Evidence map›Paper›PMID 30006977›Full record

Trial reportInternational journal of laboratory hematology2018

Accurate light microscopic diagnosis of South-East Asian ovalocytosis.

Christian P Nixon, Ari W Satyagraha, Grayson L Baird, Alida R Harahap, Lydia V Panggalo, Lenny L Ekawati, Inge Sutanto, Din Syafruddin, J Kevin Baird

Abstract readComparative StudyMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in International journal of laboratory hematology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 36% 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

3 citing papers in PubMed, 9 citations in OpenAlex.

  1. Mapping Three Decades of Research on Southeast Asian Ovalocytosis: A Bibliometric Analysis.Mediterranean journal of hematology and infectious diseases · 2026
    Article
  2. Article
  3. 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 5 institutions in 4 countries.

Christian P NixonCenter for International Health Research, Rhode Island Hospital and Alpert Medical School of Brown University, Providence, Rhode Island.ORCID http://orcid.org/0000-0002-9243-5567
Ari W SatyagrahaEijkman Institute for Molecular Biology, Jakarta, Indonesia.
Grayson L BairdLifespan Biostatistics Core, Rhode Island Hospital, Providence, Rhode Island.
Alida R HarahapEijkman Institute for Molecular Biology, Jakarta, Indonesia.
Lydia V PanggaloEijkman Institute for Molecular Biology, Jakarta, Indonesia.
Lenny L EkawatiEijkman-Oxford Clinical Research Unit, Eijkman Institute for Molecular Biology, Jakarta, Indonesia.
Inge SutantoFaculty of Medicine, University of Indonesia, Jakarta, Indonesia.
Din SyafruddinEijkman Institute for Molecular Biology, Jakarta, Indonesia.
J Kevin BairdEijkman-Oxford Clinical Research Unit, Eijkman Institute for Molecular Biology, Jakarta, Indonesia.
Eijkman Institute for Molecular Biology · IDAngkor Hospital for Children · KHBrown University · USProvidence College · USUniversity of Indonesia · ID

Funding

Statistics and Data Management P20GM104317 · NIGMS · UNIVERSITY OF RHODE ISLAND · PI MICHELOW, IAN · 2013 to 2017
$9.8M
National Institute of General Medical Sciences #1P20GM104317-01NIGMS NIH HHS P20 GM104317
6 · The paper itself

Abstract

introductionSouth-East Asian ovalocytosis (SAO) is a common inherited red blood cell polymorphism in South-East Asian and Melanesian populations, coinciding with areas of malaria endemicity. Validation of light microscopy as a diagnostic alternative to molecular genotyping may allow for its cost-effective use either prospectively or retrospectively by analysis of archived blood smears.

methodsWe assessed light microscopic diagnosis of SAO compared to standard PCR genotyping. Three trained microscopists each assessed the same 971 Giemsa-stained thin blood films for which SAO genotypic confirmation was available by PCR. Generalized mixed modeling was used to estimate the sensitivity, specificity, positive predictive value, and negative predictive value of light microscopy vs "gold standard" PCR.

resultsAmong red cell morphologic parameters evaluated, knizocytes, rather than ovalocytic morphology, proved the strongest predictor of SAO status (odds ratio [OR] = 19.2; 95% confidence interval [95% CI] = 14.6-25.3; P ≤ 0.0001). The diagnostic performance of a knizocyte-centric microscopic approach was microscopist dependent: two microscopists applied this approach with a sensitivity of 0.89 and a specificity of 0.93. Inter-rater reliability among the microscopists (κ = 0.20) as well as between gold standard and microscopist (κ = 0.36) underperformed due to misclassification of stomatocytes as knizocytes by one microscopist, but improved substantially when excluding the error-prone reader (κ = 0.65 and 0.74, respectively).

conclusionLight microscopic diagnosis of SAO by knizocyte visual cue performed comparable to time-consuming and costlier molecular methods, but requires specific training that includes successful differentiation of knizocytes from stomatocytes.

Indexed as

Elliptocytosis, HereditaryErythrocytes, AbnormalAsia, SoutheasternFemaleHumansMicroscopyPolymerase Chain Reactioninter-rater diagnostic performanceknizocyteslight microscopymalariaSouth-East Asian ovalocytosis

Identifiers

PMID30006977
PMCPMC6246802
OpenAlexW2884660722

What OpenQuestion holds

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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.