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Intestinal Submucosa
Intestinal Submucosa
Intestinal Submucosa
Here, we describe two dogs in which canine small intestinal Standard herniorrhaphy (a simple appositional technique)
submucosa (SIS) was implanted as a biomaterial scaffold has been associated with postoperative complication rates
during perineal herniorrhaphy. Both dogs had developed ranging from 28.6% to 61%, and a recurrence rate of 10%
severe muscle weakness, unilaterally herniated rectal [3,5]. Alternative techniques have been developed to
protrusions, and heart problems with potential anesthetic improve hernial repair procedures and decrease the
risks. Areas affected by the perineal hernia (PH) located recurrence rate. Internal obturator muscle transposition
between the internal obturator and external anal sphincter (IOT) is currently the preferred surgical treatment (with
muscles were reconstructed with naïve canine SIS sheets. In recurrence rates between 2.4% and 19%), but repair can be
12 months, post-operative complications such as wound difficult, particularly if the internal obturator muscle is
infections, sciatic paralysis, rectal prolapse, or recurrence of atrophied [9,18]. Post-operative complications with the use
the hernia were not observed. Symptoms of defecatory of standard herniorrhaphy including IOT, and peripheral
tenesmus also improved. Neither case showed any signs of muscle autografts (e.g., semitendinous muscle flap or
rejection or specific immune responses as determined by superficial gluteal muscle transposition) have been
complete and differential cell counts. Our findings reported. These include sciatic nerve injury, fecal
demonstrate that canine SIS can be used as a biomaterial incontinence, infection around the incision site, prolapsed
scaffold for PH repair in dogs. rectum with excessive straining, misplacement of sutures in
Keywords: biomaterial scaffold, canine small intestinal the anal sac or rectal lumen, urinary bladder necrosis,
submucosa (canine SIS), perineal hernia urinary incontinence, and PH recurrence [1,12].
Ideally, herniorrhaphy should be easy to perform, and
repair the defect with sufficient strength to avoid recurrence
Perineal hernia (PH) results from a failure of the pelvic and minimize complications. For this, some researchers
muscle diaphragm structures to support the pelvic and have recommended the use of prosthetic implants
caudal abdominal contents (rectum, bladder, and small [synthetic polypropylene (PP) mesh] or bioscaffolds such
intestine). Consequently, these contents extend and deviate as dermal collagen sheets [8] and small intestinal
into the subcutaneous perineal region. The prevalence of submucosa (SIS) derived from pigs [19]. In the current
PH in dogs of hospital accessions is relatively low (0.1%∼ study, we prepared naïve canine SIS bioscaffolds from a
0.4%), especially among females. However, this condition donated German shepherd cadaver within 2 h of euthanasia
commonly develops in middle-aged and elderly male dogs following a previously described method [2]. This naïve
[4]. Muscle deterioration caused by PH mainly affects the graft was applied to the PH site in two dogs undergoing a
area between the external anal sphincter, the levator ani, perineal herniorrhaphy.
and coccygeal muscles [7]. This progressive shrinkage of Case 1: A 12-year-old, intact male Shih Tzu weighing 4.4
muscle fibers is possibly associated with imbalances of kg was referred to the Veterinary Teaching Hospital of
gonadal hormones, such as estrogen, androgen, and Konkuk University (Korea) with a 6-month history of rectal
relaxin, related to prostatic hypertrophy [13,17]. dyschezia, vomiting, and anorexia associated with a PH.
On presentation, the dog was alert but had a grade (III) (Fig. 2A).
