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1.
J Cardiothorac Vasc Anesth ; 31(4): 1335-1340, 2017 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-28800989

RESUMEN

OBJECTIVE: To compare the standard intraluminal approach with the placement of the 9-French Arndt endobronchial blocker with an extraluminal approach by measuring the time to positioning and other relevant intraoperative and postoperative parameters. DESIGN: A prospective, randomized, controlled trial. SETTING: University hospital. PARTICIPANTS: The study comprised 41 patients (20 intraluminal, 21 extraluminal) undergoing thoracic surgery. INTERVENTION: Placement of a 9-French Arndt bronchial blocker either intraluminally or extraluminally. Comparisons between the 2 groups included the following: (1) time for initial placement, (2) quality of isolation at 1-hour intervals during one-lung ventilation, (3) number of repositionings during one-lung ventilation, and (4) presence or absence of a sore throat on postoperative days 1 and 2 and, if present, its severity. MEASUREMENTS AND MAIN RESULTS: Median time to placement (min:sec) in the extraluminal group was statistically faster at 2:42 compared with 6:24 in the intraluminal group (p < 0.05). Overall quality of isolation was similar between groups, even though a significant number of blockers in both groups required repositioning (extraluminal 47%, intraluminal 40%, p > 0.05), and 1 blocker ultimately had to be replaced intraoperatively. No differences in the incidence or severity of sore throat postoperatively were observed. CONCLUSIONS: A statistically significant reduction in time to placement using the extraluminal approach without any differences in the rate of postoperative sore throat was observed. Whether placed intraluminally or extraluminally, a significant percentage of Arndt endobronchial blockers required at least one intraoperative repositioning.


Asunto(s)
Bronquios/cirugía , Broncoscopía/instrumentación , Intubación Intratraqueal/instrumentación , Ventilación Unipulmonar/instrumentación , Toracoscopía/instrumentación , Adulto , Anciano , Anciano de 80 o más Años , Broncoscopía/efectos adversos , Broncoscopía/métodos , Femenino , Humanos , Intubación Intratraqueal/efectos adversos , Intubación Intratraqueal/métodos , Masculino , Persona de Mediana Edad , Ventilación Unipulmonar/efectos adversos , Ventilación Unipulmonar/métodos , Faringitis/diagnóstico , Faringitis/etiología , Estudios Prospectivos , Distribución Aleatoria , Toracoscopía/efectos adversos , Toracoscopía/métodos
2.
J Clin Sleep Med ; 20(5): 783-792, 2024 May 01.
Artículo en Inglés | MEDLINE | ID: mdl-38174855

RESUMEN

STUDY OBJECTIVES: The association of in-hospital medical emergency team activation (META) among patients with atrial fibrillation (AF) at risk for obstructive sleep apnea (OSA) is unclear. This study evaluates the performance of the DOISNORE50 sleep questionnaire as an OSA screener for patients with AF and determines the prevalence of META among perioperative patients with underlying AF who have a diagnosis or are at risk for OSA. METHODS: A prospective perioperative cohort of 2,926 patients with the diagnosis of AF was assessed for DOISNORE50 questionnaire screening. Propensity-score matching was used to match patients' physical characteristics, comorbidities, length of stay, and inpatient continuous positive airway pressure device usage. META and intensive care unit admissions during the surgical encounter, 30-day hospital readmissions, and 30-day emergency department visits were evaluated. RESULTS: A total of 1,509 out of 2,926 AF patients completed the DOISNORE50 questionnaire and were enrolled in the OSA safety protocol. Following propensity-score matching, there were reduced adjusted odds of META in the screened group of 0.69 (95% confidence interval: 0.48-0.98, P < .001) in comparison to the unscreened group. The adjusted odds of intensive care unit admissions and emergency department visits within 30 days of discharge were statistically lower for the screened group compared with the unscreened group. CONCLUSIONS: Among perioperative AF patients, evidence supports DOISNORE50 screening and implementation of an OSA safety protocol for reduction of META. This study identified decreased odds of META, intensive care unit admissions, and emergency department visits among the screened group. The high-risk and known OSA group showed reduced odds of META following the implementation of an OSA safety protocol. CITATION: Saha AK, Sheehan KN, Xiang KR, et al. Preoperative sleep apnea screening protocol reduces medical emergency team activation in patients with atrial fibrillation. J Clin Sleep Med. 2024;20(5):783-792.


