Hostname: page-component-7c8c6479df-7qhmt Total loading time: 0 Render date: 2024-03-29T04:32:12.840Z Has data issue: false hasContentIssue false

Contribution of Meat Inspection to the surveillance of poultry health and welfare in the European Union

Published online by Cambridge University Press:  18 December 2014

A. HUNEAU-SALAÜN*
Affiliation:
ANSES, Ploufragan-Plouzané Laboratory, Ploufragan, France
K. D. C. STÄRK
Affiliation:
SAFOSO Inc., Bern, Switzerland Royal Veterinary College, Hertfordshire, UK
A. MATEUS
Affiliation:
SAFOSO Inc., Bern, Switzerland Royal Veterinary College, Hertfordshire, UK
C. LUPO
Affiliation:
IFREMER, SG2M-LGPMM, La Tremblade, France
A. LINDBERG
Affiliation:
National Veterinary Institute, Uppsala, Sweden
S. LE BOUQUIN-LENEVEU
Affiliation:
ANSES, Ploufragan-Plouzané Laboratory, Ploufragan, France
*
*Author for correspondence: Dr A. Huneau-Salaün, ANSES, BP53, 22440 Ploufragan, France. (Email: adeline.huneau@anses.fr)
Rights & Permissions [Opens in a new window]

Summary

In the European Union, Meat Inspection (MI) aims to protect public health by ensuring that minimal hazardous material enters in the food chain. It also contributes to the detection and monitoring of animal diseases and welfare problems but its utility for animal surveillance has been assessed partially for some diseases only. Using the example of poultry production, we propose a complete assessment of MI as a health surveillance system. MI allows a long-term syndromic surveillance of poultry health but its contribution is lowered by a lack of data standardization, analysis and reporting. In addition, the probability of case detection for 20 diseases and welfare conditions was quantified using a scenario tree modelling approach, with input data based on literature and expert opinion. The sensitivity of MI appeared to be very high to detect most of the conditions studied because MI is performed at batch level and applied to a high number of birds per batch.

Type
Original Papers
Copyright
Copyright © Cambridge University Press 2014 

INTRODUCTION

From the past to the present: why does Meat Inspection (MI) need to evolve?

MI is a control process commonly described as a set of tasks performed at slaughterhouses and sometimes at farms to ensure that animals entering the food chain comply with the legal hygiene requirements for human consumption. The major aim of MI is therefore to protect the public from hazards, such as infectious agents, that could be transmitted or carried by meat (contamination).

The increasing burden of foodborne illnesses and the rapid changes in food production and food exchanges throughout the world led the Food and Agriculture Organization and the World Health Organization to propose guidelines for strengthening food control systems [1]. Taking into account this international context, a new European legislation, relying on the White Paper on Food Safety published in 2000, has been developed. It aims to base food control systems on an integrated ‘farm-to-fork’ approach and on a risk analysis process. The White Paper was the stepping stone for the three Hygiene Regulations known as the Hygiene Package, that deal with all foods and that cover the entire food chain [Reference Dwinger2]. In the Hygiene Package, Regulation 854/2004 lays down specific rules for the organization of official controls on animal products [3].

The first conclusions on the application of this regulation drawn by the chief veterinary officers of the European Member States in 2008 showed that a modernization of sanitary inspection in slaughterhouses was needed to fully exploit benefits from a risk-based approach. Consequently, the European Commission [4] mandated the European Food Safety Authority (EFSA) to evaluate the capacity of current MI to assess the fitness of meat for human consumption and, if needed, to propose modifications to ensure an appropriate level of public health protection (Mandate 1005) [5]; the questions had to be considered separately for the main animal production systems in Europe, including poultry. As the main public health hazards in poultry products could not be detected by the current visual MI [6], proposed changes in MI procedures were expected to be important. In addition to the protection of public health, MI also contributes to animal health and welfare surveillance by detecting and monitoring disease syndromes and welfare problems that are not reported at the farm level. The EFSA panel on Animal Health and Animal Welfare (AHAW) was mandated to assess the potential consequences on animal health and welfare surveillance of the changes in the current MI system proposed by the other EFSA panels.

The objective of our paper was to present findings of this assessment and to demonstrate how this evaluation evolved from an empirical and practical experience to a global and quantitative assessment. This paper focuses only on poultry species but reports on other species have been published on the EFSA website (http://www.efsa.europa.eu, topic Meat Inspection). First, a literature review will describe the past experiences demonstrating the contribution of the current MI procedures to poultry health surveillance. Second, the methodology and the main results will be shown. Elements dealing with the impact of the modernization of MI on poultry health surveillance can be found elsewhere [6].

SURVEILLANCE OF ANIMAL HEALTH AND WELFARE DURING THE CURRENT MI PROCEDURE

The current MI procedure in the European Union is described for all species in Annex I of Regulation 854/2004 [7] with special dispositions for poultry species in Section IV, Chapter V. The epidemiological unit of interest in MI is a batch of poultry, i.e. poultry reared on the same holding and sent to slaughter in a single transport. The MI for poultry comprises three inspection tasks carried out under the supervision of the Official Veterinarian (OV). MI tasks can be delegated to official auxiliaries operating under the supervision of the OV (Annex I, Section III, Chapter III and part A). In poultry and lagomorph abattoirs, these auxiliaries may be from the slaughterhouse staff provided that the inspection staff acts independently from the production staff and they receive appropriate training provided by the official veterinary authorities.

