Surgery of the Bovine Reproductive System and Urinary Tract

Chapter 12 Surgery of the Bovine Reproductive System and Urinary Tract




Applied Anatomy and Examination of the Reproductive Tract


The paired testes of ruminants hang vertically in the scrotum with the caput epididymidis dorsally. They are slightly flattened laterally. Testicular blood supply is via the testicular artery, a branch of the abdominal aorta. Testicular lymph drainage is to the medial iliac lymph nodes and reflects the embryonic origin of the testes caudal to the kidneys. Autonomic innervation of the testes is via the renal and caudal mesenteric plexuses.


Cryptorchidism is rare in ruminants. When defects of testicular descent occur, it is usually in the form of incomplete descent, and its subtlety may escape notice in many cases. Instead of its normal attachment to the ventral most aspect of the scrotum, ligament of the tail of the epididymis may attach to a point in the midscrotum. In this case, the testis may appear normal at first observation. When, during examination, it is forced ventrally in the scrotum, its midscrotal attachment becomes apparent as the testis rotates about this point of aberrant attachment, instead of sliding smoothly to the ventral portion of the scrotum. Bulls with this disorder should be culled: testicular thermoregulation is impaired, and spermatogenesis is rarely normal. It is also likely that the condition is inherited.


The testis is enclosed within two layers of the tunica vaginalis. The inner layer (visceral) is closely applied to the tunica albuginea of the testis. A potential space separates it from the outer (parietal) layer; this space is continuous with the peritoneal space of the abdomen, through the inguinal canal. The sulcus formed by the fold of visceral to parietal layers of tunica vaginalis is occupied by the ductus deferens if approached from the cranial aspect and is attached to the testis along the line of the epididymis if approached from the caudal side. This architecture can be exploited to make midscrotal vasectomy a simple procedure (described later in the chapter).


The testicular artery courses toward the deep inguinal ring of the inguinal canal, where it joins the spermatic cord. The latter structure consists of the testicular artery and vein, the lymphatics, nerves, and the ductus deferens. Together they pass through the inguinal canal. The testicular artery, once external to the abdomen, becomes extremely tortuous. In this area it is in close apposition to the dilated and contorted veins. This complex is known as the pampiniform plexus. It serves multiple purposes. The multiple contortions of the artery help blunt the pulsatility of arterial blood flow. (The fibrous outer surface of the testis, the tunica albuginea, is unyielding and extremely sensitive to distension, which means that arterial pulsatility within the testis would be most uncomfortable.) In addition, arterial blood is cooled by exposure to the effluent venous blood, and countercurrent exchange of steroids, especially testosterone, which is produced in the testis and is necessary in high concentrations locally for optimal testicular function. Testicular arterial blood is therefore cooler, is fortified with testicular steroids, and flows with diminished pulsatility.


The testicular artery courses on the surface of the testis in a large S-pattern before entering the parenchyme. The surface of the testis is richly supplied with blood vessels. These are sparsest on the craniolateral surface of the testis, in its upper (dorsal) half. This is of practical significance, because this is the optimal site of testicular biopsy (a procedure with a high possibility of complications caused by hemorrhage and subsequent infarction).


The cremaster muscle is a slip of the internal abdominal oblique muscle. It may contribute to testicular thermoregulation by raising and lowering the testis but the maneuver also functions as a protection mechanism.


The products of spermatogenesis leave the seminiferous tubules (spermatogenic tubules) via tubuli recti into the rete testis. The latter is located in the mediastinum testis, a structure that runs from the proximal to the distal extremity of the testis, and is visible on ultrasonography. Via a number of efferent ductules the newly produced sperm make their way to the epididymal duct at the head of the epididymis. The epididymal duct is a single duct, and multiple connections (efferent ductules) are made to it in the caput epididymis. It is not unusual for one or more of these connecting ducts to end blindly and leave a palpable pealike nodule in the head of the epididymis. If a large number end blindly, they may become large enough to obstruct neighboring, normal ducts. Escape of sperm from these ducts provokes a granulomatous reaction to the foreign material, and further functional blockage may occur. Eventually, the granuloma formation may be sufficient to cause total functional occlusion and render one (or even both) testicular-epididymal unit inoperative. This is occasionally seen in bulls or rams. It is the mechanism of infertility associated with polled goat bucks.


