Driving Reduced AIDS-associated Meningo-encephalitis Mortality
NCT ID: NCT03226379
Last Updated: 2022-05-04
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
495 participants
INTERVENTIONAL
2016-04-23
2021-09-30
Brief Summary
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Detailed Description
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Cryptococcal meningitis alone is estimated to account for up to 20% of HIV-related mortality and its' incidence in Africa, unlike in resource-rich settings, has remained high despite antiretroviral roll out.
In African low and middle-income countries (LMICs) mortality associated with cryptococcal meningitis has been estimated at 70% at 3 months.
Tuberculous meningitis mortality also remains unacceptably high and is reported at over 70% in a study from Cameroon. Delays in diagnosis are key causes of poor patient outcomes for tuberculous and bacterial meningitis, and cryptococcal meningitis where patients present late and with advanced disease.
The aim of the DREAMM study is to drive down this unacceptably high mortality associated with HIV-associated meningo-encephalitis in LMICs.
A further aim is to provide capacity building in implementation research at each of the sites driven by the local African Principal Investigators (PIs) (Dr Cecilia Kanyama, Lilongwe, Malawi; Dr Charles Kouanfack, Yaoundé, Cameroon; Dr Sayoki Mfinanga, NIMR, Dar es Salaam Tanzania, Dr Saulos Nyirenda, Zomba, Malawi).
The project is in three phases:
1. Observation: Local clinical and laboratory procedures and practices and availability of essential drugs and diagnostic tests for routine care of HIV-associated meningo-encephalitis patients in three study countries will be observed and documented. 75 patients in total will be recruited into the observation phase of DREAMM, 25 patients from each study country.
2. Training: A co-designed laboratory and clinical training program on HIV-associated meningitis in LMICs tailored to frontline healthcare workers (HCWs) will be delivered. Key clinical and laboratory routine HCWs will be trained including on the latest point of care (POC) diagnostic tests and safe administration of essential medicines for HIV-associated meningo-encephalitis such as amphotericin B deoxycholate using a Train the Trainer approach. The knowledge and skills will be disseminated widely following this training by frontline HCWs. Locally adapted optimal clinical and laboratory pathways for the diagnosis and treatment of HIV-related meningoencephalitis in resource limited settings will be devised during the training phase using a health system engineering approach.
3. Implementation: Implementation of an algorithmic approach to diagnosis and treatment of HIV-associated meningitis including aggressive microbiological detection and treatment of cryptococcosis and tuberculosis in the five study sites. The aim is to reduce the time from participant presentation to diagnostic testing and administration of effective, microbiologically-driven treatment. As part of the implementation of the algorithm, the optimised clinical and laboratory pathways endorsed by local leadership are implemented. Communities of practice are formed with weekly multidisciplinary meetings to discuss clinical cases and continue laboratory capacity building.
The data from the observation and implementation phases of the study will be fed back to local ministries of health (MOH), and access to essential antifungal drugs and diagnostic tests for HIV-associated meningitis improved and finally, cohesive HIV-related meningitis guidelines for African LMICs developed.
Important sub-studies include a health economics evaluation study to determine the cost of the intervention and routine care costs. A new semi-quantitative cryptococcal antigen lateral flow assay (CrAg LFA) (CryptoPS, Biosynex, Strasburg, France) will be evaluated uniquely for the diagnosis of patients with meningo-encephalitis. New, POC polyvalent tests (CrAg/HIV) and (CrAg/Streptococcus pneumoniae) will also be evaluated.
These POC tests nested within algorithms, and the new tests being evaluated, together with administration of recommended, microbiologically driven treatments have the potential to significantly reduce CNS infection-related mortality by reducing delays in proven diagnosis and initiation of effective treatments.
