Saturday, April 9, 2011

LOCAL ANALGESIA

I-LOCAL ANALGESIA
Many surgical procedures can be satisfactorily performed under the effect of local analgesia alone, and the use of sedation with this technique depends up on the species, temperament, and health of the animal, and magnitude of the operation. Sedation should be avoided in surgical procedures when the animal should not lie down, otherwise sedation should be adopted when reduction of fear and liability of sudden movement is required for achievement of efficient surgery. Moreover, the dose of sedative drug must be reduced on using certain types of local analgesics like lignocaine as it has systemic sedative effect following its absorption.   
Advantages: -
1-It is suitable for performing surgery on standing animals, accordingly injuries associating casting and prolonged recumbency can be avoided
2-The technique is simple and requires no expensive or complicated equipments
3-The technique can be performed by the surgeon himself with no need for anesthetist
Disadvantages: -
1-Injection shouldn't be performed in infected area to avoid spreading of infection
2-Direct injection of the drug at seat of incision causes delay of healing as a result of histotoxic effect of the drug
3-The amount of used local analgesic drug is relatively higher than other methods like perineural analgesia, accordingly the cost increases
LOCAL ANALGESICS: -
Desirable characteristics of local analgesic agents: -
1-It should has good penetrating qualities through body tissues                       
2-It should has rapid onset
3-It should be potent so that low concentrations can be used    
4-It should has long duration of action
5-It should has low systemic toxicity                   
6-It shouldn't be irritant to nerve and other body tissues
7-It should has reversible action      
8-It should be available in sterile solution or it can be easily sterilized
Potentiation by vasoconstriction: -
Addition of vasoconstrictor (epinephrine) to local analgesic, at concentration of 1:200,000 allows prolonged analgesic effect by vasoconstriction and delaying absorption of the drug. The maximum safe concentration of epinephrine is 1:50,000 but greater concentrations may cause local tissue ischemia and necrosis, accordingly these agents shouldn't be used in extremities, tail, or teat, etc...to avoid the possibility of ischemia and subsequent necrosis and gangrene. The exception to this rule is the epidural analgesia where concentration up to 1:10,000 may be safely used. Generally the used of analgesic agents that contain vasoconstrictor is contra-indicated in injured tissue as this tissue might be already ischemic and the further injection with epinephrine may deteriorate the condition of the ischemic tissue and causes gangrene.
Potentiation by hyaluronidase: -
Hyaluronidase is a mucolytic enzyme that hydrolyses hyaluronic acid that is known as the ground substance preventing diffusion of drug in the tissues. Incorporation of that chemical substance in the analgesic solution facilitates diffusion and penetration of the analgesic drug into the tissue and accordingly the drug will acquire faster on set.  
Advantages: -
1-It promotes diffusion and absorption of the local analgesic with which it is mixed
2-It is of particular value in nerve block, especially if the analgesic didn't deposited accurately around the nerve
Disadvantages: -
1-Toxicity although the ratio of toxic to therapeutic dose is 200:1
2-Reduction of analgesia duration
3-Increased toxicity by analgesic drug itself as a result of rapid absorption
Generally, the last two disadvantages can be counteracted by addition of epinephrine to the solution
AVAILABLE LOCAL ANALGESICS: -
A-Minor local Analgesics: -
1-Ethyl Chloride:
-It is a topical local analgesic, marketed under pressure in containers with a fine capillary nozzle and a control valve that allows the liquid to be sprayed.
-It has a very superficial and transient analgesic action, and when it is sprayed on the skin, it evaporates leading to freezing of the skin with induction of surface analgesia for 30-60 seconds.
-Its use is limited to simple incisions or punctures such as incision of abscess or hematoma.
2-Ethyl alcohol: -
-Injection of absolute alcohol around a nerve produces neuritis, degeneration, and sclerosis, however, 30% alcohol temporarily destroys sensory nerves that regenerate again after a variable period, and nerve function will return by then. Duration of block depends on;
1-The size of the nerve                    
2-Degree of destruction
-Small-unsheathed nerves may be permanently destroyed, whereas, large heavily sheathed nerves are only temporarily affected.
B-Major local Analgesics: -
Cocaine was the first available local analgesic, but its toxic effect and addictive properties in human restricted its use and availability. Nodaway, many new generations of local analgesics are available, and they vary according to their potency, toxicity and cost. The present three categories are classified according to duration of analgesic action
Analgesia duration
Drug
Duration
1Short Procaine30-60 minutes
2Intermediate Lidocaine and mepivacaine90-180 minutes
3Long Tetracaine and bupivacaine180-300 minutes
1-Short duration analgesic: -
Procaine HCl: -
Procaine HCl is a white, crystalline, water-soluble powder
Advantages: -
1-Its subcutaneous injection has an efficiency approximating that of cocaine, but it has lower toxicity especially when adrenaline HCl is added (10 times less toxic)
2-It is non-irritant
3-Relatively stable solution
4-It can be sterilized repeatedly by boiling without loss of potency
5-It is rapidly and completely detoxicated by the liver when absorbed slowly from injection site (ensured by adding adrenaline), so that a second infiltration can be carried out in the course of an hour
Disadvantages: -
1-Toxic when accidentally injected intravenous
2-It has low power of penetration
3-It can not be used for topical application or intra-synovial analgesia as it has very low power of penetration of mucous membrane
4-Decomposed by alkali
Concentration, on set, and duration: -
Use
Concentration
On set
Duration
General skin or gum infiltration  in pets2 %5 minutes
1 hour
Epidural injection1-2.5 %10 minutes
Skin or perineural use in horses and cattle 4-5 %10 minutes
2-Intermediate duration analgesic: -
A-Lignocaine or Lidocaine HCl (Xylocaine® or Debocaine®): -
Advantages: -
1-It is extremely stable solution and can be boiled with acid or alkali         
2-It can be sterilized several times even by autoclaving
3-Its onset is twice faster than procaine
4-It has longer duration of action than procaine (90 min alone and 120 min with epinephrine)
5-It has a sedative effect and the dose of tranquilizer must be reduced
6-It has higher penetration power than procaine and so it is preferred in perineural injection and it is unnecessary to add hyaluronidase to it neither for infiltration nor for nerve blocking purposes
7-It can be used for surface analgesia by intra-synovial injection, for the cornea, or for mucous membranes (4%), particularly those of the throat and larynx, prior to endotracheal intubation
Disadvantages: -
Toxicity by over dose that is expressed by drowsiness, twitching and respiratory depression, and finally convulsions and hypotension ensue. Accordingly the toxic dose is known to be
Animal
Dose in gm
Dose in ml (2%)
Horse and cattle6300 ml 2 %
Dog0.630 ml 2 %
Concentration: -
1-General infiltration (0.5:1 % with no vasoconstrictor)
2-Epidural and nerve block (2% with or without vasoconstrictor)
B-Mepivacaine HCl (Mepacaine®): -
This compound closely resembles lignocaine HCl, and widely used for human dentistry
Advantages: -
1-It is slightly less toxic, even slow intravenous injection over 20 minutes in dog by a dose of 29 mg\ kg, produces convulsion that is followed by sedation
