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Title: Fall in the Elderly (Submitted by Heidi M. Teague, MD)

Category: Geriatrics

Keywords: geriatric, trauma, imaging (PubMed Search)

Posted: 4/3/2017 by Danya Khoujah, MBBS

·       In the elderly, falling is the most common mechanism of injury
·       Unavoidable Risk factors: age 85 or older, male, Caucasian, history of falls
·       Other factors: alcohol consumption, polypharmacy
·       Mechanisms of fall:  slipping, tripping, stumbling
·       Physical exam to include: gait, balance, proprioception, vision, strength and cognitive function testing
·       Must consider neglect/abuse, affects 10% of seniors per year
·       Evaluate for anticoagulant use due to increased risk of intracranial injury
·       Use advanced imaging to identify occult hip fractures when clinically suspected and plain radiographs are negative

 

Show References

Abraham, MK, Cimino-Fiallos, NE.  Falls in the Elderly: Causes, Injuries, and Management. Medscape February 1, 2017.

http://reference.medscape.com/features/slideshow/falls-in-the-elderly



Title: On your radar: methadone-linezolid drug-drug interaction

Category: Pharmacology & Therapeutics

Keywords: methadone, linezolid, serotonin syndrome, drug interaction (PubMed Search)

Posted: 4/1/2017 by Michelle Hines, PharmD (Updated: 4/3/2017)

Linezolid is a weak, nonselective monoamine oxidase inhibitor (MAOI). A recent FDA Drug Safety Communication released in March 2016 noted reports of serotonin syndrome associated with certain opioids, particularly fentanyl and methadone. Development of serotonin syndrome after concomitant administration of linezolid with other serotonergic agents has been reported. Due to a potential risk of serotonin syndrome, a patient on chronic methadone should not be started on concomitant linezolid unless they will be monitored.

Show References

  1. FDA Drug Safety Communication from 3/22/2016: https://www.fda.gov/downloads/Drugs/DrugSafety/UCM491302.pdf
  2. Product Information: DOLOPHINE(R) oral tablets, methadone HCl oral tablets. West-Ward Pharmaceuticals Corp. (per FDA), Eatontown, NJ, 2016.
  3. Product Information: ZYVOX(R) intravenous injection, oral tablets, oral suspension, linezolid intravenous injection, oral tablets, oral suspension. Pharmacia & Upjohn Co (per FDA), New York, NY, 2013.

Follow me on Twitter @mEDPharmD



Title: Pediatric Sepsis (submitted by Lauren Grandpre, MD)

Category: Pediatrics

Keywords: pediatric, sepsis, infection, infants, children (PubMed Search)

Posted: 3/31/2017 by Mimi Lu, MD

Sepsis remains the most common cause of death in infants and children worldwide, with pneumonia being the most common cause of pediatric sepsis overall.

Strikingly, however, the mortality rate in pediatric sepsis is significant lower in children (10-20%) as compared to adults (35-50%).

The management of pediatric sepsis has been largely influenced by and extrapolated from studies performed in adults, in part due to difficulties performing clinical trial data in children with critical illness, including sepsis.

A major difference in management of children vs. adults with refractory septic shock with or without refractory hypoxemia from severe respiratory infection is the dramatic survival advantage of children when ECMO rescue therapy is used as compared to adults.

Bottom line: Consider ECMO for refractory pediatric septic shock with respiratory failure – in kids, survival is improved dramatically – consider it early!

Show Additional Information

For respiratory distress and hypoxia: Infants have a lower FRC and can desaturate very quickly!

Supplemental O2 should be delivered via face mask or nasal cannula or other devices such as high flow nasal cannula or nasopharyngeal CPAP, even if O2 saturation levels appear normal with peripheral monitoring devices

For improved circulation: utilize peripheral IO early

Peripheral IV or IO access can be used for fluid resuscitation, inotrope infusion, and antibiotic delivery when central access is not readily available or obtainable

Initial therapeutic resuscitative end points: hypotension and poor capillary refill may portend imminent cardiovascular collapse!

