Clinical Application of Pulsatility Index: Review Article
Clinical Application of Pulsatility Index: Review Article
Clinical Application of Pulsatility Index: Review Article
www.journals.viamedica.pl/medical_research_journal 201
MEDICAL RESEARCH JOURNAL 2020. vol. 5. no. 3
202 www.journals.viamedica.pl/medical_research_journal
Melanie Wielicka et al., Pulsatility index
sively summarize its clinical applications. Thus, we Pulsatility index in atherosclerosis and arterial
would like to discuss the value of pulsatility index in the stenosis
macrovascular examination.
Several studies report a relationship between pul-
satility and atherosclerotic disease. Pulsatility index
Clinical applications of PI has been studied as an additional parameter when
assessing arterial wall shear stress, an important
Pulsatility index in hypertension and heart disease predictor of cardiovascular risk and atherosclerosis
development. Avrahami et al have studied pulsating
Many available reports discuss the association flow waveforms in a straight, rigid tube, with and without
between the loss of arterial elasticity and hypertension. flow reversals. Their results had indicated that adding
A study by Clime et al explains that increased blood PI to the already widely used average flow rate and
pressure values are associated with an increase in inti- heart rate measurements improve diagnostic evaluation
mal-media thickness, lumen enlargement and increased [20]. Jotoku et al. have shown a significant association
stiffness of proximal elastic arteries [6]. Conversely, between pulsatility index of the common carotid artery
Mitchell discusses several publications that have shown with cardiovascular risk factors, namely homocysteine
that the arterial stiffness precedes and strongly contrib- and monocyte levels. Both of the latter parameters
utes to the development of hypertension [9]. have been shown to be related to coronary plaque
In hypertensive patients, the pulsatility index can development and progression in acute myocardial
be used as a predictor of complications and help infarction [21].
assess chronicity of disease. Cho et al measured flow As per Poiseuille’s Law, a decrease in vascular diam-
velocities and Gosling Index of the middle cerebral and eter, such as in the case of arterial stenosis, leads to an
internal carotid arteries in 94 hypertensive patients. They increase in vascular resistance [22]. An increase in PI
demonstrated a significant decrease in flow velocities, is a reliable marker of distal resistance in the examined
and an increase in the Gosling index in patients who blood vessel [11], which is why it can be useful in as-
had hypertension for over five years. These differences sessing the distal parts of examined vessels that are not
were not present in patients with a shorter duration of as easily accessible with ultrasound techniques. Thus,
the disease [14]. the pulsatility index as a measure of vascular resistance
PI has also been studied in patients with renovas- has been utilized in assessing arterial narrowing and
cular hypertension, and hypertension associated with efficacy of treatment in carotid artery stenosis. Heyer
renal failure. A report by Bardelli et al discusses the et al [23] studied PI of the middle cerebral artery in
possible use of the pulsatility index of renal arteries as patients with carotid artery stenosis and its correla-
an indicator of bilateral renal artery stenosis in hyper- tion with cerebral blood flow and cognitive function
tensive patients. They were able to correctly diagnose post carotid endarterectomy. The authors explained
renovascular hypertension in 84% of patients, while the that those patients frequently have reduced cerebral
presence of renal artery stenosis was established in 94% vascular resistance, likely through autoregulation, to
of patients [16]. Renal artery PI and resistive index have compensate for decreased cerebral blood flow, with PI
also been demonstrated to be associated with renal values in symptomatic patients typically documented
function parameters, such as creatinine clearance, in to be < 1.0. They found that symptomatic patients with
patients with renal failure and hypertension [17]. Addi- a low baseline PI (=< 0.80) are likely to have increased
tionally, Okuma et al studied intrarenal PI and resistive cerebral blood flow and improved cognitive function
index in patients with hypertension and showed that even 1 day after carotid endarterectomy.
