Literature DB >> 32362963

Outcomes of Clostridioides difficile Infection in Patients With Liver Cirrhosis: A Nationwide Study.

Abubaker O Abdalla1, Sailaja Pisipati2, Mohamed Elnaggar2, Mohit Rishi2, Rajkumar Doshi2, Nageshwara Gullapalli2.   

Abstract

BACKGROUND: Clostridioides difficile infection (CDI) is a major health problem that has been on the rise for the last couple of decades. It has significant mortality and morbidity in hospitalized patients. We looked at the outcomes of CDI in patients with liver cirrhosis compared to those without liver cirrhosis.
METHODS: We conducted a retrospective study from a large inpatient database. The National Inpatient Sample (NIS) was queried for CDI admissions between January 2012 and September 2015. Patients admitted with CDI were identified using the International Classification of Diseases, Ninth Revision, Clinical Modification codes. The outcomes included overall mortality, length of hospitalization, and healthcare expenditure related to hospitalization.
RESULTS: Out of all patients, 53,765 (3.97%) had concurrent CDI and liver cirrhosis. Diabetes mellitus, alcohol abuse, and acquired immunodeficiency were observed more in patients with liver cirrhosis. Overall mortality (adjusted odds ratio (aOR) 1.65, 95% confidence interval (CI) 1.53 - 1.77, P < 0.001), cost of hospitalization and length of hospital stay (11.0 vs. 10.4 days, P < 0.001) were significantly higher in patients with cirrhosis.
CONCLUSIONS: Patients with CDI and liver cirrhosis have significantly higher mortality, prolonged hospitalization and healthcare expenditure. Further studies are recommended to look at reversible risk factors for CDI in patients with liver cirrhosis to guide quality measures that would ultimately improve outcomes. Copyright 2020, Abdalla et al.

Entities:  

Keywords:  Cirrhosis; Clostridioides difficile; Hospital outcomes; Mortality

Year:  2020        PMID: 32362963      PMCID: PMC7188361          DOI: 10.14740/gr1240

Source DB:  PubMed          Journal:  Gastroenterology Res        ISSN: 1918-2805


Introduction

Clostridioides difficile is a gram-positive bacterium that was initially thought to be benign and isolated from the fecal flora of healthy newborns [1]. Bartlet [2] described its association with pseudomembranous colitis, and by the late 1980s, his team described multiple aspects of this illness. In the USA, Clostridioides difficile infection (CDI) is a common healthcare-associated infection (HCAI). The incidence of CDI has increased dramatically over the past two decades [3]. Multiple CDI outbreaks in acute care facilities have been attributed to the North American pulsed-field gel electrophoresis type 1 (NAP1) strain [4, 5]. Broad-spectrum antibiotics, prolonged hospitalization, advanced age, renal insufficiency, multiple comorbidities, immunosuppression, use of proton pump inhibitors (PPIs), and hypoalbuminemia are some of the widely recognized risk factors for CDI [4, 6-8]. Patients with liver cirrhosis have poor immunity, weaker immune response during illness, and a propensity for increased bacterial translocation and endotoxemia [9]. CDI is an independent mortality risk factor in patients with chronic liver disease similar to hepatic encephalopathy, spontaneous bacterial peritonitis and variceal bleeding [10]. Patients with liver cirrhosis and concurrent CDI have worse outcomes when compared to those without CDI. We conducted this study to assess the outcomes of CDI in patients with and without liver cirrhosis between 2012 and 2015.

Materials and Methods

Data source

The National Inpatient Sample (NIS) database is one of the largest inpatient databases that includes more than 4,000 hospitals and an estimated average of eight million admissions annually. It provides a large number of clinical and nonclinical variables from many hospitals that can be utilized to estimate outcomes for various clinical conditions and patient populations [11].

Study design

We used the International Classification of Disease, Ninth Revision, Clinical Modification (ICD-9-CM) to select our study population. Patients admitted with CDI as a primary or secondary diagnosis were identified using ICD-9-CM code 008.45. Only patients who were admitted between January 2012 and September 2015 were included in the study as the administrative data for hospitals started implementing ICD-10-CM in October 2015. Patients with a history of liver cirrhosis were identified using the ICD-9-CM codes 571.2, 571.6 and 571.5 (Fig. 1). We looked at the in-hospital mortality, length of stay (LOS), and hospitalization as the final outcomes. We also collected demographic information in addition to other comorbid conditions and risk factors.
Figure 1

Population derivation.

