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Surgical Versus Non-Surgical Treatment for Vertebral Compression Fracture with Osteopenia: A Systematic Review and Meta-Analysis

  • Jia-Bao Guo ,

    Contributed equally to this work with: Jia-Bao Guo, Yi Zhu

    Affiliation Second School of Clinical Medical, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China

  • Yi Zhu ,

    Contributed equally to this work with: Jia-Bao Guo, Yi Zhu

    Affiliation Second School of Clinical Medical, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China

  • Bing-Lin Chen,

    Affiliation Department of sport Rehabilitation, Shanghai University of Sport, Shanghai, China

  • Bin Xie,

    Affiliation Second School of Clinical Medical, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China

  • Wen-Yi Zhang,

    Affiliation Second School of Clinical Medical, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China

  • Yu-Jie Yang,

    Affiliation Second School of Clinical Medical, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China

  • Yu-Shan Yue,

    Affiliation Second School of Clinical Medical, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China

  • Xue-Qiang Wang

    qiang897@163.com

    Affiliation Department of sport Rehabilitation, Shanghai University of Sport, Shanghai, China

Abstract

Background

Surgical and non-surgical interventions are the two categories for treatment of vertebral compression fractures (VCFs). However, there is clinical uncertainty over optimal management. This study aimed to examine the safety and effectiveness of surgical management for treatment of VCFs with osteopenia compared with non-surgical treatment.

Methods

We conducted a systematic search through electronic databases from inception to June 2014, with no limits on study data or language. Randomized controlled trials (RCTs) evaluating surgical versus non-surgical interventions for treatment of patients with VCFs due to osteopenia were considered. Primary outcomes were pain and adverse effects. A random-effects model was used to calculate the pooled mean difference (MD) or risk ratios with 95% confidence interval (CI).

Results

Sixteen reports (11 studies) met the inclusion criteria, and provided data for the meta-analysis with a total of 1,401 participants. Compared with conservative treatment, surgical treatment was more effective in reducing pain (short-term: MD -2.05, 95% CI -3.55 to -0.56, P=0.007; mid-term: MD -1.70, 95% CI -2.78 to -0.62, P=0.002; long-term: MD -1.24, 95% CI -2.20 to -0.29, P=0.01) and disability on the Roland–Morris Disability score (short-term: MD -4.97, 95% CI -8.71 to -1.23, P=0.009), as well as improving quality of life on the Short-Form 36 Physical Component Summary score (short-term: MD 5.53, 95% CI 1.45 to 9.61, P=0.008) and the Quality of Life Questionnaire of the European Foundation for Osteoporosis score (short-term: MD -5.01, 95% CI -8.11 to -1.91, P=0.002). Indirect comparisons between vertebroplasty and kyphoplasty found no evidence that the treatment effect differed across the two interventions for any outcomes assessed. Compared with the sham procedure, surgical treatment showed no evidence of improvement in pain relief and physical function. Based on these two comparisons, no significant difference between groups was noted in the pooled results for adverse events.

Conclusion

Compared to conservative treatment, surgical treatment was more effective in decreasing pain in the short,mid and long terms. However, no significant mid- and long-term differences in physical function and quality of life was observed. Little good evidence is available for surgical treatment compared with that for sham procedure. PV and BK are currently used to treat VCFs with osteopenia, with little difference in treatment effects. Evidence of better quality and from a larger sample size is required before a recommendation can be made.

Systematic Review Registration

http://www.crd.york.ac.uk/PROSPERO PROSPERO registration number: CRD42013005142.

Introduction

An estimated 1.4 million vertebral compression fractures (VCFs) are reported worldwide every year [1]. Patients with VCF may present with severe back pain, functional disability, and a decrease in quality of life [2, 3]. The most common etiology of VCFs is osteoporosis, although trauma, infection, and tumour can also lead to VCFs. Bone metastases and multiple myeloma can lead to generalised osteoporosis or weakening of bone at specific sites [4]. As a result, fractures were caused, especially painful VCFs. Aging is associated with a decrease in bone mineral density [57]. VCFs secondary to osteopenia arising from osteoporosis, fall or tumours are a cause of morbidity in older adults. These fractures will increase with the increasing aging of the population [8, 9].

Surgical and non-surgical methods are used to treat VCFs. Standard non-surgical treatment includes bed rest, analgesia, use of a back brace or corset, and physical support. Minimally invasive techniques, such as percutaneous vertebroplasty (PV) and balloon kyphoplasty (BK), are popular for treating painful VCFs [1013]. PV involves the percutaneous injection of bone cement into the affected vertebra to stabilize the fractured vertebral body, and results in immediate pain relief. It was initially devised in France by Deramond and Galibert in 1984, and first performed to treat hemangioma in the cervical spine [14, 15]. Since then, the operation has become widely used and proved valuable in treating osteoporotic VCFs. BK is a type of PV in which inflatable bone tamps are used to restore vertebral height. After removing the balloons, the resulting intravertebral cavity is filled with bone cement to stabilize the vertebral body. No consensus has been reached over which is the best management strategy for patients with VCFs.

Several published systematic reviews have assessed the effects of surgical management for the treatment of VCFs [1619]. However, previous reviews focused on one type of surgical management, such as PV or BK. To synthesise the latest trial reports, we have performed this systematic review and meta-analysis of randomized controlled trials (RCTs) of surgical management for treatment of VCFs with osteopenia compared with non-surgical treatment. This review includes trials evaluating a variety of different surgical methods as used to treat people with VCFs due to osteopenia, which provide an overall assessment on the use of surgical managements in this patients population. To our best knowledge, this study is the first comprehensive meta-analysis of surgical management versus non-surgical management in this issue.

