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Intubation
Intubation
Intubation is the process of inserting a tube into the trachea to facilitate breathing and administer anesthesia or other medical treatments.
This critical medical procedure is used in a variety of clinical settings, including emergency care, surgery, and intensive care.
Proper intubation technique is essential for patient safety and optimal outcomes.
The PubCompare.ai platform leverages AI to streamline intubation research by locating and comparing protocols from literature, preprints, and patents.
This empowers healthcare professionals to identify the best intubation techniques and products, enhancing reproducibility and accuarcy in this vital area of medical practice.
This critical medical procedure is used in a variety of clinical settings, including emergency care, surgery, and intensive care.
Proper intubation technique is essential for patient safety and optimal outcomes.
The PubCompare.ai platform leverages AI to streamline intubation research by locating and comparing protocols from literature, preprints, and patents.
This empowers healthcare professionals to identify the best intubation techniques and products, enhancing reproducibility and accuarcy in this vital area of medical practice.
Most cited protocols related to «Intubation»
Accidents
Alcoholic Intoxication
Ambulances
Blood Transfusion
Body Regions
Cardiopulmonary Resuscitation
Chest Tubes
Emergencies
Gender
Hospitalization
Injuries
Intubation
Males
Patients
Service, Emergency Medical
Signs, Vital
Woman
Wounds and Injuries
Zinostatin
The Difficult Airway Society commissioned a working group to update the guidelines in April 2012. An initial literature search was conducted for the period January 2002 to June 2012 using databases (Medline, PubMed, Embase, and Ovid) and a search engine (Google Scholar). The websites of the American Society of Anesthesiologists (http://www.asahq.org ), Australian and New Zealand College of Anaesthetists (http://www.anzca.edu.au ), European Society of Anesthesiologists' (http://www.esahq.org/euroanaesthesia ), Canadian Anesthesiologists' Society (http://www.cas.ca ), and the Scandinavian Society of Anesthesiology and Intensive Care Medicine (http://ssai.info/guidelines/ ) were also searched for airway guidelines. English language articles and abstract publications were identified using keywords and filters. The search terms were as follows: ‘Aintree intubating catheter’, ‘Airtraq’, ‘airway device’, ‘airway emergency’, ‘airway management’, ‘Ambu aScope’, ‘backward upward rightward pressure’, ‘Bonfils’, ‘Bullard’, ‘bronchoscopy’, ‘BURP manoeuvre’, ‘can't intubate can't ventilate’, ‘can't intubate can't oxygenate’, ‘C-Mac’, ‘Combitube’, ‘cricoid pressure’, ‘cricothyroidotomy’, ‘cricothyrotomy’, ‘C trach’, ‘difficult airway’, ‘difficult intubation’, ‘difficult laryngoscopy’, ‘difficult mask ventilation’, ‘difficult ventilation’, ‘endotracheal intubation’, ‘esophageal intubation’, ‘Eschmann stylet’, ‘failed intubation’, ‘Fastrach’, ‘fiber-optic scope’, ‘fibreoptic intubation’, ‘fiberoptic scope’, ‘fibreoptic stylet’, ‘fibrescope’ ‘Frova catheter', ‘Glidescope’, ‘gum elastic bougie’, ‘hypoxia’, ‘i-gel’, ‘illuminating stylet’, ‘jet ventilation catheter’, ‘laryngeal mask’, ‘laryngeal mask airway Supreme’, ‘laryngoscopy’, ‘lighted stylet’, ‘light wand’, ‘LMA Supreme’, ‘Manujet’, ‘McCoy’, ‘McGrath’, ‘nasotracheal intubation’, ‘obesity’, ‘oesophageal detector device’, ‘oesophageal intubation’, ‘Pentax airway scope’, ‘Pentax AWS’, ‘ProSeal LMA′, ‘Quicktrach’, ‘ramping’, ‘rapid sequence induction’, ‘Ravussin cannula’, ‘Sanders injector’, ‘Shikani stylet’, ‘sugammadex’, ‘supraglottic airway’, ‘suxamethonium’, ‘tracheal introducer’, ‘tracheal intubation’, ‘Trachview’, ‘Tru view’, ‘tube introducer’, ‘Venner APA’, ‘videolaryngoscope’, and ‘videolaryngoscopy’.
