Evidence map›Paper›PMID 39867046›Full record

ArticleCureus2024

Sickle Cell Disease: A Potential Cause of Immune Thrombocytopenia.

Abdulwahab Ahmed A Alkhars, Mohammed A Alkadi, Hussain M Alwabari, Jagshak Mandong, Zahraa Y Almakinah

Abstract readCase Reports
In one paragraph

Article in Cureus, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Abdulwahab Ahmed A AlkharsInternal Medicine, King Fahad Hospital Hofuf, Hofuf, SAU.
Mohammed A AlkadiInternal Medicine, King Fahad Hospital Hofuf, Hofuf, SAU.
Hussain M AlwabariInternal Medicine, King Fahad Hospital Hofuf, Hofuf, SAU.
Jagshak MandongInternal Medicine, King Fahad Hospital Hofuf, Hofuf, SAU.
Zahraa Y AlmakinahInternal Medicine, King Fahad Hospital Hofuf, Hofuf, SAU.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sickle cell anemia (SCA) is one of the known hemoglobinopathies that result in red blood cell (RBC) destruction, among other complications. There are factors that make SCA an environment for autoimmune disease (AID). They include chronic inflammation, immune-mediated processes involved in SCA complications, and susceptibility to infections. Furthermore, immune thrombocytopenia (ITP) is a complex disorder characterized by immune imbalance that results in platelet destruction. We report a case of a 20-year-old patient with SCA presenting with a vaso-occlusive crisis (VOC) and unexplained thrombocytopenia. After ruling out secondary causes of the latter condition, the patient was challenged with steroid therapy. Interestingly, he showed a dramatic response in platelet count. This report emphasizes the potential role of SCA in the development of ITP and encourages further studies to explore the underlying immunological mechanisms.

Indexed as

adult sickle cell anemiaautoimmune diseaseimmune-mediated thrombocytopeniaimmune thrombocytopeniaitpplatelet disordersickle cell complicationssickle cell crisissickle cell disease (scd)thrombocytopenia

Identifiers

PMID39867046
PMCPMC11757937

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.