Sanford Health: Ten Children’s Hospitals Now Sharing Genomic Medicine
Three more hospitals have signed on to rapidly integrate genetics and genomics into primary and specialty pediatric care through an innovative consortium with
The new hospitals are Lucile Packard Children's Hospital Stanford,
The mission of the
The other member hospitals include Sanford Children's (
Previous innovation projects funded by the consortium include a study of the outcomes of rapid whole genomic sequencing in critically ill newborn infants, and a study evaluating the routine use of an extensive, pediatric-focused, next generation sequencing panel in the diagnosis of childhood cancers.
Genetic diseases are a leading cause of morbidity and mortality in infants in Neonatal and Pediatric Intensive Care Units (NICU, PICU). These children often undergo an extensive and expensive diagnostic process that may not lead to a final diagnosis.
"The future of pediatric medicine is being transformed by the ability to rapidly decode the genomes of the most fragile newborns to deliver exact diagnoses and targeted treatment," Kingsmore said.
Pediatric cancers have different genetic origins compared with adult cancers. Current panels for detecting the genetic origins of a tumor primarily focus on adult cancers. OncoKids(R) developed at Children's Hospital Los Angeles, is specifically formulated to detect the genomic alterations of pediatric cancers including leukemias, lymphomas, bone, soft tissue and brain tumors.
"The ability to identify the precise underlying genomic alterations in individual tumors with OncoKids(R) allows us to personalize care and innovate how we treat children with cancer," said
Extending precision medicine to children's health through this consortium is inspired by the vision of
"We are thrilled to welcome these three additional premier children's hospitals to the
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