Only 1 in 5 parents plan to get COVID vaccine for kids under 5 when available: survey

Only 18 percent of parents of children under 5 say they plan to get their child vaccinated against COVID as soon as they can, while nearly 4 in 10 say they will "wait and see" before getting shots for their child, a new U.S. survey reveals.

Nearly 3 in 10 (27%) said they would "definitely not" get their child vaccinated and 11% said they would do so only if required, according to the Kaiser Family Foundation's Vaccine Monitor survey released Wednesday.

More than half of parents with children younger than 5 said they "don't have enough information about the safety and effectiveness of COVID-19 vaccines for children in this age group," and about 13% of parents said the U.S. Food and Drug Administration's delay in authorizing a vaccine for this age group made them less confident about its safety, while 22% said it made them more confident.

COVID vaccines for these youngest Americans could come this summer: In April, Moderna asked the U.S. Food and Drug Administration to approve the emergency use of its vaccine in kids under 6. Pfizer continues to gather data on the power of a third shot for kids under 5, after a weak showing in the immune response triggered by two doses prompted the company to wait for results from three doses in this age group. Data on three doses is expected by June.

Responses from parents of older children were similar to those with young kids.

Among parents of children ages 5-11, 39% said their children were already vaccinated while 32% said their children would definitely not be vaccinated. Among parents of children ages 12-17, the rates were 56% and 31%, respectively.

Concerns about not having enough information about the safety and effectiveness of vaccines for their children were expressed by 34% of parents of children ages 5-11 and 25% of parents of children ages 12-17.

More than 80% of all parents in the survey said they felt their child was very or somewhat safe from COVID-19 while at school, but the rate was higher among white parents (52%) than among Black and Hispanic parents (one third), CNN reported.

When it came to school mask mandates, the percentage of parents who said that their child was required to wear a mask at school fell from 69% in September to 16% in April.

Still, "parents who are Black or Hispanic are more than twice as likely as White parents to say their child usually wears a mask [70% vs. 26%] and five times as likely to say that most other students at their child's school wear masks [9% vs. 47%]," according to the survey authors.

More information: Visit the U.S. Centers for Disease Control and Prevention for more on COVID vaccines for kids.

Copyright © 2022 HealthDay. All rights reserved.

Invasive Group B strep in early infancy associated with higher risk of neurodevelopmental impairment in later life

by London School of Hygiene & Tropical Medicine

Invasive Group B strep in early infancy associated with higher risk of neurodevelopmental impairment in later lifeMulti-domain and domain specific impairment among non-iGBS children, any iGBS, GBS-sepsis, and GBS-meningitis, stratified by country. Proportion of children with different NDI outcomes in South Africa, Mozambique, India, Kenya, and Argentina for GBS exposed and unexposed children. (A) Overall impairment (moderate/severe and mild). (B) Motor impairment (moderate/severe and mild).(C) Cognitive impairment (moderate/severe and mild). (D) Emotional-behavioral problem (any problem in clinical range). (E) Hearing and vision impairment (any impairment). GBS=group B Streptococcus. GBS-M=GBS meningitis. GBS-S=GBS sepsis. NDI=neurodevelopmental impairment. Credit: eClinicalMedicine (2022). DOI: 10.1016/j.eclinm.2022.101358

Children with a history of invasive Group B Streptococcus (iGBS) disease face a higher risk of moderate to severe neurodevelopmental impairment (NDI) later in life compared to non-iGBS children, according to a new study published in eClinicalMedicine.

iGBS is caused by a common bacterium that can be transmitted in the womb, during birth, or in the early weeks of life.

The first multi-country study of its kind on GBS outcomes in low- and middle-income countries was led by the London School of Hygiene & Tropical Medicine (LSHTM) with members of the GBS long term outcomes LMIC collaborative group. It aimed to estimate the risk of NDI for children with a history of iGBS across three regions with a high burden of disease: sub-Saharan Africa, Asia and Latin America.

The study, which included data from South Africa, India, Mozambique, Kenya and Argentina, found that neurodevelopmental impairment was frequent following iGBS in the first 90 days of life. Children with a history of iGBS had a 70% increased risk of any NDI, compared to those without iGBS.

The findings demonstrate a higher than previously recognized burden of NDI in iGBS survivors, emphasizing the urgent need for a maternal vaccine against GBS and calling for increased research into the longer-term outcomes of the disease.

