Efficacy and safety of enoxaparin during hemodialysis: Results from the HENOX study

Background: Low molecular weight heparins (LMWHs) have been suggested as an anticoagulant in hemodialysis (HD) since they provide convenient usage, safety and effective outcomes. Objective: Determine clinical efficacy and safety of enoxaparin sodium for the anticoagulation effect during HD in 99 cli...

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Main Authors: Vareesangthip K., Thitiarchakul S., Kanjanakul I., Sumethkul V., Krairittichai U., Chittinandana A., Bannachak D.
Format: Article
Language:English
Published: 2014
Online Access:http://www.scopus.com/inward/record.url?eid=2-s2.0-79251592841&partnerID=40&md5=d420f4eef9deedaf71a847053a008bab
http://cmuir.cmu.ac.th/handle/6653943832/3799
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Institution: Chiang Mai University
Language: English
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spelling th-cmuir.6653943832-37992014-08-30T02:35:20Z Efficacy and safety of enoxaparin during hemodialysis: Results from the HENOX study Vareesangthip K. Thitiarchakul S. Kanjanakul I. Sumethkul V. Krairittichai U. Chittinandana A. Bannachak D. Background: Low molecular weight heparins (LMWHs) have been suggested as an anticoagulant in hemodialysis (HD) since they provide convenient usage, safety and effective outcomes. Objective: Determine clinical efficacy and safety of enoxaparin sodium for the anticoagulation effect during HD in 99 clinically stable end-stage renal disease (ESRD) patients. Material and Method: This prospective open-label study was conducted in seven hemodialysis centers in Thailand. HD prescription during the present study was similar to the previous prescriptions including the type of dialyzer. Enoxaparin sodium 0.7 mg/kg was administered into a pre-dialyzer arterial line at the beginning of the HD session. The anticoagulation effect was monitored by visual inspection of the HD line hourly and inspection of the dialyzer at the end of HD session. Vascular access compression time was monitored at both arterial and venous sites separately at the end of the HD. Results: HD with enoxaparin sodium resulted in no fibrin/clot formation in a hemodialysis line in 97 cases (98%), and no significant clot formation in a dialyzer in 96 cases (97%). The mean vascular compression time was 5.63 ± 1.90 minutes at the arterial site and 5.72 ± 2.61 minutes at the venous site. Neither major adverse events nor major hemorrhages were reported. Prolonged activated partial thromboplastin times (aPTT) at 30 minutes after hemodialysis were reported in two cases. These abnormal aPTT cases returned to normal levels within 24 hours and 72 hours, respectively. Conclusion: The present study suggests that a single-dose regimen of enoxaparin sodium 0.7 mg/kg is an effective, well-tolerated, and convenient alternative to sodium heparin. 2014-08-30T02:35:20Z 2014-08-30T02:35:20Z 2011 Article 1252208 21425724 JMTHB http://www.scopus.com/inward/record.url?eid=2-s2.0-79251592841&partnerID=40&md5=d420f4eef9deedaf71a847053a008bab http://cmuir.cmu.ac.th/handle/6653943832/3799 English
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
language English
description Background: Low molecular weight heparins (LMWHs) have been suggested as an anticoagulant in hemodialysis (HD) since they provide convenient usage, safety and effective outcomes. Objective: Determine clinical efficacy and safety of enoxaparin sodium for the anticoagulation effect during HD in 99 clinically stable end-stage renal disease (ESRD) patients. Material and Method: This prospective open-label study was conducted in seven hemodialysis centers in Thailand. HD prescription during the present study was similar to the previous prescriptions including the type of dialyzer. Enoxaparin sodium 0.7 mg/kg was administered into a pre-dialyzer arterial line at the beginning of the HD session. The anticoagulation effect was monitored by visual inspection of the HD line hourly and inspection of the dialyzer at the end of HD session. Vascular access compression time was monitored at both arterial and venous sites separately at the end of the HD. Results: HD with enoxaparin sodium resulted in no fibrin/clot formation in a hemodialysis line in 97 cases (98%), and no significant clot formation in a dialyzer in 96 cases (97%). The mean vascular compression time was 5.63 ± 1.90 minutes at the arterial site and 5.72 ± 2.61 minutes at the venous site. Neither major adverse events nor major hemorrhages were reported. Prolonged activated partial thromboplastin times (aPTT) at 30 minutes after hemodialysis were reported in two cases. These abnormal aPTT cases returned to normal levels within 24 hours and 72 hours, respectively. Conclusion: The present study suggests that a single-dose regimen of enoxaparin sodium 0.7 mg/kg is an effective, well-tolerated, and convenient alternative to sodium heparin.
format Article
author Vareesangthip K.
Thitiarchakul S.
Kanjanakul I.
Sumethkul V.
Krairittichai U.
Chittinandana A.
Bannachak D.
spellingShingle Vareesangthip K.
Thitiarchakul S.
Kanjanakul I.
Sumethkul V.
Krairittichai U.
Chittinandana A.
Bannachak D.
Efficacy and safety of enoxaparin during hemodialysis: Results from the HENOX study
author_facet Vareesangthip K.
Thitiarchakul S.
Kanjanakul I.
Sumethkul V.
Krairittichai U.
Chittinandana A.
Bannachak D.
author_sort Vareesangthip K.
title Efficacy and safety of enoxaparin during hemodialysis: Results from the HENOX study
title_short Efficacy and safety of enoxaparin during hemodialysis: Results from the HENOX study
title_full Efficacy and safety of enoxaparin during hemodialysis: Results from the HENOX study
title_fullStr Efficacy and safety of enoxaparin during hemodialysis: Results from the HENOX study
title_full_unstemmed Efficacy and safety of enoxaparin during hemodialysis: Results from the HENOX study
title_sort efficacy and safety of enoxaparin during hemodialysis: results from the henox study
publishDate 2014
url http://www.scopus.com/inward/record.url?eid=2-s2.0-79251592841&partnerID=40&md5=d420f4eef9deedaf71a847053a008bab
http://cmuir.cmu.ac.th/handle/6653943832/3799
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