"Never doubt that a small group of thoughtful, committed citizens can change the world. Indeed, it is the only thing that ever has."

Margaret Mead

Original article

The Impact of Clostridium Difficile Infections on In-Hospital Outcomes of Venous Thromboembolism (Deep Vein Thrombosis or Pulmonary Embolism) Hospitalizations



Clostridium difficile infection (CDI) is associated with high mortality. Studies have shown an increased rate of venous thromboembolism (VTE) in patients with CDI. However, literature regarding the impact of CDI on outcomes of VTE-related hospitalizations is scarce. Our study aimed to assess the impact of CDI on in-hospital outcomes among VTE hospitalizations.


The 2016 National Inpatient Sample (NIS) was used to identify all adult hospitalizations in the United States with a primary discharge diagnosis of acute VTE. Hospitalizations with deep vein thrombosis (DVT) or pulmonary embolism (PE) were included under VTE. The sample was stratified based on the presence or absence of active CDI. Chi-square test and weighted Student’s t-test were used to analyze categorical and continuous variables, respectively. The adjusted odds ratio (OR) for clinical outcomes were calculated using multivariate logistic regression analysis. Subgroup analyses for DVT and PE hospitalizations were performed. All analyses were completed in SAS (SAS Institute Inc., Cary, NC), and a p-value of <0.05 was considered statistically significant.


We identified 382,585 weighted hospitalizations for VTE. Among them, 0.8% had concomitant CDI. The presence of CDI was associated with a statistically significant increase in in-hospital mortality (6% vs. 3%), hospitalization cost ($147,356.5 vs. $55,193), and length of stay (13.7 vs. 5.4 days). There were more incidents of bleeding and acute respiratory failure requiring prolonged ventilation in patients with CDI. The odds of stroke were significantly higher in patients with CDI and DVT.


CDI independently increased in-hospital mortality in VTE. Preventing CDI in the VTE population may mitigate complications, improve in-hospital outcomes, and reduce treatment costs.


Clostridium difficile infection (CDI) is a leading cause of nosocomial infection, resulting in a significant healthcare burden, morbidity, and mortality [1]. According to the literature, there was a two-fold increase in the incidence of CDI among hospitalized adults in the United States between 2001 and 2010, with more recent data suggesting approximately 365,000 CDI cases reported in the United States annually [2].

It is well-known that the pathogenesis of venous thromboembolism (VTE) involves the Virchow’s triad: stasis, endothelial injury, and hypercoagulability. Various studies have shown an increased rate of VTE in patients with CDI, likely secondary to the formation of a proinflammatory state [3,4]. However, data is scarce regarding the impact of CDI on outcomes of VTE hospitalizations. It is possible that CDI leads to poorer outcomes in these patients, whether due to a direct effect of CDI (prolonged hospital stay and associated complications), or due to the proposed effect of CDI on coagulability, which might be seen in terms of sequelae of clot extension, anticoagulation failure, embolic events, or bleeding complications. In this study, we sought to assess the impact of the presence or absence of CDI on outcomes of VTE hospitalizations.

Materials & Methods

Data were extracted from the 2016 Healthcare Cost and Utilization Project’s (HCUP) National Inpatient Sample (NIS). The NIS is the largest publicly available database in the United States and approximates a 20% stratified sample of discharges from US hospitals. In our analysis, all patients of ≥18 years of age who were identified with VTE-related hospitalizations [pulmonary embolism (PE) or deep vein thrombosis (DVT)] were included. Furthermore, VTE hospitalizations with and without CDI were identified, and their clinically relevant outcomes were compared. Given the publicly available nature of the dataset, the study was exempted from institutional review board (IRB) approval.

All statistical analyses followed the sample design elements (clusters, strata, and weights) provided by the NIS [5]. Continuous variables were reported as weighted means ±standard error (SE), and categorical variables were reported as weighted numbers and percentages. The standard errors of weighted means were estimated by using the Taylor linearization method that incorporates the sample design. Length of stay and total cost of hospitalization were normalized by log-transformation for all analyses, and antilog-transformed results from the multivariate linear regression models were then reported. The total costs of hospitalization were inflation-adjusted for 2018 using Consumer Price Index data provided by the US Department of Labor.

