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53 Cards in this Set

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  • Back
List the four medications used of UTI's in Pediatrics
1. TMP-SMX
2. Amoxicillin
3. Cephalexin
4. Pyridium (OTC)
Trimethoprim-Sulfamethoxazole (TMP-SMX)
Class- anti-infective, antiprotozols (Pharm) folate antagonist, sulfonamides
Rout: PO, IV
Action: inhibits metabolism of folic acid in bacteria. Active against both gram +/-
Take all, Notify PHC if fever and diarreha develp. Protect agianst sun
Amoxicillin
Class- anti-infective (pharm) aminopenicillins
Action- bind to bacteria cell wall, causing death
side effects- rashes, diarrhea, may increase warfarin effectiveness and decrease BC effectiveness
Route- PO only (chewable, caps, suspension
>3 mo 25-50mg/kg/day divided in 8-12 hr doses
< 3 mo 20-30 mg/kg/day
Monitor bowel function, may cause false coombs test
Cephalexin
Class: anti-infective
Action: treatment of infection caused by susceptable organism, binds to bacteria and causes cell death. Active against most gram +, selective gram -
Route: PO, IM, IV
15mg/kg/day
Side effects: N&V, diarrhea, rashes, pain and plebitis at IV site.
Caution in renal impairment , GI disease, if taken with loop diuretic or aminoglycosides may increase renal toxicity
Pyridium (OTC)
Class: nonopioid analgesic (pharm) Urinar tract analgesic
Action: provides relief from UT symptoms; pain, burning, itching, urinary frequency
Route: PO only (DONT Crush/Break)
4mg/kg 3x daily for 2 days
side effects: bright red-orange urine
Use caution in hepatitis pts, also interfers with urine tests that are based on color reaction
Nephrotic Syndrome management
Diet: low to moderate protein, Na restriction with large amounts of edema
Steroids: 2 mg/kg divided dose bid (prednisone is the drug of choice)
Immunosuppressant therapy (cytoxan)
low-dose, Long term antibiotics to prevent relapse
Diuretics if severe
Possible do renal biopsy
Types of Glomerulonephritis
Most are postinfectious
Pneumococcal, streptococcal, or viral
May be distinct entity or
May be a manifestation of systemic disorder
Systemic lupus erythematosus
Sickle cell disease
Others
Glomerulonephritis Symptoms
Hematuria
Bleeding in upper urinary tract→smoky urine
Proteinuria
Increased amount of protein = increased severity of renal disease
Investigation of Acute Glomerulonephritis for the Following
Generalized edema caused by decreased glomerular filtration
Begins with periorbital edema
Loss of appetite
Decreased urinary output
Progresses to lower extremities and then to ascites
Cola or tea-colored urine
Prognosis of Glomerulonephritis
Almost all children diagnosed with acute poststreptococcal glomerulonephritis recover completely
Specific immunity is conferred
Subsequent recurrences are uncommon
Some children have been reported to develop chronic disease
Nursing Care Management of Glomulonephritis
Manage edema
Daily weights
Accurate input and output
Daily abdominal girth
Nutrition
Low sodium, low-to-moderate protein
Susceptibility to infections
Bed rest is not always necessary
Wilms’ Tumor
Also called nephroblastoma
Malignant renal and intraabdominal tumor of childhood
Three times more common in African-American children
Peak age of diagnosis is 3 years
More frequent in males
Bladder capasity of newborns and childrens
NB
30-60 mL
Children
oz= age (years) +2
for example a two year old would be 2+2= 4 oz
Specific gravity
NB= 1.001- 1.020
Everyone else= 1.001= 1.003
High= dehydration, presence of protien or glucose or presence of medium contrast
