Skip to main content

Efficacy of various core decompression techniques versus non-operative treatment for osteonecrosis of the femoral head: a systemic review and network meta-analysis of randomized controlled trials

Abstract

Background

Various Joint-preserving therapy (JPT) methods have been performed and tried in recent decades, but their results and efficacy were inconsistent and controversial. The purpose of this study is to evaluate its effectiveness and whether there are statistical differences in treatment between different interventions based on published RCT studies.

Methods

Following the PRISMA-NMA checklist, Medline, EMBASE, Web of Science, and Cochrane Library databases were searched and collected related RCT studies. The sources were searched from inception up to October 30, 2020. The primary outcomes including the rate of radiographic progression and conversion to THA and the secondary outcome -Harris Hip Scores (HHS) were extracted and compared in a Network meta-analysis.

Results

Seventeen RCT studies involving 784 patients (918 hips) with seven interventions including CD (core decompression), CD + BG (bone graft), CD + TI (tantalum rod implantation), CD + CT (Cell therapy), CD + BG + CT, VBG (vascularized bone graft), and nonsurgical or conservative treatment for ONFH were evaluated. In the radiographic progression results, CD + CT showed a relatively better result than CD, CD + BG and non-surgical treatment, the surface under the cumulative ranking curve (SUCRA) plot displayed that CD + CT (96.4%) was the best, followed by CD (64.1%).In conversion to THA results, there were no significant differences between the JPT methods and non-surgical treatment. In HHS, there was also no significant difference, other than CD + BG showed a statistical difference than non-surgical treatment only in terms of Cis, but the SUCRA was highest in non-surgical treatment (80.5%) followed by CD + CT (72.8%).

Conclusions

This Net-work meta-analysis demonstrated that there was no statistical difference in the outcome of radiographic progression and conversion to THA, also in HHS, other than CD + CT showed a relatively superior result in radiographic progression than nonsurgical treatment, namely, it’s maybe an effective method for delaying disease progression or reducing disease development based on current evidence.

Peer Review reports

Background

Osteonecrosis of the femoral head (ONFH) is a common but refractory disease in the orthopedics field. The initial manifestations are localized, partial necrosis, but with the development of advanced hip joint disease, it may progress to complete elimination of femoral head.

The annual incidence in the USA was estimated to be between approximately 10,000 and 20,000 cases [1]. and 0.01% in the German-speaking countries, with 5000 to 7000 persons affected [2]. If there is no timely and effective treatment in the early stage, 80% of cases will have femoral head collapse and end-stage degenerative joint disease within 2 years, and eventually need to total hip arthroplasty (THA) [3,4,5]. The THA method has good function improvement and pain relief [6,7,8], but its application in young patients faces some problems. For example, the prosthetic replacements rarely last for a lifetime and bring a huge financial burden increasing the overall cost of managing this condition due to the requirement for revision THA [9, 10] between ages of 30–50 years considered to be the most susceptible [5, 11, 12]. The principles for considering ONFH treatment include the termination of pathologic progression and the restoring of weight-bearing capacity, many different joint-preserving therapy (JPT) methods have been performed in recent decades-years. Based on published data in the USA by Sodhi, N [13], although there was an increasing rate of THA for ONFH (75 to 88%) [14] during 1992 to 2008, decreased during 2009 to 2015 and found that the rate of joint-preserving procedures showed a trend of relative growth, especially in patients aged <50 years.

Until now, various joint-preserving therapies (JPT) have been further explored with promising results, including core decompression (CD), Extracorporeal shockwave therapy,

vascularized and non-vascularized bone graft, CD combined with bone mesenchymal stem cells (BMSC) or other bone marrow cells and applications of biomaterials like tantalum implantation et al. before the femoral head collapse. Each has its advantages, core decompression can decrease intraosseous pressure, alleviate bone marrow edema and improve blood supply for the femoral head [15,16,17], mesenchymal stem cells (MSCs) can release exosomes that contain cytokines promoting osteogenesis, chondrogenesis, and angiogenesis [18, 19]. Bone graft allows for subchondral bone remodeling and healing [20, 21] even tantalum rod implantation has become a good choice of mechanical substitute because of its superior strength, fatigue properties, biocompatibility [22]. And vascularized bone graft (VBG) provides structural support, but also restores vascular supply to enhance lesion healing [23,24,25]. Despite this, the results of treatment effect have been reported inconsistently from published studies and there was a lack of consensus as to which methods were more effective or superior.

Given the continuing uncertainties, this study, therefore, was designed as a systemic review and network meta-analysis to assess the effectiveness between various joint-preserving procedures and non-surgical conservative treatment for ONFH using an updated systematic review and meta-analysis including all relevant RCTs published to date to provide the selection and application of clinical treatment.

Methods

Protocol and registration

This systemic review and Network Meta-analysis (NMA) were conducted following the Preferred Reporting Items for Systemic Reviews and Meta-analyses for Network Meta-analysis (PRISMA-NMA) reporting guideline [26]. The protocol has been registered in PROSPERO with the registration No: CRD42020214489.

Search strategy

Ovid Medline, EMBASE, Web of Science, and Cochrane Library databases were searched to collect all published evidence from inception up to and including Oct 30, 2020. Search terms included extensive controlled vocabulary in various combinations, supplemented with keywords including ‘Femur Head’, ‘Joints’, ‘Osteonecrosis’, ‘Necrosis’, ‘Orthopedic Procedures’. The search strategy used in Medline via OVID is presented in Appendix 1. Besides, the reference reports of previous systematic reviews, meta-analyses, and randomized controlled trials (RCTs) were manually reviewed.

