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Spinal Cord Injuries (SCI)
These are injuries to the spinal cord, vertebral column or intervertebral disc
A. Diaphragmatic movement and breathing
A client has an injury at C4. Which function is expected to be impaired?
A. Diaphragmatic movement and breathing
B. Bowel and bladder control
C. Hand grasp and wrist extension
D. Ambulation with long leg braces
Lumbar area
This area of spina cord innervates the bladder or legs
Answer: Cervical region
If a patient has quadriplegia/tetraplegia, which part of the spinal cord is affected?
Answer: C3–C5
If a patient has loss of diaphragmatic control, which level is injured?
abdominal
_______ muscle is essential for coughing reflex
Thoracic
This area of the spinal cord innervates abdominal and bowel movements
paralytic ileus
No bowel movement is also called ______
diaphragm and arms
The cervical area of the spinal cord innervates the ______ and the _______.
B. Respiratory paralysis
Rationale: The cervical level (especially C3–C5) innervates the diaphragm via the phrenic nerve. Damage can lead to respiratory failure/paralysis, which is life-threatening. Loss of bowel/bladder (A) is seen in thoracic/lumbar injury. Paraplegia (C) results from thoracic/lumbar injury. Abdominal muscle loss (D) is thoracic.
A client sustained a cervical spinal cord injury at C4. Which of the following complications is the nurse most concerned about?
A. Loss of bowel and bladder control
B. Respiratory paralysis
C. Paraplegia
D. Loss of abdominal muscle function
Answer: C. Loss of abdominal muscle control and bowel dysfunction
Rationale: Thoracic SCI affects abdominal muscles and bowel motility. Quadriplegia (A) is seen in cervical injuries. Respiratory paralysis (B) occurs in high cervical injuries. Arm paralysis (D) is cervical.
A nurse is caring for a patient with a thoracic spinal cord injury. Which assessment finding is expected?
A. Quadriplegia
B. Respiratory muscle paralysis
C. Loss of abdominal muscle control and bowel dysfunction
D. Flaccid paralysis of arms
x-ray
CT scan
CT Scan and X-ray are the primary tools for detecting skeletal injuries such as fractures or dislocations of the vertebral column.
MRI is preferred when assessing soft tissue and spinal cord damage.
EEG checks brain electrical activity (not spinal injury).
EMG evaluates muscle/nerve function, not bone integrity.
Lumbar puncture is for CSF analysis (e.g., meningitis, bleeding), not skeletal injury
These tests are utilize to diagnose if there is a skeletal injury in the back bone of the patient
prevent further injury
The general concept of emergency management for spinal cord injury is to “________.”
Answer: Spine board
A patient with suspected SCI must be immobilized on a flat, firm surface such as a ________.
Answer: Head, Neck
When immobilizing a patient with SCI, the ________ and ________ should be maintained in a neutral position.
Neutral
During transport of an SCI patient, the nurse should maintain the body in an ________ position.
Answer: Unit; realign
In SCI management, the patient should be transported as a ________ and the nurse should not attempt to ________ body parts.
Answer: False (This causes misalignment of the spine)
TRUE or FALSE: Placing a pillow under the head is recommended to keep the patient comfortable during SCI transport.
Meningitis
This is called the inflammation of the meninges
Streptococcus pneumoniae and Neisseria meningitis
Most common causative agent of meningitis
Answer: Blood-brain barrier (BBB)
In meningitis pathophysiology, the organism first crosses the ________ before reaching the cerebrospinal fluid.
Answer: Subarachnoid
The space between the arachnoid mater and the pia mater, where CSF circulates, is called the ________ space.
Fever and Headache
Altered level of Consciousness
Nuchal Rigidity
The classic triad of meningitis consists of:
headache and fever
Initial manifestations of meningitis
Kernig’s
________ sign is positive when pain and resistance occur upon flexion of the hip and knee, followed by extension of the leg.
neck
Brudzinski’s sign is positive when passive flexion of the ________ causes involuntary flexion of the hips and knees.
Answer: Meningeal irritation (Meningitis)
Both Kernig’s and Brudzinski’s signs are used to assess for ________.
supine
In Kernig’s sign, the patient is positioned ________ during the assessment.
Brudzinski’s
_______ sign is more sensitive indicator in assessing meningitis
Tic Douloureux
Trigeminal Neuralgia is most commonly known as ______
unknown
The cause of Trigeminal Neuralgia is _______
pain
The primary symptom of patient with trigeminal neuralgia is _____
Answer: Electric shock (or stabbing)
The hallmark symptom of trigeminal neuralgia is sudden, severe, ________-like facial pain.
painful twitching
Trigeminal Neuralgia’s presentation is p______ t_______.
Answer: Carbamazepine
The drug of choice for trigeminal neuralgia is the anticonvulsant ________.
Answer: Room (lukewarm/neutral)
During meals, patients with trigeminal neuralgia should eat soft foods at ________ temperature.
Answer: Lukewarm water
The nurse should advise the patient with Trigeminal Neuralgia to wash the face with ________ instead of cold water to avoid triggering pain.
Answer: Rhizotomy
If pharmacologic management for patient with Trigeminal Neuralgia fails, a surgical procedure that destroys part of the trigeminal nerve is called ________.
Bell’s Palsy
This condition involves facial paralysis
Answer: VII (Facial nerve)
Bell’s palsy is paralysis of the muscles innervated by cranial nerve number ________.
True
TRUE or FALSE: Bell’s palsy is caused by inflammation of the facial nerve, often linked to viral infections such as herpes simplex.
Answer: painful twitching; paralysis
The hallmark symptom of trigeminal neuralgia is facial ______, while the hallmark symptom of Bell’s palsy is unilateral facial ______.
