CCSG minutes Ottawa October 2004
Minutes of meeting of the
Cochrane Collaboration Steering Group
[These minutes were approved by the Steering Group
Executive on 22 November 2004]
Subject
|
Item
|
Advisory
Group budgets |
|
Advisory
Group, Cochrane CENTRAL |
|
[Advisory] Group, Cochrane
Library Users’ |
|
Advisory Group, Colloquium
Policy |
|
Advisory Group, Criticism
Management |
|
Advisory Group, Handbook |
|
[Advisory] Group,
Information Management System |
|
Advisory Group, Quality |
|
Advisory groups, future
Steering Group membership of |
|
Advisory groups,
reimbursement of convenors and members |
|
Annual General Meetings,
agenda and format of the |
|
BMJ/Clinical Evidence,
relationship with |
|
Book series, agreement on |
|
Campbell Collaboration,
liaison |
|
Centres, commercial
sponsorship of |
|
Centres, report from entity
representatives |
|
Centres, revision of
section in The Cochrane Manual |
|
Chief Executive Officer,
position of the |
|
Chief Executive Officer,
report from the |
|
Chris Silagy Prize,
commitment to the |
|
Clinical trials,
prospective registration of |
|
Cochrane [Exchange]
Fellowship, revised name and timetable for |
|
Cochrane Library,
complimentary copies of The |
|
Cochrane Manual, revision
of section on Centres |
|
Cochrane Reviews, creation
of umbrella (summary) reviews |
|
Cochrane Reviews of
diagnostic test accuracy |
|
Cochrane Reviews,
plagiarism within |
|
Cochrane Reviews,
prioritisation of key topic |
|
Collaborative Review
Groups, guiding principles for |
|
Collaborative Review
Groups, report from entity representatives |
|
Colloquia, filming of
sessions |
|
Colloquium Manager,
proposal for development of |
|
Colloquium, Dublin, 2006 |
|
Colloquium, Melbourne, 2005 |
|
Colloquium, São Paulo, 2007 |
|
Commercial sponsorship,
Cochrane Collaboration policy on |
|
Commercial sponsorship,
ambiguities in the policy |
|
Commercial sponsorship,
position of Centres |
|
Company Secretary, job
description of |
|
CONSORT Statement,
endorsement of the |
|
Consumer Network |
|
Contact Database, suggested
amendment to terms of use of |
|
Contingency Fund
expenditure |
|
Contingency plan |
|
Declarations of interest by
everyone involved in the review process |
|
Declarations of interest by
Steering Group members, |
|
Derivative products,
commercial sponsorship of |
|
Developing countries
initiative |
|
Diagnostic Test Accuracy
Working Group |
|
Discretionary Fund
expenditure |
|
Donations, central fund or
foundation for receiving unrestricted |
|
Editors, gender balance of |
|
Elections, information on
candidates |
|
Entity representatives,
verbal reports from |
|
[Exchange] Fellowship,
revised name and timetable for |
|
Fields/Networks, report
from entity representatives |
|
Finance, advisory group
budgets |
|
Finance, allocation of
expenditure between financial years |
|
Finance, cash flow forecast
and current financial position |
|
Finance,
Contingency and Discretionary Fund expenditure |
|
Finance, recommendations
about the size and purpose of the Contingency Fund |
|
Finance, reimbursement of
sub- and advisory group convenors and members |
|
Funders’ Forum, report from |
|
Funding Arbiter, report
from |
|
Funding working group |
|
Funding, European Union |
|
Funding, foundation |
|
Funding, monthly newsletter
from Chief Executive Officer |
|
Global review of access to
healthcare information |
|
Guidelines International
Network, relationship with |
|
Information Management
System, status of |
|
Information Management
System, name for new server |
|
James Lind Alliance,
relationship with the |
|
Job description, Co-Chair
of the Steering Group |
|
Job description, Company
Secretary |
|
Job description, Funding
Arbiter |
|
Job description, Ombudsmen |
|
Job description,
Publication Arbiter |
|
Job description, Steering
Group members |
|
Kenneth Warren Prize 2004 |
|
Mazars LLP, acceptance of |
|
MeerKat, support and
development of |
|
Methodological quality
improvement projects |
|
Methods Groups, report from
entity representative |
|
Mid-year meeting of
Steering Group in Thailand in 2006 |
|
Monitoring and Registration
Group, report from the |
|
Monitoring, frequency of |
|
Non-randomised studies and
specialised registers |
|
Ombudsmen, report from the |
|
Priority setting for the
next four years |
|
Prospective registration of
clinical trials |
|
Publication Arbiter |
|
Quality improvement
projects, methodological |
|
Risk assessment, table of |
|
Specialised registers,
non-randomised studies and |
|
Steering Group elections,
information on candidates |
|
Steering Group members,
verbal reports from outgoing |
|
Steering Group membership
of sub- and advisory groups, proposed |
|
Steering Group mid-year
meetings |
|
Steering Group, monitoring
the |
|
Steering Group, next five
meetings of the |
|
Steering Group, procedure
for selecting a Chair of |
|
Strategic Plan in relation
to the Information Management System |
|
Treasurer, report and
financial statements |
|
Trading Company Directors,
issues raised by the |
|
Visiting Fellowship
(formerly called ‘Exchange’ Fellowship) |
|
Website development project |
|
Wiley, report from |
Minutes of the meeting of the
Cochrane Collaboration Steering Group
Ottawa, Canada
1 and 4 October 2004
[These minutes were approved by the Steering Group
Executive on 22 November 2004.]
Present (Steering Group members shown in bold typeface): Godwin Aja, Claire Allen, Gerd
Antes (on 1 October only), Lorne Becker (on 4 October only), Lisa
Bero, Kathie Clark, Mike Clarke (on 1 October only; Chair on
1 October, but absent for item 11 on methodological quality improvement
projects), Mark Davies, Jon Deeks, Kay Dickersin (only for item
22.12 on the Publication Arbiter’s report on 4 October), Deborah Dixon (for
item 10 only), Zbys Fedorowicz, Dan Fox (only for item 22.14 on the
Funders’ Forum on 1 October), Davina Ghersi, Sally Green,
David Henderson-Smart (on 1 October, and only for item 22.12 on the
Publication Arbiter’s report on 4 October), Jini Hetherington (minutes), Louise
Kitchener (until noon on 1 October), Monica Kjeldstrøm, Carol Lefebvre (only
for item 10, the report from Wiley representatives regarding search testing the
Wiley InterScience site, on 1 October), Steff Lewis, Jim Neilson
(Chair on 4 October), Jordi Pardo, Deborah Pentesco-Gilbert (for item 10
only), Nick Royle (absent from discussion about renewal of the CEO’s contract –
item 6), Rob Scholten, Silvana Simi (on 1 October only), Haluk
Soydan (on 4 October only), Peter Tugwell, Janet Wale and Liz
Waters.
1.
Welcomes,
apologies for absence, introductions, and approval of the agenda
Mike welcomed everyone to the
meeting, and introduced the incoming members of the Steering Group, Godwin Aja
(representing the Consumer Network), Lisa Bero (representing Centres), Zbys
Fedorowicz (representing CRGs), Rob Scholten (representing Centres) and Liz
Waters (representing Fields). Mike
explained that Lorne Becker, sharing the position of Field Representative with
Liz Waters, would join the second Steering Group meeting on 4 October. For the benefit of the incoming members,
Mike explained that Steering Group meetings during Colloquia are a day shorter
than the mid-year meetings, due to time constraints. The agenda was approved.
2.
Declarations of
interest of Steering Group members, IMS Director, and Secretariat staff
2.1 Current declarations: Mike invited people to mention any changes
to their current declarations of interest, which had been included with the
agenda for this meeting, and would form an appendix to these minutes; there
were no changes. It was agreed that
guidance as to what should be disclosed in such declarations would be helpful,
as would a standard format. Lisa
volunteered to provide a template for discussion at the next Steering Group
meeting in Providence in April 2005.
Action: Lisa
2.2 Should everyone involved in the
review process (including editors and referees) make declarations of interest
in Cochrane reviews? It was pointed out that potential conflicts of
interest of editors should be declared in the CRG modules published in The
Cochrane Library, and the CRG representatives were asked to remind their
constituents of this. It was suggested
that referees should also be encouraged to declare their potential conflicts of
interest to their CRG(s). It was not
thought to be necessary to declare these conflicts within individual reviews.
Action: CRG representatives
3. Matters arising from the minutes of the
previous meeting
Mike reminded everyone that the
minutes of the mid-year Steering Group meeting in Bergamo had been approved by
the Executive in a teleconference in March 2004. The following matters arising
from those minutes were discussed:
Item 5.2 - Allocation of expenditure between financial years: Nick reminded everyone that the default
policy is that the Collaboration does not pay institutional overheads on grants
to other legal entities. In cases where
a contribution to indirect overheads is requested and refusal to pay these
costs would impact negatively on the Collaboration's ability to function
effectively, each case should be referred to the Steering Group for
consideration by its Executive, which would make a recommendation. A statement to this effect is contained in
The Cochrane Manual.
Item 18 – Proposal for MeerKat support and development: Nick reported that the MeerKat Working Group
has continued to work on a revised budget since the Steering Group meeting in
Bergamo, after discussions with the Information Management System Group. The revised budget has not yet been formally
presented to the Steering Group, and Nick agreed to follow this up so that it
can be brought to a future Executive teleconference for approval.
Action: Nick
Item 21.1 – Plagiarism within Cochrane reviews: Mike explained that preparation of a policy
document on plagiarism was still in progress.
Sally asked that the editors of the Cochrane Reviewers’ Handbook (Phil
Alderson, Julian Higgins and herself) be sent an early draft of this to comment
on, since the policy will eventually be included in the Handbook.
Action: Mike
Item 21.4.2.2 - Guiding principles for CRGs: Peter and Davina said they were still in the process of preparing
a similar document to ‘Guiding principles for Centre Directors and Centre
staff’ for CRGs, and would report to the Steering Group at its next meeting in
Providence in April 2005.
