Kamil Malshy, Stephen Schmit, Borivoj Golijanin, Benjamin Ahn, John Morgan, Amir Farah, Kennon Miller, Dragan Golijanin, Madeline Cancian
{"title":"利用放射组学和营养指标预测富尼耶坏疽患者的长期生存。","authors":"Kamil Malshy, Stephen Schmit, Borivoj Golijanin, Benjamin Ahn, John Morgan, Amir Farah, Kennon Miller, Dragan Golijanin, Madeline Cancian","doi":"10.1177/03915603251318502","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>To evaluate the association of traditional and novel nutritional measurements with survival in Fournier's gangrene (FG) patients.</p><p><strong>Methods: </strong>We reviewed records of FG patients from our tertiary center (Jan 2013-Jan 2022). Radiomic sarcopenia parameters (Psoas Muscle Area [PMA], Roundness, Solidity, and calculated PMA-Index) were measured from admission CT scans at the L3 level using ImageJ software. We assessed sarcopenia's impact on survival through three analyses: Model 1 used a PMI below the sex-adjusted median; Models 2 and 3 used published cutoffs. Kaplan-Meier curves were used to compare survival between sarcopenic and non-sarcopenic patients. Multivariable Cox and logistic regression analyses adjusted for age and the Charlson Comorbidity Index (CCI) to assess mortality risk.</p><p><strong>Results: </strong>Of 130 men and 31 women (82% white), 60 patients (37.3%) had died after a median follow-up of 2.2 years (IQR 0.9-4.4). Survival rates were 94% at 30 days, 92% at 90 days, 80% at 1 year, 77% at 2 years, and 56% at 5 years. Non-survivors were older (median age 63 vs 55.1 years, <i>p</i> < 0.001) and had higher median CCI (4.8 vs 3; <i>p</i> < 0.001).In Model 1, sarcopenic patients had a non-significant increased mortality risk with hazard ratio (HR 1.47, 95% CI 0.82-2.64, <i>p</i> = 0.196). Models 2 and 3 showed similar results (HR 1.41, 95% CI 0.70-2.84, <i>p</i> = 0.325; HR 1.35, 95% CI 0.70-2.61, <i>p</i> = 0.364). None of the models were significant when adjusting for CCI and age. Survivors had better traditional metabolic profiles, including higher albumin (3.1vs 2.7 g/dL), hemoglobin (12.4vs 11.4 g/dL), and lower creatinine (1.39 vs 2.1 mg/dL); however, none of these were significant when adjusting for age and CCI.</p><p><strong>Conclusions: </strong>Despite a mild trend, none of the sarcopenia models were able to predict long-term mortality in FG patients in our cohort. This well-known, cost-effective nutritional predictor still requires further research to optimize its utilization in the FG patient population.</p>","PeriodicalId":23574,"journal":{"name":"Urologia Journal","volume":" ","pages":"3915603251318502"},"PeriodicalIF":0.8000,"publicationDate":"2025-02-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Harnessing radiomics and nutritional metrics to predict long-term survival in Fournier's gangrene patients.\",\"authors\":\"Kamil Malshy, Stephen Schmit, Borivoj Golijanin, Benjamin Ahn, John Morgan, Amir Farah, Kennon Miller, Dragan Golijanin, Madeline Cancian\",\"doi\":\"10.1177/03915603251318502\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Purpose: </strong>To evaluate the association of traditional and novel nutritional measurements with survival in Fournier's gangrene (FG) patients.</p><p><strong>Methods: </strong>We reviewed records of FG patients from our tertiary center (Jan 2013-Jan 2022). Radiomic sarcopenia parameters (Psoas Muscle Area [PMA], Roundness, Solidity, and calculated PMA-Index) were measured from admission CT scans at the L3 level using ImageJ software. We assessed sarcopenia's impact on survival through three analyses: Model 1 used a PMI below the sex-adjusted median; Models 2 and 3 used published cutoffs. Kaplan-Meier curves were used to compare survival between sarcopenic and non-sarcopenic patients. Multivariable Cox and logistic regression analyses adjusted for age and the Charlson Comorbidity Index (CCI) to assess mortality risk.