Dr JAMES MANOS

EMERGENCY MEDICINE AND GENERAL MEDICINE TEXTS

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ADVANCED LIFE SUPPORT (ALS) AT A GLANCE (ERC)

NOTE
All the medical procedures and drug administration mentioned in this text should be done only under a senior doctor's consultancy. Some information in this text is empirical and its reliability can't be ascertained. It is suggested to search official medical articles, books and guidelines in order to ascertain the medical information & drug doses of this text.

1 DECEMBER 2009

NOTE

All the medical procedures and drug administration mentioned in this text should be done only under a senior doctor’s consultancy.

 

 

IN HOSPITAL CPR/AED ALGORITHM

 

Safety first!

 Assess for unresponsiveness:  ‘Are you Ok’?

 No response

 Ask for help and assess the patient!

Open airway (head tilt & chin lift or jaw thrust, on trauma only jaw thrust)

Breathing assessment (look, listen feel)

& simultaneously check for carotid pulse (all these for 10 sec)

 

A)    The patient breaths and has pulse:

Assess ABCDs, give oxygen, obtain IV access (keep it open with NS normal saline and also take blood for Labs), connect to monitor & take a 12 Lead ECG. Recognize & treat any abnormality. If unconscious, place on recovery position and ask for help (activate EMT Emergency medical Team / call blue code & ask for defibrillator).

 

B)    The patient has pulse, but is not breathing (apnoea):

Activate EMT Emergency medical Team / call blue code & ask for defibrillator.

Give 1 rescue breath / 5-6 sec (10 – 12 breaths/ min). Recheck pulse every 2min.

 

C)    In case the patient breaths and has pulse, place the patient on a recovery position, if unconscious and check ABCs.

D)    The patient is pulseless: activate EMT Emergency medical Team / call blue code & ask for defibrillator (standard or AED Automated External Defibrillator).

 

Start with 30 chest compressions and next give 2 rescue breaths. Resume CPR (CPR compressions : rescue breaths ratio 30:2), until AED arrives.

 

Compressions 100/min (depth 4 – 5 cm) in the middle of the chest. Ventilations 1 breath/ 5 – 6 sec or 10 – 12 breaths/ min. The duration of each ventilation is 1 sec. The tidal volume is about 500 ml/breath (6 – 7 ml/kg). Ensure full chest recoil with the compressions.

When the patient is intubated, then ventilations and compressions are performed asyncronized. 

Attach monitor/standard defibrillator/ AED. In case of an AED you will hear the message of analyzing the rhythm. During analyzing ensure that no one touches the patient! 

 

Check Rhythm on the monitor of the standard defibrillator.

A)    Shockable rhythm (VF Ventricular Fibrillation, pulseless VT ventricular Tachycardia)

1st shock:

Gel

(Place gel on the patient’s chest for the standard defibrillator)

Joules

(For a standard defibrillator Start with 120 J for biphasic defibrillator and increase until 200 J at next shocks; In case you don’t know the Joules, then start with the Joules that the device opens on ‘defibrillator’. For monophasic give 360 J). For an AED you don’t need to choose the Joules.

 

Before each shock remove oxygen supply (nasal cannulae or oxygen mask or self inflating bag) 1 meter away or close the ventilator! Ensure no one touches the patient including yourself and the person that ventilates the patient!

Next say: ‘I am going to shock on three. One, I am clear. Two, you are clear. Three, everyone is clear’! Check visually that everyone is clear!

Then defibrillate.

Paddles (1st paddle below the right clavicle, 2nd on the left axilla at the left mid-axillary line)

In case you have an AED just apply the pads on the patient’s chest.

In case of a patient with a pacemaker or an ICD (implantable cardiac defibrillator), place the defibrillator’s pads or paddles at least 12 – 15 cm away from the pacemaker or the ICD to avoid burning the myocardium! 

A few sec before and also during the defibrillation check the monitor (ensure that rhythm hasn’t changed and also that the defibrillation has commenced) 

  Resume immediately CPR for 5 cycles of 30:2 (2 min)

 

Reassess rhythm & pulse, and so on.

B)    Non – shockable rhythm (asystole, PEA Pulseless Electrical Activity). In case of an AED you will hear the message of continuing (resuming) CPR.

Resume immediately CPR for 5 cycles of 30: 2 (2 min)

Check rhythm

 

NOTES:

 

·        When AED is analyzing the rhythm and also during the defibrillation ensure that no one touches the patient (including yourself and also the person that ventilates the patient).

ACUTE CORONARY SYNDROME (ACS)

It is classified to STEMI (ST elevation Myocardial Infarction) and NSTEMI (Non ST Elevation MI)/ UA (Unstable angina). Chest pain on MI lasts usually > 15 min, but pts with DM (Diabetes Mellitus) may not have pain!

 

Unstable angina is characterized by angina of effort with increasing frequency over a few days and provoked by less exertion. ECG may be normal, however ST depression and/or Troponin release suggest high risk patient.

 

Initial therapy on ACS, after the ABCs, is MONA, but as OANM.

·        O (Oxygen): Give Oxygen nasal cannula at 1 – 4 L/min. For more severe cases give O2 with non rebreathing mask at 15 L/min. Keep SpO2 oxygen saturation > 90%.

 

·        A (ASA, Aspirin): Give aspirin 160 – 325 mg, CHEWED. CI (contraindications) are hypersensitivity to salicylates, known bleeding disorder (e.g. hemophilia), active peptic ulcer and recent GI (gastrointestinal) bleeding.

 

Assess vitals, apply cardiac monitor, obtain a 12 lead ECG, initiate a IV line of normal saline and take blood for Labs including cardiac enzymes (e.g. CK – MB) and cardiac markers (Troponin I & T), electrolytes and coagulation studies.

 

·        N (NTG , Nitroglycerine): give up to 3 NTG tablets (each tablet 0.3 – 0,4 mg) OR 3 sprays (each puff of 0.4 mg), 5 min APPART.

CI (contraindications) to NTG is SBP (systolic BP) < 90 mmHg or BP< 30 mmHg below baseline, HR < 50 or > 100, erectile drugs (Sildenafil – Viagra or Vardenafil – Levitra the last 24 h or tadafil – Cialis the last 48 h), intracranial bleeding, aortic or mitral stenosis or HOCM and also on Right Ventricular Infarction.

 

·        M (morphine) 2 – 4 mg slowly IV push. CI are hypersensitivity to it or other opiates and also signs of CNS depression (e.g. respiratory depression, decreased BP or decreased HR). Give morphine only if 3 NTG treatments fail to relieve COMPLETELY the patient’s chest pain/ discomfort.

 

Inclusion criteria for fibrinolytic therapy include:

·        ST segment elevation > 0.2 mV in 2 adjacent chest leads or > 0.1mV in 2 or more adjacent limb leads (ACLS protocol: ST elevation >_ 1 mm in >_ 2 contiguous leads).

·        New or presumably new LBBB.

·        Dominant R waves & ST depression in V1 – V3 (posterior infarction).

The above 3 signs are conclusive only with a 12 lead ECG.

·        Signs and symptoms of ACS.

·        Onset of symptoms < 12 h ago.

 

·        Exclude CI (contraindication) for thrombolytic therapy!

 

Absolute contraindications are previous haemorrhagic stroke, ischemic stroke during the last 6 months, CNS damage (and also AV malformation, aneurysm, tumour, surgery) or neoplasm, recent (within 3 weeks) major surgery, head injury or other major trauma. Also CI are active internal bleeding (not menses) or GI (gastrointestinal) bleeding within the last month, known or suspected aortic dissection, known bleeding disorder e.g. haemophilia.

·        Relative contraindications are: refractory hypertension (systolic BP> 180, diastolic BP > 110), TIA (transit ischemic attack) the last 6months, oral anticoagulation, pregnancy or < 1 week postpartum, traumatic CPR (prolonged > 10 min with evidence of thoracic trauma), non compressible vascular (especially arterial) puncture, active peptic ulcer, infective endocarditis, advanced liver disease or advanced cancer or severe renal disease and previous allergic reaction to the thrombolytic to be used. If streptokinase has been given > 4 days previously, give a different thrombolytic (because of antibodies to it). 

 

 

·        ACS: ABCs, vitals, MONA (as OANM), monitor, 12 lead ECG, establish IV access (keep it open with NS normal saline, take blood for Labs including coagulation, electrolytes, CK – MB and Troponins I &T), CXR (< 30 min).

 

STEMI ACLS algorithm (ST elevation or new or presumably new LBBB)

  

β’ blocker

ASA (aspirin)

clopidogrel

 

< _12 h from symptoms onset

 

PCI (ER/ ED emergency room/ department door to PCI goal time 90min)

or fibrinolytics (ER/ ED emergency room/ department door to fibrinodolysis goal time is 30 min).

 

Also within 24 h give ACE inhibitors or ARBs (angiotensine receptor blockers) and statins.

