Approved for use
through 9/93 under the condition that the next submission for OMB
review contains an updated analysis of beneficiary non response.
This analysis should evaluate non response on an item by item
basis, as well as the general non response rate for the entire core
instrument and each supplement. OMB continues to have reservatio as
to whether the response rates of this instrument are sustainable
over time, thereby ensuring that the data continues to be useful
for longitudinal analysis.
Inventory as of this Action
Requested
Previously Approved
09/30/1993
09/30/1993
02/28/1992
40,000
0
14,000
40,000
0
14,000
0
0
0
ROUNDS 2-10 COLLECT COST AND
UTILIZATION DATA FOR THE HOUSEHOLD AND NURSING HOME POPULATION.
INFORMATION COLLECTION INCLUDES: INPATIENT HOSPITALIZATION,
EMERGENCY ROOM, OUTPATIENT CLINICS, PROVIDER USE, PRESCRIPTION
MEDICATION AND OTHER MEDICAL EQUIPMENT. COST, CHARGES AN SOURCES OF
PAYMENT WILL BE COLLECTED FOR EACH UTILIZATION.
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.