New survey launches to identify alcohol-related liver disease research uncertainties
- 22 June 2015
- 4 min read
Today, the NIHR and the British Society of Gastroenterology (BSG) have opened a survey to collect important information to help prioritise unanswered questions about alcohol-related liver disease (ARLD).
The survey gives patients, carers, clinicians and family members affected by the disease an opportunity to have their say and influence future research in the area.
The liver is the main organ that processes alcohol, so heavy drinking over a period of years can lead to potentially life-threatening conditions. Alcohol-related liver disease encompasses a range of liver damage from simple fatty liver, through to fibrosis, cirrhosis, portal hypertension and chronic liver failure, frequently accompanied by sudden episodes of acute or chronic cholestatic liver failure (termed alcoholic hepatitis).
Between 1987 and 2001, UK deaths caused by liver cirrhosis (largely caused by alcohol) increased, as did alcohol consumption levels. Cirrhosis deaths more than doubled over the same period in Scotland alone and are now among the highest in Western Europe.
Alcoholic liver disease has become the most common type of alcohol-related death in England. It accounted for 64 percent (4,441) of all alcohol-related deaths in 2011, and for 65 percent and 62 percent of male and female alcohol-related deaths respectively - most among those aged 50-59 years.
Set up through a James Lind Alliance (JLA) Priority Setting Partnership (PSP), the project is guided by a steering group and supported by a number of organisations including The British Liver Trust and Alcohol Health Alliance UK. JLA PSPs are about ‘tackling treatment uncertainties together’. Patient/carer organisations and clinician organisations work together to confront uncertainties surrounding the effects of treatments in their area of interest.
The project encourages those who have unanswered questions around the diagnosis, prevention, care or treatment of alcohol-related liver disease to get involved by completing the survey. Some of the ways that you can help make the project a success include: completing the survey; passing on the information to encourage family members, support networks, carers or colleagues to fill in the survey; and circulating copies of the PSP postcard to relevant groups.
The results of the survey will be published in 2016 and will include a ‘top ten’ list of priorities for clinical research, as determined by those people affected.
Please get involved and help put ARLD research in the spotlight.
Please contact us if you have any questions.