UMEM Educational Pearls - By Kami Windsor

Title: Fluid Resuscitation in Shock

Category: Critical Care

Keywords: circulatory dysfunction, hypotension, shock, fluid resuscitation, IV fluids (PubMed Search)

Posted: 1/1/2019 by Kami Windsor, MD
Click here to contact Kami Windsor, MD

 

The European Society of Intensive Care Medicine (ESICM) recently released a review with recommendations from an expert panel for the use of IV fluids in the resuscitation of patients with acute circulatory dysfunction, especially in settings where invasive monitoring methods and ultrasound may not be available.

 

Points made by the panel include: 

  • Circulatory dysfunction should be identified not only by HR and BP, but by other indicators of poor perfusion: altered mentation, decreased urine output, and skin abnormalities (poor skin turgor, mottling, delayed capillary refill)
  • The absence of arterial hypotension does not preclude hypovolemia
  • The lack of an increase in MAP (especially in patients with decreased vascular tone) does not exclude positive response to IVF
  • The purpose of IVF administration is to improve tissue perfusion by increasing cardiac output
  • Fluid "loading" as the rapid administration of large volumes of fluid to treat overt hypovolemia, while a fluid "challenge" is a test of fluid responsiveness
  • In elderly patients or those with arteriosclerosis or chronic arterial hypertension, a low pulse pressure (e.g. less than 40 mmHg) indicates that stroke volume is low. PP = SBP - DBP

 

Recommendations from the panel include:

  • The early measurement of lactate to incorporate in the assessment of perfusion
  • The use of crystalloids as initial resuscitation fluid (unless blood products are indicated)
  • When overt hypovolemia is unclear, the use of a fluid challenge of 150-350mL IVF within 15 minutes to help assess fluid responsiveness
  • Avoidance of using jugular venous distension alone as a guide for resuscitation
  • Avoidance of using acute urine output response alone as a guide for resuscitation, as renal response to fluids can be delayed
  • A recommendation against using CVP as a target for resuscitation; if CVP is being measured, a rapid increase with IVF should suggest poor fluid tolerance
  • Individualizing fluid resuscitation to the patient's current presentation, underlying comorbidities, and response to fluids

 

Bottom Line: Utilize all the information you have about your patient to determine whether or not they require IVF, and reevaluate their physical and biochemical (lactate) response to fluids to ensure appropriate IVF administration and avoid volume overload. 

 

 

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Title: Avoid Hyperoxia...Period!

Category: Critical Care

Keywords: hyperoxia, oxygen therapy, saturation, SpO2, critical care, mechanical ventilation (PubMed Search)

Posted: 12/4/2018 by Kami Windsor, MD
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Hyperoxia has been repeatedly demonstrated to be detrimental in a variety of patients, including those with myocardial infarction, cardiac arrest, stroke, traumatic brain injury, and requiring mechanical ventilation,1-4 and the data that hyperoxia is harmful continues to mount:

  • Systematic review and meta-analysis of 16,000 patients admitted to hospital with sepsis, trauma, MI, stroke, emergency surgery, cardiac arrest: liberal oxygenation strategy (supplemental O2 for average SpO2 96%, range 94-100%) associated with increased in-hospital and 30-day mortality compared to conservative strategy.5
  • ED patients requiring mechanical ventilation admitted to ICU: hyperoxia defined as PaO@ >120mmHg. Patients with hyperoxia in the ED had higher mortality than not only normoxic but hypoxic patients (30% v 19% v 13% respectively), and longer vent days and ICU/hospital LOS.6
  • ICU patients, majority respiratory failure, 60% requiring mechanical ventilation; hyperoxia defined as PaO2 >100mmHg. Just ONE episode of hyperoxia an independent risk factor for ICU mortality (OR 3.80, 95% CI 1.08-16.01, p=0.047).7

 

