Risk Factors for Clinically Relevant Pulmonary Embolism and Deep Venous Thrombosis in Patients Undergoing Primary Hip or Knee Arthroplasty
Mantilla, Carlos B. M.D., Ph.D.*; Horlocker, Terese T. M.D.†; Schroeder, Darrell R. M.S.‡; Berry, Daniel J. M.D.§; Brown, David L. M.D.#
Background: Prevention of thromboembolic complications after elective lower extremity arthroplasty has increasingly relied on routine thromboprophylaxis in all patients. Not all patients are at equal risk, however, and prophylaxis is not devoid of complications. The aim of this study was to examine the risk factors for clinically relevant pulmonary embolism and deep venous thrombosis after elective primary hip or knee arthroplasty in a large patient population.
: During the 10-yr study period, 116 of 9,791 patients undergoing primary hip or knee arthroplasty at the authors’ institution who experienced pulmonary embolism or deep venous thrombosis within 30 days of surgery were matched at a 1:1 ratio with patients undergoing the same surgery with the same surgeon who did not experience an adverse event. Medical records were reviewed, with data abstracted using a standardized data collection form.
: Increased body mass index (P
= 0.031; odds ratio = 1.5 for each 5-kg/m2
increase) and American Society of Anesthesiologists physical status classification of 3 or greater (P
= 0.005; odds ratio = 2.6) were found to independently increase the likelihood of pulmonary embolism or deep venous thrombosis. In addition, use of antithrombotic prophylaxis was found to decrease the likelihood of these thromboembolic events (P
= 0.050; odds ratio = 0.2 for aspirin or subcutaneous heparin, and odds ratio = 0.4 for warfarin or low-molecular-weight heparin).
Conclusions: In patients undergoing primary elective lower extremity arthroplasty, obesity, poor American Society of Anesthesiologists physical status classification, and lack of thromboprophylaxis are independent risk factors for clinically relevant thromboembolic events.
A LARGE number of studies have examined the incidence of thromboembolic complications after lower extremity orthopedic surgery. 1–4
Early studies reported a high frequency of symptomatic deep venous thrombosis and pulmonary embolism in patients after hip or knee arthroplasty. 5,6
More recent studies have demonstrated a significant reduction in the frequency of deep venous thrombosis (as diagnosed by contrast venography or ultrasonography) after hip and knee arthroplasty when mechanical or medical thromboprophylaxis is used. 7–11
It remains controversial whether the reduction in asymptomatic deep venous thrombosis results in a similar decrease in the frequency of clinically significant thromboembolic events such as fatal pulmonary embolism or postphlebitic syndrome. In a recent study, we demonstrated a consistent frequency of clinically relevant deep venous thrombosis (1.5%) and pulmonary embolism (0.7%) within 30 days of elective primary hip or knee arthroplasty over a 10-yr period that spanned the widespread adoption of routine thromboprophylactic strategies used in contemporary practice. 12
This article is featured in “This Month in Anesthesiology.” Please see this issue of Anesthesiology, page 5A.
Not all patients undergoing elective lower extremity joint replacement surgery are necessarily at the same risk for venous thromboembolism. Genetic influences may place specific patient populations at increased thromboembolic risk. 13
Other suggested risk factors for venous thromboembolic events in the general and surgical population include history of cigarette smoking, 14
hormone therapy, 16
and use of general instead of regional anesthetic techniques. 19
Additional risk factors for adverse thromboembolic events may be present after primary elective hip or knee arthroplasty, including surgeon-specific effects. 20
Optimization of perioperative treatment strategies may result in improved patient outcomes and decreased cost.
The purpose of this study was to evaluate the medical, surgical, and anesthetic risk factors potentially associated with increased frequency of clinically relevant thromboembolic complications in the perioperative period for patients undergoing lower extremity joint replacement. A case–control methodology is especially useful when the outcome/condition of interest (i.e.
