Left Ventricular Hemodynamic Effects of Rapid, in Utero Intravascular Transfusion in Anemic Fetal Lambs

We investigated the acute hemodynamic effects of in utero fetal intravascular transfusion in anemic fetuses. A conductance catheter technique of measuring left ventricular (LV) volume and pressure-volume analysis was employed in six anemic ovine fetuses of 131 days gestation (range 131-133 days). Th...

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Veröffentlicht in:The Journal of maternal-fetal medicine 1998, Vol.7 (1), p.51-58
Hauptverfasser: Kilby, Mark D., Szwarc, Richard S., Benson, Lee N., Morrow, Robert J.
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Sprache:eng
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Zusammenfassung:We investigated the acute hemodynamic effects of in utero fetal intravascular transfusion in anemic fetuses. A conductance catheter technique of measuring left ventricular (LV) volume and pressure-volume analysis was employed in six anemic ovine fetuses of 131 days gestation (range 131-133 days). The mean fetal weight at necropsy was 3,795 ± 166g. An intravascular transfusion of 120 ml packed maternal red cells was given over 12 minutes (rate of 2.6 ± 0.1 ml/kg/min) increasing the hematocrit from 22.5 ± 1.3% to 41.8 ± 0.8%. The infusion of packed red cells leads to an approximate increase in blood volume of 30%. Heart rate, left ventricular stroke volume, and contractility, as assessed by end-systolic elastance, did not change significantly with transfusion. Left ventricular afterload, as assessed by effective arterial elastance, increased from 11.4 ± 1.4 to 18.6 ± 2.8 (P < 0.01) mmHg/ml with transfusion, returning to baseline levels by 60 minutes posttransfusion. During the transfusion, end-diastolic pressure increased from 4.1 ± 0.4 to 10.6 ± 0.8 (P < 0.01) mmHg and end-diastolic volume increased from 2.0 ± 0.3 to 2.9 ± 0.5 ml/kg. However, by 60 minutes posttransfusion, end-diastolic pressure had returned to baseline levels, whereas end-diastolic volume remained elevated at 3.2 ± 0.6 ml/kg. We conclude that the persistent increase in end-diastolic volume implies a possible increase in LV diastolic compliance.
ISSN:1476-7058
1057-0802
1476-4954
DOI:10.3109/14767059809022654