  • Capillary refill of < or = 2s
  • Normalization of heart rate for age
  • Normalization of blood pressure for age
  • Lack of difference between central and peripheral pulses
  • Warm extremities
  • Urine output >1mL/kg/hr
  • Normal level of consciousness

Antibiotics and source control: Early and aggressive source control is key, just as in adults!

  • In up to 75% of pediatric sepsis cases, the underlying pathogen(s) remain unknown,
  • A child’s immune system is incompletely formed, and they are markedly more susceptible to viruses and encapsulated bacteria
  • Empiric antibiotics should be administered within 1 hour
  • Blood cultures prior to antibiotics is preferred, but should not delay starting antibiotics
  • Tailor antimicrobials to epidemic and endemic ecologies and consider resistant organisms
  • Clindamycin and anti-toxin therapies for toxic shock syndromes with refractory hypotension
  • C. diff. colitis should be treated with enteral antibiotics if possible, with vancomycin preferred in severe cases

Fluid resuscitation: Support the pump, and fill, but don’t overload the tank!

  • Bolus 20 mL/kg fluid (isotonic crystalloid) IV/IO over 5-20min or faster if needed
  • Repeat 20 mL/kg bolus of fluid (up to 60 mL/kg) until clinical symptoms improve or patient develops respiratory distress/rales/ hepatomegaly
  • Titrate to reversing hypotension, increasing urine output, and attaining normal capillary refill, peripheral pulses, and level of consciousness
  • If hepatomegaly or rales are present, consider early inotropic support and carefully titrated fluids
  • Use diuretics to reverse fluid overload when shock has resolved, and if unsuccessful then CVVH or intermittent dialysis to prevent >10% total body weight fluid overload
  • In non-hypotensive children with severe hemolytic anemia (i.e. severe malaria or sickle cell crisis) blood transfusion is considered superior to crystalloids
  • Consider adrenal insufficiency in refractory shock and give hydrocortisone accordingly

Inotropes and vasopressors: not just Levo for all!

  • Normotensive shock (impaired perfusion but normal blood pressure): Dopamine 2-20 mcg/kg/min IV/IO, titrate to desired effect; if continued poor perfusion, consider dobutamine infusion 2-20 mcg/kg/min IV/IO, titrate to desired effect (may cause hypotension, tachycardia)
  • Warm shock (warm extremities, flash capillary refill): Norepinephrine 0.1-2 mcg/kg/min IV/IO infusion, titrate to desired effect
  • Cold shock (cool extremities, delayed capillary refill): Epinephrine 0.1-1 mcg/kg/min IV/IO infusion, titrate to desired effect

Extracorporeal Membrane Oxygenation (ECMO)

Consider ECMO for refractory pediatric septic shock with respiratory failure – in kids, survival is improved dramatically – consider it early!

Blood products

  • In hemodynamically unstable children in shock on pressors, hgb levels of ≥10 g/dL are targeted
  • In stable critically ill children, a lower hgb target of ≥7.0 g/dL is recommended
  • Similar platelet transfusion targets in children as in adults
  • Consider plasma therapies in children to correct sepsis-induced thrombotic disorders
  • IV immunoglobulin may also be considered

Mechanical ventilation

  • If mechanical ventilation is required, then cardiovascular instability during intubation may be less likely after appropriate cardiovascular resuscitation
  • Use lung-protective strategies during mechanical ventilation
  • Sedation/analgesia is recommended in critically ill mechanically ventilated kids with sepsis

Glycemic control

  • Watch for hypoglycemia (neonates < 45 mg/dL, infants/children < 60 mg/dL)
  • Control hyperglycemia using similar targets as in adults < or = 180 mg/dL

Show References

Randolph AG & McCulloh RJ. Pediatric sepsis: important considerations for diagnosing and managing severe infections in infants, children, and adolescents. Virulence. 2014: 1;5(1):179-89. doi: 10.4161/viru.27045.