TRUE
TRUE or FALSE: Neurodegenerative disorders involve permanent and irreversible damage
Parkinson’s Disease
This is a slow progressing neurologic movement disorder
Answer: Dopamine
Parkinson’s disease is caused by the degeneration of ______-producing neurons in the brain.
Substantia Nigra
The main problem in Parkinson’s Disease is the destruction of _____ which releases dopamine
Tremors
Rigidity
Akinesia/Bradykinesia
Postural Instability
Four Cardinal Signs of Parkinson’s Disease (TRAP)
Tremors
Earliest sign of Parkinson’s Disease
Answer: Levodopa (often combined with Carbidopa)
The most common drug used in Parkinson’s disease that is converted into dopamine in the brain is ______.
Answer: Shuffling gait
The typical Parkinson’s gait characterized by short, sliding steps is called ______ gait.
Answer: Propulsive gait
The ______ gait in Parkinson’s disease is associated with a stooped posture, making the patient look like they are falling forward.
Answer: Festinating gait
The ______ gait occurs when the patient involuntarily speeds up while walking and leans forward.
2 or more of the cardinal manifestation
Parkinson’s Disease is clinically diagnosed if __________ is present
Levodopa
A positive response to the medication ______ is often used as confirmatory diagnosis of Parkinson’s disease.
Carbidopa
This medication prevents breakdown of levodopa in the bloodstream
Multiple Sclerosis (MS)
This condition is characterized by the irreversible demyelinating disease of CNS
A. Diplopia
A nurse suspects MS in a patient who reports visual changes, muscle weakness, and problems with coordination. Which early visual symptom is MOST common?
A. Diplopia
B. Photophobia
C. Conjunctivitis
D. Ptosis
C. Exposure to heat and infection
The nurse is teaching a client with MS about factors that may trigger exacerbations. Which of the following should the nurse emphasize to avoid?
A. Cold environments
B. Increased sodium intake
C. Exposure to heat and infection
D. Low-fat diet
Charcot’s Triad
The pathognomonic sign of Multiple Sclerosis is also called _______
Scanning Speech
Intention Tremors
Nystagmus
Charcot’s triad in multiple sclerosis is composed of three pathognomonic sign (SIN) which are:
warm compress
A nurse is caring for a patient with multiple sclerosis who experiences spasticity. What is the most appropriate nursing management to minimize spasticity?
Guillain–Barré Syndrome
This is the autoimmune demyelination of the PNS
ascending (Galing-Baba-Syndrome)
The hallmark of Guillain–Barré Syndrome is progressive ______ paralysis.
False
Rationale:
GBS is usually an acute, reversible condition.
With proper management (IVIG, plasmapheresis, respiratory support, rehab), most patients recover fully or with minimal residual weakness.
Unlike Multiple Sclerosis (MS) or Amyotrophic Lateral Sclerosis (ALS), GBS does not cause permanent, progressive degeneration.
TRUE or FALSE: GBS is an irreversible disease
Viral infection
Antecedent event of Guillain–Barré Syndrome:
ascending paralysis
Pathognomonic sign of GBS
Neuromuscular Respiratory Failure
Most dangerous result of GBS which is why it is considered a medical emergency
Answer: False – Elective intubation is done before complete failure to prevent emergency intubation.
In Guillain–Barré Syndrome, elective intubation is performed once respiratory muscles are paralyzed and the patient is in respiratory arrest.
Myasthenia Gravis (MG)
This is an autoimmune disorder affecting the myoneural junction.
Answer: Anticholinesterase drugs (e.g., pyridostigmine) and Immunosuppressants (e.g., corticosteroids).
The two main medications used in the management of Myasthenia Gravis are ______ and ______.
Answer: Ptosis
A classic early sign of Myasthenia Gravis is drooping of the eyelids, also known as ______.
A. Myasthenic Crisis
During a Tensilon test, the patient’s muscle strength improves dramatically. This indicates:
A. Myasthenic Crisis
B. Cholinergic Crisis
C. Either one
D. Normal finding
B. Cholinergic Crisis
A nurse notes that a patient with MG has excessive salivation, diarrhea, and bradycardia after taking pyridostigmine. This is most likely:
A. Myasthenic Crisis
B. Cholinergic Crisis
B. An autoimmune destruction of acetylcholine receptors at the neuromuscular junction
Myasthenia gravis is primarily caused by:
A. A deficiency of dopamine in the brain
B. An autoimmune destruction of acetylcholine receptors at the neuromuscular junction
C. A lack of acetylcholine release from presynaptic neurons
D. Degeneration of motor neurons in the spinal cord
Answer: C. Ptosis and diplopia
What is usually the first clinical manifestation of Myasthenia Gravis?
A. Limb weakness
B. Respiratory distress
C. Ptosis and diplopia
D. Dysphagia
Answer: ocular; facial/bulbar; respiratory
The clinical progression of MG often begins with ______ involvement, followed by ______ weakness, then generalized weakness, and finally ______ compromise.
Edrophonium chloride (Tensilon)
Generic name of Tensilon in Tensilon Test
Atropine
This is the antidote for cholinergic crisis
Pyridostigmine bromide (Mestinon) and Neostigmin (Prostigmin)
First line of therapy for Myasthenia Gravis which inhibit breakdown of acetylcholine
Teaching focuses on strategies to conserve energy
Minimize risk of aspiration
Eye problems
Focus of nursing management for patients with Myasthenia Gravis
90 mins
Pyridostigmine bromide (Mestinon) and Neostigmin (Prostigmin)’s peak effect is ______ mins after administration.