Acute Aseptic Meningitis Temporally Associated with Intravenous Polyclonal Immunoglobulin Therapy: A Systematic Review.
Elisabetta L T De FeliceGabriel F TotiBeatrice GattiRenato GualtieriPietro CamozziSebastiano A G LavaGregorio P MilaniGiorgio TregliaFederica VanoniMario G BianchettiGianmaria F BernasconiBenedetta Terziroli Beretta PiccoliCamilla LavagnoPublished in: Clinical reviews in allergy & immunology (2024)
An acute aseptic meningitis has been occasionally observed on intravenous polyclonal human immunoglobulin therapy. Since case reports cannot be employed to draw inferences about the relationships between immunoglobulin therapy and meningitis, we conducted a systematic review and meta-analysis of the literature. Eligible were cases, case series, and pharmacovigilance studies. We found 71 individually documented cases (36 individuals ≤ 18 years of age) of meningitis. Ninety percent of cases presented ≤ 3 days after initiating immunoglobulin therapy and recovered within ≤ 7 days (with a shorter disease duration in children: ≤ 3 days in 29 (94%) cases). In 22 (31%) instances, the authors noted a link between the onset of meningitis and a rapid intravenous infusion of immunoglobulins. Cerebrospinal fluid analysis revealed a predominantly neutrophilic (N = 46, 66%) pleocytosis. Recurrences after re-exposure were observed in eight (N = 11%) patients. Eight case series addressed the prevalence of meningitis in 4089 patients treated with immunoglobulins. A pooled prevalence of 0.6% was noted. Finally, pharmacovigilance data revealed that meningitis temporally associated with intravenous immunoglobulin therapy occurred with at least five different products. In conclusion, intravenous immunoglobulin may cause an acute aseptic meningitis. The clinical features remit rapidly after discontinuing the medication.
Keyphrases
- cerebrospinal fluid
- high dose
- liver failure
- drug induced
- risk factors
- healthcare
- systematic review
- respiratory failure
- emergency department
- randomized controlled trial
- young adults
- end stage renal disease
- cell therapy
- adverse drug
- hepatitis b virus
- mesenchymal stem cells
- bone marrow
- acute respiratory distress syndrome
- smoking cessation
- electronic health record
- artificial intelligence
- quantum dots
- patient reported outcomes
- african american