Titre : Essais d'équivalence comme sujet

Essais d'équivalence comme sujet : Questions médicales fréquentes

Termes MeSH sélectionnés :

Robotics
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[ { "@type": "MedicalWebPage", "name": "Diagnostic", "headline": "Diagnostic sur Essais d'équivalence comme sujet", "description": "Comment évaluer l'équivalence d'un traitement ?\nQuels critères sont utilisés pour l'équivalence ?\nQuelles méthodes statistiques sont appliquées ?\nComment choisir un groupe témoin ?\nQuel est le rôle des biais dans ces essais ?", "url": "https://questionsmedicales.fr/mesh/D000074099?mesh_terms=Robotics&page=1000#section-diagnostic" }, { "@type": "MedicalWebPage", "name": "Symptômes", "headline": "Symptômes sur Essais d'équivalence comme sujet", "description": "Quels symptômes sont mesurés dans les essais d'équivalence ?\nComment les symptômes influencent-ils les résultats ?\nLes effets secondaires sont-ils pris en compte ?\nComment les symptômes sont-ils rapportés ?\nY a-t-il des symptômes spécifiques à surveiller ?", "url": "https://questionsmedicales.fr/mesh/D000074099?mesh_terms=Robotics&page=1000#section-symptômes" }, { "@type": "MedicalWebPage", "name": "Prévention", "headline": "Prévention sur Essais d'équivalence comme sujet", "description": "Les essais d'équivalence incluent-ils des mesures préventives ?\nComment évaluer l'impact préventif d'un traitement ?\nQuelles populations sont ciblées pour la prévention ?\nLes recommandations de prévention sont-elles basées sur ces essais ?\nComment les résultats influencent-ils les pratiques préventives ?", "url": "https://questionsmedicales.fr/mesh/D000074099?mesh_terms=Robotics&page=1000#section-prévention" }, { "@type": "MedicalWebPage", "name": "Traitements", "headline": "Traitements sur Essais d'équivalence comme sujet", "description": "Quels types de traitements sont comparés ?\nComment déterminer l'équivalence des traitements ?\nLes traitements alternatifs sont-ils inclus ?\nQuel est l'impact des traitements sur la qualité de vie ?\nComment les traitements sont-ils administrés ?", "url": "https://questionsmedicales.fr/mesh/D000074099?mesh_terms=Robotics&page=1000#section-traitements" }, { "@type": "MedicalWebPage", "name": "Complications", "headline": "Complications sur Essais d'équivalence comme sujet", "description": "Quelles complications sont surveillées dans les essais ?\nComment les complications affectent-elles l'équivalence ?\nLes complications sont-elles rapportées par les patients ?\nComment minimiser les complications dans les essais ?\nLes complications influencent-elles la durée de l'essai ?", "url": "https://questionsmedicales.fr/mesh/D000074099?mesh_terms=Robotics&page=1000#section-complications" }, { "@type": "MedicalWebPage", "name": "Facteurs de risque", "headline": "Facteurs de risque sur Essais d'équivalence comme sujet", "description": "Quels facteurs de risque sont pris en compte ?\nComment les facteurs de risque influencent-ils les résultats ?\nLes facteurs de risque sont-ils évalués au début de l'essai ?\nComment les facteurs de risque sont-ils mesurés ?\nLes facteurs de risque peuvent-ils changer durant l'essai ?", "url": "https://questionsmedicales.fr/mesh/D000074099?mesh_terms=Robotics&page=1000#section-facteurs de risque" } ] }, { "@type": "FAQPage", "mainEntity": [ { "@type": "Question", "name": "Comment évaluer l'équivalence d'un traitement ?", "position": 1, "acceptedAnswer": { "@type": "Answer", "text": "L'équivalence est évaluée par des essais cliniques comparant les résultats des traitements." } }, { "@type": "Question", "name": "Quels critères sont utilisés pour l'équivalence ?", "position": 2, "acceptedAnswer": { "@type": "Answer", "text": "Les critères incluent des mesures de résultats cliniques, de sécurité et de tolérance." } }, { "@type": "Question", "name": "Quelles méthodes statistiques sont appliquées ?", "position": 3, "acceptedAnswer": { "@type": "Answer", "text": "Des méthodes comme l'intervalle de confiance et les tests de différence sont couramment utilisées." } }, { "@type": "Question", "name": "Comment choisir un groupe témoin ?", "position": 4, "acceptedAnswer": { "@type": "Answer", "text": "Le groupe témoin doit être comparable en termes de caractéristiques démographiques et cliniques." } }, { "@type": "Question", "name": "Quel est le rôle des biais dans ces essais ?", "position": 5, "acceptedAnswer": { "@type": "Answer", "text": "Les biais peuvent fausser les résultats, d'où l'importance de la randomisation et du double aveugle." } }, { "@type": "Question", "name": "Quels symptômes sont mesurés dans les essais d'équivalence ?", "position": 6, "acceptedAnswer": { "@type": "Answer", "text": "Les symptômes varient selon les traitements, mais incluent souvent douleur, fatigue et qualité de vie." } }, { "@type": "Question", "name": "Comment les symptômes influencent-ils les résultats ?", "position": 7, "acceptedAnswer": { "@type": "Answer", "text": "Les symptômes peuvent affecter l'adhérence au traitement et la perception de son efficacité." } }, { "@type": "Question", "name": "Les effets secondaires sont-ils pris en compte ?", "position": 8, "acceptedAnswer": { "@type": "Answer", "text": "Oui, les effets secondaires sont cruciaux pour évaluer l'équivalence et la sécurité des traitements." } }, { "@type": "Question", "name": "Comment les symptômes sont-ils rapportés ?", "position": 9, "acceptedAnswer": { "@type": "Answer", "text": "Les symptômes sont souvent rapportés par les patients via des questionnaires