Tag Archives: Scoliosis Surgery
Cerebral palsy: the whys and hows – Cerebral Palsy Research
1. Arch Dis Child Educ Pract Ed. 2012 Aug;97(4):122-31.
Cerebral palsy: the whys and hows.
Fairhurst C.
Correspondence to Dr Charlie Fairhurst, Department of Paediatric Neurodisability, Evelina Children’s Hospital,
Guy’s and Saint Thomas’ Foundation NHS trust, London SE1 9RT, UK; charlie.fairhurst@gstt.nhs.uk.
The descriptive term of cerebral palsy encompasses the largest group of childhood movement disorders. Severity
and pattern of clinical involvement varies widely dependent on the area of the central nervous system
compromised. A multidisciplinary team approach is vital for all the aspects of management to improve function and
minimise disability. From a medical viewpoint, there are two pronged approaches. First a focus on developmental
and clinical comorbidities such as communication, behaviour, epilepsy, feeding problems, gastro-oesophageal
reflux and infections; and second on specifics of muscle tone, motor control and posture. With regards to the latter,
there is an increasing number of available treatments including oral antispasticity and antidystonic medications,
injectable botulinum toxin, multilevel orthopaedic and neurosurgical options and a variety of complementary and
alternative therapies.
PMID: 22868578 [PubMed - in process]
2. Assist Technol. 2012 Summer;24(2):78-86.
Wheelchair components and pulmonary function in children with cerebral palsy.
Barks L, Davenport P.
VA HSR&D/RR&D Research Center of Excellence, Tampa, FL 33544, USA. Lelia.Barks@va.gov
OBJECTIVE: This study investigates the effects of four individual wheelchair components (upper extremity
supports, lateral trunk supports, anterior pelvic belt, and 30 degree posterior seat tilt), on pulmonary function in
prepubertal children with cerebral palsy (CP). METHODS: Participants who range in age from 5-10 years were
evaluated using four wheelchair components in six configurations (conditions 1-6) using a planar seating simulator.
The Respironics Non Invasive Cardiac Output monitor (NICO) and MasterScreen Impulse Oscillometry System
(IOS) measured pulmonary function parameters. Repeated measures ANOVA was used to analyze effect of
Monday 13 August 2012
Cerebral Palsy Alliance
PO Box 184 Brookvale NSW 2100 Australia | T +61 2 9479 7200 | www.cerebralpalsy.org.au
Interventions and Management
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Professor Nadia Badawi
Macquarie Group Foundation Chair of Cerebral Palsy
PO Box 560, Darlinghurst, New South Wales 2010 Australia
Cerebral Palsy Alliance
PO Box 184 Brookvale NSW 2100 Australia | T +61 2 9479 7200 | www.cerebralpalsy.org.au 2
wheelchair conditions on total airway resistance (R(AW)). RESULTS: Eight participants completed the protocol. R
(AW) and minute ventilation (MV) varied with wheelchair condition. Lowest R(AW) was seen with two upper
extremity supports or two lateral trunk supports. Differences were not significant (p = 0.253). CONCLUSIONS: The
NICO and IOS, independent of participant effort, measured R(AW) and MV, which varied by wheelchair seating
condition. More research is needed with a larger sample to determine seating components’ impact on pulmonary
function. These methods objectively measured pulmonary function of young children with CP in wheelchairs and
could facilitate further research into benefits of wheelchair postural support components.
PMID: 22876730 [PubMed - in process]
3. BMC Pediatr. 2012 Aug 9;12(1):120. [Epub ahead of print]
Evaluation of the effects of Botulinum toxin A injections when used to improve ease of care and comfort in
children with cerebral palsy whom are non-ambulant: a double blind randomized controlled trial.
