癌症医用大麻登记使用者调查的数据质量:无响应和测量误差。

Jeanette Y Ziegenfuss, Helen M Parsons, Anne H Blaes, Bruce Lindgren, Julia Andersen, Susan Park, Patricia I Jewett, Arjun Gupta, Dylan M Zylla
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引用次数: 0

摘要

了解癌症患者吸食大麻的最佳方式是通过调查自我报告。由于大麻在联邦法律上仍然是非法的,因此调查可能会受到无响应和测量问题的影响,从而影响数据质量。我们对明尼苏达医用大麻计划 (MCP) 中因癌症相关疾病而使用医用大麻的个人进行了调查。虽然调查对象年龄较大,但在种族和民族、性别或大麻注册费减免情况方面并无差异。与未回复者相比,回复者购买大麻的时间更近,完成独立症状评估的时间也更近,这表明存在一定的非回复误差。在应答者中,关于年龄、种族、性别、登记认证和大麻购买历史的自我报告数据与 MCP 管理数据相似。根据登记处的低收入登记资格,应答者报告接受医疗补助的可能性低于预期。虽然应注意可能出现的非响应误差,但调查是确定该人群大麻行为模式的可靠工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Data quality in a survey of registered medical cannabis users with cancer: nonresponse and measurement error.

Cannabis use among individuals with cancer is best understood using survey self-report. As cannabis remains federally illegal, surveys could be subject to nonresponse and measurement issues impacting data quality. We surveyed individuals using medical cannabis for a cancer-related condition in the Minnesota Medical Cannabis Program (MCP). Although survey responders are older, there are no differences by race and ethnicity, gender, or receipt of reduced cannabis registry enrollment fee. Responders made a more recent purchase and more recently completed an independent symptom assessment for the registry than nonresponders, suggesting some opportunity for nonresponse error. Among responders, self-report and MCP administrative data with respect to age, race, gender, registry certification, and cannabis purchase history were similar. Responders were less likely to report receipt of Medicaid than would be expected based on registry low-income enrollment eligibility. Although attention should be paid to potential for nonresponse error, surveys are a reliable tool to ascertain cannabis behavior patterns in this population.

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CiteScore
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