Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 8 de 8
Filter
1.
Rev Esp Anestesiol Reanim (Engl Ed) ; 68(8): 437-442, 2021 Oct.
Article in English | MEDLINE | ID: mdl-34538618

ABSTRACT

OBJECTIVES: The disease COVID-19 produces serious complications that can lead to cardiorespiratory arrest. Quality cardiopulmonary resuscitation (CPR) can improve patient prognosis. The objective of this study is to evaluate the performance of the specialty of Anesthesiology in the management of CPR during the pandemic. METHODS: A survey was carried out with Google Forms consisting of 19 questions. The access link to the questionnaire was sent by email by the Spanish Society of Anesthesia (SEDAR) to all its members. RESULTS: 225 responses were obtained. The regions with the highest participation were: Madrid, Catalonia, Valencia and Andalusia. 68.6%% of the participants work in public hospitals. 32% of the participants habitually work in intensive care units (ICU), however, 62.1% have attended critical COVID-19 in the ICU and 72.6% have anesthetized them in the operating room. 26,3% have attended some cardiac arrest, 16,8% of the participants admitted to lead the manoeuvres, 16,8% detailed that it had been another department, and 66,2% was part of the team, but did not lead the assistance. Most of the CPR was performed in supine, only 5% was done in prone position. 54.6% of participants had not taken any course of Advance Life Support (ALS) in the last 2 years. 97.7% of respondents think that Anesthesia should lead the in-hospital CPR. CONCLUSION: The specialty of Anesthesiology has actively participated in the care of the critically ill patient and in the management of CPR during the COVID-19 pandemic. However, training and/or updating in ALS is required.


Subject(s)
COVID-19 , Cardiopulmonary Resuscitation , Heart Arrest , Heart Arrest/therapy , Humans , Pandemics , Prognosis , SARS-CoV-2 , Spain/epidemiology
2.
Rev. esp. anestesiol. reanim ; 61(3): 133-139, mar. 2014.
Article in English | IBECS | ID: ibc-119962

ABSTRACT

Introduction and objective Occupational exposure to sevoflurane should not exceed 2 ppm. During inhalation sedation with sevoflurane using the anaesthetic conserving device (AnaConDa®) in the post-anaesthesia care unit, waste gases can be reduced by gas extraction systems or scavenging devices such as CONTRAfluran™. However, the efficacy of these methods has not been clearly established. To determine the safest scenario for healthcare workers during inhalation sedation with sevoflurane in the post-surgical intensive care unit. Materials and methods: An experimental study on occupational exposure was conducted in a post-cardiothoracic care unit during March-August 2009. The measurements were performed in four post-cardiac surgery sedated adults in post-surgical intensive care unit and four nurses at the bedside, and at four points: scenario A, inhalation sedation without gas extraction system or contrafluran as a reference scenario; scenario B, applying a gas extraction system to the ventilator; scenario C, using contrafluran; and scenario 0, performing intravenous isolation sedation. Sevoflurane concentrations were measured in the nurses’ breathing area during patient care, and at 1.5 and 8 m from the ventilator using diffusive passive monitor badges. Results: All badges corresponding to the nurses’ breathing area were below 2 ppm. Levels of sevoflurane detected using prevention systems were lower than that in the control situation. Only one determination over 2 ppm was found, corresponding to the monitor placed nearest the gas outlet of the ventilator in scenario A. Trace concentrations of sevoflurane were found in scenario 0 during intravenous sedation. Conclusions: Administration of sevoflurane through the AnaConDa® system during inhalation sedation in post-surgical intensive care units is safe for healthcare workers, but gas extraction systems or scavenging systems, such as CONTRAfluran™ should be used to reduce occupational exposure as much as possible (AU)


