Daily ReportOct 16, 2026
Anesthesiology, October 16 edition
We read 45 papers and selected 3.
Summary
Today’s strongest anesthesiology evidence includes a randomized noninferiority trial supporting phrenic nerve-sparing shoulder field anesthesia, a meta-analysis suggesting—but not yet confirming—perioperative ketamine or esketamine for postoperative delirium prevention, and a randomized trial showing that laparoscopic-guided transversus abdominis plane block strategies improve early analgesia after laparoscopic cholecystectomy. Collectively, these studies emphasize individualized regional anesthesia, cautious interpretation of emerging pharmacologic evidence, and multimodal opioid-sparing perioperative care.
Research Themes
- Phrenic nerve-sparing regional anesthesia
- Pharmacologic prevention of postoperative delirium
- Multimodal and opioid-sparing postoperative analgesia
Selected Articles
1. Comparison of Shoulder Field Anesthesia (SFA) with Interscalene Block (ISB) for Analgesia After Arthroscopic Shoulder Surgery: A Randomized Noninferiority Trial.
In this randomized trial of 80 patients, surgeon-performed shoulder field anesthesia was noninferior to interscalene block for cumulative 48-hour postoperative pain. Interscalene block provided better analgesia at 4–8 hours, but shoulder field anesthesia had similar opioid use and satisfaction, shorter hospital stay, and no observed Horner syndrome or respiratory events.
Impact: This study provides clinically relevant Level I evidence for a lung-sparing alternative to interscalene block, directly addressing a major safety limitation of a standard shoulder analgesic technique. Its noninferiority design supports individualized selection of regional anesthesia according to respiratory risk.
Clinical Implications: Shoulder field anesthesia can be considered when avoiding phrenic nerve dysfunction is important, particularly in patients with limited pulmonary reserve or elevated risk from hemidiaphragmatic paralysis. Clinicians should recognize that interscalene block may provide superior analgesia during the first several postoperative hours.
Key Findings
- Shoulder field anesthesia was noninferior to interscalene block for cumulative 48-hour pain, with a mean difference of -0.824 NRS points for ISB minus SFA and a 95% confidence interval of -1.853 to 0.206.
- Interscalene block produced lower pain scores at 4–8 hours, but cumulative opioid consumption and patient satisfaction were similar.
- Horner syndrome occurred in 2 patients and a respiratory event requiring intensive care occurred in 1 patient in the interscalene group; none occurred in the shoulder field anesthesia group.
Methodological Strengths
- Randomized noninferiority design with a prespecified cumulative 48-hour pain endpoint and noninferiority margin.
- Assessment included pain, opioid consumption, satisfaction, hospital stay, and clinically important block-related complications.
Limitations
- Only 80 patients completed the study, limiting precision for uncommon complications.
- All participants were White and 80% were of Middle Eastern ethnicity, which limits generalizability to other populations.
- The trial was not described as blinded, and early postoperative analgesia favored interscalene block.
Future Directions: Larger, multicenter trials should confirm respiratory safety using systematic diaphragmatic ultrasound and pulmonary function testing, and should evaluate procedure-specific outcomes across diverse populations and surgical settings.
BACKGROUND: An interscalene brachial plexus block (ISB) is commonly used for analgesia after shoulder surgery but is associated with neurologic and respiratory complications, including hemidiaphragmatic paralysis. Surgeon-performed shoulder field anesthesia (SFA) is a landmark-guided, phrenic nerve-sparing technique that may provide effective analgesia with fewer complications. The purpose of this study was to compare SFA with ISB for pain control after arthroscopic shoulder surgery.
2. Effects of Ketamine and Esketamine on Postoperative Delirium After General Anesthesia: A Meta-Analysis and Meta-Regression Analysis.
This meta-analysis included 25 randomized controlled trials involving 3344 patients. Ketamine and esketamine were associated with lower postoperative delirium risk, particularly with higher-dose or bolus-plus-infusion regimens and in major surgery, but trial sequential analysis indicated that the cumulative evidence remains inconclusive; dizziness was increased.
Impact: The study synthesizes the largest evidence base in the provided set for a clinically important and unresolved perioperative question. Its explicit dose-response exploration and trial sequential analysis appropriately temper enthusiasm and argue against routine adoption before adequately powered multicenter trials.
Clinical Implications: Ketamine or esketamine may be considered investigational options for selected high-risk patients, especially during major surgery, but the current evidence does not support routine prophylactic use. Clinicians should weigh possible delirium benefit against increased dizziness and the uncertainty of the evidence.
Key Findings
- Twenty-five randomized controlled trials involving 3344 patients were included.
- Ketamine reduced postoperative delirium risk versus control with RR 0.69, while esketamine reduced risk with RR 0.58.
