Dr amol gulhane
DNB resident
CARE hospitals , hyd
inner layer of endothelium (intima)
middle layer of connective tissue, smooth muscle and elastic
fibers (media)
outer layer of connective tissue (adventitia)
 have smooth muscles that contracts & relaxes to respond
changes in blood volume.
 charac. by a reduction in blood flow and hence 02 through
the peripheral vessels
 when the need of the tissues for 02 exceeds the supply, areas
of ischemia and necrosis will develop
 
Factors that can contribute to the development of peripheral
vascular disorders :
 atherosclerotic changes
 thrombus formation
 embolization
  coagulability of blood
 hypertension
 inflammatory process/infection
Atherosclerosis
Thrombosis or embolism
Aneurysm
Intimal dissection
Pseudo-aneurysm
Arterio-venous fistula
Arteritis
Entrapment syndrome
Cystic adventitial disease
Most common cause
Arterial Insufficiency
 there is a deceased blood flow toward the tissues, producing
ischemia
 pulses are usually diminished or absent
 sharp, stabbing pain occurs because of the ischemia,
particularly with activity
ischemic ulcers and changes in the skin.
1. Age (elderly) – blood vessels become less elastic, become
thin walled and calcified –  PVR –  BP
2. Sex (male)
3. Cigarette smoking
› nicotine causes vasoconstriction and spasm of the
arteries –  circulation to the extremities
› C02 inhaled in cigarette smoke reduces 02 transport to
tissues
4. Hypertension – cause elastic tissues to be replaced by fibrous
collagen tissue  arterial wall become less distensible 
resistance to blood flow   BP
5. Hyperlipedimia – atherosclerotic plaque
6. Obesity – places added burden on the heart & blood vessels
› excess fat contribute to  venous congestion
7. Lack of physical activity
› Physical activity – promotes muscle contraction 
 venous return to the heart
› aids in development of collateral circulation
8. Emotional stress – stimulates sympathetic N.S. - peripheral
vasoconstriction   BP
9. Diabetes mellitus – changes in glucose & fat metabolism
promote the atherosclerotic process
10. Family history of arthrosclerosis
 is a disorder in which there is an arteriosclerotic narrowing or
obstruction of the inner & middle layer of the artery
 most common cause of arterial obstructive disease in the
extremities
 the lower extremities are involved more than upper
extremities
 common site of disease – femoral artery, iliac arteries,
popliteal arteries
 in a diabetic, the disease becomes more progressive, affects
the smaller arteries and often involves vessels below the knee
 Sub-diaphragmatic aorta 21 – 24 mm
 Infra-diaphragmatic aorta 17 – 20 mm
 Common iliac artery 10 – 12 mm
 External iliac artery 8 – 10 mm
 Common femoral artery 7 – 9 mm
 Superficial femoral artery 6 – 8 mm
 Popliteal artery 4 – 6 mm
 Plaque formation on the intimal wall that causes partial or
complete occlusion
 Calcification of the medial layer and a gradual loss of
elasticity  weakens the arterial walls
 predisposes to aneurysm, dilation or thrombus formation

artery is unable to transport an adequate blood volume to
the tissues during exercise or rest
 Intermittent claudication – most common
› pain during exercise disappear w/in 1-2 mins. after stopping
the exercise or resting
› the femoral artery is often affected – pain in the calf muscle
– common symptom
 pain at rest is indicative of severe disease
› In advanced arteriosclerosis obliterans  ischemia may
lead to necrosis, ulceration and gangrene – toes and distal
foot
Stage Complains
I Asymptomatic
II a
II b
Mild claudication
Moderate to severe claudication
III Ishemic rest pain
IV Ulcer or gangrene
Clinical classification
The Rutherford classification
TASC II classification of femoral and popliteal lesions
type A lesions
single stenosis ≤ 10 cm in length
single occlusion ≤ 5 cm in length
type B lesions
multiple lesions (stenoses or occlusions), each ≤ 5 cm
single stenosis or occlusion ≤ 15 cm not involving the infrageniculate popliteal artery
type C lesions
multiple stenoses or occlusions totaling > 15 cm with or without heavy calcification
recurrent stenoses or occlusions that need treatment after two endovascular
interventions
type D lesions
chronic total occlusion of the common or superficial femoral artery (> 20 cm,
involving the popliteal artery)chronic total occlusion of the popliteal artery and
proximal trifurcation vessels
 Doppler ultrasonography –
› audible tone produced in proportion to blood velocity
› measure blood flow through vessels
Ankle brachial Pressure
The systolic pressure at any level of the lower extremity can be
measured by positioning a pneumatic cuff at the desired site.
Any patent artery distal to the cuff that is accessible to Doppler
ultrasound can be used for flow detection, but the posterior
tibial (PT) and dorsalis pedis (DP) arteries are usually most
convenient.
When the cuff is inflated to above systolic pressure, the
arterial flow signal disappears. As cuff pressure
is gradually lowered to slightly below systolic pressure, the flow signal
reappears,
and the pressure at which flow resumes is
recorded as the systolic pressure
In general, measurement of ankle systolic
pressure is the most valuable physiologic
test for assessing the arterial circulation in
the lower limb.
