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Functional Echocardiography
                Targeted neonatal echocardiography (TNE)
               Point of care echocardiography (POCT ECHO)

                                               Kyiv March 2013




                                                     Jan Širc

          Institute for the Care of Mother and Child, Prague, Czech Republic
          Third Faculty of Medicine, Charles University, Prague, Czech Republic




The HIP Trial is funded by the European Commission within the 7th Framework Programme
Why should we be able to perform
and interpret TNE

• Rule out structural abnormality
• Need for direct measure of cardiovascular
  function
• Effect of treatment
• Need for serial assessments
• Poor availability of cardiologists 24/7




 The HIP Trial is funded by the European Commission within the 7th Framework Programme
Increasing use of TNE in NICU
Enough of theoretical informations


Need for good training !




www.neonatalechoskills.com

The HIP Trial is funded by the European Commission within the 7th Framework Programme
The HIP Trial is funded by the European Commission within the 7th Framework Programme
Basic rules of TNE

• Find a supervisor
  - neonatologist with experience in TNE
  - pediatric cardiologist
• 24/7 access to ultrasound machine
• Congenital heart defect has to be excluded in the
  first scan




 The HIP Trial is funded by the European Commission within the 7th Framework Programme
Indications for TNE

• Suspected patent ductus arteriosus (PDA)
• The cyanosed newborn
  - suspected persistent pulmonary hypertension
  - excluding structural heart disease
• The infant with heart failure, hypotension or shock
• Newborn with heart murmur
• Central line placement
• Suspected effusion
• Suspected thrombosis



 The HIP Trial is funded by the European Commission within the 7th Framework Programme
Components of TNE

•     Left ventricular function
•     Right ventricular function
•     Ductal shunting
•     Atrial shunting
•     Pulmonary artery pressure
•     Measurement of blood flow and cardiac output
•     Superior vena cava flow

Not all have to be part of standard TNE ECHO




    The HIP Trial is funded by the European Commission within the 7th Framework Programme
LV systolic function – Fractional shortening

 •      FS – derived from an long-axis or short axis view
 •      M-Mode at the mitral leaflets tips
 •      Beam perpendicular to septum
 •      One of the most reproducible measurements




     The HIP Trial is funded by the European Commission within the 7th Framework Programme
LV systolic function – Fractional shortening


                   FS = [(LVEDD-LVESD)/LVEDD] x 100


 LVEDD – left ventricular end-
   diastolic diameter
 LVESD – left ventricular end-
   systolic diameter
                                                                                    LVESD   LVEDD
 Normal values
 Term babies 25-41%
 Preterm    23-40%



  The HIP Trial is funded by the European Commission within the 7th Framework Programme
LV systolic function – mVCFs


  mVCFs - Mean velocity of circumferential fiber shortening

          mVCFs = mean [(LVEDD-LVESD)/LVEDD] x LVET

LVET – left ventricular ejection
  time, from the closure to the
  opening of the mitral valve
                                                                                    LVET
Less sensitive to dimensional
  discrepancies

Normal values 1.5 ± 0.04
  circumferences/s



  The HIP Trial is funded by the European Commission within the 7th Framework Programme
LV systolic function – Ejection fraction

Ejection fraction (EF) – the proportion of ventricular contents
   ejected during systole


                  EF = [(LVEDD 3 -LVESD 3)/LVEDD 3] x 100%

• Any errors in measurements are cubed
• Changes in shape of the ventricular cavity

             Fractional shortening should be prefered




  The HIP Trial is funded by the European Commission within the 7th Framework Programme
Diastolic function – blood inflow


Ventricular filling velocities
From four chamber view
Ratio of E:A wave

                                                                                         E
                                                                                             A




 The HIP Trial is funded by the European Commission within the 7th Framework Programme
Diastolic function – blood inflow

•    Changes during the first week of life from dominance of filling during
     atrial contraction (A wave) to dominance of early contraction (E wave)

•    Progressive increase of E wave and E/A ratio

•    More pronounced in preterm infants (developmental changes,
     diastolic dysfunction after birth?)

