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E v aluatio n
In the Field, at the Hospital, and After Surgery
a, b
Cristobal Navas de Solis, LV, PhD *, Michelle Coleman, DVM, PhD
KEYWORDS
Ultrasound Sonography Colic Gastrointestinal Abdominal
KEY POINTS
The use of abdominal sonography provides useful diagnostic and monitoring information
in the evaluation of horses with colic in the field, hospital, and postoperative setting.
During the last 4 decades, veterinarians have created a large body of literature informative
to clinicians using sonography to diagnose horses with colic.
It is likely that this technique will continue to advance in the near future as sonography be-
comes more available and affordable and newer generations of veterinarians receive more
and earlier training.
INTRODUCTION
a
Clinical Studies New Bolton Center, University of Pennsylvania; b Department of Large Animal
Medicine, University of Georgia
* Corresponding author.
E-mail address: navasdes@vet.upenn.edu
The current limitation of using this approach for decision-making is that pretest prob-
abilities are described in some situations yet hard to define in every setting, region, or
practice. Therefore, the clinical acumen of the veterinarian is key in the diagnostic pro-
cess. Furthermore, sonography is an operator-dependent technique and the diag-
nostic accuracy described in the literature may not apply to all operators. Finally, a
posttest probability is used differently for decision-making depending on the clinical
situation and therapies available.
Fig. 1. Small intestinal strangulation. Histologic (A), surgical (B), ex-vivo sonogram and
sonogram of the small intestine of a horse with a strangulated small intestinal lesion.
Note the distended nonmotile thickened intestine (D) and diffusely echoic wall correspond-
ing histopathologically to transmural hemorrhage (C). The yellow double headed arrow (C
and D) mark the small intestinal wall.
200 de Solis & Coleman
intestinal strangulation.1 The ability of a FLASH seems similar to a more detailed sono-
gram to detect small intestinal strangulation13 (Fig. 1).
The presence of increased peritoneal fluid, sedimented digesta within small intes-
tine or “two populations of intestine” with different appearance are often used as sup-
portive findings of strangulated lesions but the diagnostic accuracy of these findings
and overlap with other diseases such as nonstrangulated obstructions, functional ob-
structions, or an inflammatory processes is problematic. Overlap exists between the
sonographic findings in horses with strangulating lesions, nonstrangulating lesions,
and proximal enteritis. For example, early strangulated lesions may have intestine
with normal wall thickness.7 An elegant study investigated the association between
oxygen saturation in intestinal capillaries of horses with strangulated lesions and the
thickness of the wall measured sonographically.14 There was no association between
oxygen saturation and small intestinal wall thickness at the ischemic site. There was,
however, a negative correlation (thicker wall with decreasing oxygen saturation) in the
adjacent aboral segment. The authors suggested that venous occlusion leads to
decreasing oxygen saturation being associated with increasing wall thickness
(perhaps enhanced by surgical manipulation), and with arteriovenous occlusion, the
association is lost. Consequently, making conclusions about oxygen saturation based
on intestinal wall thickness is not possible. Intestinal wall thinning may be a late stage
of ischemia preceding rupture; however, it is rarely identified in the horse. Other recent
studies15,16 have investigated the association between sonographic and pathologic
findings in normal intestine and pathologic conditions (Fig. 2). Bevevino and collabo-
rators showed that intestinal wall layering and thickness of the different layers were
associated with the histologic appearance of the intestine and speculated that beyond
the intestinal wall thickness other sonographic characteristics may be useful to diag-
nose equine intestinal disease (Fig. 3). Characterization of the intestinal wall layering,
echogenicity, and blood flow may help, in the future, define further the presence and
stage of progression of strangulated or nonstrangulated lesions similar to the
described conditions such as necrotizing enterocolitis in humans.17,18 Pneumatosis
intestinalis (gas within the intestinal wall) is more commonly described in neonates
with necrotizing gastrointestinal disease19 and rarely in horses with strangulating le-
sions. Pneumatosis intestinalis is seen with other conditions causing necrosis such
as clostridial diseases, Lawsonia intracellularis infection (proliferative enteropathy),20
vascular compromise, or infarcts.
