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Instructions for Anesthesiology Programs Requesting the Addition of a Clinical Base Year (CBY) to an Existing 3-Year Accredited Residency
Instructions for Anesthesiology Programs Requesting the Addition of a Clinical Base Year (CBY) to an Existing 3-year Accredited Residency MATERIALS TO BE SUBMITTED: Attachment A: Clinical Base Year Information Form Attachment B: Provide specific goals and objectives (competency-based terminology) for each block rotation and indicate assessment tools that will be utilized. Attachment C: Include a description of both clinical and didactic experiences that will be provided (lectures, conferences, grand rounds, journal clubs). Attachment D: Provide an explanation of how residents will evaluate these experiences as well as supervising faculty members. Attachment E: Provide a one-page CV for the key supervising faculty. Attachment F: Clarify the role of the resident during each of the program components listed. Information about Anesthesiology Clinical Base Year ACGME RRC Program Requirements 7/08 1) Definition of Clinical Base Year (CBY) a) 12 months of ‘broad education in medical disciplines relevant to the practice of anesthesiology’ b) capability to provide the Clinical Base Year within the same institution is desirable but not required for accreditation. 2) Timing of CBY a) usually precedes training in clinical anesthesia b) strongly recommended that the CBY be completed before the resident begins the CA-2 year c) must be completed before the resident begins the CA-3 year 3) Routes of entry into Anesthesiology program a) Categorical program - Resident matches into categorical program (includes CB year, approved by RRC as part of the accredited -
Components of Respiratory Depression After Narcotic Premedication in Adolescents
COMPONENTS OF RESPIRATORY DEPRESSION AFTER NARCOTIC PREMEDICATION IN ADOLESCENTS R. KNILL*, J.F. Coscnowr P. M. OLLEY,AND H. LEVISON N~d~COTIC ACENTS are potent depressants of ventilation. 1-5 Although this effect is generally assumed to result from decreased output of the central respiratory "'centres," some of the effect could be due to direct action on the ventilatory apparatus itself, by increasing respiratory impendance. For example, both morphine and meperidine can cause bronchoconstriction;" furthermore they can increase the tonic activity of abdominal and intercostal muscles, r-l~ The mechanical effects of this increase in abdominal wall tone have not been assessed after thera- peutic doses of these agents, but large doses of narcotics administered intravenously produce board-like rigidity of the abdominal wall r-lo and markedly decrease total respiratory compliance? As the magnitude of this effect appears to be dose related 1~ it may well be present to a lesser extent after therapeutic doses of these agents. The purpose of this work was to determine whether the ventilatory depression associated with morphine and a meperidine-phenothiazine mixture is solely the result of impairment of the neuromuscular or force-generating mechanisms, or is in part due to increased impedance of the ventilatory pump. Even small increases in ventilatory load with narcotics probably contribute to ventilatory depression, as load compensation is poor when central neural mechanisms are pharmacologi- cally imp aired. 11,1a The conventional technique for examining the effect of narcotics on ventilation is to apply rebreathing and steady-state.methods before and after medication, to measure changes in minute ventilation (V~) and tidal volume (VT).13,~4 However, these measurements depend on both central output and the properties of the ventilatory apparatus, ~,16 without distinction between them. -
Powering Your Performance
