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      Serious Adverse Events in Pediatric Procedural Sedation Before and After the Implementation of a Pre-Sedation Checklist

      1 , 2

      Journal of Pain Research

      Dove

      sedation, checklist, adverse events, pediatric

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          Abstract

          Objective

          Procedural sedation is considered by the Joint Commission on Accreditation of Healthcare Organizations as a high-risk procedure when performed in the emergency department (ED). A pre-sedation checklist is a set of items checked before any sedation. We evaluated the impact of a pre-sedation checklist on the rate of serious adverse events (SAE) in a pediatric ED.

          Methods

          We conducted a retrospective study comparing the rate of SAE in children treated with the combination of ketamine and propofol before and after the implementation of a pre-sedation checklist. The before-and-after periods lasted from 1.1.2013 to 30.6.2016 and from 1.7.2016 to 30.6.2019, respectively. Patient data were extracted from the electronic medical records using an integrated business intelligence information system.

          Results

          The before-and-after cohorts included 1349 and 1846 patients, respectively. The two groups were similar with regard to age, sex, length and type of procedure, medications dosage, and level of physicians’ training. A total of 183/1349 (13.5%) and 420/1846 (22.7%) SAE were recorded during the before-checklist and after-checklist periods, respectively (p<0.0001). The rates of laryngospasm, apnea, and oxygen saturation ≤90% at the before-and-after checklist periods were 9/1349 (0.6%) and 30/1846 (1.6%); p<0.05, 48/1349 (3.5%) and 77/1846 (4.2%); p=0.37, and 123/1349 (9.1%) and 312/1846 (16.9%); p< 0.0001, respectively. All the SAE were successfully managed by the emergency physicians and no patient required hospitalization due to a SAE.

          Conclusion

          In this large cohort of ED children who underwent deep sedation, the administration of a pre-sedation checklist was not associated with a reduction in SAE rate.

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          Most cited references 15

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          International Standards for a Safe Practice of Anesthesia 2010

