Fluid & Electrolyte
GI Alterations
Nursing 355
Maria Rubolino-Gallego
Distribution of Body Fluids in Pediatrics
n Children are more vulnerable than adults to changes in electrolyte balance
n Sensible water loss vs. insensible water loss
n Infants have a higher % of water in their extracellular fluid
n Approx. 40% of body water is in the ECF in a neonate compared with 25% at age 2 and 20% in adults
n Infants and young children unable to verbalize thirst
n Water is located in two major compartments
- Intracellular
- Extracellular
Proportion of water contents:
90% of premature infants
75-80% of full-term infants
60-65% of preschool children
55-60% of adolescents and adults
Review of Mechanisms of Fluid Movement
n Hydrostatic pressure
n Osmotic pressure
n Diffusion-mvmt of molecules from higher conc. to regions of lesser conc.
n Active transport
Water Balance in Infants
n Surface area – greater amounts in premature infants
n Metabolic rate – greater in infants
n Kidney function –immature and unable to concentrate urine
n Fluid requirements – ingest and excrete a greater amount of fluid per kg of body weight
n Little fluid reserve
Fluid and Electrolyte Disorders
n Hyponatremia – less than 150mEq/L
n Causes of this:
n Sxs: HA, dizziness
n Hypernatremia – over 150mEq/L
n Causes of this:
n Sxs: Thirst, oliguria
Assessment of Fluid/Electrolyte Disturbances
n Tissue turgor –
– Poor with dehydration
n Mucous membranes –
– dry to slightly moist
n Vital signs – afebrile to febrile, tachycardia
n Weight changes –
– loss is related to fluid defici
– gain is related to edema or ascites
n Urine volume and concentration – usually diminished to oliguria depending on the severity of fluid deficit
n Specific gravity
– Low due to: fluid excess, sodium deficit
– High due to: fluid deficit, sodium excess
n Sensory changes
– Tingling in fingers and toes
– Abdominal cramps
– Muscles cramps
– Light-headedness
– Nausea
– Thirst
n Neurological changes:
– Hypotonia
– Flaccid
– Weakness
– Hypertonia
– Tremors
– Cramps
– Twitching
Fontanel's – what happens to them?
Dehydration
n Isonatremic – water and electrolytes lost in equal amounts and sodium serum levels is normal (135-145 mEq/L)
n Most common type
n Hyponatremic – Loss of electrolytes greater than water loss, sodium conc. of less than 130
n Hypenatremic –Loss of water greater than electrolytes loss, sodium serum concentration is above 150
n Causes-
Degree of Dehydration
n Mild – 4-5% loss of body weight; fluid volume loss of less than 50 ml/kg
n Moderate – 6-10% loss of body weight; fluid volume loss of 50-90 ml/kg
n Severe – 10% or more loss of body weight; fluid volume loss of 100 ml/kg or more
n Determine percent of dehydration
n 1 ml of body fluid is equal to 1 gm of body weight
Nursing Responsibilities in Children
n History – history of acute and chronic fluid loss, weight of child, stools, vomitus, diapers (wet/stool)
n Clinical observations – lethargy, confusion, or seizures, cry, skin color, fontanel, pulse, respirations, vital signs, tears, mucous membranes
n Laboratory values –
– check sodium, potassium, urine (including specific gravity), calcium
n Monitor I/O’s accurately
n Monitor child’s weight
n Oral Rehydration Therapy (ORT): preferred TX with mild to moderate dehydration
n Examples include Pedialyte, Infalyte, Rehydralyte
n ?Gatorade - high percentage of sugar and carbohydrates
n ORT - 1 teaspoon of ORT every minute to 120ml (4 ounces) every hour
n NEVER GIVE PLAIN WATER WITHOUT ELECTROLYTES
n May lead to water intoxication and edema
n ?BRAT diet, clear liquids etc….
