Theriogenology Question of the Month

Tiago J. Fernandes Equine Veterinary Medical Center, Doha, Qatar.

Search for other papers by Tiago J. Fernandes in
Current site
Google Scholar
PubMed
Close
 DVM
,
Florent David College of Health and Life Sciences, Hamad Bin Khalifa University, Doha, Qatar.

Search for other papers by Florent David in
Current site
Google Scholar
PubMed
Close
 DVM, MSc
,
Juan C. Samper Equine Veterinary Medical Center, Doha, Qatar.

Search for other papers by Juan C. Samper in
Current site
Google Scholar
PubMed
Close
 DVM, PhD
, and
Tatiana Vinardell College of Health and Life Sciences, Hamad Bin Khalifa University, Doha, Qatar.

Search for other papers by Tatiana Vinardell in
Current site
Google Scholar
PubMed
Close
 DVM, PhD

History

A 7-year-old 570-kg (1,254-lb) multiparous warmblood mare that was an embryo transfer recipient of an embryo recovered from a donor mare 8 days after ovulation was referred for pregnancy assessment monitoring purposes. Pregnancy had been diagnosed with transrectal ultrasonography 14 days after embryo transfer, and no further assessments had been performed since then.

On physical examination, the mare had a body condition score of 6 (on a scale of 1 to 9) and was bright, alert, and responsive. The mare's vital signs were within reference limits, and the duration of gestation at that point was reported to have been 144 days. With the mare restrained in stocks but not sedated, ultrasonographica examination was performed transrectally with an endolinear, transrectal multifrequency transducer (5 to 9 MHz) and transabdominally with a convex multifrequency transducer (2 to 6 MHz; Figure 1; Supplementary Figure S1, available at: avmajournals.avma.org/doi/suppl/10.2460/javma.258.12.1345).

Figure 1
Figure 1

Transabdominal ultrasonographic images of a fetus in utero on approximately day 144 of gestation in a 7-year-old 570-kg (1,254-lb) multiparous warmblood mare. A—Cross-sectional view (probe, 3.5 MHz) of the fetal right orbit showing the locations (dotted lines) for the 2 measurements of the combined orbital diameter. Fetal rostral is toward the upper right of the image, fetal dorsal is toward the upper left, and the mare's head is toward the upper right; the scale along the side of the image is in centimeters. B—Dorsal plane view (probe, 5.0 MHz) of the fetal cranium at the level of the widest dimension of the skull just dorsal to the fetal temporomandibular joints bilaterally, representing the location (dotted line) for measuring the biparietal diameter. The mare's head and fetal rostral are toward the upper left of the image. C—Oblique plane view (probe, 5.0 MHz) of the fetal cranium with the cursors positioned at the widest dimension (dotted line) of the skull in this image. Fetal rostral is toward the lower left of the image, the mare's head is toward the left of the image, and the scale along the side of the image is in centimeters. In all images, the yellow arrowhead indicates the center point of contact by the ultrasound transducer.

Citation: Journal of the American Veterinary Medical Association 258, 12; 10.2460/javma.258.12.1345

Question

What key abnormality was detected with ultrasonography?

Answer

The fetus had a severely malformed skull, consistent with congenital hydrocephalus.

Results

The fetus could not be palpated during rectal examination of the mare, which was an unusual finding for the stage of gestation. Mild cervical relaxation was detected on transrectal palpation and ultrasonographic examination, with a mean cervical diameter of 27.76 mm (reference range, 21.91 to 19.69 mm at 4 months of gestation). Additionally, the uteroplacental unit appeared corrugated. The mean combined thickness of the uterus and placenta at the cervical pole was 0.82 cm (reference range, 0.2 to 0.4 cm), and this abnormal finding was likely caused by the fetus and cranial aspect of the mare's uterus having been positioned far forward in the mare's abdominal cavity. (Supplementary Figure S2, available at: avmajournals.avma.org/doi/suppl/10.2460/javma.258.12.1345). The mare also had a small left uterine artery diameter (3.3 mm; reference range,1 6 to 7 mm for mares at 120 to 180 days of gestation). However, overall results of color flow Doppler ultrasonography indices of the uterine arteries, umbilical cord, and fetal carotid arteries suggested adequate fetoplacental perfusion. Additionally, the fetal aortic diameter at the anterior portion of the aorta during systole was 8.2 mm (reference range, 6 to 8 mm in midgestation), which indicated an adequate size for a fetus at day 144 of gestation. The fetal heart rate during rest and activity ranged between 130 and 155 beats/min, respectively (reference range, 120 to 140 beats/min at rest and in midgestation).

