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Section 2: Upper Limb
Figure 24
both body -powered and myoelec tric prostheses. A, Both sys tems allow full elbow range of m otion and retain forearm rotation. B, Elec tric hands provide greater grip f orce and a more natural appear­ance than voluntary-opening split hooks. This patient nds both sets of prostheses valuable and can match the most appropriate design with a particular activity.
transradial and wrist disarticulation lev­els. For the blind bilateral transradial amputee, sensation is required for func­tion. In these patients, surgical interven­tion (such as a Krukenberg procedure or a toe transfer to the forearm [Vilkki procedure]) is indicated to produce a limb with manipulative capabilities24 (Figure 25).
Photographs of a patient with bilateral wrist disarticulations who was tted with
useful dynamic positioning of the pros­thesis in space25 (Figure 26). Surgical lengthening using bone allograft, which allows for improved function resulting from a longer residual limb, has been beneficial for managing short trans­humeral amputations26 (Figu re 27).
As with a transradial prosthesis, in­dependent donning of the transhumeral prosthesis is a primary goal. Donning
Transhumeral Level
Body-powered systems appear to offer the best results for the patient with a bilateral transhumeral amputation. However, electric terminal devices and elbows provide greater forces and can be worn on the nondominant side to com­plement the function of a dominant side body-powered prosthesis. The ability to easily and securely position the pros­thesis in space becomes more critical as physiologic joints are lost. Positive lock­ing wrists and humeral rotators should be considered for these patients. Because of the loss of glenohumeral rotation in the transhumeral prosthesis, it may be beneficial for the surgeon to perform an angulation osteotomy to enhance the
independence is almost always achieved when body position control is used, but it may be compromised when myo­electric control is used because of the need for skin-to-electrode contact and the difficulty in donning these systems. In the experience of this chapter’s au­thor, nearly all bilateral arm amputees with one or both amputations at the transhumeral level prefer a body-pow­ered prosthesis on the transhumeral side that incorporates a four-function forearm set-up over myoelectric or other hybrid control options. Nevertheless, electric control of one or more components may be advantageous for some individuals if the requisite force and/or excursion for body-powered control are unavailable.
Figure 25
transradial amputee who underwent a Kruken­berg procedure on the left hand and a Vilkki procedure on th e right hand. These procedures provided the patient with sensate limbs with a variety of gripping options.
Photograph of a b lind, bilateral
New suspension/control systems, such as those with high consistency rubber silicone suction sockets with myoelectric interface capabilities4 and other electri­cally controlled input options under development, may necessitate the in­corporation of these newer technologies into bilateral fitting practice if they offer functional advantages for the user.
Shoulder Disarticulation
When fitting a patient with a bilateral shoulder disarticulation, it is advisable to start with as simple a prosthetic sys­tem as possible. Often, only the domi­nant side is fit initially. The complexity of the control system should be kept to a minimum, starting perhaps with only an activated terminal device and elbow. As the patient becomes familiar with the use of the prosthesis, wrist function can be added, followed by humeral rotation and a locking shoulder joint. The pros­thesis for the nondominant side can be fitted after the user has gained confi­dence in using the dominant-side pros­thesis. Complexity on the nondominant side can be staged in a similar fashion as used for the dominant-side prosthesis. In general, the dominant-side prosthesis
Atlas of Amputations and Limb Deciencies, Fourth Edition © 2016 American Academy of Orthopaedic Surgeons
312
Chapter 24: Bilateral Upper Limb Prostheses
Figure 26
al/shoulder disarticulation amputee who ben­eted from an angulation osteotomy on his right limb that facilitates physiologic humeral rotation, which improves rotational stability and provides added positioning control of the prosthesis.
Photograph of a transhumer-
of the bilateral pair is configured with mechanical, cable-actuated components (similar to the four-function set-up), whereas the nondominant-side pros­thesis incorporates either all-electric or hybrid components to provide comple­mentary functions.1 When possible, the electric prosthesis should use dedicated variable speed control of the prehensile device, the wrist, and the elbow.
Summary
Successful rehabilitation of a patient with a bilateral arm amputation is best achieved with a team approach. Bilater­al arm amputees, especially those with high-level loss, will benefit greatly from prosthetic intervention and other assis­tive technologies, including automobile modification, communication devices, self-care devices, and nonprosthetic manipulation devices that serve to aug­ment the functions of the user. Each bi­lateral arm amputee must be treated as a unique individual. The needs, goals, and desires of the individual should be the focus of the rehabilitation team. The fitting methods and philosophies pre­sented in this chapter should serve only
as a guide for successful prosthetic re­habilitation. Variations to this approach will be required based on the particular unique presentation of the individual being treated and his or her expressed preferences for particular prosthetic options.