Food chain information

The first step in MI is devoted to checking and analysing food chain information (FCI), i.e. relevant information on animals' identification and on animals' health transmitted from the holding of provenance. Required FCI is described in Annex II, Section III of Regulation 853/2004 [7]; most of the Member States collect harmonized FCI at national level via a standardized declaration form. FCI has to be transmitted to the OV at least 24 h before slaughtering, when the ante-mortem inspection is performed at the abattoir. If the birds have been inspected at the farm of origin, FCI can be provided before unloading the batch in the slaughterhouse. FCI is based on declarations of farmers and food business operators (FBO). The reliability of FCI might be questionable. However Lupo et al. [Reference Lupo8] concluded that FCI transmitted to slaughterhouses was concordant with on-farm observations collected by independent investigators. FCI analysis is a direct application of the risk-based approach because results from FCI have to be taken into account to adapt the thoroughness of the inspection process accordingly to the health status of the batch. The study of Lupo et al. [Reference Lupo9] showed that FCI was relevant to identify batches of broilers with a high risk of sanitary condemnation, demonstrating the usefulness of FCI for a risk-based MI. Various measures can be taken in response to the estimated risk of condemnation shown by a batch of poultry, e.g. slowing down the slaughter line speed to allow in-depth inspection. In France, an experimental programme is presently conducted to define a standardized frame of application of the risk-based inspection and to estimate its practicality under commercial conditions [Reference Allain10].

Ante-mortem inspection (AMI)

The second inspection task is the AMI which takes place at slaughterhouse in most of the Member States but can be also performed on farm for poultry species. AMI mainly aims to detect any sign indicating that animal welfare has been compromised during handling and transport or that animals are affected by conditions likely to adversely affect animal or human health. In particular, stress caused by loading and transport may enhance the expression of clinical signs in animals suffering from a disease at incubation or subclinical stages. There are 2–3 points of control for AMI [Reference Löhren11]; inspection in crates, inspection after unloading and inspection after stunning. Only a sample of crates is inspected before unloading but all birds are individually observed during the manual shackling. AMI is the key stage for monitoring welfare conditions relative to handling and transport of poultry (e.g. dead on arrival, thermal comfort during transport) but Regulation 854/2004 also states that special attention should be observed during AMI for the detection of diseases on the OIE list [12]. For instance, avian botulism can only be detected during the inspection of live birds due to its pathognomonic clinical signs (flaccid paralysis of the neck, wings and/or legs) as no visible lesion can be detected during post-mortem inspection (PMI).

Post-mortem inspection

The third task is the PMI of the whole plucked carcass, the viscera and the carcass after evisceration (including the body cavity). PMI is designed to detect and withdraw from the food chain carcasses showing grossly identifiable abnormalities that may affect their safety or wholesomeness; special attention should be also placed on the detection of zoonotic diseases and of diseases classified in the OIE list [12]. By contrast to previous inspection tasks that are mostly done at batch level, PMI is performed at the individual level implying that all carcasses are to be inspected. PMI leads to condemnation of carcasses or parts of them that are judged to be unfit for human consumption, based on a visual inspection. Reasons for carcass condemnation are not explicitly described in Regulation 854/2004 but possible origins of unfit meat are exhaustively listed. Condemnation for poultry carcasses is based on visual macroscopic criteria that are rarely pathognomonic. As an example, the most frequent reasons for condemnation in broiler and turkey broiler batches in France are emaciation and congestion, which are generic terms concordant with a large spectrum of diseases and conditions [Reference Lupo13, Reference Lupo14]. A few infectious or parasitic diseases may lead to pathognomonic lesions enabling a direct diagnosis during PMI. For instance, histomoniasis (Histomonas meleagridis) sometimes leads to characteristic round lesions on liver that could be detected during manual evisceration [Reference Grist15] but birds affected at such an advanced stage of the disease are normally unfit for slaughter. Avian tuberculosis (Mycobacterium avium) is a chronic infection with a protracted course that may go unnoticed at the farm but typical tubercular granulomata can be easily detected on the spleen and liver during PMI [Reference Jordan and Jordan16]. Nevertheless, a reason for condemnation is generally given with no inference on the aetiology of the lesions. As an example, in a study on carcasses condemned for skin lesions, Fallavena et al. [Reference Fallavena17] concluded that cutaneous macroscopic changes as observed at PMI were not specific and did not allow accurate identification of skin diseases.

SPECIFIC CONTRIBUTION OF CURRENT MI TO POULTRY HEALTH AND WELFARE SURVEILLANCE

A two-way information flow: an opportunity for poultry health surveillance

Regulation 854/2004 requires transmission of the results from MI to the FBOs and to the primary producer when the detected problems may be related to rearing conditions. This disposition establishes the principle of a two-way information flow: from the farm to the slaughterhouse by FCI, and from the abattoir to the farm by transmission of MI results. There are some practical examples of benefits from feedback transmission of MI observations. A pilot study reported by Ansong-Danquah et al. [Reference Ansong-Danquah18] was conducted in a Canadian abattoir during 5 years in 1980s, with a systematic feedback of MI results to farmers and to broiler companies. During the first 2 years, lesions caused by Marek's disease were the primary cause of carcass condemnations, underlining insufficient vaccination coverage of the broiler population. Vaccination programmes were therefore reinforced by the broiler companies and condemnations for lesions due to Marek's disease were no longer relevant during the final 3 years of the experiment.

