Daily ReportOct 14, 2026
Anesthesiology, October 14 edition
We read 51 papers and selected 3.
Summary
Today's most impactful studies address opioid-sparing regional anesthesia, objective monitoring of anesthetic depth, and occupational noise exposure in operating rooms. A randomized trial demonstrated clinically meaningful benefits from the serratus posterior superior intercostal plane block after open cardiac surgery, while a large randomized volunteer study refined the relationship between the Bispectral Index and responsiveness across volatile anesthetics. A systematic review quantified persistent intraoperative noise exposure substantially above World Health Organization recommendations.
Research Themes
- Opioid-sparing regional anesthesia and enhanced recovery
- Validation of processed electroencephalographic monitoring
- Occupational safety and operating-room environmental exposure
Selected Articles
1. Characterization of the Bispectral Index in Healthy Volunteers Receiving Inhalation Anesthetics in Combination With Opioids in a Randomized Trial.
This randomized volunteer study evaluated BIS values and responsiveness across sevoflurane, desflurane, and isoflurane regimens, with selected opioid combinations. BIS50 values ranged from 67.5 to 76.2 and BIS95 values from 49.1 to 63.3; BIS alone had an area under the receiver operating characteristic curve of at least 0.95 for predicting responsiveness. Opioids added to sevoflurane had minimal influence, whereas desflurane produced somewhat lower BIS thresholds.
Impact: The study provides experimentally controlled calibration data for a widely used anesthetic monitor and demonstrates that a single BIS target should not be assumed to represent identical clinical states across volatile agents. This supports more nuanced interpretation of processed electroencephalographic monitoring.
Clinical Implications: BIS can provide useful information about responsiveness during volatile anesthesia, but clinicians should interpret thresholds in the context of the specific anesthetic agent and clinical setting. The findings do not justify applying these values directly to patients under surgical stimulation or to older or medically complex populations.
Key Findings
- BIS50 ranged from 67.5 to 76.2 across anesthetic regimens, while BIS95 ranged from 49.1 to 63.3.
- BIS predicted responsiveness strongly, with area under the receiver operating characteristic curve values of at least 0.95.
- Adding remifentanil or fentanyl to sevoflurane had minimal impact on BIS50 and BIS95, while desflurane was associated with slightly lower values.
Methodological Strengths
- Prospective randomized allocation across five controlled anesthetic regimens.
- Stepwise end-tidal concentration increases and repeated assessment of both BIS and responsiveness.
- Use of logistic regression to estimate BIS50 and BIS95 with predictive performance analysis.
Limitations
- The analyzed sample was 143 participants rather than the 211 randomized volunteers.
- Participants were young, healthy volunteers without sustained noxious surgical stimulation.
- Findings may not generalize to patients with comorbidities, older adults, or clinical anesthesia with surgery.
Future Directions: Clinical studies should validate agent-specific BIS thresholds during surgery, in older and critically ill patients, and under combinations of opioids, neuromuscular blockers, and other anesthetic agents. Research should also examine whether individualized BIS interpretation improves outcomes rather than merely predicting responsiveness.
BACKGROUND: Processed electroencephalogram (pEEG) monitors are commonly used in anesthesia practice. The relationship between the pEEG and clinical levels of sedation over anesthetic concentrations with and without opioids is not well understood. The purpose of this trial was to investigate the relationship between Bispectral IndexTM (BISTM), clinical measures of sedation, and inhaled anesthetics across a range of anesthetic concentrations and hypnotic states with and without intravenous opioids. METHODS: This prospective, randomized trial enrolled 211 healthy volunteers. Participants were randomized to one of five anesthetic regimens: sevoflurane, sevoflurane with remifentanil, sevoflurane with fentanyl, desflurane, or isoflurane. Target anesthetic end-tidal concentrations were increased in a stepwise fashion until a BIS index of 30 to 40 was reached. At each targeted end-tidal concentration, responsiveness was assessed using the Modified Observer's Assessment of Alertness/Sedation (MOAA/S) score and the BIS index was recorded.
2. Serratus Posterior Superior Intercostal Plane Block Versus Superficial Parasternal Intercostal Plane Block With Local Infiltration for Postoperative Analgesia in Open Cardiac Surgery: A Randomized Controlled Trial.
In this randomized controlled trial, bilateral serratus posterior superior intercostal plane block reduced 24-hour opioid consumption by 20.1 mg morphine milligram equivalents compared with an active comparator targeting both the sternum and drain sites. Pain scores improved from 2 hours onward, and Quality of Recovery-15 scores were 10 points higher, exceeding the minimal clinically important difference. These benefits were observed despite substantial post-randomization exclusions.
Impact: This study compares a relatively broad anatomical regional technique with an active multimodal comparator and demonstrates both opioid reduction and a patient-centered recovery benefit. The effect size exceeded a prespecified clinically important threshold, supporting further evaluation within enhanced recovery pathways.
Clinical Implications: SPSIPB may be considered as a component of multimodal analgesia after median sternotomy, particularly when reducing opioid exposure and improving early recovery are priorities. Adoption should be accompanied by ultrasound-guided training and confirmation in larger, multicenter trials.
Key Findings
- Twenty-four-hour opioid consumption was 36.6 mg versus 56.7 mg morphine milligram equivalents with SPSIPB versus control, respectively; mean difference 20.1 mg, P < 0.001.
- Pain scores were lower with SPSIPB during coughing from 2 hours onward and at rest at 4, 8, and 24 hours.
