Our initial validation study suggests the TRAQ is a useful tool to assess transition readiness in YSHCN and to guide educational interventions by providers to support transition.
Background More aggressive management of cystic fibrosis (CF), along with the use of new therapies, has led to increasing survival. Thus, the recommended daily treatment regimens for most CF adults are complex and time consuming. Methods In the Project on Adult Care in CF (PAC-CF), an ongoing longitudinal study of CF adults, we assessed self-reported daily treatment activities and perceived treatment burden as measured by the CF Questionnaire-Revised (CFQ-R), a disease-specific quality of life measure. Results Among the 204 respondents, the median number of daily therapies reported was 7 (IQR 5-9) and the mean reported time spent on treatment activities was 108 minutes per day (SD 58 minutes). Respondents reported a median of 3 inhaled and 3 oral therapies on the day prior to the survey. Only 49% reported performing airway clearance (ACT) on that day. There were no differences in the number of medications or the time to complete therapies based on gender, age or FEV1. The mean CFQ-R treatment burden domain score was 52.3 (SD 22.1), with no significant differences in the treatment burden based on age or FEV1. In a multivariable model controlling for age, gender, and FEV1, using 2 or more nebulized medications and performing ACT for ≥30 minutes were significantly associated with increased treatment burden. Conclusion The level of daily treatment activity is high for CF adults regardless of age or disease severity. Increasing number of nebulized therapies and increased ACT time, but not gender, age, or pulmonary function, is associated with higher perceived treatment burden. Efforts to assess the effects of high treatment burden on outcomes such as quality of life are warranted.
Humans walk and run at a range of speeds. While steady locomotion at a given speed requires no net mechanical work, moving faster does demand both more positive and negative mechanical work per stride. Is this increased demand met by increasing power output at all lower limb joints or just some of them? Does running rely on different joints for power output than walking? How does this contribute to the metabolic cost of locomotion? This study examined the effects of walking and running speed on lower limb joint mechanics and metabolic cost of transport in humans. Kinematic and kinetic data for 10 participants were collected for a range of walking (0.75, 1.25, 1.75, 2.0 m s 21) and running (2.0, 2.25, 2.75, 3.25 m s 21 ) speeds. Net metabolic power was measured by indirect calorimetry. Within each gait, there was no difference in the proportion of power contributed by each joint (hip, knee, ankle) to total power across speeds. Changing from walking to running resulted in a significant ( p ¼ 0.02) shift in power production from the hip to the ankle which may explain the higher efficiency of running at speeds above 2.0 m s 21 and shed light on a potential mechanism behind the walk -run transition.
Humans walk and run over a wide range of speeds with remarkable efficiency. For steady locomotion, moving at different speeds requires the muscle-tendon units of the leg to modulate the amount of mechanical power the limb absorbs and outputs in each step. How individual muscles adapt their behavior to modulate limb power output has been examined using computer simulation and animal models, but has not been studied in vivo in humans. In this study, we used a combination of ultrasound imaging and motion analysis to examine how medial gastrocnemius (MG) muscletendon unit behavior is adjusted to meet the varying mechanical demands of different locomotor speeds during walking and running in humans. The results highlighted key differences in MG fascicle-shortening velocity with both locomotor speed and gait. Fascicle-shortening velocity at the time of peak muscle force production increased with walking speed, impairing the ability of the muscle to produce high peak forces. Switching to a running gait at 2.0 m·s −1 caused fascicle shortening at the time of peak force production to shift to much slower velocities. This velocity shift facilitated a large increase in peak muscle force and an increase in MG power output. MG fascicle velocity may be a key factor that limits the speeds humans choose to walk at, and may explain the transition from walking to running. This finding is consistent with previous modeling studies.muscle mechanics | biomechanics | preferred transition speed A nkle plantar-flexor muscles are a vital source of mechanical power for human locomotion (1, 2). During walking, plantar-flexor muscles provide body weight support, contribute to propulsion, and accelerate the limb into swing (3). In running, the ankle acts in a spring-like manner, absorbing energy in plantarflexor muscle-tendon units during early stance and providing energy to accelerate the body in late stance (1). The mechanical work required to produce whole-body movement during walking and running varies between gaits and across speeds (4, 5). Thus, the plantar-flexors may need to adjust their mechanical work output with gait and speed to meet the changing demands on their contribution to total mechanical work.A recent experimental study in humans used an inverse-dynamics approach to examine how the mechanical power outputs of muscles acting at the hip, knee, and ankle joint were modulated for walking and running at a range of speeds (6). It was found that positive power output at the ankle, in conjunction with the knee and hip, increased with walking speed. Also, Hansen et al. (7) showed that at walking speeds above those preferred, the net positive work done at the ankle increased. When switching from walking to running gait, the relative contribution of ankle positive power output to total positive power output also increased (6). It was inferred from these data that plantar-flexor muscle mechanics were adjusted to accommodate faster walking speeds and then again with the switch to running gait. If this is truly the case, then it may hav...
SUMMARYRobotic lower limb exoskeletons that can alter joint mechanical power output are novel tools for studying the relationship between the mechanics and energetics of human locomotion. We built pneumatically powered ankle exoskeletons controlled by the user's own soleus electromyography (i.e. proportional myoelectric control) to determine whether mechanical assistance at the ankle joint could reduce the metabolic cost of level, steady-speed human walking. We hypothesized that subjects would reduce their net metabolic power in proportion to the average positive mechanical power delivered by the bilateral ankle exoskeletons. Nine healthy individuals completed three 30·min sessions walking at 1.25·m·s -1 while wearing the exoskeletons. Over the three sessions, subjects' net metabolic energy expenditure during powered walking progressed from +7% to -10% of that during unpowered walking. With practice, subjects significantly reduced soleus muscle activity (by ~28% root mean square EMG, P<0.0001) and negative exoskeleton mechanical power (-0.09·W·kg -1 at the beginning of session 1 and -0.03·W·kg -1 at the end of session 3; P=0.005). Ankle joint kinematics returned to similar patterns to those observed during unpowered walking. At the end of the third session, the powered exoskeletons delivered ~63% of the average ankle joint positive mechanical power and ~22% of the total positive mechanical power generated by all of the joints summed (ankle, knee and hip) during unpowered walking. Decreases in total joint positive mechanical power due to powered ankle assistance (~22%) were not proportional to reductions in net metabolic power (~10%). The 'apparent efficiency' of the ankle joint muscle-tendon system during human walking (~0.61) was much greater than reported values of the 'muscular efficiency' of positive mechanical work for human muscle (~0.10-0.34). High ankle joint 'apparent efficiency' suggests that recoiling Achilles' tendon contributes a significant amount of ankle joint positive power during the push-off phase of walking in humans. Supplementary material available online at
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