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An In vitro Model to Study Immune Responses of Human Peripheral Blood Mononuclear Cells to Human Respiratory Syncytial Virus Infection
Published on: December 10, 2013
Risk Factors for Severe Respiratory Syncytial Virus Infection in Hospitalized Children
Hsuan-Yin Ma1,2, I-Fan Lin2, Yun-Chung Liu2
1From the Center for Drug Evaluation, Taipei, Taiwan.
Insights
Infants under 1.5 months with heart or genetic conditions face higher risks of severe respiratory syncytial virus (RSV) infections. Early intervention with RSV monoclonal antibody (RSV mAb) prophylaxis may be beneficial.
Area of Science:
- Pediatrics
- Infectious Diseases
- Public Health
Background:
- Respiratory syncytial virus (RSV) frequently causes severe respiratory illness in infants.
- High-risk infants, including premature and those with congenital heart disease, are candidates for RSV prevention.
- Further investigation into risk factors beyond prematurity and congenital heart disease is needed.
Purpose of the Study:
- To identify risk factors for severe RSV infection in hospitalized children.
- To evaluate the impact of RSV monoclonal antibody (RSV mAb) endorsement on severe RSV outcomes.
Main Methods:
- A cohort study was conducted at National Taiwan University Hospital from 2008 to 2018.
- Severe RSV infection was defined as requiring invasive ventilator support.
- Risk factors were identified using multivariable analysis, adjusting for age, sex, and birth cohort.
Main Results:
- Out of 1985 RSV admissions, 66 (3.3%) experienced severe RSV infection.
- Severe RSV infections significantly decreased post-RSV mAb endorsement.
- Key risk factors included age <1.5 months, cardiovascular diseases, congenital/genetic diseases, bacterial coinfections, elevated creatinine, and abnormal chest X-rays.
Conclusions:
- Infants younger than 1.5 months with cardiovascular or congenital/genetic conditions are predisposed to severe RSV.
- RSV mAb prophylaxis may offer significant benefits for these high-risk infants.
Background:
Respiratory syncytial virus (RSV) is a common cause of bronchiolitis and pneumonia in infants and young children. Starting in December 2010, RSV monoclonal antibody (RSV mAb) was endorsed by Taiwan National Health Insurance and given to children with prematurity and/or congenital heart diseases, which are considered high-risk factors for severe RSV diseases. Investigating other important contributing risk factors is warranted.
Methods:
We conducted a cohort study at National Taiwan University Hospital to determine the rate of severe outcomes among children hospitalized due to RSV infection from 2008 to 2018. Adjusted for age, sex and birth cohorts born before and after RSV mAb endorsement, we identified risk factors for severe RSV infection, defined as the requirement of invasive ventilator support.
Results:
There were 1985 admissions due to RSV infections. Among them, 66 patients (3.3%) had severe RSV infection. The proportion of severe RSV infections decreased significantly after RSV mAb endorsement. Multivariable analysis revealed that age <1.5 months and cardiovascular and congenital/genetic diseases were high-risk underlying conditions. In addition, bacterial coinfections, elevated creatinine levels and initial abnormal chest radiograph findings posed warning signs for severe RSV infection.
Conclusions:
Children younger than 1.5 months of age with cardiovascular or congenital/genetic diseases were predisposed to severe RSV infection and might benefit from RSV mAb prophylaxis.
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