British Journal of Anaesthesia, 1992, Vol. 69, No. 5 461-464
© 1992 The Board of Management and Trustees of the British Journal of Anaesthesia
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COMPARISON OF HYPERTONIC SALINE (5%), ISOTONIC SALINE AND RINGER'S LACTATE SOLUTIONS FOR FLUID PRELOADING BEFORE LUMBAR EXTRADURAL ANAESTHESIA
Départment d'AnesthésieRéanimationUniversité Paris Sud, H
pital Antoine Béclère Clamart, France
We have compared the haemodynamic effects of fluid preloading performed before lumbar extradural anaesthesia with isotonic saline (NS), 5% hy-pertonic saline (HS) and Ringer's lactate (RL) solutions in 30 ASA I patients undergoing minor orthopaedic surgery, allocated randomly to the three groups. All patients received an equal amount of sodium (2 mmol kg1. After fluid preloading, lumber extradural anaesthesia was performed (2 % lignocaine 6 mg kg1) and ephedrine was administered in order to maintain mean arterial pressure (MAP) > 80% of its control value. Both volume and duration of fluid preload were significantly less in group HS (760 (SD 25) ml, 8.8 (SD 2.9) min) than in the two other groups (NS: 903 (144) ml, 17.7 (3.3) min; RL: 932 (166) ml, 212 (6.0) min) (P < 0.05). The number of blocked segments and the total amount of ephedrine administered were similar in the three groups. Heart rate increased significantly in all groups immediately after the fluid preload and remained increased until the end the study (90 min). MAP was not affected by any fluid preload and its maximal decrease after lumbar extradural anaesthesia was similar in all groups. Infusion of 5% HS 2.3 ml kg1 was tolerated well and produced a significant (? < 0.05) but moderate hypernatraemia lasting 90 min after the end of fluid preloading. We conclude that HS may be useful when rapid fluid preloading is desired, in situations where excess free water administration is not desired. (Br. J. Anaesth. 1992; 69: 461464)
*Present address, for correspondence: Département d'AnesthésieRéanimation, Hopital SaintCamille, 2 Rue des Péres Camilliens, 94366 Bry sur Marne Cedex, France.
Presented in pan at the meeting of the American Society of Anesthesiologists, San Francisco, October 1991.
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