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Gastroenterology

Risk Factors of Gastrointestinal Perforation with a Poor Prognosis

, , , , &
Pages 4637-4647 | Received 19 Jun 2023, Accepted 09 Oct 2023, Published online: 16 Oct 2023

Abstract

Background

Despite medical progress, mortality from gastrointestinal perforation was relatively high. Our study’s objective was to identify risk factors associated with a poor prognosis for gastrointestinal perforation.

Methods

Patients diagnosed with gastrointestinal perforation at the Longchuan County People’s Hospital between January 2019 and February 2022 were the subject of a retrospective analysis of their laboratory data. Patients were grouped based on length of hospital stay, septic shock, and mortality.

Results

A total of 240 patients participated in our study. Using univariate and multivariate analysis, we identified several risk factors for gastrointestinal perforation associated with a dismal prognosis. Lower digestive tract perforation (OR=2.418, 95% CI 1.119–5.227, P=0.025), low total protein (OR=0.934, 95% CI 0.879–0.992, P=0.026) and low hemoglobin (OR=0.985, 95% CI 0.971–0.999, P=0.039) were linked to a longer length of stay, especially hemoglobin (OR=0.978, 95% CI 0.966–0.991, P=0.001) in upper digestive tract. High ratio of neutrophils to lymphocytes (NLR) (OR=1.043, 95% CI 1.012–1.076, P=0.007), high lymphocyte-to-monocyte ratio (LMR) (OR=2.158, 95% CI 1.495–3.115, P<0.001) and low prognostic nutrition index (PNI) (OR=0.814, 95% CI 0.751–0.833, P<0.001) predicted septic shock. In upper digestive tract, PLR (OR=1.001, 95% CI 1.000–1.002, P=0.067), LMR (OR=2.160, 95% CI 1.440–3.240, P<0.001) and PNI (OR=0.843, 95% CI 0.767–0.926, P<0.001) were risk factors for septic shock, and total protein (OR=0.796, 95% CI 0.686–0.923, P=0.003) was a risk factor for septic shock in lower digestive tract. High NLR (OR=1.056, 95% CI 1.019–1.093, P=0.003), high LMR (OR=1.760, 95% CI 1.177–2.632, P=0.006) and low PNI (OR=0.832, 95% CI 0.754–0.918, P<0.001) were the risk factors of mortality. In subgroup analysis of perforation site, albumin (OR=0.820, 95% CI 0.719–0.934, P=0.003) and LMR (OR=1.506, 95% CI 1.069–2.123, P=0.019) were risk factors for mortality in upper digestive tract and PNI (OR=0.636, 95% CI 0.445–0.908, P=0.013) was a risk factor for mortality in lower digestive tract.

Conclusion

Our research found that the perforation site, total protein, albumin, hemoglobin, NLR, LMR, PLR and PNI were risk factors for gastrointestinal perforation with a poor prognosis.

Introduction

Gastrointestinal perforation is the complete penetration of the digestive tract, which may be caused by inflammation,Citation1 ulcer,Citation2 medication,Citation3 diverticulum,Citation4 connective tissue disorders, neoplasm,Citation5 iatrogenic procedureCitation6 and so on. Leakage of alimentary contents into the peritoneal cavity may result in peritoneal infection, sepsis, septic shock, and even life-threatening complications following gastrointestinal perforation. Despite advances in surgery and emergency medicine, gastrointestinal perforation has a 10% to 50% mortality rate.Citation7–10 Acute abdominal pain may be the most frequent clinical manifestation of gastrointestinal perforation. However, some perforations, particularly colonic perforations, may progress slowly, delaying the initiation of appropriate treatment. Timely recognition of gastrointestinal perforation, particularly in cases with a poor prognosis, is crucial for reducing complications and mortality.

Some studies have identified risk factors for severe gastrointestinal perforation, such as aging, diabetes, and the use of nonsteroidal anti-inflammatory drugs or glucocorticoids.Citation11–13 Numerous studies have linked inflammatory response and nutritional status to the prognosis of gastrointestinal perforation. Aydin O demonstrated that platelet-to-lymphocyte ratio (PLR) and neutrophil-to-lymphocyte ratio (NLR) were positively associated with peptic ulcer perforation mortality, whereas lymphocyte count values were negatively associated with peptic ulcer perforation mortality.Citation14 In Mller MH’s meta-analysis, a low albumin level was positively associated with peptic ulcer perforation mortality.Citation15 Recent research has focused on the relationships between systemic inflammation and nutrition parameters, such as the systemic immune-inflammation index (SII), prognostic nutritional index (PNI), and hemoglobin, albumin, lymphocyte, and platelet (HALP) scores. They were calculated with the formula as follow.

