Exam 3 Peds GU Flashcards

(41 cards)

1
Q

Anatomical and physiological differences between children and adults

A

Urinary concentration
Structural differences
Urine output
Reproductive organ maturity

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Opening of the urethra is on the ventral surface of the penis

A

Hypospadias

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Opening of the urethra is on the dorsal surface of the penis

A

Epispadias

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

When is hypo/epispadias surgically repaired?

A

By 1 year

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Assessment for hypo/epispadias

A

Insepct penis for placement of urethre
Chordee
Palpate for presence of testicles

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Routine post-operative care for hypo/epispadias

A

Foley – be sure is secured in order to not place stress on incisions
Antibiotics, pain medications, anti-spasmodics
Double diaper

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

UTI

A

Occurs due to bacteria ascending to the bladder from the urethra
Most common serious bacterial infection in children

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Who is at the highest risk for a UTI?

A

Infants and young children
Until age 1 more common in males than females
Then more common in females than males

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Presentation of UTIs in children

A

Poor appetite, enuresis, frequent urination, fatigue, blood in urine, painful urination, abdominal or back pain

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Presentation of UTIs in infants

A

Poor feeding or vomiting, screaming on urination, fever, strong smelling urine, persistent diaper rash, dehydration

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

UTI pathogens

A

E. Coli (80%)
Klebsiella
Staph
Pseudomonas

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Causes of UTIs

A
#1 is urinary stasis
Decrease fluid intake
Alkaline urine
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Lab and Diagnosis tests for UTIs

A

Urinalysis (UA)
Urine culture
Renal ultrasound
VCUG

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Nursing interventions for UTIs

A

Administer antibiotics to eliminate infection
Surgery correction if cause is anatomic defect
Encourage PO intake or IVF – avoid cola or caffeine
Urinate frequently, empty bladder completely
Promote hygiene
No bubble baths, cotton underwear, to tight pants, wipe from front to back, wash area daily with soap and water
Teenagers  educate to void after intercourse
Administer antipyretics if needed, heating pad
Educate parents on how to prevent recurrent infection

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Vesicoureteral Reflux

A

Urine from the bladder flows back up the ureters
Occurs with bladder contraction during voiding
After voiding goes back into bladder is a great place for bacterial growth until next void  leads to kidney infections

Can lead to renal scarring and hypertension

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Signs and symptoms for assessing Vesicoureteral reflux

A
Fever
Dysuria or hematuria
Frequency or urgency
Nocturia
Back or abdominal pain
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Physical exam for Vesicoureteral reflux

A
Monitor BP (could be elevated)
Palpate abdomen for hydronephrosis
History of frequent UTIs? Congenital defects?
18
Q

Nursing interventions for Vesicoureteral Reflux

A

Antibiotic prophylaxis
Proper hygiene/voiding practices
Serial urine cultures (every 2-3 months and with fevers) and annual VCUG to assess progression of reflux
Many children will outgrow over a period of years

19
Q

Goal of vesicoureteral reflux management

A

To prevent pyelonephrosis and renal scarring

20
Q

When does vesicoureteral reflux require surgical intervention?

A

For grade 3-5

21
Q

Obstructive uropathy

A

An obstruction at any level along the upper or lower urinary tract that blocks the normal flow of urine

22
Q

What can obstructive uropathy lead to?

A

Dilation of the affected kidney (hydronephrosis) and ureter
Recurrent UTI
Renal insufficiency
Progressive damage to kidney

