The Pharm So Hard Podcast: An Emergency Medicine and Hospital Pharmacy Podcast

The Pharm So Hard Podcast: An Emergency Medicine and Hospital Pharmacy Podcast

By Jimmy Pruitt & Oscar SantaloMedicineHealth & Fitness
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The Pharm So Hard Podcast: An Emergency Medicine and Hospital Pharmacy Podcast episodes

  • Episode 18: The Management of Snake Bites with Craig Cocchio, PharmD, DABAT
    Background
    • More than 3,000 species of snakes are identified worldwide, with nearly 800 species considered venomous.
    • All venomous species are classified taxonomically into one of 4 general groups.
    • These include the families Viperidae, Elapidae, and Colubridae, as well as the Atractaspidinae, a subfamily of the Lamprophiidae family.
    • The United States is home to nearly 30 species and subspecies of venomous snakes, with many more found throughout Mexico. All belong to either the Crotalinae subfamily of Viperidae or the Elapidae family.
    • Of crotalid bites for which the type of snake is reported, about half are rattlesnake species, and the remainder copperheads and cottonmouths.
    •  Rattlesnakes are found throughout most of the United States, but encounters are most common in western and southern states.

    Rosen’s EM Textbook
    Pathophysiology of Snake Venom
    • Specific venom components are expected to be present to various degrees among all North American pit vipers.
    • Pit viper snake venom is a complex pool of more than 100 components that contribute to toxicity
    • Some examples include snake venom metalloproteinases, snake venom serine proteases, phospholipase A2, disintegrins, bradykinin potentiating peptides, C-type lectinlike peptide, and vascular endothelial growth factors.
    • The content, potency, and quantity of these components are dictated by a variety of factors that include but are not limited to the following: genus, species, age, diet, climate (season), and geography.
    • Available human and animal data suggest that venom antigens are absorbed into blood within minutes of envenomation, with peak concentrations detected within 4 hours
    Clinical Features
    Goldfrank’s Toxicologic Emergencies, 11e
    Diagnostic Testing
    • Diagnosis of North American snake envenomation is based on a history of a snakebite and presence of clinical signs of envenomation
    • Platelet counts, fibrinogen concentrations, and PTs are useful in the diagnosis of pit viper envenomation if they are abnormal.
    • However, normal results do not exclude envenomation because thrombocytopenia and coagulopathy do not develop in all patients with pit viper envenomation.
    Management
    Rosen’s EM Textbook
    Rosen’s EM
    Craig’s Article on Snake Bite Management

    https://www-ncbi-nlm-nih-gov.pallas2.tcl.sc.edu/pubmed/?term=Review+of+North+American+pit+viper+antivenoms+craig

    CroFab Website

    https://crofab.com/about-crofab/What-is-CroFab

    Anavip Website
    ANAVIP
    Craig Blog Resources
    https://empharmd.com/
    https://www.youtube.com/user/EMPharmD
    https://empharmd.com/abat-study-notes/
    Study tips for ABAT
    Related FOAM Posts

    https://empharmd.com/2019/12/07/anavip-is-the-juice-worth-the-squeeze/

    Management of Venomous Snake Bites in North America
    emDOc
    Tox and Hound – Snakes! Why’d it have to be SNAKES?
    Tox and
    Hound

    https://www.saem.org/cdem/education/online-education/m4-curriculum/group-m4-environmental/snake-bites

    Envenomations: Initial Management of Common U.S. Snakebites
    ALIEM
    https://empharmd.com/2020/02/01/abat-exam-study-guide/
    References

    Ruha A, Pizon AF. Native (US) Venomous Snakes and Lizards. In: Nelson LS, Howland M, Lewin NA, Smith SW, Goldfrank LR, Hoffman RS. eds. Goldfrank’s Toxicologic Emergencies, 11e New York, NY: McGraw-Hill; http://accesspharmacy.mhmedical.com.pallas2.tcl.sc.edu/content.aspx?bookid=2569§ionid=210277153. Accessed January 12, 2020.

    Otten EJ. Venomous Animal Injuries. In: Marx, J. A., & Rosen, P. (2014). Rosen’s emergency medicine: Concepts and clinical practice (8th ed.). Philadelphia, PA: Elsevier/Saunders. Accessed January 12, 2020.

    Cocchio C, Johnson J, Clifton S. Review of North American pit viper antivenoms. Am J Health Syst Pharm. 2020 Jan 24;77(3):175-187. 

    The post Episode 18: The Management of Snake Bites with Craig Cocchio, PharmD, DABAT appeared first on The Pharm So Hard Podcast.

    57 min
  • Episode 17: Do You Even Lift – Looking At The Metrics Used For External Benchmarking with Oscar Santalo and Joanna Longueira
    Definitions
    1. Benchmarking – Finding and implementing the best practices.  Health-system administrators are turning to benchmarking vendors for help in improving operational performance
    2. Efficiency – Avoiding waste or maximizing possible outputs from a set of resource inputs
    3. Productivity – defined as the efficient use of resources, labor, capital, land, materials, energy, information, in the production of various goods and services.
    4. Case Mix Index – is the average relative DRG weight of a hospital’s inpatient discharges, calculated by summing the Medicare Severity-Diagnosis Related Group (MS-DRG) weight for each discharge and dividing the total by the number of discharges.
    5. Diagnose Related Group – DRG- patient classification scheme which provides a means of relating the type of patients a hospital treats (specific to drugs)
    Background
    1. Goal is to find and implement the best practices of peer organizations
    2. Vendors without expertise in pharmacy practice often sell benchmarking metrics that ultimately result in the downsizing of pharmacy departments and services
    3. Goal is to find and implement the best practices of peer organizations
    4. Vendors without expertise in pharmacy practice often sell benchmarking metrics that ultimately result in the downsizing of pharmacy departments and services
    Major End Points
    1. Selecting an external benchmarking system: Select a meaningful peer comparison group, select the most meaningful key indicator metrics for comparing performance with that of peers, Understand the limitations of commercially available systems (see complete list in article)
    2. Metric examples
      1. Cost-based ratios – Total Cost per adjusted discharge, Labor cost per adjusted discharge
      1. Labor Productivity ratios – Hours worked per CMI discharge, FTEs per order processed
    3. Using DRG versus CMI in your weighted scores
    1. Pharmacy Intensity Score (PIS) Formula
    2. Σ(DRG intensity weights x DRG volumes)/ Total Admissions = Pharmacy Intensity Score
    3. PIS uses pharmaceutical resource consumption data to produce DRG-specific drug-use
      1. (0.1 to 100; DRG with highest median drug cost per admission assigned value of 100)
    Summary
    1. Strategies for selecting a vendor à meaningful peer comparison group and accuracy of financial data
    2. Vendors may use different formulas and knowing which formulas to avoid
    Reference

    Steve S. Rough, Michael McDaniel, James R. Rinehart, Effective use of workload and productivity monitoring tools in health-system pharmacy, part 1, American Journal of Health-System Pharmacy, Volume 67, Issue 4, 15 February 2010, Pages 300–311, https://doi.org/10.2146/ajhp090217.p1

    The post Episode 17: Do You Even Lift – Looking At The Metrics Used For External Benchmarking with Oscar Santalo and Joanna Longueira appeared first on The Pharm So Hard Podcast.

