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Board Meeting Minutes
American Academy of Emergency Medicine
Minutes of Board of Directors Conference Call
June 25, 2002
IN ATTENDANCE: Joseph Wood, MD, JD; Robert McNamara, MD; A. Antoine Kazzi, MD;
Tom Scaletta, MD; Carol Barsky, MD; Howard Blumstein, MD; William Durkin, Jr.,
MD; James Li, MD; Raymond Roberge, MD; Kevin Rodgers, MD, Paul Sierzenski, MD;
Scott Weiner, MD. Absent: Anthony DeMond, MD; Geoffrey Mitchell, MD. Staff: Kay
Whalen.
Approval of May 18-19, 2002 Board of Directors Meeting Minutes
Dr. Wood welcomed everyone to the call and turned the Board's attention to the
first agenda item. After a review of the minutes from the St. Louis Board
meeting, Dr. Scaletta moved and Dr. Durkin seconded that the May 18-19, 2002
minutes be approved. MOTION PASSED UNANIMOUSLY.
President's Report
Dr. Wood reported he and Dr. Kazzi had met with the ACEP leadership in St. Louis
during the SAEM meeting. At that time, AAEM had asked ACEP if there were ways in
which the two organizations would be able to work together legislatively. Dr.
Carius, ACEP president, contacted Dr. Wood to decline AAEM's offer to work
together. The Committee that was established during the strategic planning
session and chaired by Dr. McNamara will now identify various options for
legislative representation.
Dr. McNamara and Dr. Kazzi will both be speaking at residency programs in July.
Treasurer's Report
Dr. Scaletta then reviewed the May 31, 2002 financial statements which were
included in the agenda packet. He noted that, after the $55/member dues
assignment for each AAEM member, the Scientific Assembly would, at a minimum, be
a break-even proposition. Dr. McNamara questioned the significant increase in
catering costs. Ms. Whalen responded that in addition to the higher cost of
catering, a second lunch in the exhibit hall had been added. The Board did not
feel that this would be necessary for 2003.
Dr. Scaletta also noted that he had asked staff to investigate a higher interest
rate on AAEM's investments. Staff researched the option that Dr. Li had
suggested, but this investment is only available to individuals. Interest rates
on longer term CDs are paying slightly higher interest rates than AAEM's money
market account, but purchasing a CD would lock us into a relatively low interest
rate at the current time.
Membership
Ms. Whalen presented the membership report. Full voting members are currently
5.9% ahead of last year's pace. Associate members are 60% of last year's pace.
In fact, membership in all categories has increased.
The Board then turned its attention to Dr. Kazzi's nomination of Dr. Hashim
Allam, the Undersecretary of Health for Emergency Medical Services in Egypt, for
honorary international membership. Dr. Roberge noted that AAEM's bylaws limit
membership in this category to presidents of international medical societies.
Dr. Kazzi stated that Dr. Allam may establish an Egyptian Emergency Medicine
Society. Dr. Roberge moved and Dr. Scaletta seconded that the nomination of
Dr. Hashim Allam as an international member be tabled. MOTION PASSED
UNANIMOUSLY.
Conference Call Scheduling
Dr. Wood then noted that he had received requests to schedule Board meetings and
conference calls for the remainder of the year. After discussion, the remaining
full Board conference calls were scheduled for August 12th and December 9th. The
Board will also meet in-person in Chicago on October 26th.
Certification Cards
Dr. Scaletta then presented a draft of cards that state Emergency Medicine
physicians are qualified in cardiac, pediatric and trauma resuscitation due to
the training and skills necessary to become board certified. Dr. McNamara moved
and Dr. Scaletta seconded that AAEM provide cards to its fellows as a
membership benefit. After much discussion, Dr. Roberge moved and Dr.
Scaletta seconded that the previous motion regarding resuscitation cards be
tabled. MOTION PASSED 6-5. Dr. Scaletta then moved and Dr. McNamara seconded
that AAEM send an e-mail to a sample of AAEM fellows to determine if AAEM's
membership would find resuscitation cards helpful. MOTION PASSED
UNANIMOUSLY. If the membership would find these cards valuable, Ms. Whalen will
seek legal counsel regarding any possible trademark issues.
