Edema: Diagnosis and Management

Am Fam Physician. 2013 Jul 15;88(2):102-110.

  Patient information: A handout on this topic is available at http://familydoctor.org/familydoctor/en/diseases-conditions/edema.html.

  This version of the article contains supplemental content.

This clinical content conforms to AAFP criteria for continuing medical education (CME). See the CME Quiz.

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Edema is an accumulation of fluid in the interstitial space that occurs as the capillary filtration exceeds the limits of lymphatic drainage, producing noticeable clinical signs and symptoms. The rapid development of generalized pitting edema associated with systemic disease requires timely diagnosis and management. The chronic accumulation of edema in one or both lower extremities often indicates venous insufficiency, especially in the presence of dependent edema and hemosiderin deposition. Skin care is crucial in preventing skin breakdown and venous ulcers. Eczematous (stasis) dermatitis can be managed with emollients and topical steroid creams. Patients who have had deep venous thrombosis should wear compression stockings to prevent postthrombotic syndrome. If clinical suspicion for deep venous thrombosis remains high after negative results are noted on duplex ultrasonography, further investigation may include magnetic resonance venography to rule out pelvic or thigh proximal venous thrombosis or compression. Obstructive sleep apnea may cause bilateral leg edema even in the absence of pulmonary hypertension. Brawny, nonpitting skin with edema characterizes lymphedema, which can present in one or both lower extremities. Possible secondary causes of lymphedema include tumor, trauma, previous pelvic surgery, inguinal lymphadenectomy, and previous radiation therapy. Use of pneumatic compression devices or compression stockings may be helpful in these cases.

Edema is an accumulation of fluid in the intercellular tissue that results from an abnormal expansion in interstitial fluid volume. The fluid between the interstitial and intravascular spaces is regulated by the capillary hydrostatic pressure gradient and the oncotic pressure gradient across the capillary.13  The accumulation of fluid occurs when local or systemic conditions disrupt this equilibrium (Table 1113), leading to increased capillary hydrostatic pressure, increased plasma volume, decreased plasma oncotic pressure (hypoalbuminemia), increased capillary permeability, or lymphatic obstruction.

SORT: KEY RECOMMENDATIONS FOR PRACTICE

Clinical recommendation Evidence rating References

Magnetic resonance venography of the lower extremity and pelvis should be obtained in patients with unilateral left leg swelling and negative results on duplex ultrasonography if there is high clinical suspicion for deep venous thrombosis.

C

22, 23

Echocardiography should be performed in patients with obesity, obstructive sleep apnea, and edema to evaluate pulmonary arterial pressures.

C

27, 28

Ankle-brachial index should be measured in patients with chronic venous insufficiency and cardiovascular risk factors before initiation of compression therapy, which is contraindicated in peripheral arterial disease.

C

30, 31

Daily hydration with emollients and short courses of topical steroid creams for severely inflamed skin should be used to treat eczematous (stasis) dermatitis associated with chronic venous insufficiency.

C

36

Pneumatic compression devices should be used in conjunction with standard therapy in patients with lymphedema.

C

11, 39, 40

Compression stockings should be used in patients following deep venous thrombosis to prevent postthrombotic syndrome.

A

4143


A = consistent, good-quality patient-oriented evidence; B = inconsistent or limited-quality patient-oriented evidence; C = consensus, disease-oriented evidence, usual practice, expert opinion, or case series. For information about the SORT evidence rating system, go to http://www.aafp.org/afpsort.

SORT: KEY RECOMMENDATIONS FOR PRACTICE

View Table

SORT: KEY RECOMMENDATIONS FOR PRACTICE

Clinical recommendation Evidence rating References

Magnetic resonance venography of the lower extremity and pelvis should be obtained in patients with unilateral left leg swelling and negative results on duplex ultrasonography if there is high clinical suspicion for deep venous thrombosis.

C

22, 23

Echocardiography should be performed in patients with obesity, obstructive sleep apnea, and edema to evaluate pulmonary arterial pressures.

C

27, 28

Ankle-brachial index should be measured in patients with chronic venous insufficiency and cardiovascular risk factors before initiation of compression therapy, which is contraindicated in peripheral arterial disease.