Action: Peter, Davina
4.
Report from the
Co-Chairs
Neither Jim nor Mike had anything to
report that had not been included on the agenda of this meeting.
5.
Report from the
Chief Executive Officer
5.1 Book series: Nick reported that
negotiations for a book series had been concluded, and an agreement had
recently been signed between The Cochrane Collaboration and Wiley. (See also item 18 below.)
5.2 Prospective registration of clinical
trials: Nick said that he would be meeting in New York with people
interested in this initiative at the end of October 2004, and would report back
to the Steering Group by e-mail.
Action: Nick
5.3 Global review of access to healthcare
information: Nick reported that the Collaboration is a
core participant in this project looking at access to healthcare information in
developing countries, and will be preparing the section on access to systematic
reviews. The project is being conducted
under the auspices of INASP and WHO, and Paul Chinnock of the Injuries Group is
taking the lead on behalf of the Collaboration. It is expected that there will be a final report to the Steering
Group during the Melbourne Colloquium in October 2005, although doubts have
arisen recently about the stability of INASP’s funding for the project.
5.4 Funding newsletter: Nick invited
feedback on the usefulness of his monthly funding newsletter.
5.5 Funding working group: This group
(comprising Gerd, Jim, Jon, Kathie [who replaced Mike], Mark, Nick and Nandi)
has met once by teleconference and is in the process of establishing its remit
and an action plan.
5.6 Commercial sponsorship: Nick is in
discussions with the Association of the British Pharmaceutical Industry (ABPI)
about funding initiatives within the context of the Collaboration's policy on
commercial sponsorship.
5.7 European Union funding: The
Collaboration’s work does not fit into the EU’s current call for applications
for funding, but Nick reported that he was hopeful that a future call would be
more relevant.
5.8 Foundation funding: Nick hopes
to work on this area in the next few months.
5.9 Consumer Network issues: Nick
reported that the lengthy dispute had recently been resolved, and that the
Cochrane Collaboration Consumer Network Incorporated (CCCNI) is in the process
of being dissolved. Signed agreements
by the parties in the dispute are now in place. He thanked Janet in particular for her part in reaching a
resolution, and Sally and Janet both thanked him for all he had done to this
end. Sally reported that all the
documents of the CCCNI are archived at the Australasian Cochrane Centre. Kathie drew attention to the fact that any
change of legal status or governance (e.g. registering as a company or charity)
requires approval of the Monitoring and Registration Group. It was agreed that entities will be
discouraged in future from setting themselves up as separate legal entities.
6.
Report on
progress against objectives set at the Steering Group meeting in Melbourne in
March 2003, and priority setting for period 2005-06 to 2007-08
6.1 Progress
and priority setting for the next four years:
Nick was asked to develop this
draft document further for discussion at the next Steering Group meeting in
Providence. It was agreed that the
priority of developing consumer synopses for those reviews without a synopsis
should be reworded to include improving the quality of existing synopses. Janet agreed to bring recommendations from
the group working on synopses to the next Steering Group meeting in
Providence. Jon was asked to discuss
with methodologists their role in taking the lead in liaising with CRGs. Liz requested that Fields be more involved
in discussions about priorities in future.
It was agreed that the Collaboration’s Strategic Plan should be
discussed in detail at the next Steering Group meeting in Providence.
Action: Nick, Janet, Jon
6.2 Position of the Chief
Executive Officer: Nick’s two-year
contract as Chief Executive Officer (CEO) ends on 31 March 2005. He left the meeting for the discussion about
whether or not to maintain this post.
It was agreed that the Collaboration needs to continue employing a
CEO. Nick’s annual performance
appraisal should be conducted in the next month by a panel comprised of Jim and
Kathie (the Co-Chairs) and Jordi (who has the perspective of members of The
Cochrane Collaboration based in countries whose first language is not English). This panel will make a recommendation to the
Steering Group about renewal of Nick’s contract, and also about the optimum
length of the contract. The Co-Chairs
will ask Steering Group members for questions that should be asked as part of
Nick’s appraisal, and share these with Nick in advance.
Action: Jim, Kathie, Jordi
7. Report from the Treasurer - financial and legal
matters:
7.1 Report and Financial Statements: Jini
was asked to e-mail this year’s table of risk assessment to the Steering Group
for information.
Action: Jini
7.2 Acceptance of Mazars LLP (formerly
called Mazars): It was agreed that, if approved at the AGM,
the Collaboration would continue to accept Mazars LLP as its auditors, and Jini
would communicate this to the company.
Action: Jini
7.3 Issues raised by the Trading Company
Directors: Monica reported that according to the table of key
dates the Trading Company Directors and the Company Secretary had fulfilled all
their responsibilities so far this year.
The Directors had requested that information on the income from sales of
reprints and subscriptions to pharmaceutical companies should be declared by
Wiley in their quarterly breakdowns of royalty figures, and recommended that
the Steering Group should also review these figures on a regular basis. Jos Kleijnen is resigning from the board of
directors of the Trading Company at this year’s Annual General Meeting, and is
being replaced as Chair by Mike Clarke when Mike steps down from the Steering
Group on 3 October 2004. Monica
explained to new Steering Group members that the Collaboration holds 100% of
the shares of the Trading Company, and that the Trading Company passes all
surplus income to The Cochrane Collaboration.
Action: Nick
7.4 Cash flow forecast, and current financial
position: Nick presented the cash flow forecast and there was
discussion about the continuation of some of the current initiatives. This will be formally reviewed at the next
Steering Group meeting in Providence in 2005. The Chris Silagy Prize should be added to the cash flow
forecast as an ongoing commitment. Nick
clarified that the projected income figures on the cash flow forecast are based
on a ‘worst case’ scenario.
Action: Nick
7.5 Advisory Group budgets: Mike
drew attention to the document with the agenda materials which listed the
advisory group budgets that had been approved at the Steering Group meeting in
Bergamo in February/March 2004.
7.6 Contingency and Discretionary Fund
expenditure: Attention was drawn to the fact that only one
application had been made for Discretionary Fund support during the current
financial year. Entity representatives
should bring this opportunity to apply for resources to the attention of their
constituents.
Action: All entity representatives
7.7 Recommendations
regarding the size and purpose of the core Contingency Fund and related
contingency plan: It was agreed that one of the actions in the
contingency plan drafted by Nick should be the initiation of legal proceedings
if the loss of royalties is due to breach of contract, and an estimate of these
costs should be added to the proposed Contingency Fund of £150,000. Monica was asked to work out how much it
would cost to support the IMS team for twelve months, and to send that figure
to Nick, so that the Steering Group can come to a decision at a later date if
necessary about whether or not to include that figure in the Contingency
Fund. It was agreed that new IMS
developments would be put on hold should the Collaboration’s core income
collapse, and the contingency plan need to be activated. Nick was asked to e-mail a revised
contingency plan to the Steering Group, taking account of the agreed changes.
Action: Monica, Nick
7.8 Reimbursement to sub- and advisory
group convenors and members: Mike and Sally declared their conflict of interest as
advisory group convenors. There was
agreement that reimbursing advisory group convenors for their work as convenors
was not appropriate. It was agreed that
if there is a specific substantive project that needs to be done by an advisory
group to the Steering Group, the Executive should be asked for approval of
funding on a case-by-case basis.
7.9 Kenneth Warren Prize 2004: Mike
explained that this will be a standing item on Steering Group agendas in
future, to inform them of the current state of this restricted fund, which
currently amounts to approximately £22,700.
8. Information Management System
8.1 Status of the new IMS: Monica
reported that good progress was being made on the development of the new IMS,
as outlined in her report. The Cochrane
Collaboration has funded a system developer to work full-time on the new IMS on
a temporary contract. To ensure
continuity and maintain the developer expertise that exists within the IMS
team, Monica requested funding to retain this person on staff on a long-term
basis. This was agreed to in principle,
and Monica was asked to provide details and a budget for discussion by the Steering
Group at its next meeting in Providence, within the context of the current IMS
budget. Monica’s report should describe
this person’s particular skills and how ongoing IMS work contributes to the
Collaboration’s Strategic Plan. She
confirmed that the four CRGs pilot-testing the IMS are globally distributed.
Action: Monica
8.2 Name for new IMS server: There had been numerous suggestions as
to what the new IMS server should be named.
Monica confirmed that once the IMSG had agreed on their recommendation,
the Steering Group would be asked to cast the final vote.
Action: Monica
9. Cochrane Collaboration policy on
commercial sponsorship:
9.1 Ambiguities in the
sponsorship policy: Mark drew
attention to the fact that the Collaboration’s sponsorship policy is unclear as
to whether entities should be allowed to receive royalties from sales of
derivative products. It was agreed
that, due to the large potential variation in derivative products, the Steering
Group needs to assess the financing of derivative products on a case-by-case
basis when assessing the individual business plans for derivative
products. Such business plans should be
prepared by the proposers for each product and agreed by the publisher and the
Steering Group. It was noted that all
derivative products from The Cochrane Library need Steering Group
approval.
9.2 Position of Centres: The Centre Directors met in parallel with the Steering Group meeting on 1 October, and Gerd, Kathie and Sally were therefore absent from the Centre Directors’ meeting. Jordi said that the Centre Directors had asked to see the summary of feedback on the survey of all entities about commercial sponsorship of Centres, and this was agreed to. Feedback from Centre staff broadly supported the option of commercial funding for activities such as translations. Feedback from Co-ordinating Editors provided no clear consensus.
9.2.1 Discussion on 1 October 2004: Two options had been proposed in a paper
included with this agenda, based on the responses to the survey of all
entities:
(1) To prohibit direct commercial funding to Centres, as with Review Groups,
Fields, and the Consumer Network. This
option would have the attraction of clarity and simplicity, but could damage
existing activity by Centres and was not consistent with the varying tasks of
Centres, many of which are similar to Methods Groups; or
(2) To permit some direct commercial funding to Centres, but only of non-review
activity and with safeguards to maintain the ‘firewall’. If the Steering Group were to adopt this
option, there would be a need to specify which activities could and which could
not be supported by commercial sources.
