Evidence map›Paper›PMID 31796087›Full record

ArticleMalaria journal2019

En-route to the 'elimination' of genotypic chloroquine resistance in Western and Southern Zambia, 14 years after chloroquine withdrawal.

Lungowe Sitali, Mulenga C Mwenda, John M Miller, Daniel J Bridges, Moonga B Hawela, Elizabeth Chizema-Kawesha, James Chipeta, Bernt Lindtjørn

Open access · goldAbstract read
In one paragraph

Article in Malaria journal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 10% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. [Pcr-rflp genotyping ofMedecine tropicale et sante internationale · 2022
    Article
  3. Diagnosing the drug resistance signature inJournal of parasitic diseases : official organ of the Indian Society for Parasitology · 2021
    Review
  4. Article
  5. Article
  6. Article
  7. Malaria prophylaxis approach during COVID-19 pandemic.Travel medicine and infectious disease
    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

8 authors at 3 institutions in 2 countries.

Lungowe SitaliCentre for International Health, Faculty of Medicine, University of Bergen, Bergen, Norway. lungowesitali@gmail.com.ORCID http://orcid.org/0000-0002-8722-110X
Mulenga C MwendaPATH Malaria Control and Elimination Partnership in Africa (MACEPA), National Malaria Elimination Centre, Ministry of Health, Chainama Grounds, Lusaka, Zambia.
John M MillerPATH Malaria Control and Elimination Partnership in Africa (MACEPA), National Malaria Elimination Centre, Ministry of Health, Chainama Grounds, Lusaka, Zambia.
Daniel J BridgesPATH Malaria Control and Elimination Partnership in Africa (MACEPA), National Malaria Elimination Centre, Ministry of Health, Chainama Grounds, Lusaka, Zambia.
Moonga B HawelaMalaria Elimination Centre, Ministry of Health, Chainama Hospital and College Grounds, Lusaka, Zambia.
Elizabeth Chizema-KaweshaMalaria Elimination Centre, Ministry of Health, Chainama Hospital and College Grounds, Lusaka, Zambia.
James ChipetaSchool of Medicine and University Teaching Hospital Malaria Research Unit (SMUTH-MRU), Lusaka, Zambia.
Bernt LindtjørnCentre for International Health, Faculty of Medicine, University of Bergen, Bergen, Norway.
Ministry of Health · ZMUniversity Teaching Hospital · ZMUniversity of Bergen · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAnti-malarial resistance is, and continues to be a significant challenge in the fight against malaria and a threat to achieving malaria elimination. In Zambia, chloroquine (CQ), a safe, affordable and well-tolerated drug, was removed from use in 2003 due to high levels of resistance evidenced with treatment failure. This study sought to investigate the prevalence of chloroquine resistance markers in Southern and Western Provinces of Zambia 14 years after the withdrawal of CQ.

methodsData from a cross-sectional, all-age household survey, conducted during the peak malaria transmission season (April-May 2017) was analysed. During the all-age survey, socio-demographic information and coverage of malaria interventions were collected. Consenting individuals were tested for malaria with a rapid diagnostic test and a spot of blood collected on filter paper to create a dried blood spot (DBS). Photo-induced electronic transfer-polymerase chain reaction (PET-PCR) was used to analyse the DBS for the presence of all four malaria species. Plasmodium falciparum positive samples were analysed by high resolution melt (HRM) PCR to detect the presence of genotypic markers of drug resistance in the P. falciparum chloroquine resistance transporter (Pfcrt) and P. falciparum multi-drug resistance (Pfmdr) genes.

resultsA total of 181 P. falciparum positive samples were examined for pfcrt K76T and MDR N86. Of the 181 samples 155 successfully amplified for Pfcrt and 145 for Pfmdr N86. The overall prevalence of CQ drug-resistant parasites was 1.9% (3/155), with no significant difference between the two provinces. No N86Y/F mutations in the Pfmdr gene were observed in any of the sample.

conclusionThis study reveals the return of CQ sensitive parasites in Southern and Western Provinces of Zambia 14 years after its withdrawal. Surveillance of molecular resistant markers for anti-malarials should be included in the Malaria Elimination Programme so that resistance is monitored country wide.

Indexed as

GenotypeAntimalarialsATP-Binding Cassette TransportersChloroquineCross-Sectional StudiesDried Blood Spot TestingDrug ResistanceHumansMalaria, FalciparumMembrane Transport ProteinsPlasmodium falciparumPolymerase Chain ReactionPrevalenceProtozoan ProteinsTime FactorsZambiaAntimalarialsATP-Binding Cassette TransportersChloroquinemdr gene protein, PlasmodiumMembrane Transport ProteinsPfCRT protein, Plasmodium falciparumProtozoan ProteinsChloroquine resistanceChloroquine sensitivityGenotypesPlasmodium falciparumZambia

Identifiers

PMID31796087
PMCPMC6889585
OpenAlexW2992104721

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.