    10 min
  • Episode 16: How Much Do You Bench? An Overview on External Benchmarking with Oscar Santalo and Joanna Longueira
    Definitions
    1. Benchmarking – Finding and implementing the best practices.  Health-system administrators are turning to benchmark vendors for help in improving operational performance
    2. Efficiency – Avoiding waste or maximizing possible outputs from a set of resource inputs
    3. Productivity – defined as the efficient use of resources, labor, capital, land, materials, energy, information, in the production of various goods and services.
    Background
    1. Goal is to find and implement the best practices of peer organizations
    2. Vendors without expertise in pharmacy practice often sell benchmarking metrics that ultimately result in the downsizing of pharmacy departments and services
    3. Goal is to find and implement the best practices of peer organizations
    4. Vendors without expertise in pharmacy practice often sell benchmarking metrics that ultimately result in the downsizing of pharmacy departments and services
    Major End Points
    Summary
    1. External benchmarking helps seeing where your pharmacy department stands with other departments
    2. Many limitations such as:
      1. No gold standard or evidence-based literature
      2. Variability to which pharmacy departments provide distributive and clinical services
      3. Unable to incorporate outpatient services
      4. Vendors do not easily identify peer groups or reveal components of their formula
    Reference

     Steve S. Rough, Michael McDaniel, James R. Rinehart, Effective use of workload and productivity monitoring tools in health-system pharmacy, part 1, American Journal of Health-System Pharmacy, Volume 67, Issue 4, 15 February 2010, Pages 300–311, https://doi.org/10.2146/ajhp090217.p1

    The post Episode 16: How Much Do You Bench? An Overview on External Benchmarking with Oscar Santalo and Joanna Longueira appeared first on The Pharm So Hard Podcast.

    12 min
  • Episode 15: Keeping Ahead of Coronavirus. Helpful Information During the COVID-19 Pandemic With Alaina Dekerlegand, PharmD, BCIDP

    Stroll to the bottom for resources and protocols

    What is COVID-19

    COVID-19 is

    a new strain of coronavirus first identified in December 2019 in Wuhan, China

    The disease

    was initially named Coronavirus disease 2019 (COVID-19). The virus has since
    been renamed Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) which
    is why you may see different names for it.

    It is Related

    to the prior SARS-CoV which was first identified in 2003 and MERS-CoV (79% and
    50% genetic similarity)

    It is most closely

    related to 2 SARS-like coronaviruses in bats, with almost 90% genetic similarity

    Initial cases and spread linked to a seafood market in Wuhan. There are Bats and bat droppings in the market and the surrounding region, which is consistent with viral genetics.

    Mil Med Res. 2020 Mar 13;7(1):11.
    What is the Method of Transmission?

    The virus is

    spread through Human to Human transmission, via Droplets or direct contact

    Limited data

    exists thus far on surface survival time of SARS-CoV-2

    Prior coronaviruses do remain on inanimate surfaces for up to 9 days, and it’s likely that this viral strain will be very similar

    One study of

    COVID-19 infected patients, researchers Isolated the virus on many surfaces
    (fan, toilet, floor, door handle, etc.) without any cleaning of the room

    The good news is that the virus was not isolated outside of the patient’s room. Also, With proper cleaning of other rooms of COVID (+) patients, similar samples were negative in other patients

    Is it possible for asymptomatic patients to spread the infection?

    The transmission has been shown by asymptomatic carriers.

    Mean incubation period of 6.4 days in humans (95% CI 2.1 – 11.1 days).

    Early estimations from China propose almost 1/3 of infected individuals may be asymptomatic. This high estimation of asymptomatic carriers could explain the speed at which the virus has spread across the world

    What are the current statistics on the number of people affected?

    As of March 17th, the world health organization has reported over 167 thousand cases worldwide, with an overall mortality rate of 3.9% so far. They are updating their website daily with new information. The CDC has reported 4,226 cases in the US with 75 deaths, and a mortality rate of 1.8% thus far. The CDC is updating its website during weekdays, and most state departments are as well. Keep in mind that the mortality rates thus far will continue to increase, as a lot of the patients who have tested positive are still receiving care at this time. I also wanted to clear up some previous confusion thus far about the difference between CDC-reported numbers and those reported by state departments or local news stations. The CDC was previously performing confirmation tests on all (+) isolates identified by the state, which was causing a delay. They have since changed that requirement

    Is COVID-19 expected to have any seasonality?


    J Clin Virol.
    2018 Apr;101:52-56.
    Which patients are most at risk for contracting COVID-19?

    Some of the Vulnerable Populations identified thus far are elderly patients, those with a prior immunocompromising condition, or any comorbidity such as hypertension. Some studies have shown up to 50% of patients with at least one chronic condition. This doesn’t mean that other populations are not at risk. These are the patient populations that have been diagnosed in the highest frequency thus far, but it is likely that other patients with non-severe symptoms are not presenting for testing.

    What are the symptoms associated with COVID-19 infection?

    Most symptoms are consistent with those of other respiratory viral illnesses. The most commonly reported symptom thus far is fever (83- 96% of patients depending on the pt cohort), followed by cough (68-82%). Other symptoms include shortness of breath, rhinorrhea, muscle aches, and confusion. Gastrointestinal symptoms are relatively uncommon, but were reported in 1-3% of patients.

    What other laboratory tests and Diagnostics are used to diagnose COVID-19?

    Official COVID-19 tests are being provided by the CDC to state laboratories. Every hospital should have in place or be developing a process for screening patients and obtaining tests from their state labs if patients qualify for testing.

    What are Possible Treatment Options?

    I want to stress up front that everything we have is experimental at this point. The mainstay of therapy for treating COVID-19 patients is still supportive care, but there are some agents with possible benefits based upon in vitro activity as well as very limited clinical data.

    Guo YR, Cao QD, Hong ZS, et al. The origin, transmission and clinical therapies on coronavirus disease 2019 (COVID-19) outbreak – an update on the status. Mil Med Res. 2020;7(1):11
    Supportive Care for COVID Patients
    Are there any drugs to avoid in a COVID+ patient?

    There is a lot of information that we

    just don’t know yet. However, there are a few things being discussed so far.

    Corticosteroids: Prior studies have shown negative outcomes with corticosteroid use in respiratory viral infections. One study with the middle eastern coronavirus showed that corticosteroid therapy was associated with a significant delay in viral RNA clearance. We don’t have data yet for the effect of corticosteroids on this SARS-coronavirus 2 strain. Most experts are currently recommending AGAINST the use of corticosteroids in patients with COVID-19 infections. This is more tricky in patients with underlying COPD or those that develop ARDS. Use clinical judgment in those cases.

    ACEi/ARBs: there are currently discussions going on surrounding ACE inhibitors and ARBs. In vitro, SARS-CoV-2 is thought to use ACE2 as a binding site. Patients on ACE inhibitors have increased the production of ACE2 on cells as a result of their ACE inhibitor therapy. The current recommendation is to discontinue ACE inhibitors or ARBs in patients diagnosed with COVID-19 infections since there is a possibility that therapy may increase the rate of infection of host cells by viral particles. This is probably easy to do, as these patients will often develop sepsis and hypotension at some point during their infection course.

    NSAIDs: French authorities recently advised against the use of NSAIDs, as they may worsen the clinical course of coronavirus. Although there is no specific data yet, this is likely due to an immunosuppressive effect similar to corticosteroids, as well as an upregulation of ACE2 similarly to ACE inhibitors. At this point, it would be a good idea to avoid NSAIDs in these patients and use acetaminophen instead.

    How should we handle situations like cardiac arrests for patients who are either suspected or confirmed COVID-19?

    The answer to this question will differ based upon the design of each hospital and your standard workflow for code response. All healthcare personnel actively resuscitating the patient should be wearing appropriate N95 masks, especially if the patient is not intubated. Respiratory should be hopefully intubating them as quickly as possible if they weren’t intubated prior to the code. The number of personnel inside patient rooms should be limited in order to decrease exposure and also conserve our limited supply of PPE. One option is to have the medicine components of the code cart outside if the room for preparation, and then carefully pass compounded medications to personnel in the room. Be sure to discuss this process workflow at your institution.

