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. 2022 Feb 28;79(4):390–398. doi: 10.1001/jamaneurol.2021.5598

Table. Patient Demographics for All Included Studies and Each Specific Biomarkera.

Variable No. (%)
All studies NSE S100β GFAP Nf-L Tau UCH-L1
Included studies, No. 86 72 29 9 10 6 4
Study patients
Total No. 10 567 9880 3420 1055 1231 883 757
Men 7777 (73.6) 7319 (74.1) 2425 (70.9) 803 (76.1) 963 (78.2) 698 (79.0) 605 (79.9)
Women 2790 (26.4) 2561 (25.9) 995 (20.1) 252 (23.9) 268 (21.8) 185 (21.0) 152 (20.1)
Age, mean (SD), y 62.8 (10.2) 63.3 (11.1) 64.4 (9.1) 64.1 (12.7) 63.0 (12.6) 63.5 (13.0) 63.7 (12.3)
OHCA 8629 (89.6) 7952 (88.7) 2958 (87.5) 936 (88.7) 1191 (97.9) 860 (97.4) 754 (99.6)
Cardiac origin 4802 (69.4) 4352 (69.0) 993 (64.3) 827 (91.9) 919 (88.0) 162 (83.5) 727 (96.0)
Witnessed 4104 (76.9) 3869 (77.8) 939 (68.0) 776 (83.1) 254 (77.7) 49 (79.0) 649 (45.1)
Shockable ECG 5081 (52.5) 4814 (53.4) 1690 (51.9) 705 (66.8) 247 (63.7) 100 (51.5) 569 (39.5)
Bystander CPR 3426 (57.4) 3281 (59.0) 907 (53.7) 610 (69.2) 745 (70.0) 116 (67.4) 524 (36.4)
TTM 8070 (86.8) 7736 (88.1) 2381 (80.4) 970 (91.9) 967 (98.4) 802 (90.1) 751 (99.2)
Favorable outcome 4733 (44.8) 4466 (45.2) 1499 (43.8) 508 (48.2) 645 (52.4) 442 (50.1) 373 (49.3)
Outcome scale
CPC 67 (77.9) 57 (79.2) 20 (69.0) 7 (77.8) 8 (80.0) 6 (100) 4 (100)
GOS 7 (8.1) 7 (9.7) 4 (13.8) 1 (11.1) 0 0 0
mGOS 2 (2.3) 1 (1.4) 0 1 (11.1) 1 (10.0) 0 0
Survival 10 (11.6) 7 (9.7) 5 (17.2) 0 1 (10.0) 0 0
mRS 0 0 0 0 0 0 0

Abbreviations: CPC, cerebral performance category; CPR, cardiopulmonary resuscitation; ECG, electrocardiogram; GFAP, glial fibrillary acidic protein; GOS, Glasgow Outcome Scale; mGOS, Modified Glasgow Outcome Scale; mRS, modified Rankin Scale; Nf-L, neurofilament light; NSE, neuron-specific enolase; OHCA, out-of-hospital cardiac arrest; S100β, S100 calcium-binding protein β; TTM, targeted temperature management; UCH-L1, ubiquitin carboxyl hydrolase L1.

a

Not every study reported demographic data, such as OHCA or whether the arrest was of cardiac origin; therefore, the percentage values are based on the total sample size of only the studies that reported on each specific demographic factor. Furthermore, if multiple publications were included in the meta-analyses from the same trial (eg, TTM), their data were added to the relevant biomarker columns but were not duplicated within any single column (eg, total sample size did not duplicate patients from the same trial but different publications).