SMaRT Blood: Single-unit Versus Multiple-unit Packed Red Blood Cell Transfusion in Non-acute Postpartum Anemia (SMaRTBlood)
Primary Purpose
Postpartum Anemia Nos
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Blood Transfusion
Sponsored by

About this trial
This is an interventional treatment trial for Postpartum Anemia Nos
Eligibility Criteria
Inclusion Criteria:
- Women over 18
- Willing and stable to give consent
- > 6 hours postpartum from any mode of delivery
Determined by their physician to require blood transfusion either by:
- Hb <7g/dL OR
- >7g/dL with any sign or symptom of anemia such as fatigue, dizziness, tachycardia, or hypotension
- Agreed to accept blood transfusion
- No contraindications to blood transfusion
Exclusion Criteria:
- hemoglobinopathies
- patients with an ejection fraction <35%
- Hb <5 g/dL
- HR > 130 bpm, BP < 80/40
Sites / Locations
- Hospital of the University of Pennsylvania
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Single-Unit Blood Transfusion Protocol
Multiple-Unit Blood Transfusion Protocol
Arm Description
In this arm, patients receive a 1 unit pRBC transfusion with the plan for post-transfusion blood count at 4-6 hours post-transfusion and clinical reassessment.
In this arm, patients receive 2 units of pRBCs, followed by 4-6 hour post-transfusion blood count and clinical reassessment.
Outcomes
Primary Outcome Measures
Total Number of Units Transfused
To determine if there is a difference between single-unit and multiple-unit transfusion protocols in total number of units transfused
Secondary Outcome Measures
Length of Stay
To determine if there is a difference between single-unit and multiple-unit transfusion protocols in length of stay in days
Number of Participants Exclusively Breastfeeding at 4-9 Weeks Postpartum
To determine if there is a difference between single-unit and multiple-unit transfusion protocols in exclusive breastfeeding rates at 4-9 weeks postpartum.
Rate of Depression
• To determine if there is a difference between single-unit and multiple-unit transfusion protocols in Edinburgh Postnatal Depression Scale score at 4-9 weeks postpartum. EPDS scores range from 0-30, with higher scores (particularly above 10) are indicative of depression.
Rate of Fatigue
• To determine if there is a difference between single-unit and multiple-unit transfusion protocols in Multidimensional Fatigue Inventory scores at 4-9 weeks postpartum. This score ranges from 0-140 with higher scores indicating worse fatigue.
Maternal Attachment Inventory Scores
• To determine if there is a difference between single-unit and multiple-unit transfusion protocols in Maternal Attachment Inventory scores at 4-9 weeks postpartum. The possible range of scores is 26-104. Higher scores indicate higher maternal attachment to the infant.
Infection Rate
Development of any deep or superficial infection
Full Information
NCT ID
NCT03419780
First Posted
January 17, 2018
Last Updated
November 3, 2020
Sponsor
University of Pennsylvania
1. Study Identification
Unique Protocol Identification Number
NCT03419780
Brief Title
SMaRT Blood: Single-unit Versus Multiple-unit Packed Red Blood Cell Transfusion in Non-acute Postpartum Anemia
Acronym
SMaRTBlood
Official Title
Can a Single-unit Blood Transfusion Protocol in Obstetrics Reduce Total Number of Units Transfused? A Randomized, Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
November 2020
Overall Recruitment Status
Completed
Study Start Date
March 1, 2018 (Actual)
Primary Completion Date
June 1, 2020 (Actual)
Study Completion Date
June 1, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Pennsylvania
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
There is a paucity of data on management of non-acute postpartum anemia. Although blood transfusions were historically initiated with 2 units, the most recent recommendation from the American Association of Blood Banks is to begin with 1 unit. As no randomized controlled trials have been performed in obstetrics, the investigators propose a randomized, controlled trial in non-acute postpartum anemia comparing single- versus multiple-unit transfusion by total numbers of units transfused and maternal morbidity.
Detailed Description
Postpartum hemorrhage (PPH), which accounts for 30% of all direct maternal deaths, is the single most important cause of maternal morbidity and mortality across the globe and is a focus of attention of national organizations such as the Council for Patient Safety in Women's Health in recent years. Yet, there remains a paucity of data on the appropriate management of non-acute postpartum anemia.
It is common practice in obstetrics to offer a transfusion of packed red blood cells (pRBCs) to women with a hemoglobin (Hb) value less than 7 g/dL (hematocrit less than 20%) and to symptomatic women with even higher hemoglobin levels. Although transfusions were historically initiated with 2 units of pRBCs, the most recent recommendation from the American Association of Blood Banks (AABB) for a stable patient is to begin with 1 unit and reassess. However, while surgical data has successfully demonstrated that liberal blood transfusion increases morbidity and mortality in comparison to restricted transfusion, no randomized controlled trials have been performed in obstetrics to demonstrate superiority of a single-unit transfusion protocol.
