Ingrid Stacey, Yolande Knight, Claire MX Ong, Amy Lee, Suresh Karuppannan, Allison Christou, Judith M Katzenellenbogen
{"title":"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。","authors":"Ingrid Stacey, Yolande Knight, Claire MX Ong, Amy Lee, Suresh Karuppannan, Allison Christou, Judith M Katzenellenbogen","doi":"10.5694/mja2.52477","DOIUrl":null,"url":null,"abstract":"<p>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.<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. The median age for cases of unnotified RHD was higher than for notified cases (68 years; interquartile range [IQR], 42–77 years <i>v</i> 30 years; IQR, 15–49 years), and a larger proportion involved non-Indigenous people (14 of 24, 58% <i>v</i> one of 12, 8%). The proportions of people with specialist referrals (18 of 25, 72% <i>v</i> 3 of 8, 38%) and people who had commenced secondary prophylaxis (21 of 25, 84% <i>v</i> 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% <i>v</i> 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.</p><p>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.<span><sup>5</sup></span> 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.<span><sup>2, 3, 7</sup></span></p><p>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.</p><p>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.</p><p>No relevant disclosures.</p>","PeriodicalId":18214,"journal":{"name":"Medical Journal of Australia","volume":"221 9","pages":"493-494"},"PeriodicalIF":6.7000,"publicationDate":"2024-10-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.5694/mja2.52477","citationCount":"0","resultStr":"{\"title\":\"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\",\"authors\":\"Ingrid Stacey, Yolande Knight, Claire MX Ong, Amy Lee, Suresh Karuppannan, Allison Christou, Judith M Katzenellenbogen\",\"doi\":\"10.5694/mja2.52477\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>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.<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. The median age for cases of unnotified RHD was higher than for notified cases (68 years; interquartile range [IQR], 42–77 years <i>v</i> 30 years; IQR, 15–49 years), and a larger proportion involved non-Indigenous people (14 of 24, 58% <i>v</i> one of 12, 8%). The proportions of people with specialist referrals (18 of 25, 72% <i>v</i> 3 of 8, 38%) and people who had commenced secondary prophylaxis (21 of 25, 84% <i>v</i> 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% <i>v</i> 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.</p><p>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.<span><sup>5</sup></span> 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.<span><sup>2, 3, 7</sup></span></p><p>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. 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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
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.
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.