Section 2: Medical Protocols Flashcards
(38 cards)
2.01 Acute Neurologic Event with Evidence of Increased ICP Recognition/BLS
- Patient with altered mental status (GCS <8), abnormal motor posturing, unilateral or bilateral dilation of pupils, +/- bradycardia and/or hypertension.
- Possible etiologies include traumatic brain injury, epidural hematoma, subdural hematoma, subarachnoid hemorrhage, primary intracerebral hemorrhage, tumor, or encephalopathy.
E - Routine patient care.
- If feasible, elevate the head of bed to > 30°.
- Avoid obstructions to venous drainage, such as tight cervical collars, securing devices for endotracheal tubes, or a non-midline head position.
- Provide airway management as indicated per the age appropriate Airway Management Protocol.
- Ventilate the patient to maintain an EtCO2 of 30-35 mmHg (avoid over aggressive hyperventilation), if capnography is not available, ventilate the patient at a rate of 14-16 bpm.
- Perform blood glucose analysis and manage hypoglycemia per the age appropriate Diabetic Emergencies Protocol.
- Transport the patient to the nearest appropriate Hospital Emergency Facility.
2.01 Acute Neurologic Event with Evidence of Increased ICP Treatment
- Manage hypotension per the age appropriate General Shock and Hypotension Protocol, maintain the MAP ≥ 80 or the SBP ≥ 110.
- 3% SALINE (HTS) 3 ml/kg (pediatrics 1ml/kg) IV over 15 minutes.
2.01 Acute Neurologic Event with Evidence of Increased ICP Notes
- Follow and document the patient’s neurologic examination. Convey the patient’s best neurologic examination and any episodes of hypoxia or hypotension during patient hand off.
- Attempt to obtain information related to use of antiplatelet or anticoagulants by the patient.
- Mild hyperventilation (EtCO2 30-35 mmHg) is a temporizing means of decreasing ICP and is
reserved for patients with evidence of increased ICP/brain herniation. Brain ischemia is worsened by over aggressive hyperventilation. Patients without evidence of increased ICP should be ventilated to maintain normocapnia (EtCO2 35-45 mmHg). - Short isolated episodes of hypoxia or hypotension should be avoided as they can cause secondary brain injury.
- Hyperglycemia is associated with worsened neurologic outcome. Glucose containing solutions should be administered only as indicated for the treatment of hypoglycemia.
2.02 Abdominal Pain Recognition/BLS
- Patient with complaint of abdominal pain, discomfort or cramping.
- Routine patient care.
- If the history and/or signs and symptoms are suggestive of a cardiac etiology, manage per the Chest Pain-Acute Coronary-Syndrome-STEMI Protocol.
- Manage hypotension, poor perfusion, or shock per the age appropriate General Shock and Hypotension Protocol.
- Transport the patient to the nearest appropriate Hospital Emergency Facility.
2.02 Abdominal Pain Treatment
- Acquire a multi-lead ECG in any patient ≥ 35 y.o. Manage per the Chest Pain-Acute Coronary-Syndrome-STEMI Protocol if findings suggest a cardiac etiology.
- Analgesia and antiemetic therapy as indicated per the age appropriate Patient Comfort Protocol.
2.02 Abdominal Pain Notes
- Consider a possible cardiac etiology in patients ≥ 20 y.o., diabetic patients and/or females especially with upper abdominal complaints or vague complaints of GI distress. Maintain a low threshold acquire a multi-lead ECG in these patients.
- Any female within child bearing age (12-50) should be managed as an ectopic pregnancy until such is ruled out.
- Abdominal aortic aneurysm should be considered in any patient ≥ 50 y.o. with abdominal pain, especially those with hypotension, poor perfusion, or shock.
- Mesenteric ischemia may present with severe pain with limited exam findings. Risk factors include age ≥ 60, atrial fibrillation, CHF and atherosclerosis.
2.03 Adrenal Insufficiency (AI) Recognition/BLS
- History of AI/Addison’s disease, HIV/AIDS, sepsis.
