A Comparison Between Community and Academic Practices in the USA in the Management of Chronic Hepatitis B Patients Receiving Entecavir: Results of the ENUMERATE Study.


Journal

Digestive diseases and sciences
ISSN: 1573-2568
Titre abrégé: Dig Dis Sci
Pays: United States
ID NLM: 7902782

Informations de publication

Date de publication:
02 2019
Historique:
received: 12 06 2018
accepted: 07 09 2018
pubmed: 22 9 2018
medline: 26 3 2019
entrez: 22 9 2018
Statut: ppublish

Résumé

The management of chronic hepatitis B patients is not well characterized in real-world practice. We compared baseline characteristics of CHB patients on entecavir, the frequency of on-treatment monitoring, and the effectiveness of ETV treatment between academic and community practices. Treatment-naïve CHB patients ≥18 years old, treated with ETV for ≥12 months from 2005 to 2013, in 26 community and academic practices throughout the USA were retrospectively evaluated. Of 841 patients enrolled, 658 (65% male, 83% Asian, median age 47, 9% with cirrhosis) met inclusion criteria. Half of the patients (52%) were from community practices. A lower percentage of patients in community practices had cirrhosis or liver cancer (5 vs. 14%). Community practices more often treated patients with baseline ALT < 2 × ULN. Over a median follow-up of 4 years, community practices were more likely to discontinue ETV with less frequent laboratory monitoring compared to academic practices. The 5-year cumulative probability of ALT normalization was greater among patients treated in community practices (70 vs. 50%, p < 0.001), but the 5-year cumulative probability of undetectable HBV DNA was lower (45 vs. 70%, p < 0.001) than those treated in academic practices. Academic practices saw CHB patients with more advanced liver disease, more often followed AASLD guidelines, and monitored patients on ETV treatment more frequently than community practices. While patients in community practices were less likely to achieve undetectable HBV DNA and more likely to achieve ALT normalization, the rates of HBeAg loss and seroconversion as well as HBsAg loss were similar.

Sections du résumé

BACKGROUND AND AIMS
The management of chronic hepatitis B patients is not well characterized in real-world practice. We compared baseline characteristics of CHB patients on entecavir, the frequency of on-treatment monitoring, and the effectiveness of ETV treatment between academic and community practices.
METHODS
Treatment-naïve CHB patients ≥18 years old, treated with ETV for ≥12 months from 2005 to 2013, in 26 community and academic practices throughout the USA were retrospectively evaluated.
RESULTS
Of 841 patients enrolled, 658 (65% male, 83% Asian, median age 47, 9% with cirrhosis) met inclusion criteria. Half of the patients (52%) were from community practices. A lower percentage of patients in community practices had cirrhosis or liver cancer (5 vs. 14%). Community practices more often treated patients with baseline ALT < 2 × ULN. Over a median follow-up of 4 years, community practices were more likely to discontinue ETV with less frequent laboratory monitoring compared to academic practices. The 5-year cumulative probability of ALT normalization was greater among patients treated in community practices (70 vs. 50%, p < 0.001), but the 5-year cumulative probability of undetectable HBV DNA was lower (45 vs. 70%, p < 0.001) than those treated in academic practices.
CONCLUSION
Academic practices saw CHB patients with more advanced liver disease, more often followed AASLD guidelines, and monitored patients on ETV treatment more frequently than community practices. While patients in community practices were less likely to achieve undetectable HBV DNA and more likely to achieve ALT normalization, the rates of HBeAg loss and seroconversion as well as HBsAg loss were similar.

Identifiants

pubmed: 30238203
doi: 10.1007/s10620-018-5281-3
pii: 10.1007/s10620-018-5281-3
doi:

Substances chimiques

Antiviral Agents 0
DNA, Viral 0
Hepatitis B Surface Antigens 0
Hepatitis B e Antigens 0
entecavir 5968Y6H45M
Guanine 5Z93L87A1R
Alanine Transaminase EC 2.6.1.2

Types de publication

Comparative Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

358-366

Commentaires et corrections

Type : CommentIn

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Auteurs

Hannah M Lee (HM)

Division of Gastroenterology, Hepatology and Nutrition, Virginia Commonwealth University Medical Center, 1200 E. Broad St., 14th Floor, P.O. Box 980341, Richmond, VA, 23298, USA. hannah.lee@vcuhealth.org.

Joseph Ahn (J)

Division of Gastroenterology and Hepatology, Oregon Health and Science University, Portland, OR, USA.

W Ray Kim (WR)

Division of Gastroenterology and Hepatology, Stanford University, Stanford, CA, USA.

Joseph K Lim (JK)

Yale University, New Haven, CT, USA.

Mindie Nguyen (M)

Division of Gastroenterology and Hepatology, Stanford University, Stanford, CA, USA.

Calvin Q Pan (CQ)

Division of Gastroenterology and Hepatology, NYU Langone Health, NYU School of Medicine, New York, USA.

Donghee Kim (D)

Division of Gastroenterology and Hepatology, Stanford University, Stanford, CA, USA.

Ajitha Mannalithara (A)

Division of Gastroenterology and Hepatology, Stanford University, Stanford, CA, USA.

Helen Te (H)

Digestive Disease Center, University of Chicago, Chicago, IL, USA.

Huy Trinh (H)

San Jose Gastroenterology, San Jose, CA, USA.

Danny Chu (D)

Albert Einstein College of Medicine, New York, NY, USA.

Tram Tran (T)

Department of Medicine, Cedars Sinai Medical Center, Los Angeles, CA, USA.

Jocelyn Woog (J)

Asian Health Foundation, Rochester, MN, USA.

Anna S Lok (AS)

Division of Gastroenterology and Hepatology, University of Michigan, Ann Arbor, MI, USA.

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Classifications MeSH