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1.
BMC Anesthesiol ; 24(1): 166, 2024 May 03.
Artículo en Inglés | MEDLINE | ID: mdl-38702641

RESUMEN

BACKGROUND: Pregnancy is associated with an increased risk of pulmonary aspiration during general anaesthesia, but the incidence of this complication is not well defined. METHODS: We performed a retrospective database review in a tertiary care university hospital to determine the incidence of pulmonary aspiration in pregnant patients undergoing endotracheal intubation, with and without Rapid Sequence Induction (RSI), as well as face-mask ventilation and supraglottic airway devices. We included Patients in the 2nd or 3rd trimester of pregnancy and immediate postpartum undergoing surgical procedures. The primary endpoint was the occurrence of pulmonary aspiration. RESULTS: Data from 2,390 patients undergoing general anaesthesia for cerclage of cervix uteri, manual removal of retained placenta, repair of obstetric laceration, or postpartum bleeding were retrospectively evaluated. A supraglottic airway device or face-mask ventilation was used in 1,425/2,390 (60%) of patients, while 638/2,390 (27%) were intubated. RSI was used in 522/638 (82%) of patients undergoing tracheal intubation, or 522/2,390 (22%) of the entire cohort. In-depth review of the charts, including 54 patients who had been initially classified as "possible pulmonary aspiration" by anaesthetists, revealed that this adverse event did not occur in the cohort. CONCLUSIONS: In conclusion, in this obstetric surgery patient population at risk for pulmonary aspiration, supraglottic airway devices were used in approximately 60% of cases. Yet, no aspiration event was detected with either a supraglottic airway or endotracheal intubation.


Asunto(s)
Manejo de la Vía Aérea , Hospitales Universitarios , Intubación Intratraqueal , Aspiración Respiratoria , Humanos , Femenino , Estudios Retrospectivos , Embarazo , Adulto , Manejo de la Vía Aérea/métodos , Intubación Intratraqueal/métodos , Aspiración Respiratoria/prevención & control , Aspiración Respiratoria/etiología , Periodo Posparto , Centros de Atención Terciaria , Anestesia General/métodos
2.
Acta Clin Croat ; 62(Suppl1): 105-112, 2023 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-38746610

RESUMEN

Aspiration and ingestion of a foreign body is most frequently seen in children younger than 3 years. Foreign body aspiration is always a life-threatening, urgent state demanding quick recognition and treatment to avoid potentially lethal complications. Most foreign bodies that are ingested pass spontaneously through the gastrointestinal tract without complications, however, some could lead to problems if they become lodged. A literature review was performed via MEDLINE database using key terms. Primary care providers should be trained to give proper initial care. Aspirated/ingested foreign bodies in children removed by rigid or flexible bronchoscopy/gastroscopy always are challenging procedures that require well-planned anesthesia management and excellent intercommunication between anesthesiologists and surgeons. Extracorporeal membrane oxygenation can be used as a rescue mode of support in children with life-threatening foreign body aspiration for stabilization before, during and after removal of the aspirated foreign body. It is of utmost importance that all foreign body extractions, if possible, be done in centers supplied with all the necessary equipment and trained personnel. However, prevention of foreign body aspiration and ingestion is still the best therapy.


Asunto(s)
Cuerpos Extraños , Preescolar , Humanos , Lactante , Broncoscopía , Cuerpos Extraños/terapia , Aspiración Respiratoria/etiología , Aspiración Respiratoria/prevención & control , Aspiración Respiratoria/terapia , Recién Nacido
3.
BMC Anesthesiol ; 21(1): 254, 2021 10 26.
Artículo en Inglés | MEDLINE | ID: mdl-34702191

RESUMEN

BACKGROUND: Despite well-defined recommendations, prolonged fasting times for clear fluids and solids are still common before elective surgery in adults. Extended fasting times may lead to discomfort, thirst, hunger and physiological dysfunctions. Previous studies have shown that prolonged fasting times are frequently caused by patients being misinformed as well as inadequate implementation of the current guidelines by medical staff. This study aimed to explore how long elective surgery patients fast in a German secondary care hospital before and after the introduction of an educational note for patients and re-training for the medical staff. METHODS: A total of 1002 patients were enrolled in this prospective, non-randomised interventional study. According to the power calculation, in the first part of the study actual fasting times for clear fluids and solids were documented in 502 consecutive patients, verbally instructed as usual regarding the recommended fasting times for clear fluids (2 h) and solids (6 h). Subsequently, we implemented additionally to the verbal instruction a written educational note for the patients, including the recommended fasting times. Furthermore, the medical staff was re-trained regarding the fasting times using emails, newsletters and employee meetings. Thereafter, another 500 patients were included in the study. We hypothesised, that after these quality improvement procedures, actual fasting times for clear fluids and solids would be more accurate on time. RESULTS: Actual fasting times for clear fluids were in the median 11.3 (interquartile range 6.8-14.3; range 1.5-25.5) h pre-intervention, and were significantly reduced to 5.0 (3.0-7.2; 1.5-19.8) h after the intervention (median difference (95%CI) - 5.5 (- 6.0 to - 5.0) h). The actual fasting times for solids also decreased significantly, but only from 14.5 (12.1-17.2; 5.4-48.0) h to 14.0 (12.0-16.3; 5.4-32.0) h after the interventions (median difference (95%CI) - 0.52 (- 1.0 to - 0.07) h). CONCLUSIONS: The study showed considerably extended actual fasting times in elective adult surgical patients, which were significantly reduced by simple educational/training interventions. However, the actual fasting times still remained considerably longer than defined in recommended guidelines, meaning further process optimisations like obligatory fluid intake in the early morning are necessary to improve patient comfort and safety in future. TRIAL REGISTRATION: German registry of clinical studies (DRKS-ID: DRKS 00020530 , retrospectively registered).


