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1.
Diabet Med ; 38(4): e14438, 2021 04.
Article in English | MEDLINE | ID: mdl-33084095

ABSTRACT

AIMS: To investigate people with Charcot midfoot deformity with regard to plantar pressure, footwear adherence and plantar foot ulcer recurrence. METHODS: Twenty people with diabetes, Charcot midfoot deformity, plantar foot ulcer history and custom-made footwear were assessed with regard to barefoot and in-shoe plantar pressures during walking, footwear adherence (% of daily steps over 7-day period) and plantar foot ulcer recurrence over 18 months. In a cohort design, they were compared to 118 people without Charcot foot (non-Charcot foot group) with custom-made footwear and similar ulcer risk factors. RESULTS: Median (interquartile range) barefoot midfoot peak pressures were significantly higher in the Charcot foot group than in the non-Charcot foot group [756 (260-1267) vs 146 (100-208) kPa; P<0.001]. In-shoe midfoot peak pressures were not significantly higher in the Charcot foot group [median (interquartile range) 152 (104-201) vs 119 (94-160) kPa] and significantly lower for all other foot regions. Participants in the Charcot foot group were significantly more adherent, especially at home, than participants in the non-Charcot foot group [median (interquartile range) 94.4 (85.4-95.0)% vs. 64.3 (25.4-85.7)%; P=0.001]. Ulcers recurred in 40% of the Charcot foot group and in 47% of the non-Charcot foot group (P=0.63); midfoot ulcers recurred significantly more in the Charcot foot group (4/8) than in the non-Charcot foot group (1/55; P=0.001). CONCLUSIONS: Effective offloading and very high footwear adherence were found in people with diabetes and Charcot midfoot deformity. While this may help protect against plantar foot ulcer recurrence, a large proportion of such people still experience ulcer recurrence. Further improvements in adherence and custom-made footwear design may be required to improve clinical outcome.


Subject(s)
Diabetic Foot , Foot Deformities, Acquired , Orthopedic Equipment , Patient Compliance/statistics & numerical data , Shoes , Aged , Cohort Studies , Diabetic Foot/epidemiology , Diabetic Foot/pathology , Diabetic Foot/physiopathology , Diabetic Foot/therapy , Female , Foot/pathology , Foot/physiopathology , Foot Deformities, Acquired/epidemiology , Foot Deformities, Acquired/pathology , Foot Deformities, Acquired/physiopathology , Foot Deformities, Acquired/therapy , Gait Disorders, Neurologic/epidemiology , Gait Disorders, Neurologic/pathology , Gait Disorders, Neurologic/physiopathology , Gait Disorders, Neurologic/therapy , Humans , Male , Middle Aged , Orthopedic Equipment/statistics & numerical data , Pressure , Recurrence , Walking/physiology
2.
J Aging Health ; 31(10_suppl): 145S-168S, 2019 12.
Article in English | MEDLINE | ID: mdl-31718412

ABSTRACT

Objective: This study examined the environmental barriers and facilitators that hinder or promote participation among adults aging with physical disabilities. Method: Data come from an ongoing study of 1,331 individuals aging with long-term physical disability (M = 65 years). Linear regression examined the association between individual and socioenvironmental factors and participation restrictions in work, leisure, and social activities. Results: Pain, fatigue, and physical functional limitations were significant barriers to participation for individuals aging with physical disability. Barriers in the built environment also reduced participation, net of health and functioning. Poor access to buildings was especially problematic for participation among individuals not using any mobility aid to get around. But for those using wheel or walking aids, environmental barriers had no adverse effect on participation. Discussion: These findings highlight the importance of disentangling the role of different environmental factors by distinguishing between assistive technology for mobility and the physical built environment, including their interactive effects.


Subject(s)
Aging , Disabled Persons/statistics & numerical data , Social Participation , Adult , Aged , Aged, 80 and over , Architectural Accessibility , Fatigue/epidemiology , Female , Humans , Male , Middle Aged , Orthopedic Equipment/statistics & numerical data , Pain/epidemiology , United States/epidemiology
3.
Arch Phys Med Rehabil ; 100(11): 2106-2112, 2019 11.
Article in English | MEDLINE | ID: mdl-31152704

