Evidence map›Paper›PMID 35719190›Full record

ArticleTrauma surgery & acute care open2022

Sickle cell trait and multisystem trauma: an unaddressed urgent knowledge gap.

Frazer A Tessema, Gabrielle Lapping-Carr, Murtala I Affini, Isaiah K Selkridge, Akosua Y Oppong, Tanisha A Jones, Tanya Zakrison

Open access · goldAbstract readEditorial
In one paragraph

Article in Trauma surgery & acute care open, 2022. 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
0.5field-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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Death due to sickle cell crisis: a case report.Forensic science, medicine, and pathology · 2024
    Article
  2. 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

7 authors at 2 institutions in 1 country.

Frazer A Tessema *University of Chicago Pritzker School of Medicine, Chicago, Illinois, USA.ORCID 0000-0001-9764-4205
Gabrielle Lapping-Carr *Department of Pediatric Hematology & Oncology, Biological Sciences Division, University of Chicago, Chicago, Illinois, USA.
Murtala I AffiniUniversity of Chicago Pritzker School of Medicine, Chicago, Illinois, USA.
Isaiah K SelkridgeUniversity of Chicago Pritzker School of Medicine, Chicago, Illinois, USA.
Akosua Y OppongUniversity of Chicago Pritzker School of Medicine, Chicago, Illinois, USA.
Tanisha A JonesDepartment of Pediatric Hematology & Oncology, Biological Sciences Division, University of Chicago, Chicago, Illinois, USA.
Tanya ZakrisonDepartment of Surgery, Biological Sciences Division, University of Chicago, Chicago, Illinois, USA.
University of Chicago · USBrigham and Women's Hospital · US

Funding

Summer Program to Increase Heart, Lung, and Blood Biomedical ResearchR25HL096383 · NHLBI · UNIVERSITY OF CHICAGO · PI CHRISTOPHER O OLOPADE, William F Parker · 2009 to 2026
$2.1M
NHLBI NIH HHS R25 HL096383
6 · The paper itself

Abstract

Sickle cell trait (SCT) has historically been considered a benign condition, but SCT-positive patients have increased baseline risk of venous thromboembolism and chronic kidney disease, as well as increased risk of sickled erythrocytes in settings of hypoxia, acidosis, and hypovolemia. Multisystem traumatic injuries are a common clinical scenario, in which hypoxia, acidosis, and hypovolemia occur; however, little is known about how SCT-positive status impacts outcomes in multisystem trauma. We conducted a scoping literature review to investigate what was known about SCT in the setting of multisystem trauma. In the 110+ years that sickle cell hemoglobinopathies have been known, only three studies have ever examined the relationship between SCT and multisystem traumas. All three articles were case reports. None of the articles intentionally measured the association between SCT and multisystem trauma outcomes; they only incidentally captured information on SCT. Our article then examines historical reasons why so little research has studied the pathophysiology of the multisystem trauma in patients with SCT. Among the reasons is that historical and logistical factors have long prevented patients from knowing their SCT-status: historical discriminations against SCT-positive patients in the 1960s and 1970s delayed federal mandating of SCT newborn screening until 2006, whereas difficulties communicating known SCT-status to afflicted children also contributed to lack of patient knowledge. In light of our findings, we offer specific calls to action for the trauma surgery research community: (1) consider testing for SCT in trauma patients that have unexpected complications, particularly venous thromboembolism, rhabdomyolysis, or renal failure and (2) support research to understand how SCT impacts multisystem trauma outcomes. We also offer specific guidelines about how to 'proceed with caution' in implementation of these goals in light of the troubled history of SCT testing and policy in the USA.

Indexed as

Health Care Quality, Access, And EvaluationMultiple Traumaquality improvementVenous thromboembolism

Identifiers

PMID35719190
PMCPMC9171217
OpenAlexW4281635503

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.