Peds 39 Study Notes on Pediatric Genitourinary Disorders
Chapter 39: The Child With a Genitourinary Disorder
Growth and Development of Genitourinary System #1
Anatomy:
Comprised of the following components:
Kidneys
Ureters
Urinary Bladder
Urethra
Functions:
Excretes excess water and waste products
Maintains balance of electrolytes and acid-base
Regulates blood pressure by producing the enzyme renin
Produces erythropoietin, a hormone that stimulates the production of red blood cells (RBCs).
Growth and Development of Genitourinary System #2
Infants and Children:
Emptying the bladder of urine is a reflex action.
Between ages 2 and 3, children learn to hold urine and urinate voluntarily.
Bladder capacity increases with age.
Female urethra is shorter than male urethra, resulting in a higher risk for urinary tract infections (UTIs).
Kidneys are located lower in the abdomen compared to adults and have less fat cushion which increases the risk of trauma to the kidneys.
Growth and Development of Genitourinary System #3
Urine Output:
Average urine output varies by age, fluid intake, and kidney health.
Growth and Development of Genitourinary System #4
Kidney Development:
Kidneys reach full size and function by adolescence.
The reproductive system matures at puberty, leading to the production of necessary reproductive cells:
Males: Testes, scrotum, ducts, glands, penis.
Females: Ovaries, fallopian tubes, uterus, vagina, external genitalia.
Hormonal changes during puberty enable full development of the reproductive system.
Urinary Tract Infections (UTIs) #1
Prevalence:
Common in the “diaper age”
More frequent in females than males, except during the first 4 months of life.
Etiology:
Caused by various bacteria, with Escherichia coli from the intestinal tract being the most common.
Female urethra is shorter and straighter making it more susceptible to contamination with feces.
Inflammation may extend into the bladder, ureters, and kidneys.
Urinary Tract Infections (UTIs) #2
Clinical Manifestations:
Symptoms include:
Fever
Irritability
Vomiting
Foul-smelling urine
Poor feeding
Weight loss
Abdominal pain
Urgency and increased frequency of urination.
There may be little to no fever present.
If toilet-trained, may experience incontinence or bedwetting.
Acute pyelonephritis: Abrupt onset with high fever lasting 1 or 2 days.
Urinary Tract Infections (UTIs) #3
Diagnosis:
“Clean catch” urine specimen for microscopic examination and possibly culture; for some cases, a sterile specimen may be required.
Treatment:
Simple UTI managed with anti-infective agents for 7 to 14 days.
Acute pyelonephritis may require hospitalization and intravenous (IV) antibiotics; fluids encouraged.
Importance of completing the full course of antibiotics.
Renal and bladder ultrasound conducted to check for possible structural defects in cases of recurrent infections.
Question #1
Is the following statement true or false?
UTIs are more commonly seen in adolescent males than in females.
Answer to Question #1
False
UTIs are more commonly seen in adolescent females than in males.
The female urethra is shorter and straighter, allowing for easier contamination with feces leading to infections by E. coli, which is found in the colon.
Males are more commonly infected during the first four months of life, particularly if not circumcised.
Enuresis #1
Definition:
Continued incontinence of urine beyond the age when control of urination is commonly acquired.
Diurnal enuresis: loss of daytime control.
Nocturnal enuresis: loss of nighttime control, commonly referred to as bedwetting.
It is normal for many children to not acquire complete nighttime control until the ages of 5 to 7 years; occasional bedwetting may be present until ages 9 or 10, particularly more in boys.
Enuresis may persist into adulthood.
Enuresis #2
Causes:
Can be physiologic or psychological in nature:
Physiologic Causes: Physical disorders such as diabetes mellitus, sickle cell anemia; small bladder capacity; urinary tract infection (UTI); constipation; lack of awareness/signals to empty bladder due to deep sleep.
Psychological Causes: Experiences such as rigorous toilet training before the child was ready, expressing resentment towards family, desire to regress to an earlier developmental stage, and emotional stress.
May be a possible sign of sexual abuse.
Enuresis #3
Clinical Approach:
If a physiologic cause is ruled out, efforts should focus on discovering psychological causes.
Family Support: Suggestions for families to help the child achieve control include:
Waking the child during the night to go to the toilet.
Limiting fluid intake before bedtime.
Use of an enuresis alarm.
Healthcare professionals should maintain a supportive and understanding attitude towards the concerns of the family and the child.
