Literature DB >> 27752057

Movement repetitions in physical and occupational therapy during spinal cord injury rehabilitation.

D Zbogar1,2,3, J J Eng1,2,3, W C Miller1,2,4, A V Krassioukov2,5, M C Verrier6,7.   

Abstract

STUDY
DESIGN: Longitudinal observational study.
OBJECTIVE: To quantify the amount of upper- and lower-extremity movement repetitions (that is, voluntary movements as part of a functional task or specific motion) occurring during inpatient spinal cord injury (SCI), physical (PT) and occupational therapy (OT), and examine changes over the inpatient rehabilitation stay.
SETTING: Two stand-alone inpatient SCI rehabilitation centers.
METHODS: Participants: A total of 103 patients were recruited through consecutive admissions to SCI rehabilitation.
INTERVENTIONS: Trained assistants observed therapy sessions and obtained clinical outcome measures in the second week following admission and in the second to last week before discharge. MAIN OUTCOME MEASURES: PT and OT time, upper- and lower-extremity repetitions and changes in these outcomes over the course of rehabilitation stay.
RESULTS: We observed 561 PT and 347 OT sessions. Therapeutic time comprised two-thirds of total therapy time. Summed over PT and OT, the median upper-extremity repetitions in patients with paraplegia were 7 repetitions and in patients with tetraplegia, 42 repetitions. Lower-extremity repetitions and steps primarily occurred in ambulatory patients and amounted to 218 and 115, respectively (summed over PT and OT sessions at discharge). Wilcoxon-signed rank tests revealed that most repetition variables did not change significantly over the inpatient rehabilitation stay. In contrast, clinical outcomes for the arm and leg improved over this time period.
CONCLUSIONS: Repetitions of upper- and lower-extremity movements are markedly low during PT and OT sessions. Despite improvements in clinical outcomes, there was no significant increase in movement repetitions over the course of inpatient rehabilitation stay.

Entities:  

Mesh:

Year:  2016        PMID: 27752057      PMCID: PMC5292050          DOI: 10.1038/sc.2016.129

Source DB:  PubMed          Journal:  Spinal Cord        ISSN: 1362-4393            Impact factor:   2.772


INTRODUCTION

Occupational therapy (OT) and physical therapy (PT) play a central role in the rehabilitation of individuals who have experienced a spinal cord injury (SCI). Over the past several years, quantifying therapy content in SCI rehabilitation has received increasing attention in order to better understand current practice. The SCIRehab project is a notable comprehensive and recent example[1] where therapists recorded the number of sessions, minutes, activity-specific details, and the extent of patient participation in PT[2] and OT[3] sessions in inpatient rehabilitation. While studies of content and time spent on activities[4-8] provide a key component to unraveling the relationship between therapeutic intervention and outcomes, they do not provide an indication of the amount of active therapist directed movement repetitions during that time, which are important for optimizing neuroplasticity. Research studies in animals and humans have found that remodeling in the nervous system accompanies the practice of motor tasks after SCI and can facilitate the recovery of locomotor function[9] and reaching.[10] In patients with incomplete SCI, rehabilitation therapies such as repetitive upper extremity movements improve hand function,[11,12] while locomotor training promotes ambulatory recovery.[13] However, improved locomotor capacity after SCI in the animal literature involves several hundred to over a thousand repetitions[14,15] with higher doses resulting in improved outcomes. Overall, the animal and human motor learning literature support repetitions in the mid-hundreds to thousands to show improvement in upper or lower extremity measures.[11-15] Measuring repetitions is also important as it forms a basis for task-specific practice, as well as muscle conditioning to ultimately facilitate functional outcomes. For example, repetitions of movements involving the arms may strengthen the arms and help learn correct movements to reduce the increased potential for musculoskeletal injury that results from propelling a manual wheelchair or performing transfers, whether the individual has tetraplegia or paraplegia with neurologically intact upper extremities. Unfortunately, there are no reports that estimate the movement repetitions during human SCI rehabilitation, and thus, we do not know whether patients are receiving sufficient repetitions to optimize their rehabilitation. This study will fill this gap by measuring movement repetitions during inpatient SCI rehabilitation. Research evidence suggests the weeks (animal studies) and months (human studies) following a SCI are a critical time window for optimizing recovery,[16-19] when the central nervous system is more sensitive to stimuli and experience, including exercise in the form of repetitive practice of voluntary movements. This time generally corresponds to the sub-acute inpatient rehabilitation stay. Due to the SCI itself, any accompanying injuries, prolonged bed-rest, and a host of psychological sequelae, it is expected that patients may tolerate a small number of repetitions early in rehabilitation, but progress over time to challenge the neurological and musculoskeletal systems Thus, knowing the current repetitions of activities during this period of rehabilitation and how they progress over time will provide a baseline of activity levels and set the stage for clinical trials aimed at developing interventions to enhance neurological recovery, as well as improve functional outcomes. Thus, knowing the current repetitions of activities during this period of rehabilitation and how they progress over time will provide a baseline of activity levels and set the stage for clinical trials aimed at developing interventions to enhance motor learning and improve rehabilitation outcomes. Our aims were to 1) quantify the amount of movement repetitions (active therapist directed movement repetitions involving voluntary movements) that patients experience for the upper extremity and lower extremity during inpatient SCI rehabilitation, and 2) quantify changes in the amount of movement repetitions that patients with SCI undertake over their time in rehabilitation. To investigate our questions we completed the first study to observe PT and OT sessions and collected information on the amount of repetitions, type of activity, and time spent on activities during inpatient SCI rehabilitation. We expected that movement repetitions would increase for PT and OT sessions over the SCI inpatient rehabilitation stay, commensurate with improvements in patient function. We also expected that movement repetitions for both the upper and lower extremity would be low during PT and OT sessions.

