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A Cross-Sectional Study on Canine and Feline Anal Sac Disease

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Limited data are available on canine and feline non-neoplastic anal sac disease. Therefore, the aim of this study was to obtain observational data on the incidence, predisposing factors, diagnosis, treatment, and recurrence rate of canine and feline anal sac disease. To this end, a questionnaire was distributed among veterinarians. The incidence of non-neoplastic anal sac disease was estimated at 15.7% in dogs and 0.4% in cats. Predisposing factors were diarrhea, skin problems, several dog breeds, and particularly small breed dogs, male cats, British shorthairs, and obesity in dogs. Diagnosis was made based on the presence of clinical signs and characteristics of the anal sac content. Manual expression and treating any potential underlying disease were the most important treatments for all three types of non-neoplastic anal sac disease. Anal sacculectomy was performed in refractory cases. The most recurrent anal sac disease condition was impaction. Diagnosis of anal sac disease should be based on clinical signs and rectal examination, as the evaluation of the anal sac content is not reliable. Surgical outcomes of anal sacculectomy can be improved when surgery is performed after medical management. Future studies should investigate these findings in prospective trials.
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Citation: Corbee, R.J.; Woldring,
H.H.; van den Eijnde, L.M.; Wouters,
E.G.H. A Cross-Sectional Study on
Canine and Feline Anal Sac Disease.
Animals 2022,12, 95. https://
doi.org/10.3390/ani12010095
Academic Editor: Elisabetta Giudice
Received: 13 December 2021
Accepted: 30 December 2021
Published: 31 December 2021
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animals
Article
A Cross-Sectional Study on Canine and Feline Anal Sac Disease
Ronald Jan Corbee 1, * , Hilde H. Woldring 1, Lianne M. van den Eijnde 1and Erik G. H. Wouters 2
1Department of Clinical Sciences, Faculty of Veterinary Medicine, Utrecht University, Yalelaan 108,
3584 CM Utrecht, The Netherlands; hildewoldring@hotmail.com (H.H.W.);
liannevandeneijnde@hotmail.com (L.M.v.d.E.)
2AniCura Dierenziekenhuis Drechtstreek, Jan Valsterweg 26, 3315 LG Dordrecht, The Netherlands;
erik.wouters@anicura.nl
*Correspondence: r.j.corbee@uu.nl; Tel.: +31-2539411
Simple Summary:
Anal sac disease is a common problem in private practice, but there is surprisingly
little information available about anal sac disease in the literature. In this article, the incidence,
predisposing factors, diagnostics, treatment options, and recurrence rates were investigated by the
use of a questionnaire which was distributed among veterinarians in private practice. Dogs were
more commonly affected than cats. Diarrhea and skin problems increased the risk for anal sac
disease, and certain breeds were more often affected. Diagnosis was made based on the presence of
clinical signs and characteristics of the anal sac content. Manual expression and treating any potential
underlying disease were the most important treatments. Surgical removal was performed in the case
of frequent recurrence. Surgical outcome of anal sacculectomy can be improved when surgery is
performed after medical management. Future studies should investigate if these findings reported by
veterinarians can be confirmed by asking veterinarians to keep a logbook on dogs and cats with anal
sac disease.
Abstract:
Limited data are available on canine and feline non-neoplastic anal sac disease. Therefore,
the aim of this study was to obtain observational data on the incidence, predisposing factors, diagnosis,
treatment, and recurrence rate of canine and feline anal sac disease. To this end, a questionnaire was
distributed among veterinarians. The incidence of non-neoplastic anal sac disease was estimated at
15.7% in dogs and 0.4% in cats. Predisposing factors were diarrhea, skin problems, several dog breeds,
and particularly small breed dogs, male cats, British shorthairs, and obesity in dogs. Diagnosis was
made based on the presence of clinical signs and characteristics of the anal sac content. Manual
expression and treating any potential underlying disease were the most important treatments for all
three types of non-neoplastic anal sac disease. Anal sacculectomy was performed in refractory cases.
The most recurrent anal sac disease condition was impaction. Diagnosis of anal sac disease should be
based on clinical signs and rectal examination, as the evaluation of the anal sac content is not reliable.
Surgical outcomes of anal sacculectomy can be improved when surgery is performed after medical
management. Future studies should investigate these findings in prospective trials.
Keywords:
impaction; sacculectomy; dog; cat; gland; allergy; skin; diarrhea; non-neoplastic; inflammation
1. Introduction
Anal sac disease can be divided into neoplastic and non-neoplastic conditions (also
called inflammatory anal sac disease) [
1
,
2
]. The present study focusses on non-neoplastic
conditions, which can be divided into three types: impaction, inflammation, and absces-
sation [
3
,
4
]. An anal sac impaction is characterized as an enlargement of the sacs due to
retention of anal sac content, without showing any signs of inflammation except for pain
and discomfort [
3
]. The sacs are filled with thick content that can be difficult to express [
5
].
Anal sac impaction can occur unilaterally, but most often it presents itself as bilateral [
3
].
Anal sac inflammation, also called anal sacculitis, is defined as an enlargement combined
Animals 2022,12, 95. https://doi.org/10.3390/ani12010095 https://www.mdpi.com/journal/animals
Animals 2022,12, 95 2 of 12
with inflammation of the anal sac [
3
]. The anal sac and perianal region often become red,
swollen, and painful [
5
]. In the case of an anal sac abscess, pyrexia is often present; however,
pyrexia can also occur in the case of severe anal sac inflammation. Furthermore, an inflamed
and often alopecic area of the anal sacs can be observed in the case of an anal sac abscess,
again accompanied with swelling and pain. Additionally, discharge contaminated with
blood or purulent material can occur [
1
,
5
]. As an anal sac abscess progresses, the abscess
can rupture and draining fistulas can develop that may be noted on the perineum [
3
,
5
]. A
few studies determined the incidence of anal sac disease in dogs, which varied between
4.9% and 12.5% in different subpopulations [68].
The incidence of anal sac disease in cats has not been reported to the authors’ knowl-
edge, but it is stated that anal sac disease is more common in dogs compared to cats [
2
,
9
].
Several breeds have been indicated as being predisposed to anal sac disease, such as
Labrador Retrievers, German Shepherds, as well as several small breed dogs [
2
,
7
,
8
,
10
13
].
Other reported risk factors are the presence of diarrhea [
3
,
14
,
15
] as well as dermatological
conditions [15,16].
Clinical symptoms of canine anal sac disease have been investigated before and
include: “scooting”, discomfort when sitting down, licking/biting of the anal area or
tail-base region, tail chasing, tenesmus, perianal discharge, redness of the tail area, moist
dermatitis of the perianal region, and back rubbing against an object [
2
,
4
,
10
,
17
]. As other
diseases such as parasites, flea allergies, perianal tumors, perianal fistulae, and pyoderma
can cause similar symptoms [
3
,
15
], executing a rectal examination and careful palpation of
the anal sacs are very important in making a diagnosis [3,5].