 

NSTEMI (ST depression or T inversion)/ high risk UA ACLS algorithm

 

 

NTG

β’ blockers

clopidogrel

UFH or LMWH

Glycoprotein IIb/IIIa (eptifibatide or tirobifan)

 

Admit to monitored bed

Assess risk

High Risk (refractory chest pain, recurrent/ persistent ST deviation, VT ventricular tachycardia, signs of cardiac failure, hemodynamic instability)

Early invasive strategy including catheterization and revascularization for shock, within 48 h of MI (Myocardial Infraction).

Also aspirin (ASA), ACE inhibitors or ARBs & statins.

 

 

Intermediate/ low risk UA (normal or non diagnostic changes on ST/ T waves) ACLS algorithm

ST depression or increased Troponins?

If Yes, go to NSTEMI/ high risk UA algorithm (above)

 

If No, admit to ED chest unit or ER monitored bed with ECG monitoring & repeated 12 lead ECG and serial cardiac markers. 

 

 NOTES

·        On chest pain/ discomfort with a non diagnostic ECG and with negative troponins, take a targeted history, establish continue monitoring, take serial 12 lead ECGs (every 3, 6 and 12 h, or sooner if indicated), check vitals frequently and repeat cardiac markers and enzymes (CK- MB and Troponins I & T). Don’t discharge if you don’t exclude ACS. 

·        On chest pain ask if pain is pleuritic (on inspiration) and also if deteriorates with patient’s movements are with palpation. However, these can’t exclude an ACS! Also patients with DM (diabetes mellitus) may have MI without chest pain. Also on these patients DKA (diabetic Ketoaxidosis) may be ought to MI (Myocardial Infraction).

 

 

PULSELESS ARREST, ALS (Advanced life support) ALGORITHM

 

For initial steps see above ‘in hospital CPR/AED’ algorithm.

 

Attach monitor/ defibrillator

 

a.      Shockable rhythm (VF, pulseless VT).

 

1st shock:

Gel

(Place gel on the patient’s chest for the standard defibrillator)

Joules

(For a standard defibrillator Start with 120 J for biphasic defibrillator and increase until 200 J at next shocks; In case you don’t know the Joules, then start with the Joules that the device opens on ‘defibrillator’. For monophasic give 360 J). For an AED you don’t need to choose the Joules.

 

Before each shock remove oxygen supply (nasal cannulae or oxygen mask or self inflating bag) 1 meter away or close the ventilator! Ensure no one touches the patient including yourself and the person that ventilates the patient!

Next say: ‘I am going to shock on three. One, I am clear. Two, you are clear. Three, everyone is clear’! Check visually that everyone is clear!

Then defibrillate.

Paddles (1st paddle below the right clavicle, 2nd on the left axilla at the left mid-axillary line)

  

In case you have an AED just apply the pads on the patient’s chest.

 

In case of a patient with a pacemaker or an ICD (implantable cardiac defibrillator), place the defibrillator’s pads or paddles at least 12 – 15 cm away from the pacemaker or the ICD to avoid burning the myocardium! 

 

A few sec before and also during the defibrillation check the monitor (ensure that rhythm hasn’t changed and also that the defibrillation has commenced) 

 

1st shock

Biphasic 120 – 200 Joule.

or Monophasic 360 J.

Resume immediately CPR for 2 min (5 cycles of 30:2 CPR)

Check monitor/rhythm

Shockable rhythm

2nd shock

Biphasic 200 Joule

or monophasic 360 J.

Immediately resume CPR for 2 min

Epinephrine (adrenaline) 1mg rapid IV/IO push

Check monitor/ rhythm

Shockable rhythm

3rd shock

Immediately resume CPR for 2 min

Amiodarone 300 mg (diluted in 20 – 30 ml D5W 5% dextrose) rapid IV/IO push

 

ACLS: Repeat amiodarone at dose of 150 mg (diluted in 20 – 30 ml D5W rapid IV/IO push 3 – 5 min after the initial dose.

4th shock

etc.

 

ΝΟΤΕS:

 

·        Give epinephrine (adrenaline) every 3 – 5 min (after alternating shocks or every 2nd loop). According to ACLS, alternative to 1st dose of adrenaline is vasopressin 40 units once (in this case give epinephrine 10 min after vasopressin).

 

·        Rotate compressors every 2 min.

 

·        Alternative to amiodarone is lidocaine 1 – 1.5 mg/kg rapid IV/IO push which may be repeated at 0.5 – 0.75 mg/kg every 5 – 10 min. Max total dose of amiodarone is 2.2 gr/ 24h. 

 

 

·        For refractory VF ventricular fibrillation with hypomagnesaemia you should give 2 gr bolus (4ml, 8 mmol) of 50% MgSO4 (magnesium sulphate) diluted in D5W (5% dextrose). For VT ventricular tachyarrhythmias with hypomagnesaemia, Torsades de pointes, AF (atrial fibrillation) and digoxin toxicity; give 2 g MgSO4 over 10min IV.

 

 

 

b.     Non shockable rhythm (asystole or PEA)

 

In case of asystole

1.      Check another lead.

2.      Check if electrodes are detached.

3.      Increase Gain and sensitivity of the monitor.

 

On asystole or PEA:

 

·        Resume CPR.

·        Perform ET (endotracheal) intubation and establish IV/IO access.

·        Give epinephrine 1mg rapid IV/IO push. Repeat every 3 – 5 min (every 2nd loop. According to ACLS, alternative to 1st dose of adrenaline is vasopressin 40 units once (in this case give epinephrine 10 min after vasopressin).

·        Also give atropine 3 mg once rapid IV push, on asystole or PEA with HR < 60.

·        On PEA ACLS suggests to give 500 ml bolus normal saline (hypovolaemia is the commonest cause of PEA). 

·        Check also reversible causes (6 Hs and 6Ts).

 

 

 TERMINATION OF ALS

Consider termination of ALS (advanced life support) if acceptable BLS (basic life support) was provided, advanced airway was placed and successfully maintained, shockable rhythms were defibrillated, IV/IO access was established, al the appropriate drugs were administered, potentially reversible causes were ruled out or corrected and the family has been updated on the probable negative outcome of continued ALS.

 

NOTES ON ARREST:

 

·        Epinephrine (adrenaline) dose is 1 ml of 1: 1000 or 10 ml of 1: 10.000 solution.

 

·        Every drug administration should be followed by 20 ml flush of normal saline and extremity elevation for 10 – 20 sec.

 

 

REVERSIBLE CAUSES OF ARREST TO RULE OUT OR CORRECT

 

Reversible causes to be excluded and corrected in arrest are the 6 Hs & 6 Ts.

The 6 Hs include Hypovolemia, Hypoxia, Hydrogen ion (acidosis), Hypo/hyperkalemia, Hypoglycemia and Hypothermia.

 

The 6 Ts include Toxins/Tablets (poisoning), Tamponade cardiac, Tension pneumothorax, Thrombosis coronary, thrombosis pulmonary and Trauma. 

 

·        Hypovolaemia causes narrow QRS tachyarrhythmia.

·        Hypoxia causes narrow QRS bradyarrhythmia.

·        Acidosis usually causes bradyarrhythmia or other arrhythmias.

·        Hyperkalemia causes very tall (tended) peaked T waves (T waves larger than R waves in > 1 lead !), 1st degree AV (atrioventricular) block, sinus bradycardia, AV blocks, flattened or absent P waves, ST depression (!), S & T waves merging, wide QRS, VT, arrest (pulseless VT, VF, asystole, PEA).

·        Hypokalemia causes QT prolongation (such as hypomagnesaemia), flat T wave, 1st degree AV block, U waves (!), ST elevation (!), variable arrhythmias, VT, arrest (pulseless VT, VF, asystole, PEA).

·        Hypoglycemia causes tachycardia (may not appear if on β’ blockers). It also may cause ST depression or AV block. It also (as well as liver failure) may cause hemiplegia and other focal neurological signs and seizures.  

·        Cardiac tamponade causes narrow QRS tachyarrhythmia or PEA.

·        Tension pneumothorax causes narrow complex tachyarrhythmia or bradyarrhythmia (because of the hypoxia) or may cause PEA.

·        Οn hypovolemia give 500 ml normal saline bolus and reassess.

·        Except trauma, suspect hypovolemia from dehydration (e.g. high fever and/or severe/ prolonged diarrhea and/or vomiting).

·        On hypoxia and acidosis ensure effective oxygenation and ventilation. Then consider on acidosis sodium bicarbonate.

·        Sodium bicarbonate is indicated in metabolic acidosis (check ABGs arterial blood gases) – e.g. on hyperkalaemia, TCAs tricyclic antidepressants, aspirin, phenobarbital, diphenydramine and cocaine) OD (overdose) and also on prolonged (>10min) arrest. Don’t give it in patients with hypercarbic acidosis.

 

Bicarbonate’s dose is 1 mEq /kg (1mMole/Kg or 1 ml/kg) of 8.4% solution IV/IO. Ventilate the patient after bicarbonate administration. Don’t give it with catecholamines (e.g. adrenaline or dopamine) at the same IV line (at least flush the line first with normal saline).