The sonographic appearance of the intestinal wall blood flow21 has not been thor-
oughly studied in the horse. In a preliminary study,21 the intestine blood flow could
not be detected in neonates using Doppler interrogation raising concerns about the
feasibility of this procedure. Since this study was performed, technology has improved
and equipment with more sensitive color-flow Doppler and motion correction algo-
rithms are currently available. Color-flow Doppler could be a useful technique in the
adult horse with colic similarly to its use in humans where Doppler signal with different
types of intestinal lesions is associated with histopathological findings and can be
used to guide therapeutic interventions.22–24 This concept would need to be tested
prospectively.
A high-yield finding in the evaluation of a horse with acute colic is the identification of
malpositioned mesenteric vessels. This finding has been reported in several
studies.25–27 Colonic blood vessels are normally located in the mesentery along the
medial aspect of the large colon and, therefore, obscured by digesta or gas. Colonic
Abdominal Sonographic Evaluation 201
Fig. 2. Composite depicts the histology of segments of the equine intestine with the basic
layers (mucosa, submucosa, muscularis, serosa) and corresponding in vitro sonographic
appearance of the basic sonographic layers. Inner hyperechoic layer 5 interface of contents
and mucosa, inner hypoechoic layer 5 mucosa, intermediate echoic layer 5 submucosa, in-
ner hypoechoic layer 5 muscularis, outer echoic layer 5 serosa. In the ileum, the muscularis
propria is thicker and the inner and outer muscularis layers separated by an echoic band are
more obvious than in the jejunum and duodenum. (A) Dudenum, (B) Jejunum, (C) Ileum, (D)
Cecum, (E) Right dorsal colon, (F) Small colon.
displacement or 180 volvulus leads to the medially located vessels becoming sono-
graphically visible laterally adjacent to the body wall. Medial colonic vessels occasion-
ally are visible in their normal location if the large intestine is fluid-filled. It is important
to recognize that 2 lateral cecal vessels (lateral cecal vessels and vessels of the cecal
arch) can be visible in the normal horse adjacent to the body wall from the middle
portion of the right flank caudal to costal arch and coursing cranioventrally. Therefore,
2 or more hypoechoic circular structures situated directly adjacent to the colon wall is
the sonographic criteria used to define this abnormality. These vessels are more
frequently identified in the middle aspect of the flank but the cranial to caudal, dorsal
to ventral location, and the number of intercostal spaces varies considerably27 (Fig. 4).
The changes in the diameter of the normal mesenteric vasculature or flow patterns
with different diagnoses have not been described.
Manso-Diaz and colleagues27 reported 34 horses presenting with acute colic asso-
ciated with large intestinal disease and sonographically visible dilated large colon
mesenteric vasculature. The visible vasculature on the right side of the abdomen
was associated with a diagnosis of right dorsal displacement of the large colon,
202 de Solis & Coleman
Fig. 3. Small intestinal thickening. Sonogram of a thickened loop of small intestine with a
prominent hypoechoic mucosa in a horse with anterior enteritis (A). Thickened (B1) and hy-
pervascular (B2) small intestinal wall with echoic loss of layering of the mucosa and submu-
cosa in a weanling with Lawsonia intracellularis infection (C). Thickened small intestine with
the loss of layering and echoic wall in a horse with a strangulating small intestinal lesion (D).
Thickened wall with prominent mucosa and muscularis in a horse with lymphoplasmacytic
inflammatory bowel disease. Double headed arrows mark small intestinal walls (A-D).
180 LCV, 540 LCV, or large colon impaction. A 540 LCV is uncommon, and clinical
findings of severe pain and shock often preclude transabdominal sonographic evalu-
ation and emergency surgery or euthanasia is indicated. When the vessels were
imaged on the left side of the abdomen, left dorsal displacement of the left colon,
180 LCV, or right dorsal displacement of the left colon were the described diagnoses.
If the malpositioned vessel was at the dorsal aspect of the left abdomen, left colon
displacement was the only diagnosis in this case series. Colonic vessels were imaged
bilaterally in one horse with a 180 LCV. Earlier studies had reported that sonographic
visualization of colonic mesenteric vessels provided a sensitivity of 67.7%, specificity
of 97.9%, positive predictive value of 95.8%, and negative predictive value of 81% for
right dorsal displacement or 180 LCV, or both.26 It is important to recognize that the
sonographic identification of colonic vessels adjacent to the body wall does not al-
ways necessitate exploratory laparotomy. This sonographic finding may, however,
be clinically useful to narrow the differential diagnosis list and to guide therapy in
conjunction with other clinical information.
