Literature DB >> 22811907

Doppler parameters of hepatic and renal hemodynamics in patients with liver cirrhosis.

D Popov1, R Krasteva, R Ivanova, L Mateva, Z Krastev.   

Abstract

Introduction. There are limited studies on simultaneous evaluation of liver and renal blood flow using Doppler methods. We evaluated and compared the changes of liver and renal Doppler US parameters in patients with liver cirrhosis according to the degree of liver disease. Material and Methods. We assessed a large spectrum of liver and renal Doppler US parameters in 67 patients with liver cirrhosis. Results. Significant differences between Child's classes or score, as well as MELD score, were observed in all investigated intrarenal blood flow Doppler US parameters, except renal artery peak systolic velocity, but only in some of the hepatic ones. The deviations of renal Doppler US parameters were also related with the complications of liver cirrhosis, as well as serum urea and creatinine levels. There was relationship between Doppler US parameters of hepatic artery and the corresponding renal artery Doppler US parameters. The changes of Doppler US parameters were age independent. Conclusion. Our results show, renal Doppler US parameters correlate with the severity and complications of liver cirrhosis. Because of dynamic deviations of renal Doppler US parameters with advance of liver cirrhosis, we recommend Doppler US of renal artery as a part of follow up of these patients.

Entities:  

Year:  2012        PMID: 22811907      PMCID: PMC3397178          DOI: 10.1155/2012/961654

Source DB:  PubMed          Journal:  Int J Nephrol


1. Introduction

Portal hypertension is the most important feature of liver cirrhosis and its complications. In addition, kidney dysfunction, especially renal vasoconstriction, plays important role in the hepatorenal syndrome and patient's prognosis [1]. The detailed investigation of the renal blood flow in real time is a challenge for the investigators. Many authors evaluate the hemodynamics of portal vein and hepatic arterial blood flow, as well as renal arterial blood flow [2-20]. There are limited studies on simultaneous evaluation of liver and renal blood flow using Doppler methods in real time [21]. Because of that, the aim of our study was to evaluate and compare the changes of liver and renal Doppler US parameters in patients with liver cirrhosis according to the degree of liver disease. We also assess the relationship between these parameters and some surrogate markers of renal function.

2. Material and Methods

A total of 67 in-patients with liver cirrhosis were investigated from 2008 to 2010 year. The main characteristic of the patients with liver cirrhosis was given on Table 1. All patients were treated with Silymarine or vitamins and in addition 39 patients with esophageal varices took beta-blockers (Propranolol), and 42 patients took diuretics (18-Spironolactone, 2—Furosemide, and 22—Spironolactone plus Furosemide). Hypertension (n = 27) was the most frequent concomitant disease, but well controlled with the therapy of beta-blockers and/or diuretics. The other comorbidity included diabetes mellitus (n = 13), cholelithiasis (n = 12), chronic gastritis (n = 9), ischaemic heart disease (n = 8), chronic bronchitis (n = 6), chronic pancreatitis (n = 5), chronic gastroduodenal ulcer (n = 6), gastro-reflux esophageal disease (n = 5), cerebrovascular disease (n = 4), diverticulosis (n = 2), and others (n = 14).
Table 1

Characteristics of patients with liver cirrhosis.

