|
A regional LabNet
workshop from 8 to 10 September 2003 followed the first EpiNet workshop
in the previous week. The first two days were held at the Holiday Inn
Hotel in Suva and the third day at Mataika House. It was
co-organised by the Secretariat of the Pacific Community (SPC) and the
World Health Organization (WHO) in collaboration with
the New Caledonia
Pasteur Institute (IPNC).
The objectives of the
meeting were to:
 |
update the
participants on the progress of LabNet development;
|
 |
assess the current
situation of laboratory testing and specimen shipment with regards
to Pacific Public Health Surveillance Network (PPHSN) target
diseases, including SARS, and plan further developments; |
 |
review and discuss
the linkages and support available through reference laboratories of
the Australian and New Zealand Public Health Laboratory Network;
|
 |
discuss and
clarify laboratory techniques available for the PPHSN target
diseases; |
 |
become familiar
with the use of rapid tests (leptospirosis, dengue and influenza)
and DVBS (measles); |
 |
assess training
needs of laboratory health professionals;
|
 |
update the
participants about lab-specific bioterrorism issues and discuss
practical lab-related aspects;
|
 |
discuss and agree
on possible lab-based surveillance activities.
|
Participants were
laboratory professionals* members of
national/territorial EpiNet teams from all the Pacific
Island countries and territories, except the Commonwealth of the Northern
Mariana Islands, Papua New Guinea, and Wallis and Futuna (who could not
attend). Most of the members also participated in the EpiNet workshop.
Additional experts were invited to assist in specific technical areas and/or
as PPHSN allied members.
The format of the first
two days was the same as for the EpiNet workshop: plenary presentations and
discussions, group work and panel discussions. The third day included
hands-on exercises with rapid tests. An overview of the workshop proceedings
is presented below.
Day 1:
Strengthening the network and bioterrorism
Chairperson: Mrs Vasiti Uluiviti, American Samoa
Rapporteur: Mr Taukea Okesene, Niue
After a short opening
ceremony, the representative of the New Caledonia Pasteur Institute (IPNC), the
institution with leadership in the LabNet Technical Working Body (TWB), gave a
presentation on the origins and development of LabNet.
The sessions included:
 |
Assessment of
current capacity of the network
plenary presentations of L2
laboratories (New Caledonia Pasteur Institute, Mataika House
in Fiji,
Guam Public Health Laboratory and French Polynesia Malardι
Institute); |
 |
Lab-specific
bioterrorism issues plenary presentations on the global anthrax
laboratory network and laboratory preparedness for bioterrorism and
outbreak-prone diseases in the Northern Pacific; |
 |
Lab-specific
training needs one plenary presentation of the Pacific Paramedical
Training Centre (PPTC) including the Regional External Quality
Assurance Programme. |
A series of issues came
out of the discussions held after the presentations:
 |
the shipment of
specimens to other laboratories for confirmation testing
|
 |
the number of
specimens needed to be tested to confirm an outbreak
|
 |
the linkages
between L1 and L2 laboratories to be strengthened
|
 |
the development of
a website for laboratory personnel
|
 |
the production of
guidelines for quick response
|
 |
the training of
laboratory personnel |
 |
personal safety
procedures, with proper handling of specimens and use of safety
equipments to be emphasised
|
After that, three working
groups discussed training needs and Quality Assurance (QA) programmes.
Laboratory training
needs
Each group identified different training needs. They included in-country
training, overseas training, training to keep equipment to standard, IATA
packaging and regulations, distance training, a link to
a Palau proposal for
training at Palau Community College (PCC), credit and recognition for each
course from an academic institution (PCC, Fiji School of Medicine, etc.),
coordination by Pacific Paramedical Training Centre (PPTC), gradually
building to certificate and diploma.
Quality Assurance
(QA) and Quality Control (QC)
All groups agreed that the External Quality Assurance programme run by PPTC
should continue. They also recommended that an internal QA programme be
encouraged and performed on a regular basis.