POWERING YOUR PERFORMANCE B105M | B125M | B155M Modular Patient Monitors gehealthcare.com Advanced capabilities. Simple scalability. Dependable technology. B1x5M range of modular patient monitors deliver premium clinical performance across care areas. Scalable platform You can monitor essential vital signs (ECG, SpO2, Temp, NIBP, RR) and easily scale to advanced parameter modules like respiratory gases and Clinical precision anesthetic agents, NMT and Entropy™ – up to three advanced parameters simultaneously. These accurate, reliable, and easy-to-use monitors Intuitive design enable simple and intuitive workflow with a choice of 10-, 12- or 15-inch touch screen displays. B1x5M range of monitors come with Value Dependable technology Software Platform (VSP 3.0). Legacy of premium clinical performance. Excellence of advanced features. Timely clinical decisions. GE Healthcare’s more than 45 years of clinical excellence in The B1x5M range of modular patient monitors helps you quickly designing reliable patient monitoring systems provides you with take charge of patient conditions like arrhythmia and high/low advanced features, such as: blood pressure, and efficiently assess the level of consciousness. They seamlessly integrate with the CARESCAPE Ecosystem for centralized alarm management and efficient workflow. • DINAMAP™ SuperSTAT™ NIBP • EK-Pro v14 algorithm The solutions allow you to effectively monitor deteriorating • CO sidestream and cardiac output patient conditions and make timely interventions by tracking the 2 National Early Warning -
Analgesia and Sedation in Hospitalized Children
Analgesia and Sedation in Hospitalized Children By Elizabeth J. Beckman, Pharm.D., BCPS, BCCCP, BCPPS Reviewed by Julie Pingel, Pharm.D., BCPPS; and Brent A. Hall, Pharm.D., BCPPS LEARNING OBJECTIVES 1. Evaluate analgesics and sedative agents on the basis of drug mechanism of action, pharmacokinetic principles, adverse drug reactions, and administration considerations. 2. Design an evidence-based analgesic and/or sedative treatment and monitoring plan for the hospitalized child who is postoperative, acutely ill, or in need of prolonged sedation. 3. Design an analgesic and sedation treatment and monitoring plan to minimize hyperalgesia and delirium and optimize neurodevelopmental outcomes in children. INTRODUCTION ABBREVIATIONS IN THIS CHAPTER Pain, anxiety, fear, distress, and agitation are often experienced by GABA γ-Aminobutyric acid children undergoing medical treatment. Contributory factors may ICP Intracranial pressure include separation from parents, unfamiliar surroundings, sleep dis- PAD Pain, agitation, and delirium turbance, and invasive procedures. Children receive analgesia and PCA Patient-controlled analgesia sedatives to promote comfort, create a safe environment for patient PICU Pediatric ICU and caregiver, and increase patient tolerance to medical interven- PRIS Propofol-related infusion tions such as intravenous access placement or synchrony with syndrome mechanical ventilation. However, using these agents is not without Table of other common abbreviations. risk. Many of the agents used for analgesia and sedation are con- sidered high alert by the Institute for Safe Medication Practices because of their potential to cause significant patient harm, given their adverse effects and the development of tolerance, dependence, and withdrawal symptoms. Added layers of complexity include the ontogeny of the pediatric patient, ongoing disease processes, and presence of organ failure, which may alter the pharmacokinetics and pharmacodynamics of these medications. -
Journal Watch 1805 TCCC.Pdf
TCCC Journal Watch May 2018 Abou El Fadl M, O’Phelan K: Management of traumatic brain injury: an update. Neurosurg Clin N Am 2018;29:213-221 Abraham P,Russell D, Huffman S, et al: Army combat medic resilience: the process of forging loyalty. Mil Med 2018;183:364-370 Adravanti P, Di Salvo E, Calafiore G, et al: A prospective, randomized, comparative study of intravenous alone and combine intravenous and intraarticular administration of tranexamic acid in primary total knee replacement. Arthoplast Today 2017;4:85-88 Aggarwal N, Brower R, Hager D, et al: Oxygen exposure resulting in arterial oxygen tensions above the protocol goal was associated with worse clinical outcomes in acute respiratory distress syndrome. Crit Care Med 2018;46:517-524 Agimi Y, Regasa L, Ivins B, et al: Role of Department of Defense policies in identifying traumatic brain injuries among deployed US Service members 2001- 2016. Aiolfi A, Benjamin E, Recinos G, et al: Air versus ground transportation in isolated severe head trauma: a national trauma bank study. J Emerg Med 2018;54:328- 334 Aji Y, Apriawan T, Bajamal A: Traumatic supra- and infra-tentorial extradural hematoma: case series and literature review. Asian J Neurosurg 2018;13:453- 457 Akbari E, Safari S, Hatamabadi H: The effect of fibrinogen concentrate and fresh frozen plasma on the outcome of patients with acute traumatic coagulopathy: a quasi-experimental study. Am J Emerg Med 2018;Epub ahead of print. Aries M, Donnelly J: Brain oxygenation optimization after severe traumatic brain injury: an ode to preventing brain hypoxia. Crit Care Med 2018;46:e350 Armstrong R: Visual problems associated with traumatic brain injury. -
