Ultrasound Screening for Vascular Disease

Introduction

Medical screening is the process of using a diagnostic algorithm to detect a disease or the susceptibility to develop a disease. A screening process can consist of a medical history, a blood sample that measures a biochemical marker such as cholesterol, or medical imaging to detect a morphological or functional trait. The screening process is normally applied to a patient population with predefined characteristics. The ultimate applicability of the screening process weighs the potential benefits of detecting and treating the individuals identified against the total costs to society. This form of public health screening is different from performing individual screening with the costs borne not by society but by the individual being screened.

This chapter focuses on the noninvasive approaches to arterial disease screening and focuses on B-mode (gray-scale) and Doppler ultrasound imaging in asymptomatic individuals. The goal is to identify, from a large group of individuals, a smaller subset with a high likelihood of disease so that some form of intervention can be selected and applied with the hope of decreasing disease morbidity. This approach is typically used in primary prevention. This means that the patient being screened is completely asymptomatic.

Some clinical scenarios are not covered in this chapter. For example, a patient with a prior lower extremity bypass graft who has undergone a Doppler ultrasound examination is not considered as being screened because the patient obviously has peripheral vascular disease. The patient is undergoing surveillance, a form of secondary prevention (i.e., the Doppler ultrasound is used to identify a bypass graft at risk of occlusion). In another scenario, a patient having had a recent stroke then undergoes a carotid ultrasound examination. This examination is not considered a screening test but is part of the clinical workup. In this instance, the goal is to detect a significant carotid artery stenosis that might have caused the neurologic event and then to treat it. This is also a form of secondary prevention because the patient already has the clinical outcome and the goal is now to prevent recurrent strokes.

This chapter will review some generic aspects of the screening process and then address three specific screening applications: (1) use of color and duplex Doppler ultrasound to detect significant carotid artery stenosis in asymptomatic individuals; (2) use of ultrasound to detect abdominal aortic aneurysms; and (3) use of carotid ultrasound to detect high-risk individuals for the presence of subclinical atherosclerosis.

Definition and Types of Screening

What is screening? The different elements of a screening process have been clearly presented in a World Health Organization (WHO) bulletin published in 1968. These basic principles are listed in Table 33.1 . Certain criteria have to be met for the screening process to be successful. These criteria will be discussed in the context of the three screening protocols reviewed later in this chapter.

TABLE 33.1

Principles of Screening. ^a

1.
The condition sought should be an important health problem.

2.
There should be an accepted treatment for patients with recognized disease.

3.
Facilities for diagnosis and treatment should be available.

4.
There should be a recognizable latent or early symptomatic stage.

5.
There should be a suitable test or examination.

6.
The test should be acceptable to the population.

7.
The natural history of the condition, including development from latent to declared disease, should be adequately understood.

8.
There should be an agreed policy on whom to treat as patients.

9.
The cost of case finding (including diagnosis and treatment of patients diagnosed) should be economically balanced in relation to possible expenditure on medical care as a whole.

10.
Case finding should be a continuing process and not a “once and for all” project.

a As presented by Wilson and Jungner in the World Health Organization Public Health Paper no. 34, Principles and Practice of Screening for Disease (1968).

The WHO bulletin describes three specific types of screening: selective screening, mass public health screening, and surveillance ( Table 33.2 ).

TABLE 33.2

Differences Between Types of Screening.

	Selective Screening	Mass Screening	Surveillance Screening
Advantages	Appropriate for individuals	Applied to whole population	Applied to subset with precursor lesion and at highest risk of developing a clinical outcome
Advantages	Decrease in costs compared with mass screening	Unlikely to miss individuals at risk	Permits timing of intervention
Disadvantages	Expensive: high cost per individual	Expensive: low cost but for many individuals	Expensive: repeat examinations over time
	Even low-risk individuals might have the lesion	False positives are very likely	Requires motivation to have repeat examinations
	Requires individual motivation	Large infrastructure needed to perform reliable test	Psychological effect of having a biological time bomb

Selective screening

The selective screening approach is the application of a diagnostic test to a predetermined asymptomatic population whose members have been selected because they have one or more risk factors. The risk factors are different from the screening tool. For example, a clinical history of cigarette smoking is a risk factor for aneurysm formation. The yield of an abdominal ultrasound will therefore be greater in smokers than in nonsmokers. The problem with this approach is that the individual who has never smoked can still have an aneurysm, although the odds are much lower than for the smoker. However, being a nonsmoker would exclude the individual from the screening ultrasound.

Mass public screening

The second type of screening is a mass public screening. With this approach, the same test is used in the whole population. As commonly applied, mass screening is still selective because the individuals being screened are often selected on the basis of a specific demographic such as age and applied to those living in a given geographic location. Testing young children for low thyroid hormone levels is an example of such a screening process. The screen is then applied to children and not adults. Additional focus may be given to a geographic region where iodine deficiency may exist. The basic limitation with this approach is increased cost.

