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Topic:Intravenous Administration

Intravenous administration in horses involves the delivery of substances directly into the bloodstream through a vein. This method is used to administer fluids, medications, and nutrients efficiently, ensuring rapid distribution throughout the body. It is commonly employed in veterinary practice for rehydration, anesthesia, and treatment of various medical conditions. The technique requires skill and knowledge to ensure proper vein selection and catheter placement, minimizing the risk of complications such as infection or thrombosis. This page compiles peer-reviewed research studies and scholarly articles that explore the methodologies, applications, and potential complications associated with intravenous administration in equine medicine.
[The use of amikacin in the treatment of endometritis caused by Pseudomonas aeruginosa in mares].
Journal of the South African Veterinary Association    June 1, 1982   Volume 53, Issue 2 124-126 
van Dyk E, Immelman A, van Heerden JS.After isolation of Pseudomonas aeruginosa from endometrial biopsies of 6 mares they were treated with amikacin sulphate. Three were treated by intra-uterine application of the drug, in one the drug was given by intramuscular injection, in another the intravenous route was used while in the last mare simultaneous local and intravenous treatment was applied. An intra-uterine Tris-EDTA instillation preceeded the uterine amikacin instillations to aid in the breakdown of the capsule around the bacterium. Serum concentrations of amikacin were determined after intravenous and intramuscular administra...
Effect of glucose administration on equine fasting hyperbilirubinemia.
American journal of veterinary research    May 1, 1982   Volume 43, Issue 5 801-803 
Gronwall R, Engelking LR.The effects of several treatments and their routes of administration on the reduction of hyperbilirubinemia in 9 pony mares after a 3-day fast were studied. Treatments were as follows: glucose given at doses of 1.2, 2.4, and 3.7 mg/min/kg of body weight; refeeding the base-line diet; feeding straw; and IV administration of taurocholic acid at a dosage of 0.07 mumol/min/kg. The 3 glucose dosages were each given by 3 different routes: IV, intraduodenal, and intragastric. The smallest dosage of glucose given by IV route reduced the plasma bilirubin concentration only 7%, even though other measure...
The pharmacokinetics, pharmacological responses and behavioral effects of acepromazine in the horse.
Journal of veterinary pharmacology and therapeutics    March 1, 1982   Volume 5, Issue 1 21-31 doi: 10.1111/j.1365-2885.1982.tb00495.x
Ballard S, Shults T, Kownacki AA, Blake JW, Tobin T.After intravenous (i.v.) injection, acepromazine was distributed widely in the horse (Vd = 6.6 litres/kg) and bound extensively (greater than 99%) plasma proteins. Plasma levels of drug declined with an alpha half-life of 4.2 min, while the beta phase or elimination half-life was 184.8 min. At a dosage level of 0.3 mg/kg acepromazine was detectable in the plasma for 8 h post dosing. The whole blood partitioning of acepromazine was 46% in the plasma phase and 54% in the erythrocyte phase. Penile prolapse was clearly evident at doses from 0.01 mg/kg to 0.4 mg/kg i.v., and the duration and extent...
Effects of enkephalins versus opiates on locomotor activity of the horse.
Research communications in chemical pathology and pharmacology    March 1, 1982   Volume 35, Issue 3 405-419 
Nugent TE, Combie JD, Weld JM, Burns P, Tobin T.The enkephalins are small, pentapeptide neurotransmitter molecules which have reportedly been used in racing horses. In our experiments, D-Ala2-Metenkephalinamide and leucine enkephalin were administered to horses intravenously (IV) and intracisternally (IC). Leucine enkephalin had little effect on locomotor activity by either route at doses of 0.01 mg/Kg or less. Methionine enkephalinamide, an enzyme resistant enkephalin analog, had no significant effect when given IV (0.002 and 0.008 mg/kg). Other experiments involving intracisternal dosing with this long acting form at higher levels (0.005-...
[Ascorbic acid status of horses. 4. Behavior of serum levels following intravenous administration].
Berliner und Munchener tierarztliche Wochenschrift    February 15, 1982   Volume 95, Issue 4 71-76 
Jaeschke G, Keller H.No abstract available
Plasma and tissue concentrations of oxytetracycline in the horse after intravenous administration.
American journal of veterinary research    December 1, 1981   Volume 42, Issue 12 2165-2166 
Larson VL, Stowe CM.Oxytetracycline (OTC) was administered IV to 3 clinically normal horses at a dosage of 10 mg of OTC/kg of body weight. Plasma OTC concentrations were determined at 30-minute intervals until postinjection minute (PIM) 240. At PIM 240, the mean OTC concentration in pulmonary tissue was 3.96 microgram/g of tissue (wet weight) and in renal tissue was 25.47 micrograms/g. diluted bronchial fluid had a mean concentration of 0.288 microgram of OTC/ml at PIM 240. The data demonstrated that OTC has adequate tissue distribution in horses.