Pharmacy Phacts in This Issue Pharmd Candidates Discuss Oral Health and Preventing Eye Strain at Work
Pharmacy Phacts In this issue PharmD candidates discuss Oral Health and Preventing Eye Strain At Work Oral Health Landon Forrest Stewart, PharmD Candidate 2021 Why is Oral Health important? Oral health is an important part of our overall health. Oral health issues can cause oral pain, increased costs in healthcare, and less productivity. Recent developments in oral hygiene have led to improved outcomes for patients. Many oral health issues are still prevalent today, but the good news is that many are preventable with daily healthy habits. Healthy habits are required to maintain good oral health and many oral health issues are still prevalent today. One of the most common oral health problems is decay in the tooth also known as a cavity. The outer layer of the tooth is a tough mineral layer called the enamel. Bacteria group together on teeth to form plaques that can erode the enamel and the deeper layers of your teeth, causing cavities. Cavities are present and untreated in up to 26% up American adults. (1) If left untreated, they can lead to pain in the tooth and more severe infections known as an abscess. Another common oral health problem is gum disease. When bacteria group together on the teeth, it causes the immune system to respond and causes inflammation in the mouth. The initial inflammation is called gingivitis and makes your gums swell and bleed more easily. Untreated gingivitis can progress to a more severe gum disease called periodontitis. Periodontitis can damage the structure that holds your teeth in place and is a common cause of tooth loss. -
General Anaesthesia in Oral Surgery and Outpatient Surgery History
Department of Oral- and Maxillofacial Surgery, Semmelweis University Budapest Head of Department: Dr. Németh Zsolt General anaesthesia in oral surgery and outpatient surgery History 1844 Horace Wells nitrous oxide extraction of one of his own wisdom teeth by a colleague 1846 William Morton (pupil of Wells) ether extraction 1946 introduction of lidocaine General anaesthesia should be strictly limited to those patients and clinical situations in which local anaesthesia (with or without sedation) is not an option. Bourne JG. General anaesthesia in the dental surgery. B Dental J 1962; 113: 54-7. Coleman F. The history of nitrous oxide anaesthesia. Dental Record 1942; 62: 143-9 Naveen Malhotra General Anaesthesia for Dentistry ndian Journal of Anaesthesia 2008;52:Suppl (5):725-737 Types of general anaesthesia Outpatient anaesthesia • Dental chair anaesthesia Relative analgesia for simple extraction • Day care anaesthesia Conscious sedation (Sedoanalgesia) for minor oral surgery In patient anaesthesia Intubation with or without neuromuscular blocking for complicated extractions, oral- and maxillofacial surgical procedures Indications of general anaesthesia • Acute infection (pain) • Children • Mentally challenged patients • Dental phobia • Allergy to local anaesthetics • Extensive dentistry & facio-maxillary surgery Equipments • anaesthesia machine, vaporizers • oxygen, nitrous oxide • breathing circuits (adult and pediatric) • nasal and facial masks • oral and nasal air-ways • different laryngoscopes with all sizes of blades • nasal and -
Methohexital(BAN, Rinn)
