Abstract
Background
The development of Deep Vein Thrombosis (DVT) is a major concern following orthopaedic surgery. No study has yet to compare the rate and risk factors for DVT between total joint and orthopaedic trauma patients. To evaluate if DVT prophylaxis for trauma should differ from total joints, we explored the rate and risk factors for DVT between both cohorts.
Methods
Using a CPT code search from 2005 to 2013 in the ACS-NSQIP database, 150,657 orthopaedic total joint patients and 44,594 orthopaedic trauma patients were identified. DVT complications, patient demographics, preoperative comorbidities, and surgical characteristics were collected for each patient. A chi-squared test was used to compare the risk factors for DVT between orthopaedic trauma and total joint patients. A multivariable logistic regression model was built to adjust for comorbidities for each cohort.
Results
The rate of DVT diagnosis in the total joint population was 0.8% (N = 1186) and 0.98% (N = 432) in the orthopaedic trauma population (p = 0.57). After controlling for individual comorbidities, dyspnea, peripheral vascular disease, and renal failure were significant risk factors for DVT in total joint patients (p < 0.05), whereas age, ascites and steroid use were significant risk factors for DVT in orthopaedic trauma patients (p < 0.05).
Conclusions
Historically, the risks for DVT in total joints have been emphasized, yet based on our results, the incidence of DVT is the same for orthopaedic trauma. However, the risk factors varied. It is therefore important to consider specialty-specific DVT prophylaxis for orthopaedic trauma patients in order to improve care and reduce postoperative complications.
Keywords: Risk factor, Deep vein thrombosis, Total joint arthroplasty, Orthopaedic trauma, Prophylaxis
1. Introduction
Venous thromboembolism (VTE), including deep vein thrombosis (DVT) and pulmonary embolism (PE), remains a major concern following orthopaedic surgery, particularly since such disease is a leading cause of perioperative morbidity and mortality.1 Amongst patients hospitalized in the United States, it is the direct cause of death in more than 100,000 patients and a contributing factor of mortality in another 100,000 each year.2, 3 Several patient safety initiatives, such as the Agency for Healthcare Research and Quality Patient Safety Indicators, American Public Health Association’s Coalition to Prevent Deep Vein Thrombosis, and the US Surgeon General’s Workshop on Deep Vein Thrombosis have aimed to improve detection and prevention of VTE.4, 5, 6
To our knowledge, no study has yet to compare the risk factors for DVT between total joint and orthopaedic trauma patients. The purpose of this article is to identify the risk factors for DVT in trauma patients and compare to total joint patients through the use of prospective multicenter data in the American College of Surgeons National Surgical Quality Improvement Program (ACS-NSQIP) database. By evaluating the risk factors for DVT in each cohort, our study seeks to explore whether DVT prophylaxis guidelines for total joint patients can be applied to trauma surgery patients. As our health system transitions to bundle payments, it is essential for orthopaedic trauma surgeons to identify those patients most likely to experience thromboembolic complications in order to develop a cost effective DVT prevention program, specifically targeting those patients most at risk.
2. Methods
Patients undergoing orthopaedic procedures from 2005-2013 were identified in the ACS-NSQIP database using a Current Procedural Terminology (CPT) code search. Among these patients, a second CPT code search using only orthopaedic trauma “hip/pelvis” and “lower extremity (LE)” injury CPT codes was conducted to identify patients undergoing pelvis and LE orthopaedic trauma procedures. A similar CPT code search of total joint procedures established patients undergoing primary and revision total hip arthroplasty and primary and revision total knee arthroplasty. We chose to focus on lower extremity surgeries because they have previously been documented to have a higher incidence of DVT.7 Additionally, and more specifically, lower extremity and hip/pelvis orthopedic trauma patients have also been documented to have a higher incidence of DVT than upper extremity orthopedic trauma patients.8 Therefore we believe these patients would be most in need of new prophylaxis guidelines.