Conditions
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Study Design
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NA
SEQUENTIAL
HEALTH_SERVICES_RESEARCH
NONE
Study Groups
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DREAMM
4 DREAMM interventions to reduce HIV-related meningoencephalitis mortality once access to essential diagnostic tests and medicines:
1. Health system strengthening
2. Delivery of a co-designed education program tailored to frontline healthcare workers
3. Implementation of an algorithm for HIV-related meningoencephalitis
4. Infectious diseases/AHD mentorship and laboratory capacity building
DREAMM
4 DREAMM interventions to reduce HIV-related meningoencephalitis mortality once access to essential diagnostic tests and medicines:
1. Health system strengthening
2. Delivery of a co-designed education program tailored to frontline healthcare workers
3. Implementation of an algorithm for HIV-related meningoencephalitis
4. Infectious diseases/AHD mentorship and laboratory capacity building
Interventions
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DREAMM
4 DREAMM interventions to reduce HIV-related meningoencephalitis mortality once access to essential diagnostic tests and medicines:
1. Health system strengthening
2. Delivery of a co-designed education program tailored to frontline healthcare workers
3. Implementation of an algorithm for HIV-related meningoencephalitis
4. Infectious diseases/AHD mentorship and laboratory capacity building
Eligibility Criteria
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Inclusion Criteria
2. Known to be HIV positive or willing to undertake an HIV test
3. Willing to agree to participate in the study
Exclusion Criteria
2. HIV negative patients
3. Pregnant or lactating patients
4. Patients presenting with a known diagnosis of primary CNS Lymphoma or cerebral malaria
5. COVID-19 infected patients
Patients who are HIV negative or are diagnosed with cerebral malaria on hospital admission or after initial investigation will be excluded or withdrawn from the DREAMM study.
18 Years
ALL
No
Sponsors
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European and Developing Countries Clinical Trials Partnership (EDCTP)
OTHER_GOV
National Agency for Research on AIDS and Viral Hepatitis (ANRS)
OTHER
Institut Pasteur
INDUSTRY
National Institute for Medical Research, Tanzania
OTHER_GOV
Amana Hospital, Dar es Salaam, Tanzania
UNKNOWN
University of North Carolina Project-Malawi (UNC Project), Lilongwe, Malawi
UNKNOWN
Kamuzu Central Hospital
OTHER
Yaounde Central Hospital
OTHER_GOV
Zomba Central Hospital, Zomba, Malawi
UNKNOWN
Lighthouse Trust
OTHER
Mwananyamala Hospital, Dar es Salaam, Tanzania
UNKNOWN
St George's, University of London
OTHER
Responsible Party
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Principal Investigators
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Angela Loyse, MD
Role: PRINCIPAL_INVESTIGATOR
St George's, University of London
Locations
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Hôpital Central Yaoundé
Yaoundé, , Cameroon
Kamuzu Central Hospital
Lilongwe, , Malawi
Zomba Central Hospital
Zomba, , Malawi
Amana Hospital
Dar es Salaam, , Tanzania
Mwananyamala Hospital
Dar es Salaam, , Tanzania
Countries
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References
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Mfinanga S, Kanyama C, Kouanfack C, Nyirenda S, Kivuyo SL, Boyer-Chammard T, Phiri S, Ngoma J, Shimwela M, Nkungu D, Fomete LN, Simbauranga R, Chawinga C, Ngakam N, Heller T, Lontsi SS, Aghakishiyeva E, Jalava K, Fuller S, Reid AM, Rajasingham R, Lawrence DS, Hosseinipour MC, Beaumont E, Bradley J, Jaffar S, Lortholary O, Harrison T, Molloy SF, Sturny-Leclere A, Loyse A; DREAMM Consortium. Reduction in mortality from HIV-related CNS infections in routine care in Africa (DREAMM): a before-and-after, implementation study. Lancet HIV. 2023 Oct;10(10):e663-e673. doi: 10.1016/S2352-3018(23)00182-0.
Other Identifiers
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16.0091
Identifier Type: -
Identifier Source: org_study_id
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