Effect of administration of a controlled-release monensin capsule on incidence of calving-related disorders, fertility, and milk yield in dairy cows

Pedro Melendez Department of Large Animal Clinical Sciences, College of Veterinary Medicine, University of Florida, Gainesville, FL 32610-0136.

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Jesse P. Goff National Animal Disease Center, USDA, Ames, IA 50010.

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Carlos A. Risco Department of Large Animal Clinical Sciences, College of Veterinary Medicine, University of Florida, Gainesville, FL 32610-0136.

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Louis F. Archbald Department of Large Animal Clinical Sciences, College of Veterinary Medicine, University of Florida, Gainesville, FL 32610-0136.

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Ramon C. Littell Institute of Food and Agriculture Sciences, University of Florida, Gainesville, FL 32610-0136.

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G. Arthur Donovan Department of Large Animal Clinical Sciences, College of Veterinary Medicine, University of Florida, Gainesville, FL 32610-0136.

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Abstract

Objective—To determine the effect of a controlled-release monensin capsule administered at cessation of lactation on incidence of calving-related disorders, fertility, and milk yield in dairy cows.

Animals—290 dairy cows treated with monensin and 290 untreated control cows.

Procedure—Treated cows received a capsule that released monensin at 335 mg/d for 95 days. Incidence of calving-related disorders; daily milk yield up to 20 days postpartum; test-day milk yield, fat, protein, and mature-equivalent 305-day milk production; and body condition score at calving were determined. Reproductive variables were conception rate at first service, pregnancy rate, and calving-to-conception interval.

Results—Cows treated with monensin were 2.1 times as likely to develop dystocia and 0.8 times as likely to develop metritis as control cows. For milk yield, there was an interaction of treatment ×time ×parity. In multiparous cows, monensin significantly improved milk yield at test days 4 and 7. In addition, monensin increased body condition score at calving.

Conclusions and Clinical Relevance—Despite increasing the likelihood of developing dystocia and metritis, administration of monensin improved the lactational performance of multiparous cows and may be a promising additive for use at the time of cessation of lactation.

Abstract

Objective—To determine the effect of a controlled-release monensin capsule administered at cessation of lactation on incidence of calving-related disorders, fertility, and milk yield in dairy cows.

Animals—290 dairy cows treated with monensin and 290 untreated control cows.

Procedure—Treated cows received a capsule that released monensin at 335 mg/d for 95 days. Incidence of calving-related disorders; daily milk yield up to 20 days postpartum; test-day milk yield, fat, protein, and mature-equivalent 305-day milk production; and body condition score at calving were determined. Reproductive variables were conception rate at first service, pregnancy rate, and calving-to-conception interval.

Results—Cows treated with monensin were 2.1 times as likely to develop dystocia and 0.8 times as likely to develop metritis as control cows. For milk yield, there was an interaction of treatment ×time ×parity. In multiparous cows, monensin significantly improved milk yield at test days 4 and 7. In addition, monensin increased body condition score at calving.

Conclusions and Clinical Relevance—Despite increasing the likelihood of developing dystocia and metritis, administration of monensin improved the lactational performance of multiparous cows and may be a promising additive for use at the time of cessation of lactation.

The transition period in dairy cows is defined as 3 weeks before and 3 weeks after parturition and is characterized by tremendous physiologic and metabolic demands. Calving is a major component of this stage1; consequently, calving-related disorders, such as hypocalcemia, retained fetal membranes, metritis, fatty liver, ketosis, left and right displacement of the abomasum, mastitis, and lameness, are common conditions that have a negative economic impact on dairy herds.2 The negative impact of calving-related disorders on reproductive performance and milk production has been well documented.3 Therefore, any successful attempt to decrease the incidence of calving-related disorders will positively affect milk yield and fertility in dairy cows.

Monensin is an ionophore that affects rumen fermentation dynamics.4 The most consistent and well-documented fermentation alteration is increased proportion of propionic acid with a concurrent decrease in the proportion of acetate and butyrate.5 As a result, a lower incidence of ketosis and lipid mobilization–related disorders has been achieved.6,7

Monensin has been available for use in food animals for more than 20 years. However, limited information is available about its effect in lactating dairy cows. During the past 7 years, several research studies8–12 have been conducted in Canada and Australia on the use of monensin in the form of a controlled-release capsule. Monensin has recently been approved for use in lactating dairy cattle in the United States. We hypothesized that treatment with monensin in Holstein cows during use of typical Florida diets would be associated with a decrease in the incidence of calving-related disorders and an increase in milk production.

The purpose of the study reported here was to determine the effect of a controlled-release monensin capsule administered at cessation of lactation on the incidence of calving-related disorders, fertility, and milk yield during the transition period in dairy cows.

Materials and Methods

Cows and herd management

This study was approved by the Institutional Animal Care and Use Committee of the University of Florida, and use of the monensin controlled-release capsule was approved by the US FDA (INAD No. 10749). The study was conducted on a commercial dairy farm with 3,000 milking cows that were located in north-central Florida. Cows had a 305-day mean mature-equivalent milk production of 10,700 kg. Lactating cows were housed in a drylot system and were fed the same total mixed ration 3 times/d to meet or exceed the nutritional requirements of the National Research Council.13 Postpartum transition cows received a diet higher in neutral detergent fiber (Tables 1 and 2). Cows were managed to cease lactation from 50 to 70 days before expected parturition, housed in a drylot, and fed a diet typical for nonlactating Florida cows. At 21 days before expected parturition, dry cows were moved from the drylot to a different prepartum drylot and were considered to be prepartum transition cows. Twice per day, they were fed a diet with a dietary cation anion difference of −51.7 mEq/kg (dry matter basis) by use of the following equation:

article image

Table 1—

Composition of diets fed to prepartum and lactating dairy cows during 3 periods.

