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| ID | Type | Description | Link |
|---|---|---|---|
| 2019-A02623-54 | Other Identifier | ID-RCB Number |
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Study manager's decision
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| Name | Class |
|---|---|
| Filière des Maladies Rares Abdomino-THOraciques : FIMATHO | UNKNOWN |
| URC-CIC Paris Descartes Necker Cochin | OTHER |
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The objective is to evaluate the quality of the response to the Blood Oxygen Level Dependent effect in fetuses with diaphragmatic hernias and abdominal wall malformations and to correlate with postnatal respiratory outcome. Pulmonary involvement is a constant in diaphragmatic hernias, it is classic in omphaloceles and especially hepatomphaloceles, and exceptional in laparoschisis. As this is an original exploratory study, no preliminary data are available.
If a correlation is found, the Blood Oxygen Level Dependent effect of the fetal lung may be considered as an early functional marker of postnatal lung function. It can be used in addition to lung-to-head-ratio during prenatal counseling.
The final goal is to be able to detect early in the fetus pulmonary insufficiency to help prenatal counseling and perinatal care.
During the fetal period, there is in the lungs a permanent flow and pressure variations between the "inhaled" amniotic fluid and alveolar secretions, which are essential for pulmonary development. A disruption of this physiological mechanism can induce disorders of the respiratory function, which go from simple delay of maturation to hypoplasia. Respiratory function involves the thoracic muscles (diaphragmatic and intercostal) but also the abdominal muscles, that explains why breathing difficulties are found at birth in neonates with diaphragmatic hernia but also abdominal wall malformations.
This pulmonary involvement highly contributes to the morbidity observed at birth, for which strong prenatal predictive criteria are lacking.
Pulmonary volume measurement by the lung-to-head-ratio is widely used for diaphragmatic hernia has been extended to other congenital malformations, because no other available criteria. The lung-to-head-ratio is a parameter well correlated with survival but insufficiently with morbidity and sequelae.
New functional imaging techniques are in development. Among them, the Blood Oxygen Level Dependent uses hemoglobin as an endogenous contrast agent. It is based on the comparison of a basic status in ambient air with status after oxygenation. It gives a functional evaluation of the organs. But this technique has never been evaluated in the fetal lung yet.
The objective of the study is to evaluate the quality of the response to the Blood Oxygen Level Dependent effect in fetuses with diaphragmatic hernias and abdominal wall malformations and to correlate with postnatal respiratory outcome. It is an original exploratory study and no preliminary data are thus available.
If a correlation is found, the Blood Oxygen Level Dependent effect of the fetal lung may be considered as an early functional marker of postnatal lung function. It could then be used in addition to lung-to-head-ratio during prenatal counseling. The final goal is to be able to detect early in the fetus pulmonary insufficiency to help prenatal counseling and perinatal care.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Congenital diaphragmatic and parietal malformations | Experimental | Patients with fetal magnetic resonance imaging as part of their usual medical care, for fetal / placental indications of diaphragmatic hernia, omphalocele or gastroschisis. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Functional magnetic resonance imaging - Blood Oxygenation Level Dependent | Diagnostic Test | First Functional magnetic resonance imaging - Blood Oxygenation Level Dependent sequence under ambient air. Oxygenation of 5 minutes at a rate of 12 l / min. Second Functional magnetic resonance imaging - Blood Oxygenation Level Dependent sequence. |
| Measure | Description | Time Frame |
|---|---|---|
| Value of the Blood Oxygenation Level Dependent of the fetal lung | Regions of interest (ROI) were manually identified on MRI images, with the largest possible homogenous 2D area. For the lungs, the ROIs were delineated at the maximal chest circumference, delineating the right lung, the left lung. Changes in haemoglobin concentration will be evaluated by the variation in transverse R2* signal induced by oxygenation in the delimited ROI. The BOLD response will be calculated for each case as the difference between normoxic and hyperoxic period (∆R2*) normalized by normoxic value: ∆R2* = [R2*(norm)-R2*(hyper)] / R2*(norm). | 30 months |
| Postnatal respiratory evolution | Duration of mechanical ventilation | 30 months |
| Measure | Description | Time Frame |
|---|---|---|
| Postnatal survival | Survival rate at 30 days after birth | 30 months |
| Duration of oxygen dependence | Total days of oxygen requiring | 30 months |
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Inclusion Criteria:
Exclusion Criteria:
Pregnant patients
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| Name | Affiliation | Role |
|---|---|---|
| Naziha KHEN-DUNLOP, MD, PhD | Assistance Publique - Hôpitaux de Paris | Principal Investigator |
| Laurent SALOMON, MD | Assistance Publique - Hôpitaux de Paris | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Hôpital Necker-Enfants Malades | Paris | 75015 | France |
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| Length of hospitalization | Total days of the neonatal hospitalization before discharge | 30 months |
| ID | Term |
|---|---|
| D065630 | Hernias, Diaphragmatic, Congenital |
| D006554 | Hernia, Umbilical |
| D020139 | Gastroschisis |
| D012131 | Respiratory Insufficiency |
| ID | Term |
|---|---|
| D000013 | Congenital Abnormalities |
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| D006548 | Hernia, Diaphragmatic |
| D000082122 | Internal Hernia |
| D006547 | Hernia |
| D020763 | Pathological Conditions, Anatomical |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D007232 | Infant, Newborn, Diseases |
| D006555 | Hernia, Ventral |
| D046449 | Hernia, Abdominal |
| D009139 | Musculoskeletal Abnormalities |
| D009140 | Musculoskeletal Diseases |
| D012120 | Respiration Disorders |
| D012140 | Respiratory Tract Diseases |
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