Local Anesthetic Toxicity

LOCAL ANESTHETIC TOXICITY, as available in our ED (4% cocaine and street cocaine will be addressed in a different post; tetracaine omitted). There are definitely more “caines”, but I want to address the “caines” that we use on a daily basis.

Toxic doses by drug (there are other “caines”, but these are most commonly used in our ED):

Lidocaine 1%: 4.5 mg/kg, max off-the-cuff dose is 300 mg. 1 vial is 50 mL and 500 mg, so try not to give a full vial, please.

Lidocaine 1% w/ epi: 7 mg/kg. Max dose is 500 mg or 50 mL.

Lidocaine 2% Viscous: special note that in children, as little as 5 mL can cause seizure

#paindosing Lidocaine IV dosing is 1.5 mg/kg, with a max of 200 mg, please note this is significantly below toxic dosing for local infiltration. The literature suggests 800 mg is the lower end of IV toxic dosing in adults.

Benzocaine 20% (aka hurricane spray), indicated doses are two 1 second sprays into the oropharynx (methemoglobinemia has been induced with these indicated doseages).

Bupivacaine 0.25%: 2 mg/kg, max total dose is 175 mg, or 70 mL.

Bupivacaine 0.25% w/ epi is 3 mg/kg, max total dose is 225 mg or 90 mL.

Mechanism of toxicity:

Na+ channel blockade, causing cardiac and central nervous system effects.

Methemoglobinemia is a risk for both ester and amide anesthetics, but it is more commonly associated with benzocaine and lidocaine.

Clinical effects of toxicity:

***first effects classically involve peri-oral paresthesias

Hypotension

Motor Paralysis

QRS prolongation

Tachydysrhythmia

Bradycardia -> asystole

Respiratory paralysis

Seizures

Prilocaine and Benzocaine are associated with methemoglobinemia (neither of which are used in our ED, but may be encountered OTC), so get a cooximetry.

Treatment of local anesthetic toxicity:

*Hypotension: give fluids, pressors, avoid calcium channel blockers, avoid beta blockers, avoid lidocaine.

**If systemic effects with cardiac involvement: give Intralipid 20%: This is available in room 22 (nerve block cart) and Resus 4; Dosing is 1.5 mL/kg as an IV bolus; Then make a drip of 0.25 mL/kg/min. (max 10 mL/kg/min)

***Treat seizures with Benzodiazepenes.

****If you cause methemoglobinemia, give methylene blue 1 mg/kg over 30 minutes with a repeat dose if MetHGb is >30% after 1 hour, or symptoms persist (eg, end organ damage), BUT PLEASE DRAW LABS PRIOR TO ADMINISTRATION because the dye may affect future laboratory tests that depend on photometric assay.

#intralipidspecialnote: if QRS acutely widens to greater than 120 ms, this is an indication of impending clinical decompensation and intralipid should be administered.

Final Side Note:

If a patient is allergic to any of the “caines” (cocaine included), you can always put together a 1% diphenhydramine solution, which has been shown to be non-inferior to lidocaine when infiltrated locally for anesthetic purposes. One caveat is that the time to onset of anesthesia is slightly longer.

Final, final aside: how to make 1% diphenhydramine solution

1 Get 50 mg vial of diphenhydramine, which comes in a 1 mL at our shop.

2 Get 4 mL NS in a sterile syringe, put 1 mL of 50 mg /mL and draw diphenhydramine solution into the syringe.

3 This will bring your total solution volume to 5 mL.

4 Thats 50 mg in 5 mL, or 10 mg/mL

5 Remember 1 mL weighs 1 gram, or 1000 mg.

6 Therefore 10 mg diphenhydramine to 1000 mg NS, which is a 1% solution.

7 Keep in mind some of this will eventually redistribute to the vascular compartment and eventually other tissues (eg CNS), so I would not dose more than 50 mg total for an adult-sized human.

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Ultrasound-Guided PIV Placement Part 2 POD

The following is a powerful advanced technique that can be used to troubleshoot traditional short-axis US-PIV placement.

A familiar scenario: The elusive needle tip!

  • You’re placing an US-guided PIV and going ahead with your short axis technique

  • The vessel is directly under the center of the probe, right on that Bx-guide line

  • You know exactly how deep it is

  • The needle has entered the skin… the tip should be right over or very near the vessel…

  • But where is it??? You’re bouncing the needle a little and see tissue moving, you’re slowly sweeping the probe backward and forward where your needle tip should be, but it continues to elude you! Maybe it’s a little deep, maybe there’s some echogenic (bright) tissue hiding it, doesn’t matter, here’s what to do...

The answer: Long Axis — Hear me out!

  • Take your eyes off of the ultrasound screen

  • Pick up the probe and place it back down, marker toward you, exactly along the axis of the angiocath, DIRECTLY over it!

  • Without moving your hand, look back up at the screen. Unless you’re at a crazy steep angle, you will see your whole needle clearly!