, cases) occurs infrequently. 21
This methodology is well suited for the study of clinically significant thromboembolic events, because prospective ascertainment of surrogate markers may result in additional diagnosed events of undetermined clinical relevance. 21
In addition, the availability at our institution of a large and broadly based patient population allows retrospective examination of multiple potential risk factors. Therefore, we designed a case–control study of patients undergoing primary elective primary hip or knee arthroplasty who developed clinically relevant venous thromboembolism within 30 days of the surgical procedure.
Materials and Methods
This investigation includes patients who underwent primary elective total hip or knee arthroplasty at Mayo Clinic between January 1, 1986, and December 31, 1995. 12
All patients who underwent one or more elective primary total hip or knee replacements at our institution in the 10-yr study period were identified using prospectively collected databases, after review board approval. Patients who had denied research access to their medical records were excluded from the study (Minnesota state law [Minnesota Statute 144.335 Subd. 3a. (d)]). Our institutional total joint registry is a prospectively collected computerized database of all joint replacements performed at our institution since 1969 and has been validated previously. 22
Joint registry personnel abstract detailed information on surgical approach, prosthesis data operative indication, preoperative diagnoses, and postoperative medical and surgical complications and perform a formal chart review at 1, 2, and 5 yr and every 5 yr thereafter using a standardized data collection form. In a previous study, the overall rate of clinical follow-up within the total joint registry was greater than 95%. 22
The total joint registry was used to identify all patients who received one or more elective primary hip or knee joint replacements in the 10-yr study period. We excluded patients who received nonelective arthroplasty for fracture management. For patients who underwent more than one lower extremity arthroplasty during the study period, only the most recent procedure was considered. Thus, only one joint replacement episode was examined for each patient. All patients with evidence of a potential thromboembolic complication within the first year after the date of operation as documented in the total joint registry were identified, and their medical records were examined. As a cross-reference to the total joint registry, the institutional unified medical record system, which contains information on all patients who have ever been examined at Mayo Clinic, 23
was used to identify all patients treated with total hip or knee arthroplasty at our institution who had a diagnosis of pulmonary embolism or deep venous thrombosis at any time during the previous year, the year of, or the year after the surgical event. The medical records of all patients identified in either database search were retrospectively reviewed. Strict and validated criteria were used for the definition of adverse thromboembolic events. The level of diagnostic certainty was determined for each episode of pulmonary embolism or deep venous thrombosis occurring during the initial 30 days after the date of operation using previously defined criteria. 24
Patients meeting diagnostic criteria for probable events were not included as cases and were also excluded from the pool of potential controls. The patients meeting diagnostic criteria for definite thromboembolic events (table 1
) make up the cases for the current investigation.
For each case, we identified a pool of potential controls who had undergone the same surgery with the same surgeon. Using 1:1 matching of cases and controls, a control was selected as the individual with the closest surgery date before the surgery date for the case. The records of selected controls were reviewed to confirm the absence of noncoded thromboembolic events. Thus, each patient experiencing a definite adverse event was matched with a patient who underwent the same surgical procedure with the same surgeon, without an adverse event, and within a narrow time frame. All patient records were abstracted by a single investigator using standardized data collection forms. Demographic data and information on comorbid diseases, medications, and laboratory results were noted. Surgical procedure; anesthetic technique; and surgical, anesthetic, and recovery duration were recorded. Additional intraoperative and immediately postoperative information, including monitoring used and amount and type of fluids administered, was noted. Postoperative disposition, use of in-hospital thromboprophylaxis, postoperative analgesia, and duration of stay were also recorded.
Statistical analyses were performed using SAS® Software Release 6.12 (SAS Institute Inc., Cary, NC). Potential risk factors for perioperative thromboembolic events were assessed using conditional logistic regression, making use of the 1:1 matched-pair study design. Age, body mass index (weight in kilograms divided by the square of height in meters), hemoglobin concentration, duration of anesthesia, and duration of surgery were treated as continuous variables in the logistic regression analysis. The American Society of Anesthesiologists (ASA) physical status classification was adopted in 1962 for the grading of patients based on severity of illness and physiologic reserve. 25
For analysis purposes, ASA physical status was dichotomized (≤ 2 vs.
