Fluid and electrolyte therapy

Chapter 85 Fluid and electrolyte therapy



The management of patients’ fluid and electrolyte status requires an understanding of body fluid compartments as well as an understanding of water and electrolyte metabolism. These principles will be considered along with the commonly encountered fluid and electrolyte disturbances. Recent evidence for the use of fluid therapy in a number of common clinical scenarios will also be presented.



FLUID COMPARTMENTS (Table 85.1, Figure 85.1)



TOTAL BODY WATER


In humans, water contributes approximately 60% of body weight, with organs varying in water content (Table 85.2). The variation of the percentage of total body weight as water, between individuals, is largely governed by the amount of adipose tissue. The average water content as a percentage of total body weight is 60% for males and 50% for females. Total body water as a percentage of total body weight decreases with age, due to a progressive loss of muscle mass, causing bone and connective tissue to assume a greater percentage of total body weight13 (Table 85.3).


Table 85.1 Body fluid compartments































Fluid compartment Volume (ml/kg) % Total body weight
Plasma volume 45 4.5
Blood volume 75 7.5
Interstitial volume 200 20
Extracellular fluid volume 250 25
Intracellular fluid volume 350 35
Total body fluid volume 600 60


Table 85.2 Water content of various tissues



























Tissue % Water content
Brain 84
Kidney 83
Skeletal muscle 76
Skin 72
Liver 68
Bone 22
Adipose tissue 10

Table 85.3 Water content as a percentage of total body weight























Age (years) Males (%) Females (%)
10–15 60 57
15–40 60 50
40–60 55 47
> 60 50 45

Total body water is commonly divided into two volumes, the extracellular fluid (ECF) volume and the intracellular fluid (ICF) volume.2 Sodium balance regulates the ECF volume, whereas water balance regulates the ICF volume. Sodium excretion is normally regulated by various hormonal and physical ECF volume sensors, whereas water balance is normally regulated by hypothalamic osmolar sensors.4






WATER METABOLISM


Water balance is maintained by altering the intake and excretion of water. Intake is controlled by thirst, whereas excretion is controlled by the renal action of antidiuretic hormone (ADH). In health, plasma osmolalities of about 280 mOsm/kg suppress plasma ADH to concentrations low enough to permit maximum urinary dilution.5 Above this value, an increase in ECF tonicity of about 1–2% or a decrease in total body water of 1–2 l, causes the posterior pituitary to release ADH, which acts upon the distal nephron to increase water reabsorption. Maximum plasma ADH concentrations are reached at an osmolality of 295 mOsm/kg.5 The osmotic stimulation also changes thirst sensation and, in the conscious ambulant individual, initiates water repletion (drinking), which is more important in preventing dehydration than ADH secretion and action. Thus, in health, the upper limit of the body osmolality (and therefore serum sodium) is determined by the osmotic threshold for thirst, whereas the lower limit is determined by the osmotic threshold for ADH release.6


Increase in osmolality caused by permeant solutes (e.g. urea) does not stimulate ADH release. ADH may also be released in response to hypovolaemia and hypotension, via stimulation of low and high pressure baroreceptors. ADH release is extremely marked when more than 30% of the intravascular volume is lost. ADH may also be stimulated by pain and nausea, which are thought to act through the baroreceptor pathways.4 ADH release may also be stimulated by a variety of pharmacological agents (Table 85.4). Renal response to ADH depends upon an intact distal nephron and collecting duct, and a hypertonic medullary interstitium. The capacity to conserve or excrete water also depends upon the osmolar load presented to the distal nephron.4


Table 85.4 Drugs affecting ADH secretion

































Stimulate Inhibit
Nicotine Ethanol
Narcotics Narcotic antagonists
Vincristine Phenytoin
Barbiturates  
Cyclophosphamide  
Chlorpropamide  
Clofibrate  
Carbamazepine  
Amitriptylline  


WATER REQUIREMENTS


Water is needed to eliminate the daily solute load, and to replace daily insensible fluid loss (Table 85.5). With a normal daily excretion of 600 mOsm solute, maximal and minimal secretions of ADH will cause urine osmolality to vary from 1200 to 30 mOsm/kg respectively, and the urine output to vary from 500 ml to 20 l/day respectively. Skin and lung water losses vary, and may range from 500 ml to 8 l/day depending on physical activity, ambient temperature and humidity.





