3.29 Stress Response to Surgery Flashcards
Stress response
is the term used to describe the widespread metabolic and hormonal changes
which occur in response to trauma,
including surgical trauma.
It is a complex neuroendocrine response whose net effect
is to increase catabolism and release endogenous fuel stores
while conserving body fluids.
In evolutionary terms, it is a natural mechanism which
increases an injured animal’s chances of survival.
The degree of catabolism
The degree of catabolism is related to the severity of the surgical insult
or traumatic tissue injury.
In practice, the plasma concentrations of most substances increase,
and it is unlikely that the examiner will ask you specifically about a single
hormone.
If this does happen, and you do not immediately know the answer, or
you suspect that it is a trick question, then try to answer it from first principles.
Do not be concerned if your reply does not seem that logical; it is not clear, for
example, why prolactin concentrations should increase while thyroid hormone
should rise little, if at all
Endocrine response
1 Autonomic nervous system – sympathoadrenal response
2 Hypothalamic–pituitary–adrenal (HPA) axis
- Cortisol
- Insulin
- Inflammatory response
Autonomic nervous system – sympathoadrenal response
This is mediated via the hypothalamus
with the stimulation of adrenal medullary catecholamines.
There is also increased presynaptic noradrenaline release.
This leads to cardiovascular stimulation with tachycardia
and peripheral vasoconstriction.
The renin–angiotensin system stimulates aldosterone release,
leading to sodium and water retention.
Hypothalamic–pituitary–adrenal (HPA) axis
Hypothalamic releasing factors respond to major surgical trauma
by stimulating the anterior pituitary.
This in turn leads to increases in adrenocorticotrophic hormone (ACTH)
which stimulates adrenal glucocorticoid release,
and somatotrophin (growth hormone).
This enhances protein synthesis and inhibits breakdown,
stimulates lipolysis and antagonizes insulin.
Prolactin release is also evident,
although its purpose is not obvious.
The other anterior pituitary hormones, including thyroid hormone, change little.
The posterior pituitary produces increased amounts of
arginine vasopressin (antidiuretic hormone, ADH).
Cortisol:
Release from the adrenal cortex after stimulation by ACTH
may increase fourfold,
and this leads to intense catabolism in which there is protein breakdown,
increased gluconeogenesis and lipolysis, with inhibition of glucose utilization.
Cortisol is anti-inflammatory:
it inhibits leucocyte migration into damaged areas
and inhibits synthesis of various inflammatory mediators,
including prostaglandins.
Insulin
This is the major anabolic hormone of which there is a relative
perioperative deficiency. Its effects are unable to match the catabolic response.
Inflammatory response
After major tissue trauma, a number of cytokines are released
(including IL-1, IL-6, TNF and interferons).
IL-6 is the cytokine mainly responsible for the development of the
systemic ‘acute phase response’.
Modification of the response by anaesthesia
Catabolism provides endogenous fuel from
carbohydrate, fatty acids and amino acids, with the loss of body nitrogen.
The process is accompanied by sodium and water retention.
As an evolutionary process this may have conferred a survival
benefit, but this must apply less in the context of modern surgery and anaesthesia.
In the elderly surgical population with patients with significant co-morbidity, the
stress response may have obvious adverse effects.
Whether or not anaesthetists should be trying to ablate the response, however, remains contentious.
Opiates:
these suppress hypothalamic and pituitary secretion,
and high-dose
opiates (for example,
morphine in a dose of 4mg/kg or
fentanyl in a dose of 100 ug/kg
may attenuate the response substantially,
but this is at the cost of profound sedation and respiratory depression.
The effect does not endure.
Etomidate
Etomidate: this drug is an effective inhibitor of cortisol and aldosterone synthesis
via its inhibition of the 11-b and 17-a hydroxylase steps of steroid synthesis. This
inhibition persists for 6–12 hours after a single dose.
BZD
A2 agonists
Benzodiazepines: these also inhibit cortisol production, probably via a central effect.
a-2 agonists:
these attenuate the sympathoadrenal responses,
and lead indirectly to a decrease in cortisol production.
Regional anaesthesia
This is of continued interest because it has been demonstrated
that extensive extradural block ablates the adrenocortical and
glycaemic responses to surgery.
It may be more difficult to achieve in upper gastrointestinal tract and thoracic surgery,
but there is increasing acceptance of the claim
that targeted and sustained regional anaesthesia has beneficial effect on
surgical outcome.
This, however, may be related as much to earlier ambulation
and improvements in respiratory function as to the abolition of the stress
response itself.