Notification of acute rheumatic fever and rheumatic heart disease in hospitalised people in the Midwest region of Western Australia, 2012–2022: retrospective administrative data analysis

IF 6.7 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL Medical Journal of Australia Pub Date : 2024-10-04 DOI:10.5694/mja2.52477
Ingrid Stacey, Yolande Knight, Claire MX Ong, Amy Lee, Suresh Karuppannan, Allison Christou, Judith M Katzenellenbogen
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Their prevalence is much higher among First Nations people than other Australians.<span><sup>1</sup></span> Treatment guidelines recommend that people with ARF or RHD be hospitalised (RHD) and notified to jurisdictional RHD registers (ARF, RHD); early diagnosis is associated with better clinical outcomes.<span><sup>2, 3</sup></span></p><p>In Western Australia, the notification by clinicians of new ARF and RHD diagnoses has been mandatory since 2009 and 2015 respectively.<span><sup>2, 4</sup></span> WA RHD Register staff record demographic and clinical details for each case, and commence recall and reminder services for people with ARF or RHD. For people who are hospitalised, clinical coders enter discharge summary information into the WA Hospital Morbidity Data System (HMDS), using International Classification of Diseases, tenth revision, Australian modification (ICD-10-AM) codes (ARF: I00–I02; RHD: I05–I09). The register should also be notified of any person hospitalised with ARF or RHD. In 2020, we estimated that 54% of cases of RHD in First Nations people and 99% of cases in non-Indigenous people in WA were not recorded in the register, but no person-identifiable regional analyses or validation studies have been undertaken.<span><sup>5</sup></span></p><p>For our retrospective administrative data analysis, we validated ARF and RHD hospitalisations in the remote Midwest region of WA, calculated RHD register notification rates, and examined demographic and clinical factors associated with notification. [Correction added on 9 October 2024, after first online publication: this sentence has been corrected.] All hospitalisations with ARF or RHD in the Midwest region during 1 May 2012 – 30 April 2022 were identified in the HMDS. Medical records for the admissions were requested (including discharge summaries, pathology results, specialist reports, emergency presentation and inpatient paper medical records), reviewed, and validated by resident medical officers, with cardiologist support as required. Records that could not be obtained or which indicated that the case did not meet the criteria for possible, probable, or confirmed diagnosis of ARF or RHD<span><sup>2</sup></span> were excluded. First Nations people were identified from information in clinical notes in paper medical records and hospital admission records (in which Indigenous status is self-reported or recorded by the clinician).</p><p>The study was approved by the Western Australian Aboriginal Health Ethics Committee (project reference 717), the WA Health Department (2016/29), and the WA Country Health Service Human Research Ethics Committee (2022.14). First Nations oversight and governance of the parent project for this study (End RHD in Australia: Study of Epidemiology, ERASE<span><sup>6</sup></span>) was provided by First Nations chief investigators. We regularly communicate ERASE findings, prior to their publication, to the National Aboriginal Community Controlled Health Organisation and the Aboriginal Health Council of Western Australia.</p><p>Records for 69 people (confirmed ARF, 33; confirmed RHD, 36) were cross-referenced with the RHD register to determine notification status (Box 1). The small number precluded formal statistical comparisons. Twenty-five of 33 ARF cases and twelve of 36 RHD cases had been notified to the register. Thirty of the ARF cases and 28 of the RHD cases had been diagnosed during 2015–2022; 31 of 33 people with ARF and 21 of 36 with RHD were First Nations people. 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引用次数: 0

Abstract

Acute rheumatic fever (ARF) and rheumatic heart disease (RHD) are caused by untreated group A streptococcus infections. Their prevalence is much higher among First Nations people than other Australians.1 Treatment guidelines recommend that people with ARF or RHD be hospitalised (RHD) and notified to jurisdictional RHD registers (ARF, RHD); early diagnosis is associated with better clinical outcomes.2, 3

In Western Australia, the notification by clinicians of new ARF and RHD diagnoses has been mandatory since 2009 and 2015 respectively.2, 4 WA RHD Register staff record demographic and clinical details for each case, and commence recall and reminder services for people with ARF or RHD. For people who are hospitalised, clinical coders enter discharge summary information into the WA Hospital Morbidity Data System (HMDS), using International Classification of Diseases, tenth revision, Australian modification (ICD-10-AM) codes (ARF: I00–I02; RHD: I05–I09). The register should also be notified of any person hospitalised with ARF or RHD. In 2020, we estimated that 54% of cases of RHD in First Nations people and 99% of cases in non-Indigenous people in WA were not recorded in the register, but no person-identifiable regional analyses or validation studies have been undertaken.5