Severe Dehydration
Unable to take fluids
n Parenteral fluid and electrolyte therapy should be initiated
n Goal: prevent shock
n LR or NS is fluid of choice
n Maintenance therapy: add dextrose to the solution/ potassium may also be added
n Potassium may be added once urine is adequate
n Always check dosage – may lead to lethal dose in a child, never IV push, give at a rate no faster than 1 mEq/kg/hr)
Assessment
n History
n General Observation
n Clinical Observation
n Specific tests/procedures
– I/O
– Weight
– Stool, vomitus -frequency, type, amounts, consistency
– Urine output and specific gravity
– Sweating
– Skin
– Fontanel
– VS
– Blood tests including CBC, Electrolytes BUN/Creatnine, blood cultures
Diarrhea
n One of the most common disorders in children
n US, children younger than 5 years old experience 20-35 million episodes of diarrhea per year
n Increase in the frequency, fluidity, and volume of stools
n May be acute or chronic
n Typically called gastroenteritis when caused by infection
n Viral gastroenteritis makes up for approx. 80% of all cases
n Different causes: Bacterial vs. viral vs. parasitic
n Can lead to dehydration, shock, electrolyte imbalance
n Signs/symptoms: skin texture, abdominal cramps, stool changes, heart rate changes, respiratory rate changes
Rotavirus
n Rotavirus - , fecal-oral route, the peak incidence occurs between 7 and 15 months of age, with approximately 0.8 episodes per child per year
n Children become most susceptible after 6 months of age when the protection afforded by maternal antibodies wanes
n By 15 months of age many have developed some protection after primary infection
n Almost all children get rotavirus at least once before they are three years old
Management of Diarrhea
n Restore fluids and electrolytes
n Handwashing
n Avoid beverages high in carbohydrates (Gatorade)
n Oral Rehydration Therapy begin within first 24 hours
n Early reintroduction of feeding
n Rice cereal for younger children
n Breast milk – evidence that it may reduce the duration of diarrhea by approx. half a day
n Eat every 3-4 hours
Management
n Bland foods: complex carbohydrates
– Rice
– Wheat
– Potatoes
– Yogurt
– Cooked vegetables
– Lean meats
– Avoid BRAT diet
Vomiting
n Forcible ejection of stomach contents through the mouth
n Isolated incidents are of little concern, but persistent, prolonged vomiting can be serious
n Occurs frequently in children
n Causes: infections, motion sickness
n Diagnostic tests (if severe): CBC, electrolytes, blood cultures, glucose level, urine analysis
n Types:
– Greenish – bile or obstruction
– Fecal odor – lower intestinal obstruction or peritonitis
– Bright red blood- indicates that the blood has not been in contact with the gastric juices
Treatment of Vomiting
n Detecting and treating the underlying cause
n ORT
n Monitor electrolytes
n Monitor body weight
n IV therapy if severe or prolonged in neonates or young infants
n Antiemetics – Tigan, Phenergan
GI System
n Swallowing is not under voluntary control until 6 weeks
n Stomach capacity
– Newborn 10-20 ml
– 1 week 30-90 ml
– 1 month 90-150 ml
– 1 year 210-360 ml
– 2 years 500 ml
– Adult 200-3000 ml
Prenatal Development
n Gut is formed from the endoderm in the first 4 weeks of embryonic development
n Anatomically development is completed at birth
n Physiologically the neonates GI tract is immature
Disorders of Absorption and Digestion
n Lactose Intolerance
– Absence or deficiency of enzyme (lactase found in the small intestine)
– Unknown cause
– Increased incidence in 50-90% of Asian, Arabs, Jews, African American, and Southern Europeans
– Sxs: frothy diarrhea, abdominal distention and cramping, excessive flatus
– Usually seen by age 3
– Dx with stool which has 1+ or greater sugar or presumptive diagnosis
– Tx with lactose free diet (lacto free or soy formula)
Gastroesophageal Reflux
GERD
n Regurgitation of gastric contents back into the esophagus
n Causes: cerebral palsy, Down syndrome, head injury, obesity, hiatal hernia, also a normal phenomenon