If the pressure measured by
a cuff placed just above the malleoli is less
than that of the upper arm, proximal occlusive
disease in the arteries to the lower limb
is invariably present.
The ratio of ankle systolic pressure
to brachial systolic pressure is called the
ankle-brachial index or ABI.
In the absence of proximal arterial occlusive
disease, the ankle-brachial index is
greater than 1 .0, (mean value of 1 . 1 1
± 0.10)
values greater than 0.90 are typically
interpreted as normal.
Usually limbs with single-level occlusions have
indexes greater than 0.5, and limbs with
lesions at multiple levels have indexes less
than 0.5
Many limbs with impending gangrene
or ischemic ulceration have absent Doppler
flow signals at the ankle level.
ABPI Comment
> 1.3 Falsely high value (suspicion of medial
sclerosis)
0.9 – 1.3 Normal finding0.75 – 0.9 Mild PAD
0.4 – 0.75 Moderate PAD
< 0.4 Severe PAD
Calcification of vessel walls
Beaded appearance of color flow
Ankle pressure 280
mmHg
Brachial pressure 120
mmHg
ABPI 2.3
Falsely elevated recordings in diabetic patients
Calcified & rigid arterial walls
Narrow frequency band
Steep systolic increase
Quick drop
Early diastolic reverse flow
( of systolic flow amplitude)⅕
Late diastolic short forward flow
 Cardiac pump function Cardiac insufficiency
 Aortic valve function Aortic stenosis/insufficiency
 Course of vessel Tortuosity
 Vessel branching
 Peripheral vascular resistance Peripheral
inflammation
Polyneuropathy
Warm or cold extremity
Vaso-spastic disorders
 Hyperemic (normal PSV& normal RT*)
Exercise
Fever
Downstream infection
Temporary arterial occlusion by blood pressure
cuff
 Tardus-Parvus waveform (low PSV & longer RT)
Distal to severe stenosis or occlusion
* Rise time: Time between beginning of systole & peak systole
Normal triphasic waveform
Normal DPA at rest
Monophasic hyperemic flow
Following exercise
Monophasic waveform
Normal PSV
Normal rise time
Proximal to stenosis
The character of Doppler
signals obtained proximal to an arterial
obstruction depends on the capability of
the collateral circulation. If there are wel
ldeveloped
collaterals between the Doppler
probe and the point of obstruction, the
waveform may be relatively normal.
If the Doppler probe is placed directly over
a stenotic lesion, the signal has an
abnormally
high peak systolic frequency. This
reflects the increased flow velocity in the
stenotic segment.
At site of stenosis
When a waveform is obtained from an
arterial site distal to a stenosis or occlusion,
a single, forward velocity component is
observed, with flow remaining above the
zero baseline throughout the cardiac cycle.
The peak systolic frequency is lower than
normal, and the waveform becomes flat and
rounded
Distal to stenosis
High resistance, low volume waveform
Characteristic shoulder on systolic downstroke
Due to pulse wave reflection from distal disease
ShoulderShoulder
Tardus: Longer rise time
Parvus: Low PSV
Severe stenosis or occlusion
Tardus-Parvus waveformDamping waveform
Increased systolic rise time
Loss of pulsatility
IF superficial femoral artery is patent, a PI
less than 4 indicates a hemodynamically
significant aortoiliac lesion,
The PI of the normal
common femoral artery has a mean value of 6.7.
More distally, the PI increases to 8 in
the popliteal and 14 in the PT artery
A PI value greater than or equal to 4 is
predictive of a hemodynamically normal
aortoiliac segment.
 
Aorto-iliac: 25 %

Femoro-popliteal: 65%
Infra-popliteal: 10%
Proximal: 2 cm proximal to
stenosis
At stenosis : Same Doppler angle if
possible
Vr= psv ratio
SFA:
PSV of A 69 cm/sec
PSV of B 349 cm/sec
B / A 349 / 69 = 5
> 80% diameter
stenosis
2 severe stenoses demonstrated in SFA
Areas of color flow disturbance & aliasing (arrows)
Drop-out of color flow signal in parts of lumen
Occlusion in CIA
Reversed flow in IIA (blue) to supply flow to EIA (red)
Ultrasound cannot provide reliable imaging if there are poor
acoustic windows (eg, bowel gas attenuation, diffuse vascular
calcification, or metallic stents) or poor intrinsic echogenicity
of the tissues.
Duplex scanning is time-consuming and
inconvenient post-operatively – when the region of interest
is obscured by dressings – and removing these can involve
infection risk.
DSA is the gold-standard for diagnostic imaging of PAD patients .
It enables large field-of view
(FOV) imaging with the highest possible in-plane resolution compared to other
modalities.
Drawbacks - catheterization,
nephrotoxic contrast,
exposure to high doses of ionizing radiation.
The procedure is associated with major risks such as
allergic reactions,
infections at the site of vascular access,
iatrogenic arteriovenous fistulas,
hematomas,
dissections.
Digital subtraction angiography (DSA)
Complications are reported to occur in 0.17-7% of procedures,
depending on the
arterial viability, the size of the catheter, the experience of the
clinician, and the location of the vascular access.
