Epidemiological Trends of Hand, Foot, and Mouth Disease Across Three Distinct Periods in Jiangxi Province, China: A Retrospective Analysis from 2009 to 2022 - Scorecard - DentalSpire

Epidemiological Trends of Hand, Foot, and Mouth Disease Across Three Distinct Periods in Jiangxi Province, China: A Retrospective Analysis from 2009 to 2022

  • By

  • Jia Hu

  • Lihui Yu

  • Zijing Peng

  • Huanhong Pan

  • Yuan Jin

  • Zhili Zeng

  • Guanghui Xia

  • Yuan Wang

  • Zifen Li

  • Jianxiong Li

  • Yong Shi

  • Dajin Xiao

  • Haifeng Pan

  • Xiaoqing Liu

  • Tianchen Zhang

  • January 29, 2026

  • 0 min

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Clinical Scorecard: Epidemiological Trends of Hand, Foot, and Mouth Disease Across Three Distinct Periods in Jiangxi Province, China: A Retrospective Analysis from 2009 to 2022

At a Glance

CategoryDetail
ConditionHand, foot, and mouth disease (HFMD), a contagious viral illness primarily affecting children under 5 years
Key MechanismsCaused by enteroviruses including EV-A71, CVA16, CVA6; transmission dynamics influenced by viral transmissibility, spatiotemporal distribution, vaccination, and non-pharmacological interventions
Target PopulationChildren under 5 years, especially 1-year-olds with peak incidence and severity
Care SettingPublic health surveillance and clinical care in hospital and community settings

Key Highlights

  • HFMD is highly contagious with mostly mild symptoms but can cause severe complications including neurological and pulmonary manifestations.
  • The inactivated EV-A71 vaccine, introduced in China since 2016 for children aged 6 months to 5 years, shows high efficacy (97%) against EV-A71 associated HFMD.
  • Non-pharmacological interventions (NPIs) during COVID-19 (e.g., quarantine, distancing, masking) have impacted HFMD transmission dynamics.

Guideline-Based Recommendations

Diagnosis

  • Clinical diagnosis based on fever, vesicular rash on hands and feet, and oral ulcers.
  • Laboratory confirmation via RT-PCR testing for EV-A71, CVA16, and other enteroviruses, especially in severe or fatal cases.

Management

  • Supportive care for mild cases as most are self-limiting.
  • Close monitoring and early intervention for severe complications such as aseptic meningitis, encephalitis, and pulmonary edema.

Monitoring & Follow-up

  • Enhanced surveillance through national reporting systems.
  • Regular collection of clinical specimens from severe, fatal, and selected mild cases for pathogen identification.
  • Monitoring vaccination coverage rates and NPI stringency indices to assess impact on HFMD incidence.

Risks

  • Severe complications predominantly associated with EV-A71 infection in young children.
  • Limitations of EV-A71 vaccine include narrow protection spectrum and uncertain immunity duration.
  • Uneven vaccine coverage and potential resurgence without sustained public health interventions.

Patient & Prescribing Data

Children under 10 years, with focus on those aged 6 months to 5 years for vaccination

Two-dose inactivated EV-A71 vaccine schedule (28-day interval) initiated since 2016; real-world data show reduction in HFMD incidence, severity, and mortality post-vaccination

Clinical Best Practices

  • Implement EV-A71 vaccination programs targeting children aged 6 months to 5 years to reduce severe HFMD cases.
  • Maintain enhanced surveillance integrating clinical, laboratory, and vaccination data for timely outbreak detection and response.
  • Incorporate non-pharmacological interventions during outbreaks to mitigate transmission, especially in high-incidence regions.
  • Use epidemiological modeling and forecasting tools to guide public health strategies and resource allocation.

References

Original Source(s)

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