Hostname: page-component-586b7cd67f-tf8b9 Total loading time: 0 Render date: 2024-11-24T12:35:36.389Z Has data issue: false hasContentIssue false

Prevalence of lameness and claw lesions during different stages in the reproductive cycle of sows and the impact on reproduction results

Published online by Cambridge University Press:  14 March 2013

L. M. Pluym
Affiliation:
Technology and Food Sciences Unit, Institute of Agricultural and Fisheries Research, Burgemeester Van Gansberghelaan 115 bus 1, 9820 Merelbeke, Belgium Department of Reproduction, Obstetrics and Herd Health, Ghent University, Salisburylaan 133, 9820 Merelbeke, Belgium
A. Van Nuffel
Affiliation:
Technology and Food Sciences Unit, Institute of Agricultural and Fisheries Research, Burgemeester Van Gansberghelaan 115 bus 1, 9820 Merelbeke, Belgium
S. Van Weyenberg
Affiliation:
Technology and Food Sciences Unit, Institute of Agricultural and Fisheries Research, Burgemeester Van Gansberghelaan 115 bus 1, 9820 Merelbeke, Belgium
D. Maes*
Affiliation:
Department of Reproduction, Obstetrics and Herd Health, Ghent University, Salisburylaan 133, 9820 Merelbeke, Belgium
*

Abstract

Lameness in sows is an emerging disease condition with major effects on animal welfare and economics. Yet the direct impact on reproduction results remains unclear. The present field study investigated the impact of lameness and claw lesions throughout the reproductive cycle on (re)production results of sows. In five farms, a total of 491 group-housed sows were followed up for a period of one reproductive cycle. Sows were assessed for lameness every time they were moved to another area in the farm. Claw lesions were scored at the beginning and at the end of the cycle. Reproduction results included the number of live-born piglets, stillborn piglets, mummified fetuses and crushed piglets, weaning-to-oestrus interval and the presence of sows not showing oestrus post weaning, returning to service and aborting. Sows that left the group were recorded and the reason was noted. A mean prevalence of lameness of 5.9% was found, although it depended on the time in the productive cycle. The highest percentage of lame sows (8.1%) was found when sows were moved from the post-weaning to the gestation stable. No significant associations were found between lameness and reproduction parameters with the exception of the effect on mummified foetuses. Wall cracks, white line lesions, heel lesions and skin lesions did have an effect on farrowing performance. Of all sows, 22% left the group throughout the study, and almost half of these sows were removed from the farm. Lameness was the second most important reason for culling. Sows culled because of lameness were significantly younger compared with sows culled for other reasons (parity: 2.6 ± 1.3 v. 4.0 ± 1.8). In conclusion, the present results indicate that lameness mainly affects farm productivity indirectly through its effect on sow longevity, whereas claw lesions directly affect some reproductive parameters. The high percentage of lame sows in the insemination stable indicate that risk factor studies should not only focus on the gestation stable, but also on housing conditions in the insemination stable.

Type
Behaviour, welfare and health
Creative Commons
Creative Common License - CCCreative Common License - BYCreative Common License - NCCreative Common License - SA
The online version of this article is published within an Open Access environment subject to the conditions of the Creative Commons Attribution-NonCommercial-ShareAlike licence . The written permission of Cambridge University Press must be obtained for commercial re-use
Copyright
Copyright © The Animal Consortium 2013 The online version of this article is published within an Open Access environment subject to the conditions of the Creative Commons Attribution-NonCommercial-ShareAlike licence <http://creativecommons.org/licenses/by-nc-sa/2.5/>. The written permission of Cambridge University Press must be obtained for commercial re-use.

Implications

Knowledge on the economic impact of claw lesions and lameness helps to understand how both the diseases influence economic losses, and indicates how these problems should best be addressed. The fact that the prevalence of lameness varies throughout the reproductive cycle and peaks after sows were housed in the insemination stable is crucial for risk factor analysis. Furthermore, it implicates that focus on housing in the insemination stable is important to improve the prevention strategy.

Introduction

Lameness is a growing concern in swine breeding herds. Owing to the pain, suffering and limited freedom of movement, lameness is recognized as an important welfare concern (Whay et al., Reference Whay, Main, Green and Webster2003). Nowadays, the disease condition is implemented in the Welfare Quality® Assessment Protocol for pigs (Welfare Quality®, 2009).

