05Possible addresses
20+Single-breath screen
01First move: localize
00Shotgun panels ordered
BloodSweatxED
The Curbside · Neurology · Stop the blow-up

Weakness Has an Address.

The complaint is not the localization. Prove objective power loss. Check the bellows. Then place the lesion before you order the MRI.

First 10 Seconds.

Weak is a symptom. Power loss is a finding.
Ask better

What can you no longer do?

“What could you do yesterday that you cannot do today?” Walking, stairs, rising from a chair, lifting an arm, opening a jar, swallowing, or holding the head up gives the complaint anatomy.

Fatigue, malaise, and heavy legs are not automatically motor weakness. They still deserve an explanation, but not a reflex neuromuscular workup.

Examine fast

Make the deficit declare itself.

  • Pronator drift and finger taps.
  • Neck flexion, shoulder abduction, finger abduction.
  • Hip flexion, knee extension, ankle dorsiflexion.
  • Sit to stand and gait, when safe.

Abrupt focal weakness is a stroke pathway.

Do not let a localization framework slow reperfusion care. Establish last known well, check glucose, activate the stroke pathway, then refine the address in parallel.

The Three-Question Screen.

Three questions beat fourteen untargeted labs.
1

Is sensation involved?

A sensory level, saddle symptoms, or sphincter dysfunction points to cord. Distal sensory loss with reduced reflexes points toward peripheral nerve. No sensory loss favors NMJ, muscle, or anterior horn cell. It does not prove one.

2

Does it fluctuate?

Fatigable ocular, bulbar, neck, or proximal weakness with intact sensation is a neuromuscular junction pattern. Check ptosis, sustained upgaze, speech, cough, neck flexion, and single-breath count now.

3

What do the reflexes say?

Hyperreflexia, clonus, or Babinski suggests an established UMN lesion. Hyporeflexia suggests nerve or anterior horn cell. Normal reflexes with symmetric proximal weakness favors muscle or NMJ.

Weakness Address Map

Pattern + sensation + reflexes
Brain / cord
Asymmetric or level-based. Cortical signs, cranial findings, sensory level, sphincter symptoms, UMN signs.
Stroke, cord compression, myelopathy. Acute cord lesions can be flaccid before UMN signs appear.
Anterior horn
Pure motor. Atrophy and fasciculations. Sensation spared.
Mixed UMN and LMN findings across regions suggests motor neuron disease. Usually not an hours-to-days diagnosis.
Peripheral nerve
Distal or ascending. Sensory symptoms common. Reflexes reduced.
GBS, toxic or metabolic neuropathy, radiculopathy, mononeuropathy.
NM junction
Fatigable. Ocular, bulbar, neck, then generalized. Sensation spared.
Myasthenia, botulism, Lambert-Eaton, tick paralysis, organophosphate toxicity.
Muscle
Symmetric proximal. Sensation spared. Reflexes preserved until severe.
Inflammatory, toxic, endocrine, electrolyte, or rhabdomyolysis. CK helps, but the pattern comes first.

Do Not Miss Bellows Failure.

Normal oxygen does not clear the diaphragm.
Look now

The bedside respiratory exam.

  • Rapid shallow breathing or orthopnea.
  • Weak cough, dysphagia, nasal or staccato speech.
  • Accessory use or paradoxical abdominal movement.
  • Weak neck flexion or inability to lift the head.
Trend it

Trajectory beats one number.

Get serial FVC, NIF or MIP, and MEP when neuromuscular respiratory failure is possible. Facial or bulbar weakness can make the mouth seal unreliable.

Pulse oximetry and blood gas can stay normal until late. Rising CO₂ means the warning phase is ending.

<20Single-breath count is concerning
<20mL/kg vital capacity
>-30cm H₂O MIP or NIF
<40cm H₂O expiratory pressure

The 20 / 30 / 40 rule is a trigger, not a clearance test.

