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OSA
                 The patient’s perspective
                   and 3rd sector view
                    National Respiratory Learning Event
                            21st February 2013
                      Judy Harris and Lucy Bramwell




    About the BLF
    The BLF is the UK’s lung charity


    •      We offer support to the one in five people in the UK who have a lung
           condition
    •      We promote greater understanding of lung disease
    •      We campaign for positive change
    •      We fund new research




www.blf.org.uk                                                      © British Lung Foundation 2012




                                                                                                     1
The BLF OSA campaign
    Objectives:
           To promote OSA as a regional and national priority in
           England, Scotland, Wales and Northern Ireland, in order to
           improve services along the patient pathway for people with
           OSA


           To help increase awareness of OSA to the general public and
           health care professionals, especially primary care, to find
           undiagnosed people and improve their quality of life




www.blf.org.uk                                                      © British Lung Foundation 2012




    The OSA Charter
    •      Campaign tool
    •      3 parts:


     Rights of people with OSA
     Calls to Governments across UK
     Encouraging employers




www.blf.org.uk                                                      © British Lung Foundation 2012




                                                                                                     2
The patient’s perspective
    Signs and symptoms


    •      Public awareness of OSA (BLF surveys suggest 50% men and 60%
           women have heard of OSA)


    •      Awareness of key symptoms


    •      Support from primary care; BLF GP guide; recognising symptoms –
           day and night; screening; referral




www.blf.org.uk                                                     © British Lung Foundation 2012




    The patient’s perspective
    Referral


    •      Access to local sleep clinic


    •      Joined up working between primary, secondary and tertiary care –
           protocols


    •      Clear pathway at point of referral


    •      Prioritising those most at risk



www.blf.org.uk                                                     © British Lung Foundation 2012




                                                                                                    3
The patient’s perspective
    Assessment and Diagnosis


    •      Sleep services in each region for children and adults


    •      Fast track drivers, patients with co-morbidities (hypertension and
           type 2 diabetes)


    •      Agreed minimum standards




www.blf.org.uk                                                       © British Lung Foundation 2012




    The patient’s perspective
    Treatment


    •      Agreed minimum standards


    •      Access to:
     Continuous Positive Airways Pressure (CPAP) – recommended for
      moderate to severe OSA
     Other treatments – mandibular advancement (MAD), lifestyle
      changes, surgery (tonsillectomy, bariatric, mandibular advancement)
     Education and Information



www.blf.org.uk                                                       © British Lung Foundation 2012




                                                                                                      4
The patient’s perspective
    Management


    •      Patient information and education


    •      On-going clinical support


    •      Patient Voice




www.blf.org.uk                                                         © British Lung Foundation 2012




    Patient voice - adult
    •      My CPAP is like a comfort blanket. After the first night with it, I was
           bouncing off the walls – I had never felt like that before. It was
           brilliant, absolutely brilliant.
    •      A sleep test showed I stopped breathing 54 times an hour during the
           night. With the treatment I am doing really well and feel like a
           completely different person.
    •      I've now been using the mandibular advancement device for just
           over 4 weeks now which is reasonably comfortable to wear. It does
           take some getting used to, but I do get a better quality of sleep -
           and possibly more importantly, so does my wife.




www.blf.org.uk                                                         © British Lung Foundation 2012




                                                                                                        5
Patient voice -
                           child
   As a baby, we noticed pauses in his breathing from about eight weeks
   old. Milo used to cry before bedtime and say: ‘I don’t want to go to
   sleep. It makes me tired.’ He was right, sleeping was exhausting for him.
   I took him to the GP many times and we had several trips to A&E, when
   Milo stopped breathing. But it took us a very long time to find out what
   was wrong.
   Milo had an urgent operation to remove his tonsils and adenoids in June
   2012, just after his fourth birthday. The change has been incredible.
   Milo was sleep deprived and oxygen starved for the first for years of his
   life. I think the problem lies in a lack of awareness among GPs of OSA in
   children.


www.blf.org.uk                                                   © British Lung Foundation 2012