Bottom LineAvoid hyperoxia in your ED patients, both relatively stable and critically ill. Remove or turn down supplemental O2 added by well-meaning pre-hospital providers and nurses, and wean down ventilator settings (often FiO2). A target SpO2 of >92% (>88% in COPD patients) or PaO2 >55-60 is reasonable in the majority of patients.8

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A few (out of 10) tips for the care of sick patients with liver failure:

  • Use of albumin is indicated to improve outcomes in spontaneous bacterial peritonitis (SBP), large-volume paracentesis, and hepatorenal syndrome (HRS).
  • Norepinephrine remains the vasopressor of choice for nonhemorrhagic shock. Use vasopressin or terlipressin (outside the U.S.) in AKI due to HRS to maintain a target MAP and for splanchnic vasoconstriction.
  • INR does not correctly reflect coagulation performance. Platelet count and fibrinogen are the best predictors of bleeding, and thromboelastography (via TEG/ROTEM) can reduce blood products administered for hemorrhage without affecting mortality.
  • If a nasogastric tube is indicated (administration of lactulose, decompression of SBO, etcetera), presence of [non-recently banded] esophageal varices is not a contraindication.

 

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Title: Targeting Better Neurologic Outcomes by Targeting Higher MAPs Post-Cardiac Arrest

Category: Critical Care

Keywords: resuscitation, cardiac arrest, post-cardiac arrest care, blood pressure, MAP, ROSC (PubMed Search)

Posted: 11/5/2018 by Kami Windsor, MD (Updated: 11/6/2018)
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The most recent AHA guidelines for goal blood pressure after return of spontaneous circulation (ROSC) post-cardiac arrest recommend a definite mean arterial pressure (MAP) goal of > 65 mmHg.1 There is no definitive data to recommend a higher specific goal, but there is some evidence to indicate that maintaining higher MAPs may be associated with better neurologic outcomes.2

A recently published prospective, observational, multicenter cohort study looked at neurologic outcomes corresponding to different MAPs maintained in the initial 6 hours post-cardiac arrest.3

Findings: 

1. Compared to lower blood pressures (MAPs 70-90 mmHg), the cohort with MAPs > 90 mmHg had:

  • a higher rate of good neurologic function at hospital discharge (42 vs.15%, p < 0.001)
  • a higher rate of survival to 72 hours (86 vs. 74%, p=0.01) and hospital discharge (57 vs 28%, p < 0.001)

2. The association between MAP > 90 mmHg and good neurologic outcome was stronger among patients with a previous diagnosis of hypertension, and persisted regardless of initial rhythm, use of vasopressors, or whether the cardiac arrest occured in or out of hospital.

3. There was a dose-response increase in probability of good neurologic outcome among all MAP ranges above 90 mmHg, with MAP >110 mmHg having the strongest association with good neurologic outcome at hospital discharge.

Note: The results of a separate trial, the Neuroprotect post-CA trial, comparing MAPs 85-100 mmHg to the currently recommended MAP goal of >65 mmHg, are pending.4

 

Bottom Line: As per current AHA guidelines, actively avoid hypotension, and consider use of vasopressor if needed to maintain MAPs > 90 mmHg in your comatose patients post-cardiac arrest, especially those with a preexisting diagnosis of hypertension.

 

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Title: High Velocity Nasal Insufflation

Category: Critical Care

Keywords: High flow nasal cannula, acute respiratory failure, hypoxia, hypercarbia, non-invasive ventilation (PubMed Search)

Posted: 10/9/2018 by Kami Windsor, MD (Updated: 11/22/2024)
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We know that high flow nasal cannula is an option in the management of acute hypoxic respiratory failure without hypercapnea. A newer iteration of high flow, "high velocity nasal insufflation" (HVNI), may be up-and-coming.

According to its makers (Vapotherm), it is reported to work mainly by using smaller bore nasal cannulae that deliver the same flows at higher velocities, thereby more rapidly and repeatedly clearing dead space, facilitating gas exchange and potentially offering ventilatory support. 