 

·        Suspect electrolyte abnormalities on history (renal failure, recent dialysis, diuretics, severe diarrhea or vomiting etc).

·        On hypothermia do only 1 defibrillation and withhold drugs until core body temperature is > 30 degrees C (86 degrees F).

·        On poisoning/ overdose consider decontamination, gastric lavage, active charcoal, whole bowel irrigation, dialysis, antidotes.

·        Tension pneumothorax is characterized by JVD (jugular vein distension – if not hypovolemic), absent breath sounds and hyper- resonance on the affected side, decreased compliance on ventilating. Late sign is contralateral tracheal shift.

·        Massive pulmonary embolism is characterized by sudden onset of  dyspnea, pleuritic (on inspiration) chest pain, cyanosis, and JVD. It may cause PEA.

·        Tension pneumothorax, cardiac tamponade and pulmonary thrombosis are obstructive causes of PEA.

 

 

ABCs ASSESSMENT

A: airway (and C spine immobilization on suspected injury): Is the airway patent and safe (e.g. the patient talks) or threatened (e.g. stridor or ‘snoring’) or obstructed? 

 

B: Breathing: RR (respiratory rate) and depth. Shallow or labored breaths? Increased breathing labor?

 

Bilateral normal thoracic expansion or not (e.g. on flail chest)?

 

Auscultation (bases and apices, check if breath sounds are bilaterally normal or decreased or absent), percussion (normal, hyper- resonant – tympanic, decreased resonance, stony), SpO2 (oxygen saturation).

 

Give Oxygen (see below).

 

C (circulation): Pulse (radial and then carotid). Weak, fast, slow, thready? Regular or irregular?

BP.

Attach monitor. 

Perform 12 lead ECG.

 

IV/IO access. keep it open with normal saline.

 

Take blood for CBC/ FBC (full/ complete blood count), biochemistry (glucose, BUN blood urea nintrogen, creatinine, LFTs liver function tests), electrolytes, coagulation studies (Platelets, PT, aPTT, D’ dimmers, INR), cardiac enzymes (e.g. CK – MB) and markers (Troponin I & T),  pregnancy test, urinalysis, amylase, lipase, toxicology (medications, illicit drugs, alcohol). Consider also TFTs (thyroid function tests) on arrhytmias.

 

On suspected hypovolemia ask type & crossmatch and ask for e.g. 4 units P-RBCs.

 

On women at reproductive age ask pregnancy test.

 

Glucose finger stick and urine dip stick.

 

Capillary refill (normal < 2 sec on 5 sec finger pulp pressure).


Skin color and temperature. Cyanosis?

 

Cardiac failure signs such as JVD (also in tension pneumothorax and cardiac tamponade and PE pulmonary embolism) , ankle edemas, lungs bases crepitations, pulsus alterans and on children liver distension).

 

Also ABGs. 

 

D: Disability: AVPU or better GCS, pupils (size and reaction to light) and abnormal body postures (stereotypical flexion if decorticate, or stereotypical extension if  decerebrate).

 

E: Expose/environment: Expose, Log Roll, check for trauma or other signs (rash, angioedema etc). Next, prevent hypothermia (with blankets).

 

 

 PRIMARY SURVEY AT A GLANCE

·        Primary survey.

·        On A (airway) we check the airway’s patency. A is also C Spine immobilization (on suspected injury). We open airway with jaw thrust or chin lift (we use jaw thrust on suspected C – spine injury), we do suction (e.g. of vomits), we place an oropharengeal airway (if the airway is endangered and also if no gag reflex) and consider a permanent airway (e.g. ET intubation). On A we also check tracheal position and also for JVD (jugular vein distension).

·        Traps on A (airway) are cribiform and face trauma and base skull fracture with ear or nose leakage of CSF, racoon eyes and Battle sign with haematoma behind the ears and also blood from the ear. In the above cases the nasal airway or the nasogastric tube may enter to the brain so its use is contraindicated!).

·        On B (breathing) we check RR (respiratory rate), chest expansion (if it is equal bilaterally, otherwise suspect e.g. flail chest), we ausculate the chest (is breathe sound bilaterally equal?), we percuss the chest (any tympany?) and take oxygen saturation (SpO2). If RR is < 10 or > 30 (in adults) and/or GCS <_ 8 we ventilate with BMV (bag mask ventilation) or intubate (we use RSI rapid sequence intubation if GCS is >3).

·        Traps on B (breathing) are vulnerable ages (on children rib fractures are rare, if they occur they indicate severe lung injury;  the elderly are vulnerable and they may also suffer from pulmonary oedema after a high fluid resuscitation (e.g. on lung contusion). 

·        On C (circulation) we check pulse (radial and carotid; Is it fast and thready?), BP, pulse pressure (SBP systolic BP – DBP diastolic BP). We obtain vascular (IV/IO) access (2 wide IV lines – grey or orange). On hypovolemia we give 500 ml NS (normal saline) or RL (Ringers - Lactated) and reassess (we may give e.g. 1 – 2 Lt fluids) and also consider early to transfuse blood (if not type available give Group O Rh negative). Fluids should be warm (39 degrees C). On children we give 20 ml/kg fluids. On no response, we repeat 20 ml/kg and if shock still remains we give 15 ml/kg packed red blood cells PRC to 10 ml/kg crystalloids or we give 10 ml/kg whole warmed blood. On hypovolaemic newborn we give10 ml/kg fluids over 5 – 10 min.

 

After IV access we also take blood for Labs (including pregnancy test on women, toxicology, coagulation and blood type and crossmatch – we ask blood units for transfusion). We also look the color and temperature of the skin (a cold clammy skin may indicate shock, however exclude low ambient temperature!), the capillary refill timer (normal is when < 2 sec, on 5 sec finger nail pressure) and LOC (level of consciousness). 

 

We also connect to a monitor, and – if indicated (e.g. heart contusion) – we take a 12 lead ECG. If there is time, we may also take ABGs to check for acidosis.

 

·        On D (disability) we check AVPU (Alert, React to voice, Reacts to pain, Unresponsive), or if there is time (and always on head trauma) we check GCS (Glasgow comma scale). We also check pupil’s size & reaction to light and also for abnormal postures of flexion (decorticate) or extension (decerebrate).

·        Traps on D (disability) are intoxicated patient, or under illicit drugs influence. On a patient with head trauma do not attribute the decreased level of consciousness on drugs or alcohol, unless you exclude head pathology (e.g. increased ICP intracranial pressure). This is also the case in general for a patient with trauma. Other traps is the lucid interval on epidural hematoma, brain’s vasoconstriction from hyperventilation and also ICP increasing with intubation (prevent it with lidocaine as premedication of RSI rapid sequence intubation, and etomidate as an anaesthetic– the last is contraindicated on hypotension – in that case stabilize the patient e.g. with fluids and perhaps with surgery).

·        Ο E (Expose, Environment) we expose the patient (from his/her clothes) and check the skin for clues (wounds, rash, belt sign etc). We also perform log roll and check the back. Next we prevent hypothermia e.g. with blankets. E is also to call Expert! 

·        Traps on E are hypothermia which complicates clotting.

·        Aids on ABCDs are ABGs (arterial blood gases), SpO2 (oxygen saturation), capnographer (CO2 detector after intubation), Foley, Levine (nasogastric tube), ECG, DPL (diagnostic peritoneal lavage) and FAST.

·        Don’t forget to check the patient’s temperature!

·        ‘TREAT FIRST WHAT KILLS FIRST’!

·        ‘TREAT AS YOU GO’!

 

·        Secondary survey is the examination from head to toes. We check pulses and also check for lacerations, edema, deformity, paleness, tenderness, crepitation, surgical (subcutaneous) emphysema, joints mobility, sensory examination, reflexes and neurological examination etc. We use X’ Rays, Doppler, CT etc.

·        The emergency needs to be transferred to the nearest APROPRIATE (trauma) medical centre/ hospital.

·        TRIAGE is based to factors such as ABCs, the available means (personnel and devices), if we have a mass destruction, the number of victims, the time and distance for definite care, the severity of the injury and the bigger chance for survival (in case of a patient with a very serious injury that is not compatible with life, or in a case of no pulse, we go on with the rest patients and ‘flag’ this patient black – or blue in some countries – i.e. expectable to die). Triage is continuing (dynamic).

·        We do not forget log roll.

·        On secondary survey always we ask AMPLE (Allergy, Medication, Past medical history, Last meal and Environment/Events), however many prefer to ask it from the very first.

 

 

OXYGEN ADMINISTRATION

On patients WITHOUT significant hypoxia (SpO2 Oxygen saturation) and WITH ADEQUATE breathing give oxygen with nasal cannula 2 – 4 L/min.

 

On patients WITH significant hypoxia but ADEQUATE breathing give O2 (oxygen) with non rebreathing face mask with reservoir bag and flow 15 L/min.

 

In case of INADEQUATE breathing or APNEA perform BMV bag mask ventilation with self inflating bag with reservoir and oxygen supply and flow 15 L/min.