Liu found SII outperformed NLR and PLR in predicting severe acute pancreatitis.Citation16 In Jiang’s systematic review, decreased PNI was associated with poor oesophageal cancer overall survival.Citation17 In acute pancreatitis with a high PNI, Akkuzu’s study found no local complications or fatalities.Citation18 High HALP score was associated with improved survival in several carcinomas, including colorectal cancer,Citation19 small cell lung cancer,Citation20 renal cell carcinoma,Citation21 and so on. However, SII, PNI, and HALP scores were not utilized in studies of gastrointestinal perforation. We reviewed patients with gastrointestinal perforation to identify risk factors of poor prognosis with common laboratory data and combined parameters related to inflammatory and nutritional status, which may be useful to primary hospital practitioners. Ours was the first study to investigate the relationship between SII, PNI, and HALP score and poor prognosis in gastrointestinal perforation.

Materials and Methods

Patients with gastrointestinal perforation admitted to Longchuan County People’s Hospital between January 2019 and February 2022 were identified. Such demographic data as age and gender were recorded. Laboratory data, including total protein, albumin, and routine blood test were reviewed. In addition, the location of the perforation, length of stay, septic shock, and prognosis for survival were recorded. Patients were divided into two groups based on length of hospital stay, incidence of septic shock, and mortality. Written informed consent was obtained from all the participants prior to the enrollment of this study. Our study was also approved by our institutional review board (Longchuan County People’s Hospital) and conducted in accordance with the Declaration of Helsinki’s principles.

Using SPSS 25.0 and Stata/SE 12.0, statistical analysis was conducted. Frequency (n/N) and percent (%) were used to express discrete variables. Continuous variables were expressed as median and quartile for nonparametric data or as mean ± standard deviation for data with a normal distribution. We analyzed univariate relationships with the Fisher’s exact test for categorical data, the Mann–Whitney U-test for nonparametric data, and the Student’s t-test for data with a normal distribution, selecting those parameters P < 0.1 for multivariate analysis. In the multivariate analysis, logistic regression analysis was used to identify independent risk factors for gastrointestinal perforation in terms of length of hospital stay, septic shock, and survival prognosis, and then a nomogram was generated. Using the receiver operator characteristic (ROC) curve, the C-index of the nomogram was calculated. The significance level was defined as a P value of <0.05.

Results

Patients

The study included 240 patients with gastrointestinal perforation. Among them, 180 patients were male. There were 185 patients diagnosed with upper gastrointestinal perforation, 51 with lower gastrointestinal perforation, and 4 with unknown perforation site. The average age of patients involved was 63.5 years old. The range of length of stay was from 0 to 59 days, with a mean of 9 days. Twenty-six patients experienced septic shock, and 21 patients’ dead eventually.

Risk Factors for Prolonged Length of Stay

A hospitalization was deemed to be prolonged if it was longer than or equal to the median length of stay. displays patients’ information associated with length of stay.

Table 1 Included Patients’ Information Divided According to Length of Stay

Univariate analyses identified variables with a potential independent correlation with prolonged length of stay and revealed that sex (P=0.043), the site of perforation (P=0.026), total protein (P=0.001), albumin (P=0.004), and hemoglobin (P=0.001) were associated with prolonged length of stay. Multivariate regression analyses including factors P<0.1 at univariate analyses and the significant clinical factor PLR disregarding P>0.1 at univariate analyses revealed that lower digestive tract, low total protein, and low hemoglobin were risk factors for prolonged length of stay, with OR values of 2.418 (95% CI 1.119–5.227, P=0.025), 0.934 (95% CI 0.879–0.992, P=0.026) and 0.985 (95% CI 0.971–0.999, P=0.039). depicts the risk factor nomogram of length of stay for patients with gastrointestinal perforation. depicts the ROC curve for discriminating length of stay, with a C-index of 0.693.

Figure 1 Nomogram of prolonged length of stay.

Figure 1 Nomogram of prolonged length of stay.

Figure 2 The ROC curve of length of stay.

Figure 2 The ROC curve of length of stay.

In subgroup analysis of perforation site, hemoglobin was a risk factor for prolonged length of stay in upper digestive tract, with OR values of 0.978 (95% CI 0.966–0.991, P=0.001). There was not risk factor for prolonged length of stay in lower digestive tract.

Risk Factors for Septic Shock

depicts patients’ information associated with septic shock.

