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1.
J Robot Surg ; 18(1): 258, 2024 Jun 20.
Article de Anglais | MEDLINE | ID: mdl-38900397

RÉSUMÉ

This study examined how different goal-directed fluid therapy types affected low blood pressure and fluid infusion during robot-assisted laparoscopic gynecological surgery. They used carotid corrected flow time (FTc) and tidal volume stimulation pulse pressure variation (VtPPV) to check the patient's volume status and responsiveness. The findings indicated that various fluid therapy targets significantly influence intraoperative hypotension and fluid requirements. However, the study exclusively employed unilateral carotid ultrasound assessments, potentially overlooking physiological or pathological variations in blood flow between the left and right carotid arteries. This methodological choice raises concerns as guidelines recommend bilateral measurements for a more comprehensive evaluation. The lack of bilateral assessments could affect the study's reliability and reproducibility. Justifying the unilateral measurement approach is essential for validating clinical findings. Future research should adopt bilateral carotid ultrasound assessments or provide a detailed rationale for unilateral measurements to enhance the robustness and accuracy of clinical evaluations.


Sujet(s)
Traitement par apport liquidien , Procédures de chirurgie gynécologique , Hypotension artérielle , Laparoscopie , Interventions chirurgicales robotisées , Humains , Procédures de chirurgie gynécologique/méthodes , Laparoscopie/méthodes , Interventions chirurgicales robotisées/méthodes , Traitement par apport liquidien/méthodes , Hypotension artérielle/prévention et contrôle , Hypotension artérielle/étiologie , Femelle , Complications peropératoires/prévention et contrôle , Artères carotides/chirurgie
2.
BMC Gastroenterol ; 24(1): 203, 2024 Jun 17.
Article de Anglais | MEDLINE | ID: mdl-38886646

RÉSUMÉ

Transanal total mesorectal excision (taTME) has improved the laparoscopic dissection for rectal cancer in the narrow pelvis. Although taTME has more clinical benefits than laparoscopic surgery, such as a better view of the distal rectum and direct determination of distal resection margin, an intraoperative urethral injury could occur in excision ta-TME. This study aimed to determine the feasibility and efficacy of the ta-TME with IRIS U kit surgery. This retrospective study enrolled 10 rectal cancer patients who underwent a taTME with an IRIS U kit. The study endpoints were the safety of access (intra- or postoperative morbidity). The detectability of the IRIS U kit catheter was investigated by using a laparoscope-ICG fluorescence camera system. Their mean age was 71.4±6.4 (58-78) years; 80 were men, and 2 were women. The mean operative time was 534.6 ± 94.5 min. The coloanal anastomosis was performed in 80%, and 20% underwent abdominal peritoneal resection. Two patients encountered postoperative complications graded as Clavien-Dindo grade 2. The transanal approach with IRIS U kit assistance is feasible, safe for patients with lower rectal cancer, and may prevent intraoperative urethral injury.


Sujet(s)
Études de faisabilité , Complications postopératoires , Tumeurs du rectum , Chirurgie endoscopique transanale , Urètre , Humains , Tumeurs du rectum/chirurgie , Mâle , Femelle , Sujet âgé , Adulte d'âge moyen , Études rétrospectives , Urètre/traumatismes , Urètre/chirurgie , Chirurgie endoscopique transanale/méthodes , Chirurgie endoscopique transanale/effets indésirables , Complications postopératoires/prévention et contrôle , Complications postopératoires/étiologie , Durée opératoire , Proctectomie/méthodes , Proctectomie/effets indésirables , Complications peropératoires/prévention et contrôle , Complications peropératoires/étiologie , Rectum/chirurgie , Anastomose chirurgicale/effets indésirables , Anastomose chirurgicale/méthodes , Laparoscopie/méthodes , Laparoscopie/effets indésirables
3.
Ann Ital Chir ; 95(3): 281-283, 2024.
Article de Anglais | MEDLINE | ID: mdl-38918967