Feed componentPrepartum periodaPrepartum transition periodbLactating transition periodc
Alfalfa hay019.317.53
Coastal hay04.760
Cottonseed (whole)09.848.75
Corn silage44.9024.0628.50
Ryegrass silage15.2904.20
Corn hominy06.9813.54
Citrus pulp21.209.824.25
Soybean meal17.203.445.49
Wet brewer's grain010.744.07
Lactating concentrate007.03
Lactowhey*03.764.23
Energy supplement02.791.96
Springer minerals04.510
Nonlactating cow minerals1.4100
Lactating cow minerals000.45

Values are percentage of diet on a dry matter basis.

Ammoniated whey (61.5% crude protein).

Energy supplement based on sodium propionate, propylene glycol, dried whey, and calcium carbonate.

Springer minerals are minerals given for approximately 21 days before parturition.

70 to 21 days before expected parturition.

21 days before expected parturition to calving.

Calving to 21 days postpartum.

Table 2—

Nutrient content of diets fed to prepartum and lactating dairy cows during 3 periods.

NutrientPrepartum periodaPrepartum transition periodbLactating transition periodc
CP (DM)*15.5217.9118.60
Undegradable protein (% CP)26.3835.3130.34
Degradable protein (% CP)73.6264.6969.66
Soluble protein (% CP)unknown36.7239.77
Net energy lactation (Mcal/kg)§0.841.691.69
Acid detergent fiber (% DM)*24.5425.1323.66
Neutral detergent fiber (% DM)*36.0436.2034.63
Nonfiber carbohydrates (% DM)32.9431.5534.13
Starch (% DM)11.0514.9614.90
Lipid (% DM)*2.856.202.36
Ca (% DM)*0.741.271.10
P (% DM)*0.300.350.46
Mg (% DM)*0.320.360.36
K (% DM)*1.281.101.46
Na (% DM)*0.090.090.58
Cl (% DM)*0.180.430.48
S (% DM)*0.240.40.22
Forage in diet (% DM)60.2148.1050.23
Dietary cation-anion difference (mEq/kg [DM])§165.9−51.7351.9

Laboratory nutritional analysis.

Values from feed composition tables.

From formulas after laboratory analysis.

From formula (Na+ + K+)- (Cl + S).

CP = crude protein. DM = Dry matter.

Cows calved in the drylot, and the calf was immediately separated from the dam at parturition. If the cow needed calving assistance, it was moved to a maternity barn. Cows were processed within 12 hours postpartum by use of a routine that included recording body condition score, udder score (for edema), reproductive tract status (trauma or lacerations), and whether the cow was suspected of having retained fetal membranes. If cows developed either retained fetal membranes or hypocalcemia, they were treated and remained in the hospital barn until recovery. After processing, cows were moved to a postpartum lot and fed a lactation diet high in forage neutral detergent fiber (Tables 1 and 2). Within 21 days postpartum (now considered postpartum transition cows), cows were monitored daily on the basis of their milk yield for the development of metritis, ketosis, and displacement of the abomasum. Any condition was recorded and treated accordingly.

Beginning 60 days postpartum, cows received bovine somatotropina SC every 14 days during the entire lactation. Reproductive management included a waiting period of 80 days until first insemination. First service was synchronized and used a timed artificial insemination protocol. Thereafter, cows were identified as being in estrus by use of visual observation or a computerized pedometer systemb and inseminated at estrus. Pregnancy diagnosis was performed by herd veterinarians via palpation per rectum of the uterus and its contents at approximately 42 to 49 days after insemination. Lactating cows were tested for milk yield, milk solids, and somatic cell count once per month by the DHIA.c

Experimental protocol

During July to August 2001, 580 cows at 50 to 70 days before expected parturition were randomly assigned to either a treatment or control group. The treated group (n = 290) received orally a capsule of monensind designed to remain in the rumen and release 335 mg of monesin daily for 95 days. Control cows (no capsule; n = 290) were randomly matched by parity (1, 2, and ≥ 3) and categorized as primiparous (parity 1) and multiparous (parity ≥ 2). The number of animals per treatment was calculated with the expectation of a reduction in the incidence of retained fetal membranes or metritis of 6% (95% confidence; 80% power).14

Outcome variables and case definitions

Outcome variables were the incidence of dystocia, clinical hypocalcemia, retained fetal membranes, metritis, clinical ketosis, displacement of the abomasum, and culling rate. Incidence was defined as the number of specified new cases during the lactation period of risk for that condition divided by the total number of cows in that group. Case definitions were mainly based on a previous report by Kelton et al.2 Dystocia was defined as human intervention (2 or more people) involving forced extraction of the calf.3 Hypocalcemia was diagnosed in any cow detected within 72 hours after parturition with anorexia, CNS signs, staggering, various degrees of unconsciousness, and good response to IV administration of calcium. Retained fetal membranes were defined as visible fetal membranes at the vulva, vagina, or uterus as detected via physical examination more than 24 hours after calving. Metritis was defined as any abnormal vaginal discharge or uterine content (foul smelling) obtained via rectal palpation.2,3 Ketosis was defined as a decrease in milk production and high concentration of urine ketones (> 40 mg/dL), as measured with a commercial test that has moderate sensitivity and high specificity.e Displacement of the abomasum was defined as decreased milk yield accompanied by an audible high-pitched tympanic resonance elicited by percussion of the left or right abdominal wall between the 9th and 12th rib spaces, with or without colic pain and confirmed via surgical intervention. Culling rate was defined as the number of cows that were removed from the herd for any reason before 410 days postpartum divided by the number of cows that were enrolled in the trial. Other outcome variables were daily milk yield up to 20 days postpartum and milk production, milk fat, and protein content at the first 10 DHIA test days during lactation. Mature-equivalent 305-day milk production was also recorded on the basis of DHIA information. Body condition score was determined at assignment, calving, and 60 days postpartum, according to a standard methodology15 and by the same person.

