2University of Central Florida College of Medicine/HCA Graduate Medical Education Consortium, Gainesville, Florida, 32605, USA
3Nassau University Medical Center, East Meadow, New York, 11554, USA
4Joan C. Edward School of Medicine at Marshall University, Huntington, West Virginia, 25755, USA
5Marshall University School of Pharmacy, Huntington, West Virginia, 25755, USA
Methods: In this cross-sectional study, hospitalization data were extracted from National Inpatient Sample (NIS) between 2005- 2014. International classification of disease, ninth revision, clinical modification codes (ICD 9 CM) were used to identify VTE and IBD. We have included all patients with primary or secondary diagnosis of VTE and IBD. Primary outcomes were in-hospitalization mortality and average length of stay. Our secondary outcomes were blood loss requiring transfusion, gastrointestinal hemorrhage and post-operative wound infection. Trend analysis was performed using Jonchheere-Terpstra Test.
Result: A total of 16,550 (weighted 82750) patients were included in our final analysis. Overall hospitalizations for IBD complicated by VTE are rising from 2005 to 2014. Overall, in-hospital mortality was 4.7% in IBD patients complicated by VTE. In-hospital mortality in IBD patients was 0.18% in 2005, which increased to 0.52% in 2014 (P for trend = < 0.0001). Average length of stay in IBD patients was 9.6 days in 2005 which increased to 10.9 days in 2014 (P for trend = < 0.0001).
Conclusion: Overall hospitalizations, in-hospital mortality and average length of stay for IBD complicated by VTE are rising since last decade; which is a serious health care concern. It is also suggestive of need to perform more detailed research in this area.
Key Words: Venous Thromboembolism; Inflammatory Bowel Disease; Trends; In-Hospital Outcomes
Abbreviations: IBD- Inflammatory Bowel Disease; VTE- Venous Thromboembolism; EIM- Extra Intestinal Manifestation; DVT- Deep Venous Thrombosis; PE- Pulmonary Embolism; NIS- National Inpatient Sample; US- Ulcerative Colitis; CD- Crohn’s Disease; CCI- Charlson’s Comorbidity Index
VTE prevention involves correcting modifiable risk factors, such as disease activity, vitamin deficiency, dehydration and prolonged immobilization. Recurrent VTE can be prevented by anticoagulant treatment, which can cause fatal bleeding. Thus, choosing the optimal duration of prophylaxis for an individual patient entails balancing the risk of bleeding against the risk of recurrent VTE [7-10].
We have included all patients with primary or secondary diagnosis of VTE and IBD. We have used International classification of disease, ninth revision; clinical modification codes (ICD 9 CM) to identify VTE (325, 451.11, 451.19, 451.2, 451.81, 451.83, 451.84, 452, 572.1, 453.0–453.3, 453.40–453.42, 453.8, 453.9, 415.1, 415.11, 415.12, and 415.19) and IBD (555 and 556). All patients below 18 years of age were excluded from our study. Patient’s selection chart is shown in figure 1. IBD groups have all the patients included in our study. “Both” category included those patients who had Ulcerative Colitis (UC) and Crohn’s Disease (CD) as their diagnosis. We used comorbidities given in the database which has been used previously [12]. For disease presentation, we have used appropriate ICD 9 CM procedural and diagnostic codes to identify active fistulizing disease or intra-abdominal abscess, active stricturing disease, bowel obstruction, perianal abscess, lower gastrointestinal bleeding, hypovolemia, and malnutrition [Supplementary Table 1] [13]. For in-hospital outcomes, we have used appropriate ICD 9 CM procedural and diagnostic codes to identify blood loss requiring transfusion, gastrointestinal hemorrhage, postoperative wound infection, and surgical complications [Supplementary Table 1] [13]. Appropriate ICD 9 CM codes were used to examine surgical complications [Supplementary Table 1] [13].