Experience has shown that careful attention to socket fitting, ease of use of the control system, and minimized prosthesis weight are critical aspects in successful rehabilitation. Proven desir­able features of a successful prosthesis are comfort, aesthetics, feedback, don­ning independence, control reliability,
Figure 27
with bilateral transhumeral amputations who underwent surgical bone lengthening with allograft on his left limb to improve function by providing a longer lever to allow better prosthesis control and stability. A, Because the patient had a very short left residual limb, he was initially tted with a prosthesis only on his dominant right side. Photographs show the left limb after allograft transplantation (B) and a fter tting with bilateral body-powered prostheses (C).
Photographs of a patient
variable speed control, and locking joints. Clinical fitting protocol is driv­en by the availability of contemporary components and the control strategies for their operation. As new compo­nents and control schemes emerge, they should be objectively evaluated. New possibilities should be explored in the light of what is possible and should not be limited by what has previously been done. Despite the many shortcomings of state-of-the-art arm prostheses, bilateral amputees often make good use of these tools as they strive to achieve functional independence.
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Section 2: Upper Limb
References
1. Uellendahl JE, Heckathorne CW: Creative prosthetic solutions for the person with bilateral upper extremity amputations, in Atkins D, Meier R, eds: Functional Restoration of Adults
and Children With Upper Extremity Amputation. New York, NY, Demos
Medical Publishing, 2004, pp 225-237.
2. Uellendahl JE, Heelan JR: Prosthetic management of the upper limb de­cient child, in Alexander M, Molnar G, eds: Physical Medicine and Reha-
bilitation: State of the Art Reviews.
Philadelphia, PA, Hanley & Belfus, 2000; vol 14, no 2, p 232.
3. Malone JM, Fleming LL, Roberson J, et al: Immediate, early, and late post­surgical management of upper-limb amputation. J Rehabil Res Dev 1984;21(1):33-41. Medline
4. Uellendahl JE, Mandacina S, Ramdial S: Custom silicone sockets for myo­electric prostheses. J Prosthet Orthot 2006;18(2):35-40. DOI
5. Billock JN: e Northwestern Univer­sity supracondylar suspension tech­nique for below elbow amputations. Orthot Prosthet 1972;26(4):16 -23.
6. Sauter WF, Naumann S, Milner M: A three-quarter type below-elbow sock­et for myoelectric prostheses. Prosthet Orthot Int 1986;10(2):79-82. Medline
7. McLaurin CA, Sauter WF, Dolan CM, Hartmann GR: Fabrication procedures for the open-shoulder above-elbow socket. Artif Limbs 1969;13(2):46-54. Medline
8. Bush G: Powered Upper Extremity Prosthetics Programme: Above Elbow Fittings. Hugh MacMillan Rehabilita-
tion Centre, Rehabilitation Engineer­ing Department Annual Report.
1990;35-37.
9. Farnsworth T, Uellendahl J, Mikosz MJ, Miller L, Petersen B: Shoulder re­gion socket considerations. J Prosthet Orthot 2008;20(3):93-106. DOI
10. Uellendahl JE: Upper extremity myoelectric prosthetics. Phys Med Rehabil Clin N Am 2000;11(3):639-
652. Medline
11. Uellendahl J, Heckathorne C: Pros­thetic Component Control Schemes for Bilateral Above-Elbow Prostheses.
Proceedings of the Myoelectric Control Symposium, University of New Bruns­wick, 1993, pp 3-5.
12. Ivko JJ: Independence through humeral rotation in the convention­al transhumeral prosthetic design. J Prosthet Orthot 1999;11(1):20-22.
DOI
13. Heckathorne CW: Manipulation in unstructured environments: Ex­tended physiological proprioception, position control, and arm prosthe­ses. Proceedings of the International
Conference on Rehabilitation Robotics.
Piscataway, NJ, Institute of Electrical and Electronic Engineers, 1990, pp 25-40.
14. Childress DS: Control of limb prostheses, in Bowker JH, Michael JW, eds: Atlas of Limb Prosthetics:
Surgical, Prosthetic, and Rehabilita­tion Principles. St. Louis, Mosby-Year
Book, 1992, pp 175-198.
