Next Article in Journal
Using Geovisualization Tools to Examine Attitudes towards Alcohol Exposure in Urban Environments: A Pilot Study in Madrid, Spain
Next Article in Special Issue
Age Increases the Risk of Mortality by Four-Fold in Patients with Emergent Paralytic Ileus: Hospital Length of Stay, Sex, Frailty, and Time to Operation as Other Risk Factors
Previous Article in Journal
Digital Rehabilitation for Elbow Pain Musculoskeletal Conditions: A Prospective Longitudinal Cohort Study
Previous Article in Special Issue
Mortality Risk Factors in Patients Admitted with the Primary Diagnosis of Tracheostomy Complications: An Analysis of 8026 Patients
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Adult and Elderly Risk Factors of Mortality in 23,614 Emergently Admitted Patients with Rectal or Rectosigmoid Junction Malignancy

1
School of Medicine, New York Medical College, Valhalla, NY 10595, USA
2
Westchester Medical Center, New York Medical College, Valhalla, NY 10595, USA
3
Department of Surgery, University of Arizona, Tucson, AZ 85721, USA
*
Author to whom correspondence should be addressed.
Int. J. Environ. Res. Public Health 2022, 19(15), 9203; https://doi.org/10.3390/ijerph19159203
Submission received: 30 June 2022 / Revised: 24 July 2022 / Accepted: 25 July 2022 / Published: 27 July 2022
(This article belongs to the Special Issue Hospital Length of Stay and Health Outcomes)

Abstract

:
Background: Colorectal cancer, among which are malignant neoplasms of the rectum and rectosigmoid junction, is the fourth most common cancer cause of death globally. The goal of this study was to evaluate independent predictors of in-hospital mortality in adult and elderly patients undergoing emergency admission for malignant neoplasm of the rectum and rectosigmoid junction. Methods: Demographic and clinical data were obtained from the National Inpatient Sample (NIS), 2005–2014, to evaluate adult (age 18–64 years) and elderly (65+ years) patients with malignant neoplasm of the rectum and rectosigmoid junction who underwent emergency surgery. A multivariable logistic regression model with backward elimination process was used to identify the association of predictors and in-hospital mortality. Results: A total of 10,918 non-elderly adult and 12,696 elderly patients were included in this study. Their mean (standard deviation (SD)) age was 53 (8.5) and 77.5 (8) years, respectively. The odds ratios (95% confidence interval, P-value) of some of the pertinent risk factors for mortality for operated adults were 1.04 for time to operation (95%CI: 1.02–1.07, p < 0.001), 2.83 for respiratory diseases (95%CI: 2.02–3.98), and 1.93 for cardiac disease (95%CI: 1.39–2.70), among others. Hospital length of stay was a significant risk factor as well for elderly patients—OR: 1.02 (95%CI: 1.01–1.03, p = 0.002). Conclusions: In adult patients who underwent an operation, time to operation, respiratory diseases, and cardiac disease were some of the main risk factors of mortality. In patients who did not undergo a surgical procedure, malignant neoplasm of the rectosigmoid junction, respiratory disease, and fluid and electrolyte disorders were risk factors of mortality. In this patient group, hospital length of stay was only significant for elderly patients.

1. Introduction

Colorectal cancers are the third most diagnosed cancer in males and the second in females [1,2], and the third leading cause of cancer death in men and women in the United States [3]. Rectal cancer is one of the frequent human malignant neoplasms and the second most common cancer in the large intestine [3]. Differentiation between rectal and sigmoid carcinomas is a diagnostic challenge with important implications for further treatment [4]. All tumors from a 0 to 15 cm distance from the anal verge are usually defined as rectal carcinomas, and all tumors more than 15 cm as sigmoid carcinomas [5]. Rectal carcinomas with positive lymph nodes and/or threatened resection margins on MRI are treated with preoperative therapy, but sigmoid carcinomas are not. Therefore, a correct diagnosis made during the pre-treatment workup is vital [6]. Environmental and genetic factors can affect the likelihood of colon and rectal cancers [7]. Important risk factors of both rectosigmoid junction and rectal cancers are, for example, age, sex, BMI, diet, genetic predisposition, and physical activity. Mortality rate is 30–40% higher in men than in women, though this difference varies by age. Race and ethnicity can also affect the mortality rate; for instance, recent reports from the United States show death rates in Blacks are more than double those in Asians/Pacific Islanders [3]. Studies have shown that patients with rectosigmoid junction neuroendocrine tumors have a better survival and different risk factors than those with rectal neuroendocrine tumors. The treatment choices for rectal neuroendocrine tumors and rectosigmoid junction neuroendocrine tumors may need to be reconsidered [8]. In a study that investigated the effect of treatment delay on cancer-related outcomes in a large, continuous series of surgically treated colon cancer patients, Amri et al. have shown that the delay of treatment was significantly related to the total length of hospital stay, increased morbidity, and mortality [9]. Prolonged time to operation due to the COVID-19 pandemic has shown to be associated with shorter survival times in colorectal cancer [10]. Risk factors for adverse outcomes following emergency surgery for rectal and rectosigmoid neoplasm complications are still debated. The aim of this study was to evaluate the predictors of in-hospital mortality following emergency surgery for complicated rectal and rectosigmoid neoplasms to help identify ways to improve the field and achieve better patient outcomes.

2. Materials and Methods

The National Inpatient Sample (NIS) is a database that is part of the Healthcare Cost and Utilization Project (HCUP), a project sponsored by the Agency for Healthcare Research and Quality (AHRQ). With an annual broad reach of an estimated 7 million patient records, the NIS provides a great degree of power of data analysis across many domains, such as age, sex, clinical characteristics, and geographical location within the United States. The NIS employs the process of weighting when creating the sample of discharges from community hospitals in the US, excluding rehabilitation centers and long-term acute care facilities. This method of stratification allows national estimates of hospitalizations to be made for certain factors. This retrospective cohort study extracted data with the following inclusion criteria: (1) non-elderly adult patients (ages 18–64 years) and elderly patients (65+) (2) with a malignant neoplasm of the rectum or of the rectosigmoid junction (3) who underwent emergency admission from NIS, 2005–2014. The ICD-9 code used to identify patients with a malignant neoplasm of the rectum and rectosigmoid junction was 154. Table 1 contains the ICD-9 codes for surgeries and invasive diagnostic and therapeutic procedure data. The following characteristics of patients and hospitals were collected and analyzed: age, sex, race, income quartile, primary diagnosis, health care insurance (Medicare, Medicaid, private insurance, self-paid, and no charge), hospital location (rural, urban: non-teaching, urban: teaching), neoplasm location (rectosigmoid junction, rectum), invasive diagnostic and/or therapeutic procedure status, surgical procedure status, hospital length of stay, and total charges.

Statistical Analysis

Descriptive statistics were utilized to express categorical variables as numbers, percentages, and ratios. Continuous variables were presented as means and standard deviation. The normality of data was tested through histograms and the Kolmogorov–Smirnov test to make sure that it followed a normal distribution. Given the very large sample size, small departures from normality did not preclude further statistical analysis. Any data that were not normal were examined for outliers to remove from the distribution. If there were no outliers, the data could also undergo a transformation, such as a log or square root to make it normal. Chi square and Student’s t tests were used to compare categorical and continuous variables, respectively. Independent variables were stratified in three ways: (1) according to sex and either adult or elderly, (2) survived patients vs. deceased ones within each age group, and (3) had an operation or did not for both adults and elderly patients. The dependent variable was mortality. The same stratifications were applied to compare the mortality between men and women, deceased vs. survived patients, and operated vs. not-operated patients. Binary multivariable logistic regression analyses with backward elimination were adjusted for the following characteristics of patients and hospitals: age, sex, race, income quartile, health care insurance, hospital location, invasive diagnostic and/or therapeutic procedures, time to operation, and place of tumor (rectum vs. rectosigmoid junction). R Statistical Software (Foundation for Statistical Computing, Vienna, Austria) was used for statistical analysis, and p < 0.05 was set as significant for the analyses.

3. Results

3.1. Sex Differences

3.1.1. Non-Elderly Patients

A total of 4213 (38.6%) patients admitted emergently for rectal or rectosigmoid junction malignant neoplasms were females, and 6705 (61.4%) were males with a similar mean age of about 53 years old. Regardless of the sex, most patients were white, funded mostly by private insurance, and were admitted mostly to a teaching hospital (Table 2). Some major comorbidities among the emergency admitted non-elderly patients were AIDS, alcohol abuse, deficiency anemias, and fluid/electrolyte disorders. Males manifested with significantly higher comorbidities of AIDS, alcohol abuse, drug abuse, liver disease, and renal failure, while females showed higher comorbidities of rheumatoid arthritis, depression, and hypothyroidism. Males underwent more invasive diagnostic and/or therapeutic procedures on the gastrointestinal (GI) system and significantly higher rates of digestive system operations. Patients’ characteristics and clinical data are summarized in Table 2.

3.1.2. Elderly Patients

The mean (SD) age of the females, 79 (8), was significantly higher than the mean (SD) age of the males, 76 (8). Regardless of sex, most patients were white and funded mostly by Medicare (Table 2). Major comorbidities among the emergency admitted elderly patients were hypertension, chronic pulmonary disease, uncomplicated diabetes, renal failure, and fluid/electrolyte disorders, among others. Males manifested significantly higher comorbidities with chronic pulmonary disease, alcohol abuse, peripheral vascular disorders, and renal failure, while females showed higher comorbidities of rheumatoid arthritis, depression, hypothyroidism, obesity, and fluid/electrolyte disorders. Males had less time to surgical procedure. Patients’ characteristics and clinical data are summarized in Table 2.

3.2. Mortality

3.2.1. Adult Patients

A total of 95.5% of patients survived, and 4.5% died within the immediate hospital stay. The mean (SD) age of the patients who survived was 52.81 (8.57) years: 6416 were males (61.6%), and 4003 were females (38.4%), with a similar mean age. The mean (SD) age of the 42 patients who died during the study period was 53.87 (8.05) years: 288 were males (58.18%), and 207 were females (41.82%), with a similar mean age.
When comparing deceased to survived patients, significant differences were noted in terms of certain morbidities. The patients who died manifested significantly higher rates of the following comorbidities: coagulopathy, liver disease, fluid/electrolyte disorders, pulmonary circulation disorders, and renal failure. The adult deceased patients manifested significantly higher rates of rectosigmoid junction malignancies and lower rates of rectal malignancies in comparison to the adult patients that survived. The deceased patients also showed a significantly higher rate of having undergone invasive diagnostic and/or therapeutic procedures on the GI system and a higher rate of undergoing a digestive system operation. Patients’ characteristics and clinical data are summarized in Table 3.

