首页> 外文期刊>BMC Health Services Research >Increasing access to specialty care for rare diseases: a case study using a foundation sponsored clinic network for patients with neurofibromatosis 1, neurofibromatosis 2, and schwannomatosis
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Increasing access to specialty care for rare diseases: a case study using a foundation sponsored clinic network for patients with neurofibromatosis 1, neurofibromatosis 2, and schwannomatosis

机译:越来越多地获得罕见病的专科护理:使用基金会赞助的临床网络对神经纤维瘤病1,神经纤维瘤病2和神经鞘瘤病患者进行案例研究

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Our primary aim was to assess the ability of a non-profit foundation-sponsored clinic network to facilitate access to specialized care for patients with neurofibromatoses (NF), a group of neurogenetic disorders including NF1, NF2, and schwannomatosis (SWN). Our secondary aim was to identify how our findings in NF could be applied more broadly to other rare diseases. We retrospectively reviewed aggregate data on patient volume reported by specialty NF clinics in a nonprofit network from 2008 to 2015. We classified clinics as high or low volume for disease type (NF1 and NF2/schwannomatosis) and pediatric/adult care. We compared clinic-level data to self-reported patient-level data from a large online patient registry. Between 2008 and 2015, the number of certified NF clinics grew from 32 to 50, and annual patient volume rose from 6776 to 10,245 patients (13% of the total estimated U.S. NF patient population). For patient registry participants (n?=?4476), the median driving distance to the nearest network clinic was 51.3?miles. Driving distances to reach high-volume centers were elevated for adults compared to children (295.8 vs. 67.9?miles), and schwannomatosis and NF2 patients compared to NF1 patients (310.9 vs. 368.1 vs. 161.7?miles). Of registry participants reporting their location of care (n?=?2271), only 43.2% received care in a network specialty clinic, with especially low rates of attendance in the Southwest and Far West. While the number of certified NF clinics and volume of patients seen in these clinics has increased, many NF patients still do not attend specialty clinics and/or travel a significant distance for care. Geographic access to care is more limited for adults, patients with rarer conditions, and patients in the Western U.S. Potential measures to improve access to specialty care for people living with NF and other rare diseases are discussed.
机译:我们的主要目的是评估非盈利性基金会赞助的诊所网络为神经纤维瘤(NF),一组包括NF1,NF2和神经鞘瘤(SWN)在内的神经遗传性疾病的患者提供专业护理的能力。我们的次要目标是确定我们在NF中的发现如何可以更广泛地应用于其他罕见疾病。我们回顾性地回顾了2008年至2015年非营利性网络中专业NF诊所报告的患者数量的汇总数据。我们将诊所分类为疾病类型(NF1和NF2 /神经鞘瘤病)和儿科/成人护理的高或低数量。我们将诊所级别的数据与来自大型在线患者注册表的自我报告的患者级别数据进行了比较。在2008年至2015年之间,经过认证的NF诊所数量从32个增加到50个,年患者数量从6776名增加到10245名患者(占美国NF估计患者总数的13%)。对于患者登记参与者(n = 4476),到最近的网络诊所的平均驾驶距离为51.3英里。与儿童相比,成人到大容量中心的行驶距离有所增加(295.8对67.9英里),神经鞘瘤病和NF2患者与NF1患者相比(310.9对368.1对161.7英里)有所增加。在报告其就诊地点的登记注册参与者中(n = 2271),只有43.2%的人在网络专科诊所接受了护理,西南和远西的出勤率特别低。尽管获得认证的NF诊所的数量和在这些诊所中看望的患者数量有所增加,但许多NF患者仍然没有去专科诊所和/或旅行很长的路程进行护理。对于成年人,病情较罕见的患者和美国西部的患者而言,获得地理护理的机会更加有限。我们讨论了改善患有NF和其他罕见疾病的人获得特殊护理的潜在措施。

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