RÉSUMÉ

The most important and serious complication of thyroid surgery is recurrent laryngeal nerve (RLN) injury, and it has been noted that this risk increases considerably in the presence of anatomical variations. Double recurrent laryngeal nerve (DRLN) is very rare among RLN anatomical variations. There are only a few case reports on DRLN in the literature It is crucial to possess surgical expertise and ensure complete visualization of the nerve to minimize the likelihood of RLN injury. Intraoperative nerve monitoring (IONM) is particularly useful in identifying anatomical variations. In a 54-year-old woman undergoing diagnostic left lobectomy+isthmectomy, a left DRLN was identified during intraoperative exploration and meticulous nerve exploration with the assistance of IONM monitoring verified that the impulse conduction in both branches was identical. The surgical procedure was successfully performed without causing any harm to the nerve. Based on the case reports in the literature and our experience with this patient, we believe that surgical expertise and the utilization of IONM can decrease RLN nerve damage and reveal its anatomical variations during thyroid surgery.


Sujet(s)
Nerf laryngé récurrent , Tumeurs de la thyroïde , Thyroïdectomie , Humains , Femelle , Adulte d'âge moyen , Tumeurs de la thyroïde/chirurgie , Nerf laryngé récurrent/anatomie et histologie , Lésions du nerf laryngé récurrent/étiologie , Lésions du nerf laryngé récurrent/prévention et contrôle , Complications peropératoires/prévention et contrôle , Complications peropératoires/étiologie
4.
Int Braz J Urol ; 50(4): 489-499, 2024.
Article de Anglais | MEDLINE | ID: mdl-38701184

RÉSUMÉ

BACKGROUND: Robotic-assisted radical cystectomy (RARC) with intracorporeal urinary diversion (ICUD) is associated with significant morbidity and mortality. We present an alternative technique that preserves the complete mesenteric vascularization during the isolation of the intestinal segment used in ICUD, including distal vessels. This approach aims to minimize the risk of ischemia in both the ileal anastomosis and the isolated loop at the diversion site. METHODS: This cohort study included 31 patients, both male and female, who underwent RARC with ICUD from February 2018 to November 2023, performed by a single surgeon. Intraoperative and postoperative complications data were retrieved for analysis, employing our proposed mesentery-sparing technique in all cases. The primary endpoint was the incidence of intraoperative and postoperative complications directly attributable to the mesentery-sparing approach in ICUD. Secondary endpoints included other postoperative variables not directly related to mesentery preservation, such as the incidence of postoperative ileus requiring parenteral nutrition and the duration of hospitalization. RESULTS: None of the patients experienced intraoperative or postoperative complications directly related to mesentery-sparing, such as intestinal fistulae or internal hernias. The median duration of hospitalization was 6 days, and postoperative ileus necessitating total parenteral nutrition occurred in 19% of the patients. Minor complications (Clavien-Dindo grades I-II) accounted for 27.6% of the cases and major complications (grades III-V) accounted for 20.6%. CONCLUSION: The mesentery-sparing technique outlined herein offers an alternative method for preserving the vascularization of intestinal segments and reducing the risk of intestinal complications in ICUD during RARC.


Sujet(s)
Cystectomie , Mésentère , Complications postopératoires , Interventions chirurgicales robotisées , Dérivation urinaire , Humains , Cystectomie/méthodes , Femelle , Mâle , Interventions chirurgicales robotisées/méthodes , Dérivation urinaire/méthodes , Adulte d'âge moyen , Sujet âgé , Complications postopératoires/prévention et contrôle , Mésentère/chirurgie , Tumeurs de la vessie urinaire/chirurgie , Traitements préservant les organes/méthodes , Résultat thérapeutique , Complications peropératoires/prévention et contrôle , Études rétrospectives , Reproductibilité des résultats , Études de cohortes
5.
R I Med J (2013) ; 107(6): 19-23, 2024 Jun 03.
Article de Anglais | MEDLINE | ID: mdl-38810011

