Table 1.

Baseline Demographics and Vancomycin Treatment Characteristics

CharacteristicTrough-Guided (n = 150)AUC-Guided (n = 150)P Value
Age, y, mean ± SD53 ± 1655 ± 15.400
Race
 White88 (58.7)95 (63.3).407
 African American53 (35.3)48 (32.0).541
 Hispanic4 (2.7)2 (1.3).684
 Other5 (3.3)5 (3.3)1.0
Male sex99 (66.0)88 (58.7).190
Weight, kg, mean ± SD88.1 ± 25.886.2 ± 28.7.544
BMI, kg/m2, mean ± SD28.3 ± 7.528.5 ± 9.1.852
Baseline eGFR, mL/min
  >60120 (80.0)111 (74.0).217
 50–6011 (7.3)24 (16.0).019
 40–496 (4.0)8 (5.3).584
 30–3913 (8.7)7 (4.7).165
Chronic kidney disease5 (3.3)13 (8.7).052
Diabetes mellitus47 (31.3)40 (26.7).373
Cardiovascular disease56 (37.3)58 (38.7).812
Cirrhosis5 (3.3)7 (4.7).556
IV drug use11 (7.3)14 (9.3).531
Immunocompromised22 (14.7)21 (14.0).869
Pitt bacteremia score, mean ± SD0.59 ± 0.860.67 ± 0.97.451
ICU level of care at vancomycin initiation53 (35.3)42 (28.0).172
Mechanical ventilation at treatment initiation24 (16.0)18 (12.0).318
Vasopressor support at treatment initiation9 (6.0)9 (6.0)1.0
Concurrent antimicrobials at treatment initiation139 (92.7)133 (88.7).234
Infectious diseases consult117 (78.0)110 (73.3).346
Concurrent nephrotoxinsa115 (76.7)106 (70.7).238
Bacteremia98 (65.3)97 (64.7).904
Source control indicated but not achieved14 (9.3)14 (9.3)1.0
Clinical diagnosis.131
 Endocarditis4 (2.7)12 (8.0)
 Osteomyelitis or prosthetic joint infection31 (20.7)19 (12.7)
 Skin and soft tissue25 (16.7)26 (17.3)
 Line-associated infection13 (8.7)8 (5.3)
 Unknown33 (22.0)36 (24.0)
 Otherb44 (29.3)49 (32.7)
Organism.170
Staphylococcus aureus66 (44.0)62 (41.3)
  Methicillin susceptible15 (10.0)9 (6.0)
  Methicillin resistant51 (34.0)53 (35.3)
 Coagulase-negative staphylococci41 (27.3)52 (34.7)
Enterococcus faecalis7 (4.7)6 (4.0)
 Streptococcus spp5 (3.3)11 (7.3)
 Polymicrobial including S aureus11 (7.3)10 (6.7)
 Polymicrobial not including S aureus17 (11.3)6 (4)
 Other3 (2.0)3 (2.0)
Inpatient vancomycin treatment duration, d, mean ± SD9.6 ± 8.08.5 ± 5.6.164
Receipt of loading dose13 (8.7)14 (9.3).840
Loading dose, mg/kg, mean ± SD24.6 ± 2.825.3 ± 2.7.525
Total daily dose of initial regimen, mg/kg, mean ± SD26.6 ± 11.021.7 ± 7.8<.001
Vancomycin concentrations obtained per course, mean ± SD3.6 ± 2.64.5 ± 2.4.003
 Time to initial vancomycin concentration, h, mean ± SD44.8 ± 22.323.8 ± 14.1<.001
 Obtained within 72 h of first dose, mean ± SD1.4 ± 0.81.9 ± 0.8<.001