ABSTRACT

OBJECTIVE: To develop a prediction model for postoperative day 3 mobility limitations in patients undergoing total knee arthroplasty (TKA). DESIGN: Prospective cohort study. SETTING: Inpatients in a tertiary care hospital. PARTICIPANTS: A sample of patients (N=2300) who underwent primary TKA in 2016-2017. INTERVENTIONS: Not applicable. MAIN OUTCOME MEASURE: Candidate predictors included demographic variables and preoperative clinical and psychosocial measures. The outcome of interest was mobility limitations on post-TKA day 3, and this was determined a priori by an ordinal mobility outcome hierarchy based on the type of the gait aids prescribed and the level of physiotherapist assistance provided. To develop the model, we fitted a multivariable proportional odds regression model with bootstrap internal validation. We used a model approximation approach to create a simplified model that approximated predictions from the full model with 95% accuracy. RESULTS: On post-TKA day 3, 11% of patients required both walkers and therapist assistance to ambulate safely. Our prediction model had a concordance index of 0.72 (95% confidence interval, 0.68-0.75) when evaluating these patients. In the simplified model, predictors of greater mobility limitations included older age, greater walking aid support required preoperatively, less preoperative knee flexion range of movement, low-volume surgeon, contralateral knee pain, higher body mass index, non-Chinese race, and greater self-reported walking limitations preoperatively. CONCLUSION: We have developed a prediction model to identify patients who are at risk for mobility limitations in the inpatient setting. When used preoperatively as part of a shared-decision making process, it can potentially influence rehabilitation strategies and facilitate discharge planning.


Subject(s)
Arthroplasty, Replacement, Knee/rehabilitation , Inpatients , Mobility Limitation , Models, Statistical , Physical Therapy Modalities , Age Factors , Aged , Aged, 80 and over , Body Mass Index , Ethnicity/statistics & numerical data , Female , Hospitals, High-Volume/statistics & numerical data , Humans , Male , Middle Aged , Orthopedic Equipment/statistics & numerical data , Pain, Postoperative , Prospective Studies , Range of Motion, Articular , Socioeconomic Factors , Tertiary Care Centers
4.
Psychol Aging ; 34(2): 208-214, 2019 Mar.
Article in English | MEDLINE | ID: mdl-30589283

ABSTRACT

Many older adults require assistive technology to maintain mobility (e.g., canes, walkers, wheelchairs, or scooters), but concerns about experiencing prejudice because of mobility devices can deter use. We explore this potential prejudice in a sample recruited through online crowdsourcing. Overall, prejudice toward older adult mobility device users was not observed. Older adult mobility device users were evaluated more positively than common prejudice target groups. However, heightened prejudice toward older adult mobility device users was observed among those higher in authoritarianism or social dominance orientation. This was explained by perceptions that older adult mobility device users are a greater threat to resources (e.g., health care spending, time, attention) among those higher in these qualities. This pattern was present at all ages assessed but was stronger for those who were younger versus older. Relationships between ideology and heightened threat from older adult mobility device users were not present for those older than 60 years of age. Our results demonstrate that concerns about this prejudice are not completely unwarranted. (PsycINFO Database Record (c) 2019 APA, all rights reserved).


Subject(s)
Orthopedic Equipment/statistics & numerical data , Prejudice , Self-Help Devices/psychology , Self-Help Devices/statistics & numerical data , Social Perception , Aged , Aging , Canes/statistics & numerical data , Female , Humans , Male , Middle Aged , Walkers/statistics & numerical data , Wheelchairs/statistics & numerical data
5.
Salud Publica Mex ; 60(4): 462-471, 2018.
Article in English | MEDLINE | ID: mdl-30137948

ABSTRACT

OBJECTIVE: To analyze the role of stakeholders to three alternative strategies to improve processes and practices regarding the regulation, assessment, and management of orthopaedic medical devices in Mexico. MATERIALS AND METHODS: The study was based on document analysis and 17 structured interviews with multiple key actors within the Mexican health system to inform a stakeholder analysis aiming at assessing the political feasibility of these strategies. RESULTS: Central level government agencies, those with a relation to quality of care, were identified as most relevant stakeholders to influence the adaption and application of the strategies. Major barriers identified are financial and human resources, and organisational culture towards reform. CONCLUSIONS: Discussed strategies are political feasible. However, solving identified barriers is crucial to achieve changes directed to improve outputs and outcomes of medical device life cycle and positively influence the quality of health care and the health system's performance.


Subject(s)
Orthopedic Equipment , Feasibility Studies , Female , Government Agencies , Humans , Male , Mexico , Orthopedic Equipment/economics , Orthopedic Equipment/statistics & numerical data , Orthopedic Equipment/supply & distribution , Public Policy , Stakeholder Participation , Surveys and Questionnaires
6.
Salud pública Méx ; 60(4): 462-471, Jul.-Aug. 2018. tab
Article in English | LILACS | ID: biblio-979155

ABSTRACT

Abstract Objective To analyze the role of stakeholders to three alternative strategies to improve processes and practices regarding the regulation, assessment, and management of orthopaedic medical devices in Mexico. Materials and methods The study was based on document analysis and 17 structured interviews with multiple key actors within the Mexican health system to inform a stakeholder analysis aiming at assessing the political feasibility of these strategies. Results Central level government agencies, those with a relation to quality of care, were identified as most relevant stakeholders to influence the adaption and application of the strategies. Major barriers identified are financial and human resources, and organisational culture towards reform. Conclusion Discussed strategies are political feasible. However, solving identified barriers is crucial to achieve changes directed to improve outputs and outcomes of medical device life cycle and positively influence the quality of health care and the health system's performance.


