Doppler Flashcards

1
Q

What can we assess with Doppler

A
  • Instantaneous direction of blood flow along key anatomic point
  • Instantaneous velocity of blood w/I sample volume or along line of interrogation (CW)
  • Absence/presence of disturbed flow
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2
Q

Appearance of envelope: brightest zone and spectral broadening

A
  • Brightest zone of color spectrum = >RBCs
  • Flow disturbance = marked spectral broadening of the time-velocity curve
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3
Q

Define PG

A

pressure in driving chamber > receiving chamber
o Pressure of receiving chamber calculated and added to gradient to estimated driving chamber P
o Conservation of energy → calculate pressure gradient from 2 areas of the heart
 Constant volume of blood moved to specific area → ↑ pressure proximal to obstruction = α ↑ in blood flow velocity

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4
Q

Limitations of modified bernoulli

A

 Slight overestimation of PG
 Blood volume, tunnel lesions (↑ friction), blood viscosity
 Intercept angle (inaccuracy)
 Valvular insufficiency + obstruction

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5
Q

Why does Doppler derived PG overestimates PG

A

o Doppler derived PG: overestimation vs KT
 Maximal instantaneous peak pressures pre and post obstruction → not occur at same time
 Discrepancy invasive vs non invasive measurements: instantaneous gradients can be 30-40% ↑ than peak to peak
 Severe stenosis = closer to peak to peak

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6
Q

What is assessed by PW TDI

A

provides myocardial mvt
o Color M-mode TDI: Myocardial velocities analyzed along a single line

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7
Q

Applications of TDI

A

 Assessment of diastolic fct
 Myocardial synchrony
 Early detection of myocardial dysfct
 Qtfy myocardial functional reserve during stress echo for dx of CA dz

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8
Q

Limitations of PW TDI

A

 Angle dependent
 May be affected by breed, age, HR
 Not discriminate active contraction of myocardium vs passive translational motion

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9
Q

Quantitative clinical use of Doppler

A

PG
Peak velocities
Ventricular filling velocities
Regurgitant fraction
Pressure 1/2 time

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10
Q

PG estimation specifics

A
  • Normal: peak diastolic and systolic pressure at either side of a valve are equal
    o Do not occur at same time
    o Peak to peak pressure gradient = 0
     Instantaneous pressure gradient can be detected (2-10mmHg)
     Typically small, drive blood through circulation
  • RBC velocity 0.25-1.7m/s
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11
Q

Abnormal high velocity flow develop in many cardiac conditions

A

AS, PS, HOCM, MR, TR, VSD, PDA
o Pressure gradient drives blood across the narrowed/restrictive orifice
* No angle correction: may overestimate pressure gradients

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12
Q

Systolic LVP

A

systemic pressures:
o Systolic LV pressure = peripheral systolic BP in absence of LVOTO
o Peak MR jet: driving pressure = LV systolic pressure = systolic BP → expect PG close to 100mmHg

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13
Q

Systolic RVP

A

pulmonary pressures
o Systolic RV pressure = pulmonary systolic pressure in absence of PS
o Peak TR jet = RV systolic pressure = systolic PAP → expect PG close to 20-25mmHg
 Higher velocity suggestive of ↑RVP and PAPs

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14
Q

Diastolic systemic P

A

AI peak velocity = PG btwn Ao and LV during diastole → close to 50 mmHg

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15
Q

Diastolic pulmonic P

A

PI peak velocity → close to 10-15mmHg (2-2.5m/s)
o Early peak = mean PA pressure
o End diastolic peak = diastolic PA pressure

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16
Q

Ao flow profile

A

o Rapid acceleration, sharp peak
 Peak depend on SV and CSA
 Vary with ∑ activity, cardiac cycle length, sedation, obstructive lesions
o Deceleration: slower, 2x thickness of acceleration limb
o AI uncommon in healthy dogs
o STI of ventricular ejection: PEP, LVET → measured from Doppler flow

