Well Being of Obstetric Patients on Minimal Blood Transfusions (WOMB)

Sanquin Research & Blood Bank Divisions

Status and phase: Completed; Phase 4

Conditions: Anemia

Treatments: Other: Red blood cell transfusion

Study type: Interventional

Funder types: Other

Identifiers

NCT00335023

01-021b

NTR335 (Registry Identifier)

0904 (Other Grant/Funding Number)

Details and patient eligibility

About

Postpartum haemorrhage (PPH) is one of the top five causes of maternal mortality in developed and developing countries. The most important treatment of PPH is red blood cell (RBC) transfusion. The decision whether to prescribe RBC transfusion is mostly based on postpartum haemoglobin (Hb) values. RBC transfusion should be aimed to reduce morbidity and especially to improve Health Related Quality of Life (HRQoL). The goal of the WOMB study is to assess the effect of RBC transfusion on HRQoL and to confirm the role of HRQoL in deciding whether RBC transfusion is necessary.

Full description

The WOMB study is a multicenter trial in patients with PPH, where a restrictive RBC transfusion policy will be compared with a more liberal RBC transfusion policy. Primary outcome in this study is fatigue measured with the MFI questionnaire. Inclusion criteria are: 1) 12-24 h after VD or CS; 2) 4.8 ≤Hb≤ 7.9 g/dL; 3) blood loss ≥ 1000mL or Hb decrease ≥ 1,9 g/dL; 4) age≥ 18 years; 5) no anaemic symptoms. Patients will be randomised for a RBC transfusion or not. The total follow-up period is 6 weeks. HRQoL will be measured at T=0 (12-24 hours postpartum) 3 days, 1, 3 and 6 weeks postpartum. At T=0 and 6 weeks postpartum Hb value will be measured. For the patients who receive a RBC transfusion, the effect of the RBC transfusion will be measured with the Hb value, Hct, platelet and leukocyte count, and the temperature of the patient before and after the RBC transfusion. The sample size is 500 patients: 250 allocated to a RBC transfusion and 250 patients allocated to a restrictive policy.

Enrollment: 500 patients

Sex: Female

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Women older than 18 years
• 12-24 hours after delivery (vaginal or caesarean section)
• Patients are in a clinical obstetric setting
• Blood loss of more than 1000 mL or Hb decrease ≥ 1,9 g/dL
• Hb value between 4.8 g/dL and 7.9 g/dL
• Working knowledge of the national language
• Written consent for participating this study (informed consent)

Exclusion criteria

• Patients with severe preeclampsia/ HELLP syndrome
• RBC transfusion during or after delivery but before t=0
• Patients with malignancy
• Patients with severe congenital haemolytic disease, like thalassemia or sickle cell disease
• Patients with compromised immunological status, congenital or acquired by medical treatment or infectious disease (eg. HIV)
• Severe active infectious disease at the time of proposed inclusion
• Severe cardiac, pulmonary, neurological, metabolic or psychiatric co- morbidity (ASA II/III) at the time of proposed inclusion
• Severe physical complaints (tachycardia of more than 100 bpm, dyspnoea, syncope, heart problems) at the time of intended inclusion
• Peripartum death of the newborn, or the newborn being in critical condition on neonatal intensive care

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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500 participants in 2 patient groups

Red blood cell transfusion

Active Comparator group

Description:

At least one unit of red blood cells will be administered.

Treatment:

Other: Red blood cell transfusion

Control

No Intervention group

Description:

No red blood cell transfusion. Iron suppletion is allowed and can be administered according to local protocol. If suppletion is prescribed, the type and duration will be registered