RÉSUMÉ

BACKGROUND: As resources into gynecological surgical simulation training increase, research showing an association with improved clinical outcomes is needed. OBJECTIVE: To evaluate the association between surgical simulation training for total laparoscopic hysterectomy (TLH) and rates of intraoperative vascular/visceral injury (primary outcome) and operative time. SEARCH STRATEGY: We searched Medline OVID, Embase, Web of Science, Cochrane, and CINAHL databases from the inception of each database to April 5, 2022. Selection Critera: Randomized controlled trials (RCTs) or cohort studies of any size published in English prior to April 4, 2022. DATA COLLECTION AND ANALYSIS: The summary measures were reported as relative risks (RR) or as mean differences (MD) with 95% confidence intervals using the random effects model of DerSimonian and Laird. A Higgins I2 >0% was used to identify heterogeneity. We assessed risk of bias using the Cochrane Risk of Bias tool 2.0 (for RCTs) and the Newcastle Ottawa Scale (for cohort studies). MAIN RESULTS: The primary outcome of this systematic review and meta-analysis was to evaluate the impact of simulation training on the rates of vessel/visceral injury in patients undergoing TLH. Of 989 studies screened 3 (2 cohort studies, 1 randomized controlled trial) met the eligibility criteria for analysis. There was no difference in vessel/visceral injury (OR 1.73, 95% CI 0.53-5.69, p=0.36) and operative time (MD 13.28, 95% CI -6.26 to 32.82, p=0.18) when comparing before and after simulation training. CONCLUSION: There is limited evidence that simulation improves clinical outcomes for patients undergoing TLH.


Sujet(s)
Hystérectomie , Laparoscopie , Durée opératoire , Formation par simulation , Humains , Laparoscopie/enseignement et éducation , Hystérectomie/enseignement et éducation , Hystérectomie/méthodes , Femelle , Formation par simulation/méthodes , Complications peropératoires/prévention et contrôle
6.
Vestn Oftalmol ; 140(2): 24-32, 2024.
Article de Russe | MEDLINE | ID: mdl-38742495

RÉSUMÉ

PURPOSE: This study was conducted to develop a new optimized phacoemulsification technique for Morgagnian cataract taking into account the anatomical and topographic parameters of the lens nucleus. MATERIAL AND METHODS: A working classification of Morgagnian cataract was developed based on the size of the nucleus: if the edge of the nucleus is visualized at the upper edge of the pupil or between the upper edge and the middle of the pupil, it was classified as an initial stage of Morgagnian cataract with a large nucleus; if the upper edge of the nucleus is visualized in the middle of the pupil and below, it was classified as an advanced stage of Morgagnian cataract with a small nucleus. The first group included six patients who underwent surgery using the scaffold technique with removal of the whole small nucleus into the anterior chamber. The second group included 11 patients who underwent surgery using the scaffold technique with removal of the last fragment of the nucleus into the anterior chamber. RESULTS: The use of the scaffold technique with removal of the nucleus into the anterior chamber helped reduce the number of intraoperative complications to 16.7% in the first group, compared to 27.3% in the second group, and the percentage of endothelial cell loss to 10.1% in the first group, compared to 10.7% in the second group. CONCLUSIONS: The anatomical and topographic features of the lens and the anterior segment of the eye in Morgagnian cataract with a small nucleus allow for preliminary implantation of an intraocular lens into the capsular bag to protect the posterior capsule during phacoemulsification of the nucleus with minimal mechanical, hydrodynamic and acoustic damage to the surrounding structures of the eye.


Sujet(s)
Cataracte , Phacoémulsification , Humains , Phacoémulsification/méthodes , Cataracte/complications , Mâle , Femelle , Adulte d'âge moyen , Résultat thérapeutique , Sujet âgé , Acuité visuelle , Noyau du cristallin/chirurgie , Noyau du cristallin/anatomopathologie , Complications peropératoires/prévention et contrôle , Complications peropératoires/étiologie
7.
Medicina (Kaunas) ; 60(5)2024 Apr 30.
Article de Anglais | MEDLINE | ID: mdl-38792930

