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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 pharmacology of furosemide in the horse. V. Pharmacokinetics and blood levels of furosemide after intravenous administration.
Drug metabolism and disposition: the biological fate of chemicals    May 1, 1983   Volume 11, Issue 3 226-231 
Chay S, Woods WE, Rowse K, Nugent TE, Blake JW, Tobin T.Studies were undertaken to determine blood levels of furosemide in horses after 0.5- and 1.0-mg/kg doses administered iv. Analyses indicated that the pharmacokinetic parameters were dose independent and best described by a three-compartment open model. The alpha-, beta-, and gamma-phase half-lives of 5.6, 22.3, and 158.5 min, respectively, were observed after the 0.5-mg/kg dose. Similarly, the respective half-lives after the 1.0-mg/kg dose were 5.8, 24.1, and 177.2 min. After a 0.5-mg/kg dose of furosemide, population frequency distributions were evaluated at 1 hr and 4 hr post-drug administra...
Trimethoprim-sulfadiazine in the horse: serum, synovial, peritoneal, and urine concentrations after single-dose intravenous administration.
American journal of veterinary research    April 1, 1983   Volume 44, Issue 4 540-543 
Brown MP, Kelly RH, Stover SM, Gronwall R.Six healthy adult mares were given a single IV injection of trimethoprim (TMP)-sulfadiazine (SDZ) at a dosage rate of 2.5 mg of TMP/kg of body weight and 12.5 mg of SDZ/kg. Serum, synovial, peritoneal, and urine TMP-SDZ concentrations were measured serially over a 48-hour period. The highest measured mean concentrations of TMP and SDZ were found in the first (0.5 hour) sample of serum, synovial fluid, and peritoneal fluid. The mean peak concentrations of TMP and SDZ averaged 4.37 micrograms/ml and 21.81 micrograms/ml for serum, 2.95 micrograms/ml and 15.31 micrograms/ml for synovial fluid, and...
Pharmacokinetics of erythromycin in foals and in adult horses.
Journal of veterinary pharmacology and therapeutics    March 1, 1983   Volume 6, Issue 1 67-73 doi: 10.1111/j.1365-2885.1983.tb00456.x
Prescott JF, Hoover DJ, Dohoo IR.The pharmacokinetic parameters of erythromycin in foals were determined following intravenous administration of 5.0 mg/kg to animals aged 1, 3, 5 and 7 weeks. The distribution of the drug was described by a two-compartment open model, and no significant differences were observed between coefficients on which the parameters were based. Pharmacokinetic values were also determined for four mares given 5.0 mg/kg intravenously and for six 10-12-week-old foals given 20.0 mg/kg intravenously. The half-life of erythromycin for all groups of animals (foals less than 7 weeks, mares, foals 10-12 weeks) w...
Decreased tear production associated with general anesthesia in the horse.
Journal of the American Veterinary Medical Association    February 1, 1983   Volume 182, Issue 3 243-244 
Brightman AH, Manning JP, Benson GJ, Musselman EE.Schirmer I tear tests were conducted on 14 horses. The test was performed before and after IV administration of xylazine hydrochloride, during maintenance anesthesia with halothane in oxygen, and 3 hours after discontinuation of anesthesia. Xylazine hydrochloride did not decrease tear production from the mean base-line value of 23.94 +/- 5.23 mm/min after its IV administration. Tear production was decreased to mean values of 15.57 +/- 4.29 mm/min at 30 minutes and 13.84 +/- 4.25 mm/min at 60 minutes during the maintenance of halothane anesthesia. Three hours after anesthesia was discontinued, ...
Review of 30 cases of peritonitis in the horse.
Equine veterinary journal    January 1, 1983   Volume 15, Issue 1 25-30 doi: 10.1111/j.2042-3306.1983.tb01693.x
Dyson S.Thirty cases of peritonitis, in which the diagnosis was based on a peritoneal fluid white blood cell count in excess of 10 x 10(9)/litre, are described. Colic, ileus, pyrexia, weight loss and diarrhoea were common presenting signs. Treatments included intravenous fluids, anti-inflammatory analgesics, broad spectrum antibiotics and anthelmintics. Duration of treatment was determined by the clinical condition of the horse and sequential analyses of the peritoneal fluid and the haemogram. In the majority of cases the primary cause of peritonitis was not accurately determined, but 21 horses (70 pe...
Pharmacology, pharmacokinetics, and behavioral effects of caffeine in horses.
