新生儿凝固酶阴性葡萄球菌菌血症持续输注万古霉素与间歇输注万古霉素的比较:倾向匹配队列研究》。

Rémy Gérard,Emilie Pauquet,Barbara Ros,Philippe Lehours,Laurent Renesme
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摘要

背景凝固酶阴性葡萄球菌(CONS)是晚发新生儿败血症的主要病因,尤其是在早产儿中,其发病率和死亡率都很高。虽然万古霉素是治疗这些感染的一线药物,但新生儿的最佳用药仍不确定。目的我们旨在比较新生儿 CONS 菌血症患者接受调整后持续输注(CIV)与标准间歇输注(IIV)万古霉素治疗的结果。方法这项回顾性研究纳入了 110 名新生儿,经过倾向评分匹配后,CIV 组 29 人,IIV 组 47 人。结果匹配后,与 IIV 组相比,CIV 组的治疗失败率明显降低 [5/29 (17%) vs. 26/47 (44%); P = 0.014],24 小时后万古霉素达到治疗水平的比率更高 [20/29 (69%) vs. 26/47 (44%); P = 0.002]。结论与标准间歇输注相比,调整后的万古霉素持续输注在新生儿CONS菌血症中的治疗失败率较低,且不会增加肾毒性。然而,由于该研究采用的是观察性设计,因此需要更大规模的前瞻性研究来验证这些结果。
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Continuous Versus Intermittent Vancomycin Infusions for Coagulase-negative Staphylococcus Bacteremia in Neonates: A Propensity-matched Cohort Study.
BACKGROUND Coagulase-negative staphylococci (CONS) are a major cause of late-onset neonatal sepsis, particularly in preterm infants, with high morbidity and mortality. While vancomycin is the first-line treatment for these infections, the optimal administration in neonates remains uncertain. OBJECTIVE We aim to compare the outcomes of neonates with CONS bacteremia treated with adjusted continuous infusion (CIV) versus standard intermittent infusion (IIV) of vancomycin. METHODS This retrospective study included 110 neonates, with 29 in the CIV group and 47 in the IIV group after propensity score matching. The primary outcome was treatment failure defined by the persistence of a positive blood culture for the same organism after at least 48 hours of vancomycin treatment. RESULTS After matching, the CIV group exhibited significantly lower treatment failure rates [5/29 (17%) vs. 26/47 (44%); P = 0.014] and a higher rate of achieving therapeutic vancomycin levels after 24 hours [20/29 (69%) vs. 26/47 (44%); P = 0.002] compared to the IIV group. No significant differences were observed in terms of acute kidney failure between the 2 groups. CONCLUSION Adjusted continuous vancomycin infusion in neonates with CONS bacteremia is associated with a lower treatment failure rate without an increase in renal toxicity compared to standard intermittent infusion. However, due to the observational design, larger prospective studies are needed to validate these results.
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