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Enhanced Patient Care –  Exploiting the Social Web Environments   10th EFAS Congress, 22 – 25 June, 2011 Warsaw, Poland   Dr. Dr. h.c. Monika Lehnhardt
Enhanced Patient Care – why is it desirable or even inevitable?   ,[object Object],[object Object],[object Object],[object Object],[object Object]
Web 2.0 Social Web:  How mass collaboration changes everything   ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Communication in Social Web Environments  in various structures   ,[object Object],[object Object],[object Object]
Social Web “en route”  from Neonatal Hearing Screening to Early Intervention and Long-Term Care Access Internet  search for information contact experts, clinics, CI centers, manufacturers of HAs and CIs   Confronted with an overwhelming amount of information Access Web 2.0 Social Media; Contact parents, exchange knowledge, Cooperate Return to experts – shared decision-making ‘participative medicine’ Talk to parents of babies/children with CI; Contact surgeons, audiologists, therapists on a GLOBAL BASIS;  NHS  parents’ suspicion pass or fail  confirmation  shock, denial, confusion, anger, sadness, desperation  action (search for information - limited results)  present child for in-depth diagnosis hearing problem/deafness confirmed  action (search for information - limited results) small ‘objective’ basis to make a decision  decision which therapy is the most suitable for the child and the family   1 st  phase of (re)habilitation provision of HA decision for or against CI (based on limited and ‘local’ knowledge) 
Social Web “en route”  from Neonatal Hearing Screening to Early Intervention and Long-Term Care Talk to the surgeon also in his ‘consulting hours’ YouTube “Cochlear Implant Activation” 524 results; Keep contact with professionals AND parents (weblogs, SKYPE, chat-rooms, conference rooms) remote fitting and counseling;   remote support CI recipients contact each other – Network – regardless of age   CI surgery (surgeon has limited time for consultation)  First fitting (unsure what to expect)    repeated fitting sessions and (re)habilitation, counseling of parents   (limited by ease of access, time constraints)  Annual medical check-up at the implant clinic;  occasional fitting and counseling;  The teenager CI recipient may need support to successfully attend mainstream schools and institutions for higher education (maybe not easily available, expensive)   Inclusion
Illustration of using the Social Web Environment for a family whose child has been diagnosed as deaf
 
Examples of already existing communities focusing on Cochlear Implants ,[object Object],[object Object],[object Object],[object Object],[object Object]
Call for Action ,[object Object]

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Dr. Dr. h.c. Monika Lehnhardt - Enhanced Patient Care - Exploiting the Social Web Environments

  • 1. Enhanced Patient Care – Exploiting the Social Web Environments 10th EFAS Congress, 22 – 25 June, 2011 Warsaw, Poland Dr. Dr. h.c. Monika Lehnhardt
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  • 5. Social Web “en route” from Neonatal Hearing Screening to Early Intervention and Long-Term Care Access Internet search for information contact experts, clinics, CI centers, manufacturers of HAs and CIs   Confronted with an overwhelming amount of information Access Web 2.0 Social Media; Contact parents, exchange knowledge, Cooperate Return to experts – shared decision-making ‘participative medicine’ Talk to parents of babies/children with CI; Contact surgeons, audiologists, therapists on a GLOBAL BASIS; NHS parents’ suspicion pass or fail confirmation  shock, denial, confusion, anger, sadness, desperation  action (search for information - limited results)  present child for in-depth diagnosis hearing problem/deafness confirmed  action (search for information - limited results) small ‘objective’ basis to make a decision  decision which therapy is the most suitable for the child and the family  1 st phase of (re)habilitation provision of HA decision for or against CI (based on limited and ‘local’ knowledge) 
  • 6. Social Web “en route” from Neonatal Hearing Screening to Early Intervention and Long-Term Care Talk to the surgeon also in his ‘consulting hours’ YouTube “Cochlear Implant Activation” 524 results; Keep contact with professionals AND parents (weblogs, SKYPE, chat-rooms, conference rooms) remote fitting and counseling; remote support CI recipients contact each other – Network – regardless of age CI surgery (surgeon has limited time for consultation)  First fitting (unsure what to expect)  repeated fitting sessions and (re)habilitation, counseling of parents (limited by ease of access, time constraints)  Annual medical check-up at the implant clinic; occasional fitting and counseling;  The teenager CI recipient may need support to successfully attend mainstream schools and institutions for higher education (maybe not easily available, expensive)  Inclusion
  • 7. Illustration of using the Social Web Environment for a family whose child has been diagnosed as deaf
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