Effect of Continuous Infusion of Hypertonic Saline vs Standard Care on 6-Mont...Khaled Ali Ghanayem
Effect of Continuous Infusion of Hypertonic Saline vs Standard Care on 6-Month Neurological Outcomes in Patients With Traumatic Brain Injury The COBI Randomized Clinical Trial - Journal club.
JAMA. 2021;325(20):2056-2066. doi:10.1001/jama.2021.5561
Effect of Continuous Infusion of Hypertonic Saline vs Standard Care on 6-Mont...Khaled Ali Ghanayem
Effect of Continuous Infusion of Hypertonic Saline vs Standard Care on 6-Month Neurological Outcomes in Patients With Traumatic Brain Injury The COBI Randomized Clinical Trial - Journal club.
JAMA. 2021;325(20):2056-2066. doi:10.1001/jama.2021.5561
Review of 2 metaanalyses of RCTs on the effects of statins in the perioperative period. Watch my YouTube video describing these slides: http://youtu.be/wHYlf26AH00
Patients admitted to the ICU after cardiac arrest have, by definition, achieved ROSC. In such patients the major issues remain those of ongoing support hemodynamic and cardiorespiratory support, cerebral protection, aetiological diagnosis, and rapid intervention to deal with the underlying trigger (coronary angiography and stenting of coronary artery disease or CT pulmonary angiography and anticoagulation/thrombolysis for PE). Once the aetiological diagnosis has been made and its cases addresses and cardiovascular stability has been achieved, the priority of care is directed toward cerebral protection. Previous randomized controlled trials had suggested that hypothermia would deliver superior neurological outcomes compared to usual care. However, methodological concerns led to a further large trial of strict normothermia (TTM-1) which found strict normothermia to be equivalent to hypothermia in terms of neurological outcomes. Such findings have led to the design and randomization of patients with out of hospital cardiac arrest (OOHCA) to normothermia vs. avoidance of fever (TTM-2). At the same time preliminary work has demonstrated the potential of hypercapnia to act as a cerebral protector in patients with OOHCA. His has now led to a large trail called TAME, which currently also recruiting patients worldwide and in ANZ. These two trials will provide important information on the outcome of OOHCA patients and may identify new ways of achieving cerebral protection in this setting.
Implementing American Heart Association Practice Standards for Inpatient ECG ...Allina Health
Implementing American Heart Association Practice Standards for Inpatient ECG Monitoring: An Interventional Study at Abbott Northwestern Hospital presented by Kristin Sandau, PhD, RN
Review of 2 metaanalyses of RCTs on the effects of statins in the perioperative period. Watch my YouTube video describing these slides: http://youtu.be/wHYlf26AH00
Patients admitted to the ICU after cardiac arrest have, by definition, achieved ROSC. In such patients the major issues remain those of ongoing support hemodynamic and cardiorespiratory support, cerebral protection, aetiological diagnosis, and rapid intervention to deal with the underlying trigger (coronary angiography and stenting of coronary artery disease or CT pulmonary angiography and anticoagulation/thrombolysis for PE). Once the aetiological diagnosis has been made and its cases addresses and cardiovascular stability has been achieved, the priority of care is directed toward cerebral protection. Previous randomized controlled trials had suggested that hypothermia would deliver superior neurological outcomes compared to usual care. However, methodological concerns led to a further large trial of strict normothermia (TTM-1) which found strict normothermia to be equivalent to hypothermia in terms of neurological outcomes. Such findings have led to the design and randomization of patients with out of hospital cardiac arrest (OOHCA) to normothermia vs. avoidance of fever (TTM-2). At the same time preliminary work has demonstrated the potential of hypercapnia to act as a cerebral protector in patients with OOHCA. His has now led to a large trail called TAME, which currently also recruiting patients worldwide and in ANZ. These two trials will provide important information on the outcome of OOHCA patients and may identify new ways of achieving cerebral protection in this setting.