Resumen Objetivo Analizar el papel de actores clave ante tres estrategias para mejorar los procesos y prácticas relacionados con la regulación, evaluación y gestión de dispositivos médicos ortopédicos en México. Material y métodos Análisis de grupos de interés (stakeholder analysis) basado en un análisis documental y 17 entrevistas estructuradas con actores clave, dirigido a evaluar la viabilidad política de las estrategias. Resultados El papel de las agencias federales de gobierno, principalmente las relacionadas con calidad de atención, fue identificado como central y con mayor poder para influenciar la adaptación y aplicación de las estrategias. Como barreras se identificaron los recursos financieros y humanos, y reorientar la cultura organizacional hacia la reforma. Conclusión Las estrategias discutidas son políticamente viables. Resolver las barreras es importante para lograr cambios que optimicen el ciclo de vida de los dispositivos médicos e influyan positivamente en la calidad de atención y el desempeño del sistema de salud.


Subject(s)
Humans , Male , Female , Orthopedic Equipment/economics , Orthopedic Equipment/supply & distribution , Orthopedic Equipment/statistics & numerical data , Public Policy , Feasibility Studies , Surveys and Questionnaires , Stakeholder Participation , Government Agencies , Mexico
7.
Can J Occup Ther ; 85(2): 106-116, 2018 Apr.
Article in English | MEDLINE | ID: mdl-29661073

ABSTRACT

BACKGROUND: Opportunities to travel from one place to another in the community, or community mobility, are especially important for mobility device users' ability to participate fully in society. However, contextual challenges to such mobility exist. PURPOSE: This study summarizes the literature on existing community mobility barriers and facilitators of mobility device users created by services, systems, and policies as defined by the International Classification of Functioning, Disability, and Health (ICF). METHOD: Arksey and O'Malley's approach for scoping studies was used for the review. The extraction chart was organized following the ICF, and frequency counts were used to report the data. FINDINGS: The findings suggest that certain factors, such as transportation, open-space planning, and architecture and construction, influence community mobility opportunities. However, little attention has been paid to services, systems, and policies in the research literature, limiting the knowledge on the subject. IMPLICATIONS: Further research is needed to examine the relationship between specific services, systems, and policies and mobility device users' mobility within their communities.


Subject(s)
Disabled Persons/rehabilitation , Occupational Therapy/organization & administration , Orthopedic Equipment/statistics & numerical data , Policy , Self-Help Devices/statistics & numerical data , Architectural Accessibility , Environment Design , Humans , Occupational Therapy/standards , Transportation
8.
Int Orthop ; 42(8): 1845-1851, 2018 08.
Article in English | MEDLINE | ID: mdl-29396803

ABSTRACT

BACKGROUND AND PURPOSE: Anterior knee laxity can be evaluated using different devices, the most commonly used being the Telos®, KT1000®, Rolimeter®, and GNRB®. However, the laxity values obtained with these devices have never been compared to one another. As such, the outcomes of studies using these different knee laxity measurement devices may not be comparable. The primary purpose of this study was to determine the side-to-side laxity difference in patients with one ACL-injured knee, using each of these devices, and to compare the values obtained from each. We hypothesized that the measurements of laxity would vary depending on the device used. METHODS: This was a prospective study. All patients with an ACL injury, in which surgical reconstruction was planned, underwent pre-operative knee laxity measurements using four different devices. The concordance correlation coefficient (CCC) of the results was compared between the four devices. RESULTS: The study enrolled 52 patients. With regard to the values of the side-to-side differences, the KT1000® and the GNRB® obtained the most similar values (CCC = 0.51, 95% CI 0.37-0.63). The two devices with the lowest correlation were the Telos® and the Rolimeter® (CCC = 0.04, 95% CI - 0.14-0.23). The comparability was considered average for the KT1000® and GNRB® and poor for the other devices. CONCLUSIONS: The knee laxity devices used in regular practice are not comparable to one another. As a result, caution must be taken when comparing results from studies using these different devices.