The epididymis is closely applied to the body of the testis. It runs along the caudomedial surface of the testis and ends in the prominent tail (cauda epididymidis). The degree of filling of the epididymal tail is a good indicator of the status of spermatogenesis and an indicator that no blockage of the epididymis exists. The ductus deferens runs medial to the epididymis of its side, enclosed in its own fold of tunica vaginalis, the mesoductus deferens.


The testes and epididymides should be turgid without being hard. Their surfaces should be smooth, and they should be freely moveable within the scrotum.


The ductus deferens enters the inguinal canal, then courses retroperitoneally, medial to the ureters and dorsal to the bladder, where its terminal 10 cm is thickened to form the ampulla of the ductus deferens before it enters the urethra. This thickening is caused by glands in the wall of the deferent duct. The paired ampullae (left and right) are contained within a fold of peritoneum, the plica genitalis, or genital fold. An embryonic remnant, the uterus masculinus, may sometimes be found between the two ampullae.


The scrotal skin is thin, and hair or wool is usually sparse on the scrotum. It is richly endowed with glands. These modifications enhance the thermoregulatory capacity of the scrotum but also make it exquisitely sensitive to insult. Scrotal dermatitis profoundly affects scrotal temperature and spermatogenesis. The tunica dartos is a layer of fibroelastic tissue and smooth muscle that, by contracting, thickens the scrotal skin and raises the testes closer to the body and, by relaxing, lowers the testes and allows the scrotal skin to become thinner. In this way it contributes to thermoregulation. The scrotum (in contrast to the testes) receives its blood supply from the external pudendal artery, and its lymphatic drainage is to the superficial inguinal lymph node. The innervation of the testes is via the genital branch of the genitofemoral nerve, which arises from the second through fourth lumbar roots.


The vesicular glands lie immediately lateral to the ampullae, dorsal to the neck of the bladder. The vesicular glands and ampullae open into the urethra dorsally near the neck of the bladder, on either side of the colliculus seminalis. Four separate openings are present. Very close to the terminations of the ampullae and vesicular glands, and closely applied to the urethra is the body of the prostate gland, which encircles the urethra near the bladder neck. The ampullae actually pass through the parenchyma of the prostate to reach the urethral lumen and open into the urethra via multiple small ducts. In the bull there is also a disseminate part of the prostate gland, which is not palpable, within the wall of the urethra.


The pelvic portion of the urethra and its surrounding thin layer of spongy tissue are covered by the urethralis muscle. At the ischial arch the spongy tissue enlarges to form the bulb of the penis and then continues along the penile urethra as the corpus spongiosum. As the urethra passes over the ischial arch, it runs between the crura of the penis. The penile crura become fused and continue as the corpus cavernosum penis. In ruminants, the corpus spongiosum and corpus cavernosum do not communicate. The ischiocavernosus muscles cover the crura of the penis, and the bulbospongiosus muscle covers the penile bulb. Both muscles are important in the mechanism of penile erection. Partially covered by the bulbospongiosus muscle are the paired bulbourethral glands. The bulb and the crura of the penis and their covering muscles constitute the root of the penis.