Variable Name |
ICD 9 CM Codes |
Venous Thromboembolism |
325, 451.11, 451.19, 451.2, 451.81, 451.83, 451.84, 452, 572.1, 453.0–453.3, 453.40–453.42, 453.8, 453.9, 415.1, 415.11, 415.12, and 415.19 |
Crohn’s Disease |
555 |
Ulcerative Colitis |
556 |
Active Fistulizing disease or intra-abdominal abscess |
537.4,567.2,569.5,593.3,596.1,619.1,567.21,567.22,569.81,569.83 |
Active Stricturing Disease |
560.9,537.3 |
Bowel Obstruction |
560,568 |
Perianal Abscess |
566 |
Unspecified Lower GI Bleeding |
578.9,569.3 |
Hypovolemia |
276.5 |
Malnutrition |
263 |
Endoscopic Procedure |
45.1,45.2,45.3,45.4,45.52,46.86 |
Incision, Excision and Anastomosis of Intestine |
45.0,45.9,45.5,45.6,45.33,45.50,45.51,45.61,45.62,45.63,45.90,45.91,45.93,45.94 |
Resection of Large Intestine |
45.7,45.8,45.81,45.82,45.83,45.92,45.93,45.94,45.95 |
Rectal and perirectal Surgery |
48 |
Other Surgery of small intestine |
46.0,46.4,46.5, 46.6,46.01,46.02,46.20,46.21,46.22,46.23,46.24,46.40,46.41, 46.50,46.51, 46.60,46.61,46.62,46.71,46.72,46.73,46.74,46.81,46.95 |
Other Surgery of large intestine |
46.1,46.03,46.04,46.10,46.11,46.13,46.14,46.42,46.43,46.52, 46.63,46.64, 46.75,46.76,46.79,46.82,46.87,46.91,46.92,46.96 |
Post-operative wound complication including infection, dehiscence, and fistula |
998.6,998.83,998.12,998.13,998.31,998.32 |
Variable Name |
IBD (N=16550) |
UC (N=7422) |
CD (N=9069) |
Both (N=59) |
|
Age (Years) |
57.4±17.9 |
59.7±18.3 |
55.6±17.3 |
53.2±17.3 |
|
Race* |
|||||
White |
80.5 |
80 |
80.9 |
78.6 |
|
Black |
11.2 |
9.8 |
12.3 |
14.3 |
|
Hispanic |
5 |
6.3 |
3.9 |
7.1 |
|
Asian/Pacific Islander |
0.7 |
1.1 |
0.4 |
0 |
|
Native American |
0.4 |
0.4 |
0.4 |
0 |
|
Other |
2.2 |
2.4 |
2.1 |
0 |
|
Gender |
|||||
Male |
46.1 |
49.7 |
43.1 |
45.8 |
|
Female |
53.9 |
50.3 |
56.9 |
54.2 |
|
Admission Type$ |
|||||
Elective |
13.3 |
13.8 |
12.8 |
16.9 |
|
Non-elective |
86.7 |
86.2 |
87.2 |
83.1 |
|
Charlson’s/Deyo Comorbidity Index@ |
|||||
0 |
49 |
48.9 |
49 |
57.6 |
|
1 |
22.9 |
22.8 |
22.9 |
18.6 |
|
2 |
12.3 |
11.8 |
12.7 |
11.9 |
|
>3 |
15.8 |
16.5 |
15.4 |
11.9 |
|
Primary Payer |
|||||
Medicare |
47 |
47.3 |
46.9 |
25.4 |
|
Medicaid |
8.8 |
7.1 |
10.2 |
18.6 |
|
Private Insurance (Including HMOs and PPOs) |
37.5 |
39.1 |
36.1 |
42.4 |
|
Self-Pay |
3.1 |
2.9 |
3.2 |
8.5 |
|
Other |
3.6 |
3.6 |
3.6 |
5.1 |
|
Median Household Income for Patient’s ZIP codej |
|||||
0-25 Percentile |
22.5 |
20.3 |
24.3 |
17.5 |
|
26-50 Percentile |
24.2 |
23.6 |
24.8 |
21 |
|
51-75 Percentile |
25.7 |
25.9 |
25.6 |
31.6 |
|
76-100 Percentile |
27.6 |
30.2 |
25.3 |
29.8 |
|
Teaching Status of Hospital |
|||||
Rural |
7.8 |
6.8 |
8.6 |
5.1 |
|
Urban (Non-teaching) |
37.2 |
37.5 |
37 |
28.8 |
|
Urban (Teaching) |
55 |
55.6 |
54.5 |
66.1 |
|
Hospital Region |