Integration of welfare surveillance

The recent evolution of the assessment of animal welfare towards the monitoring of animal-based welfare indicators [19] gives a new dimension to PMI. As demonstrated in the Welfare Quality project [20], animal-based welfare-outcome indicators related to body condition in poultry can be more easily and more accurately monitored during PMI than on farm. This is the case for injuries, haematomas, scratches, foot-pad dermatitis, hock burns and breast blisters, which are more visible on shackled and plucked carcasses. Ascites characterized by an accumulation of liquid in the body cavity is also better detected during PMI than on farm or at AMI. These conditions provide information on welfare during handling and transport but also on welfare during rearing, since most of the indicators are significantly associated with on-farm factors [Reference Gouveia, Vaz-Pires and Martins da Costa21, Reference Allain22]. The Swedish Broiler Welfare Programme demonstrates that the regulation of broiler density during rearing, based on the prevalence of foot-pad dermatitis observed during PMI, can reduce the incidence of this problem [Reference Ekstrand23, Reference Berg, Weeks and Butterworth24].

The implementation of Directive 2007/43/EC on broiler protection will generalize the use of PMI for collection of animal-based welfare indicators; results from PMI become one of the key indicators to allow derogation to the maximum stocking density during rearing.

Concrete examples of MI contribution to poultry health surveillance

Despite the fact that the main aim of MI is to protect public health from foodborne hazards, it also allows the monitoring of animal health and welfare. This system can both contribute to the detection of cases of an emerging or re-emerging animal disease and to the monitoring of the prevalence of endemic diseases and welfare conditions. Although these contributions to animal health surveillance are potentially high, there are few examples in the literature clearly demonstrating the value of MI in this context (Table 1). Most of these studies rely on an in-depth PMI, sometimes completed by histological and bacteriological analysis. Furthermore, outputs of these studies are rarely analysed in any other way than the economic impact of condemnations for producers and FBOs. Discussions proposed by the authors on the contribution of MI to animal health surveillance are summarized in Table 1.

Table 1. Examples of studies using Meat Inspection (MI) for monitoring health and welfare in poultry in Europe, North America, South America, Middle East and Asia. Classification of the studies according to their objectives: ‘case report’ (description of a new condition), ‘prevalence’ (assessment of condition prevalence and its temporal evolution), ‘aetiology’ (identification of the aetiology of a condition) and ‘risk factors’ (identification of factors associated with the occurrence of a condition)

AMI, Ante-mortem inspection; PMI, Post-mortem inspection.

A relevant experience of the MI contribution to poultry health surveillance is the emergence of cellulitis in North America. At the end of 1990s, a sharp increase in carcass condemnations was detected in Canadian poultry abattoirs [Reference Kumor25], due to a new kind of skin lesion classified as cellulitis. Examination of condemned carcasses of broilers and turkeys enabled the precise description of this condition, which was not visible on animals at farm nor at AMI as it is a subclinical syndrome [Reference Olkowski26]. A monitoring programme of the percentage of carcass condemnations for cellulitis was consequently started in federal abattoirs. This programme allowed quantification of the increasing incidence of cellulitis during the following years [Reference Saint-Hilaire and Sears27]. Observations during PMI were also used to classify batches according to their level of condemnation for cellulitis; this classification was the basis for an analytical epidemiological survey to identify risk factors for cellulitis on poultry farms [Reference Elfadil, Vaillancourt and Meek28].

ASSESSING THE CONTRIBUTION OF MI TO POULTRY HEALTH AND WELFARE SURVEILLANCE IN EUROPE

Qualitative assessment of the contribution of MI to poultry health surveillance

Surveillance is defined as a systematic ongoing collection, aggregation, and analysis of data and the timely transmission of information to the risk manager in order to take mitigation measures [Reference Hoinville29]. MI can be considered as a component of a syndromic surveillance performed at slaughter level: FCI, clinical signs and gross lesions are used to monitor various health hazards, without further diagnosis. Table 2 provides a list of criteria to assess the quality of a surveillance system, adapted from Salman et al. [Reference Salman, Stärk and Zepeda30], and its application to the current MI system in poultry. Most of the quality criteria can be assessed from a complete description of MI procedures, as carried out by Löhren [Reference Löhren11], but estimation of sensitivity and positive predictive value could only be obtained by experiment [Reference Fisher, Trampel and Griffith31] or by modelling using methods such as latent classes [Reference Enoe32, Reference Bonde33] or decision-tree scenarios.

Table 2. Qualitative assessment of Meat Inspection (MI) as a surveillance component for health and welfare surveillance in poultry in the European Union (adapted from Salman et al. [Reference Salman, Stärk and Zepeda30])