≥ 3). Other potential risk factors included in the logistic regression analysis were treated as categoric variables as presented in table 2
. Characteristics found to be statistically significant from the univariate analysis were included in a multivariate analysis with stepwise backward elimination of nonsignificant variables. To assess consistency in variable selection, a multivariate analysis was also performed using a stepwise forward procedure. To assess whether the effect of any potential risk factor changed over calendar time, two additional sets of analyses were performed. For each potential risk factor, an additional analysis was performed, which included the two-way interaction of the given risk factor with calendar time. In addition, because the use of routine thromboprophylactic strategies is known to have changed over the study period, the cases were separated into two groups, 1986–1990 (n = 66) and 1991–1995 (n = 50), to represent the periods before and after routine thromboprophylactic strategies were employed. Univariate analysis of risk factors was then performed separately for each group. In all cases, two-sided tests were used, with P
values ≤ 0.05 denoting statistical significance.
A total of 116 of 9,791 eligible patients undergoing elective primary hip or knee arthroplasty surgery in the 10-yr study period were found to have experienced one or more definite adverse thromboembolic events. The frequency of definite adverse thromboembolic events is displayed in figure 1
according to calendar time. There were 56 patients who experienced a definite pulmonary embolism and 68 patients who experienced a definite deep venous thrombosis, with 8 patients experiencing both events. There were an additional 34 patients who met criteria for a probable event but did not meet criteria for a definite event (24 for both pulmonary embolism and deep venous thrombosis, 10 for deep venous thrombosis only). These patients were not included as cases and were also not included in the pool of potential controls. Of the 116 cases, 39 patients underwent elective primary total hip arthroplasty, 49 underwent unilateral knee arthroplasty, and 28 underwent bilateral knee arthroplasty. Of the 68 patients who experienced deep venous thrombosis, 56 (82%) developed the thrombosis in an operative leg and 12 (18%) developed the thrombosis in a nonoperative leg. Overall, 43 patients (of the 116 cases [37%]) experienced the first venous thromboembolic event within 3 days after surgery, 43 (37%) from 4 to 10 days after surgery, and 30 (26%) from 11 to 30 days after surgery.
A summary of the univariate analysis of potential risk factors for thromboembolic events is presented in table 2
. The distribution of age and gender was similar for cases and controls. Treated as a continuous variable, larger body mass index was a significant risk factor for thromboembolic events (P
= 0.012; odds ratio [OR] = 1.5, 95% confidence interval (CI): 1.1–2.0 for each 5-kg/m2
increase). Obesity, defined as body mass index ≥ 30 kg/m2
, was observed in 56% of cases and 34% of controls (P
< 0.001; OR = 3.4, 95% CI: 1.7–6.6). A history of previous thromboembolic events was present for 9% of cases and 3% of controls (P
= 0.046; OR = 3.7, 95% CI: 1.0–13.1). The percentage of patients using antithrombotic agents (aspirin, warfarin, unfractionated heparin, or low-molecular-weight heparin preparations) on admission for lower extremity arthroplasty surgery was similar for cases (25%) and controls (24%), however. The percentages of patients classified as having ASA physical status 1, 2, 3, 4, and 5 were 3%, 39%, 55%, 3%, and 0% for cases and 0%, 63%, 35%, 2%, and 0% for controls, respectively. An ASA physical status classification of 3 or greater was significantly associated with an increased likelihood of a thromboembolic event (P
= 0.002; OR = 2.6, 95% CI: 1.4–4.7). Coronary artery disease, diabetes mellitus, and smoking status were not found to differ significantly between cases and controls.
