Evaluation of Titanium Ultralight Manual Wheelchairs Using Ansi/resna Standards.

INTRODUCTION Choice of a suitable wheelchair requires serious consideration. The U.S. Food and Drug Administration recommends testing wheelchairs using American National Standards Institute (ANSI)/Rehabilitation Engineering and Assistive Technology Society of North America (RESNA) testing standards to assess performance and safety and estimate life expectancy of a wheelchair. Results from ANSI/RESNA standard tests are a source of information about technical quality and performance and allow comparison of results across devices. The content of the standard tests covers many aspects that affect wheelchair usage and selection, such as dimensions, static stability, braking effectiveness, strength, and durability.

Dimensions, weight, and turning radius clue consumers in to whether a wheelchair will fit in their homes, working environments, and transportation means. Wheelchair performance in the static stability tests reveals the estimated behavior of the wheelchair on an incline.

The results indicate how the stability of the wheelchair is affected by adjustment of the axle and other components. Determining wheelchair strength and durability from retail advertisements and user manuals is difficult. Although medical insurers' prescription guidelines typically require 3 to 5 years before a replacement wheelchair will be covered, previous research has shown that the predicted life expectancy of some wheelchairs is significantly less -. Premature wheelchair failure could potentially injure the users and may require them to pay for replacements, which can cost several thousand dollars. According to Smith et al., wheelchair users expect wheelchairs to improve their quality of life and help them maintain or achieve a desired level of mobility . Users expect their wheelchairs to be comfortable, easy to propel, safe, and attractive . In a survey of wheelchair users with amyotrophic lateral sclerosis, the most desirable features of manual wheelchairs were a lightweight frame and a small turning radius .

Comfortable propulsion and support, light weight, and small dimensions are very important features, especially for active manual wheelchair users -. A lighter wheelchair has lower rolling resistance, which reduces the force required to propel it. Thus, lighter wheelchairs are suggested for preserving upper-limb function of manual wheelchair users . Developing a lighter and more functional wheelchair is a goal for the design of many manual wheelchairs. The titanium wheelchair is a product in response to this goal.

ANSI/RESNA standard tests provide specific testing protocols to evaluate the performance and durability of wheelchairs and serve as a universal platform for data collection and comparison. Reports using ANSI/RESNA standards evaluated aluminum ultralight and steel lightweight wheelchairs. Ultralight wheelchairs lasted more than five times as long as lightweight wheelchairs before failures occurred during fatigue tests -. However, ultralight wheelchairs experienced more repairable component failures, such as bolt or caster-stem failures and screws loosening. Although repairable component failures do not damage frame integrity, multiple component failures require frequent maintenance and may place the user in hazardous situations.

Many ultralight wheelchairs have titanium frames and/or components.

Since titanium has a higher strength-to-weight ratio than aluminum, if engineered correctly, it could preserve the strength of the wheelchair frame while lowering the weight. Conventional wisdom in our wheelchair clinic has been that people who use titanium chairs benefit from their highly durable and lightweight properties, although no standards testing results of titanium wheelchairs have been reported in the literature.

Our goal in this study, similar to prior works in this area, was to test a series of commercially available titanium rigid-frame wheelchairs using ANSI/RESNA testing procedures. The standard test to determine braking effectiveness according to the International Organization for Standardization (ISO) was also incorporated in this study , since no braking effectiveness test for manual wheelchairs is included in the current version of the ANSI/RESNA standards. We hypothesized that these titanium wheelchairs would be in compliance with ANSI/ RESNA standards and that they would be more durable than previously tested aluminum ultralight and lightweight wheelchairs.

METHODS Study Wheelchairs Twelve titanium rigid-frame wheelchairs representing four models from three manufacturers were tested using ANSI/RESNA wheelchair standard tests: the Invacare Top End (Invacare; Elyria, Ohio), the Invacare A4, the Quickie Ti (Sunrise Medical; Longmont, Colorado), and the TiLite ZRA (TiLite; Kennewick, Washington) (Figure 1). They were the most popular titanium ultralight rigid-frame wheelchairs prescribed at the Center for Assistive Technology at the University of Pittsburgh Medical Center. They were ordered with the same seat dimension specifications and standard components. Because of the cost and time to test wheelchairs, we only tested three wheelchairs of each model.

