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ARTICLE: COLON

A Novel Multiparameter Scoring Model for Noninvasive Early Prediction of Ischemic Colitis: A Multicenter, Retrospective, and Real-World Study

Li, Shan MB1; Luo, Yiwei MM1; Wang, Wei MB1; Lu, Jinlai MM1; Hu, Miao MD1; Sun, Qinjuan MM1; Yang, Xiaoqing MB1; Han, Junyi MD; Zhong, Lan MD1

Author Information
Clinical and Translational Gastroenterology: June 2021 - Volume 12 - Issue 6 - p e00370
doi: 10.14309/ctg.0000000000000370
  • Open

Abstract

INTRODUCTION

Ischemic colitis (IC) is a common form of intestinal ischemic injury. In general, the disease is transient and self-limited. Symptoms and signs of IC can improve within 1–2 weeks of fasting, parenteral nutrition, and even antibiotic treatment. In a few cases, severe consequences such as peritonitis, right colon ischemia, stenosis and necrosis of the colon, renal dysfunction, and Clostridium difficile infection associated with high recurrence and mortality rates can occur and may require surgical treatment (1–3). Mortality rates of patients with segmental necrosis range from 20% to 39% (4). Therefore, we have attempted to identify factors influencing IC prognoses during the early stages of the disease.

Colonoscopy is the gold standard for diagnosing IC. Early use of colonoscopy (within 48 hours of symptom onset) reduced mortality, hospital stay lengths, and hospital costs (5). Outcomes of IC seem to depend on several factors, including clinical symptoms, endoscopic ischemic sites, comorbidities, and medications. Previous studies showed that hyperthyroidism, stroke, chronic obstructive pulmonary disease, and complications involving small intestinal lesions might be independent risk factors for high mortality (6,7). Peixoto et al. (8) noted that atrial fibrillation, admission to the intensive care unit, and use of vasopressin drugs were independently associated with inpatient mortality, and a predicted case fatality rate of 32% was observed when all 3 risk factors were present.

Despite these findings, there are no reports presenting both internally and externally validated scoring models with good efficacy for predicting adverse outcomes of IC. Therefore, this study aimed to establish and validate a prognostic scoring model that could be used to screen patients with IC and identify those requiring intensive treatment or surgery for severe disease in clinical practice.

METHODS

Patients diagnosed with IC by colonoscopy or surgery from November 2008 to May 2020 were identified from the clinical database of Shanghai Changzheng Hospital, Shanghai, China, and Shanghai East Hospital, Shanghai, China (n = 385). This study was approved by the Ethics Review Committee of both hospitals. The process used to select patients for developing the model is shown in Figure 1. Eighty-four patients were excluded, and the internal cohort (n = 260) was enrolled from Shanghai East Hospital. Forty-one patients from Shanghai Changzheng Hospital constituted an external cohort. Severe IC was considered to be present in patients who remained hospitalized for more than 14 days without a clinical cure, those who underwent an open or an interventional surgery, and those who died during hospitalization. Discharge criteria for the included patients were the disappearance of abdominal symptoms and signs, resumption of usual diet, and negative fecal occult blood test results.

Figure 1.
Figure 1.:
Process used to select the study participants for the prognostic model.

Clinical data of all patients were collected during the first 48 hours of admission. Clinical characteristics included age and sex, symptoms, history of abdominal surgery (within the previous month), history of drug use, comorbidities, history of smoking, history of alcohol consumption, laboratory variables, the severity of endoscopic ischemia, and location of the lesion.

All variables are divided into categorical variables (Table 1). Quantitative variables were divided into 2 groups bounded by their normal upper or lower limits. This classification helped clinicians to visually identify variable groups with high statistical significance. We showed the benefits of dichotomous variables by using a nomogram (Figure 2).

