Background:  Pulse pressure variation (ΔPP) and systolic pressure variation (SPV) induced by mechanical ventilation have been proposed to detect hypovolaemia and guide fluid therapy. During laparoscopic surgery, chest compliance is decreased by pneumoperitoneum. This may affect the value of SPV and ΔPP as indicators of intravascular volume status. Thereby, we investigated the effects of pneumoperitoneum and hypovolaemia on SPV and ΔPP.Methods:  We measured ΔPP, SPV and the inspiratory (Δup) and expiratory (Δdown) components of SPV, at baseline, during pneumoperitoneum, during pneumoperitoneum and hypovolaemia and after the return to baseline conditions, in 11 mechanically ventilated rabbits. Pneumoperitoneum was induced by inflating the abdomen with carbon dioxide, and hypovolaemia was induced by controlled haemorrhage.Results:  Pneumoperitoneum induced an increase in SPV from 8.5 ± 1.6 to 13.3 ± 2.6 mmHg (+56%, P < 0.05) as a result of an increase in Δup from 2.0 ± 1.0 to 6.7 ± 2.1 mmHg (+236%, P < 0.05), but no significant change in Δdown, nor in ΔPP. Haemorrhage induced a significant (P < 0.05) increase in SPV from 13.3 ± 2.6 to 19.9 ± 3.7 mmHg (+50%), in Δdown from 6.6 ± 3.3 to 14.0 ± 4.9 mmHg (+112%) and in ΔPP from 11.1 ± 4.8 to 24.9 ± 9.8% (+124%) but no change in Δup. All parameters returned to baseline values after blood re‐infusion and abdominal deflation.Conclusions:  SPV is modified by haemorrhage but it is also influenced by pneumoperitoneum. In contrast, ΔPP is modified by haemorrhage but not by pneumoperitoneum. These findings suggest that ΔPP should be used preferentially instead of SPV to detect hypovolaemia and guide fluid therapy during laparoscopic surgery.

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Although this monitor had not been calibrated, it showed a tendency for consistent hemodynamic data in obstetric patients and it may be used as a therapeutic guide or experimental tool.

(Anesth Analg. 2018;127:165–170) Systemic clonidine [oral or intravenous (IV)] has been administered preoperatively for attenuation of perioperative hemodynamic instability and for reducing anesthetic and postoperative analgesic needs. However, IV clonidine has not been evaluated as an adjuvant during cesarean delivery. In the present study, the authors evaluated and compared the effectiveness of standard spinal anesthesia, standard spinal anesthesia combined with intrathecal clonidine, and standard spinal anesthesia combined with IV clonidine.

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