- History of long term use of steroids (asthma, COPD, rheumatoid arthritis, organ transplant), use of antifungal agents.
- Hypotension, nausea, vomiting, dehydration, abdominal pain.
- Routine patient care.
- Maintain and promote normothermia by the use of blankets and increasing the ambient temperature if possible.
- Perform blood glucose (bG) analysis and treat as indicated per the age appropriate Diabetic Emergencies Protocol.
- Manage hypotension/shock per the age appropriate General Shock and Hypotension Protocol.
- Transport the patient to the nearest appropriate Hospital Emergency Facility.
2.03 Adrenal Insufficiency (AI) Treatment
- HYDROCORTISONE 100 mg (2 mg/kg, 100 mg maximum for pediatrics) IV (preferred) or METHYLPREDNISOLONE 125 mg (2 mg/kg, 60 mg maximum for pediatrics) IV or DEXAMETHASONE 10 mg (0.3 mg/kg, 10 mg maximum for pediatrics) IV.
- Manage hypotension/shock per the age appropriate General Shock and Hypotension Protocol.
2.03 Adrenal Insufficiency (AI) Notes
- Consider AI in patients with hypotension refractory to IV fluids and or vasopressors.
- Consider administering a stress dose steroids to patients with a history of AI and any of the following: shock, fever (T>100.4°F) and ill appearing, multisystem trauma, burns (partial/full thickness) > 5% BSA, environmental hypothermia or hyperthermia, or vomiting or diarrhea with evidence of dehydration.
2.04 Adult Allergic Reaction - Anaphylaxis Recognition/BLS
- History of exposure to an antigen, e.g. bee/wasp sting, shellfish, tree nuts, latex, medication
- Itching, urticaria (hives), angioedema, wheezing, respiratory distress, chest or throat tightness, difficulty swallowing, GI symptoms, hypotension.
Mild
Flushing, urticaria, itching, erythema with normal blood pressure and perfusion
Moderate
Flushing, urticaria, itching, erythema plus respiratory (wheezing, dyspnea, hypoxia) with normal blood pressure and perfusion
Severe
+/- skin symptoms depending on perfusion. Possible itching, erythema plus respiratory (wheezing, dyspnea, hypoxia) or gastrointestinal (nausea, vomiting, abdominal pain) with hypotension and poor perfusion
- Routine patient care.
- Assess symptom severity.
- For patients with symptoms of mild severity, monitor and reassess for worsening signs and symptoms.
- For patients with symptoms of moderate severity, consider EPINEPHRINE (1:1000) 0.3 mg IM (lateral thigh) [auto-injector preferred] (avoid in patients > 50 yo or with a history of cardiac disease with mild symptoms only).
- ALBUTEROL 2.5-5 mg (+/- IPRATROPIUM) via SVN for continued wheezing (additional doses require authorization from MEDICAL CONTROL).
- For patients with severe symptoms, administer EPINEPHRINE (1:1000) 0.3 mg IM (lateral thigh) [auto-injector preferred] (for patients > 50 yo or with a history of cardiac disease, administer 0.15 mg) every 5 minutes if no improvement to maximum of 3 doses. Additional doses require authorization from MEDICAL CONTROL.
- ALBUTEROL 2.5-5 mg (+/- IPRATROPIUM) via SVN for continued wheezing (additional doses require authorization from MEDICAL CONTROL).
2.04 Adult Allergic Reaction - Anaphylaxis Treatment
- For patients with symptoms of mild severity, DIPHENYDRAMINE 50 mg PO/IV/IM and FAMOTIDINE 20-40 mg PO/IV.
- For patients with symptoms of moderate severity:
- If indicated, continue IM administration of EPINEPHRINE (maximum 3 doses).
- DIPHENHYDRAMINE 50 mg IV/IM if not already given PO.
- ALBUTEROL 2.5-5 mg (+/- IPRATROPIUM) via SVN for continued wheezing (may repeat X3).
- FAMOTADINE 20-40 mg PO/IV.
