Final Flashcards
platelet coagulate. increased capillary permeability. Migration of neutrophils and monocytes to eat debris and destroy bacteria
inflammatory phase
2-3 weeks post injury. collagen synthesis. Epithelialization. Delayed if too wet or too dry
proliferative phase
scar maturation. can take up to 18 months
remodeling phase
Mild pain meds (2)
- NSAIDS
2. Acetaminophen
Moderate pain meds (2)
- Codeine
2. oxycodone
Severe pain meds (2)
- sedatives
2. morphine
wound w/ clean approximated edges. Clean dry in-tact CDI. Surgical wounds
1st intention healing
wound w/out clean edges and are not approximated. Higher chance for infection
2nd intention healing
Identify common signs and symptoms of cardiovascular conditions (5)
- peripheral cyanosis
- dyspnea
- Angina
- Edema
- Fatigue
Identify common s/s of respiratory diseases (5)
- cough
- dyspnea
- central cyanosis
- angina
- pulmonary edema
describe common PT interventions for pts w/ repiratory pathologies (4)
- airway clearance
- postural draining
- breathing ex
- endurance ex
UMN diseases (5)
- SCI
- MS
- CVA
- TBI
- Parkinsons
characteristics of UMN diseases
spasticity, clasp-knife
LMN diseases
- polio
- peripheral nerve injury
- muscular distrophy
characteristics of LMN diseases
paralysis, atrophy
chest pain caused by ischemia to myocardium
angina pectoris
hardening of arteries due to fatty cholesterol plagues
atherosclerosis
hardening of the walls of arterioles due to fatty cholesterol plagues
arteriosclerosis
sudden stopping of the heart
Myocardial infarction
high blood pressure resulting from genetics, diet, stress or lifestyle
HTN
a result of endocarditis that creates an increased workload for the heart
valve disease
chronic inflammation of the bronchial tree where productive cough is present for 3 consecutive months for 2 years or more. Blue bloater
chronic bronchitis
destruction of the walls of the alveoli caused by cigarette smoking. No cough. Pink puffer
Emphysema
hereditary disease of the pancreas. Malfunction of mucous membranes of pancreas and lungs
cystic fibrosis
acute, reversible inflammatory obstructive pulmonary condition. Caused by external stimuli. Excess mucous
asthma
inflammation of the aveoli and small bronchi caused by bacteria. Common in immobilized pts
pneumonia
bacterial lung disease transmitted through coughing or sneezing
TB
heart is not able to pump enough blood to meet the body’s needs due to L or R ventricular failure
CHF
Caused from a hemorrhage or embolus/thrombus to the brain. Stroke
CVA
autoimmune neurological disease causing greatest weakness at 3 weeks from onset of symptoms
Guillain Barre
external injury to the head causing damage to brain tissues.
TBI
Autoimmune demyelinating neuro disorder which has 2 types. Primary progressive and relapsing remitting
MS multiple sclerosis
affects basal ganglia where dopamine is not being produced properly
Parkinson’s
Any injury to the CNS caused by congenital abnormalities before, during or immediately after birth
cerebral palsy
result of trisomy on chromosome 21
down syndrome
neural tube defects in the development of the spinal column
spina bifida
spina bifida that is not visible to the eye. often no s/s
occulta
spina bifida where spinal cord is intact, minimal damage esp if defect is closed right after birth
meningocele
spina bifida where both meninges and spinal cord protrude through skin
mylomeningocele
excess cerebral spinal fluid accumulates, compressing the brain tissue and blood vessels. Cranial sutures are not closed.
hydrocephalus
rare disorder of the clotting mechanism of the blood
hemophilia
degenerative arthritis w/out inflammation
OA
OA where etiology is unknown
primary OA
OA caused from previous injury, infection, hyperthyroidism, obesity, stress
secondary OA
degenerative disease affecting the intervertebral discs. “arthritis of the spine” cervical
spondylosis
defect of the pars interarticularis of vertebrae in L5-S1 area. Less severe
spondylolysis
fracture of the pars and vertebrae slips anteriorly. Most severe. Avoid extension
spondylolisthesis
joint infected by a virus or bacteria. Most common in young, old, immunosuppressed or those who use drugs
infective arthritis
crystal like formation w/in the jt from metabolic inability to process uric acid. Big toe. Genetically x-linked
gout
bilateral, symmetrical arthritis. Inflammatory, systemic, connective tissue and autoimmune disease
RA
disease of brittle bones, more common in women and can be caused by reduction in estrogen (hormonal changes)
osteoporosis
inflammation of the bone caused by infection
osteomyelitis
heartburn caused by acidic contents which regurgitate up into the lower esophagus
GERD
chonic autoimmune disease affecting mainly the small intestine
Crohn’s
gallbladder stones
cholelithiasis
intense R lower ab pain. (McBurney’s point)
appendicitis
non-erosive gastritis
chronic gastritis
erosive gastritis
peptic ulcer disease
nonspecific intestinal condition. Does not damage intestines
IBS
glucose below 70mg, weakness, shaking, sweating, hunger
hypoglycemia
glucose above 300mg, lethargy, thirst, excessive urination
hyperglycemia
chronic autoimmune intestinal conditions. Crohn’s and ulcerative colitis
inflammatory bowel disease
affects only the rectum and colon. IBD
ulcerative colitis
small finger like projections in the wall of the intestines
polyps
pouch-like process of the intestines
diverticula
what is the primary risk factor for a pt w/ DM?
infection
DM s/s (3)
- thirst
- hunger
- pee
advice for DM pts (4)
- no tight socks
- deep shoe box
- check feet daily
- exercise on the reg
PT for DM (3)
- education
- wound care
- mobility
which muscular dystrophy is the most severe?
DMD
DMD life expectancy
late teens/early adults
BMD life expectancy
midlife
condition in which one or more arteries in the lungs becomes blocked. Central cyanosis
pulmonary embolism
arteries that supply blood to the heart become hardened and narrowed
coronary artery disease