11 results on '"Antonio, Esquinas"'
Search Results
2. Noninvasive positive-pressure ventilation to treat hypercapnic coma secondary to respiratory failure.
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Díaz GG, Alcaraz AC, Talavera JC, Pérez PJ, Rodriguez AE, Cordoba FG, and Hill NS
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- APACHE, Acute Disease, Aged, Coma mortality, Contraindications, Female, Glasgow Coma Scale, Hospital Mortality, Humans, Male, Respiratory Insufficiency etiology, Respiratory Insufficiency mortality, Survival Rate, Treatment Failure, Treatment Outcome, Coma complications, Hypercapnia complications, Positive-Pressure Respiration adverse effects, Positive-Pressure Respiration instrumentation, Positive-Pressure Respiration methods, Respiratory Insufficiency therapy
- Abstract
Introduction: Hypercapnic coma secondary to acute respiratory failure (ARF) is considered to be a contraindication to the use of treatment with noninvasive positive-pressure ventilation (NPPV). However, intubation exposes these patients to the risk of complications such as nosocomial pneumonia, sepsis, and even death., Patients and Methods: We performed a prospective, open, noncontrolled study to assess the outcomes of NPPV therapy in patients with a Glasgow coma scale (GCS) score of = 8 points due to ARF. The primary goal of the study was to determine the success of NPPV therapy (defined as a response to therapy allowing the patient to avoid endotracheal intubation, and to survive a stay in the ICU and at least 24 h on a medical ward) in patients with hypercapnic coma, compared to those who started NPPV therapy while awake. The secondary goal of the study was to identify the variables that can predict a failure of NPPV therapy in these patients., Results: A total of 76 coma patients (80%) responded to NPPV therapy, and 605 patients with GCS scores > 8 responded to therapy (70%; p = 0.04). A total of 25 coma patients died in the hospital (26.3%), and 287 noncoma patients died in the hospital (33.2%; p = 0.17). The variables related to the success of NPPV therapy were GCS score 1 h posttherapy (odds ratio [OR], 2.32; 95% confidence interval [CI], 1.53 to 3.53) and higher levels of multiorgan dysfunction, as measured by the maximum sequential organ failure assessment index score reached during NPPV therapy (OR, 0.72; 95% CI, 0.55 to 0.92)., Conclusions: We concluded that selected patients with hypercapnic coma secondary to ARF can be treated as successfully with NPPV as awake patients with ARF.
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- 2005
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3. Outcome of patients with acute heart failure secondary to acute myocardial infarction treated with noninvasive mechanical ventilation
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Domingo A. Pascual-Figal, Andrés Carrillo-Alcaraz, Antonia López-Martínez, Víctor Martínez-Pérez, Luna Carrillo-Alemán, Juan Miguel Sánchez-Nieto, Antonio Esquinas-Rodríguez, Nuria Alonso-Fernández, Ana Renedo-Villarroya, and Miguel Guia
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Acute coronary syndrome ,medicine.medical_treatment ,Myocardial Infarction ,030204 cardiovascular system & hematology ,law.invention ,03 medical and health sciences ,0302 clinical medicine ,law ,medicine ,Humans ,Hospital Mortality ,Prospective Studies ,Myocardial infarction ,Prospective cohort study ,Heart Failure ,Mechanical ventilation ,Noninvasive Ventilation ,business.industry ,General Medicine ,medicine.disease ,Respiration, Artificial ,Intensive care unit ,Clinical trial ,Anesthesia ,Heart failure ,Etiology ,Respiratory Insufficiency ,business - Abstract
Introduction and objectives Noninvasive ventilation (NIV) has been shown to reduce the rate of endotracheal intubation and mortality in patients with acute heart failure (AHF). However, patients with AHF secondary to acute coronary syndrome/acute myocardial infarction (ACS-AMI) have been excluded from many clinical trials. The purpose of this study was to compare the effectiveness of NIV between patients with AHF triggered by ACS-AMI and by other etiologies. Methods Prospective cohort study of all patients with AHF treated with NIV admitted to the intensive care unit for a period of 20 years. Patients were divided according to whether they had ACS-AMI as the cause of the AHF episode. NIV failure was defined as the need for endotracheal intubation or death. Results A total of 1009 patients were analyzed, 403 (40%) showed ACS-AMI and 606 (60%) other etiologies. NIV failure occurred in 61 (15.1%) in the ACS-AMI group and in 64 (10.6%) in the other group (P = .031), without differences in in-hospital mortality (16.6% and 14.9%, respectively; P = .478). Conclusions The presence of ACS-AMI as the triggering cause of AHF did not influence patients with acute respiratory failure requiring noninvasive respiratory support .
