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. 2022 Sep 21;407(8):3587–3597. doi: 10.1007/s00423-022-02688-1

Short-term outcomes of colorectal cancer surgery in older patients: a novel nomogram predicting postoperative morbi-mortality

David Moro-Valdezate 1,2,, José Martín-Arévalo 1,2, Óscar Ferro-Echevarría 2, Vicente Pla-Martí 1,2, Stephanie García-Botello 1,2, Leticia Pérez-Santiago 1, Ricardo Gadea-Mateo 1, Noelia Tarazona 3, Desamparados Roda 3, Susana Roselló-Keränen 3, Alejandro Espí-Macías 1,2
PMCID: PMC9722849  PMID: 36129528

Abstract

Purpose

To analyze short-term outcomes of curative-intent cancer surgery in all adult patients diagnosed with colorectal cancer undergoing surgery from January 2010 to December 2019 and determine risk factors for postoperative complications and mortality.

Methods

Retrospective study conducted at a single tertiary university institution. Patients were stratified by age into two groups: < 75 years and ≥ 75 years. Primary outcome was the influence of age on 30-day complications and mortality. Independent risk factors for postoperative adverse events or mortality were analyzed, and two novel nomograms were constructed.

Results

Of the 1486 patients included, 580 were older (≥ 75 years). Older subjects presented more comorbidities and tumors were located mainly in right colon (45.7%). After matching, no between-group differences in surgical postoperative complications were observed. The 30-day mortality rate was 5.3% for the older and 0.8% for the non-older group (p < 0.001). In multivariable analysis, the independent risk factors for postoperative complications were peripheral vascular disease, chronic pulmonary disease, severe liver disease, postoperative transfusion, and surgical approach. Independent risk factors for 30-day mortality were age ≥ 80 years, cerebrovascular disease, severe liver disease, and postoperative transfusion. The model was internally and externally validated, showing high accuracy.

Conclusion

Patients aged ≥ 75 years had similar postoperative complications but higher 30-day mortality than their younger counterparts. Patients with peripheral vascular disease, chronic pulmonary disease, or severe liver disease should be informed of higher postoperative complications. But patients aged ≥ 80 suffering cerebrovascular disease, severe liver disease, or needing postoperative transfusion should be warned of significantly increased risk of postoperative mortality.

Supplementary information

The online version contains supplementary material available at 10.1007/s00423-022-02688-1.

Keywords: Colorectal cancer, Older patients, Morbidity, Mortality, Risk factors, Nomograms

Introduction

Against the background of the progressive ageing of the European population, currently 9.84% of the Spanish population is ≥ 75 years old, and Spain is estimated to become one of the longest-living countries in Europe within 40 years [1]. This trend has serious implications, as older patients needing a surgical resection for colorectal cancer (CRC) are more likely than the non-older to present with medical and surgical postoperative complications [2, 3], probably due to the fact that comorbidities are more frequent and serious in older age patients [46]. Surgeons are therefore faced with difficult decisions when managing increasingly older patients. It is estimated that postoperative adverse outcomes in this patient subgroup could be substantial, ranging from 6 to 50% [712]. Higher postoperative mortality rates of up to 20% have also been reported in older patients, mainly during the first 30 days after surgery [4, 5, 9, 1116].

However, age may not be the only variable influencing surgical outcomes in the older. Indeed, some studies found no significant differences in rates of postoperative complications, reoperations, or mortality between patients over or under 80 years of age [6, 13, 1719]. Several factors have been identified that could increase the risk of postoperative adverse events in older patients: comorbidities, male sex, tumor location, operation time, open surgery, and emergent surgery. Interestingly, age has not appeared as a factor increasing postoperative complications or mortality rate [12, 14, 1721]. Some authors have reported comorbidities as the strongest predictors of postoperative complications in aged patients [8]. Preoperative identification of predictors of surgical complications in older patients could be useful for implementing additional optimization bundles before major surgery.

The aim of this study was to assess postoperative outcomes after curative-intent oncologic surgery for CRC and determine independent risk factors for complications or mortality during the first 30 post-surgery days.

Materials and methods

Study design and setting

This observational study included all adult patients diagnosed with CCR from January 2010 to December 2019 at the Colorectal Surgery Department in a tertiary university institution (University Clinic Hospital of Valencia, Spain). The STROBE guidelines were followed [22]. Tumors were staged according to the 8th edition of the American Joint Committee on Cancer classification. The inclusion criteria were age over 18 years, histological diagnosis of stages I-III colon or rectal adenocarcinoma, indication for elective oncological surgery with curative intent and minimum follow-up of 1 year. Exclusion criteria were appendicular tumor and local rectal excision. Patients were stratified according to significant age-specific cut-off points for this series. The older cohort was matched to the young cohort by propensity score analysis to obtain two comparable patient groups.

Data source and study variables

Patient data were acquired from hospital and primary care clinical records. Patient variables were age, sex, American Society of Anesthesiologists (ASA) score, and comorbid conditions. Patients with severe comorbidities were those with an ASA score of III-IV. Surgery-related variables were surgical procedure (right colectomy, left colectomy, segmental splenic flexure resection, total colectomy, low anterior resection, abdominoperineal resection), surgical approach (laparoscopic or open surgery), duration of operation, anastomosis, and diverting stoma. Tumor variables were tumor location, TNM classification, stage, and grade of differentiation.

Study endpoints and outcome variables

The study endpoint was the impact of age on short-term postoperative results. Outcome variables were complications and mortality during 30 days after the intervention, comparing patient cohorts according to the age-specific cut-off point, including analysis of possible risk factors for postoperative adverse events or mortality. The variable Any complication was defined as any deviation from the normal postoperative course. Adverse outcomes were divided into medical and surgical complications. Clavien-Dindo classification was used to stratify postoperative complications (severe complications were those with a score ≥ III).