Reproductive variables used to evaluate fertility were conception rate at first service, pregnancy rate, and calvingto-conception interval. Conception rate at first service was defined as the number of cows pregnant at their first service divided by the number of cows inseminated for the first time after calving. Pregnancy rate was defined as the number of cows that became pregnant up to 410 days of lactation divided by the number of cows inseminated at least once during that period. Calving-to-conception interval was defined as the mean days between calving and the breeding date at which cows were confirmed pregnant.

Statistical analysis

The null hypothesis was that there was no difference in the incidence of calving-related disorders and other outcomes between groups. Incidences of calvingrelated disorders were analyzed by use of logistic regression, corrected for parity (primiparous or multiparous) and body condition score at calving (≥ 3.25 or < 3.25). Models for retained fetal membranes and metritis were additionally corrected for dystocia. A backward-elimination procedure was conducted for each model. Treatment was forced into the final models. To determine the degree of association between risk factors and outcome variables, odd ratios and 95% confidence intervals were calculated. Milk yield was analyzed by constructing a mixed model for repeated measures. Body condition score at assignment was included as a covariate in the model. A triple-interaction effect of treatment × test day × parity was conducted to test the parallelism of milk curves. Body condition score at calving was analyzed by use of the Wilcoxon rank test within parity (Shapiro-Wilk test; P < 0.01) and by use of ANOVA for testing the interaction of treatment × parity. Overall pregnancy rate was analyzed by use of survival analysis. Conception rate at first service was analyzed by use of logistic regression as described for calving-related disorders. Calving-to-conception interval was analyzed by use of an ANOVA linear model. Differences were considered significant at P ≤ 0.05. Statistical analyses were conducted by use of the corresponding procedure in a software program.16 Sample size was calculated by use of software.f

Results

The incidences of calving-related disorders and a summary of logistic regression modeling for significant variables were determined (Tables 3 and 4). Only dystocia and metritis were affected by treatment. Cows treated with monensin were 2.1 times as likely to develop dystocia as control cows. Correcting for parity and dystocia, treated cows were 0.8 times as likely to develop metritis as control cows. Cows with dystocia and cows in first lactation were, respectively, 19.2 and 5.7 times as likely to develop metritis as cows calving unassisted or older cows.

Table 3—

True incidence (% [nonadjusted]) of calving-related disorders in 290 control cows and 290 cows treated with monensin.

DisorderControlMonensin
Dystocia7.930.9*
Hypocalcemia0.00.0
RFM19.722.8
Metritis42.633.8*
Ketosis2.52.8
DA1.40.7
Culling rate28.628.6

Significant (P ≤ 0.05) difference from the control group.

RFM = Retained fetal membranes. DA = Displaced abomasum.

Table 4—

Summary of logistic regression modeling for calving-related disorders in cows treated with monensin.

ModelCoefficients
DependentExplanatoryOR95% CIP value
DystociaMonensin (yes)2.101.39–3.17< 0.01
Parity (primiparous)0.650.43–0.990.049
MetritisMonensin (yes)0.800.70–0.88<0.01
Parity (primiparous)5.653.25–9.82<0.01
Dystocia (yes)19.210.7–38.0<0.01

OR = Odds ratio. CI = Confidence interval.

For body condition score at calving, main effects of parity and treatment were significant. However, the interaction was not significant. Therefore, monensin increased body condition score at calving in both primiparous and multiparous cows (Figure 1; Table 5).

Table 5—

Descriptive statistics for body condition score (BCS) at calving by treatment and parity in control cows and cows treated with monensin.

VariablenMean BCSSEMMedianSkewnessKurtosis
Monensin-primiparous1073.43*0.013.50.051.19
Control-primiparous1093.350.013.250.21−0.16
Monensin-multiparous1643.26*0.013.250.14−0.22
Control-multiparous1583.170.013.250.330.32

Significantly (P = 0.01) different from matching control group.

Figure 1—
Figure 1—

Frequency distribution (No. of cows) for body condition score at calving by treatment and parity in control cows and cows that were treated with monensin. MonPri = Monensin, primiparous. ConPri = Control, primiparous. MonMul = Monensin, multiparous. ConMul = Control, multiparous.

Citation: American Journal of Veterinary Research 67, 3; 10.2460/ajvr.67.3.537

Daily milk yield up to 20 days postpartum by parity and treatment was not significantly different between treatment groups. Evaluation of the effect of treatment on test-day milk yields for the entire lactation revealed a triple interaction of treatment × parity × test day (Figure 2; P = 0.01). For primiparous cows, curves of milk production were not significantly different, and for multiparous cows, curves were not parallel; values of test days 4 and 7 were significantly different between treated and control cows. Accumulated milk yields of the entire lactation were not significantly different in cows treated with monensin, compared with controls (mean ± SEM, 13,910 ± 185 kg vs 13,627 ± 185 kg, respectively). Milk fat percentage and milk protein percentage for treated and control cows and within parity were not significantly different over time.

Figure 2—
Figure 2—

Least squares mean ± SEM test-day milk yield by treatment and parity in control cows and cows treated with monensin. *Significant (P ≤ 0.05) difference from matching (parity) control group. See Figure 1 for key.

Citation: American Journal of Veterinary Research 67, 3; 10.2460/ajvr.67.3.537

Conception rates at first service were 21.7% and 25.2% for control and treated cows, respectively. Overall pregnancy rates were 53.9% and 58.1% for control and treated cows, respectively. Calving-to-conception interval was 180.2 and 170.4 days (SEM, 12.2 days) for control and treated cows, respectively. For the conception rate at first service and calving-to-conception interval, there was an interaction between treatment and body condition score at 60 days postpartum. Cows treated with monensin were 1.33 times as likely to become pregnant at first service as cows not treated with monensin, although only in cows with a body condition score ≥ 2.75 at 60 days postpartum. Calving-to-conception interval and services per conception were also improved significantly by monensin only in cows with a body condition score ≥ 2.75 at 60 days postpartum. Overall pregnancy rate was not significantly different between treated and control cows.

