Study Suggests Routine Newborn Screening for Cytomegalovirus Could Detect More Cases
A three-year study conducted at Hadassah Medical Center in Jerusalem, led by Dana Wolf, Smadar Eventov Friedman, and Moran Yassour, indicates that routine newborn screening for congenital cytomegalovirus (cCMV) could significantly increase detection rates. The study, published in The Lancet Infectious Diseases, screened 48,556 newborns, identifying 176 infants with cCMV, which translates to approximately 3.6 cases per 1,000 babies. A key finding was that 57% of these cCMV cases (100 out of 176) would have gone undetected under the more common targeted screening approach, which typically tests babies only when there are suspicious signs like a failed hearing test or known maternal infection. Among these 100 babies who appeared healthy at birth, eight later developed moderate to severe cCMV signs, and three experienced hearing loss despite initially being asymptomatic. Eleven ultimately received antiviral treatment. The researchers utilized a pooled saliva-testing system, adapted from a COVID-19 PCR testing ...