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Summary Table

Category	Detail
Risk Factors	Atherosclerotic disease of the vertebrobasilar system, hypertension, diabetes, hypercoagulable states, history of posterior circulation TIA. Less commonly: rapid correction of hyponatremia (central pontine myelinolysis), pontine hemorrhage, basilar artery dissection, pontine tumor, traumatic brain injury
Etiology	Bilateral destruction of the ventral pons, most commonly from basilar artery occlusion or thrombosis. The lesion destroys the corticospinal and corticobulbar tracts while sparing the tegmentum (reticular activating system) and the dorsal midbrain pathways for vertical gaze
Patient Presentation	A patient who appears unresponsive and "comatose" but is actually fully awake and aware. Family or nursing staff may notice the patient can blink on command or follow with vertical eye movements. The vignette may describe a patient who "stares at the ceiling" and was initially diagnosed as comatose
Classic Physical Exam	Quadriplegia (all four limbs flaccid or spastic), anarthria (inability to speak), preserved consciousness, intact vertical eye movements, preserved blinking. Horizontal eye movements are absent. The patient cannot move the face, chew, swallow, or produce speech
Key Diagnostic Results	MRI brain showing bilateral ventral pontine infarction or lesion with sparing of the tegmentum. EEG showing a reactive, normal or near-normal alpha rhythm (proving cortical awareness). CT or MR angiography demonstrating basilar artery occlusion
Management	Acute: if ischemic and within the treatment window, IV thrombolysis or endovascular thrombectomy of the basilar artery. Supportive: mechanical ventilation, enteral feeding, DVT prophylaxis, pressure injury prevention. Long-term: augmentative communication devices (eye-tracking systems), multidisciplinary rehabilitation
Keywords	"Awake but paralyzed," "can only blink," "vertical eye movements preserved," "ventral pons," "basilar artery occlusion," "normal EEG in an unresponsive patient," "quadriplegia with preserved consciousness"

1. Pathophysiology

Locked-in syndrome results from a lesion that selectively destroys the ventral (anterior) pons while leaving the dorsal pons (tegmentum) intact. Understanding this anatomy is the key to understanding every feature of the syndrome.

The ventral pons contains two critical fiber systems that run through it: the corticospinal tracts (which carry motor commands to the limbs and trunk) and the corticobulbar tracts (which carry motor commands to the cranial nerve nuclei controlling the face, tongue, pharynx, and larynx). When these tracts are destroyed bilaterally, the patient loses all voluntary movement of the body and all ability to speak, chew, or swallow. This produces quadriplegia and anarthria, which together make the patient appear completely unresponsive.

However, consciousness is governed by the ascending reticular activating system (ARAS), which is located in the tegmentum (the dorsal portion of the brainstem). Because the tegmentum is spared, the patient remains fully awake, alert, and cognitively intact. They can hear, see, understand language, feel pain, and think normally. They simply cannot express any of this through movement or speech.

The reason vertical eye movements and blinking are preserved is anatomical: the nuclei and supranuclear pathways controlling vertical gaze are located in the midbrain (the rostral interstitial nucleus of the medial longitudinal fasciculus and the posterior commissure), which sits above the level of the pontine lesion. In contrast, horizontal gaze is lost because the paramedian pontine reticular formation (PPRF) and the abducens nucleus (CN VI), both of which are essential for horizontal eye movements, are located within the pons itself and are damaged or disconnected by the lesion.

The most common cause is basilar artery thrombosis or occlusion, because the basilar artery supplies the ventral pons through its paramedian perforating branches. When these branches are occluded, the ventral pons infarcts while the tegmentum, which receives collateral blood supply from other sources, may be relatively preserved. Other causes include pontine hemorrhage, central pontine myelinolysis (from overly rapid correction of hyponatremia), brainstem tumors, and trauma.

The critical concept for exam purposes is this: the locked-in patient has intact cognition trapped inside a paralyzed body. They are not in a coma. They are not in a vegetative state. They are awake and aware but physically unable to demonstrate it except through vertical eye movements and blinking.

2. Classification and Clinical Manifestation

Classification	Motor Function	Eye Movements	Consciousness	Communication
Classic Locked-In Syndrome	Complete quadriplegia, complete anarthria, no facial movement	Vertical eye movements and blinking preserved; horizontal gaze absent	Fully preserved	Only through blinking and vertical eye movements
Incomplete Locked-In Syndrome	Near-complete paralysis but with remnants of voluntary movement (e.g., a finger, a toe, slight head movement)	Vertical eye movements preserved; may have partial horizontal gaze	Fully preserved	Through residual movements plus eye movements
Total Locked-In Syndrome	Complete quadriplegia and anarthria	No voluntary eye movements at all, no blinking	Fully preserved but extremely difficult to confirm	None apparent; diagnosis depends entirely on EEG and functional neuroimaging

Total locked-in syndrome is the most dangerous variant from a diagnostic standpoint because it can be indistinguishable from coma or brain death on bedside examination alone. The only way to identify preserved consciousness in this form is through EEG (which shows cortical activity consistent with wakefulness) or functional MRI / PET scanning (which may show cortical responses to stimuli). This is a tested concept: the question may describe a patient with no observable responses at all and ask what test would differentiate this from a vegetative state.

