Evidence map›Paper›PMID 33175844›Full record

Observational studyPloS one2020

Increased malaria parasitaemia among adults living with HIV who have discontinued cotrimoxazole prophylaxis in Kitgum district, Uganda.

Philip Orishaba, Joan N Kalyango, Pauline Byakika-Kibwika, Emmanuel Arinaitwe, Bonnie Wandera, Thomas Katairo, Wani Muzeyi, Hildah Tendo Nansikombi, Alice Nakato, Tobius Mutabazi and 3 more

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 33% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 3 institutions in 2 countries.

Philip OrishabaClinical Epidemiology Unit, College of Health Sciences, Makerere University, Kampala, Uganda.ORCID 0000-0002-1236-8529
Joan N KalyangoClinical Epidemiology Unit, College of Health Sciences, Makerere University, Kampala, Uganda.
Pauline Byakika-KibwikaDepartment of Internal Medicine, College of Health Sciences, Makerere University, Kampala, Uganda.
Emmanuel ArinaitweInfectious Diseases Research Collaboration, Kampala, Uganda.
Bonnie WanderaInfectious Diseases Research Collaboration, Kampala, Uganda.
Thomas KatairoClinical Epidemiology Unit, College of Health Sciences, Makerere University, Kampala, Uganda.
Wani MuzeyiClinical Epidemiology Unit, College of Health Sciences, Makerere University, Kampala, Uganda.
Hildah Tendo NansikombiClinical Epidemiology Unit, College of Health Sciences, Makerere University, Kampala, Uganda.
Alice NakatoClinical Epidemiology Unit, College of Health Sciences, Makerere University, Kampala, Uganda.
Tobius MutabaziClinical Epidemiology Unit, College of Health Sciences, Makerere University, Kampala, Uganda.
Moses R KamyaDepartment of Internal Medicine, College of Health Sciences, Makerere University, Kampala, Uganda.
Grant DorseyDivision of Infectious Diseases, Department of Medicine, University of California San Francisco, San Francisco, California, United States of America.
Joaniter I NankabirwaClinical Epidemiology Unit, College of Health Sciences, Makerere University, Kampala, Uganda.
Makerere University · UGInfectious Diseases Research Collaboration · UGUniversity of California, San Francisco · US

Funding

Training In Malaria Research in UgandaD43TW007375 · FIC · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ROSENTHAL, PHILIP JON · 2005 to 2019
$2.9M
Training in malaria surveillance, epidemiology and implementation science research to strengthen malaria policy and control in UgandaD43TW010526 · FIC · MAKERERE UNIVERSITY COLLEGE OF HEALTH SCIENCES · PI MATTHEW G DORSEY, MOSES Robert KAMYA · 2017 to 2026
$2.3M
Impact of malaria control interventions on the infectious reservoir, host immunity, and drug resistance in UgandaK43TW010365 · FIC · INFECTIOUS DISEASES RES COLLABORATION · PI NANKABIRWA, JOANITER IMMACULATE · 2017 to 2021
$514k
FIC NIH HHS D43 TW007375FIC NIH HHS D43 TW010526FIC NIH HHS K43 TW010365
6 · The paper itself

Abstract

backgroundAlthough WHO recommends cotrimoxazole (CTX) discontinuation among HIV patients who have undergone immune recovery and are living in areas of low prevalence of malaria, some countries including Uganda recommend CTX discontinuation despite having a high malaria burden. We estimated the prevalence and factors associated with malaria parasitaemia among adults living with HIV attending hospital outpatient clinic before and after discontinuation of CTX prophylaxis.

methodsBetween March and April 2019, 599 participants aged 18 years and above, and attending Kitgum hospital HIV clinic in Uganda were enrolled in a cross study. A standardized questionnaire was administered and physical examination conducted. A finger-prick blood sample was collected for identification of malaria parasites by microscopy. The prevalence of parasitaemia was estimated and compared among participants on and those who had discontinued CTX prophylaxis, and factors associated with malaria parasitaemia assessed.

resultsOf the enrolled participants, 27 (4.5%) had malaria parasites and 452 (75.5%) had stopped CTX prophylaxis. Prevalence of malaria parasitaemia was significantly higher in participants who had stopped CTX prophylaxis (5.5% versus 1.4% p = 0.03) and increased with increasing duration since the discontinuation of prophylaxis. Compared to participants taking CTX, those who discontinued prophylaxis for 3-5 months and >5 months were more likely to have malaria parasites (adjusted prevalence ratio (aPR) = 1.64, 95% CI 0.37-7.29, p = 0.51, and aPR = 6.06, 95% CI 1.34-27.3, P = 0.02). Low CD4 count (< 250cells/mm3) was also associated with increased risk of having parasites (aPR = 4.31, 95% CI 2.13-8.73, p <0.001).

conclusionPeople from malaria endemic settings living with HIV have a higher prevalence of malaria parasitaemia following discontinuation of CTX compared to those still on prophylaxis. The risk increased with increasing duration since discontinuation of the prophylaxis. HIV patients should not discontinue CTX prophylaxis in areas of Uganda where the burden of malaria remains high. Other proven malaria control interventions may also be encouraged in HIV patients following discontinuation of CTX prophylaxis.

Indexed as

AdultAntimalarialsCross-Sectional StudiesFemaleHIV InfectionsHumansMalariaMaleMiddle AgedParasitemiaPlasmodiumPrevalenceTrimethoprim, Sulfamethoxazole Drug CombinationUgandaAntimalarialsTrimethoprim, Sulfamethoxazole Drug Combination

Identifiers

PMID33175844
PMCPMC7657524
OpenAlexW3101160401

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.