ASM Quality Workshop
Today we participated in the
Quality Workshop at the Annual General Meeting (ASM) for the American Society
for Microbiology. In some respects this
is the perfect union. The ASM attracts
about a bazillion people from around the world.
It is big enough to fill almost every hotel in Denver. The Quality Workshop is a bit of a niche
interest, but we managed to have people from across the US, Canada Lebanon,
South Africa, Australia and the Republic of Cameroon. Small conferences
will attract interested folks, and mega-meetings will attract broad
international crowds. We were lucky to
end up with the best of both.
Without wanting to overstate the situation, I think the light has gone
on in the United States. While at one time the CLIA regulations were
the vanguard leaders in the world, many would say at 25 years old, CLIA has
become a tired millstone in serious need of revision. While there are many US laboratories that don’t
give a damn to quality, those that are recognize that being accredited to CLIA
provides no evidence of interest in making their laboratory better.
Fast, cheap, east, mandatory and sufficient; good-enough is good-enough.
The folks that attended the workshop were of a different mindset; interested
in learning about international quality, with higher aspirations for their
laboratory’s reputation and recognition.
The meeting was put together by CDC and included two CDC speakers, a
well-informed speaker from another laboratory and me. One can find the names of the other speakers
by going to the ASM Annual General Meeting site and looking for speakers at workshop
WS:04.
It was an excellent meeting full of practical tips, and perspective.
I gave a good overview of why Quality Management belongs in every
laboratory.
A very good presentation was
given on CLSI and that organization’s participation in the Quality area. A very good crosswalk was presented on how
CLSI guidelines lined up with the requirements of ISO standards. It was pretty clear that CLSI is contributing
to US medical laboratories by providing a series of documents that help
implement Quality.
What was really interesting to me was the presentation on measurement
uncertainty from a laboratory in the US that had decided to get accredited to
ISO/IEC 17025 very early on, had has had to struggle with MU. A model for application of MU for
quantitation of urine cultures was presented.
I thought it truly excellent. We
all agreed that MU is an irrelevant waste of time, but has to be dealt with if
a laboratory wants to benefit from the achievement of ISO accreditation. Having to jump through hoops purely to
satisfy accreditation bodies may be stupid and evil, but it unfortunately an
unavoidable stupid evil. What Alice presented
was a model that would get it done in as painless a manner possible. And that probably is the best way
forward.
And more to the point, the information is generated solely for
internal holding. Do not present the information to anyone, other
than the accrediting body.
What I thought amusing was her mentioning that the accrediting body
required her to actually to through the arithmetic during their site
visit. Just sad.
The last presentation was unfortunately cut short because so many
questions were being asked. It was too
bad because it was shaping up as an excellent presentation fo some practical tips
on implementing Quality on an voluntary level.
As mentioned, it your laboratory is not going to go for full ISO
accreditation, you are still better off implementing some easy steps along the
way, and gradually building your Quality inventory. It is not the best way to implement Quality
but if management and staff are committed, it can work. I am thinking of inviting her to give the presentation
again in Vancouver at the POLQM Medical Laboratory Quality Conference Meeting
October 16-17-18 2013.
If you want to meeting an impressive faculty, plan to come to the
meeting. If you want to learn and
discuss and debate Quality with peers, plan to come to the meeting. It you want to participate in a World
Standards Day celebration, plan to come to the meeting.
More info VERY SOON.
M
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