Eligibility criteria

Only RCTs were included. The PICO information was as follows: patients(P): the patients who were diagnosed as ONFH and more than 18 years age; intervention(I): various joint-preserving procedures including non-vascular or vascular bone graft, tantalum implantation, cell-therapy (CT) including Mesenchymal stem cells, bone marrow aspirate concentrate, bone marrow mononuclear cells, et al. and non-surgical or physiotherapy treatment; Comparison(C): different types of treatment as a direct or indirect comparison; Outcome measures(O): the primary outcome were the rate of conversion to total hip replacement arthroplasty (THA); the rate of radiographic progressions to next stage; the secondary outcome was HHS (Harris Hip Score) to assess functional recovery; The study design (SD): RCT. The language was limited to English.

The exclusion criteria were as follows: (1) non-RCT, laboratory scientific or other non-relevant studies; (2) the study shared the same data set; (3) the study combined drug therapy effect with interventions or osteotomy. (4) the study focused on undesired outcomes or interventions. (5) literature report could not be extracted or converted into valid data.

Data extraction and outcome assessment

The following information was extracted independently: the first author; publication year; sample size; the number of hips; type of intervention; sex ratio; age; stage (ARCO or Ficat or Steinberg); risk factors and follow-up time. All treatments using cell extraction in ONFH treatment are classified as cell therapy (CT) owing to no uniform standard for cell extraction and classified vascular and avascular bone graft as VBG and BG according to whether vessels were used to supply blood. And non-surgical treatment includes a variety of physical and rehabilitation training such as physical shockwave therapy. The risk factors and clinical stages were also extracted and analyzed for statistical differences, because they maybe a potential interference factor and affect the results.

Clinical primary outcomes containing the number of conversions to THA and radiographic progression to the next stage. The secondary outcome of interest was the HHS (Harris Hip Score) to assess clinic function (pain, joint activity, absence of deformity, and range of motion). The maximum score is 100 and higher indicates a better treatment result. Because the postoperative follow-up time was different, all the data results were based on the last follow-up reported outcomes of each study.

Risk of Bias assessment

The Cochrane Collaboration’s risk of bias tool [27] was used to assess bias according to Review Manager (version 5.3). The disagreements were resolved by the third reviewer and the methodology for each study was graded as ‘high’, ‘low’, or ‘unclear’ reflecting the risk of bias.

Statistical analysis

A multiple treatment comparison NMA was performed under a frequentist framework using a random-effects model. The network and mvmeta packages in Stata statistical software version 14.0 MP (State Corp) [28, 29] were used to analyze the data. The network plots were used to summarized geometry of the evidence network indicate the type of various interventions, the number of patients, and the amount of pair-wise comparison. The consistency of the network was checked with local and global inconsistency tests. Each closed loop in the network was assessed to confirm local inconsistency between direct and indirect effect estimates and only triangular (formed by three treatments all compared with one another) loops were considered.

The summary of mean differences and 95% confidence intervals (Cis) together with their predictive intervals (PrIs) were presented between comparisons. PrIs provide an interval within which the estimate of a future study is expected to be.

The surface under the cumulative ranking curve (SUCRA) is a relative ranking measure that accounts both for the location and the variance of all relative treatment effects [30]. A lower SUCRA value was regarded as a better result for the primary outcome and a higher SUCRA value was regarded as a better result for the secondary outcome. A comparison-adjusted funnel plot was used to assess the presence of small-study effects [31].

Results

Baseline characteristics of included studies

A PRISMA diagram summarizes the literature search results and study selection for this systemic review and NMA is shown in Fig. 1. Of the 7896 citations identified through our literature search (1702 after duplicates were removed), 6162 were deemed ineligible after the title and abstract screening, leaving 32 to articles search for full-text review. In total, 17 RCTs [15, 17, 32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47] involving 784 patients (918 hips) met the inclusion criteria and were accepted. Including non-surgical treatment, Core decompression (CD), CD + bone graft (BG), CD + TI (tantalum rod implantation), CD + Cell therapy (CT), CD + BG + CT and vascularized bone graft (VBG). The basic characteristics of the included studies are summarized in Table 1.

Table 1 Basic characteristics of the included studies

Risk of bias of included researches

The risk of bias of the included studies in this NMA was generally unclear or high. Overall, studies fulfilled the criteria for a judgment of a high risk of bias. Details about the risk of bias assessment were graphically summarized in Fig. 2. The study was deemed high risk.

Results of meta-analysis

Figure 3 A and B showed the network plot of the risk factors induced to ONFH and the proportion of stage 3 in each intervention, respectively. And the results showed that there was no significant statistical difference between each intervention in Figure 4.

Radiographic progression

Figure 3.C depicted the network plot of the various JPT methods comparing the rate of radiographic progression results. Seven interventions (CD, CD + BG, CD + TI, CD + CT, CD + BG + CT,VBG, and non-surgical treatment) were compared in 15 studies [15, 17, 32,33,34,35,36, 38, 39, 41,42,43,44, 46, 47] and pooled results. CD and CD + CT were compared directly more than the other treatment. CD and CD + CT was the most frequent comparator in our studies. Three comparisons (CD + BG vs CD + BG + CT, CD + BG vs VBG and CD vs CD + CT) were conducted using direct evidence alone. Five comparisons were performed using mixed evidence (both direct and indirect evidence) and 13 comparisons using indirect evidence alone.