Implementing American Heart Association Practice Standards for Inpatient ECG ...Allina Health
Implementing American Heart Association Practice Standards for Inpatient ECG Monitoring: An Interventional Study at Abbott Northwestern Hospital presented by Kristin Sandau, PhD, RN
Matt Anstey is an intensivist from Sir Charles Gardiner hospital in Perth, Australia.
He gave this talk on outcomes after intensive care at an ICN WA meeting in Perth last year.
Effect of hydrocortisone on development of shock amongDr fakhir Raza
effects of hydrocortisone on development of shock among patients with severe sepsis the HYPRESS Randomized Clinical Trial American Medical Association caring for the critically ill patients Surviving sepsis campaign, to determine weather hydrocortisone therapy in patients with severe sepsis prevents the development of septic shock
Trial of decompressive craniectomy for traumatic intracranial hypertension1Dr fakhir Raza
The New England Journal of Medicine, Trial of Decompressive Craniectomy for Traumatic Intracranial Hypertension, Extended Glasgow Outcome Scale (GOS-E), vegetative state, lower severe disability, traumatic brain injury, RESCUEicp,
Presentation slides from our first meeting, held on Tuesday 10th September 2013 at the Royal College of Surgeons.
Find us on
Twitter @STARSurgUK
Facebook.com/STARSurgUK
Email: STARSurgUK@gmail.com
A look at the practicalities, applicability and evidence for medical interventions not currently supported by the guidelines in medical cardiac arrests. Sydney HEMs cardiac education day 9th January 2019.
Prehospital Emergency Anaesthesia in Ambulancenswhems
When weather or hostile scene factors necessitate in-vehicle anaesthesia, it pays to have considered the optimal configuration of personnel, equipment and monitoring. Here is one example.
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These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
Ozempic: Preoperative Management of Patients on GLP-1 Receptor Agonists Saeid Safari
Preoperative Management of Patients on GLP-1 Receptor Agonists like Ozempic and Semiglutide
ASA GUIDELINE
NYSORA Guideline
2 Case Reports of Gastric Ultrasound
Title: Sense of Taste
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the structure and function of taste buds.
Describe the relationship between the taste threshold and taste index of common substances.
Explain the chemical basis and signal transduction of taste perception for each type of primary taste sensation.
Recognize different abnormalities of taste perception and their causes.
Key Topics:
Significance of Taste Sensation:
Differentiation between pleasant and harmful food
Influence on behavior
Selection of food based on metabolic needs
Receptors of Taste:
Taste buds on the tongue
Influence of sense of smell, texture of food, and pain stimulation (e.g., by pepper)
Primary and Secondary Taste Sensations:
Primary taste sensations: Sweet, Sour, Salty, Bitter, Umami
Chemical basis and signal transduction mechanisms for each taste
Taste Threshold and Index:
Taste threshold values for Sweet (sucrose), Salty (NaCl), Sour (HCl), and Bitter (Quinine)
Taste index relationship: Inversely proportional to taste threshold
Taste Blindness:
Inability to taste certain substances, particularly thiourea compounds
Example: Phenylthiocarbamide
Structure and Function of Taste Buds:
Composition: Epithelial cells, Sustentacular/Supporting cells, Taste cells, Basal cells
Features: Taste pores, Taste hairs/microvilli, and Taste nerve fibers
Location of Taste Buds:
Found in papillae of the tongue (Fungiform, Circumvallate, Foliate)
Also present on the palate, tonsillar pillars, epiglottis, and proximal esophagus
Mechanism of Taste Stimulation:
Interaction of taste substances with receptors on microvilli
Signal transduction pathways for Umami, Sweet, Bitter, Sour, and Salty tastes
Taste Sensitivity and Adaptation:
Decrease in sensitivity with age
Rapid adaptation of taste sensation
Role of Saliva in Taste:
Dissolution of tastants to reach receptors
Washing away the stimulus
Taste Preferences and Aversions:
Mechanisms behind taste preference and aversion
Influence of receptors and neural pathways
Impact of Sensory Nerve Damage:
Degeneration of taste buds if the sensory nerve fiber is cut
Abnormalities of Taste Detection:
Conditions: Ageusia, Hypogeusia, Dysgeusia (parageusia)
Causes: Nerve damage, neurological disorders, infections, poor oral hygiene, adverse drug effects, deficiencies, aging, tobacco use, altered neurotransmitter levels
Neurotransmitters and Taste Threshold:
Effects of serotonin (5-HT) and norepinephrine (NE) on taste sensitivity
Supertasters:
25% of the population with heightened sensitivity to taste, especially bitterness
Increased number of fungiform papillae
CDSCO and Phamacovigilance {Regulatory body in India}NEHA GUPTA
The Central Drugs Standard Control Organization (CDSCO) is India's national regulatory body for pharmaceuticals and medical devices. Operating under the Directorate General of Health Services, Ministry of Health & Family Welfare, Government of India, the CDSCO is responsible for approving new drugs, conducting clinical trials, setting standards for drugs, controlling the quality of imported drugs, and coordinating the activities of State Drug Control Organizations by providing expert advice.