          These standards1 are recommended for anesthesia professionals throughout the world. They are intended to provide guidance and assistance to anesthesia professionals, their professional societies, hospital and facility administrators, and governments for improving and maintaining the quality and safety of anesthesia care. They were adopted by the World Federation of Societies of Anaesthesiologists on the 13th June 1992, and revisions were ratified on 5th March 2008 and on 19th March 2010. For some anesthesia services, groups, and departments these standards will represent a future goal, while for others they may already have been implemented and be regarded as mandatory. It is recognized that in some settings facing challenges in resources and organization, not even those standards regarded as mandatory are met at present. The provision of anesthesia under such circumstances should be restricted to procedures which are absolutely essential for the urgent or emergency saving of life or limb, and every effort should be made by those responsible for the provision of healthcare in these areas and settings to ensure that the standards are met. Provision of anesthesia care at standards lower than those outlined as mandatory for anesthesia for elective surgical procedures simply cannot be construed as safe acceptable practice. The most important standards relate to individual anesthesia professionals. Monitoring devices play an important part in safe anesthesia as extensions of human senses and clinical skills rather than their replacement. Adopting the standardized language of the World Health Organization, minimum standards that would be expected in all anesthesia care for elective surgical procedures are termed “ HIGHLY RECOMMENDED ” and these are the functional equivalent of “mandatory” standards. These HIGHLY RECOMMENDED standards, indicated in bold type , are applicable throughout any elective procedure, from patient evaluation until recovery (it is recognized, however, that immediate life-saving measures always take precedence in an emergency). In the judgement of the WFSA, these are the minimum standards for anesthesia for a “necessary” procedure (rather than essential and/or emergency) in settings where resources are extremely limited. This does not imply that these standards on their own are ideal or even acceptable in more adequately resourced settings. These HIGHLY RECOMMENDED (functional equivalent of mandatory) standards and (regarding facilities, equipment, and medications) the parallel prescription for “Level 1” or “basic” infrastructure are relevant to any healthcare environment anywhere in which general or regional anesthetics are administered, but not to a setting where superficial procedures involving local anesthetics only are performed. Additional elements of the anesthesia standards should be implemented as resources, organization, and training permit, yielding this paradigm:   Anesthesia standards (in order of adoption) Setting Infrastructure HIGHLY RECOMMENDED Level 1 Basic HIGHLY RECOMMENDED + RECOMMENDED Level 2 Intermediate HIGHLY RECOMMENDED + RECOMMENDED + Suggested Level 3 Optimal See Table 1 for a detailed outline of the integration of the practice standards with the levels of facilities/infrastructure. The goal always in any setting is to practice to the highest possible standards, specifically exceeding those prescribed if that can be accomplished. In spite of some facilities’ limitations, it may be possible to implement elements of the RECOMMENDED standards even in a “basic” setting and, likewise, to implement elements of the Suggested standards even in an “intermediate” setting. The goal is always the best care possible and ongoing improvement by meeting and exceeding the standards for safe practice of anesthesia, starting with all providers meeting the HIGHLY RECOMMENDED standards and striving to meet as many of the RECOMMENDED and Suggested standards as well. Table 1 Guide to Infrastructure, Supplies and Anesthesia Standards at Three Levels of Health Care Facility Infrastructure and Supplies Level 1 (Should meet at least HIGHLY RECOMMENDED anesthesia standards) Small hospital / health centre Level 2 (Should meet at least HIGHLY RECOMMENDED and RECOMMENDED anesthesia standards) District/provincial hospital Level 3 (Should meet at least HIGHLY RECOMMENDED, RECOMMENDED and SUGGESTED anesthesia standards) Referral hospital Rural hospital or health centre with a small number of beds (or urban location in an extremely disadvantaged area); sparsely equipped operating room (OR) for “minor” proceduresProvides emergency measures in the treatment of 90–95% of trauma and obstetrics cases (excluding cesarean section)Referral of other patients (for example, obstructed labour, bowel obstruction) for further management at a higher level District or provincial hospital (e.g. with100–300 beds) and adequately equipped major and minor operating roomsShort term treatment of 95–99% of the major life threatening conditions A referral hospital of 300–1000 or more beds with basic intensive care facilities. Treatment aims are the same as for Level 2, with the addition of: Ventilation in OR and ICUProlonged endotracheal intubationThoracic trauma careHemodynamic and inotropic treatmentComplex neurological and cardiac surgeryBasic ICU patient management and monitoring for up to 1 week : all types of cases, but possibly with limited provision for: Multi-organ system failureHemodialysisProlonged respiratory failureMetabolic care or monitoring Essential Procedures Essential Procedures Essential Procedures Normal deliveryUterine evacuationCircumcisionHydrocele reduction, incision and drainageWound suturingControl of hemorrhage with pressure dressingsDebridement and dressing of woundsTemporary reduction of fracturesCleaning or stabilization of open and closed fracturesChest drainage (possibly) Abscess drainage Same as Level 1 with the following additions: Cesarean sectionLaparotomy (usually not for bowel obstruction)AmputationHernia repairTubal ligationClosed fracture treatment and application of plaster of ParisAcute open orthopedic surgery: e.g internal fixation of fracturesEye operations, including cataract extractionRemoval of foreign bodies: e.g. in the airwayEmergency ventilation and airway management for referred patients such as those with chest and head injuries Same as Level 2 with the following additions:Facial and intracranial surgeryBowel surgeryPediatric and neonatal surgeryThoracic surgeryMajor eye surgeryMajor gynecological surgery, e.g. vesico-vaginal repair Personnel Personnel Personnel Paramedical staff/anesthetic officer (including on-the-job training) who may have other duties as wellNurse-midwife One or more trained anesthesia professionalsDistrict medical officers, senior clinical officers, nurses, midwivesVisiting specialists or resident surgeon and/or obstetrician/ gynecologist Clinical officers and specialists in anesthesia and surgery Drugs Drugs Drugs Ketamine 50 mg/ml injectionLidocaine 1% or 2%Diazepam 5 mg/ml injection, 2 ml or midazolam 1 mg/ml injection, 5 mlPethidine 50 mg/ml injection, 2 mlMorphine 10 mg/ml, 1 mlEpinephrine (Adrenaline) 1 mgAtropine 0.6 mg/mlAppropriate inhalation anesthetic if vaporizer available Same as Level 1, but also:Thiopental 500 mg/1 g powder or propofol.Suxamethonium bromide 500 mg powderPancuroniumNeostigmine 2.5 mg injectionEther, halothane or other inhalation anestheticsLidocaine 5% heavy spinal solution, 2 mlBupivacaine 0.5% heavy or plain, 4 mlHydralazine 20 mg injection Same as Level 2 with these additions:PropofolNitrous oxideVarious modern neuromuscular blocking agentsVarious modern inhalation anestheticsVarious inotropic agentsVarious intravenous antiarrhythmic agentsNitroglycerine for infusionCalcium chloride 10% 10 im injection Furosemide 20 mg injectionDextrose 50% 20 ml injectionAminophylline 250 mg injectionEphedrine 30/50 mg ampoulesHydrocortisone(?) Nitrous oxide Potassium chloride 20% 10 ml injection for infusion Equipment: capital outlay Equipment: capital outlay Equipment: capital outlay Adult and pediatric self-inflating breathing bags with masksFoot-powered suctionStethoscope, sphygmomanometer, thermometerPulse