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Phys Written Answersneurological

Phys Written Answers · neurological

Headache — Written Clinical Reasoning

DCE long-case preparation: structured written reasoning for thunderclap headache and subarachnoid haemorrhage workup, giant cell arteritis urgent management, chronic migraine with medication overuse, and idiopathic intracranial hypertension diagnostic reasoning.

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Target exams

FRACP DCEMRCP Part 2

Target exams

FRACP DCEMRCP Part 2
Prompt
DCE long-case preparation: structured written reasoning for thunderclap headache and subarachnoid haemorrhage workup, giant cell arteritis urgent management, chronic migraine with medication overuse, and idiopathic intracranial hypertension diagnostic reasoning.

SAQ 1 — Headache with Red Flags: Differential, Investigation, and Management (20 marks, 30 minutes)

Prompt: Outline your systematic approach to this patient, including: (a) the SNNOOP10 red-flag screen and which red flags she has (4 marks); (b) your differential diagnosis and the single most likely diagnosis (4 marks); (c) the immediate investigations and their interpretation (5 marks); (d) the immediate management with exact drugs, doses, and rationale (4 marks); and (e) how this presentation differs from her usual migraine and why the difference matters (3 marks). [1]

Model Answer

(a) SNNOOP10 red-flag screen (4 marks): [1]

This patient has multiple red flags on the SNNOOP10 screen [1]. The relevant items are:

  • S — Systemic symptoms: She has fever (38.2 degrees), raised inflammatory markers (CRP 89, neutrophilic leucocytosis). This screens for infection, malignancy, and autoimmune disease — all of which are on the differential.
  • N — Neurologic deficit: She does not have a focal neurological deficit on examination, but the headache pattern has changed (see below).
  • O — Onset: The headache is not thunderclap (it developed over 3 days), so subarachnoid haemorrhage is less likely but not excluded.
  • P — Pattern change: This headache is different from her usual migraine — it is bifrontal rather than unilateral, progressive over days, associated with fever, and not relieved by her usual measures. Pattern change is a critical red flag requiring investigation.
  • (Positional and Precipitated by Valsalva): Not reported in this vignette.
  • (Papilloedema): Absent — fundoscopy is normal.

The presence of fever plus neck stiffness plus a changed headache pattern triggers investigation for a secondary cause. A primary headache diagnosis should not be accepted in a patient with systemic signs of infection. [1]

(b) Differential diagnosis and most likely diagnosis (4 marks): [1]

The differential for headache with fever and neck stiffness includes:

  1. Bacterial meningitis (most urgent) — S. pneumoniae, N. meningitidis, and (given her age over 50) Listeria monocytogenes
  2. Viral meningitis (enterovirus, HSV-2, VZV) — less likely given the marked neutrophilic leucocytosis and high CRP, but possible
  3. Encephalitis (HSV) — less likely as her GCS is 15 and there are no seizures or focal deficits, but must be considered
  4. Subarachnoid haemorrhage — less likely given the subacute onset over 3 days (SAH is typically thunderclap), but meningism can follow a small sentinel leak
  5. Cerebral abscess or parameningeal infection — particularly if there is a source (sinusitis, otitis media, dental infection)
  6. GCA-related headache with systemic inflammation — possible given her age (58), but GCA does not typically cause fever of 38.2 degrees and neck stiffness [1]

The single most likely diagnosis is acute community-acquired bacterial meningitis, given the fever, neck stiffness, raised inflammatory markers, and the neutrophilic leucocytosis. The changed headache pattern from her baseline migraine is the key — this is not her usual headache. [1]

(c) Immediate investigations and their interpretation (5 marks): [1]

