CE Summer Emergencies, Pacemakers, Quick Trach

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Summer Emergencies
Pacemakers
Quick Trach
APRIL 2015 CE
CONDELL MEDICAL CENTER
EMS SYSTEM
SITE CODE: 107200E-1215
Prepared by: Sharon Hopkins, RN, BSN
1
Revised 4.16.15
Objectives
Upon successful completion of this module, the EMS
provider will be able to:
1. Distinguish the difference between heat cramps, heat exhaustion,
and heatstroke.
2. List the steps of assessment for the patient involved in water emergencies.
3. Analyze signs and symptoms to determine the level of allergic reaction a
patient is experiencing.
4. Actively participate in review of selected Region X SOP’s as
related to the topics presented.
2
Objectives cont’d





5. Review pacemaker rhythms.
6. Actively participate in case scenario discussion.
7. Actively participate at the paramedic level in return
demonstration of insertion of the Quick Trach.
8. Actively participate in ventilating a manikin at the
appropriate ventilation rate for the situation.
9. Successfully complete the post quiz with a score of 80% or
better.
3
Thermoregulation

The ability to maintain or regulate a steady body
temperature despite changes to the environment
 Hypothalamus
at base of brain regulates temperature

You can lose or gain heat from and within the body
itself

You can lose or gain heat by contact with the external
environment

The body’s core/normal temperature of deep tissues
is normally 370C or 98.60F
4
Converting
Temperatures
 0F
= 9/5 0C + 32
 0C
= 5/9 (0F – 32)
5
Thermal Gradient

The difference in temperature between the
environment (also called the ambient
temperature) and the body

Heat flows from the warmer environment (higher
temp) to the cooler environment (lower temp)

Wind and relative humidity (percent of water
vapor in the air) affect heat gain and loss
6
Process of Transferring Heat

Conduction
 Direct

contact of one surface with another
Convection
 Heat
loss to air currents passing over the body
 Heat
must be conducted and exposed to the air before
being carried away by convection

Radiation
 Heat
loss via infrared rays
 Exposed
body could lose 60% of total body heat in
environment with normal room temperature
7
Transfer of Heat cont’d

Evaporation
 Change
 Water
 Heat
of a liquid to a vapor
or sweat evaporates from skin
loss is great via evaporation of fluids from the
lungs
 Normal
water loss from the skin and lungs is
approximately 600 ml per day
8
Transfer of Heat cont’d

Respiration
 Combines
the mechanics of convection, radiation, and
evaporation
 Accounts
for a large proportion of heat loss
 Heat
transfers from body to inspired air via convection
and radiation
 Evaporation
process in lungs humidifies inspired air
 During
expiration, humidified air released to the
environment creating on-going heat loss
9
Measuring Body Temperatures

By touch – get a sense of cool, warm, hot

Oral – normal 98.60F (370C)

Rectal – 0.5 – 10F higher than oral

Tympanic – 0.5 – 10F higher than oral

Axillary – 0.5 – 10F lower than oral

Core – area where most major organs are located
 In
the field tympanic (ear) or rectal
 In
the hospital bladder, heart with use
of special catheters/measuring tools
10
Homeostasis

Process of maintaining constant suitable conditions

Body functions within small ranges of “normal”

Hypothalamus at base of brain responsible for
temperature regulation (i.e.: the “thermostat”)

Body constantly compensating to maintain “normal”
 Core
and peripheral temperatures
 Oxygen
 Energy
levels
supplies
11
Homeostasis of Core Temperature

Body continually adjusting metabolic rate
 The
rate in which the body consumes energy to
maintain function required at the time
 Energy

production = heat production
Temperature controlled by dilating or constricting
blood vessels
 Dilation
of blood vessels – flushed skin
 Constriction
of blood vessels – pale skin
12
Temperature Control

To decrease the body temperature
 Blood
vessels dilate to expose more vessel surface
space to the skin
 Excess
heat carried from core to the periphery close to
the skin; heat dissipates from skin to environment

To increase body temperature
 Blood
vessels constrict to shunt warm blood away from
superficial veins near skin and back into deeper veins
near the core
 Shivering
heat
increases the metabolic rate and generates
13
Risk Factors Impacting Environmental Illness