oximeterOxygen concentrator or tank oxygen and a draw-over vaporizer with hoses Complete anesthesia, resuscitation and airway management systems including: Reliable oxygen sourcesVaporizer(s)Hoses and valvesBellows or bag to inflate lungsFace masks (sizes 00–5)Work surface and storagePediatric anesthesia systemOxygen supply failure alarm; oxygen analyzer Same as Level 2 with these additions (per operating room or per ICU bed, except where stated):ECG (electrocardiograph) monitor*Anesthesia ventilator, reliable electric power source with manual overrideInfusion pumps (2 per bed)Pressure bag for IV infusionElectric or pneumatic suctionOxygen analyzer* Laryngoscopes, bougies Adult and pediatric resuscitator setsPulse oximeter, spare probes, adult and pediatric*Capnograph*Defibrillator (one per O.R. suite / ICU)*ECG (electrocardiograph) monitor*Laryngoscope, Macintosh blades 1-3(4)Oxygen concentrator[s] [cylinder]Foot or electric suctionIV pressure infusor bagAdult and pediatric resuscitator setsMagill forceps (adult and child), intubation stylet and/or bougieSpinal needles 25GNerve stimulatorAutomatic non-invasive blood pressure monitor Thermometer [temperature probe*]Electric warming blanketElectric overhead heaterInfant incubatorLaryngeal mask airways sizes 2, 3, 4 (3 sets per O.R)Intubating bougies, adult and child (1 set per O.R)Anesthetic agent (gas and vapour) analyserDepth of anesthesia monitors are being increasingly recommended for cases at high risk of awareness but are not standard monitoring in many countries. Equipment: disposable Equipment: disposable Equipment: disposable Examination glovesIV infusion/drug injection equipment ECG electrodesIV equipment (minimum fluids: normal saline, Ringer’s lactate and dextrose 5%) Same as Level 2 with these additions:Ventilator circuits Suction catheters size 16 FG Pediatric giving sets Yankauer suckers Airway support equipment, including airways and tracheal tubes Suction catheters size 16 FGSterile gloves sizes 6–8 Giving sets for IV infusion pumpsDisposables for suction machines Oral and nasal airways Nasogastric tubes sizes 10–16 FGOral airways sizes 000–4Tracheal tubes sizes 3–8.5 mmSpinal needles sizes 22 G and 25GBatteries size C Disposables for capnography, oxygen analyzer, in accordance with manufacturers’ specifications:Sampling linesWater trapsConnectorsFilters – Fuel cells * It is preferable to combine these modalities all in one unit Note: drug concentrations and quantities are indicative only. All equipment should be appropriate for patients’ age and size It is anticipated that these standards and the setting/infrastructure specifications will be revised as practice and technology evolve. International Standards for a Safe Practice of Anesthesia 2010 General standards 1. Professional status Anesthesia services are a vital component of basic healthcare requiring appropriate resources. The WFSA views anesthesia as a medical practice. Medically trained anesthesia specialists should be trained and accredited with clinical and administrative autonomy. When anesthesia is provided by non-medical personnel, these providers should be appropriately trained and accredited as well as directed and supervised by medically qualified specialist anesthesia professionals. 2. Professional organizations Anesthesia professionals should form appropriate organizations at local, regional, and national levels for the setting of standards of practice, supervision of training and continuing education/continuing professional development with appropriate certification and accreditation, and general promotion of anesthesia as an independent professional specialty. These organizations should form links with appropriate groups within the region and/or country and internationally. 3. Training, certification, and accreditation Adequate time, facilities, and financial support should be available for professional training, both initial and continuing, to ensure that an adequate standard of knowledge, expertise, and practice is attained and maintained. Formal certification of training and accreditation to practice is RECOMMENDED. 4. Records and statistics A record of the details of each anesthetic should be made and preserved with the patient’s medical record. This should include details of the pre-operative assessment and the post-operative course. It is RECOMMENDED that individuals, departments, and regional and national groups collect cumulative data to facilitate the progressive enhancement of the safety, efficiency, effectiveness, and appropriateness of anesthesia care. 5. Peer review and incident reporting Institutional, regional, and/or national mechanisms to provide a continuing review of anesthetic practice should be instituted. Regular confidential discussion of appropriate topics and cases with multidisciplinary professional colleagues should take place. Protocols should be developed to ensure that deficiencies in individual and collective practice are identified and rectified. An anonymous incident reporting system with case analysis and resulting suggested remedies is RECOMMENDED. 6. Workload A sufficient number of trained anesthesia professionals should be available so that individuals may practice to a high standard without undue fatigue or physical demands. Time should be allocated for education, professional development, administration, research, and teaching. 7. Personnel An anesthesia professional should be dedicated to each patient and be immediately present throughout each anesthetic (general, regional, or monitored sedation), and should be responsible for the transport of the patient to the post-anesthesia recovery facility and the transfer of care to appropriately trained personnel. An anesthesia professional should retain overall responsibility for the patient during the recovery period and should be readily available for consultation until the patient has made an adequate recovery. If responsibility for care is transferred from one anesthesia professional to another, a “handover protocol” should be followed, during which all relevant information about the patient’s history, medical condition, anesthetic status, and plan should be communicated. An anesthesia professional should ensure, if aspects of direct care are delegated before, during, or after an anesthetic, that the person to whom responsibility is delegated is both suitably qualified and conversant with relevant information regarding the anesthetic and the patient. Where it is impossible for this standard to be attained and the surgeon or other individual assumes responsibility for the anesthetic, these arrangements should be reviewed and audited by an appropriately trained anesthesia professional. 8. Facilities, equipment, and medications Appropriate equipment and facilities, adequate both in quantity and quality, should be present wherever anesthesia and recovery from it is undertaken, including outside traditional hospital operating room suites, such as procedure or imaging suites and outpatient facilities or offices. In-service training and verification of an individual’s ability to use a specific piece of equipment correctly and safely is required. Formal certification as documentation of this process is Suggested. A list of facilities, infrastructure elements and supplies at the three levels and suggestions as to the order in which additions should be made when possible as resources permit is presented in Table 1. Anesthesia equipment should conform to relevant national and international standards. Appropriate anesthetic, resuscitative, and adjuvant medications are required at each level. 