Assess the Correlation With Severe Respiratory Syncytial Virus Disease in the First 6 Months in Children With Congenital Heart Disease and Maternal Ac-AntiVSR Titers During Pregnancy
NCT ID: NCT04734782
Last Updated: 2021-02-02
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
60 participants
OBSERVATIONAL
2021-02-15
2022-03-31
Brief Summary
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Justification
The most serious evolution of the clinical disease of acute RSV bronchiolitis in children under 6 months of age is related to lower exposure of the pregnant woman to the RSV epidemic. With maternal immunization through natural exposure, it is logical to relate protection to children for severe RSV disease. However, it is not proven (3).
1. \- Nandapalan N, Taylor CE, Greenwell J, et al. Seasonal variations in maternal serum and mammary immunity to RS virus. J Med Virol. 1986;20(1):79-87. doi:10.1002/jmv.1890200110
2. \- Stensballe LG, Ravn H, Kristensen K, Meakins T, Aaby P, Simoes EA. Seasonal variation of maternally derived respiratory syncytial virus antibodies and association with infant hospitalizations for respiratory syncytial virus. J Pediatr. 2009;154(2):296-298. doi:10.1016/j.jpeds.2008.07.053
3. \- Ramos-Fernández JM, et al. Does exposure of pregnant women to epidemic respiratory syncytial virus affect the severity of bronchiolitis? Enferm Infec Microbiol Clin. 2017. https://doi.org/10.1016/j.eimc.2018.07.002)
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Detailed Description
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According to the IGG titers in anti-RSV serum, 2 groups will be formed:
Protective Mothers (high IGG titers) Non-protective mothers (low IGG titers) The products will be followed up for 6 months after birth to correlate the maternal titers of Ac anti-RSV with the presence and severity of respiratory infection by RSV (Bronchiolitis) in this period.
Population and period
Pregnant women evaluated in the National Medical Center 20 de Noviembre, Pediatric Cardiology service for the prenatal diagnosis of congenital heart disease in their fetuses. Newborns with corroborated congenital heart disease with prenatal diagnosis.
Study inclusion period February 1, 2021, to October 30, 2021. Study follow-up period March 1 2021 to December 30 2021.
Sample type: Non-randomized, for convenience, sequential and with an estimated of 30 patients per group.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Protective Mothers (high IGG titers)
Protected group Newborns with congenital heart disease + high titers of anti-RSV IGG in the mother's serum before birth
Determination of antibodies in maternal serum IgG for respiratory syncytial virus
By venipuncture, a blood sample will be taken and the levels of anti-RSV IgG antibodies will be processed in serum by commercial techniques.
Non-protective mothers (low IGG titers)
Unprotected group Newborn with congenital heart disease + negative anti-RSV IGG titers in the mother's serum before birth.
Determination of antibodies in maternal serum IgG for respiratory syncytial virus
By venipuncture, a blood sample will be taken and the levels of anti-RSV IgG antibodies will be processed in serum by commercial techniques.
Interventions
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Determination of antibodies in maternal serum IgG for respiratory syncytial virus
By venipuncture, a blood sample will be taken and the levels of anti-RSV IgG antibodies will be processed in serum by commercial techniques.
Eligibility Criteria
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Inclusion Criteria
2. Approval of informed consent
3. Newborn of term or preterm, with corroborated congenital heart disease and presenting with a respiratory infection by RSV
Exclusion Criteria
2. \- Premature birth and need for neonatal intensive care for more than 4 weeks.
3. \- Newborn with bronchopulmonary dysplasia
Elimination criteria
1.- Use of palivizumab
1 Month
12 Months
ALL
No
Sponsors
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Hospital Angeles Lomas
OTHER
Responsible Party
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Humberto Garcia Aguilar
Master in Science
Locations
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Centro Medico Nacional 20 de Noviembre
Mexico City, , Mexico
Countries
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Other Identifiers
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025.2021
Identifier Type: -
Identifier Source: org_study_id
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