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Cerebral palsy

Discussion in 'Pediatrics' started by Admin2, Jan 13, 2006.

  1. NewsBot

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    Articles:
    1
    Crouch gait or flexed-knee gait in cerebral palsy: Is there a difference? A systematic review
    R.O’SullivanA.MarronK.Brady
    Gait & Posture ;Volume 82, October 2020, Pages 153-160
     
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    Articles:
    1
    Foot and ankle somatosensory deficits in children with cerebral palsy: A pilot study
    Anastasia Zarkou et al
    J Pediatr Rehabil Med. 2021 Apr 23
     
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    Articles:
    1
    Is the Prevalence of Equinus Foot in Cerebral Palsy Overestimated? Results from a Meta-Analysis of 4814 Feet
    Axel Horsch et al
    J Clin Med. 2021 Sep 13;10(18):4128
     
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    Articles:
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    Long-term Outcomes of Talonavicular Arthrodesis for the Treatment of Planovalgus Foot in Children With Cerebral Palsy
    Ana Ramírez-Barragán, María Galán-Olleros, Raquel Maroto, Rosa M Egea-Gámez, Ignacio Martínez-Caballero
    J Pediatr Orthop. 2022 Feb 8
     
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    Articles:
    1
    Ankle Dorsiflexor Function after Gastrocsoleus Lengthening in Children with Cerebral Palsy: A Literature Review
    Nicholas Sclavos et al
    Medicina (Kaunas). 2022 Mar 2;58(3):375
     
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    Articles:
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    Gait Analysis in Children with Cerebral Palsy: Are Plantar Pressure Insoles a Reliable Tool?
    Maria Raquel Raposo et al
    Sensors (Basel). 2022 Jul 13;22(14):5234
     
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    Articles:
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    Defining Equinus Foot in Cerebral Palsy
    Axel Horsch et al
    Children (Basel). 2022 Jun 25;9(7):956
     
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    Articles:
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    Long-term outcome of extraarticular subtalar arthrodesis in children with cerebral palsy using modified Grice technique
    Jiri Jochymek, Tereza Peterkova
    Acta Orthop Belg. 2022 Jun;88(2):223-230
     
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    Articles:
    1
    Analysis of Running Gait in Children with Cerebral Palsy: Barefoot vs. a New Ankle Foot Orthosis
    Federica Camuncoli et al
    Int J Environ Res Public Health. 2022 Oct 30;19(21):14203
     
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    Articles:
    1
    Assessment of Five-Foot Plantar Morphological Pressure Points of Children with Cerebral Palsy Using or Not Dynamic Ankle Foot Orthosis
    Senem Guner et al
    Children (Basel). 2023 Apr 13;10(4):722
     
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    Articles:
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    Parent experience with ankle-foot orthoses for their young children with cerebral palsy: a qualitative study
    Pegah Firouzeh et al
    Disabil Rehabil. 2023 Jun 3;1-8
     
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    Articles:
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    Ankle-foot orthoses among children with cerebral palsy: a cross-sectional population-based register study of 8,928 children living in Northern Europe
    Jessica Stockman et al
    BMC Musculoskelet Disord. 2023 Jun 2;24(1):443
     
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    Articles:
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    Changes in foot posture evaluated with dynamic pedobarography over the course of childhood in ambulatory youth with cerebral palsy
    Chris Church, Nancy Lennon, Madison Lennon, John D Henley, Thomas Shields, Tim Niiler, Daveda A Taylor, M Wade Shrader, and Freeman Miller
    Journal of Children’s Orthopaedics 2024, Vol. 18(1) 3 –12
     
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    Articles:
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    Reliability of a Photo-Based Modified Foot Posture Index (MFPI) in Quantifying Severity of Foot Deformity in Children With Cerebral Palsy
    Georgiadis, Andrew G. MD et al
    Journal of Pediatric Orthopaedics ():10.1097/BPO.0000000000002812, September 11, 2024. | DOI: 10.1097/BPO.0000000000002812
     
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    News Release 19-Nov-2024
    Changing the definition of cerebral palsy


    In the United States, there are currently more adults living with cerebral palsy than children.
    Despite this, the Centers for Disease Control and Prevention still label cerebral palsy as “the most common motor disability in childhood.”