|||||
Northeast |
20.9 |
22.5 |
19.6 |
22 |
|
Midwest |
25 |
24 |
25.9 |
15.2 |
|
South |
35.7 |
32.7 |
38.2 |
32.2 |
|
West |
18.4 |
20.8 |
16.3 |
30.5 |
|
Disposition of Patient |
|||||
Routine |
52.1 |
50.5 |
53.3 |
52.5 |
|
Transfer to Short-term Hospital |
3.3 |
3.4 |
3.2 |
3.4 |
|
Transfer to Other$ |
19.7 |
22.3 |
17.7 |
13.6 |
|
Home Health Care |
19.5 |
17.6 |
21 |
28.8 |
|
Against Medical Advice |
0.6 |
0.4 |
0.8 |
0 |
|
Died |
4.7 |
5.7 |
3.9 |
1.7 |
|
Other: |
0.1 |
0.1 |
0.1 |
0 |
@- Charlson’s/Deyo comorbidity index was calculated as per Deyo classification.
ϕ- This represents a quartile classification of the estimated median household income of residents in the patient’s ZIP Code. These values are derived from ZIP Code-demographic data obtained from Claritas. The quartiles are identified by values of 1 to 4, indicating the poorest to wealthiest populations. Because these estimates are updated annually; the value ranges vary by year.
http://www.hcupus.ahrq.gov/db/vars/zipinc_qrtl/nisnote.jsp.
IBD- Inflammatory Bowel Disease, UC- Ulcerative Colitis, CD- Crohn’s Disease, HMO- Health Maintenance Organization, PPO- Preferred Provider Organization
Variable Name |
IBD (N=16550) |
UC (N=7422) |
CD (N=9069) |
Both (N=59) |
Diabetes Mellitus (uncomplicated) |
13.4 |
14.2 |
12.8 |
5.1 |
Diabetes Mellitus (with chronic complications) |
2.7 |
2.9 |
2.6 |
1.7 |
Hypertension |
39.7 |
41.8 |
38.1 |
27.1 |
Liver Disease |
4.5 |
5 |
4.1 |
1.7 |
Fluid and Electrolytes Disorder |
37.1 |
37.8 |
36.4 |
40.7 |
Other Neurological Disorder |
6.9 |
6.4 |
7.3 |
10.2 |
Obesity |
8.8 |
9.2 |
8.6 |
1.7 |
Peripheral Vascular Disease |
4.5 |
5.1 |
4 |
1.7 |
Valvular Disease |
3.7 |
3.8 |
3.7 |
1.7 |
Smoking |
16.2 |
12.6 |
19.2 |
11.9 |
Alcohol Abuse |
1.9 |
2.2 |
1.7 |
1.7 |
Coagulopathy |
9.8 |
10.5 |
9.2 |
13.5 |
Chronic Pulmonary Disease |
18.5 |
17.4 |
19.3 |
18.6 |
Congestive Heart Failure |
8.2 |
8.8 |
7.8 |
5.1 |
AIDS |
0.2 |
0.2 |
0.2 |
1.7 |
Deficiency Anemia |
31.6 |
30.1 |
32.9 |
37.3 |
Chronic Blood Loss Anemia |
5.1 |
6.5 |
3.9 |
6.8 |
Drug Abuse |
3 |
1.7 |
4 |
3.4 |
Renal Failure |
10.2 |
9.4 |
10.8 |
8.5 |
Peptic Ulcer Disease Excluding Bleeding |
0.1 |
0.1 |
0.1 |
0 |
Weight Loss |
18.3 |
18 |
18.5 |
16.9 |
Variable Name |
IBD (N=16550) |
UC (N=7422) |
CD (N=9069) |
Both (N=59) |
Active Fistulizing disease or intra-abdominal abscess |
7.1 |
4.4 |
9.3 |
10.2 |
Active Stricturing Disease |
2.6 |
1.3 |
3.7 |
1.7 |
Bowel Obstruction |
10.6 |
8 |
12.6 |
15.2 |
Perianal Abscess |
0.6 |
0.3 |
0.9 |
1.7 |
Unspecified Lower GI Bleeding |
5.2 |
6.1 |
4.4 |
10.2 |
Hypovolemia |
9.7 |
9.9 |
9.6 |
6.8 |
Malnutrition |
10.8 |
10.4 |
11.1 |
11.9 |
UC and CD cases were only available in 2014. Hence, we did not make a trend for that category.