15. Simpson DC: e choice of control system for the multi-movement prosthesis: Extended physiological proprioception, in Herberts P, et al, eds: e Control of Upper Extremity Prostheses and Orthoses. Springeld, IL, Charles C omas Publishers, 1974, pp 146-150.
16. Doubler JA, Childress DS: Design and evaluation of a prosthesis control sys­tem based on the concept of extended physiological proprioception. J Reha- bil Res Dev 1984;21(1):19-31. Medline
17. Heckathorne C, Childress D, Grahn E, Strysik J, Uellendahl J: E.P.P. con­trol of an electric hand by exteriorized forearm tendons. Proceedings of the
Eighth World Congress of the Inter­national Society for Prosthetics and Orthotics, Brussels, Belgium, ISPO,
1995, p 101.
18. Heckathorne CW, Uellendahl J, Chil­dress DS: Application of a force-ac­tuated position-servo controller 8 for electric elbows. Proceedings of the
Seventh World Congress of the Inter­national Society for Prosthetics and Orthotics. Brussels, Belgium, ISPO,
1992, p 315.
19. Carlson L, Veatch B, Frey D: Ecien­cy of prosthetic cable and housing. J Prosthet Orthot 1995;7(3):96-99. DOI
20. Kuiken TA, Li G, Lock BA, et al: Targeted muscle reinnervation for real-time myoelectric control of multifunction articial arms. JAMA 2009;301(6):619-628. Medline DOI
21. Kuiken TA, Dumanian GA, Lipschutz RD, Miller LA, Stubbleeld KA: e use of targeted muscle reinnervation for improved myoelectric prosthesis control in a bilateral shoulder dis­articulation amputee. Prosthet Orthot Int 2004;28(3):245-253. Medline
22. Hudgins B, Parker P, Scott RN: A new strategy for multifunction myo­electric control. IEEE Trans Biomed Eng 1993;40(1):82-94. Medline DOI
23. Simon AM, Lock BA, Stubbleeld KA: Patient training for functional use of pattern recognition-con­trolled prostheses. J Prosthet Orthot 2012;24(2):56-64. Medline DOI
24. Vilkki SK: Free toe transfer to the forearm stump following wrist amputation: A current alternative to the Krukenberg operation]. Handchir Mikrochir Plast Chir 1985;17(2):92-97.
Medline
25. Marquardt E, Ne G: e angulation osteotomy of above-elbow stumps. Clin Orthop Relat Res 1974;104:232-
238. Medline DOI
26. Wilkins RM, Brown WC: Allogra transplantation to lengthen trans-hu­meral amputation limbs. Confer-
ence Proceedings of the 12th World Congress of International Society for Prosthetics and Orthotics. Brussels,
Belgium, ISPO, 2007, p 310.
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Chapter 25
Upper Limb Provisional Prostheses
Chris Lake, L/CPO, FAAOP
Abstract
Although it is not a new concept, the regular and thoughtful use of provisional prostheses (also described as trial and preparatory prostheses) can enhance meaningful prosthetic use, reduce the likelihood of rejection, and place the individual with an upper limb ampu­tation in the center of the prosthetic care model. e information gleaned from the tting stage presents a clearer prediction of the eventual prosthetic outcome. e expanding and increasingly complex choices of prosthetic components coupled with the increased desire by third-party payers for assurances that the recommended course of treatment will be successful have made provisional ttings increasingly more important. e provisional tting can form the basis for a case-specic outcome-based protocol that will provide that evidence.
Keywords: improved clinical upper limb prosthetic outcomes; preparatory upper limb prosthesis; provisional prosthesis; trial upper limb prosthesis; upper limb amputee
Introduction
Powerful clinical tools are available to the prosthetist. Although it is not a new concept, regular and thoughtful use of one of these tools–provisional pros­theses–can enhance meaningful use of prosthetic devices, reduce the likeli­hood of rejection, and place the individ­ual with an upper limb amputation in the center of the care model. The fitting stages of the provisional prosthesis allow the prosthetist to verify that the correct course of treatment is being pursued to provide optimal care for a given patient. The information gleaned through these processes creates a clearer prediction of the eventual prosthetic outcome.
