Evidence map›Paper›PMID 38406536›Full record

ArticleEJHaem2024

Transcranial Doppler ultrasound velocities in a population of unstudied African children with sickle cell anemia.

Nicole F O'Brien, Peter Moons, Hunter Johnson, Taty Tshimanga, Davin Ambitapio Musungufu, Robert Tandjeka Ekandji, Jean Pongo Mbaka, Lydia Kuseyila Babatila, Ludovic Mayindombe, Buba Giresse and 11 more

Open access · diamondAbstract read
In one paragraph

Article in EJHaem, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.7field-weighted citation impact, top 14% 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

6 citing papers in PubMed, 6 citations in OpenAlex.

  1. Trial
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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

21 authors at 8 institutions in 5 countries.

Nicole F O'BrienDepartment of Pediatrics Division of Critical Care Medicine Nationwide Children's Hospital, The Ohio State University Columbus Ohio USA.ORCID https://orcid.org/0000-0002-8826-8671
Peter MoonsDepartment of Pediatrics and Child Health Kamuzu University of Health Sciences Blantyre Malawi.
Hunter JohnsonDepartment of Pediatrics Division of Critical Care Medicine Nationwide Children's Hospital, The Ohio State University Columbus Ohio USA.
Taty TshimangaDepartement de Pediatrie Cliniques Universitaires de Kinshasa, Hopital Pediatrique de Kalembe Lembe, Universite De Kinshasa Kimwenza Lembe Republique Democratic du Congo.
Davin Ambitapio MusungufuCentre Medicale Evangelique Bunia, Ituri District Bunia Republique Democratic du Congo.
Robert Tandjeka EkandjiUniversite des Sciences et des Technologie de Lodja, L'Hopital General de Reference de Lodja, Sankuru District Lodja Republique Democratic du Congo.
Jean Pongo MbakaUniversite des Sciences et des Technologie de Lodja, L'Hopital General de Reference de Lodja, Sankuru District Lodja Republique Democratic du Congo.
Lydia Kuseyila BabatilaDepartement de Pediatrie Cliniques Universitaires de Kinshasa, Hopital Pediatrique de Kalembe Lembe, Universite De Kinshasa Kimwenza Lembe Republique Democratic du Congo.
Ludovic MayindombeDepartement de Pediatrie Cliniques Universitaires de Kinshasa, Hopital Pediatrique de Kalembe Lembe, Universite De Kinshasa Kimwenza Lembe Republique Democratic du Congo.
Buba GiresseDepartement de Pediatrie Cliniques Universitaires de Kinshasa, Hopital Pediatrique de Kalembe Lembe, Universite De Kinshasa Kimwenza Lembe Republique Democratic du Congo.
Suzanna MwanzaDepartment of Paediatrics Chipata Central Hospital Chipata Zambia.
Clement LupumpaulaChipata Central Hospital Chipata Zambia.
Janet Simanguwa ChilimaChipata Central Hospital Chipata Zambia.
Alice NanyangweUniversity Teaching Hospitals-Children's Hospital Lusaka Zambia.
Peter KabembaUniversity Teaching Hospitals-Children's Hospital Lusaka Zambia.
Lisa Nkole KafulaUniversity Teaching Hospitals-Children's Hospital Lusaka Zambia.
Tusekile PhiriQueen Elizabeth Central Hospital, The Blantyre Malaria Project, Chichiri Blantyre Malawi.
Sylvester JuneQueen Elizabeth Central Hospital, The Blantyre Malaria Project, Chichiri Blantyre Malawi.
Montfort Bernard GushuQueen Elizabeth Central Hospital, The Blantyre Malaria Project, Chichiri Blantyre Malawi.
George ChagalukaDepartment of Pediatrics and Child Health Kamuzu University of Health Sciences Blantyre Malawi.
Catherine M Chunda-LiyokaUniversity Teaching Hospitals-Children's Hospital Lusaka Zambia.
University of Kinshasa · CDUniversity Teaching Hospital · ZMQueen Elizabeth Central Hospital · MWLaboratoire National de Référence · MANationwide Children's Hospital · USUniversity of Malawi · MWSt Francis’ Hospital · ZMUniversité Evangélique en Afrique · CD

Funding

Transcranial Doppler Ultrasonography Clinical and Research Centers of Excellence in Sub-Saharan AfricaR21HD106252 · NICHD · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI OBRIEN, NICOLE · 2021 to 2022
$393k
NICHD NIH HHS R21 HD106252
6 · The paper itself

Abstract

The greatest burden of sickle cell anemia (SCA) globally occurs in sub-Saharan Africa, where significant morbidity and mortality occur secondary to SCA-induced vasculopathy and stroke. Transcranial Doppler ultrasound (TCD) can grade the severity of vasculopathy, with disease modifying therapy resulting in stroke reduction in high-risk children. However, TCD utilization for vasculopathy detection in African children with SCA remains understudied. The objective was to perform a prospective, observational study of TCD findings in a cohort of children with SCA from the Democratic Republic of the Congo, Zambia, and Malawi. A total of 770 children aged 2-17 years without prior stroke underwent screening TCD. A study was scored as low risk when the time-averaged maximum of the mean (TAMMX) in the middle cerebral artery or terminal internal carotid artery was <170 cm/s but >50 cm/s, conditional risk when 170-200 cm/s, and high risk when >200 cm/s. Low-risk studies were identified in 604 children (78%), conditional risk in 129 children (17%), and high risk in three children (0.4%). Additionally, 34 (4%) were scored as having an unknown risk study (TAMMX <50 cm/s). Over the course of 15 months of follow-up, 17 children (2.2%) developed new neurologic symptoms (six with low-risk studies, seven with conditional risk, and four with unknown risk). African children with SCA in this cohort had a low rate of high-risk TCD screening results, even in those who developed new neurologic symptoms. Stroke in this population may be multifactorial with vasculopathy representing only one determinant. The development of a sensitive stroke prediction bundle incorporating relevant elements may help to guide preventative therapies in high-risk children.

Indexed as

Africasickle cell anemiasickle cell diseasetranscranial Doppler ultrasound

Identifiers

PMID38406536
PMCPMC10887331
OpenAlexW4389144027

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.