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| ID | Type | Description | Link |
|---|---|---|---|
| 2021-A01199-32 | Registry Identifier | IDRCB |
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| Name | Class |
|---|---|
| Etablissement Français du Sang (Nouvelle Aquitaine) | UNKNOWN |
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Chronic histiocytic intervillositis (CHI) is associated with severe and recurrent obstetrical complications. A link between anti-HLA Antibodies (Ab) and CHI has recently been established. At the Etablissement Français du Sang (EFS), donors who have already given birth once and have high levels of anti-HLA are excluded from donating apheresis platelets and therapeutic plasma to prevent TRALI (Transfusion Related Acute Lung Injury). No studies have examined the obstetrical history of these donors. The question is: is there an association between anti-HLA levels and obstetrical complications?
Chronic histiocytic intervillositis (CHI) is a rare condition with an incidence of around 5 in 10,000 pregnancies. It is defined by major infiltration of the intervillous cavity by CD68+ maternal histiocytes, associated with fibrin deposition on the villous surface.
CHI is associated with severe obstetrical complications and a very high recurrence rate, estimated at between 70% and 100%. These complications include early and late miscarriage, fetal death, severe growth retardation in surviving fetuses, and premature delivery. The survival rate reported in the literature varies between 30% and 50%.
Anti-HLA antibodies are present in 54% of pregnant women at the end of pregnancy, and their rate increases towards the end of pregnancy. The presence of HLA antibodies also increases with the number of pregnancies, and is found in up to 74% of cases after more than 2 deliveries.
The research question concerns the existence of a statistically significant association between the presence of high levels of anti-HLA antibodies and the occurrence of one or more obstetric complications.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Blood donors tested for anti-HLA Antibody | Blood donors tested for anti-HLA Antibody between 2010 and 2020 as part of TRALI prevention program. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Obstetrical history | Other | Selection of donors by EFS retrospectively on the basis of inclusion criteria. Information note sent by e-mail, non-opposition as well as a questionnaire to be completed online to obtain data on obstetrical history. |
| Measure | Description | Time Frame |
|---|---|---|
| To measure the association between the occurrence of obstetrical complications and the level of anti-HLA Ab measured during the screening test performed by the EFS. | Obstetrical complications are defined as (binomial qualitative variable) :
| 2 months |
| Measure | Description | Time Frame |
|---|---|---|
| Type and precocity of obstetrical complication (multinomial qualitative variable) |
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Inclusion Criteria:
Exclusion Criteria:
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Blood donors who were screened for anti-HLA Ab between 2010 and 2020 as part of TRALI prevention at the EFS Poitiers site histocompatibility laboratory.
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Xavier LAFARGE, Doctor | Contact | 05 56 90 83 93 | xavier.lafarge@efs.sante.fr | |
| Isabelle JOLLET | Contact | 05 49 61 57 27 | isabelle.jollet@efs.sante.fr |
| Name | Affiliation | Role |
|---|---|---|
| Xavier LAFARGE, Doctor | Etablissement Français du Sang (Nouvelle Aquitaine) | Principal Investigator |
| Alexandra BENACHI, Professor | APHP, Antoine Béclère Hospital, CLAMART, France | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Etablissement Français du Sang Nouvelle Aquitaine | Recruiting | Bordeaux | 33075 | France |
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| Anti-HLA Antibody tests | Other | Analyze responses in relation to the results of the anti-HLA Antibody tests performed at the time of donation. |
|
| 2 months |
| Measure the association between the type and precocity of obstetrical complications according to the type of anti-HLA Ab (class I and/or class II), when these Ab are found during the screening test performed by the EFS |
| 2 months |
| Verify the absence of response bias by comparing the HLA Ab levels of responding versus non-responding donors. | Anti-HLA antibody rate (median) | 2 months |