Wheeler DS, Wong HR, Zingarelli B. Pediatric Sepsis - Part I: "Children are not small adults!" Open Inflamm J. 2011: 7;4:4-15. doi: 10.2174/1875041901104010004.



Title: Pediatric poisoning trends

Category: Toxicology

Keywords: Pediatric poisoning, household , fatalities (PubMed Search)

Posted: 3/30/2017 by Kathy Prybys, MD

Children less than 5 years of age account for the majority of poisoning exposures in the United States. As expected, accessible household items are the most frequently reported exposures and include cosmetics and personal care products, household cleaning substances, medications, and foreign bodies. Opioids are responsible for the highest incidence of hospitalizations followed by benzodiazepines, sulfonylureas, and cardiovascular drugs (beta & calcium channel blockers, and centrally acting antiadrenergic agents).  Rise in buprenorphine use has led to significant increases in pediatric exposures. The most common sources of prescription medications were pills found on the ground, in a purse or bag, night stand, or pillbox. The 2015 American Association of Poison Centers Annual report lists 28 fatalities in children less than 5 year of age. Fatalities occurred from exposures to the following: narcotics (9), disc and button batteries (5), carbon monoxide (4), and other substances (10). 

Highlighted AAPC cases include:

  •  20 month old with ingestion of 20 mm Lithuim disc battery with several previous ED visits for abdominal pain who developed an aorto-esophageal fistula 
  • 13 month old with ingestion of unknown amount of salicylate pills 4 hours earlier with nausea and vomiting
  • 2 year old with ingestion of 5 tablets of 30mg Oxycodone ER seen in ED and discharged 7 hours later. EMS called next morning found patient unresponsive and apneic
  • 11 month old with ingestion of 1 unknown strength methadone pill found unresponsive and apneic at home

Poison prevention education of patients prescribed opioids or other highly toxic "one pill killers"  who have young children in their household is recommended and could be potentially life saving.

 

 

 

 

 

 

 

 

Show References

2015 Annual Report of the American Association of Poison Centers' National Poison Data System: 33rd Annual Report.  Mowrey JB, et al. Clinical Toxicology, 54:10.924-1109.

Emergency Hospitalizations for Unsupervised Prescription Medication Ingestions by Young Children, Lovegrove MC, et al. Pediatrics. 2014,134 (4) e1009-e1016 .

The Underrecognized Toll of Prescription Opioid Abuse on Young Children. Bailey JE, et al. Ann of Emerg Med. April 2009:53(4): 419-24. doi:10.1016/j.annemergmed.2008.07.015.Epub 2008 Sep 6.



Title: Falls in the elderly

Category: International EM

Keywords: Falls, elderly (PubMed Search)

Posted: 3/29/2017 by Jon Mark Hirshon, MPH, MD, PhD (Updated: 7/21/2026)

·       Falls are the second leading cause of accidental or unintentional injury deaths worldwide.

·       Each year an estimated 424 000 individuals die from falls globally of which over 80% are in low- and middle-income countries.

·       Adults older than 65 suffer the greatest number of fatal falls.

·       37.3 million falls that are severe enough to require medical attention, occur each year.

·       Prevention strategies should emphasize education, training, creating safer environments, prioritizing fall-related research and establishing effective policies to reduce risk.

Show References

http://www.who.int/mediacentre/factsheets/fs344/en/



Title: Ketamine is Not Without Risk

Category: Critical Care

Posted: 3/28/2017 by Mike Winters, MBA, MD (Updated: 7/21/2026)

DSI, Ketamine, and Apnea

  • In recent years, delayed sequence intubation (DSI) with ketamine has been used in select patients to maximize preoxygenation and dinitrogenation. 
  • Importantly, DSI is not well studied. In the only prospective trial of DSI, patients received approximately 1.4 mg/kg of ketamine.
  • Driver, et al. report the abrupt onset of apnea in a patient who received a much lower dose of ketamine (25 mg) for DSI.
  • Take Home Point: If DSI is a part of your preoxygenation armamentarium, apnea can occur even at low doses of ketamine.  Stand at the patient's bedside and be ready to immediately intubate the patient.

