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February 2007 • Vol. 3, No. 1
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Advancing Orthotic and Prosthetic Care Through Knowledge
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Donald R. Cummings, CP
Replacing the function and appearance of the human foot has long been a goal of prosthetists, engineers, and others involved in the rehabilitation of amputees. Since the 1950s and the introduction of the SACH foot, numerous organizations and individuals have applied the sciences of materials, engineering, biomechanics, and human movement to design innovative prosthetic feet and ankles. Recently, new prosthetic feet designs and enhancements have been introduced at a near dizzying pace. Many features are offered such as energy storage and release, accommodation to all sorts of terrain, powered components, and enhanced appeal through natural appearance, color variations, and even adjustable heel height. Behind these developments are scientists, engineers, manufacturers, and entrepreneurs who often do their own testing or may put their products through rigorous standardized engineering tests of strength, function, and durability. Others, such as prosthetists, physicians, therapists, and biomechanists, have attempted to study, classify, or compare feet through gait labs, energy consumption tests, perceptive analysis questionnaires, or functional outcome measures.
The end users of these prosthetic foot and ankle mechanisms are amputees of all ages and backgrounds worldwide, who represent an extensive array of functional and cosmetic needs and goals. Many patients are now marketed to directly by
component manufacturers and distributors. As a result, patients may often have a specific foot in mind when they see their
prosthetist. But how do prosthetists and physicians know which feet to recommend to patients that will best meet patients’ needs and best impact their function? Are there resources, publications, comparisons, and outcome studies on which practitioners can rely? How are future developments to be guided in a world where technology is vast but funding sources for providing care to amputees seem to be shrinking?
In an effort to answer these and other related questions, the Academy has embarked on a bold new venture to investigate the state of scientific literature that details the development, evaluation, and future of prosthetic foot/ankle mechanisms and multiple other topics related to the provision of prosthetic and orthotic services. The State-of-the-Science Conference (SSC) on Prosthetic Foot/Ankle Mechanisms was held in April 2005 at Texas Scottish Rite Hospital for Children in Dallas.
An SSC is designed first to provide a systematic review of literature and ranking of evidence on a conference topic. A
panel of experts is asked to evaluate this literature and develop statements that advance understanding in a way that will be
helpful to health professionals and the public. The conference may also serve to document clinical belief systems in O&P care
based on sound research or from expert opinion. The end goal of the conference is to publish a document that identifies and
ranks the available evidence and defines the current status of patient care. If possible, the group may develop consensus on
controversial issues and identify future research priorities.
The SSC on Prosthetic Foot/Ankle Mechanisms was called to examine the body of scientific evidence that supports the clinical prescription and use of prosthetic foot and ankle mechanisms. For purposes of simplicity and focus, “add-ons” such as torsion or vertical shock absorbers were excluded from emphasis and may be studied at a later time. Studies regarding foot/ankle components that included vertical shock or torsion absorption features as part of their mechanical design were included.

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The conference was developed around four key questions posed to the panelists:
Question 1: What scientific methods have been used to determine the functional performance of prosthetic feet and ankle
systems in current use?
Question 2: What is the correlation between the available scientific measurements and the clinical methods used to recommend
ankle/foot systems for specific amputees?
Question 3: What is the correlation between prosthetic foot/ankle systems and prosthetic outcomes (performance, patient
acceptance, durability, etc.)?
Question 4: In light of the literature review and the panel's discussion, what are the primary future research priorities?
