Factors Associated with 1-Year Mortality in Elderly Patients (Age ≥ 80 Years) with Cancer Undergoing Major Abdominal Surgery: A Retrospective Cohort Study.


Journal

Annals of surgical oncology
ISSN: 1534-4681
Titre abrégé: Ann Surg Oncol
Pays: United States
ID NLM: 9420840

Informations de publication

Date de publication:
Dec 2023
Historique:
received: 23 05 2023
accepted: 13 09 2023
medline: 8 11 2023
pubmed: 10 10 2023
entrez: 9 10 2023
Statut: ppublish

Résumé

The number of elderly patients undergoing major abdominal surgery is increasing, but the factors affecting their postoperative outcomes remain unclear. This study aimed to identify the factors associated with 1-year mortality among elderly patients (age ≥ 80 years) with cancer undergoing major abdominal surgery. This retrospective cohort study was conducted from March 2009 to December 2020. The study enrolled 378 patients 80 years old or older who underwent major abdominal surgery. The main outcome was 1-year mortality, and the factors associated with mortality were analyzed. Of the 378 patients, 92 died at 1 year (24.3%), whereas the 30-day mortality rate was 4% (n = 15). In the multivariate analysis, the factors independently associated with 1-year mortality were preoperative Eastern Cooperative Oncology Group (ECOG) performance status (PS) score higher than 1 (odds ratio [OR], 3.189; 95% confidence interval [CI], 1.595-6.377; p = 0.001), preoperative weight loss greater than 3 kg (OR, 2.145; 95% CI, 1.044-4.404; p = 0.038), use of an intraoperative vasopressor (OR, 3.090; 95% CI, 1.188-8.042; p = 0.021), and postoperative red blood cell units (OR, 1.212; 95% CI, 1.045-1.405; p = 0.011). Survival was associated with perioperative management according to an enhanced recovery after surgery (ERAS) protocol (OR, 0.370; 95% CI, 0.160-0.854; p = 0.006) and supramesocolic surgery (OR, 0.371; 95% CI, 0.158-0.871; p = 0.023). The study identified several factors associated with an encouraging 1-year mortality rate in this setting. These results highlight the need for identification of suitable targets to optimize pre-, intra-, and postoperative management in order to improve outcomes for this vulnerable population.

Sections du résumé

BACKGROUND BACKGROUND
The number of elderly patients undergoing major abdominal surgery is increasing, but the factors affecting their postoperative outcomes remain unclear. This study aimed to identify the factors associated with 1-year mortality among elderly patients (age ≥ 80 years) with cancer undergoing major abdominal surgery.
METHODS METHODS
This retrospective cohort study was conducted from March 2009 to December 2020. The study enrolled 378 patients 80 years old or older who underwent major abdominal surgery. The main outcome was 1-year mortality, and the factors associated with mortality were analyzed.
RESULTS RESULTS
Of the 378 patients, 92 died at 1 year (24.3%), whereas the 30-day mortality rate was 4% (n = 15). In the multivariate analysis, the factors independently associated with 1-year mortality were preoperative Eastern Cooperative Oncology Group (ECOG) performance status (PS) score higher than 1 (odds ratio [OR], 3.189; 95% confidence interval [CI], 1.595-6.377; p = 0.001), preoperative weight loss greater than 3 kg (OR, 2.145; 95% CI, 1.044-4.404; p = 0.038), use of an intraoperative vasopressor (OR, 3.090; 95% CI, 1.188-8.042; p = 0.021), and postoperative red blood cell units (OR, 1.212; 95% CI, 1.045-1.405; p = 0.011). Survival was associated with perioperative management according to an enhanced recovery after surgery (ERAS) protocol (OR, 0.370; 95% CI, 0.160-0.854; p = 0.006) and supramesocolic surgery (OR, 0.371; 95% CI, 0.158-0.871; p = 0.023).
CONCLUSION CONCLUSIONS
The study identified several factors associated with an encouraging 1-year mortality rate in this setting. These results highlight the need for identification of suitable targets to optimize pre-, intra-, and postoperative management in order to improve outcomes for this vulnerable population.

Identifiants

pubmed: 37814178
doi: 10.1245/s10434-023-14365-8
pii: 10.1245/s10434-023-14365-8
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

8083-8093

Informations de copyright

© 2023. Society of Surgical Oncology.