The clinical signs in cats suffering from anal sac disease have, to the authors’ knowl-
edge, not yet been described in the literature, but were suggested to be similar. In the case
of anal sac disease, a visible or palpable perianal swelling at four or eight o’clock lateral to
the anus can be noted.
The distinction between anal sac impaction, inflammation, and abscessation can be
vague and the criteria on how to distinguish between these conditions differ between
studies. One study reported that the distinction must rely on history, clinical examination,
cytology, and a bacterial culture [
12
], although another study stated that the distinction can
be made by digital palpation of the anal sacs and by examining the anal sac content [13].
No randomized, controlled studies have been conducted yet on the most appropri-
ate and effective treatment for dogs with anal sac impaction, anal sac inflammation, or
anal sac abscessation. Suggested treatment options for anal sac impaction and inflamma-
tion are a combination of expressing the anal sacs, flushing the anal sacs, warm packing,
high-fiber diet, administering anti-inflammatory drugs, infusing topical antibiotics or
antibiotic-corticosteroid preparations, or prescribing systemic antibiotics [
3
,
5
,
14
,
15
]. In
addition, treatment of possible underlying factors, such as dermatological and gastroin-
testinal diseases, is recommended [
5
,
13
]. In case an abscess has developed and the therapy
is unsuccessful, an incision over the anal sac can be made, allowing for open drainage [5].
If all of the treatments are unsuccessful and the dog has recurrent anal sac disease or
in severe cases in which a fistulous tract in an abscess persists, surgical resection of the anal
sacs (anal sacculectomy) has to be considered. Several methods for anal sacculectomy have
been described, including an open method, a closed method, a modified closed method,
and a modified open method [11,18].
The prognosis for anal sac disease depends on the underlying diseases and the severity
of clinical signs. However, overall, the prognosis is variable [13].
To provide more insight into several aspects of anal sac disease and how veterinary
practitioners currently deal with this disease, the aim of this study was to obtain observa-
tional data on the incidence, predisposing factors, diagnosis, treatment, and recurrence rate
of canine and feline anal sac disease.
Animals 2022,12, 95 3 of 12
2. Materials and Methods
2.1. Questionnaire
This observational study was conducted in the form of two online open surveys (one
for each species), which were created in Qualtrics according to the Cherries Guidelines [
19
].
This study did not require evaluation by an ethical committee under Dutch legislation, as all
veterinarians that participated did so on a voluntary basis and they could withdraw from
this study at any time. We aimed at 50 participants per survey to obtain a sufficient number
of observations [
20
]. The surveys consisted of 45 multiple choice questions and descriptive
questions divided into six sections. Each page contained a maximum of six questions and
the total number of pages was ten. The surveys are available in Supplementary Material.
No randomization of items or adaptive questioning to reduce number or complexity of
the questions has been performed. Before distributing the surveys, the usability, quality, and
completeness of the questions were tested during phone calls with three independent Dutch
veterinarians. The technical functionality was tested by the investigators by previewing
the questionnaire several times. While participating in the questionnaire, there were no
mandatory items and no completeness check was performed before or after submitting the
questionnaire. However, in the introduction prior to the survey, it was highly emphasized
that for the quality of the study, it was necessary to answer all the questions completely.
Most questions provided a non-response option, such as “other, please specify
. . .
”, but
this was not the case for all the questions. If possible, selection of only one option was
enforced. Participants were able to review and change their answers during the survey
through a back button.
Since the survey was distributed by copying and pasting an anonymous link on
Facebook (closed group for Dutch veterinarians) and in e-mail messages, the responses
did not provide identifying information, such as an IP address or cookies, and multiple
responses from the same person (ballot box stuffing) were not prevented. Therefore, the
identification of unique visitors could not be determined. However, participants could
leave their e-mail address if they wished to receive the final report and this e-mail address,
together with the survey results, allowed for the identification of some unique participants.
If there were multiple responses from the same participant, only the most recent response
was kept for analysis. Some participants did not go through all of the questionnaire
pages, because participants could discontinue the survey at any time, leaving one or more
pages incomplete. However, both complete and incomplete questionnaires were collected
and therefore, each given answer was analyzed. As a result, the number of answers per
question varied.
At the first page of the questionnaire, there was informed consent. The participants
were informed about the study design, which was an observational study. Moreover,
the investigators were mentioned, as well as the institution from which this study was
carried out. In addition, the purpose of the study was explained. The length of time for
completing the survey was also stated and this was estimated to be ten to fifteen minutes.
It was emphasized that personal data would be handled with great care and that the data
would be deleted after processing. This personal information was collected and stored
in the online survey, which was protected from unauthorized access by a password and
two-factor authentication. Only the investigators had access to this.
The first section consisted of questions regarding the incidence of anal sac disease (sub-
divided into impaction, inflammation, and abscessation). In the second section, participants
were asked about predisposing factors for dogs or cats with anal sac disease, including the
gender, neuter status, age, body condition score, size, breed, coat, diet, presence of skin
disorders, and presence of gastrointestinal disorders. There were also questions concerning
whether there was an association between the type of season and the occurrence of clinical
signs and whether there was an association between the presence of diarrhea and the type
of diarrhea (small- or large-bowel diarrhea) and the occurrence of clinical signs.
In the third section, questions were asked about the diagnostics. First, the criteria used
for the diagnosis of any kind of anal sac disease were asked for. Then, questions were asked
Animals 2022,12, 95 4 of 12
on how the distinction between impaction, inflammation, or abscessation was made. In the
fourth section, participants were asked about the treatment of anal sac disease. First, the
treatment for impaction, inflammation, or abscessation in dogs was assessed.
Next, questions were asked about whether there is a difference in the treatment of
impaction, inflammation, or abscessation of the anal sacs in cats, how the decision for
anal sacculectomy is made, which method (open versus closed) is preferred, and how the
procedure is carried out. In the fifth section, questions were asked regarding the effect
of treatment, prognosis, and recurrence. In the final section, participants could give any
comments or recommendations for the survey.
2.2. Data Analysis
All responses were collected from Qualtrics
®
into Excel. The total number of responses
was recorded thereafter and empty questionnaires, in which no single answer was given,
were removed. In the end, the total number of complete and partially complete responses
was recorded. Subsequently, the questions were separated and analyzed, whereby the
number of answers for each separate question was recorded. Because both complete and
incomplete questionnaires were collected, this number varied per question.
The mean incidence of anal sac disease in the dogs and cats and the mean incidence
for each individual anal sac condition (impaction, inflammation, and abscessation) were
calculated separately based on the number of dogs or cats with anal sac disease and the
total number of dogs or cats seen by the participant. First, the answers were checked to
ascertain if they were all complete and correct. If responses were empty or if the data were
considered incorrect, they were removed from the dataset. When a range was given, the
average was included in the dataset.
Of the remaining responses, the number of dogs or cats with anal sac impaction was
added to the number of dogs or cats with anal sac inflammation and abscessation to check
if this number was equal to the total number of dogs or cats with anal sac disease. If this
number differed, a new total number of dogs or cats with anal sac disease was calculated
by adding the number of dogs or cats with anal sac impaction to the number of dogs or
cats with anal sac inflammation and anal sac abscessation.