they are positively correlated with carotid intima-media Wada et al [24] investigated whether carotid ultra-
thickness, suggesting that those measurements could sonography indices could help detect the progression
be used in the evaluation of arterial stiffness in hyper- of arterial stenosis in patients with vertebral artery (VA)
tensive patients [18]. dissection. In patients admitted with intracranial VA
In a recently published study from 2019, Sasaki dissection, an MR angiography (MRA) was performed at
et al have shown that common carotid artery PI, as admission and after a median of 20 days, while the base-
well as resistance index measurements, are associ- line peak systolic velocity, end-diastolic velocity, mean
ated with the log NT-pro-BNP levels in hypertensive velocity and pulsatility index were measured at admis-
patients, suggesting that PI could be a useful marker sion and followed up after a median of 22 days. A follow
of hemodynamic stress on the left ventricle, while up to baseline ratio was then calculated. The PI ratio
mean intima-media thickness, number of plaques was significantly higher in patients with stenosis pro-
and plaque score had no association with log gression, while there were no significant differences in
NT-proBNP [19]. the other measured parameters. The authors concluded
www.journals.viamedica.pl/medical_research_journal 203
MEDICAL RESEARCH JOURNAL 2020. vol. 5. no. 3
Figure 2. Extra-cranial Doppler Duplex examination of vertebral artery. A — normal flow pulsatility; B — increased
pulsatility due to distal occlusion with preserved collateralization by Posterior Inferior Cerebellar Artery; C — increased
pulsatility due to distal occlusion without preserved collateralization by Posterior Inferior Cerebellar Artery. AC — angle
correction [The exam performed at the Laboratory of Neurosonology of the Department of Neurology, Collegium
Medicum in Bydgoszcz, Nicolaus Copernicus University in Toruń, head of the clinic dr. hab. G. Kozera, ESAOTE MyLab
Class C apparatus with a 5.5 MHz (A) linear probe and in the Laboratory of Neurosonology of the Clinic of Neurology,
Medical University of Gdańsk, head of the clinic prof. W. M. Nyka, GE Vivid I device with 5.5 MHz linear probe (B–C)]
that PI might be a useful index in the detection of arterial vessels and that PI and RI are reliable in diagnosing
stenosis progression. Thus, an increase in PI may be cerebrovascular malformations [27].
currently used as an ultrasonographic marker of distal Kaspera et al. studied the impact of treatment on
stenosis or occlusion and help to predict its site (Fig. 2). hemodynamic parameters of AVMs using color-coded
PI has also been used in patients with age-related doppler sonography. They assessed mean flow velocity,
aortic stenosis. Cay et al investigated the association pulsatility index and vasomotor reactivity in the major
between ascending aortic pressure-derived indices and cerebral vessels in 46 adult patients who were all diag-
hemodynamic characteristics of calcific aortic stenosis nosed with AVMs. These parameters were recorded at
(AS) [25]. They measured fractional pulse pressure admission, within 24 hours after the first embolization or
(FFP) and pulsatility index in the ascending aorta in surgical resection, and before the second embolization.
a group of patients with aortic stenosis and healthy The authors found a decrease in mean flow velocity and
controls. Both values were significantly higher in the AS an increase in PI in the embolized feeding vessels [28].
group. The authors suggested future studies could po-
tentially evaluate the prognostic value of both FFP and Pulsatility index in diabetes
PI in determining the severity of calcific aortic stenosis.
According to the CDC statistics, there were in total of
Pulsatility index in vascular malformations 26.9 million diagnosed cases of diabetes in the United
States in 2018 alone, with only 5.2% of these cases ac-
In neurosurgery, PI is helpful in the evaluation of counted for by type 1 diabetes [29]. Long-standing hy-
cerebral arteriovenous malformations (AVMs). The feed- perglycemia in diabetic patients is known to damage the
ing arterioles in AVMs empty directly into a vein with no vascular endothelium, and correlates with an increase
capillary network in between to increase resistance. This in vascular stiffness [30], increasing pulsations. The
has been associated with high-flow and low resistance increased pulsations resulting from the stiffness of
within the ACMs, with a decrease in PI values [26]. large vessels are also believed to affect the capillary
Burkhardt et al. have analyzed hemodynamic profiles, networks, resulting in microvascular complications [31].
measured flow velocities, resistance index and pulsatil- Thus, several studies have shown a possible application
ity index of feeding and draining arteries in 32 patients for the pulsatility index in examining the larger blood
with AVMs with the use of intraoperative micro-Doppler vessels to predict and prevent microvascular compli-
(IOMD). They concluded that IOMD is a safe and useful cations in diabetic patients, especially in the renal and
tool which helps in eliminating only the necessary blood cerebral circulation.
204 www.journals.viamedica.pl/medical_research_journal
Melanie Wielicka et al., Pulsatility index
In a study from 2006, pulsatility index at the internal the presence of asymptomatic brain injury (white matter
carotid artery was used to indicate presence of mi- lesions, WML) may be related to higher PI in the pres-
croangiopathy by showing its strong correlation with ence of additional confounders, such as type 2 diabetes
microalbuminuria in type 2 diabetic patients [32]. A dif- and ACE inhibitor or statin use [37].