The differences in outcomes variables between hospitalizations with and without CDI were compared using weighted Student’s t-tests for continuous variables, and Rao-Scott modified chi-square tests for categorical variables. A multivariate logistic regression model was used to estimate the odds ratio (OR) of clinical outcomes after adjusting for patient demographics, hospital bed size, hospital location/teaching status, insurance type, household income, and relevant comorbidities, and incorporating hospital as a random effect. Subgroup analyses were conducted separately for hospitalizations with PE and DVT, again comparing in-hospital outcomes for those with and without CDI. Unadjusted and adjusted ORs and their corresponding 95% confidence intervals (CI) were reported. All statistical analyses were performed using the SAS Survey Procedures (SAS 9.4; SAS Institute Inc., Cary, NC). Statistical significance was defined by two-sided p-values of <0.05.


We identified 382,585 admissions with VTE. Of those, 3,080 (0.8%) had a concomitant diagnosis of CDI. The VTE population with CDI had a higher mean age compared to the VTE population without CDI (66.2 vs. 63.1 years, respectively). No statistically significant difference was found in terms of gender, race, or mean household income between both populations (Table 1).

Characteristics VTE hospitalizations with Clostridium difficile infections VTE hospitalizations without Clostridium difficile infections P-value
N (unweighted) 616 76,517
N (weighted) 3,080 382,585
  Mean SE Mean SE  
Age, years 66.2 0.6 63.1 0.1 < .0001
Length of stay, days 13.7 0.6 5.4 0.03 < .0001
Total cost of hospitalization, $ 147,357 12,734 55,193 764 < .0001
  Weighted N % Weighted N %  
Male 1,405 45.60% 182,305 47.70% 0.32
Female 1,675 54.40% 200,280 52.30%  
White 2,250 73.10% 271,240 70.90% 0.2
Black 440 14.30% 69,680 18.20%  
Hispanic 235 7.60% 26,865 7%  
Asian or Pacific Islander 45 1.50% 4,075 1.10%  
Native American 15 0.50% 1,490 0.40%  
Other 95 3.10% 9,235 2.40%  
Insurance type          
Medicare 2,010 65.30% 202,675 53% < .0001
Medicaid 365 11.90% 48,995 12.80%  
Private 570 18.50% 103,955 27.20%  
Self-pay 65 2.10% 14,240 3.70%  
Other 65 2.10% 11,170 2.90%  
Hospital region          
Northeast 645 20.90% 76,725 20.10% 0.001
Midwest 615 20% 85,945 22.50%  
South 1,135 36.90% 157,225 41.10%  
West 685 22.20% 62,690 16.40%  
Hospital location/teaching status          
Rural 125 4.10% 33,505 8.80% < .0001
Urban non-teaching 850 27.60% 104,790 27.40%  
Urban teaching 2,105 68.30% 244,290 63.90%  
Hospital bed size          
Small 440 14.30% 71,310 18.60% 0.026
Medium 920 29.90% 110,225 28.80%  
Large 1,720 55.80% 201,050 52.60%  
Household income          
Q1 800 26% 116,220 30.40% 0.075
Q2 895 29.10% 97,850 25.60%  
Q3 750 24.40% 91,365 23.90%  
Q4 635 20.60% 77,150 20.20%  
In-hospital mortality 185 6% 11,385 3% 0.002
Renal failure 635 20.60% 50,745 13.30% < .0001
Deficiency anemia 1,105 35.90% 82,910 21.70% < .0001
Congestive heart failure 665 21.60% 47,070 12.30% < .0001
Metastatic cancer 410 13.30% 28,715 7.50% < .0001
Sepsis 250 8.10% 5,070 1.30% < .0001
Paralysis 220 7.10% 12,380 3.20% 0.0002
Diabetes, complicated 415 13.50% 37,255 9.70% 0.005
Liver disease 185 6% 13,865 3.60% 0.021
Coagulopathy 370 12% 29,710 7.80% 0.001
Prior VTE 330 10.70% 51,570 13.50% 0.03
Hyperlipidemia 755 24.50% 112,925 29.50% 0.004
Obesity 400 13% 81,050 21.20% < .0001
Smoking 325 10.60% 54,250 14.20% 0.004
Hypertension 1,820 59.10% 231,665 60.60% 0.47
Solid tumor without metastasis 240 7.80% 21,725 5.70% 0.058
Lymphoma 75 2.40% 4,960 1.30% 0.069
Rheumatoid arthritis/collagen vascular disease 140 4.50% 14,835 3.90% 0.422
Peripheral vascular disease 205 6.70% 19,965 5.20% 0.163
Chronic pulmonary disease 675 21.90% 89,545 23.40% 0.369
Diabetes, uncomplicated 390 12.70% 56,045 14.60% 0.131
Alcohol abuse 150 4.90% 13,820 3.60% 0.144