Given the invasiveness of the procedure, its applications is
now limited to
patients who require a surgical or percutaneous procedure for
therapeutic purposes
•DSA is the "gold standard" to diagnose, and
often to treat vascular disease. It involves
getting detailed x-ray images of the arteries
while injecting dye directly into the arteries. For
patients with poor kidney function, a non-toxic
gas carbon dioxide can be used in place of IV
dye. Blockages can often be opened minimally
invasively during an angiogram.
LEFT CIA STENOSIS
A) A catheter has been passed from the right common femoral artery and into the
abdominal aorta during a digital subtraction
angiogram. Contrast injection through the catheter reveals minor atherosclerotic wall
abnormalities in the infrarenal aorta and the left common femoral artery
B) Lower limb images reveal diffuse atherosclerotic disease of the superfi cial femoral
and popliteal arteries of both sides, with a focal area of significant stenosis in
the right popliteal artery.
CT Angiography (CTA)
CTA enables visualization of the entire peripheral vascular
tree and offers information about
lesion length, diameter, and morphology, as well as degree
of calcification, and status of distal
runoff vessels.
A number of studies have compared CTA
to the gold-standard
DSA, showing comparable diagnostic
accuracy and high confidence in
clinical decision-making solely based on
CTA .
CTA offers evaluation of plaque, calcification, and
vascular wall, while DSA
depicts only arterial lumen.
Technical limitations ---- inability to
characterize calcified lesions, particularly in smaller
vessels, due to
beam-hardening artifacts.
Drawbacks –
radiation doze
nephrotoxicity of contrast, which
is contraindicated in patients with
decreased renal function and renal
insufficiency.
CTA image of the iliofemoral arteries.
Severe, focal stenosis (arrow) is present in
the right mid-to-distal superficial femoral
artery
MR Angiography (MRA)
CE-MRA is similar in set-up and diagnostic quality to CTA.
CE-MRA methods rely on an injection of contrast material,
which alters the magnetic
properties of blood.
Peripheral MRA is routinely performed with gadolinium
(Gd)-based contrast agents .
As vascular contrast is
relatively independent of flow-dynamics, CE-MRA can be used for large field-of-view
(FOV) imaging.
For assessment of hemodynamically significant
disease Gd-MRA has reported sensitivities of 89-99.5% and specificities of 95-99%
compared to DSA.
Advantages of CE-MRA over CTA === no ionizing radiation
ability to depict
lumen of calcified vessels.
Limitations == cost,
scan time
metal artifacts from stents and surgical clips.
Association between nephrogenic systemic fibrosis and gadolinium
contrast has limited the applicability of CE-MRA in kidney disease patients.
Among the imaging modalities used in PAD evaluation, usg has
no contraindications for patient with renal insufficiency.
Ultrasonography alone is
inadequate for planning of surgical procedures because it does
not provide accurate visualization
of the entire peripheral vascular tree.
Among the remaining modalities, both DSA and CTA,
given their exposure to nephrotoxic contrast material and ionizing
radiation, are unsafe for kidney disease patients.
Recent association between nephrogenic systemic
fibrosis and gadolinium contrast has challenged the safety of CE-
MRA as well
Contrastenhanced
peripheral
MRA
Symptomatic iliac artery occlusive disease, diagnosed with gadolinium-enhanced MR
angiography. (a) Coronal MIP image from a gadolinium-enhanced 3D MR angiographic
study performed with administration of gadopentetate dimeglumine demonstrates bilateral
severe proximal iliac artery stenoses, with the right greater thanthe left (arrows).
(b) The next anatomic station was imaged 10 minutes after the preceding study with a
second dose of gadopentetate Dimeglumine by using a slightly faster sequence. There is
Unlike DU, MRA
allows simultaneous angiographic as well as anatomical
volume acquisition of the whole body in seconds whilst
maintaining high spatial resolution.
This allows both luminal
and extra-luminal pathology to be shown simultaneously,
although magnetic resonance imaging is poorer for bony
anatomy than computed tomography
Like DSA, contrast enhanced magnetic resonance imaging is
sensitive to patient motion artefacts. If there is patient motion
between the mask acquisition and postcontrast acquisition,
there will be image degradation following subtraction.
Magnetic resonance cannot image calcification or steel
stents; causes susceptibility artefacts
recognizable as signal voids in the image.
Metallic structures
within the vessel lumen or adjacent to the vessel may cause
magnetic susceptibility artefacts that obscure the vessel lumen
leading to a false diagnosis of a stenosis or obstruction.
Non-Contrast Magnetic Resonance
Techniques for Peripheral Angiography
In recent years there has been a renewed interest in unenhanced
techniques, determined by two major factors.
(1) improvements in MRI hardware and software have
reduced acquisition times and made non-contrast imaging clinically
practical
(2) concerns about NSF in advanced renal disease patients
Non-contrast MRA techniques rely on flow-induced
changes in the longitudinal or
transverse magnetization of blood to obtain contrast
between the vasculature and stationary
background without administration of exogenous contrast
material.
Four major approaches for
artery-background contrast generation exist:
(1) Time-of-flight techniques (TOF) rely on differences in exposure
to radiofrequency
excitation between stationary tissue within the volume of interest and
blood protons
flowing into the imaging slab from outside the FOV.
