Alternation In Mobility / Neuromuscular, Muscoskeletalk & Pressure Ulcer Handout Flashcards

1
Q

> 50% of pressure ulcers in neonates/kids are due too..

A

Equipment pressure injury

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2
Q

Hihh risk conditions for pressure ulcers in peds…

A

Spinal Bifida/ Cerebral palsey

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3
Q

How often skin assessment in peds

A

Daily

Medicare will not reimbursement stage III or IV unless present upon arrival

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4
Q

Site most likely fir pressure ulcer

Small child

Older child

A

Small = Occiput

Older = Sacral

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5
Q

Brain & spinal cord myelination is incomplete at birth describe how process of myelination…

A

Cephalocaudal - Head - toe and
Inwards outward

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6
Q

Hypertrophy…

A

Muscle growth

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7
Q

Epiphyseal plates…

A

Growth plates in long bones.

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8
Q

Cast are applied after swelling has decreased to avoid…

A

Compartment syndrome

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9
Q

Cast will require Stockinette/ padding to avoid injury.

Removed with…

A

Cast saw

Vibrates but cannot cut skin

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10
Q

Do this if skin under cast is itchy…

A

Cool hair dryer setting

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11
Q

When to elevate extremity in a cast…

A

First 1 or 2

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12
Q

Teach SS of compartment syndrome…

A

5 Ps

Pain
Pallor
Pulselessness
Paresthesia
Paralysis

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13
Q

Therapeutic tech to apply a pulling force to a part of the body (Bones, Joints, Muscles)

A

Traction

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14
Q

Traction

Therapeutic tech to apply a pulling force to a part of the body (Bones, Joints, Muscles)

Goal….

A

Alignment broken bones / dislocated joints

Reduce muscle spamsm

Correct deformities

Relief of pressure on nerves

Immobilize limb before or after surgery

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15
Q

Neurovascular checks for 5 Ps how often for pt in traction…

A

1-2 initially

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16
Q

Traction Setup.

Ensure the weights rest on the floor at all times.

T ir F

A

F

They must hang freely

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17
Q

Complications frequent with traction…(4)

A

Constipation
DVT
Urine retention
Pressure ulcers

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18
Q

External fixation purpse…

A

Pins & screws inserted into bone and connected to wire frame outside the body to stablize bone while it heals

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19
Q

Benefits of external fixation ….

A

Stabilize complex / open fractures

Allows soft tissue healing- burns, wounds, infections

Temp stability b4 surgery

Correct bone deformities

Maintain alignment after surgery

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20
Q

Pin site cleaning for external fixation…

Type of technique…

Type of cleaner….

A

Sterlie tech

Chlorhexidine

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21
Q

Muscoskeletal assessment.

Inspection…

Palpation…

ROM…

Strength Test…

A

Inspection; Swelling, bruising, redness, asymmetrical / Muscle Wasting

Palpation: tenderness, warmth, crepitus, masses

ROM: Active & passive

Strength; Push / Pull 1 - 5

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22
Q

Neurovascular assessment consists of circulation, sensation, motion.

Critical after injury, surgery, casting

Describe assessment…

A

6 P’s

Pain
Pallor
Pulselessness
Paresthesia
Paralysis
Pressure

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23
Q

Spina bifida occulta occurs when the vertebrae fail to completely close around the spinal cord.

Nerves usually Uneffected

What does it look like…

A

Dimple on lower back

Small tuft of hair

Birthmark

Lipoma (small fatty lump)