Introducción y objetivo: La exposición ocupacional al sevoflurano no debe exceder de 2 ppm. Durante la sedación por inhalación con sevoflurano utilizando el dispositivo anestésico conservación ( AnaConDa ®) en la unidad de cuidados post-anestésicos , gases residuales se pueden reducir mediante sistemas de extracción de gases o dispositivos de barrido como CONTRAfluran ™ . Sin embargo , la eficacia de estos métodos no se ha establecido claramente. Para determinar el escenario más seguro para los trabajadores de la salud durante la sedación por inhalación con sevoflurano en la unidad de cuidados intensivos post- quirúrgica. Materiales y métodos: Un estudio experimental sobre la exposición laboral se llevó a cabo en una unidad de cuidados post- cardiotorácica entre marzo y agosto de 2009. Las mediciones se realizaron cada cuatro adultos sedados después de cirugía cardiaca en la unidad de cuidados intensivos post- quirúrgica y cuatro enfermeras en el lado de la cama , y en cuatro puntos : el escenario A , sedación por inhalación sin sistema de extracción de gas o contrafluran como un escenario de referencia ; escenario B, la aplicación de un sistema de extracción de gas al ventilador ; escenario C , utilizando contrafluran y escenario 0 , realizando intravenosa sedación aislamiento. Concentraciones de sevoflurano fueron medidas en la zona de respiración de las enfermeras durante el cuidado del paciente, y en el 1,5 y 8 m desde el ventilador utilizando difusivos insignias monitor pasivo. Resultados Todas las insignias correspondientes a la zona de respiración de las enfermeras estaban por debajo de 2 ppm. Los niveles de sevoflurano detectado utilizando sistemas de prevención fueron más bajos que en la situación de control. Sólo se encontró un empeño superior a 2 ppm, correspondiente al monitor colocado más cerca de la salida de gas del ventilador en el escenario A concentraciones traza de sevoflurano fueron encontrados en el escenario 0 durante la sedación intravenosa. Conclusiones: La administración de sevoflurano a través del sistema AnaConDa ® durante la sedación por inhalación en las unidades de cuidados intensivos postquirúrgicos es seguro para los trabajadores de la salud, pero los sistemas de extracción de gas o sistemas de evacuación, tales como CONTRAfluran ™ debe ser usado para reducir la exposición ocupacional tanto como sea posible (AU)


Subject(s)
Humans , Occupational Exposure/analysis , Inhalation Exposure/analysis , Anesthetics/adverse effects , Health Personnel , Administration, Inhalation , Risk Factors
3.
Rev Esp Anestesiol Reanim ; 61(3): 133-9, 2014 Mar.
Article in English | MEDLINE | ID: mdl-24439525

ABSTRACT

INTRODUCTION AND OBJECTIVE: Occupational exposure to sevoflurane should not exceed 2 ppm. During inhalation sedation with sevoflurane using the anaesthetic conserving device (AnaConDa(®)) in the post-anaesthesia care unit, waste gases can be reduced by gas extraction systems or scavenging devices such as CONTRAfluran™. However, the efficacy of these methods has not been clearly established. To determine the safest scenario for healthcare workers during inhalation sedation with sevoflurane in the post-surgical intensive care unit. MATERIALS AND METHODS: An experimental study on occupational exposure was conducted in a post-cardiothoracic care unit during March-August 2009. The measurements were performed in four post-cardiac surgery sedated adults in post-surgical intensive care unit and four nurses at the bedside, and at four points: scenario A, inhalation sedation without gas extraction system or contrafluran as a reference scenario; scenario B, applying a gas extraction system to the ventilator; scenario C, using contrafluran; and scenario 0, performing intravenous isolation sedation. Sevoflurane concentrations were measured in the nurses' breathing area during patient care, and at 1.5 and 8 m from the ventilator using diffusive passive monitor badges. RESULTS: All badges corresponding to the nurses' breathing area were below 2 ppm. Levels of sevoflurane detected using prevention systems were lower than that in the control situation. Only one determination over 2 ppm was found, corresponding to the monitor placed nearest the gas outlet of the ventilator in scenario A. Trace concentrations of sevoflurane were found in scenario 0 during intravenous sedation. CONCLUSIONS: Administration of sevoflurane through the AnaConDa(®) system during inhalation sedation in post-surgical intensive care units is safe for healthcare workers, but gas extraction systems or scavenging systems, such as CONTRAfluran™ should be used to reduce occupational exposure as much as possible.