Table 2 Included Patients’ Information Classified by Septic Shock

Univariate analyses identified variables with a potential independent correlation with septic shock and identified sex (P<0.001), age (P<0.001), total protein (P<0.001), albumin (P<0.001), neutrophils (P=0.025), lymphocyte (P=0.003), basophils (P=0.004), monocyte (P=0.001), hemoglobin (P<0.001), PLR (P=0.039), PNI (P=0.001) and HALP score (P=0.004) as these variables. Multivariate regression analyses including factors P<0.1 at univariate analyses and the significant clinical factor NLR and LMR disregarding P>0.1 at univariate analyses revealed that high NLR, high LMR, and low PNI were risk factors for septic shock, with OR values of 1.043 (95% CI 1.012–1.076, P=0.007), 2.158 (95% CI 1.495–3.115, P<0.001) and 0.814 (95% CI 0.751–0.833, P<0.001). depicts the risk factors nomogram of septic shock for patients with gastrointestinal perforation. depicts the ROC curve for discriminating septic shock, with a C-index of 0.845.

Figure 3 Nomogram representing septic shock.

Figure 3 Nomogram representing septic shock.

Figure 4 The ROC curve for septic shock discrimination.

Figure 4 The ROC curve for septic shock discrimination.

In subgroup analysis of perforation site, PLR, LMR and PNI were risk factors for septic shock in upper digestive tract, with OR values of 1.001 (95% CI 1.000–1.002, P=0.067), 2.160 (95% CI 1.440–3.240, P<0.001) and 0.843 (95% CI 0.767–0.926, P<0.001). In lower digestive tract, total protein was a risk factor for septic shock, with OR values of 0.796 (95% CI 0.686–0.923, P=0.003).

Risk Factors for Mortality

Patients information associated with mortality is depicted in .

Table 3 Included Patients’ Information Divided According to Mortality

Variables with a potential independent correlation with mortality were identified by univariate analyses, indicating total protein (P=0.001), albumin (P<0.001), lymphocyte (P=0.008), monocyte (P=0.019), hemoglobin (P=0.033) and PNI (P=0.001). Multivariate regression analyses including factors P<0.1 at univariate analyses and the significant clinical factor NLR, PLR, and LMR disregarding P>0.1 at univariate analyses revealed that NLR, LMR, and PNI were the risk factors of mortality, with OR values of 1.056 (95% CI 1.019–1.093, P=0.003), 1.760 (95% CI 1.177–2.632, P=0.006) and 0.832 (95% CI 0.754–0.918, P<0.001), respectively. The mortality nomogram for patients with gastrointestinal perforation is shown in . The ROC curve for distinguishing mortality is plotted in , and the C-index was 0.858.

Figure 5 Nomogram of mortality.

Figure 5 Nomogram of mortality.

Figure 6 The ROC curve for discriminating mortality.

Figure 6 The ROC curve for discriminating mortality.

In subgroup analysis of perforation site, albumin and LMR were risk factors for mortality in upper digestive tract, with OR values of 0.820 (95% CI 0.719–0.934, P=0.003) and 1.506 (95% CI 1.069–2.123, P=0.019). In lower digestive tract, PNI was a risk factor for mortality, with OR values of 0.636 (95% CI 0.445–0.908, P=0.013).

Discussion

Acute gastrointestinal perforation is associated with a high mortality rate. It is crucial to identify severe gastrointestinal perforations with a poor prognosis. To evaluate the mortality of critically ill patients, scoring systems such as Acute Physiology And Chronic Health Evaluation II (APACHE II) and Simplified Acute Physiology Score (SAPS II) exist. However, it is disease-independent. The Mannheim peritonitis index (MPI) is comprised of clinical information to evaluate outcome of peritonitis.Citation22 In our study, we identified several common blood indices that aid in the diagnosis of severe gastrointestinal perforation.

There were few studies that examined the length of hospital stay for patients with gastrointestinal perforation. In Kayano’s study, hospitalization duration was shorter in the high psoas muscle index (PMI) group than in the low PMI group.Citation23 As a nutrient storage system, muscles utilized amino acids to combat inflammation during a bacterial invasion. Similar to Kayano’s study, but with different nutrient indices for total protein and hemoglobin, our outcome was comparable. Low levels of total protein and hemoglobin were associated with an extended length of stay, especially low hemoglobin in upper digestive tract perforation. It was widely acknowledged that malnutrition suppressed immune function, which may result in severe infection and protracted hospitalization.Citation24,Citation25 Anemic patients frequently coexisted with malnutrition, cancer, and other chronic conditions, and had longer hospital stays.Citation26 Wang discovered that the group with an upper gastrointestinal tract had a longer length of stay than the group with a lower gastrointestinal tract,Citation27 while our outcome was contrary. In Wang’s study, it may have been caused by more severe conditions in the intensive care unit, whereas the majority of our patients were treated in the general ward. And only 33 patients participated in Wang’s study. In addition, there was no significant difference in septic shock between upper and lower gastrointestinal perforation in our study. In Wang’s study, however, the use of norepinephrine was more in upper gastrointestinal perforation than in lower gastrointestinal perforation, which may have contributed to longer hospitalization duration. The OR value of NLR was 0.970 (95% CI 0.939–1.002, P=0.065) in our study, which implied NLR maybe another risk factor of prolonged length of stay. Increased inflammation was associated with severe infection, extending the length of treatment. In COVID-19, a low PNI was associated with hospitalization lengthening.Citation28 SII played a significant role in predicting the length of stay in spinal deformity in adults.Citation29 There was no research examining the correlation between HALP score and length of hospital stay. In our univariate analyses, a P<0.1 correlation between low PNI and length of stay was observed. However, the OR values were 1.043 (95% CI 0.921–1.182, P=0.506) in multivariate regression analyses. In univariate analyses, the SII and HALP score P values were 0.436 and 0.163, respectively. In our study, PNI, SII, and HALP scores were not risk factors for length of stay in patients with gastrointestinal perforation.

