Use of combination measles, mumps, rubella, and varicella vaccine: recommendations of the Advisory Committee on Immunization Practices (ACIP).

IF 33.7 1区 医学 Q1 Medicine
Mmwr Recommendations and Reports Pub Date : 2010-05-07
Mona Marin, Karen R Broder, Jonathan L Temte, Dixie E Snider, Jane F Seward
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At the time of its licensure, use of MMRV vaccine was preferred for both the first and second doses over separate injections of equivalent component vaccines (MMR vaccine and varicella vaccine), which was consistent with ACIP's 2006 general recommendations on use of combination vaccines (CDC. General recommendations on immunization: recommendations of the Advisory Committee on Immunization Practices [ACIP]. MMWR 2006;55;[No. RR-15]). Since July 2007, supplies of MMRV vaccine have been temporarily unavailable as a result of manufacturing constraints unrelated to efficacy or safety. MMRV vaccine is expected to be available again in the United States in May 2010. In February 2008, on the basis of preliminary data from two studies conducted postlicensure that suggested an increased risk for febrile seizures 5-12 days after vaccination among children aged 12-23 months who had received the first dose of MMRV vaccine compared with children the same age who had received the first dose of MMR vaccine and varicella vaccine administered as separate injections at the same visit, ACIP issued updated recommendations regarding MMRV vaccine use (CDC. Update: recommendations from the Advisory Committee on Immunization Practices [ACIP] regarding administration of combination MMRV vaccine. MMWR 2008;57:258-60). These updated recommendations expressed no preference for use of MMRV vaccine over separate injections of equivalent component vaccines for both the first and second doses. 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Abstract

This report presents new recommendations adopted in June 2009 by CDC's Advisory Committee on Immunization Practices (ACIP) regarding use of the combination measles, mumps, rubella, and varicella vaccine (MMRV, ProQuad, Merck & Co., Inc.). MMRV vaccine was licensed in the United States in September 2005 and may be used instead of measles, mumps, rubella vaccine (MMR, M-M-RII, Merck & Co., Inc.) and varicella vaccine (VARIVAX, Merck & Co., Inc.) to implement the recommended 2-dose vaccine schedule for prevention of measles, mumps, rubella, and varicella among children aged 12 months-12 years. At the time of its licensure, use of MMRV vaccine was preferred for both the first and second doses over separate injections of equivalent component vaccines (MMR vaccine and varicella vaccine), which was consistent with ACIP's 2006 general recommendations on use of combination vaccines (CDC. General recommendations on immunization: recommendations of the Advisory Committee on Immunization Practices [ACIP]. MMWR 2006;55;[No. RR-15]). Since July 2007, supplies of MMRV vaccine have been temporarily unavailable as a result of manufacturing constraints unrelated to efficacy or safety. MMRV vaccine is expected to be available again in the United States in May 2010. In February 2008, on the basis of preliminary data from two studies conducted postlicensure that suggested an increased risk for febrile seizures 5-12 days after vaccination among children aged 12-23 months who had received the first dose of MMRV vaccine compared with children the same age who had received the first dose of MMR vaccine and varicella vaccine administered as separate injections at the same visit, ACIP issued updated recommendations regarding MMRV vaccine use (CDC. Update: recommendations from the Advisory Committee on Immunization Practices [ACIP] regarding administration of combination MMRV vaccine. MMWR 2008;57:258-60). These updated recommendations expressed no preference for use of MMRV vaccine over separate injections of equivalent component vaccines for both the first and second doses. The final results of the two postlicensure studies indicated that among children aged 12--23 months, one additional febrile seizure occurred 5-12 days after vaccination per 2,300-2,600 children who had received the first dose of MMRV vaccine compared with children who had received the first dose of MMR vaccine and varicella vaccine administered as separate injections at the same visit. Data from postlicensure studies do not suggest that children aged 4--6 years who received the second dose of MMRV vaccine had an increased risk for febrile seizures after vaccination compared with children the same age who received MMR vaccine and varicella vaccine administered as separate injections at the same visit. In June 2009, after consideration of the postlicensure data and other evidence, ACIP adopted new recommendations regarding use of MMRV vaccine for the first and second doses and identified a personal or family (i.e., sibling or parent) history of seizure as a precaution for use of MMRV vaccine. For the first dose of measles, mumps, rubella, and varicella vaccines at age 12--47 months, either MMR vaccine and varicella vaccine or MMRV vaccine may be used. Providers who are considering administering MMRV vaccine should discuss the benefits and risks of both vaccination options with the parents or caregivers. Unless the parent or caregiver expresses a preference for MMRV vaccine, CDC recommends that MMR vaccine and varicella vaccine should be administered for the first dose in this age group. For the second dose of measles, mumps, rubella, and varicella vaccines at any age (15 months-12 years) and for the first dose at age >or=48 months, use of MMRV vaccine generally is preferred over separate injections of its equivalent component vaccines (i.e., MMR vaccine and varicella vaccine). This recommendation is consistent with ACIP's 2009 provisional general recommendations regarding use of combination vaccines (available at http://www.cdc.gov/vaccines/recs/provisional/downloads/combo-vax-Aug2009-508.pdf), which state that use of a combination vaccine generally is preferred over its equivalent component vaccines.