The VTE population with concomitant CDI was found to have higher prevalence of comorbidities compared to those without CDI, including renal failure (20.6% vs. 13.3%), congestive heart failure (35.9% vs. 21.7%), complicated diabetes (13.5% vs. 9.7%), metastatic cancer (13.3% vs. 7.5%), liver disease (6% vs. 3.6%), deficiency anemia (35.9% vs. 21.7%), coagulopathy (12% vs. 7.8%) and paralysis (7.1% vs. 3.2%). They were also more likely to present with sepsis (8.1% vs. 1.3%). However, the VTE population without CDI had a higher prevalence of hyperlipidemia (29.5% vs. 24.5%), obesity (21.2% vs. 13%), smoking (14.2% vs. 10.6%), and prior VTE (13.5% vs. 10.7%). VTE hospitalizations with CDI were found to have increased in-hospital mortality (6% vs. 3%, adjusted OR: 1.54, 95% CI: 1.09-2.17, p = 0.014), longer mean length of hospital stay (13.7 days vs. 5.4 days, adjusted OR: 2.10, 95% CI: 1.98-2.24, p: <0.001) and hospitalization cost ($147,356.5 vs. $55,193, adjusted OR: 2.01, 95% CI: 1.87-2.17, p: <0.001) (Table 2).

Variables VTE patients
  No Clostridium difficile infections Clostridium difficile infections P-value
In-hospital mortality      
Incidence, % 3 6  
Adjusted OR (95% CI)* Ref 1.54 (1.09–2.17) 0.014
Incidence, % 9.9 24.2  
Adjusted OR (95% CI)* Ref 2.32 (1.9–2.84) < .0001
Incidence, % 0.3 0.6  
Adjusted OR (95% CI)* Ref 1.6 (0.58–4.42) 0.37
Shock state      
Incidence, % 1.9 7.8  
Adjusted OR (95% CI)* Ref 3.21 (2.35–4.39) < .0001
Incidence, % 6.4 16.9  
Adjusted OR (95% CI)* Ref 2.55 (2.05–3.17) < .0001
Incidence, % 0.1 0.2  
Adjusted OR (95% CI)* Ref 0.8 (0.11–6.01) 0.83
Acute respiratory failure      
Incidence, % 7.4 18  
Adjusted OR (95% CI)* Ref 2.22 (1.8–2.76) < .0001
Incidence, % 0.4 0.5  
Adjusted OR (95% CI)* Ref 0.76 (0.24–2.39) 0.64
Mechanical ventilation for >96 hours      
Incidence, % 1.2 6  
Adjusted OR (95% CI)* Ref 4.33 (3.05–6.16) < .0001
Length of stay      
Mean ±SE 5.4 ±0.03 13.7 ±0.6  
Adjusted parameter estimate (95% CI)*† Ref 2.10 (1.98–2.24) < .0001
Average hospital costs      
Mean ±SE 55,193 ±764 147,356.5 ±12,734.1  
Adjusted parameter estimate (95% CI)*† Ref 2.01 (1.87–2.17) < .0001

Notably, CDI in VTE hospitalizations was independently associated with increased risk of bleeding, acute kidney injury (AKI), shock state, acute respiratory failure requiring mechanical ventilation for >96 hours (p: <0.001 for all; adjusted for age, race, sex, insurance status, hospital characteristics, and all significant comorbidities listed in Table 1) (Figure 1).

Subgroup analyses of DVT vs. PE hospitalizations were also performed. For both groups, hospitalizations with concomitant CDI had an increased risk of AKI, bleeding, and acute respiratory failure needing mechanical ventilation for >96 hours (p: <0.001 for all, adjusted for age, race, sex, insurance status, hospital characteristics, and all significant comorbidities listed in Table 1) (Table 3).