Panelists reviewed the literature applicable to one or more of these questions, wrote papers on the subject, and presented
their perspectives to the group. All participants were asked to consider the relevance and validity of the following key areas:
Time-distance parameters as a measure of prosthetic performance
O2 consumption/energy consumption studies
Comparisons to normal gait and normal foot/ankle function
Comparisons to other prosthetic feet
Patient preference studies
Other methods used to evaluate or compare foot/ankle function
The topics of focus and contributors to the SSC on Prosthetic Foot/Ankle Mechanisms included the following:
Preface/Key Questions/Methods, Donald R. Cummings CP(LP), Susan Kapp, CPO(LPO)
Clinical Prescription and Use of Prosthetic Foot and Ankle Mechanisms: A Review of the Literature, Brian J. Hafner, PhD
Terminology in Prosthetic Foot Design and Evaluation, Nasreen F. Haideri, PhD
Perspectives on How and Why Feet are Prescribed, Gerry Stark, BSME, CP, FAAOP
Scientific Methods to Determine Functional Performance of Prosthetic Ankle-Foot Systems, Andrew H. Hansen, PhD
Clinical Perspectives on the Prescription of Prosthetic Foot/Ankle Mechanisms, Donald Shurr, CPO, PT
Clinical Perspectives on Prosthetic Foot/Ankle Designs, Terry J. Supan, CPO, FAAOP, FISPO
Research and Clinical Selection of Foot/Ankle Systems, Joseph M. Czerniecki, MD
The Functional Value of Prosthetic Foot/Ankle Systems to the Transtibial Amputee, Robert Gailey, PhD, PT
Perceptive Evaluation of Prosthetic Foot and Ankle Systems, Brian J. Hafner, PhD
Prosthetic Feet for Low Income Countries, John Craig, CPO
Future Trends in Prosthetic Foot/Ankle Research for Soldiers with Amputations, Joseph A. Miller CP, MS, 1st Lieutenant, Medical Services Corp, U.S. Army Reserves
As expected, some of the discussions were lively, and there were understandably areas of controversy, but the group
was able to arrive at agreement on the responses, which are summarized in the Proceedings on Prosthetic Foot/Ankle Mechanisms published in October 2005 and mailed to all Academy members.
The Academy continues to share and update the results through certificate programming, and an online course is under
development.
The Academy has developed a continuing education opportunity from the results of this SSC. Reading the following paper by Joseph M. Czerniecki, MD, titled "Research and Clinical Selection of Foot-Ankle Systems" and completing the quiz will earn you PCE credits. This quiz is available on the Paul E. Leimkuehler Online Learning Center (OLC). Simply read the paper, take the quiz, and earn ABC-approved PCE credits.
Joseph M. Czerniecki, MD
It is important to realize that the “recommendation of anklefoot systems for specific amputees” in today’s climate of evidence-based medicine would require that there is scientific evidence (a double-blind, placebo-controlled trial using
well-established and validated outcome measures) that shows enhanced function when a given component is provided compared
to other suitable components. No studies have been done that would meet this standard. This is supported by a systematic
review of the literature between 1966 and 2001 by van der Linde et al.1 Of the reviewed studies, only one achieved a methodological level of A, and only 15 achieved a methodological rating of B. The majority of these studies addressed outcome variables of metabolic oxygen consumption, stride kinematics, ground reaction forces, or more sophisticated joint movement and joint power output characteristics. These studies generally showed few significant differences between feet. Three B-level studies did show an increase in self-selected walking speed with different energy-storing feet compared to the solid ankle cushioned heel (SACH) foot. Additional studies showed that the increase in walking speed was accomplished by a greater stride length and reduced cadence. In addition to kinematic measures, three of nine B-level studies showed a reduction in metabolic oxygen consumption with the Flex or the Re-Flex VSP compared with the SACH foot.1
Hafner et al.2 suggest that one of the important factors that have limited the achievement of statistical significance in these biomechanical and metabolic studies is the small sample sizes. This review compiled all the results from multiple studies and showed that there may be some important trends that can be inferred even though each individual study was not able to show significance. The graphic display of the cumulative data from multiple studies is very illustrative of this feature.
Rietman et al.3 reviewed the literature between 1990–2000 related to “instrumented gait analysis” after amputation. This review concludes that gait analysis provides insight at the level of impairment but does not give insight at the level of disability or functional impairment. The authors conclude that gait analysis will continue to be of value in assessing the fundamental biomechanics of new prosthetic components, but further assessment of subjective perception and function in day-to-day tasks will be important.