3. Diagnostic Workup

Test	Role	Key Finding
MRI Brain (with diffusion-weighted imaging)	Best Initial Imaging / Confirmatory for lesion localization	Bilateral ventral pontine infarction or lesion with tegmental sparing
CT Head (non-contrast)	Often the first study obtained in the emergency setting	May show hyperdensity of the basilar artery (dense basilar sign); poor sensitivity for early posterior fossa infarction
CT Angiography / MR Angiography	Evaluate vascular etiology	Basilar artery occlusion or thrombosis
EEG	Confirm preserved consciousness	Normal or near-normal reactive alpha rhythm, sleep-wake cycling
Conventional Angiography	Gold standard for vascular anatomy if intervention is planned	Basilar artery occlusion with possible collateral flow patterns
Serum Sodium	If central pontine myelinolysis is suspected	History of rapid sodium correction from a hyponatremic state

When a patient presents appearing unresponsive, the initial evaluation follows the standard protocol for altered mental status. A non-contrast CT of the head is typically the first study and is obtained to rule out hemorrhage. However, CT has notoriously poor sensitivity for acute posterior fossa ischemic lesions because of bone artifact from the petrous bones. The CT may appear normal in the early hours, or it may show the "dense basilar artery" sign, a hyperdense basilar artery on non-contrast CT suggesting acute thrombosis.

The best imaging test for confirming the diagnosis and localizing the lesion is MRI of the brain with diffusion-weighted imaging (DWI). This will show restricted diffusion in the bilateral ventral pons, confirming acute infarction. The tegmentum will appear spared on imaging, which correlates directly with the preserved consciousness.

CT angiography or MR angiography should be performed to evaluate the basilar artery. In the setting of acute basilar artery occlusion, this is not merely diagnostic but directly determines whether the patient is a candidate for endovascular intervention.

The test that clinches the diagnosis of locked-in syndrome (as opposed to coma or vegetative state) is the EEG. In coma, the EEG shows diffuse slowing or suppression. In a vegetative state, the EEG is abnormal. In locked-in syndrome, the EEG shows a preserved, reactive alpha rhythm and normal sleep-wake cycling, proving that the cortex is functioning normally. This is a classic exam question: the EEG result that does not match the apparent clinical picture is the clue.

If central pontine myelinolysis is on the differential, checking serum sodium and reviewing the clinical history for recent correction of hyponatremia is essential. MRI in central pontine myelinolysis shows a characteristic trident-shaped or bat-wing hyperintensity on T2/FLAIR in the central pons.

4. Management and Treatment

Phase	Intervention	Details
Hyperacute (ischemic cause)	IV Alteplase (if within 4.5 hours) or endovascular thrombectomy	Basilar artery occlusion may have an extended window for thrombectomy compared to anterior circulation strokes; decisions are often individualized
Acute Stabilization	Airway protection and mechanical ventilation	The patient cannot protect the airway due to bulbar paralysis; early intubation is critical
Acute Supportive	DVT prophylaxis, pressure injury prevention, enteral nutrition, bladder catheterization	Standard ICU-level care for an immobilized patient
Subacute/Chronic	Augmentative and alternative communication (AAC) devices	Eye-tracking communication boards, brain-computer interfaces; these are the primary means of restoring functional communication
Rehabilitation	Physical therapy, occupational therapy, speech therapy	Prevent contractures, maintain range of motion, optimize residual function if incomplete form
Psychosocial	Psychiatric support, patient and family counseling	The patient is fully aware and at high risk for depression and existential distress

Acute management depends entirely on the underlying cause. If the etiology is basilar artery occlusion, the patient is treated as an acute posterior circulation stroke. IV alteplase (0.9 mg/kg, maximum 90 mg, with 10% given as a bolus and the remainder infused over 60 minutes) is indicated if the patient presents within 4.5 hours of symptom onset. However, endovascular mechanical thrombectomy is the more relevant intervention for basilar artery occlusion, and current evidence supports thrombectomy even beyond the standard anterior circulation time windows in selected patients, often up to 24 hours or more if there is evidence of salvageable tissue on advanced imaging.

This is a testable point: basilar artery occlusion has a uniquely high mortality if untreated, and the treatment window for endovascular therapy may be more liberal than for anterior circulation large vessel occlusion. The "next best step" in an acute presentation with dense basilar sign on CT is urgent CT angiography followed by thrombectomy if occlusion is confirmed.

