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dc.contributor.authorHamarneh, Y.
dc.contributor.authorCharrois, Theresa
dc.contributor.authorLewanczuk, R.
dc.contributor.authorTsuyuki, R.
dc.date.accessioned2017-01-30T12:44:19Z
dc.date.available2017-01-30T12:44:19Z
dc.date.created2013-10-09T20:00:36Z
dc.date.issued2013
dc.identifier.citationHamarneh, Yazid N. Al and Charrois, Theresa and Lewanczuk, Richard and Tsuyuki, Ross T. 2013. Pharmacist intervention for glycaemic control in the community (the RxING study). BMJ Open. 3 (9): e003154
dc.identifier.urihttp://hdl.handle.net/20.500.11937/24648
dc.identifier.doi10.1136/bmjopen-2013-003154
dc.description.abstract

OBJECTIVE: To determine the effect of a community pharmacist prescribing intervention on glycaemic control in patients with poorly controlled type 2 diabetes. DESIGN: Pragmatic, before–after design. SETTING: 12 community pharmacies in Alberta, Canada. PARTICIPANTS: Type 2 diabetes receiving oral hypoglycaemic medications and with glycated haemoglobin (HbA1c) of 7.5–11%.INTERVENTION: Pharmacists systematically identified potential candidates by inviting patients with type 2 diabetes to test their HbA1c using validated point-of-care technology. Pharmacists prescribed 10 units of insulin glargine at bedtime, adjusted by increments of 1 unit daily to achieve a morning fasting glucose of ≤5.5 mmol/L. The patients were followed up at 2, 4, 8, 14, 20 and 26 weeks. PRIMARY OUTCOME: Change in HbA1c from baseline to week 26. SECONDARY OUTCOMES: Proportion of patients achieving target HbA1c, changes in oral hypoglycaemic agents, quality of life and patient satisfaction, persistence on insulin glargine, number of insulin dosage adjustments per patient and number of hypoglycaemic episodes.RESULTS: We screened 365 patients of whom 111 were eligible. Of those, 100 (90%) were enrolled in the study; all 11 patients who did not consent refused to use insulin. Average age was 64 years (SD 10.4), while average diabetes duration was 10.2 years (SD 7). HbA1c was reduced from 9.1% (SD 1) at baseline to 7.3% (SD 0.9); a change of 1.8% (95% CI 1.4 to 2, p<0.001). Fasting plasma glucose was reduced from 11 (SD 3.3) to 6.9 mmol/L (SD 1.8); a change of 4.1 mmol/L (95% CI of 3.3 to 5, p=0.007). Fifty-one per cent of the patients achieved the target HbA1c of ≤7% at the end of the study.CONCLUSIONS: This is the first completed study of independent prescribing by pharmacists. Our results showed similar improvements in glycaemic control as previous physician-led studies. RxING provides further evidence for the benefit of pharmacist care in diabetes.

dc.publisherB M J Group
dc.titlePharmacist intervention for glycaemic control in the community (the RxING study)
dc.typeJournal Article
dcterms.source.volume6
dcterms.source.issn2044-6055
dcterms.source.titleBMJ Open
curtin.note

This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 3.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. http://creativecommons.org/licenses/by-nc/3.0/

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