ParametersAll patients (n = 67)Child A (n = 33)Child B (n = 22)Child C (n = 12)
Age (x ± SD)54.22 ± 12.3656.85 ± 12.2651.45 ± 12.7552.08 ± 11.34
Sex—m/f39/2817/1614/88/4
Etiology (n)
 Alcohol2551010
 Viral3726101
 Study approved211
 Autoimmune3111
 Others
LC (n)
 Compensated322930
 Decompensated3541912
Esophageal varices (n)
 Yes/no49/1823/1014/812/0
Ascites (n)
 Yes/no26/412/3113/911/1
Encephalopathy (n)
 Yes/no8/590/332/206/6
MELD score (x ± SD)15.01 ± 7.1710.90 ± 3.2915.32 ± 3.6725.75 ± 8.64
Therapy with (n):
 B-blockers—Yes/no39/2815/1816/68/4
 Diuretics—Yes/no42/2516/1715/711/1
Comorbidity (n)
 Yes/no50/1728/514/88/4
The study was approved by the Institutional Review Committee Board and informed consent for the trial was obtained from each person. The patients with gastrointestinal bleeding and or endoscopic band ligation or sclerotherapy in the last 8 weeks, surgery, thrombosis portal veins, liver tumors, extrahepatic cholestasis, acute alcoholic hepatitis, hepatorenal syndrome, therapy with vasoactive drugs, excluding beta-blockers and diuretics, significant concomitant disease and cotherapy, which might interfere Doppler ultrasound parameters, and renal function were excluded. Abdominal ultrasound (US), as well as liver and renal Doppler US, was performed and interpreted by one investigator according to standard protocol. US measurements were done by Aloka SSD 4000, convex probe 2.5–5,0 MHz, cut-off filter 100 Hz, with angle of insonation 50°, using a 2–3,5-5 mm Doppler gate, as large as at least one-third of the vessel diameter. The investigated subjects fasted over night and rest in bed in the supine position for at least 10 minutes before the US measurements. Portal vein (PV), hepatic artery (HA), and intrarenal arteries (RAs), interlobar or segmental branch, were evaluated by Color Doppler US. A rectilinear segment of the common tract of the portal vein (PV), as near as possible to the bifurcation, was estimated. The proper hepatic artery (HA) was investigated near the point where it crosses the main PV. A train of at least three similar, sequential Doppler waveforms was obtained during suspended respiration, sometimes in sustained shallow inspiration. Three Doppler waveform tracings were obtained from each kidney by sampling the RA: right (RRA-RA) and left (LRA-RA) in the superior, middle, and inferior portions of the kidney. The mean values of the parameters, for each kidney, were obtained from the measurement of the waveforms of both, right and left renal area. We evaluated the following hepatic and intrarenal blood flow Doppler parameters (cm/sec): PV peak systolic velocity (PV-PSV), portal venous time-averaged maximum velocity (PVV = PV-PSV × 0,57), HA maximum peak systolic velocity (HA-PSV), HA minimal end diastolic velocity (HA-EDV), HA mean velocity (HA-MnV = HA-PSV × 0,62), HA resistance index (HA-RI = HA-PSV − HA-EDV/HA-PSV), HA pulsatility index (HA-PI = HA-PSV − HA-EDV/HA-MnV), liver vascular index (LVI = PVV/HA-PI), modified liver vascular index (mLVI = PVV/HA-RI), arterio/portal ratio (A/P = HA-PSV/PV-PSV), RA peak systolic velocity (RA-PSV), RA minimal end diastolic velocity (RA-EDV), RA mean velocity (RA-MnV), RA resistance index (RA-RI = RA-PSV − RA-EDV/RA-PSV), and RA pulsatility index (RA-PI = RA-PSV − RA-EDV/RA-MnV). The diagnosis of liver cirrhosis was based on standard criteria. Besides the standard hematological and biochemical tests, we also tested urine sodium excretion (mmol/24 h), glomerular filtration rate (GFR, mL/min), and correct GFR (GFR × 1,73/body surface, mL/min). For evaluation of the degree of liver damage we used Child-Pugh classification of liver cirrhosis [22] and MELD [23]. Statistical analysis was performed using ANOVA, Mann-Whitney, and correlation analyses (SPSS v.14). P value less than 0.05 was considered as statistically significant.

3. Results

3.1. Liver Doppler US Parameters

3.1.1. Relationship between Liver Doppler US Parameters and Severity of Liver Cirrhosis

From all evaluated liver Doppler US parameters significant differences among Child's class A, B, and C were observed only for the peak systolic velocity of PV, liver, and modified liver vascular indices (Table 2). We also found significant relationship between Child's score and PV time-averaged maximum velocity, PV peak systolic velocity, and liver vascular index values. On the other hand HA mean velocity, HA maximum peak systolic velocity, and arterio/portal ratio were higher in patients with MELD score more than 20 compared to the patients with MELD score less than 20 (Table 3). There was no correlation between values of liver Doppler US parameters and MELD score.
Table 2

Liver Doppler US parameters in patients with liver cirrhosis according to Child-Pugh classification.

