Lecture 7 Disturbances in genitourinary function Flashcards

1
Q

Hormonal functions of the kidneys

A
  1. Renin - helps regulate blood pressure.

2. Erythropoietin - stimulates red blood cell production in the bone marrow.

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2
Q

The kidneys convert vitamin D into _

A

Its active form, calcitriol, which is necessary for calcium metabolism.

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3
Q

Approximate bladder capacity (volume) of a child

A

of oz = Child’s age in years + 1

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4
Q

Normal urine specific gravity

A

1.016 - 1.022

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5
Q

Normal urine pH

A

4.8 - 7.8 (average: 6)

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6
Q

Normal blood urea nitrogen (BUN)

A

5 - 18 mg/dL

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7
Q

Urinary tract infection (UTI)

A
  1. The presence of a significant number of microorganisms in the urinary tract, usually caused by ascending bacteria - excludes the distal one-third of the urethra, which is normally colonized by some bacteria.
  2. Most common microorganism: E. coli (approximately 80% of UTIs in children).
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8
Q

Cystitis

A

Infection of the bladder.

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9
Q

Pyelonephritis

A

Infection of the kidney.

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10
Q

UTIs by age and gender

A
  1. Neonates = roughly equal incidence for both genders.
  2. Infants and older = UTIs are 10-30% more frequent in girls.
  3. Age 4 = age of maximum incidence for both genders.
  4. Girls have an approximately 50% greater recurrence rate than boys.
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11
Q

Clinical manifestations of UTIs

A
  1. Infants = fever or hypothermia in neonate; irritability; poor feeding; vomiting; dysuria (painful or burning urination); change in urine odor or color.
  2. Children = abdominal or suprapubic pain; frequency, urgency; dysuria; new or increased incidence of enuresis.
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12
Q

The most important host factor in determining whether a UTI will occur is _

A

Urinary stasis - urine provides an excellent medium for the growth of bacteria, fungi, etc.

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13
Q

Changes in urine odor or color with UTIs

A

Urine will appear cloudy or hazy; strands of pus or mucus; “fishy” odor. Pus visible on micro-exam and at least one bacterium visible on Gram stain (in a single drop of urine).

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14
Q

Clinical manifestations of pyelonephritis

A

May appear similar to a UTI. Most common symptoms include fever, back pain, nausea/vomiting, lethargy, poor appetite, and costovertebral angle tenderness.

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15
Q

Voiding cystourethrography (VCUG)

A

Contrast medium injected into bladder through urethral catheter until bladder is full; films taken before, during, and after voiding.

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16
Q

Intravenous pyelography (IVP)

A
  1. Intravenous injection of a contrast medium; medium secreted and concentrated by tubules; X-ray films obtained beginning 5 minutes after injection.
  2. Usually reserved for situations where there not enough information derived from the other tests.
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17
Q

Checking for evidence of pinworms

A

Pinworms infect the GI tract but may cause vaginitis because they exit at night to lay eggs. At night, apply a strip of tape across the anus; peeling the strip off in the morning will reveal the presence of worms.

18
Q

Antibiotics of choice for UTIs

A

Bactrim or Septra (trimethoprim-sulfamethoxazole); Amoxil (amoxicillin).

19
Q

Recommended daily fluid intake to prevent UTIs

A

About 100 mL/kg/day.

20
Q

Recommended voiding frequency to prevent UTIs

A

At least every 2 hours.

21
Q

Vesicoureteral reflux (VUR)

A
  1. The retrograde flow of bladder urine into the ureters; increases the chance for and perpetuates infections.
  2. Familial pattern: Increased incidence among siblings; increased incidence among children of parents who have had VUR.
  3. Interventions: Low-dose antibiotic therapy (must finish entire course of antibiotics even if asymptomatic) and frequent urine cultures. Surgery used in severe cases.
22
Q

Glomerulonephritis

A
  1. A group of kidney diseases where the glomerulus is injured - capillaries of glomerulus are inflamed.
  2. Occurs from infection, systemic disease process, or as a primary defect in the glomerulus itself.
  3. Manifestations: Periorbital edema - especially in the morning, cola- or tea-colored urine (hematuria), decreased urine output, hypertension, fatigue.
23
Q

Most common form of glomerulonephritis in children

A

Acute post-streptococcal glomerulonephritis (APSGN), an immune-complex disease which can occur 1-3 weeks after strep infection of the throat or skin.

