Cognitive Training to Reduce Memory Disturbance Associated With Postoperative Cognitive Impairment After Elective Noncardiac Surgery: An Experimental Study.

PURPOSE: Assess the efficiency of a cognitive training program using an artificial intelligence application to optimize cognitive reserve and reduce memory disturbance in patients aged 55 to 75 after Class II-III elective noncardiac surgery. DESIGN: Experimental with random assignment. METHODS: The study was conducted on 80 patients undergoing surgery at the Teknon Medical Center Hospital in Barcelona, from April 2018 to June 2021. Both groups were evaluated with cognitive tests before surgery and 7 and 30 days after surgery. The experimental group was subjected to cognitive training for 10 days before surgery to improve their cognitive reserve. FINDINGS: Significant differences were found between the study groups 30 days after surgery in the three screening tests (Mini-Cog, T@M, and MFE). The intervention group presented with fewer cognitive and memory alterations. Age and pre-existing comorbidities were not correlated with an impact on memory impairment or cognitive function. CONCLUSIONS: A cognitive training program based on artificial intelligence, prescribed and monitored by anesthesia nurses has a positive impact on increasing cognitive reserve and reducing memory disturbance in patients aged 55 to 75 undergoing Class II to III elective, noncardiac surgery. This intervention may serve as a prehabilitation strategy in patients with a risk of cognitive dysfunction evaluated by anesthesia nurses for the purpose of preserving their cognitive function and optimizing their recovery.

Fiabilidad del control de presión del neumotaponamiento del tubo endotraqueal por el método de palpación digital en el Centro Médico Teknon / Reliability of palpation-based endotracheal cuff pressure assessment in Centro Médico Teknon

Introducción:La presión del neumotaponamiento no es estrictamente controlada durante las intervenciones quirúrgicas. La medición objetiva se reemplaza por la medición mediante dígito-palpación, inexacta y con tendencia a la hiperinsuflación. Ésta genera complicaciones postoperatorias (dolor, tos y ronquera). El objetivo del estudio es evaluar la fiabilidad del inflado del neumotaponamiento por digito-palpación realizado por personal experto. Material y métodos:Se realizó un estudio descriptivo transversal en pacientes operados electivamente en nuestro centro bajo anestesia general e intubación endotraqueal, entre octubre y diciembre de 2020. Se incluyeron 138 pacientes. Se registraron parámetros biométricos y el inflado del neumotaponamiento por dígito-palpación de personal experto, y se comparó con medición por manómetro para ajuste siempre a una presión estandarizada (30 cm H2O). Se midió con manómetro la presión al final del procedimiento, y se analizó su variación respecto a la inicial y su relación con posición quirúrgica, duración de intervención y diámetro del tubo endotraqueal. Resultados:La distribución de la presión inicial medida por manómetro muestra tendencia al sobreinflado de la estimación por dígito-palpación, con coeficiente de correlación kappa de 0,6. La variable presión final por manómetro muestra tendencia a la pérdida de presión respecto a la inicial estandarizada. No se encuentra relación estadísticamente significativa entre presión final por manómetro y posición quirúrgica, tamaño de tubo o tiempo quirúrgico (aunque en cirugías de más de 3 horas la presión final es claramente inferior al resto). (AU)

Introduction:Endotracheal cuff pressure is not routinely controlled during surgical interventions. Objective measurements are replaced by palpation-based estimations which are inexact and tending to hyperinsuflation. This causes postoperative complications (throat pain, coughing and hoarseness). The aim of this study is evaluating the reliability of endotracheal cuff pressure assessed by palpation of expertise clinicians. Materials and methods:A transversal descriptive study was performed in patients electively operated under general anaesthesia and endotracheal intubation in our hospital between October and December 2020. 138 patients were included. Biometric parameters and cuff palpation-based pressure were registered. It was compared to manometer-based pressure measurement and adjusted in all cases to a standardized pressure (30 cm H2O). Final procedure pressure was also measured with manometer, and its relationship with initial pressure and surgical position, intervention length and endotracheal tube diameter was analysed. Results:Initial manometer-based pressure measurement shows palpation-based measurement tends to hyperinsuflation, with a 0,6 kappa correlation coefficient. Manometer-based final cuff pressure shows tendency to decrease when compared to initial standardised pressure. No statistically significant relationship was found between final cuff pressure and surgical position, tube diameter or intervention length (even though interventions above 3 hours show significantly inferior final pressure values). (AU)

Opioid-free anesthesia for patients with joint hypermobility syndrome undergoing craneo-cervical fixation: a case-series study focused on anti-hyperalgesic approach.

BACKGROUND: Patients with Ehlers-Danlos Syndrome/Hypermobility Type (EDS-HT/JHS) and Craneo-Cervical Instability frequently suffer from severe widespread pain which is difficult to control. Chronic neuroinflammation, opioid-induced hyperalgesia, and central sensitization may explain this painful condition. The aim of this study was to determine if opioid-free anesthesia plus the postoperative administration of lidocaine, ketamine and dexmedetomidine can reduce postoperative pain and the need of methadone rescues in comparison with opioid-based management in these patients undergoing Craneo-Cervical Fixation (CCF). The secondary aim was to assess the needs of opioids at hospital-discharge, incidence of gastrointestinal complications and the requirement of anxiolytic. METHODS: A retrospective, consecutive case series study was designed. 42 patients with EDS-HT/JHS undergoing CCF were enrolled in two groups: an OFA-plus Group that received opioid-free anesthesia with propofol, lidocaine, ketamine and dexmedetomidine, and OP Group, opioid-based anesthesia-analgesia. The main variables: Preoperative Visual Analogue Score (VAS), postoperative VAS on the 1st, 2nd, 4th and 6th days, sufentanil or morphine requirements, need for methadone rescue, and VAS at hospital-discharge. Data was presented by mean ± SD, percentage, median or interquartile range. Chi-squared or Fisher's test. 95% C.I and P values < 0.05. RESULTS: Nineteen patients in OFA-plus, and 23 patients in OP group. VAS was lower in OFA-plus on the postoperative days evaluated (p < 0.001).VAS at hospital-discharge was lower in OFA-plus: 4.96 (4.54-5.37) vs. OP 6.39 (6.07-6.71) (p < 0.001). Methadone requirement was lower in the OFA-plus (p < 0.001). 78% of patients in OFA-plus didn't need methadone rescue. 95% in OP group needed methadone rescues at high doses(> 15 mg/day). No differences regarding equivalent doses of sufentanil or morphine consumption on the 2nd, 4th, and 6th postoperative days were found. OFA-plus decreased ileus, nausea and vomiting (p < 0.001). 60.9% in OFA-plus group decreased opioid requirements at hospital-discharge compared with preoperative values. A 77% reduction of anxiolytics requirements was shown. CONCLUSION: OFA-plus management for patients undergoing CCF with EDS-HT/JHS shows significant reduction in postoperative pain and at hospital-discharge compared with opioid-based anesthesia. OFA-plus management decreases the total doses of methadone rescues, reduces anxiolytic requirements and gastrointestinal side-effects, except for constipation. OFA-plus management is a feasible option to improve postoperative pain control, reducing the opioids' use and their postoperative side-effects in patients undergoing CCF with EDS-HT/JHS.