(2) Phase-contrast MRA relays on measurable velocity-
induced changes in the phase of
the blood signal
(3) ECG-triggered subtraction techniques relay on the
difference in arterial flow velocity
between systole and diastole; either gradient echo or fast
spin-echo read out can be
used
(4) Flow-independent angiography uses an acquisition
that naturally provides bright blood
signal weighting, combined with inversion-recovery and T2
preparation to null
the signal of background tissues.
Currently, the MR angiographic approach
to the tibial vessels is dominated
by the use of TOF techniques
This flow-dependent strategy circumvents
the challenge of achieving a sufficient
concentration of contrast medium
to effectively demonstrate the distal arterial
Vessels.
At present, TOF imaging
offers the surgeon sufficient information
to make the primary surgical decisions
Overestimation of segmental occlusions with TOF imaging. (a) Coronal MIP image
obtained with TOF imaging demonstrates bilateral iliac artery occlusions, with right
greater than left.
(b) MIP image from a gd-enhanced 3D MR angiogram shows a shorter length of
each occlusion compared with a.
The depiction of the right hypogastric artery which was not seen with TOF imaging.
Suppression of thesignal from retrograde flow is a major limitation of TOF strategies
designed to eliminate venous
signal.
Vascular calcifications in a patient with diabetes mellitus. A, Coronal thin
section maximum intensity projection (MIP) of a computed tomography
angiography of the tibial peroneal runoff vessels demonstrating how dense
calcifications in this patient population obscures analysis of the lumen.
B, Contrast-enhanced magnetic resonance angiography is insensitive to
vascular calcification as well as bone, simplifying image interpretation as
demonstrated in this full-volume MIP from the same patient as in A.
– directed toward prevention of vessel occlusion
 use of vasodilators
Surgical intervention – in advanced disease – ischemic changes
and pain severely impairs activity
 Embolectomy
› removal of a blood clot, done when large arteries are
obstructed
 Endarterectomy
› is removal of a blood clot and stripping of atherosclerotic
plaque along with the inner arterial wall.
 Arterial by-pass surgery
› an obstructed arterial segment may be bypassed by
using a prosthetic material (Teflon) or the pt’s. own artery
or vein (saphenous vein)
Primary treatment strategy according
TASC severity
TASC A - endovascular therapy
TASC B - endovascular therapy
TASC C - surgical therapy (if patient is able
to be operated, otherwise endovascular
therapy)
TASC D - surgical therapy
Endarterectomy
 Percutaneous Transluminal Angioplasty
› The balloon tip of the catheter is inflated to provide
compression of the plaque
 Amputation
› with advanced atherosclerosis & gangrene of extremities
› toes are the most often amputated part of the body
FA lumen filled with hypoechoic thrombus or embolus
Good delineation of vessel wall without signs of plaque
Normal flow in adjacent FV
.
Aneurysm
Diameter increase > 50% of normal expected
diameter
Ectasia
Diameter increase < 50% of normal expected
diameter
Considerable variability in normal diameter of
arteries
Depends on physical size, sex, & age
Considerable variability in normal diameter of
arteries
Depends on physical size, sex, & age
.
True aneurysm
False aneurysm
Dissecting aneurysm
.
Sonography is the recommended non-
invasive
technique for the postoperative
monitoring
of bypass graft patency
Sonography is the recommended non-
invasive
technique for the postoperative
monitoring
of bypass graft patency
 Synthetic graft
PTFE* Above knee
 Autologous vein
* PTFE: Polytetrafluoroethylene
Aorto-bi-femoral graft Femoral-to-femoral artery bypass graft
Peripheral arterial bypass graft – 1
Femoro-Popliteal
Above Knee
Femoro-Popliteal
Below Knee
Femoro-Tibial
Below Knee
Composite PTFE & vein graft
Slightly dilated area
corresponding to valve site
In situ vein graft
Hyperemic flow often seen
in early postoperative period
Hyperemic monopahasic flow Pulsatile flow
Over time, flow normally
assumes a pulsatile flow
Average PSV
from 3 – 4 sites
without stenosis
Graft flow velocity
Normal PSV: 45 – 180 cm/s

Atherosclerosis
 Graft
degeneration

Neointimal
hyperplasia
 Technical
faults
Amol gulhane -peripheral vascular disease

Amol gulhane -peripheral vascular disease

  • 1.
    Dr amol gulhane DNBresident CARE hospitals , hyd
  • 2.
    inner layer ofendothelium (intima) middle layer of connective tissue, smooth muscle and elastic fibers (media) outer layer of connective tissue (adventitia)  have smooth muscles that contracts & relaxes to respond changes in blood volume.
  • 3.
     charac. bya reduction in blood flow and hence 02 through the peripheral vessels  when the need of the tissues for 02 exceeds the supply, areas of ischemia and necrosis will develop   Factors that can contribute to the development of peripheral vascular disorders :  atherosclerotic changes  thrombus formation  embolization   coagulability of blood  hypertension  inflammatory process/infection
  • 4.
    Atherosclerosis Thrombosis or embolism Aneurysm Intimaldissection Pseudo-aneurysm Arterio-venous fistula Arteritis Entrapment syndrome Cystic adventitial disease Most common cause
  • 5.