The development of a deep vein thrombosis (DVT) within 30-days following surgery was recorded for each patient. Patients with missing data were not included in the analysis. The ACS-NSQIP database we used encompasses over 300 variables including preoperative risk factors, intraoperative variable, and 30-day postoperative mortality and morbidity outcomes. After a careful literature review, we selected variables we believe to be most relevant to the development of DVT.9, 10, 11, 12, 13, 14, 15 Patient demographics (ASA Class, body mass index [BMI], sex, alcohol use, functional status and smoking status), preoperative comorbidities (ascites, bleeding disorder, ventilator use, diabetes, disseminated cancer, dyspnea, history of congestive heart failure [CHF], history of chronic obstructive pulmonary disorder [COPD], history of myocardial infraction [MI], dialysis, renal failure, use of steroids, preoperative sepsis, pneumonia, hypertension requiring medication, bleeding disorder, radiotherapy, peripheral vascular disease, and weight loss in the last 6 months), as well as operative characteristics (surgical duration, type of surgery for total joint patients, prior operation in last 30 days) were collected for each patient. Bivariate analyses using the chi-squared test and Wilcoxon-Mann-Whitney test were performed to compare risk factors between those who developed a DVT and those who did not for both the orthopaedic trauma and total joint cohorts. Statistical significance was set at α = 0.05.
A multivariate logistic regression was then conducted to determine the predictive risk factors for DVT development in orthopaedic trauma and in total joint patients.
3. Results
A total of 195,251 patients who underwent orthoapedic procedures were identified from 2005-2013 in the ACS-NSQIP datebase. Of these patients, 44,594 (22.8%) were orthopaedic trauma patients with pelvis and/or LE injuries and 150,657 (77.2%) were orthopaedic total joint patients. Of the total joint patients, 84,659 (56.2%) patients underwent primary total knee arthroplasty (TKA), 53,290 (35.4%) total hip arthroplasty (THA) and the remaining 12,708 patients (8.4%) underwent revision surgery.
As shown in Table 1, the incidence of DVT within 30 postoperative days for the total joint population [0.8% (n = 1186)] and for the orthopaedic trauma population [0.98% (N = 437)] did not significantly differ between the two groups (p = 0.57). For orthopaedic trauma patients, those who developed a DVT within 30-days following surgery had a significantly higher median age than those who did not: 80.0 (IQR: 69.0–87.0) years verses 77.0 (IQR: 59.0–86.0) years respectively (p < 0.01). A greater BMI (p = 0.017) and Caucasian race (p < 0.01) was also significantly associated with a higher rate of DVT development for orthopaedic trauma patients. Total joint patients who developed a DVT were also significantly older (p < 0.01), had a greater median BMI (p = 0.01), and were Caucasian (p < 0.01). Additionally, higher ASA scores for both orthopaedic trauma (p < 0.01) and total joint patients (p = 0.018) were significantly associated with an increased risk of DVT development.
Table 1.
Selected demographics for DVT for Trauma vs. Total Joint Patients.