In addition to the impaired welfare, lameness is allied to financial loss estimated at €37 per lame sow in Germany (Grandjot, Reference Grandjot2007), $180 per lame sow in the United States (Deen et al., Reference Deen, Anil, Anil and Baidoo2008) and in a Dutch study, €20 to 30 per sow present in the farm (Schuttert, Reference Schuttert2008). Economic losses can be attributed to increased work load, higher veterinary costs because of treatment or euthanasia, higher risk for total or partial condemnation resulting in less slaughter revenue and to an impact on reproduction (Rowles, Reference Rowles2001; Schuttert, Reference Schuttert2008). The impact on reproduction can be divided into a direct and an indirect effect. Literature on the indirect effect of lameness on reproduction is more widespread and much more consistent than the direct impact on reproduction.

Indirectly, lameness may affect reproduction of sows by influencing sows’ longevity, behaviour and feed intake. Lameness is the most important reason for euthanasia and the second most important reason for involuntary culling (Engblom et al., Reference Engblom, Lundeheim, Dalin and Andersson2007; Jensen et al., Reference Jensen, Bonde, Kongsted, Toft and Sørensen2010), leading to a detrimental impact on sow longevity. According to Bonde et al., (Reference Bonde, Rousing, Badsberg and Sørensen2004), lameness leads to uncontrolled lying-down behaviour and, as a consequence, it may augment the risk of crushing piglets. The higher level of acute-phase proteins in lame sows indicates the presence of inflammatory processes (Heinonen et al., Reference Heinonen, Oravainen, Orro, Seppä-Lassila, Ala-Kurikka, Virolainen, Tast and Peltoniemi2006). Cytokines released by the inflammatory processes predispose to anorexia and lethargic behaviour (Johnson, Reference Johnson1997). In addition, Fitzgerald et al., (Reference Fitzgerald, Stalder, Karriker, Sadler, Hill, Kaisand and Johnson2012) reported a negative effect of overgrown toes on feed consumption during lactation. Early culling of sows, reduced feed intake and impaired locomotion indirectly decrease the mean number of litters per sow per year and the mean number of weaned pigs per sow per year, increasing the cost per weaned piglet.

However, the direct effect of lameness on reproduction (i.e. direct improvement or deterioration of the breeding or farrowing performance of a sow), is less clear. Several studies did not find any effect (Kroneman et al., Reference Kroneman, Vellenga, van der Wilt and Vermeer1993; Andersen and Bøe, Reference Andersen and Bøe1999; Heinonen et al., Reference Heinonen, Oravainen, Orro, Seppä-Lassila, Ala-Kurikka, Virolainen, Tast and Peltoniemi2006; Willgert, Reference Willgert2011), whereas other studies described a negative relationship between lameness and farrowing performance (Grandjot, Reference Grandjot2007; Anil et al., Reference Anil, Anil and Deen2009). Moreover, comparison between these studies is difficult as different methods and different stages in the reproductive cycle were used to assess lameness. As sows can recover over time, it may be recommended to assess lameness in the same sows at several times. In addition, knowledge on the stage in the reproductive cycle at which lameness is most prevalent may have a key value regarding risk factor analysis.

In breeding herds, sows are commonly housed in three main areas: the insemination stable (shortly after weaning), the gestation stable and the farrowing crates. Each of these areas is related to a different physiological status of the sow and is characterized by its own specific floor, feeding strategy, environment and management. Several studies already referred to floor characteristics (Newton et al., Reference Newton, Booram, Hale and Mullinix1980; Mouttotou et al., Reference Mouttotou, Hatchell and Green1999) and feed (Simmins and Brooks, Reference Simmins and Brooks1988) as important risk factors for claw lesions and lameness. When sows are moved to a new area within the farm, the possible risk factors for development of lameness to which sows may be exposed will also change.

The aim of the present study was to evaluate the short-term effect of lameness and claw lesions on (re)production at the three main stages of the reproductive cycle in sows. In addition, the prevalence of lameness and claw lesions was investigated at each of these three stages.

Material and methods

Animals and housing

A total of 491 sows from five randomly selected farms were included in the study. General information about every farm is given in Table 1. All farms had at least 750 sows and all sows were housed in groups during gestation. On all farms, the gestation stable was provided with a partly slatted, concrete floor without bedding material. Farms 1 to 4 used free access stalls. On farm 5, sows were housed in small groups of 15 sows per pen and were fed by use of trough feeding. Space per animal during gestation ranged between 2.0 and 2.6 m2. At the insemination unit, sows were housed individually with solid concrete flooring in the front half and concrete slats in the rear half. Only on the farm 5 metal slats were used in the rear half. The width of the concrete slats varied between 8 and 11 cm whereas the metal slats measured 1 cm. Slots of the floors on all farms did not exceed 2 cm. Farrowing stalls contained cast iron (partly), slatted flooring without bedding. During lactation, sows were provided feed and water ad libitum. As farm 2 had recently started with new sows, all sows had farrowed only once at the beginning of the study.

