Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 1994 Jul;97 Suppl 1(Suppl 1):69-72.

Polyclonal intravenous immune globulin for prevention and treatment of infections in critically ill patients

Affiliations
Review

Polyclonal intravenous immune globulin for prevention and treatment of infections in critically ill patients

A Cometta et al. Clin Exp Immunol. 1994 Jul.

Abstract

Infections remain the leading cause of death among patients admitted to intensive care units (ICU). Infections due to Gram-negative bacteria are both frequent and difficult to treat. The poor outcome of such infections has been attributed to the endotoxin. The high mortality rate related to Gram-negative sepsis has prompted the testing of new, adjunctive therapies to prevent and treat infections in critically ill patients. Immunotherapy or immunoprophylaxis have long been investigated in this context. Passive immunotherapy consists of the administration of immune plasma or serum, or standard or hyperimmune purified immune globulins. Several clinical studies using such preparations to treat critically ill patients are reviewed in this article. While two studies using hyperimmune plasma or serum appeared to be successful, two studies using hyperimmune globulin failed to show a beneficial effect in the treatment or the prevention of Gram-negative septic shock. Regarding the infusion of standard intravenous immune globulin (IVIG) two studies have demonstrated a substantial benefit in the prevention of severe infections; the reduction of nosocomial pneumonia recorded in both trials and the shortness of stay in ICU may also afford savings in hospital costs. The cost effectiveness of such prophylactic administration of IVIG is worthy of further investigation.

PubMed Disclaimer

Similar articles

Cited by

References

    1. J Immunol. 1972 Mar;108(3):601-10 - PubMed
    1. Immunobiology. 1993 Apr;187(3-5):464-77 - PubMed
    1. Trans Assoc Am Physicians. 1975;88:101-8 - PubMed
    1. J Infect Dis. 1977 Aug;136 Suppl:S167-73 - PubMed
    1. J Exp Med. 1978 Apr 1;147(4):1007-17 - PubMed

MeSH terms

Substances

LinkOut - more resources