Podcast # 466: Subacute Sclerosing Panencephalitis

Author: Nicholas Hatch, MD

Educational Pearls:

  • Measles has a period of infectivity starts before the appearance of the characteristic rash, up to 4-5 days
  • A devastating consequence of measles is Subacute Sclerosing Panencephalitis (SSPE), which manifests 7-10 years after the initial measles infection
  • SSPE is a central nervous system disease that has no cure and is nearly universally fatal
  • Educating patients on the importance of vaccination should include discussion of these long term consequences

References

Pallivathucal LB, Noymer A. Subacute sclerosing panencephalitis mortality, United States, 1979-2016: Vaccine-induced declines in SSPE deaths. Vaccine. 2018 Aug 23;36(35):5222-5225. doi: 10.1016/j.vaccine.2018.07.030. Epub 2018 Jul 26. PubMed PMID: 30057285.

Summarized by Will Dewispelaere, MS3 | Edited by Erik Verzemnieks, MD

Podcast # 437 : Myasthenia Gravis

 

Podcast # 437 : Myasthenia Gravis

Author: Gretchen Hinson, MD

Educational Pearls:

  • Myasthenia gravis (MG) is an antibody mediated autoimmune disorder against the acetylcholine receptors at the neuromuscular junctions.
  • Bimodal age distribution (20’s-30’s: women; 60’s-70’s: men)
  • Presents with fluctuating muscle weakness typically worse at the end of the day with upper extremities affected more than lower and typically involving facial muscles.
  • Myasthenia crisis occurs when muscle fatigue begins to cause respiratory depression
  • MG was historically diagnosed with the Tensilon test but now often by EMG
  • Treatment of MG crisis involves plasma exchange and IVIG. Those in crisis often require intubation and ICU admission

References:

Gilhus NE. Myasthenia Gravis. N Engl J Med. 2016 Dec 29;375(26):2570-2581. doi: 10.1056/NEJMra1602678. Review. PubMed PMID: 28029925.

Roper J, Fleming ME, Long B, Koyfman A. Myasthenia Gravis and Crisis: Evaluation and Management in the Emergency Department. J Emerg Med. 2017 Dec;53(6):843-853. doi: 10.1016/j.jemermed.2017.06.009. Epub 2017 Sep 12. PubMed PMID: 28916122.

Summarized by Travis Barlock, MS4 | Edited by Erik Verzemnieks, MD

Podcast # 342: Scombroid

Author: Jared Scott, MD

Educational Pearls:

  • Scombroid is a type of food poisoning associated with dark fish (i.e. tuna, salmon, mackerel) that mimics anaphylaxis.
  • Occurs through conversion of histidine to histamine by bacteria in the fish.
  • Symptoms include flushing, lips swelling, nausea, diarrhea in setting of recent fish consumption.
  • Treat with antihistamines.

 

References

Ridolo E, Martignago I, Senna G, Ricci G. Scombroid syndrome: it seems to be fish allergy but… it isn’t. Curr Opin Allergy Clin Immunol. 2016. 16(5):516-21. doi: 10.1097/ACI.0000000000000297.

Patterson R, Little B, Tolan J, Sweeney C. How to manage a urinary catheter balloon that will not deflate. Int Urol Nephrol. 2006;38(1):57-61. Review. PubMed PMID: 16502053

Podcast #330: Behcet Disease

Author: Nick Hatch, MD

Educational Pearls:

  • Behcet Disease is an autoimmune disease that can affect any organ system.
  • Typical symptoms include recurrent oral and genital ulcers, but more concerning features include skin rashes, ocular problems, and strokes.
  • Patients with Behcet disease with hypotension should have low threshold for giving steroids.

References:

Arlt W, Allolio B. Adrenal insufficiency. Lancet, 2003; 361:1881.

Sakane T, Takeno M, Suzuki N, Inaba G. Behçet’s disease. New England Journal of Medicine. 1999; 341:1284.

Podcast #276: Angioedema

Author: John Winkler, M.D.

Educational Pearls

  • Angioedema is immediately life-threatening due to airway obstruction.
  • Mechanisms include allergic reaction (histamine-related) or bradykinin-related (ACE-inhibitor, C1 esterase inhibitor deficiency).
  • The bradykinin-related mechanism will not respond to the traditional meds used for anaphylaxis. Instead, use FFP to replace depleted factors.
  • If a patient displays signs of respiratory compromise, intubation is indicated. Anesthesia should be consulted as this will be a very difficult airway.

References: https://emcrit.org/pulmcrit/treatment-of-acei-induced-angioedema/

Podcast #261: Icatibant

Author: Aaron Lessen, M.D.

