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急性淋巴细胞白血病患者的骨坏死:一项全国性问卷调查研究。

Osteonecrosis in patients with acute lymphoblastic leukaemia: a national questionnaire study.

作者信息

Amin Nadia Laila, Feltbower Richard, Kinsey Sally, Vora Ajay, James Beki

机构信息

Paediatric haematology, Leeds Children's Hospital, Leeds, UK.

University of Leeds, Leeds, UK.

出版信息

BMJ Paediatr Open. 2017 Sep 11;1(1):e000122. doi: 10.1136/bmjpo-2017-000122. eCollection 2017.

Abstract

OBJECTIVES

To establish prevalence, management and long-term outcomes of osteonecrosis (ON) in young people diagnosed with acute lymphoblastic leukaemia (ALL) between 2003 and 2011.

DESIGN SETTING PARTICIPANTS

This study assessed ON in 3113 patients aged 1-24 years who participated in the UK national leukaemia study UKALL 2003. UKALL 2003 recruited patients in 40 UK hospitals between 2003 and 2011 and included patients between ages 1 and 25 diagnosed with ALL.

RESULTS

170 patients were diagnosed with ON, giving a prevalence of 5.5%. The multivariable analysis showed that the risk of ON was highest for children aged between 10 and 20 years (ages 10-15 years, OR 23.7, 95% CI 14.8 to 38.0; ages 16-20 years, OR 22.5, 95% CI 12.7 to 39.8, compared with age <10 years). Among ethnic groups, Asian patients had the highest risk of ON (OR 1.92, 95% CI 1.1 to 3.6, compared with White patients). Eighty-five per cent of patients with ON had multifocal ON. Thirty-eight per cent of patients with ON required surgery and 19% of patients with ON required a hip replacement. Fifteen per cent of patients who had surgery still describe significant disability or use of a wheelchair.

CONCLUSIONS

ON has considerable morbidity for patients being treated for ALL, with a high burden of surgery. Age and ethnicity were found to be the most significant risk factors for development of ON, with Asian patients and patients aged 10-20 years at diagnosis of ALL at greatest risk. These results will help risk stratify patients at diagnosis of ALL, and help tailor future prospective studies in this area.

摘要

目的

确定2003年至2011年间诊断为急性淋巴细胞白血病(ALL)的年轻人中骨坏死(ON)的患病率、治疗情况及长期预后。

设计、地点、参与者:本研究评估了参与英国全国白血病研究UKALL 2003的3113名1至24岁患者的骨坏死情况。UKALL 2003于2003年至2011年在英国40家医院招募患者,纳入了年龄在1至25岁之间诊断为ALL的患者。

结果

170名患者被诊断为骨坏死,患病率为5.5%。多变量分析显示,10至20岁儿童发生骨坏死的风险最高(10至15岁,比值比23.7,95%置信区间14.8至38.0;16至20岁,比值比22.5,95%置信区间12.7至39.8,与年龄<10岁相比)。在不同种族中,亚洲患者发生骨坏死的风险最高(与白人患者相比,比值比1.92,95%置信区间1.1至3.6)。85%的骨坏死患者为多灶性骨坏死。38%的骨坏死患者需要手术,19%的骨坏死患者需要进行髋关节置换。接受手术的患者中有15%仍表示有明显残疾或需要使用轮椅。

结论

对于接受ALL治疗的患者,骨坏死具有相当高的发病率,手术负担沉重。年龄和种族被发现是发生骨坏死的最重要风险因素,亚洲患者以及诊断为ALL时年龄在

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/982f/5862222/417151fd1b51/bmjpo-2017-000122f01.jpg

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