Lecture 4: Headaches in the ED Flashcards

1
Q

Red Flags in History for ED pt presenting with HA

A
  • Age < 5 or > 50 with new/worsening HA
  • Sudden onset thunderclap (Cerebral aneurysm)
  • Sudden onset with exertion (SAH, Arterial dissection)
  • Fever with HA onset (meningitis)
  • Different quality HA
  • Usage of bloodthinners (risk of hemorrhage)
  • Recent ABX use (may lessen clinical presentation)

Sudden varies, dependent on condition.

Sudden for thunderclap = seconds!

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2
Q

What is considered analgesic overuse when it comes to HAs?

A

> 10 times a month = risk of rebound HA

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3
Q

What illegal substances can increase risk of hemorrhage in HAs?

A
  • Cocaine
  • Amphetamine
  • Methamphetamine
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4
Q

What combination on PE might suggest meningitis?

A
  • HA (esp if it persists despite control of fever)
  • Fever
  • Neck stiffness
  • AMS
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5
Q

What fundoscopic finding suggests increased ICP?

A

Optic desk papilledema = increase ICP

Acute angle closure glaucoma

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6
Q

What might meningismus suggest?

A
  • Infection
  • Hemorrhage
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7
Q

What should ALWAYS BE PERFORMED for a patient with HA?

A

Neurologic exam

Must do CN exam, motor, sensation, gait, DTRs

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8
Q

What associated conditions are concerning with presence of HA?

A
  • Pregnancy
  • SLE
  • Behcets
  • Vasculitis
  • Sarcoidosis
  • Cancer

Immunosuppressed patients. Consider infection.

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9
Q

What labs are recommended for a high risk pt presenting with HA?

A
  • CBC w/ blood cultures (suspected infection)
  • CMP
  • Coag panel (suspected bleed or need for LP)
  • ESR/CRP (temporal arteritis)
  • hCG
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10
Q

When is non-con head CT indicated for HA eval?

A
  • Abnormal neurologic exam
  • New/severe HA of sudden onset
  • HIV+ with new HA
  • Concerned for increased ICP in pt requiring an LP
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11
Q

Indication for LP in evaluation of ED pt with HA

A
  • Meningitis
  • Encephalitis
  • Intracranial hypotension
  • Pseudotumor cerebri
  • SAH (if CT was neg but still sus)

CT scan is reliable within 6 hrs of hemorrhage for SAH

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12
Q

MCC of people presenting to ED with HA

A

Primary HAs: Migraine, cluster, tension

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13
Q

Migraine presentation

A
  • Slow onset, over 72h usually
  • MC aura types are lightheaded or visual changes
  • unilateral throbbing/pulsatile
  • Worsens with physical activity
  • N/V, photophobia, phonophobia

MC overall

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14
Q

Migraine Management in the ED

A
  • Analgesic + antiemetic + antihistamine = first line
  • Ketorolac + prochlorperazine + diphenhydramine
  • Dexamethasone used to reduce risk of recurrence

OK to use metoclopramide too instead.

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15
Q

When are triptans indicated in migraine management in ED?

A
  • No usage prior to arrival.
  • CI in pregnancy, CAD, uncontrolled HTN, or CVD

Causes vasoconstriction. Sumatriptan SC or IN.

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16
Q

When are ergot derivatives indicated in migraine management?

A
  • Requires pretx with antiemetic +/- antihistamine
  • CI in HTN, IHD, PAD, Pregnancy

DHE4 + metoclopramide +/- diphenhydramine

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17
Q

Management of a pregnant pt with migraine in the ED

A
  1. Acetaminophen, Opioids, metoclopramide, corticosteroids
  2. NSAIDs ok in 1st and 2nd trimesters.
  3. CI: Triptans, ergotamines, caffeine (Excedrin)
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18
Q

Prevention of migraines post ED tx

A
  • Sumatriptan
  • Midrin

Take triptan as soon as pain begins.

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19
Q

Presentation of cluster HA in the ED

A
  • unilateral, excruciating pain
  • Pain lasts 12min-180min w/o tx
  • Ipsilateral symptoms: lacrimation, conjunctival infection, nasal congestion, edema, sweating
  • Recurring daily for > week and remitting for 4+ weeks
  • Can be precipitated by ETOH or vasodilators
  • Normal neuro

Often located periorbital.

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20
Q

Management of cluster HA in ED

A
  1. High flow O2 12LPM via NRB
  2. Sumatriptan if O2 doesn’t resolve
  3. Last resort: IN lidocaine, oral ergotamine/caffeine, IV DHE 45
21
Q

Transitional therapy for cluster HA in ED

A
  • Tapered prednisone over 2wks
  • Naratriptan BID
  • Ergotamine QHS or BID

F/u with neurology afterwards.

22
Q

Presentation of tension HA in ED

A
  • Gradual onset
  • Diffuse, band-like, vise-like (occipital/frontal)
  • Duration: Hours to days
  • Mild nausea and photophobia
  • Prior: Tension, stress, fatigue
  • Normal neuro
23
Q

Management of tension HA in ED

A
  1. NSAIDs/non-opioid analgesic +/- caffeine +/- antiemetic/sedative
  2. Muscle relaxant if muscle tension noted (only take at night due to sedative effects)

PCP f/u

Ketorolac + compazine/reglan + diphenhydramine
Excedrin OTC for OP use
Take medication as soon as you start feeling pain!

