1 Nuclear Medicine Quality control. 2 Uniformity gamma camera E + L + Flood correctie Energy...

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1

Nuclear Medicine

Quality control

2

Uniformity gamma camera

E + L + Flood correctie

Energy correctionNo correction

E + Linearity

divide by flood source image

3

Uniformity PET camera

sinogram

projection

Uncorrected Corrected

Blank scan

Correction: energyuniformitydead time

4

QC gamma camera

Planar• uniformity• energy resolution• linearity• spatial resolution• dead time• sensitivity• pixel size

Whole Body• bed motion• uniformity• pixel size

SPECT• center of rotation• detector position• Phantom

5

dead time

• straightforward: decaying source

• two sources with (nearly) same activity

6

Center of rotation

7

Detector position

8

well counterdose calibratorsurvey meter

9

NaI(Tl)

PMT

lead

shi

eldi

ng

well counter

10

NaI(Tl)

PMT

lead

shi

eldi

ng

D

H

Ra

sens =

D

sensitivity

well counter

gas filled detectors

11

+

- - -

- - -

-+++

--

applied voltage

output current

ionizationchamber

proportionalcounter

Geiger-Müller

dose calibrator

12

isotope selection

dose calibrator

13

+

- - -

- - -

-+++

--

output current = const x air kerma (or Ar kerma)

+-

function of isotope energy!

dose calibrator

14

with Cu filter

survey meters

15

ionisation detector (Xenon)

survey meters

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scintillator (NaI(Tl))

contamination monitor, spectrometer

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NaI(Tl) scintillation crystal

contamination monitor

18

19

Image analysis

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SUV: standard uptake value

g in weighttotal / Bq in dose total

j in Bq/g in amount tracer

ionconcentrat tracer average

j in ionconcentrat tracerSUV j

•somewhat controversial•only valid if procedure is standard:

• time between injection and image• condition of patient• ...

•used all the time!

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example:analysis of heart images

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Image analysis

18F-FDG

13N-NH3

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perfusion + metabolism

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Gated PET

25

Partialvolume

constantactivity

big pixels

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Partialvolume

constantconcentration

finite resolution

perfect resolution

finite resolution

Recovery

Spill-over

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Partialvolume

constantactivity

finite resolution

28

Gated MIBI, thickening

7

6

5432

2 4 6 8

200400600800

1000

00

1

0

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30

Tracer kinetic modelling

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Dynamic PET

13N-NH3 perfusion study

20 s. 40 s.

3 min 20 min

Dynamic PET

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11C-acetate perfusion/oxidative metabolism study

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Kinetic modelling

Extra-vascular

Metabolized

K1

k2

k3

k4

0

0.1

0.2

0.3

0.4

0.5

0.6

0.7

0 100 200 300 400 500 0

0.05

0.1

0.15

0.2

0.25

0.3

0 100 200 300 400 500

Blood

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3 comp model

C’E C’M

K’1

k’2

k’3

k’4

Glucose:

0dt

'dC P

0'C)'k'k('C'Kdt

'dCE32P1

E

0'k 4

E3M 'C'k

dt

'dC - metabolized = 0

pp32

31E3 'C'R'C

'k'k

'k'K'C'k

metabolized

C’p

35

3 comp model

CE CM

K1

k2

k3

k4

FDG:

0dt

dCP

)t(C)kk()t(CKdt

dCE32P1

E

0k4

)t(Ckdt

dCE3

M

not metabolizedbut accumulated

Cp

36

Laplace transform

Cp

37

3 comp model

CE CM

K1

k2

k3

FDG:

t

0p

32

31

t

0

)ut)(kk(p

32

21

MEI

du)u(Ckk

kK

due)u(Ckk

kK

)t(C)t(C)t(C

32

38

3 comp model

Glucose consumption:

'LC

RR

'

32

31LC1

PCkkkK

Lumped constant:

11

Motion correction

12

13

14

15

16

17

11C-Acetate

40

Tracer kinetic modelling: NH3

0

0.1

0.2

0.3

0.4

0.5

0.6

0.7

0 100 200 300 400 500

parametric modelling: acetate

42

Image quality

43

Bias and variance

moreregularisation

bias

variance

A

B

A is better than B!

which method is better?

44

Software evaluation

• nice correct• image quality is task dependent• simulation, phantom, (animal), clinical

45

Dosimetry

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Dosimetry

kgJ

Gy 11

Q(photons, electrons, positrons) = 1Q(neutrons, protons) = ..10..Q(a-particles) = 20

MIRD formalism (SNM)

47

effective dose

i

BiiiAi MEBApNQBADE /)()(

A B

48

R = 2 cm

L = 4 cm

D = 10 cmd = 2 cm

m = 0.15 /cm (140 keV)m = 0.095 /cm (511 keV)

1 MBq 123I: gamma: 0.84 of 159 keVelectron: 0.13 of 127 keVhalflife: 13 h

1 MBq 18F: 1 positron of 250 keV109 min

For organs with uptake:• 3D VOIs • pixelwise MBq/cc

measurement

=> Total organ activity

dosimetry

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Residence time (hr) for the thyroid: S1: 0.0017S2: 0.0017S3: 0.0013

residence times

Residence time (hr) for the liver: S1: 0.4567S2: 0.5310S3: 0.3940

evaluation of tracer for ORL-1 receptors in the brain

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Olinda: MC-based dosimetry

• MIRD Dose Estimate Report No. 19: Radiation Absorbed Dose Estimates from 18F-FDG

dosimetry

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background radiation: ..2.. mSv / year= 5.5 mSv / day= 0.2 mSv / hour

patient:

18F-FDG, 300 MBq 6 mSv

99mTc-MIBI 740 MBq 11 mSv

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the end