The sonographic finding of severely thickened large intestine during the evaluation of a
horse with acute colic is interesting. The sonographic thickness of the intestine in clin-
ically normal horses and ponies is mean SD 1.8 0.03 mm to 4.2 0.3 mm.28,29
Severe large intestinal thickening (defined as wall thickness 9 mm) in the ventral
Abdominal Sonographic Evaluation 203
Fig. 4. Mesenteric vasculature and lymph nodes. Normal sonographic appearance of the
lateral cecal band (yellow arrow, A). Displaced and distended mesenteric vasculature in a
horse with colon volvulus (yellow arrow, B). Sonographically mild mesenteric lymphadenop-
athy in a horse with colitis (white arrow, C). Sonographically severe mesenteric lymphade-
nopathy in a horse with peritonitis (white arrow, D).
abdomen has been reported as a specific finding for the diagnosis of horses with
LCV30 in a population of horse with acute colic. It is important to recognize that other
causes of severe large intestinal thickening have been described including infectious
colitis, nonsteroidal anti-inflammatory drugs (NSAID) enteropathy/right dorsal colitis,
inflammatory bowel disease, colonic displacement, intestinal neoplasia, or intestinal
histoplasmosis. Although these diseases should be distinguishable from an LCV
based on clinical presentation, occasionally horses with these diseases can present
with acute and moderate-to-severe colic.31 For this reason, the 100% specificity
described by Pease and colleagues30 for their population, although informative,
may not be applicable to all clinical scenarios and the finding of a severely thickened
colon cannot always be attributed to LCV (Fig. 5).
A controversial finding is the presence of nonsacculated large colon in the left
ventral portion of the abdomen as an indication of LCV (180 or 540 ). This finding is
anatomically logical because these degrees of rotation position the nonsacculated
dorsal colon ventrally and the sacculated ventral colon dorsally away from the ventral
abdomen.32 However, the diagnostic accuracy of this finding is uncertain,33 and it is
likely that other clinical scenarios that cause slight rotations, colonic distension, or
heavy contents can cause the loss of ventral sacculations (eg, impactions or sand en-
teropathy among others).
Sand impactions are often seen sonographically as a flattened colon in the ventral
abdomen with hyperechoic contents that cast an acoustic shadow and reduced or
204 de Solis & Coleman
Fig. 5. Severe thickening of the colon. Sonogram of the colon of a horse with colitis caused
by salmonellosis (A). Sonogram of the colon of a horse with left dorsal displacement that
resolved without surgery (B). Sonogram of the colon in the cranial abdomen of a horse
with a LCV (C). Sonogram of the colon present in the caudal abdomen of horse (same horse
as in C) with a colon volvulus (D). Note the severely thickened colon in all images (yellow
arrows) that is echoic in (A) and (C), hypoechoic and striated in (B), and hypoechoic with
echoic submucosal patches in (D).
The inability to see the left kidney sonographically from the left flank has been classi-
cally used to diagnose nephrosplenic ligament entrapment of the large colon.35 Neph-
rosplenic entrapment and displacement of the large colon lateral to the spleen are
Abdominal Sonographic Evaluation 205
Fig. 6. Sonogram of a horse with sand impaction and enteropathy showing hyperechoic
contents (sand) in the colon (A), white single-headed arrow and echoic (normal digesta)
in another area of the colon (B), yellow single-headed arrow. The sonographic appearance
of the contents suggests sand and the radiograph confirms and quantifies the area of sand
(C). The high-frequency sonogram (D) shows the layered wall with mildly prominent submu-
cosa and subjectively mildly increased color flow signal suggesting enteropathy associated
with the presence of sand. The white double headed arrow (C) marks the sand dorsoventral
height.
