4: Diagnostic and Therapeutic Procedures

Section 4 Diagnostic and Therapeutic Procedures





Routine procedures



Administration techniques for medications and fluids



Oral Administration: Tablets and Capsules—Canine





Technique

The simplest method of administering tablets or capsules to dogs is to hide the medication as bait in food. Offer small portions of unbaited cheese, meat, or some favorite food to the dog initially. Then offer one portion that includes the medication. Pill Pockets Canine Treats* is a commercially available alternative.



For anorexic dogs or when pills must be given without food, give medications quickly and decisively so that the process of administering the medication is accomplished before the dog realizes what has happened. With cooperative dogs, insert the thumb of one hand through the interdental space, and gently touch the hard palate. This will induce the cooperative dog to open its mouth (Figure 4-1). Using the opposite hand (the one holding the medication), gently press down on the mandible to open the mouth further (Figure 4-2). Quickly place the tablet or capsule onto the caudal aspect of the tongue. Quickly withdraw the hand and close the dog’s mouth. When the dog licks its nose, the medication likely has been swallowed.




Dogs that offer more resistance can be induced to open their mouths by compressing their upper lips against their teeth. As they open the mouth, roll their lips medially so that if they attempt to close the mouth, they will pinch their own lips. Alternatively, dripping water onto the nostrils or blowing into the patient’s nose sometimes encourages the patient to accept and swallow oral medications (tablets or capsules). Pilling syringes are also available and in some dogs seem to work well.




Oral Administration: Tablets and Capsules—Feline




Technique


Caution: Only experienced individuals should attempt this technique of administering tablets or capsules to cats. Even cooperative cats that become intolerant will bite. Therefore, this is not a technique recommended for most owners to try at home, even if specific instructions have been given.


Two methods of pill administration are used in cats. In both methods the cat’s head is elevated slightly with the nose pointed upward. Success in administering pills and tablets to a cat entails a delicate balance between what works well and what works safely. In cooperative cats, it may be possible to use one hand to hold and position the head (Figure 4-3) while using the opposite hand (the one holding the medication) to open the mouth gently by depressing the proximal aspect of the mandible (Figure 4-4). Press the skin adjacent to the maxillary teeth gently between the teeth as the mouth opens, thereby discouraging the cat from closing its mouth. With the mouth open, drop (do not push) the medication (try generously lubricating the tablet or capsule with butter) into the oral cavity. The cat can be tapped under the jaw or on the tip of the nose to facilitate swallowing if you really think this works. If the cat licks, administration was probably successful.




Alternatively, some cats will tolerate a specially designed “pilling syringe” in an attempt to administer a tablet or capsule. The pilling syringe works well as long as it is inserted cautiously and atraumatically into the cat’s mouth. However, if resistance ensues, the rigid pilling syringe may injure the hard palate during the ensuing struggle. Subsequent attempts to use the syringe may be met with increasing resistance and increasing risk of injury. Success with a pilling syringe depends largely on the cat. Pill Pockets Treats are also available for use in cats and are manufactured in chicken and fish flavors. In addition, as is the case in dogs, some cats will respond to the application of water drops on the nostrils or blowing into the nostrils to encourage swallowing.




Oral Administration: Liquids



Without a Stomach Tube






With an Administration Tube




Technique

Administration of medications, contrast material, and rehydrating fluids can be accomplished with the use of a well lubricated feeding tube passed through the nostrils into the stomach or distal esophagus. When a feeding tube is placed for long-term use (multiple days) and repeated use (described under Gastrointestinal Procedures later), it is generally recommended to avoid passing the tip of the tube beyond the distal esophagus. The reason for recommending nasoesophageal intubation over nasogastric intubation is based on the fact that reflex peristalsis of the esophagus against a tube passing through the cardia can result in significant mucosal ulceration within 72 hours. This is not a factor in patients receiving a single dose of medication or contrast material.