- METHYLPREDNISOLONE 125 mg IV or HYDOCORTISONE 100 mg IV or PREDNISONE 60 mg PO.
- For patients with severe symptoms:
- If indicated, continue IM administration of EPINEPHRINE (maximum 3 doses).
- NORMAL SALINE 500 ml IV bolus for a SBP <100 mmHg (may repeat to a maximum of 2L maximum).
- DIPHENHYDRAMINE 50 mg IV/IM if not already given PO.
- ALBUTEROL 2.5-5 mg (+/- IPRATROPIUM) via SVN for continued wheezing (may repeat x3).
- FAMOTIDINE 20-40 mg PO/IV.
- METHYLPREDNISOLONE 125 mg IV or HYDROCORTISONE 100 mg IV or PREDNISONE 60 mg PO.
- Consider GLUCAGON 1-4 mg IV in patients taking a beta antagonist.
- For peri-arrest hypotension refractory to IM epinephrine, push-dose EPINEPHRINE 10-20 mcg (1-2 ml EPINEPHRINE 10 mcg/ml) IV every minute followed by an EPINEPHRINE IV infusion at 5-15 mcg/minutes titrated to achieve a SBP of ≥100 or MAP ≥65.
- See NOTES for information regarding treating non-allergic angioedema with TXA
2.04 Adult Allergic Reaction - Anaphylaxis Notes
- a TXA 1000mg (1gm) IV over 10 minutes may help treat non-allergic angioedema. Angioedema may be seen in patients taking ACE inhibitors (ACE-I) [lisinopril, ramipril, captopril, benazepril, quinapril, enalapril]. ACE-I induced angioedema results from an excessive accumulation of bradykinin. This is different from the histamine mediated angioedema associated with allergic/anaphylactic reactions. The use of antihistamines, corticosteroids and epinephrine offer no benefit in ACE-I related angioedema. ACE-I induced angioedema usually starts with focal swelling (e.g., isolated swelling of the tongue or lips). Patients with severe angioedema involving the tongue with airway compromise often require nasotracheal intubation.
- The use of an auto-injector is strongly recommended for the administration of IM epinephrine at all EMS healthcare professional levels, if available.
- Recommended exam: mental status, skin, cardiac, pulmonary.
- If possible, patients with severe symptoms should remain in a supine position.
- Allergic reactions may occur with only respiratory and gastrointestinal symptoms without rash or other skin symptoms/signs.
- Patients with moderate or severe reactions should have IV access established and cardiac monitoring initiated.
- Patients > 50 yo, with a history of cardiac disease, or a heart rate > 150 are at risk for cardiac ischemia following the administration of epinephrine. These patients should have ongoing cardiac monitoring and a multi-lead ECG following the administration of epinephrine.
- In the case of hereditary angioedema (HAE), like ACE-I related angioedema, the use of antihistamines, corticosteroids and epinephrine offer no benefit. Some patients with HAE are prescribed medication which may reverse it. Paramedics may assist the patient with or administer these medication per patient or packaging/prescription instructions.
2.04 Pediatric Allergic Reaction - Anaphylaxis Recognition/BLS
- History of exposure to an antigen (e.g., bee/wasp sting, shellfish, tree nuts, latex, medication)
- Itching, urticaria (hives) angioedema, wheezing, respiratory distress, chest or throat tightness, difficulty swallowing, GI symptoms, hypotension.
Mild
Flushing, urticaria, itching, erythema with normal blood pressure and perfusion
Moderate
Flushing, urticaria, itching, erythema plus respiratory (wheezing, dyspnea, hypoxia) with normal blood pressure and perfusion
Severe
+/- skin symptoms depending on perfusion. Possible itching, erythema plus respiratory (wheezing, dyspnea, hypoxia) or gastrointestinal (nausea, vomiting, abdominal pain) with hypotension and poor perfusion
- Routine patient care.
- Assess symptom severity.
- For patients with symptoms of mild severity, monitor and reassess for worsening signs and symptoms.
