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The Effects of Varying Volumes of Crystalloid Administration Before Cesarean Delivery on Maternal Hemodynamics and Colloid Osmotic Pressure

Grace E. ParkDepartment of Anesthesia, Harvard Medical School, Brigham and Women's Hospital, Boston, Massachusetts 02115, USAMartha A. HauchDepartment of Anesthesia, Harvard Medical School, Brigham and Women's Hospital, Boston, MassachusettsFred CurlinDepartment of Anesthesia, Harvard Medical School, Brigham and Women's Hospital, Boston, MassachusettsSanjay DattaDepartment of Anesthesia, Harvard Medical School, Brigham and Women's Hospital, Boston, MassachusettsAngela M. BaderDepartment of Anesthesia, Harvard Medical School, Brigham and Women's Hospital, Boston, Massachusetts
1996en
ABI

Аннотация

The value of intravenous crystalloid administration in preventing spinal-induced hypotension in the parturient has recently been questioned. Also, the association between increasing crystalloid volume and decreasing postpartum colloid osmotic pressure (COP) raises concern regarding the risk of maternal and fetal pulmonary edema. To study the dose-response effect of varying amounts of crystalloid volume prior to spinal anesthesia, we measured maternal hemodynamic variables and maternal and fetal COP in three groups of healthy parturients receiving spinal anesthesia for elective cesarean delivery. Fifty-five parturients were randomized in a double-blind fashion to receive one of 10, 20, or 30 mL/kg of crystalloid volumes prior to induction of spinal anesthesia. Measurements included mean arterial blood pressure (MAP), cardiac index (CI), and systemic vascular resistance index (SVRI) recorded using noninvasive thoracic impedance monitoring until delivery. Maternal and neonatal COP were measured. All groups showed declines in MAP and SVRI from baseline at 5 min after spinal anesthesia, but the amount of decline did not differ among groups. Total ephedrine and additional intravenous (i.v.) fluid administered did not differ among groups. The 20- and 30- mL/kg groups showed a larger decline in maternal COP than the 10-mL/kg group; no differences in neonatal COP were seen with varying preload. We conclude that increasing the amount of i.v. crystalloid administered to 30 mL/kg in the healthy parturient does not significantly alter maternal hemodynamics or ephedrine requirements after spinal anesthesia and has no apparent benefit.

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