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Practice Rapid Recommendations

Low intensity pulsed ultrasound (LIPUS) for bone healing: a clinical practice guideline

BMJ 2017; 356 doi: https://doi.org/10.1136/bmj.j576 (Published 21 February 2017) Cite this as: BMJ 2017;356:j576

Population

Adults and children with a fracture or osteotomy

Choice of intervention

or LIPUS No ultrasound Standard care without ultrasound Low intensity pulsed ultrasound, used to stimulate bone growth (osteogenesis)

Recommendations

Population Favours LIPUS Favours no ultrasound

All Why? We recommend against the use of LIPUS Strong Benefits outweigh harms for almost everyone. All or nearly all informed patients would likely want this option. Strong Benefits outweigh harms for almost everyone. All or nearly all informed patients would likely want this option. Weak Benefits outweigh harms for the majority, but not for everyone. The majority of patients would likely want this option. Weak Benefits outweigh harms for the majority, but not for everyone. The majority of patients would likely want this option.

Comparison of benefits and harms Key practical issues Evidence quality Summary Favours LIPUS Favours no ultrasound See full details LIPUS No ultrasound 150 No important difference The panel unanimously agreed that all or nearly all informed patients would elect not to apply LIPUS. Preferences and values Resourcing Other considerations Days to radiographic healing Days to return to work Subsequent operations Device-related adverse effects LIPUS is a costly device which does not represent a wise use of health resources. Number of days (mean) 205 Events per 1000 people 160 0 0 147 200 No important difference 70 Pain score (0–100, lower better) Mean value 40 39 No important difference No important difference No important difference No important difference Days to full weight bearing 73 No important difference LIPUS may be burdensome to use. This is reflected in the TRUST trial, in which many patients reported limited compliance. Usually used for 15-20 minutes each day for 14 to 140 days No practical issues Device can be cumbersome to travel with Health insurance may not cover cost 128 LIPUS probably has little or no impact on time to radiographic healing Moderate Moderate quality evidence We are moderately confident in the evidence supporting the recommendation. Further research could have an important impact, which may change the estimates of effect. LIPUS probably has little or no impact on time to return to work Moderate Moderate quality evidence We are moderately confident in the evidence supporting the recommendation. Further research could have an important impact, which may change the estimates of effect. LIPUS has no impact on time to full weight bearing High High quality evidence We are very confident in the evidence supporting the recommendation. Further research is very unlikely to change the estimates of effect. LIPUS has no impact on pain reduction High High quality evidence We are very confident in the evidence supporting the recommendation. Further research is very unlikely to change the estimates of effect. LIPUS probably has little or no impact on subsequent operation Moderate Moderate quality evidence We are moderately confident in the evidence supporting the recommendation. Further research could have an important impact, which may change the estimates of effect. LIPUS has no impact on device-related adverse effects High High quality evidence We are very confident in the evidence supporting the recommendation. Further research is very unlikely to change the estimates of effect.

©BMJ Publishing Group Limited.

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Find recommendations, evidence summaries and consultation decision aids for use in your practice
  1. Rudolf W Poolman, chair, orthopaedic surgeon1,
  2. Thomas Agoritsas, assistant professor2 3,
  3. Reed A C Siemieniuk, methodologist2 4,
  4. Ian A Harris, professor of orthopaedic surgery5 6,
  5. Inger B Schipper, professor of trauma surgery7,
  6. Brent Mollon, orthopaedic surgeon8,
  7. Maureen Smith, patient representative9,
  8. Alexandra Albin, patient representative10,
  9. Sally Nador, patient representative11,
  10. Will Sasges, patient representative12,
  11. Stefan Schandelmaier, methodologist2 13,
  12. Lyubov Lytvyn, patient liaison expert14,
  13. Ton Kuijpers, methodologist15,
  14. Loes W A H van Beers, physiotherapist1 16,
  15. Michael H J Verhofstad, professor of trauma surgery17,
  16. Per Olav Vandvik, methods editor18 19
  1. 1Department of Orthopaedic Surgery, Joint Research, OLVG, 1090 HM Amsterdam, The Netherlands
  2. 2Department of Clinical Epidemiology and Biostatistics, McMaster University, Hamilton, Ontario, Canada L8S 4L8
  3. 3Division General Internal Medicine & Division of Clinical Epidemiology, University Hospitals of Geneva, CH-1211, Geneva, Switzerland
  4. 4Department of Medicine, University of Toronto, Toronto, Ontario, Canada M5G 2C4
  5. 5South Western Sydney Clinical School, UNSW Australia, Sydney NSW 2052, Australia
  6. 6Whitlam Orthopaedic Research Centre, Ingham Institute for Applied Medical Research, Liverpool, NSW 2170, Australia
  7. 7Department of Surgery, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands
  8. 8Orillia Soldiers’ Memorial Hospital, Orillia, Ontario, Canada L3V 5W6
  9. 9Ottawa, Ontario, Canada
  10. 10Society for Participatory Medicine Member, USA
  11. 11Kindred Northlake Hospital, Northlake, USA
  12. 12Calgary, Alberta, Canada
  13. 13Institute for Clinical Epidemiology and Biostatistics, University Hospital Basel, CH-4031 Basel, Switzerland
  14. 14Oslo University Hospital, Forskningsveien 2b, Blindern 0317 Oslo, Norway
  15. 15Dutch College of General Practitioners, 3502 GE Utrecht, The Netherlands
  16. 16Department of Physiotherapy, OLVG, 1090 HM Amsterdam, The Netherlands
  17. 17Trauma Research Unit Erasmus, Department of Surgery, Erasmus MC University Rotterdam, 3000 CA Rotterdam, The Netherlands
  18. 18Institute of Health and Society, Faculty of Medicine, University of Oslo, 0318 Oslo, Norway
  19. 19Department of Medicine, Innlandet Hospital Trust-division, Gjøvik, Norway
  1. Correspondence to: R W Poolman rwp{at}jointresearch.org