The pharmacokinetics of some aminoglycoside antibiotics in the horse.
Journal of veterinary pharmacology and therapeutics    December 1, 1981   Volume 4, Issue 4 277-284 doi: 10.1111/j.1365-2885.1981.tb00863.x
Baggot JD, Love DN, Rose RJ, Raus J.The disposition kinetics and bioavailability of streptomycin, kanamycin and neomycin were determined following their administration as parenteral preparations to horses. Single doses (10 mg/kg) of each aminoglycoside were given by the intravenous (i.v.) and intramuscular (i.m.) routes and, at a later time, seven intramuscular doses were injected at 12-h intervals. The pharmacokinetic behaviour of the three aminoglycosides was similar, in that a rapid distribution phase was followed by a relatively short half-life. The half-life (mean +/- SD, n = 6) of kanamycin (1.80 +/- 0.17 h) was significan...
Intravenous catheterisation of the horse.
In practice    September 1, 1981   Volume 3, Issue 5 20-23 doi: 10.1136/inpract.3.5.20
Urquhart K.No abstract available
Pharmacokinetic analysis of intravenously and orally administered quinidine in horses.
American journal of veterinary research    June 1, 1981   Volume 42, Issue 6 938-942 
McGuirk SM, Muir WW, Sams RA.A pharmacokinetic study was made, using 7 healthy adult horses (weighing between 400 and 560 kg) given quinidine gluconate IV and quinidine sulfate orally. The apparent volume of distribution of quinidine base was 3.10 +/- 0.79 L/kg, total body clearance was 5.49 +/- 2.40 ml/minute/kg, and plasma half-life was 6.65 +/- 3.00 hours. The systemic availability of quinidine sulfate after oral administration of a 10 mg/kg dose was 48.5 +/- 20.4%. Oral administrations of quinidine sulfate in doses of 10 mg/kg and 10 g produced peak plasma concentrations of 0.79 microgram/ml at 146 minutes and 1.47 mi...
Blood flow in the hypertrophied right ventricular myocardium of unanesthetized ponies.
The American journal of physiology    June 1, 1981   Volume 240, Issue 6 H881-H888 doi: 10.1152/ajpheart.1981.240.6.H881
Manohar M, Bisgard GE, Bullard V, Rankin JH.To examine the effects of right ventricular (RV) hypertrophy on regional myocardial blood flow and coronary vascular reserve, hemodynamics and myocardial blood flow (15-micrometers radio-nuclide-labeled microspheres) were studied in 12 unanesthetized adult ponies before and during intravenous isoproterenol HCl infusion (1 microgram.kg-1.min-1). Six ponies served as controls, whereas in each of the others the main pulmonary artery (PA) had been banded 35-90 days prior to the study. Marked RV hypertrophy was present in PA-banded animals. In these ponies, there was a significant increase in RV sy...
The pharmacokinetics of xylazine hydrochloride: an interspecific study.
Journal of veterinary pharmacology and therapeutics    June 1, 1981   Volume 4, Issue 2 87-92 doi: 10.1111/j.1365-2885.1981.tb00715.x
Garcia-Villar R, Toutain PL, Alvinerie M, Ruckebusch Y.The pharmacokinetic disposition of xylazine hydrochloride is described after both intravenous and intramuscular injection of a single dose, in four domestic species: horse, cattle, sheep and dog, by an original high performance liquid chromatographic technique. Remarkably small interspecific differences are reported. After intravenous administration, systemic half-life (t1/2 beta) ranged between 22 min (sheep) and 50 min (horse) while the distribution phase is transient with half-life (t1/2 alpha) ranging from 1.2 min (cattle) to 5.9 min (horse). The peak level of drug concentration in the pla...
The pharmacokinetics of meclofenamic acid in the horse.
Journal of veterinary pharmacology and therapeutics    June 1, 1981   Volume 4, Issue 2 147-156 doi: 10.1111/j.1365-2885.1981.tb00724.x
Snow DH, Baxter P, Whiting B.The pharmacokinetics of meclofenamic acid were studied in Thoroughbred horses and in ponies. After intravenous (i.v.) administration of either 2 mg/kg or 4 mg/kg sodium meclofenamate the elimination half-life was of the order of 0.9 h while the volume of distribution was found to be 0.128 litre/kg. Elimination was in accordance with a one-compartment model. Following oral administration of either meclofenamic acid (4 mg/kg) or sodium meclofenamate (4 mg/kg) a much longer terminal half-life than that calculated for Kel from i.v. data was found. This anomaly indicated that the 'flip-flop' phenom...
