Care of the Pediatric Patient with Elimination Problems
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Transcript Care of the Pediatric Patient with Elimination Problems
Care of the Pediatric
Patient with Elimination
Problems
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Elizabeth Allen RN, MSN
Identify anatomic and physiologic differences
between the adult & pediatric renal system
Describe pathologic conditions of the renal
system in the pediatric patient
Discuss treatment, testing and specimen
collection for a UTI in a pediatric patient
Learning Objectives
Kidneys less efficient until 2 years
Kidney grow most in first 5 years
Bladder capacity increases with age
Bladder capacity age + 2 in oz.
Bladder control >2 years due to nerve
development
Low set ears associated with urinary tract
abnormalities
Anatomic and Physiologic
Differences
Gomerulonephritis
Acute Post-infectious Gomerulonephritis
Most often results from Strep infection on skin
(impetigo) or throat
Also from staphylococcus, Pneumococcus and
Coxsackie
Develops 10-21 days post infection
Most common 2-6 years
Renal
Gomerulonephritis
Immune complex Reaction
Renal
Antigen-Antibody complexes lodge in glomeruli
Inflammation and Obstruction
Increased permeability to RBCs & Protein
Decreased ability to filter wastes, regulate fluid
balance
Glomerulonephritis
Symptoms
Renal
Hematuria
Mild to Moderate
Proteinuria
Elevated BUN,
Creatinine
Fever
Flank or midabdominal
Pain
Edema- periorbital and
dependent
Acute HTN- possible
encephalopathy and
headache from HTN
Hypertension: defined by percentiles for Age &
Height per National Heart Lung and Blood
Institute
Hypertension is defined as a reading >95th
percentile for children of similar gender, age and
height
http://www.nhlbi.nih.gov/files/docs/guidelines/
child_tbl.pdf
Renal- Definition of HTN
Glomerulonephritis
Treatment
Acute Phase
Risk for infection
Risk for skin breakdown
Fluid and electrolyte correction
Renal
Monitor urine output
Fluid restriction
Low protein, low sodium diet
Treat HTN, pain
Antibiotic for infection
Dialysis as needed
Resolves 3 weeks or longer
Nephrotic Syndrome
Clinical State: Increased protein
permeability in glomeruli
85% have Minimal Change Nephrotic
Syndrome (MCNS)
Congenital
Primary (i.e. glomerulonephritis)
Secondary (disease, drugs, toxins)
Renal
Nephrotic Syndrome Signs
Edema
Massive Proteinuria- frothy urine!
Altered immunity
Hyperlipidemia
Hypoalbuminemia, hypoproteinemia
Hypercoagulability
Renal
Nephrotic Syndrome Treatment
Corticosteroid
Risk for Skin Breakdown
Risk for Infection
Treat Pain
IV Albumin and Furosemide to reduce
edema
Renal
Renal
National Kidney and Urologic Diseases
Information Clearinghouse (NKUDIC)
Resource for Nephrotic Syndrome
http://kidney.niddk.nih.gov/KUDiseases/pubs/c
hildkidneydiseases/nephrotic_syndrom/#sec8
Polycystic Kidney Disease
Genetic Disorder
Autosomal dominant and recessive
Cysts form in collecting ducts- become
larger as child grows
Cysts replace kidney mass and reduce
function
Cysts also develop in liver
Renal
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Autosomal Dominant
90% of PKD
Symptoms usually
develop age 30-40,
can begin in
childhood
Symptoms of Renal
Failure
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Autosomal Recessive
Rare
Symptoms start
perinatally to 1 year
Low set ears, small
jaw, flat nose
Symptoms
Renal
HTN
UTIs
Oliguria
Respiratory Distress
Developmental Delay
Liver problems
Treatment is
supportive
Wilm’s Tumor (Nephroblastoma)
Most often 2-3 years
Palpable mass on 1 side or other abdomen
Fast growing- doubles in size in 11-13 days
Staging of tumor
Preoperatively, do not palpate after diagnosis
Do not know what stage/lymph involvement
Renal
Wilm’s Tumor Treatment
Nephrectomy- involved kidney only
Post op care of patient
Chemotherapy or Radiation as needed
for Staging
Single Kidney
Renal
http://www.healthychildren.org/English/healthissues/conditions/genitourinarytract/Pages/Children-with-a-Single-Kidney.aspx
Urinary Tract Infections
0-6 months more common in boys
Especially uncircumcised males
>2 years more common in girls
Cystitis and pyelonephritis
Urinary
UTI
Specimen collection
Sterile: straight cath in non toilet trained
Clean catch: hat for toilet trained
VCUG (Voiding cystourethrogram) for
repeated UTIs
Renal Ultrasound
Treatment with Antibiotics
Education for parents or patient
http://www.healthychildren.org/English/agesstages/baby/bathing-skin-care/Pages/Care-for-anUncircumcised-Penis.aspx
Urinary
Congenital Urinary Tract Disorders
Increased risk for Latex Allergy
Usually require surgical correction
Neurogenic bladder: may result from congenital
defect affecting spinal cord or acquired condition
Urinary
Hypospadias
Congenital
Hypospadias may be anywhere on
ventral shaft of penis
Associated with Chordee
Surgical repair < 1 year
Delay circumcision
Urinary
Hypospadias
Post Op Care
Urinary catheter or stent stitched in place
Double diapering or dressing to protect
stent
Pain management
Restricted activity
Monitor urine output
Urinary
Enuresis
Nocturnal or diurnal
Primary or Secondary
Thorough assessment including family hx
Strategies to promote dryness
Evening fluid restriction
Positive rewards
Waking to void
Alarms
Pharmacological approach
Urinary
Encopresis
Stool holding or soiling at inappropriate times
Primary or secondary
Retention of stool in rectum- becomes hard and
painful
Leads to irregular/unpredictable elimination
pattern
Liquid stool may ooze around it
Often present as constipation or diarrhea
Bowel
Encopresis
Studies to rule out disorder
Evacuate bowel- enema
Dietary management of constipation
Positive reinforcement
Toileting schedule
Bowel