Anesthetic technique (regional vs. general), duration of surgery, duration of anesthesia, transfusion of blood products, and use of postoperative neuraxial analgesia were similar in cases and controls and did not significantly alter the frequency of pulmonary embolism or deep venous thrombosis. The intraoperative use of invasive blood pressure monitoring via arterial cannulation was univariately associated with an increased risk for these adverse postoperative thromboembolic events (P = 0.028; OR = 2.8, 95% CI: 1.1–7.2), however. Other invasive intraoperative monitoring modalities, including central venous pressure and pulmonary artery catheters or transesophageal echocardiography, were used infrequently (<5% of cases) and not evaluated as potential risk factors. Postoperative intensive care unit admission was infrequent (2% of controls, 9% of cases) but was significantly associated with an increased likelihood of pulmonary embolism or deep venous thrombosis (P = 0.038; OR = 5.0, 95% CI: 1.1–22.8). All intensive care unit admissions in both groups were scheduled for patients thought to benefit from increased postoperative monitoring based on the preoperative medical assessment. No unplanned admissions based solely on intraoperative events were found in either group.
As expected, the use and choice of postoperative pharmacologic antithrombotic prophylaxis among cases and controls changed over calendar time (fig. 2
). The use of antithrombotic agents was found to be protective against the occurrence of clinically relevant thromboembolic events (P
= 0.038; OR = 0.2, 95% CI: 0.1–0.7 for aspirin or standard dose subcutaneous unfractionated heparin; OR = 0.5, 95% CI: 0.1–1.5 for warfarin or low-molecular-weight heparin). In patients who received aspirin or subcutaneous heparin thromboprophylaxis, the median time to initiation of treatment was the operative day in both cases and controls, and 89.0% of patients had it initiated by the first postoperative day. For patients receiving warfarin or low-molecular-weight heparin therapy, the median time to initiation was the operative day for both the cases and controls, and 99.3% of patients had it initiated by the first postoperative day.
From multivariate analysis after eliminating nonsignificant variables, body mass index (P = 0.031; OR = 1.5, 95% CI: 1.0–2.0 for each 5-kg/m2 increase), ASA physical status classification of 3 or greater (P = 0.005; OR = 2.6, 95% CI: 1.3–4.7), and use of antithrombotic prophylaxis (P = 0.050; OR = 0.2, 95% CI: 0.1–0.7 for aspirin or subcutaneous heparin; OR = 0.4, 95% CI: 0.1–1.4 for warfarin or low-molecular-weight heparin) were found to be independently associated with clinically relevant thromboembolic events. Using a stepwise forward selection procedure, the same set of independent predictors was identified. The effects of body mass index and ASA physical status classification ≥3 were found to change significantly over the 10-yr study period (P = 0.016 and P = 0.012 for the two-way interaction of calendar time with ASA physical status classification and body mass index, respectively). For each of these risk factors, the effect was significantly greater during the later years of the study. For body mass index, the OR increased from 1.1 (95% CI: 0.7–1.6) per 5-kg/m2 increase in the 1986–1990 period to 2.3 (95% CI: 1.4–3.9) per 5-kg/m2 increase in the 1991–1995 period. For ASA physical status classification ≥3, the OR increased from 1.5 (95% CI: 0.7–3.0) during the early period to 10.0 (95% CI: 2.3–42.8) during the 1991–1995 period. No other statistically significant risk factors were identified when analyses were performed separately for the 1986–1990 and 1991–1995 periods. Among cases, the duration of time from surgery to event diagnosis did not change significantly over calendar time (P = 0.171) and was not found to be associated with the use of pharmacologic antithrombotic prophylaxis (P = 0.172), ASA physical status classification (P = 0.877), or body mass index (P = 0.471).