Surveillance screening

The third type of screening is surveillance screening. The WHO criteria indicate that the disease being screened for should have a defined natural history and an available treatment and/or intervention. For example, a patient is found to have an ectatic abdominal aorta with a diameter of 2.5 cm. Although the aortic diameter is less than the 3 cm threshold used to define an aneurysm, there is a strong likelihood that this aortic segment will continue to dilate and become an aneurysm over the next 5 to 10 years. The patient's aortic diameter will need to be monitored because the risk of aneurysm formation is increased. Antihypertensive therapy and smoking cessation may have some impact at this early stage of the disease. The appropriate time interval for the surveillance examinations needs to be determined and justified.

Practical Tips

There are three types of screening:
- mass screening
- selective screening
- surveillance screening
Ultrasound imaging is more likely to be used for selective and surveillance screening.

Screening for Asymptomatic Carotid Stenosis

The goal of a carotid ultrasound screening examination is the detection of individuals who are asymptomatic, are at risk of stroke, and would benefit from an operative intervention such as carotid endarterectomy or endovascular stent placement. The Doppler screening criteria need to correlate with those of carotid arteriography because the benefits of carotid interventions are based on measurements of disease severity made with arteriography. This assumes there is a cut-point above which, by arteriography, a carotid stenosis is considered significant and an intervention decreases the risk of future stroke. The question then becomes how accurate is a Doppler ultrasound in detecting a stenosis and grading it when compared with arteriography?

Prevalence of significant carotid stenosis

Published Doppler velocity cut points that are used to grade carotid artery stenosis severity are typically obtained from departments or vascular laboratories with a patient population having a high prevalence of carotid artery disease. This skewed perspective is made worse by the selection process that leads to the patient having a carotid arteriogram. These two factors contribute to a bias toward a high prevalence of disease. In essence, arteriography is being performed after the carotid ultrasound because there is a high suspicion of significant disease. Data obtained from publications correlating internal carotid artery peak systolic velocities with carotid angiography show this bias. The distribution of measured carotid Doppler peak systolic velocities is bimodal (i.e., there are two peaks) ( Fig. 33.1 ). The first peak is a mixture of false positives and relatively normal carotid bifurcations contralateral to the side of the lesion. The second peak includes the target lesions. This information does not give much insight into how carotid ultrasound might perform as a screening test in the general population.

FIG. 33.1, (A) Actual distribution of peak systolic velocity obtained from a series of published papers correlating Doppler velocities with carotid angiography. 5 6 7 8 9 10 11 12 The second peak ( arrow ) is caused by the preselection of individuals with abnormal Doppler velocities and a prevalence of internal carotid artery stenosis ≥50%. (B) These data have been modified to decrease the prevalence of angiographic stenosis ≥50%. The amplitude of the second curve has significantly decreased and disease prevalence has dropped to 27%.

The distribution of carotid disease can be estimated using Doppler velocities as a surrogate for carotid artery stenosis. Ideally, the true prevalence would be estimated by scanning the whole population, however this is not feasible based on simple economics. The alternative is to perform ultrasound in epidemiologic cohorts. These cohorts, such as the Framingham Heart Study (FHS), the Cardiovascular Health Study (CHS), and the Multi-Ethnic Study of Atherosclerosis (MESA) have a representative sampling of the general population. Carotid Doppler examinations in members of these cohorts show a very different pattern of disease from that seen in Doppler validation studies. In essence, the distribution shows a large primary peak and a taper into the high-velocity (stenosis) values ( Fig. 33.2 ). This sampling from the general population gives a better insight into using carotid artery Doppler ultrasound as a method to detect significant carotid artery disease in asymptomatic individuals within the general population.

FIG. 33.2, The distribution of carotid artery disease in two epidemiologic cohorts is represented graphically by the proportion of cohort participants with a peak systolic velocity above 125 cm/s. (A) In the Cardiovascular Health Study, the prevalence of disease ( orange portion to the right of the curve ) is about 10%. (B) In the Multi-Ethnic Study of Atherosclerosis, it is closer to 5%.

Estimating the accuracy of carotid artery Doppler ultrasound

Accuracy of Doppler ultrasound for detecting the presence of a carotid artery stenosis above a certain threshold is measured by sensitivity and specificity values using the true positives, true negatives, false positives, and false negatives ( Table 33.3 ). Additional metrics such as the negative and positive predictive values are also very important when considering the value of a screening examination. A screening carotid Doppler examination has to be as sensitive as possible when compared with the gold standard measurement using arteriography ( Fig. 33.3 ). Although we would like to make sure that the individuals we classify as negative are without significant stenosis, we need to set a Doppler velocity threshold low enough so that all, or almost all, individuals with significant disease are identified. However, by setting a low velocity threshold, we detect not only individuals with significant stenosis but also individuals without disease, and the false positive rate increases. This leads to a low positive predictive value and a high negative predictive value ( Table 33.4 ). This is the basic dilemma of any screening test: the sensitivity has to be set very high. Therefore to screen a population for asymptomatic carotid artery stenosis, the Doppler velocity threshold for a given degree of stenosis is set lower than normal, and many individuals are misclassified as having a significant stenosis ( Fig. 33.4 ). The overall performance of this process is also affected by disease prevalence. With a low disease prevalence, more individuals are screened and more false positives occur.