The accessory sex glands are palpable per rectum in bulls. The bulbourethral glands can be felt as smooth structures that protrude from under the cranial edge of the bulbospongiosus muscles. The pelvic urethra, surrounded by the urethralis muscle, is prominent in the midline of the pelvic floor. If any doubt exists, the urethralis muscle can be identified by massaging it per rectum; it will respond by contracting rhythmically. As the urethralis muscle is traced forward, a transverse ridge can be felt at its cranial-most end. This is the body of the prostate. Converging on this point, the fairly soft, pliable ampullae can be felt. The ampullae move as a pair within the genital fold and are separated by less than half an inch. They may be displaced to one or the other side by a full bladder. Also converging toward the body of the prostate are the vesicular glands. These lobulated structures project craniolaterally. In young animals they are smaller and softer than in mature bulls.


In rams, the bulbourethral glands are larger and may be palpated by inserting a finger into the rectum. Wethers that graze estrogenic pastures may develop cystic metaplasia of the bulbourethral glands, in which case they may protrude conspicuously as swellings of the perineal area.


The urethral lumen is small, despite the deceptively large diameter of the urethralis muscle. As the urethra turns over the ischial arch there is a dorsal diverticulum formed by a shelf of mucosa. This diverticulum makes urethral catheterization of the bladder virtually impossible, as the leading tip of the catheter invariably finds the diverticulum.


The ischiocavernosus and bulbospongiosus muscles do not extend beyond the fusion of the crura of the penis. The penis is readily palpated through the skin of the perineum. It extends cranially; then turns ventrally and caudally in the first loop of the sigmoid flexure and turns cranially again ventral to the penile root. This distal loop of the sigmoid flexure is also palpable through the perineal skin. Also palpable at this point are the paired retractor penis muscles. They arise from the first two or three coccygeal vertebrae, decussate around the anus, and then pass superficially through the perineal region to attach ventrally to the penis just beyond the distal loop of the sigmoid flexure.


In the resting bull, the tip of the penis lies at a level just cranial to the scrotal neck. The skin of the prepuce (lamina externa) is reflected at the preputial orifice to form the lining (lamina interna) of the preputial cavity. The lamina interna of the prepuce is attached to the penis about 12 cm from the tip of the penis. This integument (it has no glands and is not mucosa) is supported by several layers of loose connective and elastic tissue that allow extension of the penis, during which process the lamina interna comes to lie along the body of the extended penis.


In cross-section, the penis consists of the ventral urethra (dorsal in the middle of the sigmoid flexure) surrounded by the corpus spongiosum and the larger corpus cavernosum (the fusion of the crura of the penis). The corpus cavernosum is encased in a thick, dense, and inelastic tunica albuginea. The corpus cavernosum is supplied by the deep artery of the penis and is drained by the analogous vein. The artery of the bulb of the penis supplies the corpus spongiosum. The dorsal artery of the penis supplies the superficial structures of the penis. The deep artery of the penis, the artery of the bulb and the dorsal artery of the penis are terminal branches of the internal pudendal artery.


The penis of mature bulls is about 120 cm in length, with some breed variation, and extends 30 to 50 cm from the prepuce when erect. Near the free end of the penis is a dorsally located thickened fibrous band, termed the apical ligament. This ligament helps hold the penis straight for intromission. At ejaculation it slips to the side and causes a spiral deviation of the tip of the penis. In some bulls, the ligament slips prematurely, and the spiral deviation arises before intromission, making intromission impossible. The penis of the ram and buck is characterized by a urethral process that extends 4 to 5 cm beyond the glans penis.


The pudendal nerve arises from ventral branches of the second through fourth sacral spinal nerves. Its branches provide motor supply to the retractor penis muscle and, via the dorsal nerve of the penis, sensory innervation of the penis. Penile sensation is important for normal function. Afferent impulses from the glans penis, conducted by the dorsal penile nerve, are essential for ejaculation. Bulls that have lost penile sensation are unable to serve and ejaculate, even if an artificial vagina is used. Care must be taken during surgical procedures to avoid damage to the dorsal nerve of the penis. Fortunately, the nerve divides into plentiful terminal branches near the free end of the penis, and the risk of damage to the entire nerve in this area is small.