Age
 Especially
very young and elderly

Poor general health

Fatigue

Predisposing medical conditions (i.e.: Diabetes – damages
autonomic nervous system & interferes with
thermoregulatory input)

Certain meds – prescription and OTC

Level of acclimatization – adjustment to the environment
14
Factors Influencing Impact of
Environmental Challenges

Length of exposure

Intensity of exposure

Environmental factors
 Humidity
 Wind
– influences evaporation rate
– influences convection
15
Heat Emergencies - Hyperthermia

Condition involving unusually high body core
temperatures

Usually involves a transfer of heat from the
external environment
 Could
include excessive heat production within the
body

Could occur with use/abuse of certain
medications
 Malignant
hyperthermia is a severe response to use
of certain anesthetics
16
Eliminating Excessive Heat

Body’s attempt to eliminate excessive heat:
 Diaphoresis
– due to sweating mechanism
 Evaporation

process to reduce the temperature
Increased skin temperature to touch – due to
vasodilation
 Moves
more blood volume to the skin surface to
induce radiation, conduction, convection

Flushing due to vasodilation process
17
Heat Cramps / Muscle Cramps

Caused by overexertion and dehydration in high
temperature situations

Sweating is a response to lower the body temperature
 Sodium
(salt) is transported to the skin
 Water
follows sodium
 Water
on skin surface cools body via evaporation
18
Heat Cramps cont’d
 Loss
of electrolytes due to sweating
 Can
cause intermittent skeletal muscle
cramping
Extremities
Abdominal
muscles
 Patient
generally remains alert and
complains of weakness
19
Heat Cramp Signs and Symptoms

Dizziness

Syncope/near-syncope

Stable vital signs

Body temperature normal or slightly elevated

Skin moist and warm
20
Treatment Heat Cramps

Consider what is making the patient symptomatic

Aim your therapy at the source of the problem
 Remove
from the offending environment
 Remove
clothing as necessary to facilitate cooling
 Patient
education goals
 Cooling
techniques
 Appropriate
hydration guidelines
21
Heat Exhaustion
An acute reaction to
heat exposure

The most common heat emergency

Patient can lose 1-2 L of fluid per hour
 Loses

sodium and water
Dehydration and electrolyte loss from sweating
often account for the signs and symptoms noted
22
Heat Exhaustion – Body Responses

General vasodilation
 Pooling
of blood volume mimics a decrease in
blood volume
 Leads
to a decrease in cardiac output

History of exposure to a heated environment
helps with the diagnosis

If treatment is not instituted, the patient may
progress to heat stroke
23
Signs and Symptoms Heat Exhaustion
Increased body temperature (>37.80C / 1000F)
or
 Cool and clammy with heavy perspiration


Rapid and shallow respirations

Weak pulse

Diarrhea

Muscle cramps

Weakness

May have loss of consciousness
24
Forming Your General Impression

History and assessment very important
 Need
clues to determine a working diagnosis to
know which treatment plan to institute

In the presence of the following CNS signs &/or
symptoms consider interventions for heat stroke

Headache
 Anxiety

Paresthesia - pins and needles sensation

Impaired judgment
 Psychosis
25
Treatment Heat Exhaustion

Move to a cooler environment

Remove as much clothing as possible, as indicated

Begin to fan the patient -  air currents (convection)

Keep patient supine

IV fluid challenge
 Adult:
200 ml increments; titrated with frequent
reassessments
 Note:
 Peds:
adult formula also calculated at 20 ml/kg
20ml/kg; repeat to max of 60 ml/kg; titrated
26
Heatstroke

True environmental emergency

Hypothalamic temperature regulation lost

Hyperthermia leads to cell death and damage to
brain, liver, kidneys

Indications of heat stroke
 Central
 Body
nervous system imbalance
temperature usually >1050F (40.60C)
 Absence
of sweating
27
Heatstroke –
Hot & Dry or Hot & Wet?
 Sweating
stops usually from destruction of
sweat glands or due to dysfunction from sensory
overload
 Patient
may still be covered with sweat though
from earlier exertion (i.e.: marathoner,
construction worker)
 Classic
heatstroke – hot, red, dry skin
 Exertional
heatstroke– hot, moist skin
28
Classic vs Exertional Heatstroke