- For patients with symptoms of moderate severity, consider EPINEPHRINE (1:1000) 0.15 mg for patients 15-30 kg (33-66 lbs.) or 0.3 mg for patients > 30 kg (66 lbs.) IM [lateral thigh] (auto-injector preferred).
- ALBUTEROL 2.5-5 mg (+/- IPRATROPIUM) via SVN for continued wheezing (additional doses require authorization from MEDICAL CONTROL).
- For patients with severe symptoms, administer EPINEPHRINE (1:1000) 0.15 for patients 15-30 kg (33-66 lbs. or 0.3 mg for patients > 30 kg (66 lbs.) IM [lateral] thigh (auto-injector preferred) every 5 minutes if no improvement to maximum of 3
doses. Additional doses require authorization from MEDICAL CONTROL.- ALBUTEROL 2.5-5 mg (+/- IPRATROPIUM) via SVN for continued wheezing (additional doses require authorization from MEDICAL CONTROL).
- Transport the patient to the nearest appropriate Hospital Emergency Facility.
2.04 Pediatric Allergic Reaction - Anaphylaxis Treatment
- For patients with symptoms of mild severity, DIPHENHYDRAMINE 1 mg/kg PO/IV/IM (maximum 50 mg) and FAMOTIDINE 1 mg/kg IV (maximum 40 mg).
- For patients with symptoms of moderate severity:
- If indicated, continue IM administration of EPINEPHRINE (maximum 3 doses).
- DIPHENHYDRAMINE 1 mg/kg PO/IV/IM if not already given PO (maximum 50 mg).
- ALBUTEROL 2.5-5 mg (+/- IPRATROPIUM) via SVN for continued wheezing (may repeat X3).
- METHYLPREDNISOLONE 2 mg/kg IV (maximum 60 mg) or HYDROCORTISONE 2 mg/kg IV (maximum 100 mg) or PREDNISONE/PREDNISOLONE (Orapred) 2 mg/ kg PO (maximum 60 mg).
- FAMOTIDINE 1 mg/kg IV (maximum 40 mg).
- For patients with severe symptoms:
- If indicated, continue IM administration of EPINEPHRINE (maximum 3 doses).
- NORMAL SALINE 20 ml/kg IV bolus, repeat as needed to achieve age appropriate BP (60 ml/kg maximum).
- DIPHENHYDRAMINE 1 mg/kg IV/IM if not already given PO (maximum 50 mg).
- ALBUTEROL 2.5-5 mg (+/- IPRATROPIUM) via nebulizer for continued wheezing (may repeat X3).
- METHYLPREDNISOLONE 2 mg/kg IV (maximum 60 mg) or HYDROCORTISONE 2 mg/kg IV (maximum 100 mg) or PREDNISONE/PREDNISOLONE (Orapred) 2 mg/ kg PO (maximum 60 mg).
- FAMOTIDINE 1 mg/kg IV (maximum 40 mg).
- For peri-arrest hypotension refractory to IM epinephrine, push-dose EPINEPHRINE 1 mcg/kg IV [maximum dose 20 mcg] (0.1 ml/kg EPINEPHRINE 10 mcg/ml) every 3-5 minutes followed by an EPINEPHRINE infusion at 0.01-1 mcg/ kg/minutes titrated to achieve age appropriate BP.
- See NOTES for information regarding treating non-allergic angioedema with TXA.
2.04 Pediatric Allergic Reaction - Anaphylaxis Notes
- TXA 15mg/kg (maximum 1000mg [1gm]) IV over 10 minutes may help treat non-allergic angioedema. Angioedema may be seen in patients taking ACE inhibitors (ACE-I) [lisinopril, ramipril, captopril, benazepril, quinapril, enalapril]. ACE-I induced angioedema results from an excessive accumulation of bradykinin. This is different then the histamine mediated angioedema associated with allergic/anaphylactic reactions. The use of antihistamines, corti- costeroids and epinephrine offer no benefit in ACE-I related angioedema.