- Median Quality of Recovery-15 was 119 versus 108, a 10-point difference that exceeded the minimal clinically important difference.
Methodological Strengths
- Prospective randomized controlled design with blinded outcome assessment.
- Active comparator addressed both sternal and chest-drain pain rather than using an inactive control.
- Patient-centered recovery and opioid consumption were assessed alongside pain scores.
Limitations
- Single-center study with only 76 randomized participants and 64 analyzed after exclusions.
- Twelve patients were excluded after randomization, with unequal exclusions between groups.
- Most comparisons other than the registered primary outcome were exploratory.
Future Directions: Multicenter trials should confirm the analgesic and recovery benefits, evaluate block-related complications and diaphragmatic effects, and compare SPSIPB with other contemporary regional techniques within standardized enhanced recovery protocols.
OBJECTIVES: Postoperative pain after open cardiac surgery arises from both sternotomy and chest drains and is often inadequately controlled by anatomically limited techniques. This study compared the serratus posterior superior intercostal plane block (SPSIPB, C3-T10 spread) with superficial parasternal intercostal plane block (PSIPB) plus chest drain-site infiltration. DESIGN: Prospective, randomized, controlled trial with blinded outcome assessment. SETTING: Single-center tertiary referral cardiac surgery center. PARTICIPANTS: Adults undergoing elective open cardiac surgery via median sternotomy; 80 assessed for eligibility, 76 randomized. INTERVENTIONS: Bilateral SPSIPB (n = 35) or bilateral PSIPB plus local anesthetic infiltration at mediastinal and pleural chest drain sites (n = 41), performed preoperatively under ultrasound guidance. MEASUREMENTS AND MAIN RESULTS: The primary outcome was cumulative 24-hour opioid consumption (morphine milligram equivalents, MME); the registered secondary outcomes were Numerical Rating Scale (NRS) pain scores at rest and on coughing and the Quality of Recovery-15 (QoR-15) at 24 hours.
3. Operating room noise levels in anaesthesia a systematic review and meta-analysis.
This systematic review included 50 studies and meta-analyzed 43 datasets, finding a pooled mean intraoperative noise level of 70.7 dB(A), substantially above the World Health Organization recommended hospital exposure level of 35 dB(A). Otolaryngology and orthopaedics had the highest pooled exposures, and surgical specialty significantly predicted mean noise level. The study establishes a quantitative basis for targeted environmental and occupational-safety interventions.
Impact: The paper addresses a pervasive but under-measured occupational and patient-safety hazard and synthesizes data across surgical specialties. Its specialty-specific estimates can guide targeted noise-reduction interventions and future studies linking exposure to clinical performance and patient outcomes.
Clinical Implications: Hospitals should consider routine standardized noise measurement, particularly in otolaryngology and orthopaedic operating rooms. Interventions may include equipment and alarm management, communication protocols, staff education, architectural mitigation, and evaluation of effects on vigilance, communication, and patient safety.
Key Findings
- Fifty studies met the systematic review criteria, and 28 studies contributed 43 unique datasets to the meta-analysis.
- The pooled random-effects mean intraoperative noise level was 70.7 dB(A), with a 95% confidence interval of 69.0-72.3.
- The highest pooled exposures occurred in otolaryngology at 78.8 dB(A) and orthopaedics at 73.3 dB(A); surgical specialty significantly predicted exposure.
Methodological Strengths
- Searches across five databases with systematic review methods aligned with PRISMA guidance.
- Use of validated sound meters and time-weighted mean measurements for meta-analysis eligibility.
- Risk-of-bias assessment by two authors and meta-regression examining specialty-related heterogeneity.
Limitations
- Only 28 of the 50 included studies provided datasets suitable for quantitative pooling.
- The review quantified noise exposure but did not establish causal effects on patient outcomes or clinician performance.
- Measurement methods, operating-room conditions, and sampling durations likely contributed to residual heterogeneity.
Future Directions: Prospective multicenter studies should use standardized continuous monitoring and evaluate whether noise-reduction interventions improve communication, cognitive performance, teamwork, error rates, and patient outcomes. Research should also define clinically meaningful exposure thresholds rather than relying solely on environmental recommendations.
BACKGROUND: Intraoperative noise is an occupational hazard with the potential to compromise anaesthetist performance and patient safety. The WHO recommends hospital sound exposure ≤ 35 dB LAeq (A-weighted equivalent continuous sound level), yet noise levels routinely exceed this level. This systematic review and meta-analysis aimed to determine intraoperative noise levels worldwide. METHODS: Five databases were searched from inception to May 2026, in accordance with Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines. Studies were eligible for inclusion if they included surgical specialty and a measure of noise sampled recorded with validated sound metres. Studies were eligible for meta-analysis if they included a mean time-weighted average. Two authors undertook searches and risk-of-bias assessment. Meta-regression estimated pooled means, heterogeneity, and variance. RESULTS: Fifty studies met the inclusion criteria in the systematic review, with 28 studies providing 43 unique datasets subclassified by type of surgical procedure for analysis. The pooled random-effects mean intraoperative noise level was 70.7 A-weighted dB [dB(A)] (95% CI 69.0-72.3). Subgroup analysis demonstrated the highest exposures in otolaryngology at 78.8 dB(A) (95% CI 72.8-84.7) and orthopaedics at 73.3 dB(A) (95% CI 68.9-77.8).