Shingles (herpes zoster) is a dermatomal rash with painful blistering that is caused by the reactivation of the varicella-zoster virus (VZV). The initial infection with VZV usually occurs early in life, presenting as chickenpox (varicella), after which the virus remains dormant in the dorsal root ganglia. Immunocompromised individuals are at increased risk of VZV reactivation. Shingles is generally a clinical diagnosis, although further testing (e.g., PCR) may be indicated in unclear cases. Treatment with antiviral drugs, such as acyclovir, is usually effective. Potential complications include encephalitis and, particularly in the elderly population, painful postherpetic neuralgia. VZV may also affect the cranial nerves. Involvement of the trigeminal nerve may cause visual impairment up to blindness (herpes zoster opthalmicus), while involvement of the facial and vestibulocochlear nerves can cause facial paralysis and hearing loss (herpes zoster oticus). These presentations, in particular, require urgent medical attention to prevent serious complications. The recombinant zoster vaccine is recommended for the prevention of herpes zoster in all individuals ≥ 50 years of age and immunocompromised individuals ≥ 19 years of age.
- Causative pathogen: varicella-zoster virus (VZV)
- Transmission: via respiratory droplets and direct contact with VZV-infected vesicular fluid, causing chickenpox in those infected
- Risk factors for VZV reactivation: Reactivation typically occurs in immunocompromised individuals.
- Primary infection (chickenpox): respiratory transmission → VZV inoculates the lymphoid tissue of the nasopharynx and, subsequently, regional lymphoid tissue → viremia and chickenpox → recovery from chickenpox, but virus remains dormant in dorsal root ganglia (unless reactivated → recurrent infection)
- Reactivation (shingles): VZV reactivated, often many years after the primary infection (e.g., especially in immunocompromised individuals) → virus replicates in the dorsal root ganglia → travels through peripheral sensory nerves to the skin → shingles (less contagious than primary infection) 
Main symptoms: dermatomal distribution, typically affecting 1–3 dermatomes on one side of the body (most commonly affects the cervical, trigeminal, thoracic, and lumbar dermatomes) ; 
- The most frequent symptom and may precede the rash
- Usually described as “burning”, “throbbing”, or “stabbing”
- may occur.
- Erythematous maculopapular rash that quickly evolves into vesicular lesions 
- Pain 
- Additional symptoms 
Disseminated herpes zoster
- Herpes zoster characterized by > 20 extradermatomal lesions, involvement of ≥ 3 dermatomes, and/or visceral organ involvement 
- Typically seen in immunocompromised patients
Atypical presentation: may be seen in immunocompromised individuals
- No rash
- Recurrent herpes zoster
- Disseminated zoster
Subtypes and variants
Herpes zoster ophthalmicus (HZO) 
- Definition: reactivation of VZV in the ophthalmic division of the trigeminal nerve
- Epidemiology: occurs in 10–20% of herpes zoster cases 
Clinical features 
- Fever and skin symptoms as in shingles (see “Clinical features” above)
- Involvement of the ophthalmic nerve: reduced corneal sensitivity with severe pain in the innervated regions (forehead, bridge and tip of the nose)
- Involvement of the nasociliary nerve:
- Consult an ophthalmologist urgently, as HZO is a vision-threatening condition.
- Start .
- Consider IV antiviral therapy for immunocompromised patients or those with retinal involvement.
- Topical treatment may be added depending on the presentation. 
- Consider oral analgesia and lubricating eye drops to help manage pain.
- See also “HZO in patients with HIV. ” for the management of
- Can result in blindness, if not treated properly
Herpes zoster oticus 
- Definition: reactivation of VZV in the geniculate ganglion, affecting the seventh (facial) and eighth (vestibulocochlear) cranial nerves (also known as Ramsay Hunt syndrome)
- Epidemiology: occurs in 0.3–18% of patients
- Clinical features
- Diagnosis: tone audiometry
Clinical presentation is usually sufficient for a diagnosis. 
- PCR of VZV DNA 
Additional tests to consider 
- Serologic assay of VZV (IgM and IgG): can be used to identify active or passive immunity and diagnose primary VZV infection 
- Direct fluorescent antibody (DFA) of skin scrapings: not routinely recommended because it has a low sensitivity
- Tzanck test of skin vesicles
- Patients with recurrent herpes zoster infection or disseminated zoster: Consider evaluation for underlying malignancies, immunosuppression, or other causes (e.g., herpes simplex).
- Rash onset < 72 hours
Rash onset ≥ 72 hours
- New vesicles continually appearing: same treatment as for rash onset < 72 hours
- No new vesicles
- Consider supportive care alone for patients with uncomplicated disease.
- Consider ≥ 50 years, with , or evidence of complications (e.g., , neurological involvement). in patients aged
- Supportive care
- Infection control measures 
- Disposition: See “Admission criteria and consultations.”
Patients seeking care for suspected shingles should be placed on both VZV-naive or immunocompromised individuals) until all lesions have crusted over.  and to prevent transmission to other at-risk individuals (e.g.,
Antiviral therapy for herpes zoster 
Antiviral therapy speeds up the resolution of lesions, reduces viral shedding, reduces the formation of new lesions, and decreases pain. It is most effective if administered within approx. 72 hours or while new lesions are erupting.
- Indications 
- Regimens 
Anti-inflammatory and analgesic therapy 
- Consider prescribing medication regularly (e.g., every 6 hours) rather than as needed.
- Reassess frequently to ensure adequate analgesia and consider using standardized scales to monitor pain.
- For patients requiring opioid analgesia: Change to long-acting formulations once an effective dose is reached.
- For refractory or severe pain: Consider referral to a pain specialist for possible neural blockade. 
- For mild pain, consider one or more of the following: 
- For moderate to severe pain, add one of the following: 
- Consider adjuvant corticosteroids in patients with:
Admission criteria and consultations 
- Consider hospitalization if:
- The patient is immunocompromised
- Symptoms are atypical and/or severe (e.g., refractory or severe pain and rash, involvement of more than two dermatomes, disseminated zoster)
- There are complications (e.g., signs of myelitis, meningoencephalitis, ophthalmic involvement, or severe bacterial superinfection)
- Consider the following specialist consultations:
- Initiate antiviral therapy.
- Pain management and supportive care
- Consider adjunctive corticosteroids.
- Admit to the hospital and administer IV antivirals if there are signs of complicated herpes zoster, immunocompromised state, or disseminated zoster.
- Consider specialist consultation.
- Immunization with zoster vaccine
Postherpetic neuralgia 
- Definition: chronic neuropathic pain persisting for at least three months in the area previously affected by the rash
- Most common complication (occurs in 10–20% of overall herpes zoster cases)
- Strong association with age 
- Risk factors 
- Clinical features 
- The initial choice of analgesics should be guided by side-effect profiles, the potential for drug interactions, and patient comorbidities.
- One of the following tricyclic antidepressants: 
- One of the following anticonvulsants: 
- Topical treatments 
- Capsaicin patch or cream 
- Lidocaine patch 
- Opioids 
- Interventional pain therapy: Consider intrathecal glucocorticoid injections and/or neural blockade for severe cases.
- Prognosis: Pain typically continues to decrease over the first year but may last for months to years. 
Herpes zoster encephalitis 
- Risk factors 
- Clinical features 
- Treatment 
Additional complications 
- Cranial nerve involvement: Facial nerve palsy
- CNS involvement
We list the most important complications. The selection is not exhaustive.
Shingles vaccination 
- General principles
- Special considerations
Screening for shingles vaccination.  is not routinely required prior to