The narrow lumen of tubes passed through the nostril of small dogs and cats limits the viscosity of solutions that can be administered through a tube directly into the gastrointestinal tract. Nasoesophageal intubation can be done with a variety of tube types and sizes (Table 4-1). Newer polyurethane tubes, when coated with a lidocaine lubricating jelly, are nonirritating and may be left in place with the tip at the level of the distal esophagus. When placing the nasogastric tube, instill 4 to 5 drops of 0.5% proparacaine in the nostril of the cat or small dog; 0.5 to 1.0 mL of 2% lidocaine instilled into the nostril of a larger-breed dog may be required to achieve the level of topical anesthesia needed to pass a tube through the nostril. With the head elevated, direct the tube dorsomedially toward the alar fold (Figure 4-6). Pushing dorsally on the nasal philtrum and pushing the nostril from lateral to medially will help facilitate passage of the tube into the ventromedial nasal meatus.


Table 4-1 The French Catheter Scale Equivalents*














































































































  Size
Scale Millimeters Inches
3 1 0.039
4 1.35 0.053
5 1.67 0.066
6 2 0.079
7 2.3 0.092
8 2.7 0.105
9 3 0.118
10 3.3 0.131
11 3.7 0.144
12 4 0.158
13 4.3 0.170
14 4.7 0.184
15 5 0.197
16 5.3 0.210
17 5.7 0.223
18 6 0.236
19 6.3 0.249
20 6.7 0.263
22 7.3 0.288
24 8 0.315
26 8.7 0.341
28 9.3 0.367
30 10 0.393
32 10.7 0.419
34 11.3 0.445

* Multiple types of pediatric polyurethane nasogastric feeding tubes are available in sizes ranging from 8F to 12F that easily accommodate administration of liquids medications and fluids to kittens, cats, and small dogs.



Caution: The tip of the feeding tube can be inadvertently introduced through the glottis and into the trachea. Topical anesthetic instilled into the nose can anesthetize the arytenoid cartilages, thereby blocking a cough or gag reflex.


After inserting the tip 1 to 2 cm into the nostril, continue to advance the tube until it reaches the desired length. If the turbinates obstruct the passage of the tube, withdraw the tube by a few centimeters. Then readvance the tube, taking care to direct the tube ventrally through the nasal cavity. Occasionally it will be necessary to withdraw the tube completely from the nostril and repeat the procedure. In particularly small patients or patients with obstructive lesions (e.g., tumor) in the nasal cavity, it may not be possible to pass a tube. Do not force the tube against significant resistance through the nostril.


Gavage, or gastric lavage and feeding, in puppies and kittens can be accomplished by passing a soft rubber catheter or feeding tube into the mouth, tilting the puppy’s or kitten’s head, and watching it swallow the tube. Most puppies or kittens will struggle and vocalize. They usually will not vocalize if the tube has been placed into the trachea. A 12F catheter is of an adequate diameter to pass freely, but it is too large for dogs and cats less than 2 to 3 weeks of age. Mark the tube with tape or a pen at a point equal to the distance from the mouth to the last rib. Merely push the tube into the pharynx and down the esophagus to the caudal thoracic level (into the stomach). Verify the placement of the tube using the same dry syringe aspiration technique to ensure that the tube is positioned in the esophagus or stomach rather than the trachea. Attach a syringe to the flared end, and slowly inject medication or food.


Depending on the feeding tube type, the end of the tube may or may not accommodate a syringe. For example, soft, rubber urinary catheters are excellent tubes for single administration use. However, the flared end may not accommodate a syringe. To affix a syringe to the outside end of a tapered feeding tube or catheter, insert a plastic adapter (Figure 4-7) into the open end of the tube.





Topical Administration





Nasal






Dermatologic



Patient Preparation

Several objectives should be considered when treating dermatologic disorders with topical medication: (1) eradication of causative agents; (2) alleviation of symptoms, such as reduction of inflammation; (3) cleansing and debridement; (4) protection; (5) restoration of hydration; and (6) reduction of scaling and callus. Many different forms of skin medications are available, but the vehicle in which they are applied is a critical factor (Box 4-1).







