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. 2021 May 23;8(7):ofab261. doi: 10.1093/ofid/ofab261

Table 3.

Bivariate Comparison of Baseline Demographics and Clinical Criteria Between Patients With 30-Day Mortality and Patients With No 30-Day Mortality

Criteria 30-Day Mortality (n = 101) No 30-Day Mortality (n = 712) P Value
Demographics
Age, y 71 (62–80) 59 (46–68) .006
Age ≥65 y 71 (70.3) 224 (31.5) <.001
Race .365
African American 78 (78.0) 535 (75.7) .610
Caucasian 19 (19.0) 137 (19.4) .929
Others 4 (3.9) 40 (5.6)
BMI ≥30 30 (30.0) 243 (34.2) .408
Comorbid conditions
AKI 41 (40.6) 175 (24.6) .001
Cerebrovascular diseasea 18 (17.8) 107 (15.0) .466
Chronic pulmonary diseaseb 36 (35.6) 176 (24.7) .019
Chronic kidney disease
Moderate to severe chronic kidney disease or on chronic dialysis 44 (43.6) 218 (30.6) .009
Chronic dialysisc 18 (17.8) 170 (23.9) .177
Connective tissue diseased 14 (13.9) 61 (8.6) .085
Dementia 18 (17.8) 55 (7.7) .001
Diabetes disease, any 35 (34.7) 291 (40.9) .233
Without end organ damage 5 (5.0) 82 (11.5) .046
With end organ damage 30 (29.7) 210 (29.5) .966
Heart failure 35 (34.7) 151 (21.2) .003
Hemiplegia 3 (3.0) 13 (1.8) .438
Immunodeficiency, any 9 (8.9) 37 (5.2) .131
AIDS (CD4 <200) 2 (2.0) 16 (2.2) .864
HIV 2 (2.0) 31 (4.4) .258
Leukemia 0 (0) 2 (0.3) .594
Lymphoma 2 (2.0) 7 (1.0) .370
Tumor, any 13 (12.9) 28 (3.9) <.001
Without metastasis 4 (4.0) 10 (1.4) .065
With metastasis 9 (8.9) 18 (2.5) .001
Liver disease, any 10 (9.9) 84 (11.8) .577
Milde 7 (6.9) 67 (9.4) .418
Moderate or severef 3 (3.0) 17 (2.4) .724
Myocardial infarction 16 (15.8) 46 (6.5) .001
No conditions 3 (3.0) 51 (7.2) .113
Peptic ulcer disease 2 (2.0) 5 (0.7) .193
Peripheral vascular diseaseg 19 (18.8) 116 (16.3) .524
Prior hospitalization for 48 h in 90 d before index culture 43 (42.6) 238 (33.4) .070
Prior MRSA in 365 d preceding index culture 9 (8.9) 76 (10.7) .588
Prior MSSA in 365 d preceding index culture 0 (0) 5 (0.7) .398
Prior surgery in 30 d preceding index culture 3 (3.0) 29 (4.1) .594
PWID 4 (4.0) 107 (15.0) .002
Sources of bacteremiah
Bone and joint 1 (1.0) 115 (16.2) <.001
Endovascular 1 (1.0) 3 (0.4) .445
Central nervous system abscess 0 (0.0) 8 (1.1) .284
Infective endocarditis 11 (10.9) 94 (13.2) .517
Intraabdominal 1 (1.0) 12 (1.7) .602
Intravenous catheter 9 (8.9) 125 (17.6) .028
Invasive prosthetic device 3 (3.0) 25 (3.5) .780
Other 6 (5.9) 75 (10.5) .149
Pneumonia 41 (40.6) 128 (18.0) <.001
Skin and soft tissue 12 (11.9) 189 (26.5) <.001
Urinary 5 (5.0) 21 (2.9) .285
Unknown 15 (14.9) 52 (7.3) .010
Vertebral abscess 1 (1.0) 8 (1.1) .904
Others factors
APACHE II 24 (18–31) 16 (10–22) <.001
APACHE ≥30 33 (33.0) 58 (8.2) <.001
CCI 4 (2–6) 3 (1–5) <.001
CCI ≥5 47 (46.5) 179 (25.1) <.001
Intensive care settingi 32 (32.3) 111 (15.7) <.001
Infectious Diseases consult 87 (86.1) 667 (93.7) .006
Source controlj 19 (19.6) 306 (44.7) <.001
Automated VAN MIC testing performed 98 (97.0) 689 (96.8) .889
0.5 8 (8.2) 39 (5.7) .328
1 62 (63.3) 481 (69.8) .190
2 28 (28.6) 169 (24.5) .387
VAN Etest performed 49 (48.5) 388 (54.5) .613
1 86 (22.2) 13 (26.5) .492
2 36 (73.5) 302 (77.8) .492
AKIk 21 (25.3) 31 (5.7) <.001
VAN TDM by AUCl 14 (17.7) 202 (39.6) <.001
VAN AUC 517.5 (358.5–555.4) 463.0 (380.0–543.4) .642
On at least 1 nephrotoxic agentm 18 (21.7) 77 (14.2) .077
On VAN 18 (21.7) 70 (12.9) .032
Not on VAN 5 (6.0) 45 (8.3) .476
Other safety outcome
CPK increasen 1 (1.0) 9 (1.3) .815
Clostridium difficile 7 (6.9) 18 (2.5) .016