Table 1. - Patient characteristics at the baseline
Variable Mild (n = 176) Severe (n = 84) Statistic P value
Sex, n (%) 4.07 0.0436
 Female 121 (68.75) 47 (55.95)
 Male 55 (31.25) 37 (44.05)
Age, yr, n (%) 6.59 0.0103
 Younger than 65 years 97 (55.11) 32 (38.10)
 65 years or older 79 (44.89) 52 (61.90)
Laboratory findings, n (%)
 N > 6.3 × 109/L 40 (22.73) 63 (75.00) 64.95 <0.0001
 PLT <125 × 109/L 10 (5.68) 10 (11.90) 3.10 0.0782
 L < 1.1 × 109/L 27 (15.34) 29 (34.52) 12.38 0.0004
 NLR ≥5 25 (14.20) 59 (70.24) 81.63 <0.0001
 NLR ≥7 13 (7.39) 38 (45.24) 51.67 <0.0001
 NLR ≥10 3 (1.70) 21 (25.00) 36.83 <0.0001
 PLR ≥80 149 (84.66) 78 (92.86) 3.45 0.0633
 PLR ≥100 128 (72.73) 68 (80.95) 2.07 0.1499
 PLR ≥120 92 (52.27) 56 (66.67) 4.80 0.0284
 CRP (mg/L) 58.65 <0.0001
  <10 127 (72.16) 21 (25.00)
  10–50 37 (21.02) 33 (39.29)
  >50 12 (6.82) 30 (35.71)
 WBC count >9.5 × 109/L 29 (16.48) 51 (60.71) 52.24 <0.0001
 Hb level <115 (F)/130 (M) g/L 87 (49.43) 40 (47.62) 0.07 0.7845
 SCr level ≥110 (M)/92 (F) μmol/L 14 (7.95) 13 (15.48) 3.46 0.0630
 LDH level ≥ 250 U/L 31 (17.61) 19 (22.62) 0.92 0.3382
 Alb level <35 g/L 30 (17.05) 29 (34.52) 9.90 0.0017
 BUN level ≥7.1 (M)/6.1 (F) mol/L 11 (6.25) 18 (21.43) 13.22 0.0003
 D-dimer level ≥0.55 mg/L 100 (56.82) 82 (97.62) 45.08 <0.0001
 Na+ level <137 mmol/L 23 (13.07) 23 (27.38) 8.00 0.0047
 HR >100 beats/min 10 (5.68) 10 (11.90) 3.10 0.0782
Comorbidities, n (%)
 Hypertension 69 (39.20) 43 (51.19) 3.33 0.0680
 Diabetes mellitus 14 (7.95) 11 (13.10) 1.73 0.1885
 CAD 37 (21.02) 21 (25.00) 0.52 0.4713
 Atrial fibrillation 5 (2.84) 5 (5.95) 0.77 0.3814
 COPD 3 (1.70) 4 (4.76) 1.03 0.3102
 Intestinal surgery 10 (5.68) 8 (9.52) 1.30 0.2538
 CKD 2 (1.14) 2 (2.38) 0.05 0.8229
 Stroke 14 (7.95) 12 (14.29) 2.53 0.1115
 Depression 6 (3.41) 0 (0.00) 1.61 0.2039
 Hypothyroidism 3 (1.70) 1 (1.19) 0.00 1.0000
 Hepatitis B 6 (3.41) 3 (3.57) 0.00 1.0000
Medications, n (%)
 NSAIDs 18 (10.23) 10 (11.90) 0.17 0.6832
 CCBs 28 (15.91) 17 (20.24) 0.74 0.3882
 β-blockers 11 (6.25) 9 (10.71) 1.60 0.2065
 ARBs 31 (17.61) 10 (11.90) 1.40 0.2375
Lifestyle habits, n (%)
 Alcohol consumption 10 (5.68) 3 (3.57) 0.18 0.6702
 Smoking 24 (13.64) 8 (9.52) 0.89 0.3452
Symptoms, n (%)
 Stomach ache 152 (86.36) 73 (86.90) 0.01 0.9048
 Diarrhea 110 (62.50) 49 (58.33) 0.42 0.5192
 Hematochezia 140 (79.55) 63 (75.00) 0.69 0.4074
 Vomiting 41 (23.30) 26 (30.95) 1.74 0.1868
 Constipation 5 (2.84) 6 (7.14) 1.64 0.1998
Location, n (%)
 Distal ileum 9 (5.11) 12 (14.29) 6.44 0.0111
 Ascending colon 7 (3.98) 20 (23.81) 24.03 <0.0001
 Hepatic flexure 7 (3.98) 18 (21.43) 19.93 <0.0001
 Transverse colon 32 (18.18) 29 (34.52) 8.46 0.0036
 Splenic flexure 40 (22.73) 32 (38.10) 6.71 0.0096
 Descending colon 89 (50.57) 47 (55.95) 0.66 0.4163
 Sigmoid colon 111 (63.07) 40 (47.62) 5.57 0.0182
 Rectosigmoid junction 9 (5.11) 3 (3.57) 0.06 0.8117
Endoscopic findings, n (%)
 Erosion 84 (47.73) 37 (44.05) 0.31 0.5780
 Ulceration 41 (23.30) 45 (53.57) 23.55 <0.0001
 Stenosis 6 (3.41) 42 (50.00) 82.00 <0.0001
 Necrosis 0 (0.00) 10 (11.90) 18.69 <0.0001
CTA of SMA 3.06 0.0022
 Not evaluated 96 (54.55) 35 (41.67)
 No abnormal changes 42 (23.86) 17 (20.24)
 Atherosclerosis 30 (17.05) 12 (14.29)
 ≤70% stenosis 8 (4.55) 7 (8.33)
 >70% stenosis 0 (0.00) 4 (4.76)
 Embolism 0 (0.00) 9 (10.71)
Alb, albumin; ARBs, angiotensin receptor blockers; BUN, blood urea nitrogen; CAD, coronary artery disease; CCBs, calcium channel blockers; CKD, chronic kidney disease; COPD, chronic obstructive pulmonary disease; CRP, C-reactive protein; CTA, computed tomography angiography; F, female; Hb, hemoglobin; HR, heart rate; L, lymphocyte count; LDH, lactate dehydrogenase; M, male; N, neutrophil count; NLR, neutrophil-to-lymphocyte ratio; NSAIDs, nonsteroidal anti-inflammatory drugs; PLR, platelet-to-lymphocyte ratio; PLT, platelet count; SCr, serum creatinine; SMA, superior mesenteric arteriography; WBC, white blood cell.