Ethics

The study was approved by the local Research Ethics Committee. Informed consent was waived because of the retrospective nature of the study, and the analysis used anonymous clinical data.

Statistical analysis

A descriptive analysis of each variable of the sample was carried out. The normality of the variables was determined by graphic methods. The description of the series was conducted according to age groups. Quantitative variables were expressed as median and range and qualitative variables as percentages. The ASA score was dichotomized to assess the risk factors of the outcome variables. Cut-off points were determined with ROC curves, considering the maximum sensibility and specificity value. Propensity score matching (PSM) was used to minimize potential selection bias. The cohort of older patients was matched to the younger cohort with a ratio 1:1. The confounding variables to calculate the PSM were sex, ASA score, tumor location, surgical procedure, laparoscopic surgery, duration of operation, and diverting stoma. Logistic regression without substitution as an estimation and nearest-neighbor pairing algorithm was performed, using 0.2 of the logarithm of the PSM standard deviation as the caliber (Supplementary File 1). After the PSM, Fisher’s exact test or χ2 tests were used to find possible differences between qualitative variables, while the Mann–Whitney U test was used for quantitative variables. Multivariable analysis with logistic binary regression was conducted to identify independent risk factors for postoperative complications or mortality. Internal validation of the model was performed. External validation was conducted with a sample division validation technique that randomly assigned patients into two subgroups. The model was performed with the training subset, which was 70% of the sample randomly selected, and the test subset was the remaining 30%. ROC curves and forest plots were obtained from the model. Finally, a nomogram was built according to the validated model. P value < 0.05 was considered statistically significant. Statistical analysis was performed using IBM SPSS Statistics for Macintosh, version 25 (IBM Corp., Armonk, N.Y., USA) and R Core Team, 2020 (R Foundation for Statistical Computing, Vienna, Austria).

Results

Descriptive analysis

A total of 1486 patients diagnosed with CCR were included in the study across a period of 10 years. Median patient age was 71.0 years (range: 31–95 years). Two different significant age-specific cut-off points were obtained by analyzing the influence of age on postoperative outcomes: 75 years for postoperative complications and 80 years for postoperative mortality. Patients were therefore stratified up to age 75 for sample description and analysis of complications and clustered according to age 80 for mortality assessment. Patients’ characteristics and surgery details are outlined in Tables 1 and 2 by age group. Patients aged over 75 years presented with comorbidities more frequently than non-older subjects. The tumor was more frequently located in the rectum in patients under 75 years (43.3%), whereas the ascending and transverse colon was the most frequent tumor location in the over-75s cohort (45.7%, p < 0.001). Consequently, the non-older group predominantly underwent low anterior resection of the rectum (36.1%), while in the older the main intervention was right colectomy (44.8%, p < 0.001). Anastomosis and diverting stoma were more frequently performed in the under-75s patient subset (89.4% vs. 84.8%; p < 0.001 and 20.1% vs. 9.8%, p < 0.001; respectively). Regarding tumor staging, stages II and III were more common among older patients. Given the significant differences found between the two cohorts, PSM was performed and two completely comparable groups of 438 patients were obtained.

Table 1.

Patient characteristics by age group before and after propensity score matching

Before propensity score matching After propensity score matching
Variable Age < 75 yr. (n = 906) Age ≥ 75 yr. (n = 580) Age < 75 yr. (n = 438) Age ≥ 75 yr. (n = 438)
Value Value p Value Value p
Age (years) 64.5 (31–74) 80.0 (75–95)  < 0.001 64.7 (34–74) 79.0 (75–95)  < 0.001
Sex

  Male

  Female

551 (60.8)

355 (39.2)

318 (54.8)

262 (45.2)

0.023

264 (60.3)

174 (39.7)

245 (55.9)

193 (44.1)

0.218
ASA score < 0.001 0.928
  I 100 (11.0) 12 (2.1) 10 (2.3) 12 (2.7)
  II 509 (56.2) 184 (31.7) 178 (40.6) 183 (41.8)
  III 282 (31.1) 358 (61.7) 236 (53.9) 231 (52.7)
  IV 15 (1.7) 26 (4.5) 14 (3.2) 12 (2.7)
Comorbid conditions
  Myocardial infarction 35 (3.9) 36 (6.2) 0.046 25 (5.7) 22 (5.0) 0.765
  Congestive heart failure 17 (1.9) 45 (7.8)  < 0.001 13 (3.0) 30 (6.8) 0.012
  Peripheral vascular disease 24 (2.6) 13 (2.2) 0.734 14 (3.2) 12 (2.7) 0.843
  Cerebrovascular disease 27 (3.0) 38 (6.6) 0.002 18 (4.1) 28 (6.4) 0.172
  Dementia 4 (0.4) 40 (6.9)  < 0.001 3 (0.7) 26 (5.9)  < 0.001
  Chronic pulmonary disease 107 (11.8) 88 (15.2) 0.070 58 (13.2) 65 (14.8) 0.560
  Peptic ulcer disease 22 (2.4) 13 (2.2) 0.863 15 (3.4) 11 (2.5) 0.551
  Mild liver disease 41 (4.5) 14 (2.4) 0.035 21 (4.8) 11 (2.5) 0.104
  Diabetes without chronic complication 194 (21.4) 171 (29.5)  < 0.001 122 (27.9) 127 (29.0) 0.765
  Diabetes with chronic complication 5 (0.6) 3 (0.5) 1.000 3 (0.7) 2 (0.5) 1.000
  Renal disease 28 (3.1) 49 (8.4)  < 0.001 24 (5.5) 34 (7.8) 0.221
  Severe liver disease 15 (1.7) 11 (1.9) 0.840 10 (2.3) 8 (1.8) 0.813
Tumor location < 0.001 0.769
  Right and transverse colon 236 (26.0) 265 (45.7) 161 (36.8) 151 (34.5)
  Left and sigmoid colon 274 (30.2) 158 (27.2) 128 (29.2) 142 (32.4)
  Upper rectum 140 (15.5) 57 (9.8) 55 (12.6) 55 (12.6)
  Low rectum 252 (27.8) 58 (10.0) 94 (21.5) 90 (20.5)

Statistics presented as median (min–max) or n (%). p-values: Mann–Whitney test, Pearson’s χ2 test, Fisher´s exact test

ASA American Society of Anesthesiologists

Boldface was used to highlight those significative p-values (lower than 0.05)

Table 2.