9. World Health Organization 2009 Safe Surgery Checklist The 2009 Safe Surgery Checklist (http://www.who.int/patientsafety/information_centre/documents/en/index.html) consists of evidence based vital checks in 3 phases: before starting anesthesia, before starting surgery and at the end of surgery. The use of the checklist (locally modified if appropriate) in anesthesia care is HIGHLY RECOMMENDED. Peri-anesthetic care and monitoring standards The first and most important component of peri-anesthetic care, including monitoring of the anesthesia delivery system and the patient, is the continuous presence of a vigilant anesthesia professional during anesthesia. In addition to use of monitoring technology, careful continuous clinical observation is required because equipment may not detect clinical deterioration as rapidly as the skilled professional. If an emergency requires the brief temporary absence of the primary anesthesia professional, judgment must be exercised comparing the emergency with the anesthetized patient’s condition and in the selection of the person left responsible for the anesthetic during the temporary absence. 1. Pre-anesthetic care The patient must be evaluated by an anesthesia professional prior to administration of anesthesia and an appropriate anesthetic plan formulated. The anesthesia professional must ensure that all necessary equipment is present and functions correctly prior to initiation of anesthesia care. The anesthesia professional should ensure that assistance is available as needed and that the assistant is competent at, or has been instructed in, the necessary tasks. The development of protocols and check-lists to facilitate such verification is RECOMMENDED. 2. Pre-anesthesia checks An appropriate “pre-list check,” which has been established in each health care institution providing anesthesia services, of the anesthesia system, facilities, equipment, and supplies should be performed prior to the start of each operating list. The relevant components of the World Health Organization Safe Surgery Checklist should be performed. An appropriate “pre-patient check” (such as presented in the attached Pre-anesthetic check list) which has been established in each health care institution providing anesthesia services, of the anesthesia system and anesthetizing location should be executed prior to each anesthetic. *The integrity of a circle system and its valves should be checked by placing one breathing bag in the correct place for ventilating a patient and another breathing bag on the patient limb of the Y-piece (i.e. in place of the patient) and ventilating the system manually using an appropriate fresh gas flow and squeezing the primary and secondary bags alternatively, so that gas passes around the circle from one to the other. Inflation and deflation of the breathing bag, movement of any visible unidirectional valves, and the resistance and compliance of the system should all be assessed as “normal”. The function of the adjustable pressure limiting valve should also be checked by spilling some of the gas when both bags are compressed. This “two bag check” is a reliable way of detecting expiratory limb obstruction which is readily missed when less systematic checks of the integrity of the circuit are carried out. 3. Monitoring during anesthesia A. Oxygenation (i) Oxygen supply Supplemental oxygen is HIGHLY RECOMMENDED for all patients undergoing general anesthesia. The anesthesia professional should verify the integrity of the oxygen supply. It is RECOMMENDED that the inspired oxygen concentration be monitored throughout each anesthetic with an instrument fitted with a low oxygen concentration alarm. An oxygen supply failure alarm and a device protecting against the delivery of an hypoxic gas mixture are RECOMMENDED. Systems with interlocks (tank yokes, hose connections, etc.) should be used to prevent misconnection of gas sources. (ii) Oxygenation of the patient Tissue oxygenation should be monitored continuously. For visual examination, adequate illumination and exposure of the patient should be ensured whenever practicable. Continuous use of pulse oximetry is HIGHLY RECOMMENDED. B. Airway and ventilation The adequacy of the airway and ventilation should be continuously monitored at least by observation and auscultation whenever practicable. Where a breathing circuit is used, the reservoir bag should be observed. Continuous monitoring with a precordial, pretracheal, or oesophageal stethoscope is RECOMMENDED. Confirmation of the correct placement of an endotracheal tube and also the adequacy of ventilation by continuous measurement and display of the expired carbon dioxide waveform and concentration (capnography) is RECOMMENDED . When mechanical ventilation is employed, a “disconnect alarm” should be used throughout the period of mechanical ventilation. Continuous measurement of the inspiratory and/or expired gas volumes, and of the concentration of volatile agents, is Suggested. C. Circulation (i) Cardiac rate and rhythm The circulation should be monitored continuously. Palpation or display of the pulse and/or auscultation of the heart sounds should be continuous. Continuous monitoring and display of the heart rate with a pulse oximeter is HIGHLY RECOMMENDED; an electrocardiograph is RECOMMENDED. The availability of a defibrillator is RECOMMENDED. (ii) Tissue perfusion The adequacy of tissue perfusion should be monitored continually by clinical examination. Continuous monitoring with a pulse oximeter is HIGHLY RECOMMENDED; continuous monitoring with a capnograph is RECOMMENDED. (iii) Blood pressure Arterial blood pressure should be determined at appropriate intervals (usually at least every 5 minutes and more frequently if indicated by clinical circumstances). Automated non-invasive blood pressure measurements have many advantages in anesthesia; continuous measurement and display of arterial pressure is Suggested in appropriate cases. D. Temperature A means of measuring the temperature should be available and should be used at frequent intervals where clinically indicated (e.g. prolonged or complex anesthetics, young children). The continual measurement of temperature in patients in whom a change is anticipated, intended, or suspected is RECOMMENDED. The availability and use of continuous electronic temperature measurement is Recommended. E. Neuromuscular function When neuromuscular blocking drugs are given, the use of a peripheral nerve stimulator is RECOMMENDED. F. Depth of anesthesia The depth of anesthesia (degree of unconsciousness) should be regularly assessed by clinical observation. The continuous measurement of inspired and expired concentrations of anesthetic gases and volatile agents is Suggested. The application of an electronic device intended to measure brain function (consciousness), while controversial and not universally recommended, should be considered, particularly in cases with high risk of awareness under general anesthesia. G. Audible signals and alarms Available audible signals (such as the variable pitch pulse tone of the pulse oximeter) and audible alarms (with appropriately set limit values) should be activated at all times and loud enough to be heard throughout the operating room. 4. Post-anesthesia care A. Facilities and personnel All patients who have had an anesthetic affecting central nervous system function and/or a loss of protective reflexes should remain where anesthetized until recovered or be transported safely (with care and monitoring as indicated) to a specifically designated recovery location for post-anesthesia recovery. See General Standards, Section 7, for delegation of responsibilities to dedicated qualified recovery personnel. B. Monitoring All patients should be observed and monitored in a manner appropriate to the state of their nervous system function, vital signs, and medical condition with emphasis on the adequacy of oxygenation, ventilation, circulation, and temperature. Supplementation of clinical monitoring with quantitative methods analogous to intra-anesthetic patient care described above is RECOMMENDED. Specifically, pulse oximetry is HIGHLY RECOMMENDED until consciousness has recovered (i.e. the patient is no longer anesthetized). C. Pain relief All patients are entitled to appropriate efforts to prevent and alleviate postoperative pain employing available appropriate medications and modalities; these efforts are therefore HIGHLY RECOMMENDED. Usually, the involved anesthesia professional assumes initial responsibility for this.
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            Consensus-based recommendations for standardizing terminology and reporting adverse events for emergency department procedural sedation and analgesia in children.

