Children with Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) have high rates of complications — resulting in long and costly hospital stays — and that treatment strategies varied among health care providers, according to the first large-scale analysis, which is published in the Journal of Allergy and Clinical Immunology: In Practice.
In contrast to adults, death and recurrence are rare in children, the study showed.
“These are conditions that doctors fear because the disease can be extremely severe and there is a lack of research to guide treatment decisions,” says James Antoon, MD, PhD, assistant professor of pediatrics in the University of Illinois at Chicago College of Medicine, in a news release. “We know that children with SJS and TEN can have life-long physical and psychiatric effects, but because cases are rare and unpredictable, rigorous studies to evaluate treatments have been difficult to design and implement.”
To fill this gap, Dr. Antoon and his colleagues performed a retrospective analysis of data from the Pediatric Health Information System to describe a cohort of hospitalized children diagnosed with SJS or TEN between 2008 and 2015. Nearly 900 patients, with a mean age of 10, were included in the final analysis, which included a review of treatments, cost of hospital care, length of hospital stay, mortality, recurrence, hospital readmission and complications related to SJS or TEN, in addition to demographic information like age, race, gender, insurance type and geographic location.
They found overall mortality to be low — only 0.56 percent of children died from SJS or TEN, compared with up to 23 percent of adults, as reported in other studies — but nearly one in four pediatric patients was admitted to an intensive care unit. The median length of stay was eight days and readmissions were common, with nearly one in five patients being admitted back to the hospital within six months. Cost of care ranged from about $7,000 to $34,000, with a median cost of adjusted hospital charges of about $16,000 per patient.
“Our finding of low mortality differs from prior, smaller studies performed in the pediatric population,” Dr. Antoon says. “This is helpful information for physicians counseling families. This means that when we talk with parents, we have evidence to help inform families on expectations and overall prognosis.”
The study results, he says, also provide valuable information clinicians can use to guide treatment decisions. When treatments were compared, the researchers found that outcomes were similar across all interventions despite some, like antibody treatments, being significantly more costly.
“There was an expected amount of inconsistency in the treatment of SJS and TEN; however, our analysis showed that no single agent or combination treatment was best at treating SJS and TEN,” Dr. Antoon says. “This is the first large-scale evidence to suggest we can potentially reduce the cost of care for families by selecting lower-cost treatments to achieve the same outcomes.”
The most common treatment was intravenous immunoglobulin (IVIG) in 25 percent of patients, followed by steroids in 18 percent, and a combination of both IVIG and steroids in 17 percent of children.
“Yet, there was little difference in outcomes such as mortality, length of hospital stay, or need for life support across treatments,” Dr. Antoon says.
The treatments, the researchers found, varied by geography. Patients receiving care in the Middle Atlantic and East North Central geographic regions were more likely to receive more expensive combination therapies (26 percent and 24 percent, respectively), compared with patients in the West North Central (only 8 percent) region.
“Overall, these findings suggest we can be cautiously optimistic about SJS and TEN outcomes in a pediatric population,” Dr. Antoon says, “but that we need more research to dig deeper into strategies that reduce complications, hospital stays and even the cost of care.”
Co-authors on the paper are Jennifer Goldman and Brian Lee of Children’s Mercy Hospital and Clinic in Kansas City, Missouri, and Samir Shah of Cincinnati Children’s Hospital Medical Center. Goldman’s work was supported in part by a grant (KL2TR000119) from the National Center for Advancing Translational Sciences, part of the National Institutes of Health.
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