METHODS

Participants

Patients with traumatic and non-traumatic SCI were recruited from consecutive admissions to inpatient subacute care at two stand-alone rehabilitation centres from November 2010 to December 2012. Non-traumatic SCI was defined as that resulting from spinal stenosis, tumor, ischemia, transverse myelitis, and infection.[20] Ambulatory participants were defined as those who were independently ambulatory (with or without assistive devices) at the time of the discharge assessment. Patients were excluded if they had a traumatic brain injury that significantly affected content and delivery of therapy or if their length of stay in rehabilitation was projected to be less than four weeks as it precluded the ability to collect admission and discharge data. Approval for this study was obtained from the university research ethics boards. All observed patients and therapists provided informed consent prior to therapy observation.

Observed therapy sessions

A trained observer recorded all activities that a patient performed, occurring under the direction of a physical therapist, occupational therapist, or rehabilitation assistant. The observations most often included PT and OT sessions, but also included supplementary sessions with rehabilitation assistants occurring in the rehabilitation area and on the ward. As we wanted to measure typical active therapy sessions, the first measurement occurred in the second week after admission to avoid observation of sessions involving assessments. Observers recorded all PT and OT therapy activities that occurred on two days within that week period. The final measurement took place in the second-last week before discharge to avoid discharge planning and re-assessment activities. Again, two days within that week were observed. While patients were assessed at different times post-injury, our choice of measurement time is a clinically relevant option as it uses specific criteria for admission to inpatient rehabilitation services and ensures that patients are ready to be engaged in intensive rehabilitation activities. To be admitted for inpatient rehabilitation from acute care, patients must: be medically stable and would benefit from a short-stay interdisciplinary rehab program, be able to follow simple commands, be able to learn and recall enough information from day-to-day in order to participate, have identified specified rehab goals that are attainable, and have adequate cognition, motivation, behaviour and endurance to benefit from an intensive rehabilitation program. Criteria for discharge from inpatient services includes having achieved goals for inpatient rehabilitation, the patient no longer making any functional gains, the patient refusing to participate in active rehabilitation, or they are medically unstable. Therapy sessions were included for observation if more than 50% of therapeutic time was comprised of physical rehabilitation. Therapeutic time was defined as any activity undertaken by the therapist with the goal of treating the patient and included physical rehabilitation, education, assessments, and interventions designed to improve functional independence. Sessions were excluded if more than 50% of therapeutic time was comprised of admission or discharge assessments, equipment fitting, or non-motor issues (e.g. discharge planning, education). Thus, our criteria allowed us to assess therapeutic repetitions under a best-case scenario, and omitting sessions not representative of the majority of therapy sessions. Non-therapeutic time was defined as any activity that occurred but was not for treating the patient’s condition, such as talking, resting, changing location, or setting up for the next activity. If a session did not occur on a scheduled day or did not meet the criteria indicated above, an additional day of therapy was observed if it occurred within one-week of the first day of data collection. Standardization between trained and new observers was accomplished by an orientation where new observers were familiarized with the data collection protocol and then recorded sessions with an experienced observer. The lead investigator and the observer compared therapy observation data sheets following therapy sessions, feedback was provided, and further sessions were recorded under supervision until the data recorded were at ≥95% agreement. In addition to the lead investigator, 4 individuals (1 physical therapist, 3 research assistants) observed therapy sessions over the course of the study. During observed therapy sessions, the observer situated themselves such that they were able to clearly see and hear the therapy session while being a distance away such that their presence did not interfere with therapy delivery. Moreover, observers did not engage the therapist or patient during the session. To record information, the observer used a stopwatch and data collection sheets to document the type of therapy (PT or OT), repetitions, movement classification, and duration of activity. Movements were classified via a taxonomy (Table 1) modified from others.[21-23] The categories used in this study included: upper extremity (including all arm and hand movements), hand (a subset including only repetitions of the hand/wrist), lower extremity (including all lower extremity activity), and stepping (a subset of lower extremity including only stepping on flat surfaces or ascending/descending stairs). As we wished to include only those repetitions that contributed most to motor and functional recovery (Tables 3, 4 and 5), we excluded passive movements.
Table 1