The initial search retrieved 16 590 abstracts. The searches (using the same terms) were repeated every 6 months. In total, 23 039 abstracts were retrieved and assessed for relevance by the working group; 971 full-text articles were reviewed. Additional articles were retrieved by cross-referencing the data and hand-searching. Each of the relevant articles was reviewed by at least two members of the working group. In areas where the evidence was insufficient to recommend particular techniques, expert opinion was sought and reviewed.8 (link) This was most notably the situation when reviewing rescue techniques for the ‘can't intubate can't oxygenate’ (CICO) situation.
Opinions of the DAS membership were sought throughout the process. Presentations were given at the 2013 and 2014 DAS Annual Scientific meetings, updates were posted on the DAS website, and members were invited to complete an online survey about which areas of the existing guidelines needed updating. Following the methodology used for the extubation guidelines,5 (link) a draft version of the guidelines was circulated to selected members of DAS and acknowledged international experts for comment. All correspondence was reviewed by the working group.
The initial search retrieved 16 590 abstracts. The searches (using the same terms) were repeated every 6 months. In total, 23 039 abstracts were retrieved and assessed for relevance by the working group; 971 full-text articles were reviewed. Additional articles were retrieved by cross-referencing the data and hand-searching. Each of the relevant articles was reviewed by at least two members of the working group. In areas where the evidence was insufficient to recommend particular techniques, expert opinion was sought and reviewed.8 (link) This was most notably the situation when reviewing rescue techniques for the ‘can't intubate can't oxygenate’ (CICO) situation.
Opinions of the DAS membership were sought throughout the process. Presentations were given at the 2013 and 2014 DAS Annual Scientific meetings, updates were posted on the DAS website, and members were invited to complete an online survey about which areas of the existing guidelines needed updating. Following the methodology used for the extubation guidelines,5 (link) a draft version of the guidelines was circulated to selected members of DAS and acknowledged international experts for comment. All correspondence was reviewed by the working group.
Airway Management
Anesthesiologist
Anesthetist
Bronchoscopy
Cannula
Catheters
Dyspnea
Emergencies
Eructation
Esophagus
Europeans
Frova
Hypoxia
Intensive Care
Intubation
Intubation, Intratracheal
Laryngoscopy
Light
Medical Devices
Obesity
Pharmaceutical Preparations
Pressure
Rapid Sequence Induction
Scandinavians
Succinylcholine
Sugammadex
Trachea
Tracheal Extubation
Acetaldehyde
Adolescent
Adult
BLOOD
Diet
Ethanol
Food
Immune Tolerance
Intubation
Needles
Oxygen Consumption
Rattus
Reflex, Righting
Serum
Tail
Tube Feeding
Vanilla
Cardiac Arrest
Cardiac Events
Cerebrovascular Accident
Deep Vein Thrombosis
Intubation
Kidney Failure
Kidney Failure, Acute
Myocardial Infarction
Operative Surgical Procedures
Patients
Pneumonia
Pulmonary Embolism
Renal Insufficiency
Septicemia
Surgical Wound Infection
Urinary Tract Infection
Wounds
URECA is an observational birth cohort with planned follow-up through age 7 years. Four research centers (Johns Hopkins University, Baltimore; Boston University and Harvard University, Boston; Columbia University and Mt. Sinai University, New York City; Washington University, St. Louis) are conducting the study. The Administrative Center and Core Laboratories are at the University of Wisconsin-Madison, and Rho Inc. (Chapel Hill, NC) serves as the Statistical and Clinical Coordinating Center. Women were recruited during their pregnancies. Family eligibility required 1) having plans to deliver at an affiliated hospital; 2) biologic mother or father reporting a history of asthma, hay fever, or eczema; and 3) residence in specific urban census tracts in which at least 20% of the population had incomes below the poverty level, as defined by the 2000 U.S. Census.