    What can we do to help decrease transmission?

    We should

    follow all of the recommendations provided by the CDC thus far:

    Avoid

    handshaking, Clean hands often, Avoid touching your face, Cover coughs and
    sneezes, Disinfect surfaces regularly especially if they are shared, Handle
    food carefully. Limit travel to necessary reasons

    And try to

    avoid spending time in crowded restaurants and bars. I know that a lot of us
    are young and healthy and relatively unconcerned about COVID-19 because we
    would not have a high mortality risk if we contracted the virus. However, most
    of us are taking care of very high-risk patients and we don’t want to be the
    cause of anyone becoming sick.

    There will be a lot of meetings in the coming months with updates on patient care: Videoconference when possible for meetings. (limit in-person meetings to those with <10-15 people if possible). Make sure any in-person meetings are held in open, well-ventilated spaces

    If you or a family member is feeling sick, STAY HOME. Although our immune systems may limit the illness to mild symptoms, we may be carriers and spread the virus to our patients with weakened immune systems. In areas being hit hard thus far, there are reports of 10% of the workforce being out due to illness. We will already be stretched thin, and spreading the virus amongst each other could be catastrophic.

    What can we do about the limited supplies worldwide?

    The level of public panic has led to some crazy behaviors. Everything from toilet paper hoarding to buying up massive amounts of medical supplies, such as masks and cleaning supplies. Patients who use alcohol swabs on a daily basis for self-injection of medications are having difficulty finding them, and hospitals are having trouble obtaining masks. We can do our best to encourage everyone to be mindful of the needs of others and only buy what you and your family would reasonably need as a 1 month supply, which is the current recommendation. Try to keep members of our community informed that masks alone will not prevent spread– Encourage hand hygiene and social distancing instead. In the hospital, use of masks should be limited to essential personnel so we can conserve what we have

    Related Posts and References
    • CDC
      • https://rebelem.com/wp-content/uploads/2020/03/COVID-19-Fact-Sheet.pdf
      • https://rebelem.com/wp-content/uploads/2020/03/Suspected-COVID-19-Fact-Sheet.pdf
    • Johns Hopkins Tracker
      • https://www.arcgis.com/apps/opsdashboard/index.html#/bda7594740fd40299423467b48e9ecf6
    • Pulmcrit
      • https://emcrit.org/ibcc/covid19/
      • https://emcrit.org/pulmcrit/split-ventilators/
    • REBELEM
      • https://rebelem.com/covid-19-the-novel-coronavirus-2019/
    • UW Medicine COVID-19 Resource Site
      • https://covid-19.uwmedicine.org/Pages/default.aspx
      • https://em.uw.edu/faculty/uw-department-emergency-medicine-edicu-covid-19-preparedness
    • EMPharmD.com
      • https://empharmd.com/2020/03/15/hydroxychloroquine-for-sars-cov-2/
    • Global MediXchange for Combating COVID-19
      • https://covid-19.alibabacloud.com/
    • WHO
      • https://www.who.int/emergencies/diseases/novel-coronavirus-2019
    • King’s Critical Care
      • https://www.dropbox.com/s/6glielky1ux4w5f/King%27s%20Critical%20Care%20COVID%20Summary.pdf?dl=0
    • Critical Care North Hampton
      • https://criticalcarenorthampton.com/2020/03/08/covid-19-your-one-stop-resource/
    References
    1. Zu F, Yu T, Du R, at al. Clinical course and risk factors for mortality of adult inpatients with COVID-19 in Wuhan, China: a retrospective cohort study. Lancet 2020.
    2. Grasselli G, Pesenti A, Cecconi M. Critical Care Utilization for the COVID-19 Outbreak in Lombardy, Italy: Early Experience and Forecast During an Emergency Response. JAMA 2020.
    3. KCDC. Updates on COVID-19 in Korea. March 14, 2020. https://www.cdc.go.kr/board/board.es?mid=a30402000000&bid=0030 (Accessed on March 14, 2020).
    4. Cai J, Xu J, Lin D, et al. A Case Series of children with 2019 novel coronavirus infection: clinical and epidemiological features. Clin Infect Dis 2020.
    5. Liu W, Zhang Q, Chen J, et al. Detection of Covid-19 in Children in Early January 2020 in Wuhan, China. N Engl J Med 2020.
    6. Liu YC, Liao CH, Chang CF, et al. A Locally Transmitted Case of SARS-CoV-2 Infection in Taiwan. N Engl J Med 2020.
    7. Wei M, Yuan J, Liu Y, et al. Novel Coronavirus Infection in Hospitalized Infants Under 1 Year of Age in China. JAMA 2020.
    8. Zhu N, Zhang D, Wang W, et al. A Novel Coronavirus from Patients with Pneumonia in China, 2019. N Engl J Med 2020; 382:727.
    9. Lu R, Zhao X, Li J, et al. Genomic characterisation and epidemiology of 2019 novel coronavirus: implications for virus origins and receptor binding. Lancet 2020; 395:565.
    10. Perlman S. Another Decade, Another Coronavirus. N Engl J Med 2020; 382:760.
    11. Tang X, Wu C, Li X, et al. On the origin and continuing evolution of SARS-CoV-2. National Science Review 2020.
    12. Li Q, Guan X, Wu P, et al. Early Transmission Dynamics in Wuhan, China, of Novel Coronavirus-Infected Pneumonia. N Engl J Med 2020.
    13. Li Z, Yi Y, Luo X, et al. Development and Clinical Application of A Rapid IgM-IgG Combined Antibody Test for SARS-CoV-2 Infection Diagnosis. J Med Virol 2020.
    14. Centers for Disease Control and Prevention. Interim Clinical Guidance for Management of Patients with Confirmed 2019 Novel Coronavirus (2019-nCoV) Infection, Updated February 12, 2020. https://www.cdc.gov/coronavirus/2019-ncov/hcp/clinical-guidance-management-patients.html (Accessed on February 14, 2020).
    15. Tang A, Tong ZD, Wang HL, et al. Detection of Novel Coronavirus by RT-PCR in Stool Specimen from Asymptomatic Child, China. Emerg Infect Dis 2020; 26.
    16. Wang W, Xu Y, Gao R, et al. Detection of SARS-CoV-2 in Different Types of Clinical Specimens. JAMA 2020.
    17. Zhou P, Yang XL, Wang XG, et al. A pneumonia outbreak associated with a new coronavirus of probable bat origin. Nature 2020.
    18. Yu P, Zhu J, Zhang Z, et al. A familial cluster of infection associated with the 2019 novel coronavirus indicating potential person-to-person transmission during the incubation period. J Infect Dis 2020.
    19. Bai Y, Yao L, Wei T, et al. Presumed Asymptomatic Carrier Transmission of COVID-19. JAMA 2020.
    20. Hu Z, Song C, Xu C, et al. Clinical characteristics of 24 asymptomatic infections with COVID-19 screened among close contacts in Nanjing, China. Sci China Life Sci 2020.
    21. orld Health Organization. Director-General’s remarks at the media briefing on 2019-nCoV on 11 February 2020. https://www.who.int/dg/speeches/detail/who-director-general-s-remarks-at-the-media-briefing-on-2019-ncov-on-11-february-2020 (Accessed on March 12, 2020).
    22. Centers for Disease Control and Prevention. 2019 Novel coronavirus, Wuhan, China. Information for Healthcare Professionals. https://www.cdc.gov/coronavirus/2019-nCoV/hcp/index.html (Accessed on March 12, 2020).
    23. World Health Organization. Novel Coronavirus (2019-nCoV) technical guidance. https://www.who.int/emergencies/diseases/novel-coronavirus-2019/technical-guidance (Accessed on March 12, 2020).
    24. WHO Director-General’s opening remarks at the media briefing on COVID-19 – 24 February 2020 https://www.who.int/dg/speeches/detail/who-director-general-s-opening-remarks-at-the-media-briefing-on-covid-19—24-february-2020 (Accessed on March 15, 2020).
    25. National Health Commission of the People’s Republic of China. New coronavirus cases rise to 571 in Chinese mainland. March 15, 2020. http://en.nhc.gov.cn/2020-01/23/c_76004.htm (Accessed on March 15, 2020).
    26. Guo YR, Cao QD, Hong ZS, et al. The origin, transmission and clinical therapies on coronavirus disease 2019 (COVID-19) outbreak – an update on the status. Mil Med Res. 2020;7(1):11. Published 2020 Mar 13. doi:10.1186/s40779-020-00240-0
    27. Arabi YM, Asiri AY, Assiri AM, Aziz Jokhdar HA, Alothman A, Balkhy HH, et al. Treatment of Middle East respiratory syndrome with a combination of lopinavir/ritonavir and interferon-β1b (MIRACLE trial): statistical analysis plan for a recursive two-stage group sequential randomized controlled trial. Trials. 2020;21(1):8.
    28. Chu CM, Cheng VC, Hung IF, Wong MM, Chan KH, Chan KS, et al. Role of lopinavir/ritonavir in the treatment of SARS: initial virological and clinical findings. Thorax. 2004;59(3):252–6.
    29. Cvetkovic RS, Goa KL. Lopinavir/ritonavir: a review of its use in the management of HIV infection. Drugs. 2003;63(8):769–802.

