Evidence map›Paper›PMID 39564062›Full record

ArticleCureus2024

Risk Stratification for Autoimmune Hemolytic Anemia in Children With Pediatric Transfusion-Dependent Thalassemia.

Arooj Khan, Faizan Sadiq, Shaista Azeem Khan, S Mohsin Ali Shah, Misbah Ullah Khan, Muhammad Khalid Khan, Anam Zaman, Abdur Rehman, Faran Sadiq, Muhammad Rahat Jan

Abstract read
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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.

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1 · What the graph read from it

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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

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3 · Its place in the literature

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No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Arooj KhanDepartment of Paediatrics, Khyber Medical College and Teaching Hospital, Peshawar, PAK.
Faizan SadiqDepartment of Paediatrics, Khyber Medical College and Teaching Hospital, Peshawar, PAK.
Shaista Azeem KhanDepartment of Paediatrics, Khyber Medical College and Teaching Hospital, Peshawar, PAK.
S Mohsin Ali ShahDepartment of Paediatrics, Khyber Medical College and Teaching Hospital, Peshawar, PAK.
Misbah Ullah KhanDepartment of Paediatrics, Khyber Medical College and Teaching Hospital, Peshawar, PAK.
Muhammad Khalid KhanDepartment of Paediatrics, Khyber Medical College and Teaching Hospital, Peshawar, PAK.
Anam ZamanDepartment of Paediatrics, Khyber Medical College and Teaching Hospital, Peshawar, PAK.
Abdur RehmanDepartment of Paediatrics, Khyber Medical College and Teaching Hospital, Peshawar, PAK.
Faran SadiqDepartment of Accident and Emergency, Lady Reading Hospital, Peshawar, PAK.
Muhammad Rahat JanDepartment of Accident and Emergency, Lady Reading Hospital, Peshawar, PAK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective This study aimed to identify the risk factors for autoimmune hemolytic anemia (AIHA) in children with transfusion-dependent thalassemia (TDT). Methodology This cross-sectional study was conducted at the Department of Child Health, Khyber Teaching Hospital, Peshawar, Pakistan, from March 25, 2024, to September 25, 2024. A total of 300 patients under 18 years of age, diagnosed with TDT, were included in the study. Relevant demographic, clinical, and laboratory investigations were conducted for each patient, with AIHA diagnosed based on the Coombs test. Risk factors, including demographic data, disease characteristics, transfusion history, clinical factors, and laboratory parameters, were recorded and analyzed. The significance of these risk factors was assessed by using the chi-square test for categorical variables and the independent t-test for continuous variables, comparing Coombs test-compatible and incompatible patients. A p-value of less than 0.05 was considered statistically significant. Results The mean±SD age of participants in this study was 6.82±4.2 years with an age range of one to 16 years. The male gender was 56.33%. The results of the Coombs test showed that 48.66% of these children had developed AIHA. The comparison between incompatible and compatible patients at Coombs test showed that age of patients (5.87±3.93 vs. 7.68±4.28 years, p = 0.00), age at the time of diagnosis (2.21±0.99 vs. 4.64±3.03 years, p = 0.00), age at the time of first infusion (3.05±1.28 vs. 5.49±3.2 years, p = 0.00), transfusion interval < 3 weeks (48.6% vs. 37%, p = 0.04) and duration of transfusion (2.87±3.2 vs. 2.21±1.93 years, p = 0.03) were the significant risk factors in the development of AIHA. Conclusion The patient's age, age at diagnosis, age at the time of first transfusion, the transfusion interval, and the duration of blood transfusion are the significant risk factors influencing the development of AIHA.

Indexed as

autoimmune hemolytic anemia (aiha)coombs testpediatric hematologyrisk factorstransfusion-dependent thalassemia (tdt)

Identifiers

PMID39564062
PMCPMC11574505

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