Can you write a detailed SOAP note for an 84-year-old woman with herpes zoster involving the right scalp, right V1/V2 facial distribution down to the cheek, with no optic nerve involvement?

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SOAP Note: 84-Year-Old Female with Herpes Zoster (Shingles)

Subjective

Chief Complaint:

  • Painful vesicular rash on right scalp and right side of face extending to cheek 1

History of Present Illness:

  • Patient reports prodromal pain that likely preceded the rash by 24-72 hours, characterized by burning, tingling, or paresthesia in the affected dermatome 2
  • Vesicular eruption developed in a unilateral dermatomal distribution involving the right V1/V2 trigeminal distribution 1, 2
  • Lesions progressed from erythematous macules to papules and then to vesicles, with possible coalescence 3
  • Duration of symptoms should be documented to determine if within the 72-hour window for optimal antiviral efficacy 1
  • Severity of acute pain should be quantified using a pain scale 4

Past Medical History:

  • Document any immunocompromising conditions including diabetes mellitus, malignancy, HIV/AIDS, rheumatoid arthritis, systemic lupus erythematosus, inflammatory bowel disease, or cardiovascular disease 5
  • Current medications, particularly immunosuppressive agents (corticosteroids >40mg daily, biologics, JAK inhibitors, chemotherapy) 1
  • History of varicella (chickenpox) infection or varicella vaccination 5
  • Prior herpes zoster episodes 5
  • Vaccination history, specifically recombinant zoster vaccine (Shingrix) status 1

Review of Systems:

  • Ophthalmic: No eye pain, vision changes, or photophobia (optic nerve unaffected per presentation) 6
  • Constitutional: Fever, malaise, or weight loss suggesting disseminated disease 1
  • Neurologic: Headache, confusion, or focal neurologic deficits suggesting CNS involvement 1
  • Respiratory: Cough or dyspnea suggesting pulmonary involvement 1
  • Gastrointestinal: Abdominal pain or elevated liver enzymes suggesting hepatic involvement 1

Objective

Vital Signs:

  • Temperature, blood pressure, heart rate, respiratory rate, oxygen saturation 1

Physical Examination:

Dermatologic:

  • Distribution: Unilateral vesicular eruption in right V1/V2 dermatomal distribution involving right scalp and right side of face extending to cheek 1, 2
  • Lesion characteristics: Thin-walled vesicles on erythematous base, possible pustules or early ulceration, assess for coalescence 3, 2
  • Stage of lesions: Document if lesions are still erupting (typically 4-6 days in immunocompetent hosts) or if any have begun to crust 3, 2
  • Assess for dissemination: Examine for lesions in >3 dermatomes, which would indicate disseminated disease requiring IV therapy 1
  • Hutchinson sign: Examine nasal tip for vesicles, which indicates nasociliary nerve involvement and higher risk of ocular complications 6

Ophthalmologic:

  • Visual acuity: Document baseline vision in both eyes 6
  • External examination: Eyelid edema, vesicles on eyelid margins, conjunctival injection 5, 6
  • Corneal examination: Punctate keratitis, pseudodendritic lesions (requires slit lamp by ophthalmology) 5
  • Pupillary response: Assess for afferent pupillary defect 6
  • Intraocular pressure: Elevated IOP suggests uveitis or trabeculitis 5
  • Given facial/V1 involvement, urgent ophthalmology consultation is mandatory even without current symptoms 1, 6

Lymphatic:

  • Palpable preauricular or cervical lymphadenopathy 5

Neurologic:

  • Cranial nerve examination, particularly CN V sensory function 6
  • Mental status if concern for encephalitis 1

General:

  • Assess for signs of immunocompromise or systemic illness 1

Assessment

Primary Diagnosis:

  • Herpes zoster (shingles) involving right V1/V2 trigeminal distribution 1, 2, 4

Risk Stratification:

  • Age 84 years: High risk for postherpetic neuralgia (PHN) and complications 5, 7
  • Facial involvement: Requires heightened vigilance for ophthalmic complications despite current lack of optic nerve involvement 1, 6
  • Immunocompetent vs. immunocompromised: Determine based on history and examination to guide therapy intensity 1, 3