Fig. 1
figure 1

PRISMA flow diagram details the process of relevant clinical study selection

Fig. 2
figure 2

Details about the risk of bias assessment

Fig. 3
figure 3

Network plot of the direct comparisons of the outcomes for all included studies. The width of the lines is proportional to the number of trials comparing every pair of treatments, and the size of every node is proportional to the number of randomized participants (sample size). A) risk factor of ONFH, B) stage 3 C) radiographic progression D) conversion to THA, E) HHS, F) the inconsistency plots of the direct and indirect comparisons, in radiographic progression

Fig. 4
figure 4

Confidence intervals and predictive intervals of the estimates of outcomes of risk factor of ONFH and stage 3. The black part corresponds to the 95% confidence interval and the red part to the 95% predictive interval. A) Steroid. B) Alcohol. C) Idiopathic. D) ONFH stage 3

Fig. 5
figure 5

Confidence intervals and predictive intervals of the estimates of outcomes. The black part corresponds to the 95% confidence interval and the red part to the 95% predictive interval. A) the rate of radiographic progression. B) the rate of conversion to THA. C) HHS

Fig. 6
figure 6

the Cumulative ranking curve of the outcomes of each JPT method. A) the rate of radiographic progression. B) the rate of conversion to THA. C) HHS

Fig. 7
figure 7

Comparison-adjusted funnel plots. A) the rate of radiographic progression. B) the rate of conversion to THA. C) HHS. 1: Non-surgical treatment. 2: Core decompression (CD). 3: CD + BG. 4: CD + TI. 5: CD + CT. 6: CD + BG + CT. 7: VBG

There were two closed loops and no significance in the local inconsistency between the direct and indirect point estimates (Fig. 3F), and no network inconsistency [χ2 (2) = 1.87, p = 0.392]. CD + CT showed a statistical difference and relatively superior result than non-surgical treatment, CD, and CD + BG, which were significant only in 95% Cis but not in 95% PrIs (Fig. 5A) which means that any future RCT could change the significance of the efficacy of these comparisons.

The cumulative ranking plot was drawn, and the SUCRA probabilities were calculated (Fig. 6A). According to the SUCRA value, CD + CT (96.4%) showed the relatively best result, followed by CD (64.1%), CD + BG + CT (59.2%), VBG (48.5%), CD + TI (43.3%), non-surgical treatment (24.3%) and CD + BG (14.3%). The comparison-adjusted funnel plots showed that the funnel plots were symmetrical around the zero lines, which suggested a less likely publication bias (Fig. 7A).

Conversion to THA

Figure 3D displayed the network graph of the seven interventions (CD, CD + BG, CD + TI, CD + CT, CD + BG + CT,VBG, and non-surgical treatment) that compared in 15 studies [15, 17, 32, 33, 35,36,37,38,39, 42,43,44,45,46,47] in terms of conversion to THA. CD and CD + CT were more studies when compared directly than the other JPT methods. Four comparisons (CD vs CT, CD + BG vs CD + TI, CD + BG vs CD + BG + CT, and CD + BG vs VBG) were conducted using direct evidence alone. Two comparisons were using mixed evidence and 15 comparisons using indirect evidence alone.

There was no available loop formed by the study arms, and loop-specific tests were not performed. No significant differences among the JPT methods in terms of both CIs and PrIs were found, other than CD + CT showed a lower rate than CD + BG only in terms of the Cis (Fig. 5B).

The SUCRA plots (Fig. 6B) showed that the rate of conversion to THA was lowest in CD + CT (90.4%), followed by CD (69.1%), CD + BG + CT (58%), VBG (47.6%), non-surgical (46.2%), CD + BG (24%), and CD + TI (14.8%). The comparison-adjusted funnel plots suggested a less likely publication bias (Fig. 7B).

Harris hip scores

The network plot comparing the HHS was depicted in Fig. 3E. Six JPT methods (CD, CD + BG, CD + TI, CD + BG + CT, VBG and non-surgical treatment) were compared in 7 studies [17, 32, 36,37,38, 41, 46]. Five comparisons were conducted using mixed evidence and 10 comparisons using the indirect evidence alone. There was no available loop formed by the study arms.

There was no significant difference among these methods in CIs and PrIs other than CD + BG showed a higher score than non-surgical treatment only in terms of Cis (Fig. 5C). The SUCRA plot displayed that the HHS (Fig. 6C) was the highest in non-surgical treatment (80.5%), CD + CT (72.8%), CD + TI (54.0%), CD (48.7%), VBG (34.8%) and CD + BG (9.2%). Publication bias was less likely in the comparison-adjusted funnel plot (Fig. 7C).

Discussion

. In recent years, many studies [15, 17, 32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47] have been made and various JPT methods have been carried out, but it remains challenges and controversies about efficacy. In our NMA, there was no statistical difference in radiographic progression and conversion to THA, also in HHS between JPT methods and non-surgical treatment, other than CD + CT showed a relatively superior result in radiographic progression.

Based on reported data in USA, THA was still the most commonly performed procedure for AVN and the annual percentage of patients managed using a THA accounted for 89.5% between 2009 and 2015, reported by Sodhi [13]. However, the success of non-replacement procedures is also critical to the patients’ quality of life and the impact on the healthcare system.

