. | Patients . |
---|---|
Standardized endpoints (VARC-2) | |
Device success | |
All patients | 42/43 (98%) |
Patients with cardiogenic shock | 22/23 (98%) |
Patients with impaired LV or RV function, pulmonary hypertension with enlarged RV | 20/20 (100%) |
Safety <30 days | |
All patients | 34/43 (79%) |
Patients with cardiogenic shock | 15/23 (65%) |
Patients with impaired LV or RV function, pulmonary hypertension with enlarged RV | 19/20 (95%) |
Time of hospitalization (days) | |
Length of stay in intensive care unit | 3.2 (0.3–66) |
Total length of stay | 11.8 (2.7–103) |
Thirty-day mortality | |
All patients | 6 (14%) |
Patients with cardiogenic shock | 6 (28.6%) |
Patients with impaired LV or RV function, pulmonary hypertension with enlarged RV | No death |
Survival | |
Six-month survival | 60 ± 8% |
Patients with cardiogenic shock | 41 ± 11% |
Patients with impaired LV or RV function, or pulmonary hypertension with enlarged RV | 86 ± 9.5% |
One-year survival | 57 ± 8.4% |
Patients with cardiogenic shock | 36 ± 11% |
Patients with impaired LV or RV function, or pulmonary hypertension with enlarged RV | 86 ± 9.5% |
Two-year survival | 49 ± 10% |
Patients with cardiogenic shock | 36 ± 11% |
Patients with impaired LV or RV function, or pulmonary hypertension with enlarged RV | 68 ± 17% |
. | Patients . |
---|---|
Standardized endpoints (VARC-2) | |
Device success | |
All patients | 42/43 (98%) |
Patients with cardiogenic shock | 22/23 (98%) |
Patients with impaired LV or RV function, pulmonary hypertension with enlarged RV | 20/20 (100%) |
Safety <30 days | |
All patients | 34/43 (79%) |
Patients with cardiogenic shock | 15/23 (65%) |
Patients with impaired LV or RV function, pulmonary hypertension with enlarged RV | 19/20 (95%) |
Time of hospitalization (days) | |
Length of stay in intensive care unit | 3.2 (0.3–66) |
Total length of stay | 11.8 (2.7–103) |
Thirty-day mortality | |
All patients | 6 (14%) |
Patients with cardiogenic shock | 6 (28.6%) |
Patients with impaired LV or RV function, pulmonary hypertension with enlarged RV | No death |
Survival | |
Six-month survival | 60 ± 8% |
Patients with cardiogenic shock | 41 ± 11% |
Patients with impaired LV or RV function, or pulmonary hypertension with enlarged RV | 86 ± 9.5% |
One-year survival | 57 ± 8.4% |
Patients with cardiogenic shock | 36 ± 11% |
Patients with impaired LV or RV function, or pulmonary hypertension with enlarged RV | 86 ± 9.5% |
Two-year survival | 49 ± 10% |
Patients with cardiogenic shock | 36 ± 11% |
Patients with impaired LV or RV function, or pulmonary hypertension with enlarged RV | 68 ± 17% |
Data are presented as n/n, %, or estimate, standard error.
LV: left ventricular; RV: right ventricular.
. | Patients . |
---|---|
Standardized endpoints (VARC-2) | |
Device success | |
All patients | 42/43 (98%) |
Patients with cardiogenic shock | 22/23 (98%) |
Patients with impaired LV or RV function, pulmonary hypertension with enlarged RV | 20/20 (100%) |
Safety <30 days | |
All patients | 34/43 (79%) |
Patients with cardiogenic shock | 15/23 (65%) |
Patients with impaired LV or RV function, pulmonary hypertension with enlarged RV | 19/20 (95%) |
Time of hospitalization (days) | |
Length of stay in intensive care unit | 3.2 (0.3–66) |
Total length of stay | 11.8 (2.7–103) |
Thirty-day mortality | |
All patients | 6 (14%) |
Patients with cardiogenic shock | 6 (28.6%) |
Patients with impaired LV or RV function, pulmonary hypertension with enlarged RV | No death |
Survival | |
Six-month survival | 60 ± 8% |
Patients with cardiogenic shock | 41 ± 11% |
Patients with impaired LV or RV function, or pulmonary hypertension with enlarged RV | 86 ± 9.5% |
One-year survival | 57 ± 8.4% |
Patients with cardiogenic shock | 36 ± 11% |
Patients with impaired LV or RV function, or pulmonary hypertension with enlarged RV | 86 ± 9.5% |
Two-year survival | 49 ± 10% |
Patients with cardiogenic shock | 36 ± 11% |
Patients with impaired LV or RV function, or pulmonary hypertension with enlarged RV | 68 ± 17% |
. | Patients . |
---|---|
Standardized endpoints (VARC-2) | |
Device success | |
All patients | 42/43 (98%) |
Patients with cardiogenic shock | 22/23 (98%) |
Patients with impaired LV or RV function, pulmonary hypertension with enlarged RV | 20/20 (100%) |
Safety <30 days | |
All patients | 34/43 (79%) |
Patients with cardiogenic shock | 15/23 (65%) |
Patients with impaired LV or RV function, pulmonary hypertension with enlarged RV | 19/20 (95%) |
Time of hospitalization (days) | |
Length of stay in intensive care unit | 3.2 (0.3–66) |
Total length of stay | 11.8 (2.7–103) |
Thirty-day mortality | |
All patients | 6 (14%) |
Patients with cardiogenic shock | 6 (28.6%) |
Patients with impaired LV or RV function, pulmonary hypertension with enlarged RV | No death |
Survival | |
Six-month survival | 60 ± 8% |
Patients with cardiogenic shock | 41 ± 11% |
Patients with impaired LV or RV function, or pulmonary hypertension with enlarged RV | 86 ± 9.5% |
One-year survival | 57 ± 8.4% |
Patients with cardiogenic shock | 36 ± 11% |
Patients with impaired LV or RV function, or pulmonary hypertension with enlarged RV | 86 ± 9.5% |
Two-year survival | 49 ± 10% |
Patients with cardiogenic shock | 36 ± 11% |
Patients with impaired LV or RV function, or pulmonary hypertension with enlarged RV | 68 ± 17% |
Data are presented as n/n, %, or estimate, standard error.
LV: left ventricular; RV: right ventricular.
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