Figure 2.
Figure 2.:
Endoscopic findings of patients with mild IC and those who were critically ill. (a) Local hyperemia and edema of the intestinal mucosa. (b) Erosion of intestinal mucosa. (c) Deep linear ulceration along the longitudinal axis of the colon. (d) Enteric stenosis through which the endoscope cannot be passed. (e) Extensive mucosal necrosis. (f) Coexistence of the aforementioned ischemic manifestations. Image courtesy of the Endoscopy Center, Shanghai East Hospital, China.

Statistical analysis

Univariate analysis.

Continuous variables were expressed as the mean ± SD or as the median (interquartile range) based on the data distribution. The independent-samples t test or Wilcoxon rank-sum test were used for comparisons. Categorical data were described as the frequency (percentage). Comparisons between the 2 groups were performed using the χ2 test or Fisher exact test.

Development of the prognostic model.

Variables with P < 0.05 according to the univariate analysis were selected for inclusion in the multivariate logistic regression analysis. The stepwise method was used to select the variables. The entry criterion was P < 0.1, and the exclusion criterion was P > 0.1. A nomogram was used to construct a prediction model based on the results of the multivariate logistic regression analysis.

Internal cross-validation and external validation.

In this study, 5-fold cross-validation was used as the internal validation method. A subset containing 80% of the cohort was randomly selected for training. The remaining 20% were selected for testing. The cross-validation process was repeated 5 times. External validation was performed using data from Shanghai Changzheng Hospital. Sensitivity, specificity, accuracy, Youden index, kappa coefficient, and areas under the receiver-operating characteristic curves (AUROCs) were used to evaluate the predictive ability of the model. All tests were 2-tailed, and P < 0.05 was considered statistically significant.