Variables PE hospitalizations DVT hospitalizations
  No Clostridium difficile infections Clostridium difficile infections P-value No Clostridium difficile infections Clostridium difficile infections P-value
In-hospital mortality            
Incidence, % 4.5 7.9   0.8 1.9  
Adjusted OR (95% CI)* Ref 1.39 (0.97–2.0) 0.072 Ref 1.85 (0.57–5.96) 0.31
Incidence, % 11.7 24.7   7 23.7  
Adjusted OR (95% CI)* Ref 2.07 (1.63–2.62) < .0001 Ref 2.97 (1.97–4.48) < .0001
Incidence, % 0.4 0.2   0.2 1.9  
Adjusted OR (95% CI)* Ref 0.48 (0.07–3.5) 0.47 Ref 6.38 (1.83–22.15) 0.0036
Shock state            
Incidence, % 3 10.6   0.3 1.3  
Adjusted OR (95% CI)* Ref 2.97 (2.15–4.11) < .0001 Ref 2.51 (0.59–10.62) 0.2122
Incidence, % 7.4 18.7   5.3 14.1  
Adjusted OR (95% CI)* Ref 2.47 (1.92–3.17) < .0001 Ref 2.69 (1.7–4.27) < .0001
Incidence, % 0.2 0.2   0.0004 0  
Adjusted OR (95% CI)* Ref 0.91 (0.12–6.95) 0.93 Ref NA NA
Acute respiratory failure            
Incidence, % 11.2 23.3   1.3 5.1  
Adjusted OR (95% CI)* Ref 1.99 (1.58–2.51) < .0001 Ref 2.73 (1.24–5.99) 0.0125
Incidence, % 0.6 0.2   0.1 1.3  
Adjusted OR (95% CI)* Ref 0.24 (0.03–1.75) 0.16 Ref 6.21 (1.34–28.73) 0.0195
Mechanical ventilation for >96 hours            
Incidence, % 1.8 8.1   0.2 1.3  
Adjusted OR (95% CI)* Ref 3.93 (2.72–5.67) < .0001 Ref 4.5 (1.02–19.8) 0.0464
Length of stay            
Mean ±SE 5.9 ±0.05 14.5 ±0.8   5.0 ±0.04 12.5 ±1.2  
Adjusted parameter estimate (95% CI)*† Ref 2.05 (1.88–2.23) < .0001 Ref 1.99 (1.76–2.24) < .0001
Average hospital costs            
Mean ±SE 60,903.1 ±985.7 166,302.7 ±17,358.8 < .0001 47,306.4 ±655 108,513.9 ±12,478 < .0001
Adjusted parameter estimate (95% CI)*† Ref 2.16 (2.00–2.33)   Ref 1.84 (1.59–2.14)  

The odds of shock were greater in CDI and PE group (10.6% vs. 3%, adjusted OR: 2.97, 95% CI: 2.15-4.11, p: <0.001) (Figure 2), whereas the odds of stroke were higher in hospitalizations with CDI and DVT (1.3% vs. 0.1%, adjusted OR: 6.21, 95% CI: 1.5-25.71, p: <0.01) (Table 3) (Figure 3).


CDIs pose a significant burden on healthcare systems, not just in the United States but across the world [6]. Past studies have demonstrated a two-fold increase in the incidence of CDI among hospitalized adults in the United States between 2001-2010 [2]. Data from 2012 showed that annual cost for management of CDI amounted to approximately $800 million in the United States and €3,000 million in Europe, barring the costs for secondary complications [7]. While the rate of healthcare-associated CDI decreased in the United States between 2011-2017 by an estimated 36%, the rate of community-associated CDI has not changed in that time and now accounts for nearly half of all infections [8]. CDI has also been shown to have an independent association with the development of VTE, and findings of associations between acute infections and increased risk of VTE support the hypothesis that CDI may be causing a proinflammatory, procoagulant state in the human body [9-11].

While the association between CDI and increased risk of VTE is known, data regarding the impact of CDI on outcomes of these cases remain scarce. Our study, to the best of our knowledge, is the first of its kind to assess the outcomes of VTE in the presence of CDI, and the data we present here suggest that the presence of CDI independently causes a substantial increase in healthcare costs. This can be seen directly in terms of increased raw cost of VTE hospitalizations, and also in terms of increased mean length of stay, AKI, bleeding complications, shock, and the need for mechanical ventilation.

Fully understanding the burden CDI places on healthcare is critical to ensure adequate allocation of resources to CDI treatment and prevention efforts. Also, understanding its impact in the setting of DVT and PE admissions, themselves sources of considerable morbidity and healthcare cost, would seem essential. This is of particular importance when considering the apparent success of infection control programs and reduced prescriptions of fluoroquinolones in reducing the rates of healthcare-associated CDI, suggesting that there are interventions whose widespread adoption could further reduce rates of CDI and its associated complications [12].