Acute Poststreptococcal Glomerulonephritis #1
Condition Overview:
An inflammatory reaction to a specific bacterium known as group A beta-hemolytic streptococcus.
An antigen-antibody reaction occurs causing injury to and blockage of the glomeruli, which permits RBCs and proteins to escape into the urine.
Peak incidence occurs between ages 5 to 12 years, twice as often in boys compared to girls.
The condition resembles nephrotic syndrome.
Prognosis is generally excellent, though it can progress to chronic nephritis.
Acute Poststreptococcal Glomerulonephritis #2
Clinical Manifestations:
Presenting symptoms usually appear 1 to 3 weeks after the onset of streptococcal infection:
Grossly bloody urine, which may appear smoky, tea or cola colored; possibility of edema.
Hypertension occurs in 50% to 90% of affected individuals.
Fever range from 103°F to 104°F (39.4°C to 40°C) at onset, reducing to approximately 100°F (37.8°C).
Other symptoms may include slight headache, lethargy, vomiting, oliguria, hematuria, and proteinuria on urinalysis; elevated BUN, serum creatinine level, or ESR.
Severe headache, drowsiness, seizures, and vomiting may accompany hypertension.
Acute Poststreptococcal Glomerulonephritis #3
Treatment Guidelines:
Limit activities until clinical symptoms subside.
Antibiotics may be prescribed; antihypertensives or diuretics may be utilized as needed.
Dietary restrictions are generally minimal, though extra salt intake may be limited.
Symptoms and complications are treated symptomatically.
Nursing Care:
Bed rest and contact precautions are critical.
Monitor the child’s activity level to prevent fatigue.
Track intake and output; implement restrictions when output is low.
Measure blood pressure and perform urine dipstick tests for protein and blood.
If the condition persists for longer than a year, it may indicate a chronic condition.
Nephrotic Syndrome #1
Overview:
Nephrotic syndrome is not a single condition but encompasses various types of nephrosis.
Idiopathic nephrotic syndrome (minimal change nephrotic syndrome [MCNS]) is the most common in children.
Early characteristics include edema and proteinuria; the onset of MCNS is insidious with a course of remissions and exacerbations, but the recovery rate is generally good with the cause remaining unknown.
Predominantly seen in children under 6 years of age.
Nephrotic Syndrome #2
Clinical Manifestations:
The initial symptom typically is edema, which starts around the eyes and face in the morning and later shifts to the abdomen, lower extremities, and ankles.
Anasarca (generalized edema) may develop, sometimes causing respiratory difficulties with edema shifting positions.
Other symptoms may include loss of appetite, fatigue, irritability, and malnutrition.
Children affected by nephrotic syndrome are susceptible to infections, with repeat acute respiratory conditions commonly occurring.
Nephrotic Syndrome #3
Diagnosis:
Laboratory findings show marked proteinuria in urine samples; hematuria is usually absent.
Blood tests will typically reveal hyperlipidemia and low levels of serum protein and albumin.
Treatment:
The management involves a prolonged period of remissions and recurrences, including corticosteroid therapy, daily urine testing, and potentially immunosuppressant therapy.
Dietary strategies should be appealing to the child; low salt/high protein content is encouraged, along with support and encouragement from family.
Changes in treatment may be necessary if the initial regime is ineffective or complications occur.
Comparison #1: Nephrotic Syndrome vs. Poststreptococcal Glomerulonephritis
Assessment Factors:
Cause:
Nephrotic Syndrome: Idiopathic; possibly hypersensitivity reaction.
Poststreptococcal Glomerulonephritis: Immune reaction to group A beta-hemolytic streptococcal infection.
Onset:
Nephrotic Syndrome: Insidious.
Poststreptococcal Glomerulonephritis: Abrupt.
Urine Findings:
Nephrotic Syndrome: Proteinuria with mild hematuria.
Poststreptococcal Glomerulonephritis: Grossly bloody urine.
Edema:
Nephrotic Syndrome: Marked edema.
Poststreptococcal Glomerulonephritis: Mild.
Hypertension:
Nephrotic Syndrome: Rare to mild.
Poststreptococcal Glomerulonephritis: Marked.
Hyperlipidemia:
Nephrotic Syndrome: Extreme.
Poststreptococcal Glomerulonephritis: Rare.
Comparison #2: Additional Assessments
Peak Age Frequency:
Nephrotic Syndrome: 2-3 years.
Poststreptococcal Glomerulonephritis: 5-12 years.