            Children commonly require sedation and analgesia for procedures in the emergency department. Establishing accurate adverse event and complications rates from the available literature has been difficult because of the difficulty in aggregating results from previous studies that have used varied terminology to describe the same adverse events and outcomes. Further, serious adverse events occur infrequently, necessitating the study of large numbers of children to assess safety. These limitations prevent the establishment of a sufficiently large database on which evidence-based practice guidelines may be based. We assembled a panel of pediatric sedation researchers and experts to develop consensus-based recommendations for standardizing procedural sedation and analgesia terminology and reporting of adverse events. Our goal was to create a uniform reporting mechanism for future studies to facilitate the aggregation and comparison of results.
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              Can You Multitask? Evidence and Limitations of Task Switching and Multitasking in Emergency Medicine.

              Emergency physicians work in a fast-paced environment that is characterized by frequent interruptions and the expectation that they will perform multiple tasks efficiently and without error while maintaining oversight of the entire emergency department. However, there is a lack of definition and understanding of the behaviors that constitute effective task switching and multitasking, as well as how to improve these skills. This article reviews the literature on task switching and multitasking in a variety of disciplines-including cognitive science, human factors engineering, business, and medicine-to define and describe the successful performance of task switching and multitasking in emergency medicine. Multitasking, defined as the performance of two tasks simultaneously, is not possible except when behaviors become completely automatic; instead, physicians rapidly switch between small tasks. This task switching causes disruption in the primary task and may contribute to error. A framework is described to enhance the understanding and practice of these behaviors.
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                Author and article information

