金黄色葡萄球菌菌血症患儿改用口服抗生素的临床效果

IF 1.3 Q3 PEDIATRICS Turkish archives of pediatrics Pub Date : 2024-09-02 DOI:10.5152/TurkArchPediatr.2024.24108
Salih Demirhan, Brenda I Anosike
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引用次数: 0

摘要

金黄色葡萄球菌是导致儿童菌血症的主要原因之一。在这项研究中,我们旨在评估本中心在小儿金黄色葡萄球菌菌血症(SAB)的病因、管理和治疗效果方面的经验,尤其是在过渡到口服抗生素治疗方面。这项回顾性队列研究纳入了 5 年内诊断为 SAB 的 19 岁以下儿童。主要结果是与 SAB 相关的不良临床结局,即:(1)停止 SAB 治疗后 30 天内 SAB 复发;(2)发现 SAB 后 30 天内任何原因的死亡。在 5 年的时间里,共纳入了 76 名患者的 88 次 SAB 病例。最常见的 SAB 源头是中心管路感染(34 例),其次是骨关节感染(24 例)。所有患者都接受了至少一天的静脉注射抗生素治疗,45.5% 的 SAB 病例改用口服药物治疗。口服换药组的 SAB 来源为骨关节(21 例)、皮肤和软组织(7 例)、中心静脉(3 例)、血栓性静脉炎(2 例)、头颈部感染(1 例)和未知(6 例)。初始治疗结束后 30 天内死亡和 30 天内 SAB 复发的 SAB 例数分别为 3 例和 5 例。口服换药组患者中没有人出现不良临床结局。我们的研究结果表明,儿童 30 天内任何原因的死亡率和与 SAB 相关的死亡率都很低。与越来越多的成人文献相似,在选定的患者中,SAB 治疗中的口服转换与不良的 SAB 后果无关。
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Clinical Outcomes of Oral Antibiotic Switch in Children with Staphylococcus aureus Bacteremia.

Staphylococcus aureus is one of the leading causes of bacteremia in children. In this study, we aimed to evaluate our center's experience on the etiology, management, and outcomes of pediatric Staphylococcus aureus bacteremia (SAB) with particular focus on transitioning to oral antibiotic therapy. This retrospective cohort study included children aged ≤ 19 years diagnosed with SAB over a 5-year period. The main outcome was poor clinical outcome related to SAB defined as (1) recurrence of SAB within 30 days after discontinuation of SAB treatment and (2) any-cause mortality within 30 days after detection of SAB. Over a 5-year period, 88 SAB episodes of 76 unique patients were included. The most common source of SAB attributed to central line (n = 34), followed by osteoarticular (n = 24), infections. All patients received at least one day of intravenous (IV) antibiotics and treatment was switched to an oral agent in 45.5% of SAB episodes. Sources of SAB in the oral switch group were osteoarticular (n = 21), skin and soft tissue (n = 7), central line (n = 3), thrombophlebitis (n = 2), head and neck infection (n = 1), and unknown (n = 6). 30-day mortality and SAB recurrence within 30 days after initial treatment completion occurred in 3 and 5 SAB episodes, respectively. None of the patients in oral switch group had poor clinical outcomes. Our study results indicate that 30-day any-cause mortality and SAB-related mortality is low in children. Similar to growing adult literature, oral switch in SAB treatment was not associated with poor SAB outcomes in selected patients.

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