All statistical analyses and data management were performed using SAS version 9.4 (SAS Institute, Cary, NC). The nomogram was constructed using the rms package in R software version 4.0.1 (R Foundation for Statistical Computing, Vienna, Austria).

RESULTS

Demographic and clinical characteristics at baseline

Two-hundred sixty patients (168 women) with a mean age of 64.5 ± 12.2 years (range, 24–91 years) with IC were enrolled in the internal cohort. Fourteen patients underwent interventional/surgical procedures, and 3 patients died postoperatively. The mortality rate within 2 weeks of hospitalization was 2.6%. Demographic and clinical characteristics of patients with different outcomes are summarized in Table 1. Clinical details of quantitative variables are shown in Table 2.

Table 2. - Detailed clinical features of the internal cohort of ischemic colitis
Variable Mild (n = 176) Severe (n = 84)
Age (yr) 62.89 ± 11.69 67.73 ± 12.61
N (×109/L) 4.72 ± 2.44 8.88 ± 3.68
PLT (×109/L) 207.18 ± 68.06 197.60 ± 62.82
L (×109/L) 1.65 ± 0.59 1.37 ± 0.61
CRP level (mg/L) 13.44 ± 20.89 50.95 ± 59.42
WBC count (×109/L) 6.82 ± 2.80 11.04 ± 3.97
Hb (g/L) 127.32 ± 16.49 122.21 ± 23.09
NLR 3.32 ± 2.85 8.61 ± 8.27
PLR 142.20 ± 78.90 183.94 ± 143.14
SCr level (μmol/L) 72.38 ± 16.34 78.08 ± 30.36
LDH level (U/L) 202.66 ± 82.68 243.89 ± 170.52
Alb level (g/L) 40.03 ± 4.95 36.02 ± 6.08
BUN level (mmol/L) 4.16 ± 1.45 5.53 ± 3.39
D-dimer level (mg/L) 0.93 ± 0.83 3.30 ± 3.54
Na+ level (mmol/L) 140.55 ± 3.34 139.11 ± 4.46
LOS (d, median–IQR) 8 (6–11) 16 (15–19)
Alb, albumin; BUN, blood urea nitrogen; CRP, C-reactive protein; Hb, hemoglobin; IQR, interquartile range; L, lymphocyte count; LDH, lactate dehydrogenase; LOS, length of stay; N, neutrophil count; NLR, neutrophil-to-lymphocyte ratio; PLR, platelet-to-lymphocyte ratio; SCr, serum creatinine; WBC, white blood cell.

Patients usually presented with abdominal pain (86.5%), rectal bleeding (78.1%), diarrhea (61.2%), vomiting (25.8%), or constipation (4.2%). More than one-third of the patients (n = 112; 43.1%) had essential hypertension; other patient conditions included coronary heart disease (n = 58; 22.3%), cerebrovascular disease (n = 26; 10%), diabetes (n = 25; 9.6%), and a recent history of intestinal surgery (n = 18; 6.9%). A few patients had been treated with nonsteroidal anti-inflammatory drugs (NSAIDs) (n = 28; 10.8%), calcium channel blockers (n = 45; 17.3%), β-blockers (n = 20; 7.7%), or angiotensin receptor blockers (n = 41; 15.8%).

The progression of ischemia according to colonoscopy results is shown in Figure 2. Ischemic changes were found in the distal ileum (8.1%), ascending colon (10.4%), hepatic flexure (9.6%), transverse colon (23.5%), splenic flexure (27.7%), descending colon (52.3%), sigmoid colon (58.1%), and rectosigmoid junction (4.6%). In some patients, ischemia extended to more than 2 colon segments or even the entire colon. Young people were less susceptible to IC. A total of 9 young patients (<40 years old) with IC were enrolled in this study; 55% of them were men. Their mean age was 32 years (range, 24–38 years). Eight patients developed the disease in the left colon and one in the right colon, and all received symptomatic therapy.