Terminology
The term provisional prosthesis has variable applications. In some instanc­es, it is synonymous with a prepara­tory prosthesis, a prosthesis designed to withstand early prosthetic endeavors
Mr. Lake serves as an unpaid consultant to Innite Biomedical Technologies, Liberating Technol­ogies, Ottobock, Ripple, and ToughWare Prosthetics.
for an extended period of time while al­lowing the prosthetist to closely monitor the maturation process of the residual limb.1 In this preparatory phase, a pro­visional prosthesis allows verification and fine-tuning of prosthetic recom­mendations and increases the likeli­hood of a successful outcome through a patient-centered approach, consistent prosthetic attention, and adaptations to long-term residual limb response that can result in a better and more com­fortable fit.
Alternatively, the same term can be applied to a trial prosthesis, which is intended to allow testing of the perfor­mance, qualities, and/or suitability of a specific prosthetic design and/or com­ponent for an individual with a legacy upper limb amputation.2 In this appli­cation, a provisional prosthesis used in the early stages of a new course of pros­thetic management can provide case­specific evidence to support or dispute
a particular prosthetic recommenda­tion and can be a strong predictor of longer-term outcomes. The information provided can help members of the reha­bilitation team, including the referring physician, prosthetist, and therapist, to meaningfully and productively adjust the course of prosthetic management at an early point in the process.
Whether used during the early pre­paratory phase of prosthetic rehabilita­tion or as a diagnostic trial device when exploring a new prosthetic design vari­ation, provisional prostheses determine an individual’s general candidacy for a definitive upper limb prosthesis, serve as case-specific evidence to evaluate prosthetic recommendations, and pro­vide evidence-based support to justify third-party payer authorization of the expenses associated with definitive prosthetic care.
Rationale
The use of provisional prostheses in lower limb prosthetic management dates back to the 1930s.3 In contrast, the use of upper limb provisional prostheses is more recent, with the bulk of the litera­ture emerging in the late 1980s and ear­ly 1990s. of upper limb prostheses is challenging, requiring an analysis of the suitability of the device in vocational requirements, avocational interests, familial relation­ships, and basic activities of daily living. The elements of a satisfactory outcome are unique for every individual and de­pend on attaining a complex array of upper limb functions and appearances. As such, a thorough assessment of the prosthesis may require usage outside of the prosthetic facility in the user’s native
1,2,4
The functional assessment
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Section 2: Upper Limb
Tab le 1
environment. Provisional prostheses fa­cilitate this type of assessment.
the quality of upper limb prosthetic care by helping to generate objective and quantifiable information that leads to case-specific, evidence-based recom­mendations.5 A trial fitting is a practi­cal alternative in assessing intangible
Critical Elements of Patient-centered Upper Limb Prosthetic Care
Element Considerations
Fitting the prosthesis The prosthesis is ne-tuned throughout the process. The
Follow-up care This care is performed at least weekly throughout the
Repair and maintenance During the provisional phase, routine prosthesis main-
Information acquisition/
training
Information provided During the provisional phase, the patient is provided with
Use of multiple
prostheses
Setting the level of
patient expectations
Providing profes sional
knowledge and experience
denitive device is not delivered until optimal socket interface, component selection, and alignment have been determined.
process. The patient is a key collaborator and learns to identify events and sensations that signal the need for evaluation. Progress is assessed during follow-up care, and prosthetic recommendations may be modied or completely changed.
tenance and repair can be discussed. For example, the patient may learn how to lubricate and clean a terminal device.
The occupational therapy aspect of provisional manage-
ment provides the patient with the opportunity to train on the use of new devices as they are delivered and to identify and treat both sound and aected limb issues as they occur.
information on prosthetic technology and the available prosthetic options. Rejection of a prosthesis is less likely if the patient has the opportunity to assess dierent types of components, designs, and socket interfaces throughout the process.
Provisional ttings allow the use of multiple prosthetic
options so that the patient can assess and determine which prosthesis, terminal device, and/or design is best suited to specic activities.
A patient may have unrealistic expectations regarding an
upper limb prosthesis. The provisional management phase allows the clinician to continually assess and set realistic expectations. The prosthetics course can be adjusted to accommodate feasible expectations, and a psychologist and/or counselors can help the patient cope with unrealistic prosthetic goals.
