Intravenous immunoglobulin in heart transplant recipients with mild to moderate hypogammaglobulinemia and infection
Background Hypogammaglobulinemia (HGG) is a complication of solid organ transplantation leading to increased risk of infections. Intravenous immunoglobulin G (IVIG) replacement in patients with HGG may be able to reduce risk and morbidity associated with infection; however, there is scarce data abou...
Saved in:
Published in | Clinical transplantation Vol. 36; no. 4; pp. e14571 - n/a |
---|---|
Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Denmark
01.04.2022
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | Background
Hypogammaglobulinemia (HGG) is a complication of solid organ transplantation leading to increased risk of infections. Intravenous immunoglobulin G (IVIG) replacement in patients with HGG may be able to reduce risk and morbidity associated with infection; however, there is scarce data about IVIG in mild to moderate HGG (IgG 400–700 mg/dl) and heart transplant recipients.
Methods
A single center, retrospective study was performed in heart transplant recipients with mild (IgG 500–700 mg/dl) to moderate (IgG 400–499 mg/dl) HGG in the presence of an infection.
Results
Forty‐two patients were included in this study; 19 patients (45.2%) received IVIG and 23 (54.8%) patients did not. Patients in the IVIG group received on average one dose of IVIG at 0.5 g/kg. No differences in incidence of new infection at 3 months (26.3% vs. 17.4%; P = .71) and 6 months (42.1% vs. 34.8%; P = .63) were observed between the IVIG and non‐IVIG groups. Infections based on mild or moderate HGG also had no differences at 3 and 6 months.
Conclusion
Our findings suggest that a single infusion of IVIG in mild to moderate HGG may have little to no benefit in reducing incidence of new infections. Larger prospective studies are needed to confirm these findings. |
---|---|
Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0902-0063 1399-0012 |
DOI: | 10.1111/ctr.14571 |