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August
1997
Nicardipine
versus nitroprusside for controlled hypotension during spinal surgery
in adolescents.
Hersey
SL, O'Dell NE, Lowe S, Rasmussen G, Tobias JD, Desphande JK, Mencio G,
Green N; Anesth Analg 1997;84:1239-44.
[ see
abstract below
]
This is an interesting
paper because it examines this group's experience with two techniques
for induced hypotensive anesthesia. The authors prospectively compared
sodium nitroprusside versus the calcium channel blocker nicardipine. Both
groups were evenly matched for age, weight, and operative time.
Two differences were found:
- blood loss was
significantly greater in the nitroprusside group (1,298 � 264 vs 761
� 199 ml - p < 0.05);
- the time to restoration
of mean arterial blood pressure was longer in the nicardipine group
(26.8 � 4.0 vs 7.3 � 1.1 min - p < 0.002).
The authors concluded
that controlled hypotension could be easily achieved with nicardipine
but that there is a slow return to baseline blood pressure and a reduction
in blood loss. On the surface this sounds good, but the paper still leaves
the reader with a few questions.
Since patients were not monitored with central venous catheters, and since
the study was an open label design (the anesthesiologists knew the technique),
how can we be certain that observer bias did not influence the transfusions
administered? Had central venous pressure been monitored and patients
transfused to the same objective endpoint, then perhaps we would have
more confidence in this observation.
Another concern which was not commented upon was what effect if any does
nicardipine induced hypotension have on spinal cord blood flow and the
distribution of cerebrocortical blood flow? It is known that there are
significant differences between cortical blood flow distribution when
nitroprusside is compared to ganglionic blockade induced with trimethaphan.
Although these differences are of theoretic concern, one should not be
too quick to jump into a new technique until important information is
available; Hersey, et al are to be congratulated for starting the ball
rolling. I would hope that they or other investigators examine both spinal
cord and cerebral blood flow changes before generally advocating this
technique.
The time it took for restoration of normal arterial blood pressure brings
up an additional concern. Whenever major and massive blood loss is a possibility,
easy reversibility of the hypotensive agent is an advantage; nicardipine
would not appear to have this advantage and may in fact present a disadvantage.
When this situation occurs, even nitroprusside can seem to take an inordinate
period of time to wear off. I would hate to have to wait 25 minutes to
return to normal in this circumstance.
Perhaps an acceptable middle ground would be to use lower doses of nicardipine
and lower doses of nitroprusside combined. This would reduce the exposure
to nitroprusside while at the same time minimizing the potential for adverse
effects due to higher doses of single agents. I do not mean to be a therapeutic
nihilist, but I am always concerned about reaching wide based conclusions
based on a small number of patients.
Return to the Current
Literature Review Front Page, or read the abstract:
ABSTRACT
Nicardipine or nitroprusside was used to induce controlled hypotension in
healthy adolescents with idiopathic scoliosis undergoing spinal fusion.
Twenty patients were randomly assigned to the nitroprusside (N) or nicardipine
(C) group. All patients received a standardized anesthetic. A target mean
arterial blood pressure (MAP) of 60mm Hg was achieved by varying the vasoactive
infusions only. Moderate hemodilution (PCV = 25) and intraoperative blood
salvage were used in all cases. Hemodynamic variables, blood loss, occurrence
of reflex tachycardia, and reversibility of the hypotensive state were compared
between the two groups.
Significant differences were observed between the two groups in the amount
of blood loss and reversibility of the hypotensive state. Group C had less
blood loss (761 +/- 199 mL) than Group N (1297.5 +/- 264, P </= .05).
Time to restoration of baseline MAP was longer with Group C (26.8 +/- 4.0
min) than Group N (7.3 +/- 1.1 min, P </= 0.001).
Both drugs rapidly achieved a stable controlled hypotensive state and an
acceptable operating field. There was no statistically significant difference
between groups with respect to the amount of crystalloid administered or
urine output.
These results suggest that nicardipine is a safe, effective drug for controlled
hypotension in this population and that it may offer the significant advantage
of reduced blood loss in these patients.
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