Characteristic | Orthopaedic Trauma (n = 44,594) |
Total Joint (n = 150,657) |
||||
---|---|---|---|---|---|---|
DVT (n = 437, 0.98%) |
No DVT (n = 44157, 99.0%) |
p | DVT (n = 1186, 0.80%) |
NO DVT (n = 149471, 99.2%) |
p | |
Age (median, IQR) | 80.0 (69.0–87.0) | 77.0 (59.0–86.0) | <0.01 | 66.0 (59.0–74.0) | 68.0 (60.0–76.0) | <0.01 |
Gender (n,%) | 0.260 | 0.310 | ||||
Male | 141 (32.3%) | 15429 (35.0%) | 493 (41.57%) | 60098 (40.2%) | ||
Female | 296 (67.7%) | 28699 (65.0%) | 687 (57.9%) | 89134 (59.6%) | ||
Race (n,%) | <0.01 | <0.01 | ||||
White | 356 (81.5%) | 32286 (73.1%) | 914 (77.1%) | 120265 (80.5%) | ||
Black | 24 (5.5%) | 2316 (5.2%) | 113 (9.5%) | 9819 (6.6%) | ||
Other | 57 (13.0%) | 9555 (21.6%) | 159 (13.4%) | 19387 (13.0%) | ||
Functional Status | <0.01 | <0.01 | ||||
Independent | 310 (70.9%) | 33491 (75.8%) | 1133 (95.5%) | 144062 (96.4%) | ||
Partially dependent | 96 (22.0%) | 8498 (19.2%) | 38 (3.20%) | 4340 (2.90%) | ||
Dependent | 28 (6.4%) | 1761 (4.0%) | 7 (0.60%) | 262 (0.2%) | ||
Unknown | 3 (0.70%) | 407 (0.92%) | ||||
BMI (median, IQR) | 25.2 (21.5-29.2) | 24.7 (20.6–29.2) | 0.017 | 31.2 (27.4–35.8) | 30.6 (26.6–35.5) | <0.01 |
Smoke (n,%) | 57 (13.0%) | 7318 (16.0%) | 0.056 | 115 (9.70%) | 15922 (10.7%) | 0.310 |
Alcohol use (n,%) | 7 (1.6%) | 751 (1.7%) | 0.999 | 8 (0.70%) | 1369 (0.92%) | 0.320 |
ASA score (n,%) | <0.01 | <0.01 | ||||
1 | 14 (3.2%) | 3074 (7.0%) | 21 (1.77%) | 4274 (2.86%) | ||
2 | 88 (20.1%) | 12138 (27.5%) | 540 (45.5%) | 76949 (51.5%) | ||
3 | 242 (55.4%) | 22775 (51.6%) | 588 (49.6%) | 65065 (43.5%) | ||
4 | 93 (21.3%) | 6170 (14.0%) | 34 (2.87% | 3013 (2.02%) | ||
5 | 0 (0.0%) | 0 (0.0%) | 0 (0.0%) | 9 (0.01%) |
Bold values are significant (p < 0.05).
As shown in Table 2, the incidence of DVT significantly differed based on preoperative comorbidities and operative characteristics. For the trauma cohort, the rate of DVT was significantly higher if the patient had ascites (p < 0.01), a history of dyspnea (p = 0.034), a history of hypertension requiring medication (p < 0.01), preoperative renal failure (p < 0.01), preoperative steroid use (p = 0.048), a bleeding disorder (p = 0.05), or had preoperative sepsis (p = 0.01). Previous operations in the past 30 days (p < 0.01) and use of a ventilator (p < 0.01) also increased the rate of DVT in trauma patients. For the total joint cohort, a history of dyspnea (p = 0.020), ascites (p = 0.045), a history of hypertension requiring medication (p = 0.01), bleeding disorders (p = 0.01), and preoperative sepsis (p < 0.01) presented with a higher rate of DVT 30-days post-operation.
Table 2.
Preoperative Comorbidities and Operative Characteristics for DVT for Trauma vs. Total Joint Patients.