RÉSUMÉ

Background and Objectives: Transurethral urologic surgeries frequently lead to hypothermia due to bladder irrigation. Prewarming in the preoperative holding area can reduce the risk of hypothermia but disrupts surgical workflow, preventing it from being of practical use. This study explored whether early intraoperative warming during induction of anesthesia, known as peri-induction warming, using a forced-air warming device combined with warmed intravenous fluid could prevent intraoperative hypothermia. Materials and Methods: Fifty patients scheduled for transurethral resection of the bladder (TURB) or prostate (TURP) were enrolled and were randomly allocated to either the peri-induction warming or control group. The peri-induction warming group underwent whole-body warming during anesthesia induction using a forced-air warming device and was administered warmed intravenous fluid during surgery. In contrast, the control group was covered with a cotton blanket during anesthesia induction and received room-temperature intravenous fluid during surgery. Core temperature was measured upon entrance to the operating room (T0), immediately after induction of anesthesia (T1), and in 10 min intervals until the end of the operation (Tend). The incidence of intraoperative hypothermia, change in core temperature (T0-Tend), core temperature drop rate (T0-Tend/[duration of anesthesia]), postoperative shivering, and postoperative thermal comfort were assessed. Results: The incidence of intraoperative hypothermia did not differ significantly between the two groups. However, the peri-induction warming group exhibited significantly less change in core temperature (0.61 ± 0.3 °C vs. 0.93 ± 0.4 °C, p = 0.002) and a slower core temperature drop rate (0.009 ± 0.005 °C/min vs. 0.013 ± 0.004 °C/min, p = 0.013) than the control group. The peri-induction warming group also reported higher thermal comfort scores (p = 0.041) and less need for postoperative warming (p = 0.034) compared to the control group. Conclusions: Brief peri-induction warming combined with warmed intravenous fluid was insufficient to prevent intraoperative hypothermia in patients undergoing urologic surgery. However, it improved patient thermal comfort and mitigated the absolute amount and rate of temperature drop.


Sujet(s)
Anesthésie générale , Hypothermie , Procédures de chirurgie urologique , Humains , Mâle , Hypothermie/prévention et contrôle , Hypothermie/étiologie , Anesthésie générale/méthodes , Sujet âgé , Adulte d'âge moyen , Femelle , Procédures de chirurgie urologique/méthodes , Complications peropératoires/prévention et contrôle
9.
World Neurosurg ; 187: e700-e706, 2024 Jul.
Article de Anglais | MEDLINE | ID: mdl-38685348

RÉSUMÉ

OBJECTIVE: A cerebellar bulge prior to posterior fossa resection is an emergency condition during surgery. Intraoperative cerebellar bulging not only increases the difficulty of lesion resection but also brings additional postoperative complications. Currently, there are few systematic reports on this topic. The predictors of cerebellar bulge and how to effectively prevent intraoperative cerebellar bulge are discussed in this article. METHODS: The clinical and imaging data of 527 patients with posterior fossa lesions who underwent resection at our hospital were retrospectively collected and analyzed. Perioperative clinical and imaging data were assessed. Variables were analyzed using univariate and multivariate regression analyses. RESULTS: Overall, 10.4% (55/527) of patients had intraoperative acute bulges. Multivariate analysis revealed that age <60 years, body mass index ≥24, lesion size ≥30 (mm), cerebellar tonsillar herniation and/or hydrocephalus, and perilesional edema (moderate-severe) were predictors of cerebellar bulging. Relief of the cerebellar bulge can be accomplished by excising the lesion, releasing cerebrospinal fluid, and removing the cerebellum (the outer one-third). Obvious cerebellar-related complications occurred in 4 patients postoperatively, and the symptoms disappeared after 6 months of follow-up. CONCLUSIONS: Cerebellar bulging during intraoperative posterior fossa resection deserves attention. Through the analysis of multiple factors related to cerebellar bulge, comprehensive evaluation and early intervention during the perioperative period are necessary. The incidence of cerebellar bulges can be reduced, and surgical complications related to cerebellar bulges can be avoided.


Sujet(s)
Cervelet , Humains , Femelle , Mâle , Adulte d'âge moyen , Études rétrospectives , Adulte , Sujet âgé , Cervelet/chirurgie , Cervelet/imagerie diagnostique , Tumeurs sous-tentorielles/chirurgie , Complications postopératoires/épidémiologie , Complications postopératoires/prévention et contrôle , Complications postopératoires/étiologie , Jeune adulte , Complications peropératoires/prévention et contrôle , Complications peropératoires/épidémiologie , Complications peropératoires/étiologie , Procédures de neurochirurgie/méthodes , Adolescent , Maladies du cervelet/chirurgie , Fosse crânienne postérieure/chirurgie , Enfant
12.
Comput Biol Med ; 174: 108395, 2024 May.
Article de Anglais | MEDLINE | ID: mdl-38599068