Predisposing factors for classic heatstroke

Age

Diabetes

Other medical conditions
Predisposing factors for exertional heatstroke

Generally person in good health

Excessive ambient temperature with excessive
exertion with prolonged exposure and poor
acclimation
29
Exertional Heatstroke – Big Problems
 Severe
 From
metabolic acidosis
excessive lactic acid accumulation
 Lactic
acid develops as by-product during
anaerobic metabolism
 Hyperkalemia
– excessive potassium moved
from the cell into the bloodstream
 Released
from injured cells or created due
to renal failure (poor clearing capability) or
development of metabolic acidosis
30
Signs and Symptoms Heatstroke

Hot skin that is dry or moist

Very high core temperature

Deep respirations (blowing off acids) that become
shallow, rapid and later slow

Rapid, full pulse initially then slow

Hypotension with low or absent diastolic

Confusion or disorientation or unconsciousness

CNS impairment – headache, anxiety, impaired
judgment, paresthesia, psychosis

Possible seizures
31
Treatment Heat Stroke

Move patient to cool environment

Remove unnecessary clothing

Fluid challenge
 Adult
 Peds

200 ml increments (formula 20 ml/kg)
20ml/kg to a max of 60 ml/kg
Rapid cooling procedures
 Douse
 Fan
towels or sheets with water and place over patient
body – increases air current flow (convection)
 Cold
packs to lateral chest wall, groin, axilla, neck,
temples, behind knees
32
Shivering

Shivering raises body core temperature
 Can

occur in the setting of too rapid of a cooling process
To stop shivering
 Adult:
 Can
 Peds:
 Total
repeat same dose in 2 minutes titrated to the max
Valium 0.2 mg/kg over 2 minutes
 Can
 Total
Valium 5 mg IVP/IO over 2 minutes
repeat same dose in 15 minutes titrated to the max
maximum is 10 mg for the adult
max for peds is 5 mg (<5 years old) and
10mg (>5 y/o)
33
Water Emergencies

Drowning
 Respiratory
impairment from submersion or
immersion in a liquid

Outcome
 Mortality
– death
 Morbidity
– developing a medical problem
 No
morbidity – no problem

A leading cause of death in children

Most drownings occur in freshwater – the
swimming pool
34
Sequence of Events of Drowning

Submersion

Struggle with attempt at breath holding

Instinctive inspiratory and swallowing efforts made
 Water
enters mouth, posterior oropharynx, and stomach

Apnea causes rise in retained CO2 levels; decrease in O2

Hypoxia stimulates trigger to gasp

Acidosis is developing

Reflexive laryngospasm and bronchospasm occur
 Minimizes
amount of water actually measured in lungs
35
Sequence cont’d

Reflex swallowing continues
 Gastric
distension,  for vomiting and aspiration

Hypotension, bradycardia then death occur

Water enters lungs (before laryngospasm or after
laryngeal relaxation)

Water in airways blocks gas exchange in alveoli

Even small amount of water washes away
surfactant
 Atelectasis
develops (alveolar collapse)
36
Surfactant

A thin film substance in alveoli that keeps
them open

Decreases pressure needed for subsequent
inflation

Without adequate levels of surfactant,
alveoli collapse
 Blood
shunted past collapsed alveoli and is not
oxygenated before it is perfused throughout the body
37
Drowning

Outcome determined by degree of anoxia

Goal of therapy directed at reversing anoxia

Prehospital interventions and treatment is the
same regardless of the source of the drowning –
freshwater versus saltwater
38
Factors Affecting Survival

Cleanliness of water source

Length of time submerged

Age of victim

General health status of victim

Positive influence on outcome – immediate
recognition of the drowning and initiation of
immediate CPR
39
Treatment Near Drowning

Routine medical care

Spinal precautions

Consider CPAP in the adult if indicated

If stable (awake, alert, warm and dry, B/P >90 in
adult, then transport
40
Treatment Near Drowning cont’d