IBD- Inflammatory Bowel Disease, UC- Ulcerative Colitis, CD- Crohn’s Disease
UC and CD cases were only available in 2014. Hence, we did not make a trend for that category.
IBD- Inflammatory Bowel Disease, UC- Ulcerative Colitis, CD- Crohn’s Disease
UC and CD cases were only available in 2014. Hence, we did not make a trend for that category. Trending down after surgeon general’s call to action in 2008 Abbreviations: IBD- Inflammatory Bowel Disease, UC- Ulcerative Colitis, CD- Crohn’s Disease
Surgeries Included for This Chart: Incision, Excision and Anastomosis of Intestine, Resection of Large Intestine, Rectal and perirectal Surgery, Other Surgery of small intestine, Other Surgery of large intestine, other surgery of intestine, unspecified site.
Variable Name |
2005 |
2006 |
2007 |
2008 |
2009 |
2010 |
2011 |
2012 |
2013 |
2014 |
Overall |
P value (Trend) |
Unweighted Population |
1167 |
1217 |
1282 |
1729 |
1771 |
1841 |
2021 |
1721 |
1846 |
1955 |
16550 |
N/A |
In-Hospital Mortality (Overall) |
2.57 |
3.29 |
3.51 |
5.9 |
4.8 |
5.21 |
5.64 |
4.88 |
4.93 |
4.4 |
4.67 |
0.005 |
Gender |
||||||||||||
Male |
1.28 |
1.48 |
1.4 |
2.7 |
2.5 |
2.3 |
2.6 |
2.3 |
2.3 |
1.9 |
2.2 |
0.1288 |
Female |
1.28 |
1.8 |
2.1 |
3.2 |
2.3 |
2.9 |
3 |
2.5 |
2.6 |
2.4 |
2.5 |
0.0157 |
Age |
||||||||||||
<35 |
0.1 |
0 |
0.1 |
0.2 |
0.2 |
0.3 |
0.2 |
0.3 |
0.1 |
0.1 |
0.2 |
0.4093 |
35-50 |
0.5 |
0.2 |
0.5 |
0.6 |
0.7 |
0.3 |
0.5 |
0.2 |
0.3 |
0.6 |
0.5 |
0.9366 |
50-65 |
0.5 |
0.6 |
0.8 |
1.3 |
0.9 |
1.7 |
1 |
1.5 |
0.2 |
0.9 |
1.1 |
0.072 |
65-80 |
0.5 |
1.7 |
0.8 |
2.8 |
1.9 |
1.5 |
2.6 |
2 |
2.2 |
1.8 |
1.9 |
0.0655 |
>80 |
0.9 |
0.6 |
1.2 |
0.9 |
1 |
1.4 |
1.3 |
0.9 |
1 |
0.9 |
1 |
0.5842 |
Race |
||||||||||||
White |
1.7 |
2.5 |
2.4 |
4.4 |
3.2 |
3.7 |
3.8 |
3.6 |
3.6 |
3.4 |
3.3 |
0.2623 |
Black |
0 |
0.3 |
0.3 |
0.3 |
0.6 |
0.6 |
0.8 |
0.5 |
0.3 |
0.2 |
0.4 |
0.7434 |
Other |
0.2 |
0.2 |
0.2 |
0.3 |
0.3 |
0.4 |
0.7 |
0.5 |
0.6 |
0.6 |
0.4 |
0.1144 |
Primary Payer |
||||||||||||
Medicare/Medicaid |
1.5 |
2.5 |
1.8 |
4 |
3.5 |
3.5 |
4.8 |
3.5 |
3.5 |
3.5 |
3.4 |
0.0127 |
Private Insurance (Including HMOs and PPOs) |
0.8 |
0.5 |
1.5 |
1.6 |
0.9 |
1.5 |
0.7 |
1 |
0.9 |
0.7 |
1 |
0.7299 |
Self-Pay/Other |
0.2 |
0.2 |
0.1 |
0.2 |
0.3 |
0.3 |
0.1 |