ferent, more recent study from 2018, has determined the The decline in peripheral vascular function is also an
relationship between renal resistivity index, pulsatility important complication of diabetes. In 2005, Janssen
index and renal function parameters, namely urinary suggested pulsatility index as a non-invasive method
albumin secretion rate, serum creatinine levels and of evaluation of critical limb ischemia in patients with
eGFR (estimated glomerular filtration rate). The positive diabetic neuropathy. This study even compares PI to
correlation between PI, albuminuria and serum creati- ankle-brachial doppler index and the systolic ankle
nine, combined with a negative correlation with eGFR, pressure, and shows that it is superior to the other
suggest that PI may be a useful parameter in predicting methods when assessing critical limb ischemia in this
renal dysfunction in type 2 diabetic patients [13]. group of patients [38]. In a study by Zou et al, the
Lee at al. have shown that pulsatility index at the authors explored the clinical value of ultrasound exam-
middle cerebral artery and at the internal carotid artery ination combined with a warm bath in the assessment
was significantly higher in patients with microvascular of the microcirculation in diabetic patients. Several
complications such as retinopathy, nephropathy and Doppler parameters were used, including pulsatility
neuropathy than those with no complications and and resistivity indices at the dorsalis pedis artery and
healthy controls. Their study population consisted of plantar digital artery. They suggested that color dop-
56 types 2 diabetic patients, with a mean age of 59, pler combined with a warm bath test could potentially
and 70 age-and gender-matched controls [33]. Agha be used when assessing the differences in reactivity
et al have measured pulsatility index along with flow of distal limb microvasculature in patients with type
velocity at the middle cerebral, basilar and intracranial 2 diabetes [13].
portion of the internal carotid artery in a large sample of Additionally, the pulsatility index has been used to
141 of diabetic patients and 131 age and sex-matched help assess the effects of certain therapies in diabetic
controls. Their results have demonstrated a statistical- patients. A study from 2016 used PI to analyze the
ly significant difference between these values when effect of Naoxitong Capsules on vascular remodelling
they compared patients with diabetes to healthy con- of carotid artery in type 2 diabetic patients [39]. In
trols. When dividing the diabetic group into patients another report by Park et al. the effect of pioglitazone
with or without complications, they were also able to on the pulsatility index of cerebral arteries and carotid
demonstrate significant differences between those two intima thickness in type 2 diabetic patients was studied.
sub-groups. They had concluded that arterial pulsatility The study group involved 40 types 2 diabetic patients,
index can be used as an indicator of the presence of divided into two groups: one treated with pioglitazone
cerebral microangiopathy in type 2 diabetic patients and one treated with gliclazide. Pulsatility index was
[34]. A different study on cerebrovascular pulsatility in calculated for each group based on transcranial Dop-
diabetes investigated the relationship between insulin pler examination and was found to be significantly
resistance and pulsatility index in diabetic patients by decreased in the pioglitazone treated group. Through
measuring the PI at middle cerebral artery [35]. The obtaining the PI measurements, the authors were able
authors found that pulsatility index was significantly to conclude that pioglitazone improved cerebrovascular
higher in diabetic patients when compared to healthy resistance in type 2 diabetic patients [40].
controls, and additionally, was also higher in patients
who had insulin resistance confirmed with a short Pulsatility index in children
insulin tolerance test, than in patients with diabetes
alone. However, it is important to note that the age and In healthy subjects, PI is an age-dependent param-
duration of diabetes independently contributed to the eter. This fact was described by Schoning et al [41, 42]
changes in PI between the subgroups. Kozera et al. in their studies applying ultrasound examination of PI for
studied the presence of cerebral and skin angiopathy in common carotid artery in healthy children, adolescents
adult patients with type 1 diabetes mellitus. In a group and adults. They showed that PI changes from value
of adult patients with type 1 diabetes mellitus, authors 1.73 ± 0.31 for children under 10 years of age through
found no significant association between cerebral and 1.97 ± 0.42 in children and adolescents over 10 years of
skin microvasculature function despite the simultane- age [41] to 1.72 ± 0.5 for adults [41, 42]. The significant
ous presence of cerebral microangiopathy reflected differences of PI between groups were shown. It is worth
by increased PI of the middle cerebral artery and skin noticing that according to Shoning et al., pulsatility
microangiopathy (reflected in by increased COVERAGE index at common carotid in adults artery significantly
of skin capillaries)[36]. Kozera et al. also showed that decreases with age (r = -0,52, p = 0.001) [42].
www.journals.viamedica.pl/medical_research_journal 205
MEDICAL RESEARCH JOURNAL 2020. vol. 5. no. 3
Pulsatility index, being a fast, simple and non-in- disease. The thyroid arteries, although significantly
vasive test that does not require a lot of cooperation, smaller than the main pulsatile arteries of the cardio-
has many applications in the pediatric population. For vascular system, such as the aorta, the carotid arteries
instance, it has been used to evaluate renal vascula- or the renal arteries, still play a significant role in diag-
ture in type 1 diabetic children. A study from 2010 has nostics. Thus, several studies have investigated the use
investigated renal resistive index as well as pulsatility of measuring the pulsatility index in thyroid vessels.