2-It has no vasodilatory effect, making the addition of a vasoconstrictor unnecessary. However, a commercial product with levonordefrin is available in market (Mepacaine-L®).
Concentration: -
For infiltration and nerve block (1-2%) is satisfactory, but generally it is available as ampoules of 1.8 ml of 2 % Mepivacaine HCl with or without levonordefrin.
3-Long duration analgesic: -
A-Tetracaine HCl (Pontocaine®): -
Advantages: -
1-The onset of analgesia is 5-10 minutes                           
2-It is 12 times potent than procaine
3-Its toxicity 10 times that of procaine
4-Lesser interference with corneal healing than other agents, so it is the drug of choice for corneal analgesia
Disadvantages: -
It can't be autoclaved.
Concentration: -
*For the eye (0.2% for 120 min)
*For infiltration and nerve block (0.1%)
B-Bupivacaine HCl (Marcaine®): -
Advantages: -
1-Stable solution on boiling with acid and alkali and shows no change on repeated autoclaving.
2-Represented in different concentrations with or without adrenaline
3-More potent 8 times than procaine and 4 times than lidocaine HCl so it is used as 0.5 % solution         
4-It has greater margin of safety than lignocaine
5-Onset is similar to lignocaine but its effect lasting for 4-6 hours (twice longer period of analgesia), so it is indicated for use in situation where prolonged analgesia is required like relief of pain in equine during acute laminitis
Concentration: -
Aim of use
Concentration
Infiltration 0.25%
Nerve block0.5%
Epidural analgesia0.75%
TYPES OF LOCAL ANALGESIA: -
I-SURFACE ANALGESIA: -
A-Topical analgesia: -
1-Surface analgesia can be produced by freezing of superficial layers of skin by ethyl chloride, ether, or carbonic acid snow, as a result of their rapid volatilization. Their action is superficial and transient, and their use is limited to simple surgical interferences like incision of an abscess. Excessive use may lead to necrosis, and the thawing after their use is very painful.
2-Surface analgesia can be performed by using lignocaine ointment that is applied by skin friction for relief of pruritis
3-Surface analgesia may be performed by using lignocaine 2% aqueous solution topically for relief of superficial abraded or eczematous area
4-Surface analgesia of mucous membrane of the glans penis and vulva can be produced by topical use of lignocaine 2% aqueous solution
5-Surface analgesia of urethral mucous membrane can be adopted by lignocaine 2% gel that works as lubricant and analgesic
6-Surface analgesia of the nasal mucous membrane can be performed by lignocaine 4% spray for trans-nasal passage of stomach tube in dog or for surgical procedures of the nasal chamber in the horse
7-Surface analgesia of the cornea can be performed by topical instillation of 4% lignocaine or 0.2% Tetracaine®
8-Surface analgesia of the joints can be performed by intra-synovial injection of 2 % lignocaine
B-Intrasynovial: -
Surface analgesia is employed for relief of pain arises from pathological conditions of the joint and tendon sheath. The technique involves direct injection of local analgesic into the joint or tendon sheath with mechanical manipulation of the joint or sheath for spreading of the drug, and when the joint or tendon sheath is distended with synovia, it is recommended to aspirate some the fluid to prevent dilution of analgesic. Analgesia usually arises 5-10 minutes after injection and lasts up to 1 hour, as a result of direct effect of the drug on the surface of the joint or sheath.
Uses: -
1-Therapeutic, like relief of pain during arthritis
2-Diagnostic, for diagnosis of arthritis or lameness (therapeutic diagnosis)
II-INFILTRATION ANALGESIA: -
This technique can be used for minor operations or even for major operation either alone or in adjunction with sedation or basal narcosis.
A-Intra-dermal: -
It is a process through which analgesic drug is injected intra-dermal to facilitate injection in animals. The main point of this technique is the humanity as it reduces pain during subsequent procedure of infiltration analgesia.
B-Linear infiltration: -
This method can be performed by creation of insensitive intra-dermal weal through which the needle is inserted subcutaneously into two opposite directions to create analgesic line, and by this method a line of analgesia that has double length of the needle can be created with minimal skin bricking. Usually the drug is injected while the needle is dragged out of the subcutaneous tissue and the amount of required analgesic is 1 ml\ cm2. Although sensation is mainly confined to the skin, but in some circumstances it is recommended to infiltrate the muscular layer beneath the skin as sensory nerves pass through it and this will achieve better analgesia, moreover, involvement of motor nerves that passes through the muscles reduces movement of the muscles during incision. A clear example of this is the linear infiltration of the left flank in cattle that involves both subcutaneous tissue and underlying muscles for induction of rumenotomy or cesarean section. A simultaneous technique is the creation of insensitive weals beside each other in the form of line.
Advantages: -
1-Simple and easy technique
2-It consumes smaller amount of anesthetic and shorter time than inverted-L technique
Disadvantages: -1-Dealyed healing
2-Changes in the anatomical features
3-Consumption of large amount of drug than paravetribral technique
C-Field block analgesia: -
1-Cup shape field block: -
It is an inverted pyramidal shape analgesic area that is created by two punctures, and can be used when the pass of nerve supply is not exactly known. Usually it is applied to an area of bulky musculature.
Advantages: -
1-Absence of anatomical distortion at seat of incision
2-When the drug contains vasoconstrictor, it will produce efficient ischemia
3-Complete muscular relaxation
4-No retardation of healing
2-Inverted-L block: -
It is a field block technique through which only the dorsal and anterior aspects of the flank region are injected subcutaneously with local analgesic solution to produce complete analgesia of the flank for induction of rumenotomy or cesarean. The main point of neglecting the posterior aspect is that the nerves pass to the flank from the dorsal and anterior aspects while is passes caudo-ventrally.
Advantages: -
1-Seat of injection is far from incision line (not interfere with healing)
2-Simple technique and requires no technical skills or complicated equipments
3-It does not cause change of the anatomical features at seat of incision
Disadvantages: -
1-It consumes larger amount of anesthetic than linear infiltration and paravetribral
2-It consumes longer time than linear infiltration
3-Ring block: -
It is a technique used for induction of analgesia by injection of analgesic drug in a ring manner at one level like in teat or digit. On induction of analgesia of the teat, adrenaline shouldn't be incorporated in the injected solution as vasoconstriction may cause necrosis of the compromised teat. The technique is useful for surgical repair of presternal bursitis in buffalo calves, umbilical hernia, amputation of digit etc...
III-INTRAVENOUS REGIONAL ANALGESIA: -
It is a simple technique usually used in dogs and can be performed by injection of 2-3 ml of 1% lignocaine intravenous in the cephalic vein after application of tourniquet on the forearm. Analgesia allover the limb can be achieved and the effect can be reversed just the tourniquet is removed.
IV-LOCAL ANALGESIA OF FRACTURE: -
It is a simple technique performed by injection of 2-5 ml of 1% lignocaine (small animals) or 10-15 ml of 1% lignocaine (large animals) into the hematoma as near as possible to the ends of bone. Analgesia will ensue within 5 minutes after injection.


