REHABILITATION AFTER STROKE

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CHAPTER 48 REHABILITATION AFTER STROKE

Stroke, or vascular brain injury, has an incidence of between about 1.1 and 2.6 per 1000 adults1 and a prevalence of 5 to 8 per 1000.2 It is a leading cause of chronic disability worldwide; in the United Kingdom, it is the commonest single cause of severe disability in people living at home.3,4 About 75% of affected patients are older than 65 years, and 10% are younger than 55. Each year in England and Wales, stroke occurs in about 10,000 people younger than 55 and 1000 people younger than 30. Six to 12 months after stroke, only 60% of patients with hemiplegic stroke have achieved independence in personal care, and those with sensory or visual field loss are more disabled; 30% to 40% of survivors are depressed, 10% to 15% severely so; 50% need help with either housework, meal preparation, or shopping; and a similar percentage lack a meaningful social, recreational, or occupational activity during the day.58 In addition to the personal consequences, the economic consequences of stroke are also enormous; direct health care costs account for approximately 4% of total health care costs, or about £3 billion in the United Kingdom (about $5.3 billion in U.S. dollars) per annum at 2005 prices9; these costs will increase as the population ages.

Neuroprotective interventions to reverse the immediate consequences of stroke are not widely applicable.10 In these circumstances, when reversal of pathology is incomplete, the majority of stroke survivors need the multidimensional process termed rehabilitation to enhance their functional activity and societal participation and to reduce the effect of limitations in these areas, so that life quality is improved and life is “worth living.”11 Rehabilitation goals are achieved through the prevention of secondary complications; through facilitation of neural protection, restoration, and substitution; and through functional compensation, which involves both behavioral adaptation and substitution, as well as modification of personal, environmental, and social contextual factors (Table 48-1). This process must also be accompanied by often difficult and less frequently admitted adjustment to loss and change, a need that is easily forgotten in the gym or during a functional imaging study. This chapter explores the delivery and effectiveness of these interventions during rehabilitation after stroke.

TABLE 48-1 Mechanisms of Recovery after Stroke

The high incidence and prevalence of stroke have provided an opportunity to test the effectiveness of many components of the rehabilitation process. Trials have shown convincingly that organized care produces better outcomes than disorganized care; this result has far-reaching implications for health care systems in general, let alone those focusing on stroke. Many of the areas addressed in this chapter are included in evidence- and expert opinion–based guidelines produced in the United Kingdom by the Royal College of Physicians12 and the Scottish Intercollegiate Guidelines Network,13 in Australia by the National Stroke Foundation,14 and in the United States by the Department of Veterans Affairs and the Department of Defense.15

COMPLEX ORGANIZATIONAL INTERVENTIONS

Rehabilitation after single-incident brain injury, including stroke, should be delivered through polymodal inpatient and community-based service delivery systems that differ by structure and process. A classification of these different service options, as a “rehabilitation typology,” remains to be agreed upon, at least cross-culturally, and would facilitate comparisons of different studies.16 The use of each component is determined by a variety of clinical and social factors, including length of time since injury, level of dependency, characteristics of the residual impairment, age of the patient, and resources available.17 Recommendations that different types of care after stroke are incorporated into systems of clinical care (e.g., Schwamm et al18) also emphasize the use of acute and rehabilitation interventions in parallel rather than in series (Fig. 48-1), so that strategies optimizing neural protection acutely are combined with key factors identified in postacute care. The benefits of organized complex polymodal interventions so far reported are likely to reflect mainly the effects of preventing the complications described later in this chapter and shown in Table 48-2, functional interventions that focus on teaching new skills, and the use of aids and appliances and environmental modifications to help patients adapt to their impairments, rather than the effects of neural reorganization.

TABLE 48-2 Complications after Stroke during Inpatient Rehabilitation and Their Management

