DeNTS: Clinical Decision Support in Non-typhoidal Salmonella Bloodstream Infections in Children
Study Details
Study Description
Brief Summary
In sub-Saharan Africa, non-typhoidal Salmonella (NTS) are a frequent cause of bloodstream infection, display high levels of antibiotic resistance and have a high case fatality rate (15%). In Kisantu hospital in the Democratic Republic of Congo (DR Congo), NTS account for 75% of bloodstream infection in children and many children are co-infected with Plasmodium falciparum (Pf) malaria. NTS bloodstream infection presents as a non-specific severe febrile illness, which challenges early diagnosis and, as a consequence, prompt and appropriate antibiotic treatment.Moreover, at the first level of care, frontline health workers have limited expertise and diagnostic skills and, as a consequence, clinical danger signs that indicate serious bacterial infections are often overlooked.
Basic handheld diagnostic instruments and point-of-care tests can help to reliably detect danger signs and improve triage, referral and the start of antibiotics, but there is need for field implementation and adoption to low-resource settings. Further, it is known that some clinical signs and symptoms are frequent in NTS bloodstream infections. The integration of these clinical signs and symptoms in a clinical decision support model can facilitate the diagnosis of NTS bloodstream infections and target antibiotic treatment.
The investigators aim to develop such a clinical decision support model based on data from children under five years old admitted to Kisantu district referral hospital in the Democratic republic of the Congo. While developing the model, the investigators will focus on the signs and symptoms that can differentiate NTS bloodstream infection from severe Pf malaria and on the clinical danger signs that can be assessed by handheld diagnostic instruments and point-of-care tests. The deliverable will be a clinical decision support model ready to integrate in an electronic decision support system.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| NTS bloodstream infection growth of NTS in blood culture |
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| NTS/Pf malaria co-infection concurrence of current Pf malaria infection and NTS bloodstream infection |
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| Other pathogen bloodstream infections growth of a pathogen other than NTS in blood culture |
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| Severe Pf malaria mono-infection defined according to WHO-criteria |
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| Other causes of febrile illness requiring hospital admission Current Pf malaria infection: see above Recent Pf malaria infection: see above Non-confirmed bloodstream infection without Pf malaria: no growth in blood culture and negative results in all Pf malaria tests If feasible, severe bacterial localized infections such as pneumonia, meningitis, osteomyelitis, complicated urinary tract infection, abscess, skin/soft tissue infection or abdominal infection, will be assessed and clinically defined |
Outcome Measures
Primary Outcome Measures
- Predictive signs and symptoms [12 months]
Identify clinical signs and symptoms predictive for and differentiate between: 1.1. NTS bloodstream infection 1.2. severe Pf malaria mono-infection 1.3. NTS/Pf malaria co-infection 1.4. other-pathogen bloodstream infections 1.5. other causes of febrile illness requiring hospital admission
- Contribution of handheld diagnostics and point-of-care tests to NTS bloodstream infection diagnosis [12 months]
Assess the contribution of handheld diagnostic instruments and point-of-care tests to the detection of danger signs associated with NTS bloodstream infection
- Clinical decision support model for NTS bloodstream infection [12 months]
Develop a clinical decision support model for diagnosis of NTS bloodstream infection based on the predictive clinical signs and symptoms associated with NTS bloodstream infections
Secondary Outcome Measures
- Contribution of handheld diagnostics and point-of-care tests to bloodstream infection diagnosis [12 months]
Assess the contribution of handheld diagnostic instruments and point-of-care tests to the detection of danger signs associated with all pathogen bloodstream infection (NTS and other-pathogen bloodstream infections combined)
- Clinical decision support model for bloodstream infection [12 months]
Develop a clinical decision support model for diagnosis of bloodstream infection caused by all pathogens (NTS and other pathogens combined)
- Case fatality [12 months]
Determine the clinical signs and symptoms associated with case fatality in NTS bloodstream infection and all pathogen bloodstream infections (NTS and other pathogen combined)
- Geographical clustering [12 months]
Assess the geographical clustering of cases with NTS bloodstream infection
Eligibility Criteria
Criteria
Inclusion Criteria:
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Be a child of > 28 days and < 5 years old
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Be admitted to Kisantu Hospital
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Having a blood cultured sampled according to the criteria for suspected bloodstream infection embedded in the blood culture surveillance, i.e. presence of objective fever, hypothermia or history of fever during past 48 hours + at least one of the following criteria:
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Hypotension, confusion or increased respiratory rate
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Suspicion of severe localized infection: pneumonia, meningitis, osteomyelitis, complicated urinary tract infection, abscess, skin/soft tissue infection or abdominal infection
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Suspicion of typhoid fever
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Suspicion of severe Pf malaria
- Having a caregiver willing and able to provide written informed consent
Exclusion Criteria:
- None
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Kisantu general referral hospital | Antwerp | Belgium | 2000 |
Sponsors and Collaborators
- Institute of Tropical Medicine, Belgium
- KU Leuven
- Institut National de Recherche Biomédicale. Kinshasa, République Démocratique du Congo
- Hôpital St. Luc Kisantu, République Democratique du Congo
- International Vaccine Institute
Investigators
- Principal Investigator: Bieke Tack, MD, Institute of Tropical Medicine
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- ID ITM202007