34. generalised Edema Flashcards

1
Q

causes of bilateral edema- systemic ones

A
Systemic:
PREGNANCY
Congestive cardiac failure.
Hypoproteinaemia, eg liver failure, nephrotic syndrome, malnutrition, protein-losing enteropathy.
Renal failure.
Fluid overload.
Anaemia.
Drugs, eg calcium antagonists, non-steroidal anti-inflammatory drugs.
Hypothyroidism.
Hereditary angioneurotic oedema.
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2
Q

causes of acute local unilateral edema?

A
Local:
Acute:
Trauma
Deep vein thrombosis
Cellulitis
Allergic reaction
Rheumatoid arthritis
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3
Q

causes of chronic local unilateral edema?

A

Chronic:
Venous: varicose veins, obstruction of venous return, eg pregnancy, pelvic tumours, inferior vena cava obstruction, post-phlebitis.
Lymphoedema: lymphatic obstruction due to malignancy, post-irradiation, surgery, recurrent infection, lymphatic hypoplasia, filariasis.
Congenital malformations, eg arteriovenous fistula.
Stasis: paralysis, poor mobility and dependency, obesity.

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4
Q

name some investigations to be carried out in (bilateral leg) edema?

A

Urinalysis: proteinuria suggests renal cause.

FBC: high white cell count in infection; anaemia.

Biochemistry: renal function and electrolytes (raised creatinine in renal failure); LFTs (impaired liver function and associated low albumin); glucose (infection associated with diabetes); TFTs (hypothyroidism).
CRP
Clotting screen: abnormal clotting associated with spontaneous haematoma.
CXR: pulmonary oedema.
D-dimer blood test: D-dimers are products of fibrin degradation and are raised in patients with venous thromboembolism. Sensitivity of the test is high but specificity is poor.
ECG: heart failure.
Ultrasound, CT scan: haematoma, tumour, abdominal or pelvic mass.
Duplex Doppler, venography: deep vein thrombosis, arteriovenous fistula.
Lymphangiography: demonstrates cause of lymphoedema and whether due to hypoplasia or obstruction.
Lymph node biopsy: infection, tumour.
Other investigations may include renal biopsy, echocardiogram.

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5
Q

name an infection causing nephrotic syndrome?

A

Glomerulonephritis can present with different clinical syndromes. These include nephrotic and nephritic syndrome (post streptococcal infections)

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6
Q

what are the 4 main clinical features of nephrotic syndrome?

A
  • –Proteinuria (formerly defined as >3.5 g/day but there appears to be individual variation around this cut-off figure).
  • –Hypoalbuminaemia as a result of urinary protein loss (albumin levels usually in range
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7
Q

Primary renal causes of nephrotic syndrome?

A
  • —–Minimal-change glomerular disease (15%) - the most common cause in children.
  • –Focal segmental glomerulosclerosis (35% of nephrotic syndrome) - the most common cause of idiopathic nephrotic syndrome in adults.
  • —-Membranous glomerular disease (33%).
  • ——Membranoproliferative glomerulonephritis (14%).
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8
Q

name secondary renal disease causing nephrotic syndrome?

infections?drugs?metabolic?inherited?malignant? pregnancy?

A

—-Post-infectious causes - eg, Group A beta-haemolytic streptococci, tuberculosis, malaria, syphilis, viruses (such as varicella-zoster, hepatitis B, human immunodeficiency), infectious mononucleosis.

Metabolic diseases - eg, diabetes mellitus, amyloidosis.

Inherited disease - eg, Alport’s syndrome, hereditary nephritis, sickle cell disease.

Malignant disease - eg, multiple myeloma, leukaemia, lymphoma, carcinoma of breast/lung/colon/stomach.

Medications - eg, non-steroidal anti-inflammatory drugs (NSAIDs), captopril, lithium, gold, diamorphine, interferon-alpha, penicillamine, probenecid and many others.

Toxins - eg, bee sting, snake bites, phytotoxins.

Pregnancy - eg, pre-eclampsia.
Transplant rejection.

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