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首页> 外文期刊>The Pediatric infectious disease journal >Dynamics of pneumococcal nasopharyngeal carriage in children with nonresponsive acute otitis media treated with two regimens of intramuscular ceftriaxone.
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Dynamics of pneumococcal nasopharyngeal carriage in children with nonresponsive acute otitis media treated with two regimens of intramuscular ceftriaxone.

机译:用两种肌内头孢曲松治疗非反应性急性中耳炎儿童肺炎球菌鼻咽携带的动态。

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摘要

BACKGROUND: A 3-day intramuscular ceftriaxone regimen was superior to a 1-day regimen in the treatment of nonresponsive acute otitis media caused by resistant Streptococcus pneumoniae. However, the effect of various regimens of intramuscular cefriaxone on the nasopharyngeal carriage of S. pneumoniae and especially that of resistant strains during and after therapy has not been thoughtfully studied. OBJECTIVES: To compare the effect of one dose and three dose intramuscular ceftriaxone regimens on the nasopharyngeal carriage of S. pneumoniae in patients with nonresponsive acute otitis media treated with these two regimens and to document the dynamics of nasopharyngeal colonization with S. pneumoniae during and after completion of these two therapeutic regimens. PATIENTS AND METHODS: In a prospective study performed during January, 1998, through September, 1999, 170 evaluable patients ages 3 to 36 months with nonresponsive acute otitis media were randomized to receive the 1 (n = 83)- or 3 (n = 87)-day intramuscular ceftriaxone regimen (50 mg/kg/day), respectively. Nasopharyngeal cultures for S. pneumoniae were obtained on Days 1, 4 to 5, 11 to 14 and 28 to 30. Susceptibility of S. pneumoniae to penicillin and ceftriaxone was determined by E-test. RESULTS: On Day 1 nasopharyngeal S. pneumoniae carriage was found in 108 (64%) patients, 54 in each treatment group. Forty-seven of 54 (87%) and 9 of 54 (17%) S. pneumoniae isolates from the one dose group were nonsusceptible to penicillin and ceftriaxone, respectively; the respective values in the three dose group were 49 of 54 (91%) and 8 of 54 (15%). On Days 4 and 5 negative nasopharyngeal cultures were achieved in 43 of 83 (52%) and 70 of 87 (80%) cases from the one dose and three dose group, respectively (P < 0.001). Eradication of penicillin-nonsusceptible S. pneumoniae was achieved on Day 4 to 5 in 18 of 49 (37%) and 39 of 49 (80%) organisms isolated from the one dose and three dose groups, respectively (P < 0.001). Nasopharyngeal S. pneumoniae carriage among evaluable patients on Days 11 to 14 and Days 28 to 30 was 43 of 69 (62%) and 31 of 45 (69%) for the one dose group and 42 of 73 (58%) and 31 of 50 (62%) for the three dose group, respectively (P not significant). A decrease was observed during the study period in the proportion of highly penicillin-resistant S. pneumoniae isolated in the three dose group compared with the one dose group (30, 24, 17 and 13% vs. 30, 27, 19 and 26% at Days 1, 4 to 5, 11 to 14 and 28 to 30, respectively; P = 0.05). CONCLUSIONS: A marked reduction in the carriage of penicillin-nonsusceptible S. pneumoniae (including highly penicillin-resistant organisms) was achieved on Days 4 to 5 of therapy with both ceftriaxone regimens. The 3-day intramuscular ceftriaxone regimen was significantly superior to the 1-day regimen in the reduction of carriage during the treatment period. The reduction of overall S. pneumoniae nasopharyngeal carriage by both ceftriaxone regimens was a short-lived phenomenon followed by rapid recolonization ofthe nasopharynx.
机译:背景:3天的肌肉内头孢曲松方案优于一个抗性链球菌肺炎群的非反应性急性中耳炎的1天治疗方案。然而,肌肉内头孢酮肌瘤各种方案对肺炎肺炎鼻咽携带的影响,尚未仔细研究治疗期间和治疗后抗性菌株。目标:将一剂和三种剂量肌动肌肌细胞膜肿瘤患者对患有这两种方案治疗的非偏移急性中耳炎患者的鼻咽携带的鼻咽携带的效果,并记录在肺炎期间和后的肺炎患者的动态完成这两个治疗方案。患者和方法:在1998年1月的一项前瞻性研究中,通过1999年9月,170名可评价患者3至36个月的非偏移急性中耳炎患者被随机化接受1(n = 83) - 或3(n = 87 ) - 日肌肉肌肉内Xone方案(50 mg / kg /天)。在第1,4-5,11至14和28至30天获得肺炎肺炎的鼻咽培养物。通过电子试验确定S.肺炎肺炎肺蛋白和头孢噻嗪的易感性。结果:第1天鼻咽癌肺炎肺炎患者在108例(64%)患者中,每次治疗组54名。来自一剂组的40例54(87%)和9个(17%)的肺炎群岛分离物分别是青霉素和头孢菌素的Nonscrecte;三种剂量组的各自值为49,共54(91%)和8%(15%)。在第4天和第5天,分别在83(52%)和87个(80%)的40例中,分别从一剂和三剂量组中的43个(p <0.001)中实现了430例,50%的阴性鼻咽培养物。在49(37%)和39个(80%)生物中分别的第49(37%)和39个(80%)的49(80%)生物中分别的第49名(37%)和三剂量组中分别的第49名(P <0.001)中分离的第49名(37%)和39个(80%)和39名(P <0.001)中,达到了青霉素 - 非肌肉肺炎肺炎。 NoSopharyngeal S.在110至14天和第28至30天的可评估患者中的肺炎担荷载于69例(62%)和31个中的43个(69%),其中40例,42例为73(58%)和31个三种剂量组的50(62%)分别(P不显着)。在三种剂量组中分离出高度青霉素抗性S.肺炎的比例的研究期间观察到减少。与一剂组(30,24,17和13%对30,27,19和26%相比在第1,4至5,11至14和28至30天,分别在第1,4至5,11至14至30天。p = 0.05)。结论:在用Ceftriaxone方案的第4至5天疗法实现了青霉素 - 非肌肉肺炎肺炎肺炎肺炎(包括高度青霉素抗性生物)的显着减少。为期3天的肌肉内肌肉肿大方案明显优于治疗期间载体的1天方案。 Ceftriaxone方案的总体S.肺炎鼻咽携带的减少是一种短暂的现象,然后快速调整鼻咽。

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