Blocking the pudendal nerve achieves relaxation and desensitization of the penis and allows surgical procedures on the penis of the standing, restrained bull, provided the animal’s temperament permits. The pudendal nerve can be palpated per rectum. The internal pudendal artery serves as a landmark. It is readily palpable (per rectum) as it courses along the medial surface of the sacrosciatic ligament just dorsal to the ischiatic arch. If the artery is followed caudally, the lesser ischiatic foramen can be identified at the point where the artery divides. The pudendal nerve can be felt about 1 cm dorsal to the artery at the cranial edge of the lesser ischiatic foramen. It is convenient to block the nerve at the foramen and remember that it receives a branch from the caudal cutaneous femoral nerve at that point. The caudal cutaneous femoral nerve runs laterally to the sacrosciatic ligament. To administer a pudendal nerve block, the rectum is evacuated and the skin of the ischiorectal fossa disinfected. A bleb of local anesthetic agent (e.g., 2% lidocaine) is injected under the skin at the notch between the tail fold and the caudal extent of the sacrosciatic ligament, and a 15-cm, 18-gauge needle is inserted. The needle is guided toward the lesser ischiatic foramen with a hand in the rectum and the left hand is used to guide the needle for injection of the right nerve, and vice versa. The author prefers to inject about 10 to 12 ml at the site of the foramen, near the palpable pudendal nerve, and then divert the needle through the foramen to inject about 5 ml on the lateral side of the ligament, thus ensuring that the caudal cutaneous femoral branch is blocked. As the needle is withdrawn, the remaining 3 to 5 ml is injected slowly, in the hope of blocking the caudal rectal nerve. This nerve, although large, is not readily palpable per rectum because it moves with the rectal wall. It provides some innervation to the proximal fibers of the retractor penis muscle. Both pudendal nerves need to be blocked to produce relaxation of the retractor penis muscles and analgesia of the penis. The penis may prolapse out of the prepuce spontaneously after this procedure, but more commonly it is retained within the prepuce by passive mechanisms (loose connective and elastic tissue surrounding the prepuce), and it needs to be extended manually.


The flaccid and insensitive penis should be extended fully, by grasping the free end of the penis with a gauze swab (see Figure 12.1.5-5). Forceps may be used to secure the penis, with care taken not to penetrate the tunica albuginea (see Figure 12.1.5-3B). Penetrating towel clamps may be secured to the apical ligament without injury to the penis.




The length of the fully extended penis should be measured from the natural position of the preputial ostium to the tip of the extended penis. For adult bulls of most breeds, this length should exceed 30 cm. An unusually short penis may prevent normal mating, especially in bulls older than 3 or 4 years. Penis extension may be impeded by lesions of the retractor penis muscles (congenital shortness, fibrosis, and calcification). These can be detected by palpating the retractor penis muscles, between the scrotum and the anus, while tension is applied to the tip of the extended penis. Some bulls may be restored to service by myotomy of the retractor penis muscles, performed in the mid to upper escutcheon.


While the penis is extended—and in particular if any impediment to full extension is encountered—the entire penis should be carefully palpated, with particular attention paid to the presence of swellings or adhesions surrounding the penis. The preputial cavity may be examined in more detail by inflating it with gas or fluid. A metal or plastic catheter with rounded tip is inserted into the preputial orifice, and through it compressed air or water (from a regular hose pipe) is carefully introduced, while the preputial orifice is held closed. The normal prepuce is clearly outlined by this procedure and should appear symmetrical and oval in contour. This technique will reveal any irregularity of the preputial lining (scars or adhesions) that may not otherwise be readily detectable.