After lengthy discussion, in which Steering Group members’ views were divided
almost equally, there was majority agreement to adopting the second
option. It was agreed that Centres
should be encouraged to divest themselves of current funding from commercial
sources, and to seek future funding which is not reliant on commercial
sources. Any future proposal to accept
funding from commercial sources should be brought to the Steering Group for
approval, and all sources of funding should be explicitly stated in Centres’
modules. The policy should be revisited
formally, as planned, in 2007.
Paragraph 8 of the sponsorship policy should be amended in the light of the
decision to adopt the second option.
This paragraph currently reads as follows:
”The situation with regard to Cochrane Centres is more complex than for other
Cochrane entities. For example, Centres can be both close to review production
(like Fields and the Consumer Network) but can also engage in methodological
work (like Methods Groups). It was agreed, therefore, that a further, short,
period of consultation should take place specifically in relation to the
sponsorship of Cochrane Centres by commercial sources.”
9.2.2 Discussion on 3 October
2004: This issue was
discussed in the open session of the Annual General Meetings of The Cochrane
Collaboration and the Collaboration Trading Company on 3 October 2004. Jim described the previous consultation on
commercial sponsorship, and the more recent survey of all entities that had
been conducted by the four Centre representatives on the Steering Group. These had shown no clear consensus about the
position of Centres. On the basis of
these results, and after lengthy discussion, the Steering Group had decided to
discourage Centres from receiving funding from commercial sources because they
are the public face of the Collaboration.
Jim explained that the Steering Group had been split on this issue, but
it was thought that there could be circumstances in which commercial funding
might be acceptable for certain activities such as translation (particularly
translation of The Cochrane Library
into Spanish) and methodological work.
It was restated that review production remains insupportable from
commercial funds. Kay Dickersin, US
Cochrane Center, submitted a motion that the Steering Group should reconsider
the issue of commercial funding, as defined in its existing policy document for
all entities other than CRGs. The
motion was carried by majority vote of the entity representatives.
9.2.3 Discussion on 4 October 2004: Following
discussions at the Annual General Meeting on 3 October, at which a number of
people had strongly disagreed with the new policy for Centres, and a motion had
been carried for the Steering Group to reconsider, they revisited the subject
at their meeting on 4 October. There
was unanimous support for Jordi, and distress at the nature of some of the
comments made during the Annual General Meetings about the conduct of the
survey. Sally undertook to explain at
the Centre staff meeting on 5 October that the survey had been devised by all
four Centre representatives, and was not flawed in any way, and also to e-mail
all Centres to this effect after the Colloquium. It was agreed that this issue should be discussed again at the
next Steering Group meeting in Providence in April 2005. In the meantime, Centres can continue to
accept commercial funding for activities unrelated to review production, as
that was the case before this meeting.
At the Providence meeting, particular consideration should be given to
the impact of policy decisions on people in non-English-speaking and developing
countries. It may be that the focus
should be on activities rather than type of entity. The funding of translations is an important consideration, as is
the credibility of The Cochrane Collaboration.
Jim undertook to draft a document with help from Jon, Liz, Rob and
Sally, to circulate to the Steering Group, and then to send to all entities,
describing why the Steering Group had found it extremely difficult to come to a
decision, including various policy options, and providing a framework for
feedback.
Action: Jim, Jon, Liz, Rob, Sally
9.3 Central fund or foundation for
receiving unrestricted donations: It was agreed to defer this discussion until the
Steering Group meeting in Providence.
In the meantime, Nick was asked to circulate his proposal to all
entities for their feedback, to inform the discussion in Providence.
Action: Nick
10. Report
from Wiley representatives
Mike explained that the main issue
for the Steering Group was whether or not to give Wiley permission to give
three months’ notice to Update Software to turn off their site, and for the
Internet version of The Cochrane Library to be available solely on the
Wiley InterScience (WIS) site. It was
agreed that there were no outstanding questions in relation to the analysis and
display of the statistical results of Cochrane reviews, or to the current ‘look
and feel’ of the product, and that the items that still need to be fixed are
all to do with searching The Cochrane Library. With regard to the Comments and Criticisms system, the Steering
Group is satisfied that Wiley is developing an appropriate solution in
consultation with the Criticism Management Advisory Group. Wiley should be asked to provide more detail
on their mechanism for continuous quality improvement, and the importance of
this process should be stressed to them.
They should also be asked to provide their strategic future plans for
making the product more accessible to clinicians, people from developing
countries, consumers, and other users.
Carol Lefebvre (UKCC), and Deborah Dixon and Deborah Pentesco-Gilbert (John
Wiley and Sons) joined the meeting at this point. Carol was asked to summarise the searching difficulties on the
WIS test site. She reported that the
biggest difficulty had been the timing out during searching, which had resulted
in a limited amount and extent of testing taking place to date. (She confirmed that the Search Testing Group
is content with the solution proposed by Wiley to resolve the timing out difficulty.) She noted that the Search Testing Group
still needs to finish the testing of searches for authors/reviewers and
editorial bases. She outlined that the
Group could resume their testing on 19 October with the new release of The
Cochrane Library, and that it would be able to report next to the Steering
Group on 24 November. Deborah PG said
that Wiley is grateful for the good working relationship it has had with the
Search Testing Group. Deborah D said
that Wiley is willing to continue to pay Kate Light for her search testing
work. Davina pointed out that it is
normal for software to go through a continuous process of identifying errors,
which are then resolved. Deborah D
stressed that it is in everyone’s interests to have a continual process for improving
The Cochrane Library. She explained
the importance of the Steering Group’s decision in relation to subscribers
wishing to take out subscriptions to WIS from the beginning of 2005. There has been a lot of confusion among
potential customers about the two sites (Wiley and Update Software). Deborah PG said that training sessions are
underway in the southern hemisphere but a final product is needed to make this
effective. Lisa thanked Wiley for its
work in the USA which has hugely raised the profile of The Cochrane Library,
and was reassured by Deborah PG that the Comments and Criticisms system
will be public by Issue 1, 2005. Once
the Steering Group gives permission to Wiley to give three months’ notice to
Update Software, four weeks would be needed in order to complete the transition
to the Wiley InterScience site in those countries with national provision. Carol, Deborah D and Deborah PG left the
meeting at this point.
After further detailed discussion, there was unanimous agreement for Nick to
tell Wiley that it has the Steering Group’s permission to issue three months’
notice to Update Software. On behalf of
the Trading Company directors, Monica reported satisfaction with this
decision. Mike undertook to let Carol
know of this decision before Nick informs Wiley, and to restate the gratitude
of the Steering Group for the hard work done by the Search Testing Group.
Action: Mike, Nick
Nick was asked to stress to Wiley that one of the reasons that they are
being given permission is because the Update Software CD-ROM version will continue
to be available as back-up. It was
agreed that the Wiley version of the CD-ROM should be tested extensively before
Wiley is given permission to withdraw the Update Software version. The Trials Search Co-ordinators (TSCs)
should be closely involved in testing the CD-ROM version, and Davina was asked
to convey this to the TSCs during the Colloquium. Mike reported that the Search Testing Group is willing to
continue testing, and will work with Wiley to an appropriate timescale.
Action: Nick, Davina
4 October: Deborah D and Deborah PG
attended the second Steering Group meeting to complete the discussion of their
report. Deborah D explained that she
had asked the Institute for Scientific Information (ISI) for a detailed
specification that would enable ISI to capture the citations of Cochrane
reviews. Wiley was asked to give the
Collaboration some guidance on the issue of the number of reprints that would
constitute a bulk sale. Nick asked how
the pay-per-view system would work, linking directly to the full Cochrane
review on Wiley InterScience, and Deborah D said she would follow up on this
and let him know.
Deborah D requested clarification from the Steering Group of the approval
process for the CD-ROM version of The Cochrane Library. Update Software’s initial reaction had been
to request early notice (by the end of October 2004) that they would still be
required to produce the CD-ROM version for Issue 2, 2005, and Wiley needed to
agree the notice period with Update Software (which should be a maximum of
three months). She asked if a process
could be agreed: the Steering Group
needs to be happy with the product once all major search testing strategies
have been tested and found to be satisfactory on the Wiley version of the
CD-ROM. Deborah PG described the
testing of the CD-ROM that had already been done. Online statistical analysis software and the ‘look and feel’ are
the same on the CD-ROM as on the Internet version. Jon said that the Statistical Testing Group would still like to
see the CD-ROM to test that nothing has changed, and Sally pointed out that the
testing process should be the same for the CD-ROM as for the Internet
version. The Search Testing Group
should be asked to document what they test on the Internet version, so that the
scripts can be used when testing the CD-ROM version. The Steering Group, the Publishing Policy Group, and Trials
Search Co-ordinators should all be provided with the CD-ROM in order to provide
their feedback, and Wiley will provide a timescale for this. The whole Steering Group should be consulted,
and should be confident that the Wiley version of the CD-ROM is as good as the
Update Software version before retiring the Update Software version; this will
not necessarily be completed by the end of October 2004.
Action: Deborah D and Deborah PG
11.
Methodological
quality improvement projects
Mike declared a conflict of interest
and left the room for discussion of this item, which Jim chaired. Jon presented details of seven projects
that had been proposed by the Convenors of Methods Groups, the Handbook
Advisory Group and the Quality Advisory Group, to improve the methodological
quality of Cochrane reviews:
Project 1: Obtaining a consensus
on a strategy for assessing trial quality (protection from bias) for Cochrane
reviews: This was considered to be the
top priority, and should be funded.
Project 2: Improving the quality
of analyses of time-to-event data in Cochrane reviews: This was also considered to be important,
but of lower priority, and should be funded.
Project 3: Obtaining a consensus
on the content and methods of a ‘Summary of Findings’ table (balance sheet) for
Cochrane reviews: This was considered a
high priority, as it impacts on RevMan 5, and should be funded.
