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Duration of Response to Intramuscular Versus Low Dose Intradermal Hepatitis B Booster Immunization

Published online by Cambridge University Press:  21 June 2016

W. Paul McKinney ,
Susan K. Russler ,
Mary M. Horowitz ,
Richard J. Battiola  and
Martha Bi-Fong Lee
W. Paul McKinney*
Affiliation:
Divisions of General Internal Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin Infectious Diseases, Medical College of Wisconsin, Milwaukee, Wisconsin
Susan K. Russler
Affiliation:
Infectious Diseases, Medical College of Wisconsin, Milwaukee, Wisconsin
Mary M. Horowitz
Affiliation:
Divisions of General Internal Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin
Richard J. Battiola
Affiliation:
Divisions of General Internal Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin
Martha Bi-Fong Lee
Affiliation:
Division of Biostatistics and Clinical Epidemiology, Medical College of Wisconsin, Milwaukee, Wisconsin
*
Medical Service (111), Dallas VA Medical Center, 4500 South Lancaster Road, Dallas, TX 75216
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Abstract

Objective:

To determine the duration of the immune response to plasma-derived hepatitis B vaccine among healthcare workers responding to booster doses of intradermal (ID) or intramuscular (IM) vaccine in 1986 and those with protective levels of antibody to hepatitis B surface antigen (anti-HBs) in 1986 without booster vaccine. Both groups received a primary hepatitis B vaccine series 24 to 36 months earlier.

Design:

Cross-sectional follow-up study two years later of an inception cohort defined in 1986.

Setting:

An academically affiliated metropolitan county hospital.

Participants:

Group 1: Hospital employees responding to booster doses of hepatitis B vaccine given ID or IM in 1986 due to low anti-HBs levels. Forty-one (82%) of 50 eligible persons were evaluated. Group 2: Persons not receiving booster vaccine in 1986 due to protective levels of anti-HBs. A random sample of 95 persons was drawn from a pool of 152 participants with protective levels in 1986. sixty-five (68%) of 95 contacted persons were restudied.

Results:

In 1988, 14 (64%) of 22 previous ID responders had anti-HBs levels ≥ 10 milli-international units (mIU)/mL, compared with 17 (89%) of 19 IM responders (p= .055). The 1988 geometric mean titer of IM recipients was 66.4 ±4.5 mIU/mL and of ID recipients was 20.7 ±7.4 (p= .04). None of 65 Group 2 subjects' anti-HBs titers dropped below 10 mIU/mL by 1988.

Conclusions:

plasma-derived hepatitis B vaccine recipients with anti-HBs levels ≥ 10 mIU/mL at 24 to 36 months after primary immunization are likely to maintain these levels two years later. The diminished durability of the antibody response together with the increased rate of local side effects associated with the ID injection route may limit its applicability as an alternative to using IM booster doses of hepatitis B vaccine.

Type
Original Articles
Information
Infection Control & Hospital Epidemiology , Volume 12 , Issue 4 , April 1991 , pp. 226 - 230
Copyright
Copyright © The Society for Healthcare Epidemiology of America 1991

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