Simple core decompression (CD) has become the reference technique widely used in patients with early-stage ONFH Since popularized by Hungerford [48]. But the results of CD are always debated and controversial [11, 47, 49]. The efficacy of CD has been considered that it can decrease intraosseous pressure, alleviate bone marrow edema and improve blood supply for femoral head [15,16,17]. However, other studies [50,51,52] questioned and reported that, in fact, CD was not superior to non-surgical treatment, it cannot repair the femoral head which even lowers its biological strength and causes collapse. They found that when there is a subchondral fracture (47% in ARCO stage 3), compared with the pre-collapse stages (85% in ARCO stage 1 and 65% in ARCO stage 2), the success rate of core decompression is even worse [53, 54]. Koo KH at their RCT study also found that CD may be effective in symptomatic relief, but is of no greater value than conservative management in preventing collapse. Based on our NMA, there were no statistical differences in primary and secondary outcomes compared with other JPT methods and non-surgical treatment, although inferior to the CD + CT method in terms of radiographic progression.

Owing to CD’s unpredictable and different results especially in long-term results, and to improve the limitations, several other JPT methods have been proposed and improved in recent years and achieved some promising results on ONFH outcomes versus CD.

Cell therapy, especially stem cells, has been a research hotspot in recent years, and is used for tissue regeneration due to its ability to differentiate into multiple cell lineages [55]. It is generally believed that mesenchymal stem cells (MSCs) can release exosomes, which contain cytokines that promote bone formation, cartilage formation and angiogenesis, including bone morphogenetic protein 2, vascular endothelial growth factor and transforming growth factor β [18, 19]. Therefore, stem cell transplantation is expected to become a new method of ONFH combined with core decompression. The purpose of adding MSCs to the core decompression tunnel is to provide osteoprogenitor cells and vascular progenitor cells in the decompressed necrotic bone area to promote tissue regeneration and repair reported by Goodman et al. [56]. Since the CD + BMSCs for ONFH was proposed by Hernigou [57] et al. in 2006, many studies achieved their promising results. Gangji [44] et al. concluded that cell implantation delayed the progression of stage 1–2 osteonecrosis and decreased hip pain and joint symptoms more effectively than CD during sixty-month follow-up period. And at meta-analysis also found that it had better pain relief, clinical outcomes and provided a significant improvement in terms of survivorship over time compared with CD alone [58, 59].

However, there were also different results. Hauzer [35] at a double blind RCT comparing the CD with the CD + BMAC and found that implantation of it after CD did not produce any improvement of the evolution of ONFH in stage 3. Lim [60] et al. also assessed the clinical effects and radiological results according to a controlled trail and found that CD + CT method was ineffective in stage III–IV patients and there were no statistically significant differences between CD + CT and CD + BG in success rate or the clinical and radiographic results. In our NMA, we found that there was statistical difference and had relatively superior result than non-surgical treatment, CD, CD + BG and VBG in radiographic progression, but no in conversion to THA and HHS. Therefore, we think that it may be an effective method for delaying disease progression or reducing disease development based on current evidence especially in stage I and II.

Non-vascularized bone graft was also a choice for ONFH, Since Phemister [61] as one of first authors described the use of non-vascularized bone graft (NVBG) from tibia for ONFH. Multiple studies have shown that the success of this support following necrotic segment decompression to allow for subchondral bone remodeling and healing [20, 21]. Deqiang [38] et al. at RCT study reported that CD + BG can relieve hip pain, improve function with much lesser surgical trauma compared to VBG, so it is a better choice for ONFH. However, Wang C [46] reported that the shock-wave conservative treatment appeared to be more effective than CD + BG in early-stage ONFH, although the mechanism remains unknown. Based on our network results and rankings results, CD + BG had no obvious advantage in terms of primary and secondary outcomes and no statistically differences.

As a good choice of mechanical substitute, the technique of porous tantalum rod implantation (TI) was applied in medical science more than half a century [32], Because of its advantages of superior strength, fatigue properties, biocompatibility and initial stability for bones to those of natural osseous grafts, and they have low cytotoxicity and bacterial adhesion force [22]. Hua KC [62] at their meta-analysis showed that CD combined with TI showed satisfactory clinical results. However, some research argues that this method can only provide temporary structural support until new bone ingrowth in the necrotic lesion and the absence of new bone tissue growing into porous tantalum rod in necrotic lesions made this method less ideal [63, 64]. According to histopathologic search and analysis, the clinically failed implants found that among the 15 specimens, there were 14 cases of residual osteonecrosis, and all cases had subchondral fractures of the femoral head, among which 60% of the femoral head collapsed by Tanzer M [64]. Based on our study, CD + TI did not have significantly advantage as compared with other JPT methods in primary and secondary outcomes and no statistically difference.

VBG is also one of the popularized JPT methods for ONFH, some studies had showed that it was a better treatment option than CD combined with non-vascularized bone graft because not only provides structural support, but also restores vascular supply to enhance lesion healing [23,24,25]. However, high technical requirements and a relatively low success rate of surgery have to be considered. As reported, the failure rate of vascularized grafts ranging from 4 to 30% [65, 66] and most of them were found in chronic steroid users as reported in the literatures [67]. Meloni et al. [68] reported that vascularized fibular graft (VFG) failure appears to be related to the negative effect of creeping substitution and supports unbalanced bone resorption enhanced by corticosteroids. Although Ji Wang et al. [69] showed that VFG was superior effect on reducing treatment failure rates at their network meta-analysis, our results was not exactly consistent with them, the effect was not so superior compared other treatment. Although the risk factors for ONFH were not statistically different in each intervention, we found that chronic steroid-using is one of the main induce factor to ONFH and accounted for 25% (15/60) in the VBG group. This may be one of the main reasons for the difference. Reviewing the literature in our studies, VBG may be an effective treatment, but based on our results, considering various factors, VBG was not the best option treatment for ONFH especially in chronic steroid users.