•    Diastolic dysfunction – reduced both waves, dominant A wave

•    Unusable in high heart rates – merge of waves


                                  Normal values                    term > 0.7:1
                                     (E:A)                         preterm > 0.6:1



     The HIP Trial is funded by the European Commission within the 7th Framework Programme
LV systolic/diastolic function – MPI



• MPI (= Tei index) - Myocardial
  performance index

• From adjusted four chamber
  view – to get inflow and outflow

• Combines the isovolumic
  relaxation and contraction
  times

• Corrected for the ejection time



  The HIP Trial is funded by the European Commission within the 7th Framework Programme
LV systolic/diastolic function – MPI



• Less usable in high heart
  rates
                                                                             ICT         IRT

• Influenced by preload and
  afterload

Normal values 0.25 – 0.38
Poor systolic and/or diastolic
  function > 0.38
                                                                                   ET




 The HIP Trial is funded by the European Commission within the 7th Framework Programme
Tissue Doppler

• Systolic and diastolic function
• Measuring of myocardium movement in 4 chamber view
• 2 variables peak velocities – S´, E´, A´ wave
                time intervals – IVC, IVR, TEI index (MPI index)



                                                                                          S´




                                                                                           E´
                                                                                                A´



  The HIP Trial is funded by the European Commission within the 7th Framework Programme
Tissue Doppler




                                                              TISSUE DOPPLER ECHOCARDIOGRAPHY
                                                              ASSESSMENT OF MYOCARDIAL FUNCTION IN
                                                              EARLY NEONATAL PERIOD
                                                              Sirc J, Semberova J, Stranak Z
                                                              ECPM Paris 2013




 The HIP Trial is funded by the European Commission within the 7th Framework Programme
Other modalities

• Strain
• Strain rate
• Speckle tracking

Used in cardiology or for
  research




 The HIP Trial is funded by the European Commission within the 7th Framework Programme
Ductal shunting

• Ductal diameter
• Direction of blood flow, flow pattern – restricted, wide open
• Assesment of hemodynamic significance
  1. diastolic flow in abdominal aorta – steal or not
  2. diastolic flow in left pulmonary artery (more than 0:2 m/s)
  3. Left atrium to aortic root ratio - LA/Ao ratio (more than 1.5)
  4. Flow pattern in pulmonary artery – turbulent flow
  5. Left heart overload, mitral regurgitation




  The HIP Trial is funded by the European Commission within the 7th Framework Programme
Atrial shunting

• High incidence
• From subcostal four chamber view or short axis
  view




 The HIP Trial is funded by the European Commission within the 7th Framework Programme
Atrial shunting

• Usually low velocity flow – colour Doppler, pulsed wave

• Dominant shunting is left to right (up to 30% of right to left is
  normal)

• Pure right to left shunt – congenital heart disease, pulmonary
  hypertension of the newborn (PPHN)

• Large atrial shunting increases right ventricular output,
  decreases LA/Ao ratio




 The HIP Trial is funded by the European Commission within the 7th Framework Programme
Pulmonary artery pressure (PAP)


1. From ductal shunting

•       Ductal flow reflects relation of
        systemic and pulmonary BP

•       Derived from colour Doppler,
        pulsed/continuous Doppler

•       Supra-systemic pressure when
        right-to-left flow ≥ 30% of cardiac
        cycle

•      bidirectional PDA flow is typical for
      first hours after birth, changes to L-
      R as PVR decreases

    The HIP Trial is funded by the European Commission within the 7th Framework Programme
Pulmonary artery pressure (PAP)


2. From tricuspid regurgitation jet

•     Modified Bernoulli equation
      PAP = 4 x velocity2 + 5 (atrial
      pressure)

•     Most accurate of the indirect
      methods

•     50% of a babies will not have
      tricuspidal regurgitation




    The HIP Trial is funded by the European Commission within the 7th Framework Programme
Assessment of systemic blood flow

 • Systemic blood flow ≠ cardiac output when atrial
   and ductal shunt is present

 Ductal shunt – increases left ventricular output
 Atrial shunt – increases right ventricular output


 Blood flow

 • VTI – velocity time integral, area
   under the systolic envelope
 • Cross sectional area
 • Heart rate
 • Infants weight



  The HIP Trial is funded by the European Commission within the 7th Framework Programme
Left ventricular output - LVO


 • Measuring of ascending aorta
 • Diameter – from long axis view, end-systolic internal
   (trailing edge to leading edge) diameter beyond the
   coronary sinus
 • Velocity – from apical or suprasternal view, average VTI
   from 5 cardiac cycles