Characteristics of surgery and histopathologic findings by age group before and after propensity score matching

Before propensity score matching After propensity score matching
Variable Age < 75 yr. (n = 906) Age ≥ 75 yr. (n = 580) Age < 75 yr. (n = 438) Age ≥ 75 yr. (n = 438)
Value Value p Value value p
Surgical procedure < 0.001 0.902
  Right colectomy 218 (24.1) 260 (44.8) 150 (34.2) 147 (33.6)
  Left colectomy 247 (27.3) 126 (21.7) 106 (24.2) 111 (25.3)
  Segmental splenic flexure resection 7 (0.8) 8 (1.4) 7 (1.6) 5 (1.1)
  Total colectomy 41 (4.5) 29 (5.0) 20 (4.6) 24 (5.5)
  Low anterior resection 327 (36.1) 125 (21.6) 128 (29.2) 119 (27.2)
  Abdominoperineal resection 66 (7.3) 32 (5.5) 27 (6.2) 32 (7.3)
Laparoscopic surgery 417 (46.0) 264 (45.5) 0.873 197 (45.0) 205 (46.8) 0.635
Duration of operation (min.) 180 (50–600) 150 (47–520)  < 0.001 160 (50–600) 150 (47–520) 0.112
Anastomosis 810 (89.4) 492 (84.8) 0.010 388 (88.6) 372 (84.9) 0.135
Diverting stoma 182 (20.1) 57 (9.8)  < 0.001 63 (14.4) 51 (11.6) 0.269
Neoadjuvant treatment for rectal cancer 165 (18.2) 66 (11.4)  < 0.001 51 (11.6) 46 (10.5) 0.789
Local invasion (AJCC) < 0.001 0.431
  pT1 159 (17.5) 68 (11.7) 78 (17.8) 62 (14.2)
  pT2 201 (22.2) 104 (17.9) 84 (19.2) 91 (20.8)
  pT3 423 (46.7) 307 (52.9) 208 (47.5) 222 (50.7)
  pT4 123 (13.6) 101 (17.4) 68 (15.5) 63 (14.4)
Lymph node metastases (AJCC) 0.344 0.344
  pN0 631 (69.6) 383 (66.0) 305 (69.6) 285 (65.1)
  pN1 199 (22.0) 143 (24.7) 99 (22.6) 112 (25.6)
  pN2 76 (8.4) 54 (9.3) 34 (7.8) 41 (9.4)
Tumor stage (AJCC) < 0.001 0.342
  I 306 (33.8) 142 (24.5) 137 (31.3) 125 (28.5)
  II 326 (36.0) 239 (41.2) 168 (38.4) 160 (36.5)
  III 274 (30.2) 199 (34.3) 133 (30.4) 153 (34.9)
Grade of tumor differentiation 0.074 0.613
  High 179 (19.8) 114 (19.7) 91 (20.8) 89 (20.3)
  Moderate 685 (75.6) 437 (75.3) 323 (73.7) 331 (75.6)
  Low 29 (5.0) 42 (4.6) 24 (5.5) 18 (4.1)

Statistics presented as median (min–max) or n (%). p-values: Mann–Whitney test, Pearson’s χ2 test, Fisher’s exact test

AJCC American Joint Committee on Cancer, 8th edition (2018)

Boldface was used to highlight those significative p-values (lower than 0.05)

Surgery outcomes

In the cohort of non-older patients, a total of 263 patients (29.0%) presented postoperative complications during the 30 postoperative days, while 39.0% of the older patients suffered any postoperative adverse event (p < 0.001). Table 3 shows surgery outcomes. After matching the two age cohorts, the only differences found between them were in respiratory and cardiac complications. Only cases with anastomosis were included in the analysis of anastomotic failure, without between-group differences. Postoperative transfusion was needed more frequently in patients aged ≥ 75 years. According to the Clavien-Dindo classification, older patients suffered severe complications (≥ III) more often than the younger subset (16.2% vs 11.9%, p < 0.001). The postoperative mortality rate was 2.5% across the whole series. Patients aged ≥ 80 years presented a higher mortality rate during the first 30 postoperative days than those aged under that cutoff (5.3% vs. 0.8%, respectively; p < 0.001) and after matching the two cohorts, these differences remained (p = 0.024).

Table 3.