 

Keep always SpO2 oxygen saturation > 90%.

 

 

 

 

STROKE ACLS ALGORITHM

 

 Possibility for stroke

1)     Confusion, decreased LOC (Level of consciousness).

2)     Cincinnati Prehospital Stroke Scale:

1 of the following suggests possibility for stroke:

a)     Facial droop (‘smile’)

b)     Arm drift (‘raise both arms with your eyes CLOSED’)

c)     Speech (slurred, mute, inappropriate words, dysarthria).

3)     Symptoms NOT improving spontaneously (differential diagnosis with TIA transit ischemic attack).

The above criteria are also criteria for fibrinolytic therapy (alteplase rTPA)

Plus

Intracranial hemorrhage ruled out with head CT.

 

·        ABCDs. Give oxygen. Initiate IV line of normal saline NS. Perform ECG. Transport/ transfer patient for definite care (stroke unit).

·        Perform a non contrast CT. Don’t give any drug before the CT.

·        CT initially may not show ischemic stroke.

·        On Lab tests don’t forget to ask for glucose and also coagulation studies. However, do as soon as possible a glucose finger stick test to exclude hypoglycemia which may mimic stroke.

·        Don’t give D5W (5%dextrose) on stroke! Give normal saline NS.

·        The goal time for fibrinodolysis is < 3 h from symptoms onset and < 60min from ER – ED (emergency room/ department) arrival (door to treatment time).

·        Fibrinolytic therapy has as complication about 6% brain hemorrhage.

·        Do not decrease the BP fast. Call Expert.

·        Correct glucose if high or low (with symptoms).

·        Correct electrolytes.

·        Treat cardiac dysrhythmias if unstable, but don’t treat immediately AF (atrial fibrillation). Call an expert.

·        Check CI (contraindications) for thrombolysis e.g. a SBP > 185 or a DBP> 110 are CI.

 

 

LARYNGEAL MASK

It has many advantages.

We put it with normal saline, not gel. We place it holding it as a pen (with our index and thumb), until we feel resistance (our index finger enters completely in the mouth following the tongue’s rout. On the end of the tongue’s rout we may enter the tube a little bit more with the fingers of our other hand). Then we inflate the cuff. We remove it inflated!

Size is for women and small men 3 – 4 (usually 4), and for men 4 – 5 (usually 5). We inflate the cuff with tube’s size x 10 – 10 e.g. for tube size 4 we inflate with 4 x 10 – 10 = 30 ml air.

 

 

ET (ENDOTRACHEAL) INTUBATION

On adults we use curved blade size 3 or 4. Initially we preoxygenate the patient for 2 – 3 min. We assemble the equipment (ET endotracheal tube, syringe, gel, laryngoscope, SUCTION, exhaled CO2 detector, Magill’s forceps) and we insure that the light of the laryngoscope is OK and that the cuff inflates. We insert the laryngoscope at the right angle of the mouth, holding it with our left hand, and visualize the vocal cords. We don’t flex our wrist during laryngoscopy. Then, we insert the ET (which we have been lubricated with gel). We inflate the cuff with 5 – 10 cc air (usually 8 – 10cc). We ausculate both lungs (axillae) and epigastrium (ensuring bilateral normal breath sounds and absence of gastric bubbles, if breath sounds are less on the left we deflate the cuff, withdraw a few cm the tube, inflate the cuff and recheck) and attach an end tidal CO2 (carbon dioxide) detector (capnographer or oesophagal detector). Then we secure the tube and ventilate. When we extubate, we do not forget to deflate the cuff. 

 

The insertion depth of the ET is about 22 cm on women and 24 cm on men.

 

The size of ET tube on adults is 8 – 9 mmID on men and 7 – 8 mmID on women.

 

Nover forget to deflate the cuff before extubating.

 

In case you have another rescuer, you can perform Sellick maneuver during intubation, in order to prevent aspiration. However, if aspiration occurs release the Sellick maneuver, otherwise you may cause oesophagal perforation. In that case turn the patient on his/her size and perform suction. 

 

The duration of intubation is 1 breath holding (30 sec). In case this time lapses and we haven’t intubated, we stop intubation and continue BMV. 

 

The positive pressure ventilations rate is 10 – 12 breaths /min or 1 breath every 5 – 6 sec with BMV (bag mask ventilation). The duration of each ventilation is 1 sec. The tidal volume is about 500 ml/breath (6 – 7 ml/kg).

 

Alternative device for detecting correct tube placement is the oesophagal detector. However the safest method is a CXR (chest X’ Ray) where we see the ET just above the level of the carina. 

 

 

ITD DEVICE

 

ITD device is Impendence Threshold Device. It attaches to the self inflating bag mask or the tracheal tube. It let the patient to exhale if spontaneous breathing returns. It also does not permit the equalization of negative intra-thoracic pressure in case of hyperventilation. When we use it with BMV (bag mask ventilation), two rescues need to perform ventilation. When we open the ITD it has lights that open 10 times/min. During each light we ventilate.

 

 

FOREIGN BODY AIRWAY OBSTRUCTION ACLS ALGORITHM

 

a. The patient is conscious.

·        On a patient that chokes from a foreign body:

 

1.      If the patient is conscious and the cough is effective, we encourage the patient to cough.

 

2.      If the patient is conscious and the cough isn’t effective we give with our palm (thenar) 5 back blows between the patient’s scapulae & 5 abdominal thrusts (Heimlich maneuver). On pregnant and obese patients we give chest thrusts and not abdominal.

 

 

We reassess. We open the patient’s airway and remove any visible object (or use suction, if available).

 

If still not adequate breathing, we call for help.

 

b. The patients is unconscious

 

 Safety first

Check for unresponsiveness. ‘Are you OK’?

 

No response

 

Call blue code and ask a defibrillator

Open airway

Remove any visible object (or perform suction, if available)

Check for breathing (look, listen feel, 10 sec)

No breathing

Give 2 ventilations

Unsuccessful

Reposition the patients head (increase the extension) and ventilate again

 

Unsuccessful

Give 30 chest compressions

Check mouth for foreign body and remove it if visible

 

Unsuccessful

Visualize vocal cords with a laryngoscope and remove the foreign object with a Magill’s forceps.

 

 

 

WHAT TO CHECK ON MONITOR/ ECG

1.      Is there electrical activity and recognizable QRS?

2.      Which is the ventricular rhythm? It is 300/ large squares between RR waves.

3.      Are the QRS regular? If not, exclude e.g. AF (atrial fibrillation) or ectasystoles.

4.      Which is the QRS width? If > 0.12 sec (3 small squares) it is wide. Then exclude ventricular arrhythmia or BBB (bandle branch block).

5.      Is there atrial activity? Check for P waves on II and V1 leads. If not exclude e.g. AF.

6.      Which is the relationship between atrial and ventricular activity? Is it 1:1 each P followed by QRS) as normal, or is it variable (e.g. atrial flutter) or there is no relationship (e.g. AF)?

 

 

UNSTABLE WIDE COMPLEX TACHYCARDIA ALGORITHM

Generally, we treat wide complex tachycardia as VT, as it is far likely the rhythm that occurs on a wide complex tachycardia.

 

AN UNSTABLE wide complex tachycardia is characterized by one or more of the following: decreased LOC (level of consciousness), SBP (systolic BP) <90 mmHg, chest pain, heart failure, dyspnea, shock, AMI (acute MI myocardial infraction), pulmonary edema.

 

UNSTABLE WIDE COMPLEX TACHYCARDIA ALGORITHM

·        We give supplemental oxygen.

·        We connect to monitor (we put it to II lead).

·        We place IV/IO access, take blood for Labs and keep it open with normal saline.

·        We have suction and intubation equipment available

·        We take a 12 lead ECG

 

We open the monitor on II lead. Wide complex tachycardia. The patient is unstable (see above).

In case the patient isn’t unconscious you need to sedate with

1.      Midazolam 1 – 2.5 mg slowly IV

 OR

2.      Diazepam 5 – 10 mg slowly IV. 

We ensure nobody touches the patient!

 

We push the ‘synchronized’ (‘synch’) button on the defibrillator. If we don’t do it, we may cause R on T phenomenon and cause a VF! (I personally, in order not to forget to remove oxygen and push synchronized button, I say ‘Jel – O (oxygen) – Joule – synch – paddles’. Other push again ‘synch’ button after each cardioversion, however, don’t forget to perform asynchronized defibrillation shock on a shockable arrest – pulseless VT or VF).

 

 

On synchronized mode we see on the monitor arrows above the R waves.

 

Jell – Joule – paddles:

 

We put Jell on the patient’s chest

We remove oxygen supply 1 meter away (or close the ventilator)!!!

 

In case of a patient with a pacemaker or an ICD (implantable cardiac defibrillator), place the defibrillator’s pads or paddles at least 12 – 15 cm away from the pacemaker or the ICD to avoid burning the myocardium! 

 

We choose Joules (from ‘lead’ we go to ‘defibrillation’ and choose Joules).

 

We push the synch button!!!

