Electrolyte + Acid base Disorders Flashcards

1
Q

Causes of Hypernatremia

A

(1. ) Water loss
- Dehydration
- Diuretics
- DI
- Osmotic diuresis e.g. HHS
- Diarrhoea/ Vomiting/ Sweating/ Burns

(2. ) Excessive hypertonic fluid
- IV infusion
- Total parental nutrition
- Enteral feeds (NGT)

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2
Q

Signs + syx of Hypernatremia

A
  • Lethargy
  • Weakness
  • Confusion
  • Agitation
  • Seizure
  • DI: polydipsia, polyuria, thirst
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3
Q

Ix and Mx of Hypernatremia

A

Ix: UE, Ca, Glucose

Mx: PO or IV fluids

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4
Q

Cause of HYPOnatremia

A

Caused by water excess or sodium depletion

(1. ) Hypovolaemic hyponatremia
- Diuretic therapy
- Addison’s: inadequate steroids and thus Na resorption
- Burns/diarrhoea/ vomiting - body loses electrolytes + water

(2. ) Euvolemic
- Hypothyroidism

(3. ) Hypervolemic hyponatremia
- SIADH: too much ADH release, too much water reabsorbed so serum Na drops
- HF, kidney, liver disease, causes fluid to accumulate in body which dilutes Na in body
- Hypalbuminaemia
- Nephrotic syndrome

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5
Q

Presentation of HYPOnatremia

A
  • Asyx (particularly if developed slowly or mild)
  • Lethargy
  • Headache
  • Dizziness
  • Postural hypotension
  • Ataxia
  • Severe changes: confusion/psychosis/seizures
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6
Q

Hx/Ex/Ix of HYPOnatremia

A

Hx:

  • Any recent illness e.g. gastroenteritis
  • PMH: any chronic illnesses such as anorexia nervosa, HF, CKD
  • DH: thiazides, steroids?

Ex

  • Determine volume status
  • Assess HR, postural change in BP, JVP, oedema, signs of dehydration - dry skin/mucous mb/low uo/reduce skin tugor
  • Ask about fluid intake and inspect them
  • Are they dehydrated/euvolemic/oedematous ?

Ix

(1. ) Serum Na and osmolarity
(2. ) Urine Na or osmolarity
(3. ) Further ix if necessary:
- Urinalysis - if renal disease
- TFT
- Serum cortisol, ACTH - if AI
- BNP - if HF
- LFT

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7
Q

Mx of HYPOnatremia

A

Admit if:

  • Acute onset or severe Na (<125)
  • Syx: CNS disturbance, confusion, headache, drowsiness, coma/altered GCS, seizures
  • Signs of hypovolaemia

Mx

(1. ) Rx underlying cause e.g. medication, AI, dehydration
(2. ) Hypertonic 1.8% saline (slow inc as rapid inc can lead to Central pontine Myelinolysis)

If not severe, assess fluid status and Rx accordingly

(1. ) Correct underlying cause
(2. ) Hypovolaemia: 0.9% saline cautious rehydration
(3. ) Hypervolaemia: fluid restriction
(4. ) SIADH: Tolvaptan

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8
Q

What is SIADH? Causes? Mx?

A

Inappropriate ADH secretion from pituitary or ectopic source, despite low serum osmolality.

Causes:

  • Small cell lung ca – tumour produced ADH
  • Atypical pneumonia (legionella)
  • Brain damage: meningitis, SAH, Head injury, tumour,
  • Medications: Carbamzepine, ssri

Management

  • Restrict fluid intake
  • Rx underlying cause
  • Tolvaptan (competitive ADH-R antagonist, so prevent ADH binding)
  • If severe hyponatremia: Hypertonic IV fluid
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9
Q

Hyperkalaemia: causes, presentation

A

Causes:

  • Kidney: AKI, CKD
  • Rhabdomyolysis
  • Addison’s
  • Medication: aldosterone antagonists, ACEi, NSAIDs, K+ supps

Presentation

  • Asyx
  • Weakness
  • Tingling
  • Nauseous
  • Severe/sudden hyperkalaemia: palpitations, SoB, CP, N+V
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10
Q

