Maternal Flashcards

GI, MUSCULO (62 cards)

1
Q

Assessment of musculoskeletal

A

Bone radiography
Bone scan (scintigraphy)
Electromyography
Bone Biopsy
Muscle Biopsy
Arthroscopy
Magnetic resonance imaging

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2
Q

-Specialized radiology
-Identify areas physical and chemical changes
-Follow progress of treatment

A

Bone Scan (scintigraphy)

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3
Q

-Measure muscle response/ electrical activity-> nerve’s
-one or small needles(electrodes) inserted through the skin

A

Electromyography

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4
Q

-removal of small piece of of muscle tissue for examination
-removal of a plug of tissue by needle, used for examination
-sometimes more than one is needed to obtain large specimen

A

Muscle biopsy

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5
Q

-small bone sample removed from outer layer of bones opposite to bone marrow in which the innermost layer part of bone
-sample retains architecture of bine when seen histopathological examination slide

A

Bone biopsy

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6
Q

Surgical procedure of orthopedic surgeon
-visualize and treat problems inside a joint
-diagnose and treat joint problems
-inserts a narrow tube attached to a fiber optic video camera through a small incision (buttonhole)
-view transmitted to a high definition video monitor

A

Arthroscopy

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7
Q

-examine bones, joints & soft tissues
-cartilage muscles, tendons
-injuries, structural abnormalities inflammatory disease, congenital abnormalities, osteoporosis ocslerosis, bone marrow disease and herniation

A

Magnetic Resonance Imaging

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8
Q

-pigeon toe
-result of foot, tibial, femoral or hip displacement
-feet point inward while walking

A

Toeing-in

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9
Q

-relaxation of longitudinal arch of foot
Factors:
-obesity
- injury to foot or ankle
-rheumatoid arthritis
Aging
-diabetes

A

Flat feet (pes planus)

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10
Q

-opposite of genu varum
- medial knees touch and medial aurface of ankle melleoli are separated more than 3 inches

Causes
-increased vascularity occurs during fracture healing resulting in medial metaphyseal overgrowth
-radiation,infection and tumors. ( osteochondromas ,multiple hereditary esotoses,fibrous dysplasia

A

Knock knees (genu valgum)

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11
Q

-lateral bowing of tibia
-most common cause is rickets or condition that prevents bones from forming properly
-infection, tumors can affect growth of the leg which can cause one eg to be bowed

A

Bow legs ( genu varum)

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12
Q

-Genetic or heritable
-bones fracture easily no obvious cause or minimal injury
- brittle bone disease
-can be severe or mild
-defects r/t protein (1 collagen) building block of body
-type 1 collagen make bones strong and build tendons, ligaments , teeth and sclera
-mutation or gene changes causes collagen defects

A

Osteogenesis imperfecta

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13
Q

-infection of the bone
-Mostly caused by bacteria
-may be cause by fungi or other germs
-may spread to bone from infected skin, muscles, or tendons next to the bone

A

Osteomyelitis

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14
Q

Osteomyelitis in younger children caused by

A

Streptococcus pyogenes

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15
Q

Osteomyelitis in older children caused by

A

Staphylococcus aureus

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16
Q

Limitation of weight bearing on affected part
-bed rest and Immobilization
-administration of oxacillin (Bactocill) hospital and then home for 2weeks, oral 3-4 more weeks
-administration of biphosphonates- reduce bone loss

-aspirate bones tube inserted to the area for antibiotic solution
- drainage tubes attach to suction to evacuate subperiostrum area

A

Osteomyelitis

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17
Q

-inflammation in hip joint
-causes pain, limp, and sometimes, refusal to bear weight
-occurs in pre-pubescent children most common hip joint
-occurs when viral infection upper respi infection moves to and settles in hip joint
-in Healthy person (cause) overuse or stress movement of joints- inflammatory arthritis