ParameterAll patients (n = 67)Child A (n = 33)Child B (n = 22)Child C (n = 12)Child's score (5–15 points)
Mean ± SDMean ± SDMean ± SDMean ± SDCorrelation (r)
PVV16.35 ± 3.4915.68 ± 3.3516.49 ± 3.0317.94 ± 4.32 0.268, P = 0.028
PV-PSV28.68 ± 6.1227.51 ± 5.8728.93 ± 5.3231.46 ± 7.59P = 0.0450.268P = 0.028
HA-PSV69.60 ± 20.5570.23 ± 21.0767.58 ± 16.3071.56 ± 26.86
HA-MnV43.23 ± 12.7343.49 ± 13.0742.22 ± 10.0944.39 ± 16.67
HA-EDV23.41 ± 7.1322.78 ± 7.3023.86 ± 6.6524.33 ± 7.96
HA-RI0.66 ± 0.070.67 ± 0.040.64 ± 0.070.65 ± 0.10
HA-PI1.06 ± 0.121.09 ± 0.081.03 ± 0.131.04 ± 0.17
A/P2.50 ± 0.782.60 ± 0.732.39 ± 0.672.43 ± 1.08
LVI15.73 ± 4.3714.55 ± 3.5516.18 ± 3.3618.13 ± 6.75P = 0.041 0.282 P = 0.021
mLVI25.21 ± 6.8825.21 ± 6.8826.04 ± 5.5028.47 ± 10.60P = 0.041
Table 3

Liver Doppler US parameters with significant differences according to MELD score.

Parameter MELD N MeanSD95% confidence interval for meanMinimumMaximum P
Lower boundUpper bound
HA-MnV<205541.3210.4538.4944.1422.3071.360.007
>201252.0118.2940.3963.6224.3784.60
HA-PSV<205566.4916.8561.9371.0436.00115.100.007
>201283.8529.4865.12102.5839.30136.40
A/P<20552.410.632.242.581.154.070.029
>20122.951.202.183.711.014.81

3.1.2. Relationship between Liver Doppler US Parameters and Complications of Liver Cirrhosis

There were no significant differences between liver Doppler US parameters and the presence of esophageal varices and collaterals and among patients with compensated and decompensated liver cirrhosis, as well as patients with or without ascites, or portal encephalopathy.

3.2. Renal Doppler US Parameters

3.2.1. Relationship between Renal Doppler US Parameters and Severity of Liver Cirrhosis

All intrarenal blood flow Doppler parameters except right and left RA peak systolic velocity showed significant differences between Child's class A, B, and C (Table 4). In addition we also found a significant relationship between Child's score and right and left RA minimal end diastolic velocity, right and left RA resistance, and RA pulsatility indices.
Table 4

Renal Doppler US parameters in patients with liver cirrhosis according to Child-Pugh classification.

ParameterAll patients (n = 67)Child A (n = 33)Child B (n = 22)Child C (n = 12)Child's score (5–15 points)
Mean ± SDMean ± SDMean ± SDMean ± SDCorrelation (r)
RRA-PSV56.06 ± 11.2457.47 ± 11.0755.33 ± 11.0753.53 ± 11.29
LRA-PSV55.79 ± 12.3656.56 ± 13.2756.69 ± 11.4452.01 ± 11.62
RRA-MnV31.62 ± 7.3632.73 ± 6.6532.63 ± 7.9626.70 ± 6.59P = 0.046
LRA-MnV31.10 ± 7.6131.85 ± 7.7932.67 ± 7.0426.17 ± 6.59P = 0.040
RRA-EDV19.07 ± 5.4019.88 ± 4.7820.07 ± 5.6615.00 ± 5.01P = 0.013−0.400P = 0.001
LRA-EDV18.17 ± 5.3318.60 ± 5.2719.45 ± 5.0414.62 ± 4.80P = 0.031−0.298P = 0.014
RRA-RI0.66 ± 0.060.65 ± 0.050.64 ± 0.050.72 ± 0.09P = 0.0010.456P = 0.0001
LRA-RI0.67 ± 0.070.67 ± 0.050.65 ± 0.060.71 ± 0.09P = 0.0330.349P = 0.004
RRA-PI1.21 ± 0.301.17 ± 0.171.10 ± 0.171.51 ± 0.51P = 0.00010.532P = 0.001
LRA-PI1.23 ± 0.271.20 ± 0.211.15 ± 0.191.47 ± 0.41P = 0.0020.489P = 0.001
According to MELD score a significant decrease of right and left RA mean velocity and minimal end diastolic velocity and an increase of right and left RA resistance and RA pulsatility indices were observed in patients with MELD <20 versus those with MELD >20 (Table 5). We also found correlations between those renal Doppler parameters and MELD score. Only values of right and left RA peak systolic velocity showed no significant change.
Table 5

