Disease-modifying drugs, multiple sclerosis and infection-related healthcare use in British Columbia, Canada: a population-based study

被引:0
作者
Graf, Jonas [1 ,2 ]
Ng, Huah Shin [1 ,2 ,3 ]
Zhu, Feng [1 ,2 ]
Zhao, Yinshan [1 ,2 ]
Wijnands, Jose M. A. [1 ,2 ]
Evans, Charity [4 ]
Fisk, John D. [5 ,6 ,7 ,8 ,9 ]
Marrie, Ruth Ann [10 ,11 ]
Tremlett, Helen [1 ,2 ,12 ]
机构
[1] Univ British Columbia, Dept Med, Div Neurol, Vancouver, BC, Canada
[2] Univ British Columbia, Djavad Mowafaghian Ctr Brain Hlth, Vancouver, BC, Canada
[3] Flinders Univ S Australia, Flinders Hlth & Med Res Inst, Coll Med & Publ Hlth, Bedford Pk, SA, Australia
[4] Univ Saskatchewan, Coll Pharm & Nutr, Saskatoon, SK, Canada
[5] Dalhousie Univ, Nova Scotia Hlth Author, Halifax, NS, Canada
[6] Dalhousie Univ, Dept Psychiat, Halifax, NS, Canada
[7] Dalhousie Univ, Dept Psychol, Halifax, NS, Canada
[8] Dalhousie Univ, Dept Neurosci, Halifax, NS, Canada
[9] Dalhousie Univ, Dept Med, Halifax, NS, Canada
[10] Univ Manitoba, Rady Fac Hlth Sci, Dept Internal Med, Max Rady Coll Med, Winnipeg, MB, Canada
[11] Univ Manitoba, Max Rady Coll Med, Rady Fac Hlth Sci, Dept Community Hlth Sci, Winnipeg, MB, Canada
[12] Univ British Columbia, UBC Hosp, Djavad Mowafaghian Ctr Brain Hlth Fac Med Neurol r, Djavad Mowafaghian Ctr Brain Hlth,Fac Med Neurol R, 2211 Wesbrook Mall, Vancouver, BC V6T 2B5, Canada
来源
LANCET REGIONAL HEALTH-AMERICAS | 2024年 / 29卷
基金
加拿大健康研究院;
关键词
Multiple sclerosis; Disease-modifying drugs; Infections; Healthcare use; INTERFERON-BETA; NATURAL-HISTORY; PREVALENCE; RISK; COMORBIDITIES; TYPE-1;
D O I
10.1016/j.lana.2023.100667
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Background Much remains unknown surrounding the disease -modifying drugs (DMDs) used to treat multiple sclerosis and infection -related healthcare use in the 'real -world' setting. We examined if DMD exposure was associated with altered infection -related healthcare use. Methods We assessed if DMD (versus no) exposure was associated with altered infection -related hospitalizations, physician claims, and prescriptions filled in British Columbia, Canada (1996-2017). Healthcare use was assessed using negative binomial and proportional means regression models, reported as sex-/age-/comorbidity-/calendar year -/socioeconomic -adjusted rate and hazard ratios [aRR, aHR], with 95% confidence intervals [CIs]). Findings We identified 19,360 multiple sclerosis cases (13,940/19,360; 72.0% women; mean age at study start = 44.5 standard deviation, SD = 13.3; mean follow-up = 11.7 [SD = 7.3] years). Relative to unexposed periods, exposure to any DMD was associated with a lower infection -related rate of physician claims (aRR = 0.88; 95% CI:0.85-0.92) and hazard of hospitalization (aHR = 0.64; 95% CI:0.56-0.73), and a higher rate of infection -related prescriptions (aRR = 1.14; 95% CI:1.08-1.20). Exposure to any injectable or oral DMD was associated with a lower infectionrelated rate of physician claims (injectable aRR = 0.88; 95% CI:0.84-0.92, oral aRR = 0.83; 95% CI:0.77-0.90) and hazard of hospitalization (injectable aHR = 0.65; 95% CI:0.56-0.75, oral aHR = 0.54; 95% CI:0.38-0.77), whereas intravenous DMD exposure was not (aRR = 0.99; 95% CI:0.86-1.14, aHR = 0.73; 95% CI:0.49-1.09). Exposure to any injectable or intravenous DMD was associated with a higher rate of infection -related prescriptions (injectable aRR = 1.15; 95% CI:1.08-1.22, intravenous = 1.34; 95% CI:1.15-1.56), whereas oral DMDs were not (aRR = 0.98; 95% CI:0.91-1.05). Interpretation DMD exposure for the treatment of MS was associated with differences in infection -related healthcare use. While infection -related hospitalizations and physician visits were lower, prescription fills were higher. How these differences in infection -related healthcare use affect outcomes in persons with multiple sclerosis warrants consideration.
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页数:13
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