23 research outputs found

    Vaccine safety issues at the turn of the 21st century

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    Global gains in vaccination coverage during the early 21st century have been threatened by the emergence of antivaccination groups that have questioned the effectiveness of vaccines to generate public distrust of vaccines and immunisation programmes. This manuscript summarises six key topics that have been at the centre of global discussions on vaccine safety during the early 21st century: thiomersal in multi-dose non-live vaccines, aluminium adjuvants used with several non-live vaccines, autism and auto-immune conditions as possible consequences of vaccination, a risk of immune overload with increasing numbers of vaccinations, and detrimental non-specific effects (NSEs) of vaccination. For each topic, we describe the hypothesis behind the public concern, the evidence reviewed by the WHO's Global Advisory Committee for Vaccine Safety (GACVS) during 1999-2019, and any significant new data that has emerged since GACVS conclusions were made. Although the scientific evidence on these issues overwhelmingly supports the safety of vaccines, communication messages to caregivers and providers need to condense and convey scientific information in an appropriate way to address concerns contributing to vaccine distrust. In addition, there is need for further studies specifically designed to address both positive and negative NSE of vaccination. The role of GACVS will be increasingly important in evaluating the evidence and engaging the global community in promoting and assuring the safety of vaccines in the decades to come as we move into an era in which we use new vaccination platforms, antigens and formulations

    Chapter 15, Surveillance Indicators: 15--1 Chapter 15: Surveillance Indicators

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    le of contacts around each case was identified and vaccinated, creating a wall of immunity around the remaining cases, and leading ultimately to the global eradication of smallpox. 3 This could not have been achieved without recognition of the need for an additional strategy, and that new strategy could not have been implemented without the ability to rapidly identify and respond to individual cases. As Andrews and Langmuir wrote in 1963, "to achieve and maintain the eradication status of a specific disease within an area, it is necessary 1) to obstruct transmission until endemicity ceases, and 2) to prevent of nullify the reestablishment of the disease from carriers, relapsing cases, or imported sources of infection. Accordingly, an adequate surveillance organization must be developed to identify and cope with these threats to the achievement of disease eradication." 4 In routine disease control programs, routine disease surveillance systems are usually adequate to meet program de

    Diphtheria in the Former Soviet Union: Reemergence of a Pandemic Disease

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    The massive reemergence of diphtheria in the Newly Independent States of the former Soviet Union marked the first large-scale diphtheria epidemic in industrialized countries in 3 decades. Factors contributing to the epidemic included a large population of susceptible adults; decreased childhood immunization, which compromised what had been a well-established childhood vaccination program; suboptimal socioeconomic conditions; and high population movement. The role of a change in the predominant circulating strains of Corynebacterium diphtheriae in this epidemic remains uncertain. Massive, well-coordinated international assistance and unprecedented efforts to vaccinate adults were needed to control the epidemic

    Chapter 20: National Surveillance of Vaccine-Preventable Diseases

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    mily members and other contacts were included. Case reports were transmitted by telephone or telegraph to the Poliomyelitis Surveillance Unit where the data were collated, analyzed, and disseminated via poliomyelitis surveillance reports; the first report was mailed out on May 1, 1955---only 3 days after the surveillance activity was initiated. The report was prepared and distributed daily for 5 weeks, weekly for the remainder of the summer and fall, and once every 3--4 weeks during the winter. During the first days of the surveillance program, as more cases were reported, the data demonstrated with increasing certainty that the problem was confined to vaccine produced by a single manufacturer. Production procedures were reviewed and other manufacturers were encouraged to continue vaccine production. Without the surveillance program and the rapid clarification of the scope of the problem that was provided by the analysis of national surveillance data, the manufacture of poliomyelitis
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