Table 1 Descriptive data of the farms (n = 5) and the investigated group of sows on each farm in the study

FAS = free access stalls; na = data not available.

Part of the sows left the group during the study due to culling, euthanasia, death, anoestrus, rebreeding or abortion. The mean parity of the sows that left the group as well as of the sows that remained in the group is also given.

Measurements

Within each farm, one randomly selected group of sows was followed up for a period of one reproductive cycle (from weaning to weaning). Every group was investigated five times, that is two claw lesion scorings and three lameness assessments, over a period of 5 months (Figure 1). Visual lameness assessment was performed on the day the sows were moved from one stage on the farm to another (L1, L2 and L3) and was based on the Welfare Quality® Protocol. In this protocol, a lame sow is defined as a sow unable to use one or more limbs in a normal manner varying in severity from reduced ability to bear weight, to total recumbancy. However, in the present study, only distinction was made between lame and healthy sows. Claw lesion scoring of sows was carried out twice in the farrowing stable: 1 week before the sows were weaned (C1) and 1 week after farrowing (C2) (Figure 1). Seven claw parameters were scored: length of toes, length of dew claws, wall cracks, heel cracks and/or overgrowth, skin lesions above the claw, heel–sole cracks and white line cracks. The first five parameters were based on the Dutch scoring method ‘Nederlandse Zeugenklauwencheck’ (Hoofs, Reference Hoofs2006). The last two parameters were scored following the Zinpro®Feet First method (Feet First®Team, 2010). Each of the four claws of the hind legs were scored from one to four, with score 1 meaning no lesion and score 4 meaning a severe lesion. The sum of the score of the four claws was made and was called the ‘total score’ (minimum 4 to maximum 16). However, when performing statistical analysis, total score was included as a dichotomous variable. This means that sows without lesions on any of the four claws (total score = 4) were coded 0 and sows with a total score of 5 to 16 were coded 1. By summing the seven ‘total scores’, a ‘global score’ was obtained for each sow (minimum 28 to maximum 112). For the data and statistical analyses, global scores were regarded as continuous variables.

Figure 1 Measurements during the reproductive cycle of the sows: Lameness assessment was performed when sows were moved between different stables (L1 to L3). Claw lesion scoring was performed in the farrowing stable: 1 week before weaning and 1 week after farrowing (C1 and C2). Reproduction data of one period were considered (breeding performance, farrowing performance and crushed piglets). C1, C2 = claw lesion score; L1, L2, L3 = lameness assessment 1, 2 and 3.

Parity of sows was categorized into four groups: 1, 2, 3 to 5 and ⩾6 parity. Reproduction results in this study are defined as a combination of the farrowing performance, crushed piglets and the breeding performance. Information on farrowing performance and crushed piglets that was collected for the investigated cycle included the number of piglets born alive (continuous variable) and the absence or presence of stillborn piglets, mummified foetuses and crushed piglets (dichotomous variables). The breeding performance of sows included ‘showing oestrus post-weaning’, ‘weaning-to-oestrus interval’, ‘returning to service’ and ‘abortion’ (defined as expulsion of foetuses between day 35 and day 108 of gestation). The weaning-to-oestrus interval was regarded as a continuous variable, the other three as dichotomous variables. Coming into oestrus within 10 days after weaning, positive pregnancy diagnosis by ultrasound scanning 23 to 35 days after breeding and absence of abortion were coded as normal (0).

Sows that left the group during the study were recorded, as well as the time and the reason (not coming in oestrus, returning to service, abortion, death, euthanasia or culling). As it is essentially different, distinction was made between sows that left the group because they were removed from the farm (sows removed from the farm) and sows that left the group but that remained on the farm (sows removed from the group). The reasons for removing sows from the farm were culling, euthanasia or death. The reason why sows left the group but remained in the farm was because they did not show oestrus, they returned to service or they aborted.

An overview of the reproduction results across all farms is given in Table 2.

Table 2 Overview of the farrowing and breeding performance of the sows in the study

Descriptive data on the number of piglets born alive, stillborn piglets, mummified foetuses and crushed piglets over all 381 sows as well as descriptive data on breeding performance including the mean weaning-to-oestrus interval and the mean number and percentage of sows that did not show oestrus, did return to service or aborted during the study.

Statistical analysis

Normality of continuous variables was evaluated. Linear and logistic regression models were built with farrowing and breeding-related variables as dependent variables. To account for the clustering of sow in the farm, a fixed farm effect was included. In addition, total and global claw lesion scores, as well as lameness and parity, were included as fixed effects. A stepwise forward model-building procedure was followed, and all factors with a P-value <0.05 were retained in the final multivariable model.