    Arterial Insufficiency  thereis a deceased blood flow toward the tissues, producing ischemia  pulses are usually diminished or absent  sharp, stabbing pain occurs because of the ischemia, particularly with activity ischemic ulcers and changes in the skin.
  • 6.
    1. Age (elderly)– blood vessels become less elastic, become thin walled and calcified –  PVR –  BP 2. Sex (male) 3. Cigarette smoking › nicotine causes vasoconstriction and spasm of the arteries –  circulation to the extremities › C02 inhaled in cigarette smoke reduces 02 transport to tissues 4. Hypertension – cause elastic tissues to be replaced by fibrous collagen tissue  arterial wall become less distensible  resistance to blood flow   BP 5. Hyperlipedimia – atherosclerotic plaque 6. Obesity – places added burden on the heart & blood vessels › excess fat contribute to  venous congestion
  • 7.
    7. Lack ofphysical activity › Physical activity – promotes muscle contraction   venous return to the heart › aids in development of collateral circulation 8. Emotional stress – stimulates sympathetic N.S. - peripheral vasoconstriction   BP 9. Diabetes mellitus – changes in glucose & fat metabolism promote the atherosclerotic process 10. Family history of arthrosclerosis
  • 8.
     is adisorder in which there is an arteriosclerotic narrowing or obstruction of the inner & middle layer of the artery  most common cause of arterial obstructive disease in the extremities  the lower extremities are involved more than upper extremities  common site of disease – femoral artery, iliac arteries, popliteal arteries  in a diabetic, the disease becomes more progressive, affects the smaller arteries and often involves vessels below the knee
  • 10.
     Sub-diaphragmatic aorta21 – 24 mm  Infra-diaphragmatic aorta 17 – 20 mm  Common iliac artery 10 – 12 mm  External iliac artery 8 – 10 mm  Common femoral artery 7 – 9 mm  Superficial femoral artery 6 – 8 mm  Popliteal artery 4 – 6 mm
  • 11.
     Plaque formationon the intimal wall that causes partial or complete occlusion  Calcification of the medial layer and a gradual loss of elasticity  weakens the arterial walls  predisposes to aneurysm, dilation or thrombus formation  artery is unable to transport an adequate blood volume to the tissues during exercise or rest
  • 12.
     Intermittent claudication– most common › pain during exercise disappear w/in 1-2 mins. after stopping the exercise or resting › the femoral artery is often affected – pain in the calf muscle – common symptom  pain at rest is indicative of severe disease › In advanced arteriosclerosis obliterans  ischemia may lead to necrosis, ulceration and gangrene – toes and distal foot
  • 13.
    Stage Complains I Asymptomatic IIa II b Mild claudication Moderate to severe claudication III Ishemic rest pain IV Ulcer or gangrene Clinical classification The Rutherford classification
  • 14.
    TASC II classificationof femoral and popliteal lesions type A lesions single stenosis ≤ 10 cm in length single occlusion ≤ 5 cm in length type B lesions multiple lesions (stenoses or occlusions), each ≤ 5 cm single stenosis or occlusion ≤ 15 cm not involving the infrageniculate popliteal artery type C lesions multiple stenoses or occlusions totaling > 15 cm with or without heavy calcification recurrent stenoses or occlusions that need treatment after two endovascular interventions type D lesions chronic total occlusion of the common or superficial femoral artery (> 20 cm, involving the popliteal artery)chronic total occlusion of the popliteal artery and proximal trifurcation vessels
  • 16.
     Doppler ultrasonography– › audible tone produced in proportion to blood velocity › measure blood flow through vessels
  • 17.
    Ankle brachial Pressure Thesystolic pressure at any level of the lower extremity can be measured by positioning a pneumatic cuff at the desired site. Any patent artery distal to the cuff that is accessible to Doppler ultrasound can be used for flow detection, but the posterior tibial (PT) and dorsalis pedis (DP) arteries are usually most convenient. When the cuff is inflated to above systolic pressure, the arterial flow signal disappears. As cuff pressure is gradually lowered to slightly below systolic pressure, the flow signal reappears, and the pressure at which flow resumes is recorded as the systolic pressure
  • 18.
    In general, measurementof ankle systolic pressure is the most valuable physiologic test for assessing the arterial circulation in the lower limb. If the pressure measured by a cuff placed just above the malleoli is less than that of the upper arm, proximal occlusive disease in the arteries to the lower limb is invariably present. The ratio of ankle systolic pressure to brachial systolic pressure is called the ankle-brachial index or ABI.
  • 19.
    In the absenceof proximal arterial occlusive disease, the ankle-brachial index is greater than 1 .0, (mean value of 1 . 1 1 ± 0.10) values greater than 0.90 are typically interpreted as normal. Usually limbs with single-level occlusions have indexes greater than 0.5, and limbs with lesions at multiple levels have indexes less than 0.5 Many limbs with impending gangrene or ischemic ulceration have absent Doppler flow signals at the ankle level.
  • 21.
    ABPI Comment > 1.3Falsely high value (suspicion of medial sclerosis) 0.9 – 1.3 Normal finding0.75 – 0.9 Mild PAD 0.4 – 0.75 Moderate PAD < 0.4 Severe PAD
  • 22.
