PEDIATRICS Vol. 120 No. 1 July 2007, pp. 49-58 (doi:10.1542/peds.2007-0016)
ARTICLE |
Botulinum Toxin for Spasticity in Children With Cerebral Palsy: A Comprehensive Evaluation
a Department of Rehabilitation Medicine, Children's Hospital and Regional Medical Center, Seattle, Washington
b Departments of Rehabilitation Medicine
c Pediatrics, University of Washington, Seattle, Washington
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ABSTRACT |
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 TOP ABSTRACT METHODSRESULTSDISCUSSIONCONCLUSIONSREFERENCES |
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BACKGROUND. Spasticity is a prevalent disabling clinical symptom for children with cerebral palsy. Treatment of spasticity with botulinum toxin in children with cerebral palsy was first reported in 1993. Botulinum toxin provides a focal, controlled muscle weakness with reduction in spasticity. Interpretation of the literature is difficult because of the paucity of reliable measures of spasticity and challenges with measuring meaningful functional changes in children with disabilities.
OBJECTIVE. This study documents the effects of botulinum toxin A injections into the gastrocnemius muscles in children with spastic diplegia. Outcomes are evaluated across all 5 domains of the National Centers for Medical and Rehabilitation Research domains of medical rehabilitation.
METHODS. A randomized, double-masked, placebo-controlled design was applied to 33 children with spastic diplegia with a mean age of 5.5 and Gross Motor Function Classification System Levels of I through III. Participants received either 12 U/kg botulinum toxin A or placebo saline injections to bilateral gastrocnemius muscles. Outcomes were measured at baseline and 3, 8, 12, and 24 weeks after injection.
RESULTS. Significant decreases in the electromyographic representation of spasticity were documented 3 weeks after botulinum toxin A treatment. A significant decrease in viscoelastic aspects of spasticity was present at 8 weeks, and subsequent increases in dorsiflexion range were documented at 12 weeks for the botulinum toxin A group. Improvement was found in performance goals at 12 weeks and in maximum voluntary torque and gross motor function at 24 weeks for the botulinum toxin A. There were no significant differences between groups in satisfaction with performance goals, energy expenditure, Ashworth scores, or frequency of adverse effects.
CONCLUSIONS. The safety profile of 12 U/kg of botulinum toxin A is excellent. Although physiologic and mechanical effects of treatment with botulinum toxin A were documented with functional improvement at 6 months, family satisfaction with outcomes were no different. Communication is needed to ensure realistic expectations of treatment.
Key Words: cerebral palsy • botulinum toxin
Abbreviations: BTX—botulinum toxin • BTX-A—botulinum toxin type A • CP—cerebral palsy • ROM—range of motion • NCMRR—National Center for Medical Rehabilitation Research • GMFCS—Gross Motor Function Classification System • GMFM—Gross Motor Function Measure • CHRMC—Children's Hospital and Regional Medical Center • SMS—spasticity measurement system • PT—physical therapy • QEK—quantitative electromyographic kinesiology • DTR—deep-tendon reflexes • PROM—passive range of motion • max torque—maximum voluntary torque • ECI—energy cost index • COPM—Canadian Occupational Performance Measure • GAS—Goal Attainment Scaling • MRV—mean rectified voltage
Since the first report on the use of botulinum toxin (BTX) to treat spasticity in children with cerebral palsy (CP) was published in 1993, there have been >100 articles addressing the intervention. The present literature, including several meta-analyses, suggests that BTX provides focal, controlled muscle weakness and, by implication, reduction in spasticity.1–8 The paucity of reliable measures of spasticity and the difficulty in measuring meaningful changes in function in children with disabilities makes interpretation difficult.
