Quality Indicators: Original CHSRA QIs
QI Versions: MDS+ versus MDS 2.0 and Variants
The quality indicators (QIs) originally were developed for use with CMS's
Multistate Nursing Home Case Mix and Quality Demonstration project. States
participating in the quality component of that demonstration (Kansas,
Maine, Mississippi, and South Dakota) used an expanded form of the Minimum
Data Set (MDS) known as the MDS+.
In order to allow use of the QIs beyond the demonstration, and in recognition
of CMS's planned move from the MDS+ to the MDS version 2.0, it was necessary
to define QIs using the MDS 2.0. It is not possible to directly apply
the QIs as defined for the MDS+ to the MDS 2.0.
The translation of the QIs for the MDS 2.0 faced two significant challenges.
First, there were some significant differences between the MDS+ and the
MDS 2.0. Some items were modified or redefined, others were deleted and
replaced with entirely new items. An example of an item that was modified
is the item related to the presence of contractures. The MDS+ defined
contractures (items H5b-f) as "restriction of full functional range of
motion of any joint due to any cause" (MDS+ Manual, page 6-53). The MDS
2.0 moved away from the concept of contractures to focus on range of motion.
Thus, the MDS 2.0 offers items G4a-f, as functional limitations in range
of motion. This item captures "the presence of (A) functional limitation
in range of joint motion or (B) loss of voluntary movement," and both
are defined as limitations that "[interfere] with daily functioning .
. . or [place] the resident at risk of injury" (MDS 2.0 Manual, page 3-95).
An example of an item that was replaced by an entirely new item is the
MDS+ item E1f, a checkbox indicating suicidal thoughts or actions. The
MDS 2.0 has no similar item. Items that changed or that did not exist
on the MDS 2.0 affected our ability to define QIs. While most QI definitions
are the same regardless of the assessment form used, some QI definitions
have been modified to reflect the differences in the data available from
the MDS 2.0.
The second major difference between the MDS+ and the MDS 2.0 was the
frequency and comprehensiveness of the data collected. In all cases, the
data was collected upon initial admission to the facility; at readmission
following temporary discharge to a hospital, other care facility, or home;
and on a quarterly basis. (A small number of assessments were conducted
for other reasons, in some states.) While the assessment schedule was
the same, within the demonstration states the full set of data were obtained
at each assessment. Currently states are using the MDS 2.0, however, there
are a variety of assessment options. The minimal requirement is that a
complete assessment be conducted upon admission, readmission, and annually;
quarterly assessments may collect only a subset of the information collected
at other times. Thus, the information needed to define a given QI may
be available when a complete assessment is completed, but not when the
data come from the partial quarterly assessment. Since the most frequent
reason for completing an MDS assessment is for a quarterly update, this
places a strong limitation on the calculation of the QIs.
There are other variations of the QIs depending upon the types of quarterly
assessments used (e.g., RUGS III or a full assessment) or if supplemental
case mix information (Section T of the MDS is collected or Section U,
medication information is used). For copies of other matrices defined
by these other assessments or supplemental information please contact
Lorraine Roberts.
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