What you need to know

  • LIPUS is used for bone healing for people who have had fractures or osteotomy

  • LIPUS is costly to purchase

  • A new trial and linked systematic review provide moderate to high certainty evidence to support a strong recommendation against the use of LIPUS for bone healing

  • Further research is unlikely to alter the evidence

  • Healthcare administrators and funders may consider de-implementation of LIPUS as a performance indicator in quality improvement initiatives

Linked articles in this BMJ Rapid Recommendations cluster

  • Schandelmaier S, Kaushal A, Lytvyn L, et al. Low intensity pulsed ultrasound for bone healing: systematic review of randomized controlled trials. BMJ 2017;356:j656

    • Review of all available randomised trials that assessed LIPUS versus sham device or no device that informed the recommendation made by the panel

  • MAGICapp (www.magicapp.org)

    • Expanded version of the results with multilayered recommendations, evidence summaries, and decision aids for use on all devices

Does low intensity pulsed ultrasound (LIPUS) accelerate recovery in adults and children who have experienced bone fractures or osteotomy (cutting of a bone)? An expert panel rapidly produced these recommendations based on a linked systematic review triggered by a large multicentre randomised trial in adults with tibial fracture.

Fracture is common (see box 1). Bones can also be broken for medical reasons; osteotomy is a procedure whereby a bone is cut to shorten, lengthen, or to change its alignment. Following osteotomy, the bone has similar healing problems as traumatic fractures, and may require more extensive recovery.1

Box 1: Background information

Bone fracture
  • More than one in three people have a fracture at some point in their life

  • Each year around four per 100 people of all ages experience a fracture2

  • Some 5-10% of these experience delayed healing or non-union of the fracture3

LIPUS
  • Guidance

    • 1994 US Food and Drug Administration (FDA) approved LIPUS for fracture healing and, in 2000, for treatment of established non-unions4

    • 2010 UK National Institute for Health and Care Excellence (NICE) issued a statement supporting the use of LIPUS to reduce fracture healing time and to provide clinical benefit, particularly in circumstances of delayed healing and non-union5

  • Data on use

    • A Canadian survey of 450 trauma surgeons in 2008 found that nearly half of respondents were using bone stimulators to manage tibial fractures. Of those, about half used electromagnetic field therapy and the other half used LIPUS6

    • Global revenues for bone stimulators were about US$400m 2004.7 In 2007, sales from LIPUS were around $250m in the US8

    • We found no data to describe whether use has changed over time

Irrespective of age, location, and mechanism of the broken bone, whether it is managed with or without surgery, and whether it heals as expected or with delay, the idea of speeding or enhancing this healing to minimise symptoms and inconvenience for the patient is appealing. Bone stimulators such as LIPUS and electromagnetic field therapy might promote bone healing by stimulating bone growth (osteogenesis) in long or other bones.

Guidance from independent organisations on use of LIPUS for bone healing is scarce, but data suggest the device is commonly used in clinical practice (box 1). Prices vary across countries, each device costing between US$1300 and $5000 (based on US and UK).

The TRUST randomised controlled trial published in The BMJ on 25 October 2016 found that the addition of LIPUS to standard care in 501 adult patients undergoing surgery for fresh tibial fracture did not improve functional recovery or accelerate radiographic healing at one year follow up compared with a sham device.9 The BMJ Rapid Recommendations team believed that the TRUST trial, if considered in a new systematic review and meta-analysis, could change practice. Previous systematic reviews had concluded that potential benefits of LIPUS on bone healing were highly uncertain, with calls for trials with safeguards against bias and a focus on outcomes important to patients.10 11 The linked publications in this package (see “Linked articles” box) synthesise the latest evidence and translate it for clinical care.

