Editorials

Reducing the risk of major elective surgery

Optimising oxygen delivery before surgery does work; now we have to implement it

Papers p   1099

In this week's BMJ Wilson and colleagues report a randomised controlled trial in high risk surgical patients admitted to an intensive care unit at least four hours before elective operation for optimisation of cardiac output and oxygen delivery to >600 ml/min/m². This pre-emptive strategy was compared with usual practice, which is to monitor the cardiovascular system intraoperatively and to respond to changes in arterial and filling pressures. They showed a reduction in mortality from 17% (95% confidence interval 8% to 31%) to 3% (0.7% to 9%) and reduction of bed use by up to 40% (p 1099).¹ By the usual criteria their patients were high risk: about a third had known ischaemic heart disease and half of them were aged over 70. This finding is not unexpected, and the question now is what we should do about it.

Control of the circulation is one of the first tutorials in cardiovascular physiology. We teach how baroreceptors sense the resulting pressure between the force of the contracting heart and the resistance of the peripheral vasculature, illustrating the concept of negative feedback. While concentrating on arterial pressure, it is easy to forget that flow matters most, for it is that which determines oxygen delivery. Pressure tells us little about tissue perfusion: a surgeon will demonstrate for you the normal pressure in a completely occluded artery.

The opportunity to measure and intervene provided by the development of open heart surgery in the 1950s showed cardiac output to be the critical determinant of survival. ² From the late 1960s the Guy's team advocated a combination of pharmacological manipulation and volume repletion to optimise flow. In clinical practice we used right atrial pressure to guide filling and big toe temperature to judge tissue perfusion; the pharmacological innovation was vasodilatation with small bolus doses of chlorpromazine.³ Kirklin's group investigated means of maximising cardiac output by nitroprusside infusion and volume repletion, using left atrial pressure and dye dilution, refining the method but not changing the message.⁴

Anaesthetic and surgical teams quickly recognised that these lessons learnt in cardiac surgery were applicable to trauma management and emergency surgery. Central venous pressure measurement entered the repertoire, and resuscitation to volume repletion became the norm. Applying this to major elective surgery was logical. More of a challenge was the contention that elective patients should be admitted to an intensive care unit to have pulmonary artery and peripheral arterial catheters inserted, to be volume loaded, and to be treated with infusions of drugs to prepare them for major surgery.⁵ The study by Shoemaker et al reported dramatic reductions in mortality,⁵ a benefit replicated by Boyd et al⁶ and now confirmed again by Wilson et al.¹ The background mortality in similar patients outside the trials is about 40%.⁵

There is a difficulty in deciding the clinical protocol for the control groups in randomised trials, other than that it should accord with best conventional practice. Mortality in control patients ranged from 17% to 28% (37/160 patients in all). In the optimised groups mortality was 3%,¹ 4%,⁵ and 6%.⁶ In line with the reduction in mortality were reductions in morbidity and hospital stay, in the most recent study from an average of 22 days for the control group to 13 days for those optimised with dopexamine.

There has been resistance to implementing optimisation protocols in clinical practice. Concern exists about the use of inotropes outside of the rescue of patients from cardiac arrest or profound hypotension, with a shop floor view that, as with many things in life, you do not get something for nothing, and there will come a payback time. Inotropes increase myocardial oxygen consumption, and there are examples of subendocardial ischaemia. In the double strategy of volume repletion and drug infusion, the "inodilator" dopexamine had advantages over adrenaline as the pharmacological side of the package,¹ and cardiac experience emphasises the use of dilators to aid delivery^2-4 rather than inotropes to drive it. Dopexamine may also have a role in reducing detrimental inflammatory responses.¹

There has also been anxiety about the risks of pulmonary artery flotation catheters. ^{7 8} Trials of optimisation point consistently to benefit, ^{1 5 6 9} which has also been the case when flow is measured by less invasive doppler techniques in orthopaedic¹⁰ and cardiac patients.¹¹ The benefits of optimisation protocols have been replicated outside trials.¹²

In England, Wales, and Northern Ireland almost 20 000 patients a year die within 30 days of a surgical procedure.¹³ The findings of Wilson et al's study are important to all involved in providing resources as well as to those who care for these patients. Apart from reluctance to change practice, a major obstacle may be the limited resource of intensive care beds. When accident and emergency departments cannot find beds for emergencies, there is an understandable resistance to using intensive care units for all high risk elective cases. However, if it is agreed that the evidence is there to support the practice of optimisation its cost will have to be calculated into the price of operating on these patients. The benefits in survival, reduced morbidity, and shorter hospital stay are striking enough to justify it.

Tom Treasure, Professor of cardiothoracic surgery. 
David Bennett, Professor of intensive care. 

St George's Hospital Medical School, London SW17 0QT

1. Wilson J, Woods I, Fawcett J, Whall R, Dibb W, Morris C, et al. Reducing the risk of major elective surgery: randomised controlled trial of preoperative optimisation of oxygen delivery. BMJ 1999; 318: 1099-1103[Abstract/Free Full Text].
2. Boyd AD, Tremblay RE, Spencer FC, Bahnson HT. Estimation of cardiac output soon after intracardiac surgery with cardiopulmonary bypass. Ann Surg 1959; 150: 613-626[Medline].
3. Pagliero KM, Yates AK, Hill DG. The controlled use of vasodilator drugs in the management of hypovolaemia complicated by diminished cardiac function. Br J Surg 1973; 60: 201-203[Medline].
4. Appelbaum A, Blackstone EH, Kouchoukos NT, Kirklin JW. Afterload reduction and cardiac output in infants early after intracardiac surgery. Am J Cardiol 1977; 39: 445-451[Medline].
5. Shoemaker WC, Appel PL, Kram HB, Waxman K, Lee T-S. Prospective trial of supranormal values of survivors as therapeutic goals in high risk surgical patients. Chest 1988; 94: 1176-1186[Abstract/Free Full Text].
6. Boyd O, Grounds M, Bennett ED. A randomized clinical trial of the effect of deliberate perioperative increase of oxygen delivery on mortality in high-risk surgical patients. JAMA 1993; 270: 2699-2707[Abstract].
7. Connors Jr AF, Speroff T, Dawson NV, Thomas C, Harrell FEJ, Wagner D, et al. The effectiveness of right heart catheterization in initial care of critically ill patients. JAMA 1996; 276: 889-897[Abstract].
8. Soni N. Swan song for the Swan-Ganz catheter? BMJ 1996; 313: 763-764[Free Full Text].
9. Berlauk JF, Abrams JH, Gilmour IJ, O'Connor SR, Knighton DR, Cerra FB. Preoperative optimization of cardiovascular hemodynamics improves outcome after peripheral vascular surgery. A prospective, randomised clinical trial. Ann Surg 1991; 214: 289-297[Medline].
10. 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[Abstract/Free Full Text].
11. Mythen MG, Webb AR. Perioperative plasma volume expansion reduces the incidence of gut mucosal hypoperfusion during cardiac surgery. Arch Surg 1995; 130: 423-429[Abstract].
12. Curran JE, Grounds RM. Ward versus intensive care management of high-risk surgical patients. Br J Surg 1998; 85: 956-961[Medline].
13. Gray AJ, Hoile RW, Ingram GS, Sherry KM. The report of the National Confidential Enquiry into Perioperative Deaths 1996/1997. London: Royal College of Surgeons, 1997:118.