PROM Detail

Health Utilities Index
  • Basic Information
  • Detailed Information
  • Domains
  • Psychometrics

Basic Information

Abbreviated name
HUI3
Full name
Health Utilities Index
Items ?
The number of questions in the survey
15
Short description
HUI refers to both HUI Mark 2 (HUI2) and HUI Mark 3 (HUI3) instruments. The classification systems provide compact but comprehensive frameworks within which to describe health status. The multi-attribute utility functions provide all the information required to calculate single-summary scores of health-related quality of life (HRQL) for each health state defined by the classification systems. HUI provides comprehensive, reliable, responsive and valid measures of health status and HRQL for subjects in clinical studies.
PCCC or QoL? ?
This compendium contains patient-reported measures that are either designed to specifically measure aspects of Person Centred Co-Ordinated Care (P3C), or alternatively tools that are designed to measure some aspect of Quality of Life (QoL) or Health Related Quality of Life (hrQoL). All the measures in this compendium have been broadly categorised into one of those two concepts.
Quality of Life
Main Domains Measured ?
This is the key domains that the measure is targeting.
Health status, self-assessment
Type of measure ?
The measures in this compendium can take a variety of forms. Generally, they will be either Patient Reported Outcome Measure (PROM) or Patient Reported Experience Measure (PREM). However, we have also included a few measures that are completed by proxy-individual (PROXY), which are useful in instances where the respondent cannot answer directly (e.g. dementia or end of life). Sometimes, these measures can even be a composite of these types, and target both experiences and outcomes – we have labelled these measures “PROEMs”.
PROM
Respondent ?
The person that fills in the questionnaire - e.g. patient, Health Care Professional, or proxy (normally a carer or family member)
Patients
Permissive licence ?
Whether the measure is free to use without major restrictions, or instead permission and/or licensing fees are required. E.g. if "Yes", you should seek authorisation/permission prior to using the instrument.
No

Detailed Information

Year developed ?
The year in which the measure was first published.
2003
Country developed in ?
The main country[s] in which the measure was first developed.
Canada
Website link ?
A link to the developer of the measure, if they have a website.
Target condition ?
The measures can be either generic or disease specific (e.g. Diabetes, Heart Failure)
Generic
Main context tested in ?
The main context in which the measure has been developed and used (E.g. Hopital, General Practice etc).
Clinical settings
Main countries used in ?
The main countries in which the measure has been developed and used.
Numerous
Target age ?
e.g. Adults, Children, Elderly
Adults, aged adults
Main uses of measure ?
The context in which the measure is most often used – e.g. clinical trials; national surveys.
HUI was designed to provide comprehensive, reliable, responsive and valid measures of health status and HRQL for subjects in clinical studies.
Impact ?
A crude indication of the impact of the measure on academia. This is the number of times the original publication has been cited on PubMed, divided/normalised to the years since publication.
11.46153846
Language
English
Official translations
40 different translations
Other versions available
Over 250 versions available
Flesch-Kincaid readability tests ?
A rating that corresponds approximately to US school grade level. For example, a score of 8.0 means that an eighth grader can understand the document. Generally, a score of 7 or 8 should be appropriate.
7.4
Time to complete
10

Domains

Domain description
Health status, self-assessment
100%
80%
60%
40%
20%
0%
8
3
4
Physical health symptoms
Physical health function
Mental health

Psychometrics

CTT or IRT ?
Whether the measure uses Classical Test Theory, or the newer Item Response Theory
CTT
COSMIN/Terwee/EMPRO/OXFORD ?
This is the method used to systematically review the psychometric properties of the instrument - either the COSMIN criteria, Terwee's criteria, EMPRO, or the custom methodology of the Oxford PROMS group.
Setting ?
This the setting in which the psychometrics were evaluated. This field also contains a link to the original study where the systematic ratings (showing in the diagram to the right) of the psychometric data was performed. The data given below is for indicative purposes only, and users should refer to the original source when seriously reviewing measures.
Internal consistency ?
Internal consistency evaluates how individual items of the outcome measure correlate with each other. The quality criteria to assess internal consistency is Cronbach’s alpha, which reports the average of correlations between all possible halves of the scale. A high internal consistency (>0.8) suggests that many items of the measure are capturing similar aspects. Internal consistency is important if an outcome measure is used to monitor a single underlying concept with multiple items. However, if the underlying clinical phenomenon is complex, internal consistency is not so relevant or may be reported as sub-scales of the instrument.
Reliability ?
The reliability of an outcome measure refers to whether the measure produces the same or similar results when administered in unchanged conditions. Reliability is important as it can reduce measurement error or errors that are related to the process of measurement. Providing clear definitions for the scores from an outcome measure helps to make it more reliable. Fewer points on the scale also improves reliability. It can be assessed via inter-rater reliability (whether similar results are reached when different observers are used to rate the same situation or patient) or rest-retest reliability (whether similar results are reached over two distinct periods of time in unchanged conditions).
Measurement error ?
The difference between a measured value of quantity and its true value.
Content validity ?
Validity is one of the most important aspects of an outcome measure. It refers to what a tool is measuring and whether it is measuring what it should be measuring.
Construct structural validity ?
Construct validity is the extent to which a measurement corresponds to the theoretical concepts or constructs that it was designed to measure. It can be assessed via statistical evaluations of the structure of the measurement, such as factor analysis. Correlations that fit the expected pattern contribute evidence of construct validity.
Construct hypothesis testing ?
If no other measure or gold standard exists for comparison, the measure could be linked to a theory or hypothesis in order to show construct validity.
Construct cross cultural validity ?
To be able to use outcome measures with different groups to compare results between countries, outcome measures need to be translated into other languages by following a formal process and the same rigorous validation process also applies as for the original measure. Even though this is lengthy and costly, it is an important procedure to ensure accurate scores when outcome measures are used and compared.
Criterion validity ?
Criterion validity refers to whether the measure correlates with another instrument that measures similar aspects. Preferably, the other instrument is the ‘gold standard’, meaning it has been validated, and is widely used and accepted in the field.
Responsiveness ?
Responsiveness to change refers to whether the measure can detect clinically important changes over time that are related to the course of the disease or to an intervention, such as symptom management.
Interpretability ?
The interpretability of an outcome measure refers to whether the results (which are often a number) can be translated into something more meaningful to the patient, the family or clinician. An interpretable tool should enable a response to these questions: What is severe? What is the cut-off point when the outcome measure is used for diagnosis? How many points correlate with a symptom change?
Floor ceiling effects ?
Floor and ceiling effects occur when scores from an outcome measure are not discriminated below or above a certain level (meaning that they will not detect change). This can be a particular problem in conditions with a very wide range of symptoms.
COSMIN
0
0
0
0
0
0
0
0

About psychometric information: The above information on the psychometric properties of the questionnaire are for guideline purposes only.  They were, however, derived from a systematic review of measurement properties for this tool.  You can find the original study above, when clicking on the “setting” field. To derive a consistent scoring system from various different types of studies, we often had to re-map scores/categories, so that the information above may not accurately reflect the original source.  Please refer to original references for complete information.

Key: 0-3 scoring system:
Empty = study did not assess this evidence
-1 = negative data
0 = conflicting/no data
1: Weak evidence
2: Moderate evidence
3: Strong evidence
-1
0
1
2
3