TABLE 33.3

Key Parameters for a Screening Test.

	Disease Present	Disease Absent
Test positive for disease	a	b
Test negative for disease	c	d
Total	a + c	b + d

True positives: a

True negatives: d

False positives: b

False negatives: c

Sensitivity: a / (a + c)

Specificity: d / (b + d)

Disease prevalence: (a + c) / (a + c + b + d)

Positive predictive value: a / (a + b)

Negative predictive value: d / (c + d)

FIG. 33.3, The limitations of using carotid artery Doppler peak systolic velocity when screening for stenosis ≥50% is shown here by plotting the source data shown in Fig. 33.1 . (A) In the ideal situation, the distribution of Doppler velocities for stenosis ≥50% ( blue to the right ) would not overlap with carotid arteries with less than 50% stenosis. (B) The reality is shown here: there is marked overlap of the Doppler velocities between carotid stenosis of less than 50% ( orange ) and ≥50% ( blue ). (C) The use of a peak systolic velocity cut-point of 125 cm/s creates true negatives and quite a large number of false positives. (D) Conversely, although many of the lesions above 50% stenosis are detected (true positives), there are still a few false negatives.

TABLE 33.4

Estimated Rates of Detection of Disease and False Positives for a High Accuracy Diagnostic Test. ^a ^, ^b

Prevalence	Sensitivity/Specificity	True Positive	False Positives	Positive Predictive Value	Negative Predictive Value
10%	90%/90%	180	162	52.6%	98.8%
	95%/85%	190	270	41.3%	99.4%
5%	90%/90%	90	171	34.5%	99.4%
	95%/85%	95	285	25%	99.7%

a Calculations are based on 2000 individuals being screened with disease prevalence of 10% and 5%.

b Calculations are based on equations shown in Table 33.3 . Estimates of the true positives and false positives can be extrapolated for larger populations by multiplying the numbers in these columns by (number in population/2000).

FIG. 33.4, The effect of shifting the Doppler velocity cut-point on the diagnostic accuracy of Doppler ultrasound is shown here. The curve to the left represents lesions of less than 50% stenosis ( orange ) and those on the right ≥50% stenosis ( blue ). (A) The false negatives and false positives are shown for a cut-point of 125 cm/s. Diagnostic performance favors high sensitivity (few false negatives) at the cost of many false positives. (B) The effect of shifting the velocity cut-point to 230 cm/s is to decrease the false positives at the cost of decreasing sensitivity (increasing the false negatives).

Doppler ultrasound in carotid endarterectomy trials of asymptomatic patients

Diagnostic performance

Multicenter trials have used Doppler velocity measurements to identify asymptomatic individuals with significant carotid artery stenosis, for example ≥60% diameter narrowing in the Asymptomatic Carotid Atherosclerosis Study (ACAS) or ≥75% stenosis in the European Asymptomatic Carotid Surgery Trial (ACST). The ACAS investigators used carotid Doppler ultrasound as a screening test but with the intent of ensuring that almost all individuals who went on to carotid arteriography and surgery would have a lesion of at least 60% in their carotid artery. For this reason, the selected Doppler velocity threshold was set to a high enough value so that 95% of selected individuals would have a lesion causing a diameter narrowing of 60% or more (i.e., a high velocity threshold with few false positives) (see Fig. 33.4 as an example). This approach yielded a high positive predictive value and also resulted in a low negative predictive value. In essence, many individuals who probably had a carotid artery stenosis above 60% were missed (see Fig. 33.4 ), but 92% of individuals who underwent arteriography had a ≥60% internal carotid artery stenosis.

The ACAS Trial gives insights into the use of carotid Doppler ultrasound as a screening tool. On the technical side, lessons to be learned from this study are the need for adherence to a quality control process, adherence to strict protocols, and selection of an appropriate ultrasound device.

Although the overall sensitivity of carotid Doppler ultrasound could not be measured in ACAS, the overall specificity of carotid ultrasound was above 97%. Carotid ultrasound was, however, used according to a very strict protocol. Qualifying centers needed to show a strong correlation between Doppler measurements and the results of carotid arteriography. Marked variations between centers and outlier centers with poor accuracy of carotid Doppler improved with new ultrasound equipment and a standardized imaging protocol. The success of carotid ultrasound in ACAS was based on the use of a standard imaging protocol, a certification program for both sonographers and vascular laboratories, and the implementation of a quality assurance program supervised by a central coordinating center.

Effect of ultrasound devices

Differences in imaging devices or imaging protocols probably affected the diagnostic performance of Doppler ultrasound in ACAS and are therefore likely to affect any screening process that looks at detecting significant carotid artery stenosis in the general and high-risk populations. The variability of carotid Doppler ultrasound is measurable at the level of individual laboratories and for different imaging devices. These observations confirmed the observations made by ACAS. Despite this variability, carotid Doppler ultrasound can still perform well as a screening tool. The European ACST used locally derived parameters to define percent stenosis by carotid ultrasound and achieved very similar outcome results to those of the ACAS study.

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