Discussion

Results of this study partially substantiated our hypothesis because the incidence of some calving-related disorders (dystocia and metritis) was affected by treatment during the transition period. The incidence of clinical hypocalcemia (0%) was consistent with the use of anionic salts in the prepartum period.17–20 In addition, results regarding clinical hypocalcemia were expected because we assumed that monensin would have no effect on calcium metabolism.

The incidence of retained fetal membranes of approximately 20% was high but consistent with results of a previous study21 conducted on the same farm and within the range of 1.3% to 39.2% cited in the literature.2 Perhaps the definition of retained fetal membranes was not consistent and farm personnel misclassified the condition. This might be an overestimation of the true incidence of the disease. The lack of treatment effect was expected because retention of fetal membranes is a multifactorial condition and other variables are more important predisposing factors for retained fetal membranes.22–24

The higher incidence of dystocia in older cows treated with monensin, compared with control cows, was unexpected. Although dystocia is also a multifactorial condition, those persons providing calving assistance were unaware of group assignments. An explanation for this finding could be that cows exposed to monensin for a longer period (70 to 50 days) had a significantly higher body condition score at calving than did controls. Therefore, fat deposition may have also occurred inside the pelvis or birth canal, which could reduce intrapelvic space. Higher body condition score at calving has been associated with a higher incidence of dystocia.25,26 Another explanation might be that treated cows might have had heavier calves because improved glucose metabolism in the dam may provide more glucose for the developing fetus.27 Unlike Canadian studies6,9,11 in which boluses were administered during the last 3 weeks of gestation, boluses were administered 50 to 70 days before expected parturition in the present study, and this may have substantially increased glucose availability for the fetus. In beef cattle, calves from heifers fed monensin had higher birth weights than those from control heifers.28,29 However, another study30 found no effect of monensin on calf birth weight. Because this outcome was unexpected, collection of calf birth weight data was not planned or performed.

The incidence of metritis in this study was in the upper portion of the range of values reported in the literature (30% to 40%).2 This high incidence might be attributable to our less-stringent definition and might be an overestimation of the true incidence. In the present study, abnormal vaginal discharge was used as a criterion. Other studies have used other criteria including body temperature, milk yield, uterine status at palpation, and vaginal discharge.31 In the present study, monensin treatment was associated with a lower incidence of metritis when corrected for dystocia and parity. This represents a pure effect of treatment on the occurrence of the uterine condition because dystocia and parity were also positively associated with metritis. An explanation for the positive effect of monensin treatment on metritis is speculative. Perhaps treated cows had a better metabolic status postpartum with less fat mobilization and less ketone body production than control cows. This may have allowed for better immune function and prevention of infection, which could lead to metritis. Hyperketonemia impairs chemotaxis, cytokine production, and phagocitic capacity of leukocytes.32 Indeed, monensin reduces the rate of intramammary infections in lactating dairy cows, suggesting that monensin, through its antiketogenic effect, can decrease immunosuppression in early lactation.33

The incidence of clinical ketosis was in the lower portion of the range (2% to 22%) reported by other authors.2 However, the main criteria used to diagnose ketosis in our trial were a decrease in milk yield and detection of ketone bodies in urine by use of a colorimetric field test based on nitropruside.e This might be an underestimation of the real incidence of the disease because the urine teste has moderate sensitivity and high specificity.34 There was no effect of treatment on clinical ketosis, although monensin is antiketogenic in dairy cattle.6,7,9,35 Most of the Canadian studies have focused on the effects of the bolus on subclinical ketosis rather than clinical ketosis. One of those studies36 found no difference in the incidence of clinical ketosis between treated and control cows. However, when data from different study populations were pooled to increase sample size, monensin decreased the incidence of clinical ketosis.36 An explanation for the lack of treatment effect in the present study might be that the transition diet supplied 1.67 Mcal of net energy/kg for lactation and glucose precursors such as milk whey, sodium propionate, and propylene glycol. Perhaps this diet was sufficient to maintain better energy balance, normal glycemia, and a low incidence of clinical ketosis in transition cows, even without monensin treatment.

The incidence of abomasal displacement was in the lower portion of the range of 0.3% to 6.3% reported in the literature.2 There was no effect of treatment even though control cows had an incidence 2 times that in treated cows. The sample size, relative to the incidence of displacement of abomasum, reduced the power to detect differences attributable to treatment (power, 14%). Similar results were reported in 2 Canadian studies.7,36 A significant reduction of abomasal displacement associated with monensin as a bolus was found in both studies.

Culling rate was not significantly different between groups. Similar results were reported in a previous review.37 Overall, culling rate was within the expected range reported in the literature.38 Clinical hypocalcemia, retained fetal membranes, displacement of abomasum, ketosis, and ovarian cysts significantly affect culling at different stages of lactation. Metritis has no effect on culling.38 Because the incidences of clinical hypocalcemia, retained fetal membranes, displacement of the abomasum, and clinical ketosis in the present study were similar between treated and control cows, it seemed reasonable that culling rate was similar between groups.