  • If you see the vessel on the screen as well, you are now perfectly set up to continue placing your IV

  • Position the tip in the vessel lumen, then advance the angiocath over the needle as you normally would

Image result for long axis ultrasound guided IV

The other scenario: You’ve positioned the probe over the needle, you look up and see the needle but not the vessel any more, or maybe part of the vessel — here’s what you do

  • Slide/rotate the probe such that you have the vessel in view at its widest diameter on the screen

  • Then LOOK BACK AT THE ARM

  • If the probe is now to the right of the needle, you need to redirect to the right; if the probe is to the left, the needle needs to go left

  • Withdraw the needle a few mm and then redirect so that it is inline with the ultrasound

  • As you do this, look back up at the screen and you should see the needle coming into view

In a nutshell: If you’ve lost your needle tip

1. Use the probe to show you where the needle is

2. Use the probe to show you where the vessel is

3. With the probe over the vessel, position the needle so that it’s directly under the probe

4. Now all three are lined up and you’re ready to position the needle tip in the vessel lumen

A few last tips:

  • You can fine-tune your left-right control of needle tip in long axis by just moving the needle slightly one way or the other and seeing if it comes more into view or less into view — this will start happening automatically if you practice this technique a few times

  • I still recommend letting go of the probe and advancing the angiocath with non-dominant hand, however if an assistant takes the probe when you are ready to advance the angiocath, you can watch it go into the vessel and ensure that it is advancing smoothly into the lumen.

  • You can do this with one person as well but this requires advancing the angiocath and stabilizing the needle with one hand, which is more difficult and gives little tactile feedback as to whether it is advancing smoothly or meeting resistance

  • Once you’re comfortable with this long-axis technique, try doing the entire procedure in long axis. This tends to work very well for deeper, straighter veins.

  • There’s no reason you can’t switch back to short once you’ve found your needle tip and repositioned it; perhaps it’s a twisty vessel with multiple turns and you need to walk it in a little more - short axis is better for navigating in the left-right direction (as long as you’ve located your needle tip!)

  • Remember the concept of "angle of insonation": the steeper your needle angle, the more difficult it will be to see your needle because fewer ultrasound beams are bouncing back to the probe (more are being deflected in a different direction)

Jonas Pologe, PGY3, Emergency Medicine, Maimonides Medical Center

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POD Aortic Dissection

A patient came to the north side today with an acute aortic dissection. Here are images obtained by the ultrasound team when the patient first came in.

A suprasternal view showing an intimal flap:

suprasternal.jpg

A short axis view of the abdominal aorta showing an intimal flap

abdominal.jpg

Diagnosis was made, BP meds started, cardiothoracic consulted, and CT expedited.

CT showed a severe type B thoracoabdominal aortic dissection:

CT-aorta.jpg

Aortic Dissection

Pathophysiology:

Tear in the intima (inner most layer), bleeding into the media (middle layer)

Pathophysiology_Theaorticdissectionsoriginatewithanintimaltearin_Ascendingaorta65Aorticarch10.jpg

Diagnosis of aortic dissection is very time sensitive:

mortality is directly proportional to time elapsed between symptom onset and diagnosis/treatment

.

How does it eventually kill you? (I think it’s important to ask this question about all disease processes)

acute aortic regurgitation —> cardiogenic shock

Cardiac tamponade —> obstructive shock

Major brach-vessel obstruction —> vasodilatory shock from dead organ or limb

Aortic rupture —> hemorrhagic shock

2 types that we care about: Stanford Type A and Stanford Type B

types.jpg

Type A

:

involves ascending aorta

— surgical — a/w aortic rupture, tamponade, aortic regurg, AMI, stroke — more common (68%)

Type B

:

does not involve ascending aorta — medical (BP control and monitoring) — a/w limb/organ ischemia  — less common, (32%) — usually originates just distal to L subclavian artery

Classic history: old person,

very hypertensive

;

abrupt onset

,

tearing/ripping chest pain

,

radiating to bac

k; a/w neuro symptoms e.g.

weakness/numbness

(due to vessel branch occlusion); a/w syncope/diaphoresis/N/V

Other risk factors include Marfan’s, connective tissue disease, FHx aortic disease, known aortic valve disease, recent aortic manipulation (e.g. TAVR, surgery), known thoracic aortic aneurysm, tobacco;  rarely 3rd trimester pregnancy, TB, syphilis,  vasculitis, blunt trauma

Classic physical: Pulse deficit (present in <20% of cases), unequal BP in upper/lower extremities, neuro deficits, signs of tamponade

Diagnosis:

Labs: basics, coags, trop, consider d-dimer (actually high sensitivity/NPV for dissection due to blood often clotting I false lumen)

CT angio aorta: gold standard for diagnosis of aortic dissection

CXR: not sensitive, not specific — sometimes mediastinal or aortic knob widening, few other nonspecific signs

TEE: is an excellent modality that’s in the works but we don’t have it operational yet

TTE: next best thing, as usual with ultrasound it’s specific but not sensitive - see below

Ultrasound for aortic dissection — obtain the following views:

Subxiphoid: look for pericardial effusion

Image result for subxiphoid effusion'

Parasternal long: look for effusion, look at the descending aorta, look for aortic regurg with color doppler and measure the aortic root (nl <4cm) if you want to be fancy

para-long.jpg

Suprasternal window:

look for dissection flap (image from University of Maryland department of cardiology)

Probe above the the patient’s sternum pointed inferoposteriorly with probe marker to patient’s left (assuming cardiology convention)

SSNV.jpg

Abdominal aorta scan: look for dissection flap from diaphragm to iliacs, also measure diameter in short and long

Management (From the AAC/AHA aortic dissection guidelines):

ACC AHA AoD Treatment-Algorithm

Note: When blood pressure is intact, first bring heart rate with beta blockers, then control pain, then see if they need further BP control.

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