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Nelson, Shaffrey, Satalich, Hopper, O’Neill, Edge, Ernst, and Vanderbeck: Acute complications after reverse total shoulder arthroplasty for treatment of cuff arthropathy versus fracture

Abstract

Background

Reverse total shoulder arthroplasty (RTSA) has become increasingly popular in recent years, and this trend is expected to continue. However, differences in outcomes of RTSA for fractures compared with other indications are poorly understood. This study aimed to identify the compare the incidences of adverse events during RTSA to treat cuff tear arthropathy (CTA) versus RTSA to treat fractures, as well as identify risk factors for any adverse event.

Methods

Patients who underwent RTSA from 2010 to 2020 in the National Surgical Quality Improvement Program database were included. Matched cohorts were created using nearest-neighbor matching. Independent sample t-tests and chi-square tests were used to determine differences between groups, and binary logistic regression was performed to determine odds ratios and 95% CIs.

Results

In total, 27,607 CTA patients (94.5%) and 1,537 fracture patients (5.3%) underwent RTSA. Adverse events occurred in 1,088 CTA patients (3.9%) and 192 fracture patients (12.4%). Incidences of adverse events, postoperative transfusions, and returns to an operating room were all significantly higher in the fracture cohort compared with CTA patients.

Conclusions

Following surgery, higher rates of adverse events were observed in the CTA patients compared with those in the fracture cohort. These findings improve our understanding of the effectiveness of an increasingly popular surgical intervention due to the use of a large database analysis to identify short-term complications and risk factors.

Level of evidence

III.

INTRODUCTION

Reverse total shoulder arthroplasty (RTSA) has become an increasingly popular and useful procedure in recent decades [1]. Although originally designed for treatment of cuff tear arthropathy (CTA), improvements in implant design [2], surgeon technique, and surgeon experience have expanded the indications for RTSA to a breadth of shoulder pathologies [3]. RTSA offers improved range of motion, joint and muscle loading, and overall joint stability, making it an attractive intervention for complex shoulder disorders, including massive rotator cuff tear (MCT) with or without glenohumeral osteoarthritis, primary osteoarthritis, failed primary shoulder arthroplasty, and proximal humeral fracture (PHF) [4-6].
Considerable research has been conducted, with positive outcomes reported following RTSA across various preoperative diagnoses, including CTA, MCT, and PHF. A comparison of results following RTSA versus shoulder hemiarthroplasty for PHF has been associated with “more favorable clinical outcomes” in terms of functional scores, pain relief, and revision rates for patients treated with RTSA [7]. As a result, RTSA has become a leading treatment option for PHF, with utilization rates increasing by 400% between 2005 and 2012 [3,8]. Despite this growing popularity, few attempts have been made to assess the differences in outcomes of RTSA for PHF compared with other preoperative diagnosis.
While the RTSA may yield improved outcomes for pain and function when treating PHF, this preoperative diagnosis may elicit surgical challenges and postoperative complications compared to that of RTSA for CTA [9]. Patients with PHF typically present with unique demographics, preoperative comorbidities, and functional demands that may influence surgical outcomes following RTSA [10]. The primary aim of this study was to determine if there was a difference in the incidence of adverse events (AEs) in RTSA to treat CTA versus a fracture. Second, this study aimed to identify patient risk factors for any AE among and between patients who underwent RTSA for CTA versus fracture.