index in a large sample of 100 diabetic children, aged A study from 2018 evaluated a large group of
13.4 ± 2.9 years, with an average diabetes duration 208 patients with a mean age of 37.7 years to establish
7.2 ± 2.5 years, as well as in 30 healthy controls. Both the mean values in euthyroid adults of pulsatility index,
pulsatility Index (mean PI left/right in diabetic patients along with RI and PSV, of the superior thyroid arteries
1.15 ± 0.2, mean PI left/right in healthy controls in euthyroid adults. The mean PI obtained in this study
1.0 ± 0.1, p = 0.04) and Resistivity Index (mean RI was 0.93 ± 0.31, and no significant differences were
left/right in diabetic children 0.72 ± 0.1, mean RI found between males and females [47].
left/right in healthy controls 0.6 ± 0.045, p = 0.001) A case-control study from 2015 investigated carotid
were significantly higher in children with type 1 diabetes, artery hemodynamics and cardiovascular risk factors in
particularly in those who had additionally been diag- 31 women with Hashimoto thyroiditis on levothyroxine
nosed with insulin resistance syndrome, hypertension treatment and 26 euthyroid women with Hashimoto
or obesity. The authors concluded that these doppler thyroiditis without levothyroxine treatment. They mea-
parameters should be added to the routine workup in sured carotid intima-media thickness, carotid extra-me-
diabetic children, especially with these additional risk dia thickness and pulsatility indexes in the common
factors, as they could potentially help diagnose diabetic carotid artery and internal carotid artery. PI CCA and
nephropathy before the appearance of albuminuria. PI ICA were both increased in the study group when
This study also shows that the results obtained through compared to the controls (p = 0.02 and p = 0.047),
PI measurements may also be supported by other while CIMT and CEMT were similar in both groups. The
parameters - in this specific case, resistivity index [43]. authors concluded, that it was the hormonal imbalance
Sawires et al. have also suggested PI as one of the of hypothyroidism that influences arterial stiffness, and
Doppler markers of renal dysfunction in children. They not the autoimmune disease process itself, that causes
have shown a significant difference in PI (p = 0.02), arterial stiffness [48]. In a more recent study by Kalantari
amongst other tested parameters, when comparing [49], he investigated the use of color doppler and gray
a group of 42 children with chronic kidney disease scale ultrasound on predicting thyroid nodule malignan-
(1.05 ± 0.36) with 42 healthy controls (0.89 ± 0.23) [44]. cy. All of the 63 participants had a thyroid ultrasound
Additionally, PI in children appears to have sever- done, which was followed by fine-needle aspiration and
al applications in Pediatric Neurology. A study from surgery. Out of the doppler parameters obtained in this
2015 suggests that PI could be used as a simple, study, pulsatility index was the most predictive factor
non-invasive method of assessing raised intracranial of thyroid malignancy, with a positive predictive value
pressure in children who are at risk but do not meet all (PPV) of 62% and a negative predictive value (NPV) of
the criteria for invasive monitoring. The PI measured 100%. The author concluded that a combination of the
at the middle cerebral artery had good specificity and presence of calcifications, a resistive index at or above
sensitivity in predicting increased intracranial pressure 0.715 and a PI at or above 0.945 was strongly diagnostic
in children with early acute brain injury [45]. of malignancy (PPV = 66.6%, NPV 98.4%).
Pulsatility index and thyroid disease Pulsatility index as a marker of brain edema
Hypothyroidism, which affects between 4–10 % of Published reports indicate that increased flow
the population, is known to have many negative effects pulsatility in main cerebral arteries may reflect raised
on the cardiovascular system. It is associated with im- intracranial pressure (ICP) in brain edema. Asil et al
paired relaxation of the vascular smooth muscle and [50] showed that in patients with ICP progression in
release of nitric oxide, arterial stiffness and increased malignant middle cerebral artery (MCA) infarction the
vascular resistance. It also impacts the renal-angio- pulsatility indices of MCA were higher on the third hospi-
tensin-aldosterone system, as hepatic renin synthesis tal day than on the first day, and PI were correlated with
is stimulated by triiodothyronine. Additionally, it has the midline shift measured on the third day after stroke.
a strong effect on lipid metabolism, resulting in elevated They also showed worse prognoses in patients with
total cholesterol, LDL and apolipoprotein B [46]. PI > 1.5 than PI < 1.5. Bor-Seng-Shu [51] reported that
Ultrasonography of the thyroid gland is one of the PI values decrease significantly after decompressive
most common tests performed in diagnosing thyroid craniectomy. On the other hand, some authors indicate,
206 www.journals.viamedica.pl/medical_research_journal
Melanie Wielicka et al., Pulsatility index
that PI-based methods can not predict ICP reliably, index (PI) is an easy to obtain parameter with a broad
as some studies show poor or inexistent correlations range of both, research and clinical applications. It has
between both parameters. Nevertheless, flow spectra been widely used in the assessment of macrocirculation
analysis with the use of Transcranial Doppler is applied in highly prevalent chronic medical conditions, such
as a supportive method in the procedure of the brain as hypertension, both type 1 and type 2 diabetes and
death confirmation [50, 52] (Fig. 3, Tab. 1). thyroid disorders. For instance, in diabetic patients, it
has been found to be of great value in prediction and
early diagnosis of microvascular complications.
