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PRE-HOSPITAL
MEDICAL
Guidelines
Christopher M Eberlein, MD
Medical Director
Gundersen Health System
cmeberle@gundersenhealth.org
01-18-2016
CONTENTS
Contents ..................................................................................................................................................................................................2
FOREWARD .........................................................................................................................................................................................5
FORWARD CONTINUED .................................................................................................................................................................6
General Principles of Patient Care ............................................................................................................................................8
General Principles of Patient Care Continue .......................................................................................................................9
Abnormal Delivery .........................................................................................................................................................................10
Air Ambulance Use .........................................................................................................................................................................11
Airway Management .....................................................................................................................................................................12
Airway Obstruction........................................................................................................................................................................13
Altered Mental Status ...................................................................................................................................................................14
Amputation ........................................................................................................................................................................................15
Anaphylaxis/Allergic Reaction ................................................................................................................................................16
Automatic Implantable Cardiac Defibrillator (AICD) Deactivation ......................................................................17
Asthma / COPD ................................................................................................................................................................................18
Asystole ................................................................................................................................................................................................19
Bradycardia........................................................................................................................................................................................20
Blood Pressure Management ....................................................................................................................................................21
Burns .....................................................................................................................................................................................................22
Cancellation of Call .........................................................................................................................................................................23
Cerebrovascular Accident (Benchmark) ............................................................................................................................24
Stroke Benchmarks ........................................................................................................................................................................25
Coronary Insufficiency (Benchmark) ...................................................................................................................................26
STEMI Benchmark Check List ..................................................................................................................................................27
Continuous Positive Airway Pressure..................................................................................................................................28
Crush Syndrome ..............................................................................................................................................................................29
Decompression Sickness .............................................................................................................................................................30
Determination of Death ...............................................................................................................................................................31
Diabetic Emergency .......................................................................................................................................................................32
Emergency Childbirth...................................................................................................................................................................33
Envenomation ..................................................................................................................................................................................34
EZ-IO ......................................................................................................................................................................................................35
General Medical ...............................................................................................................................................................................36
General Trauma ...............................................................................................................................................................................37
Head Injury ........................................................................................................................................................................................38
Heat Related Illness .......................................................................................................................................................................39
Hemostatic Agent Use...................................................................................................................................................................40
Hyperkalemia....................................................................................................................................................................................41
Hypothermia .....................................................................................................................................................................................42
Inter-facility Pre-Transport Care............................................................................................................................................43
IFT of Insulin ....................................................................................................................................................................................44
IFT of Pantoprazole (Protonix) Or other PPI ...................................................................................................................45
IFT of tPA (tissue plasminogen activator) .........................................................................................................................46
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FOREWARD
01-18-2016
FORWARD CONTINUED
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01-18-2016
Universal precautions and personal protective equipment shall be utilized at all times as is
appropriate for the situation.
o PPE can include but is not limited to:
Fluid barrier gloves
Safety eye protection
Infection control gown
Infection control shoe covers
Infection control bouffant cap
Surgical mask
N-95 mask
All patients shall receive a primary assessment to include, but not limited to the following:
o Airway patency
o Breathing (rate and quality)
o Circulation
Pulse
Skin color, temp, and condition
Assess for and treat life threatening bleeding
o Level of consciousness
All patients shall receive a secondary assessment to include, but not limited to the
following:
o Vital signs including but not limited to:
Pulse
Blood Pressure
SpO2
Respiratory rate and effort
o S.A.M.P.L.E. history as possible
o Rapid trauma and/or focused physical assessment
o Secondary head-to-toe physical assessment
01-18-2016
All Primary and initial Secondary assessments shall be performed or supervised by the EMS
provider with the most advanced level of training nationally recognized.
All patients shall receive treatment as is appropriate per protocol and on-line medical
direction.
All patients shall be re-assessed after an intervention is performed. The success, secondary
effects, and possible side-effect of said intervention evaluated.
o i.e. if a protocol gives a medication dose such as Fentanyl 25-100 mcg Q 5 minutes;
the care provider shall give the initial appropriate dose of 25-100 mcg and perform
a re-assessment of the patient to include pain level, level of consciousness, and vital
signs prior to giving a second dose.
o The same principle applies to the titration of a medication. Titration is the
adjustment of medication dosing until the desired endpoint is reached. The
endpoint is the point at which the titration is complete as determined by an
indicator.
o i.e. titration of a Nitroglycerin drip to achieve a blood pressure of 185 systolic:
SBP of 185 mmHg is the endpoint
Starting dose if given per protocol
The care provider shall initiate the NTG drip per protocol.
The care provider shall assess vital signs.
The care provider shall adjust NTG drip per protocol.
The care provider shall assess vital signs.
This shall be repeated until the desired endpoint is reached or
patient care is transferred.
For pediatric patients:
o Equipment and medications must be appropriate for the size and weight of the
patient. Use of the Broselow Tape or equivalent is encouraged.
o The developmental age of the infant/child must be considered in the
communication and evaluation for treatment.
o Treatment priorities are similar to the adult patient.
o When appropriate, family members should remain with pediatric patients.
o Infants and children must be properly restrained prior to and during transport.
If a hospital declares an Internal Disaster or informs EMS agencies that they are on
diversion, that facility is to be bypassed for ALL patients except medical patients in cardiac
arrest or in whom the ability to adequately ventilate has not been established.
Patients will be transported to the closest appropriate facility per local, state, and federal
laws and guidelines.
o If two hospitals are of similar distance and have similar capabilities/resources for
the patients nature of illness, mechanism of injury, or clinical impression, the
patient will be transported to the hospital of their preference.
If the patient has no preference, the patient will be transported to the hospital
providing on-line medical direction at that time.
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ABNORMAL DELIVERY
General Scope: Protocol for delivering infants presenting with ominous signs.
Applies to: All Medical Staff
Protocol:
1. Perform routine medical assessment
2. If Meconium staining is present:
a. Tracheal suctioning via ETT prior to stimulation and ventilation
b. See Neonatal Resuscitation Protocol
3. If prolapsed cord is present:
a. Do not push cord back in, cover with sterile towel moistened with warm NS
b. Place mother in Trendelenburg knee to chest position
c. With gloved hand, push presenting part off cervix to decompress cord and maintain
position en route to hospital
4. If infant is breech:
a. Deliver baby to waist
b. Rotate to face down position (The head should deliver on its own within 3 minutes)
c. Create breathing space around babys face with gloved hand (middle and index
finger along the baby's face and up to its nose)
d. Suprapubic pressure may help keep the head flexed and facilitate delivery
e. Try to assist delivery by placing finger in babys mouth and gently pulling
5. If other part is presenting (arm, foot, etc):
a. Do not pull on part
b. Cover exposed part with sterile towel moistened with warm NS
c. Place mother left side down
6. Multiple births:
a. After initial delivery, tie and cut cord
b. Proceed with subsequent deliveries
7. Rapid transport
8. Update Medical Control
APGAR SCORING:
Sign
Pulse
Respirations
Muscle Tone
Reflex irritability
Color
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0
Absent
Absent
Limp
None
Pale or Blue
1
<100
Slow or Irregular
Some flexion
Grimace
Pink body/blue
extremities
2
>100
Good Crying
Active motion
Cough or sneeze
Completely pink
1.
2.
3.
1.
1.
falls
01-18-2016
b.
c.
d.
children
a. should be triaged preferentially to pediatric
deterioration
4.
a.
3.
3.
2.
pelvic fractures
a.
b.
paralysis
Me cha ni s m of I nj ur y
2.
c.
years
2.
3.
4.
5.
6.
7.
8.
older adults
a.
b.
b.
5.
6.
AIRWAY MANAGEMENT
General Scope: Protocol for airway management
Applies to: All Medical Staff
Protocol:
1. Perform routine medical assessment
a. Consider EtCO2 monitoring if appropriate for scope of practice
2. If patient has a history of COPD
a. Titrate SpO2 to 90-92%
i. If respiratory rate<30 titrate SpO2 with nasal cannula
ii. If respiratory rate>30 apply partial rebreather mask, goal of 100% SpO2
b. Use the least amount of supplemental oxygen as necessary
3. If patient does not have history of COPD
a. Titrate SpO2 to >94%
i. If respiratory rate<30 titrate SpO2 with nasal cannula
ii. If respiratory rate>30 or SpO2<94% apply partial rebreather mask
b. Use the least amount of supplemental oxygen as necessary
4. If patient presents with bronchospasm
a. See Asthma / COPD Protocol
5. For respiratory failure despite above
a. Consider CPAP
b. See CPAP Protocol
6. For respiratory failure despite above
a. See Respiratory Failure Protocol
Note:
Signs of impending respiratory failure include:
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AIRWAY OBSTRUCTION
General Scope: Protocol for airway obstruction.
Applies to: All Medical Staff
Protocol:
1. Perform routine medical assessment
2. If patient is unable to speak and is conscious
a. Perform Heimlich maneuver until the foreign body is expelled or the victim becomes
unconscious
3. If patient is unable to speak and is unconscious
a. Perform tongue-jaw lift
b. Use finger sweep if object is visible
c. Attempt ventilation
d. If obstruction persists, reposition and re-attempt ventilation
e. Give up to five chest thrusts
f. If obstruction persists perform CPR per ECC 2010 guidelines
i. Repeat steps a-f until obstruction is dislodged or 5 cycles
4. [EMT-B, EMT-I, AEMT, Paramedic] If unable to ventilate attempt direct laryngoscopy and
removal with Magill forceps
5. [Paramedic / Med Control] If unsuccessful in removing foreign body or relieving upper
airway obstruction see Surgical Cricothyroidotomy Protocol
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01-18-2016
AMPUTATION
General Scope: Protocol for treatment of patients who have experienced an amputation
Applies to: All Medical Staff
Protocol:
1. Perform routine trauma assessment
2. Consider tourniquet for uncontrolled bleeding
3. Consider activation of air ambulance for transport to medical center specializing in reimplantation
4. [EMT-I/AEMT] Establish IV/IO per Vascular Access Protocol
5. See Trauma Care Protocol
6. See Pain Management Protocol
7. Irrigate amputated part with NS to remove gross contaminants (do not debride)
8. Place amputated part in sterile gauze moistened in NS
9. Place amputated part in sterile waterproof container
10. Place sealed container in iced NS or place activated cold packs around container
01-18-2016
ANAPHYLAXIS/ALLERGIC REACTION
General Scope: Protocol for treatment of patients who present severe allergic reaction
Applies to: All Medical Staff ** (optional use by EMR/ EMT/ AEMT service and then only with approval
of medical director, documentation of additional training, and prior approval of the Operational Plan by
the State EMS office)
Protocol:
1. Perform routine medical assessment
a. Remove offending agent
2. Airway support as needed, see Airway Management Protocol
3. If signs/symptoms of anaphylaxis:
a. EPINEPHERINE (use with caution in elderly/patients with coronary artery disease)
i. [**EMR/EMT] Epi-pen or Epi-pen Jr. if available
ii. [EMT/Paramedic] **0.3mg (1:1000) IM {child <8y/o 0.15mg}
iii. [Paramedic] 0.1-0.5mg (1:10,000) IV over 5 minutes {child 0.01mg/kg}
4. If localized reaction
a. Ice and elevate affected area as practical
b. [Paramedic]Consider BENADRYL 25-50mg IV or 50mg IM {child 1.25mg/kg}
5. [EMT-I, AEMT, Paramedic] Establish IV/IO per Vascular Access Protocol but do not delay
administration of EPINEPHRINE
a. [Paramedic] BENADRYL 25-50mg IV or 50mg IM {child 1.25mg/kg}
b. [Paramedic] SOLUMEDROL 125mg IV
6. If SBP<90 see Blood Pressure Management Protocol
7. If bronchospasm is present:
a. ALBUTEROL via nebulizer
i. [EMT] 2.5mg
ii. [EMT, EMT-I, AEMT,Paramedic] Consider 5.0mg
iii. [Paramedic] Consider continuous neb (10-20mg)
Note:
Anaphylaxis = syndrome of severe hypersensitivity reaction characterized by cardiovascular collapse and
respiratory compromise.