RÉSUMÉ

BACKGROUND: Intraoperative hypotension during cesarean section has become a serious complication for maternal and fetal healthy. It is commonly encountered by subarachnoid anesthesia. However, currently used control methods have varying degrees of side effects, such as drugs. The Root Cause Analysis (RCA) - Plan, Do, Check, Act (PDCA) is a new model of care that identifies the root causes of problems. The study aimed to demonstrate the usefulness of RCA-PDCA nursing methods in preventing intraoperative hypotension during cesarean section and to predict the occurrence of intraoperative hypotension through a machine learning model. METHODS: Patients who underwent cesarean section at Traditional Chinese Medicine of Southwest Medical University from January 2023 to December 2023 were retrospectively screened, and the data of their gestational times, age, height, weight, history of allergies, intraoperative vital signs, fetal condition, operative time, fluid out and in, adverse effects, use of vasopressor drugs, anxiety-depression-pain scores, and satisfaction were collected and analyzed. The statistically different features were screened and five machine learning models were used as predictive models to assess the usefulness of the RCA-PDCA model of care. RESULTS: (1) Compared with the general nursing model, the RCA-PDCA nursing model significantly reduces the incidence of intraoperative hypotension and postoperative complications in cesarean delivery, and the patient experience is comfortable and satisfactory. (2) Among the five machine learning models, the RF model has the best predictive performance, and the accuracy of the random forest model in preventing intraoperative hypotension is as high as 90%. CONCLUSION: Through computer machine learning model analysis, we prove the importance of the RCA-PDCA nursing method in the prevention of intraoperative hypotension during cesarean section, especially the Random Forest model which performed well and promoted the application of artificial intelligence computer learning methods in the field of medical analysis.


Sujet(s)
Césarienne , Hypotension artérielle , Apprentissage machine , Humains , Femelle , Grossesse , Hypotension artérielle/prévention et contrôle , Adulte , Études rétrospectives , Complications peropératoires/prévention et contrôle
13.
Br J Anaesth ; 132(6): 1190-1193, 2024 Jun.
Article de Anglais | MEDLINE | ID: mdl-38677945

RÉSUMÉ

Perioperative anaphylaxis is a rare and unpredictable event that continues to cause patient harm. More work is needed to decrease the risk to patients through measures to limit sensitisation, optimise management and investigation, and ensure that patients are not inadvertently re-exposed to allergens. Robust epidemiological data such as that provided by the consecutive GERAP surveys over the past 30 yr have been invaluable in defining the problem, identifying emerging allergens, acting as a catalyst for change, and stimulating research.


Sujet(s)
Anaphylaxie , Humains , Période périopératoire , Soins périopératoires/méthodes , Hypersensibilité médicamenteuse/diagnostic , Complications peropératoires/prévention et contrôle
14.
BMJ Open ; 14(4): e083606, 2024 Apr 29.
Article de Anglais | MEDLINE | ID: mdl-38684243

RÉSUMÉ

BACKGROUND: Post-induction anaesthesia often promotes intraoperative hypotension (IOH) that can worsen postoperative outcomes. This study aims to assess the benefit of norepinephrine versus ephedrine at the induction of anaesthesia to prevent postoperative complications following major abdominal surgery by preventing IOH. METHODS AND ANALYSIS: The EPON STUDY is a prospective single-centre randomised controlled trial with the planned inclusion of 500 patients scheduled for major abdominal surgery at the Amiens University Hospital. The inclusion criteria are patients aged over 50 years weighing more than 50 kg with an American Society of Anesthesiologists physical status score of ≥2 undergoing major abdominal surgery under general anaesthesia. Patients are allocated either to the intervention group (n=250) or the standard group (n=250). In the intervention group, the prevention of post-induction IOH is performed with norepinephrine (dilution to 0.016 mg/mL) using an electric syringe pump at a rate of 0.48 mg/h (30 mL/h) from the start of anaesthesia and then titrated to achieve the haemodynamic target. In the control group, the prevention of post-induction IOH is performed with manual titration of ephedrine, with a maximal dose of 30 mg, followed by perfusion with norepinephrine. In both groups, the haemodynamic target to maintain is a mean arterial pressure (MAP) of 65 mm Hg or 70 mm Hg for patients with a medical history of hypertension. An intention-to-treat analysis will be performed. The primary outcome is the Clavien-Dindo score assessed up to 30 days postoperatively. The secondary endpoints are the length of hospital stay and length of stay in an intensive care unit/postoperative care unit; postoperative renal function; postoperative cardiovascular, respiratory, neurological, haematological and infectious complications at 1 month; and volume of intraoperative vascular filling and mortality at 1 month. ETHICS AND DISSEMINATION: Ethical approval was obtained from the committee of protection of the persons of Ile de France in May 2021 (number 21 05 41). The authors will be involved in disseminating the research findings (through attending conferences and co-authoring papers). The results of the study will be disseminated via peer-reviewed publications and presentations at national and international conferences. TRIAL REGISTRATION NUMBER: NCT05276596.


