Evidence map›Paper›PMID 29519240›Full record

ArticleBMC medicine2018

Lactate clearance as a prognostic marker of mortality in severely ill febrile children in East Africa.

A Aramburo, Jim Todd, Elizabeth C George, Sarah Kiguli, Peter Olupot-Olupot, Robert O Opoka, Charles Engoru, Samuel O Akech, Richard Nyeko, George Mtove and 3 more

Open access · goldAbstract read
In one paragraph

Article in BMC medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 8% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 45 citations in OpenAlex.

  1. Pooled it
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  17. Continuous physiological monitoring using wearable technology to inform individual management of infectious diseases, public health and outbreak responses.International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2020
    Review
  18. Article
  19. Metabolic Acidosis in Critically Ill Cirrhotic Patients with Acute Kidney Injury.Journal of clinical and translational hepatology · 2019
    Article
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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

13 authors at 9 institutions in 4 countries.

A AramburoRoyal Brompton & Harefield NHS Foundation Trust, Sydney Street, London, SW3 6NP, UK.
Jim ToddLondon School of Hygiene and Tropical Medicine, 15-17, Tavistock Place WC1H 9SH, London, WC1H 9SH, UK.
Elizabeth C GeorgeMedical Research Council Clinical Trials Unit (MRC CTU) at UCL, 125 Aviation House, Kingsway, London, WC2B 6NH, UK.
Sarah KiguliDepartment of Paediatrics, Mulago Hospital, Makerere College of Health Sciences, PO Box 7072, Kampala, Uganda.
Peter Olupot-OlupotDepartment of Paediatrics, Mbale Regional Referral Hospital, Pallisa Road, PO Box 291, Mbale, Uganda.
Robert O OpokaDepartment of Paediatrics, Mulago Hospital, Makerere College of Health Sciences, PO Box 7072, Kampala, Uganda.
Charles EngoruDepartment of Paediatrics, Soroti Regional Referral Hospital, PO Box 289, Soroti, Uganda.
Samuel O AkechKilifi Clinical Trials Facility, KEMRI-Wellcome Trust Research Programme, PO Box 203, Nairobi, Kenya.
Richard NyekoSt Mary's Hospital, Lacor, PO Box 180, Gulu, Uganda.
George MtoveTeule Hospital, PO Box 81, Muheza, Tanzania.
Diana M GibbMedical Research Council Clinical Trials Unit (MRC CTU) at UCL, 125 Aviation House, Kingsway, London, WC2B 6NH, UK.
Abdel G BabikerMedical Research Council Clinical Trials Unit (MRC CTU) at UCL, 125 Aviation House, Kingsway, London, WC2B 6NH, UK.
Kathryn MaitlandKilifi Clinical Trials Facility, KEMRI-Wellcome Trust Research Programme, PO Box 203, Nairobi, Kenya. k.maitland@imperial.ac.uk.ORCID 0000-0002-0007-0645
MRC Clinical Trials Unit at UCL · GBKenya Medical Research Institute · KEMulago Hospital · UGLondon School of Hygiene & Tropical Medicine · GBMbale Hospital · UGRajabu St Augustine's, Hospitali Teule · TZRoyal Brompton & Harefield NHS Foundation Trust · GBSoroti Hospital · UGSt. Mary's Hospital Lacor · UG

Funding

Medical Research Council G0601027Medical Research Council G0801439
6 · The paper itself

Abstract

backgroundHyperlactataemia (HL) is a biomarker of disease severity that predicts mortality in patients with sepsis and malaria. Lactate clearance (LC) during resuscitation has been shown to be a prognostic factor of survival in critically ill adults, but little data exist for African children living in malaria-endemic areas.

methodsIn a secondary data analysis of severely ill febrile children included in the Fluid Expansion as Supportive Therapy (FEAST) resuscitation trial, we assessed the association between lactate levels at admission and LC at 8 h with all-cause mortality at 72 h (d72). LC was defined as a relative lactate decline ≥ 40% and/or lactate normalisation (lactate < 2.5 mmol/L).

resultsOf 3170 children in the FEAST trial, including 1719 children (57%) with Plasmodium falciparum malaria, 3008 (95%) had a baseline lactate measurement, 2127 (71%) had HL (lactate ≥ 2.5 mmol/L), and 1179 (39%) had severe HL (≥ 5 mmol/L). Within 72 h, 309 children (10.3%) died, of whom 284 (92%) had baseline HL. After adjustment for potential confounders, severe HL was strongly associated with mortality (Odds Ratio (OR) 6.96; 95% CI 3.52, 13.76, p < 0.001). This association was not modified by malaria status, despite children with malaria having a higher baseline lactate (median 4.6 mmol/L vs 3 mmol/L; p < 0.001) and a lower mortality rate (OR = 0.42; p < 0.001) compared to non-malarial cases. Sensitivity and specificity analysis identified a higher lactate on admission cut-off value predictive of d72 for children with malaria (5.2 mmol/L) than for those with other febrile illnesses (3.4 mmol/L). At 8 h, 2748/3008 survivors (91%) had a lactate measured, 1906 (63%) of whom had HL on admission, of whom 1014 (53%) fulfilled pre-defined LC criteria. After adjustment for confounders, LC independently predicted survival after 8 h (OR 0.24; 95% CI 0.14, 0.42; p < 0.001). Absence of LC (< 10%) at 8 h was strongly associated with death at 72 h (OR 4.62; 95% CI 2.7, 8.0; p < 0.001).

conclusionsIndependently of the underlying diagnosis, HL is a strong risk factor for death at 72 h in children admitted with severe febrile illnesses in Africa. Children able to clear lactate within 8 h had an improved chance of survival. These findings prompt the more widespread use of lactate and LC to identify children with severe disease and monitor response to treatment.

trial registrationISRCTN69856593 Registered 21 January 2009.

Indexed as

Africa, EasternChildChild, PreschoolCritical IllnessFemaleFeverHumansInfantLactic AcidMalariaMalePrognosisRisk FactorsSepsisLactic AcidChildrenClinical trialsEast AfricaHospital admissionHyperlactataemiaLactate clearanceMalariaMortalityRandomisedSepsis

Identifiers

PMID29519240
PMCPMC5844084
OpenAlexW2787154718

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

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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.