Characteristic | Orthopaedic Trauma (n = 44,594) |
Total Joint (n = 150,657) |
||||
---|---|---|---|---|---|---|
DVT (n = 437, 0.98%) |
No DVT (n = 44157, 99.0%) |
p | DVT (n = 1186, 0.80%) |
NO DVT (n = 149,471, 99.2%) |
p | |
Ascites | 6 (1.4%) | 95 (0.22%) | <0.01 | 2 (0.20%) | 41 (0.03%) | 0.045 |
Diabetes (Insulin dependent) | 41 (9.4%) | 3484 (8.0%) | 0.200 | 52 (4.40%) | 5733 (3.84%) | 0.360 |
Dyspnea at rest | 10 (2.3%) | 505 (1.1%) | 0.034 | 5 (0.42%) | 414 (0.28%) | 0.020 |
Ventilator | 5 (6.8%) | 73 (0.98%) | <0.01 | 0 (0.0%) | 16 (0.01%) | 0.999 |
Hx COPD | 41 (9.4%) | 3965 (9.0%) | 0.834 | 55 (4.64%) | 5958 (3.99%) | 0.290 |
Hx CHF | 13 (3.0%) | 1135 (2.6%) | 0.704 | 6 (0.50%) | 468 (0.30%) | 0.360 |
Hypertension | 298 (68.2%) | 25525 (57.8%) | <0.01 | 797 (67.2%) | 94017 (62.90%) | <0.01 |
Hx MI | 3 (0.70%) | 192 (0.43%) | 0.640 | 2 (0.20%) | 55 (0.04%) | 0.150 |
Pneumonia | 2 (0.50%) | 115 (0.26%) | 0.720 | 0 (0.0%) | 18 (0.01%) | 0.999 |
Disseminated cancer | 22 (5.0%) | 1111 (2.5%) | 0.305 | 4 (0.34%) | 347 (0.23%) | 0.660 |
Steroid use | 35 (8.0%) | 2017 (4.6%) | <0.01 | 52 (4.38%) | 5148 (3.44%) | 0.090 |
Bleeding disorder | 69 (15.8%) | 5546 (12.6%) | 0.050 | 54 (4.60%) | 4518 (3.02%) | <0.01 |
Dialysis dependent | 11 (2.5%) | 828 (1.9%) | 0.420 | 3 (0.25%) | 337 (0.23%) | 0.999 |
Renal Failure | 9 (2.1%) | 260 (0.59%) | <0.01 | 2 (0.20%) | 80 (0.05%) | 0.290 |
Receiving radiotherapy | 4 (0.92%) | 92 (0.21%) | <0.01 | 0 (0.0%) | 31 (0.02%) | 0.999 |
Peripheral Vascular disease | 3 (0.70%) | 564 (1.3%) | 0.400 | 6 (0.51%) | 312 (0.21%) | 0.090 |
Preoperative sepsis | 11 (2.5%) | 556 (1.3%) | <0.01 | 9 (0.76%) | 261 (0.17%) | <0.01 |
Weight loss in last 6 months | 10 (2.3%) | 510 (1.2%) | 0.048 | 3 (0.25%) | 389 (0.26%) | 0.999 |
Operative characteristics | ||||||
Prior Operation within 30 days | 14 (3.2%) | 429 (0.97%) | <0.01 | 7 (0.59%) | 306 (0.20%) | 0.018 |
Operative time minutes (median, IQR) | 73.0 (49.0–108.0) | 65.0 (44.0–95.0) | <0.01 | 93 (72–120) | 90 (71–117) | 0.010 |
Bold values are significant (p < 0.05).
After controlling for all individual patient factors, the risk factors associated with DVT development differed between total joint and orthopaedic trauma patients as demonstrated in Table 3. Age was found to be a significant risk factor for DVT for orthopaedic trauma patients (OR: 1.02, 95% CI: 1.00–1.03, p = 0.01) whereas it was not a significant risk factor for total joint patients (p = 0.083). Unlike a total joint patient, a trauma patient with ascites was 5.14 times (95% CI: 1.04–35.4, p = 0.04) more likely to develop a DVT. Steroid use was also found to be a significant predictor of DVT in trauma patients but not in total joint patients. A history of peripheral vascular disease was associated with a significant 3.30 increased risk of DVT for total joint patients (95% CI: 1.13–9.55, p = 0.03) whereas it was not shown to be a risk factor for trauma patients. Dyspnea at rest increased the risk of DVT by 4.25 times (95% CI: 1.05–17.2, p = 0.43) and renal failure increased the risk by 12.3 times (95% CI: 1.4–107.4, p = 0.024) for total joint patients. For trauma patients, renal failure was shown to increase the risk of DVT by 2.46 times and was not found to be significant (p = 0.12). Additionally, an operation in the 30-days prior to surgery was found to be a significant risk factor for both cohorts, increasing the risk of DVT by 5.23 times (95% CI: 1.83–15.0, p = 0.002) for total joint patients and 3.93 times (95% CI: 2.10–7.33, p < 0.01) for trauma patients.
