Tikka Theofano, Webb Joanne, Agostini Paula, Kerr Amy, Mannion Glenn, Steyn Richard S, Bishay Ehab, Kalkat Maninder S, Rajesh Pala B, Naidu Babu
Department of Thoracic Surgery, Heart of England NHS Foundation Trust, Bordesley Green East, Birmingham, UK.
College of Medical and Dental Sciences, University of Birmingham, Edgbaston, Birmingham, UK.
J Cardiothorac Surg. 2016 Apr 26;11(1):69. doi: 10.1186/s13019-016-0470-7.
Pectus is the most common congenital disorder. Awareness amongst primary care physicians and the general public is poor. NHS commissioning bodies plan to withdraw funding for this surgery because they deem a lack of sufficient evidence of benefit. The purpose of this study is to assess the effects of introducing a patient information website on referral and activity patterns and on patients reported outcomes.
We produced an innovative information website, www.pectus.co.uk , accessible to the general public, providing information about pectus deformities; management options and advice about surgery. Referral patterns and number of cases where studied before and after the introduction of the website in 2010. Patients' satisfaction post-op was assessed using the Brompton's single step questionnaire (SSQ).
The website had considerable traffic with 2179 hits in 2012, 4983 in 2013 and 7416 in 2014. This has led to 1421 contacts and 372 email enquiries. These emails have resulted in an increased number of patients who have been assessed and go on to have surgery. We asked 59 pectus excavatum patients who were operated from 2008 to 2014 to complete the SSQ. We received 32 replies. Eighty-four percent (16/19) of patients who visited the website and then underwent surgery, found the website useful. All patients scored satisfactorily in SSQ. Even though those who visited the website tended to be more satisfied with the surgical outcomes this did not reach statistical significance. This group of patients said that would have the operation again given the option compared to 76.9 % of the group who did not visit the website before surgery (p=0.031). Despite the fact that patients who visited the website experienced more post-operative complications were equally or more satisfied with post-operative outcomes. The overall SSQ obtainable score was not different for the two subgroups, being more widespread in the group that did not visit the website.
The introduction of a pectus patient information website has significantly improved access to specialised services. Patients are overall highly satisfied with the surgical outcomes.
漏斗胸是最常见的先天性疾病。基层医疗医生和普通公众对此病的认知度较低。英国国家医疗服务体系(NHS)的委托机构计划停止为该手术提供资金,因为他们认为缺乏足够的证据证明其益处。本研究的目的是评估引入患者信息网站对转诊和活动模式以及患者报告结局的影响。
我们制作了一个创新的信息网站www.pectus.co.uk,公众可访问,提供有关漏斗胸畸形、治疗选择和手术建议的信息。在2010年网站推出前后,对转诊模式和病例数量进行了研究。使用布朗普顿单步问卷(SSQ)评估患者术后满意度。
该网站流量可观,2012年有2179次点击,2013年有4983次,2014年有7416次。这导致了1421次联系和372次电子邮件咨询。这些电子邮件使接受评估并继而接受手术的患者数量增加。我们邀请了59名在2008年至2014年接受手术的漏斗胸患者填写SSQ。我们收到了32份回复。84%(16/19)访问网站后接受手术的患者认为该网站有用。所有患者在SSQ中的得分均令人满意。尽管访问网站的患者往往对手术结果更满意,但这未达到统计学显著性。与76.9%术前未访问网站的患者相比,这组患者表示若有选择会再次接受手术(p = 0.031)。尽管访问网站的患者术后并发症更多,但他们对术后结局同样满意或更满意。两个亚组的总体SSQ可获得分数没有差异,在未访问网站的组中分布更广泛。
引入漏斗胸患者信息网站显著改善了获得专科服务的机会。患者总体上对手术结果高度满意。