Descriptive statistics were used to illustrate the prevalence of claw lesions and lameness throughout the productive cycle. To evaluate whether parity and global score differ between healthy and lame sows (0/1), between sows that were (1) or were not (0) removed from the farm, and between sows removed because of lameness (1) or because of other reasons (0), univariable linear regressions, with either parity or global score as dependent variable and farm as fixed effect, were performed. To evaluate the difference in global score between the first and the second claw lesion scoring, mixed model linear regression was performed, with global score as dependent variable, sow as random effect, to correct for repeated measurements, and time of claw lesion scoring, farm and interaction time × farm as fixed effects.

All statistical analyses were performed using IBM SPSS Statistics 19 (IBM, New York, USA).

To analyse the effect of the three measuring periods (L1, L2 and L3) on lameness, a multilevel logistic regression model was fit using MLwiN 2.02 (Centre for Multilevel Modeling, Bristol, UK). Farm (1 to 5), measuring period and the interaction farm × measuring period were included as fixed effects.

Results

Impact on (re)production results

After stepwise forward model building, significant associations were found between the independent variables (parity, lameness, claw score and farm) and the dependent variables (stillborn piglets, mummified foetuses, crushed piglets and number of live born piglets) (Table 3). In the final model, no significant associations between risk factors and breeding performance (showing oestrus post weaning, weaning-to-oestrus interval, returning to service and abortion) were found. However, several claw lesions were related to farrowing performance. The presence of skin lesions above the claw (P = 0.021) and white line lesions (P = 0.036) significantly increased the odds of stillborn piglets. Heel lesions were significantly associated with the presence of crushed piglets (P = 0.017). The odds of mummified foetuses increased when wall cracks were present (P = 0.044). An influence of lameness could only be found for the presence of mummified foetuses. The odds of having mummified foetuses were twice as high in lame sows compared with healthy sows. A significant farm effect was found for all of the farrowing results, whereas parity was significantly associated with the presence of stillborn piglets and crushed piglets (Table 3).

Table 3 Final multivariable logistic regression models related to the risk factors for farrowing performance and crushed piglets with farm, parity, claw score and lameness as independent variables and presence of stillborn piglets, mummified foetuses and crushed piglets as dependent variables

Regression analyses were based on the results of 306 sows.

aTotal claw score for white line lesions.

bTotal claw score for skin lesions above the claw.

cTotal claw score for wall cracks.

dTotal claw score for heel cracks and overgrowth. The number behind the total score refers to the first time (at weaning) or second time (at farrowing) claw lesion scoring was performed.

eAbsence (0) or presence (1) of stillborn, mummified and crushed piglets, respectively.

b, regression coefficient.

Prevalence of claw lesions

The percentage of sows with and without lesions for each of the seven claw parameters that were scored the first and second time claw lesion scoring was performed, are represented in Figure 2. Heel cracks were found to be the most frequent lesions (96% sows with lesions) whereas skin lesions above the claw were only occasionally found (8% of sows with lesions). No significant difference in global score, the sum of seven total scores, was present between the sows that remained in the group and the sows that left the group during the study. In general, the mean global score slightly improved from first (mean (s.d.) score of 35.8 (3.9)) to second time (mean (s.d.) score of 34.9 (3.2)). However, a significant farm × time interaction (P = 0.012) was found. The change between the first and second global score was found to be significant only at farms 1 and 4.

Figure 2 Percentage of sows (total of 381) with and without lesions for each of the seven claw parameters that were scored at the first (1) and second (2) time claw lesion scoring was carried out. 1, performed at the end of the first lactation period, at the beginning of the study; 2, performed 5 days after parturition in the second lactation period, at the end of the study.

Prevalence of lameness

In total, 106 sows (21.6%) left the group during the study. Of these, 54 sows (51.0%) were removed from the group with returning to service as the most important reason. The remaining 52 sows (49.0%) were removed from the farm because of culling, euthanasia or death. Udder health problems (33%) and feet and leg problems (15%) were the most important reasons for culling. Sows that were removed from the farm had a mean parity of 4.0 ± 1.8, whereas sows specifically culled because of feet and leg problems had a mean parity of 2.6 ± 1.3.

Figure 3 shows the percentage of sows that were scored lame at the three visual lameness assessments (L1-L2-L3). The mean percentage of lame sows for all farms was 5.5 ± 3.3%, 8.1 ± 6.1% and 4.1 ± 4.4% at L1, L2 and L3, respectively. The difference between L1, L2 and L3 was found to be significant (P = 0.027) and the prevalence of lameness significantly varied according to the farm (P = 0.002). The interaction between farm and measuring period was not significant. On every farm, the percentage of lame sows peaked at the moment of the second lameness investigation, that is, when sows were moved from the insemination stable to the gestation stable. At L1, 27 sows were assessed to be lame. Of these, nine sows left the group before L2 could be performed. At L2, a total of 32 lame sows were found. Only two sows that were lame at L1 were still lame at L2 and four sows that were lame at L2 were also lame at L3. There was no significant difference in parity between sows that were lame (mean parity of 2.6 ± 1.7) and sows that were not lame (mean parity of 2.5 ± 1.7).