- The use of an auto-injector is strongly recommended for the administration of IM epi- nephrine at all EMS healthcare professional levels, if available.
- For patients <15 kg (33 lbs.) with moderate or severe symptoms, paramedics may consider epinephrine (1:1000) 0.01 mg/kg IM.
- If possible, patients with severe symptoms should remain in a supine position.
- Allergic reactions may occur with only respiratory and gastrointestinal symptoms without a rash or other skin symptoms/signs.
- Patients with moderate or severe reactions should have IV access established and cardiac monitoring initiated.
- Tachycardia (HR >150) is common following administration of epinephrine and/or albuterol. These patients should have ongoing cardiac monitoring and should have a multi-lead ECG acquired following the administration of epinephrine.
- Do not withhold epinephrine in a normal healthy child.
- Epinephrine is the single most effective drug to reverse immediate moderate and sever symptoms and should be the first drug administered.
- Diphenhydramine helps rash and itch, steroids take time for effects to be seen.
- ACE-I induced angioedema usually starts with focal swelling (e.g. isolated swelling of the tongue or lips). Patients with severe angioedema involving the tongue with airway compromise often require nasotracheal intubation.
- In the case of hereditary angioedema (HAE), like ACE-I related angioedema, the use of anti- histamines, corticosteroids and epinephrine offer no benefit. Some patients with HAE are prescribed medication which may reverse it. Paramedics may assist the patient with or ad- minister these medication per patient or packaging/prescription instructions.
2.05 Adult & Pediatric Altered Mental Status Recognition/BLS
- Patient with reduced mental status compared with baseline.
- Routine patient care.
- Perform blood glucose (bG) analysis. If the bG is ≤ 60 mg/dl or ≥ 250 mg/dl or signs and symptoms of hypoglycemia are present in the absence of the ability to perform bG analysis, treat patient per the Diabetic Emergencies Protocol.
- Obtain history and perform initial assessment to include mental status, neurologic, head, ears, eyes, nose, throat (HEENT), skin, lungs, cardiac, abdomen, back, extremities.
- Exit to appropriate protocol as indicated based on history and assessment findings:
Suggestive Findings Protocol
Miosis, hypoventilation/apnea, needle track marks, other toxidrome findings - Toxicological Emergencies
Acetone odor on breath, rapid respiratory rate - Diabetic Emergencies
Hypotension or signs of poor perfusion - General Shock and Hypotension
Evidence of trauma, unequal pupils - Head Trauma - Traumatic Brain Injury
Hypothermia - Hypothermia andLocalized Cold Injury
Heat related illness - Heat Related Illness
2.06 Brief Resolved Unexplained Event (BRUE) Recognition/BLS
- An event occurring in an infant < 1 y.o. when the observer reports a sudden, brief (< 1 minute), and now resolved episode of ≥ 1 of the following:
- Cyanosis or pallor
- Absent, decreased or irregular breathing
- Marked change in tone (hyper or hypotonia)
- Altered level of responsiveness
- Routine patient care.
- Perform blood glucose analysis and manage per the Diabetic Emergencies Protocol.
- Obtain history of event with particular attention to:
- Activity at onset and history of the event
- State during the event (cyanosis, apnea, coughing, gagging, vomiting)
- End of the event (duration, gradual or abrupt cessation, treatment provided)
- State after the event (normal, not normal)
- Recent history (illness, injuries, sick contacts, use of OTC medications, recent immunizations, new or different formula).
- Past medical history (gestational age, pre-/perinatal history, GERD, seizures, previous BRUE).
- Family history (sudden unexplained deaths, prolonged QT interval, arrhythmias).
- Medications in the residence
- Sleeping position/parent co-sleeping.
- Transport the patient to the nearest appropriate Hospital Emergency Facility.
2.06 Brief Resolved Unexplained Event (BRUE) Notes
- BRUE was formerly known as Apparent Life Threatening Event (ALTE).
- BRUE is formally diagnosed (in the ED) only when there is no explanation for a qualifying event after conducting an appropriate history and physical examination.