For the average time for recurrence of anal sac disease and the average time for
recurrence of anal sac impaction, anal sac inflammation, and anal sac abscessation, the
answers were also checked to ascertain if they were complete and correct. If responses
were empty or if the data were considered incorrect, they were removed from the dataset.
When a range was given, the average was included in the dataset. If a range included “a
few months” or “a few weeks”, this was calculated as three months or three weeks.
As the generated data were only descriptive, no statistical analysis has been performed.
3. Results
3.1. Number of Surveys
For the canine survey, 69 responses were received, of which 50 (72.5%) were complete,
and 19 (27.5%) were partial responses. The feline survey had 78 responses, of which 48
(61.5%) were complete, and 30 (38.5%) were partial responses.
3.2. Incidence
The incidence of anal sac disease in dogs and cats is given in Table 1.
Animals 2022,12, 95 5 of 12
Table 1.
Incidence of anal sac disease and the subdivision between anal sac impaction, anal sac
inflammation, and anal sac abscess in dogs and cats (based on 56 and 57 responses, respectively).
Condition Incidence in Dogs Incidence in Cats
Anal sac disease 15.70% 0.38%
Anal sac impaction 8.90% 0.25%
Anal sac inflammation 4.05% 0.06%
Anal sac abscess 2.75% 0.07%
3.3. Predisposing Factors
In dogs and cats, gender, neuter status, type of coat, and diet were not regarded as
predisposing factors. Age was a factor, as anal sac disease was reported to occur more often
in adult dogs and cats compared to puppies and kittens (most of the participants reported
occurrence in adults as more common (87.7%, n= 50 in dogs, 67.8%, n= 40 in cats); the
others mentioned no difference).
Almost one-third of the participants (31.6%, n= 18 in dogs, 36.1%, n= 22 in cats)
reported that anal sac disease is more prevalent in obese animals, while a few participants
(1.8%, n= 1 in dogs, 9.8%, n= 6 in cats) reported that anal sac disease is more prevalent in
non-obese animals. However, the majority of the participants (66.7%, n= 38 in dogs, 54.1%,
n= 33 in cats) reported no difference.
Breed size distribution is given in Table 2.
Table 2. Reported predisposition to anal sac disease per breed size in dogs.
Breed Size Percentage Number of Responses
Small (<10 kg) 60.34% 35
Medium (10–30 kg) 17.24% 10
Large (>30 kg) 3.44% 2
No difference 19% 11
Dog breeds in which anal sac disease was reported the most are given in Table 3.
Table 3. Reported predisposition of anal sac disease per dog breed.
Breed Percentage Number of Responses
Chihuahua 14.53% 25
Labrador Retriever 12.79% 22
French Bulldog 11.63% 20
Jack Russell Terrier 10.46% 18
Lhasa Apso 8.14% 14
Beagle 6.40% 11
German Shepherd 5.23% 9
Boomer 4.07% 7
Cocker Spaniel 3.49% 6
Miniature Poodle 2.91% 5
Staffordshire Bull Terrier 2.91% 5
Shih Tzu 2.91% 5
Cavalier King Charles Spaniel
2.91% 5
West Highland White Terrier 1.74% 3
Springer Spaniel 1.74% 3
Maltese 1.16% 2
Labradoodle 1.16% 2
German Shorthaired Pointer 0.58% 1
No difference 5.23% 9
In cats, participants noted a higher occurrence of anal sac disease in domestic short-
hairs (37.7%, n= 23) and British shorthairs (16.4%, n= 10).
Animals 2022,12, 95 6 of 12
Anal sac disease in dogs seems to be more prevalent in spring/summer as was
mentioned by almost a quarter of the participants (25.5%, n= 13), while almost three-
quarters of participants (74.5%, n= 38) reported that there is no difference in occurrence
between spring/summer and autumn/winter. No participants reported that anal sac
disease in dogs is more common in autumn/winter. In cats, no differences in occurrence by
season were reported.
Cutaneous adverse food reactions or food allergies (37.9%, n= 39 in dogs, 20.7%,
n= 12 in cats) and atopic dermatitis (30.1%, n= 31 in dogs, 10.3%, n= 6 in cats) were
dermatological conditions mentioned as being associated with anal sac disease.
Adverse food reactions (33.7%, n= 29 in dogs, 17.9%, n= 10 in cats) and viral or bacte-
rial enteritis (25.6%, n= 22 in dogs, 10.7%, n= 6 in cats) were mentioned as gastrointestinal
diseases associated with anal sac disease. About half of the participants (48.1%, n= 26)
reported that there is a relation between the presence of diarrhea and the occurrence of
anal sac disease in dogs, but that there is no difference between small- and large-bowel
diarrhea. Almost a quarter of the participants (25.9%, n= 14) reported that there is no
difference between the presence of diarrhea and the occurrence of anal sac disease in dogs.
A minority of participants reported that there is a relation between the occurrence of small-
or large-bowel diarrhea and the presence of anal sac disease in dogs; 11.1% (n= 6) and
14.8% (n= 8) reported that anal sac disease is more prevalent in dogs with small- and
large-bowel diarrhea, respectively.
In cats, the majority of participants (70.7%, n= 41) reported no relation between the
occurrence of anal sac disease and diarrhea.
3.4. Diagnosis
Clinical signs were important for diagnosing anal sac disease (87.0%, n= 47 in dogs,
80.0%, n= 40 in cats), followed by the size of the anal sac (72.2%, n= 39 in dogs, 80.0%,
n= 40 in cats), the nature of the anal sac content (81.5%, n= 44 in dogs, 68.0%, n= 34 in
cats), the consistency of the anal sac content (74.1%, n= 40 in dogs, 66.0%, n= 33 in cats),
the presence of pain at palpation (77.8%, n= 42 in dogs, 60.0%, n= 30 in cats), the amount
of anal sac content (64.8%, n= 35 in dogs, 64.0%, n= 32 in cats), the color of the anal sac
content (66.7%, n= 36 in dogs, 54.0%, n= 27 in cats), the consistency of the anal sac (68.5%,
n= 37 in dogs, 50.0%, n= 25 in cats), the ease of emptying the anal sac (61.1%, n= 33 in
dogs, 46.0%, n= 23 in cats), the color of the anal area (40.7%, n= 22 in dogs, 22.0%, n= 11 in
cats), the smell of the anal sac content (33.3%, n= 18 in dogs, 24%, n= 12 in cats), the body
temperature (25.9%, n= 14 in dogs, 22.0%, n= 11 in cats), the shape of the anal sac (24.1%,
n= 13
in dogs, 22.0%, n= 11 in cats), the reaction on inserting the thermometer (13.0%,
n= 7
in dogs, 8.0%, n= 4 in cats), the temperature of the anal sac (9.3%, n= 5 in dogs, 2.0%,
n= 1 in cats), and microscopic examination of the anal sac content (1.9%, n= 1 in dogs,
6.0%, n= 3 in cats). Further distinction between impaction, inflammation, and abscessation
is based on the anal sac content, discomfort, and fistulation by most participants for both
dogs and cats (Supplementary Material).
