This study aimed to identify risk factors affecting PBW, high CV_PBW and the occurrence of IUGR piglets in 12 commercial Danish herds with hyperprolific sows using free-access stalls, floor or electronic sow feeding systems in the gestation unit. The following factors were investigated: the duration of previous lactation, the length of the interval from weaning to insemination, the length of gestation, litter size, parity, sow backfat thickness in late gestation and the type of feeding system in the gestation unit. The study included newborn piglets from 452 litters with the following production indicator averages: 21.3 piglets/L, 1235 g PBW, 22.9% CV_PBW and 10.9% and 11.8% within-litter occurrence of severe and mild IUGR piglets, respectively. Increasing length of weaning-to-insemination interval decreased PBW by 25.8 g/day. For 2nd to 9th parity sows, each additional piglet in the litter increased CV_PBW by 0.38%, the occurrence of severe IUGR piglets by 0.68% and mild IUGR piglets by 0.50%. Sows of 5th parity and older had a 1.39% higher CV_PBW and 49.1 g lighter piglets compared with sows of 2nd to 4th parity. PBW was lower in one ESF herd, suggesting complex interactions that need to be further elucidated. The main critical risk factor observed was litter size.

The aim of this study was to investigate herd cortisol levels as an indicator of stress during gestation in three different feeding systems. Twelve commercial Danish herds with 800 to 3050 sows were included, with either free-access feeding stall (Stall), floor feeding (Floor), or electronic sow feeding (ESF; n = 4 herds per system). Saliva samples were collected from 30 sows/herd in the gestation unit for cortisol analysis with an average of 67.2 gestation days for ESF, 72.4 days for Floor, and 68.6 days for Stall. Data on piglet birth weight (PBW) and the percentage of intrauterine growth restricted (IUGR) piglets from 452 litters (9652 piglets, 8677 liveborn) from all 12 herds were obtained on the saliva collection days. The cortisol levels in saliva increased throughout gestation (p < 0.01), and lower concentrations were observed among sows belonging to Stall (4.80 nmol/L), compared to Floor (7.03 nmol/L) and ESF (7.87 nmol/L), and that difference was significant as an independent effect in the case of ESF (p < 0.01). There was no difference between Floor and ESF or Stall and Floor (p > 0.05). An interaction was observed between parity and feeding system, with parities 4–5 in ESF herds having lower levels than other parities within the ESF system (p = 0.02).

Replacing stock is costly in any pig production. In addition, it takes time for young animals to reach the same level of productivity as more mature animals. Therefore, the aim of this study was to investigate the effects of long- or short-term increased feed allowance (covering the luteal and follicular phases) prior to service in the second estrus on first parity performance. In order to achieve this, altrenogest was used to synchronize the gilts cycle to allow a precise feeding strategy, and only gilts inseminated 0–10 d after altrenogest withdrawal were included in the study. Altrenogest was given at days 0–18 to control the luteal phase and, therefore, treatments covered different feeding strategies in either or both the luteal phase (days 0–18) and follicular phase (days 18–25). High feed allowance (H) was induced using 0.97 kg more feed per day compared to the low feed allowance (L) given 2.33 kg/d. Four feeding strategies, low–low (LL), high–high (HH), high–low (HL), and low–high (LH), were included. Once gilts had been inseminated, feed allowance was reduced to 2.23 kg/d to prevent the loss of embryos in early gestation. A tendency was observed between feeding strategy and backfat thickness before altrenogest treatment, showing that total born piglets were positively correlated to backfat in the LL and LH (no increased feed allowance or short-term increased feed allowance), treatments (P = 0.076), compared to when gilts had longer periods with high feed allowance (HH and HL). High feed allowance in the follicular phase (LH) tended to increase the number of total born piglets compared to the other groups (P = 0.069) when applied in the follicular phase of the second standing estrus after the gilts were given altrenogest. This would be equivalent to the last 5–7 d of a 21-d cycle in gilts. The three other feeding strategies, comprising either the luteal and follicular phases (HH) or the luteal phase (HL) or none (LL), did not increase litter size. The weight of the gilt when entering the insemination section also had an effect on total born piglets (P < 0.001) with an increase in litter size with increased weight of the sow, but no differences between treatments. In conclusion, the weight of the gilt had an influence on the total litter size and gilts with low backfat tended to respond more positively to a longer period with high feed allowance than fatter gilts.

This study investigated the impact of calcium (Ca) and vitamin D supplements on bone metabolism, bone measurement, lameness, and selection rate in gilts fed five dietary treatments. Two Ca levels (6.85/6.42 [adequate; ACa] or 8.99/8.56 [high; HCa] g/kg) were combined with either 856 IU/kg vitamin D3 (Danish feeding standards; adequate; AD3) or 50 μg/kg 25-hydroxyvitamin D3 (high; HHyD) to create ACaAD3, HCaAD3, ACaHHyD, and HCaHHyD diets. The values 6.85/6.42 and 8.99/8.56 g/kg correspond to adequate and high Ca supply for gilts weighing 32 to 100 and 100 to 180 kg body weight (BW), respectively. The fifth diet was a combination of HCa and 2,000 IU/kg vitamin D3 (high; HD3) to create HCaHD3. Two hundred gilts were phase fed the dietary treatments from 32 to 100 and 100 to 180 kg BW until they were slaughtered, either at 100 or 180 kg BW. The gilts were weighed fortnightly, and plasma and urine samples were collected at 100 and 180 kg BW. At slaughter, the 2nd and 3rd metacarpal bones were collected for bone parameters measurements. Lameness and selection rate were assessed within the last 7 d at 100 and 180 kg BW. Dietary treatments did not affect gilts’ growth performance and plasma concentration of Ca, but urinary concentration of Ca was greater in HCa-supplemented gilts at both 100 (P = 0.003) and 180 (P = 0.05) kg BW. Plasma concentration of vitamin D3 (P < 0.001) and 25-hydroxyvitamin D3 (P < 0.001) showed dose-dependent responses at both 100 and 180 kg BW. Bone-specific alkaline phosphatase was greater (P = 0.02) in the plasma sample collected at 180 kg BW in gilts fed the HCaHD3 diet and tended to be greater in gilts fed the ACaAD3 diet (P = 0.06). The bone ash content (P = 0.02) was greater in gilts fed the HCaAD3 diet and slaughtered at 100 kg BW compared with gilts fed the ACaAD3 and ACaHHyD diets. However, bone weight, length, thickness, dry matter, and mineral content did not differ among the dietary treatments at both 100 and 180 kg BW (P > 0.05). Neither lameness nor selection rate was affected by the dietary treatments. The average daily gain of gilts weighing 32 to 100 and 100 to 180 kg BW showed a positive correlation with bone strength (r = 0.37; P < 0.001) and bone ash content (r = 0.24; P = 0.02), respectively. In conclusion, higher Ca and vitamin D3 supplementation slightly increased bone ash content but had no effect on lameness or selection rate of the gilts compared to those fed according to the Danish nutrient standards.