Risk Factors for Early Infant Colonization With Methicillin-Resistant Staphylococcus Aureus
The prevalence of Methicillin-resistant Staphylococcus aureus (MRSA) colonization and infections have been increasing in the general population, including the pediatric population. It has been reported that MRSA colonization persists for up to four years, and therefore the youngest pediatric patients, specifically those who are less than 2 years of age, have a high risk of prolonged colonization during a period of time when they are susceptible to significant skin and soft tissue infections (SSTIs) attributable to MRSA. Once prolonged colonization takes place, recurrent SSTIs are commonplace, resulting in substantial morbidity and in some cases mortality, as well as a significant cost to the healthcare system. Individuals colonized with MRSA have an increased risk of developing MRSA infections, which range from mild disease, such as carbuncles, to severe infections, such as necrotizing pneumonia and toxic shock syndrome. The prevalence of severe MRSA infections is also greatest in neonates and infants, where increased MRSA colonization has been observed. In the early infant period, the most common manifestation of MRSA disease is pustular skin lesions, which affect approximately 5% of the general population, with MRSA-colonization being a major risk factor for this disease. Moreover, the prevalence of pustular disease is increasing in the general population, and there are numerous case reports of invasive, life-threatening MRSA disease in the early infant period.
Corresponding to the increasing prevalence in the community, the carriage of MRSA in pregnant women has also escalated, and vaginal carriage is significant in pregnant women. As an analogy, maternal vaginal Group B Streptococcal (GBS) colonization is the major risk for infant colonization regardless of whether early or late neonatal colonization or disease occurs. It is quite feasible that vaginal MRSA carriage predisposes newborns to colonization during the birthing process; however, this mechanism has not yet been well studied. There are other mechanisms implicated for early infant colonization, including close contact with MRSA-colonized mothers through daily care and breastfeeding. MRSA colonization in one household member greatly predisposes colonization in others; therefore, early infant colonization could result from contact with other MRSA-colonized individuals in a household. Currently, it is not clear which factors are the most important in influencing early infant MRSA colonization and subsequent infection.
Not only is the prevalence of MRSA colonization and infection on the rise, but there have been few if any measures that have been established to prevent colonization and subsequent infection in adults and children. Eradication measures have shown limited long-term benefit. If vertical transmission of MRSA can be established as a critical event in the pathogenesis of disease, potentially effective strategies could be tested, and possibly the spread of MRSA in the community interrupted.
Hypotheses and Specific Aims:
- Identify the proportion, rate and time of MRSA colonization in infants born to mothers with and without MRSA colonization;
- Compare risk factors for infant MRSA colonization in these two groups;
- Determine the prevalence and risk factors for developing MRSA infections in the MRSA-colonized infant.
Methicillin-resistant Staphylococcus Aureus
|Study Design:||Observational Model: Cohort
Time Perspective: Prospective
|Official Title:||Risk Factors for Early Infant Colonization With Methicillin-Resistant Staphylococcus Aureus|
- We will compare infants' MRSA-positivity rates in the exposed versus the unexposed study groups. [ Time Frame: 18 months ]
- We will determine if infant MRSA positivity appears earlier in exposed infants versus unexposed infants. [ Time Frame: 18 months ]
- For infants who become MRSA-positive we will determine if their strain of MRSA is the same as their mothers' or other household contacts or care giver who is determined to be MRSA-positive. [ Time Frame: 18 months ]
Biospecimen Retention: Samples Without DNA
|Study Start Date:||June 2010|
|Study Completion Date:||June 2012|
|Primary Completion Date:||June 2012 (Final data collection date for primary outcome measure)|
The MRSA-exposed group will include 100 MRSA-colonized mothers and their babies
The MRSA-unexposed group will include 100 MRSA-negative mothers and their babies.
Please refer to this study by its ClinicalTrials.gov identifier: NCT01141101
|United States, Massachusetts|
|Boston Medical Center|
|Boston, Massachusetts, United States, 02118|