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The patient reported intraocular lens questionnaire (PR-ILQ): content validity, psychometric performance, and use in a regulated clinical trial to evaluate safety and effectiveness outcomes
by
Moreno-Koehler, Alejandro
, Chacko, Jimmy
, Litcher-Kelly, Leighann
, Shields, Alan L.
, Galipeau, Nina
in
Aged
/ Aged, 80 and over
/ Cataracts
/ Clinical trials
/ Clinical Trials as Topic
/ Content validity
/ FDA approval
/ Female
/ Focus groups
/ Humans
/ Intraocular lens (iol) replacement
/ Intraocular lenses
/ Lenses, Intraocular - adverse effects
/ Male
/ Medical equipment
/ Medicine
/ Medicine & Public Health
/ Middle Aged
/ Ophthalmology
/ Patient reported intraocular lens questionnaire (pR-ILQ)
/ Patient Reported Outcome Measures
/ Patient Satisfaction
/ Patient-reported outcomes (PROs)
/ Product reviews
/ Psychometric performance
/ Psychometrics
/ Quality of Life Research
/ Quantitative psychology
/ Questionnaires
/ Reproducibility of Results
/ Surveys and Questionnaires - standards
/ Visual acuity
2025
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The patient reported intraocular lens questionnaire (PR-ILQ): content validity, psychometric performance, and use in a regulated clinical trial to evaluate safety and effectiveness outcomes
by
Moreno-Koehler, Alejandro
, Chacko, Jimmy
, Litcher-Kelly, Leighann
, Shields, Alan L.
, Galipeau, Nina
in
Aged
/ Aged, 80 and over
/ Cataracts
/ Clinical trials
/ Clinical Trials as Topic
/ Content validity
/ FDA approval
/ Female
/ Focus groups
/ Humans
/ Intraocular lens (iol) replacement
/ Intraocular lenses
/ Lenses, Intraocular - adverse effects
/ Male
/ Medical equipment
/ Medicine
/ Medicine & Public Health
/ Middle Aged
/ Ophthalmology
/ Patient reported intraocular lens questionnaire (pR-ILQ)
/ Patient Reported Outcome Measures
/ Patient Satisfaction
/ Patient-reported outcomes (PROs)
/ Product reviews
/ Psychometric performance
/ Psychometrics
/ Quality of Life Research
/ Quantitative psychology
/ Questionnaires
/ Reproducibility of Results
/ Surveys and Questionnaires - standards
/ Visual acuity
2025
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The patient reported intraocular lens questionnaire (PR-ILQ): content validity, psychometric performance, and use in a regulated clinical trial to evaluate safety and effectiveness outcomes
by
Moreno-Koehler, Alejandro
, Chacko, Jimmy
, Litcher-Kelly, Leighann
, Shields, Alan L.
, Galipeau, Nina
in
Aged
/ Aged, 80 and over
/ Cataracts
/ Clinical trials
/ Clinical Trials as Topic
/ Content validity
/ FDA approval
/ Female
/ Focus groups
/ Humans
/ Intraocular lens (iol) replacement
/ Intraocular lenses
/ Lenses, Intraocular - adverse effects
/ Male
/ Medical equipment
/ Medicine
/ Medicine & Public Health
/ Middle Aged
/ Ophthalmology
/ Patient reported intraocular lens questionnaire (pR-ILQ)
/ Patient Reported Outcome Measures
/ Patient Satisfaction
/ Patient-reported outcomes (PROs)
/ Product reviews
/ Psychometric performance
/ Psychometrics
/ Quality of Life Research
/ Quantitative psychology
/ Questionnaires
/ Reproducibility of Results
/ Surveys and Questionnaires - standards
/ Visual acuity
2025
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The patient reported intraocular lens questionnaire (PR-ILQ): content validity, psychometric performance, and use in a regulated clinical trial to evaluate safety and effectiveness outcomes
Journal Article
The patient reported intraocular lens questionnaire (PR-ILQ): content validity, psychometric performance, and use in a regulated clinical trial to evaluate safety and effectiveness outcomes
2025
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Overview
Background
Patient-reported outcomes (PROs) are underutilized in medical device evaluations, including in ophthalmology and intraocular lens (IOL) replacements. This article summarizes research conducted to develop the Patient-Reported Intraocular Lens Questionnaire (PR-ILQ) and support its content validity and psychometric performance. Use of the PR-ILQ in a regulated clinical trial to support new product approval decisions, secondary effectiveness claims, and safety observations is also discussed.
Results
The PR-ILQ, developed with ophthalmology experts (
n
= 10) and use of qualitative data generated from patients during concept elicitation (
n
= 44) and cognitive debriefing (
n
= 32) interviews, includes the Vision Correction Scale (VCS, three items), Vision Disturbance Scale (VDS, eight items), and IOL Replacement Satisfaction Scale (IOL-RSS, five items). Each assessment is distinct, and items within each are scored independently to address treatment benefit hypotheses. With its content validity established, the PR-ILQ was administered to 271 subjects (mean age = 68.3 years) participating in a clinical trial to evaluate the safety and effectiveness of an asymmetric segmented multifocal IOL (SBL-INI-02–13). Descriptively, item scores behaved as expected, with clustering of VCS and VDS scores at more- and less-severe levels at study entry and exit, respectively, though scores were distributed across response options across timepoints. Test-retest reliability results mostly indicate “fair”/“good” (weighted Kappa [KW]/intraclass correlation coefficient [ICC] > 0.40 to 0.60) to “excellent” (KW/ICC > 0.75) reproducibility for VCS, VDS, and IOL-RSS items in two independent analyses. Construct validity hypotheses, including those associated with sensitivity to change, were supported via correlational analysis showing a pattern of expected relationships among PR-ILQ items and with other variables including ratings of visual acuity. For example, reduced use of vision correction at near (
r
= −0.28), intermediate (
r
= −0.42), and far (
r
= −0.57) distances were more strongly related to overall lens satisfaction at end of study than improved visual acuity at those same distances (
r
= −0.25. −0.26, and −0,14).
Conclusions
The PR-ILQ is content valid and early evidence suggests it is capable of producing reliable scores upon which valid conclusions may be drawn when administered among patients undergoing cataract lens replacement surgery. Acknowledging limitations and need for additional psychometric evaluation, the assessment recently supported a new product approval decision, secondary effectiveness claims, and safety observations. Together, this indicates that the PR-ILQ, along with the evidentiary basis and suggestions for use presented herein, will be of immediate value to IOL replacement outcomes researchers, regulators, and other stakeholders interested in generating evidence to inform health care decisions and improving cataracts patients’ lives.
Trial registration
Clinicaltrials.gov, NCT02487160. Registered 25 June 2015,
https://clinicaltrials.gov/study/NCT02487160
.
Publisher
Springer International Publishing,Springer Nature B.V,Springer,SpringerOpen
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