Towards an understanding of edema
Charles J Diskin, clinical associate professor, Thomas J Stokes, clinical associate professor, Linda M Dansby, clinical associate professor, Thomas B Carter, clinical associate professor, Lautrec Radcliff, clinical associate professor, and Selby G Thomas, associate professor
Hypertension, Nephrology, Dialysis, and Transplantation Clinic, School of Pharmacy, Auburn University, Auburn, AL 36849, USA
Correspondence to: Dr Diskin HNDT512@auburn.campuscw.netSometime during the reign of Tiberius (25-50 ad) Celsus wrote:
A chronic malady may develop in patients who collect water under their skin. The Greeks call this hydrops.
There are three species:
(1)Sometimes the belly is tense. The Greeks call this tympanites.
(2)Sometimes the body is rendered uneven by swellings arising here and there and all over. The Greeks call this hyposarka.
(3)Sometimes, the water is all drawn within and is called ascites.1
Oedema has been recognised almost since the earliest recordings of medical history. Even the ancient Egyptians seem to have had a hieroglyphic for “water under the skin.” In the description of case number four in the Edwin Smith papyrus the hieroglyphic appears to be similar to the one used for water that floods from the Nile.2 This ancient familiarity, however, has not yet led to a complete understanding of oedema, and sometimes its treatment remains imperfect. None the less, an improved understanding of the pathophysiology and biophysics of oedema will allow most doctors to develop a more rational approach to treating it.
The causes of oedema are not well understood
Three main variables are associated with the formation of oedema: oncotic (colloid osmotic) pressure, hydrostatic pressure, and membrane permeability
Differential diagnosis should be based on an understanding of which of the variables has been altered
Osmotic pressure is a measure of the entropy of the solution
Entropy can be altered without changing the number of molecules in a protein solution if the arrangement of those molecules is changed
This article is based mostly on our own research and clinical experience.
When Bright first described the retention of water and waste by diseased kidneys3 he was deliberately vague about whether he was describing one disease or two since he could not explain water retention without uraemia, nor could he explain uraemia without oedema.4 After more than half a century, Starling defined the physiological forces involved in the production of oedema.5 Those forces included the difference between intracapillary blood pressure and extravascular hydrostatic pressure (P), differences in oncotic (colloid osmotic) pressure (π), and the permeability of the blood vessel wall (Kf). These remain the primary variables used to characterise fluid movement (FM) and the formation of oedema:
Although up to 4.5kg of excess total body fluid may be present without physical evidence of oedema, inspection and palpation are usually sufficient to identify it. Compression of the skin with a finger often results in “pitting”; this can be a useful aid in judging the amount of oedema and the type. After 10 seconds’ compression of the affected skin, the resulting depth in millimetres can be used to determine the amount of oedema, which is classed as ranging from trace to +4; the amount of oedema is classed as +4 in cases in which an indentation or “pit” of a depth greater than or equal to the depth of one’s fingers occurs. If the length of time that the pit remains in the skin after the finger is withdrawn is less than 15 seconds then low oncotic pressure is the likely cause of the oedema; if it is greater than 15 seconds a high capillary hydrostatic pressure should be suspected. Localised oedema is most likely to result from a local alteration. Generalised oedema is often most prominent in the lower extremities in ambulatory patients and in the presacral region in those who are confined to bed. Gravitational effects alone usually explain such distributions; however, children with kidney disease sometimes exhibit periorbital oedema (fig 1).
The table presents the clinical classification of the causes of oedema using a rational approach which is based on identification of the underlying physiological alteration. A typical algorithm for the diagnosis and treatment of oedema is shown in figure 2.
Increased permeability of the blood vessel wall
Changes in the permeability of the capillary wall are common. When Celsus described the classic signs of inflammation (redness, heat, swelling, and pain), he was describing an increase in permeability.1 Today we know that cytokines, such as tumour necrosis factor, interleukin 1, and interleukin 10 (fig 3) mediate increases in vascular permeability.
In addition to the localised oedema of inflammation, childhood nephrotic syndrome caused by minimal change disease results from an altered permeability of the glomerular capillary bed and the ensuing proteinuria. The loss of plasma proteins causes a decrease in oncotic (colloid osmotic) pressure which promotes further fluid movement. Similarly, although the difference between intracapillary blood pressure and extravascular hydrostatic pressure, and the difference in oncotic pressure probably play a greater part in the development of oedema in patients with cirrhosis, an increase in circulating vasodilatory prostaglandins, nitric oxide, and various gut hormones also alters vascular permeability.
Increased difference between intracapillary and extravascular pressure
Raised capillary venous pressure occurs in cases of salt and water retention; renal failure with oliguria may be one cause. The most discriminating diagnostic finding is the presence of increased circulating concentrations of urea and creatinine. Ultrasound examination of the kidneys may be useful in distinguishing acute, and often reversible, renal failure from chronic, and irreversible, renal insufficiency.
Venous and lymphatic obstruction may cause localised oedema. Deep venous thrombosis often presents with a palpable vein or occasionally a positive Homans’s sign but without oedema caused by collateral drainage. Phlegmasia cerulea dolens (blue phlebitis) occurs when the major deep veins are occluded with a thrombus and thus results in a marked increase in hydrostatic pressure within the venous system.
Left sided heart failure usually leads to pulmonary oedema as a result of increased pulmonary capillary wedge pressures. Once the right side of the heart begins to fail, increased pressures result in peripheral oedema (fig 4).
