Sutter R W, Prevots D R, Cochi S L
Vaccine Preventable Disease Eradication Division, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Pediatr Clin North Am. 2000 Apr;47(2):287-308. doi: 10.1016/s0031-3955(05)70208-x.
Poliomyelitis prevention in the United States has relied virtually exclusively on OPV during the past 30 years. Starting in 1997, a major change in the poliomyelitis vaccination policy occurred, facilitated by substantial progress toward worldwide poliomyelitis eradication. A sequential schedule of IPV followed by OPV became the preferred means to prevent poliomyelitis, although an all-OPV and an all-IPV schedule were considered acceptable alternatives. In 1999, two doses of IPV were recommended to start the primary series, followed by two doses of either poliovirus vaccine. As of January 2000, an all-IPV schedule is currently being implemented in the United States for routine childhood vaccination. Several unusual features are associated with the major public health policy change from an all-OPV to a sequential schedule, including (1) the process of involving a neutral party (i.e., the IOM); (2) the perceived concerns expressed before the change in policy with regard to provider and parent compliance, which could affect the hard-earned gains in raising immunization coverage rates; (3) the ethical issues surrounding the change (e.g., societal versus individual protection) and the influence that a single case of VAPP may have on national policy; (4) the relative lack of importance of cost-effectiveness data; and (5) the weight of progress in the global polio eradication initiative spurring the change in the United States and, increasingly, in other industrialized countries. The IOM assisted in the evaluation of the national poliomyelitis vaccination policy in 1977 and again in 1988. The 1988 review recommended that a sequential IPV-OPV schedule be considered at such time that a combination vaccine becomes available. Also, the IOM raised several important questions. Extensive research to address the questions raised by the IOM had been conducted so that, in 1996, more data were available for the decision-making process. The primary reasons for the change in vaccination policy were (1) the continued occurrence of VAPP in the absence of indigenously acquired wildtype poliovirus-associated paralytic disease, (2) the reduced risk for importation and spread of wild-type poliovirus caused by the progress of the global polio eradication initiative, (3) evidence from vaccine trials that combined IPV-OPV schedules are safe and immunogenic, and (4) maintenance of high levels of population immunity to poliovirus. The global effect of a national change in poliomyelitis vaccination policy was also considered in this policy-making process. Some members of the public health and medical communities raised objections that an increased reliance on IPV in the United States could lead other countries, especially developing countries, to inappropriately abandon OPV and increase reliance on IPV for routine vaccination. Experience from the global smallpox eradication campaign indicated that this scenario was unlikely. The United States ceased vaccinating against smallpox in 1971, 6 years before smallpox was eliminated from the world, without jeopardizing the global smallpox campaign. Subsequently, the effect on the global eradication initiative has been negligible. This article illustrates the potential discrepancy between expressed theoretic concerns about the number of injections and the actual practice once vaccination policy recommendations become the standard of care and that appropriate training and education can overcome these initial concerns. The authors found that compliance with the recommended use of IPV for the first and second doses as part of the sequential schedule was high, independent of socioeconomic status and ethnicity. The need for additional injections did not present a barrier to completion of the recommended childhood immunization schedule. (ABSTRACT TRUNCATED)
在过去30年里,美国的脊髓灰质炎预防几乎完全依赖口服脊髓灰质炎疫苗(OPV)。从1997年开始,随着全球根除脊髓灰质炎工作取得重大进展,脊髓灰质炎疫苗接种政策发生了重大变化。先接种灭活脊髓灰质炎疫苗(IPV)再接种OPV的序贯接种程序成为预防脊髓灰质炎的首选方法,不过全OPV和全IPV接种程序也被视为可接受的替代方案。1999年,建议用两剂IPV开始基础免疫程序,随后再接种两剂任何一种脊髓灰质炎病毒疫苗。截至2000年1月,美国目前在儿童常规免疫接种中实施全IPV接种程序。从全OPV接种程序到序贯接种程序这一重大公共卫生政策变化有几个不同寻常的特点,包括:(1)有一个中立机构(即医学研究所)参与其中;(2)在政策改变之前人们对医护人员和家长依从性的担忧,这可能会影响来之不易的提高免疫接种覆盖率的成果;(3)围绕这一变化的伦理问题(如社会保护与个人保护)以及一起疫苗相关麻痹型脊髓灰质炎(VAPP)病例可能对国家政策产生的影响;(4)成本效益数据相对缺乏重要性;(5)全球根除脊髓灰质炎行动取得的进展推动了美国乃至越来越多其他工业化国家的这一政策变化。医学研究所曾在1977年和1988年协助评估国家脊髓灰质炎疫苗接种政策。1988年的审查建议,在联合疫苗可用时考虑采用IPV - OPV序贯接种程序。此外,医学研究所还提出了几个重要问题。为解决医学研究所提出的问题进行了广泛研究,因此在1996年有了更多数据用于决策过程。疫苗接种政策改变的主要原因是:(1)在没有本土获得的野生型脊髓灰质炎病毒相关麻痹性疾病的情况下,VAPP仍持续发生;(2)全球根除脊髓灰质炎行动取得进展,野生型脊髓灰质炎病毒输入和传播的风险降低;(3)疫苗试验证据表明IPV - OPV序贯接种程序安全且具有免疫原性;(4)人群对脊髓灰质炎病毒保持高水平免疫力。在这一决策过程中还考虑了国家脊髓灰质炎疫苗接种政策变化的全球影响。一些公共卫生和医学界人士提出反对意见,认为美国增加对IPV的依赖可能导致其他国家,特别是发展中国家不适当地放弃OPV并增加对IPV进行常规接种的依赖。全球根除天花运动的经验表明这种情况不太可能发生。美国在1971年停止接种天花疫苗,比全球根除天花早6年,且未危及全球天花防治运动。随后,对全球根除行动的影响微乎其微。本文说明了在疫苗接种政策建议成为标准治疗方法后,关于注射次数的理论担忧与实际做法之间可能存在差异,以及适当的培训和教育可以克服这些最初的担忧。作者发现,作为序贯接种程序一部分,第一剂和第二剂按建议使用IPV的依从性很高,与社会经济地位和种族无关。额外注射的需求并未成为完成建议的儿童免疫接种程序的障碍。(摘要截断)