| Literature DB >> 27933202 |
Yoona A Kim1, Jacqueline Estevez1, An Le1, Dennis Israelski2, Oidov Baatarkhuu3, Tserenchimed Sarantuya4, Sonom Narantsetseg5, Pagbajabyn Nymadawa6, Richard H Le1, Man-Fung Yuen7, Geoffrey Dusheiko8, Mario Rizzetto9, Mindie H Nguyen10.
Abstract
BACKGROUND: According to Globocan, Mongolia has the highest worldwide hepatocellular carcinoma (HCC) incidence (78.1/100 000, 3.5× higher than China). AIMS AND METHODS: We conducted an anonymous survey of physicians from major provinces who attended an educational liver symposium, analysing their demography, practice, knowledge, perceptions and proposed solutions. Multivariate logistic regression was used to estimate OR relating demography and practice factors with higher provider knowledge and improvement.Entities:
Keywords: CHRONIC VIRAL HEPATITIS; HEPATITIS B; HEPATOCELLULAR CARCINOMA
Year: 2016 PMID: 27933202 PMCID: PMC5128837 DOI: 10.1136/bmjgast-2016-000119
Source DB: PubMed Journal: BMJ Open Gastroenterol ISSN: 2054-4774
Baseline demographics of the physician attendees
| N (%) | |
|---|---|
| Gender (n=107) | |
| Male | 14 (13.1) |
| Female | 93 (86.9) |
| Age range (n=107) (years) | |
| 20–30 | 11 (10.3) |
| 31–40 | 29 (27.1) |
| 41–50 | 44 (41.1) |
| 51–60 | 19 (17.8) |
| 61–70 | 4 (3.7) |
| ≥71 | 0 (0) |
| Years of practice (n=106) | |
| 0–10 | 30 (28.3) |
| 11–20 | 30 (28.3) |
| 21–25 | 19 (17.9) |
| 26–35 | 23 (21.7) |
| ≥36 | 4 (3.8) |
| Specialty (n=106) | |
| Family medicine | 0 (0) |
| Internal medicine | 19 (17.9) |
| Gastroenterology | 34 (32.1) |
| Hepatology | 8 (7.6) |
| Infectious disease | 38 (35.9) |
| Paediatrics | 1 (0.9) |
| Primary medicine practice (n=102) | |
| Referral government hospital | 28 (27.5) |
| General government hospital | 53 (52.0) |
| Referral private hospital | 3 (2.9) |
| General private hospital | 12 (11.8) |
| General primary care public clinic | 5 (4.9) |
| University affiliation (n=100) | |
| Yes—university on campus/trainees involved | 29 (29.0) |
| Yes—university unattached/trainees not involved | 44 (44.0) |
| Not affiliated | 26 (26.0) |
Characteristics of physician practices
| N (%) | |
|---|---|
| Size of facility (n=102) | |
| ≥500 bed hospital | 12 (11.8) |
| 300–500 bed hospital | 16 (15.7) |
| 100–300 bed hospital | 34 (33.3) |
| ≤100 bed hospital | 9 (8.8) |
| 2–5 physician clinics | 6 (5.9) |
| ≥11 physician clinics | 3 (2.9) |
| Location of practice (n=103) | |
| Rural | 40 (38.8) |
| Urban | 63 (61.2) |
| Patients with liver disease seen per week (n=105) | |
| <10 | 23 (21.9) |
| 11–30 | 41 (39.1) |
| 31–50 | 17 (16.2) |
| 51–75 | 6 (5.7) |
| 76–100 | 6 (5.7) |
| 101–150 | 7 (6.7) |
| >150 | 5 (4.8) |
| Percentage of patients with liver disease with HCV (n=105) | |
| <10 | 20 (19.1) |
| 11–25 | 43 (41.0) |
| 26–50 | 33 (31.4) |
| 51–75 | 9 (8.6) |
| 76–100 | 0 (0) |
| Percentage of patients with liver disease with HBV (n=104) | |
| <10 | 23 (22.1) |
| 11–25 | 46 (44.2) |
| 26–50 | 28 (26.9) |
| 51–75 | 6 (5.8) |
| 76–100 | 1 (1.0) |
| Percentage of patients with liver disease with HDV/HBV coinfection (n=103) | |
| <10 | 67 (65.1) |
| 11–25 | 27 (26.2) |
| 26–50 | 7 (6.8) |
| 51–75 | 2 (1.9) |
| 76–100 | 0 (0) |
| Percentage of patients with liver disease with compensated cirrhosis (n=103) | |
| <10 | 36 (35.0) |
| 11–25 | 35 (34.0) |
| 26–50 | 27 (26.2) |
| 51–75 | 5 (4.9) |
| 76–100 | 0 (0) |
| Percentage of patients with liver disease with decompensated cirrhosis (n=103) | |
| <10 | 49 (47.6) |
| 11–25 | 22 (21.4) |
| 26–50 | 23 (22.3) |
| 51–75 | 5 (4.9) |
| 76–100 | 4 (3.9) |
| Percentage of patients with liver disease with HCC (n=101) | |
| <10 | 77 (76.2) |
| 11–25 | 18 (17.8) |
| 26–50 | 3 (3.0) |
| 51–75 | 3 (3.0) |
| 76–100 | 0 (0) |
HBV, hepatitis B virus; HCC, hepatocellular carcinoma; HCV, hepatitis C virus; HDV, hepatitis D virus.