Anticipate need for ventilation support

Anticipate vomitus and laryngospasms
 Suction

available for vomitus
Positive pressure ventilations (i.e.: BVM) for
laryngospasms
 Many
drowning victims may have foaming present
 Focus
on oxygenation and ventilation more than on
suctioning

Protect the patient from heat loss
 Remove
wet clothing, cover body as much as possible
41
Treatment Unstable Near Drowning
Altered Mental Status; B/P <90

Secure airway

Assess for hypothermia

 If
normothermic, treat dysrhythmias per protocol
 If
hypothermic, also follow hypothermic protocol
Assist ventilations as indicated
 BVM
1
– 1 breath every 5 – 6 seconds
breath every 3-5 seconds infant and child to 8
 Advanced
1
airway
breath ever 6 -8 seconds
42
Immune System

Responsible for fighting infection

The principle system involved in allergic reactions
 Goal-
rid body of offending foreign material (antigen)

Components found in blood, bone marrow, and
lymphatic system

Additional systems affected in immune response
 Cardiovascular
 Respiratory
 Nervous
 Gastrointestinal
43
Immune Response

To destroy or inactivate pathogens, abnormal cells,
or foreign molecules

Activation of cascade of events triggered by
exposure to foreign substance – an antigen

Immune system directs attack on foreign substance
to deactivate or destroy offending agent

There is a chemical attack of antibodies on the
invading agent or antigen
44
Immune Response cont’d

Primary response
 Initial
(first time) exposure to an antigen
 Antibodies
developed to respond at subsequent
exposures

Secondary response
 Release
of antibodies, upon recognition of the
antigen, to facilitate removal of offending antigen
45
Histamine

Potent chemical

Principle chemical released in allergic reaction

Goal of histamine release
 Minimize
body’s exposure to the antigen

Bronchoconstriction -  lung exposure

Increased intestinal motility - move antigen thru system

Vasodilation - remove antigen from circulation

Increased vascular permeability - remove antigen from
circulation
46
Histamine Release – Smooth Muscle
Constriction

Bronchoconstriction
 Minimizes
amount of antigen that can enter the
respiratory tract

Abdominal cramping
 From

increased gastric motility
Diarrhea and vomiting

Attempt to move antigen quickly through the
system and eliminate it from the body
47
Histamine Release – Increased Capillary
Permeability

Third spacing – fluids (plasma) shift from intravascular to
interstitial space
 Trying

to move offending antigen out of circulatory system
Angioedema especially of head, neck, face, upper airway

Relative hypovolemia

Decreased cardiac output

Decreased tissue perfusion

Impaired cellular function

Cellular death
48
Histamine Release – Peripheral
Vasodilation

Decreased peripheral vascular resistance

Less tone in blood vessels

Less efficient circulation of blood

Decreased preload – amount of blood returning to
the heart

Decreased after-load – the pressure the heart must
pump against to move blood
 Blood

pressure will drop
Cardiac output drops
49
Allergic Reaction

Exaggerated response by immune system to foreign
substance (antigen)

Repeated exposure results in much stronger immune
response

Hypersensitivity
 Unexpected,

exaggerated reaction to an antigen
Range from mild skin rashes to more severe systemic
reactions throughout many more body systems
50
Anaphylaxis

Most severe allergic reaction

Usually occurs when an antigen enters the circulation
 Rapid
and wide distribution facilitated through-out the
body

Most reactions occur within seconds
 In

a few cases there may be a delay over an hour
The more severe the reaction, the quicker the onset of
signs and symptoms
51
Anaphylaxis

Life-threatening emergency requiring prompt
recognition and intervention

Can develop in seconds; can cause death in
minutes after exposure

Develops after exposure and sets off biochemical
reactions that could lead to shock and death

Most common causative agents – injected
penicillin and hymenoptera (bee and wasp) stings
52
Anaphylaxis – Presentation / Appearance

Flushing

Rash – fine, red, diffusely spread over entire body

Itching

Hives (urticaria) – wheal of red, raised bumps
across body

Swelling – 3rd space fluid shift

Pallor and/or cyanosis
53
Anaphylaxis – Respiratory System
 Respiratory
 Sneezing,
difficulty with tachypnea
coughing – trying to rid offending
antigen
 Wheezing,
 Laryngeal
stridor – bronchoconstriction & edema
edema – 3rd space fluid shift
 Laryngospasm
– may cause difficulty in being
able to speak
 Bronchospasm
 Labored
breathing; use of accessory muscles
54
Anaphylaxis – Cardiovascular System

