Meningitis Inflammation of the meninges, usually resulting from an infection CSF may also become...

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Meningitis • Inflammation of the meninges, usually resulting from

an infection

• CSF may also become affected

• Causes: bacteria (e.g., Neisseria meningitidis, Streptococcus pneumoniae, and Haemophilus influenzae), viruses (e.g., enterovirus, measles, influenza, and herpes), tumors, and allergens

• Infection or irritant triggers the inflammatory process, leading to swelling of the meninges and increased ICP

• Risk factors: being less than 25 years of age, living in a community setting, pregnancy, working with animals, and immunodeficiency

Meningitis • Can be self-limiting (viral) or life-threatening (acute

bacterial)• Complications: permanent neurologic damage, seizures,

hearing loss, blindness, speech difficulties, learning disabilities, behavior problems, paralysis, renal failure, adrenal gland failure, shock, and death

• Manifestations: fever, chills, mental status changes, nausea, vomiting, photophobia, severe headache, stiff neck (meningismus), agitation, bulging fontanelle, decreased consciousness, opisthotonos (abnormal positioning that involves rigidity and severe arching of the back with the head thrown backward), poor feeding or irritability in children, tachypnea, and rash

Meningitis

• Diagnosis: history, physical examination, throat cultures, lumbar puncture with CSF analysis, polymerase chain reaction test, and head computed tomography

• Treatment: antibiotics (if bacterial), hydration, fever management, and vaccinations (prevention)

Encephalitis• Inflammation of the brain and spinal cord, usually

resulting from an infection• Causes: virus (e.g., coxsackievirus, echovirus, poliovirus,

adenovirus, herpes virus, cytomegalovirus, Eastern equine encephalitis virus, West Nile virus, St. Louis virus, measles, and mumps) and bacterial infections (e.g., Lyme disease, tuberculosis, and syphilis)

• Infection triggers the inflammatory response that causes vasodilatation, increased capillary permeability, and leukocyte infiltration

• The inflammatory process can cause nerve cell degeneration and diffuse brain destruction

Encephalitis

• May be primary (direct viral infection of the brain and spinal cord) or secondary (travels from elsewhere in the body)

• Most cases are mild and self-limiting, but can be severe and life threatening

• Vulnerable groups to more severe progression: immune compromised persons, young children, older adults, those living in high-incidence areas, and those frequently outdoors

• Complications: cerebral edema, cerebral hemorrhage, and brain damage

Encephalitis Manifestations• Result from meningeal irritation and neurologic

damage.• Similar to meningitis but with a more gradual

onset• Most cases are mild and go undetected• Include: flulike symptoms, headache, neck

rigidity, confusion, hallucinations, personality changes, diplopia, seizures, muscle weakness, paresthesia or paralysis, loss of consciousness, tremors, abnormal deep tendon reflexes, rash, and bulging fontanel

Encephalitis

• Diagnosis: history, physical examination, head computed tomography, head magnetic resonance imaging, electroencephalogram,  lumbar puncture with CSF analysis, polymerase chain reaction test, and serum viral antibodies

Encephalitis Treatment

• Usually self-limiting, requiring no treatment

• Rest

• Adequate nutrition, including plenty of liquids

• Reorientation and emotional support

• Analgesics and antipyretics to relieve headaches and fever

• Antiviral agents (if viral)

Encephalitis Treatment• Antibiotic therapy (if bacterial)

• Corticosteroids to reduce cerebral edema

• Antiseizure agents

• Sedatives to treat irritability and restlessness

• Physical, speech, and occupational therapy

• Prevention: vaccinations, wearing protective clothing, using mosquito repellant, and eliminating water sources

Traumatic Brain Injury • Usually caused by a sudden and violent blow or jolt to the

head (closed injury) or a penetrating (open injury) head wound that disrupts the normal brain function

• The injury can bruise the brain, damage nerve fibers, and cause hemorrhaging

• Causes: falls, motor vehicle accidents, penetration of an object, and assaults

• Vary from mild to severe

• Persons at highest risk: males, children 0–4-year-olds, adolescents 15–19-year-olds, adults 75 years of age or older, certain military personnel (e.g., paratroopers), and African Americans (highest death rates)

