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In Belgium, labour epidural analgesia (LEA) has been used for decades in the vast majority of vaginal deliveries (up to 83% of deliveries). Labour epidural analgesia is the most effective and safest way to allow pregnant women a nearly pain-free labour- and birth experience. Recent data showed that the use of LEA was associated with a reduced risk for severe maternal morbidity, neonatal resuscitation and with a reduced risk for low Apgar scores. However, prenatal exposure to labour epidural analgesia has been associated by several study groups with an increased risk for autism spectrum disorder (ASD) in the children, but these studies suffer from several important limitations which may have induced significant bias (e.g., not correcting for unmeasured confounders). Associations with other neurodevelopmental disorders (e.g., Attention Deficit Hyperactivity Disorder (ADHD), oppositional defiant disorder (ODD) and conduct disorder (CD)) and cognitive functioning have not been investigated yet. There is hence an urgent need for a study allowing definitive conclusions by overcoming the limitations of the previous studies. The investigators will perform the first sibling-matched clinical cohort study using a prospective investigator-assessment of multiple domains of cognitive functions. The investigators hypothesize that prenatal exposure to LEA will neither be associated with reduced intelligence nor with more neurodevelopmental disorders. Validating this hypothesis holds the potential to grant women the assurance to confidently receive the most efficacious method for labour analgesia, free from apprehension that it might have adverse implications for their children's neurodevelopment.
Primary objective:
To compare the intelligence of children prenatally exposed to labour epidural analgesia with that of sibling matched unexposed children.
Secondary objective(s):
To compare parentally reported traits of ASD, ADHD, ODD and CD of children prenatally exposed to labour epidural analgesia with that of sibling matched unexposed children.
Endpoints:
Sample size:
At least 64 prenatally exposed children and 64 prenatally unexposed children
Summary of eligibility criteria:
Dutch speaking sibling pairs discordant for prenatal exposure to labour epidural analgesia will be included. Children born from 1st January 2014 until 1st November 2019 will be included. Children prenatally exposed to maternal surgery, foetal surgery/interventions, chemotherapy, radiotherapy, radiology and oncologic pathology will be excluded. Children with a diagnosis of severe disability of genetic origin (e.g., Fragil X, Down syndrome,…), history of head trauma, major congenital birth defects, children born at a gestational age < 37 weeks or > 42 weeks, or with a birth weight < 2.5 kg will be excluded. Children exposed to general anaesthesia after birth, twins/triplets/multiple births will be excluded. Elective and intrapartum caesarean sections will be excluded.
Maximum duration a research subject remains in the study:
Study will be conducted in 2024-2027. The end of the study for each individual participant is determined by the date at which the neuropsychological testing is planned. Neuropsychological testing usually takes no longer than 2 hours.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Exposed | Children prenatally exposed to labour epidural analgesia |
| |
| Unexposed | Prenatally not exposed to labour epidural analgesia |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Labour epidural analgesia | Procedure | Prenatal exposure to labour epidural analgesia during delivery |
|
| Measure | Description | Time Frame |
|---|---|---|
| Wechsler full-scale intelligence quotient | Will be assessed using the Wechsler Intelligence Scale for Children (WISC). Minimum value: 40, maximum value: 160. Higher scores mean a better outcome. | At te moment of neuropsychological testing |
| Measure | Description | Time Frame |
|---|---|---|
| Indices of the Wechsler intelligence scale | Verbal comprehension, working memory, visual spatial, fluid reasoning, processing speed. Minimum value: 40, maximum value: 160. Higher scores mean a better outcome. | At te moment of neuropsychological testing |
| Clinically relevantly decreased intelligence quotient |
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Inclusion Criteria:
Exclusion Criteria:
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Sibling pairs discordant for prenatal exposure to labour epidural analgesia will be included
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Tom Bleeser, MD, PhD | Contact | +3216344270 | tom.bleeser@uzleuven.be |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University Hospitals Leuven | Leuven | 3000 | Belgium |
Can be requested from authors.
Can be requested from authors.
Can be requested from authors.
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot_SAP | Yes | Yes | No | Study Protocol and Statistical Analysis Plan | Nov 1, 2024 |
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The absolute risk reduction for a clinically relevantly decreased intelligence quotient, defined as an IQ<85, will be calculated. |
| At te moment of neuropsychological testing |
| Social responsiveness scale (SRS) | Parental reported social deficits in the autism spectrum. Minimum value: 0, maximum value: 195. Higher scores represent a worse outcome. | At te moment of neuropsychological testing |
| Disruptive Behavior Disorders Rating Scale (DBDRS) | Parental reported traits of inattention, hyperactivity and impulsivity (ADHD), oppositional defiant disorder (ODD) and conduct disorder (CD). Minimum value: 0, maximum value: 135. Higher scores mean a worse outcome. | At te moment of neuropsychological testing |
| May 17, 2025 |
| Prot_SAP_000.pdf |