Patel Roma, Biros Michelle H, Moore Johanna, Miner James R
Department of Emergency Medicine, Hennepin County Medical Center, Minneapolis, MN.
Acad Emerg Med. 2014 Dec;21(12):1478-84. doi: 10.1111/acem.12543.
The primary objective of this study was to determine whether patient-described pain correlates with patient-described stress, anxiety, and satisfaction with ongoing treatment and if that correlation differs by gender.
This was a prospective observational study at an urban, Level I trauma center conducted between June 1, 2010, and January 1, 2013. Patients reporting pain rated greater than 3 of 10 were eligible. Patients who qualified and consented for participation completed demographic and pain, anxiety, stress, and satisfaction scales at baseline, every 30 minutes, and at discharge. Data were analyzed using analysis of variance, chi-square tests, t-tests, multiple regression, and the Wilcoxon-Mann-Whitney rank test.
A total of 7,124 patients were screened for enrollment. Of those, 3,495 (49%) did not qualify at screening for various reasons, including insufficient pain levels (17.5%), elected not to participate (37.7%), did not qualify for other reasons (12.4%), and reason not captured (32.4%). A total of 3,629 (51%) screened patients were eligible and consented. Of those, 620 (16.8%) did not have any data collected past baseline, leaving 3,009 as the final sample size. The patients completing data collection had a median age of 39 years (range = 18 to 90 years), and 50% were male. The mean presenting pain visual analog scale (VAS) score was 71.5 mm. Presenting stress and anxiety VAS scores were significantly higher in females (0.61 and 0.53, respectively) than males (0.56 and 0.50, respectively), whereas presenting pain VAS (0.71 male and 0.72 female) and satisfaction VAS (0.34 male and 0.35 female) did not differ by sex. Ethnicity, education, and income were all statistically different when compared with baseline pain, stress, anxiety, and satisfaction. Male gender was associated with a significant change in pain over time from baseline (coefficient = 0.040, p = 0.037); however, when adjusting for age, ethnicity, education, and income, and for changes in stress, anxiety, and satisfaction VAS scores, changes in pain related to male gender was no longer significant (coefficient = 0.034, p = 0.11). When asked about their satisfaction with the results of the pain treatment that had been provided, patients reported a median of 2 (out of 6, 1 = satisfied, 6 = dissatisfied; interquartile range = 1 to 2). There was no significant difference between sexes (p > 0.90).
Patient-reported stress and anxiety were higher among female patients than male patients, but there was no significant difference in reported pain and satisfaction between sexes. Sex alone was not a significant predictor of change in pain for patients presenting to the emergency department with pain-related complaints. Anxiety and stress may potentially influence the pain-gender relationship.
本研究的主要目的是确定患者自述的疼痛是否与患者自述的压力、焦虑以及对正在进行的治疗的满意度相关,以及这种相关性是否因性别而异。
这是一项在城市一级创伤中心进行的前瞻性观察性研究,研究时间为2010年6月1日至2013年1月1日。报告疼痛评分大于10分制中的3分的患者符合条件。符合条件并同意参与的患者在基线、每30分钟以及出院时完成人口统计学和疼痛、焦虑、压力及满意度量表的填写。数据采用方差分析、卡方检验、t检验、多元回归以及Wilcoxon-Mann-Whitney秩和检验进行分析。
共有7124名患者被筛选纳入研究。其中,3495名(49%)因各种原因在筛选时不符合条件,包括疼痛程度不足(17.5%)、选择不参与(37.7%)、因其他原因不符合条件(12.4%)以及原因未记录(32.4%)。共有3629名(51%)筛选合格的患者同意参与。其中,620名(16.8%)在基线后未收集到任何数据,最终样本量为3009名。完成数据收集的患者中位年龄为39岁(范围 = 18至90岁),50%为男性。疼痛视觉模拟量表(VAS)的平均初始评分是71.5毫米。女性的初始压力和焦虑VAS评分(分别为0.61和0.53)显著高于男性(分别为0.56和0.50),而初始疼痛VAS评分(男性0.71,女性0.72)和满意度VAS评分(男性0.34,女性0.35)在性别上没有差异。与基线时的疼痛、压力、焦虑和满意度相比,种族、教育程度和收入在统计学上均存在差异。男性性别与从基线开始随时间的疼痛显著变化相关(系数 = 0.040,p = 0.037);然而,在调整年龄、种族、教育程度和收入以及压力、焦虑和满意度VAS评分的变化后,与男性性别相关的疼痛变化不再显著(系数 = 0.034,p = 0.11)。当被问及对所提供疼痛治疗结果的满意度时,患者报告的中位数为2(满分6分,1 = 满意,6 = 不满意;四分位间距 = 1至2)。性别之间没有显著差异(p > 0.90)。
女性患者自述的压力和焦虑高于男性患者,但报告的疼痛和满意度在性别上没有显著差异。对于因疼痛相关主诉前往急诊科就诊的患者,仅性别不是疼痛变化的显著预测因素。焦虑和压力可能会潜在地影响疼痛与性别的关系。