Références

Pilleron S, Soto-Perez-de-Celis E, Vignat J, et al. Estimated global cancer incidence in the oldest adults in 2018 and projections to 2050. Int J Cancer. 2021;148:601–8.
doi: 10.1002/ijc.33232 pubmed: 32706917
World Health Organization. World report on ageing and health. Geneva, Switzerland: World Health Organization; 2015.
Arnold M, Rutherford MJ, Bardot A, et al. Progress in cancer survival, mortality, and incidence in seven high-income countries 1995–2014 (ICBP SURVMARK-2): a population-based study. Lancet Oncol. 2019;20:1493–505.
doi: 10.1016/S1470-2045(19)30456-5 pubmed: 31521509 pmcid: 6838671
Colonna M, Bossard N, Remontet L, et al. Changes in the risk of death from cancer up to five years after diagnosis in elderly patients: a study of five common cancers. Int J Cancer. 2010;127:924–31.
doi: 10.1002/ijc.25101 pubmed: 19998335
Gouverneur A, Salvo F, Berdaï D, et al. Inclusion of elderly or frail patients in randomized controlled trials of targeted therapies for the treatment of metastatic colorectal cancer: a systematic review. J Geriatric Oncol. 2018;9:15–23.
doi: 10.1016/j.jgo.2017.08.001
Lin H-S, Watts JN, Peel NM, et al. Frailty and postoperative outcomes in older surgical patients: a systematic review. BMC Geriatrics. 2016;16:157.
doi: 10.1186/s12877-016-0329-8 pubmed: 27580947 pmcid: 5007853
Lopez-Lopez V, Gómez-Ruiz AJ, Eshmuminov D, et al. Surgical oncology in patients aged 80 years and older is associated with increased postoperative morbidity and mortality: a systematic review and meta-analysis of literature over 25 years. Surg Oncol. 2020;33:81–95.
doi: 10.1016/j.suronc.2019.12.007 pubmed: 32561103
Nepogodiev D, Martin J, Biccard B, et al. Global burden of postoperative death. Lancet. 2019;393:401.
doi: 10.1016/S0140-6736(18)33139-8 pubmed: 30722955
DeSantis CE, Miller KD, Dale W, et al. Cancer statistics for adults aged 85 years and older, 2019. CA Cancer J Clin. 2019;69:452–67.
doi: 10.3322/caac.21577 pubmed: 31390062
Clavien PA, Barkun J, de Oliveira ML, et al. The Clavien-Dindo classification of surgical complications: five-year experience. Ann Surg. 2009;250:187–96.
doi: 10.1097/SLA.0b013e3181b13ca2 pubmed: 19638912
Seymour CW, Liu VX, Iwashyna TJ, et al. Assessment of clinical criteria for sepsis: for the Third International Consensus Definitions for Sepsis and Septic Shock (Sepsis-3). JAMA. 2016;315:762–74.
doi: 10.1001/jama.2016.0288 pubmed: 26903335 pmcid: 5433435
Ostermann M, Joannidis M. Acute kidney injury 2016: diagnosis and diagnostic workup. Crit Care London Engl. 2016;20:299.
doi: 10.1186/s13054-016-1478-z
Cederholm T, Jensen GL, Correia MITD, et al. GLIM criteria for the diagnosis of malnutrition: a consensus report from the global clinical nutrition community. Clin Nutr. 2019;38:1–9.
doi: 10.1016/j.clnu.2018.08.002 pubmed: 30181091
Apfel CC, Läärä E, Koivuranta M, et al. A simplified risk score for predicting postoperative nausea and vomiting: conclusions from cross-validations between two centers. Anesthesiology. 1999;91:693–700.
doi: 10.1097/00000542-199909000-00022 pubmed: 10485781
Zhu AC-C, Agarwala A, Bao X. Perioperative fluid management in the enhanced recovery after surgery (ERAS) pathway. Clin Colon Rectal Surg. 2019;32:114–20.
doi: 10.1055/s-0038-1676476 pubmed: 30833860 pmcid: 6395091
Lambaudie E, de Nonneville A, Brun C, et al. Enhanced recovery after surgery program in gynaecologic oncological surgery in a minimally invasive techniques expert center. BMC Surg. 2017;17:136.
doi: 10.1186/s12893-017-0332-9 pubmed: 29282059 pmcid: 5745717
Meillat H, Braticevic C, Zemmour C, et al. Real-world implementation of a geriatric-specific ERAS protocol in patients undergoing colonic cancer surgery. Eur J Surg Oncol. 2021;47:1012–8.
doi: 10.1016/j.ejso.2020.11.128 pubmed: 33261952
Cazenave L, Faucher M, Tourret M, et al. Intravenous lidocaine and cancer outcomes after radical cystectomy. Eur J Anaesthesiol. 2022;39:396–9.
doi: 10.1097/EJA.0000000000001559 pubmed: 35232940
Anon. Fichier des décès de l’Insee. https://arbre.app/insee (Accessed Jul.10 2022).
POSE Study Group. Peri-interventional outcome study in the elderly in Europe: a 30-day prospective cohort study. Eur J Anaesthesiol. 2022;39:198–209.
doi: 10.1097/EJA.0000000000001639
Moonesinghe SR, Harris S, Mythen MG, et al. Survival after postoperative morbidity: a longitudinal observational cohort study. Br J Anaesth. 2014;113:977–84.
