Paget's Disease and Osteomalacia

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Last updated 5:13 PM on 3/27/26
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75 Terms

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second most common metabolic bone disease

Paget's disease

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describe the bones that form with Paget's disease

new bone formation abnormal

bones are enlarged but weak

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___ occurs in bone marrow of paget's bones

fibrosis

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Paget's pathogenesis

unknown

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Paget's demographic

over age 50

men and women

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risk factors for paget's

environment

virus

genetics

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phases of paget's

1. osteoclastic

2. osteoblastic sclerotic phase

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phase 1: osteoclastic (resorptive stage)

bone resorption occurs too quickly for osteoblasts to keep ip

causes lytic areas of bone

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phase 2: osteoblastic sclerotic phase

heavily calcified and enlarged bone made

not well organized

weak bones

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commonly affected sites of paget's

skull

spine

pelvis

femur

tibia

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paget's symptoms

asymptomatic (80%)

hypercalcemia

affected bone changes shape and size

skull involvement

tumors (osteosarcoma)

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diagnosis of paget's

x ray

bone scan

labs - alkaline phosphatase

bone biopsy

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treatment of paget's

anti-inflammatory medications

bisphosphonates

surgery for fx

no cure

exercise

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prognosis of paget's

varies

osteosarcoma occurs in 1% of pts

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compare osteoporosis and paget's disease

x

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osteomalacia

failure or deficiency of normal calcification/mineralization of bone matrix

leads to soft and weakened bones

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2 common causes of osteomalacia

1. insufficient calcium absorption

2. increased renal phosphorus loss

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risk factors of osteomalacia

inadequate diet

lack of sunlight

intestinal malabsorption

renal failure

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children can get osteomalacia because

breast fed infants of malnourished women

not vitamin D fortified milk in diet

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dietary cause of osteomalacia largely being eradicated in the US

vitamin D enriched milk

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regulates calcium absorption in body

vitamin D

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2 sources of vitamin D

diet

sun exposure

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t/f: vitamin is not active until it reaches the stomach or skin

false

not active until it is processed in the liver and kidney

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osteomalacia pathogenesis

bone matrix intact

decrease in calcification (matrix is uncalcified)

osteoid formed

bones bend/deform because they are soft

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diagnosis of osteomalacia

mimics other conditions

diffuse aching/fatigue

proximal muscle weakness

weight loss

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testing for osteomalacia

bone biopsy

blood work

urinalysis

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treatment of osteomalacia depends on

cause

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treatment for osteomalacia

Vitamin D, calcium supplementation

braces/sx

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osteomyelitis risk factors

recent sx/joint replacement

direct penetrating trauma

IV drug users

immunocompromised

medications

other infectious diseases present

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common bacteria of osteomyelitis

staphylococcus aureus

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concerns with osteomyelitis

antibiotic resistance

sx to drain joint, remove tissue

can lead to AVN and eventually joint replacement

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osteomyelitis

acute or chronic inflammation of bone secondary to an infectious organism

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exogenous osteomyelitis

direct extension into bone

from wound, trauma, sx

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hematogenous osteomyelitis

spread of organisms via blood

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acute/chronic hematogenous osteomyelitis is more common in children

acute

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acute/chronic osteomyelitis is more common in adults and immunocompromised individuals

chronic

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symptoms of osteomyelitis

erythema/edema over site

pain

fever, malaise

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diagnosis of osteomyelitis

history

cultures

imaging

biopsy

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treatment of osteomyelitis

IV antibiotics

surgery

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if osteomyelitis is untreated for more than 1 week to 10 days

permanent loss of bone structure can occur

permanent loss of bone growth (children_

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t/f: osteomyelitis is only an acute condition

false

can be acute or chronic

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#1 cause of prosthetic failure

infection

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80% of prosthetic infections are

staph

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most infections following a joint replacement occur because of:

a. wound infection or operative contamination

b. dental, skin, respiratory, UTI

a

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why is it hard to identify an infection following a joint replacement?

swelling, redness, increased temperature are signs of infection but also normal following sx

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when do prosthetic/implant infections most commonly occur?

within first year

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risk factors for prosthetic infections

prior surgery at site

RA

immunosuppression

diabetes mellitus

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t/f: even when an incision is closed, patient's joint can still become infected

true

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with a severe infection of a prosthetic, the prosthetic will be

removed

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joint replacement infection treatment

remove implant

debride tissue

antibiotic cement

IV antibiotics for at least 6 weeks

new joint replacement

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diskitis

bacterial infection of disk space between vertebrae

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t/f: diskitis does not usually occur in children

false

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in children, diskitis might occur because of

respiratory infection

UTI

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In adults, diskitis might occur because of

post-op complication

post-injection

UTI

URI

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diskitis (may/may not) be relieved by rest

may not

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red flags in children relating to diskitis

inability/refusal to flex spine

LBP*

fever*

wont WB or walk

hip extension pain

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diskitis diagnosis

x ray

MRI

cultures

bloodwork

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diskitis treatment

rest antibiotics

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diskitis prognosis

good but pain may persist

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infectious (septic) arthritis

bacterial infection in joint

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causes inflammation of synovial membrane, which destroys cartilage, and causes pain/arthritis

infectious (septic) arthritis

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reactive arthritis

acute, asceptic inflammation arising after infection but at a site remote from primary infection

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causes joint to have inflammatory response, causes pain/arthritis

reactive arthritis

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septic arthritis common causes

staph

gonorrhea

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fluid aspiration must be done with

septic arthritis

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primary risk factor for septic arthritis

pre-existing abnormal joint

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common joints for septic arthritis

hip

knee

ankle

elbow

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prognosis is good for septic arthritis if treatment is initiated during what time frame?

5-7 days

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t/f: any infection in a joint is not considered a medial emergency

false

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when can articular cartilage and subchondral bone be destroyed within?

17 days

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commonly infected bursa

olecranon bursa

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tendon can be infected by

spread of infection along synovial sheaths

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reiter syndrome demographic

male, 30, sexually active

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reiter syndrome symptoms

cant see, cant pee, cant climb a tree

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risk factors for AVN

alcoholism

decompression sickness

hip dislocation

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