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Driving Reduced AIDS-associated Meningo-encephalitis Mortality

Integrating the Diagnosis and Management of HIV-associated Central Nervous System (CNS) Infections Into Routine Health Services in Low and Middle Income Countries (LMICs)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03226379
Acronym
DREAMM
Enrollment
495
Registered
2017-07-21
Start date
2016-04-23
Completion date
2021-09-30
Last updated
2022-05-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

AIDS-Related Opportunistic Infections, Bacterial Meningitis, Cerebral Toxoplasmosis, Cryptococcal Meningitis, Meningo-encephalitis, Tuberculous Meningitis

Keywords

HIV related Meningitis, AIDS-Related Opportunistic Infections, Advanced HIV Disease, Health Systems Strengthening, Education Programmes

Brief summary

The DREAMM project is investigating whether the DREAMM interventions (1) Health system strengthening, 2) Co-designed education programs tailored to frontline healthcare workers, 3) Implementation of a diagnostic and treatment algorithm and, 4) Communities of practice in infectious diseases and laboratory capacity building) when combined reduce two week all-cause mortality of HIV-associated meningo-encephalitis in African LMICs.

Detailed description

HIV-associated central nervous system (CNS) infection causes significant mortality and places a high burden on limited health care resources in Sub-Saharan Africa (SSA). Cohort and autopsy studies estimate that CNS infections cause up to a third of HIV-related deaths in African LMICs. 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.

Interventions

OTHERDREAMM

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

Sponsors

European and Developing Countries Clinical Trials Partnership (EDCTP)
CollaboratorOTHER_GOV
National Agency for Research on AIDS and Viral Hepatitis (ANRS)
CollaboratorOTHER
Institut Pasteur
CollaboratorINDUSTRY
National Institute for Medical Research, Tanzania
CollaboratorOTHER_GOV
Amana Hospital, Dar es Salaam, Tanzania
CollaboratorUNKNOWN
University of North Carolina Project-Malawi (UNC Project), Lilongwe, Malawi
CollaboratorUNKNOWN
Kamuzu Central Hospital
CollaboratorOTHER
Yaounde Central Hospital
CollaboratorOTHER_GOV
Zomba Central Hospital, Zomba, Malawi
CollaboratorUNKNOWN
Lighthouse Trust
CollaboratorOTHER
Mwananyamala Hospital, Dar es Salaam, Tanzania
CollaboratorUNKNOWN
St George's, University of London
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SEQUENTIAL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Intervention model description

Cohort study with a before and after design

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Consecutive patients \> 18 years with 1st episode of suspected meningo- encephalitis 2. Known to be HIV positive or willing to undertake an HIV test 3. Willing to agree to participate in the study

Exclusion criteria

1. Patients presenting with suspected relapse of HIV-associated meningo-encephalitis 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.

Design outcomes

Primary

MeasureTime frameDescription
2-week all-cause mortality2 weeks from enrolment2-week all-cause mortality from enrolment

Secondary

MeasureTime frameDescription
4-week all-cause mortality4 weeks from enrolment4-week all-cause mortality 4 weeks from enrolment
10-week and 6-month rate of death10 weeks and 6 months from enrolment10-week and 6-month rate of death 10 weeks and 6 months from enrolment
Time to appropriate investigation: lumbar puncture, brain imaging10 weeks from enrolmentTime to appropriate investigation: lumbar puncture, brain imaging 10 weeks from enrolment
10-week all-cause mortality10 weeks from enrolment10-week all-cause mortality from enrolment
Prevalence of cryptococcal, tuberculous and bacterial meningitis and toxoplasma meningo-encephalitis and neurosyphilis10 weeks from enrolmentPrevalence of cryptococcal, tuberculous and bacterial meningitis and toxoplasma 10 weeks from enrolment
Time to ART initiation10 weeks from enrolmentTime to ART initiation 10 weeks from enrolment
6-month all-cause mortality6 months from enrolment6-month all-cause mortality 6 months from enrolment
Time to appropriate, microbiologically guided treatment10 weeks from enrolmentTime to appropriate, microbiologically guided treatment 10 weeks from enrolment

Countries

Cameroon, Malawi, Tanzania

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 10, 2026