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Redesigning the ED Dr Paul Jarvis Consultant in Emergency Medicine

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  • Redesigning  the  ED  

    Dr  Paul  Jarvis  Consultant  in  Emergency  Medicine  

    The image cannot be displayed. Your computer may not have enough memory to open the image, or the image may have been corrupted. Restart your computer, and then open the file again. If the red x still appears, you may have to delete the image and then insert it again.

  • The results shown here are specific to one health care facility and may differ from those

    achieved by other institutions.

    031778 Rev A 1/14 For In Vitro Diagnostic 2

    Disclaimer

  • Old System

    Tradi;onal  ED  System  

    Treatment

    Disposal Triage

    Dr Review Investigations

    Nurse

    Assessment

    Dr Review Walking

    Ambulance Consultant

    031778 Rev A 1/14 For In Vitro Diagnostic 3

  • What is the problem?

    •  System  designed  to  make  pa;ents  wait    (Triage  is  a  step  to  decide  how  long  you  should  wait)  

    •  Two  access  points  to  the  service    

    •  Inves;ga;ons  requested  late  

    •  Poten;al  for  inexperienced  staff  to  order  unnecessary  inves;ga;ons  

    031778 Rev A 1/14 For In Vitro Diagnostic 4

  • EDIT ED Dr Treatment Disposal

    Ambulance

    Walking

    Consultant Consultant

    EDIT  System  

    Redesign ED Process

    031778 Rev A 1/14 For In Vitro Diagnostic 5

  • •  Introduc;on  of  Point  of  Care  Tes;ng  (POCT)    •     

    •  i-‐STAT®  System    –  CHEM8+  –  CG4+  

    Introduced Point of Care Testing

    31778  Rev A 1/14 For In Vitro Diagnostic i-STAT is a registered trademark of the Abbott Group of Companies in various jurisdictions For Intended Use Information – See Intended Use Section

    6

  • Phase  1  –  Evaluate  the  performance  of  the  tradi;onal  ED  model    -‐    1st  April  to  24th  May  2013  (3835  pa;ents)    

    Phase  2  –  Evaluate  introducing  POCT  into  tradi;onal  ED  model    -‐  28th  May  to  29th  September  2013  (7033  pa;ents)    

    Phase  3  –  Evaluate  POCT  and  EDIT  model  together  –  30th  September  to  18th  October  2013  (1200  pa;ents)  

    3 Phase Trial

    031778 Rev A 1/14 For In Vitro Diagnostic 7

  • Before  Trial      Median  Blood  Results  being  available:  63  minutes  

       Trial  Results      Median:  3  minutes        Able  to  do  60%  of  ED  bloods  using  i-‐STAT  

    Point of Care Testing

    031778 Rev A 1/14 For In Vitro Diagnostic 8

  • Effect of the 3 Different Working Models on the Median ED Times

    68% Overall

    Reduction

    40% Overall

    Reduction

    60% Overall

    Reduction

    Tim

    e hh

    :mm

    Results

    031778 Rev A 1/14 For In Vitro Diagnostic 9

  • Non-EDIT EDIT

    Breach Performance Monday to Friday 9-5

    Consistently meeting 4 hour target Much less variation with EDIT based model

    031778 Rev A 1/14 For In Vitro Diagnostic 10

  • Results

    * - only 1 consultant

    When only 1 consultant causes special cause variation in performance r = -0.8

    UCL

    *

    *

    *Two consultants on duty, except during the days noted 031778 Rev A 1/14 For In Vitro Diagnostic

    11

    Dates 30 Sep – 18 Oct 2013

  •  With  tradi;onal  model  9  pa;ents  are  undergoing  ED  Care  in  the  ED  central  area  at  any  one  ;me  (Monday  to  Friday  9-‐5)    EDIT  &  i-‐STAT  reduces  this  to  5  due  to  quicker  processing  of  pa;ents          

           

    Results

    Reduces Overcrowding

    Frees up time to Care

    031778 Rev A 1/14 For In Vitro Diagnostic 12

  • With  Tradi;onal  Model  3%  of  pa;ents  seen  in  ED  Central  Area  Monday  to  Friday  9-‐5  are  discharged  with  30  minutes  of  arriving.    With  EDIT  &  i-‐STAT  this  is  increased  to  10%  with  the  addi;onal  benefit  of  being  seen  by  a  consultant.  

    Results

    Reduces Overcrowding

    Frees up time to Care

    031778 Rev A 1/14 For In Vitro Diagnostic 13

  • With  Tradi;onal  Model  11.4%  of  pa;ents  seen  in  ED  Central  Area  Monday  to  Friday  9-‐5  return  within  7  days  of  their  ini;al  presenta;on    With  EDIT  &  i-‐STAT  this  is  9.1%    Shorter  pa;ent  journey  ;mes  do  not  equate  to  more  pa;ents  having  to  return  to  the  ED  within  7  days  

    Results

    031778 Rev A 1/14 For In Vitro Diagnostic 14

  •          

     360  ED  a_endances  per  day  cross  site  

     2.5%  reduc;on  =  9  few  admissions  per  day  

     

           

    Rates of Admission

    Old System 21.5%

    Old System & i-STAT 21.7%

    EDIT & i-STAT 19.0%

    031778 Rev A 1/14 For In Vitro Diagnostic 15

  • Introduc;on  of  a  consultant-‐led  assessment  process  (EDIT)  and  POCT  provides:  

     • 40%  reduc;on  in  the  median  ;me  from  pa;ent  arrival  to  being  declared  ‘ED  Ready’    • 2.5%  reduc;on  in  the  median  number  of  pa;ents  admi_ed  

    Conclusion

    031778 Rev A 1/14 For In Vitro Diagnostic 16

  • (CG4+)  Lactate  The  test  for  lactate,  as  part  of  the  i-‐STAT  System,  is  intended  for  use  in  the  in  vitro  quan;fica;on  of  lactate  in  arterial,  venous,  or  capillary  whole  blood.    The  i-‐STAT  lactate  test  is  useful  for  (1)  the  diagnosis  and  treatment  of  lac;c  acidosis  in  conjunc;on  with  measurements  of  blood  acid/base  status,  (2)  monitoring  ;ssue  hypoxia  and  strenuous  physical  exer;on,  and  (3)  diagnosis  of  hyperlactatemia.  

    031778 Rev A 1/14 For In Vitro Diagnostic 17

    Intended Use Information