Draft Code of Ethics
Dr. Wood then drew the Board's attention to the draft code of ethics that was
included in the agenda packet. He noted that the Executive Committee had
reviewed this document and recommended adoption. Dr. Scaletta moved and Dr.
Kazzi seconded that AAEM adopt the code of ethics as presented. MOTION
PASSED 10-1.
Amiodarone Position Statement
Dr. Li then asked the Board to consider modifying or removing AAEM's position
statement on amiodarone based on new evidence. Dr. Li moved and Dr. McNamara
seconded that the amiodarone work group reconsider the position statement
based on new evidence unless the efforts of the work group have already
addressed this issue. MOTION PASSED UNANIMOUSLY.
Mediterranean Congress Budget 2003
Dr. Kazzi then reported that the dates of the 2003 Mediterranean Congress in
Spain have been moved to September 20-23. The budget included in the agenda book
was still preliminary. AAEM staff will be more involved in the planning of the
2003 meeting to ensure ACCME requirements and other financial reporting
requirements will be met.
Guidelines for Medical Research
Dr. Li then outlined his reasons for developing guidelines for researchers
involved in clinical trials. Dr. Li moved and Dr. McNamara seconded that the
following be approved:
Guidelines for Researchers Involved in Manufacturer-sponsored Trials
Background
As medical research of drugs and devices has evolved, the quality of available
evidence has benefited from increasing numbers of well designed randomized
controlled trials, leading directly to reductions in selection bias. An
additional source of potential bias is found when manufacturers with interests
vested in positive trial outcomes sponsor trials themselves. In order
to reduce this type of bias, the following guidelines are presented for
medical journals that publish manufacturer-sponsored research. These guidelines
are meant to supplement authorship disclosure of potential conflicts.
Recommended supplement to authorship guidelines
Manufacturers sponsoring trials should make significant efforts to remove
individual investigators
from potential funding bias. To this end, study protocols should be initiated
by investigators who are neither compensated nor employed by the manufacturer.
Such trials should be executed and their results analyzed without any
contribution from the study sponsors. Additionally, trial reports should
be written entirely by the study authors and not be sent to agents of
the sponsoring manufacturer for prepublication review.
Authors who submit manuscripts according to these guidelines are encouraged
to include the
following language in their Methods:
"The manufacturer, XXX, donated medications and funding for the trial,
but agreed that the trial be conducted independently in order to reduce
funding bias. This agreement specified that results of the trial could
be published in the particular case where an outcome could negatively
impact the
manufacturer's market value. Accordingly, the trial was designed, conducted,
analyzed, interpreted, and written by investigators independent of XXX,
and was not sent to agents of XXX for prepublication review or approval."
For review articles, authors should explicitly state that they are directly
responsible for writing.
Substitute authoring (also known as "ghost writing") should be clearly
identified.
Recommendations to editors
Manuscripts from manufacturer-sponsored trials where efforts have been
made to eliminate funding bias should be given priority for publication
over similar manuscripts where funding bias remains possible.
Employees of sponsors must be clearly identified if involved in manuscript
authorship. Any other
relationships between authors and sponsors must also be clearly identified
within the author section
of the publication.
Recommended supplement to expert guideline classification
In addition to classifying research evidence by trial design (where, for
example, a randomized
controlled trial is considered Level I evidence), expert guidelines should
also denote potential funding bias. The highest level of evidence should
be reserved for randomized controlled trials that are clearly independent
of such bias.
MOTION PASSED UNANIMOUSLY.
Public Service Announcement
Dr. Li then reported that he had researched the possibility of producing
a public service announcement (PSA) stressing the importance of board
certification in Emergency Medicine. He estimated the costs to be about
$5,000. After discussion, Ms. Whalen volunteered to research the costs
of production and distribution of such a PSA further.
New Business
Dr. Wood announced that AAEM had been accepted into the Specialty and
Service Society (SSS) of the AMA. He also noted that AAEM has received
a number of positive e-mails in response to our letter to Child magazine.
We also had 10 hospitals apply to be listed on the
www.911emergency.org website.
There being no further business, the conference call meeting was adjourned.
Respectfully submitted,
Kay Whalen
Organizational Director
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