Show References

Driver BE, Reardon RF. Apnea after low-dose ketamine sedation during attempted delayed sequence intubation. Ann Emerg Med 2017; 69:34-35.



Title: Responsibilities of the local team physician

Category: Orthopedics

Keywords: team doctor, sports medicine (PubMed Search)

Posted: 3/25/2017 by Brian Corwell, MD (Updated: 7/21/2026)

Question

Physicians are often called upon to serve as a team physician for a local high school in an official or unofficial capacity.

To aid in preparedness for sport-related emergencies, multiple national organizations have defined institutional best practices.

Knowledge of the following 3 best practice recommendations is important before taking on the role of “Doc covering the game”

     1)The written Emergency Action Plan (EAP) – details the standard of emergency care at the particular venue.

     2)The availability of life saving equipment: AED – where is it, charged and working?

     3)Are the coaches trained in use of the AED and CPR. You can’t be everywhere and often multiple sporting events occur on campus simultaneously. It’s imperative that your first responder (coach or athletic trainer) can perform these tasks until you are able to respond

Please investigate these best practice recommendations before agreeing to serve as the physician for the local high school.

Show Answer



Title: Blistering Distal Dactylics (submitted by Nicole Cimino-Fiallos, MD)

Category: Pediatrics

Keywords: rash, fingertip, bulla, nail disorder (PubMed Search)

Posted: 3/24/2017 by Mimi Lu, MD

Who- Mostly seen in children, but sometimes in immunocompromised adults
What- Peri-ungal infection of the fingerpad with pus-filled blister with erythematous base
Cause- May result from thumb or finger sucking. Staph and strep are the most common bugs, but it can be caused by MRSA.
DDx- herpetic whitlow, paronychia/felon, friction blister, insect bite
Treatment-
1. De-roof the blister
2. Send drainage for culture
3. Treat for staph and strep- no indication to treat for MRSA initially unless strong suspicion
4. 10 day course of antibiotics recommended
For additional information and image: http://www.medscape.com/viewarticle/718695_3

Show References

1) Fretzayas A1, Moustaki M, Tsagris V, Brozou T, Nicolaidou P. MRSA blistering distal dactylitis and review of reported cases. Pediatr Dermatol. 2011 Jul-Aug;28(4):433-5. PMID: 21438916.

2) Cohen R, Levy C, Cohen J, Corrard F, Deberdt P, Béchet S, Bonacorsi S, Bidet P. Diagnostic of group A streptococcal blistering distal dactylitis. Arch Pediatr. 2014 Nov;21

 



Title: How often do we encounter the signs and symptoms of clonidine overdose?

Category: Toxicology

Keywords: adult clonidine overdose (PubMed Search)

Posted: 3/24/2017 by Hong Kim, MD (Updated: 7/21/2026)

Clinical signs and symptoms of clonidine overdose include CNS depression, bradycardia, and miosis. Other effects include early hypertension, followed by hypotension and respiratory depression, especially in children.

 

Although clonidine overdose in children is well described, frequency of clinical signs/symptoms in adults is not well characterized.

 

Recently, a retrospective study was performed in a hospital in Australia looking at clonidine overdose in adults.  

 

Among isolated clonidine overdose, patients experienced:

  • GCS < 15: 55%
  • GSS < 9: 5%
  • Miosis: 25%
  • Bradycardia (HR< 60): 68%
  • Median HR: 48 (IQR: 40-62)
  • Hypotension (SBP < 90 mmHg): 25%
  • Median LOS: 21 hr (IQR: 11 – 27 hr)
  • Intensive care: 23%
  • No deaths

Bottom line:

  1. The most common symtom of clonidicine overdose was bradycardia
  2. Clonidine overdose results in non-life threatening but prolonged clinical effect in adult.

