Evidence map›Paper›PMID 23916333›Full record

ReviewPathogens and global health2013

A current analysis of chemotherapy strategies for the treatment of human African trypanosomiasis.

Peter Babokhov, Adekunle O Sanyaolu, Wellington A Oyibo, Adetayo F Fagbenro-Beyioku, Nnaemeka C Iriemenam

Abstract readReview
In one paragraph

Review in Pathogens and global health, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 110 papers.

0numbers the graph read from it
0cells of the map it votes in
110citing papers in PubMed
6.9field-weighted citation impact, top 2% 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

110 citing papers in PubMed, 233 citations in OpenAlex.

  1. Trial
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  14. Ascofuranone antibiotic is a promising trypanocidal drug for nagana.The Onderstepoort journal of veterinary research · 2024
    Article
  15. Review
  16. Article
  17. Article
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  19. Molecular and phylogenetic analysis of a type K1 strainBiochemistry and biophysics reports · 2023
    Article
  20. Article

50 more citing papers are in PubMed but not listed here.

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

5 authors at 2 institutions in 2 countries.

Peter BabokhovUniversity of Massachusetts, Boston, MA, USA. pbabokhov@gmail.com
Adekunle O Sanyaolu
Wellington A Oyibo
Adetayo F Fagbenro-Beyioku
Nnaemeka C Iriemenam
University of Lagos · NGUniversity of Massachusetts Boston · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite the recent advances in drug research, finding a safe, effective, and easy to use chemotherapy for human African trypanosomiasis (HAT) remains a challenging task. The four current anti-trypanosomiasis drugs have major disadvantages that limit more widespread use of these drugs in the endemic regions of sub-Saharan Africa. Pentamidine and suramin are limited by their effectiveness against the only first stage of Trypanosoma brucei gambiense and Trypanosoma brucei rhodesiense, respectively. In addition, melarsoprol and eflornithine (two second stage drugs) each have disadvantages of their own. The former is toxic and has increasing treatment failures while the latter is expensive, laborious to administer, and lacks efficacy against T. b. rhodesiense. Furthermore, melarsoprol's toxicity and decreasing efficacy are glaring problems and phasing out the drug as a frontline treatment against T. b. gambiense is now possible with the emergence of competent, safe combination chemotherapies such as nifurtimox-eflornithine combination treatment (NECT). The future of eflornithine, on the other hand, is more promising. The drug is useful in the context of combination chemotherapy and potential orally administered analogues. Due to the limits of monotherapies, greater emphasis should be placed on the research and development of combination chemotherapies, based on the successful clinical tests with NECT and its current use as a frontline anti-trypanosomiasis treatment. This review discussed the current and future chemotherapy strategies for the treatment of HAT.

Indexed as

AfricaAntiprotozoal AgentsDrug ResistanceDrug TherapyDrug Therapy, CombinationHumansTrypanosoma brucei gambienseTrypanosoma brucei rhodesienseTrypanosomiasis, AfricanAntiprotozoal Agents

Identifiers

PMID23916333
PMCPMC4001453
OpenAlexW2077451644

What OpenQuestion holds

Textmetadata
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.