A fundamental question needs to be asked at this point. Even if all of these studies showed “improvement” in an isolated
outcome variable such as self selected, stride length, ground-reaction forces, or metabolic oxygen consumption, would that have been adequate evidence to “recommend their use in specific amputees?” From a theoretical perspective the answer
would be no. What these studies would have demonstrated in a defined population, tested under specific laboratory conditions,
was that there was a beneficial effect. This does not mean that there would have been any perceived or quantifiable beneficial effect in real-world use. There are two relevant issues here: (1) Is the statistical difference of adequate magnitude to be clinically relevant?, and (2) Are the significant findings in the laboratory relevant to real-world mobility? Hofstad et al.4 use the term “ecological validity” from Mulder.5 An example of the first issue is that a drug may cause a statistically significant 10 percent reduction in cholesterol but have no effect on the development of clinical atherosclerosis. An example of the second issue is that the metabolic costs may be reduced while walking in linear constant-speed ambulation on a linoleum floor, but these conditions are rarely seen in day-to-day ambulation. Walking in real-world conditions with stopping, starting, inclines, and stairs may in fact result in increased metabolic oxygen consumption and have an adverse effect on functional mobility. These questions should not be interpreted as a rejection
of the need for fundamental biomechanical research. This research will be necessary to further understand the response of
the amputee to changes in design and to assist in the development of novel prosthetic designs.
Along with laboratory measurement, an additional approach used to quantify the effect of prosthetic feet is through subjective analysis. That is, amputees, through a variety of mechanisms, are asked to provide their subjective perceptions
or define, in a quantifiable way, their subjective impressions in various domains. Hafner et al.2 have reviewed the literature in this regard, and unfortunately, few studies have met adequate quality standards to be interpreted as to their relevance. In the systematic literature review of van der Linde et al.,1 only one level-A study and two level-B studies were acceptable. One showed no particular benefit of energy-storing feet over conventional feet, and the other two showed some benefit of the Flex-Foot® over the SACH foot; however, these studies were not conducted in a double-blind fashion. Blinding of subjects and investigators is clearly an essential part of studies that include a subjective evaluation.1,2,4
There is limited useful research to aid the clinician in the recommendation of specific foot-ankle mechanisms for specific
patients.
Interested in Submitting a Relevant Topic for Consideration for a State-of-the-Science Conference?
Topics for a State-of-the-Science Conference may be suggested by clinicians, educators, researchers, and other organizations associated with or engaged in the O&P profession. Final selection of a topic is made when agreement is reached by the Academy’s Planning Committee and with confirmation from the Academy Board of Directors.
Go to the Master Agenda page and review the conference guidelines.
Use the online topic suggestion form.
Topics should show the following:
a. Relevance to current clinical practice
b. Influence on a significant number of patients
c. Importance to improving patient outcomes
d. Controversy or lack of widespread consensus
e. Presence of gaps between knowledge and practice
f. Emerging or evolving concepts
g. Quantity and quality of available peer-reviewed literature
h. Degree of public interest
List three to six key questions to be specifically addressed about this topic.
a. Questions should address efficacy, risks, benefits, and clinical applications of this topic, as these questions will determine the scope and substance of the conference.
b. Questions should be straightforward and concise and framed so answers might be derived from scientific information and not based solely on subjective judgment or expert opinion.
The Academy will acknowledge receipt of all completed submittals and provide you with the Planning Committee’s recommendation or disposition. Unfortunately, not all topics will be approved or funded for a State-of-the-Science Conference. Approval of a specific topic does not ensure conference participation, as a national, multidisciplinary team of subject-matter experts will be developed by the conference chair and co-chair in collaboration with the Academy’s Planning Committee.
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Better Define Patient Needs
The majority of the research on prosthetic feet has classified the subject population with a fairly “coarse mesh.” That is, the populations have been defined on the basis of age, amputation level, and etiology of amputation. Part of the reason that the research on subjective evaluation of prosthetic components has been inconsistent is that the needs and priorities of subjects in these populations may be different. If we are going to get to the point where we can use scientific evidence to help in the prescription of the prosthetic feet, we must be able to more clearly define the needs, requirements, and priorities of individual patients so that we can better fit the prosthetic component to the patient.