Asunto(s)
Ayuno , Cooperación del Paciente , Educación del Paciente como Asunto , Cuidados Preoperatorios , Mejoramiento de la Calidad , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Anestesia General , Procedimientos Quirúrgicos Electivos , Femenino , Humanos , Masculino , Persona de Mediana Edad , Estudios Prospectivos , Aspiración Respiratoria/prevención & control , Adulto Joven
4.
Acta Otolaryngol ; 141(9): 851-856, 2021 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-34459710

RESUMEN

BACKGROUND: Posterior hypopharyngeal carcinoma indicates a poor prognosis. Previous treatments predicted negative influence to the pronunciation and swallowing function. The present study focuses on improving survival rate while improving quality of life. AIM: To investigate on the surgical techniques of the preservation of laryngeal function of posterior hypopharyngeal carcinoma. METHODS: Eighteen patients with posterior hypopharyngeal carcinoma of T2-T3 were studied. All primary lesions were removed and the defects were repaired with the radial forearm free flap (RFFF). RESULTS: The 3-year overall survival rate was 51.9%. All patients could maintain daily caloric intake by feeding orally, and remove the gastric tube 28-61 days after operation. Assessed swallowing function by Fiberoptic endoscopic evaluations of swallowing. When eating solid food, 66.67% patients had food residue; no food entered airway, and all patients had Penetration-Aspiration Scale of level 1. As for liquid, 11.11% patients had level 5, 16.67% level 4, 27.78% level 2 and 44.44% level 1. CONCLUSIONS: By preserving the integrity of larynx and superior laryngeal nerve with repairing the defects of posterior wall of hypopharynx with RFFF, patients with T2 and T3 stage posterior hypopharyngeal carcinoma could live a better quality of life.


Asunto(s)
Carcinoma de Células Escamosas/cirugía , Neoplasias Hipofaríngeas/cirugía , Colgajos Quirúrgicos , Carcinoma de Células Escamosas/mortalidad , Carcinoma de Células Escamosas/patología , Carcinoma de Células Escamosas/terapia , Quimioradioterapia Adyuvante , Deglución , Trastornos de Deglución/etiología , Humanos , Neoplasias Hipofaríngeas/mortalidad , Neoplasias Hipofaríngeas/patología , Neoplasias Hipofaríngeas/terapia , Nervios Laríngeos , Laringe , Masculino , Persona de Mediana Edad , Estadificación de Neoplasias , Complicaciones Posoperatorias/prevención & control , Calidad de Vida , Aspiración Respiratoria/prevención & control , Tasa de Supervivencia
5.
Muscle Nerve ; 62(6): 681-687, 2020 12.
Artículo en Inglés | MEDLINE | ID: mdl-32737993

RESUMEN

BACKGROUND: Nephropathic cystinosis is a lysosomal storage disorder with late-onset systemic complications, such as myopathy and dysphagia. Currently employed outcome measures lack sensitivity and responsiveness for dysphagia and myopathy, a limitation to clinical trial readiness. METHODS: We evaluated 20 patients with nephropathic cystinosis in two visits over the course of a year to identify outcomes sensitive to detect changes over time. Patients also underwent an expiratory muscle strength training program to assess any effects on aspiration and dysphagia. RESULTS: There were significant differences in the Timed Up and Go Test (TUG) and Timed 25-Foot Walk (25-FW) between baseline and 1-y follow-up (P < .05). Maximum expiratory pressure (MEP) and peak cough flow (PCF) significantly improved following respiratory training (P < .05). CONCLUSIONS: Improved respiratory outcomes may enhance patients ability to expel aspirated material from the airway, stave off pulmonary sequelae associated with chronic aspiration, and yield an overall improvement in physical health and well-being.


Asunto(s)
Cistinosis/fisiopatología , Trastornos de Deglución/fisiopatología , Enfermedades Musculares/fisiopatología , Adulto , Ejercicios Respiratorios/métodos , Ensayos Clínicos como Asunto , Trastornos de Deglución/rehabilitación , Miopatías Distales/fisiopatología , Miopatías Distales/rehabilitación , Femenino , Fuerza de la Mano , Humanos , Masculino , Presiones Respiratorias Máximas , Persona de Mediana Edad , Fuerza Muscular , Enfermedades Musculares/rehabilitación , Evaluación de Resultado en la Atención de Salud , Medición de Resultados Informados por el Paciente , Rendimiento Físico Funcional , Aspiración Respiratoria/prevención & control , Prueba de Paso , Adulto Joven
6.
Curr Opin Otolaryngol Head Neck Surg ; 28(3): 145-154, 2020 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-32332203

RESUMEN

PURPOSE OF REVIEW: The use of commercially or naturally thickened liquids is a well-established treatment for patients with dysphagia to fluids, the aim of which is to improve swallow safety by minimizing risk of aspiration. Although the most recent systematic reviews conclude that this treatment lacks evidential support and leads to patient-reported worsening health and quality of life, thickened liquids continue to be used with patients with dysphagia across clinical settings. This review briefly summarizes the evidence and considers potential reasons for the apparent mismatch between the evidence and clinical practice. RECENT FINDINGS: Continuing practice with thickened liquids is influenced by a range of factors, including gaps in clinical knowledge, inadequate patient involvement, a culture of common practice and a reliance on invalid surrogate studies or research lacking a credible association between thickened liquids and clinically meaningful endpoints. SUMMARY: While awaiting further research, clinical decision-making about thickened liquids can be improved by considering the evidence of clinically meaningful endpoints, promoting shared decision-making with patients and underpinning practice with knowledge about the complex relationship between dysphagia, aspiration and pneumonia.


