University of Toledo Medical Center, Toledo, OH; Hackensack Meridian Health Palisades Medical Center, North Bergen, NJ; West Virginia University Health Sciences Center Charleston Division, WV; John H. Stroger Jr, Hospital of Cook Country, Chicago, IL; University of Utah, Salt Lake City, UT, USA
aDepartment of Medicine, University of Toledo Medical Center, Toledo, OH (Sachit Sharma, Christian Nehme, Muhammad Aziz, Ashu Acharya, Sami Ghazaleh); bDepartment of Medicine, Hackensack Meridian Health Palisades Medical Center, North Bergen, NJ (Simcha Weissman); cDepartment of Medicine, West Virginia University Health Sciences Center Charleston Division, Charleston, WV (Ahmad Khan); dDepartment of Medicine, John H. Stroger Jr, Hospital of Cook County, Chicago, IL (Ishaan Vohra); eDepartment of Gastroenterology, The University of Toledo Medical Center, Toledo, OH (Ali Nawras); fDepartment of Gastroenterology, University of Utah, Salt Lake City, UT (Douglas G. Adler), USA
Background The differences in outcomes between acute biliary pancreatitis (ABP) and acute alcohol-induced pancreatitis (AAP) have not been well studied. We sought to examine the differences between ABP and AAP as regards to in-hospital outcomes and resource utilization, using a large nationwide database.
Methods We queried the National Inpatient Sample databases 2016 and 2017 using the International Classification of Diseases, 10th revision, Clinical Modification (ICD-10-CM) coding system to identify the patients with a primary diagnosis of AAP and ABP. The primary outcome was all-cause in-hospital mortality. Secondary outcomes were hospital length of stay (LOS), hospitalization charge/cost, shock, acute kidney injury (AKI), intensive care unit (ICU) admission, and home discharge. Analysis was performed with STATA software.
Results There was no significant difference in mortality between patients with AAP and ABP (0.42% vs. 0.82%, adjusted odds ratio [aOR] 0.95, 95% confidence interval [CI] 0.69-1.31; P=0.79). Patients with ABP had a significantly longer LOS (+0.48 days, P<0.001). Patients with ABP had significantly higher adjusted mean hospitalization charges ($+19,958, P<0.001) and costs ($+4,848, P<0.001). Patients with ABP had a significantly lower likelihood of shock (aOR 0.75, 95%CI 0.59-0.95; P=0.02), AKI (aOR 0.76, 95%CI 0.71-0.82; P<0.001) or ICU admission (aOR 0.74, 95%CI 0.62-0.88; P=0.001). They were more likely to be discharged home (aOR 1.26, 95%CI 1.18-1.34; P<0.001).
Conclusion Although there was no difference in all-cause mortality, patients with ABP had better hospitalization outcomes but greater resource utilization.
Keywords Acute biliary pancreatitis, acute alcohol-induced pancreatitis, mortality, outcomes, resource utilization
Acute pancreatitis (AP) is an acute inflammatory process involving the pancreas with considerable morbidity and mortality [1]. Global incidence is estimated to be about 34 cases per 100,000 population per year, with no significant sex-related differences [2]. The prevalence of AP has more than doubled in recent years, and AP is considered one of the most common gastrointestinal cause for hospitalization in the United States (US) [3]. AP poses a significant economic burden on the US healthcare system, with more than $10 billion in estimated costs annually, and this trend is increasing [4,5].
The most common cause of AP is biliary stone disease (choledocholithiasis) followed by alcohol-induced pancreatitis. Together, they account for almost 70-80% of all cases of AP [6-8]. Other causes of AP include post-endoscopic retrograde cholangiopancreatography pancreatitis, medications, hypertriglyceridemia, hypercalcemia, trauma, infections, autoimmune, genetic, and idiopathic [7]. When comparing outcome differences between 2 different etiologies of AP, acute alcohol-induced pancreatitis (AAP) and acute biliary pancreatitis (ABP), some studies have reported a more severe outcome among patients with ABP [9,10], while other studies have reported a more severe course and higher mortality in patients with AAP [11,12]. Other studies have reported no difference in mortality between the 2 groups [8,13].
We performed a retrospective analysis of the Nationwide Inpatient Sample (NIS) to compare the clinical course and outcomes between patients with AAP and ABP.