3.5. Treatment
All participants treated anal sac impaction by emptying the anal sac by manual
expression (100%, n= 53) in dogs, and almost all participants (94%, n= 47) used this
treatment for anal sac impaction in cats. Treating an underlying cause was the second most
common treatment for anal sac impaction (47.2%, n= 25 in dogs, 34.0%, n= 17 in cats).
For anal sac inflammation, emptying the anal sac by manual expression was still the
main treatment (88.7%, n= 46 in dogs, 89.8%, n= 44 in cats), followed by treating an
underlying cause (50.9%, n= 27 in dogs, 40.8%, n= 20 in cats), administration of antibiotic
ointment in the anal sac (34.0%, n= 18 in dogs, 20.4%, n= 10 in cats), systemic antibiotics
(34.0%, n= 18 in dogs, 42.9%, n= 21 in cats), flushing the anal sacs (30.2%, n= 16 in dogs,
30.6%, n= 15 in cats), prescription of non-steroidal anti-inflammatory drugs (28.3%, n= 15,
Animals 2022,12, 95 7 of 12
12.2%, n= 6 in cats), and prescription of corticosteroids (18.9%, n= 10 in dogs, 0.0% n= 0 in
cats).
Abscessation was treated by prescribing a systemic antibiotic (90.6%, n= 48 in dogs,
72.0%, n= 36 in cats), manual expression of the anal sacs (56.6%, n= 30 in dogs, 70.0%,
n= 35
in cats), and flushing the anal sacs (43.4%, n= 23 in dogs, 46.0%, n= 23 in cats). Non-
steroidal anti-inflammatory drugs (28.3%, n= 15 in dogs, 14.0%, n= 7 in cats) and drainage
(11.3%, n= 6 in dogs, 14.0%, n= 7 in cats) were less frequently mentioned for treatment of
anal sac abscessation. More information on type of flush, type of antibiotic ointment, and
type of systemic antibiotic prescribed can be found in Supplementary Material.
3.6. Anal Sacculectomy
Frequent recurrence was mentioned by veterinarians as the most chosen reason to
proceed to surgical removal of the anal sacs (75.0%, n= 36 in dogs, 69.6%, n= 16 in cats).
Two different methods were used for surgical removal of anal sacs, the open and closed
method. The closed method was most often used (76.7%, n= 23 in dogs, 61.1%, n= 13 in
cats). Surgery was not performed by 38.3% of the participants (n= 18) in dogs, and by
61.7% of the participants (n= 47) in cats.
3.7. Recurrence Rate
The mean percentages of dogs with a relapse of anal sac impaction, inflammation,
or abscessation were 35.7%, 6.3%, and 2.9%, respectively. In cats, these percentages were
higher, at 40.5%, 30.1%, and 17.8%, respectively. In dogs, recurrence of anal sac impaction
and inflammation occurs on average after 4–5 months; for abscessation, the mean recurrence
time is reported to be 10 months on average. In cats, recurrence usually occurs on average
after 4–5 months for all forms of anal sac disease.
4. Discussion
The incidence of anal sac disease was higher in dogs (15.7%), compared to cats (0.4%),
which is in agreement with statements in previous studies [
2
,
9
]. This can be explained by
the difference in composition of anal sac content and location of the anal duct opening. In
dogs, the apocrine glands are more abundant compared to the sebaceous glands. Whereas
in cats, these glands are more equally distributed, in location as well as in number. Seba-
ceous glands produce a more lipid secretion, which results in more lipid anal sac content.
Combined with the more lateral location of the anal duct opening in cats, this could explain
the lower incidence of anal sac disease in cats [2,14,15].
To the authors’ knowledge, this is the first study to report incidence numbers of anal
sac disease in cats. Whether the incidence numbers in this study, based on self-reported
retrospective data, are correct needs to be proven in a prospective trial in which case logs
are kept. In the present study, the most frequent anal sac disease was anal sac impaction
(8.9% in dogs, 0.2% in cats) followed by inflammation (4.1% in dogs, 0.1% in cats) and
abscessation (2.8% in dogs, 0.1% in cats). An incidence of 7.1% for anal sac impaction has
been reported in a previous study in 3884 dogs from 89 clinics, where anal sac disease was
regarded as one of the most frequently recorded disorders in primary veterinary practices
in England [
7
]). In addition, the incidence of 8.9% is also in accordance with a study in
which 8.8% (n= 49) of 559 dogs with dermatological conditions were diagnosed with anal
sac impaction [
21
]. However, the incidence of anal sac impaction is expected to be higher
in dogs with dermatological conditions, suggesting a higher overall incidence in our study.
In the present study, anal sac disease was reported to be more prevalent in adult or old
dogs (>1 year). This is similar to a previous study where the mean age of dogs with anal
sac disease was reported to be 5.6 years (
±
2.8 years), which corresponds with the response
category “adult to old dogs” in the present study, suggesting that adult dogs as well as
older dogs may be at increased risk, while anal sac disease in young dogs (<1 year) is less
common [10].
Animals 2022,12, 95 8 of 12
Based on the present study, the same can be concluded for cats, which is in agreement
with the previous findings that cats younger than one year appeared to have significantly
more watery anal sac secretions in contrast to older cats. This may contribute to the higher
occurrence of anal sac disease observed in mature cats, since watery secretions are easier to
dispose of [4].
Obesity was reported as a risk factor in both species. This is in accordance with other
studies stating that an increased body condition score is a risk factor for anal sacculitis [
22
]
or anal sac disease [
14
,
15
]. Perianal fat can lead to compression of the anal sac ducts,
resulting in retention of anal sac content [
14
,
15
]. Furthermore, obese dogs may have poor
anal sphincter muscle tone [
3
]. Anal sac disease was reported to be more common in
small dogs (<10 kg) and medium-sized dogs (between 10 and 30 kg). These findings are
in accordance with a previous study reporting the weight of dogs with anal sac disease to
be 14.0
±
10.5 kg [
10
]. This could be due to relatively small anal sac ducts that can easily
become obstructed if the anal sac content becomes more thickened [
15
], or because of poor
anal sphincter muscle tone in small breed dogs [3].
The reported breeds from the present study are comparable to breeds observed in
previous studies, most of which are small breed dogs [
7
,
10
]. As reported previously, the Chi-
huahua might be even more at risk of developing anal sac disease when compared to other
small breeds [
8
]. Although the Labrador Retriever is a large breed, this breed also seems
to be at higher risk of developing anal sac disease which was also observed in a previous
study showing that Cavalier King Charles Spaniels and Labradors or Labrador crossbreeds
were overrepresented in the dog population presented for anal sacculectomy [11].
Labradors are more often overweight or obese [
23
], which is a predisposing factor as
demonstrated earlier. In addition, the Labrador Retriever is known to be at increased risk
for developing a food allergy or sensitivity [
24
], which might be a risk for developing anal
sac disease as well, as recurrent anal sac disease has been found in dogs with dermatological
conditions including food hypersensitivity [3,13].