Vasodilation

Increased heart rate – compensation attempt

Decreased blood pressure – from capillary leakage,
peripheral vasodilation and eventual failure of
compensatory mechanisms

Development of acidotic and hypoxic environment

Eventual fall in cardiac output
55
Anaphylaxis – Nervous System

Dizziness

Headache

Change in level of consciousness

Convulsions

Tearing
56
Anaphylaxis – Gastrointestinal System

Nausea and vomiting – to rid offending antigen

Abdominal cramping – hypermotility

Diarrhea – to rid offending antigen
57
Anaphylaxis – Ominous Signs

Decline in respiratory rate
 Following
increasing edema of tissues and initial
dyspnea

Bradycardia
 After

compensatory mechanisms have failed
Drop in blood pressure
 Significant
3rd space fluid shift has occurred along
with peripheral vasodilation
58
Allergic Reactions

Less severe immune response

Gradual onset of signs and symptoms

Milder signs and symptoms

Normal mentation

Adequate perfusion status of the patient

Response could be localized to one particular area
 Ex:
Forearm site for localized reaction to bee sting
59
Allergic Reactions

May experience mild flushing, itching, and rash

Urticaria (hives) may be present

May experience mild bronchoconstriction
 Body

still trying to minimize exposure to antigen
Mild abdominal cramps and diarrhea
 Body
still trying to rid self of offending antigen
60
Intervention of Allergic Reactions

To know the correct intervention relies on an
accurate and detailed assessment

Goals
 Determine
 Allergic
extent of immune response
reaction or anaphylaxis
61
Interventions

Epinephrine
 Vasoconstrictor
 Bronchodilator

Benadryl
 Antihistamine-
stop release of
histamine response

Fluids
 Volume
expansion
62
Region X SOP - Allergic Reaction Stable

Hives, itching, red skin

GI distress

Alert, warm and dry; systolic B/P >90mmHg

Ice pack to site

Benadryl (antihistamine) 25 mg IVP slowly over 2
minutes or IM
 Peds
Benadryl 1 mg/kg IVP to adult max of 25 mg
63
Region X SOP – Allergic Reaction Stable
with Airway Involvement

Epinephrine 1:1000 0.3mg SQ
 May
 Peds

dose Epi 1:1000 0.01 mg/kg SQ (max 0.3 mg)
Benadryl 50 mg IVP slowly over 2 minutes or IM
 Peds

repeat in 5 minutes
dose Benadryl 1 mg/kg (max 50 mg)
If wheezing
 Duoneb
treatment
 Albuterol
 If
2.5 mg with Atrovent 0.5mg
no improvement repeat Duoneb treatment
64
 If
no improvement, albuterol alone
Region X SOP – Anaphylactic Shock

Altered level of consciousness

Systolic B/P <90 mmHg

Secure airway
 Make
sure patient can ventilate/breathe and is
adequately oxygenated

Goals of treatment

Open airways

Support vascular status
65
Adult Anaphylactic Shock Medications

Epinephrine 1:1000 0.5 mg IM
 Can
repeat in 5 minutes

Benadryl 50 mg IVP/IO slowly over 2 minutes or IM

IV/IO fluid challenge in 200 ml increments

Duoneb treatment – Albuterol with Atrovent
 If
no improvement, administer Albuterol alone every 5
minutes
66
Pediatric Anaphylactic Shock Medications

Epinephrine 1:1000 0.01 mg/kg IM
 Max
0.3 mg/0.3 ml per single dose
 May
repeat in 5 minutes

Benadryl 1 mg/kg to max of 50 mg

Fluid challenge 20 ml/kg
 Titrated
 Max

to desired patient response
60 ml/kg
Duoneb treatment – Albuterol with Atrovent
 If
no improvement, administer Albuterol alone every 5 minutes
67
Continued Deterioration Anaphylaxis
 Contact
Medical Control to consider
 Epinephrine
 Adult
 Peds
1:10,000 0.5 mg IVP/IO
1:10,000 0.01 mg/kg IVP/IO
 Administer
 This
A
1:10,000
slowly
is adrenaline
strong cardiac stimulant!!!
 Have
patient on the cardiac monitor
68
Epi Pens