Monensin given at cessation of lactation improved body condition score at calving. Within parity, control and treated cows had similar body condition score at cessation of lactation. However, body condition score was significantly higher in treated than control cows at calving. The effect of monensin as a growth promotant in beef and dairy cows has been described.30–39 However, in 1 study,30 dairy heifers treated with monensin did not have alterations in body composition, and in other studies,9,39,40 cows treated with monensin increased either body weight and body condition score or had reduced body condition score losses after calving. This is in agreement with the present study. Although monensin improved body condition score at calving, this improvement did not cause detrimental effects, other than dystocia, in cows. Another variable not evaluated in the present study that might increase body condition score at calving is the increment of energy density of the diet of nonlactating cows.13

In the present study, monensin treatment resulted in a slight nonsignificant increase in milk yield. This finding was consistent with previous studies10,12,41-44 in which monensin was used as a feed additive (premix) or a controlled-release bolus. Other studies11,45,46 did not find a positive effect of monensin on milk production. Monensin increased milk yield significantly on the basis of test-day milk yield in multiparous, but not first-lactation, cows. The positive effect of treatment might be explained by the fact that monensin improved body condition score at calving. Indeed, cows with a fair body condition score at calving are higher producers than thin and obese cows.10 In addition, phenotypic correlations between body condition score at calving and milk yield are slightly positive in Holstein cows.47 Monensin did not affect milk solids during the entire lactation. These results are in agreement with some studies44,46 but not all.41

The present study revealed differences in conception rate at first service and calving-to-conception interval between cows with and without monensin and with a body condition score ≥ 2.75 (an interaction effect) at 60 days postpartum. This finding is in agreement with other studies33,48 that revealed positive effects of monensin on reproductive responses. However, other studies7,44,49 found no effect of monensin on fertility variables. The fact that the effect of monensin was dependent on body condition score at 60 days postpartum emphasizes the important effects of energy balance and body condition score dynamics during the postpartum period on fertility in dairy cattle. In addition, because the bolus of monensin has a duration of 95 days, the positive effect of the ionophore on fertility could be attributable to improved body condition score at calving in cows treated with monensin during the entire nonlactating period (50 to 70 days prepartum).

DHIA

Dairy Herd Improvement Association

a

Posilac, 500-mg sometribove zinc, Monsanto, St Louis, Mo.

b

Afimilk, SAE Afikim, Kibbutz Afikim, Israel.

c

DHIA, Raleigh, NC.

d

CRC Rumensin, Elanco Animal Health, Guelph, ON, Canada.

e

Ketostix, Bayer Corp, Elkhart, Ind.

f

WinEpiscope, version 2.0, software for quantitative veterinary epidemiology. Delphi, version 1.0, Available at: www.clive.ed.ac.uk/winepiscope/. Accessed 2005.

References

  • 1

    Grummer RR. Impact of changes in organic nutrient metabolism on feeding the transition dairy cow. J Anim Sci 1995;73:28202833.

  • 2

    Kelton DF, Lissemore KD, Martin RE. Recommendations for recording and calculating the incidence of selected clinical diseases of dairy cattle. J Dairy Sci 1998;81:25022509.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 3

    Fourichon C, Seegers H, Bareille N, et al.Effects of disease on milk production in the dairy cow: a review. Prev Vet Med 1999;41:135.

  • 4

    Van Maanen RW, Herbein JH, McGilliard AD, et al.Effects of monensin on in vivo rumen propionate production and blood glucose kinetics in cattle. J Nutr 1978;108:10021007.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 5

    Richardson LF, Raun AP, Potter EL, et al.Effect of monensin on rumen fermentation in vitro and in vivo. J Anim Sci 1976;43:657664.

  • 6

    Duffield TF, Sandals D, Leslie KE, et al.Efficacy of monensin for the prevention of subclinical ketosis in lactating dairy cows. J Dairy Sci 1998;81:28662873.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 7

    Duffield TF, Leslie KE, Sandals D, et al.Effect of a monensin-controlled release capsule on cow health and reproductive performance. J Dairy Sci 1999;82:23772384.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 8

    Stephenson KA, Lean IJ, Hyde ML, et al.Effects of monensin on the metabolism of periparturient dairy cows. J Dairy Sci 1997;80:830837.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 9

    Duffield TF, Sandals D, Leslie KE, et al.Effect of prepartum administration of monensin in a controlled-release capsule on postpartum energy indicators in lactating dairy cows. J Dairy Sci 1998;81:23542361.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 10

    Duffield TF, Leslie KE, Sandals D, et al.Effect of prepartum administration of monensin in a controlled-release capsule on milk production and milk components in early lactation. J Dairy Sci 1999;82:272279.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 11

    Green BL, McBride BW, Sandals D, et al.The impact of a monensin controlled-released capsule on subclinical ketosis in the transition dairy cows. J Dairy Sci 1999;82:333342.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 12

    Mutsvangwa T, Walton JP, Plaizier JC, et al.Effects of a monensin controlled-release capsule or premix on attenuation of subacute ruminal acidosis in dairy cows. J Dairy Sci 2002;85:34543461.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 13

    National Research Council. Nutrient requirements of dairy cattle. 7th revised ed. Washington, DC: National Academy Press, 2001.

  • 14

    Dohoo IR, Martin W, Stryhn H. Sample size. In: Dohoo IR, Martin W, Stryhn H, eds. Veterinary epidemiologic research. Charlottetown, PE, Canada: AVC Inc, 2003;2753.

    • Search Google Scholar
    • Export Citation
  • 15

    Ferguson JM, Galligan DT, Thomsen N. Principal descriptors of body condition score in Holstein cows. J Dairy Sci 1994;77:26952703.

  • 16

    Littell R, Milliken G, Stroup W, et al.SAS system for mixed models. Cary, NC: SAS Institute Inc, BBU Press, 1996.