For our retrospective administrative data analysis, we validated ARF and RHD hospitalisations in the remote Midwest region of WA, calculated RHD register notification rates, and examined demographic and clinical factors associated with notification. [Correction added on 9 October 2024, after first online publication: this sentence has been corrected.] All hospitalisations with ARF or RHD in the Midwest region during 1 May 2012 – 30 April 2022 were identified in the HMDS. Medical records for the admissions were requested (including discharge summaries, pathology results, specialist reports, emergency presentation and inpatient paper medical records), reviewed, and validated by resident medical officers, with cardiologist support as required. Records that could not be obtained or which indicated that the case did not meet the criteria for possible, probable, or confirmed diagnosis of ARF or RHD2 were excluded. First Nations people were identified from information in clinical notes in paper medical records and hospital admission records (in which Indigenous status is self-reported or recorded by the clinician).

The study was approved by the Western Australian Aboriginal Health Ethics Committee (project reference 717), the WA Health Department (2016/29), and the WA Country Health Service Human Research Ethics Committee (2022.14). First Nations oversight and governance of the parent project for this study (End RHD in Australia: Study of Epidemiology, ERASE6) was provided by First Nations chief investigators. We regularly communicate ERASE findings, prior to their publication, to the National Aboriginal Community Controlled Health Organisation and the Aboriginal Health Council of Western Australia.

Records for 69 people (confirmed ARF, 33; confirmed RHD, 36) were cross-referenced with the RHD register to determine notification status (Box 1). The small number precluded formal statistical comparisons. Twenty-five of 33 ARF cases and twelve of 36 RHD cases had been notified to the register. Thirty of the ARF cases and 28 of the RHD cases had been diagnosed during 2015–2022; 31 of 33 people with ARF and 21 of 36 with RHD were First Nations people. The median age for cases of unnotified RHD was higher than for notified cases (68 years; interquartile range [IQR], 42–77 years v 30 years; IQR, 15–49 years), and a larger proportion involved non-Indigenous people (14 of 24, 58% v one of 12, 8%). The proportions of people with specialist referrals (18 of 25, 72% v 3 of 8, 38%) and people who had commenced secondary prophylaxis (21 of 25, 84% v 5 of 8, 63%) were larger for notified than unnotified cases of ARF. However, only 26 of 33 people with ARF had been referred for echocardiography. The clinical features of unnotified RHD were more frequently consistent with more severe disease (17 of 24, 71% v 6 of 12 notified cases, 50%) (Box 2). The WA RHD register was subsequently notified of all previously unnotified cases of ARF and RHD identified during our study.

Our study was limited to data included in the available medical records. However, WA RHD register notification rates in the Midwest region were similar to those reported elsewhere in Australia.5 ARF and RHD notification rates were higher for First Nations people, and the median age of people with notified RHD was lower. Care aligned with national treatment guidelines, more likely to achieve favourable clinical outcomes, was more frequently noted for notified than unnotified cases of ARF.2, 3, 7

People with unnotified RHD receive acute care in hospitals in the Midwest region of WA, but the non-notification rate is concerningly high (67%). People with unnotified RHD do not benefit from the monitoring and case management offered by the WA register. Notification rates in the surrounding WA regions where the burden of ARF and RHD is high (including the Pilbara and Goldfields) should also be examined. Clinician awareness of notification requirements, including for advanced disease, and automated technology that facilitates ARF and RHD notification, are needed.

Open access publishing facilitated by The University of Western Australia, as part of the Wiley – the University of Western Australia agreement via the Council of Australian University Librarians.

No relevant disclosures.