Surgery outcomes before and after propensity score matching

Before propensity score matching After propensity score matching
Variable Age < 75 yr. (n = 906) Age ≥ 75 yr. (n = 580) Age < 75 yr. (n = 438) Age ≥ 75 yr. (n = 438)
Value Value p Value Value p
Length of stay (days) 8 (1–311) 8 (1–89)  < 0.001 8 (1–154) 8 (1–89) 0.021
Any complication during the episode (30 days) 263 (29.0) 226 (39.0)  < 0.001 138 (31.5) 165 (37.7) 0.065
Medical complications during the episode (30 days) 68 (7.5) 95 (16.4) < 0.001 42 (9.6) 72 (16.4) 0.003
  Respiratory complications 30 (3.3) 64 (11.0)  < 0.001 20 (4.6) 46 (10.5)  < 0.001
  Cardiac complications 17 (1.9) 35 (6.0)  < 0.001 12 (2.7) 26 (5.9) 0.030
  Urinary complications 38 (4.2) 28 (4.8) 0.606 20 (4.6) 23 (5.3) 0.755
  Cerebrovascular accident 2 (0.2) 3 (0.5) 0.384 2 (0.5) 1 (0.2) 1.000
  Upper gastrointestinal bleeding 1 (0.1) 3 (0.5) 0.306 1 (0.2) 3 (0.7) 0.624
Surgical complications during the episode (30 days) 229 (25.3) 177 (30.5) 0.027 117 (26.7) 131 (29.9) 0.330
  Surgical site infection 126 (13.9) 89 (15.3) 0.450 69 (15.8) 67 (15.3) 0.926
  Superficial 28 (3.1) 15 (2.6) 0.636 18 (4.1) 14 (3.2) 0.590
  Deep 7 (0.8) 4 (0.7) 1.000 4 (0.9) 3 (0.7) 1.000
  Organ space 42 (4.6) 29 (5.0) 0.803 19 (4.3) 20 (4.6) 1.000
  Ileus 76 (8.4) 66 (11.4) 0.058 34 (7.8) 44 (10.0) 0.286
  Anastomotic leak 57 (6.3) 44 (7.6) 0.343 30 (6.8) 34 (7.8) 0.697
  Enterocutaneous fistula 17 (1.9) 5 (0.9) 0.128 3 (0.7) 5 (1.1) 0.725
  Wound disruption 14 (1.5) 21 (3.6) 0.013 10 (2.3) 15 (3.4) 0.418
  Postoperative bleeding 6 (0.7) 8 (1.4) 0.177 2 (0.5) 6 (1.4) 0.287
  Intestinal ischaemia 7 (0.8) 5 (0.9) 1.000 4 (0.9) 5 (1.1) 1.000
  Stoma complications 5 (0.6) 7 (1.2) 0.234 4 (0.9) 7 (1.6) 0.546
  Intestinal perforation 3 (0.3) 2 (0.3) 1.000 2 (0.5) 1 (0.2) 1.000
  Iatrogenic urinary lesions 3 (0.3) 0 (0.0) 0.524 2 (0.5) 0 (0.0) 0.499
Perioperative transfusion 61 (6.7) 71 (12.2)  < 0.001 39 (8.9) 51 (11.6) 0.221
Postoperative transfusion 96 (10.6) 108 (18.6)  < 0.001 53 (12.1) 80 (18.3) 0.014
Reoperation 71 (7.8) 62 (10.7) 0.063 39 (8.9) 47 (10.7) 0.427
Readmission 27 (3.0) 6 (1.0) 0.012 13 (3.0) 5 (1.1) 0.093
Clavien-Dindo classification < 0.001 0.015
  0 643 (71.0) 354 (61.0) 300 (68.5) 273 (62.3)
  I 60 (6.6) 43 (7.4) 38 (8.7) 36 (8.2)
  II 89 (9.8) 58 (10.0) 38 (8.7) 41 (9.4)
  IIIa 28 (3.1) 12 (2.1) 13 (3.0) 10 (2.3)
  IIIb 45 (5.0) 32 (5.5) 23 (5.3) 22 (5.0)
  IVa 26 (2.9) 37 (6.4) 18 (4.1) 31 (7.1)
  IVb 8 (0.9) 13 (2.2) 4 (0.9) 10 (2.3)

Statistics presented as median (min–max) or n (%)

p-values: Mann–Whitney test, Pearson’s χ2 test, Fisher’s exact test

Boldface was used to highlight those significative p-values (lower than 0.05)

Risk factors for postoperative complications

We conducted univariable and multivariable analysis of factors associated with postoperative complications. As depicted in the forest plot (Fig. 1), binary logistic regression revealed independent risk factors for presenting any complication to be peripheral vascular disease, chronic pulmonary disease, severe liver disease, and postoperative transfusion. However, the laparoscopic approach was an independent factor predicting a lower postoperative complication rate. All these factors showed a variance inflation factor under 1.5. The model had an area under the curve of 0.69 (IC 95% = 0.65–0.73) and 70.3% accuracy. Age was not an independent risk factor for postoperative complications and moreover showed no association with surgical site infection (p = 0.181), anastomotic leak (p = 0.636), or reoperation rate (p = 0.195).

Fig. 1.

Fig. 1

Multivariable analysis model for postoperative complications. A: Forest plot of independent risk factors. B: Receiver operating characteristic curves of the model

Risk factors for postoperative mortality

The forest plot of Fig. 2 represents independent risk factors for postoperative mortality obtained from multivariable analysis with binary logistic regression: age ≥ 80 years, cerebrovascular disease, severe liver disease, and postoperative transfusion. Variance inflation factor was lower than 1.3 in all factors. The model presented an area under the curve of 0.90 (IC 95% = 0.83–0.95) and an accuracy of 93.9%.

Fig. 2.

Fig. 2

Multivariable analysis model for 30-day mortality. A: Forest plot of independent risk factors. B: Receiver operating characteristic curves of the model

Nomograms

Two nomograms were constructed to predict the risk of complications and mortality during the postoperative period (Figs. 3, 4). The value of each risk factor is obtained from the upper percentile line, and their sum gives an overall score indicating the probability of postoperative complications or 30-day mortality in the risk line at the bottom. The prognostic nomogram of postoperative complications after colorectal cancer surgery showed an accuracy of 68.4% with an area under the ROC curve of 70%, and the prognostic nomogram of 30-day mortality was able to predict postoperative mortality with an accuracy of 90.2% and an area under the ROC curve of 91%.

Fig. 3.

Fig. 3

Prognostic nomogram of postoperative complications after colorectal cancer surgery

Fig. 4.

Fig. 4

Prognostic nomogram of 30-day mortality after colorectal cancer surgery

Discussion

This is one of the few studies to focus on analysis of independent risk factors for postoperative complications and mortality, employing a substantial sample size with detailed perioperative data and providing a novel nomogram to predict short-term outcomes.