Prescribed medication for use by patients

Adult dose (yellow) – 0.3 mg

Peds dose (green) – 0.15 mg

To activate

Cap removed

Gripped firmly – keeping fingers away from tip

Jabbed into outer thigh and held in place 10 seconds

Caution – needle remains exposed after activation

Note: If patient’s EpiPen is ready to be used by them, don’t
delay. Assist patient in using their pen; repeated doses, if
necessary, of Epinephrine will be your stock
69
Pacemakers

Artificial pulse generator that delivers
an electrical current
 Stimulates
depolarization

Useful when normal pacemaker site
(SA node) unreliable

How would you know a patient has one?

Patient tells you

See it written in the history

See the bulge under the skin

Medic alert tag
70
Pacemaker Components

Power source
 Battery

unit called pulse generator
Conducting wire
 Electrodes

from the battery to the heart
Return wire
 Wire
that returns to the battery unit to complete
the electrical circuit
71
Pacemaker Types - Temporary

Usually used in acute setting and for relatively
short periods of time (i.e.: acute MI)

Pacing unit outside the body
 Transcutaneous
 Transvenous

– stimulus across the skin
– via venous vessel access
Current measured in milliamperes (mA)
72
Pacemaker Type - Permanent

Long term support anticipated

Wires inserted surgically into the right heart

Battery implanted in fatty layer pocket
under the skin of the chest or abdominal wall
 May
be inferior to right or left clavicle
 Usually
opposite side to dominant hand
 Could
be abdominal placement – rarer nowadays
 Could
be combination with AICD
 Current
AICD’s also have capability to pace
73
Pacemaker Sensing

Parameters set on pacemaker determine if pacing
stimulus is necessary or is withheld
 Demand
mode – pacemaker functions only when
patient’s own rate falls below a preset value
 Pacemaker
 Most
functions on “demand”
common type of pacemaker setting used
 Fixed
mode – pacemaker will fire regardless of
what the intrinsic (normal) conduction system does
 Infrequently
seen nowadays
74
Pacemaker Types - Ventricular

Single-chamber pacemaker

Stimulates only the ventricles

See spike followed by wide QRS

Most common type of pacemaker implanted

Can look like slow monomorphic VT at first glance
 But,
spikes are present; history supports pacemaker
75
Pacemaker Type - Atrial

Single chamber pacemaker

Atria are depolarized

Heart’s own conduction system used to stimulate the
ventricles

See spike followed by P wave and then normal QRS
76
Pacemaker Type – AV Synchronous
 Dual-chamber
 Both
pacemaker
atria and ventricles are stimulated
 Atrial
kick is restored
 Atria
contract and therefore squeeze more
blood to the ventricles prior to each
contraction
 See
spike followed by P wave and then
spike followed by wide QRS
77
Pacemaker
Malfunction –
Failure to Capture
 Spike
not followed
by complex therefore no depolarization
 Causes:
Battery failure, displacement of lead wire,
energy (mA) too low, edema/scar tissue or perforation
of myocardium, electrolyte imbalance
 Presentation:
fatigue, bradycardia, low B/P, syncope
78
Failure to Capture EMS Intervention

EMS intervention: reposition patient in case of loss of
lead wire contact – turn patient onto left side
 May

“float” lead wire into myocardial wall contact
Follow symptomatic bradycardia protocol
 Administer Atropine
 Apply
0.5 mg IVP
and prepare to begin operation of TCP
79
Pacemaker Malfunction – Failure to
Sense / Competition

Pacemaker fires regardless of the patient’s own rhythm

No sensing of spontaneous myocardial depolarization

There is potential competition for control of the heart

Danger – pacemaker spike may fall on vulnerable
downslope of T wave VF

Causes
 Battery
failure, fracture of wire,
displacement of electrode tip
80
Pacemaker Malfunction – Runaway Pacemaker

