2031. False-positive Serologic Results attributable to IVIG therapy. (26th November 2018)
- Record Type:
- Journal Article
- Title:
- 2031. False-positive Serologic Results attributable to IVIG therapy. (26th November 2018)
- Main Title:
- 2031. False-positive Serologic Results attributable to IVIG therapy
- Authors:
- Hanson, Kimberly E
Gabriel, Nielsen
Mchardy, Ian
Hoffmann, Wesley
Cohen, Stuart H
Welch, Ryan
Couturier, Marc Roger
Thompson, George R - Abstract:
- Abstract: Background: Intravenous immunoglobulin (IVIG) is used to treat an increasing number of conditions including hematologic, rheumatologic and immunodeficiency diseases. The immunomodulatory effects can be life-saving, however recent administration can complicate diagnostics when patients later present with symptoms necessitating serologic testing. We evaluated the serologic profile of IVIG for commonly ordered infectious diseases serologies. Methods: Patients were enrolled if they received and were naïve to IVIG therapy. Blood was drawn prior to IVIG and 72–96 hours post-infusion. All samples were tested for: Bartonella, Coccidioides, Brucella, Histoplasma, Coxiella, West Nile, St. Louis, California, Eastern, and Western Encephalitis, Lyme, Dengue, HSV 1 and 2, Chikungunya, cytomegalovirus, varicella zoster, Epstein-Barr and Toxoplasma by standard methodologies (ARUP, Salt Lake City, UT). Pre- and post-infusion antibody concentrations were evaluated to determine the potential false-positive rate of serologic testing. Results: Seven patients received IVIG (renal transplant rejection, two patients; Guillain–Barre syndrome, three patients; bone marrow transplant, two patients). Six of seven patients receiving IVIG had at least one evaluated serology become positive 72 hours after IVIG infusion. Antibodies for CMV, HSV-2, and EBV early antigen D turned positive in three patients. Antibodies for WNV, Coccidioides IgG, and Histoplasma yeast IgG became positive in twoAbstract: Background: Intravenous immunoglobulin (IVIG) is used to treat an increasing number of conditions including hematologic, rheumatologic and immunodeficiency diseases. The immunomodulatory effects can be life-saving, however recent administration can complicate diagnostics when patients later present with symptoms necessitating serologic testing. We evaluated the serologic profile of IVIG for commonly ordered infectious diseases serologies. Methods: Patients were enrolled if they received and were naïve to IVIG therapy. Blood was drawn prior to IVIG and 72–96 hours post-infusion. All samples were tested for: Bartonella, Coccidioides, Brucella, Histoplasma, Coxiella, West Nile, St. Louis, California, Eastern, and Western Encephalitis, Lyme, Dengue, HSV 1 and 2, Chikungunya, cytomegalovirus, varicella zoster, Epstein-Barr and Toxoplasma by standard methodologies (ARUP, Salt Lake City, UT). Pre- and post-infusion antibody concentrations were evaluated to determine the potential false-positive rate of serologic testing. Results: Seven patients received IVIG (renal transplant rejection, two patients; Guillain–Barre syndrome, three patients; bone marrow transplant, two patients). Six of seven patients receiving IVIG had at least one evaluated serology become positive 72 hours after IVIG infusion. Antibodies for CMV, HSV-2, and EBV early antigen D turned positive in three patients. Antibodies for WNV, Coccidioides IgG, and Histoplasma yeast IgG became positive in two patients.Finally, antibodies for HSV-1 and -2, and EBV nuclear antigen each turned positive in one patient. Patients received between 20 and 112.5 g. Of the three patients who received more than 100 g of IVIG, two had at least four serologies turn positive. Of the patients who received <100 g (20–50 g), none had >3 turn positive ( P < 0.05). One patient had three serologies turn negative ( Coccidioides, HSV 2, and EBV Early D) after infusion of 36.5 g of IVIG, with none turning positive. Conclusion: Use of IVIG has increased significantly over the past decade; however, the potential pitfalls in serologic diagnostics associated with receipt of IVIG have not been studied systematically and is likely a confounder in serologic diagnostics causing both false-positive and false-negative results. We found a number of screening and diagnostic serologies can be artificially altered after infusion of IVIG. Disclosures: All authors: No reported disclosures. … (more)
- Is Part Of:
- Open forum infectious diseases. Volume 5(2018)Supplement 1
- Journal:
- Open forum infectious diseases
- Issue:
- Volume 5(2018)Supplement 1
- Issue Display:
- Volume 5, Issue 1 (2018)
- Year:
- 2018
- Volume:
- 5
- Issue:
- 1
- Issue Sort Value:
- 2018-0005-0001-0000
- Page Start:
- S591
- Page End:
- S592
- Publication Date:
- 2018-11-26
- Subjects:
- Communicable diseases -- Periodicals
Medical microbiology -- Periodicals
Infection -- Periodicals
616.9 - Journal URLs:
- http://ofid.oxfordjournals.org/ ↗
http://www.oxfordjournals.org/en/ ↗ - DOI:
- 10.1093/ofid/ofy210.1687 ↗
- Languages:
- English
- ISSNs:
- 2328-8957
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 21963.xml