Skip to content

Evan Kuhl, MD

January 30, 2017

A recent article in The British Medical Journal highlights the impact of a web based aid to help in the decision for either admission for observation or referral for outpatient workup in those with chest pain.  Low-risk chest pain patients are frequently admitted for observation and further testing because it is sometimes difficult to predict which patients are at risk for acute coronary syndrome and sudden death.  Sometimes patients are admitted to the hospital even when risk is very low. The article, “Shared decision making in patients with low risk chest pain: prospective randomized pragmatic trial” by Hess et al found that when a shared decision aid was used for them to understand this risk and make their own decisions about admission, patients not only had greater knowledge of their risk for acute coronary syndrome and options for care, but also preferred outpatient follow-up to admission1. Dr. Hess’s results were noted in the most recent SAEM Academic Emergency Medicine Consensus Statement on shared decision making as one of the few ED-based publications on shared decision making2.

The study took place in six emergency departments across the US where adult patients presenting with the chief complaint of chest pain were considered for inclusion. Patients were excluded if they had ischemic changes on ECG, an initial troponin greater than the 99th percentile, had known coronary artery disease, recent cocaine use, or had prior cardiac interventions or admissions. For patients in the treatment group, the treating physician used an online tool to determine the pretest probability of acute coronary syndrome. This web-based tool, previously recognized by in a 2014 Circulation article, utilizes ECGs, troponin results, and the patient’s age, sex, and risk factors to help determine the pretest probability for acute coronary syndrome3. The physician then presented the patient with the decision aid and educated the patient on the test results and potential need for observation or further outpatient workup. Together, a shared decision was made between the patient and physician regarding disposition.

The primary outcome of this study was patient knowledge (tested with knowledge-based questions), while secondary outcomes centered on the degree of uncertainty patients experience when making a choice. This was determined by using a decisional conflict scale, which scores 16 individual items to determine certainty patients feel when deciding which treatment option to take. Overall, 3,236 patients were assessed for eligibility from 2013 to 2015, with a total of 913 patients enrolled, and the authors collected follow-up data for 92.2% of patients.

This study found that those patients presented with the decision aid had greater knowledge (tested by questions about their 45-day risk of ACS and knowledge about ACS) and significantly less decisional conflict. More patients in the decision aid group opted for outpatient testing than the control group (30.2% vs 17.2%). The rate of coronary revascularization, admission to hospital, readmission or repeat emergency department visits did not differ between the groups.

Patient-centered care was first coined in 1988 to emphasize the need to shift the focus of modern medicine aware from disease and back to the patient. Shared decision making provides the patient with better understanding of proposed therapies, while the physician gains insight into the patient’s values and goals. When there are multiple options supported by evidence, shared decision making tools help determine the best option for each patient. In the current medical environment, many physicians may feel pressed to admit patients with what is typically considered “low risk” chest pain because of an assumed patient preference for maximum treatment and intervention. When patients have minimal knowledge about a disease process and physicians are concerned about potential medical and legal effects of a missed diagnosis, there is a lower threshold for further testing and admission. This is estimated to result in approximately $7 billion in unnecessary hospitalizations, false-positive tests, and invasive investigations. Shared decision making tools such as the one tested in this study not only increase patient knowledge and decrease their decisional conflict, but can also decrease admissions and overuse of medical resources. The shift in patient care to better incorporate patient preferences can safely allow for more responsible resource utilization while providing safe and appropriate outpatient follow-up.

 

 

References:

1.         Hess EP, Hollander JE, Schaffer JT, et al. Shared decision making in patients with low risk chest pain: prospective randomized pragmatic trial. BMJ 2016;355:i6165.

2.         Grudzen CR, Anderson JR, Carpenter CR, Hess EP. The 2016 Academic Emergency Medicine Consensus Conference, Shared Decision Making in the Emergency Department: Development of a Policy-relevant Patient-centered Research Agenda May 10, 2016, New Orleans, LA. Acad Emerg Med 2016;23:1313-9.

3.         Kline JA, Jones AE, Shapiro NI, et al. Multicenter, randomized trial of quantitative pretest probability to reduce unnecessary medical radiation exposure in emergency department patients with chest pain and dyspnea. Circ Cardiovasc Imaging 2014;7:66-73.