Methods

Search Strategy

We did a systematic review in accordance with the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) guidelines [20]. For a completed PRISMA checklist, see S1 Checklist. The Cochrane Central Register of Controlled Trials, PubMed, EMBASE, Web of Science, China Biology Medicine disc, China National Knowledge Infrastructure, and Wanfang Database were searched from the earliest available date to June 2014. We used “Vertebroplasty”, “Fractures, Bone” and “RCTs” as search terms (full details of the search in S1 File). Reference lists of selected articles were reviewed for other potentially relevant citations.

Inclusion Criteria

Types of studies.

Only RCTs investigating surgical versus non-surgical interventions for the treatment of patients with VCFs were included. No limits on publication dates or any language restrictions were placed.

Types of participants.

Patients with VCFs due to osteopenia arising from osteoporosis or tumours were included. We excluded patients who had severe cardiopulmonary comorbidity, untreatable coagulopathy, systemic or local spine infection, suspected underlying malignant disease, radicular syndrome, spinal cord compression syndrome, or contraindications to magnetic resonance imaging.

Types of interventions.

We included an experimental group that received surgical treatment, and a control condition in which either conservative treatment or a sham procedure was administered. Surgical treatments included vertebroplasty, kyphoplasty, pedicle screw fixation, anterior reconstruction or fusion, and posterior reconstruction or fusion. Patients in the sham surgical intervention group underwent the same procedure as those in the experimental group up to the insertion of the needle. Conservative interventions consisted of bed rest, medication (e.g., analgesics), use of a corset, brace, or cast, and rehabilitation (e.g., physiotherapy).

Types of outcome measures.

The primary outcomes were self-reported pain and adverse effects. All reported symptomatic and asymptomatic adverse events were recorded. Secondary outcomes were function or disability, health-related quality of life, and hospitalization costs. The costs included procedural costs, rehabilitation costs, and primary costs. All outcome measures were pre-specified before review commencement. We categorized outcomes as short-term (not longer than three months), mid-term (six months), and long-term (twelve months or more) follow-up. All outcome measures were pre-specified before review commencement.

Data Extraction

Two reviewers (Guo JB and Xie B) independently extracted and cross-checked data on trials. The decision to include studies was made initially on the basis of the study title and abstract. When a study could not be excluded with certainty at this stage, the full-text was obtained for evaluation. Disagreements were resolved by discussion and, where necessary, in consultation with a third reviewer (Zhang WY). Extracted information included the first author, publication year, study design (e.g., intervention, follow-up length, outcome measures), characteristics of participants (e.g., age, gender, inclusion/exclusion criteria, sample size, duration of complaint), and information to assess the risk of bias.

Quality Assessment

The risk of bias of the included studies was independently assessed by two authors (Guo JB and Chen BL) using the Cochrane Collaboration’s “Risk of Bias” [21]. We assessed the following domains: sequence generation, allocation concealment, blinding of participants and personnel, blinding of outcome assessment, incomplete outcome data, selective outcome reporting, and other sources of bias. Risk of bias was categorized as low, unclear, or high for each of the included studies. Disagreements were resolved by third party adjudication.

Statistical Analysis

Quantitative data were entered into Review Manager (RevMan 5.1). When appropriate, results of comparable groups of studies were pooled in a meta-analysis using the random-effects model. For dichotomous outcomes, risk ratios (RRs) with 95% confidence intervals (CIs) were calculated. For continuous outcomes, mean difference (MDs) with 95% CIs or standardized mean differences with 95% CI were calculated. P values were 2-tailed, and a value of P<0.05 was considered statistically significant. Heterogeneity between studies was measured by Chi2 statistic (P<0.1) and quantified with I² statistic [22]. We judged the I2 values of less than 25% to be minimal heterogeneity, less than50% to be moderate heterogeneity, and 50% or greater to be substantial heterogeneity. In attempting to dissipate any heterogeneity, subgroup analyses were performed on studies. Since the different trials implemented various types of surgical management, trials were divided according to the type of intervention (e.g., PV, BK). If there were two or more surgical methods in the same comparison, then the subgroup analysis was conducted. Potential publication bias was evaluated using funnel plots.

When studies required for the meta-analysis did not provide means and standard deviations at follow-up, we contacted corresponding authors to obtain the unreported data. In the few cases in which a response was unavailable, we estimated the standard deviations using the formula suggested in the Cochrane Handbook for Systematic Reviews of Interventions [23].

Results

Our search identified a total of 10,374 records. After removing duplicates, 6,251 records were screened. A further 74 were determined to be potentially relevant for full-text review. Among these studies, 11 studies (16 reports) met the inclusion criteria [2439], and provided data for the meta-analysis. A manual search of reference lists from these studies did not yield any new eligible study (Fig 1).

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Fig 1. Flow chart of study selection.

