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Topic:Disease control

Disease control in horses encompasses the strategies and measures implemented to prevent, manage, and eradicate infectious and non-infectious diseases within equine populations. This field involves the study of pathogen transmission, host-pathogen interactions, and the development of effective vaccination and biosecurity protocols. Disease control also includes monitoring and surveillance of equine health to identify outbreaks and implement timely interventions. Key aspects of disease control in horses involve understanding the epidemiology of equine diseases, improving diagnostic techniques, and enhancing treatment options. This page compiles peer-reviewed research studies and scholarly articles that explore various methodologies, technologies, and practices aimed at controlling diseases in horses, with a focus on improving overall equine health and welfare.
[Evaluation of the effectiveness of the preparation Eqvalan in the control of Nematoda in horses].
Wiadomosci parazytologiczne    January 1, 1986   Volume 32, Issue 2 199-202 
Grzywiński L, Kluczniok P, Połozowski A.No abstract available
A retrospective study of the serology of brucellosis in horses.
The Veterinary record    December 14, 1985   Volume 117, Issue 24 638-639 doi: 10.1136/vr.117.24.638
MacMillan AP.No abstract available
Equine influenza vaccination requirement.
The Veterinary record    December 14, 1985   Volume 117, Issue 24 646 doi: 10.1136/vr.117.24.646-c
Keith NW.No abstract available
A retrospective study of equine infectious anemia based on the canadian control program.
The Canadian veterinary journal = La revue veterinaire canadienne    December 1, 1985   Volume 26, Issue 12 373-377 
Paquette B.Equine infectious anemia in Canada was reviewed for the period January 1976 to December 1981. The human and ecological factors prevailing in Canada are deemed instrumental with respect to the evolution of the disease. The natural spread of the disease on a large scale has not been influenced by the Federal program. Reactors with signs of the disease are important for it's propagation. The author underlines the necessity of cooperation with private practising veterinarians to control it.
[Serologic studies on the occurrence of the arteritis virus in the horse in West Germany].
DTW. Deutsche tierarztliche Wochenschrift    November 26, 1985   Volume 92, Issue 11-12 461-463 
Herbst W, Danner K.No abstract available
Ragwort poisoning in horses.
The Veterinary record    November 2, 1985   Volume 117, Issue 18 479 doi: 10.1136/vr.117.18.479
Leyland A.No abstract available
Reflections on the diagnostic approach to multicentric lymphosarcoma in an aged Arabian mare.
Equine veterinary journal    November 1, 1985   Volume 17, Issue 6 467-469 doi: 10.1111/j.2042-3306.1985.tb02559.x
Mackey VS, Wheat JD.No abstract available
Erysipelothrix rhusiopathiae vegetative endocarditis in a horse.
Australian veterinary journal    November 1, 1985   Volume 62, Issue 11 392 doi: 10.1111/j.1751-0813.1985.tb14224.x
McCormicK BS, Peet RL, Downes K.No abstract available
Equine subcutaneous zygomycosis in Costa Rica.
Mykosen    November 1, 1985   Volume 28, Issue 11 545-549 doi: 10.1111/j.1439-0507.1985.tb02084.x
Mendoza L, Alfaro AA.No abstract available
Retrograde transport and neuron biology in a clinical context.
Equine veterinary journal    November 1, 1985   Volume 17, Issue 6 415-416 doi: 10.1111/j.2042-3306.1985.tb02544.x
Blakemore WE.No abstract available
Efficacy of testing for illegal medication in horses.
Journal of the American Veterinary Medical Association    November 1, 1985   Volume 187, Issue 9 927-930 
Woods WE, Chay S, Houston T, Blake JW, Tobin T.The efficacy of testing for illegal drugs in race horses was surveyed by evaluating 27 questionnaires received from 28 racing jurisdictions polled. Large variations in the number of samples tested and drugs detected were reported. Some jurisdictions reported only illegal medications, whereas others also reported permitted medications. To facilitate comparison, stimulants, depressants, local anesthetics, narcotic analgesics, and tranquilizers were classified as hard drugs. Other drugs, which are legal in some jurisdictions, were classified as soft. To evaluate the efficacy of testing, positive ...
The incidence of Chorioptes bovis (Acarina: Psoroptidae) on the feet of horses, sheep, and goats in the Netherlands.
