- Case report
- Open Access
Ethylene glycol toxicosis in milk-fed dairy calves
Acta Veterinaria Scandinavica volume 64, Article number: 7 (2022)
Ethylene glycol (EG) (antifreeze) toxicosis has mostly been reported in dogs and cats, while reports on EG toxicosis in cattle are sparse. We report EG toxicosis in 25 milk-fed calves associated with a leak in the cooling pipes in a milk taxi. The milk taxi was connected to a geothermal heating system in which EG was used as antifreeze.
Although the assistant responsible for feeding milk to the calves observed a few blue-colored droplets of liquid on the surface of the milk in the milk taxi and suspected EG contamination, the milk was fed to the calves. Within hours, the calves became depressed and some died within the next 2 days. Necropsy and histopathology revealed widespread severe acute renal tubular necrosis with numerous birefringent crystals in the tubular lumen. Biochemical analysis of serum showed severe damage to the kidneys (marked azotemia) and hypochloremia, hyponatremia and hyperkalemia; findings consisting with metabolic acidosis. After feeding the calves, the assistant inspected the milk taxi and found a leaking cooling pipe.
The suspected EG toxicosis was confirmed by the observation of renal tubular necrosis, numerous intratubular crystals, and metabolic acidosis. EG toxicosis due to leaking pipes connected to a geothermal heating system has not been reported previously. Alternative antifreeze products that are less toxic than EG are recommended for use if there is a risk of contamination of human and animal foodstuffs in case of a leak in the system.
Ethylene glycol (EG) is widely used in the plastic and synthetic textile industry, but is generally better known for its antifreeze properties, as utilized in e.g., automotive antifreeze. Commercial antifreeze products contain around 95% EG, as well as other compounds such as anticorrosive substances and tracer color. EG has no odor or color, is water-soluble and upon ingestion, humans have reported that the taste is bitter-sweet and it leaves a slightly warm sensation in the mouth. EG itself has a toxicity equivalent to ethanol, but EG is metabolized in the liver to glycolaldehyde, glycolic acid, glyoxylic acid and oxalic acid, which have cell toxic properties. Intoxication by these metabolites causes central nervous system (CNS) depression, as well as renal and cardio-pulmonary failure [1, 2].
In veterinary medicine, EG toxicosis is most commonly reported in dogs and cats , although rare episodes have been reported in other domestic animal species [4,5,6,7]. EG toxicosis in cattle is rarely reported. Barigye et al.  reported multiple deaths after feeding EG-contaminated plant by-products to group of adult beef cattle, while Crowell et al.  reported an isolated case in a 1-month-old Jersey calf that had access to antifreeze. In their report, Crowell et al. mention two additional incidents of EG toxicosis in cattle; both cases also related to the consumption of antifreeze from open containers. In this case study, we report an outbreak of EG toxicosis in dairy calves fed milk contaminated by EG via a leak in the milk cooling system, and we call for awareness whenever EG is used at cattle farms.
A Holstein dairy herd with 200 cattle experienced the sudden death of three out of a group of 25 milk-fed calves between May 22 and May 24, 2021. Milk used for feeding young calves in the herd was distributed by a milk taxi. The calves were fed around 3 L of whole milk twice a day. The calves had developed normally until the age of around 2 weeks, when they suddenly displayed reduced appetite and depression followed by apathy and death within one to two days. The owner regarded this as an isolated incident and did not consult the herd veterinarian or change procedures.
On June 10, the assistant responsible for feeding milk to the calves observed a small number of blue-colored droplets of liquid on the surface of the milk in the milk taxi. He suspected that the colored droplets were tracer color from the EG that was used in the herd’s bulk tank milk cooling (ice bank) system. When preparing milk for the calves, the ice bank system was temporarily connected to the milk taxi’s cooling system to ensure rapid cooling of the milk after pasteurization. The milk taxi was usually loaded with 70–80 L of milk. The assistant tasted the milk but did not detect any unexpected taste. He decided to feed the milk to the calves without knowing the toxicity of EG nor its concentration in the milk. After having fed the contents of the milk taxi to the calves, the assistant inspected the milk taxi’s cooling system and discovered a leak in a cooling pipe fitting (Fig. 1). Use of the milk taxi was immediately discontinued until the leak had been repaired. A fourth calf died on the same day with clinical signs similar to the previous three. Assistance from the herd veterinarian was requested the next day.