C

30, 31

Daily hydration with emollients and short courses of topical steroid creams for severely inflamed skin should be used to treat eczematous (stasis) dermatitis associated with chronic venous insufficiency.

C

36

Pneumatic compression devices should be used in conjunction with standard therapy in patients with lymphedema.

C

11, 39, 40

Compression stockings should be used in patients following deep venous thrombosis to prevent postthrombotic syndrome.

A

4143


A = consistent, good-quality patient-oriented evidence; B = inconsistent or limited-quality patient-oriented evidence; C = consensus, disease-oriented evidence, usual practice, expert opinion, or case series. For information about the SORT evidence rating system, go to http://www.aafp.org/afpsort.

Table 1.

Systemic and Localized Causes of Edema

Cause Mechanism of action

Systemic

Allergic reaction, urticaria, and angioedema

Increased capillary permeability

Cardiac disease

Increased capillary permeability from systemic venous hypertension; increased plasma volume

Hepatic disease

Increased capillary permeability from systemic venous hypertension; decreased plasma oncotic pressure from reduced protein synthesis

Malabsorption/protein-calorie malnutrition

Reduced protein synthesis leading to decreased plasma oncotic pressure

Obstructive sleep apnea

Pulmonary hypertension resulting in increased capillary hydrostatic pressure

Pregnancy and premenstrual edema

Increased plasma volume

Renal disease

Increased plasma volume; decreased plasma oncotic pressure from protein loss

Localized

Cellulitis

Increased capillary permeability

Chronic venous insufficiency

Increased capillary permeability caused by local venous hypertension

Compartment syndrome

Increased capillary permeability caused by local venous hypertension

Complex regional pain syndrome type 1 (reflex sympathetic dystrophy)

Neurogenically mediated increased capillary permeability

Deep venous thrombosis

Increased capillary permeability

Iliac vein obstruction

Increased capillary permeability caused by local venous hypertension

Lipedema

Accumulation of fluid in adipose tissue

Lymphedema

Lymphatic obstruction

Primary: congenital lymphedema, lymphedema praecox, lymphedema tarda

Secondary: from axillary lymph node dissection, surgery (e.g., coronary artery bypass graft, inguinal lymphadenectomy), trauma, radiation, tumor, filariasis

May-Thurner syndrome (compression of left iliac vein by right iliac artery)

Increased capillary permeability caused by local venous hypertension from compression


Information from references 1 through 13.

Table 1.   Systemic and Localized Causes of Edema

View Table

Table 1.

Systemic and Localized Causes of Edema

Cause Mechanism of action

Systemic

Allergic reaction, urticaria, and angioedema

Increased capillary permeability

Cardiac disease

Increased capillary permeability from systemic venous hypertension; increased plasma volume

Hepatic disease

Increased capillary permeability from systemic venous hypertension; decreased plasma oncotic pressure from reduced protein synthesis

Malabsorption/protein-calorie malnutrition

Reduced protein synthesis leading to decreased plasma oncotic pressure

Obstructive sleep apnea

Pulmonary hypertension resulting in increased capillary hydrostatic pressure

Pregnancy and premenstrual edema

Increased plasma volume

Renal disease

Increased plasma volume; decreased plasma oncotic pressure from protein loss

Localized

Cellulitis

Increased capillary permeability

Chronic venous insufficiency

Increased capillary permeability caused by local venous hypertension

Compartment syndrome

Increased capillary permeability caused by local venous hypertension

Complex regional pain syndrome type 1 (reflex sympathetic dystrophy)

Neurogenically mediated increased capillary permeability

Deep venous thrombosis

Increased capillary permeability

Iliac vein obstruction

Increased capillary permeability caused by local venous hypertension

Lipedema

Accumulation of fluid in adipose tissue

Lymphedema

Lymphatic obstruction

Primary: congenital lymphedema, lymphedema praecox, lymphedema tarda

Secondary: from axillary lymph node dissection, surgery (e.g., coronary artery bypass graft, inguinal lymphadenectomy), trauma, radiation, tumor, filariasis

May-Thurner syndrome (compression of left iliac vein by right iliac artery)

Increased capillary permeability caused by local venous hypertension from compression


Information from references 1 through 13.