Despite this lack of available data on performance, quality assessment was used to produce a short Strength-Weakness-Opportunity-Threat (SWOT) analysis of MI as a surveillance component (Table 3) [Reference Stärk and Nevel34]. MI is now a long-standing and well-accepted surveillance component in Europe. One of its major strengths is its high representativeness: mortality rates of poultry during rearing are relatively low in the European Union, implying that most of the birds entering production are sent to the abattoir and submitted to MI. MI may be considered as an early-warning surveillance as any modification in the health state of animals could be detected in a timely manner. However emerging or re-emerging diseases are expected to be detected before slaughter (clinical surveillance at farm) and MI is rather the ultimate component of a passive (or reactive) surveillance system, which raises the alarm when the others components fail. The special case of MI in poultry is that the inspection is performed at both batch and bird levels. The global approach at batch level is of interest in animal health surveillance: warning thresholds could be set up for main health indicators and standardized measures proposed in response to the alerts. The use of the MI system for the surveillance of animal health does not add supplementary costs to the expenses already incurred for public health protection; it is therefore an inexpensive way to monitor animal health. Regarding weaknesses, there are basically several technical factors (e.g. speed of the line and lighting) that may interfere with the detection of health problems. The results of MI may also depend on staff experience. A systematic use of AMI observations and condemnation results for health surveillance would require the centralization of results in a harmonized frame of collection and specific staff devoted to results analysis. MI is not an ‘enhanced passive’ surveillance component [Reference Hoinville29], as there is no general and active supervision of MI results in terms of animal health and welfare. In addition to technical constraints and difficulties in data centralization, flexibility of MI is rather low because its general frame is fixed by European and national regulations: any modification to the procedure needs time, staff formation and sometimes financial resources in order for it to be implemented at a national level. The risk-based approach adopted with the Hygiene Package is an opportunity for the optimization of MI as a surveillance component. However the risk-based surveillance only targets the needs for public health protection: the new dispositions may constitute the main threat to the contribution of MI to animal health surveillance.

Table 3. Strength-Weakness-Opportunity-Threat (SWOT) analysis of Meat Inspection (MI) as a surveillance system of animal health and welfare surveillance

FBO, Food business operator; EU, European Union.

Quantitative assessment of the contribution of MI to poultry health surveillance

Methodology. The assessment of sensitivity, i.e. the probability of detecting cases, remains the key element in evaluating the performance of MI as a health surveillance system [Reference Hathaway and Richards35]. We used quantitative decision-tree scenario models to evaluate the sensitivity of MI as an animal surveillance system, parameterized with data from the literature if available or by expert opinion. The approach is described in more detail by Stärk & Nevel [Reference Stärk and Nevel34]. Briefly, the EFSA AHAW panel defined a list of 20 poultry diseases and welfare conditions to be addressed; the prioritization of diseases took into account the relevance of their surveillance at the slaughterhouse, their epidemiologialc characteristics (epizootic or enzootic diseases) and their regulatory and/or economic importance. A bibliographical review was performed to gather data on the prevalence of diseases and welfare conditions at flock level and at the European level and on risk factors associated with these conditions. The review was completed by elicitation of expert opinion to complete gaps in knowledge identified. The elicitation was based on a modified Delphi method as described by Stärk et al. [Reference Stärk36] and the questionnaires used for elicitation are available from the authors upon request.

For each disease or welfare condition, the most affected poultry (species, age and type of production, i.e. egg, meat or breeder) was identified and typical and mild cases described by the experts (Fig. 1). A typical case as seen during MI was defined by a set of symptoms and lesions that are likely to be observed in more than two thirds of birds affected by the given condition and presented for slaughter. A mild case was characterized by more subtle signs than a typical case but was still detectable during MI; it was assumed to be less frequent than a typical case. In a second step of elicitation, experts were asked to provide estimates on the prevalence of affected batches arriving for slaughter, the proportion of typical and mild cases in an affected batch and the probability of detection of a typical case during each step of the MI procedure. The final outcome of the expert elicitation was an estimate (most likely ± range) of the probability of detection under the current MI procedure of a typical case for each of the 20 diseases or welfare conditions.

Fig. 1. Flow diagram of the scenario tree model, with the arrows indicating the order that each step occurs, i.e. node of the tree is calculated. AMI, Ante-mortem inspection; PMI, post-mortem inspection.

Next, the value of MI as a surveillance system was assessed, using two scenario tree models: the ‘freedom of disease’ approach for epizootic diseases [highly pathogen avian influenza (HPAI) and Newcastle disease] and the ‘detection fraction’ approach for other enzootic diseases and welfare conditions [37]. The ‘freedom of disease’ approach measures the ability of a surveillance system to detect one or more infected birds and/or batch of birds if the frequency of the disease is higher than a designed prevalence in the monitored population [Reference Martin, Cameron and Greiner38]. This method then evaluates the capacity of a surveillance system to detect an emerging or re-emerging disease and to give an ‘alert signal’. In the ‘detection fraction’ approach, the value of a surveillance system is assessed by the proportion of cases of the disease detected by the surveillance; this approach is adapted to monitor prevalence of an enzootic disease. In both approaches, the models yield a probability of detection that could be interpreted as the sensitivity of the surveillance system. Consolidated estimates collected during expert elicitation for AMI and PMI were used as input, together with estimates of proportions of case types likely to be presented at the abattoir. The output was estimated by translation of the consolidated estimates into BetaPert distributions, and by using Monte-Carlo simulation (10 000 iterations). Each step of the model represents a node of a tree, and is run in the sequence shown in Figure 1. The most likely and 5th and 95th percentiles of the output distributions of AMI, PMI and the whole inspection process were derived for each disease and condition.

