1. Safety of intravenous immunoglobulin in the elderly treated for a dysimmune neuromuscular disease.
- Author
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Lozeron P, Not A, Theaudin M, Denier C, Masnou P, Sarov M, Adam C, Cauquil C, and Adams D
- Subjects
- Adolescent, Adult, Age Factors, Aged, Aged, 80 and over, Cohort Studies, Comorbidity, Diabetes Mellitus epidemiology, Drug Eruptions etiology, Female, Guillain-Barre Syndrome drug therapy, Guillain-Barre Syndrome epidemiology, Heart Failure epidemiology, Humans, Hypertension epidemiology, Immunoglobulins, Intravenous therapeutic use, Immunologic Factors therapeutic use, Male, Middle Aged, Myasthenia Gravis drug therapy, Myasthenia Gravis epidemiology, Neuromuscular Diseases epidemiology, Overweight epidemiology, Paraproteinemias epidemiology, Peripheral Nervous System Diseases drug therapy, Peripheral Nervous System Diseases epidemiology, Polyradiculoneuropathy, Chronic Inflammatory Demyelinating drug therapy, Polyradiculoneuropathy, Chronic Inflammatory Demyelinating epidemiology, Renal Insufficiency, Chronic epidemiology, Retrospective Studies, Risk Factors, Venous Thrombosis epidemiology, Young Adult, Acute Kidney Injury chemically induced, Drug-Related Side Effects and Adverse Reactions epidemiology, Headache chemically induced, Hypertension chemically induced, Immunoglobulins, Intravenous adverse effects, Immunologic Factors adverse effects, Neuromuscular Diseases drug therapy
- Abstract
Introduction: Many patients treated with intravenous immunoglobulin (IVIg) are >60 years of age. Tolerability has yet to be demonstrated in this age group., Methods: This is a retrospective study of adverse reactions among consecutive patients treated with IVIg for neurological disorders. Risk factors were recorded. Correlation and relative risks were calculated for age, risk factors, IVIg course, daily dose, concentration, preparation, and duration of treatment. An infusion and monitoring protocol was applied., Results: Two hundred forty-four patients were reviewed, including 62% who were ≥60 years of age (total dose 1.8 ± 0.4 g/kg body weight, daily dose 30.3 ± 2.0 g). Sixty-nine percent received sugar-stabilized IVIg. Forty-nine percent presented with >1 risk factor. Adverse reactions occurred in 35% and led to treatment discontinuation in 5%, with a similar incidence among age groups. In patients ≥60 years old, sucrose-free IVIg administration was an independent predictor of adverse reactions, including renal failure., Conclusion: In the elderly, IVIg infusions are safe. Adverse reactions mainly depend on IVIg preparation and administration. Renal failure is not uncommon with sugar-free IVIg., (© 2016 Wiley Periodicals, Inc.)
- Published
- 2016
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