CP, a common chronic disabling condition of childhood, occurs in 1.5 of 1000 to 3 of 1000 live births, with a similar prevalence rate into adolescence and adulthood.9 Spasticity is a prevalent disabling clinical symptom seen in persons with CP. Spastic diplegia a very common form of CP, presents with a wide range of ambulatory outcomes, and is most frequently accompanied by ankle joint spasticity. To justify an intervention, there must be a purpose for treating spasticity that is meaningful to patients and their caregivers. Goals of treatment may include simple aims such as reducing pain, increasing range of motion (ROM), preventing secondary medical complications such as contractures or skin breakdown, or better tolerance of splinting and casting. Most patients and their families identify improved active function related to walking as the most important outcome. Not all patients identify the same functional goals nor do they attach the same priorities to those goals.
We comprehensively studied botulinum toxin type A (BTX-A) injections to gastrocnemius muscle in children with CP by using 14 outcome measures distributed among the 5 domains of science relevant to rehabilitation medicine as defined by the National Centers for Medical and Rehabilitation Research (NCMRR) of the National Institutes of Health.10 These domains include pathophysiology, impairment, functional limitation/activity, disability/participation, and societal limitation/contextual factors (see Tables 1 and 2). This approach afforded a 360° view of the intervention from the pathophysiologic to the societal level. For this project, we combined functional limitation with disability.
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We proposed that BTX-A injection into plantar flexor muscles in children with spastic diplegia would produce a reduction of spasticity and a change in function that could be measured across all 5 domains. This project addressed 8 clinical questions: (1) What is the natural history of the weakness associated with change in neuromuscular junction transmission after injection with BTX? (2) Does injection with BTX-A result in clinically relevant reductions in spasticity, measured by changes in torque and stiffness across the ankle joint, when compared with similar untreated patients? (3) What is the magnitude and durability of reduction of spasticity after treatment with BTX-A? (4) Does injection with BTX-A increase mechanical efficiency, as demonstrated by improvement in the Gross Motor Function Measure (GMFM), reduction of energy expenditure, and improvement of gait? (5) What changes in motor function typically occur during the 6 months after injection with BTX-A? (6) Does injection with BTX-A result in a meaningful reduction in disability as described by the pediatric patient and his/her parents? (7) Does injection with BTX-A reduce societal limitation in the context of community and school activities? (8) Are there serious adverse events or complications of injection with BTX-A during the first 6 months after the procedure?
Our primary hypothesis was that injection with BTX-A would reduce spasticity in plantar flexor muscles of children with spastic diplegia for 6 months' duration and that we could reliably measure that reduction in spasticity. We predicted that the pathophysiologic improvements and reductions in spasticity would return to baseline levels at 6 months. We also hypothesized that injections would improve functional ability and societal participation that although temporary, would be significant and meaningful.
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METHODS |
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Thirty-three children were assigned randomly to either an experimental group (injection with 12 U/kg BTX-A) or a comparison group (sham injection of normal saline) by sealed envelope randomization code generated by a study statistician and pharmacist. Double-masked assessments were made at baselines 1 and 2 (7 days apart) and at 3, 8, 12, and 24 weeks postinjection (see Table 1). Injections occurred at baseline number 2 after masked testing was completed. The timing of the first postintervention assessment at 3 weeks after injection was chosen on the basis of previous published reports suggesting that the maximal effect of the neuromuscular blockade was obtained at 21 days.11 The remaining time points were chosen to assess BTX-A effect duration and document its dissipation. At the end of 24 weeks, the randomization code was unmasked and patients in the sham injection group had the opportunity to cross over and have injection with BTX-A.
Study participants underwent conscious sedation with oral midazolam to improve tolerance of injections. Injections were performed solely by the principal investigator using electromyogram guidance at 2 injection sites in each of the medial and lateral heads of the gastrocnemius muscles. A total dosage of 12 U/kg (never exceeding 400 U) was distributed among left and right gastrocnemius muscles. Assessments were performed in the same order on each assessment day following the schedule in Table 1. The active drug in this clinical trial was botulinum toxin type A (Botox; Allergan Pharmaceuticals, Irvine, CA). Each 100 U of BTX-A was diluted with 1 mL of preservative-free 0.9% sodium chloride for injection. The placebo was 0.9% sodium chloride for injection, prepared to the same volume calculated for the active drug. The study drug was prepared by using the aseptic technique on the day of dosing. All doses were mixed within 4 hours of the time of the injection. The Investigational Drug Service at Children's Hospital and Regional Medical Center (CHRMC) performed the randomization and prepared all doses of the study drug.