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- 2022
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4. Face-mask noninvasive ventilation plus high flow nasal oxygen in COVID-19 patients: 'one size fits all' or tailored approach?
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Francesco ALESSANDRI, Giovanni GIORDANO, and Antonio ESQUINAS
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humans ,masks ,oxygen ,oxygen inhalation therapy ,respiration, artificial ,COVID-19 ,noninvasive ventilation ,respiratory insufficiency ,Anesthesiology and Pain Medicine ,artificial ,respiration - Published
- 2022
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5. To: Epistaxis as a complication of high-flow nasal cannula therapy in adults
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Abhijit Nair and Antonio Esquinas
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Epistaxis ,Oxygen Inhalation Therapy ,Humans ,Cannula ,General Medicine ,Critical Care and Intensive Care Medicine ,Respiratory Insufficiency - Published
- 2022
6. High-Flow Nasal Cannula in COVID-19 Pneumonia: Practical Issues
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Andres Laserna, Julian E. Barahona-Correa, Peter Papadakos, and Antonio Esquinas
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Noninvasive Ventilation ,SARS-CoV-2 ,Oxygen Inhalation Therapy ,COVID-19 ,Cannula ,Humans ,Critical Care and Intensive Care Medicine ,Respiratory Insufficiency - Published
- 2022
7. Non-invasive mechanical ventilation with average volume-assured pressure support. Results according to the aetiology of acute respiratory failure
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Killen Harold Briones Claudett, Antonio Esquinas Rodriguez, Mónica H. Briones Claudett, Miguel Puga Tejada, Mariuxi del Pilar Cabrera Bańos, Jorge Daher N., Byron Bermeo, and Michelle Grunauer
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Respiratory Distress Syndrome ,Anesthesiology and Pain Medicine ,Noninvasive Ventilation ,Original and Clinical Articles ,Continuous Positive Airway Pressure ,Humans ,General Medicine ,Prospective Studies ,Critical Care and Intensive Care Medicine ,Respiratory Insufficiency ,Respiration, Artificial - Abstract
Background: Until now, the ventilatory strategy with BiPAP S/T plus average volume-assured pressure support (AVAPS) has not been evaluated for its use in the different types of acute respiratory failure (ARF). Consequently we report the results of the use of this ventilatory strategy in these clinical scenarios. Methods: This is a single-centre prospective study. The subjects were categorised according to the type of ARF: (1) hypercapnic ARF: chronic obstructive pulmonary disease and bronchial asthma; and (2) hypoxaemic ARF: pneumonia, acute respiratory distress syndrome, congestive heart failure, and interstitial lung disease. Multiple logistic regression was used to determine predictors of non-invasive mechanical ventilation (NIV) failure (intubation). Further, in a subgroup of patients with de novo hypoxaemic ARF, analysis of variances with repeated measures was used to determine factors associated with NIV outcome. Results: Sixty-eight subjects were included in this study. The NIV success rate was 69.1% and the mortality rate was 20.6%. A multivariate analysis showed that the number of affected lung quadrants on chest X-ray (OR: 4.23, 95% CI: 4.17–4.31; P < 0.001) and ARF precipitating disease (OR: 4.46, 95% CI: 4.43–4.51; P < 0.001) were determinants of NIV failure. In the hypoxaemic ARF subgroup (n = 58), significant differences in several parameters were found between patients with positive and negative outcomes. Conclusions: The use of BiPAP S/T – AVAPS in subjects with hypercapnic ARF is associated with a better outcome than in those with de novo hypoxaemic ARF. Trial register: ISRCTN96455367.