3.2.2. Elderly Patients

A total of 11,933 patients (94.0%) lived and 763 (6%) died within the immediate hospital stay. The patients who survived included 5650 females (47.4%) and 6283 (52.6%) males. The mean (SD) age of the 355 patients who died during the study period was significantly higher in comparison to the patients who survived, 78.55 (8.00) vs. 77.34 (7.92), respectively. When comparing deceased to survived patients, significant differences were noted in terms of morbidities. The deceased patients manifested with significantly higher rates of comorbidities with pulmonary circulation disorders, fluid/electrolyte disorders, coagulopathy, liver disease, and weight loss. The elderly deceased patients had significantly higher rates of rectosigmoid junction and lower rates of rectal malignancies in comparison to the patients that survived. The deceased patients also had a significantly lower rate of undergoing invasive diagnostic and/or therapeutic procedures on the GI system, a lower rate of digestive system operations, and a longer time to invasive and surgical procedures. Patients’ characteristics and clinical data are summarized in Table 3.

3.3. Operation vs. No Operation

3.3.1. Adult Patients

The stratified analysis, based on the surgical procedure status, is presented in Table 4. The mean (SD) age of the patients who had a surgical procedure was significantly higher in comparison to the no surgery group, 53.15 (8.39) years vs. 52.50 (8.74) years, respectively. In both groups, most patients were males. The racial breakdown, by proportion of cases in decreasing order was White, Black, Hispanic, Asian/Pacific Islander, and Native American. Most patients were funded mostly by private insurance and were admitted to urban teaching hospitals. In the group that had a surgical procedure, the rate of comorbidities, such as metastatic cancer and solid tumors, was significantly higher in comparison to the other group. They furthermore manifested with a higher rate of rectosigmoid junction neoplasm and of rectal neoplasm, a higher rate of invasive diagnostic and/or therapeutic procedures on GI, a longer time to invasive diagnostic and/or therapeutic procedure, a longer hospital length of stay (HLOS), and a lower mortality. Patients’ characteristics and clinical data are summarized in Table 4. In total, 44.3% of the surgical procedures on adult patients with this diagnosis were operations on the intestines (ICD-9 codes 45.00–45.03, 45.30–46.99), which included excisions and colostomies. Similarly, 42.8% of the invasive diagnostic and/or therapeutic procedures were performed on the intestines (ICD-9 codes 45.11–45.29).

3.3.2. Elderly Patients

The stratified analysis, based on the surgical procedure status, is also presented in Table 4. Out of 12,701 emergency admitted elderly patients with the primary diagnosis of malignant neoplasm of the rectum and rectosigmoid junction, 7238 (57.0%) had a surgical procedure. The mean (SD) age of the patients who went through a surgical procedure was significantly lower in comparison to the no surgery group, 76.90 (8.39) years vs. 78.09 (8.19) years, respectively. In both groups, most patients were males. The racial breakdown by proportion of cases in decreasing order was White, Black, Hispanic, Asian/Pacific Islander, and Native American. Most patients were funded mostly by Medicare and were admitted to urban teaching hospitals. In the group that had a surgical procedure, the rate of comorbidities, such as metastatic cancer, solid tumors, hypertension, and fluid/electrolyte disorders, was significantly higher in comparison to the other group. They furthermore manifested a higher rate of rectosigmoid junction rectal neoplasm, a higher rate of invasive diagnostic and/or therapeutic procedures on the GI system, a longer HLOS, and significantly lower mortality rates. Patients’ characteristics and clinical data are summarized in Table 4. For elderly patients, 42.5% of the surgical procedures and 47.6% of the invasive diagnostic and/or therapeutic procedures were conducted on the intestine.

3.4. Risk Factors of Mortality

The multivariable logistic regression model with backward elimination for mortality was built for the patients that underwent an operation and compared with the model built for the group that did not undergo an operation. The findings are presented in Table 5 and Table 6. Common variables included were age, sex, comorbidities, social factors, lifestyle, and invasive diagnostic and/or therapeutic procedures. Time to surgery was added to the regression model built for patients with operation. HLOS was added to the model built for the group with no operation.

3.4.1. Operated Adult Patients

Table 5 compares mortality in adults and elderly patients that underwent an operation. For adult patients, one day of increased time to operation increased the odds of mortality by 4%. Undergoing invasive diagnostic and/or therapeutic procedures reduced the odds of mortality by 51%. Bacterial infections increased the mortality odds by 2.94-fold. Respiratory diseases similarly elevated the odds by 2.83 times. Patients with a coagulopathy had higher odds of dying by 58%, while those with cardiac disease experienced a 93% increase. Additional risk factors were fluid and electrolyte disorders, liver disease, and neoplasms.

3.4.2. Operated Elderly Patients

Similar risk factors of mortality for both elderly and adult patients included age, time to operation, bacterial infections other than tuberculosis, respiratory diseases, coagulopathy, and fluid and electrolyte disorders. For every additional year of age, patients demonstrated higher mortality odds of 3%. Each day of delay to surgery elevated the odds of death by 5%. Being female offered a protective mortality benefit of 22%. Respiratory infections increased the odds of mortality by 2.61-fold. Patients with a coagulopathy manifested a 48% increase in odds of mortality.

3.4.3. Non-Operated Adult Patients

Table 6 compares the mortality between non-operated adults and elderly patients. Undergoing an invasive diagnostic and/or therapeutic procedure provided an 87% protective mortality benefit for these patients. For liver diseases, patients demonstrated a 95% increase in mortality odds. Having a malignant neoplasm of the rectosigmoid junction, as opposed to that of the rectum, manifested 36% higher odds of mortality. Respiratory diseases elevated the mortality odds by 2.06-fold, while liver disease increased it by 1.95-fold. Other risk factors included fluid and electrolyte disorders, neoplasms, coagulopathy, neurological diseases, skin disease and trauma, burns, and poisons. HLOS was not a risk factor of mortality in these patients.

3.4.4. Non-Operated Elderly Patients

Common risk factors of elderly and adult patients who had no operation were having a malignant neoplasm of the rectosigmoid joint, respiratory disease, and fluid and electrolyte disorders. In the elderly group, each additional year of age raised the mortality risk by 1%. Those that underwent invasive diagnostic and/or therapeutic procedures demonstrated an 81% decrease in mortality odds. Patients with a cancerous lesion of the rectosigmoid junction, as opposed to the rectum had 51% higher odds of dying. For each additional day in the hospital, their mortality risk increased by 2%.

3.5. Possible Causes of Mortality

Supplementary Table S1 summarizes the secondary diagnoses in adult and elderly patients, comparing those that survived vs. those that passed away in the immediate hospital stay. For both adult and elderly patients, some of the pertinent possible causes of death included bacterial infections not including tuberculosis, diabetes, hypertension, coagulopathy, and cardiac disease.

3.5.1. Adult Patients

The possible causes of death in this patient population included nonbacterial infections, diabetes or chronic diabetes complications, anemia and/or hemorrhage, respiratory diseases, and skin diseases, among many others (Supplementary Table S1).

3.5.2. Elderly Patients

Some of the possible causes of death in this population included liver disease, disease of the digestive tract, neurological disease, diseases of the musculoskeletal system, tobacco use, platelet and white blood cell disorders, and many others (Supplementary Table S1).

4. Discussion

The primary aim of this study was to evaluate associations between demographics, socioeconomic status, comorbidities, time to operation, surgical procedure status, postoperative HLOS, and mortality in emergency patients with primary diagnosis of malignant neoplasm of the rectum and rectosigmoid junction. Emergent colorectal procedures are associated with significant morbidity and mortality [11]. Risk factors for adverse outcomes following emergency surgery for colon cancer complications are still debated. Our results demonstrated that in emergency admitted patients with the primary diagnosis of malignant neoplasm of the rectum and rectosigmoid junction, time to surgery, hospital length of stay, age, place of malignancy, and several comorbidities were the main risk factors of mortality, whereas invasive diagnostic and/or therapeutic procedures served as a protective factor. Some factors were repeatedly found to be the predictors of mortality, including emergency surgery, age, patient health status [12,13], grade of the malignant tumor, number and location of metastases, and resection margin [14].

4.1. The Impact of HLOS on the Mortality Risk

Our analysis showed in Table 6 that in elderly patients that did not undergo an operation, each additional day in the hospital increased the odds of mortality by 2%. In support of our results, Van Vliet et al. have shown that as HLOS has become significantly shorter for more patients, older patients are less often exposed to the hazards of longer hospital admissions, such as decline in mobility, activities in daily living, and mortality [15]. Better functional outcomes and lower mortality are associated with short admissions, which suggests an advantage of the decrease in HLOS. Enhanced recovery after surgery programs (ERAS) have been introduced with aims of improving patient care, reducing complication rates, and shortening hospital stay following colorectal surgery [16,17]. ERAS have been shown to sustain their effects on emergency surgery patients as well [18,19] with no impact on reducing mortality rates [20,21,22]. A valuable study to analyze the impact of ERAS on HLOS for emergency surgery cases should aim to test the model of Balvardi et al. and compare the patient and hospital characteristics that are associated with discrepancies between HLOS and “time-to-readiness for discharge” measures, as emergency surgery is not included in their study [23]. The crucial role of preoperative assessment, which is omitted in emergency cases and therefore shortens HLOS, including obtaining the necessary clearances and anesthesia evaluation, is well-established [24]. An inability to move the patient to a stable preoperative course, by preventing the preoperative assessment, can be a factor contributing to an increased mortality risk as well, as it could have importance in terms of an underlying propensity for decompensation.

4.2. The Impact of Delay in Operation on the Mortality Risk

Our results demonstrated in Table 5 that in emergently admitted patients with the primary diagnosis of a malignant neoplasm of the rectum or rectosigmoid junction that have undergone an operation, time to surgery was among the main risk factors of mortality. Each day delay to the first surgery elevated the odds of mortality by 4% in adult and 5% in elderly patients. Minimizing the delay to definitive operative care may improve outcomes [25]. At present, there are insufficient data regarding the impact of delay in emergency operation and prolonged stay in the hospital on the mortality of emergency admitted patients with the primary diagnosis of malignant neoplasm of the rectum and rectosigmoid junction. Grass et al. assessed the impact of delay from diagnosis to curative surgery on survival in patients with non-metastatic colon cancer and observed that the adjusted hazard ratio for mortality increased with delay times of longer than 30 days, to become significant after a delay of 40 days [26]. In prior NIS database studies, emergently admitted patients with ventral hernia, chronic duodenal ulcers, or hemorrhoids with previous surgery exhibited longer time to operation among the main risk factors for mortality [27,28,29,30].

