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  3. Correction of haemostasis can be reduced to four days for CVAD implantation in severe haemophilia A patients: Data from the PedNet study group.

Correction of haemostasis can be reduced to four days for CVAD implantation in severe haemophilia A patients: Data from the PedNet study group.

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DOI
10.48350/154663
Publisher DOI
10.1111/hae.14231
PubMed ID
33745218
Abstract
INTRODUCTION

Central venous access devices (CVAD) are used to facilitate intravenous treatment with coagulation factor concentrates (CFCs) in haemophilia A (HA). Guidelines for perioperative CFC replacement therapy are based on single centre experiences, and the length of replacement therapy varies.

AIM

The aim of this study was to evaluate whether haemostasis coverage under four days is as effective and safe as a longer period of haemostatic coverage.

METHODS

We identified patients with severe HA without inhibitors or major bleeds within one month of the surgery who received their first CVAD. We compared the CFC consumption and bleeds between children with ≤4 and those who received 5-7 perioperative treatment days including the day of surgery. Bleeds were recorded up to 4 days after the end of perioperative haemostatic coverage.

RESULTS

In total, 144 children met the eligibility criteria and were included in the study cohort: 34 had received haemostatic coverage for ≤4 days, while 110 had received 5-7 days of haemostatic coverage. One bleed related to the surgery occurred in both groups.

CONCLUSION

Overall, the bleeding complications were rare. Haemostatic coverage with CFCs under ≤4 days with elective CVAD insertions was as effective as coverage for ≥5 days.
Date Issued
2021-05
Publication Type
Article
Subject(s)
600 Technology > 610 Medicine & health
Subjects
CVAD children haemophilia A replacement therapy surgery
Language(s)
en
Author(s)
Koskenvuo, Minna
Mäkipernaa, Anne
Nolan, Beatrice
Kobelt, Rainer Andreas  
Universitätsklinik für Kinderheilkunde  
Ranta, Susanna
Additional Credits
Universitätsklinik für Kinderheilkunde  
Journal
Haemophilia
Publisher
Wiley
ISSN
1365-2516
Access(Rights)
restricted
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