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57963
registered interest false more like this
date less than 2014-06-04more like thismore than 2014-06-04
answering body
Department of Health more like this
answering dept id 17 more like this
answering dept short name Health more like this
answering dept sort name Health more like this
hansard heading Cystic Fibrosis more like this
house id 1 more like this
legislature
25259
pref label House of Commons more like this
question text To ask the Secretary of State for Health, with reference to the Cystic Fibrosis Trust's report entitled Hope for More: Improving access to lung transplantation and care for people with cystic fibrosis, what assessment he has made of the donor lung utilisation rate for transplantation; and what measures he has identified as having the greatest potential to increase such utilisation. more like this
tabling member constituency York Outer more like this
tabling member printed
Julian Sturdy remove filter
uin 199027 more like this
answer
answer
is ministerial correction false more like this
date of answer remove maximum value filtermore like thismore than 2014-06-11
answer text <p>Currently donated lungs are allocated to the designated cardiothoracic transplant centres on a zonal basis. However, the Cardiothoracic Organs Advisory Group (CTAG) have recently reviewed the allocation policy and have recommended that the size of the allocation zones be adjusted to help ensure equity of access. NHS Blood and Transplant (NHSBT) have therefore confirmed that for cardiothoracic organs, the zones will be reviewed in August 2014 to coincide with changes in liver allocation zones and from August 2015, heart and lung zones will be disaggregated and the zones reviewed separately.</p><p> </p><p>CTAG have also recommended that NHSBT reviews the consequences of introducing two levels of priority for listing for lung transplants - urgent and routine, and suggest a national allocation scheme for urgent listed patients, and zonal allocation for routine listed patients.</p><p> </p><p>Any proposed change would need to be validated by NHSBT, who will review the criteria for urgent listing and the statistical modelling of the potential impact of such a system. NHSBT will continue to work closely with the Cystic Fibrosis Trust to improve outcomes for patients requiring lung transplants.</p><p> </p>
answering member constituency Battersea remove filter
answering member printed Jane Ellison more like this
question first answered
less than 2014-06-11T15:43:54.7503328Zmore like thismore than 2014-06-11T15:43:54.7503328Z
answering member
3918
label Biography information for Jane Ellison more like this
tabling member
4079
label Biography information for Julian Sturdy remove filter
49470
registered interest false more like this
date less than 2014-05-01more like thismore than 2014-05-01
answering body
Department of Health more like this
answering dept id 17 more like this
answering dept short name Health more like this
answering dept sort name Health more like this
house id 1 more like this
legislature
25259
pref label House of Commons more like this
question text To ask the Secretary of State for Health, what recent steps he has taken to raise awareness of the conditions that can lead to young sudden cardiac death and sudden death syndrome. more like this
tabling member constituency York Outer more like this
tabling member printed
Julian Sturdy remove filter
uin 197438 more like this
answer
answer
is ministerial correction false more like this
date of answer less than 2014-05-12more like thismore than 2014-05-12
answer text <p>The UK National Screening Committee advises Ministers and the National Health Service in all four countries about all aspects of screening policy and supports implementation. It is currently reviewing the evidence for screening young people between the ages of 12 to 39 years for the major causes of sudden cardiac death. A public consultation will open shortly.</p><p><strong> </strong></p><p>NHS England is working with the Chief Coroner to discuss what the coronial system can do to help reduce sudden cardiac death in the young. As a result, the Chief Coroner has written to local Coroners asking them to make families of those who have died of the condition aware that it may be inherited, and encouraging them to contact either the British Heart Foundation, Cardiac Risk in the Young, or their general practitioner for testing and counselling.</p><p> </p> more like this
answering member constituency Battersea remove filter
answering member printed Jane Ellison more like this
question first answered
less than 2014-05-12T12:00:00.00Zmore like thismore than 2014-05-12T12:00:00.00Z
answering member
3918
label Biography information for Jane Ellison more like this
tabling member
4079
label Biography information for Julian Sturdy remove filter