Abstract
Purpose
Fascia iliaca compartment block (FICB) provides an analgesic option for total hip arthroplasty (THA) patients. The evidence supporting FICB is still not well established. The purpose of this meta-analysis was to assess FICB for pain control in THA patients.
Methods
PubMed, Embase, Cochrane Library, and Chinese Wanfang database were interrogated from their inceptions to December 15, 2018. We included randomized controlled studies reported as full text, those published as abstracts only, and unpublished data, if available. Data were independently extracted by two reviewers and synthesized using a random-effects model or fixed-effects model according to the heterogeneity.
Results
A total of eight RCTs were finally included for meta-analysis. Compared with placebo, FICB could significantly reduce VAS pain scores at 1–8 h (WMD = − 0.78, 95% CI [− 1.01, − 0.56], P = 0.000), 12 h (WMD = − 0.69, 95% CI [− 1.22, − 0.16], P = 0.011), and 24 h (WMD = − 0.46, 95% CI [− 0.89, − 0.02], P = 0.039). Compared with the control group, FICB could significantly decrease the occurrence of nausea and length of hospital stay (P < 0.05). There was no significant difference between the VAS pain score at 48 h and risk of fall between the FICB and the control groups (P > 0.05).
Conclusions
FICB could be used to effectively reduce pain intensity up to 24 h, total morphine consumption, and length of hospital stay in THA patients. Optimal strategies of FICB need to be studied in the future.
Similar content being viewed by others
Introduction
Total hip arthroplasty (THA) is a well-known popular surgical procedure for hip diseases, including end-stage hip osteoarthritis and femur neck fracture [1, 2]. THA is a well-known cause of severe postoperative pain. Non-steroidal antiinflammatory drugs (NSAIDs) and morphine were commonly used for pain control in THA patients [2]. These drugs were related to digestive tract side effects, and patients could not tolerate these complications [3, 4]. Thus, adequate pain control after THA is crucial for early ambulation and patient satisfaction.
Fascia iliaca compartment block (FICB) is an analgesic technique that involves injecting local anesthetic under the fascia of the iliacus muscle [5, 6]. FICB can be performed either guided by ultrasound or with a loss of resistance (LOR) technique. The evidence supporting FICB for pain control for THA patients is still not well established. Several RCTs have been published concerning FICB for THA patients. However, there was no consensus about the real efficacy of FICB in THA patients. Desmet et al. [7] revealed that longitudinal suprainguinal FICB reduces postoperative morphine requirements after anterior approach THA. Perry et al. [8] found that FICB has comparable pain control with psoas compartment block. The samples of published literature are limited, and the statistic power is limited. However, Aprato et al. [9] revealed that intra-articular hip injection provides better pre-operatory pain management in elder patients with intracapsular hip fractures compared to the FICB.
Therefore, we performed a meta-analysis of randomized controlled trials to compare the effect of FICB versus control on the pain intensity and morphine consumption in patients undergoing THA. We hypothesized that FICB compared with placebo is associated with decreased pain intensity in patients undergoing THA. Additionally, we assessed the efficacy and safety of FICB with respect to morphine consumption, risk of fall, and nausea.
Materials and methods
This meta-analysis was programed on the basis of the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement guidelines [10]. There was no registered protocol for this meta-analysis.
Search strategy
We performed a systematic electronic search in PubMed, Embase, the Cochrane library, and Chinese Wanfang database from inception through September 1, 2018. We conducted electronic searches using exploded Medical Subject Headings (MeSH) terms and corresponding key words. The search terms used in PubMed were listed in Additional file 1. No language restriction was applied. We also manually checked the bibliographies of previous reviews and included trials to identify other potentially eligible trials.
Inclusion criteria
Published RCTs meeting the following criteria were included: (1) population: adult patients and prepared for THA, (2) intervention: single administration FICB for pain control, (3) comparison: placebo or saline, and (4) ≥ 1 of the following outcomes: visual analog scale (VAS) at 6–8 h, 12 h, 24 h, and 48 h; total morphine consumption; occurrence of nausea; and occurrence of fall.