1. Presentation:
a. Symptoms may begin within seconds or may be delayed up to one hour from
exposure
b. Generalized angioedema
c. Tightening sensation in throat and chest progressing to laryngeal and bronchial
spasm manifested by hoarseness, stridor and wheezing
d. Frequently see nausea, abdominal cramps, vomiting and diarrhea
e. Impending cardiovascular collapse presents with tachycardia and hypotension
f. Localized redness, swelling, and/or itching alone is NOT anaphylaxis
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ASTHMA / COPD
General Scope: Protocol for treatment of asthma and chronic obstructive pulmonary disease
Applies to: All Medical Staff
**(Duo-Neb optional for EMT-Basic Service and then only with approval
of medical director, documentation of additional training, and prior approval of the Operational Plan by
the State EMS office)
Protocol:
1. Perform routing medical assessment
2. Begin initial treatment per Airway Management Protocol
3. If mild attack (Slight increase in respiratory rate, mild wheezes, and good skin color)
a. Consider ALBUTEROL via nebulizer
i. [EMT] 2.5mg
ii. [EMT, EMT-I, AEMT, Paramedic] Consider 2.5-5.0mg
b. [EMT-I, AEMT, Paramedic] Consider IV NS TKO
4. If moderate attack (Marked increase in respiratory rate, wheezes easily heard, and
accessory muscle use)
a. Consider ALBUTEROL via nebulizer
i. 2.5mg
ii. [EMT, EMT-I, AEMT, Paramedic] Consider 2.5-5.0mg
b. [EMT-I, AEMT, Paramedic] Consider IV NS TKO
5. If severe attack (Respiratory rate more than twice normal, loud wheezes or silent chest,
patient anxious, and/or gray or ashen skin color)
a. ALBUTEROL via nebulizer
i. 2.5mg
ii. [EMT, EMT-I, AEMT, Paramedic] Consider 5.0mg
iii. [Paramedic] Continuous neb
b. [EMT-I, AEMT, Paramedic] Consider IV NS TKO
c. [EMT-B**, EMT-I, AEMT, Paramedic] DUO-NEB nebulizer treatment
d. [Paramedic/Med Control] SOLUMEDROL 125mg IV
i. Pediatric dosing 1 mg/kg
e. [Paramedic/Med Control] MAGNESIUM 2 grams IV over 15 minutes
f. [EMT-I, AEMT, Paramedic] EPINEPHRINE (1:1000) 0.01mg/kg IM if possible
allergy-induced asthma
i. Up to 0.3mg
g. If failure of above
i. See Rapid Sequence Intubation Protocol
01-18-2016
ASYSTOLE
General Scope: Protocol for treatment of a patient in asystolic cardiac arrest
Applies to: EMT-I/ Paramedic
Protocol:
1. Perform routine medical assessment
2. Initiate CPR and continue throughout resuscitation with minimal interruptions
3. Consider possible causes and treatments (Hs & Ts)
a. Hypoxia ventilation see Airway Management Protocol
b. Hypoglycemia check blood sugar
c. Hypothermia see Hypothermia Protocol
d. Hyperkalemia see Hyperkalemia Protocol
e. Hypovolemia consider 1000cc IV NS bolus see Vascular Access Protocol
f. (H+)Preexisting acidosis Ventilations, consider [Paramedic] SODIUM
BICARBONATE 1 amp IV
g. (Toxins)Drug overdose see Poisoning and Overdose Protocol
h. Tension pneumothorax consider [Paramedic] Needle Thoracentesis
i. Tamponade (Cardiac Tamponade)
j. Thrombosis PE/MI
4. Confirm asystole in two leads
a. If rhythm is unclear, see V-Fib/Pulseless V-Tach Protocol
5. Establish IV/IO per Vascular Access Protocol
6. Establish airway per Respiratory Failure Protocol
7. [Paramedic] Administer EPINEPHRINE (1:10,000) 1mg IV/IO Q 3-5 minutes
8. Update Medical Control
a. May request termination of efforts
01-18-2016
BRADYCARDIA
General Scope: Protocol for treatment of an adult patient with symptomatic bradycardia
Applies to: All Medical Staff
Protocol:
1. Perform routine medical assessment
2. Monitor SpO2
a. Airway support as needed per Airway Management Protocol
3. Identify patient as having serious signs or symptoms
a. [Basic EMT**]Obtain EKG. [EMT-I, Paramedic] review EKG if available
4. [EMT-I, AEMT, Paramedic] Establish IV/IO per Vascular Access Protocol
5. If patient is asymptomatic, observe closely
6. [Paramedic] If symptomatic 2nd or 3rd degree block or IV/IO not readily available
a. begin TRANSCUTANEOUS PACING
i. Consider Pain Management Protocol and/or Sedation Protocol as needed
b. [Paramedic] Administer ATROPINE 0.5mg IV/IO Q 3-5 minutes to a max of
0.04mg/kg (adult 3mg)
c. [Paramedic/Med Control] Consider DOPAMINE drip (200mg/250ml D5W
800mcg/ml) Initiate infusion at 5mcg/kg/min and titrate every 5 minutes by
increments of 1-5mcg/kg/min up to 20mcg/kg/min.
a.
[Paramedic/Med Control] Consider EPINEPHRINE drip (1mg/100ml D5W or
NS10mcg/ml) Initiate IV infusion at 0.01mcg/kg/min (2 mcg/min) and
titrate every 5 minutes by increments of 0.01mcg/kg/min (1 mcg/min) up to
0.1mcg/kg/min (10 mcg/min) maximum rate to achieve SBP>90
01-18-2016
01-18-2016
BURNS
General Scope: Protocol for treatment of patients who have experienced a burn
Applies to: All Medical Staff
Protocol:
1. Perform routine trauma assessment
2. Consider activation of air ambulance for transport to medical center with a specialized burn
center
3. Airway support as needed, see Airway Management Protocol
4. [EMT-I/AEMT/Paramedic] Establish IV/IO per Vascular Access Protocol
5. See Trauma Care Protocol
6. See Blood Pressure Management Protocol
7. See Pain Management Protocol (IV ONLY)
8. If burn is thermal in nature:
a. Stop the burning process without causing hypothermia
b. Remove clothing and jewelry (Do not pull away clothing that is stuck to burn)
c. [EMT-I/AEMT/Paramedic] If burn is >10% BSA and ETA to hospital >15 minutes, IV
NS 150ml/hr
d. [Paramedic] Consider early intubation if signs of airway burns is present
9. If burn is chemical in nature:
a. Remove agent as appropriate
b. Irrigate for at least 15 minutes with NS
i. Use 1000ml for eye irrigation
ii. Use continuous irrigation for alkali burns
10. If burn is electrical in nature (severe high voltage injury):
a. Once scene is safe, remove the patient from the source
b. See Cardiac Dysrhythmia Protocols as needed
c. [EMT-I/AEMT/Paramedic] IV NS/LR x 2 lines
i. Run one line with 500-1000ml IV bolus
ii. [Paramedic/Med Control] Second line with SODIUM BICARBINATE 50mEq
per liter, run at 500-1000ml/hr
11. Dress burned area with dry sterile dressings (if burn BSA <10% may consider use of sterile
NS dressing)
12. Consider use of burn sheet with additional clean, dry sheet and blanket to conserve body heat
13. DO NOT BREAK BLISTERS. DO NOT APPLY CREAMS, OINTMENTS OR ANTIDOTES TO
BURNS
14. Update Medical Control
01-18-2016
CANCELLATION OF CALL
General Scope: Procedure for cancelling ambulance while en route to a call.
Applies to: All Medical Staff
Protocol:
1. When EMS is activated but a request from first responders to cancel is made, dispatch will
ask responding crew to continue in a non-emergency fashion
a. Cancellation will be at the discretion of the TSA/TSAR shift supervisor with
consideration given to call circumstances, system status, and weather
2. TSA/TSAR Crew may cancel under the following conditions
a. No physical patient exists or patient has left the scene
b. The call or address has been determined to be false in nature
c. The patients personal physician is in attendance and determines the ambulance is
not needed
01-18-2016
01-18-2016
STROKE BENCHMARKS
Rate of stroke scale assessment for patients diagnosed with a
stroke
Rate of BGL assessment for patients diagnosed with a stroke
Rate of BP assessment every 10 minutes for patients diagnose
with a stroke
Scene time < 15 minutes for stroke alert patients
Rate of hospital contact for a stroke alert < 10 minutes from
patient side with documentation of notification
Response time of < 10 minutes 90th% for patients diagnosed
with stroke
Maintenance of 02 Sat per protocol
% of patients with a diagnosis of stroke with a priority 2 EMD
and response
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01-18-2016
01-18-2016
Applies to: All Medical Staff ** (optional for EMT-Basic/EMT-I/AEMT Service and then only with
approval of medical director, documentation of additional training, and prior approval of the
Operational Plan by the State EMS office)
Protocol:
1. Determine need (Clinical Indications):
2. Moderate to severe respiratory distress with signs and symptoms of pulmonary edema,
CHF, or COPD, refractory to initial interventions, and all of the following apply:
a. Awake and able to follow commands
b. Over 12 years old and is able to fit the CPAP mask
c. Has the ability to maintain an open airway
i. And exhibits two or more of the following:
1. A respiratory rate > 26 breaths per minute
2. SPO2 < 92% on high flow oxygen
3. Use of intercostal or accessory muscles during respirations
4. Wet lung sounds
3. [EMT-I/AEMT/Paramedic] Establish IV/IO per Vascular Access Protocol
4. Talk patient through procedure and cautiously sedate as needed, see Sedation Protocol
5. Start CPAP at 5-10mmHg or pre-set level
Note:
1. Indications
a. Acute pulmonary edema as a bridge device
b. Patients already on CPAP
c. Mild respiratory failure due to muscle fatigue
d. COPD
2. Exclusion criteria
a. Recurrent aspiration
b. Large volumes of secretions
c. Inability to protect the airway
d. Vomiting
e. Obstructed bowel
f. Upper airway obstruction
g. Uncooperative, confused or combative patient
h. Inability to tolerate a tight mask
i. Orofacial abnormalities which interfere with mask/face interface
j. Untreated pneumothor
01-18-2016
CRUSH SYNDROME
General Scope: Protocol for treatment of patients experiencing crush syndrome. Protocol must be
initiated prior to patient extrication. This protocol is also appropriate for suspension trauma.
Applies to: All Medical Staff
Protocol:
1. Perform routine medical and trauma assessment
2. Airway support as needed, see Airway Management Protocol
3. [EMT-I/AEMT/Paramedic] Establish IV/IO per Vascular Access Protocol (aggressive
volume replacement is essential prior to extrication if possible)
a. If SBP<90mmHg
i. [EMT-I/AEMT/Paramedic] IV NS 2-3L bolus
b. If SBP>90mmHg
i. [EMT-I/AEMT/Paramedic] IV NS 1500ml bolus
4. See Trauma Care Protocol
5. Evaluate for hypothermia, see Hypothermia Protocol
6. Apply direct pressure to control external bleeding
7. Consider using a tourniquet on affected limb before extrication if possible
a. Leave the tourniquet in place for the transport
b. If transport >20 minutes, slowly release the tourniquet
8. Early stabilization of all extremity fractures aids in controlling blood loss
9. [Paramedic/Med Control] Consider IV NS with SODIUM BICARBINATE 50mEq per liter at
500-1000ml/hr
10. See Pain Management Protocol
01-18-2016
DECOMPRESSION SICKNESS
General Scope: Protocol for treatment of patients with potential decompression sickness.
Applies to: All Medical StaffProtocol:
1. Perform routine medical and trauma assessment
2. Place patient on 100% O2 via tight fitting mask if spontaneously breathing, see Airway
Management Protocol
3. [EMT-I/AEMT/Parmedic] Establish IV/IO per Vascular Access Protocol
4. Evaluate for hypothermia, see Hypothermia Protocol
5. See Blood Pressure Management Protocol
6. See Pain Management Protocol
7. Transport to the nearest hyperbaric chamber (consider air transport). Medical Control
must call to ensure chamber is available and working and establish an accepting physician
a. Contact:
i. Divers Alert Network 919-694-8111, ask for diving emergencies
ii. Hennepin County Medical Center
1. 800-424-4262 ED Physician
2. 612-873-3132 ED
3. 612-873-7420 Hyperbaric Department
iii. St. Lukes, Milwaukee 414-649-6577
iv. University of IA, Iowa City
1. 319-356-7706 (8-5)
2. 319-356-2233 (after hours)
3. 319-356-8220 HBO Physician
8. Update Medical Control
Note:
Definition
1. Decompression illness occurs when the gas
dissolved in the body fluids separates from
those fluids to form bubbles.
2. In a rapid ascent, the pressure differential
between the body tissues and blood and
alveoli becomes great enough to cause
separation of nitrogen from the liquid phase
resulting in the formation of bubbles in the
tissues or blood.
A. Predisposing factors that increase the incidence of
decompression illness
1. Dehydration
2. Cold temperatures
3. Obesity
4. Exercise during the dive
5. Older individuals
6. Previous joint injury
7. Previous recent dives
8. Flying after recent dive
01-18-2016
B.
C.
D.
DETERMINATION OF DEATH
General Scope: Protocol for not initiating or discontinuing CPR
Applies to: All Medical Staff
Protocol:
1. CPR must be initiated unless the following conditions exist
a. DNR in the form of WI DNR wristband
b. Valid POLST form with DNR orders
c. Direct order from Medical Control Physician
d. Triple Zero (pulseless, apneic, and asystolic) with one of the following:
i. Decomposition
ii. Rigor mortis
iii. Dependent lividity
iv. Decapitation
v. MCI
vi. Traumatic death with prolonged extrication with no CPR
2. Update Medical Control
3. Ensure Coroner/Medical Examiner is notified
01-18-2016
DIABETIC EMERGENCY
General Scope: Protocol for treatment of patients who present with diabetic emergencies
and then only with approval of medical director, documentation of additional training, and prior
approval of the Operational Plan by the State EMS office)
Protocol:
1.
2.
3.
4.
01-18-2016
EMERGENCY CHILDBIRTH
General Scope: Protocol for delivering infants.
Applies to: All Medical Staff
Protocol:
1. Perform routine medical assessment
2. If ominous signs see Abnormal Delivery Protocol
3. If imminent delivery:
a. [EMT-I/AEMT/Paramedic] Establish IV/IO per Vascular Access Protocol
b. Place mother in knee to chest position and prepare delivery equipment
c. Have mother pant through contraction and relax between
d. As head crowns at perineum, apply slight pressure to prevent explosive delivery
e. As head emerges, check for cord around neck
i. If cord is around neck and cannot be slipped overhead, clamp x 2 and cut
immediately
f. As soon as nose and mouth emerge, suction immediately before first breath
g. If HR<100 see Neonatal Resuscitation Protocol
h. Put baby on mothers abdomen and prevent heat loss
i. Take APGAR scores at 1 and 5 minutes
j. Deliver placenta (Place the cord and the placenta in a sack or container to be brought
to receiving facility)
k. Massage uterus if bleeding is brisk after delivery of the placenta
l. If heavy bleeding present see Post-Partum Hemorrhage Protocol
4. Transport if placenta has delivered or >15 minutes have elapsed
5. Update Medical Control
APGAR SCORING:
Sign
Pulse
Respirations
Muscle Tone
Reflex irritability
Color
01-18-2016
0
Absent
Absent
Limp
None
Pale or Blue
1
<100
Slow or Irregular
Some flexion
Grimace
Pink body/blue
extremities
2
>100
Good Crying
Active motion
Cough or sneeze
Completely pink
ENVENOMATION
General Scope: Protocol for treatment of patients with potential envenomation.
Applies to: All Medical Staff
Protocol:
1.
2.
3.
4.
5.