Subcutaneous Injection




Technique

Dogs and cats have abundant loose alveolar tissue and easily can accommodate large volumes of material in this subcutaneous space. The dorsal neck is seldom used for subcutaneous injections because the skin is somewhat more sensitive, causing some patients to move abruptly during administration. A wide surface area of skin and subcutaneous tissue over the dorsum from the shoulders to the lumbar region makes an ideal site for subcutaneous injections.


Administration of drugs, vaccines, and fluids by the subcutaneous route represents the most commonly used route of parenteral administration in dogs and cats. For small volumes (<2 mL total), such as vaccines, a 22- to 25-gauge needle generally is used. The site most often used is the wide area of skin over the shoulders. The large subcutaneous space and the relative lack of sensitivity of skin at this location make it an ideal injection site. Cleaning of the skin with alcohol or other disinfectant generally is performed before injection. Several injection techniques are used. A common technique entails grasping a fold of skin with two fingers and the thumb of one hand. Gently lift the skin upward. Using the opposite hand, place the needle, with syringe attached, through the skin at a point below the opposite thumb. Aspiration before injection is not typically necessary when using this route of administration. After administration and on removal of the needle from the skin, gently pinch the injection site and hold it for a few seconds to prevent backflow of medication or vaccine onto the skin.


When larger volumes are to be administered—fluids in dehydrated dogs and cats—the skin directly over the shoulders is the injection site most commonly selected. Generally, only isotonic fluids are administered by the subcutaneous route. Depending on the patient’s size, needles ranging from 16 to 22 gauge can be used. Because of the larger volumes of fluid involved, warming of the fluids before administration is recommended. Doing so can enhance significantly the patient’s tolerance for the displacement of skin during the period of administration and, in small patients, prevent hypothermia.


Depending on the rate of administration and breed of dog, relatively large volumes of fluid generally can be given in one location. Cats typically tolerate 10 to 20 mL/kg body mass in a single location. Large dogs can tolerate volumes greater than 200 mL of fluid in a single location. When administering large volumes, it is usually not necessary to use multiple injection sites for purposes of distributing the total fluid volume. Doing so actually may increase the risk of introducing cutaneous bacteria under the skin. Because the administration time required to deliver larger volumes is longer, and the injection needle will be placed in the skin for extended periods, it is appropriate to cleanse and rinse the skin carefully before actually inserting the needle. Isotonic, warmed fluids may be administered by large syringe or through an administration tube attached to a bag. Monitor skin tension and the patient’s comfort tolerance throughout the procedure.


Although fluid absorption begins almost immediately on subcutaneous administration of fluids, significant pressure caused by the bolus of fluid delivered can develop within the fluid pocket. On removal of the needle, firmly grasp the injection site with the thumb and forefinger for several seconds. The procedure is not complete until one has verified that back-leakage of fluid from the subcutaneous space onto the skin is not occurring. Depending on the patient’s hydration status and physical condition, fluid absorption may take from 6 to 8 hours.





Implanted Subcutaneous Fluid Ports



Technique

Recently, implantable subcutaneous ports* have been introduced for use in patients requiring regular administration of subcutaneous fluids at home. A 9-inch silicon tube is preplaced under the skin and is sutured in place by a veterinarian. Objectively, this offers easy access to the subcutaneous space without the need for needle penetration. Owners simply attach a syringe or extension tube tip to the port and administer the appropriate volume of fluids at an appropriate rate and frequency.






Transdermal (Needle-Free) Administration




Technique


Intradermal administration of vaccine and drugs in veterinary and human medicine largely has been limited to the complexities of accurately delivering the desired dose into, and not under, the skin. In 2004 a transdermal administration system* was introduced for cats (recombinant feline leukemia virus [FeLV] vaccine) that was designed after a similar device used in human (pediatric) medicine. Recently the transdermal administration system used for administration of the recombinant FeLV vaccine has been re-designed. This same administration system is now used for the transdermal administration of the oral melanoma vaccine. The transdermal administration system consistently delivers a precise volume of vaccine into the skin, subcutaneous tissues, and muscle. Use of the transdermal administration system should only be used to administer those vaccines approved for this method of delivery.






