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Randomized Controlled Trial
. 2015 Jul 20;128(14):1922-31.
doi: 10.4103/0366-6999.160546.

Goal-directed Fluid Therapy May Improve Hemodynamic Stability of Parturient with Hypertensive Disorders of Pregnancy Under Combined Spinal Epidural Anesthesia for Cesarean Delivery and the Well-being of Newborns

Affiliations
Randomized Controlled Trial

Goal-directed Fluid Therapy May Improve Hemodynamic Stability of Parturient with Hypertensive Disorders of Pregnancy Under Combined Spinal Epidural Anesthesia for Cesarean Delivery and the Well-being of Newborns

Wei Xiao et al. Chin Med J (Engl). .

Abstract

Background: Hypotension induced by combined spinal epidural anesthesia in parturient with hypertensive disorders of pregnancy (HDP) can easily compromise blood supply to vital organs including uteroplacental perfusion and result in fetal distress. The aim of this study was to investigate whether the goal-directed fluid therapy (GDFT) with LiDCO rapid system can improve well-being of both HDP parturient and their babies.

Methods: Fifty-two stable HDP parturient scheduled for elective cesarean delivery were recruited. After loading with 10 ml/kg lactated Ringer's solution (LR), parturient were randomized to the GDFT and control group. In the GDFT group, individualized fluid therapy was guided by increase in stroke volume (ΔSV) provided via LiDCO rapid system. The control group received the routine fluid therapy. The primary endpoints included maternal hypotension and the doses of vasopressors administered prior to fetal delivery. The secondary endpoints included umbilical blood gas abnormalities and neonatal adverse events.

Results: The severity of HDP was similar between two groups. The total LR infusion (P < 0.01) and urine output (P < 0.05) were higher in the GDFT group than in the control group. Following twice fluid challenge tests, the systolic blood pressure, mean blood pressure, cardiac output and SV in the GDFT group were significantly higher, and the heart rate was lower than in the control group. The incidence of maternal hypotension and doses of phenylephrine used prior to fetal delivery were significantly higher in the control group than in the GDFT group (P < 0.01). There were no differences in the Apgar scores between two groups. In the control group, the mean values of pH in umbilical artery/vein were remarkably decreased (P < 0.05), and the incidences of neonatal hypercapnia and hypoxemia were statistically increased (P < 0.05) than in the GDFT group.

Conclusions: Dynamic responsiveness guided fluid therapy with the LiDCO rapid system may provide potential benefits to stable HDP parturient and their babies.

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Conflict of interest statement

Conflict of Interest: None declared.

Figures

Figure 1
Figure 1
Patients’ recruitment flow chart. Patients were excluded from our study for the following reasons: 1 for ASA physical level of III–V; 1 for twin pregnancy; 2 for contraindications for spinal anesthesia; 2 for known fetal abnormalities; 3 for known coexisting diseases except HDP; 6 for early-onset HDP, 2 for gestational weeks <37 weeks, 2 for unstable HDP, and 1 for refusing to participate. GDFT: Goal-directed fluid therapy; ASA: American Society of Anesthesiology; HDP: Hypertensive disorders of pregnancy.
Figure 2
Figure 2
Protocol for intraoperative management. LR: Lactated Ringer's solution; CSEA: Combined spinal epidural anesthesia; GDFT: Goal-directed fluid therapy; ΔSV: Increase in stroke volume; SV: Stroke volume; HR: Heart rate.
Figure 3
Figure 3
Mean differences in hemodynamic variables between the two groups. (a) Systolic blood pressure; (b) Mean blood pressure; (c) Heart rate; (d) Cardiac output; (e) Stroke volume were monitored at the following time points in both groups. T1: Baseline; T2: Following coloading with LR of 10 ml/kg; T3: 4 min following LR coloading (following first fluid challenge test); T4: 8 min following LR coloading (following second fluid challenge test); T5: Stable blockade level obtained (thoracic level 5–3); T6: Immediate after delivery; T7: Placental expulsion; T8: Discharge from operating room. Diamond with blue line and square with red line indicate the control group and the GDFT group at that time, respectively. Data were expressed as mean ± standard deviation; *Significantly different at P < 0.05 compared with the baseline (T1) in each group, †Significantly different at P < 0.05 compared between the two groups. GDFT: Goal-directed fluid therapy; LR: Lactated Ringer's solution.

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