A fifth calf died during the night and the veterinarian found several diseased calves on June 11. The primary clinical signs were related to the CNS and consisted of stereotyped behavior, depression, paresis, seizure and salivation, with most calves only displaying stereotyped behavior and depression. The calves were not febrile. Blood samples for biochemical and hematological analyses were taken from two of the worst affected calves and submitted to LABOKLIN (Bad Kissingen, Germany). The serum biochemical analyses showed marked azotemia characterized by 4.3 and 3.7 times the upper reference limit (URL) of creatinine and 1.8 and 1.3 times the URL of urea in each calf, respectively. Electrolytes were also affected in both calves, characterized by hypochloremia (0.98; 0.97 times the lower reference limit (LRL)), hyponatremia (0.93; 0.95 times the LRL) and hyperkalemia (1.78; 1.42 times the URL). One calf also had hyperphosphatemia (1.17 times the URL). The liver-related membranous enzyme gamma glutamyltransferase (GGT) was increased in both calves (2.4 and 2.7 times the URL), while hypoproteinemia and hypoalbuminemia were also present. Hematological parameters were mildly affected and showed mild leukocytosis, neutrophilia and thrombocytosis. Complete biochemical and hematological data are shown in Tables 1 and 2.
Two of the recently dead calves were necropsied at the farm. The kidneys were enlarged and edematous with a soft cortex, while the liver was slightly enlarged. No other lesions were observed in the thoracic and abdominal organs. Specimens of the kidneys and liver were fixed in 10% neutral buffered formalin for histology and a sample of urine was taken for microscopy. Microscopy of urinary sediment after centrifugation revealed the presence of numerous calcium oxalate crystals. Histology of hematoxylin and eosin stained 4–5 µm paraffin embedded tissue sections of the kidneys showed severe widespread acute tubular necrosis, dilated tubuli and sloughing of necrotic tubular epithelial cells into the tubular lumen. Intratubular pale yellow crystals were widespread and associated with necrosis and loss of the tubular epithelium (Fig. 2). Viewing under polarized light revealed numerous birefringent crystals arranged in sheaves or rosettes. The crystals were more numerous in the renal cortex than in the medulla (Fig. 3). One of the calves also had renal interstitial fibrosis and lymphocytic infiltrations. The liver of one of the calves had scattered single-cell necrosis, while the other had mild steatosis.
Apart from avoiding any additional ingestion of EG, no specific treatment was initiated in the herd. Over the following days (until June 15), an additional 6 calves died, giving a total loss of 11 calves out of the 25 calves exposed to EG. The remaining calves recovered without displaying long-term clinical complications.
Discussion and conclusions
In the present case, a presumptive diagnosis of EG toxicosis was made based on the observation of blue-colored droplets in the milk fed to calves that subsequently became sick. A blue-colored EG-based antifreeze had been added to the milk cooling system. The diagnosis was confirmed by microscopic observation of renal tubular necrosis and the presence of numerous intratubular crystals; findings that are virtually pathognomonic for EG toxicosis . The presence of metabolic acidosis indicated by hyperkalemia, hyponatremia, and hypochloremia, and renal damage reflected by azotemia combined with hyperphosphatemia in one calf supported this diagnosis.
The observed kidney-related biochemical changes can be caused by a decreased glomerular filtration rate, tubular destruction and decreased resorption of analytes . In addition, increased GGT activity was identified, a finding that may be caused by toxic EG metabolites affecting the liver [12, 13]. However, GGT can also be released from proximal renal tubular epithelial cells but would then be expected to enter the urine rather than passing into the blood . The total protein and albumin concentrations were decreased, while the globulin concentration was within reference interval and similar to levels found in healthy Holstein calves evaluated for age-related changes in biochemistry values . The decreased protein and albumin concentrations may be explained by a combination of decreased production by the liver and increased loss of plasma albumin through the kidneys.