Definitions of Movements, Units of Repetition, and Examples for Categories and Subcategories

Category
Definition
Definition of a single repetition
Examples
Upper Extremity
 TotalAny movement in which the patient attempted to or moved the upper limb through a specific motion or attempted or accomplished a functional taskOne movement of 1 limb from initial position and back again OR one movement from initial position to desired position OR One movement from one surface to another using the armsDumbbell exercises, pulley exercises using the arm, transfers, mobility
 Hand onlyAny movement in which the patient attempted or moved the finger(s) or wrist through a specific motionOne movement from initial position and back againworking on grip/dexterity, wrist roller, squeezing ball, pegboard
Lower Extremity
 TotalAny movement in which the patient attempted or moved the lower limb through a specific motionOne movement of 1 limb from initial position and back againHip abduction; knee extension; hamstring curl, balance training
 GaitWalking overground or on a treadmill; going up and/or down stairsEach step of each footwalking
Table 3

Clinical outcome measures at admission and discharge from inpatient SCI rehabilitation

Variable
Admission
Discharge††
95% CI
Paraplegia

Grip strength, (kg)34.8±13.535.3±13.5−2.3, 1.3
SCIM III- Total50.7±17.066.6±17.1−19.2, −12.6
Tetraplegia

Grip strength, (kg)6.4±10.69.7±10.9−5.4, −1.3
GRASSP64.0±35.977.7±34.9−19.2, −8.3
SCIM III- Total32.7±23.852.3±27.8−24.6, −14.6
Ambulatory Patients

10MWT- comfortable, (m/s)0.30±0.400.76±0.37−0.6, −0.4
WISCI II6.4±7.915.5±5.3−11.5, −6.7
SCIM III- Total57.0±21.078.6±12.8−26.8, −16.5

Second week after admission;

Second week before discharge; All values are means±SD; CI= confidence interval; 10MWT= 10 Meter Walk Test; WISCI II= Walking Index for Spinal Cord Injury II; SCIM III= Spinal Cord Independence Measure III.

Table 4

Patients with paraplegia: Therapy time and repetitions at admission and discharge from inpatient SCI rehabilitation.

Variable
Admission
Discharge††
Z value
p
r
Physical Therapy (n=55)

Total time (min)54, 45–5953, 37–62−0.5990.55−0.06
Therapeutic time (min)32, 24–3933, 22–41−0.360.72−0.03
Upper extremity (reps)7, 0–559, 0–34−0.9060.37−0.09
Lower extremity (reps)30, 0–15550, 0–230−1.9320.053−0.18
Occupational Therapy (n=49)

Total time (min)34, 12–480, 0–31−3.4750.001*−0.35
Therapeutic time (min)17, 7–250, 0–17−3.3350.001*−0.34
Upper extremity (reps)0, 0–40, 0–0−1.6340.10−0.17
Lower extremity (reps)0, 0–00, 0–0−0.7340.46−0.07

Second week after admission;

Second week before discharge; All values are median, Q1–Q3;

p ≤ 0.008 (Benjamini-Hochberg corrected significance level); r= effect size; n= number of patients.

Table 5

Patients with tetraplegia: Therapy time and repetitions at admission and discharge from inpatient SCI rehabilitation.

Variable
Admission
Discharge††
Z value
p
r
Physical Therapy (n=48)

Total time (min)53, 44–6252, 37–62−0.4620.64−0.05
Therapeutic time (min)31, 23–3831, 24–43−1.5380.12−0.16
Upper extremity (reps)11, 0–5313, 0–68−1.1380.26−0.12
Hand (reps)0, 0–00, 0–0−0.6740.50−0.07
Lower extremity (reps)13, 0–12733, 0–215−0.8330.41−0.09
Occupational Therapy (n=43)

Total time (min)44, 26–5430, 0–46−2.2850.022−0.25
Therapeutic time (min)27, 13–3518, 0–31−2.50.012−0.27
Upper extremity (reps)31, 0–1272, 0–34−2.9650.003*−0.32
Hand (reps)7, 0–570, 0–15−3.1160.002*−0.34
Lower extremity (reps)0, 0–00, 0–0−0.1690.87−0.02

Second week after admission;

Second week before discharge; All values are median, Q1–Q3;

p ≤ 0.008 (Benjamini-Hochberg corrected significance level); r= effect size; n= number of patients.