Standards Testing Procedure We completed the whole battery of ANSI/RESNA manual wheelchair standard tests and assessed braking effectiveness using the ISO standard test. This article focuses on the test results of static stability; braking effectiveness; and static, impact, and fatigue strength tests.

The dummy used in this study was built according to the requirements of ANSI/RESNA standards.

[FIGURE 1 OMITTED] Static Stability The wheelchairs were tested in their most and least stable configurations (forward and rearward directions) in the static stability tests ([section]1 in the ANSI/RESNA wheelchair standards). A 100 kg dummy was loaded into the test wheelchair. The wheelchair was secured on a platform using straps that did not interfere with tipping movement. An engineer increased the platform angle slowly and recorded the angle at which the front casters lifted from the platform just enough for a piece of paper to pass between the casters and platform. In the rearward stability tests, the rear wheels were locked with parking brakes or by securing the wheels with straps that limited the rolling motion of the wheels relative to the frame. In the other portions of the static stability tests, blocks or brackets that did not impede the rolling motion of the wheels were used to stop the wheelchair from rolling downhill.

We placed the wheelchair in its least stable position in the rearward direction by moving the rear-wheel axle forward, reclining the backrest backward, and increasing the front seat height by adjusting the caster position. We positioned the wheelchair in the extreme least stable position, since no indication or limitation for the range of the rear-wheel axle position was noted on the wheelchairs or in the user manuals. Most of the wheelchairs in their least stable setting tipped backward on a horizontal plane with the dummy loaded. Although these extremely unstable positions in the rearward direction were not realistic wheelchair settings, we still proceeded and recorded the tests because the purpose of having the standardized tests is to reveal the actual properties of the wheelchair. To address this limitation, we modified the testing procedure by placing the wheelchair facing downhill on the platform and securing it with straps to prevent it from tipping over completely (Figure 2(a)). The slope was then increased, and the angle at which the front casters touched the platform was recorded (Figure 2(b)). The reading was a negative number.

Braking Effectiveness In the braking effectiveness tests ([section]3 in the ISO wheelchair standards), we kept the wheelchairs in the same setting as when they came out of the box (the axle was in the most rearward setting), loaded them with a 100 kg dummy, and engaged the rear brakes.

The tests were performed on the same platform as the static stability tests. While increasing the slope of the platform, we recorded the angle at which the wheelchair started to slide downhill. The wheelchair was tested in its forward and rearward orientations. Since the steepest slope that fulfills the requirement of the Americans with Disabilities Act (ADA) is 7[degrees] (1:8), with a maximum rise of 75 mm (3 in.) for existing buildings and facilities, we expected the wheelchair to be able to stay stationary on a 7[degrees] slope.

Static, Impact, and Fatigue Strength Tests (Durability Testing) Static, impact, and fatigue strength tests ([section]8 in the ANSI/RESNA wheelchair standards) evaluate the strength of the wheelchair structure by applying different types of loads on specific components. A pneumatic ram was used to apply static force to the footrest, armrests, and tipping levers (if present) according to the standard. Impact force was applied using a pendulum on several components of the wheelchair (footrest, caster wheels, pushrim) that are prone to impacting objects.

Any permanent deformation or component failure was considered a failure as denoted in the standards.

Fatigue strength was evaluated by the double-drum and curb-drop tests (DDT and CDT, respectively). Each wheelchair was loaded with a 100 kg dummy during the tests. In the DDT, the position of the drive wheels was set at the midaxle position according to the requirements in the standards. Because the titanium wheelchairs were unstable in this position, we set the rear axles in the most rearward position horizontally and the midposition vertically (which was how they arrived from the suppliers). Other wheelchair settings were set according to the requirements in the standard. The leg length of the dummy was adjusted to fit the wheelchair dimensions, and the feet were fixed on the footrests. The dummy's trunk and legs were secured to the wheelchair, although hip-joint motion was preserved through a spring-loaded damper system that allowed physiological-like motion during the testing. According to the standard, the dummy was positioned centrally on the seat. Generally, the weight of both legs is 32 percent of total body weight . Individuals who are 6 months post spinal cord injury may lose 15 to 46 percent of their lower-limb muscle area .

