PMID- 33938498 OWN - NLM STAT- MEDLINE DCOM- 20211125 LR - 20230927 IS - 1536-7355 (Electronic) IS - 1076-1608 (Linking) VI - 27 IP - 8 DP - 2021 Dec 1 TI - An Initiative to Improve Timely Glucocorticoid Tapering in Vasculitis. PG - e612-e615 LID - 10.1097/RHU.0000000000001744 [doi] AB - BACKGROUND/OBJECTIVE: High-dose glucocorticoids (GCs) are required in the initial treatment of systemic vasculitis. However, slow or delayed tapering can lead to unnecessary GC exposure and toxicity. In this quality improvement initiative, we aimed to increase appropriate GC tapering among newly referred patients awaiting specialty consultation at a tertiary vasculitis clinic. METHODS: For each patient referred for anti-neutrophil cytoplasm antibody-associated vasculitis (AAV) or large vessel vasculitis (LVV), recommendation-based GC tapering suggestions were faxed to referring physicians. To maximize uptake, the intervention format was modified according to feedback from referring physicians' offices. The proportion of new patients presenting to their first appointment who (1) had started to taper GCs, (2) were taking their target GC dose according to recommendations, (3) experienced a vasculitis flare during tapering were compared before (July 2017-January 2019) and after (February-October 2019) the intervention. RESULTS: Among 169 consecutive patients referred for AAV or LVV, the proportion who had started to taper GCs by their first visit increased from 84 of 117 (72%) preintervention to 49 of 52 (94%) postintervention (p < 0.01). Mean daily prednisone dose at first visit decreased from 29.9 (SD, 18) mg to 21.7 (SD, 14) mg (p < 0.01). However, the proportion who were ultimately taking "target" GC doses at their first visit did not significantly increase (72% vs. 77%). Disease flares during tapering were similar before and after the intervention (9% vs. 12%). CONCLUSIONS: Patients with AAV and LVV had increased GC tapering and lower GC doses at first visit following a preappointment intervention. Further strategies are needed to improve timely GC tapering in vasculitis. CI - Copyright (c) 2021 Wolters Kluwer Health, Inc. All rights reserved. FAU - Mendel, Arielle AU - Mendel A AD - From the Lupus and Vasculitis Clinic, Division of Rheumatology, McGill University Health Centre, Montreal, Quebec. FAU - Ennis, Daniel AU - Ennis D AD - Division of Rheumatology, Vancouver General Hospital, Vancouver, British Columbia. FAU - Lake, Shirley AU - Lake S AD - Division of Rheumatology, Sunnybrook Health Sciences Centre. FAU - Carette, Simon AU - Carette S AD - Vasculitis Clinic, Division of Rheumatology, Mount Sinai Hospital, Toronto, Ontario, Canada. FAU - Pagnoux, Christian AU - Pagnoux C AD - Vasculitis Clinic, Division of Rheumatology, Mount Sinai Hospital, Toronto, Ontario, Canada. LA - eng PT - Journal Article PL - United States TA - J Clin Rheumatol JT - Journal of clinical rheumatology : practical reports on rheumatic & musculoskeletal diseases JID - 9518034 RN - 0 (Glucocorticoids) RN - VB0R961HZT (Prednisone) SB - IM MH - *Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis/drug therapy MH - *Arteritis MH - Glucocorticoids MH - Humans MH - Prednisone MH - Treatment Outcome COIS- The authors declare no conflict of interest. EDAT- 2021/05/04 06:00 MHDA- 2021/11/26 06:00 CRDT- 2021/05/03 09:15 PHST- 2021/05/04 06:00 [pubmed] PHST- 2021/11/26 06:00 [medline] PHST- 2021/05/03 09:15 [entrez] AID - 00124743-202112000-00060 [pii] AID - 10.1097/RHU.0000000000001744 [doi] PST - ppublish SO - J Clin Rheumatol. 2021 Dec 1;27(8):e612-e615. doi: 10.1097/RHU.0000000000001744.