Table 3.
Comparison of risk factors for DVT between Trauma vs. Total Joints.
Risk factor | Orthopaedic trauma (n = 22,361) |
Total Joint |
||||
---|---|---|---|---|---|---|
Odds ratio | 95% confidence interval | p | Odds ratio | 95% confidence interval | p | |
Patient Demographics | ||||||
Age | 1.02 | 1.00–1.03 | <0.01 | 1.02 | 1.00–1.03 | 0.083 |
Gender | ||||||
Female | Reference | – | – | Reference | – | – |
Male | 1.11 | 0.76–1.63 | 0.580 | 0.93 | 0.66–1.31 | 0.669 |
Race | ||||||
White | Reference | – | – | Reference | – | – |
Black | 0.85 | 0.43–1.67 | 0.630 | 1.56 | 0.93–2.62 | 0.095 |
Functional Status | ||||||
Independent | Reference | – | – | Reference | – | – |
Dependent | 1.39 | 0.74–2.63 | 0.305 | 0.50 | 0.02–12.00 | 0.675 |
BMI | 1.01 | 0.99–1.03 | 0.425 | 1.00 | 0.98–1.02 | 0.950 |
Smoke | 0.96 | 0.56–1.64 | 0.872 | 1.03 | 0.58–1.82 | 0.930 |
Alcohol | 1.54 | 0.69–3.48 | 0.294 | 1.51 | 0.60–3.79 | 0.380 |
ASA score | ||||||
1 | Reference | – | – | Reference | – | – |
2 | 1.60 | 0.47–5.50 | 0.454 | 1.19 | 0.28–4.97 | 0.820 |
3 | 1.54 | 0.43–5.54 | 0.505 | 1.57 | 0.37–6.72 | 0.540 |
4 | 1.46 | 0.37–5.73 | 0.585 | 1.94 | 0.34–11.00 | 0.450 |
Preoperative Comorbidities | ||||||
Ascites | 5.14 | 1.04–25.40 | 0.044 | 0.00 | – | 0.978 |
Diabetes (Insulin dependent) | 1.27 | 0.72–2.23 | 0.410 | 1.18 | 0.56–2.45 | 0.666 |
Dyspnea at rest | 1.67 | 0.60–4.63 | 0.324 | 4.25 | 1.05–17.23 | 0.043 |
Ventilator | 3.34 | 0.36–30.70 | 0.286 | 0.00 | – | 0.936 |
Hx COPD | 0.62 | 0.32–1.22 | 0.165 | 0.53 | 0.20–1.40 | 0.200 |
Hx CHF | 0.98 | 0.34–2.80 | 0.963 | 0.77 | 0.03–17.70 | 0.870 |
Hypertension | 1.17 | 0.77–1.77 | 0.465 | 1.01 | 0.69–1.49 | 0.940 |
Hx MI | 1.92 | 0.61–6.03 | 0.750 | 3.68 | 0.37–36.80 | 0.270 |
Pneumonia | 0.97 | 0.21–4.50 | 0.970 | 0.00 | – | 0.934 |
Disseminated cancer | 1.70 | 0.63–4.60 | 0.293 | 0.00 | – | 0.890 |
Steroid use | 2.00 | 1.07–3.75 | 0.031 | 1.35 | 0.57–3.18 | 0.420 |
Bleeding disorder | 1.03 | 0.62–1.73 | 0.902 | 1.14 | 0.51–2.56 | 0.755 |
Dialysis dependent | 1.04 | 0.35–3.12 | 0.950 | 0.00 | – | 0.890 |
Renal Failure | 2.46 | 0.80–7.54 | 0.117 | 12.25 | 1.40–107.4 | 0.024 |
Receiving radiotherapy | 1.18 | 0.22–6.24 | 0.845 | 0.00 | – | 0.932 |
Peripheral Vascular disease | 0.40 | 0.12–1.33 | 0.134 | 3.29 | 1.13–9.55 | 0.029 |
Preoperative sepsis | 2.24 | 0.93–5.40 | 0.073 | 0.00 | – | 0.909 |
Weight loss in last 6 months | 1.98 | 0.68–5.75 | 0.209 | 2.92 | 0.61–13.96 | 0.180 |
Operative Characteristics | ||||||
Prior Operation within 30 days | 3.93 | 2.10–7.33 | <0.01 | 5.23 | 1.83–14.97 | 0.002 |
Operative time minutes | 1.00 | 1.00–1.01 | 0.065 | 1.01 | 1.00–1.01 | <0.01 |
Bold values are significant (p < 0.05).