    The post Episode 15: Keeping Ahead of Coronavirus. Helpful Information During the COVID-19 Pandemic With Alaina Dekerlegand, PharmD, BCIDP appeared first on The Pharm So Hard Podcast.

    36 min
  • Episode 14: High-Dose Nitroglycerin for Sympathetic Crashing Pulmonary Edema (SCAPE) with Rachel Wein, PharmD, BCPS
    Download Pharmacy Friday Pearl Handout
    High-Dose-Nitroglycerin-for-SCAPE-Handout.-pharmacy-friday-Pearls-2.0-Download
    Introduction
    1. Acute heart failure (AHF) is a common underlying cause for dyspnea in patients presenting to EDs around the globe.1-2  SCAPE is a subset of hypertensive heart failure which develops rapidly due to an abrupt increase in catecholamine release, subsequently leading to increased pulmonary capillary permeability and flooding of alveolar space.3-5  Patients with SCAPE present with an abrupt onset of shortness of breath which progresses over minutes-to-hours into life-threatening pulmonary edema. This is unlike other subsets of AHF, which  traditionally progress over days.3-5 Patients often present with extremely severe respiratory distress, restlessness, diaphoresis, and hypoxia on arrival to the ED. Patients may also be tachycardic with marked hypertension, suggesting elevated sympathetic activity in vivo.3-7 Nitroglycerin reduces preload and, at higher doses (> 50 mcg/min), also reduces afterload. Thus, it is imperative to initiate nitroglycerin at high, effective doses in a timely manner to treat the underlying pathophysiology.4 Multiple studies have validated the use of high dose nitroglycerin with improvement in patient-centered outcomes which include reduction in patients requiring intubation, intensive care unit (ICU) admission, hospital length of stay, and decreased myocardial infarction.8-13
    Pathophysiology
    Agrawal et al “Underlying pathophysiologic mechanisms are similar for AHFS and SCAPE. However, there are notable differences between the two.SCAPE develops over minutes-to-hours into a life-threatening condition.” “Sympathetic system is an important factor in cardiovascular physiology. Left ventricular dysfunction predisposes to an abrupt increase in sympathetic tone and release of catecholamines that can precipitate flash pulmonary edema.   Increased catecholamines cause increased heart rate and decreased diastolic time. It causes activation of the renin-angiotensin-aldosterone system (RAAS), which further worsens diastolic stiffening and increased diastolic pressures causing pulmonary fluid overload.   Increased sympathetic tone adversely affects the pulmonary circulation by increasing permeability and/or provoking stress failure of the pulmonary capillaries. Other factors contributing to flash pulmonary edema include decreased nitric oxide and increased endothelin activity.”
    Pharmacology
    Pharmacology
    Mechanism of Action Nitroglycerin, an organic nitrate, is a vasodilating agent that relieves tension on vascular smooth muscle and dilates peripheral veins and arteries.  Increases guanosine 3’5′ monophosphate (cyclic GMP) in smooth muscle and other tissues by stimulating guanylate cyclase through the formation of free radical nitric oxide. This activity results in dephosphorylation of the light chain of myosin, which improves the contractile state in smooth muscle results in vasodilation
    Dose
    Chest pain: 5-400 mcg/min (starting at 5)Pulmonary edema/afterload: 50-400mcg/min Titrate to symptom
    improvement and tolerated blood pressure
    Administration
    IV infusion: 50-400 mcg/min until symptom resolution

    IV bolus: 400-2000 mcg in syringe over 2-5 min

    Sublingual: 2-4 tablets (equivalent to 160-320 of IV nitroglycerin)

    Ointment: slow onset 30-60 min
    PK/PD
    Onset: IV 1-5 min; Sublingual 1-3 min
    Peak: IV/sublingual 3-15 min                          
    Duration: IV 5-10 min, sublingual 10-60 min
    Elimination: 22% renal
    Adverse Effects
     
     
     
     
    Headache, Hypotension, Syncope, Rebound hypertension, Tolerance with prolonged use  ~24 hours
    Drug Interactions and
    warnings
    PDE inhibitors, Aortic stenosis, preload dependent cardiomyopathy, hypertrophic obstructive cardiomyopathy, hypotension at any time
    Compatibility
    Incompatible with levofloxacin, Bactrim, daptomycin, and phenytoin
    Pearls for Nitroglycerin for SCAPE
    Pearls for Nitroglycerin for SCAPE
    Indications to Initiate
    SCAPE with SBP ≥ 160 mmHg or MAP ≥ 110 mmHg
    Inclusion
    criteria
    Adults ≥ 18 years old  
    Respiratory distress on NIV defined by ONE of the following (a–d):
    a. Tachypnea (RR > 30 breaths/min)
    b. Significant dyspnea (use of accessory muscles or air hunger)
    c. Significant hypoxia (SpO2 ≤ 90% on room air or ≤ 95% on supplemental oxygen)
    d. Presentation with pulmonary rales or B-lines over superior anterior lung fields on POCUS  

    Consecutive readings of SBP ≥ 160 mmHg or MAP ≥ 120 mmHg
    Contraindications
    Without a diagnosis of AHF and pulmonary edema

    SBP < 160 mmHg

    Significant drug interaction with nitroglycerin (i.e., PDE3 inhibitors, riociguat)

    Preload dependent patients (inferior myocardial infarction)
    Monitoring
    and Documentation
    Every 5 minutes or until symptom resolution as determined by the provider.