- Recommended exam: general appearance, vital signs (including temperature), cardiac, pulmonary, skin, neurologic.
- BRUE is not a disease, but a symptom. Common etiologies include central apnea (immature respiratory center), obstructive apnea (structural), GERD (laryngospasm, choking, gagging), respiratory (pertussis, RSV), cardiac (CHD, arrhythmia), seizures.
- Always consider non-accidental trauma in any infant who presents with BRUE.
- Even with a normal physical examination at the time of EMS contact, patients that have experienced BRUE should be transported for further evaluation and work-up.
- It is important to note sleeping position as parent co-sleeping with child is associated with infant death.
2.07 Adult Patient Comfort Recognition/BLS
- This protocol applies to adult patients with pain or nausea and/or vomiting.
- This protocol is generally to be entered from a complaint specific protocol.
E - Assess pain severity utilizing a pain scale, circumstances, mechanism of injury, and severity of illness or injury.
- For mild to moderate pain (scale of 1-6), consider:
- IBUPROFEN 10 mg/kg (typical adult 400-800 mg) PO or,
- ACETAMINOPHEN 15 mg/kg (typical adult 500-1000 mg) PO or,
- ASPIRIN 324-650 mg PO.
- For moderate to severe pain (scale >6), consider:
- Interventions as above for mild pain.
- If available, inhaled NITRONOX (50/50 nitrous oxide and oxygen blend).
- Monitor, reassess and document response to treatment.
2.07 Adult Patient Comfort Treatment
- For mild to moderate pain (scale of 1-6) consider KETOROLAC 15 MG IV or 30 mg IM or, as an alternative to ACETAMINOPHEN above, consider ACETAMINOPHEN 500-1000 mg IV.
- For severe pain (scale >6):
- FENTANYL 0.5-1 mcg/kg IV/IM/IN [maximum single dose 50 mcg] (may repeat every 10 minutes to a maximum of 200 mcg). IV doses should be given over 2 minutes, or
- For patients with traumatic pain or burns, KETAMINE 0.1 to 0.25 mg/kg IV (may repeat x1 q 10 minutes) or 0.25 to 0.5 mg/kg IM/IN (may repeat x1 q 30 minutes).
- For patients with nausea or vomiting:
- ONDANSETRON 4 mg PO/SL/IV/IM/ODT (may repeat x1 in 15 minutes).
- For patients who do not respond to ONDANSETRON, or patients requiring electrical therapy (cardioversion or pacing) or other procedure requiring sedation, consider MIDAZOLAM 2.5-5mg IV/IM/IN or LORAZEPAM 1-2mg IV/IM or
DIAZEPAM 2.5-5 mg IV/IM or KETAMINE 0.5-1 mg/kg IV or KETAMINE 2mg/kg IM (must have continuous quantitative waveform capnography in place).
- For patients with an advanced airway in place (BIAD/ETI/cricothyrotomy) requiring sedation and analgesia, consider:
- MIDAZOLAM 2.5-5 mg IV every 5-10 minutes as needed (maximum dose 10mg) or
- LORAZEPAM 1-2 mg IV every 15 minutes as needed (maximum 10mg) and
- FENTANYL 1.0-1.5 mcg/kg slow IV push (maximum 100mcg per dose, may repeat in 10 minutes to a total of 200mcg. Contact Medical Control for additional doses).
- For patients with an advanced airway in place (ETI/BIAD/cricothyrotomy) if necessary for patient safety or to facilitate ventilation, consider ROCURONIUM 1 mg/kg IV or VECURONIUM 0.1 mg/kg IV (must have continuous quantitative waveform capnography in place and must be preceded by sedation as above).
- Monitor and reassess response to treatment and vital signs prior to and 5 minutes following any dose of narcotic analgesic and before transfer of care (patient hand off). This must be documented in the PCR.