In contrast to the biochemical changes, the hematologic findings were mild with signs of stress-related changes, leukocytosis and neutrophilia, which have previously been identified in dogs and cats with EG intoxication [11, 16].
The susceptibility of cattle to EG intoxication is dependent on their age, as susceptibility decreases with increasing efficiency of ruminal fermentation. In an experimental study, a single oral dose of 2 mL to 5 mL of EG/kg body weight (BW) given to calves weighing 26–34 kg caused their deaths within three to six days. However, the toxicity of a single lower dose was not investigated, nor was the impact of repeated exposure to lower doses . It is therefore possible that much lower doses than 2 mL/kg BW or repeated exposure to lower doses would be toxic or even lethal to non-ruminating calves. The exposure dose in the present study could not be determined as the amount that leaked into the milk was unknown. However, it is likely that the calves were exposed repeatedly between May 22 and June 10, at least until a calf became clinically affected and stopped drinking milk. However, the exact exposure of each calf remains unknown.
EG is rapidly absorbed across the gastro-intestinal mucosa in mono-gastric species—and presumably also in non-fermentating ruminants—and plasma concentration peaks within a few hours. EG is not particularly toxic by itself and a significant amount is excreted unchanged in the urine within a few hours. However, EG is metabolized in the liver through a number of steps: it is first metabolized to glycoaldehyde, which is rapidly converted to glycolic acid. Glycolic acid is responsible for the severe metabolic acidosis that develops in cases of EG toxicosis , which was also observed in our case. Treatment of metabolic acidosis is essential for survival in the acute stage. Glycolic acid is metabolized to glyoxylic acid, which is toxic but has such a short half-life that toxic levels will not be reached. Glyoxylic acid can be metabolized through several pathways, with the formation of oxalic acid being of major significance. Oxalic acid is excreted through the urine, but precipitates with calcium in the glomerular ultrafiltrate to form calcium oxalate when pH decreases. Calcium oxalate crystals may damage the tubular epithelium and cause tubular obstruction, which is of particular importance for animals surviving acute toxicosis. However, precipitation may also lead to other pathological conditions such as low plasma calcium level . In dogs and cats, hypocalcemia can be seen in approximately half of the cases . The two calves investigated in our study had calcium concentrations within the reference intervals (Table 1).
Renal tubular damage in EG toxicosis is the result of two processes: toxic metabolites cause degeneration and necrosis of the tubular epithelium, while calcium oxalate crystals in the tubular lumen lead to the degeneration of epithelial cells and—depending on their numbers and size—may cause obstruction of the urinary flow. However, as the tubular basement membranes remain intact, regeneration can occur if the animal survives the acute toxicosis. If exposure to the nephrotoxin is discontinued, a normal-appearing tubular epithelium will return in seven to 14 days after last exposure, and the renal morphology will be completely normal 21 to 56 days after last exposure . In accordance with this, the calves that survived the acute toxicosis recovered.
The milk taxi’s cooling system was constructed in such a way that it could be connected to the ice-bank system of the farm’s bulk milk cooling tank to reduce water consumption and ensure rapid cooling of the milk after pasteurization. The cooling system of the ice-bank was connected to a geothermal heating system on the property, which contained several hundred liters of water with an EG concentration of around 30%. Adding antifreeze to the geothermal heating system is a requirement from the manufacturer. Due to financial reasons, EG was used as antifreeze at this property, instead of the more expensive propylene glycol or other less toxic compounds. This case illustrates the hazard associated with using EG in systems where the substance can come into direct contact with animal or human foodstuffs in case of leaking pipes, etc., and calls for awareness among veterinarians, agricultural advisors, technicians and farmers.
Availability of data and materials
The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.
Leth PM, Gregersen M. Ethylene glycol poisoning. Forensic Sci Int. 2005;155:179–84. https://doi.org/10.1016/j.forsciint.2004.11.012.
Kruse JA. Methanol and ethylene glycol intoxication. Crit Care Clin. 2012;28:661–711. https://doi.org/10.1016/j.ccc.2012.07.002.
