Results

Between March 2021 and October 2022, a total of 21,139 patients met our inclusion criteria and were included the study. Upon propensity matching, 1,349 patients were included in the primary matched cohort (1,349 mAb-treated; 1,349 untreated). The propensity score matching diminished the imbalance in most of the key covariates, including age, race, immunosuppression, renal disorder, respiratory disorder, tobacco use, months into availability of mAb treatment, acuity level, and number of vaccinations. However, the propensity matched sample did differ significantly in months into mAb availability and number of COVID-19 vaccinations. Measures of association are available in Table 1.

Characteristics of the mAb patients in the primary cohort

In the propensity-matched cohort, mAb-treated patients reflected characteristics consistent with patients at a high risk for progression to severe COVID-19 (Table 1). Among patients who received mAb therapy (n = 1,349), 805 (60%) were aged 65 years or older, 387 (29%) were nonwhite, 136 (10%) were immunosuppressed, 275 (20%) suffered from renal disorders, and 452 (34%) suffered from respiratory disorders.

Table 1. Patient Characteristics and Covariate Balance Before and After Propensity Matching


Characteristic Before propensity matching After propensity matching
Treated, N = 1,3491 Untreated, N = 19,7901 p2 Treated, N = 1,3491 Untreated, N = 1,3491 p2
Male 636 (47%) 8,273 (42%) <0.001 636 (47%) 614 (46%) 0.4
Nonwhite 387 (29%) 7,743 (39%) <0.001 387 (29%) 367 (27%) 0.4
Age 65+ 805 (60%) 7,286 (37%) <0.001 805 (60%) 839 (62%) 0.2
Arrythmia 305 (23%) 3,150 (16%) <0.001 305 (23%) 296 (22%) 0.7
Cancer 186 (14%) 1,801 (9.1%) <0.001 186 (14%) 174 (13%) 0.5
Cardiovascular disease 777 (58%) 8,965 (45%) <0.001 777 (58%) 744 (55%) 0.2
Diabetes 250 (19%) 2,814 (14%) <0.001 250 (19%) 233 (17%) 0.4
Immunosuppressed 136 (10%) 603 (3.0%) <0.001 136 (10%) 140 (10%) 0.8
Obese 522 (39%) 8,679 (44%) <0.001 522 (39%) 537 (40%) 0.6
Renal disease 275 (20%) 2,460 (12%) <0.001 275 (20%) 255 (19%) 0.3
Respiratory disease 452 (34%) 7,040 (36%) 0.12 452 (34%) 412 (31%) 0.10
Tobacco user 47 (3.5%) 2,206 (11%) <0.001 47 (3.5%) 34 (2.5%) 0.14
Months since mAb approval 15 (5) 13 (5) <0.001 15 (5) 14 (5) 0.001
Acuity level <0.001 0.13
    1 5 (0.4%) 179 (0.9%) 5 (0.4%) 14 (1.0%)
    2 173 (13%) 3,168 (16%) 173 (13%) 156 (12%)
    3 923 (68%) 11,756 (59%) 923 (68%) 916 (68%)
    4 248 (18%) 4,687 (24%) 248 (18%) 263 (19%)
COVID vaccinations <0.001 0.040
    0 1,298 (96%) 18,256 (92%) 1,298 (96%) 1,299 (96%)
    1 14 (1.0%) 420 (2.1%) 14 (1.0%) 19 (1.4%)
    2 4 (0.3%) 408 (2.1%) 4 (0.3%) 8 (0.6%)
    3 9 (0.7%) 489 (2.5%) 9 (0.7%) 14 (1.0%)
    4 24 (1.8%) 217 (1.1%) 24 (1.8%) 9 (0.7%)
1 n (%); Mean (SD)
2 Pearson’s Chi-squared test; Wilcoxon rank sum test

Primary and secondary outcomes

The crude rates of rehospitalization, mortality, and inpatient outcomes are shown in Table 2. During the study period, the incidence of 28-day hospitalization in our primary matched cohort was 9.4% (n = 127/1,349) for untreated patients compared to 6.3% (n = 85/1,349) among mAb-treated patients. The mortality rate for untreated patients was 5.3% (n = 41/1,349) compared to 1.7% (n = 23/1,349) for mAb-treated patients. The rate of inpatient admission for untreated patients was 8.6% (n = 116/1,349) compared to 3.8% (n = 51/1,349) for mAb-treated patients. Rates of ICU and mechanical ventilation did not differ significantly by treatment group.

Table 2. Primary and Secondary Outcomes for Primary Matched Cohort


Characteristic Treated, N = 1,3491 Untreated, N = 1,3491 p2
Primary outcomes
28-Day Readmission 85 (6.3%) 127 (9.4%) 0.003
Mortality 23 (1.7%) 71 (5.3%) <0.001
Secondary outcomes
Any days as hospital inpatient 51 (3.8%) 116 (8.6%) <0.001
Any days in ICU 10 (0.7%) 20 (1.5%) 0.066
Any days on ventilator 4 (0.3%) 4 (0.3%) >0.9
1 n (%)
2 Pearson’s Chi-squared test

The adjusted analyses are presented in Table 3. Treatment with mAb was associated with reduced odds of 28-day rehospitalization (adjusted odds ratio [aOR] 0.66, [95% confidence interval (CI)] 0.49-0.87), P = 0.004). Mortality rates also differed significantly between the two groups. Treatment with mAb was associated with reduced odds of mortality (adjusted odds ratio [aOR] 0.32, [95% confidence interval (CI)] 0.19-0.51), P < 0.001). Treatment was also associated with reduced odds of inpatient admissions (adjusted odds ratio [aOR] 0.43, [95% confidence interval (CI)] 0.31-0.61), P < 0.001).1

Table 3. Adjusted Odds Ratios


Characteristic 28-Day Rehospitalization Mortality Inpatient
OR1 95% CI1 p OR1 95% CI1 p OR1 95% CI1 p
Received mAb 0.66 0.49, 0.87 0.004 0.32 0.19, 0.51 <0.001 0.43 0.31, 0.61 <0.001
Months since mAb approval 0.97 0.94, 1.00 0.038 0.96 0.92, 1.00 0.080 0.93 0.90, 0.96 <0.001
COVID vaccinations 1.16 0.90, 1.42 0.2 1.03 0.63, 1.44 >0.9 1.05 0.74, 1.37 0.8
1 OR = Odds Ratio, CI = Confidence Interval

  1. In these adjusted analyses, months since mAb approval of the first ED visit remained a statistically significant covariate after controlling for mAb treatment and number of COVID vaccinations. Months since mAb approval was associated with significantly but slightly reduced odds of rehospitalization (adjusted odds ratio [aOR] 0.97, [95% confidence interval (CI)] 0.94-1.00), P = 0.038) and inpatient admissions (adjusted odds ratio [aOR] 0.93, [95% confidence interval (CI)] 0.90-0.96), P < 0.001).↩︎