Detailled Information

Name of the Instrument/Tool Lupus Impact Tracker (LIT)
First Description

Jolly M, Garris CP, Mikolaitis RA, Jhingran PM, et al. Development and validation of the Lupus Impact Tracker: a patient-completed tool for clinical practice to assess and monitor the impact of systemic lupus erythematosus. Arthritis Care Res (Hoboken). 2014 Oct;66(10):1542-50. 

Year 2014
Domains
Concept of constructs Health related quality of life
Population/Disease Disease specific
Originally developed for Systemic Lupus Erythematosus (SLE)
Other rheumatic diseases
where can be applied (only if validated)
---
Additional population with no rheumatic diseases No
Language: Originally published in English
Available in Language Spanish, French, German, Swedish, Italian
REFERENCE IDENTIFICATION
Author/s Jolly M, Garris CP, Mikolaitis RA, Jhingran PM, Dennis G, Wallace DJ, Clarke A, Dooley MA, Parke A, Strand V, Alárcon GS, Kosinski M
Title Development and validation of the Lupus Impact Tracker: a patient-completed tool for clinical practice to assess and monitor the impact of systemic lupus erythematosus.
Journal Arthritis Care Res (Hoboken)
Year 2014
Vol 66
Num 10
Pages 1542-50
Country USA
Language English
Other references of interest
Link https://pubmed.ncbi.nlm.nih.gov/26814452/
Brief Description

Prospective Validation of the Lupus Impact Tracker: A Patient-Completed Tool for Clinical Practice to Evaluate the Impact of Systemic Lupus Erythematosus

Link https://pubmed.ncbi.nlm.nih.gov/27587460/
Brief Description

The lupus impact tracker is responsive to changes in clinical activity measured by the systemic lupus erythematosus responder index

Link https://pubmed.ncbi.nlm.nih.gov/33091273/
Brief Description

Health-Related Quality of Life Measures in Adult Systemic Lupus Erythematosus

Instrument/Tool Translations References
Link https://pubmed.ncbi.nlm.nih.gov/28204765/
Brief Description

Cross-cultural validation of Lupus Impact Tracker in five European clinical practice settings

DEVELOPER CONTACT INFORMATION
Correspondence to Meenakshi Jolly
E-Mail meenakshi_Jolly@rush.edu
Address 1611 W Harrison St, Orthopedic Building Suite 510 Chicago, IL, 60612
Website ---
Available ---
Links ---
DESCRIPTION OF THE INSTRUMENT
Type Of Measure Scale
Brief Description

The LIT is a brief disease-specific instrument used to assess and monitor the impact of SLE on QoL.

Items for the LIT were selected using psychometric, clinimetric, and focus group methods from the LupusPRO, a validated patient-reported outcomes measure. Items include concentration, medication side effects, fulfilling family responsibilities, feelings of being worn out upon waking, bodily pain and aching, limitation of activities due to pain/fatigue, anxiety, depression, self-consciousness related to physical appearance, and ability to plan activities.

Number of Items 10
Range 0-100
Responses options/scale Yes
Five-point Likert scale
Developed for Research, Clinical practice
PRACTICAL APPLICATION
Method of administration Self-administered
Recommendations to score

Patients rank individual items on a scale of 0 to 4, and an overall score ranging from 0 to 100 is derived via a multiplication factor of 2.5. Normative data are not available.

Score Interpretation Higher scores indicate greater negative impact of SLE
Cut-off points ---
Cut-off points applied to ---
Smallest detectable change if described ---
Smallest detectable change applied to ---
Completion time by the patient <2 minutes
Scoring time by the assessor - minutes
Training to score Not necessary
Strengths Useful in clinical practice & research, Widely used
Limitations ---
OTHER COMMENTS
Other Comments

The characteristics of the validation cohorts included a disease duration of approximately 13 years, mean SLEDAI scores ranging from 3.9 to 6.4, and a mean SDI score of 1.0.