Community-Acquired Methicillin Resistant Staphylococcus Aureus Colonization in Pregnant Women and Infections in Newborns
Primary Purpose
Staphylococcus Aureus Infection
Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
CA-MRSA Decolonization
Sponsored by
About this trial
This is an interventional prevention trial for Staphylococcus Aureus Infection focused on measuring Methicillin resistant Staphylococcus aureus, Staphylococcus aureus, Healthy term and near term neonates, Prevention, Nasal and Vaginal Colonization rates, Pregnant women
Eligibility Criteria
Inclusion Criteria:
- Healthy pregnant women who present for routine OB/GYN care during the of the 34-36 week gestation GBS screening visit.
- Healthy term and near-term infants born to these mothers
Exclusion Criteria:
- Pre-term infants
- Infants who had significant illness after birth, i.e. transferred to neonatal intensive care unit for significant illness.
Age limits for infants will be 0-4 weeks of age and both genders will be included.
Sites / Locations
- Prentice Women's Hospital and Maternity Center of Northwestern Memorial HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
No Intervention
Other
Arm Label
A
B
Arm Description
Pregnant women not receiving CA-MRSA decolonization therapy.
Pregnant women receiving CA-MRSA decolonization therapy.
Outcomes
Primary Outcome Measures
CA-MRSA vaginal and nasal colonization rates in pregnant women at the time of routine Group B Streptococcus (GBS) Screening at 34-36 week gestation visit.
The incidence of CA-MRSA skin, soft tissue and invasive (SSTI) infections in healthy term and near-term infants born to CA-MRSA colonized mothers.
Secondary Outcome Measures
In later stages of the study, we will study the efficacy of attempted decolonization in CA-MRSA colonized mothers in decreasing the incidence of transmission and development of SSTI and invasive infections in their infants during the first month of life.
Full Information
NCT ID
NCT00532324
First Posted
September 19, 2007
Last Updated
March 10, 2011
Sponsor
Ann & Robert H Lurie Children's Hospital of Chicago
Collaborators
Thrasher Research Fund, Northwestern Memorial Hospital
1. Study Identification
Unique Protocol Identification Number
NCT00532324
Brief Title
Community-Acquired Methicillin Resistant Staphylococcus Aureus Colonization in Pregnant Women and Infections in Newborns
Official Title
Community-Acquired Methicillin Resistant Staphylococcus Aureus (CA-MRSA) Vaginal and Nasal Colonization in Pregnant Women and Frequency of CA-MRSA Infections in Previously Healthy Term and Near-Term Neonates
Study Type
Interventional
2. Study Status
Record Verification Date
April 2009
Overall Recruitment Status
Unknown status
Study Start Date
January 2008 (undefined)
Primary Completion Date
December 2009 (Anticipated)
Study Completion Date
January 2010 (Anticipated)
3. Sponsor/Collaborators
Name of the Sponsor
Ann & Robert H Lurie Children's Hospital of Chicago
Collaborators
Thrasher Research Fund, Northwestern Memorial Hospital
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Background:
Community acquired methicillin-resistant Staphylococcus aureus (CA-MRSA) is an emerging pathogen of the 21st century whose incidence as a cause of local and invasive infections has significantly increased, especially in previously healthy term and near term newborns. The etiology of the increasing incidence of infection in previously healthy term and near-term newborns remains unclear.
Hypothesis:
The incidence of previously healthy newborns infected with CA-MRSA skin & soft tissue (SSTI) and invasive infections is higher in those born to mothers colonized with CA-MRSA.
Pregnant women colonized with CA-MRSA are at higher risk for post-partum infection with this organism.
Specific Aims:
To determine the incidence of nasal and vaginal colonization with CA-MRSA in pregnant women and determine the genetic similarities of these strains.
To study CA-MRSA transmission dynamics and evaluate the incidence of SSTI and invasive infections in newborns born to S. aureus colonized mothers.
To study the efficacy of attempted decolonization in CA-MRSA colonized mothers in decreasing the incidence of transmission and development of SSTI and invasive infections in their infants during the first month of life.
Potential Impact:
Understanding the epidemiology of the transmission dynamics of CA-MRSA in previously healthy newborns will provide important information to support the development of strategies aimed at the interruption of transmission and prevention of infection caused by CA-MRSA in newborns, as well as in pregnant women. This will also allow for the development of infection control strategies to prevent the spread of this organism among post-partum units and nurseries.