Dermal pit

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24
Q

Clinical Significance of spina bifida occulta…

A

Mostly asymptomatic

Rarely Tethered Cord Syndrome- spinal cord is abnormally stretched

Back pain
Leg weakness
Bowle / bladder
Change in Gait

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25
Meningocele....
Moderate form of spina bifida Meninges protrude through vertebrate DONT CONTAIN SPINAL CORD TISSUE
26
CSF- filled sac visible on back near lumbar or sacral area. Spinal cord remains in place & neurological function is preserved Sac breaks = Medical Emergency
Meningocele
27
Meningocele is a CSF filled sac located on the lower back Neurological function often intact Pre op care: Protect the sac Dressing... Posistion... Diapers.... Monitor for this serious problem...
Saline soaked non-adherent bandage Prone posistion Diaper under the sac Monitor for meningitis
28
Myelomeningocele....
Most severe spina bifida Meninges & spinal cord / nerves protrude through opening in vertebrea
29
Myelomeningocele Neurological defects below level of lesion Physical findings Visible sac at birth Lower limbs... Bowles/bladder.... Clubfoot, dislocated hips, ortho deformities Hydrocephalus....
Lower limbs = Flaccid paralysis Incontinence Hydrocephalus 80 -90%
30
Posistion for myelomeningocele Posistion... Head... Diapers... SAC Care Type of allergy common among this population...
Posistion: Prone / hips slightly flexed, legs abducted with pad Head turned to 1 side Dint use diapers SAC Care Saline soaked bandage Latex allergy
31
Labs & Screening for myelomeningocele Maternal AFP... Amniocentesis...
Parental screening for neural tube defects Amniocentesis can detect levels of AFP
32
Spina bifida occulta Meningocele Myelomeningocele External appearance & problems involved with disorder...
Spina bifida occulta Red, dimples, tuft of hair - incomplete close of vertebrae- Back / leg pain Meningocele: Visible CSF filled sac & Meninges Neurological issues rare. Myelomeningocele Large CSF, Meninges, nerves in a sac on lower back. Hydrocephalus common Parálisis, sensory loss, bowel / bladder dysfunction
33
Talipes Equinovarus (Club Foot) is a defect in which one or both feet are twisted out of posistion. Define Cavus... Adduction... Varus... Equinus...
Cavus High Arch Adduction Forefoot turns inwards Varus heel turns inwards Equinus Tip Toe posistion
34
Gold standard for treating Club Foot...
Ponseti Method Serial casting started soon after birth Gentle manipulation of foot followed by long leg casting Chnge casting weekly for 6 - 8 weeks
35
Osteogenesis imperfecta....
Brittle bone disease Break easily due to defect in tyoe 1 collagen Inherited Autosomal Dominate (most common) or Autosomal Recessive Type 1 Mild Tyoe 2 lethal at birth
36
Osteogenisis imperfecta Blue sclerae... Hearing loss... Short statue Joint laxity Spinal curvature... Family history
Collagen in eyes give a blue tint Hearing loss due to abnormal ossicles Kyphosis / Scoliosis
37
Medications for osteogenisis imperfecta...
Bisphosphonates (pamidronate) Improves bone density
38
Femoral head and acetabulum are misaligned or unstable...
Dev Dysplasia of the Hip
39
Risk of development Dysplasia of the hip. Birth order... Male / Female... Birth posistion... Family history... Oligohydramnios.... Swaddling tight...
First born risk - less uterine space Female x 5 odds due to maternal hormone Breech posistion Genetic predisposición Low amniotic fluid can restrict movement Swaddling with hips extended & adducted
40
Development Dysplasia of the hip Clunk heard as femoral head is reduced into acetabulum. Hip dislocation when adduct3d and pushed posteriorly Barlow sign Ortolani sign
Clunk heard as femoral head is reduced into acetabulum - Ortolani sign Hip dislocation when adduct3d and pushed posteriorly - Barlow sign
41
Infants: Positive Ortolani/ Barlow signs Asymmetrical gluteal / thigh folds Limited hip abduction Leg length discrepancy Older Chillin Limping/ Tip toe walker Trendelburg sign: Pelvis dips on unaffected side when standing on affected leg Hip pain (less common)
Hip Dysplasia
42
Treatment for Development Hip Dysplasia New born - 6 months.... 6 - 18 months.... >18 months...