Cause and Effect Stroke Unit Frequency % (95% Confidence Interval) Management
Comorbid Conditions
Hypertension/hypotension 15/8199 Antihypertensive/treat cause
Cardiac events 13199 Specific medical treatments
Fever 20199 Antipyretics
GI bleed 3196/4199 ? Prophylaxis; avoid NSAIDs
Drug side effects 9198 Drug withdrawal
Musculoskeletal pain 14198/38197 Physical therapies
Physical Dependency
Pressure sores 4198 Pressure care, 24-hr handling and positioning
Sores and skin breaks 21 (16-25)195/18196  
Contractures    
PEs and DVTs 3 (0-3)195/5198 Thromboprophylaxis
Falls 25 (21-30)195/20256/11198 Risk assessment
Shoulder pain 9 (6-12)195/24256 Handling and positioning
Neurological Damage
Malnutrition and dehydration 5198 and 10198/10199 NG/PEG feeding and dietetics
Chest infections 22 (18-27)195/4199 Dysphagia management
Urinary tract infections 23 (18-28)195/15256/31198 Toileting program
Confusion and agitation 36 (30-41)195/4199 Environmental management ± drugs
Epilepsy 3 (1-5)195/2256/2198 AEDs if no other trigger
Sleep-disordered breathing 62257 CPAP
Fatigue 40-60223 ? Retraining
Vascular Brain Injury
Mass effects   Neurosurgical decompression
Hydrocephalus Shunting
Catastrophic illness
Depression 16 (12-21)195/26256/13198 CBT ± drugs
Anxiety 14 (10-18)195/8198 CBT ± drugs
Family breakdown   Information + training

AED, antiepileptic drug; CBT, cognitive-behavior therapy; CCF, congestive cardiac failure; CPAP, continuous positive airway pressure; DVT, deep vein thrombosis; GI, gastrointestinal; NG/PEG, nasogastric/percutaneous endoscopic gastrostomy; NSAID, nonsteroidal anti-inflammatory drug; PE, pulmonary embolism.

Until about 1995, 20% to 50% of patients after stroke were managed acutely at home in some European countries,19 despite recommendations to the contrary.20 The benefits of stroke unit care and the gradual introduction of thrombolysis and neuroprotective agents are, alone, likely to reduce this percentage dramatically. Furthermore, patients randomly assigned to receive acute care at home after moderately severe stroke (sufficient to cause persistent neurological deficit affecting continence, mobility, and self-care, and necessitating multidisciplinary treatment), rather than to receive care in an acute and rehabilitation stroke unit or a general ward with stroke team support, were significantly more likely at 1 year to be dead or institutionalized (24% versus 14%; P = 0.03) and less likely to be alive without severe disability (85% versus 71%; P = 0.002) than were patients admitted to the stroke unit.21

In their meta-analysis of 23 trials, the Stroke Unit Trialists’ Collaboration22 compared care in stroke units, nine of which were “comprehensive” and included both acute and rehabilitation components, with care given by alternative services, usually in a general medical or geriatric ward with or without a visiting stroke team. The meta-analysis showed that patients who receive unit-based inpatient care do not stay longer in hospital and are more likely to be alive, independent, and living at home 1 year after the stroke, regardless of gender, age, and stroke severity (Fig. 48-2). Thus, in comparison with alternative services, stroke unit care produced reductions in the odds of death at 1 year (odds ratio, 0.86; 95% confidence interval, 0.71 to 0.94; P = 0.005), of death or institutionalized care (odds ratio, 0.80; 95% confidence interval, 0.71 to 0.90; P = 0.0002), and of death or dependency (odds ratio, 0.78; 95% confidence interval, 0.68 to 0.89; P = 0.0003).

A subsequent systematic review of results from nine postacute units, which admitted patients more than 1 week after stroke, in comparison with an alternative service, revealed benefits similar to those resulting from combined acute and postacute units,23 and in the United States, compliance with postacute but not acute stroke unit guidelines (Table 48-3) has been shown to be correlated with outcome.16 Secondary analysis has indicated that the reduction in stroke unit deaths probably results from a reduction in the complications of immobility rather than in neurological or cardiovascular complications. The increased number of patients discharged home from stroke units and the reduced requirement for institutional care were attributable largely to an increase in the number of patients returning home physically independent (Rankin score, 0 to 2), rather than dependent (Rankin score, 3 to 5).24

TABLE 48-3 Dimensions of Acute Rehabilitation after Stroke

Compliance with these dimensions of process during postacute rehabilitation after stroke is correlated with outcome.

After Duncan PW, Horner RD, Reker DM, et al: Adherence to postacute guidelines is associated with functional recovery in stroke. Stroke 2002; 33:167-178.

