Δευτέρα 26 Νοεμβρίου 2018
From Total Volume to Sequence Maps—Sophisticated Accelerometer Data Analysis
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Grounded Running Reduces Musculoskeletal Loading
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Quantifying Brain White Matter Microstructure of People with Lateral Ankle Sprain
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Κυριακή 25 Νοεμβρίου 2018
Sedation and neurodevelopmental outcomes in PICU: identification of study groups
Abstract
Background/Aims
As little as 30 minutes of exposure to anesthetic and sedative agents may adversely affect the developing brain. Safe, humane management of critically ill infants requires the use of sedative agents, often for prolonged periods. We sought to identify two comparable groups of critical care patients who did or did not receive sedatives, with the aim of designing a long‐term neuro‐development follow‐up study. This feasibility study aimed to determine if two comparable groups could be found.
Methods
Infants with respiratory diagnoses having non‐invasive ventilation without sedation (Group C) or intubation and ventilation with sedation (Group S) were identified by chart review. Charts of patients fulfilling the above inclusion criteria were searched for exclusion criteria including neurological disease, extreme prematurity, congenital cardiac disease, genetic anomalies. Data was extracted to score pediatric severity of illness scores (PRISM and PELOD) for each patient. These scores were then compared using the absolute scores and by risk strata.
Results
Group S included 33 patients and Group C had 39. The absolute PRISM and PELOD scores were different between groups, Comparing the groups in 3 risk strata (PRISM greater or less than 5 or 10) there were no significant differences between groups
Conclusions
It is not possible to randomise infants to sedation or no sedation to investigate neurodevelopmental outcomes. This phase of the project aimed to determine the comparability of 2 groups of PICU patients.
These findings indicate that these groups could be enrolled as exposed and control subjects in an outcomes study.
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Physico‐chemical stability of Plasma‐Lyte 148 ® and Plasma‐Lyte 148 ® + 5% Glucose with eight common intravenous medications
Abstract
Background
Plasma‐Lyte 148 ® is a balanced, crystalloid intravenous (IV) fluid which is both calcium‐free and isotonic. It prevents the hyperchloraemic metabolic acidosis and iatrogenic hyponatraemia seen with use of 0.9% sodium chloride and hypotonic solutions respectively. However, data on compatibility with commonly used drugs is lacking.
Aim
To investigate the stability of Plasma‐Lyte 148 ® and Plasma‐Lyte 148 ® + 5% Glucose with eight commonly used therapeutic agents when compared with 5% Glucose and 0.9% Sodium Chloride as diluents. We aimed to provide vital data which may facilitate the introduction of what appears to be a safer and more economic fluid.
Method
Plasma‐Lyte 148 ® and Plasma‐Lyte 148 ® + 5% Glucose were mixed with morphine, midazolam, fentanyl, ketamine, clonidine, aminophylline, salbutamol and furosemide at set concentrations. Comparisons were made to 0.9% Sodium Chloride and 5% Glucose fluid controls. Six repeats of each IV fluid and drug admixture were analysed through high performance liquid chromatography (HPLC), at three time points: 0, 2 and 24 hours. A concentration change of < 5% was defined as chemically stable. Physical stability was assessed by observation of precipitate formation or colour change. pH changes were measured using a Fisherbrand Hydrus 300 pH meter.
Results
Relative to starting concentration, all drugs except midazolam were stable to +/‐ 3%. All examined therapeutic agents were chemically stable at 2 and 24 hours relative to control solutions. No precipitate formed in any of the samples. All Plasma‐Lyte 148 ® and Plasma‐Lyte 148 ® + 5% Glucose drug admixtures remained in a safe, peripheral administration pH range of 5‐9 and were closer to the pH of blood than standard fluid‐drug admixtures.
Conclusion
Morphine, fentanyl, ketamine, salbutamol, aminophylline, and clonidine are stable for 24 hours when mixed with Plasma‐Lyte 148 ® and Plasma‐Lyte 148 ®+5% Glucose for administration at concentrations equivalent to those found at a typical Y site with maintenance fluid. Furosemide is stable at lower concentrations than those seen at a Y‐site, but midazolam displayed instability.
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Sips for little lips‐ letter to the editor
Abstract
We write to you in relation to your recent important publication of the consensus statement on clear fluid fasting for elective paediatric general anaesthesia, that emphasises improving fasting times from two hours to one hour prior to surgery[1].
In order to determine the volume of clear fluid to be given, one of the practical interventions advised by the author was to use an age‐based banded calculator. This eliminates the need to weigh the child prior to fluid administration.
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A Follow‐up Survey of Total Intravenous Anesthesia Usage in Children in the U.K. and Ireland
Abstract
Background
Total intravenous anesthesia usage in children remains relatively unpopular in the UK and Ireland. A postal survey by Hill et al in 2008 indicated that only 26% of Consultants used a propofol infusion at least once a month.
Aim
Following an increase in teaching and training opportunities in pediatric total intravenous anesthesia in the UK, we repeated the survey amongst Consultant members of Association of Paediatric Anaesthetists of Great Britain and Ireland and Society for Intravenous Anaesthesia, to see if this had affected total intravenous anesthesia usage in children and how practice may have changed.
Methods
We used an anonymous online survey sent to APAGBI and SIVA members.
Results
A total of 291 responses were analysed. Total intravenous anesthesia was the default method of anesthesia in 8% of respondents and a further 46% used total intravenous anesthesia at least monthly. Overall total intravenous anesthesia usage had increased in the past year in 53%. The main indications were malignant hyperthermia susceptibility, and postoperative nausea and vomiting. ENT Surgery was the most popular surgical specialty. The main reasons for not using total intravenous anesthesia were that it was too 'fiddly' and lack of confidence in the user. Most respondents used propofol in combination with remifentanil. Over 80% used propofol target‐controlled infusion. The potential for propofol‐related infusion syndrome concerned many, with 74% limiting infusion duration as a result. Bispectral Index was not used routinely by the majority of anesthetists. Even though most anesthetists did not use total intravenous anesthesia routinely, 98% felt they would be confident to anesthetize an MH positive patient using the technique.
Conclusion
This survey has shown that although total intravenous anesthesia is not the default anesthetic technique for most anesthetists, overall usage in children has more than doubled in the past 10 years, with many happy to use it in a wide variety of patients and procedures.
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