Pharmacovigilance, on the other hand, is the science and activities related to the detection, assessment, understanding, and prevention of adverse effects or any other drug-related problems. The primary aim of pharmacovigilance is to ensure the safety and efficacy of medicines, thereby protecting public health.
In India, pharmacovigilance activities are monitored by the Pharmacovigilance Programme of India (PvPI), which works closely with CDSCO to collect, analyze, and act upon data regarding adverse drug reactions (ADRs). Together, they play a critical role in ensuring that the benefits of drugs outweigh their risks, maintaining high standards of patient safety, and promoting the rational use of medicines.
The Gram stain is a fundamental technique in microbiology used to classify bacteria based on their cell wall structure. It provides a quick and simple method to distinguish between Gram-positive and Gram-negative bacteria, which have different susceptibilities to antibiotics
Basavarajeeyam is a Sreshta Sangraha grantha (Compiled book ), written by Neelkanta kotturu Basavaraja Virachita. It contains 25 Prakaranas, First 24 Chapters related to Rogas& 25th to Rasadravyas.
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...kevinkariuki227
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
Explore natural remedies for syphilis treatment in Singapore. Discover alternative therapies, herbal remedies, and lifestyle changes that may complement conventional treatments. Learn about holistic approaches to managing syphilis symptoms and supporting overall health.
New Drug Discovery and Development .....NEHA GUPTA
The "New Drug Discovery and Development" process involves the identification, design, testing, and manufacturing of novel pharmaceutical compounds with the aim of introducing new and improved treatments for various medical conditions. This comprehensive endeavor encompasses various stages, including target identification, preclinical studies, clinical trials, regulatory approval, and post-market surveillance. It involves multidisciplinary collaboration among scientists, researchers, clinicians, regulatory experts, and pharmaceutical companies to bring innovative therapies to market and address unmet medical needs.
4. A big year for airways management in cardiac
arrest
• Airways 2: iGel vs ETT
• PART: Laryngeal tube vs ETT
• Jabra: BVM vs ETT
5.
6.
7.
8.
9. • Large Scale
• Important clinical question
• Patient focused outcome
• Included non adv airway
• SGA group had more adv
airway
• Imbalance in numbers that
received an airway
• Volunteers
• 70% first pass success ett
• Not generalisable to hospital
11. PART- Outcomes
Primary outcome Looking at 72 hour survival
• LT 18.3% vs ETI 15.4%
Secondary outcomes
• Return of spontaneous circulation: LT 27.9% vs ETI 24.3
• Hospital survival: LT 10.8% vs ETI 8.1%
• Favourable neurological status at discharge: LT 7.1% vs ETI 5.0%
Crossover: LT 4.5% vs ETI 9.2%
Success rates: LT 90% vs ETI 52%
18. • Pragmatic
• Blinding and randomisation
• Important question
• Good internal and external
validity
• Patient centred outcomes
• Post ROSC care and CPR
quality not controlled
• Can’t generalise to early ROSC
group
• Loss to follow up
• Not powered to detect
favourable neuro outcome
• Low survival rate
19. • Patient preferences
• Few or different doses
• Applicability to hospital patients
• Different cohorts of patients
• Survival with newer technology
• IV access
• Health economics
20. • Response to airways trials
• Response to adrenaline trial
• Other updates
• Lignocaine in VF/VT
• Magnesium
• Prophylactic antiarrhythmic
24. Take home points
- Type of airway management might not matter so much
- iGEL first is a reasonable strategy
- Good quality CPR and early defibrillation is much more important
- Implications for intubation training
- Adrenaline creates more survivors with severe neurologic impairment
- Lignocaine can be considered in VF/VT
Editor's Notes
Question: In adult patients with non-traumatic out-of-hospital cardiac arrest, does a supraglottic airway device compared with tracheal intubation as the initial advanced airway management strategy, improve functional neurological outcome?