Perforation of the gastrointestinal tract may cause septic shock. In patients with gastrointestinal perforation, CRP and PCT were independent risk factors for septic shock according to Chen’s warning scoring system.Citation30 Zhou discovered an association between increased SOFA score and sepsis of gastrointestinal perforation.Citation31 High NLR, high LMR, and low PNI were identified as risk factors for septic shock in our study. CRP, PCT, NLR, and LMR were common inflammatory response indices. Increased inflammation was closely associated with an immune response that was out of control, which may result in septic shock. Based on the physiological relationship between neutrophilia, lymphopenia, and mononucleosis in systemic inflammation, NLR and LMR were more sensitive than single white blood cell count.Citation32 In subgroup analysis, there were inflammatory response indices PLR and LMR detected significantly in upper digestive tract but not lower digestive tract. It might be due to lower digestive tract perforation tended to be inflammatory and upper digestive tract varied in inflammation. Severe inflammation was related to septic shock in upper digestive tract perforation. Nutritional reserve was essential for defending against bacterial invasion, and patients with low PNI and total protein were susceptible to septic shock. Li also demonstrated that neonatal PNI decreased with increasing severity of sepsis.Citation33 P<0.05 indicated a correlation between HALP score and septic shock in our univariate analyses, but the OR values were 1.013 (95% CI 0.933–1.099, P=0.764) in multivariate regression analyses. Other HALP score studies focused on carcinoma and did not include sepsis. Pricop suggested SII for sepsis prediction in odontogenic infection.Citation34 In Ma’s study, high-level SII sepsis patients tended to develop septic shock.Citation35 In our study, the P value of SII in univariate analyses was 0.277. In our study, neither SII nor HALP score was associated with septic shock in patients with gastrointestinal perforation.

The mortality rate associated with gastrointestinal perforation was relatively high. In Shimoyama’s study, NLR and PLR were independently linked to gastrointestinal perforation mortality.Citation32 We also discovered that high levels of the inflammatory factors NLR and LMR increased the mortality associated with gastrointestinal perforation, especially in upper digestive tract. As stated previously, uncontrolled inflammatory response led to the destruction of tissue and even death. In a study involving 146 patients with colorectal perforation, Matsuoka T. found a correlation between decreased albumin level and mortality.Citation36 Typically, serum albumin was used to assess nutritional status. In inflammatory responses, hypoalbuminosis frequently foretold a dismal prognosis. The PNI, a combination of albumin and lymphocytes, was associated with mortality from gastrointestinal perforation, according to our findings. In Wang’s study, hepatocellular carcinoma patients with high PNI and low SII had longer recurrence-free survival and overall survival.Citation37 In univariate analyses, however, SII was not a significant predictor of survival in our patients with gastrointestinal perforation with P value >0.1. Low HALP score was associated with decreased survival in patients with solid tumors, according to a meta-analysis by Xu.Citation38 In our study, a P<0.1 correlation between HALP score and mortality was observed in univariate analyses, but the OR values were 1.050 (95% CI 0.945–1.166, P=0.364) in multivariate regression analyses. In our study, SII and HALP scores were weak predictors of poor gastrointestinal perforation.

There were a few limitations to our research. Firstly, the study was conducted at a single location. Secondly, because our study was retrospective, it was challenging to obtain missing information such as other inflammatory markers, method of perforation and co-morbidities. Then, because the mean age of the included patients was over 60 years, our study was not representative. Lastly, there were insufficient patients for subgroup analysis of perforation site, which leaded to different results especially in lower digestive tract. In the future, we will conduct a large-scale, multi-center study to confirm our findings.

In conclusion, the perforation site, total protein, albumin, hemoglobin, NLR, LMR, PLR and PNI were poor prognostic factors for gastrointestinal perforation. In practice, we could assign significance to these parameters in order to distinguish perforations of the gastrointestinal tract with a poor prognosis.

Disclosure

The authors report no conflicts of interest in the work.

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