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Headache Approach: Primary Headaches vs Secondary Headaches (SNOOP4)

Writer: MaytaMayta

Updated: Jun 29, 2024

Primary vs. Secondary Headaches: A Clinical Guide

This table aims to assist physicians in differentiating between primary and secondary headaches, emphasizing the importance of recognizing "red flags" using the SNOOP4 mnemonic.

Feature

Primary Headache

Secondary Headache (SNOOP4)

Clinical Implications

Nature

Idiopathic (no identifiable underlying cause)

Symptomatic of an underlying medical condition

Important to determine if the headache is a symptom of a serious medical issue.

Severity

Can be severe, but generally not life-threatening

May be life-threatening

Urgent investigation and treatment may be required if the headache suggests a serious underlying cause.

SNOOP4

Not Present

Present

SNOOP4 factors indicate a higher likelihood of a secondary headache.

S: Systemic Symptoms

Absent

Fever, weight loss, HIV, cancer history (suggest meningitis, brain metastasis)

Evaluate for systemic infection, malignancy, or other underlying medical conditions.

N: Neurologic Symptoms

Absent

Confusion, weakness, seizures (indicate stroke, encephalitis)

Perform a thorough neurological examination and consider neuroimaging to rule out serious neurological conditions.

O: Onset Sudden

Gradual onset, often with predictable triggers

Sudden onset (thunderclap headache) suggests subarachnoid hemorrhage

Urgent neuroimaging (CT scan) is crucial to rule out SAH.

O: Older Age

Common in all age groups

New onset after 50 suggests giant cell arteritis

Consider giant cell arteritis, especially if temporal headache or jaw claudication is present.

P: Previous Headache History

Consistent pattern and severity

Change in pattern or severity suggests a secondary cause

Thorough history taking is crucial to identify any significant changes in headache characteristics.

P: Precipitating Factors

Common triggers (stress, fatigue, etc.)

Valsalva maneuver, exercise (suggest increased intracranial pressure)

Assess for triggers that may suggest increased intracranial pressure.

P: Positional

Headache pattern not significantly affected by position

Worse when lying down (suggests intracranial pressure changes)

Evaluate for positional changes that may indicate elevated intracranial pressure.

P: Papilledema

Absent

Present (indicates increased intracranial pressure)

Fundoscopic examination to assess for papilledema is essential.

Diagnosis

Clinical diagnosis based on ICHD-3 criteria

Requires further investigation to identify the underlying cause

Utilize appropriate diagnostic tests (neuroimaging, lumbar puncture, blood tests) based on suspected underlying conditions.

Management

Acute and preventive treatment focused on symptom relief and headache prevention

Treatment targets the underlying medical condition causing the headache

Address both the headache symptoms and the underlying medical condition.

Important Note: The presence of SNOOP4 factors warrants further investigation to rule out potentially life-threatening secondary headaches.



 

Introduction

Headaches are a ubiquitous symptom encountered in internal medicine practice, presenting various causes and clinical presentations. Differentiating between primary and secondary headaches is crucial for accurate diagnosis and effective management, particularly in identifying potentially life-threatening conditions. This article provides a comprehensive approach to headache evaluation and management, tailored for internal medicine residents.

 

I. Understanding Primary Headaches

Primary headaches are idiopathic, meaning they arise without a specific underlying medical condition. While they can significantly impact quality of life, they are generally not life-threatening. The three main types are:

  • Migraines: Characterized by unilateral, pulsating pain of moderate to severe intensity, often lasting 4-72 hours. Associated symptoms include nausea, vomiting, photophobia, and phonophobia.

    • Diagnosis: Based on clinical criteria outlined in the International Classification of Headache Disorders, 3rd edition (ICHD-3). Neuroimaging may be considered if red flags are present (see "Secondary Headaches").

    • Management:

      • Acute: NSAIDs (e.g., ibuprofen 600-1200 mg), triptans (e.g., sumatriptan 50-100 mg, max 200 mg/day), antiemetics (e.g., metoclopramide 10 mg IV).

      • Preventive: Beta-blockers (e.g., propranolol 80-240 mg/day), antiepileptics (e.g., topiramate 50-100 mg/day), antidepressants (e.g., amitriptyline 10-50 mg at bedtime).

  • Tension-type headache (TTH): Bilateral, pressing/tightening pain, typically mild to moderate in intensity, not worsened by physical activity.

    • Diagnosis: Primarily clinical, imaging rarely needed.

    • Management:

      • Acute: NSAIDs (e.g., ibuprofen 200-400 mg), acetaminophen (500-1000 mg).

      • Preventive: Tricyclic antidepressants (e.g., amitriptyline 10-75 mg at bedtime), stress management techniques.

  • Cluster Headache: Severe unilateral pain, often around the eye, associated with autonomic symptoms (lacrimation, rhinorrhea, ptosis).

    • Diagnosis: Clinical, but MRI may be considered to rule out secondary causes if atypical features are present.

    • Management:

      • Acute: High-flow oxygen (12-15 L/min via non-rebreather mask for 15-20 minutes), triptans (e.g., sumatriptan 6 mg SC).

      • Preventive: Verapamil (240-960 mg/day), lithium (600-900 mg/day), corticosteroids (short course during cluster periods).


 

II. Recognizing Secondary Headaches: The SNOOP4 Mnemonic

Secondary headaches are symptoms of an underlying medical condition, which can be serious and even life-threatening. The mnemonic "SNOOP4" helps identify red flags suggesting a secondary headache:

  • S: Systemic Symptoms: Fever, weight loss, HIV, cancer history (consider meningitis, brain metastasis).