Assessment of Edema

HISTORY

The history should include the timing of the edema, whether it changes with position, and if it is unilateral or bilateral, as well as a medication history and an assessment for systemic diseases (Table 2). Acute swelling of a limb over a period of less than 72 hours is more characteristic of deep venous thrombosis (DVT), cellulitis, ruptured popliteal cyst, acute compartment syndrome from trauma, or recent initiation of calcium channel blockers (Figures 1 and 2). The chronic accumulation of more generalized edema is due to the onset or exacerbation of chronic systemic conditions, such as congestive heart failure (CHF), renal disease, or hepatic disease.4,5

Table 2.

Diagnosis and Management of Common Causes of Localized Edema

Etiology Onset and location Examination findings Evaluation methods Treatment

Unilateral predominance

Chronic venous insufficiency

Onset: chronic; begins in middle to older age

Location: lower extremities; bilateral distribution in later stages

Soft, pitting edema with reddish-hued skin; predilection for medial ankle/calf

Associated findings: venous ulcerations over medial malleolus; weeping erosions

Duplex ultrasonography

Ankle-brachial index to evaluate for arterial insufficiency

Compression stockings

Pneumatic compression device if stockings are contraindicated

Horse chestnut seed extract

Skin care (e.g., emollients, topical steroids)

Complex regional pain syndrome type 1 (reflex sympathetic dystrophy)

Onset: chronic; following trauma or other inciting event

Location: upper or lower extremities; contralateral limb at risk regardless of trauma

Soft tissue edema distal to affected limb

Associated findings: (early) warm, tender skin with diaphoresis; (late) thin, shiny skin with atrophic changes

History and examination

Radiography

Three-phase bone scintigraphy

Magnetic resonance imaging

Systemic steroids

Topical dimethyl sulfoxide solution

Physical therapy

Tricyclic antidepressants

Calcium channel blockers

DVT

Onset: acute

Location: upper or lower extremities

Pitting edema with tenderness, with or without erythema; positive Homans sign

d-dimer assay

Duplex ultrasonography

Magnetic resonance venography to rule out pelvic or thigh DVT (if clinical suspicion is high), or extrinsic venous compression (May-Thurner syndrome in patients with unexplained left-sided DVT)

Consider hypercoagulability workup

Anticoagulation therapy

Compression stockings to prevent postthrombotic syndrome

Thrombolysis in select patients

Lymphedema

Onset: chronic; insidious; often following lymphatic obstruction from trauma or surgery

Location: upper or lower extremities; bilateral in 30% of patients

Early: dough-like skin; pitting

Late: thickened, verrucous, fibrotic, hyperkeratotic skin

Associated findings: inability to tent skin over second digit, swelling of dorsum of foot with squared off digits, painless heaviness in extremity

Clinical diagnosis

Lymphoscintigraphy

T1-weighted magnetic resonance lymphangiography

Complex decongestive physiotherapy

Compression stockings with adjuvant pneumatic compression devices

Skin care

Surgery in limited cases

Bilateral predominance

Lipedema

Onset: chronic; begins around or after puberty

Location: predominantly lower extremities; involves thighs, legs, buttocks; spares feet, ankles, and upper torso

Nonpitting edema; increased distribution of soft, adipose tissue

Associated findings: medial thigh and tibial tenderness; fat pad anterior to lateral malleoli

Clinical diagnosis

No effective treatment

Weight loss does not improve edema

Medication-induced edema

Onset: weeks after initiation of medication; resolves within days of stopping offending medication

Location: lower extremities

Soft, pitting edema

Clinical history suggesting recent initiation of offending medication

Cessation of medication

Obstructive sleep apnea

Onset: chronic

Location: lower extremities

Mild, pitting edema

Associated findings: daytime fatigue, snoring, obesity

Suggestive clinical history

Polysomnography

Echocardiography

Positive pressure ventilation

Treatment of pulmonary hypertension if suggested on echocardiography


DVT = deep venous thrombosis.

Table 2.   Diagnosis and Management of Common Causes of Localized Edema

View Table

Table 2.