    Calcification of vesselwalls Beaded appearance of color flow Ankle pressure 280 mmHg Brachial pressure 120 mmHg ABPI 2.3 Falsely elevated recordings in diabetic patients Calcified & rigid arterial walls
  • 23.
    Narrow frequency band Steepsystolic increase Quick drop Early diastolic reverse flow ( of systolic flow amplitude)⅕ Late diastolic short forward flow
  • 25.
     Cardiac pumpfunction Cardiac insufficiency  Aortic valve function Aortic stenosis/insufficiency  Course of vessel Tortuosity  Vessel branching  Peripheral vascular resistance Peripheral inflammation Polyneuropathy Warm or cold extremity Vaso-spastic disorders
  • 26.
     Hyperemic (normalPSV& normal RT*) Exercise Fever Downstream infection Temporary arterial occlusion by blood pressure cuff  Tardus-Parvus waveform (low PSV & longer RT) Distal to severe stenosis or occlusion * Rise time: Time between beginning of systole & peak systole
  • 27.
    Normal triphasic waveform NormalDPA at rest Monophasic hyperemic flow Following exercise
  • 28.
  • 29.
    Proximal to stenosis Thecharacter of Doppler signals obtained proximal to an arterial obstruction depends on the capability of the collateral circulation. If there are wel ldeveloped collaterals between the Doppler probe and the point of obstruction, the waveform may be relatively normal.
  • 30.
    If the Dopplerprobe is placed directly over a stenotic lesion, the signal has an abnormally high peak systolic frequency. This reflects the increased flow velocity in the stenotic segment. At site of stenosis
  • 31.
    When a waveformis obtained from an arterial site distal to a stenosis or occlusion, a single, forward velocity component is observed, with flow remaining above the zero baseline throughout the cardiac cycle. The peak systolic frequency is lower than normal, and the waveform becomes flat and rounded Distal to stenosis
  • 32.
    High resistance, lowvolume waveform Characteristic shoulder on systolic downstroke Due to pulse wave reflection from distal disease ShoulderShoulder
  • 33.
    Tardus: Longer risetime Parvus: Low PSV Severe stenosis or occlusion Tardus-Parvus waveformDamping waveform Increased systolic rise time Loss of pulsatility
  • 34.
    IF superficial femoralartery is patent, a PI less than 4 indicates a hemodynamically significant aortoiliac lesion, The PI of the normal common femoral artery has a mean value of 6.7. More distally, the PI increases to 8 in the popliteal and 14 in the PT artery A PI value greater than or equal to 4 is predictive of a hemodynamically normal aortoiliac segment.
  • 35.
      Aorto-iliac: 25%  Femoro-popliteal: 65% Infra-popliteal: 10%
  • 36.
    Proximal: 2 cmproximal to stenosis At stenosis : Same Doppler angle if possible
  • 37.
  • 38.
    SFA: PSV of A69 cm/sec PSV of B 349 cm/sec B / A 349 / 69 = 5 > 80% diameter stenosis
  • 39.
    2 severe stenosesdemonstrated in SFA Areas of color flow disturbance & aliasing (arrows)
  • 40.
    Drop-out of colorflow signal in parts of lumen
  • 41.
    Occlusion in CIA Reversedflow in IIA (blue) to supply flow to EIA (red)
  • 42.
    Ultrasound cannot providereliable imaging if there are poor acoustic windows (eg, bowel gas attenuation, diffuse vascular calcification, or metallic stents) or poor intrinsic echogenicity of the tissues. Duplex scanning is time-consuming and inconvenient post-operatively – when the region of interest is obscured by dressings – and removing these can involve infection risk.
  • 43.
    DSA is thegold-standard for diagnostic imaging of PAD patients . It enables large field-of view (FOV) imaging with the highest possible in-plane resolution compared to other modalities. Drawbacks - catheterization, nephrotoxic contrast, exposure to high doses of ionizing radiation. The procedure is associated with major risks such as allergic reactions, infections at the site of vascular access, iatrogenic arteriovenous fistulas, hematomas, dissections. Digital subtraction angiography (DSA)
  • 44.
    Complications are reportedto occur in 0.17-7% of procedures, depending on the arterial viability, the size of the catheter, the experience of the clinician, and the location of the vascular access. Given the invasiveness of the procedure, its applications is now limited to patients who require a surgical or percutaneous procedure for therapeutic purposes •DSA is the "gold standard" to diagnose, and often to treat vascular disease. It involves getting detailed x-ray images of the arteries while injecting dye directly into the arteries. For patients with poor kidney function, a non-toxic gas carbon dioxide can be used in place of IV dye. Blockages can often be opened minimally invasively during an angiogram.
  • 45.
  • 46.
    A) A catheterhas been passed from the right common femoral artery and into the abdominal aorta during a digital subtraction angiogram. Contrast injection through the catheter reveals minor atherosclerotic wall abnormalities in the infrarenal aorta and the left common femoral artery B) Lower limb images reveal diffuse atherosclerotic disease of the superfi cial femoral and popliteal arteries of both sides, with a focal area of significant stenosis in the right popliteal artery.