References: Hall, C.W. and Clarke, K.W. (1983), Veterinary anesthesia, 8th edition; Hall, L.W. (1978), Wrights veterinaray anesthesia and analgesia, 7th edition

ASEPTIC TECHNIQUE GUIDE

ASEPTIC TECHNIQUE GUIDE




Terminology: -



Sepsis: Presence of living pathogenic microorganism within the tissue



Sterile: Presence of no microorganism



Sanitize: Reduction of the number of microorganisms to a safe level



Antiseptics:



They are drugs, substances, or chemicals that applied topically to the living tissue to kill microorganisms



Disinfectants:



They are drugs, substances, or chemicals that applied to inamonate objects or non-living surfaces to kill microorganisms



Characters of ideal antiseptic or disinfectant: -



1-It is safe, not absorbed by the skin of the animal, and neither harmful (has adverse effect) to living tissue nor corrosive for non living surfaces



2-Highly effective against all microorganism at low concentration



3-Effective in presence of organic matter 5-Incompatable with other drugs



4-Soluble in water, stable, penetrate tissue surface 6-Fast acting with long duration



7-Non staining and odorless



Mechanism of action of antiseptics and disinfectants: -



1-Coagulation of bacterial cell protein



2-Ulteration of cell wall permeability leading to loss of essential substances or entry of unneeded substances



3-Interference with enzymatic system



Classification of disinfections: -



I-PHYSICAL: -



Physical sterilization by dry or moist heat is the most commonly used method of sterilization. 1-Dry heat (baking, flaming): -



A-Direct flaming: -



Advantages:



Simple and cheap method



Disadvantages:



Dullness of sharp instruments



B-Hot air (Oven): -



It is an effective method of sterilizing metal instruments and glassware (1-2 hours at a temperature over 200°C)



Advantages:



Excellent method of sterilization



Disadvantages:



1-High cost



2-It is not suitable method of sterilization of plastic or rubbery materials



2-Moist heat: -



It is commonly used method of sterilizing instruments, clothes, suture materials, and any other utensils



A-Boiling: -



Boiling by using distilled water in which has been added sodium carbonate 2 % at 100°C for at least 20 minutes can be used for sterilization of suture material, syringes and needles



Advantages:



Simple and cheap method



Disadvantages:



It is not recommended for aseptic surgery since;



1-It is not effective in killing bacterial spores



2-It tends to dull sharp instruments



B-Steam under pressure sterilization (autoclaving): -



It can be done at 120°C and 1.5 lb/ square inch atmosphere pressure for 1 to 2 hours. Advantages:



1-It is a good penetrating, bacteriocidal and economical method



Disadvantages:



1-It dulls sharp instruments 2-It scorchs fabrics



3-It may leave packs wet 4-It will not sterilize grease or oil materials



II-CHEMICAL: -



1-Oxidizing agents: -



These substances liberate nascent oxygen and so it is affected by the presence of organic matters



A-Halogens (Chlorine)



B-Peroxides (H2O2)



C-Potassium permanganate

2-Reducing agents: -



-An example of reducing agent is formaline, which is formaldehyde 40% in water.



-It is not affected by organic matter and has the ability to form toxoid with bacterial toxins



-It can be used as urinary antiseptic in acidic urine, as it is released from hexamine



-It can be used in the form of gas when mixed with Potassium permanganates.



3-Heavy metal: -



A-Mercury salts



i-Mercuric chloride used as skin antiseptic



ii-Mercuric nitrate and oxide used as eye ointment



iii-Bin iodide of mercury % in lanoline used as blister or counter irritant



iv-Organic mercury compounds act as disinfectants by liberating mercury ions as thiomersolates for wounds, skin, and instruments



B-Silver salts



Silver nitrate is an astringent that can be used for corneal ulcers



C-Copper salts



Copper sulfate % can be used as astringent fungicidal and germicidal



D-Zinc salts



Like zinc sulfate, zinc oxide, and zinc chloride



E-Arsenical salts



Arsanilic acid can be used orally as intestinal antiseptic



4-Acid and alkalis: -



Caustic soda and quick lime can be used for disinfection of buildings but they are corrosive



5-Alcohols: -



Ethyl alcohol 70% can be used for skin disinfection



6-Phenol and its derivatives



A-Phenol



It can be used as 2% solution for disinfection, or it can be used as it is for corneal ulcers



B-Crysol



Used as 0.5- % as intestinal antiseptic



C-Lysol



It can be used for disinfection of non-living objects



D-Chloroxylenol (Dittol®)



It is none irritant antiseptic for intact skin in concentration of 2%



E-Picric acid



It is used as antiseptic for burns



7-Alcohol formaline mixture at equal volumes or organic dyes such as acriflavin: -



They are used for sterilization of optical instruments and catheters



8-Gas sterilization with Ethylene Oxide gas (EO): -



Advantages:



1-It is both bactericidal and sporicidal



2-Their penetration and effectiveness at relatively low temperatures make them useful for sterilizing surgical supplies made of leather, wool, paper, plastics and other materials that would be damaged by the heat



3-It sterilizes electrical and optical equipment effectively and do not dull instruments



Disadvantages:



Materials that have been sterilized with Ethylene Oxide must be aerated for 1 to 7 days, depending on the material, otherwise residual gas may diffuse from the goods and irritates living tissues.



To perform aseptic surgery technique, strict measures should be taken to prevent contamination of the surgical wound, and to achieve this, the operating room, the surgery packs, the patient, and the surgeon must follow rigid routine procedures to insure such aseptic surgery technique



1-Operating or surgery room: -



Construction of operating room:



1-It is preferred to be isolated 2-It must be subjected to rigid policies



3-It should be with one exit in order to restrict unnecessary movement of personnel as well as to minimize the opening and closing of doors during surgery



4-The operating room should be in direct connection with the surgery preparation room and the surgical scrub area (used for preparation of surgical patients and as a post surgical recovery room)



5-The operating room should be supplied with good lighting facilities, casting beds and cushions operating tables and instrument carts and trolleys. Permanently installed hydraulic operating table is likely to be encountered in large animal surgery room. When circumstances entail that surgery must be carried out in an open yard, the clinician must select the site most suitable for the procedure.



6-If a minor surgical procedure is to be carried out on the standing position, measures should be taken, to secure the animal either in stanchion or in a box stall. When recumbency is mandatory, consideration must be given to the area or location in which the surgery will be performed preferably in a grass field or paddock in which a casting bed is required. The major drawbacks to this are the saturation of air with dust as well as the insect problems.



Surgery room cleanliness:



1-Cleaning of the surgery room should be done by well-trained housekeeping personnel



2-Daily cleaning consists of damp dusting of all flat surfaces, lights and furniture approximately one hour before surgery



3-Weekly cleansing routines must be established and it consists of whipping down of walls and ceilings with a germicidal cleaning solution. Cabinets and other operating room equipment should be cleansed. Operating tables should be cleansed after each operation with germicidal solution.



4-Buckets should be carefully cleansed and disinfected.



5-After surgery, areas contaminated by organic debris like blood should be cleaned with detergent and disinfectant



2-Surgery Packs: -



All materials and equipment used in a surgical procedure or entering the operative field must be sterilized.



1-Instruments and materials must be clean prior to sterilization



2-Post-operative cleaning to remove blood can be facilitated by soaking all materials and instruments in cold water and detergent



3-Gowns, drapes and other fabrics must be laundered



4-After drying the equipment and supplies they are arranged for pack preparation



5-The instruments and materials included in a pack vary with the surgical procedure or with the surgeon preference. All materials are packed either in sterilizing drums or wrapped with clean towel and double thick paper without contamination. Autoclaving is the most widely used method of surgical pack sterilization. Properly wrapped sterilized packs will remain sterile for up to 6 months if properly stored. Packs stored in sealed plastic bags remain sterile for up to one year.