On the occasion that the patient was undergoing two therapeutic activities at the same time (e.g., simultaneous upper and lower extremity repetitions), both movements were recorded and included as therapeutic activities. In calculating therapeutic time in a session, we subtracted non-therapeutic time (e.g., resting) from total therapy time to avoid the possibility of therapeutic time being longer than the actual session time. Outside of therapy observation, patients were asked how many minutes of structured group classes they attended that day. These classes were not observed as patients were not followed outside of individual PT and OT therapy sessions. Group classes included wheelchair skills, pulleys (upper body), and hand function.

Clinical outcome measures

Clinical outcome measures were collected on a separate day within the admission and discharge data collection periods. The Spinal Cord Independence Measure measures the ability of SCI patients to accomplish ADLs in the area of self-care, respiration and sphincter management, and mobility,[24] and is scored from 0–100 with higher scores indicating better functional independence. The measure has excellent validity and reliability.[25] Ambulatory patients were assessed with the Walking Index for SCI II, designed to gauge ambulation over a 10-meter distance with ambulation aids and physical assistance. Locomotor ability is assessed on a 0 to 20 hierarchical scale where a lower number indicates higher impairment. This assessment shows excellent reliability and validity.[26] Grip strength was tested using a hand-held Jamar Dynamometer (Nicholas MMT, Lafayette Instrument, Lafayette, IN). Patients performed three maximal voluntary contractions, with at least 30 seconds of rest between trials. The trials were averaged to obtain a mean score in kilograms. Measurements were taken with the patient seated, the elbow bent at 90 degrees, and hand in a neutral position. This test is reliable and valid for assessing grip in healthy and hand-injured populations.[27,28] The Graded Redefined Assessment of Strength, Sensibility and Prehension was used with patients with tetraplegia to evaluate muscle, sensory, and grasping function. This assessment involves scoring six functional tasks and assessing upper extremity strength and sensibility (i.e., perception of sensation) of the hands; scores for each hand are summed (0 to116) with higher scores indicating better hand function.[29] The assessment has demonstrated reliability and validity in the SCI population.[30] Demographic information was collected for age, gender, injury level (paraplegia/tetraplegia), ASIA Impairment Scale score, aetiology (traumatic or non-traumatic), and length of stay in acute care and rehabilitation.

Data analysis

For OT and PT, therapy time and repetitions were calculated by averaging sessions occurring over two days to obtain a daily therapy value. Descriptive statistics for patient demographics are included in Table 2. Clinical outcome measures are presented in Table 3 and the therapeutic time and movement repetition data for patients with paraplegia and tetraplegia is presented in Tables 4 and 5, respectively. We also provide descriptive data for the tetraplegia group separated by complete and incomplete SCI status (Table 6), but this data is not assessed statistically due to the small size of these subsets and overlap with other analyses. Additionally, we present data for those patients able to ambulate by the time of their discharge assessment because it is likely that their therapy sessions involved ambulatory goals and activities (Table 7). Wilcoxon signed rank tests determined whether therapy times (total time, therapeutic time) and movement repetitions (total upper extremity, hand, total lower extremity, steps) changed over the rehabilitation stay from admission to discharge; Z value and effect size (r) are documented (small effect size = 0.1; medium effect size = 0.3; large effect size = 0.5[31]). For clinical outcome measures, means, standard deviations, and confidence intervals for admission and discharge are documented. As defined by Cohen,[32] a small effect size was 0.01, a medium effect size was 0.06 and a large effect size was 0.14.
Table 2

Demographic and SCI Information for All Patients and Subgroups of Paraplegia and Tetraplegia and Ambulatory Patients

Variable
All Patients
Paraplegia
Tetraplegia
Ambulatory
n103554845
Gender (M/F)75/28 (73/27)38/17 (69/31)37/11 (77/23)33/12 (73/27)
Traumatic/nontraumatic68/35 (66/34)32/23 (58/42)36/12 (75/25)28/17 (62/38)
ASIA AIS, (A/B/C/D)††23/12/12/56 (22/12/12/54)12/6/9/28 (22/11/16/51)11/6/3/28 (23/13/6/58)1/2/0/42 (2/4/0/93)
Age, years49±17, 53, 6948±18, 52, 6850±17, 53, 6050±16, 54, 66
LOS in rehabilitation, days96±46, 93, 22585±38, 76, 224110±51, 116, 21576±43, 65, 215
LOS in acute care, days38±38, 23, 17032±33, 20, 15446±43, 30, 16520±13, 16, 54

Values are n(%) or mean±SD, median, range; n= number of patients; ASIA= American Spinal Injury Association; AIS= ASIA Impairment Scale; LOS= Length Of Stay;

The Ambulatory group is composed of a subset of individuals from Paraplegia and Tetraplegia who were able to ambulate by the time of the discharge assessment;

While the AIS is valid for traumatic SCI, it has not been validated in non-traumatic SCI.

