Test-2 Respiratory Flashcards
(84 cards)
Breathing remains primarily nasal until
5-6 months of age
Infants normally breathe with an
Irregular rhythm
Children breathe
Abdominally and diaphragmatically
Chest radiograph
X ray
See respiratory disease in lungs
CT scan
See tumors and large masses
Bronchoscopy
Biopsy of lung tissue/lesion, remove foreign tissue
Laryngoscopy
Direct view of larynx . Diagnosis of stridor
PULMONARY function testing
Spirometer direct measure of vital capacity and expiratory flow rate
Sputum cultures
Isolate pathogens
Transcutaneous monitoring
Electrode used to detect O2 and co2 concentrations
Cystic fibrosis
Inherited progressive autosomal recessive disorder affecting cells that produce mucous, sweat and digestive juices
People with cystic fibrosis
Have inherited two copies of the defective CF gene-one from each parent
Cystic fibrosis cause
Gene changes. Protein that regulates movement of salt in and out of cells
Cystic fibrosis results
Abnormal accumulation of thick, sticky mucus. Leads to obstruction in pancreas, respiratory, GI and GU systems
Cystic fibrosis in the respiratory system
Chronic infection, inflammation, bronchispasms Impaired has exchange Hypoxia Increased vascular resistance Heart pumps harder CHF
Cystic fibrosis early manifestation
Wheezing
Dry, non productive cough
Frequent respiratory infections
Cystic fibrosis late manifestations
Digital clubbing
Barrel chest
Nasal polyps
Cystic fibrosis digestive system pancreas
Mucus prevents release of digestive enzymes that allow body to break down food
Diabetes type 1
Bowel obstruction
Poor absorption of proteins, cholesterol, fats
Cystic fibrosis digestive
Bowel
Fecal impaction Intussusception Meconium ileus in newborn Recap prolapse Steatorrhea Growth retardation Delayed bone age
Cystic fibrosis physical manifestations
Protuberant abdomen
Wasted buttocks
Thin extremities
Chaotic fibrosis and skin
Parent may report salty taste when kissing infant
Xerostoma
Increased sodium and chloride in sweat
Cystic fibrosis reproductive system
Males are sterile
Females- fertility problems
Cystic fibrosis Dx and tests
DNA screenings Family history Clinical signs Pilocarpine lontophoresis (sweat test) Measures Na and Cl > 60mEq/l is diagnostic
Additional tests for cystic fibrosis
72 hour fecal fat Liver function Fasting glucose Chest X ray Sputum PULMONARY function