Canada Spends Logo

Explorez notre analyse du budget 2026

Grant: Project Grant

University of Calgary

$742,052.00

A prospective cohort study evaluating peripartum anticoagulation management among pregnant women with VTE and its impact on patient outcomes

EF 2020-21

Résumé
Pregnant women are on daily injectable blood thinners if they are at risk of a blood clot in their legs (deep vein thrombosis) or lungs (pulmonary embolism) during pregnancy. This includes patients who have already had a blood clot, or those at risk of blood clots. While being on blood thinners helps to prevent blood clots, it can lead to complications at the time of labor and delivery. Being on blood thinners may increase the chance of heavier bleeding at the time of delivery, and may limit the ability to get an epidural anesthesia for pain control. Being off of blood thinners may increase the chance of getting a blood clot. Around the world, physicians recommend different strategies for what to do with the blood thinners around labor and delivery, and we do not know what the best strategy is. We will we follow pregnant women on injectable blood thinners at 13 hospitals around the world, to see what happens with their blood thinners at the time of labor and delivery, and the postpartum period. We will get blood work to measure a blood count and blood thinner level on the day of delivery, and a blood count 24 hours after delivery. We will collect information about the amount of blood lost at the time of delivery and other delivery details. We will see or call participants at 6 weeks and 90 days postpartum to assess for complications of bleeding, blood clots, and wound complications. Because the patient experience is very important, we will also ask participants about the choices they made and satisfaction with their delivery experience. We will also collect information about hospital resources used with each of the different management strategies. By better understanding what practices are happening around the world and collecting outcome information in a similar way at all participating centres, we can provide doctors and patients with more information about the risks and benefits of the different options of blood thinner management around delivery.
Programme
Project Grant
Bénéficiaire
Emplacement
Alberta, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
434526
Name
Skeith Leslie
Region
Alberta
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Human Development, Child and Youth Health
Theme2
Clinical
Prcname2
Clinical Investigation - A: Reproduction, Maternal, Child and Youth Health 2
Projecttitle
A prospective cohort study evaluating peripartum anticoagulation management among pregnant women with VTE and its impact on patient outcomes
Programtype2
Operating Grants
Orgnameinp2
University of Calgary
Cihramount2
$742,052
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Anticoagulation Management; Labor And Delivery; Patient Satisfaction; Postpartum Hemorrhage; Postpartum Period; Venous Thromboembolism
Abstract
Pregnant women are on daily injectable blood thinners if they are at risk of a blood clot in their legs (deep vein thrombosis) or lungs (pulmonary embolism) during pregnancy. This includes patients who have already had a blood clot, or those at risk of blood clots. While being on blood thinners helps to prevent blood clots, it can lead to complications at the time of labor and delivery. Being on blood thinners may increase the chance of heavier bleeding at the time of delivery, and may limit the ability to get an epidural anesthesia for pain control. Being off of blood thinners may increase the chance of getting a blood clot. Around the world, physicians recommend different strategies for what to do with the blood thinners around labor and delivery, and we do not know what the best strategy is. We will we follow pregnant women on injectable blood thinners at 13 hospitals around the world, to see what happens with their blood thinners at the time of labor and delivery, and the postpartum period. We will get blood work to measure a blood count and blood thinner level on the day of delivery, and a blood count 24 hours after delivery. We will collect information about the amount of blood lost at the time of delivery and other delivery details. We will see or call participants at 6 weeks and 90 days postpartum to assess for complications of bleeding, blood clots, and wound complications. Because the patient experience is very important, we will also ask participants about the choices they made and satisfaction with their delivery experience. We will also collect information about hospital resources used with each of the different management strategies. By better understanding what practices are happening around the world and collecting outcome information in a similar way at all participating centres, we can provide doctors and patients with more information about the risks and benefits of the different options of blood thinner management around delivery.
Competitiondate
202010
Approvedterm2
4 yrs 0 mth
Pinamesdelim
Skeith, Leslie; Malhamé, Isabelle; Malinowski, Ann K
Approvedterm
4 ans 0 mois
Cihrcontribution2
~ $742,052~ $0~