Hyperkalaemia: Ix, Mx

A

Investigations

(1. ) VBG
(2. ) UE
(3. ) ECG
- Tall, peaked T waves
- Flat or absent P waves
- Broad QRS
- VF

Management
>6.5mmol +/- ECG changes - urgent Rx
(1.) IV Calcium gluconate
(2.) IV insulin + glucose/dextrose
(3.) Nebulised SABA 
(4.) UE + ECG monitoring 
(5.) Check any precipitating factors + lower total body K via:
- Ca resonium = prevent K gut absorption so excreted into stools
- Loop diuretics
- Dialysis 

Non-urgent/ <6mmol K

(1. ) Change in diet
(2. ) Review medication e.g. stop spironolactone or acei

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11
Q

Hypokalaemia: causes, presentation

A

Causes

  • Renal: diuretics, Cushing, hyperaldosteronism, hypomagnesium
  • extra-renal: inadequate oral intake, D+V, alkalosis, burns, excessive sweating

Presentation

  • Asyx
  • Severe: Weakness, paraesthesia, hypotonia, hyporeflexia, tetany
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12
Q

Hypokalaemia: Ix + mx

A

Ix

(1. ) ECG
(2. ) Blood: UE, Cl, HCO3, glucose, mg, ca
(3. ) VBG

Mx
Mild (>2.5, no ECG change, pt can tolerate oral)
(1.) Oral supps (SandoK)
(2.) Rx cause
(3.) Check UE/K+ 3d after

Severe (<2.5)

(1. ) Cardiac, electrolyte, mg monitoring
(2. ) IV 0.9% saline
(3. ) IV K+ 20mmol/h
(4. ) Rx cause

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13
Q

Hypomagnesium causes + presentation + ix + mx

A

Causes

  • Drugs: PPI, diuretics
  • Alcoholism
  • Refeeding syndrome
  • Parental nutrition
  • Severe burns
  • Dec gut absorption: D+V, malabsoprtion (crohns, coeliac), SMALL BOWEL RESECTION***
  • Acute pancreatitis

Presentation

  • asyx
  • hypocalcemia syx: Tetany, Trousseau and Chvostek signs, paraesthesia
  • seizure
  • arrythmia

Ix

(1. ) ECG
(2. ) Serum Mg, Ca, K, PO, glucose
(3. ) 24-hour Mg excretion

Mx

(1. ) Identify and Rx cause e.g. medication
(2. ) IV Mg replacement if <0.4 /tetany/ arrhythmias /seizures
(3. ) PO Mg salts if >0.4

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14
Q

Resp acidosis - what would you seen in ABG, causes?

A

Resp acidosis: Lo pH, hi CO2

Causes

  • Asthma, COPD - Raised HCO3 indicates pt has been retaining CO2 chronically usually seen in COPD.
  • Respiratory depression e.g. opiates, benzodiazapams
  • Guillain-Barre syndrome – inability to ventilate due to paralysis
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15
Q

Resp alkalosis- what would you seen in ABG, causes?

A

Resp alkalosis: Hi pH, lo CO2

Anything causes hyperventilation + RR is high as they are blowing off CO2.

Causes:

  • Anxiety
  • PE - to differentiate between the two PE would also have a lo O2.
  • Salicylate poisoning
  • Altitude
  • Pregnancy
  • Pyrexia
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16
Q

Metabolic acidosis - what would you seen in ABG, causes?

A

Metabolic acidosis: Lo pH, low HCO3

Causes:

  • Raised lactic acid: anaerobic respiration / shock/ infection/ tissue ischaemia
  • Raised ketones: DKA/ alcohol
  • Inc H+: renal failure
  • Reduced HCO3: diarrhoea (stools contain HCO3), renal failure
17
Q

Metabolic alkalosis- what would you seen in ABG, causes?

A

Metabolic alkalosis: Hi pH, hi HCO3

Causes (Loss of H+):

  • vomit (H+ lost)
  • loop, thiazide diuretics
  • Primary hyperaldosteronism
  • Hypokalaemia
  • Burns
  • Bartter’s syndrome