Conclusion Amongst the cited articles, PI has mainly been mea-
sured at carotid arteries and middle cerebral arteries,
Based on our extensive review of the literature and but also at renal arteries, peripheral limb vasculature or
the gathered information, we conclude that pulsatility thyroid vessels. Because it is non-invasive and requires
Figure 3. Transcranial Doppler examination of Middle Cerebral Artery. Left picture — normal flow with low pulsatility (PI
0,62); right picture — increased pulsatility (PI 1,18) due to raised intracranial pressure (Exam performed Laboratory of
Neurosonology, Department of Neurology, Collegium Medicum in Bydgoszcz, Nicolaus Copernicus University in Toruń,
head of the clinic dr. hab. G. Kozera, using a Viasys Companion III camera with a PW 2MHz probe
Æ
www.journals.viamedica.pl/medical_research_journal 207
MEDICAL RESEARCH JOURNAL 2020. vol. 5. no. 3
Agha [34]/2014 141 diabetic patients and 131 sex and age- PI and flow velocity at middle cerebral,
matched controls basilar and intracranial portion of the
internal carotid artery
Park [35]/2008 90 patients with stroke-free type 2 diabetes PI in middle cerebral artery
and 45 healthy age- and sex-matched
controls
Kozera [36]/2019 51 patients with type 1 diabetes mellitus, PI in middle cerebral artery
with a median age of 37.5 years
Kozera [37]/2010 54 men with hypertension, all 60 years of PI in middle cerebral artery, Magnetic
age resonance imaging
Janssen [38]/2005 106 diabetic patients who presented with PI in ankle artery, digital subtraction
polyneuropathy arteriography, ankle-brachial Doppler
index, systolic ankle blood pressure
Zou [13] /2017 56 type 2 diabetic patients and 50 healthy PI and RI at the dorsalis pedis artery and
controls plantar digital artery, a warm bath test
Park [40]/2007 40 type 2 diabetic patients divided into two PI in middle cerebral artery and basilar
groups: one treated with pioglitazone, one artery, carotid intima-media thickness
treated with gliclazide
Pediatrics Schoning [41]/1998 48 adults, 94 healthy children and PI in common carotid artery
adolescents
Abd El Ghaffar 100 diabetic children, aged 13.4 ± 2.9, Renal PI and RI
[43]/2010 with an average diabetes duration 7.2 ±
2.5 years, and 30 healthy controls
Sawires [44]/2018 42 children with chronic kidney disease PI in renal arteries
and 42 healthy controls
O’Brian [45]/2020 36 children admitted to intensive care units PI in middle cerebral artery
with a diagnosis of severe traumatic brain
injury (GCS =< 8)
Thyroid disease Joish [47]/2018 208 patients with a mean age of 37.7 PI, RI and PSV of the superior thyroid artery
Owecki [48]/2015 31 women with Hashimoto thyroiditis on PI in common carotid artery and PI in
levothyroxine treatment and 26 euthyroid internal carotid artery
women with Hashimoto thyroiditis without
levothyroxine treatment.
Kalantari [49] /2018 63 patients with thyroid nodules. PI and RI at thyroid nodules
Brain edema Asil [50]/2003 18 patients with first-ever strokes and large PI in middle cerebral artery
MCA (middle cerebral artery) infarction
Bor-Sheng-Shu 19 patients presenting with traumatic brain PI in transcranial ultrasonography
[51]/2013 swelling
208 www.journals.viamedica.pl/medical_research_journal
Melanie Wielicka et al., Pulsatility index
little cooperation, it has also been widely used in pedia angiography. Interventional Neuroradiology. 2017; 23(4): 357–361, doi:
10.1177/1591019917701100.
tric populations. In pediatric patients with diabetes, it 11. Kassab MY, Majid A, Farooq MU, et al. Transcranial Doppler:
has been shown to aid with diagnoses of renal damage An Introduction for Primary Care Physicians. The Journal of the
American Board of Family Medicine. 2007; 20(1): 65–71, doi:
prior to the development of microalbuminuria. In the 10.3122/jabfm.2007.01.060128.
emergency room setting, it has been suggested as 12. Soyoye DO, Dawha SD, Ayoola OO, et al. Relationship between Renal
a useful tool in assessing raised intracranial pressure in Doppler Indices and Biochemical indices of Renal Function in Type 2
Diabetes Mellitus. West Afr J Med. 2018; 35(3): 189–194.
