Physicians' and Patients' Perceptions and Practices Concerning Antithyroid Drug-Induced Agranulocytosis

S. Beshyah, A. E. Bashier, B. Afandi, Mohammed Naman Mohammed, E. Abdelgadir, A. Beshyah
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Abstract

Abstract Objectives  We aimed to ascertain physicians' attitudes and practices and evaluate patients' knowledge of antithyroid drugs (ATDs). Also, we would like to review the quality of patients' information on the Internet (in Arabic) concerning ATDs' including agranulocytosis. Methods  A mixed methods study design was employed, including an online physician questionnaire, structured interviews of patients on ATDs, and evaluation on web sites containing patients' information in Arabic. Results  Most physicians (82.6%) thought the frequency of agranulocytosis in patients receiving antithyroid medications is 1 to 5 per 1,000 per annum. Nearly 72% of the participants reported educating their patients about the risk of agranulocytosis when they receive ATDs regularly verbally only. Most physicians thought patients should be warned about sore throat and fever. More participants would measure a white blood cell (WBC) count only if a patient developed suggestive symptoms (57.0%) than those who do it routinely (43.0%). If a patient receiving ATDs develops suspicious symptoms, participants thought that the most efficient way to deal with this is to attend the nearest hospital emergency department (37.2%). Less thought they can go to any facility with a laboratory that can do WBC count (29.8%) or contact their usual endocrine clinic (24.4%). Nearly half of the patients (49%) were aware of the side effects of ATDs, but only 17 respondents (17.3%) identified one or both of the two most typical symptoms of agranulocytosis. The quality of the information received was evaluated as “not good at all” or “poor” by 19.2%. Over two-thirds (69.7%) of participants thought the amount of information was about right. Most participants (72.5%) preferred receiving information on side effects during consultations with their physicians. Since starting ATDs, 37.0% of patients have experienced different symptoms suggestive of agranulocytosis in various combinations. However, only one-third (12/37) had an urgent blood count. A review of 190 selected Arabic patient information Internet sites revealed a significant variation in patient advice. Six percent 11/190 (5.8%) of the sites can be considered good. Conclusions  The findings of suboptimal and inconsistent perceptions and practices of physicians and patients put patients with ATD in the Middle East at increased risk and call for more action from professional and patient advocacy groups.
医生和患者对抗甲状腺药物性粒细胞缺乏症的认知和实践
摘要目的了解医生对抗甲状腺药物的态度和做法,并评价患者对抗甲状腺药物(ATDs)的认知。此外,我们希望回顾互联网(阿拉伯语)上关于ATDs(包括粒细胞缺乏症)的患者信息的质量。方法采用混合方法的研究设计,包括在线医生问卷,对ATDs患者进行结构化访谈,以及对包含阿拉伯语患者信息的网站进行评估。结果大多数医生(82.6%)认为接受抗甲状腺药物治疗的患者出现粒细胞缺乏症的频率为1 ~ 5 / 1000。近72%的参与者报告说,当他们定期口头接受ATDs时,他们会教育患者有关粒细胞缺乏症的风险。大多数医生认为应该提醒病人注意喉咙痛和发烧。只有在患者出现暗示症状时才测量白细胞(WBC)计数的参与者(57.0%)比常规检测的参与者(43.0%)要多。如果接受ATDs治疗的患者出现可疑症状,参与者认为最有效的处理方法是到最近的医院急诊科就诊(37.2%)。较少的人认为他们可以去任何有白细胞计数实验室的机构(29.8%)或联系他们通常的内分泌诊所(24.4%)。近一半的患者(49%)意识到ATDs的副作用,但只有17名受访者(17.3%)确定了粒细胞缺乏症的两种最典型症状中的一种或两种。收到的信息质量评价为“完全不好”或“差”的占19.2%。超过三分之二(69.7%)的参与者认为信息量大致正确。大多数参与者(72.5%)更愿意在咨询医生时获得有关副作用的信息。自ATDs开始以来,37.0%的患者经历了不同组合的提示粒细胞缺乏症的不同症状。然而,只有三分之一(12/37)有紧急血液计数。对190个选定的阿拉伯患者信息互联网站点的回顾揭示了患者建议的显著差异。6 /190(5.8%)的网站可以被认为是好的。医生和患者的不理想和不一致的认知和实践的发现使中东的ATD患者面临更高的风险,并呼吁专业和患者倡导团体采取更多行动。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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