Diagnosis and Management of Common Causes of Localized Edema

Etiology Onset and location Examination findings Evaluation methods Treatment

Unilateral predominance

Chronic venous insufficiency

Onset: chronic; begins in middle to older age

Location: lower extremities; bilateral distribution in later stages

Soft, pitting edema with reddish-hued skin; predilection for medial ankle/calf

Associated findings: venous ulcerations over medial malleolus; weeping erosions

Duplex ultrasonography

Ankle-brachial index to evaluate for arterial insufficiency

Compression stockings

Pneumatic compression device if stockings are contraindicated

Horse chestnut seed extract

Skin care (e.g., emollients, topical steroids)

Complex regional pain syndrome type 1 (reflex sympathetic dystrophy)

Onset: chronic; following trauma or other inciting event

Location: upper or lower extremities; contralateral limb at risk regardless of trauma

Soft tissue edema distal to affected limb

Associated findings: (early) warm, tender skin with diaphoresis; (late) thin, shiny skin with atrophic changes

History and examination

Radiography

Three-phase bone scintigraphy

Magnetic resonance imaging

Systemic steroids

Topical dimethyl sulfoxide solution

Physical therapy

Tricyclic antidepressants

Calcium channel blockers

DVT

Onset: acute

Location: upper or lower extremities

Pitting edema with tenderness, with or without erythema; positive Homans sign

d-dimer assay

Duplex ultrasonography

Magnetic resonance venography to rule out pelvic or thigh DVT (if clinical suspicion is high), or extrinsic venous compression (May-Thurner syndrome in patients with unexplained left-sided DVT)

Consider hypercoagulability workup

Anticoagulation therapy

Compression stockings to prevent postthrombotic syndrome

Thrombolysis in select patients

Lymphedema

Onset: chronic; insidious; often following lymphatic obstruction from trauma or surgery

Location: upper or lower extremities; bilateral in 30% of patients

Early: dough-like skin; pitting

Late: thickened, verrucous, fibrotic, hyperkeratotic skin

Associated findings: inability to tent skin over second digit, swelling of dorsum of foot with squared off digits, painless heaviness in extremity

Clinical diagnosis

Lymphoscintigraphy

T1-weighted magnetic resonance lymphangiography

Complex decongestive physiotherapy

Compression stockings with adjuvant pneumatic compression devices

Skin care

Surgery in limited cases

Bilateral predominance

Lipedema

Onset: chronic; begins around or after puberty

Location: predominantly lower extremities; involves thighs, legs, buttocks; spares feet, ankles, and upper torso

Nonpitting edema; increased distribution of soft, adipose tissue

Associated findings: medial thigh and tibial tenderness; fat pad anterior to lateral malleoli

Clinical diagnosis

No effective treatment

Weight loss does not improve edema

Medication-induced edema

Onset: weeks after initiation of medication; resolves within days of stopping offending medication

Location: lower extremities

Soft, pitting edema

Clinical history suggesting recent initiation of offending medication

Cessation of medication

Obstructive sleep apnea

Onset: chronic

Location: lower extremities

Mild, pitting edema

Associated findings: daytime fatigue, snoring, obesity

Suggestive clinical history

Polysomnography

Echocardiography

Positive pressure ventilation

Treatment of pulmonary hypertension if suggested on echocardiography


DVT = deep venous thrombosis.

Diagnostic Approach to Unilateral Lower Extremity Edema

Figure 1.

Algorithm for the diagnosis of unilateral lower extremity edema. (DVT = deep venous thrombosis.)

View Large

Diagnostic Approach to Unilateral Lower Extremity Edema


Figure 1.

Algorithm for the diagnosis of unilateral lower extremity edema. (DVT = deep venous thrombosis.)

Diagnostic Approach to Unilateral Lower Extremity Edema


Figure 1.

Algorithm for the diagnosis of unilateral lower extremity edema. (DVT = deep venous thrombosis.)

Diagnostic Approach to Bilateral Lower Extremity Edema or Anasarca

Figure 2.

Algorithm for the diagnosis of bilateral lower extremity edema or anasarca.

View Large

Diagnostic Approach to Bilateral Lower Extremity Edema or Anasarca


Figure 2.

Algorithm for the diagnosis of bilateral lower extremity edema or anasarca.

Diagnostic Approach to Bilateral Lower Extremity Edema or Anasarca


Figure 2.

Algorithm for the diagnosis of bilateral lower extremity edema or anasarca.

