SCI
TBI
Mixed
Sickle Cell/ Hemophillia
JIA/Guillan Barre
100
What type of breathing pattern is due to paralyzed intercostals and/or abdominals. Describe it

Paradoxical breathing - Upper chest collapses during inspiration and belly rises excessively

100

Patient presents with crescent shaped area of blood clot on Brain CT scan. Whats the possible diagnosis ?

Subdural hematoma 

100

What is autonomic storming

increased BP, fever, Tachycardia (>130), RR >40, pupillary dilation, diaphoresis, and extension posturing. Common with TBI 

100

What are the emergencies/crisis that could occur due to sickle cell and why

Acute Chest Syndrome - Chest pain fever cough respiratory distress

Splenic Sequestration - sickle Blood cells stuck in spleen. LUQ, Tachy and Hypotension (LEFT SHOUDLER?)

Priapism - obstruction of blood flow in erectile tissue. 

Aplastic crisis - Bone marrow stops producing blood cells --> anemia

100
What are the subtypes of oligoarthritis (<4 joints)

+ANA, -ANA, HLA B27 

Oligoarthritis impacts <5 joints, muscle atrophy, must rule out infection, cancer, lyme

200
What are the stages of pressure ulcers?

1 - Non-Blanchable erythema of intact skin

2 - Partial thickness skin loss involving epidermis and or dermis. Ulcer is superficial and presents like na abrasion, blister or shallow crater

3 - Full thickness skin loss involving damage or necrosis of subcutaneous tissue 

4 - Full thickness loss with destruction of muscle bone or supporting structures 

200

What impacts treatment more than ICP, what is its normal level.

CPP 70-90. <70 stop treatment 

200
How do you differentiate between Leukemia and Lymphoma on the exam

Leukemia will presents with: Anemia, Thrombocytopenia, increased WBC, Pallor, Bleedining, Petechiae, Hepatomegaly, Splenomegaly

Lymphoma will only talk about involving different lymphoma tissue cells (Sternberg from lymphocytes T&B etc)

200

Why do many people with hemophillia need joint replacements 

Becuase they have excessive blood in the area leading to destruction of cartilage, loss of joint space, bony overgrowth, and subchondral osteolysis.  

200
Why do growth disturbances or abnomalities occur with JIA

Becuase the inflammatory response triggers pannus formation which is destructive in nature leading to epiphyseal damage and premature epiphyseal closure (sometimes asymmetrical)

300

What levels assists with cough?

Abdominals T6-L1 

Intercostals T1-11 

Quadratus lumborum - T12-L4

Serratus Posterior inferior T9-T12 

(LOT OF THORACIC T1 on)

300

What is considered a mild, moderate, or severe TBI on the Glasgow coma scale

Mild - 13-15 

Moderate - 9-12

Severe - 3-8

300

What disorder leads to small areas of hyperaeration and atelactasis next to each other in the lung leadign to a honey comb pattern on Xray. How do we treat as PT. 

CF - Airway clearance techniques, Bronchodilaters before then antibiotics, teaching coughing and huffing,postural drainage, percussion, breathing exercises, cardiovascular training, postural awareness, UE and trunk strength

300

What is the treatment for Sickle cell crisis

Pain management, Hydration, O2 therapy, blood transfusion. 

PT: Heat, Tens, E-Stim, gentle stretching, hydrotherapy, body weight exercises, light intensity, breathing exercises, NO HIGH ALTITUDES

300

What is the physiology of GBS

Immune system (Macrophages and T Cells) attack myelin sheath. Myelin allows for conduction via saltatory propataion. Damage = slow conduction. 

400

Describe the levels of ambulation for (Hard one sorry.)

T4-T6

T9-T12

L1-L4

L4-5,

S1 below

T4-T6 - Standing frame or RGO 

T9-T12 - Household with B KAFO and AD

L1-L4 - Functional ambulation may need KAGO or AFO

L4-L5 - AFO (if no gastroc innervation) 

S1 and below - depends on weakness. 

400

What is cushings triad and what is that a sign of

Bradycardia, Systolic hypertension (Widening pulse pressure), and irregular respiration --> Increased ICP 

400

What is the criteria for diagnosing pots

HR >30 0r 40 within 10 minutes of standing (Focus on LE to enhance venous return and core strengthing for postural control.)

400

double question (Sorry) 1. What are the most common joints affected by hemophillia? 2. how do you treat hemophillia A vs Hemophillia B (Christmas disease)

1. Hinge joints (Knee, Elbow, Ankle)

2. Hemophillia A - Factor a, Hemophillia B - Factor 9

400

What is the treatment in the acute phase of GBS

Low resistance and avoid antigravity movmeent until MMT is at least 3/5, frequent rest, based on patient tolerance. 

500

What is a pivotal functional advantage at a C6 SCI 

Stability and power of the shoulder girdle in addition to wrist extension with tendonesis grasp. 

(Can achieve independence with sliding board to level surface, indepednet pressure relief with lateral or foward lean, males can be indepdent with bladder)

500

Describe the Ranchos levels (or write them on the board) 

1 - No response, total 

2 - Generalized, Total 

3 - Localized, Total

4 - Agitated confused, max 

5 - Inappropriate confused, max 

6 - Appropriate confused, Mod 

7 - Automatic, appropriate, min 

8 - Purposeful, appropriate, stand by 

500

What levels are high with Heterotopic Ossificans (HO). 

Alkaline Phosphatase

500

What types of exercises are beneficial for patients with hemophillia 

Gentle statis contraction, gentle stretching in pain free ROM. Hold relax. Active stretch is best, Passive is Okay. Serial splinting can also be used to prevent contracture. 
500

What are important things to invlude in screening for JIA 

Active screen, functional movement, temperature (systemic), palpation, effusion measurement, postural for joint deformities. Watch for AA instability. 

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