P026 Sugar rush: single-centre audit of screening and counselling for steroid-induced hyperglycaemia, based on the British Society for Rheumatology giant cell arteritis guideline

Abstract Background/Aims In patients starting steroids for giant cell arteritis (GCA), to evaluate adherence to BSR guideline: HbA1c monitoring, documentation of counselling, and detection of steroid-induced hyperglycaemia. Methods Data were gathered from the electronic medical records. Steroid-indu...

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Veröffentlicht in:Rheumatology (Oxford, England) England), 2022-04, Vol.61 (Supplement_1)
Hauptverfasser: Blackmore, Lorna J, Devine, Kirsty L, Mackie, Sarah L
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description Abstract Background/Aims In patients starting steroids for giant cell arteritis (GCA), to evaluate adherence to BSR guideline: HbA1c monitoring, documentation of counselling, and detection of steroid-induced hyperglycaemia. Methods Data were gathered from the electronic medical records. Steroid-induced hyperglycaemia was defined as new HbA1c >48 measured 3+ months after beginning steroid treatment. The data were presented at a regional meeting to raise awareness and encourage clinicians to incorporate counselling and monitoring into their practice, and a GCA clinic was set up. Practice was then re-evaluated. Results In the baseline dataset, 60 patients with GCA had a mean age of 72; 47 were female; mean body mass index (BMI) was 27 (for the 39/60 with a recorded height and weight). Mean initial dose of prednisolone was 45.9mg. The re-audit cohort were comparable with a mean age of 73.1; 19 females and mean BMI of 27 (for 15/30 with recorded). Mean initial prednisolone dose of 46.3mg. Baseline HbA1c was checked in 32/60 (53%) initially, and 28/30 (93%) on re-audit. 7/60 (12%) had documentation of counselling for steroid-induced hyperglycaemia initially, which increased to 9/30 (30%) on re-audit. Hyperglycaemia was detected in 8/60 (13%) of the initial audit group, compared to 11/30 (36%) in the re-audit. In the initial cohort, 3/10 (30%) of those with diabetes at baseline developed hyperglycaemia and 4/12 (33%) of those with pre-diabetes at baseline developed hyperglycaemia. In the re-audit, 7/9 (78%) of those with diabetes at baseline developed hyperglycaemia and 4/7 (57%) with pre-diabetes at baseline developed hyperglycaemia. Those who developed hyperglycaemia had a higher baseline weight and BMI (Table 1) in both the initial cohort and re-audit. P026 Table 1 Initial cohort Re-audit Averages and percentages Total pop. Hyperglycaemia No Hyperglycaemia Total population Hyper-glycaemia No hyper- glycaemia Total 60 8 52 30 11 19 Risk factors Age 72.3 70.6 72.6 73.1 76.5 71.1 Gender Female, n (%) 47 (78%) 06 (75%) 41 (79%) 19 (63%) 7 (64%) 12 (63%) Weight 72.1 (median = 71.7) 89.5 (median = 82.4) 70.8 (median = 70.1) 72.7 (median = 71.1) 77.5 (median = 75) 69.6 (median = 68.2) BMI 27.0 29.8 26.6 27.5 31.3 25.6 HTN n (%) 27 (45%) 2 (25%) 25 (48.1%) 16 (53%) 6(54.5%) 10 (52.6%) Smoker n (%) 15 (25%) 2 (25%) 13 (25%) 11 (36.7%) 3 (27.3%) 8 (42.1%) Raised HbA1c n (%) 22 (36.7%) 6 (75%) 15 (28.8%) 13 (43.3%) 7 (63.6%) 6 (31.6%) Fasting glucose raised n (%) 4 (1.7%