Table 6

Patients with tetraplegia: Therapy time and repetitions separating for motor complete and motor incomplete injury.

Variable
Complete
Incomplete
AdmissionDischarge††AdmissionDischarge††



Physical Therapy

n1731
Total time (min)52, 45–6154, 44–6654, 43–6350, 34–62
Therapeutic time (min)26, 23–3732, 24–3933, 22–4130, 24–44
Upper extremity (reps)23, 0–11036, 0–11911, 0–281, 0–44
Hand (reps)0, 0–00, 0–00, 0–00, 0–0
Lower extremity (reps)0, 0–00, 0–082, 21–207145, 34–342
Occupational Therapy

n1627
Total time (min)28, 15–4923, 0–4445, 35–5637, 12–46
Therapeutic time (min)15, 7–2412, 0–2230, 24–4322, 9–34
Upper extremity (reps)0, 0–190, 0–1081, 15–17223, 0–54
Hand (reps)0, 0–00, 0–034, 1–1240, 0–22
Lower extremity (reps)0, 0–00, 0–00, 0–00, 0–0

Second week after admission;

Second week before discharge; All values are median, Q1–Q3; n= number of patients.

Table 7

Ambulatory patients: Therapy time and repetitions at admission and discharge from inpatient SCI rehabilitation.

Variable
Admission
Discharge††
Z value
p
r
Physical Therapy (n=45)

Total time (min)54, 45–6153, 37–68−0.2140.83−0.02
Therapeutic time (min)35, 26–4238, 26–49−1.8790.060−0.20
Lower extremity (reps)143, 65–300218, 114–381−1.0270.30−0.11
Steps (reps)51, 0–176115, 21–313−1.1910.23−0.13
Occupational Therapy (n=41)

Total time (min)35, 16–4824, 0–45−2.0820.037−0.24
Therapeutic time (min)24, 10–3316, 0–25−2.2420.025−0.25
Lower extremity (reps)0, 0–30, 0–0−0.5340.59−0.06
Steps (reps)0, 0–00, 0–00.01.00.00

Second week after admission;

Second week before discharge; All values are median, Q1–Q3;

p ≤ 0.008 (Benjamini-Hochberg corrected significance level); r= effect size; n= number of patients.

Statistical software, SPSS 17 (SPSS Inc., Chicago, IL USA) was used for the analysis. Given the number of tests employed, a Benjamini-Hochberg calculated alpha was used to correct for multiple comparisons and minimize type I error.[33] Based on the number of comparisons and p-values, a Benjamini-Hochberg alpha value of 0.008 was calculated and utilized. Reported values are medians unless stated otherwise.

RESULTS

Patient demographics and clinical outcomes

A total of 115 patients entered the study from November 2010 to December 2012 (Recruitment information provided in Figure 1). Of these, we attained a discharge evaluation for 103 (90%). While we could not attain a discharge evaluation for 12 patients because they were discharged with insufficient notice, demographic variables for these patients (not reported) were similar to those included for analyses. Demographic information is provided in Table 2. From the 103 patients in this study, we observed 561 PT sessions and 347 OT sessions. Some patients did not engage in any sessions over the observed week that were focused on physical activities and were assigned a value of zero repetitions. This occurred for four patients prior to discharge from PT, for 22 patients after OT admission, and 42 patients prior to OT discharge.
Figure 1

Flow diagram of recruitment to the study

There were clinically meaningful improvements for all clinical outcome measures except grip strength for individuals with paraplegia (Table 3).

Changes in therapy time

Total therapy session time and therapeutic time did not change during PT sessions over the rehabilitation stay, but did during OT sessions for individuals with paraplegia who experienced a reduction in both these variables (Total time: 34 vs. 0 minutes; Therapeutic time: 17 vs. 0 minutes) (Table 4). Total therapy time for PT and OT sessions combined amounted to about 1.5 hours at admission, 1.25 hours at discharge, and on average, 60% of total therapy time was classified as therapeutic time.

Changes in upper extremity repetitions

Total daily upper extremity repetitions can be found in Figure 2. Upper extremity repetitions were primarily undertaken in OT. More specifically, for patients with tetraplegia, upper extremity repetitions decreased significantly from 31 to 2 in OT (Table 5). Hand repetitions (Table 5), a subset of upper extremity repetitions, were low in OT sessions (7 repetitions) and decreased significantly over the rehabilitation stay (0 repetitions). During OT, repetitions were notably higher for tetraplegic individuals with motor incomplete injury (Table 6).
Figure 2

Daily repetitions for physical therapy and occupational therapy combined.

a. Group with paraplegia.

b. Group with tetraplegia.