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- 2022
8. Noninvasive ventilation: Education and training. A narrative analysis and an international consensus document
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Habib Karim, Karen Burns, Laura Ciobanu, Mohamad El-Khatib, Antonello Nicolini, Nicola Vargas, Thierry Hernández-Gilsoul, Szymon Skoczyński, Vito Falcone, Jean-Michel Arnal, John Bach, Luca De Santo, Alberto Lucchini, Joerg Steier, Andrea Purro, Angelo Petroianni, Catherine Sassoon, Stefano Bambi, Margarida Aguiar, Ayman Soubani, Corinne Taniguchi, Corrado Mollica, David Berlin, Edoardo Piervincenzi, Fabrizio Rao, Ferini-Strambi Luigi, Rodolfo Ferrari, Giancarlo Garuti, Gerhard Laier-Groeneveld, Giuseppe Fiorentino, Kwok Ho, Jaber Alqahtani, Manuel Luján, Onnen Moerer, Onofrio Resta, Paola Pierucci, Peter Papadakos, Stephan Steiner, Sven Stieglitz, Yalim Dikmen, Jun Duan, Pradipta Bhakta, Alejandro Iglesias, Nadia Corcione, Vânia Caldeira, Zuhal Karakurt, Gabriele Valli, Eumorfia Kondili, Maria Ruggieri, Margarida Raposo, Fabrizio Bottino, Rafael Soler-González, Mohan Gurjar, José Sandoval-Gutierrez, Behrouz Jafari, Marta Arroyo-Cozar, Ana Noval, Igor Barjaktarevic, Irena Sarc, Bushra Mina, Zbigniew Szkulmowski, Antonio Esquinas, Reazaul Karim, H. M., Burns, K. E. A., Ciobanu, L. D., El-Khatib, M., Nicolini, A., Vargas, N., Hernandez-Gilsoul, T., Skoczynski, S., Falcone, V. A., Arnal, J. -M., Bach, J., De Santo, L. S., Lucchini, A., Steier, J., Purro, A., Petroianni, A., Sassoon, C. S., Bambi, S., Aguiar, M., Soubani, A. O., Taniguchi, C., Mollica, C., Berlin, D. A., Piervincenzi, E., Rao, F., Luigi, F. -S., Ferrari, R., Garuti, G., Laier-Groeneveld, G., Fiorentino, G., Ho, K. M., Alqahtani, J. S., Lujan, M., Moerer, O., Resta, O., Pierucci, P., Papadakos, P., Steiner, S., Stieglitz, S., Dikmen, Y., Duan, J., Bhakta, P., Iglesias, A. U., Corcione, N., Caldeira, V., Karakurt, Z., Valli, G., Kondili, E., Ruggieri, M. P., Raposo, M. S., Bottino, F., Soler-Gonzalez, R., Gurjar, M., Sandoval-Gutierrez, J. L., Jafari, B., Arroyo-Cozar, M., Noval, A. R., Barjaktarevic, I., Sarc, I., Mina, B., Szkulmowski, Z., Esquinas, A. M., Karim, H, Burns, K, Ciobanu, L, El-Khatib, M, Nicolini, A, Vargas, N, Hernández-Gilsoul, T, Skoczyński, S, Falcone, V, Arnal, J, Bach, J, De Santo, L, Lucchini, A, Steier, J, Purro, A, Petroianni, A, Sassoon, C, Bambi, S, Aguiar, M, Soubani, A, Taniguchi, C, Mollica, C, Berlin, D, Piervincenzi, E, Rao, F, Luigi, F, Ferrari, R, Garuti, G, Laier-Groeneveld, G, Fiorentino, G, Ho, K, Alqahtani, J, Luján, M, Moerer, O, Resta, O, Pierucci, P, Papadakos, P, Steiner, S, Stieglitz, S, Dikmen, Y, Duan, J, Bhakta, P, Iglesias, A, Corcione, N, Caldeira, V, Karakurt, Z, Valli, G, Kondili, E, Ruggieri, M, Raposo, M, Bottino, F, Soler-González, R, Gurjar, M, Sandoval-Gutierrez, J, Jafari, B, Arroyo-Cozar, M, Noval, A, and Esquinas, A
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Pulmonary and Respiratory Medicine ,osebje ,usposabljanje ,Attitude of Health Personnel ,education ,MEDLINE ,Developing country ,HSM PNEU ,Narrative inquiry ,staff ,zdravstveno osebje -- izobraževanje ,Education ,noninvasive ventilation -- education ,Medical Staff, Hospital ,Humans ,Training ,Narrative ,health personnel -- education ,udc:616.2 ,Respiratory Distress Syndrome ,Medical education ,Noninvasive Ventilation ,training ,Program ,Staff ,neinvazivna ventilacija -- izobraževanje ,Pneumonia, Ventilator-Associated ,3. Good health ,Clinical trial ,Systematic review ,Life support ,Programs ,Clinical Competence ,Respiratory Insufficiency ,Psychology ,Developed country ,Noninvasive ventilation - Abstract
