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. 2024 Jun 25;79(5):1153–1161. doi: 10.1093/cid/ciae338

Table 1.

Characteristics of Included Patients

Characteristic Edinburgh Cohort
(n = 458)
ARREST Cohort
(n = 758)
SAFO Cohort
(n = 214)
P Value
Age, y 68 (52–79) 65 (50–76) 65 (54–75) .08
Sex, male 292 (53.2) NAa 150 (70.1) .11
Acquisition <.0001
 Community-acquired 181 (39.5) 485 (64.1) 78 (36.4)
 Healthcare-associated 110 (24.0) 140 (18.5) 52 (24.3)
 Nosocomial 167 (36.5) 132 (17.4) 84 (39.3)
Comorbidity
 Dementia 44 (9.6) 31 (4.1) 7 (3.3) .0002
 Chronic kidney disease 35 (7.6) 138 (18.3) 18 (8.4) <.0001
 Liver diseaseb 57 (12.4) 56 (7.4) 13 (6.1) .004
 Vascular diseasec 121 (26.4) NA 59 (27.6) .77
 Prosthetic cardiac materiald 46 (10.0) NA 16 (7.5) .31
 Injection drug use 41 (9.0) 83 (11.1) 0 <.0001
Vital signs
 Heart rate, beats per minute 98 (85–110) 94 (82–107) NA .005
 Temperature, °C 38.2 (37.6–38.8) 37.0 (37.0–38.0) 37.3 (36.5–38.3) <.0001
Laboratory measurements
 Hemoglobin, g/L 114 (100–129) 107 (93–122) NA <.0001
 Creatinine, µmol/L 90 (65–138) 80 (61–131) 80 (62–123) .05
 C-reactive protein, mg/L 156 (69–273) 150 (87–218) NA .15
Staphylococcus aureus bacteremia characteristics
 Methicillin-resistant S. aureus 17 (3.7) 47 (6.2) 0 <.0001
 Infective endocarditis 35 (7.6) 40 (5.3) 15 (7.0) .21
 Other metastatic focie 99 (21.6) 203 (26.8) 49 (22.9) .11
Source of bacteremia <.0001
 Unknown 163 (35.6) 221 (29.2) 70 (32.7)
 Intravenous catheter 93 (20.3) 141 (18.6) 68 (31.8)
 Skin or soft tissue infection 88 (19.2) 293 (38.7) 39 (18.2)
 Other 61 (13.3)f 55 (7.3)g 20 (9.3)
 Respiratory 28 (6.1) 29 (3.8) 4 (1.9)
 Urine 25 (5.5) 19 (2.5) 13 (6.1)
All-cause 84-day mortality 121 (26.4) 56/388 (14.4)h 17/110 (15.5)h <.0001

Continuous values are shown as median (interquartile range). Categorical variables are shown as count (%). Variables not available in the ARREST dataset are represented as NA. Vital signs and laboratory measurements were recorded at the time of the index blood culture in the Edinburgh and SAFO cohorts. In the ARREST trial, baseline laboratory measurements were those closest to randomization (preceding 4 days or 1 day post-randomization); for vital signs, the highest value within 24 hours of randomization was taken. Abbreviation: NA, not available.

aNot available due to participant deidentification.

bPeople with Child-Pugh C liver cirrhosis were excluded from the SAFO trial.

cPeripheral vascular disease, myocardial infarction, or stroke.

dImplanted cardiac devices, including pacemakers, implantable automatic cardioverter-defibrillator, and left ventricular assist devices, but not including prosthetic heart valves.

eVertebral osteomyelitis, epidural abscess, native joint septic arthritis, prosthetic joint infection, deep tissue abscess.

fInjection drug use and bone classified as “other.”

g“Other” sources not specified.

hData shown for trial control arms.