The prosthetist and therapist should have a good, com-
prehensive knowledge of all the elements of prosthetic management. Continued training and education on related topics will allow the healthcare team to provide the patient with the best available prosthetic options and adjust the provisional management phase as needed.
variables such as patient motivation, body image, and expectations. Mea-
Provisional prostheses can improve
surable criteria, including skin con­dition, weight tolerance, upper limb strength, and the signal strength of targeted remnant muscles, also can be assessed. These and other variables are better assessed when the user/patient can actually experience the benefits and
drawbacks of a prosthesis rather than speculating about its value.4 Provisional fittings can help determine the optimal prosthetic solutions for an individual amputee through the assessment of var­ious components. As the residual limb matures, the transparent socket-frame interface of a provisional fitting gives clinicians a clear view of the evolving dynamics of the limb-prosthesis in­terface; thus, meaningful and effective adjustments are easier to accomplish at an earlier stage.2 Planning and fitting a provisional prosthesis also make the user the focus of a patient-centered ap­proach, with his or her values and needs integrated into the process
6-9
(Table 1). The likelihood of clinical success in­creases when users are actively involved in decision-making processes.10 Meier and Atkins11 emphasized the necessity of allowing amputees to make decisions regarding their lives and needs.
Clinical Application
Although the early course of provisional prosthetic care focuses on determining the general candidacy of the patient for upper limb prosthetic management, subsequent adjustments and prosthe­ses focus on ensuring continued success while carefully monitoring the patient as his or her residual limb matures and/or responds to prosthetic care. During these processes, patients are able to evaluate and determine the most ap­propriate components to address their specific needs. In addition, the pros­thetist can address the immediate soft­tissue response as edema subsides in the residual limb. As usage continues, the customary long-term tissue response of overall residual limb atrophy with re­gional muscle hypertrophy and global edema reduction may require repeated adjustments of the prosthesis to allow uninterrupted function. Electrodes, for example, may need to be relocated as the remnant muscles become more condi­tioned to prosthetic use. Similarly, ad­justments to the prosthetic suspension
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Chapter 25: Upper Limb Provisional Prostheses
Figure 1
prosthesis with exible inner sockets and ber­glass casting tape frames. Heavy-duty mailing tubes help provide support for the casting process.
Photograph of a provisional
system are frequently indicated. The adaptable design considerations that characterize these fittings reduce the lag time between fit issues and appropriate adjustments. This creates a state of flow between the patient and the clinician and can engender energy and excite­ment about the gains being made while fostering a deeper patient commitment to the prosthetic course of treatment.
Fitting and Component Considerations
The components used for provisional prostheses are generally the same as those used in definitive prosthetic man­agement. In trial applications, some of these components may be rented (for long-term assessment) or loaned (for short-term or in-office trials) from various manufacturers. In preparatory applications, components are generally definitively obtained. Most importantly, a provisional prosthesis must be ad­justable so that the clinician can keep pace with the changes of the dynamic residual limb. Thus, provisional and definitive prostheses may differ in con­struction techniques and preparation of components.
Figure 2
use require transparent thermoplastics. Inner sockets and outer frames can be fabricated with tra­ditional fabrication procedures. Photograph of a transparent provisional prosthesis.
Given the expeditious nature of pro­visional fittings, the use of flexible ther­moplastics for inner sockets is generally preferred. For temporary applications, alignment can be approximated using
The need for visual inspection associated with provisional prostheses for long-term
positive model throughout the fabrica­tion process is questionable, a bivalve thermoplastic duplication should be made, preferably of clear check socket
material (Figure 5). heavy-duty cardboard tubing, which is then covered by fiberglass casting tape (Figure 1). The patient’s skin and surroundings are protected from the rough finish of the fiberglass by apply­ing a self-adhering, thin, elastic support wrap to the outside of the provisional device. Fiberglass casting tape usually suffices for trial frames because of the expected short-term duration of use. In contrast, some provisional prostheses need to provide long-term ease in ad­justment and inspection. For this role, transparent thermoplastic is a better
Alignment and Residual
Limb Considerations
Provisional fittings have many benefits,
with alignment of the prosthesis and re-
sidual limb response being the most ev-
ident. Alignment includes not only the
angle at which a terminal device or other
components are oriented in relationship
to the socket but also the placement of
the components and features through-
out the prosthetic space. Alignment and
residual limb considerations are relevant
in all types of prostheses. frame material (Figure 2).