Many of the clinical outcomes presented here can be attributed to CDI, causing a systemic proinflammatory state, with hypovolemia secondary to gastrointestinal losses, and third spacing secondary to inflammation. This drives outcomes like shock, AKI, and the need for dialysis. CDI patients with VTE outcomes seem to have more underlying comorbidities in general, and these, in turn, may put them at a higher risk of prolonged hospital stay and poor clinical outcomes. However, the adverse outcomes mentioned here were found after adjusting for these comorbidities, suggesting that CDI is an independent cause of serious adverse events in VTE hospitalizations.

Both the DVT and PE subgroups showed an increased risk of the need for prolonged mechanical ventilation (>96 hours) for CDI hospitalizations, which is somewhat surprising. In PE patients, it might reflect a combination of both ventilation/perfusion (V/Q) mismatch from PE and systemic inflammatory state from CDI. However, the presence of the effect in DVT hospitalizations, with a comparable OR (3.93 in PE patients, 4.5 in DVT patients), suggests that the presence of thrombotic events marks greater disease severity in CDI. Though speculative, it prompts a need for further investigation, both in terms of research, and a higher index of suspicion for thrombotic events in CDI hospitalizations. The elevated risk of shock in hospitalizations with PE and CDI versus PE without CDI is less surprising and might be explained by the addition of obstructive elements to existing hypovolemic and distributive shock from CDI. Interestingly, the population with VTE but no CDI had a higher prevalence of hyperlipidemia, obesity, smoking, and prior VTE. All of these are independent risk factors for VTE, and their decreased prevalence in the VTE with CDI group further supports the theory that CDI is a separate cause of thrombotic disease burden. Further studies are warranted to determine the causality of these outcomes, which may impact how we approach treating patients with CDI while being cognizant of the possible complications caused by VTEs in this high-risk population. As for the marked increase in the incidence of stroke noted among CDI hospitalizations with DVT, which was absent among hospitalizations with CDI and PE, it is challenging to explain. While risk factors for arterial and venous thrombotic diseases are shared, the stroke itself being a notorious risk factor for the development of recurrent CDIs, and for VTE, the risks of developing PE and DVT after stroke are very similar [13]. This may be a fruitful area for further study.

Our study has a few limitations. Firstly, our analysis was retrospective in nature. Hence, it was difficult to ascertain the causal relationship between CDI and VTE. Secondly, given the observational nature of the study, we found it hard to identify and adjust for all possible confounders. Thirdly, as a database study, it was implausible to determine with certainty if a specific diagnosis had been made during the hospitalization of record or if a patient had carried a history of such a diagnosis. Lastly, one NIS entry is equivalent to one hospitalization. Hence, a single patient may account for multiple entries if hospitalized more than once within the study period. However, despite these limitations, we believe the results still highlight the significance of CDI infections in patients admitted for VTE.


Our study, to the best of our knowledge, is the first study of its kind to assess the outcomes of VTE in the presence of CDI. CDI remains a considerable burden in terms of increased length of hospital stay and healthcare costs, and it independently increases the risk of in-hospital mortality and various complications in VTE patients. Taking adequate steps to prevent CDI in the VTE population may avert unforeseen complications, improve in-hospital outcomes, and reduce healthcare costs.