New born - 6 months: Pavlik harness: Keeps hips flexed and ABDUCTED (23 - 24 Hrs Daily) 6 - 18 months: closed reduction/ Spica cast >18 months: Open Surgical reduction, possible osteoporosis, casting
43
Pavlik Harness Considerations When to adjust straps... Wher3 to wear harness in relation to diaper...
Adjust only with providers blessing Wear over diaper, undershirt, under straps to protect skin
44
Muscle fibers are gradually replaced by fat & connective tissue in this progressive genetic disorder that leads to muscle weakness/ degeneration....
Muscular dystrophy (group of genetic disorders)
45
The most common & severe progressive/ genetic disorder that replaces muscle tissue with fat / connective tissue...
Duchenne Muscular Dystrophy
46
MD is an X linked recessive disorder. Which population is most affected by this disease...
Boys Girls are carriers
47
When do symptoms appear for MD...
2 - 5 yrs
48
Gowers sign...
MD Chold uses hands to Walk Up thighs to stand from floor
49
MD Progressive muscle degeneration Begins in this area.... Describe gait... Enlargement of... Loss of ambulation by age... Can lead to heart / ling failure Some cases Mild Cognitive Delay
Begins in Pelvis & Shoulder Gridles & move up Waddling Gait Enlargement of Calves Loss of ambulation by age 10 - 12
50
MD - Respiratory support Teach use of... Eventually use of...
Cough assist device Bipap
51
Medications for MD (3)
Corticosteroids ACE Inhibitors/ beta-blockers
52
Non-progressive disorder of muscle, movements, muscle tone, posture caused by Damage to Develpong Brain - before or during birth...
Cerebral Palsey
53
Cerebral Palsy is a non-progressive disorder that affects movement, muscle tone, or posture and is caused by damage to developing brain. Timing (Pre, Peri, Post - Natal) Birth Asphyxia, premature , low birth weight, birth trauma TBI, Meningitis, encephalitis, stroke, kernicterus Brain malformation, Intrauterine infection (CMV, Rubella), maternal drug used, placenta insufficiency
Perinatal Birth Asphyxia, premature , low birth weight, birth trauma Postnatal TBI, Meningitis, encephalitis, stroke, kernicterus Pernatal Brain malformation, Intrauterine infection (CMV, Rubella), maternal drug used, placenta insufficiency
54
Duchene MD Spastic (Most Common) Dyskinetic/ Athetoid Ataxic Mixed
Spastic (Most Common) Stiff muscles, jerky, tight joints, can affect just 1 limb / side or everything Dyskinetic/ Athetoid Involuntary movements esp in face and tongue / drooling & speech issue Ataxic Poor balance, unsteady gait, difficulty with depth perception/ coordination Mixed Combined disorders esp Spastic & athetoid
55
Medications for MD For spasiticy... Targeted muscle relief... Seizures....
For spasiticy: Baclofen / Diazepam Targeted muscle relief: Botox Seizures: Anticonvulsants
56
Slipped Capital Femoral Epiphysis....
Head of femur slips off growth plate (epiphysis) at the hip joint. Like a scoop of ice cream slipping off a cone MEDICAL EMERGENCY- Risk of Avascular Necrosis
57
Describe population most at risk....
10 - 16 yrs Boys Fat Black / latino Endocrine disorder, trauma, fam history
58
Treatment Slipped Capital Femoral Epiphysis Immediate.... Surgery... Bilateral fixation maybe considered if hips are at high risk
Crutches / wheel chair until surgery In-situ pinning (metal screw holds head of femur in place)
59
Lateral side to side curvature of the spine >10 ° often with vertebral rotation...
Scoliosis
60
This disease can be Structrual (Permanent) or non-Structrual (Temp. Due to posture) Usually becomes noticeable during growth periods...
Scoliosis
61
Scoliosis 3 variations Idiopathic Congenital Neuromuscular abnormal spinal formation in utero Relat3d to Neuromuscular diseases (CP / MD) Unknown cause, more common in girls
Idiopathic: Unknown cause, more common in girls Congenital: abnormal spinal formation in utero Neuromuscular: Relat3d to Neuromuscular diseases (CP / MD)
62
Non surgical Therapeutic Management <25° 25 - 45°
<25° Observation & regular X-rays monitor 25 - 45° Bracing (Boston Brace) stops progression. Worn 16 - 23 hrs daily.
63
Surgical management of scoliosis Spinal fusion with rods & screws ____ ° of spinal curvature needed.
45 - 50
64
Post op for scoliosis surgery Log rolling for how long... No bending, twisting, lifting >10lbs.... No gym / pe... Avoid prolonged sitting...