4.3. The Impact of Age on the Mortality Risk

Our findings demonstrated that age was a risk factor of mortality in elderly patients regardless of operation status. Overall, the mortality rate was 4.5% in adult and 6% in elderly patients in the current study, and for every one year that the elderly patient became older, the odds of mortality increased by 1–3%. In the general population, healthy adults from the ages of 18 to 64 have an additional chance of death ranging from 0.02% to 0.3% per year as they grow older. It has previously been shown that young to middle-aged adults have a better overall survival of colorectal cancer as compared to both patients over sixty-five and patients under twenty-one [31]. This difference in survival might partly be explained by the burden of more advanced stage cancers in younger patients and higher postoperative complication risks in older adults because of comorbidities. Although age could be a major player in the algorithm for determining the appropriateness of surgery, the emergency nature of these procedures combined with a poor response to alternative treatments makes surgery an often-imperative risk to take. This finding suggests an opportunity for patient care optimization in patients undergoing emergency surgery for the complications of colon cancer.
A mortality rate at least two to three times higher among the elderly than among younger patients has been repeatedly reported in various populations [32]. In the Netherlands, advanced age and acute operation are by far the most important factors related to operative mortality after colorectal resection [33,34].

4.4. The Impact of Sex on the Mortality Risk

The current study showed that being of the female sex is a risk factor in elderly patients that do not undergo an operation but is protective in elderly patients that do undergo an operation. The impact of sex on colorectal cancer incidence is well established. In support of our results, previous studies showed that at all ages, women are less likely to develop colorectal cancers than men [35,36]. In the Women’s Health Initiative trial, post-menopausal estrogen and progestin use was associated with a 40% decrease in colorectal cancer, indicating a role in colorectal cancer carcinogenesis and tumor progression [37]. These hormones are found to also protect pre-menopausal women, as oral contraceptive use reduces the risk of developing colorectal cancers by approximately 20% [38]. We demonstrated that female sex is a predictor for improved survival, and as supported by several studies, male sex adversely affects survival following surgery for colorectal cancer [39,40].
Siegal et al. demonstrated that mortality rate is 30–40% higher in men than in women, although this difference varies by age [3]. A sedentary lifestyle and associated obesity further increase the risk of colon cancer mostly in men [41,42]. Interestingly, and in contrast to previous studies [43,44], our results demonstrate that females sustain their advantage at all ages until 85+, which suggests that the estrogen-related protection is not the only factor associated with their survival.

4.5. Rectal vs. Rectosigmoid Malignancy

We have shown in Table 6 that the patients with rectosigmoid junction cancer had 36 and 51 percent higher rates of mortality than those with rectal cancer in adult and elderly patients, respectively. The International Classification of Diseases has recognized the rectosigmoid junction as a unique element and a transition zone separating the sigmoid colon and rectum for further diversification in management and outcomes [45]. The American Joint Committee on Cancer (AJCC) staging system and the Surveillance, Epidemiology, and End Results Program (SEER) database have also recognized the rectosigmoid as a distinct segment; however, currently, cancer of the rectosigmoid junction is still being treated as colon cancer. Previous studies have shown a poor outcome of cancers of the rectosigmoid segment [46,47], which are believed to be associated with different patterns of lymphatic spread with earlier or more frequent metastases to pararectal nodes [48] and therefore likely appear more advanced in presentation. It might be that a wrong-site allocation by endoscopic or radiological test results in the miscoding of upper rectal or distal sigmoid as rectosigmoid cancers [49]. Since the therapeutic options are significantly different when addressing malignancies of the rectum and rectosigmoid, there is an effort to form a consistent definition and to reach a consensus [50,51]. Additional analysis is required to discover the key cause of these fundamental differences between the rectum and the rectosigmoid malignancy.

4.6. Surgical Status

Our results in Table 5 and Table 6 showed that the impact of the surgery status on mortality rate was multifactorial and inclusive. In support, the scientific community did not achieve consensus as well. Antony et al. have concluded after risk adjustment that urgent surgery in colon cancer has no impact on survival [52]. On the other hand, Ramos et al. claimed that there was a high mortality rate and a low survival rate in colorectal cancer patients operated on urgently [53]. Smothers et al. claimed that emergency surgery has a strong negative influence on immediate surgical morbidity and mortality; however, other coexistent factors, such as advanced disease, the age of the patient, and medical comorbid conditions, may also influence these outcomes [54]. Goldstone et al. added that operative approach and surgeon training have a substantial impact on outcomes following urgent/emergent colon surgery [55]. Postoperative mortality was two-fold greater when non-colorectal surgeons performed primary anastomosis vs. the Hartmann procedure. Further research is required to evaluate the impact of neoplasm characteristics, timing, and surgical approach on mortality.

4.7. Comorbidities and Possible Causes of Death

As expected, comorbid conditions had a great impact on postoperative outcomes and possible mortality, as seen in Table 5 and Table 6 and Supplementary Table S1. Common comorbidities between both adult and elderly patients shown as risk factors included coagulopathy, hypertension, liver disease, fluid/electrolyte disorders, metastatic cancer, and pulmonary circulation disorders, among others. In support of our results, studies showed that in patients undergoing colorectal surgery, emergent surgery, liver disease, total colectomy, age older than 65 years, chronic renal failure, and malignant tumor were the major risk factors for in-hospital mortality [56]. Coagulopathy, pulmonary circulatory disorders, liver disorders, renal failure, fluid and electrolyte abnormalities, solid tumors, metastasis, weight loss, AIDS, and alcohol abuse were found to be associated with increased mortality rates. Such mortality rates in patients with coagulopathy may be explained by the increased risk and severity of malignant neoplasm of the rectum and rectosigmoid junction cancer bleeding [57,58]. Moreover, coagulopathies add to the perioperative risk in case surgical hemostasis is indicated [59]. The significantly increased mortality seen in patients with fluid/electrolyte disorders, as presented in Table 5 and Table 6 and Supplementary Table S1, is consistent with previous studies, which have highlighted the significant prevalence of hyponatremia in patients with colorectal cancer and the severity-dependent increase in mortality in these patients [60,61]. Hypernatremia was found to be a comorbid condition that was strongly predictive of perioperative death [62]. Congestive heart failure is intimately associated with electrolyte balance, perfusion status, and overall robustness to the trauma of both the malignancy as well as the surgical intervention. Therefore, it has been associated with increased rates of surgical complications and death [62].

4.8. The Impact of Invasive Diagnostic and Therapeutic Procedures on Mortality

Our study shows that an invasive diagnostic served as a protective factor in Table 5 and Table 6. In support of these data, Lasisi and Rex have shown improved protection against proximal colon cancer by cecal intubation in screening examinations [62]. Additional studies proved that colonoscopy was strongly associated with reduced odds of both distal and proximal colorectal cancer [63], offered onco-protective effects in both the left and right colon, and confirmed the positive impact on survival in both locations [64]. Colonoscopy was found to be the most effective strategy for detection of precancerous lesions, including large conventional adenomas and large serrated lesions [65]. These findings confirm the need for the continued improvement of invasive diagnostic and therapeutic procedures, their effectiveness, and obligatory quality assessment to optimize the diagnostic yield and its protective factor.

4.9. Strengths of the Study

The combination approach of the logistic regression model and the thorough NIS database was the main strength of the current study. This database contains data of patients from multiple states and includes health-based, administrative, and population-based data in a uniform format. The purpose of these data is to improve healthcare through research by analyzing broad combinations of disease conditions, treatments, and outcomes in a large sample size over a ten-year span. Previous studies in the literature focused on smaller subsets of the population over a smaller geographical location in a shorter period of time. This study serves to fill a part of the gap in the literature on the demographics of adult and elderly patients suffering from a rectal or rectosigmoid malignancy as well as their individual hospital course, disease management, and the eventual result of their care.

4.10. Limitations of the Study

As with any retrospective cohort analysis, there is a level of inherent limitation to the data; hence, it is important to interpret the data with that in mind. Due to the fact that it is a retrospective study using an administrative dataset, there are variables that cannot be obtained, which would greatly help to further contextualize the results. Given that the principal goal of the study was to identify factors that influence in-hospital mortality in emergency surgery of colon cancer, it would be very helpful to add an additional element of analysis of the causes of death among patients to stratify the associations noted by cause. Another such contextualizing aspect that is missing, given the analysis of patient disposition, is an assessment of functional ability prior to emergency surgery, which would be beneficial. By identifying the level of care required by the patient, such as home health or skilled nursing facility, there would be a more nuanced understanding of whether the disposition is a return to the status quo or an escalation in care status needed by the patient. Additionally, given that comorbidities were among the most influential factors that increased mortality in both associations, it would be helpful to have an understanding of how multiple comorbidities can potentially interact, or simply co-exist, to influence survival following the trauma of abdominal surgery, due to synergistic effects on physical stress. Along those lines, there is potential for a circular influence of the predictors of mortality on outcome. For example, the hospital length of stay can predict the risk of mortality. However, the stay in the hospital will be shorter if the patient dies. Similarly, if a patient undergoes an emergency surgery, that in itself signifies a worse prognosis. Another potential limitation is that the use of a backwards elimination without validation on a separate dataset can potentially overestimate any associations.
The lack of consensus over the transition point for the end of the sigmoid and beginning of the rectum is a problem for the colorectal multidisciplinary team and could have impacted our results [46]. Without a reliable definition of the rectum, rectosigmoid and rectal cancers will be classified inconsistently. As the treatment strategies for rectosigmoid and rectal cancers are radically different, incorrect tumor localization has a substantial impact on patient management, leading to under or over treatment [66]. If a rectal tumor is misclassified as a rectosigmoid tumor, the patient could be inadequately staged and not considered for preoperative downstaging radiation, potentially decreasing their chance of undergoing a complete resection and worsening their survival [67]. Although this is a situational clinical limitation, it could have had a distorting impact on our results. An additional limitation of this study is a lack of the specification of the tumor origin and size, shape of the tumor, perforation and obstruction status, degree of differentiation, proper staging and localization using CT/MRI [68,69] and venous invasion, number of metastases, relevant GI neoplasm family history, operative approach and surgeon training, and whether the diagnosis was made using radiological markings, endoscopic measurements, or anatomical landmarks [70,71]. Further research on the complexity of cases and other modifiable patient factors that could influence patient discharge is necessary.

5. Conclusions

In conclusion, an increased time to first surgical procedure, bacterial infections, coagulopathy, cardiac disease, and respiratory disease are risk factors for in-hospital mortality in both adult and elderly patients undergoing emergency surgery for malignant neoplasm of the rectum and rectosigmoid junction, among others. Malignant neoplasm of the rectosigmoid junction as opposed to the rectum or other neoplasms, fluid and electrolyte disorders, and respiratory disease were risk factors, among others, for in-hospital mortality in adult and elderly patients that did not undergo an operation. Liver disease, coagulopathy, and cardiac disease were risk factors for mortality in non-operated adult patients, while age, hospital length of stay, and female sex were risk factors for non-operated elderly patients.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/ijerph19159203/s1, Supplementary Table S1: Secondary diagnoses of patients emergently admitted with a primary diagnosis of malignant neoplasm of rectum or rectosigmoid junction (NIS 2004–2014). Data was stratified according to survival status.