Low= excessive fluid intake, distal tubal disfunction, insufficient antidiuretic hormone, diuresis
pH
NB= 5-7
everyone else= 4.8-7.8
acid or neutral= associated with metabolic acidosis, suggest tubular acidosis if associated with metabolic alkalosis, suggest potassium deficiency urinary infection
alkaline= metabolic alkolosis
Glucose level
should be absent
if present= DM, infusin of glucose containing fluid, Glomerulunephritis, impaired tubular reabsorption
Ketones
should be absent
if present= acute metabolic demand (stress) diabetic ketoacidosis
Leukocyte esterase
should be absent
if present= can identify both lysed and intact WBC via enzyme detection
Nitrites
shout be absent
if present= most species of bacteria convert nitrates to nitrites in the urine
WBC count
Normal = < 1 or 2
> 5= polymorphonuclear- UTI process leukocyte/field
RBC count
normal= < 1 or 2
greater= trauma, stones, glomerular injury, infection, neoplasms
Cast
normal - occassional
granulare cast- tubular or glomerula disorder, advanced renal disease
cellular cast- pyelonephritis
WBC- glomerulonephritis
RBC- protienuria, usually transient hyaline
BUN
Blood Urea Nitrogen
NB= 4-18
infant, child= 5-18
elevated= renal disease, dehydration, hemorrhage, increase protein intake, corticosteroid therapy
Creatine
infant- 0.2-0.4
child - 0.3-0.7
Adolescent- 0.5-1.0
increased= severe renal impairment
Cystitis

Pyleonephritis
Cystitis- inflammation of the bladder
pyelonephritis- inflammation of the upper urinary track and kidneys
Types of UTIs
Recurrent: repeated episodes
Persistent: bacteriuria despite antibiotics
Febrile: typically indicates pyelonephritis
Urosepsis: bacterial illness; urinary pathogens in blood
A variety of organisms are responsible for UTI
what is the most common
80% Escherichia coli
How much urine is produced per hr
NB will produce 1-2 ml/kg/hr; after 1 month, approximately 1 ml/kg/hr
UTI Clinical Manifestations of neonate
Poor feeding, vomiting
Failure to gain weight
Respiratory distress
Frequent urination
Screaming on urination
Jaundice, dehydration
UTI Clinical Manifestations of infants
Poor feeding, vomiting
Failure to thrive
Excessive thirst
Frequent urination
Foul-smelling urine
Pallor, fever
Persistent diaper rash
UTI Clinical Manifestations of a child
Poor appetite, vomiting
Growth failure
Excessive thirst
Enuresis, incontinence
Swelling of face, pallor
Fatigue, abdominal or back pain
Blood in urine
Classification of UTI
Upper tract: involves renal parenchyma, pelvis, and ureters
Typically causes fever, chills, flank pain
Lower tract: involves lower urinary tract
Usually no systemic manifestations
Lower tract

Upper tract
Lower tract- Cystitis, Urethritis

Upper tract, Pyelonephritis, VUR, Glomerulonephritis
Diagnostic Studies of UTI
Clean-catch is preferred
U-bag for collection from child
Specimen obtained by catheterization or suprapubic needle aspiration has more accurate results -May be necessary when clean-catch cannot be obtained
Vesicoureteral Reflex
primary vs secondary
Primary reflux
Congenitally abnormal insertion of the ureters into the bladder
Secondary reflux
Result of an acquired condition
Vesicoureteral Reflux
Abnormal retrograde flow of bladder urine into the ureters
Reflux often associated with a UTI in which the child has a high fever, vomiting and chills
Renal scarring can occur from the reflux and should be prevented.
Therapy: low dose daily antibiotic therapy
Nursing considerations:Instruct parents to watch for signs and symptoms of UTI. Prevent recurrent infections. Education on diagnostic procedures.