METHODS

Patient Population

This was a retrospective comparative analysis of data from the National Surgical Quality Improvement Program (NSQIP), which is managed by the American College of Surgeons. NSQIP data were collected by a certified surgical clinical reviewer at each participating site. Participant use data files (PUFs) from 2010 to 2020 were used in this analysis, including those for patients who underwent surgery from January 2010 to December 2020. The NSQIP uses a systematic sampling process to determine which cases are included in the PUF. All patients were followed for 30 days postoperative.
The inclusion criteria for this analysis were any patients who underwent RTSA to treat CTA or fracture. NSQIP criteria for case exclusion included minors (younger than 18 years; cases secondary to urgent, high-acuity situations such polytraumas that may confound quality assessment; and patients who returned to the operating room due to a complication from a prior procedure. The data for this analysis were cleaned in R Studio version 2023.06.0 (R Foundation for Statistical Computing) to exclude patients who had an operation time or body mass index (BMI) less than or equal to 0 minutes (R studio). Cases were also excluded if functional status, dyspnea status, sex, or American Society of Anesthesiologists (ASA) class were not supplied. If the principal anesthesia technique was “none,” “not reported,” or “other,” the case was excluded.

Variables

The independent variable for this analysis was indication for RTSA (CTA or fracture). The dependent variables were AEs following surgery. The outcomes of interest were death, wound dehiscence, sepsis, pulmonary embolism, renal complication, myocardial infarction, cardiac arrest, stroke, transfusion, deep vein thrombosis, urinary tract infection, pneumonia, intubation issues, surgical site infection, and return to the operating room. AEs included all of these complications.

Intervention

Current procedural terminal code 23472 was used to define patients that underwent RTSA. International Classification of Diseases, Tenth Revision (ICD-10) codes were used to define patients who underwent reverse TSA to treat CTA or fracture (Table 1). All patients were followed for at least 30 days following surgery.

Statistical Plan

Matched cohorts were created using the nearest neighbor method to match patients according to age, BMI, sex, race, diabetes, smoking status, ASA class, hypertension requiring medication, congestive heart failure, chronic obstructive pulmonary disease (COPD), and bleeding disorders. IBM SPSS version 28.0.1.1 (IBM Corp.) was used for statistical analyses. Independent sample t-tests were used to determine if there was a difference between the CTA and fracture groups for continuous variables. Fisher’s exact tests were used where possible to determine if there was a difference between indications for surgery for categorical variables. If a Fisher’s exact test was unable to be performed, a chi-square test was used. Binary logistic regression was performed to determine the odds ratios (ORs) and 95% CIs with any AE as the dependent variable and patient demographics and comorbidities as covariates for the combined matched group. Results were statistically significant at a P-value ≤0.05.

RESULTS

Demographics

Between the years 2010 to 2020, a total of 27,607 patients (94.5%) in the study group underwent RTSA for CTA and 1537 patients (5.3%) underwent RTSA for fracture. Patients who underwent RTSA for CTA had a mean age of 69.0±9.3 years and a mean BMI of 31.2±6.8 kg/m2, and 45.7% were male. Patients receiving RTSA for fracture had a mean age of 72.0±9.1 years and a mean BMI of 30.3±7.4 kg/m2, and 18.4% were male. Current smokers accounted for 10.2% of CTA patients and 12.4% of fracture patients. The most common preoperative comorbidities were non-insulin–dependent diabetes (12.6% and 14.2%) and COPD (6.6% and 7.2%) for both the CTA and fracture patients, respectively. Full demographic information is summarized in Table 2.

Incidence of AEs

AEs within the 30-day postoperative period occurred in 1,088 CTA patients (3.9%) and 192 fracture patients (12.4%). However, after matching by near-equal patient characteristics among the two cohorts, CTA patients had a higher rate of AEs (4.6%) compared with fracture patients (12.4%). Postoperative transfusion (1.6% and 8.7%, respectively) was the most common AE in both cohorts of patients. A return to the operating room was necessary in 1.3% of CTA patients and 3.1% of fracture patients. Incidences of AEs, postoperative transfusions, and returns to the operating room were all significantly higher among fracture patients compared with CTA patients (all P<0.001) (Table 3).