Values are median and interquartile range

In the subset of individuals with paraplegia (Table 4), upper extremity repetitions were low after admission (7 in PT sessions and negligible in OT sessions) and did not change over the rehabilitation stay.

Changes in lower extremity repetitions

Total daily lower extremity repetitions can be found in Figure 2. Lower extremity repetitions were primarily undertaken in PT. For participants with paraplegia (Table 4) and tetraplegia, (Table 5) lower extremity repetitions did not exceed 30 repetitions after admission in PT but did not change significantly over the rehabilitation stay, and were higher for motor incomplete individuals with tetraplegia (Table 6) and paraplegia compared to those with motor complete injury. For patients who were ambulating by the time of their discharge assessment (Table 7), the values for lower extremity repetitions (143) and steps (151) after admission in PT sessions did not change significantly over the rehabilitation stay.

Participation in group classes

The average time spent in group classes was 12 minutes after admission and 15 minutes prior to discharge.

DISCUSSION

Amount of movement repetitions

Our primary finding is that repetitions are notably low during rehabilitation. Individuals with motor incomplete tetraplegia, who had the highest amount of upper extremity repetitions, did not exceed 100 during PT and OT sessions combined with all other groups not reaching half this amount. Ambulatory individuals, who had the highest amount of lower extremity repetitions and steps, did not exceed 218 and 115 repetitions during combined PT and OT sessions measured at discharge. These repetitions values are markedly lower than that which has been reported to be necessary for optimizing neuroplastic changes.[14,15,34] These repetitions are also low for musculoskeletal or endurance functions. For example, a typical wheeling push frequency is one push per second[35] and the seven upper extremity repetitions (total for PT and OT) measured in our patients with paraplegia would hypothetically allow one to wheel for a fraction of a minute. These repetition levels would not be sufficient to strengthen the upper extremities to prevent overuse injuries or develop upper extremity endurance for wheeling. Similarly, for ambulatory patients, the 115 steps (total for PT and OT) that we observed at the discharge gait speed (0.76 m/s) with a typical short step length (0.5 m) would hypothetically result in only 1.3 minutes of walking practice over 58 metres, which is not sufficient for any community ambulation activity. In the animal literature, movement repetitions are acutely challenged where success rates of only 60% are experienced for reaching tasks[10] and likely contribute to the positive effects of task-specific training.[10,36] We know from observation that the large majority of patients were able to complete all repetitions prescribed. It is possible that individuals with SCI could perform more difficult exercises to improve gains during rehabilitation stay. However it is likely that therapists prescribe exercise that is challenging yet at the same time meets with successful execution since failed repetitions could be demotivating to a patient, and in some activities, potentially injurious.

Changes in movement repetitions

For the most part, little change in repetitions occurred over the rehabilitation stay. This may be attributed, on the one hand, to patients who met their therapeutic goals earlier in their stay and then focused on non-motor activities as they approached discharge time and on the other hand, to patients who were not able or motivated to undertake larger amounts of repetitions over time due to factors such as fatigue, pain, or depressive symptoms. It is also possible that therapists did not provide sufficient time for patients to engage in movement repetitions during therapy and this could be the result of limited time combined with numerous rehabilitation goals outside of practicing movement repetitions. Given that 61% of patients had motor incomplete injuries, it would appear that patients could have benefited from further motor training, but other priorities left little time for these activities. While much neuroplasticity research measures or manipulates intensity through movement repetitions (e.g. number reaches for a food pellet), the reality of inpatient SCI rehabilitation is more complex. In addition to repetitions, the intensity of an activity may be increased by adding a greater load or by selecting a more difficult movement. For example, 30 repetitions may have been done with a 2kg weight after admission and with 5kg prior to discharge. While it is possible that increases in intensity through means other than greater repetitions may hinder the detection of significant differences from admission to discharge, the field of research investigating the role of rehabilitation in neuroplasticity[11-15,34] is dominated by manipulation of dose through repetitions. We have shown that repetitions are low at both time points.

Therapeutic versus non-therapeutic time

It is common for clinical research to use hours of therapy as an independent variable when evaluating outcomes,[2-8] and health-care guidelines often use this metric.[37] However, we found that approximately 40 percent of a session was non-therapeutic time (e.g., sling transfers, setting up the next activity); activities not therapeutic in themselves but necessary for delivering therapy. If appropriate therapeutic guidelines are to be made for public policy decisions, the actual patient time spent engaged in the therapeutic interventions needs to be considered.