Renal Doppler US parameters in patients with liver cirrhosis according to MELD score.

Parameter MELD N MeanSD95% confidence interval for mean Minimum Maximum P MELD score (8–46)
Lower boundUpper bound Correlation (r)
<205532.307.1330.3834.2319.9049.10
RRA-MnV>201228.477.8823.4633.4713.8039.90NS −0.396 P = 0.001
Total6731.627.3629.8233.4113.8049.10

<205531.377.1529.4333.3017.1049.90
LRA-MnV>201229.899.7323.7136.0814.9053.50NS −0.294 P = 0.016
Total6731.107.6129.2532.9614.9053.50

<205519.805.1418.4121.1911.3032.30
RRA-EDV>201215.715.4612.2419.186.8024.200.016 −0.459 P = 0.001
Total6719.075.4017.7520.396.8032.30

<205518.514.7517.2219.7910.2030.70
LRA-EDV>201216.617.4811.8621.366.9035.20NS −0.358 P = 0.003
Total6718.175.3316.8719.476.9035.20

<20550.650.050.630.660.560.79
RRA-RI>20120.730.070.680.7700.650.860.0001 0.552 P = 0.0001
Total670.660.060.650.680.560.86

<20550.660.060.640.670.530.77
LRA-RI>20120.740.070.690.780.610.820.0001 0.477 P = 0.001
Total670.670.070.660.690.530.82

<20551.130.171.081.170.871.57
RRA-PI>30121.560.471.271.861.132.620.0001 0.604 P = 0.0001
Total671.210.301.131.280.872.62

<20551.160.191.111.220.781.78
LRA-PI>30121.560.351.331.781.012.220.0001 0.564 P = 0.0001
Total671.230.271.171.300.782.22

3.2.2. Relationship between Renal Doppler US Parameters and Complications of Liver Cirrhosis

In patients with esophageal varices we observed a decrease of right (P = 0.002) and left (P = 0.038) RA mean velocity, right RA peak systolic velocity (P = 0.045), as well as right (P = 0.003) and left RA minimal end diastolic velocity (P = 0.025) compared to the values of subjects without esophageal varices (Figure 1). There was no significant difference between renal Doppler US parameters in patients with or without collaterals.
Figure 1

The values of RRA/LRA-MnV, RRA/LRA-PSV and RRA/LRA-EDV in patients with presence or absence of esophageal varices.

In comparison of patients with compensated and decompensated liver cirrhosis we found a significant decrease of right RA minimal end diastolic velocity (P = 0.021), as well as an increase of right (P = 0.020) and left (P = 0.028) RA resistance index and right (P = 0.024) and left (P = 0.002) RA pulsatility index (Figures 2, 3, and 4). The right and left RA mean velocity (P = 0.015) and left RA minimal end diastolic velocity (P = 0.027) were also decreased in patients with ascites than those without ascites (Figure 5). In patients with portal encephalopathy we observed significant increase of right RA resistance index (P = 0.014), as well as right (P = 0.003) and left (P = 0.005) RA pulsatility index than subjects without portal encephalopathy (Figures 6 and 7).
Figure 2

The values of RRA/LRA-EDV in patients with compensated and decompensated liver cirrhosis.