4. Discussion
Our study, based on multicenter prospective data of over 195,000 patients, is the first to compare the incidence and risk factors for DVT in orthopaedic trauma and total joint populations. The incidence for DVT in the first 30 days after surgery for trauma and joint patients was comparable, measuring 0.98% and 0.8% respectively. Nonetheless, risk factors for DVT differed between the groups in several important categories. Increased age, steroid use and preoperative ascites were independent risk factors for DVT in the trauma group but did not significantly influence outcomes in the total joint group. Likewise, patient comorbidities such as dyspnea at rest, renal failure and peripheral vascular disease increased the incidence of thromboembolic events in total joint patients but did not play a significant role in the trauma patient cohort.
DVT after surgery is costly from both a social and economic standpoint. DVT increases length of hospital stay, medical costs and overall mortality.16, 17 For these reasons, much attention has been paid to developing strategies to prevent thromboembolic events. Perhaps the greatest strides in forming standardized guidelines for chemoprophylaxis have come in the area of total joint arthroplasty.18 Guidelines from the American Academy of Orthopaedic Surgeons (AAOS) and the American Collage of Chest Physicians (ACCP) have led to lower incidence of clinically significant DVTs in joint replacement patients.19, 20 This success has led many to apply these recommendations to orthopaedic patients as a whole. Our results suggest that risk factors for DVT in total joint patients differ from those of trauma patients.
The use of chemoprophylaxis in the setting of multi-injured trauma patients is not without dangers and limitations. Chemical DVT prophylaxis may be contraindicated in patients with brain or spinal cord injury over concern for hemorrhage. Patients requiring multiple successive procedures or those who are coagulopathic may not benefit from the use of chemical prophylaxis in the acute setting. Mechanical prophylaxis may be impractical in patients with lower extremity injuries. Thus, any generalized guideline for DVT prophylaxis must take into account the complexities associated with caring for trauma patients. The system of bundled payments must also take into account these difficulties when assessing adverse events and financial compensation.
Our study has several limitations. First, we were constrained by the data points recorded in the NSQIP database. Other risk factors, not recorded by investigators, may play a role in the development of DVT, thus confounding our results. Second, use of large databases relies on accurate CPT coding and data entry. Inaccuracies in data entry will confound results. Perhaps most significant to our study is the lack of standardization in DVT prophylaxis across institutions and surgeons involved in NSQIP. Treatments range from mechanical prophylaxis to varying chemical prophylaxis including antithrombin agents, anti-platelets and factor X inhibitors. Currently, the optimal DVT prophylaxis strategy is still unknown.21, 22 The effect of differing prophylaxis regimens could have influenced our results. Additionally, NSQIP data does not distinguish between isolated and multi-extremity injuries. Therefore it was not possible to separate polytrauma patients from the cohort. A high injury severity score (ISS) has been found to be an independent risk factor for VTE, including DVTs.23 In our study, ascites was an independent risk factor for DVT in the trauma patient cohort. This may be a surrogate for patients with a high ISS, developing traumatic ascites after massive fluid resuscitation.24
DVT prophylactic guidelines have been successful at reducing thromboembolic events in arthroplasty patients. One must use caution when attempting to apply such recommendations to orthopaedic trauma patients. The findings of our study indicate that risk factors for DVT in trauma patients differ from those of the joint patient population. Further research is needed to elucidate which subset of trauma patients are most at risk for a thromboembolic event and will benefit from chemical and mechanical prophylaxis.
