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皮下免疫球蛋白免疫疗法治疗自身免疫性神经肌肉疾病的疗效和患者满意度。

Efficacy and patient satisfaction in the use of subcutaneous immunoglobulin immunotherapy for the treatment of auto-immune neuromuscular diseases.

机构信息

Octapharma France, Boulogne, France.

Octapharma France, Boulogne, France.

出版信息

Autoimmun Rev. 2018 Sep;17(9):873-881. doi: 10.1016/j.autrev.2018.03.010. Epub 2018 Jul 10.

Abstract

We reviewed the efficacy of SCIg administration in terms of muscle strength maintenance and patient satisfaction comparing with IVIg in the treatment of auto-immune neuromuscular diseases. A systematic review was conducted, and identified studies from databases (PUBMED, EMBASE, EBSCO, Web of Science and Google Scholar) which were analyzed. The methodological quality of the selected publications was evaluated using the Newcastle-Ottawa Scale. Data were extracted from a total of 11 studies Fixed and random-effect model meta-analyses were performed. For the maintenance of muscle strength, Overall Neuropathy Limitations Scale (ONLS) data from 100 patients diagnosed with multifocal mononeuropathy (MMN) or chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) were pooled together. Switching to subcutaneous immunoglobulin administration led to a significant improvement (fixed effects model, p = 0.002). In data collected using the Medical Research Council Scale for Muscle Strength data from 140 patients with a wider range of disorders, a small but significant improvement in overall strength was observed in the SCIg group (p < 0.0001). In addition, the results of two studies measuring health-related quality of life and patient satisfaction were pooled. Data from 49 patients suffering from MMN, CIDP, and a variety of different myopathies demonstrated a small but significant increase in the mean 36-Item Short Form Survey (SF-36) scores (p < 0.0001). A highly significant difference was revealed when comparing data from 119 patients' responses to the Life Quality Index questionnaire (LQI) assessing patient satisfaction (p < 0.0001). This is the first analysis showing that SCIg is more effective than IVIg in improving Patient Reported Outcomes in auto-immune neuromuscular disease. These results should permit a broad range of patients to self-administer immunoglobulin treatments at home, potentially improving patient acceptability while reducing hospital visits and healthcare costs for the treatment of chronic auto-immune neuropathies.

摘要

我们回顾了 SCIg 给药在维持肌肉力量和患者满意度方面的疗效,与 IVIg 在治疗自身免疫性神经肌肉疾病方面进行了比较。进行了系统评价,并从数据库(PUBMED、EMBASE、EBSCO、Web of Science 和 Google Scholar)中确定了分析的研究。使用纽卡斯尔-渥太华量表评估所选出版物的方法学质量。从总共 11 项研究中提取数据,进行固定效应模型和随机效应模型荟萃分析。对于肌肉力量的维持,将 100 例多发性单神经病(MMN)或慢性炎症性脱髓鞘性多发性神经病(CIDP)患者的总体神经病变限制量表(ONLS)数据汇总在一起。转换为皮下免疫球蛋白给药可显著改善(固定效应模型,p=0.002)。在使用更广泛疾病范围的 140 例患者的肌肉力量医学研究委员会量表收集的数据中,SCIg 组的总体力量有较小但显著的改善(p<0.0001)。此外,还汇总了两项测量健康相关生活质量和患者满意度的研究结果。来自患有 MMN、CIDP 和各种不同肌病的 49 例患者的数据表明,36 项简短健康状况调查问卷(SF-36)评分的平均值略有增加(p<0.0001)。比较 119 例患者对生活质量指数问卷(LQI)评估患者满意度的反应数据时,发现存在高度显著差异(p<0.0001)。这是第一项分析表明,SCIg 在改善自身免疫性神经肌肉疾病患者报告的结果方面比 IVIg 更有效。这些结果应该允许广泛的患者在家中自行进行免疫球蛋白治疗,潜在地提高患者的可接受性,同时减少慢性自身免疫性神经病变治疗的就诊次数和医疗保健费用。

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