Although the current study has limited statistical power to assess interaction effects, a question of specific interest is whether the use of regional versus general anesthesia reduces the risk of clinically relevant thromboembolic events in patients who do not receive pharmacologic antithrombotic prophylaxis. In the control group, regional anesthetic techniques were used in 6 of 8 (75%) patients not receiving prophylactic antithrombotic agents, in 13 of 39 (33%) patients receiving aspirin or subcutaneous heparin, and in 34 of 68 (50%) patients receiving warfarin or low-molecular-weight heparin. Among cases, regional anesthetic techniques were used in 8 of 19 (42%) patients not receiving prophylactic antithrombotic agents, in 9 of 27 (33%) patients receiving aspirin or subcutaneous heparin, and in 32 of 70 (46%) patients receiving warfarin or low-molecular-weight heparin. From an unmatched analysis of those who did not receive pharmacologic antithrombotic prophylaxis, the type of anesthetic technique was not found to differ significantly between cases and controls (use of regional technique in 8 of 19 patients vs. 6 of 8 patients for cases and controls, respectively; Fisher exact test, P = 0.21).
This study provides physicians involved in the perioperative care of arthroplasty patients information on the risk factors for clinically relevant perioperative thromboembolic morbidity after major elective orthopedic surgery of the lower extremities has been performed. An accurate assessment of the risks associated with these elective orthopedic surgeries should assist clinicians and their patients in decisions regarding treatment options and optimization of perioperative care. Anesthesiologists are increasingly involved in the preoperative preparation of their patients, improving both efficiency and cost-effectiveness. 26
The institution of therapeutic interventions geared toward improved perioperative outcomes might be critically dependent on the identification of patients at highest risk and timely initiation of appropriate therapies. Anesthesiologists might be best suited for this role.
The occurrence of pulmonary embolism and deep venous thrombosis within 30 days after elective primary total hip or knee arthroplasty was more frequent in patients with increasing body mass index, specifically those with a body mass index greater than 30 kg/m2, and in patients with moderate or severe systemic disease resulting in some functional limitation as defined by an ASA physical status classification greater than or equal to 3. For each of these risk factors, the effect was found to be significantly greater during the later years of the study, when pharmacologic antithrombotic prophylaxis with warfarin was common. In contrast, the use of pharmacologic antithrombotic prophylaxis after lower extremity orthopedic surgery was found to be protective. The choice of anesthetic technique, regional or general, did not measurably affect the risk of adverse thromboembolic events in this study. Although only in the univariate analysis, history of a previous venous thromboembolic event was associated with increased thromboembolic risk. Certainly, congenital and acquired thrombophilic disorders may contribute to venous thromboembolism. The interaction between hypercoagulable states and surgical procedures remains to be explored, however.
In several studies, 20,27,28
obesity was not found to be a risk factor for perioperative thromboembolic events in patients undergoing primary hip or knee replacement surgery. Benjamin et al.29
examined obesity as an independent risk factor for patients undergoing simultaneous bilateral knee replacement surgery in 455 patients but did not find significantly different rates of venous thromboembolism. Other studies, 17,18,30,31
including the present report, have found increased risk of pulmonary embolism or deep venous thrombosis in obese patients after lower extremity orthopedic surgery. In a survey of orthopedic surgeons, Rodgers et al.32
found that the majority of practitioners thought gross obesity was a risk factor for thromboembolic events. In fact, some authors have advocated the selective use of antithrombotic prophylaxis after total knee arthroplasty only in those patients with a history of previous deep venous thrombosis or obesity. 33
The present study specifically examined the risk of perioperative thromboembolic events in patients undergoing elective primary total hip or knee arthroplasty using a quantifiable grading of the extent of obesity. We also found that the association between obesity and perioperative thromboembolic events changed over time, with a larger effect observed during the later years of the study. Differences in the definition of obesity may underlie some of the reported differences in results. In addition, potential differences in patient populations (e.g.