1788 General Anaesthetics metabolic pathways include hydroxylation of the 3. Lökken P, et al. Conscious sedation by rectal administration of Methohexital Sodium (BANM, rINNM) midazolam or midazolam plus ketamine as alternatives to gener- cyclohexone ring and conjugation with glucuronic ac- al anesthesia for dental treatment of uncooperative children. Compound 25398; Enallynymalnatrium; Méthohexital Sodique; id. The beta phase half-life is about 2.5 hours. Keta- Scand J Dent Res 1994; 102: 274–80. Methohexitone Sodium; Metohexital sódico; Natrii Methohexi- 4. Louon A, et al. Sedation with nasal ketamine and midazolam for talum. mine is excreted mainly in the urine as metabolites. It cryotherapy in retinopathy of prematurity. Br J Ophthalmol crosses the placenta. 1993; 77: 529–30. Натрий Метогекситал 5. Zsigmond EK, et al. A new route, jet-injection for anesthetic in- C14H17N2NaO3 = 284.3. ◊ References. duction in children–ketamine dose-range finding studies. Int J CAS — 309-36-4; 22151-68-4; 60634-69-7. 1. Clements JA, Nimmo WS. Pharmacokinetics and analgesic ef- Clin Pharmacol Ther 1996; 34: 84–8. ATC — N01AF01; N05CA15. fect of ketamine in man. Br J Anaesth 1981; 53: 27–30. 6. Kronenberg RH. Ketamine as an analgesic: parenteral, oral, rec- tal, subcutaneous, transdermal and intranasal administration. J ATC Vet — QN01AF01; QN05CA15. 2. Grant IS, et al. Pharmacokinetics and analgesic effects of IM and Pain Palliat Care Pharmacother 2002; 16: 27–35. oral ketamine. Br J Anaesth 1981; 53: 805–9. Pharmacopoeias. US includes Methohexital Sodium for In- jection. 3. Grant IS, et al. Ketamine disposition in children and adults. Br J Nonketotic hyperglycinaemia. -
Local Anaesthesia for Major General Surgical Postgrad Med J: First Published As 10.1136/Pgmj.72.844.105 on 1 February 1996
Postgrad Med J' 1996; 72: 105-108 C) The Fellowship of Postgraduate Medicine, 1996 Local anaesthesia for major general surgical Postgrad Med J: first published as 10.1136/pgmj.72.844.105 on 1 February 1996. Downloaded from procedures A review of 1 16 cases over 12 years A Dennison, N Oakley, D Appleton, J Paraskevopoulos, D Kerrigan, J Cole, WEG Thomas Summary ation was collated from medical notes, anaes- Between 1980 and 1992, 116 patients had thetic records and operation notes. Cases in either a simple mastectomy (32) or intra- which local anaesthesia was augmented by abdominal procedures (84) under local regional or intravenous techniques were exc- anaesthesia (0.5-1% lignocaine with luded from the study. Patients were not 1:200 000 adrenaline). A wide variety of included ifthey had neck/head or limb surgery, general surgical procedures were feasible abdominal hernia repair, simple drainage of using only supplementary intravenous intra-abdominal abscess or any minor proce- sedation (54%). Complications were un- dures including peritoneo-venous shunts, common and related to surgical proce- laparoscopic or endoscopic procedures. dure (three incorrect diagnoses, three The 116 patients presented in the study are procedures impossible) rather than the those who had intra-abdominal surgery (84; 53 anaesthetic technique. There were no women, 31 men) or simple mastectomy (32). anaesthetic toxicity or postoperative pro- The median age was 74 years (range 27-92) blems. Local anaesthesia is extremely and all the patients were grade III or worse on safe and facilitates larger surgical proce- the American Society of Anaesthesiologists dures than is generally appreciated. -
Study Protocol
RESEARCH PROTOCOL Project Title A multicenter, single blind, randomized controlled trial of virucidal effect of Polyvinylpyrrolidone-Iodine on SARS-CoV-2 as well as safety of its application on nasopharynx & oropharynx of COVID-19 positive patients BMRC Reg. No: 38624012021 Page-1/17 Project Title A multicenter, single blind, randomized controlled trial of virucidal effect of Polyvinylpyrrolidone- Iodine on SARS-CoV-2 as well as safety of its application on nasopharynx & oropharynx of COVID- 19 positive patients. Summary Povidone Iodine (Iodine with water soluble polymer Polyvinylpyrolidone) or PVP-I is a proven and time trusted antiseptic agent having best possible (99.99%) virucidal effect in it‟s only 0.23% concentration, against all viruses including SARS-Co, MERS-CoV; even in SARS-COV-2 due to it‟s nonspecific mode of action for virus killing and having no resistance [1,2]. Corona virus is transmitted by/via respiratory droplets or aerosol, produced from sneezing or coughing of infected persons to healthy individual through mouth and nose mainly [5, 6]. The routes of entry of coronavirus in human body are mouth, nose and eye. PVP-I products for gargling the throat and spraying or washing the nose may have a preventive effect on COVID-19 and if it is proved in this study following human trial, this will be a landmark research in COVID-19 pandemic. In line of this, PVP-I containing oro-nasal spray, proposed Bangasafe, which should be regarded as PONS (Povidone Iodine oro-nasal spray) in this protocol, has been developed and proposed to use against corona virus disease. -
