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Me first
Kate Martin
Join the
#CYPMefirst conversation
Kate @_common_room
Joanna @jo_ _reid
#CYPMefirst
mefirst.org.uk
We have worked in partnership with children, young people and
healthcare staff to develop
• The Me first communication model
• A one day masterclass
• A website, short films and online resources
Me first aims to improve communication
between children, young people and
healthcare staff
#CYPMefirst
mefirst.org.uk
Me first is not about basic
communication skills or
how to ‘talk to a child’
It is about how to
• put CYP at the centre of conversations about their healthcare
• involve them in choices and decisions
• build on the existing skills of healthcare professionals
• focus on the small, practical changes that can make a big
difference
• learn from what works
Use a step by step,
structured framework of
how to speak to young
patients… but not like a
robot. (CYP)
#CYPMefirst
mefirst.org.uk
Communicating with CYP in healthcare:
what are the key issues and challenges?
I should be the one involved in
decisions about my health because I’m
the one feeling the pain, no one else,
no one else knows what I’m feeling, not
them.
CYP
43% CYP said they were not
involved in choices or decisions
about their care
Care Quality
Commission, 2014
#CYPMefirst
mefirst.org.uk
CYP say:
• That communication is often between healthcare staff
and parents.
• That communication with CYP is often limited to
‘social talk’ and non-health related issues.
• They are less involved in making choices and
decisions, or discussions about treatment.
• They are not asked how things should happen.
What impact does this have?
Poor communication and/or lack of involvement in choices
and decisions can:
• Make CYP feel anxious and out of control.
• Cause CYP to be resistant.
• “Make you feel like a condition, not a person”
• Make CYP feel excluded: “You sort of feel left out. I feel
like my parents are the ones with the condition, not me.”
• Cause conflict
Conflict in paediatric healthcare:
The three most common causes were ‘communication
breakdown’, ‘disagreements about treatment’ and
‘unrealistic expectations’. Significant time was taken
up by these conflicts; most often staff nurses,
consultants, doctors in training and matrons.
Forbat et al., 2015
#CYPMefirst
mefirst.org.uk
Website and resources
www.mefirst.org.uk
• Freely accessible
• All our tips are available on line
• Short films showing model in practice
• Everything can be downloaded
• Shared resources that you can apply to
your area
• Upload your own resources and ideas
• Please tweet #CYPMefirst
#CYPMefirst
mefirst.org.uk
Picture of top tips section of the website??
#CYPMefirst
mefirst.org.uk
The resource hub
INCLUDE IMAGE OF THE Me first MODEL HERO PIECE
How do I know that you are
going to listen to me?
Show me that you want to listen to me
• Introduce yourself to me first
#Hellomynameis
• Give me an overview of the key steps of
the conversation.
• If my parents are with me
• Let me know that you want to hear from me
first and then my parents so we all know
that we will be heard
• Check whether I want to speak to you
alone
Some don’t even say ‘hello,
my name is… how are you?’.
It’s hard to talk to them about
sensitive things as it is, especially
if they don’t even introduce
themselves. (CYP)
.
Why am I here?
Help us all (you, me and my parents) to get a shared
understanding of why I am here, my goals, and what the
problem is
• Find out why I think I am here - ask me
first and then my parents.
• Ask me about all of my concerns, about
my life and not just my condition or
symptoms.
• Explain to me why I am seeing you
specifically and what your expertise is.
Sometimes when my mum
takes me to see the Doctor
we have different ideas about
what the problem is and they
always listen to her. (CYP)
What are my choices?
Ensure I understand the choices available to me and their pros
and cons
• Ask me about what I think could help.
• Remember there are always choices
Options about what can happen
Options about how things can happen
• Talk with me about the pros and cons
of my different options.
The difficult thing is because in
most cases the CYP requires some
treatment, so I tend to be firm and say
“We have got to do something (…) now
we could try this or we could do that.
What do you think?” (Hannah,
Occupational Therapist)
How do you know
what is important to me?