Evan Kuhl, MD is an Emergency Medicine Resident at The George Washington University Hospital

Ameer Khalek

January 26, 2017

A new article by Nagurney et al. in press in the Annals of Emergency Medicine examined association between emergency department (ED) visits and functional decline in the community-living geriatric population. The study found that although not as debilitating as an acute hospitalization, ED visits that do not result in hospitalization are still associated with clinically significant decline in functional status within 6-months of the visit.

From a cohort of 754 community-living older persons across up to a 14-year span, the team matched 813 ED visits without hospitalization (ED-only) to 813 observations without an ED visit (control). The mean participant age was 84 years. Disability was measured by data collected on demographic characteristics, chronic conditions, body mass index, cognitive impairment, depressive symptoms, and physical frailty. After a 6-month follow-up period, the ED-only group had a significantly higher disability score than the control (adjusted risk ratio: 1.14). Furthermore, both nursing home admissions and mortality rates were higher between the two groups (3.11 and 1.93, respectively). Considering that even a relatively minor issue may be a flag for functional decline and additional resources on both preventive and corrective fronts, effective screening and demographic-specific acute care is crucial.

As a nexus between inpatient and outpatient care, the ED has a major role in improving care coordination and allocation of resources to the geriatric population. The American College of Emergency Physicians (ACEP) recognizes the heterogeneity of this demographic, and one solution to Nagurney et al.’s findings is proper dissemination and implementation of the Geriatric Emergency Department (GED). GED’s are designed to address specific needs of the older population with associated benefits such as improved healthcare outcomes and a reduction of unwarranted hospitalizations/readmissions. One effective pillar is the utilization of an interdisciplinary team to address symptoms that are typical of and unique to geriatric patients. A holistic approach through advanced care coordination between a medical team, social workers, pharmacists, and physical therapists allows various metrics of care to be addressed (e.g., home health services, assessment of patient gait, and pharma-compliance).

In a podcast with Urgent Matters, Drs. Ula Hwang & Kevin Biese of the Geriatric Emergency Department Collaborative (GEDC) describe in detail the opportunity for GED development in terms of care coordination and safely preventing avoidable hospitalizations.  Dr. Hwang describes the ability for “[GED] on-site assessments to screen for delirium, cognitive dysfunction, depression, and check what their needs are in the home.” All patients are given follow-up calls starting at 24-48 hours and subsequent regular intervals to assure a successful transition to the outpatient setting (regardless of hospitalization status). The team-driven, simple screening approach to prevent poor outcomes and improve ED experience for the geriatric patient is evidence-based (e.g., Karam et al., McCusker et al.). Looking forward, the future should focus on prevention of reducing functional decline, iatrogenic problems, and improving effective care throughout the healthcare continuum.

The US Census shows that over 40 million Americans are 65+, and that the population of 85+ are now the fastest growing. Dr. Terry Filmer, president of the John A. Hartford Foundation (a major supporter of initiatives to improve healthcare for older adults), states that there are currently over 100 GED’s in the United States - a rapidly increasing number to meet the demand.

St. Joseph’s Regional Medical Center designed a GED program – click here to learn more about their implementation and protocol-specific information from the Urgent Matters Toolkit.


Ameer Khalek is a MPH student at the GWU Milken Institute School of Public Health

Evan Kuhl, MD

November 2, 2016

Last month, Health Affairs published new research on hepatitis C treatment in American prisons. Hepatitis C is a liver disease and the most common bloodborne pathogen in the United States, infecting approximately 1 percent of the general population.(1) Within the prison population, however, the prevalence of hepatitis C is higher: 17 percent. Prisoners are a key demographic to decrease the spread of hepatitis C, which is spread through IV drug abuse because approximately 20-55 percent of inmates have used IV drugs in the past.

The article is the most recent investigation to identify the number of inmates with hepatitis C, and identify how these people are being treated. This is important now because today hepatitis C is treatable through direct-acting antivirals (DAAs). Treatment is important because hepatitis C can lead to cirrhosis, portal hypertension and chronic liver failure requiring liver transplant. The DAAs are very expensive with a 12-week course costing $43,418-$94,500. Yet 90% of the time, the treatment is curative, preventing the morbidity associated with chronic hepatitis.