doi: 10.1093/bja/aeu224 pubmed: 25012586 pmcid: 4235571
Audisio RA, Bozzetti F, Gennari R, et al. The surgical management of elderly cancer patients. Eur J Cancer. 2004;40:926–38.
doi: 10.1016/j.ejca.2004.01.016 pubmed: 15093567
Ramesh H, Pope D, Gennari R, et al. No title found. World J Surg Oncol. 2005;3:17.
doi: 10.1186/1477-7819-3-17 pubmed: 15788092 pmcid: 1079964
Thomas MN, Kufeldt J, Kisser U, et al. Effects of malnutrition on complication rates, length of hospital stay, and revenue in elective surgical patients in the G-DRG-system. Nutr Burbank Los Angeles County Calif. 2016;32:249–54.
doi: 10.1016/j.nut.2015.08.021
Abunnaja S, Cuviello A, Sanchez JA. Enteral and parenteral nutrition in the perioperative period: state of the art. Nutrients. 2013;5:608–23.
doi: 10.3390/nu5020608 pubmed: 23429491 pmcid: 3635216
Jang RW, Caraiscos VB, Swami N, et al. Simple prognostic model for patients with advanced cancer based on performance status. J Oncol Pract. 2014;10:e335–41.
doi: 10.1200/JOP.2014.001457 pubmed: 25118208
Minnella EM, Awasthi R, Loiselle S-E, et al. Effect of exercise and nutrition prehabilitation on functional capacity in esophagogastric cancer surgery: a randomized clinical trial. JAMA Surg. 2018;153:1081–9.
doi: 10.1001/jamasurg.2018.1645 pubmed: 30193337 pmcid: 6583009
Hughes MJ, Hackney RJ, Lamb PJ, et al. Prehabilitation before major abdominal surgery: a systematic review and meta-analysis. World J Surg. 2019;43:1661–8.
doi: 10.1007/s00268-019-04950-y pubmed: 30788536
Penning Y, El Asmar A, Moreau M, et al. Evaluation of the Comprehensive Geriatric Assessment (CGA) tool as a predictor of postoperative complications following major oncological abdominal surgery in geriatric patients. PLoS One. 2022;17:e0264790.
doi: 10.1371/journal.pone.0264790 pubmed: 35239731 pmcid: 8893608
Fagard K, Leonard S, Deschodt M, et al. The impact of frailty on postoperative outcomes in individuals aged 65 and over undergoing elective surgery for colorectal cancer: a systematic review. J Geriatric Oncol. 2016;7:479–91.
doi: 10.1016/j.jgo.2016.06.001
Neuman HB, Weiss JM, Leverson G, et al. Predictors of short-term postoperative survival after elective colectomy in colon cancer patients ≥80 years of age. Ann Surg Oncol. 2013;20:1427–35 https://doi.org/10.1245/s10434-012-2721-8 .
doi: 10.1245/s10434-012-2721-8 pubmed: 23292483 pmcid: 3799845
Desai N, Schofield N, Richards T. Perioperative patient blood management to improve outcomes. Anesthesia Analgesia. 2018;127:1211–20.
doi: 10.1213/ANE.0000000000002549 pubmed: 29064875
Jacquemin M, Mokart D, Faucher M, et al. Late postpancreaticoduodenectomy hemorrhage: incidence, risk factors, management, and outcome. Shock Augusta GA. 2022;58:374–83.
doi: 10.1097/SHK.0000000000001999 pubmed: 36445230
Mokart D, Merlin M, Sannini A, et al. Procalcitonin, interleukin-6, and systemic inflammatory response syndrome (SIRS): early markers of postoperative sepsis after major surgery. Br J Anaesth. 2005;94:767–73.
doi: 10.1093/bja/aei143 pubmed: 15849208
Hamon A, Mokart D, Pouliquen C, et al. Intraoperative hemorrhagic shock in cancer surgical patients: short- and long-term mortality and associated factors. Shock Augusta GA. 2020;54:659–66.
doi: 10.1097/SHK.0000000000001537 pubmed: 32205792
Hatton GE, McNutt MK, Cotton BA, et al. Age-dependent association of occult hypoperfusion and outcomes in trauma. J Am Coll Surg. 2020;230:417–25.
doi: 10.1016/j.jamcollsurg.2019.12.011 pubmed: 31954820 pmcid: 7719288
Mokart D, Giaoui E, Barbier L, et al. Postoperative sepsis in cancer patients undergoing major elective digestive surgery is associated with increased long-term mortality. J Crit Care. 2016;31:48–53.
doi: 10.1016/j.jcrc.2015.10.001 pubmed: 26507291
Lambaudie E, Mathis J, Zemmour C, et al. Prediction of early discharge after gynaecological oncology surgery within ERAS. Surg Endosc. 2020;34:1985–93.
doi: 10.1007/s00464-019-06974-w pubmed: 31309314
Ji H-B, Zhu W-T, Wei Q, et al. Impact of enhanced recovery after surgery programs on pancreatic surgery: a meta-analysis. World J Gastroenterol. 2018;24:1666–78.
doi: 10.3748/wjg.v24.i15.1666 pubmed: 29686474 pmcid: 5910550
Tejedor P, Pastor C, Gonzalez-Ayora S, et al. Short-term outcomes and benefits of ERAS program in elderly patients undergoing colorectal surgery: a case-matched study compared to conventional care. Int J Colorect Dis. 2018;33:1251–8.
doi: 10.1007/s00384-018-3057-z