24
Q

Diagnosis of acute post-streptococcal glomerulonephritis (APSGN)

A
  1. Urinalysis - hematuria, proteinuria, urine specific gravity increased to 1.020.
  2. ASO titer level will be increased - indicates a recent strep infection.
  3. C3 (serum complement level) will be decreased initially but returns to normal 8-10 weeks after onset of glomerulonephritis.
  4. VCUG, renal scan for evidence of scarring, urodynamic studies for voiding dysfunction.
25
Q

The most effective measure for fluid balance in children is _

A

Monitoring their daily weight (same time, same scale, same amount of clothing).

26
Q

Implementing fluid restrictions in children

A

Review output (e.g., for the previous 8 hours). For the next 8 hours, the child will only be allowed to have that amount of fluid, plus a small amount for insensible water loss.

27
Q

Treatment of acute post-streptococcal glomerulonephritis (APSGN)

A

No specific treatment; antibiotics will only be used if there is evidence of a persistent strep infection. Antihypertensives and diuretics may be used (diuretics will not be used in cases of severe renal failure).

28
Q

Normal serum creatinine

A

0.3 - 0.7 mg/dL.

29
Q

Nephrotic syndrome

A
  1. The most common presentation of glomerular injury in children.
  2. Characterized by massive proteinuria, hypoalbuminemia, hyperlipidemia, and edema.
30
Q

Important nursing intervention for children with nephrotic syndrome

A

Provision of good skin care and frequent turning - these children are prone to skin breakdown.

31
Q

Minimal-change nephrotic syndrome (MCNS)

A
  1. Most common type of nephrotic syndrome in children (about 80%; predominately occurs in school-aged children).
  2. Cause is obscure, but is often preceded by a viral upper respiratory infection.
32
Q

Secondary nephrotic syndrome

A
  1. Occurs after or in association with glomerular damage of known etiology.
  2. Main presenting symptom of renal disease in pediatric AIDS.
33
Q

Congenital nephrotic syndrome

A
  1. Recessive genetic disorder; children are born small for gestational age, with proteinuria and edema present at birth.
  2. Fatal by 2 years of age unless the child undergoes dialysis or renal transplantation.
34
Q

Renal tubular disorders

A
  1. One or more abnormalities in specific mechanisms of tubular transport or reabsorption.
  2. May be minimally disruptive to renal function or result in major renal failure.
  3. Metabolic disturbances are the primary manifestations: Failure to thrive, metabolic bone disease, persistent acidosis. Usually these children present with no edema, no blood pressure abnormalities, and their BUN and UA are WNL.
35
Q

Proximal tubular acidosis (Type II)

A
  1. Caused by impaired bicarbonate reabsorption in the proximal tubule.
  2. Fanconi syndrome - complex form which can be acquired or hereditary, with growth failure and tachypnea as the major symptoms.
36
Q

Distal tubular acidosis (Type I)

A
  1. Caused by the inability of the kidney to establish a normal pH gradient between tubular cells and tubular contents.
  2. Most characteristic feature is the inability to produce a urinary pH below 6.0 despite the presence of severe metabolic acidosis.
  3. Therapy involves administration of bicarbonate or citrate to correct imbalances and electrolyte disorders.
37
Q

Nephrogenic diabetes insipidus

A
  1. Characterized by renal tubular resistance to the antidiuretic hormone arginine vasopressin (AVP) - leads to an inability to concentrate urine, with subsequent polyuria and compensatory polydipsia.
  2. May be hereditary (X-linked recessive) or acquired.
38
Q

Hemolytic uremic syndrome

A
  1. Acute renal disease characterized by the triad of nephropathy, thrombocytopenia and microangiopathic hemolytic anemia.
  2. Usually follows an acute GI or upper respiratory infection.
  3. A leading cause of acute renal failure in early childhood; primarily occurs between the ages of 6 months and 3 years.
39
Q

Chronic renal failure (CRF) in children

A

Most common complaint: growth impairment. Child presents with short stature, especially in combination with polyuria, frequent bouts of dehydration, salt craving, bone deformities, abnormal tooth development, lethargy, anemia, history of upper respiratory infections or glomerulonephritis.

40
Q

Interventions for chronic renal failure (CRF)

A
  1. Nutrition: Provide 100% of RDA for calories; low sodium diet and fluid restriction; vitamin D and water-soluble vitamin supplementation; possible phosphorus restriction.
  2. Medications: Phosphorus binders (i.e., calcium carbonate) - correction of osteodystrophy; alkalizing agents (i.e., sodium bicarbonate) - correction of acidosis; recombinant human erythropoietin and/or iron supplements often needed to correct anemia.
  3. Antihypertensives: Diuretics, beta-blockers and vasodilators may all be used.