To establish two age groups, the age-specific cut-off point of ≥ 75 years was fitted for the present series, thus providing non-arbitrary sample stratification. In most previous published studies, there is great variability between the age thresholds selected for postoperative outcomes in older patients; they are usually standard cut-off points, not representing inflection points in the series and without medical or biological evidence to support the choice. Some authors also found that age ≥ 75 years could be an optimal cut-off, and age has also been stated as a significant risk factor for postoperative complications in colorectal surgery [12]. After analyzing data on physical and psychological health in the older, the Japanese Geriatrics Society proposed that elderly should be defined as those aged 75 years and older [23]. Nevertheless, other authors classified older patients into three groups: youngest-old (65 to 74 years), middle-old (75 to 84 years) and oldest-old (≥ 85 years) [24].

Comparing the two age groups, older patients had a greater number of comorbidities, which were more also severe. Improvements in perioperative multidisciplinary care have made colorectal surgery feasible in the older despite the fact that they frequently present with serious comorbidities [46]. Similar to other available studies, in the aged cohort, the tumor was more frequently located in the ascending colon, resulting in a higher ratio of right colectomies [6, 16]. As the two subsets differed in their baseline features, PSM was conducted to obtain two homogeneous groups in order to compare postoperative outcomes. Note that all study patients included received the same perioperative bundle of enhanced recovery after surgery protocols, regardless of age.

Similarly to other authors, we found no differences between older and younger patients in postoperative complication rates, including anastomotic leak [6, 13]. These results support that in patients eligible for colorectal resection, a primary anastomosis can be performed safely without excess risk. A recent systematic review and meta-analysis conducted by Hoshino et al,. focusing on the outcomes of laparoscopic surgery for CCR in older patients, reported slightly higher incidence of postoperative complications in the older, but without differences in anastomotic leak or mortality rates [10].

Our findings revealed that severe postoperative complications were mainly due to worsening of previous comorbidities. Cardiopulmonary complications were more frequent among patients aged ≥ 75 years. Chan et al. also reported pneumonia with respiratory failure as the most common postoperative complication and the leading cause of mortality [17]. In a study of over 1200 CCR patients aged ≥ 85 years undergoing surgical resection, Verweij et al. found high rates of cardiopulmonary complications and excess mortality, particularly in the first year after surgery [11].

The mortality rate for older patients during the postoperative period was 5.3%, in line with outcomes obtained in other studies on octogenarians (2%–13%) and nonagenarians (2%–20%) [4, 5, 9, 1116]. Although older patients may present more comorbidities, several studies found no differences in short-term postoperative reoperations or mortality after colorectal surgery [1719]. Improvements in mortality rates are likely because of advances in perioperative care, safe standardized minimally invasive procedures and better patient selection for surgery. In our experience, although colorectal resection did not involve higher postoperative complication rates in older patients, it did entail higher mortality rates, predominantly in patients with associated comorbidities. Prehabilitation programs could help to optimize preoperative patient status, minimize postoperative risks, and improve surgical outcomes. Furthermore, aged patients without concurrent diseases can be successfully treated by curative-intent surgery. Comorbidities may therefore have more impact on postoperative outcomes than age itself.

Age has long been considered among the predominant risk factors for postoperative complications, but essentially due to an increased number of comorbid conditions and worse functional status [4, 11, 12]. Likewise, multivariable analysis revealed that several comorbidities, but not age, were independent predictors of postoperative complications. Moreover, age did not present any association with surgical site infection, anastomotic leak, or with reoperation rate. These findings are consistent with those obtained from other large series, where age was not predictive of in-hospital complications or mortality, suggesting that other conditions may impact more significantly in surgical outcomes [8, 12, 14, 19, 20, 25]. Therefore, it would be more appropriate to consider a frailty index rather than age in preoperative decision-making. Identification of predictors for surgical complications in elderly frail patients could be useful to implement further optimization bundles before major surgery.

Chronic pulmonary disease was an independent risk factor for postoperative adverse events. In other studies, preoperative cardiopulmonary function was determinant in postoperative outcomes [11, 17]. Respiratory physiotherapy is a good measure to incorporate in perioperative care for older patients, given that it could decrease incidence of postoperative pulmonary complications and 30-day mortality [26].

Severe liver disease is a serious comorbidity and was found to be independently associated with adverse postoperative outcomes. Similarly, a recent meta-analysis concluded that pre-existing liver cirrhosis was associated with higher postoperative major complication and mortality rates following CRC surgery [27]. One reason for this could be that abnormal liver metabolism leads to hepatic coagulopathy, lower albumin levels, reduced drug metabolism, and weakened immune function, increasing postoperative adverse events.

Laparoscopic surgery is safe in older patients, and moreover, postoperative complications including wound infection, ileus, and pneumonia are less frequent than in open surgery [8, 12, 18, 19, 28]. In the present series, laparoscopic approach was found to be independently associated with a lower postoperative complication rate. Similarly, a Dutch population-based study found that compared with open surgery, laparoscopic surgery was independently associated with a lower risk of cardiopulmonary complications and reduced risk of postoperative mortality in elective CCR surgery [21]. Older patients could benefit from laparoscopic surgery despite their limited life expectancy and comorbidities.

Undoubtedly one of the most interesting aspects of our study is the determination of factors influencing postoperative death. In recent years, various prognostic factors for 30-day postoperative mortality have been outlined in older patients, such as age ≥ 85 years, anemia, ASA score IV, and palliative cancer surgery [13]. We found that age ≥ 80 years, cerebrovascular disease, severe liver disease, and need for postoperative transfusion increased the risk of 30-day mortality. Interestingly, advanced age was not predictive of complications, but was revealed as a predictor for postoperative mortality. A possible explanation could be that although older patients present a similar postoperative complication rate to younger ones, recovery is more hazardous in the former group due to their limited physiological reserve, which could entail a higher risk of mortality. These outcomes are in line with those obtained by Youl et al. in a population-based study in Australia which analyzed postoperative outcomes in 18,339 patients aged over 65 years diagnosed with CRC. Among other factors such as advanced tumor stage, open procedure, and emergency surgery, age ≥ 75 years was found to be independently related with an increased risk of postoperative death [12]. Other studies have also concluded that comorbidities were the main factors influencing mortality after surgery, but age itself was not [14, 17, 25].