Traumatic Brain Injury

• Complications: – Can occur from one significant event or multiple mild

events

– Changes in thinking, sensation, language, or emotions

– Seizures

– Alzheimer’s disease

– Parkinson’s disease

– Memory decline

– Depression

– Death

Traumatic Brain Injury • Conditions associated with closed TBIs

– Concussion – momentary interruption of brain function• Usually results from a mild blow to the head

that causes sudden movement of the brain, disrupting neurologic functioning

• May or may not lead to a loss of consciousness

• Amnesia, confusion, sleep disturbances, and headaches may occur for weeks or months

Traumatic Brain Injury

• Conditions associated with closed TBIs – Cerebral contusion – bruising of the brain

• Most result from a blunt blow that causes the brain to make sudden impact with the skull

• Coup – initial area brain impacts with skull• Countercoup – area opposite side of the brain where

it rebounds and impacts with skull • Vary in severity depending on the extent of damage

and the amount of bleeding• Residual effects depend on severity

Traumatic Brain Injury

• Conditions associated with open TBIs – Fractures – may be a linear skull

fracture, a comminuted skull fracture , a compound skull fracture, a depressed skull fracture, or a basilar skull fracture

– Infections

Traumatic Brain Injury Manifestations

• May be vague and develop slowly, or they may be sudden and severe

• Symptoms may improve and then suddenly worsen

• The outward appearance of the head is not an indication of the injury severity

Traumatic Brain Injury Manifestations

• Not being able to recall event details

• Indications of a concussion

• Changes in or unequal pupil size

• Seizures

• Asymmetrical facial features

• Fluid draining from the nose, mouth, or ears

• Fracture in the skull or face

• Bruising of the face

• Swelling at the site of the injury

• Scalp wound

• Impaired hearing, smell, taste, speech, or vision

Traumatic Brain Injury Manifestations

• Inability to move one or more limbs

• Irritability (especially in children)

• Personality changes• Unusual behavior• Loss of

consciousness

• Bradypnea • Hypotension• Restlessness• Lack of coordination• Lethargy• Stiff neck• Vomiting

Traumatic Brain Injury

• Diagnosis: history, physical examination (including using the Glasgow Coma scale), head computed tomography, head magnetic resonance imaging, and ICP  monitoring

• Treatment: rest, analgesics (specifically acetaminophen [Tylenol]), cold compresses, osmotic diuretics (e.g., mannitol), antiseizure agents, sedatives, surgery, rehabilitation (e.g., physical, speech, and occupational therapy)

Traumatic Brain Injury Prevention• Wearing a seat belt when driving or riding in a motor

vehicle• Using appropriate child safety seats, wearing a helmet

when appropriate (e.g., when playing sports, riding a bicycle, or skating)

• Making the home safe (e.g., removing tripping hazards, having adequate lighting, using safety gates)

• Storing firearms in locked cabinets• Never driving impaired• Supervising children when playing

Increased Intracranial Pressure

• Increased volume in the cranial cavity• Causes: traumatic brain injury, tumor,

hydrocephalus, cerebral edema, and hemorrhage

• Monro-Kellie hypothesis - increase in volume of one component must be compensated by a decrease in volume of another.– Accomplished mostly by shifts in the CSF and

blood volume

Manifestations of Increased Intracranial Pressure

• Generally manifestations include: decreasing level of consciousness, vomiting (often projectile), increasing blood pressure with increasing pulse pressure, bradycardia, papilledema, fixed and dilated pupils, and posturing

• Manifestations in infants include: separated sutures and bulging fontanelle

• Manifestations in older children and adults include: behavior changes, severe headache, lethargy, neurologic deficits, and seizures

Increased Intracranial Pressure

• Diagnosis: history, physical examination (including completing the Glasgow Coma scale), head computed tomography, head magnetic resonance imaging, and ICP monitoring

• Treatment: depends on the underlying etiology (e.g., remove tumor or blood), respiratory support, semi-Fowler’s positioning, draining excess CSF, osmotic diuretics, corticosteriods, seizure precautions, antiseizure agents, sedatives, stool softeners, antiulcer agents, thermoregulation, and glucose management

Spinal Cord Injuries

• Result from direct injury to the spinal cord or indirectly from damage to surrounding bones, tissues, or blood vessels

• Causes: motor vehicle accidents, falls, violence, sports injuries, and weakening vertebral structures (e.g., rheumatoid arthritis or osteoporosis)

