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Prevention of Pneumococcal Disease Among Infants and Children --- Use of 13-Valent Pneumococcal Conjugate Vaccine and 23-Valent Pneumococcal Polysaccharide Vaccine: Recommendations of the Advisory Committee on Immunization Practices (ACIP)

机译:预防婴儿和儿童的肺炎球菌疾病---使用13价肺炎球菌结合疫苗和23价肺炎球菌多糖疫苗:免疫实践咨询委员会(ACIP)的建议

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SUMMARY On February 24, 2010, a 13-valent pneumococcal polysaccharide-protein conjugate vaccine (PCV13 [Prevnar 13, Wyeth Pharmaceuticals Inc., marketed by Pfizer Inc.]) was licensed by the Food and Drug Administration (FDA) for prevention of invasive pneumococcal disease (IPD) caused among infants and young children by the 13 pneumococcal serotypes covered by the vaccine and for prevention of otitis media caused by serotypes also covered by the 7-valent pneumococcal conjugate vaccine formulation (PCV7 [Prevnar, Wyeth]). PCV13 contains the seven serotypes included in PCV7 (serotypes 4, 6B, 9V, 14, 18C, 19F, and 23F) and six additional serotypes (serotypes 1, 3, 5, 6A, 7F, and 19A). PCV13 is approved for use among children aged 6 weeks--71 months and supersedes PCV7, which was licensed by FDA in 2000. This report summarizes recommendations approved by the Advisory Committee on Immunization Practices (ACIP) on February 24, 2010, for the use of PCV13 to prevent pneumococcal disease in infants and young children aged The ACIP recommendation for routine vaccination with PCV13 and the immunization schedules for children aged ≤59 months who have not received any previous PCV7 or PCV13 doses are the same as those published previously for PCV7 ( CDC. Preventing pneumococcal disease among infants and young children: recommendations of the Advisory Committee on Immunization Practices [ACIP]. MMWR 2000;49[No. RR-9] ; CDC. Updated recommendation from the Advisory Committee on Immunization Practices [ACIP] for use of 7-valent pneumococcal conjugate vaccine [PCV7] in children aged 24--59 months who are not completely vaccinated. MMWR 2008;57:343--4 ), with PCV13 replacing PCV7 for all doses. For routine immunization of infants, PCV13 is recommended as a 4-dose series at ages 2, 4, 6, and 12--15 months. Infants and children who have received ≥1 dose of PCV7 should complete the immunization series with PCV13. A single supplemental dose of PCV13 is recommended for all children aged 14--59 months who have received 4 doses of PCV7 or another age-appropriate, complete PCV7 schedule. For children who have underlying medical conditions, a supplemental PCV13 dose is recommended through age 71 months. Children aged 2--18 years with underlying medical conditions also should receive PPSV23 after completing all recommended doses of PCV13.
机译:概要2010年2月24日,美国食品药品监督管理局(FDA)批准了一种13价的肺炎球菌多糖蛋白偶联疫苗(PCV13 [Prevnar 13,Wyeth Pharmaceuticals Inc.,由Pfizer Inc.销售])批准用于预防侵入性疫苗涵盖的13种肺炎球菌血清型在婴幼儿中引起的肺炎球菌疾病(IPD),以及由7价肺炎球菌结合疫苗制剂(PCV7 [Prevnar,Wyeth])涵盖的血清型引起的中耳炎的预防。 PCV13包含PCV7中包含的7种血清型(4、6B,9V,14、18C,19F和23F型血清型)和其他6种血清型(1、3、5、6A,7F和19A型血清型)。 PCV13获准在6周至71个月大的儿童中使用,并取代了2000年获得FDA许可的PCV7。本报告总结了2010年2月24日由免疫实践咨询委员会(ACIP)批准的建议预防婴幼儿PCV13肺炎球菌疾病的方法ACIP关于PCV13常规疫苗接种的建议以及未接受任何PCV7或PCV13以前剂量的≤59个月儿童的免疫接种计划与先前针对PCV7公布的相同( CDC。预防婴幼儿肺炎球菌疾病:免疫实践咨询委员会[ACIP]的建议。MMWR 2000; 49 [No。RR-9]; CDC。免疫实践咨询委员会[ACIP]的最新建议在未完全接种疫苗的24--59个月大的儿童中使用7价肺炎球菌结合疫苗[MMV 2008; 57:343--4),用PCV13代替PCV7所有剂量。对于婴儿的常规免疫,建议在2、4、6和12--15个月大时以PCV13的4剂量系列接种。接受≥1剂PCV7的婴儿和儿童应完成PCV13的免疫系列。建议所有接受过4剂PCV7或另一种适合年龄的完整PCV7时间表的14--59个月大的儿童单次补充PCV13。对于患有潜在疾病的儿童,建议在71个月大时补充PCV13剂量。在完成所有推荐剂量的PCV13后,具有基本医疗状况的2--18岁儿童也应接受PPSV23。

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