Subgroups | n | Severe adverse events*, n (%) | Sensitivity, % (95% CI) | Specificity, % (95% CI) | PPV, % (95% CI) | NPV, % (95% CI) | PLR (95% CI) | NLR (95% CI) | AUROC (95% CI) |
---|---|---|---|---|---|---|---|---|---|
Patients without potential treatment restriction†| 342 | 57 (16.7) | 91.2 (81.1–96.2) | 70.5 (65.0–75.5) | 38.2 (30.5–46.6) | 97.6 (94.4–99.0) | 3.1 (2.5–3.8) | 0.1 (0.1–0.3) | 0.89 (0.84–0.94) |
CAP excluding HCAP‡ | 437 | 71 (16.2) | 94.4 (86.4–97.8) | 65.0 (60.0–69.7) | 34.3 (28.1–41.3) | 98.4 (95.8–99.4) | 2.7 (2.3–3.1) | 0.1 (0.0–0.2) | 0.88 (0.84–0.92) |
HCAP§ | 206 | 49 (23.8) | 87.8 (75.8–94.3) | 48.4 (40.7–56.2) | 34.7 (26.9–43.4) | 92.7 (84.9–96.6) | 1.7 (1.4–2.0) | 0.3 (0.1–0.5) | 0.78 (0.70–0.85) |
Patients without requirement of invasive MV/VS at admission|| | 629 | 106 (16.9) | 91.5 (84.7–95.5) | 60.0 (55.8–64.2) | 31.7 (26.7–37.1) | 97.2 (95.0–98.5) | 2.3 (2.0–2.6) | 0.1 (0.1–0.3) | 0.84 (0.80–0.88) |
Patients without immunosuppression** | 585 | 105 (17.9) | 91.4 (84.5–95.4) | 60.0 (56.0–64.7) | 33.6 (28.3–39.2) | 97.0 (94.4–98.4) | 2.3 (2.0–2.6) | 0.1 (0.1–0.3) | 0.84 (0.80–0.88) |