Sujet(s)
Abdomen , Éphédrine , Hypotension artérielle , Norépinéphrine , Complications postopératoires , Vasoconstricteurs , Humains , Norépinéphrine/usage thérapeutique , Norépinéphrine/administration et posologie , Abdomen/chirurgie , Complications postopératoires/prévention et contrôle , Études prospectives , Vasoconstricteurs/usage thérapeutique , Vasoconstricteurs/administration et posologie , Hypotension artérielle/prévention et contrôle , Éphédrine/usage thérapeutique , Éphédrine/administration et posologie , Essais contrôlés randomisés comme sujet , Adulte d'âge moyen , Anesthésie générale/effets indésirables , Femelle , Mâle , Complications peropératoires/prévention et contrôle
15.
Adv Skin Wound Care ; 37(5): 238-242, 2024 May 01.
Article de Anglais | MEDLINE | ID: mdl-38648236

RÉSUMÉ

GENERAL PURPOSE: To present research investigating the incidence of and risk factors associated with intraoperative pressure injury in patients undergoing neurologic surgery at Xiangya Hospital, Central South University in China. TARGET AUDIENCE: This continuing education activity is intended for physicians, physician assistants, nurse practitioners, and registered nurses with an interest in skin and wound care. LEARNING OBJECTIVES/OUTCOMES: After participating in this educational activity, the participant will:1. Identify the incidence of intraoperative pressure injuries (PIs) in patients undergoing neurologic surgery at Xiangya Hospital, Central South University in China.2. Describe risk factors for intraoperative PI.3. Outline strategies to help mitigate intraoperative PI risk.


Intraoperative pressure injury (PI) development is an adverse event that impacts thousands of patients globally and is associated with extended hospital stays and increased risk of mortality. To investigate the incidence of intraoperative PI in patients undergoing neurologic surgery and identify associated risk factors. A total of 1,728 patients who underwent neurosurgery in Xiangya Hospital, Central South University between January 2021 and December 2022 were included in this retrospective study. The authors collected patients' demographic data and clinical characteristics and used univariate and multivariate regression to evaluate significant PI risk factors. Intraoperative PI was observed in 1.8% of all surgical cases (n = 31). Having a body mass index greater than 24 kg/m2 (odds ratio, 3.87; 95% CI, 1.62­9.23; P = .002), being in a lateral position (odds ratio, 2.53; 95% CI, 1.04­6.17; P = .042) or a prone position (odds ratio, 10.43; 95% CI, 3.37­32.23; P < .001), and having a longer operation time (cutoff point at 7.92 hours for increased risk of PI; odds ratio, 1.36; 95% CI, 1.21­1.53; P < .001) were significant risk factors for intraoperative PI. This study identified three independent risk factors for intraoperative PI development: body position, surgery duration, and high body mass index. These findings can help OR nurses identify patients who are vulnerable to intraoperative PI and provide appropriate preventive measures. For these patients, perioperative protection and frequent microrepositioning during surgery would be indispensable.