Noninvasive ventilation (NIV) is an increasingly used method of respiratory support. The use of NIV is expanding over the time and if properly applied, it can save patients' lives and improve long-term prognosis. However, both knowledge and skills of its proper use as life support are paramount. This systematic review aimed to assess the importance of NIV education and training. Literature search was conducted (MEDLINE: 1990 to June, 2018) to identify randomized controlled studies and systematic reviews with the results analyzed by a team of experts across the world through e-mail based communications. Clinical trials examining the impact of education and training in NIV as the primary objective was not found. A few studies with indirect evidence, a simulation-based training study, and narrative reviews were identified. Currently organized training in NIV is implemented only in a few developed countries. Due to a lack of high-grade experimental evidence, an international consensus on NIV education and training based on opinions from 64 experts across the twenty-one different countries of the world was formulated. Education and training have the potential to increase knowledge and skills of the clinical staff who deliver medical care using NIV. There is a genuine need to develop structured, organized NIV education and training programs, especially for the developing countries. info:eu-repo/semantics/publishedVersion
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- 2019
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9. Use of noninvasive mechanical ventilation with pressure support guaranteed with average volume in de novo hypoxaemic respiratory failure. A pilot study
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Michelle Grunauer, Carlos Israel Torres Herrera, Christian Roberto Pazmiño Dueñas, Killen H. Briones-Claudett, Mariuxi del Pilar Cabrera Baños, Miguel Puga-Tejada, Mónica H. Briones-Claudett, and Antonio Esquinas Rodriguez
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Adult ,Male ,ARDS ,medicine.medical_treatment ,Pilot Projects ,Critical Care and Intensive Care Medicine ,law.invention ,03 medical and health sciences ,0302 clinical medicine ,law ,medicine ,Tidal Volume ,Intubation ,Humans ,030212 general & internal medicine ,Prospective Studies ,Prospective cohort study ,Hypoxia ,Aged ,Mechanical ventilation ,Aged, 80 and over ,COPD ,Noninvasive Ventilation ,business.industry ,General Medicine ,Middle Aged ,medicine.disease ,Intensive care unit ,Anesthesiology and Pain Medicine ,030228 respiratory system ,Respiratory failure ,Heart failure ,Anesthesia ,Female ,business ,Respiratory Insufficiency - Abstract
This study was designed to determine the results associated with the use of noninvasive mechanical ventilation (NIV) using the BiPAP S/T-AVAPS ventilation strategy in subjects with mild to moderate de novohypoxaemicrespiratory failure.This is a prospective study that includes subjects with de novohypoxaemic respiratory failure (not produced by acute exacerbations of COPD, chronic lung disease, or congestive heart failure) with mild to moderate PaO₂/FiO₂, who were admitted to the Intensive Care Unit (ICU) of Santa Maria Clinic in Guayaquil, Ecuador. Subjects were divided into two groups and compared according to their PaO₂/FiO₂: higher than 100 and up to 200 mm Hg (moderate ARDS) or between 200 and 300 mm Hg (mild ARDS) (both groups were ventilated with the BiPAP S/T-AVAPS strategy). A value of P0.05 was considered significant.A total of 38 subjects were analysed in this study. The total rate of intubation was 34.2% while the mortality rate was 28.9%. Significant differences were observed when comparing success versus failure in exhaled tidal volumes (P = 0.04), peak inspired pressure (P0.001), PaO₂ (P0.001), SaO₂ (P0.002), PaO₂/FiO₂ (P0.002), RR (P0.001), HR (P0.001), and inspiratory time (P = 0.029) measured at baseline and at 12-hour, 24-hour and 48-hour intervals.The BiPAP S/T-AVAPS ventilatory mode can be used in subjects with de novo hypoxaemic respiratory failure with special vigilance concerning exhaled tidal volumes and inspired pressure.