Conflict of Interest Statement
Author William Obremskey has previously consulted for biometrics; done expert testimony in legal matters, has a grant from the Department of Defense, and has been a Board Member of the OTA and SEFC. For the remaining authors, no conflicts of interest are declared.
Ethical Review Committee Statement
This study was performed in accordance with the relevant regulations of the US Health Insurance Portability and Accountability Act (HIPPA) and the ethical standards of the 1964 Declaration of Helsinki. The protocol was approved by the Vanderbilt Institution Review Board.
Acknowledgement
None.
References
- 1.Abelseth G., Buckley R.E., Pineo G.E. Incidence of deep-vein thrombosis in patients with fractures of the lower extremity distal to the hip. J Orthop Trauma. 1996;10:230–235. doi: 10.1097/00005131-199605000-00002. [DOI] [PubMed] [Google Scholar]
- 2.Anderson F.A., Spencer F.A. Four topics in venous thromboembolism: risk factors for venous thromboembolism. Circulation. 2003;107 doi: 10.1161/01.CIR.0000078469.07362.E6. I-9–I-16. [DOI] [PubMed] [Google Scholar]
- 3.Dalen J.E., Alpert J.S. Natural history of pulmonary embolism. Prog Cardiovasc Dis. 1975;17:259–270. doi: 10.1016/s0033-0620(75)80017-x. [DOI] [PubMed] [Google Scholar]
- 4.Agency for Healthcare Research and Quality (AHRQ) Quality indicators: Guide to Patient Safety Indicators [AHRQ quality indicators]. http://www.qualityindicators.ahrq.gov/Modules/psi_resources.aspx. Accessed 20 March 2015.
- 5.Coalition to Prevent Deep Venous Thrombosis [Association APH]. http://www.apha.org/programs/partnerships/dvt.htm. Accessed 20 March 2015.
- 6.Office of the Surgeon General (US), National Heart, Lung, and Blood Institute (US) Office of the Surgeon General (US); Rockville (MD): 2008. The Surgeon General's Call to Action to Prevent Deep Vein Thrombosis and Pulmonary Embolism. [PubMed] [Google Scholar]
- 7.Rico J., Pitarch J., Rocha E. Overview of venous thromboembolism. Drugs. 2010;70(2):3–10. doi: 10.2165/1158583-S0-000000000-00000. [DOI] [PubMed] [Google Scholar]
- 8.Whiting P.S., White-Dzuro G.A., Greenberg S.E. Risk factors for deep venous thrombosis following orthopaedic trauma surgery: an analysis of 56,000 patients. Arch Trauma Res. 2016;5(1):e32915. doi: 10.5812/atr.32915. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Zhang H., Mao P., Wang C. Incidence and risk factors of deep vein thrombosis (DVT) after total hip or knee arthroplasty: a retrospective study with routinely applied venography. Blood Coagul Fibrinolysis. 2016 doi: 10.1097/MBC.0000000000000556. Epud ahead of print. [DOI] [PubMed] [Google Scholar]
- 10.Michetti C.P., Franco E., Coleman J., Bradford A., Trickey A.W. Deep vein thrombosis screening and risk factors in a high-risk trauma population. J Surg Res. 2015;199(2):545–551. doi: 10.1016/j.jss.2015.04.069. [DOI] [PubMed] [Google Scholar]
- 11.Wakabayashi H., Hasegawa M., Niimi R., Sudo A. Clinical analysis of preoperative deep vein thrombosis risk factors in patients undergoing total hip arthroplasty. Thromb Res. 2015;136(5):855–858. doi: 10.1016/j.thromres.2015.06.021. [DOI] [PubMed] [Google Scholar]