Risk Factors for Any AEs

Following RTSA for CTA, increasing age (OR=1.022, P<0.001), BMI (OR=0.988, P=0.015), insulin-dependent diabetes mellitus (OR=1.447, P=0.004), congestive heart failure (OR=1.773, P=0.025), preoperative transfusion (OR=3.069, P=0.006), history of bleeding disorder (OR=1.945, P<0.001), operative time (OR=1.006, P<0.001), length of stay (OR=1.081, P<0.001), functional status (OR=6.212, P<0.001), COPD (OR=1.284, P=0.022), and history of MI (OR=1.394, P<0.001) were all significant risk factors for any AE, while male sex (OR=0.726, P<0.001) was a protective factor.
For patients who underwent RTSA for fracture, age (OR=1.030, P=0.010), preoperative transfusion (OR=3.179, P=0.015), bleeding disorder (OR=2.367, P=0.004), operative time (OR=1.009, P<0.001), length of stay (OR=1.106, P<0.001), and renal failure (OR=12.094, P=0.040) were all significant risk factors for any AE (Table 4).

DISCUSSION

This study aimed to identify any difference between the incidence of AEs (within a 30-day follow-up window) in patients receiving RTSA to treat CTA and those receiving RTSA to treat fractures. After matching, the overall rates of AEs, operative time, length of stay, postoperative transfusions, and return to operating room were significantly higher in patients undergoing RTSA for fractures, with secondary findings that include identification of independent risk factors for any AE for each cohort. A discussion of these results in the context of the literature and relevant surgical considerations is warranted.
Compared with the CTA cohort, the demographics of the patients undergoing RTSA for traumatic fractures, prior to matching, showed dramatically greater rates of female sex, greater average age, higher ASA classifications, dependent functional status, and multiple comorbidities (Table 2). Taken together, these results suggest that RTSA for trauma selects a patient population with lower levels of baseline health at the time of operation. Likewise, compared with the RTSA for CTA cohort, these trauma patients are often limited by time and circumstances that prevent risk-factor modification and preoperative intervention, given the sudden injury and relative immediacy of surgery.
Other baseline differences may be poorer bone quality in the trauma group compared with the CTA group, as evidenced by risk factors such as advanced age and greater percentage of female sex [8]. This association is also supported by the profile of PHF patients treated by RTSA as established in the literature: low-demand, elderly patients with poor bone stock, fracture dislocation, non-constructible tuberosities, or failed conservative management [8]. However, despite age being a known risk factor, a recent study by Stenquist et al. [11] reported no differences in functional outcomes in two cohorts divided by age (mean age, 64 vs. 78 years) post-RTSA for complex PHF with a 3-year minimum follow-up period. As such, future studies are needed to clarify these trends, associations, and long-term outcomes between baseline health, poor bone quality, and implant survival in RTSA for traumatic fractures [12,13].
Regarding rates of AEs in this trauma cohort, this analysis identified risk factors including age, preoperative transfusion, and bleeding disorders, among others (Table 4). Among the many possible factors contributing to these findings, one consideration is the association of advanced age with higher rates of coagulopathies, blood thinners, and traumatic falls [14]. Taken together, these findings suggest that a greater degree of bleeding from soft tissues at the fracture sight and around the time of surgery necessitates transfusions or creates technical difficulties in surgery to navigate intraoperative bleeding or hematomas. These factors could contribute to the increased operative times and rates of return to operating rooms seen in the trauma cohort.
As the unpredictability of acute injuries such as PHF creates an inability to modify certain risk factors, future studies targeting ideal surgical time parameters and patient comorbidity characteristics would be useful. Surgeons would be wise to continue using their best judgment when considering surgical delays for medical optimization efforts in the setting of painful and morbid fractures for patients. Regarding rates of AEs in the CTA cohort, independent risk factors included age, BMI, insulin-dependent diabetes mellitus, CHF, COPD, history of bleeding disorder, increased operating time, length of stay, functional status, and history of myocardial infarction. Notably, male sex was a protective factor for AEs in this cohort. Given that RTSA for arthropathy is typically an elective surgery, there is time for risk-factor modification and medical optimization; a recent study by Churchill et al. [15] outlined guidelines for such an approach in RTSA patients. Surgeons can use these data in conjunction with the existing literature to educate patients and make preoperative plans in pursuit of optimal outcomes and mitigated risks.
This study is limited due to its retrospective design and lack of causative insight. Further inherent limitations of retrospective database studies include selection bias, lack of surgical details, and human error in the NSQIP data-collection methodology [16]. This study cannot control confounding factors such as surgeon experience, skill, and technique [14,17,18]. This study only reports complications in the database within a 30-day follow-up. As such, it does not report on important surgical complications unique to RTSA surgery, such as instability/dislocation, acromial stress fracture, posttraumatic osteoarthritis, hardware failure, and implant loosening, which are either not in the NSQIP or take place over much longer periods of time [19,20]. Other indications for RTSA were not evaluated or compared outside of the arthropathies and fractures classified as we were limited by procedure and indication coding.

