Table 3. Recipient Characteristics.
Track 2 N = 23 | Track 3 N = 12 | P Value± | |
---|---|---|---|
Age * | 61 (21.5) | 50.5 (11.25) | 0.054 |
Sex | 0.16 | ||
Male | 39.1% | 66.7% | |
Female | 60.9% | 33.3% | |
BMI * | 29.9 (12.06) | 27.3 (6.68) | 0.96 |
Race | 0.84 | ||
Caucasian | 17.4% | 25.0% | |
African American | 4.3% | 8.3% | |
Hispanic | 60.9% | 58.3% | |
Asian | 17.4% | 8.3% | |
Days from symptom onset to treatment * | 10 (10.5) | 16 (9.5) | 0.0063 |
Day 10 COVID swab PCR^ | 0.6 | ||
Positive | 54.5% | 10.0% | |
Negative | 45.5% | 30.0% | |
Not Determined | 60.0% | ||
Day 30 survival status | 0.015 | ||
Alive | 82.6% | 58.3% | |
Fatal | 17.4% | 41.7% | |
Intubated after treatment | |||
Yes | 17.4% | NA | |
No | 82.6% | NA | |
Days from infusion to discharge or death * | 8 (9) | 10 (7) | 0.062 |
Developed ARDS | 52.2% | 100% | 0.0055 |
Developed End Organ Dysfunction | 21.7% | 50.0% | 0.13 |
Concomitant Treatment | |||
Hydroxychloroquine | 69.6% | 91.7% | 0.22 |
Azithromycin | 52.2% | 75% | 0.28 |
Doxycycline or other antibiotic | 56.5% | 50% | 0.74 |
Steroids | 52.2% | 100% | 0.0055 |
Tociluzumab | 17.4% | 58.3% | 0.022 |
Remdesivir | 4.3% | 8.3% | 1 |
Comorbidities | |||
Hypertension | 47.8% | 33.3% | 0.49 |
Diabetes | 34.8% | 50.0% | 0.48 |
Heart Failure or CAD | 4.3% | 0% | 1 |
History of Smoking | 17.4% | 16.7% | 0.51 |
Lung disease or Asthma | 26.1% | 8.3% | 0.38 |
Immunocompromised | 30.4% | 8.3% | 0.22 |
Active Cancer | 26.1% | 8.3% | 0.38 |
*Median (IQR)
^Track 2, n = 22; Track 3, n = 10
±Continuous variables were analyzed using T-test; Categorical values were analyzed using Fisher’s exact test