Tight glycemic control after pediatric heart surgery shows no benefit

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Tight glycemic control can be achieved in children following cardiac surgery, but it does not reduce the infection rate, mortality, or length of hospital stay compared to standard care, according to a study published in the September 7 issue of The New England Journal of Medicine

Tight glycemic control can be achieved in children following cardiac surgery, but it does not reduce the infection rate, mortality, or length of hospital stay compared to standard care, according to a study published in the September 7 issue of The New England Journal of Medicine.

The 2-center, prospective, randomized trial, led by Michael S.D. Agus, MD, with Boston Children’s Hospital, consisted of 980 children who were aged 0 through 36 months. The patients were randomly assigned to receive either tight glycemic control or standard care in the cardiac intensive care unit (ICU).

Of the 490 children assigned to tight glycemic control, 444 (91%) received insulin versus 9 (2%) of 490 children who were assigned to standard care.

The researchers found that normal glucose levels were achieved earlier with tight glycemic control than with standard care (6 hours vs 16 hours, P<.001) and were maintained for a greater proportion of the critical illness period (50% vs 33%, P<.001). However, tight glycemic control was not associated with a significantly decreased rate of healthcare–associated infections (8.6 per 1,000 patient-days in the tight glycemic control group compared with 9.9 per 1,000 patient-days in the standard of care group; P=.67). In addition, mortality, length of hospital stay, organ failure, and hypoglycemia rates did not differ significantly between the groups.

“Our trial showed that tight glycemic control targeting a glucose level of 80 to 110 mg per deciliter did not change the rate of healthcare–associated infections, mortality, or length of stay in the cardiac ICU as compared with standard care,” the researchers wrote.

They acknowledged that certain limitations of the trial should be considered, however, and that this group of pediatric patients is unique, so the results “cannot be extrapolated to other pediatric critical care populations.”

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