This collection
is approved under the following terms of clearance: Upon publishing
a new 60-day and 30-day Federal Register Notice, CMS will provide
the public and OMB with a supplemental document that crosswalks all
changes (technical and substantive) made to the revised ICR. The
document should include an explanation of each change from the
previous approval, the reason why the change is necessary and the
citation or reference to the statute, regulation or guidance
document that support the need for the change. The crosswalk should
also address an increase or decrease in burden for each
change.
Inventory as of this Action
Requested
Previously Approved
09/30/2010
36 Months From Approved
09/30/2007
11,986,053
0
11,087,565
9,050,817
0
9,339,184
0
0
0
This collection requires HHAs to use a
standard core assessment data set, the OASIS, to collect
information and to evaluate adult non-maternity patients. In
addition, data from the OASIS will be used for purposes of case mix
adjusting patients under home health PPS and will facilitate the
production of necessary case mix information at relevant time
points in the patient's home health stay. Modifications were
previously made to the OASIS forms to allow for the preservation of
masking of personally identifiable information for the
non-Medicare/non-Medicaid individuals.
US Code:
42
USC 1395x Name of Law: Home Health Agency
The burden associated with
these proposed changes includes possible training of staff, the
time and effort associated with downloading a new form and
replacing previously pre-printed versions of the OASIS, and
utilizing updated vendor software. However, CMS will be removing or
modifying existing questions in the OASIS data set to accommodate
the requirements referenced above. In addition, as a result of the
proposed changes of CMS-1541-P, we expect that the claims
processing system is expected to automatically adjust the therapy
visits, upward and downward on the final claim, according to the
information on the final claim. Consequently, the HHA will no
longer have to withdraw and resubmit a revised claim when the
number of therapy visits delivered to the patient is higher than
the level report on the RAP. Therefore, CMS believes the burden
increase associated with these changes is negated by the removal or
modification of several current data items. The overall burden to
OASIS was decreased by 28% in the OASIS data set. The burden has
increased since the last submission due to an increase in the
number of respondents.
$0
No
No
Uncollected
Uncollected
Uncollected
Uncollected
Saleda Perryman
No
On behalf of this Federal agency, I certify that
the collection of information encompassed by this request complies
with 5 CFR 1320.9 and the related provisions of 5 CFR
1320.8(b)(3).
The following is a summary of the topics, regarding
the proposed collection of information, that the certification
covers:
(i) Why the information is being collected;
(ii) Use of information;
(iii) Burden estimate;
(iv) Nature of response (voluntary, required for a
benefit, or mandatory);
(v) Nature and extent of confidentiality; and
(vi) Need to display currently valid OMB control
number;
If you are unable to certify compliance with any of
these provisions, identify the item by leaving the box unchecked
and explain the reason in the Supporting Statement.