Immunoprophylaxis against Klebsiella and Pseudomonas aeruginosa Infections
Author(s) -
Sam T. Donta,
Peter Peduzzi,
Alan S. Cross,
Jerald Sadoff,
Clair Haakenson,
Stanley J. Cryz,
Christopher A. Kauffman,
Suzanne Bradley,
G D Gafford,
D. Elliston,
Thomas R. Beam,
Jamie John,
Bruce S. Ribner,
Robert Cantey,
Ceri Welsh,
Richard T. Ellison,
Edward J. Young,
Richard J. Hamill,
Howard L. Leaf,
R. M. H. Schein,
Maury E. Mulligan,
Cheilonda Johnson,
Elías Abrutyn,
J. McLeod Griffiss,
Randa Hamadeh,
Arn H. Eliasson,
J. Bruce McClain,
G. P. Melcher,
Jonathan W. Kelly,
W. R. Byrne,
Meghan A. Wallace,
Dennis Amundson,
Brunhilde Gumpert,
D. Slagle,
Federal Hyperimmune Immunoglobulin Trial Study Group
Publication year - 1996
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1093/infdis/174.3.537
Subject(s) - pseudomonas aeruginosa , microbiology and biotechnology , klebsiella , klebsiella pneumoniae , medicine , virology , biology , bacteria , escherichia coli , biochemistry , gene , genetics
To determine if passive immunization could decrease the incidence or severity of Klebsiella and Pseudomonas aeruginosa infections, patients admitted to intensive care units of 16 Department of Veterans Affairs and Department of Defense hospitals were randomized to receive either 100 mg/kg intravenous hyperimmune globulin (IVIG), derived from donors immunized with a 24-valent Klebsiella capsular polysaccharide plus an 8-valent P. aeruginosa O-polysaccharide-toxin A conjugate vaccine, or an albumin placebo. The overall incidence and severity of vaccine-specific Klebsiella plus Pseudomonas infections were not significantly different between the groups receiving albumin and IVIG. There was some evidence that IVIG may decrease the incidence (2.7% albumin vs. 1.2% IVIG) and severity (1.0% vs. 0.3%) of vaccine-specific Klebsiella infections, but these reductions were not statistically significant. The trial was stopped because it was statistically unlikely that IVIG would be protective against Pseudomonas infections at the dosage being used. Patients receiving IVIG had more adverse reactions (14.4% vs. 9.2%).
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