American journal of veterinary research    January 1, 1983   Volume 44, Issue 1 57-63 
Greene EW, Woods WE, Tobin T.Caffeine (4 mg/kg) was given by rapid IV injection to 4 horses. Plasma concentrations of the drug peaked at 10 micrograms/ml and decreased rapidly at first, and then more slowly, with an apparent beta-phase half-life of 18.2 hours. Urinary concentrations of caffeine were remarkably consistent at about 3 times plasma values of the drug. Caffeine was detectable in both plasma and urine of the horses for up to 9 days after dosing. After oral administration, caffeine was absorbed poorly with an apparent bioavailability of 39%. Although blood concentrations of caffeine peaked rapidly after oral adm...
Serum concentrations of penicillin in the horse after administration of a variety of penicillin preparations.
Equine veterinary journal    January 1, 1983   Volume 15, Issue 1 43-48 doi: 10.1111/j.2042-3306.1983.tb01700.x
Love DN, Rose RJ, Martin IC, Bailey M.Twelve geldings were used to evaluate serum levels of penicillin following the intravenous (iv) and intramuscular (im) injection of benzylpenicillin, im procaine penicillin and im fortified benzathine penicillin, at a variety of dose rates. Blood samples were collected up to 7 h after iv and im benzylpenicillin, up to benzathine penicillin. Results were analysed using an analysis of variance and regression analyses were used to calculate the time taken for the serum penicillin concentration to decline to 0.5 micrograms/ml. As a result of the experiments the following dosage regimes could be re...
[Experimental reproduction of lactic acidosis in the pony].
Annales de recherches veterinaires. Annals of veterinary research    January 1, 1983   Volume 14, Issue 3 195-206 
Wolter R, Durix A, Letourneau JC, Carcelen M, Henry N.One pony has been subjected to the intravenous injections of L-lactic acid. Two other ponies have been trained to intracaecal administration of L-lactic acid or sucrose. The obtained results show that: Intravenous injection of lactic acid increases the concentration of histamin and lactic acid, decreases the level of magnesium and reduces the pressure of carbon dioxide in the blood (the control animals and the treated animals) without the clinical symptoms of lactic acidosis. Intracaecal administration of lactic acid induces a high liberation of histamin in the caecum (the control animals and ...
Xylazine hydrochloride-induced hyperglycemia and hypoinsulinemia in thoroughbred horses.
Journal of veterinary pharmacology and therapeutics    December 1, 1982   Volume 5, Issue 4 241-245 doi: 10.1111/j.1365-2885.1982.tb00439.x
Thurmon JC, Neff-Davis C, Davis LE, Stoker RA, Benson GJ, Lock TF.The effects of intravenous xylazine (1.1 mg/kg) were studied in six thoroughbred horses (five mares and a stallion). Plasma glucose concentration increased to 168% of control at 45 min and decreased to 112% of control at 180 min. Insulin had decreased to 31% of control at 15 min. Thereafter, insulin concentration increased, reaching its highest concentration at 150 min. The mechanism for these changes is not fully understood and further investigation is indicated.
Pulmonary effects of intravenous histamine in the conscious pony: dose-response relationships and reproducibility.
American journal of veterinary research    December 1, 1982   Volume 43, Issue 12 2134-2137 
Derksen FJ, Slocombe RF, Robinson NE.In standing sedated ponies, we measured dynamic lung compliance (Cdyn) and pulmonary resistance (RL) during IV infusion of various doses of histamine; this was done in a given pony 3 times at 1-week intervals between experiments. Histamine doses causing a decrease in Cdyn of 50% and 75% and an increase in RL of 300% and 600% (ED50Cdyn, ED75Cdyn, ED300RL and ED600RL, respectively) were interpolated from the histamine dose-response curves. We also measured respiratory frequency, tidal volume, minute ventilation, functional residual capacity, arterial oxygen tension, arterial carbon dioxide tensi...
Electrocardiographic changes in induced hyperkalemia in ponies.
American journal of veterinary research    November 1, 1982   Volume 43, Issue 11 1934-1937 
Glazier DB, Littledike ET, Evans RD.In 11 crossbred ponies, hyperkalemia was induced by acute intracardiac infusion of a 0.4M solution of potassium chloride. The ECG changes noticed can be assigned to 4 stages: (1) a widening and a lowering of amplitude followed by inversion and final disappearance of the P wave; (2) an increase in the amplitude of the T wave; (3) an increase in the QRS interval, with some irregularity in the ventricular rate; and (4) periods of cardiac arrest that became terminal or were followed by ventricular fibrillation. At plasma potassium values of greater than 7.5 mM/L, the T-wave amplitude and duration ...
Hypotension in the horse induced by acepromazine maleate.