heart murmur. Swelling lateral to and extending some Naïve canine SIS consisting of four-layered sheets (40 ×
distance from the right craniodorsal area to the anus was 20 mm) was inserted between the levator ani, coccygeus,
evident. The area of hernial swelling (5 × 5 × 3 cm) was and internal obturator muscles, and secured with
hard, but the site was soft and could be pushed back into the monofilament polyglyconate sutures (4-0 Maxon;
pelvic after stool was removed from the rectum. A lateral Covidien, USA) placed in a simple interrupted pattern
deviation of the rectum was detected in the herniated area (Fig. 2B). Another series of sutures (4-0 Maxon; Covidien,
by rectal examination. Ultrasonography and radiography USA) was placed in the subcutaneous tissues, and skin was
revealed a protrusion of the rectum and fatty tissue (Fig. closed with monofilament polyamide sutures (3-0 Dafilon;
1A). Differential diagnoses included rectal sacculation, B. Braun Melsungen, Germany). Castration was
rectal diverticulum, and neoplastic rectal diseases. performed because of the muscle dilation and
Therefore, magnetic resonance imaging (MRI) was weakness-related canine prostatic hyperplasia.
performed with a 3T scanner (Medinus, Korea). T1- and Buprenorphine (10 μg/kg, IM) as an analgesia was
T2-weighted images as well as T1-enhanced images were administered postoperatively every 8 h for 2 days and
obtained. Contrast agent (0.2 mL/kg, Magnevist; Bayer treatment with cephalexin (22 mg/kg) was continued twice
Schering Pharma, Germany) was intravenously injected for per day for 14 days. After surgery, a complete blood count
the T1-enhanced imaging. MRI revealed a weakness in the (CBC), differential count (DC), and serum biochemistry
perineal muscles (internal obturator, levator ani, coccygeal, profile were obtained daily for 14 days; all results were
and obturator) and an abnormally enlarged rectal dilation within normal ranges. A mild rectal protrusion from the left
between the muscles. Canine prostatic hyperplasia was side opposite to the surgical site was developed and
confirmed under the dilated rectum (Fig. 1B). identified 14 days post-operatively. This was probably due
The dog received a pre-operative intramuscular (IM) to severe rectal dilation with long-term fecal accumulation
injection of 10 μg/kg buprenorphine (Renolphan; Hanlim before surgery. We also suspected that the left side muscles
Pharm, Korea) and an intravenous (IV) injection of 0.3 to the anus in PH area were previously severely weakened
mg/kg midazolam (Vascam; HaNa Pharm, Korea). by prostatic enlargement and hormone imbalances like
General anesthesia was induced with an IV injection of 6 relaxin [13,17]. We were concerned that the canine could
mg/kg propofol (Anepol; HaNa Pharm, Korea). Inhalation have experienced anesthesia-related problems such as
anesthesia was maintained using a combination of 2% heart abnormalities and high blood pressure. Therefore, we
isoflurane (Forane; ChoongWae Pharma, Korea) and only prescribed a stool softener to prevent PH recurrence,
100% oxygen. Epidural anesthesia was induced using a and the patient did not show deviation of the rectum to the
mixture of 0.5 mg/kg bupivaccaine (Bupivacaine 0.5%; left side. Twelve months after herniorrhaphy, the dog
HaNa Pharm, Korea) and 10 μg/kg buprenorphine remained clinically normal and no complications were
(Renolphan; Hanlim Pharm, Korea). A half-circle skin reported by the owner.
incision was made over the hernia. The muscles were Case 2: An 11-year-old, castrated male Yorkshire terrier
atrophied and intermingled with omentum-like fatty tissue. weighing 3.38 kg was referred to the Veterinary Teaching
The fatty tissue was ligated and removed as necessary. The Hospital of Konkuk University (Korea) with a right-sided
herniated organs were replaced into the pelvic cavity by PH (4.9 × 4.9 × 4.8 cm), bladder/urethral calculi causing
gentle manipulation, and a clear view of the funnel-shaped defecation/urination difficulties, and clinical signs of a
tunnel between the perineal muscles was then obtained
Fig. 1. In Case 1, Positive contrast radiograph and magnetic Fig. 2. Intraoperative photographs of perineal herniorrhaphy
resonance imaging scans. (A) Lateral view showed that the using canine small intestinal submucosa (SIS) in Case 1. (A) The
rectum protruded into the hernia sac by barium enema. (B) The four-layered canine SIS sheet was prepared. After placing the
levator ani, coccygeal, and obturator muscles appeared around deviated rectum in its original location, the levator ani,
the dilated rectum, and the canine prostate was found to be coccygeus, and internal obturator muscles were identified. (B)
hyperplastic on the T1-weighted image. The canine SIS sheet was placed between the perineal muscles.