For details of study identification.

https://doi.org/10.1371/journal.pone.0127145.g001

Study characteristics

Eleven studies (16 reports) were included, and a summary of their characteristics is shown in Table 1. Six studies [27, 29, 3436, 38, 39] were small single-center trials, and five [24, 25, 27, 28, 3033, 37] were multicenter trials. All the studies used surgical treatment as the intervention. Two types of interventions were used; eight studies [2426, 3035, 38, 39] used PV, three studies [2729, 36, 37] used BK. Regarding controls, ten studies [2629, 3139] used conservative treatment and two [24, 25, 30] used sham surgical treatment. All participants had VCFs due to osteopenia. One study [37] arised from bone metastases and multiple myeloma. Another study [27] was caused by either osteoporosis or tumours, and the other participants all had osteoporotic VCFs. Data from 1,401 participants were extracted, of whom 701 received surgical treatment.

Qualitative Assessment

Methodological details are reported in S1 and S2 Figs. Three (18.75%) trials [31, 2737, 39] were not provided with allocation concealment, which resulted in unclear risk of selection bias. Thirteen (81.25%) trials [2629, 3139] were at high risk of performance bias, reflecting the difficulty in blinding surgeons. Only one (6.25%) trial [36] did not describe the patients who withdrew from the study. Finally, 11 (68.75%) trials [24, 25, 2730, 3233, 3739] stated per protocol the primary method of analysis, and the remaining trials did not describe the method of analysis.

Comparison 1: Surgical Versus Conservative Interventions for Treating VCF with Osteopenia

Self-related pain

In total, ten trials evaluated self-related pain using a numeric rating scale (NRS) and a visual analog scale (VAS). Among these trials, nine (1,014 patients) reported data at short-term follow-up period, four (597 patients) at mid-term follow-up period and five (604 patients) at long-term follow-up term. We found significant improvements with surgical management for pain relief in the short term (MD −2.05, 95% CI, −3.55 to −0.56; P = 0.007), mid term (MD −1.70, 95% CI, −2.78 to −0.62; P = 0.002) and long term (MD −1.24, 95% CI, −2.20 to −0.29; P = 0.01) (Fig 2). In the test for subgroup differences, PV was seen to be more effective than conservative treatment at short-term (MD −1.28, 95% CI, −2.42 to −0.13; P = 0.03) (Fig 2A), mid-term (MD −1.79, 95% CI, −3.38 to −0.20; P = 0.03) (Fig 2B), and long-term follow-up periods (MD −1.38, 95% CI, −2.64 to −0.12; P = 0.03) (Fig 2C) in reducing pain. We only found significant improvements with BK for pain relief in the short term (MD −3.60, 95% CI, −5.80 to −1.39; P = 0.001) (Fig 2A). In addition, it can be observed that the funnel plot had an asymmetrical distribution regarding self-related pain at short-term follow-up period (Fig 3). There was a suggestion of publication bias according to the shape of the funnel plot.

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Fig 2. Self-related pain for surgical versus conservative treatment.

A: mean difference (MD) at the end of the intervention (not longer than 3 months). B: MD at six months. C: MD at long-term follow-up period (12 months or more). PV, percutaneous vertebroplasty; BK, balloon kyphoplasty; CI, confidence interval; IV, inverse variance.

https://doi.org/10.1371/journal.pone.0127145.g002

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Fig 3. Funnel plot of included studies regarding self-related pain in the short term.

Short term: not longer than 3 months. Log of mean difference were plotted against the standard error of mean difference of each study to identify asymmetry in the distribution of trials.

https://doi.org/10.1371/journal.pone.0127145.g003

Adverse events

Overall, no significant difference between surgical and conservative treatments was observed for adverse events from seven trials consisting of 855 patients (139/433 versus 124/422; RR 1.10, 95% CI, 0.85 to 1.43; P = 0.46) (Fig 4). In the test for subgroup differences, five trials reported no significant difference between PV and conservative treatments(39/214 versus 32/207; RR 1.29, 95% CI, 0.65 to 2.59; P = 0.47), and two reported no significant difference between BK and conservative treatments(100/219 versus 92/215; RR 1.07, 95% CI, 0.86 to 1.31; P = 0.55). One trial was not entered into this forest plot because of incomplete data. The study did not report adverse events in the control group [38]. Further analyses by types of adverse events showed that musculoskeletal disorders were the most common adverse events in both groups. Among musculoskeletal disorders, the frequency of new fractures was the highest (97/402 versus 80/373), but no statistically significant difference was observed between groups (P = 0.62) (Fig 5).

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Fig 4. Overall adverse events for surgical versus conservative treatment.

Markers represent point estimates of risk ratios, marker size represents study weight in random-effects meta-analysis. Horizontal bars indicate 95% confidence intervals. CI, confidence interval; M-H, mantel-haenszel.

https://doi.org/10.1371/journal.pone.0127145.g004

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Fig 5. Incidence of new fractures for surgical versus conservative treatment.

https://doi.org/10.1371/journal.pone.0127145.g005

For individual adverse events, no statistically significant difference between the surgical and conservative treatment groups was observed (S3 Fig). One study [32] stated that adverse events related to surgical procedure include hematoma and urinary tract infection. Other adverse events that have been reported include infections, cardiovascular and vascular disorders, injury or procedural complications, and blood and lymphatic disorders.

Function or disability

Four trials collected data for the Roland—Morris Disability (RMD) score, with three (372 patients) reporting a decrease in the RMD score after surgical intervention at short-term follow-up period (MD −4.97, 95% CI, −8.71 to −1.23; P = 0.009) (Fig 6). In the test for subgroup differences, RMD score decreased with BK compared with that with conservative treatment (MD -5.99, 95% CI, -10.60 to -1.38; P = 0.01). Only one trial [28] at six months follow-up was noted, and surgical treatment was more effective in disability on the RMD score. However, no significant differences were observed between groups at twenty-four months follow-up.