• Direct damage can occur if the spinal cord is pulled, pressed sideways, or compressed – This damage may occur if the head, neck, or back

twists abnormally during an accident or injury

Spinal Cord Injuries

• Hemorrhage, fluid accumulation, and edema can occur inside or outside the spinal cord (but within the spinal canal)

• The accumulation of blood or fluid can compress the spinal cord and damage it

• Spinal shock – temporary suppression of neurologic function because of spinal cord compression; neurologic function gradually returns

• Most common in Caucasians and males, with 40.2 years being the average age at injury

Spinal Cord Injury Complications• Loss of neurologic functioning• Varying degrees of paralysis• Cauda equina syndrome – injury to the nerve roots in

the area of the cauda equina• Autonomic hyperreflexia - a massive sympathetic

response that can cause headaches, hypertension, tachycardia, seizures, stroke, and death; most commonly associated with injuries above T6

• Neurogenic shock – an abnormal vasomotor response secondary to disruption of sympathetic impulses

Spinal Cord Injury Complications

• Respiratory failure • Effects of immobility (e.g., constipation,

pulmonary infections, urinary infections, thrombus, impaired skin integrity, contractures)

• Changes in bowel and bladder function • Sexual dysfunction • Chronic pain• Death

Spinal Cord Injury Manifestations• Cervical injuries can affect both the upper and

lower extremities and include: breathing difficulties, loss of normal bowel and bladder control, paresthesia, sensory changes, spasticity, pain, weakness, paralysis, blood pressure instability, temperature fluctuations, and diaphoresis

• Thoracic injuries affect the lower extremities, and the manifestations can be the same as those for cervical injuries

• Lumbar sacral injuries can affect the lower extremities in varying degrees, and manifestationsn are similar to those of cervical injuries, with the exception of breathing difficulties

Spinal Cord Injuries

• Diagnosis: history, physical examination (including a neurologic assessment), spinal computed tomography, spinal magnetic resonance imaging , spinal X-ray, and spinal myelogram

 

Spinal Cord Injury Treatment

• Immediate:

– Immobilization of the spine

– Corticosteroid agents to reduce swelling

– Spinal traction to reduce the fracture and immobilize the spine

– Surgical repair of vertebral fractures or surgical removal of the fluid compressing the spinal cord (decompression laminectomy)

– Respiratory management

– Bed rest

• Long-term:

– Physical, occupational, and speech therapy

– Mobility assistive devices

– Long-term respiratory management

– Meticulous skin care

– Bowel and bladder training or management

– Antispasmotic agents and botulinum toxin type A (Botox) injections to treat muscle spasms

– Pain management

– Nutritional support

– Prompt treatment of infections  

Transient Ischemic Attack • A temporary episode of cerebral ischemia that

results in symptoms of neurologic deficits

• Also called ministrokes because these neurologic deficits mimic a cerebral vascular accident (CVA) or stroke except that these deficits resolve within 24 hours (1–2 hours in most cases)

• May occur singly or in a series

• Warning signs that a CVA may be impending; however, not all CVAs are preceded by a TIA

Transient Ischemic Attack

• Ischemia can occur because of a cerebral artery occlusion (e.g., thrombus, embolus, or plaque), cerebral arteries narrowing (e.g., atherosclerosis, or spasms), or cerebral artery injury (e.g., inflammation, or hypertension)

• Additional risk factors: migraines, smoking, diabetes mellitus, advancing age, inadequate nutrition, hypercholesterolemia, oral contraceptive usage, excessive alcohol consumption, and illicit drug use

• Complications: permanent brain damage, injury from falls, and CVA

Transient Ischemic Attack Manifestations

• Begin suddenly and last for a short period• Manifestations are the same as for a stroke• Reflect the location of the ischemia

Transient Ischemic Attack Manifestations

• Muscle weakness or paralysis of the face, arm, or leg (usually unilateral)

• Unilateral paresthesia

• Aphasia or receptive aphasia

• Dysphagia

• Dysgraphia

• Difficulty reading

• Vision issues (e.g., diplopia, nystagmus, and partial or complete loss of vision)

• Changes in sensation (e.g., touch, pain, temperature, pressure, hearing, and taste)

• Change in levels of consciousness

• Personality, mood, or emotional changes

• Confusion

• Agnosia (inability to recognize or identify sensory stimuli)

