Predicon,prevenonandtreatmentof...

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2011-05-28 1 www.rop.gu.se Ann Hellström, MD, PhD Predic’on, preven’on and treatment of Re’nopathy Of Prematurity Institute of Neuroscience and Physiology, Department of Ophthalmology, The Sahlgrenska Academy at University of Gothenburg, Sweden Evidence-based neonatology – today and tomorrow www.rop.gu.se

Transcript of Predicon,prevenonandtreatmentof...

Page 1: Predicon,prevenonandtreatmentof Re’nopathy+Of+Prematurity+ebneo.org/documents/USB_mem/8.Lectures_5_June/1_ROP.pdf · 2011-05-28 1 Ann Hellström, MD, PhD Predicon,prevenonandtreatmentof

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Ann Hellström, MD, PhD

Predic'on,  preven'on  and  treatment  of  Re'nopathy  Of  Prematurity  

Institute of Neuroscience and Physiology, Department of Ophthalmology,

The Sahlgrenska Academy at University of Gothenburg, Sweden

Evidence-based neonatology – today and tomorrow

www.rop.gu.se

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Re'nopathy  of  prematurity  (ROP)  

Re#nal  disease                                  Visual  loss    

Phase I ROP impaired vessel

growth & vessel loss

Phase II ROP pathological

neovascularization

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ROP  -­‐  historically   (Gilbert, Early Hum Dev 2008, 84:77-82)

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Screening-­‐criteria  based  on  GA  &  BW  

 GA  (weeks)   BW  (grams)  

Sweden   <  32   (<  1500g)  

USA   <  32*   <  1500*  

UK   <  32   <  1501  

Turkey   <  34   <  1850  

Romania   <  34   <  2000  

China   <  34   <  2000  

Brazil   <  32  or  <  35!   <  1500  

* Sick more mature infants are also screened

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Screening  examina'ons  are  stressful,  painful  and  resource  consuming    -­‐  altera#ons  in  blood  pressure  &  heart  rate  -­‐  decreased  oxygen  satura#on  -­‐  increased  cor#sol  levels  for  up  to  24h      

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Conclusion  

•   Na#onal  guidelines  based  on  GA  and  BW,  although  postnatal  factors  of  utmost  importance  for  ROP  

•   Only  5-­‐10%  of  screened  children  need  treatment  •   Other  selec#on  criteria  than  GA  and  BW  are  needed  in  order  to  reduce  unnecessary  examina#ons  

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Weight  IGF-­‐I  Neonatal  Re#nopathy  Of  Prematurity  

WINROP  

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So  what  does  WINROP  do?  

It  calculates  and  accumulates  each  week    the  infants  devia#on  

from  its  op#mal  growth  velocity  curve  

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WINROP

                 Model  with  Weight  only

Sensi#vity Specificity

Swedish  infants  (n=374) 100% 85%

American  infants  (n=318)   100%   82%  

Brazilian  infants    (n=366)   90%   55%  

Swiss  infants  (n=376)   100%   81%  

Published  WINROP  outcome  

Hellström  A  et  al  Pediatrics  2009,  Wu  C  et  al,  Hård  A-­‐L  et  al  Arch  Ophthalmol  2010,    Fluckiger  S  et  al  Klin  Monobl  Augenheikld  2011  

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Risk  for  Type  1  ROP  aTer  alarm  in  WINROP  

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Reduce  screening  significantly    and  focus  on  the  right  pa'ents  

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Hellström  A  et  al  Pediatrics  2009  

New  pathogene'c  mechanisms….  

Chronological Age (weeks after birth) PMA > 40 weeks

Här  skall  nyZ  ’simplified  confusogram’  in  

10  9  8  7  6  5  4  3  2  1  0  

WINROP  iden'fies  risk  of  developing  ROP   Ophthalmologist  applies  “destruc've”  

treatment  

Ophthalmologist  diagnosis  ROP  

Period  for  ophthalmological  screening  

Chronological Age (weeks after birth)

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Today’s  treatment  of  ROP  

Re#nal  disease                            Visual  loss    

Phase I ROP impaired vessel growth &

vessel loss

Phase II ROP pathological

neovascularization

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New  treatments  for  ROP  

•   Avas#n  (bevacizumab)  –An#  VEGF  •   Propranolol  •   Inositol  •   Erythropoie#n    

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Bevacizumab  (1.25  mg/50µL)  intravitreal  injec#on  one  Macaque  eye  Miyake  et  al.Invest  Ophth  Vis  Sci  2010    