Show References

Isbister GK et al. Adult clonidine overdose: prolonged bradycarida and central nervous system depression, but not severe toxicity. Clin Toxicol 2017;55:187-192.



Title: Stroke and Pregnancy: What's Different?

Category: Neurology

Keywords: CT, MRI, tPA, peripartum, PRES (PubMed Search)

Posted: 3/22/2017 by Danya Khoujah, MBBS (Updated: 7/21/2026)

  • The incidence of stroke (both ischemic and hemorrhagic) in pregnant and peripartum women is three times age-matched controls. This increased risk is mostly in the 3rd trimester and up to 16 weeks postpartum. 
  • Consider other causes of stroke:  posterior reversible encephalopathy syndrome (PRES), reversible cerebral vasoconstriction syndrome, cerebral venous sinus thrombosis and cardioembolic stroke from peripartum cardiomyopathy.
  • CTs carry some risk due to the ionizing radiation, but with abdominal and pelvic shielding the exposure to the fetus is very low. MRIs do not carry that risk, but Gadolinium is absolutely contraindicated in pregnancy as it deposits in fetal tissue. 
  • Pregnancy is a relative (not absolute) contraindication for tPA.

Show References

Majerisk JJ. Inherited and Uncommon Causes of Stroke. Continuum 2017;23(1):211–237.



Title: Lung Protective Ventilation in the Emergency Deparment

Category: Critical Care

Keywords: lung protective ventilation, ARDS (PubMed Search)

Posted: 3/21/2017 by Rory Spiegel, MD (Updated: 7/21/2026)

While lung protective ventilatory strategies have long been accepted as vital to the management of patients undergoing mechanical ventilation, the translation of such practices to the Emergency Department is still limited and inconsistent.

Fuller et al employed a protocol ensuring lung-protective tidal volumes, appropriate setting of positive end-expiratory pressure, rapid weaning of FiO2, and elevating the head-of-bed. The authors found the number of patients who had lung protective strategies employed in the Emergency Department increased from 46.0% to 76.7%. This increase in protective strategies was associated with a 7.1% decrease in the rate of pulmonary complications (ARDS and VACs), 14.5% vs 7.4%, and a 14.3% decrease in in-hospital mortality, 34.1% vs 19.6%.

Show References

Fuller BM, Ferguson IT, Mohr NM, et al. Lung-Protective Ventilation Initiated in the Emergency Department (LOV-ED): A Quasi-Experimental, Before-After Trial. Ann Emerg Med. 2017;



Title: Lung Protective Ventilation in the Emergency Deparment

Category: Critical Care

Keywords: lung protective ventilation, ARDS (PubMed Search)

Posted: 3/21/2017 by Rory Spiegel, MD

While lung protective ventilatory strategies have long been accepted as vital to the management of patients undergoing mechanical ventilation, the translation of such practices to the Emergency Department is still limited and inconsistent.

Fuller et al employed a protocol ensuring lung-protective tidal volumes, appropriate setting of positive end-expiratory pressure, rapid weaning of FiO2, and elevating the head-of-bed. The authors found that the number of patients who had lung protective strategies employed in the Emergency Department increased from 46.0% to 76.7%. This increase in protective strategies was associated with a 7.1% decrease in the rate of pulmonary complications (ARDS and VACs), 14.5% vs 7.4%, and a 14.3% decrease in in-hospital mortality, 34.1% vs 19.6%.

Show References

Fuller BM, Ferguson IT, Mohr NM, et al. Lung-Protective Ventilation Initiated in the Emergency Department (LOV-ED): A Quasi-Experimental, Before-After Trial. Ann Emerg Med. 2017;



Title: Acute Phenytoin Toxicity

Category: Toxicology

Keywords: Dilantin, Ataxia (PubMed Search)

