electrolyte inbalance

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    ELECTROLYTE INBALANCE

    Patria Adri Wibhawa

    Clinical Rotation Student

    Internal Medicine Medical School of

    Christian university of Indonesia, jakarta

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    HYPONATREMIA

    Defined as an abnormally low serum sodium

    concentration (135 mEq/L)

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    Etiology and classification

    I. Pseudohyponatremia

    A. Hyperlipidemia High lipid serum and normalosmolality

    B. Hyperglicemia Finding hyponatremia andhyperglicemia with normal or elevated serumosmolality

    II. Hyponatremia with increased body total sodium

    This is a state in which an excess of total bodysodium and an event greater excess of total bodywater Edema, ascites or both. Serum osmolality islow CHF, Cirrhosis hepatic, SN

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    III. Hyponatremia with decreased total body

    sodium

    Condition associated with both sodium and

    water depletion are characterized by the

    abcense of edema or ascites Symptom and

    sign tachycardia, decreased sentral venous

    pressure, a high hematocrite elevated serumtotal protein may be present

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    A. Decreased Urin sodium concentration (10mEq/L), Ussualy associated with :

    a. Decreased chloride concentration

    1. GI losses- Vomiting or nasogatric suction or both

    - Diarrhea

    2. Exessive respiration with replacement of waterbut not of the sodium losses

    3. Volume depletion without replacemennt of lossfluid and electrolyte after diuretic therapy

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    B. Increaesd urin sodium concentration (10

    mEq/L)

    Causes include adenocortical insufficiency and

    salt losing nephropathy

    4. Hyponatremia with normal Total body sodium

    The disorders include in this category are not

    associated with edema or volume depletionA. Hypothyroidism or glucocorticoid deficiency may be

    associated with euvolemic hyponatremia

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    B. SIADH

    This condition may be idiopathic or may associated

    with one of the following disorder, diseases of the

    central nervous system (Stroke, meningitis),Pulmonary diseases ( TBC, pneumonia), drugs

    (Chlorpropamide, narcotics, barbiturates, vincristine,

    antidepressants and clofibrate).

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    1.Criteria for diagnosis :

    a. Hypotonicity of the body fluids

    b. Urin osmolality greater than 100 mOsm/kg of water

    c. Normal renal, adrenal, and thyroid functiond. Increased urinary excretion of sodium (30mEq/L)

    e. Elevated serum concentration of ADH

    f. Reversal of the syndrome by adequate fluid restriction

    2. CommentWhen a steady state is reached, some of the

    abnormality described may not be present

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    Diagnostic approach

    Once the diagnosis of hyponatremia is made,

    the serum sodium lever should be rhececked

    and the serumm osmolality determined

    1. If the serum osmolality is normal or high in

    the presence of confirm hyponatremia, the

    possibility of hyperlipidemia or hyperglicemia,

    or both should be investigated

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    2. If the serum osmolality is low, confirming the diagnosis oftrue hyponatremia, The satus of the extracelluler fluidvolume should be assesed.

    A. The presence of edema, ascites, rales, and S3 gallop, or

    increaed jugular venous pressure indicate an excess oftotal body sodium.

    B. Postural pulse and BP changes, decreased skin turgor, drymucous membranes or decreased JVP indicate decreased

    total body sodiumC. In the absence of signs of either increased or decreased

    total body sodium TSH and cortisol should be checkedbefore entertaining the diagnose of SIADH

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    Therapeutics

    A. Total Body Water ( Hypovolemia)

    1. If Volume depleted, use NaCL 0,9 % (154 mEq/L)

    2. Calculate sodium deficit :

    - Target sodium = 125-135 mEq/L (130 mEq/L)

    - Sodium deficite = 0,6 x weght in Kg ( desired Na actualNa)

    - Correct at a rate not > 0,5 mEq/L/hours

    Give the patient 50% of calculated amount of sodium inthe first 8 hours and the other 50% in the next 16 hours

    - Use normal saline, do not give hypotonic fluids untilserum sodium is more than 125 mg/L

    3. Correct potassium deficit also

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    Hypokalemia

    Definition

    As an abnormality low serum potassium

    concentration (3,5 mEq/L)

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    Etiology

    I. Non renal causes

    A. Decreased pottasium intake

    B. GI Losses of pottasium

    1. Associated with alcalosis and volume depletiona. Gastric suctioning and vomiting

    b. Chronic laxative abuse ( maybe associated with

    acidosis or normal PH as well)

    2. Associated with acidosis

    a. Diarrheal states ( including villous adenoma or

    Zollinger-Ellison)

    b. Ureterosigmoidostomy

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    II. Renal causes

    A. Pottasium wasting associated with metabolic

    acidosis

    1. Renal tubular acidosis

    2. Postobstructive uropathy

    3. Diuretic phase of acute tubular necrosis4. Chronic pyelonephritis

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    B. Pottasium wasting associated with metabnolic

    akalosis

    1. Diuretic therapy ( Furosemide, ethacrynic acid,

    thiazides)

    2. Disorder with increased aldosteron secretion and

    hipertension ( Primary aldosteronism, renovascular

    hypertension, essensial hypertension with vomitingand diarrhea, diuretic therapy, oral contraception,

    steroid therapy)

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    3. Disorder with increased aldosteron without

    hypertension

    (Salt losing nephropathy, juxtaglomerular

    hyperplasia)

    4. Disorder with normal or decreased aldosteron

    and hypertension ( Cushing syndrom )

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    Symptom and sign

    1. Most symptom are non specific

    anorexia, nausea, vomiting, abdominal

    distension, ileus, weakness, decreased deep

    reflexes, and depressed sensorium.