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EZ-IO
General Scope: Procedure for EZ-IO placement. Applies to: EMT-Intermediate Tech / AEMT /
Paramedics (** EZ-IO is optional for AEMT/EMT-IV services and only with approval of the medical
director, documentation of training, and prior approval of the Operational Plan by the State EMS Office)
Protocol:
1. Determine need rule out contraindications
2. Locate insertion site and clean area with antiseptic wipe
a. Use EZ-IO AD (25 mm) if > 40 kg; EZ-IO LD (45 mm) for obese patients with excessive tissue
over the insertion site; EZ-IO PD (15 mm) for 3-39 kg
b. Tibia (pediatric and adult)
i. Two finger widths below the patella is the tibial tuberosity
ii. One finger width medial to the tibial tuberosity is the point of insertion
c. Humeral head (always use the LD needle for adults)
i. Keep arm adducted with patients palm on their umbilicus
ii. Place in the greater tubercle lateral to the intertubercle groove
d. Distal tibia
i. Two finger widths above medial malleolar prominence
3. Prepare EZ-IO driver and needle
4. Insert EZ-IO
a. Stabilize insertion site
b. Position driver 90 to bone surface
c. Push needle through the skin until it contacts bone
d. Evaluate needle for 5mm mark
e. Power the driver and insert needle until hub is flush or lack of resistance is felt
f. Remove driver and stylet from the catheter
5. Confirm position and patency
a. Flush with 10 ml NS (child<40 kg: use 5 ml NS)
b. Ensure catheter standing at 90 and firmly seated
c. No evidence of extravasation
d. Connect tubing utilizing the EZ-IO right angle extension piece and begin infusion
e. Pressure infusion may be needed
6. Secure hub utilizing EZ-IO transparent securement device
7. [Paramedic] If patient is conscious, administer LIDOCAINE 50mg IO for local analgesia
Note:
CONTRAINDICATIONS
1.
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b.
c.
d.
GENERAL MEDICAL
General Scope: Protocol for treatment of patients with medical emergencies
Applies to: All Medical Staff
Protocol:
1.
2.
3.
4.
5.
01-18-2016
GENERAL TRAUMA
General Scope: Protocol for treatment of all patients with potential traumatic injuries.
Applies to: All Medical Staff
Protocol:
1. Perform routine trauma assessment
2. Consider Trauma Activation (Appendix D-1) with transport to nearest appropriate trauma
center as per state trauma guidelines
3. Spinal immobilization
4. Airway support as needed, see Airway Management Protocol
5. Respiratory Failure Protocol as needed
6. See Needle Decompression Protocol as needed
7. Splint flail segments and apply occlusive dressing for sucking chest wound
a. Consider intubation
8. Direct pressure for external hemorrhage
a. Consider tourniquet for uncontrolled hemorrhage
b. Consider hemostatic agent per Hemostatic Agent Protocol
9. [EMT-I/AEMT/Paramedic] Establish IV/IO per Vascular Access Protocol
a. Avoid excessive fluid administration
b. Goal of maintaining SBP~100mmHg
c. See Blood Pressure Management Protocol
10. See Shock Protocol
11. Splint extremity fractures
12. Use a pelvic binder or wrap and secure a sheet around the pelvis for suspected pelvic
fractures and splint lower extremity fractures
13. See Pain Management Protocol
01-18-2016
HEAD INJURY
General Scope: Protocol for treatment of all patients with potential head injuries.
Applies to: All Medical Staff
Protocol:
1.
2.
3.
4.
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Protocol:
1. Identify source of bleeding
a. Place proximal tourniquet if appropriate
b. Wipe pooled blood from wound if necessary
2. Apply hemostatic gauze, packing into wound as per manufacturers instructions
3. Pack entire length of gauze into wound
4. Apply direct pressure for 1-3 minutes with hemostatic gauze
a. If bleed-through occurs entire dressing must be removed before repacking
5. Apply standard dressing and bandage
Note: Specific brand of hemostatic gauze must not cause thermal reaction.
01-18-2016
HYPERKALEMIA
General Scope: Protocol for treatment of patients who are or suspected to be hyperkalemic
Applies to: All Medical Staff
Protocol:
1. Perform routine medical assessment
2. Identify as symptomatic: Patients with profound weakness or shock with peaked T-waves,
history of dialysis, renal failure, severe burns/trauma/crush injury, or laboratory confirmed
diagnosis of hyperkalemia
3. Airway support as needed, see Airway Management Protocol
4. Obtain 12 lead EKG
5. [EMT-I/AEMT/Paramedic] Establish IV/IO per Vascular Access Protocol
6. [Paramedic/Med Control] Calcium Gluconate 1gram/10cc in 100ml D5W or NS over 10
minutes
a. This is the preferred treatment for pre-arrest or arrest situations
b. Do not mix this with sodium bicarbonate
7. [Paramedic/Med Control] ALBUTEROL 20mg via nebulizer
8. [Paramedic/Med Control] SODIUM BICARBONATE 50mEq IV over 10 minutes
a. May repeat up to 2 total doses
b. Avoid in dialysis and CHF patients
c. Do not mix with calcium gluconate.
9. [Paramedic/Med Control] LASIX 40-80mg IV
a. Avoid in dialysis patients
Note:
1. Cardiac effects (may or may not be present)
a. 5.6-6.0mEq/L - peaked T waves due to increased repolarization
b. 6.0-6.5mEq/L - prolonged PR & QT intervals
c. 6.5-7.0mEq/L - diminished P waves and depressed ST segments; may result in
an intracardiac block affecting in the following order: atria, AV node, ventricles
d. 7.5-8.0mEq/L - P waves disappear, QRS complex widens, S & T waves tend to
merge
e. 10-12mEq/L - classic sine wave occurs which represents loss of P wave and
wide QRS complexes.
2. Other effects
3. Skeletal muscle weakness to flaccid paralysis with preservation of diaphragm muscle
function
a. Paresthesias
b. Respiratory depression
01-18-2016
HYPOTHERMIA
General Scope: Protocol for treatment of all patients with potential hypothermia.
Applies to: All Medical Staff
Protocol:
1. Perform routine medical and trauma assessment
2. If patient is responsive
a. Remove wet clothing, cover with warm blankets, apply heat packs to axilla, groin,
neck, and thorax
b. If signs of frostbite:
i. Protect injured part (blisters) with light sterile dressings. Avoid pressure to
area
ii. Cover affected part with warm blankets and prevent re-exposure to cold or
refreezing of part
c. [EMT-I/AEMT/Paramedic] Establish IV/IO per Vascular Access Protocol
d. [EMT-I/AEMT/Paramedic] Give up to 2 liters of warmed NS IV
3. If patient is unresponsive
a. Airway support as needed, see Airway Management Protocol
b. Respiratory Failure Protocol as needed
c. [EMT-I/AEMT/Paramedic] Establish IV/IO per Vascular Access Protocol
d. [EMT-I/AEMT/Paramedic] Give up to 2 liters of warmed NS IV
e. If bradycardic do not start CPR
f. If patient is pulseless
i. Check for pulse, respirations, and/or viable rhythm for at least 1 minute
ii. If patient is pulseless:
1. start CPR
2. Follow appropriate cardiac arrest protocol
3. Consider transport as soon as possible for rewarming
***The field resuscitation may be withheld if the victim has obvious lethal injuries or if the body
is frozen so that nose and mouth are blocked by ice and chest compression is impossible.
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IFT OF INSULIN
General Scope: Protocol for the IFT transport of Insulin drip initiated by sending hospital
Applies to: Paramedic/ Critical Care Paramedic
Protocol:
1. Obtain written order for rate and total volume of Insulin to be infused, confirm with
RN or physician.
2. Check blood sugar levels Q15 or per sending facilities written order
Indications:
1. Elevated blood glucose
2. Diabetic ketoacidosis
3. Hyperkalemia
Precautions:
1. Administration of excessive dose may induce hypoglycemia. Glucose should be available
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1.
2.
3.
4.
5.
01-18-2016
INTRANASAL MEDICATIONS
General Scope: Procedure for administration of intranasal medications via the Mucosal Atomization
Device (MAD). Acceptable intranasal medications are: [Paramedic] Fentanyl, Versed, Narcan, and
Glucagon.
Applies to: EMT-I** / Paramedic (** Optional use by service and requires Prior Written Approval of
the Operational Plan by the State EMS Office and Medical Director Approval and Documentation of
Training.)
Protocol:
1. Determine MAD/Intranasal indications
2. Rule out contraindications
a. Epistaxis
b. Nasal trauma
c. Nasal septal abnormalities
d. Significant nasal congestion/discharge
3. Draw up medication not to exceed 2ml total volume
4. Attach MAD to syringe and place MAD in nostril
5. Briskly compress syringe to administer atomized medication
a. Point outwards and upwards
b. Do not to exceed 1ml total volume per nostril
Medications may be repeated in 5-10 minutes as needed and
indicated
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18.
Size
3
4
5
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Description
4-5 feet height
5-6 feet height
6+ feet height
Color
Yellow
Red
Purple
Inflation
45-60 ml
50-70 ml
60-80 ml
If orders are given that the paramedics feel to be unreasonable, medically inaccurate, and/or not within
their capabilities, the paramedics DO NOT have to do that which they know by their training, skill, and
experience would be detrimental to the patient.
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01-18-2016
Diltiazem in contraindicated: A. Sick-Sinus syndrome B. 2nd or 3rd degree heart block C. WPW or short PR
syndrome
Common side effects of diltiazem: A. Symptomatic hypotension. B. Flushing. C. Burning or itching at injection
site.
Lopressor should be used with caution if evidence of CHF/Pulmonary edema
Amiodarone precautions:
A. Hypotesion secondary to vasodilation
B. May prolong QT interval
C. Negative inotropic effects
D. Use with caution in renal failure; long T 1/2lige
01-18-2016
NASOGASTRIC/OROGASTRIC TUBE
General Scope: Procedure for NG Tube placement.
Applies to: Paramedics
Protocol:
1. Assessment reveals the following:
a. Vomiting and/or abdominal pain with distended, tympanic abdomen and possible
frequent high-pitched bowel sounds
b. Distended abdomen after resuscitative efforts (air-filled stomach)
c. Avoid in patients with significant facial and head injuries
2. If conscious see Sedation Protocol and Pain Management Protocol
3. Determine NGT size
a. Adult: 12-18Fr
b. Child: 8-10Fr
4. Maintain patient with head in neutral or slightly flexed position
5. Determine length of insertion (tip of nose -> earlobe -> bottom of sternum)
6. Lubricate NGT with water-based lubricant
7. Insert NGT through nose to determined length
a. May use mouth as alternative route in intubated patients
8. Visualize mouth for coiled NGT
9. Inject air through NGT and auscultate over epigastrium
10. Tape NGT to nose and connect to low continuous suction
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01-18-2016
NEEDLE CRICOTHYROIDOTOMY
General Scope: Procedure for needle cricothyroidotomy. This is a last option for airway management
and requires approval from medical control. Needle cricothyroidotomy is the only allowable surgical
airway for children less than ten years of age.
Applies to: Paramedics
Protocol:
1. Determine need and contact medical control
2. Palpate cricothyroid membrane and clean area with antiseptic wipe
3. Puncture membrane with large bore catheter, advance caudally drawing back on syringe
until air return
4. Withdraw needle and attach 3.0mm pediatric ETT adapter with BVM
5. Auscultate chest and secure device
01-18-2016
NEEDLE THORACENTESIS
General Scope: Procedure for needle chest decompression
Applies to: Paramedics
Protocol:
1. Determine need
2. If conscious see Sedation Protocol
3. Cleanse site with antiseptic wipe
a. 5th intercostal space mid-axillary is preferred
b. 2nd intercostal space mid-clavicular is secondary
4. Insert 12g or 14g catheter
5. Listen for rush of air
6. Remove needle leaving catheter in place
7. Auscultate chest and secure device
01-18-2016
NEONATAL RESUSCITATION
General Scope: Protocol for resuscitation of a neonatal patient.
Applies to: All Medical Staff
Protocol:
1.
2.
3.
4.
5.
6.
7.
8.
9.
01-18-2016
PAIN MANAGEMENT
General Scope: Protocol for treatment of patients who are or suspected to be experiencing pain
Applies to: All Medical Staff
Protocol:
1.
2.
3.
4.
5.
01-18-2016
POSTPARTUM HEMORRHAGE
General Scope: Protocol for post-delivery hemorrhage.
Applies to: All Medical Staff
Protocol:
1.
2.
3.
4.
5.
6.
7.
8.
01-18-2016
PRE-ECLAMPSIA / ECLAMPSIA
General Scope: Protocol for pre-eclamptic or eclamptic patients.
Applies to: All Medical Staff
Protocol:
1.
2.
3.
4.
01-18-2016
PEDIATRIC ASYSTOLE/PEA
General Scope: Protocol for treatment of a pediatric patient in asystolic cardiac arrest
Applies to: All Medical Staff
Protocol:
1. Perform routine medical assessment
2. Initiate CPR and continue throughout resuscitation with minimal interruptions
3. Consider possible causes and treatments
a. Hypoxia ventilation see Airway Management Protocol
b. Preexisting acidosis Ventilations, consider [Paramedic] SODIUM BICARBONATE 1
Amp IV
c. Drug overdose see Poisoning and Overdose Protocol
d. Hypothermia see Hypothermia Protocol
e. Hyperkalemia see Hyperkalemia Protocol
4. [Paramedic] Confirm asystole in two leads
a. If rhythm is unclear, see Pediatric V-Fib/Pulseless V-Tach Protocol
5. [EMT-I/AEMT/Paramedic] Establish IV/IO per Vascular Access Protocol
6. Establish airway per Respiratory Failure Protocol
7. [Paramedic] Administer EPINEPHRINE (1:10,000) 0.01mg/kg IV/IO Q 3-5 minutes
8. Update Medical Control
a. May request termination of efforts
01-18-2016
PEDIATRIC B RADYCARDIA
General Scope: Protocol for treatment of a pediatric patient with symptomatic bradycardia
Applies to: All Medical Staff
Protocol:
1. Perform routine medical assessment
2. Monitor SpO2
a. Airway support as needed per Airway Management Protocol
3. If HR<60 start CPR
4. Identify patient as having serious signs or symptoms
a. Obtain/review EKG if available
5. [EMT-I/AEMT/Paramedic] Establish IV/IO per Vascular Access Protocol
6. [Paramedic] Administer EPINEPHRINE 0.01mg/kg (1:10,000) IV/IO Q 3-5 minutes
7. [Paramedic] Administer ATROPINE 0.02mg/kg IV/IO Q 3-5 minutes
a. May repeat once
b. Min: 0.1mg single dose
c. Max: 0.5 mg single dose
[Paramedic] Consider Trancutaneous Pacing (rate at 100-120)
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ROSC BENCHMARKS
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PULMONARY EDEMA
General Scope: Protocol for management of patients with suspected pulmonary edema
Applies to: All Medical Staff
Protocol:
1.