The veterinary quarterly    October 1, 1985   Volume 7, Issue 4 283-289 doi: 10.1080/01652176.1985.9694001
Cremers HJ.The feet of horses, sheep, and goats of different breeds and from many different localities were examined for Chorioptes bovis. In horses, mites were mainly found in the Belgian and Frisian breeds (40% and 62% infected, respectively). In sheep and goats, respectively 63% and 86% were infected. In horses as well as in sheep and goats, mange-lesions were rarely seen. A number of sheep and goats were examined for mites and lesions quantitatively. In sheep all mites were restricted to the region close to the accessory digits and the claws. In goats the average number of mites was higher than in sh...
Studies on the immunogenicity of Streptococcus equi vaccines in foals.
Canadian journal of comparative medicine : Revue canadienne de medecine comparee    October 1, 1985   Volume 49, Issue 4 351-356 
Srivastava SK, Barnum DA.The ability of either formalin-treated or heat-inactivated whole Streptococcus equi cell vaccines or partially purified M-protein of S. equi to give rise to protective antibody levels was studied in Standardbred foals by serological means. Two commercial preparations, i.e. a beta-propiolactone killed whole S. equi cell bacterin and a cell-free extract of S. equi cells were included in the study. The mean passive hemagglutination antibody titers (10 X log2) in sera of foals given either four doses of formalin-treated whole cell vaccine or an initial dose of formalin-treated followed by three do...
Studies on histoplasmosis farciminosii (epizootic lymphangitis) in Egypt. III. Application of a skin test (‘Histofarcin’) in the diagnosis of epizootic lymphangitis in horses.
Mykosen    September 1, 1985   Volume 28, Issue 9 457-461 
Soliman R, Saad MA, Refai M.No abstract available
[Prevalence of equine toxoplasmosis evaluated by the indirect immunofluorescence technic, Matto Grosso do Sul, Brazil].
Boletin de la Oficina Sanitaria Panamericana. Pan American Sanitary Bureau    August 1, 1985   Volume 99, Issue 2 158-162 
Larangeira NL, Ishizuka MM, Hyakutake S.No abstract available
Salmonella shed by horses with colic.
Journal of the American Veterinary Medical Association    August 1, 1985   Volume 187, Issue 3 256-257 
Palmer JE, Benson CE, Whitlock RH.Salmonella was isolated from 13 of 100 colicky horses admitted to a referral hospital. Seven horses were shedding the microorganism at or soon after hospital admission. A unique serotype was introduced into the hospital by a horse not shedding Salmonella at admission. It was concluded that 8 horses were infected before admission. Whether the remaining 5 horses were infected before or after admission could not be determined. Salmonella senftenberg was the most commonly isolated serotype from colicky horses and from horses with salmonellosis that were not colicky on hospital admission during the...
Infectious diarrhoea in foals.
Equine veterinary journal    July 1, 1985   Volume 17, Issue 4 262-264 doi: 10.1111/j.2042-3306.1985.tb02492.x
Harbour DA.No abstract available
Survival of contagious equine metritis organisms (CEMO) in different transport media as influenced by storage time, temperature and contaminating flora.
Zentralblatt fur Veterinarmedizin. Reihe B. Journal of veterinary medicine. Series B    July 1, 1985   Volume 32, Issue 6 454-459 doi: 10.1111/j.1439-0450.1985.tb01982.x
Engvall A.No abstract available
Prevalence of equine onchocerciasis in southeastern and midwestern United States.
Journal of the American Veterinary Medical Association    June 1, 1985   Volume 186, Issue 11 1202-1203 
Cummings E, James ER.Of 664 horses reported to have originated in southeastern and midwestern United States, 341 (51.4%) were positive for Onchocerca cervicalis cutaneous microfilariasis. The highest prevalence of 68.8% was recorded for horses from Virginia. Horses with the highest concentrations of microfilariae (as high as 19,770 microfilariae/mg in 1 horse) were from the Southeast (Georgia, Florida, Tennessee, and Alabama). For horses from South Carolina, the prevalence of infection was 57.1%; from the Midwest (Kentucky, Illinois, Ohio, and Indiana), 54.4%; from North Carolina, 45.5%; from Pennsylvania, 7.7%; a...
Integrated control of Strongylus vulgaris infection in horses using ivermectin.