Intravenous anesthesia: drugs and techniques.
The Veterinary clinics of North America. Large animal practice    May 1, 1981   Volume 3, Issue 1 195-208 doi: 10.1016/s0196-9846(17)30152-0
Short CE.No abstract available
Pharmacokinetics and behavioral effects of methylphenidate in Thoroughbred horses.
American journal of veterinary research    May 1, 1981   Volume 42, Issue 5 722-726 
Shults T, Kownacki AA, Woods WE, Valentine R, Dougherty J, Tobin T.In horses given (rapid IV) methylphenidate (Ritalin, alpha-phenyl-2-piperidinacetic acid methyl ester; 0.70 mg/kg), plasma concentrations of the drug decreased rapidly at first, with an apparent alpha half-life of about 19 minutes, and then more slowly, with an apparent beta half-life of about 2.4 hours. These data were well fitted by a 2-compartment open model. In blood, about 40% of the methylphenidate present was in the plasma fraction, and of this, about 80% was plasma-protein bound. If given by subcutaneous or IM injection, plasma concentrations of methylphenidate peaked in about 1 hour a...
Effects of xylazine and ketamine hydrochloride on the electroencephalogram and the electrocardiogram in the horse.
American journal of veterinary research    April 1, 1981   Volume 42, Issue 4 615-619 
Purohit RC, Mysinger PW, Redding RW.A continuous series of electroencephalograms (EEG) was obtained from each of 6 mature horses which had been given xylazine and ketamine hydrochloride IV. Electrocardiograms and respiratory rates were also obtained. The EEG of the unsedated standing adult horse displayed a dominant fast activity in the range of 25-35 Hz, 5-30 microV superimposed over slower 1-4 Hz, 10-50 microV activity with occasional 10-14 Hz, 10-40 microV spindle-type activity. The xylazine-sedated horse displayed hypersynchronous EEG patterns, with the dominant activity being 1-3 Hz, 10-70 microV with overlying mixed freque...
Dose-response of ponies to parenteral Escherichia coli endotoxin.
Canadian journal of comparative medicine : Revue canadienne de medecine comparee    April 1, 1981   Volume 45, Issue 2 207-210 
Burrows GE.The response of the pony to increasing doses of Escherichia coli endotoxin was evaluated using intravenous and intraperitoneal administration models. Marked changes were seen in all parameters measured following endotoxin administration. Leukopenia (neutropenia, lymphopenia) and thrombocytopenia were not dose-dependent. Similarly, elevated plasma fibrinogen and altered glucose concentrations (hyperglycemia and hypoglycemia), pyrexia and increased lactate/pyruvate ratios were apparent at all endotoxin doses but were not dose related. The widely used packed cell volume and capillary refill time,...
Oxytetracycline hydrochloride in the horse: serum, synovial, peritoneal and urine concentrations after single dose intravenous administration.
Journal of veterinary pharmacology and therapeutics    March 1, 1981   Volume 4, Issue 1 7-10 doi: 10.1111/j.1365-2885.1981.tb00703.x
Brown MP, Stover SM, Kelly RH, Farver TB, Knight HD.Six adult mares were given a single intravenous injection of oxytetracycline HCl (50 mg/ml) at a dosage of 5 mg/kg. Serum, synovial fluid, peritoneal fluid, and urine oxytetracycline concentrations were measured serially over a 48-h period. The highest measured serum oxytetracycline concentration was 8.01 mcg/ml at 1/2 h. Oxytetracycline was detected in synovial fluid and peritoneal fluid, which obtained mean peak oxytetracycline concentrations of 4.43 mcg/ml and 4.20 mcg/ml, at 1/2 h and 1 h, respectively. These concentrations steadily declined in parallel with serum concentrations and were n...
Cardiopulmonary effects of clenbuterol in the horse.
Journal of veterinary pharmacology and therapeutics    March 1, 1981   Volume 4, Issue 1 43-50 doi: 10.1111/j.1365-2885.1981.tb00709.x
Shapland JE, Garner HE, Hatfield DG.Clenbuterol, a bronchospasmolytic agent (beta 2 agonist) was studied in terms of its hemodynamic and airflow response in eight, healthy horses. Four animals were instrumented to record intrapleural pressure and air flow, these were used to compute pulmonary resistance, peak flow rates, and tidal volumes. Four animals were instrumented to record pulmonary arterial pressure, carotid arterial pressure, cardiac output, and arterial gas tensions. After control values were recorded, clenbuterol (0.8 microgram/kg) was intravenously administered to each horse in each experiment group. Following clenbu...