There are several limitations in our NMA. First, this study did not make further analysis and summary according to the size and location of the necrotic lesion. Second, the adjuvant procedures and the follow-up time within each category were hard to be consistent. Third, the number of subjects was still limited and a larger scale RCT study will be necessary to confirm whether various joint-preserving procedures prevents the disease progression or are effective in ONFH. Fourth, the risk of bias of the included studies in this NMA was generally unclear or high, higher quality RCT research will be needed in the future.

Conclusion

This network meta-analysis assessed the various JPT methods containing the conservative non-surgical treatment in patients of ONFH. Although all available JPT methods have not been evaluated and further studies are needed, our NMA provides some important information about various methods of Joint-preserving treatment and references to select appropriate JPT methods in ONFH. The data suggest that there was no statistically difference in radiographic progression and conversion to THA, also in HHS between above JPT methods, other than CD + CT showed a relatively superior result in radiographic progression than nonsurgical treatment, namely, it’s an effective method for delaying disease progression or reducing disease development based on current evidence.

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Abbreviations

CD:

Core decompression

CD+BG:

CD+bone graft

CD+TI:

CD+tantalum rod implantation

CD+CT:

CD+Cell therapy

CD+BG+CT:

CD+bone graft+cell therapy

VBG:

Vascularized bone graft

ONFH:

Osteonecrosis of the femoral head

JPT:

Joint-preserving therapy

THA:

Total hip arthroplasty

HHS:

Harris Hip Score

References

  1. Moya Angeler J, Gianakos AL, Villa JC, Ni A, Lane JM. Current concepts on osteonecrosis of the femoral head. World J Orthop. 2015;6(8):590–601.

    Article  PubMed  PubMed Central  Google Scholar 

  2. Arbab D, König DP. Atraumatic femoral head necrosis in adults. Dtsch Arztebl Int. 2016;113(3):31–8.

    PubMed  PubMed Central  Google Scholar 

  3. Nam KW, Kim YL, Yoo JJ, Koo KH, Yoon KS, Kim HJ. Fate of untreated asymptomatic osteonecrosis of the femoral head. J Bone Joint Surg Am. 2008;90(3):477–84.

    Article  PubMed  Google Scholar 

  4. Min BW, Song KS, Cho CH, Lee SM, Lee KJ. Untreated asymptomatic hips in patients with osteonecrosis of the femoral head. Clin Orthop Relat Res. 2008;466(5):1087–92.

    Article  PubMed  PubMed Central  Google Scholar 

  5. Lavernia CJ, Sierra RJ, Grieco FR. Osteonecrosis of the femoral head. J Am Acad Orthop Surg. 1999;7(4):250–61.

    Article  CAS  PubMed  Google Scholar 

  6. Johannson HR, Zywiel MG, Marker DR, Jones LC, McGrath MS, Mont MA. Osteonecrosis is not a predictor of poor outcomes in primary total hip arthroplasty: a systematic literature review. Int Orthop. 2011;35(4):465–73.

    Article  PubMed  Google Scholar 

  7. Seyler TM, Cui Q, Mihalko WM, Mont MA, Saleh KJ. Advances in hip arthroplasty in the treatment of osteonecrosis. Instr Course Lect. 2007;56:221–33.

    PubMed  Google Scholar 

  8. Beaulé PE, Amstutz HC. Management of Ficat stage III and IV osteonecrosis of the hip. J Am Acad Orthop Surg. 2004;12(2):96–105.

    Article  PubMed  Google Scholar 

  9. Weber M, Renkawitz T, Voellner F, Craiovan B, Greimel F, Worlicek M, et al. Revision surgery in Total joint replacement is cost-intensive. Biomed Res Int. 2018;2018:8987104.

    Article  PubMed  PubMed Central  Google Scholar 

  10. Collins KD, Chen KK, Ziegler JD, Schwarzkopf R, Bosco JA, Iorio R. Revision Total hip Arthroplasty-reducing hospital cost through fixed implant pricing. J Arthroplast. 2017;32(9s):S141–s143.

    Article  Google Scholar 

  11. Zalavras CG, Lieberman JR. Osteonecrosis of the femoral head: evaluation and treatment. J Am Acad Orthop Surg. 2014;22(7):455–64.

    Article  PubMed  Google Scholar 

  12. Mont MA, Rajadhyaksha AD, Hungerford DS. Outcomes of limited femoral resurfacing arthroplasty compared with total hip arthroplasty for osteonecrosis of the femoral head. J Arthroplast. 2001;16(8 Suppl 1):134–9.

    Article  CAS  Google Scholar 

  13. Sodhi N, Acuna A, Etcheson J, Mohamed N, Davila I, Ehiorobo JO, Jones LC, Delanois RE, Mont MA: Management of osteonecrosis of the femoral head. Bone Joint J 2020, 102-b (7_Supple_B):122–128.

  14. Johnson AJ, Mont MA, Tsao AK, Jones LC. Treatment of femoral head osteonecrosis in the United States: 16-year analysis of the Nationwide inpatient sample. Clin Orthop Relat Res. 2014;472(2):617–23.

    Article  PubMed  Google Scholar 

  15. Stulberg BN, Davis AW, Bauer TW, Levine M, Easley K. Osteonecrosis of the femoral head. A prospective randomized treatment protocol. Clin Orthop Relat Res. 1991;268:140–51.