Population derivation.

Statistical analysis

NIS database was analyzed using SAS 9.4 (SAS Institute Inc., Cary, NC, USA). Continuous variables were described in the form of means ± standard deviations (SDs). Chi-square test and Student’s t-test were utilized to analyze categorical and continuous variables, respectively. Adjusted in-hospital mortality was calculated by multivariate logistic regression analysis. Patient variables, hospital characteristics, and comorbid conditions were analyzed using multivariate models. Statistical significance was set at a two-sided value of P < 0.05.

Results

A total of 1,327,595 patients with CDI were hospitalized between January 2012 and September 2015. Of them, 3.97% (52,765) had a history of concurrent liver cirrhosis. The mean age for patients with liver cirrhosis was 60 years compared to 67 years for those without a history of liver cirrhosis. Most of our patients were Caucasians (71%) and women (58%). Diabetes mellitus, alcohol abuse, acquired immunodeficiency, and solid tumors were noted significantly more in patients with liver cirrhosis. Patients with cirrhosis were more likely to be admitted to large urban teaching hospitals (66.1% vs. 58.2%, P < 0.001) and to have private insurance (19.5% vs. 17.6%, P < 0.001). The inpatient mortality was higher in patients with CDI and cirrhosis (10.1% vs. 6.9%, P < 0.001). The LOS (11 days vs. 10.4 days) and cost (23,055 vs. 26,535) were also significantly different between the two groups after adjusted analysis (Tables 1, 2).
Table 1

Baseline Characteristics of Index Hospitalizations Secondary to CDI

VariablesNo cirrhosisCirrhosisTotalP value
Patient level variables
  Mean age67.4 ± 17.260.3 ± 12.8< 0.001
  Gender< 0.0001
    Men521,505 (41.0%)28,900 (54.8%)550,405 (41.5%)
    Women753,245 (59.0%)23,865 (45.2%)777,110 (58.5%)
  Race< 0.0001
    White909,590 (71.4%)35,085 (66.5%)944,675 (71.2%)
    Black157,500 (12.3%)5,785 (11.0%)163,285 (12.3%)
    Others207,725 (16.3%)11,890 (22.5%)219,615 (16.5%)
  Comorbidities
    Obesity145,400 (11.4%)6,005 (11.4%)151,405 (11.4%)0.8606
    Congestive heart failure255,360 (20.0%)8,835 (16.7%)264,195 (20.0%)< 0.0001
    History of hypertension787,230 (61.8%)27,350 (51.8%)814,580 (61.4%)< 0.0001
    Diabetes280,525 (22.0%)13,485 (25.6%)294,010 (22.2%)< 0.0001
    Alcohol abuse48,320 (3.8%)19,950 (37.8%)68,270 (5.1%)< 0.0001
    Toxic megacolon1,925 (0.2%)50 (0.1%)1,975 (0.2%)0.001
    Acquired immune deficiency syndrome5,635 (0.4%)535 (1.0%)6,170 (0.5%)< 0.0001
    Metastatic cancer53,275 (4.2%)1,165 (2.2%)54,440 (4.1%)< 0.0001
    Solid tumor without metastasis49,580 (3.9%)2,520 (4.8%)52,100 (4.0%)< 0.0001
    Renal failure332,890 (26.1%)13,930 (26.4%)346,820 (26.1%)0.1406
    Chronic lung disease313,575 (24.6%)12,305 (23.3%)325,880 (24.6%)< 0.0001
  Primary payer< 0.0001
    Medicare/medicaid992,350 (77.9%)38,180 (72.4%)1,030,530 (77.6%)
    Private insurance224,575 (17.6%)10,300 (19.5%)234,875 (17.7%)
    Self-pay/others57,615 (4.5%)4,265 (8.1%)61,880 (4.7%)
Hospital characteristics
  Hospital bed size< 0.0001
    Small193,270 (15.2%)6,770 (12.8%)200,040 (15.1%)
    Medium344,310 (27.0%)14,080 (26.7%)358,390 (27.0%)
    Large737,250 (57.8%)31,915 (60.5%)769,165 (57.9%)
  Hospital location/teaching status< 0.0001
    Rural115,830 (9.1%)2,995 (5.7%)118,825 (9.0%)
    Urban nonteaching416,975 (32.7%)14,905 (28.3%)431,880 (32.5%)
    Urban teaching742,025 (58.2%)34,865 (66.1%)776,890 (58.5%)
  Disposition< 0.0001
    Home465,470 (36.5%)20,885 (39.6%)486,355 (36.7%)
    Facility/others713,590 (56.0%)25,855 (49.0%)739,445 (55.7%)
    AMA7,040 (0.6%)685 (1.3%)7,725 (0.6%)
    Died88,190 (6.9%)5,315 (10.1%)93,505 (7.0%)
  Cost< 0.001
    Mean23,055.6 ± 39,926.926,535.3 ± 41,379.2
  Length of stay< 0.001
    Mean10.4 ± 13.211.0 ± 12.9

