Your browser doesn't support javascript.
loading
Montrer: 20 | 50 | 100
Résultats 1 - 3 de 3
Filtrer
Plus de filtres











Base de données
Gamme d'année
1.
Eur Arch Otorhinolaryngol ; 281(10): 5473-5480, 2024 Oct.
Article de Anglais | MEDLINE | ID: mdl-38914816

RÉSUMÉ

PURPOSE: To evaluate whether trans-thyroid cartilage nerve monitoring for thyroid surgeries is as effective and safe as endotracheal tube monitoring. METHODS: Fifty-one thyroidectomies (38 hemithyroidectomies and 13 total thyroidectomies, analyzed as two separate hemi-thyroidectomies) were included. Patients undergoing surgery from 6/2020 to 8/2021 were monitored simultaneously with the NIM® Nerve Monitoring System TriVantage™ Electromyography (EMG) endotracheal tube and EMG trans-thyroid cartilage. Electrophysiological responses of 64 vagus and recurrent laryngeal nerves were obtained. Peri-operative evaluation and 12-month post-operative follow-up were conducted to examine nerve function. Wilcoxon signed-rank and Spearman coefficient tests were used to determine whether there were differences between the methods. RESULTS: The average initial amplitude measured with the trans-thyroid cartilage method was higher in the recurrent laryngeal and vagus nerves (p = 0.002, p = 0.003, respectively). The mean difference in EMG amplitude from start to end of surgery for 10 damaged nerves (7 temporary and 3 permanent) differed from intact nerves in both methods and nerves (p < 0.05 for all). Among intact recurrent laryngeal nerves, 20.4% had 20-80% decrease in amplitude in endotracheal tube electrodes and 16.7% in trans-thyroid cartilage electrodes (p = 0.92). All cases with stable EMG signals or with increased EMG amplitude (with both types of electrodes and with both nerves) had normal post-operative vocal function. No significant difference was found between the two methods when measuring the vagus and recurrent laryngeal nerves. No complications occurred when using trans-thyroid cartilage electrodes. CONCLUSIONS: Trans-thyroid cartilage nerve monitoring for thyroid surgeries is as effective and safe as the current standard monitoring using an endotracheal tube. During thyroid surgery, patients are monitored to avoid damaging nerves near the vocal cords. This study compared monitoring through a throat tube with the easier method of monitoring outside of the throat to see if it is as effective and safe. No major difference was found between the two methods and there were no problems.


Sujet(s)
Électromyographie , Intubation trachéale , Surveillance peropératoire , Cartilage thyroïde , Thyroïdectomie , Humains , Thyroïdectomie/méthodes , Thyroïdectomie/effets indésirables , Mâle , Femelle , Intubation trachéale/méthodes , Adulte d'âge moyen , Électromyographie/méthodes , Cartilage thyroïde/chirurgie , Adulte , Surveillance peropératoire/méthodes , Lésions du nerf laryngé récurrent/prévention et contrôle , Lésions du nerf laryngé récurrent/étiologie , Sujet âgé , Nerf laryngé récurrent/physiologie , Nerf vague
2.
Laryngoscope ; 133(5): 1271-1275, 2023 05.
Article de Anglais | MEDLINE | ID: mdl-36354236

RÉSUMÉ

OBJECTIVE: Chronic sialadenitis is the most common complication of radioactive iodine (RAI) treatment. The aim of the study was to ascertain sonographic features of the major salivary glands in patients with papillary thyroid cancer (PTC) treated with RAI. METHODS: The database of a tertiary medical center was retrospectively searched for consecutive patients who underwent total thyroidectomy for PTC in 2011-2020 with ultrasound follow-up after 1 year. Changes in ultrasound features of the major salivary glands were compared between patients treated or not treated with RAI postoperatively. RESULTS: The cohort included 158 patients, of whom 109 (69%) were treated postoperatively with RAI (mean dose, 131 mCi) and 49 were not (control group). Sonographic changes were observed in the major salivary glands in 43% of the study group and 18% of the control group (p = 0.002), including coarse echotexture, decreased echogenicity, fibrosis, and atrophy. Higher RAI doses were significantly correlated with the prevalence and severity of glandular changes (p < 0.0001). CONCLUSION: RAI treatment following thyroidectomy is associated with a dose-response effect and adverse changes in the major salivary glands and should be prescribed carefully. LEVEL OF EVIDENCE: 4 Laryngoscope, 133:1271-1275, 2023.


Sujet(s)
Tumeurs de la thyroïde , Humains , Tumeurs de la thyroïde/imagerie diagnostique , Tumeurs de la thyroïde/radiothérapie , Tumeurs de la thyroïde/chirurgie , Radio-isotopes de l'iode/effets indésirables , Études rétrospectives , Glandes salivaires/imagerie diagnostique , Cancer papillaire de la thyroïde/imagerie diagnostique , Cancer papillaire de la thyroïde/radiothérapie , Cancer papillaire de la thyroïde/chirurgie , Thyroïdectomie
3.
J Crit Care ; 68: 144-154, 2022 04.
Article de Anglais | MEDLINE | ID: mdl-34895959

RÉSUMÉ

BACKGROUND: Our survey aimed to evaluate adherence to Surviving Sepsis Campaign (SSC) Guidelines 2016 among intensive care practitioners and to identify issues that remain controversial or lack clarity. METHODS: Members of the European Society of Intensive Care Medicine (ESICM) were surveyed using an anonymous web-based survey written by an international group of experts. The primary outcome measure was the rate of adherence to specific recommendations. Secondary outcomes were to describe areas of controversy and lack of data and to associate specific practices with clinician characteristics. RESULTS: Overall 820 questionnaires were completed. The SCC recommendations 2016 most adhered to were the choice of norepinephrine as first-line vasoactive drug (96.5%), vasopressor prescription based on therapeutic goal rather than dose (83.4%), targeting a specific mean arterial blood pressure during vasopressor use (77.9%), monitoring of blood pressure invasively (62.8%) and adding vasopressin or epinephrine as a second vasoactive agent (83.4%). We identified an internal conflict with regards to parallel versus sequential administration of fluids and vasoactive drugs and regional differences in practice that may be related to drug availabilities. CONCLUSION: The use of vasopressors and fluid use in septic shock is largely compliant with current guidelines but several controversies should be addressed in future guideline iterations.


Sujet(s)
Sepsie , Choc septique , Traitement par apport liquidien , Humains , Réanimation , Sepsie/traitement médicamenteux , Choc septique/traitement médicamenteux , Enquêtes et questionnaires , Vasoconstricteurs/usage thérapeutique
SÉLECTION CITATIONS
DÉTAIL DE RECHERCHE