AI-Enabled Indoor Air Quality Monitoring for a U.S. Children's Hospital
A comprehensive trial test study
SensusAir Research Team · SensusAir
Published 09 Oct 2025 · 8 min read

Abstract
A trial of AI-driven indoor air quality monitoring in a paediatric hospital, tracking particulate matter, CO₂, volatile organic compounds and viral pathogens including RSV, COVID-19 and influenza. Viral spread and load remained within prescribed thresholds throughout, yet elevated VOC levels and high PM1 peaks point to targeted interventions still needed in a setting where the occupants are the most vulnerable.
Key findings
- CO₂ range
- 600–1,600 ppm
- VOC range
- 407–500 ppb
- Viral pathogens
- RSV, COVID-19, influenza
- Viral spread indicator
- Stable
Peaks concentrated at 1,200–1,400 ppm
Peaks indicating potential off-gassing
Identified via spectral analysis
Within prescribed thresholds
Introduction
Paediatric healthcare settings combine two conditions that make indoor air quality unusually consequential: occupants with developing respiratory systems and compromised immunity, and a building operating continuously with high turnover of people, cleaning chemistry and clinical consumables.
This trial evaluated whether continuous AI-interpreted monitoring could hold both threads at once, infection-relevant signals and chemical exposure, inside a working children's hospital.
Methodology
The study applied the same four-pronged approach used across the trial programme: data collection via sensor deployment, pattern recognition using the AI engine, near real-time reporting through dashboards, and risk assessment with mitigation recommendations.
Measured parameters were temperature, humidity, particulate matter (PM1, PM2.5, PM4, PM10 in µg/m³), carbon monoxide, CO₂ in ppm, VOCs, and viral pathogen detection through spectral signatures.
- Phase 1, telemetry collection establishing baseline metrics
- Phase 2, risk assessment analysing Viral Risk Index, Pathogen Risk Index and Vapour Pressure Deficit
- Phase 3, forensic analysis identifying contamination sources
Results: carbon dioxide
CO₂ ranged from 600 ppm to 1,600 ppm, with peaks concentrated between 1,200 and 1,400 ppm. The upper end of that range indicates periods where ventilation was not keeping pace with occupancy, relevant both to comfort and to the dilution of airborne infectious particles.
Results: particulate matter
As in the other facilities studied, coarse particle control performed well while the finest fraction, the fraction that reaches deepest into a child's lower airway, was the one showing excursions.
- PM1, high peaks detected
- PM2.5, elevated
- PM4 and PM10, within normal ranges
Results: volatile organic compounds
VOC concentrations ranged from 407 to 500 ppb, with peaks indicating potential off-gassing. In a clinical environment the likely contributors are disinfectant chemistry, consumables and furnishings, all of which are substitutable once identified.
Environmental KPIs
- Viral Spread Indicator, stable
- Pathogen Risk Indicator, normal
- IAQ Index, variable, with concerning fine particles and elevated VOCs
Limitations
- Single-facility study
- Specific VOC compounds not identified individually
- No evaluation of mitigation impact within the study window
- Seasonal and occupancy pattern analysis not undertaken
Conclusions and recommendations
The study establishes that the technology monitors paediatric healthcare environments effectively, distinguishing infection-relevant signals from chemical exposure in the same data stream.
- Expand sensor deployment across the estate
- Implement HEPA filtration
- Move to low-VOC disinfectants
- Enhance ventilation in zones showing CO₂ excursions
- Integrate real-time dashboards
- Run follow-up studies evaluating mitigation effectiveness
References
- 1.WHO. Global air quality guidelines (2021)
- 2.US EPA. Indoor air quality in healthcare settings
- 3.ASHRAE Standard 170. Ventilation of health care facilities
Take this further
Download the original document, or see how the same measurement approach applies to your estate.
Reproduced from the original publication page.