| Literature DB >> 29771873 |
Aaron M Harris, Ruth Link-Gelles, Karen Kim, Edwin Chandrasekar, Su Wang, Nicole Bannister, Perry Pong, Eric Chak, Moon S Chen, Christopher Bowlus, Noele P Nelson.
Abstract
Among an estimated 850,000 to 2.2 million persons with chronic hepatitis B virus (HBV) infection in the United States, 70% are non-U.S.-born (1,2). All patients require linkage to care, and approximately 20%-40% require antiviral treatment (3). Without treatment, one in four persons chronically infected with HBV will die prematurely from liver failure, liver cirrhosis, or hepatocellular carcinoma (4). To mitigate morbidity and mortality, CDC funded a cooperative agreement to develop hepatitis B testing and linkage-to-care programs serving non-U.S.-born persons during October 2014-September 2017. This report describes each program's operational services and partnerships with primary care centers, community-based organizations, and public health departments to recruit non-U.S.-born persons for HBV testing using the hepatitis B surface antigen (HBsAg) and link those whose test results were positive to HBV-directed care (medical visit attendance with monitoring of HBV DNA and liver enzyme tests). Among 10,152 program participants, 757 (7.5%) were HBsAg-positive, indicative of chronic HBV infection; among these, 643 (85%) attended ≥1 medical visit, 587 (78%) received HBV-directed care, and 137 (18%) were prescribed antiviral treatment. Among 273 household contacts of HBsAg-positive persons, 39 (14%) had positive test results for HBsAg. Prevalence of current HBV infection was high in this non-U.S.-born population and among household and sexual contacts of HBV-infected persons. HBV testing and linkage to care can be achieved through partnerships with community organizations, health centers, and public health departments.Entities:
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Year: 2018 PMID: 29771873 PMCID: PMC6048941 DOI: 10.15585/mmwr.mm6719a2
Source DB: PubMed Journal: MMWR Morb Mortal Wkly Rep ISSN: 0149-2195 Impact factor: 17.586
Percentage of HBsAg-positive persons participating in three programs to increase hepatitis B testing and linkage to care are who received HBV-directed care* and treatment, by demographic characteristics — Sacramento, California; Livingston, New Jersey and New York City, New York; and Chicago, Illinois, October 2014–September 2017
| Demographic characteristic | HBsAg–positive | Received HBV–directed care* | Prescribed antiviral | ||
|---|---|---|---|---|---|
| No. (% of total) | No. (%) | Unadjusted OR (95% CI) | No. (%) | Unadjusted OR (95% CI) | |
|
| 757 (100) | 587 (78) | N/A | 137 (18) | N/A |
|
| |||||
| Female | 344 (45) | 276 (80) | Referent | 50 (15) | Referent |
| Male | 413 (55) | 349 (85) | 1.3 (0.9–1.8) | 87 (21) | 1.6 (1.1–2.4) |
|
| |||||
| <50 | 518 (68) | 423 (82) | Referent | 83 (16) | Referent |
| 239 (32) | 164 (69) | 0.5 (0.3–0.7) | 54 (23) | 2.0 (1.4–3.0) | |
|
| |||||
| White | 17 (2) | 14 (82) | Referent | 2 (12) | Referent |
| Black/African | 122 (16) | 83 (68) | 0.5 (0.1–1.7) | 7 (6) | 2.3 (0.5–10.4) |
| Asian | 602 (80) | 474 (79) | 0.8 (0.2–2.8) | 122 (20) | 0.5 (0.1–2.4) |
| Native American/Pacific Islander | 3 (0) | 3 (100) | —† | 1 (33) | 3.8 (0.2–62.8) |
| Other/Unknown | 13 (2) | 13 (100) | —† | 5 (38) | —† |
|
| |||||
| None | 121 (16) | 68 (56) | 0.3 (0.2–0.4) | 19 (16) | 0.9 (0.5–1.7) |
| Private | 210 (28) | 174 (83) | Referent | 41 (20) | Referent |
| Public | 334 (44) | 289 (87) | 1.3 (0.8–2.1) | 56 (17) | 0.8 (0.5–1.3) |
| Missing | 92 (12) | 56 (61) | N/A | 21 (23) | N/A |
|
| |||||
| English | 229 (30) | 178 (78) | 1.0 (0.7–1.4) | 52 (23) | 1.4 (0.9–2.0) |
| Not English (yes to any other language) | 520 (69) | 406 (78) | Referent | 84 (16) | Referent |
| Missing | 8 (1) | 3 (38) | N/A | 1 (13) | N/A |
|
| |||||
| U.S.-born | 16 (2) | 13 (81) | 1.3 (0.4–4.5) | 3 (19) | 1.2 (0.3–4.3) |
| Non–U.S.-born | 732 (97) | 567 (77) | Referent | 133 (18) | Referent |
| Missing | 9 (1) | 7 (78) | N/A | 1 (11) | N/A |
|
| |||||
| Cirrhosis (vs. no cirrhosis) | 18 (2) | 17 (94) | 1.3 (0.1–9.9) | 14 (78) | 13.1 (4.2–40.6) |
| HCC (vs. no HCC) | 9 (1) | 9 (100) | —† | 7 (78) | 24.6 (3.0–202.4) |
| Neither cirrhosis nor HCC | 469 (62) | 439 (94) | N/A | 98 (21) | N/A |
| Missing | 264 (35) | 128 (48) | N/A | 24 (9) | N/A |
|
| |||||
| Family history of HBV (vs. no family history of HBV) | 190 (25) | 158 (83) | 1.1 (0.7–1.7) | 45 (24) | 1.7 (1.1–2.7) |
| Family history of HCC (vs. no family history of HCC) | 66 (9) | 53 (80) | 0.9 (0.5–1.7) | 20 (30) | 2.2 (1.2–4.0) |
| No family history of HBV/HCC | 364 (48) | 303 (83) | N/A | 59 (16) | N/A |
| Missing | 182 (24) | 111 (61) | N/A | 29 (16) | N/A |
|
| |||||
| No risk factors reported | 485 (64) | 409 (84) | Referent | 82 (17) | Referent |
| At least one risk factor§ reported | 139 (18) | 124 (89) | 1.5 (0.9–2.8) | 37 (27) | 1.8 (1.1–2.7) |
| No risk factor data available | 133 (18) | 54 (41) | N/A | 18 (14) | N/A |
Abbreviations: CI = confidence interval; HBsAg = hepatitis B surface antigen; HBV = hepatitis B virus; HCC = hepatocellular carcinoma; N/A = not applicable; OR = odds ratio.
* Received testing for hepatitis B e antigen, hepatitis B virus DNA, and alanine transaminase.
† Insufficient cell size to calculate OR.
§ Injection drug use, men who have sex with men, household contact, sexual contact, multiple sex partners, human immunodeficiency virus–positive.
FIGUREHepatitis B linkage-to-care continuum* — three U.S. programs, October 2014–September 2017
Abbreviation: HBsAg = hepatitis B surface antigen.
* Stages in care continuum are the following: linked to care = attended >1 medical visit; engaged in care = received hepatitis B e antigen, hepatitis B virus DNA, and alanine transaminase testing; retained in care = attended >2 medical visits; prescribed antiviral = given treatment with antiviral (approximately 20%–40% of patients with chronic hepatitis B virus infection require treatment).