Mortality rates among patients successfully treated for hepatitis C in the era of interferon-free antivirals: population based cohort study

被引:25
作者
Hamill, Victoria [1 ,2 ]
Wong, Stanley [3 ]
Benselin, Jennifer [4 ,5 ,6 ]
Krajden, Mel [3 ,7 ]
Hayes, Peter C. [8 ]
Mutimer, David [9 ]
Yu, Amanda [3 ]
Dillon, John F. [10 ]
Gelson, William [11 ]
Garcia, Hector A. Velasquez [3 ,12 ]
Yeung, Alan [1 ,2 ]
Johnson, Philip [13 ]
Barclay, Stephen [14 ]
Alvarez, Maria [3 ]
Toyoda, Hidenori [15 ]
Agarwal, Kosh [16 ]
Fraser, Andrew [17 ,18 ]
Bartlett, Sofia [3 ,7 ]
Aldersley, Mark [19 ]
Bathgate, Andy [8 ]
Binka, Mawuena [3 ]
Richardson, Paul [20 ]
Morling, Joanne R. [4 ,5 ,6 ,21 ]
Ryder, Stephen [4 ,5 ]
MacDonald, Douglas [22 ]
Hutchinson, Sharon
Barnes, Eleanor [23 ,24 ]
Guha, Indra Neil [4 ,5 ,6 ]
Irving, William L. [4 ,5 ,6 ]
Janjua, Naveed Z. [3 ,12 ,25 ]
Innes, Hamish [1 ,2 ,21 ]
机构
[1] Glasgow Caledonian Univ, Sch Hlth & Life Sci, Glasgow, Scotland
[2] Publ Hlth Scotland, Glasgow, Scotland
[3] British Columbia Ctr Dis Control, Vancouver, BC, Canada
[4] Nottingham Univ Hosp NHS Trust, NIHR Nottingham Biomed Res Ctr, Nottingham, England
[5] Univ Nottingham, Nottingham, England
[6] Univ Nottingham, Nottingham Digest Dis Ctr, Sch Med, Nottingham, England
[7] Univ British Columbia, Dept Pathol & Lab Med, Vancouver, BC, Canada
[8] Royal Infirm Edinburgh NHS Trust, Edinburgh, Scotland
[9] Univ Hosp Birmingham NHS Fdn Trust, Queen Elizabeth Hosp, Liver & Hepatol Unit, Birmingham, England
[10] Univ Dundee, Sch Med, Div Mol & Clin Med, Dundee, Scotland
[11] Cambridge Univ Hosp NHS Fdn Trust, Cambridge Liver Unit, Cambridge, England
[12] Univ British Columbia, Sch Populat & Publ Hlth, Vancouver, BC, Canada
[13] Univ Liverpool, Dept Mol & Clin Canc Med, Liverpool, England
[14] Glasgow Royal Infirm, Glasgow, Scotland
[15] Ogaki Municipal Hosp, Dept Gastroenterol, Ogaki, Japan
[16] Kings Coll Hosp NHS Fdn Trust, Inst Liver Studies, London, England
[17] Aberdeen Royal Infirm, Aberdeen, Scotland
[18] Queen Elizabeth Univ Hosp, Glasgow, Scotland
[19] St James Univ Hosp, Leeds Liver Unit, Leeds, England
[20] Royal Liverpool & Broadgreen Univ Hosp NHS Trust, Liverpool, England
[21] Univ Nottingham, Lifespan & Populat Hlth, Nottingham, England
[22] Royal Free London NHS Fdn Trust, Gastroenterol & Hepatol, London, England
[23] Univ Oxford, Nuffield Dept Med, Oxford, England
[24] Univ Oxford, Oxford NIHR Biomed Res Ctr, Oxford, England
[25] St Pauls Hosp, Ctr Hlth Evaluat & Outcome Sci, Vancouver, BC, Canada
来源
BMJ-BRITISH MEDICAL JOURNAL | 2023年 / 382卷
关键词
SUSTAINED VIROLOGICAL RESPONSE; CHRONIC HCV INFECTION; THERAPY; CIRRHOSIS; IMPACT;
D O I
10.1136/bmj-2022-074001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVES To quantify mortality rates for patients successfully treated for hepatitis C in the era of interferon-free, direct acting antivirals and compare these rates with those of the general population.DESIGN Population based cohort study.SETTING British Columbia, Scotland, and England (England cohort consists of patients with cirrhosis only).PARTICIPANTS 21 790 people who were successfully treated for hepatitis C in the era of interferon-free antivirals (2014-19). Participants were divided into three liver disease severity groups: people without cirrhosis (pre-cirrhosis), those with compensated cirrhosis, and those with end stage liver disease. Follow-up started 12 weeks after antiviral treatment completion and ended on date of death or 31 December 2019.MAIN OUTCOME MEASURES Crude and age-sex standardised mortality rates, and standardised mortality ratio comparing the number of deaths with that of the general population, adjusting for age, sex, and year. Poisson regression was used to identify factors associated with all cause mortality rates.RESULTS 1572 (7%) participants died during follow-up. The leading causes of death were drug related mortality (n=383, 24%), liver failure (n=286, 18%), and liver cancer (n=250, 16%). Crude all cause mortality rates (deaths per 1000 person years) were 31.4 (95% confidence interval 29.3 to 33.7), 22.7 (20.7 to 25.0), and 39.6 (35.4 to 44.3) for cohorts from British Columbia, Scotland, and England, respectively. All cause mortality was considerably higher than the rate for the general population across all disease severity groups and settings; for example, all cause mortality was three times higher among people without cirrhosis in British Columbia (standardised mortality ratio 2.96, 95% confidence interval 2.71 to 3.23; P<0.001) and more than 10 times higher for patients with end stage liver disease in British Columbia (13.61, 11.94 to 15.49; P<0.001). In regression analyses, older age, recent substance misuse, alcohol misuse, and comorbidities were associated with higher mortality rates.CONCLUSION Mortality rates among people successfully treated for hepatitis C in the era of interferon-free, direct acting antivirals are high compared with the general population. Drug and liver related causes of death were the main drivers of excess mortality. These findings highlight the need for continued support and follow-up after successful treatment for hepatitis C to maximise the impact of direct acting antivirals.
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