Detailed Description
Background:
Community acquired methicillin-resistant Staphylococcus aureus (CA-MRSA) is an emerging pathogen of the 21st century whose incidence as a cause of local and invasive infections has significantly increased, especially in previously healthy term and near term neonates where it may be associated with high morbidity and mortality(1, 2, 3). The etiology for this increase remains unclear, but may be a consequence of perinatal or postnatal acquisition via maternal transmission through skin, breast milk, or vaginal colonization(4).
The major goals of our study are: to determine the incidence of pregnant women who are colonized with CA-MRSA, gain a better understanding of the transmission dynamics of this organism between the mother and the newborn infant, and to develop strategies for the prevention of transmission, spread and infection with this organism in both these populations.
This staged study is a collaborative effort between investigators from the Children's Memorial Hospital Division of Infectious Diseases, Northwestern Memorial Hospital Department of Obstetrics and Gynecology, and the Northwestern Memorial Hospital Division of Infectious Diseases. Collaboration across multiple specialties provides strength to the study by allowing the investigators to address multiple issues that are pertinent to both the care of pregnant mothers and newborn infants in the inpatient and outpatient setting.
Hypothesis:
1. The incidence of previously healthy term and near-term neonates infected with CA-MRSA skin & soft tissue (SSTI) and invasive infections is higher in those born to mothers vaginally and/or nasally colonized with CA-MRSA and, 2. Pregnant women vaginally and/or nasally colonized with CA-MRSA are at higher risk for post-partum infection with this organism.
Specific Aims:
To determine the incidence of nasal and vaginal colonization with CA-MRSA in pregnant women and determine the clonality of these strains.
To study CA-MRSA transmission dynamics and evaluate the incidence of SSTI and invasive infections in term and near-term newborns born to S. aureus vaginal and/or nasal colonized mothers.
To study the efficacy of attempted decolonization in CA-MRSA colonized mothers in decreasing the incidence of transmission and development of SSTI and invasive infections in their infants during the first month of life.
Methods:
Vaginal and anterior nasal cultures will be obtained prospectively over several months from pregnant women who obtain their prenatal care through Obstetrical practices at Prentice Women's Hospital and Maternity Center of Northwestern Memorial Hospital during the time of GBS screening at 34-36 weeks gestation. Together, these practices account for 300-500 deliveries per month.
Cultures will be plated on blood agar and incubated at 37oC for 48 hours. S. aureus strains will be identified by colony morphology and latex agglutination. MRSA isolates will be identified by PCR or latex agglutination for penicillin binding protein 2a by detecting the mecA gene and clonality by PFGE. PCR testing will then be used to identify strains carrying the Panton-Valentine Leukocidin gene as a marker of virulence.
In a prospective case-control cohort study, newborns born to CA-MRSA colonized mothers will have anterior nares cultures for S. aureus obtained at birth and followed for the development of SSTI and invasive infections for one month. Samples positive for MRSA will be tested for similarities to maternal isolates through methods described above. The newborn incidence of MRSA infection will be compared between those born to non-colonized mothers and those born to colonized mothers.
In further stages of this study, women found to be nasally and/or vaginally colonized with CA-MRSA will be randomized to receive postpartum, either: 1) attempted decolonization with intranasal mupirocin with or without diluted chlorhexidine or Clorox baths or, 2) no intervention.
Potential Impact:
Understanding the epidemiology of the transmission dynamics of CA-MRSA in previously healthy neonates will provide important information to support the development of strategies aimed at the interruption of transmission and prevention of infection caused by CA-MRSA in this patient population, as well as in pregnant women. This will also allow for the development of infection control strategies in the hospital setting to prevent the spread of this organism among post-partum units and nurseries.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Staphylococcus Aureus Infection
Keywords
Methicillin resistant Staphylococcus aureus, Staphylococcus aureus, Healthy term and near term neonates, Prevention, Nasal and Vaginal Colonization rates, Pregnant women
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
1500 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
A
Arm Type
No Intervention
Arm Description
Pregnant women not receiving CA-MRSA decolonization therapy.
Arm Title
B
Arm Type
Other
Arm Description
Pregnant women receiving CA-MRSA decolonization therapy.