Another aspect frequently associated with worse postoperative complications potentially leading to increased mortality is the need for postoperative transfusion. As expected, therefore, blood transfusion was revealed as a prognostic factor for 30-day complications and mortality, consistent with the results reported in other studies [16]. Postoperative transfusion may reveal intraoperative bleeding. However, in the present series, the main indication for transfusion was the worsening of preoperative preexisting anemia. Many studies reported worse outcomes when blood transfusion was needed during the postoperative period, particularly in elderly patients. Some authors found that perioperative blood transfusion was a very good predictor of postoperative mortality [29, 30]. Older patients have limited physiological reserve, making this subset of patients especially vulnerable to the consequences of anemia, therefore preoperative optimization of hemoglobin level should be recommended.

Similarly, emergent surgery is known to negatively affect surgical outcomes and has been widely proposed as a predictor of postoperative mortality in older patients [4, 1114, 17]. In the present series, however, we included elective surgery only to diminish confounding factors in the analysis and avoid heterogeneity between groups.

The nomograms constructed in the present study are in line with the few that have previously been published. As in Kiran et al., our model was built with a 70% randomly selected study population, and the remaining 30% used to validate it. This ratio was used to avoid overfitting the model. In the multicenter national study conducted by Anaco Study Group, however, the ratio was 60/40 [31, 32]. The models presented similar areas under the curve and share some risk factors. The predictive novel nomograms developed in the present study confirm that prior severe comorbid conditions are the main factors in postoperative short-term outcomes. The nomograms presented herein are useful tools in our setting, as they easily provide individualized risk prediction of postoperative complications or mortality, can help clinicians in preoperative evaluation by providing accurate information about postoperative risks, and could facilitate enhanced, tailored multidisciplinary care to minimize complications.

The study included a relatively large sample with non-arbitrary age cut-off points and two homogeneous patient groups obtained through PSM that received the same perioperative care. The prediction model constructed obtained high accuracy and satisfactory internal and external validation and was presented in the form of a nomogram to facilitate its application by clinicians in outpatient clinics. Nonetheless, this study has some limitations, arising from its observational and retrospective design at a single institution. Patients diagnosed with rectal cancer were included in the study because after the PSM, this subgroup of patients was equally distributed between the two age groups; however, this could be a potential source of bias given that rectal surgery is more complex and time consuming than colon surgery. Data about performance status, frailty, sarcopenia, or nutritional status were not recorded, so accurate information about the functional status of the patients was limited.

Conclusion

Patients aged over 75 years with CCR who underwent oncologic surgery presented a similar complication rate but higher mortality rate than younger patients during the postoperative period. Patients with severe comorbidities (peripheral vascular disease, chronic pulmonary disease, or severe liver disease) should be informed of higher postoperative complications, regardless of age, but patients aged over 80 suffering cerebrovascular disease, or severe liver disease, or needing postoperative transfusion should be warned of a significantly increased risk of postoperative mortality. The novel nomogram proposed herein could help tailor management of patient comorbidities and target perioperative care to improve outcomes.

Supplementary information

Below is the link to the electronic supplementary material.

423_2022_2688_MOESM1_ESM.pdf (24.4KB, pdf)

Supplementary file1 Flowchart of propensity score matching of study patients. (PDF 24 KB)

Author contributions

Study conception and design: David Moro-Valdezate, José Martín-Arévalo, Óscar Ferro-Echevarría. Acquisition of data: José Martín-Arévalo, Leticia Pérez-Santiago, Óscar Ferro-Echevarría. Analysis and interpretation of data: José Martín-Arévalo, Vicente Pla-Martí, Stephanie García-Botello, Alejandro Espí-Macías. Drafting of manuscript: David Moro-Valdezate, Ricardo Gadea-Mateo, Noelia Tarazona. Critical revision of manuscript: Susana Roselló-Keränen, Alejandro Espí-Macías.

Funding

Open Access funding provided thanks to the CRUE-CSIC agreement with Springer Nature.

Data sharing

Data supporting the findings of this study are available from the corresponding author upon reasonable request.

Declarations

Ethics approval

The study was approved by the local Research Ethics Committee. Informed consent was waived because of the retrospective nature of the study, and the analysis used anonymous clinical data.

Conflict of interest

  1. David Moro-Valdezate (MD, PhD, Professor)

Payment or honoraria for lectures, presentations, speaker bureaus or educational events from Johnson & Johnson. Support for attending meetings and/or travel from Takeda.

  • 2.

    José Martín-Arévalo (MD, PhD, Professor)

Payment or honoraria for lectures, presentations, speaker bureaus or educational events from Johnson & Johnson. Support for attending meetings and/or travel from Takeda.

  • 3.

    Óscar Ferro-Echevarría (MD)

Declares no relationships, conditions or circumstances that present potential conflict of interest.

  • 4.

    Vicente Pla-Martí (MD, PhD, Professor)

Payment or honoraria for lectures, presentations, speaker bureaus or educational events from Johnson & Johnson, Medtronic and Braun Medical. Support for attending meetings and/or travel from Takeda.

  • 5.

    Stephanie García-Botello (MD, PhD, Professor)

Payment or honoraria for lectures, presentations, speaker bureaus or educational events from Johnson & Johnson.

  • 6.

    Leticia Pérez-Santiago (MD)

Declares no relationships, conditions or circumstances that present potential conflict of interest.

  • 7.

    Ricardo Gadea-Mateo (MD)

Declares no relationships, conditions or circumstances that present potential conflict of interest.

