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Trials / Completed

CompletedNCT03738995

Retrospective Survey of Obstetric Red Cell Transfusion in a Tertiary Women's Hospital

Status
Completed
Phase
Study type
Observational
Enrollment
760 (actual)
Sponsor
KK Women's and Children's Hospital · Other Government
Sex
Female
Age
17 Years – 50 Years
Healthy volunteers

Summary

The decision for red cell transfusion is usually made empirically by clinicians. We aim to perform a two-year retrospective audit of obstetric red cell transfusions at a tertairy women's hospital to evaluate the (1) incidence of obstetric red cell transfusion, (2) indications for transfusion and (3) haemoglobin triggers and targets of transfusion. Obstetric patients who were given red cell or whole blood transfusion during their pregnancy and who delivered a live or still birth between 1 Jan 2014 to 31 Dec 2015 are included in the analysis. Findings of this study would provide insights into transfusion practice and appropriateness of obstetric red cell transfusion at a tertiary obstetric hospital in Singapore.

Detailed description

Studies suggest an inter-hospital variation in transfusion rates, despite the availability of transfusion guidelines. As part of an initiative to implement patient blood management at our institution, we conducted this retrospective cohort study with the aims of defining the incidence of red cell transfusion among our multiethnic obstetric population and evaluating transfusion practice, with regard to indications and appropriateness. Ethics approval has been obtained from the institutional review board. Patients who fulfil study criteria would be identified from the hospital's delivery and blood bank registries. Further information would be extracted from the medical records and blood bank database. The delivery registry would also be accessed to obtain the total number of parturients who delivered for the study period. The following data would be collected and a pro-forma completed: * Demographic data: age, body mass index, gravidity, parity * Obstetric data: gestation age at pregnancy booking, occurrence of obstetric conditions associated with bleeding, mode of delivery, estimated blood loss at delivery and antenatal prescription of iron therapy * Transfusion data: indications for red cell transfusion, number of transfusion events, haemoglobin (Hb) levels at different time points of pregnancy, location of transfusion, adverse events associated with transfusion, activation of massive transfusion protocol For the purpose of the study, a "transfusion event" is defined as the time interval between prescription of red cells and complete administration to patient. If multiple units were prescribed, all units are considered part of the single event if the time of prescription between consecutive units does not exceed 72 hours. The incidence of transfusion would be defined as the percentage of patients ('cases') requiring red cell transfusion antenatally and up to 6 weeks postnatally among ALL patients who delivered a live or still birth in the period 2014-2015. Statistical analysis would be performed using SPSS for windows, version 19 (IBM, Armonk, NY). Data would be presented as mean (+/- SD), median (IQR) or count (%), as appropriate. Missing data would be excluded from the analysis.

Conditions

Interventions

TypeNameDescription
BIOLOGICALRed cell or whole blood transfusion during pregnancy and up to 6 weeks postpartumAdministration of red cell or whole blood transfusion to parturients during pregnancy and up to 6 weeks postpartum

Timeline

Start date
2016-08-01
Primary completion
2018-03-30
Completion
2018-03-30
First posted
2018-11-13
Last updated
2018-11-13

Source: ClinicalTrials.gov record NCT03738995. Inclusion in this directory is not an endorsement.