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2012-2022年西澳大利亚州中西部地区住院病人急性风湿热和风湿性心脏病的通报:一项回顾性队列研究。
急性风湿热(ARF)和风湿性心脏病(RHD)是由未经治疗的 A 组链球菌感染引起的。1 治疗指南建议,急性风湿热或风湿性心脏病患者应住院治疗(风湿性心脏病)并向辖区风湿性心脏病登记处(急性风湿热、风湿性心脏病)通报;早期诊断可获得更好的临床疗效。2, 3 在西澳大利亚州,自 2009 年和 2015 年起,临床医生必须分别通报新诊断的急性风湿热和风湿性心脏病病例。对于住院患者,临床编码人员会使用《国际疾病分类》第十版澳大利亚修订版(ICD-10-AM)代码(ARF:I00-I02;RHD:I05-I09)将出院摘要信息输入西澳大利亚州医院发病率数据系统(HMDS)。任何因急性肾功能衰竭或急性肾脏病住院的患者也应在登记册中进行通报。2020 年,我们估计西澳大利亚州 54% 的原住民和 99% 的非原住民 RHD 病例未在登记册中记录,但尚未开展可识别个人的区域分析或验证研究。5 在我们的回顾性行政数据分析中,我们验证了西澳大利亚州中西部偏远地区的 ARF 和 RHD 住院病例,计算了 RHD 登记册的通知率,并研究了与通知相关的人口和临床因素。[更正于2024年10月9日首次在线发表后:此句已更正]。中西部地区在2012年5月1日至2022年4月30日期间因急性肾功能衰竭或急性肾脏病住院的所有病例均在HMDS中进行了确认。要求住院患者提供医疗记录(包括出院摘要、病理结果、专家报告、急诊病历和住院患者纸质医疗记录),并由住院医师进行审查和验证,必要时由心脏病专家提供支持。无法获得的记录或表明病例不符合可能、疑似或确诊为急性肾功能衰竭或急性缺血性心肌病2 标准的记录均被排除在外。原住民是从纸质医疗记录和入院记录(其中土著身份由临床医生自我报告或记录)中的临床笔记信息中确定的。该研究获得了西澳大利亚原住民健康伦理委员会(项目编号 717)、西澳大利亚卫生部(2016/29)和西澳大利亚乡村卫生服务人类研究伦理委员会(2022.14)的批准。原住民首席调查员负责监督和管理本研究的母项目(End RHD in Australia: Study of Epidemiology, ERASE6)。我们定期向全国原住民社区控制健康组织(National Aboriginal Community Controlled Health Organisation)和西澳大利亚原住民健康委员会(Aboriginal Health Council of Western Australia)通报 ERASE 的研究结果,然后再将其公布于众。69 人(33 人确诊为 ARF;36 人确诊为 RHD)的记录与 RHD 登记册进行了交叉比对,以确定通知状态(方框 1)。由于人数较少,因此无法进行正式的统计比较。在 33 例急性肠胃炎病例中,有 25 例已向登记册通报;在 36 例流 感病例中,有 12 例已向登记册通报。其中,30 例急性肾功能衰竭病例和 28 例急性肾脏病病例是在 2015-2022 年期间确诊的;33 例急性肾功能衰竭患者中有 31 人是原住民,36 例急性肾脏病患者中有 21 人是原住民。未通报的 RHD 病例的中位年龄高于通报病例(68 岁;四分位数间距 [IQR] 为 42-77 岁对 30 岁;IQR 为 15-49 岁),非原住民患者的比例更高(24 例中有 14 例,占 58% ;12 例中有 1 例,占 8% )。与未通报的 ARF 病例相比,已通报的 ARF 病例中由专家转诊的比例(25 例中的 18 例,72% 对 8 例中的 3 例,38%)和已开始二级预防治疗的比例(25 例中的 21 例,84% 对 8 例中的 5 例,63%)更高。然而,在 33 名 ARF 患者中,只有 26 人被转诊进行了超声心动图检查。未通报的急性心肌梗死病例的临床特征往往与更严重的疾病相符(24 例中的 17 例,71% 对 12 例通报病例中的 6 例,50%)(方框 2)。我们的研究仅限于现有医疗记录中包含的数据。然而,中西部地区的西澳大利亚州狂犬病登记通报率与澳大利亚其他地区报告的通报率相似。5 原住民的狂犬病和狂犬病通报率较高,狂犬病患者的中位年龄较低。与未通报的 ARF 病例相比,通报的 ARF 病例更常接受符合国家治疗指南的治疗,更有可能取得良好的临床疗效。2, 3, 7未通报的 RHD 患者在西澳大利亚州中西部地区的医院接受急诊治疗,但未通报率高得令人担忧(67%)。 未通报的 RHD 患者无法从西澳大利亚登记册提供的监测和病例管理中受益。此外,还应该对西澳大利亚周边地区(包括皮尔巴拉和金地地区)的通报率进行检查,因为这些地区的急性肾功能衰竭和急性肾脏病发病率较高。临床医生需要了解通报要求,包括晚期疾病的通报要求,以及有助于ARF和RHD通报的自动化技术。
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来源期刊
Medical Journal of Australia
Medical Journal of Australia 医学-医学:内科
CiteScore
9.40
自引率
5.30%
发文量
410
审稿时长
3-8 weeks
期刊介绍: The Medical Journal of Australia (MJA) stands as Australia's foremost general medical journal, leading the dissemination of high-quality research and commentary to shape health policy and influence medical practices within the country. Under the leadership of Professor Virginia Barbour, the expert editorial team at MJA is dedicated to providing authors with a constructive and collaborative peer-review and publication process. Established in 1914, the MJA has evolved into a modern journal that upholds its founding values, maintaining a commitment to supporting the medical profession by delivering high-quality and pertinent information essential to medical practice.
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