Participants were randomly assigned into 4 strata on the basis of age (3–7 vs 8–12 years) and whether they were receiving oral baclofen. Preliminary power analysis was based on the primary outcome measures of spasticity and motor function (ie, spasticity measurement system [SMS] and GMFM). On the basis of the then-current estimates of variance of primary outcome measures, with 18 subjects in each group, we predicted the ability to detect a 7.2-point change in total GMFM percent scores with a power of 0.9 at a 2-tailed significance level of .05. The same sample size would yield a 15.3-point change in path length on the SMS with a power of .8 and will provide a 2-tailed significance of .05. On the basis of our previous experience with measurement of GMFM and SMS, preliminary analysis of the statistical power of this study suggested that a minimum of 36 subjects would provide adequate power to be confident of our results. The investigators, study coordinators, physical therapists, and participants were masked to treatment assignment. Only the staff of the Investigational Drug Service was unmasked. The institutional review board at CHRMC granted approval for the study.
Study Participants
The multidisciplinary Spasticity Management Clinic team at CHRMC initially screened all potential participants. Participants were approached for enrollment if they presented with the clinical indications for gastrocnemius BTX-A treatment and fit the inclusion/exclusion criteria. Inclusion criteria were (1) age 3 to 12 years; (2) diagnosis of spastic diplegia, defined as spastic motor impairment with more involvement of lower limbs than upper, fair to good trunk and head control, and little or no bulbar involvement; (3) community or indoor ambulation status12–14; (4) cooperative and tolerant to testing procedures during clinic screening; (5) no fixed musculoskeletal deformities >15° (ie, normal knee extension range of motion: 0°, ankle dorsiflexion: + 15°, (6) stable social environment; (7) ongoing physical therapy (PT) of a minimum of one 60-minute session per week; and (8) pharmacological treatment (baclofen) for spasticity was not a basis for exclusion. Participants were maintained on a stable, fixed dose 1 month before and throughout the 6-month study period. Orthotic type, wearing schedule, PT regimen, and/or the clinical need for serial casting were documented but not controlled during the study period. All participants received direct PT for a minimum of 1 hour per week during the study period. The therapy regimen was left to the discretion of the treating physical therapist.
A total of 106 children were screened between October 1997 and September 2001, of whom 60 were eligible and approached for participation in the trial. Final enrollment was 33 (55% enrollment rate). Informed consent was obtained from all participants and their guardians. Baseline demographics and outcome measures are presented in Table 3. Participants averaged 5.5 years in age (range: 3.1–11.9), and mobility impairments fell into Gross Motor Function Classification System (GMFCS) levels I to III.15,16 There were no significant differences between groups in the baseline measures, except for walking heart rate (P[r] < .003; Table 3). Seventeen participants were randomized to receive BTX-A, and 16 received saline injections. Six children were taking oral baclofen and were equally distributed by treatment group. None of the participants received BTX injections before participation.
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Measurements
NCMRR domains of science were represented by 14 unique outcome measures. See Tables 1 and 4 for specific measures by domain. Primary outcome measures for the domains of impairment and functional limitation/disability were total and elastic path length as a measure of spasticity (SMS), and the GMFM (GMFM-88 and GMFM-66). Secondary outcomes included: quantitative electromyographic kinesiology (QEK) for the pathophysiology domain, Ashworth, deep-tendon reflexes (DTR), clonus, ankle dorsiflexion passive range of motion (PROM), and maximum voluntary torque (max torque) of the gastrocnemius muscle for the impairment domain. The functional limitation/disability domains were also measured by energy cost index (ECI) and the performance portion of the Canadian Occupational Performance Measure (COPM). The satisfaction portion of the COPM and Goal Attainment Scaling (GAS) was administered to assess the societal limitation domain.
