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MRSA Colonization and Infection
Methicillin-Resistant Staphylococcus aureus Colonization and Its Association with Infection among Infants Hospitalized in Neonatal Intensive Care Units. Huang Y-C, et al Pediatrics 2006; Aug: 118(2):469-474. [Full text] [PDF]
OBJECTIVE.
To assess the rate of methicillin-resistant Staphylococcus aureus
colonization and its association with infection among infants
hospitalized in methicillin-resistant S aureus–endemic NICUs.
METHODS. Between March 2003 and February 2004, surveillance
surface culture specimens were obtained weekly from multiple sites of
infants admitted to the NICUs at a children’s hospital in Taiwan for
the detection of methicillin-resistant S aureus. All colonized
and clinical isolates from each study infant with methicillin-resistant
S aureus infection were genotyped with pulsed-field gel
electrophoresis, with Sma1 digestion, and compared.
RESULTS.
A total of 783 infants were included in this study. Methicillin-resistant
S aureus colonization was detected for 323 infants during
their NICU stays, with detection with the first 2 samples for 89%.
Nares and umbilicus were the 2 most common sites of initial
colonization. Methicillin-resistant S aureus colonization was
associated significantly with premature birth (
28
weeks) and low birth weight (
1500
g), and infants with colonization had a significantly higher rate of
methicillin-resistant S aureus infection, compared with those
without colonization (26% vs. 2%). Methicillin-resistant S aureus
colonization was noted for 84 of 92 infants with methicillin-resistant
S aureus infections. Of the 68 episodes with previous
colonization and isolates available for genotyping analysis,
colonized and clinical isolates were indistinguishable in 63
episodes, highly related in 2 episodes, and distinct in 3 episodes.
CONCLUSIONS. More than 40% of the hospitalized infants were colonized with methicillin-resistant S aureus during their stay in methicillin-resistant S aureus–endemic NICUs; this was associated significantly with methicillin-resistant S aureus infection. Most infants with methicillin-resistant S aureus infections had previous colonization with an indistinguishable strain.
Commentary: With the rise in community colonization rates of MRSA (or ORSA, for oxacillin-resistant Staph aureus), this organism has now emerged as a vexing and morbid pathogen in the NICU. After a couple of index cases of severe systemic ORSA infection in one of our NICUs about 2 years ago, we instituted infection control procedures that included isolation of all outborn infants (until proven ORSA-negative), weekly surveillance cultures of all NICU patients with bactoban treatment and isolation of positive patients, and cohorting of nursing staff as best as we were able. We have consulted on multiple occasions with the CDC. The result: we have “controlled” but have not eradicated ORSA
(our colonization rate varies between 2.5 and 20%). Of note in this study is the approximate 25% risk of systemic infection among infants colonized with ORSA, with the risk greatest among the most vulnerable infants. Although the bloodstream infection is typically cleared rapidly with vancomycin, soft tissue and bone/joint infections are difficult to treat because vancomycin (in contrast to nafcillin) has relatively poor penetrance into those compartments. It is most unfortunate that prophylactic treatment with Veronate® (human IVIG with enhanced anti-staphylococcal activity) was shown so unambiguously to be ineffective. The prevalence and morbidity of this organism has worked against efforts not to employ vancomycin as a first-line therapy when nosocomial sepsis is suspected. Perhaps as a consequence, we have begun to see intermittent VRE (vancomycin-resistant Enterococcus) colonization in our infants. The bugs are smart. Will the era of antibiotics as wonder drugs be a short one hundred year footnote in history? - MLH
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