Langhorne and Pollock25 identified aspects of care common to 11 stroke units, 8 of which included acute care, reporting beneficial effects between 1985 and 2000 in the Stroke Unit Trialists’ Collaboration’s systematic review.22 These included comprehensive medical, nursing, and therapy assessments; integration of nursing care within the multidisciplinary team; early mobilization and treatment of hypoxia, hyperglycemia, and suspected infection; avoidance of urinary catheterization; and formalized goal-oriented multidisciplinary team care, with early discharge planning and education and involvement of caretakers.

Evans and associates26 found that many of these aspects of care were not delivered by a peripatetic specialist stroke team (PSST). They compared care delivered to 304 patients randomly assigned to an acute and rehabilitation stroke unit (n = 152) or to general wards supported by a PSST (n = 152). Patients in the stroke unit were monitored more frequently, and more of those patients received oxygen, antipyretics, measures to reduce aspiration, and early nutrition than those in general wards. Many aspects of multidisciplinary care occurred more frequently in the stroke unit, in which complications including stroke progression, chest infections, and dehydration were less frequent. Early feeding, stroke unit management, frequency of complications, and measures to prevent aspiration independently affected outcome. In 1984, a PSST’s input to general ward care was shown to nonsignificantly reduce mortality rates and significantly improve functional recovery in men.27 More recently, in a head-to-head comparison at 1 year of patients randomly assigned to receive care from the PSST with those receiving care in a combined acute and rehabilitation stroke unit, more patients in the PSST group were dead or institutionalized (30% versus 14%; P < 0.001) and fewer were alive without severe disability (66% versus 85%; P < 0.001).21 Retrospective data collected by van der Walt and colleagues28 before and 2 years after the introduction of a PSST to a general ward showed significant improvements in prophylaxis for deep vein thrombosis, incontinence management, premorbid function documentation, frequent neurological observations, and early occupational therapy, with fewer severe complications (9% after versus 24% before; P = 0.004), reduced median length of stay (12.0 after versus 18.5 days before; P = 0.003), and more patients independent at discharge (32% after versus 9% before; P < 0.001). It is thus possible that practice developed in stroke units can now be delivered more effectively by a PSST, and further comparison of these two methods of service delivery remains legitimate.

More recently, high-dependency care has been introduced immediately after stroke, providing continuous rather than manual monitoring for hypoxia, hyperglycemia, hypotension, cardiac arrhythmias, and elevated body temperature during the first 48 to 72 hours after admission.29,30 Currently, its effectiveness is relatively unexplored, but there is a suggestion that it may reduce mortality rates at 3 months and 1 year among patients with severe stroke, without increasing dependency.31,32

Remarkably, the differences between stroke unit and alternative care persist for many years. Indredavik and colleagues33 found that even 10 years after random assignment to an acute and rehabilitation stroke unit or a general ward, fewer patients in the stroke unit had died (75.5% versus 87.3%; P = 0.008), more were at home (19.1% versus 8.2%; P = 0.018), and more were at least partly independent with a Barthel Index score of 60 or higher (20.0% versus 8.2%; P = 0.012) or independent with a Barthel Index score of 95 or higher (12.7% versus 5.4%; P = 0.061). Increased survival times 5 years after random assignment to a stroke rehabilitation unit, versus a general medical or geriatric ward, were also reported by Lincoln and colleagues.34

Early discharge, supported by a multidisciplinary outreach team, of medically stable patients after mild and moderate stroke, with an admission Barthel Index score of more than 9, supplements initial stroke unit gains. A meta-analysis of individual patient data from 11 trials of early supported discharge versus conventional care showed that the patients with early supported discharge had a reduced risk of death or dependency (odds ratio, 0.79; 95% confidence interval, 0.64 to 0.97; P = 0.02), a hospital stay shortened by 8 days (P < 0.0001), and significant improvement in extended activities of daily living (P = 0.05), although not in subjective health status or mood in either patients or caretakers. Patients were moderately disabled at discharge with a median discharge Barthel Index score of 15.35 One study revealed that these gains can include better life quality, assessed by the Nottingham Health Profile, at 1 year,36 and another study revealed that gains in domestic and extended activities of daily living are still evident after 5 years.37

Once in the community, patients are known to be at risk of deteriorating as a result of multiple health problems, including falls, depression, and physical and social inactivity and isolation, in addition to age-related symptoms and comorbidity, and health-related quality of life has been shown to significantly decline in the 6 months after discharge.38 Nursing home care does not substitute for stroke unit care,39 but the place for and the optimal process in other service systems for patients later after stroke (e.g., nurse-led wards, nursing homes, or residential placements) remain to be examined.

