Skip to main content

Project details

Rapid testing of urinary tract infections

The UTI-Diag project is exploring whether point-of-care tests could improve detection and management of urinary tract infections (UTIs) and reduce the pressures driving antimicrobial resistance.

The challenge

Urinary tract infections (UTIs) are caused by a range of pathogens and are extremely common, with globally more than  400 million UTI cases each year. The prevalence of UTIs has been increasing over the past two decades, particularly in low- and middle-income countries.

In low-resource settings, treatment is typically syndromic, or diagnosis is made primarily on clinical signs, which is incorrect in about a third of cases. This leads to high levels of antibiotic use, driving the spread of antimicrobial resistance. Disease recurrence is common, for example, occurring in 26-44% of women treated for UTIs. 

UTI symptoms are not specific to infections, so the first challenge in clinical care is to determine as quickly as possible whether a patient actually has an infection. Clinical management could also be improved by knowledge about the antibiotic resistance profile of a pathogen, enabling a suitable treatment to be selected.

The project

The UTI-Diag project is exploring whether new diagnostic and sampling technologies could be applied to UTI management in sub-Saharan Africa to enable more targeted antibiotic use and reduce the pressure driving the emergence and spread of antimicrobial resistance.

The project is focusing on four tools that could improve UTI detection and patient care:

  • A simple sample collection and transport device, based on a card with disks for urine and blood samples, which can be sealed and sent by regular mail. This could be used by patients or clinicians.
  • A lateral flow test (ULTRiPLEX), which detects two urinary proteins associated with UTIs, is to be used in initial triage to determine whether patients have infections.
  • UTI-Diag, a battery-operated point-of-care device for molecular detection of antimicrobial resistance genes, to guide choice of antibiotic treatment.
  • An adapted version of the AviroPocketClinic digital tool, which reports the results, aids clinical decision-making, and has built-in communications and training support modules.

The project is carrying out clinical validation studies of these tools at multiple sites in Cameroon and Senegal. Special efforts are being made to investigate their use in marginalised and hard-to-reach communities so that the results are as generalisable as possible. The performance of the tools is being compared with that of multiple other strategies and detection methods. Costing analyses are also being carried out.

Impact

The UTI-Diag project will provide data on one of the most common infections, which, in addition to leading to many deaths, has a major impact on quality of life, places high demands on health systems, and is increasingly difficult to treat due to antibiotic resistance. It will:

  • Demonstrate whether the tools being tested, individually or collectively, can lead to more targeted treatment of UTIs.
  • Show whether their use improves patient outcomes and leads to more rational use of antibiotics.
  • Provide health authorities with information on the prevalence, spread and resistance patterns of infections.
  • Generate data on the feasibility of the tools and their costs to inform national decision-making.

The project estimates that, with widespread use of the tools, treatment failures, hospital admissions, and healthcare costs could be reduced by more than 40%, and misdiagnosis could be reduced from around 33% to 5%. This would deliver significant benefits to patients, health systems and the long-term battle against AMR.

Consortium map

Coordinator

Beneficiaries

MAA GLOBAL

Location
JOHANNESBURG, South Africa
EU contribution
€501 125,00
Total cost
€501 125,00

INSTITUT PASTEUR DE DAKAR

Location
Dakar, Senegal
EU contribution
€758 205,13
Total cost
€758 205,13

CAPITAINER AB

Location
SOLNA, Sweden
EU contribution
€349 736,25
Total cost
€349 736,25

PASTEUR NETWORK

Location
Paris, France
EU contribution
€75 000,00
Total cost
€75 000,00

Aviro Med Design Pty Ltd

Location
Cape Town, South Africa
EU contribution
€503 750,00
Total cost
€503 750,00

CENTRE PASTEUR CAMEROON

Location
YAOUNDE, Cameroon
EU contribution
€450 000,00
Total cost
€450 000,00

AIDIAN OY

Location
Espoo, Finland
EU contribution
€356 250,00
Total cost
€356 250,00

Partners

MOLOGIC LTD

Location
Bedford, United Kingdom

THE UNIVERSITY OF CUMBRIA LBG

Location
Carlisle, United Kingdom
Global Health EDCTP3-funded CECABI II project logo
  • In progress
  • Cross-disease or disease unspecific
Building research oversight capacity in Côte d’IvoireThe CECABI II project is developing the capacity of research ethics bodies in Côte d’Ivoire and enhancing coordination with its national...
Global Health EDCTP3-funded STRATEGIC project logo
  • In progress
  • Cross-disease or disease unspecific
Enhancing oversight of digital health technologyThe STRATEGIC project is developing the capacity of sub-Saharan African countries to regulate the use of digital tools in research and...
Global Health EDCTP3-funded BRIDGE NETWORK project logo
  • In progress
  • Cross-disease or disease unspecific
Building capacity in health data analysisThe BRIDGE NETWORK project is establishing five centres of excellence to build skills in the use of health data to address key health challenges in...