Posted: 3/16/2017 by Kathy Prybys, MD

Phenytoin is a first line anticonvulsant agent for most seizure disorders with the exception of absence and toxin-induced seizures. It has erratic gastrointestinal absorption with peak serum levels occurring anywhere from 3-12 hours following a single oral dose. 90% of circulating phenytoin is bound to albumin but only the unbound free fraction is active to cross cell membranes and exert pharmacological effect. Measured serum phenytoin levels reflect the total serum concentration of both the free and protein bound portions. Therapeutic range is between 10-20 mg/L. Free phenytoin levels are not often measured but are normally between 1-2 mg/L. Individuals with decreased protein binding (elderly, malnourished, hypoalbuminemia, uremia, and competing drugs) may have clincial toxicity despite a normal total phenytoin level. Toxicity consists of predominantly ocular and neurologic manifestations involving the vestibular and cerebellar systems:

Plasma level, µg/mL    Clinical manifestations
<10     Usually none
10-20     Occasional mild nystagmus
20-30     Nystagmus
30-40     Ataxia, slurred speech, extrapyramindal effects 
40-50     Lethargy, confusion
>50     Coma, rare seizures

Treatment of overdose is primarily supportive with serial drug level testing and neurologic exams. There is no evidence that gastrointestinal decontamination improves outcome. Routine cardiac monitoring is not necessary for overdose following oral ingestions. Cardiac toxicity is rarely seen and only with parenteral administration. 

Show References

Phenytoin posisoning. Craig S. Neurocrit Care. 2005;3(2): 161-70. 

Severe oral phenytoin overdose does not cause cardiovascular morbidity. Wyte CD, et al. Annals of EM. 1997; 20(5). 508-512.

Cardiac Monitoring after phenytoin overdose. Evers M, et al. Heart & Lung. 1997; 26:325-328.



Title: New Antibiotics Desperately Needed

Category: International EM

Keywords: Antibiotic resistance, bacterial pathogens (PubMed Search)

Posted: 3/15/2017 by Jon Mark Hirshon, MPH, MD, PhD

The World Health Organization (WHO) recently published their first ever list of antibiotic-resistant "priority pathogens".  These 12 families of bacterial pathogens have the potential to be a significant threat to human health.

 

These bacteria are divided in critical, high and medium priority pathogens. 

 

The critical pathogens requiring R & D for new antibiotics are:

 

1.     Acinetobacter baumannii, carbapenem-resistant

2.     Pseudomonas aeruginosa, carbapenem-resistant

3.     Enterobacteriaceae, carbapenem-resistant, ESBL-producing

Show References

http://www.who.int/mediacentre/news/releases/2017/bacteria-antibiotics-needed/en/



Title: Groin Pain in Athletes

Category: Orthopedics

Keywords: stress fracture, runner (PubMed Search)

Posted: 3/11/2017 by Brian Corwell, MD

22yo college track athlete presents with 3 weeks of gradual onset groin and thigh pain, worse with running, better with rest.

Stress fractures are a common cause of groin pain in athletes, particularly in long distance runners

Fractures occur in the pubic rami and femoral neck 

Ask about a sudden change in training regimens

PE: check for tenderness to deep palpation over the pubic ramus. Ask athlete to stand and support full weight on affected leg or perform one legged hop on affected side. Pain out of proportion to physical examination findings. 

Imaging: XR usually negative. Bone scans can be positive as early as 4 to 8 days after symptom onset. MRI used to diagnose and rule out other causes of groin pain.

Treatment: Rest for 4 to 6 weeks. Consider making patient non weight bearing if walking causes pain especially with femoral neck fractures on the superior side. Inferior side neck fractures may benefit from prophylactic fixation.

 

Show References

Groin Injuries (Athletic Pubalgia) and return to play. Elattar et al., Sports Health Aug 2016.



Title: IV Fluids for Headache?