A recent report from the World Health Organization (WHO) and LSHTM revealed the alarming global impact of GBS. An average of 15% of all pregnant women worldwide—nearly 20 million annually—carry the GBS bacterium in their vagina, usually without symptoms. It can then spread from a pregnant woman to her unborn baby in the womb, or to newborns during labor, leading to around 150,000 deaths of babies each year, more than half a million preterm births and significant long-term disability.

Despite wide reporting of neonatal and infant mortality associated with iGBS disease, the impact of iGBS on NDI has been under studied. Data from low- and middle-income countries (LMICs) is particularly lacking, despite the majority of iGBS cases occurring in these countries.

Accurate measurement of NDI is crucial for estimating the burden of disease and cost-effectiveness of preventative approaches.

Dr. Proma Paul, Research Fellow at LSHTM and first author, said: "Our study is the first low- and middle-income multi-country data to show a higher risk of neuro-developmental delays in children surviving invasive GBS infections. These children deserve earlier detection and better healthcare and education for them and their families to thrive. Maternal GBS vaccines could be high impact."

A total of 138 iGBS survivors and 390 non-iGBS children, aged between 1–18 years old, were included in the study. The research team matched children with a history of iGBS to those without in each location by age and sex. Children with a history of iGBS were identified as having experienced either GBS-sepsis or GBS-meningitis in the first 90 days after birth.

Sepsis, a life-threatening reaction to an infection also known as blood poisoning, is the most common clinical presentation of iGBS disease. 74.3% of the iGBS children included in the study had a history of GBS-sepsis, 25.7% had experienced GBS-meningitis.

Of the iGBS surviving children, overall, 38.1% had any NDI (mild, moderate or severe), compared to 21.7% of non-iGBS children. Hence the risk of NDI was increased by 70% compared to unaffected children, matched for age and sex.

Among GBS-sepsis children, the team estimated a 5% risk of moderate/severe NDI later in life. This increased to 15% for GBS-meningitis children. Although the risk of NDI following GBS-sepsis is lower, as it is more common than meningitis, it is likely to contribute to a high portion of the total NDI burden.

Risk of moderate/severe NDI among iGBS survivors varied by location: 2.9% in India, 3.4% in Kenya, 7.7% in Mozambique, 13.9% in South Africa and 23.1% in Argentina. Frequency of mild neurodevelopmental impairment also varied between the countries included in the study, ranging from 18% in Mozambique to 61% in Argentina.

Age-specific culturally appropriate neurodevelopmental assessment tools were used to assess NDI, including motor function, cognition, vision, hearing and emotional-behavioral outcomes. Cognitive impairment was found to be more common among iGBS survivors than motor, hearing and vision impairment in all study countries, except India, where only mild cognitive impairment was detected.

Frequency of emotional-behavioral problems were found to be similar in iGBS children and non-GBS children. Stunting and moderate/severe malnutrition were also assessed but were found to be similar between the iGBS and non-GBS cohorts.

Disability was found to be more common after GBS-meningitis, a finding consistent with previous studies on GBS-meningitis. The study's findings on GBS-sepsis survivors, who also have substantial NDI, are new.

The study highlights the need for freely available standardized developmental assessment tests that can be adapted to context for routine use in both clinical practice and to inform public health policy. Better detection of iGBS is also needed to link to better healthcare and education for affected children and comprehensive support for their families, requiring context-specific implementation research.

The researchers acknowledge that the study has limitations and may not be representative of all iGBS survivors. For example, meningitis is underdiagnosed, especially in neonates, leading to misclassification where meningitis is considered to be sepsis, a common occurrence in low income or resource limited settings.

The "Global Roadmap to Defeat Meningitis by 2030" led by the World Health Organization (WHO) with partners including LSHTM aims to tackle the leading causes of meningitis, including GBS. One of its priorities includes the development of a vaccine against GBS which could be highly cost-effective—with significant health benefits—in all regions of the world. Several GBS vaccine candidates are in development, but none are yet available, despite having been in the pipeline for several decades.

More information: Proma Paul et al, Neurodevelopmental and growth outcomes after invasive Group B Streptococcus in early infancy: A multi-country matched cohort study in South Africa, Mozambique, India, Kenya, and Argentina, eClinicalMedicine (2022). DOI: 10.1016/j.eclinm.2022.101358

Journal information: EClinicalMedicine 

Provided by London School of Hygiene & Tropical Medicine