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Fig 6. RMD score for surgical versus conservative treatment in the short term.

Short term: not longer than 3 months.

https://doi.org/10.1371/journal.pone.0127145.g006

Health-related quality of life

We used more than one measure of quality of life, and we preferentially included the following measures: the Short-Form 36 (SF-36), the Quality of Life Questionnaire of the European Foundation for Osteoporosis (QUALEFFO), and the European Quality of Life–5 Dimensions (EQ-5D).

SF-36: Four trials, with a total of 614 patients reported data for the Short-Form 36 Physical Component Summary (SF-36 PCS) score. We observed a greater increase at short-term follow-up period after surgical procedure (MD 5.53, 95% CI, 1.45 to 9.61; P = 0.008) (Fig 7A). In the test for subgroup differences, we observed significant differences in favor of BK at short-term follow-up period (MD 7.16, 95% CI, 5.72 to 8.60; P < 0.00001). However, no difference was observed between the two groups at long-term follow-up period (MD 1.20, 95% CI, −1.33 to 3.72; P = 0.93) (Fig 7B). A single trial [25] reported that surgical treatment was more effective in improving quality of life on the SF-36 PCS score at six months follow-up. Considering the Short-Form 36 Mental Component Summary (SF-36 MCS) score, only small study effects were found in favor of the surgical group at short-term follow-up period (MD 7.38, 95% CI, 1.13 to 13.63; P = 0.02) (S4 Fig).

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Fig 7. SF-36 PCS score for surgical versus conservative treatment.

A: mean difference (MD) at the end of the intervention (not longer than 3 months). B: MD at long-term follow-up period (12 months or more).

https://doi.org/10.1371/journal.pone.0127145.g007

QUALEFFO: Two trials (144 patients) collected data for the QUALEFFO score, which reported that surgical treatment was more effective than conservative treatment at short-term follow-up period (MD −5.01, 95% CI, −8.11 to −1.91; P = 0.002) (S5 Fig). A single trial [39] reported that significant improvement was obtained at both six and twelve months follow-up in the surgical group.

EQ-5D: Three trials, with a total of 500 patients reported data for EQ-5D. However, no significant differences were observed between surgical and conservative management for the EQ-5D score at short- or long-term follow-up periods. (S6 Fig).

Hospitalization costs

Two trials [29, 32] reported hospitalization costs. Data from Klazen [32] showed that the cost of surgery in the first month was higher than the cost of conservative treatment because of procedural costs (P < 0.0001). However, the difference was no longer significant at one year (P = 0.087), which resulted from continued pain and loss of function in the conservative treatment group. The resulting incremental cost-effectiveness suggested that vertebroplasty was warranted for the patients with vertebral fractures treated at a mean of 5.6 weeks after the start of symptoms. Data from Fritzell [29] demonstrated that BK costs more than standard medical treatment with a significant difference of 7,833€(95% CI, 1671 to 12,511), and from this trial it was not possible to demonstrate that BK was more cost-effective than standard medical treatment in patients treated for an acute or subacute vertebral fracture because of osteoporosis.

Comparison 2: Surgical Intervention Versus a sham Surgical Procedure for Treating VCF with Osteopenia

Self-related pain

Three trials collected data for self-related pain, with two (198 patients) reporting pain relief after surgical intervention at short-term follow-up period (MD −4.97, 95% CI, −8.71 to −1.23; P = 0.009) (Fig 8). However, no significant differences were found in the mid term. Only one trial [30] at twelve months follow-up period was noted, and there were no significant differences between two groups. Only one surgical method PV was used, so we did not make any subgroup analyses in comparison 2.

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Fig 8. Self-related pain for surgical versus sham surgical treatment.

Short term: not longer than 3 months; Mid term: 6 months.

https://doi.org/10.1371/journal.pone.0127145.g008

Adverse events

Data on adverse events were available for both studies. No significant difference between surgical intervention and sham surgical intervention was observed in the pooled results for overall adverse events (20/106 versus 16/103; RR 1.32, 95% CI, 0.80 to 2.18; P = 0.28) (S7 Fig). Adverse events in the two studies included incident fracture, injury or procedural complications, tachycardia and rigors, osteomyelitis, tightness in the back or rib cage, and pain [24,25].

Function or disability

Three trials collected data for the RMD score, and no significant difference was found among groups at short-term (MD 0.03, 95% CI, −1.77 to 1.83; P = 0.98) and mid-term follow-up periods (MD −0.73, 95% CI, −2.76 to 1.30; P = 0.48 (S8 Fig). A single trial [30] reported that there were no significant differences between groups at twelve months follow-up.

Health-related quality of life

A single trial [25] found no significant difference between the two intervention groups at one month follow-up for the SF-36 PCS score, SF-36 MCS score, and EQ-5D score. Considering the QUALEFFO score, no significant differences were observed between groups at any time points measured, except at one week, which favored the sham procedure group [24].

