Ceftaroline Efficacy and Safety in Treatment of Complicated Skin and Soft Tissue Infection: A Systemic Review and Meta-Analysis of Randomized Controlled Trials

被引:13
作者
Lan, Shao-Huan [1 ]
Chang, Shen-Peng [2 ]
Lai, Chih-Cheng [3 ]
Lu, Li-Chin [4 ]
Chao, Chien-Ming [3 ]
机构
[1] Putian Univ, Sch Pharmaceut Sci & Med Technol, Putian 351100, Peoples R China
[2] Chi Mei Med Ctr, Dept Pharm, Liouying 73657, Taiwan
[3] Chi Mei Med Ctr, Dept Intens Care Med, Liouying 73657, Taiwan
[4] Putian Univ, Sch Management, Putian 351100, Peoples R China
关键词
ceftaroline; complicated skin and skin structure infection; vancomycin; methicillin-resistant Staphylococcus aureus; RESISTANT STAPHYLOCOCCUS-AUREUS; COMMUNITY-ACQUIRED PNEUMONIA; IN-VITRO ACTIVITY; DOUBLE-BLIND; PHASE-III; COMPARATOR AGENTS; NON-INFERIORITY; UNITED-STATES; FOSAMIL; CEPHALOSPORIN;
D O I
10.3390/jcm8060776
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This study aims to assess the clinical efficacy and safety of ceftaroline for the treatment of complicated skin and skin structure infections (cSSSIs) in adult patients through meta-analysis. PubMed, Embase, ClinicalTrials.gov, and Cochrane databases were searched up to April 2019. Only randomized controlled trials (RCTs) that evaluated ceftaroline and other comparators for treating cSSSIs in adult patients were included. The primary outcome was the clinical cure rate, whereas the secondary outcomes were clinical failure rate, microbiological eradication rate, relapse rate, and risk of an adverse event (AE). Five RCTs were included. Overall, ceftaroline had a clinical cure rate similar to comparators in the treatment of cSSSIs in the modified intent-to-treat population (risk ratio (RR), 1.00; 95% confidence interval (CI), 0.97-1.04; I-2 = 0%) and in the clinically evaluable population (RR, 1.00; 95% CI, 0.97-1.03; I-2 = 0%). In addition, no significant difference was observed between ceftaroline and comparators for the treatment of infection with Staphylococcus aureus (RR, 1.01; 95% CI, 0.98-1.05; I-2 = 0%), methicillin-resistant S. aureus (RR, 0.99; 95% CI, 0.94-1.05; I-2 = 0%), methicillin-susceptible S. aureus (RR, 1.01; 95% CI, 0.96-1.06; I-2 = 26%), Streptococcus spp. (RR, 1.07; 95% CI, 0.92-1.24; I-2 = 73%), and Gram-negative bacteria (RR, 0.94; 95% CI, 0.83-1.08; I-2 = 0%). Furthermore, ceftaroline had a similar rate of microbiological eradication (92.2% vs. 92.6%, RR, 1.00; 95% CI, 0.97-1.03; I-2 = 9%) and relapse (6.9% vs. 9.1%, RR, 0.48; 95% CI, 0.14-1.74; I-2 = 0%) as comparators. Finally, the risks of treatment-emergent AEs (RR, 0.96; 95% CI, 0.88-1.05; I-2 = 0%), serious AEs (RR, 1.03; 95% CI, 0.63-1.68; I-2 = 0%), and discontinuation of study drug due to an AE (RR, 0.86; 95% CI, 0.50-1.49; I-2 = 34%) did not differ significantly between ceftaroline and comparators. In conclusion, the clinical efficacy of ceftaroline is as high as that of comparators in the treatment of cSSSIs in adult patients, and this antibiotic is well tolerated like the comparators.
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页数:10
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