    2. The ECG finding include lowering, flattening,

    notching, or inversion of the T wave, prominent

    U, depression of the S-T segment and arrhytmia.3. Nephrogenic diabetes insipidus, rhabdomyolysis,

    and aggravation of hepatic coma may also occur

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    Diagnosis approach

    I. Patient with hypokalemia require a through

    investigation to determine whether the pottasium loss

    is the result of renal or extra renal mechanism.

    II. Renal origin 24 hours urinary excretion of

    Pottasium should be measured while the patient is on

    a reguler salt intake

    20 mEq/24 hours especially 60 mEq/24 hoursSuggestive of renal pottasium wasting

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    III. In patient with both metabolic alcalosis and

    pottasium wasting, volume depletion may

    cause the abnormal state to persist.

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    Therapy

    1. Oral ruoteOral pottasium should be given

    preferably asdiluted liquid with or after meals or as

    tablet, which must be swallowed and not allowed

    to

    dissolve in the mouth.

    Oral Kalium 0,75 gm (10mEq) 2-3 days

    Oral KCL solution 15-30 cc

    (1gm KCL = 14 mEq k+)

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    2. Intravenous route

    Max : 10-20 mEq/Hours.

    Higher rate of infusion may be administered ifthe clinical situation warrants a more rapid

    correction of the hypocalemia.

    20-40 mEq in 1 L of saline or dextrose

    solution

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    Hypocalsemia

    Definition

    Hypocalsemia exists when the total serumcalcium value is less than 8,5 mg/100mL.

    Approximately 50% of calcium in blood is boundmainly to albumin and globulins

    The ionized calcium concentration is 5 mg/dL

    and this fraction is biologically active Concurrent measurement of albumin is

    indicated in order to show total serum calcium

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    ETIOLOGY

    The most common cause of hypocalcemia is

    surgically induced hypoparathyroidism.

    Therefore, if a thyroidectomy scar is present,

    the diagnosis is usually obvious.

    A history of antecedent illness, past GI

    surgery, or known underlying renal disease

    may elucidate the cause in other case.

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    I. Hypoparathyroidism

    A. Surgically induced, partial or complete

    Most common

    B. Idopathic

    C. Transient hypoparathyridism of infancy

    (newborn) Usually partial

    D. Bioinactive parathyroid hormon (PTH)

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    II. Reduction in serum albumin

    A. Malabsorption states

    B. Short bowel syndromeC. Chronic liver disease and liver failure

    D. Nephrotic syndrom

    E. Malnutrition III. Pancreatitis

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    IV. Renal disease

    A. Renal tubular dysfunction

    B. Acute tubular necrosisC. Chronic renal failure

    V. Rickets and osteomalasia

    VI. Pseudohyparathyroidism, types I and II

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    VII. Hypoparathyroidism in association withother disease states, which may be familial

    A. Addisons disease

    B. Pernicious anemiaC. Candidiasis

    VIII. Medullary carcinoma of the thyroid,

    sporadic, familial, or in men IX. Hyperphosphatemia

    X. Other vitamin D-related disorders

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    Symptoms

    Usually occur when the total serum calcium

    value is below 7,5 mg/ 100mL, but they

    sometimes occur at higher levels when there

    has been a rapid decrease in the serumcalcium concentration.

    The symptomps are generally those of

    neuromuscular irritability.

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    Symptoms

    I. Numbness and tingling of the face, hand, andfeet

    II. Muscle cramps in the arms, hands, abdomen,legs and feet

    III. Increased number of stools or diarrhea

    IV. Headaches, usually frontal, irritability, anxiety

    V. Difficulty in breathing, particularly noisy

    breathing during exercise or sleepVI. Seizures, which are common, in infants this maybe the only complaint

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    VII. Decreased vision

    VIII. Nail growth abnormalities and infections,delay in cutting teeth

    IX. Dry skin, often infectedX. Weight problem

    A. Weight loss in association with chronicsystemic disease

    B. difficulity in losing weight inpseudohypoparathyroidism

    XI. Bone growth abnormalities or pain (rickets

    and osteomalacia)

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    Sign

    Sign of neuromuscular irritability occur mostoften.

    The following findings may be noted on physical

    examination:1. Thyroidectomy scar

    2. Dry skin

    3. Abormal or infected nails

    4. Cataracts

    5. Chovsteks sign

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    6. Trousseaus sign

    7. Crowing noises during sleep

    8. Seizure disordermay be the finding in infants

    9. Hypotension10. Bone pain or bone abnormalities, including

    abnormal growth, bowing and brachydactylia

    11. Goiter if present may suggest medullarycarcinoma of the thyroid, chronic thyroiditis orgraves disease

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    Diagnostic Approach Hypocalcemia

    Initial Investigation

    The most common

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    THERAPY

    Medication : Is to correct the deficiencys with

    IV calcium ( Ca.Gluconas/ Chloride 10%) or

    peroral (Ca.Gluconas/Carbonate); Can give

    with vit D in a higher dose