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Methods Data were gathered from the electronic medical records. Steroid-induced hyperglycaemia was defined as new HbA1c &gt;48 measured 3+ months after beginning steroid treatment. The data were presented at a regional meeting to raise awareness and encourage clinicians to incorporate counselling and monitoring into their practice, and a GCA clinic was set up. Practice was then re-evaluated. Results In the baseline dataset, 60 patients with GCA had a mean age of 72; 47 were female; mean body mass index (BMI) was 27 (for the 39/60 with a recorded height and weight). Mean initial dose of prednisolone was 45.9mg. The re-audit cohort were comparable with a mean age of 73.1; 19 females and mean BMI of 27 (for 15/30 with recorded). Mean initial prednisolone dose of 46.3mg. Baseline HbA1c was checked in 32/60 (53%) initially, and 28/30 (93%) on re-audit. 7/60 (12%) had documentation of counselling for steroid-induced hyperglycaemia initially, which increased to 9/30 (30%) on re-audit. Hyperglycaemia was detected in 8/60 (13%) of the initial audit group, compared to 11/30 (36%) in the re-audit. In the initial cohort, 3/10 (30%) of those with diabetes at baseline developed hyperglycaemia and 4/12 (33%) of those with pre-diabetes at baseline developed hyperglycaemia. In the re-audit, 7/9 (78%) of those with diabetes at baseline developed hyperglycaemia and 4/7 (57%) with pre-diabetes at baseline developed hyperglycaemia. Those who developed hyperglycaemia had a higher baseline weight and BMI (Table 1) in both the initial cohort and re-audit. P026 Table 1 Initial cohort Re-audit Averages and percentages Total pop. Hyperglycaemia No Hyperglycaemia Total population Hyper-glycaemia No hyper- glycaemia Total 60 8 52 30 11 19 Risk factors Age 72.3 70.6 72.6 73.1 76.5 71.1 Gender Female, n (%) 47 (78%) 06 (75%) 41 (79%) 19 (63%) 7 (64%) 12 (63%) Weight 72.1 (median = 71.7) 89.5 (median = 82.4) 70.8 (median = 70.1) 72.7 (median = 71.1) 77.5 (median = 75) 69.6 (median = 68.2) BMI 27.0 29.8 26.6 27.5 31.3 25.6 HTN n (%) 27 (45%) 2 (25%) 25 (48.1%) 16 (53%) 6(54.5%) 10 (52.6%) Smoker n (%) 15 (25%) 2 (25%) 13 (25%) 11 (36.7%) 3 (27.3%) 8 (42.1%) Raised HbA1c n (%) 22 (36.7%) 6 (75%) 15 (28.8%) 13 (43.3%) 7 (63.6%) 6 (31.6%) Fasting glucose raised n (%) 4 (1.7%) 1 (12.5%) 4 (7.7%) 1(3.3%) 1(9.1%) 0 (0%) Initial dose of prednisolone, mg 45.9 47.5 45.8 46.3 43.6 48.1 Screening Diabetes n (%) 10 (16.7%) 3 (37.5%) 7 (13.5%) 9 (30%) 7 (63.6%) 2 (10.5%) Pre-diabetes at baseline n (%) 1220% 450% 8 (15.4%) 7 (23.3%) 4 (36.4%) 3 (15.8%) HbA1c checked n (%) 32 (53.3%) 7 (87.5%) 25 (48.1%) 28 (93.3%) 11 (100%) 17 (89.5%) Counselled n (%) 7 (11.7%) 2 (25%) 5 (9.6%) 9 (30%) 3 (27.3%) 6 (31.6%) Conclusion The intervention improved monitoring for steroid-induced hyperglycaemia, improving detection rates. We identified patient counselling as a priority for future improvement work. Disclosure L.J. Blackmore: None. K.L. Devine: None. S.L. Mackie: Consultancies; On behalf of University of Leeds for AbbVie, AstraZeneca, Sanofi, Roche. Other; Support from Roche to attend EULAR2019.</description><identifier>ISSN: 1462-0324</identifier><identifier>EISSN: 1462-0332</identifier><identifier>DOI: 10.1093/rheumatology/keac133.025</identifier><language>eng</language><publisher>Oxford University Press</publisher><ispartof>Rheumatology (Oxford, England), 2022-04, Vol.61 (Supplement_1)</ispartof><rights>The Author(s) 2022. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For permissions, please email: journals.permissions@oup.com. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c1985-6a6afe207da6a6e918f0e01a933255fa46d8685848281b08ec0222e1306c681c3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Blackmore, Lorna J</creatorcontrib><creatorcontrib>Devine, Kirsty L</creatorcontrib><creatorcontrib>Mackie, Sarah L</creatorcontrib><title>P026 Sugar rush: single-centre audit of screening and counselling for steroid-induced hyperglycaemia, based on the British Society for Rheumatology giant cell arteritis guideline</title><title>Rheumatology (Oxford, England)</title><description>Abstract Background/Aims In patients starting steroids for giant cell arteritis (GCA), to evaluate adherence to BSR guideline: HbA1c monitoring, documentation of counselling, and detection of steroid-induced hyperglycaemia. Methods Data were gathered from the electronic medical records. Steroid-induced hyperglycaemia was defined as new HbA1c &gt;48 measured 3+ months after beginning steroid treatment. The data were presented at a regional meeting to raise awareness and encourage clinicians to incorporate counselling and monitoring into their practice, and a GCA clinic was set up. Practice was then re-evaluated. Results In the baseline dataset, 60 patients with GCA had a mean age of 72; 47 were female; mean body mass index (BMI) was 27 (for the 39/60 with a recorded height and weight). Mean initial dose of prednisolone was 45.9mg. The re-audit cohort were comparable with a mean age of 73.1; 19 females and mean BMI of 27 (for 15/30 with recorded). Mean initial prednisolone dose of 46.3mg. Baseline HbA1c was checked in 32/60 (53%) initially, and 28/30 (93%) on re-audit. 7/60 (12%) had documentation of counselling for steroid-induced hyperglycaemia initially, which increased to 9/30 (30%) on re-audit. Hyperglycaemia was detected in 8/60 (13%) of the initial audit group, compared to 11/30 (36%) in the re-audit. In the initial cohort, 3/10 (30%) of those with diabetes at baseline developed hyperglycaemia and 4/12 (33%) of those with pre-diabetes at baseline developed hyperglycaemia. In the re-audit, 7/9 (78%) of those with diabetes at baseline developed hyperglycaemia and 4/7 (57%) with pre-diabetes at baseline developed hyperglycaemia. Those who developed hyperglycaemia had a higher baseline weight and BMI (Table 1) in both the initial cohort and re-audit. P026 Table 1 Initial cohort Re-audit Averages and percentages Total pop. Hyperglycaemia No Hyperglycaemia Total population Hyper-glycaemia No hyper- glycaemia Total 60 8 52 30 11 19 Risk factors Age 72.3 70.6 72.6 73.1 76.5 71.1 Gender Female, n (%) 47 (78%) 06 (75%) 41 (79%) 19 (63%) 7 (64%) 12 (63%) Weight 72.1 (median = 71.7) 89.5 (median = 82.4) 70.8 (median = 70.1) 72.7 (median = 71.1) 77.5 (median = 75) 69.6 (median = 68.2) BMI 27.0 29.8 26.6 27.5 31.3 25.6 HTN n (%) 27 (45%) 2 (25%) 25 (48.1%) 16 (53%) 6(54.5%) 10 (52.6%) Smoker n (%) 15 (25%) 2 (25%) 13 (25%) 11 (36.7%) 3 (27.3%) 8 (42.1%) Raised HbA1c n (%) 22 (36.7%) 6 (75%) 15 (28.8%) 13 (43.3%) 7 (63.6%) 6 (31.6%) Fasting glucose raised n (%) 4 (1.7%) 1 (12.5%) 4 (7.7%) 1(3.3%) 1(9.1%) 0 (0%) Initial dose of prednisolone, mg 45.9 47.5 45.8 46.3 43.6 48.1 Screening Diabetes n (%) 10 (16.7%) 3 (37.5%) 7 (13.5%) 9 (30%) 7 (63.6%) 2 (10.5%) Pre-diabetes at baseline n (%) 1220% 450% 8 (15.4%) 7 (23.3%) 4 (36.4%) 3 (15.8%) HbA1c checked n (%) 32 (53.3%) 7 (87.5%) 25 (48.1%) 28 (93.3%) 11 (100%) 17 (89.5%) Counselled n (%) 7 (11.7%) 2 (25%) 5 (9.6%) 9 (30%) 3 (27.3%) 6 (31.6%) Conclusion The intervention improved monitoring for steroid-induced hyperglycaemia, improving detection rates. We identified patient counselling as a priority for future improvement work. Disclosure L.J. Blackmore: None. K.L. Devine: None. S.L. Mackie: Consultancies; On behalf of University of Leeds for AbbVie, AstraZeneca, Sanofi, Roche. 