Asunto(s)
Trastornos de Deglución/terapia , Soluciones/administración & dosificación , Administración Oral , Toma de Decisiones Clínicas , Deglución/fisiología , Trastornos de Deglución/complicaciones , Trastornos de Deglución/fisiopatología , Humanos , Aspiración Respiratoria/etiología , Aspiración Respiratoria/prevención & control , Soluciones/química , Viscosidad
7.
Curr Opin Anaesthesiol ; 33(3): 277-283, 2020 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-32324656

RESUMEN

PURPOSE OF REVIEW: This review focuses on the use of point-of-care ultrasound (PoCUS) in the obstetric context for airway management and assessment of aspiration risk, the placement of neuraxial blocks and the diagnosis and follow-up of cardiorespiratory dysfunction. RECENT FINDINGS: Gastric ultrasound is a useful aspiration risk assessment tool in pregnant patients. Total gastric fluid assessment models and specific cut-offs between high-risk and low-risk stomachs are presented. Airway assessment is useful to detect specific changes in pregnancy and to guide airway management. Handheld ultrasound devices with automated neuraxial landmark detection capabilities could facilitate needle placement in the future. Lung and cardiac ultrasonography is useful in the management of preeclampsia, pulmonary arterial hypertension and peripartum cardiomyopathy. SUMMARY: Owing to its noninvasiveness, ease of accessibility and lack of exposure to radiation, PoCUS plays an increasing and essential role in aspiration risk assessment, airway management, neuraxial anaesthesia and cardiorespiratory diagnosis and decision-making during pregnancy.


Asunto(s)
Manejo de la Vía Aérea/métodos , Contenido Digestivo/diagnóstico por imagen , Sistemas de Atención de Punto , Aspiración Respiratoria/prevención & control , Ultrasonografía/métodos , Ecocardiografía/métodos , Femenino , Humanos , Embarazo , Medición de Riesgo/métodos , Estómago/diagnóstico por imagen
8.
Einstein (Sao Paulo) ; 18: eAO4952, 2020.
Artículo en Inglés, Portugués | MEDLINE | ID: mdl-31939524

RESUMEN

OBJECTIVE: To define physician´s behavior in the face of a mentally capable elderly dysphagic patients at risk of pulmonary aspiration, who do not accept oral restriction. METHODS: Observational, cross-sectional study, presenting a clinical case of an independent elderly with clinical complaints of dysphagia and laryngotracheal aspiration by flexible endoscopic evaluation of swallowing who rejected the proposal to restrict oral diet. A questionnaire about the patient's decision-making process was used to assess whether the physician was sympathetic and justify their answer, and if they are aware of hierarchy of ethical principles (recognition of the person´s value, autonomy, beneficence, nonmaleficence and justice), in the decision-making process, and which was the main principle that guided their decision. RESULTS: One hundred participants were classified by time since graduation as Group I (less than 10 years) and Group II (more than 10 years). Of them, 60% agreed with the patient's decision, with no difference between the groups. The main reason was autonomy of patients, in both groups. Among those who were not sympathetic, the main argument was beneficence and nonmaleficence, considering the risk between benefit and harm. As to awareness about the hierarchy of principles, we did not find differences between the groups. Autonomy was the principle that guided those who were sympathetic with the patient's decision, and justice among those who didnot agree. CONCLUSION: Physicians were sympathetic with the patient's decision regarding autonomy, despite the balance between risks of beneficence and nonmaleficence, including death. We propose to formalize a non-compliance term.


Asunto(s)
Trastornos de Deglución/complicaciones , Pautas de la Práctica en Medicina/estadística & datos numéricos , Aspiración Respiratoria/etiología , Negativa del Paciente al Tratamiento/estadística & datos numéricos , Anciano de 80 o más Años , Toma de Decisiones Clínicas , Estudios Transversales , Trastornos de Deglución/prevención & control , Gastroscopía/métodos , Gastrostomía/métodos , Humanos , Intubación Gastrointestinal/métodos , Masculino , Autonomía Personal , Relaciones Médico-Paciente , Aspiración Respiratoria/prevención & control , Factores de Riesgo , Encuestas y Cuestionarios , Factores de Tiempo
9.
J Voice ; 34(1): 121-126, 2020 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-30340927