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The QEK and SMS were collected by a study engineer and research assistant masked to group assignment in the research motion analysis laboratory at the University of Washington. Masked research physical therapists and nurses collected the remaining outcome measures in the pediatric clinical research center at CHRMC. A masked research nurse conducted a structured adverse event interview at each research visit in person and by telephone for the 8-week visit. Adverse events reported during those interviews were coded for date of onset and resolution, severity level, relationship to CP and/or treatment, effect on treatment, medical treatments administered, and outcome.
SMS
An electromechanical method of eliciting and measuring spasticity was performed by using automated measurement of ankle stiffness in response to passive ankle movements of various frequencies.17,18 The participant was tested in the prone position and on the leg exhibiting the greatest motor impairment (greatest Ashworth score at screening visit) and with adequate ROM to perform the test. The foot was inserted into a foot binding aligned to the ankle joint and positioned at the subject's maximum dorsiflexion. The foot was passively rotated over 5° at frequencies of 3 to 12 Hz via a custom-designed, computer-controlled actuator. Ankle torque and displacement signals were sampled at 2048 Hz via laptop computer (Apple PowerBook, Cupertino, CA) running custom software written in LabVIEW (National Instruments Corp, Austin, TX) with an analog to digital card (National Instruments DAQCard 1200). Torque values were recorded in Newton-meters (N·m) and the path length in Newton-meters per radian. Data were collected over the course of 30 randomly applied 20-second trials (3 trials at each of 10 frequencies). Concomitant surface electromyogram measurements of tibialis anterior and gastrocnemius muscles, using a TE4 electromyograph (TECA Corp, White Plains, NY), provided visualization of the reflex responses and feedback to the examiner to ensure the subject was otherwise relaxed. Inertial and drag torques were computed and deducted from the total, resulting in computation of net passive resistance and spasticity-induced elastic (ie, position-dependent) and viscous (velocity-dependent) ankle stiffness. Variation of ankle stiffness over the range of applied frequencies formed the basis for quantifying spasticity as a total path length and an elastic path length parameter. Larger path length values indicated greater variations in stiffness with frequency that, in turn, reflected an increased reflex mediated or spastic response.19
GMFM
The GMFM was used to assess changes in gross motor skill and mobility.20 The GMFM is a criterion reference tool designed to measure change in gross motor function over time in children with motor impairment, and has been validated for sensitivity to change in children with CP. Only items from the standing and walk/run/jump dimensions were administered. Both the GMFM-88 and GMFM-66 scores were used to take advantage of the improved scaling with the GMFM-66.21 The masked research physical therapists achieved interrater reliability at >80% point-by-point agreement22 and maintained this for the study's duration by scoring of standard videotaped GMFM evaluations every 6 months. The 2 research physical therapists had a minimum of 8 years clinical experience each in the administration, use, and scoring of the GMFM-88.
QEK and Max Torque
The QEK consisted of training the participants to maximally contract the gastrocnemius muscle group and then measuring the electromyograph-generated voltage amplitude and torque responses. The QEK evaluation was obtained in conjunction with the SMS evaluation. To perform this test, the SMS was used in a static (isometric) configuration with the foot positioned in relative plantar-flexion, that is, at the "low" end of the 5° movement range applied for the SMS measurement. The subject was provided with visual feedback of the torque response to encourage the maximal plantar-flexion effort. Data were collected over a 10-second period using the same hardware as described above for the SMS, but sampled at 500 Hz with electromyograph band-pass filtering over a range of 16 to 160 Hz. The peak plantar-flexing torque over the trial period was determined along with surface electromyographic signal parameters by using custom software written in LabVIEW. A running average of the torque over a 1-second window was computed and the electromyographic signal in this averaging window, during which the torque was maximized, was extracted. This represented the electromyographic activity, which occurred at the time of highest mean plantar-flexing torque. The extracted electromyographic signal was rectified and its mean value calculated and reported as the mean rectified voltage (MRV). MRV is a neurophysiologic representation of the total number of motor units available for muscular contraction. The change in MRV is proportional to the magnitude of the neuromuscular blockade. A brief trial period was conducted to train the participants in applying maximum plantar-flexing torque. With the aid of the visual torque feedback, family members and test personnel provided verbal encouragement to the subject to maximize the level of plantar-flexion torque generated. Three QEK determinations were obtained, and the trial exhibiting the highest peak torque response was used because it reflected the most effective attempt.
