Performance of self-reported best practice procedure components for CMS facilities (n=22)
Best practice | Non-CREST participants (%) (n=19) | CREST participants (%) (n=3) |
mRS pre-stent | 32 | 67 |
NIHSS pre-stent | 74 | 100 |
DSA including head and neck pre-stent | 74 | 100 |
Electronic calliper determination of per cent stenosis | 21 | 100 |
Measure per cent stenosis using NASCET criteria | 63 | 100 |
Embolic protection device use | 90 | 100 |
DSA including head and neck post-stent | 68 | 100 |
Treated with antiplatelet dual regimen | 79 | 100 |
ACT >250 s | 47 | 100 |
NIHSS 24 hours post-stent | 74 | 100 |
~30-day post-stent neurological assessment | 79 | 100 |
~30-day post-stent follow-up mRS | 58 | 100 |
~30-day post-stent follow-up NIHSS | 58 | 100 |
~30-day post-stent outcomes stroke and death | 68 | 100 |
~30-day non-invasive study | 58 | 67 |
Benchmark for stroke and death | 42 | 100 |
Overall | 62 | 100 |
ACT, activated clotting time; CMS, Centers for Medicare and Medicaid Services; CREST, Carotid Revascularisation and Medical Management for Asymptomatic Carotid Stenosis Study Trial; DSA, digital subtracted angiography; mRS, Modified Rankin Scale; NASCET, North American Symptomatic Carotid Endarterectomy Trial; NIHSS, National Institute of Health Stroke Scale.