A meta-analysis of trials of therapy-based outpatient or domiciliary rehabilitation, delivered by either a multidisciplinary team or by a physiotherapist or occupational therapist, with the goal of improving task-oriented behaviors, has shown that deterioration is prevented (odds ratio, 0.72; 95% confidence interval, 0.57 to 0.92; P = 0.009) and dependency in personal care reduced (95% confidence interval, 0.02 to 0.25; P = 0.02).40 The effective components and best location for this type of service need further exploration, but benefit has been consistent in trials of community-based occupational therapy, which have provided sufficient data for a meta-analysis of eight trials that showed that intervention was associated with improved personal, extended, and leisure-based activities of daily living, depending on the intervention target.41 These findings were confirmed in a more wide-ranging systematic review of occupational therapy for stroke patients by Steultjens and associates,42 who also noted the need for further studies of the effectiveness of splinting.

Most studies of physiotherapy in patients in the community after stroke investigate the effect of a particular physiotherapy treatment on upper or lower limb function at the level of impairment and mobility, which may improve, rather than on limitations in activity and independence, which, if examined, may not improve. Domiciliary physiotherapy within 6 months after stroke has been shown to reduce probability of readmission after an average of only 2.9 (range, 1 to 8) visits43 and to reduce dependency at less cost than for day hospital attendance.44,45 In patients more than 1 year after stroke, only four to five physiotherapy sessions produced a clinically small but significant improvement in mobility.46

Informal caretakers should be recognized as an important resource: They enable patients to remain in the community,47 their support is likely to facilitate patient outcomes,48 and depression is more severe in caretakers who feel poorly supported.49 Formal support for caretakers is difficult to obtain in the United Kingdom. Trials of psychosocial interventions to support caretakers of patients with stroke, involving information packages, specialist nurses, a mental health worker, or family support workers, have failed to show functional or psychological benefit in patients and only modest psychosocial benefit for caretakers.5057 In contrast, there is evidence that caretaker adjustment is increased by education and counseling or by training in social problem-solving skills.58 Kalra and colleagues59,60 demonstrated that training informal caretakers in basic nursing skills and facilitation of personal care techniques reduced costs and caregiver burden and improved psychosocial outcomes for the caretaker and the patient, although there was still no change in patients’ rates of mortality, institutionalization, and disability.

MANAGEMENT OF NEUROLOGICAL IMPAIRMENTS

Evidence of dysphagia, with consequent risk of dehydration, further malnutrition, and chest infections resulting from aspiration, has been reported to occur clinically in about 50% of all patients with stroke admitted to a hospital, with videofluoroscopic evidence of a swallowing abnormality in up to 65% of patients and of aspiration in about 20%.61,62 Videofluoroscopic and flexible endoscopic evaluation of swallowing increase the reliability with which aspiration can be identified63,64 when clinicians select which patients need tube feeding. However, whether other aspects of dysphagia management, including dietary modification and compensatory swallowing techniques, reduce the need for tube feeding or the risk of aspiration pneumonia remains unclear despite assertion to the contrary.65 The Feed or Ordinary Diet (FOOD) trials66 revealed that in 859 patients randomly assigned to receive nasogastric feeding within a week, in contrast to more than a week, after stroke, absolute mortality rates were reduced by 5.8% (95% confidence interval, −0.8 to 12.5; P = 0.09) in the group fed early; in 321 patients randomly assigned to undergo percutaneous enteral gastrostomy (PEG) feeding or nasogastric tube feeding a median of 1 week after stroke, PEG feeding was associated with an absolute increase in risk of death of 1.0% (95% confidence interval, −10.0 to 11.9; P = 0.9) and an increased risk of death or other poor outcome of 7.8% (95% confidence interval, 0.0 to 15.5; P = 0.05). Thus, as is recommended current practice in hospitalized adult patients in general,67 nasogastric feeding should be used for dysphagic patients soon after stroke, whereas PEG feeding is reserved for patients who do not tolerate nasogastric feeding and as required in the longer-term care of dysphagic patients.