Author Contributions

Conceptualization, A.S. and R.L.; methodology, A.S. and R.L.; software, A.S.; validation, A.S. and R.L.; formal analysis, A.S.; investigation, L.L.; resources, R.L.; data curation, A.S.; writing—original draft preparation, L.L.; writing—review and editing, A.S. and R.L.; visualization, A.S. and L.L.; supervision, A.S. and R.L.; project administration, R.L.; funding acquisition, not applicable. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

The study was conducted in accordance with the Declaration of Helsinki and approved by the Institutional Review Board of New York Medical College (protocol code 14177 approved in June 2019).

Informed Consent Statement

Not applicable.

Data Availability Statement

Data will be available for verification purposes upon request.

Acknowledgments

We thank Jonathan Butler for his help in statistical analysis.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Fleming, M.; Ravula, S.; Tatishchev, S.F.; Wang, H.L. Colorectal carcinoma: Pathologic aspects. J. Gastrointest. Oncol. 2012, 3, 153–173. [Google Scholar] [CrossRef]
  2. Global Burden of Disease Cancer Collaboration; Fitzmaurice, C.; Allen, C.; Barber, R.M.; Barregard, L.; Bhutta, Z.A.; Brenner, H.; Dicker, D.J.; Chimed-Orchir, O.; Dandona, R.; et al. Global, Regional, and National Cancer Incidence, Mortality, Years of Life Lost, Years Lived With Disability, and Disability-Adjusted Life-years for 32 Cancer Groups, 1990 to 2015: A Systematic Analysis for the Global Burden of Disease Study. JAMA Oncol. 2017, 3, 524–548. [Google Scholar] [CrossRef]
  3. Siegel, R.; Desantis, C.; Jemal, A. Colorectal cancer statistics, 2014. CA Cancer J. Clin. 2014, 64, 104–117. [Google Scholar] [CrossRef]
  4. Moltzer, E.; Noordman, B.J.; Renken, N.S.; Roos, D. Determination of Tumor Location in Rectosigmoid Carcinomas: Difficulties in Preoperative Diagnostics. Gastrointest. Disord. 2019, 1, 210–219. [Google Scholar] [CrossRef] [Green Version]
  5. Glynne-Jones, R.; Wyrwicz, L.; Tiret, E.; Brown, G.; Rödel, C.; Cervantes, A.; Arnold, D. Rectal cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment, and follow-up. Ann. Oncol. 2017, 28 (Suppl. 4), iv22–iv40. [Google Scholar] [CrossRef] [PubMed]
  6. Salibasic, M.; Pusina, S.; Bicakcic, E.; Pasic, A.; Gavric, I.; Kulovic, E.; Rovcanin, A.; Beslija, S. Colorectal Cancer Surgical Treatment, our Experience. Med. Arch. 2019, 73, 412–414. [Google Scholar] [CrossRef]
  7. Wei, E.K.; Giovannucci, E.; Wu, K.; Rosner, B.; Fuchs, C.S.; Willett, W.C.; Colditz, G. Comparison of risk factors for colon and rectal cancer. Int. J. Cancer 2004, 108, 433–442. [Google Scholar] [CrossRef] [Green Version]
  8. Cai, W.; Ge, W.; Hu, H.; Mao, J. Rectal NETs and rectosigmoid junction NETs may need to be treated differently. Cancer Med. 2019, 9, 971–979. [Google Scholar] [CrossRef]
  9. Amri, R.; Bordeianou, L.; Sylla, P.; Berger, D. Treatment Delay in Surgically Treated Colon Cancer: Does It Affect Outcomes? Ann. Surg. Oncol. 2014, 21, 3909–3916. [Google Scholar] [CrossRef]
  10. Dillard, R. Surgical Delays Due to COVID-19 Are Associated with Shorter Survival Times in Patients with Colorectal Cancer. Docwire News. 8 July 2020. Available online: https://www.docwirenews.com/docwire-pick/hem-onc-picks/surgical-delays-due-to-covid-19-are-associated-with-shorter-survival-times-in-patients-with-colorectal-cancer/ (accessed on 26 April 2021).
  11. Yilmaz, Y.; Cengiz, F.; Kamer, E.; Acar, T.; Gür, E.; Bag, H.; Peker, Y.; Atahan, K. The factors that affect the mortality of emergency operated ASA 3 colon cancer patients. Pan Afr. Med. J. 2020, 36, 290. [Google Scholar] [CrossRef]
  12. Pisano, M.; Zorcolo, L.; Merli, C.; Cimbanassi, S.; Poiasina, E.; Ceresoli, M.; Agresta, F.; Allievi, N.; Bellanova, G.; Coccolini, F.; et al. 2017 WSES guidelines on colon and rectal cancer emergencies: Obstruction and perforation. World J. Emerg. Surg. 2018, 13, 36. [Google Scholar] [CrossRef] [PubMed]
  13. Weixler, B.; Warschkow, R.; Güller, U.; Zettl, A.; Von Holzen, U.; Schmied, B.M.; Zuber, M. Isolated tumor cells in stage I & II colon cancer patients are associated with significantly worse disease-free and overall survival. BMC Cancer 2016, 16, 106. [Google Scholar] [CrossRef] [Green Version]
  14. Fujita, S.; Akasu, T.; Moriya, Y. Resection of synchronous liver metastases from colorectal cancer. Jpn. J. Clin. Oncol. 2000, 30, 7–11. [Google Scholar] [CrossRef]
  15. Vliet, M.; van Huisman, M.; Deeg, D.J.H. Decreasing Hospital Length of Stay: Effects on Daily Functioning in Older Adults. J. Am. Geriatr. Soc. 2017, 65, 1214–1221. [Google Scholar] [CrossRef] [Green Version]
  16. Rawlinson, A.; Kang, P.; Evans, J.; Khanna, A. A systematic review of enhanced recovery protocols in colorectal surgery. Ann. R. Coll. Surg. Engl. 2011, 93, 583–588. [Google Scholar] [CrossRef] [Green Version]
  17. Ljungqvist, O.; Scott, M.; Fearon, K.C. Enhanced Recovery After Surgery: A Review. JAMA Surg. 2017, 152, 292. [Google Scholar] [CrossRef] [PubMed]
  18. Roulin, D.; Blanc, C.; Muradbegovic, M.; Hahnloser, D.; Demartines, N.; Hübner, M. Enhanced recovery pathway for urgent colectomy. World J. Surg. 2014, 38, 2153–2159. [Google Scholar] [CrossRef]
  19. Wisely, J.C.; Barclay, K.L. Effects of an Enhanced Recovery After Surgery programme on emergency surgical patients. ANZ J. Surg. 2016, 86, 883–888. [Google Scholar] [CrossRef]
  20. Paduraru, M.; Ponchietti, L.; Casas, I.M.; Svenningsen, P.; Zago, M. Enhanced Recovery after Emergency Surgery: A Systematic Review. Bull. Emerg. Trauma 2017, 5, 70–78. [Google Scholar] [PubMed]
  21. Gonenc, M.; Dural, A.C.; Celik, F.; Akarsu, C.; Kocatas, A.; Kalayci, M.U.; Dogan, Y.; Alis, H. Enhanced postoperative recovery pathways in emergency surgery: A randomised controlled clinical trial. Am. J. Surg. 2014, 207, 807–814. [Google Scholar] [CrossRef]
  22. Lohsiriwat, V. Enhanced recovery after surgery vs. conventional care in emergency colorectal surgery. World J. Gastroenterol. 2014, 20, 13950–13955. [Google Scholar] [CrossRef] [PubMed]
  23. Balvardi, S.; Pecorelli, N.; Castelino, T.; Niculiseanu, P.; Liberman, A.S.; Charlebois, P.; Stein, B.; Carli, F.; Mayo, N.E.; Feldman, L.S.; et al. Measuring In-Hospital Recovery After Colorectal Surgery Within a Well-Established Enhanced Recovery Pathway: A Comparison Between Hospital Length of Stay and Time to Readiness for Discharge. Dis. Colon Rectum 2018, 61, 854–860. [Google Scholar] [CrossRef] [PubMed]
  24. Arnold, M.J.; Beer, J. Preoperative evaluation: A time-saving algorithm. J. Fam. Pract. 2016, 65, 706–710. [Google Scholar]
  25. McGillicuddy, E.A. Factors Predicting Morbidity and Mortality in Emergency Colorectal Procedures in Elderly Patients. Arch. Surg. 2009, 144, 1157. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  26. Grass, F.; Behm, K.T.; Duchalais, E.; Crippa, J.; Spears, G.M.; Harmsen, W.S.; Hübner, M.; Mathis, K.L.; Kelley, S.R.; Pemberton, J.H.; et al. Impact of delay to surgery on survival in stage I–III colon cancer. Eur. J. Surg. Oncol. 2020, 46, 455–461. [Google Scholar] [CrossRef]
  27. Smiley, A.; Levy, L.; Latifi, R. Risk Factors for Mortality in Patients with Ventral Hernia Admitted Emergently: An Analysis of 48,539 Adult Patients. Surg. Technol. Int. 2021, 39, 1497. [Google Scholar] [CrossRef]
  28. Latifi, R.; Levy, L.; Reddy, M.; Okumura, K.; Smiley, A. Delayed Operation as a Major Risk Factor for Mortality among Elderly Patients with Ventral Hernia Admitted Emergently: An Analysis of 33,700 Elderly Patients. Surg. Technol. Int. 2021, 39, 1520. [Google Scholar] [CrossRef]
  29. Levy, L.; Smiley, A.; Latifi, R. Independent Predictors of In-Hospital Mortality in Elderly and Non-Elderly Adult Patients Undergoing Emergency Admission for Hemorrhoids in the USA: A 10-Year National Dataset. Am. Surg. 2022, 88, 936–942. [Google Scholar] [CrossRef]