ELECTROLYTES


Chemical compounds in solution may either:






SODIUM


Sodium is the principal cation of the ECF and accounts for 86% of the ECF osmolality. In a 70-kg man, total body sodium content is 4000 mmol (58 mmol/kg) and is divided into a number of compartments (Table 85.7). ECF concentration of sodium varies between 134 and 146 mmol/l. The intracellular sodium concentration varies between different tissues, and ranges from 3 to 20 mmol/l.


Table 85.7 The sodium compartments in a 70-kg man































  Total (mmol) (mmol/kg)
Total body sodium 4000 58
Non-exchangeable bone sodium 1200 17
Exchangeable sodium 2800 40
Intracellular sodium 250 3
Extracellular sodium 2400 35
Exchangeable bone sodium 150 2

The standard Western society dietary sodium intake is about 150 mmol/day, but the daily intake of sodium varies widely, with urinary losses ranging from < 1 to > 240 mmol/day.7 Sodium balance is influenced by renal hormonal and ECF physical characteristics. The complete renal adjustment to an altered sodium load usually requires 3–4 days before balance is restored.



HYPONATRAEMIA


Hyponatraemia is defined as a serum sodium less than 135 mmol/l and may be classified as isotonic, hypertonic or hypotonic, depending upon the measured serum osmolality (Table 85.8).


Table 85.8 Common causes of hyponatraemia













Transurethral resection of prostate (TURP) syndrome



Clinical features

The TURP syndrome consists of hyponatraemia, cardiovascular disturbances (hypertension, hypotension, bradycardia), an altered state of consciousness (agitation, confusion, nausea, vomiting, myoclonic and generalised seizures) and, when using glycine solutions, transient visual disturbances of blurred vision, blindness and fixed dilated pupils, following TURP. It has also been described following endometrial ablation.10 It may occurwithin 15 minutes or be delayed for up to 24 hours postoperatively,11 and is usually caused by an excess absorption of the irrigating fluid which contains 1.5% glycine with an osmolality of 200 mosm/kg. Hyponatraemic syndromes have also been described when irrigating solutions containing 3% mannitol or 3% sorbitol have been used. Symptomatology usually occurs when > 1 l of 1.5% glycine or > 2–3 l of 3% mannitol or sorbitol are absorbed.12


The excess absorption of irrigating fluid causes an increase in total body water (which is often associated with only a small decrease in plasma osmolality), hyponatraemia (as glycine, sorbitol or mannitol reduces the sodium component of ECF osmolality) and an increase in the osmolar gap.12,13 When glycine is used, other features include hyperglycinaemia (up to 20 mmol/l; normal plasma glycine concentrations range from 0.15 to 0.3 mmol/l), hyperserinaemia (as serine is a major metabolite of glycine), hyperammonaemia (following deamination of glycine and serine), metabolic acidosis and hypocalcaemia (due to the glycine metabolites glyoxylic acid and oxalate). Because glycine is an inhibitory neurotransmitter, and as it passes freely into the intracellular compartment when glycine solutions are used, hyperglycinaemia may be more important in the pathophysiology of this disorder than a reduction in body fluid osmolality and cerebral oedema.14




Syndrome of inappropriate ADH secretion (SIADH)


This syndrome is a form of hyponatraemia in which there is an increased concentration of ADH inappropriate to any osmotic or volume stimuli that normally affect ADH secretion.16 Diagnostic criteria and common causes are listed in Tables 85.9 and 85.10, respectively.


Table 85.9 Criteria for the diagnosis of syndrome of inappropriate antidiuretic hormone (SIADH)












Table 85.10 Aetiologies of syndrome of inappropriate antidiuretic hormone (SIADH)






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Jul 7, 2016 | Posted by in CRITICAL CARE | Comments Off on Fluid and electrolyte therapy

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