2.
3.
4.
5.
6.
7.
8.
Note:
Cardiogenic Pulmonary Edema (CPE)
2. Conditions associated with CPE
a. LV failure from acute MI, cardiomyopathies and valvular heart disease
b. Volume overload
2. Clinical features of CPE include:
a. Cough
b. Diaphoresis
c. Dyspnea
d. Fatigue
e. Wheezing
f. Pink tinged frothy sputum
Avoid use of NTG if any history of PDE 5 inhibitor (Viagra, Levitra, Cialis) use in the past 48 hours
01-18-2016
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9.
Identify service, unit number, radio frequency, and personnel (if applicable)
Identify level of care being provided
Communicate patients age, sex, and level of consciousness
Communicate severity of condition
a. Include applicable activation of specialized services (trauma, cardiac, stroke)
Communicate patients chief complaint and/or primary impression
Communicate history of injury/illness and pertinent past medical history
Relate pertinent assessment and finding
Communicate any treatment initiated
a. EMS staff can request orders from on-line medical control at this time, but it is often
more expedient to initiate a request for orders prior to giving patient report
Give estimated time of arrival
01-18-2016
2.
3.
01-18-2016
RSI CHECKLIST
Assesses airway for difficulty. (LEMON / Malampati)
Perform neurologic exam before paralytics are administered.
Pre-oxygenates w/ NRB or BVM.
Prepares intubation equipment. (Laryngoscope, ET Tube, syringe, securing device, intubating stylette)
Readies alternative airways. (King airway, surgical airway)
Monitor vital signs. (SaO2, EKG, ETCO2)
Prepare suction. (Yankauer within reach [under shoulder], turn on, check canister and lid)
Prepare bag-valve mask. (Attached to oxygen, mask is ALWAYS present, PEEP valve attached)
Ensure IV access. (Patent, appropriate size/location, fluid administration)
Ensures proper positioning. (Sniffing position: ear to sternal notch/face parallel to ceiling)
Performs rapid sequence induction.
Places basic airway adjunct. (Nasopharyngeal airway or oropharyngeal airway)
Performs apneic oxygenation.
Lubricate endotracheal tube, stylette, and blade.
Performs endotracheal intubation without significant change in clinical status.
Retains necessary equipment in case of problem. (Syringe, BVM mask, laryngoscope)
Confirms placement with epigastric sounds, lung sounds, and waveform capnography.
Secures device using commercial device or properly placed tape.
Provides sedation and pain management as needed. Re-paralyze if necessary.
Re-assesses through completion of patient contact. (Vital signs and interventions)
01-18-2016
RSI BENCHMARK
Scene time less than 30 minutes for RSI
Documentation of patients weight
Appropriate EMD (P1 response)
3 or less intubation attempts
ET outcome %
ET success rate %
Advanced airway outcome
ETCO2 confirmation
EKG strips attached to chart
Vitals q 10 minutes
Preoxygenation protocol prior to RSI
Sedation when not contraindicated
01-18-2016
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RESPIRATORY FAILURE
General Scope: Protocol for treatment of a patient in respiratory failure
Applies to: All Medical Staff
Protocol:
1. Perform routine medical assessment
2. See Airway Management Protocol as needed
3. Observe for signs/symptoms of respiratory failure
a. Failure to oxygenate and/or ventilate, severe respiratory fatigue, inability to
successfully use CPAP, or otherwise noted to be in clinical respiratory failure
4. [Paramedic] Assess expected success of intubation
5. Have rescue airway available
6. [Paramedic]If endotracheal intubation success likely
a. See Rapid Sequence Intubation Protocol
i. If less likely success, consider RSI without Zemuron
7. If failed intubation (3 unsuccessful attempts by skilled providers)
a. Consider BVM
b. Consider King Airway
c. [Paramedic/Med Control] Consider Surgical Cricothyroidotomy Protocol
Note:
Signs of impending respiratory failure include:
01-18-2016
RESTRAINT USE
General Scope: Procedure for restraint of a combative patient
Applies to: All Medical Staff
Protocol:
1.
2.
3.
4.
5.
6.
01-18-2016
SCENE REHABILITATION
General Scope: Protocol for rehabilitation of rescue personnel when requested to a standby
Applies to: All Medical Staff
Protocol:
1.
2.
3.
4.
01-18-2016
SEDATION
General Scope: Protocol for treatment of patients who require sedation in the prehospital setting. All
patients who receive sedation should have continuous monitoring of vital signs including cardiac
monitoring.
Applies to: All Medical Staff
Protocol:
1.
2.
3.
4.
01-18-2016
SEIZURE
General Scope: Protocol for treatment of patients who are or suspected to be experiencing seizures
Applies to: All Medical Staff
Protocol:
1.
2.
3.
4.
01-18-2016
SHOCK
General Scope: Protocol for management of shock in all patients
Applies to: All Medical Staff
Protocol:
1. Control obvious hemorrhage
2. Position patient supine when possible
3. [EMT-I/AEMT/Paramedic] Establish IV/IO per Vascular Access Protocol
a. 2 access points if evidence of Class II or greater shock
b. Initial fluid challenge with NS with a SBP goal of > 80 in trauma patients (permissive
hypotension except in patients with significant head injuries), 90 in medical patients
4. [Paramedic/Medical Control] For hemorrhagic shock: Tranexamic acid (TXA) 1g in 100ml D5W IV
over 10 minutes (faster may result in hypotension); use a filter needle to draw up
a. Follow by an infusion of 1g in 500ml NS over 8 hours (at receiving facility)
b. Indications: Evidence of acute blood lossClass II or greater
c. Administration as soon as possible but no later than 3 hours after initial injury
d. Exclusions:
i. Patients < 16
ii. Known time of injury greater than 3 hours or unknown time
iii. DIC
iv. Recent history of thrombosis or thromboembolism (DVT, PE, embolic stroke).
5. If evidence of anaphylaxis, see Anaphylaxis/Allergic Reaction Protocol
6. Shock Classifications
CLASS I
CLASS II
CLASS III
CLASS IV
Up to 750
750-1500
1500-2000
>2000
Up to 15%
15-30%
30-40%
>40%
<100
>100
>120
>140
Normal
Normal
Decreased
Decreased
Normal or
Decreased
Decreased
Decreased
14-20
20-30
30-40
>35
>30
20-30
5-15
Negligible
Slightly
Mildly
Anxious and
Confused and
anxious
anxious
confused
lethargic
Pulse Rate
Blood Pressure
Pulse Pressure (mmHg)
increased
Respiratory Rate
Urine Output (mL/hr)
CNS/Mental Status
01-18-2016
Crystalloid
Crystalloid
Crystalloid
Crystalloid
and blood
and blood
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Spinal Examination
General Scope: This procedure details the spinal examination process and must be used in conjunction
with the spinal precautions clearance protocol.
Applies to: Paramedic/Transport Ambulance
Protocol:
a. Explain to the patient the actions you are going to take. Ask the patient to
immediately report any pain, and to answer questions with a yes or no
rather than shaking the head
b. With the patients spine supported to limit movement, begin palpation at the
base of the scull at the midline of the spine
c. Palpate the vertebrae individually from the base of the skull to the bottom of the
sacrum
d. On palpation of each vertebral body, look for evidence of pain and ask the
patient if they are experiencing pain. If evidence of pain along the spinal column
is encountered, the patient should be immobilized
e. If the capable patient is found to be pain free, ask the patient to turn their head
first to one side (so that the chin is pointing toward the shoulder on the same
side as the head is rotating) then, if pain free, to the other. If there is evidence of
pain the patient should be immobilized
f.
01-18-2016
With the head rotated back to its normal position, ask the patient to flex and
extend their neck. If there is evidence of pain the patient use spinal precautions
protocol
Note:
01-18-2016
SPIT HOOD
General Scope: Protocol for use of protective hoods. This protocol should be used for patients whom
are combative and/or aggressive, and purposely attempting to spit on providers or other public safety
personnel. Spitting carries potential risk of disease transmission. Use of a protective hood minimizes
said risk.
Applies to: All Medical Staff
Protocol:
1. Use of one-piece surgical mask or oxygen mask is preferred for minimizing risk of disease
transmission by patients whom are purposely spitting.
2. CONDITIONS FOR USE
a. DO NOT USE unless patient is under control and restrained.
b. DO NOT USE on anyone that is vomiting, having difficulty breathing, or is bleeding
profusely from the area around the mouth or nose.
c. Patient must be under constant visual supervision and should never be left
unattended.
d. Remove patients jewelry and eyewear before application.
e. If there is difficulty applying due to large size head, discontinue use.
f. Conditions for use should be constantly monitored during patient encounter.
3. PROCEDURE FOR USE
a. Open and remove the Tranzport Hood
b. Place the Tranzport hood over the head of the person with the mesh fabric
positioned just below the eyes to allow the person to see.
c. For the best fit, place the center elastic under the nose and over the ears. For better
protection, the elastic may be placed above the nostrils.
d. Carefully push the plastic Secure-Lock Tab down toward the top of the head while
holding the top of the mesh fabric. This should take the slack out of the top and help
secure the Tranzport Hood in position.
i. ** DO NOT push so tightly as to be uncomfortable or impair the vision of the
wearer.
e. See manufacturer instructions included in packaging for visual representation of
procedure for use.
f. Patient should be transported in either left or right lateral position.
g. CONTINUOUSLY monitor patients airway, respiratory status, and pulse oximetry.
h. IMMEDIATELY remove surgical mask, oxygen mask, or Tranzport Hood if any
question of airway patency or potential compromise.
01-18-2016
SURGICAL CRICOTHYROIDOTOMY
General Scope: Procedure for surgical cricothyroidotomy. This is a last option for airway management
and requires approval from medical control. Surgical cricothyroidotomy is contraindicated in patients
< 10 years old.
Applies to: Paramedics
Protocol:
1.
2.
3.
4.
5.
6.
7.
01-18-2016
Note:
Amiodarone Precautions
Hypotension secondary to vasodilatation
May prolong QT interval
Negative inotropic effects
Use with caution in renal failure; long T1/2 life
01-18-2016
TERMINATION OF RESUSCITATION
General Scope: Procedure for terminating resuscitation efforts in cardiac arrest
Applies to: All Medical Staff
Protocol:
1. Except in conditions in Determination of Death Protocol, CPR is to be initiated and
maintained until one of the following occurs
a. Resuscitation efforts have been transferred to other persons of at least equal skill
and training
b. Effective ROSC and ventilation have been restored
c. The rescuers are physically unable to continue efforts
d. Medical Control orders efforts to stop
i. If transport has been initiated, efforts must continue until patient care has
been turned over to the receiving hospital
2. Update Medical Control
01-18-2016
01-18-2016
TRAUMA IN P REGNANCY
General Scope: Protocol for treatment of all potentially pregnant patients with potential trauma.
Applies to: All Medical Staff
Protocol:
1. Perform routine medical and trauma assessment
2. See General Trauma Protocol
3. Position patient on left side unless a spinal injury is suspected (minimize uterine
compression on the inferior vena cava)
4. If patient is immobilized on a long back board:
a. Tilt backboard to left side
b. Elevate right buttock and push uterus to the left
5. [EMT-I/AEMT/Paramedic] Establish IV/IO per Vascular Access Protocol
6. Maintain blood pressure, see Blood Pressure Management Protocol
a. SBP & DBP is 5-15mmHg less starting in second trimester
b. HR is 15-20 BPM more during third trimester
c. Shock is not always obvious in the pregnant patient (Because of an increase in
circulating blood volume during pregnancy, the pregnant female will show signs of
hypovolemia later in their course)
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VASCULAR ACCESS
General Scope: Procedure for vascular access.
Applies to: Intermediate Technicians, AEMT**, Paramedics
** Optional use by service and requires Prior Written Approval of the Operational Plan
by the State EMS Office and Medical Director Approval and Documentation of Training.
Protocol:
1. [EMT-I/AEMT/Paramedic] Establish peripheral IV
a. 2 IVs if indicated and possible
b. 16g or larger if indicated and possible
i. Trauma activations
ii. Cardiac arrest
iii. GI bleed
iv. Hypovolemia
2. [EMT-I/AEMT**/Paramedic] If unsuccessful, consider EZ-IO or [Paramedic]external jugular
IV
a. [Paramedic] Consider external jugular IV (patient age>6)
i. Place patient supine or head down
ii. Locate vein
iii. Cleanse area with antiseptic wipe
iv. Make venipuncture midway between angle of jaw and mid-clavicular line
v. Confirm placement
vi. Attach IV tubing and secure to patients neck
b. Consider EZ-IO, see EZ-IO Protocol
3. [Paramedic] If EZ-IO failure, attempt manual IO
a. Support leg with knee slightly raised
b. Cleanse area with antiseptic wipe
c. Inset needle through skin at 90 angle on tibial plateau
d. Insert needle into bone marrow cavity with twisting motion
e. Upon loss of resistance remove stylet, aspirate, then attach IV
f. Secure needle
01-18-2016
01-18-2016
*Pump Set
*Drug Rate
2 ml/hr
5 mcg/min
3 ml/hr
10 mcg/min
4 ml/hr
15 mcg/min
6 ml/hr
20 mcg/min
8 ml/hr
25 mcg/min
9 ml/hr
30 mcg/min
11 ml/hr
35 mcg/min
12 ml/hr
40 mcg/min
14 ml/hr
45 mcg/min
15 ml/hr
50 mcg/min
18 ml/hr
60 mcg/min
21 ml/hr
70 mcg/min
24 ml/hr
80 mcg/min
30 ml/hr
100 mcg/min
36 ml/hr
120 mcg/min
42 ml/hr
140 mcg/min
48 ml/hr
160 mcg/min
54 ml/hr
180 mcg/min
60 ml/hr
200 mcg/min
01-18-2016
mcg/kg/min
5
7
10
15
20
Pump Setting
Dose
01-18-2016
40
15
21
30
45
60
50
18.75
26.25
37.5
56.25
75
60
22.5
31.5
45
67.5
90
70
26.25
36.75
52.5
78.75
105
80
30
42
60
90
120
90
33.75
47.25
67.5
101.25
135
100
37.5
52.5
75
112.5
150
110
41.25
57.75
82.5
123.75
165
120
45
63
90
135
180
130
48.75
68.25
97.5
146.25
195
140
52.5
73.5
105
157.5
210
150
56.25
78.75
112.5
168.75
225
160
60
84
120
180
240
170
63.75
89.25
127.5
191.25
255
Rate
15 ml/hr
1 mg/min
30 ml/hr
2 mg/min
45 ml/hr
3 mg/mi
60 ml/hr
4 mg/mn
Pump Set
Rate
40 ml/hr
1 mg/min
01-18-2016
9.