The main finding of the article was that despite the drugs being available and effective, less than 1 percent of known infected inmates actual receive treatment. This is despite US Supreme Court rulings that prison officials must provide adequate medical care of inmates, and the Federal Bureau of Prisons’ Clinical Practice Guidelines recommend the use of DAAs. Currently, prisoners in Massachusetts are suing the state for withholding treatment.(2) On average, each state spent about 6 percent of their annual drug budget on hepatitis C medications: $39.8 million annually. This is despite the fact that many states actually negotiate lower prices.

Clearly, cost plays a major role in this failure to treat inmates with DAAs. However, other reasons cited by the authors include outdated treatment guidelines which do not take into account DAA availability.  As of January, 1st, 2016, Tennessee’s treatment guidelines did not recommend DAA medications, and only recommended hepatitis C testing for inmates meeting certain indications, unless specifically requested by an inmate. In addition, state protocols only recommend treatment for those with more severe disease, including cirrhosis.

In the Health Affairs article, the authors describe several ways to increase treatment and decrease costs. First, the federal 340B Drug Discount Program allows health institutions to partner with prisons and provide healthcare services including hepatitis C treatment, a system being used by three of the four departments paying the least for DAAs. Pooled procurement of DAAs is also recommended, as currently many departments negotiate independently for drug prices. Finally, increased federal involvement and funding is needed help treat inmates. Once inmates are released, the federal government bears a significant proportion of the cost of hepatitis C, which is much higher if it’s untreated. Treatment in an institutional setting may provide greater savings and more effective treatment, while treating those at the highest risk of spreading the disease. This article is a first step towards understanding the burden and availability of effective treatment for one of the most high-risk populations in the United States.

 

1. Beckman AL, Bilinski A, Boyko R, et al. New Hepatitis C Drugs Are Very Costly And Unavailable To Many State Prisoners. Health Aff (Millwood) 2016;35:1893-901.

2. Loftus P. Prisoners Sue Massachusetts for Withholding Hepatitis C Drugs. The Wall Street Journal 2016 Jun 11, 2015.


Evan Kuhl, MD is an Emergency Medicine Resident at The George Washington University Hospital

Evan Kuhl, MD

October 13, 2016

New data published this summer studies medical marijuana trends in the United States. Specifically, one article published in Health Affairs and written by Ashley and David Bradford of the University of Georgia reviews how medical marijuana availability has impacted other prescriptions filled by Medicare Part D enrollees1. The study, also noted in the BMJ, found there were several categories where prescriptions where reduced2. On average, states with medical marijuana saw a 20% decrease in prescription medications for spasticity, and an 8-13% decrease in medications for anxiety, depression, nausea, psychosis, and sleep disorders. The decrease in prescription drug use saved an estimated $165.2 million in Medicare funds in 2013 alone. If medical marijuana was available nationwide, the authors estimated that Medicare could see a 0.5% reduction of the program’s nation-wide spending.

 

Overall, this decrease in prescription drug utilization saved approximately $165.2 million in Medicare funds in 2013 alone.

 

While the Bradford study shows that marijuana appears to be replacing several other medications, the question is whether marijuana actually as effective as other drugs? The answer is that several randomized clinical trials data support the effectiveness of marijuana , some researchers question the standards used to evaluate how well it really works. For example, research has examined how marijuana helps gastrointestinal conditions, such as Crohn’s disease3.  Yet, most of this research evaluates subjective responses to marijuana, and do not focus on objective disease markers such as intestinal inflammation or C-reactive protein levels.  Therefore, even if patients using marijuana note pleasurable side-effects of the drug as effective treatment, it may not directly impact the disease process itself.  Dartmouth Drs. Koliani-Pace and Siegel co-authored an article calling for increasing the quality control of marijuana research. They wrote: “If marijuana can meet all of the FDA requirements, including efficacy data, evidence of safety, and a meticulous quality control program, then the medicinal use of marijuana could be supported”3. Besides objective outcome data, other major concerns still left unanswered include the untoward respiratory side effects of marijuana smoke, as well as the co-use of marijuana and tobacco, with some research showing that marijuana use can increase tobacco use and dependence4.