• Ataxia

• Vertigo or dizziness

• Incontinence of bowel or bladder

Transient Ischemic Attack

• Diagnosis: history, physical examination (including a neurologic assessment and blood pressure), head computed tomography, head magnetic resonance imaging, carotid ultrasound, cerebral arteriogram, electroencephalogram, serum clotting studies, blood chemistry, complete blood count, erythrocyte sedimentation rate test, and serum lipids test

• Treatment: manage any underlying conditions, antiplatelet aggregation agents, anticoagulants, angioplasty, carotid endarterectomy, smoking cessation, minimizing dietary cholesterol and fat, increasing dietary fruits and vegetables, exercising regularly, limiting alcohol consumption, and eliminating illicit drug use

Cerebral Vascular Accident

• AKA stroke or brain attack• An interruption of cerebral blood supply • Ischemic damage is permanent• Causes: total vessel occlusion (e.g., thrombus,

embolus, or plaque) or cerebral vessel rupture (e.g., cerebral aneurysm, arteriovenous malformation, or hypertension)

• Major types of CVA– Ischemic strokes are the most common – Hemorrhagic strokes are the most deadly

Cerebral Vascular Accident

• Complications: neurologic deficits and death

• Most common in African Americans and those living in the Southeast region

• Additional risk factors: physical inactivity, obesity, hypertension, smoking, hypercholesterolemia, diabetes mellitus, atherosclerosis, oral contraceptive usage, excessive alcohol consumption, and illicit drug use

Cerebral Vascular Accident

• Manifestations are similar those of a TIA except that CVA symptoms do not resolve

• Manifestations may improve with time and therapy, but they can remain, creating complications

• Additional manifestations, headaches may be present with hemorrhagic strokes because of increasing ICP

Cerebral Vascular Accident

• Diagnosis: history, physical examination (including a neurologic assessment), head computed tomography, head magnetic resonance imaging, carotid ultrasound, cerebral arteriogram, serum clotting studies, blood chemistry, and complete blood count

Cerebral Vascular Accident Treatment

• Requires prompt treatment to minimize brain damage• Determining whether the CVA is ischemic or hemorrhagic in origin

prior to treatment • Treatment should be delivered within 3 hours of symptom onset• Ischemic strokes: thrombolytic agents, aspirin, angioplasty, carotid

endarterectomy • Hemorrhagic strokes: surgical repair of aneurysms or arteriovenous

malformations as well as blood removal • Corticosteroids and antihypertensive may be administered with either

type• Multidisciplinary team management• Strategies to prevent complications of immobility

Cerebral Aneurysm

• A localized outpouching of a cerebral artery due to weakening of the artery wall

• Causes: congenital defects, hypertension, connective tissue diseases (e.g., Marfan syndrome), traumatic brain injuries, and arterial wall infections

• Can put pressure on surrounding tissue as well as leak or rupture, causing a CVA or death

• Most are berry or saccular • Most frequently occur in multiples on the circle

of Willis

Cerebral Aneurysm

• Many are asymptomatic until they grow large enough to compress surrounding structures or ruptures

• Manifestations: vision issues (e.g., diplopia and loss of vision), headache, eye pain, and neck pain

• A sudden, severe headache is an indication that the aneurysm has ruptured; may also resemble those of increased ICP and CVA

Cerebral Aneurysm

• Diagnosis: history, physical examination, cerebral arteriography, head computed tomography, head magnetic resonance imaging, and electroencephalogram

• Treatment: surgical repair (if possible), managing contributing factors, and strategies similar to those for a CVA and subarachnoid hemorrhage

Seizure Disorder

• Seizure – transient physical or behavior alteration that results from an abnormal electrical activity in the brain

• Causes: altered membrane ion channels, altered extracellular electrolytes, and imbalanced excitatory and inhibitory neurotransmitters

• Can occur secondary to trauma, hypoglycemia, electrolyte disorders, acidosis, infection, tumors, or chemical ingestion (e.g., medications, illicit drugs, and alcohol)

Seizure Disorder

• Epilepsy – seizures disorder resulting from spontaneous firing of abnormal neurons and is characterized by recurrent seizures for which there is no underlying or correctable cause

• Complications: brain damage, traumatic brain injury, aspiration, mood disorders, and status epilepticus (seizures that last longer than 20 minutes or subsequent seizures occur before the individual has fully regained consciousness)