Physical Examination Measures
Masked research physical therapists collected modified Ashworth scores on the gastrocnemius muscle group,23 PROM, DTRs, and clonus of the ankle in a standardized manner. Interrater reliability of the research physical therapists was established for the Ashworth scale before the study. The research physical therapists had >28 years combined pediatric clinical experience. The principal investigator (Dr Hays) trained the research therapists in the administration and scoring of ankle DTRs and clonus. DTRs were coded from 0 to 4 on an ordinal scale. Clonus was coded by beats palpated.
Energy Cost Index
To evaluate the effect of treatment on energy expenditure, the ECI was measured by the research therapists and nurses.24,25 Participants walked at a self-selected speed along an oblong 20-meter track for 5 minutes. The participant's average heart rate and walking speed were recorded. ECI was calculated as the average number of heart beats per unit distance walked.
COPM and GAS
Using a semistructured interview recommended by the COPM guidelines, 3 performance outcomes (goals) were identified at baseline by the parent and child with the research physical therapist.26,27 These included such goals as "decrease in falling on the playground at school or climb stairs without physical help." Serial measurements of the COPM performance and satisfaction scores were ranked by importance and then measured by report from the parent. The same 3 performance outcomes (goals) were then structured for goal attainment scaling in the GAS through semistructured interview and by collaboration between the research physical therapist, parent, and child.28,29 The formula derived by Kiresuk and Sherman30 was used to calculate standardized scores (t score), reflecting the composite change for the 3 a priori goals over the 6-month study period.
Adverse Events
Structured adverse event interviews were administered in person by the research nurse at all visits except the 8-week visit, which was done by telephone. All events reported during those interviews were coded for severity and relationship to CP and BTX-A or saline injection.
Analysis
The data were entered into the SPSS for Windows 10.05 (SPSS Inc, Chicago, IL) software format for analysis. Change scores were calculated from the average of the 2 baseline assessments to each follow-up assessments time point for the primary outcomes (Table 1). At each follow-up time point, the differences in change scores were compared between the BTX-A and placebo groups with the Wilcoxon Mann-Whitney U nonparametric test for the primary outcome variables. Secondary outcome measures of Ashworth scale, clonus, and DTR change scores at each follow-up time point were also assessed by the same nonparametric statistic because of the lack of a normal distribution. Change score from baseline to each follow-up time point for QEK MRV, max torque, COPM performance, and satisfaction, GAS, and ROM were compared between treatment groups by an unpaired t test. The frequency of adverse events by group was analyzed by 
2. Baseline walking heart rate was found to be significantly different between treatment groups (Table 3) and was corrected for in the regression analysis of ECI change from baseline. Change-score statistics (mean, SD or median, range) for the appropriate tests for each outcome measure are displayed in Table 4.
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RESULTS |
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Pathophysiology
The known neurophysiologic effect of BTX injections compared with placebo was confirmed at 3 weeks' postinjection by a significant decrease in QEK (MRV-µV, P < .05). This neurophysiological difference was no longer present by 8 weeks. By 24 weeks, the BTX group QEK had surpassed the placebo group, although not significantly (Fig 1 and Table 4).
