Evidence map›Paper›PMID 41922064›Full record

ArticleBMJ paediatrics open2026

Health-related quality of life in Chinese children with immune thrombocytopaenia: a multicentre study.

Shuxian Huang, Min Chen, Hui Zhang, Yongzhi Zheng, Sihan Huang, Zhiyuan Chen, Jinhong Luo, Liyun Xiao, Jinhua Chu, Biyun Guo and 5 more

Abstract readMulticenter Study
In one paragraph

Article in BMJ paediatrics open, 2026. 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

15 authors.

Shuxian Huang *Department of Pediatric Hematology, Rheumatology and Nephrology, Zhangzhou Affiliated Hospital of Fujian Medical University, Zhangzhou, China.ORCID http://orcid.org/0009-0006-6288-3736
Min Chen *Oncology Discipline Group, The Key Laboratory of Pediatric Hematology and Oncology Diseases of Wenzhou, Department of Hematology and Oncology, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Shanghai, China.ORCID http://orcid.org/0009-0009-1890-5282
Hui ZhangDepartment of Hematology, Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Yongzhi ZhengFujian Provincial Key Laboratory on Hematology, Fujian Institute of Hematology, Fuzhou, China.
Sihan HuangFujian Children's Hospital (Fujian Branch of Shanghai Children's Medical Center), College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Fuzhou, China.
Zhiyuan ChenDepartment of Pediatric Hematology, Rheumatology and Nephrology, Zhangzhou Affiliated Hospital of Fujian Medical University, Zhangzhou, China.
Jinhong LuoDepartment of Pediatric Hematology, Rheumatology and Nephrology, Zhangzhou Affiliated Hospital of Fujian Medical University, Zhangzhou, China.
Liyun XiaoDepartment of Pediatric Hematology, Rheumatology and Nephrology, Zhangzhou Affiliated Hospital of Fujian Medical University, Zhangzhou, China.ORCID http://orcid.org/0009-0000-7291-8732
Jinhua ChuDepartment of Hematology/Oncology, Pediatrics, Second Hospital of Anhui Medical University, Hefei, China.
Biyun GuoDepartment of Pediatrics, The First Affiliated Hospital of Xiamen University, Xiamen, China.ORCID http://orcid.org/0000-0002-5032-9213
Yan DaiPeople's Hospital of Guangxi Zhuang Autonomous Region, Nanning, Guangxi, China.
Yuantao HuangDepartment of Pediatrics, Longyan First Hospital of Fujian Medical University, Longyan, China.
Shuhong ShenDepartment of Hematology, Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Haixia Zhou *Oncology Discipline Group, The Key Laboratory of Pediatric Hematology and Oncology Diseases of Wenzhou, Department of Hematology and Oncology, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Shanghai, China.
Kaizhi Weng *Department of Pediatric Hematology, Rheumatology and Nephrology, Zhangzhou Affiliated Hospital of Fujian Medical University, Zhangzhou, China lqlrandywkz@163.com.ORCID http://orcid.org/0009-0006-4349-3150

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis multicentre, prospective study systematically evaluated health-related quality of life (HRQoL) in Chinese children with newly diagnosed immune thrombocytopaenia (ITP) using the disease-specific Kids' ITP Tools (KITs) scale. The study addresses a critical gap in longitudinal HRQoL data, particularly within South and East Asian paediatric populations.

methodsA total of 88 child self-reports, 215 parent proxy-reports and 303 parent-completed HRQoL assessments were collected from nine tertiary hospitals (2023 and 2025). HRQoL was measured using validated KITs scales (child self-report ≥7 years, parent proxy-report <7 years) at diagnosis and 1-week, 1-month, 3-month and 12-month follow-ups. Clinical variables were systematically recorded. Analyses included internal consistency (Cronbach's α), mixed-effects models and Spearman correlation testing.

resultsThe cohort comprised 88 self-reported children (mean age 9.2 years) and 215 parent proxy-reports (mean age 3.2 years). Major findings included: (1) significant parent-child discordance in HRQoL scores (mean difference 20.06 points at diagnosis, p<0.001), with parents consistently reporting poorer HRQoL; (2) excellent scale reliability (parent α=0.944, child α=0.910); (3) no association between baseline platelet counts and HRQoL (all p>0.05); (4) transient HRQoL reductions following bone marrow aspiration and glucocorticoid therapy and (5) age-specific patterns-older children reported greater family-related distress (p=0.044), whereas parents of younger children reported greater procedural distress (p<0.001).

conclusionThis study supports the cross-cultural validity and reliability of the KITs scale in paediatric ITP. It reveals marked parent-child discrepancies (20.06-point gap) likely influenced by cultural and psychosocial factors. These findings highlight the need for culturally informed family-centred psychosocial interventions and provide a foundation for international HRQoL comparisons and culturally adaptive clinical care models in paediatric haematology.

Indexed as

Purpura, Thrombocytopenic, IdiopathicQuality of LifeAdolescentChildChild, PreschoolChinaEast Asian PeopleFemaleHumansMaleParentsProspective StudiesSelf ReportSurveys and QuestionnairesChildChild HealthEthology

Identifiers

PMID41922064
PMCPMC13052635

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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.