If the cause is central pontine myelinolysis, there is no reversal therapy. Management is supportive. Prevention is the key concept: sodium should not be corrected faster than 8 to 10 mEq/L per 24 hours in patients with chronic hyponatremia. If overcorrection occurs, re-lowering the sodium with desmopressin and D5W is the recommended approach.

Long-term management centers on supportive care and communication. The patient requires indefinite mechanical ventilation in many cases, though some patients with incomplete forms may eventually breathe independently. Communication aids are the most important long-term intervention: eye-tracking computer systems allow patients to communicate by selecting letters or words on a screen using vertical eye movements. The exam may test your knowledge that these patients are cognitively intact and that the appropriate next step in a stable locked-in patient is to establish a communication system, not to withdraw care based on an assumption of poor neurological function.

Contraindications and cautions: Thrombolysis is contraindicated in patients with active hemorrhage, recent surgery, or known coagulopathy. If the locked-in state is caused by pontine hemorrhage rather than ischemia, thrombolysis and thrombectomy are obviously contraindicated and the management is purely supportive with blood pressure control and surgical evaluation if there is obstructive hydrocephalus.

5. Differential Diagnosis and Distractors

Differential	Why It Is Similar	Key Discriminator
Persistent Vegetative State (Unresponsive Wakefulness Syndrome)	The patient appears unresponsive; may have eyes open and sleep-wake cycles, mimicking "wakefulness without awareness"	In vegetative state, the patient has no purposeful responses and the EEG is abnormal. In locked-in syndrome, vertical eye movements and blinking are purposeful and reproducible on command, and the EEG shows a normal reactive alpha rhythm
Coma	The patient appears completely unresponsive with no movement	In coma, the patient has no wakefulness at all (eyes remain closed), no sleep-wake cycling, and the EEG shows diffuse slowing or suppression. Locked-in patients have open eyes and normal EEG
Brain Death	No motor responses, no brainstem reflexes in some cases of total locked-in syndrome	Brain death requires absence of all brainstem reflexes (pupillary, corneal, oculocephalic, gag, cough) and a confirmatory test showing no cerebral blood flow or electrical activity. Locked-in patients retain pupillary responses and have a normal EEG
Akinetic Mutism	The patient is awake but makes no spontaneous movements and does not speak	Akinetic mutism results from bilateral medial frontal lobe or cingulate lesions. The patient may have intact motor pathways (can be provoked to move with strong stimulation) but lacks the drive or motivation to initiate movement. Locked-in patients are motivated to move but physically cannot
Acute Severe Guillain-Barre Syndrome	Can produce rapidly progressive quadriplegia and respiratory failure, making the patient appear locked in	GBS is a peripheral demyelinating process with areflexia, albuminocytologic dissociation on CSF, and abnormal nerve conduction studies. MRI brain is normal. Locked-in syndrome is a central lesion with a visible pontine abnormality on MRI
Severe Myasthenia Gravis Crisis	Can produce generalized weakness including bulbar weakness with preserved consciousness	Myasthenia has fluctuating weakness, positive acetylcholine receptor antibodies, decremental response on repetitive nerve stimulation, and responds to edrophonium. No pontine lesion on imaging

6. Traps and High-Yield Pearls

The single most common way students get questions about locked-in syndrome wrong is by confusing it with a vegetative state or coma. The vignette is deliberately designed to make the patient appear unresponsive, and the test-writer is evaluating whether you understand that an apparently "comatose" patient may be fully conscious. The critical clue is always the same: the patient demonstrates purposeful vertical eye movements or blinking on command. If the vignette mentions that a nurse noticed the patient "seemed to follow instructions by blinking" or "moved his eyes upward when asked," that is the locked-in syndrome vignette, and the expected answer involves recognizing preserved consciousness.

A second common trap involves the EEG finding. If the question presents an unresponsive patient and then provides an EEG showing a normal reactive alpha rhythm, the expected conclusion is locked-in syndrome, not "artifact" or "error." The normal EEG in the setting of apparent unresponsiveness is a contradiction that should trigger recognition of this diagnosis.

A third tested concept is the localization. The question may ask where the lesion is. The answer is always the ventral pons (bilateral basis pontis). If the stem describes a patient with preserved consciousness, quadriplegia, anarthria, and intact vertical gaze but absent horizontal gaze, the only anatomical localization that fits is the ventral pons. Any answer involving the cortex, thalamus, or midbrain is incorrect.

Finally, be cautious about the ethical and management implication. Because locked-in patients are fully aware, they have decision-making capacity. Questions may test whether you would appropriately involve the patient in decisions about their care (using their communication method) rather than deferring solely to surrogates. The core competency being tested is the recognition that locked-in syndrome is a motor output failure, not a consciousness failure, and that treatment decisions must respect the patient's autonomy.

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