Kocaeli University Faculty of Medicine, Department of Ophthalmology, Kocaeli, Turkey.
University of Health Sciences Turkey, Derince Training and Research Hospital, Clinic of Ophthalmology, Kocaeli, Turkey.
Turk J Ophthalmol. 2022 Jun 29;52(3):179-185. doi: 10.4274/tjo.galenos.2021.37075.
To analyze the current preferences of ophthalmologists for the treatment of macular edema and age-related macular degeneration (AMD) and to evaluate off-label use of bevacizumab in Turkey.
All members of the Turkish Ophthalmological Association were contacted by e-mail to complete an anonymous, 47-question internet-based survey. The second part of the survey (questions 36-47) was evaluated.
When current legal regulations were considered, ophthalmologists used bevacizumab as the first-line agent in patients with diabetic macular edema (DME), AMD, and retinal vein occlusion (RVO) (58.25%, 55.89%, and 52.29%, respectively). When economic and legal constraints were disregarded, the participants' preference for bevacizumab in the treatment of DME, AMD, and RVO decreased (11.64%, 10.58%, and 10.93%, respectively). Approximately three-quarters (75.75%) of ophthalmologists stated that dispensing multiple syringes from a single bevacizumab bottle could increase the risk of endophthalmitis. Most participants (93.68%) did not feel legally safe from harm caused by off-label bevacizumab use. However, 66.43% of ophthalmologists stated that bevacizumab is as effective as other anti-vascular endothelial growth factor (anti-VEGF) drugs.
Bevacizumab is widely used as a first-line treatment for all indications of anti-VEGF use in the current reimbursement conditions, which preclude the right of ophthalmologists to treat according to their own preferences.
分析眼科医生目前对治疗黄斑水肿和年龄相关性黄斑变性(AMD)的偏好,并评估贝伐单抗在土耳其的超适应证使用情况。
通过电子邮件联系所有土耳其眼科协会成员,完成一份匿名的、包含 47 个问题的网络调查。评估调查的第二部分(问题 36-47)。
在考虑当前法律规定的情况下,眼科医生将贝伐单抗作为糖尿病性黄斑水肿(DME)、AMD 和视网膜静脉阻塞(RVO)患者的一线治疗药物(分别为 58.25%、55.89%和 52.29%)。当不考虑经济和法律限制时,参与者在治疗 DME、AMD 和 RVO 时对贝伐单抗的偏好程度降低(分别为 11.64%、10.58%和 10.93%)。大约四分之三(75.75%)的眼科医生表示,从一个贝伐单抗瓶中分配多个注射器可能会增加眼内炎的风险。大多数参与者(93.68%)认为,由于贝伐单抗的超适应证使用而遭受的伤害,他们在法律上并不安全。然而,66.43%的眼科医生表示,贝伐单抗与其他抗血管内皮生长因子(anti-VEGF)药物一样有效。
在当前的报销条件下,贝伐单抗被广泛用作所有抗 VEGF 适应证的一线治疗药物,这限制了眼科医生根据自己的偏好进行治疗的权利。