  30. Lin, N.; Smiley, A.; Goud, M.; Lin, C.; Latifi, R. Risk Factors of Mortality in Patients Hospitalized with Chronic Duodenal Ulcers. Am. Surg. 2022, 88, 764–769. [Google Scholar] [CrossRef] [PubMed]
  31. Poles, G.; Clark, D.; Mayo, S.W. Colorectal carcinoma in pediatric patients: A comparison with adult tumors, treatment, and outcomes from the National Cancer Database. J. Pediatric Surg. 2016, 51, 1061–1066. [Google Scholar] [CrossRef]
  32. Manceau, G.; Mege, D.; Bridoux, V.; Lakkis, Z.; Venara, A.; Voron, T.; Sielezneff, I.; Karoui, M. Emergency Surgery for Obstructive Colon Cancer in Elderly Patients: Results of a Multicentric Cohort of the French National Surgical Association. Dis. Colon Rectum 2019, 62, 941–951. [Google Scholar] [CrossRef] [PubMed]
  33. Engel, A.F.; Oomen, J.L.T.; Knol, D.L.; Cuesta, M.A. Operative mortality after colorectal resection in the Netherlands. Br. J. Surg. 2005, 92, 1526–1532. [Google Scholar] [CrossRef] [PubMed]
  34. Endreseth, B.H.; Romundstad, P.; Myrvold, H.E.; Bjerkeset, T.; Wibe, A. Rectal cancer treatment of the elderly. Colorectal Dis. 2006, 8, 471–479. [Google Scholar] [CrossRef] [PubMed]
  35. Nelson, R.L.; Dollear, T.; Freels, S.; Persky, V. The relation of age, race, and gender to the subsite location of colorectal carcinoma. Cancer 1997, 80, 193–197. [Google Scholar] [CrossRef]
  36. Farquhar, C.M.; Marjoribanks, J.; Lethaby, A.; Lamberts, Q.; Suckling, J.A.; Cochrane HT Study Group. Long term hormone therapy for perimenopausal and postmenopausal women. Cochrane Database Syst. Rev. 2017, 1, CD004143. [Google Scholar] [CrossRef]
  37. Chlebowski, R.T.; Wactawski-Wende, J.; Ritenbaugh, C.; Hubbell, F.A.; Ascensao, J.; Rodabough, R.J.; Rosenberg, C.A.; Taylor, V.M.; Harris, R.; Chen, C.; et al. Estrogen plus progestin and colorectal cancer in postmenopausal women. N. Engl. J. Med. 2004, 350, 991–1004. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  38. Hannaford, P.C.; Selvaraj, S.; Elliott, A.M.; Angus, V.; Iversen, L.; Lee, A.J. Cancer risk among users of oral contraceptives: Cohort data from the Royal College of General Practitioner’s oral contraception study. BMJ 2007, 335, 651. [Google Scholar] [CrossRef] [Green Version]
  39. Wichmann, M.W.; Müller, C.; Hornung, H.M.; Lau-Werner, U.; Schildberg, F.W.; Colorectal Cancer Study Group. Gender differences in long-term survival of patients with colorectal cancer. Br. J. Surg. 2001, 88, 1092–1098. [Google Scholar] [CrossRef]
  40. McArdle, C.S.; McMillan, D.C.; Hole, D.J. Male gender adversely affects survival following surgery for colorectal cancer. Br. J. Surg. 2003, 90, 711–715. [Google Scholar] [CrossRef]
  41. Giovannucci, E.; Ascherio, A.; Rimm, E.B.; Colditz, G.A.; Stampfer, M.J.; Willett, W.C. Physical activity, obesity, and risk for colon cancer and adenoma in men. Ann. Intern. Med. 1995, 122, 327–334. [Google Scholar] [CrossRef] [PubMed]
  42. Howard, R.A.; Freedman, D.M.; Park, Y.; Hollenbeck, A.; Schatzkin, A.; Leitzmann, M.F. Physical activity, sedentary behavior, and the risk of colon and rectal cancer in the NIH-AARP Diet and Health Study. Cancer Causes Control 2008, 19, 939–953. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  43. Koo, J.H.; Jalaludin, B.; Wong, S.K.C.; Kneebone, A.; Connor, S.J.; Leong, R.W.L. Improved survival in young women with colorectal cancer. Am. J. Gastroenterol. 2008, 103, 1488–1495. [Google Scholar] [CrossRef] [PubMed]
  44. Hendifar, A.; Yang, D.; Lenz, F.; Lurje, G.; Pohl, A.; Lenz, C.; Ning, Y.; Zhang, W.; Lenz, H.-J. Gender Disparities in Metastatic Colorectal Cancer Survival. Clin. Cancer Res. 2009, 15, 6391–6397. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  45. Carroll, N.M.; Ritzwoller, D.P.; Banegas, M.P.; O’Keeffe-Rosetti, M.; Cronin, A.M.; Uno, H.; Hornbrook, M.C.; Hassett, M.J. Performance of Cancer Recurrence Algorithms After Coding Scheme Switch from International Classification of Diseases 9th Revision to International Classification of Diseases 10th Revision. JCO Clin. Cancer Inform. 2019, 3, 1–9. [Google Scholar] [CrossRef] [PubMed]
  46. Falch, C.; Mueller, S.; Braun, M.; Gani, C.; Fend, F.; Koenigsrainer, A.; Kirschniak, A. Oncological outcome of carcinomas in the rectosigmoid junction compared to the upper rectum or sigmoid colon—A retrospective cohort study. Eur. J. Surg. Oncol. 2019, 45, 2037–2044. [Google Scholar] [CrossRef] [PubMed]
  47. Bussotti, C.; Burattini, M.F.; Ricci, E.; Giuliani, N.; Bufalari, A.; Servoli, A.; Rulli, A.; Cavazzoni, E.; Moriconi, E.; Barberini, F. Rectosigmoid junction neoplasms: Our experience. G. Chir. 2003, 24, 409–412. [Google Scholar]
  48. Park, I.J.; Choi, G.S.; Lim, K.H.; Kang, B.M.; Jun, S.H. Different Patterns of Lymphatic Spread of Sigmoid, Rectosigmoid, and Rectal Cancers. Ann. Surg. Oncol. 2008, 15, 3478. [Google Scholar] [CrossRef]
  49. Loffeld, R.J.L.F.; Flens, M.; Fransen, G.; den Boer, F.C.; van Bochove, A. The localisation of cancer in the sigmoid, rectum or rectosigmoid junction using endoscopy or radiology-What is the most accurate method? J. Gastrointest. Oncol. 2014, 5, 469–473. [Google Scholar] [CrossRef]
  50. Sauer, R.; Becker, H.; Hohenberger, W.; Rodel, C.; Wittekind, C.; Fietkau, R.; Martus, P.; Tschmelitsch, J.; Hager, E.; Hess, C.F.; et al. Preoperative versus postoperative chemoradiotherapy for rectal cancer. N. Engl. J. Med. 2004, 351, 1731–1740. [Google Scholar] [CrossRef] [Green Version]
  51. Hofheinz, R.D.; Wenz, F.; Post, S.; Matzdorff, A.; Laechelt, S.; Hartmann, J.T.; Müller, L.; Link, H.; Moehler, M.; Kettner, E.; et al. Chemoradiotherapy with capecitabine versus fluorouracil for locally advanced rectal cancer: A randomised, multicentre, non-inferiority, phase 3 trial. Lancet Oncol. 2012, 13, 579–588. [Google Scholar] [CrossRef]
  52. Antony, P.; Harnoss, J.C.; Warschkow, R.; Schmied, B.M.; Schneider, M.; Tarantino, I.; Ulrich, A. Urgent surgery in colon cancer has no impact on survival. J. Surg. Oncol. 2019, 119, 1170–1178. [Google Scholar] [CrossRef] [PubMed]
  53. Ramos, R.F.; Dos-Reis, L.C.S.; Teixeira, B.E.B.; Andrade, I.M.; Sulzbach, J.S.; Leal, R.A. Colon cancer surgery in patients operated on an emergency basis. Rev. Col. Bras. Cir. 2017, 44, 465–470. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  54. Smothers, L.; Hynan, L.; Fleming, J.; Turnage, R.; Simmang, C.; Anthony, T. Emergency surgery for colon carcinoma. Dis. Colon Rectum 2003, 46, 24–30. [Google Scholar] [CrossRef] [PubMed]
  55. Goldstone, R.N.; Cauley, C.E.; Chang, D.C.; Kunitake, H.; Ricciardi, R.; Bordeianou, L. The Effect of Surgical Training and Operative Approach on Outcomes in Acute Diverticulitis: Should Guidelines Be Revised? Dis. Colon Rectum 2019, 62, 71–78. [Google Scholar] [CrossRef]
  56. Masoomi, H.; Kang, C.Y.; Chen, A.; Mills, S.; Dolich, M.O.; Carmichael, J.C.; Stamos, M.J. Predictive factors of in-hospital mortality in colon and rectal surgery. J. Am. Coll. Surg. 2012, 215, 255–261. [Google Scholar] [CrossRef]
  57. McArdle, C.S.; Hole, D.J. Emergency presentation of colorectal cancer is associated with poor 5-year survival. BJS—Br. J. Surg. 2004, 91, 605–609. [Google Scholar] [CrossRef]
  58. Falanga, A.; Marchetti, M.; Vignoli, A. Coagulation, and cancer: Biological and clinical aspects. J. Thromb. Haemost.—JTH 2013, 11, 223–233. [Google Scholar] [CrossRef]
  59. Laino, L.; Cicciù, M.; Fiorillo, L.; Crimi, S.; Bianchi, A.; Amoroso, G.; Monte, I.P.; Herford, A.S.; Cervino, G. Surgical Risk on Patients with Coagulopathies: Guidelines on Hemophiliac Patients for Oro-Maxillofacial Surgery. Int. J. Environ. Res. Public Health 2019, 16, 1386. [Google Scholar] [CrossRef] [Green Version]