In an industry-sponsored non-inferiority study published earlier this year:

  • 204 adult patients in 5 EDs
  • Any acute respiratory failure deemed by the treating physician to require non-invasive positive pressure ventilation (NPPV)
  • Patients randomized to either NPPV (bilevel positive airway pressure) or HVNI
  • Rate of HVNI treatment failure (26%) and intubation @ 72 hours (7%) fell within predefined noninferiority margins
  • Rates of PCO2 clearance were similar between HVNI and NPPV groups
  • The study was not powered to detect differences between different etiologies for respiratory failure
  • Authors concluded that HVNI is noninferior to NPPV for all-comer respiratory failure.

Bottom Line: 

The availability of a nasal cannula that helps with CO2 clearance would be great, and an option for patients who can't tolerate the face-mask of NPPV would be even better.

HVNI requires more investigation with better studies and external validation before it can really be considered noninferior to NPPV, but it certainly is interesting. 

 

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Title: Sodium Bicarbonate in Severe Metabolic Acidosis

Category: Critical Care

Keywords: acidosis, acidemia, sodium bicarbonate, shock (PubMed Search)

Posted: 9/11/2018 by Kami Windsor, MD
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The recently published BICAR-ICU study looked at the use of bicarb in critically ill patients with severe metabolic acidemia...

  • Multicenter, open-label, RCT, 26 French ICUs
  • Adult patients with pH < 7.2 not secondary to hypercapnia, serum bicarb < 20 not due to bicarb wasting process 
  • SOFA score > 4 or lactate > 2
  • No bicarb versus 4.2% sodium bicarb infusion titrated to pH >7.3
  • Primary outcome: Composite measure of 28-mortality and presence of any organ failure at 7 days post-randomization
  • Secondary outcomes: Need for/length of life support measures (renal-replacement, vasopressors, mechanical ventilation), SOFA score after enrollment, electrolyte effects, occurrence of ICU-acquired infections, and ICU length of stay
  • Major findings:
    • No difference in primary outcome overall
    • No difference in pressor-free days, days off RRT, dialysis dependence at ICU discharge, ICU LOS
    • Bicarb group had less need for RRT during ICU stay (35 vs 52%, p=0.0009)
    • In patients with AKI and AKIN score 2-3*, the bicarbonate group had a decrease in both 28-day mortality (46 vs 63%, p=0.0166) and presence of any organ failure at day 7 (66 vs 82%, p=0.0142)
  • Limitations:
    • Unblinded
    • A quarter of the control group actually received bicarb
    • No data regarding vent settings, ABGs to r/o ventilation effects on pH
    • 4.2% is not a standard concentration of bicarb used in the U.S.

Bottom Line

Consider administration of sodium bicarbonate for your critically ill ED patients with severe metabolic acidosis and AKI, especially if acidosis &/or renal function is not improved with usual initial measures (such as IVF, etc).

 

 

*Acute Kidney Injury Network Staging Criteria

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Title: Epinephrine in OHCA

Category: Critical Care

Keywords: Resuscitation, OHCA, prehospital medicine, cardiac arrest, epinephrine (PubMed Search)

Posted: 8/14/2018 by Kami Windsor, MD (Updated: 11/22/2024)
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The highly-awaited PARAMEDIC2 trial results are in:

  • Multicenter, double-blinded, randomized controlled trial of prehospital OHCA care
  • 1mg IV epinephrine vs saline placebo, every 3-5 minutes
  • 8014 OHCA patients over the age of 16 (excluded pregnant patients, anaphylactic and asthmatic cardiac arrests)
  • Primary outcome: 30 day survival
  • Secondary outcomes: 
    • Survival to hospital admission
    • ICU and hospital LOS
    • Survival to hospital discharge and at 3 months
    • Neurologic outcomes at hospital discharge and at 3 months, "favorable" if mRS≤3
  • Results: 
    • Higher 30 day survival in Epi group (3.2 vs 2.4%, unadj OR 1.39; 95% CI 1.06 to 1.82; P=0.02)
    • No difference in ICU or hospital LOS
    • No difference in favorable neurologic outcomes at discharge or 3 month
    • Worse neurologic outcomes in the epinephrine survivors (mRS 4 or 5 in 31% of epi group vs. 17.8% of placebo)

 

Interestingly, the authors also queried the public as to what mattered to them most: 

 

Bottom Line:

  • As has been demonstrated in previous studies, use of bolus-dose epinephrine results in increased rates of ROSC. 
  • This survival comes with the trade-off of worsened neurologic function, a condition not in a majority of patients' personal wishes.
  • Epinephrine "1mg every 3-5 minutes'" should no longer be the dogma of OHCA resuscitation.