  • 17

    Block E. Manipulating dietary anions and cations for prepartum dairy cows to reduce incidence of milk fever. J Dairy Sci 1984;67:29392948.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 18

    Goff JP, Horst RL, Mueller FJ, et al.Addition of chloride to a prepartal diet high in cations increases 1,25-dihydroxyvitamin D response to hypocalcemia preventing milk fever. J Dairy Sci 1991;74:38633871.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 19

    Block E. Manipulation of dietary cation-anion difference on nutritionally related production diseases, productivity, and metabolic responses of dairy cows. J Dairy Sci 1994;77:14371450.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 20

    Vagnoni DB, Oetzel GR. Effects of dietary cation-anion difference on the acid-base status of dry cows. J Dairy Sci 1998;81:16431652.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 21

    Melendez P, Donovan A, Risco CA, et al.Effect of calcium-energy supplements on calving-related disorders, fertility and milk yield during the transition period in cows fed anionic diets. Theriogenology 2003;60:843854.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 22

    Paisley LG, Mickelson WD, Anderson PB. Mechanisms and therapy for retained fetal membranes and uterine infections of cows: a review. Theriogenology 1986;25:353381.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 23

    Correa MT, Erb H, Scarlett J. Path analysis for seven postpartum disorders of Holstein cows. J Dairy Sci 1993;76:13051312.

  • 24

    Kimura K, Goff JP, Kehrli ME, et al.Decreased neutrophil function as a cause of retained placenta in dairy cattle. J Dairy Sci 2002;85:544550.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 25

    Hoffman PC, Brehm NM, Price SG, et al.Effect of accelerated postpubertal growth and early calving on lactation performance of primiparous Holstein heifers. J Dairy Sci 1996;79:20242031.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 26

    Chassagne M, Barnouin J, Chacornac JP. Risk factors for stillbirth in Holstein heifers under field conditions in France: a prospective survey. Theriogenology 1999;51:14771488.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 27

    Drackley JK, Overton TR, Douglas GN. Adaptations of glucose and long-chain fatty acid metabolism in liver of dairy cows during the periparturient period. J Dairy Sci 2001;84(suppl E):E100E112.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 28

    Clanton DC, England ME, Parrott JC. Effect of monensin on efficiency on production in beef cows. J Anim Sci 1981;53:873880.

  • 29

    Hixon DL, Fahey GC Jr, Kesler DJ, et al.Effects of creep feeding and monensin on reproductive performance and lactation of beef heifers. J Anim Sci 1982;55:467474.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 30

    Baile CA, McLaughlin CL, Chalupa WV, et al.Effects of monensin fed to replacement dairy heifers during the growing and gestation period upon growth, reproduction, and subsequent lactation. J Dairy Sci 1982;65:19411944.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 31

    Smith BI, Donovan GA, Risco C, et al.Comparison of various antibiotic treatments for cows diagnosed with toxic puerperal metritis. J Dairy Sci 1998;81:15551562.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 32

    Suriyasathaporn W, Heuer C, Noordhuizen-Stassen EN, et al.Hyperketonemia and the impairment of udder defense: a review. Vet Res 2000;31:397412.

  • 33

    Heuer C, Schukken YH, Jonker LJ, et al.Effect of monensin on blood ketone bodies, incidence and recurrence of disease and fertility in dairy cows. J Dairy Sci 2001;84:10851097.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 34

    Carrier J, Stewart S, Godden S, et al.Evaluation and use of three cowside tests for detection of subclinical ketosis in early postpartum cows. J Dairy Sci 2004;87:37253735.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 35

    Duffield TF, LeBlanc S, Bagg R, et al.Effect of a monensin controlled release capsule on metabolic parameters in transition dairy cows. J Dairy Sci 2003;86:11711176.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 36

    Duffield T, Bagg R, DesCoteaux L, et al.Prepartum monensin for the reduction of energy associated disease in postpartum dairy cows. J Dairy Sci 2002;85:397405.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 37

    Duffield T. Subclinical ketosis in lactating dairy cattle. Vet Clin North Am Food Anim Pract 2000;16:231253.

  • 38

    Radostits OM, Leslie KE, Fetrow J. Culling and genetic improvement programs for dairy herds. In: Radostits OM, Leslie KE, Fetrow J, eds. Herd health: food animal production medicine. 2nd ed. Philadelphia: WB Saunders Co, 1994;159182.

    • Search Google Scholar
    • Export Citation
  • 39

    Simpson RB, Chase CC, Hammond AC, et al.Average daily gain, blood metabolites, and body composition at first conception in Hereford, Senepol, and reciprocal crossbred heifers on two levels of winter nutrition and two summer grazing treatments. J Anim Sci 1998;76:396403.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 40

    Meinert RA, Yang CMJ, Heinrichs AJ, et al.Effect of monensin on growth, reproductive performance, and estimated body composition in Holstein heifers. J Dairy Sci 1992;75:257261.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 41

    Van der Werf JHJ, Jonker LJ, Oldenbroek JK. Effect of monensin on milk production by Holstein and Jersey cows. J Dairy Sci 1998;81:427433.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 42

    Phipps RH, Wilkinson JID, Jonker LJ, et al.Effect of monensin on milk production of Holstein-Friesian dairy cows. J Dairy Sci 2000;83:27892794.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 43

    Lean IJ, Curtis M, Dyson R, et al.Effects of sodium monensin on reproductive performance of dairy cattle. I. Effects on conception rates, calving to conception intervals, calving to heat and milk production in dairy cows. Aust Vet J 1994;71:273277.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 44

    Hayes DP, Pfeiffer DU, Williamson NB. Effect of intraruminal monensin capsules on reproductive performance and milk production of dairy cows fed pasture. J Dairy Sci 1996;79:10001008.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 45

    Abe N, Lean IJ, Rabiee A, et al.Effects of sodium monensin on reproductive performance of dairy cattle. II. Effects on metabolites in plasma, resumption of ovarian cyclicity and oestrus in lactating cows. Aust Vet J 1994;71:277282.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 46

    Vallimont JE, Varga GA, Arieli A, et al.Effects of prepartum somatotropin and monensin on metabolism and production of periparturient Holstein dairy cows. J Dairy Sci 2001;84:26072621.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 47

    Dechow CD, Rogers GW, Clay JS. Heritabilities and correlations among body condition scores, production traits, and reproductive performance. J Dairy Sci 2001;84:266275.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 48

    Tallam SK, Duffield TF, Leslie KE, et al.Ovarian follicular activity in lactating Holstein cows supplemented with monensin. J Dairy Sci 2003;86:34983507.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 49

    Beckett S, Lean I, Dyson R, et al.Effects of monensin on the reproduction, health and milk production of dairy cows. J Dairy Sci 1998;81:15631573.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 50

    Domecq JJ, Skidmore AL, Lloyd JW, et al.Relationships between body condition scores and conception at first artificial insemination in a large dairy herd of high yielding Holstein cows. J Dairy Sci 1997;80:113120.