, use of pharmacologic antithrombotic prophylaxis) may account for the disparity in results. Nevertheless, the conflicting results cannot be ascribed to differences in prospective ascertainment 18,27,30
or clinical diagnosis 17,20,28,29,34
In our study, the use of aspirin or subcutaneous heparin was as protective against the occurrence of clinically relevant pulmonary embolism or deep venous thrombosis within 30 days of elective primary total hip or knee replacement surgery as thromboprophylaxis with warfarin or low-molecular-weight heparin (OR = 0.2 and OR = 0.5, respectively). During the period of study, the First (1986) and Second (1988) American College of Chest Physicians Consensus Conferences recommended that patients undergoing elective knee arthroplasty surgery receive intermittent pneumatic compression, whereas those undergoing hip replacement receive either heparin or warfarin in doses sufficient to produce moderate anticoagulant effects. 35,36
Only the Fourth American College of Chest Physicians Consensus Conference (1995) included fixed-dose low-molecular-weight heparin as an alternative to any of these thromboprophylactic treatments. The incorporation of these recommendations into clinical practice at our institution is reflected by the increase in the use of pharmacologic thromboprophylaxis evident during the 10-yr study period (fig. 2
). The Sixth American College of Chest Physicians Consensus Conference on antithrombotic therapy evaluated available literature and reported results on specific strategies geared toward the prevention of venous thromboembolism in the general and surgical populations. 37
For instance, the use of mechanical and pharmacologic interventions was considered effective, and in specific high-risk groups, including the lower extremity orthopedic population, the use of pharmacologic antithrombotic therapy was highly recommended. Reductions of greater than 50% in the rate of asymptomatic prospectively ascertained pulmonary embolism and deep venous thrombosis are cited. 37
Despite the successful reduction of asymptomatic thromboembolic disease with the use of routine anticoagulation, an actual reduction of clinically relevant adverse events has been difficult to demonstrate in everyday medical practice. 38
Although there is a large amount of clinical data documenting the efficacy and cost-effectiveness of routine thromboprophylaxis in patients undergoing elective total hip or knee replacement surgery, 37
it is likely that selected patient populations might receive the most benefit from specific prophylactic measures. 12,38
A targeted selective approach to perioperative thromboprophylaxis may reduce the incidence of hemorrhagic complications 39
resulting from unnecessary therapy in patients at low risk of thromboembolic complications while appropriately treating those patients at higher risk. In addition, the delayed occurrence of a number of thromboembolic events (28% of cases occurred more than 10 days after surgery) would suggest that additional antithrombotic prophylaxis beyond the duration of hospitalization might be warranted in certain patient populations. These hypotheses remain to be tested.
Multiple studies have found a surgery-specific association between ASA physical status classification and perioperative morbidity and mortality. 40–42
The ASA physical status classification subjectively stratifies patients independent of the surgical procedure planned according to their severity of illness, which, in turn, may determine the occurrence of adverse outcomes. In our study, patients undergoing primary elective lower extremity arthroplasty surgery with an ASA physical status classification of 3 or greater were found to be at increased risk of clinically relevant deep venous thrombosis or pulmonary embolism within 30 days. Similarly, intraoperative placement of an arterial line for continuous arterial blood pressure monitoring and/or repeated sampling and planned postoperative intensive care unit admission were predictive of an increased risk of thromboembolic events within 30 days of elective primary hip or knee arthroplasty surgery. It is likely that these findings represent surrogate markers for other variables, including patient sickness profile. Accordingly, increasing age has been associated with increased thromboembolic risk in the orthopedic population. 12,31
In the present study, we did not observe a measurably increased frequency of deep venous thrombosis or pulmonary embolism in older patients. It is possible that differences in overall well-being (i.e.
, sickness profile) rather than age determine the perioperative risk of thromboembolic complications.
Earlier studies had suggested that the use of regional anesthetic techniques such as the subarachnoid or epidural administration of local anesthetics for the administration of surgical levels of anesthesia was associated with reduced risk of perioperative thromboembolic events in the lower extremity arthroplasty population. 19,43
In the present study, we did not observe a measurable effect of anesthetic technique on the risk of deep venous thrombosis or pulmonary embolism in patients treated with elective lower extremity arthroplasty. Differences in patient selection or use of adjuvant measures, including early ambulation or pneumatic compression, may have been responsible for the reported protective effect. By matching on surgeon and type of surgery, we have likely accounted for these differences in patient management and thus are better able to define the specific role of regional anesthesia (including postoperative neuraxial analgesia) in the prophylaxis against deep venous thrombosis or pulmonary embolism after lower extremity arthroplasty.