patients with acute head trauma [45]. It may also serve 13. Zou C, Jiao Y, Li X, et al. Differences between healthy adults and pa-
as an indirect sign of distal pathology in the assessed tients with type 2 diabetes mellitus in reactivity of toe microcirculation
by ultrasound combined with a warm bath test. Medicine. 2017; 96(22):
vascular bed in case of stenosis (where the PI value in- e7035, doi: 10.1097/md.0000000000007035.
creases) and widening (where the PI value decreases). 14. Cho S, Sohn Y, Kim G, et al. Blood flow velocity changes in the middle
cerebral artery as an index of the chronicity of hypertension. Journal of
Thus, it may indicate the necessity of further evaluation the Neurological Sciences. 1997; 150(1): 77–80, doi: 10.1016/s0022-
of distal segments that are not easily accessible with -510x(97)05391-4.
ultrasound techniques. 15. Mitchell G. Aortic stiffness, pressure and flow pulsatility, and target or-
gan damage. Journal of Applied Physiology. 2018; 125(6): 1871–1880,
PI has the potential to be used in the assessment doi: 10.1152/japplphysiol.00108.2018.
of disease progression and treatment efficacy. It has 16. Bardelli M, Jensen G, Volkmann R, et al. Non-invasive ultrasound
assessment of renal artery stenosis by means of the Gosling pul-
been suggested to have value in assessing the severity satility index. Journal of Hypertension. 1992; 10(9): 985???990, doi:
of calcific aortic stenosis [25], while in hypertensive 10.1097/00004872-199209000-00011.
patients it has been demonstrated to correlate with 17. Petersen LJ, Petersen JR, Ladefoged SD, et al. The pulsatility index and
the resistive index in renal arteries in patients with hypertension and
disease duration [14]. It was also used to determine chronic renal failure. Nephrol Dial Transplant. 1995; 10(11): 2060–2064.
the effect of pioglitazone therapy on cerebrovascular 18. Okura T. Intrarenal and carotid hemodynamics in patients with essential
hypertension. American Journal of Hypertension. 2004; 17(3): 240–244,
resistance in diabetic patients [40].With this article, we doi: 10.1016/j.amjhyper.2003.10.005.
would like to encourage wider use of pulsatility index, 19. Sasaki N, Yamamoto H, Ozono R, et al. Association of Common Carotid
and demonstrate the clinical areas in which there is Artery Measurements with N-terminal Pro B-type Natriuretic Peptide
in Elderly Participants. Internal Medicine. 2020; 59(7): 917–925, doi:
potential for more research with the use of this doppler 10.2169/internalmedicine.3780-19.
parameter. PI is non-invasive, inexpensive and, when 20. Avrahami I, Kersh D, Liberzon A. Pulsatility Index as a Diagnostic
Parameter of Reciprocating Wall Shear Stress Parameters in Physio-
used skillfully, may be extremely helpful in diagnosing logical Pulsating Waveforms. PLOS ONE. 2016; 11(11): e0166426,
a variety of complex vascular pathologies. doi: 10.1371/journal.pone.0166426.
21. Jotoku M, Okura T, Miyoshi Ki, et al. Carotid hemodynamics is associa-
ted with monocyte count determined by serum homocysteine level in
Statement of competing interests: The authors de- patients with essential hypertension. Clinical and Experimental Hyper-
clared no potential conflicts of interest with respect to the tension. 2014; 37(5): 358–363, doi: 10.3109/10641963.2014.972563.
22. Norouzpour A, Hooshyar Z, Mehdizadeh A. Autoregulation of blood
research, authorship, and/or publication of this article. flow: Vessel diameter changes in response to different temperatures. J
Biomed Phys Eng. 2013; 3(2): 63–6.
23. Heyer E, Mergeche J, Connolly E. Middle cerebral artery pulsatility
index and cognitive improvement after carotid endarterectomy
References for symptomatic stenosis. Journal of Neurosurgery. 2014; 120(1):
126–131, doi: 10.3171/2013.8.jns13931.
1. Tocci G, Sciarretta S, Volpe M. Development of heart failure in recent 24. Wada S, Koga M, Makita N, et al. Detection of Stenosis Progression
hypertension trials. Journal of Hypertension. 2008; 26(7): 1477–1486, in Intracranial Vertebral Artery Dissection Using Carotid Ultrasonogra-
doi: 10.1097/hjh.0b013e3282fe1d3d. phy. Journal of Stroke and Cerebrovascular Diseases. 2019; 28(8):
2. Roper NA, Bilous RW, Kelly WF, et al. Cause-Specific Mortality in a Po- 2201–2206, doi: 10.1016/j.jstrokecerebrovasdis.2019.04.033.
pulation With Diabetes: South Tees Diabetes Mortality Study. Diabetes 25. Cay S, Cagirci G, Atak R, et al. Ascending aortic pressure-
Care. 2002; 25(1): 43–48, doi: 10.2337/diacare.25.1.43. -derived indices are associated with the presence and severity
3. Bebu I, Schade D, Braffett B, et al. Risk Factors for First and Subsequ- of aortic stenosis. Blood Pressure. 2010; 19(1): 48–53, doi:
ent CVD Events in Type 1 Diabetes: The DCCT/EDIC Study. Diabetes 10.3109/08037050903312804.