Raised portal venous pressure can cause ascites. This type of increase is primarily the result of scarring of the hepatic parenchyma which increases the vascular resistance in postsinusoidal venules; there are also increased circulating concentrations of renin, angiotensin, and aldosterone that are thought to be the result of a decrease in the effective circulating blood volume. However, the nebulous concept of a “decreased effective circulating blood volume” is often little more than a consequence of reduced oncotic pressure (fig 4). When the elevated portal pressure has been caused by cirrhosis of the liver, lower oncotic pressure may occur as a result of the loss of the ability of the liver to synthesise plasma proteins, a process which acts through the renin-angiotensin-aldosterone axis to further increase the difference between intracapillary blood pressure and extravascular hydrostatic pressure.
Decreased oncotic (colloid osmotic) pressure
The nephrotic syndrome, liver disease, and kwashiorkor are the most common examples of disorders that cause oedema when there is a loss of oncotic pressure. The nephrotic syndrome encompasses a constellation of signs and symptoms (proteinuria >3.5g per 24 hours, hypoalbuminaemia, lipiduria, hypercholesterolaemia, and oedema), but many clinicians often incorrectly use “nephrotic range proteinuria” as a synonym for the nephrotic syndrome. Nevertheless, proteinuria remains the most salient finding in establishing the diagnosis.
Although a decreased serum concentration of albumin may indicate excessive renal loss and paired white lines in the fingernails are often present on examination, it may also have been caused by a reduction in the capability of the liver to synthesise plasma proteins. In such cases a prolonged prothrombin time combined with other evidence of liver disease may lead to a confirmatory diagnosis of cirrhosis by biopsy (table).
A number of formulas have been derived to predict oncotic pressure from serum protein concentrations. However, we have not been able to adequately predict which patients would develop oedema using a given concentration of serum proteins.6 Moreover, there have been reports of patients with AIDS nephropathy who have not developed oedema, despite severely decreased concentrations of plasma proteins.7 One study showed that protein from patients with kidney disease did not behave similarly to protein from normal controls; it often exerted a much lower oncotic pressure when measured in vitro by a synthetic membrane in a colloid osmometer.8 Furthermore, when the plasma proteins were concentrated or diluted, plasma from patients with kidney disease showed a great variation in the predictability of oncotic pressure.8 To understand oedema, doctors must understand oncotic (colloid osmotic) pressure (box).
Treatment should always focus on correcting the underlying cause of the oedema. Our approach has been to determine which variable (permeability of the blood vessel wall, difference between intracapillary and extravascular pressure, or difference in oncotic pressure) has become deranged and then to treat the disease that has altered that variable. For localised oedema caused by infection, hypothyroidism, or an autoimmune reaction, treatment should be with antibiotics, thyroid replacement, and steroids respectively.
If the oedema is the result of decreased cardiac function then inotropic agents such as digoxin or dobutamine may be useful in conjunction with afterload reduction with angiotensin converting enzyme inhibitors or angiotensin receptor blockers.
If the nephrotic syndrome is identified by renal biopsy as an autoimmune phenomenon, immunosuppression may prove useful. Similarly, if the renal pathology seems to be caused by glomerulosclerosis or hyperfiltration, angiotensin converting enzyme inhibitors may be beneficial. In cases of oliguric renal failure, dialysis may be required for volume removal.
In kwashiorkor and oedema caused by nutritional deficiency, improved nutrition may initially result in “refeeding oedema” because of the effect of increased insulin concentrations on sodium retention.
Restriction of salt and water intake has been used to treat generalised oedema since the days of Celsus for cases in which the underlying cause cannot be treated. In such cases diuretics are usually used; however, they should not be used for reasons that are merely cosmetic. Because they stimulate the production of aldosterone, diuretics have been implicated in the aggravation of the cyclical oedema of women (a disorder of periodic oedema associated with menstruation and often called idiopathic or diuretic induced oedema). Similarly, the complications of loop diuretics may make their use counterproductive. In fact, the metabolic alkalosis that arises from the inhibition of chloride reabsorption may actually result in a worsening of the oedema because of a decrease in oncotic pressure. This may be a contributing factor in the production of the idiopathic oedema associated with the use of diuretics.
Albumin infusions create an ephemeral improvement and are of little value11; they carry the risks associated with the infusion of any blood product. Ascites reinfusion, in which ascitic fluid is transferred back into the vascular space either by removal and subsequent reinfusion through a peripheral vein or by continuous reinfusion with a peritoneal-atrial, or Leveen, shunt can be useful in treating cirrhosis, particularly when a peritoneal-atrial or peritoneal-venous shunt is surgically created. “Head out immersion” treatment can increase extravascular hydrostatic pressure thereby decreasing the difference between intracapillary pressure and extravascular hydrostatic pressure, but the effect will last only as long as the body is immersed under water, so it is not a practical solution. Support stockings and limb elevation provide the same effect. Captopril may be useful in treating the cyclical oedema of women because it inhibits production of aldosterone and bradykinin.12
Can alterations be made to plasma to restore free entropy and avoid the need for diuretics or albumin infusions? Theoretically, the answer is “yes.” The addition of a solitary carbon atom to the tail of a variable alkyl chain, a colloid, has been shown to alter its osmotic coefficient.13 Antioxidants might help, since oxidation stress results in greater surface hydrophobicity. Work is just beginning into many of the theoretical areas of intervention.
Some day we may be able to treat oedema caused by the nephrotic syndrome by restoring free entropy to the plasma rather than by using diuretics. Perhaps we might be able to maintain oncotic pressure even in the presence of decreased concentrations of plasma proteins, in a manner similar to the Nargase analbuminaemic rats, a strain of rat that cannot synthesise albumin.14 Then, for the first time since Celsus, we would actually be addressing the problem rather than merely the symptom of water retention
Competing interests: None declared.
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