                Journal
                J Pain Res
                J Pain Res
                JPR
                jpainres
                Journal of Pain Research
                Dove
                1178-7090
                17 July 2020
                2020
                : 13
                : 1797-1802
                Affiliations
                [1 ]Rappaport Faculty of Medicine, Technion-Institute of Technology , Haifa, Israel
                [2 ]Emergency Department, Ruth Children’s Hospital, Rambam Health Care Campus , Haifa, Israel
                Author notes
                Correspondence: Itai Shavit POB 274, Kibutz Maayan Tzvi, 3080500, IsraelTel +972-50-2063239Fax +972-4-8543109 Email itai@pem-database.org
                Article
                262354
                10.2147/JPR.S262354
                7381781
                © 2020 Librov and Shavit.

                This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License ( http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms ( https://www.dovepress.com/terms.php).

                Page count
                Figures: 1, Tables: 1, References: 19, Pages: 6
                Funding
                Funded by: No honorarium, grant, or other form of payment
                For the 2 authors, there are no potential conflicts of interest, real or perceived in the study design, the collection, analysis, and interpretation of data, the writing of the report, and the decision to submit the paper for publication. No honorarium, grant, or other form of payment was given to anyone to produce the manuscript. The authors have no conflict of interest.
                Categories
                Original Research

                Anesthesiology & Pain management

                pediatric, adverse events, checklist, sedation

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