Clinicopathologic effects of rapid infusion of 5% sodium bicarbonate in 5% dextrose in the horse.
Journal of the American Veterinary Medical Association    February 1, 1981   Volume 178, Issue 3 267-271 
Rumbaugh GE, Carlson GP, Harrold D.Clinicopathologic effects of rapid intravenous infusion of 3 L of 5% dextrose in water containing 150 g of sodium bicarbonate were evaluated in 8 clinically normal horses. A highly significant metabolic alkalosis was produced in all the horses. This response was maximal at the end of the 20-minute infusion but persisted for as long as 8 hours. Packed cell volume, total plasma proteins, plasma potassium, and plasma chloride concentration decreased significantly after infusion, while plasma sodium concentration increased significantly. The clinical and clinicopathological responses of the horses...
Systemic and digital vascular effects of intravenous histamine in the pony.
American journal of veterinary research    February 1, 1981   Volume 42, Issue 2 205-208 
Robinson NE, Scott JB.The effects of a 60-minute IV infusion of histamine (0.5 mg of histamine base/minute) on the systemic, pulmonary, and digital vasculature were investigated in mature ponies. Immediately after the start of histamine infusion, there were a transient decrease in systemic pressure lasting less than 1 minute and then a brief period of systemic hypertension. Systemic pressure then returned to preinfusion levels for the remainder of the infusion period. Pulmonary arterial pressure increased transiently coincident with systemic hypotension. Histamine increased cardiac output and decreased both total p...
Evaluation of an intravenous catheter for use in the horse.
Journal of the American Veterinary Medical Association    February 1, 1981   Volume 178, Issue 3 272-273 
Gulick BA, Meagher DM.A commercially available polyvinyl chloride intravenous catheter was studied in 9 horses for 3 to 10 days to evaluate the catheter's suitability for use in the horse, to develop a new insertion technique, and to establish a protocol for catheter care. Seven of the animals were clinically normal horses receiving parenteral nutrition; one was a horse with hypocalcemia receiving frequent intravenous injections of calcium gluconate, and one was a clinically normal horse receiving no infusions. The catheter dressings were changed every 48 hours, and an aspirate from the catheter and the catheter ti...
[Practolol test for adrenergic beta receptor blockade in veterinary electrocardiographic diagnosis].
Polskie archiwum weterynaryjne    January 1, 1981   Volume 23, Issue 1 95-101 
Grodzki K.The receptor theory of the action of catecholamines as well as the synthesis and production of beta-adrenolytics gave new perspectives for the treatment of circulatory diseases and enabled to use the beta-adrenergic blockade in electrocardiographic diagnosis. The aim of this work was to study whether it is possible to modify the oral method of administration used in human beings, into intravenous one, and what an information could be obtained as to actual heart condition after practolol injection. The results can be summarized as follows:--Practolol-Polfa injected intravenously in amounts of 3...
The metabolism of promazine and acetylpromazine in the horse.
Drug metabolism and disposition: the biological fate of chemicals    January 1, 1981   Volume 9, Issue 1 30-36 
Dewey EA, Maylin GA, Ebel JG, Henion JD.Promazine hydrochloride and acetylpromazine maleate were administered intravenously at clinical dose levels to horses. In urine from horses given promazine hydrochloride, the parent drug and four metabolites were detected. The two major metabolites, present as conjugates were identified after hydrolysis by beta-glucuronidase/arylsulfatase as 3-hydroxypromazine and 3-hydroxydesmonomethyl-promazine. Conjugated 3-hydroxypromazine has been previously identified as a major metabolite in the horse. Two minor metabolites isolated in this study were primaizine N-oxide and promazine N-oxide sulfoxide. ...
Therapeutic effect of phenylbutazone on experimental acute Escherichia coli endotoxemia in ponies.
American journal of veterinary research    January 1, 1981   Volume 42, Issue 1 94-99 
Burrows GE.Phenylbutazone (PBZ), a classic anti-inflammatory and prostaglandin-synthesis inhibitor drug, was used to determine the role of prostaglandins and other mediators on the development and perpetuation of the response to intraperitoneal Escherichia coli endotoxin administration. The PBZ (15 mg/kg of body weight) was administered IV 30 minutes after endotoxin administration and was repeated later at 6 and 12 hours at a dose of 10 mg/kg. A variety of evaluation measurements (hematologic, blood glucose, pyruvate, lactate and fibrinogen, serum beta-glucuronidase, prothrombin time, blood gases, hepati...