    Google Scholar 

  16. Kang P, Pei F, Shen B, Zhou Z, Yang J. Are the results of multiple drilling and alendronate for osteonecrosis of the femoral head better than those of multiple drilling? A pilot study. Joint Bone Spine. 2012;79(1):67–72.

    Article  PubMed  Google Scholar 

  17. Sen RK, Tripathy SK, Aggarwal S, Marwaha N, Sharma RR, Khandelwal N. Early results of core decompression and autologous bone marrow mononuclear cells instillation in femoral head osteonecrosis: a randomized control study. J Arthroplast. 2012;27(5):679–86.

    Article  Google Scholar 

  18. Fang S, Li Y, Chen P. Osteogenic effect of bone marrow mesenchymal stem cell-derived exosomes on steroid-induced osteonecrosis of the femoral head. Drug Des Devel Ther. 2019;13:45–55.

    Article  CAS  PubMed  Google Scholar 

  19. Larson E, Jones LC, Goodman SB, Koo KH, Cui Q. Early-stage osteonecrosis of the femoral head: where are we and where are we going in year 2018? Int Orthop. 2018;42(7):1723–8.

    Article  PubMed  Google Scholar 

  20. Pierce TP, Elmallah RK, Jauregui JJ, Poola S, Mont MA, Delanois RE. A current review of non-vascularized bone grafting in osteonecrosis of the femoral head. Curr Rev Musculoskelet Med. 2015;8(3):240–5.

    Article  PubMed  PubMed Central  Google Scholar 

  21. Pierce TP, Jauregui JJ, Elmallah RK, Lavernia CJ, Mont MA, Nace J. A current review of core decompression in the treatment of osteonecrosis of the femoral head. Curr Rev Musculoskelet Med. 2015;8(3):228–32.

    Article  PubMed  PubMed Central  Google Scholar 

  22. Zhang Y, Li L, Shi ZJ, Wang J, Li ZH. Porous tantalum rod implant is an effective and safe choice for early-stage femoral head necrosis: a meta-analysis of clinical trials. Eur J Orthop Surg Traumatol. 2013;23(2):211–7.

    Article  PubMed  Google Scholar 

  23. Eward WC, Rineer CA, Urbaniak JR, Richard MJ, Ruch DS. The vascularized fibular graft in precollapse osteonecrosis: is long-term hip preservation possible? Clin Orthop Relat Res. 2012;470(10):2819–26.

    Article  PubMed  PubMed Central  Google Scholar 

  24. Kim SY, Kim YG, Kim PT, Ihn JC, Cho BC, Koo KH. Vascularized compared with nonvascularized fibular grafts for large osteonecrotic lesions of the femoral head. J Bone Joint Surg Am. 2005;87(9):2012–8.

    Article  PubMed  Google Scholar 

  25. Korompilias AV, Beris AE, Lykissas MG, Kostas-Agnantis IP, Soucacos PN. Femoral head osteonecrosis: why choose free vascularized fibula grafting. Microsurgery. 2011;31(3):223–8.

    Article  PubMed  Google Scholar 

  26. Hutton B, Salanti G, Caldwell DM, Chaimani A, Schmid CH, Cameron C, et al. The PRISMA extension statement for reporting of systematic reviews incorporating network meta-analyses of health care interventions: checklist and explanations. Ann Intern Med. 2015;162(11):777–84.

    Article  Google Scholar 

  27. 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.

    Article  PubMed  PubMed Central  Google Scholar 

  28. Chaimani A, Higgins JP, Mavridis D, Spyridonos P, Salanti G. Graphical tools for network meta-analysis in STATA. PLoS One. 2013;8(10):e76654.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  29. IR W: Multivariate random-effects meta-regression: updates tomvmeta. Stata J 2011, 11:255–270.

  30. Salanti G, Ades AE, Ioannidis JP. Graphical methods and numerical summaries for presenting results from multiple-treatment meta-analysis: an overview and tutorial. J Clin Epidemiol. 2011;64(2):163–71.

    Article  PubMed  Google Scholar 

  31. Riley RD, Higgins JP, Deeks JJ. Interpretation of random effects meta-analyses. Bmj. 2011;342:d549.

    Article  PubMed  Google Scholar 

  32. Peng K, Wang Y, Zhu J, Li C, Wang Z. Repair of non-traumatic femoral head necrosis by marrow core decompression with bone grafting and porous tantalum rod implantation. Pakistan Journal of Medical Sciences. 2020;36(6):1392–6.

    Article  PubMed  PubMed Central  Google Scholar 

  33. Li M, Ma Y, Fu G, Zhang R, Li Q, Deng Z, Zheng M, Zheng Q: 10-year follow-up results of the prospective, double-blinded, randomized, controlled study on autologous bone marrow buffy coat grafting combined with core decompression in patients with avascular necrosis of the femoral head. Stem Cell Research and Therapy 2020, 11(1).

  34. Hu BJ, Gao DW, He YH. Efficacy of fibula fixation in the early treatment of osteonecrosis of the femoral head and its effects on local microcirculation, articular surface collapse, joint pain and function. Journal of Musculoskeletal Neuronal Interactions. 2018;18(1):55–61.

    PubMed  PubMed Central  Google Scholar 

  35. Hauzeur JP, De Maertelaer V, Baudoux E, Malaise M, Beguin Y, Gangji V. Inefficacy of autologous bone marrow concentrate in stage three osteonecrosis: a randomized controlled double-blind trial. Int Orthop. 2018;42(7):1429–35.

