacity to produce antivirals and
all at least have near neighbours with vaccine/pharmaceutical industrial
capacity. Furthermore, the framework ignored various social distancing
interventions that might have allowed the NZ plan to score relatively more
highly (see the limitations subsection below). Another possible disadvantage for
NZ was that some of its planning work was in supporting documents that were not
considered in this analysis of plans (e.g. work on ethical
issues10 and evaluations of the simulation
exercises that have been conducted).
The relatively favourable scores for aspects of the NZ plan
are perhaps not surprising given the number of revisions the plan has undergone
(currently at version 16), and the fact that the plan has benefited from fairly
rigorous testing over several years.5 New
Zealand society may also be relatively good at such planning given its small
size, the relatively simple system of government (no state/federal system), and
the fact that it needs to plan for a relatively high occurrence of other natural
disasters (particularly floods, earthquakes, and volcanic events).
Nevertheless, the NZ plan is not very explicit on the issues
of priority groups for vaccination and antivirals (e.g. items 2.4 and 3.9). Even
so, the work from the National Ethics Advisory Committee
(NEAC)10 would appear to justify being more
explicit around frontline health workers being a priority group for both
vaccines and antivirals. The NEAC noted that: “Opinion polls in NZ have
suggested strong public support for the idea that frontline health workers
should receive priority access to antiviral medication. This suggests
reciprocity is a shared public value...”. (The opinion poll was reported
in 200613). Similarly, other NEAC statements
around patients who meet clinical criteria for care in normal times can be
interpreted as also favouring the use of vaccination and antivirals for those
who have greatest need.
These population groups include those already eligible for
fully-subsidised seasonal influenza vaccine on the grounds of increased risk of
adverse health outcomes from influenza infection. Being more explicit at a
planning stage on prioritisation issues may give additional reassurance to key
workers and reduce absenteeism in times of crisis (e.g. as was seen among some
healthcare workers during the SARS epidemic). While the flexibility to change
approach in light of the particular characteristics of a new pandemic strain is
desirable, the scientific community probably knows enough about pandemic and
seasonal influenza to still make reasonably detailed plans in the pre-pandemic
period.
Indeed, 21 out of 22 of the European plans that covered
pre-exposure antiviral prophylaxis suggested that health care workers be
recipients of these.9 Another study of 31
countries reported that 84% had identified at least one priority group (and that
health care workers were identified in all of
these).14 As well as most other countries with
plans having identified priority groups for scarce resources such as vaccines
and antivirals,15 a number of these groups are
specifically listed in WHO guidelines (tabulated
elsewhere15). The most sophisticated
prioritisation work to date may also help guide prioritisation efforts around
different age groups based on years of life
lost16 (albeit with potential adjustment as
information on the new pandemic strain emerges). A recent major US report also
highlights the need for an ethical framework to allow for prioritisation of
antivirals.17
In line with these arguments, the Ministry of Health appears
to be considering some prioritisation for its use of pre-pandemic
vaccine. As stated on its website: “key front-line health workers and
other front-line pandemic response personnel” are prioritised for this
vaccine in its draft considerations.12
Prioritisation of antivirals is however far more complex given the trade-offs
between potential use for the treatment of sick individuals at high risk of
death and pre-exposure prophylaxis of front-line healthcare workers. The WHO
recommends saving antiviral supplies for the former while Norway has explicitly
prioritised antiviral prophylaxis for continuously exposed health care workers
over treatment of sick patients so as to maintain a functioning health
service.9
A further possible weakness of the NZ plan is the lack of
specific attention to pandemic planning around avoiding the further exacerbation
of health inequalities for already disadvantaged populations (as raised in the
international literature18). The 1918 influenza
pandemic had a disproportionately severe impact on Māori
mortality19,20 and recent NZ research also
indicates higher seasonal influenza hospitalisation rates among those in crowded
housing and with young children.21
Another area in the NZ plan that could be strengthened is
including discussion of pneumococcal vaccination (item 2.2). There is some new
evidence for the impact of pneumococcal vaccine on reducing invasive disease in
those aged 65 years and over.22 An earlier
Cochrane systematic review also identified a benefit for preventing invasive
pneumococcal disease (but not the incidence of pneumonia or death in adults with
or without chronic illness).23 Various authors
have recently argued for considering this vaccine in pandemic
planning.24
Although NZ has taken an alternative path of stockpiling
antibiotics, it could be that use of pre-pandemic pneumococcal vaccination is
also worth considering and might provide additional reassurance (since it is
less dependent on continued health service functioning). At least there could be
evidence in the NZ plan that these issues have been given appropriate
consideration by relevant experts.
Limitations of this analysis—This
brief analysis has a number of limitations. A major one is that the framework
used only focused on the domains of border control, vaccines, and antivirals. In
particular the importance of quarantine appears to be under-rated in this
framework and plans for various other non-pharmaceutical interventions are not
considered at all: education strategies to reduce incoming traveller numbers;
community restrictions such as school and workplace closures; media campaigns to
promote hand hygiene and cough etiquette; strengthening surveillance systems;
improving access to rapid diagnostic tests; promoting systems that allow remote
diagnosis (e.g. via video-links over the Internet); contract tracing systems;
and the promotion of voluntary sheltering (i.e. voluntary sequestration of
healthy people to avoid exposure).
