Noninvasive Diagnosis of Upper Extremity Arterial Disease



Noninvasive Diagnosis of Upper Extremity Arterial Disease


Gregory L. Moneta

Molly Zaccardi



Symptomatic arterial disease of the upper extremity accounts for only about 5% of all cases of extremity ischemia. Unlike the lower extremity, where atherosclerosis is by far the most common pathology, ischemia in the upper extremity may be caused by a variety of local and systemic conditions, and the diagnosis of upper extremity arterial diseases is therefore often complex. A complete history and physical examination, plain x-rays of the neck and shoulder regions, blood tests, and noninvasive and invasive examinations of the upper extremity arteries may all be required.

Surgical intervention is rarely necessary for most etiologies of upper extremity arterial disease. Arteriography is now infrequently required for the diagnosis of upper extremity ischemia, and the anatomic and physiologic information needed for diagnosis can usually be obtained with noninvasive diagnostic testing. Noninvasive vascular laboratory testing for upper extremity arterial disease includes segmental arm pressures, digit pressure measurements and digital plethysmography, and testing for cold-induced vasospasm. Duplex scanning plays somewhat less of a role in the diagnosis of upper extremity ischemia compared to its importance in the evaluation of lower extremity ischemia but is still important in cases amenable to surgical treatment.


CLINICAL PRESENTATION

Raynaud’s syndrome is a frequent manifestation of upper extremity arterial disease. Raynaud’s syndrome is characterized by episodic attacks of digital artery spasm in response to cold exposure or emotional stimuli. Classic attacks consist of intense pallor of the fingers or distal hand followed by cyanosis and finally rubor upon rewarming. Full recovery requires 15 to 45 minutes after the inciting stimulus is removed (Fig. 14.1). These classic “tricolor” attacks do not occur in all patients. Some patients develop only pallor or cyanosis during the episode, and others complain of cold hands without digit color changes but have abnormal findings on noninvasive testing that are identical to patients with classic digit color changes.

Patients with Raynaud’s syndrome are traditionally divided into two groups.1 The term Raynaud’s disease is used to describe a benign idiopathic form of intermittent digital ischemia occurring in the absence of known associated diseases. Raynaud’s phenomenon is used to describe similar symptoms occurring in association with a variety of underlying disease states. It is well recognized that the presence of an underlying disease may not be established at the time a patient presents with Raynaud’s syndrome.2 Therefore, the distinction between Raynaud’s disease and Raynaud’s phenomenon is somewhat artificial and uncertain. The clinical manifestations of Raynaud’s syndrome should be considered as symptoms requiring a diagnosis rather than a diagnosis in itself. In most cases, the diagnosis will be episodic vasospasm without a known associated underlying condition. In cool, damp climates, 6% to 20% of the population, particularly young females, will report symptoms of Raynaud’s syndrome.

In about 5% of cases, an underlying condition will be discovered in association with Raynaud’s syndrome. The vascular laboratory can play an important role in separating benign episodic vasospasm (Raynaud’s disease) from vasospasm associated with serious underlying conditions requiring medical or surgical management (Raynaud’s phenomenon).4,5 With the exception of vasospastic episodes induced by vasopressor medications or ergot, vasospasm alone very rarely results in tissue loss or ulceration. The presence of ulceration or digital gangrene should trigger a workup to confirm the presence of digital artery occlusive disease and an associated condition (Fig. 14.2).




NONINVASIVE DIAGNOSTIC TECHNIQUES

Noninvasive vascular laboratory testing of the upper extremity arteries begins with a physical examination. The fingers should be carefully inspected for the presence of ulcers. Hyperkeratotic areas are suggestive of healed ulcers. The hands and fingers should also be examined for telangiectasias, skin thinning, tightening, or sclerodactyly, indicating an associated autoimmune disease. Signs and symptoms of nerve compression syndrome should also be sought. Carpal tunnel syndrome is seen in about 15% of Raynaud’s patients.7 While the physical examination is frequently completely normal in patients with Raynaud’s syndrome, a complete pulse examination of all extremities must be performed with attention to the strength and quality of pulses as well as the presence of aneurysms or bruits.


