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Omnipaque 300

Radiopaque Contrast Use In Pain Medicine

Omnipaque - Iohexol (non-ionic)

By Chris Faubel, M.D. -

Radiopaque contrast agents are used by pain physicians during fluoroscopically-guided injections and other pain procedures (kyphoplasty, discography).  Their use is essential for confirming needle tip placement for eventual corticosteroid/local anesthetic administration, and to rule out inadvertent intravascular placement of the needle.

Click here for a great video of contrast being injected to confirm correct placement for a transforaminal epidural

The contrast agents are radiopaque because of the iodine content in the solution.  This iodine doesn’t allow penetration of x-rays, and therefore shows up as blackness (opaque) on the fluoroscopy monitor.  Because it is more black than other structures being x-rayed, it is easy to visualize the spread of the contrast agent.  This spread then allows the pain physician to know where the injectate (usually a corticosteroid and anesthetic) will also flow.

These radiocontrast agents can be divided into two categories: 1) Non-ionic.   2) Ionic

  • The non-ionic agents are more hydrophilic, have a lower osmolality, and therefore produce fewer adverse effects (less risk of arachnoiditis or allergic response).  Because of this, we only use non-ionic contrast agents.

The most commonly used contrast agents in pain medicine are iohexol (trade name = Omnipaque) and iopamidol (trade name = Isovue).  These two solutions have a low concentration of iodine (200-300mg/ml), which makes them safe, yet still create good imaging contrast.

Clinical pearl: You can dilute the contrast agent with sterile, normal saline (by up to 25%) and still get sufficient darkening when injected.

Allergies to Shellfish (shrimp, crawfish, lobster, crabs)

  • It has long been medical folklore that patients allergic to shellfish, would also be allergic to iodinated contrast agents because both contained iodine, and therefore there would be cross-reactivity.
  • It has since been shown that the antigenic property of shellfish is actually a particular protein, not the iodine.  [1]
Allergy Skin Testing
  • Injecting a small volume of non-ionic radiocontrast subcutaneously is NOT helpful in predicting whether that patient will have adverse reactions during a procedure.
Adverse Reactions
  • Mild reactions: urticaria (raised, itchy hives), pruritus; rhinorrhea; nausea, brief retching, and/or vomiting; diaphoresis; coughing; and dizziness.
  • Moderate reactions: more vomiting, wider spread urticaria, mild bronchospasm, facial edema, hypotension
  • Severe reactions: hypotension, severe bronchospasm, laryngeal edema, pulmonary edema, seizures, syncope, and death.
  • All of the above are much more common with ionic contrast agents, not the nonionic agents we use in pain medicine.
  • A very large case study in Japan in 1990 (337,647 cases), compared high-osmolar ionic contrasts to low-osmolar nonionic agents (like the Omnipaque and Isovue above).  They found that severe adverse drug reactions to the contrast occurred in 0.22% of the ionic and only 0.04% of the nonionic contrast media. [2]
  • In a large prospective study, the incidence of severe reactions was found to be 0%. [3].  However, in this same study, adverse effects of any severity was seen in 0.7% of patients.
  • Patients with a seafood allergy have a slightly greater risk of having an adverse reaction (of any severity) to IV contrast.  But it should be noted that this correlation was only shown with ionic contrast (which we don’t use), and that the increased risk is roughly the same as patients with allergies to eggs, milk, chocolate, strawberries, or those with asthma.  Also, 85% of patients with a seafood allergy had no adverse reaction at all to the ionic IV contrast. [7]
Gadolinium Contrast as an Alternative
  • For patients with a true history of severe allergic reaction after a prior nonionic contrast administration, gadolinium contrast (usually used as MRI contrast) can be used safely and effectively [4].
Pretreatment Options
  • Some physicians recommend just pretreating patients that are high-risk for adverse reactions, or have had adverse reactions in the past.
  • Three pretreatment regimen examples:
  1. Oral prednisone 20-50 mg, ranitidine (Zantac) 50 mg, and diphenhydramine 25-50 mg orally 12-24 hours prior to exposure by injection. An additional 25 mg of diphenhydramine can be given by IV immediately before contrast injection. [5]
  2. Methylprednisolone 32mg orally 12 hours and 2 hours before the injection. [6]
  3. Oral prednisone 50mg at 13, 7, and 1 hour before contrast injection, with Benadryl 50mg IV, IM, or PO, 1 hours before the contrast. [6]

 

References:

1) Andreas L. Lopata, and Samuel B. Lehrer.  New Insights Into Seafood Allergy.  Curr Opin Allergy Clin Immunol. 2009;9(3):270-277.

2) Katayama H, Yamaguchi K, Kozuka T, et al. Adverse reactions to ionic and nonionic contrast media. A report from the Japanese Committee on the Safety of Contrast MediaRadiology. Jun 1990;175(3):621-8.

3) Wolf GL, Arenson RL, Cross AP. A prospective trial of ionic vs nonionic contrast agents in routine clinical practice: comparison of adverse effects. AJR Am J Roentgenol. May 1989;152(5):939-44.