Sensitivity of MI for poultry health and welfare surveillance

The sensitivity of MI for detection of a ‘typical’ case was estimated as high for most of the diseases and conditions studied (Table 4). This high sensitivity has to be examined taking into account some methodological limitations. The methodological development was an on-going process and was not fully consolidated when poultry was considered (one of the first species studied along with pigs). The first limitation was linked to the assumption that the probabilities of detection of abnormalities at each inspection step were independent, leading to a possible underestimation of the detection sensitivity for diseases demonstrating signs detectable at a small number of inspection points, e.g. for botulism or ‘dead on arrival’. In addition, in a risk-based inspection, each inspection step has to be adapted taking into account the results of the previous steps, implying a dependence of the task results. Nevertheless, the sensitivity estimations given separately for each inspection step by the experts [37] suggested that the evaluation of FCI contributed more than the crate inspection to the detection of abnormalities during AMI. During PMI, visual inspection of organs and, to a lesser extent, of the body cavity were considered the most sensitive tasks for disease detection whereas observation of the whole carcass and the feet contributed the most to the detection of welfare problems. Another methodological difficulty was related to the organization of MI for poultry both at batch level (AMI) and at bird level (PMI). The sensitivity of detection of an affected batch (i.e. a batch with a least one affected bird) depended on the sensitivity of detection at bird level and also on the number of animals submitted to MI. Since the size of a poultry batch is generally high (several thousands of birds), the sensitivity of detection at batch level was particularly high for all diseases and conditions. It is therefore expected that the inspection of a large number of animals will always be a very effective way of detecting diseases, even though the sensitivity of detection at the bird level is low.

Table 4. Probabilities of case detection (mode) of ante- and post-mortem inspection procedures at individual bird level (5% and 95% percentiles) for 20 diseases and conditions

Relative contribution of MI to the global animal health surveillance system

In addition to the evaluation of sensitivity of MI to detect diseases and welfare problems, we assessed the relative contribution of MI to animal surveillance compared to other surveillance components existing in the European Union. One epizootic disease (avian influenza; AI), three enzootic diseases (aspergillosis, colisepticaemia, infectious bursal disease; IBD) and one welfare problem (ascites) were considered. For AI, a conventional scenario tree model for freedom of disease was used considering two surveillance components other than MI: clinical surveillance at farm [39] and serological surveillance [40]. The estimated sensitivities at batch level (for a common batch size equal to 10 000 birds) were very high and similar for the three surveillance components considered (Table 5). A scenario tree model has already been used to assess the sensitivity of an AI surveillance system in Canada [Reference Christensen41] and in Catalonia [Reference Alba42]. In these studies, MI was not taken into account in the surveillance system thus its sensitivity was not estimated. This omission suggests that MI is not considered as a means of AI detection, despite that surveillance of OIE list A diseases is one of the MI objectives. Our results showed, however, that MI could be as sensitive as other passive or active components of the surveillance system. It might be worth considering it when evaluating the effectiveness of the overall surveillance system. The Spanish study considered clinical surveillance at farm as a component of the surveillance system; the probability of detecting a batch of broilers infected by HPAI was as high as we estimated in this project for AI in turkeys, but was considerably lower for low pathogenic avian influenza (LPAI). Such a distinction according to AI pathogenicity could not be made in our project because data on epidemiology of HPAI and LPAI are lacking at the European scale.

Table 5. Estimated proportion of turkeys and turkey batches detected as true positives for avian influenza by different surveillance system components

* The combined value does not consider overlap between surveillance system components.

Assumed between-flock prevalence = 0·096, within-flock prevalence = 0·283.

For the four other enzootic conditions, a tree model based on the ‘detection fraction’ approach was developed including MI and clinical surveillance as surveillance components. The detection fraction for colisepticaemia and IBD was estimated to be very high for a batch of 10 000 birds, both for clinical suspicion and MI (Table 6) because the within-flock prevalence at farm was estimated as high by expert opinion (more than 30% of infected birds) and the farmer's and veterinarian's awareness was also expected to be high for these diseases. The benefit of abattoir inspection over farm surveillance was therefore minimal. By contrast, the incremental benefit of MI surveillance over clinical surveillance turned out to be high for ascites. Expert opinion estimated the probability of detection by the farmer to be low (<50%) for this condition: ascites cases are rare in a flock of broilers, occurring mainly at the end of the rearing period when farmers are not prone to ask for a veterinarian visit and the symptoms are usually general and unspecific. The probability of detection of ascites was estimated as very high during PMI, leading to a higher value of MI than clinical surveillance for detecting ascites. For aspergillosis in breeder turkeys, the benefit of MI was also higher than for clinical suspicion but the detected fraction remained very low. This was due to low between- and within- flock prevalences and a high proportion of mild cases, which are more difficult to detect.

Table 6. Detection fraction at batch level (10 000 birds) of selected endemic diseases/conditions by abattoir inspection and clinical suspicion and comparative detection performance with an assumed coverage of 100%

SSC, Surveillance system component.

CONCLUSION

Surveillance of poultry health during MI is an example of a syndromic surveillance, as in most of the cases, no inference can be made on the aetiological cause based on the clinical signs and lesions observed during slaughter. MI enables rapid collection of data on any health event but it does not contribute to early-warning surveillance as it occurs at the last step of the production chain; MI is rather the ultimate component of a passive surveillance system. Nevertheless, the increased use of animal-based welfare indicators in the assessment of poultry welfare confers a new importance on MI, given that these indicators are more easily collected at slaughter than on farm. Despite that, there is a common agreement on its interest, concrete and quantified examples of the contribution of MI to poultry health surveillance are lacking because surveillance data generated by MI are not harmonized at the European level and they are not systematically collected and analysed. However, some past examples show that the two-way information flow from the farm to the slaughterhouse (FCI) and from the slaughterhouse to the farm (MI information) could be effectively used to monitor and even enhance poultry health and welfare. The models proposed to quantify the sensitivity of current MI in the surveillance of both enzootic and epizootic diseases provide a tool which allows the assessment of the potential impact of a revised MI procedure on poultry health surveillance in Europe.