Asunto(s)
Fibrilación Atrial , Cuidados Preoperatorios , Apnea Obstructiva del Sueño , Humanos , Fibrilación Atrial/diagnóstico , Femenino , Masculino , Estudios Prospectivos , Anciano , Encuestas y Cuestionarios , Apnea Obstructiva del Sueño/diagnóstico , Cuidados Preoperatorios/métodos , Cuidados Preoperatorios/estadística & datos numéricos , Persona de Mediana Edad , Tamizaje Masivo/métodos , Tamizaje Masivo/estadística & datos numéricos , Puntaje de Propensión
3.
J Am Med Dir Assoc ; 20(10): 1340-1343.e2, 2019 10.
Artículo en Inglés | MEDLINE | ID: mdl-31201101

RESUMEN

Patients with obstructive sleep apnea (OSA) have increased postoperative complications that are important for patient safety and healthcare utilization. Questionnaires help identify patients at risk for OSA; however, among older adults who preoperatively self-administered OSA questionnaires, the frequency of postoperative Medical Emergency Team Activation (META), rapid response, code blue, code stroke, is unknown. OBJECTIVES: Identify whether having OSA questionnaires completed by patients is feasible in the preoperative clinic. Determine the frequency of META among older patients at risk for OSA. DESIGN AND INTERVENTION: Cohort of prospective patients independently completed 2 OSA questionnaires in a preoperative clinic, STOP-Bang (SB) and ISNORED (IS). Observers blinded to questionnaire responses recorded incidence of META. SETTING AND PARTICIPANTS: Of the 898 consecutive patients approached in the preoperative assessment clinic and surgical navigation center, 575 (64%) consented and completed the questionnaires in <5 minutes and were included in the analysis. MEASURES: Sleep questionnaire responses and frequency of inpatient postoperative META. RESULTS: With an affirmative response to ≥3 questions on either questionnaire, 65% of patients enrolled were at risk for OSA. Of these, 3.1% sustained an META. In patients at risk for OSA, META occurred in 7.6% (SB+) and 7.2% (IS+) vs 2.5% (SB+) and 1.7% (IS+) for low risk. METAs were disproportionately higher among patients aged ≥65 years (6.3% vs 1.7%; P < .018), American Society of Anesthesiologists (ASA) physical status class ≥3, and IS+. All patients with META positively answered ≥3 of 15 components of the 2 questionnaires. CONCLUSIONS/IMPLICATIONS: Preoperative, self-administration of SB and IS questionnaires is feasible. Overall, 65% of those with affirmative responses to ≥3 questions were at risk for OSA and associated with a disproportionate number of postoperative META in older patients. Additionally, risk of OSA identified by preoperative sleep questionnaires was associated with postoperative META among older adults. Use of clinical tools and OSA questionnaires may improve preoperative identification of META in this population.


Asunto(s)
Servicio de Urgencia en Hospital , Grupo de Atención al Paciente , Cuidados Preoperatorios , Sueño , Encuestas y Cuestionarios , Estudios de Factibilidad , Femenino , Humanos , Masculino , Estudios Prospectivos , Apnea Obstructiva del Sueño
4.
Anesthesiol Clin ; 36(4): 493-507, 2018 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-30390774

RESUMEN

Obtaining routine preoperative laboratory tests increases health care costs and has been listed, by the Choosing Wisely Campaign, as one of the top 5 practices anesthesiologists should avoid. Routine testing without clinical indication is not cost-effective and could cause harm and unnecessary delays. Abnormal findings are more likely to be false positive and costly to pursue, introduce new risks, and increase anxiety for the patient. Preoperative testing need to be performed only following a targeted history and physical examination, factoring severity of surgery, and comorbidities such that the benefit of the test outweighs risk.


Asunto(s)
Técnicas de Laboratorio Clínico/métodos , Cuidados Preoperatorios/métodos , Humanos
5.
Reg Anesth Pain Med ; 42(4): 432-436, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-28492441

RESUMEN

Currently, the American Society of Regional Anesthesia and Pain Medicine (ASRA) anticoagulation guidelines recommend that before the performance of a neuraxial procedure a minimum of 24 hours should elapse following a treatment dose of enoxaparin (1 mg/kg twice daily or 1.5 mg/kg once daily). The guidelines have since their inception also consistently recommended against the routine use of anti-Xa level monitoring for patients receiving enoxaparin. However, we noted in our clinical practice that anti-Xa levels were frequently still elevated despite patients meeting the time-based recommendation for treatment dose enoxaparin. To further investigate the possibility that residual anticoagulant activity may persist longer than 24 hours after a treatment dose of enoxaparin, we assessed anti-Xa level activity in patients presenting for elective surgery. Despite nearly universal compliance with ASRA's anticoagulation guidelines (1 sample was drawn at 23.25 hours), anti-Xa activity was found to be elevated in 11 of 19 patients. While 10 patients had an anti-Xa level within the peak prophylactic range (0.2-0.5 IU/mL), 1 patient's level was found to still be in the peak therapeutic range (0.5-1.0 IU/mL). These findings suggest that significant anticoagulant activity may persist longer than previously appreciated after the last treatment dose of enoxaparin and that the current time-based ASRA recommendation may not be conservative enough. Further research is needed to delineate the level of anti-Xa activity below which it is likely safe to proceed with a neuraxial procedure, but it may be time to reconsider the utility of anti-Xa level monitoring when it is available.


