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. 2022 Nov 11;22:841. doi: 10.1186/s12879-022-07810-8

Table 2.

Epidemiology and outcomes of COBSI before and during SARS-CoV-2 periods by SARS-CoV-2 testing status

July 2019-February 2020 March 2020–September 4, 2021
Pre-pandemic period Pandemic period
Characteristics SARS-CoV-2 +  SARS-CoV-2 − SARS-CoV-2 not tested Total
20,113 1638 27,476 10,590 39,704
Unadjusted BSI rate per 1000 admissions 11.240 9.613c 15.818c 6.864c 11.508a
Mean age ± SD, (IQR; median) 65.1 ± 16.7 (55–78; 67) 66.2 ± 16.2 (56–79; 68)a 65.2 ± 16.3 (55–77; 67) 64.6 ± 16.6 (55–77; 67)a 65.2 ± 16.4 (55–77; 67)
Males, n (%) 10,467 (52.0) 843 (51.5) 14,751 (53.7)b 5560 (52.5) 21,154 (53.3%)a
Prior 30-day admission, (%) 13.2% (2655) 16.7% (274)c 14.4% (3945)c 14.9% (1581)c 14.6% (5800)c
Prior 90-day admission (%) 22.7% (4572) 27.2% (445)c 26.9% (7393)c 27.3% (2889)c 27.0% (10,727)c
 ≥1 Underlying conditionsd (%) 86.3% (17,356) 94.6% (1550)c 90.7% (24,932)c 83.9% (8889)c 89.1% (35,371)c
LOS (days): avg ± SD (IQR; median) 9.1 ± 8.3 (4–11; 7) 12.2 ± 11.8 (5–15; 9)c 9.2 ± 8.6 (4–11; 7) 8.3 ± 7.8 (4–10; 6)c 9.6 ± 8.6 (4–11; 7)
% Ventilatede (%) 4.7% (954) 10.7% (175)c 5.4% (1490)c 4.0% (424)a 5.3% (2089)b
ICU admission (%) 32.8% (6591) 36.6% (600)b 29.6% (8138)c 26.5% (2838)c 29.2% (11,576)c

Overall LOS (days):

avg ± SD (IQR; median)

12.1 ± 10.6 (6–15; 9) 15.5 ± 14.9 (6–20; 12)c 12.5 ± 11.7 (6–15, 9) 11.3 ± 10.7 (5–14; 8)c 12.3 ± 11.7 (5–15; 9)

ICU LOS (days):

avg ± SD (IQR; median)

4.7 ± 5.3 (2–6; 3) 6.5 ± 7.4 (2–8; 4)c 5.0 ± 6.8 (2–6; 3)a 4.6 ± 5.5 (1–6; 3)c 5 ± 6.6 (2–6; 3)b
Hospital mortality (%) NA 20.7% (237/1,146) 7.0% (1324/18,843) NA 7.8% (1567/20,064)

aP < .05; bP < .01; cP < .001 bivariate correlations compared to the pre-SARS-CoV-2 period

dIncludes the following baseline conditions occurring within the first 3 days of hospital admissions as determined by the maximum value of surrogate laboratory results: renal insufficiency (serum creatinine [SCr] > 2.0 mg/dL [to convert to micromoles per liter, multiply by 88.4]); kidney failure (blood urea nitrogen > 100 and SCr > 3.0 mg/dL); suspected sepsis (lactic acid > 2.0 or > 4.0 mmol/L); suspected heart failure (brain-type natriuretic peptide [BNP] > 400 pg/mL [to convert to nanograms per liter, multiply by 1.0] or N-terminal pro BNP > 900 pg/mL); myocardial inflammation (doubling of troponin drawn within 6 h final value: troponin 0.4 ng/L [to convert to micrograms per liter, multiply by 1.0], troponin T15 ng/L [to convert to micrograms per liter, multiply by 1.0] in male patients, troponin T10 ng/L in female patients, troponin I > 0.04 ng/mL [to convert to micrograms per liter, multiply by 1.0]); liver dysfunction (any of the following: alanine aminotransferase > 60 U/L [to convert to microkatals per liter, multiply by 0.0167], aspartate aminotransferase > 80 U/L [to convert to microkatals per liter, multiply by 0.0167], serum albumin < 3.0 g/dL [to convert to grams per liter, multiply by 10], international normalized ratio > 2.0 [and not currently receiving warfarin, rivaroxaban, apixaban, edoxaban, or betrixaban]); cytokine stimulation (any of the following: fibrinogen < 250 mg/dL [to convert to grams per liter, multiply by 0.01], C-reactive protein > 7.0 mg/dL [to convert to milligrams per liter, multiply by 10], D-dimer [dimerized plasmin fragment D] > 1000 ng/mL [to convert to nanomoles per liter, multiply by 5.476], erythrocyte sedimentation rate > 30 mm/h, or triglycerides > 265 mg/dL [to convert to millimoles per liter, multiply by 0.0113])

eThe patient was (a) started on intravenous (IV)/IV push (IVP) sedation medications (propofol, lorazepam, midazolam, dexmedetomidine, or ketamine) or IV/IVP opioids (fentanyl, remifentanil, sufentanil, or hydromorphone) with a duration ≥ 24 h and (b) ≥ 2 arterial blood gas results collected ≥ 24 h apart (on the first day of sedation medication and a subsequent result 24 h later)