Segmental Arm Pressures

No special patient preparation is required for measurement of segmental arm pressures. Upper extremity segmental pressures are obtained by measuring systolic blood pressure with pneumatic cuffs placed above the elbow, below the elbow, and above the wrist while insonating the radial or ulnar artery at the wrist with a continuous-wave Doppler. Doppler-derived waveforms or plethysmographic waveforms can also be recorded at the different levels. Abnormal waveforms or pressures indicate arterial occlusive disease proximal to the wrist.

A 12-cm-wide blood pressure cuff is usually sufficient for measuring the systolic pressure above the elbow (brachial artery), whereas 10-cm-wide cuffs are used below the elbow and above the wrist (radial and ulnar arteries). However, in general, cuff width should be at least 50% greater than the diameter of the limb in which pressure is being measured. The use of smaller cuffs results in the recording of falsely high pressures. Normally, the gradient between adjacent levels is minimal, and a normal wrist-to-brachial blood pressure ratio is 1.0. If the systolic blood pressure difference between the two arms is more than 15 mm Hg, it is likely that there is a stenosis or occlusion somewhere on the side with the lower pressure. Abnormal Doppler waveforms and decreased pressures at the above-elbow cuff site indicate axillary, subclavian, or brachiocephalic arterial occlusive disease. Similarly, abnormalities at the below-elbow and above-wrist sites indicate brachial and
proximal ulnar/radial arterial occlusive disease, respectively. If the blood pressure difference is more than 15 mm Hg between adjacent levels, or between the radial and ulnar arteries, it is likely due to a stenosis or occlusion (Fig. 14.4).








TABLE 14.1 DISEASES ASSOCIATED WITH INTRINSIC DIGITAL ARTERY OCCLUSIONS



































DISEASE TYPE


EXAMPLE


Connective tissue disease


Scleroderma, CREST syndrome, systemic lupus erythematosus, rheumatoid arthritis, Sjögren’s syndrome, mixed connective tissue disease, dermatomyositis, small and medium vessel vasculitis


Atherosclerosis and occlusive arterial disease


Atherosclerosis obliterans, atheroembolism, diabetic distal arterial disease, thromboangiitis obliterans (Buerger’s disease)


Thromboembolism


Cardiac embolism, arterial embolism, paradoxical embolism


Large vessel vasculitis


Takayasu’s arteritis, extracranial temporal arteritis


Dynamic entrapment


Arterial thoracic outlet syndrome


Occupational arterial trauma


Hypothenar hammer syndrome, vibration-induced Raynaud’s syndrome


Drug-induced vasospasm


β-Blockers, vasopressors, epinephrine, ergot, cocaine, amphetamines, vinblastine/bleomycin


Infections


Parvovirus, hepatitis B and C antigenemia, sepsis/disseminated intravascular coagulation


Malignancy Hematologic


Multiple myeloma, leukemia, adenocarcinoma, astrocytoma Polycythemia vera, thrombocytosis, cold agglutinins, cryoglobulinemia


CREST, calcinosis cutis, Raynaud’s phenomenon, esophageal dysfunction, sclerodactyly, telangiectasia.



Digit Pressures and Plethysmography

It is important to measure and record finger temperature before performing digital plethysmography and obtaining finger blood pressures. If the finger temperature is less than 28°C to 30°C, false-positive results may occur secondary to cold-induced vasospasm. Hand or whole-body warming should be performed in patients with low finger temperatures. The technologist should record the finger temperatures to ensure the interpreting physician that the chances of vasospasm have been minimized.

Photoplethysmography (PPG) or strain-gauge plethysmography can be used to measure digit blood pressure5 and obtain volume pulse waveforms. Alternating current ([AC]-coupled) PPG is preferred because the equipment is easier to use and more durable. An additional advantage of PPG is that it is possible to record the volume pulses from the tips of the digits. This may be useful in documenting obstruction localized to the digital arteries.

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Sep 23, 2016 | Posted by in CARDIOLOGY | Comments Off on Noninvasive Diagnosis of Upper Extremity Arterial Disease

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