Care. 2020; 43(4): 867–874, doi: 10.2337/dc19-2292. 26. Bartels E. Evaluation of Arteriovenous Malformations (AVMs) With
4. Einarson T, Acs A, Ludwig C, et al. Prevalence of cardiovascular Transcranial Color-Coded Duplex Sonography. Journal of Ultrasound in
disease in type 2 diabetes: a systematic literature review of scientific Medicine. 2005; 24(11): 1511–1517, doi: 10.7863/jum.2005.24.11.1511.
evidence from across the world in 2007–2017. Cardiovascular Diabe- 27. Burkhardt T, et al. Siasios G Schmidt NO Intraoperative Micro-Doppler
tology. 2018; 17(1), doi: 10.1186/s12933-018-0728-6. in Cerebral Arteriovenous Malformations. J Neurol Surg A Cent Eur
5. Graves L, Donaghue K. Management of diabetes complications in
Neurosurg. 2015; 76(6): 451–5.
youth. Therapeutic Advances in Endocrinology and Metabolism. 2019;
28. Kaspera W, Ładziński P, Larysz P, et al. Transcranial color-coded
10: 204201881986322, doi: 10.1177/2042018819863226.
Doppler assessment of cerebral arteriovenous malformation hemo-
6. Climie R, Gallo A, Picone D, et al. Measuring the Interaction Between
dynamics in patients treated surgically or with staged embolization.
the Macro- and Micro-Vasculature. Frontiers in Cardiovascular Medi-
cine. 2019; 6, doi: 10.3389/fcvm.2019.00169. Clinical Neurology and Neurosurgery. 2014; 116: 46–53, doi: 10.1016/j.
7. Gosling RD, King DH. Arterial assessment by Doppler-shift Ultrasound. clineuro.2013.11.001.
Proc R Soc Med. 1974; 67(6 Pt 1): 447–449. 29. Center for Disease Control and Prevention, section on type. https://
8. Barić D. Why pulsatility still matters: a review of current know- www.cdc.gov/diabetes/basics/type2.html.
ledge. Croatian Medical Journal. 2014; 55(6): 609–620, doi: 30. Dec-Gilowska M, Trojnar M, Makaruk B, et al. Circulating Endothelial
10.3325/cmj.2014.55.609. Microparticles and Aortic Stiffness in Patients with Type 2 Diabetes
9. Hussein A, Brunozzi D, Shakur S, et al. Cerebral Aneurysm Size and Mellitus. Medicina. 2019; 55(9): 596, doi: 10.3390/medicina55090596.
Distal Intracranial Hemodynamics: An Assessment of Flow and Pulsatility 31. Climie R, Picone D, Blackwood S, et al. Pulsatile interaction between
Index Using Quantitative Magnetic Resonance Angiography. Neurosur- the macro-vasculature and micro-vasculature: proof-of-concept
gery. 2017; 83(4): 660–665, doi: 10.1093/neuros/nyx441. among patients with type 2 diabetes. European Journal of Applied
10. Hussein A, Esfahani D, Linninger A, et al. Aneurysm size and the Physiology. 2018; 118(11): 2455–2463, doi: 10.1007/s00421-018-
Windkessel effect: An analysis of contrast intensity in digital subtraction 3972-2.
www.journals.viamedica.pl/medical_research_journal 209
MEDICAL RESEARCH JOURNAL 2020. vol. 5. no. 3
32. Fukuhara T, Hida K. Pulsatility Index at the Cervical Internal Carotid 43. Ghaffar SA, Kaffas KEl, Hegazy R, et al. Renal Doppler indices in diabe-
Artery as a Parameter of Microangiopathy in Patients With Type 2 tic children with insulin resistance syndrome. Pediatric Diabetes. 2010;
Diabetes. Journal of Ultrasound in Medicine. 2006; 25(5): 599–605, 11(7): 479–486, doi: 10.1111/j.1399-5448.2009.00628.x.
doi: 10.7863/jum.2006.25.5.599. 44. Sawires H, Salah D, Hashem R, et al. Renal ultrasound and Doppler
33. Lee K, Sohn Y, Baik J, et al. Arterial Pulsatility as an Index of Cerebral parameters as markers of renal function and histopathological damage
Microangiopathy in Diabetes. Stroke. 2000; 31(5): 1111–1115, doi: in children with chronic kidney disease. Nephrology. 2018; 23(12):
10.1161/01.str.31.5.1111. 1116–1124, doi: 10.1111/nep.13201.