 

We say ‘I am about to shock on 3. One, I am clear. Two, you are clear. Three, we are all clear’.

 

Check that everyone is clear, no one touches the patient (including you and the person providing ventilations, and ensure that oxygen is removed. A few sec before and during defibrillation look on the monitor and ensure that the rhythm hasn’t changed and also that the defibrillation has commenced. 

 

 

For a monophasic defibrillator (old), for monomorhpic VT we start with 100 J (next subsequent shocks are with increasing Joules: 200, 300 & 360 J). Monomorphic VT is characterized by QRS all of same size, shape and direction. For polymorphic we give 360 Joule defibrillation. Polymorphic VT is characterized by QRS of varying shape, size and direction and one form of this rhythm is Torsades de pointes.

 

For a biphasic defibrillator, for a monomorphic VT we start with 75 J and continue next shocks with 120, 150 and 200J. For a polymorphic VT we start with 120J and continue the next shock with 200J.

 

The above Joules are not indicative. Check each device’s manual for the specific Joule of defibrillation or cardioversion.

 

We place the paddles (1st paddle below the right clavicle, 2nd on the left axilla at the left mid-axillary line)

 

After the 1st cardioversion we check monitor and pulse (we check pulse to exclude PEA).

 

If needed (the arrhythmia hasn’t cardioverted) we follow with 2nd shock with the same pattern, but we just increase the Joules e.g. if the 1st shock was with 75 J, and was unsuccessful, we repeat the shock with 120J. If needed (the arrhythmia hasn’t cardioverted) we give a 3rd shock (increasing the Joules as mentioned before).

  

After the 3rd shock we administer amiodarone 300 mg IV/IO (diluted in D5W 5% dextrose) over 10 – 20 min. If needed (the arrhythmia hasn’t cardioverted) we repeat the shock (4th). Next we administer 900mg amiodarone IV/IO over 24 h. Max total dose of amiodarone is 2.2 gr/ 24h. 

 

 

 

 

 

STABLE WIDE COMPLEX TACHYCARDIA

·        We give supplemental oxygen.

·        We connect to monitor (we put it to II lead).

·        We place IV/IO access, take blood for Labs and keep it open with normal saline.

·        We have suction and intubation equipment available.

·        We take a 12 lead ECG

Generally, we treat wide complex tachycardia as VT, as it is far likely the rhythm that occurs on a wide complex tachycardia.

 

 

A)    REGULAR Broad complex stable tachycardia of unknown rhythm: amiodarone 300 mg IV push over 20 – 60 min (diluted in D5W 5% dextrose). Repeat it at 900 mg over 24 h. Max dose of amiodarone is 2.2 gr IV / 24h.

 

According to ACLS, alternatives to amiodarone are:

1.      Lidocaine 1 – 1.5 mg/kg rapid IV/IO push which may be repeated at 0.5 – 0.75 mg/kg every 5 – 10 min. Max dose is 3 mg/kg. 

 

2.      Procainamide 20 mg/min IV INFUSION until ONE of the following occurs:

a)     The arrhythmia is converted.

b)     Hypotension occurs.

c)     QT interval prolongs (increases) or QRS widens by > 50% of its pre – treatment width.

d)     Max dose of 17 mg/kg.

 

 

B)    IRREGULAR WIDE COMPLEX TACHYCARDIA

 

a.      Polymorphic VT (QRS have varying size, shape and direction):

 

i.                    According to ACLS, in case of a polymorphic VT with a normal QT interval:

·        Treat ischemia.

·        Correct electrolytes.

·        Give amiodarone 150 mg IV push diluted to D5W (5% dextrose), over 10 min OR

 Lidocaine 1 – 1.5 mg/kg IV push.

 

ii.                  If prolonged QT interval or VT with hypomagnesaemia: 

 

·        Correct electrolyte abnormalities and especially hypo/hyperkalemia or hypomagnesaemia.

·        For VT ventricular tachyarrhythmias with hypomagnesaemia, Torsades de pointes, (and also in AF atrial fibrillation and digoxin toxicity); give 2 g MgSO4 (magnesium sulphate) diluted to D5W (5% dextrose), over 10min IV.

·        ACLS: also consider overdriving pacing.

 

 

b.     Pre – excited tachycardia e.g. on WPW syndrome:

Call Expert! For pre – excited tachycardia (WPW) all antiarrhythmics are contraindicated (especially adenosine, digoxin, Calcium channel blockers and β’ blockers) because they may induce VT! Consider administrating amiodarone (150 mg IV diluted to 20 – 30 ml D5W 5% dextrose, over 10min) or (ACLS) procainamide (20 mg/min).

 

c.      AF with BBB (Bundle Bunch Block):

Treat as for a narrow complex tachycardia.

 

 

 

NOTE

·        Don’t combine antiarrhythmics that both prolong the QT (e.g. amiodarone and procainamide), because they may induce polymorphic VT and especially Torsades.

 

 

 

ANTIARRHYTHMIC MAINTENANCE INFUSION AFTER THE TERMINATION OF A WIDE COMPLEX TACHYCARDIA

In case a wide complex tachycardia was terminated pharmacologically, start a maintenance infusion of the antiarrhythmic that you used for the chemical cardioversion (e.g. amiodarone or lidocaine or procainamide). 

In case a synchronized cardioversion was used to terminate a wide complex tachycardia and an antiarrhythmic wasn’t administered, give a bolus of an antiarrhythmic and start a maintenance infusion. The infusion prevents the recurrence of the wide complex tachycardia.

 

1.      According to ACLS:

 

a.      Amiodarone maintenance infusion: 360 mg IV infusion the first 6 h (1 mg/min) and next 540 mg IV infusion the remaining 18 h (0.5 mg/ min). Max total dose of amiodarone is 2.2 gr/ 24h. 

 

b.     Lidocaine maintenance infusion: 1 – 4 mg/min titrated to desired effect.

 

c.      Procainamide maintenance infusion: 1 – 4 mg/min titrated to desired effect.

 

NOTE: each drug has contraindications e.g. don’t give amiodarone on a patient with bradycardia and hypotension, but stabilize first the patient.

 

 

2.      ACCORDING TO ALS (ERC) the loading dose of amiodarone on a wide complex tachycardia is 300 mg IV/IO diluted to D5W (5% dextrose), over 10 – 20 min for an unstable wide or narrow complex tachycardia (after the 3rd shock) or over 20 – 60 min at a stable wide complex tachycardia or an irregular stable narrow complex tachycardia; and then the maintenance dose in all the above cases is 900 mg over 24 h. Max total dose of amiodarone is 2.2 gr/ 24h. 

 

 

 

 

UNSTABLE NARROW COMPLEX TACHYCARDIA

 

AN UNSTABLE narrow complex tachycardia is characterized by one or more of the following: decreased LOC (level of consciousness), SBP (systolic BP) <90 mmHg, chest pain, heart failure, dyspnea, shock, AMI (acute MI myocardial infraction), pulmonary edema.

 

UNSTABLE NARROW COMPLEX TACHYCARDIA ALGORITHM

·        We give supplemental oxygen.

·        We connect to monitor (we put it to II lead).

·        We place IV/IO access, take blood for Labs and keep it open with normal saline.

·        We have suction and intubation equipment available.

·        We take a 12 lead ECG

 

We open the monitor on II lead. Narrow complex tachycardia. The patient is unstable (see above).

In case the patient isn’t unconscious you need to sedate with

1.      Midazolam 1 – 2.5 mg slowly IV

 OR

2.      Diazepam 5 – 10 mg slowly IV. 

 

We ensure nobody touches the patient.

We push the ‘synchronized’ (‘synch’) button on the defibrillator. If we don’t do it, we may cause R on T phenomenon and cause a VF! I personally, in order not to forget to remove oxygen and push synchronized button, I say ‘Jel – O (oxygen) – Joule – synch – paddles’. Other push again ‘synch’ button after each cardioversion, however, don’t forget to perform asynchronized defibrillation shock on a shockable arrest (pulseless VT, VF).

 

On synchronized mode we see on the monitor arrows above the R waves.

 

Jell – Joule – paddles:

 

We put Jell on the patient’s chest

 

We remove oxygen supply 1 meter away (or close the ventilator)!!!

 

In case of a patient with a pacemaker or an ICD (implantable cardiac defibrillator), place the defibrillator’s pads or paddles at least 12 – 15 cm away from the pacemaker or the ICD to avoid burning the myocardium! 

 

We choose Joules (from ‘lead’ we go to ‘defibrillation’ and choose Joules).

 

We push the synch button!!!

 

We say ‘I am about to shock on 3. One, I am clear. Two, you are clear. Three, we are all clear’.

 

Check that everyone is clear, no one touches the patient (including you and the person providing ventilations, and ensure that oxygen is removed. A few sec before and during defibrillation look on the monitor and ensure that the rhythm hasn’t changed and also that the defibrillation has commenced. 

