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适当的静脉注射免疫球蛋白(IVIG)剂量与继发性免疫缺陷的长期预后改善相关:一项前瞻性、非干预性研究。

Adequate IVIG dosing is associated with an improved long-term outcome in secondary immunodeficiency: A prospective, non-interventional study.

出版信息

Int J Clin Pharmacol Ther. 2024 Oct;62(10):448-459. doi: 10.5414/CP204595.

Abstract

OBJECTIVE

To assess the safety, tolerability, and effectiveness of the intravenous immunoglobulin (IVIG) Intratect 50 g/L in immunoglobulin replacement therapy (IgRT) in a prospective, large-scale non-interventional study (NIS). The analysis focused upon patients with secondary immunodeficiency (SID), the most frequent indication for IgRT in this NIS.

MATERIALS AND METHODS

Patients were enrolled at 123 centers in Germany. Each patient received IVIG as prescribed by the physician, guided by the Summary of Product Characteristics. Data were acquired from medical records and patients' questionnaires.

RESULTS

In the NIS, 3,563 patients were documented. The main indication for IgRT was SID (73.2%), followed by primary immunodeficiency (14.7%), immune thrombocytopenia (5.8%), and other indications (6.2%). Among the SID patients, 52.9% were male, mean age was 66.5 years, and most (63.8%) were IVIG-naïve. Their annual infection rate improved from 3.7 before documentation in the NIS to 1.1 during the first year of the study. IgG trough plasma levels increased during treatment (> 6 g/L: 44.5% of SID patients at study entry and 64.8% in long-term treatment) and were associated with a trend toward reduced infection rate (p = 0.08). A 1-year infection analysis showed a significantly lower infection risk in the medium- and high-dose groups than in the low-dose group (p = 0.028 and p = 0.017, respectively). Patients' treatment satisfaction and quality of life improved from baseline. Adverse drug reactions (ADRs) in SID occurred at a low frequency with 0.8% at infusion level. On the patient level, ADRs occurred in 251 (15.3%) SID patients, with chills (7.4%) and pyrexia (0.9%) reported most frequently.

CONCLUSION

Effectiveness, safety, and quality of life confirmed the positive benefit-risk profile of IgRT. Higher IVIG dosages per body weight led to higher IgG plasma trough levels, in turn leading to reduced infection rates. Obese patients may need body-weight-adjusted treatment to reduce the risk of infection.

摘要

目的

评估静脉注射免疫球蛋白(IVIG)Intratect 50g/L 在免疫球蛋白替代疗法(IgRT)中的安全性、耐受性和有效性,这是一项前瞻性、大规模的非干预性研究(NIS)。分析重点关注继发性免疫缺陷(SID)患者,这是该 NIS 中 IgRT 最常见的适应症。

材料和方法

在德国的 123 个中心招募了患者。每位患者根据医生的处方和产品特性摘要接受 IVIG 治疗。数据来自病历和患者问卷。

结果

在 NIS 中,共记录了 3563 名患者。IgRT 的主要适应症是 SID(73.2%),其次是原发性免疫缺陷(14.7%)、免疫性血小板减少症(5.8%)和其他适应症(6.2%)。在 SID 患者中,52.9%为男性,平均年龄为 66.5 岁,大多数(63.8%)为 IVIG 初治患者。他们的年感染率从 NIS 记录前的 3.7 次改善到研究第一年的 1.1 次。治疗期间 IgG 谷血浆水平升高(>6g/L:SID 患者在研究入组时为 44.5%,长期治疗时为 64.8%),感染率呈下降趋势(p=0.08)。1 年感染分析显示,中高剂量组的感染风险显著低于低剂量组(p=0.028 和 p=0.017)。患者的治疗满意度和生活质量从基线开始改善。SID 患者的药物不良反应(ADR)发生率较低,为 0.8%(输注水平)。在患者水平上,251 名(15.3%)SID 患者发生了 ADR,最常见的是寒战(7.4%)和发热(0.9%)。

结论

有效性、安全性和生活质量证实了 IgRT 的积极获益风险特征。较高的每公斤体重 IVIG 剂量导致更高的 IgG 血浆谷浓度,进而降低感染率。肥胖患者可能需要根据体重调整治疗以降低感染风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5d2/11425087/c2e8f6a5f08f/intjclinpharmacol-62-448-01.jpg

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