  1. Kanamori H, Weber DJ, DiBiase LM, et al.: Longitudinal trends in all healthcare-associated infections through comprehensive hospital-wide surveillance and infection control measures over the past 12 years: substantial burden of healthcare-associated infections outside of intensive care units and “other” types of infection. Infect Control Hosp Epidemiol. 2015, 36:1139-1147. 10.1017/ice.2015.142
  2. Reveles KR, Lee GC, Boyd NK, Frei CR: The rise in Clostridium difficile infection incidence among hospitalized adults in the United States: 2001-2010. Am J Infect Control. 2014, 42:1028-1032. 10.1016/j.ajic.2014.06.011
  3. Barmparas G, Fierro N, Lamb AW, et al.: Clostridium difficile increases the risk for venous thromboembolism. Am J Surg. 2014, 208:703-709. 10.1016/j.amjsurg.2014.05.025
  4. Dai C, Cao Q, Sun MJ: Venous thromboembolism in hospitalized inflammatory bowel disease patients with Clostridium difficile infection. Inflamm Bowel Dis. 2018, 24:662. 10.1093/ibd/izx068
  5. Houchens R, Ross D, Elixhauser A, Jiang J: Nationwide Inpatient Sample (NIS) Redesign Final Report. US Agency for Healthcare Research and Quality, Rockville, MD; 2014.
  6. Reigadas Ramírez E, Bouza ES: Economic burden of Clostridium difficile infection in European countries. Adv Exp Med Biol. 2018, 1050:1‐12. 10.1007/978-3-319-72799-8_1
  7. Bouza E: Consequences of Clostridium difficile infection: understanding the healthcare burden. Clin Microbiol Infect. 2012, 18:5-12. 10.1111/1469-0691.12064
  8. DePestel DD, Aronoff DM: Epidemiology of Clostridium difficile infection. J Pharm Pract. 2013, 26:464-475. 10.1177/0897190013499521
  9. Schmidt M, Horvath-Puho E, Thomsen RW, Smeeth L, Sørensen HT: Acute infections and venous thromboembolism. J Intern Med. 2012, 271:608-618. 10.1111/j.1365-2796.2011.02473.x
  10. Smeeth L, Cook C, Thomas S, Hall AJ, Hubbard R, Vallance P: Risk of deep vein thrombosis and pulmonary embolism after acute infection in a community setting. Lancet. 2006, 367:1075-1079. 10.1016/S0140-6736(06)68474-2
  11. Clayton TC, Gaskin M, Meade TW: Recent respiratory infection and risk of venous thromboembolism: case-control study through a general practice database. Int J Epidemiol. 2011, 40:819-827. 10.1093/ije/dyr012
  12. Dubberke ER: Prevention of healthcare‐associated Clostridium difficile: what works?. Infect Control Hosp Epidemiol. 2010, 31:S38‐S41. 10.1086/655985
  13. Previtali E, Bucciarelli P, Passamonti SM, Martinelli I: Risk factors for venous and arterial thrombosis. Blood Transfus. 2011, 9:120-138. 10.2450/2010.0066-10


