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Evidence-Based Supplement Research
Evidence-Based Supplement Research

Study Design

Type
Review
Population
children
Methods
systematic review of randomized controlled trials; searched PubMed, Cochrane Library, Semantic Scholar, and Google Scholar on October 15, 2024; five studies met criteria for qualitative synthesis
Acute cough and respiratory tract infections (RTIs), common in children, often lead to high antibiotic use. Echinacea, an herbal alternative, has been studied for its immune-modulating and antiviral effects to reduce the unnecessary use of antibiotics. This systematic review analyzed randomized controlled trials on Echinacea for pediatric acute cough and RTIs. PubMed, Cochrane Library, Semantic Scholar, and Google Scholar were searched on October 15, 2024. Five studies met all inclusion criteria and were retained for qualitative synthesis. The studies generally showed some concerns of bias in randomization and allocation concealment, as well as some issues about blinding and selective reporting. Grading of recommendations assessment, development, and evaluation assessment indicated high certainty of the reduction of symptom duration and antibiotic use, and moderate certainty for the prevention of infection. Evidence suggests that Echinacea purpurea, especially at higher doses (e.g., 2000 mg/day), may reduce RTI incidence, viral load, and symptom severity. Several trials have reported fewer antibiotic prescriptions and shorter fever duration, indicating public health benefits. Efficacy varied by formulation, extraction, and dosing, with tablet-based and hydroethanolic extracts showing more consistent results. Echinacea was well tolerated, only producing mild adverse effects of gastrointestinal discomfort and skin rashes. Some studies showed no significant difference from placebo, which underlines the need for standardized dosing and formulation. Overall, Echinacea may be a useful adjunct for pediatric RTI prevention and management, but further large, high-quality trials are needed to confirm optimal use, efficacy, and safety.

Research Insights

  • Grading of recommendations assessment, development, and evaluation assessment indicated high certainty of the reduction of symptom duration and antibiotic use

    Effect
    Beneficial
    Effect size
    Small
    Dose
    not stated
  • Grading of recommendations assessment, development, and evaluation assessment indicated high certainty of the reduction of symptom duration and antibiotic use

    Effect
    Beneficial
    Effect size
    Small
    Dose
    not stated
  • Several trials have reported fewer antibiotic prescriptions and shorter fever duration, indicating public health benefits.

    Effect
    Beneficial
    Effect size
    Small
  • and moderate certainty for the prevention of infection.

    Effect
    Neutral
    Effect size
    Small
    Dose
    2000 mg/day
  • and moderate certainty for the prevention of infection.

    Effect
    Neutral
    Effect size
    Small
    Dose
    2000 mg/day
  • Grading of recommendations assessment, development, and evaluation assessment indicated high certainty of the reduction of symptom duration and antibiotic use

    Effect
    Beneficial
    Effect size
    Small
  • Some studies showed no significant difference from placebo

    Effect
    Neutral
    Effect size
    Small
    Dose
    2000 mg/day
  • Some studies showed no significant difference from placebo

    Effect
    Neutral
    Effect size
    Small
    Dose
    2000 mg/day
  • Evidence suggests that Echinacea purpurea, especially at higher doses (e.g., 2000 mg/day), may reduce RTI incidence, viral load, and symptom severity.

    Effect
    Beneficial
    Effect size
    Moderate
    Dose
    2000 mg/day

Adverse Events Reported

  • Echinaceagastrointestinal discomfort

    Echinacea was well tolerated, only producing mild adverse effects of gastrointestinal discomfort and skin rashes.

    Finding
    Reported
    Grade
    mild
  • Echinaceaskin rashes

    Echinacea was well tolerated, only producing mild adverse effects of gastrointestinal discomfort and skin rashes.

    Finding
    Reported
    Grade
    mild
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