Provisional prostheses should be eas­ily adjustable without affecting the con­tinuity of prosthetic usage. The socket interfaces and frames should be adjusted and/or re-formed on site so the patient has continued access to prosthesis use. This is accomplished by forming inner sockets from materials that can be re­formed on modified models (Figure 3). When necessary, frames and some in­ner sockets can be drape molded with a nonadhering seam that allows them to be spread open on the model for easy removal and reapplication (Figure 4). This technique also maintains the orig­inal model of the socket interface and/ or frame so the clinician can go back to the original model and make changes as appropriate. If preservation of the
Passive Prostheses
The provisional passive prosthesis helps define the placement and specifications of component alignment as well as the length of the prosthesis. Many times, an individual who requests a passive pros­thesis is sensitive to prosthetic weight. With a provisional prosthesis, the length and the alignment angle can be inves­tigated and fine-tuned before defini­tive fabrication to provide the lightest perceived weight. Also, the pronation/ supination angle can be more readily defined. For individuals who will not be using a friction- or flexible-type of wrist unit, this particular rotational alignment is critical. With a proper pronation/ supination angle, the passive prosthesis evolves from a device that is
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Section 2: Upper Limb
Figure 3
modied is indicated by the circle. B, The positive model is reduced as appropriate. C, The test socket is placed back on the model and the rectied area (circle) is inspected. D, The test socket is heated in the area that will be re-formed. Baby powder is sprinkled on the heated plastic to keep the thermoforming nylon and vacuum bag from melting and/or sticking to the hot plastic. E, Thermoforming nylon is placed over the model and tied o to inuence a vacuum over the entire model. F, A vacuum bag is placed over the positive model and tied o accordingly. G, The vacuum bag is pulled on the model and the model is allowed to cool appropriately. H, The vacuum bag and nylon are removed and the modied area (circle) is inspected to verify that the desired results have been achieved.
Photographs demonstrating remodeling of exible inner sockets. A, The test socket is placed on the positive model. The area to be
aesthetic in nature to one that is a func­tional assistive tool for the individual’s sound-side arm.
Body-Powered Prostheses
The fitting of a provisional body­powered prosthesis will allow evalu­ation of long-term tissue loading with terminal device actuation. As an indi­vidual uses a body-powered prosthesis,
Figure 4
the protective lm remains on the material when heating, the material is not welded together. Photograph of a f rame that can be spread op en on a model to allow eas y removal and reapplicati on.
Inner socket and frames can be drape molded with a nonadhering seam. Because
his or her residual limb will adapt to these forces. As tissues in the middle and proximal parts of the residual limb begin to atrophy under loading, more pressure will be realized at the distal end. A translucent, provisional prosthe­sis allows observation and adjustment of these tissue changes in a precise and efficient manner.
This stage of prosthetic management also permits a thorough investigation of different cable routing methods and reaction forces and helps to ensure the most energy-efficient and biome-
Figure 5
sheets of clear check socket material around a positive model. Because the protective lm remains on the material when heating, the two sections are removable and not welded together.
Photograph of a bivalve thermoplastic duplication made by thermoforming two
chanically stable transition to a de­finitive body-powered prosthesis. In addition, the location and orientation of
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318
mechanical release levers, such as those encountered in quick-disconnect wrist units and remote elbow and shoulder locking mechanisms, can be refined to the user’s preferences. Segment lengths and mechanical joint positions and alignments also can be experienced and refined during the provisional stage.
Externally Powered Provisional Prostheses
Provisional fitting of an externally powered prosthesis provides benefits in component selection, alignment, and placement. These aspects set the starting point for the functionality and perceived weight of the prosthesis. An extended course of use with a provi­sional prosthesis also allows the clini­cian to monitor the muscular changes and soft-tissue responses in the residual limb. The prosthetic socket acts as the foundation of the prosthesis and can be undermined by residual limb atrophy and/or hypertrophic muscular response. The dynamic residual limb by its na­ture requires continued adjustment of the more static socket. The clinician should expect this interplay between the evolving human limb and the ad­justable man-made interface to continue for an extended time. For best results, this intensive adjustment stage should be maintained until the patient’s resid­ual limb size has remained stable with continued use of the prosthesis.
The clinician also should be obser­vant of electrode positioning. As the re­sidual limb matures with myoelectric prosthesis use, the residual muscle be­comes more toned, and optimal myosite positioning can change. Over time, the patient should become more adept at maintaining myosignals, and the re­sidual muscles will likely strengthen at different rates. The patient should be educated on how the prosthesis should react so that he or she can identify my­osite imbalance and the need for ad­justments. Educating patients provides them with confidence and a feeling of
Chapter 25: Upper Limb Provisional Prostheses
Figure 6
Photographs of t ask-specic upper lim b provisional (A) and deni tive (B) prostheses.
control. Along with electrode position and contact, the location of any addi­tional electrical switches can be refined as needed. As with body-powered de vices, segment lengths and mechanical joint positions and alignments can be experienced and refined during the pro­visional stage.