3 male macaques 8-9 years old 3.9-5.5 kg

www.rop.gu.se ©  The  Ophthalmic  Communica#ons  Society,  Inc.    Published  by  Lippincoi  Williams  &  Wilkins,  Inc.   2  

VITREOUS  AND  PLASMA  CONCENTRATIONS  OF  APELIN  AND  VASCULAR  ENDOTHELIAL  GROWTH  FACTOR  AFTER  INTRAVITREAL  BEVACIZUMAB  IN  EYES  WITH  PROLIFERATIVE  DIABETIC  RETINOPATHY.  Qian,  Jing;  Lu,  Qiang;  Tao,  Yong;  MD,  PhD;  Jiang,  Yan-­‐Rong    Re#na.  31(1):161-­‐168,  January  2011.  DOI:  10.1097/IAE.0b013e3181e46ad8  

Fig.  2  .  Boxplots  showing  the  plasma  concentra#ons  of  VEGF  in  the  bevacizumab  study  group  undergoing  pars  plana  vitrectomy  for  PDR  aqer  IVB  and  a  control  group  undergoing  vitrectomy  without  previous  IVB;  the  difference  between  both  groups  was  significant  (P  =  0.003).  

1.25  mg  bevacizumab  was  injected  into  the  vitreous  of  one  eye  7  days  previously  

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Tomorrows  treatment  of  ROP  -­‐  preven'on?  

Phase I ROP impaired vessel growth &

vessel loss

Phase II ROP pathological

neovascularization

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Preven'on  -­‐  oxygen  A  majority  of  studies  have  shown  that  a  satura#on  between  85-­‐93%  results  in  reduc#on  of  severe  ROP    SUPPORT  study    

 –  85-­‐89%  oxygen  resulted  in  reduc#on  of  ROP  but    increased  mortality  (one  addi#onal  death  for  every    two  saving  severe  ROP...)  

 STOP-­‐ROP  and  BOOST  study    

 -­‐  supplemental  oxygen  at  prethreshold  decrease  non  PLUS  ROP  but  increased  pulmonary  morbidity      Compliance  poor  with  lower  oxygen  levels      

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Preven'on  -­‐  nutri'on  Few  studies  have  shown  that  op#mal  nutri#on  results  in  reduc#on  of  severe  ROP    Fish-­‐oil  fat  supplementa#on    

 –  reduced  risk  of  laser  treatment  (Pediatrics  Jan  2011)    Human  milk  vs  formula  

 -­‐  reduced  risk  for  ROP  (J  Perinatol  2001)    Cochrane  database  2005  

 -­‐  not  conclusive  for  recommenda#on      

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Preven'on  –  op'mize  growth  

IGF-­‐I  and  fetal  growth    IGF-­‐I  associated  with  ini#al  weight  loss    IGF-­‐I  enhance  protein  u#lisa#on    IGF-­‐I  improves  metabolic  control    

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Phase  II  –  Study  (ROPP-­‐2009-­‐01)  

•   Longitudinal  infusion  1-­‐8  weeks  (un#l  intrauterine  levels  reached)  •   Mul#center  study  (Lund,  Gothenburg  &  Stockholm)  

•   45+45  infants  •   Study  started  June  2010  and  is  ongoing  •   First  sec#on  completed  June  2011  (n=5)  

 

 

A  Phase  II,  Open-­‐Label,  Mul'center,  Dose  Evalua'on  Study  to  Determine    safety  and  efficacy  of  rhIGF-­‐I/rhIGFBP-­‐3  in  Premature  Infants  

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Phase  II  –  Study  (ROPP-­‐2009-­‐01)  A  Phase  II,  Open-­‐Label,  Mul'center,  Dose  Evalua'on  Study  to  Determine    

safety  and  efficacy  of  rhIGF-­‐I/rhIGFBP-­‐3  in  Premature  Infants  

Primary  Efficacy  Endpoints:            Severity  of  ROP      Secondary  Efficacy  Endpoints:          Brain  development        -­‐  MRI  at  40  weeks  PMA          -­‐  cogni#ve  outcome  at  2.5,  6  and  10  years        Metabolism      Body  weight      Length      Incidence  of  BPD      Days  in  NICU          

 

 

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Coworkers  Anna-­‐Lena  Hård    

Chatarina  Löfqvist  David  Ley  

Ingrid  Hansen  Pupp    Eva  Andersson  

Gunnel  Hellgren    Aimon  Niklasson  

Margareta  Hök  Wikstrand  Carola  Pfeiffer-­‐Mosesson  

Lois  Smith