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头孢克肟或阿莫西林克拉维酸治疗对急性中耳炎患儿肺炎链球菌和流感嗜血杆菌鼻咽部携带情况的影响。

Effects of cefixime or co-amoxiclav treatment on nasopharyngeal carriage of Streptococcus pneumoniae and Haemophilus influenzae in children with acute otitis media.

作者信息

Dabernat H, Geslin P, Megraud F, Bégué P, Boulesteix J, Dubreuil C, de La Roque F, Trinh A, Scheimberg A

机构信息

Laboratoire Central de Microbiologie, CHU, Hôpital Purpan, Toulouse, France.

出版信息

J Antimicrob Chemother. 1998 Feb;41(2):253-8. doi: 10.1093/jac/41.2.253.

Abstract

A multicentre, open-label, randomized study was performed in 501 out-patients with acute otitis media, aged 6-36 months, to study the impact of treatment with either cefixime suspension 8 mg/kg/day bd or co-amoxiclav suspension 80 mg/kg/day tds for 10 days on nasopharyngeal carriage of Streptococcus pneumoniae and Haemophilus influenzae. Of 426 patients with nasopharyngeal cultures at entry to the trial, end of treatment and at follow-up visit (35 days after inclusion), significant changes in carriage of S. pneumoniae were observed. The proportion of penicillin-resistant S. pneumoniae was higher in the samples taken at the end of treatment and follow-up than in those taken at inclusion, while the total number of children with this microorganism was lower. The difference at the end of treatment was greater with co-amoxiclav than with cefixime. For H. influenzae the resistance rate remained steady while the number of children with this microorganism decreased. At follow-up there was no significant difference between the two groups in terms of nasopharyngeal positive culture for S. pneumoniae or H. influenzae. Despite these differences, successful clinical responses were similar at the end of treatment and at follow-up.

摘要

一项多中心、开放标签、随机研究纳入了501名6至36个月大的急性中耳炎门诊患者,旨在研究10天内每日两次服用8mg/kg头孢克肟混悬液或每日三次服用80mg/kg阿莫西林克拉维酸钾混悬液对肺炎链球菌和流感嗜血杆菌鼻咽部携带情况的影响。在426名入组时、治疗结束时及随访(纳入后35天)进行鼻咽部培养的患者中,观察到肺炎链球菌携带情况有显著变化。治疗结束时和随访时采集的样本中,青霉素耐药肺炎链球菌的比例高于入组时,而携带该微生物的儿童总数较低。治疗结束时,阿莫西林克拉维酸钾组的差异比头孢克肟组更大。对于流感嗜血杆菌,耐药率保持稳定,而携带该微生物的儿童数量减少。随访时,两组在肺炎链球菌或流感嗜血杆菌鼻咽部阳性培养方面无显著差异。尽管存在这些差异,但治疗结束时和随访时的临床成功反应相似。

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