| Name of the Instrument/Tool | European Scleroderma Study Group Activity Index (EScSG-AI) |
| First Description |
Valentini G, Bencivelli W, Bombardieri S, D'Angelo S, Della Rossa A, Silman AJ, Black CM, Czirjak L, Nielsen H, Vlachoyiannopoulos PG. European Scleroderma Study Group to define disease activity criteria for systemic sclerosis. III. Assessment of the construct validity of the preliminary activity criteria. Ann Rheum Dis. 2003 Sep;62(9):901-3. |
| Year | 2003 |
| Domains | |
| Concept of constructs | Disease activity |
| Population/Disease | Disease specific |
| Originally developed for | Systemic sclerosis |
| 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 | French, Dutch |
| REFERENCE IDENTIFICATION | |
| Author/s | Valentini G, Bencivelli W, Bombardieri S, D'Angelo S, Della Rossa A, Silman AJ, Black CM, Czirjak L, Nielsen H, Vlachoyiannopoulos PG. |
| Title | European Scleroderma Study Group to define disease activity criteria for systemic sclerosis. III. Assessment of the construct validity of the preliminary activity criteria. |
| Journal | Ann Rheum Dis |
| Year | 2003 |
| Vol | 62 |
| Num | 9 |
| Pages | 901-3 |
| Country | Italy |
| Language | English |
| Other references of interest | |
| Link | https://pubmed.ncbi.nlm.nih.gov/31422354/ |
| Brief Description |
Revised European Scleroderma Trials and Research Group Activity Index is the best predictor of short-term severity accrual. Assessment of the predictive value for short-term disease severity accrual of the EUSTAR-AI, as compared with those of the EScSG-AI and of known adverse prognostic factors. |
| Link | https://pubmed.ncbi.nlm.nih.gov/20236952/ |
| Brief Description |
Construct validity evaluation of the European Scleroderma Study Group activity index, and investigation of possible new disease activity markers in systemic sclerosis, Rheumatology. Evaluation of the construct validity of the European Scleroderma Study Group (EScSG) activity index and modifications proposal. |
| Link | https://pubmed.ncbi.nlm.nih.gov/33091259/ |
| Brief Description |
An Update of Outcome Measures in Systemic Sclerosis. Arthritis Care & Research. Review to update various outcome measurements in SSc that have been used in clinical trials and/or have testing characteristics published, such as reliability and sensitivity to change. |
| Instrument/Tool Translations References | |
| No other References. | |
| DEVELOPER CONTACT INFORMATION | |
| Correspondence to | Gabriele Valentini |
| gabriele.valentini@unicampania.it | |
| Address | Rampe Brancaccio 49, 80132 Napoli |
| Website | --- |
| Available | --- |
| Links | --- |
| DESCRIPTION OF THE INSTRUMENT | |
| Type Of Measure | Composite Index |
| Brief Description |
The EScSG-AI is an SSc-specific measure for all patients with SSc. It contains the following 10 variables: total skin score, scleredema, digital necrosis, arthritis, erythrocyte sedimentation rate, reduced carbon monoxide transfer factor, hypocomplementemia, and patient-reported skin, vascular, and cardiopulmonary changes. The index defines disease activity for SSc |
| Number of Items | 10 |
| Range | 0-10 |
| Responses options/scale |
No |
| Developed for | Research, Clinical practice |
| PRACTICAL APPLICATION | |
| Method of administration | Physician |
| Recommendations to score |
Each variable from 0.5 to 2. Total score ranges from 0 to 10. |
| Score Interpretation | Higher scores indicates higher disease activity |
| Cut-off points | A score of 3 or above indicates active disease. |
| Cut-off points applied to | --- |
| Smallest detectable change if described | --- |
| Smallest detectable change applied to | --- |
| Completion time by the patient | - minutes |
| Scoring time by the assessor | - minutes |
| Training to score | Not necessary |
| Strengths | Useful in clinical practice & research |
| Limitations | --- |
| OTHER COMMENTS | |
| Other Comments |
The EUSTAR-AI was developed from the charts of 97 patients in the European Scleroderma Trials and Research database and validated in 60 patients recruited from the same database. |