Risk factors for critical disease and death from hand, foot and mouth disease

Yilin He1, Jianguo Yang, Guang Zeng

  • 1From the *Taizhou Center for Disease Control and Prevention, Jiangsu Province, Taizhou; †Chinese Field Epidemiology Training Program, Chinese Center for Disease Control and Prevention, Beijing, China; ‡U.S. Centers for Disease Control and Prevention, Atlanta, GA; and §Chongqing Center for Disease Control and Prevention, Chongqing, China.

Insights

Glucocorticoids may worsen severe hand, foot, and mouth disease (HFMD), while andrographolides show protective effects. Early treatment with andrographolides could be beneficial for HFMD patients.

Area of Science:

  • Infectious Diseases
  • Virology
  • Clinical Pharmacology

Background:

  • Hand, foot, and mouth disease (HFMD) presents a significant public health concern in China.
  • High mortality and morbidity rates are observed in critical HFMD cases.
  • The underlying causes of severe and fatal HFMD remain largely undetermined.

Purpose of the Study:

  • To investigate the association between drug use and the development of critical illness and death in HFMD patients.
  • To identify potential therapeutic interventions for severe HFMD.

Main Methods:

  • A case-control study design was employed.
  • The study assessed the impact of specific drug treatments on HFMD outcomes.
  • Data analysis focused on comparing outcomes between treated and untreated patient groups.

Main Results:

  • Glucocorticoid treatment was linked to an increased incidence of severe HFMD.
  • Andrographolides demonstrated a protective effect against severe HFMD.
  • The protective effect of andrographolides was observed when administered within 48 hours of symptom onset or prior to critical diagnosis.

Conclusions:

  • Glucocorticoids are not recommended for treating mild HFMD due to potential adverse effects.
  • Andrographolides show promise for HFMD treatment and warrant further clinical investigation.
  • Clinical trials are recommended to evaluate andrographolides for enterovirus 71 infections.
Abstract

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