How the recommendation was created

Our international guideline panel included orthopaedic and musculoskeletal trauma surgeons, physiotherapists, general internists, methodologists, and people with lived experience of bone fractures including one who used LIPUS (see appendix 1 on bmj.com for list of panel members). No person had financial conflicts of interest; intellectual and professional conflicts were minimised and managed according to BMJ Rapid Recommendations standards (see appendices 2 and 3 on bmj.com).

We followed the BMJ Rapid Recommendations procedures for creating a trustworthy recommendation.12 13 We discussed and agreed on the clinical outcomes of most importance to patients and clinicians a priori, and the systematic review authors focused their reporting on these. The outcomes chosen for LIPUS were:

  • Functional recovery (such as time to return to work and time to full weight bearing)

  • Pain

  • Subsequent operations

  • Complications.

The patient representatives judged radiographic healing as a less important outcome. It was included because many clinicians would consider radiographic healing to inform their management decisions. Some patients may feel reassured by observing radiographic healing, with increased confidence in resuming activities such as weight bearing and return to work.

Before seeing the evidence, we agreed on what would constitute an important benefit from using LIPUS for these outcomes, and how patient values and preferences might vary between persons. Guided by patients on our panel, we agreed that most people want at least a possibly important benefit in functional recovery time or pain to make the time and expense of using LIPUS worthwhile. Reduced adherence with the device in the TRUST trial suggests that LIPUS can be burdensome to patients.9

We applied the GRADE system to critically appraise the evidence and move from evidence to recommendations (appendix 3).14 We considered the balance of benefits, harms, and burdens of the procedure; the quality of evidence for each outcome; the typical and expected variation in patient values and preferences; resources; feasibility; and acceptability—details of our reasoning are summarised in the infographic and discussed further in the text.15 Recommendations can be strong or weak, for or against a course of action. We place a low value on speculative benefits of treatments. Thus, when available evidence suggests no benefit, or only very low quality evidence suggests benefit and moderate or high quality evidence shows appreciable adverse effects, burden, or cost, the panel would make a strong recommendation against an intervention.

The evidence

Evidence requested from the panel to inform recommendations:

  • A new rapid systematic review of the effects of LIPUS added to standard care for a variety of fractures and osteotomies16

  • A systematic literature search on patients’ values and preferences, which did not identify any relevant studies (see appendix 4 on bmj.com).

Systematic review of LIPUS for all fracture healing

The data from the TRUST trial9 were included in a linked systematic review of randomised trials of LIPUS compared with sham device or no device on patient-important outcomes in patients with a fracture or osteotomy. Fig 1 shows details about the trials and characteristics of included patients.16

Figure1

Fig 1 Characteristics of patients and trials included in systematic review of LIPUS

We judged that the systematic review provides evidence of moderate to high certainty that LIPUS has little or no impact on time to return to work, time to full weight bearing, pain, the number of subsequent operations, or time to radiographic healing (see infographic). We were confident that there was little risk of adverse events from the device, based on nine trials that reported this outcome.

For return to work, time to full weight bearing, and number of subsequent operations, our certainty in the evidence is moderate (rather than high) because of imprecise estimates of effect, where confidence intervals included potentially important benefit and harm (see forest plots (figs 2-7) in the linked systematic review).16 The observed heterogeneity in the effect sizes between trials for time to weight bearing, pain, and radiographic healing was explained by considering risk of bias: studies with serious methodological limitations due to lack of blinding (no use of sham device) suggested a benefit, whereas studies without such limitations did not (see subgroup analyses in the linked systematic review).16 For these outcomes, we therefore based our conclusions on the trials with low risk of bias. The estimates for typical (prognostic) outcomes for patients not treated with LIPUS were informed by the control arm of the TRUST trial, which enrolled patients with tibia fractures in the US and Canada and was at low risk of bias.

Understanding the recommendation

We unanimously agreed to issue a strong recommendation against LIPUS for patients with any bone fractures or osteotomy. We have moderate to high certainty of a lack of benefit for outcomes important to patients, and, combined with the high costs of treatment, LIPUS represents an inefficient use of limited healthcare resources.

