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Table 3 Treatment regimens and outcomes of various infections with carbapenemase-producing organisms reported in the literature

From: Treatment for infections with carbapenem-resistant Enterobacteriaceae: what options do we still have?

Infection

Pathogens

Number

Treatment

Mortality

Reference

Bacteremia

KPC

125

Monotherapy

25/46 (54%)

[23]

K. pneumoniae

Combination therapy

27/79 (34%)

7/23 (30%)

Colistina + tigecyclineb

6/12 (50%)

2/16 (12%)

Tigecycline + gentamicinc

Colistin + tigecycline + meropenemd

Bacteremia

KPC

41

Monotherapy

11/19 (58%)

[22]

K. pneumoniae

Combination therapye

2/15 (13%)

1/5 (20%)

Colistin + carbapenem

0/3 (0%)

0/2 (0%)

Tigecycline + carbapenem

Tigecycline + aminoglycoside

Trauma ICU

KPC

26

Combination therapy

2/26 (8%)

[33]

VAP

K. pneumoniae

Bacteremia

Tigecyclinef + gentamicing ± fosfomycinh

Tigecycline plus colistini ± fosfomycin

Bacteremia

Acinetobacter

28

Monotherapy (colistinj)

2/5 (40%)

[17]

VAP

Pseudomonas

Combination therapy

3/14 (21 %)

KPC K. pneumoniae

Colistin + aminoglycoside

Colistin plus carbapenem

ICU

KPC K. pneumoniae

11

Combination therapy

2/11 (18%)

[34]

VAP ± bacteremia

UTI, wound

Fosfomycink + colistin

Fosfomycin + gentamicin

Fosfomycin + piperacillin/tazobactam

ICU bacteremia

KPC K. pneumoniae

48

Combination therapy

18/48 (37.5%)

[35]

VAP

Pseudomonas

Fosfomycinl + colistin

Fosfomycin + tigecycline

UTI

KPC K. pneumoniae

21

Gentamicin

0/7 (0%)

[36]

Other

0/7 (0%)

Doxycycline

Ciprofloxacin

Nitrofurantoin

Colistin

UTI (including colonization)

CRE

136

Treatment receivedm

9/136 (7%)

[37]

Polymyxin B

Tigecycline

Aminoglycoside

   

No treatment

  
  1. aInitial loading dose, followed by 6 to 9 million IU/day; binitial loading dose followed by 100 to 200 mg/day; c4 to 5 mg/kg per day; d2 g every 8 hours infused over at least 3 hours; evarious other combinations used infrequently; the other patient who died on combination therapy received carbapenem-fluoroquinolone; f100 mg intravenous (IV) every 12 hours; g5 to 7 mg/kg per day; h4.5 million IU every 12 hours; i3 g IV every 8 hours; j9 million IU loading dose, followed by 4.5 million IU every 12 hours if normal renal function; k4 g IV every 6 hours; lIV dose up to 24 g/day; mrates of microbiological cure were 88% in the aminoglycoside group (n = 41), 64% in the polymyxin B group (n = 25), 43% in the tigecycline group (n = 21), and 36% in the no treatment group (n = 69). CRE, carbapenem-resistant Enterobacteriaceae; KPC, Klebsiella pneumoniae carbapenemase; UTI, urinary tract infection; VAP, ventilator-associated pneumonia.