n Typically resolves by 1-2 years of age
n Boys more affected than girls
n Preemies more affected than term infants
GERD
n Pathologic GERD - child can experience weight loss, failure to thrive, abdominal pain, irritability
n DX: Barium swallow, Upper GI study, pH studies, Ultrasound
n Treatment: Dietary alterations, positional changes, medications, surgery
GERD
n Diet: Small, frequent feedings of predigested formulas, frequent burping, thickened formula
n Positioning: 30 degree head elevated prone or right side-lying
n Medications: FDA has not approved them but used frequently with pathologic jaundice: H2 receptor antagonists, PPIs, protonics
Celiac Disease
n The inability to digest gluten
n Failure to thrive by 9-12 months of age
n Gluten in the protein found in wheat, rye, barley, oats
n 1 in 1000 live births in the US
n 80-90% of children have the genetic marker HLA-B8, a known leukocyte antigen complex on chromosome 6
n Sxs: Diarrhea, failure to grow (below 25th percentile), abdominal distention (ascites), vomiting, anemia, muscle wasting
n Usually not seen until at 3-6 months of age
n Dx: serum antigliadin antibody of strip AGA test, single drop of blood and ELISA test is used
n Diagnosis supported with change in diet
n Tx with lifelong dietary management of gluten-free diet
Constipation
n Infrequent and difficult passage of dry, hard stools (assess frequency, intensity, and duration)
n A major concern is encopresis or fecal incontinence
n Symptoms: absence of stool, abdominal pain, cramping
Encopresis
n Soiling usually affects ages 3-7 years
n More likely in boys
n Repeated and involuntary defecation in a child with a normal rectum and colon
n Children often complain that soiling occurs without warning
n Many causes: diet, dehydration, decreased exercise, emotional stress, certain medications, pain from anal fissures, and excessive milk intake
n Dx – enlarged rectum on X-ray and also history
n Enemas to decrease impaction but need to limit this tx until after diagnosis is established
n Tx: diet, exercise
n Stool softeners
n Diet changes
n Increase water, fiber
n Bathroom for 5-10 minutes within 20-30 minutes after eating
n Positive reinforcement, behavioral charts
Congenital Aganglionic Megacolon or Hirschsprung’s Disease
n Absence of ganglion cells in the rectum, cannot pass stool through the rectum efficiently
n More often males than females (4:1)
n Higher incidence with Down’s syndrome
n Can vary from mild to severe (if severe, requires surgery)
n Newborn: mec? in first 24 hours of life
n Sxs: Delayed passage or absence of meconium stool in newborn, chronic constipation and small stool or ribbon-like stools, constipation that has been persistent since the neonatal period
n Tx:stool softeners, rectal irrigations, surgery
Irritable Bowel Syndrome
n Increased motility that leads to spasms and pain
n Stress and emotional factors are thought to be the most common cause
n Infants related to lactase deficiency
n Age 16 to 20 months, school age and adolescents – most common in toddlers and adolescents
n Girls affected more than boys
n Tends to occur in families with a history of other bowel disturbances
n Disorganized contractility leading to diarrhea and constipation
n Dx: Elimination of other major GI conditions
n Management: to reduce symptoms, well balanced, moderate fiber diet
n Avoid carbonated drink beverages
Intussesception
n Invagination of a section of the intestine into the distal bowel that causes obstruction
n 3 months to 6 years – generally affects young children and infants, more common in children with celiac disease or cystic fibrosis
n Cause: unknown, contributing factors: viral infections
n 1 to 4 per 1000 births
n Pediatric emergency
n Sxs: paroxysms of pain, palpable, abdominal mass, vomiting, bleeding, or current jelly stools, sausage shaped abdominal mass
n Dx:Ultrasound, barium enema
n Tx: Hydrostatic reduction with barium or air enema or ultrasound guided enema (if fails, then surgery)
Appendicitis