RESUMEN

Vocal fold movement impairment may significantly compromise postoperative recovery and quality of life of patients following thoracic or cardiothoracic surgery or prolonged intubation. The literature is limited and there is no standard screening protocol for the optimal postoperative swallowing and aspiration evaluations. We performed retrospective review of adult patients undergoing early vocal fold (VF) injection laryngoplasty for acute postoperative Vocal fold movement impairment (<30 days) that had both pre- and postinjection speech language pathologist (SLP) performed swallowing/aspiration evaluations. Records were reviewed for demographics, clinical characteristics, procedural details, and short-term outcome measures of oral intake. In total, 30 patients were included, and had data on swallowing/aspiration studies before and after the VF injection laryngoplasty. Most of the patients were injected within 5 days following the laryngologist evaluation and within 14 days following the iatrogenic recurrent laryngeal nerve injury (23/30, 76.7%). The majority of patients were injected at the bedside by awake transcutaneous injection (22/30, 73.3%), six patients were injected in the operating room under general anesthesia, and two at the outpatient clinic. Pre- and postinjection SLP evaluations included clinical bedside assessment or instrumental evaluation. Following VF injection laryngoplasty, oral diet advancement was noted in 81.8% of the patients that were nil per os before the injection (18/22). No complications were noted. In conclusions, acute VFMI following surgery requires immediate diagnosis and therapeutic strategy to minimize postoperative complications and to overcome impairments in the voice, swallow, and cough. Otolaryngology-SLP interdisciplinary aspiration and swallowing assessment protocol is proposed based on our experience and an extensive literature review.


Asunto(s)
Trastornos de Deglución/prevención & control , Deglución , Laringoplastia , Complicaciones Posoperatorias/cirugía , Traumatismos del Nervio Laríngeo Recurrente/cirugía , Aspiración Respiratoria/prevención & control , Trastornos de la Voz/cirugía , Calidad de la Voz , Adulto , Anciano , Anciano de 80 o más Años , Trastornos de Deglución/diagnóstico , Trastornos de Deglución/etiología , Trastornos de Deglución/fisiopatología , Femenino , Humanos , Enfermedad Iatrogénica , Masculino , Persona de Mediana Edad , Complicaciones Posoperatorias/diagnóstico , Complicaciones Posoperatorias/etiología , Complicaciones Posoperatorias/fisiopatología , Recuperación de la Función , Traumatismos del Nervio Laríngeo Recurrente/diagnóstico , Traumatismos del Nervio Laríngeo Recurrente/etiología , Traumatismos del Nervio Laríngeo Recurrente/fisiopatología , Aspiración Respiratoria/diagnóstico , Aspiración Respiratoria/etiología , Aspiración Respiratoria/fisiopatología , Estudios Retrospectivos , Factores de Riesgo , Factores de Tiempo , Resultado del Tratamiento , Trastornos de la Voz/diagnóstico , Trastornos de la Voz/etiología , Trastornos de la Voz/fisiopatología , Adulto Joven
10.
Einstein (Säo Paulo) ; 18: eAO4952, 2020. tab, graf
Artículo en Inglés | LILACS | ID: biblio-1056063

RESUMEN

ABSTRACT Objective: To define physician´s behavior in the face of a mentally capable elderly dysphagic patients at risk of pulmonary aspiration, who do not accept oral restriction. Methods: Observational, cross-sectional study, presenting a clinical case of an independent elderly with clinical complaints of dysphagia and laryngotracheal aspiration by flexible endoscopic evaluation of swallowing who rejected the proposal to restrict oral diet. A questionnaire about the patient's decision-making process was used to assess whether the physician was sympathetic and justify their answer, and if they are aware of hierarchy of ethical principles (recognition of the person´s value, autonomy, beneficence, nonmaleficence and justice), in the decision-making process, and which was the main principle that guided their decision. Results: One hundred participants were classified by time since graduation as Group I (less than 10 years) and Group II (more than 10 years). Of them, 60% agreed with the patient's decision, with no difference between the groups. The main reason was autonomy of patients, in both groups. Among those who were not sympathetic, the main argument was beneficence and nonmaleficence, considering the risk between benefit and harm. As to awareness about the hierarchy of principles, we did not find differences between the groups. Autonomy was the principle that guided those who were sympathetic with the patient's decision, and justice among those who didnot agree. Conclusion: Physicians were sympathetic with the patient's decision regarding autonomy, despite the balance between risks of beneficence and nonmaleficence, including death. We propose to formalize a non-compliance term.


RESUMO Objetivo: Definir o comportamento médico diante de paciente idoso disfágico com risco de aspiração laringotraqueal e mentalmente capaz que não aceita a restrição da via oral. Métodos: Estudo observacional, transversal. Apresentamos um caso clínico de idoso, que vive independente, com queixas clínicas e videoendoscopia da deglutição comprovando disfagia e aspiração, que recusou a proposta de restrição da via oral. Um questionário foi aplicado sobre o processo de decisão do paciente, procurando avaliar se o médico torna-se solidário, e que justifique sua resposta, e se tem ciência da hierarquia dos princípios éticos (reconhecimento do valor da pessoa, autonomia, beneficência, não maleficência e justiça), no processo de decisão e qual o principal princípio que norteia sua decisão. Resultados: Cem participantes foram classificados por tempo de formados em Grupo I (até 10 anos) e Grupo II (mais de 10 anos). Deles 60% tornaram-se solidários à decisão do paciente, sem diferença entre os grupos. O principal argumento foi a autonomia do paciente nos dois grupos. Entre os não solidários, foi o binômio beneficência e não maleficência, e o balanço do risco/benefício e malefício. Considerando a ciência sobre a hierarquia dos princípios que regem a decisão, não encontramos diferença entre eles. A autonomia foi o principal princípio na decisão entre os solidários e a justiça entre os não solidários. Conclusão: O médico foi solidário à decisão do paciente em respeito à sua autonomia, apesar dos riscos ponderados da beneficência e da maleficência, inclusive de morte. Propomos o termo de recusa de conduta formalizada.


