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常规采集的患者报告结局数据是否代表择期冠状动脉血运重建患者的实际病例组合?

Does routinely collected patient-reported outcome data represent the actual case-mix of elective coronary revascularization patients?

机构信息

School of Pharmacy, University of Eastern Finland, Yliopistonranta 1, FI-70210, Kuopio, Finland.

Kuopio University Hospital, Heart Center and Research Centre for Comparative Effectiveness and Patient Safety (RECEPS), Yliopistonranta 1, FI-70210, Kuopio, Finland.

出版信息

Eur Heart J Qual Care Clin Outcomes. 2018 Apr 1;4(2):113-119. doi: 10.1093/ehjqcco/qcx038.

Abstract

AIMS

Patient-reported outcomes (PROs) are valuable for effectiveness evaluation, but it is unknown whether the patient views obtained represent the actual case mix. We studied the representativeness of the responses obtained to a routinely administered health-related quality of life (HRQoL) questionnaire in a cardiology unit.

METHODS AND RESULTS

Elective coronary artery bypass grafting (CABG; n = 404) and percutaneous coronary intervention (PCI; n = 738) patients operated during June 2012 to August 2014 in the Heart Center, Kuopio University Hospital. The characteristics of the patients with a baseline (n = 260 and 290 for CABG and PCI, respectively) or both baseline and follow-up HRQoL measurements (n = 203 and 189 for CABG and PCI, respectively) were compared with those who did not respond (n = 144 and 448 for CABG and PCI). Baseline questionnaires were less likely obtained from older CABG patients (odds ratio 0.51, 95% confidence interval 0.28-0.91) and those with more severe disease (0.20, 0.05-0.79). Among PCI patients, women (0.64, 0.45-0.91), smokers (0.74, 0.53-1.04), and those with more severe disease (0.26, 0.13-0.52) or more hospital days were underrepresented.

CONCLUSION

Routinely collected PROs in cardiac patients may be biased towards younger and healthier patients. This needs to be recognized when evaluating the representativeness of such data. The routine collection of these data should be adequately resourced.

摘要

目的

患者报告的结局(PROs)对于评估有效性很有价值,但尚不清楚获得的患者观点是否代表实际病例组合。我们研究了在心脏病学单元常规管理的健康相关生活质量(HRQoL)问卷中获得的反应的代表性。

方法和结果

2012 年 6 月至 2014 年 8 月期间,在库奥皮奥大学医院心脏中心接受选择性冠状动脉旁路移植术(CABG;n=404)和经皮冠状动脉介入治疗(PCI;n=738)的患者。基线时(CABG 和 PCI 分别为 n=260 和 290)和基线及随访 HRQoL 测量时(CABG 和 PCI 分别为 n=203 和 189)有特征的患者与未应答的患者(CABG 和 PCI 分别为 n=144 和 448)进行了比较。基线问卷不太可能从较年长的 CABG 患者(优势比 0.51,95%置信区间 0.28-0.91)和疾病更严重的患者(0.20,0.05-0.79)中获得。在 PCI 患者中,女性(0.64,0.45-0.91)、吸烟者(0.74,0.53-1.04)、疾病更严重(0.26,0.13-0.52)或住院天数更多的患者代表性不足。

结论

在心脏患者中常规收集的 PROs 可能偏向于更年轻和更健康的患者。在评估此类数据的代表性时,需要认识到这一点。应充分为这些数据的常规收集提供资源。

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