98%
921
2 minutes
20
Background: Remimazolam tosilate (RT) is a newly listed benzodiazepine for sedation and anesthesia featuring quick onset of effects, short maintenance and recovery times, which is currently under research. This trial was conducted to determine the median effective dose (ED) and the 95% effective dose (ED) of single-dose remimazolam for moderate sedation in elderly patients undergoing transurethral resection of the prostate (TURP) under spinal anesthesia, and to evaluate its efficacy and safety.
Methods: Thirty male patients aged 65-80 years old were recruited for selective TURP. Remimazolam was administered intravenously to pain-free patients (VAS score < 1) within 1 min of successful spinal anesthesia by the same anesthesiologist. We used modified Dixon's up-and-down sequential allocation method to determine the ED and ED of the agent with an initial dosage of 0.1 mg/kg. Successful sedation was defined as an MOAA/S score ≤ 3 and above 1. A score of > 3 was deemed as failed sedation. Recruitment continued until ten independent pairs (from successful sedation to failed sedation) would give a reliable estimation of the ED and ED of RT and their 95% confidence intervals.
Results: The ED of remimazolam was 0.063 (95% C.I. 0.045-0.073) mg/kg. Its ED was 0.079 (95% C.I. 0.07-0.137) mg/kg. Remimazolam was safe in its application.
Conclusions: A single-dose of RT proves to be safe for assisted sedation during TURP in elderly male patients under spinal anesthesia with a lower incidence of adverse events. Its ED and ED were 0.063 mg/kg and 0.079 mg/kg, respectively.
Trial Registration: http://www.chictr.org.cn (ChiCTR2100051912).
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9351252 | PMC |
http://dx.doi.org/10.1186/s12871-022-01788-1 | DOI Listing |
Heart Rhythm O2
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Division of Cardiology, Arrhythmia Section, Zentralklinik Bad Berka, Germany.
Background: Damage to peri-esophageal tissue may occur following pulmonary vein isolation (PVI). Active esophageal cooling has been shown to reduce the incidence of mucosal esophageal injury, probably by dissipation of heat and inhibition of inflammation. Whether it also protects the peri-esophageal vagal nerve plexus and reduces gastric hypomotility and food retention is uncertain.
View Article and Find Full Text PDFUlus Travma Acil Cerrahi Derg
September 2025
Department of Emergency, University of Health Science, Konya City Hospital, Konya-Türkiye.
Background: This study aimed to compare the effects of hematoma block (HB) and dexmedetomidine administration on pain control, reduction quality, and physician satisfaction during the reduction of distal radius fractures (DRFs) in the emergency department (ED).
Methods: A total of 60 patients presenting to the ED with DRFs were enrolled. Patients were randomly assigned to two groups: one received HB, while the other underwent conscious sedation with dexmedetomidine.
Naunyn Schmiedebergs Arch Pharmacol
September 2025
Medical Research Group of Egypt, Negida Academy, Arlington, MA, USA.
Upper gastrointestinal endoscopy (GIE) is essential for diagnosing and treating gastrointestinal disorders in children aged 6-12 years, yet it often requires sedation due to the significant discomfort and pain involved. We conducted a PRISMA 2020-compliant systematic review of randomized controlled trials (RCTs) from PubMed, Web of Science, Scopus, and Ovid (inception to March 30, 2024). Inclusion criteria are as follows: RCTs comparing sedative regimens (e.
View Article and Find Full Text PDFJ Bronchology Interv Pulmonol
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Department of Pulmonary and Critical Care Medicine, Hunan Provincial People's Hospital, The First Affiliated Hospital of Hunan Normal University, Changsha, Hunan, P.R. China.
Background: Transbronchial cryobiopsy (TBCB) is generally recommended under intubation or rigid bronchoscopy with general anesthesia. However, some patients with diffuse parenchymal lung disease (DPLD) are unable to tolerate general anesthesia, which limits the widespread adoption of TBCB.
Methods: A total of 37 patients with DPLD who underwent TBCB under conscious sedation without intubation were included in this study.
Struct Heart
August 2025
Pauley Heart Center, Virginia Commonwealth University Health, Richmond, Virginia.
Background: Since Food and Drug Administration approval of transcatheter aortic valve replacement (TAVR) in 2011, advancements in technology and procedural refinements have improved efficiency and safety. By systematically eliminating steps in the original TAVR protocol, we achieved reductions in procedural time, contrast volume, and fluoroscopy time without compromising outcomes.
Methods: Institutional TAVR data (November 2012 to September 2023) were analyzed, focusing on procedural times, contrast volume, radiation exposure, and outcomes.