    This definition not only ignores cerebral palsy as a lifelong condition but contributes to a lopsided research focus directed only at pediatric care and not care into adulthood and across the lifespan, experts say.

    University of Michigan Health’s Mark Peterson, Ph.D., M.S., FACSM, a professor of physical medicine and rehabilitation, has been working to make sure the definition of cerebral palsy is changed so that as more children with cerebral palsy grow to be adults, their care can continue to be consistent.

    In a perspective piece published in the New England Journal of Medicine, Peterson lays out the rationale behind this paradigm shift.

    Discrepancies in care for cerebral palsy
    Adults with cerebral palsy face large gaps in care when they move away from pediatrics, and it’s often described as “falling off a cliff.”

    Since cerebral palsy has historically been classified as a pediatric condition, those with cerebral palsy find that there’s a lack of knowledge about how to treat the factors that come with their condition as they age.

    “The vast difference in care can leave many adults with cerebral palsy with low confidence that they will be able to receive the care they need or have their concerns heard,” said Peterson.

    “As pediatric patients, many living with cerebral palsy may find themselves feeling confident that their questions would have answers and their care needs, such as physical therapy, would always be covered by insurance. When their care transitions to adult providers, many find that their insurance no longer covers their needs, and their providers are unable to answer questions about aspects of their condition that are changing as they age.”

    Common risks for adults with cerebral palsy can include the early onset of secondary conditions such as osteoporosis, hypertension, diabetes and psychiatric disorders.
    Peterson explains it’s important to address these comorbidities to ensure patients receive proper treatment.

    Most standards of care for adults with cerebral palsy are carried over from pediatrics, says Peterson, focusing on individual body parts and addressing issues such as spasticity, joint contractures, pain and musculoskeletal disorders, leaving no standard of care for adults.

    “This means that people with cerebral palsy may develop other noncommunicable diseases in early adulthood that can contribute to accelerated aging and premature death,” said Peterson.

    Creating a new definition for cerebral palsy
    As more children with cerebral palsy grow up to become adults, groups like the Cerebral Palsy Foundation, the Weinberg Family Cerebral Palsy Center, the Cerebral Palsy Research Network and the Cerebral Palsy Alliance Research Foundation have adopted a new definition for cerebral palsy that they hope becomes widely used and accepted.

    The new definition defines cerebral palsy as “the most common lifelong physical disability” people can face.

    “This new definition acknowledges that cerebral palsy is lifelong and doesn’t end after childhood,” said Peterson.

    “Robust operational definitions with language like this help drive accurate research about the correct subject group. There is research needed specifically about adults with cerebral palsy and the impact that this lifelong condition has. Having a more accurate definition helps guide that research.”
    Adding that there are unique physical challenges impacting those with cerebral palsy as they age creates opportunities for considering it, and other childhood-onset neurodevelopmental conditions, in studies that focus on adults and include adults with cerebral palsy that may otherwise be excluded.

    “Being able to have adults with cerebral palsy participate in more clinical research will contribute immensely to our understanding of the natural history of cerebral palsy as people age,” said Peterson.
    “This can range from cerebral palsy specific studies to any study that involves neurodevelopmental conditions. The information that is gathered will help improve the care adults with cerebral palsy receive and better tailor their treatments.”

    Clear definitions about cerebral palsy and its lifelong impact also play a crucial role in public health surveillance.

    For instance, a proper operational definition from the National Institutes of Health can enable more accurate national surveillance and coordinated responses to health threats by being more specific about how the threat will impact those with cerebral palsy.


    These definitions can also inform policy decisions regarding resource allocation, reimbursement, and quality-improvement initiatives, shaping the delivery of healthcare services.

    As adults with cerebral palsy age, Peterson explains that many age out of the resources they had covered before when being seen in pediatrics.

    Reframing the definition could also help adjust the policies that support and cover care for adults with the disease.

    The NIH has reported, roughly, a15% increase in cerebral palsy-related funding since 2017, yet funding for life-course-based initiatives remains insufficient.

    “For a long time, the goal of medical advancements with cerebral palsy was to make sure the children with cerebral palsy were able to become healthy adults. Now, it’s time to make sure we are properly treating the adults we worked to care for as children.”
     
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