Subgroup analysis

The primary comparison in this review was any surgical intervention versus any conservative intervention. Secondary comparison analyses were any surgical intervention versus a sham surgical procedure. The subgroup analysis included two comparisons as follows: PV versus conservative treatment and BK versus conservative treatment. Only one outcome, the self-related pain at short-term follow-up period, showed significant heterogeneity between the treatment effects of the different classes of intervention. In all other cases, threre was no significant heterogeneity between the treatment effects of the different classes of intervention (Table 2). One outlying trial was the cause of this heterogeneity in the self-related pain at short-term follow-up period [37]; when this trial was excluded from the analysis, the result remained significant (MD −1.85, 95% CI, −3.68 to −0.02; P = 0.05), but the test for between subgroup heterogeneity was no longer significant (P = 0.30).

Discussion

Previous reviews have examined the results of PV versus conservative treatment or BK versus conservative treatment, but none has combined the surgical methods. BK is a type of PV, and they invovle similar techniques. In addition, both of them have less invasive procedures with similar risk profiles compared to open surgery. Therefore, this review collated all the evidence from a large number of trials, which evaluated vertebroplasty and kyphoplasty into one review to assess the overall effect of surgical versus non-surgical treatment of VCFs with osteopenia. It also allowed an indirect comparison of between PV and BK, and provided no evidence of differences in the treatment effect between the two types of surgical methods.

Statistical significance was reported in comparison one for five outcomes: self-related pain, RMD, SF-36 PCS, SF-36 MCS, and QUALEFFO. The most of the significant differences we observed were at short-term follow-up period. Only the improvements of self-related pain were seen in the short, mid, and long terms. This meta-analysis suggested a favorable association of surgical treatment in reducing pain, improving function and quality of life compared with conservative treatment. By contrast, when we focused on the two studies [24, 25] in which surgical procedure was compared with sham procedure, we saw no evidence of improvement in pain relief, physical function and quality of life. The kind of these two studies is generally speaking difficult to achieve in surgical procedures, and often reaches the limit of ethically acceptable studies. Both studies are multicenter, double-blind RCTs published in the New England Journal of Medicine. The results from the two papers have aroused worldwide attention and intense controversy [4042]. The placebo effect may be explained by several reasons, such as narcotic effects, psychological effects, and neural excitatory effects. However, at long-term follow-up period, pain relief with placebo treatment was similar to that with surgical management. Samuel Butler [40] stated that these two studies comprised samples fewer than 300 patients in both the treatment and control groups, and many patients were unwilling to accept randomization, especially for patients in severe pain. Thus, the small size of sample and selection bias made these studies untrustworthy. In spite of these limitations, we still observed a statistical trend, which suggested that vertebroplasty was more effective than sham treatment. For example, data from Kallmes [25] showed a higher rate of clinically meaningful improvement in pain relief in the vertebroplasty group than that in the control group (64% versus 48%, P = 0.06). Vertebroplasty may be effective with a larger sample size. Therefore, high-quality, well-designed studies are needed to address the areas of uncertainty.

The incidence of new fractures was similar after surgical and conservative therapy. Thus, the occurrence of new vertebral fractures was due to ongoing osteoporosis and not the type of therapy. About 20% of patients with a history of osteoporotic vertebral fractures will experience a new vertebral fracture within a year, depending on the severity of the prior fracture [43]. In addition, no statistically significant difference was observed between groups in other adverse events. In this meta-analysis, we did not believe that the risk of adverse events after surgery should be a contraindication for the operation.

The findings from our review were consistent with findings from previous reviews. Five reviews have been published, and all of them included trials only using vertebroplasty as the experimental group [1619, 44]. Four of these reviews [1617, 19, 44] restricted the results to RCTs only, whereas one [18] included randomized and non-randomized clinical trials. Three of these reviews [16, 17, 19] found that vertebroplasty in pain relief is more obvious than that in conservative treatment at short-term, mid-term, and long-term follow-up. Four trials [16, 17, 19, 44] compared vertebroplasty with a sham procedure in patients with VCFs, and all failed to show an advantage of vertebroplasty over placebo.

Strengths

Our study had several strengths. The review highlights the wide range of surgical techniques being used in the treatment of VCFs with osteopenia, and previous reviews focused on one type of surgical management. We made subgroup analyses for vertebroplasty and kyphoplasty, and it allowed an indirect comparison between them. Our review methods were systematic and exhaustive. We employed a broad search strategy without any publication dates or language restrictions. Relevant citations in selected articles were also examined. All trials included in our review were RCTs. Study selection, quality assessment, and data extraction were performed by at least two independent reviewers. We mapped all possible treatment comparisons, and six outcomes were reported in this meta-analysis. Some heterogeneity was observed in the meta-analysis, so we generated random-effects models that accounted for between-study variability.

Limitations

First, all studies included in this review used pain scales. However, different studies used different pain surveys as outcomes, which possibly created some of the heterogeneity we observed among trials. Second, we noted minimal focus on hospitalization cost analysis of the surgical intervention; therefore, little is known about the cost-effectiveness and economic value of these surgical managements. Third, we estimated the standard deviations for several studies using the formula suggested in the Cochrane Handbook for Systematic Reviews of Interventions because a response was unavailable from certain authors.

Implications for Research

Evidence of better quality and from a larger sample size is required before a recommendation can be made. Further RCTs are needed until we can establish whether surgical management is more effective than non-surgical management in patients with VCFs due to osteopenia. Future studies should identify which type of surgical treatment provides more advantages. The shortcomings of the present evidence in this review include small study size, selection bias, performance bias, detection bias, and attrition bias. Future trials should be reported following the CONSORT guidelines [45], and data should be analyzed according to intention to treat principles. This review illustrated the need for the universal use of relevant outcome measures, especially adverse events and hospitalization cost outcomes. Moreover, systematic data collection at short, mid-, and long-term follow-up is essential.