Asunto(s)
Humanos , Masculino , Anciano de 80 o más Años , Pautas de la Práctica en Medicina/estadística & datos numéricos , Trastornos de Deglución/complicaciones , Negativa del Paciente al Tratamiento/estadística & datos numéricos , Aspiración Respiratoria/etiología , Relaciones Médico-Paciente , Factores de Tiempo , Gastrostomía/métodos , Trastornos de Deglución/prevención & control , Estudios Transversales , Encuestas y Cuestionarios , Factores de Riesgo , Gastroscopía/métodos , Autonomía Personal , Aspiración Respiratoria/prevención & control , Toma de Decisiones Clínicas , Intubación Gastrointestinal/métodos
11.
A A Pract ; 13(12): 443-445, 2019 Dec 15.
Artículo en Inglés | MEDLINE | ID: mdl-31592830

RESUMEN

Pulmonary aspiration of gastric contents carries significant risk in children in the perioperative period. Ultrasound imaging of the gastric antrum has been validated to predict gastric content and volume in both pediatric and adult patients, and yet clinical applications in pediatric patients are sparse. We report 2 cases of children presenting for elective surgery with uncertain volume of gastric contents. Bedside gastric imaging successfully identified "full stomachs," and the information was used to direct care.


Asunto(s)
Contenido Digestivo/diagnóstico por imagen , Aspiración Respiratoria/prevención & control , Estómago/diagnóstico por imagen , Niño , Vaciamiento Gástrico , Humanos , Masculino , Periodo Perioperatorio , Ultrasonografía
12.
Otolaryngol Head Neck Surg ; 161(5): 862-869, 2019 11.
Artículo en Inglés | MEDLINE | ID: mdl-31426703

RESUMEN

OBJECTIVE: To assess the reliability and construct validity of the Penetration-Aspiration Scale in children. STUDY DESIGN: This was a retrospective cohort study of pre- and postoperative video modified barium swallow studies from children who underwent interarytenoid injection augmentation for unexplained persistent pharyngeal dysphagia. Two pediatric speech and language pathologists reviewed each study twice in a blinded and randomized fashion. SETTING: Tertiary academic pediatric hospital. SUBJECTS AND METHODS: Thirty children were identified with adequate pre- and postoperative modified barium swallow studies within 4 weeks of intervention. Children were separated into clinical outcome groups based on ability to advance to thinner diet consistencies postoperatively. Construct validity was assessed with a mixed linear model to test the hypothesis that only the clinically improved group would receive better Penetration-Aspiration Scale scores after surgery. Reliability was assessed by calculating chance-corrected agreement between raters (interrater) and raters' repeat evaluations (intrarater). RESULTS: Inter- and intrarater reliabilities (Cohen's κ) were both excellent. Results of the mixed model revealed a significant interaction between outcome group and pre- and postoperative time interval. As hypothesized, this involved a significant improvement in Penetration-Aspiration Scale score only in the improved group. CONCLUSIONS: These findings suggest that the Penetration-Aspiration Scale is a reliable and valid measure of clinical response to interarytenoid injection augmentation in children.


Asunto(s)
Cartílago Aritenoides/cirugía , Trastornos de Deglución/complicaciones , Trastornos de Deglución/cirugía , Aspiración Respiratoria/diagnóstico , Aspiración Respiratoria/prevención & control , Cartílago Aritenoides/fisiopatología , Niño , Preescolar , Trastornos de Deglución/diagnóstico , Femenino , Humanos , Lactante , Masculino , Evaluación del Resultado de la Atención al Paciente , Reproducibilidad de los Resultados , Aspiración Respiratoria/etiología , Estudios Retrospectivos
13.
Neurogastroenterol Motil ; 31(11): e13695, 2019 11.
Artículo en Inglés | MEDLINE | ID: mdl-31402571

RESUMEN

BACKGROUND: Increasing viscosity with thickening agents is a valid therapeutic strategy for oropharyngeal dysphagia (OD). To assess the therapeutic effect of a xanthan gum-based thickener (Nutilis Clear® ) at six viscosities compared with thin liquid in poststroke OD (PSOD) patients. METHODS: A total of 120 patients with PSOD were studied in this controlled, multiple-dose, fixed-order, and single-blind study using videofluoroscopy (VFSS). A series of boluses of 10 mL thin liquid and 2000, 1400, 800, 450, 250, and 150 mPa s viscosities were given in duplicate, interrupted in case of aspiration. We assessed the safety and efficacy of swallow and the kinematics of the swallow response. KEY RESULTS: A total of 41.2% patients had safe swallow at thin liquid which significantly increased for all viscosities from 71.9% at 150 mPa s to 95.6% at 1400 mPa s (P < .001). PAS score (3.7 ± 2.3) at thin liquid was also reduced by increasing bolus viscosity (P < .001). The prevalence of patients with aspiration at thin liquid was 17.5% and decreased at all viscosities (P < .01), except at 150 mPa s. Increasing viscosity shortened time to laryngeal vestibule closure (LVC) at all viscosities (P < .01) and reduced bolus velocity at ≥450 mPa s (P < .05). The prevalence of patients with pharyngeal residue at each viscosity 37.7%-44.7% was similar to that at thin liquid (41.2%). CONCLUSIONS AND INFERENCES: The prevalence of unsafe swallow with thin liquids is very high in PSOD. Increasing shear bolus viscosity with this xanthan gum-based thickener significantly increased the safety of swallow in patients with PSOD in a viscosity-dependent manner without increasing the prevalence of pharyngeal residue.