Study selection
After the duplicates were removed and the study selection process was completed, the titles and abstracts were scanned by two independent investigators. The relevant data were extracted by adopting a predetermined standardized procedure, which involved the first authors, year of publication, country, demographic characteristics of the participants, and the treatment regimen for each group. All data were verified for internal consistency, and controversies were settled by consensus or discussion with a third author. When inadequate information existed in the studies, contacting the first authors to obtain and clarify the relevant data were essential as specified by the standardized protocol.
Quality assessment
Cochrane collaboration’s tool for assessing the risk of bias was used to evaluate methodological quality of included trials. This tool focuses on the internal validity of the trial and assessment of risk of possible bias in different phases of trial conduct. The following items were assessed: random sequence generation, allocation concealment, blinding of participants, personnel and outcome assessment, incomplete outcome measures, selective outcome reporting, and other types of bias. Each item was qualified as low risk (L), unclear risk (U), or high risk (H). All assessments were conducted by two reviewers, independent of each other. Controversies were settled by consensus or discussion with a third author.
Data extraction
Two authors independently extracted the information from the original studies using a standardized data abstraction list, including study characteristics (such as author, publication year, country), patient characteristics (such as number of patients, mean age, gender, and female patients), intervention details for each treatment group (intervention type, dose, drugs and regimens), and outcome measures (VAS at 6–8 h, 12 h, 24 h, 48 h; total morphine consumption; occurrence of nausea; and occurrence of fall). Data were abstracted from the article text, tables, and graphs.
Data synthesis and statistical methods
In this meta-analysis, effect sizes for dichotomous outcomes were expressed as relative risk (RR) with 95% confidence interval (CI). Mean difference (MD) and 95% CI were calculated for continuous outcomes. The effect sizes were computed by a random-effects model [11]. I2 statistic was used to estimate the heterogeneity, with values greater than 50% considered as significant heterogeneity [12]. Furthermore, we applied sensitivity analyses to verify the robustness of the study results by using removing trials one by one. Egger linear regression test and funnel plots were implemented to test the publication bias when more than ten publications were included [13]. P values < 0.05 denoted statistically significant differences. Data analysis was conducted with Stata 12.0 (Stata Corp., College Station, TX, USA).
Results
Search results
The PRISMA statement flowchart shows the process of literature screening, study selection, and reasons for exclusion (Fig. 1). Our initial search yielded 556 potential studies. After removing duplicates by Endnote Software (Version X7, Thompson Reuters, CA, USA) and screening the titles and abstracts, eight RCTs were included in this meta-analysis [7, 14,15,16,17,18,19,20].
General characteristic
Characteristics and demographics of the included studies were presented in Table 1. These trials were published from 2009 to 2017. Population sizes ranged from 11 to 43, with a total of 372 patients (FICB = 186, control = 186). In the included studies, age ranged from 54 to 71.2 years. Protocol of FICB included ropivacaine and bupivacaine combined with or no epinephrine. Dose of infiltration drugs ranged from 30 to 50 ml. Only one study reported complication (hematoma) about FICB. Most of the included studies were performed with a relative short follow-up.
Risk of bias
Figures 2 and 3 describe the risk of bias summary and risk of bias graph, respectively. Overall, two trials were categorized as being at low risk of bias, four as being unclear, and two as being at high risk of bias.
Results of meta-analysis
VAS at 1–8 h, 12 h, 24 h, and 48 h
The VAS pain scores after treatment for 1–8 h weeks were reported in four trials. There was a little heterogeneity between the included studies (I2 = 9.3%, P = 0.356); fixed-effects model was adapted to analyze the results. The result revealed that that FICB was superior to control in terms of VAS pain scores after intervention for 1–8 h (WMD = − 0.78, 95% CI [− 1.01, − 0.56], P = 0.000, Fig. 4a). There was a large heterogeneity between the included studies for VAS pain scores after treatment for 12 h (I2 = 81.7%, P = 0.000, Fig. 4b), 24 h (I2 = 73.6%, P = 0.001, Fig. 4c), and 48 h (I2 = 92.8%, P = 0.000, Fig. 4d). Random-effects model was performed for VAS pain score at 12 h, 24 h, and 48 h. Results have shown that FICB has a beneficial role in reducing VAS pain scores at 12 h (WMD = − 0.69, 95% CI [− 1.22, − 0.16], P = 0.011, Fig. 4b) and 24 h (WMD = − 0.46, 95% CI [− 0.89, − 0.02], P = 0.039, Fig. 4c). Pooled data found that no statistically significant difference was observed between the FICB group and the control group in terms of the VAS scores after treatment for 72 h (WMD = − 0.52, 95% CI [− 1.31, 0.28], P = 0.203, Fig. 4d).