Pacemaker rate too fast but continues to capture

Malfunction of impulse generator
 Not

as common in newer models of pacemakers
Typical pacemaker rate set around 70’s (beats per
minute)
81
Pacemaker Malfunction – Battery Failure

Absence of any spikes when they would be
anticipated

Can cause life-threatening situation where
patient dependent on pacemaker to support a
healthy heart rate

Close patient monitoring and long battery life
usually avoids this problem
82
Assessment of Patient

Always check the patient first

Determine perfusion status / mechanical response
 Evaluate
the patient’s level of consciousness
 Evaluate
blood pressure to determine perfusion
 Presence

of radial pulse indicates B/P is present
EKG strip is printable representation of electrical
activity
83
Assessment of Paced Rhythm

Does each spike capture?
 Each
spike is followed by a complex

Is rate reasonable?

Are spikes competing with the patient’s rhythm?

Is pacemaker functioning consistently and
reliably?
84
Patient Management

If pacemaker malfunctions, treat the
patient and not necessarily their rhythm
 Don’t
treat the pacemaker

Provide a copy of the rhythm strip for
documentation in the patient’s hospital medical
record

It is safe to touch a patient if the TCP is in use
 Electrical
stimuli is not transferred to you
85
Transcutaneous Pacing – Potential
Complications

Coughing

Skin burns

Interference with sensing from patient agitation
or muscle contractions

Pain

Failure to recognize non-capture

Tissue damage
 3rd
degree burns
86
Documentation of TCP Use

Initial and repeat EKG rhythms on patient chart

Date and time pacing started
 Rate
 Output
(mA) to obtain capture
 Patient’s

response
Intervention for comfort/pain control measures
 Valium
A
2 mg IVP/IO; repeated to max of 10mg
benzodiazepine to take the edge off
 Fentanyl
A
1 mcg/kg IVP/IO/IN; repeated in 5 minutes
synthetic opioid for pain control
87
QuickTrach

Indications
 Emergency
assisted ventilations when all other means
have failed

Contraindications
 Tracheal
transection; other measures are successful

Adult device – size 4.0 mmID if >77# (>35 kg)

Peds device – 2.0 mmID if 22-77# (10-35 kg)
 <22#
(10 kg) – use needle cricothyrotomy procedure
88
Quick Trach Procedure

Attempt to ventilate patient

Assemble equipment
 Quick
Trach kit – appropriate size
 BVM
 Skin
prep material
 4x4’s

Position patient supine, neck hyperextended if able
89
Quick Trach Procedure cont’d

Locate Cricothyroid membrane
 Inferior
to thyroid cartilage (Adam’s apple)
 Superior
 Palpate

to cricoid cartilage
from notch upward
 1st
bone is cricoid cartilage
 Go
to space just above this bone
Cleanse site
90
Quick Trach Procedure cont’d

Secure larynx laterally between thumb
and forefinger
 Anchor
and stretch skin slightly

Puncture Cricothyroid membrane at 900 angle

Confirm entry of needle to trachea
 Aspirate

air through the syringe
Change angle of insertion to 600 with tip pointed
toward feet
91
Quick Trach Procedure cont’d

Advance device to level of red stopper
 Red
stopper assures proper initial depth insertion
 Stopper
should now be snug against the skin

Remove the stopper

Hold needle and syringe firmly
 Slide
only plastic cannula forward until hub of
cannula snug against skin as you withdraw the needle
 Note:
Similar maneuver when starting an IV and
advancing the catheter as you retract the stylet
92
Quick Trach Procedure cont’d

Distal end of flexible tubing attached to Quick Trach
hub

BVM attached to proximal end of flexible tubing
 Helpful
to have flexible tubing already attached to BVM

Immediately begin to ventilate with 100% O2

Use pre-attached strap to secure device
 Make
sure device is snug against skin
 Device
can easily be coughed out
 Helpful
to have one end of strap already attached to
device prior to insertion
93
Quick Trach Use

Confirm placement by auscultation and
observation of chest rise

Continuously monitor airway and lung
sounds to ensure proper placement

Monitor for over expansion of chest wall
 May
need to detach BVM to allow for passive
exhalation to allow deflation of lungs

Note general improvement in patient’s overall
condition
94
Case Scenario Discussion

Review presentation of patient

Determine your general impression

Determine your treatment choice
 Use
your SOP booklets as a resource

Discuss reassessment steps

Discuss documentation highlights related to the
patient situation
95
Case Scenario #1

Patient works on a road crew

Complains of feeling lightheaded and dizzy

VS: 148/88; P – 90; R – 20; warm and sweaty

History: hypertension, high cholesterol, diabetes

General impression?

