Gillian Davies, Samantha L Morello, Tatiana H Ferreira, Kyle J Bartholomew, Brett Nemke, Jason A Bleedorn
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Systemic blood samples and synovial fluid were collected prior to infusion and immediately prior to and 30 minutes after tourniquet removal. Tibial bone marrow aspirates were collected after tourniquet removal. Samples were analyzed for amikacin concentration.</p><p><strong>Results: </strong>Contrast IVRLP perfused the pelvic limb distal to the tourniquet with a median volume of 10 mL (range, 6 to 16 mL) and perfusion pressure of 77.5 mm Hg (range, 37 to 130 mm Hg). The median systemic amikacin concentration with the tourniquet in place was low (0.6 μg/mL) and increased to 11.5 μg/mL following removal. The amikacin concentrations in synovial fluid and bone marrow were 109.8 and 49.7 μg/mL, respectively, with high interdog variability.</p><p><strong>Conclusions: </strong>Contrast venography and tissue amikacin levels suggest that IVRLP is feasible in the canine pelvic limb as the amikacin concentrations in 75% of synovial fluid and 33% of bone marrow samples exceeded 10 times the MIC required to inhibit 90% of isolates (MIC90) reported for Staphylococcus pseudintermedius.</p><p><strong>Clinical relevance: </strong>This study offers a baseline protocol for canine IVRLP for use in limb infections. Further studies should focus on drug delivery optimization and clinical application.</p>","PeriodicalId":7754,"journal":{"name":"American journal of veterinary research","volume":" ","pages":"1-8"},"PeriodicalIF":1.3000,"publicationDate":"2025-05-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Feasibility of amikacin antimicrobial intravenous regional limb perfusion in canine pelvic limbs.\",\"authors\":\"Gillian Davies, Samantha L Morello, Tatiana H Ferreira, Kyle J Bartholomew, Brett Nemke, Jason A Bleedorn\",\"doi\":\"10.2460/ajvr.25.03.0098\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>To use contrast venography and intravascular pressure monitoring to determine optimal perfusion volumes during IV regional limb perfusion (IVRLP) and to determine systemic, articular, and osseous concentrations of amikacin achieved following IVRLP in dogs.</p><p><strong>Methods: </strong>Animals were anesthetized and had lateral saphenous vein catheters placed. Incremental IV contrast venography with pressure monitoring was performed on one limb with a tourniquet proximal to the stifle to estimate vascular filling volume. Intravenous regional limb perfusion was performed on the contralateral hindlimb using 5 mg/kg amikacin, IV, diluted to the total filling volume. Systemic blood samples and synovial fluid were collected prior to infusion and immediately prior to and 30 minutes after tourniquet removal. Tibial bone marrow aspirates were collected after tourniquet removal. Samples were analyzed for amikacin concentration.</p><p><strong>Results: </strong>Contrast IVRLP perfused the pelvic limb distal to the tourniquet with a median volume of 10 mL (range, 6 to 16 mL) and perfusion pressure of 77.5 mm Hg (range, 37 to 130 mm Hg). The median systemic amikacin concentration with the tourniquet in place was low (0.6 μg/mL) and increased to 11.5 μg/mL following removal. 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引用次数: 0
摘要
目的:利用静脉造影术和血管内压力监测来确定静脉局部肢体灌注(IVRLP)时的最佳灌注量,并确定IVRLP后狗体内阿米卡星的全身、关节和骨骼浓度。方法:动物麻醉后置外侧隐静脉导管。增加静脉造影术和压力监测,在一个肢体上使用止血带,以估计血管充盈量。对侧后肢静脉局部灌注阿米卡星5 mg/kg, IV,稀释至总填充体积。在输注前、取下止血带前和取下止血带后30分钟采集全身血液和滑液。取下止血带后采集胫骨骨髓。对样品进行阿米卡星浓度分析。结果:对比IVRLP对止血带远端骨盆肢体灌注,中位容积10 mL(范围6 ~ 16 mL),灌注压77.5 mm Hg(范围37 ~ 130 mm Hg)。止血带放置时,全身阿米卡星浓度中位数较低(0.6 μg/mL),取下止血带后升高至11.5 μg/mL。滑膜液和骨髓中阿米卡星浓度分别为109.8和49.7 μg/mL,狗间差异较大。结论:静脉造影和组织阿米卡星水平表明,IVRLP在犬盆腔肢体是可行的,因为75%的滑液和33%的骨髓样本中的阿米卡星浓度超过了抑制90%假中葡萄球菌分离物所需MIC (MIC90)的10倍。临床意义:本研究提供了犬IVRLP用于肢体感染的基线方案。进一步的研究应着眼于优化给药和临床应用。
Feasibility of amikacin antimicrobial intravenous regional limb perfusion in canine pelvic limbs.
Objective: To use contrast venography and intravascular pressure monitoring to determine optimal perfusion volumes during IV regional limb perfusion (IVRLP) and to determine systemic, articular, and osseous concentrations of amikacin achieved following IVRLP in dogs.
Methods: Animals were anesthetized and had lateral saphenous vein catheters placed. Incremental IV contrast venography with pressure monitoring was performed on one limb with a tourniquet proximal to the stifle to estimate vascular filling volume. Intravenous regional limb perfusion was performed on the contralateral hindlimb using 5 mg/kg amikacin, IV, diluted to the total filling volume. Systemic blood samples and synovial fluid were collected prior to infusion and immediately prior to and 30 minutes after tourniquet removal. Tibial bone marrow aspirates were collected after tourniquet removal. Samples were analyzed for amikacin concentration.
Results: Contrast IVRLP perfused the pelvic limb distal to the tourniquet with a median volume of 10 mL (range, 6 to 16 mL) and perfusion pressure of 77.5 mm Hg (range, 37 to 130 mm Hg). The median systemic amikacin concentration with the tourniquet in place was low (0.6 μg/mL) and increased to 11.5 μg/mL following removal. The amikacin concentrations in synovial fluid and bone marrow were 109.8 and 49.7 μg/mL, respectively, with high interdog variability.
Conclusions: Contrast venography and tissue amikacin levels suggest that IVRLP is feasible in the canine pelvic limb as the amikacin concentrations in 75% of synovial fluid and 33% of bone marrow samples exceeded 10 times the MIC required to inhibit 90% of isolates (MIC90) reported for Staphylococcus pseudintermedius.
Clinical relevance: This study offers a baseline protocol for canine IVRLP for use in limb infections. Further studies should focus on drug delivery optimization and clinical application.
期刊介绍:
The American Journal of Veterinary Research supports the collaborative exchange of information between researchers and clinicians by publishing novel research findings that bridge the gulf between basic research and clinical practice or that help to translate laboratory research and preclinical studies to the development of clinical trials and clinical practice. The journal welcomes submission of high-quality original studies and review articles in a wide range of scientific fields, including anatomy, anesthesiology, animal welfare, behavior, epidemiology, genetics, heredity, infectious disease, molecular biology, oncology, pharmacology, pathogenic mechanisms, physiology, surgery, theriogenology, toxicology, and vaccinology. Species of interest include production animals, companion animals, equids, exotic animals, birds, reptiles, and wild and marine animals. Reports of laboratory animal studies and studies involving the use of animals as experimental models of human diseases are considered only when the study results are of demonstrable benefit to the species used in the research or to another species of veterinary interest. Other fields of interest or animals species are not necessarily excluded from consideration, but such reports must focus on novel research findings. Submitted papers must make an original and substantial contribution to the veterinary medicine knowledge base; preliminary studies are not appropriate.