Seizure Disorder

• Two broad categories—focal and generalized

• Not all can be easily defined as either focal or generalized

• Some begin as focal seizures but then spread to the entire brain

• Other people may have both types of seizures but with no clear pattern

Focal Seizure• Also called partial seizures• Occur in just one part of the brain• Vary depending on the area of the brain affected• Simple focal seizure – individual remains conscious

but experiences unusual feelings or sensations that can take many forms (e.g., sudden and unexplainable feelings of joy, anger, sadness, or nausea; hear, smell, taste, see, or feel things that are not real)

• Complex focal seizure – individual has changes in or loss of consciousness, producing a dreamlike experience; may display strange, repetitious behaviors (e.g., blinking, twitching, moving one’s mouth, walking in a circle) called automatisms

Focal Seizure• Usually last just a few seconds• Some people may experience auras

(unusual sensations just prior to an impending seizure) that are actually simple focal seizures in which the person maintains consciousness

• Seizure characteristics tend to be similar with every seizure

• Can easily be confused with other disorders (e.g., migraine headaches, narcolepsy, syncope, and psychiatric disorders)

Generalized seizures • Abnormal neuronal activity on both sides of the

brain• May cause loss of consciousness, falls, or

massive muscle spasms• Absence seizure (previously called a petit mal

seizure) – individual may appear to be staring into space and/or have jerking or twitching muscles

• Tonic seizure – causes stiffening of muscles of the body, generally those in the back and extremities

• Clonic seizure – causes repeated jerking movements of muscles on both sides of the body

Generalized seizures

• Clonic seizure – causes repeated jerking movements of muscles on both sides of the body

• Myoclonic seizure – causes jerks or twitches of the upper body, arms, or legs

• Atonic seizure - causes a loss of normal muscle tone; will fall down or may drop his or her head involuntarily

• Tonic-clonic seizure (previously called grand mal seizures) –causes stiffening of the body and repeated jerks of the arms and/or legs as well as loss of consciousness

• Postictal period – just after the seizure, the individual may be confused, fatigued, and fall into a deep sleep

Seizure Disorder

• Diagnosis: history (including a description of the seizure activity if possible), physical examination, head computed tomography, head magnetic resonance imagining, head positron emission tomography, and electroencephalogram

Seizure Disorder

• Treatment– During a seizure, positioning the individual on his

or her side, protect head, do not force items in between the individual’s teeth, do not restrain the individual, manage airway, oxygen therapy, muscle relaxants, antiseizure agents, and allow to sleep following the seizure

– For epilepsy, antiseizure agents, surgical resection or transaction, wear a medical-alert bracelet, and avoid precipitating factors (e.g., sleep deprivation, alcohol, illicit drugs, and excessive stimuli)

Multiple Sclerosis

• Debilitating autoimmune condition that involves a progressive and irreversible demyelination of brain, spinal cord, and cranial nerves neurons

• Damage occurs in diffuse patches throughout the nervous system and slows or stops nerve impulses

• Progression of the damage varies • Most common in women, Caucasians, and those

living in temperate climates• The onset of symptoms usually occurs between

20 and 40 years of age• Complications: epilepsy, paralysis (most often the

legs), and depression

Multiple Sclerosis Manifestations

• Vary depending on the degree of damage and the specific nerves affected

• Characterized by remissions and exacerbations

• Exacerbations may last for days to months

• Fever, hot baths, sun exposure, and stress can trigger or worsen these episodes

• May progress without remissions

Multiple Sclerosis Manifestations • Fatigue

• Loss of balance

• Muscle spasms

• Paresthesia or abnormal sensation in any area

• Problems moving arms or legs

• Weakness in one or more arms or legs

• Unsteady gait

• Lack of coordination

• Tremor in one or more arms or legs

• Constipation and stool leakage

• Urinary frequency, urgency, hesitancy, or incontinence

• Vision issues (e.g., diplopia and vision loss)

• Decreased attention span, poor judgment, and memory loss

• Difficulty reasoning and solving problems

• Dizziness

• Hearing loss

• Sexual dysfunction

• Slurred speech

• Dysphagia

Dementia

• A group of conditions in which cortical function is decreased, impairing cognitive skills and motor coordination

• Issues with memory are common and include short-term memory losses as well as confusion of historical events

• Behavioral and personality changes interfere with relationships, work, and activities of daily living

• Causes: vascular disease (e.g., atherosclerosis), infections, toxins, and genetic conditions

• Types: Alzheimer’s disease, Creutzfeldt-Jakob disease, and AIDS dementia complex

• An elderly client is being admitted to the ICU with the diagnosis of a stroke. The nurse realizes that based upon this client's age, the most likely causes of the condition would be:

• Thrombosis.

