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Renal manifestations of tuberous sclerosis complex: patients’ and parents’ knowledge and routines for renal follow-up – a questionnaire study

机译:结节性硬化症的肾脏表现:患者和父母的肾脏随访知识和常规–一项问卷调查

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Renal angiomyolipomas (AMLs) are a major clinical feature in patients with tuberous sclerosis complex (TSC). Spontaneous bleeding can be life threatening, and appropriate information and proper surveillance and management are important to limit morbidity and mortality. Because TSC is a rare disease, patients are at risk of suboptimal medical management. Our aim was to investigate patients’ and parents’ knowledge about renal angiomyolipomas (AMLs) in Tuberous Sclerosis Complex (TSC) and to identify current routines for renal follow-up. A questionnaire survey was initiated by the French Reference Centre on TSC. It was distributed in France through university hospitals and the patients’ association (2009-2011), and to patients registered by the Norwegian National Centre for Rare Epilepsy-Related Disorders (2013-2014). Contingency tables with Chi-Square test for independence (with Yates Continuity Correction) and Pearson-Chi-Square value were used for correlation statistics. We included 357 patients (France, n=257; Norway n=100). Most participants knew that TSC is associated with AMLs. However, 42 % did not know about the risk of AMLrelated bleeding, and 37 % had been informed about the risk of bleeding only after the age of 15 years. Furthermore, 14 % did not know whether they themselves or their child had AMLs. Patients had less knowledge than parents. Medical consultations and patient associations were the main sources of information. Among 30 % of patients, renal imaging was not received at all, or not conducted every 1-3 years, as recommended by current guidelines. Regular imaging was more frequent in patients with AMLs < 15 years, than in patients with AMLs ≥ 15 years. Ultrasound was the most frequently used imaging modality. Knowledge of renal AML in TSC patients and their parents was lower than expected, and follow-up by renal imaging was suboptimal for a substantial proportion of patients. Patients and parents should be informed about the risk and symptoms of renal bleeding, at the latest when the patient is 15 years. Monitoring the growth of AMLs should be standardized to comply with guidelines. Transition between adolescence and adulthood is a high-risk period and ensuring appropriate follow-up at this time is particularly important.
机译:肾血管平滑肌脂肪瘤(AML)是结节性硬化症(TSC)患者的主要临床特征。自发性出血可能危及生命,因此适当的信息以及适当的监视和管理对于限制发病率和死亡率很重要。由于TSC是一种罕见的疾病,因此患者处于医疗管理不佳的风险中。我们的目的是调查患者和父母对结节性硬化症(TSC)中肾血管平滑肌脂肪瘤(AML)的了解,并确定当前的肾脏随访程序。法国TSC参考中心发起了问卷调查。该药已在法国通过大学医院和患者协会(2009-2011年)分发给了挪威国家罕见癫痫相关疾病中心(2013-2014年)。相关性使用了具有卡方检验独立性(具有Yates连续性校正)和Pearson-Chi-Square值的列联表。我们纳入了357名患者(法国,n = 257;挪威,n = 100)。大多数参与者都知道TSC与AML相关。但是,有42%的人不知道与AML相关的出血的风险,只有37岁的人中有37%的才知道有出血的风险。此外,有14%的人不知道自己或孩子是否患有AML。患者的知识少于父母。医学咨询和患者协会是主要的信息来源。根据现行指南的建议,在30%的患者中,根本没有或每1-3年未进行肾脏成像检查。 AML≤15岁的患者比≥15岁的AML患者进行常规成像的频率更高。超声是最常用的成像方式。 TSC患者及其父母对肾AML的了解低于预期,并且对于大部分患者而言,通过肾脏成像进行随访的效果欠佳。应当最晚在患者15岁时告知患者和父母有关肾出血的风险和症状。监测AML的增长应标准化以符合准则。青春期和成年期之间的过渡是一个高风险期,因此确保此时适当的随访尤为重要。

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