Log roll 2 days post op Bending, twisting, lifting, >10lbs 6 - 12 weeks up to 6 months Gym/ PE 6 months Sitting first few weeks
65
Pain management post scoliosis surgery... Neurovascular checks lower extremities Respiratory... Eliminating... Psychosocial support
PCA / IV opiods Incentives spirometry / assess lung sounds Constipation/ give stool softeners
66
5 types of growth plate fractures Straight Above Lower Through Rammed Worst prognosis Often leads to growth arrest Through growth plate & metaphysis. Most common type Good prognosis Through growth plate & epiphysis. Can affect joint & mod risk to growth Across the growth plate. Good prognosis Through metaphysis, physis, epiphysis. Can lead to growth disturbances. Requires surgery
Straight Across the growth plate. Good prognosis Above Through growth plate & metaphysis. Most common type Good prognosis Lower Through growth plate & epiphysis. Can affect joint & mod risk to growth Through Through metaphysis, physis, epiphysis. Can lead to growth disturbances. Requires surgery Rammed Worst prognosis Often leads to growth arrest
67
List 5 types of growth plate fractures in order from least to most serious...
Straight 1 Above 2 Lower 3 Through 4 Rammed 5
68
Types of fractures Simple (closed) Compound (open) Comminuted Greenstick Bone breaks but skin not broken. Cast / splint treatment Bone breaks into 3 more pieces. Surgical intervention to realign Bone. Bone bends and cracks but doesn't break completely. Common in children due to more flexible bones Bone breaks & pierces skin. Requires surgery & antibiotics
Simple (closed) Bone breaks but skin not broken. Cast / splint treatment Compound (open) Bone breaks & pierces skin. Requires surgery & antibiotics Comminuted Bone breaks into 3 more pieces. Surgical intervention to realign Bone. Greenstick Bone bends and cracks but doesn't break completely. Common in children due to more flexible bones
69
Suspicious fractures.... (7)
Not yet walking Multiple with various stage of healing Ribs / sternum Both arms / legs Spiral fractures Skull / femur Lying ass parents
70
Complication of fractures Fat embolism SS
Respiratory distress Confusion Requires supportive care
71
Complications of fractures Osteomyelitis...
Bone infection- often after an open fracture
72
Juvenile idiopathic arthritis Autoimmune disorder where immune system attacks body's joints. <16 yrs Chronic pain lasting >____ weeks Morning Stiffness, may improve throughout the day. Labs: ESR & CRP... Positive ANA... Rheumatoid factor (RF)...
>6 weeks Labs: ESR & CRP Both elevated Positive ANA sometimes RF negative
73
Type of juvenile idiopathic arthritis Oligoarticular JIA (Def, Joints, Prognosis, Management) Polyarticular JIA (Def, Joints, Prognosis, Management) Systemic JIA (Def, Symptoms, Joints, Prognosis, Management)
Oligoarticular JIA Def <4 JOINTS Joints: Knee, ankel, wrist Prognosis Good but can lead to eye problems Management: Disease-modifying antirheumatic drugs (DMARDs) & biologics for eye protection Polyarticular Def: >5 typically symmetrical Joints: Hands, Wrist, Knee, Feet Prognosis: more likely Joint Damage & long-term disability Management: DMARD, Biologics, NSAIDS Systemic JIA DEF: Affects multiple systems & Joints Symptoms: Fever (evening), Rash (salmon colored/ sporadic), Enlarged Lymph nodes/ spleen, inflammation Heart, Lungs, liver Prognosis: Severe & potential life threatening Management: High doses corticosteroids & biologics
74
Methotrexate...
First line DMARD for Polyarticular/ Systemic JIA
75
Management of Juvenile Idiopathic Arthritis (6)
Meds: NSAID, DMARD,Biologics, Corticosteroids, methotrexate PT: Exercise/ ROM Orthotic Support: Splints & Braces Eye care: eye exams esp Oligoarticular JIA- due to risk of uveitis (eye wall) Surgery Psychosocial
76
In infants the spine is very mobile which can increase odds of injury...
True
77
Lordosis, kyphosis, scoliosis Describe...
Lordosis: inwards curve of lower spine Kyphosis: Hunch back Scoliosis: James Schmolen : Curvature of spine atleast 10°
78
Damage to the epiphysis may have this effect on the child....
Decreased growth
79
Difference between X ray Fluoroscopy Myelography
X ray: Must hold still Fluoroscopy: Creates photos during movement Myelography: Visualize neurotube defects
80
Gold standard for diagnosis of neuro
81
Gold standard to detect neural tube defects...