3-Preparation of the operative site: -



Preparation of the operative site includes the following;



1-Clipping of hair which is best achieved by the use of an electric clipper. Shaving the hair coat is not always preferable since it takes long time for shaving an area and it produces erythema of the shaved skin.



2-Cleansing with a surgical scrub agents such as povidon iodine (Betadine®) or hexachlorophene and warm water to remove dirt and water insoluble materials. Scrubbing with a sponge should be in a circular manner starting at the incision site and moving outwards to the periphery then the sponge is discarded. Scrubbing of the operated area should be twice.



3-A germicidal solution such as alcohol 70 % is applied.



4-A skin antiseptic solution, preferably 2.5 % tincture iodine is applied.



Draping the patient:



The basic set of drapes pack consists of 4 pieces each approximately 120x90 cm and one main drape 200x205 cm with a rectangular window. The caudal drape is applied first, leaving a double thickness adjacent to the prepared area. The cranial drape is applied in a similar manner. The side drapes are then placed, leaving a suitable area exposed for the incision. The drapes are held in position with towel forceps. The patient and the entire operating table are then covered with the main drape that has a window. The window should enclose the area of the incision. The head of the patient is left uncovered for purposes of observation during surgery.



4-Preparation of the surgeon and assistants: -



1-Members of the surgical team and operating room personnel should be appropriately clothed.



2-Observation gowns and disposable shoe covers can be worn over the usual clothes of operating room personnel and others entering the operating room.



3-Caps and masks are also necessary.



4-Cloth flaps, masks and gowns must be laundered after each use



Preparation of the hands:



1-Before preparation of the hands for sterile surgery, the fingernails are cut short.



2-The cap and mask should be worn before scrubbing commences.



3-A deep sink with facilities that permit the adjustment of water flow without touching the faucet is very useful (a knee or foot control is preferred). Warm water should be used for scrubbing. The surgical scrubbing agents of preference are povidone-iodine and hexachlorophene. The hands and forearms are washed for 30 to 60 seconds with the surgical scrub. The hands are then scrubbed with a sterile brush with stiff bristles, scrubbing agent and water. Each surface of each finger should be scrubbed as well as the surface of the hands and arms with special attention to the nails and between the fingers. The process is repeated on the opposite arm. Scrubbing should be not less than 5 minutes. Both arms are then rinsed with the hands still held above the elbows. The application of alcohol 70 % to the hands and forearms following scrubbing is preferred, then drying of the hands and arms by means of sterile towel.



Gowning and Gloving:



The sterile gown and towel wrap or drums are opened by an assistant. The gown is lifted from the sterile wrap and held away from the table. The surgeon unfolds the gown by placing his hands in the appropriate armholes. The arms are pushed in the sleeves to the cuff. An assistant closes the neck and ties the inside waist tie. The gloves are worn and folded over the cuffs of the sleeves. Some operations need rigid aseptic precautions so that two pairs of gloves should be worn.



The instruments:



Instrument trays are presented, with the assistant carefully removing the paper wrap or cover. The surgeon places the instruments on the sterile wrapped instrument stand.

...ANESTHESIA ...

...ANESTHESIA ...




Satisfactory anesthesia is very important for both humanitarian and technical efficacy. Humanity ensures gentle handling of the animal with minimal restraint to minimize possible injury to the animal, while technical efficacy ensures protection of personnel from bite, scratch, kick, inhalation of volatile anesthetics in the animal breath, or accidental self injection by sedative or addictive drugs.



The veterinary anesthetist deals with variety of animal species that exhibit variation in size, temperament, and anatomical and physiological development. Response to anesthesia not only varies according to species and breed, but it also varies among individuals of the same breed. Fear and aggressive reaction of animals to casting (prior to anesthesia) and struggling to escape breathing irritant gases, increase the difficulty of anesthetic administration and brain activity that in turn affects the amount of required anesthetic. Accordingly, sedatives and tranquilizers are used pre-anesthetic to reduce brain activity, fear and struggling to reduce anesthetic dose and to help smooth induction and recovery of anesthesia.



Terminology: -



1-Anesthesia: -



It is the art and the science related to production of insensibility



2-General anesthesia: -



It is a state of unconsciousness as a result of controlled reversible intoxication of the central nervous system, and characterized by lowered sensitivity to external stimuli with diminished motor response to such stimuli.



3-Anesthetic agent: -



It is the substance that produces controllable loss of consciousness and absence of motor response to noxious stimuli.



4-Analgesic agent: -



It is the substance that temporarily abolishes awareness of pain



5-Local analgesic: -



It is a substance that when applied to the nerve endings or nerve fibers, temporarily prevents the conduction of impulses by the nerve, by interference with transmission of impulses concerned with appreciation of pain.



6-Local analgesia: -



It is the loss of sensation in a limited area of the body



7-Regional analgesia: -



It is insensibility in a large area of the body, or it is a process through which certain region retained insensible



8-Narcotic agent: -



It is the substance that produces insensibility, or stupor bordering upon it, and simple stimuli like noise can only produce temporary partial arousal. Accordingly all anesthetic agents are narcotic but many narcotics are not anesthetics.



9-Hypnotic agent: -



It is a narcotic agent that produces sleeping, which is a state of physiological unconsciousness, from which the animal can easily be awakened by wide variety of stimuli.



10-Sedative: -



It is a narcotic agent that can be used to calm a nervous, excited, or vicious animal, and these drugs cause drowsiness.



11-Ataractic or tranquilizer: -



It is substance that produces sedation without drowsiness.



AIMS OF ANESTHESIA: -



1-Humanity point of view like prevention of pain during surgical interference



2-Creation of a safe state under which the surgeon and assistants can work



EXAMINATION OF THE ANIMAL: -



The general condition of the animal should be evaluated and recorded prior to anesthesia and surgery, including history, temperature, pulse rate, and respiration rate etc....



PREPARATION OF ANIMAL FOR ANESTHESIA: -



1-Fastening 24 hours prior to operation



2-Fluid therapy according to animal state



3-Preanesthetic medication according to the nature of anesthesia, surgery, and animal species



TYPES OF ANESTHESIA: -



I-Substances have selective transient paralytic action on sensory nerves



I-1-Local analgesia



I-1-A-Surface application



I-1-A-i-Topical application



I-1-A-ii-Intra-synovial analgesia



I-1-B- Intra-dermal and Subcutaneous infiltration analgesia



I-1-B-i-Intra or sub-dermal infiltration



I-1-B-ii-Linear infiltration analgesia



I-1-B-iii-Field block analgesia



I-1-B-iii-1-Cup shape



I-1-B-iii-2-Inverted-L block



I-1-B-iii-3-Ring block



2-Regional analgesia



2-A-Perineural nerve block



2-A-i-Peripheral nerve block



2-A-ii-Paravertebral nerve block



2-B-Spinal nerve block



2-B-i-Epidural analgesia



2-B-i-1-Caudal epidural



2-B-i-2-Segmental lumbar epidural



2-B-ii-Intrathecal analgesia or sub arachnoid



II-Sedation, narcosis, and pre-anesthetic medication



II-1-In combination with local or regional analgesia



II-2-In adjunction to general anesthesia



III-Substances have depressant paralytic action on the cns producing progressive loss of consciousness and voluntary motor function (general anesthesia)



III-1-By inhalation (volatile anesthesia)



III-2-By intravenous injection



III-3-By combination of the mentioned types with or without premeditation



GENERAL CONSIDERATIONS IN SELECTING ANESTHETIC METHOD:



1-Nature and magnitude of the operation: -



Local infiltration is sufficient for simple interferences like incision of superficial abscess or neoplasm, or castration in immature animals. However some simple surgical operations can't be performed by local infiltration as a result of severe fibrosis, temperament of the animal, or severity and intensity of surgical procedure.



