Thoracic Service, Department of Surgery, Memorial Sloan-Kettering Cancer Center, New York, New York 10021, USA.
Ann Thorac Surg. 2012 Sep;94(3):881-7; discussion 887-8. doi: 10.1016/j.athoracsur.2012.04.082. Epub 2012 Jun 27.
The National Quality Forum endorses prolonged length of stay of more than 14 days (PLOS) as a quality metric for lobectomy for lung cancer. Because PLOS rates are lower than complication rates, we hypothesized that PLOS misses a significant proportion of clinically important events.
A retrospective study was performed on patients undergoing lobectomy (2000 to 2009). The severity of adverse events was based on the National Cancer Institute common terminology criteria for adverse events (grade 2 or higher indicates symptoms or need for medical intervention; grade 5 indicates death).
Among 2,667 patients, 163 (6%) experienced PLOS and 773 (29%) experienced an adverse event. Although the frequency of adverse events was higher among the PLOS group (99% [161 of 163] versus 24% [612 of 2504]), 79% (612 of 773) of adverse events occurred in the non-PLOS group. Whereas PLOS was associated with more severe events, 89% of those in the non-PLOS group experienced a grade 2 or higher event. Likewise, although PLOS was associated with the lowest 5-year survival rate (31%), patients in the non-PLOS group who had an adverse event had significantly lower survival rates than patients in the non-PLOS group who did not have any adverse events (55% versus 68%, p<0.001; adjusted hazard ratio 1.3 [95% confidence interval: 1.1 to 1.6]).
The PLOS missed a high proportion of adverse events defined by the need for ongoing inpatient therapy and an association with poor long-term survival. These findings have implications for efficient and fair performance assessment in the setting of a quality improvement program.
国家质量论坛认可超过 14 天的住院时间延长(PLOS)作为肺癌肺叶切除术的质量指标。由于 PLOS 发生率低于并发症发生率,我们假设 PLOS 错过了相当一部分临床上重要的事件。
对 2000 年至 2009 年间接受肺叶切除术的患者进行了回顾性研究。不良事件的严重程度基于国家癌症研究所不良事件通用术语标准(2 级或更高表示症状或需要医疗干预;5 级表示死亡)。
在 2667 名患者中,有 163 名(6%)经历了 PLOS,773 名(29%)发生了不良事件。尽管 PLOS 组的不良事件发生率更高(99%[161/163]比 24%[612/2504]),但 79%(612/773)的不良事件发生在非 PLOS 组。虽然 PLOS 与更严重的事件相关,但非 PLOS 组中有 89%的患者发生了 2 级或更高级别的事件。同样,尽管 PLOS 与最低的 5 年生存率(31%)相关,但在非 PLOS 组中发生不良事件的患者的生存率明显低于在非 PLOS 组中未发生任何不良事件的患者(55%比 68%,p<0.001;调整后的危险比 1.3[95%置信区间:1.1 至 1.6])。
PLOS 错过了相当一部分需要持续住院治疗和与不良长期生存相关的不良事件。这些发现对质量改进计划背景下的高效和公平绩效评估具有影响。