Thorley M, Donaghey S, Edwards P, Copeland L, Kentish M, McLennan K, Lindsley J, Gascoigne-Pees L,
Sakzewski L, Boyd
BACKGROUND: Children with cerebral palsy (CP) whom are non-ambulant are at risk of reduced quality of life and
poor health status. Severe spasticity leads to discomfort and pain. Carer burden for families is significant. This
study aims to determine whether intramuscular injections of Botulinum Toxin A (BoNT-A) combined with a regime of
standard therapy has a positive effect on care and comfort for children with CP whom are non-ambulant (GMFCS
IV/V), compared with standard therapy alone (cycle I), and whether repeated injections with the same regime of
adjunctive therapy results in greater benefits compared with a single injecting episode (cycle II). The regime of
therapy will include serial casting, splinting and/or provision of orthoses, as indicated, combined with four sessions
of goal directed occupational therapy or physiotherapy. Method/design This study is a double blind randomized
controlled trial. Forty participants will be recruited. In cycle I, participants will be randomized to either a treatment
group who will receive BoNT-A injections into selected upper and/or lower limb muscles, or a control group who will
undergo sham injections. Both groups will receive occupational therapy and /or physiotherapy following injections.
Groups will be assessed at baseline then compared at 4 and 16 weeks following injections or sham control.
Parents, treating clinicians and assessors will be masked to group allocation. In cycle II, all participants will undergo
intramuscular BoNT-A injections to selected upper and/or lower limb muscles, followed by therapy. The primary
outcome measure will be change in parent ratings in identified areas of concern for their child’s care and comfort,
using the Canadian Occupational Performance Measure (COPM). Secondary measures will include the Care and
Comfort Hypertonicity Scale (ease of care), the Cerebral Palsy Quality of Life Questionnaire (CP QoL-Child) (quality
of life), the Caregiver Priorities and Child Health Index of Life with Disabilities Questionnaire (CPCHILD(c)) (health
status) and the Paediatric Pain Profile (PPP) (pain). Adverse events will be carefully monitored by a clinician
masked to group allocation. DISCUSSION: This paper outlines the theoretical basis, study hypotheses and
outcome measures for a trial of BoNT-A injections and therapy for children with non-ambulant cerebral palsy. Trial
registration Australia New Zealand Clinical Trials Registry:N12609000360213.
PMID: 22873758 [PubMed - as supplied by publisher]
4. Gait Posture. 2012 Aug 4. [Epub ahead of print]
Differences in implementation of gait analysis recommendations based on affiliation with a gait laboratory.
Wren TA, Elihu KJ, Mansour S, Rethlefsen SA, Ryan DD, Smith ML, Kay RM.
Children’s Orthopaedic Center, Children’s Hospital Los Angeles, Los Angeles, CA, United States; Keck School of
Medicine, University of Southern California, Los Angeles, CA, United States.
This study examined the extent to which gait analysis recommendations are followed by orthopedic surgeons with
varying degrees of affiliation with the gait laboratory. Surgical data were retrospectively examined for 95 patients
with cerebral palsy who underwent lower extremity orthopedic surgery following gait analysis. Thirty-three patients
were referred by two surgeons directly affiliated with the gait laboratory (direct affiliation), 44 were referred by five
surgeons from the same institution but not directly affiliated with the gait laboratory (institutional affiliation), and 18
were referred by 10 surgeons from other institutions (no affiliation). Data on specific surgeries were collected from
Cerebral Palsy Research News ~ Monday 13 August 2012
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the gait analysis referral, gait analysis report, and operative notes. Adherence to the gait analysis recommendations
was calculated by dividing the number of procedures where the surgery followed the gait analysis recommendation
(numerator) by the total number of procedures initially planned, recommended by gait analysis, or done
(denominator). Adherence with the gait analysis recommendations was 97%, 94%, and 77% for the direct,
institutional, and no affiliation groups, respectively. Procedures recommended for additions to the surgical plan
were added 98%, 87%, and 77% of the time. Procedures recommended for elimination were dropped 100%, 89%,
and 88% of the time. Of 81 patients who had specific surgical plans prior to gait analysis, changes were
implemented in 84% (68/81) following gait analysis recommendations. Gait analysis influences the treatment
decisions of surgeons regardless of affiliation with the gait laboratory, although the influence is stronger for
surgeons who practice within the same institution as the gait laboratory.