  1. Blood cultures (two sets) before antibiotics — if possible without delaying therapy
  2. Lumbar puncture — if there are no contraindications on CT (and there are none — no mass, no shift). The CT is already normal, so LP can proceed. CSF should be sent for:
    • Cell count and differential, glucose (with a simultaneous serum glucose), protein, Gram stain, culture
    • Meningitis/encephalitis multiplex PCR panel (detects S. pneumoniae, N. meningitidis, H. influenzae, L. monocytogenes, C. neoformans, HSV-1/2, VZV, enterovirus)
    • Opening pressure should be measured
  3. Additional blood tests — coagulation profile, urea and electrolytes (for baseline before antibiotics and for SIADH monitoring), liver function, lactate
  4. HIV test — relevant if the CSF pattern is atypical or if opportunistic infection is suspected
  5. Consider temporal artery ultrasound — if CSF is negative and GCA remains in the differential, though the presentation favours infection [1]

The expected CSF pattern in bacterial meningitis is: elevated opening pressure, neutrophilic pleocytosis (typically hundreds to thousands of cells), low glucose (below 40 per cent of serum), high protein (above 1 g/L), and Gram stain positive for organisms. A lymphocytic pattern with normal glucose would suggest viral meningitis. [1]

(d) Immediate management with exact drugs, doses, and rationale (4 marks): [1]

The priority is to start empiric antibiotics immediately, without waiting for the LP result. The empiric regimen for suspected community-acquired bacterial meningitis in this patient (over 50, so at risk for Listeria) is: [1]

  • Ceftriaxone 2 g IV every 12 hours — covers S. pneumoniae and N. meningitidis
  • Vancomycin (loading dose 25-30 mg/kg, then adjusted to trough levels) — covers penicillin-resistant pneumococcus
  • Ampicillin 2 g IV every 4 hours — covers Listeria monocytogenes (intrinsically resistant to cephalosporins; critical in patients over 50, immunocompromised, pregnant, or alcoholic)
  • Dexamethasone 10 mg IV every 6 hours — given before or with the first antibiotic dose if pneumococcal meningitis is suspected; suppresses the inflammatory cascade from bacterial lysis [1]

If there is any clinical suggestion of encephalitis (altered mental status, seizures, focal neurology), add aciclovir 10 mg/kg IV every 8 hours until HSV PCR is negative. [1]

The rationale: antibiotics must not be delayed for LP or CT. The LP confirms the diagnosis and guides targeted therapy, but empiric therapy starts on suspicion. The ampicillin is essential because her age over 50 places her at risk for Listeria, which is not covered by ceftriaxone alone. [1]

(e) How this presentation differs from her usual migraine and why it matters (3 marks): [1]

Her usual migraine is unilateral, throbbing, lasts hours, occurs 2-3 days per month, and is controlled on propranolol. This presentation is different in every dimension: it is bifrontal (not unilateral), progressive over days (not hours), associated with fever and neck stiffness (not nausea and photophobia alone), and not relieved by her usual measures. This pattern change is a critical red flag (the P — Pattern change in SNNOOP10) and is the reason this patient requires investigation rather than assuming it is an atypical migraine. The principle: a headache that is different from a patient's established pattern, especially with systemic features, demands a search for a secondary cause. [1]


SAQ 2 — Chronic Migraine with Medication Overuse: Management Plan (10 marks)

Prompt: A 42-year-old woman has a 15-year history of migraine without aura. For the past year her headaches have been near-daily. She takes naproxen 500 mg twice daily on most days, a codeine-paracetamol combination tablet 3-4 times daily, and sumatriptan 50 mg on 3-4 days per week. She has tried propranolol (intolerant — bradycardia), topiramate (intolerant — cognitive side effects), and amitriptyline (intolerant — sedation). She is obese with a BMI of 33. Neurological examination is normal. Outline the integrated management plan. [1]

Model Answer

Diagnosis (2 marks): [1]

This patient has chronic migraine complicated by medication-overuse headache (MOH). The diagnosis of MOH is established by the ICHD-3 criteria: headache on 15 or more days per month in a patient with a pre-existing primary headache, with regular overuse of acute medication for 3 or more months. She exceeds the threshold on multiple fronts: simple analgesics (naproxen) on 15 or more days per month, a combination analgesic (codeine-paracetamol) on 10 or more days per month (the threshold for combination analgesics), and a triptan on 10 or more days per month (the threshold for triptans). She also has chronic migraine (headache on 15 or more days per month for more than 3 months, with migraine features on at least 8 days) [3].