    Blood pressure, heart rate, RR, SpO2, symptoms of respiratory distress
    Criteria for Symptomatic Resolution (must meet two of the following)
     
    Criteria for Symptomatic Resolution
    (must meet two of the following)
    Resolution of tachypnea defined by RR decrease by 25% of initial reading OR RR ≤ 24 breaths/min

    Resolution of dyspnea defined by the use of accessory muscles or air hunger

    Resolution of hypoxia defined by SpO2 ≥ 90% on room air or ≥ 95% on supplemental oxygen

    SBP < 140 mmHg or MAP reduced by >40%
     
    Overview of Evidence
    Author, year
    Design/
    sample size
    Intervention
    & Comparison
    Outcome
    Hsieh,
    2018
    Case report
     
    n=3
    Nitrostat 0.6 mg/tab x 3
     
    IV NTG bolus 1 mg every 2 min*
     
    IV NTG infusion 40 mcg/min*
     
    *If prior therapy failed
     
    High dose NTG associated with
    Normalize respiratory
    status,No intubation + no
    ICU admission
    Paone,
    2018
    Case report
     
    n= 1
    IV NTG infusion  
    400 μg/min
    titrated by 50 mcg/min
    High
    doses bolus associated with:
    Symptomatic resolution
    @ 6 minutes*
    Wilson,
    2016
    Observational cohort
     
    N=395
    IV NTG bolus 500–2000 mcg Q3–5 min
                   vs
     
    IV infusion 20–35 mcg/min
     
                   vs
     
    IV
    bolus+ infusion
    High
    doses bolus associated with:
    Decreased ICU admission Shorter LOS No differences in adverse outcomes (intubation)
     
    Levy,
    2007
    Observational, single arm study
     
    n=29
    IV NTG
    Bolus 2 mg IV every 3 min
    High dose bolus associated with:
    Reduced intubation, need for bilevel positive
    pressure ventilation, and ICU admission
    Sharon, 2000
    RCT
     
    n=
    40
    IV bolus isosorbide 4 mg Q4 min
     
                         vs
     
    Isosorbide
    infusion starting @ 10 mcg/min + BiPAP
    High dose bolus associated with:
    Decrease intubations,
    MI, mortality, and Improved Pao2
    Cotter, 1998
    RCTn= 104
    IV isosorbide dinitrate 3 mg q5 min +
    furosemide  50 mg
     
                      vs
     
    IV isosorbide infusion 16 mcg/min titrate q15min +
    furosemide 80 mg q15 min
     
    High dose bolus associated with:
    Reduction in mechanical ventilation, MIImprovement in Pa02 and RR,Less adverse effects
     
    Related FOAM Posts
    https://emcrit.org/emcrit/scape/

    https://www.grepmed.com/images/3068/sympathetic-management-treatment-pulmonary-crashing-scape-edema

    Acute Pulmonary Edema
    Myths in Heart Failure: Part II – ED Management

    https://www.emnote.org/emnotes/high-dose-ntg-boluses

    https://wikem.org/wiki/Sympathetic_crashing_acute_pulmonary_edema_(SCAPE)

    References
    1. Nitroglycerin. Micromedex [Electronic version].Greenwood Village, CO: Truven Health Analytics. Retrieved February 5, 2020, from http://www.micromedexsolutions.com/
    2. Fromm RE, Jr, Varon J, Gibbs LR. Congestive heart failure and pulmonary edema for the emergency physician. J Emerg Med. 1995;13:71–87
    3. Howlett JG. Current treatment options for early management in acute decompensated heart failure. Can J Cardiol. 2008;24(Suppl B):9B–14B.
    4. Kramer K, Kirkman P, Kitzman D, Little WC. Flash pulmonary edema: Association with hypertension and reoccurrence despite coronary revascularization. Am Heart J. 2000;140:451–5.
    5. Gandhi SK, Powers JC, Nomeir AM, Fowle K, Kitzman DW, Rankin KM, et al. The pathogenesis of acute pulmonary edema associated with hypertension. N Engl J Med. 2001;344:17–22
    6. Agrawal N, Kumar A, Aggarwal P, Jamshed N. Sympathetic crashing acute pulmonary edema. Crit Care Med. 2016;20:39–43.
    7. Mebazaa A, Yilmaz MB, Levy P, Ponikowski P, Peacock WF, Laribi S, et al. Recommendations on pre-hospital & early hospital management of acute heart failure: a consensus paper from the Heart Failure Association of the European Society of Cardiology, the European Society of Emergency Medicine and the Society of Academic Emergency Medicine. Eur J Heart Fail. 2015;17:544–58.
    8. Viau DM, Sala-Mercado JA, Spranger MD, O’Leary DS, Levy PD. The pathophysiology of hypertensive acute heart failure. Heart. 2015;101:1861–7.
    9. McMurray JJ, Adamopoulos S, Anker `, Auricchio A, Bohm M, Dickstein K, et al. ESC guidelines for the diagnosis and treatment of acute and chronic heart failure 2012: the task force for the diagnosis and treatment of acute and chronic heart failure 2012 of the European Society of Cardiology. Developed in collaboration with the Heart Failure Association (HFA) of the ESC. Eur J Heart Fail.2012;14:803–69.
    10. Yancy CW, Jessup M, Bozkurt B, Butler J, Casey DE, DraznerMH, et al. 2013 ACCF/AHA guideline for the management of heart failure: a report of the American College of Cardiology Foundation/American Heart Association task force on practice guidelines. J Am Coll Cardiol. 2013;62:e147–239.
    11. Hsieh Y et al. Treating acute hypertensive cardiogenic pulmonary edema with high-dose nitroglycerin. Turk J Emerg Med. 2018; 18(1): 34–36.
    12. Wilson SS et al. Use of nitroglycerin by bolus prevents intensive care unit admission in patients with acute hypertensive heart failure. Am J Emerg Med. 2017;35(1):126–31.
    13. Levy P et al. Treatment of severe decompensated heart failure with high-dose intravenous nitroglycerin: a feasibility and outcome analysis. Ann Emerg Med. 2007;50:144–52.
    14. Sharon A et al. High-dose intravenous isosorbide-dinitrate is safer and better than Bi-PAP ventilation combined with conventional treatment for severe pulmonary edema. J Am Coll Cardiol. 2000;36(3):832-7.
    15. Cotter G et al. Randomised trial of high-dose isosorbide dinitrate plus low-dose furosemide versus high-dose furosemide plus low-dose isosorbide dinitrate in severe pulmonary oedema. Lancet. 1998;351(9100):389-93.
    16. Paone S, Clarkson L, Sin B, et al. Recognition of Sympathetic Crashing Acute Pulmonary Edema (SCAPE) and use of high-dose nitroglycerin infusion. Am J Emerg Med. 2018;36(8):1526.e5-1526.e7.
    17. López-Rivera F, Cintrón Martínez HR, Castillo LaTorre C, et al. Treatment of Hypertensive Cardiogenic Edema with Intravenous High-Dose Nitroglycerin in a Patient Presenting with Signs of Respiratory Failure: A Case Report and Review of the Literature. Am J Case Rep. 2019 Jan 21;20:83-90.
    18. Clemency BM, Thompson JJ, Tundo GN. Prehospital high-dose sublingual nitroglycerin rarely causes hypotension. Prehosp Disaster Med. 2013 Oct;28(5):477-81.

    The post Episode 14: High-Dose Nitroglycerin for Sympathetic Crashing Pulmonary Edema (SCAPE) with Rachel Wein, PharmD, BCPS appeared first on The Pharm So Hard Podcast.