We queried the Healthcare Cost and Utilization Project (HCUP) NIS database for the years 2016 and 2017. The NIS is a database of inpatient hospital stays in the United States (excluding rehabilitation and long-term acute care hospitals) derived from billing data submitted (by hospitals) to statewide organizations based off discharge abstracts. The NIS 2016 database contains data from 7.1 million hospital stays in 4575 hospitals in 47 US states, while the NIS 2017 database contains data from 7.1 million hospital stays in 4584 hospitals in 48 US states [14]. It contains de-identified clinical and nonclinical elements at both the patient and hospital level using the International Classification of Diseases, 10th revision, Clinical Modification (ICD-10-CM) coding system. The current study was performed using the ICD-10-CM codes, which are more specific than the previous iteration, in place prior to the years examined [15]. NIS 2017 has an increased number of secondary diagnoses (29-39) and inpatient procedures (15-25), which allowed us to generate a more comprehensive list of patients and procedures than the previous NIS databases.
We used the ICD-10-CM codes to identify the following: (a) patients admitted with a primary diagnosis of AP; and (b) patients admitted with a primary diagnosis of AAP or ABP. Patients were excluded if they were <18 years old or if they had elective admission. The ICD-10-CM diagnostic and procedural codes used in this study are presented in the Supplementary Table 1. Inclusion and exclusion criteria are shown in the flow diagram (Fig. 1). This study was deemed exempt from institutional review board approval at the University of Toledo, as it was performed using de-identified and publicly available data.
Figure 1 Patient selection flow diagram
AP, acute pancreatitis
Patient demographics collected included: age, sex, race (Caucasian, Black, Hispanic, Asian, Pacific Islander, Native American, and other), median household income (based on patient’s zip code), primary expected payer (Medicare, Medicaid, private insurance, and uninsured), hospital size (small, medium, and large) in terms of number of beds, hospital teaching status, hospital region (Northeast, Midwest, South, and West), and urban location. The burden of comorbidities was assessed using the Charlson comorbidity index. Mortality rate, patient discharge, hospital length of stay (LOS), total charges (the amount billed by the hospital for the rendered services), as well as the (actual) cost of care were all obtained directly from the NIS. Total hospitalization charge is the amount billed to the patient and is directly available in the NIS, but is different from hospitalization cost, which is the actual cost incurred by the hospital in treating the patient [16,17]. A cost-to-charge ratio is available from HCUP and can be used to calculate the hospitalization cost [18].
The primary outcome was in-hospital all-cause mortality. Secondary outcomes were: (a) mean LOS; (b) mean hospitalization charges and costs; (c) shock; (d) sepsis; (e) acute kidney injury (AKI); (f) intensive care unit (ICU) admission; (g) likelihood of pancreatic drainage; and (h) likelihood of discharge to home. All these outcomes were defined using standard ICD-10-CM diagnostic and procedural codes, as shown in the Supplementary Table 1.
Statistical analysis was performed using STATA, version 16.0 (StataCorp., College Station, Texas, US). This software facilitates analysis to produce nationally representative unbiased results, variance estimates and P-values. Weighting of patient-level observations was implemented. NIS contains a 20% sample of all hospitals within each stratum. During analysis, this sample was weighted (weight = total number of discharges from all acute care hospitals in the US divided by the number of discharges included in the 20% sample) to obtain nationally representative data [19]. Multivariate regression analysis was used to adjust for potential confounders. Univariate analysis was initially performed to calculate the unadjusted odds ratio (OR) and determine confounders significantly associated with the outcomes. Significant association was determined as a cutoff P-value of 0.2. A multivariate regression model was then constructed, including all confounders found to be significant by univariate analysis—age, sex, race, comorbidity score, insurance status, hospital region, hospital location, income quartile, congestive heart failure (CHF), cirrhosis, chronic kidney disease (CKD), end-stage renal disease (ESRD), diabetes mellitus (DM), obesity—to calculate the adjusted OR (aOR). Logistic regression was used for binary outcomes and linear regression was used for continuous outcomes. Proportions were compared using the chi-square test and continuous variables were compared using the Student’s
A total of 585,579 adult patient admissions were identified with a diagnosis of AP during hospitalization in 2016 and 2017. Patients under the age of 18 years (10,350) and with elective admission (21,749) were excluded from the study, leaving 553,480 adult patients admitted with AP. Mean age was 51.8 years, and most of the patients were male (53.22%). Private insurance was the patients’ primary payer (33.16%), followed by Medicare (31.92%). The majority of patients were white (64.23%). Patients were predominantly admitted to teaching hospitals (60.52%). Just over one quarter (25.3%) of the patients had AAP and 17.44% patients had ABP (Fig. 2). The complete patient and hospital characteristics are presented in Tables 1 and 2, and the outcomes are presented in Table 3.
