高风险环境下肺炎住院患儿延长抗生素疗程与标准疗程治疗 24 个月的结果:随机对照试验。

IF 2.9 4区 医学 Q3 IMMUNOLOGY Pediatric Infectious Disease Journal Pub Date : 2024-09-01 Epub Date: 2024-06-03 DOI:10.1097/INF.0000000000004407
Hing C Kok, Gabrielle B McCallum, Stephanie T Yerkovich, Keith Grimwood, Siew M Fong, Anna M Nathan, Catherine A Byrnes, Robert S Ware, Nachal Nachiappan, Noorazlina Saari, Peter S Morris, Tsin W Yeo, Victor M Oguoma, I Brent Masters, Jessie A de Bruyne, Kah P Eg, Bilawara Lee, Mong H Ooi, John W Upham, Paul J Torzillo, Anne B Chang
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引用次数: 0

摘要

背景:小儿社区获得性肺炎(CAP)可导致长期呼吸系统后遗症,包括支气管扩张。我们研究了延长抗生素疗程(13-14 天)与标准疗程(5-6 天)相比,是否能改善慢性呼吸道疾病高危人群中因 CAP 住院儿童的长期预后:我们在澳大利亚、新西兰和马来西亚的 7 家医院开展了一项多中心、双盲、优势随机对照试验。年龄在 3 个月至 5 岁以下的儿童因影像学确诊的 CAP 而住院,先接受 1-3 天的静脉抗生素治疗,然后口服 3 天的阿莫西林-克拉维酸钾,这些儿童被随机分配到延长疗程组(口服阿莫西林-克拉维酸钾 8 天)或标准疗程组(口服安慰剂 8 天)。在 12 个月和 24 个月时对儿童进行复查。主要结果是儿童出院后24个月时出现慢性呼吸道症状/体征(12个月和24个月时慢性咳嗽;24个月时急性下呼吸道感染住院次数≥1次;或12个月时出现持续性和/或新的胸部放射学体征)的复合终点,采用意向性治疗进行分析,其中随访不完全的儿童被假定为出现慢性呼吸道症状/体征("最坏情况"):共有 324 名儿童接受了随机治疗[延长疗程(163 人),标准疗程(161 人)]。就主要结果而言,在扩展课程和标准课程中,分别有 97/163 名(60%)和 94/161 名(58%)儿童出现慢性呼吸道症状/体征[相对风险 (RR) = 1.02,95% 置信区间 (CI):0.85-1.22]。在已知所有子综合结果的儿童中,组间慢性呼吸道症状/体征的相对风险(RR)= 1.10,95% 置信区间(CI):0.69-1.76 [扩展课程=27/93(29%),标准课程=24/91(26%)]。其他敏感性分析也显示组间无差异:结论:在因 CAP 住院的高危人群中,使用 13-14 天抗生素(与 5-6 天)并不能改善长期呼吸系统预后。
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Twenty-four Month Outcomes of Extended- Versus Standard-course Antibiotic Therapy in Children Hospitalized With Pneumonia in High-risk Settings: A Randomized Controlled Trial.

Background: Pediatric community-acquired pneumonia (CAP) can lead to long-term respiratory sequelae, including bronchiectasis. We determined if an extended (13-14 days) versus standard (5-6 days) antibiotic course improves long-term outcomes in children hospitalized with CAP from populations at high risk of chronic respiratory disease.

Methods: We undertook a multicenter, double-blind, superiority, randomized controlled trial involving 7 Australian, New Zealand, and Malaysian hospitals. Children aged 3 months to ≤5 years hospitalized with radiographic-confirmed CAP who received 1-3 days of intravenous antibiotics, then 3 days of oral amoxicillin-clavulanate, were randomized to either extended-course (8-day oral amoxicillin-clavulanate) or standard-course (8-day oral placebo) arms. Children were reviewed at 12 and 24 months. The primary outcome was children with the composite endpoint of chronic respiratory symptoms/signs (chronic cough at 12 and 24 months; ≥1 subsequent hospitalized acute lower respiratory infection by 24 months; or persistent and/or new chest radiographic signs at 12-months) at 24-months postdischarge, analyzed by intention-to-treat, where children with incomplete follow-up were assumed to have chronic respiratory symptoms/signs ("worst-case" scenario).

Results: A total of 324 children were randomized [extended-course (n = 163), standard-course (n = 161)]. For our primary outcome, chronic respiratory symptoms/signs occurred in 97/163 (60%) and 94/161 (58%) children in the extended-courses and standard-courses, respectively [relative risk (RR) = 1.02, 95% confidence interval (CI): 0.85-1.22]. Among children where all sub-composite outcomes were known, chronic respiratory symptoms/signs between groups, RR = 1.10, 95% CI: 0.69-1.76 [extended-course = 27/93 (29%) and standard-course = 24/91 (26%)]. Additional sensitivity analyses also revealed no between-group differences.

Conclusion: Among children from high-risk populations hospitalized with CAP, 13-14 days of antibiotics (versus 5-6 days), did not improve long-term respiratory outcomes.

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来源期刊
CiteScore
6.30
自引率
2.80%
发文量
566
审稿时长
2-4 weeks
期刊介绍: ​​The Pediatric Infectious Disease Journal® (PIDJ) is a complete, up-to-the-minute resource on infectious diseases in children. Through a mix of original studies, informative review articles, and unique case reports, PIDJ delivers the latest insights on combating disease in children — from state-of-the-art diagnostic techniques to the most effective drug therapies and other treatment protocols. It is a resource that can improve patient care and stimulate your personal research.
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