Volume 68, Issue 3 | Page 9

to call it. MIS-C (multisystem inflammatory syndrome in children, pronounced “miss see”) seems to be the name that has stuck and is most common in the literature now. It is often described as a “mixture of Kawasaki syndrome and toxic shock.” The symptoms are vague: a child of any age with fever for several days, sometimes rash, severe abdominal pain, diarrhea, malaise. And then they may crash, sometimes to the point of needing life support with ECMO. Severity is over a spectrum and sometimes continues to worsen despite correct treatment. The actual mortality rate is still being defined, but we knew in May that it was killing children. With the high rates of asymptomatic pediatric cases of COVID-19, there may not have been a telltale preceding illness that might have prompted testing, and the knowledge that the child was in the pool of potential victims of this secondary syndrome. MIS-C is considered to be a rare disease, but it is a zebra hiding in a herd of galloping horses. In late spring, our regional seasonality also brings more enterovirus and tick-borne infections, which have strikingly overlapping features. Even in the middle of a viral pandemic, kids still get UTIs, salmonella, appendicitis and traditional Kawasaki disease. The next challenge was to try to learn to hear this strange beast in the midst of the cacophony of hoofbeats. So pediatricians did what we always do when confusing febrile diseases present themselves: we called infectious disease and rheumatology to the bedside. Indeed, the protocols and guides coming out of the U.K., New York and other places all called for multi-specialty teams to evaluate, care for the patient and to make decisions on resource utilization for treatment. The protocol workup requires many, many labs, often trended over time as well as ECHO and ECG. The parents are understandably stunned by the amount of blood we are taking from their sick children and confused when infectious disease, rheumatology and cardiology all troop in to see their previously healthy kids. However, even with the vast array of test results in hand, the diagnosis is not simple. Many of the guidelines give decision tree branch points for “abnormal” labs but do not give a scope of how elevated or depressed a value should be to prompt real concern. Additionally, despite 10 years practicing as a pediatric hospitalist, I simply don’t have the context to know what some markers, such as troponin or IL-6, typically do in a pediatric patient with a febrile UTI because we don’t send troponin or IL-6 on these children. So, in vivo, we rely on communication among all the specialists to confirm a diagnosis and make a treatment plan. good bedside care to the patient, coordinate the specialists and find the alternate diagnosis “off-ramp” if possible. The mainstays of treatment, besides symptomatic care, were anticoagulation, steroids and IVIG, depending on the severity of disease. There were difficult conversations with families to explain why we were doing all the workup and the potential outcomes. I think the hardest day was having to tell a mom that whatever precautions they had taken to isolate, they had not been successful. The child most certainly had SARS-CoV-2 infection (as shown by antibody testing). We discussed how she needed to monitor her newborn and her elderly grandmother at home, while dealing with the diagnosis of MIS-C in the older child. I could see in her face her worry that she would lose everyone she loved all at once and there would be nothing she could do about it now. It was difficult to convey my compassion while covered head to toe with face shield, mask, gown and gloves, but I did my best. It was a tiring week. Thankfully, everyone on my service got better instead of worse. We had learned a bit more about the disease, created ways to exit the testing protocols when MIS-C seemed unlikely and worked together across specialties to communicate as a team. I had never had to learn about and treat a completely new disease entity in real time before. MIS-C remains a diagnosis that causes consternation and concern, but we are climbing the steep learning curve as a team, across specialties and the world, to continue the mission to keep kids healthy during this unprecedented pandemic. References PEDIATRICS Article referenced (UK case series with 8 patients) : https://www.thelancet.com/ journals/lancet/article/PIIS0140-6736(20)31094-1/fulltext Article just released describing disease in New York City, including the hospital where Dr Kingery worked: https://www.nejm.org/doi/full/10.1056/NE- JMoa2021756 Most recent article describing MIS-C in the US: https://www.nejm.org/doi/ full/10.1056/NEJMoa2021680?query=recirc_curatedRelated_article (U of L/Norton Children’s Hospital have contributed to this cohort data) CDC diagnostic and treatment guidelines for providers as of 7/1/2020: https:// www.cdc.gov/mis-c/hcp/ Dr. Hodge is a practicing pediatric hospitalist at Norton Children’s Hospital. She is also an Associate Professor in the Department of Pediatrics at the University of Louisville School of Medicine and Director of the Global Education Office (non-member). All this came in to play my next week on service. Concern in the community was so high that it seemed like any child with a fever for more than 24 hours was getting worked up for MIS-C in the office or emergency department and sent to us. Frightened parents were Googling the new disease and becoming filled with dread. New guidelines were published nearly every other day, and it was difficult to feel knowledgeable and confident that you were doing the right things. My main jobs as a hospitalist were to give AUGUST 2020 7