 

For a monophasic defibrillator (old), we give initially for AF (atrial fibrillation) 100 J. If unsuccessful, we repeat at 200, 300 and 360 J respectively. For atrial flutter or PSVT (paroxysmal supraventricular tachycardia) we start with 50 Joule and, if unsuccessful, we repeat at 100, 200, 300 and 360 J respectively.

 

For a biphasic defibrillator, for PSVT, AF or atrial flutter we start with 30 J and, if unsuccessful, we repeat with 50, 75 and 120J, respectively.

 

The above Joules are not indicative. Check each device’s manual for the specific Joule of defibrillation or cardioversion.

 

We place the paddles (1st paddle below the right clavicle, 2nd on the left axilla at the left mid-axillary line)

 

After the 1st cardioversion we check monitor and pulse (we check pulse to exclude PEA).

 

If needed (the arrhythmia hasn’t cardioverted) we follow with 2nd  shock with the same pattern, but we just increase the Joules e.g. if the 1st shock was with 75 J, and was unsuccessful, we repeat the shock with 120J. If needed (the arrhythmia hasn’t cardioverted) we give a 3rd shock (increasing the Joules as mentioned before).

After the 3rd shock we administer amiodarone 300 mg IV/IO (diluted in D5W 5% dextrose) over 10 – 20 min. If needed (the arrhythmia hasn’t cardioverted) we repeat the shock (4th). Next we administer 900mg amiodarone IV/IO over 24 h. Max total dose of amiodarone is 2.2 gr/ 24h. 

 

 

 

 

STABLE NARROW COMPLEX TACHYCARDIA

·        We give supplemental oxygen.

·        We connect to monitor (we put it to II lead).

·        We place IV/IO access, take blood for Labs and keep it open with normal saline.

·        We have suction and intubation equipment available.

·        We take a 12 lead ECG

We open the monitor on II lead.

 

A.     REGULAR STABLE NARROW COMPLEX TACHYCARDIA:

 

We perform vagal maneuvers such as Valsava maneuver (we ask the patient to blow the outlet of a syringe in order to expel the plunger) or perform ipsilateral carotid sinus massage (for 5 sec, contraindicated if carotid bruits or known carotid stenosis), or placed a cold ice pack on the face (not immediately up on the skin, but on a towel) (however prefer the above 2 methods on adults).

 

If unsuccessful we give adenosine 6 mg rapid IV push (over 1 – 3 sec). If unsuccessful, we repeat after 1 – 2 min at 12mg. If still unsuccessful, we repeat after 1 – 2 min at 12 mg (to total dose of 30 mg). Each dose should be followed by 20 cc saline flush and arm elevation for 10 – 20 sec. The injection should be performed on a close to heart vein (e.g. antecubital fossa).

 

1.      If rhythm hasn’t converted, we call Expert! The rhythm may be probable atrial flutter. In that case control rate, e.g. with β’ blockers.

 

2.      If normal sinus rhythm is restored, the previous rhythm was probable PSVT (Paroxysmal Supra – Ventricular Tachycardia): we monitor ECG. If it recurs we administer again adenosine and consider antiarrhytmic prophylaxis, such as Calcium channel blockers.

 

Calcium channel blockers Indications are: control of ventricular rate in AF atrial fibrillation and atrial flutter (consider anticoagulation!). Also, for stable narrow complex tachycardia that is not terminated by vagal manoeuvres or adenosine. Also, verapamil is used in ectopic atrial tachycardias.

 

Verapamil 2.5 – 5 mg IV over 2 min. It may be repeated 15 – 30min later at 5 – 10 mg, to a max dose of 20 mg. 

Alternative is

 

Diltiazem 15 – 20 mg (0.25 mg/kg) IV over 2 min. It may be repeated after 15 min at 20 – 25 mg (0.35 mg/kg) over 2 min. Maintenance dose is 5 – 15 mg/h titrated to HR and BP.

 

To control ventricular rate in patients with AF (atrial fibrillation) or atrial flutter (usually when the arrhythmia is < 48h) give Diltiazem 15 – 20mg IV over 2 min.

 

CI (contraindications) to calcium blockers are wide complex tachycardia of uncertain origin, poison or drug induced tachycardia, pre – excited tachycardia e.g. rapid atrial flutter or AF in patients with WPW, SN sinus nodus disease, AV (atrioventricular) block without pacemaker, and perhaps on CHF (congestive heart failure), because of negative inotropic action (especially of verapamil). Give them with caution if LV (left ventricular) dysfunction. Use sustained long acting formula, because short acting increase the risk for ACS/ MI (acute coronary syndrome/ myocardial infarction)!

 

Verapamil is a negative inotropic agent so avoid it in patients with left ventricular impairment or heart failure, even they are stable! Also, avoid it on 2nd or 3rd degree heart block, sick sinus syndrome.

 

Don’t give concomitantly a Calcium blocker with a β’ blocker, because they may cause severe hypotension and bradycardia.  

 

 

B.    IRREGULAR STABLE NARROW COMPLEX TACHYCARDIA:

 

It is probable AF (Atrial Fibrillation). Call expert. The expert will deside also if coagulation will be administered in high risk patients < 48h or on patients > 48 h from AF onset (an ECHO may be needed to exclude intracardial thrombus that may cause stroke). 

 

Control rate with β’ blocker or digoxin IV.

 

a.      β’ blockers:

 

βblockers are indicated for narrow complex regular tachycardia uncontrolled by vagal maneuvers and adenosine on patient with preserved ventricular function. Also to control rate in AF (atrial fibrillation) and atrial flutter with duration < 48h and with preserved the ventricular function (don’t give it in rapid ventricular rate caused by accessory pathway in pre-excited arrhythmias such as WPW). 

 

Atenolol (β1) 5mg over 5 min. May be repeated 10 min later at same dose.

 

Metoprolol (β1) 2 – 5 mg slow IV at 5 min intervals. Total dose 15mg.

 

Propanolol (β1&β2) 100 mcg (μg) (=0.1 mg)/kg in 3 divided doses at 2 min intervals. It is usually used in hyperthyroidism (there exclude AF atrial fibrillation!).

 

Esmolol (β1 short acting!) 500 mcg (μg) (=0.5mg)/kg over 1 min followed by infusion of 50 – 200 mcg/kg/min.

 

CI (contraindications) to β’ blockers are: heart failure (IV category), bronchospasm/ COPD (with bronchospasm), asthma, AV block/ bradycardia and brittle insulin depended DM (IDDM).

 

Don’t give concomitantly a Calcium blocker with a β’ blocker, because they may cause severe hypotension and bradycardia.  

  

b.     Digoxin:

 

Digoxin’s dose for AF (atrial fibrillation) or atrial flutter with fast ventricular response is 500 mcg (=0.5 mg) IV over 30 min.

 

Contraindications to digoxin are: VF, VT, HR < 60 bpm and pre – excited tachycardia e.g. WPW. Use with caution in renal failure

 

 

·        If onset is < 48 h consider amiodarone 300 mg IV/IO over 20 – 60 min (diluted in D5W 5% dextrose). Then give maintenance dose 900mg IV over 24 h. Max total dose of amiodarone is 2.2 gr/ 24h. 

 

·        If rhythm hasn’t converted, we call Expert! The rhythm may be probable atrial flutter. In that case control rate e.g. with β’ blockers.

 

NOTE

High risk patients and patients with AF> 48 h may need anticoagulation before chemical or electrical cardioversion (unless a cardiac Echo excludes intra-cardial thrombus). 

 

 

 

NOTE FOR AMIODARONE

Indications of amiodarone are VF ventricular fibrillation and pulseless VT ventricular tachycardia (refractory to defibrillation), polymorphic VT ventricular tachycardia, wide complex tachycardia of uncertain origin, stable VT (when cardioversion is unsuccessful), as an adjunct to synchronized cardioversion in SVT supraventricular tachycardia, termination of ectopic atrial tachycardia, rate control in AF atrial fibrillation and atrial flutter resistant to other therapies. Also used in pre-excitation tachycardia e.g. in WPW. 

 

CI (contraindications) to amiodarone are known sensitivity, SN (sinus node) disease with severe bradycardia, and 2nd or 3rd degree AV atrioventricular block.

 

 

 

UNSTABLE BRADYCARDIA

Adverse signs on bradycardia are SBP (systolic BP)<90, HR<40, heart failure, ventricular arrhythmias compromising BP.

 

Risk factors for asystole are recent asystole, type II (Mobitz II) 2nd degree AV (atrioventricular) block, complete heart block with broad QRS and ventricular pauses > 3 sec. In the above factors perform TCP (Transcutaneous Pacing) a.s.a.p (as soon as possible). TCP is also indicated on denervated (e.g. transplanted) heart where drugs will not work.

 

Relative bradycardia is the phenomenon where HR is faster than the one that would expected for the patient’s condition. For example a patient with HR 65 bpm and BP 80/ 50 has relative bradycardia because HR is too slow, relative to (regarding to) the BP.

 

 

ALGORITHM FOR UNSTABLE BRADYCARDIA:

·        Administer oxygen.

·        Put on monitor. Chose II lead.