There are a number of outcome tools available that measure the level of mobility of patients, such as the Medicare K levels, the Stanwood,6 the Locomotor Capability Index,7 or the Special Interest Group in Amputee Medicine (SIGAM)8 mobility grades. These are typically general mobility scales but do not allow one to measure, for instance, the intensity of mobility and the potential need for impact absorption or torsional activities that the patient might experience in his or her day-to-day functional tasks. For example, Medicare K levels divide the functional mobility status of the amputee into five levels, K0–K4, but they should not be used to prescribe a prosthetic foot. This is illustrated by the K2 level description:
“has the ability for ambulation with the ability to traverse low-level environmental barriers such as curbs, stairs, or uneven surfaces. Typical of the limited community ambulator.” Would you prescribe the same prosthetic foot to someone who
lived in an apartment in an urban environment and walked exclusively on level surfaces as you would to someone who lived in a doublewide mobile home in a rural environment with extensive irregular terrain, and also enjoyed fishing? The clinical history, in contrast, attempts to identify special patients’ needs and priorities when arriving at a prosthetic prescription. Unfortunately, as it is used in the clinical context, it cannot be quantified and used for scientific investigation.
The approach used by Postema et al.9 may provide the foundation for a needed future direction—the development of a tool that quantifies a patient’s mobility in key domains and also quantifies the importance of function within each of the domains for an individual patient. Postema et al.9 developed two questionnaires. The first questionnaire was an evaluation of the prosthetic foot measure that included 27 questions grouped into four separate domains. The amputee rates how well the prosthetic foot performed on a 0–10 scale for each question. The second questionnaire included 12 factors that
relate to prosthetic foot function. The subjects then were presented with 66 pairs of these 12 factors and were asked to
rank the importance of the factor of each presented pair.
These questionnaires allow you to define a patient’s needs and priorities in a more comprehensive way and then measure the effect of differences in prosthetic feet on their function. For example, if you were doing a research investigation on impact-absorbing pylons in transtibial amputees, you might find no beneficial effect with conventional subjective or objective biomechanical measures. But if you used the approach Postema et al.9 described, you might find that an impact-absorbing pylon benefited those who walked over irregular terrain or on inclines and who prioritized comfort as
an important criterion. This would then suggest that a clinician could administer a questionnaire at the time of clinic visits to assess the needs and priorities of a given patient and then provide a prosthetic foot that had been shown to be beneficial in that population.
Better Validated Tools for Evaluation and Measurement of Function That Have Adequate Sensitivity to Detect Change in Function Over Time As Well As Psychophysiologic Measures
Currently, the tools that are available to the investigator to measure the effect of prosthetic components on key functional
parameters are limited. We need measurement tools that have adequate sensitivity and specificity, adequate ability to detect
change in function over time, and adequate floor and ceiling characteristics for the population under study. For example,
some key domains that could be measured are perception of exertion, fatigue, mobility, and stability.
Development of Tools That Can be Used in Biomechanical or Metabolic Measurement During Real-World Functional Tasks
The majority of the scientific biomechanical research has been done in a laboratory and oftentimes walking on a treadmill.
This is inadequate to comprehensively quantify the effects of prosthetic feet on function. Equipment is available to accurately and reliably measure VO2 in the field. Techniques to measure impact transients, residual-limb torque, forces, and activity are needed. This should help better quantify the influence of prosthetic feet on function in a more “ecologically valid” way.
