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Daily Report

Daily Anesthesiology Research Analysis

07/28/2026
3 papers selected
185 analyzed

Analyzed 185 papers and selected 3 impactful papers.

Summary

Today’s most impactful anesthesiology-related studies addressed virtual preoperative consultation, evidence standards for acute kidney injury biomarkers, and ventilatory management during general anesthesia. Together, they emphasize pragmatic comparative effectiveness, reporting quality, and the need to avoid assuming that physiologically plausible interventions improve postoperative outcomes.

Research Themes

  • Virtual versus in-person preoperative anesthesiology consultation
  • Standardization of diagnostic biomarker research
  • Randomized evaluation of intraoperative ventilatory settings

Selected Articles

1. Comparative effectiveness of virtual versus in-person anaesthesiology consultations: the VIRTUAL retrospective cohort study.

81.5Level IICohort
British journal of anaesthesia · 2026PMID: 42509157

This retrospective comparative-effectiveness study emulated a target trial among 17,027 adults with ASA physical status III or higher undergoing moderate- to high-risk elective noncardiac surgery. Noninferiority of virtual consultation for 90-day major morbidity or mortality was inconclusive, whereas length of stay, costs, and days alive and at home were noninferior, with lower carbon emissions associated with virtual care.

Impact: This is one of the largest real-world evaluations of virtual preoperative anesthesiology consultation and directly addresses whether rapid expansion of telemedicine compromises perioperative safety. Its inconclusive primary result is clinically informative because it supports selective implementation rather than universal substitution of in-person assessment.

Clinical Implications: Virtual consultations may be appropriate for selected patients and healthcare pathways, particularly when access, travel burden, or sustainability is important. High-risk patients should not automatically be shifted to virtual assessment until triage criteria and additional safety data are established.

Key Findings

  • Among 17,027 patients, the primary 90-day major morbidity or mortality outcome occurred in 26.3% after virtual consultation versus 24.9% after in-person consultation.
  • Noninferiority for the primary outcome was inconclusive in both instrumental-variable and propensity-score analyses.
  • Virtual consultation was noninferior for length of stay, costs, and days alive and at home, and was associated with reduced carbon emissions.

Methodological Strengths

  • Large population-based cohort of at-risk surgical patients.
  • Target trial emulation with both instrumental-variable and propensity-score analyses to address measured and unmeasured confounding.

Limitations

  • Retrospective observational design limits causal inference.
  • The primary noninferiority conclusion remained inconclusive, and findings may depend on local telemedicine infrastructure and triage practices.

Future Directions: Future studies should prospectively evaluate risk-stratified triage algorithms, assess patient subgroups that require physical examination, and determine whether hybrid consultation pathways can preserve safety while maximizing access and environmental benefits.

BACKGROUND: Virtual care is increasingly used for preoperative assessment. We aimed to estimate the noninferiority of virtual vs in-person anaesthesiology consultations with respect to 90-day morbidity and mortality in at-risk adults having noncardiac surgery. METHODS: We conducted a retrospective observational comparative effectiveness study using a target trial emulation framework. Eligible participants were aged ≥40 yr, with an ASA physical status ≥3, having elective, noncardiac, non-orthopaedic, moderate- to high-risk surgery, and attended a preoperative anaesthesiology consultation in Ontario, Canada, between October 2020 and March 2022.

2. STARDaki: a consensus-based STARD extension for standardized reporting of diagnostic accuracy in acute kidney injury.

78.5Level ISystematic Review
Intensive care medicine · 2026PMID: 42517928

This systematic review and modified Delphi consensus study evaluated 122 acute kidney injury biomarker diagnostic-accuracy studies. Reporting quality was poor: only 16 studies were judged high quality by QUADAS-2, and compliance with STARD was insufficient for meta-analysis. The international expert panel developed STARDaki, extending STARD guidance with criteria for patient selection, reference standards, and test-retest reliability.

Impact: Rather than promoting another biomarker, this paper addresses a foundational problem: unreliable and non-comparable evidence generation. STARDaki could improve reproducibility, reduce exaggerated diagnostic estimates, and make future acute kidney injury biomarker studies more clinically actionable.

Clinical Implications: Clinicians and investigators should require transparent reporting of patient selection, timing of sampling, reference standards, and test-retest reliability before adopting AKI biomarkers. Regulatory, guideline, and journal processes may use STARDaki to improve evidence appraisal.