10.
11.
12.
01-18-2016
a. Metal cannula, fenestrated (cuffless) or button device: replace with 6-7F ETT,
whichever can be placed with the least effort/trauma
b. Non-fenestrated cuffed trach: insert inner cannula and inflate balloon; if no inner
cannula available, go to 2A.
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01-18-2016
01-18-2016
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01-18-2016
01-18-2016
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01-18-2016
11.
12.
13.
14.
15.
16.
17.
18.
19.
20.
21.
Gather equipment.
Explain procedure to the patient
Assist patient into supine position with legs spread and feet together
Open catheterization kit and catheter
Prepare sterile field, apply sterile gloves
Check balloon for patency.
Generously coat the distal portion (2-5 cm) of the catheter with lubricant
Apply sterile drape
If female, separate labia using non-dominant hand. If male, hold the penis with the nondominant hand. Maintain hand position until preparing to inflate balloon.
Using dominant hand to handle forceps, cleanse peri-urethral mucosa with cleansing solution.
Cleanse anterior to posterior, inner to outer, one swipe per swab, discard swab away from
sterile field.
Pick up catheter with gloved (and still sterile) dominant hand. Hold end of catheter loosely
coiled in palm of dominant hand.
In the male, lift the penis to a position perpendicular to patient's body and apply light upward
traction (with non-dominant hand)
Identify the urinary meatus and gently insert until 1 to 2 inches beyond where urine is noted
Inflate balloon, using correct amount of sterile liquid (usually 10 cc but check actual balloon size)
Gently pull catheter until inflation balloon is snug against bladder neck
Connect catheter to drainage system
Secure catheter to abdomen or thigh, without tension on tubing
Place drainage bag below level of bladder
Evaluate catheter function and amount, color, odor, and quality of urine
Remove gloves, dispose of equipment appropriately, wash hands
Document size of catheter inserted, amount of water in balloon, patient's response to
procedure, and assessment of urine
01-18-2016
01-18-2016
01-18-2016
Find out the patients last known well time from most reliable source
Get and report a blood sugar reading
Get and report blood pressure status
Are they taking an oral anticoagulant/blood thinner [Coumadin,
Dabigatran (Pradaxa), Rivaroxaban, (Xarelto)]?
(Stroke) Alert the hospital that you are bringing a potential stroke in
progress
Identify & report any Yes answers regarding IV tPA
01-18-2016
01-18-2016
Notes:
01-18-2016
01-18-2016
Heparin
Hydromorphone (dilaudid)
Insulin
Ipratropium (atrovent)
Ketamine (ketalar)
Ketorolac (toradol)
Labatelol
Levalbuterol (xopenex)
Lidocaine (xylocaine)
Lorazepam (ativan)
Magnesium sulfate
Mannitol
Methylprednisolone (solu-medrol)
Metoclopramide (reglan)
Metoprolol (lopressor)
Midazolam (versed)
Nalbuphine (nubain)
Naloxone (narcan)
Morphine
Nitroglycerin
Nitrous oxide
Ondansetron (zofran)
Oxygen
Oxytocin (pitocin)
Pancuronium (pavulon)
Pralidoxime (2-pam chloride)
Procainamide
Prochlorperazine (compazine)
Pantoprazole (protonix)
Rocuronium (zemuron)
Sodium bicarbonate
Succinylcholine (anectine)
Terbutaline
Thiamine
tPA(tissue plasminogen activator)
Vasopressin (pitressin)
Vecuronium (norcuron)
Ziprasidone (geod
MEDICATIONS .
0.45% SODIUM CHLORIDE
ACTION: Replaces free water and electrolytes
INDICATIONS:
Patients with diminished renal or cardiovascular function for whom rapid rehydration is not indicated
CONTRAINDICATIONS:
Cases in which rapid rehydration is indicated
PRECAUTION:
1. Clinical evaluation and periodic laboratory determinations are necessary to monitor changes in fluid
balance, electrolyte concentrations and acid-base balance during prolonged parenteral therapy or
whenever the condition of the patient warrants such evaluation.
2. Caution must be exercised in the administration of parenteral fluids, especially those containing sodium
ions to patients receiving corticosteroids or corticotropin.
3. Do not administer unless solution is clear and container is undamaged. Discard unused portion
ADVERSE REACTIONS AND SIDE EFFECTS:
1. Increased urination
2. Pain
3. Redness
4. Swelling at the injection site
5. Swelling of hands or ankles
6. Muscle twitching
ADULT ADMINISTRATION:
Dependent on patients condition and situation being treated.
PEDIATRIC ADMINISTRATION:
The safety and effectiveness in the pediatric population are based on the similarity of the clinical conditions of
the pediatric and adult populations. In neonates or very small infants the volume of fluid may affect fluid and
electrolyte balance.
SPECIAL CONSIDERATIONS:
1. May only be used by Critical Care Paramedics.
2. Solutions containing sodium ions should be used with great care, if at all, in patients with congestive heart
failure, severe renal insufficiency and in clinical states in which there exists edema with sodium retention.
3. Excessive administration of potassium-free solutions may result in significant hypokalemia.
4. In patients with diminished renal function, administration of solutions containing sodium ions may result
in sodium retention.
5. The intravenous administration of these solutions can cause fluid and/or solute overloading resulting in
dilution of serum electrolyte concentrations, overhydration, congested states or pulmonary edema.
6. The risk of dilutional states is inversely proportional to the electrolyte concentrations of administered
parenteral solutions. The risk of solute overload causing congested states with peripheral and pulmonary
edema is directly proportional to the electrolyte concentrations of such solutions.
3-19-15
AZITHROMYCIN (ZITHROMAX)
ACTION:
Bactericidal and bacteriostatic to select organisms including anaerobic and facultative gram positive and gram
negative organisms, Chalmydophila and Mycoplasma
INDICATIONS:
1. Treatment of community acquired pneumonia and pelvic inflammatory disease caused by specific
organisms.
2. Non-gonococcal urethritis and cervicitis due to Chlamydia trachomatis
3. Mycobacterial Infections
CONTRAINDICATIONS:
1. Known Hypersensitivity
2. Erythromycin allergy
3. Any macrolide antibiotic allergy
4. Ketolide antibiotic allergy
PRECAUTIONS:
1. Monitor vitals closely
2. May aggravate CHF
3. Renal insufficiency
ADVERSE REACTIONS AND SIDE EFFECTS:
1. Abdominal pain
2. Arrhythmias
3. Dizziness
4. Hypotension
5. Facial edema
6. Jaundice
7. Nausea
8. Vomiting
9. Diarrhea
ADULT ADMINISTRATION:
1. Physician ordered dose.
2. 500 mg daily for minimum of prescribed days
PEDIATRIC ADMINISTRATION:
Not for Pediatric patients
SPECIAL CONSIDERATIONS:
1. May only be administered by Critical Care Paramedics.
2. Do not use anti-diarrhea products or narcotic pain medications if you have any of the side effects because
these products may make them worse
3. Do not take antacids that contain aluminum or magnesium within 2 hours before or after you take
azithromycin they will make azithromycin less effective
3-19-15
SPECIAL NOTES:
1. May only be administered by Paramedic or Critical Care Paramedics.
2. If infiltration occurs, notify physician at receiving hospital immediately upon arrival so that antidotal
therapy can begin immediately.
3-19-15
CEFTRIAXONE (ROCEPHIN)
ACTION:
Preferentially binds to one or more of the penicillin binding proteins located on cell walls of susceptible
organisms. This inhibits third and final stage of bacterial cell wall synthesis, thus killing the bacterium. Similar
to other third-generation cephalosporins, it is effective against serious gram-negative organisms, and also
penetrates the CSF in concentrations useful in treatment of meningitis.
INDICATIONS:
Infections caused by susceptible organisms in lower respiratory tract, skin structures, urinary tract, bones, and
joints; also intra-abdominal infections, pelvic inflammatory disease, uncomplicated gonorrhea, meningitis, and
surgical prophylaxis.
CONTRAINDICATIONS:
1. Hypersensitivity to ceftriaxone or other cephalosporin antibiotics
2. Viral infection
3. S & S of gallbladder disease
4. Neonates with hyperbilirubinemia
5. Neonates receiving calcium-containing infusions or TPN
6. Premature neonates
PRECAUTIONS:
1. Hypersensitivity to penicillin and beta-lactam antibiotics
2. Coagulopathy
3. Impaired vitamin K synthesis
4. Chronic hepatic disease
5. History of GI disease
6. Colitis
7. Renal disease or impairment
8. Pregnancy
ADVERSE REACTIONS AND SIDE EFFECTS:
1. GI (nausea, vomiting, diarrhea)
2. Leukopenia (Lower WBC count)
3. Pain at injection site
ADULT ADMINISTRATION:
1. Physician ordered dose.
2. Moderate to Severe Infections: 1-2 g every 12-24 hrs, max 4 g/day
3. Meningitis: 2 g every 12 hrs
PEDIATRIC ADMINISTRATION:
1. Physician ordered dose.
2. Moderate to Severe Infections: 50-75 mg/kg/day in 2 divided doses (max 2 g/day)
3. Meningitis: 100 mg/kg/day in 2 divided doses (max 4 g/day)
SPECIAL CONSIDERATIONS:
1. May only be administered by Critical Care Paramedics.
2. Infuse over 30 minutes, use smaller needles, larger veins.
3-19-15
CIPROFLOXACIN (CIPRO)
ACTION:
Antibiotic: Inhibits DNA-gyrase, an enzyme required for DNA replication, transcription, repair, and
recombination of bacterial DNA. Effective against many gram-positive and gram-negative organisms
INDICATIONS:
1. UTI
2. Lower respiratory tract infections
3. Skin and skin structure infections
4. Bone and joint infections
5. GI infections or infectious diarrhea
6. Chronic bacterial prostatitis
7. Nosocomial pneumonia
8. Inhalation anthrax
CONTRAINDICATIONS:
1. Known hypersensitivity to ciprofloxacin or other quinolones
2. Syphilis
3. Viral infection
4. Tendon inflammation or tendon pain
5. Lactation
PRECAUTIONS:
1. Known or suspected CNS disorders (i.e., severe cerebral arteriosclerosis or seizure disorders)
2. Myasthenia gravis
3. Myocardial ischemia, a-fib, QT prolongation, CHF
4. GI disease, colitis
5. CVA
6. Uncorrected hypokalemia
7. Patients receiving theophylline derivatives or caffeine
8. Severe renal impairment and crystalluria during ciprofloxacin therapy
9. Patients on coumadin therapy
10. Pregnancy
11. Children
ADVERSE REACTIONS AND SIDE EFFECTS:
1. GI
a. Nausea and vomiting
b. Diarrhea
c. Cramps
d. Gas
e. Pseudomembranous colitis
2. Musculoskeletal
a. Tendon rupture
b. Cartilage erosion
3. CNS
a. Headache
b. Vertigo
3-19-15
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3-19-15
DEXAMETHASONE (DECADRON)
ACTION:
1. Inhibits many of the substances that cause inflammation and inhibits the synthesis of pro-inflammatory
enzymes
2. Potent Anti-inflammatory and immunosuppressant
INDICATIONS:
1. Severe anaphylaxis
2. Asthma
3. COPD
4. Dermatologic diseases
5. Endocrine disorders
6. Gastrointestinal diseases
7. Hematologic disorders
8. Respiratory diseases
9. Rheumatic disorders
CONTRAINDICATIONS:
None in the acute management of anaphylaxis
PRECAUTIONS:
1. Kidney disease
2. Liver disease
3. Low blood minerals
ADVERSE REACTIONS:
1. Hypertension
2. Vertigo
4. Congestive heart failure
5. Hyperglycemia
6. Headache
7. Nausea
8. Hiccups
9. Glaucoma
ADULT ADMINISTRATION:
1. 4-10mg IV/IO, can be administered IM when IV/IO not available
2. Contact medical control for further orders.
PEDIATRIC ADMINISTRATION:
1. 0.2-0.5 mg/kg IV/IO
2. Contact medical control for further orders.
SPECIAL CONSIDERATIONS:
1. May only be administered by Critical Care Paramedics.
2. Only a single dose should be given in the pre-hospital setting.
3. Should be protected from heat.
3-19-15
DOBUTAMINE (DOBUTREX)
ACTION:
1. A sympathomimetic drug used in the treatment of heart failure and cardiogenic shock
2. Increases the force of systolic contraction with little chronotropic activity
INDICATIONS:
1. Inotropic support for short-term treatment of cardiac decompensation due to depressed myocardial
contractility (cardiogenic shock)
2. Used to support BP, CO and renal perfusion in shock.
3. Inotropic support for short-term treatment of CHF when and increased cardiac output, without and
increased cardiac rate, is desired
CONTRAINDICATIONS:
1. Hypersensitivity
2. V-tach
3. Idiopathic hypertrophic subaortic stenosis
4. Hypovolemia
5. Children < 2 yrs
PRECAUTIONS:
1. Preexisting hypertension
2. A-fib
3. Acute MI, unstable angina
4. Severe coronary artery disease
5. Pregnancy
ADVERSE REACTIONS AND SIDE EFFECTS:
1. CNS : Headache, tremors, paresthesias, mild leg cramps, nervousness
2. Cardiovascular: Increased heart rate and BP, premature ventricular beats, palpitation, anginal pain,
arrhythmias
3. GI: Nausea and vomiting
ADULT ADMINISTRATION:
1. Renal
a. 1-5 mcg/kg/min.