Prosthetic Foot Evolution and Rate of Production
The current practice of prosthetic foot development and introduction to the marketplace will pose significant challenges to the development and utilization of patient-specific criteria for prosthetic foot prescription. New prosthetic feet are being introduced regularly. These prosthetic feet are introduced without any published quantification of even their most basic functional characteristics. Any research done on evaluation and quantification of performance will always lag behind the marketplace. Although a long way from being a perfect solution, a key question that needs to be answered is whether or not it is possible to develop some simple instrumented quasi-static load deflection evaluations that all manufacturers will be required to perform on their prosthetic feet before bringing them to the marketplace, such as a heel-strike simulation, a forefoot keel dorsiflexion and release, and a medial and a lateral foot load to simulate the effect of walking on irregular terrain. These would allow some objective measurement that a clinician could understand so that new feet could be viewed in the context of feet available in the marketplace. So if a new foot was developed and its loading characteristics were quantified, you might be able to say, “It is better than a Seattle Lightfoot in absorbing energy at the heel but stores and returns less energy in the forefoot keel than a Renegade, and is about as stiff in the medial lateral plane as a LuXon® Max.” Ultimately new clinical studies would need to be done, but this could be used in the interim to help a clinician predict the utility of a foot for a patient with a given constellation of functional needs.
Time Delays in Funding, Conducting, and Publishing Research
Currently, the average time delay required to design and write a research proposal may span two to three months. Subsequently, there are additional delays from submission of the research grant through review, and, if successful, waiting for funding to arrive. After receipt of funding, depending on the study design, it will then take two to three additional years to complete the study. There will then be an additional 12- to 18-month delay before it is in print. Thus from inception to completion, five years may pass. This is incompatible with the rate of prosthetic foot development and testing. The use of modeling of different gait activities and the effect of foot design may ultimately allow the prediction of the effect of a novel foot without needing to conduct a three-year clinical trial. The development of these models will, of course, take time, and so will their validation.
Van der Linde H, Hofstad CJ, Geurts AC, et al. A systematic literature review of the effect of different prosthetic components on human functioning with a lower limb prosthesis. J Rehabil Res Dev 2004;41:555–570.
Hafner BJ, Sanders JE, Czerniecki J, Fergason J. Energy storage and return prostheses: does patient perception correlate with biomechanical analysis? Clin Biomech 2002;17:325–344.
Reitman JS, Postema K, Geertzen JHB. Gait analysis in prosthetics: opinions, ideas and conclusions. Prosthet Orthot Int 2002;26:50–57.
Hofstad C, Linde H, Limbeek J, Postema K. Prescription of prosthetic ankle-foot mechanisms after lower limb amputation. Cochrane Database Syst Rev 2004;(1):CD003978.
Mulder T, Hienhuis B, Pauwels J. Clinical gait analysis in a rehabilitation context: some controversial issues. Clin Rehabil 1998;12:99–106.
Hanspal RS, Fisher K. Assessment of cognitive and psychomotor function and rehabilitation of elder people with prostheses. BMJ 1991;302:940.
Franchignoni F, Orlandini D, Ferriero G, Moscato TA. Reliability, validity, and responsiveness of the locomotor capabilities index in adults with lower-limb amputation undergoing prosthetic training. Arch Phys Med Rehabil 2004;85:743–748.
Ryall NH, Eyres SB, Neumann VC, et al. The SIGAM mobility grades: a new population-specific measure for lower limb amputees. Disabil Rehabil 2003;25:833–844.
Postema K, Hermens HJ, de Vries J, et al. Energy storage and release of prosthetic feet Part 2: subjective ratings of 2 energy storing and 2 conventional feet, user choice of foot and deciding factor. Prosthet Orthot Int 1997;21:28–34.
Joseph M. Czerniecki, MD, is affiliated with the Department of Rehabilitation, University of Washington, Seattle, and VA Rehabilitation Research Center of Excellence, Limb Loss Prevention and Prosthetic Engineering, VAPSHCS, Seattle, Washington. Send correspondence to: Joseph M. Czerniecki, MD, Director RCS, VAPSHCS, 1660 S Columbian Way, Seattle, WA 98108; e-mail:
Editor’s Note: This article is an excerpt from State-of-the-Science Conference proceedings. The conference and original printing were made possible by an Academy grant from the U.S. Department of Education (H235J040017).
Take the quiz at the Academy's Online Learning Center.
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