Desmopressin acetate use in von Willebrand’s disease: a survey on current practices in Brazil
Introduction: von Willebrand’s disease (VWD) is the most common inherited bleeding disorder. The 1-desamino-8-d-arginine vasopressin (DDAVP) is the treatment of choice for most responsive patients with VWD. The aim of this study was to evaluate DDAVP use in the management of VWD. Method: We implemen...
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doaj-0dced98f40f84be4a162a7380fc7f4382021-02-25T04:19:47ZengElsevierHematology, Transfusion and Cell Therapy2531-13792021-01-014314349Desmopressin acetate use in von Willebrand’s disease: a survey on current practices in BrazilMaria Sueli da Silva Namen Lopes0Suely Meireles Rezende1Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, MG, BrazilCorresponding author at: Department of Internal Medicine, Faculty of Medicine, Universidade Federal de Minas Gerais, Av Alfredo Balena, 190, Belo Horizonte, MG, CEP 30130-110, Brazil.; Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, MG, BrazilIntroduction: von Willebrand’s disease (VWD) is the most common inherited bleeding disorder. The 1-desamino-8-d-arginine vasopressin (DDAVP) is the treatment of choice for most responsive patients with VWD. The aim of this study was to evaluate DDAVP use in the management of VWD. Method: We implemented a survey targeting medical doctors involved in the management of VWD in Brazil. Data was collected during a national congress on Hematology in November 2017. Main results: A total of 51/80 (63.8%) questionnaires were collected. Most participants (76.2%) were hematologists who assisted adult patients and approximately 60% worked at hemophilia treatment centers (HTCs). Approximately half of participants who reported treating patients with VWD, assisted on average, less than 5 patients per month, and approximately 60% declared not having used any DDAVP for treating VWD in the previous year. However, most participants (70%) prescribed FVIII-containing VWF concentrate (VWF/FVIII) for 1–10 patients in the previous year. More than 80% of the participants recognized the main indications for DDAVP. Physicians who recognized indication for DDAVP for type 1 VWD more often had prescribed DDAVP in previous year (p = 0.03). Barriers for prescribing DDAVP varied and included unavailability of laboratory facilities and consumables for DDAVP testing and lack of skills on its prescription. Conclusion: The DDAVP is currently underused in Brazil, as opposed to the excessive use of VWF/FVIII in VWD patients. We suggest the adoption of measures targeting educational and auditing programs. Furthermore, availability of laboratory reagents is needed to evaluate response and increment the correct use of DDAVP.http://www.sciencedirect.com/science/article/pii/S2531137920300067DDAVPDesmopressin von Willebrand’s disease survey Brazil |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Maria Sueli da Silva Namen Lopes Suely Meireles Rezende |
spellingShingle |
Maria Sueli da Silva Namen Lopes Suely Meireles Rezende Desmopressin acetate use in von Willebrand’s disease: a survey on current practices in Brazil Hematology, Transfusion and Cell Therapy DDAVP Desmopressin von Willebrand’s disease survey Brazil |
author_facet |
Maria Sueli da Silva Namen Lopes Suely Meireles Rezende |
author_sort |
Maria Sueli da Silva Namen Lopes |
title |
Desmopressin acetate use in von Willebrand’s disease: a survey on current practices in Brazil |
title_short |
Desmopressin acetate use in von Willebrand’s disease: a survey on current practices in Brazil |
title_full |
Desmopressin acetate use in von Willebrand’s disease: a survey on current practices in Brazil |
title_fullStr |
Desmopressin acetate use in von Willebrand’s disease: a survey on current practices in Brazil |
title_full_unstemmed |
Desmopressin acetate use in von Willebrand’s disease: a survey on current practices in Brazil |
title_sort |
desmopressin acetate use in von willebrand’s disease: a survey on current practices in brazil |
publisher |
Elsevier |
series |
Hematology, Transfusion and Cell Therapy |
issn |
2531-1379 |
publishDate |
2021-01-01 |
description |
Introduction: von Willebrand’s disease (VWD) is the most common inherited bleeding disorder. The 1-desamino-8-d-arginine vasopressin (DDAVP) is the treatment of choice for most responsive patients with VWD. The aim of this study was to evaluate DDAVP use in the management of VWD. Method: We implemented a survey targeting medical doctors involved in the management of VWD in Brazil. Data was collected during a national congress on Hematology in November 2017. Main results: A total of 51/80 (63.8%) questionnaires were collected. Most participants (76.2%) were hematologists who assisted adult patients and approximately 60% worked at hemophilia treatment centers (HTCs). Approximately half of participants who reported treating patients with VWD, assisted on average, less than 5 patients per month, and approximately 60% declared not having used any DDAVP for treating VWD in the previous year. However, most participants (70%) prescribed FVIII-containing VWF concentrate (VWF/FVIII) for 1–10 patients in the previous year. More than 80% of the participants recognized the main indications for DDAVP. Physicians who recognized indication for DDAVP for type 1 VWD more often had prescribed DDAVP in previous year (p = 0.03). Barriers for prescribing DDAVP varied and included unavailability of laboratory facilities and consumables for DDAVP testing and lack of skills on its prescription. Conclusion: The DDAVP is currently underused in Brazil, as opposed to the excessive use of VWF/FVIII in VWD patients. We suggest the adoption of measures targeting educational and auditing programs. Furthermore, availability of laboratory reagents is needed to evaluate response and increment the correct use of DDAVP. |
topic |
DDAVP Desmopressin von Willebrand’s disease survey Brazil |
url |
http://www.sciencedirect.com/science/article/pii/S2531137920300067 |
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