A controlled trial of intravenous immune globulin for the prevention of serious bacterial infections in children receiving zidovudine for advanced human immunodeficiency virus infection. Pediatric AIDS Clinical Trials Group. 1994

S A Spector, and R D Gelber, and N McGrath, and D Wara, and A Barzilai, and E Abrams, and Y J Bryson, and W M Dankner, and R A Livingston, and E M Connor
University of California, San Diego, La Jolla 92093-0672.

BACKGROUND Serious bacterial infections are common in children infected with the human immunodeficiency virus (HIV). Studies performed before zidovudine became standard therapy found that intravenous immune globulin decreases the number of serious bacterial infections in these children. We designed a multicenter study to evaluate the efficacy of intravenous immune globulin in children with advanced HIV infection who were receiving zidovudine. METHODS In a double-blind trial 255 children between 3 months and 12 years of age who had the acquired immunodeficiency syndrome (AIDS) or AIDS-related complex were randomly assigned to receive either intravenous immune globulin (400 mg per kilogram of body weight) (n = 129) or placebo (0.1 percent albumin) (n = 126) every 28 days. All children received 180 mg of zidovudine per square meter of body-surface area orally four times daily. Treatment assignment was stratified according to whether the patients had a history of one or more serious bacterial infections, had previously been treated with zidovudine, or were currently receiving prophylaxis with trimethoprim-sulfamethoxazole. The median length of follow-up was 30.6 months. RESULTS The estimated two-year rates of serious bacterial infections with confirmed pathogens were 16.9 percent for the immune globulin group and 24.3 percent for the placebo group (relative risk, 0.60; 95 percent confidence interval, 0.35 to 1.04; P = 0.07). The treatment effect was seen primarily among the 174 children who were not receiving trimethoprim-sulfamethoxazole prophylaxis at entry; the estimated two-year rates of infection were 11.3 percent for the immune globulin group and 26.8 percent for the placebo group (relative risk, 0.45; 95 percent confidence interval, 0.22 to 0.91; P = 0.03). For the 81 children who were receiving trimethoprim-sulfamethoxazole prophylaxis initially, the rates were 27.7 percent in the immune globulin group and 17.7 percent in the placebo group (relative risk, 1.26; 95 percent confidence interval, 0.44 to 3.66; P = 0.67). The two-year survival was similar in the two groups: 79.2 percent among immune globulin recipients and 75.4 percent among placebo recipients (P = 0.41). CONCLUSIONS In children with advanced HIV disease who are receiving zidovudine, intravenous immune globulin decreases the risk of serious bacterial infections. However, this benefit is apparent only in children who are not receiving trimethoprim-sulfamethoxazole as prophylaxis.

