Varicella Rash Characteristics and Management
Rash Distribution and Appearance
Varicella presents with a characteristic centrifugal distribution pattern, beginning on the face and trunk and spreading to the extremities, with lesions appearing simultaneously in different stages of development (macules, papules, vesicles, and crusts) creating a distinctive "starry sky" appearance. 1
Classic Distribution Pattern
- Lesions typically begin on the face and trunk as the initial sites of presentation 1
- Progression is centrifugal: from the center (face/trunk) to the periphery (extremities) 1
- The scalp is frequently involved as part of the facial/cephalic distribution 1
- Unlike smallpox, varicella shows lesions simultaneously in different stages of progression in all affected areas 1
Lesion Evolution
- Lesions appear as erythematous macules that rapidly evolve to papules, then vesicles 1
- The typical rash consists of 250-500 lesions in immunocompetent patients 2
- The disease is usually self-limited, lasting 4-5 days and is characterized by fever, malaise, and the generalized vesicular rash 2
Atypical Presentations
- Varicella may have a modified presentation in areas of skin irritation such as sun exposure, pre-existing inflammation, diaper irritation, operative sites, burns, insect bites, or pre-existing skin disease 3
- In these cases, the rash may be monomorphic and without the typical "starry sky" appearance 3
High-Risk Populations and Complications
Immunocompromised Patients
- Infants, adolescents, adults, and immunocompromised persons are at higher risk for complications 2
- In immunosuppressed hosts, lesions can continue to develop for longer periods (7-14 days or more) 1
- These patients may develop more severe disease with cutaneous dissemination and visceral involvement including viral pneumonia, encephalitis, and hepatitis 4
Pregnant Women and Neonates
- Primary VZV infection in the final 3 weeks of pregnancy may cause transplacental infection and neonatal varicella 5
- Infants are most at risk of severe disease if born from 5 days before to 2 days after onset of the maternal varicella rash 5
- Strict isolation of pregnant women, neonates, and other immunocompromised individuals is mandatory 1
Treatment Approach
Immunocompromised Patients
High-dose intravenous acyclovir is the treatment of choice for VZV infections in immunocompromised hosts. 1, 6
- Dosing for varicella-zoster in immunocompromised patients:
- Treatment should be continued until clinical response is achieved, then switched to oral acyclovir or valacyclovir to complete 14-21 days of total treatment 1
- Each dose must be infused at a constant rate over 1 hour; rapid or bolus injection must be avoided 6
Neonatal Varicella
- Neonates (birth to 3 months): 10 mg/kg IV every 8 hours for 10 days 6
- Doses of 15-20 mg/kg have been used in neonatal herpes simplex infections, though safety and efficacy for these higher doses are not fully established 6
- Administration of varicella zoster immunoglobulin for post-exposure prophylaxis is advised for neonates at highest risk 5
Immunocompetent Patients
- Severe initial episodes in immunocompetent adults and adolescents: 5 mg/kg IV every 8 hours for 5 days 6
- The vast majority of immunocompetent persons require only symptomatic therapy directed toward reduction of fever and avoiding secondary bacterial skin infection 4
Infection Control
Contagious Period
- The patient remains contagious until all lesions are completely crusted over or no new lesions appear in 24 hours 1
- Peak viral titers occur in the first 24 hours after lesion onset, with progressive decline as lesions convert to crusts 7
- The typical duration of disease is approximately 2 weeks in immunocompetent hosts 1
Prevention
- Postexposure vaccination is effective in preventing illness or modifying varicella severity if used within 3 days, and possibly up to 5 days, of exposure 2
- If exposure does not cause infection, postexposure vaccination should induce protection against subsequent exposure 2
Critical Pitfalls to Avoid
- Do not delay treatment in immunocompromised patients or neonates—initiate IV acyclovir immediately upon clinical suspicion 1
- Do not use rapid or bolus IV injection of acyclovir; this can cause renal toxicity 6
- Do not discontinue isolation precautions until all lesions are fully crusted 1
- Do not miss atypical presentations in areas of pre-existing skin inflammation, which may lack the classic "starry sky" appearance 3
- Adjust acyclovir dosing for renal impairment: patients with creatinine clearance <50 mL/min require dosing interval adjustments 6