Figure 2 Etiology of acute pancreatitis in our National Inpatient Sample study
Table 1 Characteristics of patients admitted to hospital with acute pancreatitis
Table 2 Characteristics of patients admitted with acute pancreatitis in hospital: acute biliary pancreatitis (ABP) versus acute alcohol-induced pancreatitis (AAP)
Table 3 Outcomes in patients with acute pancreatitis: acute biliary pancreatitis (ABP) vs. acute alcohol-induced pancreatitis (AAP)
Patients with ABP were more likely to be female compared to patients with AAP (59.4% vs. 30.73%, P<0.001), and were older (57.03 vs. 45.31 years, P<0.001). Patients with ABP had a higher prevalence of CHF (7.76% vs. 2.75%, P<0.001), type 2 DM (22.37% vs. 13.11%, P<0.001), CKD (10.19% vs. 3.25%, P<0.001), ESRD (1.61% vs. 0.34%, P<0.001), and obesity (26.26% vs. 8.24%, P<0.001). Patients with AAP had a higher prevalence of liver cirrhosis (5.55% vs. 2.5%, P<0.001) and smoking (66.17% vs. 30.75%, P<0.001). Patients with AAP had a higher prevalence of pancreatic necrosis (2.62% vs. 1.97%), but this difference was not significant on multivariate analysis (aOR 0.89, 95% confidence interval [CI] 0.76-1.05; P=0.19).
The total all-cause in-hospital mortality in patients with AP was 0.59% (3285 of 553,480 patients). The total mortality was 0.42% (595 of 140,195 patients) among patients with AAP and 0.82% (800 of 96,540 patients) among patients with ABP. On multivariate analysis, there was no significant difference in all cause in-hospital mortality between patients with AAP and those with ABP (aOR 0.95, 95%CI 0.69-1.31; P=0.79).
The mean LOS among patients admitted with AP was 4.3 days. Mean LOS was 4.38 days (95%CI 4.32-4.44) in patients with AAP and 5.1 days (95%CI 5.01-5.18) in patients with ABP. After adjusting for confounders using multivariate regression analysis, patients with ABP had a significantly longer mean LOS compared to patients with AAP (+0.48 days, P<0.001).
The mean hospitalization charges and cost for patients admitted with AP were $41,018 and $10,153, respectively. Patients with ABP had significantly higher adjusted mean total hospitalization charges and costs ($61,182 and $14,941) compared to patients with AAP ($37,982 and $9,583). The mean adjusted difference in hospitalization charges was $+19,958 (P<0.001), and the mean adjusted difference in hospitalization costs was $+4,848 (P<0.001).
Among all patients with AP, 0.83% developed shock during their hospital stay. The proportion of patients developing shock was 0.96% in AAP and 1.06% in ABP. Although the difference was small, patients with ABP had a significantly lower likelihood of shock compared to patients with AAP (aOR 0.75, 95%CI 0.59-0.95; P=0.02).
Among all patients with AP, 3.2% developed sepsis during their hospital stay. The proportion of patients developing sepsis was 3.97% in AAP and 3.35% in ABP. There was no significant difference in the likelihood of sepsis between these groups (aOR 0.90, 95%CI 0.80-1.01; P=0.10).
Among all patients with AP, 10.98% developed AKI during their hospital stay. The proportion of patients developing AKI was 10.34% in AAP and 11.54% in ABP. Patients with ABP were significantly less likely to have AKI compared to patients with AAP (aOR 0.76, 95%CI 0.71-0.82; P<0.001).
Among all patients with AP, 1.35% patients needed ICU admission during their hospital stay. The proportion of patients needing an ICU stay was 1.96% in AAP and 1.71% in ABP. Patients with ABP were significantly less likely to be admitted to the ICU compared to patients with AAP (aOR 0.74, 95%CI 0.62-0.88; P=0.001).
Overall, 0.60% of patients with AP underwent pancreatic drainage; 0.42% of patients with AAP underwent pancreatic drainage as compared to 0.45% of patients with ABP. On multivariate analysis, there was no significant difference in the likelihood of pancreatic drainage in these groups (aOR 1.15, 95%CI 0.81-1.62; P=0.42).
A total of 466,744 (87.49%) patients with AP were discharged home after the hospitalization; 86.12% of patients with AAP and 83.39% of patients with ABP were discharged home. On multivariate analysis, patients with ABP were more likely to be discharged home than patients with AAP (aOR 1.26, 95%CI 1.18-1.34; P<0.001).
Our retrospective analysis of the NIS database showed that there was no significant difference in all-cause in-hospital mortality between patients with AAP and ABP. Patients with ABP had a longer LOS, higher hospitalization charges/costs, and a significantly smaller likelihood of shock, AKI, and ICU admission. However, it is pertinent to remember that, while statistically significant, the differences in some of these outcomes were quite modest and indicate a somewhat similar clinical course between the 2 groups. There have been previous studies comparing the outcomes of alcohol-induced and gallstone pancreatitis in patients admitted to tertiary centers, but the sample size was in the hundreds [20,21]. In comparison, we were able to look at 553,480 adult patients with AP across the nation, including 140,195 (25.3%) with AAP and 96,540 (17.44%) with ABP.