Background
Survival in cardiac arrest is poor, looking for ways to improve
Optimal airway mx uncertain as very little high quality evidence
SGA over last 10 years increased use without good evidence base, ett has been gold standard
SGA is simpler and faster but may be less effective and carry high risk of aspiration
The study
multicentre, cluster randomised, UK, paramedics randomised 1:1 computer random sequence stratified by experience/distance/organisation, voluntary by paras
Paramedic discretion permitted and was necessary for ethics approval, allowed crossover
June 2015- Aug 2017
Exclusion: resus inappropriate, adv airway already in situ, mouth opening less than 2cm
4882 and 4407 patients respectively were included in the primary outcome analysis
Well matched baseline demographics, median age 73, 36% female, median time to para arrival within one min of each other, 50% asystole/22% VF, CPR prior 63%, defib prior 3%
Common: paramedics got extra training, standard airway approach with bvm and adjuncts first, etco2 used
Note this is not testing a device its testing a strategy
Primary outcome
No statistical significant difference in MRS at hospital discharge or 30 days after OOHCA, adjusted risk difference of -0.6% CI -1.6-0.4%
MRS divided into two groups, good and a poor
Secondary outcomes
There was a difference in initial ventilation success on first 2 attempts, 87.4% vs 79% p <0.001
There was a difference in unintentional loss of device 10.6% vs 5% p<0.001
No difference in survival at scene (53.7 vs 56.5%) or at discharge/30d 8% vs 8.4%
No difference in aspiration 15.1% vs 14.9%
No difference in ROSC 30.6% vs 28.4%
Subgroup analysis
Intervention group: Para for igel first, 82% received igel, 15% had no adv airway, 2.4% received ett first
Control group: Ett with dl and bougie 2 person technique recommended, 62% ett first, 22% no airway, 14% airway first
A significant number had no advanced airway, this may be due to many reasons eg by stander defib, short arrest, futility
The patients without an advanced airway did significantly better and made up the majority of good survivors (20% had good outcome)
22% in ETT group and 15% in SGA group had no adv airway? Sway results? Were these patient better?