2. Severely ill patients
a. Initially 5 mcg/kg/min, increase by 5-10 mcg/kg/min (q10 to 30 min) up to max of 50mcg/kg/min.
3. Cardiac life support
a. Initially 2-5 mcg/kg/min - titrated to effect. Infusion may be increased by 1-4 mcg/kg/minute at 10
to 30 minute intervals until optimal response is obtained.
4. Refractory CHF: administer 0.5 2 mcg/kg/min.
PEDIATRIC ADMINISTRATION:
NOT RECOMMENDED FOR PEDS.
SPECIAL CONSIDERATIONS:
1. May only be administered by Critical Care Paramedics.
2. Administer into large vein to prevent the possibility of extravasation (central line administration).
3-19-15
DROPERIDOL (INAPSINE)
ACTION:
Alters the action of dopamine in the central nervous system causing sedation and the suppression of nausea
and vomiting
INDICATIONS:
1. Nausea and/or vomiting with vertigo.
2. Sedation
CONTRAINDICATIONS:
1. Known hypersensitivity
2. Narrow-angle glaucoma
3. Known or suspected QT prolongation
PRECAUTIONS:
1. Use with caution on patients with:
a. CNS depression
b. Impaired renal function
c. Diabetes
d. Seizures
e. Severe liver disease
2. Use with extreme caution in patients with risk factor for prolonged QT syndrome
a. CHF
b. Bradycardia
c. Diuretic use
d. Hypokalemia
e. Hypomagnesema
ADVERSE REACTIONS AND SIDE EFFECTS:
1. Seizures
2. Extrapyramidal reaction
3. Excessive sedation
4. Arrhythmias
5. Hypotension
6. Tachycardia
ADULT ADMINISTRATION:
1. 0.625-1.25 mg IV over 5 minutes
2. Physician ordered dose
PEDIATRIC ADMINISTRATION:
Physician ordered dose.
SPECIAL CONSIDERATIONS:
1. May only be administered by Paramedics under the Nausea, Vomiting, Vertigo protocol
2. May be administered by Critical Care Paramedics
3-19-15
ENALAPRILAT (VASOTEC)
ACTION:
Enalaprilat, is an angiotensin converting enzyme (ACE) inhibitor. ACE is a peptidyl dipeptidase that
catalyzes the conversion of angiotensin I to the vasoconstrictor substance, angiotensin II. Angiotensin II also
stimulates aldosterone secretion by the adrenal cortex. Inhibition of ACE results in decreased plasma
angiotensin II, which leads to decreased vasopressor activity and also decreased aldosterone secretion.
While the mechanism through which enalaprilat lowers blood pressure is believed to be primarily
suppression of the renin-angiotensin-aldosterone system, enalaprilat has antihypertensive activity even in
patients with low-renin hypertension.
INDICATIONS:
1. Pulmonary edema
2. Congestive heart failure
CONTRAINDICATIONS:
1. Hypersensitivity
2. ACE inhibitor cross sensitivity
3. Angioedema
PRECAUTIONS:
1. Renal impairment
2. Hypovolemia
3. Hyponatremia
4. Aortic stenosis
5. Cerebrovascular or Coronary insufficiency
ADVERSE REACTIONS AND SIDE EFFECTS:
1. CNS: dizziness, fatigue, headache, weakness
2. Respiratory: cough
3. Cardiovascular: hypotension, angina, tachycardia
4. GI: taste disturbances, anorexia, diarrhea
ADULT ADMINISTRATION:
1.25 mg IV or physician ordered dose
PEDIATRIC ADMINISTRATION:
NOT RECOMMENDED FOR PEDS.
SPECIAL CONSIDERATIONS:
Paramedics may only administer Enalaprilat under the Pulmonary Edema protocol and with medical control
orders.
3-19-15
EPTIFIBATIDE (INTEGRILIN)
ACTION:
1. Inhibits platelet aggregation by blocking the glycoprotein IIb/IIIa receptor on activated platelets.
2. Treating unstable angina (chest pain) or certain types of heart attacks.
INDICATIONS:
1. Treatment of acute coronary syndromes (unstable angina, non-Q-wave MI)
2. Patients undergoing percutaneous coronary interventions (PCIs)
CONTRAINDICATIONS:
1. Hypersensitivity
2. Active internal bleeding
3. GI or GU bleeding within 6 weeks
4. Recent major surgery
5. Thrombocytopenia
6. Intracranial neoplasm
7. Intracranial bleeding within 6 months
8. Renal dialysis
9. Severe hypertension (systolic BP> 200 or diastolic BP > 110)
10. Aneurysm
11. Hemorrhagic stroke or other stroke within 30 days
PRECAUTIONS:
1. Hypersensitivity to related compounds (abciximab, tirofiban, lamifiban)
2. Patients that have an increased risk of bleeding
3. Pregnancy and lactation
4. Maintaining Target aPTT and ACT
5. Arterial and venous punctures, IM injections, urinary catheters, NG tubes, and nasotracheal intubation
should be minimized
ADVERSE REACTIONS AND SIDE EFFETCS:
1. Increased risk of bleeding
2. Hypotension
3. Allergic reaction
ADULT ADMINISTRATION:
1. 180 mcg/kg initial bolus, give over 1-2 minutes
2. 2 mcg/kg/min up to 72 hours, begin immediately after bolus dose
3. Contact medical control for further orders.
PEDIATRIC ADMINISTRATION:
Not recommended for PEDS.
SPECIAL CONSIDERATIONS:
1. May only be administered by Critical Care Paramedics.
2. Safety and effectiveness in children are not established
3. Use vented tubing
4. Use caution in patients taking oral anticoagulants or NSAID medications
3-19-15
ESMOLOL (BREVIBLOC)
ACTION:
1. Antiarrhythmic properties occur at the AV node. Decreases heart rate, decreases AV conduction
2. Beta1-selective (cardioselective) adrenergic receptor blocking (Beta Blocker) agent with a very short
duration of action (elimination half-life is approximately 9 minutes)
INDICATIONS:
1. Short term treatment in the control of heart rate for patients with MI.
2. Control ventricular rate in a-fib and a-flutter
3. Stable, narrow complex tachycardias if rhythm remains uncontrolled or unconverted by adenosine or vagal
maneuvers or if SVT is recurrent
CONTRAINDICATIONS:
1. Hypersensitivity to Esmolol
2. Heart block greater than first degree
3. Sinus bradycardia
4. Cardiogenic shock
5. Decompensated CHF
6. Acute bronchospasm (asthma and COPD)
PRECAUTIONS:
1. History of allergy
2. History of CHF
3. History of pulmonary disease such as bronchial asthma; COPD; pulmonary edema
4. History of diabetes mellitus
5. History of kidney function impairment
6. Elderly
7. Pregnancy, lactation
ADVERSE REACTIONS AND SIDE EFFECTS:
1. CNS
a. Headache
b. Dizziness
c. Confusion
d. Agitation
2. CV
a. Hypotension (dose related)
b. Bradyarrhythmias
c. Flushing
d. Myocardial depression
3. GI
a. Nausea and vomiting
4. Respiratory
a. Dyspnea
b. Wheezing
c. Rhonchi
d. Bronchospasm
3-19-15
3-19-15
GENTAMICIN SULFATE
ACTION:
Medicine used to treat severe or serious bacterial infection
INDICATIONS:
1. Sulfite sensitivity
2. Kidney disease
3. Hearing loss or loss of balance due to ear problems
4. Parkinson's disease
5. Neuromuscular disorder such as myasthenia gravis.
CONTRAINDICATIONS:
Hypersensitivity to gentamicin
PRECAUTIONS:
1. Pregnancy
2. The frequency of administration of gentamicin should be reduced in patients with impaired renal function
ADVERSE REACTIONS AND SIDE EFFECTS:
1. Allergic reaction
2. Little or no urine
3. Decreased hearing or ringing in ears
4. Dizziness
5. Numbness
6. Seizures
7. Severe diarrhea
8. Abdominal cramps
9. Neurotoxicity
10. Nephrotoxicity
ADULT ADMINISTRATION:
1. Physician ordered dose.
2. 1.5 to 2 mg/kg loading dose over 1-1.5 hours, followed by 1 to 1.7 mg/kg IV or IM every 8 hours or 5 to 7 mg/kg
IV every 24 hours
PEDIATRIC ADMINISTRATION:
1. Physician ordered dose.
2. 0 to 4 weeks, birth weight <1200 g: 2.5 mg/kg IV or IM every 18 to 24 hours
3. 0 to 1 week, birth weight >=1200 g: 2.5 mg/kg IV or IM every 12 hours
4. 1 to 4 weeks, birth weight 1200 to 2000 g: 2.5 mg/kg IV or IM every 8 to 12 hours
5. 1 to 4 weeks, birth weight >=2000 g: 2.5 mg/kg IV or IM every 8 hours
6. >1 month: 1 to 2.5 mg/kg IV or IM every 8 hours
SPECIAL CONSIDERATIONS:
1. May only be administered by Critical Care Paramedics.
2. Dosage should be adjusted for patients with renal impairment.
3. Monitor IV site for irritation or infiltration
3-19-15
HEPARIN (UNFRACTIONATED)
ACTION:
Anticoagulant
INDICATIONS:
1. Management of Acute Myocardial Infarction (AMI) presenting with STEMI
2. Anticoagulant therapy
3. Thrombosis
CONTRAINDICATIONS:
1. Active bleeding, uncontrollable; except when due to disseminated intravascular coagulation.
2. Severe hypertension (Systolic BP > 200)
3. Bleeding disorders/ known GI bleeding
4. Known Heparin induced thrombocytopenia = (persistent decrease in the number of platelets in the blood
that is often associated with hemorrhagic conditions).
ADVERSE REACTIONS AND SIDE EFFECTS:
1. Allergic reaction/Anaphylaxis.
2. Hemorrhage.
3. Osteoporosis (only with long term, high-dose administration).
4. Thrombocytopenia
ADULT ADMINISTRATION:
1. STEMI: Initial loading dose is 60 units/kg (max 4000 units)
2. STEMI: May continue with infusion at 12 units/kg/hr, round to nearest 50 units (maximum of 1000
units/hr for patients > 70 kg.
3. Further orders must come from medical control.
PEDIATRIC ADMINISTRATION:
Contact medical control prior to administration.
SPECIAL CONSIDERATIONS:
1. May only be administered by Critical Care Paramedics.
2. Paramedics may continue an infusion initiated at a sending facility
3. Protamine sulfate may be administered for heparin overdose/toxicity.
3-19-15
HYDROMORPHONE (DILAUDID)
ACTION:
1. Binds with opiate receptors in the CNS, altering both perception and emotional response to pain.
2. Dilaudid is 7-10 times more analgesic than morphine.
INDICATIONS:
1. Musculoskeletal trauma
2. Severe pain
CONTRAINDICATIONS:
1. Do not use in pediatric patients
2. Patients in labor
3. Respiratory depression in asthmatics, COPD.
4. Known allergies to Dilaudid (hydromorphone)
5. Patients with increased intracranial pressure.
6. Systolic BP < 90
PRECAUTION:
1. IV/IO administration should be done over 2-5 minutes
2. May be considered in patients with head or abdominal pain.
3. Use with caution in asthmatic or COPD patients presenting with respiratory difficulty.
ADVERSE REACTIONS AND SIDE EFFECTS:
1. Sedation, dizziness
2. Hypotension and bradycardia
3. Nausea or vomiting
4. Respiratory depression and bronchospasm.
ADULT ADMINISTRATION:
1. Management of pain:
a. Administer 0.5 2mg IV/IO/IM titrated to pain relief, to a max initial dose of 2mg.
b. May repeat to total dose of 4mg.
2. Monitor vital signs after each dose.
3. Contact medical control for further orders.
PEDIATRIC ADMINISTRATION:
1. For management of pain, may administer 0.5 1.0 mg IV/IO/IM or per Broselow tape to max initial dose of
1.0 mg.
2. Contact medical control for further orders.
SPECIAL NOTES:
1. May only be administered by Critical Care Paramedics.
2. Have equipment ready to assist ventilations as necessary.
3. Naloxone (narcan) may be administered for respiratory depression.
4. Dilaudid is a controlled substance, and its use must be documented according to the Controlled Substance
Policy.
3-19-15
IMIPENEM (PRIMAXIN)
ACTION:
A potent broad spectrum antibacterial agent. Bactericidal for gram negative, gram positive and anaerobic
organisms.
INDICATIONS:
Treatment of serious lower respiratory tract, urinary tract, skin and skin structure, bone and joint,
gynecological, intrabdominal, and polymicrobic infections, bacterial septicemia and endocarditis.
CONTRAINDICATIONS:
Known hypersensitivity
PRECAUTIONS:
1. Seizure potential
2. Use with caution on patients with impaired renal function
ADVERSE REACTIONS AND SIDE EFFECTS:
1. Anaphylaxis
2. Pruritus
3. Rash and urticaria
4. Abdominal pain
5. Abnormal clotting time
6. Burning at injection site
ADULT ADMINISTRATION:
1. Physician ordered dose.
2. Range from 250mg 500mg over 1 hour every 6 to 8 hours. Dose based on severity of disease,
susceptibility to pathogens, condition of patient age and weight.
3. Do not exceed 4 Gm/24hrs.
PEDIATRIC ADMINISTRATION:
1. Physician ordered dose.
2. Not recommended for pediatric patients with CNS infections because the risk of seizures.
3. Do not exceed 50mg/kg or 4 Gm/24hrs
4. Infants 15-25mg/kg dose every 6 hours
SPECIAL CONSIDERATIONS:
1. May only be administered by Critical Care Paramedics.
2. Dilute in 10 ml of compatible solution for infusion.
3. Doses greater than 500mgs should be infused over 40-60 min.
3-19-15
INSULIN
ACTION:
1. Causes uptake of glucose by the cells
2. Decreases blood glucose level
3. Promotes glucose storage
INDICATIONS:
1. Elevated blood glucose
2. Diabetic ketoacidosis
CONTRAINDCATIONS:
Avoid overcompensation of blood glucose level
PRECAUTIONS:
1. Administration of excessive dose may induce hypoglycemia. Glucose should be available
2. Conditions like puberty, pregnancy, menstruation, severe pyrexia, Infection, Psychological stress may
increase blood sugar and may increase the amount of insulin needed
ADVERSE REACTIONS AND SIDE EFFECTS:
1. Few in emergency situations
2. Redness, swelling, or itching at injection sites
ADULT ADMINISTRATION:
1. 0.1 units/kg regular insulin IV followed by an infusion at 0.1 units/kg/hr.