The investigators propose a randomized, controlled trial in non-acute postpartum anemia comparing single-unit versus multiple-unit transfusion by total numbers of units transfused and maternal morbidity at the University of Pennsylvania with the hypothesis that single-unit transfusions can reduce the number of units transfused without increasing maternal morbidity.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Postpartum Anemia Nos
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
66 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Single-Unit Blood Transfusion Protocol
Arm Type
Active Comparator
Arm Description
In this arm, patients receive a 1 unit pRBC transfusion with the plan for post-transfusion blood count at 4-6 hours post-transfusion and clinical reassessment.
Arm Title
Multiple-Unit Blood Transfusion Protocol
Arm Type
Active Comparator
Arm Description
In this arm, patients receive 2 units of pRBCs, followed by 4-6 hour post-transfusion blood count and clinical reassessment.
Intervention Type
Biological
Intervention Name(s)
Blood Transfusion
Intervention Description
Patients are randomized to receive 1 or 2 units of packed red blood cells for initial transfusion.
Primary Outcome Measure Information:
Title
Total Number of Units Transfused
Description
To determine if there is a difference between single-unit and multiple-unit transfusion protocols in total number of units transfused
Time Frame
From randomization until discharge from admission for delivery, an average of 2-3 days
Secondary Outcome Measure Information:
Title
Length of Stay
Description
To determine if there is a difference between single-unit and multiple-unit transfusion protocols in length of stay in days
Time Frame
From randomization until discharge from admission for delivery, an average of 2-3 days
Title
Number of Participants Exclusively Breastfeeding at 4-9 Weeks Postpartum
Description
To determine if there is a difference between single-unit and multiple-unit transfusion protocols in exclusive breastfeeding rates at 4-9 weeks postpartum.
Time Frame
At 4-9 weeks after randomization
Title
Rate of Depression
Description
• To determine if there is a difference between single-unit and multiple-unit transfusion protocols in Edinburgh Postnatal Depression Scale score at 4-9 weeks postpartum. EPDS scores range from 0-30, with higher scores (particularly above 10) are indicative of depression.
Time Frame
4-9 weeks after randomization
Title
Rate of Fatigue
Description
• To determine if there is a difference between single-unit and multiple-unit transfusion protocols in Multidimensional Fatigue Inventory scores at 4-9 weeks postpartum. This score ranges from 0-140 with higher scores indicating worse fatigue.
Time Frame
4-9 weeks after randomization
Title
Maternal Attachment Inventory Scores
Description
• To determine if there is a difference between single-unit and multiple-unit transfusion protocols in Maternal Attachment Inventory scores at 4-9 weeks postpartum. The possible range of scores is 26-104. Higher scores indicate higher maternal attachment to the infant.
Time Frame
4-9 weeks after randomization
Title
Infection Rate
Description
Development of any deep or superficial infection
Time Frame
From randomization until 4-9 week postpartum visit
10. Eligibility
Sex
Female
Gender Based
Yes
Gender Eligibility Description
Eligibility is determined by delivery of a fetus.
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Women over 18
Willing and stable to give consent
> 6 hours postpartum from any mode of delivery
Determined by their physician to require blood transfusion either by:
Hb <7g/dL OR
>7g/dL with any sign or symptom of anemia such as fatigue, dizziness, tachycardia, or hypotension
Agreed to accept blood transfusion
No contraindications to blood transfusion
Exclusion Criteria:
hemoglobinopathies
patients with an ejection fraction <35%
Hb <5 g/dL
HR > 130 bpm, BP < 80/40
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sindhu K Srinivas, MD MSCE
Organizational Affiliation
University of Pennsylvania
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital of the University of Pennsylvania
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
34932836
Citation
Carson JL, Stanworth SJ, Dennis JA, Trivella M, Roubinian N, Fergusson DA, Triulzi D, Doree C, Hebert PC. Transfusion thresholds for guiding red blood cell transfusion. Cochrane Database Syst Rev. 2021 Dec 21;12(12):CD002042. doi: 10.1002/14651858.CD002042.pub5.
Results Reference
derived
PubMed Identifier
32652065
Citation
Hamm RF, Perelman S, Wang EY, Levine LD, Srinivas SK. Single-unit vs multiple-unit transfusion in hemodynamically stable postpartum anemia: a pragmatic randomized controlled trial. Am J Obstet Gynecol. 2021 Jan;224(1):84.e1-84.e7. doi: 10.1016/j.ajog.2020.07.007. Epub 2020 Jul 9.
Results Reference
derived
Learn more about this trial
SMaRT Blood: Single-unit Versus Multiple-unit Packed Red Blood Cell Transfusion in Non-acute Postpartum Anemia
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