Could it be that SGA is more appealing to insert? If directed to ETT first you have more patients without adv airway and high number of crossover (600 cf 166 who crossed to ett)…implication of this is that the groups are no longer the same and differential crossover. Were patients more likely to get sga if better outcome predicted, more likely to get ett if looked more sick
Of the patients who did get and airway, prespecified sensitivity analysis (subset so not as reliable)
In patients who received an advanced airway more patients in the SGA group had a good outcome 3.9% vs 2.6%, adjusted OR 1.57 with CI 1.18-2.07
Is this because:
iGel is better
Paramedics more likely to use iGel in less sick patients
Scientifically this is less reliable
Strengths: large scale, important clinical question, patient focussed
Weakness:
trial population included patients that didn’t receive advanced airway
Possible confounding by indication as more received SGA (confounding by indication is when an indication for something also effects the outcome)
Imbalance in numbers 3400 vs 4200 with advanced airways
Paramedics were volunteers, may not be representative, they were also trained more
Not sure of PCI, TTM etc between groups
May not be applicable in physician/paramedic groups or with other types of SGA
70% first pass success, poor, may not be representative of our population, cardiac arrest is hard
Not generalisable to a hospital population
More than 1/3 got no bystander CPR and only 15% received defibrillation (austalia Monash study 60% don’t get bystander CPR)
US study, 27 ED medical services, adults with OOHCA, cluster randomised for 3-5 months, cross over allowed, open label
Patients were enrolled if advanced airway anticipated which is different to airways2 which were already randomised
Laryngeal tube used, different from igel, ? external validity
Intubation via VL or DL, as many goes as would like, rescue technique allowed
Excluded: major bleeding, major facial trauma, asphyxic cardiac arrest, pregnant, prisoners
3004 patietns
Primary outcome Looking at 72 hour survival
18.3% vs 15.4% for lma vs ett, statistically significant, ARR 2.9% p0.04 CI 0.2-5.6%, NNT 35
Secondary
- Return of spontaneous circulation: LT 27.9% vs ETI 24.3 ARR 3.6% in favour of LT (95% CI 0.3% to 6.8%; P = 0.03)
- Hospital survival: LT 10.8% vs ETI 8.1% ARR 2.7% in favour of LT (95% CI 0.6% to 4.8%; P = 0.01)
- Favourable neurological status at discharge: LT 7.1% vs ETI 5.0% ARR 2.1% in favour of LT (95% CI 0.3% to 3.8%; P = 0.02)
Crossover: 4.5% in lt group, 9.2% in ett group
Success rates: 90% LT, 52% ett
Strengths: important question, complex randomisation to minimise group differences, tested strategy not device
Weaknesses: crossover might mean more differences between the groups, lack of blinding, non patient centred outcome, may not be able to generalise beyond LT
External validity
US is going to be different to UK and AUS
ETT success rates of 51% is very different to our practice
A big difference is interesting and supports SGA approach but hard to externally apply
Enrolment raises questions, if clinician has the discretion and knows what plan they are going to go with first, if they aren’t confident or have concerns with the approach they are more likely not to enrol and will go with basic airway manoeuvres.
Not as good as airways2 from a scientific view but supports the results
Adverse events (according to group allocation): More than two attempts at airway insertion LT 4.5% vs ETI 18.9%
Unsuccessful initial airway insertion LT 11.8% vs ETI 44.1%
Unrecognised misplacement or dislodgment LT 0.7% vs ETI 1.8%
Inadequate ventilation LT 1.8% vs ETI 0.6%
Pneumothoraces LT 3.5% vs ETI 7.0%
Rib fractures LT 3.3% vs ETI 7.0%
Multicentre RCT, >2000 patients, France and Belgium, 20 services and emergency physicians present
Didn’t included massive aspiration prior to randomisation, pregnant or prison
Allocated a strategy and allowed for rescue techniques, only stable rosc patients transported, just looking at pre rosc airway
Primary outcome
Survival to favourable outcome at 28 days
4.3% in BVM and 4.2% in ETT, failed to show non inferiority or inferiority ie not difference between the groups
Not externally valid, most patients will have igel or ett in our service to get hands off jaw thrust and freed up but would help providers that only can do basic manoeuvres
Intention to treat, 14% of BVM group get rescue advanced airway which may alter the internal validity of the study and show differences between the groups
Should this change practice
These papers need to be looked at in totality
? Need to filling missing piece of the puzzle sga vs bvm, now more equipoise
Implications of training and maintaining ett skills, this needs to stay in the skill set : too hard for theatres, dilution with more icps, may be different for different areas
Provides reassurance that the move towards igel is not harmful
How does this affect post rosc care and timing of intubation
Overall take home point
Airway may not matter, lots of patients had no adv airway and did well
Hard to justify ETT as first line approach
iGel achieves the same primary outcome, is more likely to ventilate, does not increase regurg/aspiration, is used more commonly by paramedics, if you ask them to use igel they are more likely to use it than ett, crossover suggest igel more applicable (position, single person) and depending on your interpretation may have better outcomes when looking at sensitivity analysis
ETT can’t be thrown away, eg choking patients or failed sga, how do we train for this?