2.07 Adult Patient Comfort Notes
- DO NOT administer ibuprofen (Motrin, Advil) or ketorolac (Toradol) to patients who are pregnant, have a history of renal failure or transplant, are allergic to non-steroidal anti-inflammatory agents (NSAIDs), have active bleeding (including GI bleeding), have suspected intracranial hemorrhage, or in patients that may require surgical intervention such as those with open fractures/fractures with deformity.
- DO NOT administer aspirin to patients that have active bleeding (including GI bleeding, suspected intracranial hemorrhage, or in patients that may require surgical intervention such as those with open fractures/ fractures with deformity).
- PO analgesics are not indicated for abdominal pain.
- DO NOT administer PO medications to patients who may require surgical intervention.
- Individual patients may respond differently to opioid analgesics. The patient’s age, weight, clinical condition, co-administered/ingested drugs (alcohol, benzodiazepines) and prior exposure to opiates should all be considered when determining the dose to be administered. Weight based dosing provides a standard means for dose calculation, but does not predict patient response. Example: minimal doses of opioids may cause respiratory depression in geriatric, opiate naïve or alcohol intoxicated patients. It is much safer to administer a low opioid dose and repeat as necessary than
to administer a high dose initially. - Avoid co-administering multiple sedating agents in non-intubated patients due to the risk for respiratory depression.
- Consider the use of waveform capnography in all patients receiving narcotic analgesics or ketamine.
- Patients with alcohol intoxication or those that have received benzodiazepines are at increased risk for respiratory depression following the administration of narcotic analgesics.
- Sub-anesthetic (low) dose ketamine has demonstrated significant analgesic efficacy without the adverse effects associated with higher doses. While uncommon, ketamine administration may result in laryngeal spasm and/or increased salivation. Laryngealspasm is transient and can be managed with positive pressure ventilation if need be.
- As the dose related effect of ketamine transitions from analgesia to anesthesia, nystagmus emerges and as such, ketamine administration should be discontinued when nystagmus occurs.
- Ketamine should be administered over 60 seconds when given IV.
- Ketamine should not be used in patients with penetrating ocular injuries or known coronary artery disease.
- Droperidol has a sedating effect. Document mental status and vital signs prior to administration.
- Advanced airway placement MUST be confirmed by the presence of waveform capnography (> 6 breaths) prior to the administration of rocuronium or vecuronium and documented continuous airway monitoring with waveform capnography is required.
- For IM administration, the 100 mg/ml concentration of ketamine is preferred.
- Ketamine in a concentration of 100 mg/ml must be diluted 1:1 with 0.9% saline, D5W or sterile water creating a 50 mg/ml concentration prior to IV use.
2.07 Pediatric Patient Comfort Recognition/BLS
- This protocol applies to pediatric patients with pain, nausea or vomiting.
- This protocol is generally to be entered from a complaint specific protocol.
E - Assess pain severity utilizing age appropriate pain scale (numeric, Wong-Baker faces or FLACC scale), circumstances, mechanism of injury, and severity of illness or injury.
- For mild to moderate pain (scale of 1-6), consider:
- IBUPROFEN 10 mg/kg (800 mg maximum) PO or
- ACETAMINOPHEN 15 mg/kg (1000 mg maximum) PO.
- For severe pain (scale >6), consider:
- Interventions as above for mild pain.
- If available, inhaled NITRONOX (50/50 nitrous oxide and oxygen blend).
- Monitor, reassess and document response to treatment.
2.07 Pediatric Patient Comfort Treatment
- For minor to moderate pain (scale of 1-6), consider KETOROLAC 0.5 mg/kg IV/IM (maximum 30 mg) or, as an alternative to ACETAMINOPHEN above, consider ACETAMINOPHEN 15 mg/kg IV (1000 mg maximum single dose).
- For severe pain (scale >6):
- FENTANYL 0.5-1 mcg/kg IV/IM/IN [maximum single dose 50mcg] (may repeat every 10 minutes to a maximum cumulative dose of 150 mcg). IV doses should be given over 2 minutes or
- For patients with traumatic pain or burns, KETAMINE 0.1 mg/kg IV or 0.2 mg/kg IM/IN. IV dosing may be repeated every 10 minutes and IM/IN doses may be repeated once in 30 minutes as needed to a maximum cumulative dose of 10 mg.