2. Contact medical control for further orders.
PEDIATRIC ADMINISTRATION:
Dosage is based on blood glucose level contact medical control for orders.
3-19-15
KETAMINE (KETALAR)
ACTION:
1. Causes a dissociation between the cortical and limbic system, resulting in a seemingly awake patient who is
dissociated from the environment
2. Used as a general anesthetic to prevent pain and discomfort during certain medical tests or procedures, or
minor surgery
INDICATIONS:
1. Sedation
2. RSI
CONTRAINDICATIONS:
1. Hypersensitivity
2. Significant elevation in BP
PRECAUTIONS:
Not recommended during pregnancy
ADVERSE REACTIONS AND SIDE EFFECTS:
1. Hallucinations
2. Dream like feeling
3. Nausea and vomiting
4. Excessive bronchial secretions
5. Increased skeletal muscle tone
6. Hypotension
7. Bradycardia
8. Apnea
ADULT ADMINISTRATION:
1. See Pain Management, RSI, and Sedation protocol
PEDIATRIC ADMINISTRATION:
1. 0.5 1.0 mg/kg IV/IO/IN
2. Supplemental maintenance doses are the initial dose to total dose of 4mg/kg.
3. Contact medical control for further orders.
SPECIAL CONSIDERATIONS:
1. Resuscitation equipment must be readily available
2. ECG, SPO2, ETCO2 must be in place prior to administration
3. Ketamine may be harmful to an unborn baby. Use with extreme prejudice in pregnant patients
4. Cardiac function should be continually monitored during the procedure in patients found to have
hypertension or cardiac decompensation
3-19-15
TORADOL (KETOROLAC)
ACTION:
Nonsteroidal anti-inflammatory drug (NSAID) that is indicated for the management of moderately severe,
acute pain that requires analgesia.
INDICATIONS:
1. Musculoskeletal pain
2. Abdominal pain / kidney stones
CONTRAINDICATIONS:
1. Allergy or known hypersensitivity or allergic manifestations to aspirin or other NSAIDs
2. Active peptic ulcer disease, recent GI bleeding or perforation
3. Suspected or confirmed cerebrovascular bleeding
4. Hemophilia or other bleeding problems
5. Hypotension (systolic BP < 90 systolic in adults)
6. Do not use in the second and third trimesters of pregnancy.
PRECAUTIONS:
1. Use with caution in hepatic or renal disease, CHF and asthma.
2. Use caution if the patient may need to go to surgery, Ketorolac inhibits platelet aggregation and can prolong
bleeding time for up to 48 hours.
3. Contact Medical Control Physician before giving to patients > 65 years old.
4. Carefully observe patients with defects in the blood clotting mechanism and those taking anticoagulants.
5. Use caution if patient is taking ASA or other NSAIDs on a regular basis.
6. Ketorolac lacks the sedative and anti-anxiety activity of Fentanyl, Morphine, or Versed.
ADVERSE REACTIONS AND SIDE EFFECTS:
1. Nausea and/or vomiting, gastrointestinal pain, diarrhea
2. Pain at the injection site
3. Prolonged bleeding time
4. Edema (face, fingers, lower legs, ankles and/or feet)
ADULT ADMINISTRATION:
1. Patients less than 65 years of age, administer 30 mg slow (> 15 sec.) IV/IO or, administer 60 mg IN/IM
slowly. If IM administration, vigorously massage site for 15-30 sec. to decrease local effects. Initial onset
with IV/IN use is 1-5 minutes with peak action in 1-2 hours and duration of 4-6 hours. Initial onset with IM use
is 30-60 minutes with peak action 1-2 hours and duration of 4-6 hours.
2. For adults with renal insufficiency or adults weighing <110 lbs., administer 15 mg IV or 30 mg IM.
PEDIATRIC ADMINISTRATION:
1. Administer initial dose of 15 mg IV/IO/IM.
2. Further orders must come from medical control.
SPECIAL NOTES:
1. May only be administered by Paramedic or Critical Care Paramedics.
2. Do not mix ketorolac tromethamine with morphine sulfate or promethazine in a syringe as this will result
in precipitation of ketorolac from solution.
3-19-15
LEVOFLOXACIN (LEVAQUIN)
ACTION:
Levofloxacin is an antibiotic that stops multiplication of bacteria by preventing the reproduction and repair of
their genetic material, DNA. It is in a class of antibiotics called fluoroquinolones.
INDICATIONS:
1. Nosocomial Pneumonia
2. Community-Acquired Pneumonia
3. Acute Bacterial Sinusitis
4. Acute Bacterial Exacerbation of Chronic Bronchitis
5. Complicated Skin and Skin Structure Infections
6. Chronic Bacterial Prostatitis
7. Complicated Urinary Tract Infections
CONTRAINDICATIONS:
Persons with known hypersensitivity to levofloxacin, or other quinolone antibacterials
PRECAUTIONS:
Renal Disease
ADVERSE REACTIONS AND SIDE EFFECTS:
1.
2.
3.
4.
5.
6.
Nausea
Headache
Diarrhea
Insomnia
Constipation
Dizziness
ADULT ADMINISTRATION:
3-19-15
MANNITOL (OSMITROL)
ACTION:
Mannitol increases the osmotic pressure of the glomerular filtare, thereby inhibiting reabsorption of water and
electrolytes. Causes excretion of: water, sodium, potassium, chloride, calcium, phosphorus, magnesium, urea,
and uric acid.
INDICATIONS:
1. Increased intracranial pressure
2. Toxic overdose
3. Edema
4. Crush syndrome
5. Electrical burns
CONTRAINDICATIONS:
1. Hypersensitivity
2. Anuria
3. Dehydration
4. Active intracranial bleeding
ADVERSE REACTIONS AND SIDE EFFECTS:
Confusion
Headache
Blurred vision
Chest pain
CHF
Pulmonary edema
Tachycardia
Nausea
Thirst
Vomiting
ADULT ADMINISTRATION:
1. 0.5-1.0 g/kg IV
2. Physician ordered dose
PEDIATRIC ADMINISTRATION:
3-19-15
Renal failure
Urinary retention
Dehydration
MOXIFLOXACIN (AVELOX)
ACTION:
It inhibits DNA gyrase, an enzyme required for DNA replication, transcription, repair, and recombination of
bacterial DNA. Broad spectrum bactericidal agent against both gram-positive and gram-negative organisms
INDICATIONS:
Treatment of acute bacterial sinusitis, acute bacterial exacerbation of chronic bronchitis, community acquired
pneumonia, skin and skin structure infections, bacterial conjunctivitis, and complicated skin infection
CONTRAINDICATIONS:
1. Hypersensitivity to moxifloxacin or other quinolones
2. Moderate to severe hepatic insufficiency
3. Syphilis
4. History of prolonged QT interval on EKG
5. History of acute MI, acute myocardial ischemia, ventricular arrhythmias, a-fib, bradycardia,
6. History of hypokalemia
7. Patients receiving Class IA or Class III antiarrhythmic drugs
8. Tendon pain
9. Viral infection
10. Lactation
11. Torsades de pointes
PRECAUTIONS:
1. CNS disorders
2. Cerebrovascular disease
3. Colitis, diarrhea, GI disease
4. Diabetes Mellitus
5. Seizure disorder
6. Mild or moderate heart insufficiency
7. Myasthenia gravis
8. Sunlight exposure
9. Pregnancy
ADVERSE REACTIONS:
1. CNS
a. Dizziness
b. Headache
c. Peripheral neuropathy
2. GI
a. Nausea and vomiting
b. Abdominal pain and diarrhea
c. Taste perversion
d. Abnormal liver function tests
e. Dyspepsia
3. Musculoskeletal
a. Tendon rupture.
b. Cartilage erosion
3-19-15
3-19-15
NALBUPHINE (NUBAIN)
ACTION:
1. CNS depressant
2. Decreases sensitivity to pain
3. Can also be used as a supplement to balanced anesthesia, for preoperative and postoperative analgesia, and
for obstetrical analgesia during labor and delivery.
INDICATIONS:
Moderate to severe pain
CONTRAINDICATIONS:
1. Hypersensitivity
2. Head injury
3. Undiagnosed abdominal pain
PRECAUTIONS:
1. Impaired respiratory function
2. Impaired Renal or Hepatic Function
3. Myocardial Infarction
4. Patients dependent on narcotics
5. Older patients
6. Pregnancy
ADVERSE REACTIONS:
1. Respiratory depression
2. Headache
3. Altered mental status
4. Hypertension, hypotension
5. Bradycardia
6. Tachycardia
7. Blurred vision
8. Confusion, hallucinations
9. Nausea and vomiting
10. Allergic reaction
ADULT ADMINISTRATION:
1. 10 mg IV/IO, may be repeated every 3 to 6 hours as necessary
2. The recommended single maximum dose is 20 mg, with a maximum total daily dose of 160 mg.
3. Nubain as a supplement to balance anesthesia
a. 0.3 mg/kg to 3 mg/kg intravenously to be administered over a 10 to 15 minute period with
maintenance doses of 0.25 to 0.5 mg/kg in single intravenous administrations
4. Contact medical control for further orders.
PEDIATRIC ADMINISTRATION:
Contact medical control prior to administration.
3-19-15
3-19-15
NITROPRUSSIDE (NIPRIDE)
ACTION:
Dilates both peripheral arteries and veins. This reduction in peripheral vascular resistance
results in an immediate reduction in blood pressure, usually accompanied by an increase in
heart rate.
INDICATIONS:
1. Short term, rapid reduction of BP in hypertensive crises
CONTRAINDICATIONS:
1. None when used in the management of life-threatening emergencies
2. Compensatory hypertension, as in atriovenous shunt or coarctation of aorta
3. Control of hypotension in patients with inadequate cerebral circulation
4. Lactation
PRECAUTIONS:
1. Hepatic insufficiency
2. Hypothyroidism
3. Severe renal impairment
4. Hyponatremia
5. Pregnancy
ADVERSE REACTIONS AND SIDE EFFECTS:
1. Body as a Whole: diaphoresis, apprehension, restlessness, muscle twitching, retrosternal
discomfort, thiocyanate toxicity (profound hypotension, tinnitus, blurred vision, fatigue,
metabolic acidosis, pink skin color, absence of reflexes, faint heart sounds, loss of
consciousness)
2. CV: Profound hypotension, palpitation, increase or transient lowering of pulse rate,
bradycardia, tachycardia, EKG changes
3. CNS: headache, dizziness
4. GI: Nausea and vomiting, retching, abdominal pain
ADULT ADMINISTRATION:
1. Initial 0.5mcg/kg/min via pump (usual dose: 3 mcg/kg/min-rarely need > 4 mcg/kg/min).
2. Increase rate 0.5 mcg/kg/min every 3-5 minutes
3. Blood pressure checks q 1-2 minutes
4. Max 10 mcg/kg/min (should not be maintained for more than 10 minutes)
PEDIATRIC ADMINISTRATION:
Contact medical direction, not recommended for peds.
SPECIAL CONSIDERATIONS:
1. May only be administered by Critical Care Paramedics.
2. Following reconstitution, solutions usually have faint brownish tint. If solution is highly
colored, do not use
3. Promptly wrap container with aluminum foil or other opaque material to protect from light.
4. Monitor BP constantly to titrate IV infusion rate to BP response
5. Minimize adverse effects by keeping patient supine
3-19-15
NOREPINEPHRINE (LEVOPHED)
ACTION:
Causes peripheral vasoconstriction
INDICATIONS:
1. Hypotension (systolic BP <70) not due to hypervolemia
2. Neurogenic shock
CONTRAINDICATIONS:
1. Hypotensive states due to hypervolemia
2. Avoid use in patients with peripheral or mesenteric thrombosis or in patients with severe
occlusive vascular disease
PRECAUTIONS:
1. Can be deactivated by alkaline solutions
2. Constant monitoring of blood pressure is essential
3. Extravasation can cause tissue necrosis.
ADVERSE REACTIONS:
1. Anxiety
2. Headache
3. Palpitations
4. Tachyarrhythmias
5. Reflex bradycardia
6. Myocardial ischemia
7. Pulmonary edema
8. Confusion
9. Anxiety
10. Hypertension
ADULT ADMINISTRATION:
1. Initiate at 0.05 mcg/kg/min via IV pump.
a. Increase rate 0.01-0.05 mcg/kg/min every 3-5 minutes as needed Max rate of 0.3
mcg/kg/min
2. Contact medical control for further orders or questions.
PEDIATRIC ADMINISTRATION:
0.01-0.5 mcg/kg/minute (rarely used)
SPECIAL CONSIDERATIONS:
1. May only be administered by Critical Care Paramedics.
2. Must monitor BP every 5 minutes
3. May increase myocardial oxygen demand
4. In general, hypovolemia should be corrected prior to use of pressors.
5. Effects of norepinephrine are enhanced by tricyclic antidepressants, MAO inhibitors,
antihistamines, guanethidine, egot alkaloids, and methypdopa.