Subject(s)
Anterior Cruciate Ligament Injuries/physiopathology , Diagnostic Techniques and Procedures/instrumentation , Joint Instability/diagnosis , Knee Joint/physiopathology , Orthopedic Equipment/statistics & numerical data , Adult , Female , Humans , Male , Preoperative Care/methods , Prospective Studies , Range of Motion, Articular/physiology , Young Adult
9.
HERD ; 11(4): 65-81, 2018 Oct.
Article in English | MEDLINE | ID: mdl-29417846

ABSTRACT

AIM:: The main purpose of this research was to identify significant relationships between environmental hazards and older adults' falling. BACKGROUND:: Falls can present a major health risk to older persons. Identifying potential environmental hazards that increase fall risks can be effective for developing fall prevention strategies that can create safer residential environments for older adults. METHODS:: The research included a retrospective analysis of 449 fall incident reports in two case-control buildings. In the homes of 88 older adults residing in independent living, an observational study was conducted to identify environmental hazards using two assessment tools including Westmead Home Safety Assessment (WeHSA) and resident interviews. RESULTS:: A fall history analysis indicated that falls occurred in the bathroom were significantly associated with hospitalization. The observational study revealed that the bathroom was the most common place for environmental hazards. The research showed, with increasing age and use of mobility assistive aids, there was a corresponding increase in the total number of environmental hazards. Home hazards were significantly and independently associated with the incidence rate of falls. In other words, the high fall rate building included more environmental hazards compared to the low fall rate building while controlling for residents' age and mobility. CONCLUSION:: The current study provides empirical evidence of the link between environmental hazards and older adults' falling, which is useful for developing effective fall intervention design strategies.


Subject(s)
Accidental Falls/statistics & numerical data , Independent Living/standards , Interior Design and Furnishings , Age Factors , Aged , Aged, 80 and over , Case-Control Studies , Female , Hospitalization/statistics & numerical data , Humans , Male , Orthopedic Equipment/statistics & numerical data , Retrospective Studies , Risk Factors , Toilet Facilities
10.
Int Orthop ; 42(6): 1291-1296, 2018 06.
Article in English | MEDLINE | ID: mdl-29379983

ABSTRACT

PURPOSE: Cortical suspensory devices are routinely used for femoral side fixation of soft tissue graft in anterior cruciate ligament (ACL) reconstruction. The purpose of this study was to evaluate the biomechanical properties of a new adjustable loop device (GraftMax®) compared with established devices (EndoButton® and TightRope®) in ACL reconstruction and to investigate whether knotting the free end of TightRope could improve biomechanical properties. METHODS: The three cortical suspensory devices (GraftMax® Button; Conmed, EndoButton® CL; Smith & Nephew, and TightRope® RT; Arthrex) were tested under cyclic load (50-250 N for 1000 cycles) and pull-to-failure conditions at 50 mm/h in a device-only setup using a tensile testing machine. The TightRope was additionally tested with its free suture ends knotted. The statistical analyses were done with one-way analysis of variance (ANOVA) and post hoc Tukey HSD tests. RESULTS: There are significant differences in the load-to-failure among the devices. The EndoButton showed the highest mean failure load at 1204.7 N compared to other devices (GraftMax (914.2 N), knotted TightRope (868.1 N) and TightRope (800.1 N) (p < 0.001). The mean total displacement after 1000 cycles was 0.76 mm, 2.11 mm, 1.56 mm and 1.38 mm for the EndoButton, GraftMax, TightRope, and knotted TightRope, respectively. The EndoButton showed significantly better properties than both the GraftMax (p = 0.000) and the TightRope (p = 0.020) but not the knotted TightRope (p = n.s.) in total displacement. However, there was no significant difference between the TightRope and GraftMax (p = n.s.). CONCLUSION: The fixed loop (EndoButton) showed significantly better mechanical properties in failure load and displacement than TightRope or GraftMax in this biomechanical study. However, the mechanical properties of the GraftMax is comparable to the TightRope. Moreover, the knotting of TightRope improved mechanical properties in total displacement more than TightRope, but not in failure load. CLINICAL RELEVANCE: The biomechanical properties of the GraftMax are comparable to the TightRope. The TightRope, when knotted, shows an improvement both in load to failure and cyclic displacement, though the differences are not significant.


Subject(s)
Anterior Cruciate Ligament Reconstruction/instrumentation , Anterior Cruciate Ligament/surgery , Equipment Failure/statistics & numerical data , Orthopedic Equipment/statistics & numerical data , Biomechanical Phenomena/physiology , Orthopedic Equipment/adverse effects
11.
Occup Ther Int ; 2017: 5612843, 2017.
Article in English | MEDLINE | ID: mdl-29097973

ABSTRACT

Assistive technology was once a specialised field of practice, involving products designed for populations with specific impairments or functional goals. In Australia, occupational therapists have, at times, functioned as gatekeepers to public funding, prescribing products from a predefined list. An expanding range of accessible mainstream products available via international and online markets has changed the meaning and application of assistive technology for many people with disability. In the policy context of consumer choice and cost-effectiveness, have occupational therapists been left behind? This paper describes the change in context for access to assistive technology resulting in expanded possibilities for participation and inclusion. A case study of environmental control systems is used to explore the overlap of mainstream and assistive products and the funding and services to support their uptake. The analysis describes a future policy and practice context in which assistive technology includes a spectrum of products decoupled from access to independent advice and support services. A broader scope of occupational therapy practice has potential to enhance the occupational rights of people with disability and the efficiency and effectiveness of assistive technology provision.