Additional Reading


Crow S, Walshaw S: Manual of clinical procedures in the dog, cat, and rabbit, ed 2, Philadelphia, 1997, Lippincott-Raven.


Kirby R, Rudloff E: Crystalloid and colloid fluid therapy. In Ettinger SJ, Feldman EC, editors: Textbook of veterinary internal medicine, ed 6, St Louis, 2005, Elsevier.


Marks S: The principles and practical application of enteral nutrition, Vet Clin North Am Small Anim Pract 28:677, 1998.


Wingfield WE: Veterinary emergency medicine secrets, Philadelphia, 1997, Hanley & Belfus.




Blood pressure measurement: indirect




Technique


Generally, two techniques are used. Oscillometric blood pressure (BP) measurement entails use of an automated recording system. A cuff is applied to the base of the tail or a distal limb for access to an artery. This technique generally is regarded as being most accurate in dogs. When oscillometric BP measurements are performed in dogs, the patient should be in lateral recumbency. This places the cuff at approximately the same level as the heart. In cats the patient generally remains in sternal recumbency (and minimally restrained). Most patients experience a brief acclimation period to the cuff placement. For this reason, at least three to five separate readings are obtained at 1- to 2-minute intervals. This technique can be used on awake or anesthetized patients (Figure 4-8).



The Doppler-ultrasonic flow detection system is most accurate in cats for measuring systolic BP. Again, the ventral tail base or a dorsal pedal artery (hindlimb) or the superficial palmar arterial arch (forelimb) can be used. Apply and inflate an occluding cuff. The readings are obtained by a transducer as the pressure on the cuff is reduced. Caution is recommended in interpreting results from dogs that are reported as hypertensive but have no overt clinical disease. The higher reported occurrence of falsely elevated BP in normotensive dogs measured by this method justifies additional scrutiny when interpreting Doppler BP results in dogs.


Clinically, the most common use of indirect BP measurement is in assessing cats for the presence (or absence) of systemic hypertension caused by renal insufficiency or hyperthyroidism (thyrotoxicosis). A common finding among untreated hypertensive cats is retinal detachment and blindness. Early detection and therapeutic intervention (e.g., enalapril and or amlodipine) is critical. In dogs, BP measurement is indicated in patients with chronic renal insufficiency and/or protein-losing nephropathy, hyperadrenocorticism, and diabetes mellitus. In veterinary medicine, interpretation of BP centers on the systolic BP reading, not the diastolic reading (Table 4-2).




Additional Reading


Stepien RL: Blood pressure assessment. In Ettinger SJ, Feldman EC, editors: Textbook of veterinary internal medicine, ed 6, St Louis, 2005, Elsevier.


Stepien RL: Diagnostic blood pressure measurement. In Ettinger SJ, Feldman EC, editors: Textbook of veterinary internal medicine, ed 6, St Louis, 2005, Elsevier.



Diagnostic sample collection techniques



Bacterial Culture


In previous editions of this book, methods of preparing and using selective culture media as well as identifying specific isolates was described. However, technologic advances in microbiology have largely replaced older methods of identifying bacterial isolates in practice. Furthermore, the diverse array of bacterial pathogens, requirements for unique culture media, the risk of sample contamination, and the need for subjective interpretation of results dictate that even routine bacterial cultures and identification are best reserved for the commercial laboratory equipped to carry out these increasingly complex procedures and experienced in doing so.


What follows are fundamental methods and techniques used to properly collect diagnostic specimens and the appropriate methods for transporting samples to a laboratory in order for the best possible diagnostic result to be obtained.



Direct Microscopic Examination


Before actually collecting and submitting a sample to a laboratory for bacterial culture, it is appropriate (whenever feasible to do so) to prepare, stain, and examine, under direct microscopy, exudates or fluid from the suspect material or tissue. Staining the air-dried sample with a rapid Romanowsky-type stain (e.g., Diff-Quik stain) or a Gram stain may reveal evidence of neutrophilic inflammation (neutrophilia, especially with a left shift) and occasionally degenerative neutrophils with intracellular bacteria visible. These findings greatly facilitate patient management by documenting the immediate need for interventive empiric antimicrobial therapy until definitive culture and antimicrobial susceptibility results are obtained. The absence of cytologic evidence of bacterial infection does not rule out the possibility that the patient is infected or bacteremic (Table 4-3).