Asunto(s)
Trastornos de Deglución/etiología , Deglución/fisiología , Polisacáridos Bacterianos , Aspiración Respiratoria/prevención & control , Accidente Cerebrovascular/complicaciones , Anciano , Femenino , Humanos , Masculino , Método Simple Ciego , Viscosidad
14.
Clin Nurse Spec ; 33(5): 237-243, 2019.
Artículo en Inglés | MEDLINE | ID: mdl-31404002

RESUMEN

AIMS: The aim of this study was to decrease the number of patients with acquired aspiration mortality. DESIGN: This was an evaluation research study. Data were collected on acutely ill hospitalized patients from January 2013 to December 2017. METHODS: In 2016, a 1100-bed Midwestern quaternary care facility found an increasing trend in mortality rates of patients with acquired aspiration from 2013 to 2015. A need for improved detection of patients at risk of aspiration was identified. A multidisciplinary team analyzed this need and developed a screening process found on the American College of Chest Physicians practice guidelines and the Massey Bedside Swallowing Screen to reduce these rates. Nurses implemented the aspiration risk screening process on all hospitalized patients. Data were collected through nursing responses and chart reviews. RESULTS: Initial implementation of the aspiration risk screening process yielded procedural concerns that were ameliorated through increased education and refinement of the screen. After refinement and reimplementation, mortality data from 2016 to 2017 revealed a decrease to zero aspiration-related events. CONCLUSION: Our findings suggest implementation of a nursing-led aspiration risk screening process with acutely ill patients is a factor in decreasing patient mortality from acquired aspiration. These clinical practice changes of identifying patients at risk of aspirating and involving dysphagia therapists prior to oral intake increase patient safety while decreasing acquired aspiration mortality. IMPACT: This study addressed upward trends in patient mortality with acquired aspiration. Mortality rates declined after implementation of the aspiration risk screening process on hospitalized patients. These findings have potential to impact healthcare personnel and all acutely ill hospitalized patients.


Asunto(s)
Deglución , Tamizaje Masivo/organización & administración , Aspiración Respiratoria/prevención & control , Enfermedad Crítica , Mortalidad Hospitalaria/tendencias , Hospitalización , Humanos , Enfermeras Clínicas , Investigación en Evaluación de Enfermería , Aspiración Respiratoria/mortalidad
15.
Rev. bras. anestesiol ; 69(3): 266-271, May-June 2019. tab, graf
Artículo en Inglés | LILACS | ID: biblio-1013416

RESUMEN

Abstract Background and objectives: Pregnant women are considered patients at risk for pulmonary aspiration of gastric contents. The study aim was to evaluate the gastric antral cross-sectional area using ultrasound. Method: In this prospective study, 85 scheduled term pregnant women underwent gastric ultrasound. The outcomes were the measurement of the gastric antral cross-sectional area (main outcome), the estimated gastric volume, the incidence of pregnant women at risk for pulmonary aspiration, and the association between gastric antral cross-sectional area and clinical-demographic characteristics. Gastric antral cross-sectional area and gastric volume were compared according to body mass index <30 or ≥30. Results: The median (IIQ) for gastric antral cross-sectional area was 4 cm2 (2.8-6.3), for the estimated gastric volume it was 49.8 mL (33.7-87.2), and for the gastric volume estimated in mL.kg-1 it was 0.62 mL.kg-1 (0.39-0.95). The 95th percentile [95% confidence interval (CI)] of the gastric antral cross-sectional area and the estimated gastric volume were ≤10.3 cm2 (95% CI: 7.6-15.6) and 1.42 mL.kg-1 (95% CI: 1.20-2.64), respectively. The incidence of pregnant women at risk for pulmonary aspiration was 3.5% (CI: 3.5 (1.2-9.8)). There was a positive correlation between gastric antral cross-sectional area and weight, p < 0.001 and body mass index <0.001. Patients with a body mass index ≥30 had a gastric antral cross-sectional area and an estimated gastric volume greater than those with a body mass index <30, respectively, p < 0.01 and p < 0.02. Conclusion: Measuring the gastric antral cross-sectional area of pregnant women is feasible and easy. There was positive correlation between gastric antral cross-sectional area, body weight and body mass index. The estimation of gastric volume by measuring the gastric antral cross-sectional area can identify patients at risk for pulmonary aspiration. Obese patients had a gastric antral cross-sectional area and an estimated gastric volume greater than non-obese patients.


Resumo Justificativa e objetivos: As gestantes são consideradas pacientes de risco para aspiração pulmonar do conteúdo gástrico. O objetivo foi avaliar a área transversal do antro gástrico por meio de ultrassonografia. Método: Neste estudo prospectivo, 85 gestantes a termo agendadas foram submetidas à ultrassonografia do antro gástrico. Os desfechos foram a mensuração da área transversal do antro gástrico (desfecho principal), a estimativa do volume gástrico, a incidência de gestantes sob risco de aspiração pulmonar, a associação entre a área transversal do antro gástrico e características clínico-demográficas. A área transversal do antro gástrico e do volume gástrico foi comparada de acordo com o índice de massa corporal < 30 ou ≥ 30. Resultados: A mediana (IIQ) da área transversal do antro gástrico foi 4 cm2 (2,8-6,3), do volume gástrico estimado 49,8 mL (33,7-87,2) e do volume gástrico estimado em mL.kg-1 de 0,62 mL.kg-1 (0,39-0,95). O percentil 95 [intervalo de confiança (IC) 95%] da área transversal do antro gástrico e do volume gástrico estimado foi ≤ 10,3 cm2 (IC 95%: 7,6-15,6) e 1,42 mL.kg-1 (IC 95%: 1,20-2,64), respectivamente. A incidência de gestantes sob risco de aspiração pulmonar foi de 3,5% (IC: 3,5 (1,2-9,8). Houve correlação positiva entre a área transversal do antro gástrico e peso, p < 0,001 e índice de massa corporal p < 0,001. As pacientes com índice de massa corporal ≥ 30 apresentaram maior área transversal do antro gástrico, e do volume gástrico estimado, do que as com índice de massa corporal < 30, respectivamente p < 0,01 e p < 0,02. Conclusão: A mensuração da área transversal do antro gástrico de gestantes é factível e fácil. A área transversal do antro gástrico correlacionou-se positivamente com peso e índice de massa corporal. A estimativa do volume gástrico através da mensuração da área transversal do antro gástrico pode identificar pacientes sob risco de aspiração pulmonar. As pacientes obesas apresentaram área transversal do antro gástrico e volume gástrico estimado maior do que as não obesas.