Interventions:
Nephrotic Syndrome: Bed rest during edema phase; corticosteroids; immunosuppressants if needed.
Poststreptococcal Glomerulonephritis: Limited activity; antihypertensives as required; symptomatic therapy.
Diet:
Nephrotic Syndrome: High protein, low sodium.
Poststreptococcal Glomerulonephritis: Normal for age; reduced salt intake if hypertensive.
Prevention:
Nephrotic Syndrome: None known.
Poststreptococcal Glomerulonephritis: Treatment of group A beta-hemolytic streptococcal infections.
Question #2
Is the following statement true or false?
A presenting symptom for acute poststreptococcal glomerulonephritis is edema that moves depending on the position of the client.
Answer to Question #2
False
Edema that shifts with position is typically associated with nephrotic syndrome.
Nephrotic syndrome often presents with edema around the eyes and face on waking, which then progresses to other areas of the body as the child changes position.
Wilms Tumor (Nephroblastoma)
Overview:
Most common renal malignancy in children and one of the most common abdominal tumors in early childhood.
Arises from remnant embryonic tissue that persists after birth.
Often has no symptoms other than an abdominal mass or swelling.
Upon diagnosis, clinicians must post signs to avoid abdominal palpation.
Treatment:
Surgical removal of the tumor and affected kidney as soon as possible, followed by radiation and chemotherapy.
Prognosis:
Dependent on the stage and extent of the disease.
Hydrocele
Description:
Collection of peritoneal fluid that occupies the scrotum through a small, fingerlike projection in the inguinal canal, facilitating the descent of the testes.
The processus requires closure shortly after birth, and if it fails to close, peritoneal fluid can accumulate, resulting in hydrocele.
If hydrocele persists by the end of the first year, corrective surgery is performed.
Cryptorchidism
Definition:
Refers to the condition where one or both testes do not descend into the scrotum shortly before or after birth.
The testes are typically normal in size, but the exact cause remains unclear.
If both testes remain undescended, it can lead to:
Sterility
Increased risk for testicular cancer.
Surgical correction known as orchidopexy is often performed when the child is 1 to 2 years old.
Prognosis is generally good.
Menstrual Disorders #1
Menarche:
Refers to the beginning of menstruation, typically occurring between ages 9 and 16.
Irregular menstruation is common during the first year.
Mittelschmerz:
Described as dull, aching abdominal pain during ovulation, typically alleviated by analgesics, heating pads, or warm baths.
Each individual may experience this differently.
Menstrual Disorders #2
Premenstrual Syndrome (PMS):
Symptoms include:
Edema
Headache
Increased anxiety
Mild depression
Mood swings
The exact cause remains unknown, but it may be linked to hormonal changes.
Symptoms are often mild and may be alleviated by lifestyle changes.
Treatment Options:
Dietary supplements
Vitamins
Herbal preparations
Mild analgesics
Application of local heat
Mild diuretics
Oral contraceptive pills.
Menstrual Disorders #3
Dysmenorrhea:
Classified as:
Primary Dysmenorrhea: Part of the normal menstrual cycle without associated pelvic disease.
Secondary Dysmenorrhea: Resulting from pelvic pathologic changes, such as pelvic inflammatory disease (PID), fibroids, or endometriosis.
Symptoms:
Cramping abdominal pain
Leg pain
Backache
Treatment varies depending on the cause; NSAIDs are effective for primary dysmenorrhea.
Menstrual Disorders #4
Amenorrhea:
Primary Amenorrhea: Refers to a lack of menstruation after age 16; requires diagnostic evaluation for genetic or other abnormalities.
Secondary Amenorrhea: Defined as missing 3 or more periods after menarche; can result from discontinuation of contraceptives, pregnancy, physical or emotional stressors, or underlying medical conditions.
A complete physical examination is necessary to ascertain cause.
Vaginitis
Causes:
Associated with various factors including prolonged use of diaphragms or tampons, irritating douches or sprays, hormonal changes from birth control pills, and antibiotic treatment; these can increase the risk for infectious organisms.
Common Pathogens:
Candida albicans
Gardnerella vaginalis
Trichomonas, which is a sexually transmitted infection (STI).
Question #3
What is a recognized symptom of premenstrual syndrome?
a. Intense itching
b. Severe abdominal pain
c. Weight loss
d. Increased anxiety
Answer to Question #3
d. Increased anxiety
Rationale: Symptoms of premenstrual syndrome include edema leading to weight gain, headaches, increased anxiety, mild depression, and mood swings.