Project 4: Involvement of
Cochrane methodologists in revision of the statement of standards for reporting
for systematic reviews (QUORUM): This
was considered important and should be supported. However, Jon should send a revised costing to the Executive for
approval, to fund only one person (who should be a member of the Handbook
Advisory Group) to attend the QUORUM meeting to represent The Cochrane
Collaboration.
Project 5: Development of tools
to educate and assist authors/reviewers dealing with cross-over, cluster randomised,
change-from-baseline and other non-standard trial designs: This was also considered important and
worthy of funding. A statistician will
need to be identified for the project.
Project 6: Development of a
surveillance program of the methodological quality of Cochrane reviews: This was agreed not to be a priority to fund
at the present time.
Project 7: Identification and
evaluation of interactive software to help Cochrane authors/reviewers improve
the quality of their reviews: This was
of lower priority and should not be funded at the present time.
The total budget agreed was £36,485 for Projects 1, 2, 3 and 5, plus the
revised costs of Project 4. Thanks were
expressed to the methodologists for preparing these project proposals. Additional project proposals should be
brought to the mid-year Steering Group meeting in Khon Kaen, Thailand, in
2006.
Action: Jon
12.
Creation of
umbrella (summary) reviews
Jon explained the background to this
issue, which had been under discussion for a couple of years. He stressed its importance, as it may result
in a new style of review. He said that
CRGs are working in an unco-ordinated way, and asked for approval to spend
£1,800 to enable the working party to hold several telephone conferences. He said he was unable to continue to convene
the working group, but would be happy to continue to be involved. Lorne Becker was invited to join the working
group to represent Fields, and his offer to take over from Jon as convenor was
accepted.
Action: Lorne
13.
Prioritisation of
key topic reviews
Jim explained that the issue of
prioritisation of key topic reviews had arisen at the Funders’ Forum. He also reported another conversation during
the Ottawa Colloquium about the Collaboration having arguably lost an
opportunity to make important global impact by not having anti-retroviral drug
reviews available at the critical time for policy makers. Sally advised that there would be a plenary
on usability and relevance issues during the Melbourne Colloquium, and invited
Steering Group members to let her know if they wished to participate in that
plenary. Liz said it was important to
look at methodological issues in relation to priority setting, and in
particular how The Cochrane Collaboration keeps abreast of the issues facing
organisations like WHO, for example, global social determinants of health; this
will require attention to methods for reviews that provide an evidence base for
these sorts of questions. Liz and Peter
agreed to prepare a paper for discussion at the next Steering Group meeting in
Providence on the issue of strategic directions for review topics, and whether
the Collaboration structure as it stands could accommodate some of the more
pressing issues such as social determinants.
Action: Liz, Peter
14.
Developing
countries initiative
Jim undertook to write to Joy Oliver
at the South African Cochrane Centre to thank her for the survey she had
conducted recently of members of the Collaboration based in developing
countries. He would ask her for an
analysis of the survey results for discussion at the next Steering Group
meeting in Providence.
Action: Jim
15.
Verbal reports
from outgoing Steering Group members
The outgoing members of the Steering
Group gave verbal reports about their experience as members of the Group. Silvana spoke about
how she had been enriched by the experience, and asked for consumers to remain
a focus. Gerd said that the whole
system had become more efficient, although he worried about concentrating too
much on process; he felt it had been a privilege to contribute as a member of
the Steering Group. David said how much
he had enjoyed working on the Steering Group, and echoed Gerd in appreciating
the improvements that he had observed over the past three years; he drew attention
to the fact that there would be less clinical input to the Steering Group on
his leaving it. Mike said that the past
two Steering Group meetings had been the most difficult for him, but that he
had learnt much from his whole time on the Steering Group; he said that the
Steering Group should not be afraid to change things. Jim thanked the four outgoing members on behalf of the whole
Group for their hard work and many contributions.
16.
Future membership
of Steering Group sub- and advisory groups
A table of proposed sub- and advisory
group membership was circulated at this point in the meeting. Mike explained that the proposed
assignment of Steering Group members to particular groups was open to
discussion. All Steering Group members
(with the exception of the Co-Chairs) should ideally be on no more than one
sub-group, and advisory groups should each have two Steering Group members on
them. People were invited to speak to
Jim or Kathie before the next meeting on 4 October if they wished to contribute
to a different sub-group than that to which they had provisionally been
allocated. No-one asked the Co-Chairs
if they could be reallocated to a different group, and Jini should therefore
arrange for the membership lists and e-mail discussion lists to be updated as
soon as possible.
Action: Jini
17.
Relationship with
Guidelines International Network (G.I.N.)
Jim had prepared a paper about the
work of G.I.N. and how it complemented the work of The Cochrane
Collaboration. It was agreed that
discussions should continue about formalising a working relationship between
the two organisations. Jim agreed to
draft a Memorandum of Understanding between The Cochrane Collaboration and
G.I.N. with the help of Rob and Sally.
Kathie suggested the need to establish criteria upon which to base
future decisions as to which partnerships/endorsements the Collaboration would
enter into, and offered to work on a document outlining the criteria and a
reporting process, for discussion at the next Steering Group meeting in
Providence.
Action: Jim, Rob, Sally, Kathie
18.
Relationship with BMJ/Clinical Evidence
Jon said that Mike Clarke had undertaken to continue to be the
liaison person between The Cochrane Collaboration and BMJ/Clinical
Evidence. In response to a question
about the exclusivity of the Cochrane-Wiley book series, Nick clarified his
recommendation that anybody who is producing a book based on Cochrane reviews
should first consider approaching Wiley to publish it, but stressed that this
is not an exclusive arrangement. (See
also item 5.1 above.)
19.
Endorsement of
the CONSORT Statement
Jon explained that the CONSORT
Statement provides a method of improving the reporting of randomised controlled
trials which has been widely adopted by medical journals, and has already made
a difference to the quality of reporting of trials. Many members of The Cochrane Collaboration had been involved in
its development. It is an initiative of importance to authors of
systematic reviews and hence to the Collaboration. On this basis, Jon
proposed that the request for endorsement should be accepted by the
Collaboration. He also pointed out that
in order to organise its meetings the CONSORT group had needed to obtain
funding from multiple sources, including pharmaceutical companies (as is
declared in their published statements).
He noted that this was unfortunate but typical of methodological
developments. It was pointed out that the Steering Group discussions of
conflict of interest had related only to the Collaboration's activities and not
to those of other groups, and that this should not be a reason to stop the
Collaboration from endorsing the work of others, if merited. It was
agreed to endorse the CONSORT statement, and Jim agreed to write to Doug
Altman, David Moher and Ken Schulz who had requested this endorsement.
Action: Jim
20.
Relationship with the James Lind Alliance
The Steering Group agreed that it should support this
important initiative. Jim agreed to
write and wish Iain Chalmers well, and to suggest that the UKCC be represented
at the meeting on 1 December 2004, and that a Cochrane Consumer Network
representative also be invited to attend.
Action: Jim
21.
Agenda and format
of the Annual General Meetings
It was agreed to add two items to the agenda of these meetings: the Steering Group’s agreement at this
meeting to give John Wiley and Sons permission to give Update Software three
months’ notice in relation to the Internet version of The Cochrane Library,
and the issue of commercial sponsorship to Centres. An explanation about the large amounts of funding committed to
certain projects should be raised under the Treasurer’s report, to allay
concerns that the Collaboration appears to have large cash reserves.
Action: Jim, Mike
22.
Reports to the
Steering Group:
22.1 Monitoring and Registration Group:
Sally thanked Claire for the
excellent support she provides to this Group.
She also expressed thanks to Kathie for her enormous contribution to the
MRG while she was Co-Convenor. Jim said
that the MRG report was very well presented.
Kathie will chair a working group reporting to the MRG to assess the
current coverage of entities in the Collaboration to guide assessment of the
need for future entities seeking registration.
The working group will look at both global coverage (with respect to the
need for additional Centres) and clinical coverage (with respect to the need
for additional CRGs and Fields).
Entities are monitored against core functions, not against whether they
have adhered to the registration criteria (which include core functions but
extend beyond them). Davina asked
whether those criteria could be revisited with a view to incorporating them
into the monitoring system. Sally asked
whether one of the Co-Convenors of the MRG could in the future be a non-member
of the Steering Group, and this was approved, as long as that person has served
one year on the MRG beforehand. This
decision should be reflected in the document entitled ‘Structure, remit and
membership of groups accountable to the Steering Group’ on the website.
Action: Jini
Sally reported that the MRG would in future write a short report for each
entity representative to distribute, about issues of importance in their area
of responsibility. The key findings
from the 2003 round of monitoring were presented. Funding was the single biggest cause for concern among specific
entities. The MRG will work with the
CRG and Field representatives on the Steering Group to develop closer working
relationships. The Steering Group
agreed to the establishment of a formal working group to look at updating
reviews; central data inputting was proposed as a potential way to relieve this
problem to some extent. Rob agreed to
take the lead on this, with assistance from Davina, Mark and Jessie McGowan,
and report to the next Steering Group meeting in Providence. Public access to MRG reports to the Steering
Group was endorsed, keeping the identity of individual entities
confidential. It was noted that RGCs
need more support. Monica pointed out
that the members of IMS Support are in the process of contacting all RGCs to
discuss issues around the IMS; in doing so, they are also trying to help
address non-software issues. Davina
reported from the RGCs’/TSCs’ meeting on the poor relationship between some
RGCs and their Co-ordinating Editors, and the lack of support that RGCs feel
from their Co-ordinating Editor. Peter
said that he would address this with the Co-ordinating Editors, and it was
agreed that the need for support for RGCs should be revisited in
Providence. It was noted that there is
now much stronger Field representation on the MRG. Zbys had invited the MRG to hold their mid-year meeting in
Bahrain, with a view to providing input to local seminars while there, and the
MRG is considering this.
Action: Sally, Steff, Rob, Davina,
Mark, Peter
22.1.1 Frequency of monitoring: Sally
presented the case for entities to be monitored once every two years instead of
annually. They would still be asked to
provide Part B on funding on an annual basis (to the Secretariat). There was approval to try this new schedule,
starting with the January-December 2004 monitoring round, and with a formal
evaluation during January-December 2007.
