The RhMAT is currently being used within a clinical setting. Results indicate that a pharmacist can implement this tool in an outpatient clinic setting, taking an average of 15 minutes to complete, to capture pharmaceutical care issues and pharmacotherapy gaps within the management of patients with RA. The RhMAT was implemented for use in a sample population of 78 patients with RA and run twice at approximately 12-month intervals. The total adherence rate achieved at baseline was 81.7%. This further increased to 85.2% at 12 months, giving a statistically significant rise (Wilcoxon signed rank test p value <0.05). Therefore, following the identification of gaps through the RhMAT at baseline, the pharmacist was able to clinically discuss these gaps, which resulted in improved adherence.
Conclusion
The innovative RhMAT is a tool that uses evidence-based guidelines specific for RA. The tool is practical for use in a clinical setting within a pharmaceutical care model. The major clinical contributions of the RhMAT are its ability to detect the degree of adherence of each individual patient’s pharmacotherapy plan to evidence-based guidelines and its ability to pinpoint the actual gaps leading to the degree of and identified non-adherence. Therefore, the RhMAT can be used to close off gaps and improve the quality-of-care service offered to patients, enhancing patient safety and quality of life.
Louise Grech, BPharm (Hons), MPhil, MRPharmS, is senior clinical pharmacist in the Clinical Pharmacy Practice Unit at Mater Dei Hospital and an assistant lecturer in the Department of Pharmacy, Faculty of Medicine & Surgery at the University of Malta.
Victor Ferrito, BSc, MSc, PhD, CSci, is a professor in the Department of Pharmacy, Faculty of Medicine & Surgery at the University of Malta.
Liberato Camilleri, BEd, MSc, PhD, is an associate professor and head of the Department of Statistics and Operations Research, Faculty of Science at the University of Malta.
Anthony Serracino Inglott, BPharm, PharmD, MRPharmS, is a professor in the Department of Pharmacy, Faculty of Medicine & Surgery, University of Malta.
Lilian M. Azzopardi, BPharm (Hons), MPhil, PhD, MRPharmS, is head of the Department of Pharmacy, Faculty of Medicine & Surgery at the University of Malta.
References
- Cross M, Smith E, Hoy D, et al. The global burden of rheumatoid arthritis: Estimates from the Global Burden of Disease 2010 study. Ann Rheum Dis. Jul;2014;73(7):1316–1322.
- Cutolo M, Kitas GD, van Riel PL. Burden of disease in treated rheumatoid arthritis patients: Going beyond the joint. Semin Arthritis Rheum. 2014 Feb;43(4):479–488.
- Bijlsma JW. Optimal treatment of rheumatoid arthritis: EULAR recommendations for clinical practice. Pol Arch Med Wewn. 2010 Sept;120(9):347–353.
- Smolen JS, Landewé R, Breedveld FC, et al. EULAR recommendations for the management of rheumatoid arthritis with synthetic and biological disease-modifying antirheumatic drugs: 2013 update. Ann Rheum Dis. 2014 Mar;73(3):492–509.
- Smolen JS, Aletaha D, Bijlsmsa JW, et al. Treating rheumatoid arthritis to target: Recommendations of an international task force. Ann Rheum Dis. 2010 Apr;69(4):631–637.
- Lapadula G, Ferraccioli GF. Biosimilars in rheumatology: Pharmacological and pharmacoeconomic issues. Clin Exp Rheumatol. 2012 Jul-Aug;30(4 supp 73): S102–S106.
- Dörner T, Strand V, Castañeda-Hernandez G, et al. The role of biosimilars in the treatment of rheumatic diseases. Ann Rheum Dis. 2013 Mar;72(3):322–328.
- Brodszky V, Baji P, Balogh O, Péntek M. Budget impact analysis of biosimilar infliximab (CT-P13) for the treatment of rheumatoid arthritis in six Central and Eastern European countries. Eur J Health Econ. 2014 May; 15 Suppl 1:S65–S71.
- Fries JF. Current treatment paradigms in rheumatoid arthritis. Rheumatology (Oxford). 2000 Jun;39 Suppl 1:30–35.
- Parkinson S, Alldred A. Drug regimens for rheumatoid arthritis. Hospital Pharmacist. 2002;9:11–15.
- American College of Rheumatology Subcommittee on Rheumatoid Arthritis Guidelines. Guidelines for management of rheumatoid arthritis: 2002 update. Arthritis Rheum. 2002 Feb;46(2):328–346.
- McInness IB, Schett G. The pathogenesis of rheumatoid arthritis. N Eng J Med. 2011 Dec 8;365(23): 2205–2219.
- Smolen JS, Aletaha D, Koeller M, Weisman MH, Emery P. New therapies for treatment of rheumatoid arthritis. Lancet. 2007 Dec 1;370(9602):1861–1874.
- Schuna AA, Megeff C. New drugs for the treatment of rheumatoid arthritis. Am J Health Syst Pharm. 2000 Feb 1;57(3):225–234.
- Tak PP, Kalden JR. Advances in rheumatology: new targeted therapeutics. Arthritis Res Ther. 2011 May 25;13 Suppl 1:S5.
- Selmi C, Generali E, Massarotti M, et al. New treatments for inflammatory rheumatic disease. Immunol Res. 2014 Dec:60(2-3): 277–288.