Figure 3 Percentage of sows that were lame at the three visual lameness assessments (L1 to L3) for each farm (F1 to F5).

Discussion

Direct impact

On the basis of the models, some claw lesions seem to have a direct impact on farrowing performance of sows. An effect of claw lesions on reproductive performance was also reported by De Pita (Reference De Pita2010), Anil (Reference Anil2011) and Fitzgerald et al. (Reference Fitzgerald, Stalder, Karriker, Sadler, Hill, Kaisand and Johnson2012) but could not be shown by Enokida et al. (Reference Enokida, Sasaki, Hoshino, Saito and Koketsu2011). In the present study, white line lesions and skin lesions above the claw increased the risk for stillborn piglets. Both skin lesions and white line lesions may facilitate entry of bacteria causing infection, pain and clinical lameness. An association between white line lesions and lameness in breeding sows was described by Anil et al. (Reference Anil, Anil, Deen, Baidoo and Walker2007). De Pita (Reference De Pita2010) reported a positive association between white line lesions and the likelihood of having ⩽10 piglets born alive. In the same study, the likelihood of having ⩽10 piglets born alive was positively associated with the number of stillborn piglets. The reason why sows with wall cracks have lower odds of having mummified foetuses remains unknown.

Contrary to claw lesions, a clear direct impact of lameness on breeding and farrowing performance could not be shown with the exception of the effect on mummified foetuses. Lameness is a clinical sign that shows that movement is painful. The higher serum concentrations of acute-phase proteins in lame sows reported by Heinonen et al. (Reference Heinonen, Oravainen, Orro, Seppä-Lassila, Ala-Kurikka, Virolainen, Tast and Peltoniemi2006) indicate the presence of inflammatory processes. Pain and inflammation may cause reduction in feed intake and consequently may lead to a poor body condition of the sow. Poor body condition has been associated with the presence of mummified foetuses in sows (Knauer et al., Reference Knauer, Stalder, Karriker, Johnson and Layman2006).

Apart from the effect on mummified foetuses, no effect of lameness on reproduction was found in the present study. This is in contrast with the lower number of piglets born alive and higher piglet losses before weaning reported by Grandjot (Reference Grandjot2007) and Anil et al. (Reference Anil, Anil and Deen2009). The absence of a significant association between lameness and reproductive performance may be explained by the fact that reproduction results may strongly differ between individual sows. Therefore, it can be suggested to evaluate the impact on reproduction in longitudinal studies covering several reproductive cycles and using a sow as her own reference. However, in this study, parity and farm, as indicators for breed effect, were already taken into account when performing linear and logistic regression.

Indirect impact

In addition to the direct impact, lameness and claw lesions are assumed to have an indirect impact on reproduction results. Indeed, a relationship with the risk of removal from the farm was found as well as a significant association between heel lesions and crushed piglets.

With a prevalence of 15%, feet- and leg problems appeared to be the second most important reason for sow removal in this study. Moreover, sows removed from the farm because of feet and leg problems were significantly younger compared with sows removed because of other reasons. The finding that feet and leg problems are important reasons of early culling is in agreement with the results of other studies (Stalder et al., Reference Stalder, Lacy, Cross and Conatser2003; Engblom et al., Reference Engblom, Lundeheim, Dalin and Andersson2007; Jensen et al., Reference Jensen, Bonde, Kongsted, Toft and Sørensen2010). Sows reach peak production between the third and sixth parity. Hence, removal of sows at a mean parity of 2.6 implies that part of the sows did not reach their most productive parities, nor repaid their investment costs yet (Ritter et al., Reference Ritter, Xue, Dial, Morrison and Marsh1999; Stalder et al., Reference Stalder, Lacy, Cross and Conatser2003; Anil et al., Reference Anil, Anil and Deen2009). A higher removal rate also increases replacement costs and the frequency of adding new gilts, which in turn implicates a higher health risk to the animals currently in the farm.