Subject(s)
Disabled Persons/rehabilitation , Occupational Therapists/standards , Occupational Therapy/methods , Orthopedic Equipment/statistics & numerical data , Self-Help Devices/statistics & numerical data , Australia , Humans
12.
Am J Phys Med Rehabil ; 96(12): 894-903, 2017 Dec.
Article in English | MEDLINE | ID: mdl-29176406

ABSTRACT

In this systematic literature review, we examined whether and how walking aids (i.e., canes, crutches, walkers, and rollators) enable activity and participation among adults with physical disabilities. Medline, Embase, all EBM reviews, PsychInfo, CINAHL, and Web of Science databases were used to identify studies published since 2008. Quantitative and qualitative designs were included. Data regarding participants, assistive device use, outcome measures, and domains of participation were extracted. Two reviewers independently rated the level of evidence and methodological quality of the studies. Outcomes were categorized per types of walking aids and activity and participation domains. Thirteen studies were included. Two studies involved canes, four pertained to rollators, and seven dealt with multiple types of walking aids. Mobility was the most frequently examined domain of activity and participation. Both negative and positive results were found. Negative outcomes were linked to the physical characteristics of the device, the use, environment, and personal reluctance. When incorporated in daily life, walking aids were found to enable several domains of activity and participation. Whether walking aids facilitate activity and participation may depend on the user's ability to overcome obstacles and integrate them in daily life. More high-quality research is needed to draw conclusions about their effectiveness.


Subject(s)
Disabled Persons/rehabilitation , Orthopedic Equipment/statistics & numerical data , Quality of Life , Self-Help Devices/statistics & numerical data , Walking/physiology , Canes/statistics & numerical data , Crutches/statistics & numerical data , Disability Evaluation , Evaluation Studies as Topic , Female , Humans , Male , Treatment Outcome , Walkers/statistics & numerical data , Walking/psychology
13.
Arq. bras. med. vet. zootec. (Online) ; 69(4): 933-940, jul.-ago. 2017. ilus, tab
Article in Portuguese | LILACS, VETINDEX | ID: biblio-876687

ABSTRACT

Fraturas costumam ocorrer com encavalgamento das extremidades ósseas, dificultando, assim, sua redução. Esta pesquisa teve como objetivo desenvolver um equipamento de tração esquelética a ser utilizado em caninos acometidos de fraturas de ossos longos. Foram utilizados 21 cães de raças variadas, pesando entre dois e 27kg, com idade entre dois meses e 11 anos, com fraturas diafisárias ou metafisárias ocorridas entre três e 24 dias. Enquanto a fixação do corpo do paciente à mesa foi efetuada com cintas de náilon, a força de tração aplicada ao longo do eixo ósseo do membro fraturado foi realizada mediante cintas de náilon ou pinos transfixados e estribos (sendo os pinos implantados na epífise distal do osso fraturado), com a força de tração medida por um dinamômetro, não sendo aplicada carga maior que 25kg. Em todos os casos, a força de tração iniciava com o valor de cinco quilogramas, exceto em animais com peso inferior a esta, a qual começava com carga equivalente a esse peso; e em todos, se necessário, era aumentada a cada cinco minutos para se manter tração igual ao peso ou aos valores que oscilavam do seu peso até cinco quilogramas, dependendo do tamanho do animal, até se atingir a tração necessária para se proceder à redução. Para essa progressão de distensão, o equipamento possuía haste rosqueada de 25mm de diâmetro, uma porca com sistema timão e cilindro deslizante por fora da haste, este conectado ao animal por uma corrente, e o dinamômetro. Todos os animais tiveram as fraturas reduzidas sem haver perda óssea, o que evidencia que o aparelho se mostrou eficiente tanto na redução como na manutenção da redução da fratura, e eles não apresentaram, no pós-operatório, sinais de prejuízos neurológicos, vasculares, cutâneos e articulares. O distensor ósseo aqui desenvolvido tem como características: ser de simples confecção, ter baixo custo, não gerar danos ao paciente e facilitar a redução dos fragmentos tanto em fraturas recentes quanto em antigas.(AU)