A

Transient synovitis

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18
Q

-Overuse injury occurs after repetitive activities of the muscles attached to ____
-excessively tight hip and thigh muscles prone to pelvis/hip ______
- traction injury o cartilag and bony attachment of tendons in children and adolescents
-overuse injury in children who are growing have rights or inflexible muscle tendon units

A

Apophysitis

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19
Q

Types of scoliosis

A

-Functional (postural ) scoliosis
-Structural scoliosis

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20
Q

Lateral curvature of spine
Compensatory mechanism of unequal leg length
- curvature is flexible will go away if problem side goes away

A

Functional ( postural) scoliosis

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21
Q

Is idiopathic, permanent curvature
-damage to vertebrae
-spine curvature not flexible
-does not go away

A

Structural scoliosis

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22
Q

-if curve is less than 20 degrees no therapy is required until 18 years
-long term treatment
-mechanical bracing to maintain spinal stability and prevent further progression until bone growth is complete
-rehabilitation

A

Structural scoliosis

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23
Q

-involves joints of body also affects blood vessels and connective tissues
-symptoms must begin before age 16 years old and last longer than 3 months

A

Juvenile Arthritis

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24
Q

-heat application
-warm water soaks 20–30 minutes
-paraffin soaks
-splinting to immobilize
-

A

Therapy for juvenile arthritis

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25
-not common for a child to sustain a finger injury from a slammed car door -causes crushing blow to the tip of the finger- excruciatingly painful
Finger injuries
26
results in crushing, lacerating injury that quickly becomes edematous.
Bicycle-spoke injuries
27
muscle-tendon injury
Strain
28
is a ligament injury
Sprain
29
-chronic neuromuscular disease -causes weakness in the skeletal muscles(muscle that connect to your bones and contract to allow body movement in the arms and legs, and allow for breathing) Face and throat muscles(Impair speaking; Cause difficulty swallowing; Affect chewing; Change facial weakness in your neck, arms and legs. difficulties with speech, chewing, swallowing and breathing. expressions weakness and rapid fatigue of any of the muscles symptoms: Eye muscles ptosis drooping of both eyelids, double vision
Myasthenia gravis
30
Administration of Neostigmine (Prostigmin) OR Pyridostigmine bromide (Mestinon)
Myasthenia gravis
31
Does not look ill Head maintained in a flexed attitude; unable to extend Mental status and cognition: normal speech: dysarthric L/eye: partial ptosis Pupils: B/L equal and reactive Cranial Nerves: CN 3,4,6: ocular movements normal CN 9,10: soft palate does not move Other CN: normal Upper and lower limbs: normal in inspection, tone, power and reflexes Sensation: no deficits Cerebellar function: retained Gait: no abnormality detected Fatigability: present on repetitive closure of eyes
Myasthenia gravis
32
- of a group of rare diseases called the inflammatory myopathies -chronic (long-standing) muscle inflammation, muscle weakness, and in some cases, muscle pain. -occurs from the degeneration of skeletal muscle fibers. -unknown. may be due to a viral infection of the muscles or a problem with the body's immune system. -occur -people who have cancer in the abdomen, lung, or other parts of the body or and autoimmune basis suspected.
dermatomyositis
33
general term used to describe a number of conditions affecting the muscles
Myopathy
34
can appear suddenly or develop gradually over time. The most common signs and symptoms include: Skin changes..
DERMATOMYOSITIS
35
-violet-colored or dusky red rash develops, most commonly on your face and eyelids and on your knuckles, elbows, knees, chest and back. The rash, which can be itchy and painful, is often the first sign of dermatomyositis.
Skin changes.
36
Progressive muscle weakness involves the muscles closest to the trunk, such as those in your hips, thighs, shoulders, upper arms and neck. The weakness affects both the left and right sides of your body, and tends to gradually worsen.
Muscle weakness.
37
confirm a diagnosi of dermatomyositis, a doctors may perform