    OSA takeaway
    Your OSA pack contains:


    •      Charter
    •      Patient information leaflet
    •      Triple S awareness poster (sample copy)
    •      Take action flyer
    •      GP OSA Guide – launching today!




www.blf.org.uk                                                   © British Lung Foundation 2012




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Breakout 2.1 OSA The patient’s perspective and 3rd sector view - Judy Harris and Lucy Bramwell

  • 1. OSA The patient’s perspective and 3rd sector view National Respiratory Learning Event 21st February 2013 Judy Harris and Lucy Bramwell About the BLF The BLF is the UK’s lung charity • We offer support to the one in five people in the UK who have a lung condition • We promote greater understanding of lung disease • We campaign for positive change • We fund new research www.blf.org.uk © British Lung Foundation 2012 1
  • 2. The BLF OSA campaign Objectives: To promote OSA as a regional and national priority in England, Scotland, Wales and Northern Ireland, in order to improve services along the patient pathway for people with OSA To help increase awareness of OSA to the general public and health care professionals, especially primary care, to find undiagnosed people and improve their quality of life www.blf.org.uk © British Lung Foundation 2012 The OSA Charter • Campaign tool • 3 parts:  Rights of people with OSA  Calls to Governments across UK  Encouraging employers www.blf.org.uk © British Lung Foundation 2012 2
  • 3. The patient’s perspective Signs and symptoms • Public awareness of OSA (BLF surveys suggest 50% men and 60% women have heard of OSA) • Awareness of key symptoms • Support from primary care; BLF GP guide; recognising symptoms – day and night; screening; referral www.blf.org.uk © British Lung Foundation 2012 The patient’s perspective Referral • Access to local sleep clinic • Joined up working between primary, secondary and tertiary care – protocols • Clear pathway at point of referral • Prioritising those most at risk www.blf.org.uk © British Lung Foundation 2012 3
  • 4. The patient’s perspective Assessment and Diagnosis • Sleep services in each region for children and adults • Fast track drivers, patients with co-morbidities (hypertension and type 2 diabetes) • Agreed minimum standards www.blf.org.uk © British Lung Foundation 2012 The patient’s perspective Treatment • Agreed minimum standards • Access to:  Continuous Positive Airways Pressure (CPAP) – recommended for moderate to severe OSA  Other treatments – mandibular advancement (MAD), lifestyle changes, surgery (tonsillectomy, bariatric, mandibular advancement)  Education and Information www.blf.org.uk © British Lung Foundation 2012 4
  • 5. The patient’s perspective Management • Patient information and education • On-going clinical support • Patient Voice www.blf.org.uk © British Lung Foundation 2012 Patient voice - adult • My CPAP is like a comfort blanket. After the first night with it, I was bouncing off the walls – I had never felt like that before. It was brilliant, absolutely brilliant. • A sleep test showed I stopped breathing 54 times an hour during the night. With the treatment I am doing really well and feel like a completely different person. • I've now been using the mandibular advancement device for just over 4 weeks now which is reasonably comfortable to wear. It does take some getting used to, but I do get a better quality of sleep - and possibly more importantly, so does my wife. www.blf.org.uk © British Lung Foundation 2012 5
  • 6. Patient voice - child As a baby, we noticed pauses in his breathing from about eight weeks old. Milo used to cry before bedtime and say: ‘I don’t want to go to sleep. It makes me tired.’ He was right, sleeping was exhausting for him. I took him to the GP many times and we had several trips to A&E, when Milo stopped breathing. But it took us a very long time to find out what was wrong. Milo had an urgent operation to remove his tonsils and adenoids in June 2012, just after his fourth birthday. The change has been incredible. Milo was sleep deprived and oxygen starved for the first for years of his life. I think the problem lies in a lack of awareness among GPs of OSA in children. www.blf.org.uk © British Lung Foundation 2012 OSA takeaway Your OSA pack contains: • Charter • Patient information leaflet • Triple S awareness poster (sample copy) • Take action flyer • GP OSA Guide – launching today! www.blf.org.uk © British Lung Foundation 2012 6
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