Newborn eligibility required a gestational age of ≥ 34 weeks and collection of a suitable umbilical cord blood specimen (≥ 5 mL). Maternal human immunodeficiency virus, significant congenital anomalies or infections, intubation or ≥ 4 hours of supplemental oxygen or continuous positive airway pressure for 4 or more days excluded the infant from the study.
Using the same inclusion and exclusion criteria (apart from that for history of allergic disease), a smaller comparison group of children without a parental history of asthma, hayfever, or eczema was also enrolled. These individuals will serve as a reference group to examine the differences in immunologic responses and other study measurements from children with a family history of allergic disease.
Newborn eligibility required a gestational age of ≥ 34 weeks and collection of a suitable umbilical cord blood specimen (≥ 5 mL). Maternal human immunodeficiency virus, significant congenital anomalies or infections, intubation or ≥ 4 hours of supplemental oxygen or continuous positive airway pressure for 4 or more days excluded the infant from the study.
Using the same inclusion and exclusion criteria (apart from that for history of allergic disease), a smaller comparison group of children without a parental history of asthma, hayfever, or eczema was also enrolled. These individuals will serve as a reference group to examine the differences in immunologic responses and other study measurements from children with a family history of allergic disease.
Asthma
Biopharmaceuticals
Birth Cohort
Child
Congenital Abnormality
Continuous Positive Airway Pressure
Eczema
Eligibility Determination
Fever, Hay
Gestational Age
HIV
Hypersensitivity
Infant
Infant, Newborn
Infantile Neuroaxonal Dystrophy
Infection
Intubation
Mothers
Oxygen
Parent
Pregnancy
Specimen Collection
Specimen Collections, Blood
Umbilical Cord
Umbilical Cord Blood
Woman
Most recents protocols related to «Intubation»
Clinical, laboratory, and chest imaging data obtained during COVID-19, other risk factors for severe COVID-19 (Rodrigues et al., 2020 (link); Zhang et al., 2020a (link), 2022a (link); Bennett et al., 2021 (link); Bourgeois et al., 2021 (link); Kooistra et al., 2021 (link); Navaratnam et al., 2021 (link); O’Driscoll et al., 2021 (link); Westblade et al., 2021 (link); Martin et al., 2022a (link); Schober et al., 2022 (link); Woodruff et al., 2022 (link)), and family history were collected for each patient in the survey. Concomitant infections were also recorded, when supported by clinical suspicion, positive cultures, and/or chest x-ray images. Adults with a body mass index (BMI) over 25 were considered to be overweight, and those with a BMI over 30 were considered to be obese. Children aged between 5 and 19 yr were considered to be obese if their BMI-for-age-and-sex was more than 2 SD above the WHO Growth Reference median. Children under 5 yr of age were considered to be obese if their weight-for-height was more than 3 SD above the WHO Child Growth Standard median (WHO, 2021 ).
COVID-19 severity was assessed according to the Human Genetic Effort clinical score (Asano et al., 2021 (link)). SARS-CoV-2 infection was classified as mild/non-confirmed pneumonia (for patients who were asymptomatic, presented upper respiratory tract disease with no signs of pneumonia on x ray or with respiratory symptoms not suggestive of a lower respiratory tract infection and therefore not requiring x ray), moderate (non-hypoxemic pneumonia, not requiring oxygen therapy), severe (hypoxemic pneumonia requiring therapy with oxygen <6 liters O2/min, without meeting the criteria for critical pneumonia) or critical (hypoxemic pneumonia requiring high-flow oxygen >6 liters O2/min, ventilatory support with or without intubation, or ECMO [extracorporeal membrane oxygenation]).