We carefully kept the weight-loading on the front casters within 20 to 25 percent of the total weight of the dummy and the wheelchair to approximate the influence of the occupant's body weight and the weight of the wheelchair and prevent overloading on the casters by adjusting the location of the dummy either in an anterior or posterior direction. The 12 mm-high slats on the drum simulate sidewalk cracks, door thresholds, potholes, and other small obstacles on the rolling surface. Two clamps attached to the rear-wheel axle held the position and balance of the wheelchair on the double-drum machine but allowed vertical movement without appreciable sideward drift (Figure 3). The rear drum runs at a speed of 1 m/s, and the front drum turns 7 percent faster to vary the frequency with which the front and rear wheels encounter the slats. A wheelchair that completed 200,000 cycles on the test machine was considered to have passed the DDT.

[FIGURE 2 OMITTED] Only the wheelchairs that passed the DDT continued on to the CDT.

In the CDT, the wheelchair was repeatedly dropped freely from a 5 cm height onto a concrete floor to simulate going down small curbs. A wheelchair passes the wheelchair standard tests when it survives 200,000 cycles in the DDT and 6,666 cycles in the CDT without harmful damage . The intensity of the fatigue tests mimics 3 to 5 years of daily use . We repeated the fatigue tests until each wheelchair had permanent damage to determine the exact survival life. For the purpose of comparing fatigue life, we used the following formula to compute the number of equivalent cycles (ECs) ,6-:

Total ECs = (DDT cycles) 30 x (CDT cycles). (1) [FIGURE 3 OMITTED] The EC counts the number of cycles before the occurrence of a class III failure in the fatigue test. A wheelchair that obtained an EC score of 400,000 cycles was denoted as passing the minimum requirements of the standard.

Failure severity was classified into three levels. Any failures, such as tightening screws or bolts or inflating the tires, that could be repaired by the user or any untrained personnel were counted as class I failures. Class II failures, such as replacing tires or spokes and doing complex adjustments, need to be repaired by a wheelchair or bicycle technician . Permanent damage to the frame or any failure that would put the user in a hazardous situation was counted as a class III failure in this study. In a previous ultralight wheelchair comparison study, three bolt failures were considered class III failures . Multiple minor failures were not counted as class III failures in this study to prevent premature discontinuation that would shelter the durability of the main frame and structure. All the failures were recorded to disclose the frequency and complexity of the repairs needed for each wheelchair.

Cost-Effectiveness Knowing the cost-effectiveness of a wheelchair is meaningful. We compared the cost-effectiveness of our test wheelchairs using the value derived from normalizing the number of ECs by the retail price of the wheelchair (cycles/dollar). The higher the value, the more cost-effective the wheelchair was deemed to be .

Data Analysis We performed primary analyses for static stability, braking effectiveness, EC, and cost-effectiveness using Kruskal-Wallis tests, followed by Mann Whitney U tests as univariate analyses with the level of significance set at p 7[degrees] slope in the rearward braking effectiveness test. The frame design and the position of the dummy's lower-limbs did play an important role in affecting rearward stability as we discussed previously. The compact dimensions of the wheelchairs with rigid frames increase their maneuverability but decrease their rearward stability.

Users have to adjust their trunk posture carefully to compensate for displacement of the center of gravity when pushing one of these four wheelchair models uphill. Novice users must be educated about this behavior and trained in wheelchair skills to manage on slopes.

[FIGURE 7 OMITTED] Impact and Static Strength Tests Although the three Invacare wheelchairs that failed in the armrest static strength test were still usable, the compromised material strength of the mounting plates could have caused a catastrophic failure (Figure 5(a)). The TiLite wheelchairs had a similar mounting mechanism for the armrest as the Invacare wheelchairs, but they had a stronger structure, having double plates to support the armrest bar. All of the TiLite wheelchairs failed in the handgrip static strength tests. The hazard will occur when an attendant is pulling the wheelchair backward with an occupant in it. The attendant would tend to fall backward when the handgrips slide off the handles. Moreover, the situation may endanger the user, who could roll away uncontrolled.

