anaesthetic drug
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Author(s):  
Nagalingeswaran Ahilasamy ◽  
Rajendran Dinesh Kumar ◽  
Hem Anand Nayagam ◽  
Omprakash Shanmuganandam ◽  
K. R. Vaibhavi ◽  
...  

2020 ◽  
Vol 45 (10) ◽  
pp. 1066-1070
Author(s):  
Panai Laohaprasitiporn ◽  
Yuwarat Monteerarat ◽  
Roongsak Limthongthang ◽  
Torpon Vathana ◽  
Vajara Wilairatana

We conducted a randomized controlled trial to compare pain scores and patient satisfaction between topical anaesthetic cream (5% lidocaine-prilocaine cream) versus placebo cream, applied approximately 90 minutes before local anaesthetic injection for open trigger digit release. One hundred participants were enrolled and randomly allocated into the two groups between May 2019 and February 2020. The visual analogue pain scores and satisfaction scores were measured. Most participants were female with Quinnell Grade 2–3 trigger digits. The pain scores during needle injection, local anaesthetic infiltration, the overall pain and satisfaction scores had no statistically significant differences between groups. There was no correlation between duration of topical anaesthetic drug application and pain scores. Subgroup analysis did not show significant differences in pain scores between genders. No complications were found during the study period. The topical anaesthetic drug was ineffective to use on the palmar skin during open trigger digit release surgery. Level of evidence: II


2020 ◽  
Vol 32 (9) ◽  
pp. 2180-2186
Author(s):  
S.P.N. SHARAVANAN ◽  
C.S. VENKATESAN ◽  
D. BHASKARA SURESH RAJU ◽  
S. KABILAN

A series of ropivacaine analogues were synthesized by altering the methyl group substituent in the aromatic ring. The synthesized compounds (2a-f and 3a-f) were characterized by using IR, NMR and HRMS analysis and then compounds 3a-3f were screened in vitro anticancer (MTT assay) activity against breast cancer cell line (MCF-7), antibacterial and antioxidant (DPPH scavenging assay) studies. The biological studies revealed that the compounds 3c and 3f have shown a good inhibitory activity against MCF-7 cell line. Compounds 3e, 3b, 3c and 3f showed moderate antioxidant activity. There was no inhibition observed against both Gram-positive and Gram-negative bacteria.


2019 ◽  
Vol 70 (5) ◽  
pp. 1888-1892
Author(s):  
Mary-Nicoleta Lupu ◽  
Magdalena Miulescu ◽  
Ioana Anca Stefanopol ◽  
Gabriela Stoleriu ◽  
Madalina Nicoleta Matei ◽  
...  

Sevoflurane (2,2,2-trifluoro-1-[trifluoromethyl]ethyl fluoromethyl ether or C4H3F7O), with a molar mass 200.055 g/mol, also called fluoromethyl, is a highly fluorinated methyl isopropyl ether with general anesthetic property, available for clinical practice for about 30 years. Sevoflurane is a sweet-smelling, non-flammable and it is used for induction and maintenance of general anesthesia. Together with desflurane, it is replacing isoflurane and halothane in modern anesthesiology. Propofol (2,6-diisopropylphenol or C12H18O), with a molar mass 178.271g/mol is an alkylphenol derivative formulated for induction and maintenance (in some cases) of general anesthesia, sedation and hypnosis and acting as an intravenous anaesthetic drug, having largely replaced sodium thiopental because recovery from propofol is more rapid and clear.


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