Furthermore, plans can also potentially have
country-specific research agendas for pandemic preparedness and can demonstrate
a “whole-of-government” approach to planning and these items are not
in the framework used. If these issues had been considered in the framework,
then the NZ plan may well have scored even higher relative to the average
European plan since it does give consideration to many of these issues.
Another limitation of the framework used was that it does
not weight variables according the country-specific characteristics (e.g.
available resources such as vaccine production capacity mentioned above, and
geographical isolation). For example, item 1.3 (mentioning following WHO
recommendations on travel) was an item where the NZ plan scored
“zero”. Yet this criterion might not be that appropriate for an
island nation such as NZ which may wish to take a particularly rigorous approach
to border control. Furthermore, WHO guidelines are fairly general and there is
relatively little consideration of the special issues facing remote island
nations in any WHO documents on pandemic influenza published to date.
Possibly the ideal is for there to be WHO pandemic plan
assessment frameworks and guidelines that are more tailored to different types
of countries and especially for island nations (given that islands may have more
scope for border control and within-country control). Such frameworks could come
with detailed scoring systems to allow more sophisticated approaches to
quantifiable plan comparisons. This refinement would prevent the fairly crude
approach to scoring undertaken in this article (i.e. where we could no obtain
the data extraction tool used in the European analysis).
Earlier work by Mounier-Jack and
Coker25 has been somewhat criticised for not
including any site visits.26 These critics
state that “the experience of the national assessments during country
visits has demonstrated that looking at plans alone often gives an incomplete
and sometimes misleading picture of a country’s state of
preparedness.” These critics also noted that the pandemic plans in many of
these European countries were rapidly superseded as a result of ongoing planning
developments. These issues may also apply to some extent to this 2007
publication of European plans by Mounier-Jack et al that was used in this
analysis. Nevertheless, this problem is largely unavoidable without conducting
very much more expensive studies (with site visits) that are published quickly
outside of the journal literature (i.e. without lengthy peer review and
publishing processes).
Finally, the data extraction from the NZ plan for comparison
purposes was done by only one person (NW) with no assessment for inter-observer
reliability. Nevertheless, both authors do have a high level of familiarity with
the content of this NZ plan as a result of ongoing research work around
influenza control in recent years for different agencies.
Possible implications
for future NZ planning—Based on the results and discussion above,
the following specific issues could be addressed in the next (probably to appear
in 2009) version of New Zealand’s pandemic plan. Some of these points may
also be relevant for DHB level plans:
- Consider
the addition of more explicit details on the priority groups for vaccination,
antivirals (for both treatment and prophylaxis) and other potentially limited
resources (e.g. personal protective equipment). These details could extend to
the different types of health workers (e.g. hospital doctors and nurses, primary
care health workers, ambulance staff) and the different types of essential
workers (e.g. police, fire-fighters, border control workers, defence personnel).
In addition it may be desirable to specifically mention those who are currently
eligible for fully-subsidised influenza vaccine due to increased risk of adverse
sequelae (e.g. those over 65 years, and those with chronic heart disease,
chronic respiratory disease, asthma treated with inhaled steroids).
Additional pandemic
control provisions for the most needy New Zealanders could also be considered
(e.g. those living in deprived areas, in crowded houses, and with large numbers
of children in the house).
- Consider
adding discussion of pneumococcal vaccination in the NZ plan (item 2.2 and
discussed above).
- Consider
various additions that are covered in the framework for border control (item
1.9) and with regard to vaccines (items 2.3,
2.5–2.8).
Furthermore, the NZ health sector
could consider further studies of the pandemic plans of other countries (to see
if additional lessons can be learnt), and could further expand its own pandemic
research agenda.27,28 Possible priority plans
are those from countries which have recently tested their plans in simulation
exercises (e.g. Singapore, UK,29
France,30 and
Australia31,32).
Other reviews of pandemic plans from multiple
countries7,15 and of sub-national plans (e.g.
of US states33) may also be worthy of further
examination.
Competing interests: Both authors have
undertaken past contract work on pandemic influenza epidemiology for the
Ministry of Health, but have not participated in the drafting of the pandemic
plan examined in this article. They have no other competing interests.
Author information: Nick Wilson, Senior
Lecturer, Department of Public Health, University of Otago, Wellington; Michael
G Baker, Associate Professor, Department of Public Health, University of Otago,
Wellington
Acknowledgements: We thank the Ministry of
Health for providing funding support for earlier aspects of this work (prepared
in a section of a literature review for the Ministry) and for providing comment
on an earlier draft of the manuscript. We note, however, that the views
expressed do not necessarily reflect current Ministry of Health policy. We also
thank the anonymous reviewers for the Journal who provided helpful
critical comment on the manuscript.
Correspondence: Dr Nick Wilson, Department
of Public Health, University of Otago Wellington, PO Box 7343 Wellington South,
New Zealand. Email nick.wilson@otago.ac.nz
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