Currently, 39 states now allow medical marijuana despire still being listed as a Schedule 1 drug by the Federal government. Although individual state regulations vary, every program requires a physician to prescribe the use of marijuana or marijuana-derived substances. As the policies and regulations regarding marijuana continue to change, it will be essential to continue researching both the efficacy of marijuana treatment and the impact on healthcare utilization.  As providers, it is important to understand the impact these policies on our patients. The research and experience of providers is an important part of creating safe and viable policies to protect and treat our patients.

 

1.         Bradford AC, Bradford WD. Medical Marijuana Laws Reduce Prescription Medication Use In Medicare Part D. Health Aff (Millwood)                     2016;35:1230-6.

2.         Dyer O. US states that allow medical marijuana see drop in prescriptions for other drugs, study finds. BMJ 2016;354:i3942.

3.         Koliani-Pace J, Siegel CA. Is the Hype of Medical Marijuana All Smoke and Mirrors? Am J Gastroenterol 2016;111:161-2.

4.         Wang JB, Ramo DE, Lisha NE, Cataldo JK. Medical marijuana legalization and cigarette and marijuana co-use in adolescents and                       adults. Drug Alcohol Depend 2016;166:32-8.


Evan Kuhl, MD is an Emergency Medicine Resident at The George Washington University Hospital

Ameer Khalek

October 10, 2016

Triage is the process of determining treatment priority based on the severity of a patient’s condition. The term triage is derived from the French word trier which means “to sort.” The concept of triage was first applied to medicine by French military surgeon Baron Dominique-Jean Larrey, a chief surgeon of Napoleon’s Imperial Guard. Larrey recognized the need to categorize the wounded during battle to treat and evacuate those requiring the most urgent medical attention (Iserson et al.). While medical technologies advance and the time-sensitive nature of emergencies stay the same, it is important to continually revise triage systems to fit local needs and resources.

Currently, the most common emergency department (ED) triage system in the United States is the Emergency Severity Index (ESI). The ESI is a five-level tool for experienced ED personnel to rate patient acuity which takes into consideration both clinical and operational decisions such as resource allocation. In a recent study by Khan et al., a new triage system is proposed that better matches the needs of austere environments. In her podcast with Urgent Matters, Dr. Khan described the many reasons why traditional triage systems are not as useful where there are fewer experienced emergency providers and a scarcity of resources, such as in low- and middle-income countries. Low- and middle-income countries can’t afford to have experienced providers conduct triage assessments because they are needed for patient care, and the resource-based triage in the ESI is not as relevant when there are fewer resources available. For example, providers in austere settings may not have the ability to order certain radiography or laboratory tests.

Khan and her team proposed the one-two-triage (OTT) system. OTT is a two-triage system that can be reliably applied after only eight hours of training. Instead of relying on experience in making subjective clinical decisions, Stage 1 is designed to quickly separate out patients categorized as critical (red) and emergent (orange) from a simple assessment of the patient’s airway, breathing, circulation, and disability. Patients are greeted and pulse oximetry is assessed. If the patient does not qualify as critical or emergent, they are sent to registration. Stage 2 separates patients into urgent (yellow) or non-urgent (green) based on their chief complaint and vital signs, taking the person who is conducting triage – who may have little medical training – through a series of protocols related to each chief complaint to determine how emergent a specific condition might be. This allows less experienced providers to assess severity of illness based on medically sound algorithms. The complete OTT process can be found here.

OTT is currently being used as an alternative to ESI in 22 Cambodian hospitals (with 21 additional EDs coming on board soon), a healthcare population where there is a relative paucity of experienced healthcare professionals. As Dr. Khan discussed in her podcast, crowd-sourcing information about triage needs in specific settings can catalyze the process of customizing systems in various environments. For more information, you can reach out to her here. 


Ameer Khalek is a MPH student at the GWU Milken Institute School of Public Health

Will Denq, MD

October 6, 2016

Emergency physicians commonly use a combination of history, physical exam, EKG, labs, and imaging to help diagnose congestive heart failure (CHF) in the emergency department in patients who present with shortness of breath. However, sometimes it can be confusing and what initially looks like heart failure ends up being something else, such as pneumonia (1-3). Misdiagnosis can have real consequences, particularly when diuretics used to improve CHF result in worsened conditions such as a pulmonary embolus or other serious pathologies.