    • Crossref
    • Search Google Scholar
    • Export Citation

Contributor Notes

Supported by North Florida Holstein LLC.

Dr. Donovan.
  • Figure 1—

    Frequency distribution (No. of cows) for body condition score at calving by treatment and parity in control cows and cows that were treated with monensin. MonPri = Monensin, primiparous. ConPri = Control, primiparous. MonMul = Monensin, multiparous. ConMul = Control, multiparous.

  • Figure 2—

    Least squares mean ± SEM test-day milk yield by treatment and parity in control cows and cows treated with monensin. *Significant (P ≤ 0.05) difference from matching (parity) control group. See Figure 1 for key.

  • 1

    Grummer RR. Impact of changes in organic nutrient metabolism on feeding the transition dairy cow. J Anim Sci 1995;73:28202833.

  • 2

    Kelton DF, Lissemore KD, Martin RE. Recommendations for recording and calculating the incidence of selected clinical diseases of dairy cattle. J Dairy Sci 1998;81:25022509.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 3

    Fourichon C, Seegers H, Bareille N, et al.Effects of disease on milk production in the dairy cow: a review. Prev Vet Med 1999;41:135.

  • 4

    Van Maanen RW, Herbein JH, McGilliard AD, et al.Effects of monensin on in vivo rumen propionate production and blood glucose kinetics in cattle. J Nutr 1978;108:10021007.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 5

    Richardson LF, Raun AP, Potter EL, et al.Effect of monensin on rumen fermentation in vitro and in vivo. J Anim Sci 1976;43:657664.

  • 6

    Duffield TF, Sandals D, Leslie KE, et al.Efficacy of monensin for the prevention of subclinical ketosis in lactating dairy cows. J Dairy Sci 1998;81:28662873.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 7

    Duffield TF, Leslie KE, Sandals D, et al.Effect of a monensin-controlled release capsule on cow health and reproductive performance. J Dairy Sci 1999;82:23772384.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 8

    Stephenson KA, Lean IJ, Hyde ML, et al.Effects of monensin on the metabolism of periparturient dairy cows. J Dairy Sci 1997;80:830837.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 9

    Duffield TF, Sandals D, Leslie KE, et al.Effect of prepartum administration of monensin in a controlled-release capsule on postpartum energy indicators in lactating dairy cows. J Dairy Sci 1998;81:23542361.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 10

    Duffield TF, Leslie KE, Sandals D, et al.Effect of prepartum administration of monensin in a controlled-release capsule on milk production and milk components in early lactation. J Dairy Sci 1999;82:272279.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 11

    Green BL, McBride BW, Sandals D, et al.The impact of a monensin controlled-released capsule on subclinical ketosis in the transition dairy cows. J Dairy Sci 1999;82:333342.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 12

    Mutsvangwa T, Walton JP, Plaizier JC, et al.Effects of a monensin controlled-release capsule or premix on attenuation of subacute ruminal acidosis in dairy cows. J Dairy Sci 2002;85:34543461.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 13

    National Research Council. Nutrient requirements of dairy cattle. 7th revised ed. Washington, DC: National Academy Press, 2001.

  • 14

    Dohoo IR, Martin W, Stryhn H. Sample size. In: Dohoo IR, Martin W, Stryhn H, eds. Veterinary epidemiologic research. Charlottetown, PE, Canada: AVC Inc, 2003;2753.

    • Search Google Scholar
    • Export Citation
  • 15

    Ferguson JM, Galligan DT, Thomsen N. Principal descriptors of body condition score in Holstein cows. J Dairy Sci 1994;77:26952703.

  • 16

    Littell R, Milliken G, Stroup W, et al.SAS system for mixed models. Cary, NC: SAS Institute Inc, BBU Press, 1996.

  • 17

    Block E. Manipulating dietary anions and cations for prepartum dairy cows to reduce incidence of milk fever. J Dairy Sci 1984;67:29392948.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 18

    Goff JP, Horst RL, Mueller FJ, et al.Addition of chloride to a prepartal diet high in cations increases 1,25-dihydroxyvitamin D response to hypocalcemia preventing milk fever. J Dairy Sci 1991;74:38633871.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 19

    Block E. Manipulation of dietary cation-anion difference on nutritionally related production diseases, productivity, and metabolic responses of dairy cows. J Dairy Sci 1994;77:14371450.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 20

    Vagnoni DB, Oetzel GR. Effects of dietary cation-anion difference on the acid-base status of dry cows. J Dairy Sci 1998;81:16431652.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 21

    Melendez P, Donovan A, Risco CA, et al.Effect of calcium-energy supplements on calving-related disorders, fertility and milk yield during the transition period in cows fed anionic diets. Theriogenology 2003;60:843854.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 22

    Paisley LG, Mickelson WD, Anderson PB. Mechanisms and therapy for retained fetal membranes and uterine infections of cows: a review. Theriogenology 1986;25:353381.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 23

    Correa MT, Erb H, Scarlett J. Path analysis for seven postpartum disorders of Holstein cows. J Dairy Sci 1993;76:13051312.