Figure 3

The values of RRA/LRA-RI in patients with compensated and decompensated liver cirrhosis.

Figure 4

The values of RRA/LRA-PI in patients with compensated and decompensated liver cirrhosis.

Figure 5

The values of RRA/LRA-MnV and RRA/LRA-EDV in patients with presence or absence of ascites.

Figure 6

The values of RRA/LRA-RI in patients with presence or absence of hepatic encephalopathy.

Figure 7

The values of RRA/LRA-PI in patients with presence or absence of hepatic encephalopathy.

3.3. Relationship between Liver and Renal Doppler US Parameters

We observed correlations between Doppler US parameters of hepatic artery and arterio/portal ratio by one hand and some renal Doppler US parameters on the other hand (Table 6).
Table 6

Significant correlations between liver and renal Doppler US parameters.

Surrogate markers of renal functionParametersPearson correlation P
RRA-MnV0.2520.040
HA-PSVRRA-PSV0.3470.004
LRA-PSV0.3630.003

RRA-MnV0.2500.041
HA-MnVRRA-PSV0.3430.005
LRA-PSV0.3550.003

RRA-MnV0.2780.023
LRA-MnV0.2660.030
HA-EDVRRA-EDV0.3010.013
RRA-EDV0.2870.019
LRA-PSV0.2670.029

RRA-RI0.4460.0001
LRA-RI0.5280.0001
HA-RIRRA-PI0.3870.001
LRA-RI0.4510.001
LRA-EDV−0.2500.041

RRA-PSV0.2440.047
RRA-RI0.4160.0001
HA-PILRA-RI0.4770.0001
RRA-PI0.3440.004
LRA-RI0.3940.001

A/PRRA-PSV0.2840.020

3.4. Surrogate Markers of Renal Function

Serum urea levels and serum sodium levels correlated with Child's and MELD scores (Table 7). Serum urea and serum creatinine levels showed significant correlation with some renal Doppler US parameters, but not with liver Doppler US parameters. GFR, correct GFR, and urine sodium excretion showed no significant relationships.
Table 7

Significant correlations between surrogate markers of renal function and Childs and MELD scores, and renal Doppler US parameters.

Surrogate markers of renal functionParametersPearson correlation P
Serum ureaChild's score0.3530.012
MELD score0.4350.002
LRA-MnV−0.2940.036
LRA-EDV−0.3130.025
RRA-RI0.2970.035
RRA-PI0.2960.035
LRA-PI0.2800.046

Serum creatinineRRA-MnV−0.3460.005
LRA-MnV−0.3260.008
RRA-EDV−0.3500.004
LRA-EDV−0.3170.010

Serum sodiumChild's score−0.4230.001
MELD score−0.4850.0001

3.5. Impact of Patient's Age on Liver and Renal Doppler US Parameters

We observed relationship between patient's age and some liver Doppler US parameters as HA minimal end diastolic velocity (r = −262, P = 0.032), liver vascular index (r = −240, P = 0.05), and modified liver vascular index (r = −247, P = 0.044). On the other hand, no significant correlation between patient's age and renal Doppler US parameters was found. Among the surrogate markers of kidney function, only the values of GFR (r = −571, P = 0.0001) and correct GFR (r = −536, P = 0.0001) showed significant inverse correlation.