How do we train paramedics
BLS rules, airway shouldn’t detract from this (Ett needs bandwidth, equipment and personel), disadvantage may be nothing to do with tube and everything to do with distraction from bls/defib. Ie which is more harmful rather than which is more beneficial
Adrenaline in cardiac arrest has potential beneficial effects by increasing the aortic diastolic pressure and thus increasing coronary blood flow; however harmful effects have also been hypothesised. These include increased myocardial oxygen demand, and platelet activation leading to thrombosis and impaired microvascular flow potentially increasing cerebral ischaemia. There has been conflicting evidence as to whether epinephrine (adrenaline) is beneficial or not.
9 observational studies showed increased ROSC without improved long term survival, 50% had a reduction in favourable neurologic outcome in those that survived suggesting adrenaline may not help long term favourable neurologic outcome.
Study
16 years old, NHS, excluded asthma and anaphylaxis, excluded those already received adrenaline/pregnant/trauma, double blinded
8000 patients
Primary: survival at 30 days Secondary: favourable neurologic outcome at different time points up to 3 months
Similar baseline characteristics
Age: 69.7 (Epinephrine) vs. 69.8 (Placebo) Male: 65.0% vs. 64.6% Initial Cardiac Rhythm: Shockable: 19.2% vs. 18.7% VF: 17.8% vs. 17.1% VT: 0.6% vs. 0.5%
Non-shockable: 78.4% vs. 79.5%, Asystole: 53.2 % vs. 54.9%, PEA: 23.8% vs. 23.4%
Cause :
Medical: 91.1% vs. 92.3%, Traumatic: 1.6% vs. 1.4%, Drowning: 0.2% vs. 0.3%, Drug Overdose: 1.8% vs. 1.8%, Electrocution: 0 vs. <0.1%, Asphyxia: 2.9% vs. 2.0%, Missing Data: 2.3% vs. 2.1%
Witness
Unwitnessed: 37.3% vs. 37.6%, Bystander: 50.1% vs. 49.2%, Paramedic: 11.3% vs. 11.8%, Missing Data: 1.3% vs. 1.4%
CPR
- Bystander: 59.3% vs. 58.7%, Paramedic 11.3% vs. 11.8%, Missing Data: 1.7% vs. 2.1%
Time frames for key events also similar
Median interval between emergency call and ambulance arrival: 6.7 min (Epinephrine) vs. 6.6 min (Placebo)
Median interval between emergency call and administration of trial agent: 21.5 min vs. 21.1 min
Mean interval between ambulance arrival and departure: 50.1 min vs. 44.5 min
Mean interval between ambulance departure and hospital arrival:12.9 min vs. 12.4 min
Medial interval between initiation and cessation of ALS: 47.5 min vs. 43.1 min
Mean of 4.9 drug doses given in epinephrine group vs. 5.1 in placebo
5% received amiodarone in epinephrine group vs. 9.2% in placebo
3980 shocks after randomisation in epinephrine group vs. 3962 in placebo
Initial Response to Resuscitation
- Transported to hospital in 50.8% in epinephrine group vs. 30.7% in placebo
- Of those transported 15.3% of epinephrine group not declared dead in emergency room vs. 7.3% in placebo group
Rates of concurrent pre-hospital treatments (IV or IO access, supraglottic airway device, endotracheal tube) similar
PRIMARY: Primary outcome adrenaline had a significantly higher survival at 30days 3.2 vs 2.4, NNT 112 to prevent one death, ARR 0.89 CI 0.17-0.16
SECONDARY: No significant difference in favourable neurologic outcome 2.2 vs 1.9, higher likelihood of disability in those that achieved rosc in adrenaline 31% vs 17.8%
ROSC 36.3 vs 11% rosc rate in adrenaline group
Shock vs no shock
Sub group of presenting rhythm showed no difference in shock vs non shock, would have thought pea might do better with adrenaline but wasn’t born out. Only observational data exists in good for pea/asystole and bad for VF/VT
Survival rates at various time points were significantly better in the Epinephrine group. Length of stay in ICU and hospital did not differ
Neurological outcomes were possibly worse in the Epinephrine group when categorised into binomial ‘favourable’ and ‘non-favourable’ there was no statistically significant difference
When assessing the number who survived with severe neurological deficit, the difference was statistically significant with worse outcome in the Epinephrine group
The pre-hospital use of epinephrine in patients with OOHCA resulted in a significantly higher rate of survival at 30 days when compared to a placebo
There was no significant difference between groups with regards to a favourable neurological outcome
More survivors in the epinephrine group had severe neurological impairment.