Only 129 patients underwent computed tomography (CT) angiography of the superior mesenteric artery. Approximately 45.7% of these patients showed negative results, and the other patients showed different degrees of atherosclerosis, stenosis, or even embolism.

Prognostic nomogram

Univariate predictors of the prognosis of IC are shown in Table 1. After performing purposeful stepwise regression in the multivariate analysis, 6 predictors were obtained: neutrophil count > 6.3 × 109/L, D-dimer level ≥ 0.55 mg/L, ischemia of the distal ileum, ischemia of the hepatic flexure, ulceration, and luminal stenosis (Table 3). The model is presented as a nomogram in Figure 3. All variables were set as binary for easy calculation.

Table 3. - Multivariate logistic regression analysis of patients with ischemic colitis and poor disease prognoses
Variable OR (95% CI) P value
Neutrophil count >6.3 × 109/L 14.168 (4.986–40.264) <0.0001
D-dimer level ≥0.55 mg/L 47.206 (6.905–322.706) <0.0001
Distal ileum 25.464 (5.06–128.142) <0.0001
Hepatic flexure 29.9 (6.308–141.738) <0.0001
Ulceration 2.534 (1.073–5.984) 0.0339
Luminal stenosis 37.954 (10.518–136.95) <0.0001
CI, confidence interval; OR, odds ratio.

Figure 3.
Figure 3.:
A nomogram was constructed based on 6 clinical parameters. The length of the line segment corresponding to each variable reflects the contribution of this factor to the outcome. The points at the top of the graph represent the scores for each variable with different values. The total points represent the sum of the individual scores of all variables. The severe risk value corresponding to the total points is the probability of the occurrence of the event.

Validation and performance of the nomogram

The final logistic regression model had high overall accuracy for predicting the prognosis, with an AUROC of 0.86 (Table 4). In the external validation cohort, 26.8% (11/41) of the patients were defined as having poor prognoses. The model showed good discrimination ability during external validation, with an AUROC of 0.95, which was even better than the internal validation results. Regardless of the verification method used, the kappa coefficient was highly consistent with the predicted results of the model and the actual classification results.

Table 4. - Model performance parameters
Internal 5-fold cross-validation (n = 260) External validation (n = 41)
Sensitivity 84.52% 100%
Specificity 89.77% 97%
Correct rate 88.08% 98%
Youden index 0.7429 0.9677
AUC 0.8609 0.9545
Kappa coefficient 0.7316 (0.6434–0.8192) 0.9360 (0.8125–1.0000)
AUC, area under the curve.

Subgroup multivariate analysis

To further explore whether there were differences in prognostic predictors across age groups, subgroup analyses were performed by combining internal and external cohorts and separating them into patients older and younger than 65 years. The factors for poor prognoses were different between patients older than 65 years and younger than 65 years. More details are shown in Table 5 and Table 6.

Table 5. - Multivariate analysis of a subgroup of patients younger than 65 years
Variable Regression coefficient SE OR (95% CI) Wald χ2 P value
Intercept 5.71 1.53 13.85 0.0002
N ≤ 6.3 × 109/L −1.91 0.69 0.15 (0.04–0.58) 7.60 0.0058
NLR <5 −2.11 0.60 0.12 (0.04–0.39) 12.36 0.0004
D-dimer <0.55 mg/L −2.87 1.15 0.06 (0.01–0.54) 6.22 0.0126
Ascending colon 2.48 1.03 12.05 (1.58–90.91) 5.76 0.0164
HR ≤ 100 beats/min −2.34 0.97 0.10 (0.02–0.64) 5.83 0.0157
CI, confidence interval; HR, heart rate; N, neutrophil count; NLR, neutrophil-to-lymphocyte ratio; OR, odds ratio.

