首页> 外文期刊>The Journal of Urology >Improved prediction of long-term, other cause mortality in men with prostate cancer.
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Improved prediction of long-term, other cause mortality in men with prostate cancer.

机译:改善前列腺癌男性长期,其他原因死亡率的预测。

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PURPOSE: Comorbidity assessment is essential to triage of care for men with prostate cancer. We identified long-term risks of other cause mortality associated with comorbidities in the Charlson index and applied these to the creation of a prostate cancer specific comorbidity index. MATERIALS AND METHODS: We sampled 1,598 cases of prostate cancer diagnosed in 1997 to 2004 at the Greater Los Angeles and Long Beach Veterans Affairs Medical Centers. We used Cox proportional hazards modeling to determine the risks of other cause mortality associated with comorbidities and used these hazard ratios to re-weight the Charlson index. We then compared the ability of each index to predict other cause mortality. RESULTS: Cox modeling showed that moderate to severe liver disease, metastatic solid tumor, lymphoma and leukemia carried the highest risk (HR greater than 5) for other cause mortality, followed by moderate to severe chronic obstructive pulmonary disease, moderate to severe renal disease, dementia, hemiplegia and congestive heart failure (HR 2.5 to less than 3.5). The revised and original Charlson indices performed similarly in predicting other cause mortality across all patients (c-index 0.816 vs 0.802). However, in survival analysis our revised index identified 137 men with a greater than 90% probability of other cause mortality within 10 years while the original Charlson identified only 51. In multivariate modeling the odds of 5-year other cause mortality for men with original Charlson scores 1, 2, 3 and 4+ were 2.9, 6.0, 9.2 and 29.8, respectively, compared with 3.9, 6.2, 12.8 and 84.2 for the revised index. CONCLUSIONS: Re-weighting the Charlson index allowed for more accurate identification of men at highest risk for other cause mortality. Our revised index may be used to aid medical decision making for men with prostate cancer.
机译:目的:合并症评估对于前列腺癌男性的分诊至关重要。我们在查尔森指数中确定了与合并症相关的其他原因致死的长期风险,并将其应用于创建前列腺癌特定合并症指数。材料与方法:我们从1997年至2004年在大洛杉矶和长滩退伍军人事务医疗中心诊断出的1,598例前列腺癌病例中进行了抽样。我们使用Cox比例风险模型来确定与合并症相关的其他原因致死的风险,并使用这些风险比率重新加权Charlson指数。然后,我们比较了每个指标预测其他原因死亡率的能力。结果:Cox模型显示,中重度肝病,转移性实体瘤,淋巴瘤和白血病的其他原因致死风险最高(HR大于5),其次是中重度慢性阻塞性肺疾病,中重度肾病,痴呆,偏瘫和充血性心力衰竭(HR 2.5至小于3.5)。修订后的和最初的Charlson指数在预测所有患者的其他原因死亡率方面表现相似(c指数0.816 vs 0.802)。但是,在生存分析中,我们修订后的指数确定了137名男性在10年内有其他原因致死的可能性高于90%,而原始查尔森只鉴定出51名。在多变量建模中,具有原始查尔森的男性5年内其他致死率的可能性1、2、3和4+得分分别为2.9、6.0、9.2和29.8,而经修订的指数分别为3.9、6.2、12.8和84.2。结论:重新对Charlson指数进行加权可以更准确地识别其他原因致死风险最高的男性。我们修订后的指数可用于协助前列腺癌男性的医疗决策。

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