2017
DOI: 10.1002/ajh.24644
|View full text |Cite
|
Sign up to set email alerts
|

Association of immune globulin intravenous and thromboembolic adverse events

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
7
0
1

Year Published

2017
2017
2024
2024

Publication Types

Select...
8

Relationship

0
8

Authors

Journals

citations
Cited by 10 publications
(8 citation statements)
references
References 4 publications
0
7
0
1
Order By: Relevance
“…Additional immunosuppressive agents and apheresis with albumin replacement may not be necessary. It may be prudent to avoid IVIg because its efficacy is unknown and adverse reactions to IVIg may mimic the thrombotic, 12 neurologic, 13 and renal 14 manifestations of TTP.…”
Section: Resultsmentioning
confidence: 99%
“…Additional immunosuppressive agents and apheresis with albumin replacement may not be necessary. It may be prudent to avoid IVIg because its efficacy is unknown and adverse reactions to IVIg may mimic the thrombotic, 12 neurologic, 13 and renal 14 manifestations of TTP.…”
Section: Resultsmentioning
confidence: 99%
“…An electrocardiogram demonstration right axis deviation, troponin-I was newly detectable at 0.06 ng/mL and Bnatriuretic peptide (BNP) increased to 1617 pg/mL. She Due to concern for inflammatory multi-system organ involvement similar to that seen in MIS-C, and risk of progression to more florid cardiac involvement, a riskbenefit discussion was held with the patient regarding treatment with intravenous immunoglobulin (IVIG), including potential risk of hypercoagulability [6]. She was treated with IVIG 2 g/kg split equally between hospital days 2 and 3 to reduce risk for thromboembolic and renal toxicities, along with aspirin 325 mg daily for 7 days, based on treatment courses suggested for pediatric patients with MIS-C or Kawasaki disease [7][8][9].…”
Section: Case Presentationmentioning
confidence: 99%
“…To date, evidence from controlled trials has been conflicting as to their success in severe COVID-19, and treatment is not given based on hyperinflammation [178,179]. Due to the current paucity of supporting evidence and risk of thromboembolic events associated with IVIG therapy, especially due to reports of hypercoagulability in severe COVID-19, IVIG, hyperimmune globulin, and convalescent plasma remain investigational [1,180].…”
Section: Intravenous Immunoglobulin (Ivig)mentioning
confidence: 99%