During the discussions it was
also recommended that:
 |
PPHSN target
diseases should be incorporated into QA programme (for those not yet
included); |
 |
regular meetings
on aspects of QA should be organised with clinicians;
|
 |
information should
be exchanged and shared more readily;
|
 |
laboratory
auditing should be organised among PICTs;
|
 |
an inventory of
QA/QC programmes, policies, and protocols of all PICTs laboratories
should be completed; |
 |
PPHSN should
request PPTC to provide QA/QC for all PICTs laboratories and provide
standardisation; § |
 |
teaching
institutions should have standard teaching materials; and
|
 |
PPHSN should
request the National Reference Laboratory in Melbourne, Australia, to
support PICTs laboratories in very specific areas (e.g. serology).
|
As a result, a technical
group was formed the next day to prepare a QA plan of operations. The core
members are IPNC, PPTC, SPC and WHO, with PPTC as focal point. Supporting
members include L2 and L3 laboratories and training institutions (Fiji
School of Medicine, Palau Area Health Education Center). The role of the
technical group is to strengthen QA through PPTC.
The members agreed on the
following priorities:
 |
PPHSN allied
membership and a review
of status of memorandum of understanding
(particularly with PPTC-WHO)
should be organised under the PPHSN framework by the end of 2003.
|
 |
QC should be
extended to the shipment of dengue and leptospirosis, measles and
influenza samples, depending on PICT priorities (typhoid and cholera are
already included). |
 |
Auditing conducted
by PPTC should be continued and the recommendations should be passed
on to the PPHSN QA technical group for further action (regional and
political). Internal QC promotion and supervision should also be
included in the process.
|
 |
The output of
the WPRO
laboratory meeting at the end of October 2003 should be taken into
account. |
 |
Standard operating
procedures (SOPs) should be shared. Examples of laboratory handbooks
for clinicians from Tonga, Fiji Islands and Samoa should be posted
on the PPHSN website and PacNet by the end of 2003.
|
 |
PPHSN guidelines
should include SOPs, and should be used as references, as soon as
finalised (beginning 2004).
|
 |
PPTC should design
training according to QC results as of 2004. This should be
implemented as from 2005, with support from PPHSN other allied
bodies/partners (Fiji School of Medicine, Palau Area Health
Education Center) and using PPHSN guidelines as reference. PPTC
should continue with the management and QA training programme. PICTs (e.g.
ministries of
health) should be used as alternative training sites.
|
Day 2:
Technical update Strengthening the network
Chairperson: Mr Andrew Darcy, Solomon Islands
Rapporteur: Mr Raymond Seule, Vanuatu
The focus of the second
day was on laboratory techniques for PPHSN target diseases and regional
support.
The first session included
plenary presentations on laboratory techniques for influenza, leptospirosis,
typhoid and dengue, as well as Dried Venous Blood Spot (DVBS) specimens for
measles.
Subsequent sessions covered the following
three themes:
 |
Lab-based surveillance activities
|
 |
Regional support (including
presentations on the Australian Public Health Laboratory Network,
public health laboratory services in New Zealand (Environmental
Science and Research Ltd), the
Victorian Infectious Diseases Reference Laboratory, the influenza
laboratory network and practical aspects of specimen shipment)
|
 |
LabNet development planning |
Two groups examined the question: How can L2
and L3 laboratories assist the L1 laboratories?
 |
Training
organise
training/certification on IATA packaging/shipping, training
of trainers in the same area, and technical training of staff.
|
 |
Technical support
develop
guidelines for diagnosis confirmation (including specimen needed and
test available). |
 |
Supplies/stockpiles
arrange one
stockpile per country/hospital. Delays in shipment
of supplies should be
minimized, with key person being responsible for shipping.
|
 |
Testing guidelines
L2
laboratories could provide support for the six PPHSN target diseases
plus others (STIs, HIV, TB). The latest laboratory manuals and
protocols for target diseases should be available. |
 |
Communication
PPHSN should
try to make sure that each laboratory has Internet access, to
facilitate the sharing of information and
communication of laboratory results. An electronic list server of L2 and L3 contact
persons should be available.
|
 |
Overseas testing
laboratories should acknowledge
receipt of the specimens and try to quickly return the results. This
would avoid anxiety for the sender and accelerate the notification
to the physician and the initiation of patient management.
|
 |
Other issues
L2
laboratories should be able to provide test kits (e.g. rapid test
for lepto, etc.) in case they are needed by an L1 laboratory.
Current capacities of the laboratories should be
assessed.
An MOU between L1, L2 and L3 laboratories should be
prepared. |
Day 3
The last day included
hands-on exercises with rapid tests. Participants were familiarised with
rapid tests for leptospirosis, influenza, dengue and the
DVBS technique for
measles specimens.
Copies of the latest draft
of the PPHSN Strategic Plan, including EpiNet and LabNet aspects, were
distributed to all the participants.

*
Palau was represented by a public health physician.
[
Back
to IA16 Table of Contents ] [
Back to PPHSN Website ]
|