Abstract | BACKGROUND: OBJECTIVE: METHODS: This is a retrospective chart review. RESULTS: LIMITATIONS: This is a retrospective review with only 2 cases. CONCLUSIONS: We propose that IVIG-associated hemolysis is an adverse reaction that may not be as rare as once thought, presenting as a mild decrease in hemoglobin and hematocrit. Antibodies to blood type A and B are given as part of pooled immune globulin and are considered to be the cause of hemolysis. More severe anemia requiring transfusion is less common, and the breakdown products produced by hemolysis can lead to pigment nephropathy and renal failure. We present methods by which this severe complication can be anticipated and managed more effectively.
|
Authors | Marnie R Ririe, Robert C Blaylock, Stephen E Morris, Jae Y Jung |
Journal | Journal of the American Academy of Dermatology
(J Am Acad Dermatol)
Vol. 69
Issue 2
Pg. 221-5
(Aug 2013)
ISSN: 1097-6787 [Electronic] United States |
PMID | 23673282
(Publication Type: Case Reports, Journal Article)
|
Copyright | Copyright © 2013 American Academy of Dermatology, Inc. Published by Mosby, Inc. All rights reserved. |
Chemical References |
- Immunoglobulins, Intravenous
|
Topics |
- Acute Kidney Injury
(chemically induced, therapy)
- Blood Transfusion
- Disease Progression
- Dose-Response Relationship, Drug
- Drug Administration Schedule
- Follow-Up Studies
- Hemolysis
(drug effects)
- Humans
- Immunoglobulins, Intravenous
(adverse effects, therapeutic use)
- Male
- Middle Aged
- Renal Dialysis
- Retrospective Studies
- Risk Assessment
- Severity of Illness Index
- Stevens-Johnson Syndrome
(complications, diagnosis, drug therapy)
- Treatment Outcome
|