Hybrid Provisional Prostheses
The fitting of a provisional prosthesis is of particular value with hybrid pros­theses. Most hybrid prostheses combine a body-powered elbow with an exter­nally powered hand (and sometimes an externally powered wrist); there­fore, provisional fittings can offer sev­eral unique benefits. For example, the clinician can make better decisions re­garding placement of the battery and the charging hardware. Placing this hard­ware proximal to the elbow will lower the perceived weight of the prosthesis. This perceived weight can be further reduced by positioning the elbow joint more proximally.
A provisional prosthesis also allows patients to experience the nuances of different component placements so they
-
can decide what is best for their particu­lar circumstances. For example, placing the elbow joint in a slightly more supe­rior position than the anatomic elbow joint on the sound side will usually re­sult in more natural bilateral function in a seated position. The carrying angle of the elbow and flexion-extension an­gle of the prosthesis are also considered during this phase.
Task-Specific Provisional Prostheses
As the name implies, a task-specific pro­visional prosthesis has a very defined design and provides the opportunity to assess different designs for individ­ualized tasks such as swimming, par­ticipating in specific sports (such as basketball or golf), and customized vocational applications. For example, a task-specific provisional prosthe­sis was fabricated for a patient with a
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Section 2: Upper Limb
Figure 7
or have a built-in adapter (third device from the left). The two devices on the lef t were used for the patient in Figure 6. The Quick Disconnect Myo-Electric Wrist Adapter (Texas Assistive Devices) is shown in the fore ground. These t ypes of adapters pe rmit assessment of multip le prosthetic options through a common i nterface-fram e assembly, and they essentially allow a p rovisional prosthesis to function as several separate devices.
partial hand amputation that entailed resection of digits two, three, four, and five at the proximal metacarpal region and preservation of an intact thumb with very limited motion (Figure 6). To return to work as a tank fabricator, the patient had to be capable of safely handling large sheets of metal and op­erating hydraulic presses to shape the metal. Through the defined provisional stage, a prosthesis was created with a quick- disconnect wrist that attached to a voluntary opening hook with adjust­able tension and a range of common and job-specific tools (Figure 7). Although the patient’s thumb had limited motion,
Photograph of terminal devices that can be used with a quick-disconnect adapter
sound-side influence, electromyograph­ic strength and endurance, and weight tolerance, cannot be accurately assessed without the individual’s experience and practical use of the recommended pros­thetic designs.
Upper limb prosthetic management can occur as a process with several phases that allows assessments and revisions to the recommended pros­thetic course. Changes should be made in provisional prostheses based on the patient’s feedback and experiences to ensure that the definitive prosthesis will provide a good outcome that combines comfort, ease of use, and function.
he was able to generate approximately 2 pounds of pinch force against a well-positioned opposition post. This feature allowed him to handle paper­work and perform other fine pinch tasks in which his limited thumb force and sensation were still beneficial.
Summary
An individual’s meaningful use of a prosthesis can be enhanced with an ac­curately executed course of provisional prosthetic management. Variables, in-
References
1. Supan TJ: Transparent prepara­tory prostheses for upper limb amputations. Clin Prosthet Orthot 1987;11(1):45-48.
2. Sears HH, Andrew JT, Jacobsen SC: Experience with the Utah arm, hand, and terminal device, in Atkins DJ, Meier RH III, eds: Comprehensive
Management of the Upper Limb Amputee. New York, NY, Springer-
Verlag, 1989, pp 194-209. DOI
cluding patient motivation, body image,
3. Sullivan JE: e aer-care of ampu­tation stumps. Surg Clin North Am 1938;18:433-440.
4. Sears HH: Approaches to prescrip­tion of body-powered and myo­electric prostheses. Phys Med Rehabil Clin N Am 1991;2(2):361-371.
5. Brenner CD, Brenner JK: e use of preparator y/evaluation/training pros­theses in developing evidence-based practice in upper limb prosthetics. J Prosthet Orthot 2008;20(3):70-82.
DOI
6. Biddiss E, Chau T: Upper-limb prosthetics: Critical factors in device abandonment. Am J Phys Med Rehabil 2007;86(12):977-987.
Medline DOI
7. Meier RH, Esquenazi A: Prosthetic prescription, in Meier RH, Atkins DJ, eds: Functional Restoration of Adults
and Children With Upper Extrem­ity Amputation. New York, NY,
Demos Medical Publishing, 2004, pp 159-164.
