Critique Letter: Purpose And Use
from
the Fall 1999 issue
When
laboratories successfully achieve accreditation, they will receive
two letters from the ICAVL. The first letter arrives within
weeks of the decision, announcing that accreditation has been
granted and commending the staff for their commitment to providing
quality care. Enclosed with the letter is an Accreditation
Portfolio containing a camera-ready logo, press release,
media list and the certificates of accreditation. A second letter,
the critique letter, is sent a few months after the original
notification letter. Composed of comments made by the ICAVL's
application reviewers, the critique letter provides guidelines
and recommendations for achieving reaccreditation and, more
importantly, for achieving the goal of providing top-quality
diagnostic evaluations.
"The
critique letter serves as a formal record of the quality of
service provided by a laboratory at the time of accreditation
and is one of the most important benefits of ICAVL accreditation,"
explains the previous Technical Manager Gail Sandager, RN, RVT.
"Sometimes laboratory staff members think that the ICAVL
is telling them what they do wrong, but successfully acquiring
accreditation recognizes that they do the most important things
right."
The
critique letter is designed to serve as a tool to address issues
raised during the review process. By providing the findings
and comments of the application reviewers and Board Of Directors,
the ICAVL anticipates that accredited laboratories will continue
to explore methods of improving the quality of care provided.
"Really, we would be short-changing the laboratory and
the public if we just awarded accreditation and provided no
feedback. Our responsibility to laboratories is that we pay
attention to detail and provide a high-quality review of the
application," Sandager said. "It also provides us
with a means to assess the growth of the laboratory at the time
of reaccreditation." When laboratories apply for reaccreditation
in three years, staff members must demonstrate that they have
addressed the issues raised in the critique letter.
HOW
THE CRITIQUE LETTER IS CREATED
The
creation of the critique letter begins with the application
reviewers. Each application is reviewed by two reviewers who
work independently of one another. Along with each application,
reviewers receive an abbreviated version of the Essentials
and Standards which focuses on particular sections within
the application. As the reviewers assess each laboratory's application,
they use the abbreviated version to note deficiencies and to
make positive comments. They return the reviewed application
and their recommendations to the ICAVL where the Technical Manager
collates the data from both reviewers. Any discrepancies between
the comments are individually investigated by pulling the original
application and reviewing the specific item. Sometimes, discrepancies
between reviewer comments are the result of missing documents
between the original application and the photocopy, both provided
by the laboratory. Therefore, it is recommended that a laboratory
staff member carefully verify that all items were photocopied
and included in both copies before submitting the application
to the ICAVL.
The
Technical Manager also checks the reviewers' recommendations
to substantiate relevance to the Essentials and Standards.
Some issues will need to be addressed immediately in order for
the laboratory to achieve accreditation. These issues often
result in decisions to delay or site visit a laboratory. Other
issues can be corrected at a later time, and it is these comments
that laboratories receive in the critique letter after a final
decision is made. The collected information is then used to
construct the critique letters for accredited laboratories.
CONTENT
OF THE CRITIQUE LETTER
There
are three important things that laboratory staff should know
when reading their own critique letter.
1.
Critique letters contain comments that provide a general
overview of the application and do not necessarily address
specific cases. The critique letter is designed to deal
with issues regarding the medical and technical staff and
the conduct and performance of examinations; however, the
letter often addresses general findings rather than specific
occurrences in the application. For example, a laboratory
may receive a number of comments relating to documentation
issues. While the laboratory may perform quality examinations,
they did not submit enough documentation to demonstrate the
level of quality required by the Essentials and Standards.
In Figure
1: Sample Critique Letter on page seven of the Newsletter,
items one and two are examples of comments providing a general
overview of the ICAVL's observations.
2.
Critique letters contain recommendations for providing
improved diagnostic testing. Recommendations often include
specific suggestions for laboratory improvement not currently
required in the Essentials and Standards, recognizing
that many laboratories may not have the resources or capability
to make changes immediately. The ICAVL anticipates that laboratory
staff will discuss the critique letter recommendations during
laboratory meetings and make earnest efforts to implement
positive change. The third item in the sample critique letter
is an example of a recommendation by the ICAVL.
3.
Critique letters contain requirements that must be documented
to achieve reaccreditation. Because accreditation is an
inclusive process, the ICAVL occasionally grants accreditation
based on somewhat limited documentation with the expectation
that those procedures will be better documented in the application
for reaccreditation. Failure to address these issues will
result in reaccreditation being delayed. Item four in the
sample critique letter is an example of a comment relating
to a requirement for reaccreditation.
All
issues raised in the critique letter, whether recommendations
or requirements, must be addressed and documented by laboratory
staff before reaccreditation, particularly when comments concern
technical or reporting components of the examination. Technical
and reporting components are weighted most heavily during the
review process. Documentation of these issues should be demonstrated
in the minutes of staff meetings, in the protocols and quality
assurance procedures and in the case studies submitted with
the application.
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