  • 47.
    CT Angiography (CTA) CTAenables visualization of the entire peripheral vascular tree and offers information about lesion length, diameter, and morphology, as well as degree of calcification, and status of distal runoff vessels. A number of studies have compared CTA to the gold-standard DSA, showing comparable diagnostic accuracy and high confidence in clinical decision-making solely based on CTA .
  • 48.
    CTA offers evaluationof plaque, calcification, and vascular wall, while DSA depicts only arterial lumen. Technical limitations ---- inability to characterize calcified lesions, particularly in smaller vessels, due to beam-hardening artifacts. Drawbacks – radiation doze nephrotoxicity of contrast, which is contraindicated in patients with decreased renal function and renal insufficiency.
  • 49.
    CTA image ofthe iliofemoral arteries. Severe, focal stenosis (arrow) is present in the right mid-to-distal superficial femoral artery
  • 50.
    MR Angiography (MRA) CE-MRAis similar in set-up and diagnostic quality to CTA. CE-MRA methods rely on an injection of contrast material, which alters the magnetic properties of blood. Peripheral MRA is routinely performed with gadolinium (Gd)-based contrast agents . As vascular contrast is relatively independent of flow-dynamics, CE-MRA can be used for large field-of-view (FOV) imaging.
  • 51.
    For assessment ofhemodynamically significant disease Gd-MRA has reported sensitivities of 89-99.5% and specificities of 95-99% compared to DSA. Advantages of CE-MRA over CTA === no ionizing radiation ability to depict lumen of calcified vessels. Limitations == cost, scan time metal artifacts from stents and surgical clips. Association between nephrogenic systemic fibrosis and gadolinium contrast has limited the applicability of CE-MRA in kidney disease patients.
  • 52.
    Among the imagingmodalities used in PAD evaluation, usg has no contraindications for patient with renal insufficiency. Ultrasonography alone is inadequate for planning of surgical procedures because it does not provide accurate visualization of the entire peripheral vascular tree. Among the remaining modalities, both DSA and CTA, given their exposure to nephrotoxic contrast material and ionizing radiation, are unsafe for kidney disease patients. Recent association between nephrogenic systemic fibrosis and gadolinium contrast has challenged the safety of CE- MRA as well
  • 53.
  • 54.
    Symptomatic iliac arteryocclusive disease, diagnosed with gadolinium-enhanced MR angiography. (a) Coronal MIP image from a gadolinium-enhanced 3D MR angiographic study performed with administration of gadopentetate dimeglumine demonstrates bilateral severe proximal iliac artery stenoses, with the right greater thanthe left (arrows). (b) The next anatomic station was imaged 10 minutes after the preceding study with a second dose of gadopentetate Dimeglumine by using a slightly faster sequence. There is
  • 55.
    Unlike DU, MRA allowssimultaneous angiographic as well as anatomical volume acquisition of the whole body in seconds whilst maintaining high spatial resolution. This allows both luminal and extra-luminal pathology to be shown simultaneously, although magnetic resonance imaging is poorer for bony anatomy than computed tomography
  • 56.
    Like DSA, contrastenhanced magnetic resonance imaging is sensitive to patient motion artefacts. If there is patient motion between the mask acquisition and postcontrast acquisition, there will be image degradation following subtraction. Magnetic resonance cannot image calcification or steel stents; causes susceptibility artefacts recognizable as signal voids in the image. Metallic structures within the vessel lumen or adjacent to the vessel may cause magnetic susceptibility artefacts that obscure the vessel lumen leading to a false diagnosis of a stenosis or obstruction.
  • 57.
    Non-Contrast Magnetic Resonance Techniquesfor Peripheral Angiography In recent years there has been a renewed interest in unenhanced techniques, determined by two major factors. (1) improvements in MRI hardware and software have reduced acquisition times and made non-contrast imaging clinically practical (2) concerns about NSF in advanced renal disease patients
  • 58.
    Non-contrast MRA techniquesrely on flow-induced changes in the longitudinal or transverse magnetization of blood to obtain contrast between the vasculature and stationary background without administration of exogenous contrast material. Four major approaches for artery-background contrast generation exist: (1) Time-of-flight techniques (TOF) rely on differences in exposure to radiofrequency excitation between stationary tissue within the volume of interest and blood protons flowing into the imaging slab from outside the FOV.
  • 59.
    (2) Phase-contrast MRArelays on measurable velocity- induced changes in the phase of the blood signal (3) ECG-triggered subtraction techniques relay on the difference in arterial flow velocity between systole and diastole; either gradient echo or fast spin-echo read out can be used (4) Flow-independent angiography uses an acquisition that naturally provides bright blood signal weighting, combined with inversion-recovery and T2 preparation to null the signal of background tissues.
  • 60.
    Currently, the MRangiographic approach to the tibial vessels is dominated by the use of TOF techniques This flow-dependent strategy circumvents the challenge of achieving a sufficient concentration of contrast medium to effectively demonstrate the distal arterial Vessels. At present, TOF imaging offers the surgeon sufficient information to make the primary surgical decisions
  • 61.
