Evidence map›Paper›PMID 38883219›Full record

ArticleClinical case reports2024

COVID-19-induced immune thrombocytopenia management approach: A case report and literature review.

Hatem Mahmoud Alahwal, Mansour Hani Alsharif, Mada Hani Alsharif, Abdullah Talal Almohammadi, Adel Fahad Al-Marzouki, Ahmed Saleh Barefah, Salem Mohammad Bahashwan, Osman Omer Radhwi, Ghazi Abdullah Damanhouri

Abstract readCase Reports
In one paragraph

Article in Clinical case reports, 2024. 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
–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

2 citing papers in PubMed.

  1. 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

9 authors.

Hatem Mahmoud AlahwalHematology Department, Faculty of Medicine King Abdulaziz University Jeddah Saudi Arabia.ORCID https://orcid.org/0000-0003-3961-0765
Mansour Hani AlsharifInternal Medicine Department, Al-Thagher General Hospital Jeddah Saudi Arabia.
Mada Hani AlsharifDepartment of Preventive Medicine - Directorate of Health Affairs Jeddah Saudi Arabia.
Abdullah Talal AlmohammadiHematology Department, Faculty of Medicine King Abdulaziz University Jeddah Saudi Arabia.ORCID https://orcid.org/0000-0002-1489-459X
Adel Fahad Al-MarzoukiHematology Department, Faculty of Medicine King Abdulaziz University Jeddah Saudi Arabia.ORCID https://orcid.org/0009-0003-7066-1939
Ahmed Saleh BarefahHematology Department, Faculty of Medicine King Abdulaziz University Jeddah Saudi Arabia.ORCID https://orcid.org/0000-0003-2009-3817
Salem Mohammad BahashwanHematology Department, Faculty of Medicine King Abdulaziz University Jeddah Saudi Arabia.ORCID https://orcid.org/0000-0002-5635-230X
Osman Omer RadhwiHematology Department, Faculty of Medicine King Abdulaziz University Jeddah Saudi Arabia.ORCID https://orcid.org/0000-0002-1578-3998
Ghazi Abdullah DamanhouriHematology Department, Faculty of Medicine King Abdulaziz University Jeddah Saudi Arabia.ORCID https://orcid.org/0000-0001-7127-2597

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Key Clinical Message: Vincristine therapy can be effective in refractory Immune thrombocytopenia (ITP) following COVID-19 vaccination. Our case report highlights the need for further research to establish standard management guidelines for COVID-19-vaccine-associated ITP. Abstract: Adult immune thrombocytopenia (ITP) can occur as a rare complication following several viral infections or a rare adverse event or complication of vaccination. In this paper, we report a case of a 39-year-old male patient with severe refractory ITP that began 4-weeks after receiving his third (booster) dose of the COVID-19 vaccine (BNT162b2, Pfizer-BioNTech). He was given oral dexamethasone 40 mg daily for 4 days followed by prednisone at 1 mg/kg (85 mg daily) for 10 days. In the following weeks, we attempted several other lines of therapy to treat his ITP, including anti-RhD immunoglobulin, which, unfortunately, caused moderate hemolysis requiring packed red blood cell transfusion, intravenous immunoglobulin (given at a subtherapeutic dose of 0.4 g/kg for only 1 day since it was not available), rituximab, and eltrombopag. The patient, unfortunately, showed no response to any of these treatments. This was an indicator to initiate salvage therapy with vincristine 2 mg weekly for 3 weeks. The patient's platelet count started to increase remarkably during the third week of vincristine and normalized after 4 weeks. We review the findings, clinical characteristics, and management approaches that were reported in the literature regarding COVID-19-vaccine-induced ITP. More in-depth research is needed to delineate standard guidelines for the management of such cases. This report underscores the importance of resorting to vincristine and eltrombopag as great options for severe and refractory ITP related to the COVID-19 vaccine.

Indexed as

COVID‐19refractorysevere immune thrombocytopenic purpuravaccination vincristine

Identifiers

PMID38883219
PMCPMC11176723

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Registered trials

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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.