Complications to Monitor:

  • Herpes zoster ophthalmicus with potential for keratitis, uveitis, retinitis, vision loss 5, 6
  • Postherpetic neuralgia (most common complication, risk increases with age) 5, 4, 7
  • Cranial nerve palsies 5
  • Secondary bacterial superinfection 5, 3
  • Disseminated disease (if immunocompromised) 1, 3

Plan

Immediate Management

1. Urgent Ophthalmology Referral:

  • Mandatory ophthalmology consultation within 24 hours due to V1 distribution involvement, regardless of current symptoms 1, 6
  • Risk of vision-threatening complications including keratitis, uveitis, and retinitis requires specialist evaluation 5, 6

2. Antiviral Therapy (Initiate Immediately):

For immunocompetent patient:

  • Valacyclovir 1000 mg orally three times daily for 7-10 days 1, 4
  • Alternative: Famciclovir 500 mg orally three times daily for 7-10 days 1, 4
  • Alternative: Acyclovir 800 mg orally five times daily for 7-10 days (requires more frequent dosing, less preferred) 1, 4
  • Treatment must be initiated within 72 hours of rash onset for optimal efficacy in reducing acute pain, accelerating lesion healing, and preventing PHN 1, 4
  • Continue treatment until ALL lesions have completely scabbed, not just for an arbitrary 7-day period 1

For immunocompromised patient or complicated disease:

  • Intravenous acyclovir 10 mg/kg every 8 hours 1, 3
  • Indications for IV therapy: disseminated disease (>3 dermatomes), severe immunosuppression, CNS complications, complicated ocular disease, or failure to respond to oral therapy within 7-10 days 1
  • Continue IV therapy for minimum 7-10 days and until clinical resolution (all lesions scabbed) 1
  • If immunocompromised, consider temporary reduction or discontinuation of immunosuppressive medications if clinically feasible 1

Renal dose adjustments:

  • Obtain baseline creatinine clearance 1
  • Valacyclovir: Adjust dose based on CrCl 1
  • Famciclovir: 500 mg q8h for CrCl ≥60; 500 mg q12h for CrCl 40-59; 500 mg q24h for CrCl 20-39; 250 mg q24h for CrCl <20 1
  • Monitor renal function weekly during IV acyclovir therapy 1

3. Pain Management:

Acute pain control:

  • Acetaminophen 650-1000 mg orally every 6 hours as needed 1
  • Ibuprofen 400-600 mg orally every 6-8 hours as needed (if no contraindications) 1
  • Topical ice or cold packs to affected area 1
  • For severe pain: Consider short-acting opioids (e.g., oxycodone 5-10 mg every 4-6 hours) 4
  • Avoid topical anesthetics as primary therapy (minimal benefit) 1

Adjunctive therapy for severe acute pain:

  • Consider gabapentin 300 mg orally three times daily, titrate as needed 4, 8
  • Consider pregabalin 75 mg orally twice daily, titrate as needed 4, 8
  • Corticosteroids (prednisone) may be considered as adjunctive therapy in select cases of severe, widespread disease, but carry significant risks in elderly patients 1
  • Avoid corticosteroids if immunocompromised due to risk of disseminated infection 1

4. Skin Care:

  • Keep lesions clean and dry 5
  • Avoid applying topical products to active vesicular lesions 1
  • Emollients may be used after lesions have crusted to prevent excessive dryness 1
  • Monitor for secondary bacterial infection (increased erythema, purulent drainage, warmth) 5, 3

5. Infection Control:

  • Patient must avoid contact with susceptible individuals (pregnant women, immunocompromised, unvaccinated individuals, neonates) until ALL lesions have crusted 1
  • Cover lesions with clothing or dressings to minimize transmission risk 1
  • Lesions are contagious to individuals who have not had chickenpox or vaccination 1

Laboratory Testing

Baseline studies:

  • Serum creatinine and calculated CrCl (for antiviral dosing) 1
  • Complete blood count (if concern for immunosuppression) 1
  • Glucose or HbA1c (diabetes screening, as HZ may unmask metabolic disease) 2

Confirmatory testing (if indicated):

  • PCR of vesicle fluid (most sensitive/specific, approaching 100%) - indicated if immunocompromised, atypical presentation, or diagnostic uncertainty 2, 4, 8
  • Direct immunofluorescence (DFA) antigen testing of vesicle fluid (rapid alternative to PCR) 2
  • Tzanck smear (bedside adjunct showing multinucleated giant cells, cannot differentiate VZV from HSV) 2, 4
  • Viral culture (less practical, longer turnaround) 2
  • Do NOT order VZV IgG/IgM serology (does not aid in acute diagnosis) 2

Additional screening:

  • Consider HIV testing if risk factors present or recurrent HZ 5, 2
  • Consider evaluation for occult malignancy if clinically indicated 5, 2

Monitoring and Follow-Up

Short-term monitoring:

  • Daily ophthalmology follow-up if any ocular symptoms develop (eye pain, vision changes, photophobia) 6
  • Reassess in 3-5 days to ensure lesions are responding to therapy 1
  • If lesions fail to begin resolving within 7-10 days, suspect acyclovir resistance and obtain viral culture with susceptibility testing 1
  • Monitor for signs of dissemination: new lesions in distant dermatomes, fever, respiratory symptoms, neurologic changes 1
  • Continue antiviral therapy until ALL lesions have completely scabbed 1

Treatment failure or resistance:

  • For confirmed acyclovir-resistant VZV: Foscarnet 40 mg/kg IV every 8 hours until clinical resolution 1
  • Acyclovir resistance is rare in immunocompetent patients but occurs in up to 7% of immunocompromised patients 1

Long-term monitoring:

  • Assess for development of postherpetic neuralgia (pain persisting >30 days after lesion healing) 4, 7
  • If PHN develops: Gabapentin, pregabalin, tricyclic antidepressants (amitriptyline, nortriptyline), or long-acting opioids are first-line treatments 4, 8
  • Topical lidocaine 5% patch or capsaicin cream as second-line agents for PHN 4, 8

Prevention of Future Episodes

Vaccination:

  • Strongly recommend recombinant zoster vaccine (Shingrix) after recovery from current episode 5, 1
  • Shingrix provides >90% efficacy in preventing future HZ episodes and is recommended for ALL adults ≥50 years regardless of prior HZ episodes 5, 1
  • Two-dose series: Second dose 2-6 months after first dose 5
  • Can be administered after recovery from acute HZ episode 5, 1

Patient Education

Disease course:

  • Explain that lesions typically continue to erupt for 4-6 days with total disease duration of approximately 2 weeks in immunocompetent hosts 3, 2
  • Emphasize importance of completing full antiviral course until all lesions scab 1
  • Discuss risk of postherpetic neuralgia, which increases with age (up to 50% in those >80 years) 5, 7

Warning signs requiring immediate return:

  • Eye pain, vision changes, or photophobia 6
  • New lesions in distant body areas (suggesting dissemination) 1
  • Fever, severe headache, confusion (suggesting CNS involvement) 1
  • Respiratory symptoms (suggesting pulmonary involvement) 1
  • Signs of secondary bacterial infection (increased redness, pus, warmth) 5, 3

Transmission precautions:

  • Avoid contact with pregnant women, immunocompromised individuals, unvaccinated persons, and neonates until all lesions crust 1
  • Cover lesions with clothing or dressings 1
  • Practice good hand hygiene 8

References

Guideline

Management of Herpes Zoster

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Herpes Zoster Clinical Presentation and Management

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Management of Herpes Zoster Reactivation in Individuals with Varicella Antibodies

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Herpes Zoster Ophthalmicus: A Review for the Internist.

The American journal of medicine, 2017

Research

Herpes zoster and postherpetic neuralgia.

Expert review of vaccines, 2010

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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