Atopic dermatitis (AD), a chronic and intensely
pruritic skin condition, affects an estimated 2% to 42% of children globally.
Beyond its visible skin lesions and intense itching, the condition carries a
significant risk of secondary infections that complicate clinical outcomes and
burden patients and caregivers alike.
A recent review highlights the critical link
between AD and increased susceptibility to a wide array of bacterial, viral,
and fungal infections—both cutaneous and systemic. This vulnerability stems
from several interrelated factors: a disrupted skin barrier, reduced
production of antimicrobial peptides, a dysregulated skin microbiome,
and a predominantly Th2-driven immune response. Together, these
abnormalities create a permissive environment for pathogen colonization and
invasion.
Among the most common culprits are Staphylococcus
aureus, which colonizes the skin of a majority of AD patients, and Malassezia
species, implicated in fungal overgrowths. These organisms not only
exacerbate eczematous inflammation but can also trigger systemic infections in
severe cases. The review emphasizes that during disease flare-ups, infections
should be considered key contributors—and in some cases, triggers—to worsening
symptoms.
Children with AD are more prone to frequent and
severe infections than their healthy counterparts, raising the urgency
for early identification and comprehensive management strategies. Recent
research underscores the importance of microbial surveillance and tailored
antimicrobial interventions in preventing complications.
The dual cornerstone of infection prevention in
AD lies in:
This growing body of evidence provides not only
a clearer understanding of the immunological and microbiological dynamics of AD
but also paves the way for more effective, individualized treatment approaches.
As research continues to evolve, integrating infection control into the broader
management of atopic dermatitis will be essential in improving outcomes and
quality of life for pediatric patients.
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