Category: Neurology

Keywords: headache, migraine, intravenous fluids, IVF (PubMed Search)

Posted: 3/8/2017 by WanTsu Wendy Chang, MD

 
IV Fluids for Headache?
  • Headache is the 4th most common ED visit in the US.
  • Clinical experience suggests that IV fluids (IVF) are commonly used as adjunctive treatment for headaches, however, the efficacy is unknown.
  • A retrospective study using the National Hospital Ambulatory Medical Care Survey (NHAMCS) found that ED length of stay was significantly greater in patients who received IVF than in those who did not (202 min vs. 131 min, p<0.001) even after adjusting for initial pain score, sex, age, and mode of arrival. 
  • A post-hoc analysis of data collected from 4 ED-based migraine trials found that IVF was not associated with improvement of pain score or sustained headache freedom.
  • There is no current evidence to suggest a direct analgesic effect of IVF in the treatment of headaches.

 

Show References

  • Jones CW, et al. Epidemiology of intravenous fluid use for headache treatment: Findings from the National Hospital Ambulatory Medical Care Survey. Am J Emerg Med. 2017. [Epub ahead of print]
  • Balbin JEB, et al. Intravenous fluids for migraine: a post hoc analysis of clinical trial data. Am J Emerg Med. 2016;34:713-6.

Follow me on Twitter @EM_NCC



Title: Preoxygenation in the Critically Ill

Category: Critical Care

Posted: 3/7/2017 by Mike Winters, MBA, MD (Updated: 7/21/2026)

Preoxygenation in Critically Ill Patients

  • Achieving adequate preoxygenation and denitrogenation prior to intubating critically ill patients can be challenging.
  • Critically ill patients have physiologic alterations (i.e., derangements in oxygen consumption, anemia, reduced cardiac output, air space disease) that can markedly reduce safe apnea time.
  • For patients with significant air space disease and shunt physiology, noninvasive ventilation (NIV) can decrease shunt fraction, increase functional residual capacity, improve PaO2, and lengthen safe apnea time.
  • Importantly, NIV should be used for at least 3 minutes to achieve improvements in alveolar recruitment.
  • It is also important to remove NIV just prior to larygnoscopy, as alveoli will begin to derecruit when NIV is removed.

Show References

Mosier JM, Hypes CD, Sackles JC. Understanding preoxygenation and apneic oxygenation during intubation in the critically ill. Intensive Care Med. 2017; 43:226-8.



Title: Inappropriate Medications - Submitted by Jill Logan, PharmD, BCPS

Category: Geriatrics

Keywords: Beers list, iatrogenic, medications, pharmacology (PubMed Search)

Posted: 3/5/2017 by Danya Khoujah, MBBS

The Beers' Criteria lists 34 classes of medications that may be potentially inappropriate for geriatric patients due to a high risk of complications including increased risk for falls. When prescribing medications from the emergency department in geriatric patients, try to avoid these categories if other options are available.

http://www.americangeriatrics.org/files/documents/beers/BeersCriteriaPublicTranslation.pdf

Show References

The AGS Foundation for Health in Aging. Identifying Medications that Older Adults Should Avoid or Use with Caution: the 2012 American Geriatrics Society Updated Beers Criteria. 2012. Retrieved on March 5th, 2017 from: http://www.americangeriatrics.org/files/documents/beers/BeersCriteriaPublicTranslation.pdf



Title: Naproxen plus adjunct diazepam or placebo for low back pain

Category: Pharmacology & Therapeutics

Keywords: NSAID, diazepam, back pain (PubMed Search)

Posted: 3/4/2017 by Michelle Hines, PharmD (Updated: 7/21/2026)

The addition of diazepam to naproxen for patients with acute, nontraumatic, nonradicular lower back pain did not improve pain or functional outcomes at 1 week or 3 months after ED discharge compared to placebo.