ACKNOWLEDGEMENTS

We acknowledge the contributions of the experts who participated in the expert elicitation exercise. We are also grateful to Mr Georgiev from the Animal Health and Welfare Unit of EFSA and to members of the working group appointed by EFSA to integrate this work to AHAW scientific opinions, particularly to Professor More. This work was supported by EFSA (service contract no. CT/EFSA/AHAW/2010/05).

DECLARATION OF INTEREST

None.

References

REFERENCES

1. FAO/OMS. Assuring Food Safety and Quality: Guidelines for Strengthening National Food Control Systems. FAO Food and Nutrition Paper No. 76, 2002, 84 pp.Google Scholar
2. Dwinger, RH, et al. A brief overview of food hygiene legislation. Deutsche Tieraerztliche Wochenschrift 2007; 114: 294298.Google Scholar
3. FAO. Risk-based food inspection manual. Rome, Italy: Organisation Mondiale des Nations Unies pour l'alimentation et l'agriculture; 2008, 85 pp.Google Scholar
4. European Commission. Report from the Commission to the Council and the European Parliament on the experience gained from the application of the hygiene regulation (EC) No. 852/2004, (EC) No. 853/2004 and (EC) No. 854/2004 of the European Parliament and of the Council of 29 April 2004, 2009.Google Scholar
5. European Commission, Health and Consumers Directorate - General. Requests for a scientific opinion and technical assistance on the public health hazards to be covered by inspection of meat, 2010.Google Scholar
6. EFSA. Scientific Opinion on the public health hazards to be covered by inspection of meat (poultry). EFSA Journal 2012; 10: 2471.Google Scholar
7.Anon. Regulation (EC) No. 854/2004 of the European Parliament and the Council of 29 April 2004 laying down specific rules for the organisation of official controls on products of animal origin intended for human consumption. Official Journal of the European Union 2004; L 139: 206320.Google Scholar
8. Lupo, C. Appreciation of the risk of sanitary condemnation in poultry carcasses ar slaughterhouse based on food chain information: University of Rennes 1, 2009, 323 pp.Google Scholar
9. Lupo, C, et al. Bayesian network as an aid for food chain information use for meat inspection. Preventive Veterinary Medicine 2013; 109: 2536.Google Scholar
10. Allain, V, et al. Health inspection at poultry slaughterhouses: indicators of tasks achievement for veterinary inspection missions. In: World Veterinary Poultry Association Congress. Nantes, France: ISPAIA, 2013, pp. 112.Google Scholar
11. Löhren, U. Overview on current practices of poultry slaughtering and poultry meat inspection: supporting publications EN-298, 2012, 58 pp.Google Scholar
12. OIE. OIE-listed diseases, infections and infestations in force in 2014 (http://www.oie.int/en/animal-health-in-the-world/oie-listed-diseases-2014/). Paris, France: OIE. Accessed 12 May 2014.Google Scholar
13. Lupo, C, et al. Postmortem condemnations of processed broiler chickens in western France. Veterinary Record 2008; 162: 709713.Google Scholar
14. Lupo, C, et al. Risk and indicators of condemnation of male turkey broilers in western France, February-July 2006. Preventive Veterinary Medicine 2010; 94: 240250.Google Scholar
15. Grist, A. Poultry Inspection, 2nd edn. Nottingham: Nottingham University Press, 2006, pp. 276.Google Scholar
16. Jordan, FTW. Avian tuberculosis. In: Jordan, FTW, ed. Poultry Diseases, 3rd edn. London: Baillère Tindall, 1990, pp. 6873.Google Scholar
17. Fallavena, LCB, et al. Diagnosis of skin lesions in condemned or downgraded carcasses – a microscopic and macroscopic study. Avian Pathology 2000; 29: 557562.Google Scholar
18. Ansong-Danquah, J. A survey of carcass condemnation at a poultry abattoir and its application to disease management. Canadian Veterinary Journal 1987; 28: 5356.Google Scholar
19. EFSA. Scientific opinion on the use of animal-based measures to assess welfare of broilers. EFSA Journal 2012; 10: 2774.Google Scholar
20. Welfare Quality. Welfare quality assessment protocol for poultry (broilers, laying hens). Lelystad, The Netherlands, 2009, 114 pp.Google Scholar
21. Gouveia, KG, Vaz-Pires, P, Martins da Costa, P. Welfare assment of broilers through examination of haematomas, foot-pad dermatitis, scratches and breast blisters at processing. Animal Welfare 2009; 18: 4348.Google Scholar
22. Allain, V, et al. Relations between different skin lesions measured at slaughterhouse in broiler chickens and between prevalence of these lesions and different rearing factors. British Poultry Science 2009; 50: 407417.Google Scholar
23. Ekstrand, C, et al. Prevalence and control of foot-pad dermatitis in broilers in Sweden. British Poultry Science 1998; 39: 318324.Google Scholar
24. Berg, C. Pododermatitis and hock burn in broiler chickens. In: Weeks, CA, Butterworth, A, eds. Measuring and Auditing Broiler Welfare. Wallingford: CABI, 2004, pp. 3750.Google Scholar
25. Kumor, LW, et al. Cellulitis in broiler chickens: epidemiological trends, meat hygiene, and possible human health implications. Avian Diseases 1998; 42: 285291.CrossRefGoogle ScholarPubMed
26. Olkowski, AA, et al. Cellulitis lesions in commercial turkeys identified during processing. Veterinary Record 1999; 145: 228229.Google Scholar
27. Saint-Hilaire, S, Sears, W. Trends in cellulitis condemnations in the Ontario chicken industry between April 1998 and April 2001. Avian Diseases 2003; 47: 537548.Google Scholar
28. Elfadil, AA, Vaillancourt, JP, Meek, AH. Farm management risk factors associated with cellulitis in broiler chickens in southern Ontario. Avian Diseases 1996; 40: 699706.Google Scholar
29. Hoinville, LJ, et al. Proposed terms and concepts for describing and evaluating animal-health surveillance systems. Preventive Veterinary Medicine 2013; 112: 112.Google Scholar
30. Salman, MD, Stärk, KDC, Zepeda, C. Quality assurance applied to animal disease surveillance systems. Revue Scientifique et Technique de l'Office International des Epizooties 2003; 22: 689.Google Scholar
31. Fisher, ME, Trampel, DW, Griffith, RW. Post mortem detection of acute septicemia in broilers. Avian Diseases 1998; 42: 452461.Google Scholar
32. Enoe, C, et al. The need for built-in validation of surveillance data so that changes in diagnostic performance of post-mortem meat inspection can be detected. Preventive Veterinary Medicine 2003; 57: 117125.Google Scholar
33. Bonde, M, et al. Evaluation of sensitivity and specificity of routine meat inspection of Danish slaughter pigs using latent class analysis. Preventive Veterinary Medicine 2010; 94: 163169.Google Scholar
34. Stärk, KDC, Nevel, A. Strengths, weaknesses, opportunities and threats of the pig health monitoring systems used in England. Veterinary Record 2009; 165: 461465.Google Scholar
35. Hathaway, SC, Richards, MS. Determination of the performance attributes of post-mortem meat inspection procedures. Preventive Veterinary Medicine 1993; 16: 119131.Google Scholar