Previous studies have shown a correlation between sex and the etiology of AP, with a higher percentage of male patients having AAP and a higher percentage of females having ABP [8,22]. Furthermore, patients with AAP were found to be younger than those with ABP [8]. Our study shows similar results: patients with ABP were more likely to be female (59.4% vs. 30.73%, P<0.001) and older (57.03 vs. 45.31 years, P<0.001) compared to patients with AAP. This is consistent with the current evidence that biliary stone disease is almost twice as likely in females than in males, and that age has a positive correlation with the frequency of the disease [23]. In addition, patients with ABP were found to have a significantly higher prevalence of CHF, Type 2 DM, CKD, ESRD, and obesity, while patients with AAP had significantly more liver cirrhosis and were more likely to be smokers.
In our study, there was no significant difference in all-cause in-hospital mortality between patients with AAP and ABP (aOR 0.95, 95%CI 0.69-1.31; P=0.79). Multiple studies have reported a similar absence of mortality difference between the 2 groups [8,13,20]. However, some studies reported a more severe course and higher mortality in the alcohol group [11,12], while other, older studies reported a more severe outcome in the biliary group [9,10].
We found that a higher percentage of patients with AAP had pancreatic necrosis compared to ABP (2.62% vs. 1.97%, P<0.001), but the difference was not significant on multivariate analysis. There was no significant difference in infected necrosis between the 2 groups. Samanta
Patients with ABP also had a longer LOS and higher hospitalization charges and costs compared to the patients with AAP. This is not surprising, as patients with ABP are more likely to undergo imaging studies, including magnetic resonance cholangiopancreatography, and endoscopic procedures, such as ERCP, that can add to the overall LOS and costs. However, the difference in LOS between the 2 groups was less than 12 h (0.48 days), and its clinical relevance is debatable. A recent database study of patients with ABP showed that the hospitalization cost was increasing, even though use of ERCP in ABP patients was decreasing [26].
Our study has multiple limitations. Our data were obtained using NIS, an administrative, claim-based database. It has been previously documented that missing or inaccurately entered codes are part of claim-based databases such as NIS. We only included patients with a primary diagnosis (DX1) of acute pancreatitis to increase the specificity of our study. In doing so, some of the other pertinent clinical variables coded as secondary diagnoses (DX2-40) may have been missed. As shown by Xiao
As discussed above, there is significant heterogeneity in the evidence regarding a difference in outcomes of AP based on etiology [21,28-31]. Furthermore, there is a paucity of data on the outcome differences between the most common types: AAP and ABP. The major strength of our study is that it compares the outcomes of 553,480 patients with AP across the nation, while focusing on in-hospital outcomes of alcohol-induced and biliary acute pancreatitis. This large sample size minimizes the likelihood of a β error. The results of our study are also representative of real-life practice in US hospitals, and can thus be generalized to the US population. Hence, our study helps to bridge the gap in this knowledge.
In conclusion, our study showed no difference in mortality when comparing patients with AAP and ABP. When looking at resource utilization, patients with ABP had a longer LOS and higher hospitalization charges and costs compared to patients with AAP. Patients with ABP were less likely to develop shock, AKI, or be admitted to the ICU when compared to patients with AAP and they were also more likely to be discharged home. While statistically significant, the differences between several of these outcomes were small and the limitations of this study should be kept in mind when interpreting the results. Nevertheless, clinicians should be wary of these potential adverse outcomes in patients with AAP, and care should be focused on close hemodynamic and electrolyte monitoring for the earlier detection and prevention of these comorbidities. Further prospective studies and meta-analysis will help successfully guide clinical practice in the future.
What is already known:
Acute pancreatitis (AP) is the most common cause of gastroenterological admission, with alcohol-induced and biliary pathology being the most common etiologies
Acute alcohol-induced pancreatitis (AAP) and acute biliary pancreatitis (ABP) are 2 distinct entities with different causes, pathogenesis, and clinical course
There is still significant heterogeneity regarding differences in the outcomes of AP based on etiology, primarily AAP vs. ABP
What the new findings are:
In the National Inpatient Sample discharge database based on ICD-10 coding, AAP and ABP make up less than 50% of all causes of AP
There is no difference in in-hospital mortality rates between AAP and ABP
Compared to AAP, patients with ABP do better in terms of other in-hospital outcomes such as shock, acute kidney injury and intensive care unit admission, and incur lower hospitalization costs, to a small but statistically significant degree
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