Fractures usually occur with overriding of bone fragments, thus hindering fracture reduction. The aim of this research was to develop and test a skeletal traction device for use in dogs with long bone fractures. Twenty-one dogs were included, regardless of breed or gender, weighing between two and 27kg, and between two months and 11 years of age, with metaphyseal or diaphyseal fractures that had occurred between three and 24 days prior to intervention. While fixation of the patient's body to the table was performed using nylon straps, the traction force applied along the bone axis of the fractured limb was performed using nylon straps or transfixed pins and stirrups (with the pins implanted in the distal epiphysis of the fractured bone). Tensile strength was measured by a dynamometer, and the maximum load applied was no greater than 25kg. In all cases, the distraction force began at five kilograms except in dogs below this weight, where the starting load was equivalent to the weight of the animal. If necessary, in all dogs, force was increased every five minutes to maintain equal traction to the dog's weight or values which ranged from the dog's weight to five kilograms depending on the size of the animal, until the necessary traction for reduction was obtained. For this progression of distension, the equipment had a 25-milimeter-diameter threaded rod, a nut with a rudder system and sliding cylinder outside the rod, which connected to the dog via a chain and the dynamometer. Fracture reduction was achieved in all dogs without bone loss, and the device was shown to be efficient in both allowing and maintaining fracture reduction, with no neurologic, vascular, cutaneous, or articular damage. The developed bone distractor has the following characteristics: simple to construct, low cost, does not harm the patient, and facilitates reduction of the fragments in recent and old fractures.(AU)


Subject(s)
Animals , Dogs , Fractures, Bone/veterinary , Orthopedic Equipment/statistics & numerical data , Orthopedic Equipment/veterinary , Traction/statistics & numerical data
14.
J Bone Joint Surg Am ; 99(7): e33, 2017 Apr 05.
Article in English | MEDLINE | ID: mdl-28375897

ABSTRACT

BACKGROUND: Orthopaedic procedures are expensive, and devices account for a large proportion of the overall costs. Hospitals have employed a variety of strategies to decrease implant costs, but many center on restricting surgeon choice. At our institution, we developed an implant selection tool that guides surgeons toward more cost-effective implants, while minimally restricting choice. The purpose of this study was to assess the effect of this tool on preferred implant usage rates, vendor attitudes toward pricing structure, and hospital implant expenditures. METHODS: For 6 commonly used orthopaedic trauma devices, similar constructs were created for the 4 vendors used at our hospital, and the costs were determined. On the basis of these costs, the available options for each device type were categorized as "green" (preferred vendor), "yellow" (midrange), or "red" (used for patient-specific requirements). The "Red-Yellow-Green" chart was posted on the wall of each orthopaedic trauma operating room. To assess the effect of the tool, we compared implant usage patterns before and after implementation of the implant selection tool. We also assessed changes in vendor contract prices, as well as overall savings to our institution. RESULTS: Implant usage changed significantly from 30% "red," 56% "yellow," and 14% "green" prior to the intervention, to 9% "red," 21% "yellow," and 70% "green" after the intervention (p < 0.0001). As a result of price renegotiation with vendors following implementation, we observed average price decreases that ranged from 1.1% to 22.4%. Average expenditures on these 6 implants decreased 20% during the study period, which represented a savings of $216,495 per year. CONCLUSIONS: At our institution, we designed and implemented "Red-Yellow-Green," a simple tool that guides surgeons toward the selection of lower-cost implants without violating vendor confidentiality clauses, limiting the implants from which surgeons can choose, or requiring surgeons to discern the prices of complex constructs. Following implementation, hospital implant expenditures decreased as a result of a combination of increased preferred vendor usage by surgeons, as well as increased competition among vendors, which resulted in lower overall prices.


Subject(s)
Clinical Decision-Making/methods , Orthopedic Equipment/statistics & numerical data , Orthopedic Surgeons/psychology , Prostheses and Implants/statistics & numerical data , Baltimore , Color , Cost Savings , Decision Support Techniques , Health Expenditures , Humans , Middle Aged , Orthopedic Equipment/economics , Orthopedic Surgeons/economics , Prostheses and Implants/economics
16.
Spine J ; 17(1): 150-157, 2017 01.
Article in English | MEDLINE | ID: mdl-27737804

ABSTRACT

BACKGROUND CONTEXT: Recently, there has been increased public awareness of regulatory actions by the United States Food and Drug Administration (FDA) on spinal devices. There has also been increased scrutiny of the pivotal clinical trials of these devices. PURPOSE: To investigate the premarket approval (PMA) of class III spinal devices in the United States since the turn of the century. To explore clinically relevant issues that affect the interpretation of investigational device exemption trials. STUDY DESIGN: Literature review. METHODS: From 2000 to 2015, data on PMA applications for spinal devices were obtained from two sources. First, meetings of FDA's Orthopaedic and Rehabilitation Devices Panel were identified from the Federal Register. Second, the FDA database of approved PMA applications was queried. For each device, two authors reviewed all archival data. There was no external source of funding. RESULTS: Twenty-one devices met the study criteria. There were 76.2% that received approval and 47.6% that went to panel. Arthroplasty devices were most common (52.4%), least likely to go to panel (3 of 11), and most likely to be approved after panel (3 of 3). Biologic devices were most likely to go to panel (3 of 3) and least likely to be approved after panel (1 of 3). Before and after 2009, there was no decrease in the number of spinal devices approved. All 21 devices were studied in a pivotal clinical trial. All trials except one were randomized controlled trials, and all trials except one were two-arm noninferiority designs. CONCLUSIONS: There has been no decrease in the number of new FDA-approved class III spinal devices since the turn of the century. The majority of devices have been for cervical arthroplasty. By contrast, biologic devices were most likely to go to panel and least likely to be approved after panel. The pivotal trials for nearly all devices were randomized, two-arm, noninferiority trials.


