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Safe Care for Every Newborn and Child, By Fay Allen, Innovation Specialist

11 September 2025

Patient safety is close to my heart; it’s fundamentally about preventing unintended harm when people are at their most vulnerable. In my role as an Innovation Specialist, I’m particularly focused on how new technologies can support this mission, especially when it comes to caring for our youngest patients.

Fay Allen, Innovation Specialist, NHS Supply Chain
World Patient Safety Day logo
Fay Allen RN, MSc, BSc, DipHE.

This year, the World Health Organisation’s theme for World Patient Safety Day is – ‘Safe care for every newborn and every child.

This resonates deeply with me. I believe we must not only raise global awareness about safety risks in neonatal and paediatric care but also champion research that can drive meaningful change. 

As also mentioned in the recently published Dash Report, patient safety for vulnerable populations like newborns and children can be enhanced by ensuring we accommodate innovative solutions that streamline and expedited diagnostic processes that ensure timely and effective treatment.

Medical Technology Innovation Dynamic Purchasing System

One initiative that I’m proud to support is our Dynamic Purchasing System (DPS), which was launched in January 2024. This approach helps ensure that innovative products can reach NHS patients quickly, exactly where they’re needed most.

A compelling example of this innovation in practice is the Genedrive MT-RNR1 ID Kit – a rapid, point-of-care genetic test that uses a simple mouth swab from a newborn to help clinicians select the safest and most appropriate antibiotic treatment for neonatal infections.

The challenge of getting the treatment right

The NICE guidelines recommend prompt treatment for suspected early-onset infections, typically with benzylpenicillin and gentamicin. However, there’s a significant patient safety risk that not everyone is aware of.

Some babies have a genetic variant known as MT-RNR1 m.1555A>G. If they receive gentamicin, they face a much higher risk of ototoxicity, which is irreversible hearing loss due to damage in the inner ear. This variant is more common in some ethnic backgrounds:

  • 1.81% in East Asian families.
  • 0.3% in Sub-Saharan African families.
  • Around 0.1% in other populations.

Until recently, genetic testing for this variant took too long to be useful in emergency neonatal care. But the Genedrive test now provides results in just 26 minutes, fast enough to guide immediate treatment decisions.  

The 10-year NHS plan supports this accelerated approach, with a focus on implementation of advanced technologies to improve patient safety, allowing for rapid diagnosis and intervention, ultimately safeguarding our youngest patients.

It’s incredible to see how this kind of rapid testing can make such a profound difference not just for a baby’s health, but for their future.

In conclusion, I believe innovations like the Genedrive test are essential tools in our mission to protect every newborn and child. By harnessing the power of technology, we can make sure that patient safety is at the forefront of neonatal care right from the very first moments of life.

Find out more: register for our webinar!

Fay Allen - presenter headshot

Unlocking the Potential of Breakthrough Diagnostic Tests

  • Date: Friday 26 September 2025
  • Time: 1pm – 2pm

This session will explore two disruptive point-of-care and pathology technologies launched under the Medical Technology Innovation DPS:

  • Genedrive MT-RNR1 – Point-of-care test for neonatal sepsis treatment (NICE HTE6).
  • Genedrive CYP2C19 – Genotype testing to optimise stroke patient treatment (NICE DG59).

Who should attend:
Consultants, midwives, nurses, members of the Clinical Procurement Specialist Network (CPSN), and procurement colleagues working in neonates and maternity, stroke and vascular, plastic surgery, or point of care / pathology.

Register today to reserve your spot on the webinar

After registering, you will receive a confirmation email with details on how to join.