The fetus had a slightly large combined (width plus length) fetal eye orbital diameter (approx 45.1 mm; reference range, 38 to 40 mm; Figure 2). The eye width was measured from the anterior margin lens capsule to the inner margin of the optic disc, and eye length was measured across the maximum distance between the inner margins of the vitreous body. The fetal biparietal diameter (BPD) was 97.6 mm (reference range, 40 to 50 mm in midgestation), which was a measurement obtained with the ultrasound beam perpendicular to the fetal central axis at the level of the widest span of the cranium and where the space for the cerebral hemispheres appeared symmetric. For this measurement, the ultrasound calipers were placed at the outer edge of the near calvarial wall and inner edge of the far calvarial wall. The fetal BPD was disproportionately large, compared with the combined fetal orbital diameter, and suggested an excessively large skull for the gestational age. Measurements at the longest and widest dimensions of the fetal stomach and gonads were within reference limits.

Figure 2
Figure 2

Same images as in Figure 1, with an orientation toward the direction of the mare's head indicated in each image (blue dot). A—The fetal right eye is centered in the image. The combined orbit diameter (the sum of the distance [dotted line] between the anterior margin of the lens capsule [yellow arrow] and area of the optic disc [green arrow; eye width {purple arrowheads} = 21.9 mm] and the longest distance between the inner margins of the vitreous body [eye length {dotted line connecting the orange arrowheads} = 23.2 mm]) for the right orbit is 45.1 mm (reference range, 38 to 40 mm). B—The dorsal plane fetal biparietal diameter is 97.6 cm (dotted lines connecting the red arrowheads). C—In this oblique view of the cranium, the widest dimension of the skull is 101 mm (dotted line connecting the pink arrowheads).

Citation: Journal of the American Veterinary Medical Association 258, 12; 10.2460/javma.258.12.1345

Discussion

Clinical assessment of fetoplacental well-being by use of transabdominal ultrasonography during the second half of gestation in mares is a valid diagnostic tool.2 However, this type of examination is not performed as routinely in horses as it is in people, in whom fetal growth during the last trimester is assessed more stringently and comprehensively, including measurements of the fetal femur length, BPD, head circumference, abdominal diameter, and abdominal circumference.

In the mare of the present report, ultrasonography revealed a fetus with a severely enlarged BPD (97.6 mm) that was incompatible with the gestational age of the fetus and consistent with congenital hydrocephalus. Few reports3,4 have described the diagnosis of congenital hydrocephalus in neonatal foals, and MRI is preferred for detecting structural abnormalities of the head in newborn foals.4 However, 2-D ultrasonography is an ideal tool to assess the fetus during gestation; the modality is cost-effective, provides real-time imaging with high resolution, and is safer for the mare and fetus.

Hydrocephalus occurs through disruption of the normal flow of CSF from its point of formation in the choroid plexus to its point of absorption at the arachnoid villi in the venous sinuses. Consequently, the intracranial pressure increases, causing distension of the ventricular system of the brain and enlargement of the skull.2 Hydrocephalus is an uncommon condition associated with dystocia in mares, with an estimated prevalence of hydrocephalus of 0.6 affected foals/1,000 births.5 Furthermore, congenital hydrocephalus is considered an autosomal recessive hereditary condition associated with a mutation in the B3GALNT2 gene, with higher prevalence in Friesian and Belgian horses (vs other breeds) owing to their limited genetic pools.6,7 The genetic profile of the fetus of the present report was not investigated.

Ultrasonographic examination of the mare of the present report also revealed a disparity in the diameters of the right and left uterine arteries (7.9 and 3.3 mm, respectively), whereas the diameters of both uterine arteries generally increase linearly throughout pregnancy and with the parity of the mare.1 The smaller diameter of the left uterine artery did not affect the overall size of the fetus, and whereas small fetal aortic and orbital diameters are often associated with high-risk pregnancies, those measurements for the fetus in the present report were within reference limits for its gestational age.8

The findings for the fetus highlighted the importance of transabdominal ultrasonographic examination to identify fetal abnormalities in horses. To our knowledge, this report was the first to describe ultrasonographic findings of fetal hydrocephalus in utero. We strongly suggest veterinarians perform transabdominal ultrasonography in addition to transrectal ultrasonography to monitor fetal development and growth throughout gestation in horses. This combination of ultrasonographic examination procedures is a valuable tool for evaluating high-risk pregnancies, identifying abnormalities during fetal development, and gathering clinically relevant information to help prepare for optimal outcomes of gestation.

