Evidence map›Paper›PMID 32333010›Full record

Trial reportTransactions of the Royal Society of Tropical Medicine and Hygiene2020

Feasibility of manual white blood cell counts as a predictor of neonatal sepsis in a low-resource setting.

Christian N Golding, Frederik Schaltz-Buchholzer, Lilica Sanca, Clara Clipet-Jensen, Christine S Benn, Nicholas Au, Kate Chipperfield, Tobias R Kollmann, Nelly A Amenyogbe

Open access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Transactions of the Royal Society of Tropical Medicine and Hygiene, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 35% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. The BCGMethodsX · 2025
    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

9 authors at 4 institutions in 3 countries.

Christian N GoldingBandim Health Project, Indepth Network, Apartado 861, Bissau 1004, Guinea-Bissau.
Frederik Schaltz-BuchholzerBandim Health Project, Indepth Network, Apartado 861, Bissau 1004, Guinea-Bissau.
Lilica SancaBandim Health Project, Indepth Network, Apartado 861, Bissau 1004, Guinea-Bissau.
Clara Clipet-JensenResearch Center for Vitamins and Vaccines, Statens Serum Institut, Artillerivej 5, Copenhagen S 2300, Denmark.
Christine S BennBandim Health Project, Indepth Network, Apartado 861, Bissau 1004, Guinea-Bissau.
Nicholas AuDepartment of Pathology and Laboratory Medicine, University of British Columbia, Rm. G227-2211 Wesbrook Mall, Vancouver, BC Canada V6T 2B5.
Kate ChipperfieldDepartment of Pathology and Laboratory Medicine, University of British Columbia, Rm. G227-2211 Wesbrook Mall, Vancouver, BC Canada V6T 2B5.
Tobias R KollmannDepartment of Pediatrics, University of British Columbia, Rm 2D19, 4480 Oak Street, Vancouver, BC Canada V6H 3V4.
Nelly A AmenyogbeDepartment of Experimental Medicine, University of British Columbia, 2775 Laurel Street, Vancouver, BC Canada V5Z 1M9.
University of British Columbia · CABandim Health Project · GWOdense University Hospital · DKStatens Serum Institut · DK

Funding

Transcriptomics to define biomarkers of neonatal vaccine immunogenicityU19AI118608 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI LEVY, OFER · 2017 to 2021
$24.7M
NIAID NIH HHS U19 AI118608
6 · The paper itself

Abstract

backgroundManual white blood cell (WBC) differential counts as a predictor for neonatal sepsis development in a low-resource setting have not been thoroughly evaluated. We hypothesized that manual differentiation (specifically immature:total [I:T] neutrophil ratios) would be feasible and useful as an adjunct to predict early-onset neonatal sepsis (EONS). Secondarily, we hypothesized that vaccination with bacillus Calmette-Guérin (BCG) and oral polio vaccine (OPV) could alter WBC differential counts and thus might reduce its predictive performance.

methodsWe performed a prospective cohort study within a randomized trial, randomizing healthy, high-risk newborns admitted to the nursery at the national hospital in Guinea-Bissau 1:1 to BCG+OPV at admission or at discharge (usual practice). Thin capillary blood films were prepared at 2 d of age in a subset of 268 neonates. WBC counts were assessed by microscopy and neonates were followed up for sepsis development within 2 weeks.

resultsNinety-eight percent (264/268) of smears provided interpretable reads. Of the 264 children, 136 had been randomized to receive BCG+OPV prior to sampling; the remaining 128 were vaccinated at discharge. The I:T ratio (average 0.017) was lower among children who did not develop clinical sepsis but did not predict sepsis (p=0.70). Only three children had an I:T ratio >0.2 (associated with a higher probability of clinical sepsis in previous studies) but did not develop sepsis. Immunization did not alter WBC composition.

conclusionsManual WBC differentials are feasible in low-resource settings. WBC differentials are not affected by standard newborn immunization. However, the I:T ratio had no value in predicting subsequent development of sepsis.

Indexed as

Neonatal SepsisSepsisChildFeasibility StudiesGuinea-BissauHumansInfant, NewbornLeukocyte CountProspective StudiesBCG Vaccineleukocyte countneonatal sepsisnewborn infantoral poliovirus vaccinewestern africa

Identifiers

PMID32333010
PMCPMC11491923
OpenAlexW3019507869

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.