·        Establish IV/IO access, initiate normal saline to keep open and take blood for labs. Check especially the electrolytes.

·        Take a 12 lead ECG.

 

a.      ΟΝ ADVERSE SIGNS (see above):

·        Give atropine 0.5 mg rapid IV push. Repeat every 3 – 5 min to max 3 mg.

 

On satisfactory response to atropine check if there is risk for asystole (see above).

 

 

b.     IF NO SATISFACTORY RESPONSE ON ATROPINE OR ON RISK OF ASYSTOLE (see above):

·        Initiate epinephrine (adrenaline) infusion at 2 – 10 mcg/min.

 

Alternative to adrenaline is dopamine infusion at 2 – 10 mcg/kg/min. Consider 500ml NS normal saline bolus before dopamine. Other alternative drugs include aminophylline, isoprenaline (better avoid it, as it may be arrhytmogenic), glucagon (used on β’ blocker or Calcium channel blocker OD overdose).

 

·        Seek expert help and arrange transvenous pacing.

 

 

NOTES

·        If no immediately available TCP, we give drugs.

·        Glycopyrronium may be used instead of atropine.

·        To differentiate complete AV block from idioventricular rhythm  we increase the GAIN of the defibrillator to check for P waves (no P waves on idioventricular rhythm, but on complete AV block there is dissociation between P and QRS).

 

 

 

 TCP (TRANSCUTANEOUS PACING):

 Indications are:

1.      Symptomatic bradycardia with signs and symptoms related to it, when atropine is unavailable or unsuccessful.

2.      2nd degree type II (Mobitz II) AV block.

3.      3rd degree (complete) AV block (with broad QRS)/ Ventricular pause > 3 sec.

4.      Bradycardia with ventricular escape complexes.

5.      Recent asystole.

6.      Denervated heart (heart transplantation).

 

Contraindications are severe hypothermia and also prolonged bradyasystoloc arrest.

 

The patient may need sedation and/or analgesia.

 

Energy setting:

1.      Set pacing rate at 80 bpm (range 60 – 90 bpm).

2.      Increase output (mA) from the minimum setting, until consistent electrical capture is achieved (wide QRS and broad T wave after each pacer’s spike). Increase 2 mA further after the previous point.

 

Note: the pacing rate width is 60 – 90bpm, however for same circumstances (e.g. complete AV block with idioventricular rhythm 50 bpm), a slower rate of 40 or even 30 bpm may be required.

 

The position of the pads on arrest is as in defibrillation. Otherwise you can choose the AP placement with the anterior electrode on the left anterior chest wall (beside the sternum, overlying the V2 & V3 ECG positions) and the posterior electrode between the lower part of the left scapula and the spine (at the same horizontal level as the anterior).

 

NOTES

·        If there is a need for TCP and the pacemaker is not immediately available, we give drugs (atropine etc).

·        In case the TCP is unsuccessful and the IV pacemaker isn’t immediately available, we give drugs such as atropine and adrenaline or dopamine infusion. 

 

 

 

 AVOIDING PITFALLS IN ALS

·        On a patient with COPD on respiratory distress do not forget to taka ABGs (arterial blood gases). In case of type II respiratory insufficiency with hypoxemia and hypercapnia, call an expert! Then max 28% oxygen is needed. That occurs because in some cases of COPD the patients rely on their hypoxic drive to breathe, so oxygen more than 30% may lead to reduced RR (respiratory rate) and hypercapnia which will cause decreased conscious level and respiratory failure with cardiac arrhythmias. So, in case on ABGs is evidence of CO2 retention, start with 24 – 28% oxygen in the above patients and reassess after 30 min. In case the patient has not evidence of CO2 retention, then start with 28 – 40% oxygen and monitor next the ABGs.

·        On operated patients check the tubes for blood and the Foley for urine.  

·        In case of suspected hypovolemia, on ABCs place also a Foley.

·        On ethical problems consult your hospital’s legal team. In case e.g. of a kid with an end stage disease (such as CF cystic fibrosis or cancer) that is intubated and the parents ask to be extubated, consider that you aren’t covered by the law. Just say that next time they should avoid bringing the kid to the hospital, or seek a court’s decision. Also comfort them that in the future there may be a therapy for the disease. There are many other legal problems such as parents – Jehovah martyrs that refuse their child to be transfused with blood, in case of trauma with hypovolaemia. 

·        In any interference we check the outcome by repeating the ABCs e.g. on a patient with shortness of breath and SpO2 oxygen saturation 89% we place a not rebreathing mask with reservoir and check then if the saturation improves. 

·        In any change (deterioration) on the patient we recheck ABCs!

·        After cardioversion we check monitor and pulse (we exclude PEA). If the arrhythmia is converted we check again ABCs.

·        We do not forget antiarrhythmic (e.g. amiodarone) maintenance infusion after a successful cardioverted or defibrillated wide complex tachycardia (we start with loading dose if already hasn’t given).

·        In case the algorithm changes, we take the Joules from the beginning and forget what we gave previously e.g. if now we have a pulseless VT, we start with e.g. 120 J (for biphasic).

·        In any change from an arrest  rhythm to another arrest rhythm (e.g. from VF to asystole) we give adrenaline following the new algorithm (e.g. immediately on asystole) irrespectively the time we gave it previously (on our previous algorithm). However, this is not the case for atropine or amiodarone (these have max dose). 

·        On a change from an arrest rhythm to a viable rhythm, we check the monitor and for pulse (to exclude PEA).

·        On a change from an arrest rhythm to another arrest rhythm we check the monitor. In case the new rhythm is VT, we check also for pulse.

·        On a change from a viable rhythm to an arrest rhythm (e.g. VT) we recheck ABCs and specifically if the patient is conscious.

 

If the patient is unconscious we call for help and check for breathing and pulse simultaneously.

 

In case the patient has no pulse we go on with the ALS algorithm. We call blue code, ask for a defibrillator and start CPR.

 

In case the patient has pulse, but does not breathe or breaths inadequately (e.g. RR respiratory rate is >30 or < 10) or if the GCS is <_8 we call blue code, ask for a defibrillator and perform BMV with self inflating bag with reservoir or we intubate (with RSI rapid sequence intubation if GCS > 3).

 

In case the patient breaths and has pulse, we place the patient on a recovery position, if unconscious. We check ABCs and specifically airway patency (airway is patent if the patient talks), respiratory rate, bilateral normal chest expansion, we perform chest auscultation and percussion, we check SpO2 oxygen saturation of hemoglobulin, we check the pulse (radial and carotid), the BP, connect to monitor, establish IV/IO access (keep it patent with normal saline  and take blood for Labs), take a 12 lead ECG and ABGs, check AVPU or GCS (with size and reaction of both pupils – also notice any abnormal posture such as stereotypical flexion or extension), expose the patient (remove clothes) and perform log roll (especially on trauma, scheck for trauma, rash, petechiae etc) and next we prevent hypothermia (blankets). We also call expert! When the patient has been stabilized, we transfer to ICU (ITU).

·        If an intubated patient improves and we have a little difficulty on ventilating or he/she bites the ET tube, we consider extubation. However, extubation should be performed rather in the ICU, rather than in the ER/ ED (emergency room/ department).  However, don’t forget that difficulty on ventilation may suggest tension pneumothorax.

·        Every drug has contraindications e.g. don’t give amiodarone on a patient with bradycardia and hypotension, but stabilize first the patient (e.g. if the patient had initially sinus bradycardia and then VF and eventually was successfully defibrillated but now has still bradycardia and hypotension we may stabilize the patient with TCP and then, when the patient is haemodynamically stabilized, we give amiodarone infusion).

·        To see if an intubated patient with a VT is unstable, we check e.g. the BP for hypotension.

·        We don’t rely only on monitor, but if available, we perform 12 lead ECG. Monitor is unreliable to show AMI (acute myocardial infarction)/ ACS (acute coronary syndrome).

·        Sodium bicarbonate is indicated in metabolic acidosis (check ABGs arterial blood gases) – e.g. on hyperkalaemia, TCAs tricyclic antidepressants, aspirin, phenobarbital, diphenydramine and cocaine) OD (overdose) and also on prolonged (>10min) arrest. Don’t give it in patients with hypercarbic acidosis.

 

Bicarbonate’s dose is 1 mEq /kg (1mMole/Kg or 1 ml/kg) of 8.4% solution IV/IO. Ventilate the patient after bicarbonate administration. Don’t give it with catecholamines (e.g. adrenaline or dopamine) at the same IV line (at least flush the line first with normal saline).

 

 

 

NEVER FORGET:

·        Safety first.

·        Push ‘sync’ synchronized button on cardioversion.

·        Remove oxygen 1 meter away or close the ventilator before the defibrillation or cardioversion.

·        Take finger stick glucose on suspected stroke (also on seizures).

·        Call blue code and ask for a defibrillator on an unconscious patient.

·        Don’t forget IV/IO access on C – circulation (take blood for labs, keep it open with normal saline).

·        Rule out and treat 6Hs & 6Ts reversible causes of arrest (especially in asystole or PEA).