  • 24

    Kimura K, Goff JP, Kehrli ME, et al.Decreased neutrophil function as a cause of retained placenta in dairy cattle. J Dairy Sci 2002;85:544550.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 25

    Hoffman PC, Brehm NM, Price SG, et al.Effect of accelerated postpubertal growth and early calving on lactation performance of primiparous Holstein heifers. J Dairy Sci 1996;79:20242031.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 26

    Chassagne M, Barnouin J, Chacornac JP. Risk factors for stillbirth in Holstein heifers under field conditions in France: a prospective survey. Theriogenology 1999;51:14771488.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 27

    Drackley JK, Overton TR, Douglas GN. Adaptations of glucose and long-chain fatty acid metabolism in liver of dairy cows during the periparturient period. J Dairy Sci 2001;84(suppl E):E100E112.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 28

    Clanton DC, England ME, Parrott JC. Effect of monensin on efficiency on production in beef cows. J Anim Sci 1981;53:873880.

  • 29

    Hixon DL, Fahey GC Jr, Kesler DJ, et al.Effects of creep feeding and monensin on reproductive performance and lactation of beef heifers. J Anim Sci 1982;55:467474.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 30

    Baile CA, McLaughlin CL, Chalupa WV, et al.Effects of monensin fed to replacement dairy heifers during the growing and gestation period upon growth, reproduction, and subsequent lactation. J Dairy Sci 1982;65:19411944.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 31

    Smith BI, Donovan GA, Risco C, et al.Comparison of various antibiotic treatments for cows diagnosed with toxic puerperal metritis. J Dairy Sci 1998;81:15551562.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 32

    Suriyasathaporn W, Heuer C, Noordhuizen-Stassen EN, et al.Hyperketonemia and the impairment of udder defense: a review. Vet Res 2000;31:397412.

  • 33

    Heuer C, Schukken YH, Jonker LJ, et al.Effect of monensin on blood ketone bodies, incidence and recurrence of disease and fertility in dairy cows. J Dairy Sci 2001;84:10851097.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 34

    Carrier J, Stewart S, Godden S, et al.Evaluation and use of three cowside tests for detection of subclinical ketosis in early postpartum cows. J Dairy Sci 2004;87:37253735.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 35

    Duffield TF, LeBlanc S, Bagg R, et al.Effect of a monensin controlled release capsule on metabolic parameters in transition dairy cows. J Dairy Sci 2003;86:11711176.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 36

    Duffield T, Bagg R, DesCoteaux L, et al.Prepartum monensin for the reduction of energy associated disease in postpartum dairy cows. J Dairy Sci 2002;85:397405.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 37

    Duffield T. Subclinical ketosis in lactating dairy cattle. Vet Clin North Am Food Anim Pract 2000;16:231253.

  • 38

    Radostits OM, Leslie KE, Fetrow J. Culling and genetic improvement programs for dairy herds. In: Radostits OM, Leslie KE, Fetrow J, eds. Herd health: food animal production medicine. 2nd ed. Philadelphia: WB Saunders Co, 1994;159182.

    • Search Google Scholar
    • Export Citation
  • 39

    Simpson RB, Chase CC, Hammond AC, et al.Average daily gain, blood metabolites, and body composition at first conception in Hereford, Senepol, and reciprocal crossbred heifers on two levels of winter nutrition and two summer grazing treatments. J Anim Sci 1998;76:396403.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 40

    Meinert RA, Yang CMJ, Heinrichs AJ, et al.Effect of monensin on growth, reproductive performance, and estimated body composition in Holstein heifers. J Dairy Sci 1992;75:257261.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 41

    Van der Werf JHJ, Jonker LJ, Oldenbroek JK. Effect of monensin on milk production by Holstein and Jersey cows. J Dairy Sci 1998;81:427433.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 42

    Phipps RH, Wilkinson JID, Jonker LJ, et al.Effect of monensin on milk production of Holstein-Friesian dairy cows. J Dairy Sci 2000;83:27892794.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 43

    Lean IJ, Curtis M, Dyson R, et al.Effects of sodium monensin on reproductive performance of dairy cattle. I. Effects on conception rates, calving to conception intervals, calving to heat and milk production in dairy cows. Aust Vet J 1994;71:273277.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 44

    Hayes DP, Pfeiffer DU, Williamson NB. Effect of intraruminal monensin capsules on reproductive performance and milk production of dairy cows fed pasture. J Dairy Sci 1996;79:10001008.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 45

    Abe N, Lean IJ, Rabiee A, et al.Effects of sodium monensin on reproductive performance of dairy cattle. II. Effects on metabolites in plasma, resumption of ovarian cyclicity and oestrus in lactating cows. Aust Vet J 1994;71:277282.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 46

    Vallimont JE, Varga GA, Arieli A, et al.Effects of prepartum somatotropin and monensin on metabolism and production of periparturient Holstein dairy cows. J Dairy Sci 2001;84:26072621.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 47

    Dechow CD, Rogers GW, Clay JS. Heritabilities and correlations among body condition scores, production traits, and reproductive performance. J Dairy Sci 2001;84:266275.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 48

    Tallam SK, Duffield TF, Leslie KE, et al.Ovarian follicular activity in lactating Holstein cows supplemented with monensin. J Dairy Sci 2003;86:34983507.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 49

    Beckett S, Lean I, Dyson R, et al.Effects of monensin on the reproduction, health and milk production of dairy cows. J Dairy Sci 1998;81:15631573.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 50

    Domecq JJ, Skidmore AL, Lloyd JW, et al.Relationships between body condition scores and conception at first artificial insemination in a large dairy herd of high yielding Holstein cows. J Dairy Sci 1997;80:113120.

    • Crossref
    • Search Google Scholar
    • Export Citation

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