Introduction
Liver cirrhosis is a major health problem worldwide, especially in Saudi Arabia[
1] where the prevalence of liver cirrhosis is not precisely known but is expected to be high due to the relatively high prevalence of viral hepatitis[
2‐
4]. Liver cirrhosis is accompanied by multiple changes in the hemostatic system due to the reduced levels of natural inhibitors of coagulation and coagulation factors because of the impaired hepatic synthetic activity [
5]. Thus, the global effect of liver disease on hemostasis is complex, and therefore, patients with liver cirrhosis can experience bleeding or thrombotic complications [
6]. The pathogenesis of venous thromboembolism (VTE) in cirrhosis is complex and involves several factors, both endogenous changes associated with cirrhosis with increased levels of factors VII and also protein C activity is limited in the absence of the endothelial receptor thrombomodulin and therefore it cannot exert its full anti-coagulant activity as well as external factors, one of which is limited physical activity due to the disease itself [
7‐
10]. The incidence of VTE among high-risk hospitalized patients has been reported to range between 4 and 12%[
7]. In a large necropsy series, in which fatal VTE accounted for 7-10% of all hospital-related deaths, 70-90% of the patients had no premorbid symptoms [
11]. Among these subjects with VTE, approximately 25% died within 7 days of VTE onset[
12]. In addition, the American College of Chest Physicians (ACCP) guidelines on VTE prophylaxis do not specifically address patients with coagulopathy due to liver cirrhosis [
13]. Based on the presence of coagulopathy in cirrhotic patients, these patients are considered to be auto-anticoagulant[
14]. Hence, the institution of deep vein thrombosis (DVT) prophylaxis in cirrhotic patients may not be a standard practice, and the use of DVT prophylaxis in this patient population is expected to be variable.
The objective of the present study was to determine the incidence and predictors of VTE and to examine the practice of DVT prophylaxis among hospitalized cirrhotic patients.
Methods
Study population
A retrospective chart review was conducted of patients with discharge ICD-9 diagnosis codes corresponding to liver cirrhosis who were admitted to a tertiary care hospital in Riyadh, Saudi Arabia, from January 1, 2009 to December 31, 2009. These patients were adults of 18 years or older and had a history and clinical presentation consistent with liver cirrhosis and/or a liver biopsy showing cirrhosis. Patients on anticoagulation therapy were excluded from the study. The study was approved by King Abdullah International Medical Research Center and the institutional review board of the hospital (IRB). The approval allowed for a retrospective chart review without informed consent.
Data collection
For each patient, the following information was collected: age, gender, admission creatinine, international normalized ratio (INR), bilirubin, albumin and platelet counts, etiology of liver cirrhosis (viral hepatitis, alcohol, autoimmune, cryptogenic), Child-Pugh score, VTE risk factors (history of malignancy, prior VTE, hormonal replacement therapy, oral contraceptives), use of pharmacologic prophylaxis in the form of unfractionated heparin (UFH) or low molecular-weight heparin (LMWH) and the use of mechanical prophylaxis. Patients were followed up until discharge from the hospital or until death, whichever was earlier.
Outcome measures
The primary outcome was defined as the development of symptomatic DVT or PE, as confirmed by venous Doppler ultrasound (VD-US) of the lower limbs, spiral CT of the chest or a high probability ventilation-perfusion (VQ) scan. These tests were ordered by the treating physician based on clinical suspicion. The secondary outcome was the use of DVT prophylaxis.
Statistical analysis
Continuous data were compared using the Kruskal-Wallis test and are expressed as the median and Interquartile range according to normality testing using Kolmogorov-Smirnov test. Categorical data were compared using the chi-square test or Fisher's exact test and are expressed as a percentage. Statistical significance was defined as alpha less than 0.05. Statistical analysis was performed using Minitab for Windows (release 13.1).
