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Arthroplasty Today Cementation of a monoblock dual mobility bearing in a newly-implanted porous revision acetabular component in patients undergoing revision total hip arthroplasty --Manuscript Draft-- Manuscript Number: ARTD-D-19-00024R2 Article Type: Original Research Keywords: Revision hip arthroplasty; dislocation; instability; cemented dual mobility; fully porous shell Corresponding Author: Ran Schwarzkopf, MD, MSc NYU Hospital for Joint Diseases, NYU Langone Medical Center New Rochelle, NY United States First Author: Jonathan A Gabor, BS Order of Authors: Jonathan A Gabor, BS James E Feng, MD Shashank Gupta, BE Tyler E Calkins, BS Craig J Della Valle, MD Jonathan Vigdorchik, MD Ran Schwarzkopf, MD MSc Abstract: Background: The most common indications for revision total hip arthroplasty (rTHA) are instability/dislocation and mechanical loosening. Efforts to address this have included the use of dual mobility (DM) articulations. The aim of this study is to report on the use of cemented DM cups in complex acetabular rTHA cases with a high risk of recurrent instability. Methods: A multicenter, retrospective study was conducted. Patients who received a novel acetabular construct consisting of a monoblock DM cup cemented into a fully porous metal shell were included. Outcomes data included 90-day complications and readmissions, revision for any reason, and Harris Hip Scores. Results: Thirty-eight hips in 38 patients were included for this study. At a median follow-up of 215.5 days (range, 6–783 days), the Harris Hip Score improved from a mean of 50 ± 12.2 to 78 ± 11.2 (p<0.001). One (2.6%) patient experienced a dislocation on postoperative day 1, and was closed reduced with no further complications. There was one (2.6%) reoperation for periprosthetic joint infection treated with a two-stage exchange. Conclusions: In this complex series of patients, cementation of a monoblock DM cup into a newly-implanted fully porous revision shell reliably provided solid fixation with a low risk of dislocation at short-term follow-up. While longer term follow-up is needed, utilization of this novel construct should be considered in patients at high risk for instability. Powered by Editorial Manager® and ProduXion Manager® from Aries Systems Corporation
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Page 1: Arthroplasty Today · Shashank Gupta, BE1 Tyler E. Calkins, BS2 Craig J. Della Valle, MD2 Jonathan Vigdorchik, MD3 Ran Schwarzkopf MD MSc1 Author Affiliations: 1D epa rtm n of OrthopedicSurg

Arthroplasty Today

Cementation of a monoblock dual mobility bearing in a newly-implanted porousrevision acetabular component in patients undergoing revision total hip arthroplasty

--Manuscript Draft--

Manuscript Number: ARTD-D-19-00024R2

Article Type: Original Research

Keywords: Revision hip arthroplasty; dislocation; instability; cemented dual mobility; fully porousshell

Corresponding Author: Ran Schwarzkopf, MD, MScNYU Hospital for Joint Diseases, NYU Langone Medical CenterNew Rochelle, NY United States

First Author: Jonathan A Gabor, BS

Order of Authors: Jonathan A Gabor, BS

James E Feng, MD

Shashank Gupta, BE

Tyler E Calkins, BS

Craig J Della Valle, MD

Jonathan Vigdorchik, MD

Ran Schwarzkopf, MD MSc

Abstract: Background: The most common indications for revision total hip arthroplasty (rTHA)are instability/dislocation and mechanical loosening. Efforts to address this haveincluded the use of dual mobility (DM) articulations. The aim of this study is to report onthe use of cemented DM cups in complex acetabular rTHA cases with a high risk ofrecurrent instability.

Methods: A multicenter, retrospective study was conducted. Patients who received anovel acetabular construct consisting of a monoblock DM cup cemented into a fullyporous metal shell were included. Outcomes data included 90-day complications andreadmissions, revision for any reason, and Harris Hip Scores.

Results: Thirty-eight hips in 38 patients were included for this study. At a medianfollow-up of 215.5 days (range, 6–783 days), the Harris Hip Score improved from amean of 50 ± 12.2 to 78 ± 11.2 (p<0.001). One (2.6%) patient experienced adislocation on postoperative day 1, and was closed reduced with no furthercomplications. There was one (2.6%) reoperation for periprosthetic joint infectiontreated with a two-stage exchange.

Conclusions: In this complex series of patients, cementation of a monoblock DM cupinto a newly-implanted fully porous revision shell reliably provided solid fixation with alow risk of dislocation at short-term follow-up. While longer term follow-up is needed,utilization of this novel construct should be considered in patients at high risk forinstability.

Powered by Editorial Manager® and ProduXion Manager® from Aries Systems Corporation

Page 2: Arthroplasty Today · Shashank Gupta, BE1 Tyler E. Calkins, BS2 Craig J. Della Valle, MD2 Jonathan Vigdorchik, MD3 Ran Schwarzkopf MD MSc1 Author Affiliations: 1D epa rtm n of OrthopedicSurg

February 25, 2019 Ran Schwarzkopf, MD

Associate Professor, Division of Adult Reconstructive Surgery

Department of Orthopedic Surgery

NYU Langone Health

NYU Langone Orthopedic Hospital (212) 598-6000

[email protected]

Cementation of a Monoblock Dual Mobility Bearing in Patients at High Risk for Dislocation in

Revision Total Hip Arthroplasty

Dear Journal of Arthroplasty,

We present an analysis of our prospectively collected patient-reported outcome data in a manuscript titled,

“Cementation of a Monoblock Dual Mobility Bearing in Patients at High Risk for Dislocation in Revision Total Hip

Arthroplasty.” The aim of this study is to report on the use of cemented DM cups in complex acetabular revision

total hip arthroplasty cases with a high risk of recurrent instability.

We have also included the necessary author forms. The study procedures were reviewed and approved by

the university Institutional Review Board (Study #i17-00535). This manuscript is not currently in review by any

other journal. Thank you for your consideration of our submission.

Respectfully Yours,

Ran Schwarzkopf, MD MSc

Author Contribution

Jonathan A. Gabor, BS Acquisition, analysis, and interpretation of data for the follow-up

report, writing

Shashank Gupta, BE Acquisition, analysis, and interpretation of data for the follow-up

report, writing

James E. Feng, MD Acquisition, analysis, and interpretation of data for the follow-up

report, writing

Tyler E. Calkins, BS Acquisition, analysis, and interpretation of data for the follow-up

report

Craig J. Della Valle, MD Study design, review, edits and approval

Jonathan M. Vigdorchik, MD Study design, review, edits and approval

Ran Schwarzkopf, MD MSc Study design, review, edits and approval

Cover Letter

Page 3: Arthroplasty Today · Shashank Gupta, BE1 Tyler E. Calkins, BS2 Craig J. Della Valle, MD2 Jonathan Vigdorchik, MD3 Ran Schwarzkopf MD MSc1 Author Affiliations: 1D epa rtm n of OrthopedicSurg

Cementation of a monoblock dual mobility bearing in a newly-implanted

porous revision acetabular component in patients undergoing revision total

hip arthroplasty

Jonathan A. Gabor, BS1

James E. Feng, MD1

Shashank Gupta, BE1

Tyler E. Calkins, BS2

Craig J. Della Valle, MD2

Jonathan Vigdorchik, MD3

Ran Schwarzkopf MD MSc1

Author Affiliations: 1Department of Orthopedic Surgery

NYU Langone Health

New York, NY

2Department of Orthopedic Surgery

Rush University Medical Center

Chicago, Illinois

3Adult Reconstruction and Joint Replacement

Hospital for Special Surgery

New York, NY

*Corresponding Author:

Ran Schwarzkopf, MD, MSc

Department of Orthopedic Surgery

NYU Langone Health

301 E 17th St.

New York, NY 10003

Phone: (212) 598-6000

Email: [email protected]

Title Page (WITH Author Details)

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1

Cementation of a monoblock dual mobility bearing in a newly-implanted porous revision 1

acetabular component in patients undergoing revision total hip arthroplasty 2

Abstract 3

Background: The most common indications for revision total hip arthroplasty (rTHA) are 4

instability/dislocation and mechanical loosening. Efforts to address this have included the use of 5

dual mobility (DM) articulations. The aim of this study is to report on the use of cemented DM 6

cups in complex acetabular rTHA cases with a high risk of recurrent instability. 7

Methods: A multicenter, retrospective study was conducted. Patients who received a novel 8

acetabular construct consisting of a monoblock DM cup cemented into a fully porous metal shell 9

were included. Outcomes data included 90-day complications and readmissions, revision for any 10

reason, and Harris Hip Scores. 11

Results: Thirty-eight hips in 38 patients were included for this study. At a median follow-up of 12

215.5 days (range, 6–783 days), the Harris Hip Score improved from a mean of 50 ± 12.2 to 78 ± 13

11.2 (p<0.001). One (2.6%) patient experienced a dislocation on postoperative day 1, and was 14

closed reduced with no further complications. There was one (2.6%) reoperation for 15

periprosthetic joint infection treated with a two-stage exchange. 16

Conclusions: In this complex series of patients, cementation of a monoblock DM cup into a 17

newly-implanted fully porous revision shell reliably provided solid fixation with a low risk of 18

dislocation at short-term follow-up. While longer term follow-up is needed, utilization of this 19

novel construct should be considered in patients at high risk for instability. 20

Keywords 21

Revision hip arthroplasty; dual mobility; cemented dual mobility; dislocation; instability 22

Manuscript (WITHOUT Author Details) Click here to view linked References

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Introduction 23

Revision total hip arthroplasty (rTHA) is a technically challenging surgery with a high 24

risk of complications. Currently, the most common indication for revision and re-revision THA 25

is instability/dislocation, which has been reported to range from 6.6% to as high as 28% of all 26

rTHA patients [1,2,11,3–10]. Management options include the use of large femoral heads, 27

constrained acetabular liners, and dual mobility (DM) articulations. Utilization of a larger 28

femoral head confers stability by increasing the head-to-neck ratio, range of motion (ROM) prior 29

to impingement, and head-jump distance [12]. However, the effects can become diminished with 30

acetabular defects that result in cup placements which deviate from the ideal hip center of 31

rotation [13]. Additionally, larger femoral heads have been associated with increased volumetric 32

wear even with the presence of highly cross-linked polyethylene liners [14]. Finally, because 33

these larger femoral heads may require the use of a thinner liner, there remains the potential for 34

polyethylene fracture and mechanical failure in some cases [15]. Meanwhile, constrained 35

acetabular liners are designed to lock the femoral head into the inner bearing surface, which 36

leads to higher forces on the acetabular cup. Consequently, constrained liners restrict ROM 37

causing prosthetic impingement that can lead to unacceptably high failure rates [16,17], 38

including early catastrophic failures in freshly implanted revision cups. To address some of these 39

shortcomings, DM bearings have been advocated. 40

DM articulations feature an unconstrained tripolar design with two mobile articulations. 41

The first articulation is between the prosthetic head and the inner surface of the polyethylene 42

outer head, and the second is between the outer surface of the polyethylene head and the 43

monoblock metal acetabular shell or metal acetabular liner. At the extremes of ROM, the stem 44

engages the edge of the polyethylene liner, causing it to articulate with the inner surface of the 45

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metal acetabular shell. This design affords the patient a greater impingement-free ROM while 46

enlarging the effective size of the femoral head, conferring the mechanical advantages offered by 47

a larger femoral head jump distance. The current generation of DM implants have shown 48

remarkably low dislocation rates following primary THA and rTHA [18–26]. A recent meta-49

analysis by Levin et al. reported a short- to mid-term dislocation rate of 2.2% following rTHA 50

with the use of DM articulations [27]. Early concerns over excessive early wear due to the 51

additional bearing, aseptic loosening, and intra-prosthetic dislocation (IPD) have been largely 52

alleviated, with an aseptic survivorship rate of 97.7% and aseptic loosening and IPD rates at 53

0.3% and 0.7%, respectively [27]. 54

While biomechanical studies have validated the use of cementation of a DM cup into a 55

well-fixed metal acetabular shell as a viable alternative to a standard cemented polyethylene 56

liner, clinical reports evaluating outcomes of this construct in patients at high risk for recurrent 57

instability and dislocation have been equivocal [22,28–31]. The goal of this study is to analyze 58

the short-term outcomes, and rates of complications, reoperations, and re-revisions of a DM cup 59

meant for cementation cemented into a newly-implanted highly porous revision acetabular shell. 60

Our hypothesis is that this reconstruction construct would decrease the incidence of instability 61

after complex rTHA, without an increase in early construct failure. 62

63

Methods 64

A multi-institutional retrospective study was conducted using clinical data of patients 65

who received a novel rTHA construct that utilized a monoblock DM cup that is intended for 66

insertion with cement (cemented POLARCUP◊, Smith & Nephew, Memphis, TN), cemented into 67

a fully porous revision acetabular component (REDAPT◊, Smith & Nephew, Memphis, TN). 68

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Two institutions contributed the data of 34 patients and 4 patients, respectively, to this study. The 69

study procedures were reviewed and approved by the university Institutional Review Board 70

(Study #i17-00535). 71

Data Collection 72

All institutions participating in this study performed a retrospective chart review of a 73

consecutive cohort of patients who underwent rTHA surgery and received the rTHA construct. 74

Baseline demographics (age, gender, race, and insurance type), preoperative status (body mass 75

index [BMI], and Charlson Comorbidity Index [CCI], laterality, radiographic Paprosky 76

Classification of the acetabular defects, number of previous revision surgeries, time interval from 77

last hip arthroplasty, surgical indication, surgical factors (extended trochanteric osteotomy [ETO] 78

performed, allograft use, number of screws used, concomitant acetabular cage usage, 79

intraoperative complications), and quality outcomes (length of stay, inpatient complications, 30- 80

and 90-day readmissions, all-cause re-revisions) were collected. 81

Patients 82

Thirty-eight patients treated by seven fellowship-trained arthroplasty surgeons between 83

May 2016 and June 2018 were included. All patients who received the POLARCUP◊ cemented 84

into a REDAPT◊ acetabular component over this time period were included in this study. No 85

patients were excluded. The decision was made to use this construct if it was felt by the 86

operating surgeon that the patient would be at a high risk of instability following a complex 87

acetabular reconstruction in which a fully porous acetabular shell was used. Risk was defined by 88

the degree of acetabular bone loss (as defined by the Paprosky classification), as well as the 89

patient history and indication for revision [32]. 90

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The mean patient age was 62.7 ± 9.7 years. There were 18 males (47.4%) and 20 females 91

(52.6%) with a mean body mass index of 29.7 ± 7.0 kg/m2. Patients underwent a mean of 1.6 92

prior reconstructive hip surgeries (range, 1–4), including the primary THA. The mean amount of 93

time between the primary THA and the revision surgery of interest was 12.7 ± 9.2 years. 94

Preoperatively, the majority of patients ambulated with either a rolling walker (13, 34.2%) or 95

cane (16, 42.1%). According to the Paprosky Classification, 4 (10.5%) patients were Type IIA, 96

10 (26.3%) patients were Type IIB, 6 (15.8%) patients were Type IIC, 9 (23.7%) patients were 97

Type IIIA, and 9 (23.7%) patients were Type IIIB [32]. Additional demographics can be found in 98

Table 1. Specific indications for rTHA included 23 (60.5%) patients for aseptic loosening of the 99

acetabulum, 9 (23.7%) for periprosthetic joint infection, 4 (10.5%) for instability, and 2 (5.3%) 100

for malorientation of the acetabular cup and soft tissue impingement. (Table 2). 101

Surgical Technique 102

Twenty-seven (71.1%) cases were performed using a posterior approach and 11 cases 103

(28.9%) were performed using a modified direct lateral approach. Femoral stems were revised in 104

addition to the acetabular components in 20 (52.6%) cases. Extended trochanteric osteotomies 105

were performed to extract well-fixed femoral components in seven (20%) cases. Fresh frozen 106

cancellous allograft was used to fill contained defects in 18 (47.4%) cases, and concomitant 107

acetabular cages were used in 11 (28.9%) cases. Mean surgical time was 208.6 ± 62.9 minutes. 108

The revision shell is unique, offering a combination of locking and non-locking 109

cancellous bone screws. Following final cup insertion, the DM monoblock acetabular cup was 110

then cemented in place, when the cement had reached a doughy consistency (Figure 1). The 111

metal acetabular cup intended for cementation is manufactured from stainless steel. Its backside 112

design features anti-rotation fins as well as 0.35 mm equatorial teeth that further enhance 113

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primary stability. The monoblock dual mobility shell was a minimum of 11 mm smaller in outer 114

diameter than the revision shell utilized. The median porous metal shell size was 60 mm (range, 115

54–76 mm), the median polyethylene outer head size was 47 mm (range, 43–63 mm), and the 116

inner femoral head sizes were 28 mm (in cups ≥47 mm) and 22 mm (43 mm and 45 mm cups). 117

118

Results 119

Thirty-eight patients were available for both clinical and radiographic evaluation at a 120

median follow-up of 215.5 days (range, 6–783 days). There were no intraoperative 121

complications. There were seven (18.4%) inpatient complications. Two (5.3%) were surgical 122

complications and included an anterior hip dislocation on postoperative day 1 in one patient and 123

proximal DVT in another patient. The dislocation was spontaneous and not precipitated by any 124

trauma/falls, and a closed reduction was performed with no complications. At latest follow-up, 125

the patient was doing well with 5/5 abductor strength and had no hip instability since the 126

dislocation. The DVT was treated with heparin and IVC filter placement; heparin was stopped 127

and the patient resumed aspirin therapy for prophylaxis prior to discharge, with no further 128

complications. Five (13.2%) were medical complications and included supraventricular 129

tachycardia, atrial fibrillation, urinary retention, UTI, and myocardial infarction in one patient 130

each. Four (11.8%) patients had postoperative anemia treated with blood transfusion. Additional 131

surgical information can be found in Table 3. 132

The majority of patients were discharged home with health services (26, 68.4%), 133

followed by skilled nursing facilities (9, 23.7%), acute rehabilitation facilities (1, 2.6%), and 134

home with self-care (2, 5.3%). Postoperatively, four (10.5%) patients experienced complications 135

– three (7.9%) within 30 days and one (2.6%) within 90 days following discharge. One patient 136

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experienced a non-displaced fracture of the greater trochanter, which was treated non-137

operatively. Two patients experienced infection – one was treated with an irrigation and 138

debridement due to continued wound drainage, with no further returns to the operating room; the 139

other underwent a two-stage exchange for a periprosthetic joint infection 10 months after the 140

index revision surgery. One patient was admitted for dehydration and acute renal failure; this 141

patient expired due to cardiac complications and so had an orthopedic follow-up time of only six 142

days. 143

The mean Harris Hip Score at last follow-up was 78 (range, 49–95), significantly 144

improved from the mean preoperative score of 50 (range, 35–78) (p < 0.001). At latest 145

radiographic follow-up, there were no dissociations at the DM-cement interface. All outcome 146

information is summarized in Table 4. 147

148

Discussion 149

Recurrent instability is the most common cause of failure requiring repeat revision 150

following rTHA. A number of surgical treatment modalities have been proposed to decrease the 151

incidence of hip instability in high-risk patients, including the use of dual mobility bearings [16]. 152

The unconstrained tripolar design of the DM implant enhances stability by effectively increasing 153

the femoral head size while increasing the ROM to impingement and jump distance needed for 154

dislocation. The long-term survivorship as well as rates of dislocation following rTHA with DM 155

have been excellent [27,33]. However, a fraction of high-risk patients will continue to experience 156

dislocation despite these enhanced implant designs. In these patients, novel constructs may be of 157

unique benefit. In this report, we describe a low risk of dislocation amongst a complex cohort of 158

patients where a novel construct was utilized, including the use of a monoblock DM cup 159

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specifically intended for insertion with cement, cemented into a cementless revision acetabular 160

component. While biomechanical studies have suggested that this type of construct is sound and, 161

in fact, stronger than cemented polyethylene liners which have been commonly used in clinical 162

practice, there has been little clinical data to support the use of this construct [28,34,35]. 163

In many rTHA cases, a well-fixed acetabular shell can be retained; however, all of the 164

cases included in the present study required an acetabular shell revision. Due to the extent of the 165

bone loss and bony defects, it was felt by the operating surgeons that a fully porous revision shell 166

rather than a modular acetabular cup was needed to achieve adequate fixation and reconstruction 167

of the acetabulum. The advantage of using a newly-implanted fully porous shell, aside from the 168

location and number of screw holes and shell porosity, is having the ability to place the 169

acetabular shell in the best reconstruction position possible. However, as this may not be the best 170

position for hip stability, a liner is cemented within the shell in a better “safe-zone” position. The 171

use of cement is necessary as these shells have no locking mechanism. In order to impart greater 172

stability to the construct, the decision was made to use a DM shell rather than a polyethylene 173

liner in these cases. An example of this is shown in Figure 3; the revision shell is placed in over 174

55° of abduction and in a more neutral version in order to achieve good construct fixation, and 175

the DM cup is placed in a more stable fixation around 40° of abduction and 15° of anteversion. 176

To our knowledge, this is the largest US study to date reporting on the clinical outcomes 177

of a cemented DM cup in a newly-implanted fully porous acetabular shell. Our results show that 178

cementation of a DM cup designed for cemented use into a newly-implanted highly porous, 179

revision acetabular shell can lead to enhanced hip stability in the early postoperative period with 180

a low-risk of early dislocation or mechanical failure. One (2.6%) patient experienced a 181

spontaneous dislocation on postoperative day 1, which was closed reduced later that day with no 182

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further recurrence of instability. In our cohort, there were no IPD or failures at the DM-cement 183

interface, nor were there any instances of re-revision for early aseptic loosening. Only one 184

(2.6%) patient required a re-revision with removal of hardware, which was due to a 185

periprosthetic joint infection. However, at the time of explant, all the components were noted to 186

be well-fixed. Evidence of functional improvements in this cohort was demonstrated by 187

significant improvements in hip range of motion, as well as a significant improvement in Harris 188

Hip Scores. 189

Studies on the clinical performance of cemented DM cups have been generally limited, 190

but have been more common in Europe where the use of DM is more widespread. Hamadouche 191

et al. reviewed 47 patients treated with cemented DM cups for recurrent dislocation following 192

primary or revision THA [36]. After a minimum follow-up of 2 years, two patients (4.3%) had 193

further episodes of dislocation, which occurred between the polyethylene outer head and the 194

metal shell in one hip, and the femoral inner head and the outer polyethylene head (IPD) in the 195

other. The authors suspected that improper placement of the acetabular shell in excessive 196

abduction was responsible for the former, and wear and fatigue deformation due to excessive 197

activity was responsible for the latter. A later follow-up study reporting on the 5–13 year results 198

of this cohort was performed [37]. Three patients (5.6%) experienced recurrent dislocation, two 199

of which were intra-prosthetic. The cumulative survival rate at ten years was 86.1% using re-200

dislocation as the end-point, and the authors concluded that DM represents the best 201

reconstructive option for the treatment of recurrent hip instability after THA. Schneider et al. 202

explored the outcomes of 96 rTHAs with cemented DM constructs intended for cement use 203

(Novae Stick, SERF, Décines, France) and acetabular cages. Despite the majority of patients 204

having severe acetabular bone loss, they found a high dislocation rate of 10.4% and an aseptic 205

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survivorship rate of 99.3% at 8 years [29]. Haen et al. found that when there is a moderate 206

deficiency in bone stock, rates of mechanical loosening are comparable regardless of whether an 207

acetabular reinforcement device is used in conjunction with a cemented DM cup [38]. 208

Plummer and colleagues were the first US group to report on the clinical performance of 209

a construct that was similar to the one used in this series [22]. Nine of the 36 revised hips in their 210

series received DM components cemented into well-fixed or new acetabular shells. Of these, two 211

required re-revision due to failure at the DM-cement interface within the first 90 postoperative 212

days. Importantly, these cases utilized a technique that involved roughening the backside of a 213

modular DM liner (modular dual mobility, Stryker, Mahwah, NJ) with a high-speed burr and 214

then cementing it into a shell [22]. The authors, currently, strongly recommend against the use of 215

this technique. At a minimum follow-up of 2 years, no failures had been observed with the other 216

cemented DM cups in their study. Chalmers et al. reviewed the results of 18 patients that had 217

undergone rTHA with a monoblock DM construct cemented into a well-fixed or new acetabular 218

component [30]. At mean follow-up of three years, three patients (17%) experienced 219

postoperative dislocations, and no cups failed at the DM-cement interface. The dislocations 220

occurred at a mean of four months postoperatively. Two were treated with open reduction and 221

one with revision to a cemented constrained liner. Evangelista et al. assessed the outcomes of 18 222

patients who underwent cementation of a DM monoblock cup, designed for cementation, into a 223

well-fixed or new revision acetabular cup [31]. At a mean follow-up of 36 months, there were no 224

cases of hip dislocation nor any dissociations at the DM-cement interface. 225

Though DM implants may present a promising solution for preventing hip instability, a 226

potential disadvantage is their increased cost relative to traditional THA implants [39–41]. 227

However, given the economic burden posed by rTHA procedures, which can exceed $50,000 in 228

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hospital charges alone, the use of DM implants may actually be more cost-effective from a 229

societal perspective, especially in complex rTHA with an increased risk of instability [1]. 230

Our study has several limitations that must be taken into consideration. Only one type of 231

fully porous acetabular shell and DM cup was used in this study, and therefore the results may 232

not be generalizable to other designs and constructs. The cohort of patients in this study was 233

relatively small and the follow-up time was limited. Despite this, the incidence rates of 234

dislocation in both primary and revision THA are highest in the immediate postoperative period 235

and remain elevated throughout the first three postoperative months, which is adequately covered 236

in the present study [42]. Still, further follow-up will be required to ensure long-term durability 237

of this construct. Future studies may be needed to directly compare outcomes between cemented 238

DM cups, constrained liners, and large femoral heads utilized in complex THA revision cases. 239

240

Conclusion 241

Cementation of a DM monoblock cup into a newly-implanted fully porous revision shell 242

was associated with a low risk of surgical complications and re-revision at short-term follow-up. 243

This technique allows for placement of the porous cup such that bony purchase is maximized, 244

and allows for improved placement of the DM cup with regards to abduction, and anteversion, 245

and the hip’s natural center of rotation. Considerations for this construct should be made in 246

patients at high risk of dislocation in order to provide durable fixation and improved stability. 247

248

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References 249

[1] Bozic KJ, Kurtz SM, Lau E, Ong K, Vail TP, Berry DJ. The Epidemiology of Revision 250 Total Hip Arthroplasty in the United States. J Bone Jt Surgery-American Vol 251

2009;91:128–33. doi:10.2106/JBJS.H.00155. 252 [2] Gwam CU, Mistry JB, Mohamed NS, Thomas M, Bigart KC, Mont MA, et al. Current 253

Epidemiology of Revision Total Hip Arthroplasty in the United States: National Inpatient 254 Sample 2009 to 2013. J Arthroplasty 2017;32:2088–92. 255 doi:10.1016/J.ARTH.2017.02.046. 256

[3] Parvizi J, Picinic E, Sharkey PF. Revision total hip arthroplasty for instability: surgical 257 techniques and principles. J Bone Joint Surg Am 2008;90:1134–42. 258

[4] Wetters NG, Murray TG, Moric M, Sporer SM, Paprosky WG, Della Valle CJ. Risk 259 factors for dislocation after revision total hip arthroplasty. Clin Orthop Relat Res 260

2013;471:410–6. doi:10.1007/s11999-012-2561-7. 261 [5] Berend KR, Sporer SM, Sierra RJ, Glassman AH, Morris MJ. Achieving stability and 262

lower-limb length in total hip arthroplasty. J Bone Joint Surg Am 2010;92:2737–52. 263 [6] Alberton GM, High WA, Morrey BF. Dislocation after revision total hip arthroplasty : an 264

analysis of risk factors and treatment options. J Bone Joint Surg Am 2002;84–A:1788–92. 265 [7] Carter AH, Sheehan EC, Mortazavi SMJ, Purtill JJ, Sharkey PF, Parvizi J. Revision for 266

Recurrent Instability. J Arthroplasty 2011;26:46–52. doi:10.1016/j.arth.2011.03.021. 267

[8] Khatod M, Barber T, Paxton E, Namba R, Fithian D. An Analysis of the Risk of Hip 268 Dislocation with a Contemporary Total Joint Registry. Clin Orthop Relat Res 269

2006;447:19–23. doi:10.1097/01.blo.0000218752.22613.78. 270 [9] Mahomed NN, Barrett JA, Katz JN, Phillips CB, Losina E, Lew RA, et al. Rates and 271

outcomes of primary and revision total hip replacement in the United States medicare 272

population. J Bone Joint Surg Am 2003;85–A:27–32. 273

[10] Weiss RJ, Beckman MO, Enocson A, Schmalholz A, Stark A. Minimum 5-Year Follow-274 Up of a Cementless, Modular, Tapered Stem in Hip Revision Arthroplasty. J Arthroplasty 275 2011;26:16–23. doi:10.1016/j.arth.2009.11.009. 276

[11] Springer BD, Fehring TK, Griffin WL, Odum SM, Masonis JL. Why revision total hip 277 arthroplasty fails. Clin Orthop Relat Res 2009;467:166–73. doi:10.1007/s11999-008-278

0566-z. 279 [12] Garbuz DS, Masri BA, Duncan CP, Greidanus N V, Bohm ER, Petrak MJ, et al. The 280

Frank Stinchfield Award: Dislocation in revision THA: do large heads (36 and 40 mm) 281 result in reduced dislocation rates in a randomized clinical trial? Clin Orthop Relat Res 282 2012;470:351–6. doi:10.1007/s11999-011-2146-x. 283

[13] Halley D, Glassman A, Crowninshield RD. Recurrent dislocation after revision total hip 284

replacement with a large prosthetic femoral head. A case report. J Bone Jt Surg 2004;86–285 A:827–30. 286

[14] Lachiewicz PF, Soileau ES, Martell JM. Wear and Osteolysis of Highly Crosslinked 287

Polyethylene at 10 to 14 Years: The Effect of Femoral Head Size. Clin Orthop Relat Res 288 2016;474:365–71. doi:10.1007/s11999-015-4319-5. 289

[15] Tower SS, Currier JH, Currier BH, Lyford KA, Van Citters DW, Mayor MB. Rim 290 Cracking of the Cross-Linked Longevity Polyethylene Acetabular Liner After Total Hip 291 Arthroplasty. J Bone Jt Surg 2007;89:2212. doi:10.2106/JBJS.F.00758. 292

[16] Guyen O. Constrained liners, dual mobility or large diameter heads to avoid dislocation in 293

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THA. EFORT Open Rev 2016;1:197–204. doi:10.1302/2058-5241.1.000054. 294

[17] Berend KR, Lombardi A V., Mallory TH, Adams JB, Russell JH, Groseth KL. The Long-295 term Outcome of 755 Consecutive Constrained Acetabular Components in Total Hip 296 Arthroplasty: Examining the Successes and Failures. J Arthroplasty 2005;20:93–102. 297

doi:10.1016/J.ARTH.2005.06.001. 298 [18] Dangin A, Boulat S, Farizon F, Philippot R. Prevention of Dislocation Risk During Hip 299

Revision Surgery with the Dual Mobility Concept; Study of a New Generation of Dual 300 Mobility Cups. Surg Technol Int 2016;29:314–9. 301

[19] Harwin SF, Sultan AA, Khlopas A, Chughtai M, Sodhi N, Piuzzi NS, et al. Mid-Term 302

Outcomes of Dual Mobility Acetabular Cups for Revision Total Hip Arthroplasty. J 303 Arthroplasty 2018;33:1494–500. doi:10.1016/j.arth.2017.12.008. 304

[20] Jauregui JJ, Pierce TP, Elmallah RK, Cherian JJ, Delanois RE, Mont MA. Dual Mobility 305 Cups: An Effective Prosthesis in Revision Total Hip Arthroplasties for Preventing 306

Dislocations. HIP Int 2016;26:57–61. doi:10.5301/hipint.5000295. 307 [21] Lange JK, Spiro SK, Westrich GH. Utilizing Dual Mobility Components for First-Time 308

Revision Total Hip Arthroplasty for Instability. J Arthroplasty 2018;33:505–9. 309 doi:10.1016/j.arth.2017.09.029. 310

[22] Plummer DR, Christy JM, Sporer SM, Paprosky WG, Della Valle CJ. Dual-Mobility 311 Articulations for Patients at High Risk for Dislocation. J Arthroplasty 2016;31:131–5. 312 doi:10.1016/J.ARTH.2016.03.021. 313

[23] Prudhon JL, Steffann F, Ferreira A, Verdier R, Aslanian T, Caton J. Cementless dual-314 mobility cup in total hip arthroplasty revision. Int Orthop 2014;38:2463–8. 315

doi:10.1007/s00264-014-2448-1. 316 [24] Snir N, Park BK, Garofolo G, Marwin SE. Revision of Failed Hip Resurfacing and Large 317

Metal-on-Metal Total Hip Arthroplasty Using Dual-Mobility Components. Orthopedics 318

2015;38:369–74. doi:10.3928/01477447-20150603-04. 319

[25] Stucinskas J, Kalvaitis T, Smailys A, Robertsson O, Tarasevicius S. Comparison of dual 320 mobility cup and other surgical construts used for three hundred and sixty two first time 321 hip revisions due to recurrent dislocations: five year results from Lithuanian arthroplasty 322

register. Int Orthop 2018;42:1015–20. doi:10.1007/s00264-017-3702-0. 323 [26] Sutter EG, McClellan TR, Attarian DE, Bolognesi MP, Lachiewicz PF, Wellman SS. 324

Outcomes of Modular Dual Mobility Acetabular Components in Revision Total Hip 325 Arthroplasty. J Arthroplasty 2017;32:S220–4. doi:10.1016/j.arth.2017.03.035. 326

[27] Levin JM, Sultan AA, O’Donnell JA, Sodhi N, Khlopas A, Piuzzi NS, et al. Modern Dual-327 Mobility Cups in Revision Total Hip Arthroplasty: A Systematic Review and Meta-328 analysis. J Arthroplasty 2018. doi:10.1016/J.ARTH.2018.08.013. 329

[28] Wegrzyn J, Thoreson AR, Guyen O, Lewallen DG, An K-N. Cementation of a dual-330

mobility acetabular component into a well-fixed metal shell during revision total hip 331 arthroplasty: A biomechanical validation. J Orthop Res 2013;31:991–7. 332 doi:10.1002/jor.22314. 333

[29] Schneider L, Philippot R, Boyer B, Farizon F. Revision total hip arthroplasty using a 334 reconstruction cage device and a cemented dual mobility cup. Orthop Traumatol Surg Res 335 2011;97:807–13. doi:10.1016/J.OTSR.2011.09.010. 336

[30] Chalmers BP, Ledford CK, Taunton MJ, Sierra RJ, Lewallen DG, Trousdale RT. 337 Cementation of a Dual Mobility Construct in Recurrently Dislocating and High Risk 338 Patients Undergoing Revision Total Arthroplasty. J Arthroplasty 2018;33:1501–6. 339

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14

doi:10.1016/J.ARTH.2017.11.055. 340

[31] Evangelista P, Okroj K, Plummer D, Della Valle C, Schwarzkopf R. Do Cemented Dual-341 Mobility Cups Confer Stability for Patients at High Risk of Dislocation in Revision Total 342 Hip Arthroplasty? J Hip Surg 2018;02:088–91. doi:10.1055/s-0038-1661341. 343

[32] Paprosky WG, Perona PG, Lawrence JM. Acetabular defect classification and surgical 344 reconstruction in revision arthroplasty: A 6-year follow-up evaluation. J Arthroplasty 345 1994;9:33–44. doi:10.1016/0883-5403(94)90135-X. 346

[33] Bauchu P, Bonnard O, Cyprès A, Fiquet A, Girardin P, Noyer D. The dual-mobility 347 POLARCUP: first results from a multicenter study. Orthopedics 2008;31. 348

[34] Beaulé PE, Ebramzadeh E, Le Duff M, Prasad R, Amstutz HC. Cementing a liner into a 349 stable cementless acetabular shell: the double-socket technique. J Bone Joint Surg Am 350 2004;86–A:929–34. 351

[35] Callaghan JJ, Parvizi J, Novak CC, Bremner B, Shrader W, Lewallen DG, et al. A 352

constrained liner cemented into a secure cementless acetabular shell. J Bone Joint Surg 353 Am 2004;86–A:2206–11. 354

[36] Hamadouche M, Biau DJ, Huten D, Musset T, Gaucher F. The use of a cemented dual 355 mobility socket to treat recurrent dislocation. Clin Orthop Relat Res 2010;468:3248–54. 356

doi:10.1007/s11999-010-1404-7. 357 [37] Hamadouche M, Ropars M, Rodaix C, Musset T, Gaucher F, Biau D, et al. Five to thirteen 358

year results of a cemented dual mobility socket to treat recurrent dislocation. Int Orthop 359

2017;41:513–9. doi:10.1007/s00264-016-3343-8. 360 [38] Haen TX, Lonjon G, Vandenbussche E. Can cemented dual-mobility cups be used without 361

a reinforcement device in cases of mild acetabular bone stock alteration in total hip 362 arthroplasty? Orthop Traumatol Surg Res 2015;101:923–7. 363 doi:10.1016/J.OTSR.2015.09.027. 364

[39] Orthopedic Network News. 2015 Hip and knee implant review 2015. 365

https://www.orthopedicnetworknews.com/archives/onn263s1.pdf (accessed March 14, 366 2019). 367

[40] Barlow BT, McLawhorn AS, Westrich GH. The Cost-Effectiveness of Dual Mobility 368

Implants for Primary Total Hip Arthroplasty. J Bone Jt Surg 2017;99:768–77. 369 doi:10.2106/JBJS.16.00109. 370

[41] Rudy HL, Padilla JA, Gabor JA, Iorio R, Schwarzkopf R, Vigdorchik J. Cost-371 Effectiveness of Dual Mobility and a Value-Based Algorithm of Utilization. Orthop Clin 372

North Am 2019;50:151–8. doi:10.1016/J.OCL.2018.11.002. 373 [42] Phillips CB, Barrett JA, Losina E, Mahomed NN, Lingard EA, Guadagnoli E, et al. 374

Incidence rates of dislocation, pulmonary embolism, and deep infection during the first six 375 months after elective total hip replacement. J Bone Joint Surg Am 2003;85–A:20–6. 376

377

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Table 1: Baseline Patient Demographics (n = 38)

Age (years) 62.7 ± 9.7 Gender Male 18 (47.4%) Female 20 (52.6%) BMI 29.7 ± 7.0 Race African American (Black) 8 (21.1%) Asian 1 (2.6%) White 22 (57.9%) Other 5 (13.2%) ASA 1 0 (0.0%) 2 16 (42.1%) 3 20 (52.6%) 4 2 (5.3%) Charlson Comorbidity Index 2.8 ± 1.6 Smoking Status Current Smoker 5 (13.2%) Former Smoker 17 (44.7%) Never Smoker 16 (42.1%) Marital Status Married 11 (28.9%) Divorced 3 (7.9%) Single 15 (39.5%) Other 9 (23.7%) Insurance Type Commercial 12 (31.6%) Medicare 16 (42.1%) Medicaid 8 (21.1%) Workers Comp 2 (5.3%) Laterality Left 17 (44.7%) Right 21 (55.3%) Previous Reconstructive Surgeries 1.6 ± 0.8 Paprosky Classification IIA 4 (10.5%) IIB 10 (26.3%) IIC 6 (15.8%) IIIA 9 (23.7%) IIIB 9 (23.7%) Preoperative Ambulatory Status Rolling Walker 13 (34.2%) Cane 16 (42.1%) Crutches 2 (5.3%) Unassisted 5 (13.2%) Unknown 2 (5.3%) Mean Time from Primary to Revision (years) 12.7 ± 9.2

Table 1

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Table 2: Indication for revision THA of interest (n = 38)

Aseptic Loosening 23 (60.5%)

Septic Failure 9 (23.7%)

Instability 4 (10.5%)

Malorientation of the acetabular cup 2 (5.3%)

Table 2

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Table 3: Surgical Information (n = 38) Anesthesia Type

General 30 (68.4%) Regional (Spinal/Epidural) 8 (21.1%) Surgeon

Surgeon 1 1 (2.6%) Surgeon 2 1 (2.6%) Surgeon 3 11 (28.9%) Surgeon 4 14 (36.8%) Surgeon 5 2 (5.3%) Surgeon 6 5 (13.2%) Surgical Time (minutes) 208.6 ± 62.9 Median Porous Metal Shell Size (mm) 62 (54 – 76) Median Number of Screws 5 (3 – 14) Median Dual Mobility Outer Cup Size (mm)

48 (43 – 63)

Median Femoral Head Size (mm) 28 (22 – 28)

Femoral stem revised 20 (52.6%) Bone Allograft Used

Yes 18 (47.4%) No 18 (47.4%) Unknown 2 (5.3%) Extended Trochanteric Osteotomy

Yes 7 (18.4%) No 31 (81.6%) Acetabular Cage Construct Used

Yes 11 (28.9%) No 27 (71.1%) Intraoperative Complications 0 (0.0%) Inpatient Complications 7 (18.4%)

Medical 5 (13.2%)

Patient 5 - Supraventricular tachycardia Patient 22 - UTI Patient 28 - Atrial fibrillation Patient 34 - Urinary retention Patient 36 - Myocardial infarction

Surgical 2 (5.3%) Patient 13 - DVT Patient 37 - Anterior hip dislocation on POD1

Postoperative Anemia Requiring Blood Transfusion

4 (10.5%)

Length of Stay (days) 4.7 ± 2.9

Table 3

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Table IV. Outcomes (n = 38) Median follow-up (days) 215.5 (range, 6–783) Discharge Disposition Home or Self-Care 2 (5.3%)

Home with Health Services

26 (68.4%)

Skilled Nursing Facility 9 (23.7%)

Acute Rehabilitation Facility

1 (2.6%)

Inpatient Complications 7 (18.4%)

30-Day Complications 3 (7.9%) Patient 11 - Hip pain, x-ray showed avulsion fracture of the greater trochanter Patient 32* - Hip pain/drainage; treated with irrigation and debridement Patient 36* - Dehydration and acute renal failure

Readmissions 2 (5.3%)

90-Day Complications 1 (2.6%) Patient 24* - Irrigation and debridement of hip wound

Readmissions 1 (2.6%)

Re-Revisions 1 (2.6%)

Patient 28 - Removal of hardware Deep Infection 1 (2.6%)

Dislocation 0 (0.0%)

Aseptic Loosening 0 (0.0%)

Ambulatory Status at Latest Follow-Up Rolling Walker 11 (28.9%) Cane 13 (34.2%) Crutches 1 (2.6%) Unassisted 12 (31.6%) Unknown 1 (2.6%)

*Resulted in hospital readmission

Table 4

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Figure 1: (A) POLARCUP

◊ intended for cementation prior to implantation. (B) REDAPT

◊ fully

porous shell impacted in place following acetabular preparation. (C) Trial placement of DM

monoblock cup. (D) DM cup cemented into revision acetabular shell.

Figure 1

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Figure 2: Pre-/postoperative pelvic radiographs.

Figure 2

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Figure 3: Representative example of a fully porous acetabular shell implanted in a position for

maximum bony coverage but less than ideal for hip stability (abduction >55°, anteversion <10°)

with the DM cup cemented within in a better position for hip stability.

Figure 3

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COMBINED, BLINDED CONFLICT OF INTEREST STATEMENT American Association of Hip and Knee Surgeons

(Adopted from the American Academy of Orthopaedic Surgeons disclosure statement)

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Smith and Nephew: IP royalties 2. Speakers bureau/paid presentations for a company or supplier (The following conflicts were disclosed)

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Orthophor: Stock or stock Options’ Intellijoint: Paid consultant Gauss Surgical: Paid consultant PSI: Paid consultant

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JOA: Editorial or governing board Arthroplasty today: Editorial or governing board

9. Board member/committee appointments for a society (The following conflicts were disclosed) American Association of Hip and Knee Surgeons: Board or committee member

Arthritis Foundation: Board or committee member DePuy: Board or committee member Hip Society: Board or committee member Knee Society: Board or committee member Mid America Orthopaedic Association: Board or committee member Orthopedics Today: Board or committee member American Association of Hip and Knee Surgeons: Board or committee member AAOS: Board or committee member

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INDIVIDUAL CONFLICT OF INTEREST STATEMENT American Association of Hip and Knee Surgeons

(Adopted from the American Academy of Orthopaedic Surgeons disclosure statement)

The following form must be filled out completely and submitted by each author (example, 6 authors, 6 forms). All items require a response. If there is no relevant disclosure for a given item, enter "None.”

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Each author must sign AND print or type his/her name, date and submit a separate form In addition, one BLINDED Conflict of Interest form (no author names used) should be submitted per manuscript with all author disclosures. Jonathan A. Gabor Jonathan A. Gabor January 17, 2019

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INDIVIDUAL CONFLICT OF INTEREST STATEMENT American Association of Hip and Knee Surgeons

(Adopted from the American Academy of Orthopaedic Surgeons disclosure statement)

The following form must be filled out completely and submitted by each author (example, 6 authors, 6 forms). All items require a response. If there is no relevant disclosure for a given item, enter "None.”

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1. Royalties from a company or supplier (The following conflicts were disclosed) None 2. Speakers bureau/paid presentations for a company or supplier (The following conflicts were disclosed) None 3A. Paid employee for a company or supplier (The following conflicts were disclosed) None 3B. Paid consultant for a company or supplier (The following conflicts were disclosed) None 3C. Unpaid consultants for a company or supplier (The following conflicts were disclosed) None 4. Stock or stock options in a company or supplier (The following conflicts were disclosed) None 5. Research support from a company or supplier as a Principal Investigator (The following conflicts were disclosed) None 6. Other financial or material support from a company or supplier (The following conflicts were disclosed) None 7. Royalties, financial or material support from publishers (The following conflicts were disclosed) None 8. Medical/Orthopaedic publications editorial/governing board (The following conflicts were disclosed) None 9. Board member/committee appointments for a society (The following conflicts were disclosed) None

Each author must sign AND print or type his/her name, date and submit a separate form In addition, one BLINDED Conflict of Interest form (no author names used) should be submitted per manuscript with all author disclosures. Shashank Gupta, January 17, 2019

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INDIVIDUAL CONFLICT OF INTEREST STATEMENT American Association of Hip and Knee Surgeons

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The following form must be filled out completely and submitted by each author (example, 6 authors, 6 forms). All items require a response. If there is no relevant disclosure for a given item, enter "None.”

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INDIVIDUAL CONFLICT OF INTEREST STATEMENT American Association of Hip and Knee Surgeons

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The following form must be filled out completely and submitted by each author (example, 6 authors, 6 forms). All items require a response. If there is no relevant disclosure for a given item, enter "None.”

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Author Name (Print or Type) Author Signature Date

*Conflict of Interest Statement

Page 31: Arthroplasty Today · Shashank Gupta, BE1 Tyler E. Calkins, BS2 Craig J. Della Valle, MD2 Jonathan Vigdorchik, MD3 Ran Schwarzkopf MD MSc1 Author Affiliations: 1D epa rtm n of OrthopedicSurg

INDIVIDUAL CONFLICT OF INTEREST STATEMENT American Association of Hip and Knee Surgeons

(Adopted from the American Academy of Orthopaedic Surgeons disclosure statement)

The following form must be filled out completely and submitted by each author (example, 6 authors, 6 forms). All items require a response. If there is no relevant disclosure for a given item, enter "None.”

Manuscript Title

1. Royalties from a company or supplier (The following conflicts were disclosed) Zimmer Biomet, Smith and Nephew 2. Speakers bureau/paid presentations for a company or supplier (The following conflicts were disclosed) None 3A. Paid employee for a company or supplier (The following conflicts were disclosed) None 3B. Paid consultant for a company or supplier (The following conflicts were disclosed) Depuy, Smith and Nephew, Zimmer Biomet 3C. Unpaid consultants for a company or supplier (The following conflicts were disclosed) none 4. Stock or stock options in a company or supplier (The following conflicts were disclosed) Parvizi Surgical Innovations, Orthophor 5. Research support from a company or supplier as a Principal Investigator (The following conflicts were disclosed) Smith and Nephew, Stryker, Zimmer Biomet, CD Diagnostics 6. Other financial or material support from a company or supplier (The following conflicts were disclosed) none 7. Royalties, financial or material support from publishers (The following conflicts were disclosed) SLACK, Wolter Kluwer, Smith and Nephew, Zimmer Biomet 8. Medical/Orthopaedic publications editorial/governing board (The following conflicts were disclosed) Orthopedics Today 9. Board member/committee appointments for a society (The following conflicts were disclosed) American Association of Hip and Knee Surgeons, Arthritis Foundation, DePuy, Hip Society, Knee Society, Mid America Orhtopaedic Association, Orthopedics Today

Each author must sign AND print or type his/her name, date and submit a separate form In addition, one BLINDED Conflict of Interest form (no author names used) should be submitted per manuscript with all author disclosures. Craig Della Valle Craig Della Valle 1-16-19

Author Name (Print or Type) Author Signature Date

*Conflict of Interest Statement

Page 32: Arthroplasty Today · Shashank Gupta, BE1 Tyler E. Calkins, BS2 Craig J. Della Valle, MD2 Jonathan Vigdorchik, MD3 Ran Schwarzkopf MD MSc1 Author Affiliations: 1D epa rtm n of OrthopedicSurg

INDIVIDUAL CONFLICT OF INTEREST STATEMENT American Association of Hip and Knee Surgeons

(Adopted from the American Academy of Orthopaedic Surgeons disclosure statement)

The following form must be filled out completely and submitted by each author (example, 6 authors, 6 forms). All items require a response. If there is no relevant disclosure for a given item, enter "None.”

Manuscript Title

1. Royalties from a company or supplier (The following conflicts were disclosed) 2. Speakers bureau/paid presentations for a company or supplier (The following conflicts were disclosed) 3A. Paid employee for a company or supplier (The following conflicts were disclosed) 3B. Paid consultant for a company or supplier (The following conflicts were disclosed) Intellijoint Corin 3C. Unpaid consultants for a company or supplier (The following conflicts were disclosed) 4. Stock or stock options in a company or supplier (The following conflicts were disclosed) 5. Research support from a company or supplier as a Principal Investigator (The following conflicts were disclosed) 6. Other financial or material support from a company or supplier (The following conflicts were disclosed) 7. Royalties, financial or material support from publishers (The following conflicts were disclosed) 8. Medical/Orthopaedic publications editorial/governing board (The following conflicts were disclosed) 9. Board member/committee appointments for a society (The following conflicts were disclosed)

Each author must sign AND print or type his/her name, date and submit a separate form In addition, one BLINDED Conflict of Interest form (no author names used) should be submitted per manuscript with all author disclosures. Jonathan Vigdorchik JV 1-9-2019

Author Name (Print or Type) Author Signature Date

*Conflict of Interest Statement

Page 33: Arthroplasty Today · Shashank Gupta, BE1 Tyler E. Calkins, BS2 Craig J. Della Valle, MD2 Jonathan Vigdorchik, MD3 Ran Schwarzkopf MD MSc1 Author Affiliations: 1D epa rtm n of OrthopedicSurg

INDIVIDUAL CONFLICT OF INTEREST STATEMENT American Association of Hip and Knee Surgeons

(Adopted from the American Academy of Orthopaedic Surgeons disclosure statement)

The following form must be filled out completely and submitted by each author (example, 6 authors, 6 forms). All items require a response. If there is no relevant disclosure for a given item, enter "None.”

Encouraging Short Term Outcomes with a Novel Acetabular Reconstruction Construct

Manuscript Title

1. Royalties from a company or supplier (The following conflicts were disclosed) none 2. Speakers bureau/paid presentations for a company or supplier (The following conflicts were disclosed) none 3A. Paid employee for a company or supplier (The following conflicts were disclosed) none 3B. Paid consultant for a company or supplier (The following conflicts were disclosed) Smith&Nephew, Intelijoint 3C. Unpaid consultants for a company or supplier (The following conflicts were disclosed) none 4. Stock or stock options in a company or supplier (The following conflicts were disclosed) Intelijoint, Gauss Surgical, PSI 5. Research support from a company or supplier as a Principal Investigator (The following conflicts were disclosed) Smith&Nephew 6. Other financial or material support from a company or supplier (The following conflicts were disclosed) none 7. Royalties, financial or material support from publishers (The following conflicts were disclosed) none 8. Medical/Orthopaedic publications editorial/governing board (The following conflicts were disclosed) JOA, Arthroplasty today 9. Board member/committee appointments for a society (The following conflicts were disclosed) AAHKS, AAOS

Each author must sign AND print or type his/her name, date and submit a separate form In addition, one BLINDED Conflict of Interest form (no author names used) should be submitted per manuscript with all author disclosures.

Ran Schwarzkopf Ran Schwarzkopf 1/9/2019

Author Name (Print or Type) Author Signature Date

*Conflict of Interest Statement

Page 34: Arthroplasty Today · Shashank Gupta, BE1 Tyler E. Calkins, BS2 Craig J. Della Valle, MD2 Jonathan Vigdorchik, MD3 Ran Schwarzkopf MD MSc1 Author Affiliations: 1D epa rtm n of OrthopedicSurg

Response to reviewers’ comments 4/15/2019

We would like to thank the reviewers for their time and effort helping us improve this work and prepare

it for publication.

Reviewer #1: The authors addressed my comments and concerns appropriately.

Response:

Thank you

Reviewer #2: I appreciate the effort the authors have put forth to make this a better paper, but still have some

suggestions/questions:

1. Line 82: Were all cases performed by one surgeon or a number of different surgeons?

Response: Cases were performed by seven surgeons. This has been clarified in the text below.

Lines 82-83: Thirty-eight patients treated by seven fellowship-trained arthroplasty surgeons between

May 2016 and June 2018 were included.

2. Lines 134-141: Which of the four complications happened within 30 days, and which one happened within

90 days following discharge?

Response: Although this distinction was not made in the text, this information can be found in Table

4. The corresponding section of Table 4 has been copied below.

30-day complications

Patient 11 - Hip pain, x-ray

showed avulsion fracture of the

greater trochanter

Patient 32* - Hip pain/drainage;

treated with irrigation and

debridement

Patient 36* - Dehydration and

acute renal failure

90-day complications Patient 24* - Irrigation and

debridement of hip wound

3. Lines 171-172: Why do the authors think the stability obtained in their study could not have been obtained

with uncemented, modular DM cups? The authors should compare the survivorship/outcomes or rates of

dislocation of uncemented DM cups in rTHA reported in literature to their study.

Detailed Response to Reviewers

Page 35: Arthroplasty Today · Shashank Gupta, BE1 Tyler E. Calkins, BS2 Craig J. Della Valle, MD2 Jonathan Vigdorchik, MD3 Ran Schwarzkopf MD MSc1 Author Affiliations: 1D epa rtm n of OrthopedicSurg

Response: We do not think that the hip stability/risk of dislocation could not have been achieved

with the use of uncemented DM cups; we agree completely with the reviewer that any DM cup

placed in the proper position would achieve the same hip stability. The surgeons that performed

these cases thought they need to use a fully porous acetabular cup in order to achieve proper implant

fixation and decrease the risk of construct failure of fixation (due to increased screw fixation/hole

options and fixation stability achieved with fully porous cups). In these cases, due to the decision to

use these fully porous cups, the surgeons are forced to cement a liner, as there is no locking

mechanism; that’s why a cemented DM was chosen and not an uncemented one. There is no claim

that cemented DM perform better than uncemented DM cups, placed in the same position, in hip

stability/dislocation.

Lines 162-174: In many rTHA cases, a well-fixed acetabular shell can be retained or a modular

acetabular cup used; however, all of the cases included in the present study required an acetabular

shell revision. Due to the extent of the bone loss and bony defects, it was felt by the operating

surgeons that a fully porous revision shell rather than a modular acetabular cup was needed to

achieve adequate fixation and reconstruction of the acetabulum. The advantage of using a newly-

implanted fully porous shell, aside from the location and number of screw holes and shell porosity, is

having the ability to place the acetabular shell in the best reconstruction position possible. However,

as this may not be the best position for hip stability, a liner is cemented within the shell in a better

“safe-zone” position. The use of cement is necessary as these shells have no locking mechanism. In

order to impart greater hip stability to the construct, the decision was made to use a DM shell rather

than a polyethylene liner in these cases. An example of this is shown in Figure 3; the revision shell is

placed in over 55° of abduction and in a more neutral version in order to achieve good construct

fixation, and the DM cup is placed in a more stable fixation around 40° of abduction and 15° of

anteversion.

4. Lines 165-168: Is this more of a technique in the hands of the authors? If so, it should be stated as such.

Certainly, joint reconstruction surgeons have done revision cases before this study placing the acetabular

Page 36: Arthroplasty Today · Shashank Gupta, BE1 Tyler E. Calkins, BS2 Craig J. Della Valle, MD2 Jonathan Vigdorchik, MD3 Ran Schwarzkopf MD MSc1 Author Affiliations: 1D epa rtm n of OrthopedicSurg

components in the best position (with and without adjuncts), and still obtaining good stability and fixation

without using cemented DM cups. A short term follow up study of 6-783 days might not be long enough to

see the effects/failures of potentially implanting malpositioned cups for excellent bony coverage and fixation

and correcting for the malpositioning by using cemented DM cups.

Response: Many surgeons have used fully porous cups to achieve acetabular construct fixation since

the Zimmer TM revision shell was introduced to the market nearly 20 years ago. When using the TM

revision shell, and now the Smith & Nephew Redapt shell, the surgeon must cement a liner as neither

cup has a locking mechanism. Until recently, reports have only described the use of these shells in

combination with regular cemented polyethylene liners. We report here the first series of cementing

a DM cup instead of a polyethylene liner, thus presenting a construct that benefits from a known

fixation technique (use of a fully porous cup) and the stability of a DM articulation.

5. Can the authors include the longest follow up representative x-rays of shell(s) implanted in less than ideal

position for maximum bony coverage.

Response: We have added a new figure with a revision cup placed in over 55° of abduction and in

neutral version in order to achieve good construct fixation and the DM cup is placed in a more stable

fixation around 40° of abduction and 15° of anteversion. The follow-up time for this case is

approximately 2.5 years.

Page 37: Arthroplasty Today · Shashank Gupta, BE1 Tyler E. Calkins, BS2 Craig J. Della Valle, MD2 Jonathan Vigdorchik, MD3 Ran Schwarzkopf MD MSc1 Author Affiliations: 1D epa rtm n of OrthopedicSurg

6. Can this cemented DM cup be used with shells from other companies or stems from other companies? If

not, can the authors explain why not.

Response: Yes, the Polar DM cemented acetabular shell can be used as a primary cemented cup, and

can be cemented into any acetabular construct such as a cage, other fully porous acetabular cups, etc.

Any stem can be used with the proper head, which can be placed into the outer polyethylene DM

head. Mixing inner and outer heads by different companies in DM is not recommended and an off-

label use, but is still done by many revision surgeons.


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