    Overestimation of segmentalocclusions with TOF imaging. (a) Coronal MIP image obtained with TOF imaging demonstrates bilateral iliac artery occlusions, with right greater than left. (b) MIP image from a gd-enhanced 3D MR angiogram shows a shorter length of each occlusion compared with a. The depiction of the right hypogastric artery which was not seen with TOF imaging. Suppression of thesignal from retrograde flow is a major limitation of TOF strategies designed to eliminate venous signal.
  • 62.
    Vascular calcifications ina patient with diabetes mellitus. A, Coronal thin section maximum intensity projection (MIP) of a computed tomography angiography of the tibial peroneal runoff vessels demonstrating how dense calcifications in this patient population obscures analysis of the lumen. B, Contrast-enhanced magnetic resonance angiography is insensitive to vascular calcification as well as bone, simplifying image interpretation as demonstrated in this full-volume MIP from the same patient as in A.
  • 64.
    – directed towardprevention of vessel occlusion  use of vasodilators Surgical intervention – in advanced disease – ischemic changes and pain severely impairs activity  Embolectomy › removal of a blood clot, done when large arteries are obstructed  Endarterectomy › is removal of a blood clot and stripping of atherosclerotic plaque along with the inner arterial wall.  Arterial by-pass surgery › an obstructed arterial segment may be bypassed by using a prosthetic material (Teflon) or the pt’s. own artery or vein (saphenous vein)
  • 65.
    Primary treatment strategyaccording TASC severity TASC A - endovascular therapy TASC B - endovascular therapy TASC C - surgical therapy (if patient is able to be operated, otherwise endovascular therapy) TASC D - surgical therapy
  • 66.
  • 70.
     Percutaneous TransluminalAngioplasty › The balloon tip of the catheter is inflated to provide compression of the plaque  Amputation › with advanced atherosclerosis & gangrene of extremities › toes are the most often amputated part of the body
  • 71.
    FA lumen filledwith hypoechoic thrombus or embolus Good delineation of vessel wall without signs of plaque Normal flow in adjacent FV .
  • 72.
    Aneurysm Diameter increase >50% of normal expected diameter Ectasia Diameter increase < 50% of normal expected diameter Considerable variability in normal diameter of arteries Depends on physical size, sex, & age Considerable variability in normal diameter of arteries Depends on physical size, sex, & age .
  • 73.
  • 74.
  • 75.
    Sonography is therecommended non- invasive technique for the postoperative monitoring of bypass graft patency Sonography is the recommended non- invasive technique for the postoperative monitoring of bypass graft patency
  • 76.
     Synthetic graft PTFE*Above knee  Autologous vein * PTFE: Polytetrafluoroethylene
  • 77.
    Aorto-bi-femoral graft Femoral-to-femoralartery bypass graft Peripheral arterial bypass graft – 1
  • 78.
  • 79.
    Composite PTFE &vein graft Slightly dilated area corresponding to valve site In situ vein graft
  • 80.
    Hyperemic flow oftenseen in early postoperative period Hyperemic monopahasic flow Pulsatile flow Over time, flow normally assumes a pulsatile flow
  • 81.
    Average PSV from 3– 4 sites without stenosis Graft flow velocity Normal PSV: 45 – 180 cm/s
  • 82.

Editor's Notes

  • #14 Dysesthesia:
  • #23 Care must be taken when interpreting ABPI measurements from diabetic patients as the arterial walls of the calf arteries are often calcified and rigid. This means that the vessels may not collapse under the pressure of the cuff as it is inflated, leading to falsely elevated recordings.
  • #29 Differential diagnosis Collateral function of a vessel Exercise-induced hyperemia - Peripheral inflammation
  • #36 approximate frequency for predominant disease at each level is: ● aortoiliac 25 per cent ● femoropopliteal 65 per cent ● infrapopliteal 10 per cent (more frequent in diabetics).
  • #40 Poststenotic Doppler spectrum recorded behind the most proximal obstruction is also influenced by flow alterations caused by lesions distal to the sampling site. In patients with sequential stenoses or occlusions, the usual stenosis criteria may thus lead to misinterpretation. In grading a second stenosis, the examiner has to take into account the hemodynamic changes (change in pulsatility and pressure drop) produced by the preceding stenosis: the postocclusive decrease in velocity after the first stenosis will result in a lower absolute PSV in the second stenosis (and the PSV of 180 cm/s proposed as a criterion for isolated stenosis does not apply insequential stenoses). Therefore, only the criterion of a 100% increase in PSV can be used to classify a sequential stenosis as hemodynamically significant.
  • #73 Johnston K W, Rutherford R B, Tilson M D, et al 1991 Suggested standards for reporting on arterial aneurysms. Subcommittee on Reporting Standards for Arterial Aneurysms, Ad Hoc Committee on Reporting Standards, Society for Vascular Surgery and North American Chapter, International Society for Cardiovascular Surgery. Journal of Vascular Surgery 13(3):452 – 458.
  • #74 TRTrue lumen IIntima MMedia AAdventia FL False lumen
  • #81 New grafts may demonstrate a hyperemic monophasic flow profile because of sustained peripheral vasodilation, which can be due to a combination of the previous ischemia and healing tissue. Over time, the flow pattern should become pulsatile, and biphasic or triphasic waveforms are usually recorded.