  • 8.

    Noelia Tarazona (MD, PhD)

Declares no relationships, conditions or circumstances that present potential conflict of interest.

  • 9.

    Roda Desamparados (MD, PhD)

Declares no relationships, conditions or circumstances that present potential conflict of interest.

  • 10.

    Susana Roselló-Keränen (MD, PhD)

Declares no relationships, conditions or circumstances that present potential conflict of interest.

  • 11.

    Alejandro Espí-Macías (MD, PhD, Professor)

Payment or honoraria for lectures, presentations, speaker bureaus or educational events from Johnson & Johnson, Medtronic and Braun Medical. Support for attending meetings and/or travel from Takeda.

Footnotes

Publisher's note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Contributor Information

David Moro-Valdezate, Email: david.moro@uv.es.

José Martín-Arévalo, Email: martin_jose@gva.es.

Óscar Ferro-Echevarría, Email: ferroquelato@gmail.com.

Vicente Pla-Martí, Email: vplamarti@yahoo.es.

Stephanie García-Botello, Email: stephaniegarciabotello@gmail.com.

Leticia Pérez-Santiago, Email: lety_stn@hotmail.com.

Ricardo Gadea-Mateo, Email: rgadeamateo@gmail.com.

Noelia Tarazona, Email: noetalla@incliva.es.

Desamparados Roda, Email: derope@hotmail.com.

Susana Roselló-Keränen, Email: srosello@incliva.es.

Alejandro Espí-Macías, Email: alejandro.espi@uv.es.