Strengths
- pragmatic, good blinding and randomisation, important question, good internal and external validity, patient centred outcomes,
Weaknesses
CPR quality/post ROSC care not controlled: given blinding unlikely to affect performance bias
Can’t generalise to early ROSC group
There was significant loss to follow-up for the secondary outcomes 20 (18.2%) in the placebo group and 29 (18.2%) in the epinephrine group were lost at 3 months, attrition bias if there are differences in the groups lost to follow up… ie what if more placebo had sev neuro def
For the survivors, there was a difference in the rate of unfavourable neurological outcome at hospital discharge (epinephrine 31.0% vs placebo 17.8%) and at 3 months (16.3% vs 14.9%), so what is the best time frame to study neurological outcomes
- Is this because patients with unfavourable are dying before 3 months, what is the best time point to assess?
Not powered to find statistically significant favourable neurologic outcome, ? Larger trial would have been different
Lower survival rate than would be expected, probably because patients get rosc before enrolement so this would select worse patients, particularly in shockable rhythm
Patient preferences: 95% said long term survival without brain damage most important rather than surviving at all, how do we consider individual preferences
On average patients got 5 adrenaline, would you consider stopping earlier?
Can this be applied to in hospital? Different patients/aetiology/survival rates/response time/personnel
Doesn’t explain different groups/patients/aetiology who may benefit from adrenaline
Will adrenaline be helpful in survival to ecmo and change outcomes that way?
What about different doses?
Could iv access and adrenaline vs no iv access and no adrenaline affect outcomes, less cpr interruption
Lingering health economics questions: survival to hospital/ICU/organ donation/DC
Where to now
CPR and adrenaline much more important, confusion about treatment shouldn’t interfere with CPR/adrenaline and protocols should be followed without discussion!
Await ilcor updates
Need more public conversation about whats important and this is what should drive change
Enhancing community response, bystander CPR and defib
When things are being done serial not parallel, adrenaline can move down the list without worsening outcomes significantly
New model for ILCOR recommendations, continuous evidence evaluation processes. ANZIC guidelines not yet changed
Adrenaline: The study did not demonstrate improved long-term survival with good neurologic function. The optimal dose and timing of epinephrine during cardiac arrest remain important knowledge gaps. Moving forward, the ILCOR ALS Task Force will evaluate the results of this important study and determine if the current ILCOR treatment recommendations for epinephrine during CPR should be modified.
Airways: 2015 ILCOR Treatment Recommendation: We suggest using either an SGA or tracheal tube as the initial advanced airway during CPR (weak recommendation, very low-quality evidence) for cardiac arrest in any setting. The Task Force will combine the findings from these trials with those from previously published trials to generate an updated consensus on science and treatment recommendation.
Lignocaine: amiodarone OR lignocaine may be consider for VF/pVT that is unresponsive to defibrillation. 2015 said amiodarone may be considered.
Magnesium: The routine use of magnesium for cardiac arrest is not recommended in adult patients (same as 2015)
Magnesium may be considered for torsades de pointes (ie, polymorphic VT associated with long QT interval) (Class IIb, LOE C-LD). The wording of this recommendation is consistent with the AHA’s 2010 ACLS guidelines.
Post rosc care prophylactic antiarrhythmic: 2018 recommendations: insufficient evidence to support or refute the routine use of lidocaine early (within the first hour) after ROSC. In the absence of contraindications, the prophylactic use of lidocaine may be considered in specific circumstances (such as during emergency medical services transport) when treatment of recurrent VF/pVT might prove to be challenging (Class IIb, LOE C-LD).