Call respiratory therapy and escalate early for bulbar dysfunction, weak cough, rapid progression, or declining serial values. Intubate the patient, not the spreadsheet.

RSI Drug Traps.

The paralytic is part of the diagnosis.
Denervation

No succinylcholine.

Progressive neuromuscular disease, chronic weakness, GBS, and prolonged immobilization can produce dangerous hyperkalemia after succinylcholine.

ENLS alternative: rocuronium 1.0 to 1.4 mg/kg IV. A practical RSI dose is 1.2 mg/kg IV.

Myasthenia

Both classes can surprise you.

Succinylcholine may be relatively ineffective. Nondepolarizers can cause exaggerated and prolonged blockade.

ENLS suggests rocuronium 0.5 to 0.6 mg/kg IV. Expect prolonged weakness. Use quantitative monitoring and have a reversal plan when available.

GBS can swing hard.

Autonomic instability can produce bradycardia, tachyarrhythmia, or abrupt blood-pressure shifts. Put atropine or glycopyrrolate and a vasopressor within reach. Give fluid deliberately.

Patterns That Change the Call.

Name the pattern before the panel.
Peripheral nerve

Progressive symmetric weakness + hyporeflexia.

Think GBS, with or without paresthesias. It is a clinical diagnosis. LP and electrodiagnostics support it. Normal CSF protein early does not exclude it.

NM junction

Fatigable ocular or bulbar weakness.

Think myasthenia when sensation is intact and pupils are normal. Respiratory metrics and bulbar function drive the level of care.

Public health emergency

Descending paralysis + cranial palsies + autonomic signs.

Think botulism. Pupillary dysfunction and dry mouth help separate it from MG. Call the health department now. Do not wait for laboratory confirmation or antitoxin testing.

Muscle

Symmetric proximal weakness with intact sensation.

Think myopathy. CK, medication and toxin review, thyroid testing, and electrolytes can be targeted to the story. A normal CK does not erase every myopathy.

Do not overcall it

Fasciculations are a clue, not an ED diagnosis of ALS.

ALS requires progressive motor impairment with UMN and LMN dysfunction after alternatives are excluded. Mixed findings without sensory loss deserve neurology follow-up or admission when function, swallowing, or breathing is threatened. Catch the pattern. Do not label the patient from one twitch.

Disposition Without Regret.

Can they walk, swallow, and ventilate?
Admit or higher

Any unstable trajectory.

  • Rapid progression or serial exam decline.
  • Bulbar or respiratory involvement.
  • Autonomic instability.
  • Cannot walk safely or perform basic function.
  • Possible GBS, myasthenic crisis, botulism, or acute cord disease.
Discharge can fit

No objective deficit. Safe function.

Discharge only when strength and gait are normal, no bulbar or respiratory red flags exist, a dangerous central or neuromuscular process is not suspected, and the non-neurologic complaint has a safe plan.

Give explicit return precautions for new focal loss, progression, falls, dysphagia, dyspnea, weak cough, or inability to rise or walk.

Epic Note Starter.

Document the localization, not the complaint.
Acute weakness exam
Patient describes loss of function as: [FUNCTION]. Onset/trajectory: [LKW / PROGRESSION].

Objective strength: [PROXIMAL / DISTAL / SYMMETRY / MRC]. Gait: [SAFE / UNSAFE / UNABLE].
Mental status/cranial nerves: [FINDINGS]. Tone/reflexes/plantars: [FINDINGS].
Sensation: [NORMAL / DISTRIBUTION / LEVEL]. Bulbar exam/cough: [FINDINGS].
Neck flexion: [FINDING]. Single-breath count: [NUMBER].
FVC: [mL/kg]. NIF/MIP: [cm H₂O]. Serial trend: [TREND].

Working localization: [CENTRAL / ANTERIOR HORN / NERVE / NMJ / MUSCLE / NON-MOTOR].
Time-sensitive concern and action: [STROKE / CORD / GBS / MG / BOTULISM / OTHER].

Sources.

Updated July 2026