The German Shepherd dog might well be at increased risk for developing anal sac
disease, since the anal sacs of this breed, compared to other breeds, lie deeper in the perianal
tissues near the rectum, which could be a risk for impaction or infection [
15
]. In the present
study, 5.2% of the participants reported that anal sac disease occurs more often in the
German Shepherd.
As the Labrador Retriever, German Shepherd, and Cavalier King Charles Spaniel all
belong to the top 10 most popular dogs in the Netherlands, it is unclear whether this is a
true predisposition, just as in cats, where the domestic shorthair, which was mentioned
as the breed with the highest incidence of anal sac disease, composes by far the largest
number of feline patients in primary practice. British shorthair cats were also mentioned,
which are known for their higher incidence of obesity [25].
Season has a small influence on the incidence of anal sac disease in dogs. The in-
creased incidence of anal sac disease during the spring/summer might be explained by
the relationship between anal sac disease and canine atopic dermatitis which was also
demonstrated in the present study [3,13].
The anal sacs can be considered as part of the skin [
1
]. If the skin is affected as a
result of a cutaneous food reaction or atopic dermatitis, the skin within the anal sacs is also
affected, resulting in increased secretion of fluid, glandular hypersecretion, and subsequent
occlusion of the ductal opening and infection. In cats, the relationship with season was not
demonstrated, probably because coinciding cutaneous food reaction and atopic dermatitis
were less reported in cats.
Adverse food reaction, as well as bacterial enteritis, can result in diarrhea or soft
stool, preventing the natural expression of the anal sacs during defecation which in turn
causes prolonged retention and occlusion of the anal sacs [
17
]. Moreover, diarrhea can
cause irritation and swelling of the perineal region, which can also lead to occlusion of the
opening of the anal sac duct and impaction, inflammation, or abscessation subsequently.
However, not all dogs with soft feces or diarrhea develop anal sac disease [10].
Animals 2022,12, 95 9 of 12
In cats in the present study, dermatological and gastrointestinal diseases were less
frequently reported to be associated with anal sac disease.
According to previous studies, diagnosis of anal sac disease should be based on the
presence of clinical signs and the findings from a clinical and rectal examination [
1
,
3
]. In
the present study, diagnosis was primarily based on the presence of clinical signs in both
dogs and cats. Other diagnostics that were used, i.e., the nature of the anal sac content, the
consistency of the anal sac content, the amount of anal sac content, the color of the anal
sac content, the smell of the anal sac content, and microscopic examination of the anal sac
content, are not very reliable.
Normal anal sac secretions can be liquid or pasty, with a variation in normal color.
There can also be large numbers of leukocytes in the normal anal sac secretion. Moreover,
the type and amount of yeasts and bacteria seen in healthy dogs and cats and dogs and
cats with anal sac disease are similar [
3
,
4
,
9
,
10
,
16
,
26
]. In addition, a large population of
leukocytes or the presence of numerous bacteria in the anal sac content can also be a
normal finding. As a consequence, macroscopic characteristics, cytology, and bacteriology
cannot be used as diagnostic tools to distinguish between healthy dogs and dogs with
anal sac disease [
10
], nor to distinguish between anal sac impaction, inflammation, and
abscessation [1].
Anal sac inflammation is characterized by a swollen, red, and painful perianal area.
Additionally, in the case of anal sac inflammation, the anal sac content can contain blood [
5
].
In the case of an anal sac abscess, the sac is enlarged and the skin overlying the anal sacs will
become thin, erythematous, and edematous [
1
,
15
]. The anal sac content can be observed
as bloody/purulent in the case of an anal sac abscess, but also in the case of severe anal
sac inflammation [
5
]. Furthermore, the sacs are extremely painful in the case of an anal
abscess [5]. Pyrexia and fistulation are also indicative of an anal sac abscess.
To the authors’ knowledge, there are no clinical trials that have evaluated the effects of
treatment options for anal sac disease. Treatment options mentioned are based on clinical
experience, and are mostly in agreement with suggestions from previous studies. Anal sac
impaction can often be treated solely by manual expression of the anal sac content [
1
,
3
,
13
].
In addition, treating the underlying cause such as a skin disease or diarrhea is an important
part of the treatment [5].
Manual expression of the anal sac content is also advised in the case of anal sac
inflammation [
3
,
5
,
13
]. However, because inflammation can be more painful, sedation or
general anesthesia may be necessary. In addition, other treatments that are described
in studies may be necessary as well, depending on the severity of the condition. These
treatments include flushing the anal sacs using an antiseptic solution, warm packing of
the anal sacs, administering anti-inflammatory drugs, or applying a local antibiotic or
antibiotic-corticosteroid ointment [
1
,
5
,
13
], which is in accordance with the responses from
the participating veterinarians in the present study. Only in severe cases, for example when
pyrexia or other systemic signs are present, are systemic antibiotics indicated [3,13].
In the case of anal sac abscessation, systemic antibiotics are recommended, as well as
emptying and flushing the anal sacs and applying antibiotic ointment [
13
] and drainage [
5
].
Flushing is performed using a saline solution [
3
] or an antiseptic solution such as a com-
bination of chlorhexidine or povidone-iodine solution added to saline [
1
,
5
]. Based on
literature, chloramphenicol should be the first choice as antibiotic ointment in anal sac
disease [
27
,
28
]. Sulfadimidine, which is a sulfonamide just like sulfadiazine, is effective
in vivo
although
in vitro
the bacteria seem to be resistant. Therefore, silver sulfadiazine
may not be an appropriate choice [
27
]. In the case of systemic antibiotics, spiramycin and
metronidazole should be the first choice, followed by amoxicillin [
28
]. In cases of pyrexia
and/or pain, non-steroidal anti-inflammatory drugs or corticosteroids can be prescribed.
To prevent healthy dogs from experiencing anal sac impaction or to prevent a relapse in
previously impacted anal sacs, sometimes anal sacs are routinely expressed by a groomer or
veterinarian [
10
,
13
]. This should be performed carefully as it can also initiate irritation of the
anal sacs and surrounding tissues, which might even enhance recurrences or progression
Animals 2022,12, 95 10 of 12
to infection [
3
,
13
]. A high-fiber diet is also recommended for prevention of anal sac
disease [3,14,15].
Surgical removal of anal sacs is indicated in the case of frequent relapse of anal sac
disease despite appropriate treatment [
5
,
11
,
15
], in case there is no response to therapy, in
case a patient has a fistulous tract that persists, or in case a patient has anal sac absces-
sation that does not respond to open drainage [
1
,
3
,
5
,
29
]. The surgical method that was
preferred by most of the participants is the closed method. This was also recommended
in previous studies, which stated that an open method is significantly associated with
a higher number of complications, including contamination of the surrounding tissues
and fecal incontinence [
30
,
31
]. It is recommended to proceed to surgical removal after
the third pharmacological treatment of anal sac impaction, inflammation, or abscessation.
Current inflammation or abscessation, irrespective of time of onset of the disease, makes
anal sacculectomy more complicated.
