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. 2022 May 9;9:893273. doi: 10.3389/fmed.2022.893273

TABLE 2.

PLASMIC score, ADAMTS13 activity, and distribution of clinical diagnoses.

PLASMIC score risk prediction (n = 24)
Low riska
(n = 6)
Intermediate riskb
(n = 8)
High riskc
(n = 10)
ADAMTS13 activity
≤10%, n (%)
0 0 9 (90)
ADAMTS13 activity
>10%, n (%)
6 (100) 8 (100) 1 (10)
Clinical diagnosis, n (%)
TTP 0 0 9 (90)
Other TMA
aHUS 0 1 (12.5) 0
SLE-associated TMA 1 (16.7) 4 (50) 0
DI-TMA 2 (33.3) 0 0
TA-TMA 2 (33.3) 0 0
Malignant hypertension 0 1 (12.5) 0
Unexplained TMA 1(16.7) 2 (25) 0
Malignancy 0 0 1(10)

aLow risk: PLASMIC score of 0–4.

bIntermediate risk: PLASMIC score of 5.

cHigh risk: PLASMIC score of 6–7.

ADAMTS13, a disintegrin and metalloprotease with thrombospondin type 1 repeats, member 13; TTP, thrombotic thrombocytopenic purpura; TMA, thrombotic microangiopathy; aHUS, atypical hemolytic uremic syndrome; SLE, systemic lupus erythematosus; DI-TMA, drug-induced thrombotic microangiopathy; TA-TMA, transplant-associated thrombotic microangiopathy.