Supporting Information

S1 Checklist. PRISMA Checklist of this meta-analysis.

https://doi.org/10.1371/journal.pone.0127145.s001

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S1 File. Search strategies for all databases.

https://doi.org/10.1371/journal.pone.0127145.s002

(DOC)

S1 Fig. Risk of bias graph using the Cochrane Risk of Bias tool.

https://doi.org/10.1371/journal.pone.0127145.s003

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S2 Fig. Risk of bias summary using the Cochrane Risk of Bias tool.

https://doi.org/10.1371/journal.pone.0127145.s004

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S3 Fig. Individual adverse events for surgical versus conservative treatment.

Markers represent point estimates of risk ratios, marker size represents study weight in random-effects meta-analysis. Horizontal bars indicate 95% confidence intervals. CI, confidence interval; M-H, mantel-haenszel.

https://doi.org/10.1371/journal.pone.0127145.s005

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S4 Fig. SF-36 MCS score for surgical versus conservative treatment in the short term.

Short term: not longer than 3 months; Markers represent point estimates of mean difference, marker size represents study weight in random-effects meta-analysis. Horizontal bars indicate 95% confidence intervals. CI, confidence interval; IV, inverse variance.

https://doi.org/10.1371/journal.pone.0127145.s006

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S5 Fig. QUALEFFO score for surgical versus conservative treatment in the short term.

Short term: not longer than 3 months; Markers represent point estimates of mean difference, marker size represents study weight in random-effects meta-analysis. Horizontal bars indicate 95% confidence intervals. CI, confidence interval; IV, inverse variance.

https://doi.org/10.1371/journal.pone.0127145.s007

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S6 Fig. EQ-5D score for surgical versus conservative treatment in the short and long terms.

Short term: not longer than 3 months; Long term: 12 months or more; Markers represent point estimates of mean difference, marker size represents study weight in random-effects meta-analysis. Horizontal bars indicate 95% confidence intervals. CI, confidence interval; IV, inverse variance.

https://doi.org/10.1371/journal.pone.0127145.s008

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S7 Fig. Overall adverse events for surgical versus sham surgical treatment.

Markers represent point estimates of risk ratios, marker size represents study weight in random-effects meta-analysis. Horizontal bars indicate 95% confidence intervals. CI, confidence interval; M-H, mantel-haenszel.

https://doi.org/10.1371/journal.pone.0127145.s009

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S8 Fig. RMD score for surgical versus sham surgical treatment in the short and mid terms.

Short term: not longer than 3 months; Mid term: 6 months; Markers represent point estimates of mean difference, marker size represents study weight in random-effects meta-analysis. Horizontal bars indicate 95% confidence intervals. CI, confidence interval; IV, inverse variance.

https://doi.org/10.1371/journal.pone.0127145.s010

(TIF)

Acknowledgments

This work was supported by Key Laboratory of Exercise and Health Sciences of Ministry of Education, Shanghai University of Sport; Innovation Program of Shanghai Municipal Education Commission (15ZZ084); Shanghai Committee of Science and Technology (14490503800); Shanghai Youth Science and Technology Sail Project (15YF1411400).

And we would like to sincerely thank Professor Rui-He Yang, Department of Orthopedics, Changhai Hospital, Shanghai, China, for his clinical practice recommendations.

Author Contributions

Conceived and designed the experiments: X-QW. Performed the experiments: J-BG YZ. Analyzed the data: J-BG B-LC BX W-YZ. Contributed reagents/materials/analysis tools: Y-SY Y-JY. Wrote the paper: X-QW YZ.