There are limitations inherent to the design of this study. As with all case–control studies, our findings only provide information on relative risk rather than on absolute risk; this limits the applicability to clinical practice. Similarly, the quality of the data is dependent on the accuracy and completeness of the medical record. Our investigation was restricted to data routinely collected as part of the medical record or the total joint registry. In addition, a single investigator abstracted all the data using standardized data collection forms. It is possible that a previous thromboembolic event or other variable may have led to specific changes in the management of the patient(s). In the present study, there were no differences in the history of thromboembolism between the cases and controls.
The effective sample size for assessing a given risk factor in a matched case–control study is determined by the number of discordant matched pairs (i.e., the number of matched pairs in which the value of the given risk factor differs for case and control). For this investigation, matching on surgeon, surgical procedure, and calendar time resulted in a small effective sample size for assessing some risk factors such as type of antithrombotic prophylaxis used. We also have limited power to assess interaction effects such as whether regional anesthesia is protective in the absence of anticoagulant use. Among those who did not receive pharmacologic antithrombotic prophylaxis, the use of regional anesthetic techniques did not differ significantly between cases and controls. Given the small sample size, however, this observation should be not be interpreted as evidence of no association.
In the present study, although nonpharmacologic antithrombotic measures were not routinely used at our institution, it is possible that some patients might have received intermittent pneumatic compression devices during their hospital course. Documentation of their use was not performed in a standardized fashion, however, and thus was not available for review. Although several small studies have shown that intermittent pneumatic compression is an effective form of prophylaxis (specifically after total knee replacement surgery), its effectiveness depends on continuous wear immediately after surgery (both in the hospital and after discharge). Thus, current recommendations indicate that these devices are most useful when used concurrently with pharmacologic antithrombotic regimens. Nonetheless, a significant protective effect of the use of some form of thromboprophylaxis is evident in the present study. Other studies have demonstrated similar reductions in the rates of clinically relevant thromboembolic events in patients receiving aspirin, warfarin, or low-molecular-weight heparin. 44,45
The results of the present study are consistent with a significant reduction in the rate of clinically relevant adverse thromboembolic events with the use of aspirin. The Pulmonary Embolism Prevention Trial Collaborative Group examined the frequency of symptomatic deep venous thrombosis and pulmonary embolism in patients receiving elective hip or knee arthroplasty or after hip fracture and reported reductions in these adverse outcomes with the use of aspirin (when compared with placebo) 45
similar to those reported for prophylactic warfarin or low-molecular-weight heparin. 44
The actual impact on disease prevention of routine warfarin and low-molecular-weight heparin thromboprophylaxis in the orthopedic population needs further study. In fact, the clinical relevance of venographically or ultrasonographically ascertained lower extremity thrombi after hip or knee arthroplasty surgery remains to be determined, because most of these thrombi resolve without coming to clinical attention. 44
In the present study, the effects of body mass index and ASA physical status classification ≥3 were greater during the time when the thromboprophylactic use of warfarin or low-molecular-weight heparin became routine. The prevention of clinically relevant venous thromboembolic events after lower extremity arthroplasty might need optimization, because not all patients receiving pharmacologic thromboprophylaxis are at equal risk. For instance, a weight-based and/or sickness-adjusted thromboprophylactic regimen may further reduce thromboembolic risk while avoiding unnecessary treatment of low-risk patients. These hypotheses remain to be explored.
In conclusion, this study demonstrates the existence of specific risk factors within the general orthopedic population for the occurrence of adverse perioperative thromboembolic events in patients undergoing elective lower extremity joint replacement surgery managed with current operative and perioperative care. The routine use of antithrombotic prophylaxis might require optimization in specific patient populations, as suggested by the findings of increased risk in obese patients, defined by a body mass index greater than 30 kg/m2, and in patients with higher sickness profiles, as determined by an ASA physical status classification of 3 or greater.
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