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1.
Vet Rec ; 174(17): 430, 2014 Apr 26.
Article in English | MEDLINE | ID: mdl-24603464

ABSTRACT

The efficacy and safety of a florfenicol plus flunixin meglumine formulation in the treatment of respiratory disease was evaluated in calves less than six weeks of age, compared with a positive control group treated with a well-established florfenicol formulation. A total of 210 calves, selected from nine sites in Belgium, France and Spain, showing severe signs of respiratory disease, were randomly assigned to treatment with either florfenicol plus flunixin meglumine (Resflor; MSD Animal Health) or florfenicol (Nuflor; MSD Animal Health), both administered subcutaneously once. Animals were clinically observed daily for 10 days following treatment initiation. The predominant respiratory pathogens were Pasteurella multocida, Mycoplasma bovis, Mannheimia haemolytica and Histophilus somni. All isolates were subject to in vitro sensitivity testing and found susceptible to florfenicol. In both groups, rectal temperature dropped and clinical index (depression and respiratory signs) significantly improved after treatment. Specifically, for the change in rectal temperature from pretreatment to six hours post-treatment, the florfenicol-flunixin formulation was found significantly superior to florfenicol. Moreover, the florfenicol-flunixin formulation alleviated the clinical signs of disease more rapidly, and was demonstrated to be non-inferior to florfenicol on days 4 and 10. The use of the product combining florfenicol and flunixin in calves is safe and efficacious in the treatment of outbreaks of bovine respiratory disease.


Subject(s)
Anti-Bacterial Agents/therapeutic use , Bovine Respiratory Disease Complex/drug therapy , Clonixin/analogs & derivatives , Disease Outbreaks/veterinary , Thiamphenicol/analogs & derivatives , Animals , Animals, Newborn , Anti-Bacterial Agents/adverse effects , Belgium/epidemiology , Body Temperature , Bovine Respiratory Disease Complex/microbiology , Cattle , Clonixin/adverse effects , Clonixin/therapeutic use , Disease Outbreaks/prevention & control , Drug Combinations , Female , Follow-Up Studies , France/epidemiology , Male , Microbial Sensitivity Tests/veterinary , Rectum/physiology , Severity of Illness Index , Spain/epidemiology , Thiamphenicol/adverse effects , Thiamphenicol/therapeutic use , Time Factors , Treatment Outcome
2.
Eur J Obstet Gynecol Reprod Biol ; 97(1): 65-70, 2001 Jul.
Article in English | MEDLINE | ID: mdl-11435012

ABSTRACT

OBJECTIVES: Comparative study of plasma progesterone and betaHCG kinetics following surgical treatment of ectopic pregnancy. STUDY DESIGN: Prospective study involving 62 patients with tubal ectopic pregnancies. Study of the kinetics of plasma progesterone and betaHCG, and the correlation coefficient between plasma progesterone and betaHCG levels during post-operative follow-up. RESULTS: Thirty-nine patients were treated by salpingostomy and 23 by salpingectomy. Analyzing the betaHCG kinetics according to treatment revealed that both curves were convergent on day 2. Progesterone kinetics differed greatly in that they appeared "parallel and confused". Analyzing the correlation between betaHCG and progesterone levels proved the absence of a significant link. CONCLUSIONS: Studying the kinetics of plasma progesterone after surgical treatment of ectopic pregnancies revealed a fast decrease in progesterone. Statistical analysis of the progesterone concentration showed that post-operative kinetics is fully independent from that of betaHCG. Progesterone therefore cannot be substituted to betaHCG for post-operative follow-up.


Subject(s)
Pregnancy, Tubal/blood , Pregnancy, Tubal/surgery , Progesterone/blood , Chorionic Gonadotropin, beta Subunit, Human/blood , Fallopian Tubes/surgery , Female , Humans , Kinetics , Pregnancy , Prospective Studies , Sensitivity and Specificity , Treatment Failure
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