</p><p><strong>Results: </strong>Of 130 men and 31 women (82% white), 60 patients (37.3%) had died after a median follow-up of 2.2 years (IQR 0.9-4.4). Survival rates were 94% at 30 days, 92% at 90 days, 80% at 1 year, 77% at 2 years, and 56% at 5 years. Non-survivors were older (median age 63 vs 55.1 years, <i>p</i> < 0.001) and had higher median CCI (4.8 vs 3; <i>p</i> < 0.001).In Model 1, sarcopenic patients had a non-significant increased mortality risk with hazard ratio (HR 1.47, 95% CI 0.82-2.64, <i>p</i> = 0.196). Models 2 and 3 showed similar results (HR 1.41, 95% CI 0.70-2.84, <i>p</i> = 0.325; HR 1.35, 95% CI 0.70-2.61, <i>p</i> = 0.364). None of the models were significant when adjusting for CCI and age. Survivors had better traditional metabolic profiles, including higher albumin (3.1vs 2.7 g/dL), hemoglobin (12.4vs 11.4 g/dL), and lower creatinine (1.39 vs 2.1 mg/dL); however, none of these were significant when adjusting for age and CCI.</p><p><strong>Conclusions: </strong>Despite a mild trend, none of the sarcopenia models were able to predict long-term mortality in FG patients in our cohort. This well-known, cost-effective nutritional predictor still requires further research to optimize its utilization in the FG patient population.</p>\",\"PeriodicalId\":23574,\"journal\":{\"name\":\"Urologia Journal\",\"volume\":\" \",\"pages\":\"3915603251318502\"},\"PeriodicalIF\":0.8000,\"publicationDate\":\"2025-02-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Urologia Journal\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1177/03915603251318502\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"UROLOGY & NEPHROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Urologia Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1177/03915603251318502","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"UROLOGY & NEPHROLOGY","Score":null,"Total":0}
引用次数: 0
摘要
目的:评价富尼耶坏疽(FG)患者传统和新型营养测量方法与生存的关系。方法:回顾我院三级中心(2013年1月- 2022年1月)FG患者的记录。使用ImageJ软件从入院CT扫描的L3层测量放射学肌肉减少症参数(腰肌面积[PMA],圆度,实心度和计算的PMA指数)。我们通过三个分析评估了肌肉减少症对生存的影响:模型1使用低于性别调整中位数的PMI;模型2和模型3采用公布截止值。Kaplan-Meier曲线用于比较肌肉减少症和非肌肉减少症患者的生存率。多变量Cox和logistic回归分析调整了年龄和Charlson合并症指数(CCI)来评估死亡风险。结果:在130名男性和31名女性(82%为白人)中,60名患者(37.3%)在中位随访2.2年(IQR 0.9-4.4)后死亡。30天生存率为94%,90天生存率为92%,1年生存率为80%,2年生存率为77%,5年生存率为56%。非幸存者年龄较大(中位年龄63 vs 55.1岁,p p p = 0.196)。模型2和模型3结果相似(HR 1.41, 95% CI 0.70-2.84, p = 0.325;HR 1.35, 95% CI 0.70-2.61, p = 0.364)。当调整CCI和年龄时,没有一个模型是显著的。幸存者具有更好的传统代谢谱,包括较高的白蛋白(3.1vs 2.7 g/dL)、血红蛋白(12.4vs 11.4 g/dL)和较低的肌酐(1.39 vs 2.1 mg/dL);然而,当调整年龄和CCI时,这些都不显著。结论:尽管有轻微的趋势,但在我们的队列中,没有一个肌少症模型能够预测FG患者的长期死亡率。这一众所周知的、具有成本效益的营养预测指标仍需要进一步研究,以优化其在FG患者群体中的应用。
Harnessing radiomics and nutritional metrics to predict long-term survival in Fournier's gangrene patients.
Purpose: To evaluate the association of traditional and novel nutritional measurements with survival in Fournier's gangrene (FG) patients.
Methods: We reviewed records of FG patients from our tertiary center (Jan 2013-Jan 2022). Radiomic sarcopenia parameters (Psoas Muscle Area [PMA], Roundness, Solidity, and calculated PMA-Index) were measured from admission CT scans at the L3 level using ImageJ software. We assessed sarcopenia's impact on survival through three analyses: Model 1 used a PMI below the sex-adjusted median; Models 2 and 3 used published cutoffs. Kaplan-Meier curves were used to compare survival between sarcopenic and non-sarcopenic patients. Multivariable Cox and logistic regression analyses adjusted for age and the Charlson Comorbidity Index (CCI) to assess mortality risk.
Results: Of 130 men and 31 women (82% white), 60 patients (37.3%) had died after a median follow-up of 2.2 years (IQR 0.9-4.4). Survival rates were 94% at 30 days, 92% at 90 days, 80% at 1 year, 77% at 2 years, and 56% at 5 years. Non-survivors were older (median age 63 vs 55.1 years, p < 0.001) and had higher median CCI (4.8 vs 3; p < 0.001).In Model 1, sarcopenic patients had a non-significant increased mortality risk with hazard ratio (HR 1.47, 95% CI 0.82-2.64, p = 0.196). Models 2 and 3 showed similar results (HR 1.41, 95% CI 0.70-2.84, p = 0.325; HR 1.35, 95% CI 0.70-2.61, p = 0.364). None of the models were significant when adjusting for CCI and age. Survivors had better traditional metabolic profiles, including higher albumin (3.1vs 2.7 g/dL), hemoglobin (12.4vs 11.4 g/dL), and lower creatinine (1.39 vs 2.1 mg/dL); however, none of these were significant when adjusting for age and CCI.
Conclusions: Despite a mild trend, none of the sarcopenia models were able to predict long-term mortality in FG patients in our cohort. This well-known, cost-effective nutritional predictor still requires further research to optimize its utilization in the FG patient population.