References

  1. 1. Johnell O, Kanis JA. An estimate of the worldwide prevalence and disability associated with osteoporotic fractures. Osteoporos Int. 2006; 17: 1726–1733. pmid:16983459
  2. 2. Borgström F, Zethraeus N, Johnell O, Lidgren L, Ponzer S, Svensson O, et al. Costs and quality of life associated with osteoporosis-related fractures in Sweden. Osteoporos Int. 2006; 17: 637–650. pmid:16283064
  3. 3. Silverman SL, Minshall ME, Shen W, Harper KD, Xie S. The relationship of health-related quality of life to prevalent and incident vertebral fractures in postmenopausal women with osteoporosis: results from the Multiple Outcomes of Raloxifene Evaluation Study. Arthritis Rheum. 2001; 44: 2611–2619. pmid:11710717
  4. 4. Coleman RE. Skeletal complications of malignancy. Cancer. 1997; 80 (suppl 8): 1588–1594. pmid:9362426
  5. 5. Li R. Women’s health in exercise and aging: What do we know? Journal of Sport and Health Science. 2014; 3:153–154.
  6. 6. Kendall KL, Fairman CM. Women and exercise in aging. Journal of Sport and Health Science. 2014; 3:170–178.
  7. 7. Connolly LJ, Scott S, Mohr M, Ermidis G, Julian R, Bangsbo J, Jackman SR, et al. Effects of small-volume soccer and vibration training on body composition, aerobic fitness, and muscular PCr kinetics for inactive women aged 20–45. Journal of Sport and Health Science. 2014; 3:284–292.
  8. 8. Green AD, Colón-Emeric CS, Bastian L, Drake MT, Lyles KW. Does this woman have osteoporosis? JAMA. 2004; 292: 2890–2900. pmid:15598921
  9. 9. Paquette MR, Li Yuhua, Hoekstra J, Bravo J. An 8-week reactive balance training program in older healthy adults: A preliminary investigation. Journal of Sport and Health Science. 2014; In press. pmid:25685605
  10. 10. Garfin SR, Yuan HA, Reiley MA. New technologies in spine: kyphoplasty and vertebroplasty for the treatment of painful osteoporotic compression fractures. Spine. 2001; (Phila Pa 1976) 26: 1511–1515. pmid:11462078
  11. 11. McGraw JK, Lippert JA, Minkus KD, Rami PM, Davis TM, Budzik RF. Prospective evaluation of pain relief in 100 patients undergoing percutaneous vertebroplasty: results and follow-up. J Vasc Interv Radiol. 2002; 13: 883–886. pmid:12354821
  12. 12. Garfin SR, Buckley RA, Ledlie J. Balloon Kyphoplasty Outcomes Group: Balloon kyphoplasty for symptomatic vertebral body compression fractures results in rapid, significant, and sustained improvements in back pain, function, and quality of life for elderly patients. Spine. 2006; (Phila Pa 1976) 31: 2213–2220. pmid:16946656
  13. 13. Grafe IA, Da Fonseca K, Hillmeier J, Meeder PJ, Libicher M, Nöldge G, et al. Reduction of pain and fracture incidence after kyphoplasty: 1-year outcomes of a prospective controlled trial of patients with primary osteoporosis. Osteoporos Int. 2005; 16: 2005–2012. pmid:16078092
  14. 14. Galibert P, Deramond H, Rosat P, Le Gars D. [Preliminary note on the treatment of vertebral angioma by percutaneous acrylic vertebroplasty]. Neurochirurgie. 1987; 33: 166–168. pmid:3600949
  15. 15. Deramond H, Wright NT, Belkoff SM. Temperature elevation caused by bone cement polymerization during vertebroplasty. Bone. 1999; 25(2 Suppl): 17S–21S. pmid:10458268
  16. 16. Zh Tian, Tian H, Wang Ch. Percutaneous vertebroplasty versus conservative treatment of osteoporotic vertebral compression fractures: a systematic review. Chin J Osteoporos. 2008; 14: 396–401. pmid:25140056
  17. 17. Xu JC, Bai JP, XiLin BLR, He ZS, Jiang RB, Huang WM. Vertebroplasty injected with bone cement versus non-operative treatment for osteoporotic vertebral compression fractures: a meta-analysis. CRTER. 2011; 15: 2366–2370.
  18. 18. Cao LY, Wang JM, Yang SP, Jing MJ. Vertebroplasty versus non-operative therapy for the treatment of osteoporotic vertebral compressive fractures: a systematic review. Chin J Osteoporos. 2012; 18: 516–522.
  19. 19. Liu J, Li X, Tang D, Cui X, Li X, Yao M, et al. Comparing pain reduction following vertebroplasty and conservative treatment for osteoporotic vertebral compression fractures: a meta-analysis of randomized controlled trials. Pain Physician. 2013; 16: 455–464. pmid:24077192
  20. 20. Moher D, Liberati A, Tetzlaff J, Altman DG, PRISMA Group. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. BMJ. 2009; 339: b2535. pmid:20171303
  21. 21. Higgins JPT, Green S, eds. Cochrane handbook for systematic reviews of interventions. Version 5.1.0. Cochrane Collaboration. 2011.
  22. 22. Higgins JP, Thompson SG, Deeks JJ, Altman DG. Measuring inconsistency in meta-analyses. BMJ. 2003; 327: 557–560. pmid:12958120
  23. 23. Higgins JP, Altman DG, Gøtzsche PC, Jüni P, Moher D, Oxman AD, et al. The Cochrane Collaboration's tool for assessing risk of bias in randomised trials. BMJ. 2011; 343: d5928. pmid:22008217
  24. 24. Buchbinder R, Osborne RH, Ebeling PR, Wark JD, Mitchell P, Wriedt C, et al. A randomized trial of vertebroplasty for painful osteoporotic vertebral fractures. N Engl J Med. 2009; 361: 557–568. pmid:19657121
  25. 25. Kallmes DF, Comstock BA, Heagerty PJ, Turner JA, Wilson DJ, Diamond TH, et al. A randomized trial of vertebroplasty for osteoporotic spinal fractures. N Engl J Med. 2009; 361: 569–579. pmid:19657122