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- 2018
10. New arguments for NIV efficacy in the treatment of acute respiratory failure from the ovarian hyperstimulation syndrome
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Laura, Ciobanu, Antonio, Esquinas, and Daniela, Boisteanu
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Adult ,Ovarian Hyperstimulation Syndrome ,Noninvasive Ventilation ,Treatment Outcome ,Humans ,Female ,Emergencies ,Respiratory Insufficiency - Published
- 2018
11. Noninvasive mechanical ventilation with average volume assured pressure support (AVAPS) in patients with chronic obstructive pulmonary disease and hypercapnic encephalopathy.
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Briones Claudett, Killen Harold, Claudett, Monica Briones, Miguel Chung Sang Wong, Martinez, Alberto Nuques, Espinoza, Ricardo Soto, Montalvo, Mayra, Rodriguez, Antonio Esquinas, Diaz, Gumersindo Gonzalez, and Andrade, Michelle Grunauer
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LUNG diseases ,RESPIRATORY insufficiency ,CHRONIC diseases ,PHYSICAL diagnosis ,PHYSICIANS - Abstract
Background: Non-invasive mechanical ventilation (NIV) in patients with acute respiratory failure has been traditionally determined based on clinical assessment and changes in blood gases, with NIV support pressures manually adjusted by an operator. Bilevel positive airway pressure-spontaneous/timed (BiPAP S/T) with average volume assured pressure support (AVAPS) uses a fixed tidal volume that automatically adjusts to a patient's needs. Our study assessed the use of BiPAP S/T with AVAPS in patients with chronic obstructive pulmonary disease (COPD) and hypercapnic encephalopathy as compared to BiPAP S/T alone, upon immediate arrival in the Emergency-ICU. Methods: We carried out a prospective interventional match-controlled study in Guayaquil, Ecuador. A total of 22 patients were analyzed. Eleven with COPD exacerbations and hypercapnic encephalopathy with a Glasgow Coma Scale (GCS) <10 and a pH of 7.25-7.35 were assigned to receive NIV via BiPAP S/T with AVAPS. Eleven patients were selected as paired controls for the initial group by physicians who were unfamiliar with our study, and these patients were administered BiPAP S/T. Arterial blood gases, GCS, vital signs, and ventilatory parameters were then measured and compared between the two groups. Results: We observed statistically significant differences in favor of the BiPAP S/T + AVAPS group in GCS (P = .00001), pCO
2 (P = .03) and maximum inspiratory positive airway pressure (IPAP) (P = .005), among others. However, no significant differences in terms of length of stay or days on NIV were observed. Conclusions: BiPAP S/T with AVAPS facilitates rapid recovery of consciousness when compared to traditional BiPAP S/T in patients with chronic obstructive pulmonary disease and hypercapnic encephalopathy. [ABSTRACT FROM AUTHOR]- Published
- 2013
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