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  4. Developing dual hemofiltration plus cardiopulmonary bypass in rodents
 
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Developing dual hemofiltration plus cardiopulmonary bypass in rodents

Journal
Journal of Surgical Research
Journal Volume
195
Journal Issue
1
Pages
196-203
Date Issued
2015
Author(s)
Shinozaki K.
Lampe J.W.
CHIH-HSIEN WANG  
Yin T.
Kim J.
Oda S.
Hirasawa H.
Becker L.B.
DOI
10.1016/j.jss.2014.12.004
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84964247780&doi=10.1016%2fj.jss.2014.12.004&partnerID=40&md5=4c6f8958dbf724318ae5d19b436fa6ee
https://scholars.lib.ntu.edu.tw/handle/123456789/560311
Abstract
Emerging therapies for prolonged cardiac arrest (CA) include advanced circulatory interventions like emergency cardiopulmonary bypass (ECPB) and continuous venovenous hemofiltration (CVVHF). However, preclinical studies are limited because of the absence of a practical method of using CVVHF along with ECPB in rodents. We modified a CA model with ECPB resuscitation to include the CVVHF circuit. Adult rats were cannulated via the femoral artery or vein and the jugular vein for the ECPB circuit. A new circuit for CVVHF was added to allow ECPB and CVVHF to be started simultaneously. CVVHF blood flow at 3 mL/min could be controlled with a screw clamp during ECPB. After cessation of ECPB, the CVVHF flow was maintained using a roller pump. The filtration rate was controlled at 40 mL/h/kg in the standard volume of CVVHF and 120 mL/h/kg in the high volume (HV) of CVVHF. The driving force of hemofiltration was evaluated by monitoring transmembrane pressure and filter clearance (FCL). Transmembrane pressure in both groups was stable for 6 h throughout CVVHF. FCL of blood urea nitrogen and potassium in the standard volume group was significantly less than the HV group (P < 0.01). FCL of blood urea nitrogen and potassium was stable throughout the CVVHF operation in both groups. We developed a method of CVVHF along with ECPB in rodents after CA. We further demonstrated the ability to regulate both standard and HV filtration rates.
SDGs

[SDGs]SDG3

Publisher
Academic Press Inc.
Type
journal article

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