ALiEMU Capsules Module 11: Acute Agitation

We are proud to present Capsules Module 11: Acute Agitation, now published on ALiEMU. We present a summary of the module with key points from a stellar module by PharmDs Jenny Koehl, Kyle DeWitt, Gabrielle Procopio, and Zlatan Coralic. When you’re finished, head over to the Capsules page for even more practical pharmacology for the EM provider.
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Reversing Anticoagulation to Administer Systemic Fibrinolytics for Ischemic Stroke: Pump the Brakes

Care of acute ischemic stroke patients is a complex and time-sensitive team effort. There is a potentially dangerous trend in the medical literature over the past few years that seems to be increasing as of late: reversing anticoagulation in order to administer systemic thrombolytic therapy. The purpose of this post is to highlight the available literature on this topic, specifically related to the direct acting oral anticoagulants (DOACs), and discuss why we should not support this practice (at least as of today).

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4 New Podcasts on the Opioid Initiative | ACEP E-QUAL Series

ACEP EQUAL opioid use podcastsThe American College of Emergency Physicians (ACEP) features 3 quality improvement targets within their Emergency Quality Network (E-QUAL) initiative: sepsis, imaging, and chest pain. Most recently, they added a fourth new focus on the opioid epidemic. This opioid initiative covers best-practice approaches and strategies for managing opioid-related complications. In collaboration with ACEP E-QUAL, we have remixed and distilled 5 of their webinars into 4 podcasts.

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By |2020-04-20T19:37:52-07:00Sep 24, 2018|Podcasts, Tox & Medications|

ACMT Toxicology Visual Pearls: Toxic Mouth Pain

betel nut mouthA middle-aged Asian female presents to the emergency department complaining of 2-3 days of mouth pain. She has chewed betel nut for a number of years. Which of the following is true regarding her presentation and management?

  1. Debridement should be avoided.
  2. Metronidazole is contraindicated due to the potential of a disulfiram-like reaction.
  3. Oral secretagogues should be used due to the anticholinergic effects.
  4. The patient is at increased risk of oral cancer.

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By |2019-11-12T19:05:57-08:00Aug 30, 2018|ACMT Visual Pearls, ENT, Tox & Medications|

Replace dolutegravir (Tivicay) with raltegravir (Isentress) for post-exposure prophylaxis

raltegravirPost-exposure prophylaxis (PEP) of patients who may have been exposed to HIV includes a combination HIV nucleoside analog reverse transcriptase inhibitor emtricitabine/tenofovir (Truvada) plus an integrase inhibitor. The CDC initially recommended the integrase inhibitor dolutegravir (Tivicay). However on May 18, 2018, the CDC placed an alert about the neural tube defect risk with dolutegravir.1 How does this change our ED practice?

The evidence

Based on an interim analysis in an ongoing safety of dolutegraivir, the U.S. Health and Human Services announced:

The concern stems from a preliminary unscheduled analysis of an ongoing NIH-funded birth surveillance study in Botswana, which has reported an increased risk of neural tube defects among infants of women who became pregnant while taking DTG [dolutegravir]-based regimens. The study reported 4 cases of neural tube defects out of 426 infants born to women who became pregnant while taking DTG-based regimens. This rate of approximately 0.9% compares to a 0.1% risk of neural tube defects among infants born to women taking non-DTG-based regimens at the time of conception.

Use raltegravir as an alternative integrase inhibitor for PEP

For men and women who are not able or likely to get pregnant, it is safe to administer dolutegravir for PEP. However for women of child-bearing age (which includes many of ED patients who are evaluated for sexual assault), these patient should instead receive raltegravir (Isentress).

Why use an integrase inhibitor with reverse transcriptase inhibitors?

Utilizing a 3-drug regimen for HIV PEP is recommended by multiple guideline committees including the CDC and WHO despite low quality evidence suggesting benefit over 2-drug regimens because of the availability of well tolerated medications. Integrase inhibitors offer a few beneficial characteristics over alternative HIV medication classes that may be included in addition to a standard nucleotide and non-nucleotide reverse transcriptase inhibitor combination (e.g. Truvada).

  1. By interfering with the integration of transcribed viral DNA into a host cell, this medication class is effective against a later state of the viral life cycle than reverse transcriptase inhibitors allowing for later efficacy following viral exposure.2
  2. Integrase inhibitors produce rapid viral suppression compared to other medication classes which may benefit individuals with recent exposure.3,4
  3. Medications in this class are generally well tolerated and have fewer drug interactions than the alternative options while offering an alternative mechanism and barrier to resistance.

PEP Dosing for HIV

  1. Emtricitabine/tenofovir (Truvada): 200 mg/300 mg (1 tablet) PO daily
  2. Raltegravir (Isentress): 400 mg PO twice daily

Because the preventative effectiveness of these medications decline over time, it is critically important to administer the first dose of each in the Emergency Department in a timely fashion. Evidence extrapolated from animal data suggests that efficacy of HIV post exposure medications decreases greatly 72 hours after exposure and should not be provided.5–7

Reference

  1. Zash R, Makhema J, Shapiro R. Neural-Tube Defects with Dolutegravir Treatment from the Time of Conception. N Engl J Med. July 2018. [PubMed]
  2. Marsden M, Krogstad P, Zack J. Virological evidence supporting the use of raltegravir in HIV post-exposure prophylaxis regimens. Antivir Ther. 2012;17(7):1375-1379. [PubMed]
  3. Hoenigl M, Chaillon A, Moore D, et al. Rapid HIV Viral Load Suppression in those Initiating Antiretroviral Therapy at First Visit after HIV Diagnosis. Sci Rep. 2016;6:32947. [PubMed]
  4. Rahangdale L, Cates J, Potter J, et al. Integrase inhibitors in late pregnancy and rapid HIV viral load reduction. Am J Obstet Gynecol. 2016;214(3):385.e1-7. [PubMed]
  5. Irvine C, Egan K, Shubber Z, Van R, Beanland R, Ford N. Efficacy of HIV Postexposure Prophylaxis: Systematic Review and Meta-analysis of Nonhuman Primate Studies. Clin Infect Dis. 2015;60 Suppl 3:S165-9. [PubMed]
  6. Martin L, Murphey-Corb M, Soike K, Davison-Fairburn B, Baskin G. Effects of initiation of 3’-azido,3’-deoxythymidine (zidovudine) treatment at different times after infection of rhesus monkeys with simian immunodeficiency virus. J Infect Dis. 1993;168(4):825-835. [PubMed]
  7. Tsai C, Emau P, Follis K, et al. Effectiveness of postinoculation (R)-9-(2-phosphonylmethoxypropyl) adenine treatment for prevention of persistent simian immunodeficiency virus SIVmne infection depends critically on timing of initiation and duration of treatment. J Virol. 1998;72(5):4265-4273. [PubMed]

The Myth of Vasopressors and Ischemia

Despite the widespread clinical use, and their well-documented life-saving properties, vasopressors are often maligned, accused of causing ischemia to fingers, toes, mesentery, kidneys, and so forth. Not only is the evidence that this happens poor, but, a fear of this dreaded complication can unwarrantedly lead good clinicians to limit or withhold potentially life- and organ-saving medications. This article showcases the importance of end-organ perfusion and explains how vasopressors may in fact be one of the most important therapies in an emergency physician’s armamentarium.
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By |2018-06-11T08:02:01-07:00Jun 11, 2018|Critical Care/ Resus, Tox & Medications|
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