足够的 IVIG 剂量与继发性免疫缺陷的长期疗效改善有关:一项前瞻性、非干预性研究。

IF 0.9 4区 医学 Q4 PHARMACOLOGY & PHARMACY International journal of clinical pharmacology and therapeutics Pub Date : 2024-10-01 DOI:10.5414/CP204595
Artur Bauhofer, Ümniye Balaban, Sonja Schimo, Monika Mayer, Jörg Schüttrumpf, Stephan Borte
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引用次数: 0

摘要

目的在一项前瞻性大规模非干预研究(NIS)中,评估静脉注射免疫球蛋白(IVIG)Intratect 50 g/L 在免疫球蛋白替代疗法(IgRT)中的安全性、耐受性和有效性。分析的重点是继发性免疫缺陷(SID)患者,这也是该 NIS 中 IgRT 最常见的适应症:材料和方法:患者在德国的 123 个中心登记。每位患者都按照医生的处方并在产品特征概要的指导下接受了 IVIG 治疗。数据来自医疗记录和患者问卷调查:结果:NIS 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(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,大多数患者(63.8%)对 IVIG 一无所知。他们的年感染率从 NIS 记录前的 3.7 降至研究第一年的 1.1。在治疗过程中,IgG 谷丙转氨酶血浆水平升高(> 6 g/L:44.5% 的 SID 患者在研究开始时达到,64.8% 的患者在长期治疗中达到),并与感染率下降趋势相关(p = 0.08)。1年感染分析显示,中剂量组和高剂量组的感染风险明显低于低剂量组(分别为 p = 0.028 和 p = 0.017)。患者的治疗满意度和生活质量较基线有所提高。SID 的药物不良反应(ADR)发生率较低,输液水平为 0.8%。在患者层面,有251例(15.3%)SID患者出现了药物不良反应,其中以寒战(7.4%)和发热(0.9%)最为常见:结论:IgRT 的有效性、安全性和生活质量证实了其积极的效益-风险特征。按体重计算的IVIG剂量越高,IgG血浆谷值水平越高,从而降低了感染率。肥胖患者可能需要根据体重调整治疗剂量,以降低感染风险。
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Adequate IVIG dosing is associated with an improved long-term outcome in secondary immunodeficiency: A prospective, non-interventional study.

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.

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来源期刊
CiteScore
1.70
自引率
12.50%
发文量
116
审稿时长
4-8 weeks
期刊介绍: The International Journal of Clinical Pharmacology and Therapeutics appears monthly and publishes manuscripts containing original material with emphasis on the following topics: Clinical trials, Pharmacoepidemiology - Pharmacovigilance, Pharmacodynamics, Drug disposition and Pharmacokinetics, Quality assurance, Pharmacogenetics, Biotechnological drugs such as cytokines and recombinant antibiotics. Case reports on adverse reactions are also of interest.
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