Show Additional Information

Study design: single-center, prospective, randomized, double-blind, placebo-controlled trial

Patients:

  • Adults age 21 to 69 years who preseted to the ED for management of nontraumatic, nonradicular low back pain <2 weeks in duration with score >5 on Roland-Morris Disability Questionnaire (RMDQ) who were discharged home from the ED
  • Exclusion criteria: radicular back pain, nonmusculoskeletal etiology of pain, direct back trauma within past 1 month, pregnant/breast feeding, chronic pain syndrome

Treatment groups:

  • Control: naproxen 500 mg PO twice daily + placebo 1-2 tablets PO every 12 hours PRN pain
  • Intervention: naproxen 500 mg PO twice daily + diazepam 5 to 10 mg PO every 12 hours PRN pain

Outcomes:

  • Primary: RMDQ score 1 week after ED discharge
  • Secondary: pain intensity 1 week and 3 months after ED discharge

Results:

  • Of 545 patients assessed for enrollment, data from 57 in the diazepam group and 55 in the placebo group were included in the primary outcome analysis
  • No difference in mean improvement in RMDQ score between the naproxen + placebo (11; 95% CI 8 to 13) and naproxen + diazepam (11; 95% CI 9 to 13) groups at 1 week
  • No difference in incidence of moderate or severe low back pain between the naproxen + placebo (22%; 95% CI 13% to 35%) or naproxen + diazepam (32%; 95% CI 21% to 45%) groups at 1 week or 3 months (naproxen + placebo, 9%; 95% CI 4% to 21%) (naproxen + diazepam, 12%; 95% CI 5% to 24%)
  • No difference in the incidence of adverse effects between groups

Conclusions:

  • The addition of diazepam to naproxen for patients with acute, nontraumatic, nonradicular lower back pain did not improve pain or functional outcomes at 1 week or 3 months after ED discharge compared to placebo.
  • This study does not support adding diazepam to an NSAID to outpatient therapy for acute, nontraumatic, nonradicular low back pain.

Show References

Citation: Friedman BW, Irizarry E, Solorzano C, et al. Diazepam is no better than placebo when added to naproxen for acute low back pain. Ann Emerg Med 2017. PMID 28187918

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Title: Drug induced Excited Delirium

Category: Toxicology

Keywords: EDS, Excited Delirium (PubMed Search)

Posted: 3/2/2017 by Kathy Prybys, MD

Excited delirium syndrome (EDS) is a life-threatening condition caused by a variety of factors including drug intoxication.  EDS is defined as altered mental status, hyperadrenergic state, and combativeness or aggressiveness. It is characterized by tolerance to significant pain, tachypnea, diaphoresis, severe agitation, hyperthermia, non-compliance or poor awareness to direction from police or medical personnel, lack of fatigue, superhuman strength, and inappropriate clothing for the current environment. These patients are at high risk for sudden death. Toxins associated with this syndrome include:

  • Lysergic acid diethylamide (LSD)
  • Phencyclidine (PCP)
  • 3,4-methylenedioxymethamphetamine (Ecstasy)
  • Cocaine
  • Methamphetamine
  • Synthetic cathinones ("Bath salts") = Mephedrone, Methylone,  Methylenedioxypyrovalerone (MDPV), designer drugs similar to amphetamine.
  • Synthetic cannbinoids

Ketamine at 4mg/kg dose can be given by intramuscular route and has been demonstrated to be safe and effective treatment for EDS.

Show References

Top 10 Facts You Need to Know About Synthetic Cannabinoids: Not So Nice Spice Kemp, Ann M. et al. The American Journal of Medicine , Volume 129 , Issue 3 , 240 - 244.

Synthetic cannabinoid drug use as a cause or contributory cause of death. Labay, LM. et al. Forensic Science International , Volume 260 , 31 - 39.

Sudden Death Due To Acute Cocaine Toxicity—Excited Delirium in a Body Packer. Sheilds, LB, Rolf CM, et al. J Forensic Sci, 2015. 60: 1647–1651.

Excited Delirium and Sudden Death: A Syndromal Disorder at the Extreme End of the Neuropsychiatric Continuum.  Mash, DC.Frontiers in Physiology. 2016; 7:435. 

Prehospital Ketamine is a Safe and Effective Treatment for Excited Delirium in a Community Hospital Based EMS System, Scaggs, TR, Glass, DM, et al. Prehospital and Disaster Medicine. 2016 31(5), 563–569. 



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