4. Discussion

Many liver Doppler US parameters and indices have been used to distinguish the patients with portal hypertension from those with normal hemodynamic of portal vein and hepatic arterial blood flow [2–7, 10]. But there are confusing data when comparing their changes according to Child's classes or MELD, as well as the presences of complications of liver cirrhosis [2, 5–7, 9, 24–26]. In this study we evaluated and compared the changes of large number of liver and renal Doppler US parameters, measured simultaneously in patients with liver cirrhosis according to the degree of liver disease. Our results show that PV time-averaged maximum velocity and peak systolic velocity, as well as liver and modified liver vascular indices, are associated with Child-Pugh classes. Some authors also reported the relationship between some liver Doppler US parameters and Child's classes, as well as an appearance of pseudonormalisation of portal vein hemodynamic when liver cirrhosis advances [5–7, 9–12, 24, 25]. However, Child-Pugh score is not the perfect system for the assessment of degree of liver cirrhosis and it has some limitations, including the subjective interpretation of ascites and encephalopathy, and some laboratory deviations, especially prothrombin time. Because of that we also use MELD as one universal system for the assessment of severity of liver cirrhosis [23]. Hepatic artery mean velocity, HA maximum peak systolic velocity, and arterio/portal ratio were higher in patients with MELD score more than 20 compared to the patients with MELD score below 20. On the other hand, no one of the liver Doppler US parameters correlate directly with MELD score. In addition, there were no significant differences between liver Doppler US parameters and various complications of liver cirrhosis. As a whole, our results confirm the buffer role of hepatic artery with advance of liver cirrhosis and pseudonormalisation of some liver Doppler US parameters. One possible reason for the contradicting data in the literature is the heterogenity of patients with liver cirrhosis, included in various studies. The differences also depend on the type of hemodynamic disturbances, for example, the presence of hyperkinetic syndrome or collaterals [5, 9]. Many other factors also interfere with values of liver Doppler US parameters in patients with liver cirrhosis [2, 4, 5, 21]. Acute alcoholic hepatitis and other significant concomitant diseases are exclusion criteria in our study. Despite of that, more than one-third of our patients have an alcoholic etiology of liver cirrhosis, ten patients have collaterals, and more than 50% of the patients take beta-blockers and diuretics. Our data show relationship between patient's age and HA minimal end diastolic velocity, liver vascular index, and modified liver vascular index and confirm the role of age for the deviations of these Doppler US parameters. The evaluation of the renal hemodynamics in patients with liver cirrhosis is based mainly on the index of resistance of the intrarenal arteries [11-20]. Renal vasoconstriction has been documented in several series of cirrhotic patients on the base of increased resistive index [1]. In patients with refractory ascites, as well as in subjects with serum creatinine within the normal range, increased RI seems to be correlated with a higher risk of subsequent deterioration in renal function [1, 12, 15, 17–20]. In our study in contrast to liver Doppler US parameters, all intrarenal blood flow Doppler parameters except RA peak systolic velocity show a significant association with the severity of liver cirrhosis, evaluated by both Child's and MELD scores. Most of these parameters also correlate with the presence of esophageal varices and ascites, as well as with the decompensation of liver cirrhosis. In addition some renal Doppler US parameters, but no one of liver Doppler US parameters, correlate with serum urea and serum creatinine levels. Similar results were reported when comparing patients with liver cirrhosis with and without ascites and with first signs of renal failure [13, 20]. The data about correlation between RI and the glomerular filtration are controversial [1, 13]. The increase of creatinine level corresponds to the higher values of the impedance indices. Renal artery Doppler US parameters may be useful for identifying patients at high risk for developing impaired renal function at an early stage. On the other hand, there is no evidence that Doppler US helps differentiate cirrhotic patients with impaired renal function only related to vasoconstriction from patients who have both vasoconstriction and intrinsic kidney damage. The values of renal Doppler US parameters also depend on many factors [1, 14]. The application of diuretics leads to an elevation in the impedance indices of the intrarenal arteries. Paracentesis and albumin infusion are followed by a significant decrease in renal RI. Because of that, renal artery Doppler US may help to clarify the role of therapeutic intervention on renal hemodynamics. In our study the therapy of beta-blockers and diuretics, as well as concomitant cardio-vascular disease or diabetes, may interfere with the renal blood flow. On the other hand, our data show no correlation between patient's age and renal Doppler US parameters. These results are in conflict with the data in subjects without liver cirrhosis. The simultaneous measurement of liver and renal Doppler US parameters allows to find relationships between Doppler US parameters of hepatic artery and the corresponding renal artery Doppler US parameters. These data emphasize common pathophysiological mechanisms for impairment of hepatic and renal artery blood flow. On the other hand, renal Doppler US parameters show more dynamic deviations than liver Doppler US parameters in advance of liver cirrhosis and may need to be evaluated in follow-up of these patients. In conclusion, our results show parallel changes in renal and hepatic artery Doppler US parameters in patients with liver cirrhosis, independently of patient's age. There is no direct correlation between the degree or complications of liver cirrhosis and most of liver Doppler US parameters. In contrast, renal Doppler US parameters correlate with the severity and complications of liver cirrhosis. Because of dynamic deviations of renal Doppler US parameters in advance of liver cirrhosis, we recommend Doppler US of renal artery as a part of the followup of these patients.
  24 in total