36. Stärk, KDC, et al. Strengths and weaknesses of meat inspection as a contribution to animal health and welfare surveillance. Food Control 2014; 39: 154162.Google Scholar
37. COMISURV. External scientific report submitted to EFSA on the contribution of meat inspection to animal health surveillance in poultry, 2012, 131 pp.Google Scholar
38. Martin, PAJ, Cameron, AR, Greiner, M. Demonstrating freedom from disease using a complex data sources 1: a new methodology based on scenario trees. Preventive Veterinary Medicine 2007; 79: 7197.Google Scholar
39.Anon. Commission Decision of 19 October 2005 laying down biosecurity measures to reduce the risk of transmission of highly pathogenic avian influenza caused by Influenza virus A subtype H5N1 from birds living in the wild to poultry and other captive birds and providing for an early detection system in areas at particular risk. Official Journal of the European Union 2005; L 274: 105.Google Scholar
40.Anon. Commission Decision of 25 June 2010 on the implementation by Member States of surveillance programmes for avian inf luenza in poultry and wild birds (notified under document C(2010) 4190). Official Journal of the European Union 2010; L 166: 22.Google Scholar
41. Christensen, J, et al. A scenario tree model for the Canadian Notifiable Avian Influenza Surveillance System and its application to estimation of probability of freedom and sample size determination. Preventive Veterinary Medicine 2011; 99: 161175.Google Scholar
42. Alba, A, et al. Assessment of different surveillance systems for avian influenza in commercial poultry in Catalonia (North-Eastern Spain). Preventive Veterinary Medicine 2010; 97: 107118.Google Scholar
43. Bremner, AS. Post mortem condemnation returns from poultry slaughterhouses in England and Wales. Veterinary Record 1994; 135: 622623.Google Scholar
44. Haslam, SM, et al. Prevalence and factors associated with it, of birds dead on arrival at the slaughterhouse and other rejection conditions in broiler chickens. British Poultry Science 2008; 49: 685696.Google Scholar
45. Lupo, C, et al. Risk factors for sanitary condemnation in broiler chickens and their relative impact: application of an original multiblock approach. Epidemiology and Infection 2010; 138: 364375.Google Scholar
46. Lovland, A, Kaldhusdal, M. Liver lesions seen at slaughter as an indicator of necrotic enteritis in broiler flocks. FEMS Immunology and Medical Microbiology 1999; 24: 345351.Google Scholar
47. Mayes, FJ. The incidence of bruising in broiler flocks. British Poultry Science 1980; 21: 505–9.Google Scholar
48. Kyvsgaard, NC, et al. Temporal changes and risk factors for foo-pad dermatitis in Danish broilers. Poultry Science 2013; 92: 2632.Google Scholar
49. Lund, VP, et al. Pathological manifestations observed in dead-on-arrival broilers at a Danish abattoir. British Poultry Science 2013; 54: 430440.Google Scholar
50. van Veen, L, et al. Increased condemnation of broilers associated with Ornithobacterium rhinotracheale . Veterinary Record 2000; 147: 422423.Google Scholar
51. van Veen, L, et al. Diagnosis and incidence of Ornithobacterium rhinotracheale in commercial broiler chickens at slaughter. Veterinary Record 2005; 156: 315.Google Scholar
52. Januskeviciene, G, et al. Analysis of pathologic lesions in the livestock and poultry slaughtered in the meat establishments of Lithuania. Veterinarija ir Zootechnika 2010; 52: 3342.Google Scholar
53. Stoev, SD, et al. Mycotoxic nephropathy in Bulgarian pigs and chickens: complex etiology and similarity to Balkan Endemic Nephropathy. Food Additives and Contaminants 2009; 27: 7288.Google Scholar
54. Radkowski, M, Uradzinski, J, Szteyn, J. The occurrence of infectious and parasitic diseases in poultry slaughtered in the district of Olsztyn, Poland, 1986–91. Avian Diseases 1996; 40: 285289.Google Scholar
55. Olkowski, AA, Kumor, LW, Classen, HL. Changing epidemiology of ascites in broiler chickens. Canadian Journal of Animal Science 1996; 76: 135140.Google Scholar
56. Tessier, M, et al. Cellulitis in broiler chickens: a one-year retrospective study in four Québec abattoirs. Avian Diseases 2001; 45: 191194.Google Scholar
57. Bielby, M. A review of broiler chicken condemnations in Western Canada in 1998. In: Proceedings of the Forty-eighth Western Poultry Disease Conference. Vancouver, Canada, 1999, pp. 78.Google Scholar
58. Herenda, D, Jakel, O. Poultry abattoir survey of carcass condemnation for standard, vegetarian, and free range chickens. Canadian Veterinary Journal 1994; 35: 293296.Google Scholar
59. Hutchison, TWS, Riddel, C. A study of hepatic lesions in broiler chickens at processing plants in Saskatchewan. Canadian Veterinary Journal 1990; 31: 2025.Google Scholar
60. Mallia, JG, et al. Risk factors for abattoir condemnation of turkey carcasses due to cyanosis in Southern Ontario. Poultry Science 2000; 79: 831837.Google Scholar
61. Weinstock, D, et al. Histopathology and epidemiology of condemnations due to squamous cell carcinoma in broiler chickens in North Carolina. Avian Diseases 1995; 39: 676686.Google Scholar
62. Zimmerman, FC, et al. Downgrading of heavy broiler chicken carcasses due to myodegenration of the anterior latissimus dorsi: pathologic and epidemiologic studies. Avian Diseases 2012; 56: 418421.Google Scholar
63. Jacobsen, G, Flôres, ML. Ascitic condemnations in broilers slaughtered under federal inspection between 2002 and 2006 in Rio Grande do Sul, Brazil. Cienca Rural 2008; 38: 19661971.Google Scholar
64. d'Arc, Moretti L, et al. Time series evaluation of traumatic lesions and airsacculitis at one poultry abattoir in the state of Sao Paulo, Brazil (1996–2005). Preventive Veterinary Medicine 2010; 94: 23123–9.Google Scholar
65. Santana, AP, et al. Causes of condemnation of carcasses from poultry in slaughterhouses located in state of Goias, Brazil. Cienca Rural 2008; 38: 25872592.Google Scholar
66. Paschoal, EC, Otutumi, LK, Silveira, AP. Major reasons for condemnation in broiler slaughter in a slaughter house located in the northwest of Parana, Brazil. Arquivos de Ciencas Veterinarias e Zoologia 2013; 15: 9397.Google Scholar
67. Spanamberg, A, et al. Aspergillus fumigatus from normal and condemned carcasses with airsacculitis in commercial poultry. Pesquisa Veterinaria Brasileira 2013; 33: 10711075.Google Scholar
68. Aboulela, MA. CAV and broiler downgrading. Poultry International 1998, pp. 3031.Google Scholar
69. Ansari-Lari, M, Rezagholi, M. Poultry abattoir survey of carcass condemnations in Fars province, southern Iran. Preventive Veterinary Medicine 2007; 79: 287293.Google Scholar
70. Sekizaki, T, et al. Endocarditis in chickens caused by subclinical infection of Streptococcus gallolyticus subsp. gallolyticus. Avian Diseases 2008; 52: 183186.Google Scholar
Figure 0

