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Licensed Unlicensed Requires Authentication Published by De Gruyter February 21, 2019

Erythropoietin in perinatal hypoxic-ischemic encephalopathy: a systematic review and meta-analysis

  • Abdul Razak ORCID logo EMAIL logo and Asif Hussain

Abstract

Background

Erythropoietin (EPO) appears to confer neuroprotection to the injured brain. Randomized clinical trials (RCTs) have demonstrated its safety in neonates with hypoxic-ischemic encephalopathy (HIE); however, the evidence is unclear. The objective of this study was to examine the role of EPO in perinatal HIE by a systematic review and meta-analysis.

Methods

Database search included Embase, MEDLINE, Cumulative Index to Nursing and Allied Health Literature (CINAHL) and Cochrane Central Register of Controlled Trials (CENTRAL). RCTs reporting a death, neurodevelopmental outcomes or brain injury were included. Two authors extracted the data independently from included studies and assessed the level of evidence (LOE).

Results

Six RCTs (EPO=5 and darbepoetin α=1) involving 454 neonates were included. A trend toward a lower risk of death was identified in infants treated with EPO [EPO with or without hypothermia: five RCTs, 368 participants, relative risk (RR) 0.74, 95% confidence interval (CI) 0.47–1.19, LOE−low; EPO without hypothermia: four RCTs, 318 participants, RR 0.89, 95% CI 0.49–1.32, LOE−low]. EPO treatment without hypothermia compared to placebo resulted in a reduced risk of cerebral palsy (two RCTs, 230 participants, RR 0.47, 95% CI 0.27–0.80, LOE−moderate) and moderate to severe cognitive impairment (two RCTs, 226 participants, RR 0.49, 95% CI 0.28–0.85, LOE−moderate). A reduced risk of brain injury was identified in EPO treated infants (EPO with or without hypothermia, two RCTs, 148 participants, RR 0.70, 95% CI 0.53–0.92, LOE−moderate).

Conclusion

EPO administration in neonates with perinatal HIE reduces the risk of brain injury, cerebral palsy and cognitive impairment. The evidence is limited to suggest its role as an adjuvant to hypothermia. Larger powered trials are underway to overcome this limitation.


Corresponding author: Dr. Abdul Razak, MD, Associate Clinical Professor, Staff Neonatologist, Division of Neonatology, Department of Pediatrics, Princess Nourah Bint AbdulRahman University, King Abdullah bin Abdul Aziz University Hospital, Riyadh 13412, Saudi Arabia; and Department of Pediatrics, McMaster University, Hamilton, ON, L8S 4L8, Canada, Tel.: +966560636849, E-mail:

  1. Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.

  2. Research funding: None declared.

  3. Employment or leadership: None declared.

  4. Honorarium: None declared.

  5. Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.

  6. Registration: PROSPERO, registration number CRD42018085799, the international prospective register for systematic reviews (https://www.crd.york.ac.uk/PROSPERO).

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Supplementary Material

The online version of this article offers supplementary material (https://doi.org/10.1515/jpm-2018-0360).


Received: 2018-10-27
Accepted: 2019-01-28
Published Online: 2019-02-21
Published in Print: 2019-05-27

©2019 Walter de Gruyter GmbH, Berlin/Boston

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