1.  Value of splanchnic Doppler ultrasound in the diagnosis of portal hypertension.

Authors:  F Piscaglia; G Donati; C Serra; R Muratori; L Solmi; S Gaiani; L Gramantieri; L Bolondi
Journal:  Ultrasound Med Biol       Date:  2001-07       Impact factor: 2.998

2.  Doppler and gray-scale ultrasound evaluation of morphological and hemodynamic changes in liver vascualture in alcoholic patients.

Authors:  Sumru Cosar; Suna O Oktar; Behcet Cosar; Cem Yücel; Hakan Ozdemir
Journal:  Eur J Radiol       Date:  2005-06       Impact factor: 3.528

3.  Renovascular impedance correlates with portal pressure in patients with liver cirrhosis.

Authors:  Annalisa Berzigotti; Andrea Casadei; Donatella Magalotti; Nicola Castaldini; Francesco Losinno; Cristina Rossi; Marco Zoli
Journal:  Radiology       Date:  2006-06-26       Impact factor: 11.105

4.  Duplex-Doppler ultrasonography in the assessment of portal hypertension. Utility of the measurement of maximum portal flow velocity.

Authors:  P D'Alimonte; G Cioni; A Cristani; A Ferrari; E Ventura; R Romagnoli
Journal:  Eur J Radiol       Date:  1993-09       Impact factor: 3.528

Review 5.  The evaluation of renal function and disease in patients with cirrhosis.

Authors:  Claire Francoz; Denis Glotz; Richard Moreau; François Durand
Journal:  J Hepatol       Date:  2010-01-07       Impact factor: 25.083

6.  Hepatic flow parameters measured with MR imaging and Doppler US: correlations with degree of cirrhosis and portal hypertension.

Authors:  Laurence Annet; Roland Materne; Etienne Danse; Jacques Jamart; Yves Horsmans; Bernard E Van Beers
Journal:  Radiology       Date:  2003-09-11       Impact factor: 11.105

7.  Abnormal renovascular impedance in patients with hepatic cirrhosis: detection with duplex US.

Authors:  A Colli; M Cocciolo; C Riva; E Martinez
Journal:  Radiology       Date:  1993-05       Impact factor: 11.105

8.  Renal duplex Doppler ultrasonography: a noninvasive predictor of kidney dysfunction and hepatorenal failure in liver disease.

Authors:  J F Platt; J H Ellis; J M Rubin; R M Merion; M R Lucey
Journal:  Hepatology       Date:  1994-08       Impact factor: 17.425

9.  Diagnosis of functional kidney failure of cirrhosis with Doppler sonography: prognostic value of resistive index.

Authors:  A Maroto; A Ginès; J Saló; J Clària; P Ginès; L Anibarro; W Jiménez; V Arroyo; J Rodés
Journal:  Hepatology       Date:  1994-10       Impact factor: 17.425

10.  Value of measurement of mean portal flow velocity by Doppler flowmetry in the diagnosis of portal hypertension.

Authors:  G Zironi; S Gaiani; D Fenyves; A Rigamonti; L Bolondi; L Barbara
Journal:  J Hepatol       Date:  1992-11       Impact factor: 25.083

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Authors:  Kambiz Akhavan Rezayat; Abbas Ali Zeraati; Masoud Pezeshki Rad; Jalal Chogan; Najmeh Davoudian; Amir Akhavan Rezayat; Seyed Mousalreza Hoseini
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