Fatigue Strength Tests (Durability Testing) This group of titanium wheelchairs survived fewer ECs (their average EC was 246,506 [ or -] 154,086) than was previously reported for aluminum ultralight wheelchairs, but their life expectancy was similar to that of steel lightweight wheelchairs -. Besides, the titanium rigid-frame wheelchairs exhibited less value than the aluminum ultralight and the steel lightweight wheelchairs (Figure 8). Figure 8 shows the value of each wheelchair model for titanium ultralight rigid-frame, aluminum ultralight folding-frame, and steel lightweight wheelchairs, respectively, and the average value of each group according to the results from this and previous studies. Although the results were different among manufacturers, the wheelchairs in each group had similar performances. The survival curves (Figure 9) show each step going down, indicating class III failures of the wheelchairs from each group. With 400,000 ECs the minimum requirement of ANSI/RESNA standards, 80 percent of the aluminum ultralight wheelchairs survived but less than 40 percent of the titanium rigid-frame wheelchairs survived to comply with current standards. The aluminum ultralight wheelchairs lasted about four times longer and had a value of about eight times higher than the wheelchairs in this study. Although a smaller caster size increases the impact load on the frame compared with the larger 203 mm casters on previously tested aluminum wheelchairs, testing these titanium rigid-frame wheelchairs with 80 mm casters is reasonable based on the following.

First, 80 mm casters are the standard components of the titanium wheelchairs tested in this study. According to the clinical experience of the clinicians in the Center for Assistive Technology at the University of Pittsburgh Medical Center, most users of this group of wheelchairs were prescribed these casters. Second, 203 mm casters are not available on these wheelchairs because the footrest and likely the users' feet would interfere with the free movement of these larger sized casters. If the test results of a wheelchair with its standard components are not revealed, estimating the quality and properties of the wheelchair after adjustment or with modification may be difficult.

[FIGURE 8 OMITTED] The test results of aluminum folding wheelchairs and titanium rigid-frame wheelchairs should be compared directly, even though they have casters of different sizes. The clinical guideline recommends that manual wheelchair users use lighter wheelchairs but gives no specific recommendation on caster size . Thus, manual wheelchair users at any level of injury or wheelchair skill may choose one of the ultralight titanium rigid-frame wheelchairs with 80 mm casters tested in this study or an ultralight aluminum folding-frame wheelchair with 203 mm casters.

Therefore, all types of wheelchairs should be tested with their various components to disclose their influence on performance of the wheelchairs and all test results of different types of wheelchairs should be directly compared to provide complete information for the consumer.

[FIGURE 9 OMITTED] The wheelchairs in this study had an estimated average usable life of 1.85 to 3.08 years based on the approximation that the intensity of the ANSI/RESNA fatigue tests represents regular use for 3 to 5 years . The Invacare and TiLite wheelchairs include a lifetime warranty, and the Quickie wheelchair includes a 5-year warranty on the titanium frame. A large discrepancy seems to exist between the warranty provided by the manufacturers and the test results in this study. To provide more reliable information to the consumer, manufacturers should disclose their testing methods and setup to determine the durability of their products.

Failure Modes Invacare Top End All of the Invacare Top End wheelchairs experienced fractures of the backrest canes. On the Invacare Top End04, we found white, light blue, straw, and gray colors in the weld vicinity on the inner surface of the fracture site (Figure 10). The colors on the inner surface were within the heat-affected zone, which indicates that the titanium had high levels of oxygen contamination during the welding process . The fracture surface in the picture is quite shiny and without plastic deformation. This implies that embrittlement may have contributed to the fracture of the backrest cane.

The other two Invacare Top End wheelchairs both fractured in the same area on the backrest canes around the welding site connecting the backrest crossbar (Figure 11 (a)(i)) and the top corner of the gusset (Figure 11(a)(ii)) without the evidence of oxygen contamination. Because of the anterior and posterior movement of the dummy hitting the backrest during the DDT, the superior area of the gusset was in the bending stress concentration point of the cantilever structure .