CONCLUSIONS

This study used the NSQIP database to compare short-term complications in patients undergoing RTSA for acute traumatic fractures versus chronic CTA indications. Prior to matching, the trauma cohort had higher rates of female patients, older ages, higher ASA scores, greater functional dependency, and higher rates of multiple comorbidities. RTSA for trauma was also associated with longer operative times and hospital stays, higher transfusion rates, and more frequent returns to the operating room. While limited by its retrospective, database-based design and lack of long-term orthopedic outcomes, the findings of this study should help inform surgeons and patients about the short-term risks associated with RTSA for trauma.

NOTES

Author contributions

Conceptualization: JS, CON, CE, BE, JLV. Data curation: CTN, IS, HH. Formal analysis: CTN, IS, HH, Investigation: CTN, JS, HH, CON, CE, BE, JLV. Methodology: CTN, HH, CON. Project administration: JLV. Software: HH. Supervision: JS, CON, CE, BE, JLV. Validation: JS, CON, CE, BE. Visualization: CTN, IS. Writing – original draft: CTN, IS. Writing – review & editing: CTN, IS, JS, HH, CON, CE, BE, JLV. All authors read and agreed to the published version of the manuscript.

Conflict of interest

None.

Funding

None.

Data availability

Contact the corresponding author for data availability.

Acknowledgments

None.