AMA: against medical advice; CDI: Clostridioides difficile infection.

Table 2

Adjusted Mortality of CDI Admissions

Outcomes (mortality)Adjusted odds ratioLower limitUpper limitP value
Without cirrhosisReferenceReferenceReferenceReference
With cirrhosis1.651.531.77< 0.001

Adjusted with age, gender, hospital level characteristics (hospital type, bed-size) and comorbidities (obesity, congestive heart failure, hypertension, diabetes mellitus, metastatic cancer, immunodeficiency, alcohol abuse, toxic megacolon, renal failure, chronic lung disease). CDI: Clostridioides difficile infection.

AMA: against medical advice; CDI: Clostridioides difficile infection. Adjusted with age, gender, hospital level characteristics (hospital type, bed-size) and comorbidities (obesity, congestive heart failure, hypertension, diabetes mellitus, metastatic cancer, immunodeficiency, alcohol abuse, toxic megacolon, renal failure, chronic lung disease). CDI: Clostridioides difficile infection.

Discussion

Almost 4% of all admitted patients with CDI had a history of liver cirrhosis. This is lower than the prevalence of liver cirrhosis in the general population (4.5% to 9.0%) [12]. The in-hospital mortality in patients was significantly higher in patients with CDI and liver cirrhosis when compared to the cohort without cirrhosis (odds ratio (OR) 1.65, 95% confidence interval (CI) 1.53 - 1.77, P < 0.001) after adjusting for patient-level variables, comorbidities and hospital-level characteristics. We adjusted for alcohol abuse, immunodeficiency, toxic megacolon, metastatic cancer, congestive heart failure and chronic renal disease. Bajaj et al [10] demonstrated that mortality in patients with liver cirrhosis and CDI (13.8%) was significantly higher than in patients with cirrhosis (8.2%) or CDI (9.6%) alone. Rosenblatt et al [13] found CDI to be an independent risk factor for mortality in the same patient population. This could possibly be related to generalized suppression of defense mechanism associated with liver failure, effects of hypoalbuminemia and increased risk of bacterial translocation resulting in spontaneous bacterial peritonitis in patients with chronic liver disease. Smith et al [14] reported prolonged LOS in patients with liver cirrhosis and CDI when compared to patients without CDI (15.1 days vs. 6.55 days). Bajaj et al [10] noted that LOS was as twice as long in patients with cirrhosis and CDI, compared to patients without CDI (14.4 days vs. 6.7 days). The length of hospital stay was prolonged for patients with CDI and liver cirrhosis as compared to those without cirrhosis but only by a minimal margin (11 days vs. 10.4 days). Although the difference was statistically significant, the effect of cirrhosis on the LOS for patients with CDI does not seem that remarkable as the effect of CDI on patients with cirrhosis. The reasons for the discrepancy in the observed results remain unclear and limited by the nature of the NIS database. The cost associated with in-hospital stay was significantly higher in patients with cirrhosis than in those without among the entire cohort with CDI. Dotson et al [15] conducted a similar study on the same database from 2009 and found similar findings. This could be related to complications secondary to chronic liver disease that resulted in further diagnostic and therapeutic endoscopies, admission to the intensive care unit (ICU) and additional treatments. It is hard to tell how much of the cost could be attributed directly to the LOS since the difference between the two groups was not that remarkable when it came to LOS. Overall, the outcomes of CDI in patients with liver cirrhosis were worse when compared to patients without liver cirrhosis. The impact of liver cirrhosis on LOS in patients with CDI is not as notable as that of CDI in patients with liver cirrhosis.

