Rek. Stein et al., Shortening the questionnaire for identifying children with chronic conditions: What is the consequence?, PEDIATRICS, 107(4), 2001, pp. NIL_111-NIL_115
Objective. To determine whether a reduced item set can identify children wh
o have chronic conditions with a level of at least 90% accuracy compared wi
th the complete Questionnaire for Identifying Children With Chronic Conditi
ons (QuICCC).
Background. The QuICCC was developed to operationalize a conceptually based
, noncategorical definition of chronic conditions developed by Stein et al.
It contains 39 item sequences administered to a parent that assess 3 types
of consequences: functional limitations; reliance on compensatory mechanis
ms or assistance; and service use or need above usual for age. The QuICCC h
as been validated and widely adopted as a means of identifying children wit
hout using a diagnosis checklist, but there is considerable interest in sho
rtening it.
Design/Methods. Through secondary analyses of 3 data sets (Ns = 1265, 1388,
and 4831), we identified a short list of items that identified >90% of chi
ldren who were identified by the 39-item QuICCC. We administered these 16 i
tems to 2 new samples of parents. In Study 1 we administered the 16 items i
n the shortened version first, followed by the other 23 items, and compared
the results on the short and reordered long versions. In Study 2, the 39-
and 16-item versions were each administered, one in person and the other by
phone, in random order to the same respondent within a 2-week period. Thes
e data were analyzed to compare the short and longer versions at the 2 time
points and within the single, longer 39-item format (simultaneous data).
Results. In Study 1 (N = 630) only 4 children were missed by the 16-item ve
rsion who were identified by the longer version (sensitivity 98.6%; specifi
city 100%; positive predictive value 100%; negative predictive value 98.8%
kappa 0.987). In Study 2 (N = 552), no children were missed by the 16-item
subset of the 39 items when looking at the simultaneous data. When the two
forms were administered 2 weeks apart, the 16-item version had a sensitivit
y of 87%, specificity of 90%, positive predictive value of 93%, negative pr
edictive value of 82%, and kappa of 0.78 compared with the longer QuICCC. T
hese results correspond exactly to the data obtained in a 2-week test-retes
t study for the QuICCC itself. The new form (the QuICCC-R) takes <2 minutes
to administer on average (range 1-4 minutes) compared with 7 to 8 minutes
for the full QuICCC.
Conclusions. The results met our criteria for agreement, and we conclude th
at the QuICCC-R is a satisfactory alternative for screening populations. Ho
wever, the full QuICCC has other applications beyond screening that may not
apply to the QuICCC-R, the shorter version.