Copyright © 2012 Elsevier B.V. All rights reserved.
PMID: 22871237 [PubMed - as supplied by publisher]
5. Hip Int. 2012 Aug 7:0. doi: 10.5301/HIP.2012.9453. [Epub ahead of print]
Hip flexion deformity improves without psoas-lengthening after surgical correction of fixed knee flexion
deformity in spastic diplegia.
Rutz E, Gaston MS, Tirosh O, Brunner R.
Paediatric Orthopaedic Department, University Children’s Hospital Basle, Basle – Switzerland; and Murdoch
Children’s Research Institute, The Royal Children’s Hospital, Victoria – Australia.
Background: It is unclear if psoas lengthening surgery is required in the treatment of patients with cerebral palsy
(CP) with hip flexion deformity and previous studies show equivocal results with regard to functional outcome.
Methods: This study retrospectively assessed 12 patients with a diagnosis of spastic diplegia who underwent single
event multilevel surgery in order to correct deformities in the sagittal plane distal to the hip. Both clinical and
instrument gait analysis results were recorded preoperatively, at one year (short term) and at five years (mid term)
postoperatively. Results: Clinically measured hip and knee movement improved at both short and mid term follow
up. Correlations of clinically measured maximum hip and knee extension were significant at all three time points.
Angles at terminal stance/toe off for hip and knee from kinematic data also showed significant correlations at all
three time points. Conclusions: Our study demonstrates that the hip flexion deformities encountered in these
patients will improve spontaneously when the distal fixed knee flexion deformity is surgically corrected. Therefore
correction at the knee allows the ground reaction force to assume a more normal position resulting in correction at
the hip over time. This then removes the need for surgery at the hip level. This fact is especially important when
applied to psoas lengthening as this procedure can cause significant reduction in propulsion power.
PMID: 22878968 [PubMed - as supplied by publisher]
6. J Biomech. 2012 Aug 3. [Epub ahead of print]
Medial gastrocnemius muscle fascicle active torque-length and Achilles tendon properties in young adults
with spastic cerebral palsy.
Barber L, Barrett R, Lichtwark G.
School of Physiotherapy and Exercise Science & Centre for Musculoskeletal Research, Griffith University, Gold
Coast campus, Queensland 4222, Australia.
Individuals with spastic cerebral palsy (CP) typically experience muscle weakness. The mechanisms responsible
for muscle weakness in spastic CP are complex and may be influenced by the intrinsic mechanical properties of the
muscle and tendon. The purpose of this study was to investigate the medial gastrocnemius (MG) muscle fascicle
active torque-length and Achilles tendon properties in young adults with spastic CP. Nine relatively high functioning
young adults with spastic CP (GMFCS I, 17±2 years) and 10 typically developing individuals (18±2 years)
participated in the study. Active MG torque-length and Achilles tendon properties were assessed under controlled
conditions on a dynamometer. EMG was recorded from leg muscles and ultrasound was used to measure MG
Cerebral Palsy Research News ~ Monday 13 August 2012
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PO Box 184 Brookvale NSW 2100 Australia | T +61 2 9479 7200 | www.cerebralpalsy.org.au 4
fascicle length and Achilles tendon length during maximal isometric contractions at five ankle angles throughout the
available range of motion and during passive rotations imposed by the dynamometer. Compared to the typically
developing group, the spastic CP group had 33% lower active ankle plantarflexion torque across the available
range of ankle joint motion, partially explained by 37% smaller MG muscle and 4% greater antagonistic cocontraction.
The Achilles tendon slack length was also 10% longer in the spastic CP group. This study confirms
young adults with mild spastic CP have altered muscle-tendon mechanical properties. The adaptation of a longer
Achilles tendon may facilitate a greater storage and recovery of elastic energy and partially compensate for
decreased force and work production by the small muscles of the triceps surae during activities such as locomotion.