Table 4-3 Common Bacterial Culture Results










































Site Commensals Pathogens
External ear canal  
Dog Malassezia, Clostridium,
Staphylococcus (a few),
Bacillus (a few); never
Streptococcus,
Pseudomonas, or Proteus
Many Staphylococcus and Malassezia
together; Pseudomonas, Proteus,
Streptococcus, Escherichia coli
Cat Not documented Staphylococcus aureus, β-hemolytic
streptococci, Pasteurella,
Pseudomonas, Proteus, E. coli,
Malassezia
Skin    
Dog Micrococcus, Clostridium,
diphtheroids, Staphylococcus
epidermidis, Corynebacterium,
Malassezia
S. aureus (coagulase positive), Proteus,
Pseudomonas, E. coli
Cat Micrococcus, Streptococcus,
S. aureus, S. epidermidis
S. aureus, Pasteurella multocida,
Bacteroides, Fusobacterium,
hemolytic streptococci
Conjunctiva Staphylococcus, Streptococcus,
Bacillus, Corynebacterium,
diphtheroids, Neisseria,
Pseudomonas
S. aureus, Bacillus, Pseudomonas, E
. coli, Aspergillus
Vagina Staphylococcus, Streptococcus,
Enterococcus, Corynebacterium,
E. coli, Haemophilus,
Pseudomonas, Peptostreptococcus, Bacteroides
Brucella canis; pure culture of organism
(especially E. coli, Staphylococcus,
Pseudomonas) when accompanied by
tissue reaction at vaginal cytology
Urine <1000* organisms per milliliter; presence of several organisms suggests contamination More than 100,000* organisms per milliliter and often pure culture; E. coli,
enterobacteria, Klebsiella, Proteus,
Pseudomonas aeruginosa, P. multocida, Staphylococcus,
Streptococcus

* Absolute numbers of bacteria depend on the collection technique.



Test Considerations


Collecting diagnostic samples for bacterial culture should be attempted as early in the disease process as possible. It is also critical to accomplish the sample collection under aseptic conditions. It is appropriate, therefore, to perform a surgical scrub of the skin or tissue from which the sample is to be collected in advance. This is especially true for tissue biopsies and fluid samples collected by needle aspiration through intact skin. Failing to adequately prepare the collection site can result in significant contamination and complicate diagnostic interpretation of results.


In addition, it is recommended to collect the diagnostic sample before the administration of antibiotics in order to minimize the risk of false-negative culture results. In the event antimicrobials have been administered to a patient with a suspected infection, and that is not responding to treatment, discontinuing treatment for 48 hours before attempting sample collection is generally recommended.


Collection of an adequate amount, or volume (fluid), is equally important in obtaining meaningful result. For example, a single sterile cotton-tipped swab of contaminated tissue should be considered inadequate sampling and inappropriate for any patient. Multiple specimens are always recommended when feasible. Also, biopsy material, surgically removed tissue, and several milliliters of fluid (e.g., urine) should be collected and placed in a sterile container that can be appropriately sealed (leak-proof container) before transport. A “clean catch” of urine in a “clean cup” is not appropriate.


Inexpensive commercial containers specifically designed for the transport of infectious material are readily available today and should be used. Many containers designed to hold bacterial samples contain buffered, nonnutritive transport media to sustain the growth of pathogenic bacteria yet minimize overgrowth of bacterial contaminants during the time required to transport the sample. Most commercial laboratories provide appropriate containment devices for the transport of bacterial samples.

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Sep 17, 2016 | Posted by in SUGERY, ORTHOPEDICS & ANESTHESIA | Comments Off on 4: Diagnostic and Therapeutic Procedures

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