Asunto(s)
Humanos , Femenino , Embarazo , Adulto , Adulto Joven , Antro Pilórico/diagnóstico por imagen , Estudios de Cohortes , Ultrasonografía/métodos , Aspiración Respiratoria/prevención & control , Cuidados Preoperatorios/métodos , Índice de Masa Corporal , Cesárea/métodos , Estudios Prospectivos , Contenido Digestivo/diagnóstico por imagen , Obesidad/complicaciones
16.
J Eval Clin Pract ; 25(5): 739-743, 2019 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-30548370

RESUMEN

RATIONALE AIMS AND OBJECTIVES: Pulmonary aspiration is a feared complication of anaesthesia that is associated with significant morbidity and mortality. Within the small existing body of literature on medical malpractice claims related to periprocedural aspiration, very little information is available regarding the case-specific factors that were alleged to contribute to each aspiration event. METHODS: This study searched an extensive nationwide database of medical malpractice claims and identified 43 relating to periprocedural pulmonary aspiration. RESULTS: The most common mechanism of causation cited in these claims (37%) was the failure to secure the airway with an endotracheal tube (ETT) when an elevated aspiration risk existed, most commonly because endotracheal intubation was not originally selected as part of the anaesthetic plan. The second most common alleged category of causation (33%) was the failure to perform a proper rapid-sequence induction and/or place a nasogastric tube (NGT) for decompression prior to induction. An equal amount of cases resulted in defendant versus plaintiff verdicts (44.2% each), while a settlement was reached in the remaining 11.6% of cases. CONCLUSION: These findings are generalizable to clinical practice improvement on a broader scale. They demonstrate the need to develop reliable, high-sensitivity tests for detecting elevated risk before clinicians can be expected to take special steps to protect susceptible patients, and they also show that medical malpractice can be alleged because of failure to uphold currently accepted standards of care even when the published evidence for those standards is weak. This study demonstrates that careful review of medical malpractice litigation can elucidate common contributory factors and facilitate improvements in clinical practice and decision-making.


Asunto(s)
Anestesia Endotraqueal , Intubación Intratraqueal/efectos adversos , Mala Praxis , Aspiración Respiratoria , Medición de Riesgo/normas , Procedimientos Quirúrgicos Operativos/estadística & datos numéricos , Anestesia Endotraqueal/efectos adversos , Anestesia Endotraqueal/métodos , Bases de Datos Factuales/estadística & datos numéricos , Femenino , Humanos , Revisión de Utilización de Seguros/estadística & datos numéricos , Intubación Intratraqueal/métodos , Masculino , Mala Praxis/economía , Mala Praxis/legislación & jurisprudencia , Mala Praxis/estadística & datos numéricos , Persona de Mediana Edad , Mejoramiento de la Calidad , Aspiración Respiratoria/etiología , Aspiración Respiratoria/prevención & control , Medición de Riesgo/métodos , Administración de la Seguridad/organización & administración , Administración de la Seguridad/normas , Estados Unidos
17.
Rev. chil. anest ; 48(2): 159-162, 2019.
Artículo en Español | LILACS | ID: biblio-1451722

RESUMEN

Prader-Willi syndrome (PWS) is a disorder caused by a genetic alteration that causes a multisystem clinic. It can be due mainly to three genetic mechanisms; a paternal deletion of the 15q11-13 region, a maternal uniparental disomy, or an imprinting defect. The paternal deletion is observed in 70% of the patients, the disomy in 25% and the imprinting defect in only 5% of those affected by this syndrome. 1) It is the most common syndromic cause of obesity with an estimated prevalence in the population of 1: 50,000; 2) The clinic is very variable, which is why clinical criteria have been created that, supported by the genetic study, confirm the diagnosis; 3) They have difficulty feeding during lactation, which leads to hyperphagia in childhood that leads to obesity. In the adult stage, in addition to obesity, respiratory pathology, sleep disturbances and psychological disorders stand out; 4) Objective: the aim of the present review was to compile the cases recorded in the scientific literature of patients anesthetized with PWS and the anesthetic options used in said patients.