- Benefits were more evident with higher-dose regimens, bolus-plus-infusion administration, major surgery, and assessment 2–7 days after surgery; dizziness increased with RR 1.45.
- Trial sequential analysis indicated that the evidence remains inconclusive because the required information size has not been reached.
Methodological Strengths
- Systematic search of PubMed, Embase, and CENTRAL with restriction to randomized controlled trials.
- Use of subgroup analyses, meta-regression, sensitivity analyses, and trial sequential analysis to examine robustness and clinical heterogeneity.
Limitations
- Trial sequential analysis showed insufficient information size, so the apparent benefit may change with future trials.
- Dosing, surgical populations, delirium assessment methods, and comparators varied across the included studies.
- The reduction in postoperative depressive symptoms was based on only 2 studies involving 493 patients.
Future Directions: Large, multicenter, prospectively registered randomized trials should standardize delirium definitions, timing of assessment, dosing strategies, active comparators, and adverse-event reporting, with particular attention to older adults undergoing major surgery.
BACKGROUND: Postoperative delirium (POD) is a frequent and serious complication, particularly in older adults undergoing major surgery. Pharmacologic prevention remains limited. This study aimed to evaluate whether perioperative ketamine or esketamine reduces POD incidence and to explore optimal administration strategies. METHODS: We systematically searched PubMed, Embase, and Cochrane Central Register of Controlled Trials (CENTRAL) from inception to January 2025 for randomized controlled trials (RCTs) comparing perioperative ketamine or esketamine with placebo or standard care.
3. Laparoscopic-guided transversus abdominis plane block with low-pressure versus standard-pressure pneumoperitoneum versus port site infiltration with standard-pressure pneumoperitoneum for postoperative pain management in laparoscopic cholecystectomy: randomized controlled trial.
In this prospective open-label randomized trial of 180 patients, both TAP block strategies reduced early postoperative pain and rescue tramadol use compared with port-site infiltration. The combination of low-pressure pneumoperitoneum and laparoscopic-guided TAP block produced lower coughing and resting pain at 6 hours and less shoulder-tip pain, although differences in local anesthetic dose, volume, and timing limit attribution to individual components.
Impact: The study tests a pragmatic, readily implementable combination of regional anesthesia and surgical technique that may improve recovery while reducing opioid rescue medication. Its value is primarily clinical and operational, although the multifactorial intervention limits mechanistic attribution.
Clinical Implications: TAP block may be preferred over port-site infiltration when reducing early pain and rescue opioid use is a priority after laparoscopic cholecystectomy. Low-pressure pneumoperitoneum may offer additional benefit, but the choice should consider surgical exposure and the lack of component-specific attribution.
Key Findings
- One hundred eighty patients were randomized equally to L-TAP, S-TAP, or S-PS groups.
- Rescue tramadol use was 8.3% with L-TAP, 13.3% with S-TAP, and 41.7% with S-PS.
- At 6 hours, L-TAP produced lower pain during coughing and while lying than S-TAP, with p = 0.009 for both comparisons.
- Shoulder-tip pain was lower with L-TAP than S-PS, occurring in 3.3% versus 20.0% of patients; day-1 discharge rates were 96.7%, 95.0%, and 86.7%, respectively.
Methodological Strengths
- Prospective three-arm randomized controlled design with predefined analgesic strategies and multiple recovery outcomes.
- Assessment included pain in several positions and time points, rescue analgesia, shoulder-tip pain, mobility, postoperative nausea and vomiting, and discharge timing.
Limitations
- The trial was open-label, allowing performance and assessment bias.
- No single timepoint-position combination was designated as a standalone primary endpoint, creating a multiple-comparisons concern.
- Local anesthetic dose, volume, and timing differed between groups, preventing isolation of the effects of low-pressure pneumoperitoneum and TAP block.
Future Directions: Future trials should use factorial or otherwise component-controlled designs with standardized local anesthetic dosing, a prespecified primary endpoint, blinded outcome assessment where feasible, and patient-centered recovery outcomes such as quality of recovery and opioid-related adverse effects.
BACKGROUND: Postoperative pain remains a significant challenge following laparoscopic cholecystectomy, influencing recovery, opioid consumption, and hospital stay. Laparoscopic-guided transversus abdominis plane (TAP) block and low-pressure pneumoperitoneum have independently demonstrated analgesic benefits. This study compared three predefined perioperative analgesic strategies: low-pressure pneumoperitoneum with laparoscopic-guided TAP block (L-TAP), standard-pressure pneumoperitoneum with TAP block (S-TAP), and standard-pressure pneumoperitoneum with port-site infiltration (S-PS). METHODS: A prospective, open-label, three-arm randomized controlled trial was conducted at a tertiary care center.