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Response to vaccination against hepatitis B virus with a schedule of four 40-μg doses in cirrhotic patients evaluated for liver transplantation: factors associated with a response.
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- Author(s): Gutierrez Domingo I;Gutierrez Domingo I; Pascasio Acevedo JM; Alcalde Vargas A; Ramos Cuadra A; Ferrer Ríos MT; Sousa Martin JM; Sayago Mota M; Giráldez Gallego A; Suárez Artacho G
- Source:
Transplantation proceedings [Transplant Proc] 2012 Jul-Aug; Vol. 44 (6), pp. 1499-501.- Publication Type:
Journal Article- Language:
English - Source:
- Additional Information
- Source: Publisher: Elsevier Science Inc Country of Publication: United States NLM ID: 0243532 Publication Model: Print Cited Medium: Internet ISSN: 1873-2623 (Electronic) Linking ISSN: 00411345 NLM ISO Abbreviation: Transplant Proc Subsets: MEDLINE
- Publication Information: Publication: New York, N.Y. : Elsevier Science Inc.
Original Publication: New York Stratton. - Subject Terms: Liver Transplantation*/adverse effects ; Vaccination*; Hepatitis B/*prevention & control ; Hepatitis B Vaccines/*administration & dosage ; Hepatitis B virus/*immunology ; Liver Cirrhosis/*surgery; Adolescent ; Adult ; Aged ; Chi-Square Distribution ; Female ; Hepatitis B/blood ; Hepatitis B/diagnosis ; Hepatitis B Antibodies/blood ; Hepatitis B Surface Antigens/blood ; Humans ; Immunization Schedule ; Injections, Intramuscular ; Liver Cirrhosis/diagnosis ; Logistic Models ; Male ; Middle Aged ; Multivariate Analysis ; Odds Ratio ; Retrospective Studies ; Severity of Illness Index ; Spain ; Time Factors ; Treatment Outcome ; Young Adult
- Abstract: We performed a retrospective study to evaluate the rate of and factors associated with a response to recombinant hepatitis B virus (HBV) vaccination using 4 intramuscular doses (40 μg) administered at 0, 1, 2, and 6 months among 278 cirrhotic patients being evaluated for orthotopic liver transplantation (OLT). We re-vaccinated 57 non-responders with the same schedule. The 39.2% overall response rate to vaccination included 36% after three and 40.7% after four doses, namely, a median anti-HBs level of 100 IU/mL (range, 10 to 1000 IU/mL). The 51% revaccination response rate achieved a median hepatitis B surface antibody (anti-HBs) level of 99 IU/mL (range, 11 to >1000 IU/mL). Upon univariate analysis, variables associated with a higher response were: better liver function (Child-Pugh class [A, 53.8% B, 33.3%, C, 30.1%; P = .002), Model for End-stage Liver-Disease (MELD) score (11.4 versus 13.6; P = .001]), absence of diabetes (43.6% versus 20.8%; P = .002), presence of isolated hepatitis B core antibody (anti-HBc) positivity (80% versus 37.7%; P = .007), and younger age (< 45 years, 52.2%; range, 45 to 55 years, 40.4%; > 55 years, 34.1%; P = .031). Upon multivariate logistic regression analysis, lower MELD score (odds ratio [OR]: 0.922; P = .046), absence of diabetes (OR:0.359; P = .008) and isolated anti-HBc positivity (OR:5.826; P = .034) were associated with a higher response. No differences were observed to be associated with gender, weight, body mass index, etiology or tobacco consumption. Among the same patient cohort (n = 79), the responses after the third and fourth doses were 36.7% and 51.9% respectively. In conclusion, the response rate to HBV vaccination in cirrhotic patients evaluated for OLT reached more than 35% among those who received at least 3 doses. It was higher among patients who showed isolated anti-HBc positivity, better liver function, younger age, and non-diabetic status. The fourth dose only increased the response rate by 24% over that obtained after the first three doses, whereas a revaccination achieved a 50% response rate, which probably accounts for revaccination after no response to 3 doses. Vaccination should be introduced against HBV in the early stages of the disease.
(Copyright © 2012 Elsevier Inc. All rights reserved.) - Accession Number: 0 (Hepatitis B Antibodies)
0 (Hepatitis B Surface Antigens)
0 (Hepatitis B Vaccines) - Publication Date: Date Created: 20120731 Date Completed: 20130103 Latest Revision: 20120730
- Publication Date: 20221213
- Accession Number: 10.1016/j.transproceed.2012.05.071
- Accession Number: 22841195
- Source:
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