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Rapid Intravenous Infusion of Mannitol Results in a Dipper-type Change in Stroke Volume Variation in Patients Undergoing Major Neurosurgery

Conditions
Craniotomy
Registration Number
NCT02237716
Lead Sponsor
First Affiliated Hospital, Sun Yat-Sen University
Brief Summary

The purpose of this study is to observe the variation of Hemodynamics、lactic acid、base excess、peripheral vascular resistance and DO2 through FloTrac™/Vigileo™ system after rapid infusion mannitol in neurosurgery.The hemodynamic changes after mannitol infusion are shown in Figure 1. HR (Fig. 1A) and systolic BP (Figure 1B) significantly increased between 0 min and 10 min (P = 0.041) and between -10 min and 10 min (P = 0.073), respectively; these two variables decreased steadily and returned to the baseline. Diastolic BP (Fig. 1B) showed no significant change after mannitol infusion (P = 0.102). CVP (Fig. 1C) significantly increased between -20 min and 0 min (P \< 0.001) and constantly decreased after 0 min, which remained below the baseline between 30 min and 60 min. CI (Fig. 1D) and SVI (Fig. 1E) showed a significant persistent increase between -20 min to 0 min (P \< 0.001) and between -20 min and 10 min (P \< 0.001), respectively. SVV exhibited a dipper-type change shown as a significant decrease between -20 min and 0 min and a significant increase between 0 min and 60 min (P \< 0.001), which returned to the baseline after 20 min.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
90
Inclusion Criteria
  • The inclusion criteria were: being aged between 16 and 70 years;
  • with a body mass index of 18-25 kg/m2;
  • with a physical status classified as ASA class I or II;
  • and scheduled for elective craniotomy
Exclusion Criteria
  • Any patient would be excluded from this study if the patient had complicating serious coagulopathy, hepatorenal insufficiency, aortic regurgitation, or cardiac arrhythmia;
  • had a previous history of intra-aortic balloon counterpulsation;
  • exhibited systolic blood pressure (SBP) ≥160 mmHg, diastolic blood pressure (DBP) ≥100 mmHg, or heart rate ≥ 100 bpm on operating room admission;
  • or rejected to participate in this study.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
stroke volume variationduring the procedure
peripheral vascular resistanceduring the procedure
cardiac indexduring the procedure
systolic pressureduring the procedure
central venous pressureduring the procedure
heart rateduring the procedure
stroke volume indexduring the procedure
Secondary Outcome Measures
NameTimeMethod
base excessduring the procedure
lactic acidduring the procedure
DO2Iduring the procedure
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