Sujet(s)
Escarre , Humains , Escarre/prévention et contrôle , Escarre/épidémiologie , Escarre/étiologie , Facteurs de risque , Adulte , Chine/épidémiologie , Mâle , Femelle , Incidence , Complications peropératoires/épidémiologie , Complications peropératoires/prévention et contrôle , Complications peropératoires/étiologie , Adulte d'âge moyen , Procédures de neurochirurgie/effets indésirables , Procédures de neurochirurgie/méthodes
17.
Pacing Clin Electrophysiol ; 47(5): 614-625, 2024 May.
Article de Anglais | MEDLINE | ID: mdl-38558218

RÉSUMÉ

INTRODUCTION: The use of esophageal temperature monitoring (ETM) for the prevention of esophageal injury during atrial fibrillation (AF) ablation is often advocated. However, evidence supporting its use is scarce and controversial. We therefore aimed to review the evidence assessing the efficacy of ETM for the prevention of esophageal injury. METHODS: We performed a meta-analysis and systematic review of the available literature from inception to December 31, 2022. All studies comparing the use of ETM, versus no ETM, during radiofrequency (RF) AF ablation and which reported the incidence of endoscopically detected esophageal lesions (EDELs) were included. RESULTS: Eleven studies with a total of 1112 patients undergoing RF AF ablation were identified. Of those patients, 627 were assigned to ETM (56%). The overall incidence of EDELs was 9.8%. The use of ETM during AF ablation was associated with a non significant increase in the incidence of EDELs (12.3% with ETM, vs. 6.6 % without ETM, odds ratio, 1.44, 95%CI, 0.49, 4.22, p = .51, I2 = 72%). The use of ETM was associated with a significant increase in the energy delivered specifically on the posterior wall compared to patients without ETM (mean power difference: 5.13 Watts, 95% CI, 1.52, 8.74, p = .005). CONCLUSIONS: The use of ETM does not reduce the incidence of EDELs during RF AF ablation. The higher energy delivered on the posterior wall is likely attributable to a false sense of safety that may explain the lack of benefit of ETM. Further randomized controlled trials are needed to provide conclusive results.


Sujet(s)
Fibrillation auriculaire , Ablation par cathéter , Oesophage , Humains , Fibrillation auriculaire/chirurgie , Fibrillation auriculaire/prévention et contrôle , Oesophage/traumatismes , Température du corps , Surveillance peropératoire/méthodes , Complications peropératoires/prévention et contrôle
18.
Rev Esp Anestesiol Reanim (Engl Ed) ; 71(3): 151-159, 2024 Mar.
Article de Anglais | MEDLINE | ID: mdl-38452926

RÉSUMÉ

INTRODUCTION: Pulmonary atelectasis is common in patients undergoing laparoscopic abdominal surgery under general anaesthesia, which increases the risk of perioperative respiratory complications. Alveolar recruitment manoeuvres (ARM) are used to open up the lung parenchyma with atelectasis, although the duration of their benefit has not been clearly established. The aim of this study was to determine the effectiveness of an ARM in laparoscopic colon surgery, the duration of response over time, and its haemodynamic impact. METHODS: Twenty-five patients undergoing laparoscopic colon surgery were included. After anaesthetic induction and initiation of surgery with pneumoperitoneum, an ARM was performed, and then optimal PEEP determined. Respiratory mechanics and gas exchange variables, and haemodynamic parameters, were analysed before the manoeuvre and periodically over the following 90 min. RESULTS: Three patients were excluded for surgical reasons. The alveolar arterial oxygen gradient went from 94.3 (62.3-117.8) mmHg before to 60.7 (29.6-91.0) mmHg after the manoeuvre (P < .05). This difference was maintained during the 90 min of the study. Dynamic compliance of the respiratory system went from 31.3 ml/cmH2O (26.1-39.2) before the manoeuvre to 46.1 ml/cmH2O (37.5-53.5) after the manoeuvre (P < .05). This difference was maintained for 60 min. No significant changes were identified in any of the haemodynamic variables studied. CONCLUSION: In patients undergoing laparoscopic colon surgery, performing an intraoperative ARM improves the mechanics of the respiratory system and oxygenation, without associated haemodynamic compromise. The benefit of these manoeuvres lasts for at least one hour.