The critical management principle: you cannot treat chronic migraine on top of medication overuse. The first step is always withdrawal. [1]

Step 1 — Withdraw the overused medications (3 marks): [1]

  • Naproxen and sumatriptan: Withdraw abruptly. Warn the patient that the headache will worsen for 1-2 weeks (the withdrawal headache) before improving.
  • Codeine-paracetamol combination: Withdraw by tapering over 2-4 weeks (codeine can cause physical dependence; abrupt withdrawal can cause opiate withdrawal symptoms — agitation, sweating, diarrhoea, insomnia).
  • Patient education: This is the most important step. The patient must understand that the medication she believes is helping is causing the daily headache. Expect resistance. Provide written information and follow-up. [1]

Step 2 — Start a preventive (3 marks): [1]

She has failed three oral preventives (propranolol, topiramate, amitriptyline) due to intolerance. The appropriate next step is a CGRP monoclonal antibody:

  • Erenumab 70-140 mg subcutaneously monthly (CGRP receptor antagonist; STRIVE trial evidence for episodic migraine)
  • Fremanezumab 225 mg subcutaneously monthly or 675 mg quarterly (CGRP ligand antibody; HALO-CM trial evidence for chronic migraine)
  • Galcanezumab 120 mg subcutaneously monthly after a 240 mg loading dose [1]

These agents have minimal systemic side effects (main adverse effect is injection-site reaction and constipation), do not cause weight gain (an advantage in this obese patient), and do not have the cognitive, cardiovascular, or sedation effects of the oral preventives she has failed. The AAN/AHS guideline (Silberstein 2012) established the oral preventives as Level A, but the CGRP monoclonal antibodies, developed subsequently, are now a standard option for patients who fail oral therapy [5].

Additional preventive options if CGRP monoclonal antibodies are not accessible or not funded: candesartan 8-16 mg daily, or onabotulinumtoxinA injections (155-195 units every 12 weeks), which is licensed for chronic migraine in many jurisdictions. [1]

Step 3 — Acute therapy for breakthrough migraine attacks and follow-up (2 marks): [1]

  • Provide a single acute therapy for breakthrough migraine attacks (e.g., rizatriptan 10 mg wafer), limited to a maximum of 2 days per week and never the overused drug class. A migraine diary is essential.
  • Address obesity — weight loss of 5-10 per cent can reduce migraine frequency and is a realistic goal with dietary and lifestyle intervention.
  • Follow up at 4-8 weeks after withdrawal to confirm resolution of MOH and assess preventive efficacy. Expect a significant reduction in headache frequency within 2 months of successful withdrawal. [1]

References

  1. [1]Do TP, Remmers A, Schytz HW, et al. Red and orange flags for secondary headaches in clinical practice: SNNOOP10 list Neurology, 2019.PMID 30587518
  2. [2]Perry JJ, Stiell IG, Sivilotti MLA, et al. Clinical decision rules to rule out subarachnoid hemorrhage for acute headache JAMA, 2013.PMID 24065011
  3. [3]Headache Classification Committee of the International Headache Society (IHS) Headache Classification Committee of the International Headache Society (IHS) The International Classification of Headache Disorders, 3rd edition Cephalalgia, 2018.PMID 29368949
  4. [4]Wall M, McDermott MP, Kieburtz KD, et al.; NORDIC Idiopathic Intracranial Hypertension Study Group Fibromyalgia: a clinical review JAMA, 2014.PMID 24737367
  5. [5]Silberstein SD, Holland S, Freitag F, Dodick DW, Argoff C, Ashman E Evidence-based guideline update: pharmacologic treatment for episodic migraine prevention in adults: report of the Quality Standards Subcommittee of the American Academy of Neurology and the American Headache Society Neurology, 2012.PMID 22529202