Action: Sally, Steff
22.1.2 Revision of section on Centres in
The Cochrane Manual: The proposed
revisions to the section on Centres were agreed to, with one small
clarification; Jini was asked to make the necessary changes in the Manual.
Action: Jini
22.2.1 Monitoring
the Steering Group: Peter agreed to work with the Co-Chairs of the
Steering Group and Janet to draft clear terms of reference and a timeframe, and
a shortlist of people who might be involved.
This will be discussed at the next Steering Group meeting in Providence.
Action: Peter, Jim, Kathie, Janet
22.2.2 Procedure for
selecting a Chair of the Steering Group:
Peter asked for clarification of how the proposed procedure for
selecting a new Chair/Co-Chair would work.
It was agreed that in future there should be a formal process of
nominating and seconding, and the members of the Steering Group would
vote. Nominations should be made nine
months in advance and discussed at the mid-year Steering Group meeting. If no
member of the Steering Group comes forward for selection, or if the person
or people who come(s) forward are judged unsuitable by the Steering Group (by
vote if necessary), a person from outside the Steering Group would be sought. Monica proposed that this should happen six
months before the position of Co-Chair becomes vacant, Peter supported this
proposal, and it was agreed. It was agreed that candidates should provide a brief written description
of their credentials for taking on this responsibility. This description of the agreed procedure for
selecting a new Chair/Co-Chair should be confirmed via e-mail to the Steering
Group.
Action: Jim
22.2.3 Steering Group elections: information on candidates: It was
agreed that Phil Alderson’s suggestion to change from candidates providing a
200-word summary to something more structured (i.e. a series of questions
covering the candidate’s background, abilities, and views on topical issues),
should be adopted. Jon volunteered to
ask Phil if he would develop a template for this, and circulate it to the
Steering Group for approval.
Action: Jon
22.3 Cochrane CENTRAL Advisory Group
(CCAG): Jim undertook to write and thank Kay Dickersin for her
report on behalf of the CCAG. Davina
agreed to bring a formal proposal to the next Executive teleconference for
approval of a continuing budget for MEDLINE retagging. She was also asked to find out from the CCAG
who the Handbook Advisory Group should liaise with in regard to Section 5 of
the Cochrane Reviewers’ Handbook, since it was agreed that the CCAG and HAG
have joint responsibility for this section.
Davina also agreed to clarify in writing the situation with regard to
Kay’s and the CCAG's understanding about the integration of CENTRAL and
specialised registers into the new IMS.
It was pointed out that the Steering Group had not come to a decision at
their Bergamo meeting in March 2004 about whether or not this should happen,
nor whether CRGs would be required to enter and edit records in their
specialised registers or in CENTRAL online; instead, the Steering Group had
asked the IMSG to form a subgroup which would make recommendations on the
desirability and feasibility of doing this.
Action: Jim,
Davina, Mike, Monica
22.4 Cochrane Library Users’ Group (CLUG): Kathie
reported that she could not yet confirm who the new Convenor of CLUG would be,
but thought this might be resolved during or shortly after the current
Colloquium. She agreed to keep the
Steering Group informed of developments.
Post hoc note: Emma Irvin,
librarian at the Institute for Work and Health in Toronto, Ontario, Canada,
volunteered to take on this role, and the Steering Group approved this
appointment.
22.5 Colloquium Policy Advisory Group
(CPAG): Jim undertook to write and thank Claire Glenton and
Alessandro Liberati for their report.
Alessandro had recently resigned as Co-Convenor, and Jim was asked to
thank him for his valuable contribution in this role.
Action: Jim
Post hoc note: Steve McDonald of the Australasian Cochrane
Centre volunteered to take on this role, and the Steering Group approved this
appointment.
22.6 Criticism Management Advisory Group
(CMAG): Jim undertook to write and thank Sherri Sheinfeld
Gorin for her report on behalf of the CMAG.
It was agreed that the membership of this Group needs to be
revisited. Monica suggested that all
Advisory Group Convenors should be asked to revisit the remit of their group,
as it is difficult to persuade someone to join an advisory group without
providing a detailed remit. Lisa agreed
to raise this with the CMAG, and Nick to bear this in mind when resuming his
task of revisiting the remits and memberships of the advisory groups.
Action: Jim, Lisa, Nick
22.7 Handbook Advisory Group (HAG): Jim
thanked Sally for the report from the HAG.
He said he would also write and thank her Co-Convenors, Phil Alderson
and Julian Higgins, and encourage them to apply for funding for the next
financial year, as all advisory groups will be encouraged to do. Endorsement was given to the proposed
changes in remit and membership. The
remit of the HAG now includes providing advice to the RevMan Advisory Group and
the Steering Group on the content and structure of Cochrane reviews (in
particular by gathering opinion from Methods Groups), and providing advice on
structure style and production to the editors of the Cochrane Handbook for
Diagnostic Test Reviews. The membership
will include the Co-Convenors of the HAG; one named Convenor from each Methods
Group, the Adverse Events Sub-Group, and the Methodology Review Group; those
methodologists currently on the editorial board without a role as a Methods
Group Convenor; at least one RGC, TSC, Co-ordinating Editor, Author/Reviewer,
and Field Convenor; and two members of the Steering Group. These changes should be reflected in the
document, ‘The structure, remit and membership of groups accountable to the
Steering Group’ on the website. The
Co-Convenors were asked to be explicit in future about the remit and membership
of HAG’s editorial board. Liz stressed
the importance of ensuring Field representation on the HAG, as there are many
diverse methodological issues identified and worked on by members of
Fields. The proposed change of name of
the ‘Cochrane Reviewers’ Handbook’ to the ‘Cochrane Handbook for Systematic
Reviews of Interventions’ was approved.
Jon reported that the Cochrane Handbook for Diagnostic Test Reviews is
already in preparation, and its editors will liaise with the editors of the
Interventions Handbook to avoid unnecessary duplication of effort.
Action: Jim, Sally, Jini
22.8 Information Management System Group
(IMSG): Jim undertook to write and thank Mike for his report
as Convenor of the IMS. The Steering
Group supported the establishment of a sub-group of the IMSG to deal with issues
pertaining to the Contact Database.
Action: Jim
22.8.1 Suggested amendment to terms of use of the
Contact Database: The Steering Group agreed with the decision that had
been made by the Executive on 21 June 2004, to amend the terms of use of the
Contact Database, to allow people within the Collaboration to use the
information it contains in certain circumstances, with permission from the
Executive. Until now, the default
option in the Contact Database with regard to bulk mailings has been ‘None’
(i.e. I do not wish to receive any bulk mailings). Monica recommended that the default, in phase 1 of the new IMS,
should be changed to ‘I wish to receive mailings from my primary entity only’. She was asked to consider whether a pick
list of all entities could be provided in the Contact Database under the new
IMS, so that one could indicate the entity/entities from whom one does
want to receive mailings.
Action: Monica
22.9 Quality Advisory Group (QAG): Jim
thanked Sally and Phil Alderson for their report. Sally advised that the Executive would be receiving a report and
a request for ongoing funding from the Style Guide Working Group shortly after
this meeting. She said that the QAG
Convenors felt strongly that it should be a central responsibility to maintain
the Style Guide, with an associated budget, and this was agreed. Jim asked Sally to pass on thanks to Sarah
Hetrick for the work she had done in making the resources identified by Nancy
Owens as Quality Improvement Manager available to CRGs on the website. It was agreed that ongoing support for this
project had Steering Group approval.
Liz raised concern that Sally is Co-Convenor of the MRG, QAG and HAG, as
this is a heavy workload. Sally pointed
out that she has Co-Convenors who share the workload but, in the case of QAG
and HAG, her Co-Convenors were not at the Steering Group meeting to
report. It was agreed that it is
important to guard against any Steering Group member being overloaded. Davina asked whether central copy editing should
be mandatory. The current process is
somewhat cumbersome, so this could be considered in the longer term, at the
time of the Steering Group meeting in Melbourne in October 2005. Monica reminded Advisory Group Convenors
that the members of their advisory group should have this role assigned to them
in the Contact Database, so that people can access this information.
Action: Sally
22.10 Cochrane reviews of diagnostic test accuracy
working group: Jon reported that development of specifications for
the software for these types of reviews is already under way. Materials will be piloted with a few CRGs in
2005, with the aim of releasing the Handbook for Diagnostic Test Reviews during
the Melbourne Colloquium. The key
concern is to find support for CRGs, and a model is proposed of having four
regional support centres located where methodologists are working already,
associated with Australasian, Dutch, UK and US entities. He said he had been talking to funders and
was optimistic. It was re-emphasised
that there was no expectation that CRGs would take on this additional workload
without additional resources. The
development plan was endorsed by the Steering Group, and Jon’s request for
additional funding was approved. Monica
was hopeful that it might be possible for the software for the special version
of RevMan to be developed within the existing IMS budget, but until the
specifications had been finalised and reviewed this was uncertain.
22.11 The Ombudsmen: Jini was asked to pass
on thanks from the Steering Group to Gill Gyte and Peter Langhorne for their
report. She was also asked to find out
from Gill whether she had been in contact with the author/reviewer mentioned
under item 2004/04 of the report, and to ask her to clarify whether this had
been taken in the first instance to the Director of the reference Cochrane
Centre.
Action: Jini
22.12 The Publication Arbiter: David
Henderson-Smart and Kay Dickersin attended the second Steering Group meeting on
4 October, for this item only. Jim thanked
them for their report, which David said had been difficult to anonymise. Davina left the meeting for the discussion
about one review for which she was conflicted, and Janet asked for consumer
input to be obtained for this review.
Kay Dickersin agreed to become Co-Publication Arbiter with David. Jini should update the website and the
Steering Group module accordingly.
Action: Jini
22.13 The
Funding Arbiter: Jim thanked Mark for his report. It was agreed that the Funding Arbiter
must be a member of the Steering Group, and at least one of the panel members
must not be a member of the Steering Group; the third panel member may or may
not be a member of the Steering Group.