Laboratory values were recorded when available. Normal ranges of laboratory values were reported according to age and are expressed in standard units (Hollowell et al., 2005 (link); Mayo Clinic, 2022 ).
COVID-19 severity was assessed according to the Human Genetic Effort clinical score (Asano et al., 2021 (link)). SARS-CoV-2 infection was classified as mild/non-confirmed pneumonia (for patients who were asymptomatic, presented upper respiratory tract disease with no signs of pneumonia on x ray or with respiratory symptoms not suggestive of a lower respiratory tract infection and therefore not requiring x ray), moderate (non-hypoxemic pneumonia, not requiring oxygen therapy), severe (hypoxemic pneumonia requiring therapy with oxygen <6 liters O2/min, without meeting the criteria for critical pneumonia) or critical (hypoxemic pneumonia requiring high-flow oxygen >6 liters O2/min, ventilatory support with or without intubation, or ECMO [extracorporeal membrane oxygenation]).
Laboratory values were recorded when available. Normal ranges of laboratory values were reported according to age and are expressed in standard units (Hollowell et al., 2005 (link); Mayo Clinic, 2022 ).
Adult
Chest
Child
Clinical Laboratory Services
COVID 19
Extracorporeal Membrane Oxygenation
Index, Body Mass
Infection
Intubation
Obesity
Patients
Pneumonia
Radiography
Respiratory Tract Diseases
Respiratory Tract Infections
Signs and Symptoms, Respiratory
Therapies, Oxygen Inhalation
This is a cross-sectional, retrospective, and descriptive study. Data was gathered from all patients admitted to the emergency department of Sírio-Libanês Hospital (São Paulo, Brazil) presenting with COVID-19 symptoms and cutaneous manifestations, between February and June 2020. Individuals who did not require hospitalization, and showing mild to moderate COVID-19 symptoms, were evaluated by a dermatologist only during the period of care in the emergency department. Patients requiring hospitalization were followed up by physicians from the dermatology team throughout the full length of in-hospital time. Whenever consent was given, skin lesions were photographed without any identification of the specific patient. Cases were selected according to the following criteria: 1) Subjects with COVID-19 symptoms, regardless of severity, 2) A positive nose swab (PCR test) for COVID-19; 3) Presence of skin lesions of recent onset (previous 2 weeks) documented by photo, at the time of the clinical evaluation in the emergency department, or during the hospitalization period. Skin biopsy was not performed routinely, being utilized only in cases demanding additional anatomopathological examination for diagnostic elucidation, abiding by institutional norms of consent agreed by the patient. Information originated from medical records included age at disease onset, gender, clinical features of COVID-19, and relevant medical history. The cutaneous manifestations were described by dermatologists according to the patterns of skin lesions. It was also recorded the topography, and the time of onset in relation to the COVID-19 symptoms, as well as the symptoms associated with the dermatological findings. Prognostic factors of possible worse outcomes were also analyzed in hospitalized patients, such as the need for non-invasive ventilation, intubation, dialysis, Extracorporeal Membrane Oxygenation (ECMO), and death.
Microsoft Excel® was used as the data sheet template, allowing analysis for descriptive statistics. The continuous variables were presented as mean, median, minimum, and maximum values, and Standard Deviation (SD); while the categorical variables were presented as absolute (n) and relative (%) frequencies. Statistical analysis was performed using IBM SPSS Statistics Version 24 and statistical significance was set at 5% (p < 0.05). The inferential analyzes used in order to confirm or refute evidence found in the descriptive analysis were t-Student for independent samples, Mann-Whitney, Analysis of Variance (ANOVA) with one factor Fixed, Kruskal-Wallis, Pearson's Chi-Square and Fisher's Exact or its extension.