Interventions?
96
Case Scenario #1


General impression
 Heat emergency (exhaustion)
 Consider
diabetic problem (blood sugar 72)
 Consider
other medical problems
Intervention
 Remember
to consider other causes of feeling
lightheaded and dizzy
 Cool
– remove from heat, remove extra clothing
 Fluids
– 200 ml fluid bolus increments
97
Case Scenario #2

Person training for a marathon found collapsed on
a trail; unknown length of time
 Temperature
outside 940 and 85% relative humidity

Unknown medical history

Patient moans when touched

Hot and moist

VS: 86/62; P – 110; R – 28 and labored

General impression?

Interventions?
98
Case Scenario #2

General impression
 Heat stroke
 Acute
medical problem – acute MI, brain insult
 Trauma

Interventions
 Begin
 IV
to cool – wet towels, fanning, air conditioning
– O2 - monitor
 IV
fluids – 200 ml incremental fluid challenges
 Remember
to consider other causes of altered level of
consciousness
99
Case Scenario #3

Your adult patient was drinking from a can of soda
and was stung by a bee that was in the can

Has swollen lips

Complains of itchy throat and a feeling of swelling
in the throat

VS: 110/70; P – 98; R – 22; SpO2 97%

General impression?

Interventions?
100
Case Scenario #3

General impression
 Allergic reaction with airway involvement

Interventions
 Consider
IV – O2 - monitor
 Epinephrine
 May
repeat every 5 minutes
 Benadryl
 If
1:1000 0.3 mg SQ
50 mg slow IVP or IM
wheezing, Duoneb ( may repeat)
101
Case Scenario #4

Adult patient ate a dip and 15 minutes later
complains of abdominal cramping, diarrhea, all
over itching

You can hear audible wheezing
 Confirmed
bilateral wheezing – breath sounds
barely audible

VS: B/P 88/60; P – 116; R – 22

General impression?

Interventions?
102
Case Scenario #4

General impression
 Anaphylactic shock
 Interventions
 IV
– O2 – monitor
 Epinephrine
1:1000 0.5 mg IM (may repeat every 5
minutes)
 Benadryl
 Fluid
 Duo
50 mg IVP/IO or IM
challenge – 200 ml increments
neb (may repeat Albuterol neb if needed)
103
Case Scenario #5

Your 78 year old patient complains of pounding in
their chest and generally not feeling well

Pulse is irregular, skin warm and moist

VS: B/P 92/50; P – 40; R – 18; SpO2 97%

Hx: Hypertension, gout, CABG, pacemaker, high
cholesterol

General impression?

Interventions?
104
Case Scenario #5

General impression
 Consider

cardiac problem
Intervention
 Apply
cardiac monitor
 Consider
obtaining 12 lead EKG, if possible, on cardiac calls
105
Case Scenario #5

Impression – Pacemaker with failure to capture

Intervention
 Turn
patient onto their left side
 May
“float” catheter into position
 Support
perfusion
 Consider Atropine
 Prepare
dose
for application TCP
 Consider
need for Dopamine drip to support blood pressure
 Increases
strength of cardiac contractions
106
Bibliography
 Bledsoe, B., Porter, R., Cherry, R. Paramedic Care Principles &
Practices, 4th edition. Brady. 2013.
 Region X SOP’s; IDPH Approved April 10, 2014.

Mistovich, J., Karren, K. Prehospital Emergency Care 9th
Edition. Brady. 2010.

http://www.scientificamerican.com/article/why-does-lacticacid-buil/

http://www.icufaqs.org/Pacemakers.doc

http://www.cdc.gov/HAI/organisms/cdiff/Cdiff_infect.html

http://www.cdc.gov/norovirus/preventing-infection.html
107
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