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Impairment
Significant decreases in SMS total (P < .04) and elastic path length (P < .05) changes from baseline were documented at 8 weeks' postinjection for the BTX group compared with the placebo group. A change in path length for the BTX group compared with the placebo from baseline was present at 12 weeks but did not reach significance (see Figs 2 and 3 and Table 4). No significant differences in change scores by group were found for Ashworth change scores at any follow-up time point (see Table 4). The changes in the clinical measures of Achilles DTR and clonus were significantly decreased in the BTX group at 3 weeks only (Table 4). Ankle dorsiflexion PROM with the knee extended significantly increased for the BTX group (P < .05) compared with the placebo group at 12 weeks with a mean difference of 4.2 degrees (Fig 4 and Table 4). QEK maximum torque changes from baseline were significantly greater for the BTX group at 24 weeks postinjection (P < .03) (Fig 5 and Table 4).
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Functional Activity/Disability
GMFM-88 total scores approached a significant difference at 3 weeks, with the BTX group scoring higher. Both groups improved their change from baseline scores over the study period with a significant median difference documented at 24 weeks (P < .001; Fig 6 and Table 4). GMFM-66 change from baseline scores for the BTX group was also significantly greater than the placebo group at 24 weeks (3.1 BTX vs 1.2 control, P < .03; Fig 7 and Table 4). No significant differences between treatment group change scores were found at any follow-up time point for ECI (Table 4). COPM performance change scores from baseline were significantly greater for the BTX group at 12 weeks (1.7 BTX vs 1.2 placebo; P < .04). At 24 weeks, the BTX group continued with higher change scores than the placebo group but did not reach significance (Fig 8 and Table 4). The significant changes from baseline documented for individuals in the BTX group suggest improved gait and related upright motor skills (ie, stair climbing, 1-leg balance, jumping).
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Societal Participation
The COPM satisfaction change scores and GAS t scores increased from baseline to 12- and 24-week follow-up for both groups. No significant differences in change scores between groups were found at 12 or 24 weeks' follow-up (P > .12–.98) in Figs 9 and 10 and Table 4.
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Adverse Events
A total of 56 adverse events potentially having any relationship to treatment (injection of BTX-A or saline) were reported during the 6-month study period for both treatment groups. The frequency of adverse events by treatment group (30 for BTX, 26 for placebo) was not significantly different between the groups (P = .22). Six of these events required ibuprofen for muscle soreness at injection site (3 per treatment group), and 3 decreased their activity level for 24 hours after injection.
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DISCUSSION |
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TOPABSTRACTMETHODSRESULTSDISCUSSIONCONCLUSIONSREFERENCES |
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This is the first randomized, controlled trial of BTX treatment to report outcomes globally across all domains of the NCMRR framework. We have attempted to address a question that has been characterized by Sheean31 as the "holy grail" of BTX investigation, which is to document not only physiologic effect but functional benefit. We have also attempted to avoid the 4 most common barriers to good clinical research regarding BTX. These include inappropriate outcome measures, inappropriate patient selection, inappropriate injection protocols, and poor general study design.31
We were gratified that our physiologic measure of motor strength reduction after treatment with BTX-A, the MRV measure of the QEK, differed significantly from the placebo group and mirrored the descriptions of BTX effect described in experimental animal studies. This finding, a significant reduction at 3 weeks, indicated that the neuromuscular junction transmission was genuinely altered and that the injection technique was valid and reliable.
Significant reduction in spasticity was documented. The most robust evidence was found in the change in mean total and elastic path lengths measured at 8 weeks by using the SMS. This finding was supported by significant changes in the DTRs and clonus at the ankle joint. The increases in dorsiflexion ROM at 12 weeks may have been related to the changes in the viscoelastic properties of the muscle that followed the initial neuromuscular blockade and were maintained through more effective active use of the muscle in gait. Significant changes in the voluntary torque documented at 24 weeks may most likely be a direct response to the improved ROM. This apparent chain of improvements in different aspects of function is consistent with real physiologic change.
GMFM and gastrocnemius torque results show significant consistent changes in mechanical efficiency and motor function at 6 months after treatment. This was surprising and may represent the time required to adjust to the changes in motor strength, ROM, and the reduction of interfering spasticity. The later changes in motor function and strength support an argument for consistent therapy to maintain and maximize the effects of BTX-A treatment, to facilitate acquisition of new skills or improved efficiency, and a longer period before reinjection with BTX. No significant change in energy expenditure using the ECI was found.