Total morphine consumption
A total of five studies reported total morphine consumption between the FICB group and the control group. We applied a random-effects model to analyze the results since there was a large heterogeneity between the included studies (I2 = 80.01%, P = 0.000). The result shows that the FICB could significantly reduce total morphine consumption than the control group (WMD = − 23.35, 95% CI [− 40.53, − 6.18], P = 0.008, Fig. 5).
Length of hospital stay
A total of five studies reported the length of hospital stay between the FICB group and the control group. We applied a fixed-effects model to analyze the results since there was no heterogeneity between the included studies (I2 = 0.0%, P = 0.796). The result shows that the FICB could significantly reduce the length of hospital stay than the control group (WMD = − 0.97, 95% CI [− 1.34, − 0.60], P = 0.000, Fig. 6).
The occurrence of nausea
Six studies involving 179 patients were available for analysis of the occurrence of nausea. The FICB led to significantly less occurrence of nausea than the control group (RR = 0.44, 95% CI [0.28 to 0.70], P = 0.000; I2 = 0.0%, P = 0.984, Fig. 7). Thus, we used a fixed-effects model to pool the relevant data.
The occurrence of fall
Six studies provided data on the occurrence of fall. FICB was not associated with an increase of the occurrence of fall (RR = 0.72, 95% CI [0.41 to 1.27], P = 0.260 Fig. 8). There was no heterogeneity between the included studies (I2 = 0.0%, P = 0.998); thus, we used a fixed-effects model to pool the occurrence of fall.
Publication bias, sensitivity analysis, and subgroup analysis
The funnel plot (Fig. 9) and Begg’s test (Fig. 10) showed no publication bias in the included studies.
Sensitivity analysis was performed by excluding one trail in turn and recalculating the pooled WMD for the remaining trials, which found that none of the studies affected the result (Fig. 11).
Discussion
Principal findings
The pooled results indicate that, according to available evidence, THA patient administration with FICB was associated with a reduction of pain intensity up to 24 h. What is more, FICB could significantly reduce total morphine consumption and the risk of nausea. However, there was no significant difference between the FICB and the control in the pain intensity at 48 h and risk of fall.
Relation to other systematic reviews
There were two meta-analyses comparing FICB and placebo that have been published [21, 22]. Zhang et al. [21] found that FICB has a beneficial role in controlling pain in total hip and knee arthroplasties. Limitation of this meta-analysis was obvious; THA and total knee arthroplasty were two different surgeries, and thus, pain intensity was different. Fei et al. [22] conducted a meta-analysis about FICB for pain control in lower limb surgery. Mixed different surgeries cause large clinical heterogeneity. In comparison, the current meta-analysis focused on THA only.
Implications for clinical practice
Our meta-analysis showed that the pain benefit existed in FICB compared with placebo. As we know, the femoral nerve and the lateral femoral cutaneous nerve innervate with the hip joint. FICB is injected through the iliac fascia cavity, which is constructed with the fascia as prezone and the iliopsoas as posterior. FICB could significantly block the femoral nerve, lateral femoral cutaneous nerve, and obturator nerve. Thus, FICB could decrease the pain intensity after THA. This beneficial effect was identified by previous trials. Besides, FICB is easy to administer, as it only requires ultrasound guidance. Steenberg et al. [23] performed a systematic review and revealed that FICB is an effective and relatively safe supplement in the preoperative pain management of hip fracture patients. The main outcome was consistent with our conclusion. Considering the results of the current meta-analysis and published studies, we suggest the administration FICB for pain control for THA patients.
Moreover, FICB could significantly decrease the morphine consumption and morphine-related complication (occurrence of nausea). McGraw-Tatum et al. [24] identified that FICB required less overall total opioids than the control group. And FICB is a relatively safe anesthesia technique as the needle point is away from the femoral nerve, femoral artery, and femoral vein [25].