23
Q

Common signs and symptoms of obstructive uropathy

A
Recurrent UTI
Incontinence
Fever
Flank pain
Urinary frequency 
Hematuria
24
Q

Postop care for surgical correction of obstructive uropathy

A

Monitor UOP
Encourage PO or IVF
Pain meds or antispasmodics
Educate parents

25
What to monitor with obstructive uropathy
Palpate abdomen for masses | Monitor BP
26
A clinical state that occurs as a result of increased glomerular basement membrane permeability to plasma proteins Allows abnormal loss of protein in the urine
Nephrotic Syndrome
27
3 forms of nephrotic syndrome
Congenital Idiopathic (80%) Secondary
28
Speculated Causes of Idiopathic nephrotic syndrome
Metabolic Biochemical, physiochemical Immune-mediated response
29
Patho of nephrotic syndrome
Increased glomerular permeability allows passage of larger plasma proteins through the glomerular basement membrane Results in an excess loss of protein (albumin) in the urine (proteinuria) Have a decreased amount of protein in blood (hypoalbuminemia) Causes a change in osmotic pressure and fluid shifts from bloodstream into interstitial fluid, edema (especially the abdominal cavity, called ascites) Lowers blood volume (hypovolemia) which “starves” kidneys, they hold on to Na and H2O, more edema Liver senses the protein loss and increases production of lipoproteins Results in hyperlipidemia because lipids cannot be excrete in urine At increased risk for clotting because of decreased intravascular volume Also at increased risk for infection or renal failure Diagnosis: Clinical manifestations (especially weight gain), labs
30
Common signs and symptoms of nephrotic syndrome
Recent wt gain History of periorbital edema when awakening then generalized edema during day Abdominal swelling (ascites) Pleural effusion, labia or scrotal swelling Weakness or irritability Decreased urine volume, frothy Susceptible to infection
31
Physical exam for nephrotic syndrome
Edema BP – normal or slightly decreased Heart and lung sounds Palpate skin and abdomen
32
Lab and Diagnostic tests for nephrotic syndrome
Clinical manifestations: Urinalysis Marked proteinuria Mild hematuria, if any Serum protein and albumin levels low Serum cholesterol and triglyceride levels elevated Eventually BUN and Cr will become elevated Renal biopsy done if does not respond to treatment
33
Management objectives for nephrotic syndrome
Reducing excretion of urinary protein Reducing fluid retention Preventing infection Minimizing complications related to therapies
34
Diet for nephrotic syndrome
Low salt diet, possible fluid restriction
35
Meds for nephrotic syndrome
If edema is severe – diuretics and albumin Infection - abx Corticosteroids – 1st line of therapy for NS Prednisone for 21 days then taper off About 2/3 will relapse Repeat course of steroid therapy or other immunosuppressive meds May last for many years
36
Continued monitoring for nephrotic syndrome
``` Continuous monitoring of fluid retention or excretion Strict I & O Daily weight Measure abd girth In-depth skin assessment Monitor VS Protect against infection Promote adequate nutrition Protein rich snacks ```
37
Parent education for nephrotic syndrome
``` Signs of relapse Urine dipstick at home Prevent infection but CAN go to school Mood swings related to steroids Emotional toll of relapse ```
38
Acute Glomerulonephritis
Immune complexes are deposited in the glomerular basement membrane Causes inflammation and edema due to leukocytes Altered glomerular structure and function in both kidneys (cannot filter properly) Results in excessive amounts of water and retention of Na  expands plasma and interstitial fluid volumes  circulatory congestion (HTN) and edema
39
When does Acute Glomerulonephritis usually occur?
After an infection Acute post streptococcal glomerulonephritis (Group A ß-hemolytic streptococcus) Latent period of 10-21 days after infection
40
Acute Glomerulonephritis clinical manifestations
Edema – periorbital and then spreads to extremities and abdomen Gross hematuria – causes discoloration of urine (cloudy, smoky brown like cola or tea) Mild proteinuria Severely reduced urine volume Mild to moderately elevated blood pressure (HA) Pallor, irritability, lethargy, anorexia, child appears ill Diagnosed with + antistreptolysin O (ASO) titer Might have a CXR (cardiac enlargement, pulmonary congestion, pleural effusion) during the edematous phase
41
Diagnosis and treatment of Acute Glomerulonephritis
Diagnosed with + antistreptolysin O (ASO) titer and clinical manifestations Might have a CXR (cardiac enlargement, pulmonary congestion, pleural effusion) during the edematous phase No treatment – just supportive measures Diet – moderate sodium restriction, possible fluid restriction if severe edema, K restriction during oliguric phase Measure VS, wt, strict I & O Determine HTN early and give antihypertensives or diuretics Give abx if strep is still positive Daily wt is the best way to assess fluid balance Bed rest during acute phase then allow frequent rest periods