Asunto(s)
Anestesia de Conducción/normas , Anticoagulantes/sangre , Enoxaparina/sangre , Inhibidores del Factor Xa/sangre , Manejo del Dolor/normas , Sociedades Médicas/normas , Adolescente , Anciano , Anciano de 80 o más Años , Anestesia de Conducción/métodos , Anticoagulantes/administración & dosificación , Coagulación Sanguínea/efectos de los fármacos , Coagulación Sanguínea/fisiología , Enoxaparina/administración & dosificación , Femenino , Humanos , Masculino , Persona de Mediana Edad , Manejo del Dolor/métodos , Guías de Práctica Clínica como Asunto/normas , Factores de Tiempo , Estados Unidos/epidemiología
6.
J Am Geriatr Soc ; 65(9): 2023-2028, 2017 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-28470836

RESUMEN

OBJECTIVES: To determine how often outpatient physician visits detect sleep apnea (SA) in older persons in the United States. DESIGN: Retrospective Analysis. SETTING: US non hospital and hospital based clinics. PARTICIPANTS: US physicians. MEASUREMENTS: National Ambulatory Medical Care Survey and National Hospital Ambulatory Medical Care Survey data from 1993 to 2011 were used to assess the frequency of physicians' coding diagnoses of SA in persons aged 65 and older. Which specialties are most likely to report SA, the most-common comorbid conditions reported with SA, and the likelihood of reporting SA in patient visits for dementia and preoperative care were assessed. RESULTS: From 1993 to 2011, physicians reported SA in 0.3% of all office visits in persons aged 65 and older. SA reported in visits increased from 130,000 in 1993 to 2,070,000 in 2011, with an annual per capita visit reporting rate of 0.07% to 0.74%. In older populations, the proportion of documented SA visits by specialists rose, and that of primary care providers decreased. Older adults with a diagnosis of SA had higher average number of comorbidities than those without SA (1.8 vs 1.3). Reporting SA was low in visits with a diagnosis of dementia and classified as a preoperative visits. CONCLUSION: In two nationwide surveys, SA reporting by physicians in elderly adults was 16 as greater in 2001 as in 1993, although reporting of SA remains infrequent (<1% of visits) even in vulnerable populations.


Asunto(s)
Envejecimiento , Médicos de Atención Primaria/estadística & datos numéricos , Síndromes de la Apnea del Sueño/diagnóstico , Anciano , Anciano de 80 o más Años , Humanos , Estudios Retrospectivos , Especialización/estadística & datos numéricos , Estados Unidos
8.
Biol Reprod ; 67(3): 995-1002, 2002 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-12193413

RESUMEN

Hypoxia-inducible factor 1 (HIF-1) is a transcription factor composed of alpha and beta subunits. Stabilized from proteasome degradation and activated by hypoxia, HIF-1 stimulates expression of hypoxia-sensitive genes that mediate oxygen homeostasis in many tissues. Our hypothesis is that HIF-1 is involved in the cellular response to hypoxia in the ischemic testis. Goals of this study were to determine if HIF-1alpha mRNA is expressed in the testis, epididymis, and accessory sex glands of adult Sprague-Dawley rats and to determine if HIF-1alpha mRNA and protein expression in the testis is affected by experimentally induced ischemia. Total RNA from reproductive organs of adult rats was analyzed by relative reverse transcription-polymerase chain reaction (RT-PCR) analysis. HIF-1alpha mRNA showed equal expression in testis, all segments of epididymis, ductus deferens, accessory sex glands, and penis. To examine the effects of ischemia on HIF-1alpha mRNA and protein expression in the testis, rats were subjected to unilateral testicular ischemia by placing a ligature around spermatic artery or ischemia-inducing experimental torsion and reperfusion. RT-PCR revealed that HIF-1alpha mRNA expression at all times of ischemic treatment and reperfusion was unchanged compared with normoxic controls. HIF-1alpha protein was detected by immunoblot analysis of nuclear protein extracts from normoxic testes. Steady-state levels of HIF-1alpha protein were stimulated by 15 min of ischemia and showed a 2-fold increase at 30 min and 1, 3, and 6 h. HIF-1alpha protein was also elevated by experimental torsion and reperfusion compared with normoxic controls. These results support the hypothesis that HIF-1 may play a role in the cellular response to hypoxia in the ischemic testis.


Asunto(s)
Isquemia/metabolismo , ARN Mensajero/análisis , Testículo/irrigación sanguínea , Factores de Transcripción/genética , Factores de Transcripción/metabolismo , Animales , Epidídimo/química , Expresión Génica , Subunidad alfa del Factor 1 Inducible por Hipoxia , Cinética , Masculino , Pene/química , Fosforilación , Ratas , Ratas Sprague-Dawley , Daño por Reperfusión/metabolismo , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Torsión del Cordón Espermático/metabolismo , Testículo/química , Factores de Transcripción/análisis , Conducto Deferente/química
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