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Title: Noninvasive Ventilation in Do-Not-Intubate Patients

Category: Critical Care

Keywords: noninvasive positive pressure ventilation, NIV, NIPPV, DNI, do-not-intubate, palliative care, end-of-life, respiratory distress (PubMed Search)

Posted: 7/17/2018 by Kami Windsor, MD
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When a do-not-intubate (DNI) hospice patient arrives in the ED with respiratory distress, consideration of non-invasive positive pressure ventilation (NIPPV) could invoke either a “What other option do I have?” or “Why torture the patient and prolong the dying process?” sentiment.

 

But what’s the data?

A recently-published meta-analysis1 found that in DNI patients receiving NIPPV, there was a 56% survival rate to hospital discharge and 32% survival to 1-year.

  • Higher survival was seen in patients with COPD and pulmonary edema as the cause of their respiratory failure, as opposed to pneumonia or malignancy.
  • In surviving patients, there was no decrease in quality of life at 3 months; quality of life was not assessed in the time before death in nonsurvivors.
  • In comfort-measures only (CMO) patients, patients receiving NIPPV had a mildly lower dyspnea score with less opiates required/administered.

 

Independent studies have demonstrated:

  • Better survival with NIPPV for DNI COPD and CHF patients2,3,4 who are awake and have a good cough.4
  • No decrease in health-related quality of life or post-ICU psychological burden (symptoms of PTSD, anxiety, or depression) in DNI survivors receiving NIPPV.3
  • 63% survival to hospital discharge & 49% survival to 90 days in DNI patients receiving NIVV, with no decrease in health-related quality of life in survivors. Survival was lower for CMO patients (14% and 0% at discharge and 90 days, respectively).5

 

Bottom Line:

  1. NIPPV can benefit DNI patients -- most identifiably those with COPD or cardiogenic pulmonary edema as the etiology for their respiratory distress.
  2. Mild benefits to dyspnea have been seen in CMO patients, without survival benefit. A trial of NIPPV therapy may be reasonable (especially in COPD or CHF) after frank discussion with the patient and his/her loved ones, with quick cessation if comfort is not achieved and/or more discomfort is caused.

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Although not specifically a part of current recommendations due to lack of data, the AHA has previously recommended shifting upward on the sternum during CPR in the pulseless pregnant patient in order to account for upward displacement of the heart by a gravid uterus. Should the same be done for our obese patients?

Lee et al. performed a retrospective study that reviewed chest CTs to determine the location on the sternum that corresponded to the optimal point of maximal left ventricular diameter (OPLV), in both obese and non-obese patients. 

They found that the OPLV was higher (more cranial) on the sternum for obese patients than for patients with normal weight, although 96% of obese patients' OPLV fell within 2cm of where the guidelines recommend standard hand placement should be, compared to a notable 52% in non-obese patients.

*as measured from the distal end of the sternum

 

Bottom Line: Radiographically, the location on the sternum that corresponds to optimal compression of the LV is more cranial in obese patients than in non-obese patients. It remains to be seen whether the recommendations for hand placement in CPR should be adjusted, but we may want to consider staying within 4cm of the bottom of the sternum in patients of normal weight. 

