The purpose of this study is to assess the efficiency of the preventive oxygen therapy on the occurrence of vaso-occlusive complications, which last more than 24 hours and require hospitalisation, in women with sickle cell disease.
Sickle cell disease (SCD) corresponds to a group of inherited disorders with clinical manifestations resulting from the biochemical consequences of a single-base substitution of valine by glutamic acid at position 6 of the ß-hemoglobin (Hb) subunit (HbA \[ß6val\] to HbS \[ß6glu\]). When the oxygen tension is low, the solubility of HbS falls and the molecules polymerize. In turn, the intracellular formation of HbS polymers results in red blood cell (RBC) sickling. The aggregation of sickle cells is responsible for the vaso-occlusive crises (VOCs) that characterize SCD. Thanks to improvements in the management of SCD patients, over 95% of affected infants survive to adulthood. Pregnancy is a high-risk situation for women with sickle cell disease, especially in the third trimester, during delivery and in the post-partum period. Conversely sickle cell disease can lead to pregnancy complications for both mother and fetus since maternal-fetal mortality remains elevated. RBC transfusions and careful prevention of infections represent the only available treatments in this situation. The complexity of this setting and the associated therapeutic strategy is further accentuated by the high frequency of post-transfusion side effects during SCD pregnancies, can indirectly affect the newborn by inducing hypoxia, and may ultimately prevent the woman from receiving further transfusions (RCOG, 2015) (Tuck et al, 1983). Post-transfusion complications constitute negative prognostic factors that affect both the mother's health and fetal development and thus increase the risk of premature death. Another factor complicating the outcome of the pregnancy is the increase in oxygen demand in order to satisfy the increased metabolic requirements of the placenta and fetus. As the maternal oxygen reserve can be compromised during pregnancy for several reasons (such as the increased oxygen consumption, the SCD related anemia accentuated by the plasmatic increase), patients are particularly susceptible to hypoxemia - leading to the exacerbation of sickling events and SCD-related complications. (Hill \& Pickinpaugh, 2008)(Thame et al, 2007)(Rathod et al, 2007a)(Cines et al, 1998)(Hassell, 2005)(Pantanowitz et al, 2000)(Rathod et al, 2007b) Moving from this observation, the first innovative approach introduced was the widespread use of prophylactic oxygen treatment at home. The rationale behind this change came from experiments on a murine model of SCD mice, in which a high-oxygen environment during pregnancy was associated with a lower prenatal fetal/maternal mortality rate (Ye et al, 2008). The absence of severe complications was also noticed in some women who could not be transfused (because of severe alloimmunization) and who were already receiving oxygen therapy at home before pregnancy. Then a preliminary retrospective study was performed to evaluate the clinical benefit of the widespread use of prophylactic oxygen treatment at home. It indicates that this innovative treatment is safe and seems to be associated with a significant decrease in the transfusion rate in SCD patients during pregnancy. These findings are encouraging, but they are preliminary and bias have to be taken into account. These results have to be confirmed by a randomized trial. The project aim is to assess preventive oxygen therapy impact on women with sickle cell disease, their fetal and their newborn. Firstly, investigators want to assess preventive home-based oxygen therapy efficacy for preventing vaso-occlusive complications which last 24 hours and require a hospitalization. Secondly, they want to assess oxygen therapy impact on prevention and characteristics of obstetrical complications, prevention of neonatal complications, fetal and newborn's characteristics, type of medical care, transfusion balance sheet, way of transfusion and maternal, fetal and newborn tolerability of home-based oxygen therapy during pregnancy. For this they propose to analyze 200 pregnant SCD women. 100 women in the first arm with standard medical care. 100 women in the second arm who will have home-based oxygen therapy early at night. This study will be performed in 9 French hospitals. Blood samples of SCD women and blood cord will be drawn to monitor red cell adherence protein expression and function and their mechanic and adhesive properties.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Enrollment
178
Oxygen therapy early in the night (2L/min) during 4hours per days
Hôpital Necker Enfants-Malades (Public Hospitals of Paris)
Paris, Paris, France
Occurrence of at least one vaso-occlusive complication which last more than 24h
Painful vaso-occlusive episodes in bones, acute chest syndrome, ischemic stroke, cardiomyopathy, pulmonary hypertension, splenic and hepatic sequestration, death of the mother
Time frame: 30 days postpartum
Occurrence of at least one vaso-occlusive complication which last more than 24h
Painful vaso-occlusive episodes in bones, acute chest syndrome, ischemic stroke, cardiomyopathy, pulmonary hypertension, splenic and hepatic sequestration, death of the mother
Time frame: 30 days postpartum
Occurrence of pregnancy-induced hypertension, pre-eclampsia, eclampsia
Time frame: 20 months
Occurence of hospitalisation because of premature delivery risk
Time frame: 20 months
Occurence of late miscarriage
Time frame: 20 months
Occurence of Preterm (<35SA) and very preterm ( from 26 to 32SA)
Time frame: 20 months
Type of delivery (vaginal, active, caesarean)
Time frame: 20 months
Number of days hospitalisation postpartum
Time frame: 20 months
Occurence of Neonatal complications ( respiratory distress, analgesics withdrawal symptom)
Time frame: 20 months
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Number of days of hospitalisation for the newborn
Time frame: 20 months
Number of days of hospitalisation in resuscitation unit for the newborn
Time frame: 20 months
Newborn weight
Time frame: 20 months
Newborn size
Time frame: 20 months
Newborn head circumference
Time frame: 20 months
Apgar score assess 1 min after birth
Time frame: 20 months
Apgar score assess 5 min after birth
Time frame: 20 months
Apgar score assess 10 min after birth
Time frame: 20 months
Perinatal and neonatal death
Time frame: 20 months
pH of of the newborn
Time frame: 20 months
Lactate of of the newborn
Time frame: 20 months
Number of days using painkiller (level II and III) during pregnancy
Time frame: 20 months
Number of urgent consultation
Time frame: 20 months
Number of days of hospitalisation and hospitalisation in intensive care during pregnancy
Time frame: 20 months
Stage of pregnancy at the first transfusion
Time frame: 20 months
Total volume of transfusion during pregnancy
Time frame: 20 months
Way of transfusion: simple, bleeding-transfusion, erythrocytapheresis
Time frame: 20 months
Maternal, fetal and newborn tolerability of home-based oxygen therapy during pregnancy
Time frame: 20 months