Response-Tailored or Standard-Duration Antibiotic Treatment for Infective Endocarditis

医学 感染性心内膜炎 心内膜炎 菌血症 抗生素 临床终点 外科 随机化 抗生素治疗 随机对照试验 置信区间 不利影响 内科学 临床试验 联合疗法 链球菌 预防性抗生素 意向治疗分析 重症监护医学 相对风险 药物治疗 心脏病 抗菌剂 血培养
作者
Henning Bundgaard,Mia Pries- Heje,Julie Hjulmand,Rasmus Hasselbalch,Peter Godsk Jørgensen,Søren Fanø,Nana Køber,Christian Tuxen,Nareen Kader,Ekim Seven,Lars Ege Rasmussen,Malene Wienberg,Niels Eske Bruun,Marlene Tofterup,Magnus Rasmussen,Lindsey R. Baden,Ann E. Woolley,Theis Lange,Jannik Helweg-Larsen,Jonas Agerlund Povlsen
出处
期刊:The New England Journal of Medicine [Massachusetts Medical Society]
标识
DOI:10.1056/nejmoa2607887
摘要

BACKGROUND: In patients with infective endocarditis on the left side of the heart, the current recommendation of up to 6 weeks of antibiotic therapy is based largely on expert consensus opinion. Whether a clinical response-tailored antibiotic management strategy can shorten treatment duration without compromising safety is unclear. METHODS: , or streptococcus species to receive either response-tailored or standard-duration antibiotic therapy. Before randomization, all the patients received at least the prespecified 2 to 4 weeks of therapy and met criteria for clinical stabilization. After randomization, patients in the tailored-therapy group discontinued antibiotics and those in the standard-therapy group continued standard treatment (total duration, 4 to 6 weeks). The primary efficacy end point was days alive without antibiotic treatment for infective endocarditis or bacteremia within 6 months after randomization (tested for superiority). The primary safety end point was a composite of death from any cause, unplanned cardiac surgery, or symptomatic embolic events within 6 months after randomization (tested for noninferiority; margin, 7.5 percentage points). Relapse of bacteremia or infective endocarditis was a key secondary end point. RESULTS: A total of 508 patients underwent randomization, with 255 assigned to response-tailored therapy and 253 to standard-duration therapy. The median time alive without antibiotic treatment was 183 days (interquartile range, 181 to 183) with tailored therapy and 169 days (interquartile range, 166 to 171) with standard therapy (Hodges-Lehmann estimated difference, 13 days; 95% confidence interval [CI], 12 to 13; P<0.001 for superiority). A primary safety end-point event occurred in 21 patients (8.2%) with tailored therapy and in 27 patients (10.7%) with standard therapy (absolute between-group difference, -2.4 percentage points; 95% CI, -7.7 to 2.7; P<0.001 for noninferiority), indicating noninferiority. Relapse occurred in 13 patients (5.1%) with tailored therapy and in 4 patients (1.6%) with standard therapy (P = 0.04). CONCLUSIONS: Among patients with infective endocarditis on the left side of the heart, the use of a response-tailored antibiotic strategy resulted in a longer time alive without antibiotic therapy than standard-duration therapy and met the criterion for noninferiority with respect to safety but was associated with a higher incidence of relapse of bacteremia or infective endocarditis. (Funded by Sygeforsikringen "danmark" and others; POET II ClinicalTrials.gov number, NCT03851575.).
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