Additionally, a hole is present at the intersection of the backrest and the backrest crossbar (Figure 11(b)-(c)) for inserting the gas flow to prevent oxygen contamination from welding. One of the backrest canes fractured at this hole (Figure 11(c)) because it further weakened the structure strength. The other three fractured backrest canes were broken at the superior edge of the weld area with the crossbar. Heat treatment from welding likely decreased the strength of the titanium canes. The Invacare Top End had the same backrest-cane wall thickness as the Quickie Ti and TiLite ZRA (1.27 mm) and was slightly thinner than the Invacare A4 (2.29 mm) (Table 6). The Invacare Top End was the only model where all chairs fractured at the backrest canes. The four factors--the cantilever structure of the backrest, one weld area for the backrest crossbar on the backrest, a second weld area for the gusset on the backrest, and the hole for inserting the gas shield--all contributed to weaken the structure. Only the depot wheelchairs in our previous comparison study had similar failure rates as the Invacare Top End .

[FIGURE 10 OMITTED] Invacare A4 The Invacare A4-06 fractured at the right caster stem and the middle of the right tube in the seat plane in the first round of the DDT (Figure 12). Although the caster stem was made of steel, the beach marks on the fracture surface indicate the occurrence of metal fatigue (Figure 12 b)-(c)) -. Because only one fractured caster stem occurred in this study, it may be considered a defective component due to a small crack developed during manufacturing. However, this finding suggests that caster-stem fracture is possible and may damage the frame and endanger the user.

There were five holes around the fracture at the middle of the right seat frame of the Invacare A4-06 (Figure 13 and Figure 14(i)). The other two Invacare A4 wheelchairs that failed in the second round of the DDT had fractures around the screw holes of the mounting plate between the backrest and seat frame and the screw holes for the seat sling (Figure 15 and Figure 14(ii)). All these holes on the frame were for the seat sling, the mounting pieces of the backrest, and the mounting bracket of the T-shaped armrest. It is very intuitive in manufacturing to drill holes for mounting components on a frame; however, the fracture lines passing through the holes implied that the structural strength was decreased by the holes. The drawing with the translucent pattern in Figure 14 shows the proximity of the holes on the frame more clearly.

The footrests of the two Invacare A4 wheelchairs repeatedly slid down during the DDT. Although both the Invacare A4 and Top End wheelchairs had footrest tubes clamped by only a set screw (Figure 16(c)), the A4 had a larger discrepancy in the diameter between the tube of the footrest and the outer piece of the main frame (Table 6). The strength of a set screw was not enough to compensate for the discrepancy in tube diameters and the vertical vibration from the dummy's legs during the DDT, so the footrest slid down. In real-world settings, a footrest keeps sliding down, bothering the user, because of the vertical vibration resulting from riding on uneven terrain or the occurrence of clonuses. Although this mounting mechanism of the footrest would not affect the integrity of the main frame, the unanticipated repositioning of the footrest can be inconvenient and potentially cause injury.

[FIGURE 11 OMITTED] Quickie Ti and TiLite ZRA The Quickie Ti and TiLite ZRA wheelchairs had the same type of failures at the first or second screw holes near the cantilever turn of the frame. These screw holes are used to mount the sling to the frame (Figure 17). Both models are cantilever frames (Figure 18(a)). The cantilever frame does not have the same lower longitudinal tubes as the box frame. The impact force (Figure 18(a)(i)) produced a bending torque (Figure 18(a)(ii)) that bent the front vertical part of the frame rearward. The bending torque compressed the lower part of the tube (Figure 18 (a)(iii)) and extended the upper part of the tube (Figure 18 (a)(iv)). The first and second screw holes were just rearward of the frame bend and acted as stress concentration points. Therefore, the fracture inevitably occurred at this location. In the box frame design (Figure 18(b)), the lower longitudinal tube helped to distribute the force transmitted to the casters (Figure 18(b)(iii)). This decreased the bending torque on the frame (Figure 18 (b)(ii)). The Invacare A4 had screw holes near the corner of the front frame as well, but the lower stresses helped protect the chair from failure at these stress concentration locations. Alternative ways are available to fix the seat sling onto the frame other than using screws. For example, the Invacare Top End Terminator everyday rigid wheelchair uses Velcro straps to attach the seat sling , which may have ameliorated the premature failures.