collectively referred to as left dorsal displacement of the large colon. Lateral displace-
ments can resolve spontaneously whereas nephrosplenic ligament entrapments more
commonly require specific interventions.36 It has been suggested that if the sono-
graphic appearance of the dorsal aspect of the spleen is obliterated by a gas echo,
a diagnosis of nephrosplenic ligament entrapment can be made, whereas if the entire
image of the spleen was obscured by gas, lateral displacement of the colon without
nephrosplenic entrapment is more likely.36 A colonic mesenteric vessel is often
seen laterally in cases of nephrosplenic ligament entrapment (adjacent to the medial
aspect of the spleen or abdominal wall)27 due to this entrapment being often accom-
panied by a 180 rotation of the colon. False-positive and false-negative findings exist,
and diagnostic accuracy testing is complicated by the lack of a reliable reference
method in horses where the displacement resolves without laparotomy. Some horses
with other displacements of the large colon, and even LCV can have colon dorsal to
the spleen and a nonvisible left kidney chronically and without signs of coli8 (Fig. 7).
POSTOPERATIVE MONITORING
Fig. 7. Sonogram of the normal nephrosplenic area (A) with the spleen adjacent to the left
kidney. A horse with a nephrosplenic ligament entrapment of the large colon. The colon is
dorsal and lateral to the spleen and the dorsal edge of the spleen is not visible (B, yellow
arrow). A horse with a nephrosplenic entrapment where the malpositioned colonic vessel
is adjacent to the medial aspect of the spleen (C, white arrow).
the amount of fluid in the stomach seem reliable.37–39 The number of intercostal
spaces in which fluid is observed sonographically is correlated with the volume of ob-
tained reflux (r 5 0.77, P < .001) in horses with gastrointestinal disease, and the sono-
graphically estimated height of the stomach wall at the 12th intercostal space is
Fig. 8. Sonogram of a horse with septic fibrinous peritonitis depicting echoic fluid and
echoic material (fibrin) adhered to the peritoneal lining (A). Sonogram of a horse with sep-
tic peritonitis depicting echoic fluid and an adhesion between and small intestinal loop and
the peritoneal lining (B). Sonogram of a horse with peritonitis and ruptured viscus showing
a large amount of echoic fluid with large particles (C). Sonogram of a horse with septic fibri-
nous peritonitis due to gastrointestinal rupture showing hypoechoic fluid, echoic materials
(fibrin) and hyperechoic echoes of gas adhered to the fibrin (D).
Abdominal Sonographic Evaluation 207
correlated with the volume of fluid administered via nasogastric tube in normal hors-
es.38,39 In recent studies, an average of 5.7 to 7.4 L of reflux was obtained in horses
with gastric distension secondary to intestinal problems when the fluid-filled stomach
was imaged in 5 to 6 intercostal spaces.38 After administration of 6 L of fluid via naso-
gastric tube, the fluid-filled stomach was seen in 2 to 7 intercostal spaces.40 These
findings led the authors to conclude that sonography may be useful clinically to iden-
tify horses likely to have gastric reflux although the variability between horses needs
to be considered.
The intestinal wall thickness has been monitored in horses after surgical correction
of an LCV.41 In this interesting study, horses that recovered from LCV surgery without
signs of multiorgan dysfunction syndrome (MODS) had a significantly shorter period to
colon wall involution (5 mm) compared with horses diagnosed with MODS
(mean standard error 19.6 h 2.5 and 39.7 h 6.7, respectively; P 5 .006). This
is a physiologically interesting finding, informative to the understanding of clinical pro-
gression of horses in the postoperative period. However, despite differences in mean
thicknesses between groups, the overlap of individual measurements and the lack of
association with survival limit its use as a sole criterion in monitoring. Cuevas Ramos
and colleagues42 showed that horses with large or small intestinal disease that did not
need resection and anastomosis had small intestinal wall thickness and loop diameter
that normalized during the 3 days postoperatively, whereas horses with small intesti-
nal pathologic condition needing resection and anastomosis remained abnormal dur-
ing these 3 days.
