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Quality of Life Differences for Primary Immunodeficiency Patients on Home SCIG versus IVIG

BACKGROUND: Patients with primary immunodeficiency disease (PIDD) and antibody deficiency require lifelong immunoglobulin replacement therapy. While both subcutaneous immunoglobulin (SCIG) and intravenous immunoglobulin (IVIG) replacement therapy are effective in preventing infection, patients with...

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Autores principales: Anterasian, Christine, Duong, Richard, Gruenemeier, Peg, Ernst, Carol, Kitsen, Jessica, Geng, Bob
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6863943/
https://www.ncbi.nlm.nih.gov/pubmed/31673923
http://dx.doi.org/10.1007/s10875-019-00705-5
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author Anterasian, Christine
Duong, Richard
Gruenemeier, Peg
Ernst, Carol
Kitsen, Jessica
Geng, Bob
author_facet Anterasian, Christine
Duong, Richard
Gruenemeier, Peg
Ernst, Carol
Kitsen, Jessica
Geng, Bob
author_sort Anterasian, Christine
collection PubMed
description BACKGROUND: Patients with primary immunodeficiency disease (PIDD) and antibody deficiency require lifelong immunoglobulin replacement therapy. While both subcutaneous immunoglobulin (SCIG) and intravenous immunoglobulin (IVIG) replacement therapy are effective in preventing infection, patients with PIDD still experience worse health-related quality of life (hrQOL) outcomes. OBJECTIVE: Assess differences in hrQOL for PIDD patients receiving home SCIG versus IVIG. METHODS: SF-36 surveys were administered by a specialty pharmacy to 630 PIDD patients receiving home SCIG and IVIG at baseline and then every 3 months between 2014 and 2016. Results were analyzed using two-sample t tests and linear mixed effects model. Analysis was repeated for different age categories and trended over time. RESULTS: Patients receiving SCIG reported statistically significant higher energy fatigue scores (+ 9 points, p < 0.001) but lower perceived role limitations due to physical health scores (− 14 points, p < 0.001). These differences were only observed in patients > 36 years of age. There were no differences in the composite SF-36 score for patients receiving SCIG versus IVIG (+ 1, p = 0.66). Immunoglobulin-naïve patients all improved their hrQOL, but a larger improvement was seen in those initiating SCIG versus IVIG. CONCLUSION: Patients with PIDD on home IVIG versus SCIG have similar composite hrQOL scores as measured by the SF-36. In the adult population, initiating immunoglobulin replacement with SCIG may result in more hrQOL improvement compared with IVIG, although personal preferences should also be considered. CLINICAL IMPLICATIONS: Patients with PIDD on home IVIG versus SCIG have similar composite health-related quality of life scores as measured by the SF-36. CAPSULE SUMMARY: Patients with primary immune-deficiency on home IVIG versus SCIG have similar composite health-related quality of life scores as measured by the SF-36. Personal preferences are important in deciding whether to treat with IVIG or SCIG. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10875-019-00705-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-68639432019-12-05 Quality of Life Differences for Primary Immunodeficiency Patients on Home SCIG versus IVIG Anterasian, Christine Duong, Richard Gruenemeier, Peg Ernst, Carol Kitsen, Jessica Geng, Bob J Clin Immunol Original Article BACKGROUND: Patients with primary immunodeficiency disease (PIDD) and antibody deficiency require lifelong immunoglobulin replacement therapy. While both subcutaneous immunoglobulin (SCIG) and intravenous immunoglobulin (IVIG) replacement therapy are effective in preventing infection, patients with PIDD still experience worse health-related quality of life (hrQOL) outcomes. OBJECTIVE: Assess differences in hrQOL for PIDD patients receiving home SCIG versus IVIG. METHODS: SF-36 surveys were administered by a specialty pharmacy to 630 PIDD patients receiving home SCIG and IVIG at baseline and then every 3 months between 2014 and 2016. Results were analyzed using two-sample t tests and linear mixed effects model. Analysis was repeated for different age categories and trended over time. RESULTS: Patients receiving SCIG reported statistically significant higher energy fatigue scores (+ 9 points, p < 0.001) but lower perceived role limitations due to physical health scores (− 14 points, p < 0.001). These differences were only observed in patients > 36 years of age. There were no differences in the composite SF-36 score for patients receiving SCIG versus IVIG (+ 1, p = 0.66). Immunoglobulin-naïve patients all improved their hrQOL, but a larger improvement was seen in those initiating SCIG versus IVIG. CONCLUSION: Patients with PIDD on home IVIG versus SCIG have similar composite hrQOL scores as measured by the SF-36. In the adult population, initiating immunoglobulin replacement with SCIG may result in more hrQOL improvement compared with IVIG, although personal preferences should also be considered. CLINICAL IMPLICATIONS: Patients with PIDD on home IVIG versus SCIG have similar composite health-related quality of life scores as measured by the SF-36. CAPSULE SUMMARY: Patients with primary immune-deficiency on home IVIG versus SCIG have similar composite health-related quality of life scores as measured by the SF-36. Personal preferences are important in deciding whether to treat with IVIG or SCIG. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10875-019-00705-5) contains supplementary material, which is available to authorized users. Springer US 2019-11-01 2019 /pmc/articles/PMC6863943/ /pubmed/31673923 http://dx.doi.org/10.1007/s10875-019-00705-5 Text en © The Author(s) 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Anterasian, Christine
Duong, Richard
Gruenemeier, Peg
Ernst, Carol
Kitsen, Jessica
Geng, Bob
Quality of Life Differences for Primary Immunodeficiency Patients on Home SCIG versus IVIG
title Quality of Life Differences for Primary Immunodeficiency Patients on Home SCIG versus IVIG
title_full Quality of Life Differences for Primary Immunodeficiency Patients on Home SCIG versus IVIG
title_fullStr Quality of Life Differences for Primary Immunodeficiency Patients on Home SCIG versus IVIG
title_full_unstemmed Quality of Life Differences for Primary Immunodeficiency Patients on Home SCIG versus IVIG
title_short Quality of Life Differences for Primary Immunodeficiency Patients on Home SCIG versus IVIG
title_sort quality of life differences for primary immunodeficiency patients on home scig versus ivig
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6863943/
https://www.ncbi.nlm.nih.gov/pubmed/31673923
http://dx.doi.org/10.1007/s10875-019-00705-5
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