Evidence map›Paper›PMID 28493472›Full record

ReviewBritish journal of haematology2017

Turf wars: exploring splenomegaly in sickle cell disease in malaria-endemic regions.

Venée N Tubman, Julie Makani

Open access · bronzeAbstract readReview
In one paragraph

Review in British journal of haematology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

15 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Splenomegaly in Children and Adolescents.Frontiers in pediatrics · 2021
    Review
  10. Article
  11. Consequences ofFrontiers in endocrinology · 2020
    Article
  12. Article
  13. Review
  14. Article
  15. Prescription audit in a paediatric sickle cell clinic in South-West Nigeria: A cross-sectional retrospective study.Malawi medical journal : the journal of Medical Association of Malawi · 2017
    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

2 authors at 2 institutions in 2 countries.

Venée N TubmanTexas Children's Cancer and Hematology Centers, Houston, TX, USA.ORCID 0000-0002-5973-8507
Julie MakaniDepartment of Haematology and Blood Transfusion, Muhimbili University of Health and Allied Sciences, Dar-es-salaam, Tanzania.
Baylor College of Medicine · USMuhimbili University of Health and Allied Sciences · TZ

Funding

The Sickle Pan-African Research Consortium (SPARCO)U24HL135881 · NHLBI · MUHIMBILI UNIVERSITY/ ALLIED HLTH SCIS · PI MAKANI, JULIE · 2017 to 2025
$5.3M
Clinical Hematology Research Career Development Program (K12)K12HL087164 · NHLBI · BOSTON CHILDREN'S HOSPITAL · PI CANTOR, ALAN B. · 2006 to 2016
$3.9M
NHLBI NIH HHS K12 HL087164NHLBI NIH HHS U24 HL135881Wellcome Trust 093727
6 · The paper itself

Abstract

Sickle cell disease (SCD) is a group of recessively inherited disorders of erythrocyte function that presents an ongoing threat to reducing childhood and adult morbidity and mortality around the world. While decades of research have led to improved survival for SCD patients in wealthy countries, survival remains dismal in low- and middle-income countries. Much of the early mortality associated with SCD is attributed to increased risk of infections due to early loss of splenic function. In the West, bacterial infections with encapsulated organisms are a primary concern. In sub-Saharan Africa, where the majority of infants with SCD are born, the same is true. However malaria presents an additional threat to survival. The search for factors that define variability in sickle cell phenotypes should include environmental modifiers, such as malaria. Further exploration of this relationship could lead to novel strategies to reduce morbidity and mortality attributable to infections. In this review, we explore the interactions between SCD, malaria and the spleen to better understand how splenomegaly and splenic (dys)function may co-exist in patients with SCD living in malaria-endemic areas.

Indexed as

AfricaAnemia, Sickle CellEndemic DiseasesGlobal HealthHumansMalariaSpleenSplenomegalyimmune functionmalariamarginal zone B cellsickle cell diseasespleen

Identifiers

PMID28493472
PMCPMC5494998
OpenAlexW2613509107

What OpenQuestion holds

Textmetadata
LicenceTDM
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.