4) Safriel Y, Ali M, Hayt M, Ang R. Gadolinium use in spine procedures for patients with allergy to iodinated contrast–experience of 127 procedures.  AJNR Am J Neuroradiol. 2006 Jun-Jul;27(6):1194-7.

5) Anthony H Wheeler. Therapeutic Injections for Pain Management. Medscape.com. Aug 3, 2011.

6) Pradeep Chopra and Howard Smith.  Contrast Agents for the Interventional Pain Physician.  Pain Physician. Vol. 7, No. 4, 2004

7) Beaty AD, Lieberman PL, Slavin RG.  Seafood allergy and radiocontrast media: are physicians propagating a myth? Am J Med. 2008 Feb;121(2):158.e1-4.

 

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Acetaminophen

Acetaminophen in Pain Medicine

By Chris Faubel, MD –

Source: mountainside-medical.com

Names: acetaminophen / paracetamol (Tylenol)

  • Combinations with opioids
    • with tramadol = Ultracet
    • with hydrocodone = Norco, Vicodin, Lortab
    • with oxycodone = Percocet

Mechanism of Action - Analgesic

  • Weak inhibitor of prostaglandin synthesis centrally [1]
  • Has other analgesic mechanisms at the spinal cord and cerebral cortex [4]

Uses

  • Drug of choice for relieving mild to moderate musculoskeletal pain (especially osteoarthritis)
  • Acute migraine headaches:  paracetamol 1,000-mg + metoclopramide 10-mg (Reglan) is as effective as sumatriptan 100-mg [5]

Benefit over NSAIDs

  • Does NOT interfere with the anti-platelet effect of aspirin (as ibuprofen does) – no increased risk of stroke
  • Does NOT cause renal or gastrointestinal problems

Synergistic Action

Source: www.australianprescriber.com/magazine/33/4/113/5

  • The combination or concurrent use of acetaminophen with various opioid analgesics (oxycodone, tramadol, etc.) has shown synergistic effects. [3] See the image below.
  • Brings together two different but complimentary mechanisms of analgesic action.
  • Benefit: Lower individual drug doses

Metabolism

  • Microsomal enzyme system in the liver (shared by other analgesics, anticonvulsants, antibiotics, and other drugs) – including the P450
  • When taken in normal doses in healthy patients, all metabolites are eventually broken down to non-toxic end products.
  • If the patient  is a “rapid metabolizer”, takes too much, or is a chronic alcohol abuser, the metabolite “NAPQI” accumulates and is toxic to hepatocytes.
    • Glutathione in the hepatocytes normally conjugates the NAPQI to make it non-toxic.
    • Chronic alcohol abuse (3 drinks per day) induces microsomal enzymes leading to a quicker production of NAPQI (patient’s glutathione can’t keep up).
  • Excretion = urine

Overdose

  • The most common cause of acute liver failure [2]
  • Accidental overdoses are frequent because acetaminophen/paracetamol is found in many OTC products for the treatment of the flu, colds, and menstrual cramps. [for a list of products, click here]
  • Treated most commonly with intravenous N-acetylcysteine.
    • Acetylcysteine is a glutathione precursor.
  • Dosing (for older children and adults)
    • 325 to 650mg every 4-6 hours
      • Do NOT exceed
        • 4,000-mg in a 24-hour period
        • a single dose >1,000-mg
        • doses near 4,000-mg per day for > 10 days
        • a 2,000-mg daily limit in chronic alcohol abusers
    • In 2009, an FDA Advisory Panel recommended limiting the maximum daily dose to 3,000-mg, banning its combination with opioids (such as Vicodin and Percocet), and many other actions, but these are still being debated by the FDA.

REFERENCES:
1 – Graham et al.  “Mechanism of action of paracetamol”.  Am J Ther. 2005 Jan-Feb;12(1):46-55.

2 – Ostapowicz et al. “Results of a prospective study of acute liver failure at 17 tertiary care centers in the United States”  Ann Intern Med. 2002 Dec 17;137(12):947-54.

3 – Gatti et al.  ”Oxycodone/paracetamol: a low-dose synergic combination useful in different types of pain”  Clin Drug Investig. 2010;30 Suppl 2:3-14

4 – Loes, MW. (2005) “Chapter 10: Acetaminophen and Nonsteroidal Anti-Inflammatory Drugs”  Pain Medicine and Management: Just The Facts.  The McGraw-Hill Companies, Inc.

5 – Derry et al. “Paracetamol (acetaminophen) with or without an antiemetic for acute migraine headaches in adults”  Cochrane Database Syst Rev. 2010 Nov 10;11:CD008040.

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Learning to Read MRI of the Spine

These videos are produced by Dr. Donald S. Corenman, M.D., D.C. at the Vail Spine Institute.  The target audience is clearly patients, not pain specialists, but these videos are still good to use to teach residents, fellows, and inquiring patients.

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ThePainSource.com was started to provide pain medicine information on neuromusculoskeletal conditions, interventional pain procedures, journal article reviews, and other clinically-relevant information to physicians and other healthcare providers specializing in the treatment of patients with pain.