Deep vein thrombosis Pulmonary embolism Clostridium difficile infections Smoking Alcohol abuse Prior venous thromboembolism Hyperlipidemia Obesity Congestive heart failure Peripheral vascular disease Diabetes, uncomplicated DIC
I82401' I2692' A047' F17200' F1010' Z86718' E785' 'E6601' I099 I700' E100 D65'
I82402' I2602' A0471' F17201' F1011' I82701'   'E6609' I110 I701' E101   
I82403' I2609' A0472' F17203' F10120' I82702'   'E661' I130 I70201' E109   
I82409' I2699'   F17208' F10121' I82703'   'E662' I132 I70202' E110   
I82411'     F17209' F10129' I82709'   'E663' I255 I70203' E111   
I82412'     F17210' F1014' I82711'   'E668' I420  I70208' E119   
I82413'     F17211' F10150' I82712'   'E669' I425 I70209' E120   
I82419'     F17213' F10151' I82713'   'Z6825' I429 I70211' E121   
I82421'     F17218' F10159' I82719'   'Z6826' I43 I70212' E129   
I82422'     F17219' F10180' I82721'   'Z6827' P290 I70213' E130   
I82423'     F17220' F10181' I82722'   'Z6828' I501' I70218' E131   
I82429'     F17221' F10182' I82723'   'Z6829' I5020' I70219' E139   
I82431'     F17223' F10188' I82729'   'Z6830' I5021' I70221' E140   
I82432'     F17228' F1019' I82501'   'Z6831' I5022' I70222' E141   
I82433'     F17229'   I82502'   'Z6832' I5023' I70223' E149  
I82439'     F17290'   I82503'   'Z6833' I5030' I70228' E1100'  
I82441'     F17291'   I82509'   'Z6834' I5031' I70229' E1101'  
I82442'     F17293'   I82511'   'Z6835' I5032' I70231'  
I82443'     F17298'   I82512'   'Z6836' I5033' I70232'  
I82449'     F17299'   I82513'   'Z6837' I5040' I70233'  
I82491'         I82519'   'Z6838' I5041' I70234'  
I82492'         I82521'   'Z6839' I5042' I70235'  
I82493'         I82522'   'Z6841' I5043' I70238'  
I82499'         I82523'   'Z6842' I50810' I70239'  
I824Y1'         I82529'   'Z6843' I50811' I70241'  
I824Y2'         I82531'   'Z6844' I50812' I70242'  
I824Y3'         I82532'   'Z6845' I50813' I70243'  
I824Y9'         I82533'     I50814' I70244'  
I824Z1'         I82539'     I5082' I70245'  
I824Z2'         I82541'     I5083' I70248'  
I824Z3'         I82542'     I5084' I70249'  
I824Z9'         I82543'     I5089' I7025'  
I82A11'         I82549'     I509' I70291'  
I82601'         I82591'       I70292'  
I82602'         I82592'       I70293'  
I82603'         I82593'       I70298'  
I82609'         I82599'       I70299'  
I82611'         I825Y1'       I708'  
I82612'         I825Y2'       I7090'  
I82613'         I825Y3'       I7091'  
I82619'         I825Y9'       I7092'  
I82621'         I825Z1'       I7100'  
I82622'         I825Z2'       I7101'  
I82623'         I825Z3'       I7102'  
I82629'         I825Z9'       I7103'  
I82A12'         I82701'       I711'  
I82A13'         I82702'       I712'  
I82A19'         I82703'       I713'  
I82C11'         I82709'       I714'  
I82C12'         I82711'       I715'  
I82C13'         I82712'       I716'  
I82B11'         I82713'       I718'  
I82B12'         I82719'       I719'  
I82B13'         I82721'       I731  
I82B19'         I82722'       I738  
I82C19'         I82723'       I739  
          I82729'       I771  
          I82891'       I790  
          I82A21'       I792  
          I82A22'       K551  
          I82A23'       K558  
          I82A29'       K559  
          I82B21'       Z958  
          I82B22'       Z959  
Diabetes, complicated Hypertension Chronic kidney disease Acute kidney injury Surgery Sepsis Shock state Acute kidney injury + dialysis Bleeding Paralysis Acute respiratory failure Stroke  
E1021' 'I10' N181 N178 Y830' A4101' R570' N186' D62' G8100' J9601' I6300'  
E1022' 'I110' N182 N170 Y831' A4102' R571' Z992' I6000' G8101' J9602' I63011'  
E1029' 'I119' N183 N171 Y832' A411' R578' N178 I6001' G8102' J9600' I63012'  
E10311' 'I120' N184 N172 Y833' A412' R579' N170 I6002' G8103' J9620' I63013'  
E10319' 'I129' N186 N179 Y834' A413' R6521' N171 I6010' G8104' J9621' I63019'  
E10321' 'I130' N185   Y835' A414' T8110XA' N172 I6011' G8110' J9622' I6302'  
E103211' 'I1310' N189   Y836' A4150' T8110XD' N179 I6012' G8111' J9690' I63031'  
E103212' 'I1311' I1310'   Y838' A4151' T8110XS'   I602' G8112' J9691' I63032'  
E103213' 'I132'     Y839' A4152' T8111XA'   I6020' G8113' J9692' I63033'  
E103219' 'I150'       A4153' T8111XD'   I6021' G8114' R0603 I63039'  
E10329' 'I151'       A4159' T8111XS'   I6022' G8190' J80 I6309'  
E103291' 'I152'       A4181' T8112XA'   I6030' G8191' J810 I6310'  
E103292' 'I158'       A4189' T8112XD'   I6031' G8192' J95821 I63111'  
E103293' 'I159'       A419' T8112XS'   I6032' G8193' R092 I63112'  
E103299'         R6520' T8119XA'   I604' G8194' R0609 I63113'  
E10331'         T8119XD'   I6050' G8220' R0689 I63119'  
E103311'         T8119XS'   I6051' G8221'   I6312'  
E103312'           I6052' G8222'   I63131'  
E103313'           I606' G8250'   I63132'  
E103319'           I607' G8251'   I63133'  
E10339'           I608' G8252'   I63139'  
E103391'           I609' G8253'   I6319'  
E103392'           I610' G8254'   I6320'  
E103393'           I611' G830'   I63211'  
E103399'           I612' G8310'   I63212'  
E10341'           I613' G8311'   I63213'  
E103411'           I614' G8312'   I63219'  
E103412'           I615' G8313'   I6322'  
E103413'           I616' G8314'   I63231'  
E103419'           I618' G8320'   I63232'  
E10349'           I619' G8321'   I63233'  
E103491'           I6200' G8322'   I63239'  
E103492'           I6201' G8323'   I6329'  
E103493'           I6202' G8324'   I6330'  
E103499'           I6203' G8330'   I63311'  
E10351'           I621' G8331'   I63312'  
E103511'           I629' G8332'   I63313'  
E103512'           H35731' G8333'   I63319'  
E103513'           H35732' G8334'   I63321'  
E103519'           H35733' G834'   I63322'  
E103521'           H35739' G801'   I63323'  
E103522'           H3560' G802'   I63329'  
E103523'           H3561' G041'   I63331'  
E103529'           H3562' G800'   I63332'  
E103531'           H3563' G114'   I63333'  
E103532'           H31301'     I63339'
E103533'           H31302'     I63341'
E103539'           H31303'     I63342'
E103541'           H31309'     I63343'
E103542'           H31311'     I63349'
E103543'           H31312'     I6339'
E103549'           H31313'     I6340'
E103551'           H31319'     I63411'
E103552'           H31411'     I63412'
E103553'           H31412'     I63413'
E103559'           H31413'     I63419'
E10359'           H31419'     I63421'
E103591'           H47021'     I63422'
E103592'           H47022'     I63423'
E103593'           H47023'     I63429'
E103599'           H47029'     I63431'
E1036'           H4310'     I63432'
E1037X1'           H4311'     I63433'
E1037X2'           H4312'     I63439'
E1037X3'           H4313'     I63441'
E1037X9'           I621'     I63442'
E1039'           I312     I63443'
E1040'           S40011A'     I63449'
E1041'           S40011D'     I6349'
E1042'           S40011S'     I6350'
E1043'           S40012A'     I63511'
E1044'           S40012D'     I63512'
E1049'           S40012S'     I63513'
E1051'           S40019A'     I63519'
E1052'           S40019D'     I63521'
E1059'           S40019S'     I63522'
E10610'           S40021A'     I63523'
E10618'           S40021D'     I63529'
E10620'           S40021S'     I63531'
E10621'           S40022A'     I63532'
E10622'           S40022D'     I63533'
E10628'           S40022S'     I63539'
E10630'           S40029A'     I63541'
E10638'           S40029D'     I63542'
E10641'           S40029S'     I63543'
E10649'           M79A11'     I63549'
E1065'           M79A12'     I6359'
E1069'           M79A19'     I636'
E108'           M79A21'     I638'
E1121'           M79A22'     I6381'
E1122'           M79A29'     I6389'
E1129'           M79A3'     I639'
E11311'           M79A9'     I6601'
E11319'               I6602'
E11321'               I6603'
E113211'               I6609'
E113212'               I6611'
E113213'               I6612'
E113219'               I6613'
E11329'               I6619'
E113291'               I6621'
E113292'               I6622'
E113293'               I6623'
E113299'               I6629'
E11331'               I663'
E113311'               I668'
E113312'               I669'

