Nicolas Daniel Widjanarko, Anthony Ekaputra, Jessica Felicia Ang
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引用次数: 0
摘要
目的:帕米膦酸钠是纤维结构不良(FD)的主要治疗方法之一,有文献证明可改善患者的临床特征。然而,它的使用产生了不确定的结果。因此,本综述旨在探讨帕米膦酸盐对FD患者的几种临床和生化结果的影响。材料和方法:本综述按照系统评价和荟萃分析的首选报告项目(PRISMA)指南进行。使用MEDLINE、ProQuest、Wiley和EBSCO检索数据库检索文献。采用ROBINS-I (Risk of Bias In non - random Studies of Interventions)对纳入的研究进行质量评价,采用Review Manager (RevMan) 5.4进行meta分析。结果:分别有8项和7项研究用于meta分析和系统评价。结果显示,有两项研究具有低偏倚风险,六项研究具有中等偏倚风险。纳入meta分析的所有论文均显示,与治疗前相比,帕米膦酸钠治疗后骨痛减轻(p<0.00001)和血清碱性磷酸酶(SAP) (p=0.04)有显著差异。结论:本研究结果表明,帕米膦酸盐治疗可显著减轻FD患者骨痛,增加SAP。然而,应该进行更多年龄特异性样本和较低偏倚风险的试验,以确定总体结果的统计显著性。
A Systematic Review and Meta Analysis of Non-Randomized Interventional Studies on the Pamidronate Treatment Efficacy for Patients with Bone Fibrous Dysplasia
Objective: Pamidronate is one of the main therapies for Fibrous Dysplasia (FD), with documented enhancements in patients' clinical characteristics. Nevertheless, its usage has yielded inconclusive results. Therefore, this review aimed to investigate pamidronate’s impact on several clinical and biochemical outcomes in FD patients.
Materials and Methods: This review was conducted under the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. MEDLINE, ProQuest, Wiley, and EBSCO search databases were used to search the literature. Risk of Bias In Non-Randomized Studies of Interventions (ROBINS-I) was applied for quality assessment of the included studies and Review Manager (RevMan) 5.4 was employed in performing the meta-analysis.
Results: There are eight and seven studies used in the meta-analysis and systematic review, respectively. The results showed there are two studies with a low risk of bias and six with a moderate category. All papers included in this meta-analysis showed significant differences in the reduction of bone pain (p<0.00001) and serum alkaline phosphatase (SAP) (p=0.04) after pamidronate treatment compared to the before-treatment groups.
Conclusion: The findings of this study indicated that pamidronate therapy had been proven to significantly reduce bone pain and increase SAP in FD patients. However, trials with more age-specific samples and a lower risk of bias should be carried out to determine the statistical significance of overall results.