n Inflammation and infection of the veriform appendix (at the end of the cecum)
n Most common in early adolescence and early adulthood
n In most cases, no known cause
n Uncommon for children but if occurs, most often leads to perforation due to the difficulty in diagnosing
n Sxs:Pain progressing in intensity, McBurney’s, rebound tenderness, N/V, anorexia, diarrhea, constipation, fever, chills
n Dx: Increased WBC
n Tx: Appy, NPO, pain control, antibiotics, no heat, no laxatives, no enema
Inflammatory Bowel Disease
n Chronic inflammation condition of the small or large intestine
n Includes 2 distinct conditions: Chron’s and ulcerative colitis
n Ulcerative colitis – affects only the colon
n Chron’s – can affect all of the GI tract
n Unknown cause, several triggers identified
n Dx: colonoscopy, barium enema
n Sxs: Weight loss, diarrhea, vitamin deficiency, anemia
n Tx: medication – anti-inflammatory, antibiotics, immunosupressive therapy, ASA, steroids
n Meds: Remicade – binds to tumor necrosis factor and will reduce inflammation
n Malnutrition is a common problem
n Remission and exacerbations are common
Necrotizing Enterocolitis
NEC
n Most common GI tract disorder in the neonate
n Necrotic lesions of the mucosa of the small and large intestine
n 1% - 15% of all infants admitted to NICU
n Incidence increases with decreasing gestational age
n S/S: apnea, bradycardia, temperature instability, emesis, bloody stools, visible bowel loops, abdominal tenderness
NEC
n DX: Xray reveals dilated bowel loops, air within the intestinal wall
n Labs: increased or decreased WBCs, decreased platelets, electrolyte imbalances
n Prevention: Breast milk (IgA and IgG), oral immunoglobulin
n Tx: decompression of the GI tract with NG tube, control sepsis, IV fluids, TPN
Pyloric Stenosis
n Circular area of muscle surrounding the pylorus hypertrophies and obstructs gastric emptying
n Most common surgical disorders in early infancy
n 3 in 1000 births
n Males more than females
n Full term infants are affected more often
Pyloric Stenosis
n Progressive projectile, nonbilious vomiting in a previously healthy infant
n Movable, palpable, firm, olive-shaped mass is felt in the RUQ
n DX: vomiting history, Xray, Ultrasound
n TX: Pyloromyotomy (release the obstruction)
Infectious Gastroenteritis
n Caused by a group of viruses, bacteria, or parasites
n High-risk groups – preschools, daycare, long-term care facilities
n Giardia – most common in daycare settings
n Rotavirus – most common in infants and young children
n Most common outpatient infectious diseases in children
n Peak in the summer
n Transmission- fecal-oral, food or water born
n Sxs: diarrhea, vomiting, abdominal pain, fever
n Tx: replace fluids correctly (IV or PO)
Biliary Atresia
n Obstruction or absence of the extrahepatic bile ducts
n Problem originates in the prenatal period (toxins, viruses, chemicals?)
n 1 in 10,00-20,000 births
n Will lead to cellular damage in the liver and eventually to liver failure
n Slightly higher incidence in females over males
n Sxs: child is healthy at birth, light colored stools, hepatomegaly
n Dx:LFTs, PT, PTT
n Tx: hepatic portoenterostomy to allow bile to drain from the liver, liver transplant
Viral Hepatitis
n Caused by different viruses
n Acute or chronic inflammation of the liver
n Hep A – common in daycare settings, highly contagious
n Hep B – perinatal transmission, blood transfusion, exposure to contaminated body fluids (can survive in the dry state for 1 wk)
Hep A
n Sxs: in A are often asymptomatic or mild
n Non-specific: anorexia, malaise, fatigability
n No specific treatment
n Handwashing
n Vaccine developed for this
Hep B
n Sxs
– Anicteric phase (without jaundice):
§ Anorexia
§ N/V
§ RUQ pain
§ Fever
§ Malaise
§ Depression
§ Fatigue
§ Irritability
§ Lasts 5-7 days
Hep B
n Sxs
– Icteric Phase (jaundiced)
§ Jaundice
§ Urticaria
§ Dark urine
§ Light colored stools
Hep B
n Hep B vaccine in infancy
n Recommended to begin vaccination series in the hospital as a newborn