  • N: Neurologic Symptoms: Confusion, weakness, seizures (consider stroke, encephalitis).

  • O: Onset Sudden: Thunderclap headache (consider subarachnoid hemorrhage).

  • O: Older Age: New onset headache after 50 (consider giant cell arteritis).

  • P: Previous Headache History: Change in pattern or severity (suggests a secondary cause).

  • P: Precipitating Factors: Valsalva maneuver, exercise (suggest increased intracranial pressure).

  • P: Positional: Worse when lying down (suggests intracranial pressure changes).

  • P: Papilledema: Indicates increased intracranial pressure.


 

III. A Detailed Diagnostic Approach

  • History and Physical Examination:

    • History: Detailed information on onset, duration, location, character, associated symptoms, and triggers.

    • Physical Exam: Thorough neurological exam, including vital signs, head and neck examination, and signs of increased intracranial pressure or focal neurological deficits.

  • Investigations:

    • Neuroimaging:

      • Non-Contrast CT (NCCT): First-line for suspected intracranial hemorrhage.

      • MRI: Preferred for detecting tumors, infections, and other structural abnormalities.

    • Lumbar Puncture (LP): Considered for suspected meningitis or SAH if initial CT is negative.

    • Blood Tests:

      • CBC: Infection or hematologic disorders.

      • Electrolytes, Liver and Renal Function Tests: Metabolic disturbances.

      • ESR and CRP: Elevated in giant cell arteritis.

      • Blood Cultures: If systemic infection is suspected.

 

IV. Management of Secondary Headaches

  • Meningitis:

    • Empirical Antibiotics: After blood cultures, start ceftriaxone (2 g IV every 12 hours) plus vancomycin (15-20 mg/kg IV every 8-12 hours). Add ampicillin (2 g IV every 4 hours) if Listeria is suspected.

    • Supportive Care: IV fluids, antipyretics, and seizure prophylaxis if indicated.

  • Subarachnoid Hemorrhage (SAH):

    • Initial Management: Stabilize airway, breathing, circulation. Manage blood pressure with IV labetalol or nicardipine to maintain SBP < 140 mmHg.

    • Definitive Treatment: Neurosurgical consultation for aneurysm clipping or endovascular coiling.

  • Giant Cell Arteritis:

    • High-Dose Corticosteroids: Prednisone 60-80 mg/day immediately to prevent vision loss. Temporal artery biopsy for confirmation.

    • Adjunct Therapy: Aspirin 81 mg daily to reduce ischemic complications.

  • Intracranial Pressure (ICP) Management:

    • Elevate Head of Bed (HOB): 30 degrees to facilitate venous drainage.

    • Mannitol or Hypertonic Saline: Mannitol (0.25-1 g/kg IV) or 3% saline for osmotic diuresis.

    • Definitive Treatment: Surgical intervention for mass lesions or hydrocephalus.

 

V. Conclusion

The approach to headache evaluation and management in a clinical setting requires a thorough understanding of both primary and secondary causes. Residents should prioritize identifying red flags, conducting appropriate diagnostic investigations, and initiating evidence-based treatments promptly to ensure optimal patient outcomes. Ongoing education and adherence to updated clinical guidelines are essential for maintaining high standards of care in headache management.

Key Take-Aways for Internal Medicine Residents:

  • Use the SNOOP4 mnemonic to quickly identify potential secondary headaches.

  • Remember that a thorough history and physical examination are essential for accurate diagnosis.

  • Don't hesitate to order appropriate investigations to rule out serious underlying conditions.

  • Recognize the urgency of treating secondary headaches to prevent potential complications.

  • Stay informed about the latest evidence-based guidelines for headache management.

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Message for International Readers
Understanding My Medical Context in Thailand

By Uniqcret, M.D.
 

Dear readers,
 

My name is Uniqcret, which is my pen name used in all my medical writings. I am a Doctor of Medicine trained and currently practicing in Thailand, a developing country in Southeast Asia.
 

The medical training environment in Thailand is vastly different from that of Western countries. Our education system heavily emphasizes rote memorization—those who excel are often seen as "walking encyclopedias." Unfortunately, those who question, critically analyze, or solve problems efficiently may sometimes be overlooked, despite having exceptional clinical thinking skills.
 

One key difference is in patient access. In Thailand, patients can walk directly into tertiary care centers without going through a referral system or primary care gatekeeping. This creates an intense clinical workload for doctors and trainees alike. From the age of 20, I was already seeing real patients, performing procedures, and assisting in operations—not in simulations, but in live clinical situations. Long work hours, sometimes exceeding 48 hours without sleep, are considered normal for young doctors here.
 

Many of the insights I share are based on first-hand experiences, feedback from attending physicians, and real clinical practice. In our culture, teaching often involves intense feedback—what we call "โดนซอย" (being sliced). While this may seem harsh, it pushes us to grow stronger, think faster, and become more capable under pressure. You could say our motto is “no pain, no gain.”
 

Please be aware that while my articles may contain clinically accurate insights, they are not always suitable as direct references for academic papers, as some content is generated through AI support based on my knowledge and clinical exposure. If you wish to use the content for academic or clinical reference, I strongly recommend cross-verifying it with high-quality sources or databases. You may even copy sections of my articles into AI tools or search engines to find original sources for further reading.
 

I believe that my knowledge—built from real clinical experience in a high-intensity, under-resourced healthcare system—can offer valuable perspectives that are hard to find in textbooks. Whether you're a student, clinician, or educator, I hope my content adds insight and value to your journey.
 

With respect and solidarity,

Uniqcret, M.D.

Physician | Educator | Writer
Thailand

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