Key Findings

  • The review identified 122 diagnostic-accuracy studies of AKI biomarkers.
  • Of 107 sufficiently reported studies, only 19 evaluated AKI diagnosis within 48 hours of sampling and only 16 were considered high quality by QUADAS-2.
  • Low STARD compliance prevented meta-analysis, leading the expert panel to establish STARDaki criteria for patient selection, reference standards, and test-retest reliability.

Methodological Strengths

  • Combined systematic assessment of published diagnostic studies with QUADAS-2 and STARD 2015 evaluation.
  • International 17-member modified Delphi process linking empirical quality assessment to consensus reporting standards.

Limitations

  • The low quality and heterogeneity of the underlying studies prevented quantitative meta-analysis.
  • Consensus recommendations require external validation and may evolve as AKI biomarker methodology advances.

Future Directions: Prospective multicenter studies should apply STARDaki from protocol development through publication, with standardized reference standards, prespecified sampling windows, external validation, and test-retest assessments.

INTRODUCTION: Biomarkers have been identified to predict, diagnose and prognosticate acute kidney injury (AKI) but existing studies are heterogenous and contradictory. OBJECTIVE: To compare diagnostic performance of AKI biomarkers, evaluate the quality of AKI biomarker studies and to develop standards for reporting studies of diagnostic test accuracy (DTA) of AKI biomarkers. METHODS: A systematic literature review was conducted to identify studies focusing on the diagnostic performance of AKI biomarkers published before February 2025. Retrieved DTA studies were assessed for methodological quality and completeness using the QUADAS-2 and Standards for Reporting Diagnostic Accuracy (STARD) 2015 checklists.

3. Positive End-Expiratory Pressure, Tidal Volume, and Fraction of Inspired Oxygen During General Anaesthesia in High-Risk Patients-A Randomised Clinical Feasibility Trial.

75.5Level IRCT
Acta anaesthesiologica Scandinavica · 2026PMID: 42508987

This multicenter randomized factorial feasibility trial included 483 ASA physical status III to V patients undergoing major surgery under general anesthesia. The study achieved separation between ventilatory interventions but did not meet its feasibility targets. Most postoperative outcomes did not differ, while higher PEEP levels were associated with more arrhythmias and lower inspired-oxygen targets were associated with more intraoperative hypoxemia.

Impact: The study challenges the assumption that higher PEEP or lower oxygen exposure is automatically beneficial in high-risk surgical patients. Its negative and feasibility findings are valuable for designing definitive trials and caution against routine escalation of ventilatory settings without patient-specific justification.

Clinical Implications: Routine use of higher PEEP should be approached cautiously in high-risk patients because of a possible arrhythmia signal. Oxygen targets should be individualized, with close monitoring for hypoxemia when lower inspired-oxygen concentrations are used.

Key Findings

  • The multicenter randomized trial enrolled 483 ASA physical status III to V patients across eight Danish hospitals.
  • Intervention separation was achieved, but predefined feasibility goals were not met.
  • Most postoperative outcomes were similar; arrhythmias appeared more frequently with PEEP 8 or 10 cm H2O, while lower FiO2 targets were associated with more intraoperative hypoxemia.

Methodological Strengths

  • Multicenter randomized factorial design across eight hospitals.
  • Evaluation of several clinically relevant ventilatory parameters in a high-risk surgical population with registered trial methodology.

Limitations

  • The trial was designed primarily for feasibility and did not meet its predefined feasibility goals.
  • The sample size was insufficient to establish effects on uncommon major postoperative complications or mortality.

Future Directions: A larger definitive multicenter trial should use the observed feasibility data to refine protocol adherence, stratify patients by pulmonary and cardiovascular risk, and prospectively assess clinically important pulmonary, cardiac, and patient-centered outcomes.

BACKGROUND: Optimal ventilatory settings during general anaesthesia are unknown. The goal of this trial was to test different ventilatory settings and blood pressure targets during general anaesthesia. This manuscript focuses on the ventilatory interventions. METHODS: This was a multicentre, randomised factorial trial conducted at eight hospitals in Denmark. Four hundred and eighty-three patients ASA 3-5, scheduled for major surgery under general anaesthesia, were included. Patients were randomised to positive end-expiratory pressure (PEEP) of 5, 8, or 10 cm H