standardisés." } }, { "@type": "Question", "name": "Y a-t-il des symptômes spécifiques à surveiller ?", "position": 10, "acceptedAnswer": { "@type": "Answer", "text": "Oui, des symptômes spécifiques peuvent être surveillés selon la pathologie traitée et le traitement." } }, { "@type": "Question", "name": "Les essais d'équivalence incluent-ils des mesures préventives ?", "position": 11, "acceptedAnswer": { "@type": "Answer", "text": "Oui, certains essais évaluent l'efficacité des interventions préventives par rapport à des traitements standards." } }, { "@type": "Question", "name": "Comment évaluer l'impact préventif d'un traitement ?", "position": 12, "acceptedAnswer": { "@type": "Answer", "text": "L'impact préventif est évalué par la réduction des événements indésirables dans les groupes traités." } }, { "@type": "Question", "name": "Quelles populations sont ciblées pour la prévention ?", "position": 13, "acceptedAnswer": { "@type": "Answer", "text": "Les populations à risque sont souvent ciblées pour maximiser l'impact des interventions préventives." } }, { "@type": "Question", "name": "Les recommandations de prévention sont-elles basées sur ces essais ?", "position": 14, "acceptedAnswer": { "@type": "Answer", "text": "Oui, les recommandations de prévention s'appuient souvent sur les résultats d'essais d'équivalence." } }, { "@type": "Question", "name": "Comment les résultats influencent-ils les pratiques préventives ?", "position": 15, "acceptedAnswer": { "@type": "Answer", "text": "Les résultats des essais d'équivalence peuvent modifier les pratiques cliniques et les protocoles de prévention." } }, { "@type": "Question", "name": "Quels types de traitements sont comparés ?", "position": 16, "acceptedAnswer": { "@type": "Answer", "text": "Les traitements peuvent inclure des médicaments, des thérapies physiques ou des interventions chirurgicales." } }, { "@type": "Question", "name": "Comment déterminer l'équivalence des traitements ?", "position": 17, "acceptedAnswer": { "@type": "Answer", "text": "L'équivalence est déterminée par des résultats cliniques similaires dans des populations comparables." } }, { "@type": "Question", "name": "Les traitements alternatifs sont-ils inclus ?", "position": 18, "acceptedAnswer": { "@type": "Answer", "text": "Oui, les traitements alternatifs peuvent être inclus pour évaluer leur efficacité par rapport aux standards." } }, { "@type": "Question", "name": "Quel est l'impact des traitements sur la qualité de vie ?", "position": 19, "acceptedAnswer": { "@type": "Answer", "text": "Les traitements doivent améliorer la qualité de vie, un critère essentiel dans les essais d'équivalence." } }, { "@type": "Question", "name": "Comment les traitements sont-ils administrés ?", "position": 20, "acceptedAnswer": { "@type": "Answer", "text": "Les traitements peuvent être administrés par voie orale, intraveineuse ou topique, selon le cas." } }, { "@type": "Question", "name": "Quelles complications sont surveillées dans les essais ?", "position": 21, "acceptedAnswer": { "@type": "Answer", "text": "Les complications peuvent inclure des effets indésirables graves ou des échecs de traitement." } }, { "@type": "Question", "name": "Comment les complications affectent-elles l'équivalence ?", "position": 22, "acceptedAnswer": { "@type": "Answer", "text": "Les complications peuvent influencer l'évaluation de l'équivalence en affectant les résultats cliniques." } }, { "@type": "Question", "name": "Les complications sont-elles rapportées par les patients ?", "position": 23, "acceptedAnswer": { "@type": "Answer", "text": "Oui, les patients rapportent souvent les complications via des questionnaires ou des journaux de bord." } }, { "@type": "Question", "name": "Comment minimiser les complications dans les essais ?", "position": 24, "acceptedAnswer": { "@type": "Answer", "text": "Des protocoles rigoureux et une surveillance étroite aident à minimiser les complications durant les essais." } }, { "@type": "Question", "name": "Les complications influencent-elles la durée de l'essai ?", "position": 25, "acceptedAnswer": { "@type": "Answer", "text": "Oui, des complications imprévues peuvent prolonger la durée de l'essai et affecter les résultats." } }, { "@type": "Question", "name": "Quels facteurs de risque sont pris en compte ?", "position": 26, "acceptedAnswer": { "@type": "Answer", "text": "Les facteurs de risque incluent l'âge, le sexe, les comorbidités et les antécédents médicaux." } }, { "@type": "Question", "name": "Comment les facteurs de risque influencent-ils les résultats ?", "position": 27, "acceptedAnswer": { "@type": "Answer", "text": "Les facteurs de risque peuvent modifier l'efficacité des traitements et la survenue de complications." } }, { "@type": "Question", "name": "Les facteurs de risque sont-ils évalués au début de l'essai ?", "position": 28, "acceptedAnswer": { "@type": "Answer", "text": "Oui, une évaluation initiale des facteurs de risque est essentielle pour la stratification des participants." } }, { "@type": "Question", "name": "Comment les facteurs de risque sont-ils mesurés ?", "position": 29, "acceptedAnswer": { "@type": "Answer", "text": "Les facteurs de risque sont mesurés par des questionnaires, des examens cliniques et des tests de laboratoire." } }, { "@type": "Question", "name": "Les facteurs de risque peuvent-ils changer durant l'essai ?", "position": 30, "acceptedAnswer": { "@type": "Answer", "text": "Oui, les facteurs de risque peuvent évoluer, nécessitant une surveillance continue et des ajustements." } } ] } ] }