Auteurs

Julie Canac (J)

Département d'anesthésie et de Réanimation, Institut Paoli-Calmettes, Marseille, France.

Marion Faucher (M)

Département d'anesthésie et de Réanimation, Institut Paoli-Calmettes, Marseille, France.

Fanny Depeyre (F)

Département d'anesthésie et de Réanimation, Institut Paoli-Calmettes, Marseille, France.

Maxime Tourret (M)

Département d'anesthésie et de Réanimation, Institut Paoli-Calmettes, Marseille, France.

Marie Tezier (M)

Département d'anesthésie et de Réanimation, Institut Paoli-Calmettes, Marseille, France.

Sylvie Cambon (S)

Département d'anesthésie et de Réanimation, Institut Paoli-Calmettes, Marseille, France.

Florence Ettori (F)

Département d'anesthésie et de Réanimation, Institut Paoli-Calmettes, Marseille, France.

Luca Servan (L)

Département d'anesthésie et de Réanimation, Institut Paoli-Calmettes, Marseille, France.

Jurgita Alisauskaite (J)

Département d'anesthésie et de Réanimation, Institut Paoli-Calmettes, Marseille, France.

Camille Pouliquen (C)

Département d'anesthésie et de Réanimation, Institut Paoli-Calmettes, Marseille, France.

Frédéric Gonzalez (F)

Département d'anesthésie et de Réanimation, Institut Paoli-Calmettes, Marseille, France.

Magali Bisbal (M)

Département d'anesthésie et de Réanimation, Institut Paoli-Calmettes, Marseille, France.

Antoine Sannini (A)

Département d'anesthésie et de Réanimation, Institut Paoli-Calmettes, Marseille, France.

Jean Manuel de Guibert (JM)

Département d'anesthésie et de Réanimation, Institut Paoli-Calmettes, Marseille, France.

Eric Lambaudie (E)

Département de Chirurgie, Institut Paoli Calmette, Marseille, France.

Olivier Turrini (O)

Département de Chirurgie, Institut Paoli Calmette, Marseille, France.

Laurent Chow-Chine (L)

Département d'anesthésie et de Réanimation, Institut Paoli-Calmettes, Marseille, France.

Djamel Mokart (D)

Département d'anesthésie et de Réanimation, Institut Paoli-Calmettes, Marseille, France. mokartd@ipc.unicancer.fr.

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