Protocol update for the SABATO trial: a randomized controlled trial to assess early oral switch therapy in low-risk Staphylococcus aureus bloodstream infection

被引:6
|
作者
Kaasch, Achim J. [1 ,2 ]
Rommerskirchen, Anna [1 ]
Hellmich, Martin [3 ]
Faetkenheuer, Gerd [4 ,5 ]
Prinz-Langenohl, Reinhild [6 ]
Rieg, Siegbert [7 ]
Kern, Winfried, V [7 ]
Seifert, Harald [5 ,8 ]
机构
[1] Heinrich Heine Univ Dusseldorf, Inst Med Microbiol & Hosp Hyg, Fac Med, Dusseldorf, Germany
[2] Otto von Guericke Univ, Inst Med Microbiol & Hosp Hyg, Fac Med, Leipziger Str 44, D-39120 Magdeburg, Germany
[3] Univ Cologne, Fac Med, Inst Med Stat & Computat Biol, Cologne, Germany
[4] Univ Hosp Cologne, Dept Internal Med 1, Div Infect Dis, Cologne, Germany
[5] German Ctr Infect Res DZIF, Partner Site Bonn Cologne, Cologne, Germany
[6] Univ Cologne, Clin Trial Ctr Cologne, D-50935 Cologne, Germany
[7] Univ Freiburg, Med Ctr, Fac Med, Div Infect Dis,Dept Med 2, D-79106 Freiburg, Germany
[8] Univ Cologne, Inst Med Microbiol Immunol & Hyg, Cologne, Germany
关键词
Oral switch therapy; Intravenous; Antimicrobial; Bloodstream infection; Bacteremia; Staphylococcus aureus; Randomized controlled trial; Pragmatic trial;
D O I
10.1186/s13063-020-4102-0
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background SABATO (Staphylococcus aureus bacteremia antibiotic treatment options) is a randomized, parallel-group, clinical non-inferiority trial designed to examine the efficacy and safety of early oral switch therapy in low-risk Staphylococcus aureus infection. The original trial protocol was published in Trials (accessible at 10.1186/s13063-015-0973-x). Here we describe final amendments to the study protocol and discuss the underlying rationale. Methods/design Three major changes were introduced into the study protocol: (1) the inclusion and exclusion criteria were refined so that patients with certain comorbidities (end-stage renal disease, severe liver disease) and uninfected foreign bodies (orthopedic prosthesis, pacemaker, implanted cardiac cardioverter-defibrillator) became eligible for enrollment under certain conditions; (2) the target sample size was decreased by choosing a conventional non-inferiority margin of 10% and converting the interim analysis (215 patients) into the final analysis; and (3) an additional follow-up visit after 30 days was introduced to allow for a closer follow-up of patients. Conclusion Changes to the study protocol were introduced to improve the enrollment and follow-up of patients. Furthermore, the decrease of the sample size will facilitate completion of the trial.
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页数:3
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