Intravenous anaesthesia in horses after xylazine premedication.
The Veterinary record    September 13, 1980   Volume 107, Issue 11 241-245 doi: 10.1136/vr.107.11.241
Brouwer GJ, Hall LW, Kuchel TR.The effects of combining large doses of xylazine (1.1 mg per kg intravenously) with ketamine, methohexitone and thiopentone were studied in four experimental ponies. Onset of anaesthesia was more delayed after ketamine than after the barbiturates. Assessment of smoothness of induction and recovery indicated that all three combinations were effective and acceptable. Injection of xylazine was followed by atrioventricular (A-V) block which could be prevented by the prior administration of atropine. Blood pressure was well maintained with all three combinations of drugs. Arterial oxygen tension de...
Digoxin pharmacokinetics, bioavailability, efficacy, and dosage regimens in the horse.
American journal of veterinary research    September 1, 1980   Volume 41, Issue 9 1388-1395 
Button C, Gross DR, Johnston JT, Yakatan GJ.The pharmacokinetics of IV administered digoxin and the bioavailability of intragastrically administered powdered digoxin tables suspended in water were investigated in 6 clinically normal adult horses by 125I radioimmunoassay. The effect of 3 to 5 sequential IV doses of 5 micrograms of digoxin/kg of body weight at 2-hour intervals on a left ventricular index of contractility (Vmax) was assessed in 5 clinically normal horses. Standard pharmacokinetic equations and mean pharmacokinetic variables were used to derive parenteral and oral (loading and maintenance) doses for digoxin in horses. The c...
Induced juglone toxicosis in ponies and horses.
American journal of veterinary research    June 1, 1980   Volume 41, Issue 6 944-945 
True RG, Lowe JE.Juglone, a toxic compound found in all parts of plants of the walnut tree family Jugans, was evaluated as the possible toxin involved in black walnut shaving-associated laminitis in the horse. Large amounts (up to 1 g) of this chemical administered per os inconsistently caused mild signs of laminitis in ponies. Topical application of juglone to the digits of horses caused local skin irritation but did not cause laminitis. Intravenous administration of juglone caused acute pulmonary edema in some individuals previously exposed to the compound per os or IV.
A freeze-thaw method for concentrating plasma and serum for treatment of hypogammaglobulinaemia.
The Australian journal of experimental biology and medical science    April 1, 1980   Volume 58, Issue 2 133-142 doi: 10.1038/icb.1980.13
Thomas KW, Pemberton DH.Components of plasma or serum, including immunoglobulins, were concentrated two-fold by freezing then collecting 40-50% of the initial volume during thawing. This concentrated plasma (or serum) was administered intravenously to treat hypogammaglobulinaemic foals and calves. An adaptation of this method suitable for field use is described.
Low doses of oxytocin can induce foaling at term.
Equine veterinary journal    April 1, 1980   Volume 12, Issue 2 85-87 doi: 10.1111/j.2042-3306.1980.tb02316.x
Pashen RL.Levels of the major circulating metabolite of prostaglandin F-2 alpha, 13, 14 dihydro-15-oxo-prostaglandin F-2 alpha (PGFM) were measured during the induction of foaling using small (2.5-10 iu) intravenous doses of oxytocin. PGFM levels rose rapidly in all animals within 15 min of injection and were associated with typical signs of second stage labour. Because these small doses of oxytocin are effective in successfully triggering parturition it is suggested that higher doses (40-120 iu) used to induce birth in other studies are unnecessary and could be potentially dangerous to the foetal foal....
Pharmacokinetics of gentamicin in the horse.
American journal of veterinary research    March 1, 1980   Volume 41, Issue 3 351-354 
Pedersoli WM, Belmonte A, Purohit RC, Ravis WR.The pharmacokinetics of gentamicin were studied in six healthy mature horses of mixed breeding and of both sexes. A parenteral preparation of gentamicin sulfate (5% aqueous solution) was administered rapidly (IV) at the dosage level of 5 mg/kg of body weight. Venous blood samples were taken at 0 (base line), 0.083, 0.25, 0.5, 0.75, 1, 2, 4, 8, 12, 24, 36, 48, 72, 96, and 120 hours after gentamicin administration. Serum gentamicin was measured by a radioimmunoassay technique. The gentamicin concentration data was fitted to a one- and two-compartment open model with first-order elimination from ...