Dependent edema caused by venous insufficiency is more likely to improve with elevation and worsen with dependency.5,14 Edema associated with decreased plasma oncotic pressure (e.g., malabsorption, liver failure, nephrotic syndrome) does not change with dependency.

Unilateral swelling from compression or compromise of venous or lymphatic drainage can result from DVT, venous insufficiency, venous obstruction by tumor (e.g., tumor obstruction of the iliac vein), lymphatic obstruction (e.g., from a pelvic tumor or lymphoma), or lymphatic destruction (e.g., congenital vs. secondary from a tumor, radiation, or filariasis). Bilateral or generalized swelling suggests a systemic cause, such as CHF (especially right-sided), pulmonary hypertension, chronic renal or hepatic disease (causing hypoalbuminemia), protein-losing enteropathies, or severe malnutrition.1,4,5

Edema can be an adverse effect of certain medications (Table 315). The mechanism often includes the retention of salt and water with increased capillary hydrostatic pressure. Diuretic use may cause volume depletion and reflex stimulation of the reninangiotensin system.

Table 3.

Medications Commonly Associated with Edema

Class Specific medications

Antidepressants

Monoamine oxidase inhibitors, trazodone

Antihypertensives

Beta-adrenergic blockers, calcium channel blockers, clonidine (Catapres), hydralazine, methyldopa, minoxidil

Antivirals

Acyclovir (Zovirax)

Chemotherapeutics

Cyclophosphamide, cyclosporine (Sandimmune), cytosine arabinoside, mithramycin

Cytokines

Granulocyte colony-stimulating factor, granulocyte-macrophage colony-stimulating factor, interferon alfa, interleukin-2, interleukin-4

Hormones

Androgen, corticosteroids, estrogen, progesterone, testosterone

Nonsteroidal anti- inflammatory drugs

Celecoxib (Celebrex), ibuprofen


Information from references 1 through 5.

Table 3.   Medications Commonly Associated with Edema

View Table

Table 3.

Medications Commonly Associated with Edema

Class Specific medications

Antidepressants

Monoamine oxidase inhibitors, trazodone

Antihypertensives

Beta-adrenergic blockers, calcium channel blockers, clonidine (Catapres), hydralazine, methyldopa, minoxidil

Antivirals

Acyclovir (Zovirax)

Chemotherapeutics

Cyclophosphamide, cyclosporine (Sandimmune), cytosine arabinoside, mithramycin

Cytokines

Granulocyte colony-stimulating factor, granulocyte-macrophage colony-stimulating factor, interferon alfa, interleukin-2, interleukin-4

Hormones

Androgen, corticosteroids, estrogen, progesterone, testosterone

Nonsteroidal anti- inflammatory drugs

Celecoxib (Celebrex), ibuprofen


Information from references 1 through 5.

The history should also include questions about cardiac, renal, thyroid, or hepatic disease. Graves disease can lead to pretibial myxedema, whereas hypothyroidism can cause generalized myxedema. Although considered a diagnosis of exclusion, obstructive sleep apnea has been shown to cause edema. One study evaluated the apnea-hypopnea index in patients with obstructive sleep apnea and found that even when adjusted for age, body mass index, and the presence of hypertension and diabetes mellitus, the index was higher in patients who had edema.15

PHYSICAL EXAMINATION

The physical examination should assess for systemic causes of edema, such as heart failure (e.g., jugular venous distention, crackles), renal disease (e.g., proteinuria, oliguria), hepatic disease (e.g., jaundice, ascites, asterixis), or thyroid disease (e.g., exophthalmos, tremor, weight loss). Edema should also be evaluated for pitting, tenderness, and skin changes.

Pitting describes an indentation that remains in the edematous area after pressure is applied (Figure 3). This occurs when fluid in the interstitial space has a low concentration of protein, which is associated with decreased plasma oncotic pressure and disorders caused by increased capillary pressure (e.g., DVT, CHF, iliac vein compression).4,16 The physician should describe the location, timing, and extent of the pitting to determine treatment response. Lower extremity examination should focus on the medial malleolus, the bony portion of the tibia, and the dorsum of the foot. Pitting edema also occurs in the early stages of lymphedema because of an influx of protein-rich fluid into the interstitium, before fibrosis of the subcutaneous tissue; therefore, its presence should not exclude the diagnosis of lymphedema.6,7 Tenderness to palpation over the edematous area is associated with DVT and complex regional pain syndrome type 1 (i.e., reflex sympathetic dystrophy). Conversely, lymphedema generally does not elicit pain with palpation.

