The primary outcome was to determine the incidence of GIB, with secondary outcomes including, comparing GIB incidence, adverse drug events commonly associated with SUP, and clinical outcomes between participants who did and did not receive SUP.
According to the abstract, a P value less than 0.05 was considered significant.
There were 233 patients included in the study. Twenty-two (9.4%) had GIB that occurred after a median (IQR) of 6 days of hydrocortisone. Another 54 participants (23.2%) received SUP, and histamine-2-receptor antagonists were used in 52 (96.3%) of these patients.
No significant difference in the rate of GIB was observed between patients with (n = 6 [11.1%]) and without SUP (n = 16 [8.9%]) (P = 0.632).
There were no significant differences for SUP-associated adverse effects between those who did and did not receive SUP, including for, “bacteremia (n = 12; 22.2% versus n = 43;25.7%, P = 0.605), urinary tract infection (n = 12; 22.2% versus n = 43; 24.0%, P = 0.785), meningitis (n = 1; 1.9% versus n = 4; 2.2%, P = 1.00), VAP (n = 6; 11.1% versus n = 25; 14.0%, P = 0.588), NEC (n = 6; 11.1% versus n = 21; 11.7%, P =0.901), or thrombocytopenia (n = 7; 13.0% versus n = 20; 11.2%, P =0.452),” respectively, according to results.
According to the study, it was concluded that SUP did not appear to provide prevention benefit for GIB and did not “pose an increase in SUP-associated adverse effects.”
Reference:
Miller JL, Farmer C, Ropp D, Stephens K, Johnson P. Incidence of gastrointestinal bleeding with hydrocortisone in neonates and infants less than three months of age in the neonatal intensive care unit. Abstract. Presented at: Health-System Pharmacists Midyear Clinical Meeting & Exhibition held in Anaheim, California. December 3, 2023, to December 7, 2023.