Limitations
The present meta-analysis has some existing limitations that should be noted. First, only seven RCTs were included in this meta-analysis, and more high-quality studies are needed to confirm the above conclusions in the future. Second, patients were administered with different dose and regimes of FICB, which may lead to large heterogeneity. Third, the follow-up time in the included RCT was limited, and therefore, some adverse events may be underestimated. Fourth, a functional outcome is not performed due to the insufficiency of relevant data; future studies should observe the effects of FICB for hip function.
Conclusion
Our meta-analysis suggested that FICB but not placebo significantly reduced postoperative pain for THA patients. The use of FICB significantly reduced morphine consumption and the risk of nausea. FICB is recommended as an adjunct to multimodal anesthesia for THA patients. Future studies should explore optimal strategies (including drug and volume) of FICB.
Abbreviations
- CI:
-
Confidence intervals
- FICB:
-
Fascia iliaca compartment block
- NSAIDs:
-
Non-steroidal antiinflammatory drugs
- PRISMA:
-
Preferred Reporting Items for Systematic Reviews and Meta-Analyses
- RCTs:
-
Randomized controlled trials
- RR:
-
Risk ratio
- THA:
-
Total hip arthroplasty
- VAS:
-
Visual analog scale
- WMD:
-
Weighted mean difference
References
Sun L, Zhu X, Zou J, Li Y, Han W. Comparison of intravenous and oral acetaminophen for pain control after total knee and hip arthroplasty: a systematic review and meta-analysis. Medicine. 2018;97(6):e9751.
Liu G, Gong M, Wang Y, Xiang Z. Effect of methylprednisolone on pain management in total knee or hip arthroplasty: a systematic review and meta-analysis of randomized controlled trials. Clin J Pain. 2018;34(10):967–74.
Lindestrand AG, Christiansen ML, Jantzen C, van der Mark S, Andersen SE. Opioids in hip fracture patients: an analysis of mortality and post hospital opioid use. Injury. 2015;46(7):1341–5.
Aghayev E, Teuscher R, Neukamp M, Lee EJ, Melloh M, Eggli S, Roder C. The course of radiographic loosening, pain and functional outcome around the first revision of a total hip arthroplasty. BMC Musculoskelet Disord. 2013;14:167.
Guay J, Johnson RL, Kopp S. Nerve blocks or no nerve blocks for pain control after elective hip replacement (arthroplasty) surgery in adults. Cochrane Database Syst Rev. 2017;10:Cd011608.
Eyi YE, Arziman I, Kaldirim U, Tuncer SK. Fascia iliaca compartment block in the reduction of dislocation of total hip arthroplasty. Am J Emerg Med. 2014;32(9):1139.
Desmet M, Vermeylen K, Van Herreweghe I, Carlier L, Soetens F, Lambrecht S, Croes K, Pottel H, Van de Velde M. A longitudinal supra-inguinal fascia iliaca compartment block reduces morphine consumption after total hip arthroplasty. Reg Anesth Pain Med. 2017;42(3):327–33.
Perry CR Jr, Fahs AM, Kurdziel MD, Koueiter DM, Fayne RJ, Verner JJ. Intraoperative psoas compartment block vs preoperative fascia iliaca block for pain control after direct anterior total hip arthroplasty: a randomized controlled trial. J Arthroplast. 2018;33(6):1770–4.
Aprato A, Audisio A, Santoro A, Grosso E, Devivo S, Berardino M, Masse A. Fascia-iliaca compartment block vs intra-articular hip injection for preoperative pain management in intracapsular hip fractures: a blind, randomized, controlled trial. Injury. 2018;49(12):2203–8.
Knobloch K, Yoon U, Vogt PM. Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement and publication bias. J Craniomaxillofac Surg. 2011;39(2):91–2.
DerSimonian R, Laird N. Meta-analysis in clinical trials. Control Clin Trials. 1986;7(3):177–88.
Higgins JP, Thompson SG, Deeks JJ, Altman DG. Measuring inconsistency in meta-analyses. BMJ. 2003;327(7414):557–60.
Egger M, Davey Smith G, Schneider M, Minder C. Bias in meta-analysis detected by a simple, graphical test. BMJ. 1997;315(7109):629–34.