Sonography may be used for an early diagnosis of incisional infections. A high sensi-
tivity (100%) and specificity (88%)43–45 have been described for this application when
discharge of the wound is used as diagnostic criteria for clinical incisional infection.
The sonographic signs in horses with septic peritonitis include corrugation of the
small and/or large intestinal walls, increased or echoic peritoneal fluid, heteroechoic
flocculent peritoneal fluid with dorsal accumulations of free gas in the case of gastro-
intestinal rupture, mesenteric lymphadenopathy and, masses or abscesses.7 It is
interesting to recognize that increased free peritoneal fluid was only found in 17 out
of 25 cases of confirmed peritonitis in a recent case series46 (Fig. 8).
SUMMARY
The use of abdominal ultrasonography provides useful diagnostic and monitoring in-
formation in the evaluation of horses with colic in the field, hospital, and postoperative
setting. Sonographic findings should be interpreted in light of clinical signs and other
diagnostic tests. During the last 4 decades, veterinarians have created a large body of
literature informative to clinicians using sonography in horses with colic. It is likely that
this technique will continue to advance in the near future as sonography becomes
more available and affordable and newer generations of veterinarians receive more
and earlier training in sonography.
DISCLOSURE
ACKNOWLEDGMENTS
The authors want to acknowledge Kari Bevevino for contributing to figures in this
article.
208 de Solis & Coleman
REFERENCES
36. Santschi EM, Slone DE Jr, Frank WM 2nd. Use of ultrasound in horses for diag-
nosis of left dorsal displacement of the large colon and monitoring its nonsurgical
correction. Vet Surg 1993;22:281–4.
37. Beder NA, Mourad AA, Aly MA. Ultrasonographic evaluation of the effects of the
administration of neostigmine and metoclopramide on duodenal, cecal, and
colonic contractility in Arabian horses: A comparative study. Vet World 2020;13:
2447–51.
38. Bankert J, Winter K, Scharner D. Vergleich zwischen sonografischen Untersu-
chungsbefunden am Magen und gewonnener Refluxmenge beim Warmblutpferd
[Comparison between gastric ultrasonography findings and the obtained reflux
amounts in warmblood horses - First results]. Tierarztl Prax Ausg G Grosstiere
Nutztiere 2019;47:366–71.
39. Lores M, Stryhn H, McDuffee L, et al. Transcutaneous ultrasonographic evalua-
tion of gastric distension with fluid in horses. Am J Vet Res 2007;68:153–7.
40. Epstein KL, Hall MD. Effect of Nasogastric Tube Placement, Manipulation, and
Fluid Administration on Transcutaneous Ultrasound Visualization and Assessment
of Stomach Position in Healthy Unfed and Fed Horses. Animals 2022;12:3433.
41. Sheats MK, Cook VL, Jones SL, et al. Use of ultrasound to evaluate outcome
following colic surgery for equine large colon volvulus. Equine Vet J 2010;42:
47–52.
42. Cuevas-Ramos G, Domenech L, Prades M. Small Intestine Ultrasound Findings
on Horses Following Exploratory Laparotomy, Can We Predict Postoperative Re-
flux? Animals (Basel) 2019;9:1106.
43. Wilson DA, Badertscher RR, Boero MJ, et al. Ultrasonographic evaluation of the
healing of ventral midline abdominal incisions in the horse. Equine Vet J 1989;
21(S7):107–10.
44. Shearer TR, Holcombe SJ, Valberg SJ. Incisional infections associated with
ventral midline celiotomy in horses. J Vet Emerg Crit Care 2020;30:136–48.
45. Protopapas A, Marr CM, Archer FJ, et al. Ultrasonographic assessment and fac-
tors associated with incisional infection and dehiscence following celiotomy in
horses. Vet Surg 2000;29:289.
46. Arndt S, Kilcoyne I, Vaughan B, et al. Clinical and diagnostic findings, treatment,
and short- and long-term survival in horses with peritonitis: 72 cases (2007-2017).
Vet Surg 2021;50:323–35.