    28 min
  • Episode 13: Assessing Pharmacy Candidates for Pharmacy Residency Programs with Dan Hu
    Questions for Dan Hu
    • Can you descript how you got interested in evaluating pharmacy students for residency?
    • What are some of the current challenges of evaluating students in the current model?
    • Can you summarize your publication “ A Screening Tool to Identify Qualified Pharmacy Residency Candidates”
    • What are some strategies that schools and university of pharmacy could incorporate into their curriculum to make students more competitive for residency programs?
    • What are your tips for students applying for PGY1 and PGY1 residents applying to PGY2 to make themselves more competitive for the PhorCAS application process?
    • What something you wish you would have known prior to applying to residency?
    • What’s your thoughts on the future of pharmacy residency/fellowship training?
    • Sample Residency Scorecard

       

      Must Read Articles about Pharmacy Candidate Residency Selection

      PMID:31223154  

      PMID: 27698497

      PMID: 27402987

      PMID: 24106162

      References
      • Hu D, Veenhouwer D, McCoy J, Caselnova DA 3rd. A Screening Tool to Identify Qualified Pharmacy Residency Candidates. Am J Pharm Educ. 2019;83(4):6714. doi:10.5688/ajpe6714
      • Hu D. Predicting Success in Residency: The Quarterback Problem. Hosp Pharm. 2016;51(8):615–617. doi:10.1310/hpj5108-615
      • Phillips JA, McLaughlin MM, Rose C, Gallagher JC, Gettig JP, Rhodes NJ. Student Characteristics Associated with Successful Matching to a PGY1 Residency Program. Am J Pharm Educ. 2016;80(5):84. doi:10.5688/ajpe80584
      • Gohlke AL, Ray DB, El-Ibiary SY, Barletta JF. Characteristics of the ideal postgraduate year 1 pharmacy practice residency candidate: a survey of residency program directors. J Pharm Pract. 2014;27(1):84–88. doi:10.1177/0897190013504962
      • The post Episode 13: Assessing Pharmacy Candidates for Pharmacy Residency Programs with Dan Hu appeared first on The Pharm So Hard Podcast.

        39 min
      • Episode 12. Mergers and Acquisitions with Oscar Santalo PharmD, MBA, MHA, BCPS
        Definition
        • Merger & Acquisition – defined as the consolidation of companies.
          • Differentiating the two terms, Mergers is the combination of two companies to form one, while Acquisitions is one company taken over by the other
        Background
        • Throughout the 1990s, mergers and acquisitions were prominent in the healthcare sector. After a drastic decline in the early 2000s, there was a resurgence of mergers and acquisitions in the market in the last ten years. According to Kaufman Hall, after just 50 health-system mergers and acquisition consolidations in 2009, the number has increased to 115 consolidations in 2017.
        • One major contrast between mergers and acquisitions is the propensity for acquisitions to become hostile
        • Vertical mergers occur when complement products or services consolidate. As it relates to healthcare, examples of vertical mergers include an outpatient pharmacy merging with a generic medication manufacturer, or CVS Health’s plan to purchase Aetna (2). Vertical mergers do not remove a competing substitute from the market, and for that reason carry less risk of violating federal antitrust laws.
        • Financial implications: Cost savings remains a driver in the pursuit of hospital consolidation

        Horizontal mergers inherently lessen competition by removing an alternative source of a particular product or service from the consumer market. However, horizontal mergers may also create more efficient companies through reduced redundancies in services, lower capital expenses through shared resources, and supply chain savings obtained through large volume purchasing.

        Operational Services

        Strategic plan where vision should focus on pharmaceutical care and highlight the strengths of each department that add value to the organization

        • Opportunities in budgeting a volume-based discounts on drug purchasing utilizing group purchasing organizations (GPO), formulary management and standardization, perpetual inventories, and direct manufacturer contracts, cost savings can be realized.
        • Concerns: Staffing productivity, formulary mgmt.
        Clinical Services
        • Pharmacy departments within expanding health-systems may undergo a drastic overhaul to the clinical services provided by their department following consolidation.
        • Hospitals entering a larger health-system may be faced with required implementation of established pharmacy services including the use of therapeutic interchanges, intravenous to oral conversions, dose rounding, and therapeutic drug monitoring protocols used throughout the existing system. These services can be accomplished through the utilization of clinical decision support systems (CDS).
        • Pharmacy departments and health-systems will need to create and manage their inpatient formulary
        Summary
        1. M&As impact pharmacies financially through labor, supply chain, and strategy
        2. Opportunities in buying power and organizational support when merging with a larger system
        3. Formulary mgmt., clinical services, and productivity should be the highest of concerns
        • Twitter
        • Linkedin
        References

        Iredell B, Farano J, Corsi MP, Santalo O, Covert A. Clinical and financial impacts on pharmacy surrounding health-system mergers and acquisitions [published online ahead of print, 2019 Dec 1]. Am J Health Syst Pharm. 2019;zxz263. doi:10.1093/ajhp/zxz263. [PMID: 31788688]

        The post Episode 12. Mergers and Acquisitions with Oscar Santalo PharmD, MBA, MHA, BCPS appeared first on The Pharm So Hard Podcast.

        15 min
      • Episode 11: The Role of an ED Pharmacist as Part of the Trauma Team with Ruben Santiago, Pharm.D., BCPS, BCCCP
        The Trauma team members

        There are many key members of the trauma team that include the trauma nurses, respiratory technicians, ED physicians, trauma surgeons, medical residents, PA/NPs, radiology techs, and anesthesiologists.

        What is a trauma center and what makes them unique?
        • Trauma centers are centers that are equipped to treat the most critical of patients who suffer from traumatic injury.
        • This includes blunt trauma such as falls and motor vehicle crashes as well as penetrating trauma (like our gun and knife club members).
        • Trauma centers are usually designated by levels (level one, level two, and so on) and are defined based on the resources available and the number of patients treated annually.
        What advice would you give ED pharmacists regarding training/certification that would help in trauma resuscitation?

        Hands-on training is your best friend for these patients.

        Being able to anticipate the team’s needs for trauma patients is key.

        • You have to know where your medications are stored, what medications are immediately available and which medications you need to expedite from your central pharmacy.
        • You also have to know where your supplies are stored such as your needles, IV pumps, IV tubing, etc.
        • Know your code cart and where it is located, so you are ready for any patients that either present in traumatic arrest or decompensate into cardiac arrest.
        What is the Primary Survey?

        The primary survey is a systematic way of evaluating a trauma patient. It consists of A for airway, B for breathing, C for circulation, D for disability, and E for exposure.

        What parts are pharmacists involved in?

        I believe the trauma pharmacist is a part of every single step in the primary survey:

        A
        • Airway:
          • A pharmacist thinking about medications for RSI. Know the kinetics of your induction agent and paralytic agents including onset and duration of the medications used. Also, know what to expect from the medications used.
        B
        • Breathing:
          • if the team thinks your patient has a pneumothorax and a chest tube is imminent, be ready for local analgesia or possible IV systemic analgesia for patient comfort
        C
        • Circulation:
          • If the patient is found to be hypotensive while circulation is being assessed, think adjuncts to blood product replacement.
          • Any patient in the trauma bay who is hypotensive and tachycardic is in hemorrhagic shock until proven otherwise.
          • These patients will get blood. This includes getting ready to administer calcium to patients receiving multiple rounds of blood products as hypocalcemia may develop due to citrate toxicity.
          • For traumas that present early, plus/minus TXA, and if your patient is on anticoagulation, reversal strategies based on what your patient was taking.
        D
        • Disability:
          • Think of traumatic brain injury and if present, Ruben anticipates the need for hypertonic saline or mannitol. He generally prefers 3% hypertonic saline as it does not affect hemodynamics and it is easier to get ready versus mannitol.
        E
        • Exposure:
          • Finally, the patients are exposed, this is when Ruben thinks ahead about antibiotics for open fractures and of course, life-saving tdap.
        What is a Secondary Survey?

        An

        AMPLE secondary survey should be taken and includes (ample being the operative
        term):

        • A – Allergies
        • M – Medication History
        • P – Past illness/pregnancy
        • L – Last meal
        • E – Events/Environment related to injury

        What parts of the Secondary Survey are pharmacists involved in?

