Gli oncologi, l’intervento tempestivo aiuta la cura. La chemioterapia probabilmente è preventiva per evitare le recidive
Risultati per: Scoperto bersaglio per il trattamento del cancro al pancreas
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Istituita la cabina di regia per la Rete Centri Pancreas Unit
Al ministero della Salute, coordinata da Sergio Alfieri
Salute, istituita cabina di regia per la Rete Centri Pancreas Unit
Comunicato del 20/03/2024 n°16
Diagnosi e trattamento della rinite allergica
Algoritmo di trattamento per la terapia medica guidata dalle linee guida nello scompenso cardiaco a frazione d’eiezione ridotta
Linee guida sulla diagnosi e gestione del cancro al polmone
Trattamento dell’insufficienza cardiaca con frazione di eiezione ridotta
Sildenafil come potenziale trattamento per il morbo di Alzheimer
Study protocol for a randomised open-label clinical trial examining the safety and efficacy of the Android Artificial Pancreas System (AAPS) with advanced bolus-free features in adults with type 1 diabetes: the 'CLOSE IT (Closed Loop Open SourcE In Type 1 diabetes) trial
Introduction
Multiple automated insulin delivery (AID) systems have become commercially available following randomised controlled trials demonstrating benefits in people with type 1 diabetes (T1D). However, their real-world utility may be undermined by user-associated burdens, including the need to carbohydrate count and deliver manual insulin boluses. There is an important need for a ‘fully automated closed loop’ (FCL) AID system, without manual mealtime boluses. The (Closed Loop Open SourcE In Type 1 diabetes) trial is a randomised trial comparing an FCL AID system to the same system used as a hybrid closed loop (HCL) in people with T1D, in an outpatient setting over an extended time frame.
Methods and analysis
Randomised, open-label, parallel, non-inferiority trial comparing the Android Artificial Pancreas System (AAPS) AID algorithm used as FCL to the same algorithm used as HCL. Seventy-five participants aged 18–70 will be randomised (1:1) to one of two treatment arms for 12 weeks: (a) FCL—participants will be advised not to bolus for meals and (b) HCL—participants will use the AAPS AID algorithm as HCL with announced meals. The primary outcome is the percentage of time in target sensor glucose range (3.9–10.0 mmol/L). Secondary outcomes include other glycaemic metrics, safety, psychosocial factors, platform performance and user dietary factors. Twenty FCL arm participants will participate in a 4-week extension phase comparing glycaemic and dietary outcomes using NovoRapid (insulin aspart) to Fiasp (insulin aspart and niacinamide).
Ethics and dissemination
Approvals are by the Alfred Health Ethics Committee (615/22) (Australia) and Health and Disability Ethics Committees (2022 FULL 13832) (New Zealand). Each participant will provide written informed consent. Data protection and confidentiality will be ensured. Study results will be disseminated by publications, conferences and patient advocacy groups.
Trial registration numbers
ACTRN12622001400752 and ACTRN12622001401741.
Studio Usa: a Chernobyl lupi mutanti resistenti al cancro
Gli animali si espongono alle radiazioni cancerogene mentre vagano per la città ucraina, abbandonata dopo un incidente nucleare nel 1986. Secondo i ricercatori di Priceton parte delle loro informazioni genetiche sembrano resistenti all’aumento del rischio di malattia
Verso un test delle urine per la diagnosi precoce del cancro alle ovaie
Miglioramento della sopravvivenza a 5 anni se il tumore è in fase precoce
Linee guida sul trattamento chirurgico della fibrillazione atriale
Tumore del pancreas, scoperto come la malattia sfugge alle cure
Usa un trucco genetico. Studio apre a nuove cure
Non solo cancro, più rischi cardiovascolari in donne con Hpv
Il rischio di morte è 4 volte più alto, vaccino potrebbe ridurlo
Giornata mondiale cancro, Schillaci: “Prevenire è fondamentale, forte impegno per adesione a screening e stili di vita corretti”
Comunicato del 04/02/2024 n°7
A Novel Approach for Pancreas Transcriptomics Reveals the Cellular Landscape in Homeostasis and Acute Pancreatitis
Acinar cells produce digestive enzymes that impede transcriptomic characterization of the exocrine pancreas. Thus, single-cell RNA-sequencing (scRNA-seq) studies of the pancreas underrepresent acinar cells relative to histological expectations, and a robust approach to capture pancreatic cell responses in disease states is needed. We sought to innovate a method that overcomes these challenges to accelerate study of the pancreas in health and disease.