  60. Choi, J.S.; Bae, E.H.; Ma, S.K.; Kweon, S.S.; Kim, S.W. Prognostic impact of hyponatraemia in patients with colorectal cancer. Colorectal Dis. 2015, 17, 409–416. [Google Scholar] [CrossRef]
  61. Fucà, G.; Mariani, L.; Lo Vullo, S.; Galli, G.; Berardi, R.; Di Nicola, M.; Vernieri, C.; Morelli, D.; Dotti, K.; Fiordoliva, I.; et al. Weighing the prognostic role of hyponatremia in hospitalized patients with metastatic solid tumors: The HYPNOSIS study. Sci. Rep. 2019, 9, 12993. [Google Scholar] [CrossRef]
  62. Lasisi, F.; Rex, D.K. Improving protection against proximal colon cancer by colonoscopy. Expert Rev. Gastroenterol. Hepatol. 2011, 5, 745–754. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  63. Shergill, A.K.; Conners, E.E.; McQuaid, K.R.; Epstein, S.; Ryan, J.C.; Shah, J.N.; Inadomi, J.; Somsouk, M. Protective association of colonoscopy against proximal and distal colon cancer and patterns in interval cancer. Gastrointest. Endosc. 2015, 82, 529–537. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  64. Doubeni, C.A.; Corley, D.A.; Quinn, V.P.; Jensen, C.D.; Zauber, A.G.; Goodman, M.; Johnson, J.R.; Mehta, S.J.; Becerra, T.A.; Zhao, W.K.; et al. Effectiveness of screening colonoscopy in reducing the risk of death from right and left colon cancer: A large community-based study. Gut 2018, 67, 291–298. [Google Scholar] [CrossRef]
  65. Rex, D.K. Colonoscopy: The Current King of the Hill in the USA. Dig. Dis. Sci. 2015, 60, 639–646. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  66. Kirchhoff, P.; Clavien, P.A.; Hahnloser, D. Complications in colorectal surgery: Risk factors and preventive strategies. Patient Saf. Surg. 2010, 4, 5. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  67. D’Souza, N.; de Neree Tot Babberich, M.P.M.; Lord, A.; Shaw, A.; Abulafi, M.; Tekkis, P.; Wiggers, T.; Brown, G. The rectosigmoid problem. Surg. Oncol. 2018, 27, 521–525. [Google Scholar] [CrossRef] [PubMed]
  68. Kim, J.H. Controversial issues in radiotherapy for rectal cancer: A systematic review. Radiat. Oncol. J. 2017, 35, 295–305. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  69. Soyer, P.; Hamzi, L.; Sirol, M.; Duchat, F.; Dray, X.; Hristova, L.; Placé, V.; Pocard, M.; Boudiaf, M. Colon cancer: Comprehensive evaluation with 64-section CT colonography using water enema as intraluminal contrast agent-a pictorial review. Clin. Imaging 2012, 36, 113–125. [Google Scholar] [CrossRef]
  70. Feuerlein, S.; Grimm, L.J.; Davenport, M.S.; Haystead, C.M.; Miller, C.M.; Neville, A.M.; Jaffe, T.A. Can the localization of primary colonic tumors be improved by staging CT without specific bowel preparation compared to optical colonoscopy? Eur. J. Radiol. 2012, 81, 2538–2542. [Google Scholar] [CrossRef]
  71. Luna-Abanto, J. The rectosigmoid junction: Are limits important? Rev. Esp. Enferm. Dig. 2019, 111, 410. [Google Scholar] [CrossRef]
Table 1. Procedures of emergency admitted patients with the primary diagnosis of rectum or rectosigmoid junction.
Table 1. Procedures of emergency admitted patients with the primary diagnosis of rectum or rectosigmoid junction.
Operations on the Digestive System (ICD 9)
Operations on Esophagus (42.01–42.19, 42.31–42.99)
Operations on Stomach (43.0–44.03, 44.21–44.99)
Operations on Intestine (45.00–45.03, 45.30–46.99)
Operations on Appendix (47.01–47.99)
Operations on Rectum, Rectosigmoid, and Perirectal Tissue (48.0–48.1, 48.31–48.99)
Operations on Anus (49.01–49.12, 49.31–49.99)
Operations on Liver (50.0, 50.21–50.99)
Operations on Gallbladder and Biliary Tract (51.01–51.04, 51.21–51.99)
Operations on Pancreas (52.01–52.09, 52.21–52.99)
Operations on Hernia (53.00–53.9)
Operations on Other Operations on Abdominal Region (54.0–54.19, 54.3–54.99)
Invasive Diagnostic and Therapeutic Procedures on the Digestive System (ICD 9)
Invasive Diagnostic and/or Therapeutic Procedure on Esophagus (42.21–42.29)
Invasive Diagnostic and/or Therapeutic Procedure on Stomach (44.11–44.19)
Invasive Diagnostic and/or Therapeutic Procedure on Intestine (45.11–45.29)
Invasive Diagnostic and/or Therapeutic Procedure on Rectum, Rectosigmoid, and Perirectal Tissue (48.21–48.29)
Invasive Diagnostic and/or Therapeutic Procedure on Anus (49.21–49.29)
Invasive Diagnostic and/or Therapeutic Procedure on Liver (50.11–50.19)
Invasive Diagnostic and/or Therapeutic Procedure on Gallbladder and Biliary Tract (51.10–51.19)
Invasive Diagnostic and/or Therapeutic Procedure on Pancreas (52.11–52.19)
Invasive Diagnostic and/or Therapeutic Procedure on Other Operations on Abdominal Region (54.21–54.29)
Table 2. Characteristics of emergency admitted patients with the primary diagnosis of malignant neoplasm of rectum or rectosigmoid junction. Data (NIS 2005–2014) were stratified according to sex categories. * p < 0.05.
Table 2. Characteristics of emergency admitted patients with the primary diagnosis of malignant neoplasm of rectum or rectosigmoid junction. Data (NIS 2005–2014) were stratified according to sex categories. * p < 0.05.
Patients’ CharacteristicsAdult (18–64), N (%)Elderly (65+), N (%)
MaleFemaleMaleFemale
All Cases6705 (61.4%)4213 (38.6%)6708 (52.8%)5988 (47.2%)
RaceWhite3506 (59.9%) *2298 (63.2%) *4304 (74.9%) *3830 (74.8%) *
Black1040 (17.8%) *624 (17.2%) *574 (10.0%) *630 (12.3%) *
Hispanic805 (13.7%) *431 (11.9%) *490 (8.5%) *331 (6.5%) *
Asian/Pacific Islander269 (4.6%) *142 (3.9%) *203 (3.5%) *163 (3.2%) *
Native American51 (0.9%) *27 (0.7%) *34 (0.6%) *31 (0.6%) *
Other185 (3.2%) *112 (3.1%) *145 (2.5%) *133 (2.6%) *
Income
Quartile
Quartile 12144 (33.1%)1319 (32.1%)1943 (29.6%)1645 (28.0%)
Quartile 21717 (26.5%)1041 (25.3%)1775 (27.0%)1549 (26.4%)
Quartile 31466 (22.6%)957 (23.3%)1525 (23.2%)1384 (23.6%)
Quartile 41152 (17.8%)798 (19.4%)1326 (20.2%)1288 (22.0%)
InsurancePrivate Insurance2774 (41.5%) *1923 (45.8%) *639 (9.5%) *430 (7.2%) *
Medicare763 (11.4%) *426 (10.1%) *5800 (86.6%) *5313 (88.8%) *
Medicaid1781 (26.6%) *1095 (26.1%) *111 (1.7%) *127 (2.1%) *
Self-Pay882 (13.2%) *462 (11.0%) *50 (0.7%) *55 (0.9%) *
No Charge99 (1.5%) *58 (1.4%) *5 (0.1%) *5 (0.1%) *
Other384 (5.7%) *235 (5.6%) *90 (1.3%) *51 (0.9%) *
Hospital
Location
Rural673 (10.0%)399 (9.5%)905 (13.5%)778 (13.0%)
Urban: Non-Teaching2471 (36.9%)1493 (35.4%)2834 (42.2%)2616 (43.7%)
Urban: Teaching3561 (53.1%)2321 (55.1%)2969 (44.3%)2594 (43.3%)
ComorbiditiesAIDS92 (1.4%) *25 (0.6%) *4 (0.1%)0 (0%)
Alcohol Abuse580 (8.7%) *92 (2.2%) *286 (4.3%) *55 (0.9%) *
Deficiency Anemias1914 (28.5%) *1279 (30.4%) *2000 (29.8%)1802 (30.1%)
Rheumatoid Arthritis18 (0.3%) *68 (1.6%) *42 (0.6%) *144 (2.4%) *
Chronic Blood Loss635 (9.5%) *340 (8.1%) *827 (12.3%)793 (13.2%)
Congestive Heart Failure187 (2.8%)124 (2.9%)875 (13.0%)806 (13.5%)
Chronic Pulmonary Disease629 (9.4%) *452 (10.7%) *1367 (20.4%) *1021 (17.1%) *
Coagulopathy280 (4.2%)171 (4.1%)339 (5.1%) *240 (4.0%) *
Depression381 (5.7%) *457 (10.8%) *389 (5.8%) *476 (7.9%) *
Diabetes Uncomplicated896 (13.4%)555 (13.2%)1427 (21.3%) *1149 (19.2%) *
Diabetes, Chronic Complications125 (1.9%)59 (1.4%)190 (2.8%)155 (2.6%)
Drug Abuse269 (4.0%) *87 (2.1%) *24 (0.4%)13 (0.2%)
Hypertension2333 (34.8%)1439 (34.2%)3841 (57.3%) *3691 (61.6%) *
Hypothyroidism129 (1.9%) *289 (6.9%) *359 (5.4%) *930 (15.5%) *
Liver Disease331 (4.9%) *120 (2.8%) *139 (2.1%)99 (1.7%)
Lymphoma17 (0.3%)10 (0.2%)31 (0.5%)25 (0.4%)
Fluid/Electrolyte Disorders1958 (29.2%) *1385 (32.9%) *2262 (33.7%)2402 (40.1%)
Metastatic Cancer1552 (23.1%)967 (23.0%)1214 (18.1%)1051 (17.6%)
Other Neurological Disorders210 (3.1%) *162 (3.8%) *435 (6.5%) *477 (8.0%) *
Obesity374 (5.6%) *346 (8.2%) *252 (3.8%) *327 (5.5%) *
Paralysis69 (1.0%)43 (1.0%)138 (2.1%)106 (1.8%)
Peripheral Vascular Disorders143 (2.1%) *56 (1.3%) *533 (7.9%) *357 (6.0%) *
Psychoses227 (3.4%) *179 (4.2%) *160 (2.4%)168 (2.8%)
Pulmonary Circulation Disorder80 (1.2%)53 (1.3%)188 (2.8%)190 (3.2%)
Renal Failure293 (4.4%) *109 (2.6%) *851 (12.7%) *537 (9.0%) *