After stroke, early incontinence is predictive of poor outcomes, including death, lengthy hospital stay, institutionalization, and severe disability.68 New urinary incontinence occurs in 40% to 50% of patients during the first week after admission and in 10% to 20% by 6-month follow-up68,69; it appears to remain at this level in the community over the long term.70 The proportions of stroke patients with new fecal incontinence on admission and at 6-month follow-up are lower, at 30% to 40% and 5% to 10%, respectively.68,69 Causes and predictors68,71,72 of fecal and urinary incontinence include age; stroke type and severity; “functional incontinence” resulting from stroke-related cognitive and communication difficulties and mobility problems; autonomic neuropathies, usually diabetic in origin; medications causing bladder and bowel hyporeflexia; preexisting bladder outflow obstruction in men or stress incontinence in women; and perhaps depression and lowered self-esteem that result from the incontinence itself.73,74

Current guidelines (e.g., Royal College of Physicians12) for the management of incontinence after stroke recommend initial definition of its cause and associations through a full clinical assessment. The neurogenic cause after stroke is usually disruption of suprapontine inhibition of bladder contractility resulting in detrusor hyperreflexia, but bladder hyporeflexia may occur after cerebellar stroke.75 Evidence for the effectiveness of methods promoting continence after stroke is currently derived largely from trials in other (nonstroke) patient groups. Management of urinary incontinence76 includes a combination of anticholinergic drug therapy, bladder training by prompted and/or timed voiding77,78 or biofeedback,79 and appropriate management of outflow obstruction and stress incontinence, for which one small study of 26 stroke patients randomly assigned to receive treatment or to control conditions showed no benefit from a 12-week pelvic floor muscle training program.80 Similar general principles apply to the management of fecal incontinence,81 which in inpatients or in discharged patients is associated with needing help to use the toilet82 and thus might be addressed by improving functional independence, whereas constipation but not fecal incontinence after stroke is improved by a single clinical/educational nurse intervention up to 6 months later.83

Impairment of trunk control and sitting balance after acute stroke is common, and recovery is a reliable predictor of functional outcome after stroke. Trunk control, measured by the trunk control test at rehabilitation admission a median of 5 weeks after stroke, accounted for 71% of the variance of the motor component of the Functional Independence Measure at discharge 10 weeks after stroke84; as measured by the Postural Assessment Scale for Stroke Patients within 2 weeks after stroke, trunk control was strongly correlated with functional outcome, rated by a combined score of both personal (Barthel Index) and instrumental (Frenchay Activities Index) activities of daily living at 6 months after stroke.85 A positive correlation has also been found between sitting balance and the Barthel Index score86 and between sitting balance and gait at 6 months.87 Mudie and associates88 found that three specific treatment approaches implemented early after stroke improved sitting balance in the short term in comparison with a nonspecific control approach. Whether early targeting of sitting balance for treatment could improve mobility over the long term is an interesting question that remains to be explored.

Disordered motor control of the limbs after stroke is usually caused by the positive and negative effects of the upper motor neuron syndrome, in which the central abnormality is usually muscle weakness and co-contraction resulting from a failure of coordinated high-frequency motor neuron firing during movement, rather than high tone resulting from spasticity and contracture found at rest,89 which is seen clinically in only 20% to 30% of hemiparetic patients 3 to 12 months after stroke.90,91 Spasticity at rest, when it is a velocity-dependent increase in tonic stretch reflexes with exaggerated tendon jerks, is of diagnostic use but does not contribute significantly to impairment during active voluntary movement and function in either the leg or the arm92,93 and is only one factor contributing to increased muscle tone in the upper motor neuron syndrome, in which co-contraction and biomechanical changes contribute significantly to the resistance to passive movement.94 It has thus been easier to show that pharmacological treatments that reduce the hypertonus of spasticity and co-contraction benefit passive rather than active functional activities, including hand and perineal hygiene, dressing, pain, and limb position,95100 and even correction of equinovarus at the ankle to improve weight bearing by the affected leg is unlikely to translate into functional improvements in gait101,102 unless it is followed by physical measures to reduce soft tissue shortening and a program of task-related training.103,104