Another strategy for minor procedures or examination of the free end of the penis is to block the dorsal nerve of the penis. This is especially useful in younger bulls, which are more easily handled. To block the dorsal nerve of the penis, the penis is withdrawn from the prepuce by manual, hand-over-hand action. Working from the left-hand side of the bull, the penis is grasped through the skin of the prepuce and moved forward with the right hand. Then the preputial skin is moved caudally and the penis is anchored with the left hand. With the right hand, the preputial skin is moved caudally, the penis is grasped again and moved forward. (It might be possible to push the penis forward by applying pressure at the distal loop of the sigmoid flexure.) This procedure is repeated until the tip of the penis protrudes from the preputial orifice, where it is grasped by an assistant with sterile gauze sponges. This is only feasible in young (yearling) bulls; the force of the retractor penis muscles is not easily overcome in more mature bulls. Once the penis is extended, lidocaine may be injected beneath the lamina interna of the prepuce dorsally near the preputial orifice. The injection should encompass the dorsal half of the penis. This will provide analgesia of the free part of the penis adequate for minor surgery such as removal of fibropapillomata, correction of persistent frenula, or for more detailed examination.


The preputial orifice should be closely applied to the ventral midline of the bull. Some breeds or individuals have pendulous prepuces that are predisposed to prolapse of the lamina interna. The orifice should permit introduction of three or four fingers but should not be wider than that. The prolapsed lamina interna is predisposed to injury, which may result in local scar tissue formation and stenosis of the prepuce. These lesions can usually be palpated through the skin. If doubt exists, the prepuce of the sedated bull can be inflated by introducing water or compressed air slowly into the prepuce while holding the orifice shut by hand. As the preputial cavity becomes filled its contour is readily discernable, and any stenotic area is easily identified.


Although the surgeon is principally concerned with the structural integrity of the reproductive tract and its surgical restoration, any surgery of the reproductive tract should, wherever possible, be preceded by thorough breeding soundness examination, including assessment of semen quality, to preclude other, nonsurgical problems that would persist after surgical intervention.



Castration



BILATERAL ORCHIDECTOMY


Castration of young ruminants is a common procedure often done by lay people to improve meat quality and render males more manageable. It is appropriate for veterinarians to educate their livestock owners to minimize complications from this procedure. A clean, dry environment as well as fly control is encouraged to prevent postoperative infection.


The desired age at which the animal is castrated varies and depends on an owner’s expectation, ease of pro-cedure, and the intended use of the animal. Younger animals are easier to restrain, have a lesser risk of incisional complications, and have decreased aggressive behavior after castration. However, some livestock owners feel that castration at a later age is preferable for improved carcass characteristics and weight gain. In a review of the literature, castration had a mixed effect on weight gain of cattle.


Castration can be done pharmacologically by using immunization against GnRH or by insertion of an estrogen implant. Other techniques include using surgical and bloodless castration techniques. This chapter will focus on the latter two methods of castration.


All small ruminants that are castrated should receive a tetanus prophylaxis (ideally several weeks before the procedure) because tetanus acquisition is one of the main complications of this procedure. This can be in the form of colostral protection, tetanus antitoxin (250 to 500 IU) or two doses of tetanus toxoid (first one 3 to 4 weeks in advance of procedure).


Regardless of the technique used or species involved, it is essential to check that both testes have descended into the scrotum before surgery is contemplated. This prevents unilateral castration of cryptorchid animals, which would give the misleading external appearance of a castrated male. Fortunately, cryptorchidism is rare in calves, rams, and bucks.



CASTRATION OF CALVES AND SMALL RUMINANTS


Lambs and small goats are held, head down, between the operator’s knees or head up with the front and hind limbs on each side held together. Calves younger than one month of age are usually restrained in lateral recumbency. Typically, older calves are put into a squeeze chute or stocks. Many operators elect to use a local anesthetic in the skin and/or spermatic cord, although some young calves and lambs receive operations with only physical restraint. For a standing animal in stocks or head catch, the operator’s hand is placed at the base of the tail so that it can be lifted over the animal’s back. Lamb or kid sensitivity to local anesthetics necessitates reduction of the concentration of a local anesthetic being administered; lidocaine should be diluted from 2% to 0.5% or 1%. General anesthesia—or heavy sedation (xylazine hydrochloride 0.02 to 0.1 mg/kg IV or 0.04 to 0.2 mg/kg IM) and local anesthesia—are commonly used with larger animals and pets. The lower range should be used on goats and debilitated, aged, young, or depressed animals. Another drug combination that works well on goats is midazolam (0.1 to 0.2 mg/kg IV) in combination with butorphanol (0.02 mg/kg IV).


