Anesthesia and analgesia
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Anesthesia and analgesia · Nov 2013
The Cost of Resident Scholarly Activity and Its Effect on Resident Clinical Experience.
Scholarly activity is an important aspect of the academic training of future anesthesiologists. However, residents' scholarly activity may reduce training caseloads and increase departmental costs. ⋯ Residents' scholarly activities require significant departmental financial support. Residents who elected to spend months conducting research completed significantly more scholarly projects but experienced fewer clinical cases.
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Anesthesia and analgesia · Nov 2013
The Effect of Endoplasmic Reticulum Stress on Neurotoxicity Caused by Inhaled Anesthetics.
The mechanisms by which inhaled anesthetics cause neurotoxicity are not well clarified. Exposure to inhaled anesthetics induces a release of Ca from the endoplasmic reticulum (ER) into the cytosol. Aberrant Ca mobilization may alter the protein-folding environment in the ER, causing ER stress. Binding immunoglobulin protein (BiP) is an ER chaperone that is critical to ER functions. Because ER stress leads to cellular dysfunction and apoptotic cell death, leading to diverse human disorders such as neurodegenerative diseases, we hypothesized ER stress may play a role in neurotoxicity caused by inhaled anesthetics. ⋯ Sevoflurane exposure may cause ER stress, which is tolerated to some extent in wild-type cells. When this tolerance is limited, like in cells with mutant BiP, the exposure leads to cell death in the brain, suggesting that ER stress may partially mediate neurotoxicity caused by inhaled anesthetics. This study suggests that patients with certain conditions sensitive to ER stress such as ischemia, hypoxia, developing brain, or neurodegenerative diseases may be vulnerable to inhaled anesthetics.
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Anesthesia and analgesia · Nov 2013
Automated, Real-Time Fresh Gas Flow Recommendations Alter Isoflurane Consumption During the Maintenance Phase of Anesthesia in a Simulator-Based Study.
The Low Flow Wizard (LFW) provides real-time guidance for user optimization of fresh gas flow (FGF) settings during general inhaled anesthesia. The LFW can continuously inform users whether it determines their FGF to be too little, efficient, or too much, and its color-coded recommendations respond in real time to changes in FGF performed by users. Our study objective was to determine whether the LFW feature, as implemented in the Dräger Apollo workstation, alters FGF selection and thereby volatile anesthetic consumption without affecting patient care. ⋯ Our data in a simulated anesthetic suggest that enabling the display of FGF efficiency data by the LFW results in a median percent reduction in volatile liquid anesthetic consumption rate of 53.2%. Since the lower limit of the 95% confidence interval for the median is 39.4%, this finding is likely to translate into cost savings and less waste anesthetic gas generated in the clinical setting and released into the atmosphere.
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Anesthesia and analgesia · Nov 2013
The Distinct Effects of Lipid Emulsions Used for "Lipid Resuscitation" on Gating and Bupivacaine-Induced Inhibition of the Cardiac Sodium Channel Nav1.5.
Systemic administration of lipid emulsions is an established treatment for local anesthetic intoxication. However, it is unclear by which mechanisms lipids achieve this function. The high cardiac toxicity of the lipophilic local anesthetic bupivacaine probably results from a long-lasting inhibition of the cardiac Na channel Nav1.5. In this study, we sought to determine whether lipid emulsions functionally interact with Nav1.5 or counteract inhibition by bupivacaine. ⋯ Our data indicate that lipid emulsions reduce rather than increase availability of Nav1.5. However, both Intralipid and Lipofundin partly relieve Nav1.5 from block by bupivacaine. These effects are likely to involve not only a direct interaction of lipids with Nav1.5 but also the ability of lipid emulsions to absorb bupivacaine and thus reduce its effective concentration.
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Anesthesia and analgesia · Nov 2013
Prevention of Airway Fires: Do Not Overlook the Expired Oxygen Concentration.
It is generally accepted that when an ignition source is used the inspired oxygen concentration (FIO2) should be <30% in the breathing circuit to help prevent airway fires. The time and conditions required to reduce a high O2% in the breathing circuit to <30% has not yet been systematically studied. ⋯ Both inspired and expired circuit oxygen concentration may take minutes to decrease to <30% depending on circuit length, FGF rate, and starting circuit oxygen concentration. During the reduction in FIO2, the expiratory oxygen concentration may be >30% for a considerable time after the FIO2 is in a "safe" range. An increased expired oxygen concentration should also be considered an airway fire risk, and patient care protocols may need to be modified based on future studies.