This study was approved by the Ethics Committee of Sírio-Libanês Hospital, under the number 32840120.4.0000.5461, and written informed consent was obtained from all the participants.
Microsoft Excel® was used as the data sheet template, allowing analysis for descriptive statistics. The continuous variables were presented as mean, median, minimum, and maximum values, and Standard Deviation (SD); while the categorical variables were presented as absolute (n) and relative (%) frequencies. Statistical analysis was performed using IBM SPSS Statistics Version 24 and statistical significance was set at 5% (p < 0.05). The inferential analyzes used in order to confirm or refute evidence found in the descriptive analysis were t-Student for independent samples, Mann-Whitney, Analysis of Variance (ANOVA) with one factor Fixed, Kruskal-Wallis, Pearson's Chi-Square and Fisher's Exact or its extension.
This study was approved by the Ethics Committee of Sírio-Libanês Hospital, under the number 32840120.4.0000.5461, and written informed consent was obtained from all the participants.
Biopsy
COVID 19
Dermatologist
Diagnosis
Dialysis
Emergencies
Ethics Committees, Clinical
Extracorporeal Membrane Oxygenation
Gender
Hospitalization
Intubation
Noninvasive Ventilation
Nose
Patients
Physicians
Prognostic Factors
Skin
Skin Manifestations
Student
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Acute Hypoxemic Respiratory Failure
Adrenal Cortex Hormones
Antigens
Biological Assay
Cell Respiration
Clinical Protocols
Coronavirus
COVID 19
Critical Care
Delirium
Diagnosis
Heart
Intubation
Lung
Medical Devices
Muscle Tissue
Nose
Patients
Pharmaceutical Preparations
Real-Time Polymerase Chain Reaction
Respiratory Distress Syndrome, Acute
Respiratory Rate
Rest, Bed
RNA-Directed DNA Polymerase
Self Mutilation
Therapeutics
Ventilator-Induced Lung Injury
The patients received their usual cardiac medications in the early morning on the day of surgery. Upon arriving OR, the patients were premedicated with midazolam 0.02 mg/kg and fentanyl 1 mcg/kg. A five-lead EKG, pulse oximetry, and noninvasive blood pressure monitoring were initiated. Then, we inserted a catheter into the radial artery under local anesthesia for invasive blood pressure monitoring. General anesthesia induction consisted of fentanyl 5–10 mcg/kg, midazolam 0.2–0.4 mg/kg, and pancuronium 0.1–0.15 mg/kg. Additionally, propofol 0.5–1 mg/kg was administered as appropriate. After intubation, we inserted a right internal jugular multilumen central venous catheter. Maintenance of anesthesia was with sevoflurane 1%–2%, adjusted by clinical conditions and pancuronium as needed.
Anesthesia
Arteries, Radial
Blood Pressure
Catheters
Fentanyl
General Anesthesia
Heart
Intubation
Local Anesthesia
Midazolam
Oximetry, Pulse
Pancuronium
Patients
Pharmaceutical Preparations
Propofol
Sevoflurane
Surgery, Day
Training Programs
Venous Catheter, Central
Hospitalized patients aged 18 years or older with pelvic or sacral tumors who were scheduled for sacrectomy or pelvic resection were screened from the operation list. Exclusion criteria were existing diagnoses of major psychiatric disorders, surgery cancellation, an anticipated postoperative intubation longer than 24 hours, inability to read or write, or inability to give informed consent. All patients underwent surgery under general anesthesia at Peking University People’s Hospital between January 2020 and July 2021.
Anesthesia
Diagnosis
General Anesthesia
Intubation
Mental Disorders
Neoplasms
Operative Surgical Procedures
Patients
Pelvis
Sacrum
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More about "Intubation"
Intubation is the process of inserting a tube, or endotracheal tube (ETT), into the trachea to facilitate breathing and administer anesthesia, oxygen, or other medical treatments.