Figure 3.

Pitting edema, bilateral, as observed in a patient with congestive heart failure.

View Large


Figure 3.

Pitting edema, bilateral, as observed in a patient with congestive heart failure.


Figure 3.

Pitting edema, bilateral, as observed in a patient with congestive heart failure.

Changes in skin temperature, color, and texture provide clues to the cause of edema. For example, acute DVT and cellulitis (Figure 4) may produce increased warmth over the affected area. Because of the deposition of hemosiderin, chronic venous insufficiency is often associated with skin that has a brawny, reddish hue and commonly involves the medial malleolus4,5,8 (eFigure A). As venous insufficiency progresses, it can result in lipodermatosclerosis (Figure 5), which is associated with marked sclerotic and hyperpigmented tissue, and characterized by fibrosis and hemosiderin deposition that can lead to venous ulcers over the medial malleolus. These ulcers may progress to deep, weeping erosions. Myxedema from hypothyroidism presents with a generalized dry, thick skin with nonpitting periorbital edema and yellow to orange skin discoloration over the knees, elbows, palms, and soles. Localized pretibial myxedema may be caused by Graves disease (eFigure B). In the late stages of complex regional pain syndrome, the skin may appear shiny with atrophic changes. In the early stages of lymphedema, the skin has a doughy appearance, whereas in the later stages, it becomes fibrotic, thickened, and verrucous (eFigure C).

Figure 4.

Acute deep venous thrombosis with overlying cellulitis.

View Large


Figure 4.

Acute deep venous thrombosis with overlying cellulitis.


Figure 4.

Acute deep venous thrombosis with overlying cellulitis.

eFigure A.

Venous insufficiency with venous stasis ulcer over the medial malleolus. Note the yellow-brown hemosiderin deposition.

View Large


eFigure A.

Venous insufficiency with venous stasis ulcer over the medial malleolus. Note the yellow-brown hemosiderin deposition.


eFigure A.

Venous insufficiency with venous stasis ulcer over the medial malleolus. Note the yellow-brown hemosiderin deposition.

Figure 5.

Lipodermatosclerosis from chronic venous insufficiency associated with marked sclerotic and hyperpigmented tissue.

View Large


Figure 5.

Lipodermatosclerosis from chronic venous insufficiency associated with marked sclerotic and hyperpigmented tissue.


Figure 5.

Lipodermatosclerosis from chronic venous insufficiency associated with marked sclerotic and hyperpigmented tissue.

eFigure B.

Pretibial myxedema causing a peau d'orange appearance in a patient with Graves disease.

View Large


eFigure B.

Pretibial myxedema causing a peau d'orange appearance in a patient with Graves disease.


eFigure B.

Pretibial myxedema causing a peau d'orange appearance in a patient with Graves disease.

eFigure C.

Long-standing lymphedema with thickened, verrucous skin.

View Large


eFigure C.

Long-standing lymphedema with thickened, verrucous skin.


eFigure C.

Long-standing lymphedema with thickened, verrucous skin.

Examination of the feet is important in lower extremity edema. In patients with lymphedema, there is an inability to tent the skin of the dorsum of the second toe using a pincer grasp (Kaposi-Stemmer sign)7,911 (eFigure D). In patients with lipedema, which is a pathologic accumulation of adipose tissue in the extremities, the feet are generally spared, although the ankles often have prominent malleolar fat pads.12 Lipedema can also involve the upper extremities.

eFigure D.

Failure to tent the skin overlying the dorsum of the second toe using a pincer grasp (Kaposi-Stemmer sign) in a patient with lymphedema.

View Large


eFigure D.

Failure to tent the skin overlying the dorsum of the second toe using a pincer grasp (Kaposi-Stemmer sign) in a patient with lymphedema.


eFigure D.

Failure to tent the skin overlying the dorsum of the second toe using a pincer grasp (Kaposi-Stemmer sign) in a patient with lymphedema.