Data are presented as median (IQR) and/or No. (%).

Abbreviations: AKI, acute kidney injury; APACHE II, Acute Physiology and Chronic Health Evaluation; BMI, body mass index; CCI, Carlson comorbidity index; CD4, cluster of differentiation 4; COPD, chronic obstructive pulmonary disease; CPK, creatinine phosphokinase; DVT, deep venous thrombosis; IQR, interquartile range; MRSA, methicillin-resistant Staphylococcus aureus; MSSA, methicillin-sensitive Staphylococcus aureus; OA, osteoarthritis; PWID, person who injects drugs; Scr, serum creatinine; TDM, therapeutic drug monitoring; TIA, transient ischemic attack; VAN, vancomycin.

aStroke or TIA.

bAsthma or COPD.

cHemodialysis or peritoneal dialysis.

dOA or rheumatic arthritis.

eChronic hepatitis without cirrhosis.

fPortal hypertension or cirrhosis.

gDVT, chronic venous disease.

hSome patients may have had more than 1 source of infection.

iWhen obtaining index culture.

jIn 30-day mortality, intravenous catheter removal (n = 3), incision and drainage (n = 1), debridement (n = 2). In patients with no 30-day mortality, intravenous catheter removal (n = 45), valvular replacement (n = 4), cardiac device removal (n = 7), incision and drainage (n = 36), debridement (n = 21), amputation (n = 3), other (n = 16).

kAmong patients who did not have hemodialysis or peritoneal dialysis (30-day mortality, n = 83, and no 30-day mortality, n = 542). AKI was defined as an increase in serum creatinine (Scr) of ≥0.5 mg/dL or a ≥50% increase of Scr from baseline, whichever is greater, on 2 consecutive measurements from initial VAN dose until 72 hours after the last dose [13, 35].

lAmong the entire population of patients managed with vancomycin for ≥48 hours (30-day mortality, n = 79, and no 30-day mortality, n = 510).

mMost common nephrotoxic agents among patients who were on VAN and in 30-day mortality group were diuretics (n = 11), followed by piperacillin-tazobactam and contrast media (n = 5, each). Among patients who were on VAN and were not in 30-day mortality group, most common were diuretics (n = 25), followed by piperacillin-tazobactam and contrast media (n = 5, each). Among patients who are not on VAN and experienced 30-day mortality group, most common were diuretics, non-steroidal anti-inflammatory drugs, and diuretics (n = 2, each). While among patients who are not on VAN and did not experience 30-day mortality, most were nephrotoxic agents are diuretics (n = 11), followed by angiotensin II converting enzyme inhibitor or angiotensin receptor blocker (n = 3).

nIncreased CPK was defined as increase of CPK to >600 U/L (if baseline <200 U/L) or >1000 U/L (if baseline >200 U/L) from initiation of drug to 72 hours after discontinuation of drug.