GROUP B STREPTOCOCCUS
Group B
streptococcus (GBS) (orStreptococcus agalac-tiae) is an important cause of perinatal
infections. Asymptomatic lower genital tract colonization occurs in up to 30% of
pregnant women, but cultures may be posi-tive only intermittently, even in the
same patient. Approximately 50% of infants exposed to the organism in the lower
genital tract will become colonized. For most of these infants, such
colonization is of no consequence, but without treatment, GBS sepsis occurs in
approximately 0.2 infants per 1000 live births annually.
There are two manifestations of
clinical infection of the newborn, termed early-onset and late-onset,
occur-ring at roughly equal frequency. Early-onset
infection manifests as septicemia and septic shock, pneumonia, or meningitis
and occurs during the first week of life. Early-onset infection is much more
common in preterm infants than in term infants. Late-onset infection occurs later, after delivery, and has been
reported beyond 3 months (late-late onset
infection) in very low–birth-weight pre-term neonates. GBS disease in
newborns may occur as a result of vertical transmission or nosocomial or
community-acquired infection.
With prevention strategies,
current rates of early-onset GBS disease of the newborn have decreased to
approxi-mately 0.3 per 1000 live births. Currently, the Centers for Disease
Control and Prevention (CDC) and the American College of Obstetricians and
Gynecologists (ACOG) rec-ommend universal screening for GBS between 35 to 37
weeks of gestation.
All women
who are GBS positive by rectovaginal culture should receive antibiotic
prophylaxis in labor or with rupture of membranes.
If a patient’s culture status is
unknown, then prophylaxis should be given if any of the following conditions
exists:
· Preterm
labor (less than 37 weeks of gestation)
·
Preterm premature rupture of
membranes (PROM) (less than 37 weeks of gestation)
·
Rupture of membranes 18 hours or
longer
·
Maternal fever during labor (at
or above 38°C [100.4°F])
Women with GBS bacteriuria during
their current preg-nancy, or women who have previously given birth to an infant
with early-onset GBS disease also are candidates for intrapartum antibiotic
prophylaxis. When culture results are not available, intrapartum prophylaxis
should be of-fered only on the basis of the presence of intrapartum risk
factors for early-onset GMS disease. CDC Guidelines include recommended
medication regimens.
In the mother, significant
postpartum fever may indi-cate postpartum endometritis, sepsis, and, rarely,
meningi-tis, which may be caused by infection with GBS. With endometritis, the
onset is often sudden and within 24 hours of delivery. Significant fever and
tachycardia are typically present; sepsis may follow.
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