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Title: 2018 Surviving Sepsis Update

Category: Critical Care

Keywords: sepsis, septic shock, guidelines (PubMed Search)

Posted: 5/22/2018 by Kami Windsor, MD
Click here to contact Kami Windsor, MD

  • The Surviving Sepsis Campaign recently republished the 2018 update to their guidelines, namely, the recommendation that physicians initiate treatment measures using a "1-Hour Bundle" rather than the 3 and 6-hour bundles previously recommended:

  • Also included was the level of evidence for each bundle component. There was no additional evidence provided to support the within-one-hour recommendation. 

  • There has been no well-designed, randomized trial to demonstrate benefits to administration of the various bundle components at specific time points. There are observational studies that show benefits to early protocolized therapy, including a restrospective study by Seymour et al. that showed benefits to earlier administration of antibiotics (but notably, not IV fluid administration), primarily in patients with septic shock requiring pressors.2
  • There have been a variety of studies demonstrating harm with unecessary IV fluid administration,3-5 and inappropriate antibiotic use puts patients at risk for C.difficile colitis, drug reactions, and promotes drug-resistant organisms. Studies to date do not examine adverse events in patients initially treated for sepsis who do not end up being septic.

Take Home Points: 

  1. Early recognition of sepsis is crucial to initiating necessary therapies and improving outcomes.
  2. Patients with sepsis and septic shock benefit from early appropriate antibiotics, source control, and appropriate resuscitation.
  3. Empiric treatment of all-comers with possible sepsis with broad spectrum antibiotics and 30ml/kg of IV fluids, in order to meet a 1-hour deadline, has definite potential for harm. 

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Title: Predicting Failure of Non-invasive Ventilation and High Flow Nasal Cannula

Category: Critical Care

Keywords: acute hypoxic respiratory failure, intubation, noninvasive positive pressure ventilation, high flow nasal cannula, BiPAP, vapotherm (PubMed Search)

Posted: 4/25/2018 by Kami Windsor, MD
Click here to contact Kami Windsor, MD

ED physicians frequently utilize modailities such as noninvasive positive pressure ventilation (NIV) and high flow nasal cannula (HFNC) to support and potentially avoid intubation in patients presenting with acute hypoxic respiratory failure. Unfortunately, failure of these measures, resulting in "delayed" intubation, has been associated with increased mortality.1,2

A recent post-hoc analysis of data from a multicenter randomized controlled trial evaluated 310 patients with acute hypoxic respiratory failure managed with supplemental O2 by regular nasal cannula, HFNC, or NIV.3

The following factors were predictive of eventual intubation in the different groups: 

  • For nasal cannula patients, RR > 30 at 1 hour
  • For HFNC patients, tachycardia at 1 hour (No respiratory variables were found to predict intubation).
  • For NIV patients, tidal volume > 9ml/kg predicted body weight or PaO2:FiO2 ratio < 200 at 1 hour

Of note, 45% of the 310 patients eventually required intubation, and these patients in general had a higher initial respiratory rate and lower PaO2 at presentation, and were more likely to have bilateral infiltrates on CXR. 

Bottom Line: Reevaluate your patients frequently. If RR remains high, P:F ratio remains low, or patient respiratory effort/work of breathing is not alleviated by noninvasive measures, consider pulling the trigger on intubation earlier.

 

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Title: Avoid Hyperoxia Post-Cardiac Arrest!

Category: Critical Care

Keywords: cardiac arrest, OHCA, ROSC, targeted temperature management, oxygen, hyperoxia (PubMed Search)

Posted: 3/27/2018 by Kami Windsor, MD (Updated: 11/22/2024)
Click here to contact Kami Windsor, MD

Background:

Animal studies in post-ROSC management after cardiac arrest have repeatedly demonstrated poorer neurological outcomes with higher amounts of oxygen administration.Studies in humans have also demonstrated dose-dependent associations between hyperoxia and poorer neurologic outcomes, as well as in-hospital mortality.2,3

Recent Data

A retrospective analysis of prospectively-collected data in 187 OHCA patients undergoing postarrest care with targeted temperature management found worse neurologic outcomes in patients experiencing hyperoxia in the first 6 hours following ROSC.4

This association was dose-dependent, with worsening outcomes as with higher PaO2 levels >200.