使用麻疹、腮腺炎、风疹和水痘联合疫苗:免疫实践咨询委员会(ACIP)的建议
本报告介绍了2009年6月美国疾病控制与预防中心免疫实践咨询委员会(ACIP)通过的关于使用麻疹、腮腺炎、风疹和水痘联合疫苗(MMRV、ProQuad、默克公司)的新建议。MMRV疫苗于2005年9月在美国获得许可,可用于替代麻疹、腮腺炎、风疹疫苗(MMR, M-M-RII,默克公司)和水痘疫苗(VARIVAX,默克公司),以实施推荐的2剂疫苗计划,在12个月至12岁的儿童中预防麻疹、腮腺炎、风疹和水痘。在获得许可时,首选第一剂和第二剂使用MMRV疫苗,而不是单独注射等效成分疫苗(MMR疫苗和水痘疫苗),这与ACIP 2006年关于使用联合疫苗的一般建议(CDC)一致。关于免疫的一般建议:免疫实践咨询委员会的建议。MMWR 2006; 55;[不。RR-15])。自2007年7月以来,由于与有效性或安全性无关的生产限制,MMRV疫苗的供应暂时无法获得。MMRV疫苗预计将于2010年5月再次在美国上市。2008年2月,根据获得许可后进行的两项研究的初步数据,接种第一剂MMRV疫苗的12-23月龄儿童与同一次访问分别接种第一剂MMR疫苗和水痘疫苗的同龄儿童相比,接种疫苗后5-12天发生发热性癫痫的风险增加,ACIP发布了关于MMRV疫苗使用的最新建议(CDC)。更新:免疫实践咨询委员会[ACIP]关于MMRV联合疫苗接种的建议。MMWR 2008; 57:258-60)。这些更新后的建议并不表示在第一剂和第二剂中使用MMRV疫苗比单独注射等效成分疫苗更有优势。两项许可后研究的最终结果表明,在12- 23个月的儿童中,每2,300-2,600名接种第一剂MMRV疫苗的儿童与在同一次就诊中分别接种第一剂MMR疫苗和水痘疫苗的儿童相比,在接种疫苗后5-12天发生一次额外的发热性癫痫发作。许可后研究的数据并未表明,接种第二剂MMRV疫苗的4- 6岁儿童与在同一次就诊时分别接种MMR疫苗和水痘疫苗的同龄儿童相比,接种疫苗后出现发热性癫痫发作的风险增加。2009年6月,在考虑了许可后的数据和其他证据后,ACIP通过了关于使用第一剂和第二剂MMRV疫苗的新建议,并确定了个人或家庭(即兄弟姐妹或父母)癫痫发作史,作为使用MMRV疫苗的预防措施。对于12- 47个月大的麻疹、腮腺炎、风疹和水痘疫苗的第一剂,可以使用MMR疫苗和水痘疫苗或MMRV疫苗。考虑接种MMRV疫苗的提供者应与父母或照顾者讨论两种疫苗接种方案的益处和风险。除非父母或照顾者表达对MMRV疫苗的偏好,疾病预防控制中心建议在该年龄组中应首次接种MMR疫苗和水痘疫苗。对于任何年龄(15个月至12岁)的麻疹、腮腺炎、风疹和水痘疫苗的第二剂和年龄>或=48个月的第一剂,通常优选使用MMRV疫苗,而不是单独注射其等效成分疫苗(即MMR疫苗和水痘疫苗)。该建议与ACIP 2009年关于使用联合疫苗的临时一般建议(可在http://www.cdc.gov/vaccines/recs/provisional/downloads/combo-vax-Aug2009-508.pdf获得)一致,该建议指出,使用联合疫苗通常优于其等效成分疫苗。
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来源期刊
Mmwr Recommendations and Reports
Mmwr Recommendations and Reports PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH-
CiteScore
36.00
自引率
0.00%
发文量
3
期刊介绍: The MMWR series of publications is published by the Office of Science, Centers for Disease Control and Prevention (CDC), U.S. The MMWR Recommendations and Reports contain in-depth articles that relay policy statements for prevention and treatment in all areas in the CDC’s scope of responsibility (e.g., recommendations from the Advisory Committee on Immunization Practices).
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