                              LVO = [p x (d2/4) x VTI x HR] / weight




 The HIP Trial is funded by the European Commission within the 7th Framework Programme
Left ventricular output - LVO




                           Normal values 150-300 ml/kg/min




 The HIP Trial is funded by the European Commission within the 7th Framework Programme
Right ventricular output - RVO

• RVO represent systemic blood flow more than LVO in preterm
  infants with PDA and FOA
• Measuring in the main pulmonary artery
• Diameter – low parasternal view, 2-D image at the insertion of
  pulm.valve leaflets in end-systole
• Velocity – just beyond the valve leaflets


                       RVO = [p x (d2/4) x VTI x HR] / weight




  The HIP Trial is funded by the European Commission within the 7th Framework Programme
Right ventricular output - RVO




                          Normal values 150-300 ml/kg/min




 The HIP Trial is funded by the European Commission within the 7th Framework Programme
Superior vena cava flow – SVC flow


• Partial cardiac input. Blood from upper body. 70-80% is from
  brain
• Not confounded by shunts
• Diameter – parasternal view before entry to right atrium
  Average value from maximal and minimal diameter
• Velocity – subcostal view. Average from 10 cycles


         SVC = [p x (d2/4) x VTI x HR] / weight


         Normal values 40-120 ml/kg/min in VLBW


  The HIP Trial is funded by the European Commission within the 7th Framework Programme
Superior vena cava flow – SVC flow


 • Diameter from parasternal view – 2D or M-mode
 • Flow – subcostal view, pulsed Doppler




 The HIP Trial is funded by the European Commission within the 7th Framework Programme
SVC flow




 The HIP Trial is funded by the European Commission within the 7th Framework Programme
Central line placement

• Appropriate placement – PICC line, UVC, UAC

• Identification of complications – thrombosis, abnormal
  position, line fracture, embolization, vessel occlusion

• Flush with normal saline may be helpful

• Advantage – routine X-Ray after insertion is not
  necessary




  The HIP Trial is funded by the European Commission within the 7th Framework Programme
Another abnormal conditions

• Suspected effusion
  pericardial - from 4 chamber view, long axis view
  pleural
  pneumopericard – unable to see the heart, echo shadow of air

• Suspected thrombosis




 The HIP Trial is funded by the European Commission within the 7th Framework Programme
Thanks a lot for your attention




The HIP Trial is funded by the European Commission within the 7th Framework Programme

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Functional Echocardiography. Targeted neonatal echocardiography (TNE). Point of care echocardiography (POCT ECHO).

