PEDIATRICS Vol. 102 No. 5 November 1998, pp. 1107-1111
Preliminary Report: rhG-CSF May Reduce the Incidence of Neonatal Sepsis in Prolonged Preeclampsia-associated Neutropenia
Received Feb 6, 1998; accepted May 4, 1998.
From the Departments of Pediatrics and Neurobiology, State University at Stony Brook, Stony Brook, New York.
Objectives. To determine whether
adjunctive therapy with recombinant human granulocyte
colony-stimulating factor (rhG-CSF) could reverse the neutropenia and
reduce the incidence of sepsis (
28 days postnatal age) in neonates
with prolonged preeclampsia-associated neutropenia compared with
conventional therapy.
Study Design. An intravenous infusion of rhG-CSF (10 µg/kg/day × 3 days for 10 neonates or 5 µg/kg/day × 3 days for 5 neonates) was administered to ventilated patients with
prolonged (
3 consecutive days in the first postnatal week)
preeclampsia-associated neutropenia (absolute neutrophil count [ANC]
<1500/mm3). Neutrophilic responses and the incidence of
neonatal sepsis in the next 28 postnatal days were compared with 13 case-matched control neonates who also had prolonged
preeclampsia-associated neutropenia. Sepsis was defined as at least one
positive blood culture in a newly symptomatic neonate treated with
antibiotics for
7 days.
Results. No significant differences existed among the
three groups in the birth weight, gestational age, sex, growth
retardation, method of delivery, magnitude of respiratory support, use
of surfactant, usage of intravascular catheters, or in the initial
(pretreatment) ANC. The average baseline ANC (pretreatment) in the
10-µg rhG-CSF group was 815 ± 169/mm3 (mean ± SEM), in the 5 µg group it was 786 ± 165/mm3, and
in the conventional group it was 965 ± 283. Eighteen of 28 (64%)
neonates with preeclampsia-associated neutropenia were neutropenic at
birth, the other 10 (36%) had normal neutrophil counts at birth but
subsequently developed
3 days of neutropenia between 24 and 120 hours
after birth. The ANC increased by 2-fold at 24 hours, by 4-fold at 72 hours, and 14-fold by the 7th day in the 10-µg group. In the 5-µg
group, a 2-fold and 5-fold increase occurred at 72 hours and 7 days,
respectively. In the conventionally-treated group, only a 4-fold
increase was seen as late as 7 days after achieving entry criteria.
Sepsis was observed in 13% (2/15) of the rhG-CSF-treated neonates
compared with an incidence of 54% (7/13) in the conventionally-treated
neonates.
Conclusions. rhG-CSF increases the ANC significantly (at 10 µg/kg/day × 3 days) and reduces the incidence of neonatal sepsis in critically ill ventilated neonates with prolonged preeclampsia-associated neutropenia when compared with conventional therapy. A future prospective, randomized, and blinded trial is needed to validate the beneficial effects of prophylactic rhG-CSF therapy in neonates with prolonged preeclampsia-associated neutropenia. Key words: neonatal sepsis, granulocyte colony stimulating factor (rhG-CSF), bacteremia, cytokines, very low birth weight, neutropenia, preeclampsia.
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