Evidence map›Paper›PMID 16495259›Full record

Trial reportAntimicrobial agents and chemotherapy2006

Artesunate suppositories versus intramuscular artemether for treatment of severe malaria in children in Papua New Guinea.

Harin A Karunajeewa, John Reeder, Kerry Lorry, Elizah Dabod, Juliana Hamzah, Madhu Page-Sharp, Gregory M Chiswell, Kenneth F Ilett, Timothy M E Davis

Open access · greenAbstract readComparative StudyRandomized Controlled Trial
In one paragraph

Trial report in Antimicrobial agents and chemotherapy, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 5 pooled it
4.5field-weighted citation impact, top 6% 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

21 citing papers in PubMed, 5 syntheses or guidelines pooled it, 49 citations in OpenAlex.

  1. Artemether for severe malaria.The Cochrane database of systematic reviews · 2019
    Pooled it
  2. Artemether for severe malaria.The Cochrane database of systematic reviews · 2014
    Pooled it
  3. Pre-referral rectal artesunate for severe malaria.The Cochrane database of systematic reviews · 2014
    Pooled it
  4. Pooled it
  5. Malaria: severe, life-threatening.BMJ clinical evidence · 2011
    Pooled it
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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

9 authors at 3 institutions in 2 countries.

Harin A KarunajeewaMedicine Unit Fremantle, School of Medicine and Pharmacology, University of Western Australia, Crawley.
John Reeder
Kerry Lorry
Elizah Dabod
Juliana Hamzah
Madhu Page-Sharp
Gregory M Chiswell
Kenneth F Ilett
Timothy M E Davis
University of Western Australia · AUPapua New Guinea Institute of Medical Research · PGPathwest Laboratory Medicine · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Drug treatment of severe malaria must be rapidly effective. Suppositories may be valuable for childhood malaria when circumstances prevent oral or parenteral therapy. We compared artesunate suppositories (n = 41; 8 to 16 mg/kg of body weight at 0 and 12 h and then daily) with intramuscular (i.m.) artemether (n = 38; 3.2 mg/kg at 0 h and then 1.6 mg/kg daily) in an open-label, randomized trial with children with severe Plasmodium falciparum malaria in Papua New Guinea (PNG). Parasite density and temperature were measured every 6 h for > or = 72 h. Primary endpoints included times to 50% and 90% parasite clearance (PCT50 and PCT90) and the time to per os status. In a subset of 29 patients, plasma levels of artemether, artesunate, and their common active metabolite dihydroartemisinin were measured during the first 12 h. One suppository-treated patient with multiple complications died within 2 h of admission, but the remaining 78 recovered uneventfully. Compared to the artemether-treated children, those receiving artesunate suppositories had a significantly earlier mean PCT50 (9.1 versus 13.8 h; P = 0.008) and PCT90 (15.6 versus 20.4 h; P = 0.011). Mean time to per os status was similar for each group. Plasma concentrations of primary drug plus active metabolite were significantly higher in the artesunate suppository group at 2 h postdose. The earlier initial fall in parasitemia with artesunate is clinically advantageous and mirrors higher initial plasma concentrations of active drug/metabolite. In severely ill children with malaria in PNG, artesunate suppositories were at least as effective as i.m. artemether and may, therefore, be useful in settings where parenteral therapy cannot be given.

Indexed as

AntimalarialsArtemetherArtemisininsArtesunateBody WeightChildChild, PreschoolClinical Trials as TopicDeveloping CountriesEndemic DiseasesFemaleHumansInfantInjections, IntramuscularMalaria, FalciparumMaleAntimalarialsArtemetherArtemisininsArtesunateSesquiterpenesSuppositories

Identifiers

PMID16495259
PMCPMC1426445
OpenAlexW2162661614

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.