Equine veterinary journal    May 1, 1985   Volume 17, Issue 3 191-195 doi: 10.1111/j.2042-3306.1985.tb02466.x
Dunsmore JD.An attempt was made to control or eliminate Strongylus vulgaris from a closed group of three horses at pasture near Perth, Western Australia, by dosing with ivermectin on four occasions during the time of year when it was believed that environmental conditions would eliminate all the non-parasitic stages of that species. At necropsy, five months after the last dose of anthelmintic and after continually grazing the same pastures, no S vulgaris or arterial lesions were found in those horses and S edentatus, Draschia megastoma and Habronema species were also almost completely eliminated.
Epidemiological approach to the control of horse strongyles.
Equine veterinary journal    May 1, 1985   Volume 17, Issue 3 202-207 doi: 10.1111/j.2042-3306.1985.tb02470.x
Herd RP, Willardson KL, Gabel AA.An investigation of the spring rise in strongyle egg output of grazing horses on two commercial horse farms in northern USA in 1981 and 1982 revealed two distinct spring and summer rises in faecal egg counts, with peaks in May and August/September. There was a marked rise in the concentration of infective larvae on pasture two to four weeks after the peaks in egg output, so that grazing horses were at serious risk from June onwards and pasture larval counts on one farm did not fall to low levels until June of the following year. The spring and summer rises in faecal egg counts appeared to be s...
Equine influenza reactions.
The Veterinary record    April 27, 1985   Volume 116, Issue 17 478 doi: 10.1136/vr.116.17.478
Eagles BW, Higgins AJ.No abstract available
Prevention and control of infection.
The Veterinary clinics of North America. Equine practice    April 1, 1985   Volume 1, Issue 1 41-50 doi: 10.1016/s0749-0739(17)30768-x
Koterba AM, Brewer B, Drummond WH.Foal septicemia is a major cause of neonatal morbidity and mortality. In order to improve success rates, earlier diagnosis and treatment are essential. This article stresses methods to prevent and treat infections in the compromised equine neonate.
An outbreak of equine influenza at a harness horse racetrack.
The Cornell veterinarian    April 1, 1985   Volume 75, Issue 2 277-288 
Kemen MJ, Frank RA, Babish JB.An outbreak of an influenza-like illness affected approximately 1/3 of the 1050 race horses stabled at a standardbred racetrack and resulted in a 3-day suspension of racing. A/Equi-2 influenza virus was isolated from 1 affected horse and 8 of 10 horses sampled seroconverted. Threshold protective levels of HI antibody against A/Equi-2 influenza virus were not demonstrated in unaffected horses. Resistance in unaffected horses was assumed to result from other factors following previous exposure. Few of the horses had been vaccinated against equine influenza. It was felt that an outbreak of this m...
Reappearance of Getah virus infection among horses in Japan.
Nihon juigaku zasshi. The Japanese journal of veterinary science    April 1, 1985   Volume 47, Issue 2 333-335 doi: 10.1292/jvms1939.47.333
Sentsui H, Kono Y.No abstract available
Serologic surveillance for vesicular stomatitis virus on Ossabaw Island, Georgia.
Journal of wildlife diseases    April 1, 1985   Volume 21, Issue 2 100-104 doi: 10.7589/0090-3558-21.2.100
Fletcher WO, Stallknecht DE, Jenney EW.Seventeen species of mammals and seven species of birds from Ossabaw Island, Georgia, were tested for vesicular stomatitis (VS) neutralizing antibodies. Seropositive results were restricted to mammals with six of 17 species testing seropositive for VS (New Jersey type) neutralizing antibodies. Seropositive species included: raccoons (Procyon lotor), white-tailed deer (Odocoileus virginianus), feral swine (Sus scrofa), cattle (Bos taurus), horses (Equus caballus), and donkeys (Equus asinus). All tests for VS (Indiana type) were negative.
Vaccination against equine influenza.
The Veterinary record    March 9, 1985   Volume 116, Issue 10 275 doi: 10.1136/vr.116.10.275-b
Clarke KW.No abstract available
Intradermal transmission of Potomac horse fever.
The Veterinary record    March 2, 1985   Volume 116, Issue 9 246-247 doi: 10.1136/vr.116.9.246
Perry BD, Rikihisa Y, Saunders GK.No abstract available
Internal parasites of the horse and their control.
Equine veterinary journal    March 1, 1985   Volume 17, Issue 2 79-82 doi: 10.1111/j.2042-3306.1985.tb02054.x
Duncan JL.No abstract available
[EHV1, to vaccinate or not?].
Tijdschrift voor diergeneeskunde    March 1, 1985   Volume 110, Issue 5 189-190 
Binkhorst GJ, van Oirschot JT, Breukink HJ.No abstract available
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