    Article  PubMed  Google Scholar 

  36. Cao L, Guo C, Chen J, Chen Z, Yan Z. Free vascularized fibular grafting improves vascularity compared with Core decompression in femoral head osteonecrosis: a randomized clinical trial. Clin Orthop Relat Res. 2017;475(9):2230–40.

    Article  PubMed  PubMed Central  Google Scholar 

  37. Pepke W, Kasten P, Beckmann NA, Janicki P, Egermann M. Core decompression and autologous bone marrow concentrate for treatment of femoral head osteonecrosis: a randomized prospective study. Orthop Rev. 2016;8(1):5–9.

    Article  Google Scholar 

  38. Deqiang Li ML. Peilai Liu: Core decompression or quadratus femoris muscle pedicle bone grafting for nontraumatic osteonecrosis of the femoral head: a randomized control study. Indian J Orthop. 2016;50:629–35.

    Article  PubMed  PubMed Central  Google Scholar 

  39. Tabatabaee RM, Saberi S, Parvizi J, Mortazavi SM, Farzan M. Combining concentrated autologous bone marrow stem cells injection with Core decompression improves outcome for patients with early-stage osteonecrosis of the femoral head: a comparative study. J Arthroplast. 2015;30(9 Suppl):11–5.

    Article  Google Scholar 

  40. Qiang Mao WW, Xu T. Combination treatment of biomechanical support and targeted intra-arterial infusion of peripheral blood stem cells mobilized by granulocyte-colony stimulating factor for the osteonecrosis of the femoral head: a randomized controlled clinical trial. J Bone Miner Res. 2015;30:647–56.

    Article  PubMed  Google Scholar 

  41. Miao HYD, Liang W, Yao Y. Effect of osteonecrosis intervention rod versus Core decompression using multiple small Drill holes on early stages of necrosis of the femoral head: a prospective study on a series of 60 patients with a minimum 1-year-follow-up. Open Orthop J. 2015;9:179–84.

    Article  PubMed  PubMed Central  Google Scholar 

  42. Ma Y, Wang T, Liao J, Gu H, Lin X, Jiang Q, et al. Efficacy of autologous bone marrow buffy coat grafting combined with core decompression in patients with avascular necrosis of femoral head: a prospective, double-blinded, randomized, controlled study. Stem Cell Res Ther. 2014;5(5):115.

    Article  PubMed  PubMed Central  Google Scholar 

  43. Zhao D, Cui D, Wang B, Tian F, Guo L, Yang L, et al. Treatment of early stage osteonecrosis of the femoral head with autologous implantation of bone marrow-derived and cultured mesenchymal stem cells. Bone. 2012;50(1):325–30.

    Article  PubMed  Google Scholar 

  44. Gangji V, De Maertelaer V, Hauzeur JP. Autologous bone marrow cell implantation in the treatment of non-traumatic osteonecrosis of the femoral head: five year follow-up of a prospective controlled study. Bone. 2011;49(5):1005–9.

    Article  PubMed  Google Scholar 

  45. Neumayr LD, Aguilar C, Earles AN, Jergesen HE, Haberkern CM, Kammen BF, et al. Physical therapy alone compared with core decompression and physical therapy for femoral head osteonecrosis in sickle cell disease. Results of a multicenter study at a mean of three years after treatment. J Bone Joint Surg (Am Vol). 2006;88(12):2573–82.

    Article  Google Scholar 

  46. Wang CJ, Wang FS, Huang CC, Yang KD, Weng LH, Huang HY. Treatment for osteonecrosis of the femoral head: comparison of extracorporeal shock waves with core decompression and bone-grafting. J Bone Joint Surg Am. 2005;87(11):2380–7.

    PubMed  Google Scholar 

  47. Koo KHKR, Ko GH, Song HR, Jeong ST, Cho SH. Preventing collapse in early osteonecrosis of the femoral head. A randomised clinical trial of core decompression. J Bone Joint Surg Br. 1995;77:870–4.

    Article  CAS  PubMed  Google Scholar 

  48. Marker DR, Seyler TM, Ulrich SD, Srivastava S, Mont MA. Do modern techniques improve core decompression outcomes for hip osteonecrosis? Clin Orthop Relat Res. 2008;466(5):1093–103.

    Article  PubMed  PubMed Central  Google Scholar 

  49. McGrory BJ, York SC, Iorio R, Macaulay W, Pelker RR, Parsley BS, et al. Current practices of AAHKS members in the treatment of adult osteonecrosis of the femoral head. J Bone Joint Surg Am. 2007;89(6):1194–204.

    Article  PubMed  Google Scholar 

  50. Hong YC, Zhong HM, Lin T, Shi JB. Comparison of core decompression and conservative treatment for avascular necrosis of femoral head at early stage: a meta-analysis. Int J Clin Exp Med. 2015;8(4):5207–16.

    PubMed  PubMed Central  Google Scholar 

  51. Li X, Xu X, Wu W. Comparison of bone marrow mesenchymal stem cells and core decompression in treatment of osteonecrosis of the femoral head: a meta-analysis. Int J Clin Exp Pathol. 2014;7(8):5024–30.

    PubMed  PubMed Central  Google Scholar 

  52. Castro FP Jr, Barrack RL. Core decompression and conservative treatment for avascular necrosis of the femoral head: a meta-analysis. Am J Orthop (Belle Mead NJ). 2000;29(3):187–94.

    Google Scholar 

  53. Mont MA, Carbone JJ, Fairbank AC. Core decompression versus nonoperative management for osteonecrosis of the hip. Clin Orthop Relat Res. 1996;324:169–78.