Changes in clinical outcomes

Despite repetitions being notably below repetition volumes seen in the human and animal motor learning literature, patients experienced improvements on clinical outcome measures, reflecting a combination of natural recovery and effects from the rehabilitation process. Nevertheless, improvement is not the same as optimization, and the finding that therapy repetitions are vastly lower than task-specific training protocols suggests that methods to increase repetitions would move us towards optimizing clinical outcomes. However, as mentioned earlier, therapy time cannot be solely dedicated to high-repetition task-specific training for gait or reaching as numerous other therapeutic goals such as addressing spastic musculature or pain take up the patient’s time which is already limited as approximately one-third of sessions is spent on non-therapeutic activities (e.g. repositioning) that are necessary for delivering therapy. One alternative which has been successful in the stroke inpatient setting[38,39] is to accumulate repetitions outside of therapy time with the support of caregivers or rehabilitation assistants. The same potential may exist in therapy for individuals with SCI.

Limitations

We did not monitor repetitions that occurred outside of PT and OT directed activities, for example during group classes and activities of daily living. However, group class time was low, with a median (Q1–Q3) value of 0 (0–30) minutes per day; almost 2/3 of individuals did not engage in group classes during measurement days. Also it is likely that the active time was less, given the nature of group classes being more social, and set up time required for multiple participants. While nine persons with concomitant TBI were included, we excluded four individuals with severe traumatic brain injury whose therapy had a focus on cognitive, rather than physical rehabilitation. We also excluded nine individuals with a length of stay shorter than four weeks. While the number of participants who were excluded for these reasons is small, this may limit how well our sample represents the true breadth of the clinical presentation of SCI. It is possible that social desirability bias resulted in the therapists undertaking more repetitions that usual. We believe we minimized this risk as therapists were specifically asked to deliver therapy as they ordinarily would and to not involve or communicate with the observer during the observed session. Additionally, it is difficult to conceive that therapists would change their practice for the 2 years that data was being collected.

CONCLUSION

The amount of movement practice that occurs during inpatient SCI therapy is notably low, and does not appear to progress over time. The implication is that the stimuli applied during inpatient stay may not be adequate to maximize the musculoskeletal or neural changes needed to promote optimal function after SCI. We recommend that future research investigate patient perception of physical activity intensity during rehabilitation.
  35 in total

Review 1.  Plasticity of the spinal neural circuitry after injury.

Authors:  V Reggie Edgerton; Niranjala J K Tillakaratne; Allison J Bigbee; Ray D de Leon; Roland R Roy
Journal:  Annu Rev Neurosci       Date:  2004       Impact factor: 12.449

2.  The SCIRehab project: treatment time spent in SCI rehabilitation. Occupational therapy treatment time during inpatient spinal cord injury rehabilitation.

Authors:  Teresa Foy; Ginger Perritt; Deepa Thimmaiah; Lauren Heisler; Jennifer Lookingbill Offutt; Kara Cantoni; Ching-Hui Hseih; Julie Gassaway; Rebecca Ozelie; Deborah Backus
Journal:  J Spinal Cord Med       Date:  2011       Impact factor: 1.985

3.  The SCIRehab project: treatment time spent in SCI rehabilitation. Physical therapy treatment time during inpatient spinal cord injury rehabilitation.

Authors:  Sally Taylor-Schroeder; Jacqueline LaBarbera; Shari McDowell; Jeanne M Zanca; Audrey Natale; Sherry Mumma; Julie Gassaway; Deborah Backus
Journal:  J Spinal Cord Med       Date:  2011       Impact factor: 1.985

Review 4.  Neuroplasticity after spinal cord injury and training: an emerging paradigm shift in rehabilitation and walking recovery.

Authors:  Andrea L Behrman; Mark G Bowden; Preeti M Nair
Journal:  Phys Ther       Date:  2006-10

5.  The reproducibility and convergent validity of the walking index for spinal cord injury (WISCI) in chronic spinal cord injury.

Authors:  Anthony S Burns; Jude J Delparte; Mary Patrick; Ralph J Marino; John F Ditunno
Journal:  Neurorehabil Neural Repair       Date:  2011-02       Impact factor: 3.919

6.  Reliability and validity of grip and pinch strength evaluations.

Authors:  V Mathiowetz; K Weber; G Volland; N Kashman
Journal:  J Hand Surg Am       Date:  1984-03       Impact factor: 2.230

7.  Functional and corticomotor changes in individuals with tetraplegia following unimanual or bimanual massed practice training with somatosensory stimulation: a pilot study.

