Elsevier

Ophthalmology

Volume 118, Issue 12, December 2011, Pages 2374-2381
Ophthalmology

Original article
A Head-to-Head Comparison of 16 Cataract Surgery Outcome Questionnaires

https://doi.org/10.1016/j.ophtha.2011.06.008Get rights and content

Purpose

To investigate the responsiveness of 16 questionnaires used in cataract surgery outcomes.

Design

Prospective, observational study.

Participants

Patients at the Ophthalmology Eye Clinic, Flinders Medical Centre, Adelaide, Australia, and 1 matched eye clinic in Sweden.

Methods

Sixteen Rasch-scaled cataract surgery questionnaires were completed before and 6 months after surgery. These were: the Cataract Symptom Scale, 6 versions of the National Eye Institute Visual Function Questionnaire, the Quality of Life and Vision Function Questionnaire, the Cataract TyPE Specification, the Visual Activities Questionnaire, the Visual Disability Assessment (VDA), the Visual Function and Quality of Life questionnaire, the Visual Function Index, Catquest-9SF, the Visual Symptoms and Quality of Life questionnaire, and the Cataract Outcomes Questionnaire. Responsiveness was calculated with the effect size (ES) statistic (change in questionnaire score divided by pooled standard deviation of the preoperative and postoperative scores).

Main Outcome Measures

Questionnaire responsiveness to cataract surgery (ability to detect clinically important change).

Results

All 16 questionnaires and their subscales were responsive to cataract surgery, with visual functioning scales being more responsive than socioemotional scales and some subscales being less responsive. The largest ES was for the Catquest-9SF (1.45; 95% confidence interval [CI], 1.22–1.67), which was the only instrument with a mean and 95% CI of more than 1.0 (very large ES). Three measures had very large ESs and 95% CIs of more than 0.80 (large ES): the VDA (activity limitations and subscale) and the Cataract Outcomes Questionnaire, although their 95% CIs overlapped with a number of other instruments.

Conclusions

The Catquest-9SF is short and highly responsive to cataract surgery, and so is ideal for measuring visual functioning outcomes. Other instruments may be preferred to measure different constructs.

Financial Disclosure(s)

The author(s) have no proprietary or commercial interest in any materials discussed in this article.

Section snippets

Patients

Consecutive patients on the public waiting list to receive cataract surgery were mailed packs of questionnaires. Each mailed pack was organized with regard the questionnaires included, with each patient being sent a maximum of 5 questionnaires, with no more than 120 total questions, to manage respondent burden. Questionnaire order within the packs was rotated to even out any impact of fatigue on response quality. Therefore, each questionnaire was completed effectively by a different group of

Results

Demographic data were collected for all 16 questionnaires completed before and after surgery, with their associated statistical comparison shown in Table 1. The highest number of completed preoperative and postoperative questionnaires was for the VDA, with 134 patients, and the lowest was for the revised 8-item Visual Function Index, with 53 patients.

Table 2 shows the responsiveness of each questionnaire as measured by ES. There was an improvement in all the mean questionnaire scores from

Discussion

The main aim of this study was to determine which Rasch-scaled questionnaires for investigating cataract surgery outcomes are the most responsive. Responsiveness was assessed using the ES, which is a statistic that indicates a questionnaire's ability to detect clinically important changes over time, such as before and after cataract surgery.43 A cataract questionnaire with a high ES will be able to demonstrate an improvement easier compared with a questionnaire with a lower ES, and as such

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    Manuscript no. 2010-1684.

    Financial Disclosure(s): The author(s) have no proprietary or commercial interest in any materials discussed in this article.

    Supported in part by the National Health and Medical Research Council, Centre of Clinical Research Excellence, Canberra, Australia (grant no.: 264620). The sponsor or funding organization had no role in the design or conduct of this research.

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