Open session of the standing technical committee of the EUFMD- 2004

Page 477

Appendix 78 Policy and science of FMD control: the stakeholders’ contribution to decision making. A call for Integrated Animal Disease Management Mary Marshall* and Paul Roger: Animal Health Resources Ltd. Registered office: St. John’s House, 5 South Parade, Summertown, Oxford OX2 7JL, U.K Abstract Effective control of foot-and-mouth disease (FMD) - prevention, surveillance and response - requires integrated animal disease management as a cooperative effort between stakeholders, scientists and decision makers, at all levels: local, national, regional and international. This paper suggests a process and outlines specific critical issues that need to be addressed in order to best use the science and technology that is available now and to develop new technologies that will lead to significant improvements. The overall objective is not to allow the disease or the disease control measures to damage, violate or destroy public health, the environment, or the economy, or to allow politics to drive disease control policies at the expense of the ethical relationship between man and animals. Critical issues of prevention, surveillance and response policies are examined, and specific recommendations are made to reduce the risk or effect of natural and deliberate introductions. For prevention: a) rapid portable diagnostics and provision of vaccines to control and eradicate the reservoirs of disease and b) alerts, leading to increased controls at borders, animal movement restrictions and biosecurity on farms. For surveillance: a) reporting of unusual symptoms, rapid diagnostics and identification of patterns, b) enhanced role of GIS linked to an IT system, and c) collection, storage and sharing of disease information. For response policies: a) the role and implementation of stamping out and of vaccination, and b) simulation exercises with stakeholder participation. For all aspects of FMD control, consideration should be given to: a) the composition, responsibilities and role of the balanced, permanently operational Expert Group in EU member states as specified in the EU FMD Directive, b) establishment of a balanced, permanently operational European Expert Group, and c) establishment of both a European and an International FMD Task Force. Stakeholders need access to accurate, up-to-date, unbiased information about the science of disease control, how the technologies work and can be used, and an assurance that the technologies best fit for the required purpose will be used. Researchers need to work together to avoid duplications and gaps in their research and to recognize the benefit of new, and sometimes innovative, technologies. They also need feedback from stakeholders on the acceptability and best use of the technologies. A process to achieve these goals through an EU funded collaborative research project will be described. Introduction Stakeholders are defined as all those who have a direct or indirect interest in FMD due to the impact of the disease on their or their animals’ lives. This involves a cross-section of the population, ranging from those with extensive knowledge of livestock to those who have little or no knowledge or education concerning the complexity of the issues. The recommendations in this paper are based on information gathered from open meetings, private consultations and extensive internet communications, with a wide and geographically dispersed range of stakeholders, scientists and policy makers that began in February 2001 when FMD was identified in the UK. The views of stakeholders must be taken seriously because their cooperation is essential in the implementation of an effective and ethical scientific disease control process and because they represent large and diverse political pressure groups. They are increasingly vocal, often with little consensus amongst the varying interests they represent, and need to be persuaded that the control measures are appropriate, proportionate and necessary. If they say that certain measures are unacceptable, the policy makers must take their concerns into account. In order for control policies to be undertaken in a cooperative manner, it is imperative that stakeholders have access to the most objective and accurate information about the underlying science and that the implications are clearly explained and open to effective consultations and debate. Consultation exercises must be easy to access, genuine and transparent. The role of scientists is central in the process to determine: • How we can use the science and technology that is available now in rapid, effective, proportionate and acceptable control. • How we can develop new technologies and new approaches using these technologies to improve control. The overall objective is not to allow the disease or the disease control measures to: • Damage, violate or destroy public health, the environment, or the economy, or

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Appendix 82

17min
pages 492-500

Appendix 77

22min
pages 468-476

Appendix 78

25min
pages 477-484

Appendix 79

14min
pages 485-489

Appendix 81

1min
page 491

Appendix 80

1min
page 490

Appendix 76

12min
pages 464-467

Appendix 75

1min
page 463

Appendix 64

10min
pages 412-414

Appendix 72

13min
pages 455-460

Appendix 73

1min
page 461

Appendix 65

1min
page 415

Appendix 67

1min
page 424

Appendix 63

34min
pages 401-411

Appendix 62

2min
page 400

Appendix 54

8min
pages 361-363

Appendix 61

15min
pages 394-399

Appendix 55

11min
pages 364-366

Appendix 59

1min
page 385

Appendix 60

20min
pages 386-393

Appendix 56

1min
page 367

Appendix 42

21min
pages 270-276

Appendix 52

10min
pages 350-352

Appendix 50

21min
pages 330-339

Appendix 46

2min
page 307

Appendix 37

7min
pages 241-243

Appendix 38

7min
pages 244-246

Appendix 41

2min
page 269

Appendix 40

15min
pages 255-268

Appendix 36

16min
pages 236-240

Appendix 35

15min
pages 231-235

Appendix 34

25min
pages 224-230

Appendix 28

2min
page 198

Appendix 31

10min
pages 212-215

Appendix 29

16min
pages 199-203

Appendix 33

3min
pages 221-223

Appendix 27

1min
page 197

Appendix 26

27min
pages 188-196

Appendix 25

12min
pages 182-187

Appendix 23

8min
pages 168-171

Appendix 22

28min
pages 158-167

Appendix 15

2min
page 113

Appendix 16

7min
pages 114-116

Appendix 20 EMEA paper extract - Recommendations for tests for induction of antibodies to NSP antigens by FMD vaccines

4min
pages 144-145

Appendix 19

18min
pages 136-143

Appendix 14

4min
page 112

Appendix 13

10min
pages 107-111

Appendix 5

2min
page 64

Appendix 12

9min
pages 104-106

Appendix 3

9min
pages 47-49

Appendix 4

26min
pages 50-63

Appendix 8

12min
pages 77-80

Appendix 2

8min
pages 43-46

Open Session

6min
pages 39-42

Closed Session

2min
pages 37-38

Item 11 – Persistent and subclinical infections – diagnostic and surveillance issues

3min
page 33

Item 15 – Managing the decision-making process in control of FMD and in the priority setting of research and development

3min
page 36

Item 14 – Regulatory compliance

2min
page 35

Item 10 – International issues

3min
page 32

Item 9 – Novel vaccines

3min
page 31

Item 7 – Optimisation of conventional vaccines

3min
page 29

Item 4 – Managing diagnostic demands

3min
page 27

Item 8 – Regulatory issues affecting FMD vacine selection and use

3min
page 30

Item 3 – Transmission and its control

3min
page 26

3.4.2 Post-vaccination serosurveillance (PVS) for presence of FMD infected animals

3min
page 16

Item 1 – Recent findings in molecular epidemiology of FMDV

3min
page 24

Item 2 – Surveillance: for what purpose and how much is enough?

3min
page 25

4.2 Collection of sera/specimens for validation of DIVA tests for detection of animals received from SAT virus infection

3min
page 20
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Open session of the standing technical committee of the EUFMD- 2004 by EuFMD - Issuu