Table 6. - Multivariate analysis of a subgroup of patients aged 65 years and older
Variable Regression coefficient SE OR (95% CI) Wald χ2 P value
Intercept 7.27 1.62 20.27 <0.0001
N ≤ 6.3 × 109/L −2.01 0.48 0.134 (0.052–0.346) 17.33 <0.0001
D-dimer level <0.55 mg/L −4.1 1.23 0.02 (0.00–0.18) 11.17 0.0008
Distal ileum 2.12 0.92 8.33 (1.37–50.00) 5.30 0.0213
Hepatic flexure 2.64 0.92 14.08 (2.34–83.33) 8.34 0.0039
Splenic flexure 1.22 0.50 3.39 (1.27–9.09) 5.96 0.0146
Stenosis 1.31 0.57 3.70 (1.21–11.36) 5.28 0.0216
CI, confidence interval; N, neutrophil count; OR, odds ratio.

Similarly, to further compare the differences in prognosis between patients with left and right colon involvement, the 2 groups of patients with different outcomes were further divided into 3 subgroups. The grouping criteria for subgroup analysis were left colon, right colon, and both left and right colon. Multivariate analysis of the left colon subgroup showed that higher neutrophil count, higher D-dimer level, higher neutrophil-to-lymphocyte ratio (NLR), and colon stenosis were associated with poor prognoses (Table 7). However, because of the small number of patients in the other 2 groups, the model results could not be obtained.

Table 7. - Multivariate analysis of the left colon subgroup
Variable Regression coefficient SE OR (95% CI) Wald χ2 P value
Intercept 0.26 0.28 0.80 0.3714
N ≤ 6.3 × 109/L −1.40 0.43 0.25 (0.11–0.57) 10.65 0.0011
D-dimer level <0.55 mg/L −2.44 0.76 0.09 (0.02–0.39) 10.27 0.0013
NLR <5 −1.02 0.42 0.36 (0.16–0.82) 5.91 0.0151
Stenosis 1.12 0.44 3.06 (1.28–7.31) 6.33 0.0094
CI, confidence interval; NLR, neutrophil-to-lymphocyte ratio; OR, odds ratio.

DISCUSSION

Laboratory examination or colonoscopy alone was insufficient to adequately assess prognoses. A comprehensive predictive model can be used for the early, rapid, and quick assessment of prognosis. We developed such a model using retrospective, high-quality, and multicenter data. To facilitate practical use, the model was constructed using 2 laboratory variables and 4 variables observed during colonoscopy. We found that poor prognoses in patients aged 65 years and older were mainly related to the colonic ischemic site. Poor outcomes in patients younger than 65 years were mainly associated with abnormal laboratory indicators. The accuracy and reproducibility of the model were validated both internally and externally. To the best of our knowledge, currently, this model is the only one that has been validated internally and externally to predict poor prognoses in patients with IC.

An earlier study using a predictive model found that tachycardia, shock within 24 hours of admission, and ulcers found on endoscopy were independent predictors of poor prognoses. The probability and risk index for severe IC for patients with all 3 risk factors were 74-times higher than those for patients without risk factors (9). Sun et al. (10) identified the following possible predictors of poor prognoses: male sex, tachycardia, no rectal bleeding, peritonitis, hypotension (systolic blood pressure <90 mm Hg), and isolated right colonic ischemia. Pastor et al. (11) established a prognostic model combining ultrasonographic and clinical manifestations, including pain, diarrhea, rectal bleeding, hypertension, and pericolic fat changes. The evidence for these models is insufficient because of a lack of external validation. Moreover, it is difficult to compare mild and severe cases because of the different classification criteria of each model.

Partly in line with previous studies, we found evidence of ulceration and right colonic ischemia as predictors of poor prognosis. The difference is that the previous model did not include laboratory variables, which our study did. In addition to large sample size and a comprehensive collection of clinical data, most prognostic factors mentioned in previous studies were included in this study. However, evidence of endoscopic mucosal necrosis was not included in the model because necrosis is inherently an indicator of poor prognosis and the urgent need for surgery. This study shows that when the evidence of colonic necrosis is not clear, clinicians can use our model to determine which patients need more attention and strengthen treatment. We also designed dichotomous variables and a nomogram to facilitate the clinical application of the model. An easy-to-understand nomogram can be used to predict the risk of poor prognoses without memorizing the formula.

