Editor—In their study investigating intravascular volume optimisation and proximal femoral fracture, Sinclair et al have a different approach to fluid replacement between the two groups studied.1 The control group received only a median volume of 1000 ml of crystalloid (presumably Hartmann’s or 0.9% saline solution) peroperatively. As only about a quarter of this solution is retained intravascularly, these patients effectively had a depleted intravascular volume perioperatively. In contrast, the protocol group received a median of 750 ml of colloid as well as 725 ml of crystalloid, giving intravascular fluid replacement of nearly 1 litre. The preoperative dextrose-saline maintenance fluids would have had minimal effect on the intravascular volume: only 15% of such a solution is retained within the intravascular compartment.
This study merely shows that patients who have not received fluid or who have fluid depletion have a higher rate of complications, which is not a surprising or new finding. A control group should be recognisable as such; if the control group has been deprived of fluid then this will magnify any benefits in the protocol group. We suggest that if adequate preoperative intravascular fluids, and not just dextrose-saline maintenance fluids, had been given to all patients, replacing the blood loss associated with femoral fractures (often in excess of 1 litre2), then the differences between the groups would have been much less. A study comparing a group in whom optimisation is used with a group given sufficient fluid would be of much greater importance and would show the benefits of optimisation more clearly.
References
- 1.Sinclair S, James S, Singer M. Intraoperative intravascular volume optimisation and length of hospital stay after repair of proximal femoral fracture: randomised controlled trial. BMJ. 1997;315:909–912. doi: 10.1136/bmj.315.7113.909. . (11 October.) [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Willet KM, Dorrell H, Kelly P. ABC of major trauma: Management of limb injuries. BMJ. 1990;301:229–233. doi: 10.1136/bmj.301.6745.229. [DOI] [PMC free article] [PubMed] [Google Scholar]