MRI/CT Can look at both hard & soft surfaces
82
Which lab result most accurately reflects muscle damage...
CK
83
Type of diet for immobilized pts...
High calorie/ high protein
84
Examples of skin traction devices...
Ace wrap Kinesiology tape
85
Straight/ Running traction Balanced suspension traction Provide counter balance to Force of traction, Can change posistion slightly, extremity is ELEVATED Force of weight pull extremities in 1 direction. Allows for extremity to rest on bed
Straight/ Running traction Force of weight pull extremities in 1 direction. Allows for extremity to rest on bed Balanced suspension traction Provide counter balance to Force of traction, Can change posistion slightly, extremity is ELEVATED
86
Russell traction...
Skin traction to put joint back in place
87
Myelomeningocele is often detectable by US during these weeks of preggers...
16 - 18 wks
88
Describe club foot appearance...
Inwards & upwards Golf club
89
Serial casting called the Ponseti method can last up to 12 weeks and is ised to help...
Club foot
90
How long after receiving the Ponseti serial casting method will a child need to wear Ankle, Foot, Orthopedic boots...
Several years possible
91
Osteogenisis imperfecta causes Porous bones, hypermobile joints, and connective tissue issues. How does one get brittle bine disease...
Autosomal Dominate defects of the collagen type 1 gene
92
Bisphosphonates are given to Osteogenisis imperfecta to strengthen bines Give 2 nursing care interventions...
Scoop instead of lift Don't lift legs to change diapers AVOID BP CUFF
93
Subluxation...
Partial dislocation
94
Maternal hormones may lead to laxity of ligaments (very flexible) in females causing this problem...
Hip Dysplasia
95
Unequal folds of skin Unequal knee height Limited abduction Trendelburg sign Problem....
Developmental Hip Dysplasia
96
Genetic mutation causes decreased/absent muscle protein dystrophin...
MD
97
Muscle Wasting/ Pseudohypertrophy Waddling Gait Lordosis (Saddle Back) Growers sign Associated with...
MD
98
Medications for MD... A (X linked recessive) affects boys progressive illness
Corticosteroids Ca & D vitamin Antidepressants Ace & beta blockers
99
Mechanically assisted cough machine maybe used with...
MD
100
CP has 2 neurological comorbidities...
Seizures & hydrocephalus
101
Class: Muscle relaxant; GABA agonist Use: Treats spasticity (especially in cerebral palsy, spinal cord injury, multiple sclerosis) Can be oral or intrathecal (pump)
Baclofen
102
Baclofen pump has an intrathecal delivery Explain medication... Explain intrathecal...
Baclofen Muscle Relaxant used in CP Intrathecal = in CSF in spine
103
Selective Dorsal Rhizotomy....
A neurosurgical procedure used to reduce spasticity (muscle tightness) in children, commonly with cerebral palsy (especially spastic diplegia). Involves cutting selected sensory nerve rootlets in the spinal cord that are sending abnormal signals to the muscles
104
Botulin Toxins Anticholinergic Baclofen, danteolene, diazepam Prescribed for...
CP
105
Slipped Capital Femoral Epiphysis Passive ROM can help...
False. It will mess them up
106
Legg-Calve-Perches Disease Avascular necrosis of femoral head Painless Common in boys 4 - 8 yrs Treatment.... Exercise.... Surgery...
Treatment: NSAIDS Limit activity Exercise: Low Impact Surgery: Not often unless >8yrs
107
What is a TLSO Brace?
Used for Scoliosis A rigid back brace that supports the thoracic, lumbar, and sacral spine. Commonly used to immobilize the spine after surgery, injury, or to treat spinal deformities.
108
Scoliosis >45° may require...
Spinal fusion
109
Scoliosis surgery is 5 - 8 hrs long How does the HCP lengthen the rods...
Magnetic Expansion Control Rod
110
Post op Scoliosis care RN helps pt to ambulate with in first 24hrs...
False PT helps with the first ambulation
111
Spiral fractures are common injuries in children...
False They are associated with abuse
112
Salter-Harris classification...
Used to classify fractures in Growth Plate
113
Juvenile Idiopathic arthritis Autoimmune disorder Antibodies attack joints Inflammation, warmth, Stiffness with activity...
False With Inactivity
114
Methotrexate is...
Antirheumatic drugs used for Juvenile Idiopathic arthritis
115
Fever Rash Enlargement of spleen / lymph nodes Anemia Fatigue Problem....
JIA
116