Table 1. Examples of studies using Meat Inspection (MI) for monitoring health and welfare in poultry in Europe, North America, South America, Middle East and Asia. Classification of the studies according to their objectives: ‘case report’ (description of a new condition), ‘prevalence’ (assessment of condition prevalence and its temporal evolution), ‘aetiology’ (identification of the aetiology of a condition) and ‘risk factors’ (identification of factors associated with the occurrence of a condition)

Figure 1

Table 2. Qualitative assessment of Meat Inspection (MI) as a surveillance component for health and welfare surveillance in poultry in the European Union (adapted from Salman et al. [30])

Figure 2

Table 3. Strength-Weakness-Opportunity-Threat (SWOT) analysis of Meat Inspection (MI) as a surveillance system of animal health and welfare surveillance

Figure 3

Fig. 1. Flow diagram of the scenario tree model, with the arrows indicating the order that each step occurs, i.e. node of the tree is calculated. AMI, Ante-mortem inspection; PMI, post-mortem inspection.

Figure 4

Table 4. Probabilities of case detection (mode) of ante- and post-mortem inspection procedures at individual bird level (5% and 95% percentiles) for 20 diseases and conditions

Figure 5

Table 5. Estimated proportion of turkeys and turkey batches detected as true positives for avian influenza by different surveillance system components

Figure 6

Table 6. Detection fraction at batch level (10 000 birds) of selected endemic diseases/conditions by abattoir inspection and clinical suspicion and comparative detection performance with an assumed coverage of 100%