In this study, ischemic sites were identified based on detailed considerations. Consistent with previous studies (3,6,12), right colon ischemia was strongly associated with poor prognosis in this study. Evidence of ischemia in the terminal ileum and ascending colon was incorporated into the predictive model. Other studies have generally mentioned different signs and causes of left and right colon ischemia, but so far, we have not seen a prognostic model based on the location of ischemia. In our study, subgroup analysis of the patients with left colon involvement showed that neutrophil count, NLR, D-dimer level, and evidence of colon stenosis were all associated with poor prognoses. Right colon subgroup analysis was not possible because of the small number of patients.

Elderly patients are prone to IC, which is often accompanied by some primary diseases. Widely reported diseases associated with IC include cardiovascular and cerebrovascular diseases (such as coronary heart disease, arrhythmia, and stroke), hypertension, diabetes, infections (e.g., Escherichia coli and hepatitis B virus infections), pancreatitis, vasculitis, and irritable bowel syndrome (10,13). In a study of IC in young adults, 21% of patients younger than 40 years had a history of an autoimmune disease such as systemic lupus erythematosus or vasculitis (4). In our study, the incidence of comorbidities in elderly patients was similar to that previously reported (10,13). Among people younger than 40 years, the underlying diseases were chronic gastritis (n = 2), fatty liver (n = 2), and hepatitis B (n = 2). We did not find associations between these comorbidities and poor prognoses of IC.

The predisposing factors for IC reported in the literature include medications, colonoscopy, trauma, pancreatitis, hypovolemia, alcohol abuse, abdominal or aortic surgery, and long-distance running (14). The administration of an enema and colonoscopy performance may increase the pressure on the bowel, thus leading to bowel ischemia (5). Removal of a malignant tumor from the colon may reduce the blood supply to the surrounding intestine (15). Similarly, the occurrence of IC in some patients in our study was caused by definite causes: partial colon resection for colon cancer (n = 18), colonoscopy (n = 3), running (n = 1), and trauma (n = 1). However, there was no clear association between these triggers and poor prognoses.

The use of certain drugs has been an increasing focus of attention as a risk factor for IC. In the literature on pharmacological causes of colonic ischemia, psychotropic medications, NSAIDs, digitalis, agents that cause constipation or diarrhea, hormones, and tumor necrosis factor-alpha inhibitors had the strongest associations with IC (16). A national cohort study showed that β-blockers, opioids, and NSAIDs increase the risk of IC (17). In this study, the most commonly used drugs for patients before admission included NSAIDs, β-blockers, calcium channel blockers, and angiotensin receptor blockers. The univariate analysis showed that these drugs were not associated with the prognosis of IC. Opioids are tightly controlled in China and are only used for anesthesia and severe pain. None of the patients in this study took opioids, so its use is not comparable with that in other studies.

The severity and prognoses of IC have been associated with some laboratory variables. Some studies showed that patients with severe IC had elevated white blood cell counts, higher than normal blood urea nitrogen and lactate dehydrogenase levels, and lower albumin and hemoglobin levels (1,18,19). The univariate analysis in this study showed that patients with severe IC had lower albumin levels, lymphocyte count, serum sodium content, and higher levels of D-dimer, neutrophils, blood urea nitrogen, and C-reactive protein. In the end, only neutrophil count and D-dimer level were included in the prediction model. In the subgroup of patients younger than 65 years, heart rate > 100 beats per minute also suggested a poor prognosis.

The NLR and platelet-to-lymphocyte ratio have been widely used as readily available inflammatory indicators to assess the severity and prognoses of cardiovascular disease, cancer, and gastrointestinal disease (15,20–23). A high NLR has been shown to be an independent predictor of death from coronary artery disease, acute coronary syndrome, and congestive heart failure (23). During the univariate analysis, we found that the NLR was statistically significant when classified by multiple criteria (NLR ≥5/7/10) but that the platelet-to-lymphocyte ratio was only statistically significant when bound by a value of 120. None of them were included in our prognostic model. However, NLR ≥ 5 was statistically significant in the multivariate subgroup analysis for individuals younger than 65 years and with left colon involvement.