2-Site of operation: -



Presence of some critical structures in vicinity of site of operation may render local infiltration insufficient as the movement of the animal may endanger his life, and the example is the surgery for retropharyngeal abscess.



3-Duration of operation: -



The duration of operation affects the choice of anesthetic method, especially when adopting general anesthesia. Short-duration, simple dental operations, can be performed by using ultra-short acting barbiturates, while longer interferences can be performed by using longer-acting barbiturates with local analgesia, or inhalation anesthesia.



Pre-anesthetic medication should be considered when the operation is a major operation with long duration and it is required that the animal remain quite for several hours after surgery. Pre-anesthetic medications not only reduce the amount of anesthetic agent and increase duration of anesthesia, but also control undesirable effect of some anesthetics like salivation.



4-Species and breed of animal: -



Not only size and temperament of the animal affect the choice of anesthetic method, but also the anatomy and physiology of some species affect that choice. Generally the larger size animals have greater difficulties and dangers in induction and maintenance of general anesthesia. The safe satisfactory methods for general anesthesia in pets may be unsuitable for large animals, especially for heavy vigorous one, as the upset of locomotor coordination and prolonged recumbency may entail risks.



Not all species react to drugs in the same manner, as horse may be excited when administered sub-anesthetic dose of barbiturate, and cat may become maniac when given large dose of morphine.



Increased susceptibility for toxicity by anesthesia affected by two main factors, the prolonged fasting (predisposes to depletion of liver glycogen and reduced detoxication capacity of non-volatile anesthetic agents), and disease condition (toxemia predisposes to degeneration of parenchymatous organs as liver leading to reduction of its detoxication capacity, also toxemic animal seems to need smaller dose).



A-The Horse: -



The animal should be adequately restrained to ensure safety of the veterinarian and the animal himself. Casting methods of conscious animal frightening and expose him to injury, accordingly, many muscle paralyzing drugs can be sued to induce casting without endangering the animal.



The possibility of blocking of many peripheral nerves should be considered, and on using anesthetic method that is associated with slow recovery, veterinarians have to ensure that this recovery period will be free from excitement.



Some sedatives and non-volatile anesthetics are precluded from use in horse, as they don't have some requirements like; the ability of the animal to rise to his feet soon after surgery; and at the outside within 1-2 hours with strong enough locomotor power and coordination to prevent the animal from falling.



B-Ruminants: -



Generally they are unsuitable candidate for inhalation anesthesia unless endotracheal tube is used, but under field condition, light general anesthesia by intravenous injection has satisfactory results. However the simpler regional analgesic techniques in this species and side effects of general anesthesia make regional anesthesia more popular in these species.



C-The Dog: -



General anesthesia has a high degree of perfection in this species that make this method so popular for veterinarians not only for surgery but also for examination procedures in the animal. Some breeds have brachicephalic skull predisposing them to asphyxia as a result of relaxation of jaw muscles during general anesthesia and accordingly endotracheal tube should be considered on inducing general anesthesia in such breeds.



D-The Cat: -



Cat is a difficult subject to be anesthetized quietly and safely as restraint provokes violent struggling. Accordingly cat should be handled quietly with minimal restraint then general anesthesia can be induced by slow intravenous barbiturate.





References: Hall, C.W. and Clarke, K.W. (1983), Veterinary anesthesia, 8th edition; Hall, L.W. (1978), Wrights veterinaray anesthesia and analgesia, 7th edition
Friday, April 8, 2011

Toxoplasmosis

Toxoplasmosis

Toxoplasmosis is contagious disease of swine, sheep and other species characterized with encephalitis, pneumonia and neonatal mortality. It is caused by protozoon Toxoplasma gondii in animals and humans. Toxoplasma is most frequently found in pigs and sheep. Young animals are infected to a lesser degree than old animals. Cattle are rarely affected with clinical toxoplasmosis. Young pigs may die from pneumonia caused by toxoplasmosis.

Humans can get infected with Toxoplasma cysts by ingestion of uncooked animal tissue. In humans clinical symptoms may vary from fever, malaise, skin rash, pneumonia, myocarditis, lymphadenopathy and encephalitis. Infected pregnant women may transfer the tachyzoites to the fetus.



Life cycleAsexual, sexual and oocyst stages of this organism develop in the small intestine of wild and domestic cats. Cats get infected by eating mice or birds or animal tissue containing infective oocysts. In the intestine, the parasite develops through the typical coccidian life cycle. Unsporulated oocysts are shed in the faeces.

After a few days the oocysts sporulate and become infective for over a year. The oocysts are further ingested by the intermediate host (pig, sheep, cattle and humans). From the intestine, oocysts move to various tissues including myocardium, lungs, placenta and most frequently to muscle, brain and liver where they encyst. In the host, they may remain viable for the life span of the host. By eating the infected tissue mice, birds, cats and humans may get infected. The life cycle is then completed.

Ante-mortem findings 1. Neonatal mortality
2. Fever (40 - 42oC) and pneumonia in young pigs
3. Difficult breathing and coughing
4. Weakness and wasting
5. Incoordination and trembling
6. Diarrhoea
7. Abortion in pregnant sows and stillbirths

Post-mortem findings 1. neumonia
2. Hydrothorax
3. Ascites
4. Intestinal ulceration
5. Necrosis in the liver, spleen and kidneys
6. Inflammation of the lymph nodes
7. Multiple granulomatous lesion in the brain

JudgmentCarcasses of animals showing clinical signs of acute disease are condemned. Recovered and reactor animals are approved.

Differential diagnosisAbortion in pigs: Brucellosis, leptospirosis, porcine parvovirus infection, hog cholera and Aujeszky's disease. Encephalitis: Salt poisoning, chlorinated hydrocarbons, lead, mercury, Vitamin A deficiency, hypoglycaemia, encephalomalacia, meningitis, rabies and scrapie

Tuesday, April 5, 2011

Collection and Submission of Laboratory Samples: Introduction

Each veterinary diagnostic laboratory offers a unique set of diagnostic tests that is subject to frequent changes as better tests become available. The protocols for sample collection and submission are also subject to change. The practitioner and diagnostic laboratory staff must maintain good communication in order to complete their diagnostic efforts efficiently and provide optimal service to the animal owner. Practitioners must be specific and clear in their test requests. The laboratory staff can provide guidance when there are questions regarding sample collection and handling, as well as offering assistance in interpretation of test results. Most diagnostic laboratories publish user guidelines with preferred protocols for sample collection and submission, but the following broad recommendations are fairly standard.Regardless of the type of submission, a detailed case history should be included with the samples to assist laboratory personnel in determining a diagnosis. The information should include: owner, species, breed, sex, age, animal identification, clinical signs, gross appearance (including size and location) of the lesion(s), previous treatment (if any), time of recurrence from any previous treatment, and morbidity/mortality in the group. If a zoonotic disease is suspected, this should also be clearly indicated on the submission sheet to alert lab personnel. The submission form should be placed in a waterproof bag to protect it from any fluids that might be present in the packaged materials. Waterproof markers should be used when labeling specimen bags and containers.  