17
Q

PA flow profile

A
  • PA velocity: slower to accelerate, rounded peak
    o Velocity time integral: vary beat to beat → respiration
     Ventricular filling: ↑RV SV in inspiration
     Translational movement of the heart
    o PH: sharp, pointed peak, ↓AT, notch in deceleration
    o PI common in normal dogs, low peak
     With PH, higher velocities (higher pressures)
18
Q

Use of OT

A

estimate SV w CSA and VTI

19
Q

What is assessed by ventricular filling velocities

A

ventricular diastolic function

20
Q

Ventricular filling velocities are affected by

A

ventricular relaxation/distensibility, atrial pressure, AV pressure gradient, HR, loading conditions, ventilation, cardiac lesions

21
Q

Pattern of transmitral flow

A

Tips of opened MV
o M shaped wave form: early filling + atrial contraction
 Early filling = E wave → rapid acceleration to peak, slower deceleration
 Diastasis: minimal flow
 Atrial contraction = A wave → follows P wave
o Stronger signal if: high CO state, L to R shunt, anemia, severe MR, tachycardia
o Areas under 2 triangles = V TI → estimate relative filling fractions

22
Q

PV flow patterns

A

o Flow across PV driven by PG from PV → LA, influenced by diastolic and systolic LV fct
o Polyphasic
 2 systolic forward flow waves (S) +/- Reversal wave
* Suction form MV annulus descent
* Retrograde RV SV
 Early diastolic forward flow wave (D)
* Venoventricular PG
 Late diastolic reversal wave (ar)
* Atrial contraction
* ↑ if resistance to ventricular filling, elevated ventricular pressures, ↑atrial pressures

23
Q

IVRT

A

region of interest cross Ao and MV inlet to record interval from end of systolic flow to onset of diastolic flow

24
Q

Regurgitant fraction

A

o Flow to MV = flow to AoV
o MR: flow to MV > flow to Ao

Mitral RF = ((mitral SV – Ao SV))/(Mitral SV)

25
Q

Pressure 1/2 time AI

A

o Time for peak velocity to ↓ by ½
o AI: flow profile can indicate regurgitation severity
 Rapid decline in in AI velocity (triangular shape profile vs plateau)
* Rapid decline in Ao pressure because of diastolic runoff in AI
* LV pressure also decline and PG ↓ = ↓ regurgitation
 Diastolic ½ time: <300m/s suggest hemodynamically significant AI

26
Q

Pressure 1/2 time MR

A

o M/TV stenosis
 Severe stenosis → longer pressure ½ time
 ↓ slope → delayed early filling → persistent pressure differential → delayed MV/TV closure
 Normal MV pressure ½ time: <29 +/- 8 ms in dogs, <30ms in cats

27
Q

Shunt quantification by Doppler echo

A

Doppler flow measurements at 2 cardiac sites → determine volume of blood flow
* Ratio Qp/Qs = pulmonary blood flow/systemic blood flow

28
Q

Continuity equation

A

flow proximal = flow distal

o Mass = density (D) x volume (V) x area (A)
 Density is constant
 Q1 = V1 x A1 = V2 x A2 = Q2

29
Q

How to calculate volume of flow

A

by tracing flow profiles to determine the area under the curve (VTI)
Can be done at any of 4 valves
Can also be calculated: VTI = (Peak velocity x ET)/2

30
Q

How to calculate area

A

CSA of vessel/orifice: CSA = r2
 Radius is the diameter of the vessel/area

31
Q

Is shunt fraction affected by regurgitation and Lv dysfct

A

Unaffected

32
Q

Qp equation

A

PA CSA + VTI PA

33
Q

Qs equation

A

LVOT CSA + VTI LVOT

34
Q

SV equation

A

CSA x VTI

35
Q

CO equation

A

SV x HR

36
Q

Limitations of shunt calculation

A

o Measurements from R side: high variability
 Most likely 2nd to variability in PA measurement (poor lateral wall resolution)
o MV stroke volume: high variability
 Variability when measuring MV annulus size