Intervention Type
Other
Intervention Name(s)
CA-MRSA Decolonization
Other Intervention Name(s)
Mupirocin also known as Bactroban, Chlorhexidine also known as Phisohex, Clorox
Intervention Description
In later stages of this study, women found to be nasally and/or vaginally colonized with CA-MRSA will be randomized to receive postpartum, either: 1) attempted decolonization with intranasal mupirocin twice a day for one to two weeks with or without diluted chlorhexidine or Clorox baths two to three times a week for one to two weeks or, 2) no intervention. The primary study is observational only.
Primary Outcome Measure Information:
Title
CA-MRSA vaginal and nasal colonization rates in pregnant women at the time of routine Group B Streptococcus (GBS) Screening at 34-36 week gestation visit.
Time Frame
We will obtain vaginal and nasal samples at the 34-36 week gestation OB/Gyn visit.
Title
The incidence of CA-MRSA skin, soft tissue and invasive (SSTI) infections in healthy term and near-term infants born to CA-MRSA colonized mothers.
Time Frame
Infants born to CA-MRSA colonized mothers will be followed for CA-MRSA colonization and/or SSTIs for the first 4 weeks of life.
Secondary Outcome Measure Information:
Title
In later stages of the study, we will study the efficacy of attempted decolonization in CA-MRSA colonized mothers in decreasing the incidence of transmission and development of SSTI and invasive infections in their infants during the first month of life.
Time Frame
Infants born to CA-MRSA colonized moms will be followed for CA-MRSA colonization and/or SSTIs for the first 4 weeks of life.
10. Eligibility
Sex
Female
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Healthy pregnant women who present for routine OB/GYN care during the of the 34-36 week gestation GBS screening visit.
Healthy term and near-term infants born to these mothers
Exclusion Criteria:
Pre-term infants
Infants who had significant illness after birth, i.e. transferred to neonatal intensive care unit for significant illness.
Age limits for infants will be 0-4 weeks of age and both genders will be included.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Tina Q Tan, M.D.
Phone
773-880-4187
Email
titan@childrensmemorial.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tina Q Tan, M.D.
Organizational Affiliation
Children's Memorial Hospital/Northwestern University Feinberg School of Medicine
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Latania K Logan, M.D.
Organizational Affiliation
Children's Memorial Hospital/Northwestern University Feinberg School of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Prentice Women's Hospital and Maternity Center of Northwestern Memorial Hospital
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60611
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Tina Q Tan, M.D.
Phone
773-880-4187
Email
titan@childrensmemorial.org
First Name & Middle Initial & Last Name & Degree
Tina Q Tan, M.D.
First Name & Middle Initial & Last Name & Degree
Ami Patel, B.S.
First Name & Middle Initial & Last Name & Degree
Alan Peaceman
First Name & Middle Initial & Last Name & Degree
Latania K Logan, M.D.
12. IPD Sharing Statement
Citations:
PubMed Identifier
16514341
Citation
Kollef MH, Micek ST. Methicillin-resistant Staphylococcus aureus: a new community-acquired pathogen? Curr Opin Infect Dis. 2006 Apr;19(2):161-8. doi: 10.1097/01.qco.0000216627.13445.e2.
Results Reference
background
PubMed Identifier
15876949
Citation
Crawford SE, Daum RS. Epidemic community-associated methicillin-resistant Staphylococcus aureus: modern times for an ancient pathogen. Pediatr Infect Dis J. 2005 May;24(5):459-60. doi: 10.1097/01.inf.0000164170.67897.97. No abstract available.
Results Reference
background
PubMed Identifier
15712079
Citation
Deresinski S. Methicillin-resistant Staphylococcus aureus: an evolutionary, epidemiologic, and therapeutic odyssey. Clin Infect Dis. 2005 Feb 15;40(4):562-73. doi: 10.1086/427701. Epub 2005 Jan 24.
Results Reference
background
PubMed Identifier
16950976
Citation
Fortunov RM, Hulten KG, Hammerman WA, Mason EO Jr, Kaplan SL. Community-acquired Staphylococcus aureus infections in term and near-term previously healthy neonates. Pediatrics. 2006 Sep;118(3):874-81. doi: 10.1542/peds.2006-0884.
Results Reference
background
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Community-Acquired Methicillin Resistant Staphylococcus Aureus Colonization in Pregnant Women and Infections in Newborns
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