Although recurrence rates were higher in cats compared to dogs, anal sacculectomy
was performed more frequently in dogs because veterinarians indicated that they were
less experienced in the surgical procedure in cats. Anal sac impaction has the highest
recurrence rate, with a reported time of recurrence of 4–5 months. This is in contrast with
a previous study among pet owners who reported that clinical signs recurred within a
median frequency of three weeks (ranging from one to three days to one to two months)
or a mean of 2.5 weeks after anal sac expression. The majority of the dogs (81.3%) only
stopped scooting for three weeks or less, while 18.8% of the dogs stopped scooting for only
one to three days [10].
The present study demonstrated several aspects of anal sac disease in dogs and cats,
and how it is dealt with in private practice. All the data were self-reported by veterinarians
in a retrospective view. A prospective trial should give more insight into the true incidence,
risk factors, and recurrence rates of anal sac disease in dogs and cats. Furthermore, clinical
trials should be performed to evaluate the effect of different treatment options in order to
ultimately provide evidence-based recommendations for treatment and prevention of this
common disorder in dogs (and cats).
5. Conclusions
Anal sac disease is a common disorder in dogs, and it also occurs in cats. Diagnosis
should be based on clinical signs and rectal examination, and not on the nature or con-
sistency of the anal sac content. It is important to distinguish impaction, inflammation,
and abscessation, because they require different treatment. Anal sacculectomy should be
performed after medical treatment to improve the surgical outcome. Prospective clinical
trials are needed to be able to provide evidence-based recommendations for treatment and
prevention of anal sac disease in dogs and cats.
Supplementary Materials:
The following supporting information can be downloaded at: https:
//www.mdpi.com/article/10.3390/ani12010095/s1. S1: Questionnaires, S2: Additional Results.
Author Contributions:
Conceptualization, R.J.C.; methodology, R.J.C., H.H.W. and L.M.v.d.E.; val-
idation, R.J.C.; formal analysis, R.J.C., H.H.W. and L.M.v.d.E.; investigation, R.J.C., H.H.W. and
L.M.v.d.E.; resources, R.J.C.; data curation, R.J.C., H.H.W. and L.M.v.d.E.; writing—original draft
preparation, R.J.C., H.H.W. and L.M.v.d.E.; writing—review and editing, R.J.C., H.H.W., L.M.v.d.E.,
and E.G.H.W.; supervision, R.J.C. and E.G.H.W.; project administration, R.J.C.; funding acquisition,
R.J.C. All authors have read and agreed to the published version of the manuscript.
Funding:
This research was funded by Maria Naundorf van Gorkum Fund, a named fund of the
Utrecht University Fund 2020/2021.01.
Institutional Review Board Statement: Not applicable.
Informed Consent Statement: Informed consent was obtained from all subjects involved in the study.
Data Availability Statement: All the generated data will be available upon reasonable request.
Animals 2022,12, 95 11 of 12
Acknowledgments: The authors would like to thank all the veterinarians for their participation.
Conflicts of Interest: The authors declare no conflict of interest.
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... When secretions do not empty normally, the sacs become impacted, predisposing to anal sac disease, 4 which is common in dogs. [5][6][7][8] Typical clinical signs of anal sac impaction are scooting, licking or biting of the perianal area, tenesmus and tail chasing. ...
... 12 Stool quality and diet type have been described as risk factors. 5,13 Fibre-rich diets accelerate passage and increase the volume and water-holding capacity of rectal contents; hence, they have traditionally been investigated for the management of anal sac disease, although with limited success. 4,14 In addition, supplementation with Bacillus velezensis C-3102 increases gut bacterial diversity leading to predominance of those producing metabolites that enhance fat and carbohydrate digestibility. ...
... Finally, recurrence of anal sac impaction and inflammation has been reported to occur after 2-5 months. 5,12 Therefore, longer studies with a larger number of animals would be needed to confirm these results in the long term. Furthermore, the link between anal sac microbiota, including B. velezensis C-3102 and skin health 31 also may be better described with a larger sample size analysing the anal sac and faecal microbiome. ...
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Background Anal sac impaction is common in dogs. Manual expression may be effective, yet recurrence can be problematic. To facilitate physiological emptying of the sacs, it is important to maintain bulky stool consistency. Objectives The study evaluated if supplementation with a complementary feed product formulated as a chew containing Bacillus velezensis C‐3102 and fibre sources, reduced anal sac impaction recurrence. Animals Thirty‐five client‐owned dogs with anal sac impaction were enrolled. Materials and Methods Prospective, randomised, negative controlled field clinical trial with 22 dogs receiving the chew orally for 90 consecutive days and 13 dogs with no treatment. Dogs were evaluated on Day (D) 30, 60, 90 and 120 for the presence of clinical signs of anal sac impaction and the need to empty the sacs. Any animal that required manual expression of the sacs was classified as a failure and was withdrawn from the study. Results The cumulative percentage of failures in the untreated group increased steadily from the first follow‐up visit on D30 (15%) to the last visit on D120 (61.5%). However, in the group receiving the chew the cumulative percentage of failures increased at a much slower rate and stabilised at 19% from the D90 visit (last administration day) until the end of the study on D120, with statistically significant differences (p = 0.025). Animals receiving the chew also showed reduction in clinical signs. Conclusion and Clinical Relevance The probiotic and fibre chew was a safe and effective management option for recurrent anal sac impaction in dogs.
... Anal sac disease (ASD) is common in small animal practice, with a higher prevalence in dogs than in cats [11,12]. The most common ASD is non-neoplastic (impaction, sacculitis, abscess), diagnosed in [12][13][14][15].7% of dogs [4,13,14] and in 0.4% of cats [14]. Neoplastic ASD, namely the anal sac adenocarcinoma (ASAC), accounts for approximately 2% of canine skin tumors [15][16][17]. ...
... Anal sac disease (ASD) is common in small animal practice, with a higher prevalence in dogs than in cats [11,12]. The most common ASD is non-neoplastic (impaction, sacculitis, abscess), diagnosed in [12][13][14][15].7% of dogs [4,13,14] and in 0.4% of cats [14]. Neoplastic ASD, namely the anal sac adenocarcinoma (ASAC), accounts for approximately 2% of canine skin tumors [15][16][17]. ...
... Anal sac disease (ASD) is common in small animal practice, with a higher prevalence in dogs than in cats [11,12]. The most common ASD is non-neoplastic (impaction, sacculitis, abscess), diagnosed in [12][13][14][15].7% of dogs [4,13,14] and in 0.4% of cats [14]. Neoplastic ASD, namely the anal sac adenocarcinoma (ASAC), accounts for approximately 2% of canine skin tumors [15][16][17]. ...