  • 1. Functional Echocardiography Targeted neonatal echocardiography (TNE) Point of care echocardiography (POCT ECHO) Kyiv March 2013 Jan Širc Institute for the Care of Mother and Child, Prague, Czech Republic Third Faculty of Medicine, Charles University, Prague, Czech Republic The HIP Trial is funded by the European Commission within the 7th Framework Programme
  • 2. Why should we be able to perform and interpret TNE • Rule out structural abnormality • Need for direct measure of cardiovascular function • Effect of treatment • Need for serial assessments • Poor availability of cardiologists 24/7 The HIP Trial is funded by the European Commission within the 7th Framework Programme
  • 3. Increasing use of TNE in NICU Enough of theoretical informations Need for good training ! www.neonatalechoskills.com The HIP Trial is funded by the European Commission within the 7th Framework Programme
  • 4. The HIP Trial is funded by the European Commission within the 7th Framework Programme
  • 5. Basic rules of TNE • Find a supervisor - neonatologist with experience in TNE - pediatric cardiologist • 24/7 access to ultrasound machine • Congenital heart defect has to be excluded in the first scan The HIP Trial is funded by the European Commission within the 7th Framework Programme
  • 6. Indications for TNE • Suspected patent ductus arteriosus (PDA) • The cyanosed newborn - suspected persistent pulmonary hypertension - excluding structural heart disease • The infant with heart failure, hypotension or shock • Newborn with heart murmur • Central line placement • Suspected effusion • Suspected thrombosis The HIP Trial is funded by the European Commission within the 7th Framework Programme
  • 7. Components of TNE • Left ventricular function • Right ventricular function • Ductal shunting • Atrial shunting • Pulmonary artery pressure • Measurement of blood flow and cardiac output • Superior vena cava flow Not all have to be part of standard TNE ECHO The HIP Trial is funded by the European Commission within the 7th Framework Programme
  • 8. LV systolic function – Fractional shortening • FS – derived from an long-axis or short axis view • M-Mode at the mitral leaflets tips • Beam perpendicular to septum • One of the most reproducible measurements The HIP Trial is funded by the European Commission within the 7th Framework Programme
  • 9. LV systolic function – Fractional shortening FS = [(LVEDD-LVESD)/LVEDD] x 100 LVEDD – left ventricular end- diastolic diameter LVESD – left ventricular end- systolic diameter LVESD LVEDD Normal values Term babies 25-41% Preterm 23-40% The HIP Trial is funded by the European Commission within the 7th Framework Programme
  • 10. LV systolic function – mVCFs mVCFs - Mean velocity of circumferential fiber shortening mVCFs = mean [(LVEDD-LVESD)/LVEDD] x LVET LVET – left ventricular ejection time, from the closure to the opening of the mitral valve LVET Less sensitive to dimensional discrepancies Normal values 1.5 ± 0.04 circumferences/s The HIP Trial is funded by the European Commission within the 7th Framework Programme
  • 11. LV systolic function – Ejection fraction Ejection fraction (EF) – the proportion of ventricular contents ejected during systole EF = [(LVEDD 3 -LVESD 3)/LVEDD 3] x 100% • Any errors in measurements are cubed • Changes in shape of the ventricular cavity Fractional shortening should be prefered The HIP Trial is funded by the European Commission within the 7th Framework Programme
  • 12. Diastolic function – blood inflow Ventricular filling velocities From four chamber view Ratio of E:A wave E A The HIP Trial is funded by the European Commission within the 7th Framework Programme
  • 13. Diastolic function – blood inflow • Changes during the first week of life from dominance of filling during atrial contraction (A wave) to dominance of early contraction (E wave) • Progressive increase of E wave and E/A ratio • More pronounced in preterm infants (developmental changes, diastolic dysfunction after birth?) • Diastolic dysfunction – reduced both waves, dominant A wave • Unusable in high heart rates – merge of waves Normal values term > 0.7:1 (E:A) preterm > 0.6:1 The HIP Trial is funded by the European Commission within the 7th Framework Programme
  • 14. LV systolic/diastolic function – MPI • MPI (= Tei index) - Myocardial performance index • From adjusted four chamber view – to get inflow and outflow • Combines the isovolumic relaxation and contraction times • Corrected for the ejection time The HIP Trial is funded by the European Commission within the 7th Framework Programme
  • 15. LV systolic/diastolic function – MPI • Less usable in high heart rates ICT IRT • Influenced by preload and afterload Normal values 0.25 – 0.38 Poor systolic and/or diastolic function > 0.38 ET The HIP Trial is funded by the European Commission within the 7th Framework Programme
  • 16. Tissue Doppler • Systolic and diastolic function • Measuring of myocardium movement in 4 chamber view • 2 variables peak velocities – S´, E´, A´ wave time intervals – IVC, IVR, TEI index (MPI index) S´ E´ A´ The HIP Trial is funded by the European Commission within the 7th Framework Programme
  • 17. Tissue Doppler TISSUE DOPPLER ECHOCARDIOGRAPHY ASSESSMENT OF MYOCARDIAL FUNCTION IN EARLY NEONATAL PERIOD Sirc J, Semberova J, Stranak Z ECPM Paris 2013 The HIP Trial is funded by the European Commission within the 7th Framework Programme