In this study, a negative association was found between the presence of heel lesions and presence of crushed piglets. Heel lesions are very common among sows. The high percentage of sows with heel lesions (96%) in this study is in agreement with the results of previous studies (Gjein and Larssen, Reference Gjein and Larssen1995; Anil et al., Reference Anil, Anil, Deen, Baidoo and Walker2007; Pluym et al., Reference Pluym, Van Nuffel, Dewulf, Cools, Vangroenweghe, Van Hoorebeke and Maes2011). Only a few sows did not have any heel lesion. Owing to the low number of sows without lesions, the association found between heel lesions and crushed piglets may not be an effect but just coincidence.

Prevalence of claw lesions and lameness

To be able to perform thorough risk factor analysis, and to start prevention at the right moment, knowledge on the changes in the prevalence of lameness and claw lesions throughout the reproductive cycle is important. The mean global score in general remained unchanged but significantly improved from first to second claw lesion scoring on farms 1 and 4. Trimming of long toes and healing of lesions may have contributed to this improvement. The high prevalence of sows with heel cracks and overgrowth was also observed in other studies (Gjein and Larssen, Reference Gjein and Larssen1995; Anil et al., Reference Anil, Anil, Deen, Baidoo and Walker2007; Pluym et al., Reference Pluym, Van Nuffel, Dewulf, Cools, Vangroenweghe, Van Hoorebeke and Maes2011). The mean prevalence of lameness namely 5.6%, 8.7% and 5.1% at L1, L2 and L3, respectively, were slightly lower compared with the prevalence of 9.7% that was found in an earlier study conducted on Belgian farms (Pluym et al., Reference Pluym, Van Nuffel, Dewulf, Cools, Vangroenweghe, Van Hoorebeke and Maes2011). High differences between farms, as seen in other studies (Heinonen et al., Reference Heinonen, Oravainen, Orro, Seppä-Lassila, Ala-Kurikka, Virolainen, Tast and Peltoniemi2006; Pluym et al., Reference Pluym, Van Nuffel, Dewulf, Cools, Vangroenweghe, Van Hoorebeke and Maes2011), were also noticed in this study. Group housing is mentioned as an important risk factor for lameness (Anil et al., Reference Anil, Anil, Deen, Baidoo and Wheaton2005; Chapinal et al., Reference Chapinal, Ruiz de la Torre, Cerisuelo, Gasa, Baucells, Coma, Vidal and Manteca2010). Notwithstanding, in this study, the prevalence of lameness was lowest at the end of the gestation period (L3) and highest at the moment the sows were moved from the insemination stable to the gestation stable (L2). On farm 2, lameness assessment could not be done when sows were moved from the insemination to the gestation stable, and therefore had to be done 2 weeks after the sows were introduced in group housing (stable groups). However, even without this farm, the prevalence remained highest at L2 (data not shown). Group housing probably can influence the development of lameness, especially shortly after introduction when sows fight to establish a dominance hierarchy. When this equilibrium is found, sows may have the time to heal from their injuries (Arey, Reference Arey1998). Nevertheless, results of this study suggest that even housing in the insemination stable may have an impact on the development of lameness. The increase in prevalence at L2 is caused by a higher number of lame sows and not by a lower number of total sows owing to the sows leaving the group between L1 and L2. In the insemination stable, sows were housed in conventional stalls. Owing to immobility, muscle conformation and bone strength can deteriorate (Marchant and Broom, Reference Marchant and Broom1994). However, in the present study, sows were housed in stalls for at most 5 weeks, whereas impact of restricted mobility on the development of muscle and bone strength (Marchant and Broom, Reference Marchant and Broom1994), as well as on lameness (Karlen et al., Reference Karlen, Hemsworth, Gonyou, Fabrega, Strom and Smits2007), could only be shown after housing sows in stalls during almost the entire gestation period.

In addition to the differences between L1, L2 and L3, the prevalence of lameness significantly varied between farms. Differences in management (e.g. handling of animals, moving the sows at the time of oestrus detection) might explain the variation between farms. These results indicate that the prevalence of lameness differs throughout the reproductive cycle and that changes vary according to the farm. This substantiates our suggestion that lameness should be assessed several times during the reproductive cycle.

Conclusion

A direct effect of certain claw lesions on the farrowing performance of sows was shown, whereas for lameness a clear indirect impact on (re)production results was found. The prevalence of lameness differed between farms and varied throughout the reproductive cycle. Housing in the insemination stable seems to induce more lameness than housing in the gestation stable in the farms studied. Therefore, further investigation on risk factors, especially related to the insemination stable and introduction of sows in group housing is needed.

Acknowledgements

This research was granted by ‘The Institute for Innovation through Science and Technology (IWT) Flanders, Belgium’ (Innovation study SB-091420). The authors are grateful to the farmers for their willingness to cooperate in this study.