Thus, although treatments for spasticity after stroke achieve passive functional goals by preventing contracture or reduce pain and are of particular value in dependent patients unable to participate in skill learning, the results of treatments for spasticity in general and after stroke have emphasized the fundamental truth of Landau’s statement in 1974105 that “If the major disability of the upper motor neuron syndrome is due to diminished neural input to segmental control of the final common path (negative symptoms), it follows that only some method of provoking [central nervous system] neuronal regeneration or of improving the potency of and control by surviving upper level neurons could provide a direct remedy.” Landau’s next sentence was “No such approach is on the horizon,” and at that time the focus in rehabilitation was on training in compensatory strategies and social and environmental modification. Since the mid-1990s, however, there have been investigations of neurobiological rehabilitation strategies designed to modify the neural processes and behaviors that occur during recovery (Fig. 48-3) (Dobkin, 2004).106

image

Figure 48-3 Both patient A and patient B suffered a stroke affecting the right hand. The T1-weighted magnetic resonance imaging scans on the left (“infarct”) demonstrate that patient A suffered a left pontine infarction and patient B suffered a left middle cerebral artery territory infarction. The five scans to the right of each structural scan show patterns of brain activation, measured with functional magnetic resonance imaging, during repetitive gripping with the affected right hand at different time points over the first 3 months after stroke. (The brain is seen from above, with the anterior aspect at the top of the image.) Recovery of function in patient A is associated with early widespread activation within recognized motor related areas, followed by a gradual focusing toward a normal lateralized pattern; the 3-month (far right) scan shows activity confined largely to the left sensorimotor cortex, as in normal subjects. Recovery of function in patient B is also associated with focusing of the early pattern of widespread activation, but in this instance activity focuses toward the right sensorimotor cortex, ipsilateral to the affected hand. Ipsilateral sensorimotor cortex activation is rarely seen in normal subjects. This focusing is due to increasingly efficient neural circuitry, very similar to that seen during learning of a new complex motor task in the undamaged human brain. However, it is possible to focus only onto regions of the brain that can still generate a motor output signal. In the case of patient B, many of the left hemisphere cortical motor regions have been disconnected by the infarct. Thus, there appears to be a reliance on right motor cortex to generate right hand movements. This “secondary” system is necessarily less efficient, and this is reflected in less complete recovery of patient B in comparison with patient A (hand grip of 64% of the unaffected side for patient B at 3 months, in comparison with 89% for patient A). This finding suggests two important consequences: (1) It ought to be possible to use therapies that are designed to drive this process toward the optimally configured motor system and (2) it helps clinicians appreciate that damage to brain structures is likely to be a major constraint to this process and that reorganization can take place only in surviving brain regions; this has implications about how much recovery can be expected.

Meta-analyses of physiotherapy after stroke have revealed significant improvements in independence in activities of daily living and reduction in impairments with higher intensities of physiotherapy.107109 Traditional physiotherapeutic strategies emphasize cutaneous and proprioceptive stimulation, reduction of tone, and therapist-induced central facilitation of normal movement, rather than voluntary activation of proximal or distal musculature to relearn functional tasks. This type of task-related motor relearning was first shown to be effective in improving the ability to balance during seated reaching activities late after stroke.110 Although this approach has not yet been consistently shown to improve functional outcomes and resource use early after stroke,111,112 its principles of repetition, task orientation, attention, and reward are similar to those that result in motor learning and cortical neural reorganization in nonhuman primates with and without ischemic cortical damage.113 It is thus a “neurobiological” approach to skill relearning in which repetition of graded and motivating task-related learning programs is envisaged to drive the acquisition of motor, linguistic, and cognitive skills and more complex behaviors through activity-dependent neural reorganization, regrowth, and replacement.114

Although these techniques can be shown to produce neuroplastic effects—in humans, usually by functional imaging techniques—these changes should not be confused with the potential clinical usefulness of these techniques, which requires a robust behavioral effect if measurable functional benefit is to occur. The effects of task-related training are seen most obviously in the function targeted for treatment; change has been demonstrated after stroke in upper and lower limb function and linguistic skills. Factors that optimize skill learning, including implicit rather than explicit feedback115 and a random rather than blocked learning schedule,116 are likely to affect the rate at which a task is learned and the extent of carryover into novel environments. In the arm, training is focused on practicing graded motivating functional tasks, including grasping, reaching, leaning, and manipulating clothing by the affected limb; in the trunk and leg, training is focused on the recovery of bed mobility, sitting and standing balance, transfers, gait stability and velocity, and stair climbing. Kwakkel and colleagues117 showed that leg training of this sort for an average of 30 minutes of therapy 5 days a week for 20 weeks after stroke onset, in contrast to immobilization of the limb in an inflatable cuff for a similar time, increased performance in activities of daily living (measured by the Barthel Index), walking ability, and also hand dexterity, whereas arm training increased arm dexterity alone.

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