Topical Mupirocin highly effective in Staph infections in NICU babies

In this study, between 10 and 45 percent of infants became colonized with SA in the eight NICUs across the country that participated in this study. A 5-day course of mupirocin was applied to the skin and nasal passages of the infants in the NICU who tested positive for SA. The results indicate mupirocin is safe and highly effective in eliminating SA from the skin and nasal passages of these infants. More than 90 percent of the treated infants tested negative for SA after treatment, indicating effective "decolonization" in response to mupirocin. This is the first randomized multicenter clinical trial to demonstrate the effectiveness and safety of mupirocin in infants, including those born prematurely, and to show that this treatment reduced colonization by both SA that are susceptible to commonly used antibiotics (MSSA) and those that are not (MRSA).

SA are bacteria that are commonly present on the skin and mucous membranes without causing disease. When bacteria live in the body without causing disease, this is referred to as colonization. Infants who become colonized with SA while hospitalized are at increased risk of developing life-threatening infections. Therefore, this treatment is likely to reduce clinical infection in infants. The effect of a course of mupirocin lasted for at least two to three weeks.

About the Research

This study performed a randomized clinical trial with premature and full-term newborns and children under two years old who were admitted to the NICU for stays of at least 14 days. The study did not include a placebo control, because even the application of ointments without any active ingredients into the nose of premature infants has been associated with infection. There were two goals of the study: (i) to determine if applying mupirocin to the nasal passages, perianal region, and the umbilical region was safe and well tolerated; (ii) to determine if topically applied mupirocin eliminated SA in infants that tested positive in a nasal swab for the presence of SA.

Of the more than 6,000 babies admitted to the NICU and tested for SA by nasal swab, 18 percent were positive. The randomized study evaluated 155 of the 1,140 infants who tested positive. Rash in the perianal region, usually attributed to other causes, was the most common adverse reaction in treated infants. There was no evidence that the treatment resulted in unintended disease that could result from perturbations of the gastrointestinal microbiome. Thus, the topically applied mupirocin was well tolerated and safe.

More than 90 per cent of the treated infants tested negatively for SA after treatment, indicating effective "decolonization" in response to mupirocin. For the infants who remained in the NICU and were tested at three weeks, approximately 50 percent of the treated infants and only two percent of the untreated infants remained negative for SA. Encouragingly, there was no evidence of the emergence of methicillin-resistant strains. Thus, this is the first randomized multicenter clinical trial to demonstrate the effectiveness and safety of mupirocin in infants, including those born prematurely, and to show that this treatment reduced colonization by both SA that are susceptible to commonly used antibiotics (MSSA) and those that are not (MRSA). Because the incidence of clinical infection was low, the study cannot show with statistical confidence that the five-day mupirocin treatment prevented clinical SA infection. However, this outcome can be inferred from reduction in colonization by the bacteria. Furthermore, the finding that many babies became recolonized indicates that other strategies are needed to manage infection in babies requiring long-term hospitalization. Despite these limitations, the study provides strong support for using mupirocin to limit the risk of SA infection in the NICU.

"Improving infant survival and limiting risks associated with hospital admissions is an ongoing goal at UMSOM. This multicenter trial supervised by Dr. Kotloff provides strong support for a safe strategy to minimize Staphylococcus aureus infections in some of the most at-risk patients in any hospital, premature babies," said UMSOM Dean E. Albert Reece, MD, PhD, MBA, who is also the Executive Vice President for Medical Affairs, University of Maryland, and the John Z. and Akiko K. Bowers Distinguished Professor.