Explore my views and preferences
• Ask me what I think would work best
for me and my life.
• Ask me if there is anything I’m
worried or unsure about.
• Find out my hopes, aims and goals
as these will influence my choices.
• Discuss whether my choices will help
me to achieve these goals.
This is their disease, they
have lived with this, they know
more about it than I do sometimes.
By understanding that, it helps us
make shared decisions.
(Amy, Practice Educator)
What decision have
we made?
Help us all to reach a shared
agreement on what is going
to happen next
• Check that we all agree on
what is going to happen.
• Check that we all agree on
how it will happen.
I like to say “We can always
go back to other options if this does
not work for you. It’s OK to change”.
It helps alleviate the pressure of
agreeing to a treatment plan.
(Faraday, Physiotherapist)
What will happen
next?
Summarise the conversation,
check our understanding, and
help me to rememberSummarise and check
• That we have covered everything
• If I have any questions
• That I know what I need to do and
look out for
• That I am clear about what to
expect next, what to do if
something differs from the agreed
plan and how any changes will be
communicated with me
• What will help me to remember this
At the end of the conversation
you just want them to repeat and
say ‘you’ve got this, you need to do
this, this and this to sort it.’ One clear
cut way, so you remember everything
and to make some notes to take
away.” (CYP)
At the end of each appointment,
I ask a young person and parent
separately to rate out of 10 how helpful the
appointment was. And if it was say, 6/10, I
would ask “Let’s think about what would
make it 7 out of 10 for you today.”
(Anna, Nurse Consultant)
#CYPMefirst
mefirst.org.uk
The impact of the Masterclass on
communication skills with young people
We have now trained over 200 healthcare professionals .
Me first has been independently evaluated by the Evidenced Based Practice Unit (UCL and Anna
Freud Centre).
Three survey’s: Pre training, at the end of the session, and 6-8 weeks post-training.
Me first significantly improves each the attitudes and communications skills of attendee’s and this i
ncrease is sustained at time point 3, 6-8 weeks post training.
- Action –orientated listening
- Exploratory listening
- Consensus orientated listening
- Receptive listening

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Improving Communication Between Healthcare Staff and Young Patients

  • 2. Join the #CYPMefirst conversation Kate @_common_room Joanna @jo_ _reid
  • 3. #CYPMefirst mefirst.org.uk We have worked in partnership with children, young people and healthcare staff to develop • The Me first communication model • A one day masterclass • A website, short films and online resources Me first aims to improve communication between children, young people and healthcare staff
  • 4. #CYPMefirst mefirst.org.uk Me first is not about basic communication skills or how to ‘talk to a child’ It is about how to • put CYP at the centre of conversations about their healthcare • involve them in choices and decisions • build on the existing skills of healthcare professionals • focus on the small, practical changes that can make a big difference • learn from what works Use a step by step, structured framework of how to speak to young patients… but not like a robot. (CYP)
  • 5. #CYPMefirst mefirst.org.uk Communicating with CYP in healthcare: what are the key issues and challenges?
  • 6. I should be the one involved in decisions about my health because I’m the one feeling the pain, no one else, no one else knows what I’m feeling, not them. CYP
  • 7. 43% CYP said they were not involved in choices or decisions about their care Care Quality Commission, 2014
  • 8. #CYPMefirst mefirst.org.uk CYP say: • That communication is often between healthcare staff and parents. • That communication with CYP is often limited to ‘social talk’ and non-health related issues. • They are less involved in making choices and decisions, or discussions about treatment. • They are not asked how things should happen.
