Adverse drug reactions of oral dexamethasone in children and adolescents with childhood acute lymphoblastic leukemia: a systematic review.

L. Hu, Ang Neo Kim Emily, Yeoh Eng Juh Allen
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Abstract

AIM To summarise and review the best available evidence on the poorer outcome of adverse drug reactions (ADRs) induced by oral dexamethasone in adolescents with Acute Lymphoblastic Leukaemia (ALL) than in children with ALL. METHODS Five databases for published literature were searched for the period 1990 to 2009. Additionally, the reference lists of all retrieved articles were further searched for additional references. Assessment for methodological quality was undertaken using a critical appraisal tool from JBI-SUMARI. Following the critical appraisal, data extraction was carried out using the data extraction tool from JBI-MAStaRI. Specific details about the study, design, data collection methods, participants, stage of therapy, type of adverse drug reaction, location of evidence and findings were then described and compiled into a table. Data synthesis was presented in a narrative format as the methodologically heterogeneous nature of the quantitative studies made it not appropriate to perform meta-analysis. RESULTS Eleven included studies, mostly descriptive, formed the basis of this systematic review. The ADRs induced by oral dexamethasone that have a poorer outlook in adolescents with ALL than in children with ALL are: transient hyperglycemia, infectious complications, thrombosis, thromboembolism and avascular necrosis. Adolescents were observed to have higher incidence and risk to these ADRs. In some included studies, adolescence age was found to be a predictor of the ADRs. CONCLUSION The results indicated that adolescents experience more severe ADRs induced by oral dexamethasone during ALL treatment than children. This phenomenon may be explained by the age-related variability in pharmacokinetics characteristics of dexamethasone between the adolescents and younger children as well as the impact of pubertal changes that occur in adolescents. The outcome of the ADRs however, may be inevitably affected by the presence of confounders such as co-administered drugs as well. IMPLICATION FOR PRACTICE The findings call for more attention to be given to ALL patients who are diagnosed at an adolescent age, especially when dexamethasone is administered. This will alert the healthcare professionals to watch for the ADRs when administering the treatment. Healthcare professionals should also inform caregivers and patients so that they can be more aware of the ADRs. IMPLICATION FOR RESEARCH Prospective studies involving a larger number of subjects should be carried out, with a focus on revising protocol's efficiency in monitoring dexamethasone-induced ADRs in ALL patients. Patient subgroups who are more vulnerable to such ADRs and often ignored in non-specific protocols should be identified and prophylactic interventions, such as early screening, proposed.
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口服地塞米松治疗儿童和青少年急性淋巴细胞白血病的不良反应:一项系统综述。
目的总结和回顾口服地塞米松在青少年急性淋巴细胞白血病(ALL)患者中引起的药物不良反应(adr)预后差于儿童急性淋巴细胞白血病(ALL)患者的最佳现有证据。方法检索1990 ~ 2009年5个数据库中已发表的文献。此外,进一步检索所有检索到的文章的参考文献列表以查找其他参考文献。使用JBI-SUMARI的关键评估工具进行方法学质量评估。在关键评估之后,使用JBI-MAStaRI的数据提取工具进行数据提取。然后描述研究的具体细节、设计、数据收集方法、参与者、治疗阶段、药物不良反应类型、证据的位置和结果,并将其汇编成表格。数据综合以叙述形式呈现,因为定量研究在方法上的异质性使其不适合进行荟萃分析。结果6项纳入的研究,大多是描述性的,构成了本系统评价的基础。口服地塞米松在ALL青少年患者中诱发的不良反应的前景比ALL儿童患者差,包括:短暂性高血糖、感染性并发症、血栓形成、血栓栓塞和缺血性坏死。观察到青少年发生这些不良反应的发生率和风险较高。在一些纳入的研究中,青少年年龄被发现是不良反应的一个预测因子。结论青少年在ALL治疗过程中口服地塞米松引起的不良反应较儿童严重。这种现象可以解释为地塞米松在青少年和幼儿之间药代动力学特征的年龄相关差异,以及青少年发生的青春期变化的影响。然而,不良反应的结果可能不可避免地受到混杂因素的影响,例如共同给药。对实践的启示研究结果呼吁更多地关注在青少年年龄诊断出的所有患者,特别是当使用地塞米松时。这将提醒医疗保健专业人员在进行治疗时注意不良反应。医疗保健专业人员还应告知护理人员和患者,以便他们能够更加了解不良反应。研究意义:应开展更多受试者的前瞻性研究,重点修订方案在监测ALL患者地塞米松引起的不良反应方面的效率。应确定易受此类不良反应影响且在非特异性方案中经常被忽视的患者亚组,并提出预防性干预措施,如早期筛查。
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