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Ultrasonographic evaluation of canine and feline anal sacs is a practical promising modality to identify anal sac disease. However, limited data are available about normal ultrasound morphology of the anal sacs. This study describes the ultrasound morphology of presumed normal anal sacs in a larger sample of client-owned dogs and cats. A single-institutional prospective cross-sectional descriptive study was performed, and 137 dogs and 131 cats were included. The most common ultrasound features of the evaluated anal sacs in the dorsal plane were oval shape (99.3% of dogs and 98.5% of cats) and bilaterally similar content (94.2% of dogs and 95.4% of cats), mostly hypoechoic with diffusely hyperechoic points or unformed echogenic material (42.6% of dogs and 44% of cats). Gas in the lumen of the anal sac was detected in two dogs and mineralization in one dog. There was a statistically significant positive correlation between body weight and the size of anal sacs in dogs ≤15 kg and cats and a correlation between age and the size of anal sacs in cats. This simple method provides additional clinically significant information in detecting abnormal findings in asymptomatic patients and could contribute to the early detection of anal sac disease.
... This condition could affect up to 12.5% of domestic dogs [3,6]. In the presence of bacterial infection, local or systemic antimicrobial therapy is recommended [1,3,4,7,8]. Known predisposing factors to anal sacculitis include obesity, constipation, anal laxity, and chronic diarrhea [1,3,7]. ...
... In the presence of bacterial infection, local or systemic antimicrobial therapy is recommended [1,3,4,7,8]. Known predisposing factors to anal sacculitis include obesity, constipation, anal laxity, and chronic diarrhea [1,3,7]. Several diseases have also been reported to predispose to the development of anal sacculitis, such as dysendocrinia and atopic dermatitis [3,4,7,8]. ...
... Known predisposing factors to anal sacculitis include obesity, constipation, anal laxity, and chronic diarrhea [1,3,7]. Several diseases have also been reported to predispose to the development of anal sacculitis, such as dysendocrinia and atopic dermatitis [3,4,7,8]. However, the exact etiopathogenesis of anal sacculitis remains unclear [1,9]. ...
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... Between 4.4% and 15.7% of patients seeking primary veterinary care present with nonneoplastic anal sac disorders (ASD). [1][2][3][4][5][6] These include anal sac impaction and anal sacculitis (AS), which may progress to anal sac abscessation and fistulous tract formation from the anal sacs to the skin surface. [4][5][6][7][8][9][10][11][12] There are no objective criteria available to differentiate between anal sac impaction and AS. ...
... [1][2][3][4][5][6] These include anal sac impaction and anal sacculitis (AS), which may progress to anal sac abscessation and fistulous tract formation from the anal sacs to the skin surface. [4][5][6][7][8][9][10][11][12] There are no objective criteria available to differentiate between anal sac impaction and AS. A palpable distention of one or both anal sacs, with the sacs containing secretions that are variably difficult to express, occur in both conditions. ...
... A palpable distention of one or both anal sacs, with the sacs containing secretions that are variably difficult to express, occur in both conditions. [4][5][6][7][8][9][10][11][12] However, in anal sac impaction, there is no inflammation of the anal sac walls or the surrounding tissue in contrast with AS where concurrent infection also may be present. 4,5 Based on several studies, cytological and microbiological assessment of anal sac contents cannot be used to differentiate between dogs showing clinical signs of AS and healthy dogs because a marked overlap is seen. ...
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... Primary pruritus mainly affects the posterior in FBH, whereas in FA and AD the ears, face, muzzle, ventral neck, distal limbs, paws, axillae, inguinal, and perineum are commonly affected ( Figure 5) [82,[174][175][176][177]. Atopic dogs and dogs with FA may also present with anal sac impaction, acute moist dermatitis, acral lick dermatitis, seborrhoea, hyperhidrosis, rhinitis, reverse sneezing, gastrointestinal disturbances, and sexual cycle abnormalities [178]. Alternatively, dogs with FA may have other presentations such as erythema multiforme, cutaneous vasculitis, urticaria, anaphylaxis, seizures, and behavioral changes [14,179]. ...
... Anal sac disease is common in dogs overall but is especially common in brachycephalic dogs (up to 2.62 times the odds of dolichocephalics), particularly Pugs (up to 2.23 times the odds of non-Pugs) [3,6,97,100,188]. Obesity, soft stools, intestinal disorders, changes in muscle tone, and relatively small anal sac ducts are contributing factors to disease [178]. Recurrent anal sac disease is often associated with AD or FA [14,178]. ...
... Obesity, soft stools, intestinal disorders, changes in muscle tone, and relatively small anal sac ducts are contributing factors to disease [178]. Recurrent anal sac disease is often associated with AD or FA [14,178]. Anal sac impaction may progress to sacculitis and abscess formation. ...
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Brachycephalic dogs are not only affected by brachycephalic obstructive airway syndrome (BOAS), but are also frequently referred to veterinary dermatologists for skin conditions, with English bulldogs and pugs particularly over-represented. Some skin diseases, such as skin fold dermatitis, are directly associated with the abnormal anatomic conformation of brachycephalic dogs, while for others, such as atopic dermatitis and viral pigmented plaques, there is an underlying genetic basis or a general predisposition. Anatomic alterations associated with brachycephaly, leading to fold formation of the skin and stenosis of the ear canal, together with primary immunodeficiencies described in some breeds, favor the development of pyoderma, Malassezia dermatitis, and otitis externa/media. In addition, the frequently neglected but often lifelong dermatological problems of brachycephalic dogs are an important consideration when discussing genetic and medical conditions affecting the welfare of those dogs. Here we review the current state of knowledge concerning dermatological problems in brachycephalic dogs and combine it with clinical experience in the management of these challenging disorders.
... With some commonly diagnosed anal sac abnormalities like impaction, it is likely that some of the treatment plans immediately taken after an abnormality was detected included simple tasks such as expression of the anal sac. 4,7,9 There were several limitations of this study. First was the subjective nature of the survey, as clinicians could mark findings as normal or abnormal, as well as how the findings changed the diagnostic or therapeutic plan, depending on their clinical opinion. ...
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... Most common clinical signs include impaction, sacculitis, abscess and even development of neoplasia (Corbee et al., 2021). In the study both open vs. close method were evaluated for their effectiveness at day 1, 7, 14, 21 and 28. ...
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The anal glands are paired structure in dogs which require the surgical removal in various diseased conditions . The current study was designed to compare the efficacy of open and closed method of anal sacculectomy for better outcomes in respect of post-operative complications in dogs.The study was performed on 16 adult dogs of either sex or breed with 1 to 3 years of age presented at University Outdoor Clinic which required anal sacculectomy. All the animals were categorized into two equal groups i.e. group-A and group-B. Group A underwent open anal sacculectomy and group 2 closed anal sacculectomy. To compare surgical techniques, various hemato-biochemical, physiological parameters and post-operative complications were evaluated. The data was analyzed by applying t-test using SPSS-20 version.There was a no significant difference between both groups with respect to vital signs and hematology profile. However, seroma, abscess, stricture of anal sacs, urine incontinence, wound dehiscence and fistula formation was observed more in group A of open anal sacculectomy compared to group B of closed anal sacculectomy. It was concluded that closed technique is somewhat superior in post-surgical outcomes than open sacculectomy in terms of post-operative complications.