- 12.Kang J., Jiang X., Wu B. Analysis of risk factors for lower-limb deep venous thrombosis in old patients after knee arthroplasty. Chin Med J (Engl) 2015;128(10):1358–1362. doi: 10.4103/0366-6999.156782. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Lee S.Y., Ro Du H., Chung C.Y. Incidence of deep vein thrombosis after major lower limb orthopedic surgery: analysis of a nationwide claim registry. Yonsei Med J. 2015;56(1):139–145. doi: 10.3349/ymj.2015.56.1.139. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Decker S., Weaver M.J. Deep venous thrombosis following different isolated lower extremity fractures: what is known about prevalences, locations, risk factors and prophylaxis? Eur J Trauma Emerg Surg. 2013;39(6):591–598. doi: 10.1007/s00068-013-0266-6. [DOI] [PubMed] [Google Scholar]
- 15.Paffrath T., Wafaisade A., Lefering R. Venous thromboembolism after severe trauma: incidence, risk factors, and outcome. Injury. 2010;41(1):97–101. doi: 10.1016/j.injury.2009.06.010. [DOI] [PubMed] [Google Scholar]
- 16.Lefebvre P.1, Laliberté F., Nutescu E.A. All-cause and potentially disease-related health care costs associated with venous thromboembolism in commercial, medicare, and medicaid beneficiaries. J Manag Care Pharm. 2012;18(June (5)):363–374. doi: 10.18553/jmcp.2012.18.5.363. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.Gangireddy C.1, Rectenwald J.R., Upchurch G.R., Wakefield T.W., Khuri S., Henderson W.G. Risk factors and clinical impact of postoperative symptomatic venous thromboembolism. J Vasc Surg. 2007;45(February (2)):335–341. doi: 10.1016/j.jvs.2006.10.034. Discussion 341–342. [DOI] [PubMed] [Google Scholar]
- 18.Jacobs J.J., Mont M.A., Bozic K.J. American Academy of Orthopaedic Surgeons clinical practice guideline on preventing venous thromboembolic disease in patients undergoing elective hip and knee arthroplasty. J Bone Joint Surg Am. 2012;94:746–747. doi: 10.2106/JBJS.9408.ebo746. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Lewis C.G., Inneh I.A., Schutzer S.F., Grady-Benson J. Evaluation of the first-generation AAOS clinical guidelines on the prophylaxis of venous thromboembolic events in patients undergoing total joint arthroplasty: experience with 3289 patients from a single institution. J Bone Joint Surg Am. 2014;96(August (16)):1327–1332. doi: 10.2106/JBJS.M.00503. [DOI] [PubMed] [Google Scholar]
- 20.Falck-Ytter Y., Francis C.W., Johanson N.A. 9th ed. American College of Chest Physicians evidence-based clinical; 2012. Prevention of VTE Orthopedic Surgery Patients: Antithrombotic Therapy and Prevention of Thrombosis. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Toker S., Hak D.J., Morgan S.J. Deep vein thrombosis prophylaxis in trauma patients. Thrombosis. 2011;2011:505373. doi: 10.1155/2011/505373. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Sheth N.P., Lieberman J.R., Della Valle C.J. DVT prophylaxis in total joint reconstruction. Orthop Clin North Am. 2010;41(2):273–280. doi: 10.1016/j.ocl.2010.02.001. [DOI] [PubMed] [Google Scholar]
- 23.Paffratha Thomas, Wafaisadea Arasch, Lefering Rolf. Venous thromboembolism after severe trauma: incidence, risk factors and outcome. Injury. 2010;41(January (1)):97–101. doi: 10.1016/j.injury.2009.06.010. [DOI] [PubMed] [Google Scholar]
- 24.Mayberry J.C., Welker K.J., Goldman R.K., Mullins R.J. Mechanism of acute ascites formation after trauma resuscitation. Arch Surg. 2003;138(July (7)):773–776. doi: 10.1001/archsurg.138.7.773. [DOI] [PubMed] [Google Scholar]