Etiology and Pathophysiology of Acute Pyelonephritis
Inflammation caused by bacteria, fungi, protozoa, or viruses infecting kidneys
Urosepsis: systemic infection from urologic source
Can lead to septic shock and death in 15% of cases
Preexisting factor (usually)
Vesicoureteral reflux
Dysfunction of lower urinary tract function -Obstruction- Stricture
Clinical Manifestations of Acute Pyelonephritis
Vary from mild to “classic” and very severe
Presenting symptoms
N/V, anorexia, chills, nocturia, frequency, urgency
Suprapubic or low back pain, dysuria
Fever, hematuria, foul-smelling urine
Costovertebral tenderness
Symptoms often subside in a few days, even without therapy
Bacteriuria and pyuria still persist
Diagnostic Studies of Acute Pyelonephritis
Urinalysis
WBC casts
CBC
Imaging studies (IVP or CT)
Ultrasound
Obstructive Uropathy
Structural or functional abnormalities that obstruct normal flow
Back up of the urine above the obstruction causes hydronephrosis
Acquired, unilateral, bilateral, complete or incomplete
Early diagnosis and surgical correction is essential
Hydronephrosis
Dilation of the renal pelvis from distention
Obstructions can be congenital or acquired, unilateral or bilateral, complete or incomplete, or acute or chronic.
Needs early diagnosis and evaluation
Nursing considerations for Hydronephrosis
Help identify cases
Assist with diagnostic procedures
Care for children with complications
Emotional support and counseling
Education on ureteral drainage systems
Some may face challenges with dialysis or transplantation
Nephrotic Syndrome
Most common presentation of glomerular injury in children
Characteristics (key)
Proteinuria- loss of protien in urine
Hypoalbuminemia- all of albuminem is going out through urine
Hyperlipidemia
Edema- fluid going from intervascular to interstitual
Massive urinary protein loss
Types of Nephrotic Syndrome
Minimal change nephrotic syndrome
AKA
Idiopathic nephrosis
Childhood nephrosis
Minimal lesion nephrosis
Secondary nephrotic syndrome
Congenital nephrotic syndrome
Autosomal recessive disorder
Age 2-7, more common in boys
Changes in Nephrotic Syndrome
Glomerular membrane
Normally impermeable to large proteins
Becomes permeable to proteins, especially albumin
Albumin lost in urine (hyperalbuminuria)
Serum albumin decreased (hypoalbuminemia)
Fluid shifts from plasma to interstitial spaces
Wilms Tumor Clinical Manifestations:
Abdominal mass; increased abdominal girth
Anorexia and malaise
Nausea and vomiting
Elevated blood pressure
Hematuria (late and grave symptom)
Weight loss
Fever
Alterations r/t metastasis to lungs
Defects of the Genitourinary Tract
Hydrocele-abnormal fluid in scrotum
Phimosis- tight foreskin around the penis
Hypospadias- urethra under penis
Chordee- curvature to penis
Epispadias- urethra above penis
Cryptorchidism- fail of testes to descend one or both
Phimosis
Narrowing or stenosis of preputial opening of foreskin
Therapy: manual retraction or circumcision
Hypospadias
Urethral opening located behind glans penis or anywhere along ventral surface of the shaft
Treatment: surgical correction to provide direct stream on voiding
Nursing care: Education pre and postop expectations
Chordee
Ventral curvature of penis, often associated with hypospadias
-caused by fibrous bands on the penis that causes the glan penis to be pulled ventrally
Treatment: surgical release of fibrous bands
Cryptorchidism
Failure or one or both testes to descend normally through inguinal canal
Treatment: admininstration of HCG or surgical orchiopexy
Nursing considerations: Education pre and postop procedures and expectations
Epispadias
Location of the urethral opening on the dorsal surface of the penis
Treatment: surgical procedure- lengthening of penis and urethra and possibly reconstruction of bladder neck
Enuresis (aka bedwetting)
Intentional or involuntary passage of urine into the bed or clothes when passed the age voluntary bladder should have been achieved.
Diagnosed past age 5yrs when involuntary voiding occurs at least twice a week for at least 3 months.
More common in boys
Nocturnal bedwetting should stop between 6-8 years of age.
Management: drugs (DDAVP and Tofranil), bladder training, elimination of evening fluids, waking to void at night, electrical devices to waken the child upon voiding.