Original article

The Impact of Clostridium Difficile Infections on In-Hospital Outcomes of Venous Thromboembolism (Deep Vein Thrombosis or Pulmonary Embolism) Hospitalizations

Author Information

Khushali Jhaveri Corresponding Author

Internal Medicine, The Georgetown University Hospital/MedStar Washington Hospital Center, Washington, DC, USA

Aniruddh Som

Internal Medicine, The Georgetown University Hospital/MedStar Washington Hospital Center, Washington, DC, USA

Sandeep A. Padala

Nephrology, Medical College of Georgia - Augusta University, Augusta, USA

Salim Surani

Internal Medicine, Corpus Christi Medical Center, Corpus Christi, USA

Internal Medicine, University of North Texas, Dallas, USA

Ethics Statement and Conflict of Interest Disclosures

Human subjects: Consent was obtained by all participants in this study. Animal subjects: All authors have confirmed that this study did not involve animal subjects or tissue. Conflicts of interest: In compliance with the ICMJE uniform disclosure form, all authors declare the following: Payment/services info: All authors have declared that no financial support was received from any organization for the submitted work. Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work. Other relationships: All authors have declared that there are no other relationships or activities that could appear to have influenced the submitted work.

Original article

The Impact of Clostridium Difficile Infections on In-Hospital Outcomes of Venous Thromboembolism (Deep Vein Thrombosis or Pulmonary Embolism) Hospitalizations

Figures etc.


Scholary Impact Quotient™ (SIQ™) is our unique post-publication peer review rating process. Learn more here.