靶向疗法对药物诱发史蒂文斯-约翰逊综合征/毒性表皮坏死综合征患儿总住院时间影响的贝叶斯网络荟萃分析》(A Bayesian Network Meta-Analysis of the Effect of Targeted Therapies on the Total Length of Hospital Stay in Children with Drug-Induced Stevens-Johnson Syndrome/Toxic Epidermal Necrolysis Syndrome.
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A Bayesian NMA is used to compare and combine evidence from multiple studies and allows clinicians to estimate the relative effectiveness of different treatments/interventions while accounting for heterogeneity in the available evidence. <b><i>Methods:</i></b> We conducted a comprehensive electronic database search for studies compatible with our inclusion criteria. Six studies with 103 patients were included in the NMA; of them, 37 patients were treated with intravenous immunoglobulin (IVIG), 37 with systemic corticosteroids (CS), 23 with IVIG + CS, and 3 with Etanercept (ET) + CS. Patients with a median age of 10 years were included in the study. <b><i>Results:</i></b> CS had the highest probability of being the most optimal treatment for SJS/TEN in terms of shorter LOS based on the Surface Under the Cumulative Ranking curve levels, and CS + IVIG was associated with a statistically nonsignificant trend toward shorter LOS than IVIG alone. 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引用次数: 0
摘要
背景:史蒂文斯-约翰逊综合征(SJS)和中毒性表皮坏死(TEN)是一种罕见的可能危及生命的超敏性疾病,其特点是皮肤和粘膜广泛受累。然而,目前还没有标准化的循证治疗方法来减少 SJS/TEN 的并发症。本文旨在通过贝叶斯网络荟萃分析(NMA),从住院时间(LOS)的角度比较儿科SJS/TEN不同治疗方法的疗效。贝叶斯网络荟萃分析用于比较和合并来自多项研究的证据,使临床医生能够估计不同治疗/干预方法的相对有效性,同时考虑到现有证据的异质性。方法:我们对符合纳入标准的研究进行了全面的电子数据库搜索。6项研究共纳入103名患者;其中37名患者接受了静脉注射免疫球蛋白(IVIG)治疗,37名患者接受了全身皮质类固醇(CS)治疗,23名患者接受了IVIG+CS治疗,3名患者接受了Etanercept(ET)+CS治疗。患者的中位年龄为 10 岁。研究结果根据累积排名曲线下表面水平,CS最有可能成为缩短SJS/TEN生命周期的最佳治疗方法,CS+IVIG与单独使用IVIG相比,在统计学上有缩短生命周期的趋势。值得注意的是,就 LOS 而言,没有一种治疗方法比其他干预措施有明显的优势。结论目前的证据表明,与单独使用 IVIG 相比,联合使用 CS 和 IVIG 可能会缩短患者的生命周期。要就特定疗法对小儿 SJS/TEN LOS 的疗效得出明确结论,并制定更明确的治疗指南,还需要进行更大规模的随机对照试验。
A Bayesian Network Meta-Analysis of the Effect of Targeted Therapies on the Total Length of Hospital Stay in Children with Drug-Induced Stevens-Johnson Syndrome/Toxic Epidermal Necrolysis Syndrome.
Background: Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are rare potentially life-threatening hypersensitivity disorders characterized by widespread skin and mucosal involvement. However, there is no standardized evidence-based treatment to reduce the complications of SJS/TEN. This article aims to compare the efficacy of different treatments for pediatric SJS/TEN in terms of length of hospital stay (LOS) using a Bayesian network meta-analysis (NMA). A Bayesian NMA is used to compare and combine evidence from multiple studies and allows clinicians to estimate the relative effectiveness of different treatments/interventions while accounting for heterogeneity in the available evidence. Methods: We conducted a comprehensive electronic database search for studies compatible with our inclusion criteria. Six studies with 103 patients were included in the NMA; of them, 37 patients were treated with intravenous immunoglobulin (IVIG), 37 with systemic corticosteroids (CS), 23 with IVIG + CS, and 3 with Etanercept (ET) + CS. Patients with a median age of 10 years were included in the study. Results: CS had the highest probability of being the most optimal treatment for SJS/TEN in terms of shorter LOS based on the Surface Under the Cumulative Ranking curve levels, and CS + IVIG was associated with a statistically nonsignificant trend toward shorter LOS than IVIG alone. Remarkably, none of the treatments showed a significant benefit over the other interventions in terms of LOS. Conclusion: Current evidence suggests that coadministration of CS and IVIG may be associated with a shorter LOS than IVIG alone. Further research with larger randomized controlled trials is needed to reach a definitive conclusion about the efficacy of specific therapy on LOS in pediatric SJS/TEN and to establish more definitive treatment guidelines.
期刊介绍:
Pediatric Allergy, Immunology, and Pulmonology is a peer-reviewed journal designed to promote understanding and advance the treatment of respiratory, allergic, and immunologic diseases in children. The Journal delivers original translational, clinical, and epidemiologic research on the most common chronic illnesses of children—asthma and allergies—as well as many less common and rare diseases. It emphasizes the developmental implications of the morphological, physiological, pharmacological, and sociological components of these problems, as well as the impact of disease processes on families.
Pediatric Allergy, Immunology, and Pulmonology coverage includes:
-Functional and genetic immune deficiencies-
Interstitial lung diseases-
Both common and rare respiratory, allergic, and immunologic diseases-
Patient care-
Patient education research-
Public health policy-
International health studies