... In many brachycephalic breeds, especially Pugs and French Bulldogs, the nails and footpads do not wear down normally, further contributing and worsening allergic pododermatitis [145,146]. Primary pruritus mainly affects the posterior in FBH, whereas in FA and AD the ears, face, muzzle, ventral neck, distal limbs, paws, axillae, inguinal and perineum are commonly affected (Figure 5) [140,[147][148][149][150]. Atopic dogs and dogs with FA may also present for anal sac impaction, acute moist dermatitis, acral lick dermatitis, seborrhoea, hyperhidrosis, rhinitis, reverse sneezing, gastrointestinal disturbances and sexual cycle abnormalities [151]. Alternatively, dogs with FA may have other presentations such as erythema multiforme, cutaneous vasculitis, urticaria, anaphylaxis, seizures and behavioural changes [15,152]. ...
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Brachycephalic dogs are not only affected by brachycephalic obstructive airway syndrome (BOAS), but also comprise up to 30% of canine patients seen by veterinary dermatologists, with English Bulldogs and Pugs particularly overrepresented. Some skin diseases are associated with the abnormal anatomic conformation of brachycephalic dogs, while for others there is a underlying genetic basis or a general predisposition. Anatomic alterations associated with brachycephaly, leading to fold formation of the skin and stenosis of the ear canal, together with primary immunodeficiencies described in some breeds, favor the development of pyoderma, Malassezia dermatitis and otitis externa/media. Frequently neglected but often lifelong dermatological problems of brachycephalic dogs are an important consideration when discussing genetic and medical conditions affecting the welfare of those dogs. Here we review the current state of knowledge concerning dermatological problems of brachycephalic dogs, and combine it with clinical experience in the management of these challenging disorders.
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Background: All clinical research benefits from transparency and validity. Transparency and validity of studies may increase by prospective registration of protocols and by publication of statistical analysis plans (SAPs) before data have been accessed to discern data-driven analyses from pre-planned analyses. Main message: Like clinical trials, recommendations for SAPs for observational studies increase the transparency and validity of findings. We appraised the applicability of recently developed guidelines for the content of SAPs for clinical trials to SAPs for observational studies. Of the 32 items recommended for a SAP for a clinical trial, 30 items (94%) were identically applicable to a SAP for our observational study. Power estimations and adjustments for multiplicity are equally important in observational studies and clinical trials as both types of studies usually address multiple hypotheses. Only two clinical trial items (6%) regarding issues of randomisation and definition of adherence to the intervention did not seem applicable to observational studies. We suggest to include one new item specifically applicable to observational studies to be addressed in a SAP, describing how adjustment for possible confounders will be handled in the analyses. Conclusion: With only few amendments, the guidelines for SAP of a clinical trial can be applied to a SAP for an observational study. We suggest SAPs should be equally required for observational studies and clinical trials to increase their transparency and validity.
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The objective of the study was to provide normal reference featuring on the canine and feline anal sacs using ultrasound, low-field magnetic resonance imaging (MRI) and radiograph contrast study in as diagnostic imaging tools. Total ten clinically normal beagle dogs and eight clinical normally cats were included. A general radiography with contrast study, ultrasonography and low-field MRI scans were performed. The visualization of anal sacs, located at distinct sites in dogs and cats, is possible with a contrast study on radiography. Most surfaces of the anal sacs tissue, occasionally appearing as a hyperechoic thin line, were surrounded by hypoechoic external sphincter muscle on ultrasonography. The normal anal sac contents of dogs and cats had variable echogenicity. Signals of anal sac contents on low-field MRI varied in cats and dogs, and contrast medium using T1-weighted images enhanced the anal sacs wall more obviously than that on ultrasonography. In conclusion, this study provides the normal features of anal sacs from dogs and cats on diagnostic imaging. Further studies including anal sac evaluation would be expected regarding disease conditions.
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The aim of this report is to describe a modified Foley catheter technique for anal sacculectomy. A standard approach used for a closed anal sacculectomy was performed. The duct of the anal sac was then freed from the surrounding tissues and ligated. The duct was transected lateral to the ligature and a purse string suture placed. The anal sac balloon catheter was inserted through the duct into the anal sac and the purse string was tightened. Once inflated, the catheter was then used as a handle to facilitate manipulation and dissection of the anal sac from surrounding tissues. This technique permits circumferential dissection of the anal sac with good visualization, accuracy, and control, especially at the medial portion of the anal sac adjacent to the rectum. This technique can be considered for application to cases of chronic anal sacculitis and small anal gland adenocarcinomas.
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Anal sacs in normal dogs tend to be empty or soft when palpated. The majority of anal sacs contain keratinocytes as well as leukocytes. Over 75% of the leukocytes are degenerate and bacteria are rarely found intracellularly. Dogs diagnosed with anal sac adenocarcinoma are presented for evaluation of a myriad of clinical signs, the most common historical complaints including perianal swelling/rectal mass and tenesmus. Other common signs associated with anal sac neoplasia include anorexia/inappetance, polyuria/polydipsia, lethargy, weight loss, urinary incontinence, constipation, and posterior weakness. Dogs with chronic anal sac disease may also show signs of a more generalized dermatitis. During physical examination of a patient with suspected anal sac disease, a rectal examination and careful palpation of the anal sacs is essential. Comparisons have been made between open and closed techniques for anal sacculectomy for the treatment of anal sacculitis/impaction/abscessation.
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Anal sac disease (ASD) can be divided into two main categories: inflammation and neoplasia. It is relatively common in dogs, with the inflammatory form having a reported prevalence of 12.5 per cent. Cases of ASD present with signs of perineal pruritus such as licking, scooting and tail base discomfort, as well as dyschezia and tenesmus. This article discusses the most common anal sac conditions seen in veterinary practice, and describes how they can be managed, both medically and surgically.
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Anal sac disease represents a frequent complaint in small animal practice, with prevalence in dogs estimated at 12%. The condition is reported most often in small breeds, and it is rare in cats. Repeated conservative management is often unsuccessful, and the clinician must then resort to anal sacculectomy to cure the disease. Similarly, surgery is an important part of the treatment for anal sac neoplasia. This article briefly reviews the different condition that may affect the anal sacs, and focuses on their surgical treatment.
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OBJECTIVES To report the complication rate for bilateral closed anal sacculectomy in the dog and to evaluate potential risk factors for the development of postoperative complications. To identify breed groups at risk of requiring anal sacculectomy.METHODSA retrospective review of medical records of dogs undergoing bilateral closed anal sacculectomy between 2003 and 2013.RESULTSSixty-two dogs were included in the study of which 32·3% developed mild and self-limiting complications including 14·5% dogs that experienced postoperative defaecatory complications. No dog developed permanent faecal incontinence. Dogs less than 15 kg bodyweight were more likely to develop postoperative complications. Dogs that used gel to distend the anal sac were more likely to have postoperative complications than those that did not. Previous abscess formation, recurrent disease and pretreatment with antibiotics had no significant effect on postoperative complication rates. Cavalier King Charles spaniels and Labrador-type dogs were over-represented within this study population.CLINICAL SIGNIFICANCEAnal sacculectomy is a safe procedure with a relatively high rate of short-term but self-limiting, minor, postoperative complications. Smaller (<15 kg) dogs are more likely to experience postoperative complications but the risk of permanent faecal incontinence is low.