Student Name
Western Governors University
D115 Advanced Pathophysiology for the Advanced Practice Nurse
Prof. Name:
Date
Meningitis is inflammation of the meninges (pia mater and arachnoid mater) surrounding the brain and spinal cord. It may be caused by bacteria, viruses, fungi, parasites, toxins, or noninfectious processes.
Most common bacterial causes:
Neisseria meningitidis (meningococcus)
Streptococcus pneumoniae (pneumococcus)
Drug-resistant strains are increasing
Highest risk: Infants <1 year, adolescents, adults >40
Common in congregate settings:
College dormitories
Military bases
Sub-Saharan Africa
Otitis media or sinusitis
Pneumonia
Immunocompromised state
Post-splenectomy or sickle cell disease (pneumococcal risk)
Respiratory droplets or saliva
Close contact: kissing, coughing, sneezing, sharing food/drinks
Asymptomatic carriers may transmit disease
Pathogens enter via respiratory tract, bloodstream, or neurosurgical procedures
Cross the blood-brain barrier → multiply in CSF
Toxins increase vascular permeability → cerebral edema
CSF obstruction → increased intracranial pressure (ICP)
Brainstem herniation may result in death
Systemic signs
Fever, chills, tachycardia
Meningeal signs
Severe headache
Photophobia
Nuchal rigidity
Positive Kernig and Brudzinski signs
Neurologic signs
Decreased level of consciousness
Seizures
Hemiparesis, hemiplegia, ataxia
Confusion
Projectile vomiting
Papilledema
Petechial or purpuric rash
Bulging fontanels (infants)
Opisthotonic posturing (children)
Lumbar puncture: ↑ WBCs in CSF
Blood cultures to identify organism
Immediate empiric IV antibiotics
Adjust therapy based on cultures
Dexamethasone for pneumococcal meningitis
Supportive care
Septic shock
DIC
Purpura fulminans
Multi-organ failure
Vaccinations:
Meningococcal
Pneumococcal
Haemophilus influenzae type B
An acute, immune-mediated demyelinating disorder of the peripheral nervous system causing ascending muscle weakness.
Often follows infection or immune activation:
Campylobacter jejuni
CMV, EBV
Influenza
Mycoplasma pneumoniae
Zika virus
Surgery, immunization
Molecular mimicry leads to antibodies attacking peripheral nerve myelin or axons
Complement activation disrupts nerve conduction
Acute inflammatory demyelinating polyneuropathy (most common)
Acute motor axonal neuropathy
Acute motor-sensory axonal neuropathy
Miller Fisher syndrome (rare)
Ascending flaccid paralysis
Paresthesia in hands and feet
Muscle weakness
Areflexia
Autonomic instability
Respiratory muscle paralysis (within 2 weeks possible)
Progressive weakness in ≥2 limbs
Areflexia
Progression ≤4 weeks
IV immunoglobulin (IVIG)
Plasmapheresis
Aggressive rehabilitation
Weeks to months (up to 2 years)
~30% have residual weakness
A chronic autoimmune demyelinating disease of the central nervous system.
T-cells cross the blood-brain barrier and attack myelin
Cytokine release damages oligodendrocytes
Demyelination → plaques visible on MRI
Early remyelination occurs but declines over time
Female sex
HLA-DR2 gene
Vitamin D deficiency
Geographic latitude (farther from equator)
Relapsing-remitting (most common)
Secondary progressive
Primary progressive
Progressive-relapsing
Motor: weakness, tremor, spasticity, ataxia
Sensory: numbness, paresthesia, Lhermitte sign
Visual: optic neuritis, diplopia
Speech: dysarthria
Autonomic: bowel/bladder dysfunction
Cognitive: depression, anxiety, impaired concentration
Charcot’s Triad
Dysarthria
Nystagmus
Intention tremor
MRI showing CNS plaques
CSF oligoclonal bands
Visual evoked potentials
Symptoms separated in time and space
Acute flares: corticosteroids, IVIG, plasmapheresis
Disease-modifying therapy: interferon-beta, immunosuppressants
Rehabilitation and symptom management
A chronic autoimmune disorder causing fluctuating skeletal muscle weakness due to impaired neuromuscular transmission.
Antibodies destroy acetylcholine receptors at the neuromuscular junction
Ptosis, diplopia
Facial weakness
Difficulty chewing, swallowing, speaking
Limb and neck weakness
Fatigue improves with rest
Acetylcholine receptor antibodies
Anti-MuSK antibodies
EMG
Edrophonium test
CT/MRI for thymoma
Anticholinesterase drugs
Immunosuppressants
Thymectomy
IVIG or plasmapheresis
A metabolic disorder characterized by chronic hyperglycemia due to insulin deficiency or resistance.
Insulin ↓ blood glucose
Glucagon ↑ blood glucose
Produced in pancreatic islets
Autoimmune destruction of β-cells
Absolute insulin deficiency
Associated with HLA-DR3 and DR4
Classic Symptoms
Polyphagia
Polyuria
Polydipsia
Glycosuria
Complication
Diabetic ketoacidosis (DKA)
Treatment
Lifelong insulin therapy
Insulin resistance
Relative insulin deficiency
Strongly associated with obesity and genetics
Complication
Hyperosmolar hyperglycemic state (HHS)
Treatment
Lifestyle modification
Oral antidiabetic drugs (e.g., metformin)
Insulin if needed
Fasting glucose ≥126 mg/dL
Random glucose ≥200 mg/dL
OGTT ≥200 mg/dL at 2 hours
HbA1c ≥6.5%
Excess secretion of parathyroid hormone causing hypercalcemia.
Primary: Parathyroid adenoma or hyperplasia
Secondary: Chronic hypocalcemia (CKD, vitamin D deficiency)
Tertiary: Autonomous PTH secretion after long-standing secondary disease
Kidney stones
Bone pain, fractures, osteoporosis
GI symptoms (constipation, nausea)
Neuropsychiatric symptoms
Polyuria, polydipsia
Surgical removal (primary)
Calcimimetics (cinacalcet)
Vitamin D and phosphate management (secondary)
Autoimmune stimulation of TSH receptors
Symptoms: weight loss, tremor, anxiety, heat intolerance
Labs: ↓ TSH, ↑ T3/T4
Treatment: antithyroid drugs, beta-blockers, surgery
Life-threatening thyrotoxicosis
Triggered by stress or surgery
Requires ICU management
Autoimmune destruction of thyroid
Symptoms: fatigue, weight gain, cold intolerance
Treated with levothyroxine
Inflammation of the middle ear, primarily in children.
Reduced tympanic membrane mobility
Tympanometry or pneumatic otoscopy
First-line: high-dose amoxicillin
Watchful waiting recommended for mild cases
≥2 weeks of depressed mood or anhedonia
Treated with SSRIs, psychotherapy, or combination
Excessive worry ≥6 months
Treated with CBT and SSRIs/SNRIs
Psychotic disorder with positive, negative, and cognitive symptoms
Treated with antipsychotics and psychosocial therapy
Post Categories
Tags