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2021-05-16Zeitschriftenartikel DOI: 10.25646/8660
A Pilot Randomised Clinical Trial Comparing a Short-Term Perioperative Prophylaxis Regimen to a Long-Term Standard Protocol in Equine Colic Surgery
dc.contributor.authorStöckle, Sabita Diana
dc.contributor.authorKannapin, Dania A.
dc.contributor.authorKauter, Anne M. L.
dc.contributor.authorLübke-Becker, Antina
dc.contributor.authorWalther, Birgit
dc.contributor.authorMerle, Roswitha
dc.contributor.authorGehlen, Heidrun
dc.date.accessioned2021-06-16T08:22:59Z
dc.date.available2021-06-16T08:22:59Z
dc.date.issued2021-05-16none
dc.identifier.other10.3390/antibiotics10050587
dc.identifier.urihttp://edoc.rki.de/176904/8380
dc.description.abstractFor surgical interventions classified as clean or clean-contaminated, including laparotomy, guidelines in human and veterinary medicine recommend a short-term perioperative antibiotic prophylaxis (PAP). In equine colic surgery, however, PAP commonly exceeds 24 h. Objectives: The aim of this study was to compare a single-shot to a 5-day lasting PAP considering surgical site infections (SSI) and other adverse effects probably associated with the particular antimicrobial regimen. Study design: The study was designed as a randomised non-inferiority pilot study including horses subjected to colic surgery while receiving one of two distinct PAP regimens. Methods:All horses (n= 67) included in the study received the standard physical examination before and after surgery. Colic surgery was performed according to the current standard of the clinic. Horses were randomly assigned to two groups, receiving either the “single-shot” or the “5-day lasting”antibiotic prophylaxis. The “single-shot” group (n= 30) received penicillin and gentamicin onlyonce before and, if needed, during surgery, whereas the “5-day lasting” group (n= 37) received antibiotics for five days. In addition to the standard laboratory examinations, serum amyloid A and fibrinogen were determined preoperatively and during five days after surgery. SSI, postoperative colitis and haemolytic anaemia were classified as postoperative complications potentially related toantibiotic use. Results: The outcome of this preliminary non-inferiority clinical trial showed that the occurrence of postoperative adverse events (i.e., SSI, postoperative colitis and haemolytic anaemia)lacked significant differences between the study groups. Main limitations: The main limitations of this study are the limited group sizes and our inability to blind the study. Conclusions: Single-shot PAP seems to be an alternative approach considering the 5-day lasting protocol commonly used in equine abdominal surgery. However, a proper hygiene management together with a close clinical and laboratory monitoring of the equine patient is indispensable.eng
dc.language.isoengnone
dc.publisherRobert Koch-Institut
dc.rights(CC BY 3.0 DE) Namensnennung 3.0 Deutschlandger
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/de/
dc.subjectColiceng
dc.subjectlaparotomyeng
dc.subjectperioperative antibioticseng
dc.subjectsurgical site infectioneng
dc.subjectcolitiseng
dc.subjecthaemolytic anaemiaeng
dc.subjecthorseeng
dc.subject.ddc610 Medizin und Gesundheitnone
dc.titleA Pilot Randomised Clinical Trial Comparing a Short-Term Perioperative Prophylaxis Regimen to a Long-Term Standard Protocol in Equine Colic Surgerynone
dc.typearticle
dc.identifier.urnurn:nbn:de:kobv:0257-176904/8380-2
dc.identifier.doihttp://dx.doi.org/10.25646/8660
dc.type.versionpublishedVersionnone
local.edoc.container-titleantibioticsnone
local.edoc.container-issn2079-6382none
local.edoc.pages14none
local.edoc.type-nameZeitschriftenartikel
local.edoc.container-typeperiodical
local.edoc.container-type-nameZeitschrift
local.edoc.container-urlhttps://www.mdpi.com/2079-6382/10/5/587none
local.edoc.container-publisher-nameMDPInone
local.edoc.container-volume10none
local.edoc.container-issue5none
local.edoc.container-periodicalpart-titleOptimization and Improvement of Veterinary Antimicrobial Treatment to Reduce Antimicrobial Resistancenone
local.edoc.rki-departmentZentrum für Biologische Gefahren und Spezielle Pathogenenone
dc.description.versionPeer Reviewednone

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