  26. 26. Voormolen MH, Mali WP, Lohle PN, Fransen H, Lampmann LE, van der Graaf Y, et al. Percutaneous vertebroplasty compared with optimal pain medication treatment: short-term clinical outcome of patients with subacute or chronic painful osteoporotic vertebral compression fractures. The VERTOS study. AJNR Am J Neuroradiol. 2007; 28: 555–560. pmid:17353335
  27. 27. Wardlaw D, Cummings SR, Van Meirhaeghe J, Bastian L, Tillman JB, Ranstam J, et al. Efficacy and safety of balloon kyphoplasty compared with non-surgical care for vertebral compression fracture (FREE): a randomised controlled trial. Lancet. 2009; 373: 1016–1024. pmid:19246088
  28. 28. Boonen S, Van Meirhaeghe J, Bastian L, Cummings SR, Ranstam J, Tillman JB, et al. Balloon kyphoplasty for the treatment of acute vertebral compression fractures: 2-year results from a randomized trial. J Bone Miner Res. 2011; 26: 1627–1637. pmid:21337428
  29. 29. Fritzell P, Ohlin A, Borgström F. Cost-effectiveness of balloon kyphoplasty versus standard medical treatment in patients with osteoporotic vertebral compression fracture: a Swedish multicenter randomized controlled trial with 2-year follow-up. Spine (Phila Pa 1976). 2011; 36: 2243–2251. pmid:21912321
  30. 30. Comstock BA, Sitlani CM, Jarvik JG, Heagerty PJ, Turner JA, Kallmes DF. Investigational vertebroplasty safety and efficacy trial (INVEST): patient-reported outcomes through 1 year. Radiology. 2013; 269: 224–231. pmid:23696683
  31. 31. Chen G, Zhang ST, Liu YC, Sun RZ, Zhao X, Luo D. Percutaneous vertebroplasty compared to conservative treatment in patients with osteoporotic vertebral compression fractures. J Cervicodynia Lumbodynia. 2010; 31: 323–326.
  32. 32. Klazen CA, Lohle PN, de Vries J, Jansen FH, Tielbeek AV, Blonk MC, et al. Vertebroplasty versus conservative treatment in acute osteoporotic vertebral compression fractures (Vertos II): an open-label randomised trial. Lancet. 2010; 376: 1085–1092. pmid:20701962
  33. 33. Klazen CA, Venmans A, de Vries J, van Rooij WJ, Jansen FH, Blonk MC, et al. Percutaneous vertebroplasty is not a risk factor for new osteoporotic compression fractures: results from VERTOS II. AJNR Am J Neuroradiol. 2010; 31: 1447–1450. pmid:20651016
  34. 34. Rousing R, Andersen MO, Jespersen SM, Thomsen K, Lauritsen J. Percutaneous vertebroplasty compared to conservative treatment in patients with painful acute or subacute osteoporotic vertebral fractures: three-months follow-up in a clinical randomized study. Spine (Phila Pa 1976). 2009; 34: 1349–1354. pmid:19478654
  35. 35. Rousing R, Hansen KL, Andersen MO, Jespersen SM, Thomsen K, Lauritsen JM. Twelve-months follow-up in forty-nine patients with acute/semiacute osteoporotic vertebral fractures treated conservatively or with percutaneous vertebroplasty: a clinical randomized study. Spine. 2010; 35: 478–482. pmid:20190623
  36. 36. Xie E, Hao DJ, Yang TM, Wu QN. Percutaneous kyphoplasty versus conservative treatment of acute and subacute osteoporotic vertebral compression fractures: a randomized controlled study. Chin J Orthop Trauma. 2011; 13: 719–724.
  37. 37. Berenson J, Pflugmacher R, Jarzem P, Zonder J, Schechtman K, Tillman JB, et al. Balloon kyphoplasty versus non-surgical fracture management for treatment of painful vertebral body compression fractures in patients with cancer: a multicentre, randomised controlled trial. Lancet Oncol. 2011; 12: 225–235. pmid:21333599
  38. 38. Farrokhi MR, Alibai E, Maghami Z. Randomized controlled trial of percutaneous vertebroplasty versus optimal medical management for the relief of pain and disability in acute osteoporotic vertebral compression fractures. J Neurosurg Spine. 2011; 14: 561–569. pmid:21375382
  39. 39. Blasco J, Martinez-Ferrer A, Macho J, San Roman L, Pomés J, Carrasco J, et al. Effect of vertebroplasty on pain relief, quality of life, and the incidence of new vertebral fractures: a 12-month randomised follow-up, controlled trial. J Bone Miner Res. 2012; 27: 1159–1166. pmid:22513649
  40. 40. Munk PL, Liu DM, Murphy KP, Baerlocher MO. Effectiveness of vertebroplasty: a recent controversy. Can Assoc Radiol J. 2009; 60: 170–171. pmid:19782885
  41. 41. Aebi M. Vertebroplasty:about sense and nonsense of uncontrolled “controlled randomized prospective trials”. Eur Spine J. 2009; 18: 1247–1248. pmid:19756780
  42. 42. Kallmes D, Buchbinder R, Jarvik J, Heagerty P, Comstock B, Turner J, et al. Response to "randomized vertebroplasty trials: bad news or sham news?". Am J Neuroradiol. 2009; 30: 1808–1809. pmid:19815617
  43. 43. Klotzbuecher CM, Ross PD, Landsman PB, Abbott TA, Berger M. Patients with prior fractures have an increased risk of future fractures: a summary of the literature and statistical synthesis. J Bone Miner Res. 2000; 15: 721–739. pmid:10780864
  44. 44. Staples MP, Kallmes DF, Comstock BA, Jarvik JG, Osborne RH, Heagerty PJ, et al. Effectiveness of vertebroplasty using individual patient data from two randomised placebo controlled trials: meta-analysis. BMJ. 2011; 343: d3952. pmid:21750078
  45. 45. Schulz KF, Altman DG, Moher D. CONSORT 2010 statement: updated guidelines for reporting parallel group randomised trials. BMC medicine. 2010; 8: 18. pmid:20334633