Australian veterinary journal    November 1, 1982   Volume 59, Issue 5 148-152 doi: 10.1111/j.1751-0813.1982.tb02761.x
Parry BW, Anderson GA, Gay CC.The hypotensive effect of acepromazine maleate was related to both the dose and route of administration. The degree and duration of hypotension varied between individual horses. In general, intravenous administration produced a more rapid maximum effect than intramuscular injection and the larger the dose the longer blood pressure remained at low levels. Average systolic pressure (of 6 horses) remained significantly below control values for more than 6 h after an intramuscular injection of 0.05 mg acepromazine maleate/kg body weight. Respiratory rate was markedly decreased, with the duration, ...
Pharmacodynamic and pharmacokinetic properties of diazepam in horses.
American journal of veterinary research    October 1, 1982   Volume 43, Issue 10 1756-1762 
Muir WW, Sams RA, Huffman RH, Noonan JS.The cardiopulmonary, behavioral, and pharmacokinetic properties of diazepam were determined in horses. Heart rate, cardiac output, mean pulmonary artery, aortic and right atrial blood pressures, respiratory rate, and arterial pH and blood gas values did not change after IV diazepam (0.05, 0.1, 0.2, 0.4 mg/kg) administration. Increasing doses of diazepam resulted in signs of muscle weakness including fixed stance, muscle fasciculations of the head, neck, and thorax muscles, ataxia, and then recumbency. Dosages of diazepam exceeding 0.2 mg/kg produced mild sedation. Behavioral changes persisted ...
The effect of ethacrynic acid, bumetanide, frusemide, spironolactone and ADH on electrolyte excretion in ponies.
Journal of veterinary pharmacology and therapeutics    September 1, 1982   Volume 5, Issue 3 153-160 doi: 10.1111/j.1365-2885.1982.tb00426.x
Alexander F.The effect of ethacrynic acid, bumetanide, frusemide, spironolactone and anti-diuretic hormone (ADH) on the urinary and faecal excretion of water and electrolytes by ponies was studied. Ethacrynic acid, bumetanide, and frusemide given intravenously, increased urinary sodium excretion, and, excepting frusemide, decreased faecal sodium excretion. Given by stomach tube ethacrynic acid reduced urinary and faecal sodium. Bumetanide, given intravenously, spironolactone, frusemide and ADH increased urinary sodium and all except frusemide intravenously decreased faecal sodium regardless of route of ad...
Bioavailability of phenylbutazone preparations in the horse.
Equine veterinary journal    July 1, 1982   Volume 14, Issue 3 234-237 doi: 10.1111/j.2042-3306.1982.tb02404.x
Rose RJ, Kohnke JR, Baggot JD.Plasma phenylbutazone concentrations were determined for up to 12 h in 6 horses following intravenous and oral phenylbutazone administration. To evaluate the bioavailability of different oral preparations, phenylbutazone was administered in a paste as well as the traditional powder form. The effect of the state of stomach contents on the absorption of phenylbutazone was investigated by administering the paste before and after feeding; the powder was given in a small bran mash and a full feed of lucerne chaff, wheaten chaff and bran. Despite great variability among individual horses both the pa...
Glucose utilization in the horse.
The British journal of nutrition    July 1, 1982   Volume 48, Issue 1 111-117 doi: 10.1079/bjn19820093
Ford EJ, Evans J.1. Total entry, irreversible loss and recycling rates of glucose were measured in four non-pregnant female Shetland ponies before and after a 24 h fast by the continuous intravenous infusion of a mixture of [U-14C]glucose and [2-3H]glucose. 2. The post-fasting fall in the concentration of glucose and the rise in the concentration of ketones in plasma were not significant. 3. After fasting the total entry rate fell from 1.44 +/- 0.11 (n4) to 1.19 +/- 0.12 mg/min per kg body-weight (P less than 0.01) and irreversible loss fell from 1.36 +/- 0.10 (n4) to 1.05 +/- 0.10 mg/min per kg body-weight (P...
Hemodynamic effects of prostacyclin (prostaglandin I2) in conscious ponies.
American journal of veterinary research    July 1, 1982   Volume 43, Issue 7 1128-1131 
Moore JN, Garner HE, Shapland JE, Roberts MC.The infusion (IV) of prostacyclin (PGI2) into conscious ponies resulted in systemic arterial hypotension and tachycardia. Mean systemic arterial pressure decreased from 103.3 mm of Hg to 88.5 mm of Hg when 125 ng of PGI2/kg/minute was infused, and heart rate increased from 55.0 to 102.0 beats/minute. When 208 ng of PGI2/kg/minute was infused, mean systemic arterial pressure decreased from 103.3 to 78.0 mm of Hg and heart rate increased from 55.0 to 109.3 beats/minute. There were no significant alterations in pulmonary arterial pressure, lactate, PCV, total WBC count, platelet count, serum lact...
[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