Validity of the convergence insufficiency symptom survey: a confirmatory study.
Validity of the convergence insufficiency symptom survey: a confirmatory study.
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DOI:
10.1097/opx.0b013e3181989252
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发表时间:
2009-04
期刊:
影响因子:
--
通讯作者:
Convergence Insufficiency Treatment Trial (CITT) Investigator Group
中科院分区:
文献类型:
--
作者:
Rouse M;Borsting E;Mitchell GL;Cotter SA;Kulp M;Scheiman M;Barnhardt C;Bade A;Yamada T;Convergence Insufficiency Treatment Trial (CITT) Investigator Group
The objectives of the present study were to evaluate whether investigator bias influenced the Convergence Insufficiency Symptom Survey (CISS) scores of children with normal binocular vision (NBV) in our original validation study, reevaluate the usefulness of the cut-off score of 16, and reexamine the validity of the CISS. Six clinical sites participating in the Convergence Insufficiency Treatment Trial (CITT) enrolled 46 children 9 - <18 years with NBV. Examiners masked to the child’s binocular vision status administered the CISS. The mean CISS score was compared to that from the children with NBV in the original, unmasked CISS study and also to that of the 221 symptomatic CI children enrolled in the CITT. The mean (±SD) CISS score for 46 subjects with NBV was 10.4 (±8.1). This was comparable to that from our prior unmasked NBV study (mean = 8.1(± 6.2); p = 0.11), but was significantly different from that of the CITT CI group (mean = 29.8 ± 9.0; p < 0.001). Eighty-three percent of these NBV subjects scored less than 16 on the CISS, which is not statistically different from the 87.5% found in the original unmasked study (p = 0.49). Examiner bias did not affect the CISS scores for subjects with NBV in our prior study. The CISS continues to be a valid instrument for quantifying symptoms in 9 to <18 year-old children and these results confirm the validity of a cut-point of ≥ 16 in distinguishing children with symptomatic CI from those with NBV.