Skin and Muscle Biopsies punch biopsy, in which a dermatologist uses a device that resembles a pencil to puncture the skin and remove a small tissue sample
38
Treatment for dermatomyositis
High dose of corticosteroids, Methotrexate, or specific immunosuppressant
39
group of muscle diseases caused by mutations in a person's genes. -muscle weakness decreases mobility, making everyday tasks difficult. -cause progressive weakness and loss of muscle mass.
MUSCULAR DYSTROPHIES
40
MUSCULAR DYSTROPHIES
Congenital Facioscapulohumeral Pseudohypertrophic (Duchenne Disease)-
40
affects boys and girls and is apparent at birth or before age 2. -Some forms progress slowly and cause only mild disability, while others progress rapidly and cause severe impairment.
Congenital
41
-weakness typically begins in the face, hip and shoulders. shoulder blades might stick out -occurs in the teenage years but can begin in childhood or as late as age 50.
Facioscapulohumeral
42
most common form of muscular dystrophy -inherited as a sex-linked recessive trait. -occurs only in males; females may carry the gene may demonstrate some symptoms and usually apparent by 3 years of age.
Pseudohypertrophic (Duchenne Disease)-
43
remain ambulatory for as long as possible Therapeutic Management: *range-of-motion exercises. * Splinting and bracing may overweight, remaining ambulatory becomes even more difficult for them. * Encourage a low-calorie, high-protein diet to avoid excessive weight gain. In addition, to prevent constipation because of poor abdominal muscle tone, encourage a high intake of fiber and fluids. * A stool softener may be necessary. In the meantime. corticosteroid therapy is helpful to increase function and strength at least on a short-term basis; help parents understand the importance of this and have a set schedule of administration. Newer therapies include cell repair, gene transfer, and stem cell (Sun et al., 2020). *
Muscular dystrophies
43
The average life expectancy of these Muscular dystrophies patients has improved and currently is about
35 to 40 years.
44
-break in the continuity or structure of bone. -Bone in childhood is fairly porous, allowing bones to bend rather than break. periosteum is thick, so the bone may not break all the way through. * Epiphyseal lines may cushion a blow so that the bone does not break. * Healing is rapid as a result of overall increased bone growth.
Fracture
45
children with a suspected fracture need an X-ray, firm the diagnosis and to determine the alignment a position the amount of end-to-end contact there is bone fragments). bayonet or side-to-side apposition may be established for children up to 10 or 12 years old.
Therapy to fracture
46
treat a wide range of musculoskeletal disorders, from simple fractures in the extremities to correction of congenital structural bone disorders.
Cast
47
Casts are created from either
Plaster of Paris or Fiberglass.
48
children's casts because it is light in weight; comes in attractive colors; and, when a special waterproof liner is used, can be immersed in water. * Unfortunately, it is more expensive and may not be practical for casts that need frequent changing,
Fiberglass
49
plaster cast takes _____hours to dry depending on its size.
10 to 72
50
Fiberglass casts usually dry within _____minutes.
5 to 30
51
used to protect the foot and ankle after an injury or surgery.
Medical Walking Boots
52
type of walking aid that serve to increase the size of an individual's base of support.
Crutches
53
practice of slowly and gently pulling on a fractured or dislocated body part. It's often done using ropes, pulleys, and weights.
Traction
54
to guide the body part back into place and hold it steady.
Traction
54
These tools help apply force to the tissues surrounding the damaged area.
Ropes, pulleys and weights
54
Types of Traction
Skeletal and skin traction external fixation OPEN REDUCTION AND INTERNAL FIXATION And HALO TRACTION
55
far less invasive than skeletal traction. It involves applying splints, bandages, or adhesive tapes to the skin directly below the fracture. The affected body part is then pulled
Skin traction
55
placing a pin, wire, or screw in the fractured bone. After one of these devices has been inserted, weights
Skeletal traction
56
can be adjusted externally to ensure the bones remain in an optimal position during the healing process.
External fixatin
57
pull the head and spine upward carefully, applying a slow stretch to the spine. Doctors do this by attaching a halo