In hemorrhagic shock, which of the following physiologic responses occurs first as a result of sympathetic activation?
A. Oliguria and reduced urine output
B. Altered mental status and confusion
C. Systolic blood pressure falls below 90 mmHg
D. Vasoconstriction and increased heart rate
Explanation
Pathophysiology of Hemorrhagic Shock — Sequence of Compensation
Key Point
Hemorrhagic shock progresses through a predictable sequence of compensatory mechanisms. Sympathetic activation is the first and earliest response to blood volume loss, occurring before systemic hypotension develops.
Timeline of Compensatory Mechanisms
1.
Immediate (within seconds): Sympathetic nervous system activation
Early (minutes): Fluid shifts and hormonal response
Interstitial fluid shifts into intravascular space
Activation of renin–angiotensin–aldosterone system (RAAS)
ADH (vasopressin) release
Increased respiratory rate (tachypnea)
3.
Late (if uncompensated): Decompensation and organ hypoperfusion
Systolic BP falls (loss of compensation)
Altered mental status (cerebral hypoperfusion)
Oliguria (renal hypoperfusion)
Metabolic acidosis (tissue hypoxia)
Mechanism of Sympathetic Compensation
High-YieldNEET PG
The baroreceptor reflex is triggered by a decrease in mean arterial pressure detected by carotid sinus and aortic arch baroreceptors. This activates the sympathetic nervous system via the brainstem, resulting in:
Vasoconstriction: Preferential perfusion of vital organs (brain, heart, kidneys)
In Class I and II hemorrhagic shock, systolic blood pressure remains normal or only mildly reduced because sympathetic compensation is adequate. The presence of tachycardia and tachypnea in a normotensive patient is a sign of early shock and should prompt aggressive resuscitation before decompensation occurs.
Mnemonic: "SAVE the vital organs"
Sympathetic activation (first response)
Arteriolar vasoconstriction
Venous constriction
Elevated heart rate and contractility
These mechanisms preserve perfusion to the brain, heart, and kidneys at the expense of skin, GI tract, and skeletal muscle.
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