This critical medical procedure is used in a variety of clinical settings, including emergency care, surgery, and intensive care units (ICUs).
Proper intubation technique is essential for patient safety and optimal outcomes.
The intubation process involves the insertion of a laryngoscope to visualize the vocal cords, followed by the placement of the ETT through the vocal cords and into the trachea.
This procedure can be performed using various techniques, such as direct laryngoscopy, video laryngoscopy, or fiber-optic intubation.
The choice of intubation method often depends on the patient's anatomy, clinical condition, and the healthcare provider's expertise.
Intubation is a vital skill for healthcare professionals, including emergency medical technicians (EMTs), paramedics, anesthesiologists, critical care physicians, and emergency room (ER) staff.
Proper training and regular practice are essential to ensure proficiency and minimize the risk of complications, such as airway trauma, esophageal intubation, or hypoxia.
The PubCompare.ai platform leverages artificial intelligence (AI) to streamline intubation research by locating and comparing protocols from literature, preprints, and patents.
This empowers healthcare professionals to identify the best intubation techniques and products, enhancing reproducibility and accuracy in this critical area of medical practice.
Synonyms and related terms for intubation include tracheal intubation, endotracheal intubation, orotracheal intubation, nasotracheal intubation, and airway management.
Abbreviations commonly used include ETT, LMA (laryngeal mask airway), and CICO (can't intubate, can't oxygenate).
Key subtopics in intubation research and practice include airway anatomy, intubation techniques, equipment and devices (e.g., laryngoscopes, ETTs, video laryngoscopes), complications and management, and training and education.
Relevant software and tools used in intubation research and practice include SAS version 9.4, Stata 14, SPSS Statistics version 25, and R version 4.0.2.
Isoflurane, a volatile anesthetic, and Rompun, a sedative and analgesic, are sometimes used in conjunction with intubation procedures, particularly in veterinary or animal research settings.
The Model 683 ventilator is also a commonly used device in intubation and mechanical ventilation.
This critical medical procedure is used in a variety of clinical settings, including emergency care, surgery, and intensive care units (ICUs).
Proper intubation technique is essential for patient safety and optimal outcomes.
The intubation process involves the insertion of a laryngoscope to visualize the vocal cords, followed by the placement of the ETT through the vocal cords and into the trachea.
This procedure can be performed using various techniques, such as direct laryngoscopy, video laryngoscopy, or fiber-optic intubation.
The choice of intubation method often depends on the patient's anatomy, clinical condition, and the healthcare provider's expertise.
Intubation is a vital skill for healthcare professionals, including emergency medical technicians (EMTs), paramedics, anesthesiologists, critical care physicians, and emergency room (ER) staff.
Proper training and regular practice are essential to ensure proficiency and minimize the risk of complications, such as airway trauma, esophageal intubation, or hypoxia.
The PubCompare.ai platform leverages artificial intelligence (AI) to streamline intubation research by locating and comparing protocols from literature, preprints, and patents.
This empowers healthcare professionals to identify the best intubation techniques and products, enhancing reproducibility and accuracy in this critical area of medical practice.
Synonyms and related terms for intubation include tracheal intubation, endotracheal intubation, orotracheal intubation, nasotracheal intubation, and airway management.
Abbreviations commonly used include ETT, LMA (laryngeal mask airway), and CICO (can't intubate, can't oxygenate).
Key subtopics in intubation research and practice include airway anatomy, intubation techniques, equipment and devices (e.g., laryngoscopes, ETTs, video laryngoscopes), complications and management, and training and education.
Relevant software and tools used in intubation research and practice include SAS version 9.4, Stata 14, SPSS Statistics version 25, and R version 4.0.2.
Isoflurane, a volatile anesthetic, and Rompun, a sedative and analgesic, are sometimes used in conjunction with intubation procedures, particularly in veterinary or animal research settings.
The Model 683 ventilator is also a commonly used device in intubation and mechanical ventilation.