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Carbapenem-resistant Acinetobacter baumannii: Colonization, Infection and Current Treatment Options

Journal

INFECTIOUS DISEASES AND THERAPY
Volume 11, Issue 2, Pages 683-694

Publisher

SPRINGER LONDON LTD
DOI: 10.1007/s40121-022-00597-w

Keywords

Acinetobacter infections; Drug resistance; Multiple; Carbapenem-resistant enterobacteriaceae

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Carbapenem-resistant Acinetobacter baumannii (CRAB) predominantly causes colonization and infection in hospitalized patients. Distinguishing between the two is challenging. Treatment should be based on clear signs of infection and consideration of the presence of indwelling medical devices. Current treatment options are limited and combination therapy appears to be the best option.
Carbapenem-resistant Acinetobacter baumannii (CRAB) causes colonization and infection predominantly in hospitalized patients. Distinction between the two is a challenge. When CRAB is isolated from a non-sterile site (soft tissue, respiratory samples, etc.), it probably represents colonization unless clear signs of infection (fever, elevated white blood count, elevated inflammatory markers and abnormal imaging) are present. Treatment is warranted only for true infections. In normally sterile sites (blood, cerebrospinal fluid) the presence of indwelling medical devices (catheters, stents) should be considered when evaluating positive cultures. In the absence of such devices, the isolate represents an infection and should be treated. If an indwelling device is present and there are no signs of active infection, the device should be replaced if possible, and no treatment is required. If there are signs of an active infection the device should be removed or replaced, and treatment should be administered. Current treatments options and clinical data are limited. No agent or combination regimen has been shown to be superior to any other in randomized clinical trials. Ampicillin-sulbactam appears to have the best evidence for initial use. This is probably due to its ability to saturate penicillin-binding proteins 1 and 3 when given in high dose. Tigecycline when used should be given in high dose as well. Polymyxins are a treatment option but are difficult to dose correctly and have significant side effects. Newer treatment options such as eravacycline and cefiderocol have potential; however, currently there are not enough data to support their use as single agents. Combination therapy appears to be the best treatment option and should always include high-dose ampicillin-sulbactam combined with another active agent such as high-dose tigecycline, polymyxins, etc. These infections require a high complexity of skill, and an infectious disease specialist should be involved in the management of these patients.

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