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Methods Data were gathered from the electronic medical records. Steroid-induced hyperglycaemia was defined as new HbA1c &gt;48 measured 3+ months after beginning steroid treatment. The data were presented at a regional meeting to raise awareness and encourage clinicians to incorporate counselling and monitoring into their practice, and a GCA clinic was set up. Practice was then re-evaluated. Results In the baseline dataset, 60 patients with GCA had a mean age of 72; 47 were female; mean body mass index (BMI) was 27 (for the 39/60 with a recorded height and weight). Mean initial dose of prednisolone was 45.9mg. The re-audit cohort were comparable with a mean age of 73.1; 19 females and mean BMI of 27 (for 15/30 with recorded). Mean initial prednisolone dose of 46.3mg. Baseline HbA1c was checked in 32/60 (53%) initially, and 28/30 (93%) on re-audit. 7/60 (12%) had documentation of counselling for steroid-induced hyperglycaemia initially, which increased to 9/30 (30%) on re-audit. Hyperglycaemia was detected in 8/60 (13%) of the initial audit group, compared to 11/30 (36%) in the re-audit. In the initial cohort, 3/10 (30%) of those with diabetes at baseline developed hyperglycaemia and 4/12 (33%) of those with pre-diabetes at baseline developed hyperglycaemia. In the re-audit, 7/9 (78%) of those with diabetes at baseline developed hyperglycaemia and 4/7 (57%) with pre-diabetes at baseline developed hyperglycaemia. Those who developed hyperglycaemia had a higher baseline weight and BMI (Table 1) in both the initial cohort and re-audit. P026 Table 1 Initial cohort Re-audit Averages and percentages Total pop. Hyperglycaemia No Hyperglycaemia Total population Hyper-glycaemia No hyper- glycaemia Total 60 8 52 30 11 19 Risk factors Age 72.3 70.6 72.6 73.1 76.5 71.1 Gender Female, n (%) 47 (78%) 06 (75%) 41 (79%) 19 (63%) 7 (64%) 12 (63%) Weight 72.1 (median = 71.7) 89.5 (median = 82.4) 70.8 (median = 70.1) 72.7 (median = 71.1) 77.5 (median = 75) 69.6 (median = 68.2) BMI 27.0 29.8 26.6 27.5 31.3 25.6 HTN n (%) 27 (45%) 2 (25%) 25 (48.1%) 16 (53%) 6(54.5%) 10 (52.6%) Smoker n (%) 15 (25%) 2 (25%) 13 (25%) 11 (36.7%) 3 (27.3%) 8 (42.1%) Raised HbA1c n (%) 22 (36.7%) 6 (75%) 15 (28.8%) 13 (43.3%) 7 (63.6%) 6 (31.6%) Fasting glucose raised n (%) 4 (1.7%) 1 (12.5%) 4 (7.7%) 1(3.3%) 1(9.1%) 0 (0%) Initial dose of prednisolone, mg 45.9 47.5 45.8 46.3 43.6 48.1 Screening Diabetes n (%) 10 (16.7%) 3 (37.5%) 7 (13.5%) 9 (30%) 7 (63.6%) 2 (10.5%) Pre-diabetes at baseline n (%) 1220% 450% 8 (15.4%) 7 (23.3%) 4 (36.4%) 3 (15.8%) HbA1c checked n (%) 32 (53.3%) 7 (87.5%) 25 (48.1%) 28 (93.3%) 11 (100%) 17 (89.5%) Counselled n (%) 7 (11.7%) 2 (25%) 5 (9.6%) 9 (30%) 3 (27.3%) 6 (31.6%) Conclusion The intervention improved monitoring for steroid-induced hyperglycaemia, improving detection rates. We identified patient counselling as a priority for future improvement work. Disclosure L.J. Blackmore: None. K.L. Devine: None. S.L. Mackie: Consultancies; On behalf of University of Leeds for AbbVie, AstraZeneca, Sanofi, Roche. Other; Support from Roche to attend EULAR2019.</abstract><pub>Oxford University Press</pub><doi>10.1093/rheumatology/keac133.025</doi><oa>free_for_read</oa></addata></record>
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title P026 Sugar rush: single-centre audit of screening and counselling for steroid-induced hyperglycaemia, based on the British Society for Rheumatology giant cell arteritis guideline
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