# Meningitis diagnosis, treatment, and outcomes in rural, northern Uganda: 2015–2024

**Authors:** Abigail Link, Mark Okwir, Betty Nabongo, Fred Okello, Jimmy Alal, David Meya, Paul R. Bohjanen

PMC · DOI: 10.1371/journal.pgph.0005800 · PLOS Global Public Health · 2026-01-12

## TL;DR

A study in northern Uganda shows that improved diagnostic tools for meningitis, especially in HIV-positive patients, increased diagnosis rates and improved outcomes.

## Contribution

The study introduces an expanded meningitis diagnosis and treatment program using molecular diagnostics, showing improved outcomes in a resource-limited setting.

## Key findings

- Confirmed meningitis etiologies increased from 13.7% to 42.2% with expanded diagnostic methods.
- Mortality improved in groups with enhanced diagnostic and treatment programs compared to historical controls.
- People living with HIV had higher mortality rates and more confirmed meningitis cases than those without HIV.

## Abstract

Meningitis affects over 2.5 million people worldwide, primarily within resource-limited regions of the meningitis belt of Africa. In 2017, we implemented a cryptococcal meningitis (CM) diagnosis and treatment program (CM-DTP) designed to improve CM outcomes. In 2021, a meningitis diagnosis and treatment program (MEN-DTP) began to include all etiologies of meningitis to assess the impact of expanded diagnosis and treatment of meningitis. We conducted a retrospective study utilizing clinical records from 1443 adult patients admitted to Lira Regional Referral Hospital (LRRH) over three time periods between 2015–2024. Group 1 included 321 patients in a historical control group; Group 2 consisted of 890 patients during the CM-DTP and Group 3 included 232 patients during the MEN-DTP. Group 1 received routine meningitis care, Group 2 received testing and treatment focused on CM, and Group 3 received expanded diagnostic testing, including gram stain, culture, PCR- and antigen-based testing. Meningitis diagnosis and in-hospital mortality outcomes were assessed to evaluate our programs. A confirmed meningitis etiology was found in 13.7% in Group 1, 20.7% in Group 2, and 42.2% in Group 3. In Group 3, confirmed etiologies were identified based on culture (n = 30), Pastorex LA (n = 23), BioFire PCR (n = 56), GeneXpert Ultra (n = 14), and serum or CSF CrAg LFA (n = 53). Overall, more confirmed etiologies of meningitis were identified among people living with HIV (PLWH) (n = 319) compared to those without HIV (n = 22) in Group 3. Antibiotic use increased with pre-admission antibiotic use doubling from Group 1 to Group 3 (10.6% to 27.2%). Compared to Group 1, mortality improved in Groups 2 and 3. Overall, PLWH had increased mortality compared to those without HIV (32.4% vs. 13.3%). Introduction of molecular diagnostics increased meningitis diagnoses and improved outcomes, particularly in those with CM. MEN-DTP increased confirmed diagnoses, yet half remained undiagnosed, supporting investigation of deep sequencing technologies.

## Linked entities

- **Diseases:** meningitis (MONDO:0021108), cryptococcal meningitis (MONDO:0005723)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** AGAP3 (ArfGAP with GTPase domain, ankyrin repeat and PH domain 3) [NCBI Gene 116988] {aka AGAP-3, CENTG3, CRAG, MRIP-1, cnt-g3}
- **Diseases:** coma (MESH:D003128), LRRH (MESH:D003428), Mortality (MESH:D003643), neck pain/stiffness (MESH:D019547), enterovirus (MESH:D004769), headache (MESH:D006261), viral meningoencephalitis (MESH:D014777), Meningitis (MESH:D008580), Pneumoniae (MESH:D011014), inflammation (MESH:D007249), acute meningitis syndrome (MESH:D000208), immunodeficiency (MESH:D007153), fever (MESH:D005334), fungal (MESH:D009181), irritability (MESH:D001523), bacterial (MESH:D001424), BM (MESH:D016920), infection (MESH:D007239), photophobia (MESH:D020795), CSF pleocytosis (MESH:D007964), HIV co-infection (MESH:D060085), MEM (MESH:D000093902), confusion (MESH:D003221), VM (MESH:D008587), varicella zoster (MESH:D020804), meningitis/encephalitis (MESH:D004660), cytomegalovirus (MESH:D003586), CM (MESH:D016919), tuberculosis (MESH:D014376), MEN (MESH:D018813), aseptic meningitis (MESH:D008582), Infectious Diseases (MESH:D003141), HIV and TB (MESH:D015658), seizure (MESH:D012640), TB (MESH:D014390)
- **Chemicals:** steroids (MESH:D013256), flucytosine (MESH:D005437), amphotericin B (MESH:D000666), fluconazole (MESH:D015725), India ink (MESH:C028433), amphotericin B deoxycholate (MESH:C059765), acyclovir (MESH:D000212), ceftriaxone (MESH:D002443), LAM (MESH:C050016), Ziehl (-)
- **Species:** Echovirus (species) [taxon 33758], Human alphaherpesvirus 1 (Herpes simplex virus type 1, no rank) [taxon 10298], Escherichia coli (E. coli, species) [taxon 562], Zika virus (no rank) [taxon 64320], West Nile virus (no rank) [taxon 11082], Human betaherpesvirus 6 (species) [taxon 10368], Mycobacterium tuberculosis (species) [taxon 1773], Homo sapiens (human, species) [taxon 9606], Human alphaherpesvirus 2 (no rank) [taxon 10310], Human immunodeficiency virus 1 (no rank) [taxon 11676], Human alphaherpesvirus 3 (Varicella-zoster virus, no rank) [taxon 10335], Cytomegalovirus (genus) [taxon 10358], Cryptococcus neoformans (Cryptococcus neoformans serotype A, species) [taxon 5207], Streptococcus pneumoniae (species) [taxon 1313], Neisseria (genus) [taxon 482], Klebsiella (genus) [taxon 570], human gammaherpesvirus 4 (Epstein Barr virus, no rank) [taxon 10376]

## Full text

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## Figures

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## References

55 references — full list in the complete paper: https://tomesphere.com/paper/PMC12795354/full.md

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Source: https://tomesphere.com/paper/PMC12795354