Zworth Reading
EMMax’s EM Weekly Update
Highlight of the Week
Is non-supine positioning preferable in patients requiring intubation in the emergency department?
Emergency Medicine Journal (Best Evidence Topic report) · Best Evidence Topic (BET) review
BET review of 6 ED intubation studies (4 observational, 2 RCTs; 15,984 pooled intubations) examining whether non-supine (inclined, ramped, head-up, or upright) positioning improves first-pass success versus supine positioning. Across the included studies, non-supine positioning was non-inferior or superior to supine, with a positive association between angulation and first-pass success in 3 of the studies. The authors align with the 2025 Difficult Airway Society guideline recommending 30° head-up positioning. BET clinical bottom line: inclined positioning should be used in ED intubation if the patient does not require C-spine immobilisation.
'Is ramping better?' is not really the right question. In practice, most of us aren't debating this in every patient, we're already ramping in specific populations where the physiologic rationale is strong (obese, OSA, acute respiratory failure, pulmonary oedema, neuroprotective intubations). For those patients, this BET is a reasonable reinforcement rather than new information. Methodologically it's a BET, not a full systematic review — 6 studies, only 2 randomized, no pooled effect estimate, no formal quality assessment. That's fine for what a BET is, but it means the conclusion 'supports protocolised use' is a bit stronger than the evidence provides on its own. Where I do give this weight is in the airway-management space, where accumulated expert consensus, physiologic rationale, and the DAS guideline all point in the same direction as the trial signal.
Bottom line: Doesn't really change practice for me. It's a reasonable reminder to continue ramping in the patient populations where you'd already be considering it (obese, OSA, respiratory failure, pulmonary oedema, neuroprotective intubations).
Important EM Papers
Ventilation parameters during Advanced Life Support in cardiac arrest (CAvent): A multicentre observational cohort studyLOE 3 (Prospective observational)
Resuscitation
In adult out-of-hospital cardiac arrest (OHCA) patients receiving manual ventilation during CPR, what are the actual delivered tidal volumes and airway pressures across different airway devices (bag-valve-mask [BVM], supraglottic airway device [SAD], endotracheal tube [ETT]) and ventilation modes (synchronous vs asynchronous)?
241 OHCA patients across 5 Advanced Life Support (ALS) systems in Sweden and the Netherlands, 28,120 ventilations captured via portable pneumotachograph. Median expiratory tidal volumes: synchronous BVM 186 mL (95% CI 104-260), asynchronous BVM 93.7 mL (95% CI 31.2-155), synchronous SAD 395 mL (316-475), asynchronous SAD 333 mL (227-437), asynchronous ETT 404 mL (371-435). Asynchronous ETT ventilation produced the highest peak airway pressures (51.0 cmH2O, 95% CI 48.7-53.1) and the most time above 30 cmH2O (5.8 sec/min, 95% CI 5.1-6.4).
Large-scale objective measurement of what actually gets delivered during real-world resuscitations. Important caveat: this is a physiologic/parameter study, not a patient-centered outcomes study. It does not tell us whether these ventilation differences translate into ROSC, survival, or neurologic outcome. Figure 2 is where the most important data lives, and honestly the confidence intervals are wide enough that firm conclusions are hard to draw from any single number. The synchronous BVM tidal volume of 186 mL is striking on its face but the CI (104-260) is huge. Where I do think this is signal, not noise, is (a) BVM ventilation during CPR often delivers substantially less than intended, and (b) asynchronous bagging through an ETT can generate quite high peak pressures, which has implications for gastric insufflation and preload.
Bottom line: Not practice-changing but worth knowing. Two clinical takeaways: (1) BVM ventilation during CPR is probably less effective than we assume, which reinforces the value of getting to a definitive airway when circumstances allow; (2) once you have an ETT in and are ventilating asynchronously, you're generating higher pressures than intuition suggests, and a lighter hand on the bag is probably a good idea. My personal practice is to stick with 30:2 until the patient has a supraglottic or is intubated, though newer protocols support asynchronous compressions/ventilation earlier in the interest of simplicity and continuous compressions.