A particular challenge for the panel was to determine to what extent the most trustworthy evidence—coming from trials of patients with fresh tibial and clavicle fractures managed operatively—could be applied to adults with different types of fracture or osteotomies. Trials including patients with stress fractures, non-union, and osteotomies were either at high risk of bias or did not contribute sufficient outcome data to the systematic review. After extensive deliberations, the panel found no compelling anatomical or physiological reasons why LIPUS would probably be beneficial in these other patient populations. For example, if LIPUS on fresh fractures does not decrease the incidence of non-unions, it is unlikely to exert a beneficial effect in the conversion of non-unions into healed bones. Furthermore, osteotomies have the same biological response as for traumatic fractures. An additional challenge faced by the panel was that no trials included children. Paediatric fractures typically heal faster and have lower rates of non-union; thus, any potential benefit of LIPUS for children is likely to be even smaller than that for adults. The panel concluded that the evidence was applicable to all of these groups, and did not downgrade their certainty in the evidence.20

In response to peer review comments, the panel again considered the applicability to other fractures and populations, in particular non-union fractures. Reviewers pointed to differing healing methods in non-union, and the potential that smaller effect sizes could make a difference to patients. Non-union is the result of impaired bone health, as seen in smokers and diabetics,21 or due to mechanical reasons such as large bone defects. There was high quality evidence showing a lack of benefit in accelerating healing for fresh fractures, thus it is unlikely that LIPUS would improve outcomes in patients with non-union. Given the panel’s judgment of an implausible benefit of LIPUS for patients with non-union, the panel chose to make a strong recommendation against LIPUS also for these patients.

Practical considerations

Patients with fractures may experience pain and limited mobility, particularly in the first two to three months. Driving and physical activity are limited during the recovery period. Figure 2 outlines the key practical issues for those considering LIPUS as an adjunct therapy in the management of bone fractures.

Figure2

Fig 2 Practical issues about use of LIPUS

Costs and resources

LIPUS does not represent an efficient use of health resources for individuals or health funders, given its lack of benefit on outcomes important to patients and its purchasing costs. Healthcare organisations that currently pay for LIPUS may reasonably choose to stop reimbursements based on best current evidence and our strong recommendation against LIPUS.

Future research

It is unlikely that new trials will alter the evidence. Fracture research should focus on other interventions that have a greater probability to speed up healing, such as surgical application of adjuvant biomaterials or extracorporeal shock wave therapy.22 23 Further trials of treatments for non-union fractures would be better compared with operative stabilisation, with or without autologous bone grafts. Research should also address de-implementation strategies for the use of LIPUS for bone healing.24

How patients were involved in the creation of this article

Four people with lived experience of bone fractures, one of whom had used LIPUS, were full panel members, participated in the teleconferences and email discussions, and met all authorship criteria. These panel members identified important outcomes and led the discussions about values and preferences. Return to work or regular activities and pain were weighed as of higher importance for patients than radiographic healing. The panel identified key practical issues including concerns with cost and access to LIPUS, as well as the burden of therapy. In light of the lack of efficacy, one patient panel member remarked, and the others agreed, that discussing LIPUS would unnecessarily take valuable time from the patient-clinician encounter, which is often already too short.

Footnotes

  • Related to: Research doi: 10.1136/bmj.j656
  • This BMJ Rapid Recommendations article is one of a series that provides clinicians with trustworthy recommendations for potentially practice changing evidence. BMJ Rapid Recommendations represent a collaborative effort between the MAGIC group (www.magicproject.org) and The BMJ. A summary is offered here and the full version including decision aids is on the MAGICapp (www.magicapp.org), for all devices in multilayered formats. Those reading and using these recommendations should consider individual patient circumstances and their values and preferences and may want to use consultation decision aids in MAGICapp to facilitate shared decision making with patients. We encourage adaptation of recommendations to allow contextualisation of recommendations and to reduce duplication of work. Those considering use or adaptation of content may go to MAGICapp to link or extract its content or contact The BMJ for permission to reuse content in this article. Series adviser Rafael Perera-Salazar.

  • Competing interests: All authors have completed the BMJ Rapid Recommendations interests form. The BMJ Rapid Recommendations team judged that no panel member declared financial, professional, or academic interests that precluded authorship. The declared interests for each panel member are in appendix 2 on bmj.com. No panel members declared any financial conflicts of interest related to this clinical question, specifically no financial ties to the bone stimulators industry. B Mollon uses bone stimulators in practice. T Agoritsas, RAC Siemieniuk, B Mollon, S Schandelmaier, L Lytvyn, and PO Vandvik participated in writing the complementary systematic reviews that formed the evidence base for this guideline. B Mollon was a co-author on a systematic review on this topic published in The BMJ in 2009, for which R Poolman wrote the editorial. No other panel member has previously formally made statements regarding LIPUS. This article was edited by H MacDonald at The BMJ who had no relevant financial or intellectual interests.

  • Transparency: R Poolman affirms that the manuscript is an honest, accurate, and transparent account of the study being reported; that no important aspects of the study have been omitted; and that any discrepancies from the study as planned (and, if relevant, registered) have been explained.

This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ .

References

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