Educational Pearls

  • Icatibant was introduced to treat ACE-inhibitor induced angioendema.
  • This type of angioedema is refractory to epinephrine and antihistamines, and is likely mediated by elevated bradykinin.(which is inactivated by ATII and ACE).
  • Icatibant initially was shown to reduce facial swelling and airway obstruction in the setting of ACE-I angioedema, but later, better-powered studies showed that it had no benefit compared to standard treatment.

References: Sinert R et al. Randomized Trial of Icatibant for Angiotensin-Converting Enzyme Inhibitor-Induced Upper Airway Angioedema. J Allergy Clin Immunol Pract 2017. PMID: 28552382

Podcast #226: Biphasic Anaphylaxis

Author: Sam Killian, M.D.

Educational Pearls

  • Anaphylaxis is common in the ED. These patients are treated and then usually watched for 4-6 hours.
  • Biphasic happens in patients that have a complete resolution of their anaphylaxis  for at least an hour, but then have a recurrence that requires pharmacologic  intervention. Most of the time this happens 3-6 hours later, but can happen more than 10 hours later.
  • More commonly happens in patients that have a delayed presentation,  a wide pulse pressure, need multiple doses of epi, require the use of  a beta agonist, or are ages 6-9 years old.
  • Educate patients about the possibility of Biphasic anaphylaxis before discharge. 

 

Check out this episode!

Podcast #188: Monoarthritis

Author: Peter Bakes M.D.

Educational Pearls:

  • Some common causes of monoarticular arthritis include: crystal arthropathies (gout and pseudogout), infection (septic joint), reactive arthritis and acute presentations of chronic arthritides.
  • Lyme disease usually presents with a targetoid lesion associated with constitutional symptoms
  • The common triad of symptoms associated with reactive arthritis (aka Reiter’s Syndrome) consists of conjunctivitis, urethritis, and arthritis
  • Reactive arthritis commonly presents with a history of  a GU infection (often chlamydia) or GI infection (Shigella, Campylobacter, Yersinia, Salmonella). It is more common in men and those between 20 and 40 years old.
  • Treatment for reactive arthritis is usually supportive.

References: www.emedicine.medscape.com/article/331347-overview

Podcast #171: Reiter’s Syndrome

reitersyndromRun Time:  5 minutes

Author: Peter Bakes M.D.

Educational Pearls:

  • Case presentation: 18 year old otherwise healthy male presents to the ED complaining of neck stiffness, headache, and right ankle irritation. The patient recently traveled to Italy in an area endemic of Lyme Disease. The patient 2 weeks prior had a viral infection w/ rhinorrhea and diarrhea. The patient was diagnosed the previous day with a “UTI” and is currently taking antibiotics.
  • Other important information that would be useful for evaluation would be a prior evaluation for lyme, known pre-existing joint processes, and previous rheumatoid history.
  • The patient had no rash on exam, no associate features of lyme, and no bacteria in the urine, but had noted unilateral conjunctivitis, and a red, inflamed ankle joint.
  • Possible causes of presentations of one red, warm, inflamed painful joint: Gouty arthritis, pseudogout, septic joint, lyme arthritis, acute on chronic arthritis, and reactive arthritis.
  • This patient was diagnosed with Reiter’s syndrome now known as a reactive arthritis – an antibody response to an infection. Classically presents as a genitourinary or gastrointestinal infection in a young male with the clinical triad of urethritis, conjunctivitis, and arthritis a few weeks after an infection.

Link to Podcast: http://medicalminute.madewithopinion.com/reiter-s-syndrome/

References: http://www.aafp.org/afp/2003/0701/p83.html

Podcast #81: Angioedema

q2vvyzhtetho5ulvhnarww_mRun Time: 2 minutes

Author: Dr. Nicholas Hatch

Educational Pearls:

  • Angioedema is usually caused by an allergic reaction and can be induced by ACE inhibitors as well as tissue plasminogen activator (TPA).
  • Angioedema is caused by the build up of bradykinins resulting in the leaking of capillaries and swelling of tissue.
  • TPA-induced angioedema is reported to occur in 1.6% of the patients who receive TPA and is more severe than ACE inhibitor-induced angioedema.
  • Giving solu-medrol to treat ACE inhibitor-induced angioedema is the standard of care, although its actual benefit is limited.
  • FFP and icatibant (which is a bradykinin receptor antagonist) have been shown to provide more benefit in treatment of angioedema. These are much more expensive options than solu-medrol, with the 30 mg of SubQ icatibant costing the hospital $5000 dollars per dose.
  •  ACE inhibitor-induced angioedema lasts on average 27 hours before the symptoms subside.

Link to Podcast: http://medicalminute.madewithopinion.com/angioedema/

References: http://www.uptodate.com/contents/ace-inhibitor-induced-angioedema

http://rebelem.com/tpa-associated-angioedema/

http://www.ncbi.nlm.nih.gov/pubmed/12639808