Sources (10000 au total)

Active smoking increases risk of wound complications in robotic enhanced-view totally extraperitoneal (eTEP) retro-rectus ventral hernia repairs.

Tobacco smoking increases risk of complications after open hernia repair, however it is unknown whether this is true in minimally invasive hernia repair. We aim to determine whether there are differen... Our study included 102 patients who underwent robotic eTEP retrorectus repair of ventral hernias at a single institution from November 2019 to October 2022. Data collected included demographics, smoki... Out of 102 patients, 18 were currently smoking, 38 were former smokers, 56 had ever smoked, 46 had never smoked and 84 were not currently smoking. Those who had ever smoked were more likely to endorse... Active smoking at the time of robotic eTEP increases the risk of clinically significant surgical site occurrences. This same increase is not seen in former smokers suggesting that smoking cessation sh...

The Conversion of Unicompartmental Knee Arthroplasty to Total Knee Arthroplasty with Non-CT Based Robotic Assistance: A Novel Surgical Technique and Case Series.

Robotic-assisted devices help provide precise component positioning in conversion of unicompartmental knee arthroplasty (UKA) to total knee arthroplasty (TKA). A few studies offer surgical techniques ... We present three patients (ages 46 to 66) who were evaluated for conversion of UKA to TKA for aseptic loosening, stress fracture, and progressive osteoarthritis. Each patient underwent robotic-assiste... Preoperative planning included biplanar long leg radiographs to determine the anatomic and mechanical axis of the leg. After arthrotomy with a standard medial parapatellar approach, infrared reflector... The use of a non-CT based robotic assisted device in conversion of UKA to TKA is a novel technique and a good option for surgeons familiar with robotic-assisted arthroplasty, resulting in excellent ou...

Effect and optimal exercise prescription of robot-assisted gait training on lower extremity motor function in stroke patients: a network meta-analysis.