Histology:

Microscopic examination of adequately prepared tissue sections is a valuable aid to diagnosis. Cellular changes in diseased tissues are often characteristic of a specific disease or group of diseases. Use of this relatively rapid and inexpensive diagnostic technique can often result in substantial savings in time, money, and animal life. The increasing number of immunohistochemical tests that can be applied to formalin-fixed tissue has further reinforced the utility of this diagnostic technique.Autolyzed tissues are generally useless for histopathologic examination; prompt necropsy examination and organ sampling are critical. Tissues collected for histologic examination should be representative of any lesions present and, if possible, should include some of the apparently normal surrounding tissue. Tissue should not be frozen before fixation. Samples of the various organs should be cut <1 cm thick (preferably 7 mm) and placed immediately into ≥10 times their volume of phosphate-buffered 10% formalin for fixation. Thin slices or cubes ensure adequate penetration of the fixative. Because the GI mucosa decomposes rapidly, short sections of gut must be opened lengthwise to allow adequate fixation. The tissues should remain in fixative for ≥24 hr; after this initial fixation, the samples may be placed in a smaller volume of fresh formalin for shipment. Samples should be shipped in unbreakable containers and packed in a manner that prevents spillage during shipment. Fixed tissues should be protected from freezing.If the animal exhibited CNS signs, the brain and portions of the spinal cord should be submitted. When the whole brain may be required, it should be placed in concentrated formalin (40% formaldehyde), to which water is added slowly and mixed until the brain sinks to just below the surface but not to the bottom. The brain should remain in this solution for ≥24 hr, after which it may be removed and placed in a solid container in 10% formalin and either mailed (suitably packed) or held until processing is desired. Often, the brain is halved longitudinally and one-half sent unfixed (fresh), properly refrigerated, for microbiologic tests.Biopsy samples should be fixed in the same manner as necropsy tissues. Small tumors (<1 cm) should be cut in half, and larger tumors into small pieces or several representative samples.

Microbiology:

Laboratory techniques and capabilities for microbiologic examination vary; available tests include bacteriologic culture, virus isolation, in-situ hybridization, PCR, fluorescent antibody tests, latex agglutination tests, and ELISA. Therefore, it is critical to obtain specific instructions from the diagnostic laboratory on sample collection and handling. Usually, unfixed specimens are submitted and should be collected aseptically, as soon as possible after death. If PCR testing is to be performed, it is particularly important to avoid cross-contamination between multiple animals in a submission; this applies to tissues, fluids, and even dissection instruments. Tissues for most microbiologic assays may be frozen before shipment, but freezing is undesirable if samples can be chilled and delivered directly to the laboratory in a short period. Adequate refrigerant should be provided so that samples will remain chilled until they reach the laboratory.

Toxicology:
If a known toxin is suspected, a specific analysis should always be requested—laboratories cannot just "check for poisoning." A complete description of clinical and epidemiologic findings may help differentiate poisoning from infectious diseases that can simulate poisoning. Appropriate samples for many of the more common toxicities are listed in Table:Guidelines for Submitting Samples for Toxicologic Examination.
If there is doubt about sample submission procedures, the laboratory should be contacted.Tissues or fluids for chemical analysis should be as fresh as possible and kept in a refrigerator or preserved chemically; packing with ice is preferred. A polystyrene refrigerator box, metal can, or stout cardboard box may be used for shipment. Packing must withstand breakage if the ice melts. Samples can be preserved for 72 hr if packed in a styrofoam box with dry ice. Packages containing dry ice must be so labeled on the outside and suitably vented to prevent pressure buildup. Adequate refrigeration is of special importance when submitting clean body fluids (such as those obtained from an eye) and material for nitrate or nitrite analysis; these salts are rapidly metabolized by microorganisms.The containers for packing and transporting specimens should be free of chemicals. Plastic containers, both bags and jars, are ideal; jars with metal screw caps should be avoided. Samples should be packed individually. Containers must be labeled with all information necessary to identify the sample and, if mailed, must conform to postal regulations.If legal action is a possibility, all containers for shipment should be either sealed so that tampering can be detected or hand-carried to the laboratory and a receipt obtained. The chain of custody must be accurately documented.

If feed or water is suspected as the source of poisoning, samples of these and any descriptive feed tag should accompany the tissue samples. If at all possible, a representative composite sample of the feed should be submitted from the suspect lot or shipment. In some instances, if an adequate amount of involved feed is available, some of it may be fed to experimental animals in an effort to reproduce the signs and lesions seen in the field cases.

Hematology:

Routine studies require anticoagulated whole blood and several blood smears. Blood smears should be prepared immediately after the sample has been collected to minimize cell deterioration. Anticoagulated blood should be kept refrigerated; blood smears should not. Ethylenediamine tetra-acetic acid (EDTA) is the anticoagulant of choice for a CBC because it best preserves the cellular components of the blood and prevents platelet aggregation. Blood for coagulation testing should be collected into a blue top tube, which contains sodium citrate. After mixing, the sample should be centrifuged for 5 min, and then plasma should be removed and transferred to a clean tube without anticoagulant. The plasma should be kept frozen until the time of analysis. Whole blood should not be frozen because this causes cell lysis and gross hemolysis, which interfere with testing.



Clinical Chemistry:

Most clinical chemistry tests require serum, but an occasional test may require plasma. Anticoagulants present in plasma may interfere with tests; therefore, serum should always be submitted unless plasma is specifically requested. Because lipemia can interfere with a number of chemistry tests, dogs and cats should be fasted for 12 hr before samples are collected. For serum samples, the blood should be drawn into a red top tube or a separator tube. The sample should be held at room temperature for 20-30 min to allow complete clot formation and retraction. Incomplete clot formation may cause the serum to gel due to latent fibrin formation. The clot should be separated from the glass by gently running an applicator stick around the tube walls ("rimming"). The sample should then be centrifuged at high speed (~1,000 g; 2,200 rpm) for 10 min. Rough handling of the sample or incomplete separation of erythrocytes from serum may promote hemolysis, which can interfere with certain tests. If the sample has been collected into a serum separator tube, centrifugation will cause a layer of silicon gel to lodge between the packed cells and the serum. The gel layer should be inspected to ensure the integrity of the barrier, and recentrifugation is recommended if there is a visible crack in this layer. If a red top tube has been used, the serum should be removed and transferred to a clean tube. Serum should be refrigerated or frozen until analyzed. Many commercial laboratories provide sample containers and mailers.  



Serology:


Serology generally requires serum, but plasma is often satisfactory. Samples should be collected as described for clinical chemistry tests and should always be free of hemolysis. In some instances, paired samples may be required for an adequate diagnosis. The acute sample should be collected early in the course of the disease and frozen. The convalescent sample should be collected 10-14 days later, and both samples should be forwarded to the laboratory at the same time.


