NeoNotes
Journal Club
Andrew B. Kairalla MD, Editor
10-038 | Additional Comments |
Previous
Article | Next Article | Search
| List of Articles | Submit
Comments | Index | FSN Home Page | Subscribe
Now
EPO may Improve Development
Brown MS, MD, Eichorst D,
LaLa-Black B, et al. Higher Cumulative Doses of Erythropoietin and
Developmental Outcomes in Preterm Infants. Pediatrics (October 2009);
124:e681-e687.
[Full
text]
[PDF]
OBJECTIVE:
We hypothesized that higher cumulative doses of recombinant
erythropoietin (rEPO) for extremely preterm infants during the first
6 postnatal weeks would improve developmental outcomes, as evidenced
in evaluations with the Bayley Scales of Infant Development-II
Revised.
METHODS: This was a retrospective cohort study with a data set
for a group (N = 366) of infants of <1500 g and
30
weeks of gestation that was created initially to examine the
association between rEPO treatment and retinopathy of prematurity.
Infants who underwent developmental follow-up evaluations at
corrected age of >12 months were included. The associations between
rEPO doses and higher Bayley Scales of Infant Development Psychomotor
Developmental Index and Mental Developmental Index (MDI) scores
were estimated in multivariate linear regression analyses.
RESULTS: Eighty-two infants underwent developmental evaluations
after 12 months. The median age of evaluation was 25 months.
The median 6-week cumulative rEPO dose was 3750 U/kg. In multivariate
analyses, Psychomotor Developmental Index (PDI) scores were
associated with transfusions, female gender, birth weight, and
5-minute Apgar scores (R2 = 0.39). MDI scores were associated
with 6-week rEPO dose, female gender, prenatal steroid treatment
for
48
hours, and breast milk feedings (R2 = 0.40).
CONCLUSIONS: These findings identify a dose-response relationship
between rEPO treatment and improved MDI scores. They are consistent
with findings of adult studies and animal brain injury models
and await confirmation.
Comments. It appears that erythropoietin is much more than an erythropoietic cytokine. It is produced locally in the nervous system, and is neurotrophic and neuroprotective in adult and neonatal animal models of brain injury. We now have evidence of a dose-response relationship between rEPO treatment and Bailey MDI scores. If these results are confirmed, I will need to rethink the value of early rEPO treatment in VLBW treatment. ABK
To comment on this article, Select Submit Comments.