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CATALOGO DEI PRODOTTI DELLA RICERCA
Patients with diabetes mellitus and comorbid cardiovascular disease, chronic kidney disease or cardiorenal disease should be treated with sodium-glucose cotrasporter 2 (SGLT-2) inhibitors, alone or in combination with renin-angiotensin system (RAS) inhibitors, in order to reduce their cardiovascular and renal risk. We conducted a multicenter, retrospective, observational cohort study using data from the Italian REPOSI registry, including 1372 patients with diabetes aged >= 65 years hospitalized with cardiovascular diseases (heart failure or ischemic heart disease), chronic kidney disease or cardiorenal disease, between 2008 and 2024, with the purpose of analyzing the prescription in these patients of SGLT-2 inhibitors, alone or in combination with RAS-inhibitors, before and after the implementation of Note AIFA 100 in 2022. The prescription of SGLT-2 inhibitors alone and also their combination with RAS-inhibitors is scarce in patients with diabetes and cardiovascular, renal and cardiorenal comorbidities attending internal medicine and geriatric Italian wards, across all eGFR categories, with never users ranging from 96.9% to 98.9%. The regulatory implementation of "Nota AIFA 100" only modestly improved the prescription of SGLT-2 inhibitors in these elderly patients, the improvement being about 14% among never users. The scarce utilization of SGLT-2 inhibitors and their combination with RAS inhibitors is still of clinical concern, owing to the maximization of cardiorenal protection that stems from these drugs in patients with diabetes. The reclassification of SGLT-2 inhibitors in the group of products that can be reimbursed in pharmacies, adopted by AIFA in 2025, is expected to produce greater adherence to these important medications.
Prescription of SGLT-2 inhibitors alone or in combination with RAS-inhibitors in patients with diabetes mellitus and comorbid cardiovascular disease, chronic kidney disease or cardiorenal disease: a real-world evidence study from the REPOSI registry
Patients with diabetes mellitus and comorbid cardiovascular disease, chronic kidney disease or cardiorenal disease should be treated with sodium-glucose cotrasporter 2 (SGLT-2) inhibitors, alone or in combination with renin-angiotensin system (RAS) inhibitors, in order to reduce their cardiovascular and renal risk. We conducted a multicenter, retrospective, observational cohort study using data from the Italian REPOSI registry, including 1372 patients with diabetes aged >= 65 years hospitalized with cardiovascular diseases (heart failure or ischemic heart disease), chronic kidney disease or cardiorenal disease, between 2008 and 2024, with the purpose of analyzing the prescription in these patients of SGLT-2 inhibitors, alone or in combination with RAS-inhibitors, before and after the implementation of Note AIFA 100 in 2022. The prescription of SGLT-2 inhibitors alone and also their combination with RAS-inhibitors is scarce in patients with diabetes and cardiovascular, renal and cardiorenal comorbidities attending internal medicine and geriatric Italian wards, across all eGFR categories, with never users ranging from 96.9% to 98.9%. The regulatory implementation of "Nota AIFA 100" only modestly improved the prescription of SGLT-2 inhibitors in these elderly patients, the improvement being about 14% among never users. The scarce utilization of SGLT-2 inhibitors and their combination with RAS inhibitors is still of clinical concern, owing to the maximization of cardiorenal protection that stems from these drugs in patients with diabetes. The reclassification of SGLT-2 inhibitors in the group of products that can be reimbursed in pharmacies, adopted by AIFA in 2025, is expected to produce greater adherence to these important medications.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11562/1204267
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simulazione ASN
Il report seguente simula gli indicatori relativi alla propria produzione scientifica in relazione alle soglie ASN 2023-2025 del proprio SC/SSD. Si ricorda che il superamento dei valori soglia (almeno 2 su 3) è requisito necessario ma non sufficiente al conseguimento dell'abilitazione. La simulazione si basa sui dati IRIS e sugli indicatori bibliometrici alla data indicata e non tiene conto di eventuali periodi di congedo obbligatorio, che in sede di domanda ASN danno diritto a incrementi percentuali dei valori. La simulazione può differire dall'esito di un’eventuale domanda ASN sia per errori di catalogazione e/o dati mancanti in IRIS, sia per la variabilità dei dati bibliometrici nel tempo. Si consideri che Anvur calcola i valori degli indicatori all'ultima data utile per la presentazione delle domande.
La presente simulazione è stata realizzata sulla base delle specifiche raccolte sul tavolo ER del Focus Group IRIS coordinato dall’Università di Modena e Reggio Emilia e delle regole riportate nel DM 589/2018 e allegata Tabella A. Cineca, l’Università di Modena e Reggio Emilia e il Focus Group IRIS non si assumono alcuna responsabilità in merito all’uso che il diretto interessato o terzi faranno della simulazione. Si specifica inoltre che la simulazione contiene calcoli effettuati con dati e algoritmi di pubblico dominio e deve quindi essere considerata come un mero ausilio al calcolo svolgibile manualmente o con strumenti equivalenti.