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Quality of Life and Health-Care Resource Utilization Among Children with Primary Immunodeficiency Receiving Home Treatment with Subcutaneous Human Immunoglobulin

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Abstract

Introduction

Among patients with antibody deficiency, patient-reported outcomes are important for choosing between equally effective treatment regimens.

Patients and Methods

Twelve children (1.7–17.1 years) with primary immunodeficiency were switched from hospital-based intravenous IgG treatment to home treatment with subcutaneous IgG. Quality of life (Child Health Questionnaire) and health-care resource utilization were assessed at baseline and after 3 and 6 months.

Results

From the parents’ perspective, significant improvements were seen after 6 months for mental health (median difference; 95% confidence interval, 15.0; 0.0, 22.5); change in health (1.0; 0.0, 2.0); and family activities (12.5; 2.1, 25.0). From the children’s’ perspective, significant improvements were seen for role/social limitations-emotional at 3 (22.2; 11.1, 33.3) and 6 months (22.2; 11.1, 66.7) and global health at 6 months (35.0; 15.0, 55.0). There were no significant improvements in other concepts. Subcutaneous IgG treatment significantly reduced absence days, days spent on hospital/physician visits, and health-care-related expenses.

Conclusion

Switching to home-based subcutaneous IgG treatment led to significant improvements in quality of life and substantial cost savings.

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Acknowledgments

The authors would like to thank Dr Helen Wiggett of Dianthus Medical Limited for preparing the first draft of the manuscript. The study was funded by a research grant from Baxter Healthcare.

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Correspondence to Anders Fasth.

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Fasth, A., Nyström, J. Quality of Life and Health-Care Resource Utilization Among Children with Primary Immunodeficiency Receiving Home Treatment with Subcutaneous Human Immunoglobulin. J Clin Immunol 28, 370–378 (2008). https://doi.org/10.1007/s10875-008-9180-9

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  • DOI: https://doi.org/10.1007/s10875-008-9180-9

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