Subject(s)
Air Pollutants, Occupational/adverse effects , Anesthesia, Inhalation/instrumentation , Anesthetics, Inhalation/adverse effects , Gas Scavengers , Hypnotics and Sedatives/adverse effects , Intensive Care Units , Methyl Ethers/adverse effects , Nurses , Occupational Exposure , Air Pollutants, Occupational/analysis , Anesthetics, Inhalation/administration & dosage , Equipment Design , Gases , Humans , Hypnotics and Sedatives/administration & dosage , Hypnotics and Sedatives/analysis , Inhalation Exposure/adverse effects , Inhalation Exposure/analysis , Methyl Ethers/analysis , Recovery Room , Sevoflurane , Ventilators, Mechanical
6.
Rev Esp Anestesiol Reanim ; 38(4): 265-7, 1991.
Article in Spanish | MEDLINE | ID: mdl-1771289

ABSTRACT

Transoesophageal echocardiography is a new technique that allows continuous and noninvasive assessment of cardiac function during surgery. More recently this technique is being used to detect the presence of external objects into the cardiac cavities. We report a case of Swan-Ganz catheter knotting confirmed by this echocardiography technique. He was a 57 year old male with previous history of arterial hypertension and ischemic heart disease who was scheduled for surgery because poor response to medical therapy. After anesthetic induction a thermodilution catheter was introduced percutaneously into the right internal jugular vein under continuous pressure monitoring from the distal catheter hole. In view of the difficulties in introducing the catheter into the pulmonary artery an intravascular catheter knotting was suspected and a bidimensional transesophageal echocardiogram confirmed the diagnosis. During extracorporeal circulation the catheter was withdrawn through a right auriculotomy. Monitoring with a Swan-Ganz catheter, as other invasive monitoring techniques, is followed by a certain degree of complications which should be avoided by a careful manipulation. Echocardiography is a valuable diagnostic procedure to identify the position of monitoring catheters into the cardiac cavities.


Subject(s)
Catheterization, Swan-Ganz/adverse effects , Echocardiography/methods , Monitoring, Intraoperative , Heart Atria/surgery , Humans , Internal Mammary-Coronary Artery Anastomosis , Male , Middle Aged
7.
Rev Esp Anestesiol Reanim ; 38(3): 167-9, 1991.
Article in Spanish | MEDLINE | ID: mdl-1961961

ABSTRACT

Classically, the cardiac output is measured by the thermodilution method, employing a standard volume of 5% D/W at 4 degrees C. Recently, however, a room-temperature (17-24 degrees C) measurements have been used, in such a way that a lower gradient between the injectate and the patient temperature is established. This lact could question the sensitivity and reliability of the technique evaluated. We have studied 20 patients undergoing different operations, in whom the cardiac output was measured by injecting a standard volume of 5 ml 5% D/W at room-temperature or at 5 degrees C, randomly assigned, in order to evaluate any difference between the two techniques. Over a total of 100 cardiac output determinations taken in normothermic conditions (19-24 degrees C) the mean was 4.24 +/- 1.13 l/min (means +/- SD). In hypothermic conditions the cardiac output was 4.28 +/- 1.14 l/min (means +/- SD). Results showed no statistical difference between both methods.


Subject(s)
Cardiac Output , Temperature , Thermodilution/methods , Aged , Evaluation Studies as Topic , Humans , Middle Aged , Monitoring, Intraoperative , Postoperative Care , Prospective Studies , Random Allocation
8.
Rev Esp Anestesiol Reanim ; 38(1): 48-50, 1991.
Article in Spanish | MEDLINE | ID: mdl-2057628

ABSTRACT

We report the clinical case of a 56 years old male suffering dystrophic ampullar epidermolysis. He underwent brachial plexus blockade to remove a right hand tumor. The patient presented bilateral pseudosyndactylia, flexion retraction of the left hand, and erosive lesions in the inferior extremities, forearm, and trunk interfered monitorization and venous catheterization. Cutaneous friction or trauma should be carefully avoided since in this patient might produce detachment of the epidermis and subsequent ampullar formation. Cutaneous electrodes without adhesive components, padded sphygmomanometers, ear pulsimeter, and venous catheter sutured to the skin were used during monitorization. Anesthetic management of patients with dystrophic ampullar epidermolysis should consider careful airway manipulation, reduction of mucocutaneous contacts, prevention of pressure or friction skin trauma, appropriate electrolyte and plasma volume reposition, and use of nonadhesive material. To avoid airway manipulation regional anesthesia should be considered in patients with ampullar epidermolysis. We recommend regional anesthesia with ketamine.


Subject(s)
Anesthesia , Epidermolysis Bullosa Dystrophica , Brachial Plexus , Epidermolysis Bullosa Dystrophica/surgery , Humans , Male , Middle Aged , Nerve Block
SELECTION OF CITATIONS
SEARCH DETAIL
...