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Table 1 Number (percentage) of patients with TTM, survival to ICU discharge, and good neurological outcomes (Cerebral Performance Category score 1 or 2) according to presence of non-inclusion criteria for the HYPERION trial in patients comatose after cardiac arrest in non-shockable rhythm, due to any cause

From: Insights from patients screened but not randomised in the HYPERION trial

Characteristics

TTM

ICU survival

Good neurological outcome at ICU dischargea

Good neurological outcome on day 90a

No-flow > 10 min (n = 234)

76/234 (32.5%)

10/234 (4.3%)

5/233 (2.1%)

5/233 (2.1%)

Low-flow > 60 min (n = 35)

7/35 (20.0%)

2/35 (5.7%)

1/35 (2.8%)

1/35 (2.8%)

Haemodynamic instability (defined as norepinephrine > 1 µg/kg/min) (n = 120)

23/120 (19.2%)

21/120 (17.5%)

16/120 (13.3%)

16/120 (13%)

Time from cardiac arrest to screening > 300 min (n = 141)

26/140 (18.6%)

48/141 (34.0%)

33/140 (23.6%)

32/140 (22.8%)

Moribund (n = 291)

76/291 (26.1%)

10/289 (3.4%)

9/289 (3.1%)

9/289 (3.1%)

Cirrhosis Child–Pugh C (n = 7)

3/7 (42.8%)

2/7 (28.6%)

1/6 (16.6%)

1/6 (16.6%)

Pregnant or breastfeeding (n = 1)

0/1 (0%)

0/1 (0%)

0/1 (0%)

0/1 (0%)

Inclusion in another study (n = 3)

2/3 (66.6%)

1/3 (33.3%)

0/2 (0%)

0/2 (0%)

High risk of bleeding (n = 5)

2/5 (40.0%)

1/5 (20.0%)

1/5 (20%)

1/5 (20%)

Logistical reasonb (n = 307)

126/305 (41.3%)

112/307 (36.5%)

97/303 (32.0%)

93/299 (31.1%)

  1. TTM targeted temperature management, ICU intensive care unit
  2. aThe denominator decreased for some variables because data were unavailable in medical charts or patients could not be contacted by phone
  3. bLogistical reasons included unavailability of an investigator or of the randomisation software