Approval was given for Mark to go to a third person in circumstances in
which one member of the Funding Arbitration Panel is unable to participate (for
example, due to a conflict of interest); if the two remaining Panel members are
unable to reach consensus, the Co-Chairs of the Steering Group will be asked to
nominate a third person to join the Panel temporarily. This person could be a member of the
Steering Group, one of the Co-Chairs, or a member of the Collaboration who is
not a member of the Steering Group. It
was agreed that the term of the Funding Arbiter should be limited by their term
on the Steering Group (i.e. three years, with the possibility of another
three-year term if re-elected). The
term for the other panel members should also be three years, again with the
possibility of a second three-year term.
No two panel members should leave the panel at the same time or within
twelve months of each other, i.e. panel membership should be staggered so that
there is continuity within the panel.
It was also agreed that appeals against decisions made by the Funding
Arbiter should go to the Steering Group.
The administrator of the Australasian Cochrane Centre should continue to
provide support to the Funding Arbiter, with the Secretariat providing support
only if a situation arises which would put the ACC administrator in a position
of conflict. Jini should update the
Collaboration website and the Steering Group module accordingly.
Action: Jini
22.14 The Funders’ Forum: Dan Fox attended the meeting for this item only, and
reported that the Forum provides the opportunity for people who can be or are
already in the external constituency to meet with leaders of the
Collaboration. He reported that people
from nine countries would attend the Forum meeting on 2 October. He explained that the Forum began formally
at the Cape Town Colloquium four years ago, had met at every Colloquium since
then, and is evolving with each meeting.
Dan emphasized the uniqueness of the Funders’ Forum: he said he did not know of any other
scientific organisation in the world that had forged such a close and
satisfactory relationship with its actual and potential funders. He described an initiative to bring The
Cochrane Collaboration to the attention of the media, particularly in the
United States. Mike explained that
items would be brought from the Forum to the Steering Group for
discussion. Peter thanked Dan for his
energetic involvement in this initiative.
Dan explained the challenge of persuading people to join the Forum, and
asked Steering Group members to inspire people in their own country to
participate; he emphasized that the single most important goal is to raise the
profile of the Collaboration in the countries of members of the Forum. Lisa thanked Dan for his role in turning the
USCC advisory board into a more active group.
She asked if ways could be found for communicating better between
meetings to take this initiative forward.
Mike asked the Steering Group to think about involving Dan more in their
discussions in future.
At the second Steering Group meeting on 4 October, Nick reported back from the
meeting of the Funders’ Forum held on 2 October. Two major issues that had been discussed were the prioritisation
of key topic reviews, and the possibility of attracting funding for specific reviews. Jim said that Dan Fox would be trying to
co-ordinate several meetings during the coming year, the outcome of which would
be crucial to the continuance of the Forum.
One of these would be specifically to bring together potential funders
for reviews of diagnostic test accuracy.
22.15 Cochrane-Campbell liaison: Jim welcomed Haluk Soydan, Co-Chair of The Campbell
Collaboration with Bob Boruch, to the meeting.
Haluk thanked Kathie and Peter for their helpful contributions to
Campbell Collaboration Steering Group discussions. He said that advice from the Cochrane Consumer Network would be
appreciated.
Action: Janet
23.1 Co-Chairs: Kathie volunteered to draft a sentence
to add to this job description, to reflect the fact that the Co-Chairs are the
official spokespersons for the Collaboration.
Sally asked Jim to include a statement as to the minimum time commitment
needed from the Co-Chairs. After these
two amendments have been made, this job description should be included in The
Cochrane Manual.
Action: Kathie, Jim, Jini
23.2 Steering Group members: It was agreed to defer discussion of this
job description to the next Steering Group meeting in Providence due to lack of
time, when the difficulties experienced by the two CRG ‘at large’
representatives in defining their constituency should also be addressed.
Action: Jini
23.3 Publication Arbiter:
It was agreed to defer discussion of this job description to the
next Steering Group meeting in Providence due to lack of time.
Action: Jini
23.4 Funding Arbiter: It
was agreed to defer discussion of this job description to the next Steering
Group meeting in Providence due to lack of time. It was noted that information contained in the document prepared
by Mark, outlining the role and processes of the Funding Arbiter, should be
added to the Collaboration website and the Cochrane Manual.
Action: Jini
23.5 Ombudsmen: Gill Gyte and
Peter Langhorne are currently preparing a draft job description for the
Ombudsmen. Jini was asked to let them know
that this would be put on the agenda of the Steering Group’s next meeting in
Providence.
Action: Jini
23.6 Company Secretary: The
text of this job description had been taken from material provided by Companies
House in the UK. The Executive had approved
its content in late July, and it had already been included in The Cochrane
Manual. It was included with this
agenda in case it needed to be referred to in the light of the several draft
job descriptions above.
25.1 Collaborative Review Group
issues:
25.1.1 Gender balance of Editors: The Steering
Group noted with interest the paper prepared by Paul Garner and Paula Waugh of
the Cochrane Infectious Diseases Group, on the distribution of editors of
Collaborative Review Groups by gender.
Jim would write and thank them for this. The CRG representatives on the Steering Group agreed to try to
encourage CRG editorial teams to involve more women as editors.
Action: Jim, Davina, Mark, Peter,
Steff, Zbys
25.1.2 Non-randomised
studies and specialised registers: Davina
requested that this item be deferred to the next Steering Group meeting in
Providence, and agreed to ask the Non-Randomised Studies Methods Group to
contribute to a paper for that discussion.
Action: Davina
25.1.3 Filming of Colloquia
sessions: Davina asked whether it
would be feasible for certain sessions at the Colloquium to be filmed and made
available on the website to people who were unable to attend in person. Sally undertook to investigate this for the
Melbourne Colloquium.
Action: Sally
25.2 Methods Group issues: Jon
had no further issues to raise.
25.3 Field/Network
issues: Liz had no further issues
to raise. Jim said that the
re-energised Field representation on the Steering Group was most welcome.
25.4 Centre issues: Lisa reported that the
Centre Directors had asked for information on the funding of each Centre, and
Nick was asked to seek clarification of their request.
Action: Nick
25.5 Consumer Network: Janet
reported that the Consumer Network as a legal entity is in the process of being
de-registered, and a new Network is being constituted. Their revised website material would shortly
be ready to go public on cochrane.org.
27.1 Providence: 2-4 April 2005 (mid-year):
Nothing additional to discuss.
27.2 Melbourne: 21
& 24 October 2005: Nothing to
discuss.
27.3 Location
in 2006 (mid-year): Jim said that
the Steering Group had received three invitations for this meeting, from
Chengdu, China; Copenhagen, Denmark; and Khon Kaen, Thailand. Sally declared a conflict of interest in
relation to the Thai Cochrane Network.
Jim agreed to write to Pisake Lumbiganon to accept the invitation of the
Thai Cochrane Network. He would also
write to Youping Li and Peter Gøtzsche to thank them for their invitations,
which would go into the pool for discussion at the Providence meeting in
relation to subsequent Steering Group meetings.
Action: Jim, Jini
27.4 Dublin, in October 2006: Nothing to discuss.
27.5 Location
in 2007 (mid-year): Calls should be
made to all Centres in future, inviting offers to host the mid-year meetings
and Colloquia.
28. The next three Cochrane Colloquia:
28.1 Melbourne, Australia, 22-26 October 2005: A progress
report was presented in the background papers, for information. There was nothing to discuss in
relation to next year’s Colloquium.
28.2 Dublin, Ireland, October 2006: There was
nothing to discuss in relation to the 2006 Colloquium.
28.3 São Paulo, Brazil, 2007: Jini
was asked to help the Brazilian Cochrane Centre in scheduling the dates for the
2007 Colloquium, to avoid clashing with major national public holidays, notably
Canadian Thanksgiving and Yom Kippur.
Action: Jini
28.4 Proposal for development of ‘Colloquium
Manager’: It was agreed that the software that had been developed
at the Norwegian branch of the Nordic Cochrane Centre was extremely useful, and
its development should be supported centrally for the benefit of future
Colloquium organisers. Jini was asked
to let Shaun Treweek know that his request for funds to provide two months of
programmer time, server hosting, licensing and e-mail, was approved, to a
maximum of 85,000 Norwegian Krone (approximately £7,000 sterling), and that he
should arrange for an invoice to be sent to her. The need for further expenditure on development should be
reviewed annually.
Action: Jini
DECLARATIONS OF INTERESTS OF STEERING GROUP MEMBERS, IMS DIRECTOR, AND SECRETARIAT STAFF
GODWIN
AJA, Consumer Network Representative,
Cochrane Collaboration Steering Group (from 3 October 2004):
Godwin
Aja has no conflicts of interest to declare.
GERD
ANTES, Centre Representative,
Cochrane Collaboration Steering Group, Member of Publishing Policy Group, and
Steering Group representative on Information Management System Group (until 3
October 2004); Director, German Cochrane Centre:
Gerd
Antes is employed by the University Hospital, Freiburg, as Director of the
German Cochrane Centre. This contract is not limited in the sense that the
employment will last until his retirement, but the position can be changed by
the employer. The University Hospital Freiburg is his source of regular income.
In addition he has received and receives payment for speaking and for writing
from some journals and from some organisations, including manufacturers of
health care products. All payments are on a one-off basis and there are no
regular or long-lasting personal relationships with any organisation. Gerd
Antes is Chair of the Advisory Board of 'Current Controlled Trials', and
receives an annual retainer and travel expenses for this work. The German
Cochrane Centre has been and is supported by manufacturers of health care
products, health insurances and a large hospital association to conduct
projects and to organize meetings and conferences. Gerd Antes has played a
central role in setting up the German Network for Evidence-Based Medicine and
is now co-chair of the Network. This not-for-profit organisation has 28
supporting organisations, across all stakeholders of the German health care
system, including pharmaceutical companies. The network is heavily dependent on
this support and could not offer some services without this support. In
particular, the network offers the lowest priced access to The Cochrane
Library in Germany to its members. There are no financial links to
manufacturers of health care products or other stakeholders of the health care
system. He does not believe that any religious, political or other beliefs he
may hold have a strong biasing influence on any of his work.