Badica IC, Pavelescu D, Badica L, Barbilian R, Grintescu I. The efficacy of fascia iliaca compartment block (FICB) for postoperative analgesia after hip arthroplasty (HA). Reg Anes Pain Med. 2010;35(5):E80.
Shariat AN, Hadzic A, Xu D, Shastri U, Kwofie K, Gandhi K, McCally CM, Gratenstein K, Vandepitte C, Gadsden J, et al. Fascia lliaca block for analgesia after hip arthroplasty: a randomized double-blind, placebo-controlled trial. Reg Anesth Pain Med. 2013;38(3):201–5.
Stevens M, Harrison G, McGrail M. A modified fascia iliaca compartment block has significant morphine-sparing effect after total hip arthroplasty. Anaesth Intensive Care. 2007;35(6):949–52.
Bang S, Chung J, Jeong J, Bak H, Kim D. Efficacy of ultrasound-guided fascia iliaca compartment block after hip hemiarthroplasty: a prospective, randomized trial. Medicine. 2016;95(39):e5018.
Goitia Arrola L, Telletxea S, Martinez Bourio R, Arizaga Maguregui A, Aguirre Larracoechea U. Fascia iliaca compartment block for analgesia following total hip replacement surgery. Rev Esp Anestesiol Reanim. 2009;56(6):343–8.
Deniz S, Atim A, Kurklu M, Cayci T, Kurt E. Comparison of the postoperative analgesic efficacy of an ultrasound-guided fascia iliaca compartment block versus 3 in 1 block in hip prosthesis surgery. Agri. 2014;26(4):151–7.
Lei G, Wu W, Li P, Zhang L, Wu G. The efficacy of ultrasound-guided continuous iliac fascia space block for postoperative analge-sia in elderly patients undergoing total hip replacement. Prac J Clin Med. 2016;13(2):114–7.
Zhang P, Li J, Song Y, Wang X. The efficiency and safety of fascia iliaca block for pain control after total joint arthroplasty: a meta-analysis. Medicine. 2017;96(15):e6592.
Fei D, Ma LP, Yuan HP, Zhao DX. Comparison of femoral nerve block and fascia iliaca block for pain management in total hip arthroplasty: a meta-analysis. Int J Surg. 2017;46:11–3.
Steenberg J, Moller AM. Systematic review of the effects of fascia iliaca compartment block on hip fracture patients before operation. Br J Anaesth. 2018;120(6):1368–80.
McGraw-Tatum MA, Groover MT, George NE, Urse JS, Heh V. A prospective, randomized trial comparing liposomal bupivacaine vs fascia iliaca compartment block for postoperative pain control in total hip arthroplasty. J Arthroplast. 2017;32(7):2181–5.
Mostafa SF, Eid GM, Elkalla RS. Patient-controlled fascia iliaca compartment block versus fentanyl patient-controlled intravenous analgesia in patients undergoing femur fracture surgery ☆. Egypt J Anal Chem. 2018;34(1):9–13.
Acknowledgements
We are grateful to all the patients and surgeons of the included studies.
Funding
None.
Availability of data and materials
As a meta-analysis, there are no patient data sets.
Author information
Authors and Affiliations
Contributions
XYZ and JBM conceived of the design of this meta-analysis. XYZ and JBM performed the literature retrieval and article writing. XYZ and JBM contributed to the data extraction, and JBM revised the manuscript. All authors read and approved the final manuscript.
Corresponding author
Ethics declarations
Ethics approval and consent to participate
Not applicable. This meta-analysis does not involve research on humans.
Consent for publication
Not applicable.
Competing interests
The authors declare that they have no competing interests.
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Additional file
Additional file 1:
Search strategies in PubMed (DOCX 14 kb)
Rights and permissions
Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.
About this article
Cite this article
Zhang, Xy., Ma, Jb. The efficacy of fascia iliaca compartment block for pain control after total hip arthroplasty: a meta-analysis. J Orthop Surg Res 14, 33 (2019). https://doi.org/10.1186/s13018-018-1053-1
Received:
Accepted:
Published:
DOI: https://doi.org/10.1186/s13018-018-1053-1