UI MeSH Term Description Entries
D007223 Infant A child between 1 and 23 months of age. Infants
D008297 Male Males
D011379 Prognosis A prediction of the probable outcome of a disease based on a individual's condition and the usual course of the disease as seen in similar situations. Prognostic Factor,Prognostic Factors,Factor, Prognostic,Factors, Prognostic,Prognoses
D002648 Child A person 6 to 12 years of age. An individual 2 to 5 years old is CHILD, PRESCHOOL. Children
D002675 Child, Preschool A child between the ages of 2 and 5. Children, Preschool,Preschool Child,Preschool Children
D004311 Double-Blind Method A method of studying a drug or procedure in which both the subjects and investigators are kept unaware of who is actually getting which specific treatment. Double-Masked Study,Double-Blind Study,Double-Masked Method,Double Blind Method,Double Blind Study,Double Masked Method,Double Masked Study,Double-Blind Methods,Double-Blind Studies,Double-Masked Methods,Double-Masked Studies,Method, Double-Blind,Method, Double-Masked,Methods, Double-Blind,Methods, Double-Masked,Studies, Double-Blind,Studies, Double-Masked,Study, Double-Blind,Study, Double-Masked
D005260 Female Females
D005500 Follow-Up Studies Studies in which individuals or populations are followed to assess the outcome of exposures, procedures, or effects of a characteristic, e.g., occurrence of disease. Followup Studies,Follow Up Studies,Follow-Up Study,Followup Study,Studies, Follow-Up,Studies, Followup,Study, Follow-Up,Study, Followup
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000163 Acquired Immunodeficiency Syndrome An acquired defect of cellular immunity associated with infection by the human immunodeficiency virus (HIV), a CD4-positive T-lymphocyte count under 200 cells/microliter or less than 14% of total lymphocytes, and increased susceptibility to opportunistic infections and malignant neoplasms. Clinical manifestations also include emaciation (wasting) and dementia. These elements reflect criteria for AIDS as defined by the CDC in 1993. AIDS,Immunodeficiency Syndrome, Acquired,Immunologic Deficiency Syndrome, Acquired,Acquired Immune Deficiency Syndrome,Acquired Immuno-Deficiency Syndrome,Acquired Immuno Deficiency Syndrome,Acquired Immuno-Deficiency Syndromes,Acquired Immunodeficiency Syndromes,Immuno-Deficiency Syndrome, Acquired,Immuno-Deficiency Syndromes, Acquired,Immunodeficiency Syndromes, Acquired,Syndrome, Acquired Immuno-Deficiency,Syndrome, Acquired Immunodeficiency,Syndromes, Acquired Immuno-Deficiency,Syndromes, Acquired Immunodeficiency

Related Publications

S A Spector, and R D Gelber, and N McGrath, and D Wara, and A Barzilai, and E Abrams, and Y J Bryson, and W M Dankner, and R A Livingston, and E M Connor
January 1996, Archives of internal medicine,
S A Spector, and R D Gelber, and N McGrath, and D Wara, and A Barzilai, and E Abrams, and Y J Bryson, and W M Dankner, and R A Livingston, and E M Connor
July 1991, The New England journal of medicine,
S A Spector, and R D Gelber, and N McGrath, and D Wara, and A Barzilai, and E Abrams, and Y J Bryson, and W M Dankner, and R A Livingston, and E M Connor
August 1992, The New England journal of medicine,
S A Spector, and R D Gelber, and N McGrath, and D Wara, and A Barzilai, and E Abrams, and Y J Bryson, and W M Dankner, and R A Livingston, and E M Connor
January 1993, Pediatric research,
S A Spector, and R D Gelber, and N McGrath, and D Wara, and A Barzilai, and E Abrams, and Y J Bryson, and W M Dankner, and R A Livingston, and E M Connor
April 1995, American journal of health-system pharmacy : AJHP : official journal of the American Society of Health-System Pharmacists,
S A Spector, and R D Gelber, and N McGrath, and D Wara, and A Barzilai, and E Abrams, and Y J Bryson, and W M Dankner, and R A Livingston, and E M Connor
June 1997, The Pediatric infectious disease journal,
S A Spector, and R D Gelber, and N McGrath, and D Wara, and A Barzilai, and E Abrams, and Y J Bryson, and W M Dankner, and R A Livingston, and E M Connor
December 1999, Obstetrics and gynecology,
S A Spector, and R D Gelber, and N McGrath, and D Wara, and A Barzilai, and E Abrams, and Y J Bryson, and W M Dankner, and R A Livingston, and E M Connor
April 1996, The New England journal of medicine,
S A Spector, and R D Gelber, and N McGrath, and D Wara, and A Barzilai, and E Abrams, and Y J Bryson, and W M Dankner, and R A Livingston, and E M Connor
March 1995, The New England journal of medicine,
S A Spector, and R D Gelber, and N McGrath, and D Wara, and A Barzilai, and E Abrams, and Y J Bryson, and W M Dankner, and R A Livingston, and E M Connor
February 1998, Pediatrics,
Copied contents to your clipboard!