  • 9. What impact does this have? Poor communication and/or lack of involvement in choices and decisions can: • Make CYP feel anxious and out of control. • Cause CYP to be resistant. • “Make you feel like a condition, not a person” • Make CYP feel excluded: “You sort of feel left out. I feel like my parents are the ones with the condition, not me.” • Cause conflict
  • 10. Conflict in paediatric healthcare: The three most common causes were ‘communication breakdown’, ‘disagreements about treatment’ and ‘unrealistic expectations’. Significant time was taken up by these conflicts; most often staff nurses, consultants, doctors in training and matrons. Forbat et al., 2015
  • 11. #CYPMefirst mefirst.org.uk Website and resources www.mefirst.org.uk • Freely accessible • All our tips are available on line • Short films showing model in practice • Everything can be downloaded • Shared resources that you can apply to your area • Upload your own resources and ideas • Please tweet #CYPMefirst
  • 12. #CYPMefirst mefirst.org.uk Picture of top tips section of the website??
  • 14. INCLUDE IMAGE OF THE Me first MODEL HERO PIECE
  • 15. How do I know that you are going to listen to me? Show me that you want to listen to me • Introduce yourself to me first #Hellomynameis • Give me an overview of the key steps of the conversation. • If my parents are with me • Let me know that you want to hear from me first and then my parents so we all know that we will be heard • Check whether I want to speak to you alone Some don’t even say ‘hello, my name is… how are you?’. It’s hard to talk to them about sensitive things as it is, especially if they don’t even introduce themselves. (CYP) .
  • 16. Why am I here? Help us all (you, me and my parents) to get a shared understanding of why I am here, my goals, and what the problem is • Find out why I think I am here - ask me first and then my parents. • Ask me about all of my concerns, about my life and not just my condition or symptoms. • Explain to me why I am seeing you specifically and what your expertise is. Sometimes when my mum takes me to see the Doctor we have different ideas about what the problem is and they always listen to her. (CYP)
  • 17. What are my choices? Ensure I understand the choices available to me and their pros and cons • Ask me about what I think could help. • Remember there are always choices Options about what can happen Options about how things can happen • Talk with me about the pros and cons of my different options. The difficult thing is because in most cases the CYP requires some treatment, so I tend to be firm and say “We have got to do something (…) now we could try this or we could do that. What do you think?” (Hannah, Occupational Therapist)
  • 18. How do you know what is important to me? Explore my views and preferences • Ask me what I think would work best for me and my life. • Ask me if there is anything I’m worried or unsure about. • Find out my hopes, aims and goals as these will influence my choices. • Discuss whether my choices will help me to achieve these goals. This is their disease, they have lived with this, they know more about it than I do sometimes. By understanding that, it helps us make shared decisions. (Amy, Practice Educator)
  • 19. What decision have we made? Help us all to reach a shared agreement on what is going to happen next • Check that we all agree on what is going to happen. • Check that we all agree on how it will happen. I like to say “We can always go back to other options if this does not work for you. It’s OK to change”. It helps alleviate the pressure of agreeing to a treatment plan. (Faraday, Physiotherapist)
  • 20. What will happen next? Summarise the conversation, check our understanding, and help me to rememberSummarise and check • That we have covered everything • If I have any questions • That I know what I need to do and look out for • That I am clear about what to expect next, what to do if something differs from the agreed plan and how any changes will be communicated with me • What will help me to remember this At the end of the conversation you just want them to repeat and say ‘you’ve got this, you need to do this, this and this to sort it.’ One clear cut way, so you remember everything and to make some notes to take away.” (CYP) At the end of each appointment, I ask a young person and parent separately to rate out of 10 how helpful the appointment was. And if it was say, 6/10, I would ask “Let’s think about what would make it 7 out of 10 for you today.” (Anna, Nurse Consultant)
  • 21. #CYPMefirst mefirst.org.uk The impact of the Masterclass on communication skills with young people We have now trained over 200 healthcare professionals . Me first has been independently evaluated by the Evidenced Based Practice Unit (UCL and Anna Freud Centre). Three survey’s: Pre training, at the end of the session, and 6-8 weeks post-training. Me first significantly improves each the attitudes and communications skills of attendee’s and this i ncrease is sustained at time point 3, 6-8 weeks post training. - Action –orientated listening - Exploratory listening - Consensus orientated listening - Receptive listening