In a recent paper, Basset et al derived and validated a CHF clinical prediction rule called the Brest score (4) which is intended to improve the accuracy of a heart failure diagnosis in ED patients. They looked at 927 undifferentiated dyspneic patients in their ED to create it and externally validated it in 206 patients. The score relies on 11 variables based only on history, physical, and EKG to risk stratify patients into low, intermediate, and high probability groups.

The prevalence of confirmed CHF patients was 6.7% in the low probability group, 58% in the intermediate, and 91.5% in the high. The authors argue that these results are accurate enough when weighing risks and benefits to begin early treatment in the high risk group. Unlike many diagnoses made in the ED, a healthcare provider using this score may not necessarily have to wait for labs or radiology results to initiate management. On the other spectrum, with so few CHF patients in the low risk group, patients who are low risk by the Brest score should prompt the provider to search for other etiologies of dyspnea.

There were several limitations of the paper. The score still needs a prospective impact analysis validation, it was from a single center, and several pathologies may coexist in a single patient. Although the risk-benefit ratio skews towards treatment in the high risk group, the subsequent management of CHF is not benign especially in volume-depleted patients.

The Brest score represents an interesting adjunct in the early diagnosis of CHF in the undifferentiated dyspneic ED patient. With time being an important factor in management and disposition of CHF, the score stands alone in quickly risk stratifying the patient without waiting for labs or radiology results. Other CHF decision rules, such as the Boston criteria (5), Steingart and PRIDE (6,7) decision tools, rely on time-delaying lab results such as BNP or radiology results such as a CXR. The Framingham (8) and Gothenburg (9) scores were epidemiologic studies and utilize certain factors that are not readily obtainable at the bedside.

Along with decision rules, other data at the bedside can be helpful to diagnose CHF, such as lung ultrasound.  A 2015 multi-center prospective study (n=1005) by Pivetta et al demonstrated a significantly higher accuracy than all other standards when using the clinical evaluation and bedside lung ultrasound. Sensitivity was reported at 97% with specificity being 97.4%. Perhaps a completely validated Brest score could improve the diagnosis when used in conjunction with lung ultrasound and move away from using data such as BNP or chest xray. It could result in an accurate, bedside diagnosis that does not rely on labs or imaging. Although not ready for prime time, it could significantly increase the accuracy of CHF diagnosis and accelerate management in the undifferentiated dyspneic ED patient.

Brest score:

Variables

Points (+2)

Age > 65

1

Anamnesis variables

Sudden dyspnea

2

Onset of symptoms at night

1

Orthopnea

1

Risk Factor variables

Prior CHF episode

2

Myocardial infarction

1

Chronic pulmonary disease

-2

Clinical Examination variables

Pulmonary crackles

2

Pitting leg edema

1

EKG Abnormality variables

ST segment abnormalities

1

Atrial fibrillation/flutter

1

Max score

15

 

Low Risk: ≤ 3

Medium Risk: 4 - 8

High Risk: ≥ 9

The Brest score starts automatically with 2 points – perhaps a superstitious move by the authors to avoid an unlucky total of 13 points.

References:

  1. Remes J, Miettinen H, Reunanen A, Pyörälä K. Validity of clinical diagnosis of heart failure in primary health care. Eur Heart J 1991;12:315–21.
  2. Fuat A, Hungin AP, Murphy JJ. Barriers to accurate diagnosis and effective management of heart failure in primary care: qualitative study. BMJ 2003;326:196.
  3. Ansari M, Massi BM. Heart failure: how big is the problem? Who are the patients? What does the future hold? Am Heart J 2003;146:1–4.
  4. Basset A, et al, Development of a clinical prediction score for congestive heart failure diagnosis in the emergency care setting: The Brest score, Am J Emerg Med (2016), http://dx.doi.org/10.1016/j.ajem.2016.08.023
  5. Schocken DD, Arrieta MI, Leaverton PE, Ross EA. Prevalence and mortality rate of congestive heart failure in the United States. J Am Coll Cardiol 1992;20:301–6.
  6. Baggish AL, Sieber U, Lainchbury JG, Cameron R, Anwaruddin S, Chen A, et al. A validated clinical and biochemical score for the diagnosis of acute heart failure. The ProBNP Investigation of Dyspnea in the Emergency Department (PRIDE) Acute Heart Failure Score. Am Heart J 2006;151:48–54.
  7. Steinhart B, Thorpe KE, Bayoumi AM, Moe G, Januzzi Jr JL, Mazer CD. Improving the diagnosis of acute heart failure using a validated prediction model. J Am Coll Cardiol 2009;54:1515–21.
  8. McKee PA, Castel WP, McNamara PM, KannelWB. The natural history of congestive heart failure: the Framingham Study. N Engl J Med 1971;285:1441–6.
  9. Eriksson H, Caidahl K, Larsson B, Ohlson LO,Welin L,Wilhelmsen L, et al. Cardiac and pulmonary causes of dyspnoea–validation of a scoring test for clinical-epidemiological use: the Study of Men Born in 1913. Eur Heart J 1987;8:1007–14.