Table 1.
International Classification of Diseases, Tenth Revision (ICD-10) codes
Group ICD-10 code Description
Arthropathy M19.011 Primary osteoarthritis, right shoulder
M19.012 Primary osteoarthritis, left shoulder
M75.101 Unspecified rotator cuff tear or rupture of right shoulder, not specified as traumatic
M12.811 Other specific arthropathies, not elsewhere classified, right shoulder
M75.102 Unspecified rotator cuff tear or rupture of left shoulder, not specified as traumatic
M75.121 Complete rotator cuff tear or rupture of right shoulder, not specified as traumatic
M12.812 Other specific arthropathies, not elsewhere classified, left shoulder
M19.01 Primary osteoarthritis, shoulder
M75.122 Complete rotator cuff tear or rupture of left shoulder, not specified as traumatic
M12.9 Arthropathy, unspecified
M19.111 Post-traumatic osteoarthritis, right shoulder
M19.019 Primary osteoarthritis, unspecified shoulder
M19.112 Post-traumatic osteoarthritis, left shoulder
M13.811 Other specified arthritis, right shoulder
M19.211 Secondary osteoarthritis, right shoulder
M19.90 Unspecified osteoarthritis, unspecified site
M12.511 Traumatic arthropathy, right shoulder
M75.1 Rotator cuff tear or rupture, not specified as traumatic
M13.812 Other specified arthritis, left shoulder
M12.512 Traumatic arthropathy, left shoulder
M19.212 Secondary osteoarthritis, left shoulder
S46.011A Strain of muscle(s) and tendon(s) of the rotator cuff of right shoulder, initial encounter
S46.012A Strain of muscle(s) and tendon(s) of the rotator cuff of left shoulder, initial encounter
M75.111 Incomplete rotator cuff tear or rupture of right shoulder, not specified as traumatic
M19.11 Post-traumatic osteoarthritis, shoulder
Incomplete rotator cuff tear or rupture of left shoulder, not specified as traumatic
M75.100 Unspecified rotator cuff tear or rupture of unspecified shoulder, not specified as traumatic
M12.819 Other specific arthropathies, not elsewhere classified, unspecified shoulder
M06.9 Rheumatoid arthritis, unspecified
M06.811 Other specified rheumatoid arthritis, right shoulder
M19.0 Primary osteoarthritis of other joints
M75.120 Complete rotator cuff tear or rupture of unspecified shoulder, not specified as traumatic
Fracture S42.201A Unspecified fracture of upper end of right humerus, initial encounter for closed fracture
S42.202A Unspecified fracture of upper end of left humerus, initial encounter for closed fracture
S42.291A Other displaced fracture of upper end of right humerus, initial encounter for closed fracture
S42.292A Other displaced fracture of upper end of left humerus, initial encounter for closed fracture
S42.241A 4-Part fracture of surgical neck of right humerus, initial encounter for closed fracture
S42.242A 4-Part fracture of surgical neck of left humerus, initial encounter for closed fracture
S42.202K Unspecified fracture of upper end of left humerus, subsequent encounter for fracture with nonunion
S42.251A Displaced fracture of greater tuberosity of right humerus, initial encounter for closed fracture
S42.211A Unspecified displaced fracture of surgical neck of right humerus, initial encounter for closed fracture