Limitations

The study is limited by utilizing the discharge diagnoses and the billing codes of the NIS database that subject the data to inaccuracy related to under documentation and missing codes. There were significant differences in patient-level variables, hospital characteristics and comorbidities between the two groups at baseline. We aimed to limit the effect of difference at baseline by running a multivariate analysis, but this would not account for all possible confounding factors between the two groups. We could not assess the CDI severity, stage of liver cirrhosis, use of prophylactic antibiotic therapy, invasive and surgical interventions of our study sample.

Conclusions

To our knowledge, this is the largest study to date looking at the outcomes of CDI in patients with liver cirrhosis. Patients with CDI and liver cirrhosis have significantly higher mortality, prolonged hospitalization and healthcare expenditure. Further studies are recommended to look at reversible risk factors for CDI in patients with liver cirrhosis to guide quality measures that would ultimately improve outcomes.
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1.  Risk of Clostridium difficile infection with acid suppressing drugs and antibiotics: meta-analysis.

Authors:  Chun Shing Kwok; Aaron Kobina Arthur; Chukwudubem Ifeanyichukwu Anibueze; Sonal Singh; Rodrigo Cavallazzi; Yoon Kong Loke
Journal:  Am J Gastroenterol       Date:  2012-04-24       Impact factor: 10.864

2.  An epidemic, toxin gene-variant strain of Clostridium difficile.

Authors:  L Clifford McDonald; George E Killgore; Angela Thompson; Robert C Owens; Sophia V Kazakova; Susan P Sambol; Stuart Johnson; Dale N Gerding
Journal:  N Engl J Med       Date:  2005-12-01       Impact factor: 91.245

Review 3.  The growing incidence and severity of Clostridium difficile infection in inpatient and outpatient settings.

Authors:  Sahil Khanna; Darrell S Pardi
Journal:  Expert Rev Gastroenterol Hepatol       Date:  2010-08       Impact factor: 3.869

4.  John G. Bartlett: Contributions to the discovery of Clostridium difficile antibiotic-associated diarrhea.

Authors:  Sherwood L Gorbach
Journal:  Clin Infect Dis       Date:  2014-09-15       Impact factor: 9.079

5.  Host and pathogen factors for Clostridium difficile infection and colonization.

Authors:  Vivian G Loo; Anne-Marie Bourgault; Louise Poirier; François Lamothe; Sophie Michaud; Nathalie Turgeon; Baldwin Toye; Axelle Beaudoin; Eric H Frost; Rodica Gilca; Paul Brassard; Nandini Dendukuri; Claire Béliveau; Matthew Oughton; Ivan Brukner; Andre Dascal
Journal:  N Engl J Med       Date:  2011-11-03       Impact factor: 91.245

6.  Community-associated Clostridium difficile infection among older people in Tayside, Scotland, is associated with antibiotic exposure and care home residence: cohort study with nested case-control.

Authors:  Charis A Marwick; Ning Yu; Michael C Lockhart; Christopher C McGuigan; Camilla Wiuff; Peter G Davey; Peter T Donnan
Journal:  J Antimicrob Chemother       Date:  2013-07-03       Impact factor: 5.790

7.  The Epidemiology of Cirrhosis in the United States: A Population-based Study.

Authors:  Steven Scaglione; Stephanie Kliethermes; Guichan Cao; David Shoham; Ramon Durazo; Amy Luke; Michael L Volk
Journal:  J Clin Gastroenterol       Date:  2015-09       Impact factor: 3.062

8.  Predictors of Mortality in Cirrhosis Inpatients With Clostridium difficile Infection.

Authors:  Elliot Z Smith; Patrick G Northup; Curtis K Argo
Journal:  J Clin Gastroenterol       Date:  2018-09       Impact factor: 3.062

9.  Clostridium difficile is associated with poor outcomes in patients with cirrhosis: A national and tertiary center perspective.

Authors:  Jasmohan S Bajaj; Ashwin N Ananthakrishnan; Muhammad Hafeezullah; Yelena Zadvornova; Alexis Dye; Emily L McGinley; Kia Saeian; Douglas Heuman; Arun J Sanyal; Raymond G Hoffmann
Journal:  Am J Gastroenterol       Date:  2009-10-20       Impact factor: 10.864

Review 10.  Immune dysfunction in cirrhosis.

Authors:  Nora Sipeki; Peter Antal-Szalmas; Peter L Lakatos; Maria Papp
Journal:  World J Gastroenterol       Date:  2014-03-14       Impact factor: 5.742

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Review 1.  Clostridioides difficile Infection in Liver Cirrhosis: A Concise Review.

Authors:  Yuanbin Liu; Mingkai Chen
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