LORNE
BECKER, Co-ordinator, Primary Health
Care Field; Author/Reviewer and Peer Referee, Acute Respiratory Infections
Group; Author/Reviewer, Tobacco Addiction Group; Member, Drugs and Alcohol
Group and Pain, Palliative and Supportive Care Group:
Lorne
Becker is Emeritus Professor in the Department of Family Medicine at SUNY
Upstate Medical University, having recently retired from his position as
Professor and Chair of that department.
He has received and continues to receive honoraria for speaking
engagements - usually on topics related to the application of evidence in
clinical practice by primary care physicians. He serves as the Evidence Based
Medicine Editor for the electronic publication 'DiseaseDex', and receives an
annual honorarium from Thomson Micromedex for this activity. He serves periodically as a remunerated
expert for the New York State Office of Professional Medical Conduct and in
some legal cases. He is an associate editor for the Journal of Family Practice
and a member of the board of the Family Physicians' Inquiries Network, and
receives no compensation for either of these roles.
LISA
BERO, Centre Representative, Cochrane
Collaboration Steering Group (from 3 October 2004); Member, Cochrane Effective
Practice and Organisation of Care Group:
Lisa
Bero has been a full-time faculty employee of the University of California, San
Francisco, since 1991. Her salary is
provided by funds from the state of California and her research grants. She has had or currently has research grant
funding from the National Institutes of Health, American Cancer Society, Robert
Wood Johnson Foundation, Agency for Healthcare Research and Quality (AHRQ),
World Health Organization, and California Tobacco-Related Disease Research
Program (research money derived from the tax on cigarettes). Dr Bero receives about $50.00 US per year in
royalty fees for the publication of The Cigarette Papers. She has accepted honoraria ($50 to $1000 US
on a one-time basis) from the Canadian National Cancer Institute and AHRQ for
grant review, Research Triangle Institute and Health Systems Research, Inc. for
methodological consultation, the Friends Research Institute for a talk on
financial conflicts of interest and clinical trials, The Association of Medical
Writers and Dartmouth University for talks on reporting of scientific research
in the lay press, and the World Health Organization and Pomona University -
European Union Center for talks on public commentary on the Framework
Convention on Tobacco Control, Kaiser Permanente for talks on a) evaluating the
quality of research and b) tobacco industry manipulation of research, and the
World Conference on Clinical Pharmacology and Therapeutics for a talk on
managing financial conflicts of interest in clinical trials. She has received consulting fees (four
times) from the University of Colorado for conducting workshops in
evidence-based medicine.
KATHIE
CLARK, Centre Representative,
Cochrane Collaboration Steering Group until 3 October 2004, then Co-Chair of
the Cochrane Collaboration Steering Group; Co-Convenor, Monitoring and
Registration Group, until 3 October 2004, then Convenor of the Publishing
Policy Group; Member, Colloquium Policy Advisory Group; Member, Consumer
Network.
Kathie
Clark is Co-Director of The Canadian Cochrane Network and Centre (CCN/C). She
is employed full-time by the CCN/C that is currently funded by the Canadian
Institutes of Health Research, and received donations in 2004 from the Canadian
Chiropractic Protective Association.
MIKE
CLARKE, Co-Chair, Cochrane
Collaboration Steering Group, Convenor of the Publishing Policy Group and
Treasurer (until 3 October 2004); Director, UK Cochrane Centre;
Co-Co-ordinating Editor, Cochrane Methodology Review Group; Editor, Breast
Cancer Collaborative Review Group; Co-Convenor, Cochrane Individual Patient
Data Meta-Analyses Methods Group:
Mike
Clarke is employed by the Milton Keynes Primary Care Trust on behalf of the
Department of Health in England, as Director of the UK Cochrane Centre for four
days per week. This is a fixed term contract, the renewal of which is dependent
upon the value placed upon his work, that of the UK Cochrane Centre, and of The
Cochrane Collaboration more widely by the Department of Health. He is also
employed by Cancer Research UK to work one day per week at the Clinical Trial
Service Unit, University of Oxford, UK, primarily on systematic reviews of
treatments for early breast cancer. He prepares a regular contribution for the
National electronic Library for Health in the UK, for which he receives
payment. He is also paid for teaching on the University of Oxford's MSc in
Evidence Based Health Care course and for supervising postgraduate students. He
is not paid to act in any of his roles that relate to the central organisation
of The Cochrane Collaboration. He has not knowingly received any personal
funding direct from manufacturers of health care products, and cannot recall
accepting any hospitality from such companies, but he will correct any errors
in regard to this as soon as they are brought to his attention. He has received
payment for speaking and for writing from some journals and organisations,
including the American Society of Clinical Oncology. He referees for several
Cochrane Collaborative Review Groups, journals and funding agencies, and has
received little or no financial remuneration for any of this work. Neither he,
nor his immediate family, holds any shares or stocks in any company. Members of
his family have experienced specific health problems that influence some of the
choices he makes with regard to the work that he does. He does not believe that
any religious, political or other beliefs he may hold have a strong biasing
influence on any of his work, apart from his desire to help people achieve
better health through well-informed decision-making.
MARK
DAVIES, Collaborative Review Group
Representative (of Cochrane Authors/Reviewers), Cochrane Collaboration Steering
Group; Funding Arbiter (fundingarbiter@cochrane.org); Member, Cochrane
Collaboration Publishing Policy Group; Member, Cochrane Collaboration Quality
Advisory Group; Author/Reviewer, Anaesthesia, Neonatal and Skin Collaborative
Review Groups; Peer Reviewer, Anaesthesia Collaborative Review Group:
Mark
Davies is a consultant neonatologist: part of his income is derived from
private practice in neonatology. He has acted as a consultant to BMJ Books
reviewing manuscripts and proposals; but no other for-profit companies. As far
as he is aware he has no shares in any company with health care interests. He
recently co-edited and published 'Pocket notes on neonatology' (ISBN
0-9750756-0-8) where the printing costs were partially met by grants from
Fisher & Paykel Healthcare Pty Ltd and Abbott Australasia Pty Ltd. He is
not aware of any other potential conflicts of interest.
JON
DEEKS, Methods Group Representative,
Cochrane Collaboration Steering Group; Treasurer (from 3 October 2004);
Co-Convenor, Statistical Methods Group:
Jon
Deeks was funded one day per week from April 2004 to September 2004 by The
Cochrane Collaboration, and will be funded one day per fortnight from October
2004 to September 2005, to progress the Cochrane Diagnostic Reviews Initiative.
He receives payment from the British Medical Journal for statistical reviewing
and attending editorial meetings. Jon currently has no industry links, but has
occasionally worked as a paid methodological consultant to industry.
ZBIGNIEW
FEDOROWICZ, Collaborative Review
Group representative (of all members of Collaborative Review Groups), Cochrane
Collaboration Steering Group (from 3 October 2004); Member, Health Related
Quality of Life Methods Group, Member and Peer Referee, Oral Health Group;
Member, Eyes and Vision Group, and Health Promotion and Public Health Field:
Zbigniew
(Zbys) Fedorowicz is currently employed as a civilian clinician at the United
States Naval Dental Center, Europe, Branch Dental Clinic in Bahrain. This is
currently his sole source of income and he has no conflicts of interest to
declare.
DAVINA
GHERSI, Collaborative Review Group Representative
(of Review Group Co-ordinators and Trials Search Co-ordinators), Cochrane
Collaboration Steering Group; Editor and Review Group Co-ordinator, Cochrane
Breast Cancer Collaborative Review Group; Member, Cochrane Cancer Network;
Member, Cochrane CENTRAL Advisory Group; Member, Steering Group Executive;
Author/Reviewer, Ear, Nose and Throat Disorders Collaborative Review Group;
Advisory Board Member, Methodology Collaborative Review Group; Convenor,
Prospective Meta-Analysis Methods Group:
Davina
Ghersi is the Review Group Co-ordinator and an Editor of the Cochrane Breast
Cancer Group, and Co-Convenor of the Prospective Meta-Analysis Methods Group,
neither of which receive funds from for-profit organisations. She does not act
as a consultant to any for-profit organisation and has no shares in any company
with health care interests.
SALLY
GREEN, Centre Representative,
Cochrane Collaboration Steering Group; Director, Australasian Cochrane Centre;
Author/Reviewer, Musculoskeletal Collaborative Review Group; Co-Convenor,
Quality Advisory Group, Handbook Advisory Group, and Monitoring and
Registration Group:
Sally
Green is employed by Monash University as Director of the Australian Cochrane
Centre for four days per week. The Centre is fully funded by a grant from the
Australian Commonwealth Department of Health and Ageing. One day a week she
conducts private physiotherapy practice in a practice of which she is the sole
owner. She has no shares in any other company with health care interests. Sally
Green holds research grants from the Australian Research Council, the National
Health and Medical Research Council of Australia, the Commonwealth Department
of Health and Ageing, the Australian National Institute of Clinical Studies,
and the Wellcome Trust, all not-for-profit organisations. She is paid a nominal fee for supervising
postgraduate students, marking academic work, and contributing to journals. She
has not knowingly received any personal funding direct from manufacturers of
health care products, but has been co-investigator of a clinical trial in which
one intervention was supplied free of charge by Sigma Pharmaceuticals.
DAVID
HENDERSON-SMART, Collaborative Review
Group Representative (of all members of Collaborative Review Groups) (until 3
October 2004); Publication Arbiter (dhs@perinatal.usyd.edu.au); Member of the
steering group of the Australasian Cochrane Centre; Chair of the Renal Review
Group Advisory Board; Member and Australasian Co-ordinator of the Neonatal
Collaborative Review Group; Member of Pregnancy and Childbirth Collaborative
Review Group; Member of the Effective Practice and Organization of Care
Collaborative Review Group:
David
Henderson-Smart is Director of the Centre for Perinatal Health Services
Research at the University of Sydney. His salary is provided by New South Wales
Health through the Central Sydney Area Health Service, where he is a member of
the Department of Neonatology, Royal Prince Alfred Hospital. He is an advisor
to the NSW Health and the National Health and Medical Research Council of
Australia. He is a member of the executive of the Australian and New Zealand
Neonatal Network, which receives funding from Abbott Australia to run its
database. He does not currently act as a consultant to any for-profit organisation
and has no shares in any company.