34. Agha MS, Alboudi A. Arterial Pulsatility as an index of cerebral micro- 45. O’Brien N, Maa T, Reuter-Rice K. Noninvasive screening for intra-
angiopathy in diabetes type 2. 2014; 19(3): 198–203. cranial hypertension in children with acute, severe traumatic brain
35. Park J, Cho M, Lee K, et al. Cerebral arterial pulsatility and insulin injury. Journal of Neurosurgery: Pediatrics. 2015; 16(4): 420–425, doi:
resistance in type 2 diabetic patients. Diabetes Research and Clinical 10.3171/2015.3.peds14521.
Practice. 2008; 79(2): 237–242, doi: 10.1016/j.diabres.2007.08.029. 46. Udovcic M, Pena R, Patham B, et al. Hypothyroidism and the Heart.
36. Kozera G, Neubauer-Geryk J, Wolnik B, et al. Cerebral and skin micro- Methodist DeBakey Cardiovascular Journal. 2017; 13(2): 55–59, doi:
circulatory dysfunction in type 1 diabetes. Advances in Dermatology 10.14797/mdcj-13-2-55.
and Allergology. 2019; 36(1): 44–50, doi: 10.5114/ada.2018.81185. 47. Kavitha Y, Joish U, Reddy R, et al. Doppler indices of superior thyroid
37. Kozera G, Dubaniewicz M, Zdrojewski T, et al. Cerebral Vasomotor artery in clinically euthyroid adults. Indian Journal of Radiology and
Reactivity and Extent of White Matter Lesions in Middle-Aged Men With Imaging. 2018; 28(1): 10, doi: 10.4103/ijri.ijri_194_17.
Arterial Hypertension: A Pilot Study. American Journal of Hypertension. 48. Owecki M, Sawicka-Gutaj N, Owecki M, et al. Pulsatility Index in
2010; 23(11): 1198–1203, doi: 10.1038/ajh.2010.152. Carotid Arteries is Increased in Levothyroxine-Treated Hashimoto
38. Janssen A. Pulsatility index is better than ankle-brachial doppler index Disease. Hormone and Metabolic Research. 2015; 47(08): 577–580,
for non-invasive detection of critical limb ischaemia in diabetes. Vasa. doi: 10.1055/s-0034-1398491.
2005; 344: 235–241. 49. Kalantari S. The Diagnostic Value of Color Doppler Ultrasonography
39. Cheng SH, Wang J, Xu GH, et al. Effect of Noaxintong Capsule on in Predicting Thyroid Nodules Malignancy. The International Tinnitus
Vascular Remodelin in Type 2 Diabetic Patients with Subclinical Va- Journal. 2018; 22(1), doi: 10.5935/0946-5448.20180006.
scular Disease. Zhongguo Zhong Xi Yi Jie He Za Zhi. 2016; 36(12): 50. Asil T, Uzunca I, Utku U, et al. Monitoring of Increased Intracranial
1439–1444. Pressure Resulting From Cerebral Edema With Transcranial Dop-
40. Park J, Cho M, Lee K, et al. The effects of pioglitazone on cerebrova- pler Sonography in Patients With Middle Cerebral Artery Infarction.
scular resistance in patients with type 2 diabetes mellitus. Metabolism. Journal of Ultrasound in Medicine. 2003; 22(10): 1049–1053, doi:
2007; 56(8): 1081–1086, doi: 10.1016/j.metabol.2007.03.017. 10.7863/jum.2003.22.10.1049.
41. Schöning M, Hartig B. The development of hemodynamics in 51. Bor-Seng-Shu E, Figueiredo E, Fonoff E, et al. Decompressive craniec-
the extracranial carotid and vertebral arteries. Ultrasound in tomy and head injury: brain morphometry, ICP, cerebral hemodynamics,
Medicine & Biology. 1998; 24(5): 655–662, doi: 10.1016/s0301- cerebral microvascular reactivity, and neurochemistry. Neurosurgical
5629(98)00029-5. Review. 2013; 36(3): 361–370, doi: 10.1007/s10143-013-0453-2.
42. Schöning M, Walter J, Scheel P. Estimation of cerebral blood flow 52. Obwieszczenie Ministra Zdrowia z dnia 4 grudnia 2019 r w sprawie
through color duplex sonography of the carotid and vertebral arteries in sposobu i kryteriów stwierdzenia trwałego nieodwracalnego ustania
healthy adults. Stroke. 1994; 25(1): 17–22, doi: 10.1161/01.str.25.1.17. czynności mózgu.
210 www.journals.viamedica.pl/medical_research_journal