        Pharmacists play an integral role in obtaining allergies or past medication history such as myasthenia gravis where certain medications are contraindicated

        • A medication history may also be obtained from these patients.
        Hemorrhagic resuscitation and pharmacist involvement

        Pharmacists have an integral role in MTP.

        • Electrolyte Disturbances
          • Being prepared for complications associated with MTP are key aspects in the management of trauma patients receiving multiple blood transfusions.
          • These patients may suffer from hypocalcemia due to citrate toxicity.
          • Citrate located in blood products may bind with calcium, causing hypocalcemia.
          • Be ready with calcium replacement. Patients may also have hyperkalemia as a complication from MTP due to the age of the PRBCs used rate of infusion, underlying renal failure, and severe tissue injury.
          • Classic EKG changes associated with hyperkalemia such as peaked T waves may be present.
          • This should be treated similarly to other conditions that cause hyperkalemia.
        • Anticoagulation Reversal
          • Patients who are on oral anticoagulation present unique challenges.
          • At Rubens’s shop, They have developed an order set that helps streamline the ordering of anticoagulation reversal strategies based on the medication the patient was taking prior to presentation.
          • Kcentra is our reversal strategy for both VKA (including vitamin K) and factor Xa inhibitors (sorry Andexxa) and we use idarucizumab for dabigatran reversal +/- FEIBA.
          • Ruben’s role is ensuring the correct doses are ordered, and then expedited to the patient’s bedside.
          • Also, Ruben provides education to the receiving nurse on how the medication should be administered.
        Pharmacists involvement with antibiotics with an open fracture
        • Pharmacists are integral in choosing the appropriate antibiotic for patients that present with open fractures.
        • This includes choosing the correct agent based on the type of open fracture (extremity vs. jaw. vs. skull), and environment (ex. aquatic traumas). Clarifying allergies prior to medication administration is another place that pharmacists have a role.
        • This includes choosing the correct agent based on the type of open fracture (extremity vs. jaw. vs. skull), and environment (ex. aquatic traumas). Clarifying allergies prior to medication administration is another place that pharmacists have a role.
        • Living in Miami, almost everyone says they have a penicillin allergy.
          • Letting the team know that you may use a third-generation cephalosporin routinely in this patients population and that it is safe as the R-side chains are different and there is little to no cross-reactivity (thank you, Bryan Hayes!).

        Pharmacist involvement with pharmacologic agents in TBI
        • If suspecting TBI, Ruben generally goes for hypertonic saline.
        • In these situations, I recommend a 250 mL bolus of 3%.
        • I like it better cause I can give it fast, don’t have to worry about hemodynamic effects, and do not need a 0.2-micron filter like with mannitol.
        • Another aspect of care for these patients is if they are intubated, ensuring they receive appropriate sedation and analgesia post-intubation.
          • This will help with ICP management.
        Ruben’s advice for new ED pharmacy practitioners responding to traumas that didn’t train at a trauma center?

        Be open to learning new aspects of care you did not learn at your previous hospital.

        Learn from your nurses and physicians leading the traumas. Do the little things (get blankets, help expose, etc.) and show up for every trauma.

        Show them how much you care, and the team will appreciate and value how much you know.

        Ruben’s Most Interesting Cases
        • There are so many!!!
        • There was an MVC where the patient needed an emergency cric, then placed on ECMO
        • Another was a truck driver who was on dabigatran and we used idarucizumab and FEIBA
        • Another was a boat propeller injury where I held the patient’s legs (still attached) and provided antibiotic recommendations due to the saltwater exposure.
        • Also, a couple of shark bites.
        References
        • Hopkins TL, Daley MJ, Rose DT, et al. Presumptive antibiotic therapy for civilian trauma injuries. J Trauma Acute Care Surg. 2016 Oct;81(4):765-74.
        • Scarponcini TR, Edwards CJ, Rudis M, et al. The role of the emergency pharmacist in trauma resuscitation. J Pharm Pract. 2011 Apr;24(2):146-59.
        • Patanwala AE. Pharmacist’s activities on a trauma response team in the emergency department. Am J Health Syst Pharm. 2010 Sep 15;67(18):1536-8.
        • Amini A, et al. Effect of a pharmacist on timing of postintubation sedative and analgesic use in trauma resuscitations. Am J Health Syst Pharm. 2013 Sep 1;70(17):1513-7
        •  Lane JE, et al. Current Concepts of Prophylactic Antibiotics in Trauma: A Review. Open Orthop J. 2012; 6: 511–517.
        • Montgomery K, et al. Pharmacist’s impact on acute pain management during trauma resuscitation. J Trauma Nurs. 2015 Mar-Apr;22(2):87-90.
        • Rossaint R, et al. The European guideline on management of major bleeding and coagulopathy following trauma: fourth edition. Crit Care. 2016; 20: 100.
        • Morrison JJ, et al. Military Application of Tranexamic Acid in Trauma Emergency Resuscitation (MATTERs) Study. Arch Surg. 2012 Feb;147(2):113-9. 

        The post Episode 11: The Role of an ED Pharmacist as Part of the Trauma Team with Ruben Santiago, Pharm.D., BCPS, BCCCP appeared first on The Pharm So Hard Podcast.

        30 min
      • Episode 10. Formulary Management with Oscar Santalo
        Definitions
        1. Formulary medication – A determination that the medication is “appropriate for routine use” in select patient populations
          1. Per 2008 ASHP Guidelines on the Pharmacy and Therapeutics Committee and the Formulary System
        2. Pharmacy and Therapeutics (P & T) Committee – establishes policy development, communication, education, and formulary management
        Background
        1. How most hospital/health systems define formulary is: product readily available or stocked in the pharmacy
        2. The environment surrounding hospital pharmacies has changed dramatically. The cost of pharmaceuticals, the types of newly approved medications for specific disease states, and the stipulations related to the reimbursement or procurement of medications have all been significantly altered.
        3. Medication Use Evaluations or Drug Utilizations Reviews are a formal process that aid in the evaluation of medication formulary decisions
        4. When evaluating a drug for formulary addition, the following factors need to be taken into account:
          1. Procurement and regulatory restrictions, economic considerations, safety & regulatory risks
        Major End Points
        1. Factors influencing formulary management decisions
          1. Cost, reimbursement, availability, specialization of medications (niche)
        2. Can have different sub-committees roll into or feed up to P&T
          1. Subcommittees include medication safety, quality, antimicrobial stewardship, adverse drug reaction, biotechnology subcommittee
        3. Instead of having formulary and non-formulary designations, we can expand this to include:
          1. Formulary, stocked
          1. Formulary, not stocked (or not consistently stocked)
          1. Formulary, restricted
          1. Formulary, requirement for confirmation of benefits of coverage prior to use
          1. Formulary, outpatient (or clinic) use only
          1. Non-formulary, stocked
          1. Non-formulary, not stocked
        4. Post formulary decision implementation strategy plays a significant role in deciding the success or failure of that formulary decision
          1. It is equally important as the building up towards the P&T Process
        References

        Heindel GA, McIntyre CM. Contemporary challenges and novel strategies for health-system formulary management. Am J Health Syst Pharm. 2018 Apr 15;75(8):556-560. 

        Leonard MC, Thyagarajan R, Wilson AJ, et al. Strategies for success in creating an effective multihospital health-system pharmacy and therapeutics committee. Am J Health Syst Pharm. 2018 Apr 1;75(7):451-455

        The post Episode 10. Formulary Management with Oscar Santalo appeared first on The Pharm So Hard Podcast.