 Added to another blood draw, mean ± SD0.7 ± 0.91.7 ± 1.7<.001
CharacteristicTrough-Guided (n = 150)AUC-Guided (n = 150)P Value
Age, y, mean ± SD53 ± 1655 ± 15.400
Race
 White88 (58.7)95 (63.3).407
 African American53 (35.3)48 (32.0).541
 Hispanic4 (2.7)2 (1.3).684
 Other5 (3.3)5 (3.3)1.0
Male sex99 (66.0)88 (58.7).190
Weight, kg, mean ± SD88.1 ± 25.886.2 ± 28.7.544
BMI, kg/m2, mean ± SD28.3 ± 7.528.5 ± 9.1.852
Baseline eGFR, mL/min
  >60120 (80.0)111 (74.0).217
 50–6011 (7.3)24 (16.0).019
 40–496 (4.0)8 (5.3).584
 30–3913 (8.7)7 (4.7).165
Chronic kidney disease5 (3.3)13 (8.7).052
Diabetes mellitus47 (31.3)40 (26.7).373
Cardiovascular disease56 (37.3)58 (38.7).812
Cirrhosis5 (3.3)7 (4.7).556
IV drug use11 (7.3)14 (9.3).531
Immunocompromised22 (14.7)21 (14.0).869
Pitt bacteremia score, mean ± SD0.59 ± 0.860.67 ± 0.97.451
ICU level of care at vancomycin initiation53 (35.3)42 (28.0).172
Mechanical ventilation at treatment initiation24 (16.0)18 (12.0).318
Vasopressor support at treatment initiation9 (6.0)9 (6.0)1.0
Concurrent antimicrobials at treatment initiation139 (92.7)133 (88.7).234
Infectious diseases consult117 (78.0)110 (73.3).346
Concurrent nephrotoxinsa115 (76.7)106 (70.7).238
Bacteremia98 (65.3)97 (64.7).904
Source control indicated but not achieved14 (9.3)14 (9.3)1.0
Clinical diagnosis.131
 Endocarditis4 (2.7)12 (8.0)
 Osteomyelitis or prosthetic joint infection31 (20.7)19 (12.7)
 Skin and soft tissue25 (16.7)26 (17.3)
 Line-associated infection13 (8.7)8 (5.3)
 Unknown33 (22.0)36 (24.0)
 Otherb44 (29.3)49 (32.7)
Organism.170
Staphylococcus aureus66 (44.0)62 (41.3)
  Methicillin susceptible15 (10.0)9 (6.0)
  Methicillin resistant51 (34.0)53 (35.3)
 Coagulase-negative staphylococci41 (27.3)52 (34.7)
Enterococcus faecalis7 (4.7)6 (4.0)
 Streptococcus spp5 (3.3)11 (7.3)
 Polymicrobial including S aureus11 (7.3)10 (6.7)
 Polymicrobial not including S aureus17 (11.3)6 (4)
 Other3 (2.0)3 (2.0)
Inpatient vancomycin treatment duration, d, mean ± SD9.6 ± 8.08.5 ± 5.6.164
Receipt of loading dose13 (8.7)14 (9.3).840
Loading dose, mg/kg, mean ± SD24.6 ± 2.825.3 ± 2.7.525
Total daily dose of initial regimen, mg/kg, mean ± SD26.6 ± 11.021.7 ± 7.8<.001
Vancomycin concentrations obtained per course, mean ± SD3.6 ± 2.64.5 ± 2.4.003
 Time to initial vancomycin concentration, h, mean ± SD44.8 ± 22.323.8 ± 14.1<.001
 Obtained within 72 h of first dose, mean ± SD1.4 ± 0.81.9 ± 0.8<.001
 Added to another blood draw, mean ± SD0.7 ± 0.91.7 ± 1.7<.001

