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Predictive value of 5-Factor modified frailty index in Oncologic and benign hysterectomies

BACKGROUND: The 5-factor modified frailty index (mFI-5) has been validated against the original 11-factor modified frailty index in gynecologic surgery, however its utility has not been evaluated between benign versus gynecologic oncology patient populations. OBJECTIVE: To evaluate the predictive va...

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Autores principales: Hermann, Catherine E., Koelper, Nathanael C., Andriani, Leslie, Latif, Nawar A., Ko, Emily M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9424918/
https://www.ncbi.nlm.nih.gov/pubmed/36051500
http://dx.doi.org/10.1016/j.gore.2022.101063
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author Hermann, Catherine E.
Koelper, Nathanael C.
Andriani, Leslie
Latif, Nawar A.
Ko, Emily M.
author_facet Hermann, Catherine E.
Koelper, Nathanael C.
Andriani, Leslie
Latif, Nawar A.
Ko, Emily M.
author_sort Hermann, Catherine E.
collection PubMed
description BACKGROUND: The 5-factor modified frailty index (mFI-5) has been validated against the original 11-factor modified frailty index in gynecologic surgery, however its utility has not been evaluated between benign versus gynecologic oncology patient populations. OBJECTIVE: To evaluate the predictive value of the mFI-5 in identifying women at increased risk for major postoperative complications, readmission, or death within 30 days of hysterectomy for benign and oncologic indications. METHODS: Patients who underwent hysterectomy between 2015 and 2017 were identified from the NSQIP database and stratified into benign or malignant indications. Demographic and mFI-5 variables were extracted. The mFI-5 was calculated by dividing the sum of all affirmative variables by the total number of input variables in the database. Logistic regression modeling was performed adjusting for confounders. C-statistic with 95% CI was obtained post-regression. RESULTS: 80,293 hysterectomies (59,078 benign and 21,215 oncologic) were identified. The benign group was more likely to have an mFI-5 score of 0 (70 % vs 50 %, p = 0.001) and had shorter operative times (p = 0.001). In the benign group, mFI-5 was a strong predictor of mortality (c = 0.819, CI 0.704–0.933). Within the oncology group, the mFI-5 was a strong predictor of mortality (c = 0.801, CI 0.750–0.851), particularly for uterine and cervical cancers. It was moderately predictive of readmission (c = 0.671, CI 0.656–0.686) and strongly predictive of Clavien-Dindo class III and IV complications (c = 0.732, CI 0.713–0.750). CONCLUSION: The mFI-5 is a strong predictor of 30-day mortality and serious postoperative complications. These findings have the potential to improve identification of high-risk patients in the preoperative setting.
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spelling pubmed-94249182022-08-31 Predictive value of 5-Factor modified frailty index in Oncologic and benign hysterectomies Hermann, Catherine E. Koelper, Nathanael C. Andriani, Leslie Latif, Nawar A. Ko, Emily M. Gynecol Oncol Rep Research Report BACKGROUND: The 5-factor modified frailty index (mFI-5) has been validated against the original 11-factor modified frailty index in gynecologic surgery, however its utility has not been evaluated between benign versus gynecologic oncology patient populations. OBJECTIVE: To evaluate the predictive value of the mFI-5 in identifying women at increased risk for major postoperative complications, readmission, or death within 30 days of hysterectomy for benign and oncologic indications. METHODS: Patients who underwent hysterectomy between 2015 and 2017 were identified from the NSQIP database and stratified into benign or malignant indications. Demographic and mFI-5 variables were extracted. The mFI-5 was calculated by dividing the sum of all affirmative variables by the total number of input variables in the database. Logistic regression modeling was performed adjusting for confounders. C-statistic with 95% CI was obtained post-regression. RESULTS: 80,293 hysterectomies (59,078 benign and 21,215 oncologic) were identified. The benign group was more likely to have an mFI-5 score of 0 (70 % vs 50 %, p = 0.001) and had shorter operative times (p = 0.001). In the benign group, mFI-5 was a strong predictor of mortality (c = 0.819, CI 0.704–0.933). Within the oncology group, the mFI-5 was a strong predictor of mortality (c = 0.801, CI 0.750–0.851), particularly for uterine and cervical cancers. It was moderately predictive of readmission (c = 0.671, CI 0.656–0.686) and strongly predictive of Clavien-Dindo class III and IV complications (c = 0.732, CI 0.713–0.750). CONCLUSION: The mFI-5 is a strong predictor of 30-day mortality and serious postoperative complications. These findings have the potential to improve identification of high-risk patients in the preoperative setting. Elsevier 2022-08-23 /pmc/articles/PMC9424918/ /pubmed/36051500 http://dx.doi.org/10.1016/j.gore.2022.101063 Text en © 2022 The Authors. Published by Elsevier Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Report
Hermann, Catherine E.
Koelper, Nathanael C.
Andriani, Leslie
Latif, Nawar A.
Ko, Emily M.
Predictive value of 5-Factor modified frailty index in Oncologic and benign hysterectomies
title Predictive value of 5-Factor modified frailty index in Oncologic and benign hysterectomies
title_full Predictive value of 5-Factor modified frailty index in Oncologic and benign hysterectomies
title_fullStr Predictive value of 5-Factor modified frailty index in Oncologic and benign hysterectomies
title_full_unstemmed Predictive value of 5-Factor modified frailty index in Oncologic and benign hysterectomies
title_short Predictive value of 5-Factor modified frailty index in Oncologic and benign hysterectomies
title_sort predictive value of 5-factor modified frailty index in oncologic and benign hysterectomies
topic Research Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9424918/
https://www.ncbi.nlm.nih.gov/pubmed/36051500
http://dx.doi.org/10.1016/j.gore.2022.101063
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