24
Q

Presentation of brain tumor

A
  • Mild HA, deep aching in nature
  • Early on: no focal neuro deficits, HA increasing in frequency/duration CLASSIC
  • Later: constant pain, focal neuro deficits
  • Worsens upon awakening and with valsalva
25
What can confirm dx of brain tumor in the ED?
**CT scan with con** or MRI if available
26
Management of brain tumor in ED
* Neurosurg consult for large, symptomatic, signs of increased ICP, or impending herniation * IV glucorticoids (dexamethasone) to reduce cerebral edema * **secondary** Antiseizure agent (keppra, topa, lamo, VPA, lacosamide) * Secure airway if herniation is impending on imaging | Only use secondary if a seizure occurs.
27
Presentation of post-trauma HA/post concussive syndrome
* **Hx of Head injury** * Variable onset of pain * Non-specific HA (similar to tension or migraine) * Fatigue, dizziness, vertigo, insomnia, personality changes, etc
27
Evaluation of post-traumatic headache
**CT w/o con** if no previous evaluation yet
28
Management of post-traumatic HA
* Simple = d/c home and f/u with PCP. Usage of nonopiate analgesics or antiemetics * Avoid activity that could lead to second injury or worsen symptoms. * Need to gradually return to baseline physical activity
29
Main characteristics of Idiopathic intracranial HTN/pseudotumor cerebri
Syndrome characterized by * Papilledema * Increased ICP * Normal/small-sized ventricles on imaging
30
Presentation of Idiopathic Intracranial HTN
1. **HEADACHE** 2. Transient visual obscurations 3. Pulsatile tinnitus 4. Scotoma/scintillations 5. Back pain 6. Retrobulbar pain 7. Diplopia 8. Sustained visual loss, which can become permanent | In order of frequency! ## Footnote PE will show papilledema, visual field loss, and 6th CN palsy.
31
How does 6th CN palsy present?
Loss of lateral gaze
32
Dx of Idiopathic Intracranial HTN
* CT scan of brain w/o con = normal * **LP with opening presure > 25cm h2o for adults or 28 in children.** * LP with normal CSF | Must educate pt to avoid valsalva during LP opening ## Footnote **Opening pressure must be performed in lateral decubitus with knees extended!**
33
Managment of Idiopathic Intracranial HTN
1. **Preserve vision** 2. Remove CSF until opening pressure = 10-20 cm H2O. 1mL CSF = 1 cm H2O 3. Oral acetazolamide +/- thiazide 4. If a new Dx = admit 5. If old Dx = consult neuro | Acetazolamide = reduction of CSF production ## Footnote Avoid serial LPs
34
Presentation of PDPH/intracranial HYPOtension
* **Recent hx of LP** (MC etiology) * 24-48h of post-LP * Bifrontal/occipital * **Worse in upright position, improving in supine** * Auditory, visual, N/V, neck stiffness, LBP, vertigo, dizziness | Leakage of CSF and absorption into surrounding tissue.
35
Dx of post-dural puncture HA (PDPH)/intracranial hypotension
* Avoid repeating LP. * If LP is repeated, opening pressure will be very low at < 6cm H2O * No need for MRI/CT, but it will show **diffuse enhancement of the meninges** | WikEM says dx is clinical if it was post-LP. ## Footnote Spontaneous intracranial hypotension needs LP or MRI/CT
36
Management of PDPH
* **Recumbent position for a day** * IVF * Non-opiate analgesics +/- **caffeine** * Consult anesthesiology for need for epidural blood patch ## Footnote Injection of pt's blood over opening to clot.
37
MC ways for brain abscess to form
* Hematogenous spread * Direct contiguous infection * Direct seeding by neurosurgery * Penetrating trauma
38
Presentation of brain abscess
* HA * Focal neurologic deficits * Fever * Seizure * S/S of increased ICP | Similar to meningitis?
39
Workup for a Brain abscess
1. **CT or MRI brain w/ con is diagnostic** 2. CBC (leukocytosis) 3. CMP (end organ function) 4. CRP/ESR elevated in 2/3 of pts 5. Blood cultures 2x before first abx | **Avoid LP**
40
Management of brain abscess
1. Odontogenic = PCN G (rocephin + metro) 2. Post-neuro procedure: vanco + cefatzidime 3. Anything else: Cefotaxmine + metro 4. **Steroids only if significant peri-abscess edema w/ associated mass effect and increased ICP** 5. Need neurosurg to consider aspiration | Based on suspected source ## Footnote Steroids will dissolve abscess wall!!!!!!!!
41
MC location for spinal epidural abscess
* Thoracic * Lumbar
42
MCC of spinal epidural abscess
**Hematogenous spread from soft tissue (MC S. aureus)**, urine, or respiratory
43
Risk factors for spinal epidural abscess
* IVDU * Immunosuppressed * Prior spinal procedure
44
Presentation of spinal epidural abscess
* Early: Back pain, fever, spinal tenderness * Later: Radicular pain, hyperreflexia, nuchal rigidity * **Progressive neuro deficits (Cauda Equina)**
45
Cauda Equina Mnemonic
* Saddle anesthesia * Pain (lower back/lower limbs) * Incontinence (stool/urine) * Numbness (groin/legs) * Emergency (surgery) | SPINE ## Footnote Check rectal tone, motor weakness, and perineal sensation
46
Dx of spinal epidural abscess
* **MRI w/ con of spine** (CT if no MRI available) * CBC (Leukocytosis in most) * Elevated ESR/CRP * Blood cultures | LP is CI if epidural abscess is suspected
47
Management of spinal epidural abscess
* Empiric ABX: Vanco + ceftazidime (same as post-neuro brain abscess) * Consult neurosurg