[FIGURE 12 OMITTED] Wheelchair Material and Design Titanium alloys have higher resistance to brittle fracture than aluminum alloys when a crack is present . Although titanium has desirable mechanical properties, titanium is 1.6 times as heavy as aluminum. Balance between total weight of the product and structural strength needs to be considered carefully. The rigid-frame design and standard use of 80 mm casters are also critical issues that affect the stability and durability of this group of wheelchairs. On the basis of our results, manufacturers and designers need to evaluate the rigid-frame titanium wheelchair designs in greater detail in order to understand the impact of material choices and mechanical design on the strength, durability, and function of the wheelchair. If the future direction will be to classify the wheelchairs with similar rigid-frame designs as those in this article into a specific group, the wheelchair standard tests may be considered to have modified testing methods and normative values for these wheelchair models.

[FIGURE 13 OMITTED] [FIGURE 14 OMITTED] [FIGURE 15 OMITTED] [FIGURE 16 OMITTED] Limitations First, the sample size is a limitation of this study. We would have to test 12 to 60 wheelchairs of each model to have statistical power of 0.8, according to the test results in this study. It is not realistic to spend the time and money to test the required number of wheelchairs.

Second, a test dummy cannot precisely simulate a real wheelchair user. A real wheelchair user could adjust his or her posture dynamically and avoid a situation that may endanger him- or herself or the wheelchair.

For example, repeated impact from the dummy's trunk during the fatigue tests may not occur in real-world situations with this group of wheelchairs, but some users hang their backpacks on the backrests, which also causes bending stress on the backrests. ANSI/RESNA standard tests were originally designed to test K0001 wheelchairs 10 years ago, thus the requirements should not be as harsh for today's technology and manufacturing quality. Moreover, the test dummy weighs less than the maximum weight capacity of the wheelchairs in this study. Although the test dummy does not mimic a real wheelchair user completely, the general physical properties of the dummy actually produce less stress than the maximum weight capacity claimed by the manufacturers. Third, we could only draw general results from standard tests because the information was not thorough enough to discriminate the specific causes or mechanisms attributed to the vital failures in the fatigue tests.

Therefore, future studies are needed to address these issues.

[FIGURE 17 OMITTED] [FIGURE 18 OMITTED] CONCLUSIONS This group of rigid-frame titanium wheelchairs is widely prescribed. Their highly adjustable rear-wheel axles, ultralight weight, and compact dimensions help decrease physical stress on the user when propelling a wheelchair and increase ease of use. This study revealed important design concerns that need to be addressed. Our results should remind manufactures and designers that each weld point, screw hole, and change in structure and frame design has its impact on the strength and durability of the wheelchair. Our results indicate that manufacturers may need to perform more careful analyses before commercializing new products.

Abbreviations: ADA = Americans with Disabilities Act, ANSI = American National Standards Institute, CDT = curbdrop test, DDT = double-drum test, EC = equivalent cycle, ISO = International Organization for Standardization, RESNA = Rehabilitation Engineering and Assistive Technology Society of North America.

ACKNOWLEDGMENTS This material was based on work supported by the Department of Veterans Affairs Rehabilitation Research and Development Service (grant B3142C) and the National Science Foundation--Integrative Graduate Education and Research Traineeship program (grant DGE 0333420).

The authors have declared that no competing interests exist.

Submitted for publication December 7, 2007. Accepted in revised form June 23, 2008.

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Hsin-yi Liu, BS; (1-2) Rory A. Cooper, PhD; (1-3) * Jonathan Pearlman, PhD; (1-2) Rosemarie Cooper, MPT, ATP; (1-2) Samuel Connor, BS (1) (1) Human Engineering Research Laboratories, Department of Veterans Affairs (VA) Rehabilitation Research and Development Service, VA Pittsburgh Healthcare System, Pittsburgh, PA; Departments of (2) Rehabilitation Sciences & Technology and (3) Bioengineering and Physical Medicine & Rehabilitation, University of Pittsburgh, Pittsburgh, PA * Address all correspondence to Rory A. Cooper, PhD; Human Engineering Research Laboratories, 151R-1HD, VA Pittsburgh Healthcare System, 7180 Highland Dr, Pittsburgh, PA 15206; 412-954-5287; fax:

