Health Condition 1: D500- Iron deficiency anemia secondary to blood loss (chronic)
Conditions
Interventions
None listed
Sponsors
PGIMER Chandigarh
Eligibility
Inclusion criteria
Inclusion criteria: All pregnant women receiving transfusion during pregnancy till 6 weeks postpartum at PGIMER Patients willing to participate in study
Exclusion criteria
Exclusion criteria: Pregnant women who have received transfusion outside PGIMER Not willing to participate in study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To assess the amount and ratio of blood components administered during massive transfusions To determine the rate and nature of adverse transfusion reactions during obstetric transfusions at PGIMER To assess the rate of safe transfusion practices being followed by healthcare staff involved in management of obstetric patients To create MSBOS ( Maximum Surgical Blood Ordering Schedule) for patients undergoing elective as well as emergency caesarean section vs vaginal delivery Timepoint: all women recruited will be followed up till 6 weeks of blood transfusion | — |
Secondary
| Measure | Time frame |
|---|---|
| To assess the amount and ratio of blood components administered during massive transfusions To determine the rate and nature of adverse transfusion reactions during obstetric transfusions at PGIMER To assess the rate of safe transfusion practices being followed by healthcare staff involved in management of obstetric patients To create MSBOS ( Maximum Surgical Blood Ordering Schedule) for patients undergoing elective as well as emergency caesarean section vs vaginal delivery Timepoint: 1 year | — |
Countries
India
Contacts
Public ContactDr Plaksha goel
pgimer chandigarh
Outcome results
None listed