• Pneumonia. • Hypertension. • Intracranial hemorrhage. • Post myocardial infarction.

Decreased cardiac output.

Alzheimer’s Disease

• Most common form of dementia• Brain tissue degenerates and atrophies, causing a steady

decline in memory and mental abilities• The exact etiology is unknown, but associated with three

pathologic characteristics– Amyloid plaques mix with a collection of additional

proteins, neuron remnants, and other nerve cell pieces– Neurofibrillary tangles – abnormal collections of a protein

called tau that clumps together– Connections between neurons responsible for memory

and learning are lost; neurons cannot survive when their connections to other neurons are lost

Alzheimer’s Disease

• Not a part of normal aging, but risk increases with age • Rates are higher in women• Rates may be higher in those persons with less

education for unknown reasons• Additional risk factors: family history, hypertension,

hypercholesterolemia, diabetes mellitus, and history of traumatic brain injury

• Complications: infections (primarily pneumonia and urinary tract infections), injuries related to falls, malnutrition, dehydration, and decubitus ulcers

Alzheimer’s Disease Manifestations

• Insidious onset

• Course may extend 10–20 years

• Include: memory loss, problems with abstract thinking, difficulty finding the right word to express thoughts or even follow conversations, difficulty reading and writing, disorientation (even in familiar surroundings), loss of judgment, difficulty performing familiar tasks, personality changes, hallucinations, and incontinence of bowel or bladder

Alzheimer’s Disease

• Diagnosis is often difficult and often involves ruling out other conditions

• Diagnosis: history, physical examination (including a neurologic assessment and mental status evaluation), head computed tomography, head magnetic resonance imaging, and head positron emission tomography

Alzheimer’s Disease

• Treatment:– No cure for AD, nor are there any therapies that

will slow the progression– Medications to manage symptoms and maximize

functioning: cholinesterase inhibitors (e.g., donepezil [Aricept], rivastigmine [Exelon], and galantamine [Razadyne]), memantine (Namenda), vitamin E, ginkgo, and Huperzine A

– Other strategies: memory aids (e.g., calendars), nutritional support, physical exercise, cognitive activities, safety precautions (e.g., supervision and removing clutter), maintaining a calm environment, social interactions, coping strategies, and support

Brain Tumors

• May be malignant or benign

• Can be life threatening because due to increased ICP and difficult to access

• May be primary, but most are secondary tumors (most commonly breast cancer, colon cancer, kidney cancer, lung cancer, melanoma, and sarcoma)

Brain Tumors

• Primary tumors are thought to arise from genetic mutations

• Risk factors for primary tumors: advancing age and exposure to radiation and occupational chemicals

• Prevalence and mortality rates highest among Caucasians and males

• Complications: neurologic deficits, seizures, personality changes, and death

Brain Tumors Manifestations• Vary depending on size and location

• Include:

– New onset or change in pattern of headaches

– Headaches, increasing frequency and severity

– Unexplained nausea or vomiting

– Vision problems

– Gradual loss of sensation or movement in an extremity

– Balance difficulties

– Speech difficulties

– Confusion

– Hearing problems

– Hormonal (endocrine) disorders

Brain Tumors

• Diagnosis: history, physical examination (including a neurologic assessment), head magnetic resonance imaging, biopsy, and other tests to determine cancer histology

• Treatment:– Depends on the size and location – Surgical, radiation, and chemotherapy– Rehabilitation including physical,

occupational, and speech therapy

• An elderly client is being admitted to the ICU with the diagnosis of a stroke. The nurse realizes that based upon this client's age, the most likely causes of the condition would be:

• Thrombosis.

• Pneumonia. • Hypertension. • Intracranial hemorrhage. • Post myocardial infarction. Decreased cardiac output.

• The elderly are more likely to develop thrombotic or hemorrhagic strokes.

• Diagnosis; Physiological Integrity; Application

• A male client is having a tonic-clonic seizures. What should the nurse do first?a. Elevate the head of the bed.b. Restrain the client’s arms and legs.c. Place a tongue blade in the client’s mouth.d. Take measures to prevent injury.