Will Denq, MD is an Emergency Medicine Resident at The George Washington University Hospital

Ameer Khalek

September 6, 2016

A key indicator of emergency department (ED) performance is length of stay (LOS), or how long a patient remains in the ED from the time they arrive until departure. Literature supports that adverse outcomes, decreased patient satisfaction, and ED crowding are concomitants of prolonged ED LOS. In the latest issue of The American Journal of Emergency Medicine, Dr. Shou-Yen Chen et al. discusses factors associated with prolonged ED LOS, focusing on mass casualty incidents (MCI).

A MCI is declared under any circumstance where the number of casualties exceeds the amount of available resources. Not too long ago, I participated as EMS Command in a planned active shooter drill on GW’s campus and experienced firsthand what a MCI might look like.  After this experience, I remained curious about how EMS triage and initiation of treatment translated to ED care in a MCI.

Dr. Chen’s study enrolled patients who were treated for the burn injuries during a MCI at Formosa Fun Water Park. The study identified various patient characteristics correlated to one of three Triage Levels (I – emergent, II – urgent, III – less urgent), and described for each of these groups the management in ED, registration before/after hospital MCI response activation, % total body surface area (TBSA) of partial or full thickness burns, etc. The number of patients stratified by triage levels was I: 14, II: 19, and III: 15.

Once the MCI response was activated at the receiving facility, researchers did not find a significant association between patient load and ED LOS. Interestingly enough, Dr. Chen’s examination of three phases following transfer of care from pre-hospital personnel revealed that (1) input and (2) throughput were solely based on the readiness of ED staff. However, (3) output was co-dependent upon the continuum of care – specifically the downstream availability of beds –  and scale of MCI response. According to the study, “the output time interval remained prolonged even after opening [a] reserved unit because of limited staff… identifying a cutoff value within the output time interval might be useful to determine the timing of reallocation of personnel/resources.” When efforts to continue advanced resuscitation warrant quick disposition, such as the intensive care unit, the resource-availability to manage that burden is the key aspect of decreasing ED LOS. Considering more than the capabilities of the receiving facility examined in the study, the approach applies to shortening all ED LOS under resource-constrained circumstances.

An earlier study by Dr. Asher Hirshberg et al. found that the concept of minimal acceptable care was the key to a staged management approach during an MCI. He also found that variable surge capacity was dependent on the rate of patient arrival, as opposed to the availability of beds. Therefore, the importance of recognition and initiation of MCI protocols is paramount for reducing crowding and maintaining a quality of care in the ED.

 


Ameer Khalek is a MPH student at the GWU Milken Institute School of Public Health

Ameer Khalek

August 10, 2016

Emergency Medical Technicians are trained to assess patient signs and symptoms and deliver specific, protocol-based treatments in the pre-hospital setting. While EMTs are not trained as diagnosticians, one common presentation we are trained to recognize and treat is hypoglycemia, or a low blood glucose level. Testing for hypoglycemia by EMTs in the field involves sampling blood – commonly through a finger prick – and testing the blood glucose level with a glucometer device. This approach to bedside sampling of blood where the result is available immediately is called point-of-care testing (POCT). POCT for blood glucose is very accurate with a specificity of 99.3%.  When patients have hypoglycemia, we as EMTs can often address the problem by administering sugar solutions or intravenous dextrose. However, beyond POCT for blood glucose, there are other ways that EMTs can use POCT to help patients. Below I describe several studies where EMS personnel have used additional POCT in useful ways.