Rowland J. Incidence of ethylene glycol intoxication in dogs and cats seen at Colorado State University Veterinary Teaching Hospital. Vet Hum Toxicol. 1987;29:41–4.
Osweiler GD, Eness PG. Ethylene glycol poisoning in swine. J Am Vet Med Assoc. 1972;160:746–9.
Boermans HJ, Ruegg PL, Leach M. Ethylene glycol toxicosis in a pygmy goat. J Am Vet Med Assoc. 1988;193:694–6.
Radi ZA, Miller DL, Thompson LJ. Ethylene glycol toxicosis in chickens. Vet Hum Toxicol. 2003;45:36–7.
APHA Disease Surveillance Report. Ethylene glycol poisoning in sheep. Vet Rec. 2015;176:515–8. https://doi.org/10.1136/vr.h2310.
Barigye R, Mostrom M, Dyer NW, Newell TK, Lardy GP. Ethylene glycol toxicosis in adult beef cattle fed contaminated feeds. Can Vet J. 2008;49:1018–20.
Crowell WA, Whitlock RH, Stout RC, Tyler DE. Ethylene glycol toxicosis in cattle. Cornell Vet. 1979;69:272–9.
Maxie MG, Newman SJ. Ethylene glycol. In: Maxie MG, editor. Jubb, Kennedy and Palmer’s Pathology of Domestic Animals, vol. 2. 5th ed. Edinburgh: Elsevier Saunders; 2007. p. 470–471.
Thrall MA, Grauer GF, Mero KN. Clinicopathologic findings in dogs and cats with ethylene glycol intoxication. J Am Vet Med Assoc. 1984;184:37–41.
Cable CS, Rebhun WC, Fortier LA. Cholelithiasis and cholecystitis in a dairy cow. J Am Vet Med Assoc. 1997;211:899–900.
Cebra CK, Garry FB, Getzy DM, Fettman MJ. Hepatic lipidosis in anorectic, lactating Holstein cattle: a retrospective study of serum biochemical abnormalities. J Vet Intern Med. 1997;11:231–7. https://doi.org/10.1111/j.1939-1676.1997.tb00096.x.
Garry F, Chew DJ, Hoffsis GF. Enzymuria as an index of renal damage in sheep with induced aminoglycoside nephrotoxicosis. Am J Vet Res. 1990;51:428–32.
Mohri M, Sharifi K, Eidi S. Hematology and serum biochemistry of Holstein dairy calves: age related changes and comparison with blood composition in adults. Res Vet Sci. 2007;83:30–9. https://doi.org/10.1016/j.rvsc.2006.10.017.
Connally HE, Thrall MA, Forney SD, Grauer GF, Hamar DW. Safety and efficacy of 4-methylpyrazole for treatment of suspected or confirmed ethylene glycol intoxication in dogs: 107 cases (1983–1995). J Am Vet Med Assoc. 1996;209:1880–3.
Beasley VR, Buck WB. Acute ethylene glycol toxicosis: a review. Vet Hum Toxicol. 1980;22:255–63.
Newman SJ, Confer AW, Panciera RJ. Acute tubular necrosis. In: McGavin MD, Zachary JF, editors. Pathologic Basis of Veterinary Disease. 4th ed. Maryland Heights: Elsevier; 2007. p. 645–657.
The authors thank the owner of the property for permission to conduct the study. Sarah Layhe is acknowledged for English language editing.
The study was funded entirely by internal institutional funds (e.g., covering the authors’ salaries).
Ethics approval and consent to participate
This case study did not require official or institutional ethical approval.
Consent for publication
The owner of property gave consent for the publication of data.
JSA is editor-in-chief of Acta Veterinaria Scandinavia, but has not in any way been involved in or interacted with the journal’s review process or editorial decision making. The editor was blinded to the review process. The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Agerholm, J.S., Hansen, K.S., Voogd, H.L. et al. Ethylene glycol toxicosis in milk-fed dairy calves. Acta Vet Scand 64, 7 (2022). https://doi.org/10.1186/s13028-022-00626-1
- Geothermal heating
- Milk taxi
- Tubular necrosis