El síndrome de Prader-Willi (SPW) es un trastorno causado por una alteración genética que provoca una clínica multisistémica. Puede ser debido principalmente a tres mecanismos genéticos; una deleción paterna de la región 15q11-13, una disomía uniparental materna o un defecto de impronta. La deleción paterna se observa en el 70% de los pacientes, la disomía en el 25% y el defecto de impronta en tan solo el 5% de los afectados por este síndrome. 1) Constituye la causa sindrómica más frecuente de obesidad con una prevalencia estimada en la población de 1:50.000; 2) La clínica es muy variable por lo que se han creado unos criterios clínicos que apoyados por el estudio genético confirman el diagnóstico; 3) Presentan dificultad para la alimentación durante la lactancia, que da paso a una hiperfagia en la infancia que deriva en obesidad. En la etapa adulta, además de la obesidad destacan la patología respiratoria, alteraciones del sueño y trastornos psicológicos; 4) Objetivo: el objetivo de la presente revisión fue recopilar los casos registrados en la literatura científica de pacientes anestesiados con SPW y las opciones anestésicas utilizadas en dichos pacientes.


Asunto(s)
Humanos , Femenino , Adulto , Síndrome de Prader-Willi/complicaciones , Anestesia de Conducción/métodos , Aspiración Respiratoria/prevención & control
18.
Ear Nose Throat J ; 97(8): 250-256, 2018 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-30138517

RESUMEN

While the impact of injection laryngoplasty on voice outcomes in unilateral vocal fold immobility has been well characterized, there is a relative paucity of literature investigating its influence on swallow function and outcomes. We performed a retrospective chart review of patients presenting to an academic cancer center between January 2014 and January 2016 to evaluate the clinical impact of percutaneous injection laryngoplasty on reduction of aspiration risk, patient perception of swallowing, and recommended safe diet in patients with vocal fold immobility after head and neck and thoracic surgery. A consecutive sample of patients diagnosed with unilateral vocal fold immobility with patient- or clinician-identified abnormal swallow function who underwent bedside or in-office vocal fold injection was included in the study. Fiberoptic endoscopic evaluation of swallowing, Eating Assessment Tool-10 scores, Functional Oral Intake Scale scores, and patient perceptual assessment of swallow were evaluated pre- and postinjection. Twenty-one patients with new-onset unilateral vocal fold immobility who underwent injection laryngoplasty were evaluated. Median Eating Assessment Tool-10 and Functional Oral Intake Scale scores postinjection were significantly improved from preinjection. Patients who initially required restricted oral diets, or were nil per os, were able to advance their diet after injection laryngoplasty. Injection laryngoplasty is a safe and effective intervention for improvement of dysphagia in patients with unilateral vocal fold immobility. A single treatment may markedly reduce or eliminate risk of aspiration and potential sequelae.


Asunto(s)
Laringoplastia/métodos , Aspiración Respiratoria/prevención & control , Parálisis de los Pliegues Vocales , Pliegues Vocales , Adulto , Anciano , Deglución/fisiología , Femenino , Humanos , Masculino , Persona de Mediana Edad , Aspiración Respiratoria/etiología , Resultado del Tratamiento , Parálisis de los Pliegues Vocales/complicaciones , Parálisis de los Pliegues Vocales/diagnóstico , Parálisis de los Pliegues Vocales/fisiopatología , Parálisis de los Pliegues Vocales/cirugía , Pliegues Vocales/patología , Pliegues Vocales/fisiopatología , Pliegues Vocales/cirugía
20.
JPEN J Parenter Enteral Nutr ; 42(5): 898-906, 2018 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-29756648

RESUMEN

BACKGROUND: Direct percutaneous endoscopic jejunostomy (DPEJ) is used for enteral nutrition (EN) in patients with postoperative anastomotic leaks after esophagectomy/gastrectomy and at high risk for aspiration. We characterized the indications, technical success, procedural/nutrition outcomes, and adverse events in a large cohort of patients undergoing DPEJ insertion. METHODS: Patients undergoing DPEJ insertion between January 2009 and March 2015 were identified from an institutional endoscopy database. Demographic, procedural, and nutrition outcome data were collected from electronic medical records. Regression analyses were used to identify predictors of adverse events and procedural success. RESULTS: A total of 452 patients underwent 480 attempts at DPEJ insertion. Indications included preoperative or postoperative weight loss (64%), postoperative upper gastrointestinal (UGI) anastomotic leak (13%), aspiration prevention (10%), and other (13%). Of attempted procedures, 398 (83%) were successful. Feeding was initiated in 389 (98%) of patients; a median of 1775 calories was delivered daily. Median body mass index (BMI) at baseline was 22.9 (11.4-44.7) and did not change over follow-up. Median change in BMI after DPEJ was similar in groups that received EN with palliative and curative intent. Adverse events following 480 attempted DPEJ insertions included 13 (3%) immediate and 74 (15%) delayed, 13 (3%) of which were serious. Patients with head and neck cancer had more adverse events than those with esophageal cancer (P = .020). CONCLUSION: DPEJ is a successful and safe procedure that effectively provides access for EN support in malnourished patients and patients with postoperative UGI cancer.


Asunto(s)
Nutrición Enteral/métodos , Yeyunostomía/métodos , Estado Nutricional , Adulto , Anciano , Anciano de 80 o más Años , Fuga Anastomótica/etiología , Fuga Anastomótica/prevención & control , Fuga Anastomótica/terapia , Estudios de Cohortes , Endoscopía Gastrointestinal/métodos , Neoplasias Esofágicas/cirugía , Esofagectomía/efectos adversos , Femenino , Gastrectomía/efectos adversos , Neoplasias de Cabeza y Cuello/cirugía , Humanos , Yeyunostomía/efectos adversos , Masculino , Desnutrición/terapia , Persona de Mediana Edad , Aspiración Respiratoria/prevención & control , Resultado del Tratamiento
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