DIAGNOSTIC TESTING

Recommendations for diagnostic testing are listed in Table 2. The following laboratory tests are useful for diagnosing systemic causes of edema: brain natriuretic peptide measurement (for CHF), creatinine measurement and urinalysis (for renal disease), and hepatic enzyme and albumin measurement (for hepatic disease). In patients who present with acute onset of unilateral upper or lower extremity swelling, a d-dimer enzyme-linked immunosorbent assay can rule out DVT in low-risk patients. However, this test has a low specificity, and d-dimer concentrations may be elevated in the absence of thrombosis.13,17,18

ULTRASONOGRAPHY

Venous ultrasonography is the imaging modality of choice in the evaluation of suspected DVT. Compression ultrasonography with or without Doppler waveform analysis has a high sensitivity (95%) and specificity (96%) for proximal thrombosis; however, the sensitivity is lower for calf veins (73%).13,19,20 Duplex ultrasonography can also be used to confirm the diagnosis of chronic venous insufficiency.

LYMPHOSCINTIGRAPHY

Lymph flow cannot be detected with ultrasonography. Therefore, indirect radionuclide lymphoscintigraphy, which shows absent or delayed filling of lymphatic channels, is the method of choice for evaluating lymphedema when the diagnosis cannot be made clinically.11,21

MAGNETIC RESONANCE IMAGING

Patients with unilateral lower extremity edema who do not demonstrate a proximal thrombosis on duplex ultrasonography may require additional imaging to diagnose the cause of edema if clinical suspicion for DVT remains high. Magnetic resonance angiography with venography of the lower extremity and pelvis can be used to evaluate for intrinsic or extrinsic pelvic or thigh DVT.22,23 Compression of the left iliac vein by the right iliac artery (May-Thurner syndrome) should be suspected in women between 18 and 30 years of age who present with edema of the left lower extremity.24,25 Magnetic resonance imaging may aid in the diagnosis of musculoskeletal etiologies, such as a gastrocnemius tear or popliteal cyst. T1-weighted magnetic resonance lymphangiography can be used to directly visualize the lymphatic channels when lymphedema is suspected.7,11,26

OTHER STUDIES

Echocardiography to evaluate pulmonary arterial pressures is recommended for patients with obstructive sleep apnea and edema.27,28 In one study of patients with obstructive sleep apnea, 93% of those with edema had elevated right arterial pressures.27 Pulmonary hypertension has long been thought to be the cause of edema associated with obstructive sleep apnea. However, one study found that although a high proportion of patients with edema had obstructive sleep apnea (more than two-thirds), nearly one-third of these patients did not have pulmonary hypertension, which suggests a stronger correlation between edema and obstructive sleep apnea than can be explained by the presence of pulmonary hypertension alone.28

Management of Edema

Management of edema should be guided by the underlying etiology, which commonly includes chronic venous insufficiency, lymphedema, DVT, and medication-induced edema, among others (Table 2).

CHRONIC VENOUS INSUFFICIENCY

In patients with chronic venous insufficiency, diuretic therapy should be avoided unless a comorbid condition requires it (e.g., CHF). Mechanical therapies, including leg elevation and compression stockings with 20 to 30 mm Hg for mild edema and 30 to 40 mm Hg for severe edema complicated by ulceration, are recommended.1,4,5,8,29 Compression therapy is contraindicated in patients with peripheral arterial disease. A study of 120 patients with venous ulcers showed that 6% had mixed arterial-venous ulcers.30 In another study, a higher prevalence of peripheral arterial disease was found in women with symptoms of chronic venous insufficiency vs. those without symptoms.31 Thus, measurement of ankle-brachial index should be considered in patients with risk factors for peripheral arterial disease before prescribing compression therapy.