Subject(s)
Clinical Trials as Topic/standards , Device Approval/standards , Orthopedic Equipment/standards , Arthroplasty/instrumentation , Humans , Orthopedic Equipment/economics , Orthopedic Equipment/statistics & numerical data , United States
17.
J Orthop Trauma ; 30 Suppl 5: S27-S31, 2016 Dec.
Article in English | MEDLINE | ID: mdl-27870671

ABSTRACT

OBJECTIVES: To determine the role of generic orthopaedic trauma implants in the current orthopaedic trauma market, as perceived by OTA members, and investigate potential hurdles to the use of generic implants and other cost-containment measures. DESIGN: Survey study. SETTING: Not applicable. PARTICIPANTS: All active OTA members with valid e-mail addresses were invited to participate. INTERVENTION: Participants completed a brief online survey with questions regarding participation in cost-containment and incentive programs, industry relationships, generic implant use, and the role of surgeons in cost containment. MAIN OUTCOME MEASURES: Survey data. RESULTS: Participation in cost-containment programs (comanagement agreements, bundled payment for care improvement, and gainsharing) was found to be very low among participants (17%, 36.5%, 17%, respectively). Industry sales representatives were present in a majority of participants' cases (76.9%) the majority of time, but relatively a few surgeons (21.2%) felt their presence was necessary. Most surgeons were aware of the availability of generic implants (72.6%), but a few had adopted the use of such implants (25.5%), despite 50/52 (96.2%) prescribing generic drugs and 45/52 (86.5%) using generic products in their own households. CONCLUSIONS: Most participants agreed that generic orthopaedic implants have a role in cost containment, but a few have adopted these implants. The presence of sales representatives does not seem to be necessary for most surgeons, and minimizing or eliminating their presence may result in substantial savings for health care institutions. Increased education and the use of financial incentive programs may encourage improved surgeon participation in cost containment and adoption of generic implants and may help reduce health care spending. LEVEL OF EVIDENCE: Level 4. See Instructions for Authors for a complete description of levels of evidence.


Subject(s)
Attitude of Health Personnel , Orthopedic Equipment/economics , Orthopedic Equipment/statistics & numerical data , Orthopedic Surgeons/economics , Orthopedic Surgeons/statistics & numerical data , Prostheses and Implants/economics , Prostheses and Implants/statistics & numerical data , Health Knowledge, Attitudes, Practice , Orthopedics/economics , Orthopedics/statistics & numerical data , Surveys and Questionnaires , United States
18.
J Orthop Trauma ; 30 Suppl 5: S37-S39, 2016 Dec.
Article in English | MEDLINE | ID: mdl-27870673

ABSTRACT

Implant costs comprise the largest proportion of operating room supply costs for orthopedic trauma care. Over the years, hospitals have devised several methods of controlling these costs with the help of physicians. With increasing economic pressure, these negotiations have a tremendous ability to decrease the cost of trauma care. In the past, physicians have taken no responsibility for implant pricing which has made cost control difficult. The reasons have been multifactorial. However, industry surgeon consulting fees, research support, and surgeon comfort with certain implant systems have played a large role in slowing adoption of cost-control measures. With the advent of physician gainsharing and comanagement agreements, physicians now have impetus to change. At our facility, we have used 3 methods for cost containment since 2009: dual vendor, matrix pricing, and sole-source contracting. Each has been increasingly successful, resulting in massive savings for the institution. This article describes the process and benefits of each model.


Subject(s)
Commerce/economics , Contract Services/economics , Cost Control/economics , Economic Competition/economics , Health Care Costs/statistics & numerical data , Orthopedic Equipment/economics , Prostheses and Implants/economics , Commerce/statistics & numerical data , Contract Services/statistics & numerical data , Cost Control/statistics & numerical data , Economic Competition/statistics & numerical data , Models, Economic , Nevada/epidemiology , Orthopedic Equipment/statistics & numerical data , Prostheses and Implants/statistics & numerical data , Utilization Review
19.
N Z Med J ; 129(1437): 15-26, 2016 Jul 01.
Article in English | MEDLINE | ID: mdl-27362595

