Table 5.
Measurements of Adverse Events | Total Patients (N=7019) | Hospital's Risk‐Standardized Occurrence Rate of Adverse Events for Which Patients Were at Risk by Tertiles (%) | ||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
First Tertile (1.35–2.82) | Second Tertile (2.83–4.44) | Third Tertile (4.45–19.28) | ||||||||||
No. of Patients at Risk | Adverse Event Rate | No. of Patients at Risk | Adverse Event Rate | No. of Patients at Risk | Adverse Event Rate | No. of Patients at Risk | Adverse Event Rate | |||||
n | % | % (95% CI) | n | % | % (95% CI) | n | % | % (95% CI) | n | % | % (95% CI) | |
Adverse drug events | ||||||||||||
Adverse events associated with digoxin | 353 | 5.0 | 1.7 (0.6–3.7) | 131 | 5.2 | 0.0 (0.0–2.7) | 106 | 4.7 | 1.9 (0.2–6.7) | 116 | 5.2 | 3.5 (1–8.7) |
Adverse events associated with hypoglycemic agents | 2853 | 40.6 | 10.5 (9.4–11.7) | 916 | 36.5 | 2.3 (1.4–3.5) | 900 | 39.5 | 10.0 (8.1–12.2) | 1037 | 46.4 | 18.2 (15.9–20.7) |
Adverse events associated with IV heparin | 2253 | 32.1 | 11.4 (10.1–12.8) | 641 | 25.6 | 2.0 (1.1–3.4) | 711 | 31.2 | 7.3 (5.5–9.5) | 901 | 40.3 | 21.3 (18.7–24.1) |
Adverse events associated with low‐molecular‐weight heparin and factor Xa inhibitor | 3156 | 45.0 | 5.2 (4.4–6.0) | 1216 | 48.5 | 0.6 (0.2–1.2) | 1032 | 45.3 | 4.3 (3.1–5.7) | 908 | 40.7 | 12.3 (10.3–14.7) |
Adverse events associated with warfarin | 669 | 9.5 | 6.3 (4.6–8.4) | 203 | 8.1 | 1.0 (0.1–3.5) | 232 | 10.2 | 5.2 (2.7–8.9) | 234 | 10.5 | 12.0 (8.1–16.8) |
General events | ||||||||||||
Hospital‐acquired pressure ulcers | 7019 | 100.0 | 5.4 (4.9–6) | 2507 | 100.0 | 1.6 (1.2–2.2) | 2279 | 100.0 | 5.0 (4.2–6) | 2233 | 100.0 | 10.0 (8.8–11.4) |
Inpatient falls | 7019 | 100.0 | 0.8 (0.6–1.0) | 2507 | 100.0 | 0.2 (0.1–0.5) | 2279 | 100.0 | 0.8 (0.5–1.3) | 2233 | 100.0 | 1.4 (1–2) |
Hospital‐acquired infections | ||||||||||||
Hospital‐acquired antibiotic‐associated Clostridium difficile | 3150 | 44.9 | 0.7 (0.4–1.0) | 1051 | 41.9 | 0.0 (0.0–0.4) | 1009 | 44.3 | 0.7 (0.3–1.4) | 1090 | 48.8 | 1.3 (0.7–2.2) |
Central line‐associated bloodstream infection | 863 | 12.3 | 1.0 (0.5–2.0) | 151 | 6.0 | 0.0 (0.0–2.4) | 268 | 11.8 | 0.7 (0.1–2.7) | 444 | 19.9 | 1.6 (0.6–3.2) |
Catheter‐associated urinary tract infection | 2471 | 35.2 | 5.9 (5–6.9) | 776 | 31.0 | 2.3 (1.4–3.6) | 803 | 35.2 | 4.5 (3.2–6.2) | 892 | 39.9 | 10.2 (8.3–12.4) |
Hospital‐acquired methicillin‐resistant Staphylococcus aureus | 6845 | 97.5 | 0.1 (0–0.2) | 2447 | 97.6 | 0.0 (0.0–0.2) | 2213 | 97.1 | 0.0 (0.0–0.2) | 2185 | 97.9 | 0.3 (0.1–0.6) |