Data are presented as No. (%) unless otherwise indicated.

Abbreviations: AUC, area under the curve; BMI, body mass index; eGFR, estimated glomerular filtration rate; ICU, intensive care unit; IV, intravenous; SD, standard deviation.

aNephrotoxic agents: aminoglycosides, amphotericin B, angiotensin-converting enzyme inhibitors, angiotensin receptor blockers, cidofovir, cisplatin, contrast dye, IV cyclosporine, ganciclovir, interferon-α, lithium, loop diuretics, methotrexate, nonsteroidal anti-inflammatory agents, pentamidine, piperacillin-tazobactam, phenytoin, tenofovir disoproxil fumarate, thiazide diuretics, trimethoprim-sulfamethoxazole, tacrolimus.

bOther infection types included pneumonia (trough-guided: n = 7; AUC-guided: n = 10), septic arthritis (trough-guided: n = 5; AUC-guided: n = 4), meningitis (trough-guided: n = 1; AUC-guided: n = 0), urinary tract infections (trough-guided: n = 3; AUC-guided: n = 6), intra-abdominal infections (trough-guided: n = 7; AUC-guided: n = 3), and surgical site infections (trough-guided: n = 10; AUC-guided: n = 8).

Table 1.

Baseline Demographics and Vancomycin Treatment Characteristics

CharacteristicTrough-Guided (n = 150)AUC-Guided (n = 150)P Value
Age, y, mean ± SD53 ± 1655 ± 15.400
Race
 White88 (58.7)95 (63.3).407
 African American53 (35.3)48 (32.0).541
 Hispanic4 (2.7)2 (1.3).684
 Other5 (3.3)5 (3.3)1.0
Male sex99 (66.0)88 (58.7).190
Weight, kg, mean ± SD88.1 ± 25.886.2 ± 28.7.544
BMI, kg/m2, mean ± SD28.3 ± 7.528.5 ± 9.1.852
Baseline eGFR, mL/min
  >60120 (80.0)111 (74.0).217
 50–6011 (7.3)24 (16.0).019
 40–496 (4.0)8 (5.3).584
 30–3913 (8.7)7 (4.7).165
Chronic kidney disease5 (3.3)13 (8.7).052
Diabetes mellitus47 (31.3)40 (26.7).373
Cardiovascular disease56 (37.3)58 (38.7).812
Cirrhosis5 (3.3)7 (4.7).556
IV drug use11 (7.3)14 (9.3).531
Immunocompromised22 (14.7)21 (14.0).869
Pitt bacteremia score, mean ± SD0.59 ± 0.860.67 ± 0.97.451
ICU level of care at vancomycin initiation53 (35.3)42 (28.0).172
Mechanical ventilation at treatment initiation24 (16.0)18 (12.0).318
Vasopressor support at treatment initiation9 (6.0)9 (6.0)1.0
Concurrent antimicrobials at treatment initiation139 (92.7)133 (88.7).234
Infectious diseases consult117 (78.0)110 (73.3).346
Concurrent nephrotoxinsa115 (76.7)106 (70.7).238
Bacteremia98 (65.3)97 (64.7).904
Source control indicated but not achieved14 (9.3)14 (9.3)1.0
Clinical diagnosis.131
 Endocarditis4 (2.7)12 (8.0)
 Osteomyelitis or prosthetic joint infection31 (20.7)19 (12.7)
 Skin and soft tissue25 (16.7)26 (17.3)
 Line-associated infection13 (8.7)8 (5.3)
 Unknown33 (22.0)36 (24.0)
 Otherb44 (29.3)49 (32.7)
Organism.170
Staphylococcus aureus66 (44.0)62 (41.3)
  Methicillin susceptible15 (10.0)9 (6.0)
  Methicillin resistant51 (34.0)53 (35.3)
 Coagulase-negative staphylococci41 (27.3)52 (34.7)
Enterococcus faecalis7 (4.7)6 (4.0)
 Streptococcus spp5 (3.3)11 (7.3)
 Polymicrobial including S aureus11 (7.3)10 (6.7)
 Polymicrobial not including S aureus17 (11.3)6 (4)
 Other3 (2.0)3 (2.0)
Inpatient vancomycin treatment duration, d, mean ± SD9.6 ± 8.08.5 ± 5.6.164
Receipt of loading dose13 (8.7)14 (9.3).840
Loading dose, mg/kg, mean ± SD24.6 ± 2.825.3 ± 2.7.525
Total daily dose of initial regimen, mg/kg, mean ± SD26.6 ± 11.021.7 ± 7.8<.001
Vancomycin concentrations obtained per course, mean ± SD3.6 ± 2.64.5 ± 2.4.003
 Time to initial vancomycin concentration, h, mean ± SD44.8 ± 22.323.8 ± 14.1<.001
 Obtained within 72 h of first dose, mean ± SD1.4 ± 0.81.9 ± 0.8<.001
 Added to another blood draw, mean ± SD0.7 ± 0.91.7 ± 1.7<.001