ABSTRACT

AIMS: The aims of this audit were to collect the Minimum Data Set outlined by the Australia New Zealand Hip Fracture Registry (ANZHFR), assess patient characteristics, analyse process of care, and evaluate how this compares to NICE guidelines for hip fracture care, as well as to Auckland Hospital data from 2007. METHOD: Retrospective case record audit of patients with fractured neck of femur aged 65 years and over admitted under Orthopaedics over a 4-month period in 2013. RESULTS: Ninety-one patients were audited; mean age was 83 years, 68% were female. Both inpatient and 30-day mortality was 5%. 120-day mortality was 15%. Seventy-six percent of patients were admitted from ED within the national health target prescribed period of 6 hours. Only one patient was treated non-surgically. Eighty-six percent had surgery within 48 hours of admission. Eighty-two percent of patients had rehabilitation and treatment by Older People's Health. Of those living at home pre-fracture, 76% returned home on discharge. Thirty-seven percent of patients were able to walk unaided prior to hip fracture, but only 1% on discharge. Average overall length of stay was 22 days. Bisphosphonates were prescribed for 56% of patients. CONCLUSIONS: Compared to 2007, Auckland City Hospital has demonstrated a significant improvement in the rate of provision of timely surgery for hip fracture patients. Most patients are receiving the guideline recommended fracture-specific surgical interventions. The assessment and treatment of osteoporosis needs further attention.


Subject(s)
Clinical Audit , Femoral Neck Fractures/epidemiology , Femoral Neck Fractures/surgery , Aged , Aged, 80 and over , Arthroplasty, Replacement, Hip/statistics & numerical data , Bone Density Conservation Agents/administration & dosage , Cognitive Dysfunction/epidemiology , Comorbidity , Dementia/epidemiology , Diphosphonates/administration & dosage , Emergency Service, Hospital/statistics & numerical data , Female , Femoral Neck Fractures/rehabilitation , Fracture Fixation, Internal/statistics & numerical data , Geriatric Assessment/statistics & numerical data , Hemiarthroplasty/statistics & numerical data , Hospital Mortality , Hospitals, Urban , Humans , Length of Stay/statistics & numerical data , Male , New Zealand/epidemiology , Orthopedic Equipment/statistics & numerical data , Patient Discharge/statistics & numerical data , Platelet Aggregation Inhibitors/therapeutic use , Postoperative Complications/epidemiology , Rehabilitation/statistics & numerical data , Retrospective Studies , Time-to-Treatment/statistics & numerical data , Venous Thrombosis/prevention & control
20.
Osteoarthritis Cartilage ; 23(12): 2141-2149, 2015 Dec.
Article in English | MEDLINE | ID: mdl-26187575

ABSTRACT

OBJECTIVE: To characterize groups of subjects according to their trajectory of knee pain and function over 1 to 5 years post total knee arthroplasty (TKA). METHODS: Patients from one centre who underwent primary TKA (N = 689) between 2006 and 2008. The Knee Society Score (KSS) was collected pre-operatively and annually post-operatively. Latent Class Growth Analysis (LCGA) was used to classify groups of subjects according to their trajectory of knee pain and function over 1-5 years post-surgery. RESULTS: LCGA identified a class of patients with persistent moderate knee pain (22.0%). Predictors (OR, 95% CI) of moderate pain trajectory class membership were pre-surgery SF12 mental component summary (MCS) per 10 points (0.65, 0.54-0.79) and physical component summary (PCS) per 10 points (0.50, 0.33-0.76), Charlson Comorbidity Index (CCI) one (1.70, 1.07-2.69) and ≥two (2.82, 1.59-4.81) and the absence of computer-navigation (2.26, 1.09-4.68). LCGA also identified a class of patients with poor function (23.0%). Predictors of low function trajectory class membership were, female sex (3.31, 1.95-5.63), advancing age per 10 years (2.27, 1.69-3.02), pre-surgery PCS per 10 points (0.50, 0.33-0.74), obesity (1.69, 1.05-2.72), morbid obesity (3.12, 1.55-6.27) and CCI ≥two (2.50, 1.41-4.42). CONCLUSIONS: Modifiable predictors of poor response to TKA included baseline co-morbidity, physical and mental well-being and obesity. This provides useful information for clinicians in terms of informing patients of the expected course of longer term outcomes of TKA and for developing prediction algorithms that identify patients in whom there is a high likelihood of poor surgical response.


Subject(s)
Arthroplasty, Replacement, Knee , Osteoarthritis, Knee/surgery , Pain/physiopathology , Registries , Statistics as Topic , Aged , Comorbidity , Female , Humans , Logistic Models , Male , Mental Health , Middle Aged , Mobility Limitation , Multivariate Analysis , Obesity/epidemiology , Orthopedic Equipment/statistics & numerical data , Osteoarthritis, Knee/complications , Osteoarthritis, Knee/epidemiology , Osteoarthritis, Knee/physiopathology , Pain/etiology , Risk Factors , Treatment Outcome
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