We measured a significant change in the experimental subjects' performance with the COPM after treatment compared with the placebo group, but we were unable to demonstrate a meaningful difference in either the satisfaction scores of the COPM or the mean change in t scores via GAS. This result was intriguing.
The results of this project both parallel and contrast with other randomized, control trials of BTX in ambulatory youth with CP. Sutherland and colleagues32 documented improved ankle dorsiflexion and swing during walking with 3 dimensional gait analysis at 3 months' post-BTX injections. The improvement in GMFM-88 total and GMFM-66 scores found in this project at 6 months reflects global changes in walking skill and are in line with the gait analysis outcomes found by Sutherland. Using a clinical observational scale to quantify parameters of gait, Koman et al33 also documented improved gait patterns at 12 weeks' postinjection with BTX in a mixed sample of youth with hemiplegia and diplegia CP. Komen and colleagues33 also noted significant improvements in ankle range of motion which is consistent with data we report here in Table 4. In 2000, Ubhi and colleagues34 reported significant improvements in GMFM walking skills at 3 months after BTX injections for ankle equinus in a group of children with hemiplegia (30%) and diplegia motor involvement. We did not find this improvement in gross motor skills in our study sample until 6 months after injection. The lack of significant improvement in the physiologic cost index reported by Ubhi and coauthors is consistent with our findings for ECI. Their results contrast with the changes documented in ankle ROM (Table 4). These conflicting results may be a function of mixed study samples containing both youth with hemiplegia and diplegia as well as older children studied. None of these studies looked at outcomes at 6 months after injection.
Reddihough et al35 followed subjects for 6 months and documented no significant improvement in GMFM scores at 3 and 6 months after BTX injections in children with spastic diplegic CP. The age of their study population was similar to subjects in our project, but >60% of their study sample were GMFCS levels III and IV, suggesting they were treating subjects with lower walking skills levels than the subjects in our study sample where 50% were GMFCS level II. Most recently, Scholtes and colleagues36 in the Netherlands also reported improved GMFM scores that were similar to our results at 6 months. They used multilevel BTX-A injections and provided comprehensive rehabilitation in 46 children across GMFCS levels I-IV.
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CONCLUSIONS |
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TOPABSTRACTMETHODSRESULTSDISCUSSIONCONCLUSIONSREFERENCES |
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It seems that the physiologic and mechanical effects of treatment with BTX-A are genuine and measurable in youth with spastic diplegia CP. However, these effects may not create enough change in the patients' function or the families' perception of function to register as a meaningful improvement in their societal participation. It is possible that these changes were too subtle to be recognized with conventional satisfaction measures. The failure to demonstrate a match between the measured effect and the perceived benefit of treatment is perhaps 1 of the most important findings of our study. Detailed information describing expected functional improvements after treatment, based on studies such as this one, must be communicated to families in useful, understandable terms to ensure that they enter into treatment with truly informed consent. Our study suggests that patients and families must have realistic expectations about BTX treatment before they enter into it or risk experiencing measurable effect without perceived benefit.
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ACKNOWLEDGMENTS |
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Funding for this project was through the NCMRR, National Institutes of Health grant RO1 HD35750, and grant M01-RR-00037 of the University of Washington General Clinic Research Center from the National Center for Research Resources, National Institutes of Health. The BTX-A was supplied by Allergan Pharmaceuticals, Irvine, CA.
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FOOTNOTES |
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Accepted Mar 2, 2007.
Address correspondence to Kristie Bjornson, PhD, PT, Children's Hospital and Regional Medical Center, MPW 8-3, 4800 Sand Point Way NE, Seattle, WA 98105. E-mail: kristie.bjornson{at}seattlechildrens.org
The authors have indicated they have no financial interests relevant to this article to disclose.
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