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The role of fetal hemoglobin in the artificial placenta: A premature ovine model.

Authors :
Spencer BL
Fallon BP
McLeod JS
Cornell M
Perrone EE
Manthei DM
Rojas-Peña A
Hirschl RB
Bartlett RH
Mychaliska GB
Source :
Perfusion [Perfusion] 2024 Mar 22, pp. 2676591241240725. Date of Electronic Publication: 2024 Mar 22.
Publication Year :
2024
Publisher :
Ahead of Print

Abstract

Introduction: A radical paradigm shift in the treatment of premature infants failing conventional treatment is to recreate fetal physiology using an extracorporeal Artificial Placenta (AP). The aim of this study is to evaluate the effects of changing fetal hemoglobin percent (HbF%) on physiology and circuit function during AP support in an ovine model.<br />Methods: Extremely premature lambs ( n = 5) were delivered by cesarean section at 117-121 d estimated gestational age (EGA) (term = 145d), weighing 2.5 ± 0.35 kg. Lambs were cannulated using 10-14Fr cannulae for drainage via the right jugular vein and reinfusion via the umbilical vein. Lambs were intubated and lungs were filled with perfluorodecalin to a meniscus with a pressure of 5-8 cm H <subscript>2</subscript> O. The first option for transfusion was fetal whole blood from twins followed by maternal red blood cells. Arterial blood gases were used to titrate AP support to maintain fetal blood gas values.<br />Results: The mean survival time on circuit was 119.6 ± 39.5 h. Hemodynamic parameters and lactate were stable throughout. As more adult blood transfusions were given to maintain hemoglobin at 10 mg/dL, the HbF% declined, reaching 40% by post operative day 7. The HbF% was inversely proportional to flow rates as higher flows were required to maintain adequate oxygen saturation and perfusion.<br />Conclusions: Transfusion of adult blood led to decreased fetal hemoglobin concentration during AP support. The HbF% was inversely proportional to flow rates. Future directions include strategies to decrease the priming volume and establishing a fetal blood bank to have blood rich in HbF.<br />Competing Interests: Declaration of conflicting interestsThe author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Details

Language :
English
ISSN :
1477-111X
Database :
MEDLINE
Journal :
Perfusion
Publication Type :
Academic Journal
Accession number :
38519444
Full Text :
https://doi.org/10.1177/02676591241240725