  • Adjusted OR 1.659 [95% CI, 1.194–2.305] at 200 mmHg
  • Adjusted OR 3.969 [95% CI, 1.450–10.862] for 300 mmHg
  • Trend towards worsening at 150 mmHg that did not reach statistical significance

Bottom Line:

  • Our initial management of these patients in the ED is crucial
  • In post-cardiac arrest patients, titrate immediate FiO2 to SpO2 ≥ 94% and PaO2 75 to 150/200 mmHg to avoid hyperoxia and worsening neurologic and survival outcomes. 

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Title: Empiric Antifungal Therapy in Septic Shock

Category: Critical Care

Keywords: ICU, fungal infection, septic shock, antifungal therapy, empiric (PubMed Search)

Posted: 2/27/2018 by Kami Windsor, MD
Click here to contact Kami Windsor, MD

Which septic patients should receive empiric antifungal therapy?

Patients with fungemia only make up about 5% of patients presenting with septic shock, but invasive fungal infections are associated with increased hospital mortality (40-50%), prolonged ICU and hospital length of stay, and increased costs of care.1

The EMPIRICUS trial showed no mortality benefit to empiric antifungals for all, even patients with candidal colonization and recent exposure to antibiotics.2

Bottom Line

Therapy should always be tailored to the specific patient, but providers should strongly consider admininistering empiric echinocandin (micafungin, caspofungin) over fluconazole in patients with severe sepsis/septic shock and:

  • Immunosuppression (chronic steroids, neutropenia, organ transplant)
  • Prolonged central venous catheters
  • TPN
  • Yeast colonization
  • Severe pancreatitis
  • Recent abdominal surgeries or procedures (perforation repairs, resections, etc.) or concern for impaired gut integrity

*Especially consider addition of antifungal in patients who do not show improvements after initial management with IVF and broad spectrum antibiotics in the ED.*

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Title: Is there a benefit to steroids in septic shock?

Category: Critical Care

Keywords: sepsis, septic shock, glucocorticoids, steroids, hydrocortisone (PubMed Search)

Posted: 1/29/2018 by Kami Windsor, MD
Click here to contact Kami Windsor, MD

As hospital volumes increase and ED patient boarding becomes more commonplace, emergency physicians may find themselves managing critically ill patients beyond the initial resuscitation.

The benefit of glucocorticoids in critically ill patients with septic shock has remained a topic of controversy for decades due to conflicting studies, including the 2002 Annane trial and the 2008 CORTICUS trial, which had opposing results when it came to the mortality benefit of steroids.

The results of the eagerly-awaited ADRENAL trial, a multicenter randomized controlled trial investigating the benefit of steroids in septic shock, were released earlier this month:

  • 3658 patients from 69 different medical and surgical ICUs
  • Adults with septic shock requiring mechanical ventilation (including noninvasive) and vasopressors/inotropes for at least 4 hours
  • Continuous infusion hydrocortisone 200mg/day vs placebo for 7 days or until ICU discharge, if shorter
  • No mortality benefit at 90 days (primary outcome) or at 28 days (secondary outcome)
  • Other secondary outcomes:
    • Hydrocortisone group = Shorter ICU LOS, shorter duration of shock, shorter duration of initial mechanical ventilation, fewer # of patients receiving a blood transfusion
    • No difference in: mortality at 28 days, hospital LOS, recurrence of shock, total vent-free days, mean volume of blood transfused in patients receiving blood products, use of renal replacement therapy, development of new bacteremia/fungemia

 

Take Home Points:

1. Administration of standard daily dose hydrocortisone by infusion does not seem to affect mortality in septic shock.

2. Emergency providers should continue to consider stress-dose steroids in patients with shock and a high risk of adrenal insufficiency (e.g., chronic steroid therapy, genetic disorders, infectious adrenalitis, etc).  