References

Andersen, IL, Bøe, KE 1999. Straw bedding or concrete floor for loose-housed pregnant sows: consequences for aggression, production and physical health. Acta Agriculturae Scandinavica, Section A – Animal Science 49, 190195.Google Scholar
Anil, SS 2011. Epidemiology of lameness in breeding female pigs. PhD University of Minnesota.Google Scholar
Anil, SS, Anil, L, Deen, J 2009. Effect of lameness on sow longevity. Journal of the American Veterinary Medical Association 235, 734738.CrossRefGoogle ScholarPubMed
Anil, L, Anil, SS, Deen, J, Baidoo, SK, Wheaton, JE 2005. Evaluation of well-being, productivity and longevity of pregnant sows housed in groups in pens with an electronic sow feeder or separately in gestation stalls. American Journal of Veterinary Research 66, 16301638.Google Scholar
Anil, SS, Anil, L, Deen, J, Baidoo, SK, Walker, RD 2007. Factors associated with claw lesions in gestating sows. Journal of Swine Health and Production 15, 7883.Google Scholar
Arey, DS 1998. Time course for the formation and disruption of social organization in group-housed sows. Applied Animal Behaviour Science 62, 199207.Google Scholar
Bonde, M, Rousing, T, Badsberg, JH, Sørensen, JT 2004. Associations between lying-down behaviour problems and body condition, limb disorders and skin lesions of lactating sows housed in farrowing crates in commercial sow farms. Livestock Production Science 87, 179187.Google Scholar
Chapinal, N, Ruiz de la Torre, JL, Cerisuelo, A, Gasa, J, Baucells, MD, Coma, J, Vidal, A, Manteca, X 2010. Evaluation of welfare and productivity in pregnant sows kept in stalls or in 2 different group housing systems. Journal of Veterinary Behavior 5, 8293.CrossRefGoogle Scholar
Deen, J, Anil, SS, Anil, L, Baidoo, S. 2008. Lameness overview and awareness: implications for welfare, housing, performance and economics. FeetFirstTM Symposium on Sow Lameness, Asten/Sterksel, The Netherlands, 4pp.Google Scholar
De Pita, ADS. 2010. Sow lameness and claw lesions evaluation. Master Thesis, University of Minnesota.Google Scholar
Engblom, L, Lundeheim, N, Dalin, AM, Andersson, K 2007. Sow removal in Swedish commercial farms. Livestock Science 106, 7686.Google Scholar
Enokida, M, Sasaki, Y, Hoshino, Y, Saito, H, Koketsu, Y 2011. Claw lesions in lactating sows on commercial farms were associated with postural behavior but not with suboptimal reproductive performance or culling risk. Livestock Science 136, 256261.Google Scholar
Feet First® Team 2010. Feet First® swine claw lesion identification. Retrieved December 23, 2010, from http://www.zinpro.com/lameness/swine/lesion-identification.Google Scholar
Fitzgerald, RF, Stalder, KJ, Karriker, LA, Sadler, LJ, Hill, HT, Kaisand, J, Johnson, AK 2012. The effect of hoof abnormalities on sow behavior and performance. Livestock Science 145, 230238.Google Scholar
Gjein, H, Larssen, RB 1995. Housing of pregnant sows in loose and confined systems – a field study. 2. Claw lesions: morphology, prevalence, location and relation to age. Acta Veterinaria Scandinavica 36, 433442.CrossRefGoogle ScholarPubMed
Grandjot, G 2007. Claw problems cost money SUS-Schweinezucht und Schweinemast Landwirtschaftsverlag GmbH. Munster-Hiltrup, Germany 5, 2831.Google Scholar
Heinonen, M, Oravainen, J, Orro, T, Seppä-Lassila, L, Ala-Kurikka, E, Virolainen, J, Tast, A, Peltoniemi, OAT 2006. Lameness and fertility of sows and gilts in randomly selected loose-housed farms in Finland. The Veterinary Record 159, 383387.Google Scholar
Hoofs, AIJ, Netwerk ‘perfecte zeugenklauw’ 2006. De Nederlandse Zeugenklauwencheck (in Dutch). Retrieved December 23, 2010, from http://www.verantwoordeveehouderij.nl/netwerken/enquete/zeugenklauwencheck/Klauwencheck.pdf.Google Scholar
Jensen, TB, Bonde, MK, Kongsted, AG, Toft, N, Sørensen, JT 2010. The interrelationships between clinical signs and their effect on involuntary culling among pregnant sows in group-housing systems. Animal 4, 19221928.Google Scholar
Johnson, RW 1997. Inhibition of growth by pro-inflammatory cytokines: an integrated view. Journal of Animal Science 75, 12441255.CrossRefGoogle ScholarPubMed
Karlen, GAM, Hemsworth, PH, Gonyou, HW, Fabrega, E, Strom, AD, Smits, RJ 2007. The welfare of gestating sows in conventional stalls and large groups on deep litter. Applied Animal Behaviour Science 105, 87101.Google Scholar
Knauer, MT, Stalder, KJ, Karriker, L, Johnson, C, Layman, L. 2006. Factors influencing sow culling. Retrieved November 2, 2012, from http://www.nsif.com/Conferences/2006/pdf/FactorsInfluencingSowCulling.pdf.Google Scholar
Kroneman, A, Vellenga, L, van der Wilt, FJ, Vermeer, HM 1993. Field research on veterinary problems in group-housed sows – a survey of lameness. Journal of Veterinary Medicine A 40, 704712.CrossRefGoogle ScholarPubMed
Marchant, JN, Broom, DM 1994. Effects of housing system on movement and leg strength in sows. Applied Animal Behaviour Science 41, 275276.Google Scholar
Mouttotou, N, Hatchell, FM, Green, LE 1999. Foot lesions in finishing pigs and their associations with the type of floor. The Veterinary Record 144, 629632.Google Scholar
Newton, GL, Booram, CV, Hale, OM, Mullinix, G Jr 1980. Effects of four types of floor slats on certain feet characteristics and performance of swine. Journal of Animal Science 50, 720.CrossRefGoogle Scholar
Pluym, L, Van Nuffel, A, Dewulf, J, Cools, A, Vangroenweghe, F, Van Hoorebeke, S, Maes, D 2011. Prevalence and risk factors of claw lesions and lameness in pregnant sows in two types of group housing. Veterinarni Medicina 56, 101109.Google Scholar
Ritter, LA, Xue, J, Dial, GD, Morrison, RB, Marsh, WE 1999. Prevalence of lesions and body condition scores among female swine at slaughter. Journal of the American Veterinary Medical Association 214, 525528.CrossRefGoogle ScholarPubMed
Rowles, C 2001. Sow lameness. Journal of Swine Health and Production 9, 130131.Google Scholar
Simmins, PH, Brooks, PH 1988. Supplementary biotin for sows: effect on claw integrity. Veterinary Record 122, 431435.CrossRefGoogle ScholarPubMed
Schuttert, M, 2008. The economical impact of lameness in sows. FeetFirstTM Symposium on Sow Lameness, Asten/Sterksel, The Netherlands, 4pp.Google Scholar
Stalder, KJ, Lacy, CR, Cross, TL, Conatser, GE 2003. Financial impact of average parity of culled females in a breed-to-wean swine operation using replacement gilt net present value analysis. Journal of Swine Health and Production 11, 6974.Google Scholar
Welfare Quality ® 2009. Welfare Quality® assessment protocol for pigs (sows and piglets, growing and finishing pigs). Welfare Quality® Consortium, Lelystad, The Netherlands.Google Scholar
Whay, HR, Main, DCJ, Green, LE, Webster, AJF 2003. Animal-based measures for the assessment of welfare state of dairy cattle, pigs and laying hens: consensus of expert opinion. Animal Welfare 12, 205217.Google Scholar
Willgert, K, 2011. The economic and welfare impact of lameness in sows in England. Retrieved January 10, 2012, from http://www.fao.org/fileadmin/user_upload/animalwelfare/TheeconomicandwelfareimpactoflamenessinsowsinEngland.pdf.Google Scholar
Figure 0