412-954-5340. Email: DOI:10.1682/JRRD.2007.12.0204

Evaluation of Titanium Ultralight Manual Wheelchairs Using Ansi/resna Standards. 1

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Maikling Pagsusuri ng Kahalagahan ng Pamamahala ng Preventive Maintenance sa Medical Equipment
May-akda:MeCan Medical– Mga tagagawa ng ultrasound machines Ang modernisasyon ng ospital ay hindi mapaghihiwalay sa iba't ibang advanced na kagamitang medikal, at ang paggamit ng mga advanced na kagamitang medikal ay tumutulong sa mga doktor na mas mahusay na hatulan ang kondisyon ng pasyente. Gayunpaman, para sa mga medikal na kagamitan, mataas na katumpakan, mataas ang presyo, kumplikadong pagpapanatili, mas maikling ikot ng pag-update, ang pag-install at paggamit ng kapaligiran ng kagamitan ay nangangailangan din ng medyo mataas na mga kinakailangan. Sa ilang malalaking ospital, ang mga kagamitang medikal, bilang isang fixed asset ng ospital, ay sumasakop sa higit sa kalahati ng kabuuang halaga ng asset, at ito ay walang alinlangan na may malaking kahalagahan para sa pamamahala ng mga kagamitang medikal. Ang preventive maintenance ng mga medikal na kagamitan ay ang batayan para sa pamamahala ng mga medikal na kagamitan, pagpapahaba ng buhay ng serbisyo ng mga medikal na kagamitan, at pagpapabuti ng katumpakan ng mga medikal na kagamitan na diagnosis ng mga sakit. Samakatuwid, ito ay may malaking kabuluhan upang mapabuti ang atensyon ng pagpapanatili ng kagamitang medikal at itatag at pahusayin ang sistema ng pamamahala ng mga kagamitang medikal sa ospital. Konsepto ng preventive maintenance: Ang ibig sabihin ng preventive maintenance ay sa loob ng isang tiyak na cycle, ang device ay maaaring sistematikong suriin, makita, mapanatili, at palitan ang mga bahagi ng pagsusuot, upang ang kagamitan ay gumana nang normal. Sa pamamagitan ng preventive maintenance, ang fault rate ng kagamitan ay nababawasan, ang maintenance time ng maintenance ay nabawasan, at ang gawain ng iba't ibang gawain ay isasagawa nang maayos. Ang pangangailangan ng pagpapatupad ng anti-maintenance: Ang pagpapanatili ng mga medikal na kagamitan pagkatapos gamitin ay mahalaga. Ang pagpapatupad ng preventive maintenance ay ang regular na pagpapanatili ng mga kagamitang medikal. Sa pamamagitan ng pagpapanatili ng kagamitan upang maging pamilyar sa istruktura ng device, unawain ang kasalukuyang kagamitan. Sa panahon ng proseso ng pagpapanatili, tumpak na itinatala ng mga tauhan ng pagpapanatili ang mahahalagang kondisyon tulad ng indicator ng kagamitan at mga parameter ng trabaho, at pagkatapos ay makakagawa ng mabilis na paghuhusga sa posisyon ng fault pagkatapos i-record ang contrast pagkatapos mabigo ang kagamitang medikal. Sa pamamagitan ng preventive maintenance, ang sitwasyon ng madaling-gamitin na mga bahagi ng medikal na kagamitan, napapanahong pagbili ng mga bahagi at palitan ito, sa gayon ay binabawasan ang saklaw ng pagkabigo ng kagamitang medikal, pag-iwas sa normal na pagsusuri at paggamot ng mga pasyente dahil sa pagkabigo ng kagamitang medikal o mga aksidenteng medikal. Ang pagpapatupad ng preventive maintenance ay magpapahintulot sa mga medikal na kagamitan na tumakbo nang mahabang panahon sa isang malusog na estado, at ang buhay ng serbisyo ay pahabain. Kung gusto mong malaman ang higit pa, mangyaring bigyang-pansin ang "Prun Medical Device Network", regular kaming mag-a-update ng ilang bagong nilalaman para ma-browse at mabasa ng lahat.
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