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Review
. 2024 Sep 23;13(9):907.
doi: 10.3390/antibiotics13090907.

Comparing the Outcomes of Cefoperazone/Sulbactam-Based and Non-Cefoperazone/Sulbactam-Based Therapeutic Regimens in Patients with Multiresistant Acinetobacter baumannii Infections-A Meta-Analysis

Affiliations
Review

Comparing the Outcomes of Cefoperazone/Sulbactam-Based and Non-Cefoperazone/Sulbactam-Based Therapeutic Regimens in Patients with Multiresistant Acinetobacter baumannii Infections-A Meta-Analysis

Chienhsiu Huang et al. Antibiotics (Basel). .

Abstract

The addition of sulbactam restores the complete range of cefoperazone activity against bacteria and extends its spectrum of action to include the Acinetobacter species. The effectiveness of cefoperazone/sulbactam against multiresistant Acinetobacter baumannii has not been investigated. The purpose of the current meta-analysis was to compare the efficacy of cefoperazone/sulbactam-based therapeutic regimens and non-cefoperazone/sulbactam-based therapeutic regimens in the treatment of multiresistant Acinetobacter baumannii infections. The current meta-analysis of 10 retrospective studies provides evidence that cefoperazone/sulbactam-based therapeutic regimens are superior to non-cefoperazone/sulbactam-based therapeutic regimens in terms of 30-day mortality and clinical improvement in patients with multiresistant Acinetobacter baumannii infections. The risk of mortality was reduced by 38% among multiresistant Acinetobacter baumannii infections in patients who received cefoperazone/sulbactam-based therapeutic regimens. The cefoperazone/sulbactam-based combination therapy was superior to the cefoperazone/sulbactam monotherapy in terms of 30-day mortality when both therapeutic regimens were compared to the tigecycline monotherapy in patients with multiresistant Acinetobacter baumannii infections.

Keywords: Acinetobacter baumannii; cefoperazone; mortality; multiresistant; sulbactam.

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Conflict of interest statement

The authors declare no conflicts of interest.

Figures

Figure 1
Figure 1
Flow diagram of the study selection process.
Figure 2
Figure 2
The 30-day mortality rate between patients treated with cefoperazone/sulbactam-based therapeutic regimens and those treated with non-cefoperazone/sulbactam-based therapeutic regimens. (Inverted funnel plots revealed a symmetric relationship) [9,17,18,20,21,22].
Figure 3
Figure 3
The clinical improvement between patients treated with cefoperazone/sulbactam-based therapeutic regimens and those treated with non-cefoperazone/sulbactam-based therapeutic regimens. (Inverted funnel plots revealed a symmetric relationship) [14,15,16,19].
Figure 4
Figure 4
The 30-day mortality rate between patients treated with cefoperazone/sulbactam monotherapy and those treated with tigecycline monotherapy. (Inverted funnel plots revealed a symmetric relationship) [17,20,22].
Figure 4
Figure 4
The 30-day mortality rate between patients treated with cefoperazone/sulbactam monotherapy and those treated with tigecycline monotherapy. (Inverted funnel plots revealed a symmetric relationship) [17,20,22].
Figure 5
Figure 5
The 30-day mortality rate between patients treated with cefoperazone/sulbactam-based combination therapy and those treated with tigecycline monotherapy. (Inverted funnel plots revealed a symmetric relationship) [17,20,22].
Figure 5
Figure 5
The 30-day mortality rate between patients treated with cefoperazone/sulbactam-based combination therapy and those treated with tigecycline monotherapy. (Inverted funnel plots revealed a symmetric relationship) [17,20,22].

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