S42.201P Unspecified fracture of upper end of right humerus, subsequent encounter for fracture with malunion
S42.201K Unspecified fracture of upper end of right humerus, subsequent encounter for fracture with nonunion
S42.252A Displaced fracture of greater tuberosity of left humerus, initial encounter for closed fracture
S42.212A Displaced fracture of greater tuberosity of left humerus, initial encounter for closed fracture
S42.232A 3-Part fracture of surgical neck of left humerus, initial encounter for closed fracture
S42.202P Unspecified fracture of upper end of left humerus, subsequent encounter for fracture with malunion
S42.231A 3-Part fracture of surgical neck of right humerus, initial encounter for closed fracture
S42.351A Displaced comminuted fracture of shaft of humerus, right arm, initial encounter for closed fracture
S42.91XA Fracture of right shoulder girdle, part unspecified, initial encounter for closed fracture
Table 2.
Demographic and comorbidity characteristics of patients undergoing RTSA for CTA or fracture
Variable Arthropathy Fracture P-value Arthropathy matched Fracture matched P-value
No. of patients 27,607 (94.7) 1,537 (5.3) - 1,537 (50.0) 1,537 (50.0) -
Age (yr) 69.0±9.3 72.0±9.1 <0.001 71.9±9.2 72.0±9.1 0.852
BMI (kg/m2) 31.2±6.8 30.3±7.4 <0.001 29.9±6.6 30.3±7.4 0.146
Male sex 12,619 (45.7) 283 (18.4) <0.001 287 (18.7) 283 (18.4) 0.853
Operative time (min) 107.9±44.3 125.0±47.7 <0.001 105.2±43.5 125.0±47.7 <0.001
Length of stay (day) 1.6±3.3 2.6±4.7 <0.001 1.6±4.9 2.6±4.7 <0.001
Outpatient status 2,986 (10.8) 193 (12.6) 0.034 145 (9.4) 193 (12.6) 0.007
ASA class <0.001 0.502
 1 (No disturbance) 423 (1.5) 14 (0.9) 12 (0.8) 14 (0.9)
 2 (Mild disturbance) 11,497 (41.6) 505 (32.9) 529 (34.4) 505 (32.9)
 3 (Severe disturbance) 14,899 (54.0) 910 (59.2) 906 (58.9) 910 (59.2)
 4 (Life-threatening disturbance) 784 (2.8) 108 (7.0) 90 (5.9) 108 (7.0)
 5 (Moribund) 4 (0.0) 0 0 0
Race <0.001 0.948
 White 22,978 (83.2) 1,355 (88.2) 1,346 (87.6) 1,355 (88.2)
 Black 1,347 (4.9) 37 (2.4) 34 (2.2) 37 (2.4)
 Other 356 (1.3) 30 (1.9) 34 (2.2) 30 (1.9)
 Unknown 2,926 (10.6) 115 (7.5) 123 (8.0) 115 (7.5)
Dependent functional status (partial or total) 576 (2.1) 76 (4.9) <0.001 52 (3.4) 76 (4.9) 0.018
Current smoker 2,829 (10.2) 194 (12.6) 0.004 205 (13.3) 194 (12.6) 0.556
Comorbidity
 CHF 166 (0.6) 26 (1.7) <0.001 23 (1.5) 26 (1.7) 0.774
 Renal failurea) 11 (0.0) 4 (0.3) 0.007 0 4 (0.3) 0.125
 Dialysisb) 89 (0.3) 10 (0.7) 0.041 6 (0.4) 10 (0.7) 0.453
 Steroid use 1,343 (4.9) 64 (4.2) 0.246 74 (4.8) 64 (4.2) 0.433
 Malnourishment 57 (0.2) 10 (0.7) 0.003 2 (0.1) 10 (0.7) 0.038
 Bleeding disorder 668 (2.4) 80 (5.2) <0.001 64 (4.2) 80 (5.2) 0.200
 Ascites 3 (0.0) 2 (0.1) 0.025 1 (0.1) 2 (0.1) 1.000
 Preoperative transfusion 42 (0.2) 28 (1.8) <0.001 2 (0.1) 28 (1.8) <0.001
 Diabetes <0.001 0.623
  IDDM 1,361 (4.9) 159 (10.3) 165 (10.7) 159 (10.3)
  NIDDM 3,487 (12.6) 218 (14.2) 200 (13.0) 218 (14.2)
 DOE 1,865 (6.8) 99 (6.4) 0.003 115 (7.5) 99 (6.4) 0.221
 COPD 1,824 (6.6) 110 (7.2) 0.401 115 (7.5) 110 (7.2) 0.782

Values are presented as number (%) or mean±standard deviation.

RTSA: reverse total shoulder arthroplasty, CTA: cuff tear arthropathy, BMI: body mass index, ASA: American Society of Anesthesiologists, CHF: congestive heart failure, IDDM: insulin-dependent diabetes mellitus, NIDDM: non-insulin dependent diabetes, DOE: dyspnea on exertion, COPD: chronic obstructive pulmonary disease.

a)Renal failure: wherein renal function has been compromised within 24 hours prior to surgery;

b)Dialysis: acute or chronic renal failure requiring dialysis within 2 weeks of indexed procedure.

Table 3.
Incidence of adverse events for patients undergoing RTSA for CTA or fracture
Variable Arthropathy unmatched
Fracture unmatched
P-value Arthropathy matched
Fracture matched
P-value Overall
No. Rate (%) No. Rate (%) No. Rate (%) No. Rate (%) No. Rate (%)
Any adverse eventa) 1,088 3.9 192 12.4 <0.001 71 4.6 192 12.4 <0.001 263 8.6
 Death 42 0.2 12 0.8 <0.001 4 0.3 12 0.8 0.076 16 0.5
 Wound dehiscence 17 0.1 1 0.1 1.000 2 0.1 1 0.1 1.000 3 0.1
 Sepsis 48 0.2 8 0.5 0.009 4 0.3 8 0.5 0.387 12 0.4
 Pulmonary embolism 78 0.3 6 0.4 0.707 5 0.3 6 0.4 1.000 11 0.4
 Renal complicationb) 39 0.1 2 0.1 1.000 3 0.2 2 0.1 1.000 5 0.2
 MI 64 0.2 11 0.7 0.001 4 0.2 11 0.7 0.118 15 0.5
 Cardiac arrest 15 0.1 2 0.1 0.225 0 0.0 2 0.1 0.500 2 0.1
 Stroke 24 0.1 1 0.1 1.000 1 0.1 1 0.1 1.000 2 0.1
 Transfusion 439 1.6 134 8.7 <0.001 40 2.6 134 8.7 <0.001 174 5.7
 DVT 144 0.5 19 1.2 0.001 7 0.5 19 1.2 0.019 26 0.8
 UTI 180 0.7 23 1.5 <0.001 12 0.8 23 1.5 0.088 35 1.1
 Pneumonia 124 0.4 16 1.0 0.003 5 0.3 16 1.0 0.017 21 0.7
 Intubation issuesc) 55 0.2 8 0.5 0.017 4 0.3 8 0.5 0.387 12 0.4
 SSI 143 0.5 11 0.7 0.277 4 0.3 11 0.7 0.118 15 0.5
Return to operating room 356 1.3 48 3.1 <0.001 20 1.3 48 3.1 <0.001 68 2.2

RTSA: reverse total shoulder arthroplasty, CTA: cuff tear arthropathy, MI: myocardial infarction, DVT: deep vein thrombosis, UTI: urinary tract infection, SSI: surgical site infection.

a)Any adverse event: superficial and deep surgical site infection, organ space infection, renal failure or insufficiency, intubation (fail to wean or reintubation), postoperative transfusion, pneumonia, DVT, pulmonary embolism, UTI, stroke, cardiac arrest, MI, return to operating room;

b)Renal complication: progressive renal insufficiency or renal failure;

c)Intubation issues: reintubation or failure to wean from intubation.

Table 4.
Odds of developing any adverse event during surgery as related to patient demographics and comorbidities
Variable Arthropathy
Fracture
Combined matched
Odds ratio (95% CI) P-value Odds ratio (95% CI) P-value Odds ratio (95% CI) P-value
Procedure (fracture) - - - - 2.175 (1.590–2.975) <0.001
Age 1.022 (1.014–1.030) <0.001 1.030 (1.007–1.054) 0.010 1.021 (1.002–1.040) 0.026
BMI 0.988 (0.979–0.998) 0.015 - - 0.971 (0.950–0.993) 0.009
Sex (male less risk) 0.726 (0.636–0.828) <0.001 - - - -
ASA class - <0.001 0.001 - 0.002
IDDM 1.417 (1.119–1.795) 0.004 - - - -
Congestive heart failure 1.773 (1.075–2.922) 0.025 - - - -
Preoperative transfusion 3.069 (1.388–6.787) 0.006 3.179 (1.253–8.067) 0.015 3.228 (1.340–7.773) 0.009
Bleeding disorder 1.945 (1.470–2.573) <0.001 2.367 (1.327–4.220) 0.004 2.036 (1.253–3.307) 0.004
Operative time 1.006 (1.005–1.007) <0.001 1.009 (1.005–1.012) <0.001 1.008 (1.005–1.011) <0.001
Length of stay 1.081 (1.064–1.099) <0.001 1.106 (1.053–1.162) <0.001 1.125 (1.080–1.172) <0.001
Functional status (totally dependent compared to independent) 6.212 (2.402–16.063) <0.001 - - 1.756 (1.015–3.307) 0.044
Renal failure - - 12.094 (1.125–130.073) 0.040 12.998 (1.249–135.265) 0.032
COPD 1.284 (1.036–1.592) 0.022 - - - -
MI 1.394 (1.149–1.691) <0.001 - - - -

BMI: body mass index, ASA: American Society of Anesthesiologists, IDDM: insulin-dependent diabetes mellitus, COPD: chronic obstructive pulmonary disease, MI: myocardial infarction.

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