Copyright © 2012 Elsevier Ltd. All rights reserved.
PMID: 22867763 [PubMed - as supplied by publisher]
7. J Neurol. 2012 Aug 10. [Epub ahead of print]
Botulinum toxin therapy: its use for neurological disorders of the autonomic nervous system.
Dressler D.
Movement Disorders Section, Department of Neurology, Hannover Medical School, Carl-Neuberg-Str. 1, 30625,
Hannover, Germany, dressler.dirk@mh-hannover.de.
Botulinum toxin (BoNT) has gained widespread use for the treatment of overactive muscles, overactive exocrine
glands and, most recently, non-muscular pain conditions. Autonomic conditions treated with BoNT include
achalasia, gastroparesis, sphincter of Oddi spasms, and unspecific esophageal spasms in gastroenterology and
prostate disorders in urology. BoNT’s use for autonomic conditions related to neurology includes various forms of
bladder dysfunction (detrusor sphincter dyssynergia, idiopathic detrusor overactivity, neurogenic detrusor
overactivity, urinary retention and bladder pain syndrome), pelvic floor disorders (pelvic floor spasms and anal
fissures), hyperhidrosis (axillary, palmar, and plantar hyperhidrosis, diffuse sweating, Frey’s syndrome) and
hypersalivation (hypersalivation in Parkinsonian syndromes, motor neuron disease, neuroleptic use, and cerebral
palsy). Hyperhidrosis, hypersalivation, some forms of bladder dysfunction and pelvic floor disorders can easily be
treated by neurologists. Most bladder dysfunctions require cooperation with urology departments.
PMID: 22878428 [PubMed - as supplied by publisher]
8. Spine (Phila Pa 1976). 2012 Aug 3. [Epub ahead of print]
Mortality and Morbidity in Early Onset Scoliosis Surgery.
Phillips JH, Knapp DR Jr, Herrera-Soto J.
Orlando Health-Arnold Palmer Medical Center, Pediatric Orthopaedics, 83 W. Columbia Street, Orlando, Florida
32806, Tel: 321.841.3060, Fax: 321.843.6304, Email: jonathan.phillips@orlandohealth.com Orlando Health-Arnold
Palmer Medical Center, Pediatric Orthopaedics, 83 W. Columbia Street, Orlando, Florida 32806, Tel: 321.841.3060,
Fax: 321.843.6304, Email: raymond.knapp@orlandohealth.com Orlando Health-Arnold Palmer Medical Center,
Pediatric Orthopaedics, 83 W. Columbia Street, Orlando, Florida 32806, Tel: 321.841.3060, Fax: 321.843.6304,
Email: jose.herrera@orlandohealth.com.
STRUCTURED: Study Design. Retrospective chart review. Objective. To accurately determine complication rates,
particularly mortality rates, in surgically treated Early Onset Scoliosis. Summary of Background Data. The advent of
modern segmental instrumentation for spinal fusion surgery in adolescent scoliosis has allowed for application of
similar non-segmental un-fused techniques aimed at controlling scoliosis in the very young child. The dismal
prognosis for these children without repeated spinal lengthening procedures is unquestioned though no controlled
trials exist. Many if not most of these children need surgery, however the surgical complication rate is very high.
Methods. During the study period all surgically treated children with EOS seen at our institution were identified.