For animals less than 150 kg, the distal portion of the scrotum is grasped and pulled distally, thus displacing the testes proximally (Figure 12.1.1-1). The distal third of the scrotum is excised to expose the testes (Figure 12.1.1-2). Traction is applied to each testis, and the spermatic cord is freed by stripping the fascia proximally (Figure 12.1.1-3). At this point, the cord can be ligated and transected, emasculated, or stretched until the vasculature ruptures. The latter technique results in vasospasm, which is usually adequate hemostasis for smaller animals but could damage the inguinal ring in lambs and lead to a hernia. For this reason, use of a technique that closes (use of emasculator [Figure 12.1.1-4] or ligation) the spermatic cord is preferable. The wound is usually left open to heal by second intention.






Another surgical option for calves is to approach the testes by making a vertical incision in the lateral wall of the scrotum with a Newberry knife (Figure 4.4-6A). The Newberry knife blade is placed through the middle of the scrotum (Figure 4.4-6A) and rapidly pulled distally, thus making a cranial and caudal flap of the scrotal skin (Figure 4.4-6A). The same flaps can also be created with a scalpel. The testes are excised as mentioned previously, either with traction, an emasculator, or ligation and excision. The wound is typically left open.


Older animals are occasionally castrated, with the best results obtained when they are restrained in chutes or on a tilt table. Local anesthetic in the scrotal skin and spermatic cord is appropriate. The operator’s preferences dictate the surgical approach. The distal scrotum can be removed (Figure 12.1.1-5), or vertical incisions can be made on either side of the median raphe. Regardless, the testis is identified and freed from its surrounding fascia with blunt dissection. Once isolated, the spermatic cord is ligated and transected or emasculated. Generally, the vaginal tunic is not incised and is removed en bloc with the testis. If the vaginal tunic is incised, the testis and spermatic cord are ligated (or emasculated). Some prefer to split the spermatic vessels away from the pampiniform plexus and ligate (or emasculate) these structures separately. Regardless, the cremaster muscle is ligated with the vaginal tunic, and both are transected approximately 2 cm distal to the ligations. Transfixation sutures help prevent ligature slippage. If primary closure is to be performed, at least a partial resection of the redundant scrotal skin is necessary to minimize dead space. The subcutaneous tissues are closed with a pursestring-type suture (superficial and deep bites) using an absorbable suture material. A subcuticular or skin closure should be done with an absorbable suture if primary closure is elected.




UNILATERAL ORCHIDECTOMY


Injury or illness that involves one testis may detrimentally affect the contralateral tests to the extent that removal of the affected testis provides the best option for returning the bull or ram to fertility. This may be the case in unilateral hydrocele, hematocele, testicular tumor, epididymitis, abscess, varicocele (Figure 12.1.1-6A) or other conditions. In such cases the contralateral testis may be compromised by pressure or increased local temperature. Careful removal of one testis results in preservation of the remaining testis, and some compensatory hypertrophy and increased sperm production by the remaining testis may be expected.



Abnormalities are usually detected during physical and routine breeding soundness examination or may be noticed by an astute owner or herdsman. The abnormality can involve the scrotum, testis, epididymis, ductus deferens, vaginal tunic, or vasculature of the testis. Unilateral disease can result in abnormal semen quality as the heat generated by the abnormal testis affects the contralateral testis. Fortunately, studies have shown the effect on semen quality is reversed after the abnormal testis is removed. Care must be taken to limit postsurgical hemorrhage and inflammation and to prevent the detrimental effects of postoperative pressure or elevated temperature on the remaining testis.