Authors:  Larisa R Hoffman; Edelle C Field-Fote
Journal:  J Neurol Phys Ther       Date:  2010-12       Impact factor: 3.649

8.  Relationship of occupational therapy inpatient rehabilitation interventions and patient characteristics to outcomes following spinal cord injury: the SCIRehab project.

Authors:  Rebecca Ozelie; Julie Gassaway; Emily Buchman; Deepa Thimmaiah; Lauren Heisler; Kara Cantoni; Teresa Foy; Ching-Hui Jean Hsieh; Randall J Smout; Scott E D Kreider; Gale Whiteneck
Journal:  J Spinal Cord Med       Date:  2012-11       Impact factor: 1.985

9.  Synergistic effects of BDNF and rehabilitative training on recovery after cervical spinal cord injury.

Authors:  N Weishaupt; S Li; A Di Pardo; S Sipione; K Fouad
Journal:  Behav Brain Res       Date:  2012-11-03       Impact factor: 3.332

10.  Functional status and therapeutic intensity during inpatient rehabilitation.

Authors:  A W Heinemann; B Hamilton; J M Linacre; B D Wright; C Granger
Journal:  Am J Phys Med Rehabil       Date:  1995 Jul-Aug       Impact factor: 2.159

View more
  18 in total

1.  Evaluation of the graded redefined assessment of strength, sensibility and prehension (GRASSP) in children with tetraplegia.

Authors:  M J Mulcahey; Christina Calhoun Thielen; Kathryn Dent; Rebecca Sinko; Cristina Sadowsky; Rebecca Martin; Lawrence C Vogel; Loren Davidson; Heather Taylor; Jackie Bultman; John Gaughan
Journal:  Spinal Cord       Date:  2018-03-26       Impact factor: 2.772

2.  The Rehabilitation Treatment Specification System: Implications for Improvements in Research Design, Reporting, Replication, and Synthesis.

Authors:  Jarrad H Van Stan; Marcel P Dijkers; John Whyte; Tessa Hart; Lyn S Turkstra; Jeanne M Zanca; Christine Chen
Journal:  Arch Phys Med Rehabil       Date:  2018-09-27       Impact factor: 3.966

3.  Cardiovascular Stress During Inpatient Spinal Cord Injury Rehabilitation.

Authors:  Dominik Zbogar; Janice J Eng; Jeremy W Noble; William C Miller; Andrei V Krassioukov; Mary C Verrier
Journal:  Arch Phys Med Rehabil       Date:  2017-06-13       Impact factor: 3.966

4.  Traumatic brain injury rehabilitation in Riyadh, Saudi Arabia: Time to rehabilitation admission, length of stay and functional outcome.

Authors:  Hazem Qannam; Husam Mahmoud; W Ben Mortenson
Journal:  Brain Inj       Date:  2017-03-31       Impact factor: 2.311

5.  Dose-Response Outcomes Associated with Different Forms of Locomotor Training in Persons with Chronic Motor-Incomplete Spinal Cord Injury.

Authors:  Evan B Sandler; Kathryn E Roach; Edelle C Field-Fote
Journal:  J Neurotrauma       Date:  2017-01-04       Impact factor: 5.269

6.  Kinematic and Neuromuscular Adaptations in Incomplete Spinal Cord Injury after High- versus Low-Intensity Locomotor Training.

Authors:  Marzieh M Ardestani; Christopher E Henderson; Seyed H Salehi; Gordhan B Mahtani; Brian D Schmit; T George Hornby
Journal:  J Neurotrauma       Date:  2019-02-01       Impact factor: 5.269

7.  Physical activity outside of structured therapy during inpatient spinal cord injury rehabilitation.

Authors:  Dominik Zbogar; Janice J Eng; William C Miller; Andrei V Krassioukov; Mary C Verrier
Journal:  J Neuroeng Rehabil       Date:  2016-11-15       Impact factor: 4.262

8.  Priming for Improved Hand Strength in Persons with Chronic Tetraplegia: A Comparison of Priming-Augmented Functional Task Practice, Priming Alone, and Conventional Exercise Training.

Authors:  Joyce Gomes-Osman; Jacqueline A Tibbett; Brandon P Poe; Edelle C Field-Fote
Journal:  Front Neurol       Date:  2017-01-17       Impact factor: 4.003

9.  Reliability and validity of daily physical activity measures during inpatient spinal cord injury rehabilitation.

Authors:  Dominik Zbogar; Janice J Eng; William C Miller; Andrei V Krassioukov; Mary C Verrier
Journal:  SAGE Open Med       Date:  2016-09-01

10.  A single-subject study of robotic upper limb training in the subacute phase for four persons with cervical spinal cord injury.

Authors:  Linda Sørensen; Grethe Månum
Journal:  Spinal Cord Ser Cases       Date:  2019-03-12
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.