Jebmh.Com Original Research Article
Jebmh.com Original Research Article A COMPARATIVE STUDY OF SMALL DOSE OF KETAMINE, MIDAZOLAM AND PROPOFOL AS COINDUCTION AGENT TO PROPOFOL Abhimanyu Kalita1, Abu Lais Mustaq Ahmed2 1Senior Resident, Department of Anaesthesiology, Assam Medical College, Dibrugarh. 2Associate Professor, Department of Anaesthesiology, Assam Medical College, Dibrugarh. ABSTRACT BACKGROUND The technique of “coinduction”, i.e. use of a small dose of sedative agent or another anaesthetic agent reduces the dose requirement as well as adverse effects of the main inducing agent. Ketamine, midazolam and propofol have been used as coinduction agents with propofol. MATERIALS AND METHODS This prospective, randomised clinical study compared to three methods of coinduction. One group received ketamine, one group received midazolam and one group received propofol as coinducing agent with propofol. RESULTS The study showed that the group receiving ketamine as coinduction agent required least amount of propofol for induction and was also associated with lesser side effects. CONCLUSION Use of ketamine as coinduction agent leads to maximum reduction of induction dose of propofol and also lesser side effects as compared to propofol and midazolam. KEYWORDS Coinduction, Propofol, Midazolam, Ketamine. HOW TO CITE THIS ARTICLE: Kalita A, Ahmed ALM. A comparative study of small dose of ketamine, midazolam and propofol as coinduction agent to propofol. J. Evid. Based Med. Healthc. 2017; 4(64), 3820-3825. DOI: 10.18410/jebmh/2017/763 BACKGROUND But, the major disadvantage of propofol induction are Propofol is the most frequently used IV anaesthetic agent impaired cardiovascular and respiratory function, which may used today with a desirable anaesthetic profile. It provides put the patients at a higher risk of bradycardia, hypotension faster onset of action, antiemesis, rapid recovery with and apnoea. -
Using Entropy in the General Anesthesia Managements
Research Article Clinics in Surgery Published: 07 Jul, 2017 Using Entropy in the General Anesthesia Managements Elif Büyükerkmen, Remziye Gül Sivaci and Elif Doğan Baki* Departement of Anesthesiology and Reanimation, Afyon Kocatepe University, Afyonkarahisar, Turkey Abstract Purpose: We aimed to investigate the effects of three general anesthesic management on depth of anesthesia, anesthesic quality, agent consumption and postoperative recovery. Materials and Methods: 90 patients scheduled for elective tympanoplasty and septoplasty surgery with American Society of Anesthesiologist (ASA) pysical status between I-III were included in this study. Neuromuscular transmission (NMT), surgical pleth index (SPI) and entropy were monitorized in addition to standart monitoring. Entropy was recorded as state entropy (SE) and response entropy (RE). After standart anesthesia induction, patients were divided into three groups according to maintenance of anesthesia using a sealed envelope system. Propofol 3-5 mg/kg/h iv infusion was performed to Group 1 (Group P, n=30), Desflurane 1MAC was used to Group 2 (Group D, n=30) and Sevoflurane to Group 3 (Group S, n=30). Also, rocuronium and remifentanyl infusion were used in maintenance. While desflurane and sevoflurane consumption were recorded from the anesthesia directly, propofol consumption was calculated through the consumption of perfusors and recorded at the end of the surgery. Total cost of anesthetics that used were calculated by multiplying the unit price with their consumption. Apart from these, hemodynamic values of all patients, recovery time, alertness levels in the recovery room (according to Ramsey Scale) were recorded. Results: Significant differences were found between the three groups in terms of cost. While the cost of propofol was significantly lower, it was significantly higher in desfluane group.