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Partial oral antibiotic treatment for bacterial brain abscess: an open-label randomized non-inferiority trial (ORAL)
被引:9
作者:
Bodilsen, Jacob
[1
,2
]
Brouwer, Matthijs C.
[2
,3
]
van de Beek, Diederik
[2
,3
]
Tattevin, Pierre
[2
,4
,5
,6
]
Tong, Steven
[7
,8
]
Naucler, Pontus
[9
]
Nielsen, Henrik
[1
,2
,10
]
机构:
[1] Aalborg Univ Hosp, Dept Infect Dis, Mollepk Vej 4, DK-9000 Aalborg, Denmark
[2] European Soc Clin Microbiol & Infect Dis Study Gr, Basel, Switzerland
[3] Univ Amsterdam, Dept Neurol, Amsterdam UMC, Amsterdam Neurosci, Amsterdam, Netherlands
[4] Pontchaillou Univ Hosp, Dept Infect Dis, Rennes, France
[5] Pontchaillou Univ Hosp, Intens Care Unit, Rennes, France
[6] Reseau Natl Rech Clin Infectiol RENARCI, Paris, France
[7] Royal Melbourne Hosp, Victorian Infect Dis Serv, Parkville, Vic, Australia
[8] Univ Melbourne, Peter Doherty Inst Infect & Immun, Dept Infect Dis, Melbourne, Vic, Australia
[9] Karolinska Univ Hosp, Dept Infect Dis, Stockholm, Sweden
[10] Aalborg Univ Hosp, Dept Clin Med, Aalborg, Denmark
来源:
关键词:
Brain abscess;
Cerebral abscess;
Treatment;
Randomized controlled trial;
Non-inferiority;
Antibiotics;
Oral;
Intravenous;
MANAGEMENT;
RELIABILITY;
THERAPY;
D O I:
10.1186/s13063-021-05783-8
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: The advised standard treatment for bacterial brain abscess following surgery is 6 to 8 weeks of intravenous (IV) antibiotic treatment, but an early switch to oral antibiotic treatment has been suggested to be equally effective. Methods: This investigator-initiated, international, multi-center, parallel group, open-label, randomized (1:1 allocation) controlled trial will examine if oral treatment after 2 weeks of IV antibiotic therapy is non-inferior to standard 6-8 weeks of IV antibiotics for bacterial brain abscess in adults (>= 18 years of age). The study will be conducted at hospitals across Denmark, the Netherlands, France, Australia, and Sweden. Exclusion criteria are severe immunocompromise or impaired gastro-intestinal absorption, pregnancy, device-related brain abscesses, and brain abscess caused by nocardia, tuberculosis, or Pseudomonas spp. The primary objective is a composite endpoint at 6 months after randomization consisting of all-cause mortality, intraventricular rupture of brain abscess, unplanned re-aspiration or excision of brain abscess, relapse, or recurrence. The primary endpoint will be adjudicated by an independent blinded endpoint committee. Secondary outcomes include extended Glasgow Outcome Scale scores and all-cause mortality at end of treatment as well as 3, 6, and 12 months since randomization, completion of assigned treatment, IV catheter associated complications, durations of admission and antibiotic treatment, severe adverse events, quality of life scores, and cognitive evaluations. The planned sample size is 450 patients for a one-sided alpha of 0.025 and a power of 90% to exclude a difference in favor of standard treatment of more than 10%. Date of initiation of first study center was November 3, 2020, with active recruitment for 3 years and follow-up for 1 year of all patients. Discussion: The results of this study may guide future recommendations for treatment of bacterial brain abscess. If early transition to oral antibiotics proves non-inferior to standard IV treatment, this will provide considerable health and costs benefits.
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页数:17
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