Cytology:

Air-dried smears are usually acceptable. Rapid air drying of smears minimizes cell distortion, thereby enhancing diagnostic quality. However, depending on the method of staining used, some laboratories prefer alcohol-fixed smears. Samples can be obtained by fine-needle aspiration or by scraping. Imprints (touch preparations) of external lesions can also be used, although these tend to have a greater degree of contamination. Aspirated material should always be smeared before air drying. Smears of fluid can be prepared using a traditional blood smearing technique. Highly cellular fluids may be smeared directly; fluids of low cellularity should be centrifuged to concentrate the cells. Thick material or viscous fluid is more readily smeared using a squash technique in which a second glass slide is placed over the aspirated material and then slid rapidly and smoothly down the length of the lower slide. Blood or cytologic smears should never be mailed to the laboratory in the same package with formalin-fixed tissues because formalin vapors will produce artifacts in the specimen.

Fluid Analysis:


Body cavity effusions should be analyzed. Fluid analysis usually includes determination of protein content and total cell count and cytologic examination. Other tests may be performed depending on the source (eg, synovial fluid) or appearance (eg, chylous fluid) of the effusion. A sample of effusion should be collected into an EDTA (purple top) tube for routine analysis. A second sample should be collected into a serum (red top) tube if any biochemical analyses (eg, triglyceride, cholesterol, lipase) are to be performed or if a bacterial culture is desired. Smears for cytologic examination should be prepared immediately after the sample has been collected to minimize cell deterioration and other in vitro artifacts.
Sunday, April 3, 2011
Saturday, April 2, 2011

Reticuloruminal Motility

Reticuloruminal Motility





An orderly pattern of ruminal motility is initiated early in life and, except for temporary periods of disruption, persists for the lifetime of the animal. These movements serve to mix the ingesta, aid in eructation of gas, and propel fluid and fermented foodstuffs into the omasum. If motility is suppressed for a significant length of time, ruminal impaction may result. A cycle of contractions occurs 1 to 3 times per minute. The highest frequency is seen during feeding, and the lowest when the animal is resting. Two types of contractions are identified:
 

  Primary contractions originate in the reticulum and pass caudally around the rumen. This process involves a wave of contraction followed by a wave of relaxation, so as parts of the rumen are contracting, other sacs are dilating.
  • Secondary contractions occur in only parts of the rumen and are usually associated with eructation.
The animation below is based on data collected by radiographing sheep (Wyburn, 1980) and should impart at least some appreciation of the complexity of ruminal motility. Although shown much faster than in life, the major reticuloruminal contractions are timed appropriately. Note the movements which bring the gas bubble (stippled area) forward to the esophagus for eructation.






Saturday, April 12, 2008

How to Manage Feline Diabetics

How to Manage Feline Diabetics



PATHOPHYSIOLOGY OF DM
Diabetes mellitus (DM) is a common endocrine disease in cats characterized by an absolute or relative deficiency of insulin. This results in a decreased ability of cells to take up and utilize not only glucose, but also amino acids, fatty acids, and electrolytes. In addition the lack of insulin results in increased gluconeogenesis, glycogenolysis, lipolysis, ketogenesis, and protein catabolism. Predisposing factors in cats include obesity, advancing age, and being male.

Two types of DM are recognized in humans, and these classifications can be applied to the disease in cats. Type I DM (insulin dependent diabetes mellitus) is due to an absolute deficiency of insulin. This form of diabetes is characterized by minimal secretory response to ß-cell secretagogues such as glucagons. Type II DM (non-insulin dependent diabetes) is characterized by abnormal insulin secretion and peripheral insulin resistance, and results in a stable reregulation of the blood glucose concentration at a higher concentration. The two types of diabetes are classically distinguished by characteristic responses to challenge by insulin secretagogues such as glucose, glucagons, or arginine. In type I DM, there is a decreased or negligible secretion of insulin compared to normal animals, whereas in type II DM, total insulin secretion may be normal or increased, although the pattern of secretion may be abnormal. The insulin concentration is still insufficient, however, to prevent hyperglycemia. The phenomenon of glucose toxicity complicates interpretation of glucagon tolerance tests, particularly in cats, and the test is of little clinical utility. Currently the true prevalence of type I versus type II diabetes mellitus in diabetic cats is unknown.


DIAGNOSIS
The diagnosis of DM is made based on characteristic clinical signs of diabetes mellitus (polyuria, polydipsia, polyphagia, and weight loss), and documentation of hyperglycemia and glycosuria. In cats diagnosis may be complicated by the occurrence of marked stress hyperglycemia. When making a diagnosis of DM in cats, it is therefore important not only to document persistent hyperglycemia and glycosuria, but also to rule out other diseases that may cause similar clinical signs. Measurement of fructosamine concentration or urine glucose on urine samples collected in the home environment allow the clinician to distinguish between stress induced hyperglycemia (and resultant glycosuria) and persistent hyperglycemia due to diabetes mellitus. Glycosuria may also occur secondary to ketamine anesthesia, chronic renal failure, and postobstructive diuresis. The presence of significant ketonuria together with hyperglycemia, is diagnostic for diabetes mellitus in cats.

Cats are also unique in that DM may be transient or intermittent. In one study, 10 diabetic cats were reported to go into spontaneous remission after 1 to 3 months of therapy. In other studies, up to 70% of cats with DM have been reported to go into spontaneous clinical remission, suggesting that up to 70% of cats may have type II DM. The glucagon tolerance test is not useful in predicting whether or not a cat is likely to go into remission.


TREATMENT OF DIABETES MELLITUS IN CATS
Most diabetic cats should be treated with insulin in conjunction with dietary modification. Oral hypoglycemic drugs such as glipizide can be considered in certain circumstances but are not effective for control of diabetes mellitus in the majority of diabetic cats.


INSULIN
Insulins may be classified by insulin source, insulin formulation, or duration of action of insulin. Not all forms of insulin are currently commercially available and product availability is likely to continue to change. Insulin formulations that are or have been available in the recent past include:


short duration regular insulin (designated R)
moderate duration NPH insulin (designated N)
moderate duration Lente insulin (designated L)
long duration Ultralente insulin (designated U)
long duration PZI insulin.
Insulin may be derived from bovine, porcine, or human recombinant sources and the concentration may be either 100 units/mL or 40 units/mL. A number of human recombinant insulin analogues are also available.

The types of insulin recommended for use in cats have been complicated by the recent disappearance of many insulin products from the market. The insulin products that are currently available and recommended for use in small animals are listed below:


Short acting:
Regular insulin (Zinc insulin crystals)
Products: Humulin R [Lilly], Novolin R [NovoNordisk] Both human recombinant. 100 U/mL
Moderate acting:
NPH insulin (neutral protamine hagedorn) Complexed with protamine zinc in phosphate buffer
Products: (Humulin N [Lilly], Novolin N [NovoNordisk] Both human recombinant 100 U/mL
Lente insulin (3 parts semilente, seven parts ultralente)
Mix of crystalline and amorphous in acetate buffer
Products: Vetsulin [Intervet] Pure pork insulin (40 U/mL)
Long acting:
PZI insulin
Insulin complexed with protamine and zinc.
Products: PZI Vet, [Idexx] 90% Beef, 10% Pork (40 U/mL)
Glargine insulin long-acting insulin analog
Products: Lantus [Lilly] human recombinant. 100 U/mL

INSULIN THERAPY IN CATS
Regular insulin should be used in any sick or ketoacidotic patient for short term control of the blood glucose until the cat can be transitioned to a longer acting insulin. Insulin products suitable for long-term control of diabetes mellitus in cats include Lente, PZI, and Glargine insulin. NPH insulin, although it can be used in cats, is typically too short acting to result in good long-term glycemic control in most cats.


