原发性和继发性免疫缺陷患者的免疫球蛋白替代治疗:输注方法对免疫球蛋白特异性生活质量感知和治疗满意度的影响

IF 2.6 4区 医学 Q2 ALLERGY
Rajiv Mallick, Noemi Hahn, Christopher Scalchunes
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引用次数: 0

摘要

背景:免疫球蛋白替代疗法(IgRT)是目前原发性抗体缺乏患者(大多数原发性免疫缺陷(PID)疾病)的标准治疗方法,越来越多的现实证据支持将其用于继发性免疫缺陷(SID)患者。输液方法和做法会影响患者对治疗的满意度和对健康相关生活质量的感知。方法:对美国PID和SID患者进行在线调查。本研究主要调查了两种IgRT输注方法,静脉免疫球蛋白治疗(IVIG)和皮下免疫球蛋白(SCIG)对患者报告预后(PRO)生活质量指数(LQI)工具的影响。还调查了患者报告的输液时间效率、身心健康状况(分别为PROMIS GPH-2和PROMIS GMH-2)、患者对症状状态(PASS)、上肢残疾(Quick DASH)和总体健康感知(通过GHP)的可接受性。结果:990例患者(IVIG 391例,SCIG 598例)的疗效分析。SCIG患者的中位总LQI评分(84.7)高于IVIG患者(81.9)(p结论:接受SCIG的患者的LQI评分显著高于接受IVIG的患者,证实了现有的证据,即SCIG替代IVIG可能会对适当选择的患者的免疫球蛋白特异性生活质量感知和治疗满意度产生有利影响。我们在输液时间方面的证据表明,在输液时间效率方面可能有类似的改进。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immunoglobulin replacement therapy in patients with primary and secondary immunodeficiencies: impact of infusion method on immunoglobulin-specific perceptions of quality of life and treatment satisfaction.

Background: Immunoglobulin replacement therapy (IgRT) is the current standard of care for primary antibody deficiency patients (majority of all primary immunodeficiency (PID) diseases), with growing real-world evidence supporting use for secondary immunodeficiency (SID) patients. Infusion methods and practices can affect patients' satisfaction with their treatment and perception of their health-related quality of life.

Methods: An online survey of US patients with PID and SID was conducted. This research investigates primarily the impact of two IgRT infusion methods, intravenous immunoglobulin therapy (IVIG) and subcutaneous immunoglobulin (SCIG), on the patient reported outcome (PRO) Life Quality Index (LQI) tool. Patient reported infusion time efficiency, physical and mental health (PROMIS GPH-2 and PROMIS GMH-2 respectively), patient acceptability of their symptom state (PASS), upper extremity disability (Quick DASH) and general health perception (via the GHP) are also investigated.

Results: Responses of 990 patients (391 IVIG and 598 SCIG) were analyzed. The median total LQI score amongst SCIG patients (84.7) was higher than IVIG patients (81.9) (p < 0.001), and was significantly higher on 3 out of 4 sub-domains of the LQI. SCIG patients scored higher on items that are related to convenience and reported less interference with everyday life: "Are convenient", "Are scheduled according to my convenience", "Do not interfere with my work/school" and "Require very little time and cost". However, there was no significant difference between the two patient cohorts on other, non-IG specific PROs (PASS, PROMIS GPH-2 and GMH-2 and Quick DASH). Patient reported time per infusion was lower for SCIG infusions than IVIG infusions (pre-infusion time; 22 min vs. 63 min, p < 0.001, infusion time; 120 min vs. 240 min, p < 0.001, post-infusion time; 9 min vs. 31 min, p < 0.001). IVIG patients also reported more interference with everyday life than SCIG patients (82 vs. 86, p < 0.001).

Conclusions: The significantly higher LQI scores for patients receiving SCIG than those receiving IVIG confirms existing evidence that substitution of SCIG for IVIG may favorably impact immunoglobulin specific perceptions of quality of life and treatment satisfaction for appropriately selected patients. Our evidence on infusion times indicates similar improvement may be possible on infusion time efficiency.

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来源期刊
CiteScore
4.30
自引率
3.70%
发文量
96
审稿时长
12 weeks
期刊介绍: Allergy, Asthma & Clinical Immunology (AACI), the official journal of the Canadian Society of Allergy and Clinical Immunology (CSACI), is an open access journal that encompasses all aspects of diagnosis, epidemiology, prevention and treatment of allergic and immunologic disease. By offering a high-visibility forum for new insights and discussions, AACI provides a platform for the dissemination of allergy and clinical immunology research and reviews amongst allergists, pulmonologists, immunologists and other physicians, healthcare workers, medical students and the public worldwide. AACI reports on basic research and clinically applied studies in the following areas and other related topics: asthma and occupational lung disease, rhinoconjunctivitis and rhinosinusitis, drug hypersensitivity, allergic skin diseases, urticaria and angioedema, venom hypersensitivity, anaphylaxis and food allergy, immunotherapy, immune modulators and biologics, immune deficiency and autoimmunity, T cell and B cell functions, regulatory T cells, natural killer cells, mast cell and eosinophil functions, complement abnormalities.
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