Pan-Canadian assessment of pandemic immunization data collection: study methodology

被引:5
作者
Pereira, Jennifer A. [1 ]
Quach, Susan [1 ]
Heidebrecht, Christine [1 ]
Foisy, Julie [1 ]
Quan, Sherman [2 ,3 ]
Finkelstein, Michael [4 ]
Sikora, Christopher A. [5 ]
Bettinger, Julie A. [6 ]
Buckeridge, David L. [7 ]
McCarthy, Anne [8 ]
Deeks, Shelley [1 ]
Kwong, Jeffrey C. [1 ,2 ,9 ,10 ,11 ]
机构
[1] Ontario Agcy Hlth Protect & Promot, Toronto, ON, Canada
[2] Univ Hlth Network, Toronto, ON, Canada
[3] Ctr Innovat Complex Care, Toronto, ON, Canada
[4] Toronto Publ Hlth, Toronto, ON, Canada
[5] Univ Alberta, Sch Publ Hlth, Edmonton, AB, Canada
[6] Univ British Columbia, Vaccine Evaluat Ctr, Vancouver, BC V5Z 1M9, Canada
[7] McGill Univ, Montreal, PQ, Canada
[8] Ottawa Hosp, Div Infect Dis, Ottawa, ON, Canada
[9] Univ Toronto, Dept Family & Community Med, Toronto, ON M5S 1A1, Canada
[10] Univ Toronto, Dalla Lana Sch Publ Hlth, Toronto, ON M5S 1A1, Canada
[11] Inst Clin Evaluat Sci, Toronto, ON, Canada
来源
BMC MEDICAL RESEARCH METHODOLOGY | 2010年 / 10卷
基金
加拿大健康研究院;
关键词
TIME;
D O I
10.1186/1471-2288-10-51
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: The collection of individual-level pandemic (H1N1) 2009 influenza immunization data was considered important to facilitate optimal vaccine delivery and accurate assessment of vaccine coverage. These data are also critical for research aimed at evaluating the new vaccine's safety and effectiveness. Systems used to collect immunization data include manual approaches in which data are collected and retained on paper, electronic systems in which data are captured on computer at the point of vaccination and hybrid systems which are comprised of both computerized and manual data collection components. This study's objective was to compare the efficiencies and perceptions of data collection methods employed during Canada's pandemic (H1N1) 2009 influenza vaccination campaign. Methods/Design: A pan-Canadian observational study was conducted in a convenience sample of public health clinics and healthcare institutions during the H1N1 vaccination campaign in the fall of 2009. The study design consisted of three stages: Stage 1 involved passive observation of the site's layout, processes and client flow; Stage 2 entailed timing site staff on 20 clients through five core immunization tasks: i) client registration, ii) medical history collection, iii) medical history review, iv) vaccine administration record keeping and v) preparation of proof of vaccine administration for the client; in Stage 3, site staff completed a questionnaire regarding perceived usability of the site's data collection approach. Before the national study began, a pilot study was conducted in three seasonal influenza vaccination sites in Ontario, to both test that the proposed methodology was logistically feasible and to determine inter-rater reliability in the measurements of the research staff. Comparative analyses will be conducted across the range of data collection methods with respect to time required to collect immunization data, number and type of individual-level data elements collected, and clinic staff perceptions of the usability of the method employed at their site, using analysis of variance (ANOVA). Discussion: Various data collection methods were employed at immunization sites across Canada during the pandemic (H1N1) 2009 influenza vaccination campaign. Our comparison of methods can facilitate planning an efficient, coordinated approach for collecting immunization data in future influenza seasons.
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页数:6
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