PZI Insulin
In a study of 67 diabetic cats (34 cats with newly diagnosed DM, and 33 cats with poorly controlled DM), PZI insulin was effective in decreasing BG concentration in 85% of cats and improving clinical signs in 90% of the cats within 45 days of initiating treatment. In this study all cats were treated with PZI twice daily, and the starting dose was 0.4 U/kg/injection. By the end of the study (day 45) the mean insulin dose was 0.9 U/kg/injection. The nadir of the blood glucose occurred at 5 to 7 hours post injection. Hypoglycemia occurred in 31% of the cats and sometimes occurred even when very low insulin doses were used. For this reason it is recommended that the starting insulin dose should be conservative (1 U/cat/injection) with subsequent dose increase made based upon response to treatment. It is important to note that this study used the commercially available PZI insulin (PZI Vet), not compounded PZI insulin, and similar results should not be expected with the products supplied by compounding pharmacies. Because PZI insulin has a well established track record in cats and a large prospective study on response to PZI insulin in cats has been published, PZI insulin is my first choice for treatment of diabetes mellitus in cats although this may change when more data is published on other insulin products in cats. The main disadvantage of PZI insulin is the expense ($82/vial, 20c/unit).


Pork Lente insulin (Vetsulin)
Lente insulin is also a suitable product for use in diabetic cats. Although it is not yet licensed in the US for cats it has been used successfully for years in cats in Europe. The major disadvantage of lente insulin is that it may be ineffective because of short duration of action in some cats. Unfortunately most studies of lente insulin in feline diabetics have used human recombinant insulin which is no longer available. The current lente insulin that is available is a pure pork insulin and the pharmacokinetics of this insulin may differ from that of human recombinant lente insulin. Useful information regarding use of vetsulin in cats . The starting dose for lente insulin in cats (0.25 - 0.5 U/kg/injection) is similar to that of other insulins. Lente insulin should be administered twice a day in cats. Lente insulin is considerably cheaper than PZI insulin (approximately $20/vial, 5c/unit).


Insulin Glargine
Early studies of the long-acting insulin analogue (insulin glargine) have been very promising. In a study of 13 diabetic cats treated with either once daily Glargine insulin at a dose of 0.5 U/kg once a day or lente insulin (human recombinant) 0.5 U/kg, twice a day, there was a significant improvement in both groups of cats and no difference between the two insulin groups. All cats were fed a commercial high protein low carbohydrate diet. Of the 4 cats in remission at the end of the study, 3 had been treated with lente insulin and one with glargine. In a study of 24 newly diagnosed diabetic cats, treated with either glargine, PZI, or lente, and fed a low carbohydrate high protein diet, glargine treated cats tended to have lower blood glucose concentrations and fructosamine concentrations than those treated with PZI or Lente. Glargine insulin resulted in higher remisison rates than did the cats treated with PZI or lente insulin. Despite these promising preliminary results further studies are necessary in larger numbers of diabetic cats. The cost of glargine insulin is approximately $65 /vial, 6.5 c/unit).


General Recommendations for Insulin Treatment in Cats
The starting dose for insulin in a new feline diabetic patient is 0.25 - 0.5 U/kg or 1 - 3 U/cat. It is recommended that PZI insulin should be started at the lower end of this dose.

It is difficult to predict in advance which cats will do better with which insulin formulation. The potency of different insulin formulations may vary from cat to cat, but this is not usually predictable in an individual animal, although longer acting insulins as a rule are less potent than shorter acting insulin. It is therefore important that a blood glucose curve is performed within 5 - 7 days of making any change in insulin formulation. Cats should also be carefully monitored for clinical signs of hypoglycemia, because of the possibility of remission of diabetes mellitus in the cat. Whatever insulin formulation is chosen, twice a day insulin therapy is most likely to result in ideal glycemic control. If this is not possible, once a day therapy with PZI Vet or glargine can result in effective control of clinical signs.


Switching from One Insulin Product to Another
The first step is to evaluate how well regulated the animal is on the current insulin product. Next the clinician should determine the potency of of the new insulin versus old insulin (long acting insulins are less potent than moderate acting insulins). Finally the proposed frequency of administration of the new insulin should be determined. In general better glycemic control can be established in cats (and the likelihood of remission increased) by using twice a day insulin. The new dose should then be determined based on these factors: If animal has good glycemic regulation, if switching to a more potent insulin or increasing the frequency of administration the dose should be decreased by 10 - 25%. If current glycemic control is poor and the potency of the new insulin is the same or less keep the same dose. The final dose should be adjusted based on clinical response, blood glucose curve concentrations (at least 5 - 7 days after the change in insulin formulation), and measurement of fructosamine (2 - 4 weeks after the change in insulin formulation). When switching insulins it is important to educate owners about obtaining and using U40 insulin syringes if you are switching to Vetsulin or PZI Vet. It is NOT recommended to use U100 syringes with U40 insulin by making a dose adjustment. This is liable to lead to serious dosage errors. The owner should also be educated about the clinical signs of hypo-and hyperglycemia, and taught how to manage an episode of suspected hypoglycemia.


DIETARY MANAGEMENT
Dietary management is an important adjunct therapy in management of diabetic cats. Options include a high fiber, moderate carbohydrate and fat diet; or a low carbohydrate/high protein diet; both types of diets have been demonstrated to improve glycemic control in feline diabetic patients. A prospective study comparing a low carbohydrate-low fiber diet to a moderate carbohydrate-high fiber diet in 63 diabetic cats showed improvements in glycemic control in both groups, but there was a higher rate of remission of diabetes mellitus in the low carbohydrate-low fiber diet. These findings support the clinical opinion that low carbohydrate diets in conjunction with good glycemic control increase the likelihood of diabetic remission. Which diet will be the most effective in improving glycemic control in individual patients is unpredictable, although it makes clinical sense to start with a low carbohydrate diet in most cats, and move to a high fiber diet if clinical remission is not achieved with the low carbohydrate diet and better glycemic control is needed. Other factors such as bodyweight of the cat, other concurrent diseases, and diet palatability should also be considered when choosing a diet for a diabetic cat.


POOR RESPONSE TO INSULIN
Clinical signs suggestive of inappropriate response to insulin therapy include recurrence or persistence of clinical signs of DM, disorientation or seizures due to hypoglycemia, or an insulin dose higher than 6U/injection in the cat. Adequate assessment of the cause of the problem requires performing a blood glucose curve. Measurement of fructosamine concentration may also be helpful. In cats receiving twice-daily insulin, most glucose curves can be performed during working hours (8 AM to 6 PM). Based on the results of the blood glucose curve and fructosamine concentration, appropriate recommendations for changes in treatment or further diagnostic testing can then be made. Common problems that may lead to a poor response to insulin include problems with owner administration, inappropriate insulin dose or formulation, insulin induced hypoglycemia, rapid metabolism of insulin, and insulin resistance. It is important , when interpreting the results of blood glucose curves to take into consideration the level of stress of the patient while in the hospital. Other factors such as clinical signs, results of urine blood glucose measurements at home, serum fructosamine concentrations, and changes in physical examination (especially body weight), should be taken into account when interpreting the blood glucose curves.
Wednesday, March 12, 2008