CharacteristicTrough-Guided (n = 150)AUC-Guided (n = 150)P Value
Age, y, mean ± SD53 ± 1655 ± 15.400
Race
 White88 (58.7)95 (63.3).407
 African American53 (35.3)48 (32.0).541
 Hispanic4 (2.7)2 (1.3).684
 Other5 (3.3)5 (3.3)1.0
Male sex99 (66.0)88 (58.7).190
Weight, kg, mean ± SD88.1 ± 25.886.2 ± 28.7.544
BMI, kg/m2, mean ± SD28.3 ± 7.528.5 ± 9.1.852
Baseline eGFR, mL/min
  >60120 (80.0)111 (74.0).217
 50–6011 (7.3)24 (16.0).019
 40–496 (4.0)8 (5.3).584
 30–3913 (8.7)7 (4.7).165
Chronic kidney disease5 (3.3)13 (8.7).052
Diabetes mellitus47 (31.3)40 (26.7).373
Cardiovascular disease56 (37.3)58 (38.7).812
Cirrhosis5 (3.3)7 (4.7).556
IV drug use11 (7.3)14 (9.3).531
Immunocompromised22 (14.7)21 (14.0).869
Pitt bacteremia score, mean ± SD0.59 ± 0.860.67 ± 0.97.451
ICU level of care at vancomycin initiation53 (35.3)42 (28.0).172
Mechanical ventilation at treatment initiation24 (16.0)18 (12.0).318
Vasopressor support at treatment initiation9 (6.0)9 (6.0)1.0
Concurrent antimicrobials at treatment initiation139 (92.7)133 (88.7).234
Infectious diseases consult117 (78.0)110 (73.3).346
Concurrent nephrotoxinsa115 (76.7)106 (70.7).238
Bacteremia98 (65.3)97 (64.7).904
Source control indicated but not achieved14 (9.3)14 (9.3)1.0
Clinical diagnosis.131
 Endocarditis4 (2.7)12 (8.0)
 Osteomyelitis or prosthetic joint infection31 (20.7)19 (12.7)
 Skin and soft tissue25 (16.7)26 (17.3)
 Line-associated infection13 (8.7)8 (5.3)
 Unknown33 (22.0)36 (24.0)
 Otherb44 (29.3)49 (32.7)
Organism.170
Staphylococcus aureus66 (44.0)62 (41.3)
  Methicillin susceptible15 (10.0)9 (6.0)
  Methicillin resistant51 (34.0)53 (35.3)
 Coagulase-negative staphylococci41 (27.3)52 (34.7)
Enterococcus faecalis7 (4.7)6 (4.0)
 Streptococcus spp5 (3.3)11 (7.3)
 Polymicrobial including S aureus11 (7.3)10 (6.7)
 Polymicrobial not including S aureus17 (11.3)6 (4)
 Other3 (2.0)3 (2.0)
Inpatient vancomycin treatment duration, d, mean ± SD9.6 ± 8.08.5 ± 5.6.164
Receipt of loading dose13 (8.7)14 (9.3).840
Loading dose, mg/kg, mean ± SD24.6 ± 2.825.3 ± 2.7.525
Total daily dose of initial regimen, mg/kg, mean ± SD26.6 ± 11.021.7 ± 7.8<.001
Vancomycin concentrations obtained per course, mean ± SD3.6 ± 2.64.5 ± 2.4.003
 Time to initial vancomycin concentration, h, mean ± SD44.8 ± 22.323.8 ± 14.1<.001
 Obtained within 72 h of first dose, mean ± SD1.4 ± 0.81.9 ± 0.8<.001
 Added to another blood draw, mean ± SD0.7 ± 0.91.7 ± 1.7<.001

Data are presented as No. (%) unless otherwise indicated.

Abbreviations: AUC, area under the curve; BMI, body mass index; eGFR, estimated glomerular filtration rate; ICU, intensive care unit; IV, intravenous; SD, standard deviation.

aNephrotoxic agents: aminoglycosides, amphotericin B, angiotensin-converting enzyme inhibitors, angiotensin receptor blockers, cidofovir, cisplatin, contrast dye, IV cyclosporine, ganciclovir, interferon-α, lithium, loop diuretics, methotrexate, nonsteroidal anti-inflammatory agents, pentamidine, piperacillin-tazobactam, phenytoin, tenofovir disoproxil fumarate, thiazide diuretics, trimethoprim-sulfamethoxazole, tacrolimus.

bOther infection types included pneumonia (trough-guided: n = 7; AUC-guided: n = 10), septic arthritis (trough-guided: n = 5; AUC-guided: n = 4), meningitis (trough-guided: n = 1; AUC-guided: n = 0), urinary tract infections (trough-guided: n = 3; AUC-guided: n = 6), intra-abdominal infections (trough-guided: n = 7; AUC-guided: n = 3), and surgical site infections (trough-guided: n = 10; AUC-guided: n = 8).

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