0.3 |
0.6 |
0.2 |
2.5 |
0.1169 |
Teaching Status of Hospital: |
||||||||||||
Rural |
0.3 |
0.1 |
0.2 |
0.5 |
0.3 |
0.4 |
0.2 |
0.3 |
0.4 |
0.2 |
0.3 |
0.1555 |
Urban (Non-teaching) |
1.1 |
1.1 |
1.3 |
2.1 |
1.8 |
2.3 |
2.3 |
1.3 |
1.5 |
0.8 |
1.6 |
0.0906 |
Urban (Teaching) |
1.2 |
2.1 |
1.9 |
3.3 |
2.4 |
2.5 |
2.9 |
3.3 |
3 |
3.3 |
2.7 |
0.108 |
Charlson’s/Deyo Comorbidity Index |
||||||||||||
0 |
0.8 |
0.9 |
1.1 |
1.7 |
1.5 |
1.8 |
1.5 |
1.7 |
1.4 |
1.3 |
1.4 |
0.0106 |
1 |
0.8 |
1 |
0.8 |
1.3 |
1.2 |
1.1 |
1.4 |
1.2 |
1.2 |
1.2 |
1.1 |
0.107 |
2 |
0.2 |
0.5 |
0.4 |
0.9 |
0.9 |
0.8 |
0.9 |
0.6 |
0.5 |
0.4 |
0.6 |
0.6032 |
>3 |
0.8 |
0.9 |
1.2 |
2 |
1.2 |
1.5 |
1.8 |
1.3 |
1.8 |
1.5 |
1.4 |
0.4 |
Variable Name |
Odds Ratio with 95% Confidence Interval |
P value (Wald’s) |
Age Groups |
||
<35 |
Referent |
|
35-50 |
1.973 (1.253-3.106) |
0.0033 |
50-65 |
3.220 (2.112-4.911) |
<0.0001 |
65-80 |
5.441 (3.485-8.497) |
<0.0001 |
>80 |
6.933 (4.367-11.007) |
<0.0001 |
Female vs Male |
0.956 (0.823-1.109) |
0.5516 |
Elective vs Non-Elective |
0.810 (0.637-1.030) |
0.0862 |
Primary Payer |
||
Medicare |
Referent |
|
Medicaid |
1.088 (0.758-1.560) |
0.6485 |
Private Including HMOs and PPOs |
0.819 (0.650-1.032) |
0.0909 |
Self-Pay/No-Charge/other |
1.282 (0.758-2.168) |
0.3551 |
Hospital Location |
||
Rural |
Referent |
|
Urban Non-teaching |
1.157 (0.847-1.581) |
0.3595 |
Urban Teaching |
1.429 (1.056-1.934) |
0.0277 |
Charlson’s/Deyo Comorbidity Index |
||
0 |
Referent |
|
1 |
1.396 (1.142-1.705) |
0.0011 |
2 |
1.330 (1.046-1.691) |
0.0201 |
>3 |
2.411 (1.987-2.925) |
<0.0001 |
In our study, majority of the population with VTE in IBD had low CCI index which proposed that IBD could be an independent risk factor for VTE as suggested in previous studies. But CCI>3 is strongly associated with higher mortality which demands screening for high risk for VTE in IBD population. Interestingly, our data suggest that there is higher rate of VTE in IBD at urban teaching hospitals. Our finding is consistent with the previous study that showed 14% - 15% high likelihood of having VTE in urban hospitals compared to rural hospitals [14]. It may be due to having more debilitated patients in urban tertiary centers who are at the greater risk for VTE.