  • 18. Other modalities • Strain • Strain rate • Speckle tracking Used in cardiology or for research The HIP Trial is funded by the European Commission within the 7th Framework Programme
  • 19. Ductal shunting • Ductal diameter • Direction of blood flow, flow pattern – restricted, wide open • Assesment of hemodynamic significance 1. diastolic flow in abdominal aorta – steal or not 2. diastolic flow in left pulmonary artery (more than 0:2 m/s) 3. Left atrium to aortic root ratio - LA/Ao ratio (more than 1.5) 4. Flow pattern in pulmonary artery – turbulent flow 5. Left heart overload, mitral regurgitation The HIP Trial is funded by the European Commission within the 7th Framework Programme
  • 20. Atrial shunting • High incidence • From subcostal four chamber view or short axis view The HIP Trial is funded by the European Commission within the 7th Framework Programme
  • 21. Atrial shunting • Usually low velocity flow – colour Doppler, pulsed wave • Dominant shunting is left to right (up to 30% of right to left is normal) • Pure right to left shunt – congenital heart disease, pulmonary hypertension of the newborn (PPHN) • Large atrial shunting increases right ventricular output, decreases LA/Ao ratio The HIP Trial is funded by the European Commission within the 7th Framework Programme
  • 22. Pulmonary artery pressure (PAP) 1. From ductal shunting • Ductal flow reflects relation of systemic and pulmonary BP • Derived from colour Doppler, pulsed/continuous Doppler • Supra-systemic pressure when right-to-left flow ≥ 30% of cardiac cycle • bidirectional PDA flow is typical for first hours after birth, changes to L- R as PVR decreases The HIP Trial is funded by the European Commission within the 7th Framework Programme
  • 23. Pulmonary artery pressure (PAP) 2. From tricuspid regurgitation jet • Modified Bernoulli equation PAP = 4 x velocity2 + 5 (atrial pressure) • Most accurate of the indirect methods • 50% of a babies will not have tricuspidal regurgitation The HIP Trial is funded by the European Commission within the 7th Framework Programme
  • 24. Assessment of systemic blood flow • Systemic blood flow ≠ cardiac output when atrial and ductal shunt is present Ductal shunt – increases left ventricular output Atrial shunt – increases right ventricular output Blood flow • VTI – velocity time integral, area under the systolic envelope • Cross sectional area • Heart rate • Infants weight The HIP Trial is funded by the European Commission within the 7th Framework Programme
  • 25. Left ventricular output - LVO • Measuring of ascending aorta • Diameter – from long axis view, end-systolic internal (trailing edge to leading edge) diameter beyond the coronary sinus • Velocity – from apical or suprasternal view, average VTI from 5 cardiac cycles LVO = [p x (d2/4) x VTI x HR] / weight The HIP Trial is funded by the European Commission within the 7th Framework Programme
  • 26. Left ventricular output - LVO Normal values 150-300 ml/kg/min The HIP Trial is funded by the European Commission within the 7th Framework Programme
  • 27. Right ventricular output - RVO • RVO represent systemic blood flow more than LVO in preterm infants with PDA and FOA • Measuring in the main pulmonary artery • Diameter – low parasternal view, 2-D image at the insertion of pulm.valve leaflets in end-systole • Velocity – just beyond the valve leaflets RVO = [p x (d2/4) x VTI x HR] / weight The HIP Trial is funded by the European Commission within the 7th Framework Programme
  • 28. Right ventricular output - RVO Normal values 150-300 ml/kg/min The HIP Trial is funded by the European Commission within the 7th Framework Programme
  • 29. Superior vena cava flow – SVC flow • Partial cardiac input. Blood from upper body. 70-80% is from brain • Not confounded by shunts • Diameter – parasternal view before entry to right atrium Average value from maximal and minimal diameter • Velocity – subcostal view. Average from 10 cycles SVC = [p x (d2/4) x VTI x HR] / weight Normal values 40-120 ml/kg/min in VLBW The HIP Trial is funded by the European Commission within the 7th Framework Programme
  • 30. Superior vena cava flow – SVC flow • Diameter from parasternal view – 2D or M-mode • Flow – subcostal view, pulsed Doppler The HIP Trial is funded by the European Commission within the 7th Framework Programme
  • 31. SVC flow The HIP Trial is funded by the European Commission within the 7th Framework Programme
  • 32. Central line placement • Appropriate placement – PICC line, UVC, UAC • Identification of complications – thrombosis, abnormal position, line fracture, embolization, vessel occlusion • Flush with normal saline may be helpful • Advantage – routine X-Ray after insertion is not necessary The HIP Trial is funded by the European Commission within the 7th Framework Programme
  • 33. Another abnormal conditions • Suspected effusion pericardial - from 4 chamber view, long axis view pleural pneumopericard – unable to see the heart, echo shadow of air • Suspected thrombosis The HIP Trial is funded by the European Commission within the 7th Framework Programme
  • 34. Thanks a lot for your attention The HIP Trial is funded by the European Commission within the 7th Framework Programme