Inclusion criteria were: any patient who presented to our clinic with early onset scoliosis which was surgically
managed. The total number of procedures, type of implants, number and type of complications, geographic origin of
the cases and final outcomes were all assessed. Results. A total of 165 surgical procedures on 28 patients accrued
Cerebral Palsy Research News ~ Monday 13 August 2012
Cerebral Palsy Alliance
PO Box 184 Brookvale NSW 2100 Australia | T +61 2 9479 7200 | www.cerebralpalsy.org.au 5
over the study time period, including index implantation of instrumentation, lengthening and definitive fusion as well
as operations performed for complications such as wound debridement and revision of failed implants. Clinical
diagnoses included congenital scoliosis, syndromic and chromosomal abnormalities, cerebral palsy and spinal
muscular atrophy. There was a complication rate of 84% overall with a mortality rate of almost 18%. The only
patients with no complications were those whose entire surgical course had been at our institution only. The
mortality rate was equal in patients whose treatment was performed elsewhere versus exclusively in our center.
Conclusion. This study underlines the grave severity of these scolioses particularly in syndromic children. The high
mortality rate is alarming, suggesting that further study is needed in this area.
PMID: 22869061 [PubMed - as supplied by publisher]
9. Clin Linguist Phon. 2012 Sep;26(9):806-22.
Relationship between kinematics, F2 slope and speech intelligibility in dysarthria due to cerebral palsy.
Rong P, Loucks T, Kim H, Hasegawa-Johnson M.
Department of Speech and Hearing Science , University of Illinois , Champaign, IL , USA.
A multimodal approach combining acoustics, intelligibility ratings, articulography and surface electromyography was
used to examine the characteristics of dysarthria due to cerebral palsy (CP). CV syllables were studied by obtaining
the slope of F2 transition during the diphthong, tongue-jaw kinematics during the release of the onset consonant,
and the related submental muscle activities and relating these measures to speech intelligibility. The results show
that larger reductions of F2 slope are correlated with lower intelligibility in CP-related dysarthria. Among the three
speakers with CP, the speaker with the lowest F2 slope and intelligibility showed smallest tongue release
movement and largest jaw opening movement. The other two speakers with CP were comparable in the amplitude
and velocity of tongue movements, but one speaker had abnormally prolonged jaw movement. The tongue-jaw
coordination pattern found in the speakers with CP could be either compensatory or subject to an incompletely
developed oromotor control system.
PMID: 22876770 [PubMed - in process]
10. Oral Surg Oral Med Oral Pathol Oral Radiol. 2012 Sep;114(3):e10-4. Epub 2012 Feb 28.
Oral myiasis: does an indication for surgical treatment still exist? Two case reports.
Ribeiro AL, de Almeida TE, Júnior JS, de Araújo Castro JF, de Jesus Viana Pinheiro J.
Professor, Department of Oral and Maxillofacial Surgery, School of Dentistry, University Center of Pará-CESUPA,
Belém, Brazil; Chairman, Department of Oral and Maxillofacial Surgery, Hospital Metropolitano de Urgência e
Emergência, Belém, Brazil.
OBJECTIVE: Oral myiasis is a rare infection for which treatment protocol has not yet been established. This article
presents 2 cases treated with a combination of topical application of sulfuric ether and surgery. The reasons for the
use of surgical therapy, as well as the possible advantages and disadvantages of drug-based treatments, are
discussed. CASE REPORT: Two cases of oral myiasis are described, the first being observed in a 9-year-old child
with hypotonic cerebral palsy, and the second in a 52-year-old adult, alcohol-dependant, both showing infection in
the gingival sulcus. Both cases were successfully treated in a process that involved topical application of sulfuric
ether, mechanical removal of larvae, and surgical debridement. CONCLUSIONS: Oral myiasis can be treated
effectively with surgery after topical application of sulfuric ether. The use of drugs may suggest a therapeutic
alternative, but still requires further study and experience to be implemented, especially in individuals with
neurological disorders.
Copyright © 2012 Elsevier Inc. All rights reserved.
PMID: 22862986 [PubMed - in process]
Cerebral Palsy Research News ~ Monday 13 August 2012
Cerebral Palsy Alliance
PO Box 184 Brookvale NSW 2100 Australia | T +61 2 9479 7200 | www.cerebralpalsy.org.au 6
11. Int J Rehabil Res. 2012 Aug 3. [Epub ahead of print]
Comparison between utility of the Thai Pediatric Quality of Life Inventory 4.0 Generic Core Scales and 3.0
Cerebral Palsy Module.