Among the comorbidities, the most common was hypertension. It is associated with endothelial injury, a part of Virchow’s triad. Hypertension could be an independent risk factor for VTEs which may be mediated by the presence of inflammation. It is proven in recent study of newly diagnosed lung cancer patients [15]. Another significant comorbidity was fluid and electrolyte disorder which is common in IBD patients during flare. It could be due to inadequate oral intake. Dehydration is associated with hyper viscosity and ultimately increases risk of thrombosis. In recent study, dehydration is strongly associated with VTE after acute ischemic stroke [16, 17]. It should be further studied in IBD patients for a risk of VTE. Iron deficiency and anemia of chronic disease is also a well-known complication of IBD. It is due to the combination of malabsorption and chronic inflammatory state. It might be associated with increased risk of VTE in IBD. It should be investigated when anemia is a proven risk factor for VTE and cerebral venous thrombosis [17].
The most clinically relevant finding is the increasing VTE-associated mortality in IBD patients from 2005 to 2014. Although, IBD patients are younger and have less comorbid conditions, our finding shows an increase in twofold mortality. This finding may be an indication that VTEs are more severe in IBD patients. The rapidly rising rate of VTE in the hospitalized UC and CD population may be due to corticosteroid use and merits further exploration [18]. IBD related surgeries are unlikely the cause of mortality because the rate of VTE in IBD who required surgery has been decreased since 2008 as shown in chart 6. This may be due to efforts from office of surgeon general to prevent perioperative DVT and PE in 2008 [19]. With new biologic therapy thought to be associated with lower risk of VTE, it will need more studies [20]. Also, the rise in VTE rates may be attributable to advancement in diagnostic testing. Another possible explanation is that patients with UC and Crohn’s colitis may be more likely to have hematochezia and subsequently less likely to receive VTE prophylaxis.
Interestingly, it appears that UC patients with VTE have higher mortality compared to CD patients with VTE. This greater mortality among UC patients was previously suggested in a population-based study which could be explain further by higher colonic involvement and inflammation being a predisposing factor for VTE [21]. However, we do not have endoscopic data to comment on the role of severity of colonic inflammation. Supplementary studies are warranted to characterize the mechanisms of these associations. Our secondary outcomes include increased complication rate which could be attributing to the increased length of stay.
The increase in mortality for IBD patients with VTE emphasizes the potential benefit of adequate VTE prophylaxis. Further studies need to assess whether screening strategies for VTE in IBD patients. Despite reasonable awareness of the increased risk of thrombosis in hospitalized IBD patients, many clinicians may not follow clinical practice guidelines and use pharmacologic VTE prophylaxis [22]. Studies are warranted to measure the rate of VTE prophylaxis among hospitalized IBD patients. Even recent study shows that prophylactic anticoagulation is safe in IBD despite the presence of rectal bleeding on admission [23]. Thus, unless in the presence of hemodynamically significant GI bleeding, unfractionated or low-molecular weight heparin should not be contraindicated in either the treatment or prophylaxis of venous thrombosis. VTE is an increasingly prevalent and preventable complication of IBD and efforts toward early detection and therapy are essential in improving outcomes for IBD inpatients.
The large sample size of the NIS data set is a population-based representation of all hospitalized IBD patients in the United States and reflects all types of hospital settings, insurance payers, and geographic regions. Thus, the selected study population enhances the generalizability.
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