STEFF
LEWIS, Collaborative Review Group
Representative (of all members of Collaborative Review Groups), Cochrane
Collaboration Steering Group; Editor, Stroke Collaborative Review Group; Member
(and, from 3 October 2004, Co-Convenor), Monitoring and Registration Group;
Co-Convenor, Statistical Methods Group; Member, Cochrane CENTRAL Management
Advisory Group:
Steff
Lewis is a statistician based in a clinical trials unit in Scotland, UK. As part of this role, she is the trial
statistician for a clinical trial funded by PPP, but with some active drug and
placebo supplied by Boehringer Ingelheim free of charge. She is also the trial statistician for a
trial funded by Chest Heart and Stroke Scotland and the Medical Research
Council, but with medical devices provided free of charge by
Tycohealthcare. Steff is paid by the
Cochrane Stroke Group for one day per week as statistical editor. She does not currently act as a consultant
to any for-profit organisation and has no shares in any company.
JIM
NEILSON, Co-Chair, Cochrane
Collaboration Steering Group; Co-ordinating Editor, Pregnancy and Childbirth
Collaborative Review Group; Peer Reviewer, Cystic Fibrosis and Genetic
Disorders Collaborative Review Group; Convenor, Steering Group Executive;
Member, Publishing Policy Group; Member, Handbook Advisory Group:
Jim
Neilson is co-principal investigator of a clinical trial in Malawi, funded by
the Wellcome Trust, but with active drug and placebo supplied by Pfizer free of
charge. He does not act as a consultant to any for-profit organisation and has
no shares in any company with health care interests. He does no private clinical practice but does act as a
remunerated expert in some legal cases, usually involving claims about obstetric
origins of cerebral palsy.
JORDI
PARDO PARDO, Centre Staff
Representative, Cochrane Collaboration Steering Group; Administrator,
Iberoamerican Cochrane Centre; Member, Colloquium Policy Advisory Group;
Member, Publishing Policy Group:
Jordi Pardo is the Administrator of the Iberoamerican Cochrane Centre. He is employed full-time by the Fundación de Gestió Sanitària de l'Hospital de la Santa Creu i Sant Pau, a private not-for-profit charity. The Centre receives support from several sources, including pharmaceutical companies, as listed in the Centre's module in The Cochrane Library and on the Centre's website (www.cochrane.es). Jordi does not believe that any religious, political or other beliefs he holds have a strong biasing influence on any of his work. Neither he, nor his immediate family, holds any shares or stock in any company. Jordi is not aware of any other potential conflicts of interest.
ROB
SCHOLTEN, Centre Representative,
Cochrane Collaboration Steering Group, (from 3 October 2004); Member, Quality
Advisory Group, Statistical Methods Group, and Screening and Diagnostic Tests
Methods Group; Author/Reviewer, Back, Dementia and Cognitive Improvement,
Depression Anxiety and Neurosis, Heart, and Neuromuscular Disease Collaborative
Review Groups; Chair, Thomas C. Chalmers Award Committee, 2004:
Rob
Scholten is Co-Director of The Dutch Cochrane Centre, which is currently funded
by the Dutch Ministry of Health. He is employed full-time by the Academic
Medical Center of the University of Amsterdam. Rob is not aware of any
potential conflicts of interest.
SILVANA
SIMI, Consumer Network
Representative, Cochrane Collaboration Steering Group and Member, Steering
Group Executive (until 3 October 2004); Editor, Multiple Sclerosis
Collaborative Review Group; Consumer Representative, Multiple Sclerosis
Collaborative Review Group; Member, Cochrane Consumer Network Governing
Council:
Silvana
Simi has a stable position as a senior researcher at the Italian National
Research Council. As far as she can remember, she has never received funding
directly from manufacturers of health care products in her research career. She
recently received payment and hospitality for giving a seminar from
GenPharmTox, a biotechnology company, established by a former colleague at
Munchen University. She does not act as a consultant to any for-profit
organization, and has no shares in any company with health care interests. One of her current research projects is to
study the mechanisms of in vitro genotoxicity of complex mixtures such as
cigarette smoke condensate: this project has been financed by the Italian
Ministry of Agriculture. A member of
her family is suffering from a severe disease which can influence choices in
the work she does.
PETER
TUGWELL, Collaborative Review Group
Representative (of Co-ordinating Editors), Cochrane Collaboration Steering
Group; Co-ordinating Editor, Musculoskeletal Collaborative Review Group:
Peter
Tugwell has received travel and research support from dozens of pharmaceutical
firms (PFs) for over thirty years. This support has permitted research
associates to work on methodologic projects of no commercial interest, has
supported students and fellows who otherwise would not have been able to get an
education, and has provided partial support for the planning and organization
of scientific meetings in which the funder had no say about subject matter,
content, or speakers. He has never received personal salary research support or
awards from PFs. He was principal investigator for randomized trials of
cyclosporine published in the Lancet and NEJM; these were funded in part but
never in whole by PFs who had no access to the emerging data, no control over
whether or when the studies stopped, and no veto power over any publications or
presentations. The Musculoskeletal Collaborative Review Group has received
unrestricted grants for staff support in carrying out systematic reviews, a
number of which failed to draw favorable conclusions about donor's drugs. While
Chair of Medicine at the University of Ottawa, Peter prohibited PFs from solo
support of department educational rounds or from any say in content. He also
enforced a policy of using generic names. When he served on the US Government
National Science Panel examining the relationship between silicone breast
implants and connective tissue disorders, he was certified by a U.S. District
Court Judge to be free of any industry influence.
JANET
WALE, Consumer Network
Representative, Cochrane Collaboration Steering Group; a freelance editor and
consumer representative on Commonwealth of Australia and Western Australian
health committees; a consumer for the Cochrane Acute Respiratory Infections,
Anaesthesia, Musculoskeletal, Musculoskeletal Injuries, and Heart Collaborative
Review Groups, and a member of the Cochrane Consumer Network.
Janet
Wale has no conflicts of interest to declare.
ELIZABETH
WATERS, Field Representative,
Cochrane Collaboration Steering Group (from 3 October 2004); Director, Health
Promotion and Public Health Field; Member, Advisory Board of the Child Health
Field; Member, Non-Randomised Studies Methods Group; Member, Quality Advisory
Group; Member, Cochrane Heart, Pregnancy and Childbirth, Airways, and Effective
Practice and Organisation of Care Collaborative Review Groups:
Elizabeth
(Liz) Waters is employed by Deakin University as Chair in Public Health and is
a member of the Australian NHMRC Health Advisory Committee. She receives
funding from a range of research organisations to conduct research and
education programs of work. Neither she nor her family have shares in industry,
and she does not receive monies from industry or related organisations. She
very occasionally receives monies for reviewing research grants from
international universities. Liz is not aware of any potential conflicts of
interest.
Declaration of interests of Director, Information Management System
MONICA KJELDSTRØM, Director, The Cochrane Collaboration Information
Management System; Director, Collaboration Trading Company; Member, Publishing
Policy Group; Member, Information Management System Group, Editorial Management
Advisory Group and RevMan Advisory Group; Member, Quality Advisory Group;
Author/Reviewer, Peripheral Vascular Diseases Group:
Monica Kjeldstrøm is
employed by the Rigshospitalet, Copenhagen, Denmark, as Director of the
Cochrane Collaboration Information Management System. Her employment is
permanent but her position can be changed by the Rigshospitalet. The
Rigshospitalet provides her only source of income. Monica Kjeldstrøm was given,
and continues to hold, shares in a small Danish biotechnology company, but is
unable to trade in these and does not derive any income from them. She will not
influence the conduct of any review in which this company might have a
financial interest.
Declaration of interests of Secretariat staff:
NICK
ROYLE, Chief Executive Officer, The
Cochrane Collaboration; Member, Campbell and Cochrane Economic Methods Group;
Member, Cochrane Screening and Diagnostic Tests Methods Group: As part of his
role as Chief Executive Officer, Nick Royle has a responsibility for developing
strategic alliances and for developing new and maintaining existing funding for
The Cochrane Collaboration. As such he is precluded from participating in the
process of developing the Collaboration’s policy on conflicts of interest, but
will take a major role in its implementation. He does not currently act as a
consultant to any organisation, although he has formerly been a member of
government committees on drug and alcohol misuse, and advised organisations
involved in helping those with drug and alcohol misuse problems. With the
exception of a small number of shares in a household and general insurance
company obtained as a result of a privatisation, he holds no direct shares in
any company, but has investments in general funds such as pension funds and no
knowledge of which companies these invest in.
JINI
HETHERINGTON, Administrator and
Company Secretary, Cochrane Collaboration Secretariat: Jini Hetherington holds
no stocks or shares, and is not aware of any potential conflicts of interest.
CLAIRE
ALLEN, Deputy Administrator, Cochrane
Collaboration Secretariat; Consumer (commenting on protocols and reviews) with
the Ear, Nose & Throat, Peripheral Vascular Diseases, Airways, and Acute
Respiratory Infections Collaborative Review Groups; Member of the Complementary
Medicine Field Advisory Board; Author/Reviewer in the Menstrual Disorders and
Subfertility Group; Consumer on a randomised controlled trial of acupuncture
for migraine funded by the NHS; Consumer on the NHS Priorities Project for
Complementary Therapies for Cancer funded by the NHS; Commentator on 'Hot
Topics' for Informed Health Online.
Claire Allen is not aware of any potential conflicts of interest.
LOUISE
KITCHENER, Administrative Assistant,
Cochrane Collaboration Secretariat:
Louise Kitchener holds no stocks or shares, and is not aware of any
potential conflicts of interest.