Solid Tumor74 (1.1%)49 (1.2%)122 (1.8%)83 (1.4%)
Peptic Ulcer1 (0.0%)2 (0.0%)10 (0.1%)6 (0.1%)
Valvular Disease85 (1.3%)65 (1.5%)455 (6.8%)432 (7.2%)
Weight Loss1095 (16.3%) *595 (14.1%) *1200 (17.9%)993 (16.6%)
Neoplasm
Location
Rectosigmoid Junction2870 (42.8%) *1886 (44.8%) *2703 (40.3%) *2533 (42.3%) *
Rectum3835 (57.2%) *2327 (55.2%) *4005 (59.7%) *3455 (57.7%) *
Invasive Diagnostic and/or Therapeutic Procedures on GI3477 (51.9%) *1997 (47.4%) *3699 (55.1%)3382 (56.5%)
GI System Operation3746 (55.9%) *2259 (53.6%) *3930 (58.6%) *3304 (55.2%) *
Deceased288 (4.3%)207 (4.9%)428 (6.4%)335 (5.6%)
Mean (SD)Mean (SD)Mean (SD)Mean (SD)
Age, Years53.03 (8.41) *52.59 (8.78) *76.24 (7.56) *78.72 (8.12) *
Time to Invasive Diagnostic and/or Therapeutic Procedure, Days2.03 (2.94)2.18 (3.16)2.26 (2.90)2.37 (2.65)
Time to Surgical Procedure, Days2.51 (3.95)2.55 (3.56)2.92 (3.96) *3.28 (3.76) *
Hospital Length of Stay, Days8.67 (9.09)8.56 (10.05)9.44 (9.06)9.18 (7.73)
Total Charges, USD64,420
(99,057)
60,456
(81,658)
66,654
(91,353)
60,625
(69,078)
Table 3. Characteristics of emergency admitted patients with the primary diagnosis of malignant neoplasm of rectum or rectosigmoid junction. Data (NIS 2005–2014) were stratified according to outcome categories. * p < 0.05.
Table 3. Characteristics of emergency admitted patients with the primary diagnosis of malignant neoplasm of rectum or rectosigmoid junction. Data (NIS 2005–2014) were stratified according to outcome categories. * p < 0.05.
Patients’ CharacteristicsAdult (18–64), N (%)Elderly (65+), N (%)
SurvivedDeceasedSurvivedDeceased
All Cases10,419 (95.5%)495 (4.5%)11,933 (94.0%)763 (6.0%)
Sex, Female4003 (38.4%)207 (41.8%)5650 (47.4%)335 (43.9%)
RaceWhite5517 (60.9%)284 (66.7%)7622 (74.6%)508 (78.3%)
Black1598 (17.6%)65 (15.3%)1146 (11.2%)58 (8.9%)
Hispanic1194 (13.2%)42 (9.9%)778 (7.6%)42 (6.5%)
Asian/Pacific Islander389 (4.3%)21 (4.9%)350 (3.4%)16 (2.5%)
Native American77 (0.8%)1 (0.2%)59 (0.6%)6 (0.9%)
Other284 (3.1%)13 (3.1%)259 (2.5%)19 (2.9%)
Income
Quartile
Quartile 13321 (32.9%)142 (29.3%)3372 (28.9%)220 (29.4%)
Quartile 22626 (26.0%)132 (27.2%)3120 (26.7%)202 (27.0%)
Quartile 32316 (22.9%)106 (21.9%)2749 (23.5%)160 (21.4%)
Quartile 41844 (18.2%)105 (21.6%)2446 (20.9%)167 (22.3%)
InsurancePrivate Insurance4541 42.8(%)242 (49.6%)967 (8.1%) *102 (13.4%) *
Medicare1135 (10.9%)54 (11.1%)10,501 (88.1%) *612 (80.4%) *
Medicaid2776 (26.7%)103 (21.1%)226 (1.9%) *12 (1.6%) *
Self-Pay1290 (12.4%)53 (10.9%)96 (0.8%) *9 (1.2%) *
No Charge153 (1.5%)4 (0.8%)9 (0.1%) *1 (0.1%) *
Other585 (5.6%)32 (6.6%)116 (1.0%) *25 (3.3%) *
Hospital
Location
Rural1002 (9.6%)70 (14.1%)1560 (13.1%)123 (16.1%)
Urban: Non-Teaching3799 (36.5%)161 (32.5%)5128 (43.0%)320 (41.9%)
Urban: Teaching5618 (53.9%)264 (53.3%)5245 (44.0%)320 (41.9%)
ComorbiditiesAIDS113 (1.1%)4 (0.8%)3 (0.0%)1 (0.1%)
Alcohol Abuse652 (6.3%)20 (4.0%)329 (2.8%)12 (1.6%)
Deficiency Anemias3080 (29.6%)111 (22.4%)3622 (30.4%) *179 (23.5%) *
Rheumatoid Arthritis84 (0.8%)2 (0.4%)180 (1.5%)6 (0.8%)
Chronic Blood Loss955 (9.2%) *20 (4.0%) *1564 (13.1%) *56 (7.3%) *
Congestive Heart Failure288 (2.8%)23 (4.6%)1546 (13.0%) *135 (17.7%) *
Chronic Pulmonary Disease1037 (10.0%)42 (8.5%)2237 (18.7%)151 (19.8%)
Coagulopathy372 (3.6%) *79 (16.0%) *490 (4.1%) *88 (11.5%) *
Depression823 (7.9%) *16 (3.2%) *815 (6.8%)49 (6.4%)
Diabetes, Uncomplicated1403 (13.5%)46 (9.3%)2465 (20.7%) *111 (14.5%) *
Diabetes, Chronic Complications172 (1.7%)12 (2.4%)334 (2.8%)11 (1.4%)
Drug Abuse350 (3.4%)6 (1.2%)35 (0.3%)2 (0.3%)
Hypertension3645 (35.0%) *125 (25.3%) *7181 (60.2%) *351 (46.0%) *
Hypothyroidism400 (3.8%)18 (3.6%)1230 (10.3%)59 (7.7%)
Liver Disease395 (3.8%) *56 (11.3%) *208 (1.7%) *30 (3.9%) *
Lymphoma25 (0.2%)2 (0.4%)51 (0.4%)5 (0.7%)
Fluid/Electrolyte Disorders3079 (29.6%) *263 (53.1%) *4268 (35.8%) *392 (51.4%) *
Metastatic Cancer2434 (23.4%) *81 (16.4%) *2120 (17.8%)145 (19.0%)
Other Neurological Disorders339 (3.3%) *33 (6.7%) *844 (7.1%)68 (8.9%)
Obesity689 (6.6%)31 (6.3%)564 (4.7%) *15 (2.0%) *
Paralysis104 (1.0%)7 (1.4%)230 (1.9%)14 (1.8%)
Peripheral Vascular Disorders187 (1.8%)12 (2.4%)832 (7.0%)58 (7.6%)
Psychoses389 (3.7%)17 (3.4%)298 (2.5%)30 (3.9%)
Pulmonary Circulation Disorder115 (1.1%) *18 (3.6%) *336 (2.8%) *42 (5.5%) *
Renal Failure369 (3.5%) *33 (6.7%) *1281 (10.7%)106 (13.9%)
Solid Tumor119 (1.1%)3 (0.6%)196 (1.6%)9 (1.2%)
Peptic Ulcer3 (0.0%)0 (0%)16 (0.1%)0 (0%)
Valvular Disease146 (1.4%)4 (0.8%)846 (7.1%)41 (5.4%)
Weight Loss1593 (15.3%)97 (19.6%)1996 (16.7%) *194 (25.4%) *
Neoplasm
Location
Rectosigmoid Junction4480 (43.0%) *273 (55.2%) *4851 (40.7%) *382 (50.1%) *
Rectum5939 (57.0%) *222 (44.8%) *7082 (59.3%) *381 (49.9%) *
Invasive Diagnostic and/or Therapeutic Procedures on GI5373 (51.6%) *99 (20.0%) *6791 (56.9%) *288 (37.7%) *
GI System Operation5847 (56.1%) *154 (31.1%) *6855 (57.4%) *379 (49.7%) *
Mean (SD)Mean (SD)Mean (SD)Mean (SD)
Age, Years52.81 (8.57)53.87 (8.05)77.34 (7.92) *78.55 (8.00) *
Time to Invasive Diagnostic and/or Therapeutic Procedure, Days2.04 (2.83) *4.25 (7.81) *2.26 (2.61) *3.44 (5.37) *
Time to First Surgical Procedure, Days2.47 (3.58)4.49 (8.57)2.97 (3.69) *5.04 (6.04) *
Hospital Length of Stay, Days8.52 (8.88)10.89 (17.69)9.18 (8.21)11.47 (11.44)
Total Charges, USD62,082
(88,996) *
80,183
(151,679) *
62,206
(76,350)
88,847
(138,226)
Table 4. Characteristics of emergency admitted patients with the primary diagnosis of malignant neoplasm of rectum or rectosigmoid junction. Data (NIS 2005–2014) were stratified according to surgery status. * p < 0.05.
Table 4. Characteristics of emergency admitted patients with the primary diagnosis of malignant neoplasm of rectum or rectosigmoid junction. Data (NIS 2005–2014) were stratified according to surgery status. * p < 0.05.
Patients’ CharacteristicsAdult (18–64), N (%)Elderly (65+), N (%)
No OperationOperationNo OperationOperation
All Cases4915 (45.0%)6007 (55.0%)5463 (43.0%)7238 (57.0%)
Sex, Female1954 (39.8%)2259 (37.6%)2684 (49.1%) *3304 (45.7%) *
RaceWhite2448 (57.0%) *3357 (64.6%) *3422 (72.7%) *4712 (76.5%) *
Black882 (20.6%) *782 (15.0%) *624 (13.3%) *580 (9.4%) *
Hispanic607 (14.1%) *629 (12.1%) *351 (7.5%) *470 (7.6%) *
Asian/Pacific Islander186 (4.3%) *225 (4.3%) *155 (3.3%) *211 (3.4%) *
Native American31 (0.7%) *47 (0.9%) *24 (0.5%) *41 (0.7%) *
Other137 (3.2%) *160 (3.1%) *131 (2.8%) *147 (2.4%) *
Income
Quartile
Quartile 11585 (33.4%)1881 (32.1%)1545 (28.9%)2047 (28.8%)
Quartile 21210 (25.5%)1549 (26.4%)1355 (25.4%)1969 (27.7%)
Quartile 31072 (22.6%)1351 (23.1%)1248 (23.4%)1661 (23.4%)
Quartile 4874 (18.4%)1076 (18.4%)1194 (22.4%)1421 (20.0%)
InsurancePrivate Insurance1900 (38.8%) *2797 (46.7%) *498 (9.1%) *571 (7.9%) *
Medicare616 (12.6%) *573 (9.6%) *4695 (86.1%) *6423 (88.9%) *
Medicaid1420 (29.0%) *1460 (24.4%) *121 (2.2%) *117 (1.6%) *
Self-Pay610 (12.5%) *734 (12.3%) *51 (0.9%) *54 (0.7%) *
No Charge77 (1.6%) *80 (1.3%) *3 (0.1%) *7 (0.1%) *
Other275 (5.6%) *344 (5.7%) *85 (1.6%) *56 (0.8%) *
Hospital
Location
Rural455 (9.3%)617 (10.3%)704 (12.9%)979 (13.5%)
Urban: Non-Teaching1730 (35.2%)2234 (37.2%)2297 (42.0%)3154 (43.6%)
Urban: Teaching2730 (55.5%)3156 (52.5%)2462 (45.1%)3105 (42.9%)
ComorbiditesAIDS83 (1.7%) *34 (0.6%) *2 (0.0%)2 (0.0%)
Alcohol Abuse276 (5.6%)396 (6.6%)155 (2.8%)186 (2.6%)
Deficiency Anemias1550 (31.5%) *1643 (27.4%) *1724 (31.6%)2078 (28.7%)
Rheumatoid Arthritis46 (0.9%)40 (0.7%)80 (1.5%)106 (1.5%)
Chronic Blood Loss496 (10.1%) *479 (8.0%) *786 (14.4%) *834 (11.5%) *
Congestive Heart Failure133 (2.7%)178 (3.0%)674 (12.3%)1007 (13.9%)
Chronic Pulmonary Disease424 (8.6%) *657 (10.9%) *914 (16.7%) *1474 (20.4%) *
Coagulopathy213 (4.3%)238 (4.0%)224 (4.1%)355 (4.9%)
Depression387 (7.9%)452 (7.5%)432 (7.9%) *433 (6.0%) *
Diabetes, Uncomplicated644 (13.1%)807 (13.4%)1096 (20.1%)1480 (20.4%)
