Volume 25, Number 10—October 2019
Dispatch
Control and Elimination of Extensively Drug-Resistant Acinetobacter baumanii in an Intensive Care Unit
Table 1
Characteristics | Period 1† | Period 2‡ | p value |
|
---|---|---|---|---|
Patient data | ||||
No. patients | 213 | 324 | NA |
|
Sex | ||||
F | 79 | 144 | ||
M | 134 | 180 | ||
Mean age | 69 | 68 | ||
Mean length of hospital stay, d | 6.8 | 6 | ||
Days in ICU |
1,128 |
1,804 |
||
Type of admission | ||||
Medical | 163 | 253 | NA | |
Surgical | 50 | 71 | ||
Admitted from home or ED | 73 | 114 | ||
Transferred from ward | 79 | 141 | ||
Transferred from other hospital | 10 | 16 | ||
Postoperative |
51 |
57 |
||
Intubation | ||||
At admission | 64 | 85 | ||
After admission |
14 |
16 |
||
Outcome | ||||
A. baumanii VAP incidence, % | 15 | 3.7 | 0.007 | |
Discharged | 170 | 259 | ||
Deceased | 43 | 64 | ||
Total AB VAP events | 32 | 12 | ||
Deceased during VAP |
17 |
4 |
||
ICU mean mortality rate/month, % | 20.4 | 19.3 | 0.168 | |
AB VAP case fatality ratio, % |
7.9 |
1.2 |
0.006 |
|
No. XDR A. baumanii VAP courses received | ||||
Colistin and carbapenem | 17 | 2 | ||
Colistin and tigecycline | 6 | 2 | ||
Colistin monotherapy | 6 | 6 | ||
Tigecycline |
3 |
2 |
||
Carbapenem consumption, DDD§ | ||||
Group 1 | 333 | 320 | 0.465 | |
Group 2 | 455 | 224 | 0.042 | |
Group 3 | 541 | 223 | <0.005 | |
Group 4 | 165 | 145 | 0.808 | |
Group 5 | ||||
Colistin | 20 | 9 | <0.019 | |
Tigecycline |
84 |
62 |
0.570 |
|
Total restricted antimicrobial drugs, DDD | 1,265 | 663 | <0.005 |
*Bold indicates statistical significance. DDD, defined daily doses; ED, emergency department, ESBL, extended-spectrum β-lactamase; ICU, intensive care unit; NA, not applicable; VAP, ventilator-associated pneumonia; XDR, extensively drug-resistant.
†During February 1, 2016–June 30, 2016, ICU patients received colistin/carbapenem therapy for A. baumannii infections.
‡During July 1, 2016–January 31, 2017, ICU implemented carbapenem-sparing regimen for A. baumannii infections.
§Group 1, antimicrobial drugs that do not require infectious disease specialist preapproval, such as third-generation cephalosporins, amoxicillin/clavulanic acid, and quinolones; group 2, oral vancomycin and metronidazole used for Clostridioides difficile therapy; group 3, imipenem and meropenem; group 4, broad-spectrum carbapenem-sparing regimens, including piperacillin/tazobactam, cefepime, ceftazidime, amikacin; and group 5, the XDR A. baumanii–active antimicrobial drugs colistin and tigecycline.
1These authors contributed equally to this article.