Hospital‐acquired vancomycin‐resistant Enterococcus | 7002 | 99.8 | <0.01 (0.0–0.1) | 2504 | 99.9 | 0.0 (0.0–0.2) | 2270 | 99.6 | 0.0 (0.0–0.2) | 2228 | 99.8 | 0.0 (0.0–0.2) |
Postoperative Pneumonia | 431 | 6.1 | 7.4 (5.1–10.3) | 44 | 1.8 | 0.0 (0.0–8) | 119 | 5.2 | 3.4 (0.9–8.4) | 268 | 12.0 | 10.4 (7.1–14.8) |
Ventilator‐associated pneumonia | 229 | 3.3 | 11.4 (7.6–16.2) | 32 | 1.3 | 0.0 (0.0–10.9) | 64 | 2.8 | 3.1 (0.4–10.8) | 133 | 6.0 | 18.0 (11.9–25.7) |
Postprocedural events | ||||||||||||
Adverse events associated with femoral artery puncture for catheter angiographic procedures | 2808 | 40.0 | 2.6 (2–3.2) | 657 | 26.2 | 0.5 (0.1–1.3) | 909 | 39.9 | 2.2 (1.4–3.4) | 1242 | 55.6 | 3.9 (2.9–5.2) |
Adverse events associated with hip joint replacement | 3 | <0.01 | 66.7 (9.4–99.2) | 0 | 0.0 | N/A | 0 | 0.0 | N/A | 3 | 0.1 | 66.7 (9.4–99.2) |
Adverse events associated with knee joint replacement | 0 | 0.0 | N/A | 0 | 0.0 | N/A | 0 | 0.0 | N/A | 0 | 0.0 | N/A |
Contrast nephropathy associated with catheter angiography | 2828 | 40.3 | 13.8 (12.5–15.1) | 659 | 26.3 | 2.4 (1.4–3.9) | 919 | 40.3 | 10.2 (8.3–12.4) | 1250 | 56.0 | 22.3 (20–24.7) |
Mechanical complications associated with central lines | 1087 | 15.5 | 3.3 (2.3–4.6) | 201 | 8.0 | 0.0 (0.0–1.8) | 351 | 15.4 | 2.0 (0.8–4.1) | 535 | 24.0 | 5.4 (3.7–7.7) |
Postoperative cardiac events (cardiac and noncardiac surgeries) | 465 | 6.6 | 3.4 (2–5.5) | 50 | 2.0 | 0.0 (0.0–7.1) | 127 | 5.6 | 2.4 (0.5–6.8) | 288 | 12.9 | 4.5 (2.4–7.6) |
Postoperative venous thromboembolic event | 465 | 6.6 | 0.6 (0.1–1.9) | 50 | 2.0 | 0.0 (0.0–7.1) | 127 | 5.6 | 0.8 (0–4.3) | 288 | 12.9 | 0.7 (0.1–2.5) |
All events | ||||||||||||
Occurrence event ratea | 51 969 | 7.4b | 3.8 (3.6–3.9) | 16 745 | 6.7b | 0.8 (0.6–0.9) | 16 718 | 7.3b | 3.0 (2.8–3.3) | 18 506 | 8.3b | 7.2 (6.8–7.5) |
One or more event per hospitalizationc | 7019 | 100.0 | 20.1 (19.2–21.0) | 2507 | 35.7 | 4.9 (4.1–5.8) | 2279 | 32.5 | 19.8 (18.2–21.4) | 2233 | 31.8 | 37.4 (35.4–39.4) |
N/A indicates not applicable.
The numerator is the number of adverse events that occurred and the denominator is the number of adverse events for which patients were at risk.
Number of adverse events for which patients were at risk per hospitalization.
The numerator is the number of patients who experienced one or more adverse events and the denominator is the number of hospitalizations.