Outcome

Because of a poor prognosis for fetal survival and a high risk of complications for the mare, the owners elected to hospitalize the mare and induce parturition. The mare was treated with cloprostenol (0.55 μg/kg [0.25 μg/lb], IM) and misoprostol (2 μg/kg [0.9 μg/lb]; mixed with 10 mL of sterile lubricating gel and applied topically to the cervix). Approximately 2 hours later, preterm parturition had advanced to the point that manual assistance could be provided for vaginal delivery of the fetus. A stillborn fetus was delivered. The fetus had thin and craniodorsally distended bones of the calvarium, consistent with hydrocephalus (Figure 3). The uterine fluid and placenta were grossly normal for the stage of gestation. Physical and ultrasonographic examination postpartum revealed anechoic uterine intraluminal fluid accumulation (diameter, approx 3.4 cm) in the uterine body and no trauma to the mare's reproductive tract.

Figure 3
Figure 3

Picture of the fetus described in Figure 1 showing its severely enlarged and thin-boned cranium (arrow).

Citation: Journal of the American Veterinary Medical Association 258, 12; 10.2460/javma.258.12.1345

The mare was treated with oxytocin (20 U total, IM, q 1 h for 6 hours, then q 3 h for 18 hours) and underwent uterine lavage with 5 L of lactated Ringer solution every 12 hours for 2 days. The mare progressed well and was discharged with a prescription for oxytocin (20 U total, IM, q 6 h for 3 days) 3 days after the initial examination. When the mare was returned for a recheck examination 3 months later, findings were unremarkable and the decision was made to enroll the mare as a recipient in another embryo transfer program.

Footnotes

a.

LOGIQ e R7, GE Healthcare, Chicago, Ill.

References

  • 1.

    Ousey JC, Kölling M, Newton R, et al. 2012. Uterine haemodynamics in young and aged pregnant mares measured using Doppler ultrasonography. Equine Vet J Suppl 2012;44:1521.

    • Search Google Scholar
    • Export Citation
  • 2.

    Bucca S, Fogarty U, Collins A, et al. Assessment of feto-placental well-being in the mare from mid gestation to term: transrectal and transabdominal ultrasonographic features. Theriogenology 2005;64:542557.

    • Search Google Scholar
    • Export Citation
  • 3.

    Ferris RA, Sonnis J, Webb B, et al. 2011. Hydrocephalus in an American Miniature Horse foal: a case report and review. J Equine Vet Sci 2001;31:611614.

    • Search Google Scholar
    • Export Citation
  • 4.

    Oey L, Müller JM, von Klopmann T, et al. Diagnosis of internal and external hydrocephalus in a warmblood foal using magnetic resonance imaging. Tierarztl Prax Ausg G Grosstiere Nutztiere 2011;39:4145.

    • Search Google Scholar
    • Export Citation
  • 5.

    Ricketts SW, Barrelet A, Whitwell KE. Equine abortion. Equine Vet Educ 2003;15:1821.

  • 6.

    Ducro BJ, Schurink A, Bastiaansen JWM, et al. A nonsense mutation in B3GALNT2 is concordant with hydrocephalus in Friesian horses. BMC Genomics 2015;16:761.

    • Search Google Scholar
    • Export Citation
  • 7.

    Kolb DS, Klein C. Congenital hydrocephalus in a Belgian draft horse associated with a nonsense mutation in B3GALNT2. Can Vet J 2019;60:197198.

    • Search Google Scholar
    • Export Citation
  • 8.

    Renaudin CD, Gillis CL, Tarantal AF, et al. Evaluation of equine fetal growth from day 100 of gestation to parturition by ultrasonography. J Reprod Fertil Suppl 2000;56:651660.

    • Search Google Scholar
    • Export Citation
All Time Past Year Past 30 Days
Abstract Views 0 0 0
Full Text Views 1492 982 30
PDF Downloads 490 135 7
Advertisement