Table 1 Descriptive data of the farms (n = 5) and the investigated group of sows on each farm in the study

Figure 1

Figure 1 Measurements during the reproductive cycle of the sows: Lameness assessment was performed when sows were moved between different stables (L1 to L3). Claw lesion scoring was performed in the farrowing stable: 1 week before weaning and 1 week after farrowing (C1 and C2). Reproduction data of one period were considered (breeding performance, farrowing performance and crushed piglets). C1, C2 = claw lesion score; L1, L2, L3 = lameness assessment 1, 2 and 3.

Figure 2

Table 2 Overview of the farrowing and breeding performance of the sows in the study

Figure 3

Table 3 Final multivariable logistic regression models related to the risk factors for farrowing performance and crushed piglets with farm, parity, claw score and lameness as independent variables and presence of stillborn piglets, mummified foetuses and crushed piglets as dependent variables

Figure 4

Figure 2 Percentage of sows (total of 381) with and without lesions for each of the seven claw parameters that were scored at the first (1) and second (2) time claw lesion scoring was carried out. 1, performed at the end of the first lactation period, at the beginning of the study; 2, performed 5 days after parturition in the second lactation period, at the end of the study.

Figure 5

Figure 3 Percentage of sows that were lame at the three visual lameness assessments (L1 to L3) for each farm (F1 to F5).