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Preterm and small-for-gestational-age (SGA) infants are more susceptible to vaccine-preventable diseases. To evaluate routine vaccination timeliness in these high-risk groups, a full birth cohort of infants ( = 41,502) born in 2017 and 2018 in Tuscany was retrospectively followed up until 24 months of age. Infants were classified by gestational age (GA) and SGA status. The vaccinations included: hexavalent (HEXA), measles-mumps-rubella, varicella, pneumococcal conjugate (PCV), and meningococcal C conjugate. Time-to-event (Kaplan-Meier) analyses were conducted to evaluate the timing of vaccination according to GA; logistic models were performed to evaluate the associations between GA and SGA with vaccination timeliness. Time-to-event analyses show that the rate of delayed vaccine receipt increased with decreasing GA for all the vaccinations, with a less marked gradient in later vaccine doses. Compared to full-term infants, very preterm infants significantly showed an increased odds ratio (OR) for delayed vaccination in all the vaccinations, while moderate/late preterm infants only showed an increased OR for HEXA-1, HEXA-3, PCV-1, and PCV-3. SGA infants had a significantly higher risk of delayed vaccination only for HEXA-1 and PCV-1 compared to non-SGA infants. In conclusion, vaccinations among preterm and SGA infants showed considerable delay. Tailored public health programs to improve vaccination timeliness are required in these high-risk groups.
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http://dx.doi.org/10.3390/vaccines10091414 | DOI Listing |
Diabetes Technol Ther
September 2025
Disciplina de Obstetricia, Departamento de Obstetricia e Ginecologia da Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sao Paulo, Brazil.
To assess the relationship between time in range (TIR), extrapolated from self-monitoring of blood glucose (SMBG) measures, and adverse perinatal outcomes in pregnant women with type 1 diabetes (T1D). A retrospective cohort study was conducted, including singleton pregnancies that began antenatal care before 20 weeks of gestation and delivered live newborns without malformations between 2010 and 2019. Glycemic data from SMBG were categorized into TIR (63-140 mg/dL or 3.
View Article and Find Full Text PDFFront Med (Lausanne)
August 2025
Department of Obstetrics, The Sixth Affiliated Hospital of Jinan University, Dongguan, China.
Objective: To explore the predictive value of peak systolic velocity (PSV) ratio, PSV1 and PSV2 of ophthalmic artery Doppler in pregnant women for small for gestational age (SGA) infants and to construct a nomogram prediction model.
Methods: A total of 201 pregnant women who visited our hospital from March 2022 to June 2024 were selected as the research subjects, and their clinical data and ophthalmic artery Doppler parameters were collected. The data were randomly divided into a training set ( = 295) and a verification set ( = 126) in a 7:3 ratio.
Pediatrics
September 2025
Vermont Oxford Network, Burlington, Vermont.
Objective: Among extremely low-birth-weight (ELBW; <1000 g) or extremely preterm (EPT; <28 + 0 weeks) infants, we aimed to describe size indicators at 18 to 24 months of corrected age and growth from neonatal intensive care unit (NICU) discharge to follow-up and to examine infant and maternal determinants of those outcomes.
Methods: We studied 7301 ELBW/EPT children from 77 Vermont Oxford Network member hospitals. Continuous size indicators at 18 to 24 months were z scores of weight, length, head circumference, and body mass index based on World Health Organization standards.
J Neonatal Perinatal Med
May 2025
Mother and Child Care Research Center, Hamadan University of Medical Sciences, Hamadan, Iran.
BackgroundDue to the scarcity of available data on the association between isolated oligohydramnios and the risk of small for gestational age (SGA), we undertook a meta-analysis to investigate this relationship.MethodsPubMed (Medline), Web of Science, Scopus, and Science Direct were systematically queried up to February 26, 2024. Analysis was conducted using the random-effects model.
View Article and Find Full Text PDFBMC Pregnancy Childbirth
September 2025
Division of Epidemiology and Biostatistics, School of Public Health, University of Cape Town, Falmouth Building, Anzio Road, Observatory , Cape Town , Western Cape , 7925, South Africa.
Background: Despite improved health and survival due to lifelong antiretroviral therapy (ART), women living with HIV (WHIV) still face lower life expectancy, partly due to increased non-communicable disease (NCD) risk. Both HIV and NCDs are linked to adverse birth outcomes, yet data on their combined impact are limited. We investigated NCD burden by HIV status and compared adverse birth outcomes in pregnant WHIV only versus HIV-NCD comorbidity in Cape Town, South Africa.
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