A study by Guerra et al. examined the feasibility of EMS personnel recognizing an acute sepsis patient using venous lactate measures. Their study found that although there was a lack of EMS education on sepsis identification, mortality from severe sepsis decreased from 26.7% to 13.6% after the implementation of the protocol. While the reported treatment effect seems unfeasibly large, the authors concluded that by having a Sepsis Alert Protocol in place, both EMS and the ED personnel were able to initiate treatment in the early phases of illness.  Sepsis is a time-sensitive disease where earlier resuscitation and care can improve outcomes.

Another study by Venturini et al. examined the reliability of pre-hospital POCT for troponin levels, which can be useful to detect acute heart damage during heart attacks. They found no significant difference in whole-blood troponin results between those performed in the ED and in the moving ambulance (p <0.005). Immediate access to troponin results can aid in the diagnosis of acute myocardial infarction (specifically without ST-elevation). Stengaard et al. also predicts that pre-hospital POCT will be central in pre-hospital heart attack care in the near future.

Beynon et al. used pre-hospital POCT to examine whether the pre-hospital physician assessment of hemostatic parameters is feasible. Point-of-care INR testing was performed on a total of 103 patients, revealing a pre-hospital sensitivity of 100% and specificity of 98.7% for detecting coagulopathy. Furthermore, the median time saved through POCT compared to results being sent to a central lab upon transfer of care was 69 minutes (ranging from 33 to 336min) – substantially beneficial for patients with intracranial hemorrhage.

From the results of these studies, we see that POCT in the pre-hospital setting seems to be reliable, valid, and in many cases helpful to clinical care. Along with pre-hospital initiation of care, information relayed to a receiving facility can allow for the mobilization of resources to improve timely access to definitive care. As medicine moves from volume to value, there are many ways that EMS can contribute to a higher-value healthcare system. POCT is one, important way that is feasible and effective, but will require further EMS education and protocol development prior to widespread implementation.


Ameer Khalek is a MPH student at the GWU Milken Institute School of Public Health

Sonya Chistov

July 21, 2016

Major metropolitan city emergency departments (ED) are constantly inundated with drug and alcohol intoxications. These days, health care providers are noticing a new surge in consumption of “designer drugs”. As a professional working for some time in a Washington D.C. ED, I have personally seen the dramatic increase in synthetic cannabinoids abuse.

What Are Synthetic Cannabinoids?

Synthetic cannabinoids are a new class of synthetic molecules developed to mimic the naturally occurring, psychoactive component of marijuana: tetrahydrocannabinol (THC). THC naturally binds to endogenous cannabinoid receptors, CB1 and CB2, as partial agonists. The resulting interaction between THC and the CB1 receptor causes changes in perception, relaxation, body temperature, and hunger. In addition, THC has been implicated in providing relief to patients with chronic health issues such as wasting disease and chemotherapy-related emesis and nausea. Since the 1960s, cannabinoid research has focused on creating synthetic analogs of THC, with similar analgesic and anti-inflammatory properties, but without the psychoactive effects. However, some of the chemical structures synthesized act as full-agonists at the same CB1 receptor—increasing the inhibition of GABA neurotransmission and therefore, the severity of the psychoactive and physiological symptoms.

“Spice”, “K2” and “Smoke” are common names for products marketed as “incense”. They contain a mixture of natural herbal ingredients that are sprayed with these chemical analogs. The resulting product is marked as “not for human consumption”, which makes it difficult for regulators to control. In 2011, the Federal Drug Administration marked common synthetic cannabinoids (JWH-018, JWH-073, JWH-200, CP 47-497, and CP-47-497C8) as schedule I substances.  However, new synthetic derivatives and homologs with very similar effects are constantly being created, rebranded, and redistributed across the United States. These products are inexpensive and found in local gas stations, bodegas, and on the Internet, which makes them an easy drug to get and use.

What Does A “K2” Patient Look Like In The ED?