Mixed evidence exists for the use of pneumatic compression devices in patients with chronic venous insufficiency.29,32 However, these devices should be considered for patients in whom compression stockings are contraindicated. For mild to moderate chronic venous insufficiency, oral horse chestnut seed extract may be an alternative or adjunctive treatment to compression therapy.33,34

Local skin and wound care of venous ulcers is essential in preventing secondary cellulitis and dermatitis. Eczematous (stasis) dermatitis, characterized by dry, inflamed, scaling skin overlying superficial varicose veins, often occurs in patients with chronic venous insufficiency.35 Treatment includes daily hydration with emollients and short courses of topical steroid creams for severely inflamed skin.36

LYMPHEDEMA

The mainstay of lymphedema treatment involves complex decongestive physiotherapy, which is composed of manual lymphatic massage and multilayer bandages. The initial goal is to improve fluid resorption until a maximum therapeutic response is reached. The maintenance phase of treatment includes compression stockings at 30 to 40 mm Hg.11,37,38 Pneumatic compression devices have been shown to augment standard therapies. One randomized controlled trial of women with breast cancer–related lymphedema showed statistically significant improvement in lymphatic function following one hour of pneumatic compression therapy.39 In a study of 155 patients with cancer- and non–cancer-related lymphedema, 95% of patients noted reduction in limb edema after using pneumatic compression devices at home.40 Surgical debulking or bypass procedures are limited to severe refractory cases.7 Diuretics do not have a role in the treatment of lymphedema.

DEEP VENOUS THROMBOSIS

Acute thrombotic events are treated with anticoagulation therapy (unfractionated or low-molecular-weight heparin or warfarin [Coumadin]) to prevent progression of a clot or the development of postthrombotic syndrome.13 Postthrombotic syndrome is characterized by chronic leg swelling, pain, cramping, and skin changes including telangiectasias, which occur in 20% to 50% of patients within five years of a thrombotic event.4143 In addition to anticoagulation, compression stockings should be used after a DVT to prevent postthrombotic syndrome. In a Cochrane review of two randomized controlled trials comparing elastic compression stockings (20 to 30 mm Hg) with placebo in patients with DVT, those who wore compression stockings had a statistically significant reduction in the risk of developing postthrombotic syndrome (odds ratio = 0.39; 95% confidence interval, 0.20 to 0.76) after two years.41 A randomized controlled trial of 209 patients with proximal DVT showed that those who received catheter-directed thrombolysis in addition to conservative therapy with compression stockings and anticoagulation had a lower prevalence of postthrombotic syndrome after 24 months compared with conservative therapy alone, suggesting that thrombolysis may be a treatment option for select patients.44

MEDICATION-INDUCED EDEMA

In patients with suspected medication-induced edema, the offending medication should be discontinued if possible. In patients taking calcium channel blockers to treat hypertension, use of an angiotensin-converting enzyme inhibitor may be more beneficial than angiotensin receptor blocker therapy in reducing calcium channel blocker–induced peripheral edema.45,46

OTHER CAUSES

There is no treatment for lipedema. Weight loss does not affect this condition. Complex regional pain syndrome is treated with physical therapy in combination with medications such as systemic steroids and tricyclic antidepressants.47 Obstructive sleep apnea is treated with positive pressure ventilation.48

Data Sources: A PubMed search was performed for clinical reviews, randomized controlled trials, and meta-analyses. Key search terms were edema, oedema, peripheral edema, lower extremity edema, venous insufficiency, deep vein thrombosis, lymphedema, obstructive sleep apnea, and iliac vein syndrome. Also reviewed were the Cochrane database, National Guideline Clearinghouse, Essential Evidence Plus, UpToDate, and the U.S. Preventive Services Task Force website. Search date: January 2012.

The Authors

KATHRYN P. TRAYES, MD, is an assistant professor in the Department of Family and Community Medicine at Thomas Jefferson University Hospital in Philadelphia, Pa.

JAMES S. STUDDIFORD, MD, is a professor in the Department of Family and Community Medicine at Thomas Jefferson University Hospital.

SARAH PICKLE, MD, is an instructor in the Department of Family Medicine and Community Health at Rutgers Robert Wood Johnson Medical School in New Brunswick, N.J. At the time the article was written, Dr. Pickle was a resident in the Department of Family Medicine and Community Health at the University of Medicine and Dentistry of New Jersey's Robert Wood Johnson Medical School.

AMBER S. TULLY, MD, is an assistant professor in the Department of Family Medicine at the Cleveland Clinic in Cleveland, Ohio.

Address correspondence to Kathryn P. Trayes, MD, Thomas Jefferson University, 1020 Locust St., Ste. 157, Philadelphia, PA 19107 (e-mail: Kathryn.trayes@jefferson.edu). Reprints are not available from the authors.

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