Active Infection & Immunity Lungs & Breathing

Discovering novel pneumonia phenotypes in Vietnamese patients using multimodal data and artificial intelligence

In plain English

AI plain-English summary

A Vietnamese patient with pneumonia is more likely to receive the wrong treatment because the risk scores and disease categories used to guide care were developed in Europe or North America, not in Ho Chi Minh City or Hanoi. This matters because community-acquired pneumonia and ventilator-associated pneumonia are the top reasons for hospital and ICU admission in low- and middle-income countries, yet almost all research on them comes from high-income settings. Doctors in Vietnam lack validated tools to predict which patients will need intensive respiratory support, or to decide who with suspected ventilator-associated pneumonia truly needs antibiotics. Without these tools, they either overtreat with antibiotics—fueling resistance—or undertreat, risking death. Over the past eight years, this team has built AI systems in Vietnam that analyse clinical data, medical images, and continuous physiological signals from custom monitoring platforms. They have already uncovered clinical and inflammatory patterns linked to outcomes in life-threatening infections. Now they will combine multimodal data with advanced pathogen detection and host immune profiling to identify new pneumonia phenotypes tied to the need for ICU respiratory support or antibiotic therapy. If successful, the research could produce risk scores and diagnostic strategies tailored to LMIC settings, reducing unnecessary antibiotic use and improving survival. It will also advance fundamental understanding of why some pneumonia patients deteriorate while others recover.

View original technical description
Community-acquired pneumonia (CAP) and ventilator-associated pneumonia (VAP) are respectively the most common indications for hospital and intensive care unit (ICU) treatment in low- and middle-income countries (LMICs). Yet most CAP and VAP research comes from high-income countries. Predicting severe CAP requiring ICU respiratory support (high-flow nasal oxygen or mechanical ventilation), and determining who with suspected VAP requires antibiotics, are critical decisions in LMICs. However, decision-making in LMICs is hindered by a lack of validated risk scores and limited knowledge of the underlying disease mechanisms. Over the last 8 years, our team have created artificial intelligence (AI) systems to analyse complex clinical, imaging and continuous physiological data acquired via custom-made platforms developed in Vietnam. In patients with life-threatening infections, we have discovered underlying clinical and inflammatory phenotypes linked to outcome, and pioneered advanced pathogen diagnostics. Our proposal builds on these foundations to create novel AI tools that will identify new phenotypes of CAP and VAP associated with the need for ICU respiratory support and antibiotic therapy respectively in LMICs. Combining multimodal clinical data and advanced pathogen identification with host response immune and inflammatory phenotyping we will also advance mechanistic understanding of these phenotypes that will inform new diagnostic and therapeutic strategies.

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Researchers

Catherine Thwaites (EPMC Awardee)David Clifton (EPMC Awardee)Hai Ho (EPMC Awardee)Julian Knight (EPMC Awardee)Le Van Tan (EPMC Awardee)Lei Clifton (EPMC Awardee)

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Original classification

Discovery Award

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