ED patients with acute synthetic cannabinoid intoxication may present with a variety of symptoms based on the type, dose and route of consumption. The most notable clinical presentations are either: A) sluggish and drowsy or B) severely agitated and aggressive. Drowsy patients can often present with bradycardia, hypotension, emesis, confusion, and frank unresponsiveness to verbal and physical stimuli. In cases of severe agitation and aggressiveness, patients may present with tachycardia, hypertension, hallucinations, or paranoid behavior, which can be disruptive to a busy ED. These patients sometimes require physical restraints, or chemical restraint, in the form of sedatives. For many patients that I’ve seen, consumption of synthetic cannabinoids is not always an isolated ingestions, but often times combined with alcohol or street drugs.

What are Synthetic Cannabinoids Doing to The Public’s Health and What Can Be Done?

The long-term consequences of prolonged synthetic cannabinoid use remains unclear. Though most of the medical interventions to treat synthetic cannabinoid intoxication is supportive, increased use and abuse of these products is already burdening EDs not inly in major cities, like DC, but around the country. in emergency medicine. Legislation combating the sale of products containing certain ingredients has already been put in place, manufactures simply create new products and distribute them as usual.

However, local communities are doing their part to warn citizens about the harmful effects of the drug. For example, in regions of Washington D.C., educational campaigns have placed advertisements of buses to warn the public of about the dangers of K2 and Spice. Unfortunately, until a broader solution is identified and implemented, healthcare providers in ED across the country will continue to see more and more visits in relation to this dangerous drug.


Sonya Chistov is an ED Technican at The George Washington University.

Evan Kuhl, MD

July 8, 2016

Elderly patients have the highest rate of ED usage amongst all adult populations as well as the highest return rate.  Despite this increased burden on the healthcare system, it is difficult to predict poor outcomes after discharge. We all want to treat each patient “as if they were my grandfather/grandmother” yet we still cannot prevent many catastrophic outcomes. Of course we know that many chronic diseases increase the risk of readmission, and the 1-year mortality of many injuries are very well studied—but translating these risks into improvement of patient care is difficult, and many patients don’t fall so neatly into these boxes. There is still a need to identify risk factors to help providers identify patients at high risk of poor or catastrophic outcomes.

A new article by Dr. Gelareh Gabayan et. Al takes a new perspective on this problem. Instead of identifying historical information, type of injury, or other clinical data that is classically used to highlight at-risk patients, the team instead looked at process-of-care factors which occurred during the ER visit. What are we doing during a visit that can raise a red flag? Their study generated 300 case-control visit pairs of patients >65 years old who were treated in their ED system, and either died or was admitted to the ICU within 7 days of discharge. The chart review matched 300 patients who experienced such an outcome with 300 case control patients who did not, then compared the charts to identify predictors for ICU admission and/or death. Read more about their methods of exclusion, randomization, and measurement in their article, here. The article identifies many characteristics as having an increased adjusted odds ratio for death or ICU admission, including Asian/Pacific islander, Hispanic, or black ethnicity, hypotension, tachycardia, and mental status changes.

Most interesting, however is that changing the disposition of a patient (or noting the consideration of admission) was found to be associated with a greater likelihood of death or an ICU admission. Change in disposition was the only association that was not a hard number. In fact, it’s the only association that we actively play a role in as physicians. Interestingly, Dr. Gabayan’s paper finds that when a change in disposition was related to specialty consultation, there was no longer an increase in risk. It appears these consults were able to provide services or follow-up care outside of an emergency physician’s scope of practice. Per the article; “Our findings, coupled with that of other studies, suggest that regardless of the initiating event causing the change in disposition status, the emergency providers’ clinical judgment about the disposition (admit versus discharge) of the patient should be given special attention by both the care team and the patient.”  Next time you consider your disposition of an elderly patient, take a moment and consider their next 7 days.

Interested in more? This month’s Annals of Emergency Medicine included several articles regarding the care of our elderly patients, including two other very interesting articles: Dr. Fassier’s article explores the attitudes of EM physicians regarding critically ill elderly patients, while Drs. LeFebvre and Platts-Mills provide an editorial to the article, including discussing the frustrations many EM physicians have when it comes to both the patient and family.


Evan Kuhl, MD is an Emergency Medicine Resident at The George Washington University Hospital