    Article  Google Scholar 

  54. Mont MA, Cherian JJ, Sierra RJ, Jones LC, Lieberman JR. Nontraumatic osteonecrosis of the femoral head: where do we stand today? A ten-year update. J Bone Joint Surg Am. 2015;97(19):1604–27.

    Article  PubMed  Google Scholar 

  55. Oryan A, Kamali A, Moshiri A, Baghaban Eslaminejad M. Role of Mesenchymal stem cells in bone regenerative medicine: what is the evidence? Cells Tissues Organs. 2017;204(2):59–83.

    Article  CAS  PubMed  Google Scholar 

  56. Goodman SB. The biological basis for concentrated iliac crest aspirate to enhance core decompression in the treatment of osteonecrosis. Int Orthop. 2018;42(7):1705–9.

    Article  PubMed  Google Scholar 

  57. Hernigou P, Habibi A, Bachir D, Galacteros F. The natural history of asymptomatic osteonecrosis of the femoral head in adults with sickle cell disease. J Bone Joint Surg Am. 2006;88(12):2565–72.

    Article  PubMed  Google Scholar 

  58. Wang Z, Sun QM, Zhang FQ, Zhang QL, Wang LG, Wang WJ. Core decompression combined with autologous bone marrow stem cells versus core decompression alone for patients with osteonecrosis of the femoral head: a meta-analysis. Int J Surg. 2019;69:23–31.

    Article  PubMed  Google Scholar 

  59. Andriolo L, Merli G, Tobar C, Altamura SA, Kon E, Filardo G. Regenerative therapies increase survivorship of avascular necrosis of the femoral head: a systematic review and meta-analysis. Int Orthop. 2018;42(7):1689–704.

    Article  PubMed  Google Scholar 

  60. Lim YW, Kim YS, Lee JW, Kwon SY. Stem cell implantation for osteonecrosis of the femoral head. Exp Mol Med. 2013;45(11):e61.

    Article  PubMed  PubMed Central  Google Scholar 

  61. Phemister DB. Treatment of the necrotic head of the femur in adults. J Bone Joint Surg Am. 1949;31a(1):55–66.

    Article  CAS  PubMed  Google Scholar 

  62. Hua KC, Yang XG, Feng JT, Wang F, Yang L, Zhang H, et al. The efficacy and safety of core decompression for the treatment of femoral head necrosis: a systematic review and meta-analysis. J Orthop Surg Res. 2019;14(1):306.

    Article  PubMed  PubMed Central  Google Scholar 

  63. Liu B, Sun W, Yue D, Li Z, Guo W. Combined tantalum implant with bone grafting for the treatment of osteonecrosis of the femoral head. J Investig Surg. 2013;26(3):158–62.

    Article  Google Scholar 

  64. Tanzer M, Bobyn JD, Krygier JJ, Karabasz D. Histopathologic retrieval analysis of clinically failed porous tantalum osteonecrosis implants. J Bone Joint Surg Am. 2008;90(6):1282–9.

    Article  CAS  PubMed  Google Scholar 

  65. Urbaniak JR, Coogan PG, Gunneson EB, Nunley JA. Treatment of osteonecrosis of the femoral head with free vascularized fibular grafting. A long-term follow-up study of one hundred and three hips. J Bone Joint Surg Am. 1995;77(5):681–94.

    Article  CAS  PubMed  Google Scholar 

  66. Zhang C, Zeng B, Xu Z, Sui S, Song W, Jin D, et al. Wang K: [treatment of osteonecrosis of femoral head with free vascularized fibula grafting]. Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2004;18(5):367–9.

    PubMed  Google Scholar 

  67. Yoo MC, Chung DW, Hahn CS. Free vascularized fibula grafting for the treatment of osteonecrosis of the femoral head. Clin Orthop Relat Res. 1992;277:128–38.

    Article  Google Scholar 

  68. Meloni MC, Hoedemaeker WR, Fornasier V. Failed vascularized fibular graft in treatment of osteonecrosis of the femoral head. A histopathological analysis. Joints. 2016;4(1):24–30.

    Article  PubMed  PubMed Central  Google Scholar 

  69. Wang J, Wang J, Zhang K, Wang Y, Bao X. Bayesian network Meta-analysis of the effectiveness of various interventions for nontraumatic osteonecrosis of the femoral head. Biomed Res Int. 2018;2018:2790163.

    PubMed  PubMed Central  Google Scholar 

Download references

Acknowledgements

Not applicable

Funding

No external funding was received for the initiation or completion of this study.

Author information

Authors and Affiliations

Authors

Contributions

JHL conceived the design of the study. QZL and WLG collected the data and were involved in the design of the study. QZL and WLG contributed to data analysis and prepared the manuscript. JHL, RL and QZL edited the manuscript. All authors have given approval to the final version of the manuscript to be published.

Corresponding author

Correspondence to Jae Hyup Lee.

Ethics declarations

Ethics approval and consent to participate

Not applicable.

Consent for publication

Not applicable.

Competing interests

All authors declare that they have no conflict of interest.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Additional file 1.

Appendix 1. Medline via OVID search strategy

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Liu, Q., Guo, W., Li, R. et al. Efficacy of various core decompression techniques versus non-operative treatment for osteonecrosis of the femoral head: a systemic review and network meta-analysis of randomized controlled trials. BMC Musculoskelet Disord 22, 948 (2021). https://doi.org/10.1186/s12891-021-04808-2

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12891-021-04808-2

Keywords