Parameter | APE | Nonmassive APE | Submassive APE | Massive APE |
Subjects n | 79 | 18 | 51 | 9 |
Age yrs | 63±17 | 52±20+ | 67±15* | 66±13 |
Females:males | 50:29 | 6:12 | 37:14* | 6:3 |
BPs mmHg | 123±23 | 132±21+ | 126±20 | 83±11#,¶ |
fc 1·s−1 | 101±22 | 98±24+ | 98±18 | 122±29#,¶ |
Sp,O2 % | 89±7 | 93±4+ | 88±7* | 85±8# |
RV:LV | 0.86±0.32 | 0.63±0.23+ | 0.90±0.29* | 1.21±0.42# |
Hypokinesis | 23 (29) | 0 | 19 (37)* | 4 (44)# |
TVPG mmHg | 43±13 | 28±8+ | 46±13* | 38±5# |
Deaths | 15 (19) | 0 | 10 (19.6) | 4 (44.4)# |
SAE | 24 (30) | 0 | 16 (31)* | 7 (78)# ,¶ |
Data are presented as mean±sd or n (%) unless otherwise stated
BPs: systolic blood pressure
fc: cardiac frequency
Sp,O2: pulsoximetry
RV/LV: right-to-left ventricle diameter ratio
TVPG: tricuspid valve pressure gradient
SAE: at least one in-hospital serious adverse event (death, cardiopulmonary resuscitation, thrombolysis, need for i.v. catecholamine infusion)
*: p<0.05 nonmassive versus submassive APE
#: p<0.05 nonmassive versus massive APE
¶: p<0.05 submassive versus massive APE
+: p<0.05 in analysis of variance (ANOVA) test or Kruskal-Wallis ANOVA test for three groups