Intraosseous vascular access is associated with lower survival in patients with OOHCA
Secondary analysis of previously collected database in the states, 6 centres, huge data set
Excluded either failed IO or IV or had both an IV/IO, only looked at initial IV or IO patients
Primary: favourable neurologic outcome MDR <4
Looked at AED use, timing, bystander etc at baseline
13000 oohca included, only 660 received IO, massively weighted towards IV
IO had a 1.5% advantage, IV had 7.6% advantage
Multivariate regression, IO associated with poorly outcome, 0.24 with CI 0.12-0.46 (odds of IO have good outcome 24% that of IV)
Should we be throwing IO in the bin?
6% difference seems to be too large and unusual just for IO especially given the drugs used in cardiac arrest aren’t necessarily that import
Especially if the finding from the resuscitology paper puplished earlier this year
Makes you think about those patients that are getting IO
High stress environment more likely to reach for IO
IV might be done in patients that aren’t so bad and have decent vascular ? less sick (if you can have this in cardiac arrest)
No matter how much statistics you do its difficult to balance the groups
Shockable in IV 26% vs 14% in IO, witnessed in 41% vs 35%, IV had higher rates of hypothermia and pci. Stats can account for some of these but not the decisions that were made for these patients, paramedics or docs are seeing something the numbers don’t and going for IO instead
Reasonable to try IV first otherwise go for IO
Resucutiology: drugs more likely to reach the heart significantly faster when delivered through a humeral IO than brachieal vein
Hyperoxia
Association between intra and post arrest hyperoxia on mortality in adults with cardiac arrest, resuscitation, patel, systematic review
Intra-arrest not just post arrest
2000-2015, adults, pao2 recorded, mortality end point, in hospital and prehospital looked at
40000 patients, 16 observational studies, 119-12000 patients included, very different study weighting
Only 2 studies looked at intra-arrest, approx. 300 patients
4 studies abg in an hour, 1 study in 4 hours, 8 studies in 24 hours…. Not at the point of rosc so not necessarily that relevant
Varying definitions for hyperoxia: 300mmhg seems to be standard
Outcome: intra-arrest, hyperoxia showed lower mortality, OR 0.25, CI don’t cross 1 (significant), for post arrest hyperoxia is bad OR 1.34, not statistically significant
Intraarrest hyperoxia good, post arrest bad
Titrate down when stable to reach normoxia
Intra-arrest evidence not good enough to change practice but it does show we shouldn’t mess around with oxygen during arrest and focus on the resuscitation however likely more evidence to come with hyperoxia
All observation, so many potential confounders, timing of hyperoxia not measured so not able to apply to your practice, huge changes to resus care during 2000-2015 so likely too many other confounders impossible to draw out from retrospective and observational data
Resuscitation, Sin Young Kim et al, how much experience do rescuers require to achieve successful tracheal intubation during cardiopulmonary resuscitation
Prior studies suggest around 100 intubations to get core skills then approx. 1 per month
ED residents, adult, direct, cardiac arrest patients, south korea, retrospective data collected prospectively
Randomly assigned to cpr or ett, data from cctv from arrest and ecg data which helps assess interprutption timing
Main outcomes: qualified Ett intubation in 60sec, highly qualified 30s without complications, secondary: first pass success and hands of chest time
Time is entering mouth to bag ventilation time
255 patients in total, 162 excluded either VL used, DNR or previously placed airway, 110 attempts for 93 patients (small)
First pass success is 68%, 11 from 110 were oesophageal (high, ? not reflective of practice)
For 80% of qualified ett without complication it would require 137 intubations, to get to 90% 157 intubations, for highly qualified it would require 220 intubations and for 90% 243
Strengths
Good registry, prospective, video and timings used, reasonable methodology, internal validity reasonable
Weakness
Single centre, external validity, huge number removed ? VL and difficult airways, only 11 clinicians used, only 110 patients (small patient, small clinician), can’t really generalise this, doesn’t really change practice
Training and competence needs to be on the radar