8. Soltanian H, de Bese G, Beasley RW: Passive hand prostheses. Hand Clin 2003;19(1):177-183. Medline DOI
9. Michael JW: Externally powered prostheses for the adult transradial and wrist disarticulation amputee, in Meier RH, Atkins DJ, eds: Functional
Restoration of Adults and Children With Upper Extremity Amputation.
New York, NY, Demos Medical Pub­lishing, 2004, pp 187-197.
10. Meier RH, Esquenazi A: Rehabilita­tion planning for the upper extremity amputee, in Meier RH, Atkins DJ, eds: Functional Restoration of Adults
and Children With Upper Extremity Amputation. New York, NY, Demos
Medical Publishing, 2004, pp 55-61.
11. Meier RH, Atkins DJ: Postoperative and preprosthetic preparation, in Meier RH, Atkins DJ, eds: Functional
Restoration of Adults and Children With Upper Extremity Amputation.
New York, NY, Demos Medical Pub­lishing, 2004, pp 135-138.
Atlas of Amputations and Limb Deciencies, Fourth Edition © 2016 American Academy of Orthopaedic Surgeons
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Chapter 26
Silicone Interface Options in Upper Limb Prostheses
Elaine N. Uellendahl, BA, CP
Abstract
High consistency rubber silicone as an upper limb socket material is benecial for use at all amputation levels. is material increases comfort, provides auxiliary suspension through suction, and improves range of motion because of its elasticity.
Keywords: high consistency rubber silicone; interface; prosthetic socket; silicone
Introduction
Silicone is a synthetic chemical com­pound made from the commonly oc­curring element silicon. It has been used as an interface material in prosthetic sockets for the past several decades. The material characteristics of silicone are conducive to optimal outcomes, in­cluding its high tensile strength, low compression set (ability to return to its original shape after being compressed for a period of time), and high tear resis­tance.1 Silicone offers good biocompat­ibility and is characterized as nontoxic and biologically inert. In addition, sili­cone does not support bacterial or fun­gal growth.
In the field of prosthetics, the most traditionally familiar use of silicone as an interface material is the manufacture of roll-on liners. Such liners are gener­ally made using liquid silicone rubber. Another type of silicone, high consis­tency rubber (HCR) silicone, is used as a socket material.
Unique among materials routinely used for prosthetic interfaces, silicone is an elastic material that can be stretched to several times its size and still return to its original dimension. Elasticity coupled with flexibility help improve
Ms. Uellendahl or an immediate family member is a paid employee of New Touch Prosthetics and has stock or stock options held in New Touch Prosthetics.
1
range of motion and reduce edge pres­sure, resulting in greater comfort and functionality for patients. This improves functional outcomes by allowing a pa­tient to wear his or her prosthesis for longer periods and with greater comfort and increased range of motion.
2
High Consistency Rubber Silicone
Fabrication Processes and Variants
HCR silicone interfaces are made by applying uncured silicone, a clay-like material, to a dehydrated plaster model. The HCR silicone is prepared by add­ing an appropriate percentage of catalyst and/or inhibitor. Although HCR silicone check sockets are typically unpigmented and remain transparent for diagnostic fittings, definitive sockets can have cus­tom pigmentation to match the patient’s skin or another desired color. A two-roll mill is used to mix the ingredients and make a sheet of silicone (Figure 1). The thickness of the silicone is controlled with the bite or spacing between the rollers. Successive layers of silicone can be added between sequential periods of oven curing to create channels for wires, to embed electrodes, or for the applica­tion of zippers. The shore, or hardness,
Figure 1
used to mix the components of silicone and control the thickness.
of silicone can be used to vary the elas­ticity of a socket, with a midshore sili­cone most often used. Because silicone interfaces that have lower, more elastic shores do not retain their shape as well as those with higher shores and have decreased tear strength, silicone mate­rials with lower shore measurements are usually applied only in selected areas.
In addition to the comfort properties of silicone, another crucial advantage of the material is its versatility in design. If the patient has a residual limb with a bulbous distal end, a zipper can be added in the silicone interface to aid in donning and doffing the prosthesis.3 Anchors can be embedded to attach to supportive frames or straps. The thick­ness of the silicone can be selectively varied, and gel pads can be sandwiched between layers of silicone to provide additional padding and protection for especially sensitive or scarred areas. In an electronic prosthesis, necessary
Photograph of a two-roll mill
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