The surgical procedure for unilateral orchidectomy is as follows. The animal is restrained or anesthetized in lateral recumbency. The upper hind limb is abducted and secured in a fixed position; the scrotum may be held by a towel clamp to facilitate preparation (Figure 12.1.1-6B). After preparation of the surgical site, a vertical incision is made on the lateral aspect of the affected side approximately the entire length of the testis. The initial dissection extends the skin incision through the scrotal fascia, and the testis is bluntly dissected within the vaginal tunic. The vaginal tunic is incised the length of the testis, and the spermatic cord isolated, double-ligated, and transected or emasculated. The tunic can be transected and oversewn with an absorbable suture material. It is usually necessary to remove excess scrotal skin. This will help minimize dead space and prevent postoperative seroma formation. The scrotal fascia is closed by using a continuous pattern with an absorbable suture. The subcutaneous tissues and skin are closed routinely. Studies have shown that semen quality returned to normal 22 days after unilateral castration in normal bulls. There are other case reports of successful return to production following surgery in several animals with unilateral disease. Currently, surgery is recommended for valuable animals with nonheritable unilateral disorders other than herniation.



BLOODLESS CASTRATION


Several techniques for castrating farm animals without performing a surgical incision are available. These so-called “bloodless techniques” create ischemia of the testis with subsequent atrophy or necrosis. In very young animals, the most common technique is to use an elastic band. The band and applicator pliers should be soaked in disinfectant before use. Once the animal is restrained, the band is applied around the neck of the scrotum by using the pliers (Figure 12.1.1-7A and B). Other commercially available tools are designed to place heavy-walled latex tubing around the neck of the scrotum in older animals. The scrotum and testes usually slough within 3 weeks of band application. This technique is used quite commonly in small ruminants less than one month of age. Ambulatory clinicians at our institution have been successful with using a callicrate bander* in bulls up to 400 kg (Figure 12.1.1-8). Rare failure has been associated with band breakage. Older, small ruminants should be handled the same as older calves with sedation and surgery; however, one should always be mindful of small ruminant sensitivity to lidocaine. The callicrate bander has been used successfully on older goats after the long hair was clipped from the neck of the scrotum.




Another bloodless technique is to use a Burdizzo emasculatome (Figure 12.1.1-9) to crush the spermatic cord within the scrotum. After this, the testes atrophy but usually do not slough. This instrument is best used by crushing a portion of the scrotum while holding the spermatic cord over the side that is crushed. One can crush the spermatic cord twice while manipulating the cord within the scrotum. These crushes should be staggered without crossing the midline; so no pressure is applied across the entire scrotum, thus minimizing the risk of impairing vascular supply. All animals treated with nonsurgical castration techniques should receive tetanus prophylaxis (ideally several weeks before the procedure) because tetanus acquisition is one of the complications of this procedure.






12.1.2 Testicular Biopsy


Robert O. Gilbert and Susan L. Fubini


Recently, testicular biopsy was performed on six normal bulls to determine whether this would be a useful diagnostic tool for bulls with infertility. The investigators used a 15.2-cm 14-gauge biopsy needle placed through a stab incision in the skin. They determined that there were no long-term changes in semen quality over the course of the 90-day study. Therefore testicular biopsy with histopathological examination may be considered for cases of infertility if time and economic constraints preclude a wait-and-see approach for determining the future breeding ability of a particular bull. It is important to obtain the tissue sample from the lateral cranial aspect of the proximal (dorsal) area of the testis where blood vessels are relatively sparse to prevent excessive hemorrhage and infarction. Severe hemorrhage may necessitate removal of the testis (Figure 12.1.2-1). Cultures and sensitivity should be used to assess a testicular condition associated with an inflammatory or infectious process.


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Sep 3, 2016 | Posted by in SUGERY, ORTHOPEDICS & ANESTHESIA | Comments Off on Surgery of the Bovine Reproductive System and Urinary Tract

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