- Eaton AT, Davis PN, Ndefo UA, Ebiogwu A. Update on pharmacotherapeutic options for rheumatoid arthritis. US Pharmacist. 2013 Oct;38(10):44–48.
- Kumar P, Banik S. Pharmacotherapy options in rheumatoid arthritis. Clin Med Insights: Arthritis Musculoskelet Disord. 2013 Aug;6:35–43.
- Jansen JP, Buckley F, Dejonckheere F, Ogale S. Comparative efficacy of biologics as monotherapy and in combination with methotrexate on patient reported outcomes (PROs) in rheumatoid arthritis patients with an inadequate response to conventional DMARDs—A systematic review and network meta-analysis. Health Qual Life Outcomes. 2014 Jul 3;12:102.
- Singh JA, Furst DE, Bharat A, et al. 2012 update of the 2008 American College of Rheumatology recommendations for the use of disease-modifying antirheumatic drugs and biologic agents in the treatment of rheumatoid arthritis. Arthritis Care Res. 2012 May;64(5):625–639.
- Ding T, Ledingham J, Luqmani R, et al. BSR and BHPR rheumatoid arthritis guidelines on safety of anti-TNF therapies. Rheumatology (Oxford). 2010 Nov;49(11):2217–2219.
- Woodrick RS, Ruderman EM. Safety of biologic therapy in rheumatoid arthritis. Nat Rev Rheumatol. 2011 Oct 11;7(11):639–652.
- Rubbert-Roth A. Assessing the safety of biologic agents in patients with rheumatoid arthritis. Rheumatology (Oxford). 2012 Jul;51 Suppl 5:v38–v47.
- Ramiro S, Gaujoux-Viala C, Nam JL, et al. Safety of synthetic and biological DMARDs: A systematic literature review informing the 2013 update of the EULAR recommendations for management of rheumatoid arthritis. Ann Rheum Dis. 2014 Mar;73(3):529–535.
- Mota LM, Cruz BA, Brenol CV, et al. [Safe use of biological therapies for the treatment of rheumatoid arthritis and spondyloarthritides] [article in Portuguese]. Rev Bras Reumatol. 2015 May–Jun;55(3):281–309.
- Uhlig T, Moe RH, Kvien TK. The burden of disease in rheumatoid arthritis. Pharmacoeconomics. 2014 Sep;32(9):841–851.
- Stephens S, Botteman MF, Cifaldi MA, van Hout BA. Modelling the cost-effectiveness of combination therapy for early, rapidly progressing rheumatoid arthritis by simulating the reversible and irreversible effects of the disease. BMJ Open. 2015 Jun 9;5(6):e006560.
- Farfan-Portet MI, Gerkens S, Lepage-Nefkens I, et al. Are biosimilars the next tool to guarantee cost-containment for pharmaceutical expenditures? Eur J Health Econ. 2014 Apr;15(3):223–228.
- Flick C, Farrell J. The role of the pharmacist in the management of rheumatic disease. The Rheumatologist. 2013 Aug;7(8).
- Hudson S, Bayraktar A, McAnaw J. Pharmaceutical care issues in the management of rheumatoid arthritis. Int J Adv Rheumatol. 2003;1(3):97–103.
- Griscti S, Serracino-Inglott A, Zarb-Adami M, et al. Management of rheumatoid arthritis. Hosp Pharm Europe. 2010 Mar/Apr (updated March 23, 2010).
- Grech L, Coleiro B, Borg A, et al. Evaluation of the impact of a pharmaceutical care service offered to rheumatoid arthritis patients within an ambulatory setting. Am J Pharm Health Res. 2013 Jul;1(7):78–86.
- Bornstein C, Craig M, Tin D. Practice guidelines for pharmacists: The pharmacological management of rheumatoid arthritis with traditional and biologic disease-modifying antirheumatic drugs. Can Pharm J. 2014 Mar;147(2):97–109.
- Gong L, Wooley MC, Glasser CE, et al. Rheumatoid arthritis: Aggressive new treatment guidelines. US Pharm. 2014;39(11 Specialty & Oncology suppl):3–7.
- McAnaw J, Hudson S, McGlynn S. Development of an evidence-based medication assessment tools to demonstrate the quality of drug therapy use in patients with heart failure. Int J Pharm Practice. 2003 Sep;11:R17.
- Garcia B, Smabrekke L, Trovik T, Giverhaug T. Application of the MAT-CHDSP to assess guideline adherence and therapy goal achievement in secondary prevention of coronary heart disease after percutaneous coronary intervention. Eur J Clin Pharmacol. 2013 Mar;69(3):703–709.
- Dreischulte T, Johnson J, McAnaw J, et al. Medication assessment tool to detect care issues from routine data: A pilot study in primary care. Int J Clin Pharm. 2013 Dec;35(6):1063–1074.
- Issam Diab M, Julienne Johnson J, Hudson S. Adherence to clinical guidelines in management of diabetes and prevention of cardiovascular disease in Qatar. Int J Clin Pharm. 2013 Feb;35(1):101–112.
- Håkonsen GD, Strelec P, Campbell D, et al. Adherence to medication guideline criteria in pain management. J Pain Symptom Manage. 2009 Jun;37(6):1006–1018.
- Liu HP, Chen HY, Johnson J, Lin YM. A medication assessment tool to evaluate adherence to medication guideline in asthmatic children. Int J Clin Pharm. 2013 Apr;35(2):289–295.