 

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Title: Peri-Intubation Cardiac Arrest

Category: Critical Care

Keywords: endotracheal intubation, cardiac arrest, airway, respiratory failure (PubMed Search)

Posted: 1/2/2018 by Kami Windsor, MD (Updated: 1/4/2018)
Click here to contact Kami Windsor, MD

Although the data is limited, current published rates of in-hospital, non-operating room peri-intubation cardiac arrest (PICA) range from 2 to 6%.1,2,3

Several risk factors associated with PICA have been identified and include:

  • Preintubation hemodynamic instability (shock index ≥ 1 or systolic blood pressure < 90mmHg)1,2,3
  • Elevated Body Mass Index (and increased risk with every 10kg body weight)1
  • Use of succinylcholine as paralytic3
  • Intubation occurring within one hour of nursing shift change3

Other common findings:

  • Most PICA occurs within 10 minutes of rapid sequence induction (RSI)1,2
  • PEA is the initial recorded rhythm 80-100% of the time.1,2,3
  • Even if ROSC obtained, PICA is associated with higher rates of in-hospital mortality compared to patients requiring emergent intubation who do not experience cardiac arrest.1,2,3

 

Bottom Line:  Endotracheal intubation is one of the riskiest procedures we regularly perform as emergency physicians.

  • Resuscitate hypotensive patients prior to or concomitantly with RSI and/or have a vasopressor at the ready in patients with higher risk of cardiovascular collapse.
  • Consider use of vecuronium or rocuronium, rather than succinylcholine, in patients who require a paralytic for intubation but are at higher risk of hyperkalemia or have an unknown history. 

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Title: IVF Resuscitation in Obese Septic Patients: Not one-weight-fits-all?

Category: Critical Care

Keywords: sepsis, resuscitation, obesity, IV fluids, bolus (PubMed Search)

Posted: 12/5/2017 by Kami Windsor, MD
Click here to contact Kami Windsor, MD

Background:

We are all familiar with the Surviving Sepsis Campaign recommendation (& CMS core measure) for an initial 30ml/kg bolus of IV crystalloid within the first 3 hours for our patients with septic shock. There is minimal data, however, on how much IVF we should be giving our patients with BMIs ≥30.

 

A recent study in obese patients with septic shock retrospectively stratified the total fluids administered at 3 hours into 3 different weight categories, to categorize patients as having received 30mL per kg of ___ body weight, whether actual (ABW), adjusted (AjdBW), or ideal (IBW**).

AdjBW = (ABW – IBW) *40% + IBW

They found:

  • Most patients received fluids based on actual body weight, BUT
  • Patients at highest BMIs received ABW fluids less often
  • 30ml/kg dosing according to adjusted body weight was associated with improved mortality compared to IVF per actual or ideal body weight.

 

Bottom Line:

  • If the 30ml/kg IVF bolus seems clinically appropriate for your obese patient, consider administering according to Adjusted Body Weight first.
  • As always, reevaluate your septic shock patients frequently to determine if additional fluids are necessary, and go to vasopressors early if they are not fluid responsive.

 

**IBW calculated using Devine’s formula for men and women:

  • Males:  IBW = 50 + 2.3*(# inches over 5 feet)
  • Females: IBW = 45.5 + 2.3*(# inches over 5 feet)

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Title: Unplanned Transfers to the ICU

Category: Critical Care

Keywords: ICU, risk factors, upgrade, decompensation (PubMed Search)

Posted: 11/7/2017 by Kami Windsor, MD
Click here to contact Kami Windsor, MD

Should that patient be admitted to the floor? 

Several studies have evaluated factors associated with upgrade in admitted patients from the floor to an ICU within 24 or 48 hours. Elevated lactate, tachypnea, and "after-hours" admissions have been repeatedly identified as some of the risk factors for decompensation. 

Two recent studies tried again to identify predictors of eventual ICU requirement...

Best predictors of subsequent upgrade:

  • Hypercapnia*
  • Tachypnea (in sepsis patients)*
  • Hypoxemia (in pneumonia patients)
  • Nighttime admission
  • Initial lactate ≥ 4

The most common reasons for upgrade:

  1. Respiratory failure
  2. Hemodynamic instability

Effect on mortality

Despite a more stable initial presentation, mortality of patients who decompensated on the floor (25%) matched that of patients initially admitted to the ICU.