Ultrasonography is of limited value for imaging IC because gases in the hollow organs can interfere with the clinician's judgment. Changes in pericolic fat and colitis may indicate sonographic manifestations of severe colonic ischemia (11). CT findings of patients with IC may include deposition of mesenteric fat, thickening of the intestinal wall, and abnormal strengthening of the contrast of the intestinal wall; however, these findings were independent of disease severity (24). In this study, too few patients underwent abdominal ultrasonography and CT, so these data were not included. However, nearly half of the patients underwent CT angiography, and we found that patients with poor outcomes had more severe atherosclerosis, with only 17 patients having normal results.

This study also had some limitations. First, we did not collect follow-up data after discharge. Second, we noticed that decreases in hemoglobin and bicarbonate levels or increases in white blood cell or lactate dehydrogenase levels during hospitalization were frequently seen in patients with severe IC (1). However, changes in laboratory variables were not included in our prediction model. Owing to the limitations of the retrospective study, we were unable to perform any interventions. Many patients with good outcomes had undergone only one blood test, so we did not have laboratory parameters for all patients 48 hours after hospitalization and could not compare them further. Therefore, larger sample sizes and more detailed data on changes in laboratory variables during hospitalization are needed in the future to obtain more accurate models of future mortality projections.

In conclusion, we developed a nomogram-based prognostic model, based on a multicenter, retrospective, and real-world data, to evaluate predictors of poor prognoses in patients with IC. This model was confirmed to have good internal and external validity. This model can enable identification of patients with poor prognosis and those who will require long hospitalization time and excessive medical resources to allow for early intervention and avoid adverse consequences. The improvement of the model requires a larger sample size and more data on changes in variables during hospitalization.

CONFLICTS OF INTEREST

Guarantor of this article: Lan Zhong, MD.

Specific author contributions: Yiwei Luo, MM has equal rights with the first author Shan Li, MB, and Junyi Han, MD has equal rights with the corresponding author Lan Zhong, MD. Study concept and design: S.L. and L.Z. Acquisition of data: Y.L., W.W., and X.Y. Analysis and interpretation of data: S.L., J.L., M.H., J.H., and Q.S. Manuscript writing: S.L., J.L., Y.L., W.W., X.Y., M.H., Q.S., and L.Z. Analysis and interpretation of the data: X.Y. All authors approved the final draft submitted.

Financial support: This work was funded by Technology Development Project of Pudong Science, Technology and Economic Commission of Shanghai (Grant No. PKJ2017-Y17), Key Specialty Construction Project of Pudong Health and Family Planning Commission of Shanghai (Grant No. PWZzk2017--26) and The Top-Level Clinical Discipline Project of Shanghai Pudong (PWYgf2018-04). The authors received research funding in statistics and publishing.

Potential conflicts of interest: None to report.

Informed consent: Informed consent was obtained from all study participants.

Study Highlights

WHAT IS KNOWN

  • ✓ Severe ischemic colitis (IC) patients have higher recurrence and mortality rates than mild colitis patients.
  • ✓ There is no scoring model with both internal and external validation to predict poor outcomes.

WHAT IS NEW HERE

  • ✓ We developed a nomogram-based prognostic model for patients with IC.
  • ✓ Patients with ischemia in the hepatic flexure and distal ileum had a poor prognosis.
  • ✓ Patients with endoscopic evidence of ulcer or stenosis had a poor prognosis.
  • ✓ Patients with a higher blood neutrophil count and serum D-dimer level had a poor prognosis.
  • ✓ The poor prognosis of patients aged 65 years and older was related to the colonic ischemia site.
  • ✓ The poor prognosis of patients younger than 65 years was associated with abnormal laboratory indicators.

ACKNOWLEDGMENT

The authors thank Yibin Guo for his help with the statistical analysis.

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© 2021 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of The American College of Gastroenterology