·        On an unconscious patient follow the intra hospital CPR/ AED algorithm. Before checking for breathing, open the airway (chin lift or jaw thrust, jaw thrust only on trauma).

·        Do not interrupt the chest compressions (a very common mistake) for any reason. However, if needed (e.g. for intubation) interrupt it just for a few seconds. There are special devices that perform automatically chest compressions. Subclavian IV rout is also contraindicated on cardiac arrest (another common mistake) because it will interrupt the chest compressions and also may cause undetectable complications such as pneumothorax or subclavian artery puncture. Prefer femoral IV rout. If no fast access to  IV rout, go on with IO (intraosseous) rout.

 

 

 

 

APPENDIX (I): COMMON CAUSES OF SHOCK

 

 What to rule out on a shock:

a)Traumatic blood loss. Check for bleeding in chest. Perform CXR, FAST. Check for pelvic or long bone fracture. If so, do immobilization and consider PAST antishock trousers.

b)Non traumatic blood loss. Rule out abdominal aortic aneurysm (e.g. palsatile abdominal mass). Do USS/ FAST. Is there hematemesis or melena? Is fluid on Levine (NG tube) bloody? Perform endoscopy if high suspected GI bleeding.

c)Dysrhythmia. Perform an ECG.

d)Tension pneumothorax. Are there any decreased unilateral breath sounds, tracheal deviation (away from the pneumothorax), hyper-resonant hemithorax on percussion or distended neck veins (if not hypotensive with blood loss)? Don’t wait CXR. Perform needle decompression and next insert a chest tube.

e)Cardiac Tamponade.Are there distended JVD (jugular veins distension), muffled heart sounds, low ECG voltage and electrical alterance, or pulsus paradoxus? Perform FAST/ USS (ultrasound).

f)Massive pulmonary embolism. Is there hypoxemia with right ventricular strain on ECG?

g)Anaphylaxis. Is there angioedema, laryngeal edema with stridor, wheezing, hives on skin?

h)Spinal Cord Injury – Neurogenic shock with decreased HR. Check for a motor/ sensory level of paralysis and anesthesia. Take cervical spine protections. Check rectal tone and check for blood.

i)Warm skin? If so, consider sepsis, neurogenic shock, anaphylactic shock, medication overdose (e.g.β’ or Ca blockers).

j)Also rule out Poisons/ medication overdose or SEs (Side Effects)/ illicit drug abuse, Sepsis and Adrenal Insufficiency.

• PH of venous blood is usually 0,01 – 0,03 lower than the arterial blood PH. Also PCO2 is 6 mmHg higher and bicarbonate is 2 meq/L higher by using venous blood.

• Anion gap is ([Na] + [K]) – ([Cl] + [HCO3]) and normal values are 12 – 16 mEq/L (usually 10 -1 2mEq/L).  Increased anion gap occurs on DM (diabetes melitus), alcoholics, starvation, lactic acidosis, renal failure, exogenous toxins metabolized to lactate (cyanide – CN, CO, ibuprofen, strychnine, toluene, iron – Fe and INH - isoniazide), or exogenous toxins metabolized to acids (aspirin, methanol, ethanol, ethylene glucol, paraaldeyde and rarely with isopropanol), severe hypotension, seizures and hypoxemia.

• Increased osmolar gap may occur in DKA, ethylene glycole or methanol or ethanol or isopropanol poisoning. Osmolar gap ΔOsm = measured Osm – Calculated O.

 

 

APPENDIX (II): GCS

 

Eye Opening (E4)

4   0 – 1 years old: spontaneously; > 1 years old: spontaneously

3  0 – 1 years old: to shout; > 1 years old:  to verbal command (not 

 necessarily to ‘open your eyes’)

2  all ages: to pain

1  all ages: no response  

Response to pain is checked by pressing the patient’s nail’s bed with a pen. If not response, try supraorbital pressure and sterna pressure. 

 

Best Verbal Response (V5)

5  0 – 2 years old: appropriate cry, smiles;  2 – 5 years old: appropriate words and phrases; > 5 years old: oriented, converses

4  0 – 2 years old: cries; 2 – 5years old: inappropriate words; > 5 years old:  confused

3  0 – 2 years old: inappropriate cry; 2 – 5 years old: cries, screams; > 5 years old:  inappropriate words

2  0 – 2 years old: grunts; 2 – 5 years old: grunts, sounds; > 5 years old:  incomprehensible e.g. moans

1  all ages: no response

 

Best Motor Response (M6)

6  0 – 1 years old: moves spontaneously and adequately; > 1 years old:  obeys command

5  all ages: localizes pain  

4  all ages: flexion withdrawal

3  all ages: decorticate (stereotypical flexion)

2  all ages: decerebrate (stereotypical extension) 

1  all ages: no response 

 

Motor response may be e.g. ‘raise your hand’. It is the better response of any limb. Decorticate posture is characterized by flexion of upper extremities. Decerebrate posture is characterized by internal rotation of shoulder & arm pronation and limb extension.

 

 

Score: min 3, max 15. If GCS<_8 the patient needs intubation (RSI rapid sequence intubation if GCS > 3). GCS <_8 severe injury, GCS 9 –12 moderate injury, GCS 13–15 minor injury. 

 

 

APPENDIX: SIGNS OF HYPOVOLAEMIC SHOCK


Signs of hypovolaemic shock (haemorrhage - external or internal blood loss; or severe dehydration e.g. on severe diarrhea or vomiting) include: tachycardia (if not on β' blockers or pacemaker!), fast thready pulse, narrowed pulse pressure (Systolic BP - diastolic BP), weak peripheral pulses, tachypnea, decreased level of concioussness (LOC), decreased urine output (adults < 0.5 ml/kg/h, children 1ml/kg/h, infants 2 ml/kg/h), decreased capillary refill time (>2 sec), hypotension (late, with > 30% volume loss on adults and > 40% on children), cool pale skin, diaphoresis (not on dehydration); also decreased skin turgor (unreliable on the elderly) and dry mucus membranes (e.g. dry tongue) on dehydration.


NOTE

Some information in this text is empirical and its reliability can't be ascertained. It is suggested to search official medical articles, books and guidelines in order to ascertain the medical information of this text.

All the medical procedures and drug administration mentioned in this text should be done only under a senior doctor's consultancy.

 

BIBLIOGRAPHY FOR EMERGENCY & ACUTE MEDICINE


1) Stone C.K., Humphries R.L., Current Diagnosis and Treatment in Emergency Medicine, McGraw Hill - LANGE, 6th edition, 2008.


2) Wyatt J.P., Illingworth R.N., Graham C.A., Clancy M.J., Robertson C.E., Oxford Handbook of Emergency Medicine, Oxford Medical Publications, 3rd edition, 2006.


3) Ramrakha P., Moore K., Oxford Handbook of Acute Medicine, Oxford Medical Publications, 2nd edition, published 2004, reprinted 2005.


4) ALS (Advanced Life Support), European Resuscitation Council, 5th edition, The Image Factory, Belgium,2006.


5) EPLS (European Paediatric Life Support), European Resuscitation Council, 3rd edition, The Image Factory, Belgium, 2006.


6) Llewelyn H., Aun Ang H., Lewis K., Al – Abdulla A., Oxford Handbook of Clinical Diagnosis, Oxford Medical Publications, 2006.

 

7) Thomas J., Monaghan T., Oxford Handbook of Clinical Examination and Practical Skills, Oxford Medical Publications, 2008.


8) Richards D., Aronson J., Oxford Handbook of Practical Drug Therapy, Oxford Medical Publications, 2008.


9) ATLS (Advanced Trauma Life Support), American College of Surgeons – Committee on Trauma, Students Course Manual, First Impression, 7th edition, 2002.


10) PHTLS (Prehospital Trauma Life Support, basic & advanced), Prehospital Trauma Life Support Committee of the National Association of Emergency Medical Technicians in association with The Committee of Trauma of the American College of Surgeons, 5th edition (revised), Mosby, inc, 2003.


11) ALSO (Advanced Life Support in Obstetrics), American Academy of Family

Physicians, 4th edition (revised), 2006.


12) Kasper D.L., Braunwald E., Fauci A.S., Hauser S.L., Longo D.L., Jameson J.L., Harrison’s Manual of Medicine, McGraw – Hill, 16th edition, 2005.


13) Simon C., Everitt H., Kendrick T., Oxford Handbook of General Practice, Oxford Medical Publications, 2nd edition, 2005.


14) Longmore M., Wilkinson I., Turmezei T., Kay Cheung C., Oxford Handbook of Clinical Medicine, Oxford Medical Publications, 7th edition, 2008.


15) Collier J., Longmore M., Brinsden M., Oxford Handbook of Clinical Specialties, Oxford Medical Publications, 7th edition, 2006.

 

16) ACLS (Advanced Cardiac Life Support), American College of Emergency Physicians, Study Guide, 2nd edition, Jones and Bartlett Publishers, 2007.

 

  

 

 

 

 

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