Physician perceived barriers of hepatitis and hepatocellular carcinoma screening
| Perceived barriers to screening | Hepatitis B (%) | Hepatitis C (%) | Hepatitis D (%) | Hepatocellular carcinoma (%) |
|---|---|---|---|---|
| Asymptomatic disease | 10.5 | 18.6 | 9.4 | 8.2 |
| Poor patient awareness and education | 13.2 | 21.4 | 11.5 | 20.6 |
| Provider's lack of time and resources | 9.2 | 10.0 | 2.1 | 2.7 |
| Lack of screening and management guidelines or awareness of guidelines | 15.8 | 11.4 | 24.0 | 17.8 |
| Patients living too far from laboratories and/or clinics | 10.5 | 4.3 | 12.5 | 12.3 |
| Lack of access to hepatitis B treatment | 10.5 | 7.1 | 5.2 | 1.4 |
| Patient's inability to pay for tests | 25.0 | 24.3 | 30.2 | 37.0 |
| Difficulty accessing specialty care | 5.3 | 2.9 | 5.2 | 0 |
Physician perceived barriers of hepatitis B and C treatment
| Perceived barriers to treatment | Hepatitis B (%) | Hepatitis C (%) |
|---|---|---|
| Cost of medication | 14.9 | 25.3 |
| Cost of blood test, medical visits, in addition to cost of medication | 10.3 | 8.4 |
| Active substance abuse | 1.2 | 2.1 |
| Active psychiatric comorbidity | 0 | 0 |
| Patient's fear of side effects | 0 | 0 |
| Lack of consensus about screening and treatment guidelines | 5.8 | 10.5 |
| Lack of provider education about treatment and side effect management | 2.3 | 0 |
| Distance to treating physicians | 0 | 1.1 |
| More than 3 of above | 65.5 | 52.6 |
Physician survey results on priorities for screening and treatment for CHB
| Priorities for screening and management | n (%) |
|---|---|
| Which patients do you think should be screened for hepatitis B infection? (n=64) | |
| High-risk populations (pregnant women, persons with multiple sex partners, inmates, etc) | 32 (50.0) |
| Older patients (>55 years) | 1 (1.6) |
| All patients | 31 (48.4) |
| Which patients with hepatitis B should be prioritised for treatment? (n=74) | |
| All patients with compensated or decompensated cirrhosis, regardless of ALT levels, HBeAg status or HBV DNA levels | 33 (44.6) |
| Only patients with decompensated cirrhosis, regardless of ALT levels, HBeAg status or HBV DNA levels | 12 (16.2) |
| Adults with CHB who do not have clinical evidence of cirrhosis, but are older and have highly persistently abnormal ALT levels and evidence of high-level HBV replication, regardless of HBeAg status | 24 (32.4) |
| Patients with persistently abnormal ALT levels alone, regardless of HBeAg status (where HBV DNA testing is not available) | 5 (6.8) |
| Which patients need to be screened for HDV coinfection? (n=86) | |
| Patients known to be HBsAg positive and symptomatic | 37 (43.0) |
| All patients known to be HBsAg positive, including asymptomatic patients | 40 (46.5) |
| Patients with acute hepatitis B who are not yet HBsAg positive, but are IgM anti-HBc positive | 4 (4.7) |
| Chronic HBV carriers with a history of or active injection drug use | 4 (4.7) |
| No patients should be screened | 1 (1.2) |
ALT, alanine aminotransferase; anti-HBc, hepatitis B core antibody; CHB, chronic hepatitis B; HBeAg, hepatitis B envelope antigen; HBsAg, hepatitis B surface antigen; HBV, hepatitis B virus; HDV, hepatitis D virus.
Physician survey results on priorities for screening and treatment for chronic hepatitis C
| Priorities for screening and management | n (%) |
|---|---|
| Which patients need to be screened for HCV infection? (n=91) | |
| A. History of or current injection drug use | 3 (3.3) |
| B. Healthcare workers | 1 (1.1) |
| C. Children born to HCV-infected women | 0 (0) |
| D. Prior recipients of medical procedures, such as transfusions, organ transplants, haemodialysis, surgical procedures | 4 (4.4) |
| E. Patients with unexplained ALT levels | 2 (2.2) |
| F. All patients with A–E | 65 (71.4) |
| G. All older patients | 16 (17.6) |
| Which patients should be prioritised for HCV treatment? (n=81) | |
| A. Patients with advanced fibrosis or cirrhosis (stages 3–4) | 11 (13.6) |
| B. Patients with cirrhosis | 1 (1.2) |
| C. Liver transplant recipients or patients on immunosuppression for other diseases | 1 (1.2) |
| D. Patients with severe extrahepatic hepatitis C | 3 (3.7) |
| E. Patients with HIV coinfection | 2 (2.5) |
| F. Patients with HBV coinfection | 0 (0) |
| G. Patients with other coexistent liver diseases (eg, NASH) | 29 (35.8) |
| H. All patients A–G | 22 (27.2) |
| I. All patients with chronic HCV regardless of severity | 12 (14.8) |
ALT, alanine aminotransferase; HBV, hepatitis B virus; HCV, hepatitis C virus; NASH, nonalcoholic steatohepatitis.
Figure 1Mean ratings for proposal of future educational programmes to improve provider knowledge (1 as ‘least useful’ to 5 as ‘most useful’). CME, Continuing Medical Education.
Figure 2Mean ratings for proposal of future efforts to improve screening (1 as ‘least useful’ to 5 as ‘most useful’).