Diabetes, Chronic Complications83 (1.7%)101 (1.7%)141 (2.6%)204 (2.8%)
Drug Abuse177 (3.6%)179 (3.0%)21 (0.4%)16 (0.2%)
Hypertension1635 (33.3%)2137 (35.6%)3104 (56.8%) *4429 (61.2%) *
Hypothyroidism201 (4.1%)217 (3.6%)567 (10.4%)722 (10.0%)
Liver Disease193 (3.9%)258 (4.3%)107 (2.0%)131 (1.8%)
Lymphoma11 (0.2%)16 (0.3%)22 (0.4%)34 (0.5%)
Fluid/Electrolyte Disorders1549 (31.5%)1794 (29.9%)1900 (34.8%) *2765 (38.2%) *
Metastatic Cancer204 (4.2%) *2315 (38.5%) *123 (2.3%) *2144 (29.6%) *
Other Neurological Disorders189 (3.8%)183 (3.0%)427 (7.8%)485 (6.7%)
Obesity253 (5.1%) *467 (7.8%) *177 (3.2%) *402 (5.6%) *
Paralysis58 (1.2%)54 (0.9%)116 (2.1%)128 (1.8%)
Peripheral Vascular Disorders73 (1.5%)126 (2.1%)377 (6.9%)513 (7.1%)
Psychoses194 (3.9%)212 (3.5%)143 (2.6%)185 (2.6%)
Pulmonary Circulation Disorder58 (1.2%)75 (1.2%)141 (2.6%)237 (3.3%)
Renal Failure203 (4.1%)199 (3.3%)631 (11.6%)757 (10.5%)
Solid Tumor6 (0.1%) *117 (1.9%) *11 (0.2%) *194 (2.7%) *
Peptic Ulcer2 (0.0%)1 (0.0%)9 (0.2%)7 (0.1%)
Valvular Disease57 (1.2%)93 (1.5%)301 (5.5%) *586 (8.1%) *
Weight Loss739 (15.0%)951 (15.8%)859 (15.7%) *1334 (18.4%) *
Neoplasm
Location
Rectosigmoid Junction1872 (38.1%) *2887 (48.1%) *1876 (34.3%) *3361 (46.4%) *
Rectum3043 (61.9%) *3120 (51.9%) *3587 (65.7%) *3877 (53.6%) *
Invasive Diagnostic and/or Therapeutic Procedures on GI2226 (45.3%) *3249 (54.1%) *2827 (51.7%) *4254 (58.8%) *
Deceased341 (6.9%) *154 (2.6%) *384 (7.0%) *379 (5.2%) *
Mean (SD)Mean (SD)Mean (SD)Mean (SD)
Age, Years52.50 (8.74) *53.15 (8.39) *78.09 (8.19) *76.90 (7.69) *
Time to Invasive Diagnostic and/or Therapeutic Procedure, Days2.07 (2.45) *2.10 (3.38) *2.28 (2.39)2.33 (3.03)
Hospital Length of Stay, Days6.04 (7.30) *10.75 (10.46) *6.05 (5.91) *11.78 (9.23) *
Total Charges, USD36,314
(47,212) *
84,344
(113,048) *
33,643
(37,915) *
86,498
(96,956) *
Table 5. Backward logistic regression analysis to evaluate the associations between mortality and different risk factors in patients emergently admitted with a primary diagnosis of malignant neoplasm of rectum or rectosigmoid junction and undergoing an operation (NIS 2004–2014). Mortality was the dependent variable.
Table 5. Backward logistic regression analysis to evaluate the associations between mortality and different risk factors in patients emergently admitted with a primary diagnosis of malignant neoplasm of rectum or rectosigmoid junction and undergoing an operation (NIS 2004–2014). Mortality was the dependent variable.
Patients’ Characteristics Mortality in Adults Patients with OperationMortality in Elderly Patients with Operation
N = 6619R2 = 0.249N = 8167R2 = 0.186
OR (95% CI)pOR (95% CI)p
Number of EventsN = 205N = 485
Age, YearsRemoved1.03 (1.02, 1.05)<0.001
Invasive Diagnostic and/or Therapeutic Procedure0.49 (0.35, 0.67)<0.0010.82 (0.66, 1.01)0.070
Time to First Surgical Operation, Days1.04 (1.02, 1.07)<0.0011.05 (1.03, 1.07)<0.001
Sex, FemaleRemoved0.78 (0.63, 0.96)0.019
Bacterial Infections (Other than Tuberculosis)2.94 (1.99, 4.34)<0.0012.53 (1.99, 3.21)<0.001
Respiratory Diseases2.83 (2.02, 3.98)<0.0012.61 (2.08, 3.28)<0.001
Coagulopathy1.58 (1.03, 2.43)0.0361.48 (1.12, 1.95)0.006
Cardiac Diseases1.93 (1.39, 2.70)<0.0011.67 (1.33, 2.10)<0.001
Fluid and Electrolyte Disorders1.84 (1.31, 2.60)<0.0011.82 (1.46, 2.26)<0.001
Genitourinary System Diseases1.32 (0.95, 1.84)0.1001.29 (1.04, 1.60)0.020
Trauma, Burns, and Poisons1.43 (0.99, 2.07)0.0601.86 (1.48, 2.33)<0.001
Liver Diseases2.51 (1.64, 3.85)<0.001Removed Via
Stepwise
Backward
Elimination
Neoplasms2.42 (1.67, 3.50)<0.001
Neurological Diseases1.99 (1.34, 2.96)<0.001
Neoplasm of Rectosigmoid JunctionRemoved Via
Stepwise
Backward
Elimination
Digestive Diseases other than Liver
Hypertension
Anemia and/or Hemorrhage
Musculoskeletal System and Connective Tissue Diseases
Tobacco Use
Psychiatric Diseases
Endocrine Diseases
Tuberculosis
Nonbacterial Infections
Peripheral Vascular Diseases
Diabetes
Alcohol Abuse/Withdrawal/Dependence
Drug Abuse/Withdrawal/Dependence
Nutritional/Weight Disorders
Platelet and White Blood Cell Diseases
Skin Diseases
Medications
Diseases of Oral Cavity, Salivary Glands, and Jaw
Cerebrovascular Diseases
Sleep Disorders
Lack of Physical Evidence
Inappropriate Diet and Eating Habits
High Risk Lifestyle Behaviors
Social Factors
Body Mass Index
Table 6. Backward logistic regression analysis to evaluate the associations between mortality and different factors in patients emergently admitted with a primary diagnosis of malignant neoplasm of rectum or rectosigmoid junction and not undergoing an operation (NIS 2004–2014). Mortality was the dependent variable.
Table 6. Backward logistic regression analysis to evaluate the associations between mortality and different factors in patients emergently admitted with a primary diagnosis of malignant neoplasm of rectum or rectosigmoid junction and not undergoing an operation (NIS 2004–2014). Mortality was the dependent variable.
Patients’ Characteristics Mortality in Adult Patients with No OperationMortality in Elderly Patients with No Operation
N = 5867R2 = 0.210N = 6873R2 = 0.191
OR (95% CI)pOR (95% CI)p
Number of EventsN = 419N = 521
Age, YearsRemoved1.01 (1.00, 1.03)0.032
Invasive Diagnostic and/or Therapeutic Procedures0.13 (0.09, 0.18)<0.0010.19 (0.15, 0.24)<0.001
Hospital Length of Stay, Days1.01 (0.99, 1.02)0.0601.02 (1.01, 1.03)0.002
Malignant Neoplasm of Rectosigmoid Junction1.36 (1.10, 1.68)0.0051.51 (1.25, 1.83)<0.001
Respiratory Diseases2.06 (1.63, 2.59)<0.0011.78 (1.47, 2.16)<0.001
Fluid and Electrolyte Disorders1.62 (1.31, 2.01)<0.0011.44 (1.19, 1.73)<0.001
Neoplasms2.22 (1.68, 2.94)<0.0011.25 (1.03, 1.53)0.028
Liver Diseases1.95 (1.39, 2.73)<0.001Removed Via
Stepwise
Backward
Elimination
Coagulopathy1.60 (1.17, 2.18)0.003
Cardiac Diseases1.55 (1.20, 2.00)<0.001
Neurological Diseases1.34 (1.00, 1.80)0.047
Skin Diseases1.42 (1.05, 1.91)0.023
Trauma, Burns, and Poisons 1.82 (1.33, 2.47)<0.001
Sex, FemaleRemoved Via
Stepwise
Backward
Elimination
1.89 (1.45, 2.46)<0.001
Neoplasm of Rectosigmoid Junction1.47 (1.09, 1.96)0.011
Bacterial Infections (Other than Tuberculosis)Removed Via
Stepwise
Backward
Elimination
Platelet and White Blood Cell Diseases
Diseases of Oral Cavity, Salivary Glands, and Jaw
Anemia and/or Hemorrhage
Digestive Diseases other than Liver
Tobacco Use
Hypertension
Endocrine Diseases
Musculoskeletal System and Connective Tissue Diseases
Social Factors
Medications
Psychiatric Diseases
Cerebrovascular Diseases
Nonbacterial Infections
Alcohol Abuse/Withdrawal/Dependence
Peripheral Vascular Diseases
Diabetes
Drug Abuse/Withdrawal/Dependence
Genitourinary System Diseases
Tuberculosis
Nutritional/Weight Disorders
Sleep Disorders
Lack of Physical Evidence
Inappropriate Diet and Eating Habits
High Risk Lifestyle Behaviors
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Levy, L.; Smiley, A.; Latifi, R. Adult and Elderly Risk Factors of Mortality in 23,614 Emergently Admitted Patients with Rectal or Rectosigmoid Junction Malignancy. Int. J. Environ. Res. Public Health 2022, 19, 9203. https://doi.org/10.3390/ijerph19159203

AMA Style

Levy L, Smiley A, Latifi R. Adult and Elderly Risk Factors of Mortality in 23,614 Emergently Admitted Patients with Rectal or Rectosigmoid Junction Malignancy. International Journal of Environmental Research and Public Health. 2022; 19(15):9203. https://doi.org/10.3390/ijerph19159203

Chicago/Turabian Style

Levy, Lior, Abbas Smiley, and Rifat Latifi. 2022. "Adult and Elderly Risk Factors of Mortality in 23,614 Emergently Admitted Patients with Rectal or Rectosigmoid Junction Malignancy" International Journal of Environmental Research and Public Health 19, no. 15: 9203. https://doi.org/10.3390/ijerph19159203

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop