Safety and effectiveness of minimally invasive sacroiliac joint fusion in women with persistent post-partum posterior pelvic girdle pain: 12-month outcomes from a prospective, multi-center trial
© Capobianco et al. 2015
Received: 3 September 2015
Accepted: 21 September 2015
Published: 5 October 2015
Postpartum posterior pelvic girdle pain (PPGP) affects nearly 20 % of women who experience back pain in the peripartum period. The sacroiliac joint is a source of this pain in 75 % of women with persistent PPGP. A subset of women will fail to obtain acceptable pain relief from the current array of non-surgical treatment options. The purpose of this study is to assess the safety and effectiveness of minimally invasive sacroiliac (SI) joint fusion in women with chronic SI joint dysfunction whose pain began in the peri-partum period whose symptoms were recalcitrant to non-surgical management. A sub-group analysis of subjects with sacroiliac joint disruption and/or degenerative sacroiliitis enrolled in a prospective, multi-center trial of SI joint fusion was performed. Subjects with PPGP were identified and compared with women without PPGP and with men. Of 172 enrolled subjects, 52 were male, 100 were females without PPGP and 20 females had PPGP. PPGP subjects were significantly younger (43.3 years, vs. 52.8 for females without PPGP and 50.5 for men, p = 0.002). There were no differences in any other demographic or baseline clinical measure. Women with PPGP experienced a significant improvement in pain (−51 mm on VAS), function (−20.6 pts on ODI) and quality of life (SF-36 PCS +10.4, MCS +7.2, EQ-5D +0.31) at 12 months after surgery. These improvements were characteristic of the overall study results; no difference was detected between sub-groups. The sacroiliac joint can be a source of pain in women with persistent PPGP and should be investigated as a pain generator. In this study, women with carefully diagnosed chronic SI joint pain from PPGP recalcitrant to conservative therapies experienced clinically beneficially improvements in pain, disability and quality of life after minimally invasive SI joint fusion using a series of triangular porous plasma spray coated implants.
KeywordsSacroiliac joint fusion Postpartum pelvic girdle pain Sacroiliac joint dysfunction Sacroiliac joint disruption Degenerative sacroiliitis
Pelvic girdle pain (PGP) is a term used to describe pregnancy-related pain in the sacroiliac joint (SIJ), lumbosacral region, pubic symphysis, or in any combination of these joints. PGP is widespread, affecting nearly half of all pregnant women (Vleeming et al. 2008; Wu et al. 2004). PGP can be distinguished from pregnancy related low back pain (PLBP) by its character, intensity, and location; PLBP is mainly described as a “dull ache” in the lumbar region while PGP is mostly described as pain between the posterior iliac crest and gluteal fold that may radiate into the thigh (Gutke et al. 2008; Vermani et al. 2010). While PGP will resolve in most women within 4 months after giving birth, approximately 20 % of women will experience persistent symptoms, regardless of culture or economic condition (Aldabe et al. 2012; Björklund and Bergström 2000; Ostgaard and Andersson 1992). Pelvic girdle pain that begins during pregnancy and does not resolve, or pain that develops soon after pregnancy is termed postpartum pelvic girdle pain (PPGP) (Vermani et al. 2010).
The exact underlying pathophysiology of PPGP remains unclear, although the most likely explanation is a combination of hormonal and biomechanical factors (Vermani et al. 2010). Hypermobility and ligamentous laxity of the SI joint due to increased levels of estrogen and relaxin appear in the third trimester of pregnancy (Dreyfuss et al. 2004). These altered hormonal factors allow the pelvic girdle to slightly expand in order to accommodate parturition. The most noticeable joint changes (identified radiographically) occur in the pubic symphysis. The joint widens and vertically shifts during pregnancy and delivery, with subsequent reduction after delivery (Björklund et al. 1999). Interestingly, neither increased relaxin levels peripartum nor degree of symphyseal distention have been shown to be a factors in the development of pelvic girdle pain (Aldabe et al. 2012; Björklund et al. 1999). Factors that have been shown to increase the risk of pelvic girdle pain include pre-pregnancy back pain (Sjödahl et al. 2013), back flexor weakness (Gutke et al. 2008), body mass index (Sjödahl et al. 2013), hypermobility, asymmetric SI joint ligament laxity (Damen et al. 2001), emotional distress (Bjelland et al. 2013), and vaginal delivery (Bjelland et al. 2013).
The current array of non-surgical PPGP treatments include medication optimization, physical therapy, and an individualized exercise regimen focused on pelvic stabilization (Vleeming et al. 2008). The European Guidelines for the Diagnosis and Treatment of Pelvic Girdle Pain do not recommend radiofrequency denervation; intra-articular SIJ injections are recommended only in the presence of ankylosing spondylitis (Vleeming et al. 2008). Neither of these have been specifically studied in the PPGP population.
Minimally invasive (MIS) SI joint fusion is an increasingly popular surgical treatment option for patients suffering from certain SI joint disorders (Rudolf 2012; Duhon et al. 2013; Sachs and Capobianco 2013; Graham Smith et al. 2013). Sacroiliac joint fusion investigation (SIFI, NCT01640353) is a prospective, multicenter single-arm clinical trial of MIS SI joint fusion using triangular-shaped titanium implants (iFuse Implant System ® , SI-BONE, Inc., San Jose, CA, USA) in patients with SI joint disruption and/or degenerative sacroiliitis. The purpose of the present study is to assess the safety and effectiveness of MIS SI joint fusion in a subgroup of patients with degenerative sacroiliitis and/or SI joint disruptions whose pain began in the peri-partum period.
A medical history, neurological exam focused on the lower spine and pelvis, and a series of self-reported questionnaires were obtained at baseline. At postoperative follow-up visits, subjects underwent a neurological exam, adverse event assessment and were required to complete the same self-reported questionnaires. Self-reported questionnaires included SI joint and low back pain as measured on a visual analog scale (VAS), disability due to back pain using the Oswestry Disability Index (ODI), and quality of life using both EuroQol-5D (EQ-5D) and the Short Form-36 (SF-36). VAS was captured on a 0–100 mm unmarked scale with 0 representing no pain and 100 representing the worst pain imaginable. ODI is a validated ten-question survey for disability due to back pain. EQ-5D is a 5-question broad quality of life measure that can be combined into a single that represents the time trade-off (TTO) utility of current health (EuroQol Group 1990). SF-36 is a 36-question 8-subscaled generic quality of life measure that produces both a summary physical component score (PCS) and summary mental component score (MCS) (Ware and Sherbourne 1992). These measures are scaled such that the population norm is approximately 50 with a standard deviation of 10. Female subjects were classified as PPGP if they indicated that their pain began in the peripartum period. In the context of diagnosed SI joint pain, it is assumed that these women have pregnancy-related disruption or degeneration of the SI joint.
Postoperatively, subjects were asked to remain at heel-toe touch-down weight-bearing using a front-wheeled walker or crutches for 3 weeks followed by progressive ambulation with crutches until fully ambulatory. Beginning 1–3 weeks postoperatively, subjects were asked to undergo individualized physical therapy twice a week for 6 weeks. Physical therapy involved activity modification to minimize pain recurrence, mobility and stability exercises, and adjacent segment joint mobilization for stiffness and pain control. Manipulation of the treated SI joint was discouraged.
The study’s primary endpoint was a binary success/failure composite endpoint at 6 months post-operatively. Success was defined if all of the following criteria were met: reduction in VAS SI joint pain by at least 20 mm, and absence of (1) serious device related adverse events, (2) neurological adverse events related to the study device, and (3) re-operation for any reason. Secondary outcome measures included change from baseline on VAS, ODI, EQ-5D, and SF-36 scores (individual components and PCS/MCS) at post-operative time points. Study follow-up will continue out to 2 years.
An exact binomial confidence limit for the 6-month success proportion was calculated and compared with an estimate of the success rate with no treatment in this patient population, estimated at 35 %. A repeated measures analysis of variance was used to evaluate changes from baseline in pain, ODI, EQ-5D and SF-36. Logistic regression was used to compare the success rate in the PPGP group to both women without PPGP and men. Adverse event rates were tabulated. The number of adverse events per subject was compared with Poisson regression. All statistical analyses were performed using R (R Core Team 2013).
SIFI enrolled subject demographics
PPGP (n = 20) mean (SD)
No PPGP (n = 100)
Men (n = 52)
p = 0.002
p = 0.88*
Pain duration (years)
p = 0.62*
Prior lumbar fusion (%)
6 (30 %)
38 (42.2 %)
32 (51.6 %)
p = 0.21†
Prior treatments (n, %)
13 (65 %)
60 (66.7 %)
38 (61.3 %)
p = 0.79†
2 (10 %)
13 (14.4 %)
12 (19.4 %)
p = 0.05†
20 (100 %)
87 (96.7 %)
55 (88.7 %)
p = 0.06†
Target joint, n (%)
83 (48.3 %)
89 (51.7 %)
Procedure time, min
Mean (SD, range)
Fluoroscopy time, min
Mean (SD, range)
Estimated blood loss, cc
Mean (SD, range)
Hospital length of stay, days
Mean (SD, range)
0.8 (0.97, 0–7)
Discharged same day
69 (40.1 %)
85 (49.4 %)
10 (5.8 %)
3 or more
8 (4.7 %)
Patient reported outcomes
Success at 6 months
18 (94.7 %)
78 (78.0 %)
40 (80.0 %)
Success at 12 months
13 (76.5 %)
74 (77.9 %)
38 (82.6 %)
VAS SI pain
12 month change
>20 mm decrease
Change from baseline (p = .3708)§
p < .0001*
p < .0001
p < .0001
12 month change
Change from baseline (p = .3100)
p < .0001
p < .0001
p < .0001
12 month change
Change from baseline (p = .3623)
p < .0001
p < .0001
p < .0001
12 month change
Change from baseline (p = .1313)
p < .0001
p < .0001
p < .0001
12 month change
Change from baseline (p = .0446)
p < .0001
p < .0001
p < .0001
Satisfaction at 12 months (p = .1252)
Very or somewhat satisfied
Would have surgery again (p = .6503)
Might or definitely yes
Adverse events at 12-months
Total number of events
Event rate per subject, mean (SD)
Related to device/procedure
SI joint pain
Numbness around surgical wound
Neuropathy after contralateral SI joint fusion revision
Fall causing SI joint pain. Poor device placement
Roughly 20 % of women who experience back pain during pregnancy report persistent pain 2 and 3 years postpartum (Norén et al. 2002). A substantial proportion of pregnancy- and post-partum-related back pain originates in and around the SI joint. The SI joint is a highly innervated diarthroidal joint subject to high mechanical stresses, especially during the peripartum period. Its exact innervation is quite variable both within and between individuals. In general, innervation of the SI joint is provided by various branches emanating anywhere from L5-S4 (Vleeming et al. 2012; Dreyfuss et al. 2003). These same segments also innervate muscles of the buttocks, hips and lower limbs. Furthermore, pain neurotransmitters, substance P, and calcitonin gene-related polypeptide have been detected in the cartilage of both sides of the joint as well as in the surrounding ligaments (Vleeming et al. 2012). Multisite injections of the sacral nerve roots can block some, but not all, elicited SI joint pain (Dreyfuss et al. 2009). Clearly, there is a neuropathway for pain perception in the region of the SI joint as well as low back, buttock and groin.
SI joint disorders associated with pregnancy are likely multifactorial and can be caused by a combination of hormonal, biomechanical, traumatic and degenerative factors. The design of the pelvic girdle provides the human body with both the stability needed to support the weight of the axial skeleton and the mobility required to accommodate habitual bipedal locomotion and childbirth. The sacrum has been described as “floating” in the pelvic girdle, stabilized by an intricate web of strong ligaments. The unique shape of the auricular surfaces, characterized by complimentary billowing and pitting, along with the basket weave of ligaments, creates self-bracing of the joint, referred to as form closure (Vleeming et al. 1992). Force closure, characterized by muscle forces and ligament tension, is maintained through a myofascial network spanning from the torso to the lower extremities. A small degree of mobility is observed via nutation and counternutation of the sacrum and vertical translation and compression of the pubic symphysis (Becker et al. 2010). Ligament loosening as a result of increased relaxin during pregnancy can create a cascade of events that can lead to degeneration or disruption of the SI joint. Ligaments are viscoelastic structures that creep and deform under constant load. Asymmetric ligament laxity will affect load transfer patterns, causing an imbalance in forces (Aldabe et al. 2012). Additionally, pain in the SI joint can lead to inefficient muscle recruitment, preventing necessary force closure of the joint to maintain stability (Agarwal et al. 2014).
Musculoskeletal structures are inherently unstable, allowing for agility critical to survival. The risk–benefit ratio is precariously held in balance—repeated assaults to the stability mechanism can have long-term degenerative effects (Gracovetsky 2007). A woman’s center of gravity shifts anteriorly both during pregnancy and post-partum while breast feeding, front baby carrying, and as a result of lifting, bending and lowering forces encountered during daily activities of caring for an infant. The constant shift in the center of gravity may result in an anterior rotation of the innominates, potentially leading to a loosening of the force couple, a decrease in intraarticular friction, and possible disruption or subsequent accelerated degeneration of the SI joint (DonTigny 2007).
Few effective non-surgical options are available for women with chronic, persistent PPGP related to the SI joint (Vleeming et al. 2008). The largest body of available literature describes outcomes after physical therapy (PT) interventions. Dysfunction of load transfer in the pelvis as well as delayed onset of muscle activation has been well described as a possible explanation of PGP (Mens et al. 2001; Hungerford et al. 2003; Snijders et al. 1993). This suggests that improvement in muscle activation and strength can alleviate pain. The current literature describes conflicting results. Four studies examined the effect of an intervention consisting of specific muscle stabilizing exercises. One randomized study found that while active care consisting of stabilizing exercises, a pelvic belt and education appears to be effective in alleviating pain during pregnancy (Elden 2005), these same interventions did not prevent post-partum PGP (Elden 2005; Elden et al. 2008). In another randomized trial comparing a program of various specific training exercises to no exercise, no difference was found between groups. Furthermore, while 64 % improved regardless of intervention, 36 % either had no change in symptoms or felt worse after the treatment (Mens et al. 2001). One study found a 20-week program of specific stabilizing exercises to be effective and durable at relieving pain out to 2-years postpartum (Stuge et al. 2004). However, a more recent study reported an individualized exercise program to be ineffective at relieving pain and back-related disability in women with persistent postpartum pelvic girdle pain, with or without concomitant low back pain (Gutke et al. 2010). Thus the literature on physical therapy for PGP and PPGP conveys not only an unclear message about specific stabilizing exercises, but unclear guidance as to which exercises produced favorable results. It is clear that some women may benefit from this approach, but many will have continued pain and degradation in quality of life.
Controlled randomized trials of SI joint injections, both periarticular (methylprednisolone vs. sodium chloride) (Luukkainen et al. 2002), and intra-articular (cartivazol vs. saline) (Maugars et al. 1996) show modest initial improvement in symptoms followed by a quick, marked decline towards baseline levels by 6 months. Similarly, both case series and sham-controlled trials of RF denervation report temporary improvement in less than half of subjects; success rates range from 36 to 47 % (Ferrante et al. 2001; Gevargez et al. 2002; Patel et al. 2012). None of these trials specifically enrolled women with PPGP as the cause of SI joint pain.
Surgical arthrodesis in the spinal column is a common and accepted treatment in the presence of pathology recalcitrant to conservative treatment modalities. Arthrodesis is the process of permanently joining 2 (or more) motion segments in order to eliminate pain caused by motion or abnormal loading of the joint. Success appears to largely depend on clear surgical indications and presence/absence of concomitant pathology and/or psychosocial factors (Spoor and Öner 2013). Pseudoarthrosis, or failure to achieve permanent stabilization, is a well-documented cause of persistent pain postoperatively (Raizman et al. 2009). In a similar vein, fusion of the SI joint has been attempted. The first published report of SI joint fusion through a lateral approach was reported in 1921 (Smith-Petersen 1921). Since that time, the body of literature on open SI joint fusion has grown modestly and documents varying degrees of clinical effectiveness. Compared to more recent reports of minimally invasive approaches, open surgical techniques are associated with relatively long operative times, lengthy hospital stays, considerable soft tissue dissection, and non-weight bearing for long periods of time (3 months). For these reasons, open surgery of the SI joint is usually reserved for the most severe and complicated cases.
Several implants using a variety of MIS techniques are currently available for MIS SI joint fusion. SIFI is a prospective multicenter clinical trial of one such device (iFuse Implant System). A reasonably sized subgroup of patients in this study (17 % of women) reported pain onset in the peripartum period. These women showed improvements in pain, disability and quality of life after MIS SIJ fusion that were similar to both women without PPGP and men. Improvements in pain were clinically significant; 94.7 % achieved pre-defined success in pain improvement and the overall mean improvement was three times larger than that considered to be clinically meaningful (20-point improvement) (Copay et al. 2008). Similarly, improvements in function and quality of life were substantial, exceeding commonly acceptable values. The rate of adverse events in women with PPGP was reasonably low.
The study reported herein has limitations. First, SIFI was not designed to diagnose PPGP. Some women who reported pain onset during pregnancy could have SI joint degeneration related to both peripartum disruption of the joint as well as subsequent joint degeneration as a result of age-related osteoarthritis or other factors such as adjacent segment degeneration after lumbar fusion (Weil et al. 2008). No longitudinal studies have investigated the long-term effects of peripartum SI joint disruption, but it is reasonable to assume that a large portion of affected patients will experience sequelae. Second, the number of subjects with PPGP was fairly low, limiting the ability to draw precise conclusions regarding differences in pain and QOL responses compared to the other subgroups. Nonetheless, no marked differences in pain relief and QOL improvement were seen across groups. Third, the study lacked a concomitant control group of women who received only non-surgical treatment. It is noted that all study participants had chronic (>6 months), carefully diagnosed SI joint pain and many had failed conservative treatment (medications, physical therapy, and, in some cases, RF ablation). Moreover, the mean duration of SI joint pain in PPGP subject was 6.3 years, suggesting both that treatments to date had not adequately relieved pain and that spontaneous pain relief with continued non-surgical treatment would have been unlikely. The findings reported herein are encouraging and represent the first report of minimally invasive surgical treatment for unremitting pain caused by SI joint dysfunction due to disruption or degeneration and associated with pregnancy. Physicians are encouraged to investigate the sacroiliac joint as a potential pain generator in patients presenting with persistent pelvic girdle pain. Moreover, further studies of minimally invasive SI joint fusion for the relief of post-partum-related SI joint pain are warranted.
The sacroiliac joint is a source of pain in approximately 75 % of women with persistent PPGP. Physical therapy, the current mainstay of treatment, is an inconsistent therapeutic option that may provide relief for some women and has been shown to exacerbate symptoms in others. For carefully selected women with chronic post-partum related SI joint dysfunction recalcitrant to conservative therapies, MIS SI joint fusion may be a surgical option that has been shown to provide improvement in pain, disability and quality of life.
RC drafted the manuscript. DC designed the study protocol, edited the manuscript and performed statistical analysis. Both authors read and approved the final manuscript.
We acknowledge the participation of the following SIFI investigators and coordinators: Harry Lockstadt MD, Elaine Wilhite MS, James Farris, PA-C (Bluegrass Orthopaedics and Hand Care, Lexington, KY); Don Kovalsky MD, Laura Pestka RN (Orthopaedic Center of Southern Illinois, Mount Vernon, IL); Cheng Tao MD, Jackie Makowski (Spine and Neuro Center, Huntsville, AL); S. Craig Meyer MD, Vicki Jones (Columbia Orthopaedic Group, Columbia, MO); Scott Kutz MD, Linda Thompson RN BSN, Bradley Gillespie RN, FNP (Mercy Medical Research Center, Springfield, MO); Dimitriy Kondrashov MD, Irina Kondrashov (St. Mary’s Spine, San Francisco, CA); Andy J. Redmond MD, Jennifer Piazza MS (Precision Spine Care, Tyler, TX); CL Soo MD, Kallena Haynes, Antwanya Shaw (Health Research Institute, Oklahoma City, OK); Bradley Duhon MD, Amber Pfister CRC (Neurosurgical and Spine Specialists, Parker, CO); Ali Mesiwala MD, Stephanie Bose RN MSN (Southern California Center for Neuroscience and Spine, Pomona, CA); Leonard Rudolf MD, John Thibodeau Jr RN (Alice Peck Day Memorial Hospital, Lebanon, NH); Kevin Stevenson MD, Logan Honeycutt LPN (Piedmont Orthopaedic Complex, Macon, GA); Fabien Bitan MD, Timolin Jeffers (Manhattan Orthopaedics, New York City, NY); John Stevenson MD, Ana Marichal, (The Orthopaedic Institute, Gainesville, FL); Donald Sachs MD (Center for Spinal Stenosis and Neurological Care, Lakeland, FL); Abhineet Chowdhary MD, Tina Fortney RN BSN (Overlake Hospital Medical Center, Bellevue, WA); Gowriharan Thaiyananthan MD, Tungie Williams (BASIC Spine, Orange, CA); Michael Oh MD, Gary Schmidt MD, Matthew Yeager (Allegheny General Hospital, Pittsburgh, PA); David Wiles MD, Susan Maye RN, MS (East Tennessee Brain & Spine, Johnson City, TN); Michael Hasz MD, Carrie Califano, Anne Copay, PhD (Virginia Spine Institute, Reston, VA); William Rosenberg MD, Amy Akins RN BSN CCRC, Laura Textor, APRN (Midwest Division-RMC, LLC,-Research Medical Center, Kansas City, MO); Jeffrey D. Coe MD, Julia Coe (Silicon Valley Spine, Campbell, CA); Jed Vanichkachorn MD, Jessica Lynch (Tuckahoe Orthopaedics Associates, Richmond, VA); Mark C. Gillespy MD, Sherri Zicker RN (Orthopaedic Clinic of Daytona Beach, Daytona Beach, FL); Ralph Rashbaum MD, Shannon Rusch BA CCRC (Texas Back Institute, Plano, TX); John A. Glaser MD, Emily A. Darr MD, Jennifer Philp (Medical University of South Carolina, Charleston, SC).
SI-BONE sponsored the prospective clinical trial that provided data on SI joint patients described herein. Robyn Capobianco and Daniel Cher are employees of SI-BONE, Inc.
Compliance with ethical guidelines
Competing interests Both authors are employees of SI-BONE, Inc. SI-BONE manufactures the implant used and sponsored the clinical trial reported herein.
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