Association between chronic pain and attrition: a prospective analysis of a national sample of midlife adults in the USA, 2004–2014

Yunlong Liang
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Abstract

Health conditions of participants can significantly affect longitudinal drop-out in population-based epidemiological surveys, yet few studies have examined the association between chronic pain (CP) and follow-up attrition.The Midlife in the United States study (MIDUS) was used to explore the longitudinal association between CP and survey attrition. CP was assessed by three measures: the presence of CP, CP interference and the number of pain sites at MIDUS 2. The types of sample attrition at MIDUS 3 encompassed several categories: complete, refusal to participate, inability to participate due to physical or mental constraints, deceased, non-working numbers, participants consistently unavailable for interviews, global refusal or withdrew from the study and not fielded. Multinomial logistic regression was employed to examine these relationships and to explore the moderation effects of sociodemographic variables and multiple chronic conditions on these associations.High-interference pain was associated with a 162% increased risk (RR 2.62, 95% CI 1.12 to 6.16, p=0.026) of being physically and mentally unable to participate in MIDUS 3. Individuals reporting the presence of CP (RR 0.65, 95% CI 0.45 to 0.95, p=0.028) and those with three or more CP sites (RR 0.48, 95% CI 0.27 to 0.87, p=0.016) were less likely to refuse participation in MIDUS 3. However, no further significant associations or moderating effects were identified.Population-based epidemiological surveys may be susceptible to attrition bias from participants with CP, necessitating the adoption of adaptive survey methodologies.
慢性疼痛与自然减员之间的关系:对 2004-2014 年美国全国中年人样本的前瞻性分析
参与者的健康状况会对基于人口的流行病学调查中的纵向退出产生重大影响,但很少有研究探讨了慢性疼痛(CP)与随访流失之间的关联。慢性疼痛通过三种测量方法进行评估:慢性疼痛的存在、慢性疼痛的干扰以及在 MIDUS 2 时疼痛部位的数量。MIDUS 3 的样本损耗类型包括几类:完全损耗、拒绝参与、因身体或精神限制无法参与、死亡、非工作号码、参与者始终无法接受访谈、全面拒绝或退出研究以及未进行实地调查。高干扰性疼痛与身心无法参与 MIDUS 3 的风险增加 162% 相关(RR 2.62,95% CI 1.12 至 6.16,p=0.026)。65, 95% CI 0.45 to 0.95, p=0.028)和有三个或三个以上 CP 病变部位(RR 0.48, 95% CI 0.27 to 0.87, p=0.016)的人拒绝参与 MIDUS 3 的可能性较低,但未发现进一步的显著关联或调节效应。
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