This study aimed to evaluate the effectiveness of robot-assisted gait training (RAGT) and explore the optimal exercise prescription using a network meta-analysis approach.... A comprehensive search was conducted on randomized controlled trials comparing robotic and conventional rehabilitation published up to January 2024 in PubMed, Web of Science, Cochrane Library, Embase,... The evaluation parameters included Fugl-Meyer Assessment of Lower Extremity (FMA-LE), Functional Ambulation Category (FAC), Berg Balance Scale (BBS), and 6-Minute Walk Test (6MWT). Two investigators i... A total of 21 articles involving 822 subjects were included in the analysis. RAGT positively influenced FMA-LE score (MD = 3.74, 95%CI 3.02-4.46, P < 0.05), FAC score (MD = 0.31, 95%CI 0.1-0.53, P < 0... RAGT can effectively improve lower limb motor function, walking function, balance function, and walking endurance in stroke patients. For optimal improvement in FMA-LE score, an exercise time of 40-60...

Robotic arm-assisted versus conventional total knee arthroplasty: comparing complications, costs, and postoperative opioid use in propensity-matched cohorts.

Limited literature exists substantiating benefits of robotic arm-assisted total knee arthroplasty (raTKA) over conventional total knee arthroplasty (cTKA). This study compared postoperative pain, comp... A commercially available patient database was used for this study. Patients with raTKA and cTKA were identified with current procedural terminology and international classification of diseases (ICD-9/... Compared with patients with cTKAs (n = 31,105), patients with raTKAs (n = 6,221) had less postoperative opioid use (p < 0.01), lower rates of postoperative acute renal failure (OR 0.71; p < 0.01), ane... RaTKA was associated with less postoperative pain and complications compared with cTKA....

Features related to temporary tracheotomy in patients undergoing Transoral Robotic Surgery (TORS) for supraglottic squamous cell cancer of the larynx: A systematic review.

The aim of this systematic review is to assess a relation between demographical, clinical and tumoral features and the need for a prophylactic tracheotomy during TORS procedure in patients affected by... PRISMA 2020 guidelines were applied in this systematic literature review. A computerized search was performed using the Embase/Pubmed, Scopus and Cochrane database, for articles published from 2007 to... Through a study selection process 8 full texts were eligible for statistical univariate analysis. The most relevant factor related to a prophylactic tracheotomy was a contextual bilateral cervical nod... The prophylactic tracheotomy is considered a temporary protection strategy to achieve a valid recovery after TORS procedure. However, there are no guidelines regarding its routinely use. Only 25 % of ...

Win ratio analysis of short-term clinical outcomes of focal therapy and robot-assisted radical prostatectomy for the patients with localized prostate cancer.

We compared the comprehensive clinical outcomes of focal therapy (FT) and robot-assisted radical prostatectomy (RARP) in patients with localized prostate cancer (PC) using a win ratio analysis. After ...

Postoperative Complications and Readmission Rates in Robotic-Assisted Versus Manual Total Knee Arthroplasty: Large, Propensity Score-Matched Patient Cohorts.

There is a paucity of research comparing postoperative complication rates between manual total knee arthroplasty (M-TKA) and robotic-assisted total knee arthroplasty (RA-TKA). This study aims to compa... A retrospective review of a multihospital database identified patients who underwent TKA between January 2016 and May 2023. Surgeons who used the robotic-assisted surgery technique in <10% or >90% of ... All-cause 90-day readmission rates were 2.4% for RA-TKA and 2.6% for M-TKA (P = 0.36). RA-TKA had fewer revisits (RA-TKA: 7.8%; M-TKA: 8.8%, P = 0.027) and rates of readmission with >23 hours of obser... In this retrospective matched cohort analysis, RA-TKA was associated with markedly fewer revisits and readmissions with >23 hours of observation compared with M-TKA. No differences in all-cause 90-day... Level III.... Retrospective review....

Implementation and Validation of a High-Fidelity Simulation Model for Surgical Resident Training: Management of Acute Intraoperative Hemorrhage during Robot-assisted Surgery.

To improve our previous simulation-based training module by using sustainable material to mold an anatomically accurate terrain and reproducing major vascular injuries encountered during robot-assiste... The simulator was built with a pump, gauge, and valve linked via silicone tubing. Artificial blood was made from cornstarch, water, and red dye, and pumped through 3D-Med artificial vessels with the d... The apparatus demonstrated high reproducibility across all simulation scenarios, enhancing resident problem-solving skills. Residents' pre-simulation surveys revealed significant concern regarding the... The management of acute hemorrhage during robot-assisted surgery remains a space for additional surgical education and training. Our simulation successfully provided a reliable, reproducible training ...