Evidence map›Paper›PMID 36310636›Full record

ArticleGlobal pediatric health2022

Red Blood Cell Alloimmunization in Pediatric group with Beta Thalassemia: A Five-Year Experience.

Kiran Minhas, Muzamil Shabana Ejaz, Alaa Tukruna, Maryam Haider, Aabiya Arif, Sameer Saleem Tebha

Abstract read
In one paragraph

Article in Global pediatric health, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Observational
  2. Article
  3. 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

6 authors.

Kiran MinhasDow Medical College, Karachi, Pakistan.
Muzamil Shabana EjazDow Medical College, Karachi, Pakistan.
Alaa TukrunaBatterjee Medical College, Jeddah, KSA.
Maryam HaiderJinnah Medical and Dental College, Karachi, Pakistan.
Aabiya ArifZiauddin Medical College, Karachi, Pakistan.
Sameer Saleem TebhaJinnah Medical and Dental College, Karachi, Pakistan.ORCID https://orcid.org/0000-0001-8480-6148

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Beta-thalassemia is one of the most frequently occurring hematological disorders in [Removed for blinded peer-review]. Regular blood transfusion is required in almost all cases for management. However, this is associated with significant major complications like red blood cell (RBC) alloimmunization. This retrospective cross-sectional is conducted to evaluate the RBC alloimmunization frequency in children with beta-thalassemia aged between 6 months and 16 years in [Removed for blinded peer-review]. Antibody screening was performed using the Dia clon3 cell antigen panel. If the screening came back positive, a detailed panel was created for the identification of specific antibody. In our sample, the frequency of RBC alloimmunization was found in 22 (26.19%) patients. Of these 22 patients, the Rhesus system was found in most patients 17 (77.3%), followed by Kell 5 (22.7%). RBC alloimmunization was significantly associated with a family history of a blood disorder and splenectomy.

Indexed as

antibodybeta-thalassemiablood transfusionred blood cell alloimmunization

Identifiers

PMID36310636
PMCPMC9608007

What OpenQuestion holds

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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.