Canine SIS application in perineal hernias 329
2. Badylak SF, Lantz GC, Coffey A, Geddes LA. Small occurring after perineal herniorrhaphy in dogs. Compend
intestinal submucosa as a large diameter vascular graft in the Contin Educ Pract Vet 1989, 11, 797-802.
dog. J Surg Res 1989, 47, 74-80. 13. Niebauer GW, Shibly S, Seltenhammer M, Pirker A,
3. Bellenger CR. Perineal hernia in dogs. Aust Vet J 1980, 56, Brandt S. Relaxin of prostatic origin might be linked to
434-438. perineal hernia formation in dogs. Ann N Y Acad Sci 2005,
4. Bellenger CR, Canfield RB. Perineal hernia. In: Slatter DH 1041, 415-422.
(ed.). Textbook of Small Animal Surgery. 3rd ed. 14. Novitsky YW, Harrell AG, Cristiano JA, Paton BL,
pp.487-498, Saunders, Philadelphia, 2003. Norton HJ, Peindl RD, Kercher KW, Heniford BT.
5. Burrows CF, Harvey CE. Perineal hernia in the dog. J Comparative evaluation of adhesion formation, strength of
Small Anim Pract 1973, 14, 315-332. ingrowth, and textile properties of prosthetic meshes after
6. Clarke KM, Lantz GC, Salisbury SK, Badylak SF, Hiles long-term intra-abdominal implantation in a rabbit. J Surg
MC, Voytik SL. Intestine submucosa and polypropylene Res 2007, 140, 6-11.
mesh for abdominal wall repair in dogs. J Surg Res 1996, 60, 15. Raffan PJ. A new surgical technique for repair of perineal
107-114. hernias in the dog. J Small Anim Pract 1993, 34, 13-19.
7. Dorn AS, Cartee RE, Richardson DC. A preliminary 16. Schumpelick V, Klinge U. Prosthetic implants for hernia
comparison of perineal hernia in the dog and man. J Am repair. Br J Surg 2003, 90, 1457-1458.
Anim Hosp Assoc 1982, 18, 624-632. 17. Shahar R, Shamir MH, Niebauer GW, Johnston DE. A
8. Frankland AL. Use of porcine dermal collagen in the repair possible association between acquired nontraumatic
of perineal hernia in dogs-a preliminary report. Vet Rec inguinal and perineal hernia in adult male dogs. Can Vet J
1986, 119, 13-14. 1996, 37, 614-616.
9. Hardie EM, Kolata RJ, Earley TD, Rawlings CA, 18. Sjollema BE, van Sluijs FJ. Perineal hernia repair in the dog
Gorgacz EJ. Evaluation of internal obturator muscle by transposition of the internal obturator muscle. II.
transposition in treatment of perineal hernia in dogs. Vet Complications and results in 100 patients. Vet Q 1989, 11,
Surg 1983, 12, 69-72. 18-23.
10. Hodde JP, Badylak SF, Brightman AO, Voytik-Harbin 19. Stoll MR, Cook JL, Pope ER, Carson WL, Kreeger JM.
SL. Glycosaminoglycan content of small intestinal The use of porcine small intestinal submucosa as a
submucosa: a bioscaffold for tissue replacement. Tissue Eng biomaterial for perineal herniorrhaphy in the dog. Vet Surg
1996, 2, 209-217. 2002, 31, 379-390.
11. Kropp BP, Eppley BL, Prevel CD, Rippy MK, Harruff 20. Voytik-Harbin SL, Brightman AO, Kraine MR, Waisner
RC, Badylak SF, Adams MC, Rink RC, Keating MA. B, Badylak SF. Identification of extractable growth factors
Experimental assessment of small intestinal submucosa as a from small intestinal submucosa. J Cell Biochem 1997, 67,
bladder wall substitute. Urology 1995, 46, 396-400. 478-491.
12. Matthiesen DT. Diagnosis and management of complications