Discussion
The incidence of VTE was 2.7% in hospitalized cirrhotic patients, where the VTE evaluations were performed based on clinical suspicion. The majority of patients (76.1%) received neither pharmacological nor mechanical DVT prophylaxis. The underlying coagulopathy observed in cirrhotic patients has led to the notion that these patients might be at a lower risk for VTE [
7,
15]. This hypothesis was suggested in a population-based case-control study[
12] performed in the last century, which found that serious liver disease was associated with a 90% reduction in the risk for VTE. However, that study lacked the data on the severity of the liver diseases, use of DVT prophylaxis, and the diagnosis of VTE was not performed using the standard practices [
12]. However, the specific insight is inconsistent with the results of many studies that have addressed the incidence of VTE in cirrhotic patients. Recently a Danish nationwide population- base case- control study [
9] showed that the liver cirrhosis was associated with increased relative risk of VTE; 1.74 (95% CI,1.54-1.95) and in patients with unprovoked VTE, relative risk was slightly higher; 2.06(95% CI,1.79-2.38, regardless of the presence of other risk factors. A case-control study[
16] showed that the prevalence of DVT in cirrhotic patients was 4.7% and that diabetes mellitus was an independent risk factor for the development of DVT, which were not found in the present study. Northup et al. [
17]conducted a retrospective cohort study over an 8-year period and determined an incidence of VTE among 21,000 cirrhotic patients (in whom alcohol was the most frequent underlying etiology) of 0.5%, which had lower incidence of VTE (4 to 12%) found in selected subgroups of patients at the same institution. They also found that a low serum albumin level was an independent predictor of VTE in cirrhotic patients and that 79% of cirrhotic patients received neither pharmacological nor mechanical DVT prophylaxis, which is similar to the rate observed in our study. Another case-control study by Gulley et al. [
7] found 1.8% incidence of VTE and the risk for VTE was not lower than that determined for matched non-cirrhotic controls without selected co-morbidities, a finding similar to our study. Dabbagh et al[
14]. found an incidence of VTE of 6.3% in cirrhotic patients, and although the utilization of DVT prophylaxis was suboptimal, there was no association between the incidence of VTE and prophylaxis. The high incidence of VTE could be explained by the greater morbidity of these patients, as reflected by their high child-Pugh scores. The failure of DVT prophylaxis should be interpreted with caution, because the low VTE incidence and low rate of DVT prophylaxis utilization preclude the establishment of firm conclusions. Our result and others [
7,
16,
17] showed that the incidence of VTE was not lower than that determined in matched non-cirrhotic patients, even in patients with cirrhosis of different etiologies and with varying levels of severity.
Several mechanisms have been proposed to explain the observed thrombosis in cirrhotic patients. An acquired deficiency of antithrombotic III, protein C and protein S and the presence of antiphospholipid antibodies are observed in patients with cirrhosis [
5,
18,
19]. In addition to a decreased synthesis of anticoagulants, cirrhotic patients are prone to hypercoagulation due to a chronic inflammatory state that results in poor flow and vasculopathy [
16,
20]. Lisman et al[
21] found thrombin generation is equal or superior in patients with liver cirrhosis undergoing liver transplantation compared to healthy volunteers in the presence of exogenous thrombomodulin. An imbalance between the hemostatic process, thrombosis may produce a prothrombotic state in which the risk of thrombosis is increased [
22]. Our study has several limitations that are unavoidable in a retrospective study. It was conducted in one center where the sample size was relatively small. In addition, some of the variables extracted from the medical charts (such as patient lifestyle) were not available, which could confound our results as well as the suspecting PE is very low as reflected by the fact that only one spiral CT of chest was done. Despite these potential weaknesses, few studies have addressed this issue, and there are no guidelines regarding DVT prophylaxis in hospitalized cirrhotic patients. The present study elucidates possible predictors of the risk for VTE in this group of patients and may aid in determining the patients who will benefit from DVT prophylaxis, despite the notion that auto-anticoagulation protects against VTE in cirrhotic patients[
17]. These data will pave the way for further studies designed to evaluate the role of DVT prophylaxis in cirrhotic patients and alert healthcare providers to consider VTE in the differential diagnosis of cirrhotic patients with coagulopathy when these patients present with clinical features that are compatible with VTE.
Until the risks and benefits of VTE prophylaxis are established in this particular population, the VTE prophylaxis can not be withdrawn in the cirrhotic population at present time[
23].
In conclusion, the incidence of VTE in hospitalized cirrhotic patients was 2.7%, and the utilization of DVT prophylaxis was suboptimal. Because the treatment and prophylaxis for VTE carries an increased risk of bleeding, additional prospective multicenter studies should be conducted to address the benefits and risks of this intervention.
Competing interests
The authors declare that they have no competing interests.
Authors' contributions
AAL: carried out the design, interpretation, statistical analysis, drafting of the manuscript and critical revision of the manuscript
YA: carried out the design, statistical analysis and critical revision of the manuscript
AJ: carried out the design, interpretation, and drafting of the manuscript
AA: carried out the data collection, the design, interpretation and drafting of the manuscript
AR: carried out the data collection, the design, statistical analysis, interpretation and drafting of the manuscript
HD: carried out the design, interpretation and critical revision of the manuscript
SQ: carried out the design, statistical analysis and critical revision of the manuscript
MS: carried out the design, statistical analysis and critical revision of the manuscript
AF: carried out the design, statistical analysis and critical revision of the manuscript
All authors read and approved the final manuscript