Long-Term Treatment with Trazodone Once-A-Day (TzOAD) in Patients with MDD: An Observational, Prospective Study

被引:5
作者
Shrashimirova, Milena [1 ]
Tyanev, Ivan [2 ]
Cubala, Wieslaw J. [3 ]
Wichniak, Adam [4 ,5 ]
Vodickova-Borzova, Claudia [6 ]
Ruggieri, Alessandro [7 ,8 ]
Bonelli, Annalisa [7 ]
Lipone, Paola [7 ]
Comandini, Alessandro [7 ]
Cattaneo, Agnese [7 ]
机构
[1] Hosp VITA, Diagnost Consultat Ctr 14, Sofia, Bulgaria
[2] Multiprofile Hosp Act Treatment, Med Clin, Targovishte, Bulgaria
[3] Med Univ Gdansk, Dept Psychiat, Gdansk, Poland
[4] Inst Psychiat & Neurol, Dept Psychiat 3, Warsaw, Poland
[5] Inst Psychiat & Neurol, Sleep Disorders Ctr, Warsaw, Poland
[6] Brain Soultherapy sro, Psychiat & Neurol, Kladno, Czech Republic
[7] Angelini Pharm SpA, Global Med Dept, Rome, Italy
[8] Angelini Pharm SpA, Global Med Dept, Viale Amelia 70, I-00181 Rome, Italy
关键词
major depressive disorder; trazodone; patient-reported outcome; real-world evidence; effectiveness; long-term follow-up; MAJOR DEPRESSIVE DISORDER; SEXUAL DYSFUNCTION; PROLONGED-RELEASE; EFFICACY; VENLAFAXINE; FLUOXETINE; PAROXETINE; SLEEPINESS; SERTRALINE; MECHANISM;
D O I
10.2147/NDT.S399948
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Purpose: This was an observational, prospective, single-group, multicentre, international study aimed to describe the clinical response, functional impairment, and quality of life (QoL) of patients suffering from major depressive disorder (MDD) and in treatment with Trazodone Once-A-Day (TzOAD) monotherapy, over a 24-week period.Patients and Methods: A total of 200 patients with a diagnosis of MDD who had been treated with TzOAD monotherapy were enrolled from 26 sites across 3 European countries (Bulgaria, Czech Republic, and Poland), including psychiatric private practices, and outpatient departments from general and psychiatric hospitals. Study assessments were completed by physicians and patients during routine visits within the normal practice of care.Results: Clinical response was assessed by Clinical Global Impressions - Improvement (CGI-I) responders' percentage at 24 (+/- 4) weeks. The majority of patients (86.5%) reported an improvement on the CGI-I compared to baseline. Results of the study confirm the well-known safety and tolerability of TzOAD, as well as its effectiveness on depressive symptoms, such as improvement in QoL, sleep quality, and overall functioning accompanied by favourable adherence and low drop-out rate. Conclusion: To our knowledge, this is the first observational, long-term study in patients suffering from MDD, conducted with TzOAD. The improvement observed in clinical response, overall functioning, depressive symptoms, and QoL along the 24 weeks (+4) maintenance period and the very good retention rate, suggest that TzOAD may represent an effective and well tolerated treatment option for patients suffering from MDD.
引用
收藏
页码:1181 / 1193
页数:13
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