Sujet(s)
Laparoscopie , Alvéoles pulmonaires , Humains , Laparoscopie/méthodes , Mâle , Femelle , Sujet âgé , Adulte d'âge moyen , Atélectasie pulmonaire/étiologie , Atélectasie pulmonaire/prévention et contrôle , Ventilation à pression positive/méthodes , Côlon/chirurgie , Hémodynamique , Soins peropératoires/méthodes , Complications peropératoires/étiologie , Complications peropératoires/prévention et contrôle , Études prospectives , Pneumopéritoine artificiel/méthodes , Mécanique respiratoire/physiologie
19.
Spine Deform ; 12(4): 961-970, 2024 Jul.
Article de Anglais | MEDLINE | ID: mdl-38556583

RÉSUMÉ

PURPOSE: This study evaluates the intraoperative and short-term complications associated with robotically assisted pedicle screw placement in pediatric posterior spinal fusion (PSF) from three surgeons at two different institutions. METHODS: We retrospectively reviewed 334 pediatric patients who underwent PSF with robotic-assisted navigation at 2 institutions over 3 years (2020-2022). Five thousand seventy robotically placed screws were evaluated. Data collection focused on intraoperative and early postoperative complications with minimum 30-day follow-up. Patients undergoing revision procedures were excluded. RESULTS: Intraoperative complications included 1 durotomy, 6 patients with neuromonitoring alerts not related to screw placement, and 62 screws (1.2%) with documented pedicle breaches, all of which were revised at time of surgery. By quartile, pedicle breaches statistically declined from first quartile to fourth quartile (1.8% vs. 0.56%, p < 0.05). No breach was associated with neuromonitoring changes or neurological sequelae. No spinal cord or vascular injuries occurred. Seventeen postoperative complications occurred in eleven (3.3%) of patients. There were five (1.5%) patients with unplanned return to the operating room. CONCLUSION: Robotically assisted pedicle screw placement was safely and reliably performed on pediatric spinal deformity by three surgeons across two centers, demonstrating an acceptable safety profile and low incidence of unplanned return to the operating room.


Sujet(s)
Vis pédiculaires , Complications postopératoires , Interventions chirurgicales robotisées , Arthrodèse vertébrale , Humains , Arthrodèse vertébrale/méthodes , Arthrodèse vertébrale/effets indésirables , Arthrodèse vertébrale/instrumentation , Vis pédiculaires/effets indésirables , Interventions chirurgicales robotisées/méthodes , Interventions chirurgicales robotisées/effets indésirables , Enfant , Études rétrospectives , Complications postopératoires/épidémiologie , Complications postopératoires/étiologie , Complications postopératoires/prévention et contrôle , Mâle , Femelle , Adolescent , Complications peropératoires/épidémiologie , Complications peropératoires/étiologie , Complications peropératoires/prévention et contrôle
20.
Surg Today ; 54(7): 779-786, 2024 Jul.
Article de Anglais | MEDLINE | ID: mdl-38381178

RÉSUMÉ

PURPOSE: To evaluate the safety and efficacy of new staple-line reinforcement (SLR) in pulmonary resection through a prospective study and to compare the results of this study with historical control data in an exploratory study. METHODS: The subjects of this study were 48 patients who underwent thoracoscopic lobectomy. The primary endpoint was air leakage from the staple line. The secondary endpoints were the location of air leakage, duration of air leakage, and postoperative pulmonary complications. RESULTS: The incidence of intraoperative air leakage from the staple line was 6.3%. Three patients had prolonged air leakage as a postoperative pulmonary complication. No malfunction was found in patients who underwent SLR with the stapling device. When compared with the historical group, the SLR group had a significantly lower incidence of air leakage from the staple line (6.3% vs. 28.5%, P < 0.001) and significantly shorter indwelling chest drainage time (P = 0.049) and length of hospital stay (P < 0.001). CONCLUSIONS: The use of SLR in pulmonary resection was safe and effective. When compared with conventional products, SLR could control intraoperative air leakage from the staple line and shorten time needed for indwelling chest drainage and the length of hospital stay.


Sujet(s)
Durée du séjour , Pneumonectomie , Complications postopératoires , Agrafage chirurgical , Humains , Pneumonectomie/méthodes , Études prospectives , Femelle , Mâle , Agrafage chirurgical/méthodes , Sujet âgé , Adulte d'âge moyen , Complications postopératoires/prévention et contrôle , Complications postopératoires/épidémiologie , Complications postopératoires/étiologie , Résultat thérapeutique , Thoracoscopie/méthodes , Complications peropératoires/prévention et contrôle , Complications peropératoires/épidémiologie , Complications peropératoires/étiologie , Adulte , Incidence , Sécurité , Facteurs temps
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