FOAM Radar
HFNC vs. NIV in Acute Cardiogenic Pulmonary Edema: Go with the Flow?Knowledge translation / critical appraisal
REBEL EM · LOE 2 (RCT) being appraised
REBEL EM appraises an RCT comparing high-flow nasal cannula (HFNC) with non-invasive positive-pressure ventilation (NIPPV) as first-line respiratory support in acute cardiogenic pulmonary oedema (ACPE), looking at reduction in respiratory rate and distress in the first 2 hours.
Bottom line: Useful critical appraisal, appropriately cautious in its conclusions. The underlying trial has limitations, but HFNC appears to be a safe alternative to NIPPV in ACPE as long as you have the ability to escalate if the patient doesn't respond. Not a call to abandon NIPPV, but a reasonable option for the patient who can't tolerate the mask.
The Case of the Malignant CohortCommentary / critical appraisal
EMCrit (EM Nerd) · Appraisal of a Level 2 RCT (Hydra Trial, JAMA 2026)
Spiegel takes on the Hydra Trial (YEARS algorithm in cancer patients — the highlight of last week's newsletter) and makes some sharp Bayesian points. Two things worth carrying: (1) 275 of 352 patients (78.1%) in the YEARS arm still ended up getting a CTPA, so the large majority of patients in both arms received chest imaging regardless of assigned strategy. (2) The baseline VTE rate in the Hydra cohort was surprisingly high even in patients scoring 0 on YEARS (~10%), which suggests YEARS did not risk-stratify this population as effectively as it does in general-population cohorts. Spiegel's overall conclusion: it is probably safe to use YEARS in cancer patients, but you should accept a slightly higher posterior risk than you would tolerate in a general-population patient.
Bottom line: Great piece and a great reminder of Bayesian thinking (pretest probability really does matter, and a decision rule performs differently when it's applied to a higher-prevalence population). Definitely worth reading in conjunction with the Hydra Trial itself.Iit doesn't undo the conclusion that YEARS is safe in cancer patients, but it appropriately calibrates our expectations of how much CT-avoidance you can actually achieve in this group.
Major Journals Scan
Hip Fractures: A ReviewLOE 5 (Narrative review)
JAMA
Why it matters to EPs: Hip fractures are a bread-and-butter ED presentation. This review covers classification, prognosis, and post-acute management. Useful background for counselling patients and families, and for the context behind why ortho pushes for early time-to-OR.
Key numbers: 22% median 1-year mortality, 42-71% regain baseline ADLs at 6 months. Men have higher 1-year mortality (26.9%) than women (18.5%). Risk factors include age (HR 1.35 per 5-year increase), low bone mineral density, prior fracture, and fall risk factors. Post-surgical care should include physiotherapy, fall reduction strategies, and antiresorptive therapy.
Solid JAMA clinical review. Nothing here is new or surprising, but it's a useful refresher on the epidemiology and downstream care. The mortality statistics are worth knowing. The emphasis on post-fracture osteoporosis treatment is important for the whole care pathway but largely outside our lane in the ED.
Bottom line: Good background reading. The 22% one-year mortality figure is worth remembering when discussing prognosis with families of the frail elderly patient with a hip fracture. Otherwise, this confirms what you already know.
Methodology Flag
Critical Care Medicine
Getting attention because it uses 'target trial emulation' (sophisticated methodology that sounds like an RCT) to compare lidocaine and amiodarone in shockable arrest. Point estimate favours lidocaine by 2.8 percentage points for survival.
- Still observational data (ROC CARES registry 2011-2015). Target trial emulation reduces confounding but cannot eliminate unmeasured confounders like arrest etiology, drug timing relative to ROSC, and provider experience.
- The confidence interval crosses zero (-0.6 to 6.2%). The data are as consistent with 'no difference' as with 'meaningful benefit for lidocaine.'
- Time zero is defined as first antiarrhythmic administration, introducing immortal time bias. Patients had to survive long enough to receive the drug.
- Registry data are now 10+ years old; resuscitation practice has evolved.
What it does contribute: Methodologically thoughtful and honest about its limits. The direction is consistent with the ALPS trial (also showed a non-significant trend favouring lidocaine), adding to the evidence base that amiodarone is not clearly superior to lidocaine.
Bottom line: This confirms equipoise, not superiority. If you generally use amiodarone, no reason to switch based on this study. If you use lidocaine, no reason to feel behind.