        28 min
      • Episode 9: The Treatment of Symptomatic Hyponatremia with Hypertonic Saline with Jimmy Pruitt
        Case Presentation
        • TF is a 58-year-old 50 kg female that presented to the ED with a chief complaint of progressively worsening weakness and fatigue over the past day since ingesting MDMA (Ecstasy) and increased fluid intake over last 24 hours. During the physical exam, TF started to have tonic-clonic seizures that lasted 2 minutes. The ED resident orders POC labs and the Na+ came back at 118 mEq/L.

         How do you treat this symptomatic hyponatremia?

        Introduction
        • Hyponatremia is defined as any serum sodium
        < 135 mEq/L.
      • Severe symptomatic hyponatremia typically
      • occurs at a serum sodium < 120 mEq/L though the rapidity of the change in
        sodium is a key factor in the development of symptoms
      • Hyponatremia occurs in ~4% of adult patients
      • that present to the ED
        Signs and Symptoms
        • Mild/moderate Hyponatremia
          • Headache
          • Nausea/vomiting
          • Muscle cramps
          • Lethargy
          • Restlessness
        • Severe Hyponatemia
          • Disorientation
          • Focal neurologic deficits
          • Seizures (Status epilepticus common)
          • Coma
         SYMPTOMATIC HYPONATREMIA MANAGMENT
        • Often requires prompt correction
          • Fluid restriction and intravenous hypertonic
        saline
        • Reversible causes of hyponatremia corrected
        • Sodium deficit can be calculated to estimate
        replacement needs:
        • – Sodium deficit (mEq) = TBW x (desired Na –
        measured Na concentration)
        • TBWMEN = 0.6 L/kg x weight in kg
        • TBWWOMEN= 0.5 L/kg x weight in kg
        • May use adjusted body weight in obese
        • Treat neurologic emergencies with hypertonic saline
          • Hypertonic Saline 3%
            • 100-150 ml or 2ml/kg  over 10-30 minutes through a central OR peripheral line
          • Provide up to two additional 100-150 mL boluses, spaced 20 minutes apart, until a 5 mmol/L increase in sodium concentration is reached
        • Rapid correction of serum sodium by 2-3 mEq/L
        typically results in correction of neurologic emergency (particularly status
        epilepticus)
        • If symptoms do not improve continue IV 3%
        hypertonic saline at a rate leading to an increase of 1 mmol/L/hr.
        • This rate depends on each patient’s weight and
        percentage body water (see appendix for formula and example calculation)
        • Monitor sodium concentration every 4 hours
      • Do not exceed an increase of more than 10
      • mmol/L in 24 hours.

        Alternative Therapy
        • 50 cc of 8.4% sodium bicarbonate (1 “ampule”
        of crash cart bicarb) q20-30 x 3 if symptoms do not improve
        What About the Osmolarity of Hypertonic Saline?
        Pharmacologic Agent
        Osmolality
        3% NaCl
        1027 mOsml/L
        5% NaCL
        1711 mOsm/L
        7.5% Nacl
        2,567 mOsm/L
        8.4% Sodium bicarbonate
        2000 mOsm/L
        23.4% Nacl
        8011 mOsm/L
        D50W
        2,525 mOsm/L
        Etomidate
        4,900 mOsm/L
        Data For Use of 3% Hypertonic Saline Through a Peripheral Line
        • PMID 15026402
        • PMID 7511708
        • PMID 30745195
        • PMID 28471928
        • PMID 23283268
        • https://emcrit.org/squirt/peripheral-hypertonic-saline-safe/
        Protocols for 3% Hypertonic Saline

        https://www.uwhealth.org/cckm/cpg/medications/Peds-IV-Administration-CPG—January-2018.pdf

        https://www.universityhealthsystem.com/~/media/files/clinical-pathways/hypertonic-saline-2018.pdf?la=en

        http://vcportal.ventura.org/VCHCA/Hospitals/Medical%20Staff%20Services/CPG/hypertonic-saline-practice-guideline-4-2011.pdf

        Pharmacy Related Considerations
        • Is there a protocol that guide the use of 3% NaCl for Symptomatic Hyponatremia?
          • Is the language clear on the recommendation on the type of line required vs recommended?
          • Is the protocol for ICP management?
          • Is the protocol for Hyponatremia?
        • Verifying 3% NaCl in the ED
          • A quick look at labs
          • The nursing note may have info about symptomatic hyponatremia
          • Quick Lit search if uncertain and no one to consult with
            • Institution guidelines, Tintinalli’s, Rosen’s, Uptodate, Pubmed, Societal Guidelines
          • When reaching out to team ask questions and be ready with a therapeutic alternative
        • 3% Hypertonic Saline through Peripheral Line?
          • Should be through a central line if one is available, however, 3% can and should be bolus on IV smart pump through a large Bore IV
        • Is 3% NaCl in your institutional automatic dispense cabinet? If not why? If not how quickly can it be obtained?
        Nursing Considerations
        • Ask for clarification from experience nurse, pharmacist, and provider if there is confusion as to what is being asked of you and is this treatment appropriate
        • Be aware that this is a time-sensitive matter and newer healthcare professionals may be uncomfortable explaining why there’s confusion on the treatment plan
        • 18 G IV in the most distal access point
        • IV pump, pump tubbing, and no need for a filter, and have dedicated line for hypertonic initially
        • Nursing note with communication from Provider and description of what the symptoms of symptomatic hyponatremia
        Physician Considerations
        • Clear communication about what you need the
        patient to receive
      • Realize that you may be the only one who’s
      • comfortable with the treatment and let this be a teaching moment vs a screeching
        moment
      • Consider what labs can be done as a point of
      • care (POC) and what labs need to be sent for go pass off to your consultant
      • Put in your CPOE order comment that “3% NaCl is
      • for symptomatic Hyponatremia. Bolus required”
        • Helps pharmacy see whats it for and prompt quick
        lit search
        Adverse Reactions
        • Rapid
        overcorrection of serum sodium can cause osmotic demyelination syndrome
        (ODS)
        • ODS
        can manifest as ataxia, quadraplegia, CN palsies or “locked-in” syndrome
      • Can
      • occur up to 7 days after rapid correction
      • Preventing
      • overcorrection
        • Do
        not increase serum sodium by more than 6-8 mEqL in the 1st 24 hours
      • Fluid
      • restrict patient after relief of neurologic emergency
      • Monitor
      • urine output (UO): If UO > 100 ml/hr, send urine osmolarity + urine
        sodium
      • Urine
      • osmolarity < 100, give DDAVP 1 mcg
      • Correct
      • Hypokalemia
        • Often
        will see hypokalemia in patients with severe hyponatremia
      • Correction
      • of hypokalemia can improve hyponatremia
      • Oral
      • repletion safe and efficacious if patient tolerating oral intake
        Pharmacy Friday Pearls Handout
        3-Hypertonic-Saline_NaCL-for-Symptomatic-Hyponatremia-Pharmacy-Friday-Pearls-Jlp1-1

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        Related FOAM Posts

        EMCrit

        • https://emcrit.org/emcrit/hyponatremia/

        CanadianEM

        • https://canadiem.org/hyponatremia-in-the-ed/

        Emergencymedicinecases

        • https://emergencymedicinecases.com/episode-60-emergency-management-hyponatremia/

        EmDoc

        • http://www.emdocs.net/core-em-severe-hyponatremia/

        Pulmcrit

        • https://emcrit.org/pulmcrit/emergent-treatment-of-hyponatremia-or-elevated-icp-with-bicarb-ampules/
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      • Perez CA et al. Complication Rates of 3%
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      • Meng L et al. Association between continuous
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        The post Episode 9: The Treatment of Symptomatic Hyponatremia with Hypertonic Saline with Jimmy Pruitt appeared first on The Pharm So Hard Podcast.

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