6. Do not mix norepinephrine with alkaline solutions (e.g., sodium bicarbonate).
3-19-15
4
5
5
0
5
5
6
0
6
5
7
0
.01
.02
.03
2
3
5
2
4
6
2
4
6
2
5
7
2
5
7
3
5
8
.04
.05
.06
1
0
1
2
1
4
1
5
1
7
1
9
2
0
2
2
2
4
2
5
1
1
1
3
1
5
1
7
1
9
2
1
2
3
2
4
2
6
2
8
1
0
1
2
1
4
1
7
1
9
2
1
2
3
2
5
2
7
2
9
3
1
1
1
1
4
1
6
1
8
2
0
2
3
2
5
2
7
2
9
3
2
3
4
1
0
1
2
1
5
1
7
2
0
2
2
2
4
2
7
2
9
3
2
3
4
3
7
1
1
1
3
1
6
1
8
2
1
2
4
2
6
2
9
3
2
3
4
3
7
3
9
.07
.08
.09
.10
.11
.12
.13
.14
.15
3-19-15
Weight in Kilograms
7 8 8 9 9
5 0 5 0 5
Milliliters per hour
3 3 3 3 4
6 6 6 7 7
8 9 1 1 1
0 0 1
1 1 1 1 1
1 2 3 4 4
1 1 1 1 1
4 5 6 7 8
1 1 1 2 2
7 8 9 0 1
2 2 2 2 2
0 1 2 4 5
2 2 2 2 2
3 4 6 7 9
2 2 2 3 3
5 7 9 0 2
2 3 3 3 3
8 0 2 4 6
3 3 3 3 3
1 3 5 7 9
3 3 3 4 4
4 6 8 1 3
3 3 4 4 4
7 9 1 4 6
3 4 4 4 5
9 2 5 7 0
4 4 4 5 5
2 5 8 1 3
10
0
10
5
11
0
11
5
12
0
4
8
11
4
8
12
4
8
12
4
9
13
5
9
14
15
16
17
17
18
19
20
21
22
23
23
24
25
26
27
26
28
29
30
32
30
32
33
35
36
34
35
37
39
41
38
39
41
43
45
41
43
45
47
50
45
47
50
52
54
49
51
54
56
59
53
55
58
60
63
56
59
62
65
68
PANCURONIUM (PAVULON)
ACTION:
Skeletal muscle relaxant, paralyzes skeletal muscles including respiratory muscles
INDICATIONS:
1. Long term paralyzation post RSI
2. An adjunct to general anesthesia, to facilitate tracheal intubation and to provide skeletal
muscle relaxation during surgery or mechanical ventilation
CONTRAINDICATIONS:
Hypersensitivity
PRECAUTIONS:
1. Renal failure
2. Anaphylaxis
3. Hepatic and/or biliary tract disease
4. Long term use in ICU
5. Severe obesity
6. Pregnancy
ADVERSE REACTIONS AND SIDE EFFECTS:
1. Respiratory depression
2. Increased intracranial pressure
3. Wheezing
4. Arrhythmias, bradycardia, sinus arrest
5. Hypertension, hypotension
6. Increased intraocular pressure
ADULT ADMINISTRATION:
1. Initial dose 0.04 0.1 mg/kg
2. Repeat doses of 0.01 0.02 mg/kg
PEDIATRIC ADMINISTRATION:
1. Initial dose 0.04 0.1 mg/kg
2. Repeat doses of 0.01 0.02 mg/kg
SPECIAL CONSIDERATIONS:
1. May only be administered by Critical Care Paramedics.
2. Onset of action 30-45 seconds, peak 3-5 minutes. Effect may persist up to 60 minutes
3. Have equipment ready to assist ventilations as necessary
3-19-15
PANTOPRAZOLE (PROTONIX)
ACTION:
A proton pump inhibitor that suppresses the final step in gastric acid production.
INDICATIONS:
1. Short term treatment (7-10 days) of gastroesophageal reflux disease (GERD) with a history
of erosive esophagitis.
2. Maintenance of Healing of Erosive Esophagitis
3. Pathological Hypersecretory Conditions Including Zollinger-Ellison Syndrome
CONTRAINDICATIONS:
Known hypersensitivity
PRECAUTIONS:
1. Gastric malignancy may be present even though patients symptoms have subsided
2. Watch for hypersensitive reaction
3. Atrophic Gastritis
4. Bone Fracture (Pts with long term use of Medication)
5. Tumorigenicity
ADVERSE REACTIONS AND SIDE EFFECTS:
1. Headache
2. Abdominal pain
3. Chest pain
4. Dyspnea
5. Hemorrhage
6. Diarrhea
7. Nausea
8. Vomiting
9. Dizziness
10. Rash
ADULT ADMINISTRATION:
40mg IV/IO once
PEDIATRIC ADMINISTRATION:
1. Children 5 years and older (short term treatment of erosive esophagitis associated with
GERD)
a. 33 lbs. 88 lbs. 20 mg IV/IO once
b. Greater than 88 lbs. 40 mg IV/IO once
SPECIAL CONSIDERATIONS:
1. May only be administered by Critical Care Paramedics.
2. Pt should not receive Protonix if allergic to pantoprazole or to any other benzimidazole
medication such as albendazole (Albenza), or mebendazole (Vermox)
3. Protonix is not for immediate relief of heartburn syptoms
3-19-15
3-19-15
POTASSIUM CHLORIDE
ACTION:
1. Important for maintenance of body fluid composition and electrolyte balance.
2. Prevent or to treat low blood levels of potassium (hypokalemia)
INDICATIONS:
Prophylaxis or treatment of potassium deficiency. (Hypokalemia due to diuretic therapy,
adjunct to treatment of digoxin toxicity, low dietary potassium intake, vomiting diarrhea,
diabetic acidosis, metabolic alkalosis, corticosteroid therapy, increased renal excretion
resulting from acidosis, hemodialysis.)
CONTRAINDICATIONS:
1. Any disease or condition in which potassium levels increase may occur through potassium
retention or other processes.
2. Hyperkalemia
3. Renal failure
4. Complete heart block
PRECAUTIONS:
Impaired renal function or adrenal insufficiency can cause potassium intoxication, which can
develop rapidly and without symptoms.
ADVERSE REACTIONS AND SIDE EFFECTS:
1. Abdominal Pain
2. Diarrhea, Nausea Vomiting
3. Potassium Intoxication: cardiac arrest, cardiac arrhythmias, increased amplitude of T wave,
decreased amplitude of R wave, disappearing P wave, PR elongation, hypotension, altered
LOC.
4. Fever
5. Hyperkalemia
6. Hypervolemia
7. Muscle weakness
8. Venous thrombosis
9. Phlebitis
ADULT ADMINISTRATION:
1. Physician ordered dose.
2. Infusion rates should not exceed 10 mEq per hour or 120 mEq per day.
3. A liter of fluid containing 40 mEq of potassium should be administered over an 8-hour
period
PEDIATRIC ADMINISTRATION:
Physician ordered dose.
SPECIAL CONSIDERATIONS:
1. May only be administered by Paramedic or Critical Care Paramedics.
2. Concentrated potassium solutions must be diluted before administration; direct injection
can be fatal.
3. 40mEq/L is preferred dilution amount but check labels
4. Can be mixed with Sodium Chloride
3-19-15
PROCHLORPERAZINE (COMPAZINE)
ACTION:
1. Blocks dopaminergic receptors in the brain
2. Anti-psychotic medication
3. Anti-emetic
INDICATIONS:
1. Severe nausea and vomiting
2. Acute psychosis
3. Migraine headache
4. Treatment of schizophrenia
CONTRAINDICATIONS:
1. Hypersensitivity
2. Comatose patients
3. Patients that have received large amounts of CNS depressants
4. Pediatric surgery
5. Do not use in pediatric patients under 2 years of age or under 20 lbs. Do not use in children
for conditions for which dosage has not been established
PRECAUTIONS:
The antiemetic action of Compazine (prochlorperazine) may mask the signs and symptoms of
overdosage of other drugs and may obscure the diagnosis and treatment of other conditions .
ADVERSE REACTIONS AND SIDE EFFECTS:
1. Drowsiness
2. Sedation
3. Blurred vision
4. Tachycardia or bradycardia
5. Dizziness
6. Hypotension
7. Neuromuscular (Extrapyramidal) Reactions
8. Dystonias
9. Pseudo-parkinsonism
10. Tardive Dyskinesia
11. Neuroleptic Malignant Syndrome (NMS)
ADULT ADMINISTRATION:
1. 5-10mg IM or slow IV.
2. Contact medical control for further orders.
PEDIATRIC ADMINISTRATION:
Not recommended.
SPECIAL CONSIDERATIONS:
1. May only be administered by Critical Care Paramedics.
2. May potentiate the effects of narcotics, sedatives, hypnotics, and alcohol
3-19-15
PROPOFOL (DIPRIVAN)
ACTION:
1. Short-acting, intravenously administered hypnotic agent
2. Used to help you relax before and during general anesthesia for surgery or other medical
procedure
INDICATIONS:
Provide sedation to patients with controlled ventilation
CONTRAINDICATIONS:
Patients should not receive this medication if allergic to Propofol, eggs, soy products, or soy
beans
PRECAUTIONS:
1. Patients should be continuously monitored for early signs of hypotension and/or
bradycardia
2. Apnea requiring ventilatory support often occurs during induction and may persist for
more than 60 seconds
3. Medical use requires caution when administered to patients with disorders of lipid
metabolism such as primary hyperlipoproteinemia, diabetic hyperlipemia, and pancreatitis
4. When injected to a patient who is epileptic, there is a risk of seizure during the recovery
phase
ADVERSE REACTIONS AND SIDE EFFECTS:
1. Allergic reactions:
a. Hives
b. Difficulty breathing
c. Swelling of face, lips, tongue, or throat
2. Seizure
3. Respiratory
4. Fast or slow HR
5. Nausea
6. Green urine
ADULT ADMINISTRATION:
1. 5-50mcg/kg/min. If greater than 50mcg is required contact medical control. Absolute
maximum dose is 80mcg/kg/min
2. May increase 5mcg/kg/min every 5 minutes based on required sedation
3. Bolus dosing 10-20 mg IVP slowly to quickly increase depth of sedation for patients
3-19-15
RACEMIC EPINEPHRINE
ACTION:
Sympathomimetic bronchodilator. Racemic epinephrine works by stimulation of the adrenergic receptors in the airway with resultant tightening of the mucosa (mucosal
vasoconstriction) and decreased fluid in the airway (subglottic edema) and by stimulation of
the -adrenergic receptors causing relaxation of the bronchial smooth muscle.
INDICATIONS:
1. Stridor
2. Croup
3. Bronchiolitis
CONTRAINDICATIONS:
1. Hypersensitivity to drug or sulfates
2. Epiglottitis
PRECAUTIONS:
1. Use cautiously in patients with hypertension, diabetes, elderly patients and patients with
cardiac disease (angina, MI, or tachycardia)
2. Syncope may develop in asthmatic children.
ADVERSE REACTIONS AND SIDE EFFECTS:
1. Increased heart rate
2. Nausea
3. Anxiety
4. Heart palpations
5. Headache
ADULT ADMINISTRATION:
1. 0.5 0.75 ml of a 2.25% solution in 2.0 ml normal saline via nebulizer.
2. Contact medical control for additional orders.
PEDIATRIC ADMINISTRATION:
1. >4 years: 0.25 0.50 ml of a 2.25% solution in 2.0 ml normal saline via nebulizer. Contact
medical control for additional orders.
2. <4 years: Contact medical control for orders.
SPECIAL NOTES:
1. May only be administered by Paramedic or Critical Care Paramedics.
3-19-15
3-19-15
3-19-15
VANCOMYCIN (VANCOCIN)
ACTION:
A very potent tryicylic glycopeptide antibiotic, it is bactericidal against gram positive
organisms.
INDICATIONS:
1. Serious gram positive infections.
2. Penicillin allergic patients
3. Endocarditis
CONTRAINDICATIONS:
1. Known Hypersensitivity
2. Corn Products
PRECAUTIONS:
1. Prolonged use can cause super infections that are not susceptible to antibiotic treatment.
2. Kidney problems
3. Hearing problems
4. Stomach and intestinal problems
ADVERSE REACTIONS AND SIDE EFFECTS:
1. Chills
2. Dizziness
3. Fever
4. Fatigue
5. Rash/urticaria
6. Anaphylaxis
7. Flushing of the upper body
8. Easy bleeding or bruising
9. Diarrhea
10. Ringing in the ears
11. Change in the amount of urine
ADULT ADMINISTRATION:
1. Physician ordered dose.
2. 7.5mg/kg every 6 hours or 15mg/kg (1gm) every 12 hours for 7-10 days
3. Max dose: 3 4 gm/24 hrs
PEDIATRIC ADMINISTRATION:
1. Physician ordered dose.
2. 40mg/kg/24 hrs
3. Do not exceed 2 Gm in 24 hours
SPECIAL CONSIDERATIONS:
1. May only be administered by Critical Care Paramedics.
2. Drug may cause dizziness, do not drive or use machinery
3-19-15
VECURONIUM BROMIDE
ACTION:
1. Non-depolarizing neuromuscular blocking agent; onset 2-3 minutes; duration: 30-90
minutes.
2. Paralysis onset decreases and duration of maximal effect increases with increasing doses.
INDICATIONS:
1. When further muscle paralysis is necessary following RSI.
2. Intubated patients that are experiencing tube stress agitation.
3. Patients that have uncontrolled motor activity that may threaten the airway or spine.
4. For further paralysis of an interfacility patient who has already been through RSI by
hospital staff.
CONTRAINDICATIONS:
1. Hypersensitivity
2. Newborns (< 28 days)
3. Myasthenia gravis
PRECAUTION:
1. Known pregnancy
2. Must use measures to control pain and anxiety after the paralytic has been administered.
3. Sedation should be used when vecuronium has been administered unless contraindicated.
ADVERSE REACTIONS AND SIDE EFFECTS:
1. Prolonged apnea/respiratory paralysis.
2. Inability to perform adequate neurological exam.
3. Quinidine, magnesium and certain antibiotics may intensify paralysis
ADULT ADMINISTRATION:
1. Must be diluted with sterile water.
2. For paralysis:
a. Adult administration is 0.1 mg/kg IV/IO
b. May repeat dose, as indicated and necessary
3. Must provide total ventilatory support after administration
4. Contact medical control for further orders.
PEDIATRIC ADMINISTRATION:
1. Administer 0.1 mg/kg IV/IO (Refer to Broselow pediatric tape.) May repeat dose as
necessary.
2. Must provide total ventilatory support after administration
3. Contact medical control for further orders.
SPECIAL CONSIDERATIONS:
1. May only be administered by Critical Care Paramedics.
2. Not to be used for initial paralysis to obtain an airway.
3. Have equipment ready to assist ventilations as necessary.
4. Watch for hypersensitivity or allergic reaction.
5. May be useful in status asthmaticus or epilepticus.
3-19-15
3-19-15