- For patients with nausea or vomiting, ONDANSETRON 0.2 mg/kg (maximum dose 4 mg) PO/SL/IV/IM/ODT (may repeat x1 in 15 minutes). Do not use in patients <3 months old.
- For patients requiring electrical therapy (cardioversion or pacing) or other
procedure requiring sedation, consider MIDAZOLAM 0.1 mg/kg [2.5 mg maximum] IV/IM/IN or FENTANYL 2 mcg/kg [50mcg maximum] IV/IM/IN or KETAMINE 0.5-1 mg/kg IV or KETAMINE 2 mg/kg IM (must have continuous quantitative waveform capnography in place). - For patients with an advanced airway in place (ETI/BIAD/cricothyrotomy) requiring sedation, consider FENTANYL 1.5-3.0 mcg/kg IV (maximum 50mcg per dose, may repeat in 10 minutes to a total of 100mcg. Contact Medical Control for additional doses).
- Monitor and reassess response to treatment and vital signs prior to and 5 minutes following any dose of narcotic analgesic and before transfer of care (patient hand off). This must be documented in the PCR.
2.07 Pediatric Patient Comfort Notes
- Use extreme caution in administering opioids to patients < 10 kg.
- DO NOT administer Ibuprofen (Motrin, Advil) and ketorolac (Toradol) to patients who are pregnant, have a history of renal failure or transplant, are allergic to non-steroidal anti- inflammatory agents (NSAIDs), have active bleeding (including GI bleeding), have suspected intracranial hemorrhage, or in patients who may require surgical intervention such as those with open fractures/fractures with deformity.
- DO NOT administer aspirin to patients that have active bleeding, including GI bleeding, have suspected intracranial hemorrhage, or in patients who may require surgical intervention such as those with open fractures / fractures with deformity.
- DO NOT administer PO medications to patients who may require surgical intervention.
- PO analgesics are not indicated for abdominal pain.
- Individual patients may respond differently to opioid analgesics. The patient’s age, weight, clinical condition, co-administered/ingested drugs (alcohol, benzodiazepines) and prior exposure to opiates should all be considered when determining the dose to be administered. Weight based dosing provides a standard means for dose calculation, but does not predict patient response. Example: minimal doses of opioids may cause respiratory depression in elderly, opiate naïve or alcohol intoxicated patients.
- Avoid co-administering multiple sedating agents in non-intubated patients due to the risk for respiratory depression.
- Consider the use of waveform capnography in all patients receiving narcotic analgesics or ketamine.
- Patients with alcohol intoxication or those who have received benzodiazepines are at increased risk for respiratory depression following the administration of narcotic analgesics.
- For pediatric administration, the 10 mg/ml concentration of ketamine is to be used.
- Sub-anesthetic (low) dose ketamine has demonstrated significant analgesic efficacy without the adverse effects associated with higher doses. While uncommon, ketamine administration may result in laryngeal spasm and/or increased salivation. Laryngeal spasm is transient and can be managed with positive pressure ventilation if need be.
- As the dose related effect of ketamine transitions from analgesia to anesthesia, nystagmus emerges and as such, ketamine administration should be discontinued when nystagmus occurs.
- Ketamine should not be used in patients with penetrating ocular injuries or known coronary artery disease.
- Vomiting without diarrhea in pediatric patients may be related to pyloric stenosis, bowel obstruction or a CNS process (bleed, tumor, increased ICP).
- Utilize age appropriate pain scoring systems (see next page). For most patients > 9 yo, the numeric (1-10) scale is appropriate. For patients 2 months-7 years, the FLACC scale may be used. The Wong-Baker-Faces scale may be used for patients > 3 y.o.
- Advanced airway placement MUST be confirmed by the presence of a waveform capnography (> 6 breaths) prior to the administration of rocuronium or vecuronium. continuous airway monitoring with waveform capnography is required.