Prescription of Sulphonylureas among Patients with Type 2 Diabetes Mellitus in Italy: Results from the Retrospective, Observational Multicentre Cross-Sectional SUSCIPE (Sulphonyl_UreaS_Correct_Internal_Prescription_Evaluation) Study

被引:6
作者
Giorda, Carlo Bruno [1 ]
Orsi, Emanuela [2 ]
De Cosmo, Salvatore [3 ]
Bossi, Antonio Carlo [4 ]
Guerzoni, Catia [5 ]
Cercone, Stefania [5 ]
Gilio, Barbara [5 ]
Cavalot, Franco [6 ]
机构
[1] Azienda Sanitaria Locale TO5, Diabet Unit, Chieri, TO, Italy
[2] Univ Milan, Fdn IRCCS Ca Granda Osped Maggiore Policlin, Dept Med Sci, Endocrinol & Diabet Unit, Milan, Italy
[3] IRCCS Osped Casa Sollievo Sofferenza, Dept Med Sci, San Giovanni Rotondo, FG, Italy
[4] ASST Bergamo Ovest, Osped Treviglio, Diabet Reg Ctr, Endocrine Dis Unit, Treviglio, BG, Italy
[5] MSD Italia Srl, Rome, Italy
[6] San Luigi Gonzaga Hosp, Metab Dis & Diabet Unit, Orbassano, TO, Italy
关键词
Diabetes mellitus; Elderly; Hypoglycemia; Overweight; Obesity; Sulphonylureas; CARDIOVASCULAR OUTCOMES; DISEASE; COMPLICATIONS; RISK;
D O I
10.1007/s13300-020-00871-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction Recent guidelines for the treatment of type 2 diabetes mellitus (T2DM) provide evidence supporting limited use of sulphonylureas (SUs), especially in specific risk patient categories, yet data from national registries still suggest their widespread use. The aim of this study was to investigate characteristics of patients with diabetes treated with SUs and quantify the proportion of patients that met the recommendations for use of SUs by recent guidelines and of those presenting characteristics representing an inappropriate prescription risk (IPR). Methods A multicenter, retrospective, cross-sectional, observational study in patients with T2DM receiving treatment with SUs (as monotherapy or in combination with another diabetes therapy) was conducted between 2017 and 2018 in 22 outpatient diabetes clinics across Italy. Exclusion criteria were type 1 diabetes, diabetes mellitus secondary to other conditions, and presence of severe/life-threatening diseases. Results A total of 510 patients with T2DM (306 men, 204 women; mean age +/- standard deviation 69.8 +/- 9.3 years) who were receiving treatment with a SU (as monotherapy or in combination therapy) were assessed in the study. Overall, 70.6% [n = 360; 95% confidence interval (CI) 66.4%, 74.5%] were assessed to have an IPR. Of these, approximately half presented one factor for risk of inappropriate prescription, and 27 and 10.6% presented two and three factors, respectively. In terms of factors contributing to the total burden of risk of inappropriate treatment with SUs, 37.5% (95% CI 33.2%, 41.8%) of all patients were obese; 33.3% (95% CI 29.3%, 37.6%)] were aged >= 75 years; 18.6% (95% CI 15.3%, 22.3%) had a history of cardiovascular disease; 14.1% (95% CI 11.2%, 17.4%) had chronic renal insufficiency; 1.8% (95% CI 0.8%, 3.3%) had a history of severe hypoglycemia; 1.8% (95% CI 0.8%; 3.3%) had cognitive impairment; and 2.4% (95% CI 1.2%, 4.1%) had a risky occupation. Conclusions The results of this study provide evidence of a high rate of inappropriate SU prescription risk among patients with T2DM, especially among those with overweight/obesity, older age, history of cardiovascular disease, and hypoglycemia.
引用
收藏
页码:2105 / 2119
页数:15
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