*One of the studies noted that although respiratory rate was demonstrated to be the most important vital sign, it was missing in 42% of the study population, while PCO2 was only obtained in 39% of patients.

Bottom Line: 

  • Make sure to physically reassess patients you've stabilized/improved in the ED with current vital signs (including an accurate respiratory rate!) before okaying their admission/transfer to the floor. 
  • If you get a blood gas, make sure to pay attention to the PCO2 and address any abnormalities appropriately.

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Title: Liver Dialysis on MARS (Molecular Adsorbent Recirculating System)

Category: Critical Care

Keywords: liver failure, dialysis, MARS, Molecular Adsorbent Recirculating System (PubMed Search)

Posted: 10/10/2017 by Kami Windsor, MD
Click here to contact Kami Windsor, MD

Molecular Adsorbent Recirculating System (MARS) is an artificial liver support system colloquially known in the medical field as "dialysis for the liver."  

  • Limited data, small studies
  • Consistently shown to improve hemodynamics, toxin clearance, and hepatic homeostasis
  • No consistent proven mortality benefit
  • Only performed by limited number of US hospitals (including the University of Maryland)
  • May depend on the acute liver failure subpopulation, but best use currently seems to be for severe acute liver failure due to a potentially reversible/recoverable cause (toxin ingestion, trauma, acute alcoholic hepatitis, etc) or as a bridge to transplant

Take-Home:

1. Consider MARS in your patient with severe acute liver failure due to potentially reversible/recoverable etiology

2. Know if and where MARS is offered near you

 

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Title: Negative-Pressure Pulmonary Edema

Category: Critical Care

Keywords: respiratory failure, pulmonary edema, airway obstruction (PubMed Search)

Posted: 9/12/2017 by Kami Windsor, MD
Click here to contact Kami Windsor, MD

Negative-pressure pulmonary edema (NPPE) is a well-documented entity that occurs after a patient makes strong inspiratory effort against a blocked airway. The negative pressure causes hydrostatic edema that can be life-threatening if not recognized, but if treated quickly and appropriately, usually resolves after 24-48 hours. These patients may have any type of airway obstruction, whether due to edema secondary to infection or allergy, laryngospasm, or traumatic disruption of the airway, such as in attempted hangings.

Management: 

1.     Alleviate or bypass the airway obstruction.

·      Usually via intubation; may require a surgical airway

·      If obstruction in an intubated patient is due to biting on tube or dyssynchrony, add bite-block (if not already in place), sedation, and even paralysis if needed.

2.     Provide positive pressure ventilation and oxygen supplementation.

3.     Use low tidal volume ventilation.

4.     In severe hypoxemia without shock, add a diuretic agent and consider additional measures such as proning and even ECMO if the hypoxemia is refractory to standard therapy.  

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Background: Sedation and analgesia are key components for mechanically ventilated patients. While significant data exists regarding how to manage sedation and analgesia in the ICU setting, very little data exists on management in the ED.

Data: A prospective, single-center, observational study of mechanically-ventilated adult patients used linear regression to identify ED sedation practices and outcomes, with a focus on sedation characteristics using the Richmond Agitation-Sedation Scale (RASS).

Findings:

  • 15% of intubated patients had no sedation or analgesia ordered
  • 64% of intubated patients were documented as deeply-sedated (RASS -3 to -5)
  • Deep sedation was not only associated with more ventilator days, but also increased mortality, with an adjusted OR of 0.77 (95% CI 0.54-0.94) favoring patients with lighter sedation.


Bottom line:  Avoid early deep sedation in your intubated patients as this may be directly associated with increased mortality. Instead, a goal RASS of 0 to -2 should be appropriate for most non-paralyzed, mechanically-ventilated ED patients, extrapoloating from ICU guidelines.

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