Tantilipikorn P, Watter P, Prasertsukdee S.
Division of Physiotherapy, School of Health and Rehabilitation Science, The University of Queensland, St Lucia,
Queensland, Australia bFaculty of Physical Therapy, Mahidol University, Salaya, Nakornprathom, Thailand.
Health-related quality of life (HRQOL) is increasingly being considered in the management of patients with various
conditions. HRQOL instruments can be broadly classified as generic or disease-specific measures. Several generic
HRQOL instruments in different languages have been developed for paediatric populations including the Pediatric
Quality of Life Inventory 4.0 (PedsQL 4.0) Generic Core Scale. This tool and a condition-specific tool, PedsQL 3.0
Cerebral Palsy (CP) Module, are widely used in children with CP. No psychometric properties have been reported
for Thai PedsQL 4.0. Therefore, this study aimed to explore the psychometric properties of the Thai version of the
PedsQL 4.0 Generic Core Scales and compare these with the values for the Thai PedsQL 3.0 CP Module reported
previously. Thai PedsQL 4.0 Generic Core Scales and the PedsQL 3.0 CP Module were completed, respectively,
by children with CP and their parents or caregivers twice within 2-4 weeks. Respondents were 97 parents or
caregivers and 54 children. Minimal missing data were found in most scales. Acceptable internal consistency was
supported, except for Emotional, Social, and School Functioning. Intraclass correlation coefficients for parent-proxy
report and self-report were good to excellent (0.625-0.849). The feasibility and reliability of the Thai PedsQL 4.0
Generic Core Scales were supported. The Thai PedsQL 3.0 CP Module showed higher values for the psychometric
properties. Low-to-good correlations were found among the scales between the PedsQL 4.0 Generic Core Scales
and the 3.0 CP Module. Both instruments could be used to measure HRQOL for children with CP, and may provide
different information.
PMID: 22868944 [PubMed - as supplied by publisher]
12. Soc Work Health Care. 2012;51(4):279-95.
Social workers as transition brokers: facilitating the transition from pediatric to adult medical care.
Shanske S, Arnold J, Carvalho M, Rein J.
Department of Social Work, Children’s Hospital Boston, Boston, Massachusetts 02115, USA.
susan.shanske@childrens.harvard.edu
Transition from pediatric to adult medical care and the significant psychosocial considerations impacting this
developmental process are a primary focus in health care today. Social workers are often the informal brokers of
this complex and nuanced process and are uniquely trained to complete biopsychosocial assessments to
understand the needs of patients and families and address psychosocial factors. Their extensive knowledge of
resources and systems, along with their sophisticated understanding of the relationship issues, family dynamics,
cultural implications, and basic person-in-context approach allow for unique collaboration with the health care team,
family, and community supports to develop successful transition plans and programs.
PMID: 22489554 [PubMed - indexed for MEDLINE]
Cerebral Palsy Research News ~ Monday 13 August 2012
13. Genet Couns. 2012;23(2):215-21.
Pure distal 9p deletion in a female infant with cerebral palsy.
Chen CP, Lin SP, Su YN, Su JW, Chern SR, Town DD, Wang W.
Department of Obstetrics and Gynecology, Mackay Memorial Hospital, Taipei, Taiwan. cpc_mmh@yahoo.com
We report cytogenetic and molecular characterization of a 15.63-Mb pure distal deletion of chromosome 9p (9p22.3
–>pter) in a l 1/2-year-old female infant with cerebral palsy and diffuse cerebral dysfunction. The deletion is of
paternal origin and encompasses the genes of ANKRDS15, DOCK8, FOXD4 and VLDLR. We discuss the genotype
-phenotype correlation in this case with neurological dysfunction and a distal 9p deletion of paternal origin.
PMID: 22876580 [PubMed - in process]
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