References

  • 1.GBD Mortality and Causes of Death Collaborators (2015) Global, regional, and national age–sex specific all-cause and cause-specific mortality for 240 causes of death, 1990–2013: a systematic analysis for the Global Burden of Disease Study 2013. The Lancet. 2013;385:117–171. doi: 10.1016/S0140-6736(14)61682-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Handforth C, Clegg A, Young C, et al. The prevalence and outcomes of frailty in older cancer patients: a systematic review. Ann Oncol. 2015;26:1091–1101. doi: 10.1093/annonc/mdu540. [DOI] [PubMed] [Google Scholar]
  • 3.Baré M, Mora L, Pera M, et al. Type and consequences of short-term complications in colon cancer surgery, focusing on the oldest old. Clin Colorectal Cancer. 2020;19:e18–e25. doi: 10.1016/j.clcc.2019.11.003. [DOI] [PubMed] [Google Scholar]
  • 4.Colorectal Cancer Collaborative Group Surgery for colorectal cancer in elderly patients: a systematic review. Lancet. 2000;356:968–974. doi: 10.1016/S0140-6736(00)02713-6. [DOI] [PubMed] [Google Scholar]
  • 5.Arenal JJ, Tinoco C, Labarga F, et al. Colorectal cancer in nonagenarians: colorectal cancer in nonagenarians. Colorectal Dis. 2012;14:44–47. doi: 10.1111/j.1463-1318.2011.02596.x. [DOI] [PubMed] [Google Scholar]
  • 6.Tokuhara K, Nakatani K, Ueyama Y, et al. Short- and long-term outcomes of laparoscopic surgery for colorectal cancer in the elderly: a prospective cohort study. Int J Surg. 2016;27:66–71. doi: 10.1016/j.ijsu.2016.01.035. [DOI] [PubMed] [Google Scholar]
  • 7.Johnston S, Louis M, Churilov L, et al. Health costs of post-operative complications following rectal resection: a systematic review. ANZ J Surg. 2020;90:1270–1276. doi: 10.1111/ans.15708. [DOI] [PubMed] [Google Scholar]
  • 8.Zeng W-G, Liu M-J, Zhou Z-X, et al. Outcomes of colorectal cancer surgery in nonagenarian patients: a multicenter retrospective study. J Gastrointest Oncol. 2021;12:1568–1576. doi: 10.21037/jgo-21-324. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Tamura K, Matsuda K, Fujita Y, et al. Optimal assessment of frailty predicts postoperative complications in older patients with colorectal cancer surgery. World J Surg. 2021;45:1202–1209. doi: 10.1007/s00268-020-05886-4. [DOI] [PubMed] [Google Scholar]
  • 10.Hoshino N, Fukui Y, Hida K, Sakai Y. Short-term outcomes of laparoscopic surgery for colorectal cancer in the elderly versus non-elderly: a systematic review and meta-analysis. Int J Colorectal Dis. 2019;34:377–386. doi: 10.1007/s00384-019-03234-0. [DOI] [PubMed] [Google Scholar]
  • 11.Verweij NM, Schiphorst AHW, Maas HA, et al. Colorectal cancer resections in the oldest old between 2011 and 2012 in The Netherlands. Ann Surg Oncol. 2016;23:1875–1882. doi: 10.1245/s10434-015-5085-z. [DOI] [PubMed] [Google Scholar]
  • 12.Youl PH, Theile DE, Moore J, et al. Outcomes following major resection for colorectal cancer in patients aged 65+ years: a population-based study in Queensland, Australia. ANZ J Surg. 2021;91:932–937. doi: 10.1111/ans.16631. [DOI] [PubMed] [Google Scholar]
  • 13.Duron J-J, Duron E, Dugue T, et al. Risk factors for mortality in major digestive surgery in the elderly: a multicenter prospective study. Ann Surg. 2011;254:375–382. doi: 10.1097/SLA.0b013e318226a959. [DOI] [PubMed] [Google Scholar]
  • 14.Ihedioha U, Gravante G, Lloyd G, et al. Curative colorectal resections in patients aged 80 years and older: clinical characteristics, morbidity, mortality and risk factors. Int J Colorectal Dis. 2013;28:941–947. doi: 10.1007/s00384-012-1626-0. [DOI] [PubMed] [Google Scholar]
  • 15.Bessems SAM, Konsten JLM, Vogelaar JFJ, et al. Frailty screening by Geriatric-8 and 4-meter gait speed test is feasible and predicts postoperative complications in elderly colorectal cancer patients. J Geriatr Oncol. 2021;12:592–598. doi: 10.1016/j.jgo.2020.10.012. [DOI] [PubMed] [Google Scholar]
  • 16.Roque-Castellano C, Fariña-Castro R, Nogués-Ramia EM, et al. Colorectal cancer surgery in selected nonagenarians is relatively safe and it is associated with a good long-term survival: an observational study. World J Surg Onc. 2020;18:120. doi: 10.1186/s12957-020-01895-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Chan TY, Foo CC, Law WL, Lo O. Outcomes of colorectal cancer surgery in the nonagenarians: 20-year result from a tertiary center. BMC Surg. 2019;19:155. doi: 10.1186/s12893-019-0623-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Peltrini R, Imperatore N, Carannante F, et al. Age and comorbidities do not affect short-term outcomes after laparoscopic rectal cancer resection in elderly patients. A multi-institutional cohort study in 287 patients. Updates Surg. 2021;73:527–537. doi: 10.1007/s13304-021-00990-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Utsumi M, Matsuda T, Yamashita K, et al. Short-term and long-term outcomes after laparoscopic surgery for elderly patients with colorectal cancer aged over 80 years: a propensity score matching analysis. Int J Colorectal Dis. 2021;36:2519–2528. doi: 10.1007/s00384-021-03973-z. [DOI] [PubMed] [Google Scholar]
  • 20.Michaud Maturana M, English WJ, Nandakumar M, et al. The impact of frailty on clinical outcomes in colorectal cancer surgery: a systematic literature review. ANZ J Surg. 2021;91:2322–2329. doi: 10.1111/ans.16941. [DOI] [PubMed] [Google Scholar]
  • 21.Gietelink L, Wouters MWJM, Bemelman WA, et al. Reduced 30-day mortality after laparoscopic colorectal cancer surgery: a population based study from the Dutch Surgical Colorectal Audit (DSCA) Ann Surg. 2016;264:135–140. doi: 10.1097/SLA.0000000000001412. [DOI] [PubMed] [Google Scholar]
  • 22.von Elm E, Altman DG, Egger M, et al. The strengthening the reporting of observational studies in epidemiology (STROBE) statement: guidelines for reporting observational studies. Int J Surg. 2014;12:1495–1499. doi: 10.1016/j.ijsu.2014.07.013. [DOI] [PubMed] [Google Scholar]
  • 23.Ouchi Y, Rakugi H, Arai H, et al. Redefining the elderly as aged 75 years and older: proposal from the Joint Committee of Japan Gerontological Society and the Japan Geriatrics Society: redefining elderly: proposal from Japan. Geriatr Gerontol Int. 2017;17:1045–1047. doi: 10.1111/ggi.13118. [DOI] [PubMed] [Google Scholar]
  • 24.Lee SB, Oh JH, Park JH, et al. Differences in youngest-old, middle-old, and oldest-old patients who visit the emergency department. Clin Exp Emerg Med. 2018;5:249–255. doi: 10.15441/ceem.17.261. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Tan KY, Kawamura Y, Mizokami K, et al. Colorectal surgery in octogenarian patients—outcomes and predictors of morbidity. Int J Colorectal Dis. 2009;24:185–189. doi: 10.1007/s00384-008-0615-9. [DOI] [PubMed] [Google Scholar]
  • 26.Odor PM, Bampoe S, Gilhooly D, Creagh-Brown B,  Moonesinghe SR (2020) Perioperative interventions for prevention of postoperative pulmonary complications: systematic review and meta-analysis. BMJ 368:m540. 10.1136/bmj.m540 [DOI] [PMC free article] [PubMed]
  • 27.Cheng Y-X, Tao W, Zhang H, et al. Does liver cirrhosis affect the surgical outcome of primary colorectal cancer surgery? A meta-analysis. World J Surg Onc. 2021;19:167. doi: 10.1186/s12957-021-02267-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Son IT, Kim JY, Kim MJ, et al. Clinical and oncologic outcomes of laparoscopic versus open surgery in elderly patients with colorectal cancer: a retrospective multicenter study. Int J Clin Oncol. 2021;26:2237–2245. doi: 10.1007/s10147-021-02009-4. [DOI] [PubMed] [Google Scholar]
  • 29.Wu W-C, Smith TS, Henderson WG, et al. Operative blood loss, blood transfusion, and 30-day mortality in older patients after major noncardiac surgery. Ann Surg. 2010;252:11–17. doi: 10.1097/SLA.0b013e3181e3e43f. [DOI] [PubMed] [Google Scholar]
  • 30.Roque-Castellano C, Marchena-Gómez J, Fariña-Castro R, et al. Perioperative blood transfusion is associated with an increased mortality in older surgical patients. World J Surg. 2016;40:1795–1801. doi: 10.1007/s00268-016-3521-2. [DOI] [PubMed] [Google Scholar]
  • 31.Sánchez-Guillén L, Frasson M, Pellino G, et al. Nomograms for morbidity and mortality after oncologic colon resection in the enhanced recovery era: results from a multicentric prospective national study. Int J Colorectal Dis. 2020;35:2227–2238. doi: 10.1007/s00384-020-03692-x. [DOI] [PubMed] [Google Scholar]
  • 32.Kiran RP, Attaluri V, Hammel J, Church J. A novel nomogram accurately quantifies the risk of mortality in elderly patients undergoing colorectal surgery. Ann Surg. 2013;257:905–908. doi: 10.1097/SLA.0b013e318269d337. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

423_2022_2688_MOESM1_ESM.pdf (24.4KB, pdf)

Supplementary file1 Flowchart of propensity score matching of study patients. (PDF 24 KB)

Data Availability Statement

Data supporting the findings of this study are available from the corresponding author upon reasonable request.


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