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Joint replacement surgery in the treatment of arthritic disease is now commonplace and on the whole very successful. Research into the design and development of prostheses has made major advances since the 1940s resulting in complex devices for almost all articulating joints of the body. In this thesis, a programme of work to design and test a surface replacement prosthesis for the metacarpophalangeal joint is presented. The anatomy and kinematics of the MCP joint are discussed for both normal and abnormal joint function and, based on these considerations, the design of a new surface replacement prosthesis is described. Various materials are explored with respect to their biocompatibility, durability and ease of fabrication with special attention being paid to one material - a new cross linked ultra-high molecular weight polyethylene - which is tested for wear and assessed for durability in long-term prototype tests. A finger function simulator is detailed which was designed and developed during this research programme, and results of tests on bone replicas, Swanson Silastic implants and prototypes of the new design are presented. The simulator can be easily modified to accept any MCP joint prosthesis for bench testing. Finally the stress response of the prototype design is studied using finite element analysis and modifications to the implant design and bone preparation are suggested.

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BACKGROUND: One of the most recurrent complaints after total joint replacement is difficulty sleeping. Sleep disturbance after major surgery is common. The “stress response” to surgery, personal factors and environmental factors can affect quality and quantity of sleep in the hospital setting. Occupational therapy intervention for individuals that have problems with function as a result of sleep insufficiency is an emerging practice area. However, there are few occupational therapy practitioners who have addressed the important occupation of sleep in acute care settings. There is a need to develop science-driven research and establish evidence to support acute care occupational therapy interventions that address sleep hygiene, a set of behavioral and environmental practices designed to improve both quality and quantity of sleep. In response to this need, the author designed and carried out a non- randomized controlled study to evaluate the effectiveness of a non-pharmacological occupational therapy intervention to improve quality and quantity of clients’ sleep in a fast track joint replacement center. OBJECTIVE: In the author’s study, the aim was to compare sleep quality, sleep quantity, and activities of daily living (ADL) performance before and after fast track total joint replacement surgery for clients who received an occupational therapy intervention targeted at improving sleep hygiene, in addition to conventional acute care occupational therapy, compared to those that received only conventional acute care occupational therapy. The project focused on 1) identifying evidence-based literature to support the benefit of non-pharmacological interventions for joint replacement surgery clients, 2) designing a program that represented best practice while incorporating the holistic and occupation-based theoretical base of occupational therapy, 3) implementing the program, 4) conducting summative program evaluation, and 5) developing a dissemination plan and implementation budget. RESULTS: There were no initial significant differences between the control and experimental groups. The quality of sleep in the experimental group at discharge was significantly better than in the controls and this group reported significantly improved quality of sleep at discharge compared to 2 weeks before surgery. At discharge the experimental group reported significantly longer sleep duration compared to the control group and the increase in duration from 2 weeks before surgery to discharge was significant. CONCLUSION: The results of this study demonstrated that improvement in sleep quality and quantity can be achieved in clients undergoing fast track joint replacement surgery who receive an occupation-based intervention that incorporates implementation of sleep hygiene practices. Moreover the change appears to persist after the client returns home. More research examining the effectiveness of this intervention with other surgical populations and the persistence of learned sleep hygiene practices over time after hospital discharge are warranted. / 2018-11-07T00:00:00Z

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6 Abstract Title: Comparison of Movement Activity and Sport between Patients after Resurfacing and Total Hip Replacement Surgery Objectives: To summarize the available information about after-surgery regime and self- sufficiency after total hip replacement. To accent the differences between resurfacing and total hip replacement. To obtain the information about sport behavior and movement activity of patients after resurfacing and total hip surgery using questionnaire survey. To find out if they are able to return back to sport sctivity and how much do the total hip replacement limits them, to find out how the pain influences their movement activity. To compare the movement activity of patients after resurfacing with patients after total hip surgery. Methods: Thesis is worked out using quality assessment of information obtained by empiric way - using questionnaire survey. Results are processed using MS Excel into charts and graphs. Results: The objective of clear justification of advantages of hip resurfacing as a surgery method providing early return to movement activity has not been met. However the results cannot be simply generalized because of limited amount of respondents. Keywords: hip, total joint replacement, movement activity, sport

Wear of the polyethylene (PE) bearing surface and wear particle-induced osteolysis (bone resorption) can lead to failure of modular total knee replacements and make expensive revision surgery necessary. Gamma-in-air sterilization of the PE insert and having a modular tibial component are both risk factors for excessive backside wear that contribute to osteolysis and implant failure. The overall wear (backside and topside) of modular total knee replacements has been subjected to considerable research in order to avoid such implant failure. The investigations reported in the present thesis evaluated both the clinical and in vitro wear performance of modular total knee replacements. The clinical investigations included damage assessment of retrieved PE inserts. A semi-quantitative grading method was developed and used to assess backside surface damage on 52 PE inserts retrieved from contemporary total knee replacement surgeries. Statistical analyses, such as univariate and multiple linear regression analysis, were performed to identify factors that influence backside damage including implant design features and patient characteristics. The damage features on the retrieved tibial PE inserts were also assessed with surface characterization techniques, such as scanning electron microscopy, energy dispersive X-ray analysis, and surface profilometry. To reduce surface damage and thus wear, PE inserts should be either gas-plasma or ethylene-oxide sterilized, used with polished tibial trays and held in place with a partial-peripheral locking mechanism. Synovial fluid samples were aspirated from a total of twenty patients and some basic biochemical analyses were performed. The total protein concentration, protein constituent fractions, the level of osmolality, and trace element concentrations were measured and compared with the same characteristics of four serum lubricants that were frequently used in simulator wear testing to mimic synovial fluid. In vitro investigations were conducted to explore the effects of some major constituents of the serum lubricants on the wear rate using a knee simulator apparatus. Increased protein constituent degradation led to increased wear. Such findings suggested that a protein layer acted as a boundary lubricant to protect the PE surfaces of knee implants. The protein constituent fractions of alpha calf serum (ACS) were similar to those measured for synovial fluid. These ACS lubricants were used in further wear studies in which hyaluronic acid (HA) and phosphate buffer solution (PBS) were successively added. The PBS was used in place of the distilled water to generate a serum lubricant with a clinically relevant level of osmolality. The thermal stability of the ACS lubricants and synovial fluid were measured. The thermal stability of the ACS lubricant that contained HA and PBS was about the same as that of human synovial fluid. The simulator wear rate of PE was significantly influenced by both HA and PBS. In further investigations, sodium azide, which has been used to inhibit microbial growth in simulator wear testing, was shown to be highly ineffective. Microbial contamination was recognized and the organism responsible was identified using standard microbiological methods. The use of an antibiotic-antimycotic mixture as the microbial inhibitor in the ACS + PBS + HA lubricant created a sterile environment and thus very clinically relevant environment for wear testing. The content of this thesis represents a comprehensive data collection on retrieval analysis and lubricant-specific knee simulator wear testing of modular total knee replacements. A more clinically relevant lubricant composition for simulator wear testing was proposed (U.S. patent Serial number 60/899,894; pending since February 9th, 2007) that improved upon the current guideline from the International Standards Organization for knee simulator wear testing. The present thesis should serve as a guide for the surgeon, researcher and the implant manufacturer to evaluate retrieved implant components and to select lubricant additives for wear testing that closely mimics the in vivo wear conditions.