Spinal + Other disease affecting Jts Flashcards
Degen Disk Disease (DDD)
peaks at ____
Epidem
Clinical Manifes + Complication
Most common cause of ____
Tx
Lumbar DDD early onsit, 5% adult peak 40-50
Genetics most impt 50-70%
Age+weight 2ndry
Sciatica: Men 1.5-3x
Dehydr nucelus pulp, fibrous stress tears annulus = disk collapse
Stenosis (narrow), spondylolisthesis (vert. shift fwd)
–
LB(P) + radiculopathy (symp re: nerve pinch in VC)
Disk fail is irreversible. Bed rest NOT standard care, surgery (diskectomy), replacmt, fusion
Rheumatoid arthritis (RA)
Affects:
Onset peaks @ ___, ____prevalent
_____ women and _____ incr. risk by ____
Etiology
Prog.
Affect CVP, GI , Eye, osteo
Nulliparus, not taking contraceptive - 4x
—
T-lymph into synov fluid
—
Irreversible, QOL mgmt - mobility, stiffness, edema, destruction. Jt defrm-sublux, Ulnar dev., asymp subcut nodul in organ
RA Diagx
RA clinical manifestations
80% +ve for RF (rheumatoid factor)
Pannus
Systemic Disease, insidious - general (P), weakness - wrist, knee, fingers
Juvenile Idiopathic Arthritis (JIA)
3 type
Prog
Arthritis starting <16y
Girls (1-5yrs) more: Oligoarthritis or pauciarticular (50% all JIA) Mild. \: knees, elbows, wrist, ankle) Polyarticular (40% of all JIA), 5+ joints. More severe.
Equal sex: (Still’s disease) Systemic-onset. Severe.
Mortality 3-5x, No cure, immuno-modulatory, preserve ROM, dec. (P)
Ankylosing spondylitis
Epid, onset at _____y
Clinical Manifest
Prog
Marie-Strumpell: Inflammatory of axial sk w/ asym involv (hip, knee, shoulder)
Higher in Caucasian, onset at 15-30y, rarely 40
Men 2-3x, 90% faulty gene = 2% dev
- Insidious onset, (low back, buttock, hip pain for >3mths)
- (P) not below knee, loss of Lumbar lord, incr. thor Kyp.
Fusion IV Disk space (bamboo x-ray)
Mgmt (maintain mobil, red. inflam, prev frax)
Sjorgen Syndrome
Epid ___ most comn ____
Clinical Manifest
Mgmt
Autimmune arthrits-re: affects - Moisture-producing gland Mouth + eyes. Lung, kidney, Liver
2nd most cmn autoimmue rheumatic, high malignancy risk
Dry throat (detnal decay), esophag, gastr,
Moisturize dryness/eye infec
Psoriatic Arthritis
Etiology
Clinical Man
Affects 20% of severe psoriatic pt
Genetic, 80-90% dev if 1st degree relative with disorder
Distal IP finger jt (Claw), no cure usually mild
Lyme Disease
Bacterial disseminates ___ and survives for ___
Clinical Manifest early dissem
Diagnosis + Tx
Chronic arthritis from untx Lyme in NA most cmn, most cmn vector-borne infectius disease in US
Usually unilat
blood stream/lymph, years
–
Fatigue, chills, skin erythema, fever
Bloodtest Spriochete antibodies (late stages of infect - 32 days), Antibiotic Tx.
No natural immu from B. Brugdorferi
Gout ____ disorder marked by ____ + ____ in___
3 group
Incidence/Epid
Clinical Manifestations
Metabolic disorder by elevated Uric acid in jts, soft tissue and kidney
Primary hyperuricemia (inherit)- Middle age, peak 50, symptomatic post 10-20 yr of hyperuricem, women post-meno
2ndry (Rduced kidneyf - leukemia, psoriasis, chemo) block xcrtion of urin acid)
idiopathic
Acute monoarticular inflam arthritis, @ night of 1st MTP jt
Gout Clinical manifest mechanism
Tophus (deposit of uric crystals, leukocytes splat = inflam)and bone abnormalities
Pseudogout
Epid
Calc crystal deposit not urate, knee of older women
Reactive Arthritis
Presentation, prog
Post-artic. infect remote from primary
> 1 jt affect, usually not SI, good prog
Reiter’s Syndrome
Symptoms
Tx
cmn reactive arthritides, follows Ven. Disease (Clamydia), or enteric infec (shigella, salmonella
Triad: Urethritis, conjunctivitis, arthritis
Antibiotic Tx may not help, resolves in 3-12mth, may recur.